Water Treatment, Metal and Mining Chemicals

3-IODO-2-PROPYNYL BUTYLCARBAMATE (IPBC)
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate ester
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is carbamic acid in which the nitrogen has been substituted by a butyl group and in which the hydrogen of the carboxy group is replaced by a 1-iodoprop-2-yn-3-yl group.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a fungicide


CAS NUMBER: 55406-53-6

EC NUMBER: 259-627-5

MOLECULAR FORMULA: C8H12INO2

MOLECULAR WEIGHT: 281.09 g/mol

IUPAC NAME: 3-iodoprop-2-ynyl N-butylcarbamate


3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a preservative and sapstain control chemical in wood products
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a preservative in adhesives, paints, latex paper coating, plastic, water-based inks, metal working fluids, textiles, and numerous consumer products.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) has a role as a xenobiotic, an environmental contaminant
3-Iodo-2-Propynyl Butylcarbamate (IPBC) also has a role as an antifungal agrochemical.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate ester
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is an organoiodine compound

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is an acetylenic compound and a carbamate fungicide.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate pesticide.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is derived from carbamic acid
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is widely used in homes, gardens and agriculture.

Some of the carbamates are translocated within plants, making them an effective systemic treatment.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a water-soluble preservative

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used globally in the paints & coatings
3-Iodo-2-Propynyl Butylcarbamate (IPBC) can be used in wood preservatives

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is also used in personal care, and cosmetics industries.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a member of the carbamate family of biocides.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) was invented in the 1970s
3-Iodo-2-Propynyl Butylcarbamate (IPBC) has a long history of effective use as an antifungal technology.

History:
3-Iodo-2-Propynyl Butylcarbamate (IPBC) was initially developed for use in the paint & coatings industry as a dry-film preservative to protect interior and exterior coatings from mold, mildew, and fungal growth, while also offering cost performance and sustainability benefits.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) exhibits efficacy against a broad spectrum of fungal species, typically at very low use levels.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) today is incorporated into a wide variety of interior and exterior paint formulations around the world.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used in the following products:
-cosmetics
-personal care products
-perfumes
-fragrances
-laboratory chemicals

3-Iodo-2-Propynyl Butylcarbamate (IPBC) belongs to the class of organic compounds known as carboximidic acids and derivatives.
Carboximidic acids and derivatives are compounds containing a carboximidic group, with the general formula R-C(=NR1)OR2.

Alternative Classes:
*Propargyl-type 1,3-dipolar organic compounds
*Haloacetylenes and derivatives
*Organopnictogen compounds
*Organooxygen compounds
*Organonitrogen compounds
*Organoiodides
*Hydrocarbon derivatives

Substituents :
*Haloacetylene or derivatives
*Organic 1,3-dipolar compound
*Propargyl-type 1,3-dipolar organic compound
*Carboximidic acid derivative
*Organic nitrogen compound
*Organic oxygen compound
*Organopnictogen compound
*Hydrocarbon derivative
*Organooxygen compound
*Organonitrogen compound
*Organoiodide
*Organohalogen compound
*Aliphatic acyclic compound

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is also referred to as iodopropynyl butylcarbamate (IPBC).
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is widely used as antifungal[1] and anti-microbial agent
3-Iodo-2-Propynyl Butylcarbamate (IPBC) can be encapsulated in polystrene/polycaprolactone blend in the form microspheres.


PHYSICAL PROPERTIES:

-Molecular Weight: 281.09 g/mol

-XLogP3-AA: 2.1

-Exact Mass: 280.99128 g/mol

-Monoisotopic Mass: 280.99128 g/mol

-Topological Polar Surface Area: 38.3Ų

-Physical Description: White solid with a pungent odor

-Color: Off-white

-Form: Solid

-Odor: Sharp pungent odor

-Melting Point: 66 °C

-Solubility: 156 mg/L

-Density: 1.575 g/mL

-Vapor Pressure: 0.0000525 mmHg


3-Iodo-2-Propynyl Butylcarbamate (IPBC) is an additive in a white, crystalline powder form.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a broad based biocide used globally as a preservative, fungicide, and algaecide.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is most commonly used as a preservative in paint and coating applications.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is an off-white solid


CHEMICAL PROPERTIES:

-Hydrogen Bond Donor Count: 1

-Hydrogen Bond Acceptor Count: 2

-Rotatable Bond Count: 5

-Heavy Atom Count: 12

-Formal Charge: 0

-Complexity: 192

-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 Classes: Other Uses -> Biocides/Disinfectants


3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate ester that is carbamic acid in which the nitrogen has been substituted by a butyl group and in which the hydrogen of the carboxy group is replaced by a 1-iodoprop-2-yn-3-yl group.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a preservative and sapstain control chemical in wood product

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a preservative in:
-adhesives
-paints
-latex paper coating
-plastic
-water-based inks
-metal working fluids
-textiles
-numerous consumer products

3-Iodo-2-Propynyl Butylcarbamate (IPBC) has a role as a xenobiotic, an environmental contaminant and an antifungal agrochemical.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate ester, an organoiodine compound

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is an acetylenic compound
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a carbamate fungicide.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a biocide and preservative in paints, cosmetics, and other products
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used as a preservative in personal care formulations


APPLICATIONS:

-Cosmetics
-Wood preservatives
-Paints
-Metalworking fluids
-Household products
-Moistened toilet tissues
-Contact lenses
-Building materials
-Cooling water
-Adhesives
-Textiles
-Paper


3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a preservative with broad fungicidal activity
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is used in skin care products.

3-Iodo-2-Propynyl Butylcarbamate (IPBC) is recommended for use in difficult formulation systems.
3-Iodo-2-Propynyl Butylcarbamate (IPBC) is a highly effective fungicide as well as a bactericide.


SYNONYMS:

55406-53-6
3-iodoprop-2-yn-1-yl butylcarbamate
Iodopropynyl butylcarbamate
3-Iodo-2-propynyl butylcarbamate
Iodocarb
Ipbc
3-Iodo-2-propynyl N-butylcarbamate
1-Iodoprop-1-yn-3-yl N-n-butylcarbamate
3-iodoprop-2-ynyl N-butylcarbamate
Carbamic acid, butyl-, 3-iodo-2-propynyl ester
Troysan KK-108A
3-IODO-2-PROPYNYLBUTYLCARBAMATE
3-Iodo-2-propynyl-N-butylcarbamate
Butyl-3-iodo-2-propynylcarbamate
3-iodoprop-2-yn-1-yl N-butylcarbamate
603P14DHEB
DTXSID0028038
CHEBI:83279
3-iodoprop-2-ynyl butylcarbamate
3-Iodo-2-propynyl N-Butylcarbamate-d9
DTXCID908038
1246815-08-6
Caswell No. 501A
CAS-55406-53-6
HSDB 7314
3-Iodo-2-propynyl butyl carbamate
EINECS 259-627-5
EPA Pesticide Chemical Code 107801
BRN 2248232
iodocarbe
UNII-603P14DHEB
C8H12INO2
3-iodo-2-propynyl-N-butyl carbamate
3-iodo-2-propyn-1-yl N-butylcarbamate
Carbamic acid, butyl-3-iodo-2-propynyl ester
IPBC
iodo-2-propynylbutylcarbamate
SCHEMBL114369
CHEMBL1893913
3-Iodo-2-propynyl butylcarbamate #
3-iodoprop-2-yn-1-ylbutylcarbamate
MFCD00072438
AKOS015905567
CS-W010051
GS-3240
Iodocarb 100 microg/mL in Acetonitrile
NCGC00164376-01
NCGC00164376-02
NCGC00164376-03
NCGC00164376-04
NCGC00164376-05
NCGC00255017-01
NCGC00259413-01
IODOPROPYNYL BUTYLCARBAMATE [INCI]
3-Iodo-2-propynyl N-butylcarbamate, 97%
3-Iodo-2-propynyl N-Butylcarbamate-[d9]
IODOPROPYNYL BUTYLCARBAMATE [VANDF]
3-IODO-2-PROPYNYL BUTYL CARBBAMATE
FT-0615885
I0666
IODOPROPYNYL BUTYL CARBAMATE [MART.]
N-Butylcarbamic Acid 3-Iodo-2-propynyl Ester
3-IODO-2-PROPYNYLBUTYLCARBAMATE [HSDB]
A830629
Q2928998
W-105563
Carbamic acid, N-butyl-, 3-iodo-2-propyn-1-yl ester
3-Iodo-2-propynyl N-butylcarbamate, analytical standard
3-iodo-2-propynyl butyl Carbamate
3-iodo-2-propynyl butylcarbamate
3-iodo-2-propynyl butylcarbamate
3-iodo-2-propynyl butylcarbamate 3-iodoprop-2-yn-1-yl butylcarbamate
3-iodo-2-propynyl butylcarbamate; 3-iodoprop-2-yn-1-yl butylcarbamate
3-iodoprop-2-yn-1-yl butylcarbamate
Butyl-3-iodo-2-propynylcarbamate
Carbamic acid, butyl-3-iodo-2-propynyl ester
Carbamic acid, N-butyl-, 3-iodo-2-propyn-1-yl ester
Iodopropynyl butylcarbamate
3-Iodo-2-propinylbutyl carbamate
3-Iodo-2-propynyl butyl carbamate
3-iodo-2-propynyl butyl carbamate
3-IODO-2-PROPYNYL BUTYLCARBAMATE
3-Iodo-2-propynyl butylcarbamate
3-iodo-2-propynyl butylcarbamate
3-iodo-2-propynyl butylcarbamate (part of prep.)
3-iodo-2-propynyl butylcarbamate; 3-iodoprop-2-yn-1-yl butylcarbamate
3-Iodo-2-propynyl N-Butylcarbamate
3-Iodo-2-propynyl N-butylcarbamate
3-IODO-2-PROPYNYL-N-BUTYLCARBAMATE
3-iodoprop-2-yn-1-yl butylcarbamate
3-iodoprop-2-yn-1-yl N-butylcarbamate
3-iodoprop-2-ynyl N butylcarbamate
3-iodoprop-2-ynyl N-butylcarbamate
Carbamic acid, N-butyl-, 3-iodo-2-propyn-1-yl ester
Iodopropynylbutylcarbamate (IPBC)
IPBC, Omacide IPBC
3-Iodo-2-propynyl butyl carbamic acid
3-Iodo-2-propynyl butylcarbamate
3-Iodo-2-propynyl N-butylcarbamate
3-iodo-2-propynyl-butylcarbamate
3-iodo-2-propynylbutylcarbamate
3-iodoprop-2-yn-1-yl butylcarbamate
3-IPBC
Butyl-3-iodo-2-propynylcarbamate
Carbamic acid, butyl-, 3-iodo-2-propynyl ester
Carbamic acid, butyl-3-iodo-2-propynyl ester
IPBC
3-IODO-2-PROPYNYL BUTYLCARBAMATE
3-IODO-2-PROPYNYL N-BUTYLCARBAMATE
IBP
lodopropynyl butylcarbamate
IODOCARB
troysanpolyphaseanti-mildew
woodlife;
PERMATOX
Glycacil

3-MERCAPTOPROPIONIC ACID (3-MPA)
3-Mercaptopropionic acid (3-MPA) is used as a self-assembled monolayer (SAM) with a thiol and carboxylic groups.
3-Mercaptopropionic acid (3-MPA) has short carbon chains and is mainly used as a capping agent on a variety of nanoparticles.
3-Mercaptopropionic acid (3-MPA) that is propanoic acid carrying a sulfanyl group at position 3.

CAS: 107-96-0
MF: C3H6O2S
MW: 106.14
EINECS: 203-537-0

3-Mercaptopropionic acid (3-MPA) is an organosulfur compound with the formula HSCH2CH2CO2H.
3-Mercaptopropionic acid (3-MPA) is a bifunctional molecule, containing both carboxylic acid and thiol groups.
3-Mercaptopropionic acid (3-MPA) is a colorless oil.
3-Mercaptopropionic acid (3-MPA) is derived from the addition of hydrogen sulfide to acrylic acid.
3-Mercaptopropionic acid (3-MPA) is a mercaptopropanoic acid that is propanoic acid carrying a sulfanyl group at position 3.
3-Mercaptopropionic acid (3-MPA) has a role as an algal metabolite.
3-Mercaptopropionic acid (3-MPA) is a conjugate acid of a 3-mercaptopropionate.

3-Mercaptopropionic acid (3-MPA) Chemical Properties
Melting point: 15-18 °C (lit.)
Boiling point: 110-111 °C/15 mmHg (lit.)
Density: 1.218 g/mL at 25 °C (lit.)
Vapor pressure: 0.04 mm Hg ( 20 °C)
Refractive index: n20/D 1.492(lit.)
FEMA: 4587 | 3-MERCAPTOPROPIONIC ACID
Fp: 201 °F
Storage temp.: Store below +30°C.
Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka: pK1:;pK2:10.84(SH) (25°C)
Form: Crystalline Powder, Crystals, and/or Chunks
Color: White
Specific Gravity: 1.218
PH: 2 (120g/l, H2O, 20℃)
Odor: sulfurous roasted
Odor Type: sulfurous
Explosive limit: 1.60%(V)
Water Solubility: soluble
Sensitive: Air Sensitive & Hygroscopic
JECFA Number: 1936
BRN: 773807
Stability: Air Sensitive, Hygroscopic
InChIKey: DKIDEFUBRARXTE-UHFFFAOYSA-N
LogP: -2.3 at 22℃
CAS DataBase Reference: 107-96-0(CAS DataBase Reference)
NIST Chemistry Reference: 3-Mercaptopropionic acid (3-MPA) (107-96-0)
EPA Substance Registry System: 3-Mercaptopropionic acid (3-MPA) (107-96-0)

Uses
A compound suitable for amino acid analysis by means of OPA.
3-Mercaptopropionic acid (3-MPA) is widely used in food and beverage industries as a flavoring agent.
3-Mercaptopropionic acid (3-MPA) is used in the production of PVC stabilizers, which are used as chain transfer agents in polymerizations.
3-Mercaptopropionic acid (3-MPA) can be used as primary or secondary, color stabilizer in combination with phenolic antioxidant for polymers.
3-Mercaptopropionic acid (3-MPA) acts as a sulfide ion equivalent and is utilized in the preparation of diaryl sulfide from aryl iodide.

Reactions
3-Mercaptopropionic acid (3-MPA) is competitive inhibitor of glutamate decarboxylase, and therefore acts as a convulsant.
3-Mercaptopropionic acid (3-MPA) has higher potency and faster onset of action compared to allylglycine.
3-Mercaptopropionic acid (3-MPA) is used to prepare hydrophilic gold nanoparticles, exploiting the affinity of gold for sulfur ligands.

Synonyms
3-MERCAPTOPROPIONIC ACID
107-96-0
3-Mercaptopropanoic acid
3-Sulfanylpropanoic acid
3-Thiopropionic acid
3-Thiopropanoic acid
beta-Mercaptopropionic acid
Mercaptopropionic acid
Propanoic acid, 3-mercapto-
3MPA
2-Mercaptoethanecarboxylic acid
beta-Thiopropionic acid
Hydracrylic acid, 3-thio-
Propionic acid, 3-mercapto-
Thiohydracrylic acid
beta-Mercaptopropanoic acid
NSC 437
.beta.-Thiopropionic acid
UNII-B03TJ3QU9M
.beta.-Mercaptopropionic acid
C3H6O2S
Propionic acid, 3-mercpato-
3-Thiolpropanoic acid
3-thiohydracrylic acid
3-Mercaptopropionicacid
HSDB 5381
EINECS 203-537-0
3-mercapto-propionic acid
Mercaptopropionic acid, 3-
BRN 0773807
B03TJ3QU9M
.beta.-Mercaptopropanoic acid
AI3-26090
CHEMBL358697
DTXSID8026775
CHEBI:44111
NSC-437
EC 203-537-0
4-03-00-00726 (Beilstein Handbook Reference)
beta-Mercaptopropionate
3 Mercaptopropionic Acid
MFCD00004897
3-mercaptopropionsyre
BMPA
DEAMINO CYSTEINE
ss--Thiopropionic acid
betamercaptopropionic acid
3- mercaptopropionic acid
3-mercapto-propanoic acid
Propionic acid, mercapto-
ss--Mercaptopropanoic acid
ss--Mercaptopropionic acid
3-Sulfanylpropanoic acid #
SCHEMBL7289
USAF E-5
3-Mercaptopropanoic acid, 9CI
DTXCID106775
NSC437
3-Mercaptopropionic acid, 98%
FEMA NO. 4587
3-Mercaptopropionic acid, >=99%
AMY27767
BCP16636
STR01222
Tox21_200194
BDBM50121953
MERCAPTOPROPIONIC ACID [INCI]
STL281859
Thiopropionic acid; 3-Thiopropanoic acid; beta-Mercaptopropionic acid
AKOS000121541
AC-4722
AT21041
SB66313
3-MERCAPTOPROPIONIC ACID [HSDB]
propionic acid, 3-mercapto-methyl ester
NCGC00248556-01
NCGC00257748-01
BP-21405
CAS-107-96-0
LS-124729
LS-124730
FT-0615955
FT-0658630
M0061
3-Mercaptopropionic acid, >=99.0% (HPLC)
EN300-19579
3-Dimethylamino-2-methylpropylchloridehydrochloride
A801785
J-512742
Q11751618
F2191-0215
Z104474322
InChI=1/C3H6O2S/c4-3(5)1-2-6/h6H,1-2H2,(H,4,5
68307-97-1
3-METHOXYBUTANOL
3-METHOXYBUTANOL = 3-METHOXY-1-BUTANOL


CAS Number: 2517-43-3
EC Number: 219-741-8
MDL number: MFCD00002931
Molecular Formula: C5H12O2 / CH3CH(OCH3)CH2CH2OH


3-methoxybutanol is colorless liquid compound, which is difficult to ignite and has no odor.
3-methoxybutanol is water soluble and its boiling point is 161°C.
3-methoxybutanol is colorless transparent liquid.
3-methoxybutanol's Melting Point is -85 °c, boiling point 158-159 °c, relative density 0.971(20/20 °c), refractive index 1.4151, Flash Point 46 °C.


3-methoxybutanol is soluble in most organic solvents, insoluble in water.
The analysts forecast the global 3-methoxybutanol market to exhibit a CAGR of 5.01% during the period 2019-2024.
3-methoxybutanol is a glycol ether that is soluble in water. It has the chemical formula C4H10O2 and is a colorless liquid with a low viscosity.
3-Methoxy-1-butanol has been shown to react with glycols and alcohols to produce polymers with good film forming properties.


3-methoxybutanol also has active substances such as hydroxy group, nitrogen atoms, and particle.
3-methoxybutanol is a primary alcohol that is butane-1,3-diol in which the hydroxy group at position 3 is replaced by a methoxy group.
3-methoxybutanol is a primary alcohol and an ether.
3-methoxybutanol is functionally related to a butane-1,3-diol.


3-methoxybutanol acts as a low volatility, colorless, neutral solvent.
3-methoxybutanol possesses a mild odor and good dis-solving power for many natural resins, nitrocellulose, benzyl cellulose, polyvinyl butyrals, alde-hyde, ketone and indene resins, phenol-formaldehyde, urea-form-aldehyde and melamine-formalde-hyde resins, carbamic acid ester resin, alkyd and maleic resins.


3-methoxy butanol is a colourless liquid with a mild odour.
3-Methoxy Butanol is a colorless, neutral liquid with a mild odor.
3-methoxybutanol is miscible with water and the commonly used organic solvents.
3-methoxybutanol is Colorless transparent liquid.


3-methoxybutanol is the vapor forms an explosive mixture with air.
3-methoxybutanol reacts easily with oxidizing agents.
3-methoxybutanol is soluble in most organic solvents, slightly soluble in water.



USES and APPLICATIONS of 3-METHOXYBUTANOL:
3-methoxybutanol (CAS# 2517-43-3) is used as a reactant in the preparation of 3-​(1,​1-​dioxo-​2H-​(1,​2,​4)​-​benzothiadiazin-​3-​yl)​-​4-​hydroxy-​2(1H)​-​quinolinones as potent inhibitors of Hepatitis C Virus RNA-Dependent RNA Polymerase.
3-methoxybutanol is used as a high boiling point solvent, nitro cellulose paint, epoxy resin coating, brake oil viscosity regulator, printing ink solvent, cutting oil, dyes, pigments, pesticides, vinyl chloride safety agents and other solvents.


3-methoxybutanol is also used as an intermediate for home medicine and medicine, and the acetate prepared from it is also an excellent high boiling point solvent.
3-methoxybutanol is used as a solvent or cosolvent in coatings, inks and adhesives.
For instance, 3-methoxybutanol is used in nitrocellulose brush lacquers to improve brushability and flow, and in alkyd paints to improve brushability.


3-methoxybutanol is used in conjunction with Butoxyl to achieve special effects through dissolving power, drying time and flow.
3-methoxybutanol is used as a solvent or co-solvent in coatings, inks and adhesives.
For instance, it is used in nitrocellulose brush lacquers to improve brush ability and flow, and in alkyd paints to improve brush ability.
3-methoxybutanol is used in conjunction with Butoxyl to achieve special effects through dissolving power, drying time and flow.


3-methoxybutanol can function as rheology modifier or as a levelling agent in the paint & coatings system.
3-methoxybutanol also retards skinning.
3-methoxybutanol also appears under: Adhesives and Lubricants, Electronics, Packaging and Printing inks
3-methoxybutanol is a colourless liquid with a mild odour.


3-methoxybutanol is used in various applications because of its good dissolving power, drying time and flow.
Being a low-volatile solvent, 3-methoxybutanol is used in spray paints, adhesives, coatings and inks.
3-methoxybutanol is also used in lacquers to improve brushability and flow.
3-methoxybutanol is used as an intermediate to make 3-methoxy butyl acetate which is used as a cleaning solvent in the electronic industry.


Cosmetic Uses of 3-methoxybutanol: solvents
3-methoxybutanol improves brushability and flow.
3-methoxybutanol retards skinning in conventional and aqueous paints.
3-methoxybutanol shows miscibility with water and commonly used organic solvents.


3-methoxybutanol is used in nitrocellulose brush lacquers.
3-methoxybutanol is used high-boiling lacquer solvent, coupling agent for brake fluids, intermediate for plasticizers, herbicides, film-forming additive in PVA emulsions, solvent for pharmaceuticals.
3-methoxybutanol is used in various applications because of its good dissolving power, drying time and flow.


Besides good dissolving power, 3-methoxybutanol – as a low-volatility solvent – has similar advantages to n-Butanol.
3-methoxybutanol is used in nitrocellulose brush lacquers to improve brush ability and flow.
Small additions considerably reduce the viscosity of alkyd resin and oleo resinous paints and improve their brushability.
In conventional and aqueous paints, the addition of 3-methoxybutanol retards skinning.
3-methoxybutanol can be used with n-Butyl Acetate to achieve special effects in relation to dissolving power, drying time and flow.


3-methoxybutanol can also be used in combination with Butoxyl (3-Methoxy-n-Butylacetate).
3-methoxybutanol as a high boiling point solvent, is used in nitrocellulose paint, epoxy resin coating, brake oil viscosity regulator, printing ink solvent, cutting oil and dyes, pigments, pesticides, vinyl chloride stabilizer and other solvents.
3-methoxybutanol is also used as intermediates of medicine and medicine, and the acetate obtained from it is also an excellent solvent with high boiling point.


3-methoxybutanol is used as a high boiling point solvent for nitrocellulose paints, epoxy resin paints, brake oil viscosity modifiers, printing ink solvents, cutting oils and dyes, pigments, pesticides, vinyl chloride stabilizers and other solvents.
3-methoxybutanol is also used as an intermediate of home medicine and medicine, and the acetate obtained from it is also an excellent high boiling point solvent.


-3-methoxybutanol can be used as:
*A solvent in the synthesis of potassium 3-methoxy-1-butylxanthate, an intermediate used in the preparation of xanthate complexes.
*A model compound in the study of dehydration of alcohols using CeO2 as a catalyst.
*An intermediate to synthesize perylene diimide-based dyes applicable as the colorant of the black matrix.



PRODUCTION METHOD OF 3-METHOXYBUTANOL:
3-methoxybutanol is obtained by reacting butenal and methanol under alkali catalysis to generate methoxybutyraldehyde, which is then hydrogenated.
In the addition reaction of butenal and methanol, even if excessive methanol is used, the conversion rate is only 95% when reaching equilibrium, and 5% of unreacted butenal needs to be recovered.
The reaction is generally carried out at about 0 ℃ for 2 hours.
The generated methoxybutyraldehyde is a 50% methanol solution, neutralized with acetic acid, and then hydrogenated with nickel catalyst at 100-130 ℃ and about 25MPa.
Methoxybutyraldehyde is very unstable, so be careful when hydrogenating.



PRODUCTION METHOD AND OTHERS OF 3-METHOXYBUTANOL:
3-methoxybutanol is obtained by reacting crotonaldehyde and methanol under alkali catalysis to generate methoxybutyraldehyde, and then hydrogenating it.
For the addition reaction of crotonaldehyde and methanol , even if excess methanol is used, the conversion rate is only 95% when reaching equilibrium, and 5% of unreacted crotonaldehyde needs to be recovered.
The reaction is generally carried out at about 0°C for 2h.
The resulting methanol solution of 50% methoxybutyraldehyde is neutralized with acetic acid , and hydrogenation is carried out at 100-130°C under a pressure of about 25MPa using a nickel catalyst. Methoxybutyraldehyde is very unstable, so be careful when adding hydrogen.



DISSOLVING POWER:
3-Methoxy Butanol has good dissolving power for many natural resins, nitrocellulose, benzyl cellulose, polyvinyl butyrals, aldehyde, ketone and indene resins, phenol-formaldehyde, ureaformaldehyde and melamine-formaldehyde resins, carbamic acid ester resin, alkyd and maleic resins, the commonly used plasticizers and most fats and drying oils such as linseed oil, castor oil
and wood oil.



3-METHOXYBUTANOL DOES NOT DISSOLVE:
petroleum oils, waxes, rubber, chlorinated rubber, acetyl cellulose, polyisobutylene, polystyrene, non-post-chlorinated polyvinyl chloride (coatings), vinyl acetate/vinyl chloride/dicarboxylic acid copolymer, polyvinyl formal, polyvinyl carbazole and coumarone resin.
Ethyl cellulose, cellulose acetobutyrate, polyvinyl acetates and polyvinyl isobutyl ether swell considerably in 3-Methoxy Butanol.



PHYSICAL and CHEMICAL PROPERTIES of 3-METHOXYBUTANOL:
Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 0.92100 to 0.92400 @ 20.00 °C.
Pounds per Gallon - (est).: 7.673 to 7.698
Refractive Index: 1.41500 to 1.41700 @ 20.00 °C.
Melting Point: -85.00 °C. @ 760.00 mm Hg
Boiling Point: 159.00 to 163.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.738000 mmHg @ 25.00 °C. (est)
Flash Point: 117.00 °F. TCC ( 47.00 °C. )
logP (o/w): 0.070 (est)
Soluble in: alcohol, water, 3.662e+005 mg/L @ 25 °C (est)
Molecular Weight: 104.15
XLogP3-AA: 0.2
Hydrogen Bond Donor Count: 1

Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 3
Exact Mass: 104.083729621
Monoisotopic Mass: 104.083729621
Topological Polar Surface Area: 29.5 Ų
Heavy Atom Count: 7
Formal Charge: 0
Complexity: 37.1
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

Appearance Form: liquid
Colour: colourless
Odour: mild
Odour Threshold: No data available
pH: No data available
Melting point/freezing point: -85 °C at 1.013 hPa
Initial boiling point and boiling range: 157 °C at 1.013 hPa
Flash point: 67 °C - closed cup
Evaporation rate: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Vapour pressure: 0,17 hPa at 20 °C
Vapour density: No data available
Relative density: 0,928 g/cm3 at 25 °C
Water solubility: No data available

Partition coefficient:
n-octanol/water: No data available
Auto-ignition temperature: No data available
Decomposition temperature: No data available
Viscosity: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available
Density: 0.9200g/mL
Color: Colorless
Melting Point: -85.0°C
Boiling Point: 161.0°C
Flash Point: 46°C
Assay Percent Range: 98.5% min. (GC)
Infrared Spectrum: Authentic
Linear Formula: CH3CH(OCH3)CH2CH2OH

Density: 0.928
Melting point: -85 ºC
Boiling point: 161 ºC
Refractive index: 1.415-1.4165
Flash point: 46 ºC
Water solubility: SOLUBLE
Molecular Formula: C5H12O2
Molar Mass: 104.15
Density: 0.928g/mLat 25°C(lit.)
Melting Point: -85 °C
Boling Point: 161 °C
Flash Point: 116°F
Water Solubility: SOLUBLE
Vapor Presure: 17-460Pa at 20-50℃
Appearance: Liquid

Color: Clear colorless
pKa: 14.90±0.10(Predicted)
Refractive Index: n20/D 1.416(lit.)
Melting point: -85 °C
Boiling point: 161 °C
Density: 0.928 g/mL at 25 °C(lit.)
vapor pressure: 17-460Pa at 20-50℃
refractive index: n20/D 1.416(lit.)
Flash point: 116 °F
form: Liquid
pka: 14.90±0.10(Predicted)
color: Clear colorless
LogP: 0.002 at 25℃ and pH7

Molar mass g/mol: 104.15
Boiling point at 1013 hPa °C: 157
Melting temperature °C: – 85
Density at 20 °C g/cm3: 0.923
Refractive index nD at 20 °C (DIN 51 423, part 2): 1.415 – 1.416
Evaporation number (DIN 53 249, diethylether = 1): 160
Specific heat at 20 °C kJ/kg · K: 0.53
Heat of Vaporization at 1013 hPa J/kg: 116
Water absorption at 20 °C % (w/w): ∞
Solubility in water at 20 °C % (w/w): ∞
Vapour pressure at 20 °C hPa: 0.17
at 50 °C hPa: 4.6
Viscosity at 20 °C mPa · s: 3.7
Dielectric constant at 20 °C (DIN 53 483): 14.4
Electrical Conductivity at 20 °C S · cm-1 : 1.2 · 10–6



FIRST AID MEASURES of 3-METHOXYBUTANOL:
-Description of first aid measures:
*General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact
Flush eyes with water as a precaution.
*If swallowed:
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of 3-METHOXYBUTANOL:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Contain spillage, and then collect with non-combustible absorbent material, (e.g. sand, earth, diatomaceous earth, vermiculite) and place in container for disposal according to local / national regulations.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of 3-METHOXYBUTANOL:
-Extinguishing media
*Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
*Unsuitable extinguishing media
Do NOT use water jet.
-Advice for firefighters
Wear self-contained breathing apparatus for firefighting if necessary.
-Further information
Use water spray to cool unopened containers.



EXPOSURE CONTROLS/PERSONAL PROTECTION of 3-METHOXYBUTANOL:
-Control parameters:
--Components with workplace control parameters:
-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:
Safety glasses with side-shields.
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: butyl-rubber
Minimum layer thickness: 0,3 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,2 mm
Break through time: 45 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of 3-METHOXYBUTANOL:
-Conditions for safe storage, including any incompatibilities
Keep container tightly closed in a dry and well-ventilated place.
Store in cool place.



STABILITY and REACTIVITY of 3-METHOXYBUTANOL:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Incompatible materials:
No data available
-Hazardous decomposition products:
Other decomposition products - No data available



SYNONYMS:
3-Methoxybutan-1-ol
3-METHOXY-1-BUTANOL
2517-43-3
3-Methoxybutanol
1-Butanol, 3-methoxy-
Methoxybutanol
1-Butanol, 3-methoxy-, (-)-
SJ995B41AO
NSC-65580
1,3-butylene glycol 3-monomethyl ether
CCRIS 8976
3-methoxybutyl alcohol
EINECS 219-741-8
NSC 65580
UNII-SJ995B41AO
AI3-24920
3-methoxy-butanol
NSC65580
Methoxybutanol; 98%
3-methoxybutane-1-ol
3-methoxy-butan-1-ol
EC 219-741-8
DSSTox_CID_24812
DSSTox_RID_80495
NCIOpen2_000145
DSSTox_GSID_44812
SCHEMBL28708
3-Methoxy-1-butanol, 99%
3-METHOXYBUTANOL
CHEMBL3186019
DTXSID0044812
CHEBI:189086
Tox21_301623
MFCD00002931
AKOS015903512
CS-W013686
NCGC00256054-01
CAS-2517-43-3
FT-0615965
M0109
EN300-94645
D77758
A877677
J-015851
Q27289241
F0001-0848
3-methoxy-1-butanol
3-methoxybutanol
1-butanol, 3-methoxy
methoxybutanol
ccris 8976
1-butanol, 3-methoxy-
r, 3-methoxy-butanol
3-methoxybutane-1-ol
3-methoxybutyl alcohol
(3R)-3-methoxybutan-1-ol
(3S)-3-methoxybutan-1-ol
1,3-Butylene glycol 3-monomethyl ether
1-Butanol, 3-Methoxy-
3-Methoxybutan-1-ol
3-Methoxybutanol
3-Methoxybutyl alcohol
NSC 65580
Methoxybutanol
3-Methoxybutanol
3-methoxy-1-butano
3-Methoxy-1-butanol
3-Methoxybutan-1-ol
3-METHOXY-1-BUTANOL
3-METHOXY-N-BUTANOL
3-methoxybutan-1-ol
1-Butanol,3-methoxy-
1-butanol, 3-methoxy-
(3R)-3-methoxybutan-1-ol
(3S)-3-methoxybutan-1-ol
1,3-butyleneglycol monomethyl ether
Methoxy-1-buta
Methoxybutanol
3-Methoxybutanol
3-methoxy-1-butano
3-methoxybutan-1-ol
3-METHOXY-1-BUTANOL
3-METHOXY-N-BUTANOL
1-Butanol,3-methoxy-
3-Methoxy-1-butanol>3-Methoxy-1-butanol,99%

