N,N-Dimethyl-N-ethanolamine is colorless or slightly yellow liquid with ammonia odor.
N,N-Dimethyl-N-ethanolamine has a role as a curing agent and a radical scavenger.
N,N-Dimethyl-N-ethanolamine is a tertiary amine and a member of ethanolamines.

CAS Number: 108-01-0
Molecular Formula: C4H11NO
Molecular Weight: 89.14
EINECS Number: 203-542-8

2-(Dimethylamino)ethanol, Deanol, N,N-Dimethylethanolamine, 108-01-0, Dimethylethanolamine, Dimethylaminoethanol, 2-DIMETHYLAMINOETHANOL, Norcholine, DMAE, Bimanol, Liparon, Varesal, N,N-Dimethylaminoethanol, Propamine A, DMEA, Ethanol, 2-(dimethylamino)-, (2-Hydroxyethyl)dimethylamine, Kalpur P, Dimethylmonoethanolamine, Dimethylaminoaethanol, N,N-Dimethyl-2-hydroxyethylamine, Amietol M 21, N,N-Dimethyl-2-aminoethanol, N-Dimethylaminoethanol, Texacat DME, N,N-Dimethyl ethanolamine, 2-(N,N-Dimethylamino)ethanol, Dimethyl(hydroxyethyl)amine, Dimethylaethanolamin, Dimethyl(2-hydroxyethyl)amine, 2-(Dimethylamino)-1-ethanol, N-(2-Hydroxyethyl)dimethylamine, Demanol, Demanyl, N,N-Dimethyl-N-(2-hydroxyethyl)amine, (Dimethylamino)ethanol, beta-Hydroxyethyldimethylamine, beta-Dimethylaminoethyl alcohol, 2-(Dimethylamino) ethanol, 2-Dwumetyloaminoetanolu, 2-Dimethylamino-ethanol, N,N-Dimethyl-N-(beta-hydroxyethyl)amine, NSC 2652, CCRIS 4802, N-(Dimethylamino)ethanol, Oristar dmae, HSDB 1329, N,N-Dimethyl(2-hydroxyethyl)amine, Tegoamin DMEA, EINECS 203-542-8, Dabco DMEA, UNII-2N6K9DRA24, 2-(dimethylamino)ethan-1-ol, Deanol [BAN], BRN 1209235, 2N6K9DRA24, DIMETHYL MEA, AI3-09209, CHEBI:271436, NSC-2652, N,N'-Dimethylethanolamine, 2-(dimethylamino)-ethanol, (CH3)2NCH2CH2OH, CHEMBL1135, .beta.-(Dimethylamino)ethanol, .beta.-Hydroxyethyldimethylamine, .beta.-Dimethylaminoethyl alcohol, DTXSID2020505, NSC2652, EC 203-542-8, Phosphatidyl-N-dimethylethanolamine, Deanol (BAN), MFCD00002846, n-(2-hydroxyethyl)-n,n-dimethylamine, N,N-DIMETHYLAMINOETHANOL (DMAE), NCGC00159413-02, Tonibral, N,N-Dimethyl-N-(.beta.-hydroxyethyl)amine, DEANOL (MART.), DEANOL [MART.], DTXCID00505, rexolin, CAS-108-01-0, Dimethylaethanolamin [German], Dimethylamino ethanol, Dimethylaminoaethanol [German], 2-Dwumetyloaminoetanolu [Polish], 2-Dimethylamino ethanol, UN2051, Ethanol, 2-dimethylamino-, N,N-Dimethyl-N-ethanolamine, 2-dimethylamino, N,N Dimethyl 2 hydroxyethylamine, Jeffcat DMEA, Dimethylethanoiamine, Toyocat -DMA, dimethyl ethanolamine, dimethyl-ethanolamine, DIMETHOL, Paresan (Salt/Mix), dimethyl ethanol amine, THANCAT DME, 2-dimethyamino-ethanol, n,n-dimethylethanolamin, Biocoline (Salt/Mix), beta-dimethylaminoethanol, N,N dimethylaminoethanol, DEANOL [WHO-DD], DEANOL [MI], N,N-dimethyl-ethanolamine, N,N-dimethylamino ethanol, N,N-dimethylethanol amine, N,N-dimethylethanol-amine, (n,n-dimethylamino)ethanol, 2-Hydroxyethyldimethylamine, 2-Dimethylaminoethanol [UN2051] [Corrosive], beta-(Dimethylamino)ethanol, beta -(dimethylamino)ethanol, DIMETHYL MEA [INCI], Dimethylaminoaethanol(german), N,N-Dimethylethanolamine (2-Dimethylaminoethanol), Choline chloride (Salt/Mix), Luridin chloride (Salt/Mix), beta -hydroxyethyldimethylamine, N,N-Dimethylethanolamine/DMEA, beta -dimethylaminoethyl alcohol, DMAE1549, 2-(N,N-dimethyl amino)ethanol, 2-(N,N-dimethylamino) ethanol, N-hydroxyethyl-N,N-dimethylamine, 2-(N,N-dimethyl amino) ethanol, beta -(dimethylamino)ethyl alcohol, 2-hydroxy-N,N-dimethylethanaminium, B-DIMETHYLAMINOETHYL ALCOHOL, WLN: Q2N1 & 1, 2-Dimethylaminoethanol, >=99.5%, BCP22017, CS-M3462, N,N-Dimethyl-beta-hydroxyethylamine, .beta.-(Dimethylamino)ethyl alcohol, N, N-Dimethyl(2-hydroxyethyl)amine, Tox21_113163, Tox21_201821, Tox21_302844, BDBM50060526, N,N-Dimethyl-beta -hydroxyethylamine, N,N-Dimethylaminoethanol, redistilled, 2-(DIMETHYLAMINO)ETHYL ALCOHOL, AKOS000118738, N,N-Dimethyl-.beta.-hydroxyethylamine, DB13352, N,N-DIMETHYLETHANOLAMINE [HSDB], RP10040, UN 2051, N, N-Dimethyl-N-(2-hydroxyethyl)amine, NCGC00159413-03, NCGC00256454-01, NCGC00259370-01, BP-13447, N,N-Dimethyl-N-(beta -hydroxyethyl)amine, N, N-Dimethyl-N-(beta -hydroxyethyl)amine, D0649, NS00001173, D07777, DIMETHYLAMINOETHANOL, (CORROSIVE LIQUID), 2-Dimethylaminoethanol [UN2051] [Corrosive

