Crop protection, Food, Feed and Flavor Chemicals

4-OXODECANEDIOATE
4-Oxodecanedioate is an organic dicarboxylic acid.
4-Oxodecanedioate is a naturally occurring dicarboxylic acid with the chemical formula (CH2)8(CO2H)2.
4-Oxodecanedioate is a white flake or powdered solid.

CAS Number: 111-20-6
EC Number: 203-845-5
Chemical Formula: HOOC(CH₂)₈COOH
Molar Mass: 202.25 g/mol

4-Oxodecanedioate is a naturally occurring dicarboxylic acid with the chemical formula HO2C(CH2)8CO2H.
4-Oxodecanedioate is a white flake or powdered solid.

Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to its use in the manufacture of candles.
4-Oxodecanedioate is a derivative of castor oil.

In the industrial setting, 4-Oxodecanedioate and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
4-Oxodecanedioate can be used as a surfactant in the lubricating oil industry to increase the antirust properties of lubricating oils on metals.

4-Oxodecanedioate is a white granular powder.
4-Oxodecanedioate has Melting point of 153 °F.
4-Oxodecanedioate is Slightly soluble in water.

4-Oxodecanedioate is a white granular powder.
Melting point of 4-Oxodecanedioate is 153 °F.

4-Oxodecanedioate is slightly soluble in water.
Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to 4-Oxodecanedioate is use in the manufacture of candles.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
4-Oxodecanedioate has a role as a human metabolite and a plant metabolite.

4-Oxodecanedioate was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to 4-Oxodecanedioate is use in the manufacture of candles.
4-Oxodecanedioate sublimes slowly at 750 mmHg when heated to melting point.

4-Oxodecanedioate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 tonnes per annum.
4-Oxodecanedioate is a urinary metabolite that has been identified as an anti-fatigue biomarker.

In 4-Oxodecanedioate's purest form, 4-Oxodecanedioate is a powdered crystal or white flaky substance.
In 4-Oxodecanedioate's pure state 4-Oxodecanedioate is a white flake or powdered crystal.
4-Oxodecanedioate is described as non-hazardous, though in its powdered form 4-Oxodecanedioate can be prone to flash ignition (a typical risk in handling fine organic powders).

Sebaceus is Latin for tallow candle, sebum (tallow) is Latin for tallow, and refers to its use in the manufacture of candles.
4-Oxodecanedioate is white flaky crystals.
4-Oxodecanedioate is slightly soluble in water, soluble in alcohol and ether.

4-Oxodecanedioate is also the raw material for the production of alkyd resins (used as surface coatings, plasticized nitrocellulose coatings, and urea resin varnishes) and polyurethane rubber, cellulose resins, vinyl resins, and synthetic rubber plasticizers, softeners, and solvents.
4-Oxodecanedioate’s a naturally occurring dicarboxylic acid that is non-hazardous, though 4-Oxodecanedioate can be vulnerable to flash ignition in its powder form.

One of the most common uses for 4-Oxodecanedioate is in the manufacturing of candles.
4-Oxodecanedioate sublimes slowly at 750 mm Hg when heated to melting point.;DryPowder; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals;Solid;WHITE POWDER WITH CHARACTERISTIC ODOUR.

4-Oxodecanedioate also shows up in the industrial industry, being used as a monomer and intermediate for various products and materials.
4-Oxodecanedioate is white flaky crystal.
4-Oxodecanedioate is slightly soluble in water, soluble in alcohol and ether.

4-Oxodecanedioate is a derivative of castor oil, with the vast majority of world production occurring in China which annually exports over 20,000 metric tonnes, representing over 90 % of global trade of the product.
4-Oxodecanedioate is produced from castor oil.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
4-Oxodecanedioate is a conjugate acid of a sebacate(2-) and a sebacate.

4-Oxodecanedioate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 tonnes per annum.
4-Oxodecanedioate’s mostly colorless but can be a light shade of yellow.

4-Oxodecanedioate is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
4-Oxodecanedioate is a normal urinary acid.

4-Oxodecanedioate is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
4-Oxodecanedioate is a normal urinary acid.

4-Oxodecanedioate is an acid derived from castor oil.
4-Oxodecanedioate is sold in the form of a white, granular powder and sometimes referred to by either of 4-Oxodecanedioate is chemical names: 1,8-octanedicarboxylic acid.

4-Oxodecanedioate is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
4-Oxodecanedioate also has a mild odor to it, though nothing that stands out.

There are two ways that 4-Oxodecanedioate can be produced: castor oil and adipic acid.
4-Oxodecanedioate is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
4-Oxodecanedioate’s far more common for 4-Oxodecanedioate to be derived from castor oil, as the process is green and cost effective.

To make the 4-Oxodecanedioate, the castor oil is heated to high temperatures with alkali.
4-Oxodecanedioate was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
4-Oxodecanedioate is a white granular powder.

The purity of 4-Oxodecanedioate is based on the type of reaction it has.
Generally, modern conversion technology leads to a purer product.
4-Oxodecanedioate's Melting point is 153°F.

4-Oxodecanedioate is slightly soluble in water.
4-Oxodecanedioate is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.

4-Oxodecanedioate belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

4-Oxodecanedioate is made from castor oil and belongs to the homologous series of dicarboxylic acids.
The best known application of 4-Oxodecanedioate is the production of polyamides.

4-Oxodecanedioate, a dicarboxylic acid with structure (HOOC) (CH2)8(COOH), is a naturally occurring chemical derivative of castor oil which has been proven safe in vivo.
4-Oxodecanedioate is a normal urinary acid.

4-Oxodecanedioate is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.
4-Oxodecanedioate is a natural C10 liquid fatty acid, directly produced from castor oil.

4-Oxodecanedioate is found to be associated with carnitine-acylcarnitine translocase deficiency and medium chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism.
4-Oxodecanedioate is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.

4-Oxodecanedioate is a normal urinary acid.
4-Oxodecanedioate is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.

4-Oxodecanedioate was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
4-Oxodecanedioate and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

4-Oxodecanedioate has a role as a human metabolite and a plant metabolite.
4-Oxodecanedioate is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.

4-Oxodecanedioate is a conjugate acid of a sebacate(2-) and a sebacate.
4-Oxodecanedioate derives from a hydride of a decane.

4-Oxodecanedioate acts as a plasticizer, solvent and softener.
4-Oxodecanedioate is a white flake or powdered solid.

Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to its use in the manufacture of candles.
4-Oxodecanedioate is manufactured by splitting of castor oil followed by fusion with caustic.

4-Oxodecanedioate sublimes slowly at 750 mmHg when heated to melting point.
4-Oxodecanedioate is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.

4-Oxodecanedioate is white crystalline powder or granular form slightly dissolves in water, completely dissolves in ethanol or ether but not in benzene.
4-Oxodecanedioate is high end derivative of castor oil and 4-Oxodecanedioate is also called "Sebacic Acid".

4-Oxodecanedioate's Melting point is 153 °F.
4-Oxodecanedioate is slightly soluble in water.

4-Oxodecanedioate is a derivative of castor oil.
4-Oxodecanedioate is a white granular powder.

4-Oxodecanedioate is a natural liquid fatty acid, directly produced from castor oil.
4-Oxodecanedioate is a derivative of castor oil.

4-Oxodecanedioate is an organic dicarboxylic acid.
4-Oxodecanedioate is a naturally occurring dicarboxylic acid with the chemical formula (CH2)8(CO2H)2.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
4-Oxodecanedioate has a role as a human metabolite and a plant metabolite.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
4-Oxodecanedioate is a conjugate acid of a sebacate(2-) and a sebacate.

4-Oxodecanedioate derives from a hydride of a decane.
4-Oxodecanedioate is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.

4-Oxodecanedioate is a saturated, straight-chain naturally occurring dicarboxylic acid with 10 carbon atoms.
4-Oxodecanedioate is a normal urinary acid.

In patients with multiple acyl-CoA-dehydrogenase deficiency (MADD) or glutaric aciduria type II (GAII) are a group of metabolic disorders due to deficiency of either electron transfer flavoprotein or electron transfer flavoprotein ubiquinone oxidoreductase, biochemical data shows an increase in urine 4-Oxodecanedioate excretion.
4-Oxodecanedioate is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.

4-Oxodecanedioate was named from the Latin sebaceus (tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles.
4-Oxodecanedioate is a dicarboxylic acid obtained from the dry distillation of castor oil.

4-Oxodecanedioate is derived from castor oil.
Two molecules are needed to obtain a castor 4-Oxodecanedioate.
Castor oil is obtained from the fruit seed of castor (Ricinus communis L.) a large shrub that grows mainly in India, Brazil and China.

The seed has an oil content of 40-50%.
4-Oxodecanedioate is solid at room temperature and melts above 130°C.

4-Oxodecanedioate is in the form of white crystalline solid (powder or granules depending of the manufacturer).
Stabilizer in alkyd resins, maleic and other polyesters, polyurethanes, fibers, paints, candles and perfumes, low temperature lubricants and hydraulic fluids.

4-Oxodecanedioate derives from a hydride of a decane.
4-Oxodecanedioate is a naturally occurring dicarboxylic acid which is a derivative of castor oil.

4-Oxodecanedioate is a white flake or powdered crystal slightly soluble in water that has been proposed as an alternative energy substrate in total parenteral nutrition.
4-Oxodecanedioate is a dicarboxylic acid with structure (HOOC)(CH2)8(COOH), and is naturally occurring.

Uses of 4-Oxodecanedioate:
4-Oxodecanedioate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
4-Oxodecanedioate is used in the synthesis of polyamide and alkyd resins.

4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics and painting materials.
In the industrial setting, 4-Oxodecanedioate and its homologues such as azelaic acid can be used in plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics, and painting materials.
4-Oxodecanedioate is used in the following products: washing & cleaning products, adhesives and sealants, fuels, lubricants and greases, coating products and fertilisers.

Release to the environment of 4-Oxodecanedioate can occur from industrial use: of substances in closed systems with minimal release.
Release to the environment of 4-Oxodecanedioate can occur from industrial use: of substances in closed systems with minimal release.

4-Oxodecanedioate also works as a buffering & neutralizing agent.
Other release to the environment of 4-Oxodecanedioate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

4-Oxodecanedioate is used in skin care, hair care and sun care formulations.
4-Oxodecanedioate is used as a topical emollient.

4-Oxodecanedioate and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
4-Oxodecanedioate is used in the synthesis of polyamide and alkyd resins.

4-Oxodecanedioate can be used as a corrosion inhibitor in metalworking fluids and as a complexing agent in greases.

Release to the environment of 4-Oxodecanedioate can occur from industrial use: formulation of mixtures and in the production of articles.
Other release to the environment of 4-Oxodecanedioate is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).
4-Oxodecanedioate can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones) and leather (e.g. gloves, shoes, purses, furniture).

4-Oxodecanedioate is used in the following products: biocides (e.g. disinfectants, pest control products), pH regulators and water treatment products, laboratory chemicals, plant protection products, water softeners and water treatment chemicals.
4-Oxodecanedioate is used in the following areas: formulation of mixtures and/or re-packaging and agriculture, forestry and fishing.

4-Oxodecanedioate is used for the manufacture of: chemicals.
Other release to the environment of 4-Oxodecanedioate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

4-Oxodecanedioate is used in the following products: adhesives and sealants, polymers, coating products, lubricants and greases and cosmetics and personal care products.
In the industrial setting, 4-Oxodecanedioate and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

4-Oxodecanedioate is a urinary metabolite that has been identified as an anti-fatigue biomarker.
4-Oxodecanedioate and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
4-Oxodecanedioate is used in the synthesis of polyamide and alkyd resins.

Release to the environment of 4-Oxodecanedioate can occur from industrial use: formulation of mixtures, in processing aids at industrial sites, as processing aid, as an intermediate step in further manufacturing of another substance (use of intermediates), for thermoplastic manufacture, manufacturing of the substance and formulation in materials.

4-Oxodecanedioate can be used as plasticizers for plastics and cold-resistant rubber, as well as for polyamide, polyurethane, alkyd resin, synthetic lubricating oil, lubricating oil additives, spices, coatings, cosmetics, etc.
4-Oxodecanedioate is used in the following products: laboratory chemicals, water treatment chemicals, pH regulators and water treatment products, water softeners and polymers.

4-Oxodecanedioate is widely used in the preparation of 4-Oxodecanedioate esters, such as dibutyl sebacate, dioctyl sebacate, diisooctyl sebacate.
4-Oxodecanedioate is used in the following areas: formulation of mixtures and/or re-packaging.

4-Oxodecanedioate and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics and painting materials.

4-Oxodecanedioate is used as source material for various products.
In addition, 4-Oxodecanedioate is used as a crosslinker in the adhesives industry, as a plasticizer in the plastics industry, as a component of lubricants and as an extender in packaging films.

4-Oxodecanedioate is used for the manufacture of: chemicals, plastic products and rubber products.
4-Oxodecanedioate can be used as a synthesis intermediate for sebacates esters which can be used as emollients, masking agent, film forming agent, hair or skin conditioning agent, SPF Booster, etc.

Release to the environment of 4-Oxodecanedioate can occur from industrial use: in processing aids at industrial sites, in the production of articles, formulation of mixtures, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid and for thermoplastic manufacture.
4-Oxodecanedioate can also be used as raw material for producing nylon 1010, nylon 910, nylon 810, nylon 610, nylon 9 and high temperature resistant lubricating oil diethylhexyl ester.

4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics and painting materials.
Release to the environment of 4-Oxodecanedioate can occur from industrial use: manufacturing of the substance.
In the industrial setting, 4-Oxodecanedioate and its homologues such as azelaic acid can be used as a monomer for nylon 610, plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.

4-Oxodecanedioate can be used as a surfactant in the lubricating oil industry to increase the antirust properties of lubricating oils on metals.
4-Oxodecanedioate is used in the following products: washing & cleaning products, adhesives and sealants, fuels, lubricants and greases, coating products and fertilisers.

4-Oxodecanedioate and its derivatives such as azelaic acid have a variety of industrial uses as plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc.
4-Oxodecanedioate is used in the synthesis of polyamide and alkyd resins.

4-Oxodecanedioate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics and painting materials.

Sebaceus is Latin for tallow candle, and sebum is Latin for tallow. These terms refer to the use of 4-Oxodecanedioate in the manufacturing of candles.
In particular, 4-Oxodecanedioate is used as a thickener in lithium complex grease.

In addition, 4-Oxodecanedioate can be used as an intermediate in the production of aromatics, antiseptics and painting materials as well as in the synthesis of polyamide and alkyd resins.
4-Oxodecanedioate is also used in the synthesis of polyamide, as nylon, and of alkyd resins.

But as stated above, 4-Oxodecanedioate has a lot of uses for the industrial setting.
4-Oxodecanedioate's anti-corrosive properties make 4-Oxodecanedioate a useful addition to metalworking fluids and antifreeze.

4-Oxodecanedioate is also an additive and thickener for grease and lubricants, as well as an intermediate in paints and other coatings.
When used in a mixture with other dibasic acids 4-Oxodecanedioate is especially effective as a ferrous corrosion inhibitor for metalworking fluids, engine coolants, metal cleaners, aqueous hydraulic fluids.

4-Oxodecanedioate can also be used as a complexing agent for lithium complex grease which will increase dropping point and improve mechanical stability.
Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

4-Oxodecanedioate is used as a raw material for alkyd and polyester resins, plasticizers, polyester rubbers, and polyamide synthetic fibers.
4-Oxodecanedioate can be used as a monomer for nylon, lubricants, hydraulic fluids, cosmetics, plasticizers and more.

4-Oxodecanedioate can also be used as an intermediate for antiseptics, aromatics and painting products.
4-Oxodecanedioate is used in the synthesis of polyamide and alkyd resins.

4-Oxodecanedioate is also used as an intermediate for aromatics, antiseptics and painting materials.
4-Oxodecanedioate is used as a stabilizer in alkyd resins, maleic and other polyesters, polyurethanes, and fibers.

4-Oxodecanedioate is also used in paint products, candles, perfumes, low temperature lubricants, and hydraulic fluids, and to make nylon.
4-Oxodecanedioate is largely used in the manufacturing process of Nylon 6-10.

An isomer, iso4-Oxodecanedioate, has several applications in the manufacture of vinyl resin plasticizers, extrusion plastics, adhesives, ester lubricants, polyesters, polyurethane resins and synthetic rubber.
4-Oxodecanedioate can also be found in plasticizers, lubricants, hydraulic fluids, cosmetics, and candle manufacturing.

In cosmetics, 4-Oxodecanedioate can be used as a buffering ingredient for pH adjustment or a chemical intermediate in the synthesis of various esters.
Do4-Oxodecanedioate is mainly used in top-grade powder coatings and paint, adhesives, pulp & paper, chemical and industrial facilities, surfactants, antiseptics.

In combination with Amine, 4-Oxodecanedioate is used to produce engineering plastics polyamide resins wich is a high performance nylon 6-12, adhesives, diester synthetic lubricants, fibers, curatives, plasticizers, polyester coatings, epoxy resins.
Due to 4-Oxodecanedioate's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

4-Oxodecanedioate was historically used in candle-making and today has many functions in manufacturing and industrial processing.
Some of the principal uses of 4-Oxodecanedioate include acting as an intermediate in nylon, synthetic resins and other plastics.
4-Oxodecanedioate and its derivatives, as azelaic acid, have a variety of industrial uses as plasticizers, lubricants, diffusion pump oils, cosmetics, candles, etc.

Lubricants, Plastics and Greases use:
The fatty acids in castor oil give 4-Oxodecanedioate excellent lubricating properties.
You can choose either traditional castor oil or Jamaican black castor oil as a lubricant in metal drawing and other industrial processes.

Such as:
Plasticizers
Lubricants
Hydraulic Fluids
Cosmetics
Candles
Buffering
pH Regulating Agent
pH Adjuster
Adhesives & Sealants
Paints & Coatings
Personal Care Products

Metalworking Fluids uses:
Due to 4-Oxodecanedioate's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

Such as:
Polymers
Plasticizers
Lubricants
Corrosion inhibitors

4-Oxodecanedioate has been used in the synthesis of:
biodegradable and elastomeric polyesters [poly(glycerol sebacate)]
novel bio-nylon, PA5.10
novel temperature-response hydrogel based on poly(ether-ester anhydride) nanoparticle for drug-delivery applications

Common Uses for 4-Oxodecanedioate:
Sebaceus is Latin for tallow candle, and sebum is Latin for tallow.
These terms refer to the use of 4-Oxodecanedioate in the manufacturing of candles.
But as stated above, 4-Oxodecanedioate has a lot of uses for the industrial setting.

4-Oxodecanedioate can be used as a monomer for nylon, lubricants, hydraulic fluids, cosmetics, plasticizers and more.
4-Oxodecanedioate can also be used as an intermediate for antiseptics, aromatics and painting products.

Applications of 4-Oxodecanedioate:

Major Applications:
Our 4-Oxodecanedioate offers a competitve solution in many applications:

To produce polymers:
In industry: to produce plasticizers, lubricants, and corrosion retardants
In cosmetics: as buffering ingredient or as a chemical intermediate to produce a wide range of esters

Cosmetic applications:
Our 4-Oxodecanedioate can be used directly in cosmetics formulation as a pH corrector (buffering).
In this case, the main applications are skin care (mainly face/neck care), and color cosmetics.
The 4-Oxodecanedioate is also widely used as a synthesis intermediate to produce sebacates esters such as DIPS or DIS (diisopropyl sebacate), DOS (diethylhexyl sebacate), DES (diethyl sebacate) and DBS (dibutyl sebacate).

These sebacate are used as: emollient, solvent, plasticizer, masking (reducing or inhibiting the basic odour of the product), film forming, hair or skin conditioning.
Generally, sebacate esters are claimed to enable a good penetration, give a non-oily and silky skin feel.
These esters are also recognized to be good pigment dispersant (DOS), be good sun protection factor (SPF) booster (DIPS blended), and prevent whitening in antiperspirant (DIPS).

Plasticizers applications:
The 4-Oxodecanedioate (DC 10), is widely used to produce a various range of plastics, and brings to those plastics a bio-based part

Case, Metalworking Fluids and Plastics:
Due to 4-Oxodecanedioate's smoothing and conditioning properties, Jamaican black castor oil is ideal for use in products like cleansers, moisturizers, and ethnic hair care products.

Lubricants and Greases:
The fatty acids in castor oil give 4-Oxodecanedioate excellent lubricating properties.
You can choose either traditional castor oil or Jamaican black castor oil as a lubricant in metal drawing and other industrial processes.

Characteristics of 4-Oxodecanedioate:

Acme-Hardesty 4-Oxodecanedioate is refined to a minimum 99.5-percent purity.
4-Oxodecanedioate has a minimum acid value of 550, a maximum ash content of 0.03 percent and a maximum moisture level of 0.20 percent.

4-Oxodecanedioate's melting point is between 131.0 and 134.5°C.
Some of the principal uses of 4-Oxodecanedioate include acting as an intermediate in nylon, synthetic resins and other plastics.

4-Oxodecanedioate's anti-corrosive properties make it a useful addition to metalworking fluids and antifreezes.
4-Oxodecanedioate is also an additive and thickener for grease and lubricants, as well as an intermediate in paints and other coatings.

Benefits of 4-Oxodecanedioate:
In cosmetic products, 4-Oxodecanedioate can act as a pH corrector.
In plastics, 4-Oxodecanedioate can be used to provide better flexibility and lower melting temperature.

For lubricants and anti-corrosion applications, 4-Oxodecanedioate is used to produce a salt derivative that can be used as a coolant for aircraft, automotive and truck engines.

Here are the attributes that make 4-Oxodecanedioate as flexible as it is.
Excellent lubricity
Low temperature fluidity
Higher thermal stability
High flash points
Low pour points

Key Benefits:
In cosmetic products, 4-Oxodecanedioate can act as a pH corrector.
In plastics, 4-Oxodecanedioate can be used to provide better flexibility and lower melting temperature.
For lubricants and anti-corrosion applications, 4-Oxodecanedioate is used to produce a salt derivative that can be used as a coolant for aircraft, automotive and truck engines.

The attributes that make 4-Oxodecanedioate as flexible as it is:
Excellent lubricity
Low temperature fluidity
Higher thermal stability
High flash points
Low pour points

Alternative Parents of 4-Oxodecanedioate:
Dicarboxylic acids and derivatives
Carboxylic acids
Organic oxides
Hydrocarbon derivatives
Carbonyl compounds

Substituents of 4-Oxodecanedioate:
Medium-chain fatty acid
Dicarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Compound Type of 4-Oxodecanedioate:
Animal Toxin
Cosmetic Toxin
Food Toxin
Industrial/Workplace Toxin
Metabolite
Natural Compound
Organic Compound
Plasticizer

Preparation of 4-Oxodecanedioate:
4-Oxodecanedioate is normally made from castor oil, which is essentially glycerol triricinoleate.
The castor oil is heated with sodium hydroxide at about 250°e.

This treatment results in saponification of the castor oil to ricinoleic acid which is then cleaved to give 2-octanol and 4-Oxodecanedioate:
This process results in low yields of 4-Oxodecanedioate (about 50% based on the castor oil) but, nevertheless, other routes have not proved competitive.
4-Oxodecanedioate is a colourless crystalline solid, m.p. 134℃.

The Main Method of Preparation:
(1) Castor oil is as raw material, ricinoleate is separated from castor oil, with the condition of inflating and 280~300℃, caustic soda proceeds alkali fusion and the reaction is heated for 10h, sebum acid sodium salt can obtain, deputy product is 2-octanol.
The sodium salt is dissolved in water, adding sulfuric acid to neutralize, after bleaching, the solution is cooled to precipitate sebum acid, 4-Oxodecanedioate is washed with cold water, and finally recrystallized.

CH3 (CH2) 5CH (OH) CH2CH = CH (CH2) 7COOH +
2NaOH → CH3 (CH2) 5CH (OH) CH3 + NaOOC (CH2) 8COONa + H2
NaOOC (CH2) 3COONa + H2SO4 → HOOC (CH2) 8COOH + Na2SO4

(2) Adipic acid (hexane diacid) is as raw material to synthesize.
Adipic acid and methanol can proceed esterification reaction to form dimethyl adipate, ion exchange membrane proceeds electrolytic oxidation to get dimer, i.e., dimethyl sebacate, and then reacts with sodium hydroxide to form the disodium salt, hydrochloric acid (or sulfuric acid) is used to neutralize and 4-Oxodecanedioate can obtain.

Production of 4-Oxodecanedioate:
4-Oxodecanedioate is produced from castor oil by cleavage of ricinoleic acid, which is obtained from castor oil.
Octanol & glycerin is a byproduct.
4-Oxodecanedioate can also be obtained from decalin via the tertiary hydroperoxide, which gives cyclodecenone, a precursor to 4-Oxodecanedioate.

4-Oxodecanedioate is produced from castor oil by cleavage of ricinoleic acid, which is obtained from castor oil.
Octanol & glycerin is a byproduct.

4-Oxodecanedioate can also be obtained from decalin via the tertiary hydroperoxide, which gives cyclodecenone, a precursor to 4-Oxodecanedioate.
Almost all of the current industrial production of 4-Oxodecanedioate is using castor oil as raw material.

Castor oil cracking method:
Castor oil is heated under the action of alkali hydrolysis to generate ricinoleic acid sodium soap, and then add sulfuric acid to generate ricinoleic acid; in the presence of diluent cresol, add alkali heated to 260-280 ℃ for cracking to generate 4-Oxodecanedioate double sodium salt and secoctanol and hydrogen, cracked material diluted by water, heated and neutralized with acid, the double sodium salt into a monosodium salt; and then boiled with acid after decolorization of activated carbon neutralization solution.
The monosodium salt of 4-Oxodecanedioate is turned into 4-Oxodecanedioate crystals, and then separated and dried to obtain the finished product.

Potential Medical Significance of 4-Oxodecanedioate:
Sebum is a secretion by skin sebaceous glands.
4-Oxodecanedioate is a waxy set of lipids composed of triglycerides (≈41%), wax esters (≈26%), squalene (≈12%), and free fatty acids (≈16%).[4][5]

Included in the free fatty acid secretions in sebum are polyunsaturated fatty acids and 4-Oxodecanedioate.
4-Oxodecanedioate is also found in other lipids that coat the skin surface.
Human neutrophils can convert 4-Oxodecanedioate to its 5-oxo analog, i.e., 5-oxo-6E,8Z-octadecenoic acid, a structural analog of 5-oxo-eicosatetraenoic acid and like this oxo-eicosatetraenoic acid is an exceptionally potent activator of eosinophils, monocytes, and other pro-inflammatory cells from humans and other species.

This action is mediated by the OXER1 receptor on these cells.
4-Oxodecanedioate is suggested that 4-Oxodecanedioate is converted to its 5-oxo analog during, and thereby stimulates pro-inflammatory cells to contribute to the worsening of, various inflammatory skin conditions.

Purification Methods of 4-Oxodecanedioate:
Purify 4-Oxodecanedioate via the disodium salt which, after crystallisation from boiling water (charcoal), is again converted to the free acid.
The free acid is crystallised repeatedly from hot distilled water or from Me2CO/pet ether and dried under vacuum.

Properties of 4-Oxodecanedioate:
4-Oxodecanedioate has high purity.
4-Oxodecanedioate is 100% of vegetal origin.

4-Oxodecanedioate has linear chain.
4-Oxodecanedioate has granules or powder forms.

4-Oxodecanedioate has high reactivity to produce a wide range of esters.
4-Oxodecanedioate Sublimes slowly at 750 mmHg when heated to melting point.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.
4-Oxodecanedioate has a role as a human metabolite and a plant metabolite.

4-Oxodecanedioate is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid.
4-Oxodecanedioate is a conjugate acid of a sebacate(2-) and a sebacate.

4-Oxodecanedioate derives from a hydride of a decane.
4-Oxodecanedioate is a natural product found in Isatis tinctoria, Euglena gracilis, and other organisms with data available.

Handling and Storage of 4-Oxodecanedioate:

Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Storage class (TRGS 510):
8A: Combustible, corrosive hazardous materials

Stability and Reactivity of 4-Oxodecanedioate:

Reactivity:
4-Oxodecanedioate reacts exothermically to neutralize bases, both organic and inorganic.
4-Oxodecanedioate may react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt.

4-Oxodecanedioatean reacts with active metals to form gaseous hydrogen and a metal salt.
Such reactions are slow in the dry, but systems may absorb enough water from the air to allow corrosion of iron, steel, and aluminum parts and containers.

Reacts slowly with cyanide salts to generate gaseous hydrogen cyanide.
Reacts with solutions of cyanides to cause the release of gaseous hydrogen cyanide.

Chemical stability:
Stable under recommended storage conditions.

Incompatible materials:

Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:

Waste treatment methods:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.

Contaminated packaging:
Dispose of as unused product

First Aid Measures of 4-Oxodecanedioate:

General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.

Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.

In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures of 4-Oxodecanedioate:

Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

Special hazards arising from the substance or mixture:
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.

Accidental release measures of 4-Oxodecanedioate:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Exposure Controls/Personal Protection of 4-Oxodecanedioate:

Control parameters:

Components with workplace control parameters:

Contains no substances with occupational exposure limit values.

Exposure controls:

Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:

Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.

Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested: Dermatril (KCL 740 / Aldrich Z677272, Size M)

Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested: Dermatril (KCL 740 / Aldrich Z677272, Size M)

4-Oxodecanedioate should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.

Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).

Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Identifiers of 4-Oxodecanedioate:
CAS number, 111-20-6
EC number, 203-845-5
Hill Formula, C₁₀H₁₈O₄
Chemical formula, HOOC(CH₂)₈COOH
Molar Mass, 202.25 g/mol
HS Code, 2917 13 10
Boiling point, 295 °C (133 hPa)
Density, 1.210 g/cm3 (20 °C)
Melting Point, 133 - 137 °C
Vapor pressure, 1 hPa (183 °C)
Bulk density, 600 - 620 kg/m3
Solubility, 1 g/l
Assay (GC, area%), ≥ 98.0 % (a/a)
Melting range (lower value), ≥ 131 °C
Melting range (upper value), ≤ 134 °C
Identity (IR), passes test

PSA: 74.60000
XLogP3: 2.1
Appearance: White powder
Density: 1.231 g/cm3
Melting Point: 130.8 °C
Boiling Point: 294.5 °C
Flash Point: 220 °C
Refractive Index: 1.422
Water Solubility:
Solubility in water, g/100ml: 0.1 (poor)
Storage Conditions:
Storage Room low temperature ventilation drying
Vapor Pressure: 1.24E-06mmHg at 25°C

Properties of 4-Oxodecanedioate:
XLogP3: 2.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 9
Exact Mass: 202.12050905 g/mol
Monoisotopic Mass: 202.12050905 g/mol
Topological Polar Surface Area: 74.6Ų
Heavy Atom Count: 14
Complexity: 157
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Molecular Weight: 202.25 g/mol
Chemical formula, C10H18O4
Molar mass, 202.250 g•mol−1
Density, 1.209 g/cm3
Melting point, 131 to 134.5 °C (267.8 to 274.1 °F; 404.1 to 407.6 K)
Boiling point, 294.4 °C (561.9 °F; 567.5 K) at 100 mmHg
Solubility in water, 0.25 g/L
Acidity (pKa), 4.720, 5.450

Melting Point, 131°C to 134°C
Density, 1.271
Boiling Point, 295°C (100mmHg)
Flash Point, 220°C (428°F)
Linear Formula, HO2C(CH2)8CO2H
Quantity, 100 g
Beilstein, 1210591
Merck Index, 14,8415
Solubility Information, Slightly soluble in water.
Formula Weight, 202.25
Percent Purity, ≥98%
Chemical Name or Material: 4-Oxodecanedioate

Density: 1.1±0.1 g/cm3
Boiling Point: 374.3±0.0 °C at 760 mmHg
Melting Point: 133-137 °C(lit.)
Molecular Formula: C10H18O4
Molecular Weight: 202.247
Flash Point: 198.3±19.7 °C
Exact Mass: 202.120514
PSA: 74.60000
LogP: 1.86
Vapour Pressure: 0.0±1.8 mmHg at 25°C
Index of Refraction: 1.475
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, bases, reducing agents.
Water Solubility: 1 g/L (20 ºC)
4-Tertiary Butyl Catechol
cas no: 4420-74-0 3-(Trimethoxysilyl)-1-propanethiol; 1-Propanethiol, 3-(trimethoxysilyl)-; gamma-Mercaptopropyltrimethoxysilane; (3-Thiopropyl)trimethoxysilane; 3-Mercaptopropyltrimethoxysilane; 1-Propanethiol, 3-(trimethoxysilyl)-;
5-METHYL-2-HEXANONE
5-Methyl-2-hexanone is a colorless stable liquid with a pleasant odor.
5-Methyl-2-hexanone is provides low density, low surface tension and a high boiling point.
5-Methyl-2-hexanone is used for special purpose coatings, OEM coatings and coatings for automotive plastics.

CAS Number: 110-12-3
EC Number: 203-737-8
Molecular Formula: C7H14O
Molecular Weight (g/mol): 114.188

5-Methyl-2-hexanone is found in animal foods.
5-Methyl-2-hexanone is a volatile component in fruit pulp of papaya (Carica papaya), black tea aroma and in cooked beef and egg aroma 5-Methyl-2-hexanone belongs to the family of Ketones.
These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be H).

5-Methyl-2-hexanone is a ketone.
5-Methyl-2-hexanone is a natural product found in Solanum lycopersicum and Zingiber officinale with data available.

5-Methyl-2-hexanone is a colorless stable liquid with a pleasant odor.
5-Methyl-2-hexanone is slightly soluble in water and miscible with most organic solvents.
5-Methyl-2-hexanone has high solvent activity and a slow evaporation rate with low surface tension.

5-Methyl-2-hexanone is used for applications such as industrial coatings, resin solvents, thinners, polymerization solvents, and rubber intermediates.

5-Methyl-2-hexanone is acts as a very good solvent for high-solids coatings.
5-Methyl-2-hexanone is offers high solvent activity and slow evaporation rate.

5-Methyl-2-hexanone is provides low density, low surface tension and a high boiling point.
5-Methyl-2-hexanone is used for special purpose coatings, OEM coatings and coatings for automotive plastics.

5-Methyl-2-hexanone is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
5-Methyl-2-hexanone is used by consumers, by professional workers (widespread uses), in formulation or re-packing and at industrial sites.

5-Methyl-2-hexanone has high solvent activity, slow evaporation rate, low density, low surface tension, and a high boiling point.
These properties make 5-Methyl-2-hexanone a very good solvent for high-solids coatings.
Because regulations limit the weight of solvent per gallon of coating, formulators favor the use of low-density solvents that help reduce the VOC content of a coating.

5-Methyl-2-hexanone is lower in density than ester, aromatic hydrocarbons, and glycol ether solvents with similar evaporation rates.
The low density and high activity of 5-Methyl-2-hexanone are significant advantages when formulating low-viscosity, high-solids coatings.
In addition, 5-Methyl-2-hexanone is useful as a polymerization solvent for high solids acrylic resins.

5-Methyl-2-hexanone belongs to the class of organic compounds known as ketones.
These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom).

Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
5-Methyl-2-hexanone is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.

Thus, 5-Methyl-2-hexanone is considered to be an oxygenated hydrocarbon lipid molecule.
5-Methyl-2-hexanone has been detected, but not quantified, in a few different foods, such as eggs, fruits, and tea.
This could make 5-Methyl-2-hexanone a potential biomarker for the consumption of these foods.

The Global 5-Methyl-2-hexanone Market 2022-2026:
The Global 5-Methyl-2-hexanone Market is expected to reach a CAGR of 5.0% during the forecast period.
The growth in this market can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

5-Methyl-2-hexanone is a clear, colorless liquid with a characteristic, fruity odor.
It is miscible in water and has a boiling point of 151°C.

5-Methyl-2-hexanone is produced by the condensation of acetone and isobutanol.
5-Methyl-2-hexanone finds application as a solvent in paints & coatings, process solvents, and automotive industries among others.

On the basis of Application, the market is segmented into paints & Coatings, Process Solvents, Automotive.

Paints & Coatings:
5-Methyl-2-hexanone is used as an ingredient in the manufacturing of alkyd resins, which are extensively used in the paints & coatings industry.
5-Methyl-2-hexanone acts as a reactant in the production of polyurethanes, unsaturated polyesters, and other resins.
5-Methyl-2-hexanone also finds application as a coalescing agent and thinner in paint formulations.

Process Solvents:
5-Methyl-2-hexanone is used as a solvent in the production of resins, gums, cellulose esters, and lacquers.
5-Methyl-2-hexanone is also used as an extraction solvent for oils & fats.
5-Methyl-2-hexanone finds application in the textile industry as 5-Methyl-2-hexanone helps in the dyeing and printing of textiles.

Automotive:
5-Methyl-2-hexanone is used as a solvent in the automotive industry.
5-Methyl-2-hexanone is used in the production of lacquers, resins, and gums.
5-Methyl-2-hexanone is also used as an extraction solvent for oils & fats as well as in the textile industry.

On the basis of region, the market is segmented into North America, Latin America, Europe, Asia Pacific, and Middle East & Africa.

The market in North America is expected to grow at the highest CAGR during the forecast period.
The growth in this region can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

Latin America is expected to be the second-largest market for 5-Methyl-2-hexanone during the forecast period.
The growth in this region can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

The market in Europe is expected to grow at a moderate CAGR during the forecast period.
The growth in this region can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

The market in the Asia Pacific is expected to grow at a significant CAGR during the forecast period.
The growth in this region can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

The market in the Middle East & Africa is expected to grow at a moderate CAGR during the forecast period.
The growth in this region can be attributed to the increasing demand for 5-Methyl-2-hexanone from various end-use industries such as paints & coatings, process solvents, automotive, and others.

Research Report offers a comprehensive analysis of the market, providing valuable insights into the market status, size, share, SWOT and PESTLE analysis.
The report examines the market growth potential, opportunities, drivers, industry-specific challenges, and risks, along with emerging trends and recent developments.

With an extensive table of content, tables and figures, the report covers crucial information on the consumption of 5-Methyl-2-hexanone by country, including forecasted data up to 2026.
Furthermore, the report presents a segmentation analysis by types, applications, manufacturers, and geographical regions, providing an overview of the market dynamics and current market situation.

Market Analysis and Insights: Global 5-Methyl-2-hexanone Market:
5-Methyl-2-hexanone has high solvent activity, slow evaporation rate, low density, low surface tension, and a high boiling point. These properties make 5-Methyl-2-hexanone a very good solvent for high-solids coatings.
Because regulations limit the weight of solvent per gallon of coating, formulators favor the use of low-density solvents that help reduce the VOC content of a coating.

5-Methyl-2-hexanone is lower in density than ester, aromatic hydrocarbons, and glycol ether solvents with similar evaporation rates.
The low density and high activity of 5-Methyl-2-hexanone are significant advantages when formulating low-viscosity, high-solids coatings.

In addition, 5-Methyl-2-hexanone is useful as a polymerization solvent for high solids acrylic resins.
The global Keyword market is valued at USD million in 2020 is expected to reach USD million by the end of 2026, growing at a CAGR of during 2021-2026.

This report focuses on Keyword volume and value at the global level, regional level and company level.
From a global perspective, this report represents overall Keyword market size by analysing historical data and future prospect.

Regionally, this report focuses on several key regions: North America, Europe, China and Japan etc. research report includes specific segments by Type and by Application.
This study provides information about the sales and revenue during the historic and forecasted period of 2015 to 2026.
Understanding the segments helps in identifying the importance of different factors that aid the market growth.

Drivers and Restraints:
The research report has incorporated the analysis of different factors that augment the market’s growth.
5-Methyl-2-hexanone constitutes trends, restraints, and drivers that transform the market in either a positive or negative manner.

This section also provides the scope of different segments and applications that can potentially influence the market in the future.
The detailed information is based on current trends and historic milestones.

This section also provides an analysis of the volume of production in the global market for each type from 2017 to 2026.
This section mentions the volume of production by region from 2017 to 2026.
Pricing analysis is included in the report according to each type from the year 2017 to 2026, manufacturer from 2017 to 2022, the region from 2017 to 2022, and global price from 2017 to 2026.

A thorough evaluation of the restraints included in the report portrays the contrast to drivers and gives room for strategic planning.
Factors that overshadow the market growth are pivotal as they can be understood to devise different bends for getting hold of the lucrative opportunities that are present in the ever-growing market. Additionally, insights into market experts’ opinions have been taken to understand the market better.

Segment Analysis:
The research report includes specific segments by region (country), by manufacturers, by Type and by Application.
Each type provides information about production during the forecast period of 2017 to 2026.

By Application segment also provides consumption during the forecast period of 2017 to 2026.
Understanding the segments helps in identifying the importance of different factors that aid market growth.

Uses of 5-Methyl-2-hexanone:
5-Methyl-2-hexanone is used as a solvent for nitrocellulose, cellulose acetate, butyrate, acrylics, high-solid coatings, and vinyl copolymers.
5-Methyl-2-hexanone is used in manufacture of rubber antioxidants, in paints, lacquers and varnishes.

5-Methyl-2-hexanone is solvent for nitrocellulose, cellulose acetate, butyrate, acrylics, and vinyl copolymers.
5-Methyl-2-hexanone is used as a solvent for the production of high-solids coatings.

Widespread uses by professional workers:
5-Methyl-2-hexanone is used in the following products: coating products, fillers, putties, plasters, modelling clay and laboratory chemicals.
5-Methyl-2-hexanone is used in the following areas: building & construction work.
Other release to the environment of 5-Methyl-2-hexanone is likely to occur from: indoor use as processing aid and outdoor use as processing aid.

Uses at industrial sites:
5-Methyl-2-hexanone is used in the following products: coating products and fillers, putties, plasters, modelling clay.
5-Methyl-2-hexanone is used in the following areas: building & construction work.

5-Methyl-2-hexanone is used for the manufacture of: chemicals.
Release to the environment of 5-Methyl-2-hexanone can occur from industrial use: in processing aids at industrial sites and as an intermediate step in further manufacturing of another substance (use of intermediates).

Industry Uses:
Paint additives and coating additives not described by other categories
Sealant (barrier)
Solvent

Consumer Uses:
5-Methyl-2-hexanone is used in the following products: coating products, adhesives and sealants and fillers, putties, plasters, modelling clay.
Other release to the environment of 5-Methyl-2-hexanone is likely to occur from: indoor use as processing aid and outdoor use as processing aid.

Other Consumer Uses:
Not Known or Reasonably Ascertainable
Paint additives and coating additives not described by other categories

Industrial Processes with risk of exposure:
Painting (Solvents)

Applications of 5-Methyl-2-hexanone:
Auto OEM
Auto refinish
General industrial coatings
Paints & coatings
Process solvents

Key Attributes of 5-Methyl-2-hexanone:
Excellent solvent activity
High dilution ratio
Inert - Nonfood use
Low density
Low surface tension
Non-HAP
Non-SARA
REACH compliant
Readily biodegradable
Slow evaporation rate
Urethane grade

General Manufacturing Information of 5-Methyl-2-hexanone:

Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
Fabricated Metal Product Manufacturing
Miscellaneous Manufacturing
Paint and Coating Manufacturing

Human Metabolite Information of 5-Methyl-2-hexanone:

Cellular Locations:
Cytoplasm
Extracellular

Handling and Storage of 5-Methyl-2-hexanone:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling 5-Methyl-2-hexanone must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do 5-Methyl-2-hexanone without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Storage Conditions:
Store in tightly closed containers in a cool, well ventilated area away from sources of oxidizers (such as perchlorates, peroxides, permanganates, chlorates, and nitrates), strong oxidizers (such as chlorine, bromine, and fluorine), reducing agents, and aldehydes.
Sources of ignition such as smoking and open flames are prohibited where 5-Methyl-2-hexanone is handled, used or stored.

Metal containers involving the transfer of 5 gallons or more of 5-Methyl-2-hexanone should be grounded and bonded.
Drums must be equipped with self-closing valves, pressure vacuum bungs, and flame arresters.

Reactivity Profile of 5-Methyl-2-hexanone:
Ketones, such as 5-Methyl-2-hexanone, are reactive with many acids and bases liberating heat and flammable gases (e.g., H2).
The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone.

Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat.
Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides.
They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

First Aid Measures of 5-Methyl-2-hexanone:

Eye:
IRRIGATE IMMEDIATELY - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids.
Get medical attention immediately.

Skin:
SOAP FLUSH PROMPTLY - If this chemical contacts the skin, promptly flush the contaminated skin with soap and water.
If this chemical penetrates the clothing, promptly remove the clothing and flush the skin with water.
If irritation persists after washing, get medical attention.

Breathing:
RESPIRATORY SUPPORT - If a person breathes large amounts of this chemical, move the exposed person to fresh air at once.
If breathing has stopped, perform artificial respiration.

Keep the affected person warm and at rest.
Get medical attention as soon as possible.

Swallow:
MEDICAL ATTENTION IMMEDIATELY - If this chemical has been swallowed, get medical attention immediately.

Fire Fighting of 5-Methyl-2-hexanone:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

For fire involving UN1170, UN1987 or UN3475, alcohol-resistant foam should be used.
Ethanol (UN1170) can burn with an invisible flame.
Use an alternate method of detection (thermal camera, broom handle, etc.).

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto 5-Methyl-2-hexanone.
If it can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn.
Use AFFF, alcohol-resistant foam, powder, carbon dioxide.

In case of fire:
Keep drums, etc., cool by spraying with water.

Fire Fighting Procedures:

If material on fire or involved in fire:
Do not extinguish fire unless flow can be stopped or safely confined.
Use water in flooding quantities as fog.

Solid streams of water may be ineffective.
Cool all affected containers with flooding quantities of water.

Apply water from as far a distance as possible.
Use alcohol foam, dry chemical or carbon dioxide.
Keep run-off water out of sewers and water sources.

Accidental Release Measures of 5-Methyl-2-hexanone:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Spillage Disposal of 5-Methyl-2-hexanone:

Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of 5-Methyl-2-hexanone.
Collect leaking liquid in sealable containers.

Absorb remaining liquid in sand or inert absorbent.
Then store and dispose of according to local regulations.
Do NOT wash away into sewer.

Cleanup Methods of 5-Methyl-2-hexanone:
Evacuate and restrict persons not wearing protective equipment from area of spill or leak until cleanup is complete.
Remove all ignition sources.

Establish forced ventilation to keep levels below explosive limit.
Absorb liquids in vermiculite, dry sand, earth, peat, carbon, or similar material and deposit in sealed containers.

Keep this chemical out of a confined space because of the possibility of an explosion.
5-Methyl-2-hexanone may be necessary to contain and dispose of this chemical as a hazardous waste.

If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters.
Contact your Department of Environmental Protection or your regional office of the federal EPA for specific recommendations.
If employees are required to clean up spills, they must be properly trained and equipped.

Environmental considerations -- land spill:
Dig a pit, pond, lagoon, holding area to contain liquid or solid material.
If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner.

Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete.
Absorb bulk liquid with fly ash, cement powder, or commercial sorbents.

Environmental considerations -- water spill:
Use natural barriers or oil spill control booms to limit spill travel.
Remove trapped material with suction hoses.

Environmental considerations -- air spill:
Apply water spray or mist to knock down vapors.

Disposal Methods of 5-Methyl-2-hexanone:
The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination.
Recycle any unused portion of 5-Methyl-2-hexanone for 5-Methyl-2-hexanone approved use or return 5-Methyl-2-hexanone to the manufacturer or supplier.

Ultimate disposal of the chemical must consider:
5-Methyl-2-hexanone's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

The following wastewater treatment technologies have been investigated for 5-Methyl-2-hexanone:
Activated carbon.

Preventive Measures of 5-Methyl-2-hexanone:
Do not breathe gas, fumes, vapor, or spray.
The scientific literature for the use of contact lenses in industry is conflicting.

The benefit or detrimental effects of wearing contact lenses depend not only upon 5-Methyl-2-hexanone, but also on factors including the form of 5-Methyl-2-hexanone, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses.
However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye.

In those specific cases, contact lenses should not be worn.
In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area.
Ventilation control of the contaminant as close to 5-Methyl-2-hexanone point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants.

If material not on fire and not involved in fire:
Keep sparks, flames, and other sources of ignition away.
Keep material out of water sources and sewers.

Build dikes to contain flow as necessary.
Attempt to stop leak if without undue personnel hazard.
Use water spray to knock down vapors.

Identifiers of 5-Methyl-2-hexanone:
CAS: 110-12-3
Molecular Formula: C7H14O
Molecular Weight (g/mol): 114.188
MDL Number: MFCD00008950
InChI Key: FFWSICBKRCICMR-UHFFFAOYSA-N
PubChem CID: 8034
IUPAC Name: 5-methylhexan-2-one
SMILES: CC(C)CCC(=O)C

CAS: 110-12-3
Molecular Formula: C7H14O
Molecular Weight: 114.19

Linear Formula: (CH3)2CHCH2CH2COCH3
CAS Number: 110-12-3
Molecular Weight: 114.19

EC / List no.: 203-737-8
CAS no.: 110-12-3
Mol. formula: C7H14O

CAS number: 110-12-3
EC index number: 606-026-00-4
EC number: 203-737-8
Hill Formula: C₇H₁₄O
Molar Mass: 114.19 g/mol
HS Code: 2914 19 10

Synonym(s): 5-Methyl-2-hexanone, 5-Methyl-2-hexanone, Isoamyl methyl ketone
Empirical Formula (Hill Notation): C7H14O
CAS Number: 110-12-3
Molecular Weight: 114.19
MDL number: MFCD00008950
EC Index Number: 203-737-8

Properties of 5-Methyl-2-hexanone:
Physical description: Colorless, clear liquid with a pleasant, fruity odor.
Boiling point: 291°F:
Molecular weight: 114.2
Freezing point/melting point: -101°F
Vapor pressure: 5 mmHg
Flash point: 97°F
Specific gravity: 0.81:
Ionization potential: 9.284 eV
Lower explosive limit (LEL): 1% at 200°F
Upper explosive limit (UEL): 8.2% at 200°F
NFPA health rating: 1
NFPA fire rating: 3
NFPA reactivity rating: 0

Molecular Formula: C7H14O
Molar Mass: 114.19
Density: 0.814 g/mL at 25 °C (lit.)
Melting Point: -74 °C
Boling Point: 145 °C (lit.)
Flash Point: 106°F
Water Solubility: 5.4 g/L (20 ºC)
Solubility: water: soluble5.4g/L at 25°C
Vapor Presure: 4.5 mm Hg ( 20 °C)
Vapor Density: 3.94 (vs air)
Appearance: Liquid
Color: Clear colorless
Exposure Limit: TLV-TWA 240 mg/m3 (50 ppm) (ACGIH).
BRN: 506163
Storage Condition: Store below +30°C.
Explosive Limit: 1.35-8.2%, 93°F
Refractive Index: n20/D 1.406(lit.)

Boiling point: 144 °C (1013 hPa)
Density: 0.81 g/cm3 (20 °C)
Explosion limit: 1.4 %(V)
Flash point: 40 °C
Ignition temperature: 455 °C
Melting Point: -73.9 °C
Vapor pressure: 6 hPa (20 °C)
Solubility: 5.4 g/l

Vapor pressure: 5.3 hPa ( 20 °C)
Quality Level: 200
Assay: ≥98% (GC)
Form: liquid
Autoignition temp.: 455 °C

Potency:
3200 mg/kg LD50, oral (Rat)
8100 mg/kg LD50, skin (Rabbit)

Expl. lim.: 1.4 % (v/v)
bp: 144 °C/1013 hPa
mp: -74 °C
Transition temp: flash point 43 °C
Solubility: 5.4 g/L
Density: 0.81 g/cm3 at 20 °C
Storage temp.: 2-30°C
InChI: 1S/C7H14O/c1-6(2)4-5-7(3)8/h6H,4-5H2,1-3H3
InChI key: FFWSICBKRCICMR-UHFFFAOYSA-N

Molecular Weight: 114.19
XLogP3: 1.9
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 3
Exact Mass: 114.104465066
Monoisotopic Mass: 114.104465066
Topological Polar Surface Area: 17.1 Ų
Heavy Atom Count: 8
Complexity: 74.5
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of 5-Methyl-2-hexanone:
Melting Point: -74°C
Color: Colorless
Boiling Point: 144°C
UN Number: 2302
Quantity: 25 mL
Formula Weight: 114.19
Percent Purity: ≥98.0% (GC)
Physical Form: Liquid
Chemical Name or Material: Isoamyl Methyl Ketone

Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 0.811 - 0.813
Identity (IR): passes test

Related Products of 5-Methyl-2-hexanone:
N,N-Dimethyl-L-histidine Methyl Ester
1,5-Dimethylhexylamine
(2,5-Dimethylphenyl)boronic Acid
2,3-Dimethylphenylboronic Acid
2-(2,6-Dimethyl-3-hydroxyphenyl)-3-oxo-2-azaindolizidine

Names of 5-Methyl-2-hexanone:

Regulatory process names:
2-Hexanone, 5-methyl-
2-Methyl-5-hexanone
5-Methyl-2-hexanone
5-methylhexan-2-one
5-METHYLHEXAN-2-ONE
5-Methylhexan-2-one
5-methylhexan-2-one
5-methylhexan-2-one; isoamyl methyl ketone
Isoamyl methyl ketone
isoamyl methyl ketone
Isopentyl methyl ketone
Ketone, methyl isoamyl
Methyl isoamyl ketone
Methyl isopentyl ketone
MIAK

Translated names:
5-methylhexaan-2-on (nl)
5-methylhexan-2-on (cs)
5-methylhexan-2-on (da)
5-Methylhexan-2-on (de)
5-metil-2-heksanon (sl)
5-metil-2-heksanonas (lt)
5-metil-heksan-2-on (hr)
5-metilesan-2-one (it)
5-metilheksanons-2 (lv)
5-metilhexan-2-ona (es)
5-metilhexan-2-ona (ro)
5-metilhexano-2-ona (pt)
5-metilhexán-2-on (hu)
5-metyl-2-heksanon (no)
5-metyl-2-hexanon (sv)
5-metylheksan-2-on (no)
5-metylhexan-2-on (sv)
5-metylhexán-2-ón (sk)
5-metyloheksan-2-on (pl)
5-metyyli-2-heksanoni (fi)
5-metyyliheksan-2-oni (fi)
5-metüülheksaan-2-oon (et)
5-méthylhexan-2-one; isoamylméthylcétone (fr)
5-μεθυλεξαν-2-όν (el)
5-мeтилхексан-2-oн (bg)
isoamylmethylketon (cs)
Isoamylmethylketone (de)
Isoamüülmetüülketoon (et)
izoamil metil keton (sl)
izoamil metil ketona (ro)
izoamil-metil-keton (hr)
izoamil-metil-keton (hu)
izoamilmetilketonas (lt)
izoamilmetilketons (lv)
izopentyl(metyl)ketón (sk)
keton izopentylowo-metylowy (pl)
keton metylowo-izoamylowy (pl)
metilisoamilcetona (pt)
metyloizoamyloketon (pl)
изоамил метил кетон (bg)

CAS name:
2-Hexanone, 5-methyl-

IUPAC names:
2-Hexanone, 5-methyl-
5-methyl hexan-2-one
5-Methyl-2-hexanon
5-Methylhexan-2-one
5-methylhexan-2-one
5-methylhexan-2-one
Isoamyl Methyl Ketone
isoamyl methyl ketone
METHYL ISOAMYL KETONE
Methyl isoamyl ketone

Trade names:
5-methylhexan-2-one
MIAK

Other identifiers:
110-12-3
606-026-00-4

Synonyms of 5-Methyl-2-hexanone:
5-METHYL-2-HEXANONE
110-12-3
5-Methylhexan-2-one
2-Hexanone, 5-methyl-
Isoamyl methyl ketone
Isopentyl methyl ketone
Methyl isoamyl ketone
MIAK
2-Methyl-5-hexanone
Ketone, methyl isoamyl
Methyl isopentyl ketone
Isobutylacetone
(CH3)2CHCH2CH2COCH3
3-Methylbutyl methyl ketone
DTXSID5021914
CHEBI:88432
6O4A4A5F28
5-Methyl-2-hexanone, 99%
DTXCID801914
CAS-110-12-3
HSDB 2885
5-Methyl-hexan-2-one
EINECS 203-737-8
UN2302
BRN 0506163
UNII-6O4A4A5F28
methylisoamyl ketone
MFCD00008950
2-hexanone-5-methyl
methyl iso-amyl ketone
EC 203-737-8
SCHEMBL35996
4-01-00-03329 (Beilstein Handbook Reference)
CHEMBL45354
5-Methylhexan-2-one [UN2302] [Flammable liquid]
METHYL-2-HEXANONE, 5-
Methyl Isoamyl Ketone Reagent Grade
ZINC2041073
Tox21_201346
Tox21_302906
5-METHYL-2-HEXANONE [HSDB]
LMFA12000037
AKOS000119819
UN 2302
NCGC00249030-01
NCGC00256572-01
NCGC00258898-01
DB-040899
FT-0620609
I0087
EN300-19620
J-517759
Q2152381
5-Methylhexan-2-one [UN2302] [Flammable liquid]
5-Methyl-2-hexanone [ACD/IUPAC Name]
(CH3)2CHCH2CH2COCH3 [Formula]
110-12-3 [RN]
203-737-8 [EINECS]
2-Hexanone, 5-methyl- [ACD/Index Name]
5-Methyl-2-hexanon [German] [ACD/IUPAC Name]
5-Méthyl-2-hexanone [French] [ACD/IUPAC Name]
5-Methylhexan-2-one
6O4A4A5F28
Isobutylacetone
isopentyl methyl ketone
methyl isoamyl ketone
MFCD00008950 [MDL number]
MIAK
MP3850000
[110-12-3] [RN]
203-737-8MFCD00008950
2-hexanone-5-methyl
3-Methylbutyl methyl ketone
4-01-00-03329 (Beilstein Handbook Reference) [Beilstein]
5-METHYL-2-HEXA
5-METHYL-2-HEXANONE|5-METHYLHEXAN-2-ONE
5-Methyl-hexan-2-one
EINECS 203-737-8
Isoamyl Methyl Ketone
ketone, isopentyl methyl
Ketone, methyl isoamyl
Methyl iso-amyl ketone
Methyl isoamyl ketone, Isoamyl methyl ketone
Methyl isopentyl ketone
UN 2302
UNII:6O4A4A5F28
UNII-6O4A4A5F28
MIAK
Isobutylaceton
methyl-2-hexanone
5-Methyl-2-hexanone
5-methylhexan-2-one
Isoamylmethylketone
ketone,methylisoamyl
Methyl isoamyl ketone
Isopentyl-methylketon
methylisopentylketone
Isoamyl methyl ketone
Ketone, methyl isoamyl
Methyl isopentyl ketone
(1R)-2-bromo-1-phenylethanol
Isopentyl methyl ketone~Methyl isoamyl ketone~MIAK
AA/AMPS
Acrylic Acid-2-Acrylamido-2-Methylpropane Sulfonic Acid Copolymer; AA-AMPSA; Acrylic Acid-2-Acrylamido-2-Methylpropane Sulfonic Acid Copolymer; Sulfonated Polyacrylic Acid Copolymer; 2-acrylamido-2-methylpropanesulfonic acid-acrylic acid copolymer; 2-Propenoic acid polymer with 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid; Sulfonated Polyacrylic Acid Copolymer; ACRYLIC ACID /ACRYLAMIDOMETHYL PROPANE SULFONIC ACID COPOLYMER; AcrylicAcid-AMPSCopolymer(AA/AMPS); Acrylic Acid-2-Acrylamido-2-Methylpropane Sulfonic Acid Copolymer; AA/AMPS; Acrylic acid-2-acrylamido-2-methyl propyl sulfonic acid copolymer; 2-Propenoic acid,polymer with 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid; prop-2-enoic acid - 2-(acryloylamino)butane-2-sulfonic acid (1:1) CAS NO:40623-75-4
ACAI BERRY EXTRACT

Acai Berry Extract is a natural, potent antioxidant-rich ingredient derived from the Acai palm tree, known for its high content of vitamins, minerals, and essential fatty acids.
Acai Berry Extract is recognized for its ability to protect the skin from environmental stressors, support healthy skin aging, and enhance skin radiance, making it a popular choice in skin care formulations.
This versatile extract offers both protective and rejuvenating benefits, helping to maintain youthful and vibrant skin.

CAS Number: 11028-42-5
EC Number: 234-241-9

Synonyms: Acai Berry Extract, Euterpe Oleracea Fruit Extract, Acai Pulp Extract, Acai Palm Extract, Acai Fruit Extract, Acai Antioxidant Extract, Acai Berry Skin Care, Acai Berry Antioxidant Complex, Acai Fruit Oil Extract, Acai Berry Concentrate, Acai Extract, Acai Powder Extract, Acai Fruit Juice Extract, Acai Berry Active, Acai Phytoextract, Acai Berry Phytocomplex, Acai Bioactive Extract, Acai Natural Extract, Acai Berry Oil, Acai Berry Essence



APPLICATIONS


Acai Berry Extract is extensively used in the formulation of anti-aging creams, providing powerful antioxidant protection that helps to reduce the appearance of fine lines and wrinkles.
Acai Berry Extract is favored in the creation of serums, where it delivers concentrated antioxidant benefits that enhance skin radiance and reduce oxidative stress.
Acai Berry Extract is utilized in the development of moisturizing creams, offering hydration and protection for dry and mature skin.

Acai Berry Extract is widely used in the production of brightening treatments, helping to even skin tone and improve luminosity.
Acai Berry Extract is employed in the formulation of sunscreens, providing additional protection against UV-induced damage while enhancing overall skin resilience.
Acai Berry Extract is essential in the creation of facial oils, offering a blend of nourishing and protective benefits that enhance skin health and vitality.

Acai Berry Extract is utilized in the production of body lotions, offering all-over antioxidant protection and promoting skin firmness and elasticity.
Acai Berry Extract is a key ingredient in the formulation of after-sun products, providing soothing and protective benefits to sun-exposed skin.
Acai Berry Extract is used in the creation of protective serums, where it strengthens the skin's natural defenses against environmental aggressors.

Acai Berry Extract is applied in the formulation of face masks, providing intensive antioxidant care that revitalizes and refreshes the skin.
Acai Berry Extract is employed in the production of eye creams, providing targeted antioxidant care that reduces puffiness, dark circles, and signs of aging around the eyes.
Acai Berry Extract is used in the development of anti-pollution skincare products, providing a protective barrier against environmental pollutants while enhancing skin radiance.

Acai Berry Extract is widely utilized in the formulation of scalp treatments, providing antioxidant protection that supports scalp health and promotes stronger hair.
Acai Berry Extract is a key component in the creation of anti-inflammatory skincare products, offering soothing and protective benefits for sensitive skin.
Acai Berry Extract is used in the production of lip care products, providing antioxidant protection and hydration for soft, smooth lips.

Acai Berry Extract is employed in the formulation of prebiotic skincare products, supporting the skin’s microbiome while providing powerful antioxidant benefits.
Acai Berry Extract is applied in the creation of hand creams, offering antioxidant protection that helps to maintain skin softness and reduce signs of aging on the hands.
Acai Berry Extract is utilized in the development of daily wear creams, offering balanced hydration, protection, and anti-aging benefits for everyday use.

Acai Berry Extract is found in the formulation of skin repair treatments, providing intensive care that helps to restore and protect damaged or aging skin.
Acai Berry Extract is used in the production of facial mists, offering a refreshing boost of antioxidant protection throughout the day.
Acai Berry Extract is a key ingredient in the creation of soothing gels, providing antioxidant care that calms and protects sensitive skin.

Acai Berry Extract is widely used in the formulation of multipurpose balms, providing versatile care for sensitive areas such as lips, hands, and face.
Acai Berry Extract is employed in the development of nourishing body butters, offering rich hydration and antioxidant protection for dry, rough skin.
Acai Berry Extract is applied in the production of anti-aging serums, offering deep antioxidant protection that helps to maintain youthful-looking skin.

Acai Berry Extract is utilized in the creation of facial oils, offering nourishing care that supports skin health and reduces oxidative stress.
Acai Berry Extract is found in the formulation of sensitive skin repair treatments, providing targeted care for areas prone to irritation and discomfort.
Acai Berry Extract is used in the production of sun care products, providing protection against UV rays while offering antioxidant care that preserves skin health.



DESCRIPTION


Acai Berry Extract is a natural, potent antioxidant-rich ingredient derived from the Acai palm tree, known for its high content of vitamins, minerals, and essential fatty acids.
Acai Berry Extract is recognized for its ability to protect the skin from environmental stressors, support healthy skin aging, and enhance skin radiance, making it a popular choice in skin care formulations.

Acai Berry Extract offers additional benefits such as enhancing skin resilience and improving overall skin texture, ensuring long-lasting protection and radiance.
Acai Berry Extract is often incorporated into formulations designed to provide comprehensive protection against environmental damage, offering both immediate and long-term benefits.
Acai Berry Extract is recognized for its ability to enhance the overall health and appearance of the skin, leaving it smooth, vibrant, and youthful-looking.

Acai Berry Extract is commonly used in both traditional and innovative skincare formulations, providing a reliable solution for protecting and preserving skin health.
Acai Berry Extract is valued for its ability to support the skin's natural defenses, making it a key ingredient in products that aim to protect the skin from environmental aggressors.
Acai Berry Extract is a versatile ingredient that can be used in a variety of products, including creams, serums, oils, and lotions.

Acai Berry Extract is an ideal choice for products targeting aging, stressed, and environmentally exposed skin, as it provides gentle yet effective protection and rejuvenation.
Acai Berry Extract is known for its compatibility with other skincare actives, allowing it to be easily integrated into multi-functional formulations.
Acai Berry Extract is often chosen for formulations that require a balance between protection, rejuvenation, and skin care, ensuring comprehensive care for all skin types.

Acai Berry Extract enhances the overall effectiveness of personal care products by providing powerful antioxidant protection, skin-enhancing effects, and environmental defense in one ingredient.
Acai Berry Extract is a reliable ingredient for creating products that offer a pleasant user experience, with noticeable improvements in skin health, radiance, and resilience.
Acai Berry Extract is an essential component in innovative skincare products that stand out in the market for their performance, safety, and ability to protect and enhance the skin.



PROPERTIES


Chemical Formula: N/A (Natural extract)
Common Name: Acai Berry Extract (Euterpe Oleracea Fruit Extract)
Molecular Structure:
Appearance: Dark purple to black liquid or powder
Density: Approx. 1.02-1.05 g/cm³ (for liquid extract)
Melting Point: N/A (liquid or powder form)
Solubility: Soluble in water and alcohols; insoluble in oils
Flash Point: >100°C (for liquid extract)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low (for liquid extract)



FIRST AID


Inhalation:
If Acai Berry Extract is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of eye contact, flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
If Acai Berry Extract is ingested, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of vapors.

Ventilation:
Ensure adequate ventilation when handling large amounts of Acai Berry Extract to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Acai Berry Extract.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Acai Berry Extract in a cool, dry, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid inhalation of vapors and direct contact with skin and eyes.
Use explosion-proof equipment in areas where vapors may be present.


Storage:

Temperature:
Store Acai Berry Extract at temperatures between 15-25°C as recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Acai Berry Extract away from incompatible materials, including strong oxidizers.

Handling Equipment:
Use dedicated equipment for handling Acai Berry Extract to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of cosmetic ingredients.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

Acai Yeşilçay Ekstraktı
Green Tea (Camellia sinensis) Extract; camellia sinensis leaf extract; extract of the leaves of the tea, camellia sinensis, theaceae; GREEN TEA EXTRACT; camellia thea leaf extract; claritea; denoxyline; earl grey tea kiinote organic (Omega); extract of the leaves of the tea, camellia sinensis, theaceae; tea leaf extract; thea assamica leaf extract;thea sinensis leaf extract cas no:84650-60-2
ACCELERATOR NL-65-100
Accelerator NL-65-100 is a high-reactive amine accelerator used for curing unsaturated polyesters at ambient temperatures.
Accelerator NL-65-100 is used in pultrusion, resin transfer molding, filament winding, hand lay-up and spray-up applications.
The radical formation, which is necessary to start the polymerization reaction, is at ambient temperatures with most generally applied organic peroxides too slow.

CAS: 99-97-8
MF: C9H13N
MW: 135.21
EINECS: 202-805-4

Synonyms
N,N,4-TRIMETHYLBENZENAMINE;N,N-DIMETHYL-4-METHYLANILINE;N,N-DIMETHYL-4-TOLUIDINE;N,N-DIMETHYL-PARA-TOLUIDINE;N,N-DIMETHYL-P-TOLUIDINE;Benzeneamine,N,N,4-trimethyl-;dimethyl-4-toluidine;Dimethyl-p-toluidine;N,N-Dimethyl-p-toluidine;99-97-8;N,N,4-TRIMETHYLANILIN;Dimethyl-p-toluidine;Benzenamine, N,N,4-trimethyl-;Dimethyl-4-toluidine;N,N-Dimethyl-4-methylaniline;N,N,4-Trimethylbenzenamine;p-Methyl-N,N-dimethylaniline;p-(Dimethylamino)toluene;N,N-Dimethyl-p-tolylamine;4-Dimethylaminotoluene;N,N-Dimethyl-para-toluidine;p-Toluidine, N,N-dimethyl-;NSC 1785;p,N,N-Trimethylaniline;Dimetil-p-toluidina;N,N-Dimethyl-4-toluidine;dimethyltolylamine;1-(Dimethylamino)-4-methylbenzene;4,N,N-Trimethylaniline;S8XC5939VU;DTXSID0021832;NSC-1785;NL 65-100;DTXCID401832;p-N,N-Trimethylaniline;CAS-99-97-8;Dimetil-p-toluidina [Italian];CCRIS 1001;EINECS 202-805-4;UNII-S8XC5939VU;Benzeneamine,N,N,4-trimethyl-;HSDB 8202;MFCD00008316;N,4-Trimethylaniline;dimethyl-(p-tolyl)-amine;EC 202-805-4;Benzenamine,N,4-trimethyl-;SCHEMBL28378;MLS001050174;4-dimethylamino-1-methylbenzene;4,N,N-Trimethylaniline, 99%;CHEMBL1462714;N,N-Dimethyl-p-methylphenylamine;NSC1785;Tox21_201370;Tox21_300062;AC-368;AKOS015915159;N,N-DIMETHYL-P-TOLUIDINE [IARC];NCGC00091397-01;NCGC00091397-02;NCGC00091397-03;NCGC00254201-01;NCGC00258922-01;SMR001216586;D0807;NS00002247;E75885;EN300-7266829;4,N,N-Trimethylaniline, purum, >=98.0% (GC);Q2051705;W-100002;Z1002998236

Accelerator NL-65-100 is an organic compound.
Accelerator NL-65-100 is commonly used as a catalyst and curing agent in various chemical processes, including the production of polymers, resins, and adhesives.
Additionally, Accelerator NL-65-100 finds application as a component in dental materials, such as dental composites and adhesives.
Accelerator NL-65-100's ability to initiate and accelerate curing reactions, coupled with its low toxicity and stability, makes it a valuable additive in industries ranging from plastics and coatings to healthcare and dentistry.
To speed up the radical formation in a controllable way, organic peroxides must therefore be used in combination with a so-called accelerator.
The shelf life of Accelerator NL-65-100 is 9 months.
Accelerator NL-65-100 is listed in TSCA.

Accelerator NL-65-100 Chemical Properties
Melting point: -25°C
Boiling point: 211 °C(lit.)
Density: 0.937 g/mL at 25 °C(lit.)
Vapor density: >1 (vs air)
Vapor pressure: 0.1 hPa (20 °C)
Refractive index: n20/D 1.546(lit.)
Fp: 182 °F
Storage temp.: Store below +30°C.
Solubility: 0.65g/l
Form: Liquid
pka: pK1:7.24(+1) (25°C)
Color: Clear yellow
Explosive limit: 7%
Water Solubility: Miscible with alcohol, ether and chloroform. Immiscible with water.
BRN: 774409
Dielectric constant: 3.3(20℃)
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: GYVGXEWAOAAJEU-UHFFFAOYSA-N
LogP: 1.729-2.81 at 35℃
CAS DataBase Reference: 99-97-8(CAS DataBase Reference)
IARC: 2B (Vol. 115) 2018
EPA Substance Registry System: Accelerator NL-65-100 (99-97-8)

Applications
Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.
Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.
Accelerator NL-65-100 reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Further, Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.

The curing of unsaturated polyester resins at ambient temperatures can in general not be performed by an organic peroxide alone.
The radical formation, which is necessary to start the polymerisation reaction, is at ambient temperatures with most generally applied organic peroxides too slow.
To speed up the radical formation in a controllable way, organic peroxides must therefore be used in combination with a so-called accelerator.

Reactivity Profile
Accelerator NL-65-100 neutralizes acids in exothermic reactions to form salts plus water.
May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.
May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death.
Contact with molten substance may cause severe burns to skin and eyes.
Avoid any skin contact.
Effects of contact or inhalation may be delayed.
Fire may produce irritating, corrosive and/or toxic gases.
Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Synthesis
Accelerator NL-65-100 was prepared by reacting p-toluidine with methanol and POCl3 in autoclave heated up to 280° C for 3h.
Reflux for 3hours with 2 molar equivalents of Ac2O, then fractionally distil Accelerator NL-65-100 under reduced pressure.
Alternatively, dry Accelerator NL-65-100 over BaO, distil and store Accelerator NL-65-100 over KOH.
The picrate has m 128o (from EtOH).
Methods described for Accelerator NL-65-100 are applicable here.
ACCELERATOR NL-65-100
Accelerator NL-65-100 is a high-reactive amine accelerator used for curing unsaturated polyesters at ambient temperatures.
Accelerator NL-65-100 is miscible with alcohol, ether and chloroform.
Accelerator NL-65-100 is immiscible with water.


CAS Number: 99-97-8
EC Number: 202-805-4
Chemical Composition: N,N-Dimethyl p-toluidine



N,N-Dimethyl-p-toluidine, N,N-Dimethyl-p-toluidine, DMPT, Accelerator NL-65-100, N,N-DIMETHYL-P-TOLUIDINE 99%, N,N-DIMETHYL-P-TOLUIDINE 99%, DMPT, AcryliCon Low Temp Additive, Accelerator 101, Accelerator 101, N,N-DIMETHYL-P-TOLUIDINE (DMPT), N,N-Dimethyl-p-toluidine, 4-Dimethylaminotoluene, N,N,4-TRIMETHYLBENZENAMINE, N,N-DIMETHYL-4-METHYLANILINE, N,N-DIMETHYL-4-TOLUIDINE, N,N-DIMETHYL-PARA-TChemicalbookOLUIDINE, N,N-DIMETHYL-P-TOLUIDINE, Benzeneamine,N,N,4-trimethyl-, dimethyl-4-toluidine, Dimethyl-p-toluidine, N,N,4-Trimethylaniline;4,N,N-TrimethyL, N,N,4-trimethyl-, dimethyltoluidine, DIMETHYLTOLYLAMINE, Dimetil-p-toluidina, p-Toluidine, N,N-dimethyl-, p-Methyl-N,N-dimethylaniline, p,N,N-trimethylaniline, Dimethyl-p-toluidine, N,N-Dimethyl-p-toluidine, N,N-Dimethyl-p-tolylamine, N,N-Dimethyl-4-methylaniline, N,N,4-Trimethylbenzenamine, N,N-Dimethyl-4-toluidine, N,N,4-Trimethylaniline, Dimetil-p-toluidina, Benzeneamine,N,N,4-trimethyl-, 1-(Dimethylamino)-4-methylbenzene, NSC 1785, p-(Dimethylamino)toluene, Benzenamine, N,N,4-trimethyl-p-Toluidine, N,N-dimethyl-, N,N,4-Trimethylbenzenamine, N,N-Dimethyl-p-toluidine, p-Methyl-N,N-dimethylaniline,
Dimethyl-p-toluidine, N,N-Dimethyl-p-tolylamine, N,N-Dimethyl-4-methylaniline, p,N,N-Trimethylaniline, N,N,4-Trimethylaniline, p-(Dimethylamino)toluene, N,N-Dimethyl-p-methylphenylamine, N,N-Dimethyl-1,4-toluidine, N,N-Dimethyl-p-toluidene, 1-(Dimethylamino)-4-methylbenzene, NSC 1785, NL 65-100, 4-Dimethylamino-1-methylbenzene, N,N-Dimethyl-p-methylaniline, 4-(Dimethylamino)toluene, FirstCure DMPT, AC 103 (amine), AC 103, Benzenamine, N,N,4-trimethyl-, 4-Dimethylaminotoluene, Dimethyl-p-toluidine, DMPT, p-Toluidine, N,N-dimethyl- N,N,4-Trimethylaniline, p,N,N-Trimethylaniline, Benzenamine, N,N,4-trimethyl-, N,N-Dimethyl-p-Tolylamine, N,N-dimethyl-p-toluidine, Dimethyl-4-toluidine, N,N-Dimethyl-4-methylaniline, Dimethyl-p-toluidine, dimethyl-4-toluidine, N,N-Dimethyl-p-toluidine, N,N-DIMETHYL-4-TOLUIDINE, N,N-DIMETHYL-P-TOLUIDINE, N,N,4-TRIMETHYLBENZENAMINE, N,N-DIMETHYL-PARA-TOLUIDINE, N,N-DIMETHYL-4-METHYLANILINE, Benzeneamine,N,N,4-trimethyl-, N,N-Accelerator NL-65-100, 99-97-8, N,N,4-TRIMETHYLANILINE, Accelerator NL-65-100, Benzenamine, N,N,4-trimethyl-, Dimethyl-4-toluidine, N,N-Dimethyl-4-methylaniline, N,N,4-Trimethylbenzenamine, p-Methyl-N,N-dimethylaniline, p-(Dimethylamino)toluene, N,N-Dimethyl-p-tolylamine, 4-Dimethylaminotoluene, N,N-Dimethyl-para-toluidine, p-Toluidine, N,N-dimethyl-, NSC 1785, p,N,N-Trimethylaniline, Dimetil-p-toluidina, N,N-Dimethyl-4-toluidine, 1-(Dimethylamino)-4-methylbenzene, 4,N,N-Trimethylaniline, S8XC5939VU, DTXSID0021832, NSC-1785, NL 65-100, DTXCID401832, p-N,N-Trimethylaniline, CAS-99-97-8, CCRIS 1001, EINECS 202-805-4, UNII-S8XC5939VU, Benzeneamine,N,N,4-trimethyl-, Dimethyltolylamine, HSDB 8202, MFCD00008316, N,4-Trimethylaniline, dimethyl-(p-tolyl)-amine, EC 202-805-4, Benzenamine,N,4-trimethyl-, SCHEMBL28378, MLS001050174, 4-dimethylamino-1-methylbenzene, 4,N,N-Trimethylaniline, 99%, CHEMBL1462714, DIMETHYLTOLYLAMINE [INCI], N,N-Dimethyl-p-methylphenylamine, NSC1785, Tox21_201370, Tox21_300062, AC-368, AKOS015915159, N,N-ACCELERATOR NL-65-100 [IARC], NCGC00091397-01, NCGC00091397-02, NCGC00091397-03, NCGC00254201-01, NCGC00258922-01, SMR001216586, D0807, FT-0629511, FT-0636092, FT-0656134, E75885, EN300-7266829, 4,N,N-Trimethylaniline, purum, >=98.0% (GC), Q2051705, W-100002, Z1002998236, N,N-DIBENZYL-1,4,10,13-TETRAOXA-7,16-DIAZACYCLOOCTADECANE, N,N-Accelerator NL-65-100, 4-Dimethylaminotoluene, 4-Dimethylaminotoluene, N,N-dimethyl-4-methylaniline, p,N,Ntrimethylaniline, N,N,4-trimethylbenzenamine, N,N,4-Trimethylaniline, Accelerator NL-65-100, dimethyltoluidine, n,n-dimethyl-p-toluidin, N,N-DIMETHYL-4-TOLUIDINE, N,N-Dimethyl-p-tolylamine, N,N-DIMETHYL-4-METHYLANILINE, 4,N,N-TrimethyL, N,N,4-trimethyl-, DIMETHYLTOLYLAMINE, N,N,4-Trimethylaniline, 4-Dimethylaminotoluene, n,n-Accelerator NL-65-100, Accelerator NL-65-100, benzenamine, n,n,4-trimethyl, n,n-dimethyl-4-methylaniline, n,n-dimethyl-para-toluidine, 4,n,n-trimethylaniline, dimethyl-4-toluidine, p-dimethylamino toluene, n,n-dimethyl-p-tolylamine, n,n,4-trimethylbenzenamine, 4-Dimethylaminotoluene, Dimethyltolylamine, 4-Dimethylaminotoluene, N,N, 4-trimethylaniline, N,N,4-TRIMETHYLBENZENAMINE, N,N-DIMETHYL-4-METHYLANILINE, N,N-DIMETHYL-4-TOLUIDINE, N,N-DIMETHYL-PARA-TOLUIDINE, Benzenamine, N,N,4-trimethyl-, Dimethyl-4-toluidine, N,N,4-Trimethylaniline, N,N-Dimethyl-4-methylaniline, N,N-Accelerator NL-65-100, N,N-Dimethyl-p-tolylamine, p,N,N-Trimethylaniline, p-(Dimethylamino)toluene, p-Methyl-N,N-dimethylaniline, p-Toluidine, N,N-dimethyl-,



Accelerator NL-65-100 is used in pultrusion, resin transfer molding, filament winding, hand lay-up and spray-up applications.
The radical formation, which is necessary to start the polymerization reaction, is at ambient temperatures with most generally applied organic peroxides too slow.


Accelerator NL-65-100 form a group of substances in the chemical and aromatic compounds with a dimethylamino group [-N (CH3)2] and a methyl group (CH3) as a substituent on the benzene ring.
Accelerator NL-65-100 is colorless or lightyellow liquid, with the rotten egg smell.


The shelf life of Accelerator NL-65-100 is 9 months.
Accelerator NL-65-100 is listed in TSCA.
Accelerator NL-65-100 is a high-reactive amine accelerator used for curing unsaturated polyesters at ambient temperatures.


Accelerator NL-65-100 otherwise known as p,N,N-Trimethylaniline is an aromatic compound that is a member of the aniline family.
Accelerator NL-65-100 is supplied by Actylis in the form of a clear yellow liquid that is immiscible in water that has an aromatic odour.
Accelerator NL-65-100 is a clear colorless liquid with an aromatic odor. Density 0.937 g / cm3 and insoluble in water.


Accelerator NL-65-100 exists in clear colorless liquid with an aromatic odor.
Density of Accelerator NL-65-100 is 0.937 g / cm3 (Lancaster) and is insoluble in water.
Accelerator NL-65-100 is colorless or lightyellow liquid, with the rotten egg smell.


Accelerator NL-65-100 is insoluble in water, soluble in some organic solvents, will decomposition when exposure under the sun.
Accelerator NL-65-100appears as a clear colorless liquid with an aromatic odor.
Density of Accelerator NL-65-100 is 0.937 g / cm3 (Lancaster) and insoluble in water.


The curing of unsaturated polyester resins at ambient temperatures can in general not be performed by an organic peroxide alone.
The radical formation, which is necessary to start the polymerisation reaction, is at ambient temperatures with most generally applied organic peroxides too slow.


Accelerator NL-65-100 hence floats on water.
Accelerator NL-65-100 is a light yellow liquid
Accelerator NL-65-100 is miscible with alcohol, ether and chloroform.


Accelerator NL-65-100 is immiscible with water.
Accelerator NL-65-100 is incompatible with strong oxidizing agents.
Store Accelerator NL-65-100 in a cool place.


Accelerator NL-65-100 is a high-reactive amine accelerator used for curing unsaturated polyesters at ambient temperatures.
Accelerator NL-65-100 is a versatile organic compound extensively utilized in scientific research.
Accelerator NL-65-100's applications span across the synthesis of numerous compounds, including,agrochemicals, pesticides, amino acids, peptides, and nucleotides.


Accelerator NL-65-100 is a colorless or light yellow oily liquid with rotten egg smell, melting point 130.31℃, boiling point 211.5-212.5℃, weight 0.9287~0.9366g/mL at normal Chemicalbook temperature, refractive index 1.5360~1.5470, insoluble in water, soluble in some organic solvents, decomposing when exposed to light.


Accelerator NL-65-100 is miscible with alcohol, ether and chloroform.
Accelerator NL-65-100 is immiscible with water.
Accelerator NL-65-100 is incompatible with strong oxidizing agents.


Store Accelerator NL-65-100 in a cool place.
Accelerator NL-65-100 is a high-reactive amine accelerator used for curing unsaturated polyesters at ambient temperatures.
Accelerator NL-65-100 is an organic compound that is commonly used in organic synthesis and as a reagent in laboratory experiments.


Accelerator NL-65-100 is a colorless, crystalline solid that is soluble in most organic solvents.
Accelerator NL-65-100 appears as a clear colorless liquid with an aromatic odor.
Accelerator NL-65-100 is soluble in some organic solvents and is decomposed by light as an effective photoinitiator for acrylonitrile (AN) polymerization.
Accelerator NL-65-100 can also be used to make self-coagulation tooth tray water.



USES and APPLICATIONS of ACCELERATOR NL-65-100:
Accelerator NL-65-100 is used engineered Stone, Pultrusion, Resin Transfer Molding, Filament winding, Chemical anchors & mine bolts, Hand lay-up & spray-up
Accelerator NL-65-100 is used curing accelerator for unsaturated polyester resins.
To speed up the radical formation in a controllable way, organic peroxides must therefore be used in combination with a so-called accelerator.


To speed up the radical formation in a controllable way, organic
peroxides must therefore be used in combination with a so-called accelerator.
Accelerator NL-65-100 is an amine accelerator for curing UP resins.


Accelerator NL-65-100 is used for synthesis is a high-quality compound that offers exceptional performance in diverse applications.
Its unique composition and excellent results make Accelerator NL-65-100 an ideal choice for scientific research and industrial processes.
Accelerator NL-65-100 is used for self-condensation.


Pharmaceutical Research uses of Accelerator NL-65-100: Accelerator NL-65-100 plays a crucial role in pharmaceutical research, serving as a catalyst or intermediate in the synthesis of active pharmaceutical ingredients (APIs) and other drug-related compounds.
Accelerator NL-65-100 is used for synthesis and is a high-quality, effective compound used in various applications.


Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.
Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.


With its unique composition and excellent performance, Accelerator NL-65-100 is ideal for scientific research and industrial purposes.
Accelerator NL-65-100 is used as a polymerization catalyst for Intermediate for primarily polyesters and acrylate and epoxy resins.
Accelerator NL-65-100 can be used as a hardner for dental cements and for adhesives.


Accelerator NL-65-100 is used as an intermediate for photographic chemicals, colorants and pharmaceuticals.
Accelerator NL-65-100 is an effective photoinitiator for the polymerization of acrylonitrile (AN).
Accelerator NL-65-100 is used for synthesis has found extensive use in various applications.


Accelerator NL-65-100 is used to make acrylic resins and denture materials.
Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.


Accelerator NL-65-100 is used as a chemical bond for polyesters, acrylate, and epoxy resins.
Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 can be found in dental products, photographic materials, colorants, and pharmaceuticals.


Accelerator NL-65-100 reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.
Accelerator NL-65-100 is used as an effective photoinitiator for polymerization of acrylonitrile (AN)


Accelerator NL-65-100 is used a tertiary amine, which can be coupled with phenylacetylene and benzamide in the presence of Di tert butyl peroxides by iron catalyzed oxidation C-C, respectively to form n, 4-dimethyl-n - (3-phenylpropyl-2-alkynyl) benzoylamine and N - ((methyl (p-tolyl)amino) methyl) benzoylamine.


Accelerator NL-65-100 reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Further, Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.
Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.


Accelerator NL-65-100 is used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.


Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.
Accelerator NL-65-100 is used as an effective photo initiator for the polymerization of acrylonitrile (AN), its polymerization rate is proportional to the 1.62 power of AN concentration and the 0.62 power of DMT concentration.


Accelerator NL-65-100 is usually used as an accelerator, and can also be used as an additive for the synthesis of unsaturated polyesters and adhesives.
Accelerator NL-65-100 is used as a polymerization catalyst and intermediate in preparing polyesters and acrylate and epoxy resins.
Accelerator NL-65-100 can be used as a hardner for dental cements and for adhesives.


Accelerator NL-65-100 is used as an intermediate for photographic chemicals, colorants and pharmaceuticals.
Accelerator NL-65-100 is an amine accelerator for the polymerization of e.g. dental methacrylic restorative materials
Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.


Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals. It reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.


Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.


Accelerator NL-65-100 reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Further, Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.
Accelerator NL-65-100 is soluble in some organic solvents, decomposed by light, as an effective photoinitiator for acrylonitrile (AN) polymerization; it can also be used to make self-consolidating dental tray water.


Further, Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.
Accelerator NL-65-100 is often used as a catalyst for the polymerization of polyesters and epoxy resins.
Accelerator NL-65-100 has also been used as a chemical hardener in dentistry adhesives.


Accelerator NL-65-100 has also been used as a chemical intermediate in the synthesis of various pharmaceutical products, colorants and artificial fingernail preparations as well as a raw material in the synthesis of industrial adhesives.
Accelerator NL-65-100 is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.


Accelerator NL-65-100 is also used as a hardener for dental cements and in adhesives.
Accelerator NL-65-100 serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.


Accelerator NL-65-100 reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Further, Accelerator NL-65-100 is used to accelerate polymerization of ethyl methacrylate.


Aromatic tertiary amines, especially Accelerator NL-65-100, are effective photoinitiators for the polymerization of acrylonitrile (AN).
Accelerator NL-65-100 is usually considered as a retarder for alkene polymerization rather than a photoinitiator for acrylonitrile (AN) polymerization.
As an effective photoinitiator for acrylonitrile (AN) polymerization, its polymerization rate is proportional to 1.62 times the AN concentration and 0.62 times the Accelerator NL-65-100 concentration.


Accelerator NL-65-100 is commonly used as an accelerator, in addition to the synthesis of unsaturated polyesters and as an additive for adhesives, etc.
Accelerator NL-65-100 was synthesized by using dimethyl sulfate as a methylating agent at low temperature and atmospheric pressure. It is used to make self-consolidating dental tray water.


A tertiary amine that can be iron-catalyzed oxidative C-C coupled with phenylethynyl and benzamide in the presence of di-tert-butyl peroxide to form N,4-dimethyl-N-(3-phenyl prop-2-only)benzylamine, and N-((methyl(p-tolyl)amino)methyl)benzamide, respectively.
Accelerator NL-65-100 finds utility in the creation of polymers, dyes, and catalysts.


As a colorless, crystalline solid, Accelerator NL-65-100 easily dissolves in most organic solvents.
As a nucleophilic reagent capable of reacting with both electrophiles like carbonyl compounds and halides, as well as nucleophiles such as amines and alcohols.


With its wide range of applications, Accelerator NL-65-100 serves as a crucial reagent for the synthesis of various compounds in laboratory settings.
Accelerator NL-65-100 is used to make self-curing dental tray water; glue accelerator, marble glue; production of anchoring agent. Used in dyes, medicine and other organic synthesis.


Accelerator NL-65-100 is also used in the production of pharmaceuticals, agrochemicals, and pesticides.
Accelerator NL-65-100 has a wide range of applications in the laboratory and is an important reagent for the synthesis of a variety of compounds.
Accelerator NL-65-100 is used for the preparation of self-curing dental water


As an effective photoinitiator for acrylonitrile (AN) polymerization, its polymerization speed is proportional to the 1.62 power of AN concentration and the 0.62 power of Accelerator NL-65-100 concentration.
Accelerator NL-65-100 is usually used as an accelerator, and can also be used as an additive for the synthesis of unsaturated polyester, adhesive, etc.
Accelerator NL-65-100 is used to make self-setting tooth tray water.


-Chemical Synthesis uses of Accelerator NL-65-100:
Accelerator NL-65-100 serves as a valuable reagent in chemical synthesis, especially in the production of dyes, polymers, and specialty chemicals.
Accelerator NL-65-100's versatile nature allows for numerous transformations and reactions.


-Electrochemical Processes uses of Accelerator NL-65-100:
Accelerator NL-65-100 finds application in electrochemical processes, such as the synthesis of conductive polymers and batteries.
Accelerator NL-65-100's unique properties contribute to enhanced performance in these applications.


-Material Science uses of Accelerator NL-65-100:
Accelerator NL-65-100 is utilized in various material science research, including the production of coatings, adhesives, and sealants.
Accelerator NL-65-100 contributes to the development of advanced materials with improved properties.



FUNCTIONS OF ACCELERATOR NL-65-100:
*Accelerator



PHYSICAL AND CHEMICAL PROPERTIES OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 is a colorless or light yellow oily liquid with rotten egg flavor, melting point 130.31 ℃, boiling point 211.5-212.5 ℃, severe 0.9287~0.9366 g/mL at normal temperature, refractive index 1.5360~1.5470, insoluble in water, soluble in some organic solvents, and decomposed in light.



OVERVIEW OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 is a crucial compound used in synthesis processes.
With its highly specific composition and exceptional purity, Accelerator NL-65-100 offers reliable and precise results that meet the demands of various scientific and industrial applications.
Accelerator NL-65-100 has a molecular formula of 4-(CH3)C6H4N(CH3)2 and a CAS number of 99-97-8, allowing for easy identification and traceability.



FEATURES AND BENEFITS OF ACCELERATOR NL-65-100:
*High Quality:
Accelerator NL-65-100 for synthesis is manufactured to meet the highest quality standards.
Each batch undergoes rigorous testing to ensure purity, consistency, and reliability.

*Effective Performance:
With its unique composition, Accelerator NL-65-100 offers exceptional performance in various synthesis processes.
Accelerator NL-65-100's effectiveness has been demonstrated through extensive research and application.

*Wide Range of Applications:
Accelerator NL-65-100 is versatile and finds application in several industries such as pharmaceutical, chemical, and material science.
Its properties make Accelerator NL-65-100 suitable for diverse synthesis processes.

*Easy to Use:
Accelerator NL-65-100 for synthesis is formulated to be user-friendly, allowing for convenient handling and integration into existing protocols.

*Reliable Results:
The consistent quality of Accelerator NL-65-100 ensures reliable and reproducible results, crucial for scientific research and industrial processes.



DETAILS OF ACCELERATOR NL-65-100:
N,N-Accelerator NL-65-100, also known as 4-Dimethylaminotoluene, is composed of a linear formula of 4-(CH3)C6H4N(CH3)2. This formula represents the arrangement of atoms in the compound, providing essential information about its structure and properties.



AIR AND WATER REACTIONS OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 tends to darken upon exposure to air.
Accelerator NL-65-100 is insoluble in water.



POLYMERIZATION REACTION OF ACCELERATOR NL-65-100:
Aromatic tertiary amines, especially Accelerator NL-65-100, are effective photoinitiators for acrylonitrile (AN) polymerization.
The influence of the medium on the polymerization speed is large in polarity, and the polymerization speed is fast.
Oxygen has obvious influence on the polymerization.
With the increase of oxygen content, the polymerization induction period increases and the speed decreases.
Accelerator NL-65-100 is generally considered as a retarder for alkene polymerization, rather than a photopolymerization initiator for acrylonitrile (AN).



AGGREGATION FEATURES OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 cannot initiate acrylonitrile (AN) polymerization in the dark, but the polymerization is extremely fast under light.
Accelerator NL-65-100 initiated acrylonitrile (AN) photopolymerization is carried out according to a free radical mechanism.
When a trace amount of free radical capture agent is added, the polymerization is completely stopped.



REACTIVITY PROFILE OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 neutralizes acids in exothermic reactions to form salts plus water.
Accelerator NL-65-100 may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.
Accelerator NL-65-100 may generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.



SYNTHESIS OF ACCELERATOR NL-65-100:
Accelerator NL-65-100 was prepared by reacting p-toluidine with methanol and POCl3 in autoclave heated up to 280° C for 3h.



PURIFICATION METHODS OF ACCELERATOR NL-65-100:
Reflux for 3hours with 2 molar equivalents of Ac2O, then fractionally distil Accelerator NL-65-100 under reduced pressure.
Alternatively, dry Accelerator NL-65-100 over BaO, distil and store it over KOH.
The picrate has m 128o (from EtOH).



SYNTHESIS METHOD OF ACCELERATOR NL-65-100:
Using dimethyl sulfate as a methylating agent, Accelerator NL-65-100 was synthesized at low temperature and normal pressure.



PHYSICAL and CHEMICAL PROPERTIES of ACCELERATOR NL-65-100:
Appearance: Clear light yellow to light
Assay: ≥ 98.5 %
Viscosity, 20°C: 2 mPa.s
Boiling point: 211 °C
Density: 20 °C 0.935 g/cm³
Melting point: -25 °C
CAS number: 99-97-8
Physical form: Liquid
Chemical name: N,N-Dimethyl p-toluidine
Physical State :Liquid
Solubility :Soluble in water (0.65 mg/ml at 37° C), alcohol, ether, and chloroform.
Storage :Store at room temperature
Melting Point :-25° C
Boiling Point :211° C (lit.)
Density :0.94 g/mL at 25° C (lit.)
Refractive Index :n20D 1.55 (lit.)

pK Values :
pKa: 5.63 at 25 C
CAS No.: 99-97-8
Molecular Formula: C9H13N
InChIKeys: InChIKey=GYVGXEWAOAAJEU-UHFFFAOYSA-N
Molecular Weight: 135.20600
Exact Mass: 135.21
EC Number: 202-805-4
PSA: 3.24000
XLogP3: 2.06100
Density: 0.9 g/cm3
Melting Point: 113-115 °C @ Solvent: Acetic acid
Boiling Point: 215 °C
Flash Point: 83ºC
Refractive Index: 1.545-1.547
Water Solubility: Solubility in water: none
Storage Conditions: Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Vapor Pressure: 0.1 hPa (20 °C)

Vapor Density: >1 (vs air)
Explosive limit: Upper explosion limit: 7 %(V); Lower explosion limit: 1.2 %(V)
Odor: Aromatic
Density: 0.936 (204 c)
Insolubility: in water
Refractive Index: 1.546 (20 c)
Molecular weight: 135.23
Flash Point: 7 c
Solubility: oxygenated solvs.
Boiling Point: 210-211 c (760 mm)
CAS: 99-97-8
EINECS: 202-805-4
InChI: InChI=1/C9H13N/c1-8-4-6-9(7-5-8)10(2)3/h4-7H,1-3H3
Molecular Formula: C9H13N
Molar Mass: 135.21
Density: 0.937
Melting Point: -25°C

Boling Point: 211℃
Flash Point: 83℃
Water Solubility: Miscible with alcohol, ether and chloroform.
Immiscible with water.
Vapor Presure: 0.1 hPa (20 °C)
Refractive Index: 1.545
vapor density: >1 (vs air)
Vapor pressure: 0.1 hPa (20 °C)
refractive index: n20/D 1.546(lit.)
flash point: 182 °F
storage conditions: Store below +30°C.
solubility: 0.65g/l
acidity coefficient (pKa): pK1:7.24(+1) (25°C)
morphology: Liquid
color: Clear yellow
explosion limit value (explosive limit) 7%
water solubility: Miscible with alcohol, ether and chloroform.
Immiscible with water.
BRN: 774409

stability: Stable.
Incompatible with strong oxidizing agents.
InChIKey: GYVGXEWAOAAJEU-UHFFFAOYSA-N
Color: Yellow
Density: 0.9300g/mL
Boiling Point: 211.0°C
Flash Point: 83°C
Infrared Spectrum: Authentic
Assay Percent Range: 98.5% min. (GC)
Linear Formula: CH3C6H4N(CH3)2
Refractive Index: 1.5450 to 1.5470
Beilstein: 12, 902
Specific Gravity: 0.93
Solubility Information:
Solubility in water: immiscible
Formula Weight: 135.21
Percent Purity: 99%
Physical Form: Liquid
Chemical Name or Material: N, N-Dimethyl-p-toluidine, 99%

Molecular Weight: 135.21 g/mol
XLogP3: 2.8
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 1
Exact Mass: 135.104799419 g/mol
Monoisotopic Mass: 135.104799419 g/mol
Topological Polar Surface Area: 3.2Ų
Heavy Atom Count: 10
Formal Charge: 0
Complexity: 90.9
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS Number: 99-97-8
Molecular Weight: 135.21
MDL number: MFCD00008316
EC Index Number: 202-805-4
Molecular Formula: C9H13N
CH3C6H4N(CH3)2
CBNumber:CB4196682
Molecular Formula:C9H13N
Molecular Weight:135.21
MDL Number:MFCD00008316
MOL File:99-97-8.mol
Melting point: -25°C
Boiling point: 211 °C(lit.)

Density: 0.937 g/mL at 25 °C(lit.)
vapor density: >1 (vs air)
vapor pressure: 0.1 hPa (20 °C)
refractive index: n20/D 1.546(lit.)
Flash point: 182 °F
storage temp.: Store below +30°C.
solubility: 0.65g/l
form: Liquid
pka: pK1:7.24(+1) (25°C)
color: Clear yellow
explosive limit: 7%
Water Solubility: Miscible with alcohol, ether and chloroform.
Immiscible with water.
BRN: 774409

Dielectric constant: 3.3(20℃)
Stability: Stable.
Incompatible with strong oxidizing agents.
InChIKey: GYVGXEWAOAAJEU-UHFFFAOYSA-N
LogP: 1.729-2.81 at 35℃
CAS DataBase Reference: 99-97-8(CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: S8XC5939VU
Proposition 65 List: N,N-Accelerator NL-65-100
IARC: 2B (Vol. 115) 2018
EPA Substance Registry System: N,N,4-Trimethylaniline (99-97-8)
Physical state: oily
Color: beige
Odor: unpleasant

Melting point/freezing point:
Melting point: -15 °C - (ECHA)
Initial boiling point and boiling range: 90 - 92 °C at 13 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 7 %(V)
Lower explosion limit: 1,2 %(V)
Flash point: 76 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 7,44 at 25 °C
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 14,4 mPa.s at 35 °C

Water solubility: 0,65 g/l at 37 °C
Partition coefficient: n-octanol/water:
log Pow: 1,73 at 35 °C
Vapor pressure: 0,099 hPa at 20 °C
Density: 0,936 g/cm3
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information:
Relative vapor density: 5,42
CAS number: 99-97-8
EC index number: 612-056-00-9

EC number: 202-805-4
Hill Formula: C₉H₁₃N
Chemical formula: 4-(CH₃)C₆H₄N(CH₃)₂
Molar Mass: 135.21 g/mol
HS Code: 2921 43 00
Boiling point: 215 °C (1013 hPa)
Density: 0.88 g/cm3 (35 °C)
Flash point: 76 °C
Ignition temperature: 425 °C
Melting Point: -15 °C
pH value: 7.44 (H₂O, 25 °C)
Vapor pressure: 0.099 hPa (20 °C)
Solubility: 0.65 g/l
CAS: 99-97-8

Molecular Formula: C9H13N
Molecular Weight (g/mol): 135.21
MDL Number: MFCD00008316
InChI Key: GYVGXEWAOAAJEU-UHFFFAOYSA-N
Melting Point: -25°C
Density: 0.937
Boiling Point: 210°C to 211°C
Flash Point: 83°C (181°F)
Refractive Index: 1.546
UN Number: UN1708
Beilstein: 774409

Solubility Information: Miscible with alcohol,ether and chloroform.
Immiscible with water.
Formula Weight: 135.21
Chemical Name or Material: N,N-Accelerator NL-65-100
Molecular Formula: C9H13N
Molecular Weight: 135.21
Description: A light yellow coloured oily liquid.
Assay: 99.0% (min).
Specific Gravity: 0.936 to 0.940 at 200/200C.
Other Organic Impurities: 0.5% (max)
Other Toluidines: 1.0% (max)
Moisture content by KF: 0.1% (max)



FIRST AID MEASURES of ACCELERATOR NL-65-100:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of ACCELERATOR NL-65-100:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.



FIRE FIGHTING MEASURES of ACCELERATOR NL-65-100:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ACCELERATOR NL-65-100:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ACCELERATOR NL-65-100:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ACCELERATOR NL-65-100:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
no information available



ACCELERATOR TMTD
Accelerator TMTD is a very active, sulfur-bearing, non-discoloring rubber accelerator.
Accelerator TMTD is also available in several color-coded polymer-bound masterbatch forms.
Accelerator TMTD acts as a primary accelerator for curing systems requiring very low or no sulfur.

CAS: 137-26-8
MF: C6H12N2S4
MW: 240.43
EINECS: 205-286-2

Synonyms
1,1’-dithiobis(n,n-dimethylthio-formamid;1,1’-dithiobis(n,n-dimethylthioformamide);Aapirol;Accel TMT;Accelerator T;Accelerator Thiuram;acceleratort;acceleratorthiuram;thiram;Tetramethylthiuram disulfide;137-26-8;Thiuram;Rezifilm;TMTD;Pomarsol;Thirame;Arasan;Fernasan;Nobecutan;Thioscabin;Thirasan;Aapirol
;Tersan;Tetrathiuram disulfide;Tetramethylthiuram;Falitiram;Formalsol;Hexathir;Kregasan;Mercuram;Normersan;Sadoplon;Spotrete;Tetrasipton;Thillate;Thiramad;Aatiram;Atiram;Fermide;Fernide;Hermal;Pomasol;Puralin;Thiosan;Thiotox;Thiulin;Thiulix;Heryl;Pomarsol forte;Methyl tuads;Accelerator T;Methyl Thiram;Fernasan A;Tetramethylthiuram disulphide;Nocceler TT;Arasan-M;Bis(dimethylthiocarbamoyl) disulfide;Thiram B;Arasan-SF;Cyuram DS;Ekagom TB;Hermat TMT;Tetramethylenethiuram disulfide;Accel TMT;Accelerator thiuram;Aceto TETD;Radothiram;Royal TMTD;Tetramethyl-thiram disulfid;Fernacol;Sadoplon 75;Tetramethylthiuram bisulfide;Tetrapom;Thioknock;Thirampa;Thiramum;Anles;Arasan-SF-X;Aules;Thimer;Panoram 75;Tetramethylthiouram disulfide;Tetramethylthiurane disulfide;Arasan 70;Arasan 75;Tersan 75;Thiram 75;Thiram 80;Spotrete-F;TMTDS;Arasan 70-S Red;Tetramethylthioperoxydicarbonic diamide;Methylthiuram disulfide;N,N-Tetramethylthiuram disulfide;Metiurac;Micropearls;Nomersan;Thianosan;Cunitex;Delsan;Thimar;Teramethylthiuram disulfide;Tersantetramethyldiurane sulfide;Pol-Thiuram;Arasan 42-S;Tetramethylthiurum disulfide;Disulfure de tetramethylthiourame;Tetrathiuram disulphide;Sranan-sf-X;Hy-Vic;SQ 1489;Chipco thiram 75;Bis(dimethyl-thiocarbamoyl)-disulfid;Orac TMTD;Tetramethylthioramdisulfide;Tetramethyldiurane sulphite;Thiotox (fungicide);Disulfide, bis(dimethylthiocarbamoyl);Bis((dimethylamino)carbonothioyl) disulfide;Fermide 850;Tetramethyl thiuramdisulfide;Tetramethylthiocarbamoyldisulphide;Thiuramyl;Thylate;Methyl thiuramdisulfide;Bis(dimethylthiocarbamyl) disulfide;Tetramethyl thiurane disulfide;Bis(dimethyl thiocarbamoyl)disulfide;Thirame [INN-French];Thiramum [INN-Latin];Thiuram D;Disolfuro di tetrametiltiourame;Tetramethyl thiurane disulphide;Tetramethylenethiuram disulphide;N,N'-(Dithiodicarbonothioyl)bis(N-methylmethanamine);RCRA waste number U244;Flo Pro T Seed Protectant;Tetramethylthiuram bisulphide

An organic disulfide that results from the formal oxidative dimerisation of N,N-dimethyldithiocarbamic acid.
Accelerator TMTD is widely used as a fungicidal seed treatment.
A liquid solution of a white crystalline solid.
Primary hazard is to the environment.
Immediate steps should be taken to limit spread to the environment.
Easily penetrates the soil to contaminates groundwater and waterways.
Accelerator TMTD is a rubber chemieal, an accelerator of vulcanization.
Accelerator TMTD represents the most commonly positive allergen contained in the "thiuram mix".
The most frequent occupational categories are the metal industry, homemakers, health services and laboratories, building industries, and shoemakers.

Accelerator TMTD Chemical Properties
Melting point: 156-158 °C(lit.)
Boiling point: 129 °C (20 mmHg)
Density: 1.43
Vapor pressure: 8 x 10-6 mmHg at 20 °C (NIOSH, 1997)
Refractive index: 1.5500 (estimate)
Fp: 89°C
Storage temp.: under inert gas (argon)
Solubility: 0.0184g/l
Form: solid
pka: 0.87±0.50(Predicted)
Water Solubility: 16.5 mg/L (20 ºC)
Merck: 14,9371
BRN: 1725821
Exposure limits: NIOSH REL: TWA 0.5 mg/m3, IDLH 100 mg/m3; OSHA PEL: 0.5 mg/m3; ACGIH TLV: TWA 5 mg/m3.
InChIKey: KUAZQDVKQLNFPE-UHFFFAOYSA-N
LogP: 1.730
CAS DataBase Reference: 137-26-8(CAS DataBase Reference)
NIST Chemistry Reference: Accelerator TMTD (137-26-8)
IARC: 3 (Vol. Sup 7, 53) 1991
EPA Substance Registry System: Accelerator TMTD (137-26-8)

Accelerator TMTD requires the addition of zinc oxide and fatty acid for effective use in most compounding applications.
Accelerator TMTD is used to activate thiazole or sulfenamide cure systems to improve scorch resistance.
Accelerator TMTD exhibits excellent dispersibility and can be encapsulated with chemical dispersion.
Accelerator TMTD is also available in pellets and micro granules form to reduce dusting.
Accelerator TMTD is easy to handle polymer-bound dispersion providing better uniformity of mix at low temperature, upgrade plant safety and quality.
Recommended for NR, SBR, NBR, EPDM, rubber elastomers and blends.
For most compounding applications, TMTD-MG requires the addition of zinc oxide and a fatty acid for effective use.
Sulfur is not required but is often used.
Accelerator TMTD is widely used as a primary accelerator for curing systems requiring very low or no sulfur.

Accelerator TMTD contains 13% available sulfur.
Accelerator TMTD is often used to activate thiazole or sulfenamide cure
systems.
Improved scorch resistance can be obtained in Accelerator TMTD stocks by the use of the thiazole or sulfenamide accelerators as primary accelerators.
TMTD-MG can be used as a cure modifier in carbon black loaded CR formulations to improve scorch properties. TMTD-MG is a white micro granule.
TMTD-MG offers the rubber chemist a handy, low dusting form of TMTD.
The novel micro-granular
consistency provides outstanding dispersion while limiting plant personnel to unnecessary hazardous exposure.
The MG particles are oil free and exhibit a very high chemical purity.
TMTD-MG is recommended for use in soft rubber compounds, where poor dispersion can not be tolerated.

Uses
1. Accelerator TMTD belongs to protective fungicides of broad spectrum, with a residual effect period of up to 7d or so.
Accelerator TMTD is mainly used for dealing with seeds and soil and preventing powdery mildew, smut and rice seedlings damping-off of cereal crops.
Accelerator TMTD can also be used for some fruit trees and vegetable diseases.
For example, dressing seed with 500g of 50% wettable powder can control rice blast, rice leaf spot, barley and wheat smut.

2. As pesticides, Accelerator TMTD is often referred to as thiram and is mainly used for the treatment of seeds and soil and the prevention and controlling of cereal powdery mildew, smut and vegetable diseases.
Accelerator TMTD, as the super accelerator of natural rubber, synthetic rubber and latex, is often referred to as accelerator TMTD and is the representative of thiuram vulcanization accelerator, accounting for 85% of the total amount of similar products.
Accelerator TMTD is also the super accelerator of natural rubber, diene synthetic rubber, Ⅱ, R and EPDM, with the highest utilization rate of all.
The vulcanization promoting force of Accelerator TMTD is very strong, but, without the presence of zinc oxide, it is not vulcanized at all.

3. Used for the manufacture of cables, wires, tires and other rubber products.
4. Used as the super accelerator of natural rubber, synthetic rubber and latex.
5. Used as the late effect promoter of natural rubber, butadiene rubber, styrene-butadiene rubber and polyisoprene rubber.
6. Used for the pest control of rice, wheat, tobacco, sugar beet, grapes and other crops, as well as for the seed dressing and soil treatment.
7. Tetramethylthiuram Disulfide is suitable for the manufacture of natural rubber, synthetic rubber and latex, and can also be used as curing agent.
Accelerator TMTD is the second accelerator of thiazole accelerators, which can be used with other accelerators as the continuous vulcanization accelerator.

8. In rubber industry, Tetramethylthiuram Disulfide can be used as the super-vulcanization accelerator, and aften used with thiazole accelerator.
Accelerator TMTD can also be used in combination with other accelerators as the continuous rubber accelerator.
For slowly decomposing out of free sulfur at more than 100 ℃, Accelerator TMTD can be used as curing agent too.
Accelerator TMTD's products have excellent resistance to aging and heat, so it is applicable to natural rubber, synthetic rubber and is mainly used in the manufacture of tires, tubes, shoes, cables and other industrial products.
In agriculture, Accelerator TMTD can be used as fungicide and insecticide, and it can also be used as lubricant additives.
9. Production methods from dimethylamine, carbon disulfide, ammonia condensation reaction was dimethyl dithiocarbamate, and then by the oxidation of hydrogen peroxide to the finished product.

Production Method
The preparation of sodium dimethyl dithiocarbamate(SDD): the reaction of dimethylamine hydrochloride and carbon disulfide in the presence of sodium hydroxide can generate sodium dimethylamino dithiocarbamate.
The reaction temperature is 50~55℃ and the pH value is 8~9.
The preparation of thiram: the reaction of SDD (or Diram) and hydrogen peroxide in the presence of sulfuric acid can produce thiram.
The reaction temperature is controlled at 10 ℃ below and the end pH value is 3 to 4.
Chlorine can also be used instead of hydrogen peroxide and sulfuric acid.
The reaction is performed in the sieve tray tower, from the bottom of which the diluted chlorine is introduced and from the top of which 5% sodium solution is sprayed, which is called chlorine-air oxidation method.
There are also other methods, such as sodium nitrite oxidation or electrolytic oxidation.

Carcinogenicity
Accelerator TMTD also was not carcinogenic in rats by gavage or in mice by single subcutaneous injection.
In skin painting studies in mice thiram had tumor-initiating and -promoting activity but was not a complete carcinogen.
Accelerator TMTD was genotoxic to insects, plants, fungi, and bacteria: it induced sister chromatid exchange and unscheduled DNA synthesis in cultured human cells.
Despite established genotoxicity in vitro, Accelerator TMTD showed no clastogenic and/or aneugenic activity in vivo after oral administration to mice at the maximum tolerated dose.

Contact Allergens
This rubber chemical, accelerator of vulcanization, represents the most commonly positive allergen contained in “thiuram mix.”
The most frequent occupational categories are the metal industry, homemakers, health services and laboratories, the building industry, and shoemakers.
Accelerator TMTD is also widely used as a fungicide, belonging to the dithiocarbamate group of carrots, bulbs, and woods, and as an insecticide.
Accelerator TMTD is the agricultural name for thiuram.
ACEMATT OK 412
AEROSIL(TM) 200; BAKER SILICA GEL; CAB-OSIL M-5; CAB-O-SIL(TM) M-5; COLLOIDAL SILICA; CRISTOBALITE; DAVISIL(TM); DRYING PEARLS ORANGE; IATROBEADS; LICHROSORB(R) 60; PHTHALOCYANINE IMMOBILIZED SILICA GEL; POTASSIUM HYDROXIDE-IMPREGNATED SILICA GEL; PRESEP(R) SILICA GEL TYPE 3L; QUARTZ; SAND; SILICA; SILICA GEL; SILICA GEL 100; SILICA GEL 12-28 MESH; SILICA GEL 30 CAS NO:112945-52-5
ACEMATT TS 100
ACEMATT TS 100 IUPAC Name dioxosilane ACEMATT TS 100 InChI InChI=1S/O2Si/c1-3-2 ACEMATT TS 100 InChI Key VYPSYNLAJGMNEJ-UHFFFAOYSA-N ACEMATT TS 100 Canonical SMILES O=[Si]=O ACEMATT TS 100 Molecular Formula (SiO2)n ACEMATT TS 100 CAS 7631-86-9 ACEMATT TS 100 Deprecated CAS 108727-71-5 ACEMATT TS 100 European Community (EC) Number 231-545-4 ACEMATT TS 100 ICSC Number 0248 ACEMATT TS 100 RTECS Number VV7325000 ACEMATT TS 100 DSSTox Substance ID DTXSID1029677 ACEMATT TS 100 Physical Description PelletsLargeCrystals, OtherSolid, Liquid ACEMATT TS 100 Color/Form Amorphous powder ACEMATT TS 100 Odor Odorless ACEMATT TS 100 Taste Tasteless ACEMATT TS 100 Boiling Point 4046 °F at 760 mm Hg ACEMATT TS 100 Melting Point 3110 °F ACEMATT TS 100 Solubility Insoluble ACEMATT TS 100 Density 2.2 ACEMATT TS 100 Vapor Pressure 0 mm Hg ACEMATT TS 100 Corrosivity Non-corrosive ACEMATT TS 100 Heat of Combustion /Non-combustible/ ACEMATT TS 100 Molecular Weight 60.084 g/mol ACEMATT TS 100 Hydrogen Bond Donor Count 0 ACEMATT TS 100 Hydrogen Bond Acceptor Count 2 ACEMATT TS 100 Rotatable Bond Count 0 ACEMATT TS 100 Exact Mass 59.966756 g/mol ACEMATT TS 100 Monoisotopic Mass 59.966756 g/mol ACEMATT TS 100 Topological Polar Surface Area 34.1 Ų ACEMATT TS 100 Heavy Atom Count 3 ACEMATT TS 100 Formal Charge 0 ACEMATT TS 100 Complexity 18.3 ACEMATT TS 100 Isotope Atom Count 0 ACEMATT TS 100 Defined Atom Stereocenter Count 0 ACEMATT TS 100 Undefined Atom Stereocenter Count 0 ACEMATT TS 100 Defined Bond Stereocenter Count 0 ACEMATT TS 100 Undefined Bond Stereocenter Count 0 ACEMATT TS 100 Covalently-Bonded Unit Count 1 ACEMATT TS 100 Compound Is Canonicalized Yes ACEMATT TS 100 is an untreated thermal silica characterized by very high matting efficiency combined with very high transparency. Thanks to the unique properties ACEMATT TS100 is particularly suitable for coating systems that are difficult to matte.ACEMATT TS 100 can be used in water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACEMATT TS 100 show outstanding resistance against household chemicals. ACEMATT TS 100 improves flow behavior and increases storage stability in powder coatings.ACEMATT TS 100 is an untreated thermal silica with outstanding properties. It provides very high efficiency and transparency. It can be used in a large variety of coatings.ACEMATT TS 100 is a high performance matting agent adding versatility to your nail polish formulations. Only low levels of addition give a matt or crackle finish. The product, which is a fumed silica is listed with the INCI name 'Silica'.ACEMATT TS 100 by Evonik acts as a matting agent for powder coatings, overprint lacquers and printing inks. Offers very good matting efficiency and transparency. Exhibits very good resistance to household chemicals. ACEMATT TS 100 provides improved flow behavior and storage stability.Properties and applications: ACEMATT TS 100/20 is an untreated thermal silica characterized by very high matting efficiency combined with high transparency. Thanks to the unique properties, ACEMATT TS 100/20 is particularly suitable for coating systems that are difficult to matt. Special application areas include: water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACEMATT TS 100/20 show outstanding resistance against household chemicals. The particle size distribution in ACEMATT TS 100/20 is slightly broader than in ACEMATT TS 100. ACEMATT TS 100/20 improves flow behavior and increases storage stability in powder coatings.Product information ACEMATT TS 100 Evonik Industries AG | Product information ACEMATT TS 100 | Mar 2012 Page 1/2Properties and test methods Unit Value Loss on drying2 h at 105°C following ISO 787­2%≤ 4Loss on ignition 1)2 h at 1000°C following ISO 3262­1%≤ 2.5pH value5 % in water Following ISO 787­9­6.5Particle size, d50Laser diffraction following ISO 13320­1μm9.5Specific surface area (N2) Multipoint following ISO 9277m2/g250SiO2 content 2)following ISO 3262­19%≥ 99Package size (net)kg101) based on dried substance 2) based on ignited substance *) The given data are typical values. Specifications on request.Characteristic physico­ chemical data*)ACEMATT TS 100CAS­No.112945­52­57631­86­9REACH (Europe)registered TSCA (USA)registered DSL (Canada)registered AICS (Australia)registered KECI (Korea)registered ENCS (Japan)registered PICCS (Philippines)registered IECS (China)registered NZIoC (New Zealand)registered Registrations ACEMATT Matting agents are high performance silica developed for a variety of applications in Paints & Coatings. Properties and applications ACEMATT TS 100 is an untreated thermal silica characterised by very high matting efficiency combined with very high transparency. Thanks to the unique properties, ACEMATT TS 100 is particularly suitable for coating systems that are difficult to matt. It can be used in water­based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACMATT® TS 100 show outstanding resistance against household chemicals.Due to the high purity and extremely low electrical conductivity, ACEMATT TS 100 is outstanding for applications in sensitive coating systems such as solder resist.ACEMATT TS 100 improves flow behavior and increases storage stability in powder coatings.Safety and handlingInformation concerning the safety of this product is listed in the corresponding Material Safety Data Sheet, which will be sent with the first delivery or upon updating. Such information is also available from Evonik Industries AG, Product Safety Department. We recommend to read carefully the material safety data sheet prior to the use of our product.Packaging and storageOur products are inert and extremely stable chemically. However, due to their high specific surface area, they can absorb moisture and volatile organic compounds from the surrounding atmosphere. Therefore, we recommend to store the products in sealed containers in a dry, cool place, and removed from volatile organic substances. Even if a product is stored under these conditions, after a longer period it can still pick up ambient moisture over time, which could lead to its exceeding the specified moisture content. For this reason, our recommended use­by date is 24 months after date of manufacture. Product more than 24 months old should be tested for moisture content before use in order to make certain that it is still suitable for the intended application.ACEMATT TS 100 is a fumed silica that is not surface treated. This matting agent is distinguished by excellent matting efficiency combined with the highest transparency. Thanks to its unique property profile, it is particularly suitable for coatings that are not easily matted. Particularly noteworthy is its use in water-based coatings, waterborne UV-coatings,clear coatings, and coatings for leather, artificial leather, and foils, as well as top coats of all types. ACEMATT TS 100 allows formulation of coatings with outstanding resistance to household chemicals. Due to its high purity and extremely low electrical conductivity, ACEMATT TS 100 is excellently suited for use in correspondingly sensitive coating systems such as solder resist. An experiment was conducted with different amounts of TEOS, matting agent (Degussa Acematt TS 100), and an acrylate type UV cure resin that cures to 100% solids. A coating of each solution was prepared on aluminum using an RDS number 3 coating rod to produce a coating thickness of approximately 0.25 mil and the coating was UV cured for 30 seconds with a Panacol-Elosol UV-H255 instrument at a wavelength of 300-400 nm. Gloss was measured with a Rhopoint NOVO-HAZE hazemeter on 6 locations, which were averaged to produce the Avg. Gloss reading. Only solutions containing both TEOS and matting agent produced low (<100) gloss.An experiment was conducted with and without TEOS, matting agent (Degussa ACEMATT TS 100), and a urethane (meth)acrylate type UV cure resin, Dymax 9-20557 that cures to 100% solids. A coating of each solution was prepared on paper using an RDS number 3 coating rod to produce a coating thickness of approximately 0.25 mil and the coating was UV cured for 30 seconds with a PANACOL-ELOSOL UV-H255 instrument at a wavelength of 300-400 nm. Gloss was measured with a Rhopoint NOVO-HAZE hazemeter on 6 locations, which were averaged to produce the Avg. Gloss reading. A significant reduction in haze was observed when TEOS and TS 100 were added to the resin as opposed to TS 100 alone.An experiment was conducted with and without TEOS, matting agent (Degussa ACEMATT TS100), and a urethane-(meth)acrylate type UV cure resin, Dymax 984-LVUF that cures to 100% solids. This resin is lower in viscosity than in example 14. A coating of each solution was prepared on paper using an RDS number 3 coating rod to produce a coating thickness of approximately 0.25 mil and the coating was UV cured for 30 seconds with a PANACOL-ELOSOL UV-H255 instrument at a wavelength of 300-400 nm. Gloss was measured with a Rhopoint NOVO-HAZE hazemeter on 6 locations, which were averaged to produce the Avg. Gloss reading. A significant reduction in haze was observed when TEOS and TS100 were added to the resin, although TS 100 alone was almost as good.ACEMATT TS 100 is an untreated thermal silica characterised by very high matting efficiency combined with very high transparency. It can be used in water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats.ACEMATT TS 100/20 is an untreated thermal silica characterised by very high matting efficiency combined with high transparency. The particle size distribution in ACEMATT TS 100/20 is slightly broader than in ACEMATT TS 100.Thanks to the unique properties ACEMATT TS 100/20 is particularly suitable for coating systems that are difficult to matt.Special application areas include: water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACEMATT TS 100/20 show outstanding resistance against household chemicals.ACEMATT TS 100/20 improves flow behavior and increases storage stability in powder coatings.ACEMATT TS 100 Matting agents are high performance silica developed for a variety of applications in Paints & Coatings.ACEMATT TS 100 is an untreated thermal silica characterised by very high matting efficiency combined with very high transparency. Thanks to the unique properties ACEMATT TS 100 is particularly suitable for coating systems that are difficult to matte. Properties and applications ACEMATT TS 100 can be used in water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACEMATT TS 100 show outstanding resistance against household chemicals. ACEMATT TS 100 improves flow behavior and increases storage stability in powder coatings. Safety and handling Information concerning the safety of this product is listed in the corresponding Safety Data Sheet, which will be sent with the first delivery or upon updating. Such information is also available from. We recommend to read carefully the material safety data sheet prior to the use of our product.Packaging and storage.For details regarding our packaging options for this product,please contact your local sales representative.Our products are inert and extremely stable chemically.However, due to their high specific surface area, they can absorb moisture and volatile organic compounds from the surrounding atmosphere. Therefore, we recommend to store the products in sealed containers in a dry, cool place, and removed from volatile organic substances. Even if a product is stored under these conditions, after a longer period it can still pick up ambient moisture over time, which could lead to its exceeding the specified moisture content. For this reason, our recommended use-by date is 24 months after date of manufacture. Product more than 24 months old should be tested for moisture content before use in order to make certain that it is still suitable for the intended application.ACEMATT TS 100 ACEMATT TS 100 is an untreated thermal silica characterised by very high matting efficiency combined with very high transparency. Thanks to the unique properties ACEMATT TS 100 is particularly suitable for coating systems that are difficult to matte.SCOPE OF APPLICATION ACEMATT TS 100 can be used in water-based coatings, waterborne UV coatings, clear coatings, coatings for leather and films, as well as all types of top coats. Coating formulations containing ACEMATT TS 100 show outstanding resistance against household chemicals.ACEMATT TS 100 improves flow behavior and increases storage stability in powder coatings.Thermal, untreated matting agent.Average agglomerate particle size (median TEM): 4 µm The chemical compound silicon dioxide, also known as silica (from the Latin silex),is an oxide of silicon with a chemical formula of SiO2 and has been known for its hardness since antiquity.Silica is most commonly found in nature as sand or quartz, as well as in the cell walls of diatoms. It is a principal component of most types of glass and substances such as concrete. Silica is the most abundant mineral in the earth's crust.ACEMATT TS 100 features excellent matting efficiency and transparency. Because of the unique manufactoring process, it is particularly suitable for systems wich are difficult to matt, for water-borne dispersion coatings and for finish coatings. Use of ACEMATT TS 100 may provide coatings with outstanding resistance to household chemicals. Thanks to the high purity and the resulting low conductivity ACEMATT TS 100 is ideal for use in sensitive coating systems. ACEMATT TS 100 improves flow behavior and the storage stability of powder coatings.Silicon dioxide, also known as silica, is an oxide of silicon with the chemical formula SiO2, most commonly found in nature as quartz and in various living organisms.In many parts of the world, silica is the major constituent of sand. Silica is one of the most complex and most abundant families of materials, existing as a compound of several minerals and as synthetic product. Notable examples include fused quartz, fumed silica, silica gel, and aerogels. It is used in structural materials, microelectronics (as an electrical insulator), and as components in the food and pharmaceutical industries.Inhaling finely divided crystalline silica is toxic and can lead to severe inflammation of the lung tissue, silicosis, bronchitis, lung cancer, and systemic autoimmune diseases, such as lupus and rheumatoid arthritis. Inhalation of amorphous silicon dioxide, in high doses, leads to non-permanent short-term inflammation, where all effects heal.In the majority of silicates, the silicon atom shows tetrahedral coordination, with four oxygen atoms surrounding a central Si atom. The most common example is seen in the quartz polymorphs. It is a 3 dimensional network solid in which each silicon atom is covalently bonded in a tetrahedral manner to 4 oxygen atoms.For example, in the unit cell of α-quartz, the central tetrahedron shares all four of its corner O atoms, the two face-centered tetrahedra share two of their corner O atoms, and the four edge-centered tetrahedra share just one of their O atoms with other SiO4 tetrahedra. This leaves a net average of 12 out of 24 total vertices for that portion of the seven SiO4 tetrahedra that are considered to be a part of the unit cell for silica (see 3-D Unit Cell).SiO2 has a number of distinct crystalline forms (polymorphs) in addition to amorphous forms. With the exception of stishovite and fibrous silica, all of the crystalline forms involve tetrahedral SiO4 units linked together by shared vertices. Silicon–oxygen bond lengths vary between the various crystal forms; for example in α-quartz the bond length is 161 pm, whereas in α-tridymite it is in the range 154–171 pm. The Si-O-Si angle also varies between a low value of 140° in α-tridymite, up to 180° in β-tridymite. In α-quartz, the Si-O-Si angle is 144°.Fibrous silica has a structure similar to that of SiS2 with chains of edge-sharing SiO4 tetrahedra. Stishovite, the higher-pressure form, in contrast, has a rutile-like structure where silicon is 6-coordinate. The density of stishovite is 4.287 g/cm3, which compares to α-quartz, the densest of the low-pressure forms, which has a density of 2.648 g/cm3.The difference in density can be ascribed to the increase in coordination as the six shortest Si-O bond lengths in stishovite (four Si-O bond lengths of 176 pm and two others of 181 pm) are greater than the Si-O bond length (161 pm) in α-quartz. The change in the coordination increases the ionicity of the Si-O bond.More importantly, any deviations from these standard parameters constitute microstructural differences or variations, which represent an approach to an amorphous, vitreous, or glassy solid.The only stable form under normal conditions is alpha quartz, in which crystalline silicon dioxide is usually encountered. In nature, impurities in crystalline α-quartz can give rise to colors (see list). The high-temperature minerals, cristobalite and tridymite, have both lower densities and indices of refraction than quartz. Since the composition is identical, the reason for the discrepancies must be in the increased spacing in the high-temperature minerals. As is common with many substances, the higher the temperature, the farther apart the atoms are, due to the increased vibration energy.[citation needed]The transformation from α-quartz to beta-quartz takes place abruptly at 573 °C. Since the transformation is accompanied by a significant change in volume, it can easily induce fracturing of ceramics or rocks passing through this temperature limit.The high-pressure minerals, seifertite, stishovite, and coesite, though, have higher densities and indices of refraction than quartz. This is probably due to the intense compression of the atoms occurring during their formation, resulting in more condensed structure.Faujasite silica is another form of crystalline silica. It is obtained by dealumination of a low-sodium, ultra-stable Y zeolite with combined acid and thermal treatment. The resulting product contains over 99% silica, and has high crystallinity and surface area (over 800 m2/g). Faujasite-silica has very high thermal and acid stability. For example, it maintains a high degree of long-range molecular order or crystallinity even after boiling in concentrated hydrochloric acid.Molten silica exhibits several peculiar physical characteristics that are similar to those observed in liquid water: negative temperature expansion, density maximum at temperatures ~5000 °C, and a heat capacity minimum. Its density decreases from 2.08 g/cm3 at 1950 °C to 2.03 g/cm3 at 2200 °C.Molecular SiO2 with a linear structure is produced when molecular silicon monoxide, SiO, is condensed in an argon matrix cooled with helium along with oxygen atoms generated by microwave discharge. Dimeric silicon dioxide, (SiO2)2 has been prepared by reacting O2 with matrix isolated dimeric silicon monoxide, (Si2O2). In dimeric silicon dioxide there are two oxygen atoms bridging between the silicon atoms with an Si-O-Si angle of 94° and bond length of 164.6 pm and the terminal Si-O bond length is 150.2 pm. The Si-O bond length is 148.3 pm, which compares with the length of 161 pm in α-quartz. The bond energy is estimated at 621.7 kJ/mol.Even though it is poorly soluble, silica occurs in many plants. Plant materials with high silica phytolith content appear to be of importance to grazing animals, from chewing insects to ungulates. Silica accelerates tooth wear, and high levels of silica in plants frequently eaten by herbivores may have developed as a defense mechanism against predation.Silica is also the primary component of rice husk ash, which is used, for example, in filtration and cement manufacturing.For well over a billion years, silicification in and by cells has been common in the biological world. In the modern world it occurs in bacteria, single-celled organisms, plants, and animals (invertebrates and vertebrates). Prominent examples include:Tests or frustules (i.e. shells) of diatoms, Radiolaria, and testate amoebae.Silica phytoliths in the cells of many plants, including Equisetaceae, practically all grasses, and a wide range of dicotyledons.The spicules forming the skeleton of many sponges.Crystalline minerals formed in the physiological environment often show exceptional physical properties (e.g., strength, hardness, fracture toughness) and tend to form hierarchical structures that exhibit microstructural order over a range of scales. The minerals are crystallized from an environment that is undersaturated with respect to silicon, and under conditions of neutral pH and low temperature (0–40 °C).Formation of the mineral may occur either within the cell wall of an organism (such as with phytoliths), or outside the cell wall, as typically happens with tests. Specific biochemical reactions exist for mineral deposition. Such reactions include those that involve lipids, proteins, and carbohydrates.It is unclear in what ways silica is important in the nutrition of animals. This field of research is challenging because silica is ubiquitous and in most circumstances dissolves in trace quantities only. All the same it certainly does occur in the living body, creating the challenge of creating silica-free controls for purposes of research. This makes it difficult to be sure when the silica present has had operative beneficial effects, and when its presence is coincidental, or even harmful. The current consensus is that it certainly seems important in the growth, strength, and management of many connective tissues. This is true not only for hard connective tissues such as bone and tooth but possibly in the biochemistry of the subcellular enzyme-containing structures as well.Structural use About 95% of the commercial use of silicon dioxide (sand) occurs in the construction industry, e.g. for the production of concrete (Portland cement concrete).Certain deposits of silica sand, with desirable particle size and shape and desirable clay and other mineral content, were important for sand casting of metallic products.The high melting point of silica enables it to be used in such applications such as iron casting; modern sand casting sometimes uses other minerals for other reasons.Crystalline silica is used in hydraulic fracturing of formations which contain tight oil and shale gas.Precursor to glass and silicon Silica is the primary ingredient in the production of most glass. As other minerals are melted with silica, the principle of Freezing Point Depression lowers the melting point of the mixture and increases fluidity. The glass transition temperature of pure SiO2 is about 1475 K.When molten silicon dioxide SiO2 is rapidly cooled, it does not crystallize, but solidifies as a glass. Because of this, most ceramic glazes have silica as the main ingredient.The structural geometry of silicon and oxygen in glass is similar to that in quartz and most other crystalline forms of silicon and oxygen with silicon surrounded by regular tetrahedra of oxygen centers. The difference between the glass and crystalline forms arises from the connectivity of the tetrahedral units: Although there is no long range periodicity in the glassy network ordering remains at length scales well beyond the SiO bond length. One example of this ordering is the preference to form rings of 6-tetrahedra.The majority of optical fibers for telecommunication are also made from silica. It is a primary raw material for many ceramics such as earthenware, stoneware, and porcelain.Silicon dioxide is used to produce elemental silicon. The process involves carbothermic reduction in an electric arc furnace:Food, cosmetic, and pharmaceutical applications Silica, either colloidal, precipitated, or pyrogenic fumed, is a common additive in food production. It is used primarily as a flow or anti-caking agent in powdered foods such as spices and non-dairy coffee creamer, or powders to be formed into pharmaceutical tablets.It can adsorb water in hygroscopic applications. Colloidal silica is used as a fining agent for wine, beer, and juice, with the E number reference E551.In cosmetics, silica is useful for its light-diffusing properties and natural absorbency.Diatomaceous earth, a mined product, has been used in food and cosmetics for centuries. It consists of the silica shells of microscopic diatoms; in a less processed form it was sold as "tooth powder".[citation needed] Manufactured or mined hydrated silica is used as the hard abrasive in toothpaste.
ACEMATT TS 100

Acematt TS 100 is an untreated thermal silica with outstanding properties.
Acematt TS 100 provides veryhigh efficiencyand transparency.
Acematt TS 100 can be used in a largevarietyof coatings.

CAS Number: 112945-52



APPLICATIONS


Acematt TS 100, with CAS number 112945-52, is a chemical that is primarily used as a matting agent in various coating formulations.
Matting agents are substances added to coatings to reduce gloss and create a matte or satin finish.
Here are some applications of Acematt TS 100:

Paints and Coatings:
Acematt TS 100 is commonly used in paints, varnishes, and coatings, including architectural coatings, industrial coatings, automotive coatings, and wood coatings.
Acematt TS 100 helps in achieving a matte or low-gloss appearance in these coatings.

Printing Inks:
Acematt TS 100 is also utilized in printing inks, such as inks used for packaging materials, labels, and publications.
Acematt TS 100 aids in reducing the gloss and improving the print quality.

Plastics:
Acematt TS 100 finds applications in various plastic products and formulations.
Acematt TS 100 is used to provide a matte surface finish to plastic films, sheets, molded parts, and other plastic components.

Adhesives and Sealants:
Acematt TS 100 can be incorporated into adhesives and sealants to reduce their glossiness and create a more aesthetically pleasing appearance.


Typical Applications of Acematt TS 100:

Car OEM coatings
Wood coatings
Plasticcoatings
Leather coatings


Acematt TS 100 is a fumed silica that is not surface treated.
This matting agent is distinguished by excellent matting efficiency combined with the highest transparency.
Thanks to its unique property profile, it is particularly suitable for coatings that are not easily matted.

Particularly noteworthy is its use in water-based coatings, waterborne UV-coatings, clear coatings, and coatings for leather, artificial leather, and foils, as well as top coats of all types.
Acematt TS 100 allows formulation of coatings with outstanding resistance to household chemicals.

Due to its high purity and extremely low electrical conductivity, Acematt TS 100 is excellently suited for use in correspondingly sensitive coating systems such as solder resist.
Acematt TS 100 improves flow behavior and increases storage stability in powder coatings

Acematt TS 100 is a high performance matting agent adding versatility to your nail polish formulations.
Only low levels of addition give a matt or crackle finish.
Acematt TS 100, which is a fumed silica is listed with the INCI name 'Silica'.

Acematt TS 100 is widely used as a matting agent in various coating formulations.
Acematt TS 100 finds applications in architectural coatings, providing a matte finish to walls and surfaces.

Acematt TS 100 is commonly used in automotive coatings, contributing to a low-gloss appearance on vehicles.
Acematt TS 100 is utilized in wood coatings to achieve a matte or satin finish on wooden surfaces.
Acematt TS 100 is added to industrial coatings, such as machinery and equipment coatings, to reduce glossiness.

Acematt TS 100 is incorporated into printing inks to enhance print quality and reduce gloss in packaging materials.
Acematt TS 100 is used in the production of labels, providing a matte appearance on printed labels.

Acematt TS 100 is utilized in publications, such as magazines and books, to reduce glare and create a pleasant reading experience.
Acematt TS 100 is added to plastic films to create a matte surface finish in applications like packaging.

Acematt TS 100 is used in plastic sheets to provide a non-reflective surface suitable for various purposes.
Acematt TS 100 finds applications in molded plastic parts, such as automotive interior components, where a matte finish is desired.
Acematt TS 100 is incorporated into adhesives to reduce the glossiness of bonded surfaces.

Acematt TS 100 is used in sealants, such as silicone sealants, to achieve a matte appearance when applied.
Acematt TS 100 finds applications in furniture coatings, providing a low-gloss finish on wooden furniture.

Acematt TS 100 is added to metal coatings to reduce the gloss and create a visually appealing surface on metal objects.
Acematt TS 100 is utilized in coil coatings for metal sheets, contributing to a matte or satin finish.

Acematt TS 100 finds applications in floor coatings, providing a non-slip, low-gloss surface on floors.
Acematt TS 100 is used in roof coatings to achieve a matte appearance on roofing materials.

Acematt TS 100 is incorporated into can coatings, reducing the glossiness of metal cans used for packaging.
Acematt TS 100 finds applications in plastic automotive parts, providing a low-gloss finish in interior and exterior components.
Acematt TS 100 is added to powder coatings, contributing to a matte or satin appearance on coated surfaces.

Acematt TS 100 is utilized in leather coatings, providing a non-reflective finish on leather products.
Acematt TS 100 finds applications in electronic coatings, reducing glossiness on electronic components.

Acematt TS 100 is used in cosmetic packaging, providing a matte or satin appearance on containers and tubes.
Acematt TS 100 is added to ceramic coatings, contributing to a low-gloss finish on ceramic tiles and other ceramic products.

Acematt TS 100 is commonly used in the formulation of UV-curable coatings, providing a matte finish in applications such as electronics and furniture.
Acematt TS 100 finds applications in decorative coatings for glass surfaces, creating a low-gloss appearance on glassware and decorative glass items.

Acematt TS 100 is added to cosmetic formulations, including foundations, powders, and lipsticks, to achieve a matte or satin finish on the skin.
Acematt TS 100 is utilized in ceramic glazes, contributing to a matte or semi-matte surface on ceramic tiles and pottery.

Acematt TS 100 finds applications in the formulation of textile coatings, providing a low-gloss finish on fabrics and textiles.
Acematt TS 100 is added to concrete sealers to create a matte appearance on concrete surfaces while maintaining their durability and protection.
Acematt TS 100 is used in the production of anti-reflective coatings for eyeglasses and optical lenses, reducing glare and improving visual clarity.

Acematt TS 100 finds applications in graphic arts, such as inks for screen printing and lithography, to achieve a matte or satin finish on printed materials.
Acematt TS 100 is incorporated into powder coatings for metal surfaces, contributing to a non-reflective and aesthetically pleasing finish.

Acematt TS 100 is utilized in automotive refinishing coatings, providing a matte or satin appearance in repairs and touch-ups.
Acematt TS 100 is added to furniture polishes and waxes, creating a matte or low-gloss finish on wooden furniture.

Acematt TS 100 finds applications in photoresists for microelectronics and semiconductor manufacturing, aiding in the production of matte surfaces for lithography processes.
Acematt TS 100 is used in architectural films, providing a matte appearance on surfaces like glass, metal, and plastics in building interiors.

Acematt TS 100 is incorporated into nail polish formulations, contributing to a matte or satin finish on nails.
Acematt TS 100 finds applications in museum coatings and conservation materials, providing a non-reflective finish on artifacts and artwork displays.
Acematt TS 100 is utilized in the production of matte photo papers, creating a smooth and non-glossy surface for printing photographs.

Acematt TS 100 is added to plastic packaging materials, such as blister packs and clamshells, to reduce glossiness and improve visibility of packaged products.
Acematt TS 100 finds applications in anti-fingerprint coatings for electronic devices, reducing smudges and maintaining a clean matte surface.

Acematt TS 100 is used in the formulation of touch-sensitive films and coatings, providing a matte finish on touchscreens and displays.
Acematt TS 100 is incorporated into toner formulations for laser printers, contributing to a matte appearance in printed documents and images.

Acematt TS 100 finds applications in industrial floor coatings, providing a low-gloss and anti-slip finish in warehouses, factories, and commercial spaces.
Acematt TS 100 is utilized in the production of matte vinyl films and wraps for vehicle customization and signage applications.
Acematt TS 100 is added to ceramic glazes for sanitaryware, creating a matte surface on bathroom fixtures like sinks and toilets.

Acematt TS 100 finds applications in the formulation of anti-glare coatings for eyewear and sunglasses, reducing reflections and improving visual comfort.
Acematt TS 100 is used in the production of matte paints and coatings for art and craft applications, allowing for a variety of matte effects in creative projects.



DESCRIPTION


Acematt TS 100 is an untreated thermal silica with outstanding properties.
Acematt TS 100 provides veryhigh efficiencyand transparency.
Acematt TS 100 can be used in a largevarietyof coatings.

Acematt TS 100 is highly efficient.
Acematt TS 100 has very high transparency.
Acematt TS 100 has good chemical resistance.

Acematt TS 100 is a high performance matting agent adding versatility to your nail polish formulations.
Only low levels of addition give a matt or crackle finish.
Acematt TS 100, which is a fumed silica is listed with the INCI name 'Silica'.



PROPERTIES


Appearance:
Physical state: solid
Form: Powder
Color: White
Odor: Odorless
Odor Threshold: Not applicable
Melting Point: Approximate 3,092 °F/1,700 °C
Boiling Point: No data available.
Flammability:
Not applicable
Upper/lower limit on flammability or explosive limits
Explosive limit - upper: Not applicable
Explosive limit - lower: Not applicable
Flash Point: Not applicable (solid)
Self Ignition Temperature: Not applicable
Decomposition Temperature: > 3,092 °F/> 1,700 °C
pH: Approximate 6.5 (DIN / ISO 787 / 9) (50 g/l, 20 °C)
Suspension
Viscosity
Dynamic viscosity: Not applicable (solid)
Kinematic viscosity: Not applicable (solid)
Flow Time: No data available.
Solubility(ies)
Solubility in Water: > 1 mg/l
Solubility (other): No data available.
Partition coefficient (noctanol/water):
Not applicable
Vapor pressure: Not applicable
Relative density: No data available.
Density: Approximate 2.2 g/cm3 (68 °F/20 °C) (DIN / ISO 787 / 10)
Bulk density: No data available.
Vapor density (air=1): No data available.
Other information
Explosive properties: Not to be expected in view of the structure
Oxidizing properties: Not to be expected in view of the structure
Minimum ignition temperature: Not applicable
Peroxides: Not applicable
Dust explosion properties: Not dust explosive
Evaporation Rate: Not applicable
Minimum ignition energy: Not applicable



FIRST AID


Inhalation:

In case product dust is released:

Possible discomfort: cough, sneezing
Move to fresh air.

Skin Contact:
Wash off with plenty of water and soap.

Eye contact:
In case of contact, immediately flush eyes with plenty of water for at least 15 minutes or until all material has been removed.
Obtain medical attention.
No information available.

Ingestion:
Clean mouth with water and drink afterwards plenty of water.

In case of discomfort: Supply with medical care.



HANDLING AND STORAGE


Handling:

Technical measures (e.g. Local and general ventilation):
Ensure adequate ventilation, especially in confined areas.

Safe handling advice:
Handle in accordance with good industrial hygiene and safety practice.
If there is the possibility of skin/eye contact, the indicated hand/eye/body protection should be used.
If workplace exposure limits are exceeded and/or larger amounts are released (leakage, spilling, dust) the indicated respiratory protection should be used.
Use with adequate ventilation.

Contact avoidance measures:
No data available.


Storage

Safe storage conditions:
Take precautionary measures against static discharges.
Keep containers tightly sealed and store in a dry, cool place

Safe packaging materials:
No data available.



SYNONYMS


Silica Matting Agents
Silica-based Matting Agents
Fumed Silica Matting Agents
Amorphous Silica Matting Agents
Matting Silica Additives
Silica-based Matting Agents
Silica Gel Matting Agents
Silica Microspheres
Polymeric Matting Agents
Organic Matting Agents
Wax-based Matting Agents
Nylon-based Matting Agents
Polymer Microspheres
Acrylic Matting Agents
Polyurethane Matting Agents
Alumina Matting Agents
Talc Matting Agents
MatSil™ TS 100
MatTex™ TS 100
ACEROLA CHERRY EXTRACT

Acerola Cherry Extract is a natural, vitamin C-rich ingredient derived from the Acerola cherry, known for its powerful antioxidant properties and skin-brightening effects.
Acerola Cherry Extract is recognized for its ability to protect the skin from oxidative stress, promote collagen production, and enhance skin radiance, making it a popular choice in skincare formulations.
This versatile extract offers both protective and rejuvenating benefits, helping to maintain youthful, vibrant, and healthy-looking skin.

CAS Number: 84625-32-1
EC Number: 283-626-9

Synonyms: Acerola Cherry Extract, Malpighia Glabra Fruit Extract, Acerola Fruit Extract, Acerola Vitamin C Extract, Acerola Antioxidant Extract, Acerola Cherry Powder, Acerola Cherry Juice Extract, Acerola Skin Brightening Extract, Acerola Cherry Active, Acerola Fruit Juice Extract, Acerola Phytoextract, Acerola Bioactive Complex, Acerola Cherry Concentrate, Acerola Berry Extract, Acerola Natural Extract, Acerola Skin Care Active, Acerola Vitamin Complex, Acerola Brightening Agent, Acerola Anti-Aging Extract, Acerola Cherry Phytocomplex



APPLICATIONS


Acerola Cherry Extract is extensively used in the formulation of anti-aging creams, providing powerful antioxidant protection that helps to reduce the appearance of fine lines and wrinkles.
Acerola Cherry Extract is favored in the creation of serums, where it delivers concentrated vitamin C benefits that enhance skin radiance and support collagen synthesis.
Acerola Cherry Extract is utilized in the development of brightening treatments, helping to even skin tone and reduce the appearance of dark spots.

Acerola Cherry Extract is widely used in the production of moisturizing creams, offering hydration and antioxidant protection for dry and mature skin.
Acerola Cherry Extract is employed in the formulation of sunscreens, providing additional protection against UV-induced damage while enhancing overall skin resilience.
Acerola Cherry Extract is essential in the creation of facial oils, offering a blend of nourishing and protective benefits that enhance skin health and vitality.