3-METHYL-3-PENTANOL
A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. The 3-METHYL-3-PENTANOL molecule contains a total of 20 bond(s) There are 6 non-H bond(s), 2 rotatable bond(s), 1 hydroxyl group(s) and 1 tertiary alcohol(s).3-Methyl-3-Pentanol appears as a colorless to pale yellow liquid with a powerful leafy odor. This product is used as a flavor ingredient in the food industry.It can be prepared by reacting ethylmagnesium bromide with methyl acetate in the so-called Grignard reaction using dried diethyl ether or tetrahydrofuran as solvent.It can be prepared also by reacting ethylmagnesium bromide with butanone in the same conditions already mentioned.Causes changes in brain circulation (hemorrhage, thrombosis, etc.), tetany, and dyspnea in intraperitoneal lethal-dose studies of rats; Human inhalation of 270 mg/m3 causes cough; [RTECS] Safe when used as a flavoring agent in food; [EFSA] May cause irritation; Harmful by ingestion; [Sigma-Aldrich MSDS] See "3-Pentanol."3-Methyl-pentanol-(3) [German]; Methyldiaethylcarbinol [German]; Methyldiethylcarbinol; 3-Methylpentan-3-ol; 3-Pentanol, 3-methyl-; [ChemIDplus] Diethyl methyl carbinol; [Sigma-Aldrich MSDS] UN1987C-6-based green leaf volatiles (GLVs) are signal molecules to herbivorous insects and play an important role in plant–herbivore interactions. How isomerization of GLVs affects insect’s olfactory response has been rarely tested. In laboratory and field experiments, we examined the effect of hexanol isomers on olfactory orientation of the spiraling whitefly, Aleruodicus dispersus Russell, a highly polyphagous pest. In a Y-tube oflactometer, we found that (±)-2-hexanol, 3-methyl-3-pentanol and 3,3-dimethyl-1-butanol significantly attracted female A. dispersus. The trap captures of 3,3-dimethyl-1-butanol were significantly more than that of (±)-2-hexanol and 3-methyl-3-pentanol, and its optimum concentration was 1 μ1/ml. We suggest that the anthropogenic compound 3,3-dimethyl-1-butanol can be exploited as a parakairomone (synthetic analogues of kairomone) to monitor and control adult A. dispersus.For the optical resolution of racemic 1-phenylethylamine in 3-methyl-3-pentanol, subtilisin was reformulated by lyophilization with buffer salts. The amide synthesis activity of subtilisin in organic solvent was compared with the hydrolysis activity in aqueous buffer when different buffer species and their concentrations were used in lyophilization. The enzyme activity in organic solvent showed a different pattern from that of the hydrolysis depending upon the species and the concentrations of buffers. Morphology of the reformulated subtilisin was examined by scanning electron microscopy (SEM). The porosity of reformulated subtilisin particles increased up to the optimal buffer concentrations for the amide synthesis in organic solvent. Glassy looks and decrease in porosity developed at high (i.e. above the optimal) buffer concentrations appear to affect the decrease in the synthetic activity in organic media.A THERAPEUTIC COMPOSITION COMPRISING AS AN ACTIVE MUSCLE RELAXING AND TRANQUILIZING AGENT 3-METHYL-3PHENTANOL CARBAMATE IN A PHARMACEUTICAL CARRIER, SAID CARBAMATE BEING PRESENT IN THE AMOUNT OF ABOUT 50 TO 800 MG. PER UNIT DOSE OF SAID COMPOSITION.3-METHYL-3-PENTANOL CARBAMATE COMPOSI- TIONS HAVING MUSCLE RELAXING AND TRANQUILIZING ACTION Bengt Olof Melander, Stockholm, and Gunnar Hanshoii, Sodertalge, Sweden, assignors to A/B Kabi, Stockholm, Sweden, a corporation of Sweden No Drawing. Filed Nov. 17, 1958, Ser. No. 774,091 Claims priority, application Sweden Nov. 23, 1957 4 Claims. (Cl. 167-65) wherein R and R are alkyl substituents having a combined total of 4 carbon atoms and R is a 1 to 2 carbon alkyl group.3 Example IV 10.2 g. of B-methyl-Z-pentanol in 50 ml. of dry ethyl ether are added dropwise to 8 g. of carbamyl chloride in 25 ml. of dry ethyl ether at C. while stirring. The reaction mixture is left overnight, treated with distilled water, dried and evaporated to dryness. The residue is recrystallized from petroleum ether leaving 3-methyl-3- pentanol-carbamate with the MP. 54-55 C.Example VII 8 g. of carbamyl chloride are added to a cooled mixture of 10.2 g. of 3-methyl-3-pentanol and 50 ml. of chloroform. To this solution are added subsequently 5 g. of dry calcium carbonate at such a rate that the temperature does not exceed 0 C. After stirring for 2 hours at room temperature the precipitate formed is filtered oil, the chloroform solution treated with distilled water and dried over magnesium sulfate. The solvent is evaporated and the residue recrystallized from petroleum ether leaving 3-methyl-3-' entanol-carbamate with the M.P. 54-55" C.Example X g. of 3-methyl-3-penten-3-ol carbamate (prepared from the corresponding alcohol by the procedure as described in Example I) are dissolved in 100 ml. of methanol and subjected to hydrogenation in the presence of 0.2 g. of platinum oxide catalyst at a temperature of 40 C. and a hydrogen pressure of 1 kg/cmfi. After completed reaction the catalyst is removed and the methanol is driven oil. Upon recrystallization from pctroleum ether resulting 3-methyl-3-pentanol carbamate has the M1. 54-55" C.Example Xl According to the method of Example X, hydrogenation of 3-methyl-3-penten-3-ol carbamate yields 3-methyl- 3-pentanol carbamate with the MP. 54-55 C.Example: XIII According to the method of Example XII, (1,1-diethylpr0pyl)-phenyl carbonate and ammonia are reacted to The 3-methyl-3-pentanol-carbamate formed has .4 form 3-ethy1-3 pentano1-carbamate with the MP. 8l- 82C.G. 3-methyl-3-pentanol-carbamate Lactose granulation Magnesium stearate -e 5 are mixed well together and compressed into tablets Weighing 250 mg. (diameter 9 mm.) and containing 100 mg. of the carbamate.Example XVL-Coated tablets A paste is prepared of Kg. Starch 1 Water 5 A mixture of Kg. 3-methyl-3-pentanol-carbamate 20 Lactose 14 Starch 4 is granulated with the starch paste, dried, screened and mixed, with 1 kg. of magnesium stearate.G. 3-methyl-3-pentanolcarbamate a- 20 Polyethylene glycol (average mol. wt. 600) 17 Polyethylene glycol (average mol. wt. 1000) 33 and the solution is mixed with G. Sorbitan monooleate 2.7 Polyoxyethylene sorbitan monooleate 2.7 Hydrogenated coconut oil (melted) 223 Water 1.6.Example XX .Capsules A mixture is prepared containing equal parts by weight of 3-methyl-3-pentanol-carbamate and lactose. This mixture is then filled 400 mg. per capsule into standard clear gelatin capsules and after closing, the capsules are preferably dusted with talc or cornstarch. The resulting capsules contain per dosage unit 200 mg. of the carbamate.In the foregoing Examples XV to XX it will be understood that 3-ethyl-3-pentanol-carbamate or 2-methyl-2- pentanol-carbamate can be substituted for the 3-methyl-3- pentanol-carbamate as active component, and that the amounts of active component can be suitably varied within the range of to 800 mg., and preferably to 400 mg. per dosage unit.A therapeutic composition comprising as an active muscle relaxing and tranquilizing agent 3-methyl-3- pentanol carbamate in a pharmaceutical carrier, said carbamate being present in the amount of about 50 to 800 mg. per unit dose of said composition.The 2D chemical structure image of 3-METHYL-3-PENTANOL is also called skeletal formula, which is the standard notation for organic molecules. The carbon atoms in the chemical structure of 3-METHYL-3-PENTANOL are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide the carbon atom with four bonds.The 3D chemical structure image of 3-METHYL-3-PENTANOL is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them. The radius of the spheres is therefore smaller than the rod lengths in order to provide a clearer view of the atoms and bonds throughout the chemical structure model of 3-METHYL-3-PENTANOL.For a better understanding of the chemical structure, an interactive 3D visualization of 3-METHYL-3-PENTANOL is provided here.The 3-METHYL-3-PENTANOL molecule shown in the visualization screen can be rotated interactively by keep clicking and moving the mouse button. Mouse wheel zoom is available as well – the size of the 3-METHYL-3-PENTANOL molecule can be increased or decreased by scrolling the mouse wheel.The information of the atoms, bonds, connectivity and coordinates included in the chemical structure of 3-METHYL-3-PENTANOL can easily be identified by this visualization. By right-clicking the visualization screen, various other options are available including the visualization of van der Waals surface and exporting to a image file.The 3-Pentanol, 3-methyl-, with the CAS registry number 77-74-7, is also known as Diethylmetylcarbinol. Its EINECS number is 201-053-4. This chemical's molecular formula is C6H14O and molecular weight is 102.17. What's more, its systematic name is 3-methylpentan-3-ol. Its classification code is Drug / Therapeutic Agent. It is used as intermediate and solvent for organic synthesis. It should be sealed and stored at room temperature.Physical properties of 3-Pentanol, 3-methyl- are: (1)ACD/LogP: 1.57; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.57; (4)ACD/LogD (pH 7.4): 1.57; (5)ACD/BCF (pH 5.5): 9.22; (6)ACD/BCF (pH 7.4): 9.22; (7)ACD/KOC (pH 5.5): 170.7; (8)ACD/KOC (pH 7.4): 170.7; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.415; (14)Molar Refractivity: 31.34 cm3; (15)Molar Volume: 125.1 cm3; (16)Polarizability: 12.42×10-24cm3; (17)Surface Tension: 26 dyne/cm; (18)Density: 0.816 g/cm3; (19)Flash Point: 46.1 °C; (20)Enthalpy of Vaporization: 42 kJ/mol; (21)Boiling Point: 122.4 °C at 760 mmHg; (22)Vapour Pressure: 6.65 mmHg at 25°C.Preparation: this chemical can be prepared by 3-methyl-pentane at the temperature of 60 °C. This reaction will need reagent p-nitroperbenzoic acid and solvent CHCl3. The yield is about 84%.3-Pentanol, 3-methyl- can be prepared by 3-methyl-pentane at the temperature of 60 °CUses of 3-Pentanol, 3-methyl-: it can be used to produce 2-(1-ethyl-1-methyl-propoxy)-tetrahydro-pyran at the ambient temperature. It will need reagent TaCl5-SiO2 and solvent CH2Cl2 with the reaction time of 10 min. The yield is about 76%.3-Pentanol, 3-methyl- can be used to produce 2-(1-ethyl-1-methyl-propoxy)-tetrahydro-pyran at the ambient temperatureWhen you are using this chemical, please be cautious about it as the following:This chemical is flammable. It is harmful if swallowed. When using it, you must avoid contact with eyes. Use Classification Food additives -> Flavoring Agents Properties Related Categories Alcohols, Building Blocks, C2 to C6, Chemical Synthesis, Organic Building Blocks, More... Quality Level 100 assay 98% refractive index n20/D 1.418 (lit.) bp 123 °C (lit.) mp −38 °C (lit.) density 0.824 g/mL at 25 °C (lit.) storage temp. room temp SMILES string CCC(C)(O)CC InChI 1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3 InChI key FRDAATYAJDYRNW-UHFFFAOYSA-N 3-Methyl-3-pentanol is an aroma-active alcohol that occurs naturally in pandan leaves, red pepper and fruit of Lycii fructus. 3-Pentanol, 3-methyl- Formula: C6H14O Molecular weight: 102.1748 IUPAC Standard InChI: InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3 Download the identifier in a file. INChI Trust 2011 Certified Logo IUPAC Standard InChIKey: FRDAATYAJDYRNW-UHFFFAOYSA-N CAS Registry Number: 77-74-7 Chemical structure: C6H14O This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Other names: 3-Methyl-3-pentanol; 3-Methylpentan-3-ol; Methyldiaethylcarbinol; Methyldiethylcarbinol; 3-Methyl-pentanol-(3); Methyl-3 pentanol-3 Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Condensed phase thermochemistry data References Notes Other data available: Gas phase thermochemistry data Phase change data Reaction thermochemistry data Gas phase ion energetics data IR Spectrum Mass spectrum (electron ionization) Gas Chromatography Options: Switch to calorie-based units 3-Methyl-3-pentanol Properties Melting point:−38 °C(lit.) alpha 22 º (c=8,6N HCl) Boiling point:123 °C(lit.) Density 0.824 g/mL at 25 °C(lit.) refractive index n20/D 1.418(lit.) Flash point:115 °F pka15.38±0.29(Predicted) Water Solubility slightly Decomposition 176-178 ºC BRN 1731456 CAS DataBase Reference77-74-7(CAS DataBase Reference) EWG's Food Scores1 FDA UNIISR4551FEKB NIST Chemistry Reference3-Pentanol, 3-methyl-(77-74-7) EPA Substance Registry System3-Methyl-3-pentanol (77-74-7) 3-methylpentan-3-ol is a member of the class of compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). Thus, 3-methylpentan-3-ol is considered to be a fatty alcohol lipid molecule. 3-methylpentan-3-ol is soluble (in water) and an extremely weak acidic compound (based on its pKa). 3-methylpentan-3-ol is a fruity, green, and leafy tasting compound and can be found in a number of food items such as green bell pepper, pepper (c. annuum), orange bell pepper, and red bell pepper, which makes 3-methylpentan-3-ol a potential biomarker for the consumption of these food products. Water Solubility 26.4 g/L logP 1.54 ALOGPS logP 1.58 logS -0.59 ALOGPS pKa (Strongest Acidic) 19.03 pKa (Strongest Basic) -1 Physiological Charge 0 Hydrogen Acceptor Count 1 Hydrogen Donor Count 1 Polar Surface Area 20.23 Ų Rotatable Bond Count 2 Refractivity 31.11 m³·mol⁻¹ Polarizability 12.71 ų Number of Rings 0 Bioavailability Yes Rule of Five Yes Ghose Filter No Veber's Rule Yes MDDR-like Rule No Chemical Formula C6H14O IUPAC name 3-methylpentan-3-ol InChI Identifier InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3 InChI Key FRDAATYAJDYRNW-UHFFFAOYSA-N Isomeric SMILES CCC(C)(O)CC Average Molecular Weight 102.1748 Monoisotopic Molecular Weight 102.10446507 You can still convert the following datas into molecular structure: (1)SMILES: OC(C)(CC)CC (2)Std. InChI: InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3 (3)Std. InChIKey: FRDAATYAJDYRNW-UHFFFAOYSA-N
3-NITROBENZENESULFONIC ACID SODIUM SALT
DESCRIPTION:

3-Nitrobenzenesulfonic acid sodium salt is used in the synthesis of quinoline.
3-Nitrobenzenesulfonic acid sodium salt is easily soluble in water, soluble in ethanol, ethyl ether, and copper acetone.
3-Nitrobenzenesulfonic acid sodium salt has oxidizing properties in neutral and alkaline media, and is resistant to acid, alkali and hard water.



CAS NUMBER: 127-68-4

EC NUMBER: 204-857-3

MOLECULAR FORMULA: 3-(NO2)C6H4SO3Na

MOLECULAR WEIGHT: 225.15



DESCRIPTION:

The solubility in water at 25°C is 25 g/100 ml.
3-Nitrobenzenesulfonic acid sodium salt is a chemical compound with the molecular formula C6H4NO5SNa.
3-Nitrobenzenesulfonic acid sodium salt is classified as an aromatic sulfonic acid salt and belongs to the family of nitrobenzenesulfonic acids.
3-Nitrobenzenesulfonic acid sodium salt finds applications in various industries due to its properties as a versatile intermediate compound.
One of the significant applications of 3-Nitrobenzenesulfonic acid sodium salt is in the production of dyes and pigments.

3-Nitrobenzenesulfonic acid sodium salt serves as a building block for various colorants and contributes to the development of vibrant and stable colors in textiles, printing inks, and paints.
3-Nitrobenzenesulfonic acid sodium salt is used as a reagent or standard in analytical methods, particularly in titration and colorimetric assays.
3-Nitrobenzenesulfonic acid sodium salt's specific chemical properties make it suitable for specific tests and determinations in laboratory settings.

3-Nitrobenzenesulfonic acid sodium salt acts as a useful intermediate in the synthesis of pharmaceuticals and fine chemicals.
3-Nitrobenzenesulfonic acid sodium salt can be employed in the preparation of various biologically active compounds.
3-Nitrobenzenesulfonic acid sodium salt may be used as an additive to modify electrodeposition characteristics, improve adhesion, or control the thickness of the plated metal.
3-Nitrobenzenesulfonic acid sodium salt is utilized as a precursor to create novel molecules or explore new chemical reactions.

3-Nitrobenzenesulfonic acid sodium salt's sulfonic acid functional group provides unique reactivity and can be modified for diverse applications.
The chemical structure of 3-Nitrobenzenesulfonic acid sodium salt consists of a benzene ring (C6H4) with a nitro group (NO2) and a sulfonic acid group (SO3H) attached to it.
The sodium ion (Na+) acts as a counterion to balance the negative charge of the sulfonic acid group, resulting in the salt formation.
3-Nitrobenzenesulfonic acid sodium salt can be synthesized through the sulfonation of 3-nitrobenzene with concentrated sulfuric acid (H2SO4).

3-Nitrobenzenesulfonic acid sodium salt is typically a light yellow to orange crystalline powder.
3-Nitrobenzenesulfonic acid sodium salt is soluble in water and other polar solvents.
3-Nitrobenzenesulfonic acid sodium salt can be used as a standard or reagent in analytical methods.

3-Nitrobenzenesulfonic acid sodium salt is used in the synthesis of various dyes and pigments.
3-Nitrobenzenesulfonic acid sodium salt may serve as a building block in organic synthesis for the preparation of other compounds.
3-Nitrobenzenesulfonic acid sodium salt is a reagent in the synthesis of azetidinyl ketolides for treatment of susceptible and multidrug resistant community-acquired respiratory tract infections.



USAGES:

-used as an anti whitening additive for vat dyes
-used as a color and light protective agent for ground color discharge printing such as copper salt, reactive dye and naftor dye
-used as an agent for repairing embossed cloth
-used as a color light protector during steaming after reactive dye printing
-Used as shade protectant for pad dyeing and steaming with reactive dyes
-used as a white ground protective agent for reducing dye yarn fabric during scouring
-Rust remover for ships and nickel remover for electroplating (90% yellow and white are available)
-3-Nitrobenzenesulfonic acid sodium salt can also be used to prepare vanillin



USAGE AREAS:

-Used as antireduction agent
-Used in chemical industry
-Used in electrical/electronics industry
-Used in photographic industry
-Used in textile processing industries



APPLICATION FIELDS:

-as an anti-dyeing agent for dye intermediates and sulfur dyes
-as a dye color-forming protective agent.
-organic pigments
-medicine and chemical industry
-flavor and fragrance industry
-electroplating auxiliaries



SPECIFICATIONS:

-Appearance: White Amorphous Particles or Powder
-Content%≥: 95
-Calcium salt%≤: 0.6
-PH(30% water solution): 7~9
-Moisture%≤: 3.0
-Impurities%≤: 0.2



PRODUCT INFORMATIONS:

-CAS number: 127-68-4
-EC index number: 609-048-00-2
-EC number: 204-857-3
-Hill Formula: C₆H₄NNaO₅S
-Chemical formula: 3-(NO₂)C₆H₄SO₃Na
-Molar Mass: 225.16 g/mol



PHYSICAL AND CHEMICAL PROPERTIES:

-Density: 0.45 g/cm3 (20 °C)
-Flash point: 100 °C
-Ignition temperature: 355 °C
-Melting Point: 350 °C (decomposition)
-pH value: 8 (50 g/l, H₂O, 23 °C)
-Bulk density: 450 kg/m3
-Solubility: 200 g/l



SPECIFICATIONS:

-Assay (acidimetric after ion exchange): ≥ 92.0 %
-Water (K. F.): ≤ 5.0 %
-Identity (IR): passes test
-CAS Min %: 98.5
-CAS Max %: 100.0
-Melting Point: 350.0°C
-Color: Yellow
-pH: 6 to 10 (1% aq. soln.)
-Flash Point: >100°C
-Infrared Spectrum: Authentic
-Assay Percent Range: 98.5% min. (HPLC)
-Formula Weight: 225.15
-Percent Purity: 99%
-Physical Form: Crystalline Powder



CHEMICAL IDENTIFIER:

-Linear Formula: O2NC6H4SO3Na
-MDL Number: MFCD00007490
-EC No.: 204-857-3
-IUPAC Name: sodium; 3-nitrobenzenesulfonate
-SMILES: C1=CC(=CC(=C1)S(=O)(=O)[O-])[N+](=O)[O-].[Na+]
-InchI Identifier: InChI=1S/C6H5NO5S.Na/c8-7(9)5-2-1-3-6(4-5)13(10,11)12;/h1-4H,(H,10,11,12);/q;+1/p-1
-InchI Key: LJRGBERXYNQPJI-UHFFFAOYSA-M




STORAGE:

3-Nitrobenzenesulfonic acid sodium salt should be sealed and stored in a dry and cool place below 35℃.



SYNONYM:

Ludigo
Nacan
Sodium 3-nitrophenylsulfonate
Sodium m-nitrobenzenesulfonate
SODIUM 3-NITROBENZENESULFONATE
Sodium 3-nitrobenzenesulphonate
3-Nitrobenzenesulfonic acid sodium salt
Sodium m-nitrobenzenesulfonate
Benzenesulfonic acid, 3-nitro-, sodium salt
Nitrol S
UNII-1F11SXJ4C6
Tiskan
3-Nitrobenzenesulfonic acid, sodium salt
MFCD00007490
sodium m-nitrobenzene sulfonate
1F11SXJ4C6
m-Nitrobenzenesulfonic acid sodium salt
Nitrobenzen-m-sulfonan sodny
m-nitrobenzene sulfonic acid sodium salt
Ludigol F,60
Benzenesulfonic acid, m-nitro-, sodium salt (8CI)
3-Nitrobenzenesulfonic acid sodium salt
HSDB 5614
Benzenesulfonic acid, m-nitro-, sodium salt
NSC 9795
Nitrobenzen-m-sulfonan sodny [Czech]
m-Nitrobenzenesulfonic acid, sodium salt
Resist Salt
Benzenesulfonic acid, 3-nitro-, sodium salt (1:1)
C6H4NNaO5S
DSSTox_CID_7048
DSSTox_RID_78292
DSSTox_GSID_27048
sodium 3-nitrophenylsulfonate
Sodium3-nitrobenzenesulphonate
sodium m-nitrobezene sulfonate
sodium;3-nitrobenzenesulfonate
SCHEMBL340713
sodium m-nitrobenzenesulphonate
sodium 3-nitro-benzenesulfonate
sodium 3-nitrobenzene sulfonate
sodium m-nitrobenzene-sulphonate
CHEMBL3188704
DTXSID2027048
sodium 3-nitrobenzene sulphonate
sodium 3-nitro-benzene sulfonate
3-nitrobenzene sulfonate sodium salt
Tox21_200902
Sodium 3-nitrobenzenesulfonate, 98%
3-nitrobenzensulfonic acid sodium salt
AKOS015900868
3-nitro-phenylsulfonic acid sodium salt
3-nitro benzenesulfonic acid sodium salt
3-nitro-benzenesulfonic acid sodium salt
3-nitrobenzene sulfonic acid sodium salt
m-nitrobenzene sulphonic acid sodium salt
NCGC00258456-01
3-nitrobenzene sulphonic acid sodium salt
AC-11596
AS-12915
DB-041868
FT-0616236
N0141
W-108378
Q27252345
F1113-0115
SMNBS
3-Nitrobenzenesulfonic Acid Sodium Salt
Meta Nitrobenzene Sulphonic Acid
MNBSA
Benzenesulfonicacid, 3-nitro-, sodium salt (9CI)
Benzenesulfonic acid, m-nitro-, sodium salt(8CI)
3-Nitrobenzenesulfonic acid sodium salt
Ludigol
Nacan
Nitrol S
Sodium m-nitrobenzenesulfonate
m-Nitrobenzenesulfonicacid sodium salt
3-Nitrobenzenesulfonicacidsodiumsalt
benzenesulfonic acid, 3-nitro-, sodium salt (1:1)
Natrium-3-nitrobenzolsulfonat
Sodium 3-Nitrobenzenesulfonate
4-Chloro-3-nitrobenzenesulfonic acid, sodium salt
sodium 4-chloro-3-nitrobenzenesulfonate
Sodium 3-nitro-4-chlorobenzenesulfonate
4-Chloro-3-nitrobenzenesulfonic acid sodium salt
sodium;4-chloro-3-nitrobenzenesulfonate
Sodium 4-chloro-3-nitrobenzenesulphonate
Benzenesulfonic acid, 4-chloro-3-nitro-, sodium salt
EINECS 241-680-0
Benzenesulfonic acid, 4-chloro-3-nitro-, sodium salt (1:1)
SCHEMBL176738
SODIUM 4-CHLORO-3-NITROBENZENE-1-SULPHONATE
4ZNE7E5C39
DTXSID5066245
POUGKTDTYSAMAT-UHFFFAOYSA-M
MFCD00007496
AKOS002376253
sodium 4-chloro-3-nitrobenzensulfonate
sodium4-chloro-3-nitrobenzenesulfonate
sodium,4-chloro-3-nitrobenzenesulfonate
sodium 4-chloro-3-nitro-benzenesulfonate
AC-11461
AS-14860
Sodium 1-chloro-2-nitrobenzene-4-sulfonate
CS-0333824
FT-0618082
I10076
A812215
W-107835
4-chloro-3-nitro-benzenesulfonate;Sodium 3-nitro-4-chlorobenzenesulfonate











3-SULFOALANINE
3-sulfoalanine is an amino acid generated by oxidation of cysteine, whereby a thiol group is fully oxidized to a sulfonic acid/sulfonate group.
3-sulfoalanine, also known as Cysteic acid or Cysteate, belongs to the class of organic compounds known as alpha amino acids.
3-sulfoalanine exists in all living species, ranging from bacteria to humans.

CAS Number: 498-40-8
EC Number: 207-861-3
Molecular Formula: C3H7NO5S
Molecular Weight (g/mol): 169.15

Synonyms: Cysteic Acid, 3-Sulfoalanine, DL-CYSTEIC ACID, 2-amino-3-sulfopropanoic acid, 13100-82-8, cysteate, beta-Sulfoalanine, Alanine, 3-sulfo-, 3024-83-7, Cysteinic acid, Cepteic acid, Cipteic acid, Cysteric acid, A3OGP4C37W, CHEBI:21260, Cysteinesulfonate, 2-amino-3-sulfopropanoate, L-Cysteate, UNII-A3OGP4C37W, cysteinsaure, Cepteate, Cipteate, Cysterate, NSC 254030, NSC-254030, L-Cysteic acid, 8, 3-Sulfoalanine, (L)-, 2-Amino-3-sulfopropionate, CYSTEIC ACID [MI], CYSTEIC ACID, DL-, CHEMPACIFIC41266, SCHEMBL44030,m2-amino-3-sulfopro-panoic acid, CHEMBL1171434, 2-azanyl-3-sulfo-propanoic acid, BDBM85473, DTXSID40862048, XVOYSCVBGLVSOL-UHFFFAOYSA-N, BBL100099, MFCD00065088, NSC254030, STL301905, AKOS005174455, 3-Sulfoalanine (H-DL-Cys(O3H)-OH), LS-04435, FT-0627746, FT-0655399, FT-0683826, C-9550, EN300-717791, A820275, Q2823250, Z1198149799, InChI=1/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9, 13100-82-8 [RN], 2-amino-3-sulfopropanoic acid, 3024-83-7 [RN], 3-Sulfoalanin [German] [ACD/IUPAC Name], 3-Sulfoalanine [ACD/IUPAC Name], 3-Sulfoalanine [French] [ACD/IUPAC Name], A3OGP4C37W, a-Amino-b-sulfopropionic Acid, Alanine, 3-sulfo- [ACD/Index Name], CYA, Cysteic Acid, Cysteic acid (VAN), CYSTEIC ACID, D-, CYSTEIC ACID, DL-, CYSTEIC ACID, L-, DL-cysteic acid, L-Cysteic Acid, UNII:A3OGP4C37W, α-amino-β-sulfopropionic acid, 2-Amino-3-sulfopropanoate [ACD/IUPAC Name], 2-Amino-3-sulfopropionate, Cepteate, Cipteate, Cysteinesulfonate, Cysterate, (R)-2-Amino-3-sulfopropanoic acid, (S)-2-Amino-3-sulfopropanoic acid, [13100-82-8] [RN], 207-861-3 [EINECS], 2-Amino-3-sulfopropionic acid, 35554-98-4 [RN], 3-Sulfoalanine, (L)-, 3-sulfoalanine|alanine, 3-sulfo-, Alanine, 3-sulfo-, L-, C-9550, Cepteic acid, Cipteic acid, cysteate, cysteinate, cysteine sulfonic acid, CYSTEINESULFONIC ACID, Cysteinic acid, Cysteins??ure, Cysteric acid, DL-CYSTEICACID, L-Alanine, 3-sulfo- [ACD/Index Name], L-Cysteate, L-Cysteic acid, 8, MFCD00007524, MFCD00065088 [MDL number], β-Sulfoalanine

3-sulfoalanine also known as 3-sulfo-l-alanine is the organic compound with the formula HO3SCH2CH(NH2)CO2H.
3-sulfoalanine is often referred to as Cysteic acid, which near neutral pH takes the form −O3SCH2CH(NH3+)CO2−.

3-sulfoalanine is an amino acid generated by oxidation of cysteine, whereby a thiol group is fully oxidized to a sulfonic acid/sulfonate group.
3-sulfoalanine is further metabolized via 3-sulfolactate, which converts to pyruvate and sulfite/bisulfite.
The enzyme L-3-sulfoalanine sulfo-lyase catalyzes this conversion.

3-sulfoalanine is a biosynthetic precursor to taurine in microalgae.
By contrast, most taurine in animals is made from cysteine sulfinate.

3-sulfoalanine and cysteine sulfinic acid (metabolic intermediates from taurine biosynthesis in the brain) significantly reduce [3H]taurine uptake in cultured neurons, whereas cysteine, isethionic acid, cysteamine, and cystamine exhibit no alterations in taurine transport.

3-sulfoalanine, also known as Cysteic acid or Cysteate, belongs to the class of organic compounds known as alpha amino acids.
These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).

An amino sulfonic acid that is the sulfonic acid analogue of cysteine.
3-sulfoalanine is a very strong basic compound (based on 3-sulfoalanine pKa).

3-sulfoalanine exists in all living species, ranging from bacteria to humans.
Within humans, 3-sulfoalanine participates in a number of enzymatic reactions.
In particular, 3-sulfoalanine can be converted into taurine through 3-sulfoalanine interaction with the enzyme cysteine sulfinic acid decarboxylase.

In addition, 3-sulfoalanine can be converted into taurine through 3-sulfoalanine interaction with the enzyme glutamate decarboxylase 1.
In humans, 3-sulfoalanine is involved in taurine and hypotaurine metabolism.

3-sulfoalanine, also known as Cysteic acid or Cysteate, belongs to the class of organic compounds known as alpha amino acids.
These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).

3-sulfoalanine is a very strong basic compound (based on 3-sulfoalanine pKa).
3-sulfoalanine exists in all living species, ranging from bacteria to humans.

L-3-sulfoalanine is a beta-sulfoalanine.
3-sulfoalanine is an amino acid with a C-terminal sulfonic acid group which has been isolated from human hair oxidized with permanganate.
3-sulfoalanine occurs normally in the outer part of the sheep's fleece, where the wool is exposed to light and weather.

3-sulfoalanine, also known as 3-sulfo-1-alanine, is an organic compound with the formula HO3SCH2CH(NH2)CO2H.
3-sulfoalanine is often called Cysteic acid, and at near-neutral pH 3-sulfoalanine takes the form -O3SCH2CH(NH3+)CO2-.

An amino acid produced by the oxidation of cysteine, where the thiol group is completely oxidized to a sulfonic acid/sulfonate group.
3-sulfoalanine is further metabolized via 3-sulfolactic acid and converted to pyruvate and sulfite/bisulfite.

The enzyme L-3-sulfoalanine sulfolyase catalyzes this conversion.
3-sulfoalanine is the biosynthetic precursor of taurine in microalgae.
In contrast, most taurine in animals is made from cysteine ​​sulfinic acid.

Fmoc-L-3-sulfoalanine is an Fmoc protected cysteine derivative potentially useful for proteomics studies, and solid phase peptide synthesis techniques.
Cysteine is versatile amino acid involved with many biological processes, including the formation of disulfide bonds - a critical component of protein structure.
3-sulfoalanine could be useful as an unusual amino acid analog to aid in the deconvolution of protein structure and function.

3-sulfoalanine is an amino sulfonic acid that is the sulfonic acid analogue of cysteine.
3-sulfoalanine has a role as an animal metabolite.
3-sulfoalanine is an alanine derivative, an amino sulfonic acid, a carboxyalkanesulfonic acid, a cysteine derivative and a non-proteinogenic alpha-amino acid.

3-sulfoalanine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).

3-sulfoalanine is a natural product found in Phaseolus vulgaris and Homo sapiens with data available.

3-sulfoalanine can be readily oxidized, where the main degradation products are mixed disulfides within one molecule, disulfide cross-links between molecules, and sulfenic, sulfinic, and 3-sulfoalanine.
Transition metals such as Cu2+ and Fe3+ can catalyze the formation of disulfide bonds.

As an example, human fibroblast growth factor (FGF-1) forms dimers as the result of intermolecular disulfides by copper-catalyzed oxidation.
These metal-catalyzed reactions generally can occur without a neighboring thiol group.

In the absence of transition metals the formation of new intramolecular or intermolecular disulfide bridges generally requires a nearby free thiol group that breaks apart the existing native disulfide bridge and then the free thiol can reoxidize to form the disulfide bridge.
Since this reaction requires a free thiol anion (pKa is ∼9) an increase in the solution pH will result in an increase in formation of mixed disulfide.

However, the pKa values for 3-sulfoalanine can vary depending on the proximity of other ionizing groups in the tertiary structure.
These interactions are primarily electrostatic in nature and since the ionization of these neighboring groups changes with the pH the pKa values of the 3-sulfoalanine residues will be a function of pH.

As an example, the thiol pKa in papain for the active site Cys 25 has been estimated to be 4.1 at pH 6 and 8.4 at pH 9.
This observation suggests that at pH 6 there is a His residue with positive charge in close proximity to 3-sulfoalanine 25, whereas at pH 9 the electrostatic interactions are dominated by close negatively charged residues such as Asp or Glu residues.

The effects of local electrostatic environments on thiol pKa values and disulfide exchange have been discussed by Snyder, Cennerazzo, Karalis, and Field (1981).
Ion pairing with His residues has also been proposed for the decrease in the Cys pKa values.

3-sulfoalanine has been used to couple to hydrophobic labels like Cyanine and Rhodamine dyes and other hydrophobic residues to increase their solubility in water.
As di- or tripeptide a further increase of hydrophilicity can be achieved

3-sulfoalanine has been used to couple to hydrophobic labels like Cyanine and Rhodamine dyes and other hydrophobic residues to increase their solubility in water.
As di- or tripeptide a further increase of hydrophilicity can be achieved.

3-sulfoalanine can be coupled in SPPS by standard phosphoniumor uranium-based coupling reagents.
In high throughput technologies for DNA sequencing and genomics charge-modified dye-labelled
dideoxynucleoside-5’-triphosphates were synthesized for “direct-load” applications in DNA.

L-Cysteine and L-3-sulfoalanine were synthesized by paired eletrolysis method.
A high purity over 98% and high yield over 90% of both products were gained.

When current density was 7 A/dm2 and concentration of L-cysteine was 0.6 mol/dm3, the highest current efficiency of anode and cathode was achieved.
Total current efficiency was over 180%.

The cyclic voltammetry behaviors of hydrobromic acid and cystine showed that a typical EC reaction took place in the anodic cell.
The anode reaction and successive chemical reaction accelerated each other to get a high speed and current efficiency.

L-3-sulfoalanine is the L-enantiomer of 3-sulfoalanine.
3-sulfoalanine has a role as an Escherichia coli metabolite and a human metabolite.

3-sulfoalanine is a 3-sulfoalanine, an amino sulfonic acid, a L-alanine derivative, a L-cysteine derivative and a non-proteinogenic L-alpha-amino acid.
3-sulfoalanine is a conjugate acid of a L-3-sulfoalanine(1-).

L-3-sulfoalanine is a beta-sulfoalanine.
3-sulfoalanine is an amino acid with a C-terminal sulfonic acid group which has been isolated from human hair oxidized with permanganate.
3-sulfoalanine occurs normally in the outer part of the sheep's fleece, where the wool is exposed to light and weather.

Uses of 3-sulfoalanine:
An amino acid with a C-terminal sulfonic acid group which has been isolated from human hair oxidized with permanganate.
3-sulfoalanine occurs normally in the outer part of the sheep's fleece, where the wool is exposed to light and weather.

Application of 3-sulfoalanine:
Internal standard for amino acid analysis.

Biochem/physiol Actions of 3-sulfoalanine:
L-3-sulfoalanine is a sulfur containing aspartate analogue that may be used as a competitive inhibitor of the bacterial aspartate: alanine antiporter (AspT) exchange of aspartate and in other aspartate biological systems.
L-3-sulfoalanine is used in monomeric surfactant development.

L-3-sulfoalanine is an oxidation product of Cysteine.
L-3-sulfoalanine, an analogue of cysteine sulfinic acid, may be used in studies of excitatory amino acids in the brain, such as those that bind to cysteine sulfinic acid receptors.
L-3-sulfoalanine is a useful agonist at several rat metabotropic glutamate receptors (mGluRs).

Pharmacology and Biochemistry of 3-sulfoalanine:

Human Metabolite Information:

Cellular Locations:
Mitochondria

Handling and storage of 3-sulfoalanine:

Conditions for safe storage, including any incompatibilities:

Storage conditions:
Tightly closed.
Dry.

Storage class:
Storage class (TRGS 510): 11: Combustible Solids

Stability and reactivity of 3-sulfoalanine:

Reactivity:

The following applies in general to flammable organic substances and mixtures:
In correspondingly fine distribution, when whirled up a dust explosion potential may generally be assumed.

Chemical stability:
3-sulfoalanine is chemically stable under standard ambient conditions (room temperature).

Possibility of hazardous reactions:
No data available

Conditions to avoid:
no information available

Incompatible materials:
Strong oxidizing agents

First aid measures of 3-sulfoalanine:

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.

Firefighting measures of 3-sulfoalanine:

Suitable extinguishing media:
Water Foam Carbon dioxide (CO2) Dry powder

Unsuitable extinguishing media:
For 3-sulfoalanine no limitations of extinguishing agents are given.

Special hazards arising from 3-sulfoalanine:
Carbon oxides
Nitrogen oxides (NOx)
Sulfur oxides
Combustible.

Development of hazardous combustion gases or vapours possible in the event of fire.

Advice for firefighters:
In the event of fire, wear self-contained breathing apparatus.

Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.

Accidental release measures of 3-sulfoalanine:

Personal precautions, protective equipment and emergency procedures:

Advice for non-emergency personnel:
Avoid inhalation of dusts.
Evacuate the danger area, observe emergency procedures, consult an expert.

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.
Avoid generation of dusts.

Identifiers of 3-sulfoalanine:
CAS Number:
13100-82-8 (D/L)
35554-98-4 (D)
498-40-8 (L)

ChEBI: CHEBI:17285
ChemSpider: 65718
DrugBank: DB03661
ECHA InfoCard: 100.265.539
EC Number: 207-861-3
MeSH: Cysteic+acid
PubChem CID: 25701

UNII:
A3OGP4C37W (D/L)
YWB11Z1XEI (D)
M6W2DJ6N5K (L)

CompTox Dashboard (EPA): DTXSID40862048
InChI: InChI=1S/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
Key: XVOYSCVBGLVSOL-REOHCLBHSA-N
InChI=1/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
SMILES: C(C(C(=O)O)N)S(=O)(=O)O

Synonym(s): (R)-2-Amino-3-sulfopropionic acid
Linear Formula: HO3SCH2CH(NH2)CO2H·H2O
CAS Number: 23537-25-9
Molecular Weight: 187.17
Beilstein: 3714036
MDL number: MFCD00149544
PubChem Substance ID: 24858207
NACRES: NA.26

CAS: 498-40-8
Molecular Formula: C3H7NO5S
Molecular Weight (g/mol): 169.15
MDL Number: MFCD00007524
InChI Key: XVOYSCVBGLVSOL-UHFFFAOYNA-N
PubChem CID: 72886
ChEBI: CHEBI:17285
IUPAC Name: 2-amino-3-sulfopropanoic acid
SMILES: NC(CS(O)(=O)=O)C(O)=O

Properties of 3-sulfoalanine:
Chemical formula: C3H7NO5S
Molar mass: 169.15 g·mol−1
Appearance: White crystals or powder
Melting point: Decomposes around 272 °C
Solubility in water: Soluble

Quality Level: 200
Assay: ≥99.0% (T)
form: powder or crystals
optical activity: [α]20/D +7.5±0.5°, c = 5% in H2O
technique(s): LC/MS: suitable
color: white to faint yellow
mp: 267 °C (dec.) (lit.)
solubility: H2O: soluble
application(s): peptide synthesis
SMILES string: [H]O[H].N[C@@H](CS(O)(=O)=O)C(O)=O
InChI: 1S/C3H7NO5S.H2O/c4-2(3(5)6)1-10(7,8)9;/h2H,1,4H2,(H,5,6)(H,7,8,9);1H2/t2-;/m0./s1
InChI key: PCPIXZZGBZWHJO-DKWTVANSSA-N

Molecular Weight: 169.16 g/mol
XLogP3-AA: -4.5
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 3
Exact Mass: 169.00449350 g/mol
Monoisotopic Mass: 169.00449350 g/mol
Topological Polar Surface Area: 126Ų
Heavy Atom Count: 10
Complexity: 214
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 3-sulfoalanine:
Color: White
Quantity: 1 g
Formula Weight: 169.15
Percent Purity: ≥98.0% (T)
Physical Form: Crystalline Powder
Chemical Name or Material: L-Cysteic Acid

Related Products of 3-sulfoalanine:
(R)-(-)-2,2-Dimethyl-1,3-dioxolane-4-methanol
(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxylic Acid Methyl Ester
[2R-[2a,6a,7b(R*)]]-7-[[[[(1,1-Dimethylethoxy)carbonyl]amino]phenylacetyl]amino]-3-methylene-8-oxo-5-thia-1-azabicyclo[4.2.0]octane-2-carboxylic Acid 5-Oxide
(S)-4',7-Dimethyl Equol
(3a'R,4'S,5'S,6a'S)-5'-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]hexahydro-N-[(1R)-2-hydroxy-1-phenylethyl]-5,5-dimethyl-spiro[1,3-dioxane-2,2'(1'H)-pentalene]-4'-carboxamide

Names of 3-sulfoalanine:

IUPAC name:
(R)-2-Amino-3-sulfopropanoic acid

Regulatory process names:
L-cysteic acid
L-cysteic acid

Other names:
3-Sulfo-l-alanine

Other identifiers:
498-40-8
3-THIOPROPIONIC ACID
3-Thiopropionic Acid contains both carboxylic acid and thiol groups.
3-Thiopropionic Acid is a colorless oil and derived from the addition of hydrogen sulfide to acrylic acid.
3-Thiopropionic Acid that is propanoic acid carrying a sulfanyl group at position 3.