N,N-Dimethyl-N-ethanolamine is an organic compound with the formula (CH3)2NCH2CH2OH.
The synthesis of N,N-Dimethyl-N-ethanolamine by the ethylene oxide method is obtained by the ammonification of dimethylamine with ethylene oxide, which is distilled, refined and dehydrated.
N,N-Dimethyl-N-ethanolamine has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.

In addition, in vivo experiments showed that N,N-Dimethyl-N-ethanolamine is not methylated to choline and does not alter brain ACh levels.
Interestingly, in both acute and chronic seizure models in rats, a conjugate of N,N-Dimethyl-N-ethanolamine and valproate (DEVA) was shown to be more potent than valproate alone, potentially by facilitation of valproate transport via the blood brain barrier.
N,N-Dimethyl-N-ethanolamine is commonly referred to as 2-(dimethylamino)ethanol, dimethylaminoethanol (DMAE) or dimethylethanolamine (DMEA).

N,N-Dimethyl-N-ethanolamine holds tertiary amine and primary alcohol groups as functional groups.
N,N-Dimethyl-N-ethanolamine has been used in the treatment of attention deficit-hyperactivity disorder (ADHD), Alzheimer's disease, autism, and tardive dyskinesia.
However, results of several studies were inconclusive and a systematic review could not confirm the positive effects of N,N-Dimethyl-N-ethanolamine or other cholinergic compounds in patients with TD.

N,N-Dimethyl-N-ethanolamine is commonly referred to as 2-(dimethylamino)ethanol, dimethylaminoethanol (DMAE) or dimethylethanolamine (DMEA).
N,N-Dimethyl-N-ethanolamine holds tertiary amine and primary alcohol groups as functional groups.
N,N-Dimethyl-N-ethanolamine has been used in the treatment of attention deficit-hyperactivity disorder (ADHD), Alzheimer's disease, autism, and tardive dyskinesia.

N,N-Dimethyl-N-ethanolamine has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.
N,N-Dimethyl-N-ethanolamine and comes with molecular formula of C4H11NO and molecular weight of 89.13624.
N,N-Dimethyl-N-ethanolamine works as anti-depressive agent and is also used for treating movement disorders.