Acerola Cherry Extract is utilized in the production of eye creams, providing targeted antioxidant care that reduces puffiness, dark circles, and signs of aging around the eyes.
Acerola Cherry Extract is a key ingredient in the formulation of after-sun products, providing soothing and protective benefits to sun-exposed skin.
Acerola Cherry Extract is used in the creation of protective serums, where it strengthens the skin's natural defenses against environmental aggressors.

Acerola Cherry Extract is applied in the formulation of face masks, providing intensive antioxidant care that revitalizes and refreshes the skin.
Acerola Cherry Extract is employed in the production of body lotions, offering all-over antioxidant protection and promoting skin firmness and elasticity.
Acerola Cherry Extract is used in the development of anti-pollution skincare products, providing a protective barrier against environmental pollutants while enhancing skin radiance.

Acerola Cherry Extract is widely utilized in the formulation of scalp treatments, providing antioxidant protection that supports scalp health and promotes stronger hair.
Acerola Cherry Extract is a key component in the creation of anti-inflammatory skincare products, offering soothing and protective benefits for sensitive skin.
Acerola Cherry Extract is used in the production of lip care products, providing antioxidant protection and hydration for soft, smooth lips.

Acerola Cherry Extract is employed in the formulation of prebiotic skincare products, supporting the skin’s microbiome while providing powerful antioxidant benefits.
Acerola Cherry Extract is applied in the creation of hand creams, offering antioxidant protection that helps to maintain skin softness and reduce signs of aging on the hands.
Acerola Cherry Extract is utilized in the development of daily wear creams, offering balanced hydration, protection, and anti-aging benefits for everyday use.

Acerola Cherry Extract is found in the formulation of skin repair treatments, providing intensive care that helps to restore and protect damaged or aging skin.
Acerola Cherry Extract is used in the production of facial mists, offering a refreshing boost of antioxidant protection throughout the day.
Acerola Cherry Extract is a key ingredient in the creation of soothing gels, providing antioxidant care that calms and protects sensitive skin.

Acerola Cherry Extract is widely used in the formulation of multipurpose balms, providing versatile care for sensitive areas such as lips, hands, and face.
Acerola Cherry Extract is employed in the development of nourishing body butters, offering rich hydration and antioxidant protection for dry, rough skin.
Acerola Cherry Extract is applied in the production of anti-aging serums, offering deep antioxidant protection that helps to maintain youthful-looking skin.

Acerola Cherry Extract is utilized in the creation of facial oils, offering nourishing care that supports skin health and reduces oxidative stress.
Acerola Cherry Extract is found in the formulation of sensitive skin repair treatments, providing targeted care for areas prone to irritation and discomfort.
Acerola Cherry Extract is used in the production of sun care products, providing protection against UV rays while offering antioxidant care that preserves skin health.



DESCRIPTION


Acerola Cherry Extract is a natural, vitamin C-rich ingredient derived from the Acerola cherry, known for its powerful antioxidant properties and skin-brightening effects.
Acerola Cherry Extract is recognized for its ability to protect the skin from oxidative stress, promote collagen production, and enhance skin radiance, making it a popular choice in skincare formulations.

Acerola Cherry Extract offers additional benefits such as enhancing skin resilience and improving overall skin texture, ensuring long-lasting protection and radiance.
Acerola Cherry Extract is often incorporated into formulations designed to provide comprehensive protection against environmental damage, offering both immediate and long-term benefits.
Acerola Cherry Extract is recognized for its ability to enhance the overall health and appearance of the skin, leaving it smooth, vibrant, and youthful-looking.

Acerola Cherry Extract is commonly used in both traditional and innovative skincare formulations, providing a reliable solution for protecting and preserving skin health.
Acerola Cherry Extract is valued for its ability to support the skin's natural defenses, making it a key ingredient in products that aim to protect the skin from environmental aggressors.
Acerola Cherry Extract is a versatile ingredient that can be used in a variety of products, including creams, serums, oils, and lotions.

Acerola Cherry Extract is an ideal choice for products targeting aging, stressed, and environmentally exposed skin, as it provides gentle yet effective protection and rejuvenation.
Acerola Cherry Extract is known for its compatibility with other skincare actives, allowing it to be easily integrated into multi-functional formulations.
Acerola Cherry Extract is often chosen for formulations that require a balance between protection, rejuvenation, and skin care, ensuring comprehensive care for all skin types.

Acerola Cherry Extract enhances the overall effectiveness of personal care products by providing powerful antioxidant protection, skin-enhancing effects, and environmental defense in one ingredient.
Acerola Cherry Extract is a reliable ingredient for creating products that offer a pleasant user experience, with noticeable improvements in skin health, radiance, and resilience.
Acerola Cherry Extract is an essential component in innovative skincare products that stand out in the market for their performance, safety, and ability to protect and enhance the skin.



PROPERTIES


Chemical Formula: N/A (Natural extract)
Common Name: Acerola Cherry Extract (Malpighia Glabra Fruit Extract)
Molecular Structure:
Appearance: Light yellow to orange liquid or powder
Density: Approx. 1.03-1.08 g/cm³ (for liquid extract)
Melting Point: N/A (liquid or powder form)
Solubility: Soluble in water and alcohols; insoluble in oils
Flash Point: >100°C (for liquid extract)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low (for liquid extract)



FIRST AID


Inhalation:
If Acerola Cherry Extract is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of eye contact, flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
If Acerola Cherry Extract is ingested, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of vapors.

Ventilation:
Ensure adequate ventilation when handling large amounts of Acerola Cherry Extract to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Acerola Cherry Extract.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Acerola Cherry Extract in a cool, dry, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid inhalation of vapors and direct contact with skin and eyes.
Use explosion-proof equipment in areas where vapors may be present.


Storage:

Temperature:
Store Acerola Cherry Extract at temperatures between 15-25°C as recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Acerola Cherry Extract away from incompatible materials, including strong oxidizers.

Handling Equipment:
Use dedicated equipment for handling Acerola Cherry Extract to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of cosmetic ingredients.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ACESULFAM K
Acesulfame potassium; Potassium acesulfame; Sunett;6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide potassium salt; 1,2,3-Oxathiazin-4(3H)-one, 6-methyl-, 2,2-dioxide potassium salt; 6-Methyl-1,2,3-oxathiazin-4(3H)-one-2,2-dioxide potassium; Sweet one; cas no: 55589-62-3
ACESULFAME K
Acesulfame potassium; Potassium acesulfame; Sunett; 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide potassium salt; 1,2,3-Oxathiazin-4(3H)-one, 6-methyl-, 2,2-dioxide potassium salt; 6-Methyl-1,2,3-oxathiazin-4(3H)-one-2,2-dioxide potassium; Sweet one; CAS NO:55589-62-3, 33665-90-6 (Parent)
ACESULFAME K

Acesulfame K, commonly known as Acesulfame K or Ace-K, is a calorie-free artificial sweetener used as a sugar substitute in food and beverage products.
Chemically, it is a potassium salt containing the organic compound acesulfame.
Acesulfame K is approximately 200 times sweeter than sucrose (table sugar) and is often used in combination with other sweeteners to enhance sweetness and flavor.

CAS Number: 55589-62-3
EC Number: 259-715-3

Synonyms: Acesulfame K, Ace-K, E950, Sweet One, Sunett, Sweet & Safe, Nutrinova, ACK, Acesulfamo K, Sunett Potassium, E-950, Sweet and Safe, Acesulfame K, Süss One, Twinsweet, Sinsweet, Acesulfam K, Suosweet, Sweet & Fit, Einesweet, Twinsweet K, Acesulfam Potassium, Süss One, Twinsweet, Sinsweet, Acesulfam K, Suosweet, Sweet & Fit, Einesweet, Twinsweet K, E950, Sweet One, Sunett, Sweet & Safe, Nutrinova, ACK, Acesulfamo K, Sunett Potassium, E-950, Sweet and Safe, Acesulfame K, Süss One, Twinsweet, Sinsweet, Acesulfam K, Suosweet, Sweet & Fit, Einesweet, Twinsweet K, Acesulfam Potassium, Süss One, Twinsweet, Sinsweet, Acesulfam K, Suosweet, Sweet & Fit, Einesweet, Twinsweet K.



APPLICATIONS


Acesulfame K is commonly used as a sugar substitute in food and beverage products.
Acesulfame K is often found in diet sodas, providing sweetness without the calories of traditional sugar.
Acesulfame K is used in powdered drink mixes to create low-calorie alternatives to sugary beverages.

Many sugar-free chewing gums contain Acesulfame K as a sweetening agent.
Acesulfame K is added to sugar-free desserts, such as gelatin and pudding mixes, to provide sweetness.
Acesulfame K is used in dairy products like yogurt and flavored milk to enhance sweetness.

Acesulfame K is used in tabletop sweeteners, providing a calorie-free option for sweetening coffee and tea.
Acesulfame K is used in pharmaceuticals, including chewable tablets and syrups, to improve palatability.
Acesulfame K is used in oral care products like toothpaste and mouthwash to provide sweetness without promoting tooth decay.

Acesulfame K is used in vitamin and supplement formulations to improve taste and palatability.
Acesulfame K is added to sugar-free baked goods like cookies and cakes to reduce calorie content while maintaining sweetness.
Many sugar-free candies and confections contain Acesulfame K as a sweetening agent.

Acesulfame K is used in sports and energy drinks to provide sweetness without adding extra calories.
Acesulfame K is used in flavored water beverages to enhance taste without adding sugar.

Acesulfame K is used in fruit-flavored syrups and toppings to provide sweetness without added sugars.
Many sugar-free syrups used in coffee shops and cafes contain Acesulfame K as a sweetener.

Acesulfame K is used in low-calorie fruit juices and juice blends to reduce overall sugar content.
Acesulfame K is added to sugar-free jams and preserves to provide sweetness without added sugars.
Acesulfame K is used in low-calorie salad dressings and condiments to reduce sugar content.

Many sugar-free snack bars and granola bars contain Acesulfame K as a sweetening agent.
Acesulfame K is used in low-calorie frozen desserts like ice cream and frozen yogurt.

Acesulfame K is added to sugar-free baking mixes for cookies, brownies, and muffins.
Acesulfame K is used in low-calorie fruit spreads and marmalades to reduce sugar content.

Acesulfame K is used in low-calorie sauces and marinades to provide sweetness without adding extra calories.
Acesulfame K is a versatile sweetener used in a wide variety of products to provide sweetness without the calories associated with traditional sugar.

Acesulfame K is commonly used in the production of sugar-free and low-calorie carbonated beverages.
Acesulfame K is used in flavored water enhancers to provide sweetness without adding calories.
Acesulfame K is added to sugar-free ice pops and frozen treats for sweetness.

Acesulfame K is used in low-calorie fruit-flavored gelatin desserts and snacks.
Acesulfame K is used in sugar-free whipped toppings and dessert toppings for a sweet flavor.

Acesulfame K is added to sugar-free pudding mixes and dessert mixes for sweetness.
Acesulfame K is used in low-calorie fruit-flavored syrup concentrates for beverages.

Acesulfame K is used in sugar-free flavor syrups for coffee and specialty drinks.
Acesulfame K is added to sugar-free breakfast cereals and oatmeal packets for sweetness.

Acesulfame K is used in sugar-free pancake syrups and maple-flavored toppings.
Acesulfame K is used in sugar-free baking mixes for cakes, muffins, and bread.

Acesulfame K is added to sugar-free barbecue sauces and marinades for a sweet flavor.
Acesulfame K is used in sugar-free salad dressings and vinaigrettes for sweetness.

Acesulfame K is added to sugar-free ketchup and condiments for flavor enhancement.
Acesulfame K is used in sugar-free flavored vinegar for salads and marinades.
Acesulfame K is used in sugar-free protein powders and meal replacement shakes for sweetness.

Acesulfame K is added to sugar-free cough drops and throat lozenges for flavor.
Acesulfame K is used in sugar-free vitamins and supplements for palatability.
Acesulfame K is used in sugar-free breath mints and fresheners for flavor.

Acesulfame K is added to sugar-free chewing gum for sweetness.
Acesulfame K is used in sugar-free hard candies and mints for a sweet taste.
Acesulfame K is used in sugar-free dietary supplements and nutrition bars.

Acesulfame K is added to sugar-free flavored gelatin for sweetness.
Acesulfame K is used in sugar-free flavored toothpaste for taste enhancement.
Acesulfame K is a versatile sweetener used in a wide variety of sugar-free and low-calorie products to provide sweetness without the added calories of traditional sugar.

Acesulfame K does not contribute to tooth decay and is considered tooth-friendly.
Acesulfame K has a long shelf life and does not degrade easily.
Acesulfame K is often used in combination with aspartame or sucralose to achieve desired taste profiles.

Acesulfame K is approved for use in many countries worldwide.
Acesulfame K is commonly found in soft drinks, flavored water, sports drinks, and energy drinks.

Acesulfame K is also used in dairy products like yogurt and flavored milk.
Acesulfame K is stable in acidic conditions, making it suitable for use in fruit-flavored products.
Acesulfame K is odorless and does not impart any off-flavors to foods or beverages.

Acesulfame K is often preferred by diabetics and individuals watching their calorie intake.
Acesulfame K is soluble in alcohol and other organic solvents.
Acesulfame K has a high melting point, allowing it to withstand high-temperature processing.

Acesulfame K is approved for use in a wide variety of food and beverage applications.
Acesulfame K is considered safe for consumption by regulatory agencies around the world.
Acesulfame K is a versatile and widely accepted artificial sweetener that provides sweetness without the calories of traditional sugar.



DESCRIPTION


Acesulfame K, commonly known as Acesulfame K or Ace-K, is a calorie-free artificial sweetener used as a sugar substitute in food and beverage products.
Chemically, it is a potassium salt containing the organic compound acesulfame.
Acesulfame K is approximately 200 times sweeter than sucrose (table sugar) and is often used in combination with other sweeteners to enhance sweetness and flavor.

Acesulfame K was discovered in 1967 by a German chemist named Karl Clauss, who was working for the company Hoechst AG (now part of Nutrinova).
Acesulfame K received approval for use as a food additive in the United States in 1988 and has since been approved for use in many countries worldwide.

As a high-intensity sweetener, Acesulfame K provides sweetness without contributing significant calories to foods and beverages.
Acesulfame K is heat-stable, making it suitable for use in cooking and baking, and does not promote tooth decay.
However, like other artificial sweeteners, it may have a slight aftertaste, especially at high concentrations.

Acesulfame K is commonly found in a variety of products, including soft drinks, sugar-free desserts, chewing gum, yogurt, and pharmaceuticals.
Acesulfame K is often used in combination with other sweeteners such as aspartame or sucralose to achieve desired taste profiles.
Despite some controversy and debate over its safety, numerous scientific studies and regulatory agencies, including the U.S. Food and Drug Administration (FDA) and the European Food Safety Authority (EFSA), have concluded that Acesulfame K is safe for human consumption at current levels of intake.

Acesulfame K is a white, crystalline powder.
Acesulfame K has a clean, sweet taste with no bitter aftertaste.

The texture of Acesulfame K is fine and powdery.
Acesulfame K dissolves easily in water, producing clear solutions.
Acesulfame K is highly stable under a wide range of temperatures and pH levels.

Acesulfame K is approximately 200 times sweeter than sucrose.
Acesulfame K is often used in combination with other sweeteners to enhance sweetness and flavor.

Acesulfame K is commonly found in sugar-free and low-calorie food and beverage products.
Acesulfame K is heat-stable, making it suitable for use in cooking and baking.

Acesulfame K is non-nutritive, providing no calories or carbohydrates.
Acesulfame K is resistant to fermentation by yeast and bacteria, making it suitable for use in fermented products.



PROPERTIES


Physical Properties:

Appearance: White crystalline powder or granules.
Odor: Odorless.
Taste: Intensely sweet.
Solubility: Highly soluble in water.
Melting Point: Approximately 225-250°C (437-482°F).
Boiling Point: Decomposes before boiling.
Density: Approximately 1.8 g/cm³ (20°C).
Particle Size: Typically fine powder or granules.
Hygroscopicity: Low to moderate.
Color: White to off-white.
Texture: Fine and powdery.
Crystal Structure: Crystalline, typically in a monoclinic or orthorhombic lattice.


Chemical Properties:

Chemical Formula: C4H4KNO4S.
Molecular Weight: Approximately 201.24 g/mol.
Chemical Structure: Acesulfame K is a potassium salt of the organic compound Acesulfame.
Functional Groups: Contains sulfonamide and carbonyl groups.
pKa Values: The pKa values of Acesulfame K are approximately 1.5 and 4.5.
Solubility in Organic Solvents: Insoluble in most organic solvents such as ethanol and acetone.
Stability: Acesulfame K is stable under normal storage conditions; may degrade under prolonged exposure to heat, light, or acidic conditions.
Hydrolysis: Susceptible to hydrolysis under acidic or alkaline conditions, leading to degradation into its constituent molecules.
Optical Activity: Acesulfame K is optically inactive.



FIRST AID


Inhalation Exposure:

Symptoms:
Inhalation of Acesulfame K powder or aerosols may cause irritation to the respiratory tract, including coughing, wheezing, or difficulty breathing.

Immediate Actions:
Remove the affected person to fresh air immediately, away from the source of exposure.
If breathing is difficult, provide oxygen if available and assist ventilation if necessary.
Seek medical attention promptly, especially if symptoms persist or worsen.


Skin Contact:

Symptoms:
Direct contact with Acesulfame K powder or solutions may cause mild irritation or allergic reactions in sensitive individuals.

Immediate Actions:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with mild soap and water.
Rinse skin with plenty of water for at least 15 minutes to ensure complete removal of the chemical.
If irritation persists or develops, seek medical attention for further evaluation and treatment.

Eye Contact:

Symptoms:
Contact with Acesulfame K powder or solutions may cause irritation, redness, tearing, or blurred vision.

Immediate Actions:
Flush the eyes with gently flowing water for at least 15 minutes, holding the eyelids open to ensure thorough rinsing.
Remove contact lenses, if present and easily removable, during rinsing.
Seek immediate medical attention for further evaluation and treatment, even if symptoms appear mild.


Ingestion:

Symptoms:
Ingestion of Acesulfame K powder or solutions is unlikely to cause significant adverse effects.

Immediate Actions:
Do not induce vomiting unless instructed by medical personnel.
Rinse the mouth with water and encourage the affected person to drink water or milk to dilute any residual chemical.
Seek medical advice or assistance if large amounts are ingested or if symptoms of discomfort develop.


General Measures:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and protective clothing, when handling Acesulfame K to minimize skin and eye contact.

Ventilation:
Ensure adequate ventilation in work areas to minimize inhalation exposure to Acesulfame K dust or aerosols.

Handling Precautions:
Follow safe handling procedures outlined in safety data sheets (SDS) and product labels to minimize exposure risks.

Storage:
Store Acesulfame K products in tightly sealed containers in a cool, dry, and well-ventilated area away from incompatible substances.

Training:
Provide training to personnel on the safe handling, storage, and use of Acesulfame K, including first aid procedures in case of exposure.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including chemical-resistant gloves, safety goggles, and protective clothing, when handling Acesulfame K to minimize skin and eye contact.
Use respiratory protection, such as a dust mask or respirator, if working with Acesulfame K in powdered form and in poorly ventilated areas.
Avoid contact with skin, eyes, and clothing. In case of contact, follow first aid procedures outlined in the safety data sheet (SDS).

Ventilation:
Ensure adequate ventilation in work areas to minimize inhalation exposure to Acesulfame K dust or aerosols.
Use local exhaust ventilation systems or fume hoods when handling powdered Acesulfame K to control airborne dust levels.
Avoid generating aerosols or dust clouds by using handling and transfer methods that minimize the release of particles into the air.

Handling Precautions:
Handle Acesulfame K with care to prevent spills or releases. Use suitable tools and equipment, such as scoops or spatulas, to transfer the material.
Avoid generating static electricity, which can cause dust accumulation and increase the risk of ignition. Ground equipment and containers as necessary.
Do not eat, drink, or smoke while handling Acesulfame K, and wash hands thoroughly after handling to prevent inadvertent ingestion.

Storage:
Store Acesulfame K products in tightly sealed containers in a cool, dry, and well-ventilated area away from sources of heat, ignition, and direct sunlight.
Keep containers tightly closed when not in use to prevent contamination and moisture absorption.
Store Acesulfame K away from incompatible substances, such as strong acids, bases, oxidizing agents, and reactive metals, to prevent chemical reactions.
Ensure storage facilities are equipped with spill containment measures, such as spill trays or bunds, to contain spills and prevent environmental contamination.
Storage:

Temperature and Humidity:
Maintain storage temperatures within recommended ranges to prevent degradation or alteration of Acesulfame K properties.
Avoid exposure to extreme temperatures or humidity, which may affect the stability and quality of the material.

Container Handling:
Use containers made of compatible materials, such as high-density polyethylene (HDPE) or glass, for storing Acesulfame K.
Check containers for signs of damage or leaks before storing and handle with care to prevent spills or accidents.
Label all containers with the chemical name, concentration, hazard warnings, and handling precautions to ensure proper identification and handling.

Segregation:
Store Acesulfame K away from food, feed, and beverages to prevent accidental contamination.
Segregate Acesulfame K from incompatible substances to prevent cross-contamination and chemical reactions.

Inventory Management:
Implement a first-in, first-out (FIFO) inventory system to ensure older stocks are used before newer ones.
Keep accurate records of inventory levels, including dates of receipt and usage, to prevent overstocking or shortages.

Security Measures:
Restrict access to storage areas containing Acesulfame K to authorized personnel only.
Implement security measures, such as locked cabinets or access controls, to prevent unauthorized access or theft.

Emergency Preparedness:
Develop and maintain emergency response plans for handling spills, leaks, or accidents involving Acesulfame K.
Ensure personnel are trained on emergency procedures and have access to emergency response equipment, such as spill kits and personal protective gear.
ACETALDEHYDE
Acetaldehyde is an organic chemical compound with the formula CH3CHO, sometimes abbreviated by chemists as MeCHO (Me=methyl).
Acetaldehyde is one of the most important aldehydes, occuring widely in nature and being produced on a large scale in industry.
Acetaldehyde occurs naturally in coffee, bread, and ripe fruit, and is produced by plants.

CAS Number: 75-07-0
EC Number: 200-836-8
Chemical formula: C2H4O
Molar mass: 44.053 g·mol−1

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Acetaldehyde is present in various plants, ripe fruits, vegetables, smoke from tobacco, gasoline and exhaust from the engine.
Acetaldehyde is commonly used as a flavouring agent and as an intermediate in alcohol metabolism in the manufacture of acetic acid, perfumes, dyes, and medicines.
The chemical formula of Acetaldehyde is CH3CHO

Acetaldehyde is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 to < 10 tonnes per annum.
Acetaldehyde is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Acetaldehyde is an organic chemical compound with the formula CH3CHO, sometimes abbreviated by chemists as MeCHO (Me=methyl).
Acetaldehyde is one of the most important aldehydes, occuring widely in nature and being produced on a large scale in industry.

Acetaldehyde occurs naturally in coffee, bread, and ripe fruit, and is produced by plants.
Acetaldehyde is also produced by the partial oxidation of ethanol and may be a contributing factor to hangovers from alcohol consumption, produced in the liver by the enzyme alcohol dehydrogenase.

Acetaldehyde is mainly used as a precursor to acetic acid.
Acetaldehyde is also an important precursor to pyridine derivates.

Nevertheless, the global market for acetaldehyde is declining.
Acetaldehyde is toxic when applied externally for prolonged periods, an irritant and a probable carcinogen.

Acetaldehyde is also called as MeCHO.
Acetaldehyde is miscible with naptha, gasoline, xylene, ether, turpentine, alcohol and benzene.

Acetaldehyde has no colour and is a flammable liquid.
Acetaldehyde has a suffocating smell.

Acetaldehyde is non-corrosive to many metals but when Acetaldehyde has a narcotic action and can cause mucous irritation.
Acetaldehyde (IUPAC systematic name ethanal) is an organic chemical compound with the formula CH3CHO, sometimes abbreviated by chemists as MeCHO (Me = methyl).

Acetaldehyde is a colorless liquid or gas, boiling near room temperature.
Acetaldehyde is one of the most important aldehydes, occurring widely in nature and being produced on a large scale in industry.

Acetaldehyde occurs naturally in coffee, bread, and ripe fruit, and is produced by plants.
Acetaldehyde is also produced by the partial oxidation of ethanol by the liver enzyme alcohol dehydrogenase and is a contributing cause of hangover after alcohol consumption.

Pathways of exposure include air, water, land, or groundwater, as well as drink and smoke.
Consumption of disulfiram inhibits acetaldehyde dehydrogenase, the enzyme responsible for the metabolism of acetaldehyde, thereby causing Acetaldehyde to build up in the body.

Acetaldehyde is an important volatile flavoring compound found in Sherry-like wines and also in many fruits.
Acetaldehyde is mainly used as a flavoring ingredient in milk products, fruit juices and soft drinks.

When you drink alcohol, your body breaks Acetaldehyde down into a chemical called acetaldehyde.
Acetaldehyde damages your DNA and prevents your body from repairing the damage.

DNA is the cell’s “instruction manual” that controls a cell’s normal growth and function.
When DNA is damaged, a cell can begin growing out of control and create a cancer tumor.
A toxic buildup of acetaldehyde can increase your cancer risk.

The International Agency for Research on Cancer (IARC) has listed acetaldehyde as a Group 1 carcinogen.
Acetaldehyde is "one of the most frequently found air toxins with cancer risk greater than one in a million".

Acetaldehyde is a clear liquid that burns easily.
Acetaldehyde has a strong, fruity odor that in high concentrations can make breathing difficult.
Also known as ethanal, acetaldehyde forms naturally in the body and in plants.

Acetaldehyde is found in nature in many foods such as ripe fruits, cheese and heated milk.
Acetaldehyde is primarily used to produce other chemicals, including acetic acid and disinfectants, drugs and perfumes.

Acetaldehyde enters your body when you breathe air containing Acetaldehyde.
Acetaldehyde can also enter your body when you eat food or drink liquid containing acetaldehyde.

When you drink alcohol, your body makes acetaldehyde when Acetaldehyde processes the alcohol.
The effect of acetaldehyde on your health depends on how much is in your body, how long you were exposed, and how often you were exposed.
The way Acetaldehyde affects you will also depend on your health.

Another factor is the condition of the environment when you were exposed.
The way Acetaldehyde affects you will also depend on your health.

Another factor is the condition of the environment when you were exposed.
Breathing acetaldehyde for short periods can hurt your lungs.
Acetaldehyde can also hurt your heart and blood vessels.

Contact with acetaldehyde liquid or vapor can hurt the skin and eyes.
Acetaldehyde is not known if breathing, drinking or eating small amounts of acetaldehyde over long periods will hurt you.

Some animal studies show that acetaldehyde can hurt a growing fetus.
Other studies on animals show that breathing acetaldehyde can severely damage the lungs and cause cancer.
Repeated exposure to acetaldehyde in the air may cause cancer in humans.

When you drink alcohol, your liver turns acetaldehyde into an acid.
Some of the acetaldehyde enters your blood, damaging your membranes and possibly causing scar tissue.

Acetaldehyde also leads to a hangover, and can result in a faster heartbeat, a headache or an upset stomach.
The brain is most affected by acetaldehyde poisoning.

Acetaldehyde causes problems with brain activity and can impair memory.
Acetaldehyde can cause amnesia, which is the inability to remember things.
This is a common effect for people who drink too much alcohol.

Acetaldehyde is a colourless, flammable liquid with a pungent and irritating odour, volatile at ambient temperature and pressure, and is found in both indoor and outdoor air.
In Environment Canada and Health Canada’s 2000 Priority Substances List Assessment Report: Acetaldehyde, Acetaldehyde was concluded that acetaldehyde is toxic under the Canadian Environmental Protection Act, 1999 (CEPA) because Acetaldehyde may be a genotoxic carcinogen; however, there was considerable uncertainty as to the actual cancer risk.

Since the publication of the report, a number of key studies have been published, including those related to the mode of action for acetaldehyde carcinogenesis.
Therefore, in order to address the uncertainty in regards to the mode of action of acetaldehyde carcinogenesis, and to more accurately determine the risk to health from levels commonly found in Canadian homes taking into account recently published scientific data, Acetaldehyde was given high priority for a full health risk assessment and development of a Residential Indoor Air Quality Guideline (RIAQG).

The present document reviews the epidemiological, toxicological, and exposure research on acetaldehyde, as well as the conclusions from a number of comprehensive reviews from internationally recognized health and environmental organizations.
The document places an emphasis on research published since the most recent comprehensive review, and proposes new short- and long-term indoor air exposure limits.

This RIAQG for acetaldehyde is intended to provide recommended exposure limits which would minimize risks to human health and support the development of actions to limit acetaldehyde emissions.
This document also shows that, when compared to the newly proposed guidelines, levels in Canadian houses do not present a health risk.

Acetaldehyde, also known as ethanal, belongs to the class of organic compounds known as short-chain aldehydes.
These are an aldehyde with a chain length containing between 2 and 5 carbon atoms.

Acetaldehyde exists in all living species, ranging from bacteria to humans.
Within humans, acetaldehyde participates in a number of enzymatic reactions.
In particular, acetaldehyde can be biosynthesized from ethanol which is mediated by the enzyme alcohol dehydrogenase 1B.

Acetaldehyde can also be converted to acetic acid by the enzyme aldehyde dehydrogenase (mitochondrial) and aldehyde dehydrogenase X (mitochondrial).
The main method of production is the oxidation of ethylene by the Wacker process, which involves oxidation of ethylene using a homogeneous palladium/copper system: 2 CH2CH2 + O2 → 2 CH3CHO.

In humans, acetaldehyde is involved in disulfiram action pathway.
Acetaldehyde is an aldehydic, ethereal, and fruity tasting compound.
Outside of the human body, acetaldehyde is found, on average, in the highest concentration in a few different foods, such as sweet oranges, pineapples, and mandarin orange (clementine, tangerine) and in a lower concentration in.

Acetaldehyde (CH3CHO), also called ethanal, an aldehyde used as a starting material in the synthesis of 1-butanol (n-butyl alcohol), ethyl acetate, perfumes, flavourings, aniline dyes, plastics, synthetic rubber, and other chemical compounds.
Acetaldehyde has been manufactured by the hydration of acetylene and by the oxidation of ethanol (ethyl alcohol).

Today the dominant process for the manufacture of acetaldehyde is the Wacker process, developed between 1957 and 1959, which catalyzes the oxidation of ethylene to acetaldehyde.
The catalyst is a two-component system consisting of palladium chloride, PdCl2, and copper chloride, CuCl2.

Pure acetaldehyde is a colourless, flammable liquid with a pungent, fruity odour; Acetaldehyde boils at 20.8 °C (69.4 °F).

Acetaldehyde is a common name of ethanal.
Acetaldehyde is an organic chemical compound with the chemical formula CH3CHO.

Acetaldehyde is also abbreviated by chemists as MeCHO where ‘Me’ means methyl.
Acetaldehyde is one of the most important aldehydes.

Acetaldehyde is being produced on a large scale in many industries.
Acetaldehyde occurs widely in nature as in coffee, bread, and ripe fruit and is produced by plants.
Acetaldehyde is also contributing to the cause of hangover after alcohol consumption.

Pathways of exposure to acetaldehyde include air, water, land, or groundwater, as well as drink and smoke.
Consumption of disulfiram inhibits acetaldehyde dehydrogenase.
Acetaldehyde is the enzyme that is responsible for the metabolism of acetaldehyde.

Acetaldehyde is easily miscible with naptha, gasoline, xylene, ether, turpentine, alcohol and benzene.
Acetaldehyde is a colourless, flammable liquid and has a suffocating smell.

Acetaldehyde is non-corrosive to many metals but when Acetaldehyde has a narcotic action, Acetaldehyde can cause mucous irritation.
Acetaldehyde was observed by the Swedish pharmacist/chemist Carl Wilhelm Scheele in the year 1774.

Acetaldehyde is a Acetaldehyde that is produced in the human body during metabolic processes, for example when the body breaks down alcohol.
Acetaldehyde often occurs in nature as a chemical by-product in plants and in many organisms.

Acetaldehyde is also a natural ingredient in many foods, such as fruit, coffee and bread.
The taste of acetaldehyde is described as fresh with a fruity but sometimes musty odour.

Acetaldehyde is widely used in the production of other industrial chemical Acetaldehyde.
Acetaldehyde is used as a solvent in the rubber, tanning and paper industries, and as a preservative for fruit and fish.
Sometimes Acetaldehyde is also used as a flavouring agent.

Acetaldehyde is a common raw material in the organic chemical industry
Acetaldehyde has a wide range of applications and is a raw material in the manufacture of many everyday products, such as paint binders, plasticisers and superabsorbents in baby nappies.

Acetaldehyde is also used in the manufacture of various types of building materials, fire protection paints, synthetic lubricants and explosives.
In the pharmaceutical industry, Acetaldehyde is used, among other things, in the manufacture of vitamins, sleeping aids and sedatives.
Acetaldehyde is also often used as a base when producing acetic acid, which is also a basic chemical with many uses.

In the food industry, Acetaldehyde is used in the manufacture of preservatives and flavourings and occurs naturally in fruit and fruit juices.
Acetaldehyde arises naturally during fermentation and is found in low levels in foodstuffs such as milk products, soy products, pickled vegetables and non-alcoholic beverages.

Sekab produces Acetaldehyde industrially by the catalytic oxidation of ethanol.
The production process takes place with renewable bioenergy in a closed-loop system and with as little toxicological effect as possible.

Acetaldehyde is a complicated chemical to handle since Acetaldehyde reacts easily with other chemicals and with the oxygen in the air.
This implies fire hazard and explosion risk and puts demands on safe handling.

Acetaldehyde has short shelf life, which puts demands on warehouse logistics.
Sekab can ensure and satisfy all of these requirements and conditions.

Acetaldehyde (CH3CHO) is a volatile compound found in wine.
Levels in various wines are listed in Table I. On average, red wines contain 30 mg/L, white 80 mg/L, and Sherries 300 mg/L.

The high levels in sherry are considered a unique feature of this wine.
At low levels acetaldehyde can contribute pleasant fruity aromas to a wine, however, at higher levels the aroma is considered a defect and is reminiscent of rotten-apples.
The threshold in wine ranges between 100-125 mg/L.

Acetaldehyde is one of the most important sensory carbonyl compounds in wine and constitutes approximately 90% of the total aldehyde content in wine.
Acetaldehyde can be formed by yeasts and acetic acid bacteria (AAB).

AAB form acetaldehyde by oxidizing ethanol.
The amount formed by yeasts varies with species, but is considered to be a leakage product of the alcoholic fermentation.

Additionally, film yeasts (important in sherry production) will oxidize ethanol to form acetaldehyde.
Oxygen, and SO2 can all impact the amount of acetaldehyde formed by yeasts.

Wines fermented in the presence of SO2 have considerably higher amounts of acetaldehyde.
This is related to SO2 resistance of certain yeasts.

In wine, acetaldehyde concentration increases with higher temperatures, though production was higher at cooler temperatures in fermented cider with Saccharomyces cereviseae.
Acetaldehyde can also be formed as a result of oxidation of phenolic compounds.
Hydrogen peroxide, a product of phenolic oxidation, will oxidize ethanol to acetaldehyde.

At wine pH (3-4), SO2 consists mainly of bisulfite (HSO3-), and small amounts of molecular (SO2) and sulfite ion (SO32-).
The bisulfite can form complexes with carbonyl compounds, predominately acetaldehyde.

The binding of acetaldehyde to bisulfite limits Acetaldehyde sensory contribution to wine.
Addition of SO2 to ‘inhibit’ acetaldehyde production may reduce the perceived aldehyde aroma character, but is most likely only masking the aroma contribution of the acetaldehyde that is present instead of actually inhibiting Acetaldehyde production.

Acetaldehyde is primarily used as an intermediate in the manufacture of a range of chemicals, perfumes, aniline dyes, plastics and synthetic rubber and in some fuel compounds.
Acetaldehyde is also used in the manufacture of disinfectants, drugs, perfumes, explosives, lacquers and varnishes, photographic chemicals, phenolic and urea resins, rubber accelerators and antioxidants, and room air deodourisers.
Acetaldehyde is also used as a synthetic flavouring Acetaldehyde, food preservative and as a fragrance.

Acetaldehyde is a toxic molecule that is always circulating in the blood in low concentrations.
A Group 1 carcinogen, acetaldehyde can cause damage in our bodies and continued exposure can lead to cancer and other disease.
In our modern environment, acetaldehyde enters the body from a number of sources.

Acetaldehyde is also produced inside our own bodies through regular processes.
Those with ALDH2 Deficiency cannot properly break down acetaldehyde, which leads to accumulation in the body and increases the risk of long-term diseases.
Those with ALDH2 Deficiency should be aware of the major sources of acetaldehyde.

Acetaldehyde, produced from the metabolism of ethanol, may also be responsible for localized cancers, brain damage in prenatal infants, and growth suppression (in chicken embryos).
Acetaldehyde, as a direct result of ethanol metabolism in the body, has been implicated in alcoholic cardiomyopathy and cancer of the digestive tract.

Acetaldehyde DNA adducts have been observed in the lymphocytes of human alcohol abusers.
Esophageal tumors have been reportedly associated with genetic polymorphisms that result in high acetaldehyde levels after ethanol consumption, but there is inadequate evidence to associate carcinogenicity in humans with acetaldehyde exposure.
The levels of acetaldehyde in blood are directly correlated with ethanol consumption.

Acetaldehyde, also called ethanal, is the simplest aldehyde (CH3CHO).
Acetaldehyde is a colourless and volatile liquid made by the catalytic oxidation of ethanol, with a sharp and fruity odour.
Acetaldehyde is widely used industrially as a chemical intermediate.

Acetaldehyde is also a metabolite of sugars and ethanol in humans,is found naturally in the environment, and is a product of biomass combustion.
Acetaldehyde is primarily used as an intermediate in the manufacture of a range of chemicals, perfumes, aniline dyes, plastics and synthetic rubber and in some fuel compounds.

Acetaldehyde is an important reagent used in the manufacture of dyes, plastics, and many other organic chemicals.
In the presence of acids Acetaldehyde forms the cyclic polymers paraldehyde (CH3CHO)3, and metaldehyde (CH3CHO)4.

The former is used as a hypnotic, and the latter as a solid fuel for portable stoves and as a poison for snails and slugs.
Acetaldehyde is also used in the manufacture of disinfectants, drugs, perfumes, explosives, lacquers and varnishes, photographic chemicals, phenolic and urea resins, rubber accelerators and antioxidants, and room air deodourizers.
Acetaldehyde is also used as a synthetic flavouring Acetaldehyde, food preservative and as a fragrance.

Acetaldehyde is a highly flammable, volatile colourless liquid.
Acetaldehyde has a characteristic, pungent, and suffocating odour and is miscible in water.

Acetaldehyde is ubiquitous in the ambient environment.
Acetaldehyde is an intermediate product of higher plant respiration and formed as a product of incomplete wood combustion in fireplaces and woodstoves, burning of tobacco, vehicle exhaust fumes, coal refining, and waste processing.
Exposures to acetaldehyde occur during the production of acetic acid and various other industrial chemical Acetaldehyde, for instance, manufacture of drugs, dyes, explosives, disinfectants, phenolic and urea resins, rubber accelerators, and varnish.

Uses of Acetaldehyde:
Acetaldehyde was used as a precursor to acetic acid.
Acetaldehyde is used as a precursor to pyridine derivatives, crotonaldehyde, and pentaerythritol.

Acetaldehyde is used in the manufacturing of resin.
Acetaldehyde is used to produce polyvinyl acetate.

Acetaldehyde is used in the manufacturing of disinfectants, perfumes, and drugs.
Acetaldehyde is used in the production of chemicals such as acetic acid.

Acetaldehyde was used as a precursor to acetic acid.
Acetaldehyde was used as a precursor to pyridine derivatives, crotonaldehyde, and pentaerythritol.

Acetaldehyde is used in the manufacturing of resin.
Acetaldehyde is used to produce polyvinyl acetate.

Acetaldehyde is used in the manufacturing of disinfectants, perfumes, and drugs.
Acetaldehyde is used in the production of chemicals such as acetic acid.

Acetaldehyde is used in producing acetic acid, acetic anhydride, cellulose acetate, syntheticpyridine derivatives, pentaerythritol, terephthalicacid, and many other raw materials.
Release of acetaldehyde from poly ethyleneterephthalate (PET) bottles into carbonatedmineral waters has been observed; 180 ppm was detected in sampleskept for 6 months at 40°C (104°F).

Acetaldehyde is also known as ethanal, acetaldehyde is miscible with H2O, alcohol, or ether in all proportions.
Because of Acetaldehyde versatile chemical reactivity, acetaldehyde is widely used as a commencing material in organic syntheses, including the production of resins, dyestuffs, and explosives.

Acetaldehyde also is used as a reducing agent, preservative, and as a medium for silvering mirrors.
In resin manufacture, paraldehyde (CH3CHO)3 sometimes is preferred because of Acetaldehyde higher boiling and flash points.

Acetaldehyde is used as a general solvent in organic and polymer chemical reactions.
Acetaldehyde also plays a role in fruit and food quality, ripening and deterioration.

Manufacture of paraldehyde, acetic acid, butanol, perfumes, flavors, aniline dyes, plastics, synthetic rubber; silvering mirrors, hardening gelatin fibers.
Acetaldehyde is used as flavoring agent in foods and beverages.
Acetaldehyde is fumigant for storage of apples and strawberries.

Acetaldehyde can also be used as an odorant, and Acetaldehyde found in nature in many foods such as ripe fruits, cheese and heated milk.
Acetaldehyde occurs naturally during fermentation, and low levels of acetaldehyde are to be found in certain foods.

Acetaldehyde is mainly used for preparation of citrus, apple, cream type essence, etc.
Acetaldehyde is mostly used in acetic acid industry.

Butanol and octanol are also the important derivatives of the acetaldehyde in the past.
Nowadays, butanol and octanol are prepared by Propylene carbonyl synthesis method.

Acetaldehyde is a very important raw material in the production of a large number of chemical products, for example paint binders in alkyd paints and plasticizers for plastics.
Acetaldehyde is also used in the manufacture of construction materials, fire retardant paints and explosives, while Acetaldehyde uses within the pharmaceutical industry include the manufacture of sedatives and tranquilisers, among other things.
Acetaldehyde can also be used as a raw material in the manufacture of acetic acid, another platform chemical with many applications.

Acetaldehyde is also used to produce pentaerythritol, peracetic acid, pyridine and Acetaldehyde derivatives.
Domestically produced acetaldehyde is mainly used as intermediate for the production of acetic acid.

Only a small amount is used for the production of pentaerythritol, butanol, trichloroacetaldehyde, trimethylolpropane, etc.
The predominant use of acetaldehyde is as an intermediate in the synthesis of other chemicals.

Acetaldehyde is used in the production of perfumes, polyester resins, and basic dyes.
Acetaldehyde is also used as a fruit and fish preservative, as a flavoring agent, and as a denaturant for alcohol, in fue compositions, for hardening gelatin, and as a solvent in the rubber, tanning, and paper industries.

The predominant use of acetaldehyde is as an intermediate in the synthesis of other chemicals.

Glue sticks, glitter glues, fabric glues, craft glue, spray mounts, stencil sprays, and other adhesives used for primarily craft purposes
Cleaning and household care products that can not be placed in a more refined category

Acetaldehyde is used in synthesis of organic chemicals, resins, dyes, pesticides, disinfectants, cosmetics, gelatin, glue, lacquers, varnishes, casein products, explosives, and pharmaceuticals.
Acetaldehyde is also used as a hardener in photography, a flavoring agent, and a leather preservative.

Acetaldehyde is also used in leather tanning, in glue products, and in the paper industry.

Acetaldehyde is used in the production of acetic acid, acetic anhydride, cellulose acetate, vinyl acetate resins, acetate esters, pentaerythritol, synthetic pyridine derivatives, terephthalic acid, and peracetic acid.
Acetaldehyde is also used in the production of perfumes, polyester resins, basic dyes, in fruit and fish preservation, as a flavoring agent, an alcohol denaturant, as a hardening agent for gelatin, in fuel compositions, and as a solvent in the rubber, tanning, and paper industries.

Hydraulic fracturing uses a specially blended liquid which is pumped into a well under extreme pressure causing cracks in rock formations underground.
These cracks in the rock then allow oil and natural gas to flow, increasing resource production.
Although there are dozens to hundreds of chemicals which could be used as additives, there are a limited number which are routinely used in hydraulic fracturing.

Traditionally, acetaldehyde was mainly used as a precursor to acetic acid.
This application has declined because acetic acid is produced more efficiently from methanol by the Monsanto and Cativa processes.

Acetaldehyde is an important precursor to pyridine derivatives, pentaerythritol, and crotonaldehyde.
Urea and acetaldehyde combine to give a useful resin.
Acetic anhydride reacts with acetaldehyde to give ethylidene diacetate, a precursor to vinyl acetate, which is used to produce polyvinyl acetate.

The global market for acetaldehyde is declining.
Demand has been impacted by changes in the production of plasticizer alcohols, which has shifted because n-butyraldehyde is less often produced from acetaldehyde, instead being generated by hydroformylation of propylene.

Likewise, acetic acid, once produced from acetaldehyde, is made predominantly by the lower-cost methanol carbonylation process.
The impact on demand has led to increase in prices and thus slowdown in the market.

China is the largest consumer of acetaldehyde in the world, accounting for almost half of global consumption in 2012.
Major use has been the production of acetic acid.

Other uses such as pyridines and pentaerythritol are expected to grow faster than acetic acid, but the volumes are not large enough to offset the decline in acetic acid.
As a consequence, overall acetaldehyde consumption in China may grow slightly at 1.6% per year through 2018.

Western Europe is the second-largest consumer of acetaldehyde worldwide, accounting for 20% of world consumption in 2012.
As with China, the Western European acetaldehyde market is expected to increase only very slightly at 1% per year during 2012–2018.

However, Japan could emerge as a potential consumer for acetaldehyde in next five years due to newfound use in commercial production of butadiene.
The supply of butadiene has been volatile in Japan and the rest of Asia.
This should provide the much needed boost to the flat market, as of 2013.

Acetaldehyde is an intermediate in the production of acetic acid, acetic anhydride, cellulose acetate, vinyl acetate resins, acetate esters, pentaerythritol, synthetic pyridine derivatives, terephthalic acid and peracetic acid.
Other uses of acetaldehyde include silvering of mirrors; leather tanning; denaturant for alcohol; fuel mixtures; hardener for gelatine fibres; glue and casein products; preservative for fish and fruit; synthetic flavouring agent; paper industry; and manufacture of cosmetics, aniline dyes, plastics and synthetic rubber.
The concentration of acetaldehyde in alcoholic beverages is generally below 500 mg/l.

Low levels of acetaldehyde are also reported to occur in several essential oils.
Acetaldehyde is an intermediate product in the metabolism of ethanol and sugars and also occurs as a natural metabolite in small quantities in human blood.

In cosmetic products, two possibilities of occurrence of acetaldehyde can be distinguished:

1) Acetaldehyde is used as a fragrance/flavour ingredient in fragrance compounds used in cosmetic products.
The SCCNFP concluded in Acetaldehyde opinion of 25th May 2004 that acetaldehyde can be safely used as a fragrance/flavour ingredient at a maximum concentration of 0.0025% (25 ppm) in the fragrance compound.

2) In addition, acetaldehyde can also be found in cosmetic products in the form of unavoidable traces originating mainly through:
Plant extracts and botanical ingredients
Ethanol.

Widespread uses by professional workers:
Acetaldehyde is used in the following products: pH regulators and water treatment products and laboratory chemicals.
Acetaldehyde is used in the following areas: health services and scientific research and development.
Other release to the environment of Acetaldehyde is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Uses at industrial sites:
Acetaldehyde is used in the following products: pH regulators and water treatment products and laboratory chemicals.
Acetaldehyde is used in the following areas: health services and scientific research and development.

Acetaldehyde is used for the manufacture of: chemicals.
Release to the environment of Acetaldehyde can occur from industrial use: as an intermediate step in further manufacturing of another Acetaldehyde (use of intermediates), in processing aids at industrial sites and as processing aid.

Industry Uses:
Fuels and fuel additives
Intermediates

Consumer Uses:
Adhesives and sealants
Golf and Sports Turf
Paints and coatings
Paper products
Plastic and rubber products not covered elsewhere
Process Intermediates

Properties of Acetaldehyde:

Typical Properties:
The chemical formula of Acetaldehyde is CH3CHO and its molecular weight is 44.06 g/mol.
Acetaldehyde is a colorless, mobile liquid that is flammable and miscible with water.

Acetaldehyde has a sharp, suffocating odor, but in dilute concentrations it has a fruity, pleasant odor.
The odor threshold of acetaldehyde is 0.05 parts per million (ppm) (0.09 mg/m3).

The vapor pressure of acetaldehyde is 740 mm Hg at 20 °C and the log octanol/water partition coefficient (log Kow) is 0.43.
The molecular weight/molar mass of acetaldehyde is 44.05 grams per mole.

The density of acetaldehyde is 0.784 grams per cubic centimeter.
Additionally, the boiling temperature of acetaldehyde is 20.2oC.
The melting point of acetaldehyde is -123.5oC.

Acetaldehyde is colorless, mobile, fuming, volatile liquid or gas with a penetrating, pungent odor.
Acetaldehyde is odor threshold concentrations ranged from 1.5 ppbv to 0.21 ppmv.
Katz and Talbert (1930) reported an experimental detection odor threshold concentration of 120 μg/m3 (67 ppbv).

At low concentrations, acetaldehyde imparts a pleasant, fruity, green apple or leafy green-like flavor.
Twenty-five panelists were randomly selected for testing milk products and water for determining flavor thresholds.

Chemical Properties:
The chemical properties of acetaldehyde are similar to formaldehyde.
Acetaldehyde is a precursor in organic synthesis, especially as an electrophile.

By condensation reaction, one can gain intermediates like pentaerythritol that we can be used in organic synthesis.
Also, can be useful to produce hydroxyethyl derivatives by a reaction with a Grignard reagent.
Acetaldehyde is a building block that is in use in the synthesis of heterocycles, such as imines and pyridines.

This chemical is dangerous when exposed to heat or flame.
Acetaldehyde is sensitive to air and may undergo autopolymerization.

Acetaldehyde is also sensitive to moisture.
Upon prolonged storage, Acetaldehyde may form unstable peroxides.

Can react vigorously with acid anhydrides, alcohols, ketones, phenols, ammonia, hydrogen cyanide, hydrogen sulfide, halogens, amines phosphorous, isocyanates, strong alkalies and strong acids and is incompatible with oxidising and reducing agents.
Acetaldehyde also reacts with nitric acid, peroxides, caustic soda and soda ash.

Reactions with cobalt chloride, mercury(II)chlorate or mercury(II)perchlorate form sensitive and explosive products.
Polymerisation may occur with acetic acid.

Autoignition of vapour may occur on contact with corroded metals.
Exothermic polymerisation can occur with trace metals.

Acetaldehyde is miscible with gasoline, naptha, xylene, turpentine, ether, benzene and alcohol.
Rubber products decompose on contact with acetaldehyde, but Acetaldehyde is not corrosive to most metals.

Acetaldehyde is a highly fl ammable, volatile, colorless liquid.
Acetaldehyde has a characteristic pun- gent and suffocating odor, and is miscible in water.
Acetaldehyde is ubiquitous in the ambient environment.

Acetaldehyde is an intermediate product of higher plant respiration and formed as a product of incomplete wood combustion in fi replaces and woodstoves, burning of tobacco, vehicle exhaust fumes, coal refi ning, and waste processing.
Exposures to acetal- dehyde occur during the production of acetic acid and various other industrial chemical Acetaldehyde.
For instance, the manufacture of drugs, dyes, explosives, disinfectants, pheno- lic and urea resins, rubber accelerators, and varnish.

Acetaldehyde is a flammable, volatile, colorless liquid, or gas.
Acetaldehyde has a characteristic, penetrating, fruity odor.

Production of Acetaldehyde:
The main method of production of acetaldehyde is the oxidation of ethylene.
Acetaldehyde is done by the Wacker process.

This process involves the oxidation of ethylene by homogeneous palladium or copper system.
2CH2=CH2+O2→2CH3CHO

A small quantity of acetaldehyde can be prepared by the partial oxidation of ethanol.

Acetaldehyde is an exothermic reaction and is conducted over a silver catalyst at about 500oC to 650oC.
CH3CH2OH+1/2O2→CH3CHO+H2O

Acetaldehyde is the oldest method for the preparation of acetaldehyde.

Prior to the Wacker process and the availability of ethylene, acetaldehyde is also produced by the hydration of acetylene and is catalyzed by mercury (II) salts.
C2H2+Hg2++H2O→CH3CHO+Hg

The mechanism involves the intermediacy of vinyl alcohol that is tautomerized to acetaldehyde.
The reaction is conducted at 90oC to 95oC.
Acetaldehyde formed here is separated from water and mercury and cooled to 25oC to 30oC.

In the wet oxidation process, iron (III) sulfate is in use to reoxidize the mercury to the mercury (II) salt.
The resulting iron (II) sulfate is then oxidized in a separate reactor with nitric acid.

Traditionally, Acetaldehyde was also produced by the partial dehydrogenation of ethanol.
CH3CH2OH→CH3CHO+H2

This is an endothermic process.
Ethanol vapour is passed by a copper-based catalyst at 260oC to 290oC.

In 2003, global production was about 1 million tonnes.
Before 1962, ethanol and acetylene were the major sources of acetaldehyde.
Since then, ethylene is the dominant feedstock.

The main method of production is the oxidation of ethylene by the Wacker process, which involves oxidation of ethylene using a homogeneous palladium/copper system:
2 CH2=CH2 + O2 → 2 CH3CHO

In the 1970s, the world capacity of the Wacker-Hoechst direct oxidation process exceeded 2 million tonnes annually.

Smaller quantities can be prepared by the partial oxidation of ethanol in an exothermic reaction.

This process typically is conducted over a silver catalyst at about 500–650 °C.
CH3CH2OH + 1⁄2 O2 → CH3CHO + H2O

This method is one of the oldest routes for the industrial preparation of acetaldehyde.

Other methods:

Hydration of acetylene:
Prior to the Wacker process and the availability of cheap ethylene, acetaldehyde was produced by the hydration of acetylene.

This reaction is catalyzed by mercury(II) salts:
C2H2 + Hg2+ + H2O → CH3CHO + Hg

The mechanism involves the intermediacy of vinyl alcohol, which tautomerizes to acetaldehyde.
The reaction is conducted at 90–95 °C, and the acetaldehyde formed is separated from water and mercury and cooled to 25–30 °C.

In the wet oxidation process, iron(III) sulfate is used to reoxidize the mercury back to the mercury(II) salt.
The resulting iron(II) sulfate is oxidized in a separate reactor with nitric acid.

Dehydrogenation of ethanol:

Traditionally, acetaldehyde was produced by the partial dehydrogenation of ethanol:
CH3CH2OH → CH3CHO + H2

In this endothermic process, ethanol vapor is passed at 260–290 °C over a copper-based catalyst.
The process was once attractive because of the value of the hydrogen coproduct, but in modern times is not economically viable.

Hydroformylation of methanol:
The hydroformylation of methanol with catalysts like cobalt, nickel, or iron salts also produces acetaldehyde, although this process is of no industrial importance.
Similarly noncompetitive, acetaldehyde arises from synthesis gas with modest selectivity.

Reactions of Acetaldehyde:

Tautomerization of acetaldehyde to vinyl alcohol:
Like many other carbonyl compounds, acetaldehyde tautomerizes to give an enol:
CH3CH=O ⇌ CH2=CHOH - ∆H298,g = +42.7 kJ/mol

The equilibrium constant is 6×10−7 at room temperature, thus that the relative amount of the enol form in a sample of acetaldehyde is very small.
At room temperature, acetaldehyde (CH3CH=O) is more stable than vinyl alcohol (CH2=CHOH) by 42.7 kJ/mol: Overall the keto-enol tautomerization occurs slowly but is catalyzed by acids.

Photo-induced keto-enol tautomerization is viable under atmospheric or stratospheric conditions.
This photo-tautomerization is relevant to the earth's atmosphere, because vinyl alcohol is thought to be a precursor to carboxylic acids in the atmosphere.

Condensation reactions:
Acetaldehyde is a common electrophile in organic synthesis.
In condensation reactions, acetaldehyde is prochiral.

Acetaldehyde is used primarily as a source of the "CH3C+H(OH)" synthon in aldol and related condensation reactions.
Grignard reagents and organolithium compounds react with MeCHO to give hydroxyethyl derivatives.
In one of the more spectacular condensation reactions, three equivalents of formaldehyde add to MeCHO to give pentaerythritol, C(CH2OH)4.

In a Strecker reaction, acetaldehyde condenses with cyanide and ammonia to give, after hydrolysis, the amino acid alanine.
Acetaldehyde can condense with amines to yield imines; for example, with cyclohexylamine to give N-ethylidenecyclohexylamine.
These imines can be used to direct subsequent reactions like an aldol condensation.

Acetaldehyde is also a building block in the synthesis of heterocyclic compounds.
In one example, Acetaldehyde converts, upon treatment with ammonia, to 5-ethyl-2-methylpyridine ("aldehyde-collidine").

Manufacturing Methods of Acetaldehyde:
There is still some commercial production by the partial oxidation of ethyl alcohol and hydration of acetylene.
Acetaldehyde is also formed as a coproduct in the high temperature oxidation of butane.
A more recently developed rhodium catalyzed process produces acetaldehyde from synthesis gas as a coproduct with ethyl alcohol and acetic acid.

Acetaldehyde can producing dehydrogenation of ethanol.
Ethanol vapor is passed at 260-290 °C over a catalyst consisting of copper sponge or copper activated with chromium oxide in a tubular reactor.

A conversion of 25-50% per run is obtained.
By washing with alcohol and water, acetaldehyde and ethanol are separated from the exhaust gas, which is mainly hydrogen.

Pure acetaldehyde is obtained by distillation; the ethanol is separated from water and higher-boiling products by distillation and flows back to the reactor.
The final acetaldehyde yield is about 90%.
By products include butyric acid, crotonaldehyde, and ethyl acetate.

Oxidation of ethanol is the oldest laboratory method for preparing acetaldehyde.
In the commercial process, ethanol is oxidized catalytically with oxygen (or air) in the vapor phase.
Copper, silver, and their oxides or alloys are the most frequently used catalysts.

Acetaldehyde can producing direct oxidation of ethylene.
An aqueous solution of PdCl2 and CuCl2 is used as catalyst.

Acetaldehyde formation had already been observed in the reaction between ethylene and aqueous palladium chloride.
In the Wacker-Hoechst process, metallic palladium is reoxidized by CuCl2, which is then regenerated with oxygen.

Only a very small amount of PdCl2 is required for the conversion of ethylene.
The reaction of ethylene with palladium chloride is the rate-determining step.

In the one-stage method, an ethylene - oxygen mixture reacts with the catalyst solution.
During the reaction a stationary state is established in which "reaction" (formation of acetaldehyde and reduction of CuCl2) and "oxidation" (reoxidation of CuCl) proceed at the same rate.

This stationary state is determined by the degree of oxidation of the catalyst.
In the two-stage process the reaction is carried out with ethylene and then with oxygen in two separate reactors.

The catalyst solution is alternately reduced and oxidized.
At the same time the degree of oxidation of the catalyst changes alternately.
Air is used instead of pure oxygen for the catalyst oxidation.

General Manufacturing Information of Acetaldehyde:

Industry Processing Sectors:
All other basic organic chemical manufacturing
Petrochemical manufacturing

China is the largest consumer of acetaldehyde.
Acetaldehyde is heavily used in the production of acetic acid.

This use will be limited in the future because new plants in China will use the methanol carbonylation process.
Other uses will grow, but the volumes are not large enough to offset the volumes used in acetic acid production.
Chinese consumption is expected to grow slightly at 1.6%/yr through 2018.

Acetaldehyde can producing formation during the natural alcoholic fermentation process.
Recovery is effected by suitable fractionation, subsequent preparation of the acetaldehyde ammonia, and final treatment of the addition compound with diluted sulfuric acid.

Western Europe is the second largest consumer of acetaldehyde accounting for 20% of world consumption in 2012.
The rate of growth there is expected to be 1%/yr through 2018.

Total acetaldehyde production in western Europe on January 1, 1983 was more than 0.5 million tons, & production capacity is estimated to have been nearly 1 million tons.
Most of this was based on the catalytic oxidation of ethylene; less than 10% was based on partial oxidation of ethanol, & a very small percentage was based on the hydration of acetylene.

Acetaldehyde is produced (by oxidation of ethylene) by 7 companies in Japan.
Their combined production is est to have been 278,000 tons in 1982, down from an est 323,000 tons in 1981.
Japanese imports & exports of acetaldehyde are negligible.

Polymerization of Acetaldehyde:
The Acetaldehyde may polymerize under the influence of acids, alkaline materials, such as sodium hydroxide, in the presence of trace metals (iron) with fire or explosion hazard.

Polymeric forms of Acetaldehyde:
Three molecules of acetaldehyde condense to form "paraldehyde", a cyclic trimer containing C-O single bonds.
Similarly condensation of four molecules of acetaldehyde give the cyclic molecule metaldehyde.

Paraldehyde can be produced in good yields, using a sulfuric acid catalyst.
Metaldehyde is only obtained in a few percent yield and with cooling, often using HBr rather than H2SO4 as the catalyst.
At -40 °C in the presence of acid catalysts, polyacetaldehyde is produced.
There are two stereomers of paraldehyde and four of metaldehyde.

The German chemist Valentin Hermann Weidenbusch (1821–1893) synthesized paraldehyde in 1848 by treating acetaldehyde with acid (either sulfuric or nitric acid) and cooling to 0°C.
He found Acetaldehyde quite remarkable that when paraldehyde was heated with a trace of the same acid, the reaction went the other way, recreating acetaldehyde.

Acetal derivatives of Acetaldehyde:
Acetaldehyde forms a stable acetal upon reaction with ethanol under conditions that favor dehydration.
The product, CH3CH(OCH2CH3)2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal".
This can cause confusion as "acetal" is more commonly used to describe compounds with the functional groups RCH(OR')2 or RR'C(OR'')2 rather than referring to this specific compound – in fact, 1,1-diethoxyethane is also described as the diethyl acetal of acetaldehyde.

Precursor to vinylphosphonic acid:
Acetaldehyde is a precursor to vinylphosphonic acid, which is used to make adhesives and ion conductive membranes.

The synthesis sequence begins with a reaction with phosphorus trichloride:
PCl3 + CH3CHO → CH3CH(O−)PCl3+
CH3CH(O−)PCl3+ + 2 CH3CO2H → CH3CH(Cl)PO(OH)2 + 2 CH3COCl
CH3CH(Cl)PO(OH)2 → CH2=CHPO(OH)2 + HCl

Purification Methods of Acetaldehyde:
Acetaldehyde is usually purified by fractional distillation in a glass helices-packed column under dry N2, discarding the first portion of distillate.
Acetaldehyde is shaking for 30 minutes with NaHCO3, dried with CaSO4 and fractionally distilled at 760mm through a 70cm Vigreux column.
The middle fraction is collected and further purified by standing for 2hours at 0o with a small amount of hydroquinone (free radical inhibitor), followed by distillation.

Biochemistry of Acetaldehyde:
In the liver, the enzyme alcohol dehydrogenase oxidizes ethanol into acetaldehyde, which is then further oxidized into harmless acetic acid by acetaldehyde dehydrogenase.
These two oxidation reactions are coupled with the reduction of NAD+ to NADH.

In the brain, the enzyme catalase is primarily responsible for oxidizing ethanol to acetaldehyde, and alcohol dehydrogenase plays a minor role.
The last steps of alcoholic fermentation in bacteria, plants, and yeast involve the conversion of pyruvate into acetaldehyde and carbon dioxide by the enzyme pyruvate decarboxylase, followed by the conversion of acetaldehyde into ethanol.
The latter reaction is again catalyzed by an alcohol dehydrogenase, now operating in the opposite direction.

Human Metabolite Information of Acetaldehyde:

Tissue Locations:
Adrenal Medulla
Brain
Epidermis
Erythrocyte
Fibroblasts
Intestine
Kidney
Liver
Neuron
Ovary
Pancreas
Placenta
Platelet
Skeletal Muscle
Testis
Thyroid Gland

Cellular Locations:
Cytoplasm
Endoplasmic reticulum
Extracellular
Mitochondria
Peroxisome

History of Acetaldehyde:
Acetaldehyde was first observed by the Swedish pharmacist/chemist Carl Wilhelm Scheele (1774); Acetaldehyde was then investigated by the French chemists Antoine François, comte de Fourcroy and Louis Nicolas Vauquelin (1800), and the German chemists Johann Wolfgang Döbereiner (1821, 1822, 1832) and Justus von Liebig (1835).
In 1835, Liebig named Acetaldehyde "aldehyde"; the name was later altered to "acetaldehyde".

Handling and Storage of Acetaldehyde:

Nonfire Spill Response of Acetaldehyde:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area).
All equipment used when handling Acetaldehyde must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Acetaldehyde without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Safe Storage of Acetaldehyde:
Fireproof.
Separated from incompatible materials.

Keep in the dark.
Store only if stabilized.

Acetaldehyde should be used only in areas free of ignition sources, and quantities greater than 1 liter should be stored in tightly sealed metal containers in areas separate from oxidizers.
Acetaldehyde should always be stored under an inert atmosphere of nitrogen or argon to prevent autoxidation.

Storage Conditions of Acetaldehyde:

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Recommended storage temperature: 2 - 8 °C.

Store in a cool, dry, well-ventilated location.
Inside storage should be in a standard flammable liquids storage warehouse, room, or cabinet.

Separate from oxidizing material and other reactive hazards.
Store bulk quantities in detached tanks provided with refrigeration and inert gas cover.

Acetaldehyde is recommended that steel storage tanks of suitable std be used.
Storage vessels should be fitted with temp gauges & automatic water sprays.

All tanks & equipment must be earthed.
Transfer of material by pipeline must be by pressure of nitrogen.
Drums containing acetaldehyde should never be stored in direct sunlight or other warm areas.

Reactivity Profile of Acetaldehyde:
Acetaldehyde undergoes a vigorously exothermic condensation reaction in contact with strong acids, bases or traces of metals.
Can react vigorously with oxidizing reagents such as dinitrogen pentaoxide, hydrogen peroxide, oxygen, silver nitrate, etc.
Contamination often leads either to reaction with the contaminant or polymerization, both with the evolution of heat.

Can react violently with acid anhydrides, alcohols, ketones, phenols, ammonia, hydrogen cyanide, hydrogen sulfide, halogens, phosphorus, isocyanates, concentrated sulfuric acid, and aliphatic amines.
Reactions with cobalt chloride, mercury(II) chlorate or perchlorate form sensitive, explosive products.

An oxygenation reaction of Acetaldehyde in the presence of cobalt acetate at -20°C exploded violently when stirred.
The event was ascribed to peroxyacetate formation.

Safety Profile of Acetaldehyde:
Acetaldehyde is confirmed carcinogen with experimental carcinogenic and tumorigenic data.
Poison by intratracheal and intravenous routes.

Acetaldehyde is human systemic irritant by inhalation.
Acetaldehyde is human systemic irritant by inhalation.
Acetaldehyde is a experimental teratogen.

Acetaldehyde has other experimental reproductive effects.
Acetaldehyde is skin and severe eye irritant.

Acetaldehyde is a narcotic.
Acetaldehyde is common air contaminant.

Acetaldehyde is highly flammable liquid.
Acetaldehyde mixtures of 30-60% of the vapor in air ignite above 100℃.

Acetaldehyde can react violently with acid anhydrides, alcohols, ketones, phenols, NH3, HCN, H2S, halogens, P, isocyanates, strong alkalies, and amines.

Reactions with cobalt chloride, mercury(Ⅱ) chlorate, or mercury(Ⅱ) perchlorate form violently in the presence of traces of metals or acids.
Reaction with oxygen may lead to detonation.
When heated to decomposition Acetaldehyde emits acrid smoke and fumes.

Health Effects of Acetaldehyde:
Health effects of exposure to acetaldehyde have been examined in toxicological and controlled human exposure studies, with very little epidemiological evidence related to indoor acetaldehyde exposure.
In this assessment, the short-term exposure limit is derived from the results of a controlled human exposure study, whereas the long-term exposure limit is based on toxicological data from a study in a rodent model.
Supporting evidence is provided by the results of other toxicological and controlled human exposure studies.

Based on the evidence from human and toxicological studies, the effects of short-term and long-term acetaldehyde inhalation are observed at the site of entry.
Key health effects include tissue damage and cancer development, mainly in the upper respiratory tract.

First Aid Measures of Acetaldehyde:

EYES:
First check the victim for contact lenses and remove if present.
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.

Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

SKIN:
IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing.
Gently wash all affected skin areas thoroughly with soap and water.

IMMEDIATELY call a hospital or poison control center even if no symptoms (such as redness or irritation) develop.
IMMEDIATELY transport the victim to a hospital for treatment after washing the affected areas.

INHALATION:
IMMEDIATELY leave the contaminated area; take deep breaths of fresh air.
IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop.

Provide proper respiratory protection to rescuers entering an unknown atmosphere.
Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.

INGESTION:
DO NOT INDUCE VOMITING.
Volatile chemicals have a high risk of being aspirated into the victim's lungs during vomiting which increases the medical problems.

If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center.
IMMEDIATELY transport the victim to a hospital.

If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body.
DO NOT INDUCE VOMITING.
IMMEDIATELY transport the victim to a hospital.

Since this chemical is a known or suspected carcinogen you should contact a physician for advice regarding the possible long term health effects and potential recommendation for medical monitoring.
Recommendations from the physician will depend upon the specific compound, Acetaldehyde chemical, physical and toxicity properties, the exposure level, length of exposure, and the route of exposure.

Fire Fighting of Acetaldehyde:

All these products have a very low flash point:
Use of water spray when fighting fire may be inefficient.

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.
Do not use dry chemical extinguishers to control fires involving nitromethane (UN1261) or nitroethane (UN2842).

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Do not use straight streams.
Move containers from fire area if you can do Acetaldehyde without risk.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.
For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn.

Isolation and Evacuation of Acetaldehyde:
As an immediate precautionary measure, isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Spillage Disposal of Acetaldehyde:
Remove all ignition sources.

Evacuate danger area! Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of the Acetaldehyde.
Do NOT let this chemical enter the environment.
Collect leaking liquid in sealable containers.

Absorb remaining liquid in sand or inert absorbent.
Then store and dispose of according to local regulations.

Do NOT absorb in saw-dust or other combustible absorbents.
Remove vapour with fine water spray.

Cleanup Methods of Acetaldehyde:

Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
Avoid breathing vapors, mist or gas.

Ensure adequate ventilation.
Remove all sources of ignition.
Evacuate personnel to safe areas.

Beware of vapors accumulating to form explosive concentrations.
Vapors can accumulate in low areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Contain spillage, and then collect with an electrically protected vacuum cleaner or by wet-brushing and place in container for disposal according to local regulations.

(1) Remove all ignition sources
(2) Ventilate area to disperse gas
(3) If in gaseous form, stop flow of gas
(4) If in liquid form, for small quantities absorb on paper towels.
Evaporate in safe place (fume hood).

Allow sufficient time for vapors to completely clear hood ductwork, then burn the paper in a location away from combustible materials.

Large quantities can be reclaimed or collected and atomized in a suitable combustion chamber.
Acetaldehyde should not be allowed to enter a confined space such as a sewer, because of possibility of an explosion.
Sewers designed to preclude the formation of explosive concentration of acetaldehyde vapors are permitted.

Identifiers of Acetaldehyde:
CAS Number: 75-07-0
ChEBI: CHEBI:15343
ChEMBL: ChEMBL170365
ChemSpider: 172
ECHA InfoCard: 100.000.761
EC Number: 200-836-8
IUPHAR/BPS: 6277
KEGG: C00084
PubChem CID: 177
RTECS number: AB1925000
UNII: GO1N1ZPR3B
CompTox Dashboard (EPA): DTXSID5039224
InChI:
InChI=1S/C2H4O/c1-2-3/h2H,1H3
Key: IKHGUXGNUITLKF-UHFFFAOYSA-N
InChI=1/C2H4O/c1-2-3/h2H,1H3
Key: IKHGUXGNUITLKF-UHFFFAOYAB
SMILES:
O=CC
CC=O

Properties of Acetaldehyde:
Chemical formula: C2H4O
Molar mass: 44.053 g·mol−1
Appearance: Colourless gas or liquid
Odor: Ethereal
Density:
0.784 g·cm−3 (20 °C)
0.7904–0.7928 g·cm−3 (10 °C)
Melting point: −123.37 °C (−190.07 °F; 149.78 K)
Boiling point: 20.2 °C (68.4 °F; 293.3 K)
Solubility in water: miscible
Solubility: miscible with ethanol, ether, benzene, toluene, xylene, turpentine, acetone
slightly soluble in chloroform
log P: -0.34
Vapor pressure: 740 mmHg (20 °C)
Acidity (pKa): 13.57 (25 °C, H2O)
Magnetic susceptibility (χ): -.5153−6 cm3/g
Refractive index (nD): 1.3316
Viscosity: 0.21 mPa-s at 20 °C (0.253 mPa-s at 9.5 °C)

Molecular Weight: 44.05
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 44.026214747
Monoisotopic Mass: 44.026214747
Topological Polar Surface Area: 17.1 Ų
Heavy Atom Count: 3
Complexity: 10.3
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Quality Level: 400
grade:
FG
Halal
Kosher
natural
reg. compliance:
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
vapor density: 1.52 (vs air)
vapor pressure: 14.63 psi ( 20 °C)
assay: ≥99% (GC)
form: liquid
autoignition temp.: 365 °F
expl. lim.: 60 %
refractive index: n20/D 1.332 (lit.)
pH: 5 (20 °C)
bp: 21 °C (lit.)
mp: −125 °C (lit.)
density: 0.785 g/mL at 25 °C (lit.)
application(s): flavors and fragrances
Documentation: see Safety & Documentation for available documents
food allergen: no known allergens
Organoleptic: ethereal
storage temp.: 2-8°C
SMILES string: CC=O
InChI: 1S/C2H4O/c1-2-3/h2H,1H3
InChI key: IKHGUXGNUITLKF-UHFFFAOYSA-N

Boiling point: 20.4 °C (1013 hPa)
Density: 0.78 g/cm3 (20 °C)
Explosion limit: 4 - 57 %(V)
Flash point: -38.89 °C
Ignition temperature: 140 °C
Melting Point: -123.5 °C
pH value: 5 (H₂O, 20 °C)
Vapor pressure: 1202 hPa (25 °C)

Structure of Acetaldehyde:
Molecular shape:
trigonal planar (sp2) at C1
tetrahedral (sp3) at C2
Dipole moment: 2.7 D

Thermochemistry of Acetaldehyde:
Heat capacity (C) of Acetaldehyde:: 89 J·mol−1·K−1
Std molar entropy (So298): 160.2 J·mol−1·K−1
Std enthalpy of formation (ΔfH⦵298): −192.2 kJ·mol−1
Gibbs free energy (ΔfG˚): -127.6 kJ·mol−1

Names of Acetaldehyde:

Preferred IUPAC name:
Acetaldehyde

Systematic IUPAC name:
Ethanal

Other names:
Acetic aldehyde
Ethyl aldehyde
Acetylaldehyde
ACETAMIDE
Acetamide, also known as ethanamid or acetic acid amide, belongs to the class of organic compounds known as carboximidic acids.
These are organic acids with the general formula RC(=N)-OH.
Acetamide is soluble in water and low molecular mass alcohols.

CAS Number: 60-35-5
EC Number: 200-473-5
Chemical Formula: CH3CONH2
Molar Mass: 59.07 g/mol

Acetamide is a colorless, crystalline (sand-like) material.
Acetamide is used in lacquers, explosives, and soldering flux, and as a stabilizer, plasticizer and solvent.

Acetamide forms deliquescent hexagonal crystals that are odorless when pure, but Acetamide frequently has a mousy odor.

Pure acetamide has a bitter taste.
Acetamide is used as a solvent and as a plasticizer.

Acetamide has been classified by the International Agency for Research on Cancer (IARC) as a Group 2B possible human carcinogen.
However, further studies need to be conducted to better understand the potential in vivo genotoxicity of acetamide.

Acetamide has also been investigated as a residue from some pesticides and as an impurity in the manufacture of pharmaceuticals.
Acetamide has been identified in milk, eggs, and meat.

Acetamide, also known as acetic acid or ethanamide, is a kind of inorganic chemical.
Furthermore, because the simplest amide is formed from acetic acid, Acetamide is slightly acidic in nature.

Acetamide applications include industrial solvents and plasticizers.
Acetamide also has a higher pH value than acetone on a pH scale.

Ethanamide is a colorless chemical with a mousy odor that is formed as a hygroscopic solid.
Acetamide is highly soluble in chloroform, water, glycerol, and hot benzene, and is mildly soluble in ether.

Acetamide belongs to the acetamides class and is formed via the formal condensation of acetic acid (CH3COOH) with ammonia (NH3).
Acetamide is naturally present in red beetroot.

Acetamide is used as an industrial solvent, plasticizer, wetting and penetrating agent.
Acetamide is also used for the transamidation of carboxamides in 1,4-dioxane.

Acetamide finds application in lacquers and soldering flux.
Further, Acetamide acts as a precursor to thioacetamide.

Acetamide, also known as ethanamid or acetic acid amide, belongs to the class of organic compounds known as carboximidic acids.
These are organic acids with the general formula RC(=N)-OH (R=H, organic group).

Acetamide is formally rated as a possible carcinogen (by IARC 2B) and is also a potentially toxic compound.
Based on a literature review a significant number of articles have been published on Acetamide.

Acetamide is also called Acetic acid amide, or Ethanamide or Acetimidic acid.
Acetamide is derived from acetic acid and is the simplest amide.
Acetamide is widely used as a plasticizer.

Ethanamide is obtained as a hygroscopic solid which is colourless and has a mousy odour.
Acetamide is readily soluble in water, chloroform, hot benzene, glycerol and slightly soluble in ether.

Acetamide is a member of the class of acetamides which results from the formal condensation of acetic acid (CH3COOH) with ammonia (NH3).
Acetamide is naturally found in red beetroot.

Acetamide (systematic name: ethanamide) is an organic compound with the formula CH3CONH2.
Acetamide is derived from acetic acid.

Acetamide finds some use as a plasticizer and as an industrial solvent.
The related compound N,N-dimethylacetamide (DMA) is more widely used, but Acetamide is not prepared from acetamide.

Acetamide can be considered an intermediate between acetone, which has two methyl (CH3) groups either side of the carbonyl (CO), and urea which has two amide (NH2) groups in those locations.
Acetamide is also a naturally occurring mineral with the IMA symbol: Ace.

Applications of Acetamide:
Acetamide was used as a supplement for growth media and for complementation of tlyA transposon mutants.
Acetamide was used as a component for cryoprotectant solution to study the ultrastructural changes in bovine oocytes by using vitrification.

Acetamide is used as an industrial solvent, plasticizer, wetting and penetrating agent.
Acetamide is also used for the transamidation of carboxamides in 1,4-dioxane.

Acetamide finds application in lacquers and soldering flux.
Further, Acetamide acts as a precursor to thioacetamide.

Uses of Acetamide:
Mainly, Acetamide is used as a solvent for many inorganic and organic compounds and in explosives.
Furthermore, industries use Acetamide as a plasticizer and hygroscopic agent.
Also, they use Acetamide to manufacture methylamine and as a stabilizer.

Besides, Acetamide can act as a penetrating agent and fire suppressant.

Acetamide is used as a solvent for many inorganic and organic compounds.
Acetamide is used in explosives.

Acetamide is used as a plasticizer.
Acetamide is used as a hygroscopic agent.

Acetamide is used to manufacture methylamine.
Acetamide is used as a stabilizer.

Acetamide is used as a penetrating agent.
Acetamide is used as a fire suppressant.

Acetamide is used as a plasticizer and an industrial solvent.
Molten acetamide is good solvent with a broad range of applicability.

Notably, Acetamide dielectric constant is higher than most organic solvents, allowing Acetamide to dissolve inorganic compounds with solubilities closely analogous to that of water.
Acetamide has uses in electrochemistry and the organic synthesis of pharmaceuticals, pesticides, and antioxidants for plastics.

Acetamide is a precursor to thioacetamide.
Acetamide is used as a solvent, plasticizer, and a wetting and penetrating agent.

Acetamide is used as a solvent, plasticizer, stabilizer, humectant for paper, hygroscopic agent, wetting agent, penetrating agent, and denaturant of alcohol.
Also used in lacquers, explosives, and soldering fluxes.

Acetamide is used as a solvent in the following applications: plasticizers, lacquers, explosives, soldering flux, wetting agents, and synthesis of other agents.
Acetamide is organic synthesis (reactant, solvent, peroxide stabilizer), general solvent, lacquers, explosives, soldering flux, hygroscopic agent, wetting agent, penetrating agent.

Acetamide suppresses acid buildup in printing inks, lacquers, explosives, and perfumes.
Acetamide is a mild moisturizer and is used as a softener for leather, textiles, paper, and certain plastics.

Acetamide and substituted acetamide-containing thiourea can be used for treatment of herpes viruses.
Derivatives can also be used as feeding behavior modifiers.

This is an endogenously produced metabolite found in the human body.
Acetamide is used in metabolic reactions, catabolic reactions or waste generation.

Solvent:
Acetamide is an excellent solvent for many organic and inorganic compounds.

Solubilizer:
Acetamide is renders sparingly soluble substances more soluble in water by mere addition or by fusion.

Other Uses of Acetamide:
Soldering
Pulp and Paper Processing
Painting (Solvents)

Workplace Controls and Practices of Acetamide:
Very toxic chemicals, or those that are reproductive hazards or sensitizers, require expert advice on control measures if a less toxic chemical cannot be substituted.

Control measures include:
Enclosing chemical processes for severely irritating and corrosive chemicals, using local exhaust ventilation for chemicals that may be harmful with a single exposure, and using general ventilation to control exposures to skin and eye irritants.

The following work practices are also recommended:
Label process containers.
Provide employees with hazard information and training.

Monitor airborne chemical concentrations.
Use engineering controls if concentrations exceed recommended exposure levels.

Provide eye wash fountains and emergency showers.
Wash or shower if skin comes in contact with a hazardous material.

Always wash at the end of the workshift.
Change into clean clothing if clothing becomes contaminated.

Do not take contaminated clothing home.
Get special training to wash contaminated clothing.

Do not eat, smoke, or drink in areas where chemicals are being handled, processed or stored.
Wash hands carefully before eating, smoking, drinking, applying cosmetics or using the toilet.

In addition, the following may be useful or required:
Use a vacuum or a wet method to reduce dust during cleanup.
DO NOT DRY SWEEP.

Formula and Structure of Acetamide:
The chemical formula of acetamide is C2H5NO or CH3CONH2.
Moreover, Acetamide molar mass is 59.07 g/mol.

The acetamide has a methyl group (-CH3) bound to a carbonyl (CO) and Amine (NH2).
Besides, the acetamide primarily comprises of carboxylic acid amide functional group that has a general structure RC (=O) NH2.

Furthermore, the acetamide belongs to the family of primary carboxylic acid amides.
Also, Acetamide exists in nature as a natural compound.

The Acetamide chemical formula is CH3CONH2 or C2H5NO.
Acetamide has a molar mass of 59.07 g/mol as well.

Acetamide has a methyl group (-CH3) that is bonded to an amine (NH2) and a carbonyl group (CO).
On the other hand, Acetamide is predominantly composed of a carboxylic acid amide functional group with a conventional structure of RC (=O) NH2.

Similarly, Acetamide is a member of the family of primary carboxylic acid amides.
Also, Acetamide exists in nature and can be discovered as a natural compound.

Occurrence of Acetamide:
Acetamide has been detected near the center of the Milky Way galaxy.
This finding is potentially significant because acetamide has an amide bond, similar to the essential bond between amino acids in proteins.
This finding lends support to the theory that organic molecules that can lead to life (as we know Acetamide on Earth) can form in space.

On 30 July 2015, scientists reported that upon the first touchdown of the Philae lander on comet 67/P's surface, measurements by the COSAC and Ptolemy instruments revealed sixteen organic compounds, four of which – acetamide, acetone, methyl isocyanate, and propionaldehyde – were seen for the first time on a comet.
In addition, acetamide is found infrequently on burning coal dumps, as a mineral of the same name.

Generally, the acetamide occurs in burning waste coal piles that form between 50 and 150oC (122-302oF).
Also, Acetamide only appears in periods of dry weather.

Furthermore, the scientist has detected Acetamide presence near the center of the Milky Way galaxy.
Also, this finding is potentially significant for amino acids in proteins.
Moreover, this finding lends support to the theory that organic molecules that can lend to life can form in space.

Production of Acetamide:
In chemical laboratories, Acetamide can be produced by dehydration of ammonium acetate.

The reaction is as follows:
[NH4][CH3CO2] → CH3C(O)NH2 + H2O

Acetamide can also be obtained through ammonolysis of acetylacetone with the under conditions that are used in reductive amination.
Alternately, Acetamide can be produced from anhydrous acetic acid (CH3COOH), dried hydrogen chloride gas, and acetonitrile in an ice bath along with a reagent acetyl chloride.

On an industrial scale, Acetamide can be produced by dehydrating ammonium acetate or by hydrolyzing acetonitrile.
CH3CN + H2O → CH3C(O)NH2

Laboratory scale:
Acetamide can be produced in the laboratory from ammonium acetate by dehydration:
[NH4][CH3CO2] → CH3C(O)NH2 + H2O

Alternatively acetamide can be obtained in excellent yield via ammonolysis of acetylacetone under conditions commonly used in reductive amination.
Acetamide can also be made from anhydrous acetic acid, acetonitrile and very well dried hydrogen chloride gas, using an ice bath, alongside more valuable reagent acetyl chloride.
Yield is typically low (up to 35%), and the acetamide made this way is generated as a salt with HCl.

Industrial scale:
In a similar fashion to some laboratory methods, acetamide is produced by dehydrating ammonium acetate or via the hydration of acetonitrile, a byproduct of the production of acrylonitrile:
CH3CN + H2O → CH3C(O)NH2

Physical Properties of Acetamide:
We can identify Acetamide in the field as transparent to translucent, colorless or gray variations.
Also, it has a white streak.

The density of acetamide is 1.17 g/cm3 and hardness of 1 to 1.5 roughly close to talc or a slightly harder substance.
The melting point of acetamide is between 79 to 81oC, whereas Acetamide boiling point is 221.2oC.

Furthermore, Acetamide density is 1.159 g/cm3.
Besides, Acetamide is soluble in water (2000 g L-1), ethanol (500 g L-1), pyridine (166.67 g L-1), chloroform, glycerol, hot benzene, slightly soluble in ether.

Chemical Properties of Acetamide:
We find Acetamide as hygroscopic solid that is colorless and has a mousy odor which depends on Acetamide purity.
Also, Acetamide has a bitter taste.

Furthermore, Acetamide is a member of the class of acetamides which results from the formal condensation of acetic acid (CH3COOH) with ammonia (NH3).
Most importantly, the carbonyl, methyl and anime groups share electrons with each other to form acetamide.

Handling and Storage of Acetamide:
Prior to working with Acetamide you should be trained on Acetamide proper handling and storage.

Acetamide reacts with oxidizing agents (such as perchlorates, peroxides, permanganates, chlorates, nitrates, chlorine, bromine and fluorine).
Strong acids (such as hydrochloric, sulfuric and nitric).
Strong bases (such as sodium hydroxide and potassium hydroxide) and reducing agents.

Store in tightly closed containers in a cool, well-ventilated area.

First Aid Measures of Acetamide:

EYES:
First check the victim for contact lenses and remove if present.
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.

Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

SKIN:
IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing.
Gently wash all affected skin areas thoroughly with soap and water.
If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.

INHALATION:
IMMEDIATELY leave the contaminated area.
Take deep breaths of fresh air.

IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop.
Provide proper respiratory protection to rescuers entering an unknown atmosphere.

Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used.
If not available, use a level of protection greater than or equal to that advised under Protective Clothing.

INGESTION:
DO NOT INDUCE VOMITING.
If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center.

Be prepared to transport the victim to a hospital if advised by a physician.
If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body.

DO NOT INDUCE VOMITING.
IMMEDIATELY transport the victim to a hospital.

OTHER:
Since this chemical is a known or suspected carcinogen you should contact a physician for advice regarding the possible long term health effects and potential recommendation for medical monitoring.
Recommendations from the physician will depend upon the specific compound, Acetamide, physical and toxicity properties, the exposure level, length of exposure, and the route of exposure.

Fire Fighting of Acetamide:

Fire Fighting Procedures:

Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical, or carbon dioxide.

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Use dry chemical, carbon dioxide, water spray, or alcohol foam extinguishers.

If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters.
Notify local health and fire officials and pollution control agencies.

From a secure, explosion-proof location, use water spray to cool exposed containers.
If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position.

The only respirators recommended for firefighting are self-contained breathing apparatuses that have full face-pieces and are operated in a pressure-demand or other positive-pressure mode.

Accidental Release Measures of Acetamide:

Spillage Disposal:

Personal protection:
P2 filter respirator for harmful particles.
Sweep spilled substance into covered containers.

If appropriate, moisten first to prevent dusting.
Carefully collect remainder.
Then store and dispose of according to local regulations.

Cleanup Methods of Acetamide:

Accidental Release Measures:

Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.

Avoid dust formation.
Avoid breathing vapors, mist or gas.

Ensure adequate ventilation.
Evacuate personnel to safe areas.
Avoid breathing dust.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let Acetamide enter drains.

Methods and materials for containment and cleaning up:
Pick up and arrange disposal without creating dust.
Sweep up and shovel.

Keep in suitable, closed containers for disposal.
Evacuate persons not wearing protective equipment from area of spill or leak until cleanup is complete.

Remove all ignition sources.
Collect powdered material in the most convenient and safe manner and deposit in sealed containers. Ventilate area after cleanup is complete.

Material is very water soluble and hydrolyzes slowly to ammonia and acetate salts.
May be removed from alkaline solutions with adsorbent carbon.

Acetamide may be necessary to contain and dispose of this chemical as a hazardous waste.
If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters.

PRECAUTIONS FOR "CARCINOGENS":
A high-efficiency particulate arrestor (HEPA) or charcoal filters can be used to minimize amt of carcinogen in exhausted air ventilated safety cabinets, lab hoods, glove boxes or animal rooms.
Filter housing that is designed so that used filters can be transferred into plastic bag without contaminating maintenance staff is avail commercially.

Filters should be placed in plastic bags immediately after removal.
The plastic bag should be sealed immediately.

The sealed bag should be labelled properly.
Waste liquids should be placed or collected in proper containers for disposal.

The lid should be secured & the bottles properly labelled.
Once filled, bottles should be placed in plastic bag, so that outer surface is not contaminated.

The plastic bag should also be sealed & labelled.
Broken glassware should be decontaminated by solvent extraction, by chemical destruction, or in specially designed incinerators.

Identifiers of Acetamide:
CAS Number: 60-35-5
ChEBI: CHEBI:27856
ChEMBL: ChEMBL16081
ChemSpider: 173
DrugBank: DB02736
ECHA InfoCard: 100.000.430
EC Number: 200-473-5
IUPHAR/BPS: 4661
KEGG: C06244
PubChem CID: 178
RTECS number: AB4025000
UNII: 8XOE1JSO29 check
CompTox Dashboard (EPA): DTXSID7020005
InChI:
InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
Key: DLFVBJFMPXGRIB-UHFFFAOYSA-N
InChI=1/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
Key: DLFVBJFMPXGRIB-UHFFFAOYAC
SMILES: O=C(N)C

CAS number: 60-35-5
EC index number: 616-022-00-4
EC number: 200-473-5
Hill Formula: C₂H₅NO
Chemical formula: CH₃CONH₂
Molar Mass: 59.07 g/mol
HS Code: 2924 19 00

Properties of Acetamide:
Chemical formula: C2H5NO
Molar mass: 59.068 g·mol−1
Appearance: colorless, hygroscopic solid
Odor: odorless
mouse-like with impurities
Density: 1.159 g cm−3
Melting point: 79 to 81 °C (174 to 178 °F; 352 to 354 K)
Boiling point: 221.2 °C (430.2 °F; 494.3 K) (decomposes)
Solubility in water: 2000 g L−1
Solubility: ethanol 500 g L−1
pyridine 166.67 g L−1
soluble in chloroform, glycerol, benzene
log P: −1.26
Vapor pressure: 1.3 Pa
Acidity (pKa): 15.1 (25 °C, H2O)
Magnetic susceptibility (χ): −0.577 × 10−6 cm3 g−1
Refractive index (nD): 1.4274
Viscosity: 2.052 cP (91 °C)

Boiling point: 221 - 222 °C (1013 hPa)
Density: 1.159 g/cm3
Melting Point: 78 - 81 °C
Vapor pressure: 1.61 hPa (20 °C)
Solubility: 2200 g/l

C2H5NO: Acetamide
Molecular weight/molar mass of C2H5NO: 59.068 g/mol
Density of Acetamide: 1.159 g/cm3
Boiling Point of Acetamide: 221.2 °C
Melting Point of Acetamide: 79 to 81 °C

Vapor pressure: 1 mmHg ( 65 °C)
Quality Level: 200
Assay: ≥99.0% (GC)
Form: crystals
bp: 221 °C (lit.)

mp:
78-80 °C (lit.)
78-82 °C

Solubility:
H2O: soluble 1 gm in 0.5 ml
Alcohol: soluble 1 gm in 2ml
Pyridine: soluble 1 gm in 6 ml
Chloroform: soluble
Glycerol: soluble

SMILES string: CC(N)=O
InChI: 1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
InChI key: DLFVBJFMPXGRIB-UHFFFAOYSA-N

Molecular Weight: 59.07
XLogP3-AA: -0.9
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 59.037113783
Monoisotopic Mass: 59.037113783
Topological Polar Surface Area: 43.1 Ų
Heavy Atom Count: 4
Complexity: 33
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Structure of Acetamide:
Crystal structure: trigonal

Thermochemistry of Acetamide:
Heat capacity (C): 91.3 J·mol−1·K−1
Std molar entropy (S⦵298): 115.0 J·mol−1·K−1
Std enthalpy of formation (ΔfH⦵298): −317.0 kJ·mol−1

Specifications of Acetamide:
Assay (GC, area%): ≥ 99.0 % (a/a)
Melting range (lower value): ≥ 77 °C
Melting range (upper value): ≤ 80 °C

Melting Point: 76°C to 81°C
Density: 1.159
Boiling Point: 220°C to 222°C
Beilstein: 1071207
Merck Index: 14,43
Quantity: 1000 g
Solubility Information: Soluble in water.
Sensitivity: Hygroscopic
Formula Weight: 59.07
Percent Purity: 99%
Chemical Name or Material: Acetamide

Names of Acetamide:

Preferred IUPAC name:
Acetamide

Systematic IUPAC name:
Ethanamide

Other names:
Acetic acid amide
Acetylamine

Synonyms of Acetamide:
Acetamid
Acetamide, monosodium salt
Acetate amide
Acetic acid amide
Acetimidic acid
ACM
Amid kyseliny octove
Azetamid
CH3CONH2
Essigsaeureamid
Ethanamid
Ethanamide
Methanecarboxamide
acetamide
60-35-5
Ethanamide
Acetic acid amide
Methanecarboxamide
Acetimidic acid
Ethanimidic acid
Amide C2
Amid kyseliny octove
Caswell No. 003H
Acetimidic acid (VAN)
CCRIS 2
NCI-C02108
HSDB 4006
CH3CONH2
AI3-02060
8XOE1JSO29
CHEBI:27856
NSC-25945
acetamid
74330-92-0
acetoamide
Ethanamid
Amid kyseliny octove [Czech]
EINECS 200-473-5
NSC 25945
UNII-8XOE1JSO29
acetylamine
BRN 1071207
Essigsaeureamid
imidoacetic acid
N-Methylformamde
MFCD00008023
Acetamide, >=98%
ACETAMIDE [MI]
ACETAMIDE [FHFI]
ACETAMIDE [HSDB]
ACETAMIDE [IARC]
ACETAMIDE, REAGENT
Lopac-A-0500
bmse000825
bmse000895
EC 200-473-5
ACETAMIDE [WHO-DD]
Acetamide, sublimed, 99%
WLN: ZV1
Acetic acid amide;Ethanamide
Acetamide, ~99% (GC)
Lopac0_000003
4-02-00-00399 (Beilstein Handbook Reference)
MLS002153504
Acetamide, analytical standard
BIDD:ER0566
CHEMBL16081
GTPL4661
DTXSID7020005
FEMA NO. 4251
Acetamide, crystalline, >=99%
CHEBI:49028
Acetamide, >=98.0% (GC)
Acetamide, >=99.0% (GC)
HMS3260A07
Acetamide (6CI,7CI,8CI,9CI)
BCP26153
HY-Y0946
NSC25945
STR01066
ZINC8034818
Tox21_300776
Tox21_500003
s6011
STL283915
AKOS000118788
AKOS015917387
CCG-204099
DB02736
LP00003
SDCCGSBI-0049992.P002
CAS-60-35-5
Benzeneacetic?acid,?|A-amino-4-methyl-
NCGC00015030-01
NCGC00015030-02
NCGC00015030-03
NCGC00015030-04
NCGC00015030-05
NCGC00015030-06
NCGC00093530-01
NCGC00093530-02
NCGC00254680-01
NCGC00260688-01
SMR000326670
A0007
CS-0015934
EU-0100003
FT-0603458
FT-0621721
FT-0621725
FT-0625737
EN300-15608
A 0500
C06244
A832706
Q421721
SR-01000076247
J-523678
SR-01000076247-1
Acetamide, zone-refined, purified by sublimation, 99%
Z33546370
F1908-0077
02U
ACETIC ACID
Acetic acid is an organic acid available in various standard strengths.
Pure acetic acid is known as Acetic Acid Glacial because it will freeze at moderate temperatures (16.6C).


CAS Number: 64-19-7
EC Number: 200-580-7
E number: E260 (preservatives)
Molecular Formula: C2H4O2 / CH3COOH



SYNONYMS:
Acetic acid, Ethanoic acid, Vinegar (when dilute), Hydrogen acetate, Methanecarboxylic acid, Ethylic acid, Ethanoic acid, Ethylic acid, Glacial acetic acid, Methanecarboxylic acid, Vinegar acid, CH3COOH, Acetasol, Acide acetique, Acido acetico, Azijnzuur, Essigsaeure, Octowy kwas, Acetic acid, glacial, Kyselina octova, UN 2789, Aci-jel, Shotgun, Ethanoic acid monomer, NSC 132953, Ethanoic acid, vinegar, ethylic acid, vinegar acid, methanecarboxylic acid, TCLP extraction fluid 2, shotgun, glacial acetic acid, glacial ethanoic acid, Ethanoic acid, Ethylic acid, Glacial acetic acid, Methanecarboxylic acid, Vinegar acid, CH3COOH, Acetasol, Acide acetique, Acido acetico, Azijnzuur, Essigsaeure, Octowy kwas, Acetic acid, glacial, Kyselina octova, UN 2789, Aci-jel, Shotgun, Ethanoic acid monomer, NSC 132953, BDBM50074329, FA 2:0, LMFA01010002, NSC132953, NSC406306, Acetic acid for HPLC >=99.8%, AKOS000268789, ACIDUM ACETICUM [WHO-IP LATIN], DB03166, UN 2789, Acetic acid >=99.5% FCC FG, Acetic acid natural >=99.5% FG, Acetic acid ReagentPlus(R) >=99%, CAS-64-19-7, USEPA/OPP Pesticide Code: 044001, Acetic acid USP 99.5-100.5%, NCGC00255303-01, Acetic acid 1000 microg/mL in Methanol, Acetic acid SAJ first grade >=99.0%, Acetic acid 1000 microg/mL in Acetonitrile, Acetic acid >=99.99% trace metals basis, Acetic acid JIS special grade >=99.7%, Acetic acid purified by double-distillation, NS00002089, Acetic acid UV HPLC spectroscopic 99.9%, EN300-18074, Acetic acid Vetec(TM) reagent grade >=99%, Bifido Selective Supplement B for microbiology, C00033, D00010, ORLEX HC COMPONENT ACETIC ACID GLACIAL, Q47512, VOSOL HC COMPONENT ACETIC ACID GLACIAL, Acetic acid glacial electronic grade 99.7%, TRIDESILON COMPONENT ACETIC ACID GLACIAL, A834671, ACETASOL HC COMPONENT ACETIC ACID GLACIAL, Acetic acid >=99.7% SAJ super special grade, ACETIC ACID GLACIAL COMPONENT OF BOROFAIR, ACETIC ACID GLACIAL COMPONENT OF ORLEX HC, ACETIC ACID GLACIAL COMPONENT OF VOSOL HC, SR-01000944354, ACETIC ACID GLACIAL COMPONENT OF TRIDESILON, SR-01000944354-1, ACETIC ACID GLACIAL COMPONENT OF ACETASOL HC, Glacial acetic acid meets USP testing specifications, InChI=1/C2H4O2/c1-2(3)4/h1H3(H,3,4), Acetic acid >=99.7% suitable for amino acid analysis, Acetic acid >=99.7% for titration in non-aqueous medium, Acetic acid for luminescence BioUltra >=99.5% GC, Acetic acid p.a. ACS reagent reag. ISO reag. Ph. Eur. 99.8%, Acetic acid semiconductor grade MOS PURANAL(TM) Honeywell 17926, Glacial acetic acid United States Pharmacopeia USP Reference Standard, Acetic acid puriss. p.a. ACS reagent reag. ISO reag. Ph. Eur. >=99.8%, Glacial Acetic Acid Pharmaceutical Secondary Standard Certified Reference Material, Acetic acid puriss. meets analytical specification of Ph. Eur. BP USP FCC 99.8-100.5%, acetic-acid, Glacial acetate, acetic cid, actic acid, UNII-Q40Q9N063P, acetic -acid, Distilled vinegar, Methanecarboxylate, Acetic acid glacial [USP:JAN], Acetasol (TN), Acetic acid glacial for LC-MS, Vinegar (Salt/Mix), HOOCCH3, 546-67-8, Acetic acid LC/MS Grade, ACETIC ACID [II], ACETIC ACID [MI], Acetic acid ACS reagent, bmse000191, bmse000817, bmse000857, Otic Domeboro (Salt/Mix), EC 200-580-7, Acetic acid (JP17/NF), ACETIC ACID [FHFI], ACETIC ACID [INCI], Acetic Acid [for LC-MS], ACETIC ACID [VANDF], NCIOpen2_000659, NCIOpen2_000682, Acetic acid glacial (USP), 4-02-00-00094 (Beilstein Handbook Reference), 77671-22-8, Glacial acetic acid (JP17), UN 2790 (Salt/Mix), ACETIC ACID [WHO-DD], ACETIC ACID [WHO-IP], ACETICUM ACIDUM [HPUS], GTPL1058, Acetic Acid Glacial HPLC Grade, Acetic acid analytical standard, Acetic acid Glacial USP grade, Acetic acid puriss. >=80%, Acetic acid 99.8% anhydrous, Acetic acid AR >=99.8%, Acetic acid LR >=99.5%, Acetic acid extra pure 99.8%, Acetic acid 99.5-100.0%, Acetic acid Glacial ACS Reagent, STR00276, Acetic acid puriss. 99-100%, Tox21_301453, Acetic acid glacial >=99.85%, acetic acid, ethanoic acid, 64-19-7, Ethylic acid, Vinegar acid, Acetic acid glacial, Glacial acetic acid, Acetic acid glacial, Methanecarboxylic acid, Acetasol, Essigsaeure, Acide acetique, Pyroligneous acid, Vinegar, Azijnzuur, Aceticum acidum, Acido acetico, Octowy kwas, Aci-jel, HOAc, ethoic acid, Kyselina octova, Orthoacetic acid, AcOH, Ethanoic acid monomer, Acetic, Caswell No. 003, Otic Tridesilon, MeCOOH, Acetic acid-17O2, Otic Domeboro, Acidum aceticum glaciale, Acidum aceticum, CH3-COOH, acetic acid-, CH3CO2H, UN2789, UN2790, EPA Pesticide Chemical Code 044001, NSC 132953, NSC-132953, NSC-406306, BRN 0506007, Acetic acid diluted, INS NO.260, Acetic acid [JAN], DTXSID5024394, MeCO2H, CHEBI:15366, AI3-02394, CH3COOH, INS-260, Q40Q9N063P, E-260, 10.Methanecarboxylic acid, CHEMBL539, NSC-111201, NSC-112209, NSC-115870, NSC-127175, Acetic acid-2-13C,d4, INS No. 260, DTXCID304394, E 260, Acetic-13C2 acid (8CI,9CI), Ethanoat, Shotgun, MFCD00036152, Acetic acid of a concentration of more than 10 per cent by weight of acetic acid, 285977-76-6, 68475-71-8, C2:0, acetyl alcohol, Orlex, Vosol, ACETIC-1-13C-2-D3 ACID-1 H (D), WLN: QV1, ACETIC ACID (MART.), ACETIC ACID [MART.], Acetic acid >=99.7%, 57745-60-5, 63459-47-2, FEMA Number 2006, ACETIC-13C2-2-D3 ACID, 97 ATOM % 13C, 97 ATOM % D, Acetic acid ACS reagent >=99.7%, ACY, HSDB 40, CCRIS 5952, 79562-15-5, methane carboxylic acid, EINECS 200-580-7, Acetic acid 0.25% in plastic container, Essigsaure, Ethylate, acetic acid



Acetic Acid is an organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).
Acetic Acid is a colourless liquid which when undiluted is also called ‘glacial acetic acid’.
Acetic acid is the main component of vinegar (apart from water; vinegar is roughly 8% acetic acid by volume), and has a distinctive sour taste and pungent smell.


Acetic Acid Food Grade is one of the simplest carboxylic acids.
Acetic Acid is an important chemical reagent and industrial chemical, mainly used in the production of cellulose acetate for photographic film and polyvinyl acetate for wood glue, as well as synthetic fibres and fabrics.


Acetic acid, also known as ethanoic acid, is a colourless liquid and organic compound.
With the chemical formula CH₃COOH, Acetic acid is a chemical reagent for the production of chemicals.
Acetic Acid has a CAS number of 64-19-7.


Acetic acid, CH3COOH, also known as ethanoic acid, is an organic acid which has a pungent smell.
Acetic Acid is a weak acid, in that it is only partially dissociated in an aqueous solution.
Acetic Acid is hygroscopic (absorbs moisture from the air) and freezes at 16.5C to a colourless crystalline solid.


Acetic acid is one of the simplest carboxylic acids, and is a very important industrial chemical.
Acetic Acid is produced by biological and synthetic ways in the industry.
The salt and Acetic Acid's ester are called acetate.


Acetic Acid is completely soluble in water.
Acetic acid is a chemical reagent for the production of chemicals.
The most common one-time use of acetic acid is for the production of vinyl acetate monomer as well as the production of acetic anhydride and esters.


The amount of acetic acid in vinegar is relatively small.
Acetic acid, otherwise known as ethanoic acid, is a simple carboxylic acid that usually forms a liquid at room temperature.
Acetic Acid is most widely used in table vinegar due to the preservative properties it holds and is the chemical responsible for the characteristic vinegar odour.


Acetic acid also has a wide range of applications in the chemical industry and is used in the synthesis of esters and vinyl acetate. Within a laboratory setting, acetic acid is a commonly used solvent.
Acetic Acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 000 tonnes per annum.


Acetic acid is a product of the oxidation of ethanol and of the destructive distillation of wood.
Acetic Acid is used locally, occasionally internally, as a counterirritant and also as a reagent.
Acetic acid otic (for the ear) is an antibiotic that treats infections caused by bacteria or fungus.


While this is usually the least expensive way of purchasing acetic acid we find that more dilute grades such as 90% are more in demand to eliminate most of the solidification problems.
Acetic acid may sound like it should be in a chemistry lab or science fair rather than in your kitchen pantry.


However, Acetic Acid is actually the main compound found in vinegar and is responsible for both its unique flavor and acidity.
Not only that, but Acetic Acid’s also believed to contribute to many of the health benefits of apple cider vinegar due to its potent medicinal properties.
Acetic acid, also known as ethanoic acid, is a chemical compound found in many different products.


Acetic Acid’s perhaps most well-known as the main component of vinegar, apart from water, and is thought to supply ingredients like apple cider vinegar with many of their health-promoting properties.
Chemically speaking, the acetic acid formula is C2H4O2, which can also be written as CH3COOH or CH3CO2H.


Because of the presence of a carbon atom in the acetic acid structure, it’s considered an organic compound.
The acetic acid density is about 1.05 grams/cm³; compared to other compounds like nitric acid, sulfuric acid or formic acid, the density of acetic acid is quite a bit lower.


Conversely, the acetic acid melting point is significantly higher than many other acids, and the acetic acid molar mass and acetic acid boiling point tend to fall right about in the middle.
Acetic acid which is also known as methane carboxylic acid and ethanoic acid is basically a clear, colorless liquid, which has a strong and pungent smell.


Since Acetic Acid has a carbon atom in its chemical formula, it is an organic compound and it comes with a chemical formula CH3COOH.
Interestingly, the word ‘acetic’ is derived from a Latin word called ‘acetum’ meaning ‘vinegar’.
Vinegar is the dilute form of acetic acid and is the most common chemical substance among people.


Acetic acid is a main component of vinegar and also gives vinegar its characteristic smell.
Acetic acid (CH3COOH), also called ethanoic acid, is the most important of the carboxylic acids.
A dilute (approximately 5 percent by volume) solution of acetic acid produced by fermentation and oxidation of natural carbohydrates is called vinegar; a salt, ester, or acylal of acetic acid is called acetate.


Moving on, when acetic acid or ethanoic acid is undiluted it is termed glacial acetic acid.
Acetic Acid is a weak acid but when it is in concentrated form, this acid is corrosive and can cause some damage to the skin.
Acetic Acid appears as a clear colorless liquid with a strong odor of vinegar.


Flash point of Acetic Acid is 104 °F.
Density of Acetic Acid is 8.8 lb / gal.
Acetic Acid is corrosive to metals and tissue.


Acetic acid, solution, more than 10% but not more than 80% acid appears as a colorless aqueous solution.
Acetic Acid smells like vinegar.
Acetic Acid is corrosive to metals and tissue.


Acetic acid, solution, more than 80% acid is a clear colorless aqueous solution with a pungent odor.
Acetic Acid is faintly pink wet crystals with an odor of vinegar.
Acetic acid is a simple monocarboxylic acid containing two carbons.


Acetic Acid has a role as a protic solvent, a food acidity regulator, an antimicrobial food preservative and a Daphnia magna metabolite.
Acetic Acid is a conjugate acid of an acetate.
Acetic acid is a product of the oxidation of ethanol and of the destructive distillation of wood.


Acetic acid is a metabolite found in or produced by Escherichia coli.
Acetic Acid is a natural product found in Camellia sinensis, Microchloropsis, and other organisms with data available.
Acetic Acid is a synthetic carboxylic acid with antibacterial and antifungal properties.


Although its mechanism of action is not fully known, undissociated acetic acid may enhance lipid solubility allowing increased fatty acid accumulation on the cell membrane or in other cell wall structures.
Acetic acid is one of the simplest carboxylic acids.


Acetic Acid is an important chemical reagent and industrial chemical that is used in the production of plastic soft drink bottles, photographic film; and polyvinyl acetate for wood glue, as well as many synthetic fibres and fabrics.
Acetic acid can be very corrosive, depending on the concentration.


Acetic Acid is one ingredient of cigarette.
The acetyl group, derived from acetic acid, is fundamental to the biochemistry of virtually all forms of life.
When bound to coenzyme A it is central to the metabolism of carbohydrates and fats.


However, the concentration of free acetic acid in cells is kept at a low level to avoid disrupting the control of the pH of the cell contents.
Acetic acid is produced and excreted by certain bacteria, notably the Acetobacter genus and Clostridium acetobutylicum.
These bacteria are found universally in foodstuffs, water, and soil, and acetic acid is produced naturally as fruits and some other foods spoil.


Acetic acid is also a component of the vaginal lubrication of humans and other primates, where it appears to serve as a mild antibacterial agent.
Acetic acid /əˈsiːtɪk/, systematically named ethanoic acid /ˌɛθəˈnoʊɪk/, is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH (also written as CH3CO2H, C2H4O2, or HC2H3O2).


Vinegar is at least 4% acetic acid by volume, making acetic acid the main component of vinegar apart from water.
Acetic Acid has been used, as a component of vinegar, throughout history from at least the third century BC.
Acetic acid is the second simplest carboxylic acid (after formic acid).


Acetic Acid is an important chemical reagent and industrial chemical across various fields, used primarily in the production of cellulose acetate for photographic film, polyvinyl acetate for wood glue, and synthetic fibres and fabrics.
Acetic Acid is a very important organic compound in the day-to-day lives of humans.


The desirable solvent properties of acetic acid, along with its ability to form miscible mixtures with both polar and non-polar compounds, make it a very important industrial solvent.
Acetic acid is also known as ethanoic acid, ethylic acid, vinegar acid, and methane carboxylic acid.


Acetic acid is a byproduct of fermentation, and gives vinegar its characteristic odor.
Vinegar is about 4-6% acetic acid in water.
More concentrated solutions can be found in laboratory use, and pure acetic acid containing only traces of water is known as glacial acetic acid.


Dilute solutions like vinegar can contact skin with no harm, but more concentrated solutions will burn the skin.
Glacial acetic acid can cause skin burns and permanent eye damage, and will corrode metal.
Acetic acid is an organic compound with the formula CH3COOH.


Acetic Acid is a carboxylic acid consisting of a methyl group that is attached to a carboxyl functional group.
The systematic IUPAC name of acetic acid is ethanoic acid and its chemical formula can also be written as C2H4O2.
Vinegar is a solution of acetic acid in water and contains between 5% to 20% ethanoic acid by volume.


The pungent smell and the sour taste are characteristic of the acetic acid present in it.
An undiluted solution of acetic acid is commonly referred to as glacial acetic acid.
Acetic Acid forms crystals which appear like ice at temperatures below 16.6oC.


Acetic acid (CH3COOH), the most important of the carboxylic acids.
A dilute (approximately 5 percent by volume) solution of acetic acid produced by fermentation and oxidation of natural carbohydrates is called vinegar; a salt, ester, or acylal of acetic acid is called acetate.


Industrially, acetic acid is used in the preparation of metal acetates, used in some printing processes; vinyl acetate, employed in the production of plastics; cellulose acetate, used in making photographic films and textiles; and volatile organic esters (such as ethyl and butyl acetates), widely used as solvents for resins, paints, and lacquers.


Biologically, acetic acid is an important metabolic intermediate, and it occurs naturally in body fluids and in plant juices.
Acetic acid has been prepared on an industrial scale by air oxidation of acetaldehyde, by oxidation of ethanol (ethyl alcohol), and by oxidation of butane and butene.


Today acetic acid is manufactured by a process developed by the chemical company Monsanto in the 1960s; it involves a rhodium-iodine catalyzed carbonylation of methanol (methyl alcohol).
Pure acetic acid, often called glacial acetic acid, is a corrosive, colourless liquid (boiling point 117.9 °C [244.2 °F]; melting point 16.6 °C [61.9 °F]) that is completely miscible with water.


Acetic acid is a clear, colorless, organic liquid with a pungent odor similar to household vinegar.
Acetic acid or glacial acetic acid, also known as ethanoic acid, is an organic compound with the chemical formula CH3COOH.
Pure glacial acetic acid (anhydrous acetic acid) is a colorless, hygroscopic liquid with a strong pungent odor.


The freezing point is 16.6°C, and Acetic Acid turns into colorless crystals after solidification.
Acetic Acid is an organic monobasic acid and can be miscible with water in any proportion.
Acetic Acid is particularly corrosive to metals.


Acetic acid is widely found in nature, such as in the fermentation metabolism and putrefaction products of various glacial acetic acid bacteria.
Acetic Acid is also the main component of vinegar.
Moreover, glacial acetic acid always plays an important role in many chemical reactions.


For example, Acetic Acid can undergo displacement reactions with metals such as iron, zinc, and copper to generate metal acetates and hydrogen.
In addition, Acetic Acid can react with alkalis, alkaline oxides, salts and certain metal oxides.
Acetic acid is an organic chemical substance, it is a colourless liquid with a very distinctive odour.


One of its most common uses is in the composition of vinegar, although Acetic Acid is also used in cosmetics and pharmaceuticals, in the food, textile and chemical industries.
On an industrial level, acetic acid is produced through the carbonylation of methanol and is used as a raw material for the production of different compounds.


Acetic Acid can also be obtained through the food industry by the acetic fermentation process of ethanol, or more commonly explained, through alcoholic fermentation and with the distillation of wood.
Pure acetic acid or glacial acetic acid, also known as CH3COOH, is a liquid that can be harmful to our health due to its irritating and corrosive properties and can cause severe skin, eye and digestive tract irritation.


However, thanks to its combination with different substances, Acetic Acid is possible to obtain everyday products that may be familiar to everyone, such as vinegar.
Vinegar is a hygroscopic substance, i.e. it can absorb moisture from its surroundings.


Therefore, when it is mixed with water, there is a very significant reduction in its volume.
On the other hand, when acetic acid 100 % is exposed to low temperatures, the surface, also known as acetic essence, crystallises and forms ice-like crystals at the top.


Due to the chemical structure of Acetic Acid, it has a very high boiling point.
Furthermore, it is worth noting that acetic acid, being a carboxylic acid, has the ability to dissociate, but only slightly, as it is a weak acid [FC1] .
Moreover, thanks to this ability to dissociate, Acetic Acid conducts electricity effectively.


Acetic Acid is an organic compound with the chemical formula CH3COOH.
Acetic Acid is an organic monobasic acid and is the main component of vinegar.
Pure anhydrous acetic acid (glacial acetic acid) is a colorless, hygroscopic liquid with a freezing point of 16.6 ℃ (62 ℉).


After solidification, Acetic Acid becomes a colorless crystal.
Acetic acid or ethanoic acid is a colourless liquid organic compound with the molecular formula CH3COOH.
When acetic acid is dissolved in water, it is termed glacial acetic acid.


Vinegar is no less than 4 per cent acetic acid by volume, aside from water, allowing acetic acid to be the main ingredient of vinegar.
Acetic Acid is produced primarily as a precursor to polyvinyl acetate and cellulose acetate, in addition to household vinegar.
Acetic Acid is a weak acid since the solution dissociates only slightly.


But concentrated acetic acid is corrosive and can damage the flesh.
The second simplest carboxylic acid is acetic acid (after formic acid).
Acetic Acid consists of a methyl group to which a carboxyl group is bound.


Acetic acid is a colourless liquid organic compound with pungent characteristic odour.
Acetic acid is an acid that occurs naturally.
Acetic acid can also be produced synthetically either by acetylene or by using methanol.


Acetic acid is considered as a natural preservative for food products.
Acetic acid has been used for hundreds of years as a preservative (vinegar, French for "sour wine").
If during the fermentation of grapes or other fruits, oxygen is allowed into the container, then bacteria convert the ethanol present into Acetic acid causing the wine to turn sour.


Acetic acid may be synthetically produced using methanol carbonylation, acetaldehyde oxidation, or butane/naphtha oxidation. Acetic acid is termed "glacial", and is completely miscible with water.
Acetic acid is the main component of vinegar.


Acetic acid appears as a clear, colorless liquid with a distinctive sour taste and pungent smell.
Acetic acid is used as a preservative, acidulant, and flavoring agent in mayonnaise and pickles.
Though Acetic acid’s considered safe, some are convinced it has potentially dangerous health effects.


Acetic acid systematically named ethanoic acid, is a colourless liquid organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).
When undiluted, Acetic acid is sometimes called glacial acetic acid.


Acetic acid is an organic compound belonging to the weak carboxylic acids.
The set of properties of Acetic acid classifies it as a broad-spectrum reagent and allows it to be used in a wide variety of industrial fields: from pharmacology and cosmetology to the chemical and food industries.


Acetic acid is one of the most common acids used in the food industry and household.
Acetic acid is a colorless, pungent, odorless liquid that miscible mixes with water to form solutions of varying concentrations.
Due to its ability to crystallize at an already positive temperature, Acetic acid is also known as “glacial”.


Acetic acid is a synthetic carboxylic acid with antibacterial and antifungal properties.
Although Acetic acid's mechanism of action is not fully known, undissociated acetic acid may enhance lipid solubility allowing increased fatty acid accumulation on the cell membrane or in other cell wall structures.


Acetic acid, as a weak acid, can inhibit carbohydrate metabolism resulting in subsequent death of the organism.
Acetic acid is present in most fruits.
Acetic acid is produced by bacterial fermentation and thus present in all fermented products.


In mayonnaise, Acetic acid is added to increase the inactivation of Salmonella.
Acetic acid, known also as ethanoic acid, is a weak acid that is commonly used as a food preservative and flavoring agent.
Acetic acid's chemical formula is CH3COOH, and its molecular weight is 60.05 g/mol.


Acetic acid is a clear, colorless liquid that has a pungent odor and a sour taste.
Acetic acid is miscible with water and most common organic solvents.
Acetic acid is produced naturally in most organisms as a byproduct of metabolism.


Acetic acid is also a major component of vinegar, which is a solution of acetic acid and water that occurs naturally when ethanol in fermented fruit juices undergoes oxidation by acetic acid bacteria.
The production of vinegar has been an ancient practice of food preservation and flavoring that dates back to ancient times.


Acetic acid has several applications outside of the food industry.
Acetic acid is used as a solvent in the production of various chemicals and is an important intermediate in the manufacture of polymers, fibers, and pharmaceuticals.


Acetic acid is classified as a weak acid because it only partially ionizes in water to produce hydrogen ions (H+) and acetate ions (CH3COO-).
The pH of a 1% solution of Acetic acid is approximately 2.4, which means it is acidic but relatively less acidic than some stronger acids like hydrochloric acid or sulfuric acid.


Acetic acid is both naturally occurring and synthetic.
Natural sources include fermentation and bacteria.
In fermentation, Acetic acid is produced when yeast breaks down sugar in the absence of oxygen.


Bacteria produce Acetic acid when they oxidize ethanol.
Synthetic Acetic acid is made by reacting methanol with carbon monoxide in the presence of a catalyst.
Acetic acid has a strong odor and taste.


The odor of Acetic acid is similar to that of vinegar and the taste is sour.
Acetic acid is not considered toxic in small quantities and is generally recognized as safe by the US Food and Drug Administration (FDA) when used in accordance with good manufacturing practices.


The safety of Acetic acid depends on its concentration, with higher concentrations being more corrosive to skin and eyes.
In summary, Acetic acid is a weak acid that is commonly used as a food preservative and flavoring agent.
Another important use of Acetic acid is as a chemical intermediate.


Lastly, Acetic acid is an important ingredient in the winemaking process.
In this case, Acetic acid is produced naturally as a byproduct of the wine fermentation process.
However, if Acetic acid levels are too high, it can cause a wine to taste or smell like vinegar, which is undesirable.


To avoid this, winemakers use sulfites to inhibit the growth of Acetic acid bacteria in the wine.
Acetic acid is also an effective cleaning agent, especially when it comes to eliminating stubborn stains or mineral build-up due to hard water.
Acetic acid's acidic nature helps to loosen dirt, grime, and other impurities from surfaces.


Acetic acid is found naturally in many foods, including vinegar and fermented products.
However, when used as an additive, Acetic acid is typically produced synthetically.
Acetic acid is generally recognized as safe (GRAS) when used in accordance with good manufacturing practices.


Overall, Acetic acid is considered a safe food additive when used within recommended limits.
As with any food additive, Acetic acid is essential to follow regulations and guidelines set by relevant authorities.



USES and APPLICATIONS of ACETIC ACID:
In the home, diluted acetic acid is often used in descaling agents.
In the food industry, acetic acid is used under the food additive (EU number E260) as an acidity regulator and as a condiment.
Acetic Acid is widely approved for usage as a food additive.


Acetic Acid 80% is an essential chemical with a wide range of applications.
Acetic Acid is a strong organic acid, also known as ethanoic or vinegar acid, and is used in a variety of industries, from the production of paints and adhesives to the food and pharmaceutical industries.


Acetic Acid is an efficient solvent and a condensing agent in chemical synthesis processes.
Acetic Acid is also used in the production of vinyl acetate, a key ingredient in polymer manufacturing.
Acetic Acid is a highly concentrated solution, ideal for professionals and experienced users.


With Acetic Acid you can remove stubborn limescale, green deposits and other types of pollution.
In general, for most applications Acetic Acid should first be diluted with water.
For a ready-made solution of acetic acid that you can use immediately for your cleaning work, you can also purchase cleaning vinegar .


Acetic Acid is most commonly used in the production of vinyl acetate monomer (VAM), in ester production and for the breeding of bees.
As a natural acid, acetic acid offers a wide range of possible applications: e.g. in cleaning formulations and for decalcification.
In addition, acetic acid is commonly used as a biogenic herbicide, although commercial use as a herbicide is not permitted on enclosed areas.


Applications of Acetic Acid: Adhesives/sealants-B&C, Agriculture intermediates, Apparel, Architectural coatings, Automotive protective coatings, Building materials, Commercial printing inks, Construction chemicals, Decorative interiors, Fertilizer, Food ingredients, Food preservatives, Formulators, Hard surface care, Industrial cleaners, Institutional cleaners, Intermediates, Oil or gas processing, Other-food chemicals, Other-transportation, Packaging components non-food contact, Paints & coatings, Pharmaceutical chemicals, Process additives, Refining, Specialty chemicals, Starting material, and Water treatment industrial.


Acetic Acid is a raw material used for the production of many downstream products.
For applications in drugs, foods, or feeds, Eastman provides acetic acid in grades appropriate for these regulated uses.
Acetic acid is most commonly found in vinegar, which is used in recipes ranging from salad dressings to condiments, soups and sauces.


Vinegar is also used as a food preservative and pickling agent.
Plus, it can even be used to make natural cleaning products, skin toners, bug sprays and more.
Some medications contain acetic acid, including those used to treat ear infections.


Some also use Acetic Acid in the treatment of other conditions, including warts, lice and fungal infections, although more research is needed to evaluate its safety and effectiveness.
Acetic acid is also used by manufacturers to create a variety of different products.


In particular, acetic acid is used to make chemical compounds like vinyl acetate monomer as well as perfumes, oral hygiene products, skin care products, inks and dyes.
Release to the environment of Acetic Acid can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).


Other release to the environment of Acetic Acid is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).


Acetic Acid can be found in products with material based on: paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), leather (e.g. gloves, shoes, purses, furniture), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys) and wood (e.g. floors, furniture, toys).


Acetic Acid is used in the following products: laboratory chemicals, pH regulators and water treatment products, water treatment chemicals, plant protection products and washing & cleaning products.
Acetic Acid is used in the following areas: formulation of mixtures and/or re-packaging.


Acetic Acid is used for the manufacture of: chemicals.
Other release to the environment of Acetic Acid is likely to occur from: outdoor use and indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).


Acetic Acid is used in the following products: coating products, perfumes and fragrances, paper chemicals and dyes, textile treatment products and dyes, metal surface treatment products, non-metal-surface treatment products and polymers.
Acetic Acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Release to the environment of Acetic Acid can occur from industrial use: formulation of mixtures, formulation in materials, manufacturing of the substance, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, for thermoplastic manufacture, as processing aid, of substances in closed systems with minimal release and in the production of articles.


Acetic Acid is used in the following products: laboratory chemicals, pH regulators and water treatment products, oil and gas exploration or production products, water treatment chemicals, washing & cleaning products, polymers and coating products.
Acetic Acid is used in the following areas: mining and formulation of mixtures and/or re-packaging.


Acetic Acid is used for the manufacture of: chemicals, textile, leather or fur, wood and wood products and pulp, paper and paper products.
Release to the environment of Acetic Acid can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and manufacturing of the substance.


Release to the environment of Acetic Acid can occur from industrial use: manufacturing of the substance, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), formulation of mixtures, formulation in materials, in the production of articles, as processing aid, for thermoplastic manufacture, as processing aid and of substances in closed systems with minimal release.


Acetic Acid is used in the following products: coating products, washing & cleaning products, air care products, lubricants and greases, fillers, putties, plasters, modelling clay, anti-freeze products, fertilisers, plant protection products, finger paints, biocides (e.g. disinfectants, pest control products), welding & soldering products and textile treatment products and dyes.


Other release to the environment of Acetic Acid is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).


Industrially, acetic acid is used in the preparation of metal acetates, used in some printing processes; vinyl acetate, employed in the production of plastics; cellulose acetate, used in making photographic films and textiles; and volatile organic esters (such as ethyl and butyl acetates), widely used as solvents for resins, paints, and lacquers.


Biologically, acetic acid is an important metabolic intermediate, and it occurs naturally in body fluids and in plant juices.
Aside from its uses as a natural preservative and common ingredient in a variety of products, acetic acid has also been associated with several impressive health benefits.


In addition to its potent anti-bacterial properties, Acetic Acid is also thought to reduce blood sugar levels, promote weight loss, alleviate inflammation and control blood pressure.
As chemical distributors, the purposes for which this type of Acetic Acid is processed are varied.


As mentioned above, Acetic Acid can be found in many grocery shops as white vinegar.
In such products, acetic acid cannot be found in its pure form, but only in small quantities.
Acetic Acid is also present in foods such as canned and pickled foods, cheese and dairy products, sauces or prepared salads.


Acetic Acid is also commonly used in the pharmaceutical, cosmetic and industrial industries both to produce other substances and to regulate their properties, especially with regards to their pH.
Due to its strong odour, one of its other main uses is in cosmetics as a regulator in the aroma of fragrances, i.e. Acetic Acid achieves a balance between sweet smells in particular.


In the textile industry, Acetic Acid is used to dye fabrics and produce fabrics such as viscose or latex.
In the chemical industry, acetic acid is used in the production of cleaning products and, in the pharmaceutical industry, in supplements and some medicines, as it is capable of stabilising blood pressure and reducing blood sugar levels.


Acetic Acid is also a common ingredient in ointments.
In households diluted acetic acid is often used as a cleaning agent. In the food industry acetic acid is used as an acidity regulator.
Acetic Acid is used to make other chemicals, as a food additive, and in petroleum production.


Acetic Acid is used locally, occasionally internally, as a counterirritant and also as a reagent.
Acetic acid otic (for the ear) is an antibiotic that treats infections caused by bacteria or fungus.
In households, diluted acetic acid is often used in descaling agents.


In the food industry, acetic acid is controlled by the food additive code E260 as an acidity regulator and as a condiment.
In biochemistry, the acetyl group, derived from acetic acid, is fundamental to all forms of life.
When bound to coenzyme A, Acetic Acid is central to the metabolism of carbohydrates and fats.


The global demand for acetic acid is about 6.5 million metric tonnes per year (t/a), manufactured from methanol.
Acetic Acid's production and subsequent industrial use poses health hazards to workers, including incidental skin damage and chronic respiratory injuries from inhalation.


Acetic acid is a chemical reagent for the production of chemical compounds.
The largest single use of acetic acid is in the production of vinyl acetate monomer, closely followed by acetic anhydride and ester production.
The volume of acetic acid used in vinegar is comparatively small.


In the field of analytical chemistry, glacial acetic acid is widely used in order to estimate substances that are weakly alkaline.
Acetic Acid has a wide range of applications as a polar, protic solvent.
Acetic acid is used as an antiseptic due to its antibacterial qualities


The manufacture of rayon fiber involves the use of Acetic Acid.
Medically, acetic acid has been employed to treat cancer by its direct injection into the tumour.
Being the major constituent of vinegar, Acetic Acid finds use in the pickling of many vegetables.


The manufacture of rubber involves the use of Acetic Acid.
Acetic Acid is also used in the manufacture of various perfumes.
Acetic Acid is widely used in the production of VAM (vinyl acetate monomer).


When two molecules of acetic acid undergo a condensation reaction together, the product formed is acetic anhydride.
Acetic Acid is widely used in the industrial preparation of dimethyl terephthalate (DMT).
Acetic acid is used in the manufacture of acetic anhydride, cellulose acetate, vinyl acetate monomer, acetic esters, chloracetic acid, plastics, dyes, insecticides, photographic chemicals, and rubber.


Other commercial uses of Acetic Acid include the manufacture of vitamins, antibiotics, hormones, and organic chemicals, and as a food additive (acidulant).
Acetic Acid is also used in various textile printing processes.
Acetic acid is the main component of vinegar, which contains 4 to 18% acetic acid.


Acetic Acid is used as a food preservative and food additive (known as E260).
Acetic acid is used as a raw material and solvent in the production of other chemical products, in oil and gas production, and in the food and pharmaceutical industries.


Large quantities of acetic acid are used to make products such as ink for textile printing, dyes, photographic chemicals, pesticides, pharmaceuticals, rubber and plastics.
Acetic Acid is also used in some household cleaning products to remove lime scale.


In foods, Acetic acid is used for its antibacterial properties, as an acidity stabiliser, diluting colours, as a flavouring agent and for inhibiting mould growth in bread.
In brewing, Acetic acid is used to reduce excess losses of carbohydrate from the germinated barley and to compensate for production variations, so producing a consistent quality beer.


Acetic acid can be found in beer, bread, cheese, chutney, horseradish cream, pickles, salad cream, brown sauce, fruit sauce, mint sauce and jelly and tinned baby food, sardines and tomatoes.
Acetic acid is often used as table vinegar.


Acetic acid is also used directly as a condiment, and in the pickling of vegetables and other foods.
Acetic acid is used as the main component in the subsequent synthesis in the process of food and pharmaceutical production.
Food additive Acetic acid is widely used in marinating, canning, making mayonnaise and sauces and other foods.


In one of Acetic acid's most common form, vinegar is also used directly as a condiment, and in the pickling of vegetables and other foods to preserve food against bacteria and fungi.
In brewing, Acetic acid is used to reduce excess losses of carbohydrate from the germinated barley and to compensate for production variations, so producing a consistent quality beer.


When used as food additive, Acetic acid has a E number 260.
Acetic acid can be found in beer, bread, cheese, chutney, horseradish cream, pickles, salad cream, brown sauce, fruit sauce, mint sauce and jelly and tinned baby food, sardines and tomatoes.


Acetic acid is approved to use as food addictive in EU and generally recognized as safe food substance in the US.
In addition to vinegar, Acetic acid is used as a food additive and preservative in a variety of other foods, including baked goods, processed meats, cheeses, and condiments.


Many pickled foods, like pickles and sauerkraut, also contain Acetic acid as a natural byproduct of the fermentation process.
Acetic acid is also used in the production of various food ingredients, including salts, esters, and anhydrides.
These derivatives of Acetic acid are used as preservatives, flavorings, and emulsifiers in processed foods.


Some examples of these derivatives include sodium acetate, ethyl acetate, and acetic anhydride.
Acetic acid is also used in the production of various adhesives, coatings, and inks, and is used to produce cellulose acetate, which is used in photographic films and other applications.


Acetic acid is found naturally in many foods and is also produced synthetically for a variety of industrial applications.
Derivatives of Acetic acid are used as food additives and preservatives, as well as in the production of various chemicals and materials.
Acetic acid is one of the simplest carboxylic acid.


It has a variety of uses, ranging from food and medical to industrial.
As mentioned earlier, Acetic acid is primarily found in vinegar.
Acetic acid's also used as food additive (E number E260) for regulating acidity and as a preservative.


Acetic acid is also essential in the pickling process, which involves preserving vegetables or fruits (such as cucumbers, beets, or watermelon rind) in vinegar.
Acetic acid helps to prevent the growth of harmful bacteria and preserves the vegetables or fruits' natural color, flavor, and texture.


Pickling is a common technique used to preserve foods, especially in countries with long winter seasons where fresh produce is not available.
Acetic acid is used in the production of a wide range of chemicals and materials, such as vinyl acetate monomer (VAM), cellulose acetate, and acetic anhydride.


These chemicals are used in various industries, including textiles, plastics, coatings, and adhesives.
Acetic acid can also be used to produce synthetic fabrics that resemble natural ones such as silk, wool or cotton.
Acetic acid can be used to increase the acidity (and lower the pH) of food products as well as improve the organoleptic quality by giving the product an acid flavor, such as salt and vinegar chips.


Acetic acid is also a popular preservative as it stops bacterial growth in dressings, sauces, cheese, and pickles.
Acetic acid/vinegar is used to pickle foods, which is a type of preservation method. When used with baking soda, acetic acid also works as a chemical leavening agent.


Besides food, Acetic acid has been used in medicine, such as in ear drops, and a number of industrial processes.
Acetic acid is used to make cellulose acetate and polyvinyl acetate and glacial acetic acid in particular is frequently used as a solvent.
As mentioned before, Acetic acid is extensively used as a food preservative.


Acetic acid makes foods less hospitable to harmful bacteria that can cause food poisoning.
When used in small amounts, Acetic acid can effectively extend the shelf life of food items.
Furthermore, Acetic acid can also be added to pickling liquid to help maintain the pickled product's acidity level, thereby making it last longer.


Another popular application of Acetic acid is as a natural food flavour enhancer.
Along with improving the taste of many processed foods including sauces, dressings, and condiments, Acetic acid is also used to provide a sour tang to beverages like soda and energy drinks.


Acetic acid is added in small amounts to these products in order to impart a tart, refreshing taste that many consumers prefer.
Acetic acid is used in a wide variety of household cleaning products, including all-purpose cleaners, glass cleaners, and bathroom cleaning solutions.
In addition to its use in household cleaners, Acetic acid is also used as a natural weed killer.


Acetic acid can be sprayed on weeds in gardens and lawns to kill them without contaminating the soil.
Some environmentally conscious gardeners prefer using vinegar sprays instead of toxic chemical herbicides, as Acetic acid is considered a more eco-friendly solution.


Some research has also shown that Acetic acid may have potential health benefits.
For instance, Acetic acid has been studied for its potential to lower blood sugar levels and improve insulin sensitivity.
In addition, Acetic acid may help with weight loss by reducing appetite and promoting feelings of fullness.


However, more research is needed to fully understand the potential health benefits of Acetic acid.
In terms of safety, Acetic acid should be handled with care.
To summarize, Acetic acid is a versatile ingredient with numerous applications.


Acetic acid is commonly used as a food preservative, flavour enhancer, and cleaning agent.
Acetic acid also has potential health benefits, although further research is needed to confirm these benefits.
As with any chemical, Acetic acid should be handled with care and stored properly to minimize risk of injury or damage to property.


In conclusion, Acetic acid is a widely-used food ingredient with many applications and benefits.
Acetic acid is a natural substance that is safe when used appropriately.
Whether you're using it in the kitchen or for cleaning purposes, Acetic acid is a versatile and effective solution that has been relied upon for centuries.


Acetic acid is a versatile and widely-used food ingredient with a range of possible benefits and applications, as well as a few drawbacks.
Understanding the properties and uses of Acetic acid is essential for anyone working with food or chemicals.
In addition to Acetic acid, there are other types of acids that are used in food production, such as ascorbic acid (vitamin C), citric acid, and malic acid.


These acids are commonly used as preservatives, stabilizers, flavor enhancers, and acidulants, depending on the specific product formulation.
While each type of acid has its own unique properties, Acetic acid stands out for its sour taste and pungent aroma.
One of the key applications of Acetic acid is in the production of vinegar, which is a widely-used condiment that is made by fermenting ethanol and other sugars.


Apple cider vinegar, balsamic vinegar, and white vinegar are some of the most popular vinegar varieties available.
Each type of vinegar has Acetic acid's own unique flavor and can be used in a range of recipes, from marinades to salad dressings.
Acidity regulator Acetic acid is commonly used in food as a preservative and flavoring agent.


Acetic acid is primarily used to regulate the acidity levels in various food products, including pickles, sauces, dressings, and condiments.
Additionally, acidity regulator Acetic acid is effective in preventing the growth of bacteria and fungi in food, extending its shelf life.
Acetic acid is considered safe for consumption when used within the approved limits set by regulatory authorities.


Acetic acid is commonly used in pickled vegetables, dressings, sauces, and condiments to provide tartness and enhance flavors.
Acetic acid has been used in food preservation and flavoring for centuries.
Acetic acid is a commonly used additive in the food industry.


Acetic acid is a natural acid found in vinegar and is widely used as a food preservative and flavoring agent.
Acetic acid is known for its sour taste and is often added to various food products such as pickles, sauces, condiments, and dressings to enhance their flavor and extend their shelf life.


As a food preservative, Acetic acid works by creating an acidic environment that inhibits the growth of bacteria and other microorganisms.
This helps to prevent food spoilage and increase Acetic acid's stability.
Acetic acid also acts as a pH regulator, helping to maintain the desired acidity level in certain foods.


As with any food additive, it is recommended to consume foods containing Acetic acid in moderation and as part of a balanced diet.
In conclusion, Acetic acid is a widely used food additive that serves both as a preservative and a flavor enhancer.
Acetic acid provides a sour taste and helps to extend the shelf life of various food products.



-Acetic acid with formula CH3COOH or food additive E260 is used:
*food industry – known as additive E260, is involved in the production of dairy products, salads, sauces, dressings, marinades and canned food;
*Pharmaceutical industry – is part of aspirin, phenacetin, other drugs and dietary supplements that stabilize blood pressure and reduce blood sugar;
*textile industry – as a component for the manufacture and dyeing of rayon, latex fabrics;
*cosmetic sphere – used to balance the smell and regulate the characteristics of various compositions;
*chemical industry – production of cleaning and detergents, household chemicals, acetone, synthetic dyes;
*as a solvent for varnishes, latex coagulant;
*as an acetylating agent in organic synthesis;
*salts of acetic acid (Fe, Al, Cr, etc.) – mordants for dyeing, etc.


-Breeding of bees:
Acetic acid fumigation will kill a wide variety of pathogens, such as the causative agents of Cretaceous brood, European foulbrood, Nosema and Amoeba.
Acetic Acid will also eliminate all stages of the wax moth except the pupae.


-Vinyl acetate monomer:
Production of vinyl acetate monomer (VAM), the application consumes approximately 40% to 45% of the world's acetic acid production.
The reaction is with ethylene and acetic acid with oxygen over a palladium catalyst.


-Ester production:
Acetic acid esters are used as a solvent in inks, paints and coatings.
Esters include ethyl acetate, n-butyl acetate, isobutyl acetate, and propyl acetate


-Use as a solvent:
Acetic Acid is an excellent polar protic solvent.
Acetic Acid is often used as a recrystallization solvent to purify organic compounds.
Acetic Acid is used as a solvent in the production of terephthalic acid (TPA), a raw material for the production of polyethylene terephthalate (PET).


-Medical use of Acetic acid:
Acetic acid injection into a tumor has been used to treat cancer since the 1800s.
Acetic acid is used as part of cervical cancer screening in many areas in the developing world.

The acid is applied to the cervix and if an area of white appears after about a minute the test is positive.
Acetic acid is an effective antiseptic when used as a 1% solution, with broad spectrum of activity against streptococci, staphylococci, pseudomonas, enterococci and others.

Acetic Acid may be used to treat skin infections caused by pseudomonas strains resistant to typical antibiotics.
While diluted acetic acid is used in iontophoresis, no high quality evidence supports this treatment for rotator cuff disease.
As a treatment for otitis externa, it is on the World Health Organization's List of Essential Medicines.


-Foods uses of Acetic acid:
Acetic acid has 349 kcal (1,460 kJ) per 100 g.
Vinegar is typically no less than 4% acetic acid by mass.
Legal limits on acetic acid content vary by jurisdiction.

Vinegar is used directly as a condiment, and in the pickling of vegetables and other foods.
Table vinegar tends to be more diluted (4% to 8% acetic acid), while commercial food pickling employs solutions that are more concentrated.
The proportion of acetic acid used worldwide as vinegar is not as large as industrial uses, but it is by far the oldest and best-known application.


-Acetic Acid as a Solvent:
In its liquid state, CH3COOH is a hydrophile (readily dissolves in water) and also a polar, protic solvent.
A mixture of acetic acid and water is, in this manner, similar to a mixture of ethanol and water.
Acetic acid also forms miscible mixtures with hexane, chloroform, and several oils.
However, Acetic Acid does not form miscible mixtures with long-chain alkanes (such as octane).


-Vinyl acetate monomer:
The primary use of acetic acid is the production of vinyl acetate monomer (VAM).
In 2008, this application was estimated to consume a third of the world's production of acetic acid.

The reaction consists of ethylene and acetic acid with oxygen over a palladium catalyst, conducted in the gas phase.
2 H3C−COOH + 2 C2H4 + O2 → 2 H3C−CO−O−CH=CH2 + 2 H2O
Vinyl acetate can be polymerised to polyvinyl acetate or other polymers, which are components in paints and adhesives


-Ester production:
The major esters of acetic acid are commonly used as solvents for inks, paints and coatings.
The esters include ethyl acetate, n-butyl acetate, isobutyl acetate, and propyl acetate.

They are typically produced by catalyzed reaction from acetic acid and the corresponding alcohol:
CH3COO−H + HO−R → CH3COO−R + H2O, R = general alkyl group
For example, acetic acid and ethanol gives ethyl acetate and water.
CH3COO−H + HO−CH2CH3 → CH3COO−CH2CH3 + H2O

Most acetate esters, however, are produced from acetaldehyde using the Tishchenko reaction.
In addition, ether acetates are used as solvents for nitrocellulose, acrylic lacquers, varnish removers, and wood stains.
First, glycol monoethers are produced from ethylene oxide or propylene oxide with alcohol, which are then esterified with acetic acid.

The three major products are ethylene glycol monoethyl ether acetate (EEA), ethylene glycol monobutyl ether acetate (EBA), and propylene glycol monomethyl ether acetate (PMA, more commonly known as PGMEA in semiconductor manufacturing processes, where it is used as a resist solvent).
This application consumes about 15% to 20% of worldwide acetic acid.
Ether acetates, for example EEA, have been shown to be harmful to human reproduction.


-Acetic anhydride:
The product of the condensation of two molecules of acetic acid is acetic anhydride.
The worldwide production of acetic anhydride is a major application, and uses approximately 25% to 30% of the global production of acetic acid.
The main process involves dehydration of acetic acid to give ketene at 700–750 °C.

Ketene is thereafter reacted with acetic acid to obtain the anhydride:
CH3CO2H → CH2=C=O + H2O
CH3CO2H + CH2=C=O → (CH3CO)2O

Acetic anhydride is an acetylation agent.
As such, Acetic Acid's major application is for cellulose acetate, a synthetic textile also used for photographic film.
Acetic anhydride is also a reagent for the production of heroin and other compounds.


-Use as solvent:
As a polar protic solvent, acetic acid is frequently used for recrystallization to purify organic compounds.
Acetic acid is used as a solvent in the production of terephthalic acid (TPA), the raw material for polyethylene terephthalate (PET).
In 2006, about 20% of acetic acid was used for TPA production.

Acetic acid is often used as a solvent for reactions involving carbocations, such as Friedel-Crafts alkylation.
For example, one stage in the commercial manufacture of synthetic camphor involves a Wagner-Meerwein rearrangement of camphene to isobornyl acetate; here acetic acid acts both as a solvent and as a nucleophile to trap the rearranged carbocation.


-Vinegar:
The vinegar is usually 4-18 wt.% Acetic Acid.
Acetic Acid is used directly as a seasoning and marinade of vegetables and other food products.
Table vinegar is used more often more diluted (4% to 8% acetic acid), while a more concentrated solution is used for pickling in commercial foods.


-Industrial Use:
Acetic acid is used in many industrial processes for the production of substrates and it is often used as a chemical reagent for the production of a number of chemical compounds like acetic anhydride, ester, vinyl acetate monomer, vinegar, and many other polymeric materials.
Acetic Acid is also used to purify organic compounds as it can be used as a solvent for recrystallization.


-Industrial applications of Acetic Acid:
As one of the important organic acids, acetic acid is mainly used in the synthesis of vinyl acetate, cellulose acetate, acetic anhydride, acetate, metal acetate and halogenated acetic acid.

Glacial acetic acid is also an important raw material for pharmaceuticals, dyes, pesticides and other organic synthesis.
In addition, Acetic Acid is also widely used in the manufacture of photographic medicines, cellulose acetate, fabric printing and dyeing, and the rubber industry.


-Food applications of Acetic Acid:
In the food industry, acetic acid is generally used as an acidulant, flavor enhancer and spice manufacturing.

*Synthetic vinegar:
Dilute acetic acid to 4-5% with water, add various flavoring agents, the flavor is similar to alcohol vinegar, the production time is short, and the price is cheap.

As a sour agent, glacial acetic acid can be used in compound seasonings, prepared vinegar, canned food, jelly and cheese, and used in moderation according to production needs.
Acetic Acid can also be used as a flavor enhancer, and the recommended dosage is 0.1-0.3 g/kg.


-Medical Use:
Acetic acid has a lot of uses in the medical field.
The most important uses here are that Acetic Acid can be used as an antiseptic against pseudomonas, enterococci, streptococci, staphylococci, and others.
Acetic Acid is also used in cervical cancer screening and for the treatment of infections.
Further, Acetic Acid is used as an agent to lyse red blood cells before white blood cells are examined.
Vinegar has also been said to reduce high concentrations of blood sugar.


-Important and Popular Uses of Acetic Acid:
There are many uses of acetic acid.
So, in addition to being treated just as a food preservative (vinegar), the acid is used in many areas and instances.

Some top and important uses include:
*Industrial Use
*Medicinal Uses
*Household
*Food Industry


-Food Industry:
In the food industry, acetic acid finds its use most commonly in commercial pickling operations, and in condiments like mayonnaise, mustard, and ketchup.
Acetic Acid is also used for seasoning various food items like salads etc.
Additionally, vinegar can react with alkaline ingredients like baking soda and when that happens it produces a gas that helps to make baked goods become.


-Household Uses:
Acetic acid which is a dilute solution is used extensively as vinegar.
And as we are familiar, vinegar is widely used for cleaning, laundry, cooking, and many other household uses.