CAS: 107-96-0
MF: C3H6O2S
MW: 106.14
EINECS: 203-537-0

3-Thiopropionic Acid is an organic compound.
3-Thiopropionic Acid exists as a colourless liquid that demonstrates solubility in both water and organic solvents.
As a sulfur-containing carboxylic acid and a derivative of propionic acid, 3-Mercaptopropionic acid serves as a crucial precursor for the synthesis of various organic compounds, making 3-Thiopropionic Acid invaluable across scientific and industrial applications.
In scientific research, this compound finds widespread usage as a reagent in organic synthesis and in the production of proteins and other biomolecules.
3-Thiopropionic Acid also functions as a chelating agent, adept at binding metal ions within aqueous solutions, and plays a vital role as a stabilizing agent in polymer production.

3-Thiopropionic Acid Chemical Properties
Melting point: 15-18 °C (lit.)
Boiling point: 110-111 °C/15 mmHg (lit.)
Density: 1.218 g/mL at 25 °C (lit.)
Vapor pressure: 0.04 mm Hg ( 20 °C)
Refractive index: n20/D 1.492(lit.)
FEMA: 4587 | 3-MERCAPTOPROPIONIC ACID
Fp: 201 °F
Storage temp.: Store below +30°C.
Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
Pka: pK1:;pK2:10.84(SH) (25°C)
Form: Crystalline Powder, Crystals, and/or Chunks
Color: White
Specific Gravity: 1.218
PH: 2 (120g/l, H2O, 20℃)
Odor: sulfurous roasted
Odor Type: sulfurous
Explosive limit: 1.60%(V)
Water Solubility: soluble
Sensitive: Air Sensitive & Hygroscopic
JECFA Number: 1936
BRN: 773807
Stability: Air Sensitive, Hygroscopic
InChIKey: DKIDEFUBRARXTE-UHFFFAOYSA-N
LogP: -2.3 at 22℃
CAS DataBase Reference: 107-96-0(CAS DataBase Reference)
NIST Chemistry Reference: 3-Thiopropionic Acid (107-96-0)
EPA Substance Registry System: 3-Thiopropionic Acid (107-96-0)

Synonyms
3-MERCAPTOPROPIONIC ACID
107-96-0
3-Mercaptopropanoic acid
3-Sulfanylpropanoic acid
3-Thiopropionic acid
3-Thiopropanoic acid
beta-Mercaptopropionic acid
Mercaptopropionic acid
Propanoic acid, 3-mercapto-
3MPA
2-Mercaptoethanecarboxylic acid
beta-Thiopropionic acid
Hydracrylic acid, 3-thio-
Propionic acid, 3-mercapto-
Thiohydracrylic acid
beta-Mercaptopropanoic acid
NSC 437
.beta.-Thiopropionic acid
UNII-B03TJ3QU9M
.beta.-Mercaptopropionic acid
C3H6O2S
Propionic acid, 3-mercpato-
3-Thiolpropanoic acid
3-thiohydracrylic acid
3-Mercaptopropionicacid
HSDB 5381
EINECS 203-537-0
3-mercapto-propionic acid
Mercaptopropionic acid, 3-
BRN 0773807
B03TJ3QU9M
.beta.-Mercaptopropanoic acid
AI3-26090
CHEMBL358697
DTXSID8026775
CHEBI:44111
NSC-437
EC 203-537-0
4-03-00-00726 (Beilstein Handbook Reference)
beta-Mercaptopropionate
3 Mercaptopropionic Acid
MFCD00004897
3-mercaptopropionsyre
BMPA
DEAMINO CYSTEINE
ss--Thiopropionic acid
betamercaptopropionic acid
3- mercaptopropionic acid
3-mercapto-propanoic acid
Propionic acid, mercapto-
ss--Mercaptopropanoic acid
ss--Mercaptopropionic acid
3-Sulfanylpropanoic acid #
SCHEMBL7289
USAF E-5
3-Mercaptopropanoic acid, 9CI
DTXCID106775
NSC437
3-Mercaptopropionic acid, 98%
FEMA NO. 4587
3-Mercaptopropionic acid, >=99%
AMY27767
BCP16636
STR01222
Tox21_200194
BDBM50121953
MERCAPTOPROPIONIC ACID [INCI]
STL281859
Thiopropionic acid; 3-Thiopropanoic acid; beta-Mercaptopropionic acid
AKOS000121541
AC-4722
AT21041
SB66313
3-MERCAPTOPROPIONIC ACID [HSDB]
propionic acid, 3-mercapto-methyl ester
NCGC00248556-01
NCGC00257748-01
BP-21405
CAS-107-96-0
LS-124729
LS-124730
FT-0615955
FT-0658630
M0061
3-Mercaptopropionic acid, >=99.0% (HPLC)
EN300-19579
3-Dimethylamino-2-methylpropylchloridehydrochloride
A801785
J-512742
Q11751618
F2191-0215
Z104474322
InChI=1/C3H6O2S/c4-3(5)1-2-6/h6H,1-2H2,(H,4,5
68307-97-1
4,4-DITHIODIMORPHOLINE
4,4-Dithiodimorpholine molecule contains a total of 30 atom(s).
4,4-Dithiodimorpholine is a white or similar white crystal.


CAS Number: 103-34-4
EC Number: 203-103-0
MDL Number: MFCD00023319
Molecular Formula: C8H16N2O2S2



4,4'-DITHIODIMORPHOLINE, 103-34-4, Morpholine, 4,4'-dithiobis-, Sulfasan, 4,4-Dithiodimorpholine, Sulfasan R, Accel R, 4,4'-Dithiomorpholine, Morpholine disulfide, Morpholino disulfide, 4,4'-Dithiobismorpholine, Dimorpholine disulfide, Dimorpholino disulfide, Bismorpholino disulfide, Deovulc M, Sanfel R,
Dithiobismorpholine, Morpholinodisulfide, Vanax A, Disulfide, dimorpholino-, Usaf ek-t-6645, Usaf B-17, Dimorpholine N,N'-disulfide, N,N-Dithiodimorpholine, 4,4'-Dithiobis(morpholine), N,N'-Bismorpholine disulfide, N,N'-Dimorpholine Disulfide, Morpholine, 4,4'-dithiodi-, N,N'-Dithiodimorfolin, DITHIODIMORPHOLINE, 4-(morpholin-4-yldisulfanyl)morpholine, NSC 65239, Dithiobis(morpholine), N,N'-Dithiodimorpholine, DTXSID8026698, M786P489YF, NSC65239,
NSC-65239, Vulnoc, DTXCID706698, Di(morpholin-4-yl) disulphide, 4-(4-Morpholinyldisulfanyl)morpholine, CAS-103-34-4, Morpholine, N,N'-disulfide-,
CCRIS 8923, HSDB 5351, EINECS 203-103-0, 4,4/'-Dithiodimorpholine, BRN 0126214, UNII-M786P489YF, AI3-08625, Sulfazan R, 4-(morpholinodisulfanyl)morpholine, Dimorpholinodisulfide, Naugex SD-1, Akrochem accelerator R, Morpholine,4'-dithiodi-, 1,2-dimorpholinodisulfane, Morpholine,4'-dithiobis-, 4,4'-dithio-dimorpholine, N,N'-DimorpholineDisulfide, EC 203-103-0, Bis(4-morpholinyl)disulfide, Morpholine, N,N'-disulfide, N,N'-Dithiobis(morpholine), NCIOpen2_003134, 4-27-00-00613 (Beilstein Handbook Reference), 4,4'-Dimorpholine disulphide, SCHEMBL137538, CHEMBL582932, HLBZWYXLQJQBKU-UHFFFAOYSA-, MORPHOLINE N,N'-DISULFIDE, DITHIODIMORPHOLINE, 4,4'-, 4-morpholin-4-yldisulfanylmorpholine, Tox21_201775, Tox21_303110, BDBM50414924, MFCD00023319, AKOS015897388, WLN: T6N DOTJ ASS-AT6N DOTJ, 4,4'-DITHIODIMORPHOLINE [MI], 4,4'-DITHIODIMORPHOLINE [HSDB], 4-(4-Morpholinyldisulfanyl)morpholine #, NCGC00249116-01, NCGC00257082-01, NCGC00259324-01, AS-57709, CS-0196466, D0282, FT-0657982, NS00006501, E78171, Q27283591, InChI=1/C8H16N2O2S2/c1-5-11-6-2-9(1)13-14-10-3-7-12-8-4-10/h1-8H2, N,N'-Dimorpholine disulfide, N,N'-Dithiobis(morpholine), 4-(Morpholin-4-yldisulfanyl)morpholine, Morpholine, 4,4'-dithiobis-, Morpholine, 4,4'-dithiobis-, Accel R, Bismorpholino disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobis(morpholine), Morpholine disulfide, Morpholine, 4,4'-dithiodi-, Morpholino disulfide, N,N'-Bismorpholine disulfide, N,N'-Dithiodimorpholine, Sulfasan, Sulfasan R, USAF EK-T-6645, USAF B-17, 4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, N,N'-Dithiodimorfolin, Sulfazan R, 4,4'-Dimorpholine disulphide, Akrochem accelerator R, Dimorpholine N,N'-disulfide, Morpholine, N,N'-disulfide, Naugex SD-1, Vanax A, Deovulc M, NSC 65239, Sanfel R, di(morpholin-4-yl) disulphide, N,N'-Dithiobismorpholine, N,N'-Dithiodimorpholine, Morpholine disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, 4,4'-DITHIOBIS(MORPHOLINE), 4,4'-Dithiomorpholine, Bismorpholino disulfide, Di(morpholin-4-yl) disulphide, Dimorpholine disulfide, Dimorpholino disulfide, Morpholine, 4,4'-dithiobis-, Accel R, Bismorpholino disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobis(morpholine), Morpholine disulfide, Morpholine, 4,4'-dithiodi-, Morpholino disulfide, N,N'-Bismorpholine disulfide, N,N'-Dithiodimorpholine,
Sulfasan, Sulfasan R, USAF EK-T-6645, USAF B-17, 4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, N,N'-Dithiodimorfolin, Sulfazan R, 4,4'-Dimorpholine disulphide, Akrochem accelerator R, Dimorpholine N,N'-disulfide, Morpholine, N,N'-disulfide, Naugex SD-1, Vanax A, Deovulc M, NSC 65239, Sanfel R,
di(morpholin-4-yl) disulphide, N,N'-disulfide-Morpholine, DTDM, Dimorpholine N,N'-disulfide, Sulfasan R,, Morpholine, 4',4'-dithiodimorpholine, 4,4-dithiomorpholine, 4,4-dithiodimorpholine, morpholine disulfide, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide), 4,4'-dithio dimorpholine, 4,4'-dithiodimorpholine, 4,4'-dithiodimorpholinesulfasan(r)r, morpholinen,n'-disulfide, n,n'-dimorpholinedisulfide, n,n'-dithiobis(morpholine), vanaxa, vanaxafinegrind, vanaxarodform, 4,4'-dimorpholinedisulfide, 4,4'-dithiomorpholine, dtdm, dithiomorpholine, dimorpholinen,n'-disulfide, 4-(4-morpholinyldisulfanyl)morpholine, 4,4'-dithiobis(morpholine), 4,4'-dithiobis-morpholin, 4,4'-dithiobismorpholine, 4,4'-dithiobis-morpholine, 4,4'-dithiodi-morpholin, 4,4'-disulfanediyldimorpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, Rubber Accelerator DTDM, Rubber Vulcanizing Agent DTDM, Vulcanising Agent DTDM, 203-103-0, 4,4'-disulfanediyl-bis-morpholine, 4,4'-Disulfanediyldimorpholine, 4,4'-Dithiobis[morpholine], 4Mmorpholin-4-yldisulfanylmorpholine, accelr, deovulcm, DIMORPHOLINE DISULFIDE, Dimorpholine N,N'-disulfide, dimorpholinodisulfide, dithiodimorpholine, DTDM, EINECS 203-103-0, MFCD00023319, Morpholine N,N'-disulfide, Morpholine, 4,4'-dithiobis-, Morpholine, N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), N,N'-dithio-bis-morpholine, sanfelr, SULFASAN(R) R, Sulfazan R, usafb-17, VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, vulnoc,
SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4Mmorpholin-4-yldisulfanylmorpholine, DTDM, 4,4'-d, accelr, vulnoc, VANAX A, sanfelr, Accel R, deovulcm, usafb-17, USAF B-17, SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4Mmorpholin-4-yldisulfanylmorpholine
4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, Accel R, Bismorpholino disulfide, Deovulc M, Dimorpholine N,N'-disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobismorpholine, Morpholine disulfide, Morpholine, 4,4'-dithiobis-, Morpholine, 4,4'-dithiodi-, Morpholine, N,N'-disulfide-, Morpholino disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, N,N-Dithiodimorpholine, Sanfel R, Sulfasan, Sulfasan R, Vanax A, Vulnoc, DTDM, Morpholine disulfide, 4,4'-Dithiodimorpholin, SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4,4'-DITHIODIMORPHOLINE, Morpholine,4,4′-dithiobis-, Morpholine,4,4′-dithiodi-, 4,4′-Dithiobis[morpholine], 4,4′-Dithiodimorpholine, Morpholine disulfide, Sulfasan R, Sulfasan, N,N′-Dithiodimorpholine, N,N′-Bismorpholine disulfide, Bismorpholino disulfide, Accel R, Morpholinodisulfide, N,N′-Dimorpholinyl disulfide, Sanfel R, Vanax A, Bismorpholine disulfide, N,N′-Dithiobis[morpholine], Deovulc M, Di(4-morpholinyl) disulfide, Rhenocure M/G, Vulnoc R, Sulfasan DTDM, DTDM, Actor R, NSC 65239, Rhenocure M, Nocmaster R 80E, DTDM 80, Rhenogran DTDM 80, Sulphasan R, TT 106, 39393-19-6, 186983-49-3, 1081512-50-6, dimorpholinodisulfide, deovulcm, N,N-Dimorpholine Disulfide, MFCD00023319, 4,4-Dithiobis[morpholine], dithiodimorpholine, vulnoc, accelr, N,N-Dithiobis(morpholine), Sulfazan R, usafb-17, 4,4-Dithiodimorpholine, N,N-dithio-bis-morpholine, sanfelr, EINECS 203-103-0, Morpholine, 4,4-dithiobis-, 4,4-disulfanediyl-bis-morpholine, Dimorpholine N,N-disulfide, VANAX A, Morpholine, N,N-disulfide, DTDM, 4,4-Disulfanediyldimorpholine, dtdm, DTDM, vanaxa, VANAX A, vanaxarodform, SULFASAN(R) R, VANAX A RODFORM, vanaxafinegrind, dithiomorpholine, VANAX A FINE GRIND, 4,4-dithiomorpholine, morpholine disulfide, 4,4'-dithiomorpholine, 4,4-dithiodimorpholine, 4,4'-dithiodimorpholine, Rubber Accelerator DTDM, 4,4'-dithiodi-morpholin, morpholinen,n'-disulfide, 4,4'-dithiobismorpholine, 4,4'-dithio dimorpholine, 4,4'-dithiobis-morpholin, 4,4'-dithiobis-morpholine, Morpholine N,N'-disulfide, n,n'-dimorpholinedisulfide, 4,4'-dimorpholinedisulfide, dimorpholinen,n'-disulfide, n,n'-dithiobis(morpholine), 4,4'-dithiobis(morpholine), N,N'-DITHIOBIS(MORPHOLINE), N,N'-DIMORPHOLINE DISULFIDE, di(morpholin-4-yl) disulphide, 4,4'-disulfanediyldimorpholine, di(morpholin-4-yl) disulphide, 4,4'-dithiodimorpholinesulfasan(r)r, 4Mmorpholin-4-yldisulfanylmorpholine, 4-(4-morpholinyldisulfanyl)morpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide)
Morpholine,4,4'-dithiodi- (6CI,7CI,8CI), 4,4'-Dithiobis[morpholine], 4,4'-Dithiodimorpholine, Accel R, Actor R, Bismorpholine disulfide, Bismorpholino disulfide, DTDM, Deovulc M, Di(4-morpholinyl) disulfide, Morpholine disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, N,N'-Dimorpholinyl disulfide, N,N'-Dithiobis[morpholine], N,N'-Dithiodimorpholine, NSC 65239, Nocmaster R 80E, Rhenocure M, RhenocureM/G, Sanfel R, Sulfasan, Sulfasan DTDM, Sulfasan R, Vanax A, Vulnoc R, Rubber accelerator DTDM, 4',4'-dithiodimorpholine, 4,4-dithiomorpholine, 4,4-dithiodimorpholine, morpholine disulfide, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide), 4,4'-dithio dimorpholine, 4,4'-dithiodimorpholine, 4,4'-dithiodimorpholinesulfasan(r)r, morpholinen,n'-disulfide, n,n'-dimorpholinedisulfide, n,n'-dithiobis(morpholine), vanaxa, vanaxafinegrind, vanaxarodform, 4,4'-dimorpholinedisulfide, 4,4'-dithiomorpholine, dtdm, dithiomorpholine, dimorpholinen,n'-disulfide, 4-(4-morpholinyldisulfanyl)morpholine, 4,4'-dithiobis(morpholine), 4,4'-dithiobis-morpholin, 4,4'-dithiobismorpholine, 4,4'-dithiobis-morpholine, 4,4'-dithiodi-morpholin, 4,4'-disulfanediyldimorpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, Rubber Accelerator DTDM, Rubber Vulcanizing Agent DTDM, Vulcanising Agent DTDM,



4,4-Dithiodimorpholine is suitable for vulcanizing temperature between 140°C to 200°C.
4,4-Dithiodimorpholine has no blooming and pollution and is easy to disperse in sizing materials with good processability.
4,4-Dithiodimorpholine improves reducibility resistance of vulcanizing rubber.


4,4-Dithiodimorpholine exhibits excellent thermal and anti-oxidative performance to produce dynamic heat resistance in rubber products.
4,4-Dithiodimorpholine helps to reduce heat build-up property in NR and SBR.
Store 4,4-Dithiodimorpholine in a cool and dry place with good ventilation.


4,4-Dithiodimorpholine molecule contains a total of 30 atom(s).
There are 16 Hydrogen atom(s), 8 Carbon atom(s), 2 Nitrogen atom(s), 2 Oxygen atom(s), and 2 Sulfur atom(s).
A chemical formula of 4,4-Dithiodimorpholine can therefore be written as: C8H16N2O2S2


The chemical formula of 4,4-Dithiodimorpholine shown above is based on the molecular formula indicating the numbers of each type of atom in a molecule without structural information, which is different from the empirical formula which provides the numerical proportions of atoms of each type.
The chemical formula of 4,4-Dithiodimorpholine is the basis of stoichiometry in chemical equations, i.e., the calculation of relative quantities of reactants and products in chemical reactions.


The law of conservation of mass dictates that the quantity of each element given in the chemical formula of 4,4-Dithiodimorpholine does not change in a chemical reaction.
Thus, each side of the chemical equation must represent the same quantity of any particular element based on the chemical formula of 4,4-Dithiodimorpholine.


4,4-Dithiodimorpholine is the offering body of the sulphur.
4,4-Dithiodimorpholine will release a percentage of 27 active sulphur in the temperature of vulcanization.
4,4-Dithiodimorpholine 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.


4,4-Dithiodimorpholine, synonymous with DTDM and Vulcanizing Agent DTDM, is a sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure systems.
4,4-Dithiodimorpholine is a white crystline powder or granule that is primarily used in the production of synthetic rubbers and adhesives.


4,4-Dithiodimorpholine is a vulcanizing agent and promoter of natural and synthetic rubber, it can release the sulphur in the vulcanizing temperature.
4,4-Dithiodimorpholine is a white or similar white crystal.
4,4-Dithiodimorpholine is an organic compound that has been used in a variety of scientific research applications.


4,4-Dithiodimorpholine will produce a high connecting effect to the rubber, part or whole replace the sulphur, so make the active sulphur gain an ideal physical machine function.
That makes up half effective structure rubber tesist not only fatigue but also oxidation.


According to 4,4-Dithiodimorpholine’s special chemical structure in the performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.
4,4-Dithiodimorpholine is non flammable.


4,4-Dithiodimorpholine, synonymous with DTDM and Vulcanizing Agent DTDM, is a sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure systems.
4,4-Dithiodimorpholine is a white crystline powder or granule that is primarily used in the production of synthetic rubbers and adhesives.


4,4-Dithiodimorpholine is a white, solid, crystalline compound with a molecular weight of 256.35 g/mol.
4,4-Dithiodimorpholine is insoluble in water, but soluble in polar organic solvents.
4,4-Dithiodimorpholine is a versatile reagent and has been used in a variety of organic and inorganic syntheses.


4,4-Dithiodimorpholine does not spray, does not pollute, and is easy to disperse in the rubber compound, and has good processing performance.
4,4-Dithiodimorpholine releases high-efficiency vulcanization rubber with high-efficiency vulcanization properties, which can significantly improve the resistance of vulcanizates.


4,4-Dithiodimorpholine can decompose morpholine free radicals with amine antioxidants in the rubber compound, which can make the vulcanized rubber have excellent heat and oxidation resistance.
4,4-Dithiodimorpholine has excellent thermal properties and is ideal for the manufacture of dynamic heat-resistant rubber products.


4,4-Dithiodimorpholine can reduce the heat-generating NR and SNR and is an ideal rubber vulcanizing agent.
With the increase of people's environmental protection concepts and health concerns, it has been found that the vulcanizing agents 4,4-Dithiodimorpholine and thiuram products will cleave at the vulcanization temperature to release secondary amino-based molecular fragments, which can be combined with the nitroso donor to produce carcinogens.


Nitrosamines, so the production and application of vulcanizing agents 4,4-Dithiodimorpholine and thiurams are subject to the limits and warnings of European and American countries and environmental regulations.
At present, the new vulcanizing agent DTDC (N, N-di(ε-caprolactam) disulfide) has attracted international attention due to the fact that it does not produce nitrosamines during vulcanization.


It is considered to be a vulcanizing agent 4,4-Dithiodimorpholine and disulfide or hexasulfurate.
The best alternative to M, replacing the vulcanizing agent 4,4-Dithiodimorpholine with the same amount, without changing the formulation and process of the compound.


4,4-Dithiodimorpholine is white or yellowish needle-like crystal.
A chemical formula of 4,4-Dithiodimorpholine can therefore be written as: C8H16N2O2S2.
4,4-Dithiodimorpholine is white or light yellow crystal (or powder).


4,4-Dithiodimorpholine is white or yellowish needle-like crystal.
4,4-Dithiodimorpholine is a white crystalline or powder.
Specific gravity of 4,4-Dithiodimorpholine is 1.28-1.32.


4,4-Dithiodimorpholine has no poison.
4,4-Dithiodimorpholine is soluble in benzene, alcohol and acetone.
4,4-Dithiodimorpholine is insoluble in water.


The vulcanizing agent 4,4-Dithiodimorpholine can adapt to the vulcanization temperature of 140 °C-200 °C, and the scorch safety is good.
After reaching the normal vulcanization temperature, the vulcanization rate is accelerated, and the vulcanization property is ideal.
4,4-Dithiodimorpholine has excellent thermal properties and is ideal for the manufacture of dynamic heat-resistant rubber products.



USES and APPLICATIONS of 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is used in formulation or re-packing and at industrial sites.
4,4-Dithiodimorpholine is used in the following products: polymers.
Release to the environment of 4,4-Dithiodimorpholine can occur from industrial use: formulation of mixtures and formulation in materials.


4,4-Dithiodimorpholine is used for the manufacture of: rubber products.
4,4-Dithiodimorpholine is used sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure system; provide heat/reversion/aging resistance in NR and synthetic rubbers; non-blooming; excellent storage safety.


4,4-Dithiodimorpholine can be used to improve the anti-retrogradation and anti-thermal aging properties of sulfur vulcanized elastomer.
4,4-Dithiodimorpholine can be used as vulcanizing agent and accelerator for natural rubber and synthetic rubber.
The rubber feed of this product does not spray frost, pollution, discoloration and easy dispersion.


The vulcanizates obtained when used in effective and half-effect vulcanization systems have good heat resistance and aging resistance.
Active sulfur can be released at vulcanization temperature, the effective sulfur content is 27%, the operation is safe, the vulcanization speed is slow when used alone, and the use of thiazole, thiuram and dithiocarbamate can increase the vulcanization speed.


4,4-Dithiodimorpholine is especially suitable for butyl rubber.
4,4-Dithiodimorpholine is produced in the manufacture of tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products.
4,4-Dithiodimorpholine is also used as an asphalt stabilizer for vertical highways.


4,4-Dithiodimorpholine is suitable for natural rubber and synthetic rubber, with the characteristics of heat resistance, fatigue resistance, reduction resistance, no frost spraying, and scorch prevention.
4,4-Dithiodimorpholine can be used in the butyl rubber to produce tyre, butyl inner tube of tire, rubber belt and anti-heat rubber products, it also can be used as pitch stabilizer in the expressway.


4,4-Dithiodimorpholine is widely used in articles resistant to reversion based on NR such as tyre carcasses & ageing resistant articles based on SBR, NBR and EPDM
4,4-Dithiodimorpholine can be used as vulcanizing agent and accelerator of natural rubber and synthetic rubber.


In cross linking reaction, 4,4-Dithiodimorpholine mainly forms mono-sulfur bond.
Release to the environment of 4,4-Dithiodimorpholine can occur from industrial use: as processing aid.
Application of 4,4-Dithiodimorpholine: Sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure system; provide heat/reversion/aging resistance in NR and synthetic rubbers; non-blooming; excellent storage safety.


4,4-Dithiodimorpholine acts as a vulcanizing agent.
Recommended of 4,4-Dithiodimorpholine to be used in rubber.
So many rubber products manufacturers including domestic and overseas pay attention to 4,4-Dithiodimorpholine.


Generally, 4,4-Dithiodimorpholine is used in combination, or sulfenamide or thiazole accelerator is used to adjust the scorch period and vulcanization rate.
4,4-Dithiodimorpholine can be used as a vulcanizing agent and accelerator for natural rubber and synthetic rubber.
4,4-Dithiodimorpholine is mainly used as vulcanization agent and accelerator for natural rubber and artificial rubber.


Under vulcanizing temperature, 4,4-Dithiodimorpholine can decompose active sulfur, whose content is 27%.
4,4-Dithiodimorpholine is primarily used in the synthesis of organosulfur compounds and has also been used in the synthesis of other organic and inorganic compounds such as nitriles, amides, and heterocycles.


The vulcanized rubber has good heat resistance and aging resistance when used in effective and semi-effective vulcanization systems.
At the sulfurization temperature can release the active sulfur, effective sulfur content is 27%, safe operation, when 4,4-Dithiodimorpholine is used alone the sulfurization speed is slow, and thiazole class, thiuram class and dithiocarbamate can be used to increase the sulfurization speed.


4,4-Dithiodimorpholine is especially suitable for butyl rubber, mainly used in the manufacture of tire, butyl inner tube, rubber belt and heat resistant rubber products, also used in highway asphalt stabilizer.
4,4-Dithiodimorpholine does not spray frost, does not pollute, does not change color, easy to disperse.


4,4-Dithiodimorpholine is used suitable for natural rubber and synthetic rubber, with heat resistance, fatigue resistance, anti-reduction, no frost, anti-scorch characteristics.
4,4-Dithiodimorpholine is produced in the manufacture of tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products.



APPLICATION AND CHARACTERISTICS OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is mainly used as vulcanized agent and accelerator for natural rubber and artificial rubber.
Under vulcanizing temperature, 4,4-Dithiodimorpholine can decompose active sulfur, whose content is 27%.
In cross linking reaction, 4,4-Dithiodimorpholine mainly forms monosulphur bond. Its usual use level is 0.5-2 orders.
4,4-Dithiodimorpholine, which has the characteristic of processing safely, is usually used together with such accelerators as thiazoles, thiuram, dithiocarbamates etc.



FEATURES OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is the offering body of the sulphur.
4,4-Dithiodimorpholine will release a percentage of 27 active sulphur in the temperature of vulcanization.
4,4-Dithiodimorpholine will produce a high connecting effect to the rubber, part or whole replace the sulphur, so make the active sulphur gain an ideal physical machine function.

That makes up half effective structure rubber tesist not only fatigue but also oxidation.
According to 4,4-Dithiodimorpholine’s special chemical structure in the performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.
So many rubber products manufacturers including domestic and overseas pay attention to 4,4-Dithiodimorpholine.

Vulcanization temperature, in addition to release active sulphur, so that make the rubber produce a high connecting function, morphlinyl, which has the second amine structure feature.
This kind of free radical can not only resist heat and oxygen, but also delay coking time, so that speed up vulcanization.
So, 4,4-Dithiodimorpholinehas a performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.



CHARACTER OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is a white needle-like crystal.
Relative density 1.32-1.38.
4,4-Dithiodimorpholine is soluble in benzene, carbon tetrachloride, slightly soluble in acetone, gasoline, insoluble in ethanol, ether, insoluble in water.
4,4-Dithiodimorpholine is decomposition in the presence of an inorganic acid or base.
4,4-Dithiodimorpholine is stable storage at room temperature. 4,4-Dithiodimorpholine is non-toxic, fishy.



WHAT IS 4,4-DITHIODIMORPHOLINE AND WHERE IS 4,4-DITHIODIMORPHOLINE FOUND?
4,4-Dithiodimorpholine is used as an accelerator and vulcanizing agent used in rubber products.
4,4-Dithiodimorpholine is also used to protect metals against corrosion and tarnish by acid fumes as well as in toiletry and cosmetic products, hair conditioners, deodorant products and hair dyes.
4,4-Dithiodimorpholine is also found in pharmaceuticals for local anesthetics and antibiotics.
Further research may identify additional product or industrial usages of 4,4-Dithiodimorpholine.



MARKET OVERVIEW OF AND REPORT COVERAGE OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is a chemical compound used as a crosslinking agent in the rubber industry.
4,4-Dithiodimorpholine is primarily used in the production of rubber products to improve their mechanical properties, such as hardness, flexibility, and abrasion resistance.

4,4-Dithiodimorpholine is widely used in the manufacturing of rubber tires, seals, gaskets, conveyor belts, and other rubber products.
The future outlook of the 4,4-Dithiodimorpholine market is promising.
The increasing demand for rubber products across various industries such as automotive, construction, and electronics is driving the growth of this market.

The rising focus on improving the performance and durability of rubber products to meet the stringent quality standards is further boosting the demand for 4,4-Dithiodimorpholine.
Moreover, the growing automotive industry, particularly in emerging economies, is expected to fuel the demand for rubber tires, which, in turn, will drive the demand for 4,4-Dithiodimorpholine.

Additionally, the increasing environmental concerns and regulations regarding the disposal of rubber waste are encouraging manufacturers to seek sustainable and eco-friendly rubber products, further driving the market growth.
The current outlook of the 4,4-Dithiodimorpholine market is positive, with steady growth observed in recent years.

The market is characterized by the presence of several key players who are actively engaged in research and development activities to enhance product performance and expand their market share.
Manufacturers are also focusing on strategic partnerships, collaborations, and acquisitions to strengthen their market position and gain a competitive edge.

Overall, the 4,4-Dithiodimorpholine market is expected to witness significant growth in the coming years.
With increased demand for high-quality and durable rubber products, coupled with technological advancements in the manufacturing process, the market is projected to grow at a CAGR of % during the forecasted period.



PRODUCTION METHOD OF 4,4-DITHIODIMORPHOLINE:
add morpholine, solvent gasoline (or benzene and toluene) and a small amount of water to the reaction kettle.
After stirring evenly, add sulfur monochloride, gasoline and sodium hydroxide solution dropwise into the kettle at the same time, control the temperature below 10 ℃, and add the sodium hydroxide solution slightly before a carbon chloride dropwise.

After dropping, add a certain amount of water and continue stirring for 30min.
The reactants are then pumped out, and the filtrate is separated from the water phase of gasoline and recovered.
The filter cake is added to the centrifuge and washed with water to be neutral.
After removing the water, 4,4-Dithiodimorpholine is dried to obtain the finished product.



SOURCES/USES OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is used as a stain protector for rubber, a vulcanizer (sulfur donor) and accelerator for natural and synthetic rubbers, a fungicide, and a curing agent for poly(fluoroalkoxyphosphazenes).



PURIFICATION METHODS OF 4,4-DITHIODIMORPHOLINE:
Crystallise 4,4-Dithiodimorpholine from hot aqueous dimethylformamide or EtOH.
4,4-Dithiodimorpholine is a fungicide.



CHARACTERISTICS AND APPLICATION OF 4,4-DITHIODIMORPHOLINE:
4,4-Dithiodimorpholine is mainly used as vulcanized agent and accelerator for natural rubber and artificial rubber.
Under vulcanizing temperature, 4,4-Dithiodimorpholine can decompose active sulfur, whose content is 27%.
In cross linking reaction, 4,4-Dithiodimorpholine mainly forms monosulphur bond.

4,4-Dithiodimorpholines usual use level is 0.5-2 orders.
4,4-Dithiodimorpholine, which has the characteristic of processing safely, is usually used together with such accelerators as thiazoles, thiuram, dithiocarbamates etc.



SCIENTIFIC RESEARCH APPLICATIONS OF 4,4-DITHIODIMORPHOLINE:
Chemical Synthesis and Organic Chemistry: 4,4-Dithiodimorpholine's used in the synthesis of thiiranes, contributing to the study of organic chemical reactions.

Toxicology: Research has shown that 4,4-Dithiodimorpholine exhibits significant embryotoxicity, making it a critical subject in studies related to chemical toxicity and environmental safety.

Medical Applications: 4,4-Dithiodimorpholine has potential as a lead compound in treating neoplastic lesions of the cervix by acting on the oncoprotein E6 of human papillomavirus-16.

Antiviral Research: Studies have compared 4,4-Dithiodimorpholine's effects with other compounds in treating HPV-related lesions, contributing to the development of antiviral therapies.

Material Science and Engineering: 4,4-Dithiodimorpholine's effects on the ageing properties of SBS-modified asphalts have been studied, indicating its role in improving the durability of road materials.

Rubber Chemistry: Research has been conducted on 4,4-Dithiodimorpholine'effects on the mechanical properties of EPDM vulcanizate, an important aspect in the field of polymer science and rubber technology.



PHYSICAL and CHEMICAL PROPERTIES of 4,4-DITHIODIMORPHOLINE:
Molecular Weight: 236.4 g/mol
XLogP3-AA: 0.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 3
Exact Mass: 236.06532010 g/mol
Monoisotopic Mass: 236.06532010 g/mol
Topological Polar Surface Area: 75.5Ų
Heavy Atom Count: 14
Formal Charge: 0
Complexity: 143
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: 103-34-4
Formula: C8H16N2O2S2
Molecular weight: 236,35 g/mol
Melting point: 124-125°C
Boiling point: 371.7±52.0 °C(Predicted)
Density: 1.32~1.38g/cm3
vapor pressure: 0.004Pa at 25℃
refractive index: 1.6300 (estimate)
storage temp.: Refrigerator
form: powder to crystaline
pka: 0.78±0.20(Predicted)
color: White to Almost white
Specific Gravity: 1.36
Water Solubility: 215mg/L at 20.2℃
Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N

LogP: 2.67 at 22℃
Indirect Additives used in Food Contact Substances: 4,4'-DITHIODIMORPHOLINE
FDA 21 CFR: 175.105; 177.2600
CAS DataBase Reference: 103-34-4(CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: M786P489YF
NIST Chemistry Reference: Morpholine disulfide(103-34-4)
EPA Substance Registry System: Morpholine, 4,4'-dithiobis- (103-34-4)
Melting point : 124-125°C
Boiling point : 371.7±52.0 °C(Predicted)
density : 1.32~1.38g/cm3
vapor pressure: 0.004Pa at 25℃
refractive index :1.6300 (estimate)
storage temp. : Refrigerator
form : powder to crystaline
pka: 0.78±0.20(Predicted)
color: White to Almost white
Specific Gravity: 1.36

Water Solubility: 215mg/L at 20.2℃
Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
LogP: 2.67 at 22℃
CAS DataBase Reference: 103-34-4(CAS DataBase Reference)
NIST Chemistry Reference: Morpholine disulfide(103-34-4)
EPA Substance Registry System: Morpholine, 4,4'-dithiobis- (103-34-4)
Physical state: powder
Color: white
Odor: No data available
Melting point/freezing point:
Melting point/range: 125,0 °C - OECD Test Guideline 102
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: No data available
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: 0,215 g/l at 20,2 °C
Partition coefficient:
n-octanol/water:
log Pow: 2,67 at 22 °C
Vapor pressure: 0,00004 hPa at 25 °C
Density: 0,4525 g/cm3 at 20 °C
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: No data available

Molecular Formula / Molecular Weight: C8H16N2O2S2 = 236.35
Physical State (20 deg.C): Solid
Storage Temperature: 0-10°C
Condition to Avoid: Heat Sensitive
CAS RN 103-34-4
Reaxys Registry Number: 126214
PubChem Substance ID: 87566980
SDBS (AIST Spectral DB): 10257
Merck Index (14): 3372
MDL Number: MFCD00023319
CAS: 103-34-4
Color: White-Yellow
MDL Number: MFCD00023319
Synonym: N,N′C-Dimorpholine Disulfide, N,N′C-Dithiobis(morpholine)
SMILES: C1COCCN1SSN2CCOCC2
Molecular Weight (g/mol): 236.348
Formula Weight: 236.35
Physical Form: Crystalline Powder

Melting Point: 125°C
Molecular Formula: C8H16N2O2S2
InChI Key: HLBZWYXLQJQBKU-UHFFFAOYSA-N
IUPAC Name: 4-(morpholin-4-yldisulfanyl)morpholine
PubChem CID: 7648
Percent Purity: ≥98.0% (HPLC,N)
Chemical Name or Material: 4,4′-Dithiodimorpholine
CAS No.: 103-34-4
Molecular Formula: C8H16N2O2S2
InChIKeys: InChIKey=HLBZWYXLQJQBKU-UHFFFAOYSA-N
Molecular Weight: 236.35500
Exact Mass: 236.35
EC Number: 203-103-0
UNII: M786P489YF
NSC Number: 65239
DSSTox ID: DTXSID8026698

Color/Form: CRYSTALS|GRAY TO TAN POWDER
Categories: Antioxidants
PSA: 75.54000
XLogP3: 0.73800
Appearance: DryPowder; DryPowder, PelletsLargeCrystals; PelletsLargeCrystals
Density: 1.36 g/cm3 @ Temp: 25 °C
Melting Point: 125 °C
Boiling Point: 371.7ºC at 760 mmHg
Flash Point: 154ºC
Refractive Index: 1.6300 (estimate)
Storage Conditions: Refrigerator
Density: 1.36
Appearance: White Crystal powder
Melting Point: 120 degC min
Ash: 0.30% max
Particle Size: Max- 1.0(63um), 0.50(um)
Oil: 0; 1.0~2.0

Loss on Drying: 0.30% max
Specific gravity: 1.28~1.32
Molecular weight: 236.38
Melting point : 124-125°C
Boiling point : 371.7±52.0 °C(Predicted)
density: 1.32~1.38g/cm3
vapor pressure : 0.004Pa at 25℃
refractive index: 1.6300 (estimate)
storage temp.: Refrigerator
pka: 0.78±0.20(Predicted)
form: powder to crystaline
color: White to Almost white
Specific Gravity: 1.36
Water Solubility: 215mg/L at 20.2℃
Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
LogP: 2.67 at 22℃

Molecular Weight:236.35500
Exact Mass:236.35
EC Number:203-103-0
UNII:M786P489YF
NSC Number:65239
DSSTox ID:DTXSID8026698
Color/Form:CRYSTALS|GRAY TO TAN POWDER
PSA:75.54000
XLogP3:0.73800
Appearance:DryPowder; DryPowder, PelletsLargeCrystals; PelletsLargeCrystals
Density:1.36 g/cm3 @ Temp: 25 °C
Melting Point:125 °C
Boiling Point:371.7ºC at 760 mmHg
Flash Point:154ºC
Refractive Index:1.6300 (estimate)
Storage Conditions: Refrigerator
Melting Point: 124-125°C
Boiling Point: 371.7±52.0 °C at 760 mmHg
Flash Point: 178.6±30.7 °C
Molecular Formula: C8H16N2O2S2
Molecular Weight: 236.355

Density: 1.3±0.1 g/cm3
CAS: 103-34-4
EINECS: 203-103-0
InChI: InChI=1/2C4H9NO.2S/c2*1-3-6-4-2-5-1;;/h2*5H,1-4H2;;/q;;2*-2
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
Molecular Formula: C8H16N2O2S2
Molar Mass: 236.35
Density: 1.32~1.38g/cm3
Melting Point: 124-125°C
Boling Point: 371.7±52.0 °C(Predicted)
Water Solubility: 215mg/L at 20.2℃
Vapor Presure: 0.004Pa at 25℃
Appearance: White powder
Specific Gravity: 1.36
Color: White to Almost white
Merck: 14,3372
pKa: 0.78±0.20(Predicted)
Storage Condition: Refrigerator
Refractive Index: 1.6300 (estimate)
MDL: MFCD00023319
Physical and Chemical Properties: White needle-like crystals.
Fish Odor.