Available in colorless liquid form, it has amine odor with boiling point of 135 DEG C 758 MM HG, melting point of -59 DEG C, density/specific gravity of 0.8866 @ 20 DEG C/4 DEG C.
The chemical has miscible solubility with water, ether, acetone & benzene.
N,N-Dimethyl-N-ethanolamine is a tertiary amine that is ethanolamine having two N-methyl substituents.

N,N-Dimethyl-N-ethanolamine has a role as a curing agent and a radical scavenger.
N,N-Dimethyl-N-ethanolamine is a tertiary amine and a member of ethanolamines.
N,N-Dimethyl-N-ethanolamine is commonly referred to as 2-(dimethylamino)ethanol, dimethylaminoethanol (DMAE) or dimethylethanolamine (DMEA).

N,N-Dimethyl-N-ethanolamine holds tertiary amine and primary alcohol groups as functional groups.
N,N-Dimethyl-N-ethanolamine has been used in the treatment of attention deficit-hyperactivity disorder (ADHD), Alzheimer's disease, autism, and tardive dyskinesia.
N,N-Dimethyl-N-ethanolamine has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.

N,N-Dimethyl-N-ethanolamine is bifunctional, containing both a tertiary amine and primary alcohol functional groups.
N,N-Dimethyl-N-ethanolamine is a colorless viscous liquid.
N,N-Dimethyl-N-ethanolamine is used in skin care products for improving skin tone and also taken orally as a nootropic.

N,N-Dimethyl-N-ethanolamine is prepared by the ethoxylation of dimethylamine.
N,N-Dimethyl-N-ethanolamine, commonly known as Deanol, is a chemical compound with the molecular formula C4H11NO.
N,N-Dimethyl-N-ethanolamine is an organic compound that belongs to the class of alkanolamines.

N,N-Dimethyl-N-ethanolamine is a tertiary amine and has two methyl groups attached to the nitrogen atom, along with an ethyl group attached to the carbon adjacent to the nitrogen.
N,N-Dimethyl-N-ethanolamine is used as a curing agent for polyurethanes and epoxy resins.
N,N-Dimethyl-N-ethanolamine is a precursor to other chemicals, such as the nitrogen mustard 2-dimethylaminoethyl chloride.

The acrylate ester, N,N-Dimethyl-N-ethanolamine acrylate is used as a flocculating agent.
Related compounds are used in gas purification, e.g. removal of hydrogen sulfide from sour gas streams.
N,N-Dimethyl-N-ethanolamine is an organic chemical compound from the group of alkylated amino alcohols .

N,N-Dimethyl-N-ethanolamine is closely related to the neurotransmitter acetylcholine via choline (the trimethylethanolammonium cation).
N,N-Dimethyl-N-ethanolamine is an intermediate product of the chemical and pharmaceutical industries .
N,N-Dimethyl-N-ethanolamine is miscible with water, ethanol, benzene, ether and acetone.

N,N-Dimethyl-N-ethanolamine is a white powder providing 37% DMAE.
Animal tests show possible benefit for improving spatial memory and working memory.
N,N-Dimethyl-N-ethanolamine is produced industrially by reacting dimethylamine with ethylene oxide at temperatures of 125-160 ° C and pressures of 15-30 bar in the presence of catalytic amounts of water in liquid-cooled double-jacket tube reactors.

N,N-Dimethyl-N-ethanolamine is an organic compound with the formula (CH3)2NCH2CH2OH.
N,N-Dimethyl-N-ethanolamine is bifunctional, containing both a tertiary amine and primary alcohol functional groups.
N,N-Dimethyl-N-ethanolamine is a colorless viscous liquid.

N,N-Dimethyl-N-ethanolamine is used in skin care products for improving skin tone and also taken orally as a nootropic.
N,N-Dimethyl-N-ethanolamine is prepared by the ethoxylation of dimethylamine.
N,N-Dimethyl-N-ethanolamine is an amino alcohol.

N,N-Dimethyl-N-ethanolamine is the main product formed during the amination of ethylene glycol by dimethylamine on alumina supported copper in a continuous fixed-bed reactor.
N,N-Dimethyl-N-ethanolamine has been reported to be the putative precursor of acetylcholine.
N,N-Dimethyl-N-ethanolamine is effect as a skin-firming and anti-wrinkle agent has been studied.

Microwave spectrum of N,N-Dimethyl-N-ethanolamine has been investigated.
N,N-Dimethyl-N-ethanolamine is effect as an organic additive on deposition and anti-reflective properties of porous CaF2 has been studied.
Removal of the benzyl ester groups by transesterification with N,N-Dimethyl-N-ethanolamine from benzyl protected tripeptides has been reported.