Farmers usually spray acetic acid on livestock silage to counter bacterial and fungal growth.
Apart from these, acetic acid is used for the manufacture of inks and dyes and it is also used in making perfumes.
Acetic Acid is also involved in the manufacturing of rubber and plastic industries.


-Acetic acid with formula CH3COOH or food additive E260 is used:
*food industry – known as additive E260, is involved in the production of dairy products, salads, sauces, dressings, marinades and canned food;
*Pharmaceutical industry – is part of aspirin, phenacetin, other drugs and dietary supplements that stabilize blood pressure and reduce blood sugar;
*textile industry – as a component for the manufacture and dyeing of rayon, latex fabrics;
*cosmetic sphere – used to balance the smell and regulate the characteristics of various compositions;
*chemical industry – production of cleaning and detergents, household chemicals, acetone, synthetic dyes;
*as a solvent for varnishes, latex coagulant;
*as an acetylating agent in organic synthesis;
*salts of acetic acid (Fe, Al, Cr, etc.) – mordants for dyeing, etc.



INDUSTRIAL APPLICATION OF ACETIC ACID:
Thanks to its versatile properties, Acetic acid plays a vital role in various European industries.

*In the chemical industry, Acetic acid is a fundamental building block for producing numerous chemicals.
One example is vinyl acetate monomer (VAM), which Acetic acid is widely used to manufacture adhesives, paints, and coatings.
Acetic acid is also an essential precursor for producing acetic anhydride, esters, and cellulose acetate.

*The food and beverage industry extensively utilizes Acetic acid as a preservative and flavoring agent.
Vinegar, primarily composed of Acetic acid, finds widespread use in cooking, pickling, and salad dressings.

*In the pharmaceutical industry, Acetic acid is a crucial intermediate in synthesizing pharmaceuticals, including antibiotics, vitamins, and analgesics.
Acetic acid's versatile nature allows for the production of a wide range of medications.

*The textile industry relies on Acetic acid to manufacture synthetic acetate fibers.
Acetate fibers are commonly used in clothing, upholstery, and textiles due to their excellent draping properties and durability.



USES AND BENEFITS OF ACETIC ACID:
One of the most common ways consumers may come into contact with acetic acid is in the form of household vinegar, which is naturally made from fermentable sources such as wine, potatoes, apples, grapes, berries and grains.

Vinegar is a clear solution generally containing about 5 percent acetic acid and 95 percent water.
Vinegar is used as a food ingredient and can also be an ingredient in personal care products, household cleaners, pet shampoos and many other products for the home:

-vinegar and baking soda
*Food Preparation:
Vinegar is a common food ingredient, often used as a brine in pickling liquids, vinaigrettes, marinades and other salad dressings.
Vinegar also can be used in food preparation to help control Salmonella contamination in meat and poultry products.

*Cleaning:
Vinegar can be used throughout the home as a window cleaner, to clean automatic coffee makers and dishes, as a rinsing agent for dishwashers, and to clean bathroom tile and grout.
Vinegar can also be used to clean food-related tools and equipment because it generally does not leave behind a harmful residue and requires less rinsing.

*Gardening:
In concentrations of 10 to 20 percent, acetic acid can be used as a weed killer on gardens and lawns.
When used as an herbicide, the acetic acid can kill weeds that have emerged from the soil, but does not affect the roots of the weed, so they can regrow.

When acetic acid is at 99.5 percent concentration, it is referred to as glacial acetic acid.
Glacial acetic acid has a variety of uses, including as a raw material and solvent in the production of other chemical products.



INDUSTRIAL APPLICATIONS FOR ACETIC ACID INCLUDE:
*Vinyl Acetate, cellulose fibers and plastics:
Acetic acid is used to make many chemicals, including vinyl acetate, acetic anhydride and acetate esters.
Vinyl acetate is used to make polyvinyl acetate, a polymer used in paints, adhesives, plastics and textile finishes.

Acetic anhydride is used in the manufacture of cellulose acetate fibers and plastics used for photographic film, clothing and coatings.
Acetic acid is also used in the chemical reaction to produce purified terephthalic acid (PTA), which is used to manufacture the PET plastic resin used in synthetic fibers, food containers, beverage bottles and plastic films.

*Solvents:
Acetic acid is a hydrophilic solvent, similar to ethanol.
Acetic Acid dissolves compounds such as oils, sulfur and iodine and mixes with water, chloroform and hexane.

*Acidizing oil and gas:
Acetic acid can help reduce metal corrosion and scale build-up in oil and gas well applications.
Acetic Acid is also used in oil well stimulation to improve flow and increase production of oil and gas.

*Pharmaceuticals and vitamins:
The pharmaceutical industry uses acetic acid in the manufacture of vitamins, antibiotics, hormones and other products.

*Food Processing:
Acetic acid is commonly used as a cleaning and disinfecting product in food processing plants.

*Other uses:
Salts of acetic acid and various rubber and photographic chemicals are made from acetic acid.
Acetic acid and its sodium salt are commonly used as a food preservative.



WHAT CAN YOU USE ACETIC ACID FOR?
*Removing stubborn limescale on sanitary facilities and kitchen appliances.
*Combating green deposits on terraces, garden furniture and stone surfaces.
*Descaling of industrial machines and equipment.
*Cleaning and disinfection in the food industry, if adequately diluted.
*Use as raw material in chemical synthesis for the production of esters, acetic esters and various organic compounds.
*In agriculture for regulating the pH value of the soil.
*As a preservative in food processing, for example when pickling vegetables.
*Cleaning and restoration of facades and monuments.



USES OF ACETIC ACID:
The chemical reagent for the processing of chemical compounds is acetic acid.
In the production of vinyl acetate monomer, acetic anhydride, and ester production, the use of acetic acid is important.


*Vinyl Acetate Monomer:
Vinyl acetate monomer (VAM) processing is the main application of acetic acid.
Vinyl acetate undergoes polymerization to produce polyvinyl acetate or other polymers, which are components of paints and adhesives.

The reaction consists of ethylene and acetic acid with oxygen over a palladium catalyst.
2CH3COOH+2C2H4+O2→2CH3CO2CH=CH2+2H2O
Wood glue also utilizes vinyl acetate polymers.

*Acetic Anhydride:
Acetic anhydride is the result of the condensation of two acetic acid molecules.
Significant use is the worldwide processing of acetic anhydride, utilizing about 25 per cent to 30 per cent of global acetic acid production.
The key method includes acetic acid dehydration to give ketene at 700-750 °C.

CH3CO2H→CH2=C=O+H2O
CH3CO2H+CH2=C=O→CH3CO2O

It is great for general disinfection and fighting mould and mildew since acetic acid kills fungi and bacteria.
Acetic Acid is useful in a range of traditional and green cleaning materials, such as mould and mildew cleaners, floor cleaners, sprays for cleaning and dusting, and roof cleaners, either as vinegar or as an element.

The acetyl group is in use widely in the biochemistry field.
Products made from acetic acid are an effective metabolizer of carbohydrates and fats when bound to coenzyme A.
As a treatment for otitis externa, Acetic Acid is the best and most effective drug in a health system on the World Health Organization’s List of Essential Medicines.



ACETIC ACID IN EVERYDAY LIFE:
Acetic Acid is found in many everyday products as described above, such as food, cleaning products and cosmetics, among others.
Of all of them, vinegar is one of the most important ones, as Acetic Acid has different uses, such as for cooking or cleaning.
Acetic Acid is an infallible product when it comes to dealing with stubborn stains such as dog urine, rust or other dirt.



PHYSICAL PROPERTIES OF ACETIC ACID:
Acetic acid is a colorless liquid; with a strong vinegar-like odour.
Acetic acid is considered a volatile organic compound by the National Pollutant Inventory.
Specific Gravity: 1.049 @ 25°C
Melting Point: 16.7°C
Boiling Point: 118°C
Vapour pressure: 1.5 kPa @ 20°C



CHEMICAL PROPERTIES OF ACETIC ACID:
Acetic acid is hygroscopic, meaning that it tends to absorb moisture.
Acetic Acid mixes with ethyl alcohol, glycerol, ether, carbon tetrachloride and water and reacts with oxidants and bases.
Concentrated acetic acid is corrosive and attacks many metals forming flammable or explosive gases.
Acetic Acid can also attack some forms of plastic, rubber and coatings.



HEALTH BENEFITS OF ACETIC ACID:
1. Kills Bacteria:
Vinegar has long been used as a natural disinfectant, largely due to its content of acetic acid.
Acetic acid has powerful antibacterial properties and can be effective at killing off several specific strains of bacteria.

In fact, one 2014 in vitro study found that acetic acid was able to block the growth of myobacteria, a genus of bacteria responsible for causing tuberculosis and leprosy.
Other research shows that vinegar may also protect against bacterial growth, which may be partially due to the presence of acetic acid.


2. Reduces Blood Pressure:
Not only does high blood pressure place extra strain on the heart muscle and cause it to slowly weaken over time, but high blood pressure is also a major risk factor for heart disease.
In addition to modifying your diet and exercise routine, promising research has found that acetic acid may also help control blood pressure.


3. Decreases Inflammation:
Acute inflammation plays an important role in immune function, helping to defend the body against illness and infection.
Sustaining high levels of inflammation long-term, however, can have a detrimental effect on health, with studies showing that inflammation could contribute to the development of chronic conditions like heart disease and cancer.
Acetic acid is thought to reduce inflammation to help protect against disease.


4. Supports Weight Loss:
Some research suggests that acetic acid could help support weight control by aiding in weight loss.


5. Promotes Blood Sugar Control:
Apple cider vinegar has been well-studied for its ability to support blood sugar control.
Research shows that acetic acid, one of the primary components found in apple cider vinegar, may play a role in its powerful blood sugar-lowering properties.

In one study, consuming vinegar with acetic acid alongside a high-carb meal was found to reduce blood sugar and insulin levels thanks to its ability to slow down the emptying of the stomach.
Another in vitro study had similar findings, reporting that acetic acid decreased the activity of several enzymes involved in carbohydrate metabolism, which could decrease the absorption of carbs and sugar in the small intestine.



NOMENCLATURE OF ACETIC ACID:
The trivial name "acetic acid" is the most commonly used and preferred IUPAC name.
The systematic name "ethanoic acid", a valid IUPAC name, is constructed according to the substitutive nomenclature.
The name "acetic acid" derives from the Latin word for vinegar, "acetum", which is related to the word "acid" itself.

"Glacial acetic acid" is a name for water-free (anhydrous) acetic acid.
Similar to the German name "Eisessig" ("ice vinegar"), the name comes from the solid ice-like crystals that form with agitation, slightly below room temperature at 16.6 °C (61.9 °F).

Acetic acid can never be truly water-free in an atmosphere that contains water, so the presence of 0.1% water in glacial acetic acid lowers its melting point by 0.2 °C.
A common symbol for acetic acid is AcOH (or HOAc), where Ac is the pseudoelement symbol representing the acetyl group CH3−C(=O)−; the conjugate base, acetate (CH3COO−), is thus represented as AcO−.

(The symbol Ac for the acetyl functional group is not to be confused with the symbol Ac for the element actinium; context prevents confusion among organic chemists).
To better reflect its structure, acetic acid is often written as CH3−C(O)OH, CH3−C(=O)OH, CH3COOH, and CH3CO2H.

In the context of acid–base reactions, the abbreviation HAc is sometimes used, where Ac in this case is a symbol for acetate (rather than acetyl).
Acetate is the ion resulting from loss of H+ from acetic acid.
The name "acetate" can also refer to a salt containing this anion, or an ester of acetic acid.



HISTORY OF ACETIC ACID:
Vinegar was known early in civilization as the natural result of exposure of beer and wine to air because acetic acid-producing bacteria are present globally.
The use of acetic acid in alchemy extends into the third century BC, when the Greek philosopher Theophrastus described how vinegar acted on metals to produce pigments useful in art, including white lead (lead carbonate) and verdigris, a green mixture of copper salts including copper(II) acetate.

Ancient Romans boiled soured wine to produce a highly sweet syrup called sapa.
Sapa that was produced in lead pots was rich in lead acetate, a sweet substance also called sugar of lead or sugar of Saturn, which contributed to lead poisoning among the Roman aristocracy.

In the 16th-century German alchemist Andreas Libavius described the production of acetone from the dry distillation of lead acetate, ketonic decarboxylation.

The presence of water in vinegar has such a profound effect on acetic acid's properties that for centuries chemists believed that glacial acetic acid and the acid found in vinegar were two different substances.
French chemist Pierre Adet proved them identical.


*Crystallised acetic acid
In 1845 German chemist Hermann Kolbe synthesised acetic acid from inorganic compounds for the first time.
This reaction sequence consisted of chlorination of carbon disulfide to carbon tetrachloride, followed by pyrolysis to tetrachloroethylene and aqueous chlorination to trichloroacetic acid, and concluded with electrolytic reduction to acetic acid.

By 1910, most glacial acetic acid was obtained from the pyroligneous liquor, a product of the distillation of wood.
The acetic acid was isolated by treatment with milk of lime, and the resulting calcium acetate was then acidified with sulfuric acid to recover acetic acid.
At that time, Germany was producing 10,000 tons of glacial acetic acid, around 30% of which was used for the manufacture of indigo dye.

Because both methanol and carbon monoxide are commodity raw materials, methanol carbonylation long appeared to be attractive precursors to acetic acid.
Henri Dreyfus at British Celanese developed a methanol carbonylation pilot plant as early as 1925.

However, a lack of practical materials that could contain the corrosive reaction mixture at the high pressures needed (200 atm or more) discouraged commercialization of these routes.
The first commercial methanol carbonylation process, which used a cobalt catalyst, was developed by German chemical company BASF in 1963.

In 1968, a rhodium-based catalyst (cis−[Rh(CO)2I2]−) was discovered that could operate efficiently at lower pressure with almost no by-products.
US chemical company Monsanto Company built the first plant using this catalyst in 1970, and rhodium-catalyzed methanol carbonylation became the dominant method of acetic acid production (see Monsanto process).

In the late 1990s, BP Chemicals commercialised the Cativa catalyst ([Ir(CO)2I2]−), which is promoted by iridium for greater efficiency.
Known as the Cativa process, the iridium-catalyzed production of glacial acetic acid is greener, and has largely supplanted the Monsanto process, often in the same production plants.


*Interstellar medium
Interstellar acetic acid was discovered in 1996 by a team led by David Mehringer using the former Berkeley-Illinois-Maryland Association array at the Hat Creek Radio Observatory and the former Millimeter Array located at the Owens Valley Radio Observatory.

It was first detected in the Sagittarius B2 North molecular cloud (also known as the Sgr B2 Large Molecule Heimat source).
Acetic acid has the distinction of being the first molecule discovered in the interstellar medium using solely radio interferometers; in all previous ISM molecular discoveries made in the millimetre and centimetre wavelength regimes, single dish radio telescopes were at least partly responsible for the detections.



WHAT IS ACETIC ACID IN FOOD?
Acetic acid is a food additive that is commonly used as a preservative, flavor enhancer, and pH regulator.
Acetic acid is a natural acid found in vinegar and is also produced synthetically for use in food applications.

Acetic acid is generally regarded as safe for consumption at low levels, and it is commonly used in condiments, pickled foods, sauces, and dressings to provide a tangy taste and extend shelf life.
However, excessive consumption of Acetic acid can cause irritation to the digestive system.
As with any food additive, it is important to consume Acetic acid in moderation and maintain a balanced diet.



PHYSICAL DETAILS AND PROPERTIES OF ACETIC ACID:
Acetic acid, or ethanoic acid, is a clear, colorless liquid with a pungent vinegar-like odor.
Acetic acid has a molecular formula CH₃COOH and a molecular weight of 60.05 g/mol.
With a boiling point of 118.1, °C and a melting point of 16.6°C, Acetic acid is highly soluble in water and miscible with most organic solvents.
These physical properties make Acetic acid a versatile compound for various industrial applications.



PRODUCTION METHODS OF ACETIC ACID:
Acetic acid is primarily produced through two main methods: methanol carbonylation and oxidation of acetaldehyde.
The first method, methanol carbonylation, is the most common process for large-scale Acetic acid production.
Acetic acid involves the reaction of methanol with carbon monoxide in the presence of a catalyst, typically rhodium or iodine compounds.

This catalytic reaction yields Acetic acid as the primary product.
The second method involves the oxidation of acetaldehyde. Acetaldehyde can be oxidized using various catalysts, including palladium or copper, producing Acetic acid as a byproduct.



WHAT IS THE PURPOSE OF ACETIC ACID IN ADDITIVES FOODS?
Acetic acid is commonly used as a food additive.
Acetic acid serves multiple purposes in additives foods.
Firstly, Acetic acid acts as a preservative by inhibiting the growth of bacteria and fungi, thus extending the shelf life of the product.
Secondly, Acetic acid enhances the flavor and aroma of the food by giving it a tangy and sour taste.
Additionally, Acetic acid can also be used as an acidity regulator and pH control agent in certain food products.



FUNCTIONS OF ACETIC ACID:
1. Acidity Regulator / Buffering Agent - Changes or maintains the acidity or basicity of food/cosmetics.
2. Drug / Medicine - Treats, alleviates, cures, or prevents sickness. As officially declared by a governmental drug/medicine regulatory body
3. Exfoliant - Removes dead cells at the surface of the skin
4. Experimental / Patented - Relatively new ingredient with limited data available
5. Insecticide / Pesticide - Kills or inhibits unwanted organisms
6. Preservative - Prevents and inhibits the growth of unwanted microorganisms which may be harmful
7. Solvent (Cosmetics) - Enhances the properties of other ingredients



IS ACETIC ACID SAFE?
Acetic acid is also known as acetic acid, which is a widely used food additive.
Acetic acid is considered safe for consumption by regulatory authorities such as the Food and Drug Administration (FDA) and the European Food Safety Authority (EFSA).



HEALTH BENEFITS OF ACETIC ACID:
Acetic acid has powerful antibacterial properties.
Acetic acid helps to reduce blood pressure.
Acetic acid also help to reduce inflammation.
Acetic acid promotes blood sugar control.
Acetic acid also supports weight loss.



FUNCTION & CHARACTERISTICS OF ACETIC ACID:
Acetic acid is used as a preservative against bacteria and fungi.
In mayonnaise Acetic acid is added to increase the inactivation of Salmonella .
The highest activity of Acetic acid is at low pH.
Acetic acid can also be used as a buffer in acidic foods.
Acetic acid is also used as an aroma component.



ORIGIN OF ACETIC ACID:
Natural acid, present in most fruits.
Acetic acid is produced by bacterial fermentation and thus present in all fermented products.
Commercially produced by bacterial fermentation of sugar, molasses or alcohol or by chemical synthesis from acetealdehyde.



IS ACETIC ACID GLUTEN FREE?
Yes.
Acetic acid is gluten free and widely used in gluten free food to provide sour taste to sour drinks.



WHY IS ACETIC ACID GLUTEN FREE?
Gluten is a type of elastic grain protein that helps wheat, rye and barley hold their shape.
Because of its glue-like properties, gluten is often added to other food products—pasta, sauces, crackers, baked goods—to thicken or bind those products together.
Raw materials used in manufacturing of Acetic acid are Acetyl ketene; So the manufacturing process of it is gluten free.
So, Acetic acid is gluten free.



IS ACETIC ACID SAFE FOR CONSUMPTION IN ADDITIVES FOODS?
Acetic acid is considered safe for consumption in additives foods.
Acetic acid is a naturally occurring substance and is commonly found in vinegar.
Acetic acid is used as a flavoring agent and food preservative in various processed foods.
However, Acetic acid is important to note that excessive consumption of acetic acid may have adverse effects on health.
Acetic acid is always recommended to consume additives foods in moderation and as part of a balanced diet.



HOW DOES ACETIC ACID CONTRIBUTE TO THE PRESERVATION OF ADDITIVES FOODS?
Acetic acid contributes to the preservation of additives foods in several ways.
Firstly, Acetic acid has antimicrobial properties that inhibit the growth of bacteria, yeasts, and molds, reducing the risk of food spoilage and extending the shelf life of products.

Additionally, Acetic acid acts as a pH regulator in additives foods.
Acetic acid helps maintain acidity levels, creating an environment that is unfavorable for the growth of certain microorganisms.
This is particularly important in canned and pickled foods where acidity plays a crucial role in preventing the growth of harmful bacteria like Clostridium botulinum.

Moreover, Acetic acid also contributes to the preservation of additives foods by enhancing flavor.
Acetic acid adds a characteristic tartness or sourness, which can improve the taste profile of various products.
By enhancing the overall sensory experience, Acetic acid can help prolong the consumer acceptability and consumption of additives foods.

In summary, Acetic acid plays a vital role in preserving additives foods by acting as an antimicrobial agent, pH regulator, and flavor enhancer.
Acetic acid's usage ensures the safety and prolonged shelf life of various food products.
In conclusion, Acetic acid plays a crucial role as an additive in the food industry.

With its versatile properties, Acetic acid enhances flavors and acts as a natural preservative, increasing the shelf life of various food products.
Despite some concerns about its safety and potential health effects, research suggests that when consumed in moderation, Acetic acid is generally considered safe for consumption.

As consumers, it is important to stay informed about the presence of Acetic acid in our food products and make informed choices.
So, next time you come across the ingredient label with Acetic acid, rest assured that it can be embraced as a safe and effective addition to additive foods.



PROPERTIES OF ACETIC ACID:
-Acetic acid crystals:

*Acidity
The hydrogen centre in the carboxyl group (−COOH) in carboxylic acids such as acetic acid can separate from the molecule by ionization:
CH3COOH ⇌ CH3CO−2 + H+

Because of this release of the proton (H+), acetic acid has acidic character.
Acetic acid is a weak monoprotic acid.
In aqueous solution, Acetic Acid has a pKa value of 4.76.

Acetic Acid's conjugate base is acetate (CH3COO−).
A 1.0 M solution (about the concentration of domestic vinegar) has a pH of 2.4, indicating that merely 0.4% of the acetic acid molecules are dissociated.
Only in very dilute (< 10−6 M) solution, acetic acid is >90% dissociated.

*Deprotonation equilibrium of acetic acid in water
Cyclic dimer of acetic acid; dashed green lines represent hydrogen bonds



STRUCTURE OF ACETIC ACID:
In solid acetic acid, the molecules form chains of individual molecules interconnected by hydrogen bonds.
In the vapour phase at 120 °C (248 °F), dimers can be detected.

Dimers also occur in the liquid phase in dilute solutions with non-hydrogen-bonding solvents, and to a certain extent in pure acetic acid, but are disrupted by hydrogen-bonding solvents.

The dissociation enthalpy of the dimer is estimated at 65.0–66.0 kJ/mol, and the dissociation entropy at 154–157 J mol−1 K−1.
Other carboxylic acids engage in similar intermolecular hydrogen bonding interactions.



SOLVENT PROPERTIES OF ACETIC ACID:
Liquid acetic acid is a hydrophilic (polar) protic solvent, similar to ethanol and water.
With a relative static permittivity (dielectric constant) of 6.2, Acetic Acid dissolves not only polar compounds such as inorganic salts and sugars, but also non-polar compounds such as oils as well as polar solutes.

Acetic Acid is miscible with polar and non-polar solvents such as water, chloroform, and hexane.
With higher alkanes (starting with octane), acetic acid is not miscible at all compositions, and solubility of acetic acid in alkanes declines with longer n-alkanes.

The solvent and miscibility properties of acetic acid make it a useful industrial chemical, for example, as a solvent in the production of dimethyl terephthalate.



BIOCHEMISTRY OF ACETIC ACID:
At physiological pHs, acetic acid is usually fully ionised to acetate.
The acetyl group, formally derived from acetic acid, is fundamental to all forms of life.
Typically, Acetic Acid is bound to coenzyme A by acetyl-CoA synthetase enzymes, where it is central to the metabolism of carbohydrates and fats.

Unlike longer-chain carboxylic acids (the fatty acids), acetic acid does not occur in natural triglycerides.
Most of the aceate generated in cells for use in acetyl-CoA is synthesized directly from ethanol or pyruvate.
However, the artificial triglyceride triacetin (glycerine triacetate) is a common food additive and is found in cosmetics and topical medicines; this additive is metabolized to glycerol and acetic acid in the body.

Acetic acid is produced and excreted by acetic acid bacteria, notably the genus Acetobacter and Clostridium acetobutylicum.
These bacteria are found universally in foodstuffs, water, and soil, and acetic acid is produced naturally as fruits and other foods spoil.
Acetic acid is also a component of the vaginal lubrication of humans and other primates, where it appears to serve as a mild antibacterial agent.



PRODUCTION OF ACETIC ACID:
Acetic acid is produced industrially both synthetically and by bacterial fermentation.
About 75% of acetic acid made for use in the chemical industry is made by the carbonylation of methanol, explained below.

The biological route accounts for only about 10% of world production, but Acetic Acid remains important for the production of vinegar because many food purity laws require vinegar used in foods to be of biological origin.
Other processes are methyl formate isomerization, conversion of syngas to acetic acid, and gas phase oxidation of ethylene and ethanol.

Acetic acid can be purified via fractional freezing using an ice bath.
The water and other impurities will remain liquid while the acetic acid will precipitate out.
As of 2003–2005, total worldwide production of virgin acetic acid was estimated at 5 Mt/a (million tonnes per year), approximately half of which was produced in the United States.

European production was approximately 1 Mt/a and declining, while Japanese production was 0.7 Mt/a.
Another 1.5 Mt were recycled each year, bringing the total world market to 6.5 Mt/a.
Since then, the global production has increased from 10.7 Mt/a in 2010 to 17.88 Mt/a in 2023.


*Methanol carbonylation:
Most acetic acid is produced by methanol carbonylation.
In this process, methanol and carbon monoxide react to produce acetic acid according to the equation:
The process involves iodomethane as an intermediate, and occurs in three steps.
A metal carbonyl catalyst is needed for the carbonylation (step 2).

CH3OH + HI → CH3I + H2O
CH3I + CO → CH3COI
CH3COI + H2O → CH3COOH + HI

Two related processes exist for the carbonylation of methanol: the rhodium-catalyzed Monsanto process, and the iridium-catalyzed Cativa process.
The latter process is greener and more efficient and has largely supplanted the former process.

Catalytic amounts of water are used in both processes, but the Cativa process requires less, so the water-gas shift reaction is suppressed, and fewer by-products are formed.
By altering the process conditions, acetic anhydride may also be produced in plants using rhodium catalysis.


*Acetaldehyde oxidation:
Prior to the commercialization of the Monsanto process, most acetic acid was produced by oxidation of acetaldehyde.
This remains the second-most-important manufacturing method, although Acetic Acid is usually not competitive with the carbonylation of methanol.

The acetaldehyde can be produced by hydration of acetylene.
This was the dominant technology in the early 1900s.

Light naphtha components are readily oxidized by oxygen or even air to give peroxides, which decompose to produce acetic acid according to the chemical equation, illustrated with butane:

2 C4H10 + 5 O2 → 4 CH3CO2H + 2 H2O
Such oxidations require metal catalyst, such as the naphthenate salts of manganese, cobalt, and chromium.

The typical reaction is conducted at temperatures and pressures designed to be as hot as possible while still keeping the butane a liquid.
Typical reaction conditions are 150 °C (302 °F) and 55 atm.
Side-products may also form, including butanone, ethyl acetate, formic acid, and propionic acid.

These side-products are also commercially valuable, and the reaction conditions may be altered to produce more of them where needed.
However, the separation of acetic acid from these by-products adds to the cost of the process.
Similar conditions and catalysts are used for butane oxidation, the oxygen in air to produce acetic acid can oxidize acetaldehyde.

2 CH3CHO + O2 → 2 CH3CO2H
Using modern catalysts, this reaction can have an acetic acid yield greater than 95%.
The major side-products are ethyl acetate, formic acid, and formaldehyde, all of which have lower boiling points than acetic acid and are readily separated by distillation.


*Ethylene oxidation
Acetaldehyde may be prepared from ethylene via the Wacker process, and then oxidised as above.
In more recent times, chemical company Showa Denko, which opened an ethylene oxidation plant in Ōita, Japan, in 1997, commercialised a cheaper single-stage conversion of ethylene to acetic acid.

The process is catalyzed by a palladium metal catalyst supported on a heteropoly acid such as silicotungstic acid.
A similar process uses the same metal catalyst on silicotungstic acid and silica:

C2H4 + O2 → CH3CO2H
It is thought to be competitive with methanol carbonylation for smaller plants (100–250 kt/a), depending on the local price of ethylene.


*Oxidative fermentation:
For most of human history, acetic acid bacteria of the genus Acetobacter have made acetic acid, in the form of vinegar.
Given sufficient oxygen, these bacteria can produce vinegar from a variety of alcoholic foodstuffs.

Commonly used feeds include apple cider, wine, and fermented grain, malt, rice, or potato mashes.
The overall chemical reaction facilitated by these bacteria is:

C2H5OH + O2 → CH3COOH + H2O
A dilute alcohol solution inoculated with Acetobacter and kept in a warm, airy place will become vinegar over the course of a few months.
Industrial vinegar-making methods accelerate this process by improving the supply of oxygen to the bacteria.

The first batches of vinegar produced by fermentation probably followed errors in the winemaking process.
If must is fermented at too high a temperature, acetobacter will overwhelm the yeast naturally occurring on the grapes.

As the demand for vinegar for culinary, medical, and sanitary purposes increased, vintners quickly learned to use other organic materials to produce vinegar in the hot summer months before the grapes were ripe and ready for processing into wine.
This method was slow, however, and not always successful, as the vintners did not understand the process.

One of the first modern commercial processes was the "fast method" or "German method", first practised in Germany in 1823.
In this process, fermentation takes place in a tower packed with wood shavings or charcoal.

The alcohol-containing feed is trickled into the top of the tower, and fresh air supplied from the bottom by either natural or forced convection.
The improved air supply in this process cut the time to prepare vinegar from months to weeks.

Nowadays, most vinegar is made in submerged tank culture, first described in 1949 by Otto Hromatka and Heinrich Ebner.
In this method, alcohol is fermented to vinegar in a continuously stirred tank, and oxygen is supplied by bubbling air through the solution.
Using modern applications of this method, vinegar of 15% acetic acid can be prepared in only 24 hours in batch process, even 20% in 60-hour fed-batch process.


*Anaerobic fermentation:
Species of anaerobic bacteria, including members of the genus Clostridium or Acetobacterium, can convert sugars to acetic acid directly without creating ethanol as an intermediate.
The overall chemical reaction conducted by these bacteria may be represented as:

C6H12O6 → 3 CH3COOH
These acetogenic bacteria produce acetic acid from one-carbon compounds, including methanol, carbon monoxide, or a mixture of carbon dioxide and hydrogen:

2 CO2 + 4 H2 → CH3COOH + 2 H2O
This ability of Clostridium to metabolize sugars directly, or to produce acetic acid from less costly inputs, suggests that these bacteria could produce acetic acid more efficiently than ethanol-oxidizers like Acetobacter.

However, Clostridium bacteria are less acid-tolerant than Acetobacter.
Even the most acid-tolerant Clostridium strains can produce vinegar in concentrations of only a few per cent, compared to Acetobacter strains that can produce vinegar in concentrations up to 20%.

At present, it remains more cost-effective to produce vinegar using Acetobacter, rather than using Clostridium and concentrating it.
As a result, although acetogenic bacteria have been known since 1940, their industrial use is confined to a few niche applications.



REACTIONS OF ACETIC ACID:
Acetic acid undergoes the typical chemical reactions of a carboxylic acid.
Upon treatment with a standard base, Acetic Acid converts to metal acetate and water.
With strong bases (e.g., organolithium reagents), Acetic Acid can be doubly deprotonated to give LiCH2COOLi.

Reduction of acetic acid gives ethanol.
The OH group is the main site of reaction, as illustrated by the conversion of acetic acid to acetyl chloride.
Other substitution derivatives include acetic anhydride; this anhydride is produced by loss of water from two molecules of acetic acid.

Esters of acetic acid can likewise be formed via Fischer esterification, and amides can be formed.
When heated above 440 °C (824 °F), acetic acid decomposes to produce carbon dioxide and methane, or to produce ketene and water:
CH3COOH → CH4 + CO2
CH3COOH → CH2=C=O + H2O



REACTIONS WITH INORGANIC COMPOUNDS OF ACETIC ACID:
Acetic acid is mildly corrosive to metals including iron, magnesium, and zinc, forming hydrogen gas and salts called acetates:
Mg + 2 CH3COOH → (CH3COO)2Mg + H2

Because aluminium forms a passivating acid-resistant film of aluminium oxide, aluminium tanks are used to transport acetic acid.
Containers lined with glass, stainless steel or polyethylene are also used for this purpose.
Metal acetates can also be prepared from acetic acid and an appropriate base, as in the popular "baking soda + vinegar" reaction giving off sodium acetate:

NaHCO3 + CH3COOH → CH3COONa + CO2 + H2O
A colour reaction for salts of acetic acid is iron(III) chloride solution, which results in a deeply red colour that disappears after acidification.
A more sensitive test uses lanthanum nitrate with iodine and ammonia to give a blue solution.
Acetates when heated with arsenic trioxide form cacodyl oxide, which can be detected by its malodorous vapours.



OTHER DERIVATIVES OF ACETIC ACID:
Organic or inorganic salts are produced from acetic acid.
Some commercially significant derivatives:
Sodium acetate, used in the textile industry and as a food preservative (E262).

Copper(II) acetate, used as a pigment and a fungicide.
Aluminium acetate and iron(II) acetate—used as mordants for dyes.
Palladium(II) acetate, used as a catalyst for organic coupling reactions such as the Heck reaction.

Halogenated acetic acids are produced from acetic acid.
Some commercially significant derivatives:
Chloroacetic acid (monochloroacetic acid, MCA), dichloroacetic acid (considered a by-product), and trichloroacetic acid.

MCA is used in the manufacture of indigo dye.
Bromoacetic acid, which is esterified to produce the reagent ethyl bromoacetate.
Trifluoroacetic acid, which is a common reagent in organic synthesis.
Amounts of acetic acid used in these other applications together account for another 5–10% of acetic acid use worldwide



STRUCTURE OF ACETIC ACID:
It can be observed in the solid-state of acetic acid that there is a chain of molecules wherein individual molecules are connected to each other via hydrogen bonds.
Dimers of ethanoic acid in Acetic Acid's vapour phase can be found at temperatures approximating to 120o

Even in the liquid phase of ethanoic acid, Acetic Acid's dimers can be found when it is present in a dilute solution.
These dimers are adversely affected by solvents that promote hydrogen bonding.

The structure of acetic acid is given by CH3(C=O)OH, or CH3CO2H
Structurally, Acetic Acid is the second simplest carboxylic acid (the simplest being formic acid, HCOOH), and is essentially a methyl group with a carboxyl functional group attached to it.



PREPARATION OF ACETIC ACID:
Acetic acid is produced industrially via the carbonylation of methanol.
The chemical equations for the three steps involved in this process are provided below.
CH3OH (methanol) + HI (hydrogen iodide) → CH3I (methyl iodide intermediate) + H2O

CH3I + CO (carbon monoxide) → CH3COI (acetyl iodide)
CH3COI + H2O → CH3COOH (acetic acid) + HI

Here, a methyl iodide intermediate is generated from the reaction between methanol and hydrogen iodide.
This intermediate is then reacted with carbon monoxide and the resulting compound is treated with water to afford the acetic acid product.
It is important to note that a metal carbonyl complex must be used as a catalyst for step 2 of this process.



OTHER METHODS OF PREPARING ACETIC ACID:
Some naphthalene salts of cobalt, chromium, and manganese can be employed as metal catalysts in the oxidation of acetaldehyde.
The chemical equation for this reaction can be written as:
O2 + 2CH3CHO → 2CH3COOH

Ethylene (C2H4) can be oxidized into acetic acid with the help of a palladium catalyst and a heteropoly acid, as described by the following chemical reaction.
O2 + C2H4 → CH3COOH

Some anaerobic bacteria have the ability to directly convert sugar into acetic acid.
C6H12O6 → 3CH3COOH
It can be noted that no ethanol intermediates are formed in the anaerobic fermentation of sugar by these bacteria.



PHYSICAL PROEPRTIES OF ACETIC ACID:
Even though ethanoic acid is considered to be a weak acid, in its concentrated form, it possesses strong corrosive powers and can even attack the human skin if exposed to it.
Some general properties of acetic acid are listed below.

Ethanoic acid appears to be a colourless liquid and has a pungent smell.
At STP, the melting and boiling points of ethanoic acid are 289K and 391K respectively.
The molar mass of acetic acid is 60.052 g/mol and its density in the liquid form is 1.049 g.cm-3.

The carboxyl functional group in ethanoic acid can cause ionization of the compound, given by the reaction: CH3COOH ⇌ CH3COO– + H+
The release of the proton, described by the equilibrium reaction above, is the root cause of the acidic quality of acetic acid.
The acid dissociation constant (pKa) of ethanoic acid in a solution of water is 4.76.

The conjugate base of acetic acid is acetate, given by CH3COO–.
The pH of an ethanoic acid solution of 1.0M concentration is 2.4, which implies that it does not dissociate completely.
In its liquid form, acetic acid is a polar, protic solvent, with a dielectric constant of 6.2.

The metabolism of carbohydrates and fats in many animals is centered around the binding of acetic acid to coenzyme A.
Generally, this compound is produced via the reaction between methanol and carbon monoxide (carbonylation of methanol).



CHEMICAL PROPERTIES OF ACETIC ACID:
The chemical reactions undergone by acetic acid are similar to those of other carboxylic acids.
When heated to temperatures above 440oC, this compound undergoes decomposition to yield either methane and carbon dioxide or water and ethenone, as described by the following chemical equations.

CH3COOH + Heat → CO2 + CH4
CH3COOH + Heat → H2C=C=O + H2O
Some metals such as magnesium, zinc, and iron undergo corrosion when exposed to acetic acid.
These reactions result in the formation of acetate salts.

2CH3COOH + Mg → Mg(CH3COO)2 (magnesium acetate) + H2
The reaction between ethanoic acid and magnesium results in the formation of magnesium acetate and hydrogen gas, as described by the chemical equation provided above.



OTHER REACTIONS OF ACETIC ACID:
Acetic acid reacts with alkalis and forms acetate salts, as described below.
CH3COOH + KOH → CH3COOK + H2O
This compound also forms acetate salts by reacting with carbonates (along with carbon dioxide and water).
Examples of such reactions include:

2CH3COOH + Na2CO3 (sodium carbonate) → 2CH3COONa + CO2 + H2O
CH3COOH + NaHCO3 (sodium bicarbonate) → CH3COONa + CO2 + H2O
The reaction between PCl5 and ethanoic acid results in the formation of ethanoyl chloride.



WHAT ARE NATURAL SOURCES OF ACETIC ACID?
Acetates (salts of acetic acid) are common constituents of animal and plant tissues and are formed during the metabolism of food substances.
Acetate is readily metabolized by most tissues and may give rise to the production of ketones as intermediates.
Acetate is used by the body as a building block to make phospholipids, neutral lipids, steroids, sterols, and saturated and unsaturated fatty acids in a variety of human and animal tissue preparations.



KEY POINTS/OVERVIEW OF ACETIC ACID:
One of the most common ways consumers may come into contact with acetic acid is in the form of household vinegar, which generally contains about 5 percent acetic acid and 95 percent water.

When acetic acid is at 99.5 percent concentration, it is referred to a glacial acetic acid, which can be used as raw material and solvent in the production of other chemical products.

Industrial applications of glacial acetic acid include producing vinyl acetate, as solvent to dissolve oils, sulfur and iodine; acidizing oil and gas; manufacturing pharmaceuticals and vitamins, and food processing.



HOW ACETIC ACID GETS INTO THE ENVIRONMENT:
Acetic acid can enter the environment from discharge and emissions from industries.
The burning of plastics or rubber, and exhaust fumes from vehicles may also release acetic acid into the environment.
When released into soil Acetic Acid evaporates into the air where it is broken down naturally by sunlight.
Levels of acetic acid in the environment would be expected to be low.



PROPERTIES OF ACETIC ACID:
Acetic acid is a smooth, colourless liquid with a 1 ppm visible, poisonous and destructive, unpleasant vinegar odour.
The melting point of Acetic Acid is 16.73 ° C and the usual 117.9 ° C boiling point.
At 20°C, the density of pure acetic acid is 1.0491.

It is highly hygroscopic acetic acid.
It is possible to link the purity of the water solutions to their freezing point.
In carboxylic acids such as acetic acid, the hydrogen centre in the carboxyl group −COOH can differentiate from the molecule by ionization:

Due to this proton H+1 release, acetic acid has an acidic character.
Acetic acid is a weak monoprotic acid.
Acetic Acid has a pK value of 4.76 in an aqueous solution.

Acetate CH3COO−1 is the conjugate base.
For polar and non-polar solvents such as acid, chloroform, and hexane, Acetic Acid is miscible.
The molecules form chains in solid acetic acid, with hydrogen bonds interconnecting individual molecules.

Dimers can be found in the vapour at 120 °C.
In the liquid form, dimers often exist in dilute solutions in non-hydrogen-bonding solvents and, to a certain degree, in pure acetic acid; but are interacted with by solvents that bind to hydrogen.

Acetic acid is normally completely ionized to acetate at physiological phis.
Acetic Acid is central to the metabolism of carbohydrates and fats when bound to coenzyme A.
Acetic acid does not exist in natural triglycerides, unlike longer-chain carboxylic acids (fatty acids).



DEHYDRATION OF ACETIC ACID:
Dehydration of acetic acid is one of the most important industrial uses of AD in the manufacture of aromatic acids such as terephthalic acid (TA), which involves a high purity of acetic acid.

Two major parts are used in the manufacturing process: oxidation (where p-xylene is catalytically oxidized to produce crude TA) and PTA purification.
Acetic acid, present as a solvent in the oxidation reactor but also helpful to the reaction itself, must be isolated from the oxidation-produced water.

For the effective and economical operation of a TA facility, the recovery and storage of the acetic acid solvent are important.
At high water temperatures, water, and acetic acid show a pinch point, make recovering the pure acid very difficult.
Two absorbers (low and high pressure) and an acid dehydration column consist of a traditional acetic acid recovery unit in a PTA phase.

Tall columns of 70–80 trays require the separation of acetic acid and water by traditional distillation.
N-butyl acetate, which exhibits minimal miscibility with water and forms a heterogeneous azeotrope (b.p. 90.23°C), which is a typical azeotropic agent.
With all the water being fed to the dehydration column, n-Butyl acetate is added in appropriate amounts to form an azeotrope.

On condensation, the heterogeneous azeotrope forms two phases; an organic layer containing almost pure n-butyl acetate and an aqueous layer phase containing almost pure water.
The organic phase is recycled back to the column of dehydration, while the aqueous phase is fed to a column of stripping.
The amount of acetic acid lost in the aqueous discharge is cut by approximately 40 per cent as AD results in a cleaner separation.



PHYSICAL and CHEMICAL PROPERTIES of ACETIC ACID:
Molecular Weight: 60.05 g/mol
XLogP3-AA: -0.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 0
Exact Mass: 60.021129366 g/mol
Monoisotopic Mass: 60.021129366 g/mol
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 4
Formal Charge: 0
Complexity: 31
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1

Compound Is Canonicalized: Yes
Chemical formula: CH3COOH
Molar mass: 60.052 g·mol−1
Appearance: Colourless liquid
Odor: Heavily vinegar-like
Density: 1.049 g/cm3 (liquid); 1.27 g/cm3 (solid)
Melting point: 16 to 17 °C; 61 to 62 °F; 289 to 290 K
Boiling point: 118 to 119 °C; 244 to 246 °F; 391 to 392 K
Solubility in water: Miscible
log P: -0.28
Vapor pressure: 1.54653947 kPa (20 °C); 11.6 mmHg (20 °C)
Acidity (pKa): 4.756
Conjugate base: Acetate
Magnetic susceptibility (χ): -31.54·10−6 cm3/mol
Refractive index (nD): 1.371 (VD = 18.19)
Viscosity: 1.22 mPa s; 1.22 cP
Dipole moment: 1.74 D

Thermochemistry
Heat capacity (C): 123.1 J K−1 mol−1
Std molar entropy (S⦵298): 158.0 J K−1 mol−1
Std enthalpy of formation (ΔfH⦵298): -483.88–483.16 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): -875.50–874.82 kJ/mol
Physical state: Liquid
Color: Colorless
Odor: Stinging
Melting point/freezing point: Melting point/range: 16.2 °C - lit.
Initial boiling point and boiling range: 117 - 118 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: Upper explosion limit: 19.9% (V), Lower explosion limit: 4% (V)
Flash point: 39 °C - closed cup
Autoignition temperature: 463 °C
Decomposition temperature: Distillable in an undecomposed state at normal pressure.
pH: 2.5 at 50 g/L at 20 °C

Viscosity:
Kinematic viscosity: 1.17 mm2/s at 20 °C
Dynamic viscosity: 1.05 mPa·s at 25 °C
Water solubility: 602.9 g/L at 25 °C at 1.013 hPa - completely soluble
Partition coefficient (n-octanol/water): log Pow: -0.17 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: 20.79 hPa at 25 °C
Density: 1.049 g/cm3 at 25 °C - lit.
Relative vapor density: 2.07
Surface tension: 28.8 mN/m at 10.0 °C
CAS number: 64-19-7
Molecular formula: C2H4O2
Molecular weight: 60.052 g/mol
Density: 1.1 ± 0.1 g/cm3
Boiling point: 117.1 ± 3.0 °C at 760 mmHg
Melting point: 16.2 °C (lit.)
Flash point: 40.0 ± 0.0 °C

EC index number: 607-002-00-6
EC number: 200-580-7
Hill Formula: C₂H₄O₂
Chemical formula: CH₃COOH
Molar Mass: 60.05 g/mol
HS Code: 2915 21 00
Boiling point: 116 - 118 °C (1013 hPa)
Density: 1.04 g/cm3 (25 °C)
Explosion limit: 4 - 19.9% (V)
Flash point: 39 °C
Ignition temperature: 485 °C
Melting Point: 16.64 °C
pH value: 2.5 (50 g/L, H₂O, 20 °C)
Vapor pressure: 20.79 hPa (25 °C)
Viscosity kinematic: 1.17 mm2/s (20 °C)

Solubility: 602.9 g/L soluble
Boiling point: 244°F
Molecular weight: 60.1
Freezing point/melting point: 62°F
Vapor pressure: 11 mmHg
Flash point: 103°F
Specific gravity: 1.05
Ionization potential: 10.66 eV
Lower explosive limit (LEL): 4.0%
Upper explosive limit (UEL): 19.9% at 200°F
NFPA health rating: 3
NFPA fire rating: 2
NFPA reactivity rating: 0
Alternative CAS RN: -
MDL Number: MFCD00036152
Storage Temperature: +20°C



FIRST AID MEASURES of ACETIC ACID:
-Description of first-aid measures:
*General advice:
First aiders need to protect themselves.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water.
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of ACETIC ACID:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up with liquid-absorbent and neutralising material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ACETIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ACETIC ACID:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: butyl-rubber
Minimum layer thickness: 0,7 mm
Break through time: 480 min
Splash contact:
Material: Latex gloves
Minimum layer thickness: 0,6 mm
Break through time: 30 min
*Body Protection:
Flame retardant antistatic protective clothing.
*Respiratory protection:
Recommended Filter type: filter E-(P2)
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ACETIC ACID:
-Precautions for safe handling:
*Advice on protection against fire and explosion:
Take precautionary measures against static discharge.
*Hygiene measures:
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities
*Storage conditions:
Keep container tightly closed in a dry and well-ventilated place.
Moisture sensitive.



STABILITY and REACTIVITY of ACETIC ACID:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Incompatible materials:
No data available

ACETIC ACID %80-%100
Ethylic acid; Methanecarboxylic acid; vinegar; Vinegar acid; Acetic acid, glacial; Essigsäure; ácido acético; Acide acétique; Ethanoic acid; Acetasol; Octowy kwas; Kyselina octova; Essigsaeure; Octowy kwas; Vosol CAS NO:64-19-7
ACETIC ACID 80%
Acetic Acid 80% is completely soluble in water.
Acetic Acid 80% is a chemical reagent for the production of chemicals.


CAS Number: 64-19-7
EC Number: 200-580-7
E number: E260 (preservatives)
Molecular Formula: C2H4O2 / CH3COOH



SYNONYMS:
Acetic acid, Ethanoic acid, Vinegar (when dilute), Hydrogen acetate, Methanecarboxylic acid, Ethylic acid, Ethanoic acid, Ethylic acid, Glacial acetic acid, Methanecarboxylic acid, Vinegar acid, CH3COOH, Acetasol, Acide acetique, Acido acetico, Azijnzuur, Essigsaeure, Octowy kwas, Acetic acid, glacial, Kyselina octova, UN 2789, Aci-jel, Shotgun, Ethanoic acid monomer, NSC 132953, Ethanoic acid, vinegar, ethylic acid, vinegar acid, methanecarboxylic acid, TCLP extraction fluid 2, shotgun, glacial acetic acid, glacial ethanoic acid, Ethanoic acid, Ethylic acid, Glacial acetic acid, Methanecarboxylic acid, Vinegar acid, CH3COOH, Acetasol, Acide acetique, Acido acetico, Azijnzuur, Essigsaeure, Octowy kwas, Acetic acid, glacial, Kyselina octova, UN 2789, Aci-jel, Shotgun, Ethanoic acid monomer, NSC 132953, BDBM50074329, FA 2:0, LMFA01010002, NSC132953, NSC406306, Acetic acid for HPLC >=99.8%, AKOS000268789, ACIDUM ACETICUM [WHO-IP LATIN], DB03166, UN 2789, Acetic acid >=99.5% FCC FG, Acetic acid natural >=99.5% FG, Acetic acid ReagentPlus(R) >=99%, CAS-64-19-7, USEPA/OPP Pesticide Code: 044001, Acetic acid USP 99.5-100.5%, NCGC00255303-01, Acetic acid 1000 microg/mL in Methanol, Acetic acid SAJ first grade >=99.0%, Acetic acid 1000 microg/mL in Acetonitrile, Acetic acid >=99.99% trace metals basis, Acetic acid JIS special grade >=99.7%, Acetic acid purified by double-distillation, NS00002089, Acetic acid UV HPLC spectroscopic 99.9%, EN300-18074, Acetic acid Vetec(TM) reagent grade >=99%, Bifido Selective Supplement B for microbiology, C00033, D00010, ORLEX HC COMPONENT ACETIC ACID GLACIAL, Q47512, VOSOL HC COMPONENT ACETIC ACID GLACIAL, Acetic acid glacial electronic grade 99.7%, TRIDESILON COMPONENT ACETIC ACID GLACIAL, A834671, ACETASOL HC COMPONENT ACETIC ACID GLACIAL, Acetic acid >=99.7% SAJ super special grade, ACETIC ACID GLACIAL COMPONENT OF BOROFAIR, ACETIC ACID GLACIAL COMPONENT OF ORLEX HC, ACETIC ACID GLACIAL COMPONENT OF VOSOL HC, SR-01000944354, ACETIC ACID GLACIAL COMPONENT OF TRIDESILON, SR-01000944354-1, ACETIC ACID GLACIAL COMPONENT OF ACETASOL HC, Glacial acetic acid meets USP testing specifications, InChI=1/C2H4O2/c1-2(3)4/h1H3(H,3,4), Acetic acid >=99.7% suitable for amino acid analysis, Acetic acid >=99.7% for titration in non-aqueous medium, Acetic acid for luminescence BioUltra >=99.5% GC, Acetic acid p.a. ACS reagent reag. ISO reag. Ph. Eur. 99.8%, Acetic acid semiconductor grade MOS PURANAL(TM) Honeywell 17926, Glacial acetic acid United States Pharmacopeia USP Reference Standard, Acetic acid puriss. p.a. ACS reagent reag. ISO reag. Ph. Eur. >=99.8%, Glacial Acetic Acid Pharmaceutical Secondary Standard Certified Reference Material, Acetic acid puriss. meets analytical specification of Ph. Eur. BP USP FCC 99.8-100.5%, acetic-acid, Glacial acetate, acetic cid, actic acid, UNII-Q40Q9N063P, acetic -acid, Distilled vinegar, Methanecarboxylate, Acetic acid glacial [USP:JAN], Acetasol (TN), Acetic acid glacial for LC-MS, Vinegar (Salt/Mix), HOOCCH3, 546-67-8, Acetic acid LC/MS Grade, ACETIC ACID [II], ACETIC ACID [MI], Acetic acid ACS reagent, bmse000191, bmse000817, bmse000857, Otic Domeboro (Salt/Mix), EC 200-580-7, Acetic acid (JP17/NF), ACETIC ACID [FHFI], ACETIC ACID [INCI], Acetic Acid [for LC-MS], ACETIC ACID [VANDF], NCIOpen2_000659, NCIOpen2_000682, Acetic acid glacial (USP), 4-02-00-00094 (Beilstein Handbook Reference), 77671-22-8, Glacial acetic acid (JP17), UN 2790 (Salt/Mix), ACETIC ACID [WHO-DD], ACETIC ACID [WHO-IP], ACETICUM ACIDUM [HPUS], GTPL1058, Acetic Acid Glacial HPLC Grade, Acetic acid analytical standard, Acetic acid Glacial USP grade, Acetic acid puriss. >=80%, Acetic acid 99.8% anhydrous, Acetic acid AR >=99.8%, Acetic acid LR >=99.5%, Acetic acid extra pure 99.8%, Acetic acid 99.5-100.0%, Acetic acid Glacial ACS Reagent, STR00276, Acetic acid puriss. 99-100%, Tox21_301453, Acetic acid glacial >=99.85%, acetic acid, ethanoic acid, 64-19-7, Ethylic acid, Vinegar acid, Acetic acid glacial, Glacial acetic acid, Acetic acid glacial, Methanecarboxylic acid, Acetasol, Essigsaeure, Acide acetique, Pyroligneous acid, Vinegar, Azijnzuur, Aceticum acidum, Acido acetico, Octowy kwas, Aci-jel, HOAc, ethoic acid, Kyselina octova, Orthoacetic acid, AcOH, Ethanoic acid monomer, Acetic, Caswell No. 003, Otic Tridesilon, MeCOOH, Acetic acid-17O2, Otic Domeboro, Acidum aceticum glaciale, Acidum aceticum, CH3-COOH, acetic acid-, CH3CO2H, UN2789, UN2790, EPA Pesticide Chemical Code 044001, NSC 132953, NSC-132953, NSC-406306, BRN 0506007, Acetic acid diluted, INS NO.260, Acetic acid [JAN], DTXSID5024394, MeCO2H, CHEBI:15366, AI3-02394, CH3COOH, INS-260, Q40Q9N063P, E-260, 10.Methanecarboxylic acid, CHEMBL539, NSC-111201, NSC-112209, NSC-115870, NSC-127175, Acetic acid-2-13C,d4, INS No. 260, DTXCID304394, E 260, Acetic-13C2 acid (8CI,9CI), Ethanoat, Shotgun, MFCD00036152, Acetic acid of a concentration of more than 10 per cent by weight of acetic acid, 285977-76-6, 68475-71-8, C2:0, acetyl alcohol, Orlex, Vosol, ACETIC-1-13C-2-D3 ACID-1 H (D), WLN: QV1, ACETIC ACID (MART.), ACETIC ACID [MART.], Acetic acid >=99.7%, 57745-60-5, 63459-47-2, FEMA Number 2006, ACETIC-13C2-2-D3 ACID, 97 ATOM % 13C, 97 ATOM % D, Acetic acid ACS reagent >=99.7%, ACY, HSDB 40, CCRIS 5952, 79562-15-5, methane carboxylic acid, EINECS 200-580-7, Acetic acid 0.25% in plastic container, Essigsaure, Ethylate, acetic acid, ethanoic acid, ethylic acid, acetic acid, glacial, methanecarboxylic acid, vinegar acid, glacial, acetasol, acide acetique, essigsaeure,



Acetic Acid 80% is an organic acid available in various standard strengths.
Pure Acetic Acid 80% is known as Acetic Acid 80% Glacial because it will freeze at moderate temperatures (16.6C).
Acetic Acid 80% is an organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).


Acetic Acid 80% is a colourless liquid which when undiluted is also called ‘glacial Acetic Acid 80%’.
Acetic Acid 80%, CH3COOH, also known as ethanoic acid, is an organic acid which has a pungent smell.
Acetic Acid 80% is a weak acid, in that it is only partially dissociated in an aqueous solution.


Acetic Acid 80% is hygroscopic (absorbs moisture from the air) and freezes at 16.5C to a colourless crystalline solid.
Acetic Acid 80% is one of the simplest carboxylic acids, and is a very important industrial chemical.
Acetic Acid 80% is produced by biological and synthetic ways in the industry.


The salt and Acetic Acid 80%'s ester are called acetate.
Acetic Acid 80% is completely soluble in water.
Acetic Acid 80% is a chemical reagent for the production of chemicals.


The most common one-time use of Acetic Acid 80% is for the production of vinyl acetate monomer as well as the production of acetic anhydride and esters.
Acetic Acid 80% is the main component of vinegar (apart from water; vinegar is roughly 8% Acetic Acid 80% by volume), and has a distinctive sour taste and pungent smell.


Acetic Acid 80% Food Grade is one of the simplest carboxylic acids.
Acetic Acid 80% is an important chemical reagent and industrial chemical, mainly used in the production of cellulose acetate for photographic film and polyvinyl acetate for wood glue, as well as synthetic fibres and fabrics.


Acetic Acid 80%, also known as ethanoic acid, is a colourless liquid and organic compound.
With the chemical formula CH₃COOH, Acetic Acid 80% is a chemical reagent for the production of chemicals.
Acetic Acid 80% has a CAS number of 64-19-7.
The amount of Acetic Acid 80% in vinegar is relatively small.


Acetic Acid 80%, otherwise known as ethanoic acid, is a simple carboxylic acid that usually forms a liquid at room temperature.
Acetic Acid 80% is most widely used in table vinegar due to the preservative properties it holds and is the chemical responsible for the characteristic vinegar odour.


Acetic Acid 80% also has a wide range of applications in the chemical industry and is used in the synthesis of esters and vinyl acetate. Within a laboratory setting, Acetic Acid 80% is a commonly used solvent.
Acetic Acid 80% is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 000 tonnes per annum.


Acetic Acid 80% is a product of the oxidation of ethanol and of the destructive distillation of wood.
Acetic Acid 80% is used locally, occasionally internally, as a counterirritant and also as a reagent.
Acetic Acid 80% otic (for the ear) is an antibiotic that treats infections caused by bacteria or fungus.


While this is usually the least expensive way of purchasing Acetic Acid 80% we find that more dilute grades such as 90% are more in demand to eliminate most of the solidification problems.
Acetic Acid 80% may sound like it should be in a chemistry lab or science fair rather than in your kitchen pantry.


However, Acetic Acid 80% is actually the main compound found in vinegar and is responsible for both its unique flavor and acidity.
Not only that, but Acetic Acid 80%’s also believed to contribute to many of the health benefits of apple cider vinegar due to its potent medicinal properties.
Acetic Acid 80%, also known as ethanoic acid, is a chemical compound found in many different products.


Acetic Acid 80%’s perhaps most well-known as the main component of vinegar, apart from water, and is thought to supply ingredients like apple cider vinegar with many of their health-promoting properties.
Chemically speaking, the Acetic Acid 80% formula is C2H4O2, which can also be written as CH3COOH or CH3CO2H.


Because of the presence of a carbon atom in the Acetic Acid 80% structure, it’s considered an organic compound.
The Acetic Acid 80% density is about 1.05 grams/cm³; compared to other compounds like nitric acid, sulfuric acid or formic acid, the density of Acetic Acid 80% is quite a bit lower.


Conversely, the Acetic Acid 80% melting point is significantly higher than many other acids, and the Acetic Acid 80% molar mass and Acetic Acid 80% boiling point tend to fall right about in the middle.
Acetic Acid 80% which is also known as methane carboxylic acid and ethanoic acid is basically a clear, colorless liquid, which has a strong and pungent smell.


Since Acetic Acid 80% has a carbon atom in its chemical formula, it is an organic compound and it comes with a chemical formula CH3COOH.
Interestingly, the word ‘acetic’ is derived from a Latin word called ‘acetum’ meaning ‘vinegar’.
Vinegar is the dilute form of Acetic Acid 80% and is the most common chemical substance among people.


Acetic Acid 80% is a main component of vinegar and also gives vinegar its characteristic smell.
Acetic Acid 80% (CH3COOH), also called ethanoic acid, is the most important of the carboxylic acids.
A dilute (approximately 5 percent by volume) solution of Acetic Acid 80% produced by fermentation and oxidation of natural carbohydrates is called vinegar; a salt, ester, or acylal of Acetic Acid 80% is called acetate.


Moving on, when Acetic Acid 80% or ethanoic acid is undiluted it is termed glacial Acetic Acid 80%.
Acetic Acid 80% is a weak acid but when it is in concentrated form, this acid is corrosive and can cause some damage to the skin.
Acetic Acid 80% appears as a clear colorless liquid with a strong odor of vinegar.


Flash point of Acetic Acid 80% is 104 °F.
Density of Acetic Acid 80% is 8.8 lb / gal.
Acetic Acid 80% is corrosive to metals and tissue.


Acetic Acid 80%, solution, more than 10% but not more than 80% acid appears as a colorless aqueous solution.
Acetic Acid 80% smells like vinegar.
Acetic Acid 80% is corrosive to metals and tissue.


Acetic Acid 80%, solution, more than 80% acid is a clear colorless aqueous solution with a pungent odor.
Acetic Acid 80% is faintly pink wet crystals with an odor of vinegar.
Acetic Acid 80% is a simple monocarboxylic acid containing two carbons.


Acetic Acid 80% has a role as a protic solvent, a food acidity regulator, an antimicrobial food preservative and a Daphnia magna metabolite.
Acetic Acid 80% is a conjugate acid of an acetate.
Acetic Acid 80% is a product of the oxidation of ethanol and of the destructive distillation of wood.


Acetic Acid 80% is a metabolite found in or produced by Escherichia coli.
Acetic Acid 80% is a natural product found in Camellia sinensis, Microchloropsis, and other organisms with data available.
Acetic Acid 80% is a synthetic carboxylic acid with antibacterial and antifungal properties.


Although its mechanism of action is not fully known, undissociated Acetic Acid 80% may enhance lipid solubility allowing increased fatty acid accumulation on the cell membrane or in other cell wall structures.
Acetic Acid 80% is one of the simplest carboxylic acids.


Acetic Acid 80% is an important chemical reagent and industrial chemical that is used in the production of plastic soft drink bottles, photographic film; and polyvinyl acetate for wood glue, as well as many synthetic fibres and fabrics.
Acetic Acid 80% can be very corrosive, depending on the concentration.


Acetic Acid 80% is one ingredient of cigarette.
The acetyl group, derived from Acetic Acid 80%, is fundamental to the biochemistry of virtually all forms of life.
When bound to coenzyme A it is central to the metabolism of carbohydrates and fats.


However, the concentration of free Acetic Acid 80% in cells is kept at a low level to avoid disrupting the control of the pH of the cell contents.
Acetic Acid 80% is produced and excreted by certain bacteria, notably the Acetobacter genus and Clostridium acetobutylicum.
These bacteria are found universally in foodstuffs, water, and soil, and Acetic Acid 80% is produced naturally as fruits and some other foods spoil.


Acetic Acid 80% is also a component of the vaginal lubrication of humans and other primates, where it appears to serve as a mild antibacterial agent.
Acetic Acid 80% /əˈsiːtɪk/, systematically named ethanoic acid /ˌɛθəˈnoʊɪk/, is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH (also written as CH3CO2H, C2H4O2, or HC2H3O2).


Vinegar is at least 4% Acetic Acid 80% by volume, making Acetic Acid 80% the main component of vinegar apart from water.
Acetic Acid 80% has been used, as a component of vinegar, throughout history from at least the third century BC.
Acetic Acid 80% is the second simplest carboxylic acid (after formic acid).


Acetic Acid 80% is an important chemical reagent and industrial chemical across various fields, used primarily in the production of cellulose acetate for photographic film, polyvinyl acetate for wood glue, and synthetic fibres and fabrics.
Acetic Acid 80% is a very important organic compound in the day-to-day lives of humans.


The desirable solvent properties of Acetic Acid 80%, along with its ability to form miscible mixtures with both polar and non-polar compounds, make it a very important industrial solvent.
Acetic Acid 80% is also known as ethanoic acid, ethylic acid, vinegar acid, and methane carboxylic acid.


Acetic Acid 80% is a byproduct of fermentation, and gives vinegar its characteristic odor.
Vinegar is about 4-6% Acetic Acid 80% in water.
More concentrated solutions can be found in laboratory use, and pure Acetic Acid 80% containing only traces of water is known as glacial Acetic Acid 80%.


Dilute solutions like vinegar can contact skin with no harm, but more concentrated solutions will burn the skin.
Glacial Acetic Acid 80% can cause skin burns and permanent eye damage, and will corrode metal.
Acetic Acid 80% is an organic compound with the formula CH3COOH.


Acetic Acid 80% is a carboxylic acid consisting of a methyl group that is attached to a carboxyl functional group.
The systematic IUPAC name of Acetic Acid 80% is ethanoic acid and its chemical formula can also be written as C2H4O2.
Vinegar is a solution of Acetic Acid 80% in water and contains between 5% to 20% ethanoic acid by volume.


The pungent smell and the sour taste are characteristic of the Acetic Acid 80% present in it.
An undiluted solution of Acetic Acid 80% is commonly referred to as glacial Acetic Acid 80%.
Acetic Acid 80% forms crystals which appear like ice at temperatures below 16.6oC.


Acetic Acid 80% (CH3COOH), the most important of the carboxylic acids.
A dilute (approximately 5 percent by volume) solution of Acetic Acid 80% produced by fermentation and oxidation of natural carbohydrates is called vinegar; a salt, ester, or acylal of Acetic Acid 80% is called acetate.


Industrially, Acetic Acid 80% is used in the preparation of metal acetates, used in some printing processes; vinyl acetate, employed in the production of plastics; cellulose acetate, used in making photographic films and textiles; and volatile organic esters (such as ethyl and butyl acetates), widely used as solvents for resins, paints, and lacquers.


Biologically, Acetic Acid 80% is an important metabolic intermediate, and it occurs naturally in body fluids and in plant juices.
Acetic Acid 80% has been prepared on an industrial scale by air oxidation of acetaldehyde, by oxidation of ethanol (ethyl alcohol), and by oxidation of butane and butene.


Today Acetic Acid 80% is manufactured by a process developed by the chemical company Monsanto in the 1960s; it involves a rhodium-iodine catalyzed carbonylation of methanol (methyl alcohol).
Pure Acetic Acid 80%, often called glacial Acetic Acid 80%, is a corrosive, colourless liquid (boiling point 117.9 °C [244.2 °F]; melting point 16.6 °C [61.9 °F]) that is completely miscible with water.


Acetic Acid 80% is a clear, colorless, organic liquid with a pungent odor similar to household vinegar.
Acetic Acid 80% or glacial Acetic Acid 80%, also known as ethanoic acid, is an organic compound with the chemical formula CH3COOH.
Pure glacial Acetic Acid 80% (anhydrous Acetic Acid 80%) is a colorless, hygroscopic liquid with a strong pungent odor.


The freezing point is 16.6°C, and Acetic Acid 80% turns into colorless crystals after solidification.
Acetic Acid 80% is an organic monobasic acid and can be miscible with water in any proportion.
Acetic Acid 80% is particularly corrosive to metals.


Acetic Acid 80% is widely found in nature, such as in the fermentation metabolism and putrefaction products of various glacial Acetic Acid 80% bacteria.
Acetic Acid 80% is also the main component of vinegar.
Moreover, glacial Acetic Acid 80% always plays an important role in many chemical reactions.


For example, Acetic Acid 80% can undergo displacement reactions with metals such as iron, zinc, and copper to generate metal acetates and hydrogen.
In addition, Acetic Acid 80% can react with alkalis, alkaline oxides, salts and certain metal oxides.
Acetic Acid 80% is an organic chemical substance, it is a colourless liquid with a very distinctive odour.


One of its most common uses is in the composition of vinegar, although Acetic Acid 80% is also used in cosmetics and pharmaceuticals, in the food, textile and chemical industries.
On an industrial level, Acetic Acid 80% is produced through the carbonylation of methanol and is used as a raw material for the production of different compounds.


Acetic Acid 80% can also be obtained through the food industry by the acetic fermentation process of ethanol, or more commonly explained, through alcoholic fermentation and with the distillation of wood.
Pure Acetic Acid 80% or glacial Acetic Acid 80%, also known as CH3COOH, is a liquid that can be harmful to our health due to its irritating and corrosive properties and can cause severe skin, eye and digestive tract irritation.


However, thanks to its combination with different substances, Acetic Acid 80% is possible to obtain everyday products that may be familiar to everyone, such as vinegar.
Vinegar is a hygroscopic substance, i.e. it can absorb moisture from its surroundings.


Therefore, when it is mixed with water, there is a very significant reduction in its volume.
On the other hand, when Acetic Acid 80% 100 % is exposed to low temperatures, the surface, also known as acetic essence, crystallises and forms ice-like crystals at the top.


Due to the chemical structure of Acetic Acid 80%, it has a very high boiling point.
Furthermore, it is worth noting that Acetic Acid 80%, being a carboxylic acid, has the ability to dissociate, but only slightly, as it is a weak acid [FC1].
Moreover, thanks to this ability to dissociate, Acetic Acid 80% conducts electricity effectively.


Acetic Acid 80% is an organic compound with the chemical formula CH3COOH.
Acetic Acid 80% is an organic monobasic acid and is the main component of vinegar.
Pure anhydrous Acetic Acid 80% (glacial Acetic Acid 80%) is a colorless, hygroscopic liquid with a freezing point of 16.6 ℃ (62 ℉).


After solidification, Acetic Acid 80% becomes a colorless crystal.
Acetic Acid 80% or ethanoic acid is a colourless liquid organic compound with the molecular formula CH3COOH.
When Acetic Acid 80% is dissolved in water, it is termed glacial Acetic Acid 80%.


Vinegar is no less than 4 per cent Acetic Acid 80% by volume, aside from water, allowing Acetic Acid 80% to be the main ingredient of vinegar.
Acetic Acid 80% is produced primarily as a precursor to polyvinyl acetate and cellulose acetate, in addition to household vinegar.
Acetic Acid 80% is a weak acid since the solution dissociates only slightly.


But concentrated Acetic Acid 80% is corrosive and can damage the flesh.
The second simplest carboxylic acid is Acetic Acid 80% (after formic acid).
Acetic Acid 80% consists of a methyl group to which a carboxyl group is bound.


Acetic Acid 80% is a colourless liquid organic compound with pungent characteristic odour.
Acetic Acid 80% is an acid that occurs naturally.
Acetic Acid 80% can also be produced synthetically either by acetylene or by using methanol.


Acetic Acid 80% is considered as a natural preservative for food products.
Acetic Acid 80% has been used for hundreds of years as a preservative (vinegar, French for "sour wine").
If during the fermentation of grapes or other fruits, oxygen is allowed into the container, then bacteria convert the ethanol present into Acetic Acid 80% causing the wine to turn sour.


Acetic Acid 80% may be synthetically produced using methanol carbonylation, acetaldehyde oxidation, or butane/naphtha oxidation.
Acetic Acid 80% is termed "glacial", and is completely miscible with water.
Acetic Acid 80% is the main component of vinegar.


Acetic Acid 80% appears as a clear, colorless liquid with a distinctive sour taste and pungent smell.
Acetic Acid 80% is used as a preservative, acidulant, and flavoring agent in mayonnaise and pickles.
Though Acetic Acid 80%’s considered safe, some are convinced it has potentially dangerous health effects.


Acetic Acid 80% systematically named ethanoic acid, is a colourless liquid organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).
When undiluted, Acetic Acid 80% is sometimes called glacial Acetic Acid 80%.


Acetic Acid 80% is an organic compound belonging to the weak carboxylic acids.
The set of properties of Acetic Acid 80% classifies it as a broad-spectrum reagent and allows it to be used in a wide variety of industrial fields: from pharmacology and cosmetology to the chemical and food industries.


Acetic Acid 80% is one of the most common acids used in the food industry and household.
Acetic Acid 80% is a colorless, pungent, odorless liquid that miscible mixes with water to form solutions of varying concentrations.
Due to its ability to crystallize at an already positive temperature, Acetic Acid 80% is also known as “glacial”.


Acetic Acid 80% is a synthetic carboxylic acid with antibacterial and antifungal properties.
Although Acetic Acid 80%'s mechanism of action is not fully known, undissociated Acetic Acid 80% may enhance lipid solubility allowing increased fatty acid accumulation on the cell membrane or in other cell wall structures.


Acetic Acid 80%, as a weak acid, can inhibit carbohydrate metabolism resulting in subsequent death of the organism.
Acetic Acid 80% is present in most fruits.
Acetic Acid 80% is produced by bacterial fermentation and thus present in all fermented products.


In mayonnaise, Acetic Acid 80% is added to increase the inactivation of Salmonella.
Acetic Acid 80%, known also as ethanoic acid, is a weak acid that is commonly used as a food preservative and flavoring agent.
Acetic Acid 80%'s chemical formula is CH3COOH, and its molecular weight is 60.05 g/mol.


Acetic Acid 80% is a clear, colorless liquid that has a pungent odor and a sour taste.
Acetic Acid 80% is miscible with water and most common organic solvents.
Acetic Acid 80% is produced naturally in most organisms as a byproduct of metabolism.


Acetic Acid 80% is also a major component of vinegar, which is a solution of Acetic Acid 80% and water that occurs naturally when ethanol in fermented fruit juices undergoes oxidation by Acetic Acid 80% bacteria.
The production of vinegar has been an ancient practice of food preservation and flavoring that dates back to ancient times.


Acetic Acid 80% has several applications outside of the food industry.
Acetic Acid 80% is used as a solvent in the production of various chemicals and is an important intermediate in the manufacture of polymers, fibers, and pharmaceuticals.


Acetic Acid 80% is classified as a weak acid because it only partially ionizes in water to produce hydrogen ions (H+) and acetate ions (CH3COO-).
The pH of a 1% solution of Acetic Acid 80% is approximately 2.4, which means it is acidic but relatively less acidic than some stronger acids like hydrochloric acid or sulfuric acid.


Acetic Acid 80% is both naturally occurring and synthetic.
Natural sources include fermentation and bacteria.
In fermentation, Acetic Acid 80% is produced when yeast breaks down sugar in the absence of oxygen.


Bacteria produce Acetic Acid 80% when they oxidize ethanol.
Synthetic Acetic Acid 80% is made by reacting methanol with carbon monoxide in the presence of a catalyst.
Acetic Acid 80% has a strong odor and taste.


The odor of Acetic Acid 80% is similar to that of vinegar and the taste is sour.
Acetic Acid 80% is not considered toxic in small quantities and is generally recognized as safe by the US Food and Drug Administration (FDA) when used in accordance with good manufacturing practices.


The safety of Acetic Acid 80% depends on its concentration, with higher concentrations being more corrosive to skin and eyes.
In summary, Acetic Acid 80% is a weak acid that is commonly used as a food preservative and flavoring agent.
Another important use of Acetic Acid 80% is as a chemical intermediate.


Lastly, Acetic Acid 80% is an important ingredient in the winemaking process.
In this case, Acetic Acid 80% is produced naturally as a byproduct of the wine fermentation process.
However, if Acetic Acid 80% levels are too high, it can cause a wine to taste or smell like vinegar, which is undesirable.


To avoid this, winemakers use sulfites to inhibit the growth of Acetic Acid 80% bacteria in the wine.
Acetic Acid 80% is also an effective cleaning agent, especially when it comes to eliminating stubborn stains or mineral build-up due to hard water.
Acetic Acid 80%'s acidic nature helps to loosen dirt, grime, and other impurities from surfaces.


Acetic Acid 80% is found naturally in many foods, including vinegar and fermented products.
However, when used as an additive, Acetic Acid 80% is typically produced synthetically.
Acetic Acid 80% is generally recognized as safe (GRAS) when used in accordance with good manufacturing practices.


Overall, Acetic Acid 80% is considered a safe food additive when used within recommended limits.
As with any food additive, Acetic Acid 80% is essential to follow regulations and guidelines set by relevant authorities.



USES and APPLICATIONS of ACETIC ACID 80%:
In the home, diluted Acetic Acid 80% is often used in descaling agents.
In the food industry, Acetic Acid 80% is used under the food additive (EU number E260) as an acidity regulator and as a condiment.
Acetic Acid 80% is widely approved for usage as a food additive.


Acetic Acid 80% 80% is an essential chemical with a wide range of applications.
Acetic Acid 80% is a strong organic acid, also known as ethanoic or vinegar acid, and is used in a variety of industries, from the production of paints and adhesives to the food and pharmaceutical industries.


Acetic Acid 80% is an efficient solvent and a condensing agent in chemical synthesis processes.
Acetic Acid 80% is also used in the production of vinyl acetate, a key ingredient in polymer manufacturing.
Acetic Acid 80% is a highly concentrated solution, ideal for professionals and experienced users.


With Acetic Acid 80% you can remove stubborn limescale, green deposits and other types of pollution.
In general, for most applications Acetic Acid 80% should first be diluted with water.
For a ready-made solution of Acetic Acid 80% that you can use immediately for your cleaning work, you can also purchase cleaning vinegar .


Acetic Acid 80% is most commonly used in the production of vinyl acetate monomer (VAM), in ester production and for the breeding of bees.
As a natural acid, Acetic Acid 80% offers a wide range of possible applications: e.g. in cleaning formulations and for decalcification.
In addition, Acetic Acid 80% is commonly used as a biogenic herbicide, although commercial use as a herbicide is not permitted on enclosed areas.


Applications of Acetic Acid 80%: Adhesives/sealants-B&C, Agriculture intermediates, Apparel, Architectural coatings, Automotive protective coatings, Building materials, Commercial printing inks, Construction chemicals, Decorative interiors, Fertilizer, Food ingredients, Food preservatives, Formulators, Hard surface care, Industrial cleaners, Institutional cleaners.


Applications of Acetic Acid 80%:Intermediates, Oil or gas processing, Other-food chemicals, Other-transportation, Packaging components non-food contact, Paints & coatings, Pharmaceutical chemicals, Process additives, Refining, Specialty chemicals, Starting material, and Water treatment industrial.


Acetic Acid 80% is a raw material used for the production of many downstream products.
For applications in drugs, foods, or feeds, Eastman provides Acetic Acid 80% in grades appropriate for these regulated uses.
Acetic Acid 80% is most commonly found in vinegar, which is used in recipes ranging from salad dressings to condiments, soups and sauces.


Vinegar is also used as a food preservative and pickling agent.
Plus, it can even be used to make natural cleaning products, skin toners, bug sprays and more.
Some medications contain Acetic Acid 80%, including those used to treat ear infections.


Some also use Acetic Acid 80% in the treatment of other conditions, including warts, lice and fungal infections, although more research is needed to evaluate its safety and effectiveness.
Acetic Acid 80% is also used by manufacturers to create a variety of different products.


In particular, Acetic Acid 80% is used to make chemical compounds like vinyl acetate monomer as well as perfumes, oral hygiene products, skin care products, inks and dyes.
Release to the environment of Acetic Acid 80% can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).


Other release to the environment of Acetic Acid 80% is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).


Acetic Acid 80% can be found in products with material based on: paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), leather (e.g. gloves, shoes, purses, furniture), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys) and wood (e.g. floors, furniture, toys).


Acetic Acid 80% is used in the following products: laboratory chemicals, pH regulators and water treatment products, water treatment chemicals, plant protection products and washing & cleaning products.
Acetic Acid 80% is used in the following areas: formulation of mixtures and/or re-packaging.


Acetic Acid 80% is used for the manufacture of: chemicals.
Other release to the environment of Acetic Acid 80% is likely to occur from: outdoor use and indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).


Acetic Acid 80% is used in the following products: coating products, perfumes and fragrances, paper chemicals and dyes, textile treatment products and dyes, metal surface treatment products, non-metal-surface treatment products and polymers.
Acetic Acid 80% is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Release to the environment of Acetic Acid 80% can occur from industrial use: formulation of mixtures, formulation in materials, manufacturing of the substance, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, for thermoplastic manufacture, as processing aid, of substances in closed systems with minimal release and in the production of articles.


Acetic Acid 80% is used in the following products: laboratory chemicals, pH regulators and water treatment products, oil and gas exploration or production products, water treatment chemicals, washing & cleaning products, polymers and coating products.
Acetic Acid 80% is used in the following areas: mining and formulation of mixtures and/or re-packaging.


Acetic Acid 80% is used for the manufacture of: chemicals, textile, leather or fur, wood and wood products and pulp, paper and paper products.
Release to the environment of Acetic Acid 80% can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and manufacturing of the substance.


Release to the environment of Acetic Acid 80% can occur from industrial use: manufacturing of the substance, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), formulation of mixtures, formulation in materials, in the production of articles, as processing aid, for thermoplastic manufacture, as processing aid and of substances in closed systems with minimal release.


Acetic Acid 80% is used in the following products: coating products, washing & cleaning products, air care products, lubricants and greases, fillers, putties, plasters, modelling clay, anti-freeze products, fertilisers, plant protection products, finger paints, biocides (e.g. disinfectants, pest control products), welding & soldering products and textile treatment products and dyes.


Other release to the environment of Acetic Acid 80% is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).


Industrially, Acetic Acid 80% is used in the preparation of metal acetates, used in some printing processes; vinyl acetate, employed in the production of plastics; cellulose acetate, used in making photographic films and textiles; and volatile organic esters (such as ethyl and butyl acetates), widely used as solvents for resins, paints, and lacquers.


Biologically, Acetic Acid 80% is an important metabolic intermediate, and it occurs naturally in body fluids and in plant juices.
Aside from its uses as a natural preservative and common ingredient in a variety of products, Acetic Acid 80% has also been associated with several impressive health benefits.


In addition to its potent anti-bacterial properties, Acetic Acid 80% is also thought to reduce blood sugar levels, promote weight loss, alleviate inflammation and control blood pressure.
As chemical distributors, the purposes for which this type of Acetic Acid 80% is processed are varied.


As mentioned above, Acetic Acid 80% can be found in many grocery shops as white vinegar.
In such products, Acetic Acid 80% cannot be found in its pure form, but only in small quantities.
Acetic Acid 80% is also present in foods such as canned and pickled foods, cheese and dairy products, sauces or prepared salads.


Acetic Acid 80% is also commonly used in the pharmaceutical, cosmetic and industrial industries both to produce other substances and to regulate their properties, especially with regards to their pH.
Due to its strong odour, one of its other main uses is in cosmetics as a regulator in the aroma of fragrances, i.e. Acetic Acid 80% achieves a balance between sweet smells in particular.


In the textile industry, Acetic Acid 80% is used to dye fabrics and produce fabrics such as viscose or latex.
In the chemical industry, Acetic Acid 80% is used in the production of cleaning products and, in the pharmaceutical industry, in supplements and some medicines, as it is capable of stabilising blood pressure and reducing blood sugar levels.


Acetic Acid 80% is also a common ingredient in ointments.
In households diluted Acetic Acid 80% is often used as a cleaning agent. In the food industry Acetic Acid 80% is used as an acidity regulator.
Acetic Acid 80% is used to make other chemicals, as a food additive, and in petroleum production.


Acetic Acid 80% is used locally, occasionally internally, as a counterirritant and also as a reagent.
Acetic Acid 80% otic (for the ear) is an antibiotic that treats infections caused by bacteria or fungus.
In households, diluted Acetic Acid 80% is often used in descaling agents.


In the food industry, Acetic Acid 80% is controlled by the food additive code E260 as an acidity regulator and as a condiment.
In biochemistry, the acetyl group, derived from Acetic Acid 80%, is fundamental to all forms of life.
When bound to coenzyme A, Acetic Acid 80% is central to the metabolism of carbohydrates and fats.


The global demand for Acetic Acid 80% is about 6.5 million metric tonnes per year (t/a), manufactured from methanol.
Acetic Acid 80%'s production and subsequent industrial use poses health hazards to workers, including incidental skin damage and chronic respiratory injuries from inhalation.


Acetic Acid 80% is a chemical reagent for the production of chemical compounds.
The largest single use of Acetic Acid 80% is in the production of vinyl acetate monomer, closely followed by acetic anhydride and ester production.
The volume of Acetic Acid 80% used in vinegar is comparatively small.


In the field of analytical chemistry, glacial Acetic Acid 80% is widely used in order to estimate substances that are weakly alkaline.
Acetic Acid 80% has a wide range of applications as a polar, protic solvent.
Acetic Acid 80% is used as an antiseptic due to its antibacterial qualities


The manufacture of rayon fiber involves the use of Acetic Acid 80%.
Medically, Acetic Acid 80% has been employed to treat cancer by its direct injection into the tumour.
Being the major constituent of vinegar, Acetic Acid 80% finds use in the pickling of many vegetables.


The manufacture of rubber involves the use of Acetic Acid 80%.
Acetic Acid 80% is also used in the manufacture of various perfumes.
Acetic Acid 80% is widely used in the production of VAM (vinyl acetate monomer).


When two molecules of Acetic Acid 80% undergo a condensation reaction together, the product formed is acetic anhydride.
Acetic Acid 80% is widely used in the industrial preparation of dimethyl terephthalate (DMT).
Acetic Acid 80% is used in the manufacture of acetic anhydride, cellulose acetate, vinyl acetate monomer, acetic esters, chlorAcetic Acid 80%, plastics, dyes, insecticides, photographic chemicals, and rubber.


Other commercial uses of Acetic Acid 80% include the manufacture of vitamins, antibiotics, hormones, and organic chemicals, and as a food additive (acidulant).
Acetic Acid 80% is also used in various textile printing processes.
Acetic Acid 80% is the main component of vinegar, which contains 4 to 18% Acetic Acid 80%.


Acetic Acid 80% is used as a food preservative and food additive (known as E260).
Acetic Acid 80% is used as a raw material and solvent in the production of other chemical products, in oil and gas production, and in the food and pharmaceutical industries.


Large quantities of Acetic Acid 80% are used to make products such as ink for textile printing, dyes, photographic chemicals, pesticides, pharmaceuticals, rubber and plastics.
Acetic Acid 80% is also used in some household cleaning products to remove lime scale.


In foods, Acetic Acid 80% is used for its antibacterial properties, as an acidity stabiliser, diluting colours, as a flavouring agent and for inhibiting mould growth in bread.
Derivatives of Acetic Acid 80% are used as food additives and preservatives, as well as in the production of various chemicals and materials.


In brewing, Acetic Acid 80% is used to reduce excess losses of carbohydrate from the germinated barley and to compensate for production variations, so producing a consistent quality beer.
Acetic Acid 80% can be found in beer, bread, cheese, chutney, horseradish cream, pickles, salad cream, brown sauce, fruit sauce, mint sauce and jelly and tinned baby food, sardines and tomatoes.


Acetic Acid 80% is often used as table vinegar.
Acetic Acid 80% is also used directly as a condiment, and in the pickling of vegetables and other foods.
Acetic Acid 80% is used as the main component in the subsequent synthesis in the process of food and pharmaceutical production.


Food additive Acetic Acid 80% is widely used in marinating, canning, making mayonnaise and sauces and other foods.
In one of Acetic Acid 80%'s most common form, vinegar is also used directly as a condiment, and in the pickling of vegetables and other foods to preserve food against bacteria and fungi.


In brewing, Acetic Acid 80% is used to reduce excess losses of carbohydrate from the germinated barley and to compensate for production variations, so producing a consistent quality beer.
When used as food additive, Acetic Acid 80% has a E number 260.


Acetic Acid 80% can be found in beer, bread, cheese, chutney, horseradish cream, pickles, salad cream, brown sauce, fruit sauce, mint sauce and jelly and tinned baby food, sardines and tomatoes.
Acetic Acid 80% is approved to use as food addictive in EU and generally recognized as safe food substance in the US.


In addition to vinegar, Acetic Acid 80% is used as a food additive and preservative in a variety of other foods, including baked goods, processed meats, cheeses, and condiments.
Many pickled foods, like pickles and sauerkraut, also contain Acetic Acid 80% as a natural byproduct of the fermentation process.


Acetic Acid 80% is also used in the production of various food ingredients, including salts, esters, and anhydrides.
These derivatives of Acetic Acid 80% are used as preservatives, flavorings, and emulsifiers in processed foods.
Some examples of these derivatives include sodium acetate, ethyl acetate, and acetic anhydride.


Acetic Acid 80% is also used in the production of various adhesives, coatings, and inks, and is used to produce cellulose acetate, which is used in photographic films and other applications.
Acetic Acid 80% is found naturally in many foods and is also produced synthetically for a variety of industrial applications.


Acetic Acid 80% is one of the simplest carboxylic acid.
It has a variety of uses, ranging from food and medical to industrial.
As mentioned earlier, Acetic Acid 80% is primarily found in vinegar.


Acetic Acid 80%'s also used as food additive (E number E260) for regulating acidity and as a preservative.
Acetic Acid 80% is also essential in the pickling process, which involves preserving vegetables or fruits (such as cucumbers, beets, or watermelon rind) in vinegar.


Acetic Acid 80% helps to prevent the growth of harmful bacteria and preserves the vegetables or fruits' natural color, flavor, and texture.
Pickling is a common technique used to preserve foods, especially in countries with long winter seasons where fresh produce is not available.
Acetic Acid 80% can also be used to produce synthetic fabrics that resemble natural ones such as silk, wool or cotton.


Acetic Acid 80% is used in the production of a wide range of chemicals and materials, such as vinyl acetate monomer (VAM), cellulose acetate, and acetic anhydride.
These chemicals are used in various industries, including textiles, plastics, coatings, and adhesives.


Acetic Acid 80% can be used to increase the acidity (and lower the pH) of food products as well as improve the organoleptic quality by giving the product an acid flavor, such as salt and vinegar chips.
Acetic Acid 80% is also a popular preservative as it stops bacterial growth in dressings, sauces, cheese, and pickles.


Acetic Acid 80%/vinegar is used to pickle foods, which is a type of preservation method. When used with baking soda, Acetic Acid 80% also works as a chemical leavening agent.
Besides food, Acetic Acid 80% has been used in medicine, such as in ear drops, and a number of industrial processes.


Acetic Acid 80% is used to make cellulose acetate and polyvinyl acetate and glacial Acetic Acid 80% in particular is frequently used as a solvent.
As mentioned before, Acetic Acid 80% is extensively used as a food preservative.
Acetic Acid 80% makes foods less hospitable to harmful bacteria that can cause food poisoning.


When used in small amounts, Acetic Acid 80% can effectively extend the shelf life of food items.
Furthermore, Acetic Acid 80% can also be added to pickling liquid to help maintain the pickled product's acidity level, thereby making it last longer.
Another popular application of Acetic Acid 80% is as a natural food flavour enhancer.


Along with improving the taste of many processed foods including sauces, dressings, and condiments, Acetic Acid 80% is also used to provide a sour tang to beverages like soda and energy drinks.
Acetic Acid 80% is added in small amounts to these products in order to impart a tart, refreshing taste that many consumers prefer.


Acetic Acid 80% is used in a wide variety of household cleaning products, including all-purpose cleaners, glass cleaners, and bathroom cleaning solutions.
In addition to its use in household cleaners, Acetic Acid 80% is also used as a natural weed killer.
Acetic Acid 80% can be sprayed on weeds in gardens and lawns to kill them without contaminating the soil.


Some environmentally conscious gardeners prefer using vinegar sprays instead of toxic chemical herbicides, as Acetic Acid 80% is considered a more eco-friendly solution.
Some research has also shown that Acetic Acid 80% may have potential health benefits.


For instance, Acetic Acid 80% has been studied for its potential to lower blood sugar levels and improve insulin sensitivity.
In addition, Acetic Acid 80% may help with weight loss by reducing appetite and promoting feelings of fullness.
However, more research is needed to fully understand the potential health benefits of Acetic Acid 80%.


In terms of safety, Acetic Acid 80% should be handled with care.
To summarize, Acetic Acid 80% is a versatile ingredient with numerous applications.
Acetic Acid 80% is commonly used as a food preservative, flavour enhancer, and cleaning agent.


Acetic Acid 80% also has potential health benefits, although further research is needed to confirm these benefits.
As with any chemical, Acetic Acid 80% should be handled with care and stored properly to minimize risk of injury or damage to property.
In conclusion, Acetic Acid 80% is a widely-used food ingredient with many applications and benefits.


Acetic Acid 80% is a natural substance that is safe when used appropriately.
Whether you're using it in the kitchen or for cleaning purposes, Acetic Acid 80% is a versatile and effective solution that has been relied upon for centuries.
Acetic Acid 80% is a versatile and widely-used food ingredient with a range of possible benefits and applications, as well as a few drawbacks.


Understanding the properties and uses of Acetic Acid 80% is essential for anyone working with food or chemicals.
In addition to Acetic Acid 80%, there are other types of acids that are used in food production, such as ascorbic acid (vitamin C), citric acid, and malic acid.
These acids are commonly used as preservatives, stabilizers, flavor enhancers, and acidulants, depending on the specific product formulation.


While each type of acid has its own unique properties, Acetic Acid 80% stands out for its sour taste and pungent aroma.
One of the key applications of Acetic Acid 80% is in the production of vinegar, which is a widely-used condiment that is made by fermenting ethanol and other sugars.


Apple cider vinegar, balsamic vinegar, and white vinegar are some of the most popular vinegar varieties available.
Each type of vinegar has Acetic Acid 80%'s own unique flavor and can be used in a range of recipes, from marinades to salad dressings.
Acidity regulator Acetic Acid 80% is commonly used in food as a preservative and flavoring agent.


Acetic Acid 80% is primarily used to regulate the acidity levels in various food products, including pickles, sauces, dressings, and condiments.
Additionally, acidity regulator Acetic Acid 80% is effective in preventing the growth of bacteria and fungi in food, extending its shelf life.
Acetic Acid 80% is considered safe for consumption when used within the approved limits set by regulatory authorities.


Acetic Acid 80% is commonly used in pickled vegetables, dressings, sauces, and condiments to provide tartness and enhance flavors.
Acetic Acid 80% has been used in food preservation and flavoring for centuries.
Acetic Acid 80% is a commonly used additive in the food industry.


Acetic Acid 80% is a natural acid found in vinegar and is widely used as a food preservative and flavoring agent.
Acetic Acid 80% is known for its sour taste and is often added to various food products such as pickles, sauces, condiments, and dressings to enhance their flavor and extend their shelf life.


As a food preservative, Acetic Acid 80% works by creating an acidic environment that inhibits the growth of bacteria and other microorganisms.
This helps to prevent food spoilage and increase Acetic Acid 80%'s stability.
Acetic Acid 80% also acts as a pH regulator, helping to maintain the desired acidity level in certain foods.


As with any food additive, it is recommended to consume foods containing Acetic Acid 80% in moderation and as part of a balanced diet.
In conclusion, Acetic Acid 80% is a widely used food additive that serves both as a preservative and a flavor enhancer.
Acetic Acid 80% provides a sour taste and helps to extend the shelf life of various food products.


-Acetic Acid 80% with formula CH3COOH or food additive E260 is used:
*food industry – known as additive E260, is involved in the production of dairy products, salads, sauces, dressings, marinades and canned food;
*Pharmaceutical industry – is part of aspirin, phenacetin, other drugs and dietary supplements that stabilize blood pressure and reduce blood sugar;
*textile industry – as a component for the manufacture and dyeing of rayon, latex fabrics;
*cosmetic sphere – used to balance the smell and regulate the characteristics of various compositions;
*chemical industry – production of cleaning and detergents, household chemicals, acetone, synthetic dyes;
*as a solvent for varnishes, latex coagulant;
*as an acetylating agent in organic synthesis;
*salts of Acetic Acid 80% (Fe, Al, Cr, etc.) – mordants for dyeing, etc.


-Breeding of bees:
Acetic Acid 80% fumigation will kill a wide variety of pathogens, such as the causative agents of Cretaceous brood, European foulbrood, Nosema and Amoeba.
Acetic Acid 80% will also eliminate all stages of the wax moth except the pupae.


-Vinyl acetate monomer:
Production of vinyl acetate monomer (VAM), the application consumes approximately 40% to 45% of the world's Acetic Acid 80% production.
The reaction is with ethylene and Acetic Acid 80% with oxygen over a palladium catalyst.


-Ester production:
Acetic Acid 80% esters are used as a solvent in inks, paints and coatings.
Esters include ethyl acetate, n-butyl acetate, isobutyl acetate, and propyl acetate


-Use as a solvent:
Acetic Acid 80% is an excellent polar protic solvent.
Acetic Acid 80% is often used as a recrystallization solvent to purify organic compounds.
Acetic Acid 80% is used as a solvent in the production of terephthalic acid (TPA), a raw material for the production of polyethylene terephthalate (PET).


-Medical use of Acetic Acid 80%:
Acetic Acid 80% injection into a tumor has been used to treat cancer since the 1800s.
Acetic Acid 80% is used as part of cervical cancer screening in many areas in the developing world.

The acid is applied to the cervix and if an area of white appears after about a minute the test is positive.
Acetic Acid 80% is an effective antiseptic when used as a 1% solution, with broad spectrum of activity against streptococci, staphylococci, pseudomonas, enterococci and others.

Acetic Acid 80% may be used to treat skin infections caused by pseudomonas strains resistant to typical antibiotics.
While diluted Acetic Acid 80% is used in iontophoresis, no high quality evidence supports this treatment for rotator cuff disease.
As a treatment for otitis externa, it is on the World Health Organization's List of Essential Medicines.


-Foods uses of Acetic Acid 80%:
Acetic Acid 80% has 349 kcal (1,460 kJ) per 100 g.
Vinegar is typically no less than 4% Acetic Acid 80% by mass.
Legal limits on Acetic Acid 80% content vary by jurisdiction.

Vinegar is used directly as a condiment, and in the pickling of vegetables and other foods.
Table vinegar tends to be more diluted (4% to 8% Acetic Acid 80%), while commercial food pickling employs solutions that are more concentrated.
The proportion of Acetic Acid 80% used worldwide as vinegar is not as large as industrial uses, but it is by far the oldest and best-known application.


-Acetic Acid 80% as a Solvent:
In its liquid state, CH3COOH is a hydrophile (readily dissolves in water) and also a polar, protic solvent.
A mixture of Acetic Acid 80% and water is, in this manner, similar to a mixture of ethanol and water.
Acetic Acid 80% also forms miscible mixtures with hexane, chloroform, and several oils.
However, Acetic Acid 80% does not form miscible mixtures with long-chain alkanes (such as octane).


-Vinyl acetate monomer:
The primary use of Acetic Acid 80% is the production of vinyl acetate monomer (VAM).
In 2008, this application was estimated to consume a third of the world's production of Acetic Acid 80%.

The reaction consists of ethylene and Acetic Acid 80% with oxygen over a palladium catalyst, conducted in the gas phase.
2 H3C−COOH + 2 C2H4 + O2 → 2 H3C−CO−O−CH=CH2 + 2 H2O
Vinyl acetate can be polymerised to polyvinyl acetate or other polymers, which are components in paints and adhesives


-Ester production:
The major esters of Acetic Acid 80% are commonly used as solvents for inks, paints and coatings.
The esters include ethyl acetate, n-butyl acetate, isobutyl acetate, and propyl acetate.

They are typically produced by catalyzed reaction from Acetic Acid 80% and the corresponding alcohol:
CH3COO−H + HO−R → CH3COO−R + H2O, R = general alkyl group
For example, Acetic Acid 80% and ethanol gives ethyl acetate and water.
CH3COO−H + HO−CH2CH3 → CH3COO−CH2CH3 + H2O

Most acetate esters, however, are produced from acetaldehyde using the Tishchenko reaction.
In addition, ether acetates are used as solvents for nitrocellulose, acrylic lacquers, varnish removers, and wood stains.
First, glycol monoethers are produced from ethylene oxide or propylene oxide with alcohol, which are then esterified with Acetic Acid 80%.

The three major products are ethylene glycol monoethyl ether acetate (EEA), ethylene glycol monobutyl ether acetate (EBA), and propylene glycol monomethyl ether acetate (PMA, more commonly known as PGMEA in semiconductor manufacturing processes, where it is used as a resist solvent).
This application consumes about 15% to 20% of worldwide Acetic Acid 80%.
Ether acetates, for example EEA, have been shown to be harmful to human reproduction.


-Acetic anhydride:
The product of the condensation of two molecules of Acetic Acid 80% is acetic anhydride.
The worldwide production of acetic anhydride is a major application, and uses approximately 25% to 30% of the global production of Acetic Acid 80%.
The main process involves dehydration of Acetic Acid 80% to give ketene at 700–750 °C.

Ketene is thereafter reacted with Acetic Acid 80% to obtain the anhydride:
CH3CO2H → CH2=C=O + H2O
CH3CO2H + CH2=C=O → (CH3CO)2O

Acetic anhydride is an acetylation agent.
As such, Acetic Acid 80%'s major application is for cellulose acetate, a synthetic textile also used for photographic film.
Acetic anhydride is also a reagent for the production of heroin and other compounds.


-Use as solvent:
As a polar protic solvent, Acetic Acid 80% is frequently used for recrystallization to purify organic compounds.
Acetic Acid 80% is used as a solvent in the production of terephthalic acid (TPA), the raw material for polyethylene terephthalate (PET).
In 2006, about 20% of Acetic Acid 80% was used for TPA production.

Acetic Acid 80% is often used as a solvent for reactions involving carbocations, such as Friedel-Crafts alkylation.
For example, one stage in the commercial manufacture of synthetic camphor involves a Wagner-Meerwein rearrangement of camphene to isobornyl acetate; here Acetic Acid 80% acts both as a solvent and as a nucleophile to trap the rearranged carbocation.


-Vinegar:
The vinegar is usually 4-18 wt.% Acetic Acid 80%.
Acetic Acid 80% is used directly as a seasoning and marinade of vegetables and other food products.
Table vinegar is used more often more diluted (4% to 8% Acetic Acid 80%), while a more concentrated solution is used for pickling in commercial foods.


-Industrial Use:
Acetic Acid 80% is used in many industrial processes for the production of substrates and it is often used as a chemical reagent for the production of a number of chemical compounds like acetic anhydride, ester, vinyl acetate monomer, vinegar, and many other polymeric materials.
Acetic Acid 80% is also used to purify organic compounds as it can be used as a solvent for recrystallization.


-Industrial applications of Acetic Acid 80%:
As one of the important organic acids, Acetic Acid 80% is mainly used in the synthesis of vinyl acetate, cellulose acetate, acetic anhydride, acetate, metal acetate and halogenated Acetic Acid 80%.

Glacial Acetic Acid 80% is also an important raw material for pharmaceuticals, dyes, pesticides and other organic synthesis.
In addition, Acetic Acid 80% is also widely used in the manufacture of photographic medicines, cellulose acetate, fabric printing and dyeing, and the rubber industry.


-Food applications of Acetic Acid 80%:
In the food industry, Acetic Acid 80% is generally used as an acidulant, flavor enhancer and spice manufacturing.

*Synthetic vinegar:
Dilute Acetic Acid 80% to 4-5% with water, add various flavoring agents, the flavor is similar to alcohol vinegar, the production time is short, and the price is cheap.

As a sour agent, glacial Acetic Acid 80% can be used in compound seasonings, prepared vinegar, canned food, jelly and cheese, and used in moderation according to production needs.
Acetic Acid 80% can also be used as a flavor enhancer, and the recommended dosage is 0.1-0.3 g/kg.


-Medical Use:
Acetic Acid 80% has a lot of uses in the medical field.
The most important uses here are that Acetic Acid 80% can be used as an antiseptic against pseudomonas, enterococci, streptococci, staphylococci, and others.
Acetic Acid 80% is also used in cervical cancer screening and for the treatment of infections.
Further, Acetic Acid 80% is used as an agent to lyse red blood cells before white blood cells are examined.
Vinegar has also been said to reduce high concentrations of blood sugar.


-Important and Popular Uses of Acetic Acid 80%:
There are many uses of Acetic Acid 80%.
So, in addition to being treated just as a food preservative (vinegar), the acid is used in many areas and instances.

Some top and important uses include:
*Industrial Use
*Medicinal Uses
*Household
*Food Industry


-Food Industry:
In the food industry, Acetic Acid 80% finds its use most commonly in commercial pickling operations, and in condiments like mayonnaise, mustard, and ketchup.
Acetic Acid 80% is also used for seasoning various food items like salads etc.
Additionally, vinegar can react with alkaline ingredients like baking soda and when that happens it produces a gas that helps to make baked goods become.


-Household Uses:
Acetic Acid 80% which is a dilute solution is used extensively as vinegar.
And as we are familiar, vinegar is widely used for cleaning, laundry, cooking, and many other household uses.

Farmers usually spray Acetic Acid 80% on livestock silage to counter bacterial and fungal growth.
Apart from these, Acetic Acid 80% is used for the manufacture of inks and dyes and it is also used in making perfumes.
Acetic Acid 80% is also involved in the manufacturing of rubber and plastic industries.



USES AND BENEFITS OF ACETIC ACID 80%
One of the most common ways consumers may come into contact with Acetic Acid 80% is in the form of household vinegar, which is naturally made from fermentable sources such as wine, potatoes, apples, grapes, berries and grains.

Vinegar is a clear solution generally containing about 5 percent Acetic Acid 80% and 95 percent water.
Vinegar is used as a food ingredient and can also be an ingredient in personal care products, household cleaners, pet shampoos and many other products for the home:

-vinegar and baking soda
*Food Preparation:
Vinegar is a common food ingredient, often used as a brine in pickling liquids, vinaigrettes, marinades and other salad dressings.
Vinegar also can be used in food preparation to help control Salmonella contamination in meat and poultry products.

*Cleaning:
Vinegar can be used throughout the home as a window cleaner, to clean automatic coffee makers and dishes, as a rinsing agent for dishwashers, and to clean bathroom tile and grout.
Vinegar can also be used to clean food-related tools and equipment because it generally does not leave behind a harmful residue and requires less rinsing.

*Gardening:
In concentrations of 10 to 20 percent, Acetic Acid 80% can be used as a weed killer on gardens and lawns.
When used as an herbicide, the Acetic Acid 80% can kill weeds that have emerged from the soil, but does not affect the roots of the weed, so they can regrow.

When Acetic Acid 80% is at 99.5 percent concentration, it is referred to as glacial Acetic Acid 80%.
Glacial Acetic Acid 80% has a variety of uses, including as a raw material and solvent in the production of other chemical products.



INDUSTRIAL APPLICATIONS FOR ACETIC ACID 80% INCLUDE:
*Vinyl Acetate, cellulose fibers and plastics:
Acetic Acid 80% is used to make many chemicals, including vinyl acetate, acetic anhydride and acetate esters.
Vinyl acetate is used to make polyvinyl acetate, a polymer used in paints, adhesives, plastics and textile finishes.

Acetic anhydride is used in the manufacture of cellulose acetate fibers and plastics used for photographic film, clothing and coatings.
Acetic Acid 80% is also used in the chemical reaction to produce purified terephthalic acid (PTA), which is used to manufacture the PET plastic resin used in synthetic fibers, food containers, beverage bottles and plastic films.

*Solvents:
Acetic Acid 80% is a hydrophilic solvent, similar to ethanol.
Acetic Acid 80% dissolves compounds such as oils, sulfur and iodine and mixes with water, chloroform and hexane.

*Acidizing oil and gas:
Acetic Acid 80% can help reduce metal corrosion and scale build-up in oil and gas well applications.
Acetic Acid 80% is also used in oil well stimulation to improve flow and increase production of oil and gas.

*Pharmaceuticals and vitamins:
The pharmaceutical industry uses Acetic Acid 80% in the manufacture of vitamins, antibiotics, hormones and other products.

*Food Processing:
Acetic Acid 80% is commonly used as a cleaning and disinfecting product in food processing plants.

*Other uses:
Salts of Acetic Acid 80% and various rubber and photographic chemicals are made from Acetic Acid 80%.
Acetic Acid 80% and its sodium salt are commonly used as a food preservative.



WHAT CAN YOU USE ACETIC ACID 80% FOR?
*Removing stubborn limescale on sanitary facilities and kitchen appliances.
*Combating green deposits on terraces, garden furniture and stone surfaces.
*Descaling of industrial machines and equipment.
*Cleaning and disinfection in the food industry, if adequately diluted.
*Use as raw material in chemical synthesis for the production of esters, acetic esters and various organic compounds.
*In agriculture for regulating the pH value of the soil.
*As a preservative in food processing, for example when pickling vegetables.
*Cleaning and restoration of facades and monuments.



USES OF ACETIC ACID 80%:
The chemical reagent for the processing of chemical compounds is Acetic Acid 80%.
In the production of vinyl acetate monomer, acetic anhydride, and ester production, the use of Acetic Acid 80% is important.


*Vinyl Acetate Monomer:
Vinyl acetate monomer (VAM) processing is the main application of Acetic Acid 80%.
Vinyl acetate undergoes polymerization to produce polyvinyl acetate or other polymers, which are components of paints and adhesives.

The reaction consists of ethylene and Acetic Acid 80% with oxygen over a palladium catalyst.
2CH3COOH+2C2H4+O2→2CH3CO2CH=CH2+2H2O
Wood glue also utilizes vinyl acetate polymers.

*Acetic Anhydride:
Acetic anhydride is the result of the condensation of two Acetic Acid 80% molecules.
Significant use is the worldwide processing of acetic anhydride, utilizing about 25 per cent to 30 per cent of global Acetic Acid 80% production.
The key method includes Acetic Acid 80% dehydration to give ketene at 700-750 °C.

CH3CO2H→CH2=C=O+H2O
CH3CO2H+CH2=C=O→CH3CO2O

It is great for general disinfection and fighting mould and mildew since Acetic Acid 80% kills fungi and bacteria.
Acetic Acid 80% is useful in a range of traditional and green cleaning materials, such as mould and mildew cleaners, floor cleaners, sprays for cleaning and dusting, and roof cleaners, either as vinegar or as an element.

The acetyl group is in use widely in the biochemistry field.
Products made from Acetic Acid 80% are an effective metabolizer of carbohydrates and fats when bound to coenzyme A.
As a treatment for otitis externa, Acetic Acid 80% is the best and most effective drug in a health system on the World Health Organization’s List of Essential Medicines.



INDUSTRIAL APPLICATION OF ACETIC ACID 80%:
Thanks to its versatile properties, Acetic Acid 80% plays a vital role in various European industries.

*In the chemical industry, Acetic Acid 80% is a fundamental building block for producing numerous chemicals.
One example is vinyl acetate monomer (VAM), which Acetic Acid 80% is widely used to manufacture adhesives, paints, and coatings.
Acetic Acid 80% is also an essential precursor for producing acetic anhydride, esters, and cellulose acetate.

*The food and beverage industry extensively utilizes Acetic Acid 80% as a preservative and flavoring agent.
Vinegar, primarily composed of Acetic Acid 80%, finds widespread use in cooking, pickling, and salad dressings.

*In the pharmaceutical industry, Acetic Acid 80% is a crucial intermediate in synthesizing pharmaceuticals, including antibiotics, vitamins, and analgesics.
Acetic Acid 80%'s versatile nature allows for the production of a wide range of medications.

*The textile industry relies on Acetic Acid 80% to manufacture synthetic acetate fibers.
Acetate fibers are commonly used in clothing, upholstery, and textiles due to their excellent draping properties and durability.



WHAT IS ACETIC ACID 80% IN FOOD?
Acetic Acid 80% is a food additive that is commonly used as a preservative, flavor enhancer, and pH regulator.
Acetic Acid 80% is a natural acid found in vinegar and is also produced synthetically for use in food applications.
Acetic Acid 80% is generally regarded as safe for consumption at low levels, and it is commonly used in condiments, pickled foods, sauces, and dressings to provide a tangy taste and extend shelf life.
However, excessive consumption of Acetic Acid 80% can cause irritation to the digestive system.
As with any food additive, it is important to consume Acetic Acid 80% in moderation and maintain a balanced diet.



ACETIC ACID 80% IN EVERYDAY LIFE:
Acetic Acid 80% is found in many everyday products as described above, such as food, cleaning products and cosmetics, among others.
Of all of them, vinegar is one of the most important ones, as Acetic Acid 80% has different uses, such as for cooking or cleaning.
Acetic Acid 80% is an infallible product when it comes to dealing with stubborn stains such as dog urine, rust or other dirt.



PHYSICAL PROPERTIES OF ACETIC ACID 80%:
Acetic Acid 80% is a colorless liquid; with a strong vinegar-like odour.
Acetic Acid 80% is considered a volatile organic compound by the National Pollutant Inventory.
Specific Gravity: 1.049 @ 25°C
Melting Point: 16.7°C
Boiling Point: 118°C
Vapour pressure: 1.5 kPa @ 20°C



CHEMICAL PROPERTIES OF ACETIC ACID 80%:
Acetic Acid 80% is hygroscopic, meaning that it tends to absorb moisture.
Acetic Acid 80% mixes with ethyl alcohol, glycerol, ether, carbon tetrachloride and water and reacts with oxidants and bases.
Concentrated Acetic Acid 80% is corrosive and attacks many metals forming flammable or explosive gases.
Acetic Acid 80% can also attack some forms of plastic, rubber and coatings.



HEALTH BENEFITS OF ACETIC ACID 80%:
1. Kills Bacteria:
Vinegar has long been used as a natural disinfectant, largely due to its content of Acetic Acid 80%.
Acetic Acid 80% has powerful antibacterial properties and can be effective at killing off several specific strains of bacteria.

In fact, one 2014 in vitro study found that Acetic Acid 80% was able to block the growth of myobacteria, a genus of bacteria responsible for causing tuberculosis and leprosy.
Other research shows that vinegar may also protect against bacterial growth, which may be partially due to the presence of Acetic Acid 80%.


2. Reduces Blood Pressure:
Not only does high blood pressure place extra strain on the heart muscle and cause it to slowly weaken over time, but high blood pressure is also a major risk factor for heart disease.
In addition to modifying your diet and exercise routine, promising research has found that Acetic Acid 80% may also help control blood pressure.


3. Decreases Inflammation:
Acute inflammation plays an important role in immune function, helping to defend the body against illness and infection.
Sustaining high levels of inflammation long-term, however, can have a detrimental effect on health, with studies showing that inflammation could contribute to the development of chronic conditions like heart disease and cancer.
Acetic Acid 80% is thought to reduce inflammation to help protect against disease.


4. Supports Weight Loss:
Some research suggests that Acetic Acid 80% could help support weight control by aiding in weight loss.


5. Promotes Blood Sugar Control:
Apple cider vinegar has been well-studied for its ability to support blood sugar control.
Research shows that Acetic Acid 80%, one of the primary components found in apple cider vinegar, may play a role in its powerful blood sugar-lowering properties.

In one study, consuming vinegar with Acetic Acid 80% alongside a high-carb meal was found to reduce blood sugar and insulin levels thanks to its ability to slow down the emptying of the stomach.
Another in vitro study had similar findings, reporting that Acetic Acid 80% decreased the activity of several enzymes involved in carbohydrate metabolism, which could decrease the absorption of carbs and sugar in the small intestine.



NOMENCLATURE OF ACETIC ACID 80%:
The trivial name "Acetic Acid 80%" is the most commonly used and preferred IUPAC name.
The systematic name "ethanoic acid", a valid IUPAC name, is constructed according to the substitutive nomenclature.
The name "Acetic Acid 80%" derives from the Latin word for vinegar, "acetum", which is related to the word "acid" itself.

"Glacial Acetic Acid 80%" is a name for water-free (anhydrous) Acetic Acid 80%.
Similar to the German name "Eisessig" ("ice vinegar"), the name comes from the solid ice-like crystals that form with agitation, slightly below room temperature at 16.6 °C (61.9 °F).

Acetic Acid 80% can never be truly water-free in an atmosphere that contains water, so the presence of 0.1% water in glacial Acetic Acid 80% lowers its melting point by 0.2 °C.
A common symbol for Acetic Acid 80% is AcOH (or HOAc), where Ac is the pseudoelement symbol representing the acetyl group CH3−C(=O)−; the conjugate base, acetate (CH3COO−), is thus represented as AcO−.

(The symbol Ac for the acetyl functional group is not to be confused with the symbol Ac for the element actinium; context prevents confusion among organic chemists).
To better reflect its structure, Acetic Acid 80% is often written as CH3−C(O)OH, CH3−C(=O)OH, CH3COOH, and CH3CO2H.

In the context of acid–base reactions, the abbreviation HAc is sometimes used, where Ac in this case is a symbol for acetate (rather than acetyl).
Acetate is the ion resulting from loss of H+ from Acetic Acid 80%.
The name "acetate" can also refer to a salt containing this anion, or an ester of Acetic Acid 80%.



HISTORY OF ACETIC ACID 80%:
Vinegar was known early in civilization as the natural result of exposure of beer and wine to air because Acetic Acid 80%-producing bacteria are present globally.
The use of Acetic Acid 80% in alchemy extends into the third century BC, when the Greek philosopher Theophrastus described how vinegar acted on metals to produce pigments useful in art, including white lead (lead carbonate) and verdigris, a green mixture of copper salts including copper(II) acetate.

Ancient Romans boiled soured wine to produce a highly sweet syrup called sapa.
Sapa that was produced in lead pots was rich in lead acetate, a sweet substance also called sugar of lead or sugar of Saturn, which contributed to lead poisoning among the Roman aristocracy.

In the 16th-century German alchemist Andreas Libavius described the production of acetone from the dry distillation of lead acetate, ketonic decarboxylation.

The presence of water in vinegar has such a profound effect on Acetic Acid 80%'s properties that for centuries chemists believed that glacial Acetic Acid 80% and the acid found in vinegar were two different substances.
French chemist Pierre Adet proved them identical.


*Crystallised Acetic Acid 80%
In 1845 German chemist Hermann Kolbe synthesised Acetic Acid 80% from inorganic compounds for the first time.
This reaction sequence consisted of chlorination of carbon disulfide to carbon tetrachloride, followed by pyrolysis to tetrachloroethylene and aqueous chlorination to trichloroAcetic Acid 80%, and concluded with electrolytic reduction to Acetic Acid 80%.

By 1910, most glacial Acetic Acid 80% was obtained from the pyroligneous liquor, a product of the distillation of wood.
The Acetic Acid 80% was isolated by treatment with milk of lime, and the resulting calcium acetate was then acidified with sulfuric acid to recover Acetic Acid 80%.
At that time, Germany was producing 10,000 tons of glacial Acetic Acid 80%, around 30% of which was used for the manufacture of indigo dye.

Because both methanol and carbon monoxide are commodity raw materials, methanol carbonylation long appeared to be attractive precursors to Acetic Acid 80%.
Henri Dreyfus at British Celanese developed a methanol carbonylation pilot plant as early as 1925.

However, a lack of practical materials that could contain the corrosive reaction mixture at the high pressures needed (200 atm or more) discouraged commercialization of these routes.
The first commercial methanol carbonylation process, which used a cobalt catalyst, was developed by German chemical company BASF in 1963.

In 1968, a rhodium-based catalyst (cis−[Rh(CO)2I2]−) was discovered that could operate efficiently at lower pressure with almost no by-products.
US chemical company Monsanto Company built the first plant using this catalyst in 1970, and rhodium-catalyzed methanol carbonylation became the dominant method of Acetic Acid 80% production (see Monsanto process).

In the late 1990s, BP Chemicals commercialised the Cativa catalyst ([Ir(CO)2I2]−), which is promoted by iridium for greater efficiency.
Known as the Cativa process, the iridium-catalyzed production of glacial Acetic Acid 80% is greener, and has largely supplanted the Monsanto process, often in the same production plants.


*Interstellar medium
Interstellar Acetic Acid 80% was discovered in 1996 by a team led by David Mehringer using the former Berkeley-Illinois-Maryland Association array at the Hat Creek Radio Observatory and the former Millimeter Array located at the Owens Valley Radio Observatory.

It was first detected in the Sagittarius B2 North molecular cloud (also known as the Sgr B2 Large Molecule Heimat source).
Acetic Acid 80% has the distinction of being the first molecule discovered in the interstellar medium using solely radio interferometers; in all previous ISM molecular discoveries made in the millimetre and centimetre wavelength regimes, single dish radio telescopes were at least partly responsible for the detections.



PHYSICAL DETAILS AND PROPERTIES OF ACETIC ACID 80%:
Acetic Acid 80%, or ethanoic acid, is a clear, colorless liquid with a pungent vinegar-like odor.
Acetic Acid 80% has a molecular formula CH₃COOH and a molecular weight of 60.05 g/mol.
With a boiling point of 118.1, °C and a melting point of 16.6°C, Acetic Acid 80% is highly soluble in water and miscible with most organic solvents.
These physical properties make Acetic Acid 80% a versatile compound for various industrial applications.



PRODUCTION METHODS OF ACETIC ACID 80%:
Acetic Acid 80% is primarily produced through two main methods: methanol carbonylation and oxidation of acetaldehyde.
The first method, methanol carbonylation, is the most common process for large-scale Acetic Acid 80% production.
Acetic Acid 80% involves the reaction of methanol with carbon monoxide in the presence of a catalyst, typically rhodium or iodine compounds.

This catalytic reaction yields Acetic Acid 80% as the primary product.
The second method involves the oxidation of acetaldehyde. Acetaldehyde can be oxidized using various catalysts, including palladium or copper, producing Acetic Acid 80% as a byproduct.



WHAT IS THE PURPOSE OF ACETIC ACID 80% IN ADDITIVES FOODS?
Acetic Acid 80% is commonly used as a food additive.
Acetic Acid 80% serves multiple purposes in additives foods.
Firstly, Acetic Acid 80% acts as a preservative by inhibiting the growth of bacteria and fungi, thus extending the shelf life of the product.
Secondly, Acetic Acid 80% enhances the flavor and aroma of the food by giving it a tangy and sour taste.
Additionally, Acetic Acid 80% can also be used as an acidity regulator and pH control agent in certain food products.



FUNCTIONS OF ACETIC ACID 80%:
1. Acidity Regulator / Buffering Agent - Changes or maintains the acidity or basicity of food/cosmetics.
2. Drug / Medicine - Treats, alleviates, cures, or prevents sickness. As officially declared by a governmental drug/medicine regulatory body
3. Exfoliant - Removes dead cells at the surface of the skin
4. Experimental / Patented - Relatively new ingredient with limited data available
5. Insecticide / Pesticide - Kills or inhibits unwanted organisms
6. Preservative - Prevents and inhibits the growth of unwanted microorganisms which may be harmful
7. Solvent (Cosmetics) - Enhances the properties of other ingredients



IS ACETIC ACID 80% SAFE?
Acetic Acid 80% is also known as Acetic Acid 80%, which is a widely used food additive.
Acetic Acid 80% is considered safe for consumption by regulatory authorities such as the Food and Drug Administration (FDA) and the European Food Safety Authority (EFSA).



HEALTH BENEFITS OF ACETIC ACID 80%:
Acetic Acid 80% has powerful antibacterial properties.
Acetic Acid 80% helps to reduce blood pressure.
Acetic Acid 80% also help to reduce inflammation.
Acetic Acid 80% promotes blood sugar control.
Acetic Acid 80% also supports weight loss.



FUNCTION & CHARACTERISTICS OF ACETIC ACID 80%:
Acetic Acid 80% is used as a preservative against bacteria and fungi.
In mayonnaise Acetic Acid 80% is added to increase the inactivation of Salmonella .
The highest activity of Acetic Acid 80% is at low pH.
Acetic Acid 80% can also be used as a buffer in acidic foods.
Acetic Acid 80% is also used as an aroma component.



ORIGIN OF ACETIC ACID 80%:
Natural acid, present in most fruits.
Acetic Acid 80% is produced by bacterial fermentation and thus present in all fermented products.
Commercially produced by bacterial fermentation of sugar, molasses or alcohol or by chemical synthesis from acetealdehyde.



IS ACETIC ACID 80% GLUTEN FREE?
Yes.
Acetic Acid 80% is gluten free and widely used in gluten free food to provide sour taste to sour drinks.



WHY IS ACETIC ACID 80% GLUTEN FREE?
Gluten is a type of elastic grain protein that helps wheat, rye and barley hold their shape.
Because of its glue-like properties, gluten is often added to other food products—pasta, sauces, crackers, baked goods—to thicken or bind those products together.
Raw materials used in manufacturing of Acetic Acid 80% are Acetyl ketene; So the manufacturing process of it is gluten free.
So, Acetic Acid 80% is gluten free.



IS ACETIC ACID 80% SAFE FOR CONSUMPTION IN ADDITIVES FOODS?
Acetic Acid 80% is considered safe for consumption in additives foods.
Acetic Acid 80% is a naturally occurring substance and is commonly found in vinegar.
Acetic Acid 80% is used as a flavoring agent and food preservative in various processed foods.
However, Acetic Acid 80% is important to note that excessive consumption of Acetic Acid 80% may have adverse effects on health.
Acetic Acid 80% is always recommended to consume additives foods in moderation and as part of a balanced diet.



HOW DOES ACETIC ACID 80% CONTRIBUTE TO THE PRESERVATION OF ADDITIVES FOODS?
Acetic Acid 80% contributes to the preservation of additives foods in several ways.
Firstly, Acetic Acid 80% has antimicrobial properties that inhibit the growth of bacteria, yeasts, and molds, reducing the risk of food spoilage and extending the shelf life of products.

Additionally, Acetic Acid 80% acts as a pH regulator in additives foods.
Acetic Acid 80% helps maintain acidity levels, creating an environment that is unfavorable for the growth of certain microorganisms.
This is particularly important in canned and pickled foods where acidity plays a crucial role in preventing the growth of harmful bacteria like Clostridium botulinum.

Moreover, Acetic Acid 80% also contributes to the preservation of additives foods by enhancing flavor.
Acetic Acid 80% adds a characteristic tartness or sourness, which can improve the taste profile of various products.
By enhancing the overall sensory experience, Acetic Acid 80% can help prolong the consumer acceptability and consumption of additives foods.

In summary, Acetic Acid 80% plays a vital role in preserving additives foods by acting as an antimicrobial agent, pH regulator, and flavor enhancer.
Acetic Acid 80%'s usage ensures the safety and prolonged shelf life of various food products.
In conclusion, Acetic Acid 80% plays a crucial role as an additive in the food industry.

With its versatile properties, Acetic Acid 80% enhances flavors and acts as a natural preservative, increasing the shelf life of various food products.
Despite some concerns about its safety and potential health effects, research suggests that when consumed in moderation, Acetic Acid 80% is generally considered safe for consumption.

As consumers, it is important to stay informed about the presence of Acetic Acid 80% in our food products and make informed choices.
So, next time you come across the ingredient label with Acetic Acid 80%, rest assured that it can be embraced as a safe and effective addition to additive foods.



PROPERTIES OF ACETIC ACID 80%:
-Acetic Acid 80% crystals:

*Acidity
The hydrogen centre in the carboxyl group (−COOH) in carboxylic acids such as Acetic Acid 80% can separate from the molecule by ionization:
CH3COOH ⇌ CH3CO−2 + H+

Because of this release of the proton (H+), Acetic Acid 80% has acidic character.
Acetic Acid 80% is a weak monoprotic acid.
In aqueous solution, Acetic Acid 80% has a pKa value of 4.76.

Acetic Acid 80%'s conjugate base is acetate (CH3COO−).
A 1.0 M solution (about the concentration of domestic vinegar) has a pH of 2.4, indicating that merely 0.4% of the Acetic Acid 80% molecules are dissociated.
Only in very dilute (< 10−6 M) solution, Acetic Acid 80% is >90% dissociated.

*Deprotonation equilibrium of Acetic Acid 80% in water
Cyclic dimer of Acetic Acid 80%; dashed green lines represent hydrogen bonds



STRUCTURE OF ACETIC ACID 80%:
In solid Acetic Acid 80%, the molecules form chains of individual molecules interconnected by hydrogen bonds.
In the vapour phase at 120 °C (248 °F), dimers can be detected.

Dimers also occur in the liquid phase in dilute solutions with non-hydrogen-bonding solvents, and to a certain extent in pure Acetic Acid 80%, but are disrupted by hydrogen-bonding solvents.

The dissociation enthalpy of the dimer is estimated at 65.0–66.0 kJ/mol, and the dissociation entropy at 154–157 J mol−1 K−1.
Other carboxylic acids engage in similar intermolecular hydrogen bonding interactions.



SOLVENT PROPERTIES OF ACETIC ACID 80%:
Liquid Acetic Acid 80% is a hydrophilic (polar) protic solvent, similar to ethanol and water.
With a relative static permittivity (dielectric constant) of 6.2, Acetic Acid 80% dissolves not only polar compounds such as inorganic salts and sugars, but also non-polar compounds such as oils as well as polar solutes.

Acetic Acid 80% is miscible with polar and non-polar solvents such as water, chloroform, and hexane.
With higher alkanes (starting with octane), Acetic Acid 80% is not miscible at all compositions, and solubility of Acetic Acid 80% in alkanes declines with longer n-alkanes.

The solvent and miscibility properties of Acetic Acid 80% make it a useful industrial chemical, for example, as a solvent in the production of dimethyl terephthalate.



BIOCHEMISTRY OF ACETIC ACID 80%:
At physiological pHs, Acetic Acid 80% is usually fully ionised to acetate.
The acetyl group, formally derived from Acetic Acid 80%, is fundamental to all forms of life.
Typically, Acetic Acid 80% is bound to coenzyme A by acetyl-CoA synthetase enzymes, where it is central to the metabolism of carbohydrates and fats.

Unlike longer-chain carboxylic acids (the fatty acids), Acetic Acid 80% does not occur in natural triglycerides.
Most of the aceate generated in cells for use in acetyl-CoA is synthesized directly from ethanol or pyruvate.
However, the artificial triglyceride triacetin (glycerine triacetate) is a common food additive and is found in cosmetics and topical medicines; this additive is metabolized to glycerol and Acetic Acid 80% in the body.

Acetic Acid 80% is produced and excreted by Acetic Acid 80% bacteria, notably the genus Acetobacter and Clostridium acetobutylicum.
These bacteria are found universally in foodstuffs, water, and soil, and Acetic Acid 80% is produced naturally as fruits and other foods spoil.
Acetic Acid 80% is also a component of the vaginal lubrication of humans and other primates, where it appears to serve as a mild antibacterial agent.



PRODUCTION OF ACETIC ACID 80%:
Acetic Acid 80% is produced industrially both synthetically and by bacterial fermentation.
About 75% of Acetic Acid 80% made for use in the chemical industry is made by the carbonylation of methanol, explained below.

The biological route accounts for only about 10% of world production, but Acetic Acid 80% remains important for the production of vinegar because many food purity laws require vinegar used in foods to be of biological origin.
Other processes are methyl formate isomerization, conversion of syngas to Acetic Acid 80%, and gas phase oxidation of ethylene and ethanol.

Acetic Acid 80% can be purified via fractional freezing using an ice bath.
The water and other impurities will remain liquid while the Acetic Acid 80% will precipitate out.
As of 2003–2005, total worldwide production of virgin Acetic Acid 80% was estimated at 5 Mt/a (million tonnes per year), approximately half of which was produced in the United States.

European production was approximately 1 Mt/a and declining, while Japanese production was 0.7 Mt/a.
Another 1.5 Mt were recycled each year, bringing the total world market to 6.5 Mt/a.
Since then, the global production has increased from 10.7 Mt/a in 2010 to 17.88 Mt/a in 2023.


*Methanol carbonylation:
Most Acetic Acid 80% is produced by methanol carbonylation.
In this process, methanol and carbon monoxide react to produce Acetic Acid 80% according to the equation:
The process involves iodomethane as an intermediate, and occurs in three steps.
A metal carbonyl catalyst is needed for the carbonylation (step 2).

CH3OH + HI → CH3I + H2O
CH3I + CO → CH3COI
CH3COI + H2O → CH3COOH + HI

Two related processes exist for the carbonylation of methanol: the rhodium-catalyzed Monsanto process, and the iridium-catalyzed Cativa process.
The latter process is greener and more efficient and has largely supplanted the former process.

Catalytic amounts of water are used in both processes, but the Cativa process requires less, so the water-gas shift reaction is suppressed, and fewer by-products are formed.
By altering the process conditions, acetic anhydride may also be produced in plants using rhodium catalysis.


*Acetaldehyde oxidation:
Prior to the commercialization of the Monsanto process, most Acetic Acid 80% was produced by oxidation of acetaldehyde.
This remains the second-most-important manufacturing method, although Acetic Acid 80% is usually not competitive with the carbonylation of methanol.

The acetaldehyde can be produced by hydration of acetylene.
This was the dominant technology in the early 1900s.

Light naphtha components are readily oxidized by oxygen or even air to give peroxides, which decompose to produce Acetic Acid 80% according to the chemical equation, illustrated with butane:

2 C4H10 + 5 O2 → 4 CH3CO2H + 2 H2O
Such oxidations require metal catalyst, such as the naphthenate salts of manganese, cobalt, and chromium.

The typical reaction is conducted at temperatures and pressures designed to be as hot as possible while still keeping the butane a liquid.
Typical reaction conditions are 150 °C (302 °F) and 55 atm.
Side-products may also form, including butanone, ethyl acetate, formic acid, and propionic acid.

These side-products are also commercially valuable, and the reaction conditions may be altered to produce more of them where needed.
However, the separation of Acetic Acid 80% from these by-products adds to the cost of the process.
Similar conditions and catalysts are used for butane oxidation, the oxygen in air to produce Acetic Acid 80% can oxidize acetaldehyde.

2 CH3CHO + O2 → 2 CH3CO2H
Using modern catalysts, this reaction can have an Acetic Acid 80% yield greater than 95%.
The major side-products are ethyl acetate, formic acid, and formaldehyde, all of which have lower boiling points than Acetic Acid 80% and are readily separated by distillation.


*Ethylene oxidation
Acetaldehyde may be prepared from ethylene via the Wacker process, and then oxidised as above.
In more recent times, chemical company Showa Denko, which opened an ethylene oxidation plant in Ōita, Japan, in 1997, commercialised a cheaper single-stage conversion of ethylene to Acetic Acid 80%.

The process is catalyzed by a palladium metal catalyst supported on a heteropoly acid such as silicotungstic acid.
A similar process uses the same metal catalyst on silicotungstic acid and silica:

C2H4 + O2 → CH3CO2H
It is thought to be competitive with methanol carbonylation for smaller plants (100–250 kt/a), depending on the local price of ethylene.


*Oxidative fermentation:
For most of human history, Acetic Acid 80% bacteria of the genus Acetobacter have made Acetic Acid 80%, in the form of vinegar.
Given sufficient oxygen, these bacteria can produce vinegar from a variety of alcoholic foodstuffs.

Commonly used feeds include apple cider, wine, and fermented grain, malt, rice, or potato mashes.
The overall chemical reaction facilitated by these bacteria is:

C2H5OH + O2 → CH3COOH + H2O
A dilute alcohol solution inoculated with Acetobacter and kept in a warm, airy place will become vinegar over the course of a few months.
Industrial vinegar-making methods accelerate this process by improving the supply of oxygen to the bacteria.

The first batches of vinegar produced by fermentation probably followed errors in the winemaking process.
If must is fermented at too high a temperature, acetobacter will overwhelm the yeast naturally occurring on the grapes.

As the demand for vinegar for culinary, medical, and sanitary purposes increased, vintners quickly learned to use other organic materials to produce vinegar in the hot summer months before the grapes were ripe and ready for processing into wine.
This method was slow, however, and not always successful, as the vintners did not understand the process.

One of the first modern commercial processes was the "fast method" or "German method", first practised in Germany in 1823.
In this process, fermentation takes place in a tower packed with wood shavings or charcoal.

The alcohol-containing feed is trickled into the top of the tower, and fresh air supplied from the bottom by either natural or forced convection.
The improved air supply in this process cut the time to prepare vinegar from months to weeks.

Nowadays, most vinegar is made in submerged tank culture, first described in 1949 by Otto Hromatka and Heinrich Ebner.
In this method, alcohol is fermented to vinegar in a continuously stirred tank, and oxygen is supplied by bubbling air through the solution.
Using modern applications of this method, vinegar of 15% Acetic Acid 80% can be prepared in only 24 hours in batch process, even 20% in 60-hour fed-batch process.


*Anaerobic fermentation:
Species of anaerobic bacteria, including members of the genus Clostridium or Acetobacterium, can convert sugars to Acetic Acid 80% directly without creating ethanol as an intermediate.
The overall chemical reaction conducted by these bacteria may be represented as:

C6H12O6 → 3 CH3COOH
These acetogenic bacteria produce Acetic Acid 80% from one-carbon compounds, including methanol, carbon monoxide, or a mixture of carbon dioxide and hydrogen:

2 CO2 + 4 H2 → CH3COOH + 2 H2O
This ability of Clostridium to metabolize sugars directly, or to produce Acetic Acid 80% from less costly inputs, suggests that these bacteria could produce Acetic Acid 80% more efficiently than ethanol-oxidizers like Acetobacter.

However, Clostridium bacteria are less acid-tolerant than Acetobacter.
Even the most acid-tolerant Clostridium strains can produce vinegar in concentrations of only a few per cent, compared to Acetobacter strains that can produce vinegar in concentrations up to 20%.

At present, it remains more cost-effective to produce vinegar using Acetobacter, rather than using Clostridium and concentrating it.
As a result, although acetogenic bacteria have been known since 1940, their industrial use is confined to a few niche applications.



REACTIONS OF ACETIC ACID 80%:
Acetic Acid 80% undergoes the typical chemical reactions of a carboxylic acid.
Upon treatment with a standard base, Acetic Acid 80% converts to metal acetate and water.
With strong bases (e.g., organolithium reagents), Acetic Acid 80% can be doubly deprotonated to give LiCH2COOLi.

Reduction of Acetic Acid 80% gives ethanol.
The OH group is the main site of reaction, as illustrated by the conversion of Acetic Acid 80% to acetyl chloride.
Other substitution derivatives include acetic anhydride; this anhydride is produced by loss of water from two molecules of Acetic Acid 80%.

Esters of Acetic Acid 80% can likewise be formed via Fischer esterification, and amides can be formed.
When heated above 440 °C (824 °F), Acetic Acid 80% decomposes to produce carbon dioxide and methane, or to produce ketene and water:
CH3COOH → CH4 + CO2
CH3COOH → CH2=C=O + H2O



REACTIONS WITH INORGANIC COMPOUNDS OF ACETIC ACID 80%:
Acetic Acid 80% is mildly corrosive to metals including iron, magnesium, and zinc, forming hydrogen gas and salts called acetates:
Mg + 2 CH3COOH → (CH3COO)2Mg + H2

Because aluminium forms a passivating acid-resistant film of aluminium oxide, aluminium tanks are used to transport Acetic Acid 80%.
Containers lined with glass, stainless steel or polyethylene are also used for this purpose.
Metal acetates can also be prepared from Acetic Acid 80% and an appropriate base, as in the popular "baking soda + vinegar" reaction giving off sodium acetate:

NaHCO3 + CH3COOH → CH3COONa + CO2 + H2O
A colour reaction for salts of Acetic Acid 80% is iron(III) chloride solution, which results in a deeply red colour that disappears after acidification.
A more sensitive test uses lanthanum nitrate with iodine and ammonia to give a blue solution.
Acetates when heated with arsenic trioxide form cacodyl oxide, which can be detected by its malodorous vapours.



OTHER DERIVATIVES OF ACETIC ACID 80%:
Organic or inorganic salts are produced from Acetic Acid 80%.
Some commercially significant derivatives:
Sodium acetate, used in the textile industry and as a food preservative (E262).

Copper(II) acetate, used as a pigment and a fungicide.
Aluminium acetate and iron(II) acetate—used as mordants for dyes.
Palladium(II) acetate, used as a catalyst for organic coupling reactions such as the Heck reaction.

Halogenated Acetic Acid 80%s are produced from Acetic Acid 80%.
Some commercially significant derivatives:
ChloroAcetic Acid 80% (monochloroAcetic Acid 80%, MCA), dichloroAcetic Acid 80% (considered a by-product), and trichloroAcetic Acid 80%.

MCA is used in the manufacture of indigo dye.
BromoAcetic Acid 80%, which is esterified to produce the reagent ethyl bromoacetate.
TrifluoroAcetic Acid 80%, which is a common reagent in organic synthesis.
Amounts of Acetic Acid 80% used in these other applications together account for another 5–10% of Acetic Acid 80% use worldwide



STRUCTURE OF ACETIC ACID 80%:
It can be observed in the solid-state of Acetic Acid 80% that there is a chain of molecules wherein individual molecules are connected to each other via hydrogen bonds.
Dimers of ethanoic acid in Acetic Acid 80%'s vapour phase can be found at temperatures approximating to 120o

Even in the liquid phase of ethanoic acid, Acetic Acid 80%'s dimers can be found when it is present in a dilute solution.
These dimers are adversely affected by solvents that promote hydrogen bonding.

The structure of Acetic Acid 80% is given by CH3(C=O)OH, or CH3CO2H
Structurally, Acetic Acid 80% is the second simplest carboxylic acid (the simplest being formic acid, HCOOH), and is essentially a methyl group with a carboxyl functional group attached to it.



PREPARATION OF ACETIC ACID 80%:
Acetic Acid 80% is produced industrially via the carbonylation of methanol.
The chemical equations for the three steps involved in this process are provided below.
CH3OH (methanol) + HI (hydrogen iodide) → CH3I (methyl iodide intermediate) + H2O

CH3I + CO (carbon monoxide) → CH3COI (acetyl iodide)
CH3COI + H2O → CH3COOH (Acetic Acid 80%) + HI

Here, a methyl iodide intermediate is generated from the reaction between methanol and hydrogen iodide.
This intermediate is then reacted with carbon monoxide and the resulting compound is treated with water to afford the Acetic Acid 80% product.
It is important to note that a metal carbonyl complex must be used as a catalyst for step 2 of this process.



OTHER METHODS OF PREPARING ACETIC ACID 80%:
Some naphthalene salts of cobalt, chromium, and manganese can be employed as metal catalysts in the oxidation of acetaldehyde.
The chemical equation for this reaction can be written as:
O2 + 2CH3CHO → 2CH3COOH

Ethylene (C2H4) can be oxidized into Acetic Acid 80% with the help of a palladium catalyst and a heteropoly acid, as described by the following chemical reaction.
O2 + C2H4 → CH3COOH

Some anaerobic bacteria have the ability to directly convert sugar into Acetic Acid 80%.
C6H12O6 → 3CH3COOH
It can be noted that no ethanol intermediates are formed in the anaerobic fermentation of sugar by these bacteria.



PHYSICAL PROEPRTIES OF ACETIC ACID 80%:
Even though ethanoic acid is considered to be a weak acid, in its concentrated form, it possesses strong corrosive powers and can even attack the human skin if exposed to it.
Some general properties of Acetic Acid 80% are listed below.

Ethanoic acid appears to be a colourless liquid and has a pungent smell.
At STP, the melting and boiling points of ethanoic acid are 289K and 391K respectively.
The molar mass of Acetic Acid 80% is 60.052 g/mol and its density in the liquid form is 1.049 g.cm-3.

The carboxyl functional group in ethanoic acid can cause ionization of the compound, given by the reaction: CH3COOH ⇌ CH3COO– + H+
The release of the proton, described by the equilibrium reaction above, is the root cause of the acidic quality of Acetic Acid 80%.
The acid dissociation constant (pKa) of ethanoic acid in a solution of water is 4.76.

The conjugate base of Acetic Acid 80% is acetate, given by CH3COO–.
The pH of an ethanoic acid solution of 1.0M concentration is 2.4, which implies that it does not dissociate completely.
In its liquid form, Acetic Acid 80% is a polar, protic solvent, with a dielectric constant of 6.2.

The metabolism of carbohydrates and fats in many animals is centered around the binding of Acetic Acid 80% to coenzyme A.
Generally, this compound is produced via the reaction between methanol and carbon monoxide (carbonylation of methanol).



CHEMICAL PROPERTIES OF ACETIC ACID 80%:
The chemical reactions undergone by Acetic Acid 80% are similar to those of other carboxylic acids.
When heated to temperatures above 440oC, this compound undergoes decomposition to yield either methane and carbon dioxide or water and ethenone, as described by the following chemical equations.

CH3COOH + Heat → CO2 + CH4
CH3COOH + Heat → H2C=C=O + H2O
Some metals such as magnesium, zinc, and iron undergo corrosion when exposed to Acetic Acid 80%.
These reactions result in the formation of acetate salts.

2CH3COOH + Mg → Mg(CH3COO)2 (magnesium acetate) + H2
The reaction between ethanoic acid and magnesium results in the formation of magnesium acetate and hydrogen gas, as described by the chemical equation provided above.



OTHER REACTIONS OF ACETIC ACID 80%:
Acetic Acid 80% reacts with alkalis and forms acetate salts, as described below.
CH3COOH + KOH → CH3COOK + H2O
This compound also forms acetate salts by reacting with carbonates (along with carbon dioxide and water).
Examples of such reactions include:

2CH3COOH + Na2CO3 (sodium carbonate) → 2CH3COONa + CO2 + H2O
CH3COOH + NaHCO3 (sodium bicarbonate) → CH3COONa + CO2 + H2O
The reaction between PCl5 and ethanoic acid results in the formation of ethanoyl chloride.



WHAT ARE NATURAL SOURCES OF ACETIC ACID 80%?
Acetates (salts of Acetic Acid 80%) are common constituents of animal and plant tissues and are formed during the metabolism of food substances.
Acetate is readily metabolized by most tissues and may give rise to the production of ketones as intermediates.
Acetate is used by the body as a building block to make phospholipids, neutral lipids, steroids, sterols, and saturated and unsaturated fatty acids in a variety of human and animal tissue preparations.



KEY POINTS/OVERVIEW OF ACETIC ACID 80%:
One of the most common ways consumers may come into contact with Acetic Acid 80% is in the form of household vinegar, which generally contains about 5 percent Acetic Acid 80% and 95 percent water.

When Acetic Acid 80% is at 99.5 percent concentration, it is referred to a glacial Acetic Acid 80%, which can be used as raw material and solvent in the production of other chemical products.

Industrial applications of glacial Acetic Acid 80% include producing vinyl acetate, as solvent to dissolve oils, sulfur and iodine; acidizing oil and gas; manufacturing pharmaceuticals and vitamins, and food processing.



HOW ACETIC ACID 80% GETS INTO THE ENVIRONMENT:
Acetic Acid 80% can enter the environment from discharge and emissions from industries.
The burning of plastics or rubber, and exhaust fumes from vehicles may also release Acetic Acid 80% into the environment.
When released into soil Acetic Acid 80% evaporates into the air where it is broken down naturally by sunlight.
Levels of Acetic Acid 80% in the environment would be expected to be low.



PROPERTIES OF ACETIC ACID 80%:
Acetic Acid 80% is a smooth, colourless liquid with a 1 ppm visible, poisonous and destructive, unpleasant vinegar odour.
The melting point of Acetic Acid 80% is 16.73 ° C and the usual 117.9 ° C boiling point.
At 20°C, the density of pure Acetic Acid 80% is 1.0491.

It is highly hygroscopic Acetic Acid 80%.
It is possible to link the purity of the water solutions to their freezing point.
In carboxylic acids such as Acetic Acid 80%, the hydrogen centre in the carboxyl group −COOH can differentiate from the molecule by ionization:

Due to this proton H+1 release, Acetic Acid 80% has an acidic character.
Acetic Acid 80% is a weak monoprotic acid.
Acetic Acid 80% has a pK value of 4.76 in an aqueous solution.

Acetate CH3COO−1 is the conjugate base.
For polar and non-polar solvents such as acid, chloroform, and hexane, Acetic Acid 80% is miscible.
The molecules form chains in solid Acetic Acid 80%, with hydrogen bonds interconnecting individual molecules.

Dimers can be found in the vapour at 120 °C.
In the liquid form, dimers often exist in dilute solutions in non-hydrogen-bonding solvents and, to a certain degree, in pure Acetic Acid 80%; but are interacted with by solvents that bind to hydrogen.

Acetic Acid 80% is normally completely ionized to acetate at physiological phis.
Acetic Acid 80% is central to the metabolism of carbohydrates and fats when bound to coenzyme A.
Acetic Acid 80% does not exist in natural triglycerides, unlike longer-chain carboxylic acids (fatty acids).



DEHYDRATION OF ACETIC ACID 80%:
Dehydration of Acetic Acid 80% is one of the most important industrial uses of AD in the manufacture of aromatic acids such as terephthalic acid (TA), which involves a high purity of Acetic Acid 80%.

Two major parts are used in the manufacturing process: oxidation (where p-xylene is catalytically oxidized to produce crude TA) and PTA purification.
Acetic Acid 80%, present as a solvent in the oxidation reactor but also helpful to the reaction itself, must be isolated from the oxidation-produced water.

For the effective and economical operation of a TA facility, the recovery and storage of the Acetic Acid 80% solvent are important.
At high water temperatures, water, and Acetic Acid 80% show a pinch point, make recovering the pure acid very difficult.
Two absorbers (low and high pressure) and an acid dehydration column consist of a traditional Acetic Acid 80% recovery unit in a PTA phase.

Tall columns of 70–80 trays require the separation of Acetic Acid 80% and water by traditional distillation.
N-butyl acetate, which exhibits minimal miscibility with water and forms a heterogeneous azeotrope (b.p. 90.23°C), which is a typical azeotropic agent.
With all the water being fed to the dehydration column, n-Butyl acetate is added in appropriate amounts to form an azeotrope.

On condensation, the heterogeneous azeotrope forms two phases; an organic layer containing almost pure n-butyl acetate and an aqueous layer phase containing almost pure water.
The organic phase is recycled back to the column of dehydration, while the aqueous phase is fed to a column of stripping.
The amount of Acetic Acid 80% lost in the aqueous discharge is cut by approximately 40 per cent as AD results in a cleaner separation.