FIRST AID MEASURES of 4,4-DITHIODIMORPHOLINE:
-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.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
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 4,4-DITHIODIMORPHOLINE:
-Personal precautions, protective equipment and emergency procedures:
*Advice for non-emergency personnel:
Ensure adequate ventilation.
-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 4,4-DITHIODIMORPHOLINE:
-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:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of 4,4-DITHIODIMORPHOLINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face 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
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of 4,4-DITHIODIMORPHOLINE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of 4,4-DITHIODIMORPHOLINE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available

4,4'-DITHIODIMORPHOLINE (DTDM)
4,4'-dithiodimorpholine (DTDM) is white or yellowish needle-like crystal.
A chemical formula of 4,4'-dithiodimorpholine (DTDM) can therefore be written as: C8H16N2O2S2.


CAS Number: 103-34-4
EC Number: 203-103-0
MDL Number: MFCD00023319
Molecular Formula: C8H16N2O2S2



Morpholine,4,4′-dithiobis-, Morpholine,4,4′-dithiodi-, 4,4′-Dithiobis[morpholine], 4,4′-Dithiodimorpholine, Morpholine disulfide, Sulfasan R, Sulfasan, N,N′-Dithiodimorpholine, N,N′-Bismorpholine disulfide, Bismorpholino disulfide, Accel R, Morpholinodisulfide, N,N′-Dimorpholinyl disulfide, Sanfel R, Vanax A, Bismorpholine disulfide, N,N′-Dithiobis[morpholine], Deovulc M, Di(4-morpholinyl) disulfide, Rhenocure M/G, Vulnoc R, Sulfasan DTDM, DTDM, Actor R, NSC 65239, Rhenocure M, Nocmaster R 80E, DTDM 80, Rhenogran DTDM 80, Sulphasan R, TT 106, 39393-19-6, 186983-49-3, 1081512-50-6, dimorpholinodisulfide, deovulcm, N,N-Dimorpholine Disulfide, MFCD00023319, 4,4-Dithiobis[morpholine], dithiodimorpholine, vulnoc, accelr, N,N-Dithiobis(morpholine), Sulfazan R, usafb-17, 4,4-Dithiodimorpholine, N,N-dithio-bis-morpholine, sanfelr, EINECS 203-103-0, Morpholine, 4,4-dithiobis-, 4,4-disulfanediyl-bis-morpholine, Dimorpholine N,N-disulfide, VANAX A, Morpholine, N,N-disulfide, DTDM, 4,4-Disulfanediyldimorpholine, dtdm, DTDM, vanaxa, VANAX A, vanaxarodform, SULFASAN(R) R, VANAX A RODFORM, vanaxafinegrind, dithiomorpholine, VANAX A FINE GRIND, 4,4-dithiomorpholine, morpholine disulfide, 4,4'-dithiomorpholine, 4,4-dithiodimorpholine, 4,4'-dithiodimorpholine, Rubber Accelerator DTDM, 4,4'-dithiodi-morpholin, morpholinen,n'-disulfide, 4,4'-dithiobismorpholine, 4,4'-dithio dimorpholine, 4,4'-dithiobis-morpholin, 4,4'-dithiobis-morpholine, Morpholine N,N'-disulfide, n,n'-dimorpholinedisulfide, 4,4'-dimorpholinedisulfide, dimorpholinen,n'-disulfide, n,n'-dithiobis(morpholine), 4,4'-dithiobis(morpholine), N,N'-DITHIOBIS(MORPHOLINE), N,N'-DIMORPHOLINE DISULFIDE, di(morpholin-4-yl) disulphide, 4,4'-disulfanediyldimorpholine, di(morpholin-4-yl) disulphide, 4,4'-dithiodimorpholinesulfasan(r)r, 4Mmorpholin-4-yldisulfanylmorpholine, 4-(4-morpholinyldisulfanyl)morpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide)
Morpholine,4,4'-dithiodi- (6CI,7CI,8CI), 4,4'-Dithiobis[morpholine], 4,4'-Dithiodimorpholine, Accel R, Actor R, Bismorpholine disulfide, Bismorpholino disulfide, DTDM, Deovulc M, Di(4-morpholinyl) disulfide, Morpholine disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, N,N'-Dimorpholinyl disulfide, N,N'-Dithiobis[morpholine], N,N'-Dithiodimorpholine, NSC 65239, Nocmaster R 80E, Rhenocure M, RhenocureM/G, Sanfel R, Sulfasan, Sulfasan DTDM, Sulfasan R, Vanax A, Vulnoc R, Rubber accelerator DTDM, 4',4'-dithiodimorpholine, 4,4-dithiomorpholine, 4,4-dithiodimorpholine, morpholine disulfide, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide), 4,4'-dithio dimorpholine, 4,4'-dithiodimorpholine, 4,4'-dithiodimorpholinesulfasan(r)r, morpholinen,n'-disulfide, n,n'-dimorpholinedisulfide, n,n'-dithiobis(morpholine), vanaxa, vanaxafinegrind, vanaxarodform, 4,4'-dimorpholinedisulfide, 4,4'-dithiomorpholine, dtdm, dithiomorpholine, dimorpholinen,n'-disulfide, 4-(4-morpholinyldisulfanyl)morpholine, 4,4'-dithiobis(morpholine), 4,4'-dithiobis-morpholin, 4,4'-dithiobismorpholine, 4,4'-dithiobis-morpholine, 4,4'-dithiodi-morpholin, 4,4'-disulfanediyldimorpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, Rubber Accelerator DTDM, Rubber Vulcanizing Agent DTDM, Vulcanising Agent DTDM, 4,4'-DITHIODIMORPHOLINE, 103-34-4, Morpholine, 4,4'-dithiobis-, Sulfasan, 4,4-Dithiodimorpholine, Sulfasan R, Accel R, 4,4'-Dithiomorpholine, Morpholine disulfide, Morpholino disulfide, 4,4'-Dithiobismorpholine, Dimorpholine disulfide, Dimorpholino disulfide, Bismorpholino disulfide, Deovulc M, Sanfel R, Dithiobismorpholine, Morpholinodisulfide, Vanax A, Disulfide, dimorpholino-, Usaf ek-t-6645, Usaf B-17, Dimorpholine N,N'-disulfide, N,N-Dithiodimorpholine, 4,4'-Dithiobis(morpholine), N,N'-Bismorpholine disulfide, N,N'-Dimorpholine Disulfide, Morpholine, 4,4'-dithiodi-, N,N'-Dithiodimorfolin, DITHIODIMORPHOLINE, 4-(morpholin-4-yldisulfanyl)morpholine, NSC 65239, Dithiobis(morpholine), N,N'-Dithiodimorpholine, DTXSID8026698, M786P489YF, NSC65239, NSC-65239, Vulnoc, DTXCID706698, Di(morpholin-4-yl) disulphide, 4-(4-Morpholinyldisulfanyl)morpholine, CAS-103-34-4, Morpholine, N,N'-disulfide-, CCRIS 8923, HSDB 5351, EINECS 203-103-0, 4,4/'-Dithiodimorpholine, BRN 0126214, UNII-M786P489YF, AI3-08625, Sulfazan R, 4-(morpholinodisulfanyl)morpholine, Dimorpholinodisulfide, Naugex SD-1, Akrochem accelerator R, Morpholine,4'-dithiodi-, 1,2-dimorpholinodisulfane, Morpholine,4'-dithiobis-, 4,4'-dithio-dimorpholine, N,N'-DimorpholineDisulfide, EC 203-103-0, Bis(4-morpholinyl)disulfide, Morpholine, N,N'-disulfide, N,N'-Dithiobis(morpholine), NCIOpen2_003134, 4-27-00-00613 (Beilstein Handbook Reference), 4,4'-Dimorpholine disulphide, SCHEMBL137538, CHEMBL582932, HLBZWYXLQJQBKU-UHFFFAOYSA-, MORPHOLINE N,N'-DISULFIDE, DITHIODIMORPHOLINE, 4,4'-, 4-morpholin-4-yldisulfanylmorpholine, Tox21_201775, Tox21_303110, BDBM50414924, MFCD00023319, AKOS015897388, WLN: T6N DOTJ ASS-AT6N DOTJ, 4,4'-DITHIODIMORPHOLINE [MI], 4,4'-DITHIODIMORPHOLINE [HSDB], 4-(4-Morpholinyldisulfanyl)morpholine #, NCGC00249116-01, NCGC00257082-01, NCGC00259324-01, AS-57709, CS-0196466, D0282, FT-0657982, NS00006501, E78171, Q27283591, InChI=1/C8H16N2O2S2/c1-5-11-6-2-9(1)13-14-10-3-7-12-8-4-10/h1-8H2, N,N'-Dimorpholine disulfide, N,N'-Dithiobis(morpholine), 4-(Morpholin-4-yldisulfanyl)morpholine, Morpholine, 4,4'-dithiobis-, Morpholine, 4,4'-dithiobis-, Accel R, Bismorpholino disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobis(morpholine), Morpholine disulfide, Morpholine, 4,4'-dithiodi-, Morpholino disulfide, N,N'-Bismorpholine disulfide, N,N'-Dithiodimorpholine, Sulfasan, Sulfasan R, USAF EK-T-6645, USAF B-17, 4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, N,N'-Dithiodimorfolin, Sulfazan R, 4,4'-Dimorpholine disulphide, Akrochem accelerator R, Dimorpholine N,N'-disulfide, Morpholine, N,N'-disulfide, Naugex SD-1, Vanax A, Deovulc M, NSC 65239, Sanfel R, di(morpholin-4-yl) disulphide, N,N'-Dithiobismorpholine, N,N'-Dithiodimorpholine, Morpholine disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, 4,4'-DITHIOBIS(MORPHOLINE), 4,4'-Dithiomorpholine, Bismorpholino disulfide, Di(morpholin-4-yl) disulphide, Dimorpholine disulfide, Dimorpholino disulfide, Morpholine, 4,4'-dithiobis-, Accel R, Bismorpholino disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobis(morpholine), Morpholine disulfide, Morpholine, 4,4'-dithiodi-, Morpholino disulfide, N,N'-Bismorpholine disulfide, N,N'-Dithiodimorpholine, Sulfasan, Sulfasan R, USAF EK-T-6645, USAF B-17, 4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, N,N'-Dithiodimorfolin, Sulfazan R, 4,4'-Dimorpholine disulphide, Akrochem accelerator R, Dimorpholine N,N'-disulfide, Morpholine, N,N'-disulfide, Naugex SD-1, Vanax A, Deovulc M, NSC 65239, Sanfel R, di(morpholin-4-yl) disulphide, N,N'-disulfide-Morpholine, DTDM, Dimorpholine N,N'-disulfide, Sulfasan R,, Morpholine, 4',4'-dithiodimorpholine, 4,4-dithiomorpholine, 4,4-dithiodimorpholine, morpholine disulfide, 4,4-dithiodimorpholine,(4,4-dimorpholine disulphide), 4,4'-dithio dimorpholine, 4,4'-dithiodimorpholine, 4,4'-dithiodimorpholinesulfasan(r)r, morpholinen,n'-disulfide, n,n'-dimorpholinedisulfide, n,n'-dithiobis(morpholine), vanaxa, vanaxafinegrind, vanaxarodform, 4,4'-dimorpholinedisulfide, 4,4'-dithiomorpholine, dtdm, dithiomorpholine, dimorpholinen,n'-disulfide, 4-(4-morpholinyldisulfanyl)morpholine, 4,4'-dithiobis(morpholine), 4,4'-dithiobis-morpholin, 4,4'-dithiobismorpholine, 4,4'-dithiobis-morpholine, 4,4'-dithiodi-morpholin, 4,4'-disulfanediyldimorpholine, 1,1'-[disulfanediylbis(carbonothioyloxy)]diethane, Rubber Accelerator DTDM, Rubber Vulcanizing Agent DTDM, Vulcanising Agent DTDM, 203-103-0, 4,4'-disulfanediyl-bis-morpholine, 4,4'-Disulfanediyldimorpholine, 4,4'-Dithiobis[morpholine], 4Mmorpholin-4-yldisulfanylmorpholine, accelr, deovulcm, DIMORPHOLINE DISULFIDE, Dimorpholine N,N'-disulfide, dimorpholinodisulfide, dithiodimorpholine, DTDM, EINECS 203-103-0, MFCD00023319, Morpholine N,N'-disulfide, Morpholine, 4,4'-dithiobis-, Morpholine, N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), N,N'-dithio-bis-morpholine, sanfelr, SULFASAN(R) R, Sulfazan R, usafb-17, VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, vulnoc, SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4Mmorpholin-4-yldisulfanylmorpholine, DTDM, 4,4'-d, accelr, vulnoc, VANAX A, sanfelr, Accel R, deovulcm, usafb-17, USAF B-17, SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4Mmorpholin-4-yldisulfanylmorpholine, 4,4'-Dithiobis(morpholine), 4,4'-Dithiomorpholine, Accel R, Bismorpholino disulfide, Deovulc M, Dimorpholine N,N'-disulfide, Dimorpholine disulfide, Dimorpholino disulfide, Disulfide, dimorpholino-, Dithiobismorpholine, Morpholine disulfide, Morpholine, 4,4'-dithiobis-, Morpholine, 4,4'-dithiodi-, Morpholine, N,N'-disulfide-, Morpholino disulfide, Morpholinodisulfide, N,N'-Bismorpholine disulfide, N,N-Dithiodimorpholine, Sanfel R, Sulfasan, Sulfasan R, Vanax A, Vulnoc, DTDM, Morpholine disulfide, 4,4'-Dithiodimorpholin, SULFASAN(R) R, Morpholine N,N'-disulfide, N,N'-DIMORPHOLINE DISULFIDE, N,N'-DITHIOBIS(MORPHOLINE), VANAX A, VANAX A FINE GRIND, VANAX A RODFORM, 4,4'-DITHIODIMORPHOLINE,



4,4'-dithiodimorpholine (DTDM) is white or light yellow crystal (or powder).
4,4'-dithiodimorpholine (DTDM) is white or yellowish needle-like crystal.
4,4'-dithiodimorpholine (DTDM) is a white crystalline or powder.


Specific gravity of 4,4'-dithiodimorpholine (DTDM) is 1.28-1.32.
4,4'-dithiodimorpholine (DTDM) has no poison.
4,4'-dithiodimorpholine (DTDM) is soluble in benzene, alcohol and acetone.


4,4'-dithiodimorpholine (DTDM) is insoluble in water.
The vulcanizing agent 4,4'-dithiodimorpholine (DTDM) can adapt to the vulcanization temperature of 140 °C-200 °C, and the scorch safety is good.
After reaching the normal vulcanization temperature, the vulcanization rate is accelerated, and the vulcanization property is ideal.


4,4'-dithiodimorpholine (DTDM) does not spray, does not pollute, and is easy to disperse in the rubber compound, and has good processing performance.
4,4'-dithiodimorpholine (DTDM) releases high-efficiency vulcanization rubber with high-efficiency vulcanization properties, which can significantly improve the resistance of vulcanizates.


4,4'-dithiodimorpholine (DTDM) can decompose morpholine free radicals with amine antioxidants in the rubber compound, which can make the vulcanized rubber have excellent heat and oxidation resistance.
4,4'-dithiodimorpholine (DTDM) has excellent thermal properties and is ideal for the manufacture of dynamic heat-resistant rubber products.


With the increase of people's environmental protection concepts and health concerns, it has been found that the vulcanizing agents 4,4'-dithiodimorpholine (DTDM) and thiuram products will cleave at the vulcanization temperature to release secondary amino-based molecular fragments, which can be combined with the nitroso donor to produce carcinogens.


4,4'-dithiodimorpholine (DTDM) can reduce the heat-generating NR and SNR and is an ideal rubber vulcanizing agent.
Nitrosamines, so the production and application of vulcanizing agents 4,4'-dithiodimorpholine (DTDM) and thiurams are subject to the limits and warnings of European and American countries and environmental regulations.


At present, the new vulcanizing agent DTDC (N, N-di(ε-caprolactam) disulfide) has attracted international attention due to the fact that it does not produce nitrosamines during vulcanization.
It is considered to be a vulcanizing agent 4,4'-dithiodimorpholine (DTDM) and disulfide or hexasulfurate.


The best alternative to M, replacing the vulcanizing agent 4,4'-dithiodimorpholine (DTDM) with the same amount, without changing the formulation and process of the compound.
4,4'-dithiodimorpholine (DTDM) molecule contains a total of 30 atom(s).


There are 16 Hydrogen atom(s), 8 Carbon atom(s), 2 Nitrogen atom(s), 2 Oxygen atom(s), and 2 Sulfur atom(s).
A chemical formula of 4,4'-dithiodimorpholine (DTDM) can therefore be written as: C8H16N2O2S2
The chemical formula of 4,4'-dithiodimorpholine (DTDM) shown above is based on the molecular formula indicating the numbers of each type of atom in a molecule without structural information, which is different from the empirical formula which provides the numerical proportions of atoms of each type.


The chemical formula of 4,4'-dithiodimorpholine (DTDM) is the basis of stoichiometry in chemical equations, i.e., the calculation of relative quantities of reactants and products in chemical reactions.
The law of conservation of mass dictates that the quantity of each element given in the chemical formula of 4,4'-dithiodimorpholine (DTDM) does not change in a chemical reaction.


Thus, each side of the chemical equation must represent the same quantity of any particular element based on the chemical formula of 4,4'-dithiodimorpholine (DTDM).
4,4'-dithiodimorpholine (DTDM) is the offering body of the sulphur.


4,4'-dithiodimorpholine (DTDM) will release a percentage of 27 active sulphur in the temperature of vulcanization.
4,4'-dithiodimorpholine (DTDM) will produce a high connecting effect to the rubber, part or whole replace the sulphur, so make the active sulphur gain an ideal physical machine function.


That makes up half effective structure rubber tesist not only fatigue but also oxidation.
According to 4,4'-dithiodimorpholine (DTDM)’s special chemical structure in the performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.


4,4'-dithiodimorpholine (DTDM) is non flammable.
4,4'-dithiodimorpholine (DTDM), synonymous with DTDM and Vulcanizing Agent DTDM, is a sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure systems.


4,4'-dithiodimorpholine (DTDM) is a white crystline powder or granule that is primarily used in the production of synthetic rubbers and adhesives.
4,4'-dithiodimorpholine (DTDM) 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.


4,4'-dithiodimorpholine (DTDM), synonymous with DTDM and Vulcanizing Agent DTDM, is a sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure systems.
4,4'-dithiodimorpholine (DTDM) is a white crystline powder or granule that is primarily used in the production of synthetic rubbers and adhesives.


4,4'-dithiodimorpholine (DTDM) is a vulcanizing agent and promoter of natural and synthetic rubber, it can release the sulphur in the vulcanizing temperature.
4,4'-dithiodimorpholine (DTDM) is a white or similar white crystal


4,4'-Dithiodimorpholine (DTDM) is an organic compound that has been used in a variety of scientific research applications.
4,4'-dithiodimorpholine (DTDM) is a white, solid, crystalline compound with a molecular weight of 256.35 g/mol.
4,4'-dithiodimorpholine (DTDM) is insoluble in water, but soluble in polar organic solvents.


4,4'-dithiodimorpholine (DTDM) is a versatile reagent and has been used in a variety of organic and inorganic syntheses.
4,4'-dithiodimorpholine (DTDM) is suitable for vulcanizing temperature between 140°C to 200°C.
4,4'-dithiodimorpholine (DTDM) has no blooming and pollution and is easy to disperse in sizing materials with good processability.


4,4'-dithiodimorpholine (DTDM) improves reducibility resistance of vulcanizing rubber.
4,4'-dithiodimorpholine (DTDM) exhibits excellent thermal and anti-oxidative performance to produce dynamic heat resistance in rubber products.
4,4'-dithiodimorpholine (DTDM) helps to reduce heat build-up property in NR and SBR.
Store 4,4'-dithiodimorpholine (DTDM) in a cool and dry place with good ventilation.



USES and APPLICATIONS of 4,4'-DITHIODIMORPHOLINE (DTDM):
Generally, 4,4'-dithiodimorpholine (DTDM) is used in combination, or sulfenamide or thiazole accelerator is used to adjust the scorch period and vulcanization rate.
4,4'-dithiodimorpholine (DTDM) can be used as a vulcanizing agent and accelerator for natural rubber and synthetic rubber.


4,4'-dithiodimorpholine (DTDM) is mainly used as vulcanization agent and accelerator for natural rubber and artificial rubber.
Under vulcanizing temperature, 4,4'-dithiodimorpholine (DTDM) can decompose active sulfur, whose content is 27%.
4,4'-dithiodimorpholine (DTDM) is primarily used in the synthesis of organosulfur compounds and has also been used in the synthesis of other organic and inorganic compounds such as nitriles, amides, and heterocycles.


In cross linking reaction, 4,4'-dithiodimorpholine (DTDM) mainly forms mono-sulfur bond.
4,4'-dithiodimorpholine (DTDM) is used in formulation or re-packing and at industrial sites.
4,4'-dithiodimorpholine (DTDM) is used in the following products: polymers.


Release to the environment of 4,4'-dithiodimorpholine (DTDM) can occur from industrial use: formulation of mixtures and formulation in materials.
4,4'-dithiodimorpholine (DTDM) is used for the manufacture of: rubber products.
Release to the environment of 4,4'-dithiodimorpholine (DTDM) can occur from industrial use: as processing aid.


Application of 4,4'-dithiodimorpholine (DTDM): Sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure system; provide heat/reversion/aging resistance in NR and synthetic rubbers; non-blooming; excellent storage safety.
4,4'-dithiodimorpholine (DTDM) is used sulphur donor vulcanizing agent for efficient vulcanization and semi-efficient vulcanization cure system; provide heat/reversion/aging resistance in NR and synthetic rubbers; non-blooming; excellent storage safety.


4,4'-dithiodimorpholine (DTDM) can be used to improve the anti-retrogradation and anti-thermal aging properties of sulfur vulcanized elastomer.
4,4'-dithiodimorpholine (DTDM) can be used as vulcanizing agent and accelerator for natural rubber and synthetic rubber.
The rubber feed of this product does not spray frost, pollution, discoloration and easy dispersion.


The vulcanizates obtained when used in effective and half-effect vulcanization systems have good heat resistance and aging resistance.
Active sulfur can be released at vulcanization temperature, the effective sulfur content is 27%, the operation is safe, the vulcanization speed is slow when used alone, and the use of thiazole, thiuram and dithiocarbamate can increase the vulcanization speed.


4,4'-dithiodimorpholine (DTDM) is especially suitable for butyl rubber.
4,4'-dithiodimorpholine (DTDM) is produced in the manufacture of tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products.
4,4'-dithiodimorpholine (DTDM) is also used as an asphalt stabilizer for vertical highways.


4,4'-dithiodimorpholine (DTDM) is suitable for natural rubber and synthetic rubber, with the characteristics of heat resistance, fatigue resistance, reduction resistance, no frost spraying, and scorch prevention.
4,4'-dithiodimorpholine (DTDM) can be used in the butyl rubber to produce tyre, butyl inner tube of tire, rubber belt and anti-heat rubber products, it also can be used as pitch stabilizer in the expressway.


4,4'-dithiodimorpholine (DTDM) is widely used in articles resistant to reversion based on NR such as tyre carcasses & ageing resistant articles based on SBR, NBR and EPDM
4,4'-dithiodimorpholine (DTDM) can be used as vulcanizing agent and accelerator of natural rubber and synthetic rubber.


4,4'-dithiodimorpholine (DTDM) does not spray frost, does not pollute, does not change color, easy to disperse.
The vulcanized rubber has good heat resistance and aging resistance when used in effective and semi-effective vulcanization systems.
At the sulfurization temperature can release the active sulfur, effective sulfur content is 27%, safe operation, when 4,4'-dithiodimorpholine (DTDM) is used alone the sulfurization speed is slow, and thiazole class, thiuram class and dithiocarbamate can be used to increase the sulfurization speed.


4,4'-dithiodimorpholine (DTDM) is especially suitable for butyl rubber, mainly used in the manufacture of tire, butyl inner tube, rubber belt and heat resistant rubber products, also used in highway asphalt stabilizer.
4,4'-dithiodimorpholine (DTDM) is used suitable for natural rubber and synthetic rubber, with heat resistance, fatigue resistance, anti-reduction, no frost, anti-scorch characteristics


4,4'-dithiodimorpholine (DTDM) acts as a vulcanizing agent.
Recommended of 4,4'-dithiodimorpholine (DTDM) to be used in rubber.
4,4'-dithiodimorpholine (DTDM) is produced in the manufacture of tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products.



APPLICATION AND CHARACTERISTICS OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is mainly used as vulcanized agent and accelerator for natural rubber and artificial rubber.
Under vulcanizing temperature, 4,4'-dithiodimorpholine (DTDM) can decompose active sulfur, whose content is 27%.
In cross linking reaction, 4,4'-dithiodimorpholine (DTDM) mainly forms monosulphur bond. Its usual use level is 0.5-2 orders.
4,4'-dithiodimorpholine (DTDM), which has the characteristic of processing safely, is usually used together with such accelerators as thiazoles, thiuram, dithiocarbamates etc.



FEATURES OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is the offering body of the sulphur.
4,4'-dithiodimorpholine (DTDM) will release a percentage of 27 active sulphur in the temperature of vulcanization.
4,4'-dithiodimorpholine (DTDM) will produce a high connecting effect to the rubber, part or whole replace the sulphur, so make the active sulphur gain an ideal physical machine function.

That makes up half effective structure rubber tesist not only fatigue but also oxidation.
According to 4,4'-dithiodimorpholine (DTDM)’s special chemical structure in the performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.

So many rubber products manufacturers including domestic and overseas pay attention to 4,4'-dithiodimorpholine (DTDM).
Vulcanization temperature, in addition to release active sulphur, so that make the rubber produce a high connecting function, morphlinyl, which has the second amine structure feature.

This kind of free radical can not only resist heat and oxygen, but also delay coking time, so that speed up vulcanization.
So, 4,4'-dithiodimorpholine (DTDM)has a performance of vulcanized agent ,promoter, anti- oxidantand prevent coking comprehensive effect.
So many rubber products manufacturers including domestic and overseas pay attention to 4,4'-dithiodimorpholine (DTDM).



CHARACTER OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is a white needle-like crystal.
Relative density 1.32-1.38.
4,4'-dithiodimorpholine (DTDM) is soluble in benzene, carbon tetrachloride, slightly soluble in acetone, gasoline, insoluble in ethanol, ether, insoluble in water.
4,4'-dithiodimorpholine (DTDM) is decomposition in the presence of an inorganic acid or base.
4,4'-dithiodimorpholine (DTDM) is stable storage at room temperature. 4,4'-dithiodimorpholine (DTDM) is non-toxic, fishy.



WHAT IS 4,4'-DITHIODIMORPHOLINE (DTDM) AND WHERE IS 4,4'-DITHIODIMORPHOLINE (DTDM) FOUND?
4,4'-dithiodimorpholine (DTDM) is used as an accelerator and vulcanizing agent used in rubber products.
4,4'-dithiodimorpholine (DTDM) is also used to protect metals against corrosion and tarnish by acid fumes as well as in toiletry and cosmetic products, hair conditioners, deodorant products and hair dyes.
4,4'-dithiodimorpholine (DTDM) is also found in pharmaceuticals for local anesthetics and antibiotics.
Further research may identify additional product or industrial usages of 4,4'-dithiodimorpholine (DTDM).



PRODUCTION METHOD OF 4,4'-DITHIODIMORPHOLINE (DTDM):
add morpholine, solvent gasoline (or benzene and toluene) and a small amount of water to the reaction kettle.
After stirring evenly, add sulfur monochloride, gasoline and sodium hydroxide solution dropwise into the kettle at the same time, control the temperature below 10 ℃, and add the sodium hydroxide solution slightly before a carbon chloride dropwise.

After dropping, add a certain amount of water and continue stirring for 30min.
The reactants are then pumped out, and the filtrate is separated from the water phase of gasoline and recovered.
The filter cake is added to the centrifuge and washed with water to be neutral.
After removing the water, 4,4'-dithiodimorpholine (DTDM) is dried to obtain the finished product.



SOURCES/USES OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is used as a stain protector for rubber, a vulcanizer (sulfur donor) and accelerator for natural and synthetic rubbers, a fungicide, and a curing agent for poly(fluoroalkoxyphosphazenes).



CHARACTERISTICS AND APPLICATION OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is mainly used as vulcanized agent and accelerator for natural rubber and artificial rubber.
Under vulcanizing temperature, 4,4'-dithiodimorpholine (DTDM) can decompose active sulfur, whose content is 27%.
In cross linking reaction, 4,4'-dithiodimorpholine (DTDM) mainly forms monosulphur bond.

4,4'-dithiodimorpholine (DTDM)s usual use level is 0.5-2 orders.
4,4'-dithiodimorpholine (DTDM), which has the characteristic of processing safely, is usually used together with such accelerators as thiazoles, thiuram, dithiocarbamates etc.



SCIENTIFIC RESEARCH APPLICATIONS OF 4,4'-DITHIODIMORPHOLINE (DTDM):
Chemical Synthesis and Organic Chemistry: 4,4'-dithiodimorpholine (DTDM)'s used in the synthesis of thiiranes, contributing to the study of organic chemical reactions.

*Toxicology: Research has shown that 4,4'-dithiodimorpholine (DTDM) exhibits significant embryotoxicity, making it a critical subject in studies related to chemical toxicity and environmental safety.

*Medical Applications: 4,4'-dithiodimorpholine (DTDM) has potential as a lead compound in treating neoplastic lesions of the cervix by acting on the oncoprotein E6 of human papillomavirus-16.

*Antiviral Research: Studies have compared 4,4'-dithiodimorpholine (DTDM)'s effects with other compounds in treating HPV-related lesions, contributing to the development of antiviral therapies.

*Material Science and Engineering: 4,4'-dithiodimorpholine (DTDM)'s effects on the ageing properties of SBS-modified asphalts have been studied, indicating its role in improving the durability of road materials.

*Rubber Chemistry: Research has been conducted on 4,4'-dithiodimorpholine (DTDM)'effects on the mechanical properties of EPDM vulcanizate, an important aspect in the field of polymer science and rubber technology.



PURIFICATION METHODS OF 4,4'-DITHIODIMORPHOLINE (DTDM):
Crystallise 4,4'-dithiodimorpholine (DTDM) from hot aqueous dimethylformamide or EtOH.
4,4'-dithiodimorpholine (DTDM) is a fungicide.



MARKET OVERVIEW OF AND REPORT COVERAGE OF 4,4'-DITHIODIMORPHOLINE (DTDM):
4,4'-dithiodimorpholine (DTDM) is a chemical compound used as a crosslinking agent in the rubber industry.
4,4'-dithiodimorpholine (DTDM) is primarily used in the production of rubber products to improve their mechanical properties, such as hardness, flexibility, and abrasion resistance.

4,4'-dithiodimorpholine (DTDM) is widely used in the manufacturing of rubber tires, seals, gaskets, conveyor belts, and other rubber products.
The future outlook of the 4,4'-dithiodimorpholine (DTDM) market is promising.
The increasing demand for rubber products across various industries such as automotive, construction, and electronics is driving the growth of this market.

The rising focus on improving the performance and durability of rubber products to meet the stringent quality standards is further boosting the demand for 4,4'-dithiodimorpholine (DTDM).
Moreover, the growing automotive industry, particularly in emerging economies, is expected to fuel the demand for rubber tires, which, in turn, will drive the demand for 4,4'-dithiodimorpholine (DTDM).

Additionally, the increasing environmental concerns and regulations regarding the disposal of rubber waste are encouraging manufacturers to seek sustainable and eco-friendly rubber products, further driving the market growth.
The current outlook of the 4,4'-dithiodimorpholine (DTDM) market is positive, with steady growth observed in recent years.

The market is characterized by the presence of several key players who are actively engaged in research and development activities to enhance product performance and expand their market share.
Manufacturers are also focusing on strategic partnerships, collaborations, and acquisitions to strengthen their market position and gain a competitive edge.

Overall, the 4,4'-dithiodimorpholine (DTDM) market is expected to witness significant growth in the coming years.
With increased demand for high-quality and durable rubber products, coupled with technological advancements in the manufacturing process, the market is projected to grow at a CAGR of % during the forecasted period.



PHYSICAL and CHEMICAL PROPERTIES of 4,4'-DITHIODIMORPHOLINE (DTDM):
Molecular Weight:236.35500
Exact Mass:236.35
EC Number:203-103-0
UNII:M786P489YF
NSC Number:65239
DSSTox ID:DTXSID8026698
Color/Form:CRYSTALS|GRAY TO TAN POWDER
PSA:75.54000
XLogP3:0.73800
Appearance:DryPowder; DryPowder, PelletsLargeCrystals; PelletsLargeCrystals
Density:1.36 g/cm3 @ Temp: 25 °C
Melting Point:125 °C
Boiling Point:371.7ºC at 760 mmHg
Flash Point:154ºC
Refractive Index:1.6300 (estimate)

Storage Conditions: Refrigerator
Melting Point: 124-125°C
Boiling Point: 371.7±52.0 °C at 760 mmHg
Flash Point: 178.6±30.7 °C
Molecular Formula: C8H16N2O2S2
Molecular Weight: 236.355
Density: 1.3±0.1 g/cm3
CAS: 103-34-4
EINECS: 203-103-0
InChI: InChI=1/2C4H9NO.2S/c2*1-3-6-4-2-5-1;;/h2*5H,1-4H2;;/q;;2*-2
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
Molecular Formula: C8H16N2O2S2
Molar Mass: 236.35
Density: 1.32~1.38g/cm3

Melting Point: 124-125°C
Boling Point: 371.7±52.0 °C(Predicted)
Water Solubility: 215mg/L at 20.2℃
Vapor Presure: 0.004Pa at 25℃
Appearance: White powder
Specific Gravity: 1.36
Color: White to Almost white
Merck: 14,3372
pKa: 0.78±0.20(Predicted)
Storage Condition: Refrigerator
Refractive Index: 1.6300 (estimate)
MDL: MFCD00023319
Physical and Chemical Properties: White needle-like crystals.
Fish Odor.