N,N-Dimethyl-N-ethanolamine is a transparent, pale yellow liquid and primary alcohol that is used as a building block for the synthesis of cationic flocculants and ion exchange resins.
N,N-Dimethyl-N-ethanolamine is also used used as a chemical intermediate for pharmaceuticals, dyes, corrosion inhibitors, and emulsifiers and as an additive to boiler water, paint removers, and amino resins.
N,N-Dimethyl-N-ethanolamine is an organic compound with the formula (CH3)2NCH2CH2OH.

N,N-Dimethyl-N-ethanolamine is bifunctional, containing both a tertiary amine and primary alcohol functional groups.
N,N-Dimethyl-N-ethanolamine is a colorless viscous liquid.
N,N-Dimethyl-N-ethanolamine is used in skin care products.

N,N-Dimethyl-N-ethanolamine is prepared by the ethoxylation of dimethylamine.
N,N-Dimethyl-N-ethanolamine is a precursor to other chemicals, such as the nitrogen mustard 2-dimethylaminoethyl chloride.
The acrylate ester is used as a flocculating agent.Related compounds are used in gas purification, e.g. removal of hydrogen sulfide from sour gas streams.

N,N-Dimethyl-N-ethanolamine is a white powder providing 37% DMAE.
Deanol is commonly referred to as 2-(dimethylamino)ethanol, N,N-Dimethyl-N-ethanolamine or dimethylethanolamine (DMEA).
N,N-Dimethyl-N-ethanolamine holds tertiary amine and primary alcohol groups as functional groups.

N,N-Dimethyl-N-ethanolamine has been used in the treatment of attention deficithyperactivity disorder (ADHD), Alzheimer's disease, autism, and tardive dyskinesia.
N,N-Dimethyl-N-ethanolamine has been also used as an ingredient in skin care, and in cognitive function- and mood-enhancing products.
N,N-Dimethyl-N-ethanolamine appears as a clear colorless liquid with a fishlike odor.

N,N-Dimethyl-N-ethanolamine is a tertiary amine that is ethanolamine having two N-methyl substituents.
N,N-Dimethyl-N-ethanolamine has a role as a curing agent and a radical scavenger.
N,N-Dimethyl-N-ethanolamine is a tertiary amine and a member of ethanolamines.

N,N-Dimethyl-N-ethanolamine is a compound that many people believe can positively affect mood, enhance memory, and improve brain function.
N,N-Dimethyl-N-ethanolamine’s also thought to have benefits for aging skin.
While there aren’t many studies on N,N-Dimethyl-N-ethanolamine, advocates believe it may have benefits for several conditions, including: attention deficit hyperactivity disorder (ADHD).

N,N-Dimethyl-N-ethanolamine is naturally produced in the body.
N,N-Dimethyl-N-ethanolamine’s also found in fatty fish, such as salmon, sardines, and anchovies.
N,N-Dimethyl-N-ethanolamine is thought to work by increasing production of acetylcholine (Ach), a neurotransmitter that’s crucial for helping nerve cells send signals.

Ach helps regulate many functions controlled by the brain, including REM sleep, muscle contractions, and pain responses.
N,N-Dimethyl-N-ethanolamine may also help prevent the buildup of a substance called beta-amyloid in the brain.
Too much beta-amyloid has been linked to age-related decline and memory loss.

N,N-Dimethyl-N-ethanolamine’s impact on Ach production and beta-amyloid buildup may make it beneficial for brain health, especially as age.
N,N-Dimethyl-N-ethanolamine can be synthesized through the reaction of dimethylamine with ethylene oxide.
This reaction results in the formation of a tertiary amine, where two methyl groups are attached to the nitrogen atom and an ethyl group is attached to the adjacent carbon.

N,N-Dimethyl-N-ethanolamine finds various industrial applications due to its properties as a versatile amine.
N,N-Dimethyl-N-ethanolamine is commonly used as a catalyst or a reactant in chemical reactions, particularly in the synthesis of pharmaceuticals, pesticides, and corrosion inhibitors.
In cosmetics and personal care products, N,N-Dimethyl-N-ethanolamine is utilized as an ingredient in formulations such as skin care products, hair care products, and toiletries.