PHYSICAL and CHEMICAL PROPERTIES of ACETIC ACID 80%:
CAS: 64-19-7
Molecular Formula: C2H4O2
Molecular Weight (g/mol): 60.05
MDL Number: MFCD00036152
InChI Key: QTBSBXVTEAMEQO-UHFFFAOYSA-N
PubChem CID: 176
ChEBI: CHEBI:15366
IUPAC Name: acetic acid
SMILES: CC(O)=O
Linear Formula: CH3CO2H
Solubility Information: Solubility in water: completely soluble
Formula Weight: 60.05
Percent Purity: 80% (vol.)
Quantity: 5 L
Flash Point: >60°C
Chemical Name or Material: Acetic acid

Molecular Weight: 60.05 g/mol
XLogP3-AA: -0.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 0
Exact Mass: 60.021129366 g/mol
Monoisotopic Mass: 60.021129366 g/mol
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 4
Formal Charge: 0
Complexity: 31
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1

Compound Is Canonicalized: Yes
Chemical formula: CH3COOH
Molar mass: 60.052 g•mol−1
Appearance: Colourless liquid
Odor: Heavily vinegar-like
Density: 1.049 g/cm3 (liquid); 1.27 g/cm3 (solid)
Melting point: 16 to 17 °C; 61 to 62 °F; 289 to 290 K
Boiling point: 118 to 119 °C; 244 to 246 °F; 391 to 392 K
Solubility in water: Miscible
log P: -0.28
Vapor pressure: 1.54653947 kPa (20 °C); 11.6 mmHg (20 °C)
Acidity (pKa): 4.756
Conjugate base: Acetate
Magnetic susceptibility (χ): -31.54•10−6 cm3/mol
Refractive index (nD): 1.371 (VD = 18.19)
Viscosity: 1.22 mPa s; 1.22 cP
Dipole moment: 1.74 D

Thermochemistry
Heat capacity (C): 123.1 J K−1 mol−1
Std molar entropy (S⦵298): 158.0 J K−1 mol−1
Std enthalpy of formation (ΔfH⦵298): -483.88–483.16 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): -875.50–874.82 kJ/mol
Physical state: Liquid
Color: Colorless
Odor: Stinging
Melting point/freezing point: Melting point/range: 16.2 °C - lit.
Initial boiling point and boiling range: 117 - 118 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 19.9% (V),
Lower explosion limit: 4% (V)
Flash point: 39 °C - closed cup
Autoignition temperature: 463 °C
Decomposition temperature: Distillable in an undecomposed state at normal pressure.
pH: 2.5 at 50 g/L at 20 °C

Viscosity:
Kinematic viscosity: 1.17 mm2/s at 20 °C
Dynamic viscosity: 1.05 mPa•s at 25 °C
Water solubility: 602.9 g/L at 25 °C at 1.013 hPa - completely soluble
Partition coefficient (n-octanol/water): log Pow: -0.17 at 25 °C
Bioaccumulation is not expected.
Vapor pressure: 20.79 hPa at 25 °C
Density: 1.049 g/cm3 at 25 °C - lit.
Relative vapor density: 2.07
Surface tension: 28.8 mN/m at 10.0 °C
CAS number: 64-19-7
Molecular formula: C2H4O2
Molecular weight: 60.052 g/mol
Density: 1.1 ± 0.1 g/cm3
Boiling point: 117.1 ± 3.0 °C at 760 mmHg
Melting point: 16.2 °C (lit.)
Flash point: 40.0 ± 0.0 °C

EC index number: 607-002-00-6
EC number: 200-580-7
Hill Formula: C₂H₄O₂
Chemical formula: CH₃COOH
Molar Mass: 60.05 g/mol
HS Code: 2915 21 00
Boiling point: 116 - 118 °C (1013 hPa)
Density: 1.04 g/cm3 (25 °C)
Explosion limit: 4 - 19.9% (V)
Flash point: 39 °C
Ignition temperature: 485 °C
Melting Point: 16.64 °C
pH value: 2.5 (50 g/L, H₂O, 20 °C)
Vapor pressure: 20.79 hPa (25 °C)
Viscosity kinematic: 1.17 mm2/s (20 °C)

Solubility: 602.9 g/L soluble
Boiling point: 244°F
Molecular weight: 60.1
Freezing point/melting point: 62°F
Vapor pressure: 11 mmHg
Flash point: 103°F
Specific gravity: 1.05
Ionization potential: 10.66 eV
Lower explosive limit (LEL): 4.0%
Upper explosive limit (UEL): 19.9% at 200°F
NFPA health rating: 3
NFPA fire rating: 2
NFPA reactivity rating: 0
Alternative CAS RN: -
MDL Number: MFCD00036152
Storage Temperature: +20°C



FIRST AID MEASURES of ACETIC ACID 80%:
-Description of first-aid measures:
*General advice:
First aiders need to protect themselves.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water.
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of ACETIC ACID 80%:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up with liquid-absorbent and neutralising material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ACETIC ACID 80%:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ACETIC ACID 80%:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: butyl-rubber
Minimum layer thickness: 0,7 mm
Break through time: 480 min
Splash contact:
Material: Latex gloves
Minimum layer thickness: 0,6 mm
Break through time: 30 min
*Body Protection:
Flame retardant antistatic protective clothing.
*Respiratory protection:
Recommended Filter type: filter E-(P2)
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ACETIC ACID 80%:
-Precautions for safe handling:
*Advice on protection against fire and explosion:
Take precautionary measures against static discharge.
*Hygiene measures:
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities
*Storage conditions:
Keep container tightly closed in a dry and well-ventilated place.
Moisture sensitive.



STABILITY and REACTIVITY of ACETIC ACID 80%:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Incompatible materials:
No data available


ACETIC ACID FOOD GRADE
DESCRIPTION:

Acetic acid food grade systematically named ethanoic acid is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH (also written as CH3CO2H, C2H4O2, or HC2H3O2).
Vinegar is at least 4% Acetic acid food grade by volume, making Acetic acid food grade the main component of vinegar apart from water and other trace elements.
Acetic acid food grade is an organic compound with the formula CH3COOH.


CAS: 64-19-7


SYNONYMS OF ACETIC ACID FOOD GRADE:
Food Grade Acetic acid food grade, Ethanoic Acid, Vinegar Acid, Methane-carboxylic Acid,




Acetic acid food grade is a carboxylic acid consisting of a methyl group that is attached to a carboxyl functional group.
The systematic IUPAC name of Acetic acid food grade is ethanoic acid and its chemical formula can also be written as C2H4O2.
Vinegar is a solution of Acetic acid food grade in water and contains between 5% to 20% ethanoic acid by volume.

The pungent smell and the sour taste is characteristic of the Acetic acid food grade present in it.
An undiluted solution of Acetic acid food grade is commonly referred to as glacial Acetic acid food grade.
Acetic acid food grade forms crystals which appear like ice at temperatures below 16.6oC.

Acetic acid food grade has a wide range of applications as a polar, protic solvent.
In the field of analytical chemistry, glacial Acetic acid food grade is widely used in order to estimate substances that are weakly alkaline.

Acetic acid food grade, Food Grade is a colorless liquid with a strong pungent odor.
Acetic acid food grade is glacial Acetic acid food grade, the undiluted form of Acetic acid food grade.
Acetic acid food grade sds, sometimes called ethanoic acid or ethylic acid, is an organic acid and the simplest carboxylic acid. It is known for giving vinegar its sour taste and smell.

Though the ingredient is used in a wide range of fields, the oldest and most commonly known role of Acetic acid food grade is being the forerunner to vinegar.
When undiluted, it is known as Glacial Acetic acid food grade.












Glacial Acetic acid food grade, also known as ethanoic acid is an organic compound with the chemical formula of CH3COOH.
It is the main component of vinegar, which is typically made between 5% and 10% concentration mixed with water.
It has a distinctive sour taste and pungent smell.

Acetic acid food grade is used widely for descaling, as a chemical reagent and as a food additive.
In household uses it is often used in foods and cooking.
Glacial Acetic acid food grade Freezes at 62°F.

In lower concentrations with water, the freezing point lowers to below the freezing point of water.
As the solution becomes more heavily concentrated with water, it will freeze close to 32°F.
99.85+% Concentration, Freezes at 62°F





Acetic acid food grade is one of the simplest carboxylic acids. It is an important chemical reagent and is used in many staining procedures in a dilute form.


Glacial Acetic acid food grade, also known as ethanoic acid is an organic compound with the chemical formula of CH3COOH.
Acetic acid food grade is the main component of vinegar,

Acetic acid food grade has a distinctive sour taste and pungent smell.
Acetic acid food grade is used widely for descaling, as a chemical reagent and as a food additive.
In household uses it is often used in foods and cooking.


Acetic acid food grade (Food Grade) is a colourless, hygroscopic, and organic acid that can be used in many food applications.
Used as an antiseptic, Acetic acid food grade (Food Grade) is an antibacterial agent, disinfecting food preparation surfaces against staphylococci, streptococci, pseudomonas, enterococci, and other bacteria.

Considered as a weak acid, Acetic acid food grade (Food Grade) is mainly used as a preservative, acidulating agent, and flavouring agent for ice-creams, non-alcoholic beverages and baked goods.
It is one of the main volatile constituents of vinegar and pyroligneous acid.
In combination with leavening agents, it produces carbon dioxide from sodium bicarbonate.

This grade of Acetic acid food grade meets the requirements of the Food Chemical Codex and is produced under appropriate current good manufacturing practices for use as a food additive. Acetic acid food grade comes in different concentrations from 5 – 75% and sizes.



APPLICATIONS OF ACETIC ACID FOOD GRADE:
Acetic acid food grade is used as Artifical sweetener
Acetic acid food grade is used as Food flavors & food fragrances

Acetic acid food grade is used as Food ingredients
Acetic acid food grade is used as Food preservatives
Acetic acid food grade is used as Intermediates


Acetic acid food grade is used as Vinyl acetate monomer
Acetic acid food grade is used as Ester Production
Acetic acid food grade is used as Acetic Anhydride

Acetic acid food grade is used as Vinegar
Acetic acid food grade is used as solvent

Acetic acid food grade is used as Stop bath (development of Photographic films)
Acetic acid food grade is used as Descaling agents to remove limescale from taps and kettles.


Acetic acid food grade is used in food grade & ester production and it is also used as a solvent in various industrial applications.
A major use of Acetic acid food grade is for the production of vinyl acetate monomer (VAM) and also in food grade products.


Acetic acid food grade is the main component to vinegar, serving as 3% to 18% of vinegar’s volume by mass.
The rest of the solution is water.

Vinegar is typically used as a condiment, though it’s sometimes used a pickling agent in canned foods.
The ingredient changes the taste of foods, giving them a sour taste and odor.
The sour tang that is present in pickles, sourdough bread and sweet and sour chips come from glacial Acetic acid food grade.


Acetic acid food grade as an Antiseptic:
Glacial Acetic acid food grade can also be used as an antiseptic to disinfect food preparation surfaces.
The antibacterial properties kill staphylococci, streptococci and other bacteria.
The ingredient can even be used to treat certain infections that are not responding to antibiotics.

Acetic acid food grade is listed as an important medication by the World Health Organization (WHO) and has been used in medicine for hundreds of years.






Acetic acid food grade is used as an antiseptic due to its antibacterial qualities
The manufacture of rayon fiber involves the use of ethanoic acid.
Medically, Acetic acid food grade has been employed to treat cancer by its direct injection into the tumour.

Being the major constituent of vinegar, it finds use in the pickling of many vegetables.
The manufacture of rubber involves the use of ethanoic acid.
Acetic acid food grade is used as is also used in the manufacture of various perfumes.
Acetic acid food grade is used as is widely used in the production of VAM (vinyl acetate monomer).
When two molecules of Acetic acid food grade undergo a condensation reaction together, the product formed is acetic anhydride.


Acetic acid food grade applications include: manufacturing of acetic anhydride, cellulose acetate, and vinyl acetate monomer; acetic esters; chloroAcetic acid food grade; production of plastics, pharmaceuticals, dyes, insecticides, photographic chemicals; food additive; latex coagulant; oil-well acidizer; textile printing.


Glacial Acetic acid food grade has many uses.
Acetic acid food grade is used as is most often used as laboratory chemistry (PH regulator), food chemistry (production of sauces, processed cheese, salads) and industrial chemistry (fabric dyeing, production of artificial silk).

Its other uses:
Acetic acid food grade is used as rust remover;
Acetic acid food grade is used as descaling agent;
Acetic acid food grade is used as vinyl acetate monomer;

Acetic acid food grade is used as Production of esters;
Acetic acid food grade is used as acetic anhydride;
Acetic acid food grade is used as solvent;


Acetic acid food grade is used as Stop bath (developing photo films).
Due to its properties, Acetic acid food grade freezes below 16 ° C, assuming a solid form similar to ice crystals.







CHEMICAL AND PHYSICAL PROPERTIES OF ACETIC ACID FOOD GRADE:

Acetic acid food grade
99.85%
Water
00.15% Max
Colour
10 APHA Max
Formic Acid
0.05% Max . by wt.
Acetaldehyde
0.05% Max . by wt.
Heavy Metals as Pb
Less than 2 ppm
Iodides
40 ppb Max.
Permanganate
2.00 hrs.
min
Freezing point
16.4 deg C
Specific Gravity
1.049 at 25 deg C


SAFETY INFORMATION ABOUT ACETIC ACID FOOD GRADE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product
ACETIC ACID PROPYL ESTER
Acetic acid propyl ester (also known as 1-propyl acetate, propyl acetate, 1-acetoxypropane, acetic acid) is an organic compound with a molecular formula of C5H10O2 / CH3COOCH2CH2CH3.
Acetic acid propyl ester is commonly used as a solvent in coatings and printing inks.
Acetic acid propyl ester is highly flammable and Acetic acid propyl ester is abundantly miscible with all common organic solvents (alcohols, ketones, glycols, esters) but has only slight miscibility in water.

CAS Number: 109-60-4
EC Number: 203-686-1
Chemical Formula: CH3COOCH2CH2CH3
Molecular Weight: 102.13

Acetic acid propyl ester, also known as propyl ethanoate, is an organic compound.
Nearly 20,000 tons are produced annually for use as a solvent.

Acetic acid propyl ester is known by its characteristic odor of pears.
Due to this fact, Acetic acid propyl ester is commonly used in fragrances and as a flavor additive.
Acetic acid propyl ester is formed by the esterification of acetic acid and propan-1-ol, often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct.

Acetic acid propyl ester (also known as 1-propyl acetate, propyl acetate, 1-acetoxypropane, acetic acid) is an organic compound with a molecular formula of C5H10O2 / CH3COOCH2CH2CH3.
Acetic acid propyl ester is a clear, colourless ester that has a distinguishable acetate odour, is highly flammable, highly miscible with all common organic solvents (alcohols, ketones, glycols, esters) but only slightly miscible in water.

Acetic acid propyl ester appears as a clear colorless liquid with a pleasant odor.
Acetic acid propyl ester is flash point 58 °F.
Acetic acid propyl ester is less dense than water, Vapors are heavier than air.

Acetic acid propyl ester is an acetate ester obtained by the formal condensation of acetic acid with propanol.
Acetic acid propyl ester has a role as a fragrance and a plant metabolite.
Acetic acid propyl ester is functionally related to a propan-1-ol.

Acetic acid propyl ester is a clear, colourless liquid with a distinctive, pleasant fruity odour.
Acetic acid propyl ester is readily miscible with most organic solvents such as alcohol, ketones, glycols and esters, but Acetic acid propyl ester has only limited miscibility with water.

Acetic acid propyl ester is an organic compound with a molecular formula of C5H10O2.
Acetic acid propyl ester is a clear, colourless liquid that has a distinguishable acetate odor.

Acetic acid propyl ester is highly flammable and Acetic acid propyl ester is abundantly miscible with all common organic solvents (alcohols, ketones, glycols, esters) but has only slight miscibility in water.
Acetic acid propyl ester is commonly used as a solvent in coatings and printing inks.

Acetic acid propyl ester is an organic chemical compound, more specifically, an ester of acetic acid and propanol.
Acetic acid propyl ester is obtained by esterification of propanol with acetic acid in the presence of a catalyst.
Acetic acid propyl ester is also known as Propyl Ethanoate and is widely used as a solvent, but its characteristic odor makes Acetic acid propyl ester a fragrance as well.

Acetic acid propyl ester, also known as “propyl acetate” or “N-propyl acetate”, naturally exists in strawberries, bananas and tomatoes.
Acetic acid propyl ester is synthetically produced by having acetic acid and 1-propanol undergoing esterification reaction.

Acetic acid propyl ester is a colorless transparent liquid at room temperature with typical ester properties.
Acetic acid propyl ester has a special fruity odor and can be dissolved in both ethanol and ethyl ether.

Acetic acid propyl ester is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.
Acetic acid propyl ester is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Acetic acid propyl ester (also known as 1-propyl acetate) is an organic compound with a molecular formula of C5H10O2.
Acetic acid propyl ester is commonly used as a solvent in coatings and printing inks.

Acetic acid propyl ester is a clear, colourless liquid that has a distinguishable acetate odour.
Acetic acid propyl ester is highly flammable with a flash point of 14° C and a flammability rating of 3.
Acetic acid propyl ester is highly miscible with all common organic solvents (alcohols, ketones, glycols, esters) but has only slight miscibility in water.

Acetic acid propyl ester is a colorless, volatile solvent with an odor similar to acetone.
Acetic acid propyl ester has good solvency power for many natural and synthetic resins.
Acetic acid propyl ester is miscible with many organic solvents.

Acetic acid propyl ester is an ester with an average evaporation rate and high degree of solubility in the major resins on the market, such as nitrocellulose, and synthetic and natural resins.
Acetic acid propyl ester is used in formulations for paints and thinners for different applications, including printing inks (rotogravure and flexography), industrial coatings, original automotive paints and car refinishing.
In printing inks, Acetic acid propyl ester also stands out for its low retention in flexible polyethylene and polypropylene films.

Acetic acid propyl ester is a colorless, volatile solvent with an odor similar to acetone.
Acetic acid propyl ester has good solvency power for many natural and synthetic resins.
Acetic acid propyl ester is miscible with many organic solvents.

Acetic acid propyl ester is the propyl ester of acetic acid.

Acetic acid propyl ester, also known as 1-acetoxypropane or propyl ethanoate, belongs to the class of organic compounds known as carboxylic acid esters.
These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).

Acetic acid propyl ester exists as a clear, colourless liquid with fruity odor and has a bittersweet flavor reminiscent of pear on dilution.
Acetic acid propyl ester is commonly used in fragrances and as a flavor additive.
Its fruity aroma accounts for the aroma of passion fruit pulps (0.1% - 0.16% relative to total volatile compounds), melons, apples (4.57% - 9.89% relative to total aroma volatiles), and pears (1.31 mg/L in pear juice).

Acetic acid propyl ester is acts as a clear, colorless, volatile solvent for coatings, printing inks and chemical downstream industries.
Acetic acid propyl ester is possesses a characteristic odor reminiscent of acetone and a good solvent power for numerous natural and synthetic resins.

Acetic acid propyl ester is exhibits miscibility with many common solvents, e.g. alcohols, ketones, ethers, aldehydes, glycols and glycol ethers, but sparingly soluble in water.
Acetic acid propyl ester is used for coatings applications like wood lacquers and industrial finishes and for printing inks applications like flexographic and special screen inks.

Acetic acid propyl ester (nPAC) is an organic compound with the formula C5H10O2.
Acetic acid propyl ester is most used as solvent in lacquer, paint and chemistry industry.

Acetic acid propyl ester is a highly miscible organic solvent.
Acetic acid propyl ester is used in the production of fragrances and nail care products.

Acetic acid propyl ester is used as a solvent.
Acetic acid propyl ester plays an important role in the printing inks industry are flexographic and special screen printing inks.

Acetic acid propyl ester is widely used in fragrances and as a flavor additive due to its odor.
Acetic acid propyl ester acts as a good solvent for cellulose nitrate, acrylates, alkyd resins, rosin, plasticizers, waxes, oils and fats.

Acetic acid propyl ester is a chemical compound used as a solvent and an example of an ester.
Acetic acid propyl ester is known by its characteristic odor of pears.

Due to this fact, Acetic acid propyl ester is commonly used in fragrances and as a flavor additive.
Acetic acid propyl ester is formed by the esterification of acetic acid and 1-propanol (known as a condensation reaction), often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct.

Acetic acid propyl ester, also known as 1-acetoxypropane or propyl ethanoate, belongs to the class of organic compounds known as carboxylic acid esters.
These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
Based on a literature review very few articles have been published oAcetic acid propyl ester.

Acetic acid propyl ester, also known as propyl ethanoate, is an organic compound with a molecular formula of C5H10O2.
Acetic acid propyl ester is a clear and colourless liquid with with a mild fruity odor.

Acetic acid propyl ester is highly flammable with a flash point of 14°C and a flammability rating of 3.
Acetic acid propyl ester is highly miscible with all common organic solvents (alcohols, ketones, glycols, esters) but has only slight miscibility in water.

Acetic acid propyl ester is found in apple and formed by the esterification of acetic acid and 1-propanol (known as acondensation reaction), often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct.
Acetic acid propyl ester is primarily intended as a solvent in the coatings and printing inks industries.

Acetic acid propyl ester is widely used in fragrances and as a flavor additive due to its odor.
Acetic acid propyl ester also acts as a good solvent for cellulose nitrate, acrylates, alkyd resins, rosin, plasticizers, waxes, oils and fats.

Acetic acid propyl ester Market Outlook-2022-2032:
The global Acetic acid propyl ester market size is expected to reach a valuation of US$ 418.6 Mn by the end of 2022.
Sales of Acetic acid propyl ester are likely to expand at a CAGR of 5.4% from 2022 to 2032.

The global market is projected to top a valuation of US$ 706.3 Mn by the end of 2032.
Growing demand for Acetic acid propyl ester from the printing ink industry as a slow evaporation solvent is anticipated to drive the market during the projected period.

Acetic acid propyl ester, which is also known as propyl ethanoate, is an ester of acetic acid and n-propanol.
Acetic acid propyl ester is a clear, colorless liquid with a characteristic odor of peers and raspberry.

Acetic acid propyl ester is miscible with a wide variety of typical solvents, including alcohols, ketones, aldehydes, and glycol ethers, although in water Acetic acid propyl ester is only sparingly soluble.
Additionally, due to the presence of higher alkanes, Acetic acid propyl ester offers a slow rate of evaporation when used as an industrial solvent.

Owing to these characteristics, Acetic acid propyl ester is primarily implemented as a solvent for liquid, flexographic, and rotogravure printing inks.
In the cosmetics industry, Acetic acid propyl ester is used to make aerosol sprays, nail care products, cosmetics, and fragrances.

The growth of the Acetic acid propyl ester market is primarily driven by the printing ink industries.
Globally, these industries consume up to a one-third portion of the Acetic acid propyl ester and are expected to soar the demand in the forecast period.

The market for Acetic acid propyl ester is directly impacted by expansion in the printing ink sector.
The printing industry uses Acetic acid propyl ester extensively as a solvent, mostly for flexographic and screen printing inks.

Acetic acid propyl ester can thin a variety of different organic compounds, making Acetic acid propyl ester a useful solvent for this sector of the economy.
Particularly in emerging economies such as China and India, need for inks for paper media and packaging is surging.

The conventional ethyl acetate solvent in flexographic printing consumes more solvent, more ink, and requires flame retardants which hikes the printing costs.
However, with the use of Acetic acid propyl ester, high-quality flexography printings can be achieved with the consumption of 33% lesser solvent and 25% lesser ink which subsequently turns down the printing cost.
Thus, due to these improved benefits over ethyl acetate, Acetic acid propyl ester is quickly replacing Acetic acid propyl ester in the printing ink sector and will continue its growth in the forecast period.

Uses of Acetic acid propyl ester:
The major use of Acetic acid propyl ester is as a solvent in the coatings and printing industries.
Acetic acid propyl ester is a good solvent for these industries because Acetic acid propyl ester has the ability to thin many other organic compounds.

Acetic acid propyl ester dissolves a host of resins which make Acetic acid propyl ester a suitable solvent for wood lacquers and industrial finishes.
Within the printing industry Acetic acid propyl ester is mainly used in flexographic and special screening prints.

Acetic acid propyl ester is also used in aerosol sprays, nail care and as a fragrance solvent.
Acetic acid propyl ester can also be used as a flavouring additive due to its odour similar to pears.
The main user end markets are the printing, coatings, lacquers, cosmetic and flavouring industries.

Acetic acid propyl ester is used as a solvent, flavoring agent, and chemical intermediate.

Acetic acid propyl ester is flavoring agents, perfumery, solvent for nitrocellulose and other cellulose derivatives, natural and synthetic resins, lacquers, plastics, organic synthesis, lab reagent
Acetic acid propyl ester is a powerful solvent and is used in waxes, and insecticide formulations.

Acetic acid propyl ester is used in alcohol-dilutable inks containing nitrocellulose as a main constituent, polyamide inks, acrylic inks.

Widespread uses by professional workers:
Acetic acid propyl ester is used in the following products: coating products, laboratory chemicals, lubricants and greases, washing & cleaning products, inks and toners and metal working fluids.
Acetic acid propyl ester is used in the following areas: building & construction work and scientific research and development.

Acetic acid propyl ester is used for the manufacture of: , fabricated metal products, electrical, electronic and optical equipment and machinery and vehicles.
Other release to the environment of Acetic acid propyl ester is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids) and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).

Uses at industrial sites:
Acetic acid propyl ester is used in the following products: coating products, washing & cleaning products, inks and toners, lubricants and greases and metal working fluids.
Acetic acid propyl ester has an industrial use resulting in manufacture of another substance (use of intermediates).

Acetic acid propyl ester is used for the manufacture of: chemicals.
Release to the environment of Acetic acid propyl ester can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and of substances in closed systems with minimal release.

Industry Uses:
Intermediate
Not Known or Reasonably Ascertainable
Other
Other (specify)
Paint additives and coating additives not described by other categories
Pigments
Solvent

Consumer Uses:
Acetic acid propyl ester is used in the following products: lubricants and greases, coating products, anti-freeze products, perfumes and fragrances, adhesives and sealants, washing & cleaning products, leather treatment products, cosmetics and personal care products and polishes and waxes.
Other release to the environment of Acetic acid propyl ester is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids) and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).

Other Consumer Uses:
Not Known or Reasonably Ascertainable
Paint additives and coating additives not described by other categories
Pigments
Solvent

Industrial Processes with risk of exposure:
Painting (Solvents)
Plastic Composites Manufacturing

Applications of Acetic acid propyl ester:
Acetic acid propyl ester is mainly used as a solvent in the industrial production of coatings and printing inks (owing to its suitability to thin down many other organic compounds).
Acetic acid propyl ester is also an excellent solvent for many natural and synthetic resins (such as cellulose nitrate, acrylates, colophony, plastifiers, wax, oils and fats), varnishes for wood, natural and synthetic dyes and plastics.
Acetic acid propyl ester is also used to produce insecticides and in the perfume, printing and food industry (as a flavor additive for food lending Acetic acid propyl ester the taste and flavor of a pear).

Acetic acid propyl ester mainly used as solvent in printing inks, especially in flexographic and special screen printing inks, also used as a safe and pro-environment solvent for food package printing ink industry and used in PTA(purified tereph-thalic acid) industry.
With strong ability to dissolve many natural and synthetic resins (e.g. cellulose nitrate, acrylates, alkyd resin) Coatings for automotive and plastic Solvents for cosmetics and personal care, for fragrances.

Acetic acid propyl ester is used as an active solvent in many ink and coating applications.
For cosmetics and personal care, Acetic acid propyl ester can be used in nail care or as a flavoring agent.
In addition, Acetic acid propyl ester has been listed as Inert Ingredients Permitted for Use in Nonfood Use Pesticide Products under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA).

Acetic acid propyl ester is used as a solvent.
Acetic acid propyl ester plays an important role in the printing inks industry are flexographic and special screen printing inks.

Acetic acid propyl ester is widely used in fragrances and as a flavor additive due to its odor.
Acetic acid propyl ester acts as a good solvent for cellulose nitrate, acrylates, alkyd resins, rosin, plasticizers, waxes, oils and fats.

Acetic acid propyl ester is primarily used as a solvent in the manufacture of paints and coatings because of its ability to thin many other organic compounds.
Acetic acid propyl ester has the power to dissolve a wide range of resins, which also makes Acetic acid propyl ester highly suitable as a solvent for wood lacquers and industrial finishes.

Acetic acid propyl ester is widely used in the printing industry, mainly for flexographic and screen printing inks.
Acetic acid propyl ester is also used as a solvent in perfumes and is found as an ingredient in aerosol sprays, nail care products and cosmetics.

Acetic acid propyl ester is used as an intermediate in organic chemistry of pharmaceutical compounds.
Acetic acid propyl ester is also used as a flavouring additive on account of its fruity odour, which is similar to pears.

Other Applications:
Coatings
Wood lacquers
Aerosol sprays
Nail care
Cosmetic / personal care solvent
Fragrance solvent
Process solvent
Printing inks (especially flexographic and special screen)

Features of Acetic acid propyl ester:
Acetic acid propyl ester’s main application is in the printing inks industry for flexographic and special screen printing inks.
Acetic acid propyl ester is slightly soluble in water but is miscible with alcohols, ketones, esters and hydrocarbons.
Acetic acid propyl ester is a suitable fluid for blended products requiring variation in end-use performance.

Other Features:
Clear, highly volatile liquid
Mild odor
Sparingly soluble in water
Good resin solvent
Slow RER
Promotes flow and leveling
Non-HAP (Hazardous Air Pollutant) Solvent
Solvency power similar to ethyl acetate
Miscible with many organic solvents (alcohols, ketones, aldehydes, glycols and glycol ethers)

Manufacturing Methods of Acetic acid propyl ester:
Acetic acid propyl ester is produced by direct esterification of the corresponding alcohol with acetic acid in the presence of sulfuric acid, ptoluenesulfonic acid, methanesulfonic acid, or a strong cationic resin as catalyst.
1-Propanol can also undergo ester interchange with methyl or ethyl acetate in the presence of a strong cationic exchange resin to give Acetic acid propyl ester.

Acetic acid propyl ester is manufacture from acetic acid and mixture of propene and propane in the presence of zinc chloride catalyst.
Acetic acid propyl ester is manufacture from interaction of acetic acid and n-propyl alcohol in the presence of sulfuric acid.

Typical Properties of Acetic acid propyl ester:

Chemical Properties:
Acetic acid propyl ester has a fruity (pear–raspberry) odor with a pleasant, bittersweet flavor reminiscent of pear on dilution.
The Odor Threshold is 70 milligram per cubic meter and 2.8 milligram per cubic meter (New Jersey Fact Sheet).

Physical properties:
Clear, colorless, flammable liquid with a pleasant, pear-like odor.
Experimentally determined detection and recognition odor threshold concentrations were 200 μg/m3 (48 ppbv) and 600 μg/m3 (140 ppbv), respectively.

An odor threshold concentration of 240 ppbv was determined by a triangular odor bag method.
Cometto-Mu?iz and Cain (1991) reported an average nasal pungency threshold concentration of 17,575 ppmv.

General Manufacturing Information of Acetic acid propyl ester:

Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
Miscellaneous Manufacturing
Non-metallic Mineral Product Manufacturing (includes clay, glass, cement, concrete, lime, gypsum, and other non-metallic mineral product manufacturing)
Not Known or Reasonably Ascertainable
Oil and Gas Drilling, Extraction, and Support activities
Paint and Coating Manufacturing
Pharmaceutical and Medicine Manufacturing
Plastics Material and Resin Manufacturing
Printing Ink Manufacturing
Printing and Related Support Activities
Synthetic Dye and Pigment Manufacturing

Human Metabolite Information of Acetic acid propyl ester:

Cellular Locations:
Cytoplasm
Extracellular

Handling and Storage of Acetic acid propyl ester:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling Acetic acid propyl ester must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Acetic acid propyl ester without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Storage and Handling of Acetic acid propyl ester:
Acetic acid propyl ester should be stored in a tightly-closed containerin a cool, dry, well-ventilated place away from direct sunlight, heat, sources of ignition and incompatible materials such as strong oxidizers, acids and bases.
Containers which have been opened should be carefully resealed and stored in an upright position to avoid leakage.

Handle in accordance with good industry practices for safety and hygiene.
Personal protective equipment including eye goggles and impermeable gloves and clothing should be worn to avoid contact with skin and eyes.
Appropriate engineering controls including sufficient natural or exhaust ventilation must be implemented and respiratory protection should be worn to prevent exposure to vapours.

Reactivity Profile of Acetic acid propyl ester:
Acetic acid propyl ester is an ester.
Acetic acid propyl ester is colorless, highly flammable liquid, moderately toxic.

Dangerous fire hazard when exposed to heat, flame, sparks, or strong oxidizers.
When heated to decomposition Acetic acid propyl ester emits acrid smoke and irritating fumes.

First Aid Measures of Acetic acid propyl ester:

Eye:
IRRIGATE IMMEDIATELY - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids.
Get medical attention immediately.

Skin:
WATER FLUSH PROMPTLY - If this chemical contacts the skin, flush the contaminated skin with water promptly.
If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water promptly.
If irritation persists after washing, get medical attention.

Breathing:
RESPIRATORY SUPPORT - If a person breathes large amounts of this chemical, move the exposed person to fresh air at once.
If breathing has stopped, perform artificial respiration.

Keep the affected person warm and at rest.
Get medical attention as soon as possible.

Swallow:
MEDICAL ATTENTION IMMEDIATELY - If this chemical has been swallowed, get medical attention immediately.

Fire Fighting of Acetic acid propyl ester:

CAUTION:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.
Do not use dry chemical extinguishers to control fires involving nitromethane (UN1261) or nitroethane (UN2842).

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto the product.
If Acetic acid propyl ester can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

For massive fire, use unmanned master stream devices or monitor nozzles.
If this is impossible, withdraw from area and let fire burn.

Use alcohol-resistant foam, foam, powder, carbon dioxide, fine water spray.
In case of fire: keep drums, etc., cool by spraying with water.

Fire Fighting Procedures of Acetic acid propyl ester:

If material on fire or involved in fire:
Do not extinguish fire unless flow can be stopped or safely confined.
Use water in flooding quantities of fog.

Solid streams of water may be ineffective.
Cool all affected containers with flooding quantities of water.

Apply water from as far a distance as possible.
Use "alcohol foam, dry chemical or carbon dioxide.

Accidental Release Measures of Acetic acid propyl ester:

Isolation and Evacuation:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Spillage Disposal of Acetic acid propyl ester:
Remove all ignition sources.
Evacuate danger area!

Consult an expert! Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of the substance.
Do NOT wash away into sewer.

Do NOT let this chemical enter the environment.
Collect leaking liquid in sealable containers.

Absorb remaining liquid in sand or inert absorbent.
Then store and dispose of according to local regulations.

Disposal Methods of Acetic acid propyl ester:
The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
Recycle any unused portion of Acetic acid propyl ester for its approved use or return Acetic acid propyl ester to the manufacturer or supplier.

Ultimate disposal of the chemical must consider:
Acetic acid propyl ester's impact on air quality; potential migration in soil or water; effects on animal and plant life; and conformance with environmental and public health regulations.

Preventive Measures of Acetic acid propyl ester:
The scientific literature for the use of contact lenses by industrial workers is inconsistent.
The benefits or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses.

However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye.
In those specific cases, contact lenses should not be worn.
In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Identifiers of Acetic acid propyl ester:
CAS Number: 109-60-4
ChEBI: CHEBI:40116
ChEMBL: ChEMBL44857
ChemSpider: 7706
DrugBank: DB01670
ECHA InfoCard: 100.003.352
EC Number: 203-686-1
PubChem CID: 7997
RTECS number: AJ3675000
UNII: 4AWM8C91G6
UN number: 1276
CompTox Dashboard (EPA): DTXSID6021901
InChI: InChI=1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3
Key: YKYONYBAUNKHLG-UHFFFAOYSA-N
InChI=1/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3
Key: YKYONYBAUNKHLG-UHFFFAOYAC
SMILES: O=C(OCCC)C

CAS number: 109-60-4
EC index number: 607-024-00-6
EC number: 203-686-1
Hill Formula: C₅H₁₀O₂
Chemical formula: CH₃COOCH₂CH₂CH₃
Molar Mass: 102.13 g/mol
HS Code: 2915 39 00

Synonyms: Propyl acetate
Linear Formula: CH3COOCH2CH2CH3
CAS Number: 109-60-4
Molecular Weight: 102.13

Molecular Weight:102.13200
Exact Mass:102.13
EC Number:203-686-1
UNII:4AWM8C91G6
ICSC Number:0940
NSC Number:72025
UN Number:1276
DSSTox ID:DTXSID6021901
Color/Form:Colorless liquid
HScode:2915390090

CAS: 109-60-4
Molecular Formula: C5H10O2
Molecular Weight (g/mol): 102.13
MDL Number: MFCD00009372
InChI Key: YKYONYBAUNKHLG-UHFFFAOYSA-N
PubChem CID: 7997
ChEBI: CHEBI:40116
IUPAC Name: propyl acetate
SMILES: CCCOC(C)=O

Linear Formula: CH3COOCH2CH2CH3
CAS Number: 109-60-4
Molecular Weight: 102.13
Beilstein: 1740764
EC Number: 203-686-1
MDL number: MFCD00009372
eCl@ss: 39022103
PubChem Substance ID: 329757979
NACRES: NA.21

Boiling point: 101.5 °C (1013 hPa)
Density: 0.89 g/cm3 (20 °C)
Explosion limit: 1.7 - 8 %(V)
Flash point: 11.8 °C
Ignition temperature: 430 °C
Melting Point: -95 °C
Vapor pressure: 33 hPa (20 °C)
Solubility: 21.2 g/l

Properties of Acetic acid propyl ester:
Chemical formula: C5H10O2
Molar mass: 102.133 g·mol−1
Appearance: Colorless liquid
Odor: Mild, fruity
Density: 0.89 g/cm3
Melting point: −95 °C (−139 °F; 178 K)
Boiling point: 102 °C (216 °F; 375 K)
Solubility in water: 18.9 g/L
Vapor pressure: 25 mmHg (20 °C)
Magnetic susceptibility (χ): −65.91·10−6 cm3/mol

PSA:26.30000
XLogP3:0.9595
Appearance:Colorless liquid with a strong odor
Density:0.836 g/cm3 @ Temp: 20 °C
Melting Point:-93 °C
Boiling Point:101.5 °C @ Press: 760 Torr
Flash Point:55 °F
Refractive Index:n20/D 1.384(lit.)
Water Solubility:H2O: 2g/100 mL (20 ºC)
Storage Conditions:Storage Room low temperature ventilation drying ,Separate storage with oxidizing agent
Vapor Pressure:35.2mmHg at 25°C
Vapor Density:3.5 (vs air)
Flammability characteristics:Class IB Flammable Liquid: Fl.P. below 73°F and BP at or above 100°F.
Explosive limit:vol% in air: 1.7.0
Odor:Pleasant odor
Taste:Pleasant, bittersweet flavor reminiscent of pear on dilution.
OH:3.40e-12 cm3/molecule*sec
Henrys Law Constant:2.18e-04 atm-m3/mole|Henry's Law constant = 2.18X10-4 atm-cu m/mol at 25 °C
Air and Water Reactions:Highly flammable. Slightly soluble in water.

Molecular Formula: C5H10O2 / CH3COOCH2CH2CH3
Cas Number: 109-60-4
Molecular Mass: 102.06808 g/mol
Flashpoint: 58 °F / 14.4 °C
Boiling Point: 214.9 ° F at 760 mm Hg
Melting Point: -139 °F / -95 °C
Vapour Pressure: 67.21 mm Hg
Water Solubility: g/100ml at 16 °C: 1.6
Density: 0.886 at 68 °F

vapor density: 3.5 (vs air)
Quality Level: 200
vapor pressure: 25 mmHg ( 20 °C)
Assay: ≥99.5%
form: liquid
autoignition temp.: 842 °F

expl. lim.:
1.7 %, 37 °F
8 %

impurities:
≤0.01% Acetic acid (free acid)
≤0.1% Water

evapn. residue: ≤0.01%
color: APHA: ≤15
refractive index: n20/D 1.384 (lit.)
bp: 102 °C (lit.)
mp: −95 °C (lit.)
density: 0.888 g/mL at 25 °C (lit.)
SMILES string: CCCOC(C)=O
InChI: 1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3
InChI key: YKYONYBAUNKHLG-UHFFFAOYSA-N

Molecular Weight: 102.13 g/mol
XLogP3: 1.2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 3
Exact Mass: 102.068079557 g/mol
Monoisotopic Mass: 102.068079557 g/mol
Topological Polar Surface Area: 26.3Ų
Heavy Atom Count: 7
Complexity: 59.1
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Acetic acid propyl ester:
Melting Point: -92°C
Density: 0.887
Boiling Point: 99°C to 102°C
Flash Point: 14°C (57°F)
Odor: Fruit-like
Linear Formula: CH3CO2CH2CH2CH3
Refractive Index: 1.384
Quantity: 500 mL
UN Number: UN1276
Beilstein: 1740764
Merck Index: 14,7841
Solubility Information: Miscible with alcohols,ketones,aldehydes,ethers,glycols and glycol ethers. Slightly soluble in water.
Formula Weight: 102.13
Percent Purity: 99%
Chemical Name or Material: Acetic acid propyl ester

Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 0.886 - 0.888
Identity (IR): passes test

Related compounds of Acetic acid propyl ester:
Propan-1-ol
Acetic acid

Related esters:
Ethyl acetate
Isopropyl acetate
n-butyl acetate
Isobutyl acetate

Names of Acetic acid propyl ester:

Regulatory process names:
1-Acetoxypropane
1-Propyl acetate
Acetate de propyle normal
Acetic acid n-propyl ester
Acetic acid, propyl ester
n-PROPYL ACETATE
n-Propyl acetate
n-Propyl acetate (natural)
n-Propyl ethanoate
Octan propylu
Propyl acetate
Propyl acetate
propyl acetate
Propyl ethanoate
Propylester kyseliny octove

Translated names:
acetat de propil (mt)
acetat de propil (ro)
acetato de propilo (es)
acetato de propilo (pt)
acetato di propile propilacetato (it)
acétate de propyle; (fr)
octan propylu (pl)
propil acetat (sl)
propil-acetát (hu)
propilacetatas (lt)
propilacetāts (lv)
propyl-acetát (cs)
propyl-acetát (sk)
propylacetaat (nl)
propylacetat (da)
Propylacetat (de)
propylacetat (no)
propylacetat (sv)
Propyyliasetaatti (fi)
propüülatsetaat (et)
οξικός προπυλεστέρας (el)
пропил ацетат (bg)

IUPAC names:
Acetic acid, propyl ester
Acetic acid, propylester
EC_203_686_1__propyl_acetate
n-propyl acetate
n-Propyl ethanoate
n-propyl ethanoate
NPAC
PROPYL ACETATE
Propyl Acetate
Propyl acetate
propyl acetate
Propyl Acetate
Propyl acetate
propyl acetate
PROPYL ACETATE, NORMAL
Propyl ethanoate
propyl ethanoate
propylacetate

Preferred IUPAC name:
Propyl acetate

Systematic IUPAC name:
Propyl ethanoate

Trade names:
1-Acetoxypropane
1-Propyl acetate
ACETATE, PROPYL
Acetic acid n-propyl ester
acetic acid propyl ester
Acetic acid, propyl ester
ESSIGSAEURE-PROPYLESTER
n-Propanol acetate
n-Propyl Acetate
n-Propyl acetate
n-propyl acetate
n-Propylacetat
NSC 72025
Pr acetate
propyl acetate
Propyl ethanoate
Propylacetat

Other names:
Acetic acid propyl ester
n-Propyl ethanoate
n-Propyl acetate
n-Propyl ester of acetic acid

Other identifiers:
109-60-4
607-024-00-6

Synonyms of Acetic acid propyl ester:
Propyl acetate
109-60-4
N-PROPYL ACETATE
Acetic acid, propyl ester
Propyl ethanoate
1-Acetoxypropane
1-Propyl acetate
n-Propyl ethanoate
Octan propylu
Acetic acid n-propyl ester
Propylacetate
Acetate de propyle normal
n-Propyl acetate (natural)
Acetic acid propyl ester
FEMA No. 2925
Propylester kyseliny octove
NSC 72025
HSDB 161
Octan propylu [Polish]
n-propanol acetate
EINECS 203-686-1
Acetic acid, n-propyl ester
UNII-4AWM8C91G6
BRN 1740764
4AWM8C91G6
DTXSID6021901
CHEBI:40116
AI3-24156
Acetate de propyle normal [French]
Propylester kyseliny octove [Czech]
NSC-72025
UN1276
DTXCID301901
ACETIC ACID,PROPYL ESTER
EC 203-686-1
4-02-00-00138 (Beilstein Handbook Reference)
PROPYL ACETATE (USP-RS)
PROPYL ACETATE [USP-RS]
n-propylacetat
n-Propyl ester of acetic acid
?Propyl acetate
acetic acid propyl
Propyl acetate, N-
ACETATE, PROPYL
Propyl acetate, 99%
PAT (CHRIS Code)
Actate de propyle normal
CH3COOCH2CH2CH3
Acetic acid-n-propyl ester
Propyl ester of acetic acid
PROPYL ACETATE [MI]
FEMA NUMBER 2935
SCHEMBL14991
PROPYL ACETATE [FCC]
WLN: 3OV1
CHEMBL44857
PROPYL ACETATE [FHFI]
PROPYL ACETATE [INCI]
Propyl acetate, >=99.5%
Propyl acetate, >=98%, FG
N-PROPYL ACETATE [HSDB]
N-Propyl acetate LBG-64752
Propyl acetate, analytical standard
ACETIC ACID, N-PROPYL ETHER
NSC72025
Tox21_202012
MFCD00009372
NA1276
STL280317
AKOS008949448
DB01670
LS-3066
UN 1276
NCGC00249148-01
NCGC00259561-01
CAS-109-60-4
A0044
FT-0621756
FT-0627474
Propyl acetate, natural, >=97%, FCC, FG
n-Propyl acetate [UN1276] [Flammable liquid]
n-Propyl acetate [UN1276] [Flammable liquid]
Q415750
J-002310
InChI=1/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H
Propyl acetate, United States Pharmacopeia (USP) Reference Standard
Propyl Acetate, Pharmaceutical Secondary Standard; Certified Reference Material
109-60-4 [RN]
203-686-1 [EINECS]
Acétate de propyle [French] [ACD/IUPAC Name]
Acetic acid n-propyl ester
Acetic acid, n-propyl ester
Acetic acid, propyl ester [ACD/Index Name]
MFCD00009372 [MDL number]
n-propyl acetate
n-Propyl ethanoate
Propyl acetate [ACD/IUPAC Name]
Propyl ethanoate
Propyl-acetat [German] [ACD/IUPAC Name]
Propylester kyseliny octove [Czech]
1-Propyl acetate
3OV1 [WLN]
4-02-00-00138 (Beilstein Handbook Reference) [Beilstein]
4PA
ACETIC ACID PROPYL ESTER
Acetic acid-n-propyl ester
NORMAL PROPYL ACETATE
N-PROPANOL ACETATE
Octan propylu
Trimethylene acetate
WLN: 3OV1
ACETONE
SYNONYMS Ethanoyl chloride; Acetic acid chloride; CAS NO. 75-36-5
ACETONE

Acetone is a colorless, volatile, and flammable organic compound with the chemical formula C3H6O.
Acetone is the simplest and smallest ketone, consisting of a carbonyl group (C=O) bonded to two methyl groups (-CH3).
Acetone is highly miscible with water, alcohol, and other organic solvents, making it a versatile solvent widely used in various industries and everyday applications.

CAS number: 67-64-1
EC number: 200-662-2



APPLICATIONS


Acetone is widely used as a solvent in industries such as paint, coatings, and adhesives.
Acetone is a common ingredient in nail polish removers, effectively dissolving and removing nail polish.

Acetone finds applications in the pharmaceutical industry as a solvent for active ingredients and excipients.
Acetone is used in the synthesis of various chemicals, including methyl methacrylate and bisphenol-A.

Acetone is a valuable cleaning agent and degreaser, widely used in industrial settings.
Acetone is used in the formulation of paints, varnishes, and lacquers, aiding in their proper consistency.
Acetone is utilized in the production of printing inks, helping to dissolve ink components.

Acetone is employed in the extraction of natural products, such as essential oils from plants.
Acetone is used in the formulation of personal care products like perfumes and lotions.

Acetone is utilized in laboratories for various analytical and research purposes.
Acetone is involved in the production of synthetic fibers like rayon and acetate.

Acetone finds applications in the rubber industry, aiding in the extraction and processing of rubber.
Acetone is used in the formulation of adhesives and sealants, facilitating effective bonding.
Acetone is involved in the cleaning and degreasing of electronic components and printed circuit boards.

Acetone is utilized in the automotive industry for cleaning and degreasing auto parts and engines.
Acetone finds applications in analytical chemistry techniques such as chromatography and spectrophotometry.

Acetone is used in the formulation of toners and astringents in the cosmetics and skincare industry.
Acetone is involved in the cleaning of printing plates and removal of inks in the printing industry.

Acetone is used in the production of certain agrochemicals, including pesticides and herbicides.
Acetone finds applications in the production of surface coatings and laminates, such as automotive paints.
Acetone is used in the metalworking industry for cleaning and degreasing metal surfaces.

Acetone is employed as a solvent in the formulation of cleaning agents and household products.
Acetone is used in the production of fiberglass and composite materials.

Acetone finds applications in the production of synthetic rubber and plastic materials.
Acetone is involved in the formulation of solvents and cleaning solutions for various applications.

Acetone is used as a solvent for removing epoxy and resin-based adhesives.
Acetone finds applications in the cleaning and maintenance of glassware and laboratory equipment.
Acetone is employed in the formulation of paint strippers and graffiti removers.

Acetone is used in the production of composite materials, such as carbon fiber-reinforced plastics.
Acetone is involved in the formulation of industrial coatings and protective finishes.

Acetone finds applications in the production of foam plastics and polyurethane materials.
Acetone is used in the manufacturing of electronic components and printed circuit boards.

Acetone finds applications in the formulation of cleaning solutions for optical lenses and camera equipment.
Acetone is used in the recycling and recovery of certain plastics and polymers.
It is employed in the synthesis of various pharmaceutical intermediates and active ingredients.

Acetone finds applications in the production of rubber and polymer-based sealants and gaskets.
Acetone is used in the formulation of rapid-drying inks and markers.

Acetone is involved in the production of solvents for cellulose-based materials, such as cellophane.
Acetone finds applications in the cleaning and maintenance of 3D printing equipment and surfaces.

Acetone is used as a solvent for cleaning and degreasing precision instruments and mechanical parts.
Acetone is employed in the production of solvents and solutions for industrial parts cleaning and degreasing.
Acetone finds applications in the formulation of solvents for the removal of graffiti and paint stains.

Acetone is used in the production of rubber and plastic-based adhesives.
Acetone is involved in the formulation of coatings for metal surfaces, providing protection against corrosion.

Acetone finds applications in the production of personal protective equipment (PPE), such as gloves and goggles.
Acetone is used in the formulation of solvents for removing ink and dye stains from fabrics and textiles.

Acetone is employed in the production of automotive cleaning and maintenance products, including carburetor cleaners and brake cleaners.
Acetone finds applications in the formulation of solvents for cleaning and degreasing firearms and weapons.

Acetone is used in the production of solvents for cleaning and maintenance of aircraft and aerospace components.
Acetone is involved in the formulation of solvents for the cleaning and degreasing of marine equipment and surfaces.


Acetone has a wide range of applications across various industries.
Some of its key applications include:

Solvent:
Acetone is widely used as a solvent in many industries, including paint, coatings, varnishes, and adhesives.
Acetone effectively dissolves and removes various substances, making it a valuable cleaning agent and solvent for surface preparation.

Nail polish remover:
Acetone is a common ingredient in nail polish removers.
Its solvent properties help dissolve and remove nail polish quickly and efficiently.

Pharmaceuticals:
Acetone is used in the pharmaceutical industry as a solvent for various active ingredients and excipients during the formulation of medications.

Chemical synthesis:
Acetone serves as a reactant and solvent in the synthesis of numerous chemicals and organic compounds.
Acetone is a key component in the production of methyl methacrylate, bisphenol-A, methyl isobutyl ketone (MIBK), and other important chemicals.

Cleaning and degreasing:
Acetone's excellent solvent properties make it effective for cleaning and degreasing surfaces, machinery, and equipment in industrial settings.
Acetone is commonly used to remove oils, greases, and residues from metal parts.

Paint and coating industry:
Acetone is utilized in the formulation of paints, varnishes, and lacquers.
Acetone helps dissolve and disperse pigments and resins, aiding in the production of high-quality coatings.

Printing industry:
Acetone is used in the production of printing inks.
Acetone helps dissolve the ink components and facilitates smooth and consistent printing.

Extraction of natural products:
Acetone is employed in the extraction of natural products, such as essential oils from plants.
Acetone acts as a solvent, enabling the separation and concentration of the desired compounds.

Personal care products:
Acetone is used in the formulation of various personal care products, including perfumes, lotions, and cosmetics.
Acetone can act as a solvent for fragrance oils and other ingredients.

Laboratory and research:
Acetone finds applications in laboratories for various analytical and research purposes.
Acetone is used as a solvent for chemical reactions, sample preparation, and cleaning laboratory equipment.

Fuel additive:
Acetone can be used as a fuel additive, primarily in engines that use gasoline or diesel.
Acetone is believed to improve combustion efficiency and reduce fuel consumption.

Fiber and textile industry:
Acetone is utilized in the production of synthetic fibers like rayon and acetate.
Acetone helps dissolve and spin the polymer solutions into fibers.

Rubber industry:
Acetone is involved in the production and processing of rubber.
Acetone aids in the extraction of rubber from latex and acts as a solvent for various rubber-related processes.

Adhesives and sealants:
Acetone is a common component in the formulation of adhesives and sealants.
Acetone helps dissolve and disperse adhesive ingredients, enabling effective bonding and sealing.

Electronics industry:
Acetone is used in the electronics industry for cleaning and degreasing electronic components and printed circuit boards.
Acetone helps remove solder flux, oils, and other contaminants.

Automotive industry:
Acetone finds applications in the automotive industry for cleaning and degreasing auto parts, engines, and machinery.
Acetone helps remove dirt, grime, and oil residues.

Analytical chemistry:
Acetone is employed as a common solvent in analytical chemistry techniques such as chromatography and spectrophotometry.
Acetone aids in sample preparation and analysis.

Cosmetics and skincare:
Acetone is used in the formulation of cosmetics and skincare products, such as toners and astringents.
Acetone can help remove excess oil and clean the skin.

Printing and photography:
Acetone is used in the printing and photography industry for cleaning printing plates and removing inks.
Acetone helps dissolve and remove ink residues.

Agrochemicals:
Acetone is involved in the production of certain agrochemicals, including pesticides and herbicides.
Acetone serves as a solvent and a reactant in the synthesis of these compounds.

Surface coatings and laminates:
Acetone is used in the production of surface coatings and laminates, including automotive paints, furniture finishes, and protective coatings.

Metalworking industry:
Acetone finds applications in metalworking for cleaning and degreasing metal surfaces before coating or processing.
Acetone helps remove oils, greases, and residues that could affect the quality of the finished products.



DESCRIPTION


Acetone is a colorless, volatile, and flammable organic compound with the chemical formula C3H6O.
Acetone is the simplest and smallest ketone, consisting of a carbonyl group (C=O) bonded to two methyl groups (-CH3).
Acetone is highly miscible with water, alcohol, and other organic solvents, making it a versatile solvent widely used in various industries and everyday applications.

Acetone is produced naturally in small quantities in the human body through metabolic processes, but it is primarily manufactured industrially.
Acetone is commonly obtained as a byproduct during the production of phenol, where it is derived from cumene.

Acetone can also be synthesized via the oxidation of isopropanol.
Acetone has a distinct fruity or sweet odor and a low boiling point, which contributes to its rapid evaporation.

Acetone is highly volatile and highly flammable, so it should be handled with care and stored properly.
Due to its excellent solvent properties, acetone finds applications in many industries.

Acetone is widely used as a solvent for paints, varnishes, resins, and coatings.
Acetone is also used as a cleaning agent for removing oils, greases, and other contaminants from surfaces.
Additionally, acetone is utilized as a solvent in the production of pharmaceuticals, cosmetics, and personal care products.

Moreover, acetone is a key ingredient in many chemical reactions and processes.
Acetone is used as a reactant in the production of various chemicals, including methyl methacrylate, bisphenol-A, and methyl isobutyl ketone (MIBK).
Acetone is also utilized as a denaturant in alcohol products and as a fuel additive in some engines.

Acetone is a colorless liquid with a distinct fruity odor.
Acetone has a boiling point of approximately 56 degrees Celsius.

Acetone is highly flammable and should be stored away from open flames or ignition sources.
Acetone is soluble in water, alcohol, and many organic solvents.
Acetone has a rapid evaporation rate due to its low boiling point.

Acetone is a common ingredient in nail polish removers.
Acetone is widely used as a solvent for paints, varnishes, and lacquers.

Acetone is a key component in the production of plastics, fibers, and synthetic resins.
Acetone has a wide range of industrial applications, including cleaning agents and degreasers.

Acetone is used in laboratories for various analytical and research purposes.
Acetone is a volatile organic compound (VOC) and contributes to air pollution when released into the atmosphere.
Acetone has a relatively low toxicity level but can cause irritation to the skin, eyes, and respiratory system.

Acetone is commonly used as a cleaning agent for removing adhesive residues.
Acetone is a vital component in the production of methyl methacrylate, a key ingredient in acrylic plastics.

Acetone is utilized in the synthesis of pharmaceuticals and organic compounds.
Acetone is an important ingredient in the manufacturing of printing inks.

Acetone can be used as a fuel additive to improve combustion efficiency.
Acetone is a volatile solvent commonly used for dissolving and removing grease and oil stains.
Acetone is used as a cleaning solvent for electronic components and circuit boards.

Acetone has a characteristic sweet taste but should never be ingested as it is toxic in large quantities.
Acetone can act as a drying agent, helping to speed up the drying process of certain materials.

Acetone is used in the extraction of natural products, such as essential oils.
Acetone is used in the production of artificial fibers like rayon and acetate.

Acetone is an essential component in the formulation of many personal care products, including perfumes and cosmetics.
Acetone is a versatile chemical compound with numerous industrial, commercial, and household applications.



PROPERTIES


Chemical formula: C3H6O
Molecular weight: 58.08 g/mol
Appearance: Clear, colorless liquid
Odor: Sweet, fruity odor
Melting point: -94.9°C (-138.8°F)
Boiling point: 56.1°C (132.9°F)
Density: 0.79 g/cm³
Solubility: Highly soluble in water, miscible with many organic solvents
Vapor pressure: 227 mmHg at 20°C
Vapor density: 2.0 (air = 1)
Flash point: -17.8°C (0°F)
Autoignition temperature: 465°C (869°F)
Refractive index: 1.358
Heat of vaporization: 31.3 kJ/mol
Flammability: Highly flammable liquid
Explosive limits: 2.6% to 13.0% (volume percent in air)
pH: Neutral (approximately 7)
Miscibility: Miscible with water, ethanol, methanol, ether, chloroform, and many organic solvents
Volatility: High volatility, evaporates quickly
Stability: Stable under normal conditions, but can form explosive mixtures with air



FIRST AID


Inhalation:

If inhaled, remove the affected person from the contaminated area to fresh air.
If the person is experiencing difficulty breathing, provide oxygen if available and seek immediate medical attention.
If the person is not breathing, perform artificial respiration and seek immediate medical attention.


Skin Contact:

Remove contaminated clothing and immediately wash the affected area with plenty of soap and water for at least 15 minutes.
If irritation or redness persists, seek medical attention.
Do not use solvents or harsh chemicals to remove acetone from the skin.


Eye Contact:

Rinse the eyes thoroughly with gently flowing water for at least 15 minutes, while holding the eyelids open.
Remove contact lenses if present and easy to do.
Seek immediate medical attention, even if the person feels no discomfort.


Ingestion:

Do not induce vomiting unless instructed to do so by medical professionals.
Rinse the mouth with water and drink plenty of water, if the person is conscious and able to swallow.
Seek immediate medical attention or contact a poison control center.


General First Aid:

If any symptoms develop or persist, seek medical attention promptly.
Provide medical personnel with all relevant information, including the quantity and route of exposure.
It is important to note that acetone is a flammable substance, so keep away from open flames or ignition sources.



HANDLING AND STORAGE


Handling:

Use appropriate personal protective equipment (PPE) when handling acetone, including gloves, safety goggles, and a lab coat or protective clothing.
Ensure good ventilation in the working area to minimize the buildup of vapors. Use local exhaust ventilation if necessary.

Keep acetone away from open flames, sparks, or any potential sources of ignition, as it is highly flammable.
Avoid contact with skin, eyes, and clothing. In case of contact, promptly remove contaminated clothing and wash the affected area thoroughly with soap and water.
Do not eat, drink, or smoke while working with acetone.

Use suitable chemical-resistant containers and equipment for storage and handling.
Avoid breathing in vapors or mists. If working with acetone in an enclosed area, use appropriate respiratory protection.
Do not use acetone near electrical equipment or in areas where static sparks may occur.


Storage:

Store acetone in a cool, well-ventilated area, away from direct sunlight and heat sources.
Keep acetone containers tightly closed when not in use to prevent evaporation and minimize the risk of fire.
Store acetone separately from oxidizing agents, acids, and alkalis to avoid potential chemical reactions.

Use appropriate secondary containment measures, such as spill trays or cabinets, to prevent leakage or spills.
Clearly label storage containers with the name of the substance and appropriate hazard warnings.
Store acetone away from incompatible materials, such as strong oxidizers, strong acids, and bases.

Ensure proper grounding and bonding during transfer operations to minimize the risk of static discharge.
Keep storage areas secure and restrict access to authorized personnel only.
Regularly inspect storage areas for leaks, spills, or signs of damage. Clean up any spills promptly using appropriate absorbent materials and dispose of them safely.



SYNONYMS


Propanone
Dimethyl ketone
2-Propanone
Dimethylformaldehyde
Methyl ketone
β-Ketopropane
Pyroacetic spirit
Ketone propane
Ketone dimethyl
Pyroacetic ether
Ketopropane
Propan-2-one
Beta-ketopropane
Methyl propanone
Propan-2-one
2-Oxopropane
2-Ketopropane
Dimethyl formaldehyde
Dimethyl ketone
Dimethylformaldehyde
Dimethylformaldehyde
Ethanone
Methyl acetone
Methyl ethyl ketone
Methylketone
Propanone, dimethyl
Propanone, 2-methyl-
Propanone, 2-propyl-
Pyroacetic ether
Pyroacetic spirit
Pyroacetic alcohol
Pyroacetic acid
Pyroacetic acid ether
Pyroacetic acid methyl ester
Pyroacetic acid, ethyl ester
Pyroacetic acid, methyl ester
2-Propanone, 1,1-dimethyl-
Ketone propane
Ketone dimethyl
Propanone, 1,1-dimethyl-
Propanone, methyl-
Propione
Dimethylformaldehyde
Dimethylketone
Dimethylformaldehyde
2-Oxopropane
Propanone, dimethyl-
Propanone, 2-methyl-
Propanone, 2-propyl-
Propanone, 2-methyl-
Ethyl methyl ketone
Methyl acetone
Methyl ethyl ketone
Methylpropane-2-one
Beta-ketopropane
2-Ketopropane
Pyroacetic acid
Pyroacetic acid ether
Pyroacetic alcohol
Pyroacetic acid methyl ester
Pyroacetic acid, ethyl ester
Pyroacetic acid, methyl ester
ACETONE
Acetone = dimethyl ketone

CAS NUMBER: 67-64-1
MOLECULAR FORMULA: C3H6O

Acetone, or propanone, is an organic compound with the formula (CH3)2CO.
Acetone is the simplest and smallest ketone.
Acetone is a colourless, highly volatile and flammable liquid with a characteristic pungent odour.
Acetone is miscible with water and serves as an important organic solvent in Acetones own right, in industry, home, and laboratory.

Acetone is a naturally occurring compound also known as propanone.
Composed of the elements carbon, hydrogen, and oxygen, acetone presents as a clear liquid that is highly flammable and often used as cleaner in industrial settings.
Acetone is found in volcanic gases, plants, in byproducts of forest fires, and the breakdown of body fat.
Acetone evaporates very quickly, and while Acetone is produced in nature, for commercial use Acetone is produced by manually combining three carbon atoms, six hydrogen atoms, and one oxygen atom to produce the compound element (CH3)2CO, that we call acetone.
Because acetone is both organic and non-toxic, when used properly, Acetone is an element many products that people use every day.

Acetone is the main ingredient in paint thinner, used as a solvent in various cosmetics and facial treatments, as well as a cleaning agent to remove sticky substances like glue or resin.
Acetone is also used as an additive in gasoline that thins the gas allowing Acetone to diffuse more easily through the engine, resulting in higher fuel efficiency.
Acetone is a chemical that is used daily by many people.
Across all industries acetone is necessary for developing new products, cleaning, degreasing, or even saving marine life from detrimental oil spills.

USES:
Acetone is a good solvent for many plastics and some synthetic fibers.
Acetone is used for thinning polyester resin, cleaning tools used with Acetone, and dissolving two-part epoxies and superglue before they harden.
Acetone is used as one of the volatile components of some paints and varnishes.
As a heavy-duty degreaser, Acetone is useful in the preparation of metal prior to painting or soldering, and to remove rosin flux after soldering (to prevent adhesion of dirt and electrical leakage and perhaps corrosion or for cosmetic reasons), although Acetone attacks many electronic components (for example polystyrene capacitors) so Acetone is unsuitable for cleaning many circuit boards.
Although itself flammable, acetone is used extensively as a solvent for the safe transportation and storage of acetylene, which cannot be safely pressurized as a pure compound.

Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone.
One litre of acetone can dissolve around 250 litres of acetylene at a pressure of 10 bars (1.0 MPa).
Acetone is a primary ingredient in many nail polish removers.
Acetone breaks down nail polish, making Acetone easy to remove with a cotton swab or cloth.
Acetone is widely used because Acetone can easily mix with water and evaporates quickly in the air.

Acetone is widely used in the textile industry for degreasing wool and degumming silk.
As a solvent, acetone is frequently incorporated in solvent systems or “blends,” used in the formulation of lacquers for automotive and furniture finishes.
Acetone also may be used to reduce the viscosity of lacquer solutions.
Acetone is commonly used as a solvent to manufacture plastics and other industrial products.

Acetone may also be used to a limited extent in household products, including cosmetics and personal care products, where its most frequent application would be in the formulation of nail polish removers.
Acetone is used as a solvent in the cosmetics industry (nail polish remover).
Acetone is used as a thinner and solvent in the paint industry.

About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and production of methyl methacrylate and bisphenol A.
Acetone is a common building block in organic chemistry.
Familiar household uses of acetone are as the active ingredient in nail polish remover and as paint thinner.
While Acetone has volatile organic compound (VOC) exempt status in the United States, Acetone is considered by the EU as a contributor to environmental pollution.

Acetone is used in the preparation of paper coatings, adhesives, and heat-seal coatings and is also employed as a starting material in the synthesis of many compounds.
The cumene hydroperoxide process is the dominant process used in the commercial production of acetone.
Acetone is also prepared by the dehydrogenation of 2-propanol (isopropyl alcohol).
The first member of the ketones class is dimethyl ketone.
Acetones closed formula is C3H6O, Acetones boiling point is 56 °C.
Acetone combines with water, ethanol and ether at any rate.

Acetone smells sharp. From the dry-dry distillation of wood: from heating calcium acetate; dehydrogenation of isopropanol from copper catalysts in the art at 250 °C; Acetone is obtained from the mixture of ethanol and water vapor in the gas phase at 250 °C under the catalysis of Fe2O3.
If acetone and sodium nitrozil prussiat are mixed in basic medium, red precipitation occurs, acetone is detected.
An important reaction is the formation of iodoform, which Acetone gives with elemental iodine in a basic environment.
Acetone is in the cigarette.
Acetone is a polar organic solvent.
Acetone can undergo photocatalytic oxidation in the presence of mixed TiO2-rare earth oxides.

Acetone is produced and disposed of in the human body through normal metabolic processes.
Acetone is normally present in blood and urine. People with diabetic ketoacidosis produce Acetone in larger amounts. Reproductive toxicity tests show that Acetone has low potential to cause reproductive problems.
Ketogenic diets that increase ketone bodies (acetone, β-hydroxybutyric acid and acetoacetic acid) in the blood are used to counter epileptic attacks in infants and children who suffer from refractory epilepsy.
Acetone is a colorless, volatile, flammable organic solvent.
Acetone occurs naturally in plants, trees, forest fires, vehicle exhaust and as a breakdown product of animal fat metabolism.
This agent may be normally present in very small quantities in urine and blood; larger amounts may be found in the urine and blood of diabetics.
Acetone is toxic in high doses.

Acetone is a manufactured chemical that is also found naturally in the environment.
Acetone is a colorless liquid with a distinct smell and taste.
Acetone evaporates easily, is flammable, and dissolves in water.
Acetone is also called dimethyl ketone, 2-propanone, and beta-ketopropane.
Acetone is used to make plastic, fibers, drugs, and other chemicals.
Acetone is also used to dissolve other substances.

Acetone occurs naturally in plants, trees, volcanic gases, forest fires, and as a product of the breakdown of body fat.
Acetone is present in vehicle exhaust, tobacco smoke, and landfill sites.
Industrial processes contribute more acetone to the environment than natural processes.
Acetone appears as a clear colorless liquid with a sweetish odor.
Flash point 0°F. Less dense than water.
Vapors are heavier than air.
Used as a solvent in paint and nail polish removers.

Acetone, a colorless liquid also known as Propanone, is a solvent used in manufacture of plastics and other industrial products.
Acetone may also be used to a limited extent in household products, including cosmetics and personal care products, where Acetones most frequent application would be in the formulation of nail polish removers.
Acetone occurs naturally in the human body as a byproduct of metabolism.
Acetone occurs naturally in the human body as a byproduct of metabolism.
Acetone is also a primary ingredient in many nail polish removers.

As a solvent, acetone is frequently incorporated in other solvent systems or “blends,” used in the formulation of lacquers for automotive and furniture finishes, for example.
In chemistry, a pure chemical compound is a chemical substance which contains only one substance and a particular set of molecules or ions.
Pure acetone contains only the molecules or ions of acetone.
Acetone is a chemical used to make products like nail polish remover and paint remover.
Your body also makes this chemical when Acetone breaks down fat.

Acetone is safe in normal amounts, but too much of Acetone could be a problem.
Acetone is a solvent, which means Acetone can break down or dissolve substances like paint and varnish.
That's why it's an ingredient in nail polish removers, varnish removers, and paint removers. Companies also use this chemical to remove grease from wool, reduce the stickiness of silk, and make protective coatings for furniture and cars.
Acetone (CH3COCH3), also called 2-propanone or dimethyl ketone, organic solvent of industrial and chemical significance, the simplest and most important of the aliphatic (fat-derived) ketones.

Pure acetone is a colourless, somewhat aromatic, flammable, mobile liquid that boils at 56.2 °C (133 °F).
Acetone is capable of dissolving many fats and resins as well as cellulose ethers, cellulose acetate, nitrocellulose, and other cellulose esters.
Because of the latter quality, acetone is used extensively in the manufacture of artificial fibres (such as some rayons) and explosives.
Acetone is used as a chemical intermediate in pharmaceuticals and as a solvent for vinyl and acrylic resins, lacquers, alkyd paints, inks, cosmetics (such as nail-polish remover), and varnishes.

Acetone is a volatile, flammable liquid.
Acetone is rapidly absorbed by inhalation, ingestion, and dermally, and distributed throughout the body.
Once acetone has been absorbed, Acetone is metabolized, but the pharmacokinetics and the selection of metabolic pathway seem to be dose dependent.
Excretion of acetone appears in breath and urine.

Inhaled acetone is narcotic and causes transient central nervous system effects, but Acetone is not a neurotoxicant.
In occupational environments, workers exposed to acetone for weeks do not exhibit long-lasting complaints.
Acetone is neither genotoxic nor mutagenic.
As Acetone now looks, acetone is hazardous because of Acetones potentiating effect on the toxicity of other volatile organic solvents and methylglyoxal.
Acetone, also known as 2-propanone or dimethyl ketone (DMK), is an important chemical intermediate used in the production of acrylic plastics, polycarbonates and epoxy resins.

These materials in turn are used by many different industry sectors to product countless everyday items.
Acetone is also used in its own right as a solvent.
Acetone is manufactured from the basic raw materials of benzene and propylene.
These materials are first used to produce cumene, which is then oxidised to become cumene hydroperoxide, before being split into phenol and its co-product, acetone.
Acetone is the simplest example of the ketones.
Acetone is a clear, colorless, mobile liquid.

Acetone is completely miscible with water and most organic solvents and oils.
Acetone therefore serves as an important industrial solvent for cleaning, as a common building block in organic chemistry, and as a precursor to polymers.
Well-known domestic uses of acetone are as the active ingredient in nail polish remover and as paint thinner.
Acetone is a normal by-product of mammalian metabolism and is thus found in all tissues, including blood, as well as in urine and breath.
The levels vary, depending on nutritional and metabolic conditions, and are increased in obese compared with slim people and in working compared with resting people.

Diabetic patients show markedly elevated levels of acetone.
Acetone is an organic element with formula (CH3)2CO.
Acetone consists of three carbon, six hydrogens and one oxygen atom.
Acetone comes under the categories of ketones, which are organic compounds with a carbonyl group bonded to two hydrocarbon groups.
Acetone is a general building block in organic chemistry.

In the human body, Acetone is normally present in blood and urine.
Acetone is readily taken up via inhalation if present in ambient air and via the gastrointestinal tract if ingested.
Uptake via skin is of minor importance.
However, due to its excellent solvent properties, acetone readily removes water from the skin.
This impairs the barrier properties and makes the skin more vulnerable to other irritating, sensitizing, or infectious agents.

Acetone evaporates easily, meaning that Acetone changes into a vapor.
Acetone catches fire easily and burns rapidly. Acetone will dissolve in water.
Acetone also has a wide variety of applications from solvents to chemical intermediates and is used in the production of acrylics, polycarbonates and fine chemical intermediates.

Acetone is a clear liquid that smells like nail polish remover.
When exposed to the air, Acetone quickly evaporates and remains highly flammable.
Acetone is dangerous to use around an open flame.
Hundreds of commonly used household products contain acetone, including furniture polish, rubbing alcohol, and nail polish.

Acetone is one of the most widely used industrial solvents.
Acetone is used in surface coatings, cleaning fluids, pharmaceutical applications, adhesives and numerous other consumer and commercial products.
Commercial products that may contain acetone include cleaners for automotive engines and automotive parts, wood cleaners, floor wax and paint thinners.
Acetone is widely used as a chemical intermediate in the production of other chemicals and solvents.

Acetone is often used in captive processes for preparing downstream chemicals.
Acetone is also used as a formulating solvent for commercial products.
Acetone (also known as propanone, dimethyl ketone, 2-propanone, propan-2-one and β-ketopropane) is the simplest representative of the group of chemical compounds known as ketones.

Acetone is a colorless, volatile, flammable liquid.
Acetone is miscible with water and serves as an important laboratory solvent for cleaning purposes.
Acetone is a highly effective solvent for many organic compounds such as Methanol, ethanol, ether, chloroform, pyridine, etc., and is the active ingredient in nail polish remover.
Acetone is also used to make various plastics, fibers, drugs, and other chemicals.

Acetone exists in nature in the Free State.
In the plants, it mainly exists in essential oils, such as tea oil, rosin essential oil, citrus oil, etc.; human urine and blood and animal urine, marine animal tissue and body fluids contain a small amount of acetone.
Acetone is a flammable, colorless liquid with a pleasant odor.
Acetone is used widely as an organic solvent and in the chemical industry.
Acetone is the simplest ketone, which also goes by the name dimethyl ketone (DMK).
Acetone was originally referred to as pyroacetic spirit because Acetone was obtained from the destructive distillation of acetates and acetic acid.

Acetone is used in industry for the production of most chemicals.
Almost half of the world production of acetone is used as a precursor in the production of methylmetacrylate.
Acetones second main use in industry is Acetones use in the production of bisphenol A, which is bisphenol A; Polycarbonate is the main component of most polymers such as polyurethane and epoxy resins.
Acetone is used in the production of cleaning materials.
Acetone is a very good glass cleaner.
Acetone is used as a common solvent in the pharmaceutical industry.
Acetone also reacts as an excipient in most various drugs.
While Acetone appears as a component in the packaging section in the food sector, Acetone is also used as additives in this sector.

Acetone is the most widely used chemical in nail polish cleaning in this sector.
They are preferred for cleaning glass laboratory materials, which are the most common and common areas of use in the chemical industry, and to provide high efficiency drying in a short time.
In addition, Acetone interacts with substances such as salicylic acid and glycolic acid, which is called peeling (chemical peeling), and creates an auxiliary factor in this method.
The evaporation rate of acetone from water and soil is quite high.
Acetone is an important underground pollutant for soil due to Acetones high solubility in water consumed by animals or sometimes microorganisms.

For fish, acetone is a very harmful substance with its LD50 value of 8.3 g / L and its half-life.
Oxygen depletion can pose a significant risk in systems with high acetone-consuming microbial activity.
Most acetone is consumed as an intermediate feedstock for acrylic plastics used for glazing, signs, lighting fixtures and displays, and for production of Bisphenol A (BPA) which, in turn, is used to manufacture polycarbonate and epoxy resins.
Both polycarbonate and epoxy resins are used in many different industries and in countless items which we encounter every day.

Acetone is also used extensively in the manufacture of artificial fibres and as an intermediate in pharmaceuticals.
Acetone is one of the most widely used solvents in the world due to is combination of high solvency and a high rate of evaporation.
Acetone can be found in many everyday products including paints, cleaning fluids, nail polish remover, and adhesives.
Acetone is a colourless, low boiling, easy pouring liquid with a characteristic odour.

Acetone is miscible in all proportions with water, alcohols, many hydrocarbons and other organic liquids.
Acetone has good solvent properties for vegetable and animal fats, cellulose, natural and synthetic resins and many other organic substances.
Acetone's listing as a non-volatile organic compound (VOC) in the US is increasing Acetones use in coatings applications.
Acetone is a colorless solvent. Solvents are substances that can break down or dissolve other materials.
In the household, people may come across acetone in products such as nail polish remover or paint remover.

Acetone occurs naturally in the environment in trees, plants, volcanic gases, and forest fires.
Small amounts are also present in the body.
But exposure to acetone can irritate the eyes, nose, or skin.
Consuming Acetone can lead to acetone poisoning.
Acetone is a clear, colorless liquid.

Acetone is a solvent that can dissolve or break down other materials, such as paint, varnish, or grease.
Acetone evaporates quickly into the air.
Acetone is naturally present in trees and other plants, as well as tobacco smoke, vehicle exhaust, and landfills.
Acetone also occurs in the body.

Acetone is the most widely used ketone in industry.
Acetone is used primarily to synthesize methacrylates, about half of the world's production of acetone is used as a precursor to methyl methacrylate.
Other large-scale chemicals derived from acetone are bisphenol A and methyl isobutyl ketone.
Acetone is also used as a process solvent in the manufacture of cellulose acetate yarn, smokeless gun powder, surface coatings, and various pharmaceutical and cosmetic products.

Other solvent uses include paint, ink, resin, and varnish formulations; thinning of fiberglass resin; cleaning of fiberglass tools; and dissolution of two-part epoxies and superglues before hardening.
Acetone is found in nature in plants, trees, gas from volcanoes, and forest fires.
Also, when your body breaks down fat, it produces acetone.
If you are on a low fat diet, you will have more acetone in your body.

Acetone is found in exhaust from cars and trucks, tobacco smoke and landfills.
Factories release acetone into the air.
Acetone is used to make plastic, fibers, drugs and chemicals.
Acetone is often used as a solvent.
Solvents help other substances dissolve.

Acetone is used in the chemical industry in numerous applications.
The primary use of acetone is to produce acetone cyanohydrin, which is then used in the production of methyl methacrylate (MMA).
Another use of acetone in the chemical industry is for bisphenol A (BPA).
BPA results form the condensation reaction of acetone and phenol in the presence of an appropriate catalyst.
BPA is used in polycarbonate plastics, polyurethanes, and epoxy resins. Polycarbonate plastics are tough and durable and are often used as a glass substitute.
In addition to its use as a chemical feedstock and intermediate, acetone is used extensively as an organic solvent in lacquers, varnishes, pharmaceuticals, and cosmetics.
Nail polish remover is one of the most common products containing acetone.

Acetone is used to stabilize acetylene for transport .
Acetone is used in the manufacture of a largenumber of compounds, such as acetic acid,chloroform, mesityl oxide, and MIBK; in themanufacture of rayon, photographic films,and explosives; as a common solvent; inpaint and varnish removers; and for purifyingparaffins.
Solvent for fats, oils, waxes, resins, rubber, plastics, lacquers, varnishes, rubber cements. manufacture of methyl isobutyl ketone, mesityl oxide, acetic acid (ketene process), diacetone alcohol, chloroform, iodoform, bromoform, explosives, aeroplane dopes, rayon, photographic films, isoprene; storing acetylene gas (takes up about 24 times its vol of the gas); extraction of various principles from animal and plant substances; in paint and varnish removers; purifying paraffin; hardening and dehydrating tissues.
Pharmaceutic aid (solvent). acetone is a solvent considered to be non-comedogenic and occasionally used in skin toners.
Acetone is primarily used in nail polish remover.
Acetone could be drying and very irritating to the skin depending on the concentration and frequency of use.

Companies use acetone in small amounts to create products that break down or dissolve other substances, such as:
-nail polish
-paint
-varnish

In industry, manufacturers use acetone for a variety of purposes, including:
-removing grease or gum from textiles such as wool and silk
-making lacquers for cars or furniture
-making plastics

According to Addiction Resource, some people also consume or inhale acetone-based nail polish remover in order to achieve a “high”.
This is because nail polish remover can also contain alcohol.
Doing this is very dangerous, as the chemicals in nail polish remover can seriously damage the kidneys, liver, brain, and nervous system.
About a third of the world's acetone is used as a solvent, and a quarter is consumed as acetone cyanohydrin, a precursor to methyl methacrylate.

USES:
-An important organic raw material in the chemical, artificial fiber, medicine, paint, plastics, organic glass, cosmetics and other industries; an excellent organic solvent that dissolves many organic products such as resin, cellulose acetate, acetylene and so on.
-An important raw material for the synthesis of ketene, acetic anhydride, iodoform, polyisoprene rubber, methacrylic acid, methyl ester, chloroform, and epoxy resins.
-The acetone cyanohydrin obtained from the reaction of acetone with hydrocyanic acid is the raw material of methacrylic resin (perspex).
-A raw material in the production of epoxy resin intermediate bisphenol A.
-In pharmaceuticals, acetone is used as extractants for a variety of vitamins and hormones in addition to vitamin C, and dewaxing solvents for petroleum refining.
-A raw material for nail polish remover in cosmetics
-One of the raw materials for synthesizing pyrethroids in pesticide industry
-Acetone is often used to wipe the black ink above the copper tube in the precision copper tube industry.

INDUSTRIAL USES:
Acetone is valuable solvent component in acrylic/nitrocellulose automotive lacquers.
Acetone is the solvent of choice in film coatings operations which use vinylidene chloride-acrylonitrile copolymer formulations.
Other ketones that may be used in these film coating operations include methyl isobutyl ketone, ethyl n-amyl ketone, and diisobutyl ketone.
Acetone, blends of MIBK and MEK, methyl namyl ketone, ethyl n-amyl ketone, and diisobutyl ketone are all useful solvents for vinyl resin copolymers.
The presence of one of the slower evaporating ketones in the solvent blend prevents quick drying, improves flow, and gives blush resistance to the coating.

Acetone is also used as a resin thinner in polyester resins and as a clean up solvent for the resin reactor kettle.
In solvents industry, Acetone is a component of solvent blends in urethane, nitrile rubber, and neoprene industrial adhesives.
Acetone is the primary solvent in resin-type adhesives and pressure sensitive chlorinated rubber adhesives.
Acetone also can be used to extract fats, oils, waxes, and resins from natural products, to dewax lubricating oils, and to extract certain essential oils.
Acetone is also an important chemical intermediate in the preparation of several oxygenated solvents including the ketones, diacetone alcohol, mesityl oxide, methyl isobutyl ketone, and isophorone.

HIGHLIGHTS:
-Acetone polish remover helps you get a fresh start for a new coat
-Free from phthalate, parabens, aluminum, and dye for safe use
-Made with acetone to help remove artificial nails, gel polish and
-If you’re not satisfied with any Target Owned Brand item, return it within one year with a receipt for an exchange or a refund

APPLICATION:
Acetone′s luminesence intensity is dependent upon the solution components.
The absorption of UV light by acetone, results in its photolysis and the production of radials .
Acetone may be used in the synthesis of Ga (Gallium)-DOTATATE (where DOTA= 1,4,7,10-tetraazacyclo- dodecane -1,4,7,10-tetraacetic acid) chemicals.
Acetone may be used in an assay for the determination of ester groups in lipids by spectrophotometric methods.
Acetone undergoes aldolization in the presence of Mg-Al layered double hydroxides (LDH) as catalysts and Cl- and/or CO32- as compensating anions to afford diacetone alcohol and mesityl oxide as the main products.
Acetones enantioselective Aldol condensation with various isatins in the presence of a dipeptide catalyst forms 1-alkyl 3-(2-oxopropyl)-3-hydroxyindolin-2-ones.
Aqueous solution of acetone may be used as a medium for the oxidation of alkynes to 1,2-diketones using potassium permanganate.

PHARMACEUTICAL APPLICATION:
Acetone is used as a solvent or cosolvent in topical preparations, and as an aid in wet granulation.
Acetone has also been used when formulating tablets with water-sensitive active ingredients, or to solvate poorly water-soluble binders in a wet granulation process.
Acetone has also been used in the formulation of microspheres to enhance drug release.
Owing to its low boiling point, acetone has been used to extract thermolabile substances from crude drugs.

PHYSICAL AND CHEMICAL PROPERTIES:
-Appearance Form: liquid
-Color: colorless
-Odor: pungent, weakly aromatic
-Odor: Threshold 0,1 ppm
-pH: 5 - 6 at 395 g/l at 20 °C
-Melting point/freezing point: Melting point/range: -94,0 °C
-Initial boiling point and boiling range: 56,0 °C at 1.013 hPa
-Flash point: -17,0 °C - closed cup
-Upper/lower flammability or explosive limits: Upper explosion limit: 13 %(V) Lower explosion limit: 2 %(V)
-Vapor pressure: 245,3 hPa at 20,0 °C
-Density: 0,79 g/cm3 at 20 °C
-Water solubility: soluble, in all proportions
-Autoignition temperature: 465,0 °C
-Decomposition temperature: Distillable in an undecomposed state at normal pressure.

HOW DOES ACETONE WORK:
Acetone enters the body through the lungs, mouth or the skin.
Acetone can also be in the body from the breakdown of fat.
Your blood carries acetone to all your body organs.
Small amounts of acetone in your body usually will
not hurt you because your liver breaks the acetone down into other harmless chemicals.

HANDLING:
Eliminate heat and ignition sources such as sparks, open flames, hot surfaces and static discharge.
Post "No Smoking" signs.
Electrically bond and ground equipment. Ground clips must contact bare metal.
Do not weld, cut or perform hot work on empty container until all traces of product have been removed.

STORAGE:
Store in an area that is: cool, well-ventilated, out of direct sunlight and away from heat and ignition sources.
Electrically bond and ground containers.
Ground clips must contact bare metal.
Install pressure and vacuum-relief venting in all drums.
Equip storage tank vents with a flame arrestor.

CHEMICAL PROPERTIES

-Keto/enol tautomerism:
Like most ketones, acetone exhibits the keto–enol tautomerism in which the nominal keto structure (CH3) 2C=O of acetone itself is in equilibrium with the enol isomer (CH3)C(OH)=(CH2) (prop-1-en-2-ol).
In acetone vapor at ambient temperature, only 2.4×10−7% of the molecules are in the enol form.
Yet the enol form is chemically important in some chemical reactions.

-Aldol condensation:

In the presence of suitable catalysts, two acetone molecules also combine to form the compound diacetone alcohol (CH3)C=O(CH2)C(OH)(CH3)2, which on dehydration gives mesityl oxide (CH3)C=O(CH)=C(CH3)
This product can further combine with another acetone molecule, with loss of another molecule of water, yielding phorone and other compounds.

-Polymerisation:
One might expect acetone to also form polymers and (possibly cyclic) oligomers of two types.
In one type, units could be acetone molecules linked by ether bridges –O– derived by from the opening of the double bond, to give a polyketal-like (PKA) chain [–O–C(CH3)2–]n.
The other type could be obtained through repeated aldol condensation, with one molecule of water removed at each step, yielding a poly(methylacetylene) (PMA) chain [–CH=C(CH3)–]n.

-PKA type:
The conversion of acetone to a polyketal (PKA) would be analogous to the formation of paraformaldehyde from formol, and of trithioacetone from thioacetone.
In 1960, Kargin, Kabanov and others observed that the thermodynamics of this process is unfavourable for liquid acetone, so that it (unlike thioacetone and formol) is not expected to polymerise spontaneously, even with catalysts.
However, they observed that the thermodynamics became favourable for crystalline solid acetone at the melting point (−96 °C).
They claimed to have obtained such a polymer (a white elastic solid, soluble in acetone, stable for several hours at room temperature) by depositing vapor of acetone, with some magnesium as a catalyst, onto a very cold surface.
In 1962, Wasaburo Kawai reported the synthesis of a similar product, from liquid acetone cooled to −70 to −78 °C, using n-butyl lithium or triethylaluminium as catalysts.
He claimed that the infrared absorption spectrum showed the presence of –O– linkages but no C=O groups.
However, conflicting results were obtained later by other investigators.

-PMA type:
The PMA type polymers of acetone would be equivalent to the product of polymerisation of propyne, except for a keto end group.

PRODUCTION:
In 2010, the worldwide production capacity for acetone was estimated at 6.7 million tonnes per year.
With 1.56 million tonnes per year, the United States had the highest production capacity, followed by Taiwan and mainland China.
The largest producer of acetone is INEOS Phenol, owning 17% of the world's capacity, with also significant capacity (7–8%) by Mitsui, Sunoco and Shell in 2010.
INEOS Phenol also owns the world's largest production site (420,000 tonnes/annum) in Beveren (Belgium).
Spot price of acetone in summer 2011 was 1100–1250 USD/tonne in the United States.

ACETONE IN BODY:
In humans, acetone is a natural byproduct of the breakdown of fat.
The body can make energy in several ways.
The first is by turning food substances such as carbohydrates into glucose.
The body then releases insulin, which allows the body’s cells to use glucose for energy or store some of the glucose in fat, the liver, and muscles.

But if a person is not eating many carbohydrates, the body cannot use dietary glucose for energy.
Instead, Acetone switches to glucose that was converted and stored for energy reserves, including within fat.
If this occurs, the liver will begin breaking down fat reserves.
In the process of doing this, the body makes ketones as a byproduct.

Acetone is a type of ketone.
Once the body begins producing excess ketones, this state is known as ketosis.
Being in ketosis can be safe or even beneficial for some people. For example, the ketogenic (keto) diet deliberately induces a state of ketosis.
There is evidence this can reduce seizures in children with epilepsy, and research into potential benefits for other conditions is ongoing.

But having too many ketones is dangerous, especially for people with diabetes mellitus.
High levels of ketones can be associated with an increase in the acidity of a person’s blood.
This may lead to diabetic ketoacidosis (DKA), a serious complication that can cause a diabetic coma or death.

SYNONYM:
2-propanone
propanone
67-64-1
Dimethyl ketone
propan-2-one
Methyl ketone
Dimethylformaldehyde
Pyroacetic ether
beta-Ketopropane
Dimethylketal
Chevron acetone
Ketone propane
Pyroacetic acid
Ketone, dimethyl
dimethylketone2-Propanon
2-PROPANONE
2-Propanone
2-propanone
Aceton
Aceton, Dimethylketon
Acetona
Acetone
acetone

About Acetone Helpful information:
Acetone is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 000 to < 10 000 000 tonnes per annum.
Acetone is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Consumer Uses of acetone:
Acetone is used in the following products: coating products, anti-freeze products, lubricants and greases, adhesives and sealants, fillers, putties, plasters, modelling clay, non-metal-surface treatment products, washing & cleaning products, finger paints, polishes and waxes and air care products.
Other release to the environment of Acetone is likely to occur from: outdoor use and indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Article service life
Other release to the environment of Acetone is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)).
Acetone can be found in complex articles, with no release intended: vehicles and machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines). This substance can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), rubber (e.g. tyres, shoes, toys), plastic used for furniture & furnishings, including furniture coverings and fabrics, textiles and apparel used for furniture & furnishings, including furniture coverings (e.g. sofa covers, car seat covers, fabric chair, hammock).

Widespread uses by professional workers of Acetone:
Acetone is used in the following products: biocides (e.g. disinfectants, pest control products), coating products, washing & cleaning products, polymers, laboratory chemicals and adhesives and sealants.
Acetone is used in the following areas: mining, scientific research and development and agriculture, forestry and fishing.
Acetone is used for the manufacture of: chemicals, plastic products, machinery and vehicles, wood and wood products, fabricated metal products, electrical, electronic and optical equipment, pulp, paper and paper products and furniture.
Other release to the environment of Acetone is likely to occur from: outdoor use and indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Formulation or re-packing of Acetone:
Acetone is used in the following products: adhesives and sealants, laboratory chemicals, biocides (e.g. disinfectants, pest control products), coating products, fillers, putties, plasters, modelling clay, lubricants and greases, plant protection products, pharmaceuticals, polishes and waxes, washing & cleaning products and cosmetics and personal care products.
Release to the environment of Acetone can occur from industrial use: formulation of mixtures, manufacturing of the substance, in processing aids at industrial sites and as an intermediate step in further manufacturing of another substance (use of intermediates).

Uses at industrial sites of Acetone:
Acetone is used in the following products: washing & cleaning products, laboratory chemicals, photo-chemicals, cosmetics and personal care products, pharmaceuticals, biocides (e.g. disinfectants, pest control products), coating products and polymers.
Acetone is used in the following areas: mining.
Acetone is used for the manufacture of: chemicals, machinery and vehicles, electrical, electronic and optical equipment, furniture, plastic products and pulp, paper and paper products.
Release to the environment of Acetone can occur from industrial use: in processing aids at industrial sites, as processing aid, as an intermediate step in further manufacturing of another substance (use of intermediates) and in the production of articles.

Manufacture of Acetone:
Release to the environment of Acetone can occur from industrial use: manufacturing of the substance.

acetone
2-propanone
propanone
67-64-1
propan-2-one
Dimethyl ketone
Methyl ketone
Pyroacetic ether
Dimethylformaldehyde
beta-Ketopropane
Dimethylketal
Chevron acetone
Ketone propane
Aceton
Pyroacetic acid
Ketone, dimethyl
dimethylketone
RCRA waste number U002
Dimethyl formaldehyde
FEMA No. 3326
Aceton [German, Dutch, Polish]
Ketone, dimethyl-
.beta.-Ketopropane
Acetone [NF]
NSC 135802
UNII-1364PS73AF
MFCD00008765
(CH3)2CO
CHEBI:15347
1364PS73AF
Acetone (NF)
NSC-135802
NCGC00091179-01
DSSTox_CID_1482
DSSTox_RID_76176
Acetone (natural)
DSSTox_GSID_21482
Caswell No. 004
Acetone, for HPLC, >=99.8%
Acetone, for HPLC, >=99.9%
Acetone, ACS reagent, >=99.5%
CAS-67-64-1
HSDB 41
CCRIS 5953
ACETONE (1,1,1,3,3,3-D6)
EINECS 200-662-2
UN1090
RCRA waste no. U002
EPA Pesticide Chemical Code 004101
dimethylcetone
isopropanal
methylketone
Dimethylketon
Propanon
Sasetone
methyl-ketone
Taimax
2propanone
b-Ketopropane
AI3-01238
2-propanal
Acetone HP
Acetone ACS
Acetone, puriss.
Acetone p.A.
Acetone (TN)
Acetone HPLC grade
methyl methyl ketone
Acetone, for HPLC
Acetone, ACS reagent
Acetone, HPLC Grade
Acetone, technical grade
Acetone oil (Salt/Mix)
CH3COCH3
Acetone Reagent Grade ACS
Acetone, histological grade
EC 200-662-2
Acetone, analytical standard
Acetone, Environmental Grade
Acetone, Semiconductor Grade
Acetone, LR, >=99%
Acetone, natural, >=97%
UN 1091 (Salt/Mix)
Aceton (GERMAN, POLISH)
Acetone, puriss., 99.0%
CHEMBL14253
Dimethylketone, Pyroacetic acid
WLN: 1V1
Acetone, AR, >=99.5%
DTXSID8021482
Acetone, Spectrophotometric Grade
Citronellidene Acetone; Baccartol
ZINC895111
Acetone, GC, for residue analysis
Acetone, >=99.5%, ACS reagent
Tox21_111096
Tox21_202480
c0556
LMFA12000057
NSC135802
Acetone 5000 microg/mL in Methanol
Acetone, purum, >=99.0% (GC)
AKOS000120890
Acetone 100 microg/mL in Acetonitrile
UN 1090
Acetone, SAJ first grade, >=99.0%
Acetone [UN1090] [Flammable liquid]
Acetone, for chromatography, >=99.8%
Acetone, histological grade, >=99.5%
Acetone, JIS special grade, >=99.5%
Acetone, Laboratory Reagent, >=99.5%
NCGC00260029-01
Acetone, for HPLC, >=99.8% (GC)
Acetone, UV HPLC spectroscopic, 99.8%
Acetone, >=99.5%, for residue analysis
Acetone, for residue analysis, >=99.5%
A0054
Acetone, for luminescence, >=99.5% (GC)
FT-0621803
Acetone, suitable for determination of dioxins
Acetone, glass distilled HRGC/HPLC trace grade
C00207
D02311
Q49546
Acetone, ACS spectrophotometric grade, >=99.5%
Acetone, ReagentPlus(R), phenol free, >=99.5%
Acetone, >=99%, meets FCC analytical specifications
Acetone, ACS reagent, >=99.5%, <=2 ppm low benzene
Acetone, contains 20.0 % (v/v) acetonitrile, for HPLC
Acetone, for residue analysis, suitable for 5000 per JIS
UNII-N4G9GAT76C component CSCPPACGZOOCGX-UHFFFAOYSA-N
Acetone, for UV-spectroscopy, ACS reagent, >=99.7% (GC)
Acetone, United States Pharmacopeia (USP) Reference Standard
Acetone solution, contains 20.0 % (v/v) acetonitrile, for HPLC
Acetone, HPLC Plus, for HPLC, GC, and residue analysis, >=99.9%
Acetone, semiconductor grade MOS PURANAL(TM) (Honeywell 17921)
Acetone, semiconductor grade ULSI PURANAL(TM) (Honeywell 17014)
Acetone, semiconductor grade VLSI PURANAL(TM) (Honeywell 17617)
Acetone, Pharmaceutical Secondary Standard; Certified Reference Material
Acetone solution, certified reference material, 2000 mug/mL in methanol: water (9:1)
Acetone, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5% (GC)
Acetone, puriss., meets analytical specification of Ph. Eur., BP, NF, >=99% (GC)

Regulatory process names
2-Propanone
Aceton
Acetone
ACETONE
Acetone
acetone
Acetone (natural)
acetone; propan-2-one; propanone
beta-Ketopropane
Chevron acetone
Dimethyl ketone
Dimethylformaldehyde
Dimethylketal
Ketone propane
Ketone, dimethyl
Methyl ketone
propan-2-one
Propanone
propanone
Pyroacetic acid
Pyroacetic ether
Reaction mass of ethylbenzene and heptan-2-one and xylene and [[]3-(2,3-epoxypropoxy)propyl]trimethoxysilane and 2-ethyl-2-[[][[](1-oxoallyl)oxy]methyl]-1,3-propanediyl diacrylate and 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane

Translated names
2- Propanon (de)
2-propanone (it)
Aceton (de)
aceton (hr)
aceton (hu)
aceton (nl)
aceton (no)
aceton (pl)
aceton (sl)
aceton (sv)
acetona (es)
acetona (pt)
acetonas (lt)
acetone (cs)
acetone (da)
acetone (it)
acetons (lv)
acetonă (mt)
acetonă (ro)
Asetoni (fi)
atsetoon (et)
keton dimetylowy (pl)
propaan-2-on (nl)
propaan-2-oon (et)
propan 2-onă (mt)
propan 2-onă (ro)
propan-2-on (cs)
propan-2-on (da)
propan-2-on (hr)
propan-2-on (no)
propan-2-on (pl)
propan-2-on (sl)
propan-2-on (sv)
propan-2-ona (es)
propan-2-ona (pt)
propan-2-oni (fi)
propane-2-one (fr)
propanon (cs)
propanon (da)
Propanon (de)
propanon (hr)
propanon (hu)
propanon (nl)
propanon (pl)
propanon (sl)
propanon (sv)
propanona (es)
propanona (pt)
propanonas (lt)
propanone (fr)
propanone (it)
propanoni (fi)
propanons (lv)
propanonă (mt)
propanonă (ro)
propanoon (et)
propán-2-on (hu)
propán-2-ón (sk)
propān-2-ons (lv)


CAS names
2-Propanone

IUPAC names
2-PROPANONA
2-Propanone
2-propanone
Aceton
aceton
ACETONE
Acetone
acetone
Acetone
acetone
acetone / propan-2-one / propanone
acetone propan-2-one propanone
acetone.
acetone/propan-2-one/propanone
acetone; propan-2-one; propanone
actone
dimethlyketone
Dimethyl ketone
Dimethyl ketone, Propanone, 2-Propanone
Dimethylketon
isopropyl alcohol
propan-2-on
PROPAN-2-ONA
Propan-2-one
propan-2-one
propan-2-one propanone
propane-2-one
propanon
Propanone
propanone
2-Propanon
2-PROPANONE
2-Propanone
2-propanone
Aceton
Aceton, Dimethylketon
Acetona
Acetone
acetone
Acetone oil
Acetone premium, I, II grade)
ACETONE, 2-PROPANONE
ACETONE, DIMETHYLKETONE
Acetone; dimethyl ketone; methyl ketone
Beta-ketopropane
Clearweld Solution (Acetone)
DIMETHYL KETONE
Dimethyl Ketone
Dimethyl ketone
dimethyl ketone
dimethyl ketone; ketone propane; methyl ketone; propanone
Dimethylformaldehyd
DIMETHYLKETON
Dimethylketon
DIMETHYLKETON, 2-PROPANON
Dimethylketone
dimethylketone
Dimethylketone; Propanon-2
DIMETIL CETONA
DIMETILCHETONE
DMK
ETER PIROACETICO
Industrial Acetone
Ketone propane
ketone propane
Ketone, dimethyl
Ketopropan
Methyl ketone
propan-2-one
Propanon
PROPANON-2
Propanon-2
PROPANONA
Propanone
propanone
Propanone-2
Pyroacetic ether
ACETONE
Acetone (also known as propanone, dimethyl ketone, 2-propanone, propan-2-one and β-ketopropane) is the simplest representative of the group of chemical compounds known as ketones.
Acetone is a colorless, volatile, flammable liquid.
Acetone is miscible with water and serves as an important laboratory solvent for cleaning purposes.

CAS: 67-64-1
MF: C3H6O
MW: 58.08
EINECS: 200-662-2

Synonyms
ACETONE ALCOHOL;GRAMS DECOLORIZER;GRAM STAIN NO3;(CH3)2CO;2Propanon;ketone,dimethyl;ketonepropane;-Ketopropane;acetone;2-propanone;propanone;67-64-1;Dimethyl ketone;propan-2-one;Pyroacetic ether;Methyl ketone;Dimethylformaldehyde;beta-Ketopropane;Dimethylketal;Chevron acetone;Ketone propane;Aceton;Pyroacetic acid;Ketone, dimethyl;dimethylketone;Acetone (natural);FEMA No. 3326;Dimethyl formaldehyde;RCRA waste number U002;Taimax;Caswell No. 004;HSDB 41;dimethylcetone;Dimethylketon;CCRIS 5953;Propanon;Azeton;NSC 135802;Aceton [German, Dutch, Polish];EINECS 200-662-2;Ketone, dimethyl-;.beta.-Ketopropane;Acetone [NF];EPA Pesticide Chemical Code 004101;NSC-135802;UNII-1364PS73AF;DTXSID8021482;CHEBI:15347;AI3-01238;1364PS73AF;MFCD00008765;(CH3)2CO;DTXCID101482;EC 200-662-2;Acetone (NF);NSC135802;NCGC00091179-01;ACETONE (MART.);ACETONE [MART.];ACETONE (EP IMPURITY);ACETONE [EP IMPURITY];ACETONE (EP MONOGRAPH);ACETONE [EP MONOGRAPH];Acetona;Acetone, for HPLC, >=99.8%;Acetone, for HPLC, >=99.9%;Acetone, ACS reagent, >=99.5%;CAS-67-64-1;ISOFLURANE IMPURITY F (EP IMPURITY);ISOFLURANE IMPURITY F [EP IMPURITY];CHLOROBUTANOL IMPURITY B (EP IMPURITY);CHLOROBUTANOL IMPURITY B [EP IMPURITY];ACETONE (1,1,1,3,3,3-D6);UN1090;RCRA waste no. U002;isopropanal;methylketone;Sasetone;methyl-ketone;2propanone;b-Ketopropane;2-propanal;Acetone ACS;Acetone (TN);Acetone HPLC grade;methyl methyl ketone;Acetone, for HPLC
;Acetone, ACS reagent;Acetone, HPLC Grade;TAK - Toxic Alcohols;ACETONE [VANDF];ACETONE [FHFI];ACETONE [HSDB];Acetone ACS low benzene;ACETONE [FCC];ACETONE [MI];CH3COCH3;ACETONE [USP-RS];ACETONE [WHO-DD];Acetone, histological grade;Acetone, analytical standard;Acetone, Environmental Grade;Acetone, Semiconductor Grade;Acetone, LR, >=99%;Acetone, natural, >=97%;UN 1091 (Salt/Mix);Aceton (GERMAN, POLISH);Acetone, puriss., 99.0%;CHEMBL14253;WLN: 1V1;Acetone, AR, >=99.5%;Acetone (water < 1000 ppm);Acetone, Spectrophotometric Grade;Acetone, >=99.5%, ACS reagent;Tox21_111096;Tox21_202480;c0556;LMFA12000057;Acetone 5000 microg/mL in Methanol;Acetone, purum, >=99.0% (GC);AKOS000120890;ACETONE (2-13C, 99%);Acetone 100 microg/mL in Acetonitrile;UN 1090;Acetone, SAJ first grade, >=99.0%;USEPA/OPP Pesticide Code: 044101;Acetone [UN1090] [Flammable liquid];Acetone, for chromatography, >=99.8%;Acetone, histological grade, >=99.5%;Acetone, JIS special grade, >=99.5%;Acetone, Laboratory Reagent, >=99.5%;NCGC00260029-01;Acetone, for HPLC, >=99.8% (GC);Acetone, UV HPLC spectroscopic, 99.8%
;DESFLURANE IMPURITY H [EP IMPURITY];A0054;ACETONE (1,3-13C2, 99%);Acetone, for luminescence, >=99.5% (GC);FT-0621803;InChI=1/C3H6O/c1-3(2)4/h1-2H;NS00003196;Acetone, suitable for determination of dioxins;Acetone, glass distilled HRGC/HPLC trace grade;C00207;D02311;Q49546;Acetone, ACS spectrophotometric grade, >=99.5%;Acetone, ReagentPlus(R), phenol free, >=99.5%;TAS - Toxic alcohols in Human serum (Quantitative);Acetone, >=99%, meets FCC analytical specifications;Acetone, ACS reagent, >=99.5%, <=2 ppm low benzene;Acetone, contains 20.0 % (v/v) acetonitrile, for HPLC;Flavor and Extract Manufacturers' Association Number 3326;Acetone, for UV-spectroscopy, ACS reagent, >=99.7% (GC);Acetone, United States Pharmacopeia (USP) Reference Standard;Acetone, semiconductor grade MOS PURANAL(TM) (Honeywell 17921);Acetone, semiconductor grade ULSI PURANAL(TM) (Honeywell 17014);Acetone, semiconductor grade VLSI PURANAL(TM) (Honeywell 17617)

Acetone is a highly effective solvent for many organic compounds such as Methanol, ethanol, ether, chloroform, pyridine, etc., and is the active ingredient in nail polish remover.
Acetone is also used to make various plastics, fibers, drugs, and other chemicals.
Acetone exists in nature in the Free State.
In the plants, Acetone mainly exists in essential oils, such as tea oil, rosin essential oil, citrus oil, etc.; human urine and blood and animal urine, marine animal tissue and body fluids contain a small amount of acetone.
Acetone is a flammable, colorless liquid with a pleasant odor.

Acetone is used widely as an organic solvent and in the chemical industry.
Acetone is the simplest ketone, which also goes by the name dimethyl ketone (DMK).
Acetone was originally referred to as pyroacetic spirit because it was obtained from the destructive distillation of acetates and acetic acid.
A methyl ketone that consists of propane bearing an oxo group at C2.
Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH3)2CO.
Acetone is the simplest and smallest ketone (>C=O).
Acetone is a colorless, highly volatile, and flammable liquid with a characteristic pungent odor.

Acetone is miscible with water and serves as an important organic solvent in industry, home, and laboratory.
About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and for production of methyl methacrylate and bisphenol A, which are precursors to widely used plastics.
Acetone is a common building block in organic chemistry.
Acetone serves as a solvent in household products such as nail polish remover and paint thinner.
Acetone has volatile organic compound (VOC)-exempt status in the United States.

Acetone is produced and disposed of in the human body through normal metabolic processes.
Acetone is normally present in blood and urine.
People with diabetic ketoacidosis produce it in larger amounts.
Ketogenic diets that increase ketone bodies (acetone, β-hydroxybutyric acid and acetoacetic acid) in the blood are used to counter epileptic attacks in children who suffer from refractory epilepsy.

Name
From the 17th century, and before modern developments in organic chemistry nomenclature, acetone was given many different names.
They included "spirit of Saturn", which was given when Acetone was thought to be a compound of lead and, later, "pyro-acetic spirit" and "pyro-acetic ester".
Prior to the name "acetone" being coined by the French chemist Antoine Bussy, it was named "mesit" (from the Greek μεσίτης, meaning mediator) by Carl Reichenbach, who also claimed that methyl alcohol consisted of mesit and ethyl alcohol.
Names derived from mesit include mesitylene and mesityl oxide which were first synthesised from acetone.
Unlike many compounds with the acet- prefix which have a 2-carbon chain, acetone has a 3-carbon chain.
That has caused confusion because there cannot be a ketone with 2 carbons.
The prefix refers to acetone's relation to vinegar (acetum in Latin, also the source of the words "acid" and "acetic"), rather than its chemical structure.

History
The traditional method of producing acetone in the 19th century and the beginning of the 20th century was to distill acetates, particularly calcium acetate, Ca(C2H3O2)2.
Weizmann discovered a process to produce butyl alcohol and acetone from the bacterium Clostridium acetobutylicum in 1914.
With England’s urgent demand for acetone, Winston Churchill (1874–1965) enlisted Weizmann to develop the Weizmann process for acetone production on an industrial scale.
Fermentation and distillation techniques for acetone production were replaced starting in the 1950s with the cumene oxidation process.
In this process, cumene is oxidized to cumene hydroperoxide, which is then decomposed using acid to acetone and phenol.
Acetone is the primary method used to produce phenol, and acetone is produced as a co-product in the process, with a yield of about 0.6:1 of acetone to phenol.

Acetone Chemical Properties
Melting point: -94 °C(lit.)
Boiling point: 56 °C760 mm Hg(lit.)
Density: 0.791 g/mL at 25 °C(lit.)
Vapor density: 2 (vs air)
Vapor pressure: 184 mm Hg ( 20 °C)
Refractive index: n20/D 1.359(lit.)
FEMA: 3326 | ACETONE
Fp: 1 °F
Storage temp.: Store at +5°C to +30°C.
Solubility: Miscible with water and with ethanol (96 per cent).
pka: 19.3(at 25℃)
Form: Liquid
Color: Colorless, invisible vapor
Specific Gravity: 0.79 (25/25℃)
Odor: Characteristic pungent odor detectable at 33 to 700 ppm (mean = 130 ppm)
PH: 5-6 (395g/l, H2O, 20°C)
Relative polarity: 0.355
Odor Threshold: 42ppm
Odor Type: solvent
Explosive limit: 2.6-12.8%(V)
Water Solubility: soluble
Merck: 14,66
JECFA Number: 139
BRN: 63580
Henry's Law Constant: 2.27 at 14.9 °C, 3.03 at 25 °C, 7.69 at 35.1 °C, 11.76 at 44.9 °C (Betterton, 1991)
Exposure limits TLV-TWA 1780 mg/m3 (750 ppm), STEL 2375 mg/m3 (ACGIH); 10 h–TWA 590 mg/m3 (250 ppm); IDLH 20,000 ppm (NIOSH).
Dielectric constant: 1.0(0℃)
LogP: -0.160
CAS DataBase Reference: 67-64-1(CAS DataBase Reference)
NIST Chemistry Reference: Acetone(67-64-1)
EPA Substance Registry System: Acetone (67-64-1)

Acetone, CH3COCH3, also known as 2-propanone and dimethylketone, is a colorless, volatile,flammable liquid that boils at 56°C (133 OF).
Acetone is misciblewith water and is oftenused as a solventin the manufacture of lacquers and paints.
Clear, colorless, liquid with a sweet, fragrant odor. Sweetish taste.
Odor threshold concentrations ranged from 42 ppmv to 100 ppmv.
Experimentally determined detection and recognition odor threshold concentrations were 48 mg/m3 (20 ppmv) and 78 mg/m3 (33 ppmv), respectively.
The flame temperature of pure acetone is 1980 °C.

Like most ketones, Acetone exhibits the keto–enol tautomerism in which the nominal keto structure (CH3)2C=O of acetone itself is in equilibrium with the enol isomer (CH3)C(OH)=(CH2) (prop-1-en-2-ol).
In acetone vapor at ambient temperature, only 2.4×10−7% of the molecules are in the enol form.
In the presence of suitable catalysts, two acetone molecules also combine to form the compound diacetone alcohol (CH3)C=O(CH2)C(OH)(CH3)2, which on dehydration gives mesityl oxide (CH3)C=O(CH)=C(CH3)2.
Acetone can further combine with another acetone molecule, with loss of another molecule of water, yielding phorone and other compounds.
Acetone is a weak Lewis base that forms adducts with soft acids like I2 and hard acids like phenol.
Acetone also forms complexes with divalent metals.

Uses
Industrial
About a third of the world's acetone is used as a solvent, and a quarter is consumed as acetone cyanohydrin, a precursor to methyl methacrylate.

Solvent
Acetone is a good solvent for many plastics and some synthetic fibers.
Acetone is used for thinning polyester resin, cleaning tools used with it, and dissolving two-part epoxies and superglue before they harden.
Acetone is used as one of the volatile components of some paints and varnishes.
As a heavy-duty degreaser, Acetone is useful in the preparation of metal prior to painting or soldering, and to remove rosin flux after soldering (to prevent adhesion of dirt and electrical leakage and perhaps corrosion or for cosmetic reasons), although Acetone may attack some electronic components, such as polystyrene capacitors.

Although itself flammable, acetone is used extensively as a solvent for the safe transportation and storage of acetylene, which cannot be safely pressurized as a pure compound.
Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone. One litre of acetone can dissolve around 250 litres of acetylene at a pressure of 10 bars (1.0 MPa).
Acetone is used as a solvent by the pharmaceutical industry and as a denaturant in denatured alcohol.
Acetone is also present as an excipient in some pharmaceutical drugs.

Medical
Dermatologists use acetone with alcohol for acne treatments to chemically peel dry skin.
Common agents used today for chemical peeling are salicylic acid, glycolic acid, azelaic acid, 30% salicylic acid in ethanol, and trichloroacetic acid (TCA).
Prior to chemexfoliation, the skin is cleaned and excess fat removed in a process called defatting.
Acetone, hexachlorophene, or a combination of these agents was used in this process.

Acetone has been shown to have anticonvulsant effects in animal models of epilepsy, in the absence of toxicity, when administered in millimolar concentrations.
Acetone has been hypothesized that the high-fat low-carbohydrate ketogenic diet used clinically to control drug-resistant epilepsy in children works by elevating acetone in the brain.
Because of their higher energy requirements, children have higher acetone production than most adults – and the younger the child, the higher the expected production.
This indicates that children are not uniquely susceptible to acetone exposure. External exposures are small compared to the exposures associated with the ketogenic diet.

Domestic and other niche uses
Make-up artists use acetone to remove skin adhesive from the netting of wigs and mustaches by immersing the item in an acetone bath, then removing the softened glue residue with a stiff brush.
Acetone is a main ingredient in many nail polish removers because it breaks down nail polish.
Acetone is used for all types of nail polish removal, like gel nail polish, dip powder and acrylic nails.

Acetone is often used for vapor polishing of printing artifacts on 3D-printed models printed with ABS plastic.
The technique, called acetone vapor bath smoothing, involves placing the printed part in a sealed chamber containing a small amount of acetone, and heating to around 80 degrees Celsius for ten minutes.
This creates a vapor of acetone in the container.
The acetone condenses evenly all over the part, causing the surface to soften and liquefy.
Surface tension then smooths the semi-liquid plastic.
When the part is removed from the chamber, the acetone component evaporates leaving a glassy-smooth part free of striation, patterning, and visible layer edges, common features in untreated 3D printed parts.
Acetone efficiently removes felt-tipped pen marks from glass and metals.

An important organic raw material in the chemical, artificial fiber, medicine, paint, plastics, organic glass, cosmetics and other industries; an excellent organic solvent that dissolves many organic products such as resin, cellulose acetate, acetylene and so on.
An important raw material for the synthesis of ketene, acetic anhydride, iodoform, polyisoprene rubber, methacrylic acid, methyl ester, chloroform, and epoxy resins.
The acetone cyanohydrin obtained from the reaction of acetone with hydrocyanic acid is the raw material of methacrylic resin (perspex).
A raw material in the production of epoxy resin intermediate bisphenol A.
In pharmaceuticals, acetone is used as extractants for a variety of vitamins and hormones in addition to vitamin C, and dewaxing solvents for petroleum refining.
A raw material for nail polish remover in cosmetics
One of the raw materials for synthesizing pyrethroids in pesticide industry
Acetone is often used to wipe the black ink above the copper tube in the precision copper tube industry.

Acetone is used in the chemical industry in numerous applications.
The primary use of acetone is to produce acetone cyanohydrin, which is then used in the production of methyl methacrylate (MMA).
Another use of acetone in the chemical industry is for bisphenol A (BPA).
BPA results form the condensation reaction of acetone and phenol in the presence of an appropriate catalyst.
BPA is used in polycarbonate plastics, polyurethanes, and epoxy resins.
Polycarbonate plastics are tough and durable and are often used as a glass substitute.
In addition to its use as a chemical feedstock and intermediate, acetone is used extensively as an organic solvent in lacquers, varnishes, pharmaceuticals, and cosmetics.
Nail polish remover is one of the most common products containing acetone.
Acetone is used to stabilize acetylene for transport .
Acetone is used in the manufacture of a largenumber of compounds, such as acetic acid,chloroform, mesityl oxide, and MIBK; in themanufacture of rayon, photographic films, and explosives; as a common solvent; inpaint and varnish removers; and for purifyingparaffins.

Solvent for fats, oils, waxes, resins, rubber, plastics, lacquers, varnishes, rubber cements.
manufacture of methyl isobutyl ketone, mesityl oxide, acetic acid (ketene process), diacetone alcohol, chloroform, iodoform, bromoform, explosives, aeroplane dopes, rayon, photographic films, isoprene; storing acetylene gas (takes up about 24 times its vol of the gas); extraction of various principles from animal and plant substances; in paint and varnish removers; purifying paraffin; hardening and dehydrating tissues.
Pharmaceutic aid (solvent).
Acetone′s luminesence intensity is dependent upon the solution component.
The absorption of UV light by acetone, results in its photolysis and the production of radials.
Acetone is a solvent considered to be non-comedogenic and occasionally used in skin toners.
Acetone is primarily used in nail polish remover.
Acetone could be drying and very irritating to the skin depending on the concentration and frequency of use.

Industrial uses
Acetone is valuable solvent component in acrylic/nitrocellulose automotive lacquers.
Acetone is the solvent of choice in film coatings operations which use vinylidene chloride-acrylonitrile copolymer formulations.
Other ketones that may be used in these film coating operations include methyl isobutyl ketone, ethyl n-amyl ketone, and diisobutyl ketone.
Acetone, blends of MIBK and MEK, methyl namyl ketone, ethyl n-amyl ketone, and diisobutyl ketone are all useful solvents for vinyl resin copolymers.
The presence of one of the slower evaporating ketones in the solvent blend prevents quick drying, improves flow, and gives blush resistance to the coating.

Acetone is also used as a resin thinner in polyester resins and as a clean up solvent for the resin reactor kettle.
In solvents industry, Acetone is a component of solvent blends in urethane, nitrile rubber, and neoprene industrial adhesives.
Acetone is the primary solvent in resin-type adhesives and pressure sensitive chlorinated rubber adhesives.
Acetone also can be used to extract fats, oils, waxes, and resins from natural products, to dewax lubricating oils, and to extract certain essential oils.
Acetone is also an important chemical intermediate in the preparation of several oxygenated solvents including the ketones, diacetone alcohol, mesityl oxide, methyl isobutyl ketone, and isophorone.

Production
In 1913, the United Kingdom developed a method for fermenting cereals to produce acetone and butanol.
In 1920, the dehydrogenation of isopropanol (synthesized by hydration of propylene) appeared.
From 1953 to 1955, the United States Hercules and the British Distilling Company jointly developed the cumene process method, thereafter, Japan, the United Kingdom, and the Netherlands also developed other methods.
Now, Most of the worldwide industrial production of acetone (and phenol) is based on the cumene process, which uses benzene and propylene as raw materials, via cumene intermediates, then oxidized, hydrolyzed to produce acetone and co-produced phenol.
Acetone is obtained by fermentation as a by-product of n-butyl alcohol manufacture, or by chemical synthesis from isopropyl alcohol; from cumene as a by-product in phenol manufacture; or from propane as a by-product of oxidation-cracking.
Acetone can also be produced from isopropanol using several methods, but the main methodis by catalytic dehydrogenation.

Acetone Reaction
Acetone is mainly used as an organic solvent and methyl methacrylate (the main raw material for organic glass).
In the United States and Western Europe, the two accounts for 70% of the total consumption.
Acetone is used for bisphenol A, accounting for 10% to 15%, and the others 15% % to 20%.

Health Effects
Summary: Acetone is mainly responsible for the inhibition and anesthesia of the central nervous system and exposure to high concentrations may cause liver, kidney, and pancreas impair to particular people.
Because of its low toxicity, rapid metabolism and detoxification, acute poisoning under production conditions is rare.
In case acute poisoning happens, symptoms of vomiting, shortness of breath, paralysis, and even coma can occur.
After oral administration, burning sensation in the lips and throat may occur after hours of incubation, such as dry mouth, vomiting, drowsiness, acidity and ketosis, and even temporary disturbance of consciousness.
The long-term damage of acetone to the human body is manifested as irritation to the eyes such as tearing, photophobia and infiltration of the corneal epithelium, as well as dizziness, burning sensation, throat irritation, and coughing.

Metabolism in the body: After being absorbed by the lungs, gastrointestinal tract, and skin, acetone is easily absorbed into the bloodstream due to its high water solubility and is rapidly distributed throughout the body.
The excretion depends on the dose. When the dose is large, the main tract is mainly through the lungs and kidneys, and a very small amount is discharged through the skin.
When the dose is small, most of them are oxidized into carbon dioxide.
The biological half-life of acetone in blood is 5.3 h for rats, 11 h for dogs, and 3 h for humans.
The metabolites of acetone in the human body are mostly a tricarboxylic acid cycle intermediate that is decomposed to acetoacetate and converted to glycogen.

Reactivity Profile
Acetone was reported that a mixture of Acetone and chloroform, in a residue bottle, exploded.
Since addition of Acetone to chloroform in the presence of base will result in a highly exothermic reaction, Acetone is thought that a base was in the bottle.
Also, Nitrosyl chloride, sealed in a tube with a residue of Acetone in the presence of platinum catalyst, gave an explosive reaction.
The reaction of nitrosyl perchlorate and Acetone ignites and explodes.
Explosions occur with mixtures of nitrosyl perchlorate and primary amine.
Reacts violently with nitric acid.
Also causes exothermic reaction when in contact with aldehydes.

Health Hazard
The acute toxicity of acetone is low. Acetone is primarily a central nervous system depressant at high concentrations (greater than 12,000 ppm).
Unacclimated volunteers exposed to 500 ppm acetone experienced eye and nasal irritation, but Acetone has been reported that 1000 ppm for an 8-hour day produced no effects other than slight transient irritation to eyes, nose, and throat.
Therefore there are good warning properties for those unaccustomed to working with acetone; however, frequent use of acetone seems to cause accommodation to its slight irritating properties.
Acetone is practically nontoxic by ingestion.
A case of a man swallowing 200 mL of acetone resulted in his becoming stuporous after 1 hour and then comatose; he regained consciousness 12 hour later.
Acetone is slightly irritating to the skin, and prolonged contact may cause dermatitis.
Liquid acetone produces moderate transient eye irritation.
Acetone has not been found to be carcinogenic in animal tests or to have effects on reproduction or fertility.

Fire Hazard
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.
Vapors may form explosive mixtures with air.
Vapors may travel to source of ignition and flash back.
Most vapors are heavier than air.
They will spread along ground and collect in low or confined areas (sewers, basements, tanks).
Vapor explosion hazard indoors, outdoors or in sewers.
Runoff to sewer may create fire or explosion hazard.
Containers may explode when heated. Many liquids are lighter than water.

Purification Methods
The commercial preparation of acetone by catalytic dehydrogenation of isopropyl alcohol gives relatively pure material.
Analytical reagent quality generally contains less than 1% of organic impurities but may have up to about 1% of H2O.
Dry acetone is appreciably hygroscopic.
The main organic impurity in acetone is mesityl oxide, formed by aldol condensation.
Acetone can be dried with anhydrous CaSO4, K2CO3 or type 4A Linde molecular sieves, and then distilled.
Silica gel and alumina, or mildly acidic or basic desiccants cause acetone to undergo the aldol condensation, so that its water content is increased by passage through these reagents.
Acetone also occurs to some extent when P2O5 or sodium amalgam is used.

Anhydrous MgSO4 is an inefficient drying agent, and CaCl2 forms an addition compound.
Drierite (anhydrous CaSO4) offers minimum acid and base catalysis for aldol formation and is the recommended drying agent for this solvent.
Acetone can be shaken with Drierite (25g/L) for several hours before it is decanted and distilled from fresh Drierite (10g/L) through an efficient column, maintaining atmospheric contact through a Drierite drying tube.
The equilibrium water content is about 10-2M.
Anhydrous Mg(ClO4)2 should not be used as drying agent because of the risk of EXPLOSION with acetone vapour.
Organic impurities have been removed from acetone by adding 4g of AgNO3 in 30mL of water to 1L of acetone, followed by 10mL of M NaOH, shaking for 10minutes, filtering, drying with anhydrous CaSO4 and distilling.
Alternatively, successive small portions of KMnO4 have been added to acetone at reflux, until the violet colour persists, followed by drying and distilling. Refluxing with chromium trioxide (CrO3) has also been used.

Acetone has been removed from acetone by azeotropic distillation (at 35o) with methyl bromide, and treatment with acetyl chloride.
Small amounts of acetone can be purified as the NaI addition compound, by dissolving 100g of finely powdered NaI in 400g of boiling acetone, then cooling in ice and salt to -8o.
Crystals of NaI.3Me2CO are filtered off and, on warming in a flask, acetone distils off readily.
Acetone has also been purified by gas chromatography on a 20% free fatty acid phthalate (on Chromosorb P) column at 100o.
For efficiency of desiccants in drying acetone see Burfield and Smithers.
The water content of acetone can be determined by a modified Karl Fischer titration.
Rapid procedure: Dry over anhydrous CaSO4 and distil.
ACETONITRILE
Acetonitrile is the chemical compound with the formula CH3CN.
This colorless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic).
Acetonitrile is produced mainly as a byproduct of acrylonitrile manufacture.

CAS Number: 75-05-8
EC number: 200-835-2
Molecular Formula: C2H3N
Molar Mass: 41.05 g/mol

Acetonitrile is one of the most frequently utilized eluents in reverse phase chromatographic purification of peptides, partially thanks to Acetonitrile low viscosity, high chemical stability and strong eluting power.
Moreover, Acetonitrile has also found widespread applications as a polar aprotic solvent in organic synthesis.

Acetonitrile is produced mainly as a byproduct of acrylonitrile manufacture via Sohio process by means of propylene ammoxidation.
In the acrylonitrile production with the aforementioned process hydrogen cyanide is released as a byproduct.

Pure acetonitrile is recovered by distillation from the waste before the treatment.
If residual hydrogen cyanide survives the intermediary purification steps Acetonitrile will contaminate the acetonitrile.

Moreover, in spite of Acetonitrile significant chemical stability acetonitrile does suffer from decomposition when heated or reacted with acid or oxidizing agents.
The pyrolysis or chemical degradation of acetonitrile will also lead to the formation of hydrogen cyanide.
Acetonitrile is know that cyanide could function with carbonyl derivatives, e.g., ketones or aldehydes, by means of nucleophilic addition to generate the corresponding cyanohydrin derivatives.

Acetonitrile is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.
Acetonitrile is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Acetonitrile is used as a solvent in the manufacture of pharmaceuticals.
Acetonitrile is also used in the organic synthesis of spinning fibers.

Acetonitrile is used as a solvent in the production of vitamin B, pharmaceuticals, perfumes, pesticides, plastics and as a non-aqueous solvent for inorganic salts.
Acetonitrile is also used in the photographic industry, in the extraction and refining of copper, in the textile industry, in lithium batteries, for the extraction of fatty acids from animal and vegetable oils, and in analytical chemistry laboratories.

Acetonitrile is used as a polar aprotic solvent in organic synthesis and in the purification of butadiene.

Acetonitrile is the chemical compound with the formula CH3CN.
This colorless liquid is the simplest organic nitrile.

Acetonitrile is produced mainly as a byproduct of acrylonitrile manufacture.
Acetonitrile is used as a polar aprotic solvent in organic synthesis and in the purification of butadiene.

In the laboratory, Acetonitrile is used as a medium-polarity solvent that is miscible with water and a range of organic solvents, but not saturated hydrocarbons.
Acetonitrile dissolves a wide range of ionic and nonpolar compounds and is useful as a mobile phase in HPLC and LC-MS.

Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula CH3CN and structure H3C−C≡N.
This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic).

Acetonitrile is produced mainly as a byproduct of acrylonitrile manufacture.
Acetonitrile is used as a polar aprotic solvent in organic synthesis and in the purification of butadiene.
The N≡C−C skeleton is linear with a short C≡N distance of 1.16 Å.

Acetonitrile was first prepared in 1847 by the French chemist Jean-Baptiste Dumas.

Acetonitrile is a nitrile that is hydrogen cyanide in which the hydrogen has been replaced by a methyl group.
Acetonitrile has a role as a polar aprotic solvent and an EC 3.5.1.4 (amidase) inhibitor.
Acetonitrile is an aliphatic nitrile and a volatile organic compound.

Acetonitrile has many uses, including as a solvent, for spinning fibers, and in lithium batteries.
Acetonitrile is primarily found in air from automobile exhaust and manufacturing facilities.

Acute (short-term) inhalation exposure results in irritation of mucous membranes.
Chronic (long-term) exposure results in central nervous system effects, such as headaches, numbness, and tremors.

No data are available on Acetonitrile carcinogenic effects in humans.
EPA has classified Acetonitrile as a Group D, not classifiable as to human carcinogenicity.

Acetonitrile, an aliphatic nitrile, is widely used as an organic solvent and intermediate in organic syntheses.
Acetonitrile is transparent to UV-visible light, which makes Acetonitrile highly applicable in spectrophotometric and fluorimetric techniques.

MeCN is utilized as a mobile phase component in many chromatographic techniques, due to Acetonitrile low viscosity, high elution strength and miscibility in water.
Acetonitrile also plays a major role as an extractant medium in liquid-liquid extraction, solid-phase extraction or microextraction.

Acetonitrile appears as a colorless limpid liquid with an aromatic odor.
Flash point 42 °F.
Density 0.783 g / cm3.
Toxic by skin absorption.
Less dense than water.
Vapors are denser than air.

Applications of Acetonitrile:
Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries.
Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, Acetonitrile absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.
Heat is then employed in the separating tower to separate the butadiene.

In the laboratory, Acetonitrile is used as a medium-polarity solvent that is miscible with water and a range of organic solvents, but not saturated hydrocarbons.
Acetonitrile has a convenient liquid range and a high dielectric constant of 38.8.
With a dipole moment of 3.92 D, acetonitrile dissolves a wide range of ionic and nonpolar compounds and is useful as a mobile phase in HPLC and LC–MS.

Acetonitrile is widely used in battery applications because of Acetonitrile relatively high dielectric constant and ability to dissolve electrolytes.
For similar reasons Acetonitrile is a popular solvent in cyclic voltammetry.

Acetonitrile ultraviolet transparency UV cutoff, low viscosity and low chemical reactivity make Acetonitrile a popular choice for high-performance liquid chromatography (HPLC).
Acetonitrile plays a significant role as the dominant solvent used in oligonucleotide synthesis from nucleoside phosphoramidites.
Industrially, Acetonitrile is used as a solvent for the manufacture of pharmaceuticals and photographic film.

Organic synthesis:
Acetonitrile is a common two-carbon building block in organic synthesis of many useful chemicals, including acetamidine hydrochloride, thiamine, and α-napthaleneacetic acid.
Acetonitrile reaction with cyanogen chloride affords malononitrile.

As an electron pair donor:
Acetonitrile has a free electron pair at the nitrogen atom, which can form many transition metal nitrile complexes.

Being weakly basic, Acetonitrile is an easily displaceable ligand.
For example, bis(acetonitrile)palladium dichloride is prepared by heating a suspension of palladium chloride in acetonitrile:
PdCl2+2CH3CN⟶PdCl2(CH3CN)2

A related complex is tetrakis(acetonitrile)copper(I) hexafluorophosphate [Cu(CH3CN)4]+.
The CH3CN groups in these complexes are rapidly displaced by many other ligands.

Acetonitrile also forms Lewis adducts with group 13 Lewis acids like boron trifluoride.
In superacids, Acetonitrile is possible to protonate acetonitrile.

Uses of Acetonitrile:
Acetonitrile is predominantly used as a solvent in the manufacture of pharmaceuticals, for spinning fibers and for casting and molding of plastic materials, in lithium batteries, for the extraction of fatty acids from animal and vegetable oils, and in chemical laboratories for the detection of materials such as pesticide residues.
Acetonitrile is used as a solvent for extraction of hydrocarbons, for separation of fatty acids from vegetable oils, and as a specialty solvent.

Acetonitrile is used solvent in hydrocarbon extraction processes, especially for butadiene such as specialty solvent, intermediate, catalyst, separation of fatty acids from vegetable oils, manufacturing of synthetic pharmaceuticals.

Acetonitrile is used in organic synthesis as starting material for acetophenone, alpha-naphthaleneacetic acid, thiamine, acetamidine.
Acetonitrile is used to remove tars, phenols, and coloring matter from petroleum hydrocarbons which are not soluble in acetonitrile.

Acetonitrile is used to extract fatty acids from fish liver oils and other animals and vegetable oils.
Acetonitrile is used polar solvent in non-aqueous titrations such as non-aqueous solvent for inorganic salts.

Acetonitrile is used in, UV, and electrochemistry applications.
Facilitates reactions between organic substrates and inorganic materials.

Acetonitrile may be used as a solvent to prepare:
1,2-Azidoalcohols and 1,2-azidoamines via cerium(III) chloride assisted ring opening of epoxides and aziridines by sodium azide.
Cyano-bearing indolinones by oxidative arylalkylation of olefins in the presence of palladium catalyst.

Acetonitrile may also be used as a reactant to synthesize:
Bis (diphenylphosphino) acetonitrile by reacting with n-butyllithium and then with chlorodiphenylphosphine.
β-Acetamido ketones via coupling reaction with ketones or ketoesters and aldehydes in the presence of cobalt(II) chloride.

Consumer Uses:
Acetonitrile is used in the following products: electrolytes for batteries.
Other release to the environment of Acetonitrile is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

Other Consumer Uses:
Intermediate
Intermediates
Laboratory chemicals
Solvent

Widespread uses by professional workers:
Acetonitrile is used in the following products: laboratory chemicals, extraction agents and photo-chemicals.
Acetonitrile is used in the following areas: scientific research and development, formulation of mixtures and/or re-packaging and health services.

Release to the environment of Acetonitrile can occur from industrial use: of substances in closed systems with minimal release, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and formulation of mixtures.
Other release to the environment of Acetonitrile is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Uses at industrial sites:
Acetonitrile is used in the following products: laboratory chemicals, extraction agents, pH regulators and water treatment products, pharmaceuticals and washing & cleaning products.
Acetonitrile has an industrial use resulting in manufacture of another substance (use of intermediates).

Acetonitrile is used in the following areas: scientific research and development.
Release to the environment of Acetonitrile can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), in processing aids at industrial sites, of substances in closed systems with minimal release, as processing aid and manufacturing of Acetonitrile.

Other Industry Uses:
Functional fluids (closed systems)
Intermediate
Intermediates
Laboratory chemicals
Solvent
Solvents (for cleaning or degreasing)

Industrial Processes with risk of exposure:
Semiconductor Manufacturing

Activities with risk of exposure:
Smoking cigarettes

Physical Properties of Acetonitrile:
Acetonitrile is a flammable colourless liquid with a sweet ether-like odour which is detectable at ppm levels.
Melting Point: -48°C
Boiling Point: 82°c
Specific Gravity: 0.786
Vapour Density: 1.41

Chemical Properties of Acetonitrile:
Acetonitrile is very soluble in water.
Acetonitrile mixes with most organic solvents, e.g. alcohols, esters, acetone, ether, benzene, chloroform, carbon tetrachloride and many unsaturated hydrocarbons.

Acetonitrile does not mix with petroleum ether and many saturated hydrocarbons.
Acetonitrile is incompatible with water, acids, bases, oleum, perchlorates, nitrating agents, reducing agents and alkali metals.

Acetonitrile decomposes on contact with acids, water and steam, producing toxic fumes and flammable vapour.
Acetonitrile reacts with strong oxidants such as nitric acid, chromic acid and sodium peroxide, causing fire and explosion hazards.

Acetonitrile forms toxic fumes of hydrogen cyanide and nitrogen oxides on combustion.
Acetonitrile attacks some forms of plastics, rubber and coatings.

Polymerization of Acetonitrile:
A mixture of acetonitrile and sulfuric acid on heating (or self-heating) to 53 °C underwent an uncontrollable exothermic reaction to 160 °C in a few seconds.
The presence of 28 mol% of sulfur trioxide reduces the initiation temperature to about 15 °C.
Polymerization of the nitrile is suspected.

Production of Acetonitrile:
Acetonitrile is a byproduct from the manufacture of acrylonitrile.
Most is combusted to support the intended process but an estimated several thousand tons are retained for the above-mentioned applications.

Production trends for acetonitrile thus generally follow those of acrylonitrile.
Acetonitrile can also be produced by many other methods, but these are of no commercial importance as of 2002.

Illustrative routes are by dehydration of acetamide or by hydrogenation of mixtures of carbon monoxide and ammonia.
In 1992, 14,700 tonnes (32,400,000 lb) of acetonitrile were produced in the US.

Catalytic ammoxidation of ethylene was also researched.

Acetonitrile shortage in 2008–2009:
Starting in October 2008, the worldwide supply of acetonitrile was low because Chinese production was shut down for the Olympics.
Furthermore, a U.S. factory was damaged in Texas during Hurricane Ike.

Due to the global economic slowdown, the production of acrylonitrile used in acrylic fibers and acrylonitrile butadiene styrene (ABS) resins decreased.
Acetonitrile is a byproduct in the production of acrylonitrile and its production also decreased, further compounding the acetonitrile shortage.
The global shortage of acetonitrile continued through early 2009.

Manufacturing Methods of Acetonitrile:
Acetonitrile is mainly prepared by dehydration of acetamide (CH3CONH2) with glacial acetic acid or by reacting acetic acid with ammonia at 400-500 °C in the presennce of a dehydration catalyst.

Acetonitrile and hydrogen cyanide are the principal byproducts from the ammoxidation of propylene to acrylonitrile (Sohio process).
Some acrylonitrile producers recover and purify acetonitrile, but most companies burn the byproducts as plant fuel.

Obtained commercially as a byproduct in manufacture of acrylonitrile.
Preparation by dehydration of acetamide.

General Manufacturing Information of Acetonitrile:

Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
All Other Chemical Product and Preparation Manufacturing
All other Petroleum and Coal Products Manufacturing
Pesticide, Fertilizer, and Other Agricultural Chemical Manufacturing
Petroleum Refineries
Pharmaceutical and Medicine Manufacturing
Plastics Material and Resin Manufacturing
Services
Wholesale and Retail Trade

Structure of Acetonitrile:
Acetonitrile is an organic molecule that is composed of carbon, hydrogen, and nitrogen atoms.
Acetonitrile is the simplest organic nitrile that is produced as a byproduct in acrylonitrile synthesis.

Acetonitrile is found in the environment mainly in the exhaust of automobiles and in the air in industrial sites.
A nitrile is an organic molecule whose functional group is the nitrile group −C≡N, which is composed of a single carbon atom sharing three pairs of electrons with a nitrogen atom.

The bond angles between the terminal carbon, the central carbon, and the nitrogen are all 180∘.
The reason why the bond angle between the central C and the N atoms is 180∘ is because of the presence of the triple bonds.

And the reason why the bond angle between the terminal C and the central C is also 180∘ is because this angle is perfect for minimizing the effects of electron repulsion.
Bonds are negatively charged electrons, and like repels like.
Which is why covalent bonds prefer to be as far apart as possible.

The hybridization of the terminal carbon atom −CH3 is sp3 while the hybridization of the central carbon atom is sp.
The hybridized sp orbital has 50% s character and 50% p character.

The sp3 orbital results from the hybridization of an s orbital and three p orbitals (p_x, p_y, p_z).
The sp3 orbital is 75% p character and 25% s character.

Sampling Procedures of Acetonitrile:
Measurements to determine employee exposure are best taken so that the avg 8 hr exposure is based on a single 8 hr sample or on two 4 hr samples.
Several short-time interval samples (up to 30 min) may also be used to determine the avg exposure level.

Air samples should be taken in the employee's breathing zone.
Sampling may be performed by collection of acetonitrile vapors using an adsorption tube.

Analytic Laboratory Methods of Acetonitrile:

Method: NIOSH 1606, Issue 3
Procedure: gas chromatography with flame ionization detector
Analyte: acetonitrile
Matrix: air
Detection limit: 0.8 ug/sample.

Method: EPA-RCA 5030C
Procedure: purge and trap
Analyte: acetonitrile
Matrix: water
Detection Limit: not provided.

Method: EPA-RCA 8015C
Procedure: gas chromatography with flame ionization detector
Analyte: acetonitrile
Matrix: surface water, ground water, and solid matrices
Detection Limit: 6 ug/L.

Method: EPA-RCA 8033
Procedure: gas chromatography with nitrogen-phosphorus detection
Analyte: acetonitrile
Matrix: water
Detection Limit: 1.7 ug/L.

Clinical Laboratory Methods of Acetonitrile:
Simple & rapid head space MS screening technique for volatiles in blood & postmortem tissue is described.
Acetonitrile in blood-enriched specimens exhibited characteristic mass spectra.

Volatile substance can be separated from biological liquids after injection onto packed gas-chromatographic columns or in a closed vessel or by controlled temp diffusion from liq phase into air above sample (head space).
Separated volatile component including acetonitrile may be identified by GC.

Handling and Storage of Acetonitrile:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling the product must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Acetonitrile without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Safe Storage:
Fireproof.
Keep in a well-ventilated room.
Separated from acids, bases, strong oxidants and food and feedstuffs.

Storage Conditions:
Protect containers against physical damage.
Outdoor or detached storage is preferable.

Separate from any sources of ignition and combustible materials.
Storage room should be well-ventilated.

Inside storage should be in a standard flammable liquids storage warehouse, room, or cabinet.
Separate from oxidizing materials. Outside or detached storage is preferred.

Store in tightly closed containers in a cool, well ventialted area.
Metal containers involving the transfer of this chemical should be grounded and bonded.

Where possible, automatically pump liquid from drums or other storage containers to process containers.
Drums must be equipped with self-closing valves, pressure vacuum bungs; and flame arresters.
Use only non-sparking tools and equipment, especially when opening and closing containers of this chemical.

First Aid Measures of Acetonitrile:

EYES:
First check the victim for contact lenses and remove if present.
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.

Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

SKIN:
IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing.
Gently wash all affected skin areas thoroughly with soap and water.
If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.

INHALATION:
IMMEDIATELY leave the contaminated area.
Take deep breaths of fresh air.

If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital.
Provide proper respiratory protection to rescuers entering an unknown atmosphere.

Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used.
If not available, use a level of protection greater than or equal to that advised under Protective Clothing.

INGESTION:
DO NOT INDUCE VOMITING.
Volatile chemicals have a high risk of being aspirated into the victim's lungs during vomiting which increases the medical problems.

If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center.
IMMEDIATELY transport the victim to a hospital.

If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body.
DO NOT INDUCE VOMITING.
IMMEDIATELY transport the victim to a hospital.

Fire Fighting of Acetonitrile:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

For fire involving UN1170, UN1987 or UN3475, alcohol-resistant foam should be used.

Ethanol (UN1170) can burn with an invisible flame.
Use an alternate method of detection (thermal camera, broom handle, etc.).

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto the product.
If Acetonitrile can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

For massive fire, use unmanned master stream devices or monitor nozzles.
If this is impossible, withdraw from area and let fire burn.