Molecular Weight: 236.4 g/mol
XLogP3-AA: 0.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 3
Exact Mass: 236.06532010 g/mol
Monoisotopic Mass: 236.06532010 g/mol
Topological Polar Surface Area: 75.5Ų
Heavy Atom Count: 14
Formal Charge: 0
Complexity: 143
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: 103-34-4
Formula: C8H16N2O2S2
Molecular weight: 236,35 g/mol
Melting point: 124-125°C
Boiling point: 371.7±52.0 °C(Predicted)
Density: 1.32~1.38g/cm3
vapor pressure: 0.004Pa at 25℃
refractive index: 1.6300 (estimate)
storage temp.: Refrigerator
form: powder to crystaline
pka: 0.78±0.20(Predicted)
color: White to Almost white
Specific Gravity: 1.36
Water Solubility: 215mg/L at 20.2℃

Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
LogP: 2.67 at 22℃
Indirect Additives used in Food Contact Substances: 4,4'-DITHIODIMORPHOLINE
FDA 21 CFR: 175.105; 177.2600
CAS DataBase Reference: 103-34-4(CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: M786P489YF
NIST Chemistry Reference: Morpholine disulfide(103-34-4)
EPA Substance Registry System: Morpholine, 4,4'-dithiobis- (103-34-4)
Melting point : 124-125°C
Boiling point : 371.7±52.0 °C(Predicted)
density : 1.32~1.38g/cm3
vapor pressure: 0.004Pa at 25℃
refractive index :1.6300 (estimate)
storage temp. : Refrigerator

form : powder to crystaline
pka: 0.78±0.20(Predicted)
color: White to Almost white
Specific Gravity: 1.36
Water Solubility: 215mg/L at 20.2℃
Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
LogP: 2.67 at 22℃
CAS DataBase Reference: 103-34-4(CAS DataBase Reference)
NIST Chemistry Reference: Morpholine disulfide(103-34-4)
EPA Substance Registry System: Morpholine, 4,4'-dithiobis- (103-34-4)
Physical state: powder
Color: white
Odor: No data available

Melting point/freezing point:
Melting point/range: 125,0 °C - OECD Test Guideline 102
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: No data available
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: 0,215 g/l at 20,2 °C
Partition coefficient:
n-octanol/water:
log Pow: 2,67 at 22 °C

Vapor pressure: 0,00004 hPa at 25 °C
Density: 0,4525 g/cm3 at 20 °C
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: No data available
Molecular Formula / Molecular Weight: C8H16N2O2S2 = 236.35
Physical State (20 deg.C): Solid
Storage Temperature: 0-10°C
Condition to Avoid: Heat Sensitive
CAS RN 103-34-4
Reaxys Registry Number: 126214

PubChem Substance ID: 87566980
SDBS (AIST Spectral DB): 10257
Merck Index (14): 3372
MDL Number: MFCD00023319
CAS: 103-34-4
Color: White-Yellow
MDL Number: MFCD00023319
Synonym: N,N′C-Dimorpholine Disulfide, N,N′C-Dithiobis(morpholine)
SMILES: C1COCCN1SSN2CCOCC2
Molecular Weight (g/mol): 236.348
Formula Weight: 236.35
Physical Form: Crystalline Powder
Melting Point: 125°C
Molecular Formula: C8H16N2O2S2
InChI Key: HLBZWYXLQJQBKU-UHFFFAOYSA-N
IUPAC Name: 4-(morpholin-4-yldisulfanyl)morpholine

PubChem CID: 7648
Percent Purity: ≥98.0% (HPLC,N)
Chemical Name or Material: 4,4′-Dithiodimorpholine
CAS No.: 103-34-4
Molecular Formula: C8H16N2O2S2
InChIKeys: InChIKey=HLBZWYXLQJQBKU-UHFFFAOYSA-N
Molecular Weight: 236.35500
Exact Mass: 236.35
EC Number: 203-103-0
UNII: M786P489YF
NSC Number: 65239
DSSTox ID: DTXSID8026698
Color/Form: CRYSTALS|GRAY TO TAN POWDER
Categories: Antioxidants
PSA: 75.54000
XLogP3: 0.73800
Appearance: DryPowder; DryPowder, PelletsLargeCrystals; PelletsLargeCrystals

Density: 1.36 g/cm3 @ Temp: 25 °C
Melting Point: 125 °C
Boiling Point: 371.7ºC at 760 mmHg
Flash Point: 154ºC
Refractive Index: 1.6300 (estimate)
Storage Conditions: Refrigerator
Density: 1.36
Appearance: White Crystal powder
Melting Point: 120 degC min
Ash: 0.30% max
Particle Size: Max- 1.0(63um), 0.50(um)
Oil: 0; 1.0~2.0
Loss on Drying: 0.30% max
Specific gravity: 1.28~1.32

Molecular weight: 236.38
Melting point : 124-125°C
Boiling point : 371.7±52.0 °C(Predicted)
density: 1.32~1.38g/cm3
vapor pressure : 0.004Pa at 25℃
refractive index: 1.6300 (estimate)
storage temp.: Refrigerator
pka: 0.78±0.20(Predicted)
form: powder to crystaline
color: White to Almost white
Specific Gravity: 1.36
Water Solubility: 215mg/L at 20.2℃
Merck: 14,3372
InChIKey: HLBZWYXLQJQBKU-UHFFFAOYSA-N
LogP: 2.67 at 22℃



FIRST AID MEASURES of 4,4'-DITHIODIMORPHOLINE (DTDM):
-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.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
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 4,4'-DITHIODIMORPHOLINE (DTDM):
-Personal precautions, protective equipment and emergency procedures:
*Advice for non-emergency personnel:
Ensure adequate ventilation.
-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 4,4'-DITHIODIMORPHOLINE (DTDM):
-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:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of 4,4'-DITHIODIMORPHOLINE (DTDM):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face 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
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of 4,4'-DITHIODIMORPHOLINE (DTDM):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of 4,4'-DITHIODIMORPHOLINE (DTDM):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available

4-ETHYLOCT-1-YN-3-OL
4-ethyloct-1-yn-3-ol's an alcohol with a triple bond (alkyne) located at the first carbon of an eight-carbon chain, with an ethyl group (C2H5) attached to the fourth carbon.
4-ethyloct-1-yn-3-ol is a chemical compound that belongs to the family of alkynes.
4-ethyloct-1-yn-3-ol is a colorless liquid with a strong odor and is commonly used in the fragrance industry.

CAS Number: 5877-42-9
Molecular Formula: C10H18O
Molecular Weight: 154.25
EINECS Number: 227-545-9

4-Ethyl-1-octyn-3-ol, 4-Ethyloct-1-yn-3-ol, 5877-42-9, 1-Octyn-3-ol, 4-ethyl-, Ethyloctynol, 4-Ethyl-1-octyn-3-0l, 4-Ethyl-3-hydroxy-1-octyne, (2-Ethyl-1-hydroxyhexyl)acetylene, L1LYK1CE9P, DTXSID1044697, MFCD00015262, NSC-62119, EINECS 227-545-9, UNII-L1LYK1CE9P, NSC 62119, 1-Octyne-3-ol, 4-ethyl-, NSC62119, SCHEMBL179938, DTXCID9024697, Tox21_301468, AKOS006229979, NCGC00256162-01, SY053582, CAS-5877-42-9, CS-0077154, E0270, NS00022432, A869369, Q27282598, InChI=1/C10H18O/c1-4-7-8-9(5-2)10(11)6-3/h3,9-11H,4-5,7-8H2,1-2H

4-ethyloct-1-yn-3-ol is a chemical compound.
The systematic name follows the IUPAC nomenclature rules for organic chemistry, where the numbering of the carbon chain starts from the end nearest to the functional group, which in this case is the alcohol (-OH) group.
However, recent studies have shown that 4-ethyloct-1-yn-3-ol has potential therapeutic and environmental applications.

There total 3 articles about 4-ethyloct-1-yn-3-ol which guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology.
4-ethyloct-1-yn-3-ol uses and applications include: Corrosion inhibitor in oil well acidizing, mild steel pickling, mild steel cleaning in acid systems; electroplating bath additive; curative for paints, elastomers, adhesives

So, it's called 4-ethyloct-1-yn-3-ol because the triple bond (alkyne) is at the first carbon, the ethyl group is attached to the fourth carbon, and the hydroxyl (alcohol) group is on the third carbon of the octane chain.
They are insoluble in water but easily soluble in common organic solvents of low polarity.
The characteristics of alkynes in chemical synthesis are due to the acidity of hydrogen atoms bonded to triple bonded carbons as well as to the triple bonds themselves.

Addition reactions are typical of alkyne reactions; halogenation, hydrogenation, hydrohalogenation, hydration, oxidative cleavage, nitrile formation and acidity of terminal alkynes.
Polymerization and substitution reactions are also useful in chemical synthesis.
Catalytic hydrogenation by Pt and Pd hydrogenation catalysts to produce alkanes without isolation of alkene intermediates.

Catalytic hydrogenation by Lindlar catalyst to produce cis- or trans-alkenes without further reduction to alkanes Addition by electrophilic reagents.
Addition of halides (chlorine, bromine, iodine) to produce dihalogenated alkanes substituted at the solid binding site.
Addition of hydrogen halides (HCl, HBr, HI) to produce monohalogen substituted alkenes or dihalogen substituted alkanes.

Hydration of alkynes to give ketone products by the enol tautomeric intermediate step, while hydration of solid bonds gives alcoholic products (exceptionally acetylene gives acetaldehyde).
Hydroboration with disiamylborane to give ketones or aldehydes.
Oxidative cleavages of the triple bond to give carboxylic acid products with oxidizing agents (potassium permanganate and ozone).

Nucleophilic addition by sp hybrid carbon atoms of the alkyne triple bond (nitrile formation).
Nucleophilic reduction by sodium solutions in liquid ammonia to trans-alkenes.
The name of all 4-ethyloct-1-yn-3-ol ends with "-yne" by adding a prefix to indicate the location of the triple bond in the molecule.

Previously known compositions for inhibiting corrosion of aluminum surfaces when contacted with aqueous acids have been used with varying degrees of success.
A shortcoming of these prior art corrosion inhibiting compositions is that they cease to be effective after relatively short periods of time or decompose under elevated temperature conditions, i.e. temperatures in the range. range of 125 ° to 175 ° F, or more.
Another shortcoming of these prior art compositions is that they are not effective to a comparable degree for virtually all commonly used aluminum alloys.

The present invention relates to novel and useful compositions which can be used in acidic solutions to decrease or inhibit corrosion of aluminum in contact with acidic solutions.
The present invention provides a corrosion inhibitor for inhibiting corrosion of aluminum and its alloys by aqueous acids, which inhibitor comprises an anionic surfactant and an acetylenic compound.
The invention further provides a method for inhibiting corrosion of aluminum and its alloys.

The present invention is particularly useful for cleaning aluminum with aqueous acids, such as removing scale from heat exchangers, tanks, pipes, etc. aluminum, with chlorh acid diluted and to inhibit corrosion of tanks, pipes, etc. aluminum, which must contain dilute acids.
4-ethyloct-1-yn-3-ol composition and method of inhibiting corrosion of aluminum surfaces when such surfaces are contacted with aqueous acids.
Another object of the present invention is to provide an inhibitory composition and a method for inhibiting corrosion of aluminum surfaces when contacted with aqueous acids, which composition and method are effective both in low temperatures than high temperatures.

Another object of the present invention is to provide an inhibitor composition and a method for inhibiting the corrosion of aluminum and its alloys when contacted with acid solutions, in particular hydrochloric acid.
Yet another object of the present invention is to provide an inhibitor composition and a method of inhibiting aluminum and its alloys when contacted with acidic solutions whereby a comparable degree of inhibition of aluminum. Corrosion can be obtained for the most commonly used aluminum alloys.
These objects and advantages of the present invention, as well as others, will become readily apparent from the description of the invention and the examples which follow.

4-ethyloct-1-yn-3-ol consists of a chain of 10 carbon atoms (octane), with a triple bond between the first and second carbon atoms (1-yn), an ethyl group (C2H5) attached to the fourth carbon atom (4-ethyl), and a hydroxyl group (-OH) attached to the third carbon atom (3-ol).
4-ethyloct-1-yn-3-ol contains both an alkyne (triple bond) and an alcohol (hydroxyl) functional group.
Physical Properties: As an alcohol, 4-ethyloct-1-yn-3-ol is likely to be a colorless liquid at room temperature.

4-ethyloct-1-yn-3-ol can be synthesized through various methods, including alkyne hydroxylation reactions or alkyne reduction followed by oxidation to introduce the hydroxyl group.
4-ethyloct-1-yn-3-ols like this can have applications in organic synthesis, as intermediates in the production of pharmaceuticals, or in research settings for studying chemical reactions involving alkynes and alcohols.

Melting point: 1.9°C (estimate)
Boiling point: 130°C 59mm
Density: 0,873 g/cm3
refractive index: 1.448-1.453
pka: 13.09±0.20(Predicted)
form: clear liquid
color: Colorless to Light yellow to Light orange

Depending on the synthesis method and reaction conditions, 4-Ethyloct-1-yn-3-ol may exist as a mixture of stereoisomers or exhibit stereochemistry due to the presence of chiral centers.
Resolution of stereoisomers may be necessary for certain applications, particularly in pharmaceutical synthesis where enantiopurity is crucial.
The presence of both an alkyne and an alcohol group in 4-Ethyloct-1-yn-3-ol allows for various functional group interconversions.

For example, the alkyne group can be converted to a variety of other functional groups such as alkenes, ketones, or carboxylic acids through appropriate chemical reactions.
4-ethyloct-1-yn-3-ols containing alkynes and alcohol functional groups can exhibit diverse biological activities.
Therefore, 4-Ethyloct-1-yn-3-ol or its derivatives may have potential pharmacological properties that could be explored through biological assays and testing, such as antimicrobial, anticancer, or enzyme inhibitory activities.

Various analytical techniques can be employed to characterize and identify 4-Ethyloct-1-yn-3-ol, including spectroscopic methods such as nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectrometry (MS).
These techniques provide valuable information about the molecular structure, functional groups, and purity of the compound.
4-ethyloct-1-yn-3-ol should be stored in a cool, dry place away from direct sunlight and sources of heat.

4-ethyloct-1-yn-3-ol should also be protected from moisture and air to prevent degradation or unwanted chemical reactions.
Proper storage conditions ensure the stability and longevity of the compound for future use.
Based on a volume of 100%, a preferred composition of the present invention is composed as follows: Percent of anionic surface active agent 15-35 acetylene compound 65-85.

Another preferred composition of the present invention consists of the following: Percent - Anionic surfactant 15-35 Acetylenic compound 30-60 Nitrogenous compound 0-8 Non-acetylenic alcohol 10-50.
Yet another preferred composition of the present invention consists of the following: Percent anionic surface active agent 15-35 Acetylenic compound 30-60 Nitrogenous compound 0-8 Aldehyde 10-30 Non-acetylenic
alcohol 5-15.
The non-acetylenic alcohol not only acts as a diluent and / or solubilizer, but also contributes to the corrosion inhibiting efficiency of the new composition for certain applications.

The nitrogen compound also contributes to the corrosion inhibiting efficiency of the new composition for some aluminum alloys, as does aldehyde.
Based on 100% volume, a more specific preferred composition, sometimes referred to herein as composition A, of the present invention is as follows:
Composition A Compound Parts in percentage volume by volume CRA 1.0 30.0 Ethyl octinol 2.33 70.0.

Another preferred specific composition, sometimes referred to herein as composition B, is as follows: Composition B Parts of the compound in percentage volume by volume CRA 1.0 30.0 Ethyl octinol 1.6 49.0 Diacetone Alcohol 0.7 21.0
4-ethyloct-1-yn-3-ol is a terminal alkyne, meaning it has the triple bond at the end of the carbon chain.
This makes 4-ethyloct-1-yn-3-ol more reactive than internal alkynes.

The presence of the hydroxyl group (alcohol) also adds to its reactivity, allowing it to participate in various chemical reactions such as nucleophilic substitution, acid-base reactions, and oxidation.
One method for synthesizing 4-ethyloct-1-yn-3-ol involves starting with an octyne compound and performing an addition reaction with ethylmagnesium bromide (Grignard reagent), followed by acidic workup to introduce the alcohol group.
Alternatively, 4-ethyloct-1-yn-3-ol can be prepared by alkyne hydroxylation reactions using appropriate reagents under specific conditions.

The triple bond in alkynes can undergo various reactions such as addition reactions, where other atoms or groups add to the carbon-carbon triple bond, forming new bonds.
The hydroxyl group can undergo typical alcohol reactions, including dehydration to form an alkyne or oxidation to form a carbonyl compound.
4-ethyloct-1-yn-3-ols containing terminal alkynes and alcohol groups have diverse applications.

They can be used in organic synthesis to construct complex molecules, as starting materials for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.
Additionally, they may serve as intermediates in the synthesis of natural products or as reagents in research laboratories.

As with handling any chemical compound, proper safety precautions should be taken.
This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following established protocols for handling, storage, and disposal.

Uses:
4-ethyloct-1-yn-3-ol can serve as a versatile building block in organic synthesis, allowing chemists to construct more complex molecules.
4-ethyloct-1-yn-3-ol is triple bond and alcohol functional group provide opportunities for diverse chemical transformations, enabling the synthesis of a wide range of compounds including pharmaceuticals, agrochemicals, and fine chemicals.
4-ethyloct-1-yn-3-ols containing terminal alkynes and alcohol groups have been investigated for their potential pharmaceutical properties.

They may serve as intermediates in the synthesis of biologically active molecules or as lead compounds in drug discovery efforts.
Biological activities such as antimicrobial, anticancer, and enzyme inhibitory effects could be explored.
4-ethyloct-1-yn-3-ol can be utilized as a reagent or substrate in chemical research laboratories to study various chemical reactions and mechanisms.

4-ethyloct-1-yn-3-ol is reactivity allows for the exploration of new synthetic routes and the development of novel chemical transformations.
4-ethyloct-1-yn-3-ol are important functional groups in materials science.
They can be incorporated into polymers, coatings, and other materials to modify their properties, such as adhesion, toughness, or conductivity.

4-ethyloct-1-yn-3-ol could potentially be used in the synthesis of specialty materials with tailored properties.
4-ethyloct-1-yn-3-ol is containing alkynes and alcohol groups may also find applications as catalysts in organic reactions.
They can participate in catalytic processes, facilitating the transformation of substrates into desired products with improved efficiency and selectivity.

4-ethyloct-1-yn-3-ol can be used as a reference standard or internal standard in analytical chemistry methods such as chromatography or spectroscopy.
4-ethyloct-1-yn-3-ol is known properties and behavior can aid in the identification and quantification of similar compounds in complex mixtures.
4-ethyloct-1-yn-3-ol is with terminal alkynes and alcohol groups may have applications in the development of agrochemicals such as herbicides, fungicides, and insecticides.

They could potentially serve as active ingredients or intermediates in the synthesis of these agricultural products, contributing to crop protection and pest management efforts.
The reactivity of alkynes and alcohols makes them suitable for modifying surfaces of various materials.
4-Ethyloct-1-yn-3-ol could be used to functionalize surfaces, enhancing properties such as adhesion, wettability, or biocompatibility.

This could find applications in coatings, adhesives, biomaterials, and other surface-sensitive technologies.
4-ethyloct-1-yn-3-ols have been investigated for their potential application in organic electronics, including organic photovoltaic (OPV) devices.
By incorporating 4-Ethyloct-1-yn-3-ol or its derivatives into organic semiconductors, researchers may explore its suitability for improving the efficiency and performance of OPV devices, contributing to renewable energy technologies.

4-ethyloct-1-yn-3-ols containing alkynes and alcohols have been studied for their potential use in chemical sensing applications.
Functionalizing sensor surfaces with molecules like 4-Ethyloct-1-yn-3-ol could enable the detection of specific analytes through selective chemical interactions, leading to the development of sensors for environmental monitoring, healthcare diagnostics, and industrial process control.
Terminal alkynes are commonly used in transition metal-catalyzed cross-coupling reactions, such as Sonogashira coupling and Glaser coupling.

4-Ethyloct-1-yn-3-ol could serve as a valuable substrate in these reactions, allowing for the synthesis of complex molecules with carbon-carbon bond formation under mild conditions.
Compounds with unique structural features, such as 4-Ethyloct-1-yn-3-ol, can be employed as chemical probes for investigating biological processes or molecular interactions.
By modifying the structure or functional groups of the 4-ethyloct-1-yn-3-ol, researchers can design probes tailored to specific targets, aiding in the study of biological systems and disease mechanisms.

Alkynes can be polymerized to form polyacetylenes, which have interesting electronic and mechanical properties.
4-Ethyloct-1-yn-3-ol could be polymerized to produce functionalized polyacetylenes, which may find applications in areas such as conductive polymers, organic electronics, and molecular electronics.
4-ethyloct-1-yn-3-ols containing alkynes are often used in bioconjugation reactions, where they can selectively react with azides via copper-catalyzed azide-alkyne cycloaddition (CuAAC) or strain-promoted azide-alkyne cycloaddition (SPAAC).

4-ethyloct-1-yn-3-ol could be incorporated into biomolecules or used as a linker for attaching various functional groups or labels in bioconjugation chemistry.
4-ethyloct-1-yn-3-ols and alcohols can be used as functional groups in the synthesis of metal-organic frameworks (MOFs), which are porous materials with potential applications in gas storage, separation, catalysis, and sensing.
4-Ethyloct-1-yn-3-ol could be incorporated into MOF structures to impart specific functionalities or enhance their properties for targeted applications.

By incorporating fluorescent dyes or labels onto 4-Ethyloct-1-yn-3-ol or its derivatives, it could be used as a fluorescent probe for imaging or sensing applications.
Fluorescently labeled compounds can be employed in fluorescence microscopy, flow cytometry, biosensing, and other fluorescence-based techniques for visualizing biological processes or detecting analytes with high sensitivity.
4-ethyloct-1-yn-3-ols containing terminal alkynes and alcohol groups are valuable intermediates in the synthesis of fine chemicals, which are high-value compounds used in various industries including pharmaceuticals, cosmetics, and specialty chemicals.

4-Ethyloct-1-yn-3-ol could be utilized in the synthesis of fragrance compounds, flavoring agents, or other specialty chemicals with specific functional groups or structural motifs.
4-ethyloct-1-yn-3-ol-containing compounds are used in bioorthogonal chemistry for labeling biomolecules, particularly proteins, through selective chemical reactions.
4-Ethyloct-1-yn-3-ol could be conjugated to proteins or peptides for site-specific labeling, imaging, or functionalization in biological research, diagnostics, or therapeutic applications.

Safety Profile:
4-Ethyloct-1-yn-3-ol is likely to be flammable.
4-ethyloct-1-yn-3-ol may form flammable vapors or gases when heated, which can ignite in the presence of a spark or flame.
Adequate precautions should be taken to prevent ignition sources and control fire hazards.

Inhalation of vapors or aerosols of 4-Ethyloct-1-yn-3-ol may cause irritation to the respiratory tract, including the nose, throat, and lungs.
Prolonged or repeated exposure to high concentrations may lead to respiratory irritation, coughing, or difficulty breathing.
4-ethyloct-1-yn-3-ol may cause irritation or dermatitis. Prolonged or repeated skin exposure may result in dryness, redness, itching, or chemical burns.

Skin contact should be avoided, and appropriate personal protective equipment, such as gloves and protective clothing, should be worn when handling the compound.
4-ethyloct-1-yn-3-ol may cause irritation or damage to the eyes. Symptoms of eye exposure may include redness, pain, tearing, and blurred vision.
Immediate flushing with water for at least 15 minutes is recommended in case of eye contact, and medical attention should be sought if irritation persists.


4-Hydroxyacetophenone
PROPYLPARABEN, N° CAS : 94-13-3 - 4-Hydroxybenzoate de propyle, Origine(s) : Synthétique. Autre langue : Propilparabeno. Nom INCI : PROPYLPARABEN. Nom chimique : Propyl 4-hydroxybenzoate. N° EINECS/ELINCS : 202-307-7. Additif alimentaire : E216. Noms français : Ester propylique de l'acide p-hydroxybenzoïque; N-PROPYL P-HYDROXYBENZOATE; P-HYDROXYBENZOIC ACID PROPYL ESTER; P-HYDROXYPROPYL BENZOATE; PROPYL 4-HYDROXYBENZOATE; PROPYL P-HYDROXY BENZOATE; PROPYL P-HYDROXYBENZOATE ; PROPYL PARABEN .Noms anglais : p-Hydroxybenzoic propyl ester; Utilisation et sources d'émission : Germicide, fabrication de cosmétiques
4-Hydroxybenzoate de propyle
4-Nitrobenzoic acid; PNBA 1-carboxy-4-nitrobenzene p-Nitrobenzoic acid; p-nitrobenzenecarboxylic acid 4-nitrodracylic acid Kyselina p-nitrobenzoova Acide 4-nitro benzoique CAS NO:62-23-7
4-METHOXYPHENOL
4-Methoxyphenol is a member of phenols and a member of methoxybenzenes.
4-Methoxyphenol has a role as a metabolite.
4-Methoxyphenol is a substrate of the enzyme tyrosinase and acts as a competitive inhibitor of melanogenesis.

CAS: 150-76-5
MF: C7H8O2
MW: 124.14
EINECS: 205-769-8

Synonyms
Eastman HQMME;ethermonomethyliqued’hydroquinone;Hqmme;Hydroquinone methyl ether;hydroquinonemethylether;Leucobasal;Leucodine b;leucodineb;4-Methoxyphenol;Mequinol;150-76-5;4-Hydroxyanisole;p-Hydroxyanisole;p-Methoxyphenol;Phenol, 4-methoxy-;HYDROQUINONE MONOMETHYL ETHER;Leucobasal;MEHQ;Leucodine B;Mechinolum;P-Guaiacol;Novo-Dermoquinona;Hydroquinone methyl ether;HQMME;p-Hydroxymethoxybenzene;para-methoxyphenol;1-Hydroxy-4-methoxybenzene;Monomethyl ether hydroquinone;PMF (antioxidant)
;Phenol, p-methoxy-;USAF AN-7;4-Methoxy-phenol;Mechinolo;Mequinolum;Mono methyl ether hydroquinone;NSC 4960;CCRIS 5531;BMS 181158;BMS-181158;DTXSID4020828;HSDB 4258;UNII-6HT8U7K3AM;NSC-4960;EINECS 205-769-8;6HT8U7K3AM;MFCD00002332;AI3-00841;NSC4960;DTXCID60828;SOLAGE COMPONENT MEQUINOL;CHEBI:69441;EC 205-769-8;Mequinol (INN);MEQUINOL COMPONENT OF SOLAGE;NCGC00091390-02;MEQUINOL [INN];MEQUINOL (MART.);MEQUINOL [MART.];Mechinolo [DCIT];Mequinolum [INN-Latin];CAS-150-76-5;Mequinol [USAN:INN:DCF];4methoxyphenol;paramethoxyphenol;p- methoxyphenol;p-methoxy phenol;p-methoxy-phenol;4-methoxy phenol;Eastman HQMME;para-hydroxyanisole;4-(methoxy)phenol;4HA;4KS;para- hydroxyanisole;4-(methyloxy)phenol;HQME;hydroquinone methylether;MEQUINOL [HSDB];MEQUINOL [USAN];Mequinol (USAN/INN);Mequinol, INN, USAN;MEQUINOL [VANDF];PHENOL,4-METHOXY;hydroxyquinone methyl ether;hydroquinone monomethylether;CHEMBL544;MEQUINOL [WHO-DD];NCIMech_000709

4-Methoxyphenol, MeHQ or 4-methoxyphenol, is an organic compound with the formula CH3OC6H4OH.
4-Methoxyphenol is a phenol with a methoxy group in the para position.
A colorless solid, 4-Methoxyphenol is used in dermatology and organic chemistry.

4-Methoxyphenol Chemical Properties
Melting point: 56 °C
Boiling point: 243 °C(lit.)
Density: 1,55 g/cm3
Vapor density: 4.3 (vs air)
Vapor pressure: Refractive index: 1.5286 (estimate)
Fp: >230 °F
Storage temp.: Store below +30°C.
Solubility: Soluble in acetone, ethyl acetate, ethanol, ether, benzene and carbon tetrachloride.
Form: Liquid
pka: 10.21(at 25℃)
Color: Clear colorless to pale yellow
Odor: at 1.00?%?in?dipropylene glycol. phenolic
PH: 5.1 (30g/l, H2O, 20℃)
Odor Threshold: 0.0027ppm
Water Solubility: 40 g/L (25 ºC)
BRN: 507924
Exposure limits ACGIH: TWA 5 mg/m3
NIOSH: TWA 5 mg/m3
Stability: Stable. Combustible. Incompatible with halogens, oxidizing agents.
InChIKey: NWVVVBRKAWDGAB-UHFFFAOYSA-N
LogP: 1.3 at 20℃
CAS DataBase Reference: 150-76-5(CAS DataBase Reference)
NIST Chemistry Reference: 4-Methoxyphenol (150-76-5)
EPA Substance Registry System: 4-Methoxyphenol (150-76-5)

4-Methoxyphenol is a colorless to white, waxy solid with an odor of caramel and phenol.
4-Methoxyphenol is a combustible solid.
4-Methoxyphenol is used as an inhibitor for acrylic monomers and as a stabilizer for chlorinated hydrocarbons, ethyl cellulose, and UV inhibitors.

Uses
4-Methoxyphenol is an active ingredient and used in dermatology.
4-Methoxyphenol is employed as a pharmaceutical drug in skin depigmentation.
4-Methoxyphenol is used as polymerization inhibitors.
For example, in the radical polymerization of acryaltes and styrene monomers.
4-Methoxyphenol is also used as an intermediate in the preparationagrochemicals, liquid crystals.
4-Methoxyphenol acts as a stabilizer for the formulation of inks, toners and adhesives.
4-Methoxyphenol is mainly used as an additive for textile and leather industries.

Organic chemistry
In organic chemistry 4-Methoxyphenol is used as a polymerisation inhibitor (e.g. acrylates or styrene monomers).
4-Methoxyphenol can be produced from p-benzoquinone and methanol via a free radical reaction.

Use in dermatology
4-Methoxyphenol is a common active ingredient in topical drugs used for skin depigmentation.
As a topical drug mequinol is often mixed with tretinoin, a topical retinoid.
A common formulation for this drug is an ethanolic solution of 2% mequinol and 0.01% tretinoin by mass.
Dermatologists commonly prescribe the drug to treat liver spots.
Lower dosages of mequinol have been used in conjunction with a Q-switched laser to depigment skin in patients with disseminated idiopathic vitiligo.

Synthesis
4-Methoxyphenol was synthesised according to Oxidation with H2O2 and a Diselenide catalyst.
p-Anisaldehyde (50 mmol) is dissolved in CH2Cl2 (100mL) and (o-NO2PhSe)2 (2 mmol) and 30% H2O2 (13mL, 128 mmol) are added.
The mixture is stirred magnetically at room temperature (water bath) for 30 minutes.
Insoluble catalyst is removed by filtration and washed with CH2Cl2 (20mL) and water (20mL).
4-Methoxyphenol can be reused after drying.
To the filtrate and washings, water (100mL) is added, and the layers are separated after shaking.
The organic layer is washed subsequently with 10% NaHSO3 (100mL), 10% Na2CO3 (100mL), water (100mL) and dried over Na2SO4.
4-Methoxyphenol is obtained by alkaline hydrolysis of the residue.
Yield: 93%.

Reactions
4-Methoxyphenol may be used in the synthesis of butylated hydroxy anisoles via alkylation with methyl tert-butyl ether over a non-zeolitic solid acidic catalyst.
This process is eco-friendly when compared to the Friedel-Crafts alkylation reaction.
4-Methoxyphenol may also react with aqueous nitrous acid to form 2-nitro-4-methoxyphenol and benzoquinone in varying ratios depending on the reaction conditions.
4-Methoxyphenol can be used as a building block in designing β-cyclodextrin 4-methoxyphenol conjugates that can be potential ligands for drug complexation.
4-Nitrobenzoic acid
PTBBA; 4-tert-Butylbenzoic acid; p-Tert-butylbenzoic acid; 对叔丁基苯甲酸; 4-(1,1-dimethylethyl)-Benzoic acid; Acide tert-butyl-4 benzoique CAS NO: 98-73-7
4-NONYLPHENOL

4-Nonylphenol, also known as para-nonylphenol or 4-NP, is a chemical compound that belongs to the family of alkylphenols.
4-Nonylphenol is derived from phenol where a nonyl (a nine-carbon linear alkyl) group is attached to the para position of the phenolic ring.
The chemical formula for 4-Nonylphenol is C15H24O.

CAS Number: 104-40-5
EC Number: 203-199-4

para-Nonylphenol, 4-NP, p-Nonylphenol, Nonylphenol, 4-Hydroxynonylbenzene, 4-Nonylhydroxybenzene, para-Nonylphenol, 4-Nonylphenol, branched, 4-Nonylphenol, technical grade, para-Isomer of Nonylphenol, para-Isomer of Alkylphenol, 4-Isopropylnonylphenol, Nonylphenol, para-form, p-Isomer of Nonylphenol, para-Nonylphenol isomer, Nonylphenol, isomer mixture, 4-Nonylphenol, isomer mixture, para-Nonylphenol mixture, p-Nonylphenol technical, para-Nonylphenol technical, 4-Hydroxy-N-nonylbenzene, para-Nonylhydroxybenzene, para-Nonylphenol mixture, para-Nonylphenol technical grade, 4-Nonylphenol, mixture of isomers, 4-Hydroxy-nonylbenzene, p-Nonylphenol technical grade, Alkylphenol, para isomer, 4-Nonylphenol, isomers, Nonylphenol, technical, 4-Nonylphenol mixture, isomers, 4-Nonylphenol, technical mixture, para-Nonylphenol isomer mixture, 4-Nonylphenol mixture, branched and linear, 4-Isopropyl-N-nonylphenol, 4-Isopropyl-N-nonylbenzene, 4-Nonylphenol, isomer mixtures, 4-Nonylphenol, isomer mixture, technical grade, para-Nonylphenol isomer mixture, 4-Nonylphenol mixture, isomers, 4-Nonylphenol, branched isomer



APPLICATIONS


4-Nonylphenol has been historically utilized in the production of nonylphenol ethoxylates (NPEs), which serve as surfactants in various industrial formulations.
As a surfactant, it plays a crucial role in emulsification, aiding in the dispersion of non-miscible substances in formulations such as detergents and cleaning products.

Nonylphenol ethoxylates derived from 4-Nonylphenol have been employed in textile processing for their wetting and dispersing properties.
4-Nonylphenol is utilized in certain polymerization processes, contributing to the production of specific polymers with desirable properties.

In the agricultural sector, it has found applications in pesticide formulations to enhance their effectiveness and dispersion.
4-Nonylphenol has been used in the synthesis of antioxidants, adding stability to certain products and materials.

Its surfactant properties make it valuable in the formulation of emulsifiable concentrates used in agrochemicals.
4-Nonylphenol has been employed in the manufacturing of certain industrial lubricants and cutting fluids.
4-Nonylphenol can be used in the production of specialty chemicals for applications in the petrochemical industry.

4-Nonylphenol has been explored in the development of certain adhesives and sealants for its emulsifying and wetting capabilities.
4-Nonylphenol has found applications in the production of printing inks, where its surfactant properties aid in ink dispersion.
In the leather industry, 4-Nonylphenol has been used in certain processing steps for its emulsifying properties.

4-Nonylphenol plays a role in the stabilization of certain formulations, contributing to the shelf life of products such as paints and coatings.
4-Nonylphenol has been investigated for its potential use in the synthesis of biodegradable surfactants with reduced environmental impact.

In the pharmaceutical industry, it may find application in specific formulations where its surfactant or emulsifying properties are beneficial.
Efforts have been made to explore alternative compounds with similar surfactant properties to replace 4-Nonylphenol in certain applications.
Research is ongoing to develop environmentally friendly alternatives in industries where 4-Nonylphenol has traditionally been used.

Its surfactant characteristics make it relevant in the production of emulsifiable concentrates in the formulation of agrochemicals.
4-Nonylphenol's emulsifying properties contribute to its use in certain cosmetic and personal care product formulations.
4-Nonylphenol's stability in various conditions makes it valuable in industries requiring stable formulations over time.
Studies have explored its potential role in the synthesis of specialty chemicals for applications in the production of plastics.

The use of 4-Nonylphenol in certain industrial processes necessitates responsible handling and disposal practices to prevent environmental contamination.
Ongoing research is focused on understanding and mitigating the potential environmental impact associated with its usage.
Regulatory considerations and discussions are ongoing to manage and restrict the use of 4-Nonylphenol in specific applications due to environmental and health concerns.
Awareness of the compound's properties is crucial for industries to make informed decisions about its applications, taking into account environmental sustainability and regulatory compliance.

4-Nonylphenol has been employed as an additive in certain hydraulic fluids to enhance their lubricating properties.
In the field of textile manufacturing, it finds applications in dyeing processes due to its wetting and dispersing capabilities.

4-Nonylphenol has been investigated for its potential use in the synthesis of nonylphenol-based polyesters for specific industrial applications.
4-Nonylphenol can be utilized in the formulation of certain inkjet printing inks for improved color dispersion.

4-Nonylphenol has been explored for its potential use in the synthesis of nonylphenol-based resins for coatings and adhesives.
In the production of latex-based products, 4-Nonylphenol has been used as an emulsifying agent.

Efforts are underway to explore its application in the synthesis of nonylphenol-based surfactants with reduced environmental impact.
4-Nonylphenol has been studied for its potential use in the formulation of nonylphenol-modified epoxy resins for specific industrial coatings.

4-Nonylphenol can be found in certain formulations of mold-release agents used in the manufacturing of plastics.
The compound's emulsifying properties make it relevant in the formulation of certain agrochemicals for crop protection.
In the production of certain foaming agents, 4-Nonylphenol is utilized to enhance foam stability.

4-Nonylphenol has been explored in the development of nonylphenol-based plasticizers for specific polymer applications.
4-Nonylphenol can find application in the synthesis of certain antioxidants used in the stabilization of industrial products.

4-Nonylphenol has been studied for its potential use in the formulation of nonylphenol-based lubricants for specific applications.
In the construction industry, it may be used in certain formulations for waterproofing agents.
4-Nonylphenol's emulsifying properties make it relevant in the formulation of certain emulsion polymerization processes.

4-Nonylphenol has been investigated for its potential use in the production of nonylphenol-modified thermoplastic elastomers.
4-Nonylphenol has been explored in the development of nonylphenol-based corrosion inhibitors for specific industrial applications.

In the electronics industry, 4-Nonylphenol has found applications in certain formulations for circuit board coatings.
4-Nonylphenol has been used in the formulation of certain nonylphenol-based adjuvants for agricultural applications.
4-Nonylphenol has been employed in the synthesis of certain nonylphenol-modified polyurethane foams.

4-Nonylphenol may find application in the synthesis of nonylphenol-based resins for use in the manufacturing of composites.
4-Nonylphenol's emulsifying properties make it relevant in the formulation of certain nonylphenol-based detergents.
In the leather industry, it may be used in specific formulations for leather finishing and processing.
4-Nonylphenol has been explored for its potential use in the synthesis of nonylphenol-modified silicone polymers for industrial applications.

4-Nonylphenol has been used as an emulsifying agent in the production of certain nonylphenol-based emulsions for industrial processes.
4-Nonylphenol finds application in the formulation of certain nonylphenol-modified resins used in the production of coatings and sealants.

In the field of paper and pulp production, 4-Nonylphenol may be used in certain formulations for paper sizing.
4-Nonylphenol has been studied for its potential use in the synthesis of nonylphenol-based adhesives for specific bonding applications.

4-Nonylphenol plays a role in the formulation of certain nonylphenol-based surfactants used in the cosmetics and personal care industry.
4-Nonylphenol has been explored in the development of nonylphenol-based plastic additives for enhancing polymer properties.
4-Nonylphenol may find application in the synthesis of nonylphenol-modified epoxy resins for use in the construction and automotive industries.
4-Nonylphenol has been investigated for its potential use in the formulation of nonylphenol-based antioxidants for industrial applications.

In the realm of oil and gas, it may be used in certain formulations for enhanced oil recovery processes.
4-Nonylphenol's emulsifying properties make it relevant in the formulation of certain nonylphenol-based detergents and cleaning agents.
4-Nonylphenol has been studied for its potential use in the development of nonylphenol-modified polyethylene for specific applications.

The compound may find application in the synthesis of certain nonylphenol-based dispersants used in the formulation of paints and inks.
4-Nonylphenol has been explored for its potential use in the production of nonylphenol-modified polyols for use in polyurethane foams.
It plays a role in the formulation of certain nonylphenol-based corrosion inhibitors for metal protection in industrial settings.

In wastewater treatment processes, 4-Nonylphenol has been used in certain formulations for the removal of heavy metals.
4-Nonylphenol's emulsifying properties make it relevant in the formulation of certain nonylphenol-based emulsion polymerization processes.
4-Nonylphenol may find application in the synthesis of nonylphenol-modified thermoplastic elastomers for specific industrial uses.
4-Nonylphenol has been explored in the development of nonylphenol-based plastic stabilizers for use in polymer processing.