N,N-Dimethyl-N-ethanolamine can act as a pH adjuster, emulsifier, or conditioning agent in these formulations.
N,N-Dimethyl-N-ethanolamine has gained attention in the field of nootropics and cognitive enhancement.
Some individuals use Deanol-containing supplements for its potential to improve cognitive function, memory, and focus.

However, scientific evidence supporting these claims is limited, and more research is needed to determine its effectiveness and safety for cognitive enhancement purposes.
N,N-Dimethyl-N-ethanolamine is regulated by various regulatory bodies, including the U.S. Food and Drug Administration (FDA) and the European Chemicals Agency (ECHA).
N,N-Dimethyl-N-ethanolamine is important to adhere to regulations and guidelines regarding its use in different applications to ensure safety and compliance.

While Deanol is generally regarded as safe when used in accordance with regulations and guidelines, it is essential to handle it with care due to its potential hazards.
Proper safety precautions, such as wearing appropriate personal protective equipment and following handling instructions, should be observed when working with this compound.
Research on N,N-Dimethyl-N-ethanolamine continues to explore its potential applications and properties. Studies may focus on its chemical reactivity, biological effects, and
potential uses in various industries, contributing to ongoing advancements in science and technology.

N,N-Dimethyl-N-ethanolamine has previously been investigated as a stimulant and treatment for several neurological diseases, including tardive dyskinesia (TD), Alzheimer’s disease (AD) and senile dementia.
First, application of N,N-Dimethyl-N-ethanolamine to human healthy volunteers dates back to the 1960s when N,N-Dimethyl-N-ethanolamine was reported to exert stimulating effects comparable to amphetamine.
Murphree et al. (1960) described improved concentration, increased muscle tone and changed sleeping habits in healthy males (21–26 years) with an intake of 10–20 mg N,N-

Dimethyl-N-ethanolamine (or Deanol) daily for 2–3 weeks compared to a placebo group.
In later studies, N,N-Dimethyl-N-ethanolamine was hypothesized as an acetylcholine (ACh) precursor and therefore tested in diseases that are considered to be linked to the cholinergic system.
N,N-Dimethyl-N-ethanolamine is a tertiary amine that is ethanolamine having two N-methyl substituents.

Melting point: −70 °C(lit.)
Boiling point: 134-136 °C(lit.)
Density: 0.886 g/mL at 20 °C(lit.)
vapor density: 3.03 (vs air)
vapor pressure: 100 mm Hg ( 55 °C)
refractive index: n20/D 1.4294(lit.)
Flash point: 105 °F
storage temp.: Store below +30°C.
solubility: alcohol: miscible(lit.)
form: Liquid
pka: pK1:9.26(+1) (25°C)
color: Clear colorless to pale yellow
Odor: Amine like
PH Range: 10.5 - 11.0 at 100 g/l at 20 °C
PH: 10.5-11 (100g/l, H2O, 20℃)
explosive limit 1.4-12.2%(V)
Water Solubility: miscible
FreezingPoint: -59.0℃
Sensitive: Hygroscopic
Merck: 14,2843
BRN: 1209235
Stability: Stable. Flammable. Incompatible with oxidizing agents, copper, copper alloys, zinc, acids, galvanised iron. Hygroscopic.
InChIKey: UEEJHVSXFDXPFK-UHFFFAOYSA-N
LogP: -0.55 at 23℃

N,N-Dimethyl-N-ethanolamine is an aminoalcohol.
N,N-Dimethyl-N-ethanolamine has been submitted to the National Cancer Institute (NCI) for testing and evaluation and the Cancer Chemotherapy National Service Center (NSC) number is 2652.
N,N-Dimethyl-N-ethanolamine is sometimes included as an ingredient in combination products, alongside other compounds purported to have cognitive-enhancing effects.

These products may contain vitamins, minerals, antioxidants, or herbal extracts, aiming to synergistically improve cognitive function.
However, the efficacy of such combinations should be evaluated through rigorous scientific research.
N,N-Dimethyl-N-ethanolamine-containing products marketed for cognitive enhancement often attract public interest, particularly among individuals seeking ways to support brain health and cognitive performance.

N,N-Dimethyl-N-ethanolamine is important for consumers to critically evaluate marketing claims and seek evidence-based information from reliable sources when considering the use of these products.
Regulatory agencies oversee the safety and labeling of N,N-Dimethyl-N-ethanolamine-containing products to ensure compliance with regulations.
Manufacturers are responsible for conducting safety assessments, adhering to labeling requirements, and providing accurate information to consumers.