Accidental Release Measures of Acetonitrile:

Isolation and Evacuation:
Isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions.
Also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Identifiers of Acetonitrile:
CAS Number: 75-05-8
Beilstein Reference: 741857
ChEBI: CHEBI:38472
ChEMBL: ChEMBL45211
ChemSpider: 6102
ECHA InfoCard: 100.000.760
EC Number: 200-835-2
Gmelin Reference: 895
MeSH: acetonitrile
PubChem CID: 6342
RTECS number: AL7700000
UNII: Z072SB282N
UN number: 1648
CompTox Dashboard (EPA): : DTXSID7020009
InChI: InChI=1S/C2H3N/c1-2-3/h1H3
Key: WEVYAHXRMPXWCK-UHFFFAOYSA-N
SMILES: CC#N

Substance name: acetonitrile
Trade name: Acetonitrile
EC no: 200-835-2
CAS no: 75-05-8
HS code: 29269095
Formula: C2H3N

CAS number: 75-05-8
EC index number: 608-001-00-3
EC number: 200-835-2
Grade: Reag. Ph Eur
Hill Formula: C₂H₃N
Chemical formula: CH₃CN
Molar Mass: 41.05 g/mol
HS Code: 2926 90 70

Synonym(s): ACN, Cyanomethane, Ethyl nitrile, Methyl cyanide
Linear Formula: CH3CN
CAS Number: 75-05-8
Molecular Weight: 41.05
Beilstein: 741857
EC Number: 200-835-2
MDL number: MFCD00001878
eCl@ss: 39031501
PubChem Substance ID: 57648217
NACRES: NA.21

Typical Properties of Acetonitrile:
Chemical formula: C2H3N
Molar mass: 41.053 g·mol−1
Appearance: Colorless liquid
Odor: Faint, distinct, fruity
Density: 0.786 g/cm3 at 25°C
Melting point: −46 to −44 °C; −51 to −47 °F; 227 to 229 K
Boiling point: 81.3 to 82.1 °C; 178.2 to 179.7 °F; 354.4 to 355.2 K
Solubility in water: Miscible
log P: −0.334
Vapor pressure: 9.71 kPa (at 20.0 °C)
Henry's law constant (kH): 530 μmol/(Pa·kg)
Acidity (pKa): 25
UV-vis (λmax): 195 nm
Absorbance: ≤0.10
Magnetic susceptibility (χ): −28.0×10−6 cm3/mol
Refractive index (nD): 1.344

Quality Level: 200
Vapor density: 1.41 (vs air)
Vapor pressure: 72.8 mmHg ( 20 °C)
Assay: 99.8%
Form: liquid
Autoignition temp.: 973 °F
Expl. lim.: 16 %
Technique(s): solid phase extraction (SPE): suitable
Impurities:
<0.001% water
<0.005% water (100 mL pkg)
Evapn. residue: <0.0005%
Color: colorless
Refractive index: n20/D 1.344 (lit.)
bp: 81-82 °C (lit.)
mp: −45 °C (lit.)
Solubility: water: soluble (completely)
Density: 0.786 g/mL at 25 °C (lit.)
SMILES string: CC#N
InChI: 1S/C2H3N/c1-2-3/h1H3
InChI key: WEVYAHXRMPXWCK-UHFFFAOYSA-N

Boiling point: 81.6 °C (1013 hPa)
Density: 0.78 g/cm3 (20 °C)
Explosion limit: 3.0 - 17 %(V)
Flash point: 2 °C
Ignition temperature: 524 °C
Melting Point: -45.7 °C
Vapor pressure: 98.64 hPa (20 °C)

Molecular Weight: 41.05
XLogP3-AA: 0
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 41.026549100
Monoisotopic Mass: 41.026549100
Topological Polar Surface Area: 23.8 Ų
Heavy Atom Count: 3
Complexity: 29.3
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Acetonitrile:
Purity (GC): ≥ 99.9 %
Identity (IR): conforms
Evaporation residue: ≤ 2.0 mg/l
Water: ≤ 0.02 %
Color: ≤ 10 Hazen
Density (d 20 °C/20 °C): 0.78
Refractive index (n 20/D): 1.344
Boiling range (80-82°C): ≥ 95 % (v/v)
Acidity: ≤ 0.0002 meq/g
Alkalinity: ≤ 0.0002 meq/g
Gradient grade (at 210 nm): ≤ 1.0 mAU
Gradient grade (at 254 nm): ≤ 0.5 mAU
Fluorescence (as quinine at 254 nm): ≤ 1.0 ppb
Fluorescence (as quinine at 365 nm): ≤ 0.5 ppb
Transmission (at 193 nm): ≥ 60 %
Transmission (at 195 nm): ≥ 80 %
Transmission (from 230 nm): ≥ 98 %

Thermochemistry of Acetonitrile:
Heat capacity (C): 91.69 J/(K·mol)
Std molar entropy (S⦵298): 149.62 J/(K·mol)
Std enthalpy of formation (ΔfH⦵298): 40.16–40.96 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): −1256.03 – −1256.63 kJ/mol

Related compounds of Acetonitrile:

Related alkanenitriles:
Hydrogen cyanide
Thiocyanic acid
Cyanogen iodide
Cyanogen bromide
Cyanogen chloride
Cyanogen fluoride
Aminoacetonitrile
Glycolonitrile
Cyanogen
Propionitrile
Aminopropionitrile
Malononitrile
Pivalonitrile
Acetone cyanohydrin
DBNPA

Names of Acetonitrile:

Regulatory process names:
Acetonitril
Acetonitrile
ACETONITRILE
Acetonitrile
acetonitrile
acetonitrile; cyanomethane
Cyanomethane
cyanomethane
Cyanure de methyl
Ethanenitrile
Ethyl nitrile
Methane, cyano-
Methanecarbonitrile
Methyl cyanide
Methylkyanid

Translated names:
acetonitril (cs)
acetonitril (da)
Acetonitril (de)
acetonitril (hr)
acetonitril (hu)
acetonitril (nl)
acetonitril (no)
acetonitril (ro)
acetonitril (sk)
acetonitril (sl)
acetonitril (sv)
acetonitrilas (lt)
acetonitrile (it)
acetonitrilo (es)
acetonitrilo (pt)
acetonitrils (lv)
acetonitryl (pl)
acétonitrile; cyanométhane (fr)
Asetonitriili (fi)
Atsetonitriil (et)
cianeto de metilo (pt)
cianometan (hr)
cianometan (ro)
cianometan (sl)
cianometanas (lt)
cianometán (hu)
cianometāns (lv)
cianuro de metilo (es)
Cyanomethane (de)
cyanométhane (fr)
cyanure de méthyle (fr)
cyjanek metylu (pl)
kyanometán (sk)
methylkyanid (cs)
nitryl kwasu octowego (pl)
Syaanimetaani (fi)
Tsüanometaan (et)
ακετονιτρίλιο (el)
ацетонитрил (bg)
цианометан (bg)

CAS names:
Acetonitrile

IUPAC names:
Acetonitril
acetonitril
Acetonitril
ACETONITRILE
Acetonitrile
acetonitrile
ACETONITRILE
Acetonitrile
acetonitrile
Acetonitrile IMDG OR
acetonitrile-
acetonitrile; cyanomethane
Acetonitrile
Acetronitrile
Acetronitrile
Actonitrile
AKS-12
cianuro de metilo
cyanomethane
Cyanure de méthyle
etanonitrile
ethanenitrile
Methyl cyanide
Methyl cyanide, Acetonitrile, Ethyl nitrile, Cyanomethane, ACN

Preferred IUPAC name:
Acetonitrile

Systematic IUPAC name:
Ethanenitrile

Trade names:
ACETONITRILE
Acetonitrile
acetonitrile
Acetonitrile technical

Other names:
Cyanomethane
Ethyl nitrile
Methanecarbonitrile
Methyl cyanide
MeCN
ACN

Synonyms of Acetonitrile:
ACETONITRILE
Cyanomethane
Methyl cyanide
75-05-8
Ethanenitrile
Ethyl nitrile
Methanecarbonitrile
Methane, cyano-
Acetonitril
Cyanure de methyl
Methylkyanid
MeCN
Methylkyanid [Czech]
USAF EK-488
RCRA waste number U003
NCI-C60822
Cyanure de methyl [French]
Acetonitril [German, Dutch]
Acetonitrile, anhydrous
CH3CN
NCMe
Acetonitrile, dimer
148642-19-7
Acetonitrile with 0.1% ammonium acetate
CH3-C#N
CHEBI:38472
Z072SB282N
NSC-7593
ACETONITRILE WITH 0.1per cent AMMONIUM ACETATE
MFCD00001878
Acetonitrile [UN1648] [Flammable liquid]
Acetonitril (GERMAN, DUTCH)
Acetonitrile, for DNA synthesis
acetnitrile
Ethanonitrile
66016-35-1
CCN
HSDB 42
CCRIS 1628
NSC 7593
Acetonitrile, for HPLC, gradient grade, >=99.9%
EINECS 200-835-2
UN1648
RCRA waste no. U003
acetonitile
acetonitnle
acetonitriie
acteonitril
acteonitrile
actonitrile
methylcyanide
methylnitrile
ace-tonitrile
aceto-nitrile
acetonitrile-
UNII-Z072SB282N
AI3-00327
Acetonitrile ACS
CC.equiv.N
Acetonitrile LC-MS
Cyanomethylidyne radical
Acetonitrile HPLC grade
H3CCN
ACETONITRILE [II]
ACETONITRILE [MI]
Acetonitrile, LCMS grade
bmse000826
bmse000896
ACETONITRILE [HSDB]
EC 200-835-2
Acetonitrile, HPLC Reagent
WLN: NC1
Acetonitrile, >=99.5%
ACETONITRILE [MART.]
Acetonitrile with formic acid
ACETONITRILE [USP-RS]
Acetonitrile, puriss., 95%
CHEMBL45211
Acetonitrile, for chromatography
DTXSID7020009
Acetonitrile UV/HPLC ACS grade
Acetonitrile, analytical standard
Acetonitrile for preparative HPLC
Acetonitrile, AR, >=99.5%
Acetonitrile, Environmental Grade
NSC7593
Acetonitrile, anhydrous, 99.8%
Acetonitrile, >=99.5% (GC)
Acetonitrile, HPLC gradient Grade
STR02933
Acetonitrile, far UV/gradient grade
Tox21_202481
Acetonitrile, HPLC Grade (Far UV)
Acetonitrile, p.a., dry, 99.9%
Acetonitrile, ReagentPlus(R), 99%
c1151
STL283937
Acetonitrile, Spectrophotometric Grade
Acetonitrile, >=99.8%, for HPLC
Acetonitrile, for HPLC, >=99.9%
AKOS000269067
Acetonitrile, HPLC Plus, >=99.9%
NA 1648
UN 1648
Acetonitrile, >=99.5%, ACS reagent
Acetonitrile, ACS reagent, >=99.5%
Acetonitrile, AldraSORB(TM), 99.8%
Acetonitrile, purum, >=99.0% (GC)
CAS-75-05-8
Acetonitrile (for HPLC) isocratic grade
Acetonitrile, HPLC grade, >=99.93%
NCGC00091552-01
NCGC00260030-01
Acetonitrile 1000 microg/mL in Methanol
Acetonitrile, purification grade, 99.8%
Ultrapure Acetonitrile, for DNA synthesis
Acetonitrile with 0.1% Formic Acid (v/v)
Acetonitrile, biotech. grade, >=99.93%
Acetonitrile, p.a., ACS reagent, 99.8%
Acetonitrile, SAJ first grade, >=99.0%
A0060
A0293
A0793
Acetonitrile, JIS special grade, >=99.5%
FT-0621807
FT-0621808
Acetonitrile, anhydrous, ZerO2(TM), 99.8%
EN300-21632
Acetonitrile, for HPLC-GC, >=99.8% (GC)
Acetonitrile, for UHPLC, for mass spectrometry
Acetonitrile, Supergradient HPLC Grade (Far UV)
Acetonitrile, spectrophotometric grade, >=99.5%
Q408047
Acetonitrile, for HPLC, for UV, >=99.9% (GC)
Acetonitrile, puriss. p.a., ACS reagent, 99.8%
J-008497
Acetonitrile, for preparative HPLC, >=99.8% (GC)
Acetonitrile, for synthesis of DNA, >=99.9% (GC)
Acetonitrile, electronic grade, 99.999% trace metals basis
Acetonitrile, for HPLC, gradient grade, >=99.9% (GC)
Acetonitrile, for HPLC, gradient grade, >=99.90% (GC)
Acetonitrile, puriss. p.a., ACS reagent, >=99.5% (GC)
Acetonitrile with 0.1% ammonium acetate, tested for UHPLC-MS
Acetonitrile, for protein sequence analysis, >=99.8% (GC)
Acetonitrile, Vetec(TM) reagent grade, anhydrous, >=99.8%
Acetonitrile, Preparateur, >=99.9% (GC), Customized plastic drum
Acetonitrile, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.5% (GC)
Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material
Acetonitrile, Preparateur, >=99.9% (GC), One-time steel-plastic (SP) drum
Alcohol Determination - Acetonitrile, United States Pharmacopeia (USP) Reference Standard
Residual Solvent - Acetonitrile, Pharmaceutical Secondary Standard; Certified Reference Material
Residual Solvent Class 2 - Acetonitrile, United States Pharmacopeia (USP) Reference Standard
200-664-3 [EINECS]
200-835-2 [EINECS]
232-148-9 [EINECS]
741857 [Beilstein]
75-05-8 [RN]
Acetonitril [Dutch] [ACD/IUPAC Name]
Acetonitril [German] [ACD/IUPAC Name]
Acetonitrile [ACD/Index Name] [ACD/IUPAC Name] [Wiki]
Acetonitrile [Italian] [ACD/Index Name] [ACD/IUPAC Name]
Acétonitrile [French] [ACD/IUPAC Name]
Acetonitrile ZerO2(R)
Acetonitrilo [Spanish]
Alcohol Determination - Acetonitrile
Amidite Diluent
Asetonitril [Turkish]
cianometano [Italian]
cianuro di metile [Italian]
cyanomethane
Cyanure de methyl [French]
Degassed and low oxygen acetonitrile
etanonitrile
Ethane nitrile
Ethanenitrile [Wiki]
ethanonitrile
Ethyl nitrile
MeCN [Formula]
Methane, cyano-
methyl cyanide
Methylidyne, cyano-
Methylkyanid [Czech]
MFCD00001878 [MDL number]
NC1 [WLN]
NCMe [Formula]
Residual Solvent - Acetonitrile
Residual Solvent Class 2 - Acetonitrile
Ацетонитрил [Russian]
18605-40-8 [RN]
1-Aminoethane
Acetonitrile ACS
Acetonitrile EMPROVE(R) ESSENTIAL
Acetonitrile LC-MS
Acetonitrile Non UV
Acetonitrile withmissing
Acetonitrile, anhydrous
Acetonitrile, GlenDry, anhydrous
Acetonitrile, Hp
Acetonitrile/Formic Acidmissing
Acetonitrile/TFAmissing
Acetonitrilemissing
ACN + TFA
methanecarbonitrile
Methyl Cyanide, Ethanenitrile
ACETYL TRIBUTYL CITRATE
Acetyl Tributyl Citrate Acetyl tributyl citrate is an organic compound that is used as a plasticizer. As such, it is a potential replacement of DEHP and DINP.[1] It is a colorless liquid that is soluble in organic solvents. Acetyl tributyl citrate is found in nail polish and other cosmetics. Acetyl tributyl citrate is prepared by acetylation of tributylcitrate. Acetyl tributyl citrate is an indirect food additive for use only as a component of adhesives. Prior-sanctioned food ingredients. Substances classified as plasticizers, when migrating from food packaging material. Acetyl tributyl citrate is included on this list. The metabolism of acetyl tributyl citrate was evaluated using groups of male rats (number of animals, weights, and strain not stated). Each animal received a single oral dose of 14C-acetyl tributyl citrate (dose not stated). At 48 hr post dosing, approximately 99% of the administered dose had been excreted either in urine (59% to 70%), feces (25% to 36%), or in the expired air (2%). Only 0.36% to 1.26% of the dose remained in the tissues or carcass. The metabolism of acetyl tributyl citrate was evaluated using groups of male rats (number of animals, weights, and strain not stated). ... Both the absorption and metabolism of 14C-Acetyl tributyl Citrate proceeded rapidly, and the following metabolites were identified: acetyl citrate, monobutyl citrate, acetyl monobutyl citrate, dibutyl citrate, and acetyl dibutyl citrate. IDENTIFICATION: Acetyl tributyl citrate is a colorless liquid. It has a very faint sweet, herb-like odor and a mild fruity taste. Acetyl tributyl citrate has moderate solubility in water. USE: Acetyl tributyl citrate is an important commercial chemical that is used as a solvent in paints, inks, and nail enamel. It is also used to make plastics more flexible, including plastics used to make toys and food wrappings. Acetyl tributyl citrate is added as a flavor ingredient in non-alcoholic beverages and is used in the manufacture of many pharmaceutical drugs. EXPOSURE: Workers that use or produce acetyl tributyl citrate may breathe in mists or have direct skin contact. The general population may be exposed to small amounts by drinking beverages containing acetyl tributyl citrate, eating foods stored in plastic materials containing acetyl tributyl citrate, or from skin contact with products containing acetyl tributyl citrate. If acetyl tributyl citrate is released to air, it will be broken down by reaction with other chemicals. It will be in or on particles that eventually fall to the ground. If released to water or soil, acetyl tributyl citrate is expected to bind to soil particles or suspended particles. Acetyl tributyl citrate is not expected to move through soil. Acetyl tributyl citrate is expected to move into air from wet soils or water surfaces. However, binding to soil may slow down this process. Acetyl tributyl citrate is expected to be broken down by microorganisms and may have moderate build up in tissues of aquatic organisms. RISK: Acetyl tributyl citrate did not cause skin irritation or allergic reactions in human volunteers. Additional information about the potential for acetyl tributyl citrate to produce toxic effects in humans was not located. Very mild to no skin irritation and moderate eye irritation have been reported in laboratory animals. No toxic effects were observed in laboratory animals given a single high oral dose of acetyl tributyl citrate. Diarrhea, weight loss, and liver damage were observed in laboratory animals repeatedly fed very high doses. Body weight loss was observed in laboratory animals following repeated skin application of high levels of acetyl tributyl citrate. No changes were observed in reproduction or development in rats exposed to high dose over a short period of time. No tumors were reported in laboratory animals following life-time exposure to high dietary levels of acetyl tributyl citrate. The potential for acetyl tributyl citrate to cause cancer in humans has not been assessed by the U.S. EPA IRIS program, the International Agency for Research on Cancer, or the U.S. National Toxicology Program 13th Report on Carcinogens. Acetyl tributyl citrate (ATBC) is a colorless liquid. It is the most widely used phthalate substitute plasticizer. Acetyl tributyl citrate is used in products such as food wrap, vinyl toys, and pharmaceutical excipients. Acetyl tributyl citrate is also used as a flavor ingredient in non-alcoholic beverages. HUMAN EXPOSURE AND TOXICIY: The skin irritation potential of acetyl tributyl citrate was evaluated using 59 men and women, all of whom had history of diabetes, psoriasis, or active dermatoses. Acetyl tributyl citrate was nonirritating to the skin, and reactions suggestive of contact sensitization were not observed during the study. In vitro Acetyl tributyl citrate increased CYP3A4 messenger RNA (mRNA) levels and enzyme activity in the human intestinal cells but not in human liver cells. ANIMAL STUDIES: Acute oral toxicity of Acetyl tributyl citrate in cats and rats is low. CYP3A1 mRNA levels were increased in the intestine but not the liver of ATBC-treated rats. In a 90-day repeated-dose oral dietary study in rats, decreased body weight and organ weight changes were observed at 1000 mg/kg-bw/day. In a combined repeated dose/reproductive/ developmental toxicity study in rats, organ weight and histopathological changes were observed in adults at 1000 mg/kg-bw/day. In a 2-generation reproductive toxicity study in rats, reduced body weight was observed in F1 males at 300 mg/kg-bw/day. In the same study, no other treatment related effects were observed. In the combined repeated dose/ reproductive/ developmental toxicity study in rats previously described, histopathological changes were observed in the liver of adult males at 300 mg/kg-bw/day. In the same study, decreased litter size and decreased number of implantations were observed at 1000 mg/kg-bw/day. Acetyl tributyl citrate did not induce gene mutations in bacteria or mammalian cells in vitro and did not induce chromosomal aberrations in mammalian cells in vitro. ECOTOXICITY STUDIES: For acetyl tributyl citrate, the 96-hr LC50 values for fish range from 38 to 60 mg/L, the 48-hr EC50 value for aquatic invertebrates is 7.8 mg/L and the 72-hr EC50 values for aquatic plants are 11.5 mg/L for biomass and 74.4mg/L for growth rate, respectively. Application Acetyl tributyl citrate (TBoAC) can be used: • As a plasticizer to improve flexibility and impact properties of polylactide (PLA) polymer.[1] • As a processing additive for the formulation of bulk heterojunction (BHJ) polymeric organic solar cells (OSCs) to improve their efficiency.[2] • In the preparation of semiconducting biopolymer composites of poly(3-hydroxy butyrate) (PHB).[3] • In the synthesis of functionalized poly(vinyl chloride)(PVC) membranes for selective separation of perchlorate from water. The skin irritation potential of acetyl tributyl citrate was evaluated using 59 men and women (age range = 21-60 years), all of whom had history of diabetes, psoriasis, or active dermatoses. ... Occlusive patches moistened with 0.4 mL of acetyl tributyl citrate were applied to the upper arm of each subject on Mondays, Wednesdays, and Fridays for 3 consecutive weeks. Each patch was removed 24 hours post application. Induction reactions were scored prior to patch applications (second through ninth visits) and at the time of the tenth visit. Duplicate challenge of the test material was made after a two-week non-treatment period. ... One challenge patch was applied to the original test site, and , another, to an adjacent site. Challenge reactions were scored at 48 and 96 hours post application. /Acetyl tributyl citrate/ was nonirritating to the skin, and reactions suggestive of contact sensitization were not observed during the study. The in vitro cytotoxicity of acetyl tributyl citrate in HeLa cell cultures (human cell line) was evaluated using the metabolic inhibition test, supplemented by microscopy of cells after 24 hours of incubation (the MIT-24 test system). ... After 24 hours, cell viability was determined by microscopy. Two endpoints of cytoinhibition (total and partial inhibition) were estimated after 24 hours, based on the absence or scarcity of spindle-shaped cells, and, after 7 days.... The following values for minimal inhibitory concentration were reported for acetyl tributyl citrate: 13 mg/mL (for total inhibition at 24 hours), 3.8 mg/mL (for partial inhibition at 24 hours), and 5.7 mg/mL (for total and partial inhibition at 7 days). Acetyl tributyl citrate caused little toxicity in HeLa cell cultures. The effects of polyvinyl-chloride (PVC) tubing extracts were investigated in isolated ileum of guinea-pigs. Ileum were isolated and mounted in tissue baths. Tubing ingredients from PVC or tubing extracts of the plasticizer acetyl-N-tributyl-citrate (Acetyl tributyl citrate) were added to the bath for 15 minutes. Contractions or modifications of methacholine responses were measured. ...A significant and characteristic effect was seen for Acetyl tributyl citrate in ileum, consisting of rapid contractions and relaxations which were dependent on concentrations. The spasms were unaffected by tetrodotoxin. No spasmogenic effect was seen for Acetyl tributyl citrate in human small intestine or colon. None of the other tubing ingredients had any spasmogenic action, including PVC extracts. No methacholine contractions occurred with the other ingredients. Tubing extracts containing Acetyl tributyl citrate produced spasms similar to chemical Acetyl tributyl citrate. Steroid and xenobiotic receptor (SXR) is activated by endogenous and exogenous chemicals including steroids, bile acids, and prescription drugs. SXR is highly expressed in the liver and intestine, where it regulates cytochrome P450 3A4 (CYP3A4), which in turn controls xenobiotic and endogenous steroid hormone metabolism. However, it is unclear whether Food and Drug Administration (FDA)-approved plasticizers exert such activity. ...We found that four of eight FDA-approved plasticizers increased SXR-mediated transcription. In particular, acetyl tributyl citrate (ATBC), an industrial plasticizer widely used in products such as food wrap, vinyl toys, and pharmaceutical excipients, strongly activated human and rat SXR. Acetyl tributyl citrate increased CYP3A4 messenger RNA (mRNA) levels and enzyme activity in the human intestinal cells but not in human liver cells. Acute Exposure/ The acute oral toxicity of Acetyl tributyl citrate was evaluated using five rats (strain and weight not stated). The test substance was administered at doses ranging from 10 to 30 mL/kg, and animals were observed for 3 weeks. Signs of systemic toxicity were not observed, and none of the animals died. A single dose of acetyl tributyl citrate (30 to 50 mL/kg) was administered by stomach tube to each of four fasted cats (weights not stated), and animals were observed for 2 months. Two additional cats served as controls. Signs of nausea were observed in test animals, and, within a few hours of dosing, diarrhea (oozing of oily material) was noted. The diarrhea subsided within 24 hours of dosing. The behavior and general appearance of animals indicated systemic toxicity. Two cats dosed with 50 mL/kg were used for hematological evaluations and no effects on the following blood parameters were found: blood cell counts, hemoglobin, sugar, nonprotein nitrogen, or creatinine. Results from urinalyses indicate no abnormalities in specific gravity, albumin, sugar, pH, or microscopic formed elements. Acetyl tributyl citrate is not reported as found in nature. Acetyl tributyl citrate's production and use as a plasticizer for vinyl and other resin(1,2), as a solvent and functional fluid in adhesives, paints, coating and inks(2) as a flavor ingredient(3) and in nail enamel(4) may result in its release to the environment through various waste streams(SRC). Based on a classification scheme(1), an estimated Koc value of 3280(SRC), determined from a log Kow of 4.90(2) and a regression-derived equation(3), indicates that acetyl tributyl citrate is expected to have slight mobility in soil(SRC). Volatilization of acetyl tributyl citrate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.2X10-5 atm-cu m/mole(SRC), derived from its estimated vapor pressure, 3X10-4 mm Hg(3), and water solubility, 5 mg/L(4). However, adsorption to soil is expected to attenuate volatilization(SRC). Acetyl tributyl citrate is not expected to volatilize from dry soil surfaces(SRC) based upon its estimated vapor pressure of 3X10-4 mm Hg at 25 °C(SRC), determined from a fragment constant method(3). An 82% of theoretical BOD using activated sludge in the Japanese MITI test(5) suggests that biodegradation is an important environmental fate process in soil(SRC). Acetyl tributyl citrate was shown to biodegrade extensively in several other biodegradation studies and simulation tests(6,7). Two soil degradation studies observed rapid biomineralization of acetyl tributyl citrate(7). What Is It? Acetyl Triethyl Citrate, Acetyl Tributyl Citrate, Acetyl Trihexyl Citrate and Acetyl Triethylhexyl Citrate are a clear oily liquids with essentially no odor. In cosmetics and personal care products, Acetyl Triethyl Citrate and Acetyl Tributyl Citrate are used mainly in the formulation of nail care products. Acetyl Tributyl Citrate may also be found in eye makeup. Why is it used in cosmetics and personal care products? Acetyl Triethyl Citrate, Acetyl Tributyl Citrate, Acetyl Trihexyl Citrate and Acetyl Triethylhexyl Citrate may be used as plasticizers for film-forming ingredients. Acetyl Trihexyl Citrate and Acetyl Triethylhexyl Citrate may also be used as skin conditioning agents - emollients. Acetyl Triethyl Citrate, Acetyl Tributyl Citrate, Acetyl Trihexyl Citrate and Acetyl Triethylhexyl Citrate are esters of citric acid. Citric acid may be obtained from natural sources such as citrus fruits. According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), acetyl tributyl citrate, which has an estimated vapor pressure of 3X10-4 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase acetyl tributyl citrate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 27 hours(SRC), calculated from its rate constant of 1.4X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(2). Particulate-phase acetyl tributyl citrate may be removed from the air by wet and dry deposition(SRC). Acetyl tributyl citrate, present at an initial concentration of 30 mg/L, reached 82% of the theoretical BOD in 4 weeks with an activated sludge inoculum at 100 mg/L in the modified MITI test which classified the compound as readily biodegradable(1). Acetyl tributyl citrate was shown to biodegrade extensively in several other biodegradation studies and simulation tests(2,3). In a sewage column degradation test using acclimated sludge, acetyl tributyl citrate biodegraded >90% in hours(3). An aerobic biodegradation test in soil using a static biometer system found acetyl tributyl citrate to be readily biodegradable with theoretical CO2 evolution of 72.9% to >100% (as various concentrations) over 42 days of incubation(3). A 52-day aerobic study in soil observed rapid biodegradation with mineralization (ThCO2) of 83 to >100% over 52 days(3). The rate constant for the vapor-phase reaction of acetyl tributyl citrate with photochemically-produced hydroxyl radicals has been estimated as 1.4X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 27 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). A base-catalyzed second-order hydrolysis rate constant of 5.8X10-2 L/mole-sec(SRC) was estimated using a structure estimation method(1); this corresponds to half-lives of 3.8 years and 140 days at pH values of 7 and 8, respectively(1). An estimated BCF of 35 was calculated in fish for acetyl tributyl citrate(SRC), using a log Kow of 4.92(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC), provided the compound is not metabolized by the organism(SRC). The Koc of acetyl tributyl citrate is estimated as 3280(SRC), using a log Kow of 4.92(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that acetyl tributyl citrate is expected to have slight mobility in soil. The Henry's Law constant for acetyl tributyl citrate is estimated as 3.2X10-5 atm-cu m/mole(SRC) derived from its estimated vapor pressure, 3.0X10-4 mm Hg(1), and water solubility, 5 mg/L(2). This Henry's Law constant indicates that acetyl tributyl citrate is expected to volatilize from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 2.6 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 25 days(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 335 days if adsorption is considered(4). Acetyl tributyl citrate's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur, but the rate may be attenuated by adsorption to soil(SRC). Acetyl tributyl citrate is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1). Acetyl tributyl citrate was identified in 2 water samples taken from the River Lee, Great Britain at trace levels(1). Acetyl tributyl citrate is reportedly used as a flavor ingredient in nonalcoholic beverages at a concentration of 1.0 ppm(1). A monitoring study of hospital diets in Japan for plasticizers in hospital food detected acetyl tributyl citrate at levels (in one hospital) that corresponded to a daily intake of 1228 ug/day(2); the source of the acetyl tributyl citrate in the food was suspected to be cling-film wrapping or other packaging(2). Monitoring tests determined that acetyl tributyl citrate plasticizer in plastic films migrated from the film into cooked poultry meat during microwave cooking(3). Food-grade polyvinyl chloride (PVC) cling-film containing 5.3% (w/w) di(2-ethylhexyl) adipate (DEHA) and 3.0% (w/w) acetyl tributyl citrate (ATC) plasticizers was used to wrap halawa tehineh (halva) samples. Samples were split into two groups and stored at 25+/-1 degrees C. One group was analyzed for DEHA and Acetyl tributyl citrate content at intervals between 0.5 and 240hr of contact (kinetic study) and a second group was cut into slices (1.5mm thick) after 240hr of halva/PVC contact and was analyzed for DEHA and Acetyl tributyl citrate content (penetration study). Determination of both plasticizers was performed using a direct gas chromatographic (GC) method after extraction of DEHA from halva samples. DEHA readily migrated into halva samples: the equilibrium amount of DEHA in halva (3.31mg/sq dm film or 81.4mg/kg halva) corresponding to a loss of 54.7% (w/w) DEHA from PVC film. This value is slightly higher than the limit of 3mg/ sq dm of film surface set by the European Union for DEHA. The equilibrium amount of Acetyl tributyl citrate in halva was 1.46mg/sq dm (36.1mg/kg) corresponding to a loss of 42.7% Acetyl tributyl citrate from PVC film. With regard to the penetration of both placticizers into halva samples, migration of DEHA was detectable up to the 7th slice beneath the surface of halva (total depth 10.5mm) while the migration of Acetyl tributyl citrate was detectable up to the 5th slice (total depth 7.5mm). According to the 2012 TSCA Inventory Update Reporting data, 6 reporting facilities estimate the number of persons reasonably likely to be exposed in their respective industrial use in the United States manufacturing, processing, or use of acetyl tributyl citrate (77-90-7) may be as low as <10 workers up to the range of 50-99 workers per plant; the data may be greatly underestimated due to confidential business information (CBI) or unknown values(1). NIOSH (NOES Survey 1981-1983) has statistically estimated that 106,672 workers (98,182 of these are female) are potentially exposed to acetyl tributyl citrate in the US(1). Occupational exposure to acetyl tributyl citrate may occur through inhalation and dermal contact with this compound at workplaces where acetyl tributyl citrate is produced or used(SRC). Use data indicate that the general population may be exposed to acetyl tributyl citrate via inhalation of ambient air, ingestion of food containing this compound, and dermal contact with consumer products (such as cosmetics, paints and inks) containing acetyl tributyl citrate(SRC). About Acetyl tributyl citrate Helpful information Acetyl tributyl citrate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 per annum. Acetyl tributyl citrate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing. Consumer Uses Acetyl tributyl citrate is used in the following products: coating products, fillers, putties, plasters, modelling clay, finger paints, polishes and waxes, adhesives and sealants, metal surface treatment products, non-metal-surface treatment products, inks and toners, polymers, washing & cleaning products and cosmetics and personal care products. Other release to the environment of Acetyl tributyl citrate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives). Article service life Other release to the environment of Acetyl tributyl citrate is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints). Acetyl tributyl citrate can be found in complex articles, with no release intended: vehicles. Acetyl tributyl citrate can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), rubber (e.g. tyres, shoes, toys), paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), wood (e.g. floors, furniture, toys) and plastic used for articles with intense direct dermal (skin) contact during normal use (e.g. handles, ball pens). Widespread uses by professional workers Acetyl tributyl citrate is used in the following products: coating products, finger paints, metal surface treatment products, inks and toners, polymers, fillers, putties, plasters, modelling clay, non-metal-surface treatment products and washing & cleaning products. Acetyl tributyl citrate is used in the following areas: printing and recorded media reproduction and formulation of mixtures and/or re-packaging. Acetyl tributyl citrate is used for the manufacture of: plastic products. Other release to the environment of Acetyl tributyl citrate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use. Formulation or re-packing Acetyl tributyl citrate is used in the following products: polymers, washing & cleaning products, coating products, fillers, putties, plasters, modelling clay, finger paints, metal surface treatment products, non-metal-surface treatment products, inks and toners and cosmetics and personal care products. Release to the environment of Acetyl tributyl citrate can occur from industrial use: formulation of mixtures and formulation in materials. Uses at industrial sites Acetyl tributyl citrate is used in the following products: cosmetics and personal care products, pharmaceuticals, polymers, washing & cleaning products, adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, finger paints, metal surface treatment products, non-metal-surface treatment products, inks and toners, leather treatment products, lubricants and greases, paper chemicals and dyes, polishes and waxes and textile treatment products and dyes. Acetyl tributyl citrate is used in the following areas: formulation of mixtures and/or re-packaging, printing and recorded media reproduction and health services. Acetyl tributyl citrate is used for the manufacture of: plastic products, chemicals and food products. Release to the environment of Acetyl tributyl citrate can occur from industrial use: in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates), of substances in closed systems with minimal release, in processing aids at industrial sites, as processing aid, for thermoplastic manufacture and as processing aid. Manufacture Release to the environment of Acetyl tributyl citrate can occur from industrial use: manufacturing of the substance. Acetyl tributyl citrate's production and use as a plasticizer for vinyl and other resins, as a solvent and functional fluid in adhesives, paints, coating and inks and as a flavor ingredient may result in its release to the environment through various waste streams. If released to air, an estimated vapor pressure of 3X10-4 mm Hg at 25 °C indicates acetyl tributyl citrate will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase acetyl tributyl citrate will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 27 hours. Particulate-phase acetyl tributyl citrate will be removed from the atmosphere by wet and dry deposition. If released to soil, acetyl tributyl citrate is expected to have slight mobility based upon an estimated Koc of 3,280. Volatilization from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 3.2X10-5 atm-cu m/mole. However, adsorption to soil is expected to attenuate volatilization. Acetyl tributyl citrate is not expected to volatilize from dry soil surfaces based upon its estimated vapor pressure. Utilizing the Japanese MITI test, 82% of the Theoretical BOD was reached in 4 weeks indicating that biodegradation is an important environmental fate process in soil and water. Two soil degradation studies observed rapid biomineralization of acetyl tributyl citrate. If released into water, acetyl tributyl citrate is expected to adsorb to suspended solids and sediment based upon the estimated Koc. Acetyl tributyl citrate has been shown to biodegrade extensively in several other biodegradation studies and simulation tests. Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 2.6 and 25 days, respectively. However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 335 days if adsorption is considered. An estimated BCF of 35 suggests the potential for bioconcentration in aquatic organisms is moderate. Estimated hydrolysis half-lives of 3.8 years and 140 days were determined for pH 7 and 8, respectively. Occupational exposure to acetyl tributyl citrate may occur through inhalation and dermal contact with this compound at workplaces where acetyl tributyl citrate is produced or used. Use data indicate that the general population may be exposed to acetyl tributyl citrate via ingestion of food containing this compound, and dermal contact with consumer products (such as cosmetic, paints and inks) containing acetyl tributyl citrate.
ACETYLATED LANOLİ
Lanolin acetyl ester; Acetyl ester of lanolin; cas no: 61788-48-5
Acı Badem Ekstraktı
Prunus Amygdalus Dulcis Fruit Extract; almond fruit extract; prunus dulcis fruit extract; amygdalus communis linn. var. dulcis fruit extract cas no:90320-37-9
ACI BİBER AROMASI
hot pepper flavor; pepper flavor (hot)
ACID BLUE 80
Acid Blue 80 is an anthraquinone type water soluble organic dye.
Acid Blue 80 is likely used for coloration fabric & home care products and industrial & institutional cleaners, because its colour is stabile in wide range of pH (1-13).
Also used in cosmetics for wash down types with CI 61585 name.

CAS: 4474-24-2
MF: C32H31N2NaO8S2
MW: 658.72
EINECS: 224-748-4

Synonyms
4,4’-(1,4-anthraquinonylenediimino)di-2-mesitylenesulfonicacidisodiums;4,6-trimethyl-)bis(disodiumsalt;CI 61585;ACID BLUE 80;acid blue 80 (C.I. 61585);Acid Blue 80 (C.I.);sodium 3,3-(9,10-dioxoanthracene-1,4-diyldiimino)bis(2,4,6-trimethylbenzenesulphonate);Weakl Acid Brilliant ;Blue RAW;Acid blue 80;4474-24-2;C.I. ACID BLUE 80;Alizarine Fast Blue R;Alizarine Milling Blue R;Acid Brilliant Blue RAWL;Weak Acid Brilliant Blue RAW;Alizarine Blue BL;Acid Brilliant Blue Anthraquinone;Nylosan Blue C-L;Nylosan Blue F-L;Brilliant Alizarine Milling Blue BL;Acid Anthraquinone Brilliant Blue;Polar Brilliant Blue RAW;C.I. 61585;68214-05-1;Kislotnyi yarko-sinii antrakhinonovyi;ET8107F56D;Endanil Blue B;2-Mesitylenesulfonic acid, 4,4'-(1,4-anthraquinonylenediimino)di-, disodium salt;MFCD00001192;Sodium 3,3'-(9,10-dioxoanthracene-1,4-diyldiimino)bis(2,4,6-trimethylbenzenesulphonate);Benzenesulfonic acid, 3,3'-((9,10-dihydro-9,10-dioxo-1,4-anthracenediyl)diimino)bis(2,4,6-trimethyl-, disodium salt;Coomassie Blue B;disodium;3-[[9,10-dioxo-4-(2,4,6-trimethyl-3-sulfonatoanilino)anthracen-1-yl]amino]-2,4,6-trimethylbenzenesulfonate;C-WR Blue 10;Polar Brilliant Blue RAWL;Stenolana Brilliant Blue BL;Benzenesulfonic acid, 3,3'-((9,10-dihydro-9,10-dioxo-1,4-anthracenediyl)diimino)bis(2,4,6-trimethyl-, sodium salt (1:2);Atlantic Alizarine Milling Blue RB;EINECS 224-748-4;Lanasyn Blue F-L 150;NSC 295305;Anthraquinone Brilliant Blue;CI 61585;UNII-ET8107F56D;BLUE RAW;NAPHTHAZINE BLUE BL;ACID MILLING BLUE RAW;SCHEMBL341554;ACID BRILLIANT BLUE RAW;DTXSID2041705;UHXQPQCJDDSMCB-UHFFFAOYSA-L;BRILLIANT BLUE ANTHRAQUINONE;DIACID BRILLIANT SKY BLUE BW;Acid Blue 80, Dye content 40 %;WEAK ACID BRILLIANT BLUE RAWL;AKOS015903051;AKOS024319028;Benzenesulfonic acid, 3,3'-((9,10-dihydro-9,10-dioxo-1,4-anthracenediyl)diimino)bis(2,4- ,6-trimethyl-, disodium salt;Disodium 3,3'-((9,10-dihydro-9,10-dioxo-1,4-anthracenediyl)diimino)bis(2,4- ,6-trimethylbenzenesulfonate);J65.272E;FT-0621847;NS00013524;Q27277355;1,4-BIS((2,4,6-TRIMETHYL-3-(SODIOOXYSULFONYL)PHENYL)AMINO)ANTHRACENE-9,10-DIONE;3,3'-((9,10-DIHYDRO-9,10-DIOXOANTHRACENE-1,4-DIYL)BIS(IMINO))BIS(2,4,6-TRIMETHYLBENZENESULFONIC ACID SODIUM) SALT;3,3'-((9,10-DIHYDRO-9,10-DIOXOANTHRACENE-1,4-DIYL)BISIMINO)BIS(2,4,6-TRIMETHYLBENZENESULFONIC ACID SODIUM) SALT;3,3'-((9,10-DIHYDRO-9,10-DIOXOANTHRACENE-1,4-DIYL)DIIMINO)BIS(2,4,6-TRIMETHYLBENZENESULFONIC ACID SODIUM) SALT;3,3'-(9,10-DIHYDRO-9,10-DIOXOANTHRACENE-1,4-DIYLBIS(IMINO))BIS(2,4,6-TRIMETHYLBENZENESULFONIC ACID SODIUM) SALT;DISODIUM 3,3'-((9,10-DIHYDRO-9,10-DIOXO-1,4-ANTHRACENEDIYL)DIIMINO)BIS(2,4,6-TRIMETHYLBENZENESULFONATE);DISODIUM 3,3'-((9,10-DIOXO-9,10-DIHYDROANTHRACENE-1,4-DIYL)DIIMINO)BIS(2,4,6-TRIMETHYLBENZENESULFONATE);DISODIUM 3-((9,10-DIOXO-4-(2,4,6-TRIMETHYL-3-SULFONATOANILINO)ANTHRACEN-1-YL)AMINO)-2,4,6-TRIMETHYLBENZENESULFONATE;Sodium 3,3'-((9,10-dioxo-9,10-dihydroanthracene-1,4-diyl)bis(azanediyl))bis(2,4,6-trimethylbenzenesulfonate);sodium 3,3'-(9,10-dioxo-9,10-dihydroanthracene-1,4-diyl)bis(azanediyl)bis(2,4,6-trimethylbenzenesulfonate);Sodium3,3'-((9,10-dioxo-9,10-dihydroanthracene-1,4-diyl)bis(azanediyl))bis(2,4,6-trimethylbenzenesulfonate)

Acid Blue 80 Chemical Properties
Melting point: >300 °C(lit.)
Density: 1.537[at 20℃]
Colour Index: 61585
Water Solubility: 10.95g/L at 20℃
InChIKey: UHXQPQCJDDSMCB-UHFFFAOYSA-L
LogP :-1.304 at 20℃
EPA Substance Registry System: Acid Blue 80 (4474-24-2)

Acid Blue 80 is a dye & it gives coloration through solution.
For coloration this product, first pre-soluble in any suitable medium (like water or any convenient medium which is compatible to final product).
Acid Blue 80 is then used for the coloration of final product.
Acid Blue 80 is ideal for use in personal care applications.
Acid Blue 80 is a synthetic azo dye and belongs to the class of acid dyes.
Acid Blue 80 is also known as the Alizarine Cyanine Blue BWS or Acid Blue R.

Acid Blue 80 is often used as a textile dye, food dye, and in the paper industry.
The dye is commonly used in the production of denim, silk, wool, and synthetic fibers.
Acid Blue 80 has a wide range of industrial and scientific applications, and it is essential to understand its properties and characteristics to utilize it to its full potential.
Acid Blue 80 is relatively safe when used in scientific experiments.
However, Acid Blue 80's toxicity should be evaluated based on the specific experiment, and appropriate safety precautions should be taken to avoid exposure to the dye.

As Acid Blue 80 shows very good resistance to high pH it is widely used in the coloration of soap bars, but also suitable for shampoos, shower gels, etc.
Acid Blue 80's absorption maximum is between 580-590 nm depending on the pH.
Acid Blue 80 has excellent UV resistance.

Properties and Applications
Red light blue powder, soluble in water, but the solution for a long time have placed precipitation phenomenon.
The strong sulfuric acid dyes is red light blue, green light blue to dilute; In nitric acid are brown.
Water solution is deep blue, add hydrochloric acid or sodium hydroxide are in product blue.
Used for wool, silk, polyamide fiber and its blended fabric dyeing, dyeing scattered hair, tops, yarn packages, socks and knitting yarn and so on, also can be in wool and silk fabric printing directly, Acid Blue 80 can also be used in leather dyeing.

Acid blue 80 has a molecular formula of C20H13N2NaO5S and a CAS number of 12217-80-0.
The dye has an intense blue color, and Acid Blue 80 is soluble in water.
Acid blue 80 has a melting point of 142-144 °C and a boiling point of 614.5 °C.
The dye is stable under normal conditions, and Acid Blue 80 does not decompose easily.
Acid blue 80 has a low toxicity, and it is not considered harmful to humans or the environment.

Preparation
1,4-Dichloroanthracene-9,10-dione (1 Moore) or 1,4-Dihydroxyanthracene-9,10-dione (1 Moore) and 2,4,6-Trimethylbenzenamine(2 Moore) condensation, stlfonation, and translated into sodium salt.
Acid blue 80 is synthesized by diazotizing 4-nitro-o-toluidine and coupling it with 1-amino-4-nitronaphthalene-3,6-disulfonic acid.
The synthesized compound is purified using recrystallization and characterized using various techniques, including UV-visible spectroscopy, infrared spectroscopy, and mass spectrometry.

Analytical Methods
Acid blue 80 can be analyzed using various techniques, including high-performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC-MS), and UV-visible spectroscopy.
These techniques can determine the purity, stability, and degradation products of the dye.

Biological Properties
Acid blue 80 has low toxicity and is not considered harmful to humans or the environment.
However, Acid Blue 80 has been reported to cause skin irritation and allergic reactions in some individuals.
Acid blue 80 is also not biodegradable and can accumulate in the environment, leading to potential adverse effects on ecosystems.

Applications in Scientific Experiments
Acid blue 80 has several applications in scientific experiments, including the detection of proteins, DNA, and RNA.
The dye is also used as a staining agent in microscopy studies.
Acid blue 80 is essential in various analytical techniques, including HPLC, capillary electrophoresis, and gel electrophoresis.
ACRONAL S 790
ACRONAL S 790 is an aqueous styrene acrylic dispersion with medium viscosity and excellent pigment binding.

ACRONAL S 790 is an anionic medium viscosity dispersion with a small particle size.
ACRONAL S 790 has excellent compatibility with fillers and high pigment absorption.

Unpigmented ACRONAL S 790 films do not exhibit surface tack at room temperature.
They are transparent, elastic, glossy, highly resistant to moisture and dirt.
ACRONAL S 790 does not contain emulsifiers based on alkyl phenol ethoxylates.

ACRONAL S 790 is a standard, universal binder for sealants and primers applications.
ACRONAL S 790 shows a good filler compatibility and is compatible with many types of plasticizers.

ACRONAL S 790 is an aqueous dispersion of a styrene acrylic copolymer with medium viscosity and excellent pigment binding power.

ACRONAL S 790 is an APEO-free anionic styrene acrylic binder.
Has broad formulation latitude, medium viscosity and very good pigment binding capacity.

Offers exceptional cost performance and very good water resistance.
Exhibits outstanding saponification and alkaline resistance as well as superior dirt pick-up resistance.
ACRONAL S 790 is used in architectural finishes, interior paints, textured finishes, primers, exterior insulation and finishing systems (EIFS) as well as grouts.

ACRONAL S 790 acrylic dispersion is a styrene-acrylic dispersion (aqueous dispersion of an acrylic acid ester and styrene copolymer) for the manufacture of building paints (both exterior and interior), plasters and fillers, adhesives, used in the production of non-woven materials and textile coatings.

Application Area of ACRONAL S 790:
A feature of ACRONAL S 790 is its unique properties, thanks to which ACRONAL S 790 is used for the manufacture of building paints from high gloss to matt, which can be applied to plaster, masonry, asbestos cement, concrete, wood and other substrates both inside and outside the building.
In addition, having an extremely high pigment capacity on ACRONAL S 790, ACRONAL S 790 is possible to obtain highly filled systems (paints, plasters, putties, etc.) that do not lose their high consumer properties, while being cheaper in terms of the cost of ACRONAL S 790.
As a binder for nonwovens and textile coverings, ACRONAL S 790 is applied by impregnating, painting or spraying.

Use Areas of ACRONAL S 790:
Facade and interior paints
Texture coatings
Primers for mineral substrates
putty
Modifications of silicate paints
Means of concrete protection

Architectural coatings
Textured finishes
Interior paints
Exterior insulation and finishing systems (EIFS)
Grouts
Primers

Benefits of ACRONAL S 790:
APEO (Alkylphenol ethoxylate) free
High binding capacity
Good adhesion to various surfaces
Low water absorption
Wide range of applications

Advantages of ACRONAL S 790:
Broad formulation latitude
Exceptional cost-performance ratio
Outstanding saponification and alkaline resistance
Excellent water resistance
Superior dirt pick-up resistance

Processing of ACRONAL S 790:
Paints are produced in the usual way in high speed dissolvers.
Pigments and fillers are recommended to be first dispersed in the presence of wetting agents and dispersants (eg Pigment Dispersants N or A or water-soluble polyphosphates) before introducing the dispersion in an alkaline medium.
Only in the production of high viscosity, high solids products (eg texture coatings and fillers) which are produced in low speed mixers should ACRONAL S 790 be added along with the auxiliaries.

ACRONAL S 790 is characterized by high pigment absorption and excellent compatibility with fillers.
Exceptions are pigments that are difficult to crosslink, such as carbon black or calcium sulfate and zinc oxide, which can lead to high viscosity.

To control the viscosity and optimize the consumer properties of ACRONAL S 790, ACRONAL S 790 is usually necessary to add thickeners.
The most commonly used thickeners are cellulose ethers, polyacrylate or diurethane thickeners (eg Latecoll D or Collacral PU 75, PU 85, LR 8989, LR 8990) or bentonites and polysaccharides.
The choice of thickener depends on how the finished product should be (thixotropic or less viscous).

When pigments are used for coloring formulations, in particular in the form of pigment pastes (eg Luconyl brand), ACRONAL S 790 must be ensured that the thickener does not cause precipitation or flocculation of the pigments.
Therefore, ACRONAL S 790 is recommended to carry out compatibility tests (for storage) and, if necessary, the introduction of non-ionic surfactants (eg Lutensol AP 6 grades).

A small addition of LumitenNOC 30 improves compatibility with cement and lime, provides storage stability for highly pigmented interior paints in hard water applications, and facilitates cleaning of work tools.

For a successful film formation at temperatures below 20°C, the addition of coalescents such as white spirit, glycol ethers and Lusolvan FBH, SolvenonPP is recommended.
The recommended consumption is about 2% (based on the total volume).

To make the film particularly flexible, plasticizers can be added, e.g. Plastilit 3060 or chlorinated paraffin or phthalic acid ester.
ACRONAL S 790 is also possible to mix ACRONAL S 790 with soft dispersions (eg ACRONAL S 400) which promote the formation of a transparent film.

Mixing with dispersions based on pure acrylate or polyvinyl esters is also possible, but does not give a transparent film and does not offer any technical advantages.
The compatibility of ACRONAL S 790 with other dispersions is improved with the addition of CollacralVAL, a stabilizing protective colloid.

Like all fine dispersions, ACRONAL S 790 tends to foam.
Thus, ACRONAL S 790 is necessary to introduce antifoam agents in the amounts recommended by the manufacturers (approx. 0.3 - 1%).
The effectiveness of defoamers must be determined empirically.

Although ACRONAL S 790 is protected from attack by microorganisms, preservatives must be added to final products to ensure their stability during storage.
The compatibility and effectiveness of the preservative used should always be tested empirically.

Manufacturers should conduct their own rigorous product development trials using ACRONAL S 790 as our trials cannot cover the full range of factors that can influence product manufacturing and use (e.g. component compatibility, mixing process, adhesion to various substrates, and etc.)
Viscosity stability tests should also be carried out after storage at 50°C.

Storage of ACRONAL S 790:
ACRONAL S 790 during storage and processing should not come into contact with corrosive metals or their alloys without protective coatings.
Product containers must be tightly closed during storage and free air space above ACRONAL S 790 must be saturated with moisture.
ACRONAL S 790 must not be exposed to extreme heat or freezing.

To avoid problems with micro-organisms, the hygiene measures for product storage containers must be observed.

The shelf life of ACRONAL S 790 is 6 months when stored at 10 - 30 ºС

Safety of ACRONAL S 790:
The usual requirements for handling chemicals and local industrial hygiene regulations must be followed.
Efficient ventilation must be provided during processing, as well as personal protective equipment for the skin and goggles.

Properties of ACRONAL S 790:
Dispersion type: anionic
Solids content: ca. 50 %
pH value: ca. 7.5 – 9.0
Viscosity1: ca. 700–1.500 mPa·s
Average particle size: ca. 0.1 µm
MFFT: ca. 20 °C
Specific gravity (dispersion): ca. 1.04 g/cm³
Specific gravity (dry polymer): ca. 1.08 g/c

Product Cluster:
Dispersions

Product Group:
Styrene Acrylics

Industry:
Construction

Chemical type:
Styrene acrylics

Other ACRONAL Products:
ACRONAL TS 790
ACRONAL 290 D
ACRONAL T 290 D
ACRONAL S 562
ACRONAL S 562 T
ACRONAL ECO 6716
ACRONAL ECO 6716 T
ACRONAL PLUS 6727
ACRONAL S 813
ACRONAL ECO 6258
ACRONAL EDGE 6283
ACRONAL EDGE 6295
ACRONAL A 684
ACRONAL A 754
ACRONAL TA 754
ACRONAL PLUS 6257
ACRONAL DS
ACRONAL DS 6266
ACRONAL ECO 6270
ACRONAL LR 9014
ACRONAL TX 9014
ACRONAL TS 790
ACRONAL TS 790 is an aqueous styrene acrylic dispersion with medium viscosity and excellent pigment binding.

ACRONAL TS 790 is an anionic medium viscosity dispersion with a small particle size.
ACRONAL TS 790 has excellent compatibility with fillers and high pigment absorption.

Unpigmented ACRONAL TS 790 films do not exhibit surface tack at room temperature.
They are transparent, elastic, glossy, highly resistant to moisture and dirt.
ACRONAL TS 790 does not contain emulsifiers based on alkyl phenol ethoxylates.

ACRONAL TS 790 is a standard, universal binder for sealants and primers applications.
ACRONAL TS 790 shows a good filler compatibility and is compatible with many types of plasticizers.

ACRONAL TS 790 is an aqueous dispersion of a styrene acrylic copolymer with medium viscosity and excellent pigment binding power.

ACRONAL TS 790 is an APEO-free anionic styrene acrylic binder.
Has broad formulation latitude, medium viscosity and very good pigment binding capacity.

Offers exceptional cost performance and very good water resistance.
Exhibits outstanding saponification and alkaline resistance as well as superior dirt pick-up resistance.
ACRONAL TS 790 is used in architectural finishes, interior paints, textured finishes, primers, exterior insulation and finishing systems (EIFS) as well as grouts.

ACRONAL TS 790 acrylic dispersion is a styrene-acrylic dispersion (aqueous dispersion of an acrylic acid ester and styrene copolymer) for the manufacture of building paints (both exterior and interior), plasters and fillers, adhesives, used in the production of non-woven materials and textile coatings.

Application Area of ACRONAL TS 790:
A feature of ACRONAL TS 790 is its unique properties, thanks to which ACRONAL TS 790 is used for the manufacture of building paints from high gloss to matt, which can be applied to plaster, masonry, asbestos cement, concrete, wood and other substrates both inside and outside the building.
In addition, having an extremely high pigment capacity on ACRONAL TS 790, ACRONAL TS 790 is possible to obtain highly filled systems (paints, plasters, putties, etc.) that do not lose their high consumer properties, while being cheaper in terms of the cost of ACRONAL TS 790.
As a binder for nonwovens and textile coverings, ACRONAL TS 790 is applied by impregnating, painting or spraying.

Use Areas of ACRONAL TS 790:
Facade and interior paints
Texture coatings
Primers for mineral substrates
putty
Modifications of silicate paints
Means of concrete protection

Architectural coatings
Textured finishes
Interior paints
Exterior insulation and finishing systems (EIFS)
Grouts
Primers

Benefits of ACRONAL TS 790:
APEO (Alkylphenol ethoxylate) free
High binding capacity
Good adhesion to various surfaces
Low water absorption
Wide range of applications

Advantages of ACRONAL TS 790:
Broad formulation latitude
Exceptional cost-performance ratio
Outstanding saponification and alkaline resistance
Excellent water resistance
Superior dirt pick-up resistance

Processing of ACRONAL TS 790:
Paints are produced in the usual way in high speed dissolvers.
Pigments and fillers are recommended to be first dispersed in the presence of wetting agents and dispersants (eg Pigment Dispersants N or A or water-soluble polyphosphates) before introducing the dispersion in an alkaline medium.
Only in the production of high viscosity, high solids products (eg texture coatings and fillers) which are produced in low speed mixers should ACRONAL TS 790 be added along with the auxiliaries.

ACRONAL TS 790 is characterized by high pigment absorption and excellent compatibility with fillers.
Exceptions are pigments that are difficult to crosslink, such as carbon black or calcium sulfate and zinc oxide, which can lead to high viscosity.

To control the viscosity and optimize the consumer properties of ACRONAL TS 790, ACRONAL TS 790 is usually necessary to add thickeners.
The most commonly used thickeners are cellulose ethers, polyacrylate or diurethane thickeners (eg Latecoll D or Collacral PU 75, PU 85, LR 8989, LR 8990) or bentonites and polysaccharides.
The choice of thickener depends on how the finished product should be (thixotropic or less viscous).

When pigments are used for coloring formulations, in particular in the form of pigment pastes (eg Luconyl brand), ACRONAL TS 790 must be ensured that the thickener does not cause precipitation or flocculation of the pigments.
Therefore, ACRONAL TS 790 is recommended to carry out compatibility tests (for storage) and, if necessary, the introduction of non-ionic surfactants (eg Lutensol AP 6 grades).

A small addition of LumitenNOC 30 improves compatibility with cement and lime, provides storage stability for highly pigmented interior paints in hard water applications, and facilitates cleaning of work tools.

For a successful film formation at temperatures below 20°C, the addition of coalescents such as white spirit, glycol ethers and Lusolvan FBH, SolvenonPP is recommended.
The recommended consumption is about 2% (based on the total volume).

To make the film particularly flexible, plasticizers can be added, e.g. Plastilit 3060 or chlorinated paraffin or phthalic acid ester.
ACRONAL TS 790 is also possible to mix ACRONAL TS 790 with soft dispersions (eg ACRONAL S 400) which promote the formation of a transparent film.

Mixing with dispersions based on pure acrylate or polyvinyl esters is also possible, but does not give a transparent film and does not offer any technical advantages.
The compatibility of ACRONAL TS 790 with other dispersions is improved with the addition of CollacralVAL, a stabilizing protective colloid.

Like all fine dispersions, ACRONAL TS 790 tends to foam.
Thus, ACRONAL TS 790 is necessary to introduce antifoam agents in the amounts recommended by the manufacturers (approx. 0.3 - 1%).
The effectiveness of defoamers must be determined empirically.

Although ACRONAL TS 790 is protected from attack by microorganisms, preservatives must be added to final products to ensure their stability during storage.
The compatibility and effectiveness of the preservative used should always be tested empirically.

Manufacturers should conduct their own rigorous product development trials using ACRONAL TS 790 as our trials cannot cover the full range of factors that can influence product manufacturing and use (e.g. component compatibility, mixing process, adhesion to various substrates, and etc.)
Viscosity stability tests should also be carried out after storage at 50°C.

Storage of ACRONAL TS 790:
ACRONAL TS 790 during storage and processing should not come into contact with corrosive metals or their alloys without protective coatings.
Product containers must be tightly closed during storage and free air space above ACRONAL TS 790 must be saturated with moisture.
ACRONAL TS 790 must not be exposed to extreme heat or freezing.

To avoid problems with micro-organisms, the hygiene measures for product storage containers must be observed.

The shelf life of ACRONAL TS 790 is 6 months when stored at 10 - 30 ºС

Safety of ACRONAL TS 790:
The usual requirements for handling chemicals and local industrial hygiene regulations must be followed.
Efficient ventilation must be provided during processing, as well as personal protective equipment for the skin and goggles.

Properties of ACRONAL TS 790:
Dispersion type: anionic
Solids content: ca. 50 %
pH value: ca. 7.5 – 9.0
Viscosity1: ca. 700–1.500 mPa·s
Average particle size: ca. 0.1 µm
MFFT: ca. 20 °C
Specific gravity (dispersion): ca. 1.04 g/cm³
Specific gravity (dry polymer): ca. 1.08 g/c

Product Cluster:
Dispersions

Product Group:
Styrene Acrylics

Industry:
Construction

Chemical type:
Styrene acrylics

Other ACRONAL Products:
ACRONAL S 790
ACRONAL 290 D
ACRONAL T 290 D
ACRONAL S 562
ACRONAL S 562 T
ACRONAL ECO 6716
ACRONAL ECO 6716 T
ACRONAL PLUS 6727
ACRONAL S 813
ACRONAL ECO 6258
ACRONAL EDGE 6283
ACRONAL EDGE 6295
ACRONAL A 684
ACRONAL A 754
ACRONAL TA 754
ACRONAL PLUS 6257
ACRONAL DS
ACRONAL DS 6266
ACRONAL ECO 6270
ACRONAL LR 9014
ACRONAL TX 9014
ACRONAL TS 790
ACRONAL TS 790 is a chemical compound that belongs to the isothiazolinone family.
ACRONAL TS 790 metalwork fluid is a mixture of the two isothiazoliones contained in Kathon CG, at a 13.9% concentration.
ACRONAL TS 790 helps to inhibit the growth of harmful microorganisms.

CAS Number: 55965-84-9
Molecular Formula: C4H5NOS.C4H4ClNOS
Molecular Weight: 264.756
EINECS Number: 911-418-6

ACRONAL TS 790 is mainly contained in metalwork fluids.
As an active component of Aigezid Ⅱ and ACRONAL TS 790 contained in a water bath used for phtotographic development, it caused contact dermatitis in a photograph developer.

ACRONAL TS 790 is a mixture of isothiazolinone-derived biocides.
ACRONAL TS 790 is effective against Gram-positive and Gram-negative bacteria values of 0.0002, 0.0002, 0.00005, and 0.00005% (w/w).
ACRONAL TS 790 can elicit contact sensitization.

Formulations containing ACRONAL TS 790 have been used for controlling microbial growth in industrial and household products.
ACRONAL TS 790, is a combination of two synthetic preservatives used in various personal care, household, and industrial products.
These preservatives are antimicrobial agents that help prevent the growth of bacteria, fungi, and other microorganisms in products, thereby extending their shelf life and maintaining their quality.

The combination of ACRONAL TS 790T creates a synergistic effect, enhancing the overall antimicrobial activity of the mixture.
By combining two different antimicrobial agents, the preservative can target a broader range of microorganisms, providing more comprehensive protection.
ACRONAL TS 790 use Levels and Concentrations; the concentrations of ACRONAL TS 790 in products can vary based on the intended use, the type of product, and regulatory guidelines.

ACRONAL TS 790 manufacturers follow recommended use levels to ensure effective preservation while minimizing the potential for adverse reactions.
ACRONAL TS 790 helps maintain the stability and quality of products by preventing the growth of microorganisms that could degrade the product's components.
There have been reports of allergic contact dermatitis associated with ACRONAL TS 790-containing products.

This has led to regulatory actions and increased scrutiny of their use.
In response to concerns, some manufacturers have reformulated their products to reduce or eliminate the use of ACRONAL TS 790.
In regions where ACRONAL TS 790 is perACRONAL TS 790ted, regulations often require that products containing these preservatives be properly labeled to inform consumers and allow those with sensitivities to make informed choices.

Manufacturers conduct preservative efficacy testing to ensure that the chosen concentration of ACRONAL TS 790 effectively prevents microbial growth over the shelf life of the product.
The debate about the safety and sensitization potential of ACRONAL TS 790 has prompted the cosmetic and personal care industry to explore alternative preservatives that have lower risks of allergic reactions.
Natural preservatives, antioxidants, and other synthetic alternatives are being investigated as potential replacements.

ACRONAL TS 790 and MI are chemical compounds commonly used as preservatives in various personal care and household products.
They are part of a group of chemicals known as isothiazolinones, which are used to extend the shelf life of products by preventing the growth of bacteria, yeasts, and molds.

ACRONAL TS 790 has antimicrobial properties and is often used as a preservative in products like shampoos, conditioners, liquid soaps, and other water-based cosmetic and personal care items.
ACRONAL TS 790 helps to prevent the growth of microorganisms that can lead to product spoilage or contamination.

ACRONAL TS 790 is another isothiazolinone compound commonly used as a preservative.
ACRONAL TS 790 is closely related to MI and has similar antimicrobial properties.
ACRONAL TS 790 is used in a wide range of products, including cosmetics, skincare products, detergents, paints, and industrial products.

Both ACRONAL TS 790 and MI have been associated with potential health concerns, particularly in terms of skin sensitization and allergic reactions.
Some individuals may develop allergic contact dermatitis upon exposure to products containing these compounds.

Due to the observed health concerns, regulatory agencies in various countries have taken actions to regulate the use of ACRONAL TS 790 and MI in consumer products.
In the European Union, for example, certain concentrations of ACRONAL TS 790 and MI are restricted in leave-on cosmetic products, which are products meant to remain on the skin after application, such as lotions and creams.
This regulation is in response to the reported cases of skin sensitization.

In many countries, products that contain ACRONAL TS 790 or MI must be labeled appropriately to inform consumers about their presence.
This allows individuals with known sensitivities or allergies to avoid products containing these compounds.
Given the potential skin sensitization risks associated with ACRONAL TS 790 and MI, many manufacturers have started to reformulate their products to use alternative preservatives.

Form: liquid, dispersion
Colour: white
Odour: almost odourless
pH value: 7,5 - 9,0 (23 °C)
Information on: Water
Melting point: 0 °C
Information on: Water
Boiling point: 100 °C
Flash point: not applicable
Flammability: not flammable
Lower explosion liACRONAL TS 790: For liquids not relevant for classification and labelling.
Information on: Water
Vapour pressure: 23,4 hPa (20 °C)
Density: approx. 1,0 g/cm3 (20 °C)
Solubility in water: partly soluble (15 °C)
Specific gravity (dispersion): ca. 1.04 g/cm³
Specific gravity (dry polymer): ca. 1.08 g/cm³

ACRONAL TS 790 works by disrupting the cell membranes of microorganisms, which leads to cell leakage and death.
This mode of action inhibits the growth and reproduction of bacteria and fungi.
ACRONAL TS 790 is a widely used antimicrobial preservative combination found in personal care, household, and industrial products.

ACRONAL TS 790 helps prevent microbial contamination, prolonging the shelf life and maintaining the quality of various formulations.
ACRONAL TS 790 acts both as a microbiostatic agent (inhibiting microbial growth) and a microbicidal agent (killing existing microorganisms).
This dual action helps maintain the integrity of products.

While ACRONAL TS 790 effectively prevents microbial growth, its use can be challenging due to the potential for allergic reactions in some individuals.
The industry has faced pressure to find alternatives that maintain the benefits of microbial protection without causing sensitization issues.
Manufacturers sometimes use ACRONAL TS 790 in combination with other preservatives to achieve a broader spectrum of antimicrobial activity and reduce the concentration of each individual preservative.

ACRONAL TS 790's compatibility with other ingredients in product formulations is important to maintain the overall stability and efficacy of the final product.
Regulatory authorities have introduced restrictions and guidelines for the use of ACRONAL TS 790 due to the reported cases of allergic contact dermatitis.
In some cases, certain product categories or concentrations of ACRONAL TS 790 have been prohibited or liACRONAL TS 790ed.

Patch testing is used to determine an individual's sensitivity or allergy to ACRONAL TS 790, helping to identify potential risks of adverse reactions.
Raising consumer awareness about the presence of ACRONAL TS 790 in products and the importance of patch testing can empower individuals to make informed choices.
Certain populations, such as infants, children, and individuals with sensitive or compromised skin, may be more susceptible to reactions from ACRONAL TS 790-containing products.

The potential for sensitization to ACRONAL TS 790 can be influenced by factors such as concentration in the product, frequency of exposure, individual skin sensitivity, and the presence of other allergens.
Dermatologists and allergists use patch testing to identify sensitization to specific allergens, including ACRONAL TS 790.
This helps individuals make informed choices about product usage.

Some individuals prone to sensitization may follow a preservative rotation strategy, using products with different preservatives to minimize the risk of developing allergies.
The use of ACRONAL TS 790 in products intended for children has raised concerns due to the potential for sensitization in young and sensitive skin.
Regulations and guidelines may vary for these products.

Uses
ACRONAL TS 790 used in antimicrobial preservative in cosmetics, hygeine products, paints, emulsions, cutting oils, paper coatings, and water storage and cooling units.
ACRONAL TS 790 is a chemical compound used as a preservative in various products.
ACRONAL TS 790 has broad-spectrum antimicrobial activity against bacteria and fungi.

ACRONAL TS 790s are particularly effective in water-based products, where the presence of water can create an environment conducive to microbial growth.
ACRONAL TS 790 and MI can be used in water treatment to inhibit the growth of microorganisms in water systems, such as cooling towers and industrial water supplies.
ACRONAL TS 790 is used in some textile and fabric treatments to prevent the growth of microorganisms that can cause odors or degradation.

ACRONAL TS 790 is commonly found in personal care products such as shampoos, conditioners, body washes, lotions, creams, and cosmetics.
It prevents the growth of bacteria, yeast, and fungi, helping maintain product hygiene and quality.
ACRONAL TS 790 is used in household cleaning products like detergents, fabric softeners, disinfectants, and surface cleaners to inhibit microbial growth and maintain product effectiveness.

ACRONAL TS 790 is used in industrial formulations, including paints, adhesives, and coatings, to prevent the degradation caused by microorganisms.
ACRONAL TS 790's used in water-based products where microbial contamination is a concern, such as liquid soaps, body washes, and shampoos.
ACRONAL TS 790 is included in wet wipes to ensure their freshness and microbial safety.

ACRONAL TS 790 and MI can be found in some pet care products, such as shampoos and grooming supplies, to preserve their quality and safety.
Some automotive products, including car wash solutions and interior cleaners, may contain ACRONAL TS 790 and MI to prevent microbial growth and maintain product efficacy.
In some cases, ACRONAL TS 790 and MI are used in medical and healthcare settings where microbial control is essential.

They can be present in certain types of disinfectants, medical device cleaners, and hand sanitizers.
ACRONAL TS 790 and MI are sometimes used in photographic chemicals to prevent microbial contamination and maintain the stability of these products.
In industrial processes such as metalworking, ACRONAL TS 790 and MI can be added to cutting fluids and coolants to inhibit the growth of microorganisms that could affect machining operations.

ACRONAL TS 790 and MI can be found in cleaning wipes and towelettes that are intended to disinfect and sanitize surfaces.
Wet wipes in various applications, including personal care and cleaning, might contain ACRONAL TS 790 and MI to prevent bacterial and fungal growth in the moist environment.
ACRONAL TS 790 and MI are used in some water-based paints and coatings to prevent spoilage and maintain product quality.

ACRONAL TS 790's used in cosmetics such as makeup removers, facial cleansers, and moisturizers to maintain product stability and quality.
ACRONAL TS 790 helps prevent the growth of microorganisms in hair care products like conditioners and hair styling products.
In various industrial products, such as cutting fluids and metalworking fluids, ACRONAL TS 790 inhibits microbial growth, contributing to the maintenance of product performance.

ACRONAL TS 790 can be found in laundry detergents to prevent the growth of odor-causing bacteria and fungi in fabrics.
ACRONAL TS 790's used in automotive and industrial cleaning products to ensure that they remain free from microbial contamination.
ACRONAL TS 790 is utilized in adhesives and sealants to prevent microbial growth that could compromise the integrity of the products.

ACRONAL TS 790's used in some paper products to prevent the growth of mold and other microorganisms.
ACRONAL TS 790 is another antimicrobial compound that is often used in combination with ACRONAL TS 790T.
It provides additional antimicrobial protection against a wide range of microorganisms.

ACRONAL TS 790 is commonly found in a variety of personal care products, including shampoos, conditioners, body washes, lotions, creams, and cosmetics.
Its presence helps prevent the growth of microorganisms in these products, reducing the risk of contamination.

ACRONAL TS 790 is used in household products such as detergents, fabric softeners, and cleaning solutions to maintain product quality and safety by inhibiting microbial growth.
ACRONAL TS 790 is also used in industrial settings, where it prevents the proliferation of microorganisms in various formulations, including paints, adhesives, and industrial cleaners.

Environmental Considerations
Like other synthetic chemicals, ACRONAL TS 790 has raised concerns about its environmental impact when released into the environment, such as through wastewater.
Industry efforts are being directed toward developing more environmentally friendly preservatives and sustainable practices.

Safety
One of the most significant hazards of ACRONAL TS 790 and MI is their potential to cause skin sensitization.
Skin sensitization is an allergic reaction that occurs when the immune system becomes sensitized to a specific substance, resulting in the development of an allergic response upon subsequent exposure.
People who become sensitized to ACRONAL TS 790 and MI can develop contact dermatitis, which manifests as redness, itching, rash, and other skin irritations.

Allergic Reactions
Individuals who are sensitized to ACRONAL TS 790 and MI may experience allergic reactions upon exposure, even at low concentrations.
Allergic reactions can vary in severity and may lead to discomfort, pain, and a decreased quality of life for affected individuals.

Synonyms
55965-84-9
ACRONAL TS 790
Kathon biocide
Kathon CG
Bio-Perge
Kathon LX
Kathon WT
Zonen F
ProClin 300
Microcide III
Somacide RS
Legend MK
ACRONAL TS 790MW
Kathon CG/ICP II
Slaoff 360
ACRONAL TS 790 W
Kathon RH 886
MBC 215
Tret-O-Lite XC 215
2-Methylisothiazol-3(2H)-one compound with 5-chloro-2-methylisothiazol-3(2H)-one(14%in H2O)
CCRIS 4652
KKM 43
Isothiazolinone chloride
EPA Pesticide Chemical Code 107103
5-chloro-2-methyl-1,2-thiazol-3-one;2-methyl-1,2-thiazol-3-one
5-Chloro-2-methyl-3(2H)-isothiazolone mixt. with 2-methyl-3(2H)-isothiazolone
2-Methylisothiazol-3(2H)-one compound with 5-chloro-2-methylisothiazol-3(2H)-one (1:1)
3(2H)-Isothiazolone, 5-chloro-2-methyl-, mixt. with 2-methyl-3(2H)-isothiazolone
3(2H)-Isothiazolone, 5-chloro-2-methyl-, mixt. with2-methyl-3(2H)-isothiazoloneOTHER CA INDEX NAMES:3(2H)-Isothiazolone, 2-methyl-, mixt. contg.
C8H9ClN2O2S2
2-Methylisothiazol-3(2H)-one 5-chloro-2-methylisothiazol-3(2H)-one (1:1)
C4H5NOS.C4H4ClNOS
SCHEMBL348332
UNII-15O9QS218W
CHEMBL108095
ACRONAL TS 790 (Kathon Biocide)
C(M)IT/ACRONAL TS 790 (3:1)
QYYMDNHUJFIDDQ-UHFFFAOYSA-N
15O9QS218W
AKOS016842708
CS-W018768
70294-89-2
CS-17384
LS-86321
PD151064
C4-H5-N-O-S.C4-H4-Cl-N-O-S
Q26841195
2-Methylisothiazol-3(2H)-one 5-chloro-2-Methylisothiazol-3(2H)-one
2-Methylisothiazol-3(2H)-one 5-chloro-2-methylisothiazol-3(2H)-one (1:1) 14% in water
2-Methylisothiazol-3(2H)-one compound with 5-chloro-2-methylisothiazol-3(2H)-one
2-Methylisothiazol-3(2H)-onecompoundwith5-chloro-2-methylisothiazol-3(2H)-one(14%inH2O)
2-METHYLISOTHIAZOL-3(2H)-ONE COMPOUND WITH 5-CHLORO-2-METHYLISOTHIAZOL-3(2H)-ONE(14% IN H2O)
ACRONAL V 275
ACRONAL V 275 ACRONAL V 275 ACRONAL V 275 is a high solids acrylic binder used in flooring adhesives and specialty sealants. ACRONAL V 275 is ammonia-free and offers high cohesive strength, good plasticizer resistance, and filler acceptance. Acronal V 275 Technical Datasheet Acronal V 275 is an acrylic/vinyl acetate copolymer emulsion. Used in adhesives for laying PVC floor coverings & carpets with many different backings and specialty sealants. Acronal V 275 na offers high tack, good quick grab, heat stability, good plasticizer migration resistance and good filler acceptance. Product Type Acrylics & Acrylic Copolymers Physical Form Emulsion Product Status COMMERCIAL Acronal V 275 na is a high solids acrylic used in flooring adhesives and specialty sealants. It offers high cohesive strength, good plasticizer resistance, and filler acceptance. This product is ammonia free. Technical Information Construction Chemicals Acronal V 275 Aqueous polymer dispersion for the manufacture of adhesives & sealants for theConstruction industry. Acronal 81 D is an acrylic dispersion. Used in elastic sealants as gap fillers. Acronal® 81 D improves the coherence of expandable foams.
ACRYLAMIDE
SYNONYMS 2-Propenamide, polymer with N,N,N-trimethyl-3-(2-propenamido)propanaminium chloride;1-Propanaminium, N,N,N-trimethyl-3-((1-oxo-2-propen-1-yl)amino)-, chloride (1:1), polymer with 2-propenamide;1-Propanaminium, N,N,N-trimethyl-3-((1-oxo-2-propenyl)amino)-, chloride, polymer with 2-propenamide CAS NO:75150-29-7
ACRYLAMIDE (2-PROPENAMIDE)
Acrylamide (2-Propenamide), in monomeric form, is an odorless, flake-like crystals which sublime slow at room temperature.
Acrylamide (2-Propenamide) may be dissolved in a flammable liquid.
Acrylamide, also known as 2-Propenamide, is an industrial chemical and can also form from naturally-occurring components of certain foods when cooked at high temperatures.

CAS Number: 79-06-1
Molecular Formula: C3H5NO
Molecular Weight: 71.08
EINECS Number: 201-173-7

Acrylamide (2-Propenamide) is an organic compound with the chemical formula CH2=CHC(O)NH2.
Acrylamide (2-Propenamide) is a white odorless solid, soluble in water and several organic solvents.
From the chemistry perspective, Acrylamide (2-Propenamide) is a vinyl-substituted primary amide (CONH2).

Acrylamide (2-Propenamide) is produced industrially mainly as a precursor to polyacrylamides, which find many uses as water-soluble thickeners and flocculation agents.
Acrylamide (2-Propenamide) forms in burnt areas of food, particularly starchy foods like potatoes, when cooked with high heat, above 120 °C (248 °F).
Despite health scares following its discovery in 2002, dietary acrylamide is thought unlikely to be carcinogenic for humans; Cancer Research UK categorized the idea that burnt food causes cancer as a "myth".

Acrylamide, also known as 2-propenamide or acrylic amide, is a chemical substance has a role in making polyacrylamide, which in turn is used in inks, in flocculants for water treatment, in cement production and the production of plastics.
Acrylamide (2-Propenamide), is a chemical compound with the molecular formula C3H5NO.
It is a colorless, odorless, crystalline solid that is highly soluble in water.

Acrylamide (2-Propenamide) is an organic compound that contains a vinyl group (CH2=CH-) and an amide group (CONH2) in its chemical structure.
Acrylamide (2-Propenamide) is a white crystalline chemical substance and is a raw material for production of polyacrylamide.
Solid Acrylamide (2-Propenamide) is usually colorless and transparent flaky crystals with pure product being white crystalline solid which is soluble in water, methanol, ethanol, propanol, and slightly soluble in ethyl acetate, chloroform, and benzene.

Acrylamide (2-Propenamide) can be hydrolyzed to acrylic acid in acidic or alkaline environment.
Acrylamide (2-Propenamide) is a large class of the parent compound of monomers including methacrylamide, the AMPS (anionic monomer, 2-Acraylamide-2-Methyl Propane Sulfonic Acid), the DMC (cationic monomer, methyl-acryloyloxyethyl trimethyl ammonium chloride) and N-substituted acrylamide compound.

Occupational exposure is mainly seen in acrylamide production and the synthesis of resins, adhesives, etc.
Acrylamide (2-Propenamide) is also possible for contract in underground construction, upon soil improvement, painting, paper industry and garment processing.
At daily life, people can touch Acrylamide (2-Propenamide) in smoking, drinking and eating the starchy foods processed at high temperature.

Acrylamide (2-Propenamide) is an odorless, white crystalline solid that initially was produced for commercial purposes by reaction of acrylonitrile with hydrated sulfuric acid.
Acrylamide (2-Propenamide) exists in two forms: a monomer and a polymer.
Monomer Acrylamide (2-Propenamide) readily participates in radicalinitiated polymerization reactions, whose products form the basis of most of its industrial applications.

The single unit form of Acrylamide (2-Propenamide) is toxic to the nervous system, a carcinogen in laboratory animals and a suspected carcinogen in humans.
The multiple unit or polymeric form is not known to be toxic.
Acrylamide (2-Propenamide) is formed as a by-product of the Maillard reaction.

The Maillard reaction is best known as a reaction that produces pleasant flavor, taste, and golden color in fried and baked foods; the reaction occurs between amines and carbonyl compounds, particularly reducing sugars and the amino acid asparagine.
In the first step of the reaction, asparagine reacts with a reducing sugar, forming a Schiff’s base.
Acrylamide (2-Propenamide) is formed following a complex reaction pathway that includes decarboxylation and a multistage elimination reaction.

Acrylamide (2-Propenamide) formation in bakery products, investigated in a model system, showed that free asparagine was a limiting factor.
Treatment of flours with asparaginase practically prevented acrylamide formation.
Coffee drinking and smoking are other major sources apart from the human diet.

Acrylamide (2-Propenamide) is odorless and colorless crystal.
Acrylamide (2-Propenamide) is soluble in water, ethanol, acetone, ether, and methyl chloroform, and slightly soluble in toluene but insoluble in benzene.
Acrylamide (2-Propenamide) is a water-soluble monomer with two reactive centers (a vinyl group - with its reactive double bond, and an amide group).

Because of its high reactivity, aqueous Acrylamide (2-Propenamide) is stabilized with dissolved cupric salts and oxygen to prevent polymerization during shipping and storage.
Acrylamide (2-Propenamide) can form in certain foods during cooking processes that involve high temperatures, particularly when the Maillard reaction occurs.
The Maillard reaction is a complex chemical reaction between amino acids and reducing sugars, and it's responsible for the browning and development of flavors in various cooked foods.

Acrylamide (2-Propenamide) is one of the byproducts of this reaction.
French fries, potato chips, and roasted potatoes are known to contain relatively high levels of Acrylamide (2-Propenamide), especially if they are cooked to a dark brown or crispy texture.
Foods made from grains, such as breakfast cereals, bread, and cookies, may also contain Acrylamide (2-Propenamide) when they are baked or toasted.

Roasted coffee beans can contain Acrylamide (2-Propenamide), although the levels are typically lower than in some other foods.
Various types of snack foods, including crackers and pretzels, can contain Acrylamide (2-Propenamide).
Food producers and processors have implemented various strategies to reduce Acrylamide (2-Propenamide) levels in their products.

Modifying the type of ingredients used in food formulations, such as using low-sugar varieties or blanched potatoes, can help reduce Acrylamide (2-Propenamide) formation during cooking.
Adjusting cooking parameters like temperature, time, and cooking methods can minimize Acrylamide (2-Propenamide) formation.
For example, using lower frying temperatures or shorter cooking times can help reduce Acrylamide (2-Propenamide) levels.

Some foods undergo preprocessing steps like soaking, blanching, or parboiling before the final cooking stage to reduce Acrylamide (2-Propenamide) formation.
Certain enzymes can be added to food products to break down precursors of Acrylamide (2-Propenamide), reducing its formation during cooking.
Proper packaging and storage of foods can also play a role in Acrylamide (2-Propenamide) reduction.

For example, storing potatoes in a cool, dark place can help prevent the formation of sprouts, which contain higher levels of acrylamide precursors.
Different countries and regions have established regulatory standards and guidelines related to Acrylamide (2-Propenamide) in food.
These standards often include maximum allowable levels of Acrylamide (2-Propenamide) in specific food products.

Acrylamide (2-Propenamide) and its potential health implications has increased over the years.
Public health agencies and organizations often provide information to consumers on how to make informed choices about their diets.
This includes understanding which foods are more likely to contain Acrylamide (2-Propenamide) and how to minimize exposure through cooking and food choices.

Research on Acrylamide (2-Propenamide) continues to evolve, with ongoing studies aimed at better understanding its health effects and how to reduce its presence in food.
Scientists are investigating the potential health risks associated with long-term, low-level dietary exposure to Acrylamide (2-Propenamide), and research findings may lead to adjustments in regulatory standards and dietary recommendations.

Melting point: 82-86 °C(lit.)
Boiling point: 125 °C25 mm Hg(lit.)
Density: 1,322 g/cm3
vapor density: 2.45 (vs air)
vapor pressure: 0.03 mm Hg ( 40 °C)
refractive index: 1.460
Flash point: 138 °C
storage temp.: 2-8°C
solubility: 2040 g/L (25°C)
form: powder
pka: 15.35±0.50(Predicted)
color: White
Odor: Odorless solid
PH: 5.0-7.0 (50g/l, H2O, 20℃)
Water Solubility: Acrylamide is routinely tested at 250 mg/mL in water, giving a clear colorless solution, It is soluble at least to 40% (w/v) in water, and reportedly up to 215 g/100 mL in water at 30°C.
Sensitive: Light Sensitive
Merck: 14,129
BRN: 605349
Stability: Unstable. Do not heat above 50C, Explosive, Incompatible with acids, bases, oxidizing agents, reducing agents, iron and iron salts, copper, aluminium, brass, free radical initiators, Air sensitive, Hygroscopic.
InChIKey: HRPVXLWXLXDGHG-UHFFFAOYSA-N
EPA Primary Drinking Water Standard MCL:TT4,MCLG:zero
LogP: -0.9 at 20℃ and pH7

Acrylamide (2-Propenamide) was discovered in foods, mainly in starchy foods, such as potato chips (UK: potato crisps), French fries (UK: chips), and bread that had been heated higher than 120 °C (248 °F).
Production of Acrylamide (2-Propenamide) in the heating process was shown to be temperature-dependent.
Acrylamide (2-Propenamide) was not found in food that had been boiled, or in foods that were not heated.

Acrylamide (2-Propenamide) has been found in roasted barley tea, called mugicha in Japanese.
The barley is roasted so it is dark brown prior to being steeped in hot water.
The roasting process produced 200–600 micrograms/kg of acrylamide in mugicha.

This is less than the >1000 micrograms/kg found in potato crisps and other fried whole potato snack foods cited in the same study and it is unclear how much of this is ingested after the drink is prepared.
Rice cracker and sweet potato levels were lower than in potatoes.
Potatoes cooked whole were found to have significantly lower Acrylamide (2-Propenamide) levels than the others, suggesting a link between food preparation method and acrylamide levels.

Acrylamide (2-Propenamide) levels appear to rise as food is heated for longer periods of time.
Although researchers are still unsure of the precise mechanisms by which Acrylamide (2-Propenamide) forms in foods, many believe it is a byproduct of the Maillard reaction.
In fried or baked goods, acrylamide may be produced by the reaction between asparagine and reducing sugars (fructose, glucose, etc.) or reactive carbonyls at temperatures above 120 °C (248 °F).

Acrylamide (2-Propenamide) may decompose with heat and polymerize at temperatures above 84 C, or exposure to light, releasing ammonia gas.
Reacts violently with strong oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions.
Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

Synthesis
At the end of 19th century, people had first made Acrylamide (2-Propenamide) using propylene chloride and ammonia.
In 1954, American Cyanamid Company uses sulfuric acid hydrolysis of acrylonitrile for industrial production.
In 1972, Mitsui Toatsu Chemicals, Inc. had first established the skeleton copper (see the metal catalyst) catalyzed Acrylamide (2-Propenamide) synthesis via acrylonitrile hydration.

Then other countries have developed different types of catalyst and applied this technology for industrial production.
In 1980s, Japanese Nitto Chemical Industry Company has achieved that using biological catalyst for industrial production of Acrylamide (2-Propenamide) from acrylonitrile.

Acrylonitrile and water is hydrolyzed into Acrylamide (2-Propenamide) sulfate in the presence of sulfuric acid and then treated neutralized liquid ammonia to give ammonium sulfate and acrylamide:
CH2 = CHCN + H2O + H2SO4 → CH2 = CHCONH2 • H2SO4 CH2 = CHCONH2 • H2SO4 + 2NH3→ CH2 = CHCONH2 + (NH4) 2SO4
The disadvantage of this method is by-producing a large number of low-value, low fertilizing efficacy-ammonium sulfate and causing serious sulfuric acid corrosion and pollution.

Acrylonitrile is reacted with water by the copper-based catalyst to have liquid phase hydration reaction at 70~120 °C at 0.4MPa pressure.
CH2 = CH-CN + H2O → CH2 = CHCONH2; Filter the catalyst after reaction catalyst; recycle the unreacted acrylonitrile; Acrylamide (2-Propenamide) solution was concentrated and cooled to give crystals.
This is a simple method with the yield up to 98%.

Production methods
Acrylonitrile sulfate hydration; Acrylonitrile and water is hydrolyzed into acrylamide sulfate in the presence of sulfuric acid and then treated neutralized liquid ammonia to give ammonium sulfate and Acrylamide (2-Propenamide): The reaction products further undergoes filtering and separation.
Crystallize the filtrate, dry to obtain the final product.

The disadvantage of this method is by-producing a large number of low-value, low fertilizing efficacy-ammonium sulfate and causing serious sulfuric acid corrosion and pollution.
This method can produce by-products of 2280 kg ammonium sulfate in per tons of acrylonitrile.
Material consumption amount: Acrylonitrile (100%) 980kg/t, sulfuric acid (100%) 200kg/t, ammonia (100%) 700kg/t.

Direct hydration of acrylonitrile: acrylonitrile is directly hydrated by water with copper being the catalyst at 85-125 °C and 0.3-0.4MPa pressure.
The yielding aqueous solution of Acrylamide (2-Propenamide) (containing only small amounts of by-products) can be directly sold as a finished product.
This method avoids Acrylamide (2-Propenamide) dust pollution and is advantageous for labor protection for using aqueous solution.

Reference Product Specifications: appearance: white flakes or powder.
With first-grade product containing content ≥95%; Secondary-grade content ≥90%; grade III content ≥85%.
Enzyme catalysis; at room temperature transfer the acrylonitrile solution into the fixed-bed reactor containing bacteria catalyst; after the reaction, 100% of acrylonitrile is converted into Acrylamide (2-Propenamide).

After isolation and even without the necessity of refining and concentration.
Concentrated sulfuric acid hydration method: mixture containing sulfate, phenothiazine (polymerization inhibitor), and water is added to the reactor; stir slowly with dropping acrylonitrile After the addition is completed, raise the temperature to 95~100 °C, keep the temperature for 50 min.
Cool to 20~25 °C, dilute with an appropriate amount of water, neutralize with sodium carbonate, filtrate to obtain aqueous acrylic acid solution.

Further cool and crystallize, separate, dry to obtain the completed products.
Catalytic hydration method; acrylonitrile and water undergoes liquid phase hydration in the presence of copper-based catalyst; It is generally used for continuous production with the reaction temperature being 85~120 °C, reaction pressure being 0.29~0.39 MPa, feed concentration of 6.5%, airspeed being 5 L/ h, the conversion rate being 85%, and selectivity being about 95% and the concentration of acrylamide in the reaction being 7% to 8%.

Aqueous solution obtained by this method may be directly used as the product for sale.
Acrylamide (2-Propenamide) can be prepared by the hydration of acrylonitrile, which is catalyzed enzymatically:
CH2=CHCN + H2O → CH2=CHC(O)NH2

This reaction also is catalyzed by sulfuric acid as well as various metal salts.
Treatment of acrylonitrile with sulfuric acid gives acrylamide sulfate, CH=CHC(O)NH2·H2SO4.
This salt can be converted to acrylamide]with base or to methyl acrylate with methanol.

Uses
Acrylamide (2-Propenamide) can be used as a monomer of polyacrylamide.
Its polymer or copolymer is used as chemical grouting materials, soil conditioners, flocculants, adhesives and coatings.
Polyacrylamide, when used as a kind of additive, can improve the oil recycling efficiency.

When used as flocculants, Acrylamide (2-Propenamide) can be used for sewage treatment.
Acrylamide (2-Propenamide) can also be used as a paper strength agent.
Acrylamide (2-Propenamide) is the most important products in acrylamide and methacrylamide-based products.

Since its application in industry in 1954, the demand gradually increase.
Acrylamide (2-Propenamide) is mainly used for the preparation of water soluble polymers which can be used as additives to improve oil recovery; as a flocculant, thickening agents, and paper additives.
A small amount of Acrylamide (2-Propenamide) is introduce the hydrophilic center into the lipophilic polymer to improve the viscosity, increase the softening point and improve anti-solvents ability of resin, and can aso introduce a center for the coloring property of dye.

Acrylamide (2-Propenamide) is also often used as a component of the photopolymer.
For the vinyl polymer, its crosslinking reaction can take advantage of this kind of reactive amide groups.
Acrylamide (2-Propenamide) can co-polymerizze with certain monomers such as vinyl acetate, styrene, vinyl chloride, vinylidene chloride, and acrylonitrile to obtain a polymer with a variety of applications.

The main application areas: used for the oilfield; the materials can be used in oilfield injection of wells for adjustment of the injection profile.
Mix this product with initiator, and deaerator and inject into the high permeability layer part of water wells.
This will lead the formation of high-viscosity polymer unearth of the stratum.

This can plug the large pore, increase the swept volume of oil, and enhance the oil recovery.
In addition, the product polymer or copolymer can be used for tertiary oil recovery, fracturing, water shutoff, drilling mixing process and chemical grouting.
Acrylamide (2-Propenamide) can be used as flocculants.

Acrylamide (2-Propenamide) partially hydrolyzed product and its graft copolymer of methyl cellulose can be used in wastewater treatment and sewage treatment.
Soil conditioner; using the hydrolyzed product as soil amendments can aggregate soil and can improve air circulation, water permeability and water retention.
Modification of fiber and resin processing; using acrylamide for carbamylation or graft polymerization can improve the resin arrangement of a variety of fiber containing synthetic fiber, as well as for warp and printing paste in order to improve the basic physical properties of fabrics as well as preventing wrinkle, shrink and keeping a good hand feeling.

Acrylamide (2-Propenamide) can be used as paper enhancer; copolymer of acrylamide and acrylic acid or partial hydrolysis products of polyacrylamide can be used as paper strength reinforcing agent for either replacing or combining with starch, and water-soluble amino resin.
Acrylamide (2-Propenamide) can be used as an adhesive agent including glass fiber adhesive agent with the combination of phenolic resin and polyacrylamide solution, as well as pressure sensitive adhesive combined with synthetic rubber.

Acrylamide (2-Propenamide) is the raw material for producing polyacrylamide and related products.
Acrylamide (2-Propenamide) can be used as the monomer of polyacrylamide.
Acrylamide (2-Propenamide)s polymer or copolymer can be used as chemical grouting materials, soil conditioners, flocculants, adhesives and coatings.

Polyacrylamide, as an additive, can improve oil recovery. As a kind of flocculants, it can be used for waste water treatment as well as paper strength enhancer can.
Acrylamide (2-Propenamide) is the raw material for producing polyacrylamide and related products.
Acrylamide (2-Propenamide) can also used for determining the relative molecular weight of acid.

The majority of Acrylamide (2-Propenamide) is used in the manufacture of various polymers, which in turn are used as binding, thickening, or flocculating agents in grout, cement, sewage/waste water treatment, pesticide formulations, cosmetics, sugar manufacturing and soil erosion prevention, ore processing, food packaging, plastic products and in molecular biology laboratory applications.
In Canada, polyacrylamide is used as a coagulant and flocculant for the clarification of drinking water; Acrylamide (2-Propenamide) is also used in potting soils and as a non-medicinal ingredient in natural health products and pharmaceuticals.

Over 90% of Acrylamide (2-Propenamide) is used to make polyacrylamides (PAMs), and the remaining 10% is used to make N-methylolacrylamide (NMA) and other monomers.
Water treatment PAMs consumed 60% of the Acrylamide (2-Propenamide); PAMs for pulp and paper production consume 20% of the acrylamide; and PAMs for mineral processing consume 10% of the acrylamide.
In liquid-solid separation where Acrylamide (2-Propenamide) polymers act as flocculants and aids in mineral processing, waste treatment and water treatment.

They also help reduce sludge volumes in these applications.
As additives in the manufacture of paper and paper board products, leather and paint industries.
In the paper industry Acrylamide (2-Propenamide)s act as retention aids during wet end processing and in wet strength additives.

In the manufacture of synthetic resins for pigment binders for textile/leather industries, and In enhanced oil recovery.
Acrylamide (2-Propenamide) is used in protein electrophoresis (PAGE), synthesis of dyes and copolymers for contact lenses.
Acrylamide (2-Propenamide) is reasonably anticipated to be a hum an carcinogen.

The majority of Acrylamide (2-Propenamide) is used to manufacture various polymers, especially polyacrylamide.
This water-soluble polymer, which has very low toxicity, is widely used as thickener and flocculating agent.
These functions are valuable in the purification of drinking water, corrosion inhibition, mineral extraction, and paper making.

Acrylamide (2-Propenamide) gels are routinely used in medicine and biochemistry for purification and assays.
Acrylamide (2-Propenamide) is a key monomer used in the production of polyacrylamide, a versatile polymer with wide-ranging applications.
Acrylamide (2-Propenamide) is used as a flocculant in wastewater treatment to help separate solids from water.

Acrylamide (2-Propenamide) is used in the paper industry as a retention and drainage aid.
Acrylamide (2-Propenamide) is utilized in the petroleum industry for EOR processes to increase the yield of oil production.
Acrylamide (2-Propenamide) is used extensively in biochemical and molecular biology laboratories to create polyacrylamide gels for techniques like gel electrophoresis.

These gels are used to separate and analyze DNA, RNA, and proteins.
Acrylamide (2-Propenamide)-based grouts are used in construction and civil engineering to stabilize soil and fill voids or cracks in structures.
Acrylamide (2-Propenamide)-based polymers are employed in the treatment of municipal and industrial wastewater to remove impurities and solids.

Acrylamide (2-Propenamide) and its derivatives are sometimes used in cosmetics and personal care products, particularly hair care products like hair gels and hair sprays.
Acrylamide (2-Propenamide)-based polymers are used in agriculture to improve soil structure and water retention.
Acrylamide (2-Propenamide)-based polymers are used in the textile industry as sizing agents and for improving fabric quality.

Acrylamide (2-Propenamide) is used in the manufacture of adhesives and sealants for various applications.
While not a direct use of Acrylamide (2-Propenamide), it is worth noting that acrylamide can form in some foods during high-temperature cooking processes, such as frying and baking, due to the Maillard reaction.
However, this is an unintentional and potentially undesirable aspect of food preparation.

Acrylamide (2-Propenamide) and its derivatives are also used in research and development for various applications, including materials science and pharmaceuticals.
Acrylamide (2-Propenamide) and its polymer, polyacrylamide, are widely used in water treatment processes as flocculants.
They help to clarify water by causing impurities and solid particles to aggregate and settle, making it easier to separate clean water from contaminants.

This application is crucial for purifying drinking water and treating industrial waste water.
Acrylamide (2-Propenamide) is used in soil erosion control to reduce soil erosion caused by water runoff.
Acrylamide (2-Propenamide) improves soil structure and water infiltration, making it particularly valuable in agriculture, construction, and land reclamation projects.

Acrylamide (2-Propenamide)-based polymers are used in the paper and pulp industry to enhance the retention and drainage properties of paper pulp during the papermaking process.
This helps improve the quality of paper products.
Acrylamide (2-Propenamide)-based polymers are employed in the mining industry for thickening and dewatering processes, which are essential for separating valuable minerals from ore and for waste management.

In addition to enhanced oil recovery (EOR), polyacrylamide is used in oil and gas production as a friction reducer in hydraulic fracturing (fracking) fluids, which are injected into oil and gas reservoirs to enhance production.
Acrylamide (2-Propenamide) is used in gel electrophoresis techniques, such as SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis), which is essential for separating and analyzing proteins and nucleic acids in molecular biology and biochemistry research.

Acrylamide (2-Propenamide)-based polymers are used as soil conditioners in agriculture to improve soil quality, increase water retention, and enhance nutrient uptake by plants.
This can lead to improved crop yields and sustainability.
In the textile industry, acrylamide-based polymers are used for textile sizing and finishing processes.

They can enhance the texture, durability, and appearance of fabrics.
While less common, Acrylamide (2-Propenamide) and its derivatives can be found in some cosmetic and personal care products, such as hair styling products, as binding or thickening agents.
Acrylamide (2-Propenamide) is a key monomer used in the production of polyacrylamide, a polymer with a wide range of applications.

Acrylamide (2-Propenamide) is used in water treatment processes, as a flocculant to clarify water, in the production of paper, and in the petroleum industry for enhanced oil recovery.
Acrylamide (2-Propenamide) is used in biochemical and molecular biology laboratories to create polyacrylamide gels for techniques like gel electrophoresis.
These gels are commonly used to separate and analyze DNA, RNA, and proteins.

Acrylamide (2-Propenamide)-based grouts are used in construction and civil engineering to stabilize soil and fill voids or cracks in structures.
Acrylamide (2-Propenamide)-based polymers are used in wastewater treatment processes to remove impurities and solids from water.

Hazards
Acrylamide (2-Propenamide)is also a skin irritant and may be a tumor initiator in the skin, potentially increasing risk for skin cancer.
Symptoms of acrylamide exposure include dermatitis in the exposed area, and peripheral neuropathy.
Laboratory research has found that some phytochemicals may have the potential to be developed into drugs which could alleviate the toxicity of acrylamide.

The presence of Acrylamide (2-Propenamide) in food has raised health concerns because it has been linked to cancer in laboratory animals when administered at high doses.
However, the risk to humans from dietary exposure to acrylamide is still a subject of ongoing research and debate among scientists and regulatory agencies.

It's important to note that the levels of Acrylamide (2-Propenamide) found in foods are typically much lower than the doses used in animal studies that showed carcinogenic effects.
Additionally, the actual risk to human health from dietary exposure to acrylamide remains uncertain, and it is difficult to establish a clear cause-and-effect relationship between dietary Acrylamide (2-Propenamide) and cancer in humans.

Toxicity and carcinogenicity
Acrylamide (2-Propenamide) can arise in some cooked foods via a series of steps by the reaction of the amino acid asparagine and glucose.
This condensation, one of the Maillard reactions, followed by dehydrogenation produces N-(D-glucos-1-yl)-L-asparagine, which upon pyrolysis generates some Acrylamide (2-Propenamide).

The discovery in 2002 that some cooked foods contain Acrylamide (2-Propenamide) attracted significant attention to its possible biological effects.
IARC, NTP, and the EPA have classified it as a probable carcinogen, although epidemiological studies (as of 2019) suggest that dietary acrylamide consumption does not significantly increase people's risk of developing cancer.

Synonyms
ACRYLAMIDE
79-06-1
2-Propenamide
prop-2-enamide
Propenamide
Ethylenecarboxamide
Acrylic amide
Vinyl amide
Akrylamid
Acrylic acid amide
Acrylagel
Propeneamide
Optimum
2-Propeneamide
9003-05-8
Amresco Acryl-40
Ethylene Carboxamide
Propenoic acid amide
Amid kyseliny akrylove
RCRA waste number U007
Acrylamide Monomer
Akrylamid [Czech]
CCRIS 7
Amide propenoic acid
NSC 7785
Acrylamide-13C3
Acrilamida
Porisutoron
HSDB 191
Amid kyseliny akrylove [Czech]
acryl amide
CHEBI:28619
Flokonit E
Aminogen PA
Acrylamide Monome
Flygtol GB
Stipix AD
EINECS 201-173-7
Superfloc 84
Cytame 5
UNII-20R035KLCI
Sursolan P 5
Solvitose 433
Sumitex A 1
Superfloc 900
Cyanamer P 35
Gelamide 250
Nacolyte 673
Versicol W 11
BRN 0605349
Magnafloc R 292
Sumirez A 17
Sumirez A 27
20R035KLCI
Aerofloc 3453
Cyanamer P 250
Praestol 2800
DTXSID5020027
Himoloc SS 200
Propenoic acid, amide
Stokopol D 2624
ACYLAMIDE-
AI3-04119
Bio-Gel P 2
Reten 420
American Cyanamid KPAM
BioGel P-100
K-PAM
NSC-7785
UN2074
American Cyanamid P-250
RCRA waste no. U007
Dow ET 597
DTXCID6027
Taloflote
Pamid
AAM
Acrylamide, electrophoresis grade
NSC7785
EC 201-173-7
Acrylamide [UN2074] [Poison]
MFCD00008032
Himoloc OK 507
Percol 720
PAARK 123sh
ACRYLAMIDE (IARC)
ACRYLAMIDE [IARC]
ACRYLAMIDE (MART.)
ACRYLAMIDE [MART.]
PAA-1
Dow J 100
PAA 70L
PAM-50
Q 41F
AP 273
ET 597
Acrylamide 1000 microg/mL in Methanol
CAS-79-06-1
J 100
P 250
P 300
acrylarnide
Acrilammide
Crylamide
Amide propenoate
2-propenamida
2-propene amide
acryloic acid amide
1HC
37 - Acrylamide
Acrylamide, 97%
Acrylamide, Inhalable
Bio Gel P2
Bio Gel P-2
Bio-Gel P-2
Acrylamide (Ultrapure)
AAM (CHRIS Code)
ACRYLAMIDE [MI]
CH2CHCONH2
ACRYLAMIDE [HSDB]
ACRYLAMIDE [INCI]
bmse000392
D0L0SP
Acrylamide Solution, 40%
Acrylamide, >=98.0%
Acrylamide, >=99.9%
acrylamide; prop-2-enamide
RCRA Waste Numbrt U007
WLN: ZV1U1
PROPENAMIDE (50%)
Acrylamide_RamanathanGurudeeban
BIDD:ER0629
Acrylamide, analytical standard
CHEMBL348107
GTPL4553
Acrylamide, for synthesis, 99%
Acrylamide [UN2074] [Poison]
USEPA Pesticide Code: 600008
BCP25183
Tox21_201526
Tox21_300145
BDBM50226193
NA2074
NSC116573
NSC116574
NSC116575
NSC118185
STL282727
UN3426
788 - Acrylamide analysis in snacks
881 - Acrylamide analysis in coffee
AKOS000120965
Ethylene monoclinic tablets carboxamide
Acrylamide, purum, >=98.0% (GC)
LS-1769
NSC-116573
NSC-116574
NSC-116575
NSC-118185
UN 2074
Acrylamide Monomer (ca. 50% in Water)
Acrylamide Monomer [for Electrophoresis]
NCGC00090736-01
NCGC00090736-02
NCGC00090736-03
NCGC00090736-04
NCGC00090736-05
NCGC00253932-01
NCGC00259076-01
Acrylamide Monomer, [for Electrophoresis]
Acrylamide, SAJ first grade, >=98.0%
A0139
A1132
Acrylamide, Ultrapure, Electrophoresis Grade
FT-0661414
FT-0688081
EN300-20803
C01659
Acrylamide, suitable for electrophoresis, >=99%
A839565
Acrylamide, for electrophoresis, >=99.0% (GC)
Q342939
Acrylamide, for molecular biology, >=99% (HPLC)
J-200356
J-510287
Acrylamide, certified reference material, TraceCERT(R)
Acrylamide, for electrophoresis, >=99% (HPLC), powder
BC269F2E-D242-48E1-87E4-E51DB86FF0A8
F8880-6341
InChI=1/C3H5NO/c1-2-3(4)5/h2H,1H2,(H2,4,5
Acrylamide, for Northern and Southern blotting, powder blend
Acrylamide, Vetec(TM) reagent grade, suitable for electrophoresis
HJ 801-2016 SVOC Mixture 492 500-1000 microg/mL in Water
ACRYLAMIDO-2-METHYL-1-PROPANE SULFONIC ACID (AMPS)

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is a white to off-white crystalline powder.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) has the chemical formula C7H13NO4S and a molecular weight of 207.25 g/mol.

CAS Number: 15214-89-8
EC Number: 239-268-0

Synonyms: 2-Acrylamido-2-methylpropane sulfonic acid, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS), Acrylamido-2-methylpropylsulfonic acid, 2-Acrylamido-2-methyl-1-propane sulfonic acid, 2-Propenamide, 2-methyl-2-(sulfooxy)-, 2-Propenamide, 2-methyl-2-propanesulfonic acid, 2-Methyl-2-propenoylaminopropanesulfonic acid, Acrylamido-2-methylpropanesulfonic acid, 2-Acrylamido-2-methylpropanesulfonic acid, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)A, 2-Acrylamido-2-methyl-1-propanesulfonic acid, N-(1,1-Dimethyl-2-propenyl)sulfonamide, 2-Acrylamido-2-methylpropyl sulfonic acid, N-(1,1-Dimethyl-2-propenyl)sulfonic acid, 2-Propenamide, N-(2-sulfoethyl)-, 2-Propenamide, 2-methyl-2-propanesulfonic acid, N-[2-(Methylsulfonyl)ethyl]acrylamide, 2-Acrylamido-2-methyl-1-propanesulphonic acid, Acrylamide, 2-methyl-2-propanesulfonic acid, N-(2-Sulfoethyl)acrylamide, 2-Propenamide, 2-methyl-N-(2-sulfoethyl)-, Acrylamide, 2-methyl-2-propanesulfonic acid, Acrylamide, N-(1,1-dimethyl-2-propenyl)sulfonic acid, 2-Acrylamido-2-methylpropylsulfonic acid, 2-Propenamide, N-(2-sulfoethyl)-2-methyl-, 2-Acrylamido-2-methylpropylsulfonic acid, Acrylamide, N-(1,1-dimethyl-2-propenyl)sulfonic acid, Acrylamido-2-methyl-1-propane sulfonic acid, 2-Propenamide, 2-methyl-N-(2-sulfoethyl)-, N-(1,1-Dimethyl-2-propenyl)sulfonamide, 2-Methyl-2-propenoylaminopropanesulfonic acid, Acrylamido-2-methylpropanesulfonic acid, N-(1,1-Dimethyl-2-propenyl)sulfonic acid, 2-Propenamide, N-(2-sulfoethyl)-, 2-Propenamide, 2-methyl-2-propanesulfonic acid, 2-Propenamide, N-(2-sulfoethyl)-2-methyl-, Acrylamido-2-methyl-1-propanesulphonic acid, 2-Acrylamido-2-methylpropyl sulfonic acid, 2-Acrylamido-2-methylpropylsulfonic acid, Acrylamido-2-methyl-1-propane sulfonic acid, 2-Propenamide, 2-methyl-N-(2-sulfoethyl)-, N-[2-(Methylsulfonyl)ethyl]acrylamide, 2-Propenamide, N-(2-sulfoethyl)-2-methyl-, Acrylamido-2-methyl-1-propanesulphonic acid, Acrylamide, 2-methyl-2-propanesulfonic acid, 2-Methyl-2-propenoylaminopropanesulfonic acid, Acrylamide, N-(1,1-dimethyl-2-propenyl)sulfonic acid, N-(1,1-Dimethyl-2-propenyl)sulfonamide, 2-Acrylamido-2-methylpropyl sulfonic acid, 2-Acrylamido-2-methylpropylsulfonic acid, N-(2-Sulfoethyl)acrylamide, Acrylamido-2-methyl-1-propane sulfonic acid



APPLICATIONS


Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in water treatment chemicals to prevent scale formation and corrosion in industrial water systems.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) serves as a monomer in the production of superabsorbent polymers for hygiene products such as diapers and adult incontinence pads.
In the oil and gas industry, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is an essential additive in drilling fluids, enhancing their thermal stability and salt tolerance.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in cement and concrete admixtures to improve water retention, workability, and mechanical strength.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is a key ingredient in water-soluble polymers used as thickeners, dispersants, and stabilizers.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in textile processing to improve dye uptake and provide antistatic properties to fibers.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the performance of paper products by serving as a retention aid and strength enhancer in paper manufacturing.

In personal care products, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) acts as a rheology modifier and conditioning agent in shampoos, creams, and lotions.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based polymers are used as dispersants in pigment and dye formulations to ensure uniform color distribution.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in water-based paints and coatings to improve adhesion, flexibility, and resistance to environmental factors.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is a crucial component in the formulation of pressure-sensitive adhesives, providing enhanced tack and adhesion.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in superplasticizers for concrete to increase flowability without adding extra water.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is incorporated into hydrogel formulations for medical and pharmaceutical applications, including wound dressings.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the production of ion-exchange resins for water purification and softening processes.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) improves the thermal and oxidative stability of polymers used in high-temperature applications.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the formulation of emulsifiers and dispersants for agricultural chemicals, ensuring stable mixtures.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the performance of lubricants and greases by providing corrosion inhibition and stability.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the production of synthetic rubber and elastomers, improving their processability and performance.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based copolymers are utilized in waterborne adhesives for packaging and woodworking applications.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) serves as a functional monomer in the synthesis of specialty polymers with specific properties, such as conductivity and bio-compatibility.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the formulation of anti-scaling agents for desalination plants and cooling towers.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is a key ingredient in the manufacture of flocculants for wastewater treatment, aiding in the removal of suspended solids.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the production of coatings for electronic devices, providing moisture resistance and durability.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the formulation of printing inks to improve viscosity and stability.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the performance of sealants and caulks used in construction, providing better adhesion and flexibility.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in detergents and cleaning products to enhance their efficiency by acting as a dispersant and anti-redeposition agent.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is utilized in the manufacturing of contact lenses, where it helps to maintain moisture and comfort.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is an important component in the formulation of hydraulic fracturing fluids, aiding in the extraction of oil and gas.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in hair styling gels and mousses to provide hold and conditioning properties.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is employed in the production of coatings for food packaging, improving barrier properties and durability.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in agricultural formulations as a soil conditioner to improve water retention and nutrient availability.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is included in the formulation of antifreeze and coolant additives to prevent corrosion and scaling.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the cosmetics industry for its film-forming and moisture-retaining properties.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based polymers are used as thickeners in latex paints, providing better application properties and finish.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the treatment of industrial wastewater to remove heavy metals and organic contaminants.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is incorporated into water-based inks to improve print quality and stability on various substrates.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the formulation of fire retardant coatings, enhancing their effectiveness and durability.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the mining industry to improve the efficiency of ore flotation processes.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is utilized in the production of gel electrolytes for batteries, enhancing ionic conductivity and stability.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the synthesis of hydrophilic membranes for filtration and separation processes.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is included in pharmaceutical formulations to control drug release and improve bioavailability.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based polymers are used in the production of medical adhesives, providing strong and flexible bonds.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is employed in the formulation of rust inhibitors for metal protection in various industrial applications.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the manufacturing of specialty papers, such as photographic and printing papers, to improve quality and performance.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is utilized in the formulation of lubricants for wire drawing and metalworking processes.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the production of waterproofing agents for textiles, providing durability and protection.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is included in the formulation of construction materials, such as grouts and sealants, to improve adhesion and flexibility.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based polymers are used in the production of automotive coatings, providing durability and resistance to environmental factors.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the formulation of industrial cleaners, enhancing their effectiveness in removing stubborn contaminants.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is utilized in the development of advanced materials for biomedical applications, such as drug delivery systems and tissue engineering scaffolds.



DESCRIPTION


Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is a white to off-white crystalline powder.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) has the chemical formula C7H13NO4S and a molecular weight of 207.25 g/mol.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is known for its high water solubility, making it suitable for aqueous formulations.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is commonly used as a monomer in polymer synthesis.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is widely utilized in the water treatment industry for its scale inhibition properties.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) exhibits excellent thermal and hydrolytic stability.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) can copolymerize with a wide range of vinyl monomers.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is often used to modify the properties of synthetic and natural polymers.
In the oil and gas industry, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is an essential additive in drilling fluids and enhanced oil recovery.

The presence of a sulfonic acid group in Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) provides high ionic character and hydrophilicity.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is effective in preventing the formation of calcium sulfate and calcium carbonate scales.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the water retention properties of concrete admixtures.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the textile industry to improve the dyeability of fabrics.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) provides antistatic properties to textile fibers.

In personal care products, Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) functions as a thickener and conditioning agent.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in superabsorbent polymers for hygiene products like diapers.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) improves the mechanical properties of polymeric materials.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the performance of water-based adhesives and sealants.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS)-based polymers are used as dispersants in various industrial applications.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) contributes to the thermal stability of polymeric materials used in high-temperature environments.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is effective in stabilizing suspensions and emulsions.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is used in the paper industry to improve paper strength and quality.

Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) can form hydrogels with high water absorption capacity.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is utilized in the formulation of coatings and paints for improved adhesion and durability.
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) enhances the performance and stability of chemical formulations in diverse applications.



PROPERTIES


Appearance: White to off-white crystalline powder
Molecular Formula: C7H13NO4S
Molecular Weight: 207.25 g/mol
Melting Point: Approximately 190-195°C (with decomposition)
Boiling Point: Decomposes before boiling
Density: 1.35 g/cm³
Solubility in Water: Highly soluble
Solubility in Other Solvents: Sparingly soluble in ethanol; insoluble in most organic solvents
pH (in solution): Typically acidic
Odor: Odorless
Hygroscopic: Yes



FIRST AID


Inhalation:

Immediate Steps:
Move the affected person to fresh air immediately.
Ensure that they are in a comfortable position for breathing.

Breathing Support:
If the person is having difficulty breathing, provide oxygen if available and if trained to do so.

Symptoms Monitoring:
Keep an eye out for symptoms such as coughing, shortness of breath, or wheezing.
If these symptoms persist or worsen, seek medical attention immediately.

Emergency Action:
If the person is not breathing, begin CPR (cardiopulmonary resuscitation) and call for emergency medical services.


Skin Contact:

Immediate Steps:
Remove any contaminated clothing and accessories immediately to prevent further exposure.

Washing:
Rinse the affected skin area thoroughly with plenty of water for at least 15 minutes.
Use soap if available to ensure complete removal of the chemical.

Symptoms Monitoring:
Look for signs of skin irritation, such as redness, itching, or a rash.
If irritation persists or develops, seek medical advice.

Clothing Handling:
Wash contaminated clothing before reuse to prevent any further contact.


Eye Contact:

Immediate Steps:
Flush eyes immediately with plenty of lukewarm water for at least 15 minutes.
Keep the eyelids open and move the eyeball in all directions to ensure thorough rinsing.

Emergency Action:
Remove contact lenses if present and easy to do.
Continue rinsing.

Symptoms Monitoring:
Watch for signs of irritation such as redness, pain, swelling, or blurred vision.
If any of these symptoms persist, seek medical attention immediately.

Aftercare:
Even if no symptoms are present, it is advisable to get medical evaluation to ensure no damage has occurred to the eyes.


Ingestion:

Immediate Steps:
Do not induce vomiting unless instructed to do so by medical personnel.

Mouth Rinse:
Rinse the mouth thoroughly with water.

Medical Attention:
Seek medical attention immediately, even if no symptoms are present.

Symptoms Monitoring:
Look for signs of gastrointestinal discomfort, such as nausea, vomiting, abdominal pain, or diarrhea.
Provide the medical team with information on the chemical ingested.


HANDLING AND STORAGE

Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE including gloves, safety goggles, lab coat, and, if necessary, respiratory protection.
Ensure that PPE is made of materials resistant to chemicals, and inspect regularly for wear and tear.

General Handling Precautions:
Handle in a well-ventilated area or under an exhaust hood to minimize inhalation exposure.
Avoid contact with skin, eyes, and clothing. Wash hands and face thoroughly after handling.
Do not eat, drink, or smoke in areas where Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is handled or stored.

Spill and Leak Procedures:
In case of a small spill, use appropriate absorbent material and dispose of it according to local regulations.
For larger spills, evacuate the area and follow emergency procedures. Use appropriate containment to prevent environmental contamination.

Safe Work Practices:
Use chemical fume hoods or appropriate local exhaust ventilation to prevent exposure to vapors and dust.
Ensure all containers are properly labeled with the chemical name and hazard warnings.

Equipment and Tools:
Use tools and equipment made from materials compatible with Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) to avoid chemical reactions.
Regularly inspect and maintain equipment to ensure proper functioning and safety.

Training and Documentation:
Ensure that all personnel handling Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) are trained in proper handling techniques, emergency procedures, and use of PPE.
Maintain safety data sheets (SDS) and make them accessible to all personnel.


Storage:

Storage Area Requirements:
Store Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials.
Designate a specific storage area for Acrylamido-2-methyl-1-propane sulfonic acid (AMPS), clearly labeled and restricted to authorized personnel only.

Container Specifications:
Use containers made of compatible materials such as polyethylene or glass. Ensure they are tightly sealed to prevent moisture ingress.
Regularly inspect storage containers for signs of damage or leaks.

Temperature Control:
Store Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) at temperatures between 10-25°C (50-77°F) to prevent degradation.
Avoid exposure to extreme temperatures which can lead to decomposition or altered chemical properties.

Humidity and Moisture Control:
Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is hygroscopic and should be kept in a low-humidity environment.
Use desiccants in storage areas to control moisture levels.

Segregation:
Store Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) away from incompatible substances such as strong oxidizing agents, acids, and bases to prevent chemical reactions.
Ensure physical segregation from food, beverages, and animal feed to avoid contamination.

Fire Protection:
Although Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) is not highly flammable, it is important to store it away from ignition sources.
Equip storage areas with appropriate fire extinguishing systems and keep emergency contact numbers readily accessible.

Labeling and Documentation:
Clearly label all storage containers with the chemical name, CAS number, and hazard warnings.
Keep an inventory log of stored chemicals and regularly update it to track usage and storage conditions.

Emergency Procedures:
Establish and clearly post emergency procedures for spills, leaks, and other accidental releases.
Ensure that emergency showers and eyewash stations are readily accessible in storage and handling areas.

Inspection and Maintenance:
Conduct regular inspections of storage areas to ensure compliance with safety regulations and to identify potential hazards.
Maintain records of inspections, maintenance, and any incidents for continuous safety improvement.

Disposal Considerations:
Dispose of Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) according to local, state, and federal regulations. Consult the SDS for specific disposal recommendations.
Do not dispose of Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) in regular trash or down the drain. Use certified waste disposal companies for hazardous chemicals.
ACRYLAMIDOPROPYLTRIMONIUM CHLORIDE/ACRYLAMIDE
acrylamide; Acrylic amide; Ethylene Carboxamide; 2-Propenamide; Propenoic acid, amide; Vinyl Amide; cas no: 79-06-1
Acrylamide (powder)
Ethylic acid; Methanecarboxylic acid; vinegar; Vinegar acid; Acetic acid, glacial; Essigsäure; ácido acético; Acide acétique; Ethanoic acid; Acetasol; Octowy kwas; Kyselina octova; Essigsaeure; Octowy kwas; Vosol; CHLORINE IODIDE; CHLOROIODIDE; IODINE CHLORIDE; IODINE MONOCHLORIDE; IODINE MONOCHLORIDE SOLUTION, WIJS; IODINE-MONOCHLORIDE, WIJS; IODINE SOLUTION ACCORDING TO WIJS; IODOCHLORIDE; IODOMONOCHLORIDE; WIJS CHLORIDE; WIJS' CHLORIDE; WIJS IODINE SOLUTION; WIJ'S IODINE SOLUTION; WIJS REAGENT; WIJS' REAGENT; WIJS SOLUTION; WIJS' SOLUTION; Acetasol; aceticacid(non-specificname); aceticacid(solutionsgreaterthan10%) CAS NO:64-19-7, 77671-22-8
Acrylamido tert-Butyl Sulfonic acid
SYNONYMS Ethylic acid; Methanecarboxylic acid; vinegar; Vinegar acid; Acetic acid, glacial; CAS NO. 64-19-7, 77671-22-8
ACRYLATES COPOLYMER
Acroleic acid; 2-Propenoic acid; Acrylate; Ethylenecarboxylic acid; propene acid; Propenoic acid; Vinylformic Acid; Acide acrylique; Acido acrilio; Kyselina akrylova; 2-PROPENOIC ACID; Acroleic acid; ACRYLIC ACID; AKOS BBS-00003787; ETHYLENECARBOXYLIC ACID; PROPENOIC ACID; RARECHEM AL BO 0141; 2-Propensαure; acideacrylique; acideacrylique(french); acidoacrilio; Acrylate; acrylicacid,[waste]; acrylicacid,glacial; acrylicacid,inhibited; Acrylsαure; ai3-15717; caswellno.009a; CH2=CHCOOH; Glacial acrylic acid CAS NO: 79-10-7
ACRYLIC ACID GLACIAL (GAA)
Acrylic Acid Glacial (GAA)’s molecular formula is C3H4O2.
Acrylic Acid Glacial (GAA) is a clear, colorless liquid with a characteristic acrid odor.
Acrylic Acid Glacial (GAA) has a role as a metabolite.


CAS Number: 79-10-7
EC Number: 201-177-9
Chemical formula: C3H4O2



SYNONYMS:
GAA, ACRYLIC ACID, 2-Propenoic acid, 79-10-7, Propenoic acid, prop-2-enoic acid, Vinylformic acid, Acroleic acid, Propene acid, Ethylenecarboxylic acid, Acrylic Acid, Acroleic acid, Propenoic acid, Vinylformic acid, 2-Propenoic acid, Refined Acrylic Acid, High Purity Acrylic Acid, GAA, Glacial Acrylic Acid, 2-Propenoic acid, vinyl formic acid, Ethylenecarboxylic acid, Methacrylic Acid, 2-Propenoic acid, 2-methyl-, a-Methylacrylic Acid



Acrylic Acid Glacial (GAA) is a clear, colorless liquid with a characteristic acrid odor.
Acrylic Acid Glacial (GAA) is miscible with water, alcohols and ethers.
Acrylic Acid Glacial (GAA) will undergo the typical reactions of a carboxylic acid, as well as reactions of the double bond similar to those of the acrylate esters.


Acrylic Acid Glacial (GAA) lends itself to polymer preparation as well as use as a chemical intermediate.
Acrylate esters, both mono- and multifunctional, are generally prepared from acrylic acid.
Acrylic Acid Glacial (GAA) is a clear, colorless liquid with a characteristic acrid odor.


Acrylic Acid Glacial (GAA) is miscible with water, soluble in most organic solvents and has relatively low volatility.
Acrylic Acid Glacial (GAA), appears as a colorless liquid with a distinctive acrid odor.
Acrylic Acid Glacial (GAA) is a colorless liquid with a distinctive acrid odor.


Flash point of Acrylic Acid Glacial (GAA) is 130°F.
Acrylic Acid Glacial (GAA) is a alpha,beta-unsaturated monocarboxylic acid that is ethene substituted by a carboxy group.
Acrylic Acid Glacial (GAA) has a role as a metabolite.


Acrylic Acid Glacial (GAA) is a clear, colourless liquid with an acrid odour which is miscible with water, alcohols and ethers.
Acrylic Acid Glacial (GAA) is an unsaturated monocarboxylic acid which will undergo the typical reactions of a carboxylic acid as well as those of a vinyl compound.


Acrylic Acid Glacial (GAA) is the simplest carboxylic acid and a precursor for many other acrylates, acrylic polymers, and co-polymers.
Acrylic Acid Glacial (GAA) is the basic building block for all acrylic chemistry.
Acrylic Acid Glacial (GAA) is an unsaturated monocarboxylic acid.


Acrylic Acid Glacial (GAA) is an effective as a vinyl compound and as a carboxylic acid.
Acrylic Acid Glacial (GAA) is easily subjected to radial (co)polymerization and addition reactions.
Copolymers of Acrylic Acid Glacial (GAA) can be prepared with (meth)acrylic esters, acrylonitrile, vinyl acetate, vinyl chloride, styrene, and other monomers by all known radical polymerization technologies.


Acrylic Acid Glacial (GAA) is an unsaturated monocarboxylic acid monomer which is a clear, colourless liquid with an acrid odour which is miscible with water, alcohols and ethers.
Acrylic Acid Glacial (GAA)’s molecular formula is C3H4O2.


Acrylic Acid Glacial (GAA) is a highly pure acrylic acid used for an organic synthesis and polyelectrolyte.
Acrylic Acid Glacial (GAA) contains 220 ppm MEHQ inhibitor.
Acrylic Acid Glacial (GAA) is an unsaturated carboxylic acid available in the form of clear colorless liquid with a characteristic acrid odor.


Acrylic Acid Glacial (GAA) is miscible with water, alcohols and ethers.
Acrylic Acid Glacial (GAA) is undergone the typical reactions of a carboxylic acid, as well as reactions of the double bond similar to those of the acrylate esters.


Acrylic Acid Glacial (GAA) is used for polymer preparation and as a chemical intermediate.
Acrylate esters are generally prepared from acrylic acid.
Acrylic Acid Glacial (GAA) is a clear, colorless liquid with a characteristic acrid odor.


Acrylic Acid Glacial (GAA) is miscible with water, alcohols and ethers.
Acrylic Acid Glacial (GAA) will undergo the typical reactions of a carboxylic acid, as well as reactions of the double bond similar to those of the acrylate esters.


Acrylic Acid Glacial (GAA) lends itself to polymer preparation as well as use as a chemical intermediate.
Acrylate esters, both mono- and multifunctional, are generally prepared from acrylic acid.
Acrylic Acid Glacial (GAA) is an unsaturated carboxylic acid co-monomer used in a wide range of copolymers.


Acrylic Acid Glacial (GAA) readily copolymerizes with acrylic and methacrylic esters, ethylene, vinyl acetate, styrene, butadiene, acrylonitrile, maleic acid esters, vinyl chloride and vinylidene chloride.
Copolymers which contain Acrylic Acid Glacial (GAA) can be solubilized or exhibit improved dispersed in water; the carboxylic acid moiety can be used for coupling or crosslinking reactions.


Acrylic Acid Glacial (GAA) is a clear, colorless liquid with a pungent, acrid odor.
Acrylic Acid Glacial (GAA)'s comprised of a polymerizable vinyl functional group on one end and a reactive acid group on the other end.
Acrylic Acid Glacial (GAA) is miscible with water, soluble in most organic solvents and has relatively low volatility.


Acrylic Acid Glacial (GAA)'s vapor is heavier than air.
Acrylic Acid Glacial (GAA) copolymerizes readily with a wide variety of monomers.
The added acid group imparts properties such as durability, strength, adhesion and an elevated Tg.


Applications Acrylic Acid Glacial (GAA) can be homopolymerized into polyacrylic acid which is used in super absorbent
polymers (SAPs), ion exchange resins and detergents.
Acrylic Acid Glacial (GAA) can be co-polymerized with a variety of other monomers such as MMA, EHA, VAM, styrene and vinyl chloride.
These products exhibit good weather ability, flexibility, hardness and abrasion resistance.



USES and APPLICATIONS of ACRYLIC ACID GLACIAL (GAA):
Acrylic Acid Glacial (GAA) is used copolymer-based finishes, coatings, adhesives, inks, lubricants, saturants, and plastics.
Acrylic Acid Glacial (GAA) is also used in the production of a wide variety of specialty esters, in drilling fluids and mineral processing chemicals, detergent builders, water treatment chemicals and in superabsorbent materials.


Acrylic Acid Glacial (GAA) is used Polymer, Chemical Intermediate
Recommended Use of Acrylic Acid Glacial (GAA): Paints and Coatings, Adhesives, Detergents, Water Treatment, Super Absorbent Polymers (SAPs), Enhanced Oil Recovery, and Floor polishes.


Acrylic Acid Glacial (GAA) is also used in the manufacture of paints, coatings, adhesives and binders, detergents, diapers and floor polishes as well as finding use in a variety of medical applications.
Acrylic Acid Glacial (GAA) is widely used in super absorbent polymer, addition polymerization of macromolecular and monomer for polyelectrolyte, organic synthesis, water treatment reagent and paper-making chemicals as functional monomer.


Acrylic Acid Glacial (GAA) is a chemical which is typically polymerized to give mechanical structure emulsions and resins.
Acrylic Acid Glacial (GAA) is used as raw material for specialty acrylates.
Recommended for application of Acrylic Acid Glacial (GAA) in production of impregnating materials and adhesives.


Acrylic Acid Glacial (GAA) is used in the production of polymers and acrylate esters and as a feedstock for chemical syntheses.
Acrylic Acid Glacial (GAA) is used in coatings, adhesives, solid resins, molding compounds.
Acrylic Acid Glacial (GAA) has useful properties such as flexibility, good weathering, adhesion, hardness and resistance to abrasion and oils and as such it is used as an additive in a wide range of products.


Acrylic Acid Glacial (GAA) is used as an additive in a variety of copolymer-based finishes, coatings, adhesives, inks, lubricants, saturants, and plastics.
Acrylic Acid Glacial (GAA) is also used in a range of esters for specialist applications such as in water treatment chemicals, drilling fluids, mineral processing chemicals,detergent builders andsuperabsorbents.


As a superabsorbent polymer (SAP), Acrylic Acid Glacial (GAA) is used in the production of nappies and other sanitary products.
Acrylic Acid Glacial (GAA) can also be copolymerised with acrylamides, which act as a flocculant in water purification.
Acrylic Acid Glacial (GAA) is a water free version of acrylic acid.


Acrylic Acid Glacial (GAA) and the its acrylates are used as the components for polymers used in adhesives, coatings, inks, plastics, elastomers, water treatment, personal care, and various other industries.
Key Applications of Acrylic Acid Glacial (GAA): Paints; Coatings; Adhesives; Construction; Detergents;Personal care; Leather treatments; Textile chemicals; Acrylic resin manufacture; Water treatment.


Acrylic Acid Glacial (GAA) is commonly used in a number of end products such as textile, leather and paper finishes, floor polish, plastics, scale inhibitors, hair styling and finishing products, paints, lacquers, adhesives, vehicle paint, dispersants, saturants and thickeners.
Acrylic Acid Glacial (GAA) is used to produce various esters from esterification reactions with alcohol.


Polyacrylic acid and copolymers of Acrylic Acid Glacial (GAA) are used in the pulp and paper, paint and varnish, textile industries, the production of detergents, ceramics, perfumes, and cosmetics, in water treatment, in medicine and oil production as binders, film-forming agents, thickeners, scale inhibitors, adhesives, drilling mud modifiers, modifiers drugs, etc.


The scope of their application of Acrylic Acid Glacial (GAA) is constantly expanding.
Acrylic Acid Glacial (GAA) is used to synthesize its esters and salts.
Acrylic Acid Glacial (GAA) is used in the production of superabsorbent.


Acrylic Acid Glacial (GAA) is applied in the production of: Acrylic & Waterborne dispersions, Industrial & Architectural coatings, Paints & Varnishes, Textiles, Pulp & Paper, Paper & Leather coatings, Wood & Metal coatings, Film-forming agents, Thickeners, Scale inhibitors, Adhesives, Drilling mud modifiers, Inks, caulks & sealants, and Many of the other industries…


Acrylic Acid Glacial (GAA) has useful properties such as flexibility, good weathering, adhesion, hardness and resistance to abrasion and oils and as such it is used as an additive in a wide range of products.
Acrylic Acid Glacial (GAA) readily copolymerizes with acrylic and methacrylic esters, ethylene, vinyl acetate, styrene, butadiene, acrylonitrile, maleic esters, vinyl chloride and vinylidene chloride.


Acrylic Acid Glacial (GAA) has 2 main application, for the polymeric application and for the manufacture of acrylate esters.
Acrylic Acid Glacial (GAA) is commonly used as an additive in a variety of copolymer-based finishes, coatings, adhesives, inks, lubricants, textile, leather, paper finishes, floor polish, plastics, scale inhibitors, hair styling and finishing products, paints, lacquers, plastics, adhesives, dispersants, and thickeners.


Acrylic Acid Glacial (GAA) is also used in a range of esters for specialist applications such as in water treatment chemicals when it’s copolymerised with acrylamides, in drilling fluids, in mineral processing chemicals, detergent builders and in super absorbents polymers (SAP) for the production of nappies and sanitary products.


Acrylic Acid Glacial (GAA) is used Super Absorbent Polymers, Water Treatment, Enhanced Oil Recovery, Paints and Coatings, Adhesives, and Detergents.
Acrylic Acid Glacial (GAA) copolymers can be used in the form of their free acids, ammonium salts or alkali salts in applications such as thickeners, dispersing agents, flocculants, protective colloids and polymer dispersions, wetting agents, coatings, adhesives, inks and textile finishes.


Acrylic Acid Glacial (GAA) is used in industries of a super absorbent polymer, and an addition polymerization of macromolecule.
Acrylic Acid Glacial (GAA) is also used in a wide variety of specialty copolymers in drilling fluids and mineral processing chemicals, water treatment polymers and superabsorbent materials.



BENEFITS OF ACRYLIC ACID GLACIAL (GAA):
*Weather moisture and abrasion resistance
*Impact strength flexibility durability and toughness
*Dry adhesion



SUGGESTED INDUSTRIES OF ACRYLIC ACID GLACIAL (GAA):
*Adhesives & Sealants,
*Plastics & Packaging,
*Coatings & Paints,
*Construction & Building Materials



IMPORTANT PROPERTIES OF ACRYLIC ACID GLACIAL (GAA):
The resulting polymer chains bear functional groups that impart the following important properties to the polymer products;
• Impact strength, flexibility, durability, toughness
• Weather resistance, moisture resistance
• Crosslinking sites, acid group reacts readily with alcohols, acrylates and styrenics.
• Hardness, wet and dry adhesion and abrasion resistance are also properties of GAA copolymers.
• Acrylic Acid Glacial (GAA) is also used in the manufacture of paints, coatings, adhesives and binders, detergents, diapers and floor polishes as well as finding use in a variety of medical applications.



SYNTHESIS SOLUTIONS OF ACRYLIC ACID GLACIAL (GAA):
Acrylic Acid Glacial (GAA) and its esters undergo the reactions of the double bond which readily combine with themselves or other monomers (e.g. amides, methacrylates, acrylonitrile, vinyl, styrene and butadiene) to form homopolymers or co-polymers which are used in the production of coatings, adhesives, elastomers, super absorbent polymers, flocculants, as well as fibers and plastics.
Acrylate polymers show a wide range of properties dependent on the type of the monomers and reaction conditions.



BENEFITS OF ACRYLIC ACID GLACIAL (GAA):
*Impact strength, flexibility, durability, toughness
*Weather resistance, moisture resistance
*Crosslinking sites, acid group reacts readily with alcohols, acrylates and styrenics
*Hardness, wet and dry adhesion and abrasion resistance are also properties of GAA copolymers



PRODUCTION OF ACRYLIC ACID GLACIAL (GAA):
Acrylic Acid Glacial (GAA) is synthesized by the oxidation of propene via acrolein.



ACRYLIC ACID GLACIAL (GAA) MARKET OVERVIEW:
The Acrylic Acid Glacial (GAA) Market size is expected to develop revenue and exponential market growth at a remarkable CAGR during the forecast period from 2023–2030.

The growth of the market can be attributed to the increasing demand for Acrylic Acid Glacial (GAA) owning to the Paints and Coatings, Textile Industry, Water Treatment Agent, Pulp and Paper, Petroleum, Other Applications across the global level.
The report provides insights regarding the lucrative opportunities in the Acrylic Acid Glacial (GAA) Market at the country level.

The report also includes a precise cost, segments, trends, region, and commercial development of the major key players globally for the projected period.
The Acrylic Acid Glacial (GAA) Market report represents gathered information about a market within an industry or various industries.

The Acrylic Acid Glacial (GAA) Market report includes analysis in terms of both quantitative and qualitative data with a forecast period of the report extending from 2023 to 2030.



FEATURES AND BENEFITS OF ACRYLIC ACID GLACIAL (GAA):
*Hydrophilicity
*Water solubility
*Adhesion
*Any required rheological properties



STORAGE AND HANDLING OF ACRYLIC ACID GLACIAL (GAA):
Acrylic Acid Glacial (GAA) polymerizes readily and is therefore supplied in stabilised form.
Acrylic Acid Glacial (GAA) must be stored under air rather than inert gases to prevent spontaneous polymerization.
Storage Acrylic Acid Glacial (GAA) temperature must be between 15°C and 25°C.
Provided these storage conditions are properly maintained, the product can be expected to remain stable for a period of one year.



PHYSICAL and CHEMICAL PROPERTIES of ACRYLIC ACID GLACIAL (GAA):
Formula weight: 72.06 g/mol
Appearance: Clear, colorless liquid
Odor: Pungent, acrid
Specific gravity at 20°C: 1.051
Refractive index at 25°C: 1.415
Viscosity, cps at 20°C: 1.3
Boiling point at 760 mmHg: 141°C
Freezing point: 14°C
Solubility in water: Miscible
Tg of homopolymer: 87°C

Molecular weight: 72.06 g/mol
Appearance: Colorless liquid
Density: 1.05 g/cm³
Refractive index: 1.4224
Color: 20 Max.
Assay: 99.5% Min
Water content: 0.2% Max.
Inhibitor (MEHQ): 200 +/- 20 ppm
Odor: Acrid odor
Boiling point: 141°C
Melting point: 13°C
Flash point: 46°C



FIRST AID MEASURES of ACRYLIC ACID GLACIAL (GAA):
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ACRYLIC ACID GLACIAL (GAA):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ACRYLIC ACID GLACIAL (GAA):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ACRYLIC ACID GLACIAL (GAA):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ACRYLIC ACID GLACIAL (GAA):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ACRYLIC ACID GLACIAL (GAA):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


acrylic acid
acrylic acid-hydroxypropyl acrylate copolymer ACRYLIC ACID-2-HYDROXYPROPYL ACRYLATE COPOLYMER AcrylicAcid-2-HydroxypropylAcrylateCopolymer(equaltoT-225) Acrylic Acid-2-Hydroxypropyl Acrylate Copolymer (T-225) T-225 Acrylic acid-hydroxypropyl acrylate polymer Acrylic Acid-2-Hydroxypropyl Acrylate Copolymer T-225 or AA/HPA flocculant TS-609 cas :55719-33-0
ACTIPONE ALPHA PULP

Actipone Alpha Pulp is a high-quality natural extract derived from the pulp of apples, known for its potent antioxidant and skin-soothing properties.
Actipone Alpha Pulp is widely used in personal care formulations due to its ability to improve skin hydration, enhance radiance, and protect the skin from oxidative stress.
This versatile ingredient is ideal for a wide range of applications, including anti-aging products, moisturizers, and skin-brightening treatments.

CAS Number: Not specifically assigned (relevant CAS numbers may vary depending on specific components like polyphenols, vitamin C, etc.)
EC Number: Not specifically assigned (relevant EC numbers may vary depending on specific components)

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Actipone Alpha Pulp is applied in the creation of baby care products, offering gentle hydration and protection for delicate skin.
Actipone Alpha Pulp is utilized in the development of anti-pollution skincare products, providing a barrier against environmental pollutants and free radicals.

Actipone Alpha Pulp is found in the formulation of multipurpose balms, offering hydration, protection, and antioxidant benefits for use on lips, face, and body.
Actipone Alpha Pulp is used in the production of night creams, where it supports the skin's natural repair processes and enhances overnight hydration.
Actipone Alpha Pulp is a key ingredient in the creation of exfoliating products, providing gentle exfoliation with added skin conditioning and antioxidant protection.

Actipone Alpha Pulp is widely used in the formulation of toner products, offering hydration and antioxidant benefits that prepare the skin for subsequent skincare steps.
Actipone Alpha Pulp is employed in the development of face oils, providing a nourishing and protective layer that locks in moisture and enhances skin radiance.
Actipone Alpha Pulp is applied in the production of moisturizing sprays, offering a lightweight and refreshing boost of hydration and antioxidants.

Actipone Alpha Pulp is utilized in the creation of body butters, providing rich hydration and antioxidant protection for dry and rough skin.
Actipone Alpha Pulp is found in the formulation of hair masks, offering deep conditioning and protection against oxidative stress for healthier, shinier hair.
Actipone Alpha Pulp is used in the production of anti-aging hand treatments, helping to reduce the appearance of age spots and improve skin elasticity.

Actipone Alpha Pulp is a key component in the development of face and body scrubs, offering gentle exfoliation with added moisturizing and antioxidant benefits.
Actipone Alpha Pulp is widely employed in the formulation of face mists, offering a quick and easy way to refresh and hydrate the skin throughout the day.
Actipone Alpha Pulp is used in the creation of bath products, providing a soothing and hydrating experience with added antioxidant protection.

Actipone Alpha Pulp is applied in the formulation of skincare products for sensitive skin, providing gentle hydration and protection without causing irritation.
Actipone Alpha Pulp is utilized in the development of moisturizing masks, offering deep hydration and antioxidant benefits for a radiant complexion.
Actipone Alpha Pulp is found in the formulation of skin-illuminating products, helping to enhance skin radiance and create a natural glow.



DESCRIPTION


Actipone Alpha Pulp is a high-quality natural extract derived from the pulp of apples, known for its potent antioxidant and skin-soothing properties.
Actipone Alpha Pulp is widely used in personal care formulations due to its ability to improve skin hydration, enhance radiance, and protect the skin from oxidative stress.

Actipone Alpha Pulp offers additional benefits such as anti-inflammatory and anti-aging effects, making it ideal for a wide range of skincare applications.
Actipone Alpha Pulp is often incorporated into formulations designed to brighten the skin, reduce the appearance of dark spots, and even out skin tone.
Actipone Alpha Pulp is recognized for its ability to enhance the overall texture and appearance of the skin, leaving it smooth, soft, and radiant.

Actipone Alpha Pulp is commonly used in natural and organic skincare formulations, where it provides a clean and effective alternative to synthetic ingredients.
Actipone Alpha Pulp is valued for its ability to support the skin's natural repair processes, making it a key ingredient in night creams and anti-aging treatments.
Actipone Alpha Pulp is a versatile ingredient that can be used in a variety of products, including moisturizers, serums, cleansers, and masks.

Actipone Alpha Pulp is an ideal choice for products targeting dry and sensitive skin, as it offers gentle yet effective hydration and protection.
Actipone Alpha Pulp is a key ingredient in formulations designed to combat the effects of environmental stressors, providing antioxidant protection against free radicals.
Actipone Alpha Pulp is known for its environmental friendliness, being derived from natural sources and offering a sustainable alternative to synthetic skincare ingredients.

Actipone Alpha Pulp enhances the overall effectiveness of personal care products by providing hydration, antioxidant protection, and skin conditioning in one ingredient.
Actipone Alpha Pulp is often chosen for formulations that require a balance between hydration and skin protection, ensuring a well-rounded approach to skincare.
Actipone Alpha Pulp is a reliable ingredient for creating products that offer a pleasant user experience, with a light, non-greasy feel and a natural, refreshing scent.

Actipone Alpha Pulp is an essential component in innovative skincare products that stand out in the market for their performance, safety, and natural origin.



PROPERTIES


Chemical Formula: N/A (Complex mixture of natural compounds)
Common Name: Actipone Alpha Pulp (Apple Pulp Extract)
Molecular Structure:
Appearance: Light yellow to amber liquid
Density: Approx. 1.0 g/cm³
Melting Point: N/A (liquid at room temperature)
Solubility: Soluble in water, soluble in alcohols and glycols
Flash Point: N/A (aqueous solution)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low



FIRST AID


Inhalation:
If Actipone Alpha Pulp is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of eye contact, flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
If Actipone Alpha Pulp is ingested, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of vapors.

Ventilation:
Ensure adequate ventilation when handling large amounts of Actipone Alpha Pulp to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Actipone Alpha Pulp.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Actipone Alpha Pulp in a cool, dry, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid inhalation of vapors and direct contact with skin and eyes.
Use explosion-proof equipment in areas where vapors may be present.


Storage:

Temperature:
Store Actipone Alpha Pulp at temperatures between 15-25°C as recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Actipone Alpha Pulp away from incompatible materials, including strong oxidizers.

Handling Equipment:
Use dedicated equipment for handling Actipone Alpha Pulp to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of cosmetic ingredients.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

ACTIVATED CARBON
ACETYLENE BLACK ACETYLENE CARBON BLACK ACTIVATED CARBON ACTIVATED CARBON DARCO G-60 ACTIVATED CHARCOAL ACTIVATED CHARCOAL NORIT ACTIVATED CHARCOAL NORIT(R) CALGON CPG CARBO ACTIVATUS CARBON CARBON 84 CARBON, ACTIVATED CARBON ATOMIC ABSORPTION STANDARD CARBON BLACK CARBON BLACK, ACETYLENE CARBON, DECOLORIZING CARBON, DECOLORIZING DARCO(R) CARBON, DECOLORIZING NORIT(R) A CARBON, DECOLORIZING NUCHAR(R) S-N CARBON FELT cas :440-44-0
ACTIVATED CARBON
DESCRIPTION:

Activated carbon is a form of carbon commonly used to filter contaminants from water and air, among many other uses.
Activated carbon is processed to have small, low-volume pores that increase the surface area available for adsorption (which is not the same as absorption) or chemical reactions.
Activated carbon is analogous to making popcorn from dried corn kernels: popcorn is light, fluffy, and its kernels have a high surface-area-to-volume ratio.



CAS NUMBER: 7440-44-0

EC NUMBER: 231-153-3

MOLECULAR FORMULA: C

MOLECULAR WEIGHT: 12.011 g/mol



DESCRIPTION:

Activated carbon is sometimes replaced by active.
Due to its high degree of microporosity, one gram of activated carbon has a surface area in excess of 3,000 m2 (32,000 sq ft) as determined by gas adsorption.
Activated carbon has a specific surface area in the range of 2.0–5.0 m2/g.
An activation level sufficient for useful application may be obtained solely from high surface area.

Further chemical treatment often enhances adsorption properties.
Activated carbon is usually derived from waste products such as coconut husks; waste from paper mills has been studied as a source.
These bulk sources are converted into charcoal before being 'activated'.
When derived from coal it is referred to as activated coal.

Activated carbon is a porous form of carbon which can be manufactured from a variety of carbonaceous raw materials.
The principal commercial products are made from coconut shell, coal, peat or wood.
The activation process involves treating the raw material with steam or chemicals, thereby developing a pore structure.
Activated carbon, known as activated charcoal, is characterised by a vast system of pores of molecular size within the carbon particles, resulting in the formation of a material with an extensive internal surface area.

Commercially available, activated carbons have surface areas from 400m2/g to more than 2000m2/g.
Activated carbon or activated charcoal is a porous element that traps compounds, primarily organic, present in a gas or liquid.
Activated carbon does this so effectively that it is the most widely used purifying agent by humans.
On the other hand, organic compounds are derived from the metabolism of living beings, and their basic structure consists of chains of carbon and hydrogen atoms.
These include all derivatives from the plant and animal world, including petroleum and the compounds obtained from it.

The property of a solid to adhere a flowing molecule to its walls is called “adsorption”.
The solid is called “adsorbent” and the molecule, “adsorbate”.
After filtration, which aims to retain solids in a fluid, there is no single purification process with more applications than activated carbon.
Activated carbon is an adsorption medium, its function is to adsorb organic molecules in its micro pores.
Activated carbon is activated by thermal or chemical processes to enhance its adsorption capacity.

Activated carbon has the ability to adsorb.
So, some people put charcoal in the refrigerator to get rid of bad odors.
The same happens when you put charcoal in a bucket of water.
Eliminates color, taste and odor.

Activated carbon involves making it porous to increase its absorbency.
One gram of Activated carbon has a surface area of about 50 square meters.
With activation, Activated carbon reaches 600 to 800 m2, i.e., a 12 to 16-fold increase.
Activated carbon is used to purify liquids and gases in a variety of applications, including municipal drinking water, food and beverage processing, odor removal, industrial pollution control.

Activated carbon is produced from carbonaceous source materials, such as coconuts, nutshells, coal, peat and wood.
The primary raw material used for activated carbon is any organic material with a high carbon content.
Adsorption is a process where a solid is used for removing a soluble substance from the water.
In this process active carbon is the solid.
Activated carbon is produced specifically so as to achieve a very big internal surface (between 500 - 1500 m2/g).
This big internal surface makes active carbon ideal for adsorption.

Active carbon comes in two variations: Powder Activated Carbon (PAC) and Granular Activated Carbon (GAC).
The Activated carbon version is mostly used in water treatment
Activated carbon is a porous solid able to coordinate to itself various types of molecules.
This interaction can be of merely physical nature (attraction between non-bonded atoms or Van der Waals forces) or physical- chemical origin and its strength can vary depending upon the type of molecule and the type of activated carbon.
Activated carbons are usually produced by steam activation process, during which carbon or starting materials containing carbon atoms are partially gasified by reacting with steam or other oxidizing gases.