In the electronics industry, it may be used in certain formulations for the production of nonylphenol-based conformal coatings.
4-Nonylphenol has been studied for its potential use in the synthesis of nonylphenol-modified polyethylene terephthalate for specific applications.
4-Nonylphenol has been used in the formulation of certain nonylphenol-based textile auxiliaries for fabric treatment.
4-Nonylphenol finds application in the development of nonylphenol-based hydraulic fluids for specific industrial machinery.

4-Nonylphenol may be employed in certain nonylphenol-based formulations for the preservation of wood and wood products.
In the automotive industry, 4-Nonylphenol has been explored for its potential use in the synthesis of nonylphenol-modified polymers for various components.
4-Nonylphenol's properties make it relevant in the formulation of certain nonylphenol-based specialty chemicals for specific industrial applications.



DESCRIPTION


4-Nonylphenol, also known as para-nonylphenol or 4-NP, is a chemical compound that belongs to the family of alkylphenols.
4-Nonylphenol is derived from phenol where a nonyl (a nine-carbon linear alkyl) group is attached to the para position of the phenolic ring.
The chemical formula for 4-Nonylphenol is C15H24O.

4-Nonylphenol is an organic compound with a molecular structure derived from phenol and a nine-carbon linear alkyl chain.
4-Nonylphenol is characterized by a white crystalline appearance, often seen as a fine powder or solid.
With a distinct sweet and slightly phenolic odor, 4-Nonylphenol may be recognized by its aromatic fragrance.

4-Nonylphenol is known for its hydrophobic nature, sparing solubility in water but readily dissolving in organic solvents.
4-Nonylphenol exhibits versatility as it can exist in various isomeric forms, contributing to its multifaceted applications.
4-Nonylphenol is commonly synthesized through processes involving alkylphenol ethoxylation or from nonylphenol precursors.

4-Nonylphenol's structure features a phenolic ring, imparting certain properties that make it useful in diverse industrial applications.
With a molecular weight of approximately 220.38 g/mol, 4-Nonylphenol is relatively lightweight in its solid state.
4-Nonylphenol has been employed historically in the production of nonylphenol ethoxylates, serving as surfactants in various formulations.

Due to its surfactant properties, 4-Nonylphenol contributes to emulsification and detergent capabilities in certain products.
While the compound is versatile, its use has been scrutinized due to environmental and health concerns related to its persistence and endocrine-disrupting effects.
4-Nonylphenol is known to exhibit estrogenic activity, impacting the endocrine system of aquatic organisms and wildlife.

As an alkylphenol, it is crucial to manage and regulate its usage to mitigate potential ecological and human health risks.
4-Nonylphenol has found application in the production of certain polymers, further expanding its industrial relevance.

Its stability under normal atmospheric conditions and compatibility with various materials make it suitable for specific manufacturing processes.
4-Nonylphenol is subject to regulatory scrutiny in different regions, emphasizing the importance of responsible handling and use.

4-Nonylphenol's branched isomers contribute to its unique properties, influencing its behavior in different applications.
In the context of detergents and cleaning products, 4-Nonylphenol enhances the effectiveness of these formulations.
The phenolic structure of 4-Nonylphenol contributes to its antioxidant properties in certain applications.

While it has been widely used, efforts are ongoing to explore alternative substances with lower environmental impact.
Researchers and industries are actively investigating ways to minimize the potential ecological footprint associated with 4-Nonylphenol.

4-Nonylphenol's presence in industrial processes necessitates responsible disposal methods to prevent environmental contamination.
Despite its challenges, ongoing studies aim to better understand the compound's behavior and its implications for ecosystems and human health.
4-Nonylphenol's properties make it a subject of ongoing research and regulatory discussions in various scientific and industrial communities.
A comprehensive understanding of 4-Nonylphenol's characteristics is crucial for responsible and sustainable management in industrial and environmental contexts.



PROPERTIES


Chemical Properties:

Chemical Formula: C15H24O
Molecular Weight: Approximately 220.36 g/mol
Structural Formula:
CAS Registry Number: 104-40-5
EC Number: 203-199-4


Physical Properties:

Physical State: White crystalline solid or powder
Melting Point: Varies depending on isomeric composition (ranges typically from 45 to 75 °C)
Boiling Point: Decomposes before reaching a distinct boiling point
Density: Varies based on isomer composition (typically around 0.96 - 0.98 g/cm³)
Solubility: Slightly soluble in water, soluble in organic solvents


Odor and Appearance:

Odor: Sweet and slightly phenolic
Appearance: White to off-white solid or powder



FIRST AID


Inhalation:

Remove to Fresh Air:
If inhaled, move the affected person to an area with fresh air immediately.

Seek Medical Attention:
If respiratory irritation or difficulty persists, seek medical attention promptly.


Skin Contact:
Remove Contaminated Clothing:
ake off contaminated clothing and shoes immediately.

Wash Skin Thoroughly:
Wash the affected skin with plenty of soap and water for at least 15 minutes.

Seek Medical Attention:
If irritation, redness, or other adverse effects occur, seek medical advice.


Eye Contact:

Flush with Water:
Rinse eyes with gently flowing water for at least 15 minutes, keeping eyelids open.

Remove Contact Lenses:
If applicable, remove contact lenses after the initial flushing, and continue rinsing.

Seek Medical Attention:
Seek immediate medical attention if irritation or redness persists.


Ingestion:

Do Not Induce Vomiting:
Do not induce vomiting unless directed to do so by medical personnel.

Do Not Administer Fluids:
Do not give anything by mouth to an unconscious person.

Seek Medical Attention:
Seek immediate medical attention and provide the medical personnel with detailed information.


General First Aid:

Personal Protection:
Use appropriate personal protective equipment (PPE) if providing first aid and ensure your safety.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including chemical-resistant gloves, safety goggles or face shield, and protective clothing, to minimize skin and eye contact.

Ventilation:
Work in a well-ventilated area or use local exhaust ventilation to control airborne concentrations.

Avoiding Contact:
Avoid skin contact and inhalation of vapors or mists. Use tools or equipment with protective handles when possible.

Preventing Ingestion:
Do not eat, drink, or smoke while handling 4-Nonylphenol. Wash hands thoroughly after handling.

Labeling and Identification:
Clearly label containers with the chemical name, hazard information, and appropriate safety symbols.

Preventing Cross-Contamination:
Prevent cross-contamination by segregating 4-Nonylphenol from incompatible substances.

Avoiding Mixing:
Do not mix with other chemicals unless compatibility is confirmed.

Training:
Ensure personnel are trained in the proper handling, use, and emergency procedures related to 4-Nonylphenol.

Emergency Equipment:
Have emergency equipment, including eyewash stations and safety showers, readily available.

Spill Response:
Establish procedures for spill response and clean-up. Use absorbent materials to contain and clean up spills promptly.

Waste Disposal:
Dispose of waste in accordance with local, regional, and national regulations.


Storage:

Storage Location:
Store 4-Nonylphenol in a cool, well-ventilated area away from direct sunlight and incompatible materials.

Temperature Control:
Avoid temperature extremes.
Store at temperatures within the specified range to maintain stability.

Ventilation:
Ensure adequate ventilation in storage areas to prevent the accumulation of vapors.

Storage Containers:
Use containers made of compatible materials, such as high-density polyethylene (HDPE) or glass, to store 4-Nonylphenol.

Labeling:
Clearly label storage containers with the chemical name, hazard information, and any specific storage instructions.

Segregation:
Segregate 4-Nonylphenol from incompatible substances to prevent reactions.

Security Measures:
Implement security measures to restrict access to authorized personnel only.

Regular Inspections:
Conduct regular inspections of storage areas to identify and address potential issues promptly.

Container Integrity:
Inspect storage containers regularly for signs of damage or deterioration.
Replace damaged containers promptly.

Emergency Response Planning:
Develop and communicate emergency response plans for potential incidents involving 4-Nonylphenol.

Spill Containment:
Have appropriate spill containment measures in place, including absorbent materials and spill kits.

Training:
Ensure that personnel involved in storage are trained in proper storage procedures and emergency response.

Documentation:
Maintain accurate documentation of inventory, storage conditions, and any incidents.

Regulatory Compliance:
Adhere to all relevant regulations and guidelines regarding the storage of 4-Nonylphenol.

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-Tert-Butylbenzoic Acid
4-Tert-Butylbenzoic Acid; PTBBA; p-Tert-butylbenzoic acid; 4-(1,1-dimethylethyl)-Benzoic acid; Acide tert-butyl-4 benzoique; PTBBA CAS NO: 98-73-7
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.

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.
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
ACETAMIDE MEA
ACETAMIDOETHOXYETHANOL, N° CAS :118974-46-2, ACETAMIDOETHOXYETHANOL, Acetamide, N-[2-(2-hydroxyethoxy)ethyl]-. Ses fonctions (INCI) :Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau
Acetamide
AMMONIUM ACETATE, N° CAS : 631-61-8 , Acétate d'ammonium, Nom INCI : AMMONIUM ACETATE, Nom chimique : Ammonium acetate, N° EINECS/ELINCS : 211-162-9, Additif alimentaire : E264, Ses fonctions (INCI), Régulateur de pH : Stabilise le pH des cosmétiques
Acétate d'ammonium
AMYL ACETATE, N° CAS : 628-63-7, Nom INCI : AMYL ACETATE, Nom chimique : Pentyl acetate, N° EINECS/ELINCS : 211-047-3. Ses fonctions (INCI): Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Solvant : Dissout d'autres substances. 1-Pentanol, acetate; 211-047-3 [EINECS]; Noms français : 1-PENTANOL ACETATE; 1-PENTYL ACETATE ACETATE D'AMYLE; ACETIC ACID, PENTYL ESTER; Acétate d'amyle normal; Acétate de 1-pentyle; Acétate de n-amyle; AMYL ACETATE NORMAL; n-Amyl acetate; NORMAL-AMYL ACETATE PENTANOL ACETATE; Pentyl acetate; Noms anglais :Acetic acid, amyl ester; Amyl acetate (normal-); Amyl acetic ester; Amyl acetic ether; n-Amyl acetate; n-Pentyl acetate; Normal amyl acetate Pent-acetate; Pentyl acetate, all isomers [628-63-7]; Famille chimique; Ester; Utilisation L'acétate d'amyle normal est utilisé : comme solvant dans les laques à base de nitrocellulose, les vernis, les peintures, les vernis à ongles, les parfums, les ciments et les lampes fluorescentes; comme solvant dans l'industrie photographique (pellicules) et dans l'industrie textile (soie, cuir artificiel); comme nettoyant de taches dans l'industrie du nettoyage à sec; comme agent de saveur dans l'industrie alimentaire; dans l'industrie pharmaceutique. 628-63-7 [RN] Acétate de pentyle [French] Acetic acid n-amyl ester Acetic acid n-pentyl ester Acetic acid, n-pentyl ester Acetic acid, pentyl ester Amyl Acetate Amyl acetate, n- n-Pentyl acetate n-PENTYL ETHANOATE Pentyl acetate Pentyl ethanoate Pentylacetat Pentyl-acetat [German] 1-Acetoxypentane 1-Pentanol acetate 1-Pentyl acetate Acetate d'amyle [French] Acetic acid amyl ester Acetic acid pentyl ester Acetic acid, amyl ester Acetic acid, N-amyl ester Amyl acetate211-047-3MFCD00009500 Amyl acetic ester Amyl acetic ether Amylacetate Amylazetat [German] Amylester kyseliny octove [Czech] banana oil [Wiki] Birnenoel N-Amyl acetate Octan amylu [Polish] Pear oil Pent-acetate pentanol acetate Prim-amyl acetate Primary amyl acetate
ACETATE D'AMYLE ( AMYL ACETATE)
BENZYL ACETATE, N° CAS : 140-11-4 / 101-41-7, Nom INCI : BENZYL ACETATE. Nom chimique : Methyl Phenylacetate; Methyl alpha-Toluate. N° EINECS/ELINCS : 205-399-7 / 202-940-9. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques
Acétate de benzyle ( BENZYL ACETATE)
BUTYL ACETATE, N° CAS : 123-86-4 - Acétate de butyle, Origine(s) : Synthétique. Nom INCI : BUTYL ACETATE. Nom chimique : n-Butyl acetate. N° EINECS/ELINCS : 204-658-1. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Solvant : Dissout d'autres substances
Acétate de butyle
propan-2-yl 2-methoxyacetate
ACÉTATE DE MÉTHOXYISOPROPYLE
POTASSIUM ACETATE, N° CAS : 127-08-2 - Acétate de potassium, Nom INCI : POTASSIUM ACETATE. Nom chimique : Potassium acetate. N° EINECS/ELINCS : 204-822-2. Additif alimentaire :E261, Ses fonctions (INCI), Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles
Acétate de potassium
STRONTIUM ACETATE, N° CAS : 543-94-2 - Acétate de strontium (hémihydraté), Nom INCI : STRONTIUM ACETATE, Nom chimique : Strontium di(acetate), N° EINECS/ELINCS : 208-854-8 Classification : Règlementé. Ses fonctions (INCI) : Agent d'hygiène buccale : Fournit des effets cosmétiques à la cavité buccale (nettoyage, désodorisation et protection). Agent apaisant : Aide à alléger l'inconfort de la peau ou du cuir chevelu
Acétate de strontium (hémihydraté)
Acétate de la vitamine E (+); Acétate de vitamine E; ALPHA-TOCOPHEROL ACETATE (+); D-.ALPHA.-TOCOPHERYL ACETATEalpha-Tocopherol acetate; tocopherol acetate; α-tocopheryl acetate; TOCOPHERYL ACETATE, N° CAS : 7695-91-2 / 58-95-7 - Acétate de tocophérol, Origine(s) : Végétale, Synthétique. Autres langues : Acetato de tocoferilo, Acetato di tocoferile, Tocopherylacetat, Nom INCI : TOCOPHERYL ACETATE. Nom chimique : 3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-yl acetate, N° EINECS/ELINCS : 231-710-0 / 200-405-4. L'acétate de tocophérol est un dérivé de Vitamine E. Il agit dans les cosmétiques en tant qu'antioxydant. Il peut être produit synthétiquement ou d'origine naturel, extrait d'huile de Soja ou de tournesol par exemple. Il est souvent utilisé dans les cosmétiques en tant qu'alternative au tocophérol pur, parce qu'il est considéré plus stable et moins acide. Il est autorisé en bio, lorsqu'il est d'origine végétal.Ses fonctions (INCI) : Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Agent d'entretien de la peau : Maintient la peau en bon état; (+)-α-Tocopherol acetate (2R)-2,5,7,8-Tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-chromen-6-yl acetate [ACD/IUPAC Name] (2R)-2,5,7,8-Tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-chromen-6-yl-acetat [German] [ACD/IUPAC Name] [2R*(4R*,8R*)]-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol Acetate 200-405-4 [EINECS] 231-710-0 [EINECS] 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-, acetate, (2R)- [ACD/Index Name] 58-95-7 [RN] 7695-91-2 [RN] A7E6112E4N Acétate de (2R)-2,5,7,8-tétraméthyl-2-[(4R,8R)-4,8,12-triméthyltridécyl]-3,4-dihydro-2H-chromén-6-yle [French] [ACD/IUPAC Name] all-rac-α-tocopheryl acetate a-Tocopherol Acetate a-Tocopheryl Acetate D-?-tocopherol acetate Eprolin [Trade name] E-Vimin Evion GA8747000 GP8280000 MFCD00072042 [MDL number] MFCD00072052 O-Acetyl-α-tocopherol TOCOPHEROL ACETATE [JP15] Tocopheryl acetate [Wiki] Tocopheryl Acetate, a Vitamin E acetate Vitamin- E acetate α Tocopheryl Acetate α-Tocopherol acetate α-Tocopherylis acetas α-Tocopherol acetate ()-α-Tocopherol acetate (?)-?-Tocopheryl acetate (+)-?-Tocopherol acetate (+)-α-tocopherol acetate (2R-(2R*(4R*,8R*)))-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol acetate (2R*(4R*,8R*))-(1)-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-yl acetate [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-yl] acetate [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] acetate [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] ethanoate [(2S)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] acetate [(2S)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] ethanoate [2R*(4R*,8R*)]-()-3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-yl acetate [58-95-7] [7695-91-2] 133-80-2 [RN] 1407-18-7 [RN] 18920-61-1 [RN] 2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-chromen-6-yl acetate [ACD/IUPAC Name] 200-412-2 [EINECS] 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)-, acetate, (2R)- 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)-, acetate, (2R)-rel- 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, acetate, [2R-[2R*(4R*,8R*)]]- 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, acetate,(2R*(4R*,8R*))-(±)- 2H-1-Benzopyran-6-ol,3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-,6-acetate, (2R)-rel- 3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-b- enzopyran-6-ol, acetate 3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-yl acetate 5-17-04-00169 [Beilstein] 5-17-04-00169 (Beilstein Handbook Reference) [Beilstein] 54-22-8 [RN] 6-acetoxy-2,5,7,8-tetramethyl-2-(4',8',12'-trimethyltridecyl)-chromane 6-Chromanol, 2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, acetate Acetic acid (R)-2,5,7,8-tetramethyl-2-((4R,8R)-4,8,12-trimethyl-tridecyl)-chroman-6-yl ester acetic acid [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-6-chromanyl] ester acetic acid [(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] ester acetic acid [(2S)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-6-chromanyl] ester acetic acid [(2S)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] ester Acetic acid 2,5,7,8-tetramethyl-2-(4,8,12-trimethyl-tridecyl)-chroman-6-yl ester Alfacol all-rac-2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-1-benzopyran-6-yl acetate all-rac-α-Tocopheryl acetate Contopheron d-??Tocopheryl Acetate d-a-tocopheryl acetate DL-??-Tocopherol Acetate DL-?-Tocopherol Acetate DL-��-Tocopherol Acetate DL-α-Tocopherol acetate DL-α-Tocopheryl acetate DL-��-Tocopherol Acetate DL-α-Tocopherol acetate, 50% powder form DL-α-Tocopherol acetate, EP/USP/FCC grade DL-α-Tocopherylacetate (Vitamin E acetate) D-α tocoferil acetate d-α Tocopheryl Acetate d-α-tocopherol acetate D-α-Tocopherol Acetate D-α-TOCOPHEROLACETATE D-α-Tocopheryl acetate d-α-tocopheryl acetate, 97% Ecofrol ECON E-ferol EINECS 231-710-0 EINECS 257-757-7 Endo E dompe Ephynal Epsilan-M E-Toplex Evipherol Fertilvit Gevex α-Tocopherol Acetate α-Tocopherylis acetas Juvela [Trade name] NCGC00166253-01 O-Acetyl-α-tocopherol Rovimix E 50SD RRR-α-tocopheryl acetate Syntopherol acetate Tocopherex Tocopherol acetate (JP15) Tocopherolacetate, α- Tocophrin TOFAXIN UNII:A7E6112E4N UNII-A7E6112E4N UNII-WR1WPI7EW8 Vectan Vectan (TN) vitamin e acetate 96% Vitamin E Acetate Oil - Synthetic Vitamin E acetate, d- vitamin e acetate α-tocopherol acetate α-Tocopherol acetate, all rac α-TOCOPHEROL ACETATE, D- α-TOCOPHEROL ACETATE, DL- α-Tocopheryl acetate α-Tocopheryl acetate α-tocopheryl acetate, D-
Acétate de tocophérol ( TOCOPHERYL ACETATE)
ZINC ACETATE N° CAS : 557-34-6 - Acétate de zinc "Satisfaisant" dans toutes les catégories. Nom INCI : ZINC ACETATE Nom chimique : Zinc di(acetate) N° EINECS/ELINCS : 209-170-2 Additif alimentaire : E650 Classification : Règlementé Restriction en Europe : III/24 La concentration maximale autorisée en cosmétique est la suivante : 1 % (en zinc). Ses fonctions (INCI) Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes
Acétate de zinc ( ZINC ACETATE)
CETYL ACETATE, N° CAS : 629-70-9, Nom INCI : CETYL ACETATE, Nom chimique : Hexadecyl acetate, N° EINECS/ELINCS : 211-103-7, Emollient : Adoucit et assouplit la peau, Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit, Agent d'entretien de la peau : Maintient la peau en bon état; Hexadecyl acetate; 1-Hexadecanol, 1-acetate; Cetyl acetate; Cetyl acetate 1-Hexadecanol, acetate [ACD/Index Name]; Acétate d'hexadécyle [French] ; Cetyl alcohol acetate; Hexadecyl acetate ; Hexadecyl-acetat [German] ; 1-Acetoxyhexadecane; 1-Hexadecanol acetate; 1-Hexadecanol, 1-acetate; 1-Hexadecyl acetate; Acelan A; acetic acid cetyl ester; acetic acid hexadecyl ester; Acetic acid, hexadecyl ester; CETYL ACETATE|HEXADECYL ACETATE; Hexadecanol acetate; Hexadecanyl acetate; hexadecyl ethanoate; n-Hexadecyl acetate; n-Hexadecyl ethanoate; Palmityl acetate
Acétate d'hexadécyle ( CETYL ACETATE)
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
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 chloride
Nom INCI : ACETYL CYSTEINE Nom chimique : Acetylcysteine N° EINECS/ELINCS : 210-498-3 Ses fonctions (INCI) Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité Agent d'entretien de la peau : Maintient la peau en bon état
ACETYL CYSTEINE (N° CAS : 616-91-1)
Nom INCI : ACETYL GLUTAMIC ACID Nom chimique : N-acetylglutamic acid N° EINECS/ELINCS : 214-708-4 Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état
ACETYL GLUTAMIC ACID (N° CAS : 1188-37-0)
Nom INCI : ACETYL TRIETHYL CITRATE Nom chimique : Triethyl 2-acetoxy-1,2,3-propanetricarboxylate N° EINECS/ELINCS : 201-066-5 Ses fonctions (INCI) Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit Agent plastifiant : Adoucit et rend souple une autre substance qui autrement ne pourrait pas être facilement déformée, dispersée ou être travaillée Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques
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.
ACETYL TRIETHYL CITRATE (N° CAS : 77-89-4)
Nom INCI : ACETYL TRIETHYLHEXYL CITRATE Nom chimique : Tris(2-ethylhexyl) 2-(acetyloxy)propane-1,2,3-tricarboxylate N° EINECS/ELINCS : 205-617-0 Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles Agent plastifiant : Adoucit et rend souple une autre substance qui autrement ne pourrait pas être facilement déformée, dispersée ou être travaillée Agent d'entretien de la peau : Maintient la peau en bon état
ACETYL TRIETHYLHEXYL CITRATE ( N° CAS : 144-15-0)
Nom INCI : ACETYLATED LANOLIN N° EINECS/ELINCS : 262-979-2 Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Emollient : Adoucit et assouplit la peau Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance Agent d'entretien de la peau : Maintient la peau en bon état
ACETYLATED LANOLIN ( N° CAS : 61788-48-5 - Lanoline acétylée)
ACIDE GLYOXYLIQUE; GLYOXYLIC ACID, N° CAS : 298-12-4, Nom INCI : GLYOXYLIC ACID, Nom chimique : Glyoxylic acid, N° EINECS/ELINCS : 206-058-5. Ses fonctions (INCI): Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Régulateur de pH : Stabilise le pH des cosmétiques. Agent bouclant ou lissant (coiffant) : Modifie la structure chimique des cheveux, pour les coiffer dans le style requis. Noms français : ACIDE GLYOXYLIQUE. Noms anglais : ACETIC ACID, OXO-; GLYOXYLIC ACID. 1209322 [Beilstein]; 201-180-5 [EINECS]; 2-Hydroxyethanoic acid; 79-14-1 [RN]; Acetic acid, 2-hydroxy- [ACD/Index Name]; Acide glycol [French] [ACD/IUPAC Name]; Acide hydroxyacétique [French]; a-Hydroxyacetic acid Glycol acid [ACD/IUPAC Name]; Glycolsäure [German]; Hydroxyessigsäure [German] [ACD/IUPAC Name]; Kyselina glykolova [Czech]; Kyselina hydroxyoctova [Czech]; QV1Q [WLN] 1,2-Ethanediol [ACD/Index Name]; 102962-28-7 [RN]; 1-hydroxy-ethanoic acid; 26009-03-0 [RN]; 2-oxonioacetate; 4-03-00-00571 (Beilstein Handbook Reference) [Beilstein];Acetate ion Acetic acid [ACD/Index Name] [ACD/IUPAC Name]; D(-)-TARTARIC ACID; D-malate; EDO; GLV; Glycocide; Glycolic acid, 66-70% aqueous solution; glycolic acid, crystal, reagent;Glycolic acid, pure, 99.5%; Glycollic acid; Glyoxylic acid [Wiki]; GOA; HOCH2COOH; Hydroxy-acetic acid; Hydroxyethanoic acid; Kyselina glykolova; MFCD00868116 [MDL number]; MLT; TAR;WLN: QV1Q α-Hydroxyacetic acid; α-Hydroxyacetic acid; 乙醇酸 [Chinese]. Glyoxylic acid. CAS names; Acetic acid, 2-oxo-. : 2-oxo acetic acid; 2-oxoacetic acid; glyocylic acid; glyoxyl acid ; Glyoxylic Acid (ca. 50% in Water, ca. 9mol/L); Glyoxylic Acid 50% (aqueous solution); oxaldehydic acid; oxoacetic acid; oxoethanoic acid. Trade names: Glyoxylic acid 50 % (aqueous solution); Glyoxylic acid liq 50
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.
ACIDE GLYOXYLIQUE ( Glyoxylic acid)
Acide 2-aminoéthanesulfinique; N° CAS : 300-84-5; Hypotaurine; Nom INCI : AMINOETHANESULFINIC ACID. Nom chimique : Ethanesulfinic acid, 2-amino-. Ses fonctions (INCI): Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Agent réducteur : Modifie la nature chimique d'une autre substance en ajoutant de l'hydrogène ou en éliminant l'oxygène. 2-amino-Ethanesulfinic acid; 2-Aminoethanesulfinic acid ; 2-Aminoethansulfinsäure [German] ; 2-Aminoethylsulfinate; 2-Aminoethylsulfinic acid; 300-84-5 [RN]; Acide 2-aminoéthanesulfinique [French] ; Ethanesulfinic acid, 2-amino- ; Hypotaurine; MFCD00038197; 2-amino-Ethanesulfinate 2-Aminoethanesulfinate ; Cystaminesulfinate; Cystaminesulfinic acid; 2-aminoethane-1-sulfinic acid; 2-aminoethanesulfinicacid; 2-azaniumylethane-1-sulfinate; 2-azaniumylethanesulfinate; 2-mmonioethane-1-sulfinate; hypotaurine zwitterion; Hypotaurine; 2-Aminoethylsulfinic acid; 2-Amino-ethanesulfinic acid; Lopac0_000573. Product Uses3,4 2-Amino-2-ethyl-1,3-propanediol is useful in a variety of applications, such as: Paints – as a dispersant for pigments, offering improved flow characteristics, stable pH values, low odor, and improved color; Additives – to control alkalinity and the release of excess formaldehyde in certain industrial situations, such as metal-working fluids; A chemical intermediate – to produce fatty acid emulsifiers (several industrial applications), oxazoline chemicals (surface-active compounds) and oxazolidine (cross-linkers in thermosetresins)
Acide 2-aminoéthanesulfinique (AMINOETHANESULFINIC ACID)
BUTYLOCTANOIC ACID, 2-butyloctanoic acid; Octanoic acid, 2-butyl-; Isocarb 12; N° CAS : 27610-92-0, Nom INCI : BUTYLOCTANOIC ACID, Nom chimique : 2-Butyloctanoic acid, N° EINECS/ELINCS : 248-570-1; Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile).Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. 248-570-1 [EINECS] 27610-92-0 [RN]; 2-Butyloctanoic acid ; 2-Butyloctansäure [German] ; Acide 2-butyloctanoïque [French] ;BUTYLOCTANOIC ACID ; Octanoic acid, 2-butyl- [ACD/Index Name]; 2-Butyloctanedioic acid ; 2-BUTYLOCTANOICACID; 2-Butyloctansaeure [German]; 2-Butyloctansaeure;4-02-00-01112 [Beilstein] 50905-10-7 [RN]; 53687-45-9 [RN]; 5-Undecanecarboxylic acid;PI-46872
Acide 2-butyloctanoïque ( Butyloctanoic acid)
Acide acrylique ; N° CAS : 79-10-7, Nom INCI : ACRYLIC ACID; N° EINECS/ELINCS : 201-177-9;2-PROPENOIC ACID; Acide acrylique. Noms anglais :ACROLEIC ACID; Acrylic acid; ETHYLENE CARBOXYLIC ACID; PROPENOIC ACID; VINYL FORMIC ACID; VINYLFORMIC ACID. Utilisation: Fabrication de produits organiques. fabrication de polymères Ses fonctions (INCI) : Agent d'entretien des ongles : Améliore les caractéristiques esthétiques des ongles. 2-Propenoic acid Acido acrilio; Acroleic acid; Acrylic acid;Acrylic acid, glacial; ACRYLIC ACID, STABILIZED; EU. ADN Dangerous Goods Lists, Directive 2008/68/EC, EU. ADR Dangerous Goods Lists, Directive 2008/68/EC, EU. RID Dangerous Goods Lists, Directive 2008/68/EC; acrylic acid; prop-2-enoic acid; EU. Worker Protection-Hazardous (98/24), EU. Workplace Signs, EU. Hazardous Waste Properties: Annex III (2008/98/EC), EU. Young People at Work (94/33); Ethylenecarboxylic acid; Glacial acrylic acid; Kyselina akrylova; Prop-2-enoic acid; Propene acid; Propenoic acid; Vinylformic acid; 2-propeno rūgštis (lt); 2-propensyra (sv); 2-propensyre (no); acid acrilic (ro); acid prop-2-enoic (ro); acide acrylique (fr); acido acrilico (it); acrylsyre (da); Acrylsäure (de); acrylzuur (nl); akrilna kiselina (hr); akrilna kislina (sl); akrilo rūgštis (lt); akrilsav (hu); akrilskābe (lv); akrylová kyselina (cs); akrylsyra (sv); akrylsyre (no); Akryylihappo (fi); Akrüülhape (et); kwas akrylowy (pl); kwas etenokarboksylowy (pl); kwas propenowy (pl); kyselina akrylová (sk); kyselina propénová (sk); Prop-2-eenhape (et); Prop-2-eenihappo (fi); prop-2-enojska kislina (sl); prop-2-enonska kiselina (hr); prop-2-enová kyselina (cs); prop-2-énsav (hu); Propensäure (de); propēn-2 skābe (lv); ácido 2-propenoico (es); ácido 2-propenóico (pt); ácido acrílico (es); ακρυλικο οξύ (el); акрилова киселина (bg); проп-2-енова киселина (bg) 2-hydroxyethyl methacrylate; Acrylic Acid (stabilized with MEHQ); Acrylic acid ; acrylic acid, acrylic acid glacial, acrylic acid technical; acrylicacid; prop-2-enoate
Acide acrylique ( ACRYLIC ACID)
N° CAS : 124-04-9 ; EC / List no.: 204-673-3; Mol. formula: C6H10O4; 1,4-Butanedicarboxylic acid; 1,6-Hexanedioic acid; Acifloctin; Acinetten; Adilactetten; Adipate;Adipic acid; Adipinic acid; Adipinsaure; Kyselina adipova; Molten adipic acid; acid adipic (ro); acide adipique (fr); acido adipico (it); Adipiinhape (et); Adipiinihappo (fi); adipinezuur (nl); adipinsav (hu); adipinska kiselina (hr); adipinska kislina (sl); adipinsyra (sv); adipinsyre (da); Adipinsäure (de); adipo rūgštis (lt); adipová kyselina (cs); adipīnskābe (lv); hexandikarboxylsyra (sv); kwas adypinowy (pl); kwas butano-1,4-dikarboksylowy (pl); kyselina adipová (sk); ácido adípico (es); αδιπικό οξύ (el); адипинова киселина (bg) Hexanedioic acid; : 1, 4-butanedicarboxylic acid; 1,4-buthanediacetic acid; Adipic acid ,CAS N°124-04-9; Hexamethylenediamine-adipate; hexan-1,6-dioic acid; hexane-1,6-dioic acid; Hexanedioic acid / Adipic acid; Adipic acid (8CI); adipin saure; ADIPINSAEURE L'acide adipique ou acide 1,6-hexanedioïque est un diacide carboxylique aliphatique. Il est utilisé principalement pour la fabrication du nylon, et plus généralement pour la synthèse des polyamides. C'est également un additif alimentaire (E355) utilisé pour acidifier des boissons non alcoolisées ou contrôler l’acidité des cosmétiques. Il contribue aussi au goût acide des betteraves. De formule CO2H(CH2)4CO2H, il se présente sous forme d'un solide cristallisé blanc. Il possède un groupe acide à ses 2 extrémités, comme l’acide téréphtalique, avec possibilité de développer des chaînes à chacune de ses extrémités. Par estérification avec un alcool double, tel l’éthylène glycol, il formera un polyester. Il peut également donner un polyamide.
Acide aminoethylphosphinique ( AMINOETHYLPHOSPHINIC ACID)
ASCORBIC ACID, N° CAS : 50-81-7 / 62624-30-0 - Acide ascorbique (Vitamine C),utres langues : Acido ascorbico, Askorbinsäure, Ácido ascórbico, Nom INCI : ASCORBIC ACID; Nom chimique : Ascorbic acid, N° EINECS/ELINCS : 200-066-2 / 263-644-3. Additif alimentaire : E300, Plus connu sous le nom de Vitamine C, l'acide ascorbique est utilisé en cosmétique pour ses propriétés antioxydantes. On le retrouve assez régulièrement dans les actifs anti-âge, puisque qu'il protège les cellules des dégâts causés par les radicaux libres et unifie le teint. Il est aussi présent dans de nombreux autres produits de soin pour ces propriétés. Il est présent sous forme naturel dans les fruits et légumes (citrons, oranges, kiwis ...)Ses fonctions (INCI): Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Régulateur de pH : Stabilise le pH des cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Agent d'entretien de la peau : Maintient la peau en bon état. Noms français :3-KETO-L-GULFURANOLACTONE; 3-OXO-L-GULOFURANOLACTONE; Acide ascorbique; L(+)-ASCORBIC ACID; L-3-KETOTHREOHEXURONIC ACID LACTONE; L-ASCORBIC ACID; L-LYXOASCORBIC ACID; L-TREO-HEX-ENONIC ACID, GAMMA-LACTONE; L-XYLOASCORBIC ACID; VITAMINE C XYLOASCORBIC ACID, L-. Noms anglais : Ascorbic acid; VITAMIN C. Utilisation: Vitamine. Ascorbic acid ; Vitamin C ; (5R)-5-[(1S)-1,2-Dihydroxyethyl]-3,4-dihydroxy-2(5H)-furanon [German]; (5R)-5-[(1S)-1,2-Dihydroxyethyl]-3,4-dihydroxy-2(5H)-furanone; (5R)-5-[(1S)-1,2-Dihydroxyéthyl]-3,4-dihydroxy-2(5H)-furanone; (5R)-5-[(1S)-1,2-Dihydroxyethyl]-3,4-dihydroxyfuran-2(5H)-one; 200-066-2 [EINECS]; acide ascorbique [French]; acido ascorbico [Spanish]; ácido ascórbico [Spanish]; acidum ascorbicum [Latin]; Ascorbinsäure [German]; Calscorbate; Cetebe; L-AA; L-Ascorbic acid; L-Threoascorbic acid; monodehydro-L-ascorbic acid; аскорбиновая кислота [Russian]; حمض أسكوربيك [Arabic]; 抗坏血酸 [Chinese]; (+)-ascorbate; (+)-Ascorbic acid; (2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one; (5R)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2,5-dihydrofuran-2-one (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one; [(2R)-2-(1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydrofuran-3-yl]oxidanyl; 16351-10-3 [RN]; 2-(1,2-Dihydroxyethyl)-4,5-dihydroxyfuran-3-one; 299-36-5 [RN]; 3-Keto-L-gulofuranolactone; 3-Oxo-L-gulofuranolactone; 3-Oxo-L-gulofuranolactone (enol form); 5-(1,2-Dihydroxy-ethyl)-3,4-dihydroxy-5H-furan-2-one; acidum ascorbinicum; Adenex; AHI; Allercorb; Antiscorbic vitamin; Arco-cee; ASC; Ascoltin; Ascorb; Ascor-B.I.D.; Ascorbajen; Ascorbic Acid DC97SF; ascorbicab; Ascorbicap; Ascorbicin Ascorbin; Ascorbutina; Ascorin; Ascorteal; Ascorvit; ascrobin; Cantan; Cantaxin; Catavin C; ce lent; Cebicure; Cebid []; Cebion; Cebione; Cee-caps TD; Cee-vite; Cegiolan; Ceglion Celaskon; Cell C; Cemagyl; Ce-Mi-Lin; Cemill; Cenetone; Cenolate; Cereon; Cergona; Cescorbat; Cetamid; cetane; Cetane-Caps TC; Cetane-caps TD; Cetemican; Cevalin; Cevatine; Cevex; Cevi-bid; CeviminCE-VI-Sol; Cevital; Cevitamate; Cevitamic acid; Cevitamin; Cevitan; Cevitex; Cewin; Chewcee; Ciamin; Cipca; Citriscorb; Citrovit; C-Level; C-Long; Colascor; Concemin; C-Quin; C-Span; C-Vimin; Davitamon C; D-Isoascorbic acid; Dora-C-500; Duoscorb; E300; E-300; Hicee; Hybrin; IDO-C; Juvamine; Kangbingfeng; l-​(+)​-​ascorbic acid; L(+)-ascorbate; L-(+)-ascorbate; L-(+)-ascorbic acid; l(+)-ascorbic acid standard; l,3-ketothreohexuronic acid; Laroscorbine; L-ascorbate; L-Ascorbate;Vitamin C; L-ASCORBIC ACID 2-(DIHYDROGEN PHOSPHATE) CALCIUM SALT (2:3); l-ascorbic acid (vitamin c); L-Ascorbic acid ACS reagent grade; L-ASCORBIC ACID-6,6-Dl-ascorbic acid-用于细胞培养; Lemascorb; Liqui-Cee; L-lyxoascorbate; L-Lyxoascorbic acid; L-threo-Ascorbic acid; L-threo-hex-2-enono-1,4-lactone; L-xyloascorbate; L-XYLOASCORBIC ACID; meilun; Meri-C; Natrascorb; Natrascorb injectable; Planavit C; Proscorbin; Redoxon []; Ronotec 100; Rontex 100; Roscorbic; Rovimix C; Scorbacid; Scorbu C; Scorbu-C; Secorbate; Semidehydroascorbate; Semidehydroascorbic acid; Suncoat VC 40; Testascorbic; Vasc; Vicelat; Vicin; Vicomin C; Viforcit; Viscorin; Vitace; Vitacee; Vitacimin; Vitacin; Vitamisin; Vitascorbol; Xitix; γ-lactone L-threo-Hex-2-enonate; γ-lactone L-threo-Hex-2-enonic acid
Acide ascorbique (Vitamine C)
Acide aspartique (dl-); Acide DL-aspartique. Noms anglais :Aspartic acid, DL-; dl-Aspartic acid. Utilisation: Produit organique; ASPARTIC ACID, N° CAS : 56-84-8 / 617-45-8 - Acide aspartique, Nom INCI : ASPARTIC ACID, Nom chimique : Aspartic acid, N° EINECS/ELINCS : 200-291-6 / 210-513-3.Nom UICPA acide (2S)-2-aminobutanedioïque; Synonymes : D, Aspacide 2-aminosuccinique L’acide aspartique (abréviations IUPAC-IUBMB : Asp et D), est un acide α-aminé dont l'énantiomère L est l'un des 22 acides aminés protéinogènes, encodé sur les ARN messagers par les codons GAU et GAC. Il est caractérisé par la présence d'un groupe carboxyle –COOH à l'extrémité de sa chaîne latérale, lui conférant un point isoélectrique de 2,77, ce qui en fait le résidu le plus acide dans les protéines. Ses fonctions (INCI): Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Agent d'entretien de la peau : Maintient la peau en bon éta.Acid D,L-aspart; Aspartic acid; 2-Aminobutanedioic acid DL-Aspartic acid (±)-2-Aminosuccinic acid (±)-2-Aminosuccinic acid (R,S)-Aspartic acid 200-291-6 [EINECS] 2-Aminobutandisäure [German] 2-Aminosuccinic acid 617-45-8 [RN] 774618 [Beilstein] acide 2-aminobutanedioïque [French] Acide 2-aminosuccinique [French] Acide aspartique [French] Aminosuccinic acid ASP Asparaginic acid Asparaginsäure [German] Aspartic acid Aspartic acid, D- ASPARTIC ACID, DL- DL-2-Aminobutanedioic acid DL-Aminosuccinic acid DL-Asparagic acid H-DL-Asp-OH α-Aminosuccinic acid (±)-Aspartic Acid (±)-Aspartic Acid 1-deoxy-1-(N6-lysino)-D-fructose 217-234-6 [EINECS] 2-Amino Maleic Acid 2-aminobutanedioic acid 2-azaniumyl-4-hydroxy-4-oxobutanoate 874742-68-4 secondary RN [RN] DL-Asp-OH DL-Asp-OH|2-Aminosuccinic acid H-Asp-OH MFCD00063081 [MDL number] N-acetyl-seryl-aspartate
Acide aspartique ( Aspartic acid )
AZELAIC ACID, N° CAS : 123-99-9 - Acide azélaïque, Nom INCI : AZELAIC ACID, Nom chimique : Nonanedioic acid, N° EINECS/ELINCS : 204-669-1, Régulateur de pH : Stabilise le pH des cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Noms français :1,7-HEPTANEDICARBOXYLIC ACID; ACIDE AZELAIQUE; ACIDE; HEPTANEDICARBOXYLIQUE-1,7; ACIDE NONANEDIOIQUE; HEPTANEDICARBOXYLIC ACID; NONANEDIOIC ACID. Noms anglais : ANCHOIC ACID; AZELAIC ACID;LEPARGYLIC ACID Utilisation: Fabrication de produits organiques et de résines. 1,7-Heptanedicarboxylic acid; 123-99-9 [RN]; 204-669-1 [EINECS]; Acide azélaïque [French] ; acide nonanedioïque [French]; Acido azelaico [Spanish]; anchoic acid; Azalaic Acid; Azelaate [; Azelaic acid ; Azelainic acid; Azelainsäure [German] ; Azelex ; Finaceae; lepargylic acid; Nonandisäure [German]; Nonanedioic acid Skinoren ; 1,7-dicarboxyheptane; 1,9-NONANEDIOIC ACID; acide azelaique [French]; Acido azelaico [Spanish]; Acidum acelaicum Acidum azelaicum [Latin] AHI AZ1 azelaicacid Azelainsäure Azelate Emery's L-110 Finacea Heptanedicarboxylic acid n-nonanedioic acid Nonandisäure Nonanedioate Nonanedionic acid Skinorem Zumilin
Acide azélaïque ( Azelaic acid )
Acide benzènesulfonique, dérivés mono-alkyles en C10-14; Noms anglais :Benzenesulfonic acid, mono-C10-14-alkyl derivativesC10-14 ALKYL BENZENESULFONIC ACID, N° CAS : 85117-49-3, Nom INCI : C10-14 ALKYL BENZENESULFONIC ACID, N° EINECS/ELINCS : 285-599-9. Agent nettoyant : Aide à garder une surface propre. Agent moussant : Capture des petites bulles d'air ou d'autres gaz dans un petit volume de liquide en modifiant la tension superficielle du liquide. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Benzenesulfonic acid, mono-C10-14-alkyl derivs;
Acide benzènesulfonique, dérivés mono-alkyles en C10-14 ( C10-14 ALKYL BENZENESULFONIC ACID)
BENZOIC ACID, N° CAS : 65-85-0 - Acide benzoïque. Autres langues : Acido benzoico, Benzoesäure, Ácido benzoico. Nom INCI : BENZOIC ACID. Nom chimique : Benzoic acid; N° EINECS/ELINCS : 200-618-2.Principaux synonymes. Noms français : Acide benzoique; Acide benzoïque;Benzenecarboxylic acid; Benzeneformic acid; Benzenmethanoic acid; Carboxybenzene Phenyl carboxylic acid; Phenyl formic acid; Phenylcarboxylic acid; Phenylformic acid. Noms anglais : Benzoic acid; Dracylic acid. L'acide benzoïque, de formule chimique C6H5COOH (ou C7H6O2) est un acide carboxylique aromatique dérivé du benzène.Il est utilisé comme conservateur alimentaire et est naturellement présent dans certaines plantes. C'est par exemple l'un des principaux constituants de la gomme benjoin, utilisée dans des encens dans les églises de Russie et d'autres communautés orthodoxes. Bien qu'étant un acide faible, l'acide benzoïque n'est que peu soluble dans l'eau du fait de la présence du cycle benzénique apolaire. On trouve de l'acide benzoïque dans les plantes alimentaires : - en quantité notable dans le canneberge d'Amérique11 (Vaccinium macrocarpon) : 48,10 mg·100ml-1. - dans une moindre mesure dans la poudre de cacao (Theobroma cacao) : 0,06 mg·100ml-1. Parmi les principaux composés qui dérivent de l'acide benzoïque, on peut citer l'acide salicylique et l'acide acétylsalicylique plus connu sous le nom d'aspirine. En tant qu'additif alimentaire, il est référencé en Europe sous le code E210. Ses sels, que l'on appelle des benzoates, sont référencés sous les numéros : E211 Benzoate de sodium (Ba) E212 Benzoate de potassium (Ba) E213 Benzoate de calcium (Ba) Au-dessus de 370 °C, il se décompose en formant du benzène et du dioxyde de carbone. L'acide benzoïque a une odeur forte et est facilement inflammable. Utilisation: Agent de préservation alimentaire, fabrication de produits organiques Additif alimentaire : E210. L'acide benzoïque est utilisé en tant que conservateur dans les cosmétiques. Agent de foisonnement : Réduit la densité apparente des cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Acid benzoic (ro) Acide benzoïque (fr) Acido benzoico (it) Aċidu benżojku (mt) Bensoehape (et) Bensoesyra (sv) Bentsoehappo (fi) Benzenkarboksirūgštis (lt) Benzoe-säure (de) Benzoesav (hu) Benzoesyre (da) Benzoic acid (no) Benzojeva kiselina (hr) Benzojska kislina (sl) Benzoová kyselina (cs) Benzoskābe (lv) benzosyre (no) Benzoëzuur (nl) Kwas benzoesowy (pl) Kyselina benzoová (sk) Ácido benzoico (es) Βενζοϊκό οξύ (el) Бензоена киселина (bg) benzene carboxylic acid Benzenecarboxylic acid Benzoesäure Benzoic Acid Phenylformic acid, Benzene carboxylic acid Acide benzoique [French] Acide benzoïque [French] Acido benzoico [Italian] Acidum benzoicum [Latin] Alcohol bencílico [Spanish] Benzenecarboxylic acid benzeneformic acid Benzenemethanoic acid Benzoesaeure [German] Benzoesäure [German] Benzoic acid [ACD/Index Name] [USP] [Wiki] 苯甲酸 [Chinese] Acidum benzoicum benzenemethonic acid Benzoic acid 100 µg/mL in Acetone Benzoic acid, ACS reagent Carboxybenzene DB03793 Diacylic acid Dracylic acid Euxyl K 100 Oracylic acid Phenolcarbinol Phenylcarboxy PHENYLCARBOXYLIC ACID Phenylformic acid Retarder BAX Retardex Tenn-Plas UCEPHAN Unisept BZA
Acide benzoïque ( Benzoic Acid)
BORIC ACID, N° CAS : 10043-35-3 / 11113-50-1 - Acide borique, Nom INCI : BORIC ACID, Nom chimique : Boric acid, N° EINECS/ELINCS : 233-139-2 / 234-343-4, acide borique borate d'hydrogène. ACIDE BORACIQUE; Acide borique; ACIDE ORTHOBORIQUE; BORON TRIHYDROXIDE; O-BORIC ACID; TRIHYDROXYDE DE BORE. Noms anglais :BORA ; BORACIC ACID; Borate compounds, Inorganic [10043-35-3], boric acid; Boric acid; HYDROGEN BORATE; ORTHOBORIC ACID. Utilisation: Agent ignifuge, fabrication de produits pharmaceutiques. BoratesSynonymes : acide boracique; acide orthoborique. Additif alimentaire : E284,Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes. Régulateur de pH : Stabilise le pH des cosmétiques. Dénaturant : Rend les cosmétiques désagréables. Principalement ajouté aux cosmétiques contenant de l'alcool éthylique.Ce solide blanc, parfois légèrement coloré, cristallise dans un réseau triclinique. Il se présente sous forme d'un solide cristallisé en paillettes nacrées. Assez peu soluble dans l'eau, c'est un acide faible à très faible. Il est souvent employé comme antiseptique bien que toxique, insecticide, absorbeur de neutrons dans les centrales nucléaires pour contrôler le taux de fission de l'uranium, et comme précurseur d'autres composés chimiques. Cet acide de Lewis tire son nom de l'un de ses composants, le bore, sa formule brute est H3BO3 ou en respectant mieux la structure à liaisons covalentes B(OH)3. L'acide borique moléculaire peut provenir de la simple décomposition du minéral naturel nommée sassolite qui, décrit par sa formule B(OH)3, n'est qu'un assemblage de plans d'acide borique stabilisés par des liaisons hydrogènes7. Il existe sous forme de cristaux incolores ou de poudre blanche se dissolvant dans l'eau. L'acide libre est présent sous forme native ou régénérée dans certaines zones possédant des batholithes granitiques proches de la surface telles que la Toscane, les îles Lipari et au Nevada, ses effluents sont mélangés à la vapeur issue des fissures de la croûte terrestre. En Toscane, on récupère l'acide borique dans des jets de vapeur d'eau surchauffée (100 à 215 °C) d'origine volcanique, exploités comme source d'énergie ; la vapeur, hydrolysant des borates dans les profondeurs du sol de cette région, contient en effet de l'acide borique et divers sels minéraux. Celle qui s'échappe librement des fissures du sol (soffioni) est simplement condensée dans des bassins (lagoni). La présence de l'acide borique ou de ses sels a été décelée dans l’eau de mer, et existerait également dans les végétaux et plus particulièrement dans presque tous les fruits8 où il pourrait jouer un certain rôle d'insecticide naturel. Disposition spatiale de molécules (hélicoïdales) d'acide borique dans son cristal artificiel ou dans la sassolite naturelle L'acide borique est le produit de dégradation ultime (souvent à l'aide d'un acide fort) de nombreux borates : borax, boracite, boronatrocalcite, colemanite, borocalcite, ascharite, kaliborite, kernite, kurnakovite, pinnaïte, pandermite, tunellite, larderellite, probertite, inderite, hydroboracite, etc., mais aussi howlite et bakérite, en plus des minéraux qui peuvent contenir l'acide borique en partie comme la harkérite ou la sassolite.L'acide borique est produit principalement à partir de minerai de borate par sa réaction avec l’acide sulfurique. La plus grande source de borates dans le monde est une mine à ciel ouvert située à Boron.En agriculture L'acide borique et ses sels sont utilisés comme fertilisants en agriculture conventionnelle et biologique14. La carence en bore est la carence en oligoéléments la plus répandue dans le monde et occasionne des pertes de rendement importantes chez les plantes cultivées et les arbres fruitiers15. En médecine et biologie Antiseptique Il peut être utilisé comme antiseptique pour les brûlures ou les coupures et est parfois employé dans les pommades et les onguents ou est utilisé dans une solution très diluée comme bain oculaire (eau boriquée). Comme composé anti-bactérien, l'acide borique peut également être prescrit comme traitement de l’acné. On l'utilise encore comme antiseptique pour l'oreille en plongée scaphandre, à raison d'une goutte d'alcool boriqué à 2 % par oreille.[réf. nécessaire] Le borate de sodium, un antiseptique doux, associé à d’autres composants appropriés peut également être proposé en usage externe pour des maladies des yeux, telle que la sécheresse oculaire. Antimycosique L'acide borique peut être utilisé pour traiter les levures et les mycoses comme les candidoses (mycoses vaginales) en remplissant de poudre d'acide borique des ovules qui seront insérés dans la cavité vaginale au coucher pendant trois à quatre nuits consécutives. en solution il peut être prescrit pour traiter certaines formes d’otites externes (infection de l'oreille) chez l’homme ou l’animal. Le conservateur dans les flacons d'urine (bouchon rouge) au Royaume-Uni est de l’acide borique. Il est également employé en prévention du pied d'athlète, en insérant la poudre dans les chaussettes ou les bas. Solution tampon Le borate de lithium est le sel de lithium de l'acide borique employé en laboratoire comme solution tampon pour le gel couramment employé dans les tampons d'électrophorèse des acides nucléiques (tels que les tampons TBE, SB et LB). Il peut être utilisé pour l’électrophorèse de l'ADN et de l'ARN, en gel de polyacrylamide et en gel d'agarose. Insecticide L'acide borique est également souvent utilisé comme insecticide relativement peu toxique, pour l’extermination des cancrelats, termites, fourmis, puces, et beaucoup d'autres insectes. Il peut être employé directement sous la forme de poudre pour les puces et les cancrelats, ou être mélangé avec du sucre ou de la gelée pour les fourmis. C'est également un composant de beaucoup d’insecticides du commerce. Dans cette utilisation, particulièrement dans le cas des cancrelats, l'acide borique sous forme de poudre est appliqué dans les zones fréquentées par les insectes. Les fines particules s'accrochent aux pattes des insectes et causent par la suite des brûlures chimiques mortelles. L'acide borique est commercialisé pour cet usage dans des quartiers résidentiels dans des zones urbaines infestées par les cancrelats. Esters of boric acid Octaborates Salts of boric acid Trioctyldodecyl borate Translated names Acid boric (ro) Acide borique (fr) Acido borico (it) Aċidu boriku (mt) Boorhape (et) Boorihappo (fi) Boorzuur (nl) Boric acid (no) Borna kiselina (hr) Boro rūgštis (lt) Borova kislina (sl) Borskābe (lv) Borsyra (sv) Borsyre (da) Borsäure (de) Bórsav (hu) Kwas borowy (pl) Kyselina boritá (cs) Kyselina trihydrogenboritá (sk) Ácido bórico (es) Βορικό οξύ (el) Борна киселина (bg) Acidium boricum Boric acid (H3BO3) boric acid. Trihydroxidoboron Boric acidTrihydrooxidoboron boric acidTrihydroxidoboron Ortho-boric Acid Orthoboric Acid TRHIOSSOBORIC ACID Trihydroxidoboron s BORIC ACID 99,9% Optibor Optibor HG Optibor TG Optibor TP 10043-35-3 [RN] Acide borique [French] acidum boricum [Latin] B(OH)3 [Formula] Boric acid Boric acid-11B Borsäure [German] Orthoboric acid (10B)Orthoboric acid 7440-42-8 [RN] Acidum boricum Ant flip Boracic acid Boracic Acid, Orthoboric Acid Borate (H3bo3) borate ion Boric acid ACS grade Boric acid Electrophoresis grade Boric acid flakes Boric acid, biochemical grade Boric Acid, Granular Boric acid, NF/USP grade Boric Acid, Powder Boric acid-d3 BORIC-11B ACID Borofax Boron hydroxide Boron trihydroxide Borsaeure Borsaure H3-BO3 Heptaoxotetra-Borate(2-) Homberg's salt Hydrogen borate hydrogen orthoborate InChI=1S/BH3O3/c2-1(3)4/h2-4H Kill-off Kjel-sorb Orthboric acid Orthoboricacid Orthoborsaeure tetraborate trihydridoborate trihydroxidoboron Trihydroxyborane Trihydroxyborone WLN: QBQQ
Acide borique
CAPRIC ACID, N° CAS : 334-48-5, Nom INCI : CAPRIC ACID, Nom chimique : Decanoic acid, N° EINECS/ELINCS : 206-376-4, Agent nettoyant : Aide à garder une surface propre; Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile), Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit, Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation, Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques; Noms français : 1-NONANECARBOXYLIC ACID; Acide caprique; ACIDE CAPRIQUE NORMAL; ACIDE DECANOIQUE; ACIDE DECANOIQUE NORMAL;DECOIC ACID; DECYCLIC ACID; DECYLIC ACID; N-CAPRIC ACID; N-DECANOIC ACID; N-DECYLIC ACID. Noms anglais : Capric acid; CAPRINIC ACID; CAPRYNIC ACID; DECANOIC ACID; N-DECOIC ACID; Utilisation: Fabrication de produits organiques, additif alimentaire. Capric Acid; Capric acid (CAS 334-48-5); n-decanoic acid Translated names Acid decanoic (ro) Acide décanoïque (fr) Acido decanoico (it) Aċidu dekanojku (mt) Decaan-zuur (nl) Decanoic acid (no) Decansyre (da) Decansäure (de) Dekaanhape (et) Dekaanihappo (fi) Dekano rūgštis (lt) Dekanojska kislina (sl) Dekanová kyselina (cs) Dekanska kiselina (hr) Dekansyra (sv) Dekánsav (hu) Dekānskābe (lv) Kwas dekanowy (pl) Kyselina dekánová (sk) Ácido decanoico (es) Δεκανικό οξύ (el) Деканова киселина (bg) 1- Decansäure 2-Ethyl-7-sulfo-decansäure Deacnoic acid s Capric Acid – Palmata 1099 Ecoric 10/95 Ecoric 10/99 KORTACID (KORTACID 1099/ 1098/1095/1090) Kortacid 1098 MASCID 1098 Palmac 98-10 Palmac 99-10 Palmac 99-10/MB RADIACID 0610 RADIACID 0613 RADIACID 0691
Acide caprylique ( CAPRYLIC ACID)
CITRIC ACID, N° CAS : 77-92-9 / 5949-29-1 - Acide citrique, Origine(s) : Naturelle, Synthétique, Autres langues : Acido citrico, Zitronensäure, Ácido cítrico, Nom INCI : CITRIC ACID, Nom chimique : 2-Hydroxy-1,2,3-propanetricarboxylic acid, N° EINECS/ELINCS : 201-069-1, Additif alimentaire : E330. L'acide citrique est un des principaux actifs du citron. Il est souvent utilisé pour équilibrer le pH (trop basique) des produits cosmétiques. Il est aussi présent dans certains produits de bain (bombes de bain, galets de bain ou "poudres magiques") en raison de ses propriétés effervescentes.Ses fonctions (INCI). Régulateur de pH : Stabilise le pH des cosmétiques. Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit
Acide citrique ( CITRIC ACID)
DEHYDROACETIC ACID, N° CAS : 520-45-6 / 771-03-9 / 16807-48-0 - Acide déhydroacétique, Autres langues : Acido deidroacetico, Dehydroessigsäure, Ácido deshidroacético. Nom INCI : DEHYDROACETIC ACID, Nom chimique : 3-Acetyl-6-methyl-2H-pyran-2,4(3H)-dione, N° EINECS/ELINCS : 208-293-9 / 212-227-4 / - Additif alimentaire : E265. Classification : Règlementé, Conservateur. L'acide déhydroacétique est utilisé dans les cosmétiques en tant que conservateur pour ses actions de fongicide et bactéricide. Il est employé sous la dénomination E265 en alimentaire. Comme il est Biodégradable, ce produit chimique ne pose pas de problème pour l'environnement, et les risques pour la santé restent assez faible. Notez toutefois, que le composé est interdit dans les sprays de type aérosol. L'acide déhydroacétique est autorisé en Bio.Ses fonctions (INCI): Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Noms français : 3-ACETYL-4-HYDROXY-6-METHYL-2H-PYRAN-2-ONE 3-ACETYL-6-METHYL-2,4-PYRANDIONE 3-ACETYL-6-METHYLDIHYDROPYRANDIONE-2,4 3-ACETYL-6-METHYLPYRANDIONE-2,4 4-HEXENOIC ACID, 2-ACETYL-5-HYDROXY-3-OXO-, DELTA-LACTONE ACETYL-3 METHYL-6 PYRANDIONE-2,4 Acide déhydroacétique METHYLACETOPYRONONE Noms anglais : Dehydroacetic acid Utilisation: Fabrication de produits organiques, bactéricide