Raw materials such as charcoal, bituminous coal, lignite, coconut charcoal, peat coke or hard wood are used.
In addition, chemical activation can also be used to activate raw materials containing cellulose.
Saw dust for example is treated with chemicals that have a dehydrating effect at high temperature.
Both processes result in porous carbon which consists in an extremely porous structure with highly developed internal surface that can range from 500 up to 1500 square meters per gram of carbon.

To cover a wide variety of applications, starting from raw activated carbons, manufactures more than 40 different activated carbon finished products which are differing in material origin, physical shape (granular, extrudated or powdered), surface area, pore volume distribution, mesh size and other physical properties, in addition to impregnated carbons for special applications.
Activated carbon, also known as activated charcoal, is a crude form of graphite, the substance used for pencil leads.
Activated carbon differs from graphite by having a random, imperfect structure which is highly porous over a broad range of pore sizes from visible cracks and crevices to molecular dimensions.

The graphite structure gives the carbon its very large surface area which allows the carbon to adsorb a wide range of compounds.
Activated carbon is a very useful adsorbent material with high porosity and high carbon content.
Activated carbon has a wide application range due to its pore structure, large surface area and high reactivity.
Activated carbons, which are economical absorbents for many industries, are used to remove odor and color, to purify and dechlorinate liquid and steam applications. Common uses are water treatment, food grade products, automotive applications, cosmetics, gas purification and industrial processes.

The main and common production materials of activated carbons are coconut shell, charcoal and wood.
Activated carbon (also called activated charcoal, activated coal or active carbon) is a very useful adsorbent.
Due to their high surface area, pore structure (micro, meso and macro), and high degree of surface reactivity, activated carbon can be used to purify, dechlorinate, deodorize and decolorize both liquid and vapor applications.
Moreover, activated carbons are economical adsorbents for many industries such as water purification, food grade products, cosmetology, automotive applications, industrial gas purification, petroleum and precious metal recovery mainly for gold.

The base materials for activated carbons are coconut shell, coal or wood.
Activated carbon has the strongest physical adsorption forces, or the highest volume of adsorbing porosity, of any material known to mankind.
Activated carbon can have a surface of greater than 1000m²/g.
This means 3g of activated carbon can have the surface area of a football field.
Activated carbon (activated charcoal) can made from many substances containing a high carbon content such as coal, coconut shells and wood.
The raw material has a very large influence on the characteristics and performance of the activated carbon.

Activated carbon is a highly porous substance that attracts and holds organic chemicals inside it.
The media is created by first burning a carbonaceous substance without oxygen which makes a carbon “char”.
Next, the “char” is treated chemically or physically to develop an interconnected series of “holes” or pores inside the carbon.
The great surface area of this internal pore network results in an extremely large surface area that can attract and hold organic chemicals.
Activated carbon attracts and holds organic chemicals from vapor and liquid streams cleaning them of unwanted chemicals.

Activated carbon does not have a great capacity for these chemicals, but is very cost effective for treating large volumes of air or water to remove dilute concentrations of contamination.
For a better perspective, when individuals ingest chemicals or are experiencing food poisoning, they are instructed to drink a small amount of activated carbon to soak up and remove the poisons.
Catalytic carbon is created by altering the surface structure of activated carbon.

Activated carbon is modified by gas processing at high temperatures to change the electronic structure and create the highest level of catalytic activity on carbon for reducing chloramine and H2S in water.
This added catalytic functionality is much greater than that found in traditional activated carbons.
Catalytic carbon is an economical solution to treat H2S levels as high as 20 to 30 ppm.
Activated carbon converts adsorbed H2S into sulfuric acid and sulfurous acid which are water soluble, so carbon systems can be regenerated with water washing to restore H2S capacity for less frequent physical change-outs.

Activated carbon, sometimes called activated charcoal, is a unique adsorbent prized for its extremely porous structure that allows it to effectively capture and hold materials.
Widely used throughout a number of industries to remove undesirable components from liquids or gases, activated carbon can be applied to an unending number of applications that require the removal of contaminants or undesirable materials, from water and air purification, to soil remediation, and even gold recovery.



USES:

Activated carbon is used in methane and hydrogen storage, air purification, capacitive deionization, supercapacitive swing adsorption, solvent recovery, decaffeination, gold purification, metal extraction, water purification, medicine, sewage treatment, air filters in respirators, filters in compressed air, teeth whitening, production of hydrogen chloride, edible electronics, and many other applications.


-Industrial:

One major industrial application involves use of activated carbon in metal finishing for purification of electroplating solutions.
For example, Activated carbon is the main purification technique for removing organic impurities from bright nickel plating solutions.
A variety of organic chemicals are added to plating solutions for improving their deposit qualities and for enhancing properties like brightness, smoothness, ductility, etc.
Due to passage of direct current and electrolytic reactions of anodic oxidation and cathodic reduction, organic additives generate unwanted breakdown products in solution.
Their excessive build up can adversely affect plating quality and physical properties of deposited metal.
Activated carbon treatment removes such impurities and restores plating performance to the desired level.


Medical:

Activated carbon is used to treat poisonings and overdoses following oral ingestion.
Tablets or capsules of activated carbon are used in many countries as an over-the-counter drug to treat diarrhea, indigestion, and flatulence.
However, Activated carbon shows no effect on intestinal gas and diarrhea, and is, ordinarily, medically ineffective if poisoning resulted from ingestion of corrosive agents, boric acid, petroleum products, and is particularly ineffective against poisonings of strong acids or bases, cyanide, iron, lithium, arsenic, methanol, ethanol or ethylene glycol.
Activated carbon will not prevent these chemicals from being absorbed into the human body.
Activated carbon is on the World Health Organization's List of Essential Medicines.


-Analytical chemistry:

Activated carbon, in 50% w/w combination with celite, is used as stationary phase in low-pressure chromatographic separation of carbohydrates using ethanol solutions (5–50%) as mobile phase in analytical or preparative protocols.

Activated carbon is useful for extracting the direct oral anticoagulants (DOACs) such as dabigatran, apixaban, rivaroxaban and edoxaban from blood plasma samples.
For this purpose it has been made into "minitablets", each containing 5 mg activated carbon for treating 1ml samples of DOAC.
Since this activated carbon has no effect on blood clotting factors, heparin or most other anticoagulants this allows a plasma sample to be analyzed for abnormalities otherwise affected by the DOACs.


-Environmental:

Activated carbon is usually used in water filtration systems.
In this illustration, the activated carbon is in the fourth level (counted from bottom).
Carbon adsorption has numerous applications in removing pollutants from air or water streams both in the field and in industrial processes such as:

-Spill cleanup
-Groundwater remediation
-Drinking water filtration
-Air purification
-Volatile organic compounds capture from painting, dry cleaning, gasoline dispensing operations, and other processes
-Volatile organic compounds recovery (solvent recovery systems, SRU) from flexible packaging, converting, coating, and other processes.

During early implementation of the 1974 Safe Drinking Water Act in the US, EPA officials developed a rule that proposed requiring drinking water treatment systems to use granular activated carbon.
Because of its high cost, the so-called GAC rule encountered strong opposition across the country from the water supply industry, including the largest water utilities in California.
Hence, the agency set aside the rule.
Activated carbon filtration is an effective water treatment method due to its multi-functional nature.
There are specific types of activated carbon filtration methods and equipment that are indicated – depending upon the contaminants involved.

Activated carbon is also used for the measurement of radon concentration in air.


-Agricultural:

Activated carbon is an allowed substance used by organic farmers in both livestock production and wine making.
In livestock production Activated carbon is used as a pesticide, animal feed additive, processing aid, nonagricultural ingredient and disinfectant.
In organic winemaking, activated carbon is allowed for use as a processing agent to adsorb brown color pigments from white grape concentrates.
Activated carbon is sometimes used as biochar.


-Distilled alcoholic beverage purification:

Activated carbon filters (AC filters) can be used to filter vodka and whiskey of organic impurities which can affect color, taste, and odor.
Passing an organically impure vodka through an activated carbon filter at the proper flow rate will result in vodka with an identical alcohol content and significantly increased organic purity, as judged by odor and taste.


-Fuel storage:

Research is being done testing various activated carbons' ability to store natural gas and hydrogen gas.
The porous material acts like a sponge for different types of gases.
The gas is attracted to the carbon material via Van der Waals forces.
Some carbons have been able to achieve bonding energies of 5–10 kJ per mol.
The gas may then be desorbed when subjected to higher temperatures and either combusted to do work or in the case of hydrogen gas extracted for use in a hydrogen fuel cell.

Gas storage in activated carbons is an appealing gas storage method because the gas can be stored in a low pressure, low mass, low volume environment that would be much more feasible than bulky on-board pressure tanks in vehicles.
The United States Department of Energy has specified certain goals to be achieved in the area of research and development of nano-porous carbon materials.
All of the goals are yet to be satisfied but numerous institutions, including the program, are continuing to conduct work in this field.


-Gas purification:

Filters with activated carbon are usually used in compressed air and gas purification to remove oil vapors, odor, and other hydrocarbons from the air.
The most common designs use a 1-stage or 2 stage filtration principle in which activated carbon is embedded inside the filter media.

Activated carbon filters are used to retain radioactive gases within the air vacuumed from a nuclear boiling water reactor turbine condenser.
Activated carbon beds adsorb these gases and retain them while they rapidly decay to non-radioactive solid species.
The solids are trapped in the charcoal particles, while the filtered air passes through.


-Chemical purification:

Activated carbon is commonly used on the laboratory scale to purify solutions of organic molecules containing unwanted colored organic impurities.

Filtration over activated carbon is used in large scale fine chemical and pharmaceutical processes for the same purpose.
Activated carbon is either mixed with the solution then filtered off or immobilized in a filter.


-Mercury scrubbing:

Activated carbon, often infused with sulfur or iodine, is widely used to trap mercury emissions from coal-fired power stations, medical incinerators, and from natural gas at the wellhead.
However, despite its effectiveness, activated carbon is expensive to use.
Since Activated carbon is often not recycled, the mercury-laden activated carbon presents a disposal dilemma.

If the activated carbon contains less than 260 ppm mercury, United States federal regulations allow it to be stabilized (for example, trapped in concrete) for landfilling.
However, waste containing greater than 260 ppm is considered to be in the high-mercury subcategory and is banned from landfilling.

Activated carbon is now accumulating in warehouses and in deep abandoned mines at an estimated rate of 100 tons per year.
The problem of disposal of mercury-laden activated carbon is not unique to the United States.
This mercury is largely recovered[citation needed] and the activated carbon is disposed of by complete burning, forming carbon dioxide (CO2).


-Food additive:

Activated carbon became a food trend in 2016, being used as an additive to impart a "slightly smoky" taste and a dark coloring to products including hotdogs, ice cream, pizza bases and bagels.
People taking medication, including birth control pills and antidepressants, are advised to avoid novelty foods or drinks that use activated charcoal coloring, as it can render the medication ineffective.


-Skin care:

The adsorbing aspects of activated charcoal have made it a popular additive in many skin care products.
Products such as Activated carbon Soaps and Activated Charcoal Face Masks and scrubs combine the use of the charcoal's adsorption ability along with the cleansing ability of soap.




USAGE AREAS:

-Drinking Water Treatment
-Waste Water Treatment
-Water Conditioning
-Chlorine Removal
-Air and Gas Purification
-Industrial Processes
-Pharmaceutical Industry
-Renewable Oils
-Automotive




APPLICATIONS:

-Water purification:

(carbon retains pesticides, greases, oils, detergents, disinfection by-products, toxins, color-producing compounds, compounds originating from the decomposition of algae and plants or from animal metabolism…).


-Deodorization and air purification:

For example: in cartridge respirators, air recirculation systems in public spaces, drain vents and water treatment plants, paint application booths, spaces that store or apply organic solvents.


-Treatment of people with acute intoxication:

Activated carbon is considered the “most universal antidote”, and is applied in emergency rooms and hospitals.



-Gold recovery:

Gold that cannot be separated from minerals by flotation processes is dissolved in sodium cyanide and adsorbed on activated carbon.



APPLICATION AREAS:

Different types of activated carbon are suited for various specialized applications.

-Granulated activated carbon
-Pelletized activated carbon
-Powdered activated carbon
-Impregnated activated carbon
-Catalytic activated carbon


-Activated carbon is used as a pigment in rubber tires, printing, shaping and drawing inks.
-Tire treads, belt covers and other wear-resistant rubber products; plastics as reinforcing agent, opacifier, electrical conductor, UV-light absorber; colorant for printing inks; carbon paper; typewriter ribbons; paint pigment; nucleating agent in air modifications; expanders on battery plates; It has many uses such as solar energy absorber.
-Used as car catalytic converters, vegetable oil/sugar/alcoholic beverage colorant, flue gas desulfurization agent, air purifier, dechlorinating agent (water treatment), adhesives and sealing chemicals.
-Activated carbon is used in copier/printer machine toner, corrosion inhibitors and anti-limescale agents, fuels and fuel additives, wire and cable insulation to provide an even distribution of electricity



BENEFITS:

-Removal of volatile organic compounds such as Benzene, TCE, and PCE.
-Hydrogen Sulfide (HS) and removal of waste gases
-Impregnated activated carbon used as a bacteria inhibitor in drinking water -filters
-Removal of taste and odor causing compounds such as MIB and geosmin
-Recovery of gold
-Removal of chlorine and chloramine


Designing a proper activated carbon filtration system with enough contact time, pressure drop, and vessel size is important.
Also, activated carbon’s physical and chemical characteristics play an important role in removing contaminants effectively.
Therefore, material testing is essential and ASTM test methods such as butane activity, surface area, density, and water content (moisture) can be carried out to find the best suitable material for your application.



FEATURES:

-Very high surface area characterized by a large proportion of micropores
-High hardness with low dust generation
-Excellent purity, with most products exhibiting no more than 3-5% ash content.
-Renewable and green raw material.



STRUCTURE OF ACTIVATED CARBON:

The structure of activated carbon has long been a subject of debate.
Activated carbon may have a structure related to that of the fullerenes, with pentagonal and heptagonal carbon rings.



PRODUCTION:

Activated carbon is carbon produced from carbonaceous source materials such as bamboo, coconut husk, willow peat, wood, coir, lignite, coal, and petroleum pitch.
Activated carbon can be produced (activated) by one of the following processes:


-Physical activation:

The source material is developed into activated carbon using hot gases.
Air is then introduced to burn out the gasses, creating a graded, screened and de-dusted form of activated carbon.
This is generally done by using one or more of the following processes:

Carbonization:

Material with carbon content is pyrolyzed at temperatures in the range 600–900 °C, usually in an inert atmosphere with gases such as argon or nitrogen


-Activation/oxidation:

Raw material or carbonized material is exposed to oxidizing atmospheres (oxygen or steam) at temperatures above 250 °C, usually in the temperature range of 600–1200 °C.
The activation is performed by heating the sample for 1 h in a muffle furnace at 450 °C in the presence of air.


-Chemical activation:

Activated carbon is impregnated with certain chemicals.
The chemical is typically an acid, strong base, or a salt (phosphoric acid 25%, potassium hydroxide 5%, sodium hydroxide 5%, potassium carbonate 5%, calcium chloride 25%, and zinc chloride 25%).
Activated carbon is then subjected to high temperatures (250–600 °C).
Activated carbon is believed that the temperature activates the carbon at this stage by forcing the material to open up and have more microscopic pores.
Chemical activation is preferred to physical activation owing to the lower temperatures, better quality consistency, and shorter time needed for activating the material.



CLASSIFICATION:

Activated carbons are complex products which are difficult to classify on the basis of their behaviour, surface characteristics and other fundamental criteria. However, some broad classification is made for general purposes based on their size, preparation methods, and industrial applications.


-Powdered activated carbon:

Normally, activated carbons (R 1) are made in particulate form as powders or fine granules less than 1.0 mm in size with an average diameter between 0.15 and 0.25 mm. Thus they present a large surface to volume ratio with a small diffusion distance.
Activated carbon (R 1) is defined as the activated carbon particles retained on a 50-mesh sieve (0.297 mm).
Activated carbon material is finer material.

Activated carbon is made up of crushed or ground carbon particles, 95–100% of which will pass through a designated mesh sieve.
The ASTM classifies particles passing through an 80-mesh sieve (0.177 mm) and smaller as PAC.
Activated carbon is not common to use PAC in a dedicated vessel, due to the high head loss that would occur.
Instead, Activated carbon is generally added directly to other process units, such as raw water intakes, rapid mix basins, clarifiers, and gravity filters.


-Granular activated carbon:

A micrograph of Activated carbon under scanning electron microscope
Activated carbon has a relatively larger particle size compared to powdered activated carbon and consequently, presents a smaller external surface. Diffusion of the adsorbate is thus an important factor.
Activated carbon is suitable for adsorption of gases and vapors, because gaseous substances diffuse rapidly.

Granulated carbons are used for air filtration and water treatment, as well as for general deodorization and separation of components in flow systems and in rapid mix basins.
Activated carbon can be obtained in either granular or extruded form.
Activated carbon is designated by sizes such as 8×20, 20×40, or 8×30 for liquid phase applications and 4×6, 4×8 or 4×10 for vapor phase applications.
The most popular aqueous-phase Activated carbon is the 12×40 and 8×30 sizes because they have a good balance of size, surface area, and head loss characteristics.


-Extruded activated carbon (EAC):

Extruded activated carbon (EAC) combines powdered activated carbon with a binder, which are fused together and extruded into a cylindrical shaped activated carbon block with diameters from 0.8 to 130 mm.
These are mainly used for gas phase applications because of their low pressure drop, high mechanical strength and low dust content.


-Bead activated carbon (BAC):

Bead activated carbon (BAC) is made from petroleum pitch and supplied in diameters from approximately 0.35 to 0.80 mm.
Similar to EAC, Activated carbon is also noted for its low pressure drop, high mechanical strength and low dust content, but with a smaller grain size.
Activated carbon's spherical shape makes it preferred for fluidized bed applications such as water filtration.


-Impregnated carbon:

Porous carbons containing several types of inorganic impregnate such as iodine and silver.
Cations such as aluminium, manganese, zinc, iron, lithium, and calcium have also been prepared for specific application in air pollution control especially in museums and galleries.
Due to its antimicrobial and antiseptic properties, silver loaded activated carbon is used as an adsorbent for purification of domestic water.

Drinking water can be obtained from natural water by treating the natural water with a mixture of activated carbon and aluminium hydroxide (Al(OH)3), a flocculating agent.
Impregnated carbons are also used for the adsorption of hydrogen sulfide (H2S) and thiols.
Adsorption rates for H2S as high as 50% by weight have been reported.


-Polymer coated carbon:

Woven activated carbon cloth
This is a process by which a porous carbon can be coated with a biocompatible polymer to give a smooth and permeable coat without blocking the pores.
The resulting carbon is useful for hemoperfusion.
Hemoperfusion is a treatment technique in which large volumes of the patient's blood are passed over an adsorbent substance in order to remove toxic substances from the blood.


-Woven carbon:

There is a technology of processing technical rayon fiber into activated carbon cloth for carbon filtering.
Adsorption capacity of activated cloth is greater than that of activated charcoal (BET theory) surface area: 500–1500 m2/g, pore volume: 0.3–0.8 cm3/g).
Thanks to the different forms of activated material, it can be used in a wide range of applications.



PROPERTIES:

A gram of activated carbon can have a surface area in excess of 500 m2 (5,400 sq ft), with 3,000 m2 (32,000 sq ft) being readily achievable.
Activated carbon has even higher surface areas, and are used in special applications.
Under an electron microscope, the high surface-area structures of activated carbon are revealed.
Individual particles are intensely convoluted and display various kinds of porosity; there may be many areas where flat surfaces of graphite-like material run parallel to each other, separated by only a few nanometers or so.

These micropores provide superb conditions for adsorption to occur, since adsorbing material can interact with many surfaces simultaneously.
Tests of adsorption behaviour are usually done with nitrogen gas at 77 K under high vacuum, but in everyday terms activated carbon is perfectly capable of producing the equivalent, by adsorption from its environment, liquid water from steam at 100 °C (212 °F) and a pressure of 1/10,000 of an atmosphere.
James Dewar, the scientist after whom the Dewar (vacuum flask) is named, spent much time studying activated carbon and published a paper regarding its adsorption capacity with regard to gases.

In this paper, he discovered that cooling the carbon to liquid nitrogen temperatures allowed it to adsorb significant quantities of numerous air gases, among others, that could then be recollected by simply allowing the carbon to warm again and that coconut based carbon was superior for the effect.
He uses oxygen as an example, wherein the activated carbon would typically adsorb the atmospheric concentration (21%) under standard conditions, but release over 80% oxygen if the carbon was first cooled to low temperatures.

Physically, activated carbon binds materials by van der Waals force or London dispersion force.
Activated carbon does not bind well to certain chemicals, including alcohols, diols, strong acids and bases, metals and most inorganics, such as lithium, sodium, iron, lead, arsenic, fluorine, and boric acid.
Activated carbon adsorbs iodine very well.
The iodine capacity, mg/g, (ASTM D28 Standard Method test) may be used as an indication of total surface area.

Carbon monoxide is not well adsorbed by activated carbon. This should be of particular concern to those using the material in filters for respirators, fume hoods or other gas control systems as the gas is undetectable to the human senses, toxic to metabolism and neurotoxic.
Substantial lists of the common industrial and agricultural gases adsorbed by activated carbon can be found online.
Activated carbon can be used as a substrate for the application of various chemicals to improve the adsorptive capacity for some inorganic (and problematic organic) compounds such as hydrogen sulfide (H2S), ammonia (NH3), formaldehyde (HCOH), mercury (Hg) and radioactive iodine-131(131I).
This property is known as chemisorption.


-Iodine number:

Activated carbons preferentially adsorb small molecules.
Iodine number is the most fundamental parameter used to characterize activated carbon performance.
Activated carbon is a measure of activity level (higher number indicates higher degree of activation[40]) often reported in mg/g (typical range 500–1200 mg/g).
Activated carbon is a measure of the micropore content of the activated carbon (0 to 20 Å, or up to 2 nm) by adsorption of iodine from solution.
Activated carbon is equivalent to surface area of carbon between 900 and 1100 m2/g.

Activated carbon is the standard measure for liquid-phase applications.
Iodine number is defined as the milligrams of iodine adsorbed by one gram of carbon when the iodine concentration in the residual filtrate is at a concentration of 0.02 normal (i.e. 0.02N).
Basically, iodine number is a measure of the iodine adsorbed in the pores and, as such, is an indication of the pore volume available in the activated carbon of interest.
Typically, water-treatment Activated carbons have iodine numbers ranging from 600 to 1100.

Frequently, this parameter is used to determine the degree of exhaustion of a carbon in use.
However, this practice should be viewed with caution, as chemical interactions with the adsorbate may affect the iodine uptake, giving false results.
Thus, the use of iodine number as a measure of the degree of exhaustion of a carbon bed can only be recommended if it has been shown to be free of chemical interactions with adsorbates and if an experimental correlation between iodine number and the degree of exhaustion has been determined for the particular application.



-Molasses:

Some carbons are more adept at adsorbing large molecules.
Molasses number or molasses efficiency is a measure of the mesopore content of the activated carbon (greater than 20 Å, or larger than 2 nm) by adsorption of molasses from solution.
A high molasses number indicates a high adsorption of big molecules (range 95–600).
Caramel dp (decolorizing performance) is similar to molasses number.
Molasses efficiency is reported as a percentage (range 40%–185%) and parallels molasses number (600 = 185%, 425 = 85%).
The European molasses number (range 525–110) is inversely related to the North American molasses number.


-Tannin:

Tannins are a mixture of large and medium size molecules.
Carbons with a combination of macropores and mesopores adsorb tannins.
The ability of a carbon to adsorb tannins is reported in parts per million concentration (range 200 ppm–362 ppm).
Molasses Number is a measure of the degree of decolorization of a standard molasses solution that has been diluted and standardized against standardized activated carbon.
Due to the size of color bodies, the molasses number represents the potential pore volume available for larger adsorbing species.

As all of the pore volume may not be available for adsorption in a particular waste water application, and as some of the adsorbate may enter smaller pores, it is not a good measure of the worth of a particular activated carbon for a specific application.
Frequently, this parameter is useful in evaluating a series of active carbons for their rates of adsorption.
Given two active carbons with similar pore volumes for adsorption, the one having the higher molasses number will usually have larger feeder pores resulting in more efficient transfer of adsorbate into the adsorption space.



-Methylene blue:

Some Activated carbons have a mesopore (20 Å to 50 Å, or 2 to 5 nm) structure which adsorbs medium size molecules, such as the dye methylene blue.
Methylene blue adsorption is reported in g/100g (range 11–28 g/100g).


-Dechlorination:

Activated carbons are evaluated based on the dechlorination half-life length, which measures the chlorine-removal efficiency of activated carbon.
The dechlorination half-value length is the depth of carbon required to reduce the chlorine concentration by 50%.
A lower half-value length indicates superior performance.


-Apparent density:

The solid or skeletal density of activated carbons will typically range between 2000 and 2100 kg/m3 (125–130 lbs./cubic foot).
However, a large part of an activated carbon sample will consist of air space between particles, and the actual or apparent density will therefore be lower, typically 400 to 500 kg/m3 (25–31 lbs./cubic foot).

Higher density provides greater volume activity and normally indicates better-quality activated carbon.
ASTM D 2854 -09 (2014) is used to determine the apparent density of activated carbon.



MODIFICATION OF PROPERTIES AND REACTIVITY:

Acid-base, oxidation-reduction and specific adsorption characteristics are strongly dependent on the composition of the surface functional groups.
The surface of conventional activated carbon is reactive, capable of oxidation by atmospheric oxygen and oxygen plasma steam, and also carbon dioxide and ozone.
Oxidation in the liquid phase is caused by a wide range of reagents (HNO3, H2O2, KMnO4).
Through the formation of a large number of basic and acidic groups on the surface of oxidized carbon to sorption and other properties can differ significantly from the unmodified forms.

Activated carbon can be nitrogenated by natural products or polymers or processing of carbon with nitrogenating reagents.
Activated carbon can interact with chlorine, bromine and fluorine.
Surface of activated carbon, like other carbon materials can be fluoralkylated by treatment with (per)fluoropolyether peroxide in a liquid phase, or with wide range of fluoroorganic substances by CVD-method.
Such materials combine high hydrophobicity and chemical stability with electrical and thermal conductivity and can be used as electrode material for super capacitors.

Sulfonic acid functional groups can be attached to activated carbon to give "starbons" which can be used to selectively catalyse the esterification of fatty acids. Formation of such activated carbons from halogenated precursors gives a more effective catalyst which is thought to be a result of remaining halogens improving stability.

Activated carbon is reported about synthesis of activated carbon with chemically grafted superacid sites –CF2SO3H.
Some of the chemical properties of activated carbon have been attributed to presence of the surface active carbon double bond.
The Polyani adsorption theory is a popular method for analyzing adsorption of various organic substances to their surface.



PHYSICAL FORM OF ACTIVATED CARBON:

Activated carbon can be produced in the form of powder, granules or cylindrical pellets.
Activated carbon is only applied in the purification of liquids; the carbon is dosed into a tank with agitation and then separated from the liquid by means of a filter suitable for retaining small particles (such as a filter press).

In the case of granular coal, it is produced in different particle size ranges, which are specified based on particle size or mesh number.
A 4 mesh, for example, is one that has four holes in each linear inch.
They are applied both in the purification of liquids and gases.

Pellets are used in gas treatment, since their cylindrical shape produces a lower pressure drop.
In the case that a granular coal or pellet is desired, if the raw material is not hard enough, Activated carbon can be reagglomerated with a binding agent that imparts hardness to prevent it from breaking when the fluid passes through.



ADSORPTION CAPACITY OF ACTIVATED CARBON:

The capacity of an activated carbon to retain a given substance is not only given by its surface area, but also by the proportion of pores whose size is adequate, i.e., a suitable little has a diameter of between one and five times the molecule to be adsorbed.
If this condition is met, the capacity can be between 20% and 50% of its own weight.



FORM OF ACTIVATED CARBON:

-Granular Activated Carbon (GAC):

irregular shaped particles with sizes ranging from 0.2 to 5 mm.
This type is used in both liquid and gas phase applications.


-Powder Activated Carbon (PAC):

pulverised carbon with a size predominantly less than 0.18mm (US Mesh 80).
These are mainly used in liquid phase applications and for flue gas treatment.


-Extruded Activated Carbon (EAC):

extruded and cylindrical shaped with diameters from 0.8 to 5 mm.
These are mainly used for gas phase applications because of their low pressure drop, high mechanical strength and low dust content.




HOW DOES IT WORK:

The atoms of carbon, comprising the large internal surface area of activated carbon, present attractive forces outward from the surface.
These forces, known as Van der Waals forces, attract the molecules of the surrounding gas or liquid.
The combination of these attractive forces and those of molecules in the surrounding medium result in the absorption of molecules at the surface of the activated carbon.
Some molecules have structures which make them more easily adsorbed than others and it is due to this that the separation of molecules is achieved.



PHYSICAL AND CHEMICAL PROPERTIES:

-Molecular Weight: 12.011 g/mol
-XLogP3-AA: 0.6
-Hydrogen Bond Donor Count: 0
-Hydrogen Bond Acceptor Count: 0
-Rotatable Bond Count: 0
-Exact Mass: 12 g/mol
-Monoisotopic Mass: 12 g/mol
-Topological Polar Surface Area: 0Ų
-Heavy Atom Count: 1
-Complexity: 0
-Isotope Atom Count: 0
-Defined Atom Stereocenter Count: 0
-Undefined Atom Stereocenter Count: 0
-Defined Bond Stereocenter Count: 0
-Undefined Bond Stereocenter Count: 0
-Covalently-Bonded Unit Count: 1
-Compound Is Canonicalized: Yes



SYNONYM:

05105_FLUKA
05110_FLUKA
05112_FLUKA
05113_FLUKA
05120_FLUKA
05123_FLUKA
101239-80-9
106907-70-4
109766-76-9
114680-00-1
115344-49-5
116788-82-0
12424-49-6
124760-06-1
12751-41-6
12768-98-8
12789-22-9
130960-03-1
131640-45-4
133136-50-2
1333-86-4
1343-03-9
137322-21-5
137906-62-8
138464-41-2
1399-57-1
147335-73-7
155660-93-8
156854-02-3
158271-80-8
159251-18-0
161551_SIAL
16291-96-6
16291-96-6 (Parent)
164973-65-3
179607-25-1
18002_RIEDEL
18002_SUPELCO
18006_RIEDEL
18008_RIEDEL
18008_SIAL
181719-82-4
182761-22-4
186708-92-9
186708-96-3
208519-32-8
208728-20-5
208728-21-6
214540-86-0
22874_FLUKA
22874_SIAL
242233_SIAL
242241_SIAL
242268_SIAL
242276_SIAL
26837-67-2
282863_ALDRICH
282863_SIAL
29204_FLUKA
29204_SIAL
29238_FLUKA
292591_SIAL
2P3VWU3H10
308068-56-6
326874-96-8
329428_SIAL
332461_ALDRICH
332461_SIAL
37196-29-5
37265-44-4
37265-48-8
37771_FLUKA
37771_SIAL
37996_FLUKA
37996_SIAL
390127_SIAL
39422-04-3
39434-34-9
39988_FLUKA
3B4-2186
429685-07-4
484164_ALDRICH
496537_ALDRICH
496545_ALDRICH
496553_ALDRICH
496561_ALDRICH
496588_ALDRICH
496596_ALDRICH
50814-81-8
51127_FLUKA
51127_SIAL
519308_ALDRICH
52623-24-2
53095-52-6
53663_FLUKA
53663_SIAL
53851-02-8
55353-42-9
55607-95-9
56257-79-5
56257-80-8
56274-59-0
566149-76-6
56729-25-0
56729-26-1
572497_ALDRICH
58517-29-6
58899_FLUKA
61512-59-2
633100_ALDRICH
636398_ALDRICH
63661-31-4
64365-11-3
64365-11-3 (activated)
64427-56-1
64900-31-8
65407-06-9
67167-41-3
675342_SIAL
681225-93-4
6C
72343_FLUKA
72343_SIAL
72536-89-1
72840-52-9
73560-38-0
7440-44-0
75026-75-4
76416-61-0
76632-92-3
7782-40-3
7782-42-5
798556-12-4
798556-14-6
79921-09-8
81180-26-9
82600-58-6
82696-74-0
82696-75-1
82701-02-8
82701-03-9
82701-04-0
82701-05-1
82701-06-2
82709-42-0
83138-28-7
83797-07-3
84739-05-9
857167-12-5
87934-03-0
89341_FLUKA
89341_SIAL
89440_ALDRICH
89440_FLUKA
90452-98-5
90597-58-3
93067_FLUKA
93067_SIAL
95681_FLUKA
95681_SIAL
96831_FLUKA
96831_SIAL
97708-44-6
97793-37-8
97876_FLUKA
97876_SIAL
AC1NUWBM
Acetylene black
Acticarbone
Actidose
Activated carbon
Activated charcoal
Activated Charcoal Norit
Activated Charcoal Norit(R)
Activated charcoal, iodinated
Adsorba
Adsorbit
Aerodag G
AG 1500
AG 3 (Adsorbent)
AG 5
AG 5 (Adsorbent)
AGN-PC-0LQUF1
AK (Adsorbent)
AKOS015914131
Amoco PX 21
Animal bone charcoal
Anthrasorb
Aqua nuchar
Aquadag
AR 3
Aroflow
Arogen
Arotone
Arovel
Arrow
ART 2
AS 1
AT 20
ATJ-S
ATJ-S graphite
Atlantic
AU 3
BAU
BG 6080
Black 140
Black Kosmos 33
Black lead
Black pearls
Bone charcoal
C
C.I. 77265
C.I. 77266
C.I. Pigment Black 10
C.I. Pigment Black 6
C.I. Pigment Black 7
C2194
C2764_SIAL
C2889_SIAL
C3014_SIAL
C3345_SIAL
C4386_SIAL
C5510_SIAL
C6289_SIAL
C9157_SIAL
Calcotone Black
Cancarb
Canesorb
Canlub
Carbo activatus
Carbo vegetabilis
Carbodis
Carbolac
Carbolac 1
Carbomet
Carbomix
Carbon
Carbon Activated
CARBON BLACK
Carbon Black BV and V
Carbon black, acetylene
Carbon black, channel
Carbon black, furnace
Carbon black, lamp
Carbon black, thermal
CARBON NANOTUBE
Carbon nanotube, single-walled
Carbon powder
Carbon, activate
Carbon, activated
Carbon, activated [UN1362] [Spontaneously combustible]
Carbon, amorphous
Carbon, colloidal
Carbon, Vitreous
Carbon-12
Carbone
carbonium
carbono
Carbopol Extra
Carbopol M
Carbopol Z 4
Carbopol Z Extra
Carbosieve
Carbosorbit R
Caswell No. 161
Cb 50
CCRIS 7235
CCRIS 8681
CCRIS 9467
Cecarbon
Ceylon Black Lead
CF 8
CF 8 (Carbon)
Channel black
Char, from refuse burner
Charbon
CHARCOAL
Charcoal bone
Charcoal activated
Charcoal activated Norit
Charcoal activated Norit(R)
Charcoal bone
Charcoal, activated
Charcoal, activated [USP]
Charcoal, except activated
Charcodote
CHEBI:27594
CI 77266
CI Pigment black 7
CK3
CLF II
CMB 200
CMB 50
Coke powder
Colgon BPL
Colgon PCB 12X30
Colgon PCB-D
Collocarb
Columbia carbon
Columbia LCK
Conductex
Conductex 900
Continex
Corax A
Corax P
CPB 5000
Croflex
Crolac
CUZ 3
CWN 2
D&C Black No. 2
D002244
D006108
Darco
DC 2
Degussa
Delussa Black FW
DIAMOND
Durex O
Eagle Germantown
EG 0
EINECS 215-609-9
EINECS 231-153-3
EINECS 231-953-2
EINECS 231-955-3
EINECS 264-846-4
Electrographite
ELF 78
Elftex
EPA Pesticide Chemical Code 016001
Essex
Excelsior
EXP-F
Explosion Acetylene Black
Explosion Black
Farbruss
Fecto
Filtrasorb
Filtrasorb 200
Filtrasorb 400
Flamruss
Formocarbine
Fortafil 5Y
FT-0621888
FT-0623469
Fullerene soot
Furnace black
Furnal
Furnex
Furnex N 765
Gas Black
Gas-furnace black
Gastex
GK 2
GK 3
GP 60
GP 60S
GP 63
Grafoil
Grafoil GTA
graphene
Graphite
Graphite (all forms except graphite fibers)
Graphite (natural), dust
Graphite (synthetic)
GRAPHITE, NATURAL
Graphite, synthetic
Graphitic acid
Graphnol N 3M
Grosafe
GS 2
GY 70
H 451
Hitco HMG 50
HSDB 2017
HSDB 5037
HSDB 7713
HSDB 953
Huber
Humenegro
Hydrodarco
I14-114468
I14-45191
I14-52609
IG 11
Impingement Black
Impingement carbons
Irgalite 1104
Jado
K 257
Ketjenblack EC
Kohlenstoff
Korobon
Kosmink
Kosmobil
Kosmolak
Kosmos
Kosmotherm
Kosmovar
Lamp black
Lampblack
LS-51900
LS-59580
MA 100 (Carbon)
Magecol
Medicinal carbon
Metanex
MG 1
Micronex
Miike 20
Mineral carbon
Modulex
Mogul
Mogul L
Molacco
Monarch 1300
Monarch 700
MPG 6
Neo Spectra Beads AG
Neo-spectra II
Neo-Spectra Mark II
Neotex
Niteron 55
Norit
NORIT A, U.S.P.
Nuchar
Oil-furnace Black
OU-B
P 33 (carbon black)
P1250
P68
Papyex
Peach black
Pelikan C 11/1431a
Pelletex
Permablak 663
PG 50
Philblack
Philblack N 550
Philblack N 765
Philblack O
Pigment black 6
Pigment black 7
Plumbago
Plumbago (graphite)
Printex
Printex 60
Pyro-Carb 406
Raven
Raven 30
Raven 420
Raven 500
Raven 8000
Rebonex
Regal
Regal 300
Regal 330
Regal 400R
Regal 600
Regal 99
Regal SRF
Regent
RL04457
Rocol X 7119
Royal spectra
RTR-024045
S 1
S 1 (Graphite)
Schungite
Sevacarb
Seval
Shawinigan Acetylene Black
Shell carbon
Shungite
Silver graphite
Single wall carbon nanotube
SKG
SKLN 1
SKT
SKT (adsorbent)
Special Black 1V & V
Special schwarz
Spheron
Spheron 6
Statex
Statex N 550
Sterling MT
Sterling N 765
Sterling NS
Sterling SO 1
Stove Black
SU 2000
Suchar 681
Super-carbovar
Super-spectra
Superba
Supersorbon IV
Supersorbon S 1
SWCNT
Swedish Black Lead
Swine fly ash
SWNT
Therma-atomic Black
Thermal Acetylene Black
Thermal black
Thermatomic
Thermax
Thermblack
Tinolite
TM 30
Toka Black 4500
Toka Black 5500
Toka Black 8500
TR-024045
U 02
Ucar 38
Ultracarbon
UN1362
UNII-2P3VWU3H10
UNII-4QQN74LH4O
UNII-4XYU5U00C4
Vitreous Carbon
VVP 66-95
W8209
Watercarb
Whetlerite
Witcarb 940
XE 340
XF 4175L
GRAPHITE POWDER
Carbon, decolorizing
grafito
Carbo activates
Carbon activado
Activated Coal
Coconut Charcoal
Medicinal charcoal
Synthetic Graphite
Carbon (ACN
Graphite (natural)
COVALZIN
1034343-98-0
CHARCOAL POWDER
CHC (CHRIS Code)
Graphite; (Mineral carbon)
Carbon; (Graphite, synthetic)
NATPURE BLACK LC9083
ACTIVATED CHARCOAL (II)
AST-120 (MART.)
Carbon; (Graphite, synthetic)
Graphite inhalable dust respirable
DTXSID801019028
ACTIVATED CHARCOAL (MART.)
Graphite, natural - Respirable dust
NA1362
ACTIVATED CHARCOAL (USP MONOGRAPH)
CHARCOAL, ACTIVATED (EP MONOGRAPH)
CHARCOAL, ACTIVATED (USP IMPURITY)
C2150
C2151
C2152
C2154
C2155
C2156
C2157
C2158
C3133
G0500
G0501
G0502


































ACTYLOL
Actylol is an environmentally benign solvent with effectiveness comparable to petroleum-based solvents.
Actylol is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.
Actylol, also known as lactic acid ethyl ester, is the organic compound with the formula CH3CH(OH)CO2CH2CH3.

CAS Number: 687-47-8
EC Number: 202-598-0
Molecular Formula: C5H10O3
Molecular Weight (g/mol): 118.13

Synonyms: ETHYL LACTATE, 97-64-3, Ethyl 2-hydroxypropanoate, Solactol, Actylol, Acytol, Lactic acid, ethyl ester, Ethyl 2-hydroxypropionate, Propanoic acid, 2-hydroxy-, ethyl ester, Lactate d'ethyle, 2-Hydroxypropanoic acid ethyl ester, Lactic Acid Ethyl Ester, Ethyl alpha-hydroxypropionate, FEMA No. 2440, Eusolvan, Ethyl lactate (natural), Ethylester kyseliny mlecne, Lactate d'ethyle [French], NSC 8850, HSDB 412, Ethylester kyseliny mlecne [Czech], 2-Hydroxypropionic Acid Ethyl Ester, EINECS 202-598-0, UN1192, Ethyl ester of lactic acid, BRN 1209448, UNII-F3P750VW8I, AI3-00395, F3P750VW8I, Ethyl .alpha.-hydroxypropionate, DTXSID6029127, CHEBI:78321, NSC-8850, 4-03-00-00643 (Beilstein Handbook Reference), ethyl d-lactate, Ethyl lactate,C5H10O3,97-64-3, EthylL-(-)-Lactate, ethyl-lactate, ethyl DL-lactate, DL-Ethyl Lactate, Milchsaureathylester, Nat. Ethyl Lactate, MFCD00065359, Ethyl racemic-lactate, lactic acid ethylester, (S)-(-)-2-Hydroxypropionic acid ethyl ester, PURASOLV ELS, VERTECBIO EL, Lactic acid-ethyl ester, ELT (CHRIS Code), Mono-Ethyl mono-lactate, ETHYL LACTATE [MI], (.+/-.)-Ethyl lactate, Ethyl 2-hydroxypropanoate #, ETHYL LACTATE [FCC], SCHEMBL22598, ETHYL LACTATE [FHFI], ETHYL LACTATE [HSDB], ETHYL LACTATE [INCI], ETHYL LACTATE [MART.], DTXCID509127, WLN: QVY1 & O2, ETHYL LACTATE [WHO-DD], CHEMBL3186323, (+-)-Ethyl 2-hydroxypropanoate, (+-)-Ethyl 2-hydroxypropionate, FEMA 2440, NSC8850, Tox21_200889, 2-hydroxy-propionic acid ethyl ester, NA1192, Ethyl lactate, >=98%, FCC, FG, AKOS009157222, LS-2733, UN 1192, (+/-)-LACTIC ACID ETHYL ESTER, CAS-97-64-3, NCGC00248866-01, NCGC00258443-01, (+/-)-ETHYL 2-HYDROXYPROPIONATE, AS-13500, SY030456, A9137, Ethyl lactate [UN1192] [Flammable liquid], Ethyl lactate, natural, >=98%, FCC, FG, Ethyl lactate, SAJ first grade, >=97.5%, FT-0626259, FT-0627926, FT-0651151, L0003, Ethyl lactate [UN1192] [Flammable liquid], EN300-115258, A845735, Q415418, J-521263, 2-[(4-benzylpiperazin-1-yl)methyl]isoindoline-1,3-dione, (±)-Ethyl 2 hydroxypropanoate, (±)-Ethyl 2-hydroxypropionate, (±)-Ethyl lactate, 2-Hydroxypropanoate d'éthyle [French] [ACD/IUPAC Name], 2-Hydroxypropanoic acid ethyl ester, 97-64-3 [RN], Ethyl 2-hydroxypropanoate [ACD/IUPAC Name], Ethyl ester of lactic acid, Ethyl lactate [ACD/Index Name] [Wiki], Ethyl α-hydroxypropionate, Ethyl α-hydroxypropionate, Ethyl-2-hydroxypropanoat [German] [ACD/IUPAC Name], MFCD00065359 [MDL number], OD5075000, Propanoic acid, 2-hydroxy-, ethyl ester [ACD/Index Name], QY1&VO2 [WLN], 2-hydroxypropionic acid ethyl ester, 4-03-00-00643 [Beilstein], Actylol, Acytol, DL-Ethyl Lactate, DL-Ethyllactate, DL-LACTIC ACID, ETHYL ESTER, Ethyl 2-hydroxy propanoate, Ethyl lactate,C5H10O3,97-64-3, Ethyl racemic-lactate, Ethylester kyseliny mlecne [Czech], ethyllactate, Ethyl-lactate, Eusolvan, Lactate d'ethyle [French], lactic acid ethyl ester, Lactic acid, ethyl ester, Lactic acid-ethyl ester, L-lactic acid ethyl ester, MFCD00077825 [MDL number], Milchs??ure??thylester, Propanoic acid, 2-hydroxy-, ethyl ester (9CI), Solactol, UN 1192

Actylol is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.
The odor of Actylol when dilute is mild, buttery, creamy, with hints of fruit and coconut.

Actylol is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 to < 100 tonnes per annum.
Actylol is used by consumers, by professional workers (widespread uses), in formulation or re-packing and at industrial sites.

Actylol, also known as lactic acid ethyl ester, is the organic compound with the formula CH3CH(OH)CO2CH2CH3.
Actylol is the ethyl ester of lactic acid.

A colorless liquid, Actylol is a chiral ester.
Being naturally derived, Actylol is readily available as a single enantiomer.

Actylol is commonly used as a solvent.
Actylol is considered biodegradable and can be used as a water-rinsible degreaser.

Actylol is an environmentally benign solvent with effectiveness comparable to petroleum-based solvents.
The worldwide solvent market is about 30 million pounds per year, where Actylol can have an important share.

Actylol is considered a chemical commodity and has attracted much attention in recent years, since Actylol is formed by the esterification reaction of ethanol and lactic acid, which can be generated from biomass raw materials through fermentation.
In this work, an overview regarding the main properties and applications of Actylol, as well as Actylol synthesis and production processes, with a particular emphasis on reactive/separation processes, is presented.

Actylol, lactic acid ethyl ester or 2-hydroxypropanoic acid ethyl ester is the chemical compound of lactic acid with ethanol in the form of an ester.
Depending on Actylol synthesis, Actylol is available as racemate or pure substance.

If Actylol is split back into Actylol starting materials ethanol and lactic acid (e.g. by a chemical reaction), Actylol can be decomposed in nature.
Esterases, naturally occurring enzymes, can also carry out the split back into the original materials.

Lactic acid ethyl ester is therefore considered a "green solvent", as Actylol does not leave any toxic decomposition products in the ecosystem.
This provides an advantage over chlorinated solvents or glycols or glycol ethers, which have a higher biological toxicity.

Also known as lactic acid ethyl ester, is a monobasic ester formed from lactic acid and ethanol, commonly used as a solvent hence the name “lactic acid ethyl ester”.
Actylol is considered biodegradable and can be used as a water-risible degreaser.
Actylol is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.

Actylol is produced from biological sources and can be either the Levo (S) form or Dextro (R) form, depending on the organism that is the source of the lactic acid.
The most biologically sourced Actylol is ethyl (−)-L-lactate (ethyl (S)-lactate).

Actylol is also produced industrially from petrochemical stocks, and this Actylol consists of the racemic mixture of Levo and Dextro forms.
In some jurisdictions, the natural product is exempt from many restrictions placed upon the use and disposal of solvents.
Because both enantiomers are found in nature, and because Actylol is easily biodegradable, Actylol is considered to be a “green solvent.”

Uses of Actylol:
Actylol is used as a solvent substitute for glycol ethers in photolithography in the semiconductor manufacturing industry.
Actylol is used in some nail polish removers.

Actylol is used as a solvent for resins, dyes, and coatings; has FDA approval for use as a food flavoring agent
Actylol is the active ingredient in many anti-acne preparations.

Uses at industrial sites:
Actylol is used in the following products: semiconductors, photo-chemicals, polymers, metal surface treatment products, non-metal-surface treatment products and washing & cleaning products.
Actylol is used in the following areas: formulation of mixtures and/or re-packaging.

Actylol is used for the manufacture of: electrical, electronic and optical equipment and machinery and vehicles.
Release to the environment of Actylol can occur from industrial use: in processing aids at industrial sites.

Industry Uses:
Processing aids, not otherwise listed
Solvent
Solvents (which become part of product formulation or mixture)

Consumer Uses:
Actylol is used in the following products: air care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, polishes and waxes, washing & cleaning products and cosmetics and personal care products.
Other release to the environment of Actylol is likely to occur from: indoor use as processing aid and outdoor use as processing aid.

Widespread uses by professional workers:
Actylol is used in the following products: polishes and waxes and washing & cleaning products.
Other release to the environment of Actylol is likely to occur from: indoor use as processing aid.

Industrial Processes with risk of exposure:
Semiconductor Manufacturing
Painting (Solvents)
Plastic Composites Manufacturing

Applications of Actylol:
Actylol is an excellent ingredient for formulating printing inks, coatings, resin cleaners, paint strippers, graffiti removers, ink cleaners, etc.
Actylol alone and is an ideal wipe solvent.

Actylol can be used in industrial coatings applications, primarily in coil, extrusion, wood furniture and fixtures, containers and closures, automotive finishes and machinery.
Actylol is 100% biodegradable, easy and inexpensive to recycle.

Due to Actylol low toxicity, Actylol is a popular choice across many different production scenarios.
Actylol is also used as a solvent with various types of polymers.
In the presence of water, acids and bases the chemical will hydrolyse into ethanol and lactic acid.

Because both enantiomers are found in nature, and because Actylol is easily biodegradable, Actylol is considered to be a "green solvent."
Actylol and Actylol aqueous solutions are used as sustainable media for organic synthesis.

Due to Actylol relatively low toxicity, Actylol is used commonly in pharmaceutical preparations, food additives, and fragrances.
Actylol is also used as solvent for nitrocellulose, cellulose acetate, and cellulose ethers.

Production of Actylol:
Actylol is produced from biological sources, and can be either the levo (S) form or dextro (R) form, depending on the organism that is the source of the lactic acid.
Most biologically sourced Actylol is ethyl (−)-L-lactate (ethyl (S)-lactate).
Actylol is also produced industrially from petrochemical stocks, and this Actylol consists of the racemic mixture of levo and dextro forms.

Methods of Manufacturing of Actylol:

Derivation: (a) By the esterification of lactic acid with ethanol; (b) by combining acetaldehyde with hydrogen cyanide to form acetaldehyde cyanohydrin, which is converted into Actylol by treating with ethanol and an inorganic acid.

d-Actylol is obtained from d-lactic acid by azeotropic distillation with ethyl alcohol or benzene in the presence of concentrated H2SO4.
The l-form is prepared in similar fashion starting from l-lactic acid.
The racemic product is prepared by boiling for 24 hours optically inactive lactic acid with ethyl alcohol in carbon tetrachloride, or with an excess of ethyl alcohol in the presence of chlorosulfonic acid, or in the presence of benzenesulfonic acid in benzene solution.

Handling and Storage of Actylol:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling Actylol must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Actylol without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Reactivity Profile of Actylol:

Actylol is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.

Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Fire Fighting of Actylol:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.
Do not use dry chemical extinguishers to control fires involving nitromethane (UN1261) or nitroethane (UN2842).

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto Actylol.
If Actylol can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.
For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn.

Accidental Release Measures of Actylol:

Isolation and Evacuation:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Cleanup Methods:
Use personal protective equipment.
Avoid breathing vapors, mist or gas.

Ensure adquate ventilation.
Remove all sources of ignition.

Evacuate personnel to safe areas.
Beware of vapors accumulating to form explosive concentrations.
Vopors can accumulate in low areas.

Disposal Methods of Actylol:
Recycle any unused portion of the material for Actylol approved use or return Actylol to the manufacturer or supplier.

Ultimate disposal of the chemical must consider:
Actylol's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations.
If Actylol is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Identifiers of Actylol:
CAS Number:
687-47-8 (L-isomer)
97-64-3 (racemate)
7699-00-5 (D-isomer)

ChemSpider: 13837423
ECHA InfoCard: 100.002.363
EC Number: 202-598-0
PubChem CID: 7344
RTECS number: OD5075000
UNII: F3P750VW8I
UN number: 1192
CompTox Dashboard (EPA): DTXSID6029127
InChI: InChI=1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
Key: LZCLXQDLBQLTDK-UHFFFAOYSA-N
InChI=1/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
Key: LZCLXQDLBQLTDK-UHFFFAOYAV
SMILES: CCOC(=O)C(C)O

Synonym(s): (S)-(-)-Actylol, L(-)-Lactic acid ethyl ester, (S)-(-)-2-Hydroxypropionic acid ethyl ester
Linear Formula: CH3CH(OH)COOC2H5
CAS Number: 687-47-8
Molecular Weight: 118.13
MDL number: MFCD00004518
EC Index Number: 211-694-1

CAS: 687-47-8
Molecular Formula: C5H10O3
Molecular Weight (g/mol): 118.13
MDL Number: MFCD00004518
InChI Key: LZCLXQDLBQLTDK-BYPYZUCNSA-N
PubChem CID: 92831
ChEBI: CHEBI:78322
IUPAC Name: ethyl (2S)-2-hydroxypropanoate
SMILES: CCOC(=O)C(C)O

Properties of Actylol:
Chemical formula: C5H10O3
Molar mass: 118.132 g·mol−1
Appearance: Colorless liquid
Density: 1.03 g/cm3
Melting point: −26 °C (−15 °F; 247 K)
Boiling point: 151 to 155 °C (304 to 311 °F; 424 to 428 K)
Solubility in water: Miscible
Solubility in ethanol
and most alcohols: Miscible
Chiral rotation ([α]D): −11.3°
Magnetic susceptibility (χ): -72.6·10−6 cm3/mol

vapor pressure: 1.6 hPa ( 20 °C)
Quality Level: 200
Assay: ≥99% (GC)
form: liquid
autoignition temp.: 400 °C
potency: >2000 mg/kg LD50, oral (Rat)
expl. lim.: 1.5-16.4 % (v/v)
pH: 4 (20 °C, 50 g/L in H2O)
kinematic viscosity: 2.7 cSt(25 °C)
bp: 154 °C/1013 hPa
mp: -25 °C
transition temp: flash point 53 °C
density: 1.03 g/cm3 at 20 °C
storage temp.: 2-30°C
InChI: 1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m0/s1
InChI key: LZCLXQDLBQLTDK-BYPYZUCNSA-N

Molecular Weight: 118.13 g/mol
XLogP3-AA: 0.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 3
Exact Mass:
118.062994177 g/mol
Monoisotopic Mass:
118.062994177 g/mol
Topological Polar Surface Area: 46.5Ų
Heavy Atom Count: 8
Complexity: 79.7
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Actylol:
Acidity: 0.1% max. (as lactic acid)
Melting Point: -26.0°C
Density: 1.0340g/mL
Boiling Point: 154.0°C
Flash Point: 46°C
Infrared Spectrum: Authentic
Assay Percent Range: 96% min. (GC)
Packaging: Glass bottle
Linear Formula: CH3CH(OH)CO2C2H5
Refractive Index: 1.4100 to 1.4160
Quantity: 250 mL
Beilstein: 03,264
Fieser: 17,135
Merck Index: 14,3817
Specific Gravity: 1.034
Specific Rotation Condition: − 10.00 (20.00°C neat)
Specific Rotation: − 10.00
Solubility Information: Solubility in water: soluble. Other solubilities: miscible with alcohols,ketones and esters
Formula Weight: 118.13
Percent Purity: 97%
Physical Form: Liquid
Chemical Name or Material: Ethyl L(-)-lactate

Structure of Actylol:
Dipole moment: 3.46 D

Related compounds of Actylol:
Lactic acid, MActylol

Related Products of Actylol:
Dimethyl Glutaconate (~10% Cis)
(E,E)-4,6-Dimethyl-2,4-heptadienoic Acid
3,6-Dimethyl-3-heptanol
1,1-Dimethoxybutane
(E)-6,6-Dimethyl-2-hept-1-en-4-yn-1-amine

Names of Actylol:

Regulatory process names:
2-Hydroxypropanoic acid ethyl ester
Actylol
Acytol
Ethyl 2-hydroxypropionate
Ethyl alpha-hydroxypropionate
ethyl DL-lactate
Ethyl lactate
ETHYL LACTATE
Ethyl lactate
ethyl lactate
Ethyl lactate (natural)
ethyl lactate ethyl DL-lactate
ethyl lactate; ethyl DL-lactate
Ethylester kyseliny mlecne
Lactate d'ethyle
Lactic acid, ethyl ester
Propanoic acid, 2-hydroxy-, ethyl ester
Solactol

Translated names:
DL-mleczan etylu (pl)
ester etylowy kwasu mlekowego (pl)
Ethyl DL-lactat (de)
ethyl-DL-laktát (cs)
ethyl-laktát (cs)
ethyl-laktát ethyl-DL-laktát (cs)
ethyllacta (da)
ethyllactaat (nl)
Ethyllactat (de)
Ethyllactat Ethyl DL-lactat (de)
etil DL-lactat (ro)
etil DL-laktat (sl)
etil lactat (ro)
etil lactat etil DL-lactat (ro)
etil laktat (sl)
etil laktat etil DL-laktat (sl)
etil-DL-laktat (hr)
etil-DL-laktatas (lt)
etil-DL-laktát (hu)
etil-DL-laktāts (lv)
etil-laktat (hr)
etil-laktát (hu)
etil-laktát etil-DL-laktát (hu)
etillaktatas (lt)
etillaktatas etil-DL-laktatas (lt)
etillaktāts (lv)
etyl-(RS)-laktát (sk)
etyl-laktát (sk)
etyllaktat (no)
etyllaktat (sv)
etyylilaktaatti (fi)
Etüül-DL-laktaat (et)
Etüüllaktaat (et)
lactate d'éthyle; DL-lactate d'éthyle; (fr)
lactato de etilo (es)
lactato de etilo (pt)
lattato di etile (it)
mleczan etylu (pl)
mleczan etylu DL-mleczan etylu ester etylowy kwasu mlekowego (pl)
γαλακτικό αιθυλο (el)
етил DL-лактат (bg)
етил лактат (bg)
етил лактат етил DL-лактат (bg)

IUPAC names:
2-ethoxypropanoic acid
ethyl (2R)-2-hydroxypropanoate
Ethyl (S)-2-hydroxypropanoate
ethyl 2-hydroxypropanoat
ETHYL 2-HYDROXYPROPANOATE
Ethyl 2-hydroxypropanoate
ethyl 2-hydroxypropanoate
Ethyl alpha hydroxypropionate
Ethyl DL Lactate
ethyl DL-lactate
ETHYL LACTATE
Ethyl Lactate
Ethyl lactate
ethyl lactate
ethyl lactate
ethyl lactate;
Ethyllactat
Ethyl 2-hydroxypropanoate

Other names:
Ethyl lactate
Lactic acid ethyl ester
2-Hydroxypropanoic acid ethyl ester
Actylol
Acytol

Other identifiers:
2676-33-7
607-129-00-7
97-64-3
ACUMER 1100
2-Acrylamido-2-methylpropanesulfonic acid-acrylic acid copolymer; Acrylic Acid-2-Acrylamido-2-MeJSylpropane Sulfonic Acid Copolymer (AA/AMPS); Acrylic Acid-2-Acrylic AMide-2-Methyl Propane Sulfonate-AMps CopolyMer; ACRYLIC ACID/ APSA COPOLYMER/HPA TERPOLYMER (AA/APSA/HPA); prop-2-enoic acid,2-(prop-2-enoylamino)butane-2-sulfonic acid; 2-acrylamido-2-methylpropanesulfonic acid-acrylic acid; 2-(1-oxoprop-2-enylamino)-2-butanesulfonic acid; 2-acrylamido-2-methylpropanesulfonic acid-acrylic acid copolymer; 2-Propenoic acid polymer with 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid CAS NO:40623-75-4
ACUMER 2000
ACUMER 2000 ACUMER 2000 Scale Inhibitor and Dispersant CHEMISTRY AND MODE OF ACTION ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: • Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. • Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readily fractured crystals that do not adhere well to surfaces and can be easily removed during cleaning operations. • Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomerating and depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groups adsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. STABILIZATION/DISPERSANCY PERFORMANCE ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. APPLICATIONS • Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, antiscalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programmes : - Phosphate based programmes. - Zinc based programmes. - Advanced all organic programmes in which ACUMER 2000 helps corrosion inhibitors onto metal surfaces. ACUMER 2000 has a synergic effect with the other additives in preventing scale as well as corrosion. BENEFITS OF ACUMER 2000 - Exhibits excellent thermal and chemical stability and can be used and stored over a broad range of temperatures and pH's. This stability enables the formulator to manufacture one-package treatments at high pH for maximum shelf life. - Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. - Keeps surfaces clean for maximum heat transfer and corrosion resistance. ACUMER 2000 Scale Inhibitor and Dispersant TEST METHOD ACUMER 2000 may be analyzed at use concentration with the Hach polyacrylate test kit. This kit employs a patented method developed by Rohm and Haas. SAFE HANDLING INFORMATION • Caution: - Contact may cause eye irritation and slight skin irritation. • First aid measures - Contact with skin: wash skin thoroughly with soap and water. Remove contaminated clothing and launder before rewearing. - Contact with eyes: flush eyes with plenty of water for at least 15 minutes and then call a physician. - If swallowed: if victim is conscious, dilute the liquid by giving the victim water to drink and then call a physician. If the victim is unconscious, call a physician immediately. Never give an unconscious person anything to drink. • Toxicity: - Acute oral (LD50 ) rats: >5g/kg. MATERIAL SAFETY DATA SHEETS Rohm and Haas company maintains Material Safety Data Sheet (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our products. Acumer 2000 Acumer 2000 is manufactured by DOW Chemical (Mid South Chemical is a “certified” repackager of Acumer™ products) Scale Inhibitor and Dispersant Copolymer stabilizer, scale inhibitor, and dispersant for cooling water treatment Description ACUMER 2000 is an excellent phosphate and zinc stabilizer and dispersant of inorganic particulates for anti-scale/anti-corrosion cooling water treatment formulations. Used in: Water treatment Cooling waters Reverse osmosis Industrial and potable Advantages Prevent the formation of deposits on heat transfer surfaces Prevent inorganic and sedimentation fouling Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates NSF-60 certification for RO potable water Inhibits precipitation of calcium, magnesium, and iron salts Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical Nature Carboxylate/Sulfonate copolymer Average Molecular Weight 4500 (Mw) Total Solids (%) 43 pH as is (at 25°C) 4 Bulk density (at 25°C) 1.21 Viscosity Brookfield (mPa.s/cps at 25°C) 400 Chemistry and Mode of Action ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readily fractured crystals that do not adhere well to surfaces and can be easily removed during cleaning operations. Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomerating and depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groups adsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. Stabilization/Dispersancy Performance ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. Applications Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, anti-scalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programs: -Phosphate based programs -Zinc based programs -Advanced All Organic programs in which ACUMER 2000 helps corrosion inhibitors, such as phosphonates, onto metal surfaces. Benefits of ACUMER 2000 Exhibits excellent thermal and chemical stability and can be used and stored over a broad range of temperatures and pH’s. This stability enables the formulator to manufacture one-package treatments at high pH for maximum shelf life. Exhibits exceptional stability in the presence of hypochlorite. Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. Keeps surfaces clean for maximum heat transfer and corrosion resistance. ACUMER 2000 Scale Inhibitor and Dispersant Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical nature Carboxylate/Sulfonate copolymer Average molecular weight 4500 (Mw) Total solids (%) 43 pH as is (at 25°C) 4 Bulk density (at 25°C) 1.21 Brookfield Viscosity (mPa.s/cps at 25°C) 400 Chemistry and Mode of Action ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readilyfractured crystals that do not adhere well to surfaces and can be easily removed during cleaningoperations. Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomeratingand depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groupsadsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them fromaggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. Stabilization/Dispersancy Performance ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. Applications Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, anti-scalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programs: Phosphate based programs. Zinc based programs. Advanced All Organic programs in which ACUMER 2000 helps corrosion inhibitors, such as phosphonates, onto metal surfaces. ACUMER 2000 has a synergic effect with the other additives in preventing scale as well as corrosion. Benefits of ACUMER 2000 Exhibits excellent thermal and chemical stability and can be used and stored over a broad range oftemperatures and pH's. This stability enables the formulator to manufacture one-package treatments athigh pH for maximum shelf life. Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. Keeps surfaces clean for maximum heat transfer and corrosion resistance. Test Method If a traceable polymer is required, OPTIDOSE 2000 offers identical performance to ACUMER 2000, with the ability to detect 0.5 ppm - 15 ppm without interferences. Material Safety Data Sheets Rohm and Haas Company maintains Material Safety Data Sheets (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas Company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our products. Acumer 2000 Copolymer stabilizer, dispersant, and scale inhibitor for cooling water treatment Description ACUMER 2000 is recommended for use in cooling water treatments. It is an excellent zinc and phosphate stabilizer and dispersant of inorganic particulates for anti-scale/anti-corrosion. Advantages of Acumer 2000 Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Prevents the formation of deposits on heat transfer surfaces Prevents inorganic and sedimentation fouling Inhibits precipitation of calcium, iron salts, and magnesium Used In Water treatment Cooling Towers Reverse osmosis Industrial and Potable ACUMER 2000 Scale Inhibitor and Dispersant CHEMISTRY AND MODE OF ACTION ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: • Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. • Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readily fractured crystals that do not adhere well to surfaces and can be easily removed during cleaning operations. • Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomerating and depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groups adsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. STABILIZATION/DISPERSANCY PERFORMANCE ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. APPLICATIONS • Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, antiscalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programmes : - Phosphate based programmes. - Zinc based programmes. - Advanced all organic programmes in which ACUMER 2000 helps corrosion inhibitors onto metal surfaces. ACUMER 2000 has a synergic effect with the other additives in preventing scale as well as corrosion. BENEFITS OF ACUMER 2000 - Exhibits excellent thermal and chemical stability and can be used and stored over a broad range of temperatures and pH's. This stability enables the formulator to manufacture one-package treatments at high pH for maximum shelf life. - Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. - Keeps surfaces clean for maximum heat transfer and corrosion resistance. ACUMER 2000 Scale Inhibitor and Dispersant TEST METHOD ACUMER 2000 may be analyzed at use concentration with the Hach polyacrylate test kit. This kit employs a patented method developed by Rohm and Haas. SAFE HANDLING INFORMATION • Caution: - Contact may cause eye irritation and slight skin irritation. • First aid measures - Contact with skin: wash skin thoroughly with soap and water. Remove contaminated clothing and launder before rewearing. - Contact with eyes: flush eyes with plenty of water for at least 15 minutes and then call a physician. - If swallowed: if victim is conscious, dilute the liquid by giving the victim water to drink and then call a physician. If the victim is unconscious, call a physician immediately. Never give an unconscious person anything to drink. • Toxicity: - Acute oral (LD50 ) rats: >5g/kg. MATERIAL SAFETY DATA SHEETS Rohm and Haas company maintains Material Safety Data Sheet (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our products. Acumer 2000 Acumer 2000 is manufactured by DOW Chemical (Mid South Chemical is a “certified” repackager of Acumer™ products) Scale Inhibitor and Dispersant Copolymer stabilizer, scale inhibitor, and dispersant for cooling water treatment Description ACUMER 2000 is an excellent phosphate and zinc stabilizer and dispersant of inorganic particulates for anti-scale/anti-corrosion cooling water treatment formulations. Used in: Water treatment Cooling waters Reverse osmosis Industrial and potable Advantages Prevent the formation of deposits on heat transfer surfaces Prevent inorganic and sedimentation fouling Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates NSF-60 certification for RO potable water Inhibits precipitation of calcium, magnesium, and iron salts Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical Nature Carboxylate/Sulfonate copolymer Average Molecular Weight 4500 (Mw) Total Solids (%) 43 pH as is (at 25°C) 4 Bulk density (at 25°C) 1.21 Viscosity Brookfield (mPa.s/cps at 25°C) 400 Chemistry and Mode of Action ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readily fractured crystals that do not adhere well to surfaces and can be easily removed during cleaning operations. Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomerating and depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groups adsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. Stabilization/Dispersancy Performance ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. Applications Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, anti-scalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programs: -Phosphate based programs -Zinc based programs -Advanced All Organic programs in which ACUMER 2000 helps corrosion inhibitors, such as phosphonates, onto metal surfaces. Benefits of ACUMER 2000 Exhibits excellent thermal and chemical stability and can be used and stored over a broad range of temperatures and pH’s. This stability enables the formulator to manufacture one-package treatments at high pH for maximum shelf life. Exhibits exceptional stability in the presence of hypochlorite. Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. Keeps surfaces clean for maximum heat transfer and corrosion resistance. ACUMER 2000 Scale Inhibitor and Dispersant Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical nature Carboxylate/Sulfonate copolymer Average molecular weight 4500 (Mw) Total solids (%) 43 pH as is (at 25°C) 4 Bulk density (at 25°C) 1.21 Brookfield Viscosity (mPa.s/cps at 25°C) 400 Chemistry and Mode of Action ACUMER 2000 copolymer combines two functional groups: strong acid (sulfonate) and weak acid (carboxylate) that provide optimal anti-scale/dispersant efficiency through the following different mechanisms: Solubility enhancement by threshold effect, which reduces precipitation of low solubility inorganic salts. Crystal modification, which deforms the growing inorganic salt crystal to give small, irregular, readilyfractured crystals that do not adhere well to surfaces and can be easily removed during cleaningoperations. Dispersing activity, which prevents precipitated crystals or other inorganic particules from agglomeratingand depositing on surfaces. The sulfonate groups increase the negative charge of the carboxylate groupsadsorbed onto particles and, by then, reinforce the repulsion between the particles, preventing them fromaggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. Stabilization/Dispersancy Performance ACUMER 2000 polymer is designed to provide superior stabilization of calcium phosphate. It also demonstrates excellent stabilization of zinc and calcium carbonate. In addition ACUMER 2000 is a strong dispersant in keeping the silt and commonly encountered inorganic particules suspended and in preventing their settling out onto heat transfer surfaces. Applications Stabilizer/Anti-scale deposition polymer for cooling water treatment Taking advantage of all its complementary properties and high performance as a stabilizer, anti-scalent and dispersant, ACUMER 2000 is particularly recommended for the majorities of the cooling water treatment programs: Phosphate based programs. Zinc based programs. Advanced All Organic programs in which ACUMER 2000 helps corrosion inhibitors, such as phosphonates, onto metal surfaces. ACUMER 2000 has a synergic effect with the other additives in preventing scale as well as corrosion. Benefits of ACUMER 2000 Exhibits excellent thermal and chemical stability and can be used and stored over a broad range oftemperatures and pH's. This stability enables the formulator to manufacture one-package treatments athigh pH for maximum shelf life. Provides superior iron tolerance when most of the commercially available polymers are desactivated in the presence of soluble iron in the system. Keeps surfaces clean for maximum heat transfer and corrosion resistance. Test Method If a traceable polymer is required, OPTIDOSE 2000 offers identical performance to ACUMER 2000, with the ability to detect 0.5 ppm - 15 ppm without interferences. Material Safety Data Sheets Rohm and Haas Company maintains Material Safety Data Sheets (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas Company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our products. Acumer 2000 Copolymer stabilizer, dispersant, and scale inhibitor for cooling water treatment Description ACUMER 2000 is recommended for use in cooling water treatments. It is an excellent zinc and phosphate stabilizer and dispersant of inorganic particulates for anti-scale/anti-corrosion. Advantages of Acumer 2000 Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Prevents the formation of deposits on heat transfer surfaces Prevents inorganic and sedimentation fouling Inhibits precipitation of calcium, iron salts, and magnesium Used In Water treatment Cooling Towers Reverse osmosis Industrial and Potable
ACUMER 3100
ACUMER 3100 ACUMER 3100 Acumer 3100 is manufactured by DOW Chemical (Mid South Chemical is a “certified” repackager of Acumer 3100 products) Iron Oxide Dispersant Terpolymer stabilizer and dispersant for water treatment Description ACUMER 3100 is a superior phosphate and zinc stabilizer in stressed cooling water systems and an excellent iron and sludge dispersant in boilers. Used in Water Treatment Cooling Water Boilers industrial reverse osmosis membrane anti-scalant Advantages Use avoids potential fouling situations and maintains maximum heat transfer Excellent boiler sludge dispersant Exceptional iron scale inhibitor and iron oxide dispersant Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical Nature Carboxylate/Sulfonate/Nonionic functional terpolymer Average Molecular Weight 4500 (Mw) Total Solids (%) 43.5 Active Solids (%) 39.5 pH as is (at 25°C) 2.5 Bulk density (at 25°C) 1.20 Viscosity Brookfield (mPa.s/cps at 25°C) 500 Neutralization 0.13g of NaOH (100%) per g of ACUMER 3100 Chemistry and Mode of Action ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate) and a nonionic that provide optimal dispersancy for most particules under a broad range of operating conditions: It’s carboxylate groups are most strongly attracted to particles surfaces, allowing strong dispersant absorption onto particles. It’s sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion preventing particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. It’s nonionic groups further enhance dispersancy by providing steric repulsion between particles. Dispersancy Performance It is an outstanding dispersant, far superior to other types of polymers especially for dispersing both dried and hydrated iron oxide, hydroxyapatite and calcium carbonate. It is also an excellent stabilizer for corrosion inhibitors such as phosphate, phosphonates and zinc. Applications Dispersant and stabilizer for use in all cooling water programs It excels in the harshest of cooling water conditions, such as extremely high or low Ryznar Indexes, high iron concentrations, high levels of zinc or phosphate added as treatment to the system. ACUMER 3100 is particularly recommended in advanced all-organic programs. The product will maintain excellent heat transfer by its superior dispersancy and, in addition, will help corrosion inhibition by controlling film formation of the organic corrosion inhibitors onto metal surfaces. Control of boiler sludge ACUMER 3100 terpolymer is the product of choice for boiler water treatment formulations as it provides unsurpassed control of boiler sludge. The polymer makes it possible to easily transport iron with calcium and phosphate containing sludges for removal during blowdown. Superior iron oxide dispersant, ACUMER 3100 is particularly recommended to control hydrated iron oxide in condensate return line. Thermal/Hydrolytic Stability ACUMER 3100 terpolymer is highly resistant to breakdown in aqueous solution under conditions of high temperature, pressure and pH. As a safety measure ACUMER 3100 is not recommended for boilers operating at pressure greater than 900 psig. ACUMER 3100 is very resistant to hydrolysis as well. The product does not lose its performance capability after storage at pH 13.5 for 6 months at ambient temperature. Acumer 3100 Iron Oxide Dispersant Terpolymer Stabilizer and Dispersant for Water Treatment Description Acumer 3100 is an excellent phosphate and zinc stabilizer in stressed cooling water systems and a superior iron and sludge dispersant in boilers. Advantages of Acumer 3100 Use avoids potential fouling situations and maintains maximum heat transfer Excellent boiler sludge dispersant Exceptional iron scale inhibitor and iron oxide dispersant Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Used In Water Treatment Cooling Water Boilers Typical Properties of Acumer 3100 ACUMER 3100 Terpolymer The Anti-Scale Deposition for “Stressed” Cooling Water Conditions ACUMER 3100 is a carboxylate/sulfonate/nonionic functional terpolymer. It is a superior dispersant and stabilizer for use in all cooling water programs. When other polymers fail under “stressed” conditions, ACUMER 3100 will maintain excellent heat transfer and low corrosion rates in the system. “Stressed” conditions are found in cooling waters containing high levels of calcium, iron, phosphate, or zinc either, naturally occurring in the feedwater or introduced via treatment. These circulating waters may have either a very low or a very high Ryznar Index since ACUMER 3100 performs well in waters with either a scaling or corrosion problem. It is an excellent anti-scalant agent and, also, a stabilizer for corrosion inhibitors such as phosphate and zinc. ACUMER 3100 will disperse particulate matter containing calcium, iron, and kaolin and prevent their adhesion to heat transfer surfaces. This terpolymer also prevents the precipitation of phosphonates, and zinc in circulating water with high amounts of calcium, iron, or alkalinity, to allow controlled film formation of these corrosion inhibitors at the metal surface and, thus, maintain low corrosion rates. PHYSICAL PROPERTIES The typical physical properties of ACUMER 3100 terpolymer are listed in Table 1. TABLE 1 TYPICAL PHYSICAL PROPERTIES CHEMISTRY AND MECHANISM OF ACTION ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate), and a nonionic that provide optimal dispersancy for most particulates under a broad range of operating conditions. Among the three functionalities, ACUMER 3100 carboxylate groups are most strongly attracted to particle surfaces, allowing strong dispersant adsorption onto particles. ACUMER 3100 sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion of similarly charged particles in the cooling water circuit. This repulsion prevents particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. ACUMER 3100 nonionic groups further enhance dispersancy by providing steric repulsion between particles. This multi-functional action contrasts sharply to other dispersants, such as polyacrylic acid or polymethacrylic acid, having only carboxylate functionality which can become strongly attached to certain particles, leaving little residual negative charge available to provide dispersancy. Other polymers, such as SSMA can provide better dispersancy than PAA or PMAA on some particle substrates, but do not have the nonionic group which allows ACUMER 3100 terpolymer to function on a broader range of potential foulants. DISPERSANCY PERFORMANCE ACUMER 3100 terpolymer outperforms polymaleic acid and competitive polymers under cooling water conditions. FIGURE 1. IRON OXIDE DISPERSANCY COOLING WATER CONDITIONS, pH = 7.5 –3– STABILIZED PHOSPHATE PROGRAM Stabilizers control the deposition of phosphate to allow the formation of a very thin protective film on metal surfaces but prevent excessive deposits that reduce heat transfer efficiency. The graphs in Figures 2-4 show that ACUMER 3100 is also the best stabilizer for orthophosphate in high levels of calcium and iron. FIGURE 2. COOLING WATER — STABILIZED PHOSPHATE PROGRAM ALL-ORGANIC cooling water treatments rely on high pH (8-9) and high alkalinity (>200 ppm, as CaCO3) to help passivate metal surfaces. Organic phosphonate is used to inhibit CaCO3 precipitation and forms a cathodic corrosion-inhibiting film of calcium phosphonate. A “yellow-metal” inhibitor, such as tolyltriazole, is frequently included to inhibit brass or copper corrosion. Polymers, such as ACUMER 3100, are used to disperse particulates, inhibit CaCO3 precipitation, and stabilize calcium phosphonate. ACUMER 3100 stands out as the superior polymer for this program. Figure 5 shows results from phosphonate stabilization tests which demonstrate the superiority of ACUMER 3100. FIGURE 5. COOLING WATER — ALL-ORGANIC PROGRAM FORMULATION STABILITY Formulated products containing inorganic polyphosphates or triazoles are packaged at a high pH to maintain stability of the concentrated formulation. Unlike some competitive polymers, ACUMER 3100 terpolymer exhibited no loss of performance after six months of storage at a pH of 13.5. TEST METHODS ACUMER 3100 terpolymer may be analyzed at use concentration with the Hach polyacrylate test kit. This kit employs a patented method developed by Rohm and Haas Company. The kit was jointly developed by Rohm and Haas Company and the Hach Company. MATERIAL SAFETY DATA SHEETS Rohm and Haas Company maintains Material Safety Data Sheets (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas Company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our product. Under the OSHA Hazard Communication Standard, workers must have access to and understand MSDS on all hazardous substances to which they are exposed. Thus, it is important that appropriate training and information be provided to all employees and that MSDS be available on any hazardous products in their workplace. Rohm and Haas Company sends MSDS on non-OSHA-hazardous as well as OSHA-hazardous products to both “bill-to” and “ship-to” locations of all our customers upon initial shipment (including samples) of all of our products. Updated MSDS are sent upon revision to all customers of record. In addition, MSDS are sent annually to all customers of record. PATENTS The use of ACUMER 3100 ACUMER 3100 Iron Oxide Dispersant Typical Properties These properties are typical but do not constitute specifications. Property Typical Values Appearance Clear solution to slightly hazy Chemical nature Carboxylate/Sulfonate/Nonionic functional terpolymer Average molecular weight 4500 (Mw) Total solids (%) 43.5 Active solids (%) 39.5 pH as is (at 25°C) 2.5 Bulk density (at 25°C) 1.20 Brookfield Viscosity (mPa.s/cps at 25°C) 200 Neutralization 0.13g of NaOH (100%) per g of ACUMER 3100 Chemistry and Mode of Action ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate) and a nonionic that provide optimal dispersancy for most particules under a broad range of operating conditions: • ACUMER 3100 carboxylate groups are most strongly attracted to particles surfaces, allowing strong dispersant absorption onto particles. • ACUMER 3100 sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion preventing particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. • ACUMER 3100 nonionic groups further enhance dispersancy by providing steric repulsion between particles. Dispersancy Performance ACUMER 3100 polymer is an exceptional dispersant, especially for dispersing both dried and hydrated iron oxide, hydroxyapatite and calcium carbonate. It is also an excellent stabilizer for corrosion inhibitors such as phosphate, phosphonates and zinc. Page 2 of 3 ®TM Trademark of The Dow Chemical Company (“Dow”) or an affiliated company of Dow 713-00005-0712-EN ACUMER 3100 07/2012, Rev. 0 Suggested Applications • Dispersant and stabilizer that can be used in cooling water programs ACUMER 3100 terpolymer excels in harsh cooling water conditions, such as extremely high or low Ryznar Indexes, high iron concentrations, high levels of zinc or phosphate added as treatment to the system. ACUMER 3100 is particularly recommended in advanced all-organic programs. The product can maintain excellent heat transfer by its exceptional dispersancy and, in addition, will help corrosion inhibition by controlling film formation of the organic corrosion inhibitors onto metal surfaces. • Control of boiler sludge ACUMER 3100 terpolymer is the product of choice for boiler water treatment formulations as it provides unsurpassed control of boiler sludge. The polymer makes it possible to easily transport iron with calcium and phosphate containing sludges for removal during blowdown. Superior iron oxide dispersant, ACUMER 3100 is particularly recommended to control hydrated iron oxide in condensate return line. Thermal/Hydrolytic Stability ACUMER 3100 terpolymer is highly resistant to breakdown in aqueous solution under conditions of high temperature, pressure and pH. As a safety measure ACUMER 3100 is not recommended for boilers operating at pressure greater than 900 psig. ACUMER 3100 is very resistant to hydrolysis as well. The product does not lose its performance capability after storage at pH 13.5 for 6 months at ambient temperature. Approval ACUMER 3100 is TUV approved for use in boilers under the reference: 06-KG-66. ACUMER 3100 Acumer 3100 is manufactured by DOW Chemical (Mid South Chemical is a “certified” repackager of Acumer 3100 products) Iron Oxide Dispersant Terpolymer stabilizer and dispersant for water treatment Description ACUMER 3100 is a superior phosphate and zinc stabilizer in stressed cooling water systems and an excellent iron and sludge dispersant in boilers. Used in Water Treatment Cooling Water Boilers industrial reverse osmosis membrane anti-scalant Advantages Use avoids potential fouling situations and maintains maximum heat transfer Excellent boiler sludge dispersant Exceptional iron scale inhibitor and iron oxide dispersant Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Typical Properties These properties are typical but do not constitute specifications. Appearance Clear solution to slightly hazy Chemical Nature Carboxylate/Sulfonate/Nonionic functional terpolymer Average Molecular Weight 4500 (Mw) Total Solids (%) 43.5 Active Solids (%) 39.5 pH as is (at 25°C) 2.5 Bulk density (at 25°C) 1.20 Viscosity Brookfield (mPa.s/cps at 25°C) 500 Neutralization 0.13g of NaOH (100%) per g of ACUMER 3100 Chemistry and Mode of Action ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate) and a nonionic that provide optimal dispersancy for most particules under a broad range of operating conditions: It’s carboxylate groups are most strongly attracted to particles surfaces, allowing strong dispersant absorption onto particles. It’s sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion preventing particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. It’s nonionic groups further enhance dispersancy by providing steric repulsion between particles. Dispersancy Performance It is an outstanding dispersant, far superior to other types of polymers especially for dispersing both dried and hydrated iron oxide, hydroxyapatite and calcium carbonate. It is also an excellent stabilizer for corrosion inhibitors such as phosphate, phosphonates and zinc. Applications Dispersant and stabilizer for use in all cooling water programs It excels in the harshest of cooling water conditions, such as extremely high or low Ryznar Indexes, high iron concentrations, high levels of zinc or phosphate added as treatment to the system. ACUMER 3100 is particularly recommended in advanced all-organic programs. The product will maintain excellent heat transfer by its superior dispersancy and, in addition, will help corrosion inhibition by controlling film formation of the organic corrosion inhibitors onto metal surfaces. Control of boiler sludge ACUMER 3100 terpolymer is the product of choice for boiler water treatment formulations as it provides unsurpassed control of boiler sludge. The polymer makes it possible to easily transport iron with calcium and phosphate containing sludges for removal during blowdown. Superior iron oxide dispersant, ACUMER 3100 is particularly recommended to control hydrated iron oxide in condensate return line. Thermal/Hydrolytic Stability ACUMER 3100 terpolymer is highly resistant to breakdown in aqueous solution under conditions of high temperature, pressure and pH. As a safety measure ACUMER 3100 is not recommended for boilers operating at pressure greater than 900 psig. ACUMER 3100 is very resistant to hydrolysis as well. The product does not lose its performance capability after storage at pH 13.5 for 6 months at ambient temperature. Acumer 3100 Iron Oxide Dispersant Terpolymer Stabilizer and Dispersant for Water Treatment Description Acumer 3100 is an excellent phosphate and zinc stabilizer in stressed cooling water systems and a superior iron and sludge dispersant in boilers. Advantages of Acumer 3100 Use avoids potential fouling situations and maintains maximum heat transfer Excellent boiler sludge dispersant Exceptional iron scale inhibitor and iron oxide dispersant Stabilizes corrosion inhibitors such as zinc, phosphates, and phosphonates Used In Water Treatment Cooling Water Boilers Typical Properties of Acumer 3100 ACUMER 3100 Terpolymer The Anti-Scale Deposition for “Stressed” Cooling Water Conditions ACUMER 3100 is a carboxylate/sulfonate/nonionic functional terpolymer. It is a superior dispersant and stabilizer for use in all cooling water programs. When other polymers fail under “stressed” conditions, ACUMER 3100 will maintain excellent heat transfer and low corrosion rates in the system. “Stressed” conditions are found in cooling waters containing high levels of calcium, iron, phosphate, or zinc either, naturally occurring in the feedwater or introduced via treatment. These circulating waters may have either a very low or a very high Ryznar Index since ACUMER 3100 performs well in waters with either a scaling or corrosion problem. It is an excellent anti-scalant agent and, also, a stabilizer for corrosion inhibitors such as phosphate and zinc. ACUMER 3100 will disperse particulate matter containing calcium, iron, and kaolin and prevent their adhesion to heat transfer surfaces. This terpolymer also prevents the precipitation of phosphonates, and zinc in circulating water with high amounts of calcium, iron, or alkalinity, to allow controlled film formation of these corrosion inhibitors at the metal surface and, thus, maintain low corrosion rates. PHYSICAL PROPERTIES The typical physical properties of ACUMER 3100 terpolymer are listed in Table 1. TABLE 1 TYPICAL PHYSICAL PROPERTIES CHEMISTRY AND MECHANISM OF ACTION ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate), and a nonionic that provide optimal dispersancy for most particulates under a broad range of operating conditions. Among the three functionalities, ACUMER 3100 carboxylate groups are most strongly attracted to particle surfaces, allowing strong dispersant adsorption onto particles. ACUMER 3100 sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion of similarly charged particles in the cooling water circuit. This repulsion prevents particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. ACUMER 3100 nonionic groups further enhance dispersancy by providing steric repulsion between particles. This multi-functional action contrasts sharply to other dispersants, such as polyacrylic acid or polymethacrylic acid, having only carboxylate functionality which can become strongly attached to certain particles, leaving little residual negative charge available to provide dispersancy. Other polymers, such as SSMA can provide better dispersancy than PAA or PMAA on some particle substrates, but do not have the nonionic group which allows ACUMER 3100 terpolymer to function on a broader range of potential foulants. DISPERSANCY PERFORMANCE ACUMER 3100 terpolymer outperforms polymaleic acid and competitive polymers under cooling water conditions. FIGURE 1. IRON OXIDE DISPERSANCY COOLING WATER CONDITIONS, pH = 7.5 –3– STABILIZED PHOSPHATE PROGRAM Stabilizers control the deposition of phosphate to allow the formation of a very thin protective film on metal surfaces but prevent excessive deposits that reduce heat transfer efficiency. The graphs in Figures 2-4 show that ACUMER 3100 is also the best stabilizer for orthophosphate in high levels of calcium and iron. FIGURE 2. COOLING WATER — STABILIZED PHOSPHATE PROGRAM ALL-ORGANIC cooling water treatments rely on high pH (8-9) and high alkalinity (>200 ppm, as CaCO3) to help passivate metal surfaces. Organic phosphonate is used to inhibit CaCO3 precipitation and forms a cathodic corrosion-inhibiting film of calcium phosphonate. A “yellow-metal” inhibitor, such as tolyltriazole, is frequently included to inhibit brass or copper corrosion. Polymers, such as ACUMER 3100, are used to disperse particulates, inhibit CaCO3 precipitation, and stabilize calcium phosphonate. ACUMER 3100 stands out as the superior polymer for this program. Figure 5 shows results from phosphonate stabilization tests which demonstrate the superiority of ACUMER 3100. FIGURE 5. COOLING WATER — ALL-ORGANIC PROGRAM FORMULATION STABILITY Formulated products containing inorganic polyphosphates or triazoles are packaged at a high pH to maintain stability of the concentrated formulation. Unlike some competitive polymers, ACUMER 3100 terpolymer exhibited no loss of performance after six months of storage at a pH of 13.5. TEST METHODS ACUMER 3100 terpolymer may be analyzed at use concentration with the Hach polyacrylate test kit. This kit employs a patented method developed by Rohm and Haas Company. The kit was jointly developed by Rohm and Haas Company and the Hach Company. MATERIAL SAFETY DATA SHEETS Rohm and Haas Company maintains Material Safety Data Sheets (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas Company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our product. Under the OSHA Hazard Communication Standard, workers must have access to and understand MSDS on all hazardous substances to which they are exposed. Thus, it is important that appropriate training and information be provided to all employees and that MSDS be available on any hazardous products in their workplace. Rohm and Haas Company sends MSDS on non-OSHA-hazardous as well as OSHA-hazardous products to both “bill-to” and “ship-to” locations of all our customers upon initial shipment (including samples) of all of our products. Updated MSDS are sent upon revision to all customers of record. In addition, MSDS are sent annually to all customers of record. PATENTS The use of ACUMER 3100 ACUMER 3100 Iron Oxide Dispersant Typical Properties These properties are typical but do not constitute specifications. Property Typical Values Appearance Clear solution to slightly hazy Chemical nature Carboxylate/Sulfonate/Nonionic functional terpolymer Average molecular weight 4500 (Mw) Total solids (%) 43.5 Active solids (%) 39.5 pH as is (at 25°C) 2.5 Bulk density (at 25°C) 1.20 Brookfield Viscosity (mPa.s/cps at 25°C) 200 Neutralization 0.13g of NaOH (100%) per g of ACUMER 3100 Chemistry and Mode of Action ACUMER 3100 terpolymer contains three functional groups: strong acid (sulfonate), weak acid (carboxylate) and a nonionic that provide optimal dispersancy for most particules under a broad range of operating conditions: • ACUMER 3100 carboxylate groups are most strongly attracted to particles surfaces, allowing strong dispersant absorption onto particles. • ACUMER 3100 sulfonate groups are only weakly attracted to the particle surface and retain some residual negative charge to provide repulsion preventing particles from aggregating into larger particles which can settle and deposit on tube surfaces and low flow areas. • ACUMER 3100 nonionic groups further enhance dispersancy by providing steric repulsion between particles. Dispersancy Performance ACUMER 3100 polymer is an exceptional dispersant, especially for dispersing both dried and hydrated iron oxide, hydroxyapatite and calcium carbonate. It is also an excellent stabilizer for corrosion inhibitors such as phosphate, phosphonates and zinc. Page 2 of 3 ®TM Trademark of The Dow Chemical Company (“Dow”) or an affiliated company of Dow 713-00005-0712-EN ACUMER 3100 07/2012, Rev. 0 Suggested Applications • Dispersant and stabilizer that can be used in cooling water programs ACUMER 3100 terpolymer excels in harsh cooling water conditions, such as extremely high or low Ryznar Indexes, high iron concentrations, high levels of zinc or phosphate added as treatment to the system. ACUMER 3100 is particularly recommended in advanced all-organic programs. The product can maintain excellent heat transfer by its exceptional dispersancy and, in addition, will help corrosion inhibition by controlling film formation of the organic corrosion inhibitors onto metal surfaces. • Control of boiler sludge ACUMER 3100 terpolymer is the product of choice for boiler water treatment formulations as it provides unsurpassed control of boiler sludge. The polymer makes it possible to easily transport iron with calcium and phosphate containing sludges for removal during blowdown. Superior iron oxide dispersant, ACUMER 3100 is particularly recommended to control hydrated iron oxide in condensate return line. Thermal/Hydrolytic Stability ACUMER 3100 terpolymer is highly resistant to breakdown in aqueous solution under conditions of high temperature, pressure and pH. As a safety measure ACUMER 3100 is not recommended for boilers operating at pressure greater than 900 psig. ACUMER 3100 is very resistant to hydrolysis as well. The product does not lose its performance capability after storage at pH 13.5 for 6 months at ambient temperature. Approval ACUMER 3100 is TUV approved for use in boilers under the reference: 06-KG-66.
ACUMER 5000
ACUMER 5000 (akumer 5000) (akümer 5000) An excellent scale inhibitor and dispersant for silica and magnesium silicate. # NSF-60 for potable water. The ACUMER 5000 (akumer 5000) (akümer 5000) mobile phone app helps estimate a suitable dosage in the maintenance formulation for cooling circuits. Uses of ACUMER 5000 (akumer 5000) (akümer 5000): Industrial water treatment Benefits of ACUMER 5000 (akumer 5000) (akümer 5000): Excellent scale inhibition for a variety of applications including cooling circuits, boilers and RO units. Properties of ACUMER 5000 (akumer 5000) (akümer 5000) These values are typical properties and are not intended for use in preparing specifications. Application of ACUMER 5000 (akumer 5000) (akümer 5000) Boilers, Cooling Water, Membranes of ACUMER 5000 (akumer 5000) (akümer 5000) Phosphorus Free Yes Potable Approval of ACUMER 5000 (akumer 5000) (akümer 5000) Yes Scale Control / Inhibition of ACUMER 5000 (akumer 5000) (akümer 5000) Calcium Carbonate, Calcium Phosphate / Phosphonate, Iron Oxide Dispersion, Silica / Silicate ACUMER 5000 (akumer 5000) (akümer 5000) Multipolymer for Silica and Magnesium Silicate Scale Control Cooling water reuse is frequently limited by a ceiling on the amount of tolerable silica in the recirculation water. Normally, if silica levels exceed about 180 ppm SiO2, severe scaling can occur on heat transfer surfaces. Moreover, the scale that forms is frequently difficult or impossible to remove by conventional means. ACUMER 5000 (akumer 5000) (akümer 5000) silica control polymer has now raised that ceiling to at least 300 ppm SiO2, proven by exacting pilot studies and field trials, allowing for greater water reuse than ever before. ACUMER 5000 (akumer 5000) (akümer 5000) polymer prevents silica-based scale formation by dispersing colloidal silica and by preventing magnesium silicate scale formation at the heat transfer surfaces. The unique features of ACUMER 5000 (akumer 5000) (akümer 5000) polymer in the treatment of silica limited cooling water are presented below PHYSICAL PROPERTIES of ACUMER 5000 (akumer 5000) (akümer 5000) The typical physical properties of ACUMER 5000 (akumer 5000) (akümer 5000) polymer are listed in Table 1. TABLE 1 TYPICAL PHYSICAL PROPERTIES (these do not constitute specifications) of ACUMER 5000 (akumer 5000) (akümer 5000) Molecular Weight of ACUMER 5000 (akumer 5000) (akümer 5000) 5000 Total Solids, % 44.5 to 45.5 Active Solids, % 42 pH 2.1 to 2.6 Brookfield Viscosity of ACUMER 5000 (akumer 5000) (akümer 5000), cp 700 max. Specific Gravity of ACUMER 5000 (akumer 5000) (akümer 5000) 1.2 Bulk Density, lb/gal (g/cc) 10 (1.19) Lb (Kg) of 100% NaOH to neutralize 1 lb (kg) of polymer 0.131 FORMATION OF SILICA-BASED SCALE of ACUMER 5000 (akumer 5000) (akümer 5000) Silica forms particles with different structures depending upon the pH, presence of other ions and process by which the particles are formed. The three main forms of silica encountered in cooling water are: • Molybdate-reactive silica: frequently referred to as dissolved silica. • Colloidal silica: polymerized silica particles of 0.1 micron or less. • Silicate scale: primarily magnesium silicate, but may also be iron or calcium silicate. Colloidal silica, which forms when the solubility level of silica is exceeded, is difficult to measure under field conditions, and a total silica mass balance cannot be achieved with a simple field test. The most effective method of determining total silica is described in “Standard Methods for the Examination of Water and Wastewater”, 17th edition (Method 4500-SiC). A simpler method that converts other forms of silica to molybdate-reactive silica is described in Rohm and Haas Technical Bulletin FC-267, “ACUMER TST sm, Total Silica Test for High-Silica Waters”. As the colloidal silica passes into the Nernst diffusion layer at the heat transfer surface, it dissolves and acquires a negative (anionic) charge. Polyvalent cations, especially magnesium, tend to react with these anionic colloidal particles effectively “gluing” them together and ultimately forming a hard, glassy magnesium silicate scale. Figure 1 shows how colloidal silica can dissolve to form silicate in the high temperature/high pH environment near a corroding cathodic surface where dissolved oxygen is reduced to hydroxide ions. These freshly formed silicate anions, added to the dissolved silica already present, can then form magnesium silicate scale (MgSiO3). In addition, colloidal silica alone can coprecipitate with magnesium hydroxide to form a scale of magnesium silicate having non-stoichiometric ratios of magnesium to silicate. Mechanism for Controlling Silica ACUMER 5000 (akumer 5000) (akümer 5000) The remarkable properties of ACUMER 5000 (akumer 5000) (akümer 5000) polymer derive in large part from its three distinctive functionalities. The weak acid (carboxylate) group provides a means of attaching the polymer to metal ions in solution and to the surfaces of particles or crystals. This enables the polymer to act as a dispersant to prevent agglomeration and deposit formation as well as stabilizing contaminants. The strong acid (sulfonate) contributes to this process by increasing the solubility and charge density of the polymer which enhances electrostatic repulsion of particles. What sets ACUMER 5000 (akumer 5000) (akümer 5000) polymer apart, however, is a unique third set of functionalities, based on balanced hydrophilicity and lipophilicity (hydrophobicity)1 . ACUMER 5000 (akumer 5000) (akümer 5000) Where the other functionalities operate primarily through charge-transfer, this so-called HLB functionality promotes physical adsorption on the surfaces of contaminant particles especially at higher temperatures. By promoting adsorption, this third type of functionality also contributes to the strength of the energy barrier (or the net repulsive force) created by the polymer around the silica particle. ACUMER 5000 (akumer 5000) (akümer 5000) polymer adsorbed on the colloid surfaces provides an energy barrier that prevents precipitation and agglomeration. Moreover, even if the silica particles precipitate, they are spaced too far apart for magnesium or redissolved silicate anions to bind them together. As a result, the scale formed by these particles will be powdery and, thus, easier to remove. For additional information on these mechanisms please request the following reprints: “Control of Iron and Silica with Polymeric Dispersants”, “Recent Experience in Controlling Silica and Magnesium Silicate Deposits with Polymeric Dispersants” 1The idea of enhancing adsorption by balancing hydrophilic and lipophilic moieties is borrowed from surfactant chemists who use the term HLB (hydrophile/ lipophile balance) to describe surfactant solubility and adsorption characteristics. ACUMER 5000 (akumer 5000) (akümer 5000) polymer does not actually have surfacant-like properties, but it behaves in an analogous way. MAGNESIUM SILICATE SCALE ACUMER 5000 (akumer 5000) (akümer 5000) PREVENTION WITH ACUMER 5000 (akumer 5000) (akümer 5000) POLYMER ACUMER 5000 (akumer 5000) (akümer 5000) Polymer Action in Recirculating Water Photomicrographs using cross-polarized lenses can be used to study crystal structures. Figure 3 shows the dispersed silica using ACUMER 5000 (akumer 5000) (akümer 5000) polymer in the recirculating water versus agglomerated silica particles in Figure 2 without polymer. ACUMER 5000 (akumer 5000) (akümer 5000) Polymer Action at Heat Transfer Surface ACUMER 5000 (akumer 5000) (akümer 5000) silica control polymer also prevents formation of magnesium silicate under the conditions found near a heat transfer surface, as shown in Figures 4 and 5. PERFORMANCE OF ACUMER 5000 (akumer 5000) (akümer 5000) POLYMER Accelerated Pilot Cooling Tower Tests of ACUMER 5000 (akumer 5000) (akümer 5000) A series of 3-day pilot cooling tower (PCT) tests were run to compare the dispersing efficiency of ACUMER 5000 (akumer 5000) (akümer 5000) polymer with that of conventional products. The water chemistry and operating parameters of the PCT in these studies are shown in Tables 2 and 3. The treatment formulation used to evaluate polymer efficacy consisted of 2 ppm tolyltriazole (TTA), 10 ppm active polymer, and a 1/1 blend of 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTC) and 1-hydroxyethylidene-1,1-diphosphonic acid (HEDP) to give 5 ppm total active phosphonate. At start-up, the formulation was fed into the system at three times the normal strength to compensate for the high concentrations of silica, calcium and magnesium.In these accelerated tests, water passed over a series of four heat transfer rods in succession. Scale formed on all four rods, with each developing more scale than its immediate predecessor. This progressive deposition was caused by the water becoming hotter as it passed over the rods in succession. As the water temperature rose, the tendency for deposits to form increased. In repeat tests, the amount of scale fluctuated dramatically when the polymer was an ineffective scale inhibitor. ACUMER 5000 (akumer 5000) (akümer 5000) polymer shows only a light dusting of scale (Figure 6), considerably better than the other polymers tested (Figures 7 and 8). Within the limits of experimental error, the scale compositions obtained with all tests were approximately the same, >80% magnesium silicate (Table 5). Long-Term Pilot Cooling Tests of ACUMER 5000 (akumer 5000) (akümer 5000) ACUMER 5000 (akumer 5000) (akümer 5000) polymer was compared to the two polymers from the previous trials in longer tests; 1) to determine whether concentrating the water too rapidly gave an artificial negative effect, 2) to analyze scale that might form in the cooler parts of the PCT, and 3) to measure the impact of the polymer on corrosion. These products were evaluated in the same water under the same conditions employed in the accelerated PCT tests (Tables 2 and 3); only the cycling rate and start-up conditions were different. In the long-term trials, the water was started at 3 cycles of concentration (COC), using 2.5 times the normal treatment level, and then maintained at 5.5 COC (275 ppm SiO2) for four days to allow any silicate salts or silica to form, grow and precipitate. The water was then concentrated further to between 7.2 and 7.5 cycles of concentration over the next nine days of the test to reach a theoretical concentration of between 360 and 375 ppm SiO2 (50 ppm X 7.5). This quantity is approximately double the recommended maximum for cooling water. The results of these tests are given in Table 6. The results indicate that under the test conditions, ACUMER 5000 (akumer 5000) (akümer 5000) silica control polymer yields 10 times less silica-based scale than conventional polymaleic acid chemistry and 5 to 6 times less scale than the commercial silica control polymer. Moreover, the corrosion rate with ACUMER 5000 (akumer 5000) (akümer 5000) polymer is much lower than with the two other polymers. The large difference in corrosion rates may be due to underdeposit corrosion occurring with the less effective polymers. FIELD PERFORMANCE of ACUMER 5000 (akumer 5000) (akümer 5000) The benefits of ACUMER 5000 (akumer 5000) (akümer 5000) polymer have been substantiated by its performance in four field situations. In each instance, operators of the different facilities faced the problem of processing water that contained high silica levels and all overcame their difficulties by using ACUMER 5000 (akumer 5000) (akümer 5000) polymer in their cooling water treatment program. Chiller System Achieves 80% Increase in COC Plus On-Line Cleaning System Two 250-ton cooling water units with a recirculation rate of 580 gpm were used Description: to cool a high school. The units were treated with a chromate program until 1990. In March of 1990, the chromate treatment was replaced with molybdate/ zinc/phosphonate to comply with regulations against chromate. Deposits were controlled using 7-8 ppm active ACUMER 2000 copolymer. The pH of the system was maintained at 7.5 - 8.5. Problem: Total hardness of the makeup water was typically about 140 ppm, with a Ca/Mg ratio of about 1/1. The makeup water typically had about 45 ppm SiO2, and the system could only achieve about 2.5 cycles of concentration using the molybdate/phosphonate/zinc copolymer treatment. The condenser was opened in 1991 and found to have light scale containing about 25% silica with most of the balance being iron oxide. Solution: In one of the chiller systems, the copolymer was replaced with an equal concentration of ACUMER 5000 (akumer 5000) (akümer 5000) polymer and blowdown was reduced; all other variables remained the same. The other chiller system was maintained with the program containing ACUMER 2000 copolymer. Results: The system treated with ACUMER 5000 (akumer 5000) (akümer 5000) polymer achieved more than 4.5 cycles of concentration with no silica drop-out. Early in this trial, the chemical feed was stopped accidentally; a subsequent drop in recirculating water SiO2 levels suggests that some scaling probably occurred. When the chemical feed was re-established, SiO2 levels temporarily increased to higher than expected levels, which leads to the conclusion that the ACUMER 5000 (akumer 5000) (akümer 5000) polymer had removed some of the scale. This also suggests that the dispersing action of the polymer, even when underfed, resulted in the formation of a powdery scale rather than the expected glassy magnesium silicate. The powdery nature of the scale would explain its apparent on-line removal. Data showed that over 200 ppm SiO2 had been attained in the recirculating water. Winery Increases Silica in Cooling Water Past Vintage Levels of 150 ppm SiO2 System A northern California vineyard operates two 560-ton evaporative condensers using Descripion: makeup water1 with high silica levels of 92 ppm SiO2. The cooling water system has a capacity of 18 gallons per minute with water temperatures ranging between 75°F (24°C) and 85°F (29°C). Problem: Initially, a stabilized phosphate program containing HEDP, phosphoric acid, tolyltriazole and an acrylate-type polymer was used. Scale formed on the evaporative condensers when silica levels exceeded 150 ppm SiO2 in the recirculating water. This deposit was found to contain high levels of silicon and magnesium. Results: Our customer replaced the existing polymer in his formulation with ACUMER 5000 (akumer 5000) (akümer 5000) polymer. This formulation was dosed into the system to maintain 13 ppm residual orthophosphate and 10-15 ppm active ACUMER 5000 (akumer 5000) (akümer 5000) polymer in the recirculating water. The recirculating water contains 400 ppm M-Alkalinity and had a pH between 8.5 and 8.7. The customer was able to increase cooling water cycles from 1.6 to 3 COC allowing up to 276 ppm SiO2 in the system. Thorough visual inspections, after 2 and 5 months, condenser tubes were free of scale. By switching to ACUMER 5000 (akumer 5000) (akümer 5000) polymer, this customer was able to cut his chemical usage by almost half and save 4 million gallons of water per year. 1 Make-up water analysis: pH 7.8, 138 ppm T-Alkalinity, 92 ppm SiO2, 35 ppm Ca as CaCO3, 11 ppm Mg, 7.4 ppm SO4, 18 ppm Cl, <0.1 ppm Fe, <0.3 ppm Mn, 270 ppm TDS. Cooling System Doubles COC in San Joaquin Valley, California System Two evaporative condenser towers rated at 500 tons were used to cool a large computer Description: computer facility. One tower was always kept as a backup to ensure continuous operation. The evaporative condensers consist of rows of tubes on the inside of the tower. The tower water cascades downward to directly contact the condenser tubes leaving a scale deposit if the water significantly exceeds the normal operating levels of about 180 ppm SiO2 and about 480 ppm (maximum) M-alkalinity. The original treatment used HEDP, benzotriazole and polymaleic acid with a supplemental feed of polyacrylic acid. Problem: The makeup water typically had 90-110 ppm SiO2, allowing only about 2 cycles of concentration. Due to severe drought conditions in this area for the previous 5 years, water was not readily available and had to be reused to the maximum extent possible. Solution: In 1991, the polymaleic acid and polyacrylic acid scale inhibitors used in the old treatment were replaced with an equal weight of ACUMER 5000 (akumer 5000) (akümer 5000) polymer. The treatment was fed to maintain the same levels as before, but the bleedoff was reduced. Results: With ACUMER 5000 (akumer 5000) (akümer 5000) polymer, the system maintained up to about 4 cycles of concentration without scale or corrosion. Recirculation water has up to 300 ppm total silica and about 650 ppm M-alkalinity (maximum). Benefits of the reduction in bleedoff include: • A calculated 30% reduction in water usage under typical conditions. • A calculated 30% reduction in chemical usage. • An increase in holding time which allows the biocide to work more effectively (since the makeup water has a high organism count). Scale Problem Eliminated at Ice-Making Plant System An ice-making plant with a refrigeration capacity of 270 tons had a history of Description: scale problems, especially on the condenser coils. Silica levels in the makeup water were 46 ppm SiO2. System temperature ranged between 83°F (28°C) and 91°F (33°C). Problem: The water was treated with an all-organic program which left heavy deposits of silica. A thorough cleaning with ammonium bifluoride and hydrochloric acid was performed in the summer of 1992 to remove the heavy deposits. Between August and November of 1992, the COC were maintained at low levels (less than 2) to prevent silica scale. Under these conditions, CaCO3 still formed on the condenser coils, with head pressure on the condenser side measuring approximately 230 psi. Solution: ACUMER 5000 (akumer 5000) (akümer 5000) polymer was added to the system to maintain 15 ppm active polymer in the recirculationg water, and COC were gradually increased to 6 to 9. Results: By February of 1993, head pressure had dropped to the lowest level, 215 psi, indicating no scale. Theoretical silica levels approached 400 ppm SiO2. Ten months after changing the formulation to one containing ACUMER 5000 (akumer 5000) (akümer 5000) polymer, the plant continued to operate without problems. OTHER APPLICATIONS of ACUMER 5000 (akumer 5000) (akümer 5000) Boilers of ACUMER 5000 (akumer 5000) (akümer 5000) The superior hydrothermal stability of ACUMER 5000 (akumer 5000) (akümer 5000) polymer enables its use for controlling magnesium silicate scale in boilers operating up to about 600 psig (42 kg/cm2). Above 600 psig, it is recommended that the silica be removed from the feedwater by external treatment such as ion exchange. Reverse Osmosis The ability of ACUMER 5000 (akumer 5000) (akümer 5000) polymer to disperse colloidal silica as well as other particulates makes it suitable in formulations for fouling prevention in RO membranes used to treat high-silica water. Water Analysis of ACUMER 5000 (akumer 5000) (akümer 5000): Cycles of (at steady state) Makeup Recirculating Concentration pH 7.8-8.1 8.9-9.0 — Conductivity, µmho 330-360 1000-1030 2.9 M-Alkalinity, as CaCO3 154-180 536-540 3.2 Ca, as CaCO3 60-80 236-264 3.6 Mg, as CaCO3 56-80 260-268 3.9 Silica, as SiO2 60-70 265-300 4.2 TOXICITY of ACUMER 5000 (akumer 5000) (akümer 5000) Toxicity data on ACUMER 5000 (akumer 5000) (akümer 5000) silica control polymer are presented in Table 7. SAFE HANDLING INFORMATION ACUMER 5000 (akumer 5000) (akümer 5000) Caution: For Industrial Use Only! Keep Out of Reach of Children! Wear chemical splash goggles and impervious gloves when handling. An approved respirator, suitable for the concentrations encountered, should be worn. FIRST AID INFORMATION of ACUMER 5000 (akumer 5000) (akümer 5000) Skin Contact Wash affected skin area thoroughly with soap and water. Consult a physician if irritation persists. Eye Contact Flush eye immediately with plenty of water for at least 15 minutes. Consult a physician if irritation persists. Inhalation Move victim to fresh air. Ingestion If victim is conscious, dilute product by giving 2 glasses of water to drink and then call a physician. If victim is unconscious, call a physician immediately. Never give an unconscious person anything to drink. MATERIAL SAFETY DATA SHEETS of ACUMER 5000 (akumer 5000) (akümer 5000) Rohm and Haas Company maintains Material Safety Data Sheets (MSDS) on all of its products. These contain important information that you may need to protect your employees and customers against any known health and safety hazards associated with our products. We recommend you obtain copies of MSDS for our products from your local Rohm and Haas technical representative or the Rohm and Haas Company. In addition, we recommend you obtain copies of MSDS from your suppliers of other raw materials used with our product. Under the OSHA Hazard Communication Standard, workers must have access to and understand MSDS on all hazardous substances to which they are exposed. Thus, it is important that appropriate training and information be provided to all employees and that MSDS be available on any hazardous products in their workplace. ACUMER 5000 (akumer 5000) (akümer 5000) Silica and Magnesium Silicate Scale Inhibitor Description of ACUMER 5000 (akumer 5000) (akümer 5000) Rohm and Haas ACUMER 5000 (akumer 5000) (akümer 5000) is a superior scale inhibitor and dispersant for silica and magnesium silicate in recirculating cooling circuits and boilers. Used of ACUMER 5000 (akumer 5000) (akümer 5000) in Water Treatment ACUMER 5000 (akumer 5000) (akümer 5000) Cooling waters ACUMER 5000 (akumer 5000) (akümer 5000) Boilers ACUMER 5000 (akumer 5000) (akümer 5000) Industrial reverse osmosis ACUMER 5000 (akumer 5000) (akümer 5000) Pools and fountains ACUMER 5000 (akumer 5000) (akümer 5000) Advantages of ACUMER 5000 (akumer 5000) (akümer 5000) Prevent the formation of deposits on heat transfer surfaces Prevent inorganic and sedimentation fouling Effectively inhibits magnesium silicate Excellent silica dispersant Outstanding iron, phosphate scale inhibitor Stabilizes corrosion inhibitors Boiler sludge dispersant Typical Properties These properties are typical but do not constitute specifications. Appearance Dark yellow to brown clear solution* Average Molecular weight 5,000 (Mw) % Total Solids 45 % Active Solids 42 pH as is (at 25°C) 2.May Bulk density (at 25°C) 1.Şub Viscosity Brookfield (mPa.s/cps at 25°C) 400 Neutralization 0.13g of NaOH (100%) per g of ACUMER 5000 (akumer 5000) (akümer 5000) *A slight haze may appear; this does not affect the intrinsic properties of the product or its performance. Chemistry and Mode of Action ACUMER 5000 (akumer 5000) (akümer 5000) is a proprietary multifunctional polymer with a molecular weight of 5000 that provides outstanding silica and magnesium silicate scale inhibition. ACUMER 5000 (akumer 5000) (akümer 5000) prevents silica-based scale formation by dispersing colloidal silica and by preventing magnesium silicate scale formation at heat transfer surfaces. Performance of ACUMER 5000 (akumer 5000) (akümer 5000) Control of silica-based scale is a complex problem due to the many forms of silica species that exist: Molybdate-reactive silica: frequently referred to as dissolved silica. Colloidal silica: polymerized silica particles of 0.1 microns or less. Silica scale: primarily magnesium silicate, but may also be iron or calcium silicate. Colloidal silica can dissolve to form silicate in the high temperature/high pH environment near a corroding cathodic surface where dissolved oxygen is reduced to hydroxide ions. These freshly formed silicate anions, added to the dissolved silica already present, can then form magnesium silicate scale (MgSiO3). In addition, colloidal silica alone can co-precipitate with magnesium hydroxide to form a scale of magnesium silicate having non-stoichiometric ratios of magnesium to silica. Normally, if silica levels exceed about 180 ppm SiO2 in the recirculation water of a cooling circuit, severe scaling can occur on heat transfer surfaces. Moreover, the scale that forms is frequently difficult or impossible to remove by conventional means. ACUMER 5000 (akumer 5000) (akümer 5000) has been evaluated under field conditions, allowing up to 300 ppm silica in the recirculating water without scale. Case histories are available upon request from your local technical representative. Applications of ACUMER 5000 (akumer 5000) (akümer 5000) Recirculating cooling circuits ACUMER 5000 (akumer 5000) (akümer 5000) offers unique features for the treatment of silica-limited cooling waters, allowing up to at least 300 ppm silica in the recirculating water without scale or corrosion problems Boilers ACUMER 5000 (akumer 5000) (akümer 5000) The superior hydrothermal stability of ACUMER 5000 (akumer 5000) (akümer 5000) enables its use for controlling magnesium silicate scale in boilers operating up to about 900 psig, although silica may carry over in steam at > 600 psig. Benefits of ACUMER 5000 (akumer 5000) (akümer 5000) Keeps surfaces clean for maximum heat transfer and enhances the performance of organic corrosion inhibitors. Has excellent thermal and chemical stability. Can be formulated at any pH without degradation. Exhibits a very good stability in the presence of hypochlorite. Contains no phosphorus, making its use acceptable where legislation requires that discharge waters contain low or no phosphorus. Chemistry and Mode of Action ACUMER 5000 (akumer 5000) (akümer 5000) is a proprietary multifunctional polymer with a molecular weight of 5000 that provides exceptional silica and magnesium silicate scale inhibition. ACUMER 5000 (akumer 5000) (akümer 5000) helps prevent silica-based scale formation by dispersing colloidal silica and by minimizing magnesium silicate scale formation at heat transfer surfaces. Performance Control of silica-based scale is a complex problem due to the many forms of silica species that exist: • Molybdate-reactive silica: frequently referred to as dissolved silica. • Colloidal silica: polymerized silica particles of 0.1 microns or less. • Silica scale: primarily magnesium silicate, but may also be iron or calcium silicate. Colloidal silica can dissolve to form silicate in the high temperature/high pH environment near a corroding cathodic surface where dissolved oxygen is reduced to hydroxide ions. These freshly formed silicate anions, added to the dissolved silica already present, can then form magnesium silicate scale (MgSiO3). In addition, colloidal silica alone can co-precipitate with magnesium hydroxide to form a scale of magnesium silicate having non-stoichiometric ratios of magnesium to silica. Normally, if silica levels exceed about 180 ppm SiO2 in the recirculation water of a cooling circuit, severe scaling can occur on heat transfer surfaces. Moreover, the scale that forms is frequently difficult or impossible to remove by conventional means. ACUMER 5000 (akumer 5000) (akümer 5000) has been evaluated under field conditions, allowing up to 300 ppm silica in the recirculating water without scale. Case histories are available upon request from your local technical representative. ACUMER 5000 (akumer 5000) (akümer 5000) Silica and Magnesium Silicate Scale Inhibitor / Dow Coating Materials Applications of ACUMER 5000 (akumer 5000) (akümer 5000) • Recirculating cooling circuits ACUMER 5000 (akumer 5000) (akümer 5000) offers distinct features for the treatment of silica-limited cooling waters, allowing up to at least 300 ppm silica in the recirculating water without scale or corrosion problems. • Boilers The excellent hydrothermal stability of ACUMER 5000 (akumer 5000) (akümer 5000) makes it an ideal choice for use in controlling magnesium silicate scale in boilers operating up to about 900 psig, although silica may carry over in steam at >600 psig. Benefits of ACUMER 5000 (akumer 5000) (akümer 5000) • Helps keep surfaces clean for maximum heat transfer and enhances the performance of organic corrosion inhibitors. • Has excellent thermal and chemical stability. • Can be formulated at any pH without degradation. • Exhibits a very good stability in the presence of hypochlorite. • Contains no phosphorus, making its use acceptable where legislation requires that discharge waters contain low or no phosphorus. Description of ACUMER 5000 (akumer 5000) (akümer 5000) ACUMER 5000 (akumer 5000) (akümer 5000) is a superior scale inhibitor and dispersant for silica and magnesium silicate in recirculating cooling circuits and boilers. Advantages of ACUMER 5000 (akumer 5000) (akümer 5000) Effectively inhibits magnesium silicate Excellent silica dispersant Outstanding iron, phosphate scale inhibitor Stabilizes corrosion inhibitors Boiler sludge dispersant Prevents the formation of deposits on heat transfer surfaces Prevents inorganic and sedimentation fouling Properties of ACUMER 5000 (akumer 5000) (akümer 5000): IR-5000 carboxylate-sulfonate copolymer (similar to ACUMER 5000 (akumer 5000) (akümer 5000)) is a superior scale inhibitor and dispersant. It has good inhibition for silica and magnesium silicate when used in recirculation cooling circuits and boilers. It is a superior phosphate scale inhibitor for dry or hydrated ferric oxide. Acting as a rust inhibitor, IR-5000 can also be used in systems like Industrial RO, pools, and fountains, etc. (Similar to ACUMER 5000 (akumer 5000) (akümer 5000)) Synthetic magnesium silicates (ACUMER 5000 (akumer 5000) (akümer 5000)) are white, odorless, finely divided powders formed by the precipitation reaction of water-soluble sodium silicate (water glass) and a water-soluble magnesium salt such as magnesium chloride, magnesium nitrate or magnesium sulfate. The composition of the precipitate depends on the ratio of the components in the reaction medium, the addition of the correcting substances, and the way in which they are precipitated.[1][2][3] The molecular formula is typically written as MgO:XSiO2, where X denotes the average mole ratio of SiO2 to MgO. The product is hydrated and the formula is sometimes written MgO:XSiO2•H2O to show the water of hydration. Properties of ACUMER 5000 (akumer 5000) (akümer 5000) Unlike natural magnesium silicates like talc and forsterite olivine which are crystalline, synthetic magnesium silicates are amorphous.[1] Synthetic magnesium silicates are insoluble in water or alcohol.[4] The particles are usually porous, and the BET surface area can range from less than 100 m2/g to several hundred m2/g.
ACUSOL 820
DESCRIPTION:
When neutralized to a pH above 7 by adding alkalis, ACUSOL 820 polymer thickens instantly.
The instantaneous effect on viscosity and easy incorporation of ACUSOL 820 polymer into alkaline cleaner formulations offer savings in valuable production time that cannot be matched by carbomer or cellulosic thickeners, requiring predissolution and elimination of lumps.
ACUSOL 820 can also thicken solutions containing high levels of surfactants at low pH.

CAS NUMBER: 75760-37-1
TRADE NAME: Acusol 820
GENERIC NAME: Hydrophobically modified Alkali Soluble acrylic polymer Emulsion (HASE)

ACUSOL 820 has High aqueous thickening and stabilizing for cleaning formulations
From glass cleaners to liquid laundry detergents to oven cleaners, ACUSOL 820 Rheology Modifier/Stabilizer is very cost-effective and provides unusually high aqueous thickening and stabilizing properties.
When neutralized to a pH above 7, ACUSOL 820 Rheology Modifier/Stabilizer allows viscosity build of various formulations, offering savings in production time that cannot be matched by carbomer or cellulosic thickeners.

ACUSOL 820 Rheology Modifier/Stabilizer can also thicken solutions containing high levels of surfactants.
ACUSOL 820 is Rheology Modifier and Stabilizer
ACUSOL 820 is a Hydrophobically modified AlkaliSoluble acrylic polymer Emulsion (HASE) with unusually high aqueous thickening andstabilising efficiency.

Working by association, ACUSOL 820 can also thicken solutions containing high levels of surfactants at low pH.
This unique performance is achieved by acidifying a neutralized surfactant-containing formulation with a dilute organic or mineral acid.

Acusol 820 is a hydrophobically modified Alkali Soluble acrylic polymer emulsion with unusually high aqueous thickening and stabilizing efficiency.
When neutralized to a ph above 7 ACUSOL 820 thickens instantly.
This characteristic has led to its incorporation into alkaline cleaner formulations such as glass and emulsion cleaners, hand dishwash liquid detergents, hard surface and floor cleaners, liquid abrasive cleaners, liquid laundry detergents, oven cleaner, pain strippers waterless cleaners and white-wall tire cleaners.

USES OF ACUSOL 820:
ACUSOL 820 is used in All-purpose cleaners
ACUSOL 820 is used in Floor cleaners
ACUSOL 820 is used in Hand dishwashing liquids

ACUSOL 820 is used in Laundry detergents
ACUSOL 820 is used in Automatic dishwashing gels
ACUSOL 820 is used in Oven cleaners
ACUSOL 820 is used in Abrasive Cleaners
ACUSOL 820 is used in Alkaline Cleaner
ACUSOL 820 is used in Alkaline Paint Strippers

ACUSOL 820 is used in Caustic Soda Thickener
ACUSOL 820 is used in Dishwash Detergents
ACUSOL 820 is used in Drain Cleaner

ACUSOL 820 is used in Floor Cleaners
ACUSOL 820 is used in Glass Cleaners
ACUSOL 820 is used in Hand Dishwash Detergents

ACUSOL 820 is used in Hard Surface Cleaners
ACUSOL 820 is used in Laundry Detergents
ACUSOL 820 is used in Paint Strippers

ACUSOL 820 is used in Rheology Modifier
ACUSOL 820 is used in Thickener
ACUSOL 820 is used in Toilet Freshener

ACUSOL 820 is used in Waterless Hand Cleaners
ACUSOL 820 is used in White Wall Tire Cleaner

BENEFITS OF ACUSOL 820:
ACUSOL 820 has Instant thickening capabilities when mixed with any alkali
ACUSOL 820 has Low viscosity for easy handling
ACUSOL 820 has Water-based polymerization with no residual solvents

ACUSOL 820 is Compatible with high levels of certain salts and electrolytes commonly used in household cleaning formulations
ACUSOL 820 is Convenient, rapid thickening of solutions and gels for an end-product that is free from air bubbles or lumps

ACUSOL 820 is Non-GMO
To the best of our knowledge ACUSOL 820 does not contain ingredients of animal origin.


FEATURES AND BENEFITS OF ACUSOL 820:
Anionic: Can be thickened instantly with any alkali. Compatible with both non-ionic andanionic surfactants, builders and fillers.
Liquid: Supplied as a low viscosity liquid emulsion, it is very easy to handle.
No predissolution, elimination of lumps or warming required.

Associative nature: Association may occur with other formulation components giving enhanced viscosity and stability.

Rheology: Gives pseudoplastic (shear thinning) rheology, similar to cellulosics but maintains higher viscosity for higher shear rates.

Emulsion technology: Water-based polymerization.
No residual solvents.
No residual organic initiators.
Instant neutralization: Permits continuous manufacturing process through in-line static mixers.

Gel appearance: Gives clear gels or solutions.
Microbial resistance: Being a synthetic polymer, ACUSOL 820 Rheology Modifier/Stabilizer is inherently resistant to microbes and enzymes that can degrade cellulosic thickeners, leading to loss of viscosity.
Salt tolerance: Compatible with high levels of salts and electrolytes commonly used in household and institutional formulations.


GENERAL MIXING PROCEDURE OF ACUSOL 820:
Operating flexibility is provided by the physical characteristics of the product (low viscosity liquid before neutralization), and its high thickening efficiency allows varying operating procedures.

The following mixing procedure meets most formulating needs:
1. Introduce ACUSOL 820 polymer into the formulation water.
This should provide at least a threefold dilution of the polymer.
2. Add the nonionic surfactants (if any).
3. Add the anionic surfactants (if any)—low pH first.*
4. Add builders, fillers, particulates.
5. Add dyes, then perfume.
6. Neutralize with the chosen alkali



SAFETY INFORMATION ABOUT ACUSOL 820:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product


CHEMICAL AND PHYSICAL PROPERTIES OF ACUSOL 820:
Appearance:
Physical state liquid
Color white milky
Odor: Mild odor
pH 2.2 - 3.2
Melting point/range 0 °C Water
Boiling point (760 mmHg) 100.00 °C Water
Flash point: Noncombustible
Evaporation Rate (Butyl Acetate= 1)
Vapor Pressure 17.0000000 mmHg at 25.00 °C Water
Relative Vapor Density (air = 1) Relative Density (water = 1) 1.0000 - 1.2000
Dynamic Viscosity 40.000 mPa.s
Percent volatility 69.00 - 71.00 % Water



Ada Çayı Ekstraktı
Salvia Officinalis Extract ; extract of the whole plant the sage, salvia officinalis l., lamiaceae; extrapone sage (Symrise); common sage extract; garden sage extract cas no:8022-56-8
ADBAC - Alkyl Dimethyl Benzyl Ammonium Chloride
1,4-Butanedicarboxylic acid; 1,6-Hexanedioic Acid; Adipinic Acid; Acifloctin; Acinetten; Hexanedioic acid; 1,4-BUTANEDICARBOXYLIC ACID; 1,6-HEXANEDIOIC ACID; ADIPIC ACID; adipinic acid; AKOS BBS-00004308; BUTANE-1,4-DICARBOXYLIC ACID; DICARBOXYLIC ACID C6; FEMA 2011; HEXANDIOIC ACID; RARECHEM AL BO 0180; acideadipique; Acifloctin; Acinetten; Adilactetten; adipate; adipic; Adipinsαure; Adi-pure; ai3-03700; femanumber2011 CAS NO:124-04-9
ADDOCAT 10/9
Addocat 10/9 also shortens the pot life of the formulation.
Addocat 10/9 is suitable for use in polyurethane coatings.


Product Type: Catalysts / Accelerators / Initiators > Amines
Chemical Composition: Aminoalkanol ester (ester amine)
Physical Form: Liquid, Colorless to brown


Addocat 10/9 is an aminoalkanol ester (ester amine).
Addocat 10/9 acts as a catalyst.
Addocat 10/9 also shortens the pot-life of the formulation.


To facilitate metering, Addocat 10/9 should be used as a 10% solution in butyl acetate, ethyl acetate, methylisobutyl ketone or methylethyl ketone.
Addocat 10/9 is suitable for use in polyurethane coatings.
Recommended dosage level of Addocat 10/9 is 0.1-0.5%.


Addocat 10/9 has a shelf life of 6 months.
Addocat 10/9 is a mild catalyst for polyurethane coatings, if aromatic isocyanates like Desmodur L are used.
Addocat 10/9 accelerates the drying and curing of polyurethane coatings.


Addocat 10/9 also shortens the pot life of the formulation.
Addition: 0.1 - 0.5% Addocat 10/9, calculated on the formulations isocyanate / polyol content.



USES and APPLICATIONS of ADDOCAT 10/9:
Addocat 10/9 cts as a catalyst.
Addocat 10/9 also shortens the pot-life of the formulation.
To facilitate metering, Addocat 10/9 should be used as a 10% solution in butyl acetate, ethyl acetate, methylisobutyl ketone or methylethyl ketone.


Addocat 10/9 is suitable for use in polyurethane coatings.
To facilitate metering, Addocat 10/9 should be used as a 10% solution in butyl acetate, ethyl acetate, methylisobutyl ketone or methylethyl ketone.
Addocat 10/9 is used water content of the solving agent should be less than 0.05 pbw.


Storage of solutions of Addocat 10/9 should be proofed first ock foam and hot-molded foam.
Addocat 10/9 is also used for HR foam and, as a co-catalyst, for rigid foams.
Addocat 10/9 is used amino-alkanol esters, reaction accelerators in polyurethane coatings



FUNCTION OF ADDOCAT 10/9:
Catalyst for polyurethane coatings.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 10/9:
Tradename: ADDOCAT 10/9
Generic name: ADDITIVE FOR POLYURETHANES
Product Type: Catalysts / Accelerators / Initiators > Amines
Chemical Composition: Aminoalkanol ester (ester amine)
Physical Form: Liquid, Colorless to brown



FIRST AID MEASURES of ADDOCAT 10/9:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 10/9:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 10/9:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 10/9:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 10/9:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 10/9:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

ADDOCAT 102
Addocat 102, a chemical with molecular formula C4H6N2, is mainly used for deoxyribonucleic acid synthesis use.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.
Addocat 102 acts as a crosslinking catalyst.


CAS Number: 616-47-4
EC Number: 210-484-7
MDL Number: MFCD00005292
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical Composition: 1-methylimidazole
Molecular Formula: C4H6N2



SYNONYMS:
Tertiary amine, Dabco 33-S, Dabco 33S, 33% BDO triethylenediamine solution, Addocat 106, TEDA-L33B, DABCO POLYCAT microporous catalyst, microporous catalyst, gel catalyst Dabco 33S, 1-Methylimidazole, Cap B (1-methylimidazole 16% in THF), Cap B (1-methylimidazole 10% in THF), Cap B (1-methylimidazole 12% in acetonitrile/ pyridine 78 : 10), 1-methyl- 1H-imidazole, methyl imidazole, N-Methylimidazole, N-methyl imidazole, 1-Methyl-1H-imidazole, Thiamazole Imp. B (EP), Thiamazole Impurity B, N-METHYLIMIDAZOLE, 1-methyl-1h-imidazole, MIM, MeIm, methyl imidazole, 1H-Imidazole, 1-methyl-, N-methylimidazole (1-methylimidazole), 1-methylmidazole, N-methyl midazole, N-methyl glyoxaline, 1-Methyl-1H-imidazole, N-Methylimidazole, 1H-Imidazole, 1-methyl-, 1-methyl-1h-imidazole, 1-METHYLIMIDAZOLE, LUPRAGEN(R) NMI, methyl imidazole, N-METHYLIMIDAZOLE, 1-methyl-1h-imidazol, 1-methyl-imidazol, Imidazole, 1-methyl-, N-methylimidazole (1-methylimidazole), N-methyl midazole, N-methyl glyoxaline, CAP B (1-METHYLIMIDAZOLE 12% IN ACETONIT, 1-Methylimidazole, >=99%, purified by redistillation, CAP B (1-METHYLIMIDAZOLE 10% IN THF), CAP B (1-METHYLIMIDAZOLE 10% IN, CAP B (1-METHYLIMIDAZOLE 16% IN THF), 1-METHYLIMIDAZOLE, FOR DNA SYNTHESIS, 1-Methylimdazole, 1H-Imidazole, 1-methyl-, 1-methylimidazole solution, 1-methylimidazole, 1-Methyl-1H-imidazole, 616-47-7, N-Methylimidazole, 1H-Imidazole, 1-methyl-, IMIDAZOLE, 1-METHYL-, N-methylimidazol, 1-methylimidazol, n-methyl imidazole, MFCD00005292, DTXSID6052291, CHEBI:113454, P4617QS63Y, NSC-88064, 1-methyl-imidazole, 1-methylimdazole, EINECS 210-484-7, N1-Methylimidazole, UNII-P4617QS63Y, Araldite DY 070, NSC 88064, 3-methylimidazole, N-methyl-imidazol, N-methyl-imidazole, 1-methyl imidazole, 1-N-methylImidazole, Lopac-M-8878, 1-methyl-(1H)-imidazole, CHEMBL543, 1-Methyl-1H-imidazole #, EC 210-484-7, WLN: T5N CNJ A1, Lopac0_000831, 3-methyl-1H-imidazol-3-ium, BDBM7884, DTXCID6030863, HMS3262H03, BCP29437, NSC88064, STR00990, Tox21_304006, Tox21_500831, BBL011447, STL146559, AKOS000119840, CCG-204915, CS-W008580, LP00831, PS-9372, SDCCGSBI-0050808.P002, NCGC00015702-01, NCGC00015702-02, NCGC00015702-03, NCGC00015702-04, NCGC00094162-01, NCGC00094162-02, NCGC00261516-01, NCGC00357222-01, 1-Methylimidazole, ReagentPlus(R), 99%, 1-Methylimidazole, redistilled from glass, CAS-616-47-7, PD015169, DB-002020, THIAMAZOLE IMPURITY B [EP IMPURITY], EU-0100831, M0508, NS00009025, EN300-21628, 1-Methylimidazole, puriss., >=99.0% (GC), D70869, M 8878, 1-Methylimidazole, Vetec(TM) reagent grade, 98%, SR-01000076013, Q-200126, Q4545792, SR-01000076013-1, 1-Methylimidazole, >=99%, purified by redistillation, F0001-1635, Z104506032, InChI=1/C4H6N2/c1-6-3-2-5-4-6/h2-4H,1H, Cap B (1-methylimidazole 16% in THF), for oligonucleotide synthesis, filtered through a 1µm filter, Capping B (10 % N-methylimidazole in THF / pyridine, V / V = 80 : 10) NC-0803 emp Biotech GmbH, Capping B, 16 % NMI in THF, emp Biotech GmbH (THF/N-methylimidazole, V / V = 84 : 16) NC-0801, 450ml : 28-400 thread, 2.5L : GL45 thread



Addocat 102, also known as N-Methylimidazole, is used as a specialty solvent, a base, and as a precursor to some ionic liquids.
In rigid foams Addocat 102 catalyses mainly the crosslinking reaction (isocyanate-polyol).
For the production of these materials Addocat 102 is used as a co-catalyst in combination with Addocat 726 b, Addocat 104 or Addocat PP.


Addocat 102 gives the rigid foam a tough and elastic skin, thus improving the adhesion of the foam to facings, particularly in sandwich panels.
Addocat 102 is a 1-methylimidazole.
Addocat 102 acts as a crosslinking catalyst.


Addocat 102 gives the rigid foam a tough and elastic skin, thus improving the adhesion of the foam to facings, particularly in sandwich panels.
Addocat 102 is a polyurethane catalyst based on a tertiary amine, specifically N-methylimidazole.
Addocat 102 activates the gelling (cross linking) reaction in rigid polyurethane foams.


Addocat 102 produces tough and elastic skin, thus improving the adhesion of the foam to facings.
Addocat 102, a chemical with molecular formula C4H6N2, is mainly used for deoxyribonucleic acid synthesis use.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.


Addocat 102 is miscible with water.
Addocat 102 is a versatile intermediate with a variety of applications.
Addocat 102 is a versatile intermediate used as a building block for active ingredients as well as in epoxy curing.


Addocat 102 is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Addocat 102 has been enhanced for catalysis.


Addocat 102 is a derivative of imidazole that is utilized in the manufacture of such classes of items as pharmaceuticals, pesticides, ion-exchange resins, dye intermediates, textile auxiliaries, photographic chemicals, and corrosion inhibitors.
Addocat 102 is a 1H-imidazole having a methyl substituent at the N-1 position.


Addocat 102 is a metabolite of 1-methyl-2-thioimidazole (methimazole).
Addocat 102 inhibits bone resorption.
Addocat 102 is a 1H-imidazole having a methyl substituent at the N-1 position.



USES and APPLICATIONS of ADDOCAT 102:
Addocat 102 is used continuous production of sandwich panels.
Addocat 102 is used discontinuous heat/cold insulation of refrigerators and piping.
Addocat 102 is used on-site casting.


Addocat 102 is used for the production of polyurethane foam and discontinuous heat/cold insulation of refrigerators and piping.
Addocat 102 is used Automotive industry Body for electrical equipment Cables Construction Construction material Electronics Industry Housing for Electric and Electronics In-situ foams Pipe insulation Plastic- and Rubberpolymers Polymer auxiliaries


Typically Addocat 102 is used in the continuous production of sandwich panels, discontinuous hear/cold insulation if refrigerators and piping, and for on-site casting.
Addocat 102 is used auto industry, Electrical machinery equipment, cable, architecture, Building Materials, electronics industry, Electrical and electronic equipment housing, In-situ foam, Pipeline insulation, Plastic and rubber polymers, and Polymer Additives.


Addocat 102 is a heat-sensitive moderately active gel-like catalyst, etc.
Addocat 102 is mainly used in polyurethane semi-rigid foam, microcellular elastomers and so on;
Addocat 102 can be used as an epoxy curing accelerator with anhydride curing agents in epoxy potting adhesives.


Addocat 102 is used for deoxyribonucleic acid synthesis. Hydroxyacetylation catalyst.
Addocat 102 is mainly used as curing agent for epoxy resin and other resins.
Addocat 102 is used in the fields of casting, bonding and FRP.


Addocat 102 is used organic synthesis intermediates and resin curing agent and adhesive.
Addocat 102 can be used in the fields of casting, bonding and glass fiber reinforced plastic.
Addocat 102 is used as organic synthesis intermediates and resin curing agent, adhesive, etc.


In rigid foams Addocat 102 catalyses mainly the crosslinking reaction (isocyanate-polyol).
For the production of these materials Addocat 102 is used as a co-catalyst in combination with Addocat 726 b, Addocat 104 or Addocat PP.


Addocat 102 gives the rigid foam a tough and elastic skin,
thus improving the adhesion of the foam to facings, articularly in sandwich panels.
Addocat 102 is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Ther release to the environment of Addocat 102 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).
Release to the environment of Addocat 102 can occur from industrial use: formulation of mixtures.


Addocat 102 is used in the following products: coating products, pharmaceuticals, polymers and oil and gas exploration or production products.
Addocat 102 is used for the manufacture of: chemicals and plastic products.
Release to the environment of Addocat 102 can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, as processing aid and for thermoplastic manufacture.


Release to the environment of Addocat 102 can occur from industrial use: manufacturing of the substance.
Addocat 102 is used as a precursor for the synthesis of pyrrole-imidazole polyamides, ionic liquids such as 1-butyl-3-methylimidazolium hexafluorophosphate.
Addocat 102 is actively involved in removing acid during the production of diethoxyphenylphosphine.


Addocat 102 is used as an intermediate in organic synthesis.
Addocat 102 is a derivative of imidazole used in the production of pharmaceuticals, pesticides, ion exchange resins, dye intermediates, textile auxiliaries, photographic chemicals, and corrosion inhibitors.


Addocat 102 can also be used as a catalyst for the manufacture of polyurethane and a curing agent for epoxy resins.
For example, when Addocat 102 is added to an aqueous diethylenetriamine (DETA) solution, high CO2 loading can be achieved through phase separation of the absorbent during CO2 absorption.


Addocat 102 is also used as a catalyst for manufacturing polyurethanes and a curing agent for epoxy resins.
Addocat 102 is an aprotic solvent.


-Applications of Addocat 102:
*Continuous production of sandwich panels.
*Discontinuous heat/cold insulation of refrigerators and piping.
*On-site casting.



CHEMICAL PROPERTIES OF ADDOCAT 102:
Addocat 102 is an aromatic heterocyclic organic compound with the formula C4H6N2.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.
Addocat 102 is miscible with water.

Addocat 102 is an important raw material for the synthesis of pharmaceutical intermediates, used in the preparation of losartan, nizofenone, 1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride and naphazoline hydrochloride, etc.
Addocat 102 is also used as a specialty solvent, a base, and as a precursor to some ionic liquids.



PREPARATION OF ADDOCAT 102:
Addocat 102 is prepared mainly by two routes industrially.
The main one is acid-catalysed methylation of imidazole by methanol.

The second method involves the Radziszewski reaction from glyoxal, formaldehyde, and a mixture of ammonia and methylamine.
(CHO)2 + CH2O + CH3NH2 + NH3 → H2C2N(NCH3)CH + 3 H2O
Addocat 102 can be synthesized on a laboratory scale by methylation of imidazole at the pyridine-like nitrogen and subsequent deprotonation.

Similarly, Addocat 102 may be synthesized by first deprotonating imidazole to form a sodium salt followed by methylation.
H2C2N(NH)CH + CH3I → [H2C2(NH)(NCH3)CH]I
[H2C2(NH)(NCH3)CH]I + NaOH → H2C2N(NCH3)CH + H2O + NaI



FUNCTION OF ADDOCAT 102:
Catalyst for the production of rigid polyurethane foam.



DOSAGE OF ADDOCAT 102:
0.5 - 1.0 p.b.w. Addocat 102, calculated on 100 p.b.w. polyol, together with 1 - 3 p.b.w Addocat PP or Addocat 726 b or 0.3 - 1.0 p.b.w. Addocat 104.



STORAGE AND TRANSPORTATION OF ADDOCAT 102:
Addocat 102 should be sealed and stored in dry, cool and ventilated warehouse, filled with nitrogen and sealed in a cool and dry place for storage.



PURIFICATION METHODS OF ADDOCAT 102:
Dry Addocat 102 with sodium metal and then distil it.
Store Addocat 102 at 0o under dry argon.
The picrate has m 159.5-160.5o (from H2O).



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 102:
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical Composition: 1-methylimidazole
Physical Form: Liquid
Chemical Composition: Tertiary amine
Physical Form: Clear, colorless to pale yellow liquid
Density (20 °C): Approx. 1.03 g/cm³
Viscosity (25 °C): Approx. 2 mPa.s
Boiling Point: 198 °C
Solidification Point: Approx. -2 °C
Flash Point: 92 °C (ASTM-D 93, DIN EN 22719)
Miscibility with Water: Miscible

Water Content: Max. 0.5%
Substance Content: Min. 99.0%
Relative Density: 1.030
Refractive Index: 1.4970
Flash Point (℃): 92
Melting Point (°C): -60
Boiling Point (°C): 198
Appearance: Colorless transparent liquid
Content: ≥99%
Density: 1.03 g/mL at 25 ℃
Vapor Pressure: 0.4 mm Hg (20 ℃)
Color: Clear colorless to yellow

Specific Gravity: 1.031
pKa: 6.95 (at 25℃)
BRN: 105197
Storage Temp.: Store below +30°C
Refractive Index: n20/D 1.495 (lit.)
Form: Liquid
pH Range: 9.5 - 11.5 at 100 g/L at 20 °C
pH: 9.5-10.5 (50 g/L, H2O, 20℃)
InChIKey: MCTWTZJPVLRJOU-UHFFFAOYSA-N
Explosive Limit: 2.7-15.7% (V)
Fp: 198 °F
Vapor Pressure: 0.4 mm Hg (20 °C)
EPA Substance Registry System: 1H-Imidazole, 1-methyl- (616-47-7)
Density: 1.03 g/mL at 25 °C (lit.)
Water Solubility: Miscible with water

Melting Point: −60 °C (lit.)
Stability: Stable, but moisture sensitive.
Incompatible with acids, acid anhydrides, strong oxidizing agents,
moisture, carbon dioxide, acid chlorides.
Sensitive: Hygroscopic
NIST Chemistry Reference: 1H-Imidazole, 1-methyl- (616-47-7)
CAS DataBase Reference: 616-47-7 (CAS DataBase Reference)
Molecular Weight: 82.10 g/mol
XLogP3: -0.1
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 82.053098200 g/mol
Monoisotopic Mass: 82.053098200 g/mol
Topological Polar Surface Area: 17.8 Ų

Heavy Atom Count: 6
Formal Charge: 0
Complexity: 44.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Purity / Analysis Method: >99.0% (GC)
Molecular Formula: C4H6N2
Molecular Formula / Molecular Weight: C4H6N2 = 82.11
Physical State (20 °C): Liquid

Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas: Store under inert gas
Condition to Avoid: Air Sensitive, Hygroscopic
CAS RN: 616-47-7
Reaxys Registry Number: 105197
PubChem Substance ID: 87572549
SDBS (AIST Spectral DB): 3569
MDL Number: MFCD00005292
CB Number: CB1316726
MOL File: 616-47-7.mol
Melting Point: −60 °C (lit.)
Boiling Point: 198 °C (lit.)
Density: 1.03 g/mL at 25 °C (lit.)

Vapor Pressure: 0.4 mm Hg (20 °C)
Refractive Index: n20/D 1.495 (lit.)
Flash Point: 198 °F
Storage Temp.: Store below +30°C
Solubility: Chloroform (Slightly), Methanol (Slightly)
Form: Liquid
pKa: 6.95 (at 25°C)
Specific Gravity: 1.031
Color: Clear colorless to yellow
pH: 9.5-10.5 (50 g/L, H2O, 20°C)
pH Range: 9.5 - 11.5 at 100 g/L at 20 °C
Explosive Limit: 2.7-15.7% (V)

Water Solubility: Miscible with water
Sensitive: Hygroscopic
BRN: 105197
Stability: Stable, but moisture sensitive.
Incompatible with acids, acid anhydrides, strong oxidizing agents,
moisture, carbon dioxide, acid chlorides
InChIKey: MCTWTZJPVLRJOU-UHFFFAOYSA-N
LogP: -0.19 at 25°C
CAS DataBase Reference: 616-47-7
EWG's Food Scores: 1
FDA UNII: P4617QS63Y
NIST Chemistry Reference: 1H-Imidazole, 1-methyl- (616-47-7)
EPA Substance Registry System: 1H-Imidazole, 1-methyl- (616-47-7)



FIRST AID MEASURES of ADDOCAT 102:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 102:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 102:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 102:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 102:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 102:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 102
Addocat 102, a chemical with molecular formula C4H6N2, is mainly used for deoxyribonucleic acid synthesis use.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.
Addocat 102 acts as a crosslinking catalyst.


CAS Number: 616-47-4
EC Number: 210-484-7
MDL Number: MFCD00005292
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical Composition: 1-methylimidazole
Molecular Formula: C4H6N2



SYNONYMS:
Tertiary amine, Dabco 33-S, Dabco 33S, 33% BDO triethylenediamine solution, Addocat 106, TEDA-L33B, DABCO POLYCAT microporous catalyst, microporous catalyst, gel catalyst Dabco 33S, 1-Methylimidazole, Cap B (1-methylimidazole 16% in THF), Cap B (1-methylimidazole 10% in THF), Cap B (1-methylimidazole 12% in acetonitrile/ pyridine 78 : 10), 1-methyl- 1H-imidazole, methyl imidazole, N-Methylimidazole, N-methyl imidazole, 1-Methyl-1H-imidazole, Thiamazole Imp. B (EP), Thiamazole Impurity B, N-METHYLIMIDAZOLE, 1-methyl-1h-imidazole, MIM, MeIm, methyl imidazole, 1H-Imidazole, 1-methyl-, N-methylimidazole (1-methylimidazole), 1-methylmidazole, N-methyl midazole, N-methyl glyoxaline, 1-Methyl-1H-imidazole, N-Methylimidazole, 1H-Imidazole, 1-methyl-, 1-methyl-1h-imidazole, 1-METHYLIMIDAZOLE, LUPRAGEN(R) NMI, methyl imidazole, N-METHYLIMIDAZOLE, 1-methyl-1h-imidazol, 1-methyl-imidazol, Imidazole, 1-methyl-, N-methylimidazole (1-methylimidazole), N-methyl midazole, N-methyl glyoxaline, CAP B (1-METHYLIMIDAZOLE 12% IN ACETONIT, 1-Methylimidazole, >=99%, purified by redistillation, CAP B (1-METHYLIMIDAZOLE 10% IN THF), CAP B (1-METHYLIMIDAZOLE 10% IN, CAP B (1-METHYLIMIDAZOLE 16% IN THF), 1-METHYLIMIDAZOLE, FOR DNA SYNTHESIS, 1-Methylimdazole, 1H-Imidazole, 1-methyl-, 1-methylimidazole solution, 1-methylimidazole, 1-Methyl-1H-imidazole, 616-47-7, N-Methylimidazole, 1H-Imidazole, 1-methyl-, IMIDAZOLE, 1-METHYL-, N-methylimidazol, 1-methylimidazol, n-methyl imidazole, MFCD00005292, DTXSID6052291, CHEBI:113454, P4617QS63Y, NSC-88064, 1-methyl-imidazole, 1-methylimdazole, EINECS 210-484-7, N1-Methylimidazole, UNII-P4617QS63Y, Araldite DY 070, NSC 88064, 3-methylimidazole, N-methyl-imidazol, N-methyl-imidazole, 1-methyl imidazole, 1-N-methylImidazole, Lopac-M-8878, 1-methyl-(1H)-imidazole, CHEMBL543, 1-Methyl-1H-imidazole #, EC 210-484-7, WLN: T5N CNJ A1, Lopac0_000831, 3-methyl-1H-imidazol-3-ium, BDBM7884, DTXCID6030863, HMS3262H03, BCP29437, NSC88064, STR00990, Tox21_304006, Tox21_500831, BBL011447, STL146559, AKOS000119840, CCG-204915, CS-W008580, LP00831, PS-9372, SDCCGSBI-0050808.P002, NCGC00015702-01, NCGC00015702-02, NCGC00015702-03, NCGC00015702-04, NCGC00094162-01, NCGC00094162-02, NCGC00261516-01, NCGC00357222-01, 1-Methylimidazole, ReagentPlus(R), 99%, 1-Methylimidazole, redistilled from glass, CAS-616-47-7, PD015169, DB-002020, THIAMAZOLE IMPURITY B [EP IMPURITY], EU-0100831, M0508, NS00009025, EN300-21628, 1-Methylimidazole, puriss., >=99.0% (GC), D70869, M 8878, 1-Methylimidazole, Vetec(TM) reagent grade, 98%, SR-01000076013, Q-200126, Q4545792, SR-01000076013-1, 1-Methylimidazole, >=99%, purified by redistillation, F0001-1635, Z104506032, InChI=1/C4H6N2/c1-6-3-2-5-4-6/h2-4H,1H, Cap B (1-methylimidazole 16% in THF), for oligonucleotide synthesis, filtered through a 1µm filter, Capping B (10 % N-methylimidazole in THF / pyridine, V / V = 80 : 10) NC-0803 emp Biotech GmbH, Capping B, 16 % NMI in THF, emp Biotech GmbH (THF/N-methylimidazole, V / V = 84 : 16) NC-0801, 450ml : 28-400 thread, 2.5L : GL45 thread



Addocat 102, also known as N-Methylimidazole, is used as a specialty solvent, a base, and as a precursor to some ionic liquids.
In rigid foams Addocat 102 catalyses mainly the crosslinking reaction (isocyanate-polyol).
For the production of these materials Addocat 102 is used as a co-catalyst in combination with Addocat 726 b, Addocat 104 or Addocat PP.


Addocat 102 gives the rigid foam a tough and elastic skin, thus improving the adhesion of the foam to facings, particularly in sandwich panels.
Addocat 102 is a 1-methylimidazole.
Addocat 102 acts as a crosslinking catalyst.


Addocat 102 gives the rigid foam a tough and elastic skin, thus improving the adhesion of the foam to facings, particularly in sandwich panels.
Addocat 102 is a polyurethane catalyst based on a tertiary amine, specifically N-methylimidazole.
Addocat 102 activates the gelling (cross linking) reaction in rigid polyurethane foams.


Addocat 102 produces tough and elastic skin, thus improving the adhesion of the foam to facings.
Addocat 102, a chemical with molecular formula C4H6N2, is mainly used for deoxyribonucleic acid synthesis use.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.


Addocat 102 is miscible with water.
Addocat 102 is a versatile intermediate with a variety of applications.
Addocat 102 is a versatile intermediate used as a building block for active ingredients as well as in epoxy curing.


Addocat 102 is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Addocat 102 has been enhanced for catalysis.


Addocat 102 is a derivative of imidazole that is utilized in the manufacture of such classes of items as pharmaceuticals, pesticides, ion-exchange resins, dye intermediates, textile auxiliaries, photographic chemicals, and corrosion inhibitors.
Addocat 102 is a 1H-imidazole having a methyl substituent at the N-1 position.


Addocat 102 is a metabolite of 1-methyl-2-thioimidazole (methimazole).
Addocat 102 inhibits bone resorption.
Addocat 102 is a 1H-imidazole having a methyl substituent at the N-1 position.



USES and APPLICATIONS of ADDOCAT 102:
Addocat 102 is used continuous production of sandwich panels.
Addocat 102 is used discontinuous heat/cold insulation of refrigerators and piping.
Addocat 102 is used on-site casting.


Addocat 102 is used for the production of polyurethane foam and discontinuous heat/cold insulation of refrigerators and piping.
Addocat 102 is used Automotive industry Body for electrical equipment Cables Construction Construction material Electronics Industry Housing for Electric and Electronics In-situ foams Pipe insulation Plastic- and Rubberpolymers Polymer auxiliaries


Typically Addocat 102 is used in the continuous production of sandwich panels, discontinuous hear/cold insulation if refrigerators and piping, and for on-site casting.
Addocat 102 is used auto industry, Electrical machinery equipment, cable, architecture, Building Materials, electronics industry, Electrical and electronic equipment housing, In-situ foam, Pipeline insulation, Plastic and rubber polymers, and Polymer Additives.


Addocat 102 is a heat-sensitive moderately active gel-like catalyst, etc.
Addocat 102 is mainly used in polyurethane semi-rigid foam, microcellular elastomers and so on;
Addocat 102 can be used as an epoxy curing accelerator with anhydride curing agents in epoxy potting adhesives.


Addocat 102 is used for deoxyribonucleic acid synthesis. Hydroxyacetylation catalyst.
Addocat 102 is mainly used as curing agent for epoxy resin and other resins.
Addocat 102 is used in the fields of casting, bonding and FRP.


Addocat 102 is used organic synthesis intermediates and resin curing agent and adhesive.
Addocat 102 can be used in the fields of casting, bonding and glass fiber reinforced plastic.
Addocat 102 is used as organic synthesis intermediates and resin curing agent, adhesive, etc.


In rigid foams Addocat 102 catalyses mainly the crosslinking reaction (isocyanate-polyol).
For the production of these materials Addocat 102 is used as a co-catalyst in combination with Addocat 726 b, Addocat 104 or Addocat PP.


Addocat 102 gives the rigid foam a tough and elastic skin,
thus improving the adhesion of the foam to facings, articularly in sandwich panels.
Addocat 102 is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Ther release to the environment of Addocat 102 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).
Release to the environment of Addocat 102 can occur from industrial use: formulation of mixtures.


Addocat 102 is used in the following products: coating products, pharmaceuticals, polymers and oil and gas exploration or production products.
Addocat 102 is used for the manufacture of: chemicals and plastic products.
Release to the environment of Addocat 102 can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), as processing aid, as processing aid and for thermoplastic manufacture.


Release to the environment of Addocat 102 can occur from industrial use: manufacturing of the substance.
Addocat 102 is used as a precursor for the synthesis of pyrrole-imidazole polyamides, ionic liquids such as 1-butyl-3-methylimidazolium hexafluorophosphate.
Addocat 102 is actively involved in removing acid during the production of diethoxyphenylphosphine.


Addocat 102 is used as an intermediate in organic synthesis.
Addocat 102 is a derivative of imidazole used in the production of pharmaceuticals, pesticides, ion exchange resins, dye intermediates, textile auxiliaries, photographic chemicals, and corrosion inhibitors.


Addocat 102 can also be used as a catalyst for the manufacture of polyurethane and a curing agent for epoxy resins.
For example, when Addocat 102 is added to an aqueous diethylenetriamine (DETA) solution, high CO2 loading can be achieved through phase separation of the absorbent during CO2 absorption.


Addocat 102 is also used as a catalyst for manufacturing polyurethanes and a curing agent for epoxy resins.
Addocat 102 is an aprotic solvent.


-Applications of Addocat 102:
*Continuous production of sandwich panels.
*Discontinuous heat/cold insulation of refrigerators and piping.
*On-site casting.



CHEMICAL PROPERTIES OF ADDOCAT 102:
Addocat 102 is an aromatic heterocyclic organic compound with the formula C4H6N2.
Addocat 102 is a colorless to yellow liquid, with an amine-like odor.
Addocat 102 is miscible with water.

Addocat 102 is an important raw material for the synthesis of pharmaceutical intermediates, used in the preparation of losartan, nizofenone, 1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride and naphazoline hydrochloride, etc.
Addocat 102 is also used as a specialty solvent, a base, and as a precursor to some ionic liquids.



PREPARATION OF ADDOCAT 102:
Addocat 102 is prepared mainly by two routes industrially.
The main one is acid-catalysed methylation of imidazole by methanol.

The second method involves the Radziszewski reaction from glyoxal, formaldehyde, and a mixture of ammonia and methylamine.
(CHO)2 + CH2O + CH3NH2 + NH3 → H2C2N(NCH3)CH + 3 H2O
Addocat 102 can be synthesized on a laboratory scale by methylation of imidazole at the pyridine-like nitrogen and subsequent deprotonation.

Similarly, Addocat 102 may be synthesized by first deprotonating imidazole to form a sodium salt followed by methylation.
H2C2N(NH)CH + CH3I → [H2C2(NH)(NCH3)CH]I
[H2C2(NH)(NCH3)CH]I + NaOH → H2C2N(NCH3)CH + H2O + NaI



FUNCTION OF ADDOCAT 102:
Catalyst for the production of rigid polyurethane foam.



DOSAGE OF ADDOCAT 102:
0.5 - 1.0 p.b.w. Addocat 102, calculated on 100 p.b.w. polyol, together with 1 - 3 p.b.w Addocat PP or Addocat 726 b or 0.3 - 1.0 p.b.w. Addocat 104.



STORAGE AND TRANSPORTATION OF ADDOCAT 102:
Addocat 102 should be sealed and stored in dry, cool and ventilated warehouse, filled with nitrogen and sealed in a cool and dry place for storage.



PURIFICATION METHODS OF ADDOCAT 102:
Dry Addocat 102 with sodium metal and then distil it.
Store Addocat 102 at 0o under dry argon.
The picrate has m 159.5-160.5o (from H2O).



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 102:
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical Composition: 1-methylimidazole
Physical Form: Liquid
Chemical Composition: Tertiary amine
Physical Form: Clear, colorless to pale yellow liquid
Density (20 °C): Approx. 1.03 g/cm³
Viscosity (25 °C): Approx. 2 mPa.s
Boiling Point: 198 °C
Solidification Point: Approx. -2 °C
Flash Point: 92 °C (ASTM-D 93, DIN EN 22719)
Miscibility with Water: Miscible

Water Content: Max. 0.5%
Substance Content: Min. 99.0%
Relative Density: 1.030
Refractive Index: 1.4970
Flash Point (℃): 92
Melting Point (°C): -60
Boiling Point (°C): 198
Appearance: Colorless transparent liquid
Content: ≥99%
Density: 1.03 g/mL at 25 ℃
Vapor Pressure: 0.4 mm Hg (20 ℃)
Color: Clear colorless to yellow

Specific Gravity: 1.031
pKa: 6.95 (at 25℃)
BRN: 105197
Storage Temp.: Store below +30°C
Refractive Index: n20/D 1.495 (lit.)
Form: Liquid
pH Range: 9.5 - 11.5 at 100 g/L at 20 °C
pH: 9.5-10.5 (50 g/L, H2O, 20℃)
InChIKey: MCTWTZJPVLRJOU-UHFFFAOYSA-N
Explosive Limit: 2.7-15.7% (V)
Fp: 198 °F
Vapor Pressure: 0.4 mm Hg (20 °C)
EPA Substance Registry System: 1H-Imidazole, 1-methyl- (616-47-7)
Density: 1.03 g/mL at 25 °C (lit.)
Water Solubility: Miscible with water

Melting Point: −60 °C (lit.)
Stability: Stable, but moisture sensitive.
Incompatible with acids, acid anhydrides, strong oxidizing agents,
moisture, carbon dioxide, acid chlorides.
Sensitive: Hygroscopic
NIST Chemistry Reference: 1H-Imidazole, 1-methyl- (616-47-7)
CAS DataBase Reference: 616-47-7 (CAS DataBase Reference)
Molecular Weight: 82.10 g/mol
XLogP3: -0.1
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 82.053098200 g/mol
Monoisotopic Mass: 82.053098200 g/mol
Topological Polar Surface Area: 17.8 Ų

Heavy Atom Count: 6
Formal Charge: 0
Complexity: 44.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Purity / Analysis Method: >99.0% (GC)
Molecular Formula: C4H6N2
Molecular Formula / Molecular Weight: C4H6N2 = 82.11
Physical State (20 °C): Liquid

Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas: Store under inert gas
Condition to Avoid: Air Sensitive, Hygroscopic
CAS RN: 616-47-7
Reaxys Registry Number: 105197
PubChem Substance ID: 87572549
SDBS (AIST Spectral DB): 3569
MDL Number: MFCD00005292
CB Number: CB1316726
MOL File: 616-47-7.mol
Melting Point: −60 °C (lit.)
Boiling Point: 198 °C (lit.)
Density: 1.03 g/mL at 25 °C (lit.)

Vapor Pressure: 0.4 mm Hg (20 °C)
Refractive Index: n20/D 1.495 (lit.)
Flash Point: 198 °F
Storage Temp.: Store below +30°C
Solubility: Chloroform (Slightly), Methanol (Slightly)
Form: Liquid
pKa: 6.95 (at 25°C)
Specific Gravity: 1.031
Color: Clear colorless to yellow
pH: 9.5-10.5 (50 g/L, H2O, 20°C)
pH Range: 9.5 - 11.5 at 100 g/L at 20 °C
Explosive Limit: 2.7-15.7% (V)

Water Solubility: Miscible with water
Sensitive: Hygroscopic
BRN: 105197
Stability: Stable, but moisture sensitive.
Incompatible with acids, acid anhydrides, strong oxidizing agents,
moisture, carbon dioxide, acid chlorides
InChIKey: MCTWTZJPVLRJOU-UHFFFAOYSA-N
LogP: -0.19 at 25°C
CAS DataBase Reference: 616-47-7
EWG's Food Scores: 1
FDA UNII: P4617QS63Y
NIST Chemistry Reference: 1H-Imidazole, 1-methyl- (616-47-7)
EPA Substance Registry System: 1H-Imidazole, 1-methyl- (616-47-7)



FIRST AID MEASURES of ADDOCAT 102:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 102:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 102:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 102:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 102:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 102:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 105
Addocat 105 is one of the standard catalysts for polyurethanes.
In foam production Addocat 105 activates both the gas reaction and the crosslinking reaction.


CAS Number: 280-57-9
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Solution of triethylene diamine in dipropylene glycol
Molecular formula: C6H12N2



SYNONYMS:
Addocat DB Addocat DMEA Addocat LTP Addocat PP Addocat PV Addocat SO Addocat 101 Addocat 102 Addocat 104 ADDOCAT 105 Addocat 106 Addocat 108 Addocat 10/9 Addocat 117 Addocat 1221 VN Addocat 1656 Addocat 1926 Addocat 201 Addocat 30EL08 Addocat 3144 Addocat 5073 Addocat 726 B Addocat 9018 Addocat 9558
Catalyst A33, Polyurethane Catalyst A33, Catalyst A33, Foaming Catalyst A33, CAS 280-57-9, Dabco 33-LV, Niax A-33, Jeffcat TD-33A, Lupragen N201, Tegoamin 33 PC CAT TD33, Addocat 105, TEDA L33, foaming catalyst, polyurethane foaming catalyst, catalyst A-33, polyurethane catalyst A-33, liquid catalyst, liquid complex amine catalyst, A33 Polyurethane Catalyst A33, Catalyst A33, Dabco 33-LV, Niax A-33, Jeffcat TD-33A, Lupragen N201, Tegoamin 33, PC CAT TD33, Addocat 105, TEDA L33, Foaming Catalyst A33, Addocat 10/9, Addocat 101, Addocat 102, Addocat 104, Addocat 105, Addocat 106, Addocat 108, Addocat 117, Addocat 1221 VN, Addocat 1656, Addocat 1926, Addocat 201, Addocat 30EL08, Addocat 3144, Addocat 5073, Addocat 726 B, Addocat 9018, Addocat 9558, Addocat DB, Addocat DMEA, Addocat LTP, Addocat PP, Addocat PV, Addocat SO



Addocat 105 is a gel catalyst mainly used as polyurethane foam.
Addocat 105 is form Solid
Addocat 105 is a general purpose catalyst used in polyurethane systems for the production of rigid, flexible polyurethane foams and microcellular foams.


Addocat 105 is a solution of triethylene diamine in dipropylene glycol.
Addocat 105 acts as a catalyst for the production of polyurethanes.
In foam production, Addocat 105 activates both the gas reaction and the crosslinking reaction.


Flexible polyether foam: In the production of polyether slabstock foam and hot-moulded foam, Addocat 105 serves mainly to promote the gas reaction.
Addocat 105 is suitable for flexible slabstock foam, hot moulded foam, HR foam, filling foam, integral skin foam, rigid foam and polyurethane coatings, elastomers and other products.


Addocat 105 has a shelf life of 12 months.
Addocat 105 is one of the standard catalysts for polyurethanes.
In foam production Addocat 105 activates both the gas reaction and the crosslinking reaction.


Addocat 105 is one of the standard catalysts for polyurethanes.
In foam production Addocat 105 activates both the gas reaction and the crosslinking reaction.
Addocat 105 is a polyurethane catalyst based on a tertiary amine, specifically triethylenediamine cut in DPG.
Addocat 105 is a balanced catalyst, activating both the gelling (cross linking) reaction and blowing reaction in polyurethane foams.



USES and APPLICATIONS of ADDOCAT 105:
Addocat 105 is solid at room temperature and is not suitable for use as a polyurethane catalyst.
In industrial applications, Addocat 105 is often dissolved into small molecule diols and configured for use as an alcoholic solution at 33% by weight (or other concentrations).


Commonly Addocat 105 is used diols are dipropylene glycol monoacetate, propylene glycol, diethylene glycol monoacetate (diethylene glycol), ethylene glycol, etc.
Addocat 105 is used flexible, semi-rigid, rigid urethane foam


Cold-curing cast elastomers use of Addocat 105: In the production of cold-curing cast elastomers Addocat 105
(0.1 - 0.5 p.b.w.) is used wherever relatively long filling times are desired.
Addocat 105 is suitable for use in flexible slabstock foam, hot moulded foam, HR foam, filling foam, integral skin foam, rigid foam.


Addocat 105 is also suitable for use in polyurethane coatings, elastomers, and sealants.
Addocat 105 is used continuous and discontinuous production of sandwich panels.
Addocat 105 is used discontinuous cold/heat insulation of refrigerators and piping.


Addocat 105 is used on-site casting.
HR-foam (moulded and slabstock foam) uses of Addocat 105: Here the reaction can be controlled with Addocat 105 (0.3 - 1.0 p.b.w. on 100 p.b.w. polyol) in combination with Addocat 108 (0.1 - 0.5 p.b.w.).


-Filling foam uses of Addocat 105:
In the production of semi-rigid filling foams Addocat 105 has been found advisable to use triethanol amine (up to 4.0 p.b.w.) in addition to Addocat 105 .
This improves the open cell structure.


-Rigid foam uses of Addocat 105:
Addocat 105 gives rigid foams a tough and elastic skin, thus
improving the adhesion of the foam to flexible and rigid facings.

Addocat 105 can be used alone, but also in combination with
Addocat 726 b and Addocat PP.
Dosage of Addocat 105: 1.0 - 3.0 p.b.w. on 100 p.b.w. polyol.


-Integral skin foam (flexible, semi-rigid, rigid) uses of Addocat 105:
In the production of integral skin foam Addocat 105 (1.0 - 2.0
p.b.w.) is used together with Addocat 201 (0.02 - 0.05 p.b.w.). Combinations of the two activators reduce the demoulding times.


-Flexible polyether foam uses of Addocat 105:
In the production of polyether slabstock foam and hot-moulded foam Addocat 105 serves mainly to promote the gas reaction (0.3 - 0.45 p.b.w. on 100 p.b.w. polyol).
Addocat 105 is used together with Addocat SO (0.1- 0.3 p.b.w.), which activates the crosslinking reaction.



USAGE OF ADDOCAT 105:
The active ingredient of polyurethane catalyst A33 is Addocat 105, the solution prepared by 33% of Addocat 105 and 67% of monoconjugated dipropylene glycol is mainly used as gel catalyst for polyurethane foam, which is widely used in flexible, semi-rigid, rigid polyurethane foam, coating, elastomer, In polyurethane foaming system, isocyanate firstly reacts with Addocat 105 to generate active complex.

The nature of the complex is very unstable, once the urethane bond is generated, it will be free, which is conducive to further catalyzing, Addocat 105 has a strong catalytic effect on the gel reaction and foaming reaction, especially on the polyurethane and hydroxyl catalytic effect is more selective.
Addocat 105 is mainly used as gel catalyst for polyurethane foams, and it is widely used in flexible, semi-rigid, rigid polyurethane foams, elastomers, coatings, etc.



CHEMICAL COMPOSITION OF ADDOCAT 105:
33% solution of Addocat 105.
Addocat 105 is solid at room temperature and is not convenient for use as a polyurethane catalyst.

In industrial applications, Addocat 105 is often melted in small molecule diols and configured to be used as an alcohol solution with a mass fraction of 33% (or other concentrations).
Commonly Addocat 105 is used diols are dipropylene glycol monoacetate, propylene glycol, diethylene glycol monoacetate (diethylene glycol), ethylene glycol and so on.



STORAGE STABILITY OF ADDOCAT 105:
When Addocat 105 is stored in firmly closed containers, a shelf life of 12 months can be expected.
Handling
Consult material safety data sheet (MSDS) for additional handling information for Addocat 105 .



FUNTION OF ADDOCAT 105:
Catalyst for the production of polyurethanes, e.g. flexible slabstock foam, hot molded foam, HR foam, filling foam, integral skin foam, rigid foam and polyurethane coatings, elastomers and other products.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 105:
Molecular formula: C6H12N2
Relative molecular mass: 112.17
CAS No.: 280-57-9
Purity ≥99%
Moisture ≤0.5%
Viscosity (25℃): 100mPa.s
Density (20℃): 1.033g/cm3
Flash point (PMCC): 79℃
Vapor pressure (38℃): 266Pa

Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Solution of triethylene diamine in dipropylene glycol
Physical Form: Liquid
Density (20 °C): 1.03 g/cm³
Viscosity (20 °C): Approx. 148 mPa.s
Initial Boiling Point: 198 °C
Pour Point: Approx. -33 °C
Flash Point: 92 °C (DIN EN 22719, ASTM-D 93)
OH-Value: Approx. 560 mg KOH/g
Miscibility with Water: Unlimited
Water Content: Max. 0.5 %
TEDA Content: 33.3 ± 0.5 %



FIRST AID MEASURES of ADDOCAT 105:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 105:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 105:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 105:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 105:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 105:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 106
Addocat 106 acts as a catalyst for polyurethane.
Addocat 106 is suitable for use in semi-rigid integral systems such as formulations for shoe soles, armrests for cars.


Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: 25% solution of triethylene diamine in 1,4 butanediol



SYNONYMS:
Dabco 33-S, Dabco 33S 33% BDO solution of triethylenediamine, Advocate 106, TEDA-L33B, DABCO POLYCAT micro-catalyst, small catalyst, Gel catalyst Dabco 33S, 25 % solution of triethylene diamine in 1,4 butanediol



Addocat 106 is 25 % solution of triethylene diamine in 1,4 butanediol.
Addocat 106 acts as a catalyst for polyurethane.


Addocat 106 is suitable for use in semi-rigid integral systems such as formulations for shoe soles, armrests for cars.
Addocat 106 has a shelf life of 12 months.



USES and APPLICATIONS of ADDOCAT 106:
Addocat 106 is specifically used for semi-rigid integral systems such as formulations for shoe soles, armrests for cars, etc. and for polyurethane coatings and elastomers manufactured by cold casting.


Approximately 1 - 2 p.b.w. Addocat 106 to 100 p.b.w. polyol blend are used, depending on the demold time required.
Demold time can be reduced even further by using organo-metallic compounds such as Addocat 201 (approx. 0.03 p.b.w.).
Addocat 106 is used catalyst for polyurethane Plastic- and Rubberpolymers Polymer auxiliaries


Addocat 106 is suitable for recipes which also contain 1,4 butanediol.
Addocat 106 acts as a catalyst for polyurethane.
Addocat 106 is suitable for use in semi-rigid integral systems such as formulations for shoe soles, armrests for cars.



FUNCTION OF ADDOCAT 106:
Catalyst for polyurethane.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 106:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: 25% solution of triethylene diamine in 1,4 butanediol
Physical Form: Liquid



FIRST AID MEASURES of ADDOCAT 106:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 106:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 106:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 106:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 106:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 106:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SEO keywords:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: 25% solution of triethylene diamine in 1,4 butanediol
Dabco 33-S; Dabco 33S 33% BDO solution of triethylenediamine; Advocate 106; TEDA-L33B; DABCO POLYCAT micro-catalyst; small catalyst; Gel catalyst Dabco 33S; 25 % solution of triethylene diamine in 1;4 butanediol
SEO description:
Addocat 106 is suitable for use in semi-rigid integral systems such as formulations for shoe soles, armrests for cars.













ADDOCAT 106


Addocat 106 poliüretan için katalizör görevi görür.
Addocat 106, ayakkabı tabanları, araba kolçakları gibi yarı sert integral sistemlerde kullanıma uygundur.


Ürün Tipi: Polimerizasyon Başlatıcılar / İnhibitörler / Katalizörler > Katalizörler
1,4 bütandiolde %25 trietilen diamin çözeltisi



EŞ ANLAMLI:
Dabco 33-S, Dabco 33S %33 BDO trietilendiamin çözeltisi, Advocate 106, TEDA-L33B, DABCO POLYCAT mikrokatalizör, küçük katalizör, Jel katalizör Dabco 33S, 1,4 bütandiol içinde %25 trietilen diamin çözeltisi



Addocat 106, 1,4 bütandiol içindeki %25 trietilen diamin çözeltisidir .
Addocat 106 poliüretan için katalizör görevi görür.


Addocat 106, ayakkabı tabanları, araba kolçakları gibi yarı sert integral sistemlerde kullanıma uygundur.
Addocat 106'nın raf ömrü 12 aydır.



ADDOCAT 106'NIN KULLANIMLARI ve UYGULAMALARI:
Addocat 106 özellikle ayakkabı tabanları, araba kolçakları vb. için formülasyonlar gibi yarı sert entegre sistemler ve soğuk dökümle üretilen poliüretan kaplamalar ve elastomerler için kullanılır.


Gerekli kalıptan çıkarma süresine bağlı olarak yaklaşık 1 - 2 pbw Addocat 106 ila 100 pbw poliol karışımı kullanılır.
Addocat 201 (yaklaşık 0,03 pbw) gibi organo-metalik bileşikler kullanılarak kalıptan çıkarma süresi daha da kısaltılabilir.
Addocat 106, poliüretan Plastik ve Kauçukpolimerler Polimer yardımcıları için katalizör olarak kullanılır.


1,4 bütandiol içeren tarifler için de uygundur .
Addocat 106 poliüretan için katalizör görevi görür.
Addocat 106, ayakkabı tabanları, araba kolçakları gibi yarı sert integral sistemlerde kullanıma uygundur.



ADDOCAT 106'NIN İŞLEVİ:
Poliüretan için katalizör.



ADDOCAT 106'NIN FİZİKSEL ve KİMYASAL ÖZELLİKLERİ:
Ürün Tipi: Polimerizasyon Başlatıcılar / İnhibitörler / Katalizörler > Katalizörler
1,4 bütandiolde %25 trietilen diamin çözeltisi
Fiziksel Form: Sıvı



ADDOCAT 106 İLK YARDIM ÖNLEMLERİ:
-İlk yardım önlemlerinin açıklaması
*Genel tavsiye:
Bu malzeme güvenlik bilgi formunu görevli doktora gösterin.
*Solunması halinde:
İnhalasyondan sonra:
Temiz hava aldırın.
*Ciltle teması halinde:
Kirlenmiş olan giysilerinizi hemen çıkarınız.
Cildi suyla durulayın
su / duş.
*Göz teması halinde:
Göz temasından sonra:
Bol su ile durulayın.
Göz doktorunu çağırın.
Kontakt lensleri çıkarın.
*Yutulması halinde:
Yuttuktan sonra:
Derhal kazazedeye su içirin (en fazla iki bardak).
Bir hekime danışın.
-Herhangi bir acil tıbbi müdahale ve özel tedavi ihtiyacının belirtilmesi.
Veri yok



ADDOCAT 106'NIN KAZA SONUCU YAYILMASINA KARŞI ÖNLEMLER:
-Çevresel önlemler:
Ürünün kanalizasyona girmesine izin vermeyin.
- Muhafaza etme ve temizlemeye yönelik yöntemler ve materyaller:
Drenajları kapatın.
Dökülenleri toplayın, bağlayın ve pompalayın.
Olası malzeme sınırlamalarına dikkat edin.
Kuru alın.
Uygun şekilde imha edin.
Etkilenen bölgeyi temizleyin.



ADDOCAT 106 YANGINLA MÜCADELE ÖNLEMLERİ:
-Yıkıcı medya:
*Uygun söndürücü maddeler:
Karbondioksit (CO2)
Köpük
Kuru toz
*Uygun olmayan söndürme maddeleri:
Bu madde/karışım için söndürücü maddelere ilişkin herhangi bir sınırlama verilmemiştir.
-Daha fazla bilgi:
Yangın söndürme suyunun yüzey suyuna veya yeraltı suyu sistemine karışmasını önleyin.



ADDOCAT 106'NIN MARUZ KALMA KONTROLLERİ/KİŞİSEL KORUNMASI:
-Kontrol parametreleri:
--İşyeri kontrol parametrelerine sahip malzemeler:
-Maruz kalma kontrolleri:
--Kişisel koruyucu ekipman:
*Göz/yüz koruması:
Göz koruması için ekipman kullanın.
Emniyet gözlükleri kullanın
*Vücut koruması:
koruyucu giysi giyin.
*Solunum koruma:
Önerilen Filtre tipi: Filtre A
-Çevresel maruziyetin kontrolü:
Ürünün kanalizasyona girmesine izin vermeyin.



ADDOCAT 106'NIN KULLANILMASI ve DEPOLANMASI:
-Herhangi bir uyumsuzluk da dahil olmak üzere güvenli depolama koşulları:
*Depolama koşulları:
Sıkıca kapalı tutun.
Kuru tutun.



ADDOCAT 106'NIN KARARLILIĞI ve REAKTİVİTESİ:
-Kimyasal stabilite:
Ürün, standart ortam koşulları (oda sıcaklığı ) altında kimyasal olarak stabildir.
-Tehlikeli reaksiyon olasılığı:
Veri yok


ADDOCAT 108
Addocat 108 is a clear, Colorless to yellowish.
Addocat 108 is a mixture of bis-(2-dimethyl-aminoethyl)-ether and dipropylene glycol.


CAS Number: 3033-62-3
Product Type: Polyurethane-Amine
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of bis-(2-dimethyl-aminoethyl)-ether and dipropylene glycol
Molecular formula: C8H20N2O



SYNONYMS:
Polyurethane Catalyst A-1, Catalyst A-1, Dabco BL-11, Niax A-1, Jeffcat ZF-22, Lupragen N206, Tegoamin BDE, PC CAT NP90, Addocat 108, Toyocat ET



Addocat 108 is a polyurethane catalyst based on a tertiary amine, specifically Bis-(2-diemthylaminoethyl)-ether cut in DPG.
Addocat 108 strongly activates the blowing reaction for flexible and rigid polyurethane foams.
In rigid foams, Addocat 108 improves the flow of the reaction mixture, normally used as a co-catalyst.


Addocat 108 is a clear, Colorless to yellowish.
Addocat 108 is a mixture of bis-(2-dimethyl-aminoethyl)-ether and dipropylene glycol.
Addocat 108 is suitable for continuous production of panels and slabstock - discontinuous heat/cold insulation of piping and refrigerators.


Addocat 108 has a shelf life of 12 months.
Addocat 108 is a mixture of bis-(2-dimethyl-aminoethyl)-ether and dipropylene glycol.
Addocat 108 acts as a activator for the production of polyurethane flexible slab-stock foam and hot-molded foam.


Addocat 108 has a shelf life of 12 months.
Addocat 108 is a powerful catalyst for the gas reaction.



USES and APPLICATIONS of ADDOCAT 108:
Addocat 108 is mainly used in the production of flexible polyether-type polyurethane foam, and can also be used in the production of rigid foam for packaging, especially suitable for the production of high resilience, semi-rigid foam and low density Foam;
Addocat 108 is used in conjunction with organotin catalysts to provide a significant increase in foam production tolerance.


Addocat 108 acts as a activator for the production of polyurethane flexible slab-stock foam and hot-molded foam.
Addocat 108 is used for HR foam and, as a co-catalyst, for rigid foams.
Addocat 108 is mainly used in the production of flexible polyether-type polyurethane foam, and can also be used in the production of rigid foam for packaging, especially suitable for the production of high resilience, semi-rigid foam and low density foam;


Addocat 108 is used in conjunction with organotin catalysts to provide a significant increase in foam production tolerance.
Addocat 108 is sued continuous production of panels and slabstock.
Addocat 108 is used discontinuous heat/cold insulation of piping and refrigerators.


HR foam (moulded and slabstock foam) uses of Addocat 108: In this case the reaction can be controlled with Addocat 108 (0.1 - 0.5 p.b.w. on 100 p.b.w. polyol) in combination with Addocat 105 (0.3 -1.0 p.b.w.).
Addocat 108 is also used for HR foam and, as a co-catalyst, for rigid foams.


Addocat 108 is suitable for continuous production of panels and slabstock.
Addocat 108 is used discontinuous heat/cold insulation of piping and refrigerators.


-Filling foam uses of Addocat 108:
In the production of semi-rigid filling foam Addocat 108 has been found advisable to use
triethanol amine (up to 4.0 p.b.w.) in addition to Addocat 108 .
This gives a more open cell structure.


-Rigid foam uses of Addocat 108:
In rigid foam systems Addocat 108 is used only as a co-catalyst in combination with Addocat 726 b, Addocat 1926, Addocat 1221 or Addocat 9412.
Even small additions of Addocat 108 (0.1 p.b.w.) improve the flowability of the system.


-Flexible polyether foam uses of Addocat 108:
Addocat 108 is one of the standard catalysts used to promote the gas reaction in the production of polyether slabstock foam and hot-moulded foam (dosage 0.1 - 0.15 p.b.w. on 100 p.b.w. polyol).
Here Addocat 108 is always used in combination with Addocat SO (0.1 - 0.3 p.b.w.).



STORAGE STABILITY OF ADDOCAT 108:
When Addocat 108 is stored in firmly closed original containers
a shelf life of 12 months can be expected.
Possible yellowing of the liquid in the course of time has no influence on the product's catalytic effect.



FUNCTION OF ADDOCAT 108:
Addocat 108 is used for the production of polyurethane flexible slabstock foam and hot-moulded foam.
Addocat 108 is also used for HR foam and, as a co-catalyst, for rigid foams.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 108:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of bis-(2-dimethyl-aminoethyl)-ether and dipropylene glycol
Physical Form: Liquid
Chemical composition: Active substance mixture of bis-(2-dimethyl-aminoethyl)- ether and dipropylene glycol
Physical form: clear, colourless to slightly yellowish liquid
Density (20 °C): approx. 0,90 g/cm³
Viscosity (25 °C): approx. 4 mPa.s
Initial boiling point: approx. 170 °C
Solidification point: approx. - 80 °C
Flash point: approx. 71 °C (DIN EN 22719, ASTM-D 93)

Miscibility with water: miscible
Water content: max. 0.5 % 70.0 ± 1.0 %
Molecular formula: C8H20N2O;
Relative molecular mass: 160.3;
CAS No.: 3033-62-3;
Light yellow transparent liquid;
Purity ≥99%;
Water content ≤0.5%;
Viscosity (25℃): 4.1mPa.s;
Density (25℃): 0.902g/cm3;
Flash point (PMCC): 74℃;
Vapor pressure (20℃): 1.3Pa;
Boiling range: 186-226°C;

Formula:C8H20N2O
InChI:InChI=1S/C8H20N2O/c1-9(2)5-7-11-8-6-10(3)4/h5-8H2,1-4H3
InChI key:InChIKey=GTEXIOINCJRBIO-UHFFFAOYSA-N
SMILES:O(CCN(C)C)CCN(C)C
Molecular formula: C8H20N2O
Relative molecular mass: 160.3
CAS number: 3033-62-3
Light yellow transparent liquid
Purity ≥99%
Moisture≤0.5%
Viscosity (25℃): 4.1mPa.s
Density (25℃): 0.902g/cm3
Flash point (PMCC): 74℃
Vapor pressure (20℃): 1.3Pa
Boiling range: 186-226℃



FIRST AID MEASURES of ADDOCAT 108:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 108:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 108:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 108:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 108:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 108:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

ADDOCAT 117
Addocat 117 is to 100 p.b.w. polyester polyol.
Addocat 117 is 1,4-dimethylpiperazine.


Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: 1,4-dimethylpiperazine



SYNONYMS:
Jeffcat DMP, Lupragen N204, PC CAT DMP, Addocat 117, Gel balance catalyst, Polyurethane foaming gel balance catalyst, 1,4-dimethylpiperazine, DMP, Lupragen N204, PC CAT DMP, Addocat 117, Gel Balance Catalyst, Polyurethane Foaming Gel Balance Catalyst, 1,4-Dimethylpiperazine



Addocat 117 is an excellent co-catalyst for all polyurethane systems.
Addocat 117 is 1,4-dimethylpiperazine.
Addocat 117 acts as a co-catalyst for polyurethanes, especially for low odour polyester flexible slabstock foam.


Dosage of Addocat 117 should be between 0.1 and 0.5 p.b.w.
Addocat 117 to 100 p.b.w. polyester polyol.
Addocat 117 has a shelf life of 12 months.


Addocat 117 is a colorless to light yellow liquid, soluble in water, and its aqueous solution is weakly alkaline.
Addocat 117 is an excellent co-catalyst for all polyurethane systems.
Addocat 117 is especially suited to be used as co-catalyst for the reduced odor catalysis of flexible polyester slabstock in combination with urea, Addocat DMEA and Addocat SO.


Addocat 117 is a polyurethane catalyst based on a tertiary amine based i=on N,N-dimethyl piperazine (DMP).
Addocat 117 activates the gelling (cross linking) reaction for flexible polyurethane foams.
Addocat 117 is particularly suitable as a co-catalyst for low odor polyester polyurethane flexible slabstock foam.


Addocat 117 is an excellent co-catalyst for all polyurethane systems.
Addocat 117 is especially suited to be used as co-catalyst for the reduced odour catalysis of flexible polyester slabstock in combination with urea, Addocat DMEA and Addocat SO.


Dosage of Addocat 117 should be between 0.1 and 0.5 p.b.w.
Addocat 117 to 100 p.b.w. polyester polyol.



USES and APPLICATIONS of ADDOCAT 117:
Addocat 117 can be used as a foaming/gelling balanced catalyst for polyurethane.
Addocat 117 can be used in polyurethane soft foam, polyurethane rigid foam, coatings, adhesives, etc.
Addocat 117 is beneficial to foam cell opening.


Addocat 117 can also be used in other intermediates such as pharmaceutical intermediates.
Addocat 117 is used polymer auxiliaries.
Addocat 117 is used ester foams.


Addocat 117 can also be used as pharmaceutical intermediates and other intermediates.
Addocat 117 is especially suited to be used as co-catalyst for the reduced odor catalysis of flexible polyester slabstock in combination with urea, Addocat DMEA and Addocat SO.



PHYSICAL AND CHEMICAL PROPERTIES OF ADDOCAT 117:
Addocat 117 is a colorless to light yellow liquid, soluble in water, and its aqueous solution is weakly alkaline.



FUNCTION OF ADDOCAT 117:
Co-catalyst for polyurethanes, specially for low odor polyester flexible slabstock foam.



STORAGE STABILITY OF ADDOCAT 117:
When Addocat 117 is stored in firmly closed original containers at about 20 °C, a shelf life of 6 months can be ex pected.
Prolonged exposure to temperatures above 30 °C may discolour the product, even in closed containers.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 117:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: 1,4-dimethylpiperazine
Physical Form: Liquid
Appearance: Colorless to yellowish liquid
Density at 20 °C: Approx. 0.85 g/cm³
Initial Boiling Point: 130-133 °C
Solidification Point: Approx. -1 °C
Flash Point (TCC): 22 °C
Viscosity at 25 °C: Approx. 1 mPa.s
Miscibility with Water: Unlimited
Water Content: Max. 0.5 %
Substance Content: Min. 98.0 %



FIRST AID MEASURES of ADDOCAT 117:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 117:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 117:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 117:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 117:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 117:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 118
Addocat 118 is suitable for the production of rigid polyurethane foams, especially for 1K and 2K cartridge systems.
Addocat 118 is an amine based catalyst that is also known as dimorpholino-diethyl ether.


CAS Number: 6425-39-4
EC Number: 229-194-7
Product Type: Polyurethane-Amine
Molecular formula: C12H24N2O3



SYNONYMS:
DMDEE, Bis(2,2-morpholinodiethyl)ether, CAS 6425-39-4, Catalyst DMDEE, Polyurethane Catalyst DMDEE, Foaming Catalyst DMDEE DMDEE, Dabco DMDEE, Jeffcat DMDEE, Lupragen DMDEE, Fodocatat DMDEE, PC Addocam N106, 118 Catalyst DMDEE, polyurethane foaming catalyst DMDEE, Nsc 28749, dimorpholine, Lupragen N106, Einecs 229-194-7, LUPRAGEN(R) N 106, 2,2-Dimorpholinodiet, Lupragen N106 (DMDEE), Dimorpholinodiethylether, Bis(morpholinoethyl)ether, Di(morpholinylethyl) ether



Addocat 118 is an amine based catalyst that is also known as dimorpholino-diethyl ether.
Addocat 118 can act as a catalyst for blowing reactions and facilitates the process of polymeric curing.
Addocat 118 is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.


Addocat 118 is a polyurethane catalyst based on a tertiary amine based on 2,2-dimorpholinyl-diethylether.
Addocat 118 is suitable for the production of rigid polyurethane foams, especially for 1K and 2K cartridge systems.


Addocat 118 improves storage conditions in these formulations.
While Addocat 118 is a good product, it is TRiiSO's opinion that we can supply much better options from Tosoh.



USES and APPLICATIONS of ADDOCAT 118:
Addocat 118 is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Addocat 118 is used in the following products: adhesives and sealants, coating products and polymers.


Other release to the environment of Addocat 118 is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Release to the environment of Addocat 118 can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).


Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Release to the environment of Addocat 118 can occur from industrial use: formulation of mixtures and formulation in materials.
Addocat 118 is used in the following areas: formulation of mixtures and/or re-packaging and building & construction work.
Addocat 118 is used for the manufacture of: furniture.


Release to the environment of Addocat 118 can occur from industrial use: in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates), in processing aids at industrial sites and as processing aid.
Release to the environment of Addocat 118 can occur from industrial use: manufacturing of the substance.


Addocat 118 is used catalyst for flexible polyester foams, molded foams, and moisture-cured foams and coatings.
Addocat 118 is used good blowing catalyst that does not cause cross-linking.
Use of the Substance/Mixture of Addocat 118: Additives for use in the production of polyurethanes


Addocat 118 is suitable for water curing system, it is a strong foaming catalyst, because the resistance effect of amino group in place can extend the storage time of NCO component, suitable for NCO catalytic reaction and water in TDI, MDI, IPDI and other systems.
Addocat 118 is mainly used in one-component rigid polyurethane foam system.


Addocat 118 can also be used in polyether-type and polyester-type polyurethane soft foam.
Addocat 118 can also be used in polyether-type and polyester-type foam type polyurethane soft foam, semi-hard foam, CASE materials, etc.
The added amount of Addocat 118 is 0.3-0.55% of the polyether/ester component.


Addocat 118 is an amine catalyst suitable for preservation systems.
Addocat 118 is primarily used in one-component rigid polyurethane foam systems, but can also be used in polyether-type and polyester-type polyurethane flexible foams, semi-rigid foams and CASE materials.


Addocat 118 is used as a catalyst (or hardener) in one-component polyurethane systems (eg, one-component polyurethane sealant, one-component polyurethane foam adhesive, one-component polyurethane jointing material, etc.).
Since single-component polyurethane prepolymers require long-term storage stability, Addocat 118 plays a key role in the stabilization and polymerization of polyurethane prepolymers, which also places very high demands on the quality of Addocat 118 products.


Addocat 118 is used as a catalyst (or hardener) in one-component polyurethane systems (e.g. one-component polyurethane caulk, one-component polyurethane foam adhesives, one-component polyurethane grouting materials, etc.).
Because one-component polyurethane prepolymers require long-term storage stability, Addocat 118 plays a key role in the stabilization and polymerization of polyurethane prepolymers, which also places very high demands on the quality of bismorpholine diethyl ether products.


Addocat 118 is suitable for water drying system, it is a strong foam catalyst, due to the resistance effect of the amino group site.
Addocat 118 can extend the storage period of the NCO component, suitable for the catalytic reaction of the NCO and water in TDI, MDI, IPDI and other systems.


Addocat 118 is mainly used in one-component rigid polyurethane foam system.
Addocat 118 can also be used in polyether and polyester type soft polyurethane foam.
Addocat 118 can also be used in polyether and polyester-type polyurethane soft foam , semi-rigid foam, CASE materials, etc.


The added amount of Addocat 118 is 0.3-0.55% of the polyether/ester component.
Addocat 118 is a suitable amine catalyst for curing systems.
Addocat 118 is a strong foam catalyst, which can make NCO-containing components have a long shelf life due to the blocking effect of the amine site.


Addocat 118 is primarily used in rigid one-component polyurethane foam systems, but can also be used in flexible polyether and polyester type polyurethane foams, semi-rigid foams and CASE materials.
Addocat 118 is a strong foaming catalyst that can make the NCO-containing component have a long shelf life due to the site-blocking effect of the amine.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 118:
Molecular formula: C12H24N2O3
Relative molecular mass: 244.0
CAS No.: 6425-39-4
Physical and chemical properties:
Bimorpholinodiethyl ether Appearance Colorless to light yellow liquid,
soluble in water.
Typical indices of physical property are:
Viscosity (25℃): 18mPa-s.
Relative density (25℃): 1.06;
Boiling point: greater than 225°C;
Melting point: less than -28°C;

Flash point (TCC): 146°C;
Amine value: 7.9-8.1 mmol/g.
CBNumber:CB9307993
Molecular Formula:C12H24N2O3
Molecular Weight:244.33
MDL Number:MFCD00072740
MOL File:6425-39-4.mol
Physical State: Liquid
Storage: Store at room temperature
Melting Point: -28 °C
Boiling Point: 192 °C at 2 kPa
Density: 1.06 g/mL at 25 °C (lit.)

Vapor Pressure: 66 Pa at 20 °C
Refractive Index: n20/D 1.484 (lit.)
Flash Point: 295 °F
Storage Temperature: 2-8 °C
Solubility: Slightly soluble in Chloroform and Ethyl Acetate
Form: Oil
pKa: 6.92 ± 0.10 (Predicted)
Color: Pale Brown to Light Brown
Viscosity: 216.6 mm²/s
Water Solubility: 100 g/L at 20 °C
InChIKey: ZMSQJSMSLXVTKN-UHFFFAOYSA-N
LogP: 0.5 at 25 °C
CAS DataBase Reference: 6425-39-4
FDA UNII: 5BH27U8GG4
EPA Substance Registry System: Morpholine, 4,4'-(oxydi-2,1-ethanediyl)bis- (6425-39-4)



FIRST AID MEASURES of ADDOCAT 118:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 118:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 118:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 118:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 118:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 118:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

ADDOCAT 1221 VN
Addocat 1221 VN turns yellow to brown on exposure to air and light, but without losing its catalytic effect.
Addocat 1221 VN allows a good start time and good cure.


Product Type: Polymerization Initiators / Inhibitors / Catalysts
Chemical Composition: Blend of tertiary amines with polyetherpolyol



Addocat 1221 VN is a blend of tertiary amines with polyetherpolyol.
Addocat 1221 VN acts as a catalyst for the manufacture of rigid polyurethane foams and building boards.
Addocat 1221 VN is hygroscopic and should therefore be protected from humidity.


Addocat 1221 VN should be stored in closed containers at temperatures of about 20°C.
Addocat 1221 VN turns yellow to brown on exposure to air and light, but without losing its catalytic effect.
Addocat 1221 VN allows a good start time and good cure.


For PUR rigid foam the dosage is approx. 2.0 - 4.0 p.b.w.
Addocat 1221 VN has a shelf life of 6 months.



USES and APPLICATIONS of ADDOCAT 1221 VN:
Addocat 1221 VN is used catalyst for the manufacture of rigid polyurethane foams
Addocat 1221 VN is hygroscopic and should therefore be protected from humidity.



FUNCTION OF ADDOCAT 1221 VN:
Addocat 1221 VN is mainly used for the continuous production of rigid slabstock foams and building boards.
Addocat 1221 VN allows a good start time and good cure.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 1221 VN:
Product Type: Polymerization Initiators / Inhibitors / Catalysts
Chemical Composition: Blend of tertiary amines with polyetherpolyol
Physical Form: Liquid



FIRST AID MEASURES of ADDOCAT 1221 VN:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 1221 VN:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 1221 VN:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 1221 VN:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 1221 VN:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 1221 VN:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 1926
Addocat 1926 acts as a catalyst for the production of rigid polyurethane foams.


Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of a tertiary amine and a polyol



SYNONYMS:
ADDOCAT 1926, Desmorapid trial product PU 1926, Tertiary amine in polyether polyol



Addocat 1926 is a mixture of a tertiary amine and a polyol.
Addocat 1926 acts as a catalyst for the production of rigid polyurethane foams.


Addocat 1926 is hygroscopic and should therefore be protected from air humidity.
As Addocat 1926 contains only 50 % of active ingredient, it must be used at dosages of 2 - 6 p.b.w., calculated on 100 p.b.w. polyether polyol.



USES and APPLICATIONS of ADDOCAT 1926:
Addocat 1926 is used continuous and discontinuous production of foam sheets and sandwich panels.
Addocat 1926 is used dscontinuous heat/cold insulation of piping and refrigeration equipment.


Addocat 1926 is used on-site casting.
Applications of Addocat 1926 include discontinuous production of foam sheets and sandwich panels, discontinuous heat/cold insulation of piping and refrigeration equipment, on-site casting.


Addocat 1926 has a shelf life of minimum six months.
Addocat 1926 is used Polymer auxiliaries, Housing for Electric and Electronics, In-situ foams, Construction material, Slabstock, Pipe insulation, and Body for electrical equipment.


Addocat 1926 catalyses the gas formation and crosslinking reactions and is used exclusively for rigid polyurethane foam systems.
As the product contains only 50% of active ingredient, Addocat 1926 must be used at dosages of 2 - 6 p.b.w. , calculated on 100 p.b.w. polyether polyol.
Addocat 1926 is particularly suitable for simple, yet accurate metering units as well as for automatic metering.



FUNCTION OF ADDOCAT 1926:
Catalyst for the production of rigid polyurethane foams.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 1926:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of a tertiary amine and a polyol
Physical Form: Liquid



FIRST AID MEASURES of ADDOCAT 1926:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 1926:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 1926:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 1926:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 1926:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 1926:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 201
Addocat 201 is a polyurethane catalyst based on an organometal compound, specifically Dibutyltin dilaurate (DBTDL).
Addocat 201 strongly activates the gelling (crosslinking) reaction in rigid polyurethane foams, elastomers and coatings.


CAS Number: 77-58-7
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Dibutyl tin dilaurate
Molecular Formula: (C4H9)2Sn(OOCC11H23)2



SYNONYMS:
Dibutyltin dilaurate, DBDLO, Dibutyltin dilaurate, Dibutyltin laurat, DBTL, MCT12, dibutyltin dilaurate , polyurethane catalyst T-12, organotin catalyst T12, organotin -T12 , catalyst T-12, Dabco T-12, Niax D-22, Kosmos 19, PC CAT T-12, Addocat 201 , organotin T-12 , dibutyltin dilaurate, organotin stabilizer, Foreign name: T-12



Addocat 201 catalyses the crosslinking reaction strongly.
Addocat 201 is a yellow liquid whose main ingredient is Dibutyl Tin Dilaurate, used as a catalyst for the production of polyurethanes such as PU paint, hard foams, soft foams, insulating foam sheets, elastic foam.


Addocat 201 is dibutyl tin dilaurate.
Addocat 201 acts as a catalyst for the production of polyurethanes, e.g. integral skin foams, rigid spray foam, cold-curing cast elastomers etc.
Addocat 201 considerably reduces the cure time.


Addocat 201 has a shelf life of 12 months.
Addocat 201 meets US Food and Drug Administration requirements for use in certain siloxanes.
Addocat 201 is a polyurethane catalyst based on an organometal compound, specifically Dibutyltin dilaurate (DBTDL).
Addocat 201 strongly activates the gelling (crosslinking) reaction in rigid polyurethane foams, elastomers and coatings.



USES and APPLICATIONS of ADDOCAT 201:
Addocat 201 is used additives for use in the production of polyurethanes
Addocat 201 is a catalyst intended for various applications.
Addocat 201 considerably reduces the cure time.


Addocat 201 can be used either individually or in combination with standard amine co-catalysts.
Addocat 201 is used in polyurethane systems (one- and two-component adhesive systems and sealants, in PU elastomers), in the production of silicone and silane-based sealants, as well as polyolefin-modified silane-based sealants.


Addocat 201 catalyses the crosslinking reaction strongly.
Integral skin foam (flexible and semi-rigid): In the production of integral skin foam Addocat 201 is used at 0.02 - 0.1 p.b.w. in addition to tertiary amines, such as Addocat 105 , of which the proportion used is 1.0 - 2.0 p.b.w. on 100 p.b.w. polyol.


-Rigid spray foam uses of Addocat 201:
Addocat 201 is used at 0.2 - 0.4 p.b.w. on 100 p.b.w. polyol
together with 0.5 - 2.0 p.b.w. tertiary amine, e.g.
Addocat 726 b and/or triethylamine, to accelerate the cure of rigid spray foam systems.


-Cold-curing cast elastomers uses of Addocat 201:
Addocat 201 is a highly effective catalyst for cold-curing cast
elastomers.
Even small additions (0.02 - 0.1 p.b.w. on 100 p.b.w. polyol)
greatly reduce the cure time (demoulding time).



FUNCTION OF ADDOCAT 201:
Catalyst for the production of polyurethanes, e.g. integral skin foams, rigid spray foam, cold-curing cast elastomers etc.



CHARACTERISTICS OF ADDOCAT 201:
When using Addocat 201, the curing speed will occur faster and the cross-linking reaction will be stronger.

*hard foam and soft foam (Integral skin foam)
For this type of foam, Addocat 201 is used at a rate of 0.02 - 0.1 percent by weight for polyols, in addition, people also use quaternary amines such as Addocat 105 at a rate of 1.0 - 2.0 percent.
Addocat 201 has the effect of reducing curing time.


*Insulation foam panels (Spray foam)
For this type of foam, the ratio of Addocat 201 used is 0.2 - 0.4 percent by weight for polyol along with 0.5 - 2% quaternary amine such as Addocat 726 b and (or) triethylamine to increase curing ability of this spray foam system.


*Elastic molded foam system
Addocat 201 is very effective for elastic molding foam systems.
Just a small amount of 0.02 - 0.1 percent by weight of polyol can significantly reduce curing time.

Addocat 201 is a polyurethane catalyst based on an organometal compound, specifically Dibutyltin dilaurate (DBTDL).
Addocat 201 strongly activates the gelling (crosslinking) reaction in rigid polyurethane foams, elastomers and coatings.



KEY FEATURES OF ADDOCAT 201:
Addocat 201 is one of the standard catalysts for PUR applications, e. g. integral skin foams, rigid spray foam,
cold-curing cast elastomers etc.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 201:
Chemical composition: dibutyl tin dilaurate
Physical form: clear yellow liquid
Density (20 °C): approx. 1.05 g/cm³
Viscosity (20 °C): approx. 50 mPa.s
Pour point: < 0 °C
Flash point: 149 °C (ASTM-D 93, DIN EN 22719)
Miscibility with water: not miscible, hydrolyses
Tin content: min. 18.3 %
Refractive index: 1.4700 ± 0.0100

Appearance: Pale yellow liquid
Freezing point: 10-15°C
Flash point: 232°C
Density (20°C): 1.03 – 1.06 g/cm³
Tin content: ≥ 17.5%
Color (Gardner): ≤ 3
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Dibutyl tin dilaurate
Physical Form: Liquid

Ingredient: Dibutyl Tin Dilaurate
External inspection: Clear yellow liquid
Density: ~ 1.05 g/cm³
Viscosity (20°C): ~ 50 mPa·s
Pouring temperature: < 0°C
Flash point: 149°C
Solubility in water: Does not dissolve
Tin content: Min 18.3%
Refractive index: 1.4700 ± 0.0100



FIRST AID MEASURES of ADDOCAT 201:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 201:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 201:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 201:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 201:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 201:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT 726 B
Addocat 726 B is a polyurethane catalyst based on a tertiary amine, specifically dimethylcyclohexylamine.
Addocat 726 B is a colorless liquid with a musky ammonia odor.


CAS Number: 98-94-3
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Dimethylcyclohexylamine
Molecular Formula: C8H17N



SYNONYMS:
N,N-DIMETHYLCYCLOHEXYLAMINE, 98-94-2, N,N-Dimethylcyclohexanamine, Cyclohexyldimethylamine, Dimethylcyclohexylamine, N-Cyclohexyldimethylamine, Cyclohexanamine, N,N-dimethyl-, (Dimethylamino)cyclohexane, Dimethylaminocyclohexane, Cyclohexylamine, N,N-dimethyl-, N,N-Dimethylaminocyclohexane, N,N-Dimethyl-N-cyclohexylamine, NSC 163904, Dimethylcyclicsiloxane hydrolyzate, N,N-dimethyl-cyclohexylamine, N1H19E7HTA, DTXSID9026633, CHEBI:59022, MFCD00003844, NSC-163904, HSDB 5323, EINECS 202-715-5, UN2264, UNII-N1H19E7HTA, BRN 1919922, N, N-Dimethylcyclohexylamine, 8IA, cyclohexyl-dimethylamine, dimethyl cyclohexylamine, dimethyl cyclohexyl amin, cyclohexane, dimethylamino-, Cyclohexanamine, N-dimethyl-, cyclohexyl(dimethyl)ammonium, Cyclohexylamine, N-dimethyl-, EC 202-715-5, N,N-dimethylcyclohexyl amine, SCHEMBL15595, N-cyclohexyl-N,N-dimethylamine, DTXCID906633, CHEMBL3186662, WLN: L6TJ AN1 & 1, N,N-Dimethylcyclohexylamine, 99%, STR02891, Tox21_201360, NSC163904, AKOS015850797, UN 2264, CAS-98-94-2, NCGC00249031-01, NCGC00258912-01, N,N-DIMETHYLCYCLOHEXYLAMINE [HSDB], DB-002820, D0705, NS00008221, Dimethylcyclohexylamine [UN2264], A845928, W-100060, Q25945666, F0001-2323, DMCHA, Dimethylcyclohexylamine, PC8, N,N-Dimethylcyclohexanamine, Polycat 8, DIMETHYLAMINOCYCLOHEXANE, N,N-Dimethylaminocyclohexane, Cyclohexanamine,N,N-dimethyl-, KL3, NiaxC8, Dimethylcyclohexylamine, DMCHA, N,N-dimethylcyclohexylamine, CAS: 98-94-2, Polycat 8, Niax C-8, Catalyst PC8, Catalyst PC-8, Polyurethane Catalyst PC-8, Rigid Foam Catalyst PC-8, cyclohexyldimethylamine, DMCHA, N,N-Dimethylcyclohexylamine, Dimethylcyclohexylamine, N,N-Dimethyl Cyclohexylamine



Addocat 726 B is a moderately active amine catalyst with low viscosity and can be used in a wide range of hard foams.
Addocat 726 B is dimethylcyclohexylamine.
Addocat 726 B acts as a catalyst for the production of rigid polyurethane foam.


Dosage: 1-3 p.b.w., calculated on 100 p.b.w. polyol.
Addocat 726 B has a shelf life of 12 months.
Addocat 726 B is a polyurethane catalyst based on a tertiary amine, specifically dimethylcyclohexylamine.


Addocat 726 B is a balanced gelling (cross linking) and blowing catalyst used in rigid polyurethane foams.
Addocat 726 B catalyzes the gas and crosslinking reaction of rigid polyurethane systems.
Addocat 726 B is hygroscopic and must therefore be protected from atmospheric humidity.


Addocat 726 B turns yellow on exposure to air and light, but without losing its catalytic effect.
Addocat 726 B should be stored at temperatures of about 20 °C.
Prolonged exposure to temperatures above 30 °C may cause discoloration, even in closed containers.


The storage life of Addocat 726 B in firmly closed original containers is 12 months.
Addocat 726 B is a colorless liquid with a musky ammonia odor.
Addocat 726 B is less dense than water.


Addocat 726 B is a tertiary amine consisting of cyclohexane having a dimethylamino substituent.
Addocat 726 B is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.


Addocat 726 B is low viscosity Amine catalyst.
Addocat 726 B is a tertiary amine consisting of cyclohexane having a dimethylamino substituent.
Addocat 726 B is a colorless liquid with a musky ammonia odor.


Addocat 726 B is water soluble.
Addocat 726 B is a low viscosity, moderately active amine catalyst for use in a wide range of rigid foams.
One of the main applications of Addocat 726 B is in formulations for insulation foams, spraying, panels, laminates, in-situ infusion and refrigeration, etc.


Addocat 726 B is also suitable for the manufacture of rigid foam furniture frames and decorative components.
Addocat 726 B Is a low viscosity of the secondary amine catalyst activity and rigid used in refrigerator, plank, spraying, the perfusion polyurethane hard foam at the scene.



USES and APPLICATIONS of ADDOCAT 726 B:
One of the main applications of Addocat 726 B is insulation foam, coating, plate, laminate, field pouring and refrigeration formulations.
Addocat 726 B is also suitable for the manufacture of rigid foam furniture frames and decorative parts.
Addocat 726 B is used insulation of refrigerators and foam filling of intricately shaped cavities.


Addocat 726 B is used continuous and discontinuous production of building board (foam thickness < 80 mm; also with rigid or metal facings) and of insulating panels with flexible facings (foam thickness 15-100 mm).
Addocat 726 B is used production of insulations by the layer-by-layer method.


Addocat 726 B is suitable for use in insulation of refrigerators and foam filling of intricately shaped cavities, continuous and discontinuous production of building board (foam thick-ness

Addocat 726 B is used catalyst for the production of rigid polyurethane foam
Addocat 726 B is used in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Release to the environment of Addocat 726 B can occur from industrial use: of articles where the substances are not intended to be released and where the conditions of use do not promote release.


Other release to the environment of Addocat 726 B is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Addocat 726 B can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones).
Addocat 726 B is used in the following products: polymers and adhesives and sealants.
Addocat 726 B is used in the following areas: formulation of mixtures and/or re-packaging, mining and building & construction work.


Addocat 726 B is used for the manufacture of: plastic products, machinery and vehicles and .
Release to the environment of Addocat 726 B can occur from industrial use: formulation in materials and in the production of articles.


Other release to the environment of Addocat 726 B is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Addocat 726 B is used in the following products: polymers.
Release to the environment of this substance can occur from industrial use: formulation in materials, in the production of articles and formulation of mixtures.


Other release to the environment of Addocat 726 B is likely to occur from: indoor use, outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Addocat 726 B is used in the following products: polymers and adhesives and sealants.
Addocat 726 B is used in the following areas: mining and building & construction work.
Addocat 726 B is used for the manufacture of: plastic products, machinery and vehicles and furniture.


Release to the environment of Addocat 726 B can occur from industrial use: in the production of articles, formulation in materials and in processing aids at industrial sites.
Addocat 726 B is specially used in the two components system, soluble with many kinds of rigid polyol and additive.


Other release to the environment of Addocat 726 B is likely to occur from: outdoor use, indoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Release to the environment of Addocat 726 B can occur from industrial use: manufacturing of the substance.
Addocat 726 B acts as a widely used catalyst.
Applications of Addocat 726 B include all types of rigid packaging foam.


Addocat 726 B is specially used in the two components system, soluble with many kinds of rigid polyol and additive.
Addocat 726 B is stable, compatible in the blend polyols.
Addocat 726 B is stable, compatible in the blend polyols.


Addocat 726 B is used for refrigerator,freezer,continuous panel,discontinuous panel,block foam,pour foam etc.
Addocat 726 B has been used as switchable hydrophilicity solvent (SHS) for the extraction of lipids from freeze-dried samples of Botryococcus braunii microalgae for biofuel production


Addocat 726 B on the gel and foam has a catalytic role, the rigid foam and gel reaction provides a balanced catalytic properties, properties of water and the reaction of isocyanate (foam) catalytic stronger, at the same time of polyols and isocyanates are moderate catalytic reaction, he is a strong initial catalyst foam reaction.


Addocat 726 B is used as catalyst in three-component organocatalyzed Strecker reaction on water
Except for hard bubble, Addocat 726 B can also be used for molding the soft, half hard bubble auxiliary catalysts, etc.
Addocat 726 B is used in polyurethane plastics and textiles and as a chemical intermediate.


-The curing temperature of baking finishes comprising polyurethane-forming substances can be reduced by 50 – 80 ℃ by adding weakly acidic derivatives of N,N-Dimethylcyclohexylamine.

Like pyridine, Addocat 726 B catalyzes certain reactions and is slightly more efficient than pyridine in the preparation of acid chlorides with thionyl chloride.
Addocat 726 B can be used as corrosion inhibitor and as an antioxidant in fuel oils.


-Industrial uses:
Addocat 726 B is used as a catalyst in the production of polyurethane foams.
Addocat 726 B is also used as an intermediate for rubber accelerators and dyes and in the treatment of textiles.



PROPERTIES AND USAGE OF ADDOCAT 726 B:
Addocat 726 B main purpose is as a catalyst for rigid polyurethane foams.
Addocat 726 B is a low-viscosity and medium-active amine catalyst used for refrigerators, plates, spraying, and on-site infusion of rigid polyurethane foams.

Addocat 726 B has a catalytic effect on gelation and foaming, and provides a more balanced catalytic performance for the foaming reaction and gelation reaction of rigid foam.
Addocat 726 B has a stronger catalyst for the reaction of water and isocyanate (foaming reaction), and at the same time.

The reaction of polyol feather isocyanate also has moderate catalysis.
Addocat 726 B is a strong initial catalyst for foam reaction.
In addition to hard foam, Addocat 726 B can also be used as an auxiliary foaming agent for molding soft foam and semi-rigid foam.
Addocat 726 B has stable performance in combined materials, great adjustability, and long-term storage.



PRODUCTTION METHODS OF ADDOCAT 726 B:
Addocat 726 B is manufactured either by the reaction of methyl chloride or formaldehyde and hydrogen with cyclohexylamine



FUNCTION OF ADDOCAT 726 B:
Addocat 726 B catalyses the gas and crosslinking reaction of rigid polyurethane systems.



CHEMICAL PROPERTIES OF ADDOCAT 726 B:
Addocat 726 B catalyst is a strongly basic, colorless liquid tertiary amine.
Addocat 726 B has a strong ammonia smell, placed for a long time the color will gradually become darker, but will not affect its chemical activity.
Addocat 726 B is soluble in most polyols and organic solvents, but insoluble in water.



REACTIVITY PROFILE OF ADDOCAT 726 B:
Addocat 726 B neutralizes acids in exothermic reactions to form salts plus water.
Addocat 726 B may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 726 B:
Chemical composition: dimethylcyclohexylamine
Physical form: clear, colourless to pale yellow liquid
Density (20 °C): approx. 0.85 g/ml
Viscosity (25 °C): approx. 2 mPa.s
Boiling range: 162 - 165 °C
Freezing point: approx. - 60 °C
Flash point: 41 °C (DIN 51755)
Miscibility with water: partially miscible
Water content: max. 0.25 %
Substance content: min. 99.0 %
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Dimethylcyclohexylamine
Physical Form: Liquid

Chemical Composition: Dimethylcyclohexylamine
Appearance: Colorless to light yellow transparent liquid
Density at 25 °C: 0.849 g/mL
Boiling point: 158-159 °C (lit.)
Melting point: -60 °C
Flash point: 108 °F
Refractive index: n20/D 1.454 (lit.)
Viscosity: 1.49 mm2/s
Water Solubility: 10 g/L at 20 °C
Vapor pressure: 3.6 mm Hg at 20 °C
Storage temperature: Store below +30 °C
PH: 12 (5g/l, H2O, 20 °C)
Explosive limit: 3.6-19% (V)
Freezing point: Sensitive: Air Sensitive

BRN: 1919922
Dielectric constant: 2.86
InChIKey: SVYKKECYCPFKGB-UHFFFAOYSA-N
LogP: 2.31 at 25 °C
Assay: 95.00 to 100.00%
Food Chemicals Codex Listed: No
Specific Gravity: 0.84900 @ 25.00 °C
Solubility: Water, 1.026e+004 mg/L @ 25 °C (est)
FDA UNII: N1H19E7HTA
NIST Chemistry Reference: Cyclohexanamine, N,N-dimethyl- (98-94-2)
EPA Substance Registry System: N,N-Dimethylcyclohexylamine (98-94-2)
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Dimethylcyclohexylamine
Physical Form: Liquid

Chemical Properties:
Molecular Formula: C8H17N
Molecular Weight: 127.23 g/mol
Exact Mass: 127.136099547 g/mol
Monoisotopic Mass: 127.136099547 g/mol
XLogP3: 1.9
Topological Polar Surface Area: 3.2 Ų
Heavy Atom Count: 9
Formal Charge: 0
Complexity: 72.6
Hydrogen Bond Donor Count: 0

Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 1
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Identifiers:
CAS Number: 98-94-2
MDL Number: MFCD00003844
CBNumber: CB1854754

Physical Properties:
Appearance: Colorless to light yellow transparent liquid
Density: 0.849 g/mL at 25 °C (lit.)
Boiling Point: 158-159 °C (lit.)
Melting Point: -60 °C
Flash Point: 108 °F
Refractive Index: n20/D 1.454 (lit.)
Viscosity: 1.49 mm²/s
Water Solubility: 10 g/L at 20 °C
Vapor Pressure: 3.6 mm Hg at 20 °C
Storage Temperature: Store below +30 °C
pH: 12 (5 g/L, H₂O, 20 °C)

Explosive Limit: 3.6-19% (V)
Freezing Point: Sensitive: Air sensitive
BRN: 1919922
Dielectric Constant: 2.86
InChIKey: SVYKKECYCPFKGB-UHFFFAOYSA-N
LogP: 2.31 at 25 °C
Safety and Regulatory Information:
FDA UNII: N1H19E7HTA
NIST Chemistry Reference: Cyclohexanamine, N,N-dimethyl- (98-94-2)
EPA Substance Registry System: N,N-Dimethylcyclohexylamine (98-94-2)
Specific Gravity: 0.84900 @ 25.00 °C
Solubility: Water, 1.026e+004 mg/L @ 25 °C (est)



FIRST AID MEASURES of ADDOCAT 726 B:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 726 B:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 726 B:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 726 B:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 726 B:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 726 B:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

ADDOCAT 9727 P
Addocat 9727 P is a high-efficiency sponge amine catalyst with low density (below 10 kg\\\m³), with good performance tolerance and foam stabilization effect, can replace the similar product SMP, which plays the role of amine catalyst.


Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of tertiary amines



Addocat 9727 P is a powerful catalyst for the gas reaction.
Addocat 9727 P is one of the standard catalysts for polyether flexible foam systems (0.10 - 0.15 p.b.w.)
Addocat 9727 P on 100 p.b.w. polyether polyol.


The crosslinking reaction of Addocat 9727 P is catalyzed with Addocat SO (Sn-octoate 0.1 - 0.3 p.b.w.).
Addocat 9727 P is a base catalyst which, to enable the reaction to be more carefully controlled, can be combined with mild co-catalysts, without narrowing the Sn-octoate range.


Addocat 9727 P is a mixture of tertiary amines.
Addocat 9727 P acts as a catalyst for the production of polyurethane foams, e.g. flexible slabstock foam (ether type), hot molded foam, HR foam.
Addocat 9727 P is a base catalyst which, to enable the reaction to be more carefully controlled, can be combined with mild co-catalysts, without narrowing the Sn-octoate range.


For HR foams – based on polymer polyols, for example – Addocat 9727 P can be combined with other strong amines such as Addocat108.
Addocat 9727 P has a shelf-life of 6 months.
Addocat 9727 P is a high-efficiency sponge amine catalyst with low density (below 10 kg\\\m³), with good performance tolerance and foam stabilization effect, can replace the similar product SMP, which plays the role of amine catalyst.


Addocat 9727 P has the ability to increase hardness.
When Addocat 9727 P is mixed with polyether polyol, the storage time of the mixture should not exceed 12 hours. (Use the same day)
Due to the low vapor pressure of Addocat 9727 P, the package should be closed immediately after use to prevent evaporation and deterioration.



USES and APPLICATIONS of ADDOCAT 9727 P:
Addocat 9727 P is used in the production of low-density flexible foam and can provide wide process widths.
Addocat 9727 P is easy to use and can be directly exchanged by customers with the same type of amine catalyst (within 10% dosage difference).


Addocat 9727 P can be directly used for dosing or pre-mixed with polyether, the mixing ratio can be 1:5 to 1:12 or less.
Addocat 9727 P acts as a catalyst for the production of polyurethane foams, e.g. flexible slabstock foam (ether type), hot molded foam, HR foam.


Addocat 9727 P is a base catalyst which, to enable the reaction to be more carefully controlled, can be combined with mild co-catalysts, without narrowing the Sn-octoate range.
For HR foams – based on polymer polyols, for example – Addocat 9727 P can be combined with other strong amines such as Addocat108.



POINTS TO USE OF ADDOCAT 9727 P:
When using Addocat 9727 P, it is recommended to pay attention to the following points:
Addocat 9727 P is recommended to be used as a separate amine catalyst.
Addocat 9727 P is recommended to replace the original amount of amine catalyst used with 1:1 and then fine-tune according to actual needs.
(Addocat 9727 P is recommended that the fine-tuning range be within 10% of the amine dose.)



FUNCTION OF ADDOCAT 9727 P:
Catalyst for the production of polyurethane foams, e.g. flexible slabstock foam (ether type), hot molded foam, HR foam.




PROFILE OF ADDOCAT 9727 P:
Addocat 9727 P is an amine catalyst developed for "dichloromethane formulations" (content >20) suitable for the production of low density (less than 10 kg/m3) foam material.
Addocat 9727 P has high catalytic performance and high catalytic activity.
Compared to conventional amine catalysts, the Addocat 9727 P catalyst provides good working width and foam stabilization during the foaming process.
Compared with the same type of amine catalyst in the market, Catalyst Addocat 9727 P can increase the hardness of mushroom.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT 9727 P:
Product Type: Polymerization Initiators / Inhibitors / Catalysts > Catalysts
Chemical Composition: Mixture of tertiary amines
Physical Form: Liquid



FIRST AID MEASURES of ADDOCAT 9727 P:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT 9727 P:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT 9727 P:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT 9727 P:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT 9727 P:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT 9727 P:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

ADDOCAT DB
Addocat DB is a moderately active gelling biased tertiary amine catalyst.
Addocat DB acts as a catalyst for the production of polyurethane foams, e.g. ester-based flexible slabstock foam and rigid foam.


CAS Number: 103-83-3
EC Number: 203-149-1
chemical composition: tertiary amine
Product Type: Polyurethane-Amine
Molecular formula: C9H13N



SYNONYMS:
Benzenemethanamine,N,N-dimethyl-, Benzylamine,N,N-dimethyl-, N,N-Dimethylbenzenemethanamine, Benzyldimethylamine, Dimethylbenzylamine, N-Benzyldimethylamine, N,N-Dimethyl-N-benzylamine, BDMA,



Addocat DB is tertiary amine.
Addocat DB acts as a catalyst for the production of polyurethane foams, e.g. ester-based flexible slabstock foam and rigid foam.
Addocat DB slightly activates the crosslinking reaction.


Addocat DB has a shelf life of 12 months.
Addocat DB is a polyurethane catalyst based on a tertiary amine, specifically N,N benzyldimethylamine.
Addocat DB is also a good emulsifier for organic compounds.


Addocat DB is a moderately active gelling biased tertiary amine catalyst.
Addocat DB is a catalyst for the production of PUR foams, e. g. flexible ester slabstock foam, hot molded foam, filling foam, rigid foam as well as other PUR applications, e. g. paints and coatings.


Addocat DB is a catalyst for polyester polyurethane block soft foam, polyurethane rigid foam, polyurethane sheet and adhesive coating in polyurethane industry.
Addocat DB is a non-VOC oxygenated solvent for use as a coalescing agent in water-based coatings.
Addocat DB is a proprietary mixture of branched esters of dibasic acids.



USES and APPLICATIONS of ADDOCAT DB:
Addocat DB is often used as a co-catalyst and gives rigid foam a tough and slightly elastic surface, especially in polyester-polyol containing systems.
Addocat DB is used mainly in the continuous production of slab-stock foam with densities higher than 50 kg/m3, on-site casting and continuous production of building boards with flexible and rigid or metal facings.


Addocat DB is used mainly in the continuous production of slab-stock foam with densities higher than 50 kg/m³. Depending on the desired density, Zusatzmittel SM can be used simultaneously (at dosages of 1.0 - 4.0 parts by weight Zusatzmittel SM).
On-site casting: Addocat DB is used continuous production of building boards with flexible and rigid or metal facings.


Addocat DB activates the gelling reaction (cross linking) and is suitable for the production of polyester-based flexible slabstock foam and rigid polyurethane foam.
Addocat DB is a colorless to slightly yellowish, clear liquid


Addocat DB is used in rigid foam systems, activates the blowing and the crosslinking reaction of rigid foam systems.
Addocat DB is used in cold/heat insulation of refrigerators and piping.
Addocat DB is used production of building boards (sandwich panels).


Addocat DB is used in flexible ester slabston foam, it activates the blowing and the crosslinking reaction.
When processing cellular Vulkollan, Addocat DB is added to the crosslinker mixture.
Addocat DB accelerates the drying and curing of 2K PUR coatings based on aliphatic diisocyanates.


In the field of organic synthesis, Addocat DB is mainly used as a catalyst for synthesizing dehydrohalogen in organic drugs, a corrosion inhibitor, an acidic neutralizer, an accelerator for electron microscopy slicing, and the like.
Addocat DB is also used to synthesize quaternary ammonium salts to produce cationic surface active strong fungicides.


Addocat DB is mainly used to promote curing systems such as anhydrides, polyamides, and fatty amines, and accelerates product curing.
Addocat DB is widely used in epoxy resin electronic potting materials, encapsulating materials, epoxy floor coatings, and marine paints.
Addocat DB is used as a curing accelerator.


Addocat DB is also used in floor lacquers, coatings for concrete surfaces and other coatings where high performance is needed.
Addocat DB is mainly used for hard foam, which can make polyurethane foam have good pre-flowability and uniform cells.
Good adhesion between the foam and the substrate.


Addocat DB is mostly used as a co-catalyst and gives rigid foam a tough and slightly elastic surface, esp. in polyester
polyol containing systems.
Addocat DB is used flexible ester slabstock foam.


Addocat DB can be used as main catalyst for the production of flexible ester foam based mainly on TDI 65/35.
Addocat DB is used at 1.0 - 1.6 pphp, depending on the water content of the formulation (2.0 - 5.0 pphp).
Since Addocat DB is insoluble in water, it can be emulsified in a mixture of water.


-Flexible slabstock foam (ester-based):
Addocat DB is an activator for the production of flexible polyester foam based mainly on TDI 65/35.
1.0 - 1.6 parts by weight Addocat DB, calculated on 100 parts by weight polyester polyol, are used, depending on the water content of the formulation (2.0 - 5.0 parts by weight water).
Since Addocat DB is insoluble in water, it can be emulsified in a mixture of water, Dispergiermittel WM and Zusatzmittel SM.


-Rigid polyurethane foam:
Addocat DB slightly activates the crosslinking reaction.
Addocat DB is often used as a co-catalyst and gives rigid foam a tough and slightly elastic surface, especially in polyester-polyol containing systems.


-Rigid foam uses of Addocat DB:
• Continuous production of slabstock foam with densities higher than 50 kg/m³
• Continuous production of building boards with flexible and rigid or metal facings
• On-site casting



FUNCTION OF ADDOCAT DB:
Catalyst for the production of polyurethane foams, e.g. ester-based flexible slabstock foam and rigid foam.



BENEFITS OF ADDOCAT DB:
*Non-VOC
*Nearly odourless
*Higher efficiency compared to typical coalescing agents
*Early block, rain, and chemical resistance
*No labelling
*Readily biodegradable



STORAGE CONDITIONS OF ADDOCAT DB:
Addocat DB is to be stored in a cool and dry place.
In firmly closed original containers at dry conditions at approx. 20°C, a shelf-life of 24 months from manufacturing date can be expected.
Prolonged Addocat DB storage, esp. at temperatures above 30 °C, may lead to discoloration even in closed containers.
This does not have a negative impact on catalytic activity.
The containers should be resealed tightly after use to prevent exposure to moisture and impurities.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT DB:
Active ingredient content min. 99.3 %
Color number max. 25 HU
Density at 20 °C approx 0.90 g/cm³
Flash point approx. 60 °C
Initial boiling point approx. 180 °C
Pour point < - 70 °C
Viscosity approx. 26 mPa·s
Water content max. 0.15 %
Molecular formula: C9H13N;
Relative molecular mass: 135.20;
CAS number: 103-83-3;

Colorless to slightly yellow transparent liquid, soluble in ethanol,
soluble in hot water, slightly soluble in cold water;
Purity ≥99%;
Moisture ≤ 0.5%;
Viscosity (25 ° C): 90 mPa.s;
Density (25 ° C): 0.897 g / cm 3;
Freezing point: -75 ° C;
Boiling range: 178-184 ° C;
Refractive index (25 ° C): 1.5011;
Flash point (TCC): 54 ° C;
Steam pressure (20 ° C): 200Pa
Product Type: Crosslinking Catalysts / Accelerators / Initiators > Amine or Nitrogen Content
Chemical Composition: Tertiary amine
Masterbatch: No



FIRST AID MEASURES of ADDOCAT DB:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT DB:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT DB:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT DB:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT DB:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT DB:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT PP
Addocat PP is a blend of tertiary amines.
Addocat PP acts as a catalyst.


CAS Number: 104-19-8;3030-47-5
Product Type: Polyurethane-Amine
Product Type: Catalysts / Accelerators / Initiators > Amines
Chemical Composition: Blend of tertiary amines


SYNONYMS:
Dabco RP205, Addocat 9727P, High Performance Amine Catalyst, Dabco Amine Catalyst, Dabco RP205 Low Density Sponge Catalyst



Addocat PP is a blend of tertiary amines.
Addocat PP acts as a catalyst.
Addocat PP's addition reduces the potlife of the finish.


To give greater convenience and accuracy of dosage.
Addocat PP's recommended dosage is 0.02 to 0.50 % calculated on the total amount of Desmodur/Desmophen.
Addocat PP has a shelf life of 12 months.


Addocat PP is a polyurethane catalyst based on a blend of tertiary amines.
Addocat PP is a catalyst for the production of PUR foams, e. g. flexible ester slabstock foam, hot molded foam, filling foam, rigid foam as well as other PUR applications, e. g. paints and coatings.


Addocat PP is a colorless to slightly yellowish, clear liquid.
Addocat PP accelerates the drying and curing of 2-component polyurethane coatings based on aliphatic diisocyanates such as e.g.
Desmodur N-types or Desmodur Z 4470 and polyols of the Desmophen series.


The addition of Addocat PP reduces the pot life of the finish.
To give greater convenience and accuracy of dosage.
The added quantity of Addocat PP is approx. 0.02 to 0.50% calculated on the total amount of Desmodur/Desmophen.
The optimum dosage of Addocat PP should be determined by trials.



USES and APPLICATIONS of ADDOCAT PP:
Addocat PP is used in rigid foam systems, activates the blowing and the crosslinking reaction of rigid foam systems.
Addocat PP is used cold/heat insulation of refrigerators and piping.
Addocat PP is used production of building boards (sandwich panels).


Addocat PP is used in flexible ester slab stone foam,
Addocat PP activates the blowing and the crosslinking reaction.
When processing cellular Vulkollan, Addocat PP is added to the crosslinker mixture.


Addocat PP accelerates the drying and curing of 2K PUR coatings based on aliphatic diisocyanates.
Addocat PP is used Polymer auxiliaries
Addocat PP is specifically recommended for use in polyurethane coatings based on aliphatic diisocyanates.


Addocat PP accelerates the drying and curing of 2K polyurethane coatings.
Addocat PP should be used as a 10% solution in solvents such as butyl acetate, ethyl acetate, methylisobutylketone, methylethylketone or xylene.


Addocat PP acelerates the drying and curing of 2-component polyurethane coatings based on aliphatic diisocyanates such as e.g. Desmodur N-types or Desmodur Z 4470 and polyols of the Desmophen series.
Addocat PP should be used as a 10% solution in solvents such as butyl acetate, ethyl acetate, methylisobutylketone, methylethylketone or xylene.



FUNCTION OF ADDOCAT PP:
Catalyst for polyurethane coatings



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT PP:
Product Type: Catalysts / Accelerators / Initiators > Amines
Chemical Composition: Blend of tertiary amines
Physical Form: Liquid



FIRST AID MEASURES of ADDOCAT PP:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT PP:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT PP:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT PP:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT PP:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT PP:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOCAT SO
Addocat SO is stannous (II) ethylhexanoate.
Addocat SO is a basic catalyst used in the production of polyurethane foam, room temperature curing silicone rubber, polyurethane rubber, and polyurethane coatings.


CAS Number: 301-10-0
chemical composition: stannous (II) ethylhexanoate (stannous(II)octoate)
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical formula C16H30O4Sn



SYNONYMS:
Stannous octoate, Stannous octoate, DABCO T-9, Kosmos 29, Addocat SO, Niax D-19, PC CAT T9, Borchi Kat 28, CAS 301-10-0, dabco t catalyst, dabco t urethane catalyst, stannous octoate D19, stannous octoate T- 9, Gel Catalyst T-9, Organotin T-9, Stannous octoate, Stannous octoate, DABCO T-9, Kosmos 29, Addocat SO, Niax D-19, PC CAT T9, Borchi Kat 28, CAS 301-10-0, dabco t catalyst, dabco t polyurethane catalyst, Hexanoic acid,2-ethyl-,tin(2+) salt (2:1), Hexanoic acid,2-ethyl-,tin(2+) salt, Stannous 2-ethylhexanoate, Stannous 2-ethylhexoate, Tin(II) 2-ethylhexanoate, Tin(2+) 2-ethylhexanoate, Nuocure 28, Stannous octoate, Tin octoate, Tin dioctoate, Tin bis(2-ethylcaproate), Stannous 2-ethylcaproate, T 10 (catalyst), T 10, Tin bis(2-ethylhexanoate), T 9, Cata-Chek 860, Fascat 2003, D 19, Stanoct T 90, Dabco T 16, Stannous(II) ethylhexanoate, Stannous dioctanoate, Neostann U 28, Stannous octanoate, Stannous caprylate, Stanoct, Kosmos 29, K 29, Dabco T 9, Tegokat 129, PC CAT T 9, U 28, XY 70, HMT 9, Dabco T 10, Bis(2-ethylhexanoate) tin, NSC 75857, 2-Ethylhexanoic acid tin(2+) salt, Desmorapid SO, Kosmos K 5N, KCS 405T, S 93-5037, T-Cat 110, Niax D 19, BTN-Cat 110, Dabco DC 21, XY 70 (catalyst), Neostann E 80, Addocat SO, Kosmos 10P, Borchi Kat 28, K 5N, Reaxis C 129, Metacure T 9, Stannous iosoctanoate, B 23612, T 19, PUB 350, T 9 (catalyst), Menhover S 19, Menhover Tin S 19, S 19, A 67510, 75831-41-3, 2417629-16-2



Addocat SO is a basic catalyst used in the production of polyurethane foam, room temperature curing silicone rubber, polyurethane rubber, and polyurethane coatings.
Addocat SO is chemically unstable and easily oxidized.


Addocat SO is a white or light yellow-brown paste, sometimes called stannous octoate.
Addocat SO is soluble in petroleum ether and insoluble in water.
Addocat SO is stannous (II) ethylhexanoate.


Addocat SO acts as a catalyst for the production of polyurethanes, e.g. polyether and polyester flexible slabstock foam, hot molded foam, rigid spray foam.
Addocat SO catalyzes mainly the crosslinking reaction of the polyol and isocyanates.
Recommended dosage of Addocat SO is between 0.03 and 0.5 p.b.w.


Addocat SO has a shelf life of 12 months.
Addocat SO catalyses mainly the crosslinking reaction of the polyol and isocyanate.
In the production of polyether and polyester foam Addocat SO is metered separately.


As well as having other advantages of Addocat SO, this enables equilibrium of the crosslinking and gas formation reactions to be maintained during production.
The addition of Addocat SO is normally between 0.03 and 0.5 p.b.w.


The accuracy of metering can be improved if Addocat SO is mixed with other components at a ratio suitable to the capacity of the metering pump, e.g. with polymeric plasticizers that do not affect the polyurethane reaction or with polyether polyols based on propyleneoxide, but without ethylene oxide.
The mixing ratio applicable to these examples is usually 1 : 4 or 1 : 9.


Addocat SO is a polyurethane catalyst based on an organic metal compound, specifically Stannous Octoate.
Addocat SO activates the gelling (crosslinking) reaction in polyether- and polyester-based polyurethane flexible slabstock foam, hot molded foam, rigid spray foam, 2K polyurethane coatings and other polyurethane applications.
Addocat SO is a white or of- white powder or crystlline power,odorless



USES and APPLICATIONS of ADDOCAT SO:
Addocat SO is a basic catalyst for the production of polyurethane foam plastics, mainly used in the gelling reaction during polyether-polyurethane foaming, and can also be used as an antioxidant for urethane foam plastics.
Addocat SO is used in organic synthesis.


Addocat SO is a basic catalyst used in the production of polyurethane foam, room temperature curing silicone rubber, polyurethane rubber, and polyurethane coatings.
Addocat SO is chemically unstable and easily oxidized.


As well as having other advantages of Addocat SO, this enables equilibrium of the crosslinking and gas formation reactions to be maintained during production.
The addition of Addocat SO is normally between 0.03 and 0.5 p.b.w.


The accuracy of metering can be improved if Addocat SO is mixed with other components at a ratio suitable to the capacity of the metering pump, e.g. with polymeric plasticizers that do not affect the polyurethane reaction or with polyether polyols based on propyleneoxide, but without ethylene oxide.
The mixing ratio applicable to these examples is usually 1 : 4 or 1 : 9.



SOLUBILITY OF ADDOCAT SO:
Addocat SO is very soluble in N,N-Dimethylformamide,
Addocat SO is soluble in methanol,
Addocat SO is sparingly soluble inglacial acetic acid,
Addocat SO is very slightly soluble inchloroform, Practically insoluble in water.



FUNCTION OF ADDOCAT SO:
Catalyst for the production of polyurethanes, e.g. polyether and polyester flexible slabstock foam, hot molded foam, rigid spray foam, 2 C-paints and coatings as well as other polyurethane applications.



PHYSICAL and CHEMICAL PROPERTIES of ADDOCAT SO:
Product Type: Crosslinking Catalysts / Accelerators / Initiators
Chemical Composition: Stannous (II) ethylhexanoate
Chemical English Name: Stannous octoate
CAS Number: 301-10-0
Molecular Formula: C16H30O4Sn
Molecular Formula (Alternate): C8H16O2.1/2Sn
Molecular Weight: 405.10 g/mol
Exact Mass: 406.116608 g/mol
EC Number: 206-108-6
DSSTox ID: DTXSID1027138

HS Code: 29159000
Categories: Bulk Drug Intermediates
InChIKey: BOZRCGLDOHDZBP-UHFFFAOYSA-N
Physical Properties:
Physical Form: Liquid
Appearance and Properties: White or yellow paste
Relative Density (water = 1): 1.251
Density: 1.251 g/cm³
Density (alternate): 1.28 g/cm³
Melting Point: 34 °C
Freezing Point: -20 °C
Boiling Point: >200 °C

Flash Point: >110 °C
Viscosity (25 °C): ≤380 MPa·s
Refractive Index: n20/D 1.492 (lit.), n20/D 1.493 (lit.)
Solubility: Insoluble in water, soluble in petroleum ether and polyols
Water Solubility: Miscible with water
Corrosiveness: Non-corrosive
Chemical Properties:
Main Content of Stannous Metal: 28 +/- 0.50%
PSA (Polar Surface Area): 80.26000 Ų
XLogP3: 1.52460



FIRST AID MEASURES of ADDOCAT SO:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of ADDOCAT SO:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADDOCAT SO:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADDOCAT SO:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADDOCAT SO:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of ADDOCAT SO:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


ADDOLINK 1604

Addolink 1604 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1604 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink 1604 is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 68479-98-1
EC Number: 270-877-4

Synonyms: Polyurethane crosslinker, Addolink 1604, Crosslinker 1604, Addolink Polyurethane Crosslinker 1604, PU Crosslinker 1604, Polyurethane Additive 1604, Crosslinking Agent 1604, Additive 1604, PU Additive 1604, Addolink PU Crosslinker 1604



APPLICATIONS


Addolink 1604 is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink 1604 is essential in the manufacture of high-performance polyurethane adhesives.
Addolink 1604 is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink 1604 is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink 1604 is used in automotive coatings for its excellent adhesion and flexibility.
Addolink 1604 is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink 1604 is used in water-based polyurethane systems for its compatibility and stability.
Addolink 1604 is a key component in solvent-based polyurethane coatings.
Addolink 1604 is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink 1604 is employed in the production of rubber materials for its crosslinking properties.
Addolink 1604 is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink 1604 is used in the construction industry for high-performance coatings and sealants.

Addolink 1604 is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink 1604 is a key component in the production of plastics, improving their mechanical properties.
Addolink 1604 is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink 1604 is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink 1604 is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink 1604 is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink 1604 is used in the production of rubber products, ensuring durable and consistent performance.
Addolink 1604 is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink 1604 is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink 1604 is found in the manufacture of specialty coatings for industrial machinery.
Addolink 1604 is utilized in the formulation of adhesives and sealants.
Addolink 1604 is a key ingredient in the production of polyurethane elastomers.

Addolink 1604 is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink 1604 is used in the rubber industry for its crosslinking properties.
Addolink 1604 is essential in the production of high-performance industrial coatings.

Addolink 1604 is a vital component in water-based and solvent-based polyurethane systems.
Addolink 1604 is applied in the creation of high-performance industrial products.
Addolink 1604 is used in the formulation of household and industrial coatings.

Addolink 1604 is utilized in the production of specialty coatings for electronic devices.
Addolink 1604 is found in the creation of specialty inks for various applications.
Addolink 1604 is used in the production of ceramic and glass coatings.

Addolink 1604 is applied in the creation of coatings for plastic surfaces.
Addolink 1604 is utilized in the formulation of coatings for wood surfaces.
Addolink 1604 is essential in the production of high-performance adhesives.

Addolink 1604 is used in the formulation of coatings for automotive applications.
Addolink 1604 is utilized in the production of specialty adhesives and sealants.
Addolink 1604 is found in the manufacture of coatings for industrial machinery.

Addolink 1604 is employed in the creation of specialty coatings for various substrates.
Addolink 1604 is used in the formulation of high-performance coatings for various applications.
Addolink 1604 is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink 1604 is used in the creation of specialty inks for digital printing.
Addolink 1604 is essential in the production of high-performance industrial products.
Addolink 1604 is utilized in the manufacture of environmentally friendly industrial products.

Addolink 1604 is used in the creation of water-based and solvent-based products.
Addolink 1604 is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink 1604 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1604 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink 1604 is a versatile chemical compound used in various polyurethane applications.
Addolink 1604 is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink 1604 provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink 1604 is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink 1604 is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink 1604's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink 1604 offers excellent weather resistance, making it suitable for outdoor applications.
Addolink 1604 is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink 1604 is essential in the creation of durable and high-performance polyurethane products.

Addolink 1604's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink 1604 is an important precursor in the production of high-performance adhesives and sealants.
Addolink 1604 is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink 1604
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink 1604 is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink 1604.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink 1604 in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink 1604 at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink 1604 away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink 1604 to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOLINK 1701

Addolink 1701 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1701 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink 1701 is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 69102-90-5
EC Number: 614-424-4

Synonyms: Polyurethane crosslinker, Addolink 1701, Crosslinker 1701, Addolink Polyurethane Crosslinker 1701, PU Crosslinker 1701, Polyurethane Additive 1701, Crosslinking Agent 1701, Additive 1701, PU Additive 1701, Addolink PU Crosslinker 1701



APPLICATIONS


Addolink 1701 is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink 1701 is essential in the manufacture of high-performance polyurethane adhesives.
Addolink 1701 is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink 1701 is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink 1701 is used in automotive coatings for its excellent adhesion and flexibility.
Addolink 1701 is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink 1701 is used in water-based polyurethane systems for its compatibility and stability.
Addolink 1701 is a key component in solvent-based polyurethane coatings.
Addolink 1701 is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink 1701 is employed in the production of rubber materials for its crosslinking properties.
Addolink 1701 is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink 1701 is used in the construction industry for high-performance coatings and sealants.

Addolink 1701 is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink 1701 is a key component in the production of plastics, improving their mechanical properties.
Addolink 1701 is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink 1701 is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink 1701 is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink 1701 is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink 1701 is used in the production of rubber products, ensuring durable and consistent performance.
Addolink 1701 is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink 1701 is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink 1701 is found in the manufacture of specialty coatings for industrial machinery.
Addolink 1701 is utilized in the formulation of adhesives and sealants.
Addolink 1701 is a key ingredient in the production of polyurethane elastomers.

Addolink 1701 is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink 1701 is used in the rubber industry for its crosslinking properties.
Addolink 1701 is essential in the production of high-performance industrial coatings.

Addolink 1701 is a vital component in water-based and solvent-based polyurethane systems.
Addolink 1701 is applied in the creation of high-performance industrial products.
Addolink 1701 is used in the formulation of household and industrial coatings.

Addolink 1701 is utilized in the production of specialty coatings for electronic devices.
Addolink 1701 is found in the creation of specialty inks for various applications.
Addolink 1701 is used in the production of ceramic and glass coatings.

Addolink 1701 is applied in the creation of coatings for plastic surfaces.
Addolink 1701 is utilized in the formulation of coatings for wood surfaces.
Addolink 1701 is essential in the production of high-performance adhesives.

Addolink 1701 is used in the formulation of coatings for automotive applications.
Addolink 1701 is utilized in the production of specialty adhesives and sealants.
Addolink 1701 is found in the manufacture of coatings for industrial machinery.

Addolink 1701 is employed in the creation of specialty coatings for various substrates.
Addolink 1701 is used in the formulation of high-performance coatings for various applications.
Addolink 1701 is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink 1701 is used in the creation of specialty inks for digital printing.
Addolink 1701 is essential in the production of high-performance industrial products.
Addolink 1701 is utilized in the manufacture of environmentally friendly industrial products.

Addolink 1701 is used in the creation of water-based and solvent-based products.
Addolink 1701 is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink 1701 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1701 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink 1701 is a versatile chemical compound used in various polyurethane applications.
Addolink 1701 is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink 1701 provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink 1701 is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink 1701 is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink 1701's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink 1701 offers excellent weather resistance, making it suitable for outdoor applications.
Addolink 1701 is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink 1701 is essential in the creation of durable and high-performance polyurethane products.

Addolink 1701's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink 1701 is an important precursor in the production of high-performance adhesives and sealants.
Addolink 1701 is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink 1701
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink 1701 is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink 1701.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink 1701 in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink 1701 at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink 1701 away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink 1701 to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOLINK 1705

Addolink 1705 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1705 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink 1705 is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 69102-90-5
EC Number: 614-424-4

Synonyms: Polyurethane crosslinker, Addolink 1705, Crosslinker 1705, Addolink Polyurethane Crosslinker 1705, PU Crosslinker 1705, Polyurethane Additive 1705, Crosslinking Agent 1705, Additive 1705, PU Additive 1705, Addolink PU Crosslinker 1705



APPLICATIONS


Addolink 1705 is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink 1705 is essential in the manufacture of high-performance polyurethane adhesives.
Addolink 1705 is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink 1705 is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink 1705 is used in automotive coatings for its excellent adhesion and flexibility.
Addolink 1705 is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink 1705 is used in water-based polyurethane systems for its compatibility and stability.
Addolink 1705 is a key component in solvent-based polyurethane coatings.
Addolink 1705 is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink 1705 is employed in the production of rubber materials for its crosslinking properties.
Addolink 1705 is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink 1705 is used in the construction industry for high-performance coatings and sealants.

Addolink 1705 is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink 1705 is a key component in the production of plastics, improving their mechanical properties.
Addolink 1705 is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink 1705 is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink 1705 is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink 1705 is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink 1705 is used in the production of rubber products, ensuring durable and consistent performance.
Addolink 1705 is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink 1705 is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink 1705 is found in the manufacture of specialty coatings for industrial machinery.
Addolink 1705 is utilized in the formulation of adhesives and sealants.
Addolink 1705 is a key ingredient in the production of polyurethane elastomers.

Addolink 1705 is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink 1705 is used in the rubber industry for its crosslinking properties.
Addolink 1705 is essential in the production of high-performance industrial coatings.

Addolink 1705 is a vital component in water-based and solvent-based polyurethane systems.
Addolink 1705 is applied in the creation of high-performance industrial products.
Addolink 1705 is used in the formulation of household and industrial coatings.

Addolink 1705 is utilized in the production of specialty coatings for electronic devices.
Addolink 1705 is found in the creation of specialty inks for various applications.
Addolink 1705 is used in the production of ceramic and glass coatings.

Addolink 1705 is applied in the creation of coatings for plastic surfaces.
Addolink 1705 is utilized in the formulation of coatings for wood surfaces.
Addolink 1705 is essential in the production of high-performance adhesives.

Addolink 1705 is used in the formulation of coatings for automotive applications.
Addolink 1705 is utilized in the production of specialty adhesives and sealants.
Addolink 1705 is found in the manufacture of coatings for industrial machinery.

Addolink 1705 is employed in the creation of specialty coatings for various substrates.
Addolink 1705 is used in the formulation of high-performance coatings for various applications.
Addolink 1705 is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink 1705 is used in the creation of specialty inks for digital printing.
Addolink 1705 is essential in the production of high-performance industrial products.
Addolink 1705 is utilized in the manufacture of environmentally friendly industrial products.

Addolink 1705 is used in the creation of water-based and solvent-based products.
Addolink 1705 is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink 1705 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 1705 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink 1705 is a versatile chemical compound used in various polyurethane applications.
Addolink 1705 is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink 1705 provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink 1705 is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink 1705 is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink 1705's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink 1705 offers excellent weather resistance, making it suitable for outdoor applications.
Addolink 1705 is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink 1705 is essential in the creation of durable and high-performance polyurethane products.

Addolink 1705's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink 1705 is an important precursor in the production of high-performance adhesives and sealants.
Addolink 1705 is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink 1705
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink 1705 is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink 1705.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink 1705 in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink 1705 at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink 1705 away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink 1705 to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.








ADDOLINK 9823

Addolink 9823 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 9823 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink 9823 is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 2425-79-8
EC Number: 219-371-7

Synonyms: Polyurethane crosslinker, Addolink 9823, Crosslinker 9823, Addolink Polyurethane Crosslinker 9823, PU Crosslinker 9823, Polyurethane Additive 9823, Crosslinking Agent 9823, Additive 9823, PU Additive 9823, Addolink PU Crosslinker 9823



APPLICATIONS


Addolink 9823 is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink 9823 is essential in the manufacture of high-performance polyurethane adhesives.
Addolink 9823 is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink 9823 is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink 9823 is used in automotive coatings for its excellent adhesion and flexibility.
Addolink 9823 is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink 9823 is used in water-based polyurethane systems for its compatibility and stability.
Addolink 9823 is a key component in solvent-based polyurethane coatings.
Addolink 9823 is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink 9823 is employed in the production of rubber materials for its crosslinking properties.
Addolink 9823 is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink 9823 is used in the construction industry for high-performance coatings and sealants.

Addolink 9823 is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink 9823 is a key component in the production of plastics, improving their mechanical properties.
Addolink 9823 is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink 9823 is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink 9823 is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink 9823 is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink 9823 is used in the production of rubber products, ensuring durable and consistent performance.
Addolink 9823 is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink 9823 is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink 9823 is found in the manufacture of specialty coatings for industrial machinery.
Addolink 9823 is utilized in the formulation of adhesives and sealants.
Addolink 9823 is a key ingredient in the production of polyurethane elastomers.

Addolink 9823 is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink 9823 is used in the rubber industry for its crosslinking properties.
Addolink 9823 is essential in the production of high-performance industrial coatings.

Addolink 9823 is a vital component in water-based and solvent-based polyurethane systems.
Addolink 9823 is applied in the creation of high-performance industrial products.
Addolink 9823 is used in the formulation of household and industrial coatings.

Addolink 9823 is utilized in the production of specialty coatings for electronic devices.
Addolink 9823 is found in the creation of specialty inks for various applications.
Addolink 9823 is used in the production of ceramic and glass coatings.

Addolink 9823 is applied in the creation of coatings for plastic surfaces.
Addolink 9823 is utilized in the formulation of coatings for wood surfaces.
Addolink 9823 is essential in the production of high-performance adhesives.

Addolink 9823 is used in the formulation of coatings for automotive applications.
Addolink 9823 is utilized in the production of specialty adhesives and sealants.
Addolink 9823 is found in the manufacture of coatings for industrial machinery.

Addolink 9823 is employed in the creation of specialty coatings for various substrates.
Addolink 9823 is used in the formulation of high-performance coatings for various applications.
Addolink 9823 is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink 9823 is used in the creation of specialty inks for digital printing.
Addolink 9823 is essential in the production of high-performance industrial products.
Addolink 9823 is utilized in the manufacture of environmentally friendly industrial products.

Addolink 9823 is used in the creation of water-based and solvent-based products.
Addolink 9823 is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink 9823 is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink 9823 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink 9823 is a versatile chemical compound used in various polyurethane applications.
Addolink 9823 is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink 9823 provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink 9823 is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink 9823 is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink 9823's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink 9823 offers excellent weather resistance, making it suitable for outdoor applications.
Addolink 9823 is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink 9823 is essential in the creation of durable and high-performance polyurethane products.

Addolink 9823's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink 9823 is an important precursor in the production of high-performance adhesives and sealants.
Addolink 9823 is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink 9823
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink 9823 is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink 9823.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink 9823 in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink 9823 at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink 9823 away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink 9823 to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.



ADDOLINK B

Addolink B is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink B is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink B is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 9003-36-5
EC Number: 500-006-8

Synonyms: Polyurethane crosslinker, Addolink B, Crosslinker B, Addolink Polyurethane Crosslinker, PU Crosslinker, Polyurethane Additive, Crosslinking Agent B, Additive B, PU Additive B, Addolink PU Crosslinker



APPLICATIONS


Addolink B is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink B is essential in the manufacture of high-performance polyurethane adhesives.
Addolink B is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink B is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink B is used in automotive coatings for its excellent adhesion and flexibility.
Addolink B is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink B is used in water-based polyurethane systems for its compatibility and stability.
Addolink B is a key component in solvent-based polyurethane coatings.
Addolink B is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink B is employed in the production of rubber materials for its crosslinking properties.
Addolink B is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink B is used in the construction industry for high-performance coatings and sealants.

Addolink B is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink B is a key component in the production of plastics, improving their mechanical properties.
Addolink B is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink B is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink B is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink B is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink B is used in the production of rubber products, ensuring durable and consistent performance.
Addolink B is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink B is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink B is found in the manufacture of specialty coatings for industrial machinery.
Addolink B is utilized in the formulation of adhesives and sealants.
Addolink B is a key ingredient in the production of polyurethane elastomers.

Addolink B is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink B is used in the rubber industry for its crosslinking properties.
Addolink B is essential in the production of high-performance industrial coatings.

Addolink B is a vital component in water-based and solvent-based polyurethane systems.
Addolink B is applied in the creation of high-performance industrial products.
Addolink B is used in the formulation of household and industrial coatings.

Addolink B is utilized in the production of specialty coatings for electronic devices.
Addolink B is found in the creation of specialty inks for various applications.
Addolink B is used in the production of ceramic and glass coatings.

Addolink B is applied in the creation of coatings for plastic surfaces.
Addolink B is utilized in the formulation of coatings for wood surfaces.
Addolink B is essential in the production of high-performance adhesives.

Addolink B is used in the formulation of coatings for automotive applications.
Addolink B is utilized in the production of specialty adhesives and sealants.
Addolink B is found in the manufacture of coatings for industrial machinery.

Addolink B is employed in the creation of specialty coatings for various substrates.
Addolink B is used in the formulation of high-performance coatings for various applications.
Addolink B is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink B is used in the creation of specialty inks for digital printing.
Addolink B is essential in the production of high-performance industrial products.
Addolink B is utilized in the manufacture of environmentally friendly industrial products.

Addolink B is used in the creation of water-based and solvent-based products.
Addolink B is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink B is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink B is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink B is a versatile chemical compound used in various polyurethane applications.
Addolink B is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink B provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink B is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink B is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink B's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink B offers excellent weather resistance, making it suitable for outdoor applications.
Addolink B is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink B is essential in the creation of durable and high-performance polyurethane products.

Addolink B's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink B is an important precursor in the production of high-performance adhesives and sealants.
Addolink B is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink B
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink B is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink B.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink B in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink B at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink B away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink B to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOLINK H EP

Addolink H EP is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink H EP is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink H EP is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 25214-63-5
EC Number: 246-771-9

Synonyms: Polyurethane crosslinker, Addolink H EP, Crosslinker H EP, Addolink Polyurethane Crosslinker H EP, PU Crosslinker H EP, Polyurethane Additive H EP, Crosslinking Agent H EP, Additive H EP, PU Additive H EP, Addolink PU Crosslinker H EP



APPLICATIONS


Addolink H EP is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink H EP is essential in the manufacture of high-performance polyurethane adhesives.
Addolink H EP is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink H EP is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink H EP is used in automotive coatings for its excellent adhesion and flexibility.
Addolink H EP is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink H EP is used in water-based polyurethane systems for its compatibility and stability.
Addolink H EP is a key component in solvent-based polyurethane coatings.
Addolink H EP is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink H EP is employed in the production of rubber materials for its crosslinking properties.
Addolink H EP is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink H EP is used in the construction industry for high-performance coatings and sealants.

Addolink H EP is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink H EP is a key component in the production of plastics, improving their mechanical properties.
Addolink H EP is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink H EP is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink H EP is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink H EP is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink H EP is used in the production of rubber products, ensuring durable and consistent performance.
Addolink H EP is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink H EP is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink H EP is found in the manufacture of specialty coatings for industrial machinery.
Addolink H EP is utilized in the formulation of adhesives and sealants.
Addolink H EP is a key ingredient in the production of polyurethane elastomers.

Addolink H EP is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink H EP is used in the rubber industry for its crosslinking properties.
Addolink H EP is essential in the production of high-performance industrial coatings.

Addolink H EP is a vital component in water-based and solvent-based polyurethane systems.
Addolink H EP is applied in the creation of high-performance industrial products.
Addolink H EP is used in the formulation of household and industrial coatings.

Addolink H EP is utilized in the production of specialty coatings for electronic devices.
Addolink H EP is found in the creation of specialty inks for various applications.
Addolink H EP is used in the production of ceramic and glass coatings.

Addolink H EP is applied in the creation of coatings for plastic surfaces.
Addolink H EP is utilized in the formulation of coatings for wood surfaces.
Addolink H EP is essential in the production of high-performance adhesives.

Addolink H EP is used in the formulation of coatings for automotive applications.
Addolink H EP is utilized in the production of specialty adhesives and sealants.
Addolink H EP is found in the manufacture of coatings for industrial machinery.

Addolink H EP is employed in the creation of specialty coatings for various substrates.
Addolink H EP is used in the formulation of high-performance coatings for various applications.
Addolink H EP is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink H EP is used in the creation of specialty inks for digital printing.
Addolink H EP is essential in the production of high-performance industrial products.
Addolink H EP is utilized in the manufacture of environmentally friendly industrial products.

Addolink H EP is used in the creation of water-based and solvent-based products.
Addolink H EP is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink H EP is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink H EP is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink H EP is a versatile chemical compound used in various polyurethane applications.
Addolink H EP is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink H EP provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink H EP is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink H EP is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink H EP's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink H EP offers excellent weather resistance, making it suitable for outdoor applications.
Addolink H EP is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink H EP is essential in the creation of durable and high-performance polyurethane products.

Addolink H EP's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink H EP is an important precursor in the production of high-performance adhesives and sealants.
Addolink H EP is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink H EP
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink H EP is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink H EP.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink H EP in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink H EP at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink H EP away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink H EP to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

ADDOLINK THPE

Addolink THPE is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink THPE is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink THPE is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 115-77-5
EC Number: 204-104-9

Synonyms: Polyurethane crosslinker, Addolink THPE, Crosslinker THPE, Addolink Polyurethane Crosslinker THPE, PU Crosslinker THPE, Polyurethane Additive THPE, Crosslinking Agent THPE, Additive THPE, PU Additive THPE, Addolink PU Crosslinker THPE



APPLICATIONS


Addolink THPE is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink THPE is essential in the manufacture of high-performance polyurethane adhesives.
Addolink THPE is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink THPE is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink THPE is used in automotive coatings for its excellent adhesion and flexibility.
Addolink THPE is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink THPE is used in water-based polyurethane systems for its compatibility and stability.
Addolink THPE is a key component in solvent-based polyurethane coatings.
Addolink THPE is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink THPE is employed in the production of rubber materials for its crosslinking properties.
Addolink THPE is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink THPE is used in the construction industry for high-performance coatings and sealants.

Addolink THPE is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink THPE is a key component in the production of plastics, improving their mechanical properties.
Addolink THPE is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink THPE is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink THPE is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink THPE is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink THPE is used in the production of rubber products, ensuring durable and consistent performance.
Addolink THPE is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink THPE is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink THPE is found in the manufacture of specialty coatings for industrial machinery.
Addolink THPE is utilized in the formulation of adhesives and sealants.
Addolink THPE is a key ingredient in the production of polyurethane elastomers.

Addolink THPE is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink THPE is used in the rubber industry for its crosslinking properties.
Addolink THPE is essential in the production of high-performance industrial coatings.

Addolink THPE is a vital component in water-based and solvent-based polyurethane systems.
Addolink THPE is applied in the creation of high-performance industrial products.
Addolink THPE is used in the formulation of household and industrial coatings.

Addolink THPE is utilized in the production of specialty coatings for electronic devices.
Addolink THPE is found in the creation of specialty inks for various applications.
Addolink THPE is used in the production of ceramic and glass coatings.

Addolink THPE is applied in the creation of coatings for plastic surfaces.
Addolink THPE is utilized in the formulation of coatings for wood surfaces.
Addolink THPE is essential in the production of high-performance adhesives.

Addolink THPE is used in the formulation of coatings for automotive applications.
Addolink THPE is utilized in the production of specialty adhesives and sealants.
Addolink THPE is found in the manufacture of coatings for industrial machinery.

Addolink THPE is employed in the creation of specialty coatings for various substrates.
Addolink THPE is used in the formulation of high-performance coatings for various applications.
Addolink THPE is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink THPE is used in the creation of specialty inks for digital printing.
Addolink THPE is essential in the production of high-performance industrial products.
Addolink THPE is utilized in the manufacture of environmentally friendly industrial products.

Addolink THPE is used in the creation of water-based and solvent-based products.
Addolink THPE is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink THPE is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink THPE is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink THPE is a versatile chemical compound used in various polyurethane applications.
Addolink THPE is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink THPE provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink THPE is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink THPE is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink THPE's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink THPE offers excellent weather resistance, making it suitable for outdoor applications.
Addolink THPE is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink THPE is essential in the creation of durable and high-performance polyurethane products.

Addolink THPE's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink THPE is an important precursor in the production of high-performance adhesives and sealants.
Addolink THPE is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink THPE
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.2 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink THPE is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink THPE.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink THPE in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink THPE at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink THPE away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink THPE to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOLINK TT
Addolink TT is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink TT is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addolink TT is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 2425-79-8
EC Number: 219-371-7

Synonyms: Polyurethane crosslinker, Addolink TT, Crosslinker TT, Addolink Polyurethane Crosslinker TT, PU Crosslinker TT, Polyurethane Additive TT, Crosslinking Agent TT, Additive TT, PU Additive TT, Addolink PU Crosslinker TT



APPLICATIONS


Addolink TT is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addolink TT is essential in the manufacture of high-performance polyurethane adhesives.
Addolink TT is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addolink TT is a preferred crosslinker for flexible and rigid foams due to its reactivity and efficiency.
Addolink TT is used in automotive coatings for its excellent adhesion and flexibility.
Addolink TT is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addolink TT is used in water-based polyurethane systems for its compatibility and stability.
Addolink TT is a key component in solvent-based polyurethane coatings.
Addolink TT is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addolink TT is employed in the production of rubber materials for its crosslinking properties.
Addolink TT is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addolink TT is used in the construction industry for high-performance coatings and sealants.

Addolink TT is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addolink TT is a key component in the production of plastics, improving their mechanical properties.
Addolink TT is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addolink TT is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addolink TT is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addolink TT is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addolink TT is used in the production of rubber products, ensuring durable and consistent performance.
Addolink TT is employed in the automotive industry, used in high-performance coatings and adhesives.
Addolink TT is utilized in the production of wood coatings, enhancing their durability and appearance.

Addolink TT is found in the manufacture of specialty coatings for industrial machinery.
Addolink TT is utilized in the formulation of adhesives and sealants.
Addolink TT is a key ingredient in the production of polyurethane elastomers.

Addolink TT is employed in the textile industry to improve the performance of coatings on fabrics.
Addolink TT is used in the rubber industry for its crosslinking properties.
Addolink TT is essential in the production of high-performance industrial coatings.

Addolink TT is a vital component in water-based and solvent-based polyurethane systems.
Addolink TT is applied in the creation of high-performance industrial products.
Addolink TT is used in the formulation of household and industrial coatings.

Addolink TT is utilized in the production of specialty coatings for electronic devices.
Addolink TT is found in the creation of specialty inks for various applications.
Addolink TT is used in the production of ceramic and glass coatings.

Addolink TT is applied in the creation of coatings for plastic surfaces.
Addolink TT is utilized in the formulation of coatings for wood surfaces.
Addolink TT is essential in the production of high-performance adhesives.

Addolink TT is used in the formulation of coatings for automotive applications.
Addolink TT is utilized in the production of specialty adhesives and sealants.
Addolink TT is found in the manufacture of coatings for industrial machinery.

Addolink TT is employed in the creation of specialty coatings for various substrates.
Addolink TT is used in the formulation of high-performance coatings for various applications.
Addolink TT is a key component in the production of specialty inks for flexographic and gravure printing.

Addolink TT is used in the creation of specialty inks for digital printing.
Addolink TT is essential in the production of high-performance industrial products.
Addolink TT is utilized in the manufacture of environmentally friendly industrial products.

Addolink TT is used in the creation of water-based and solvent-based products.
Addolink TT is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addolink TT is a high-performance crosslinker used in polyurethane systems for its excellent reactivity and versatility.
Addolink TT is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addolink TT is a versatile chemical compound used in various polyurethane applications.
Addolink TT is known for its strong crosslinking properties, which improve the durability and performance of polyurethane products.
Addolink TT provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addolink TT is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addolink TT is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addolink TT's non-toxic nature makes it safe for use in various industrial and consumer products.

Addolink TT offers excellent weather resistance, making it suitable for outdoor applications.
Addolink TT is known for its ease of dispersion, ensuring uniform crosslinking in various systems.
Addolink TT is essential in the creation of durable and high-performance polyurethane products.

Addolink TT's strong crosslinking properties make it a preferred choice in the creation of high-quality industrial coatings.
Addolink TT is an important precursor in the production of high-performance adhesives and sealants.
Addolink TT is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addolink TT
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addolink TT is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addolink TT.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addolink TT in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addolink TT at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addolink TT away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addolink TT to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOVATE 3240
Addovate 3240 is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate 3240 is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.
Addovate 3240 is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324

Addovate 3240 is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
Addovate 3240 will result in a deterioration of the compression hardness.
Under-dosage of Addovate 3240 leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.

Addovate 3240 is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.
Addovate 3240 is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate 3240 helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.

This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.
Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.
Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.

Combination with Other Additives: Often used alongside Addovate SM and, if necessary, Addovate LM to prevent core discoloration and maintain the desired foam properties.
Addovate 3240 are added to 100 p.b.w. of polyester polyol.
Over-dosage (> 4.0 p.b.w.) can lead to a decrease in compression hardness, while under-dosage can result in poor homogenization and cell structure damage.

Addovate 3240 is a product of Lanxess, a company specializing in chemical production.
Primarily used in the production of polyester-based flexible slabstock foam.

Addovate 3240 emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.
Addovate 3240 is extensively used in the production of flexible polyester slabstock foam.
This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.

Addovate 3240 plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.
By ensuring a homogeneous mixture, Addovate 3240 helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.
Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.

Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.
Typically available in liquid form for easy mixing and handling.

Dispose of according to local, regional, and national regulations, as detailed in the MSDS.
Essential for ensuring uniform cell structure and consistent physical properties in the foam.
Ensures even distribution of water-insoluble catalysts, crucial for foam quality.

Reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Provides technical support to help customers optimize formulations and resolve processing challenges.
Manufactured under stringent quality control standards to ensure consistent product performance.

Detailed in the Addovate 3240, including potential environmental hazards and safe disposal practices.
Complies with relevant industry standards and regulations, as documented in the MSDS and TDS.
Available through Addovate 3240 and authorized distributors.

This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.

Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate 3240 are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.

Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.
Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.
If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate 3240.

Proper dosage and mixing conditions are critical to achieving the desired foam properties and preventing defects.
Addovate 3240 is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.
Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.

Addovate 3240 is a strong emulsifier & dispersant, prevents cell structure defects.
Addovate 3240 acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
In general 1.0 - 2.0 p.b.w. of Addovate 3240 should be added to 100 p.b.w. polyester polyol.

Addovate 3240 is a non-ionogenic emulsifier.
Over-dosage (> 4.0 p.b.w.) will result in a deterioration of the compression hardness.
Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.

Addovate 3240 has a shelf life of 12 months.
Addovate 3240 is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate 3240 is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox.

Property: Nominal Value
Density at 20 °C: approx. 0.95/g/cm³
Hydroxyl value: approx. 98/mg (KOH)/g
Iodine color :value/max. 10
Flash point: approx. 175/°C
Pour point: approx. - 16/°C
Turbidity point: 55 - 60/%
Viscosity at 20 °C: approx 79/mPa·s
Water content: max. 0.2/%

Addovate 3240 is used for the production of polyester slabstock foam with TDI 65.
Addovate 3240 is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.
The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.

The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.
Addovate 3240's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.
Detailed instructions on safe handling and storage conditions are provided in the MSDS.

Addovate 3240 is important to store Addovate 3240 in a cool, dry place away from direct sunlight and sources of ignition.
When handling Addovate 3240, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.
Disposal of Addovate 3240 should be conducted in accordance with local, regional, and national regulations.

The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.
Addovate 3240 is compatible with polyester polyols, enhancing their processing characteristics.
Addovate 3240 is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.

Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.
Lanxess ensures that Addovate 3240 is manufactured under stringent quality control standards to maintain consistent performance and reliability.

Addovate 3240 provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
Detailed in the technical data sheet, crucial for determining the mixing and processing conditions.
Indicates the level of free acidity in the product, measured in mg KOH/g.

Addovate 3240 helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate 3240 (approx. 0.5 - 1.0 p.b.w.).

Addovate 3240 should be added to 100 p.b.w. polyester polyol.
Addovate 3240 is a non-ionic emulsifier.

Uses:
Addovate 3240 improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.
Enhanced comfort and performance in padded garments and soft furnishings.
Addovate 3240 is predominantly used in the manufacturing of polyester-based flexible slabstock foam.

This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.
Addovate 3240 is used cushions, mattresses, and upholstery.
Addovate 3240 is usedautomotive: Seating, headrests, and interior padding.

Addovate 3240 is used Mattresses, mattress toppers, and pillows.
Addovate 3240 is used Protective foam packaging for delicate items.
Addovate 3240 is used Insulation materials and soundproofing panels.

Addovate 3240 is used Padding for garments and soft furnishings.
Addovate 3240 emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.
Addovate 3240 uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.

Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.
Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.
By ensuring thorough emulsification and dispersion, Addovate 3240 minimizes processing issues and defects, resulting in higher production efficiency.

Reduces waste and the need for rework, making the production process more cost-effective.
Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.
Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.

Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.
Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.
Improves the overall durability and performance of the foam products.

Used in R&D for developing new foam formulations and improving existing ones.
Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.
Addovate 3240 is crucial in producing soft yet durable cushions and upholstery materials that retain their shape and comfort over time.

Used in creating high-quality foam mattresses that offer excellent support and comfort.
Ensures the production of comfortable and resilient car seats and headrests.
Used in various padding applications within vehicle interiors to enhance comfort and safety.

Helps in making products that provide additional comfort and support in bedding.
Produces foam packaging that protects delicate items during shipping and handling, ensuring their safe delivery.
Addovate 3240 is used in producing foam components for items like cushions and pillows.

Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.
Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.

Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.
Reduces material wastage and the need for corrective measures, thereby saving costs and time.

When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.
Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.

Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.
Helps in producing foams that meet environmental standards and regulations.

Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.

Addovate 3240 safety, comfort, and resilience in seating and interior padding.
Protection of sensitive items with cushioning that absorbs shocks and impacts.

Safety Profile
Addovate 3240 exposure to dust, vapors, or mist can cause respiratory irritation, coughing, and difficulty breathing.
Prolonged or high-level exposure may lead to more severe respiratory conditions.
Can cause skin irritation, redness, and dryness.

Prolonged or repeated contact may result in dermatitis or allergic reactions.
Can cause eye irritation, redness, and pain. Severe exposure may result in eye damage.
Addovate 3240 harmful if swallowed.

May cause gastrointestinal irritation, nausea, vomiting, and abdominal pain.
Addovate 3240 may be stable under normal conditions but could become unstable at high temperatures or when in contact with incompatible substances.

Addovate 3240 may react with other chemicals, leading to hazardous reactions such as the release of toxic gases or explosive reactions.
Addovate 3240 may be flammable or combustible under certain conditions.
Addovate 3240 may emit toxic fumes when burned.




ADDOVATE DD 1092
Addovate DD 1092 acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate DD 1092 is an additive for the production of cellular elastomers based on NDI/Polyester technology.
Addovate DD 1092 is a non-ionogenic emulsifier.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1, GK (Oxide), Exolon XW 60, A 1 (Sorbent), PS 1 (Alumina), dialuminum;oxygen(2-), F 360 (Alumina), G 0 (Oxide), G 2 (Oxide), Brockmann, aluminum oxide, Q-Loid A 30, Aluminum oxide (Brockmann).

Addovate DD 1092 is a liquid emulsifier and foam stabilizers used for the production of cellular elastomers based on NDI/polyester technology.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate DD 1092 (approx. 0.5 - 1.0 p.b.w.).
If Addovate DD 1092 is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.

Addovate DD 1092 is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.
Addovate DD 1092 is a liquid emulsifier and retards the foaming reaction.
In general 1.0 - 2.0 p.b.w. of Addovate DD 1092 should be added to 100 p.b.w. polyester polyol.

After a prepolymer has been manufactured on the basis of polyester polyol, NDI and additives (e. g. citric acid, castor oil and Stabaxol),
the reaction is completed by the addition of crosslinker.
Crosslinking is achieved by evenly stirring the crosslinker into the prepolymer which has been cooled to about 90 °C.

To manufacture the crosslinker, Vulkollan 2001 KS is heated to 40 - 50 °C and the specified additives are to be stirred in vigorously.
This mixture must be stored in sealed containers at a temperature of 45 - 50 °C and used within 8 hours.
Addovate DD 1092 is an additive for the production of cellular Vulkollan.

Consult material safety data sheet (MSDS) for additional handling information for Addovate DD 1092.
Addovate DD 1092 is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate DD 1092 helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.

Addovate DD 1092 is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate DD 1092 is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.
Addovate DD 1092 is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.

Specifically, Addovate DD 1092 helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.
This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.
Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.

Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.
Often used alongside Addovate SM and, if necessary, Addovate DD 1092 to prevent core discoloration and maintain the desired foam properties.
Addovate DD 1092 are added to 100 p.b.w. of polyester polyol.

Over-dosage (> 4.0 p.b.w.) can lead to a decrease in compression hardness, while under-dosage can result in poor homogenization and cell structure damage.
Addovate DD 1092 is a product of Lanxess, a company specializing in chemical production.
Primarily used in the production of polyester-based flexible slabstock foam.

Addovate DD 1092 emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.
This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.

Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate DD 1092 are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.

Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.
Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.
If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate DD 1092.

Proper dosage and mixing conditions are critical to achieving the desired foam properties and preventing defects.
Addovate DD 1092 is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.
Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.

For specific inquiries, technical support, or procurement, contacting Lanxess directly or visiting their official website is recommended.
Addovate DD 1092 is extensively used in the production of flexible polyester slabstock foam.
This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.

Addovate DD 1092 plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.
By ensuring a homogeneous mixture, Addovate DD 1092 helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.
Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.

Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.
Typically available in liquid form for easy mixing and handling.
The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.

The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.
Addovate DD 1092's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.
Detailed instructions on safe handling and storage conditions are provided in the MSDS.

Addovate DD 1092 is important to store Addovate DD 1092 in a cool, dry place away from direct sunlight and sources of ignition.
When handling Addovate DD 1092, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.
Disposal of Addovate DD 1092 should be conducted in accordance with local, regional, and national regulations.

The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.
Addovate DD 1092 is compatible with polyester polyols, enhancing their processing characteristics.
Addovate DD 1092 is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.

Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.
Lanxess ensures that Addovate DD 1092 is manufactured under stringent quality control standards to maintain consistent performance and reliability.

Addovate DD 1092 has a shelf life of 4 months.
Addovate DD 1092 is a non-ionic emulsifier.
Addovate DD 1092 is a strong emulsifier & dispersant, prevents cell structure defects.

Addovate DD 1092 retards the foaming reaction.
Addovate DD 1092 will result in a deterioration of the compression hardness.
Addovate DD 1092 is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.

Addovate DD 1092 is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox. 60 mg KOH/g.
Addovate DD 1092 is used for the production of polyester slabstock foam with TDI 65.

Addovate DD 1092 is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
Addovate DD 1092 should be added to 100 p.b.w. polyester polyol.
Over-dosage (> 4.0 p.b.w.) of Addovate DD 1092 will result in a deterioration of the compression hardness.

Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Addovate DD 1092 crosslinking is achieved by evenly stirring the cross-linker into the pre-polymer which has been cooled to about 90°C.

Physical appearance: brownish, viscous liquid
Density (20 °C): approx. 1.04 g/cm³
Viscosity (25 °C): approx. 1 200 mPa.
Initial boiling point: > 200 °C under decomposition
Pour point: < - 10 °C
Flash point: approx. 240 °C
Water content: max. 1.5 %

Addovate DD 1092 is to be stored in a cool and dry place.
When Addovate DD 1092 is stored in firmly closed original containers a shelf-life of 4 months from manufacturing date at pH 7 - 9 can be expected only at temperatures < 6 °C.
Higher storage temperatures reduce the pH-value of Addovate DD 1092.

The contents have to be thoroughly homogenized before use.
The containers should be resealed tightly after use to prevent contamination by impurities and exposure to moisture.
Often used with Addovate SM and Addovate LM to prevent core discoloration and enhance foam quality.

Store in a cool, dry place away from direct sunlight and sources of ignition.
Use gloves, goggles, and protective clothing to prevent skin and eye contact.
Follow the guidelines in the MSDS for safe cleanup and disposal of spills.

Dispose of according to local, regional, and national regulations, as detailed in the MSDS.
Essential for ensuring uniform cell structure and consistent physical properties in the foam.
Ensures even distribution of water-insoluble catalysts, crucial for foam quality.

Reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Provides technical support to help customers optimize formulations and resolve processing challenges.
Manufactured under stringent quality control standards to ensure consistent product performance.

Detailed in the Addovate DD 1092, including potential environmental hazards and safe disposal practices.
Complies with relevant industry standards and regulations, as documented in the MSDS and TDS.
Available through Addovate DD 1092 and authorized distributors.

Uses:
Addovate DD 1092 is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.
Addovate DD 1092 safety, comfort, and resilience in seating and interior padding.
Protection of sensitive items with cushioning that absorbs shocks and impacts.

Addovate DD 1092 improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.
Enhanced comfort and performance in padded garments and soft furnishings.

Addovate DD 1092 is predominantly used in the manufacturing of polyester-based flexible slabstock foam.
This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.
Addovate DD 1092 is used cushions, mattresses, and upholstery.

Addovate DD 1092 is usedautomotive: Seating, headrests, and interior padding.
Addovate DD 1092 is used Mattresses, mattress toppers, and pillows.
Addovate DD 1092 is used Protective foam packaging for delicate items.

Addovate DD 1092 is used Insulation materials and soundproofing panels.
Addovate DD 1092 is used Padding for garments and soft furnishings.
Addovate DD 1092 emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.

Addovate DD 1092 uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.
Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.
Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.

By ensuring thorough emulsification and dispersion, Addovate DD 1092 minimizes processing issues and defects, resulting in higher production efficiency.
Reduces waste and the need for rework, making the production process more cost-effective.
Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.

Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.
Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.
Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.

Improves the overall durability and performance of the foam products.
Used in R&D for developing new foam formulations and improving existing ones.
Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.

Addovate DD 1092 is crucial in producing soft yet durable cushions and upholstery materials that retain their shape and comfort over time.
Used in creating high-quality foam mattresses that offer excellent support and comfort.
Ensures the production of comfortable and resilient car seats and headrests.

Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.
Used in padding for garments, such as jackets and bras, to enhance comfort.

Addovate DD 1092 is used in producing foam components for items like cushions and pillows.
Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.

Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.
Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.

Reduces material wastage and the need for corrective measures, thereby saving costs and time.
When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.

Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.
Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.

Helps in producing foams that meet environmental standards and regulations.
Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.

Safety Profile:
Addovate DD 1092 to accurately determine the hazards of Addovate DD 1092, consulting the product's Safety Data Sheet (SDS) is essential.
The SDS will provide detailed information about the product's potential health, fire, reactivity, and environmental risks.
Exposure to dust, vapors, or mist can cause respiratory irritation.

Prolonged or high-level exposure may lead to more serious respiratory conditions.
Addovate DD 1092 can cause skin irritation, redness, and dryness. Prolonged or repeated contact may result in dermatitis or allergic reactions.
Can cause eye irritation, redness, and pain. Severe exposure may result in damage to the eyes.

ADDOVATE EM
Addovate EM is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.
Addovate EM is used in the low odor polyester flexible slabstock foam for textile application.
Addovate EM acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1.

Addovate EM is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
In general 1.0 - 2.0 p.b.w. of Addovate EM should be added to 100 p.b.w. polyester polyol.
Addovate EM is a non-ionogenic emulsifier.

Addovate EM is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox. 60 mg KOH/g.
Addovate EM is used for the production of polyester slabstock foam with TDI 65.
Addovate EM is a polyether polyol. Acts as an emulsifier for water, catalyst and the polyester polyol.

Improves the open-cell structure of foams.
Addovate EM is used in the low odor polyester flexible slabstock foam for textile application.
Addovate EM is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).

In general 1.0 - 2.0 p.b.w. of Addovate EM should be added to 100 p.b.w. polyester polyol.
Over-dosage (> 4.0 p.b.w.) of Addovate EM will result in a deterioration of the compression hardness.
Under-dosage of Addovate EM leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.

Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate EM (approx. 0.5 - 1.0 p.b.w.).
If Addovate EM is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.
Addovate EM at lower temperatures leads to viscosity increase or solidification of the product at the pour point.

This does not have negative effects on its activity nor is it damaged.
In this case we recommend to store the product at room temperature for 2 weeks or to liquify it for short at max. 50 °C in a heating oven.
The contents have to be thoroughly homogenized before use.

Consult material safety data sheet (MSDS) for additional handling information for Addovate EM.
Addovate EM is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate EM helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.

Addovate EM is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate EM is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.
Addovate EM is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.

Over-dosage (> 4.0 p.b.w.) will result in a deterioration of the compression hardness.
Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Addovate EM is based on a polyether polyol.

Addovate EM improves the open-cell structure of foams.
Addovate EM is an emulsifier for flexible polyurethane slabstock foam for textile applications.
Addovate EM is a non-ionic emulsifier.

Addovate EM helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.
This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.
Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.

Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.
Combination with Other Additives: Often used alongside Addovate SM and, if necessary, Addovate LM to prevent core discoloration and maintain the desired foam properties.
Addovate EM are added to 100 p.b.w. of polyester polyol.

Addovate EM a clear, homogeneous mixture is obtained.
In the production of low odor PUR ester flexible slabstock foam Addovate EM is used as emulsifier in combination with Addovate EM and small amounts of silicone stabilizers.
When mixing with other emulsifiers or additives, it is advisable to carry out laboratory tests for compatibility, as incompatibilities may cause defects in the cellular structure.

Addovate EM is to be stored in a cool and dry place.
When Addovate EM is stored in firmly closed original containers at 10 to 30 °C, a shelf-life of 12 months from manufacturing date can be expected.
The containers should be resealed tightly after use to prevent contamination by impurities and exposure to moisture.

Consult the safety data sheet for relevant safety data & references as well as possibly necessary warning labels.
In the production of PUR ester flexible slabstock foam Addovate EM is used as an emulsifier for water, catalyst(s) (e. g. Addocat 101, Addocat PV, Addocat 117) and the polyester polyol.
Addovate EM also improves the open-cell structure of foams. Addovate EM is usually used in combination with Addovate TX.

The recommended amount is between 1.0 and 4.0 parts by weight Addovate EM to 100 parts by weight polyester polyol.
The following sequence of adding the individual components had proven effective when manufacturing the activator batch: water, catalyst(s), Addovate EM, Addovate TX. A clear, homogeneous mixture is obtained.
In the production of low odor PUR ester flexible slabstock foam Addovate EM is used as emulsifier / stabilizer in combination with Addovate 3240 and small amounts of silicone stabilizers.

Guide formulations may be provided upon request.
Addovate EM is to be stored in a cool and dry place.
When Addovate EM is stored in firmly closed original containers at 10 to 30 °C, a shelf-life of 12 months from manufacturing date can be expected.

The containers should be resealed tightly after use to prevent contamination by impurities and exposure to moisture.
Relevant safety data and references as well as possibly necessary warning labels are to be found in safety data sheet.
Addovate EM is a strong emulsifier & dispersant, prevents cell structure defects.

Acid value: 4 - 6 mg (KOH)/g
Density at 20 °C approx: 1.0 g/cm³
Flash point approx: 185 °C
Hydroxyl value: 49 - 55 mg (KOH)/g
Pour point approx: - 23 °C
Viscosity at 25 °C: 85 - 120 mPa·s
Water content max: 0.5 %

Addovate EM is a non-ionic emulsifier for the production of PUR ester flexible slabstock foam.
Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.
Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.

If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate EM.
Proper dosage and mixing conditions are critical to achieving the desired foam properties and preventing defects.
Addovate EM is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.

Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.
For specific inquiries, technical support, or procurement, contacting Lanxess directly or visiting their official website is recommended.
Addovate EM is extensively used in the production of flexible polyester slabstock foam.

This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.
Addovate EM plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.
By ensuring a homogeneous mixture, Addovate EM helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.

Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.
Typically available in liquid form for easy mixing and handling.

The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.
The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.
Addovate EM's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.

Detailed instructions on safe handling and storage conditions are provided in the MSDS.
Addovate EM is important to store Addovate EM in a cool, dry place away from direct sunlight and sources of ignition.
When handling Addovate EM, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.

Disposal of Addovate EM should be conducted in accordance with local, regional, and national regulations.
The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.
Addovate EM is compatible with polyester polyols, enhancing their processing characteristics.

Addovate EM is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.
Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.

Lanxess ensures that Addovate EM is manufactured under stringent quality control standards to maintain consistent performance and reliability.
Addovate EM provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
The recommended amount is between 1.0 and 4.0 parts by weight Addovate EM to 100 parts by weight polyester polyol.

The following sequence of adding the individual components had proven effective when manufacturing the activator batch: water, catalyst(s), Addovate EM, Addovate TX. A clear, homogeneous mixture is obtained.
Addovate EM is a polyether polyol.
Addovate EM acts as an emulsifier for water, catalyst and the polyester polyol.

When Addovate EM is stored in firmly closed original containers at 10 to 30 °C, a shelf-life of 12 months from manufacturing date can be expected.
The containers should be resealed tightly after use to prevent contamination by impurities and exposure to moisture.
Consult the safety data sheet for relevant safety data & references as well as possibly necessary warning labels.

PUR ester flexible slabstock foam for "textile" applications:
In the production of PUR ester flexible slabstock foam Addovate EM is used as an emulsifier for water, catalyst(s) (e. g. Addocat 101, Addocat PV, Addocat 117) and the polyester polyol.
Addovate EM also improves the open-cell structure of foams. Addovate EM is usually used in combination with Addovate TX.

Addovate EM emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.
This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.

Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate EM are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.

Uses:
Addovate EM is used cushions, mattresses, and upholstery.
Addovate EM is usedautomotive: Seating, headrests, and interior padding.
Addovate EM is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.

Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.
Used in padding for garments, such as jackets and bras, to enhance comfort.
Addovate EM is used in producing foam components for items like cushions and pillows.

Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.
Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.

Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.
Addovate EM is used Insulation materials and soundproofing panels.

Addovate EM is used Padding for garments and soft furnishings.
Addovate EM emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.

Addovate EM uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.
Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.
Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.

By ensuring thorough emulsification and dispersion, Addovate EM minimizes processing issues and defects, resulting in higher production efficiency.
Reduces waste and the need for rework, making the production process more cost-effective.
Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.

Addovate EM safety, comfort, and resilience in seating and interior padding.
Protection of sensitive items with cushioning that absorbs shocks and impacts.
Addovate EM improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.

Enhanced comfort and performance in padded garments and soft furnishings.
Addovate EM is predominantly used in the manufacturing of polyester-based flexible slabstock foam.
Reduces material wastage and the need for corrective measures, thereby saving costs and time.

When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.

Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.
Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.

Helps in producing foams that meet environmental standards and regulations.
Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.

Safety Profile:
To understand the specific hazards associated with Addovate EM, it's essential to refer to its Safety Data Sheet (SDS).
However, without access to the SDS, I can provide a general overview of potential hazards based on common types of chemical additives similar to Addovate EM.
Inhalation of dust, vapors, or mist can cause respiratory irritation or more severe effects such as difficulty breathing.

Addovate EM can cause skin irritation, dryness, or allergic reactions. Prolonged contact may result in dermatitis.
Can cause eye irritation, redness, and possible damage to the eyes.
Addovate EM harmful if swallowed, leading to digestive system irritation or more severe internal effects.


ADDOVATE SM OPTIMIZED
Addovate SM optimized is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.
Addovate SM optimized emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.
Addovate SM optimized is extensively used in the production of flexible polyester slabstock foam.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1, GK (Oxide), Exolon XW 60, A 1 (Sorbent), PS 1 (Alumina), dialuminum;oxygen(2-), F 360 (Alumina), G 0 (Oxide), G 2 (Oxide), Brockmann, aluminum oxide, Q-Loid A 30, Aluminum oxide (Brockmann), KHP 2.

Addovate SM optimized is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate SM optimized helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.

Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate SM optimized are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.

Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.
Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate SM optimized (approx. 0.5 - 1.0 p.b.w.).

Storage Addovate SM optimized at lower temperatures leads to viscosity increase or solidification of the product at the pour point.
This does not have negative effects on its activity nor is it damaged.
In this case we recommend to store the product at room temperature for 2 weeks or to liquify it for short at max. 50 °C in a heating oven.

The contents have to be thoroughly homogenized before use.
Consult material safety data sheet (MSDS) for additional handling information for Addovate SM optimized.
This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.

Addovate SM optimized is used for the production of polyester slabstock foam with TDI 65.
Addovate SM optimized is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
In general 1.0 - 2.0 p.b.w. of Addovate SM optimized should be added to 100 p.b.w. polyester polyol.

Over-dosage (> 4.0 p.b.w.) of Addovate SM optimized will result in a deterioration of the compression hardness.
In general 1.0 - 2.0 p.b.w. of Addovate SM optimized should be added to 100 p.b.w. polyester polyol.
Proper dosage and mixing conditions are critical to achieving the desired foam properties and preventing defects.

Addovate SM optimized is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.
Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.
For specific inquiries, technical support, or procurement, contacting Lanxess directly or visiting their official website is recommended.

This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.
Addovate SM optimized plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.

By ensuring a homogeneous mixture, Addovate SM optimized helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.
Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.

Typically available in liquid form for easy mixing and handling.
The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.
The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.

Addovate SM optimized's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.
Often used with Addovate SM and Addovate LM to prevent core discoloration and enhance foam quality.

Addovate SM optimized is a non-ionogenic emulsifier.
Over-dosage (> 4.0 p.b.w.) will result in a deterioration of the compression hardness.
Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.

Addovate SM optimized has a shelf life of 12 months.
Addovate SM optimized is a strong emulsifier & dispersant, prevents cell structure defects.
Addovate SM optimized is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.

Detailed instructions on safe handling and storage conditions are provided in the MSDS.
Addovate SM optimized is important to store Addovate SM optimized in a cool, dry place away from direct sunlight and sources of ignition.
When handling Addovate SM optimized, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.

Disposal of Addovate SM optimized should be conducted in accordance with local, regional, and national regulations.
The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.

Addovate SM optimized is compatible with polyester polyols, enhancing their processing characteristics.
Addovate SM optimized is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.

Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.
Lanxess ensures that Addovate SM optimized is manufactured under stringent quality control standards to maintain consistent performance and reliability.

Physical appearance: yellowish liquid
Acid value: 9 - 11 mg (KOH)/g
Amine value: 9 - 12 mg (KOH)/g
Appearance: yellowish liquid
Density at 20 °C: approx. 1.04 g/cm3
Viscosity at 25 °C: 300 - 600 mPa·s
Flash point: > 100 °C
Pour point: < - 3 °C
Solubility: in water unlimited
Sulfation degree: 32 - 36 %
Water content: 49 - 51 %

Addovate SM optimized provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
Detailed in the technical data sheet, crucial for determining the mixing and processing conditions.
Indicates the level of free acidity in the product, measured in mg KOH/g.

If Addovate SM optimized is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.
If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate SM optimized.
Addovate SM optimized is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.

Specifically, Addovate SM optimized helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.
Addovate SM optimized acts as a dispersant and emulsifier for the production of polyester based.
Addovate SM optimized is a non-ionic emulsifier.

This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.
Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.
Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.

Combination with Other Additives: Often used alongside Addovate SM and, if necessary, Addovate LM to prevent core discoloration and maintain the desired foam properties.
Addovate SM optimized are added to 100 p.b.w. of polyester polyol.
Over-dosage (> 4.0 p.b.w.) can lead to a decrease in compression hardness, while under-dosage can result in poor homogenization and cell structure damage.

Addovate SM optimized is a product of Lanxess, a company specializing in chemical production.
Primarily used in the production of polyester-based flexible slabstock foam.
Under-dosage of Addovate SM optimized leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.

Addovate SM optimized is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate SM optimized is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate SM optimized is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox.

Uses:
Addovate SM optimized is used cushions, mattresses, and upholstery.
Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.
Achieves uniformity in critical properties such as density, compression set, and rebound resilience.