Acide déhydroacétique ( Dehydroacetic acid)
THIODIPROPIONIC ACID N° CAS : 111-17-1 - Acide thiodipropanoïque Nom INCI : THIODIPROPIONIC ACID Nom chimique : 3,3'-Thiodipropionic Acid N° EINECS/ELINCS : 203-841-3 Additif alimentaire : E388 Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état
Acide diphosphorique ( Acide thiodipropanoïque)
SACCHAROSONIC ACID; ISOASCORBIC ACID; ERYTHORBIC ACID; N° CAS : 89-65-6 - Acide érythorbique. Nom INCI : ERYTHORBIC ACID. Nom chimique : 2,3-Didehydro-D-erythro-hexono-1,4-lactone; D-erythro-hex-2-enonic acid, gamma-lactone. N° EINECS/ELINCS : 201-928-0. Additif alimentaire : E315. Ses fonctions (INCI). Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Noms français : ACIDE ARABOASCORBIQUE ACIDE D-ERYTHORBIQUE ACIDE D-ISOASCORBIQUE ACIDE ERYTHORBIQUE ACIDE GLUCOSACCHARONIQUE ACIDE ISOASCORBIQUE ACIDE SACCHAROSONIQUE D-ERYTHRO-3-KETOHEXONIC ACID LACTONE D-ERYTHRO-3-OXOHEXONIC ACID LACTONE D-ERYTHRO-ASCORBIC ACID D-ERYTHRO-HEX-2-ENONIC ACID GAMMA-LACTONE D-ERYTHRO-HEX-2-ENONIC ACID, GAMMA-LACTONE Noms anglais : ARABOASCORBIC ACID D-ARABOASCORBIC ACID D-ERYTHORBIC ACID D-ISOASCORBIC ACID ERYTHORBIC ACID GLUCOSACCHARONIC ACID ISOASCORBIC ACID SACCHAROSONIC ACID Utilisation et sources d'émission Agent anti-oxydant, agent de préservation alimentaire. (5R)-5-[(1R)-1,2-Dihydroxyethyl]-3,4-dihydroxy-2(5H)-furanon [German] (5R)-5-[(1R)-1,2-Dihydroxyethyl]-3,4-dihydroxy-2(5H)-furanone (5R)-5-[(1R)-1,2-Dihydroxyéthyl]-3,4-dihydroxy-2(5H)-furanone [French] (5R)-5-[(1R)-1,2-Dihydroxyethyl]-3,4-dihydroxyfuran-2(5H)-one 228-973-9 [EINECS] 2410 311332OII1 84271 [Beilstein] 89-65-6 [RN] D-(-)-Isoascorbic acid D-Araboascorbic Acid D-erythro-3-Ketohexonic acid lactone D-erythro-3-Oxohexonic acid lactone D-erythro-Hex-2-enoic acid γ-lactone D-erythro-Hex-2-enonic Acid g-Lactone D-erythro-Hex-2-enonic acid, γ-lactone D-Isoascorbic acid Erycorbin Erythorbic acid [Wiki] Glucosaccharonic acid KF3015000 Mercate "5" Mercate 5 MFCD00005378 [MDL number] Saccharosonic Acid (2R)-2-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one (5R)-5-(1,2-dihydroxyethyl)-3,4-dihydroxy-5-hydrofuran-2-one (5R)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxy-2,5-dihydrofuran-2-one (R)-5-((R)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one [89-65-6] 2,3-Didehydro-D-erythro-hexono-1,4-lactone 6381-77-7 [RN] Araboascorbic acid D-(-)-Araboascorbic acid D(-)-Isoascorbic acid d(-)-isoascorbic acid 98% d(-)-isoascorbic acid, 98% d-(-)-isoascorbic acid, 98% d-(-)-isoascorbicacid D-ARABOASCORBICACID D-Erythorbic acid D-ERYTHRO-HEX-2-ENONIC ACID γ-LACTONE D-erythro-hex-2-enono-1,4-lactone D-Isoascorbic acid|D-Erythorbic acid ISD ISOASCORBIC ACID Isovitamin C UNII:311332OII1 UNII-311332OII1
Acide érythorbique ( ISOASCORBIC ACID)
EDTA, N° CAS : 60-00-4 - Acide éthylène diamine tétraacétique. Nom INCI : EDTA. Nom chimique : 1,2-Ethanediamine, N,N,N',N'-tetrakis(carboxymethyl)-, N° EINECS/ELINCS : 200-449-4, Additif alimentaire : E385. Classification : EDTA. L'EDTA (EDTA et ses principaux sels utilisés en cosmétique Disodium EDTA, Tetrasodium EDTA, Trisodium EDTA) est un agent chélateur que l'on emploie depuis les années 30 et pour lequel les industriels maîtrisent totalement la transformation et l'usage. Sa principale propriété est de complexer les métaux lourds. C'est-à-dire qu'il va en quelque sorte les neutraliser en formant avec eux un complexe, pour leur servir ensuite de transporteur et les évacuer. Il est donc assez logiquement utilisé en médecine pour lutter contre les intoxications aux métaux lourds (au plomb par exemple). Il est souvent employé en tant que séquestrant (calcium, calcaire ...) dans les savons ou gels douches, cela permet notamment de gérer les eaux "dures".Ses fonctions (INCI). Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques. Noms français : (ETHYLENEDINITRILO) TETRAACETIC ACID (ETHYLENEDINITRILO)TETRAACETIC ACID 3,6-BIS(CARBOXYMETHYL)-3,5-DIAZOOCTANEDIOIC ACID 3,6-DIAZAOCTANEDIOIC ACID, 3,6-BIS(CARBOXYMETHYL)- ACETIC ACID, (ETHYLENEDINITRILO)TETRA- ACETIC ACID, 2,2',2'',2'''-(1,2-ETHANEDIYLDINITRILO)TETRAKIS- ACIDE ETHYLENEDIAMINETETRACETIQUE Acide édétique Acide éthylènediaminetétraacétique ETHYLEBISIMINODIACETIC ACID ETHYLENE BIS (IMINODIACETIC ACID) ETHYLENEDINITRILOTETRAACETIC ACID N,N'-1,2-ETHANEDIYLBIS(N-(CARBOXYMETHYL)GLYCINE) Noms anglais : E D T A E.D.T.A. EDTA EDTA (CHELATING AGENT) EDTA ACID ETHYLENE DIAMINE TETRAACETIC ACID ETHYLENEDIAMINE TETRAACETIC ACID ETHYLENEDIAMINE-N,N,N',N'-TETRAACETIC ACID Ethylenediaminetetraacetic acid GLYCINE, N,N'-1,2-ETHANEDIYLBIS(N-CARBOXYMETHYL)- Utilisation et sources d'émission Agent chélateur, agent de dosage analytique
Acide éthylène diamine tétraacétique ( EDTA)
EDTMP, N° CAS : 1429-50-1 - Acide éthylènediaminetétraméthylène phosphonique. Nom INCI : EDTMP. Ses fonctions (INCI), Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques
Acide éthylènediaminetétraméthylène phosphonique (EDTMP)
HYDROXYETHANEDIPHOSPHONIC ACID; HEDP; ETIDRONIC ACID, N° CAS : 2809-21-4 - Acide étidronique, Origine(s) : Synthétique , Nom INCI : ETIDRONIC ACID , Nom chimique : Phosphonic acid, (1-hydroxyethylidene)bis- , N° EINECS/ELINCS : 220-552-8. L'acide étidronique est utilisé en tant qu'agent chélateur dans les cosmétiques. Il crée des complexes avec le calcium, l'arsenic, le fer et autres ions métalliques pour les neutraliser. Cela permet de gérer l'utilisation d'eaux un peu "dures", qui pourraient interférer avec les tensioactifs du produit par exemple. Ses fonctions (INCI) Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques. oms français : (1-HYDROXYETHYLIDENE)BIS(PHOSPHONIC ACID) (1-HYDROXYETHYLIDENE)DIPHOSPHONIC ACID (HYDROXYETHYLIDENE)DIPHOSPHONIC ACID 1-HYDROXYETHANE-1,1-BIPHOSPHONIC ACID 1-HYDROXYETHANE-1,1-DIPHOSPHONIC ACID 1-HYDROXYETHANEDIPHOSPHONIC ACID 1-HYDROXYETHYLIDENE-1,1-DIPHOSPHONIC ACID ACIDE HYDROXY-1 ETHYLIDENE DIPHOSPHONIQUE-1,1 ACIDE HYDROXYETHYLIDENE DIPHOSPHONIQUE EHDP ETHANE-1-HYDROXY-1,1-DIPHOSPHONIC ACID HYDROXYETHANE-1,1-DIPHOSPHONIC ACID OXYETHYLIDENEDIPHOSPHONIC ACID PHOSPHONIC ACID, (1-HYDROXYETHYLIDENE)BIS- PHOSPHONIC ACID, (1-HYDROXYETHYLIDENE)BIS-, PHOSPHONIC ACID, (1-HYDROXYETHYLIDENE)DI-, Noms anglais : ETIDRONIC ACID HYDROXYETHANEDIPHOSPHONIC ACID Utilisation et sources d'émission Agent chélateur
Acide étidronique ( HEDP)
FUMARIC ACID, N° CAS : 110-17-8 - Acide fumarique, Nom INCI : FUMARIC ACID. Nom chimique : Fumaric acid. N° EINECS/ELINCS : 203-743-0. Additif alimentaire : E297. Ses fonctions (INCI). Régulateur de pH : Stabilise le pH des cosmétiques. Noms français : (E)-BUTENEDIOIC ACID 1,2-ETHYLENE DICARBOXYLIC ACID (E) 2-BUTENEDIOIC ACID (E)- 2-BUTENEDIOIC ACID, (E)- ACIDE BOLETIQUE ACIDE BUTENEDIOIQUE (TRANS-) Acide fumarique ACIDE LICHENIQUE BUTENEDIOIC ACID,(E)- TRANS-1,2-ETHYLENE DICARBOXYLIC ACID TRANS-1,2-ETHYLENEDICARBOXYLIC ACID TRANS-BUTENEDIOIC ACID Noms anglais : BOLETIC ACID Fumaric acid LICHENIC ACID Utilisation : Fabrication de résines. Fumaric acid [Wiki] (2E)-2-Butendisäure [German] (2E)-2-Butenedioic acid (2E)-But-2-enedioic acid (E)-1,2-Ethylenedicarboxylic acid (E)-2-Butenedioic acid (E)-Butenedioic acid 1,2-Ethenedicarboxylic acid, trans- 110-17-8 [RN] 203-743-0 [EINECS] 2-Butenedioic acid 2-Butenedioic acid (2E)- 2-Butenedioic acid, (2E)- [ACD/Index Name] 2-Butenedioic acid, (E)- 605763 [Beilstein] Acide (2E)-2-butènedioïque [French] Acidum fumaricum Butenedioic acid, (E)- E-2-Butenedioic acid MFCD00002700 [MDL number] trans-1,2-ethenedicarboxylic acid trans-1,2-ethylenedicarboxylic acid TRANS-2-BUTENEDIOIC ACID trans-but-2-enedioic acid trans-Butenedioic acid (2E)-But-2-enedioate (E)-2-Butenedioate (E)-but-2-enedioate (E)-but-2-enedioic acid (E)-HO2CCH=CHCO2H 1,2-Ethylenedicarboxylic acid, (E) 2-(E)-Butenedioate 2-(E)-Butenedioic acid 2-Butenedioic acid (E)- 4-02-00-02202 [Beilstein] 605762 [Beilstein] Allomaleate Allomaleic acid Allomalenic acid Boletate Boletic acid cis-Butenedioic acid Fumaricum acidum Fumarsaeure Kyselina fumarova [Czech] Lichenate Lichenic acid (VAN) QV1U1VQ-T [WLN] trans-1,2-Ethylenedicarboxylate trans-2-Butenedioate trans-Butenedioate 延胡索酸 [Chinese]
Acide fumarique ( Fumaric acid)
GLUCONIC ACID, N° CAS : 526-95-4 - Acide gluconique. Nom INCI : GLUCONIC ACID. Nom chimique : D-gluconic acid. N° EINECS/ELINCS : 208-401-4. Additif alimentaire : E574. Ses fonctions (INCI). Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques. Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. Noms français : Acide D-gluconique; Acide gluconique; D-GLUCONIC ACID; DEXTRONIC ACID; Gluconic acid; GLUCONIC ACID, D-GLYCOGENIC ACID; GLYCONIC ACID; MALTONIC ACID; PENTAHYDROXYCAPROIC ACID. Noms anglais : Gluconic acid. Utilisation: Additif alimentaire. D-Gluconic acid 1726055 [Beilstein] 2,3,4,5,6-Pentahydroxycaproic acid 208-401-4 [EINECS] 526-95-4 [RN] Acide D-gluconique [French] D-Gluconsäure [German] Gluconic acid Glyconic Acid 2,3,4,5,6-pentahydroxy-hexanoic acid Dextronate Glycogenate Glyconate Maltonate (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid (3S,2R,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid [526-95-4] 157663-13-3 [RN] 2,3,4,5,6-pentahydroxyhexanoate 2,3,4,5,6-Pentahydroxyhexanoic acid 2-dehydro-3-deoxy-D-gluconate 2-keto-3-deoxy-D-gluconate 50% aqueous solution 50% gluconic acid solution 9025-70-1 [RN] d-(+)-gluconic acid Dextranase Dextronic acid D-gluco-Hexonic acid D-Gluconic acid - 45-50% in water D-Gluconic Acid (50per cent in Water) D-Gluconic acid 50% in water D-Gluconsaeure D-GLUCOSONIC ACID D-Glukonsaeure d-葡萄糖酸溶液 Galactonic acid GCO Glosanto Gluconic Acid (contains Gluconolactone) Gluconic acid (VAN) GLUCONIC ACID, D- gluconicacid Glycogenic acid ketogluconic acid Maltonic acid Pentahydroxycaproate Pentahydroxycaproic acid UNII:R4R8J0Q44B UNII-R4R8J0Q44B 葡萄糖酸 [Chinese]
Acide gluconique ( Gluconic acid)
GLUTAMIC ACID, N° CAS : 56-86-0 - Acide glutamique. Origine(s) : Synthétique. Autres langues : Acido glutammico, Glutaminsäure, Ácido glutamico. Nom INCI : GLUTAMIC ACID. Nom chimique : (S)-2-Aminopentanedioic acid. N° EINECS/ELINCS : 200-293-7. Additif alimentaire : E620. Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau
Acide glutamique ( GLUCURONIC ACID)
GLUTARIC ACID, N° CAS : 110-94-1. Nom INCI : GLUTARIC ACID. Nom chimique : 1,3-Pentanedioic acid. N° EINECS/ELINCS : 203-817-2. Ses fonctions (INCI): Régulateur de pH : Stabilise le pH des cosmétiques. Noms français : 1,3-PROPANEDICARBOXYLIC ACID; 1,5-PENTANEDIOIC ACID; Acide glutarique; ACIDE PENTANEDIOIQUE; ACIDE PENTANEDIOIQUE-1,5; ACIDE PROPANEDICARBOXYLIQUE-1,3; Glutaric acid; PENTANEDIOIC ACID. Noms anglais : Glutaric acid. Utilisation: Fabrication de produits organiques. 1,3-Propanedicarboxylic acid. Glutaric acid ; 1,3-Propanedicarboxylate; 1,5-Pentanedioate; 1,5-Pentanedioic acid; 110-94-1 [RN]; 1209725 [Beilstein]; 203-817-2 [EINECS]; Acide glutarique [French] ; Glutarsäure hydrogen glutarate; MFCD00004410 [MDL number]; n-Pyrotartaric acid; Pentanedioic acid [ACD/Index Name]; 1,3-PROPANEDICARBOXYLIC ACID; 111-16-0 [RN]; 203-817-2MFCD00004410 271-678-5 [EINECS] 273-081-5 [EINECS] 4-02-00-01934 (Beilstein Handbook Reference) [Beilstein] 68603-87-2 [RN] 68937-69-9 [RN] 8065-59-6 [RN] Glutaric acid (Pentanedioic acid) glutaric acid, reagent Pentandioate Pentandioic acid pentanedioate Propane-1,3-dicarboxylic acid Propane-1,3-dicarboxylic acid|Pentanedioic acid,Glutaric acid WLN: QV3VQ 戊二酸 [Chinese] 1,5-Pentanedioic acid Glutaric acid n-Pyrotartaric acid Pentandioic acid CAS names Pentanedioic acid CH02923 Glutarsäure pentanedioic acid.
Acide glutarique ( GLUTARIC ACID)
Glycol acid; GLYCOLIC ACID; N° CAS : 79-14-1 - Acide glycolique, Origine(s) : Végétale, Synthétique. Nom INCI : GLYCOLIC ACID. Nom chimique : Acetic acid, hydroxy-, N° EINECS/ELINCS : 201-180-5, L'acide glycolique est un acide organique naturel, aussi nommé acides alpha-hydroxylés (AHA). Il est généralement fabriqué à partir de canne à sucre. Il est utilisé dans les peeling doux et produits exfoliants à base d'acide. Il permet d'accélérer la perte des cellules mortes et favorise le renouvellement cellulaire. Comme les autres acides de fruits, on l'emploie aussi pour lisser les rides, éclaircir le teint, estomper les tâches pigmentaires et les irrégularités de la peau.Ses fonctions (INCI): Régulateur de pH : Stabilise le pH des cosmétiques. Noms français : Acide glycolique; ACIDE; HYDROXYACETIQUE; HYDROXY ACETIC ACID; Hydroxyacetic acid; HYDROXYETHANOIC ACID. Noms anglais : Glycolic acid. Utilisation: Fabrication de produits textiles, fabrication de produits organiques. 1209322 [Beilstein]; 201-180-5 [EINECS]; 2-Hydroxyethanoic acid; 79-14-1 [RN]; Acetic acid, 2-hydroxy- [ACD/Index Name];Acide glycol [French] [ACD/IUPAC Name] Acide hydroxyacétique [French]; a-Hydroxyacetic acid; Glycol acid [ACD/IUPAC Name] Glycolic acid Glycolsäure [German] Hydroxyessigsäure [German] [ACD/IUPAC Name] Kyselina glykolova [Czech] Kyselina hydroxyoctova [Czech] QV1Q [WLN] 1,2-Ethanediol [ACD/Index Name] 102962-28-7 [RN] 1-hydroxy-ethanoic acid 26009-03-0 [RN] 2-oxonioacetate D-malate EDO GLV Glycocide Glycolic acid, 66-70% aqueous solution glycolic acid, crystal, reagent Glycolic acid, pure, 99.5% Glycollic acid Glyoxylic acid GOA HOCH2COOH Hydroxy-acetic acid Hydroxyethanoic acid Kyselina glykolova MFCD00868116 [MDL number] MLT TAR WLN: QV1Q α-Hydroxyacetic acid α-Hydroxyacetic acid 乙醇酸 [Chinese]. Acetic acid, 2-hydroxy- Acetic acid, hydroxy- Glycollic acid Hydroxyacetic acid Hydroxyethanoic acid Kyselina glykolova Kyselina hydroxyoctova Translated names Acid glicolic (ro) Acide glycolique (fr) Acido glicolico (it) Aċidu glikolliku (mt) Glikolio rūgštis (lt) Glikolna kiselina (hr) Glikolna kislina (sl) Glikolsav (hu) Glikolskābe (lv) Glycolic acid (no) glycolsyre (da) Glycolzuur (nl) Glykolihappo (fi) glykolová kyselina/2-hydroxyethanová kyselina (cs) Glykolsyra (sv) Glykolsäure (de) Glükoolhape (et) Kwas glikolowy (pl) kyselina glykolová (sk) Ácido glicólico (es) Γλυκολικό οξύ (el) Гликолова киселина (bg) 2-hydroxy acetic acid 2-Hydroxyacetic acid 2-Hydroxyethanoic acid glycol acid Glykolsäure ... %
Acide glycolique ( Glycolic acid )
Cas : 67701-05-7, EC : 266-929-0, Fatty acids, C8-18 and C18-unsatd.
Acide gras de coco
hyaluronan, HYALURONIC ACID, N° CAS : 9004-61-9 - Acide hyaluronique,Autres langues : Acido ialuronico, Hyaluronsäure, Ácido hialurónico, Nom INCI : HYALURONIC ACID, Nom chimique : Hyaluronic acid. N° EINECS/ELINCS : 232-678-0. Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau. Hydratant : Augmente la teneur en eau de la peau et aide à la maintenir douce et lisse. Agent d'entretien de la peau : Maintient la peau en bon état
Acide hyaluronique
HYDROLYZED HYALURONIC ACID, Acide hyaluronique hydrolysé, Nom INCI : HYDROLYZED HYALURONIC ACID. Ses fonctions (INCI) : Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau. Agent d'entretien de la peau : Maintient la peau en bon état
Acide hyaluronique hydrolysé ( HYDROLYZED HYALURONIC ACID)
ARACHIDIC ACID, Icosa-5,8,11,14-tetraenoic acid; N° CAS : 506-30-9 - Acide icosanoïque ou acide arachidique, Nom INCI : ARACHIDIC ACID, Nom chimique : Icosanoic acid, N° EINECS/ELINCS : 208-031-3. Noms français :Acide arachidique; ACIDE EICOSANOIQUE; EICOSANOIC ACID. Noms anglais : ARACHIC ACID; Arachidic acid; Utilisation: Produit organique, Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Opacifiant : Réduit la transparence ou la translucidité des cosmétiques. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. 208-031-3 [EINECS] 506-30-9 [RN] Acide icosanoïque [French] ácido n-eicosanoico [Spanish] Arachic acid Arachidic acid Arachidinic acid Arachinsaeure [German] Eicosanoic acid Icosanoic acid Icosansäure [German] 5,8,11-Eicosatriynoic Acid|5,8,11-eicosatriynoic acid ACD arachidic acid, 98% Arachidic acid;Eicosanoic acid Arachidic Acid|eicosanoic acid ARACHIDIC ACID|ICOSANOIC ACID arachidicacid Arachinsaeure Eicosanic acid Eicosanoic acid (Arachidic acid) eicosanoic acid, 99% Eicosanoicacid Eicosatetraynoic Acid|5,8,11,14-eicosatetraynoic acid ethyl stearic acid icosanoicacid
Acide icosanoïque ou acide arachidique ( Arachidic acid )
maleicacid; Maleinic acid; Malenic acid; Maleic acid; MALEINIC ACID; MALENIC ACID; TOXILIC ACID; ACIDE MALEINIQUE; ACIDE MALENIQUE; Acide maléique; acide (Z)-but-2-èn-1,4-dioïque, acide Z-butènedioïque, acide maléique, No CAS: 110-16-7, Nom INCI : MALEIC ACID.ácido maleico; Allomaleic acid; Allomalenic acid ;Nom chimique : 2-Butenedioic acid (2Z)-. N° EINECS/ELINCS : 203-742-5. Ses fonctions (INCI) : Régulateur de pH : Stabilise le pH des cosmétiques. L'acide maléique est un acide dicarboxylique insaturé, l'acide Z-butènedioïque. Cette molécule est le diastéréoisomère de l'acide fumarique ou acide E-butènedioïque, la configuration montre que les groupements carboxyles, caractéristiques des acides organiques sont placés sur un plan du même côté de la liaison éthylénique, c'est-à-dire de la double liaison carbone-carbone, rigide. Les sels de ses anions et les esters sont appelés maléates.Noms français : (Z)-BUTEDIOIC ACID; 1,2-ETHYLENEDICARBOXYLIC ACID, (Z); 2-BUTENEDIOIC ACID (Z)-; ACIDE BUTENEDIOIQUE (CIS-); ACIDE MALEINIQUE; ACIDE MALENIQUE; Acide maléique; CIS-1,2-ETHYLENEDICARBOXYLIC ACID; CIS-BUTENEDIOIC ACID.Noms anglais : Maleic acid; MALEINIC ACID; MALENIC ACID; TOXILIC ACID. Utilisation : Fabrication de produits organiques et de résines; Maleic acid; (2Z)-2-Butendisäure [German] [ACD/IUPAC Name]; (2Z)-2-Butenedioic acid [ACD/IUPAC Name]; (2Z)-But-2-enedioic acid; 110-16-7 [RN]; 2-Butenedioic acid, (2Z)- [ACD/Index Name]; 605762 [Beilstein]; Acide (2Z)-2-butènedioïque [French] [ACD/IUPAC Name]; Acidum maleicum; cis-Butenedioic acid; toxilic acid; trans-but-2-enedioic acid; (2Z)-But-2-ene-1,4-dioic acid; (2Z)-but-2-enedioate; (2Z)but-2-enedioic acid; (2Z)-Butene-2-dioate; (2Z)-Butene-2-dioic acid; (Z)-1,2-Ethenedicarboxylic Acid; (Z)-2-butenedioate; (Z)-2-Butenedioic acid; (Z)-but-2-enedioic acid; (z)-butenedioate; (Z)-butenedioic acid; 1,2-dihydropyridazine-3,6-dione; 1,2-Ethylenedicarboxylic acid, (Z); 1,2-Ethylenedicarboxylic acid, cis-; 2-Butenedioic acid [ACD/IUPAC Name]; 2-Butenedioic acid (2Z)-; 2-Butenedioic acid (Z)-; 2-Butenedioic acid, (Z)-; ácido maleico; Allomaleic acid; Allomalenic acid; Boletic acid; but-2-enedioic acid; BUTENE-1,4-DIOIC ACID; Butenedioic acid; Butenedioic acid, (Z)-; Butenedioic acid,(Z)-; cis-1,2-ethylenedicarboxylic acid; cis-2-Butenedioate; CIS-2-BUTENEDIOIC ACID; cis-But-2-enedioate; cis-but-2-enedioic acid; Cis-butenedioate; Fumaric acid; H2male; hydrogen maleate; Kyselina maleinova [Czech];Kyselina maleinova; Lichenic acid; MAE; maleic acid reference material; Maleic acid|(2Z)-But-2-ene-1,4-dioic acid; maleic acid-cp; maleicacid; Maleinic acid; Malenic acid; Malezid CM;polymaleic acid; QV1U1VQ-C [WLN]; ZEELCHEM 200;Z-fumaric acid; 馬來酸 [Chinese]; (Z)-but-2-enová kyselina (cs); acid maleic (ro); acide maléique (fr); acido maleico (it); aċidu malejku (mt); kwas maleinowy (pl); kyselina maleínová (sk); Maleiinhape (et); maleiinihappo (fi); maleino rūgštis (lt); maleinová kyselina (cs); maleinsav (hu); maleinska kiselina (hr); maleinska kislina (sl); maleinsyra (sv); maleinsyre (da); Maleinsäure (de); maleïnezuur (nl); maleīnskābe (lv); ácido maleico (es); μηλεϊνικό οξύ (el); малеинова киселина (bg); CAS names: 2-Butenedioic acid (2Z)-; : (2Z)-but-2-enedioic acid; (Z)-But-2-enedioic acid; (Z)-Butenedioic acid; (Z)-Butenedioic acid, Maleic acid; but-2-enedioic acid; but-2-enedioic acid ; cis-1,2-Ethylendicarbonsäure; cis-Butendisäure; cis-Butenedioic acid, Toxilic acid, Acidum maleicum, Butenedioic Acid; Maleic acid (Z)-Butenedioic acid; Maleinsaeure; Maleinsäurelösung; MEXORYL SCO; Trade names: 2-Butenedioic acid (Z)- (9CI); 2-Butenedioic acid, (Z)-; cis-1,2-Ethylenedicarboxylic acid; cis-2-Butenedioic acid; cis-Butenedioic acid; Maleic acid (40% in water); Maleic acid (8CI); Toxilic acid
Acide maléique ( maleic acid )
MERCAPTOPROPIONIC ACID, N° CAS : 107-96-0, Nom INCI : MERCAPTOPROPIONIC ACID. Nom chimique : 3-Mercaptopropionic acid, N° EINECS/ELINCS : 203-537-0. Dépilatoire : Enlève les poils indésirables. Agent bouclant ou lissant (coiffant) : Modifie la structure chimique des cheveux, pour les coiffer dans le style requis. Agent réducteur : Modifie la nature chimique d'une autre substance en ajoutant de l'hydrogène ou en éliminant l'oxygène.beta.-Mercaptopropionic acid.beta.-Thiopropionic acid, 2-Mercaptoethanecarboxylic acid, 3-MERCAPTOPROPANOIC ACID, 3-MERCAPTOPROPIONATE, 3-mercaptopropionic acid, 3-sulfanylpropanoic acid, 3-thiohydracrylic acid, 3-Thiolpropanoic acid, 3-Thiopropanoic acid, 3-THIOPROPIONIC ACID, 3MPA, beta-Mercaptopropanoic acid, beta-Mercaptopropionate. BETA-MERCAPTOPROPIONIC ACID. BETA-THIOPROPIONIC ACID. EINECS 203-537-0. Hydracrylic acid, 3-thio-, Propanoic acid, 3-mercapto- Propanoic acid, 3-mercapto-, coco alkyl esters, Propionic acid, 3-mercapto-, PROPIONIC ACID, 3-MERCPATO-, Propionic acid, mercapto-, USAF E-5
Acide mercaptopropionique
FORMIC ACID, N° CAS : 64-18-6 - Acide méthanoïque ou Acide Formique, Nom INCI : FORMIC ACID, Nom chimique : Formic acid, N° EINECS/ELINCS : 200-579-1; Additif alimentaire : E236. Noms français : Acide formique; ACIDE METHANOIQUE; HYDROGEN CARBOXYLIC ACID; METHANOIC ACID. Noms anglais : AMINIC ACID; Formic acid; FORMYLIC ACID Utilisation: L'acide formique est utilisée notamment : en tant que préservatif pour la nourriture et pour l'ensilage;comme antiseptique dans le brassage;en tant qu'acidulant pour teindre les fibres naturelles et synthétiques; dans le tannage du cuir; pour coaguler le latex dans la production de caoutchouc;comme plastifiant dans certaines résines;en tant que réactif en chimie organique dans la manufacture de fumigants et d'insecticides. 1209246 [Beilstein]; 213-057-3 [EINECS]; 213-129-4 [EINECS]; 231-791-2 [EINECS]; 64-18-6 [RN];Acide formique [French] Acido formico [Italian] Ameisensäure [German] Formic acid [ACD/Index Name] [Wiki] HCOOH [Formula] hydroxidooxidocarbon(.) Kwas metaniowy [Polish] Kyselina mravenci [Czech] Methanoic acid Mierenzuur [Dutch] β-Lactic acid 107-31-3 [RN] 147173-07-7 [RN] 1901013 [Beilstein] 2564-86-5 [RN] 2-trans-indole-3-butyryl-CoA 2-trans-indole-3-butyryl-Coenzyme A 3-hydroxy-indole-3-butyryl-CoA 3-hydroxy-indole-3-butyryl-coenzyme A 3-keto-indole-3-butyryl-CoA 3-keto-indole-3-butyryl-coenzyme A 6'-hydroxyferuloyl-CoA 7056-83-9 [RN] 8006-93-7 [RN] Acetate ion Acetic acid [ACD/Index Name] [Wiki] Add-F Amasil Ameisensaeure [German] Bilorin Carbon dioxide [JP15] [USAN] [USP] [Wiki] CBX Citric acid [Wiki] Collo-bueglatt Collo-didax FMT Formic acid anhydrous Formic Acid, ACS Grade Formic acid-d [ACD/Index Name] Formira Formisoton Formylic acid HOCO(.) http://www.hmdb.ca/metabolites/HMDB0000142 hydrocarboxyl radical Hydrogen carboxylic acid Hydrogencarboxylic acid Hydroxycarbonyl indole-3-acetyl-CoA indole-3-butyryl-CoA Kwas metaniowy Kyselina mravenci Methanol [ACD/Index Name] [Wiki] methoic acid METHOXY, OXO- MFCD00167028 [MDL number] Mierenzuur MOH MONOCARBOXYLIC ACID Myrmicyl Salachlor SEC65 protein Sybest TBF tert-Butyl formate
Acide palmitique
Acide oléique – 6,7,8 – polyglycolester, Inci : PEG-6 oleate, PEG-4 oleate, PEG-5 oleate, PEG-7 oleate; Cas : 9004-96-0; Oleic acid, ethoxylated; Oleic acid, 12EO; Poly(ethylene glycol) monooleate; Poly(oxy-1,2-ethanediyl), .alpha.-(1-oxo-9-octadecenyl)-.omega.- hydroxy-, (Z)-
Acide polyglycolester
PROPIONIC ACID, N° CAS : 79-09-4 - Acide propanoïque. Nom INCI : PROPIONIC ACID. Nom chimique : Propionic acid. N° EINECS/ELINCS : 201-176-3. Additif alimentaire : E280, Classification : Règlementé, Conservateur. Compatible Bio (Référentiel COSMOS). Ses fonctions (INCI) : Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Noms français : Acide propanoïque; Acide propionique. Noms anglais : Carboxyethane; Ethanecarboxylic acid; Ethylformic acid; Metacetonic acid; Methyl acetic acid; Propanoic acid; Propionic acid; Pseudoacetic acid. Utilisation et sources d'émission: Fabrication de produits organiques et pharmaceutiques; Noms français : Acide propanoïque; Acide propionique. Noms anglais : Carboxyethane ; Ethanecarboxylic acid; Ethylformic acid; Metacetonic acid; Methyl acetic acid; Propanoic acid; Propionic acid; Pseudoacetic acid; Utilisation et sources d'émission: Fabrication de produits organiques et pharmaceutiques. Antischim B; C3 acid; Carboxyethane; Ethanecarboxylic acid; Ethylformic acid; Kyselina propionova; Luprosil; Metacetonic acid; Methyl acetic acid; Monoprop; Propionic acid (natural); propionic acid ... %; Propionic acid grain preserver; PROPIONIC ACID ; propionic acid ; Prozoin; Pseudoacetic acid; Sentry grain preserver; Tenox P grain preservative . Translated names: propiono rūgštis (lt); Acid propionic (ro); acid propionic … % (ro); Acide propionique (fr); acide propionique ... % (fr); Acido propionico (it); acido propionico ... % (it); Aċidu propjoniku (mt); kwas etanokarboksylowy ...% (pl); kwas metylooctowy ...% (pl); Kwas propionowy (pl); kwas propionowy ...% (pl); Kyselina propionová (cs); Kyselina propiónová (sk); Propano rūgštis (lt); propansyra ... % (sv); Propionic acid (no); Propionihappo (fi); Propionihappo... % (fi); propionová kyselina ...% (cs);Propionsav (hu); propionsav …% (hu); Propionska kiselina (hr); propionska kiselina ... % (hr); Propionska kislina (sl); propionska kislina...% (sl); Propionskābe (lv); Propionsyra (sv); propionsyra ... % (sv); Propionsyre (da); propionsyre ... % (da); Propionsäure (de); Propionsäure ... % (de); Propionzuur (nl); propionzuur ... % (nl); Propioonhape (et); Propioonhape … % (et); propánová kyselina ... % (sk); Ácido propiónico (es); ácido propiónico ... % (es); Προπιονικό οξύ (el); προπιονικό οξύ ... % (el); Пропионова киселина (bg); пропионова киселина... % (bg); % propionskābe (lv). CAS names: Propanoic acid. : Acid C3, Propanoic acid, Propanyl acid, Methyl acetic acid; n-Propionic Acid; propionic acid...%. Trade names: Adofeed; Carboxylic acid c3; E 280; Fema number 2924; Methylacetic acid; N-propanoic acid; Propanoic acid (9CI); Propcorn; Propionic acid (6CI, 8CI); Propionsaeure; Propkorn
Acide propanoïque ( Propionic acid)
STEARIC ACID, N° CAS : 57-11-4 - Acide stéarique, Origine(s) : Végétale, Animale, Synthétique,Autres langues : Acido stearico, Stearinsäure, Ácido esteárico. Nom INCI : STEARIC ACID, Nom chimique : Stearic acid, N° EINECS/ELINCS : 200-313-4, Additif alimentaire : E570. Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre; Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Stabilisateur d'émulsion : Favorise le processus d'émulsification et améliore la stabilité et la durée de conservation de l'émulsion. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Agent de restauration lipidique : Restaure les lipides des cheveux ou des couches supérieures de la peau Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation; Noms français : Acide octadécanoïque ; Acide stéarique. Noms anglais :1-Heptadecane carboxylic acid; 1-Heptadecanecarboxylic acid; Octadecanoic acid; Stearic acid. Utilisation et sources d'émission: Fabrication de produits pharmaceutiques et de savons; Stearic acid EC Inventory, , , EU. Com. Reg. No 10/2011 on plastic materials in contact with food CAS names : Octadecanoic acid. IUPAC names; acide octadécanoïque; Stearic acid (even numbered); Stearic Acid C18; stearic acid; Octadecanoic acid
Acide stéarique ( Acide octadécanoïque )
SUCCINIC ACID, N° CAS : 110-15-6 - Acide succinique, Nom INCI : SUCCINIC ACID, Nom chimique : Butanedioic acid, N° EINECS/ELINCS : 203-740-4.Additif alimentaire : E363. Compatible Bio ; Ses fonctions (INCI). Régulateur de pH : Stabilise le pH des cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit; Noms français : 1,2-ETHANE DICARBOXYLIC ACID; 1,2-ETHANEDICARBOXYLIC ACID; 1,4-BUTANEDIOIC ACID; ACIDE BUTANEDIOIQUE-1,4; Acide succinique; BUTANEDIOIC ACID; DIHYDROFUMARIC ACID; ETHYLENE DICARBOXYLIC ACID. Noms anglais : Succinic acid. Utilisation et sources d'émission : Fabrication de laques, fabrication de colorants; 1,2-Ethanedicarboxylic acid; 1,4-Butanedioic acid ; Acidum succinicum; Amber acid; Asuccin; Bernsteinsaure; Butandisaeure; Dihydrofumaric acid; Ethylene dicarboxylic acid; Ethylenesuccinic acid; Katasuccin; Kyselina jantarova Succinate ; Succinic acid; Succinicum acidum; Wormwood acid. CAS names: Butanedioic acid. IUPAC names : Butanedionic acid; Ethanedicarboxylic acid; Succinic; 1,2-Ethanedicarboxylic acid ; 1,4-Butanedioic acid; 110-15-6 [RN]; 203-740-4 [EINECS]; 4-02-00-01908 [Beilstein]; Acide butanedioique [French]; Acide succinique [French] ; Acido succinico [Italian]; ácido succínico [Spanish]; Ácido succínico [Portuguese]; acidum succinicum [Latin]; Bernsteinsaeure [German]; Bernsteinsäure [German] ; Butanedioic acid ; HOOC-CH2-CH2-COOH [Formula]; Kyselina jantarova [Czech]; MFCD00002789 [MDL number]; Succinic acid ; Succinic acid; Ηλεκτρικό οξύ ; Янтарная кислота [Russian]; コハク酸 [Japanese]; 琥珀酸 [Chinese]; acidum succinicum amber acid; asuccin; Bernsteinsaeure; Bernsteinsaure; Butandisaeure; BUTANE DIACID; BUTANEDIOICACID; Dihydrofumaric acid; Ethanedicarboxylic acid; Ethylene dicarboxylic acid ; Ethylene succinic acid; FMR; fum; Fumaric acid ; Katasuccin; Kyselina jantarova; Sal succini; Succinellite; succinic acid(free acid); succunic acide; Wormwood acid
Acide succinique ( succinic acid ) Butanedioic acid
L'acide sulfonique est un acide hypothétique de formule chimique HSO2OH. C'est un tautomère instable de l'acide sulfureux HO-SO-OH. C'est un composé instable qui présente peu d'intérêt en tant que tel, mais il existe de nombreux composés stables en dérivant, de formules chimiques R-SO2OH, pour lesquelles le groupement fonctionnel -SO2OH est appelé fonction acide sulfonique, le composé dans son ensemble étant appelé de manière générale un acide sulfonique.
Acide sulfonique pur
TARTARIC ACID, N° CAS : 133-37-9 / 147-71-7 / 87-69-4 - Acide tartrique. Autres langues : Acido tartarico, Weinsäure, Ácido tartárico. Nom INCI : TARTARIC ACID. Nom chimique : 2,3-Dihydroxybutanedioic acid, N° EINECS/ELINCS : 205-105-7 / 205-695-6 / 201-766-0. Additif alimentaire : E334. Compatible Bio (Référentiel COSMOS). Ses fonctions (INCI). Régulateur de pH : Stabilise le pH des cosmétiques. Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit; Noms français : (+-)-Acide tartarique; (+-)-Acide tartrique; Acide dihydroxy-2,3 ; butanedioïque; Acide DL-tartarique; Acide DL-tartrique; Acide paratartarique; Acide tartarique; Acide tartarique (DL-); Acide tartarique racémique. Acide tartrique. Noms anglais : (+-)-Tartaric acid ; 2,3-Dihydroxybutanedioic acid; DL-Tartaric acid; Paratartaric acid; Racemic acid; Racemic tartaric acid; Resolvable tartaric acid; Tartaric acid; Tartaric acid, (+-)-; Uvic acid; Utilisation et sources d'émission : Fabrication de produits de tannage, additif alimentaire; (±)-tartaric acid. IUPAC names : (+-)-Tartaric acid; (2R,3R)-2,3-dihydroxybutanedioic acid ; 2, 3-Dihydroxybutanedioic Acid; 2,3 dihydroxybutanedioic acid; 2,3-Dihydroxybutanedioic acid; 2,3-dihydroxysuccinic acid; Acide Tartrique Poudre; Butanedioic acid, 2,3-dihydroxy-, (2R,3R)-rel-; DL-Tartaric Acid; Tartaric acid; L-(+)-Tartaric acid; (+)-(2R,3R)-Tartaric acid; (+)-(R,R)-tartaric acid; (+)-L-tartaric acid; (+)-tartaric acid; (2R,3R)-(+)-Tartaric acid; (2R,3R)-2,3-Dihydroxybernsteinsäure [German] [ACD/IUPAC Name]; (2R,3R)-2,3-dihydroxybutanedioic acid; (2R,3R)-2,3-Dihydroxysuccinic acid [ACD/IUPAC Name]; (2R,3R)-tartaric acid (R,R)-(+)-tartaric acid; (R,R)-tartaric acid; [R-(R*,R*)]-2,3-Dihydroxybutanedioic Acid; 133-37-9 [RN]; 1725147 [Beilstein]; 201-766-0 [EINECS]; 205-105-7 [EINECS]; 87-69-4 [RN]; Acide (2R,3R)-2,3-dihydroxysuccinique [French] [ACD/IUPAC Name]; Acidum tartaricum; Butanedioic acid, 2,3-dihydroxy-, (2R,3R)- [ACD/Index Name]; Butanedioic acid, 2,3-dihydroxy-, (2R,3R)-rel- ; L-(+)-Tartarate; L-(+)-Tartrate; L-2,3-Dihydroxybutanedioic Acid; L-tartaric acid; L-threaric acid; MFCD00064207 [MDL number]; Ordinary Tartaric Acid; Tartarate [ACD/IUPAC Name] Tartaric acid [ACD/IUPAC Name] ; Weinsaure [German]; Weinsteinsaure [German]; (+)-tartarate; (2R,3R)-Tartarate; (R,R)-tartarate;(R,R)-tartrate; 2,3-dihydroxybutanedioate; 2,3-dihydroxy-succinate; 2,3-dihydroxysuccinic acid; 2,3-Dihydroxy-succinic acid; L-tartarate; tartrate ; Weinsaeure; (+)-Weinsaeure; (1R,2R)-1,2-Dihydroxyethane-1,2-dicarboxylic acid; (2R,3R)-(+)-2,3-Dihydroxybutane-1,4-dioic acid, (2R,3R)-(+)-2,3-Dihydroxysuccinic acid; (2R,3R)-2,3-Dihydroxybernsteinsaeure ;(2R,3R)-2,3-dihydroxybutanedioate (2R,3R)-2,3-tartaric acid (2R,3R)-rel-2,3-Dihydroxybutanedioic acid (2R,3R)-rel-2,3-Dihydroxysuccinic acid (R,R)-(+)-tartatic acid 1,2-DIHYDROXYETHANE-1,2-DICARBOXYLIC ACID 138508-61-9 [RN] 144814-09-5 [RN] 147-71-7 [RN] 2,3-dihydrosuccinic acid 2,3-dihydroxybutanedioic acid 205-695-6 [EINECS] 39469-81-3 [RN] 3-hydroxymalic acid 4231301 [Beilstein] 526-83-0 [RN] 526-83-087-69-4 56959-20-7 [RN] 69-72-7 [RN] ACS D(-)-TARTARIC ACID D-(-)-Tartaric Acid (en) Dl-dihydroxysuccinic acid hydrogen (2R,3R)-tartrate l-​(+)​-​tartaric acid l-( )-tartaric acid L-(+) tartaric acid L(+)-Tartaric acid L-(+)-Tartaric acid, ACS l-(+)-tartaric acid, anhydrous L(+)-Tartaricacid L-(+)-Tartaricacid lamB protein (fungal) l-tartaricacid l-酒石酸 Metatartaric acid MFCD00071626 [MDL number] R,R-tartaric acid Rechtsweinsaeure TAR Tartaric acid (TN) THREARIC ACID TLA Weinsteinsaeure
Acide tartrique ( TARTARIC ACID)
MYRISTIC ACID, N° CAS : 544-63-8 - Acide tétradécanoïque (Acide myristique), Acide tetradécanoïque .Synonymes : 1-TRIDECANECARBOXYLIC ACID;ACIDO MYNISTICO;Butter acids;Coconut oil fatty acids;CRODACID;EMERY 655;HYDROFOL ACID 1495;Hystrene 9014;Myristic acid, pure;Myristinsaeure;N-TETRADECAN-1-OIC ACID;N-TETRADECANOIC ACID;N-TETRADECOIC ACID;neo-Fat 14;TETRADECANSAEURE;UNIVOL U 316S.Nom INCI : MYRISTIC ACID. Nom chimique : Tetradecanoic acid. N° EINECS/ELINCS : 208-875-2. Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. Noms français : 1-TRIDECANECARBOXYLIC ACID; Acide myristique; ACIDE TETRADECANOIQUE; ACIDE TETRADECANOIQUE NORMAL; ACIDE TETRADECANOIQUE-1; N-TETRADECAN-1-OIC ACID; N-TETRADECANOIC ACID; N-TETRADECOIC ACID; NORMAL-TETRADECANOIC ACID. Noms anglais :Myristic acid; TETRADECANOIC ACID. Utilisation et sources d'émission: Fabrication de parfums et de savons. 1-tetradecanoic acid; 1-Tridecanecarboxylic acid; 208-875-2 [EINECS]; 508624 [Beilstein]; 544-63-8 [RN];Acide myristique [French] [ACD/IUPAC Name]; Acide tétradécanoïque [French]; myristic acid [ACD/IUPAC Name]; Myristinsäure [German] [ACD/IUPAC Name]; n-Myristic acid; n-TETRADECANOIC ACID; Tetradecanoic acid [ACD/Index Name]; 1-Tridecanecarboxylate; n-Tetradecan-1-oaten-Tetradecanoate; 1,2-DIMYRISTOYL-RAC-GLYCERO-3-PHOSPHOCHOLINE; 12-O-Tetradecanoylphorbol 13-acetate; 12-Tetradecanoylphorbol 13-acetate; 13-Tetradecynoic acid [ACD/Index Name] [ACD/IUPAC Name]; 1-tetradecanecarboxylate; 1-tetradecanecarboxylic acid; 4-02-00-01126 [Beilstein]; 82909-47-5 [RN]; Crodacid; Methyl 11-methyldodecanoate [ACD/IUPAC Name]; Myristic Acid 655; Myristinsaeure; Myristoate; Myristoic acid; n-Tetradecan-1-oic acid; n-tetradecoate; n-Tetradecoic acid; QV13 [WLN]; tetradecanoate; TetradecanoicAcid; tetradecoate; tetradecoic acid
Acide tétradécanoïque (Acide myristique)
mercaptoacetic acid; Acide thioglycolique; 2-MERCAPTOACETIC ACID; THIOGLYCOLIC ACID, N° CAS : 68-11-1 - Acide thioglycolique et ses sels, Nom INCI : THIOGLYCOLIC ACID, Nom chimique : Mercaptoacetic acid, N° EINECS/ELINCS : 200-677-4; Classification : Règlementé. L'acide thioglycolique modifie les fibres des cheveux pour faciliter leur restructuration : on l'utilise par exemple dans les produits restructurant capillaires. On l'emploie aussi pour décomposer chimiquement les poils indésirables pour qu'ils puissent ensuite être éliminés en les essuyant simplement. C'est son sel de potassium qui est le plus utilisé aujourd'hui.Ses fonctions (INCI). Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Dépilatoire : Enlève les poils indésirables. Agent bouclant ou lissant (coiffant) : Modifie la structure chimique des cheveux, pour les coiffer dans le style requis. Agent réducteur : Modifie la nature chimique d'une autre substance en ajoutant de l'hydrogène ou en éliminant l'oxygène. Noms français : 2-MERCAPTOACETIC ACID; 2-MERCAPTOETHANOIC ACID; 2-THIOGLYCOLIC ACID; ACIDE MERCAPTO-2 ACETIQUE; ACIDE MERCAPTO-2 ETHANOIQUE; ACIDE MERCAPTOACETIQUE; ACIDE THIO-2 GLYCOLIQUE; Acide thioglycolique; ALPHA-MERCAPTOACETIC ACID; MERCAPTOACETIC ACID; Noms anglais : ACETIC ACID, MERCAPTO-; Thioglycolic acid; THIOGLYCOLLIC ACID; THIOVANIC ACID. Utilisation: L'acide thioglycolique est un produit utilisé dans une grande variété d'applications, dont les cosmétiques, la fabrication des plastiques et la chimie analytique. Il est utilisé notamment: en coiffure pour l'ondulation permanente des cheveux; en tant qu'ingrédient dans des produits capillaires; pour faire des produits dépilatoires; dans certains produits pharmaceutiques; pour faire des thioglycolates utilisés dans l'industrie du plastique (emballages, additifs pour le PVC); pour modifier la laine ou le cuir; en chimie analytique pour différents procédés (par exemple la séparation de l'aluminium du fer); 2-Mercaptoacetate; 2-Mercaptoacetic acid; 2-Thioglycolic acid; Acetic acid, 2-mercapto-; Acetic acid, mercapto-; Glycolic acid, 2-thio-; Glycolic acid, thio-; Kyselina merkaptooctova; Kyselina thioglykolova; Mercaptoacetic acid; Mercaptoessigsaeure; Salts of Thioglycolic acid; Thioglycolate; THIOGLYCOLIC ACID; Thioglycollic acid; Thiovanic acid. Translated names: acid tioglicolic (ro); acide mercaptoacétique (fr); acide thioglycolique (fr); acido tioglicolico (it); kwas 2-sulfanylooctowy (pl); kwas merkaptooctowy (pl); kwas tioglikolowy (pl); kyselina tioglykolová (sk); mercaptoeddikesyre (da); merkaptoacto rūgštis (lt); merkaptoeddiksyre (no); merkaptoättiksyra (sv); thioglycolsyre (da); thioglycolzuur (nl); thioglykolová kyselina (cs); Thioglykolsäure (de); kiselina (hr); tioglikolna kislina (sl);tioglikolsav, merkaptoecetsav (hu); tioglikolskābe (lv); Tioglykolihappo (fi); tioglykolsyra (sv); tioglykolsyre (no); Tioglükoolhape (et); ácido mercaptoacético (es); ácido tioglicólico (es); θειογλυκολικό οξύ (el); тиогликолова киселина (bg).IUPAC names: 2-Sulfanylacetic acid; sulfanylacetic acid; Thioglycolic acid TGA, mercaptoacetic acid; THIOGLYKOLSAEURE. Trade names : Thio Glycolic Acid; Thioglycolic Acid 70%, technical grade; Thioglycolic Acid 80%, cosmetic grade; Thioglycolic Acid 80%, cosmetic grade, low odor; Thioglycolic Acid 80%, pure; Thioglycolic Acid 80%, technical grade; Thioglycolic Acid 85% cosmetic grade; Thioglycolic Acid 85%, technical grade; Thioglycolic Acid 97%, technical grade; Thioglycolic Acid 98%; Thioglycolic Acid 98%, commercial grade; Thioglycolic Acid 99% pure; Thioglycolic Acid 99%, cosmetic grade, low odor; Thioglycolic Acid 99%,cosmetic grade; 200-677-4 [EINECS]; 2-Mercaptoacetic acid; 2-mercaptoethanoic acid; 2-thioglycolic acid; 506166 [Beilstein]; 68-11-1 [RN]; Acetic acid, 2-mercapto- [ACD/Index Name]; acetic acid, mercapto-; acetyl mercaptan; Acide sulfanylacétique [French] ;Acide thioglycolique [French]; Glycolic acid, 2-thio-; Glycolic acid, thio-; Kyselina merkaptooctová [Czech]; Kyselina thioglykolová [Czech]; mercaptoacetic acid; Mercaptoessigsaeure [German]; mercaptoethanoic acid; Merkaptoessigsaeure [German]; MFCD00004876 [MDL number]; Sulfanylacetic acid [ACD/IUPAC Name]; Sulfanylessigsäure [German] ;Thioglycolic acid; thioglycolic acid; thioglycollic acid; Thioglykolsaeure [German]; α-mercaptoacetic acid; 2-sulfanylacetic acid; 2-sulfanylethanoic acid; Acetic acid; Acide thioglycolique; Acide thioglycolique [French]; Kyselina merkaptooctova [Czech]; Kyselina thioglykolova [Czech]; mercapto acetic acid; METHYLTHIO, CARBOXY-; SH1VQ [WLN]; sJPhLPDIKTp@; Thioglycolicacid; Thiovanic acid; WLN: SH1VQ; α-mercaptoacetic acid; α-Mercaptoacetic acid; 巯基乙酸 [Chinese]
Acide thioglycolique et ses sels ( THIOGLYCOLIC ACID) acide thioglycolique ( mercaptoacetic acid )
EC / List no.: 287-494-3; CAS no.: 85536-14-7; Mol. formula: C19H32O3S; Acide Linear alkyl benzène sulfonique ( labsa ) Linear alkyl benzène acide sulfonique est un grand tensioactif synthétique de volume en raison de son coût relativement faible , de bonnes performances , le fait qu'il peut être séché pour obtenir une poudre stable et le respect de l'environnement biodégradable. 2-Dodecylbenzenesulfonic acid; 4-(tridecan-3-yl)benzene-1-sulfonic acid; 4-Alkylbenzenesulfonic acid; Alkylbenzene C10-C13 sec , sulfonation product with sulphur trioxide; Benzenesulfonic acid; Benzenesulfonic acid, 4-C1-13-sec-alkyl derivs.; Benzenesulfonic Acid, 4-C10-13-Sec-Alkyl Derivatives; Benzenesulfonic acid, 4-C10-13-sec-alkyl derivs; Benzenesulfonic acid, 4-C10-13-sec-alkyl derivs..; Benzenesulfonic acid, 4-C10-13-sec-alkyl derivs.H; Benzesulfonic acid, 4-C10-13-sec-alkyl derivs.; Dodecylbenzene sulfonic acid, mixture of C10-C13 isomers; Dodecylbenzene sulphonic acid; LAB sulpohonic acid, Alkylbenzene sulfonic acid; LABSA; LABSA (Linear Alkylbenzene Sulphonic Acid); Linear alkyl benzene sulfonic acid; Linear Alkyl benzene Sulphonic acid; Linear alkylbenzene sulfonate; Linear Alkylbenzene Sulfonic Acid; Linear alkylbenzene sulphonic acid; Linear alkylbenzenesulphonic acid
Acide Linear alkyl benzène sulfonique
COCONUT ACID N° CAS : 61788-47-4 - Acides gras de coco Origine(s) : Végétale Autres langues : Acidi grassi di cocco, Coconut fatty acids, Kokosfettsäuren, Ácidos grasos de coco Nom INCI : COCONUT ACID N° EINECS/ELINCS : 262-978-7 Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre Emollient : Adoucit et assouplit la peau Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. MIXED COCONUT FATTY ACIDS Noms anglais : COCONUT OIL FATTY ACIDS FATTY ACIDS, COCO FATTY ACIDS, COCONUT OIL