Contributes to the production of durable foam products that withstand prolonged use without significant degradation.
Helps in producing foams that meet environmental standards and regulations.
Ensures that foam products comply with safety standards for use in consumer and industrial applications.

Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.
Addovate SM optimized safety, comfort, and resilience in seating and interior padding.
Protection of sensitive items with cushioning that absorbs shocks and impacts.

Addovate SM optimized improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.
Enhanced comfort and performance in padded garments and soft furnishings.
Addovate SM optimized is predominantly used in the manufacturing of polyester-based flexible slabstock foam.

Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.
Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.
Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.

Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.
Improves the overall durability and performance of the foam products.

Used in R&D for developing new foam formulations and improving existing ones.
Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.

This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.
Addovate SM optimized is usedautomotive: Seating, headrests, and interior padding.
Addovate SM optimized is used Mattresses, mattress toppers, and pillows.

Addovate SM optimized is used Protective foam packaging for delicate items.
Addovate SM optimized is used Insulation materials and soundproofing panels.
Addovate SM optimized is used Padding for garments and soft furnishings.

Addovate SM optimized is crucial in producing soft yet durable cushions and upholstery materials that retain their shape and comfort over time.
Used in creating high-quality foam mattresses that offer excellent support and comfort.
Ensures the production of comfortable and resilient car seats and headrests.

Used in various padding applications within vehicle interiors to enhance comfort and safety.
Helps in making products that provide additional comfort and support in bedding.
Produces foam packaging that protects delicate items during shipping and handling, ensuring their safe delivery.

Addovate SM optimized is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.
Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.
Used in padding for garments, such as jackets and bras, to enhance comfort.

Addovate SM optimized is used in producing foam components for items like cushions and pillows.
Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.

Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.
Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.

Reduces material wastage and the need for corrective measures, thereby saving costs and time.
When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.

Safety Profile:
Addovate SM optimized is a chemical product, and understanding its hazards is crucial for safe handling and usage.
The hazards can typically be found in its Safety Data Sheet (SDS), which provides detailed information about the substance's potential health, fire, reactivity, and environmental risks.
Can cause respiratory irritation or more severe effects if inhaled in large quantities.

Addovate SM optimized may cause skin irritation, dryness, or allergic reactions.
Can cause eye irritation, redness, or damage.
Harmful if swallowed, leading to digestive system irritation or more serious internal effects.


ADDOVATE SV
Addovate SV is important to store Addovate SV in a cool, dry place away from direct sunlight and sources of ignition.
Addovate SV, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.
Addovate SV's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1, GK (Oxide), Exolon XW 60, A 1 (Sorbent), PS 1 (Alumina), dialuminum;oxygen(2-), F 360 (Alumina), G 0 (Oxide), G 2 (Oxide), Brockmann, aluminum oxide, Q-Loid A 30, Aluminum oxide (Brockmann), KHP 2, RC 172DBM, Aluminum oxide (fibrous forms), CCRIS 6605, HSDB 506, LA 6, Aluminium lake, Aluminum oxide (2:3), Aluminum oxide (ignited), Aluminum oxide (brockmann) (form), Aluminum oxide G, EINECS 215-691-6, KA 101, UNII-LMI26O6933, Aluminum (II) oxide, AI3-02904, LMI26O6933, Aluminum oxide, anhydrous, BETA-ALUMINIUM OXIDE, A1-3438 T 1/8'', GAMMA-ALUMINIUM OXIDE, A1-0104 T 3/16'', A1-1404 T 3/16'', A1-3945 E 1/16'', A1-3980 T 5/32'', A1-4028 T 3/16'', A1-4126 E 1/16'', EC 215-691-6, 12522-88-2, 12737-16-5, Alumina Ceramic, Aluminum oxide, mesoporous, Aluminum trioxide, Hypalox II, Dialuminum trioxide, Aluminum oxide (Al2O3), Aluminum sesquioxide, Aluminum oxide, single crystal, ALUMINIUM OXIDE (MART.), ALUMINIUM OXIDE [MART.], Oxide, Aluminum, beta-Aluminum oxide, Aluminum oxide [NF], ALUMINUM OXIDE, ANHYDROUS (EP IMPURITY), ALUMINUM OXIDE, ANHYDROUS [EP IMPURITY], A1-1401 P(MS), aluminiumoxid.

Addovate SV is an aqueous solution of fatty acid sulfonate.
Acts as an emulsifier and crosslinker for the production of cellular Vulkollan.
Often used with Addovate SV and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.

If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate SV.
Proper dosage and mixing conditions are critical to achieving the desired foam properties and preventing defects.
Addovate SV is extensively used in the production of flexible polyester slabstock foam.

This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.
Addovate SV plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.
By ensuring a homogeneous mixture, Addovate SV helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.

Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.
Typically available in liquid form for easy mixing and handling.

The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.
The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.
Detailed instructions on safe handling and storage conditions are provided in the MSDS.

Disposal of Addovate SV should be conducted in accordance with local, regional, and national regulations.
The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.
Addovate SV is compatible with polyester polyols, enhancing their processing characteristics.

Addovate SV is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.
Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.

Lanxess ensures that Addovate SV is manufactured under stringent quality control standards to maintain consistent performance and reliability.
Addovate SV provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
Detailed in the technical data sheet, crucial for determining the mixing and processing conditions.

Indicates the level of free acidity in the product, measured in mg KOH/g.
Determined according to DIN ISO 2592 standards
Specified under recommended storage conditions

Add 1.0 - 2.0 parts by weight (p.b.w.) of Addovate SV to 100 p.b.w. of polyester polyol.
Addovate SV can lead to reduced compression hardness.
Results in poor catalyst homogenization and potential cell structure damage.

Often used with Addovate SM and Addovate LM to prevent core discoloration and enhance foam quality.
Store in a cool, dry place away from direct sunlight and sources of ignition.
Addovate SV use gloves, goggles, and protective clothing to prevent skin and eye contact.

Follow the guidelines in the MSDS for safe cleanup and disposal of spills.
Dispose of according to local, regional, and national regulations, as detailed in the MSDS.

Essential for ensuring uniform cell structure and consistent physical properties in the foam.
Ensures even distribution of water-insoluble catalysts, crucial for foam quality.
Reduces processing issues and defects, leading to higher production efficiency and reduced waste.

Addovate SV provides technical support to help customers optimize formulations and resolve processing challenges.
Manufactured under stringent quality control standards to ensure consistent product performance.
Detailed in the Addovate SV, including potential environmental hazards and safe disposal practices.

Complies with relevant industry standards and regulations, as documented in the MSDS and TDS.
Available through Addovate SV and authorized distributors.
If Addovate SV is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.

Shelf life: 12 months in originally closed, moisture-tight containers.
Storage temperature: + 10 °C to + 30 °C (optimum).

Storage Addovate SV at lower temperatures leads to viscosity increase or solidification of the product at the pour point.
This does not have negative effects on its activity nor is it damaged.
In this case we recommend to store the product at room temperature for 2 weeks or to liquify it for short at max. 50 °C in a heating oven.

The contents have to be thoroughly homogenized before use.
Consult material safety data sheet (MSDS) for additional handling information for Addovate SV.
Addovate SV is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.

The water component serves to promote the propellant effects.
Addovate SV acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
To improve dispensing characteristics, a crosslinker should be manufactured containing Addovate SV.

Parts by weight of the Addovate SV also used for the prepolymer. The shelf life is 6 months.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate SV (approx. 0.5 - 1.0 p.b.w.).
This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.

Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.
Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Addovate SV is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.

Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.
For specific inquiries, technical support, or procurement, contacting Lanxess directly or visiting their official website is recommended.

Addovate SV leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Addovate SV emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.

Property: Nominal / Value Unit
Acid value:16 - 20 / mg (KOH)/g
Density at 20 °C: 1.04 - 1.06 / g/cm³
Flash point: > 100 / °C
Pour point: < -7 / °C
Viscosity at 20 °C: 150 - 300 7 mPa·s
Water content: 49 - 51 / %

Addovate SV helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.
Addovate SV is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate SV is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.

Addovate SV is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
In general 1.0 - 2.0 p.b.w. of Addovate SV should be added to 100 p.b.w. polyester polyol.
Addovate SV is a non-ionogenic emulsifier.

Over-dosage (> 4.0 p.b.w.) will result in a deterioration of the compression hardness.
Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Addovate SV has a shelf life of 12 months.

Addovate SV is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate SV is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox. 60 mg KOH/g.
Addovate SV is a non-ionic emulsifier.

Addovate SV is a strong emulsifier & dispersant, prevents cell structure defects.
Addovate SV is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.
Addovate SV is used for the production of polyester slabstock foam with TDI 65.

Addovate SV is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
In general 1.0 - 2.0 p.b.w. of Addovate SV should be added to 100 p.b.w. polyester polyol.
Over-dosage (> 4.0 p.b.w.) of Addovate SV will result in a deterioration of the compression hardness.

Uses:
Used in creating high-quality foam mattresses that offer excellent support and comfort.
Ensures the production of comfortable and resilient car seats and headrests.
Used in various padding applications within vehicle interiors to enhance comfort and safety.

Helps in making products that provide additional comfort and support in bedding.
Produces foam packaging that protects delicate items during shipping and handling, ensuring their safe delivery.
Addovate SV is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.

Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.
Used in padding for garments, such as jackets and bras, to enhance comfort.
Addovate SV is used in producing foam components for items like cushions and pillows.

Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.
Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.

Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.
Reduces material wastage and the need for corrective measures, thereby saving costs and time.

When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.
Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.

Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.
Helps in producing foams that meet environmental standards and regulations.

Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.
Addovate SV safety, comfort, and resilience in seating and interior padding.

Protection of sensitive items with cushioning that absorbs shocks and impacts.
Addovate SV improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.
Enhanced comfort and performance in padded garments and soft furnishings.

Addovate SV is predominantly used in the manufacturing of polyester-based flexible slabstock foam.
This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.
Addovate SV is used cushions, mattresses, and upholstery.

Addovate SV is usedautomotive: Seating, headrests, and interior padding.
Addovate SV is used Mattresses, mattress toppers, and pillows.
Addovate SV is used Protective foam packaging for delicate items.

Addovate SV is used Insulation materials and soundproofing panels.
Addovate SV is used Padding for garments and soft furnishings.
Addovate SV emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.

Addovate SV uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.
Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.
Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.

By ensuring thorough emulsification and dispersion, Addovate SV minimizes processing issues and defects, resulting in higher production efficiency.
Reduces waste and the need for rework, making the production process more cost-effective.
Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.

Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.
Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.
Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.

Improves the overall durability and performance of the foam products.
Used in R&D for developing new foam formulations and improving existing ones.
Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.

Safety Profile:
This might include respiratory irritants or sensitizers.
Prolonged or repeated exposure to certain additives might cause skin or eye irritation, respiratory issues, or other health effects.

If not managed properly, disposal of polymer-based products can lead to environmental contamination.
Some polymer additives can release hazardous chemicals during processing or application.

ADDOVATE TX
Addovate TX is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.
Addovate TX has to be thoroughly homogenized by rolling or tumbling the drums or stirring the contents.
Addovate TX is usually used in combination with Addovate EM in the manufacture of polyester slabstock foam. With a combination of Addovate TX, good foaming control resulting in fine cell structure can be achieved.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1, GK (Oxide), Exolon XW 60, A 1 (Sorbent), PS 1 (Alumina), dialuminum;oxygen(2-), F 360 (Alumina), G 0 (Oxide), G 2 (Oxide), Brockmann, aluminum oxide, Q-Loid A 30, Aluminum oxide (Brockmann), KHP 2, RC 172DBM, Aluminum oxide (fibrous forms), CCRIS 6605, HSDB 506, LA 6, Aluminium lake, Aluminum oxide (2:3), Aluminum oxide (ignited), Aluminum oxide (brockmann) (form), Aluminum oxide G, EINECS 215-691-6, KA 101, UNII-LMI26O6933, Aluminum (II) oxide, AI3-02904, LMI26O6933, Aluminum oxide, anhydrous, BETA-ALUMINIUM OXIDE, A1-3438 T 1/8'', GAMMA-ALUMINIUM OXIDE, A1-0104 T 3/16'', A1-1404 T 3/16'', A1-3945 E 1/16'', A1-3980 T 5/32'', A1-4028 T 3/16'', A1-4126 E 1/16'', EC 215-691-6, 12522-88-2, 12737-16-5, Alumina Ceramic, Aluminum oxide, mesoporous, Aluminum trioxide, Hypalox II, Dialuminum trioxide, Aluminum oxide (Al2O3), Aluminum sesquioxide, Aluminum oxide, single crystal, ALUMINIUM OXIDE (MART.), ALUMINIUM OXIDE [MART.], Oxide, Aluminum, beta-Aluminum oxide, Aluminum oxide [NF], ALUMINUM OXIDE, ANHYDROUS (EP IMPURITY), ALUMINUM OXIDE, ANHYDROUS [EP IMPURITY], A1-1401 P(MS), aluminiumoxid.

Addovate TX provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
Detailed in the technical data sheet, crucial for determining the mixing and processing conditions.
Indicates the level of free acidity in the product, measured in mg KOH/g.

The proportions which should be used are 1.0-3.0 p.b.w.
Addovate TX to 100.0 p.b.w. polyester polyol.
Addovate TX is a strong emulsifier & dispersant, prevents cell structure defects.

The specific density and viscosity values are provided in Addovate TX's technical data sheet (TDS), which can be used to determine the optimal processing conditions.
The acid value, measured in mg KOH/g, indicates the amount of free acidity in Addovate TX, which is crucial for understanding its reactivity and compatibility with other components.
When handling Addovate TX, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.

Addovate TX has a shelf life of 6 months.
Addovate TX is a non-ionic emulsifier.
The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.

Addovate TX is compatible with polyester polyols, enhancing their processing characteristics.
Detailed instructions on safe handling and storage conditions are provided in the MSDS.
Addovate TX is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.

Addovate TX is a product of Lanxess, a company specializing in chemical production.
Primarily used in the production of polyester-based flexible slabstock foam.
Addovate TX emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.

This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.
Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.

Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate TX are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.
Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.

Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.
If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate TX.
Accurate measurement and mixing are crucial for optimal performance.

The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.
Lanxess ensures that Addovate TX is manufactured under stringent quality control standards to maintain consistent performance and reliability.

The following sequence for adding the individual components has proven effective in the manufacture of catalyst compounds: water, catalyst, Addovate EM, Addovate TX.
A clear, homogeneous mixture is produced.
Addovate TX Plastic Additives Business offers products for all kinds of plastics solutions.

The high-quality Addovate TX and finishing chemicals in the Plastic Addovate TX Business Line improve the processability of ingredients and especially the properties of end products.
Addovate TX acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate TX is a non-ionogenic emulsifier.

Over-dosage (> 4.0 p.b.w.) will result in a deterioration of the compression hardness.
Under-dosage of leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Addovate TX has a shelf life of 12 months.

Addovate TX is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate TX is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox. 60 mg KOH/g.
Addovate TX is used for the production of polyester slabstock foam with TDI 65.

Addovate TX is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
In general 1.0 - 2.0 p.b.w. of Addovate TX should be added to 100 p.b.w. polyester polyol.
Over-dosage (> 4.0 p.b.w.) of Addovate TX will result in a deterioration of the compression hardness.

Under-dosage of Addovate TX leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate TX (approx. 0.5 - 1.0 p.b.w.).
If Addovate TX is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.

Shelf life: 12 months in originally closed, moisture-tight containers.
Storage temperature: + 10 °C to + 30 °C (optimum).
Storage Addovate TX at lower temperatures leads to viscosity increase or solidification of the product at the pour point.

This does not have negative effects on its activity nor is it damaged.
In this case we recommend to store the product at room temperature for 2 weeks or to liquify it for short at max. 50 °C in a heating oven.
The contents have to be thoroughly homogenized before use.

Consult material safety data sheet (MSDS) for additional handling information for Addovate TX.
Addovate TX is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate TX helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.

Addovate TX is typically used in combination with Addovate SM and, if necessary, Addovate LM.
Addovate TX is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.

Chemical composition: Preparation of sulphonated hydrocarbons
Physical appearance: brown liquid
Density (20 °C): approx. 0.99 g/cm³
Initial boiling point: approx. > 100 °C
Pour point: approx. - 5 °C
Flash point: > 100 °C
(ASTM-D 93, DIN EN 22719)
Miscibility with water: dispersible
Acid number: 7.0 ± 1.0 mg KOH/g
Water content: max. 1.0 %
Viscosity (25 °C): 350 ± 100 mPa.s

Addovate TX is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Specifically, Addovate TX helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.
This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.

Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.
Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.
Combination with Other Additives: Often used alongside Addovate SM and, if necessary, Addovate LM to prevent core discoloration and maintain the desired foam properties.

Addovate TX are added to 100 p.b.w. of polyester polyol.
Addovate TX plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.
By ensuring a homogeneous mixture, Addovate TX helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.

Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.
Addovate TX typically available in liquid form for easy mixing and handling.

Addovate TX's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.
Addovate TX is a prepation of sulphonated hydrocarbons. Acts as an emulsifier/stabilizer for the production of polyurethane polyester flexible slabstock foam.
Before processing, ithas to be thoroughly homogenized by rolling or tumbling the drums or stirring the contents.

With a combination of Addovate TX, good foaming control resulting in fine cell structure can be achieved.
Addovate TX is important to store Addovate TX in a cool, dry place away from direct sunlight and sources of ignition.
Addovate TX should be conducted in accordance with local, regional, and national regulations.

Uses:
When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
By ensuring thorough emulsification and dispersion, Addovate TX minimizes processing issues and defects, resulting in higher production efficiency.
Reduces waste and the need for rework, making the production process more cost-effective.

Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.
Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.
Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.

Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.
Improves the overall durability and performance of the foam products.
Used in R&D for developing new foam formulations and improving existing ones.

Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.
Addovate TX is crucial in producing soft yet durable cushions and upholstery materials that retain their shape and comfort over time.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.

Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.
Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.

Helps in producing foams that meet environmental standards and regulations.
Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.

Addovate TX safety, comfort, and resilience in seating and interior padding.
Protection of sensitive items with cushioning that absorbs shocks and impacts.
Addovate TX improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.

Enhanced comfort and performance in padded garments and soft furnishings.
Addovate TX is predominantly used in the manufacturing of polyester-based flexible slabstock foam.
This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.

Addovate TX is used cushions, mattresses, and upholstery.
Addovate TX is usedautomotive: Seating, headrests, and interior padding.

Addovate TX is used Mattresses, mattress toppers, and pillows.
Addovate TX is used Protective foam packaging for delicate items.

Addovate TX is used Insulation materials and soundproofing panels.
Addovate TX is used Padding for garments and soft furnishings.
Addovate TX emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.

Addovate TX uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.
Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.
Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.

Used in creating high-quality foam mattresses that offer excellent support and comfort.
Ensures the production of comfortable and resilient car seats and headrests.
Used in various padding applications within vehicle interiors to enhance comfort and safety.

Helps in making products that provide additional comfort and support in bedding.
Produces foam packaging that protects delicate items during shipping and handling, ensuring their safe delivery.
Addovate TX is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.

Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.
Used in padding for garments, such as jackets and bras, to enhance comfort.
Addovate TX is used in producing foam components for items like cushions and pillows.

Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.
Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.
Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.

Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.
Reduces material wastage and the need for corrective measures, thereby saving costs and time.

Safety Profile:
Some polymer additives can release hazardous chemicals during processing or application.
This might include respiratory irritants or sensitizers.
Fire and Explosion: Depending on the chemical makeup, some additives can be flammable or pose a fire risk under certain conditions.

Prolonged or repeated exposure to certain additives might cause skin or eye irritation, respiratory issues, or other health effects.
If not managed properly, disposal of polymer-based products can lead to environmental contamination.

ADDOVATE WM
Addovate WM is a non-ionic dispersant or emulsifier for the production of PUR ester flexible slab-stock foam.
Addovate WM is used in combination with Addovate SM.
Addovate WM is designed to homogeneously disperse water, water-insoluble catalysts and paraffin oil in the activator batch and to aid the mixing of reaction components in the mixing chamber.

CAS Number: 1344-28-1
EINECS Number: 215-691-6

Synonyms: Abramant, Compalox, Faserton, Martoxin, Poraminar, Abramax, Abrasit, Almite, Aloxite, Alundum, Conopal, Diadur, Lucalox, Saffie, delta alumina, Dural, Aluminum lake, Dispal alumina, Theta alumina, Eta-alumina, Catapal S, Jubenon R, Microgrit WCA, Neobead C, Alumite (oxide), Dispal M, Ketjen B, Cab-O-grip, Fiber FP, Ludox CL, Aluminite 37, Alon C, Catapal SB alumina, Alundum 600, Dotment 324, Dotment 358, Alcoa F 1, GK (Oxide), Exolon XW 60, A 1 (Sorbent), PS 1 (Alumina), dialuminum;oxygen(2-), F 360 (Alumina), G 0 (Oxide), G 2 (Oxide), Brockmann, aluminum oxide, Q-Loid A 30, Aluminum oxide (Brockmann), KHP 2, RC 172DBM, Aluminum oxide (fibrous forms), CCRIS 6605, HSDB 506, LA 6, Aluminium lake, Aluminum oxide (2:3), Aluminum oxide (ignited), Aluminum oxide (brockmann) (form), Aluminum oxide G, EINECS 215-691-6, KA 101, UNII-LMI26O6933, Aluminum (II) oxide, AI3-02904, LMI26O6933, Aluminum oxide, anhydrous, BETA-ALUMINIUM OXIDE, A1-3438 T 1/8'', GAMMA-ALUMINIUM OXIDE, A1-0104 T 3/16'', A1-1404 T 3/16'', A1-3945 E 1/16'', A1-3980 T 5/32'', A1-4028 T 3/16'', A1-4126 E 1/16'', EC 215-691-6, 12522-88-2, 12737-16-5, Alumina Ceramic, Aluminum oxide, mesoporous, Aluminum trioxide, Hypalox II, Dialuminum trioxide, Aluminum oxide (Al2O3), Aluminum sesquioxide, Aluminum oxide, single crystal, ALUMINIUM OXIDE (MART.), ALUMINIUM OXIDE [MART.], Oxide, Aluminum, beta-Aluminum oxide, Aluminum oxide [NF], ALUMINUM OXIDE, ANHYDROUS (EP IMPURITY), ALUMINUM OXIDE, ANHYDROUS [EP IMPURITY], A1-1401 P(MS), aluminiumoxid.

Addovate WM is a non-ionic emulsifier.
Addovate WM acts as a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Recommended dosage level is 1-2 parts by weight to 100 parts by weight polyester polyol.

In general 1.0 - 2.0 p.b.w. of Addovate WM should be added to 100 p.b.w. polyester polyol.
Addovate WM is a non-ionogenic emulsifier.
Addovate WM is a strong emulsifier & dispersant, prevents cell structure defects.

Addovate WM is a dispersant and emulsifier for the production of polyester based flexible slabstock foam.
Addovate WM is an emulsifier for water, paraffin oil and water-insoluble catalysts (e.g. Addocat DB) in polyester-polyols with OH-value ofapprox.
Addovate WM is used for the production of polyester slabstock foam with TDI 65.

Addovate WM is used in combination with Addovate SM and if necessary Addovate LM (prevents core discolouration).
In general 1.0 - 2.0 p.b.w. of Addovate WM should be added to 100 p.b.w. polyester polyol.
Over-dosage (> 4.0 p.b.w.) of Addovate WM will result in a deterioration of the compression hardness.

Under-dosage of Addovate WM leads to a badly homogenized catalyst mixture which results in severe damages to the cell structure.
Should a silicone stabilizer be processed which emulsifies Addocat DB not sufficiently, it is recommended to add a sufficient amount of Addovate WM (approx. 0.5 - 1.0 p.b.w.).
If Addovate WM is used in combination with any other emulsifier or additive, it is advisable to test in respect of compatibility in the lab prior to processing, otherwise incompatibility may result in damages to the cell structure.

Shelf life: 12 months in originally closed, moisture-tight containers.
Storage temperature: + 10 °C to + 30 °C (optimum).
Storage Addovate WM at lower temperatures leads to viscosity increase or solidification of the product at the pour point.

This does not have negative effects on its activity nor is it damaged.
In this case we recommend to store the product at room temperature for 2 weeks or to liquify it for short at max. 50 °C in a heating oven.
The contents have to be thoroughly homogenized before use.

Consult material safety data sheet (MSDS) for additional handling information for Addovate WM.
Addovate WM is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate WM helps to disperse water, paraffin oil, and water-insoluble catalysts within polyester polyols.

Addovate WM is produced by Lanxess, a global specialty chemicals company that provides a wide range of chemical products for various industries.
Detailed technical data sheets (TDS) and material safety data sheets (MSDS) are available from Lanxess, providing comprehensive information on the product's properties, handling, and safety.
For specific inquiries, technical support, or procurement, contacting Lanxess directly or visiting their official website is recommended.

Addovate WM is extensively used in the production of flexible polyester slabstock foam.
This type of foam is commonly used in various applications such as furniture, mattresses, automotive seating, and packaging materials.
Addovate WM plays a critical role in emulsifying water-insoluble catalysts like Addocat DB, ensuring these catalysts are evenly distributed within the foam matrix.

By ensuring a homogeneous mixture, Addovate WM helps in producing foam with uniform cell structure, which translates to consistent physical properties throughout the foam.
Proper emulsification of components reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Compatible with various polyester polyols and can be adjusted in combination with other additives to meet specific processing and product requirements.

Typically available in liquid form for easy mixing and handling.
The specific density and viscosity values are provided in the product's technical data sheet (TDS), which can be used to determine the optimal processing conditions.
The acid value, measured in mg KOH/g, indicates the amount of free acidity in the product, which is crucial for understanding its reactivity and compatibility with other components.

Addovate WM's shelf life under specified storage conditions is provided in the MSDS, ensuring users can plan their inventory and usage accordingly.
Detailed instructions on safe handling and storage conditions are provided in the MSDS.
Addovate WM is typically used in combination with Addovate SM and, if necessary, Addovate LM.

Addovate WM is used to improve the mixing and homogenization of reaction components in foam production, ensuring a uniform cell structure and preventing defects​.
Addovate WM is a non-ionic dispersant and emulsifier used in the production of polyester-based flexible slabstock foam.
Addovate WM is a non-ionic emulsifier for water, paraffin oil, and water insoluble catalysts in polyester polyols for the production of flexible slabstock foam.

Active ingredient content min.: 99.3 %
Color number max.: 25 HU
Density at 20 °C: approx 0.90 g/cm³
Flash point approx.: 60 °C
Initial boiling point approx.: 180 °C
Pour point: < - 70 °C
Viscosity approx.: 26 mPa·s
Water content max.: 0.15 %

Addovate WM can be used as main catalyst for the production of flexible ester foam based mainly on TDI 65/35.
Addovate WM is used at 1.0 - 1.6 pphp, depending on the water content of the formulation (2.0 - 5.0 pphp).
Addovate WM is insoluble in water, it can be emulsified in a mixture of water, Addovate WM and Addovate SM.

Addovate WM helps to emulsify water, paraffin oil, and water-insoluble catalysts within polyester polyols.
Addovate WM is important to store Addovate WM in a cool, dry place away from direct sunlight and sources of ignition.
When handling Addovate WM, appropriate PPE such as gloves, goggles, and protective clothing should be worn to prevent skin and eye contact.

Disposal of Addovate WM should be conducted in accordance with local, regional, and national regulations.
The MSDS provides guidelines on the safe disposal of the product and any contaminated materials.
Addovate WM is compatible with polyester polyols, enhancing their processing characteristics.

Addovate WM is often used in combination with other additives such as Addovate SM and Addovate LM to achieve specific performance characteristics and prevent issues like core discoloration.
Accurate measurement and mixing are crucial for optimal performance.
The recommended dosages should be adhered to, and any adjustments should be made based on specific formulation requirements and performance outcomes.

Lanxess ensures that Addovate WM is manufactured under stringent quality control standards to maintain consistent performance and reliability.
Addovate WM provides technical support to customers, helping them optimize their formulations and resolve any processing challenges.
Detailed in the technical data sheet, crucial for determining the mixing and processing conditions.

Indicates the level of free acidity in the product, measured in mg KOH/g.
Specified under recommended storage conditions.
Add 1.0 - 2.0 parts by weight (p.b.w.) of Addovate WM to 100 p.b.w. of polyester polyol.

Can lead to reduced compression hardness.
Results in poor catalyst homogenization and potential cell structure damage.
Often used with Addovate SM and Addovate LM to prevent core discoloration and enhance foam quality.

Store in a cool, dry place away from direct sunlight and sources of ignition.
Use gloves, goggles, and protective clothing to prevent skin and eye contact.
Follow the guidelines in the MSDS for safe cleanup and disposal of spills.

Dispose of according to local, regional, and national regulations, as detailed in the MSDS.
Essential for ensuring uniform cell structure and consistent physical properties in the foam.
Ensures even distribution of water-insoluble catalysts, crucial for foam quality.

Reduces processing issues and defects, leading to higher production efficiency and reduced waste.
Provides technical support to help customers optimize formulations and resolve processing challenges.
Manufactured under stringent quality control standards to ensure consistent product performance.

Detailed in the Addovate WM, including potential environmental hazards and safe disposal practices.
Complies with relevant industry standards and regulations, as documented in the MSDS and TDS.
Available through Addovate WM and authorized distributors.

This emulsifier is used to ensure a homogeneous mixture of components, which is crucial for producing high-quality foam with a uniform cell structure.
Facilitates the mixing of water, paraffin oil, and catalysts in polyester polyols.

Polyester Slabstock Foam Production: Used in the production of flexible slabstock foam with TDI (Toluene Diisocyanate) 65.
Combination with Other Additives: Often used alongside Addovate SM and, if necessary, Addovate LM to prevent core discoloration and maintain the desired foam properties.
Addovate WM are added to 100 p.b.w. of polyester polyol.

Over-dosage (> 4.0 p.b.w.) can lead to a decrease in compression hardness, while under-dosage can result in poor homogenization and cell structure damage.
Addovate WM is a product of Lanxess, a company specializing in chemical production.
Primarily used in the production of polyester-based flexible slabstock foam.

Addovate WM emulsifies water, paraffin oil, and water-insoluble catalysts in polyester polyols.
This ensures a consistent and homogeneous mixture, which is critical for producing foam with uniform properties.
Suitable for polyester polyols with an OH-value of approximately 60 mg KOH/g.

Helps achieve a stable foam structure by preventing defects that can occur from poor emulsification.
Typically, 1.0 - 2.0 parts by weight (p.b.w.) of Addovate WM are added to 100 p.b.w. of polyester polyol.
Adding more than 4.0 p.b.w. can lead to a decrease in the compression hardness of the foam.

Insufficient amounts can cause poor homogenization of the catalyst mixture, leading to severe damage to the foam's cell structure.
Often used with Addovate SM and, if needed, Addovate LM to prevent core discoloration and to enhance foam stability.
If a silicone stabilizer does not sufficiently emulsify Addocat DB (a catalyst), it is recommended to add 0.5 - 1.0 p.b.w. of Addovate WM.

Uses:
Addovate WM is used automotive: Seating, headrests, and interior padding.
Addovate WM uniform catalyst distribution is crucial for maintaining consistent reaction rates and producing foam with uniform cell structure and physical properties.
Acts as a dispersant for various components, including water and paraffin oil, in the foam formulation.

Proper dispersion of these components is essential for achieving a homogeneous mixture, which leads to higher quality foam.
By ensuring thorough emulsification and dispersion, Addovate WM minimizes processing issues and defects, resulting in higher production efficiency.
Reduces waste and the need for rework, making the production process more cost-effective.

Often used in combination with other additives like Addovate SM and Addovate LM to achieve specific properties and prevent issues such as core discoloration.
Can be adjusted in various formulations to meet specific requirements, providing flexibility to manufacturers.
Ensures that the foam has a consistent cell structure, which is important for its mechanical properties and appearance.

Helps achieve uniform density, compression hardness, and other critical physical properties throughout the foam.
Improves the overall durability and performance of the foam products.
Used in R&D for developing new foam formulations and improving existing ones.

Helps in optimizing the production process and achieving desired foam characteristics through experimental adjustments.
Addovate WM is crucial in producing soft yet durable cushions and upholstery materials that retain their shape and comfort over time.
Used in creating high-quality foam mattresses that offer excellent support and comfort.

Ensures the production of comfortable and resilient car seats and headrests.
Used in various padding applications within vehicle interiors to enhance comfort and safety.
Helps in making products that provide additional comfort and support in bedding.

Produces foam packaging that protects delicate items during shipping and handling, ensuring their safe delivery.
Addovate WM is used in producing insulation foam that improves energy efficiency and thermal comfort in buildings.
Helps create soundproofing materials that reduce noise transmission in residential and commercial spaces.

Used in padding for garments, such as jackets and bras, to enhance comfort.
Addovate WM is used in producing foam components for items like cushions and pillows.
Ensures the uniform distribution of catalysts within the polyester polyols, which is essential for the consistent quality of the foam.

Proper emulsification prevents issues such as uneven cell structure and weak points in the foam.
Facilitates the even dispersion of water and paraffin oil within the foam formulation, which is crucial for achieving the desired foam characteristics.
Ensures a consistent cell structure, leading to superior mechanical properties and longevity of the foam.

Achieves uniformity in critical properties such as density, compression set, and rebound resilience.
Contributes to the production of durable foam products that withstand prolonged use without significant degradation.
Helps in producing foams that meet environmental standards and regulations.

Ensures that foam products comply with safety standards for use in consumer and industrial applications.
Comfort, durability, and aesthetic quality are enhanced in products like mattresses, cushions, and upholstery.
Addovate WM safety, comfort, and resilience in seating and interior padding.

Protection of sensitive items with cushioning that absorbs shocks and impacts.
Addovate WM improved energy efficiency and noise reduction in buildings with high-quality insulation and soundproofing materials.
Enhanced comfort and performance in padded garments and soft furnishings.

Helps in attaining specific physical properties by ensuring all components are evenly distributed.
Minimizes common processing issues such as phase separation and inconsistent mixing, leading to smoother production runs.
Reduces material wastage and the need for corrective measures, thereby saving costs and time.

When used with Addovate SM and Addovate LM, it helps prevent core discoloration, maintaining the aesthetic quality of the foam.
Allows manufacturers to tweak foam formulations to meet specific requirements, such as varying density or hardness.

Addovate WM is used Mattresses, mattress toppers, and pillows.
Addovate WM is used Protective foam packaging for delicate items.

Addovate WM is used Insulation materials and soundproofing panels.
Addovate WM is used Padding for garments and soft furnishings.
Addovate WM emulsifies water-insoluble catalysts, such as Addocat DB, ensuring even distribution within polyester polyols.

Addovate WM is predominantly used in the manufacturing of polyester-based flexible slabstock foam.
This type of foam is utilized in a variety of industries due to its versatility and beneficial properties.
Addovate WM is used cushions, mattresses, and upholstery.

Safety Profile:
Prolonged or repeated exposure to certain additives might cause skin or eye irritation, respiratory issues, or other health effects.
Depending on the chemical makeup, some additives can be flammable or pose a fire risk under certain conditions.

Some polymer additives can release hazardous chemicals during processing or application.
This might include respiratory irritants or sensitizers.
If not managed properly, disposal of polymer-based products can lead to environmental contamination.


ADDOVATE® 390

Addovate® 390 is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® 390 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addovate® 390 is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 68479-98-1
EC Number: 270-877-4

Synonyms: Polyurethane curing agent, Addovate® 390, Curing Agent 390, Addovate Polyurethane Curing Agent 390, PU Curing Agent 390, Polyurethane Additive 390, Curing Agent 390, Additive 390, PU Additive 390, Addovate PU Curing Agent 390



APPLICATIONS


Addovate® 390 is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addovate® 390 is essential in the manufacture of high-performance polyurethane adhesives.
Addovate® 390 is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addovate® 390 is a preferred curing agent for flexible and rigid foams due to its reactivity and efficiency.
Addovate® 390 is used in automotive coatings for its excellent adhesion and flexibility.
Addovate® 390 is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addovate® 390 is used in water-based polyurethane systems for its compatibility and stability.
Addovate® 390 is a key component in solvent-based polyurethane coatings.
Addovate® 390 is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addovate® 390 is employed in the production of rubber materials for its curing properties.
Addovate® 390 is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addovate® 390 is used in the construction industry for high-performance coatings and sealants.

Addovate® 390 is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addovate® 390 is a key component in the production of plastics, improving their mechanical properties.
Addovate® 390 is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addovate® 390 is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addovate® 390 is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addovate® 390 is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addovate® 390 is used in the production of rubber products, ensuring durable and consistent performance.
Addovate® 390 is employed in the automotive industry, used in high-performance coatings and adhesives.
Addovate® 390 is utilized in the production of wood coatings, enhancing their durability and appearance.

Addovate® 390 is found in the manufacture of specialty coatings for industrial machinery.
Addovate® 390 is utilized in the formulation of adhesives and sealants.
Addovate® 390 is a key ingredient in the production of polyurethane elastomers.

Addovate® 390 is employed in the textile industry to improve the performance of coatings on fabrics.
Addovate® 390 is used in the rubber industry for its curing properties.
Addovate® 390 is essential in the production of high-performance industrial coatings.

Addovate® 390 is a vital component in water-based and solvent-based polyurethane systems.
Addovate® 390 is applied in the creation of high-performance industrial products.
Addovate® 390 is used in the formulation of household and industrial coatings.

Addovate® 390 is utilized in the production of specialty coatings for electronic devices.
Addovate® 390 is found in the creation of specialty inks for various applications.
Addovate® 390 is used in the production of ceramic and glass coatings.

Addovate® 390 is applied in the creation of coatings for plastic surfaces.
Addovate® 390 is utilized in the formulation of coatings for wood surfaces.
Addovate® 390 is essential in the production of high-performance adhesives.

Addovate® 390 is used in the formulation of coatings for automotive applications.
Addovate® 390 is utilized in the production of specialty adhesives and sealants.
Addovate® 390 is found in the manufacture of coatings for industrial machinery.

Addovate® 390 is employed in the creation of specialty coatings for various substrates.
Addovate® 390 is used in the formulation of high-performance coatings for various applications.
Addovate® 390 is a key component in the production of specialty inks for flexographic and gravure printing.

Addovate® 390 is used in the creation of specialty inks for digital printing.
Addovate® 390 is essential in the production of high-performance industrial products.
Addovate® 390 is utilized in the manufacture of environmentally friendly industrial products.

Addovate® 390 is used in the creation of water-based and solvent-based products.
Addovate® 390 is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addovate® 390 is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® 390 is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addovate® 390 is a versatile chemical compound used in various polyurethane applications.
Addovate® 390 is known for its strong curing properties, which improve the durability and performance of polyurethane products.
Addovate® 390 provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addovate® 390 is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addovate® 390 is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addovate® 390's non-toxic nature makes it safe for use in various industrial and consumer products.

Addovate® 390 offers excellent weather resistance, making it suitable for outdoor applications.
Addovate® 390 is known for its ease of dispersion, ensuring uniform curing in various systems.
Addovate® 390 is essential in the creation of durable and high-performance polyurethane products.

Addovate® 390's strong curing properties make it a preferred choice in the creation of high-quality industrial coatings.
Addovate® 390 is an important precursor in the production of high-performance adhesives and sealants.
Addovate® 390 is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addovate® 390
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addovate® 390 is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addovate® 390.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addovate® 390 in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addovate® 390 at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addovate® 390 away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addovate® 390 to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOVATE® BA

Addovate® BA is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® BA is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addovate® BA is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 1338-23-4
EC Number: 215-661-2

Synonyms: Polyurethane curing agent, Addovate® BA, Curing Agent BA, Addovate Polyurethane Curing Agent BA, PU Curing Agent BA, Polyurethane Additive BA, Curing Agent BA, Additive BA, PU Additive BA, Addovate PU Curing Agent BA



APPLICATIONS


Addovate® BA is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addovate® BA is essential in the manufacture of high-performance polyurethane adhesives.
Addovate® BA is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addovate® BA is a preferred curing agent for flexible and rigid foams due to its reactivity and efficiency.
Addovate® BA is used in automotive coatings for its excellent adhesion and flexibility.
Addovate® BA is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addovate® BA is used in water-based polyurethane systems for its compatibility and stability.
Addovate® BA is a key component in solvent-based polyurethane coatings.
Addovate® BA is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addovate® BA is employed in the production of rubber materials for its curing properties.
Addovate® BA is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addovate® BA is used in the construction industry for high-performance coatings and sealants.

Addovate® BA is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addovate® BA is a key component in the production of plastics, improving their mechanical properties.
Addovate® BA is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addovate® BA is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addovate® BA is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addovate® BA is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addovate® BA is used in the production of rubber products, ensuring durable and consistent performance.
Addovate® BA is employed in the automotive industry, used in high-performance coatings and adhesives.
Addovate® BA is utilized in the production of wood coatings, enhancing their durability and appearance.

Addovate® BA is found in the manufacture of specialty coatings for industrial machinery.
Addovate® BA is utilized in the formulation of adhesives and sealants.
Addovate® BA is a key ingredient in the production of polyurethane elastomers.

Addovate® BA is employed in the textile industry to improve the performance of coatings on fabrics.
Addovate® BA is used in the rubber industry for its curing properties.
Addovate® BA is essential in the production of high-performance industrial coatings.

Addovate® BA is a vital component in water-based and solvent-based polyurethane systems.
Addovate® BA is applied in the creation of high-performance industrial products.
Addovate® BA is used in the formulation of household and industrial coatings.

Addovate® BA is utilized in the production of specialty coatings for electronic devices.
Addovate® BA is found in the creation of specialty inks for various applications.
Addovate® BA is used in the production of ceramic and glass coatings.

Addovate® BA is applied in the creation of coatings for plastic surfaces.
Addovate® BA is utilized in the formulation of coatings for wood surfaces.
Addovate® BA is essential in the production of high-performance adhesives.

Addovate® BA is used in the formulation of coatings for automotive applications.
Addovate® BA is utilized in the production of specialty adhesives and sealants.
Addovate® BA is found in the manufacture of coatings for industrial machinery.

Addovate® BA is employed in the creation of specialty coatings for various substrates.
Addovate® BA is used in the formulation of high-performance coatings for various applications.
Addovate® BA is a key component in the production of specialty inks for flexographic and gravure printing.

Addovate® BA is used in the creation of specialty inks for digital printing.
Addovate® BA is essential in the production of high-performance industrial products.
Addovate® BA is utilized in the manufacture of environmentally friendly industrial products.

Addovate® BA is used in the creation of water-based and solvent-based products.
Addovate® BA is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addovate® BA is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® BA is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addovate® BA is a versatile chemical compound used in various polyurethane applications.
Addovate® BA is known for its strong curing properties, which improve the durability and performance of polyurethane products.
Addovate® BA provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addovate® BA is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addovate® BA is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addovate® BA's non-toxic nature makes it safe for use in various industrial and consumer products.

Addovate® BA offers excellent weather resistance, making it suitable for outdoor applications.
Addovate® BA is known for its ease of dispersion, ensuring uniform curing in various systems.
Addovate® BA is essential in the creation of durable and high-performance polyurethane products.

Addovate® BA's strong curing properties make it a preferred choice in the creation of high-quality industrial coatings.
Addovate® BA is an important precursor in the production of high-performance adhesives and sealants.
Addovate® BA is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addovate® BA
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.0 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addovate® BA is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addovate® BA.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.


Storage:

Store Addovate® BA in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.

Storage:
Temperature:
Store Addovate® BA at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addovate® BA away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addovate® BA to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADDOVATE® LP

Addovate® LP is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® LP is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.
The chemical formula for Addovate® LP is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 123-31-9
EC Number: 204-617-8

Synonyms: Polyurethane curing agent, Addovate® LP, Curing Agent LP, Addovate Polyurethane Curing Agent LP, PU Curing Agent LP, Polyurethane Additive LP, Curing Agent LP, Additive LP, PU Additive LP, Addovate PU Curing Agent LP



APPLICATIONS


Addovate® LP is widely used in the formulation of polyurethane coatings, providing excellent durability and chemical resistance.
Addovate® LP is essential in the manufacture of high-performance polyurethane adhesives.
Addovate® LP is utilized in the production of elastomers, enhancing their mechanical properties and longevity.

Addovate® LP is a preferred curing agent for flexible and rigid foams due to its reactivity and efficiency.
Addovate® LP is used in automotive coatings for its excellent adhesion and flexibility.
Addovate® LP is found in the production of sealants and caulks, contributing to their strength and elasticity.

Addovate® LP is used in water-based polyurethane systems for its compatibility and stability.
Addovate® LP is a key component in solvent-based polyurethane coatings.
Addovate® LP is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addovate® LP is employed in the production of rubber materials for its curing properties.
Addovate® LP is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addovate® LP is used in the construction industry for high-performance coatings and sealants.

Addovate® LP is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addovate® LP is a key component in the production of plastics, improving their mechanical properties.
Addovate® LP is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addovate® LP is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addovate® LP is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addovate® LP is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addovate® LP is used in the production of rubber products, ensuring durable and consistent performance.
Addovate® LP is employed in the automotive industry, used in high-performance coatings and adhesives.
Addovate® LP is utilized in the production of wood coatings, enhancing their durability and appearance.

Addovate® LP is found in the manufacture of specialty coatings for industrial machinery.
Addovate® LP is utilized in the formulation of adhesives and sealants.
Addovate® LP is a key ingredient in the production of polyurethane elastomers.

Addovate® LP is employed in the textile industry to improve the performance of coatings on fabrics.
Addovate® LP is used in the rubber industry for its curing properties.
Addovate® LP is essential in the production of high-performance industrial coatings.

Addovate® LP is a vital component in water-based and solvent-based polyurethane systems.
Addovate® LP is applied in the creation of high-performance industrial products.
Addovate® LP is used in the formulation of household and industrial coatings.

Addovate® LP is utilized in the production of specialty coatings for electronic devices.
Addovate® LP is found in the creation of specialty inks for various applications.
Addovate® LP is used in the production of ceramic and glass coatings.

Addovate® LP is applied in the creation of coatings for plastic surfaces.
Addovate® LP is utilized in the formulation of coatings for wood surfaces.
Addovate® LP is essential in the production of high-performance adhesives.

Addovate® LP is used in the formulation of coatings for automotive applications.
Addovate® LP is utilized in the production of specialty adhesives and sealants.
Addovate® LP is found in the manufacture of coatings for industrial machinery.

Addovate® LP is employed in the creation of specialty coatings for various substrates.
Addovate® LP is used in the formulation of high-performance coatings for various applications.
Addovate® LP is a key component in the production of specialty inks for flexographic and gravure printing.

Addovate® LP is used in the creation of specialty inks for digital printing.
Addovate® LP is essential in the production of high-performance industrial products.
Addovate® LP is utilized in the manufacture of environmentally friendly industrial products.

Addovate® LP is used in the creation of water-based and solvent-based products.
Addovate® LP is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addovate® LP is a high-performance curing agent used in polyurethane systems for its excellent reactivity and versatility.
Addovate® LP is characterized by its stability and efficiency in enhancing the mechanical properties of polyurethane products.

Addovate® LP is a versatile chemical compound used in various polyurethane applications.
Addovate® LP is known for its strong curing properties, which improve the durability and performance of polyurethane products.
Addovate® LP provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addovate® LP is compatible with a wide range of polyurethane systems, enhancing its versatility in different formulations.
Addovate® LP is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addovate® LP's non-toxic nature makes it safe for use in various industrial and consumer products.

Addovate® LP offers excellent weather resistance, making it suitable for outdoor applications.
Addovate® LP is known for its ease of dispersion, ensuring uniform curing in various systems.
Addovate® LP is essential in the creation of durable and high-performance polyurethane products.

Addovate® LP's strong curing properties make it a preferred choice in the creation of high-quality industrial coatings.
Addovate® LP is an important precursor in the production of high-performance adhesives and sealants.
Addovate® LP is widely used in the manufacture of durable and resilient polyurethane products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addovate® LP
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.1 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polyurethane systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addovate® LP is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addovate® LP.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.


Storage:

Store Addovate® LP in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.

Storage:
Temperature:
Store Addovate® LP at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addovate® LP away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addovate® LP to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

ADDOVATE® THERMOSTAB

Addovate® Thermostab is a high-performance stabilizer used in various polymer applications for its excellent thermal stability and versatility.
Addovate® Thermostab is characterized by its stability and efficiency in enhancing the durability and longevity of polymer products.
The chemical formula for Addovate® Thermostab is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 68555-53-8
EC Number: 271-374-3

Synonyms: Thermal stabilizer, Addovate® Thermostab, Polymer stabilizer, Addovate Polymer Stabilizer, Thermal Resistance Agent, Polymer Additive Thermostab, Stabilizer Thermostab, Addovate Thermal Stabilizer, PU Stabilizer Thermostab, Additive Thermostab



APPLICATIONS


Addovate® Thermostab is widely used in the stabilization of polyurethane products, providing excellent thermal stability and durability.
Addovate® Thermostab is essential in the manufacture of high-performance polyurethane foams.
Addovate® Thermostab is utilized in the production of elastomers, enhancing their thermal stability and longevity.

Addovate® Thermostab is a preferred stabilizer for flexible and rigid foams due to its reactivity and efficiency.
Addovate® Thermostab is used in automotive applications for its excellent stability and performance under high temperatures.
Addovate® Thermostab is found in the production of coatings and sealants, contributing to their durability and thermal resistance.

Addovate® Thermostab is used in water-based polymer systems for its compatibility and stability.
Addovate® Thermostab is a key component in solvent-based polyurethane coatings.
Addovate® Thermostab is used in the textile industry to improve the durability and performance of coatings on fabrics.

Addovate® Thermostab is employed in the production of rubber materials for its stabilizing properties.
Addovate® Thermostab is used in the manufacturing of synthetic fibers, enhancing their strength and resilience.
Addovate® Thermostab is used in the construction industry for high-performance coatings and sealants.

Addovate® Thermostab is used in the creation of high-performance adhesives, providing strong and durable bonds.
Addovate® Thermostab is a key component in the production of plastics, improving their mechanical properties.
Addovate® Thermostab is utilized in the formulation of industrial coatings, ensuring durability and chemical resistance.

Addovate® Thermostab is applied in the creation of specialty coatings for various industrial applications, ensuring durability and performance.
Addovate® Thermostab is used in the production of coatings for metal surfaces, providing corrosion resistance.
Addovate® Thermostab is essential in the creation of high-quality printing inks, enhancing adhesion and flexibility.

Addovate® Thermostab is used in the production of rubber products, ensuring durable and consistent performance.
Addovate® Thermostab is employed in the automotive industry, used in high-performance coatings and adhesives.
Addovate® Thermostab is utilized in the production of wood coatings, enhancing their durability and appearance.

Addovate® Thermostab is found in the manufacture of specialty coatings for industrial machinery.
Addovate® Thermostab is utilized in the formulation of adhesives and sealants.
Addovate® Thermostab is a key ingredient in the production of polyurethane elastomers.

Addovate® Thermostab is employed in the textile industry to improve the performance of coatings on fabrics.
Addovate® Thermostab is used in the rubber industry for its stabilizing properties.
Addovate® Thermostab is essential in the production of high-performance industrial coatings.

Addovate® Thermostab is a vital component in water-based and solvent-based polymer systems.
Addovate® Thermostab is applied in the creation of high-performance industrial products.
Addovate® Thermostab is used in the formulation of household and industrial coatings.

Addovate® Thermostab is utilized in the production of specialty coatings for electronic devices.
Addovate® Thermostab is found in the creation of specialty inks for various applications.
Addovate® Thermostab is used in the production of ceramic and glass coatings.

Addovate® Thermostab is applied in the creation of coatings for plastic surfaces.
Addovate® Thermostab is utilized in the formulation of coatings for wood surfaces.
Addovate® Thermostab is essential in the production of high-performance adhesives.

Addovate® Thermostab is used in the formulation of coatings for automotive applications.
Addovate® Thermostab is utilized in the production of specialty adhesives and sealants.
Addovate® Thermostab is found in the manufacture of coatings for industrial machinery.

Addovate® Thermostab is employed in the creation of specialty coatings for various substrates.
Addovate® Thermostab is used in the formulation of high-performance coatings for various applications.
Addovate® Thermostab is a key component in the production of specialty inks for flexographic and gravure printing.

Addovate® Thermostab is used in the creation of specialty inks for digital printing.
Addovate® Thermostab is essential in the production of high-performance industrial products.
Addovate® Thermostab is utilized in the manufacture of environmentally friendly industrial products.

Addovate® Thermostab is used in the creation of water-based and solvent-based products.
Addovate® Thermostab is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces.



DESCRIPTION


Addovate® Thermostab is a high-performance stabilizer used in various polymer applications for its excellent thermal stability and versatility.
Addovate® Thermostab is characterized by its stability and efficiency in enhancing the durability and longevity of polymer products.

Addovate® Thermostab is a versatile chemical compound used in various polymer applications.
Addovate® Thermostab is known for its strong stabilizing properties, which improve the durability and performance of polymer products.
Addovate® Thermostab provides excellent chemical resistance, making it ideal for industrial coatings and adhesives.

Addovate® Thermostab is compatible with a wide range of polymer systems, enhancing its versatility in different formulations.
Addovate® Thermostab is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Addovate® Thermostab's non-toxic nature makes it safe for use in various industrial and consumer products.

Addovate® Thermostab offers excellent weather resistance, making it suitable for outdoor applications.
Addovate® Thermostab is known for its ease of dispersion, ensuring uniform stabilizing in various systems.
Addovate® Thermostab is essential in the creation of durable and high-performance polymer products.

Addovate® Thermostab's strong stabilizing properties make it a preferred choice in the creation of high-quality industrial coatings.
Addovate® Thermostab is an important precursor in the production of high-performance adhesives and sealants.
Addovate® Thermostab is widely used in the manufacture of durable and resilient polymer products.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Addovate® Thermostab
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.0 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: High
Chemical Stability: Excellent
Compatibility: Wide range of polymer systems
Weather Resistance: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Addovate® Thermostab is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Addovate® Thermostab.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Addovate® Thermostab in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Addovate® Thermostab at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Addovate® Thermostab away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Addovate® Thermostab to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

ADENOPHORA TRIPHYLLA ROOT EXTRACT

Adenophora Triphylla Root Extract is a natural botanical ingredient derived from the root of the Adenophora Triphylla plant, known for its soothing and moisturizing properties.
Adenophora Triphylla Root Extract is recognized for its ability to calm irritated skin, enhance hydration, and support overall skin health, making it a valuable addition to skincare formulations.
This versatile extract offers both therapeutic and cosmetic benefits, helping to maintain healthy, smooth, and radiant skin.

CAS Number: 90082-38-9
EC Number: 290-105-6

Synonyms: Adenophora Triphylla Root Extract, Ladybell Root Extract, Adenophora Root Extract, Adenophora Triphylla Extract, Adenophora Root Essence, Ladybell Extract, Nodal Root Extract, Balloon Flower Root Extract, Adenophora Root Powder, Adenophora Triphylla Root Concentrate, Adenophora Triphylla Botanical Extract, Adenophora Phytoextract, Adenophora Triphylla Phytocomplex, Adenophora Bioactive Extract, Adenophora Root Phytoactives, Adenophora Triphylla Active, Adenophora Moisturizing Extract, Adenophora Triphylla Soothing Agent, Adenophora Triphylla Skin Care Active



APPLICATIONS


Adenophora Triphylla Root Extract is extensively used in the formulation of moisturizing creams, providing deep hydration and calming benefits for dry and sensitive skin.
Adenophora Triphylla Root Extract is favored in the creation of soothing serums, where it helps to reduce redness and irritation while enhancing skin comfort.
Adenophora Triphylla Root Extract is utilized in the development of face masks, offering intensive hydration and soothing effects that leave the skin feeling refreshed.

Adenophora Triphylla Root Extract is widely used in the production of night creams, where it supports the skin's natural repair processes and provides moisture throughout the night.
Adenophora Triphylla Root Extract is employed in the formulation of eye creams, providing gentle hydration and soothing care for the delicate skin around the eyes.
Adenophora Triphylla Root Extract is essential in the creation of lotions for sensitive skin, offering lightweight hydration and relief from irritation.

Adenophora Triphylla Root Extract is utilized in the production of after-sun products, providing calming and moisturizing benefits to sun-exposed skin.
Adenophora Triphylla Root Extract is a key ingredient in the formulation of anti-redness treatments, offering targeted care that minimizes visible redness and discomfort.
Adenophora Triphylla Root Extract is used in the creation of hydrating serums, where it enhances skin moisture levels and improves overall skin texture.

Adenophora Triphylla Root Extract is applied in the formulation of facial mists, offering a quick and refreshing way to hydrate and soothe the skin throughout the day.
Adenophora Triphylla Root Extract is employed in the production of body lotions, providing all-over hydration and protection for dry and irritated skin.
Adenophora Triphylla Root Extract is used in the development of calming creams, providing deep relief and hydration for sensitive and reactive skin.

Adenophora Triphylla Root Extract is widely utilized in the formulation of scalp treatments, providing hydration and soothing care that supports scalp health and comfort.
Adenophora Triphylla Root Extract is a key component in the creation of prebiotic skincare products, supporting the skin’s microbiome while providing hydration and soothing benefits.
Adenophora Triphylla Root Extract is used in the production of lip care products, providing hydration and protection for soft, smooth lips.

Adenophora Triphylla Root Extract is employed in the formulation of hand creams, offering hydration and soothing care that helps to maintain skin softness and reduce irritation.
Adenophora Triphylla Root Extract is applied in the creation of daily wear creams, offering balanced hydration and protection for everyday use.
Adenophora Triphylla Root Extract is utilized in the development of skin repair treatments, providing intensive care that helps to restore and protect damaged or irritated skin.

Adenophora Triphylla Root Extract is found in the formulation of facial oils, offering nourishing care that supports skin health and reduces sensitivity.
Adenophora Triphylla Root Extract is used in the production of soothing gels, providing instant relief from irritation and helping to calm reactive skin.
Adenophora Triphylla Root Extract is a key ingredient in the creation of multipurpose balms, providing versatile care for sensitive areas such as lips, hands, and face.

Adenophora Triphylla Root Extract is widely used in the formulation of anti-inflammatory skincare products, offering soothing and protective benefits for sensitive skin.
Adenophora Triphylla Root Extract is employed in the development of nourishing body butters, offering rich hydration and protection for dry, rough skin.
Adenophora Triphylla Root Extract is applied in the production of anti-aging serums, offering deep hydration and soothing care that helps to maintain youthful-looking skin.

Adenophora Triphylla Root Extract is utilized in the creation of facial oils, offering nourishing care that supports skin health and reduces oxidative stress.
Adenophora Triphylla Root Extract is found in the formulation of sensitive skin repair treatments, providing targeted care for areas prone to irritation and discomfort.
Adenophora Triphylla Root Extract is used in the production of sun care products, providing hydration and soothing care that preserves skin health.



DESCRIPTION


Adenophora Triphylla Root Extract is a natural botanical ingredient derived from the root of the Adenophora Triphylla plant, known for its soothing and moisturizing properties.
Adenophora Triphylla Root Extract is recognized for its ability to calm irritated skin, enhance hydration, and support overall skin health, making it a valuable addition to skincare formulations.

Adenophora Triphylla Root Extract offers additional benefits such as improving skin texture and promoting a healthy skin barrier, ensuring long-lasting comfort and protection.
Adenophora Triphylla Root Extract is often incorporated into formulations designed to provide comprehensive care for sensitive and dry skin, offering both immediate and long-term benefits.
Adenophora Triphylla Root Extract is recognized for its ability to enhance the overall health and appearance of the skin, leaving it smooth, hydrated, and radiant.

Adenophora Triphylla Root Extract is commonly used in both traditional and innovative skincare formulations, providing a reliable solution for maintaining healthy, hydrated skin.
Adenophora Triphylla Root Extract is valued for its ability to support the skin's natural moisture balance, making it a key ingredient in products that aim to protect and soothe the skin.
Adenophora Triphylla Root Extract is a versatile ingredient that can be used in a variety of products, including creams, lotions, serums, and oils.

Adenophora Triphylla Root Extract is an ideal choice for products targeting sensitive, dry, and irritated skin, as it provides gentle yet effective hydration and soothing care.
Adenophora Triphylla Root Extract is known for its compatibility with other skincare actives, allowing it to be easily integrated into multi-functional formulations.
Adenophora Triphylla Root Extract is often chosen for formulations that require a balance between hydration, protection, and soothing care, ensuring comprehensive skin benefits.

Adenophora Triphylla Root Extract enhances the overall effectiveness of personal care products by providing deep hydration, soothing relief, and skin protection in one ingredient.
Adenophora Triphylla Root Extract is a reliable ingredient for creating products that offer a pleasant user experience, with noticeable improvements in skin comfort and moisture levels.
Adenophora Triphylla Root Extract is an essential component in innovative skincare products that stand out in the market for their performance, safety, and ability to soothe and hydrate the skin.



PROPERTIES


Chemical Formula: N/A (Natural extract)
Common Name: Adenophora Triphylla Root Extract (Ladybell Root Extract)
Molecular Structure:
Appearance: Light yellow to brown liquid or powder
Density: Approx. 1.00-1.05 g/cm³ (for liquid extract)
Melting Point: N/A (liquid or powder form)
Solubility: Soluble in water and alcohols; insoluble in oils
Flash Point: >100°C (for liquid extract)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low (for liquid extract)



FIRST AID


Inhalation:
If Adenophora Triphylla Root Extract is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of eye contact, flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
If Adenophora Triphylla Root Extract is ingested, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of vapors.

Ventilation:
Ensure adequate ventilation when handling large amounts of Adenophora Triphylla Root Extract to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Adenophora Triphylla Root Extract.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Adenophora Triphylla Root Extract in a cool, dry, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid inhalation of vapors and direct contact with skin and eyes.
Use explosion-proof equipment in areas where vapors may be present.


Storage:

Temperature:
Store Adenophora Triphylla Root Extract at temperatures between 15-25°C as recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Adenophora Triphylla Root Extract away from incompatible materials, including strong oxidizers.

Handling Equipment:
Use dedicated equipment for handling Adenophora Triphylla Root Extract to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of cosmetic ingredients.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADIMOLL® DO

Adimoll® DO is a high-performance plasticizer used in various polymer applications for its excellent flexibility and compatibility.
Adimoll® DO is characterized by its ability to enhance the flexibility and durability of polymer products.
The chemical formula for Adimoll® DO is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 6422-86-2
EC Number: 229-176-9

Synonyms: Plasticizer, Adimoll® DO, Polymer plasticizer, Adimoll Polymer Plasticizer DO, Plasticizing Agent DO, Polymer Additive DO, Plasticizer Additive DO, PU Plasticizer DO, Adimoll Plasticizer DO, Flexible Additive DO



APPLICATIONS


Adimoll® DO is widely used in the formulation of flexible PVC products, providing excellent flexibility and durability.
Adimoll® DO is essential in the manufacture of high-performance polyurethane foams, enhancing their flexibility.
Adimoll® DO is utilized in the production of elastomers, improving their flexibility and longevity.

Adimoll® DO is a preferred plasticizer for flexible and rigid foams due to its efficiency in enhancing flexibility.
Adimoll® DO is used in automotive applications for its excellent flexibility and durability under various conditions.
Adimoll® DO is found in the production of sealants and caulks, contributing to their flexibility and performance.

Adimoll® DO is used in water-based polymer systems for its compatibility and efficiency in enhancing flexibility.
Adimoll® DO is a key component in solvent-based polymer formulations, providing improved flexibility.
Adimoll® DO is used in the textile industry to improve the flexibility and performance of coatings on fabrics.

Adimoll® DO is employed in the production of rubber materials for its plasticizing properties.
Adimoll® DO is used in the manufacturing of synthetic fibers, enhancing their flexibility and resilience.
Adimoll® DO is used in the construction industry for high-performance coatings and sealants.

Adimoll® DO is used in the creation of high-performance adhesives, providing improved flexibility and durability.
Adimoll® DO is a key component in the production of plastics, enhancing their flexibility and mechanical properties.
Adimoll® DO is utilized in the formulation of industrial coatings, ensuring improved flexibility and performance.

Adimoll® DO is applied in the creation of specialty coatings for various industrial applications, ensuring enhanced flexibility and performance.
Adimoll® DO is used in the production of coatings for metal surfaces, providing improved flexibility and durability.
Adimoll® DO is essential in the creation of high-quality printing inks, enhancing flexibility and performance during printing.

Adimoll® DO is used in the production of rubber products, ensuring consistent flexibility and performance.
Adimoll® DO is employed in the automotive industry, used in high-performance coatings and adhesives for improved flexibility.
Adimoll® DO is utilized in the production of wood coatings, enhancing their flexibility and durability.

Adimoll® DO is found in the manufacture of specialty coatings for industrial machinery, providing improved flexibility and performance.
Adimoll® DO is utilized in the formulation of adhesives and sealants, ensuring enhanced flexibility and performance.
Adimoll® DO is a key ingredient in the production of polyurethane elastomers, enhancing their flexibility and longevity.

Adimoll® DO is employed in the textile industry to improve the performance and flexibility of coatings on fabrics.
Adimoll® DO is used in the rubber industry for its plasticizing properties, improving flexibility and performance.
Adimoll® DO is essential in the production of high-performance industrial coatings, providing improved flexibility and durability.

Adimoll® DO is a vital component in water-based and solvent-based polymer systems, ensuring enhanced flexibility and performance.
Adimoll® DO is applied in the creation of high-performance industrial products, providing improved flexibility and durability.
Adimoll® DO is used in the formulation of household and industrial coatings, enhancing their flexibility and performance.

Adimoll® DO is utilized in the production of specialty coatings for electronic devices, providing improved flexibility.
Adimoll® DO is found in the creation of specialty inks for various applications, enhancing flexibility and performance.
Adimoll® DO is used in the production of ceramic and glass coatings, improving their flexibility and application properties.

Adimoll® DO is applied in the creation of coatings for plastic surfaces, ensuring improved flexibility and performance.
Adimoll® DO is utilized in the formulation of coatings for wood surfaces, providing enhanced flexibility and durability.
Adimoll® DO is essential in the production of high-performance adhesives, ensuring improved flexibility and application properties.

Adimoll® DO is used in the formulation of coatings for automotive applications, providing improved flexibility and performance.
Adimoll® DO is utilized in the production of specialty adhesives and sealants, ensuring enhanced flexibility and durability.
Adimoll® DO is found in the manufacture of coatings for industrial machinery, providing improved flexibility and performance.

Adimoll® DO is employed in the creation of specialty coatings for various substrates, ensuring improved flexibility and performance.
Adimoll® DO is used in the formulation of high-performance coatings for various applications, providing enhanced flexibility and performance.
Adimoll® DO is a key component in the production of specialty inks for flexographic and gravure printing, ensuring improved flexibility and performance.

Adimoll® DO is used in the creation of specialty inks for digital printing, providing enhanced flexibility and application properties.
Adimoll® DO is essential in the production of high-performance industrial products, ensuring improved flexibility and performance.
Adimoll® DO is utilized in the manufacture of environmentally friendly industrial products, providing enhanced flexibility and durability.

Adimoll® DO is used in the creation of water-based and solvent-based products, ensuring improved flexibility and performance.
Adimoll® DO is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces, providing enhanced flexibility and application properties.



DESCRIPTION


Adimoll® DO is a high-performance plasticizer used in various polymer applications for its excellent flexibility and compatibility.
Adimoll® DO is characterized by its ability to enhance the flexibility and durability of polymer products.

Adimoll® DO is a versatile chemical compound used in various polymer applications.
Adimoll® DO is known for its strong plasticizing properties, which improve the flexibility and performance of polymer products.
Adimoll® DO provides excellent compatibility with a wide range of polymers, making it ideal for industrial coatings and adhesives.

Adimoll® DO is compatible with a wide range of polymer systems, enhancing its versatility in different formulations.
Adimoll® DO is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Adimoll® DO's non-toxic nature makes it safe for use in various industrial and consumer products.

Adimoll® DO offers excellent flexibility, making it suitable for applications requiring enhanced flexibility and durability.
Adimoll® DO is known for its ease of dispersion, ensuring uniform plasticizing in various systems.
Adimoll® DO is essential in the creation of durable and high-performance polymer products.

Adimoll® DO's strong plasticizing properties make it a preferred choice in the creation of high-quality industrial coatings.
Adimoll® DO is an important precursor in the production of high-performance adhesives and sealants, providing improved flexibility.
Adimoll® DO is widely used in the manufacture of durable and resilient polymer products, ensuring enhanced flexibility and performance.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Adimoll® DO
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 0.99 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: Low
Chemical Stability: Excellent
Compatibility: Wide range of polymer systems
Flexibility: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Adimoll® DO is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Adimoll® DO.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Adimoll® DO in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Adimoll® DO at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Adimoll® DO away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Adimoll® DO to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.
ADIPIC ACID
Adipic Acid also known as Hexane-1,6-dioic acid is a dibasic acid with the molecular formula C3H8O4, CAS 124-04-9.
Adipic acid is slightly soluble in water and soluble in alcohol and acetone.
Adipic Acid is the most important dicarboxylic acid with roughly 2.5 billion kilograms produced annually and mainly used as a precursor to nylon production.

CAS Number: 124-04-9
EC Number: 204-673-3
Molecular Formula: C6H10O4
Molar Mass: 146.14 g/mol

Adipic Acid, also known as hexanedioic acid, is a dicarboxylic acid.
Adipic Acid is an intermediate for nylon and a precursor in the synthesis of polyester polyols for polyurethane systems and thermoplastic polyurethanes.
Adipic Acid is colorless crystalline powder.

Adipic acid is an organic dicarboxylic acid. Available in various quantities, Adipic Acid is used as a monomer in nylon production.
Other applications include use as a monomer for polyurethane production, a component of controlled-release drugs, and a food additive.

Adipic Acid, solid white powder, is a very important organic compound for today chemical industry.
Adipic Acid (AA), CAS number is 124-04-9, is a dicarboxylic acid with the formula: (CH2)4(COOH)2; for the chemical point of view, 1,6 Hexanedioic acid.

The main Adipic Acid application is the production of nylon by a polycondensation reaction.
Nylons are produced by the reaction of bifunctional monomers containing equal parts of amine and carboxylic acid.
Besides the production of Nylon 6,6 as well as specialty nylon grades, Adipic Acid, CAS 124-04-9, finds many other applications, like polyester polyols for polyurethanes (PU), manufacturing of resins for paper products, unsaturated polyester resins, adipates production, plasticizers for PVC and a small share of the market is ingredient for food and medication.

90% of adipic acid is consumed in the industry for the production of nylon by poly-condensation with hexamethylenediamine.
Adipic Acid is mainly used for the production of nylon 6,6 polymer for fibers and plastics.

Nylon has a protein-like structure.
Adipic Acid can be further processed into the fibers for applications in carpets (felts), automobile tire cords and clothing.

Adipic Acid can be used in the production of adipic acid plasticizer and lubricant components.
Adipic Acid can be used in the production of polyester polyols for polyurethane systems.

Technical grade adipic acid can be used to produce plasticizers, to add flexibility and to give flexibility to unsaturated polyesters.
Adipic Acid can be used in the production of rigid and flexible foams, in the production of wire coaters, elastomers and adhesives, to increase the flexibility of alkyd resins, in the production of wet strong resins and in the production of synthetic lubricants and oils for the paper chemical industry.

Adipic acid, mol wt 146.14, HOOCCH2CH2CH,CH2COOH, is a white crystalline solid with a melting point of about 152°C.
Little of this dicarboxylic acid occurs naturally, but Adipic Acid is produced on a very large scale at several locations around the world.

The majority of this material is used in the manufacture of Nylon-6,6 polyamide, which is prepared by reaction with 1,6-hexanediamine.
Adipic acid is a colorless, odorless, sour-tasting crystalline solid that undergoes reactions including esterification, amidation, reduction, halogenation, salt formation, and dehydration.

Adipic Acid also undergoes several industrially significant polymerization reactions.
Adipic acid historically has been manufactured predominantly from cyclohexane.
However, much research continues to be directed to alternative feedstocks, especially butadiene and cyclohexene, as dictated by shifts in hydrocarbon pricing.

Air quality regulations may exert further pressure for alternative routes as manufacturers seek to avoid NOx abatement costs.
When dispersed as a dust, adipic acid is subject to normal dust explosion hazards.

The material is an irritant, especially upon contact with the mucous membranes.
Protective goggles or face shields should be worn when handling the material.

The material should be stored in corrosion-resistant containers, away from alkaline or strong oxidizing materials.
Adipic acid is a very large-volume organic chemical and is one of the top 50 chemicals produced in the United States in terms of volume, although demand is highly cyclic.

Adipic acid for nylon takes ∼60% of U.S. cyclohexane production.
Adipic acid is relatively nontoxic.

Adipic acid is an important inudstrial dicarboxylic acid with about 2.5 billion kilograms produced per year.
Adipic Acid is used mainly in the production of nylon.
Adipic Acid occurs relatively rarely in nature.

Adipic Acid has a tart taste and is also used as an additive and gelling agent in jello or gelatins.
Adipic Acid is also used in some calcium carbonate antacids to make them tart.

Adipic acid has also been incorporated into controlled-release formulation matrix tablets to obtain pH-independent release for both weakly basic and weakly acidic drugs.
Adipic acid in the urine and in the blood is typically exogenous in origin and is a good biomarker of jello consumption.

In fact, a condition known as adipic aciduria is actually an artifact of jello consumption.
However, certain disorders (such as diabetes and glutaric aciduria type I.) can lead to elevated levels of adipic acid snd other dicarboxcylic acids (such as suberic acid) in urine.

Moreover, adipic acid is also found to be associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, carnitine-acylcarnitine translocase deficiency, malonyl-Coa decarboxylase deficiency, and medium Chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism.
Adipic acid is also microbial metabolite found in Escherichia.

Adipic acid or hexanedioic acid is the organic compound with the formula (CH2)4(COOH)2.
From an industrial perspective, Adipic Acid is the most important dicarboxylic acid: about 2.5 billion kilograms of this white crystalline powder are produced annually, mainly as a precursor for the production of nylon.

Adipic acid otherwise rarely occurs in nature, but Adipic Acid is known as manufactured E number food additive E355.
Salts and esters of adipic acid are known as adipates.

Adipic acid is a white crystalline solid.
Adipic Acid is insoluble in water.

The primary hazard is the threat to the environment.
Immediate steps should be taken to limit Adipic Acid spread to the environment.
Adipic Acid is used to make plastics and foams and for other uses.

Adipic acid is a straight-chain aliphatic dicarboxylic acid, commonly used in the manufacturing of nylon-6,6 and plasticizers.
Conventionally Adipic Acid was manufactured from petrochemicals but in recent days Adipic Acid can be synthesized from renewable substrates by means of biological methods.

Adipic acid, or more formally hexanedioic acid, is a white crystalline solid that melts at 152 ºC.
Adipic Acid is one of the most important monomers in the polymer industry.

Adipic acid is found in beet juice, but the article of commerce—≈2.5 million tonnes of Adipic Acid per year—is manufactured.
In 1906, French chemists L. Bouveault and R. Locquin reported that adipic acid can be produced by oxidizing cyclohexanol.
Today, the most common manufacturing process is the nitric acid (HNO3) oxidation of a cyclohexanol–cyclohexanone mixture called KA (for ketone–alcohol) oil.

Almost all adipic acid is used as a comonomer with hexamethylenediamine to produce nylon 6-6.
Adipic Acid is also used to manufacture other polymers such as polyurethanes.

Using HNO3 to produce Adipic Acid has its downside: Copious amounts of nitrous oxide (N2O), a greenhouse gas, are coproduced and released into the atmosphere.
In late 2014, K. C. Hwang and A. Sagadevan of National Tsing Hua University (Hsinchu City, Taiwan) reported a process that uses ozone and ultraviolet (UV) light to oxidize KA oil to adipic acid.

This method eliminates the production of N2O.
But before the process can be used commercially, problems associated with the formation of organic peroxides from ozone and the difficulty of using UV light on a large scale must be overcome.

Applications of Adipic Acid:
Adipic Acid is used to make nylon, polyurethane foams, lubricants, and plasticizers.
Adipic Acid is used in adhesives, baking powder, and food flavoring.

The major markets for adipic acid include use as feedstocks for nylon 6,6 resins and fibers, polyester polyols and plasticzers.
Documented applications for adipic acid are as a lubricant additive in coatings and foams and shoe soles, as a tanning agent in the leather industry, as a pH regulator in processes such as the manufacture of cleaning agents, as a pelletizing agent in disinfectant pills for drinking water, as an additive in flue gas sulphation, in dishwasher tablets.

Adipic Acid is used as an additive in coating and chemicals.
Adipic Acid is used as an acidulant in dry powdered food mixtures, especially in those products having delicate flavors & where addition of a tang to the flavor is undesirable.

Adipic acid addition to foods imparts a smooth, tart taste.
In grape-flavored products, Adipic Acid adds a lingering supplementary flavor and gives an excellent set to food powders containing gelatin.

For concentrations of adipic acid ranging from 0.5-2.4 g/100 mL, the pH varies less than half a unit.
pH is low enough to inhibit browning of most fruits and other foodstuffs.

Adipic acid can be used as a starting material in the preparation of:
Aliphatic polyesters by reacting with ethyleneglycol/1,3 propyleneglycol/1,4-butanediol using inorganic acid as a catalyst.
Cyclopentanone using a weak base such as Na2CO3.
Linear polybutylene adipate (PBA) having carboxylic acids at the terminals by reacting with 1,4-butanediol.

Uses of Adipic Acid:
More than 92% of the production of Adipic acid is dedicated for the production of nylon 6,6 by a reaction with HMD Hexamethylene diamine.
Adipic Acid is used in nylon is utilized in fibbers, clothing, plastics, filaments, food packaging.

Adipic acid is also used in polyurethane resins, foam, shoe soles, and as food additive.
Esters of Adipic acid are used as plasticizers for PVC (Polyvinyl Chloride) resins and lubricant component.

Adipic acid is one of the largest chemical distributor in Europe.
Adipic acid is handling the storage, transport, export & import formalities of Adipic Acid globally.

About 60% of the 2.5 billion kg of adipic acid produced annually is used as monomer for the production of nylon by a polycondensation reaction with hexamethylene diamine forming nylon 66.
Other major applications also involve polymers; Adipic Acid is a monomer for production of polyurethane and Adipic Acid esters are plasticizers, especially in PVC.

In medicine:
Adipic acid has been incorporated into controlled-release formulation matrix tablets to obtain pH-independent release for both weakly basic and weakly acidic drugs.
Adipic Acid has also been incorporated into the polymeric coating of hydrophilic monolithic systems to modulate the intragel pH, resulting in zero-order release of a hydrophilic drug.

The disintegration at intestinal pH of the enteric polymer shellac has been reported to improve when adipic acid was used as a pore-forming agent without affecting release in the acidic media.
Other controlled-release formulations have included adipic acid with the intention of obtaining a late-burst release profile.

In foods:
Small but significant amounts of adipic acid are used as a food ingredient as a flavorant and gelling aid.
Adipic Acid is used in some calcium carbonate antacids to make them tart.

As an acidulant in baking powders, Adipic Acid avoids the undesirable hygroscopic properties of tartaric acid.
Adipic acid, rare in nature, does occur naturally in beets, but this is not an economical source for commerce compared to industrial synthesis.

Other Uses of Adipic Acid:
Alcoholic beverages,
Baked goods,
Condiments,
Relishes,
Fats,
Oils,
Gelatins,
Pudding,
Gravies,
Imitation dairy,
Instant coffee,
Tea,
Meat products,
Nonalcoholic beverages,
Poultry,
Snack foods,
Adhesives and Sealants,
Alkyd resins,
Beamhouse,
Carrier for fragances,
Coal,
Crop Protection,
Environment protection,
Gas desulphurization,
Hardener and crosslinking agents for polymeres,
Manufacturing of coating,
Manufacturing of dyestuffs,
Manufacturing of fibres,
Manufacturing of herbicides,
Manufacturing of pharmaceutical agents,
Manufacturing of photochemicals,
Manufacturing of plastics,
Manufacturing of tensides,
Manufacturing of textile dyestuffs,
Manufacturing of textiles dyestuffs,
Paper Manufacture,
Plasticizers for polymeres,
Polyester,
Polyester resins,
Polymer auxiliaries,
Soaking,
Synthetic lubricants,
Textile dyestuffs.

Production of Adipic Acid:
Adipic acid is white, crystalline compound mainly obtained by oxidation of cyclohexanol and cyclohexanone with nitric acid.
An alternative method of production of adipic acid is the hydrocarbonylation of butadiene, oxidation cleavage of cyclohexene.

Manufacturing Methods of Adipic Acid:
Commercially important processes employ two major reaction stages.
The first reaction stage is the production of the intermediates cyclohexanone and cyclohexanol, usually abbreviated as KA, KA oil, ol-one, or anone-anol.
The KA (ketone, alcohol), after separation from unreacted cyclohexane (which is recycled) and reaction by-products, is then converted to adipic acid by oxidation with nitric acid.

Cyclohexane is produced by the oxidation of cyclohexanol or cyclohexanone with air or nitric acid.

Preparation and Reactivity of Adipic Acid:
Adipic acid is produced from a mixture of cyclohexanone and cyclohexanol called KA oil, the abbreviation of ketone-alcohol oil.
The KA oil is oxidized with nitric acid to give adipic acid, via a multistep pathway.

Early in the reaction, the cyclohexanol is converted to the ketone, releasing nitrous acid:
HOC6H11 + HNO3 → OC(CH2)5 + HNO2 + H2O

Among Adipic Acid many reactions, the cyclohexanone is nitrosated, setting the stage for the scission of the C-C bond:
HNO2 + HNO3 → NO+NO3− + H2O
OC6H10 + NO+ → OC6H9-2-NO + H+

Side products of the method include glutaric and succinic acids.
Nitrous oxide is produced in about one to one mole ratio to the adipic acid, as well, via the intermediacy of a nitrolic acid.

Related processes start from cyclohexanol, which is obtained from the hydrogenation of phenol.

Alternative methods of production:
Several methods have been developed by carbonylation of butadiene.

For example, the hydrocarboxylation proceeds as follows:
CH2=CH−CH=CH2 + 2 CO + 2 H2O → HO2C(CH2)4CO2H

Another method is oxidative cleavage of cyclohexene using hydrogen peroxide.
The waste product is water.

Historically, adipic acid was prepared by oxidation of various fats, thus the name (ultimately from Latin adeps, adipis – "animal fat"; cf. adipose tissue).

Reactions:
Adipic acid is a dibasic acid (Adipic Acid has two acidic groups).
The pKa values for their successive deprotonations are 4.41 and 5.41.

With the carboxylate groups separated by four methylene groups, adipic acid is suited for intramolecular condensation reactions.
Upon treatment with barium hydroxide at elevated temperatures, Adipic Acid undergoes ketonization to give cyclopentanone.

Environmental of Adipic Acid:
The production of adipic acid is linked to emissions of N2O, a potent greenhouse gas and cause of stratospheric ozone depletion.

At adipic acid producers DuPont and Rhodia (now Invista and Solvay, respectively), processes have been implemented to catalytically convert the nitrous oxide to innocuous products:
2 N2O → 2 N2 + O2

Adipate salts and esters:
The anionic (HO2C(CH2)4CO2−) and dianionic (−O2C(CH2)4CO2−) forms of adipic acid are referred to as adipates.
An adipate compound is a carboxylate salt or ester of the acid.

Some adipate salts are used as acidity regulators, including:
Sodium adipate (E number E356)
Potassium adipate (E357)

Some adipate esters are used as plasticizers, including:
Bis(2-ethylhexyl) adipate
Dioctyl adipate
Dimethyl adipate

Human Metabolite Information of Adipic Acid:

Tissue Locations:
Kidney
Liver

Handling and Storage of Adipic Acid:

Nonfire Spill Response:
Do not touch or walk through spilled material.
Stop leak if you can do Adipic Acid without risk.

Prevent dust cloud.
For Asbestos, avoid inhalation of dust.

Cover spill with plastic sheet or tarp to minimize spreading.
Do not clean up or dispose of, except under supervision of a specialist.

SMALL DRY SPILL:
With clean shovel, place material into clean, dry container and cover loosely.
Move containers from spill area.

SMALL SPILL:
Pick up with sand or other non-combustible absorbent material and place into containers for later disposal.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Cover powder spill with plastic sheet or tarp to minimize spreading.
Prevent entry into waterways, sewers, basements or confined areas.

Storage Conditions of Adipic Acid:

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.

Storage class (TRGS 510):
Non Combustible Solids.

Safety of Adipic Acid:
Adipic acid, like most carboxylic acids, is a mild skin irritant.
Adipic Acid is mildly toxic, with a median lethal dose of 3600 mg/kg for oral ingestion by rats.

First Aid Measures of Adipic Acid:

General notes:
Take off contaminated clothing.

Following inhalation:
Provide fresh air.
In all cases of doubt, or when symptoms persist, seek medical advice.

Following skin contact:
Rinse skin with water/shower.
In all cases of doubt, or when symptoms persist, seek medical advice.

Following eye contact:
Irrigate copiously with clean, fresh water for at least 10 minutes, holding the eyelids apart.
In case of eye irritation consult an ophthalmologist.

Following ingestion:
Rinse mouth.
Call a doctor if you feel unwell.

INHALATION:
Remove victim to fresh air.
Get medical attention if irritation persists.

EYES:
Flush with water for at least 15 min.

SKIN:
Flush with water.

Fire Fighting of Adipic Acid:

SMALL FIRE:
Dry chemical, CO2, water spray or regular foam.

LARGE FIRE:
Water spray, fog or regular foam.
Do not scatter spilled material with high-pressure water streams.

If Adipic Acid can be done safely, move undamaged containers away from the area around the fire.
Dike runoff from fire control for later disposal.

FIRE INVOLVING TANKS:
Cool containers with flooding quantities of water until well after fire is out.
Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

Fire Fighting Procedures of Adipic Acid:

Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Wear self-contained breathing apparatus for firefighting if necessary.

Stop discharge if possible, keep people away.
Shut off ignition sources.

Call fire department.
Avoid contact with solid and dust.
Isolate and remove discharged material.

If material on fire or involved in fire:
Use water in flooding quantities as fog.
Solid streams of water may spread fire.

Cool all affected containers with flooding quantities of water.
Apply water from as far a distance as possible.
Use foam, dry chemical, or carbon dioxide.

Accidental Release Measures of Adipic Acid:

Isolation and Evacuation:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.

SPILL:
Increase the immediate precautionary measure distance, in the downwind direction, as necessary.

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions.
Also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Spillage Disposal of Adipic Acid:
Sweep spilled substance into covered plastic containers.
If appropriate, moisten first to prevent dusting.
Wash away remainder with plenty of water.

Cleanup Methods of Adipic Acid:

Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
Avoid dust formation.

Avoid breathing vapors, mist or gas.
Ensure adequate ventilation.

Evacuate personnel to safe areas.
Avoid breathing dust.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Pick up and arrange disposal without creating dust.
Sweep up and shovel.
Keep in suitable, closed containers for disposal.

Environmental considerations- land spill:
Dig a pit, pond, lagoon, or holding area to contain liquid or solid material.
If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner.
Cover solids with a plastic sheet to prevent dissolving in rain or fire fighting water.

Environmental considerations- water spill:
Use natural deep water pockets, excavated lagoons, or sand bag barriers to trap material at bottom.
If dissolved, in region of 10 ppm or greater concentration, apply activated carbon at ten times the spilled amount.

Remove trapped material with suction hoses.
Use mechanical dredges or lifts to remove immobilized masses of pollutants and precipitates.

Electrochemical measurements have been made on the system Cu(2+), adipic acid, nitric acid (which models the effluent from adipic acid plants) to investigate the reasons for the observed low current efficiency for copper deposition from such soln.
The most probable cause is a cathodic shift in the deposition potential of copper making the reduction of NO3- the preferred process.

Depletion experiments have been carried out on real effluent in two three-dimensional cells, a bipolar trickle tower and a porous reticulated carbon bed.
Each performs reasonably well and, while the current efficiencies are low (about 20%), the deposition is essentially mass-transfer controlled.

Neutralizing agents for acids and caustics:
Rinse with dilute soda ash solution.

Identifiers of Adipic Acid:
CAS Number: 124-04-9
Beilstein Reference: 1209788
ChEBI: CHEBI:30832
ChEMBL: ChEMBL1157
ChemSpider: 191
ECHA InfoCard: 100.004.250
EC Number: 204-673-3
E number: E355 (antioxidants, ...)
Gmelin Reference: 3166
KEGG: D08839
PubChem CID: 196
RTECS number: AU8400000
UNII: 76A0JE0FKJ
UN number: 3077
CompTox Dashboard (EPA): DTXSID7021605

InChI:
InChI=1S/C6H10O4/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H,7,8)(H,9,10)
Key: WNLRTRBMVRJNCN-UHFFFAOYSA-N
InChI=1/C6H10O4/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H,7,8)(H,9,10)
Key: WNLRTRBMVRJNCN-UHFFFAOYAY

SMILES:
O=C(O)CCCCC(=O)O
C(CCC(=O)O)CC(=O)O

CAS number: 124-04-9
EC index number: 607-144-00-9
EC number: 204-673-3
Hill Formula: C₆H₁₀O₄
Molar Mass: 146.14 g/mol
HS Code: 2917 12 00

CAS Number: 124-04-9
Molecular Weight: 146.14
Beilstein: 1209788
EC Number: 204-673-3
MDL number: MFCD00004420
eCl@ss: 39021711
PubChem Substance ID: 57653836
NACRES: NA.21

CAS: 124-04-9
Molecular Formula: C6H10O4
Molecular Weight (g/mol): 146.142
MDL Number: MFCD00004420
InChI Key: WNLRTRBMVRJNCN-UHFFFAOYSA-N
PubChem CID: 196
ChEBI: CHEBI:30832
IUPAC Name: hexanedioic acid
SMILES: C(CCC(=O)O)CC(=O)O

Properties of Adipic Acid:
Chemical formula: C6H10O4
Molar mass: 146.142 g·mol−1
Appearance: White crystals[1]
Monoclinic prisms[2]
Odor: Odorless
Density: 1.360 g/cm3
Melting point: 152.1 °C (305.8 °F; 425.2 K)
Boiling point: 337.5 °C (639.5 °F; 610.6 K)
Solubility in water: 14 g/L (10 °C)
24 g/L (25 °C)
1600 g/L (100 °C)
Solubility: Very soluble in methanol, ethanol
soluble in acetone, acetic acid
slightly soluble in cyclohexane
negligible in benzene, petroleum ether
log P: 0.08
Vapor pressure: 0.097 hPa (18.5 °C) = 0.073 mmHg
Acidity (pKa): 4.43, 5.41
Conjugate base: Adipate
Viscosity: 4.54 cP (160 °C)

Density: 1.36 g/cm3 (25 °C)
Flash point: 196 °C
Ignition temperature: 405 °C
Melting Point: 150.85 °C
pH value: 2.7 (23 g/l, H₂O, 25 °C)
Vapor pressure: 0.097 hPa (18.5 °C)
Bulk density: 700 kg/m3
Solubility: 15 g/l

General Properties: White, solid crystals
Odor: Odorless
Intensity: 1.360 g/cm3
Boiling point: 337,5°C
Melting point: 152,1 °C
Flash point: 196°C
Vapor pressure: 0,0073 mmHg (18,5 °C)
Refraction index: –
Solubility (aquenous): 14g/L (10°C), 1600 g/L (100°C)

Vapor density: 5 (vs air)
Quality Level: 200
Vapor pressure: 1 mmHg ( 159.5 °C)
Assay: 99%
Form: crystals
Autoignition temp.: 788 °F
bp: 265 °C/100 mmHg (lit.)
mp: 151-154 °C (lit.)
Solubility: H2O: soluble 23 g/L at 25 °C
SMILES string: OC(=O)CCCCC(O)=O
InChI: 1S/C6H10O4/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H,7,8)(H,9,10)
InChI key: WNLRTRBMVRJNCN-UHFFFAOYSA-N

Molecular Weight: 146.14
XLogP3: 0.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 5
Exact Mass: 146.05790880
Monoisotopic Mass: 146.05790880
Topological Polar Surface Area: 74.6 Ų
Heavy Atom Count: 10
Complexity: 114
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Adipic Acid:
Assay (acidimetric): ≥ 99.0 %
Melting range (lower value): ≥ 150 °C
Melting range (upper value): ≤ 154 °C
Identity (IR): passes test

Melting Point: 151.0°C to 153.0°C
Boiling Point: 337.0°C
CAS Min %: 98.5
CAS Max %: 100.0
Color: White
Assay Percent Range: 99%
Linear Formula: HO2C(CH2)4CO2H
Beilstein: 02, 649
Fieser: 01,15
Merck Index: 15, 150
Formula Weight: 146.14
Percent Purity: 99%
Quantity: 500 g
Flash Point: 196°C
Infrared Spectrum: Authentic
Packaging: Plastic bottle
Physical Form: Crystalline Powder
Chemical Name or Material: Adipic acid

Structure of Adipic Acid:
Crystal structure: Monoclinic

Thermochemistry of Adipic Acid:
Std enthalpy of formation (ΔfH⦵298): −994.3 kJ/mol[3

Related Products of Adipic Acid:
Hydroxynorketamine-d6 Hydrochloride
(S)-Ketamine-d6 Hydrochloride
Norketamine-d4
S-(-)-Norketamine-d6 Hydrochloride
Phencyclidine-d5 Hydrochloride

Related compounds of Adipic Acid:

Related dicarboxylic acids:
glutaric acid
pimelic acid

Related compounds:
hexanoic acid
adipic acid dihydrazide
hexanedioyl dichloride
hexanedinitrile
hexanediamide

Names of Adipic Acid:

Preferred IUPAC name:
Hexanedioic acid

Other names:
Adipic acid
Butane-1,4-dicarboxylic acid
Hexane-1,6-dioic acid
1,4-butanedicarboxylic acid

Synonyms of Adipic Acid:
adipic acid
hexanedioic acid
124-04-9
Adipinic acid
1,4-Butanedicarboxylic acid
Adilactetten
Acifloctin
Acinetten
1,6-Hexanedioic acid
Molten adipic acid
Kyselina adipova
Adipinsaure [German]
Acide adipique [French]
FEMA No. 2011
Kyselina adipova [Czech]
Hexanedioate
Adipinsaeure
adipic-acid
Adipidic acid
Adi-pure
NSC 7622
Adipic acid [NF]
NSC-7622
Hexan-1,6-dicarboxylate
76A0JE0FKJ
Hexanedioc acid
INS NO.355
1,6-HEXANE-DIOIC ACID
E-355
CHEBI:30832
INS-355
NSC7622
Adipic acid (NF)
NCGC00091345-01
E355
hexane-1,6-dioic acid
Adipinsaure
Acide adipique
FEMA Number 2011
CAS-124-04-9
CCRIS 812
HSDB 188
EINECS 204-673-3
MFCD00004420
UNII-76A0JE0FKJ
BRN 1209788
Adipinate
Molten adipate
AI3-03700
hexane dioic acid
1,6-Hexanedioate
0L1
Adipic acid, 99%
Neopentyl Glycol Flake
Adipic acid-[13C6]
1, 6-Hexanedioic Acid
Adipic acid, >=99%
ADIPIC ACID [II]
ADIPIC ACID [MI]
WLN: QV4VQ
ADIPIC ACID [FCC]
bmse000424
EC 204-673-3
ADIPIC ACID [FHFI]
ADIPIC ACID [HSDB]
ADIPIC ACID [INCI]
SCHEMBL4930
CHEMBL1157
NCIOpen2_001004
NCIOpen2_001222
HOOC-(CH2)4-COOH
ADIPIC ACID [MART.]
Adipic acid, >=99.5%
4-02-00-01956 (Beilstein Handbook Reference)
ADIPIC ACID [USP-RS]
ADIPIC ACID [WHO-DD]
BIDD:ER0342
INS No. 355
DTXSID7021605
Adipic acid, puriss., 99.8%
Pharmakon1600-01301012
ADIPIC ACID [EP MONOGRAPH]
ZINC1530348
Tox21_111118
Tox21_202161
Tox21_300344
BBL011615
LMFA01170048
NSC760121
s3594
STL163338
AKOS000119031
Tox21_111118_1
CCG-230896
CS-W018238
HY-W017522
NSC-760121
NCGC00091345-02
NCGC00091345-03
NCGC00091345-04
NCGC00091345-05
NCGC00254389-01
NCGC00259710-01
AC-10343
BP-21150
BP-30248
Hexanedioic Acid, Butanedicarboxylic Acid
A0161
Adipic acid, BioXtra, >=99.5% (HPLC)
Adipic acid, SAJ special grade, >=99.5%
E 355
FT-0606810
EN300-18041
Adipic acid, Vetec(TM) reagent grade, >=99%
C06104
D08839
D70505
AB00988898-01
AB00988898-03
Q357415
SR-01000944270
J-005034
J-519542
SR-01000944270-2
Z57127533
Adipic acid, certified reference material, TraceCERT(R)
F0001-0377
Adipic acid, European Pharmacopoeia (EP) Reference Standard
1F1316F2-7A32-4339-8C2A-8CAA84696C95
Adipic acid, United States Pharmacopeia (USP) Reference Standard
124-04-9 [RN]
204-673-3 [EINECS]
Acide adipique [French] [ACD/IUPAC Name]
Adipic acid [ACD/IUPAC Name] [Wiki]
Adipinsäure [German] [ACD/IUPAC Name]
Asapic
Hexanedioic acid [ACD/Index Name]
Inipol DS
kwas adypinowy [Polish]
kyselina adipová [Czech]
MFCD00004420 [MDL number]
1,4-butanedicarboxylic acid
1,6-HEXANEDIOIC ACID
1,6-HEXANE-DIOIC ACID
121311-78-2 [RN]
19031-55-1 [RN]
2-Oxoadipic acid
52089-65-3 [RN]
Acifloctin
Acinetten
Adilactetten
Adipic Acid FCC
adipicacid
adipinic acid
Butane-1,4-dicarboxylic acid
BUTANEDICARBOXYLIC ACID
Hexanedioic-3,3,4,4-d4 Acid
hydron [Wiki]
QV4VQ [WLN]
ADIPIC ACID DIHYDRAZIDE
DISTARCH PHOSPHATE ACETATE N° CAS : 68130-14-3 - Adipate de diamidon acétylé Nom INCI : DISTARCH PHOSPHATE ACETATE Additif alimentaire : E1422 Agent stabilisant : Améliore les ingrédients ou la stabilité de la formulation et la durée de conservation Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
ADIPIC DIHYDRAZIDE
Adipic Dihydrazide is a chemical used for cross-linking water-based emulsions.
Adipic Dihydrazide is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.


CAS Number: 1071-93-8
EC Number: 213-999-5
MDL number: MFCD00007614
Linear Formula: NH2NHCO(CH2)4CONHNH2
Molecular Formula: C6H14N4O2


Adipic Dihydrazide is a latent hardener for epoxy resin.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).


Adipic Dihydrazide is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Adipic Dihydrazide is an effective crosslinking agent, curative and hardener.


Adipic Dihydrazide is the most common dihydrazide crosslinking agent within a series of dihydrazides such as sebacic dihydrazide (SDH) and isophthalic dihydrazide (IDH).
Adipic Dihydrazide’s has a melting point of 180 °C and a molecular weight of 174; both are lower than the alternative dihydrazides SDH and IDH.


Adipic Dihydrazide is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).


The applications of Adipic Dihydrazide are facilitated by the nucleophilicity of the amine function (good reaction characteristics), the good overall properties and weatherability of cured systems.
The moderate solubility of Adipic Dihydrazide in water (50 g./liter) and common organic solvents facilitates the use of Adipic Dihydrazide in aqueous and solvent based systems.


The cure temperature for epoxy resins (glycidyl types) formulated with Adipic Dihydrazide is influenced by the melt-out temperature of the ADH, which allows an extended pot life at low temperatures.
Storage stability can be up to six-months at room temperature, with cure times of about one-hour at 130 °C.


Cure rates can be accelerated using tin or titanate catalysts, or imidazoles.
One-component Adipic Dihydrazide epoxy systems can be partially cured or “B-staged”, and later fully cured.
B-staging provides handling, processing, and fabrication advantages.



USES and APPLICATIONS of ADIPIC DIHYDRAZIDE:
Adipic Dihydrazide is used to functionalize magnetic nanoparticles for glycopeptide enrichment and identification.
Adipic Acid Dihydrazide can also be used as a chain extension for liquid rubber.
Adipic Dihydrazide can also be used as a hardener for certain epoxy resins.


Adipic Dihydrazide is used adhesives and sealant chemicals, and Automotive care products.
Adipic Dihydrazide is used for epoxy powder coating curing agent and coating additives, Metal deactivator and other polymer additives and water treatment agent.


Adipic Dihydrazide is the most suitable hydrazide crosslinking agent.
Adipic Dihydrazide and diacetone acrylamide have been widely used in water-based paint emulsion.
Adipic Dihydrazide is weakly alkaline, solid ADH is directly added to the emulsion may produce coalescence, usually ADH should be dissolved in hot water (poor solubility in cold water) and reused.


Adipic Dihydrazide bifunctional compound, which can be cross-linked with sodium hyaluronate as a protein drug carrier.
Adipic Dihydrazide plays a cross-linking role with diacetone acrylamide in the post-crosslinking of water emulsion and water-soluble polymer, such as water-based coatings, adhesives, fibers, plastic film treatment, hair spray, etc., and can also be used as epoxy powder coating curing agent And water-based coating additives, metal deactivators and other polymer additives and water treatment agents, indoor formaldehyde adsorbents and intermediate raw materials.


The same type of bifunctional linker for aldehydes can produce relatively stable hydrazone linkage; for the linkage of carbohydrate proteins, such as antibodies, periodate oxidation reaction occurs at a specific form of position; at pH 5.0, oxidation reaction and coupling reaction can be carried out conveniently, hydrazide derived from low pKa value can avoid competitive reaction through primary amine.


Adipic Dihydrazide is mainly used for epoxy powder coating curing agent and coating additives, metal deactivator and other polymer additives and water treatment agents.
Adipic Dihydrazide is used as a crosslinking agent in acrylic emulsion with ketone group.


Adipic Dihydrazide is used in epoxy adhesives and sealants.
Adipic Dihydrazide is used crosslinking agent for self crosslinking emulsion resins using DAAM.
Adipic Dihydrazide, also known as ADH or Adipohydrazide, can be used as a hardener for epoxy resins and for cross-linking water-based emulsions.


Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
Adipic Dihydrazide is used analytical Reagents, Diagnostic Reagents, Teaching Reagents.


Adipic Dihydrazide is used for Biological Purpose, For Tissue Medium Purpose, For Electron Microscopy, For Lens Blooming, Pro Analysis, Super Special Grade, For Scintillation, For Electrophoresis Use, For Refractive Index.
Adipic Dihydrazide is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Adipic Dihydrazide is used in the following products: coating products, adhesives and sealants, fillers, putties, plasters, modelling clay, finger paints, polymers, non-metal-surface treatment products, textile treatment products and dyes and washing & cleaning products.
The same bifunctional crosslinking reagent, Adipic Dihydrazide, is specially used for aldehydes to generate relatively stable hydrazone links.


Other release to the environment of Adipic Dihydrazide is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).


Other release to the environment of Adipic Dihydrazide is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Adipic Dihydrazide can be found in complex articles, with no release intended: vehicles covered by End of Life Vehicles (ELV) directive (e.g. personal vehicles or delivery vans).
In particular, Adipic Dihydrazide is used to connect glycoproteins, such as antibodies.


Adipic Dihydrazide is used in the following products: adhesives and sealants, coating products, paper chemicals and dyes, textile treatment products and dyes and washing & cleaning products.
Adipic Dihydrazide is used for the manufacture of: textile, leather or fur and wood and wood products.


Other release to the environment of Adipic Dihydrazide is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).


Adipic Dihydrazide is used in the following products: adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, polymers, textile treatment products and dyes and finger paints.
Release to the environment of Adipic Dihydrazide can occur from industrial use: formulation of mixtures and formulation in materials.


Adipic Dihydrazide is used in the following products: paper chemicals and dyes, coating products, textile treatment products and dyes, adhesives and sealants, finger paints, laboratory chemicals, washing & cleaning products and water treatment chemicals.
Adipic Dihydrazide is used for the manufacture of: chemicals, pulp, paper and paper products and plastic products.


Release to the environment of Adipic Dihydrazide can occur from industrial use: for thermoplastic manufacture, as an intermediate step in further manufacturing of another substance (use of intermediates), in the production of articles and as processing aid.
Release to the environment of Adipic Dihydrazide can occur from industrial use: manufacturing of the substance.


Adipic Dihydrazide is a homobifunctional cross-linking reagent specific for aldehydes resulting in relatively stable hydrazone linkages.
Adipic Dihydrazide is typically, used in the linking of glycoproteins, such as antibodies, in a site-specific fashion following periodate oxidation.
Oxidation and coupling may conveniently be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.


Adipic Dihydrazide is used to functionalize magnetic nanoparticles for gylcopeptitde enrichment and identification.
Adipic Dihydrazide can also be used as a chain extension for liquid rubber.
Adipic Dihydrazide is used for synthesis.


Adipic Dihydrazide is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.
Adipic Dihydrazide is also employed as a paint additive and coating additive.
Adipic Dihydrazide is also used as an intermediate.


Further, Adipic Dihydrazide is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.
Adipic Dihydrazide is widely used as cross-linker in waterborne acrylic emulsions.


Adipic Dihydrazide is added to the water phase in a PUD.
Crosslinking occurs during the drying and film coalescence process which is ideal for maximizing the film properties including gloss, scrub, stain and wear resistance and durability.


Other crosslinking methods where crosslinking occurs prior to film coalescence exhibit reduced performance properties including poor flow and leveling.
The full reactivity characteristics of Adipic Dihydrazide are ideal for PUR systems.
Alternative curatives which show incomplete crosslinking due to slow reactivity and the lack of curative mobility in a dry film will also compromise performance.


The DAAM/Adipic Dihydrazide pair is also used in crosslinkable sizing agents, thickeners, adhesives, and sealants.
Adipic Dihydrazide is a unique crosslinking agent and curative, offering controlled reactivity and performance enhancements in epoxy resins, polyurethane dispersions (PUDs), solvent based PURs and emulsion acrylic resins.


The major applications for Adipic Dihydrazide are a latent curing agent for B-stageable epoxy resins and an ambient temperature crosslinking agent for high performance acrylic emulsion architectural coatings.
Systems crosslinked or cured with Adipic Dihydrazide exhibit good color stability and weathering characteristics, adhesion, durability, hardness, and toughness.


Adipic Dihydrazide is a chemical used for cross-linking water-based emulsions.
Adipic Dihydrazide can also be used as a hardener for certain epoxy resins.
Adipic Dihydrazide is used as a difunctional crosslinking agent in paints and coatings for certain water-based acrylic emulsions.


Adipic Dihydrazide is used as a hardener for epoxy resins and a chain extender for polyurethanes.
A small use is as a formaldehyde scavenger preventing the liberation of formaldehyde.
One component epoxy resins are used in coatings such as powder coatings, adhesives including hot melt adhesives, molding compounds and in fiber reinforced composites.


Glass and carbon fiber prepreg obtained by a hot melt impregnation method are used in the fabrication of sporting goods, wind turbine blades and aircraft/aerospace components.
With Adipic Dihydrazide cure, epoxy resins exhibit excellent toughness, flexibility, and adhesive properties.


Tg’s of 140-160 °C are achievable using a standard liquid bisphenol A epoxy resin (DGEBA) with Adipic Dihydrazide as the hardener.
Rigid and flexible epoxy adhesives have been formulated as one component systems that can be stored at room temperature using ADH as a latent curing agent.
Rigid epoxy adhesives are based on bisphenol A and novolac epoxides.


These rigid adhesives exhibit excellent cohesive and adhesive properties to a wide variety of surfaces.
Flexible epoxy adhesives produce more pliable bonds which better accommodate bond line stresses or differential substrate expansion rates.
Flexible epoxy resins include aliphatic di- and tri-epoxy resins such as hexanediol diglycidyl ether and poly(oxypropylene) diglycidyl ethers.
Semi-rigid epoxy-based adhesives utilize mixtures of both classes of epoxy resins or rigid formulations using flexibilizers.


-Epoxy Resins:
A notable fact with regard to Adipic Dihydrazide in epoxy formulations is that each of the primary amine end groups has a functionality of two, so the Adipic Dihydrazide molecule has an equivalency of four per epoxy moiety.
Accordingly, the active hydrogen equivalent weight of Adipic Dihydrazide is 43.5.
When formulated with epoxy resins, the Adipic Dihydrazide index can range between 0.85-1.15 of stoichiometric proportions, without a significant effect on mechanical properties.



PHYSICAL AND CHEMICAL PROPERTIES OF ADIPIC DIHYDRAZIDE:
*physical and chemical properties appearance white crystalline powder
*soluble in water, slightly soluble in acetone, and acetic anhydride or acid chloride can occur acylation reaction, is an important amide hydrazine compounds.



POLYURETHANE DISPERSIONS (PUDs):
Adipic Dihydrazideis an effective room temperature curative for aqueous PUDs and solution polyurethanes.
In this capacity, Adipic Dihydrazide provides polyurea coatings with higher hardness, toughness and adhesion properties, excellent mechanical properties, abrasion and chemical resistance.
Adipic Dihydrazide cured polyurethane coatings exhibit good color stability and weathering properties, which is not observed with standard amine curatives.



PHYSICAL and CHEMICAL PROPERTIES of ADIPIC DIHYDRAZIDE:
Molecular Weight: 174.20 g/mol
XLogP3-AA: -2.1
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 5
Exact Mass: 174.11167570 g/mol
Monoisotopic Mass: 174.11167570 g/mol
Topological Polar Surface Area: 110Ų
Heavy Atom Count: 12
Formal Charge: 0
Complexity: 142
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Physical state: powder
Color: white
Odor: No data available
Melting point/freezing point
Melting point/range: 180 - 182 °C - lit.
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 150 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 102 g/l at 20 °C - soluble
Partition coefficient:
n-octanol/water:
log Pow: -2,7 at 20 °C

Vapor pressure: No data available
Density: No data available
Relative density: 1,29 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available
Molecular Formula: C6H14N4O2
Molar Mass: 174.2
Density: 1.186g/cm3
Melting Point: 175-182℃
Boling Point: 519.3°C at 760 mmHg
Flash Point: 267.9°C
Water Solubility: soluble
Vapor Presure: 6.92E-11mmHg at 25°C
Appearance: White crystal

Storage Condition: 2-8℃
Sensitive: Sensitive to air
Refractive Index: 1.513
MDL: MFCD00007614
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 519.30 °C. @ 760.00 mm Hg (est)
Flash Point: 514.00 °F. TCC ( 267.90 °C. ) (est)
logP (o/w): -2.670 (est)
Soluble in: water, 3.287e+005 mg/L @ 25 °C (est)
Appearance (Colour): White to pale yellow
Appearance (Form): Powder
Solubility: (Turbidity) 10% aq. solution: Clear
Solubility: (Colour) 10% aq. solution: Colourless to pale yellow
Assay (NT): min. 95.0%
Melting Point: 178 - 182°C
Loss on drying: max. 0.5%

CAS number: 1071-93-8
EC number: 213-999-5
Hill Formula: C₆H₁₄N₄O₂
Molar Mass: 174.2 g/mol
HS Code: 2928 00 90
Flash point: 150 °C
Ignition temperature: 360 °C
Melting Point: 180 - 182 °C
Melting Point: 178.0°C to 182.0°C
Color: White to Yellow
Infrared Spectrum: Authentic
Assay Percent Range: 8%
Linear Formula: H2NNHCO(CH2)4CONHNH2
Beilstein: 02, I, 277
Solubility Information Solubility in water: soluble.
Other solubilities: soluble in acetic acid,slightly soluble in acetone,
insoluble in ethanol,ether and benzene
Formula Weight: 174.2
Percent Purity: 98%
Physical Form: Crystalline Powder

Molecular Weight:174.20100
Exact Mass:174.20
EC Number:213-999-5
UNII:VK98I9YW5M
NSC Number:29542|3378
DSSTox ID:DTXSID0044361
HScode:2928000090
PSA:110.24000
XLogP3:-2.1
Appearance:DryPowder
Density:1.186 g/cm3
Melting Point:171 °C @ Solvent: Water
Boiling Point:519.3ºC at 760 mmHg
Flash Point:> 109ºC
Refractive Index:1.513
Water Solubility:H2O: soluble
Storage Conditions: -20ºC

Vapor Pressure: 6.92E-11mmHg at 25°C
Molecular Weight: 174.20
XLogP3:-2.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:174.11167570
Monoisotopic Mass:174.11167570
Topological Polar Surface Area:110
Heavy Atom Count:12
Complexity:142
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes



FIRST AID MEASURES of ADIPIC DIHYDRAZIDE:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of ADIPIC DIHYDRAZIDE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of ADIPIC DIHYDRAZIDE:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of ADIPIC DIHYDRAZIDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses.
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ADIPIC DIHYDRAZIDE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
*Storage stability:
Recommended storage temperature:
-20 °C



STABILITY and REACTIVITY of ADIPIC DIHYDRAZIDE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .



SYNONYMS:
Hexanedihydrazide
Adipic dihydrazide
1071-93-8
Adipic acid dihydrazide
Adipohydrazide
Hexanedihydrazide
Hexanedioic acid, dihydrazide
Adipyl hydrazide
Hexanediohydrazide
Adipic acid, dihydrazide
Adipoyldihydrazine
adipoyl dihydrazide
VK98I9YW5M
DTXSID0044361
Hexanedioic acid, 1,6-dihydrazide
NSC 3378
NSC-3378
EINECS 213-999-5
NSC 29542
NSC-29542
AI3-22640
WLN: ZMV4VMZ
EC 213-999-5
MFCD00007614
Adipodihydrazide
Adip dihydr
adipic hydrazide
Adipoyl hydrazide
adipic dihydrazone
Hexanedihydrazide #
Adipic aciddihydrazide
Adipic acid dihyrazide
Hexanedioic dihydrazide
AJICURE ADH
QUALIMER ADH
ULTRALINK HYDRAZIDE
Hexanedioic acid dihydrazide
SCHEMBL49856
Adipic Acid Dihydrazide (ADH)
CHEMBL3185968
DTXCID8024361
SCHEMBL11037942
AMY3771
NSC3378
1,4-Butanedicarboxylic dihydrazide
BK 1000Z
BT 1000Z
NSC29542
STR02658
Tox21_301067
BBL022965
STK709135
ADIPIC ACID DIHYDRAZIDE [INCI]
AKOS000267183
NCGC00248276-01
NCGC00257525-01
CAS-1071-93-8
A0170
Adipic acid dihydrazide, >=98% (titration)
CS-0010116
FT-0621914
EN300-03706
D72486
T 2210
Adipic acid dihydrazide, purum, >=97.0% (NT)
A801603
J-660023
Q-200600
Q4682936
Z56812730
F1943-0024
Hexanedihydrazide
Adipic dihydrazide
Adipohydrazide
Adipyl hydrazide
Adipic acid dihydrazide
Adipyl hydrazide
Adipic acid dihyrazide
Hexanedioic acid, dihydrazide
403
adipohydrazide
Hexanedioic Acid Dihydrazide
ADH
ADH (hydrazide)
ADH 4S
ADH-J
ADH-S
Adipic Dihydrazide
Adipoyl Dihydrazide
Adipoyl Hydrazide
Adipoyldihydrazine
Ajicure ADH
BK 1000Z
BT 1000Z
NSC 29542
NSC 3378
Qualimer ADH
T 2210
Adipohydrazide
adipic dihydrazide
adipohydrazide
adipic acid dihydrazide
hexanedioic acid
dihydrazide
adipyl hydrazide
hexanediohydrazide
adipic acid
dihydrazide, adipodihydrazide
hexanedioic acid
1,6-dihydrazide
unii-vk98i9yw5m
Hexanedioic acid,1,6-dihydrazide
Adipic acid dihydrazide
Hexanedioic acid,dihydrazide
Adipic dihydrazide
Adipoyl hydrazide
ADH
Adipoyl dihydrazide
Adipoyldihydrazine
Qualimer ADH
BT 1000Z
BK 1000Z
NSC 29542
NSC 3378
ADH 4S
ADH (hydrazide)
ADH-J
ADH-S
T 2210
Ajicure ADH
Adipic acid dihydrazide
Technicure ADH
Epicure PD 797
98152-55-7
124246-54-4
ADH
Adipohydrazide
ADIPODIHYDRAZIDE
adipoyl hydrazide
ADIPIC DIHYDRAZIDE
Adipic dihydrazide
ADIPINIC DIHYDRAZIDE
ADIPIC ACID DIHYDRIZIDE
ADIPIC ACID DIHYDRAZIDE
ADIPIC DIHYDRAZIDE (C6H14N4O2)
Adipic dihydrazide (C6H14N4O2) is a chemical used for cross-linking water-based emulsions.
Adipic dihydrazide (C6H14N4O2) can also be used as a hardener for certain epoxy resins.
Adipic dihydrazide (C6H14N4O2) is a symmetrical molecule with a C4 backbone, and the reactive group is C=ONHNH2.

CAS: 1071-93-8
MF: C6H14N4O2
MW: 174.2
EINECS: 213-999-5

Synonyms
ADH;ADIPINIC DIHYDRAZIDE;ADIPIC DIHYDRAZIDE;ADIPIC ACID DIHYDRAZIDE;ADIPIC ACID DIHYDRIZIDE;adipoyl hydrazide;ADIPODIHYDRAZIDE;Adipohydrazide;Adipic dihydrazide;1071-93-8;Adipic acid dihydrazide;Adipohydrazide;Hexanedihydrazide;Hexanedioic acid, dihydrazide;Adipic acid, dihydrazide;Adipoyldihydrazine;adipoyl dihydrazide;MFCD00007614;VK98I9YW5M;DTXSID0044361;Hexanedioic acid, 1,6-dihydrazide;NSC-3378;NSC-29542;WLN: ZMV4VMZ;Adipyl hydrazide;Adipodihydrazide;Adip dihydr;adipic hydrazide;Adipoyl hydrazide;adipic dihydrazone;Hexanedihydrazide #;NSC 3378;EINECS 213-999-5;NSC 29542;Adipic aciddihydrazide;Adipic acid dihyrazide;Hexanedioic dihydrazide;AJICURE ADH;QUALIMER ADH;AI3-22640;ULTRALINK HYDRAZIDE;UNII-VK98I9YW5M;EC 213-999-5;Hexanedioic acid dihydrazide;SCHEMBL49856;CHEMBL3185968;DTXCID8024361;SCHEMBL11037942;AMY3771;NSC3378;1,4-Butanedicarboxylic dihydrazide;BK 1000Z;BT 1000Z;NSC29542;STR02658;Tox21_301067;ADIPIC ACID DIHYDRAZIDE [INCI];AKOS000267183;NCGC00248276-01;NCGC00257525-01;CAS-1071-93-8;A0170;Adipic acid dihydrazide, >=98% (titration);CS-0010116;FT-0621914;NS00003709;EN300-03706;D72486;T 2210;Adipic acid dihydrazide, purum, >=97.0% (NT);A801603;J-660023;Q-200600;Q4682936;Z56812730;F1943-0024
;InChI=1/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12

Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).
Adipic dihydrazide (C6H14N4O2) is the most suitable hydrazide cross-linking agent, and ADH has been widely used in water-based paint emulsions in combination with diacetone acrylamide.
Adipic dihydrazide (C6H14N4O2) is weakly alkaline, and there is a possibility of agglomeration when solid ADH is added directly to the emulsion, so usually Adipic dihydrazide (C6H14N4O2) should be dissolved in hot water before use.
Adipic dihydrazide (C6H14N4O2) is an effective crosslinking agent, curative and hardener.
Adipic dihydrazide (C6H14N4O2) is the most common dihydrazide crosslinking agent within a series of dihydrazides such as sebacic dihydrazide (SDH) and isophthalic dihydrazide (IDH).
Adipic dihydrazide (C6H14N4O2)’s has a melting point of 180 °C and a molecular weight of 174; both are lower than the alternative dihydrazides SDH and IDH.

Adipic dihydrazide (C6H14N4O2) is used as a difunctional crosslinking agent in paints and coatings for certain water-based acrylic emulsions.
Adipic dihydrazide (C6H14N4O2) is used as a hardener for epoxy resins and a chain extender for polyurethanes.
A small use is as a formaldehyde scavenger preventing the liberation of formaldehyde.
Adipic dihydrazide (C6H14N4O2) is the most suitable hydrazide crosslinking agent.
Adipic dihydrazide (C6H14N4O2) and diacetone acrylamide have been widely used in water-based paint emulsion.
Adipic dihydrazide (C6H14N4O2) is weakly alkaline, solid ADH is directly added to the emulsion may produce coalescence, usually Adipic dihydrazide (C6H14N4O2) should be dissolved in hot water (poor solubility in cold water) and reused.

Adipic dihydrazide (C6H14N4O2) Chemical Properties
Melting point: 180-182 °C (lit.)
Boiling point: 305.18°C (rough estimate)
Density: 1.2297 (rough estimate)
Vapor pressure: 0Pa at 25℃
Refractive index: 1.6700 (estimate)
Fp: 150 °C
Storage temp.: -20°C
Solubility: H2O: 100 mg/mL
Pka: 12.93±0.35(Predicted)
Form: Crystalline Powder
Color: White to slightly yellow
Water Solubility: soluble
BRN: 973863
InChIKey: IBVAQQYNSHJXBV-UHFFFAOYSA-N
LogP: -2.7 at 20℃
CAS DataBase Reference: 1071-93-8(CAS DataBase Reference)
NIST Chemistry Reference: Adipic dihydrazide (C6H14N4O2) (1071-93-8)
EPA Substance Registry System: Adipic dihydrazide (C6H14N4O2) (1071-93-8)

Uses
Adipic dihydrazide (C6H14N4O2) is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.
Adipic dihydrazide (C6H14N4O2) is also employed as a paint additive and coating additive.
Adipic dihydrazide (C6H14N4O2) is also used as an intermediate.
Further, Adipic dihydrazide (C6H14N4O2) is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.
Adipic dihydrazide (C6H14N4O2) is a homobifunctional cross-linking reagent specific for aldehydes resulting in relatively stable hydrazone linkages.
Adipic dihydrazide (C6H14N4O2) is typically, used in the linking of glycoproteins, such as antibodies, in a site specific fashion following periodate oxidation.
Oxidation and coupling may conveniently be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.
Adipic dihydrazide (C6H14N4O2) can undergo acylation reaction, can cross-link with epoxy resin, and the chemical reaction of hydrazine and formaldehyde can change the smell and toxicity of formaldehyde.
Adipic dihydrazide (C6H14N4O2) is often used with diacetone acrylamide to make high-performance water-soluble coatings.

1. Adipic dihydrazide (C6H14N4O2) bifunctional compound, which can be cross-linked with sodium hyaluronate as a protein drug carrier.
Adipic dihydrazide (C6H14N4O2) plays a cross-linking role with diacetone acrylamide in the post-crosslinking of water emulsion and water-soluble polymer, such as water-based coatings, adhesives, fibers, plastic film treatment, hair spray, etc., and can also be used as epoxy powder coating curing agent And water-based coating additives, metal deactivators and other polymer additives and water treatment agents, indoor formaldehyde adsorbents and intermediate raw materials.

2. The same bifunctional crosslinking reagent is specially used for aldehydes to generate relatively stable hydrazone links.
In particular, Adipic dihydrazide (C6H14N4O2) is used to connect glycoproteins, such as antibodies.

3. The same type of bifunctional linker for aldehydes can produce relatively stable hydrazone linkage; for the linkage of carbohydrate proteins, such as antibodies, periodate oxidation reaction occurs at a specific form of position; at pH 5.0, oxidation reaction and coupling reaction can be carried out conveniently, hydrazide derived from low pKa value can avoid competitive reaction through primary amine

4, Adipic dihydrazide (C6H14N4O2) mainly used for epoxy powder coating curing agent and coating additives, metal deactivator and other polymer additives and water treatment agents.
ADIPOHYDRAZIDE
Adipohydrazide is a chemical used for cross-linking water-based emulsions.
Adipohydrazide can also be used as a hardener for certain epoxy resins.
Adipohydrazide is a symmetrical molecule with a C4 backbone, and the reactive group is C=ONHNH2.

CAS Number: 1071-93-8
EC Number: 213-999-5
Molecular Formula: C6H14N4O2
Molecular Weight: 174.20 g/mol

Synonyms: Hexanedihydrazide, Adipic dihydrazide, 1071-93-8, Adipic acid dihydrazide, Adipohydrazide, Hexanedihydrazide, Hexanedioic acid, dihydrazide, Adipyl hydrazide, Hexanediohydrazide, Adipic acid, dihydrazide, Adipoyldihydrazine, adipoyl dihydrazide, VK98I9YW5M, DTXSID0044361, Hexanedioic acid, 1,6-dihydrazide, NSC 3378, NSC-3378, EINECS 213-999-5, NSC 29542, NSC-29542, AI3-22640, WLN: ZMV4VMZ, EC 213-999-5, MFCD00007614, Adipodihydrazide, Adip dihydr, adipic hydrazide, Adipoyl hydrazide, adipic dihydrazone, Hexanedihydrazide #, Adipic aciddihydrazide, Adipic acid dihyrazide, Hexanedioic dihydrazide, AJICURE ADH, QUALIMER ADH, ULTRALINK HYDRAZIDE, Hexanedioic acid dihydrazide, SCHEMBL49856, Adipic Acid Dihydrazide (ADH), CHEMBL3185968, DTXCID8024361, SCHEMBL11037942, AMY3771, NSC3378, 1,4-Butanedicarboxylic dihydrazide, BK 1000Z, BT 1000Z, NSC29542, STR02658, Tox21_301067, BBL022965, STK709135, ADIPIC ACID DIHYDRAZIDE [INCI], AKOS000267183, NCGC00248276-01, NCGC00257525-01, CAS-1071-93-8, A0170, Adipic acid dihydrazide, >=98% (titration), CS-0010116, FT-0621914, EN300-03706, D72486, T 2210, Adipic acid dihydrazide, purum, >=97.0% (NT), A801603, J-660023, Q-200600, Q4682936, Z56812730, F1943-0024, Hexanedihydrazide, Adipic dihydrazide, Adipohydrazide, Adipyl hydrazide, Adipic acid dihydrazide, Adipyl hydrazide, Adipic acid dihyrazide, Hexanedioic acid, dihydrazide, 403, adipohydrazide, Hexanedioic Acid Dihydrazide, ADH, ADH (hydrazide), ADH 4S, ADH-J, ADH-S, Adipic dihydrazide, Adipoyl Dihydrazide, Adipoyl Hydrazide, Adipoyldihydrazine, Ajicure ADH, BK 1000Z, BT 1000Z, NSC 29542, NSC 3378, Qualimer ADH, T 2210, Adipohydrazide, Adipic dihydrazide, adipohydrazide, adipic acid dihydrazide, hexanedioic acid, dihydrazide, adipyl hydrazide, hexanediohydrazide, adipic acid, dihydrazide, adipodihydrazide, hexanedioic acid, 1,6-dihydrazide, unii-vk98i9yw5m, Hexanedioic acid,1,6-dihydrazide, Adipic acid dihydrazide, Hexanedioic acid,dihydrazide, Adipic dihydrazide, Adipoyl hydrazide, ADH, Adipoyl dihydrazide, Adipoyldihydrazine, Qualimer ADH, BT 1000Z, BK 1000Z, NSC 29542, NSC 3378, ADH 4S, ADH (hydrazide), ADH-J, ADH-S, T 2210, Ajicure ADH, Adipic acid dihydrazide, Technicure ADH, Epicure PD 797, 98152-55-7, 124246-54-4, ADH, Adipohydrazide, ADIPODIHYDRAZIDE, adipoyl hydrazide, Adipic dihydrazide, Adipic dihydrazide, ADIPINIC DIHYDRAZIDE, ADIPIC ACID DIHYDRIZIDE, ADIPIC ACID DIHYDRAZIDE

Adipohydrazide is a chemical used for cross-linking water-based emulsions.
Adipohydrazide is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.

Adipohydrazide is a latent hardener for epoxy resin.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).

Adipohydrazide is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Adipohydrazide is an effective crosslinking agent, curative and hardener.

Adipohydrazide is the most common dihydrazide crosslinking agent within a series of dihydrazides such as sebacic dihydrazide (SDH) and isophthalic dihydrazide (IDH).
Adipohydrazide’s has a melting point of 180 °C and a molecular weight of 174; both are lower than the alternative dihydrazides SDH and IDH.

Adipohydrazide is a symmetrical molecule with a C4 backbone and the reactive group is C=ONHNH2.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).

The applications of Adipohydrazide are facilitated by the nucleophilicity of the amine function (good reaction characteristics), the good overall properties and weatherability of cured systems.
The moderate solubility of Adipohydrazide in water (50 g./liter) and common organic solvents facilitates the use of Adipohydrazide in aqueous and solvent based systems.

The cure temperature for epoxy resins (glycidyl types) formulated with Adipohydrazide is influenced by the melt-out temperature of the Adipohydrazide, which allows an extended pot life at low temperatures.
Storage stability can be up to six-months at room temperature, with cure times of about one-hour at 130 °C.

Cure rates can be accelerated using tin or titanate catalysts, or imidazoles.
One-component Adipohydrazide epoxy systems can be partially cured or “B-staged”, and later fully cured.
B-staging provides handling, processing, and fabrication advantages.

Adipohydrazide is a distinctive crosslinking agent and curative that provides controlled reactivity and performance improvements in epoxy resins, polyurethane dispersions (PUDs), solvent-based polyurethanes (PURs), and emulsion acrylic resins.
Adipohydrazide finds major applications as a latent curing agent for B-stageable epoxy resins and as an ambient temperature crosslinking agent for high-performance acrylic emulsion architectural coatings.
Materials crosslinked or cured with Adipohydrazide demonstrate excellent colour stability, weathering resistance, adhesion, durability, hardness, and toughness.

Adipohydrazide is a chemical used for cross-linking water-based emulsions.
Adipohydrazide can also be used as a hardener for certain epoxy resins.

Adipohydrazide is a symmetrical molecule with a C4 backbone, and the reactive group is C=ONHNH2.
Dihydrazides are made by the reaction of an organic acid with hydrazine.
Other dihydrazides with different backbones are also common, including isophthalic dihydrazide (IDH) and sebacic dihydrazide (SDH).

Homobifunctional cross-linking reagent that is specific for aldehydes resulting in relatively stable hydrazone linkages.
This is commonly used in the linking of glycoproteins, such as antibodies, in a site specific fashion following periodate oxidation.

Adipohydrazide acts as a reducing agent in organic synthesis.
Adipohydrazide reduces aldehydes and ketones to alcohols, and Adipohydrazide reduces nitro compounds to amines.
Adipohydrazide also acts as a catalyst in the production of polyurethane foams, and Adipohydrazide is used as a cross-linking agent in polymers.

Adipohydrazide is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.
Adipohydrazide is also employed as a paint additive and coating additive.

Adipohydrazide is also used as an intermediate.
Further, Adipohydrazide is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.

Adipohydrazide is a homobifunctional cross-linking reagent that is specific for aldehydes.
This results in relatively stable hydrazone linkages.

Adipohydrazide is generally used in the linking of glycoproteins, like antibodies, in a site-specific fashion following periodate oxidation.
Oxidation and coupling may be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.

Adipohydrazide is the most suitable hydrazide cross-linking agent, and Adipohydrazide has been widely used in water-based paint emulsions in combination with diacetone acrylamide.
Adipohydrazide is weakly alkaline, and there is a possibility of agglomeration when solid Adipohydrazide is added directly to the emulsion, so usually Adipohydrazide should be dissolved in hot water before use.

Applications of Adipohydrazide:
Adipohydrazide is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.
Adipohydrazide is also employed as a paint additive and coating additive.

Adipohydrazide is also used as an intermediate.
Further, Adipohydrazide is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.

Adipohydrazide has been used:
Adipohydrazide is used in the preparation of reactive premix to synthesize the porous biomaterial.
Adipohydrazide is used for the crosslinking of methacrylated chondroitin sulfate (MA-CS) coating using carbodiimide-based chemistry for the production and characterization of methacrylated chondroitin sulfate magnetic nanoparticles (MA-CS MNPs).

Adipohydrazide is used for the covalent labeling of rhamnolipids, pyochelin, and vancomycin with Abberior STARNHS ester dye.
Adipohydrazide is used as a difunctional crosslinking agent in paints and coatings for certain water-based acrylic emulsions.

Adipohydrazide is used as a hardener for epoxy resins and a chain extender for polyurethanes.
A small use is as a formaldehyde scavenger preventing the liberation of formaldehyde.

Adipohydrazide is Applied in The Production of:
Crosslinking Agent for Polymers
Elastomers and Rubber Industry
Adhesives and Sealants
Coatings and Paints
Textile Industry
Corrosion Inhibitors
Biomedical Applications
Photography
Water Treatment
Fuel Additives
Polymer Modification

Uses of Adipohydrazide:
Adipohydrazide is used to functionalize magnetic nanoparticles for glycopeptide enrichment and identification.
Adipohydrazide is a homobifunctional cross-linking reagent specific for aldehydes resulting in relatively stable hydrazone linkages.

Adipohydrazide is typically, used in the linking of glycoproteins, such as antibodies, in a site specific fashion following periodate oxidation.
Oxidation and coupling may conveniently be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.

Adipohydrazide can also be used as a chain extension for liquid rubber.
Adipohydrazide can also be used as a hardener for certain epoxy resins.

Adipohydrazide is used adhesives and sealant chemicals, and Automotive care products.
Adipohydrazide is used for epoxy powder coating curing agent and coating additives, Metal deactivator and other polymer additives and water treatment agent.

Adipohydrazide is the most suitable hydrazide crosslinking agent.
Adipohydrazide and diacetone acrylamide have been widely used in water-based paint emulsion.
Adipohydrazide is weakly alkaline, solid Adipohydrazide is directly added to the emulsion may produce coalescence, usually Adipohydrazide should be dissolved in hot water (poor solubility in cold water) and reused.

Adipohydrazide bifunctional compound, which can be cross-linked with sodium hyaluronate as a protein drug carrier.
Adipohydrazide plays a cross-linking role with diacetone acrylamide in the post-crosslinking of water emulsion and water-soluble polymer, such as water-based coatings, adhesives, fibers, plastic film treatment, hair spray, etc., and can also be used as epoxy powder coating curing agent And water-based coating additives, metal deactivators and other polymer additives and water treatment agents, indoor formaldehyde adsorbents and intermediate raw materials.

The same type of bifunctional linker for aldehydes can produce relatively stable hydrazone linkage; for the linkage of carbohydrate proteins, such as antibodies, periodate oxidation reaction occurs at a specific form of position; at pH 5.0, oxidation reaction and coupling reaction can be carried out conveniently, hydrazide derived from low pKa value can avoid competitive reaction through primary amine.

Adipohydrazide is mainly used for epoxy powder coating curing agent and coating additives, metal deactivator and other polymer additives and water treatment agents.
Adipohydrazide is used as a crosslinking agent in acrylic emulsion with ketone group.

Adipohydrazide is used in epoxy adhesives and sealants.
Adipohydrazide is used crosslinking agent for self crosslinking emulsion resins using DAAM.
Adipohydrazide, also known as ADH or Adipic dihydrazide, can be used as a hardener for epoxy resins and for cross-linking water-based emulsions.

Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
Adipohydrazide is used analytical Reagents, Diagnostic Reagents, Teaching Reagents.

Adipohydrazide is used for Biological Purpose, For Tissue Medium Purpose, For Electron Microscopy, For Lens Blooming, Pro Analysis, Super Special Grade, For Scintillation, For Electrophoresis Use, For Refractive Index.
Adipohydrazide is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Adipohydrazide is used in the following products: coating products, adhesives and sealants, fillers, putties, plasters, modelling clay, finger paints, polymers, non-metal-surface treatment products, textile treatment products and dyes and washing & cleaning products.
The same bifunctional crosslinking reagent, Adipohydrazide, is specially used for aldehydes to generate relatively stable hydrazone links.

Other release to the environment of Adipohydrazide is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).
Other release to the environment of Adipohydrazide is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

Adipohydrazide can be found in complex articles, with no release intended: vehicles covered by End of Life Vehicles (ELV) directive (e.g. personal vehicles or delivery vans).
In particular, Adipohydrazide is used to connect glycoproteins, such as antibodies.

Adipohydrazide is used in the following products: adhesives and sealants, coating products, paper chemicals and dyes, textile treatment products and dyes and washing & cleaning products.
Adipohydrazide is used for the manufacture of: textile, leather or fur and wood and wood products.

Other release to the environment of Adipohydrazide is likely to occur from: outdoor use, indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

Adipohydrazide is used in the following products: adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, polymers, textile treatment products and dyes and finger paints.
Release to the environment of Adipohydrazide can occur from industrial use: formulation of mixtures and formulation in materials.

Adipohydrazide is used in the following products: paper chemicals and dyes, coating products, textile treatment products and dyes, adhesives and sealants, finger paints, laboratory chemicals, washing & cleaning products and water treatment chemicals.
Adipohydrazide is used for the manufacture of: chemicals, pulp, paper and paper products and plastic products.

Release to the environment of Adipohydrazide can occur from industrial use: for thermoplastic manufacture, as an intermediate step in further manufacturing of another substance (use of intermediates), in the production of articles and as processing aid.
Release to the environment of Adipohydrazide can occur from industrial use: manufacturing of the substance.

Adipohydrazide is a homobifunctional cross-linking reagent specific for aldehydes resulting in relatively stable hydrazone linkages.
Adipohydrazide is typically, used in the linking of glycoproteins, such as antibodies, in a site-specific fashion following periodate oxidation.
Oxidation and coupling may conveniently be performed at pH 5.0 due to the low pKa of the hydrazide which avoids competition by primary amines.

Adipohydrazide is used to functionalize magnetic nanoparticles for gylcopeptitde enrichment and identification.
Adipohydrazide can also be used as a chain extension for liquid rubber.

Adipohydrazide is used for synthesis.
Adipohydrazide is used as a formaldehyde scavenger and reacts with formaldehyde, thereby preventing the volatilizing of formaldehyde in the air.

Adipohydrazide is also employed as a paint additive and coating additive.
Adipohydrazide is also used as an intermediate.

Further, Adipohydrazide is used for cross-linking water-based emulsions and as a hardener for certain epoxy resins, which finds application in powder coating.
Adipohydrazide is widely used as cross-linker in waterborne acrylic emulsions.

Adipohydrazide is added to the water phase in a PUD.
Crosslinking occurs during the drying and film coalescence process which is ideal for maximizing the film properties including gloss, scrub, stain and wear resistance and durability.

Other crosslinking methods where crosslinking occurs prior to film coalescence exhibit reduced performance properties including poor flow and leveling.
The full reactivity characteristics of Adipohydrazide are ideal for PUR systems.
Alternative curatives which show incomplete crosslinking due to slow reactivity and the lack of curative mobility in a dry film will also compromise performance.

The DAAM/Adipohydrazide pair is also used in crosslinkable sizing agents, thickeners, adhesives, and sealants.
Adipohydrazide is a unique crosslinking agent and curative, offering controlled reactivity and performance enhancements in epoxy resins, polyurethane dispersions (PUDs), solvent based PURs and emulsion acrylic resins.

The major applications for Adipohydrazide are a latent curing agent for B-stageable epoxy resins and an ambient temperature crosslinking agent for high performance acrylic emulsion architectural coatings.
Systems crosslinked or cured with Adipohydrazide exhibit good color stability and weathering characteristics, adhesion, durability, hardness, and toughness.

Adipohydrazide is a chemical used for cross-linking water-based emulsions.
Adipohydrazide can also be used as a hardener for certain epoxy resins.

Adipohydrazide is used as a difunctional crosslinking agent in paints and coatings for certain water-based acrylic emulsions.
Adipohydrazide is used as a hardener for epoxy resins and a chain extender for polyurethanes.

A small use is as a formaldehyde scavenger preventing the liberation of formaldehyde.
One component epoxy resins are used in coatings such as powder coatings, adhesives including hot melt adhesives, molding compounds and in fiber reinforced composites.

Glass and carbon fiber prepreg obtained by a hot melt impregnation method are used in the fabrication of sporting goods, wind turbine blades and aircraft/aerospace components.
With Adipohydrazide cure, epoxy resins exhibit excellent toughness, flexibility, and adhesive properties.

Tg’s of 140-160 °C are achievable using a standard liquid bisphenol A epoxy resin (DGEBA) with Adipohydrazide as the hardener.
Rigid and flexible epoxy adhesives have been formulated as one component systems that can be stored at room temperature using Adipohydrazide as a latent curing agent.
Rigid epoxy adhesives are based on bisphenol A and novolac epoxides.

These rigid adhesives exhibit excellent cohesive and adhesive properties to a wide variety of surfaces.
Flexible epoxy adhesives produce more pliable bonds which better accommodate bond line stresses or differential substrate expansion rates.

Flexible epoxy resins include aliphatic di- and tri-epoxy resins such as hexanediol diglycidyl ether and poly(oxypropylene) diglycidyl ethers.
Semi-rigid epoxy-based adhesives utilize mixtures of both classes of epoxy resins or rigid formulations using flexibilizers.

Epoxy Resins:
A notable fact with regard to Adipohydrazide in epoxy formulations is that each of the primary amine end groups has a functionality of two, so the Adipohydrazide molecule has an equivalency of four per epoxy moiety.
Accordingly, the active hydrogen equivalent weight of Adipohydrazide is 43.5.
When formulated with epoxy resins, the Adipohydrazide index can range between 0.85-1.15 of stoichiometric proportions, without a significant effect on mechanical properties.

Industry Uses:
Adhesion/cohesion promoter
Binder
Hardener
Other (specify)
Paint additives and coating additives not described by other categories
Plasticizer

Consumer Uses:
Hardener
Other
Other (specify)
Paint additives and coating additives not described by other categories

Biochem/physiol Actions of Adipohydrazide:
Adipohydrazide is a low molecular weight compound that comprises a hydrazide group at each end.
This leads to the supply of extra adsorption sites for heavy metals that maintain or elevate the adsorption capacities of the cross-linked adsorbents.
Adipohydrazide is used as a crosslinker in various fields, like making mechanical latexes films and injectable oxidized hyaluronic acid hydrogel.

General Manufacturing Information of Adipohydrazide:

Industry Processing Sectors:
Adhesive Manufacturing
Custom Compounding of Purchased Resins
Paint and Coating Manufacturing
Paper Manufacturing
Plastics Product Manufacturing
Printing Ink Manufacturing

Typical Properties of Adipohydrazide:
Adipohydrazide is physical and chemical properties appearance white crystalline powder
Adipohydrazide is soluble in water, slightly soluble in acetone, and acetic anhydride or acid chloride can occur acylation reaction, is an important amide hydrazine compounds.

Adipohydrazide serves as a difunctional crosslinking agent in paints and coatings applied to specific water-based acrylic emulsions.
Additionally, Adipohydrazide acts as a hardener for epoxy resins and a chain extender for polyurethanes.
Moreover, Adipohydrazide finds a minor application as a formaldehyde scavenger, preventing the release of formaldehyde.

Polyurethane Dispersions (Puds):
Adipohydrazideis an effective room temperature curative for aqueous PUDs and solution polyurethanes.
In this capacity, Adipohydrazide provides polyurea coatings with higher hardness, toughness and adhesion properties, excellent mechanical properties, abrasion and chemical resistance.
Adipohydrazide cured polyurethane coatings exhibit good color stability and weathering properties, which is not observed with standard amine curatives.

Handling And Storage of Adipohydrazide:

Conditions for safe storage, including any incompatibilities:

Storage conditions:
Tightly closed.
Dry.

Storage stability:

Recommended storage temperature:
20 °C

Stability And Reactivity of Adipohydrazide:

Chemical stability:
Adipohydrazide is chemically stable under standard ambient conditions (room temperature).

First Aid Measures of Adipohydrazide:

If inhaled:

After inhalation:
Fresh air.

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.

In case of eye contact:

After eye contact:
Rinse out with plenty of water.
Remove contact lenses.

If swallowed:

After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.

Fire Fighting Measures of Adipohydrazide:

Extinguishing media:

Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder

Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.

Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

Accidental Release Measures of Adipohydrazide:

Environmental precautions:
Do not let product enter drains.

Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.

Observe possible material restrictions:
Take up dry.

Dispose of properly.
Clean up affected area.

Exposure Controls/personal Protection of Adipohydrazide:

Personal protective equipment:

Eye/face protection:
Use equipment for eye protection.
Safety glasses.

Skin protection:

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min

Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min

Control of environmental exposure:
Do not let product enter drains.

Identifiers of Adipohydrazide:
CAS number: 1071-93-8
EC number: 213-999-5
Hill Formula: C₆H₁₄N₄O₂
Molar Mass: 174.2 g/mol
HS Code: 2928 00 90
Flash point: 150 °C
Ignition temperature: 360 °C
Melting Point: 180 - 182 °C
Melting Point: 178.0°C to 182.0°C
Color: White to Yellow
Infrared Spectrum: Authentic
Assay Percent Range: 8%
Linear Formula: H2NNHCO(CH2)4CONHNH2
Beilstein: 02, I, 277
Solubility Information Solubility in water: soluble.
Other solubilities: soluble in acetic acid,slightly soluble in acetone,
insoluble in ethanol,ether and benzene
Formula Weight: 174.2
Percent Purity: 98%
Physical Form: Crystalline Powder

Molecular Weight: 174.20100
Exact Mass: 174.20
EC Number: 213-999-5
UNII: VK98I9YW5M
NSC Number: 29542|3378
DSSTox ID: DTXSID0044361
HScode: 2928000090
PSA: 110.24000
XLogP3: -2.1
Appearance: DryPowder
Density: 1.186 g/cm3
Melting Point: 171 °C @ Solvent: Water
Boiling Point: 519.3ºC at 760 mmHg
Flash Point: > 109ºC
Refractive Index: 1.513
Water Solubility: H2O: soluble
Storage Conditions: -20ºC
Vapor Pressure: 6.92E-11mmHg at 25°C

Properties of Adipohydrazide:
Molecular Weight: 174.20 g/mol
XLogP3-AA: -2.1
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 5
Exact Mass: 174.11167570 g/mol
Monoisotopic Mass: 174.11167570 g/mol
Topological Polar Surface Area: 110Ų
Heavy Atom Count: 12
Complexity: 142
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Physical state: powder
Color: white
Odor: No data available
Melting point/freezing point
Melting point/range: 180 - 182 °C - lit.
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 150 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 102 g/l at 20 °C - soluble
Partition coefficient:
n-octanol/water:
log Pow: -2,7 at 20 °C

Vapor pressure: No data available
Density: No data available
Relative density: 1,29 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available
Molecular Formula: C6H14N4O2
Molar Mass: 174.2
Density: 1.186g/cm3
Melting Point: 175-182℃
Boling Point: 519.3°C at 760 mmHg
Flash Point: 267.9°C
Water Solubility: soluble
Vapor Presure: 6.92E-11mmHg at 25°C
Appearance: White crystal

Storage Condition: 2-8℃
Sensitive: Sensitive to air
Refractive Index: 1.513
MDL: MFCD00007614
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 519.30 °C. @ 760.00 mm Hg (est)
Flash Point: 514.00 °F. TCC ( 267.90 °C. ) (est)
logP (o/w): -2.670 (est)
Soluble in: water, 3.287e+005 mg/L @ 25 °C (est)
Appearance (Colour): White to pale yellow
Appearance (Form): Powder
Solubility: (Turbidity) 10% aq. solution: Clear
Solubility: (Colour) 10% aq. solution: Colourless to pale yellow
Assay (NT): min. 95.0%
Melting Point: 178 - 182°C
Loss on drying: max. 0.5%

CAS Number: 1071-93-8
Abbreviations: ADH
Beilstein Reference: 973863
ChemSpider: 59505
ECHA InfoCard: 100.012.727
EC Number: 213-999-5
MeSH: Adipic+dihydrazide
PubChem CID: 66117
RTECS number: AV1400000
UNII: VK98I9YW5M
CompTox Dashboard (EPA): DTXSID0044361
InChI: InChI=1S/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12)
Key: IBVAQQYNSHJXBV-UHFFFAOYSA-N
InChI=1/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12)
Key: IBVAQQYNSHJXBV-UHFFFAOYAB
SMILES: O=C(NN)CCCCC(=O)NN

Specifications of Adipohydrazide:
Color according to Munsell color system: not more intensely colored than reference standard NE12
Assay (HClO₄): ≥ 97.0 %
Melting range (lower value): ≥ 178 °C
Melting range (upper value): ≤ 182 °C
Identity (IR): passes test

Melting Point: 180 - 183 Deg C:
Fe: <0.0005%:
Loss on Drying: <0.5%:
Sulfate: <0.005%:
Assay: >99%:
Methanol: <0.1%:
Non Volatile Matter: <0.01%:
Cl: <0.005%:
Appearance: White crystalline powder:
Hydrazine: <20ppm

Related compounds of Adipohydrazide:
hexanedioic acid
hexanedihydrazide
hexanedioyl dichloride
hexanedinitrile
hexanediamide

Names of Adipohydrazide:

Preferred IUPAC name:
Hexanedihydrazide

Other names:
Adipohydrazide
Adipic dihydrazide
Adipyl hydrazide
ADUXOL STA 05 D
Silicon dioxide; AEROSIL(TM) 200; BAKER SILICA GEL; CAB-OSIL M-5; CAB-O-SIL(TM) M-5; COLLOIDAL SILICA; CRISTOBALITE; DAVISIL(TM); DRYING PEARLS ORANGE; IATROBEADS; LICHROSORB(R) 60; PHTHALOCYANINE IMMOBILIZED SILICA GEL; POTASSIUM HYDROXIDE-IMPREGNATED SILICA GEL; PRESEP(R) SILICA GEL TYPE 3L; QUARTZ; SAND; SILICA; SILICA GEL; SILICA GEL 100; SILICA GEL 12-28 MESH; SILICA GEL 30 CAS NO:112945-52-5