Regulatory oversight helps safeguard public health and prevent misleading claims or unsafe practices in the marketplace.
Educational resources, such as scientific literature, reputable websites, and healthcare professionals, can provide valuable information about N,N-Dimethyl-N-ethanolamine and its potential effects.
Consumers and healthcare providers can use these resources to make informed decisions about its use, weighing potential benefits against risks and considering individual health
needs and preferences.

N,N-Dimethyl-N-ethanolamine belongs to the ontological category of tertiary amine in the ChEBI Ontology tree.
The United Nations designated GHS hazard class pictogram is Flammable;Corrosive;Irritant, and the GHS signal word is DangerThe storage condition is described as Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
N,N-Dimethyl-N-ethanolamine use and application categories indicated by third-party sources: Fire Hazards -> Corrosives, Flammable - 2nd degree.

However, this does not mean N,N-Dimethyl-N-ethanolamine can be used or applied in the same or a similar way.
N,N-Dimethyl-N-ethanolamine has been studied for its potential biological effects, including its interaction with neurotransmitter systems in the brain.
Some research suggests that it may modulate levels of acetylcholine, a neurotransmitter involved in memory and cognition.

However, the exact mechanisms of action and their significance in cognitive function are still not fully understood.
Upon ingestion, N,N-Dimethyl-N-ethanolamine is metabolized in the body.
N,N-Dimethyl-N-ethanolamine undergoes processes such as oxidation and conjugation, leading to the formation of various metabolites.

Understanding its metabolic pathways is important for assessing its safety and potential health effects.
While N,N-Dimethyl-N-ethanolamine is generally considered safe when used appropriately, excessive intake or exposure may lead to adverse effects.
Some reported side effects include gastrointestinal disturbances, such as nausea and stomach upset.

Additionally, there have been concerns about potential liver toxicity associated with high doses, although more research is needed to confirm these effects.
N,N-Dimethyl-N-ethanolamine may interact with other substances, medications, or supplements.
Individuals taking medications or supplements should consult healthcare professionals before using N,N-Dimethyl-N-ethanolamine-containing products to avoid potential interactions or adverse effects.

N,N-Dimethyl-N-ethanolamine is available in various formulations, including oral supplements, topical creams, and liquid solutions.
The concentration and form of N,N-Dimethyl-N-ethanolamine in these products may vary, influencing its absorption, bioavailability, and effectiveness.
Despite its potential benefits, research on Deanol faces challenges, including variability in study designs, inconsistent findings, and a lack of standardized protocols.

Addressing these challenges is essential for advancing scientific understanding and establishing evidence-based recommendations regarding its use.
Regulatory agencies evaluate the safety and efficacy of N,N-Dimethyl-N-ethanolamine-containing products based on scientific evidence.
Compliance with regulatory requirements ensures that N,N-Dimethyl-N-ethanolamine meet quality standards and are safe for consumer use.

Consumers should be aware of the limitations of available evidence and exercise caution when using Deanol-containing products, particularly those marketed for cognitive enhancement.
Consulting healthcare professionals and reputable sources can help individuals make informed decisions about its use.
In cosmetics, N,N-Dimethyl-N-ethanolamine is often incorporated into formulations targeting skin care and hair care products.

N,N-Dimethyl-N-ethanolamine can act as a pH adjuster, emulsifier, or humectant, contributing to the stability, texture, and moisturizing properties of these products.
Some formulations may claim to have firming or toning effects on the skin due to N,N-Dimethyl-N-ethanolamine's potential to enhance skin elasticity.
While the exact mechanisms underlying N,N-Dimethyl-N-ethanolamine's purported cognitive-enhancing effects are not fully understood, some hypotheses suggest that it may influence cholinergic neurotransmission.

Cholinergic pathways play a crucial role in memory, attention, and learning processes.
N,N-Dimethyl-N-ethanolamine's interaction with these pathways may modulate neurotransmitter levels and neuronal activity, affecting cognitive function.
Ongoing research continues to explore N,N-Dimethyl-N-ethanolamine's potential therapeutic applications and mechanisms of action.

Studies may investigate its effects on neuroplasticity, neuroprotection, and neurotransmitter systems to elucidate its role in cognitive function and neurological disorders.
Additionally, clinical trials assessing N,N-Dimethyl-N-ethanolamine's efficacy and safety in specific populations, such as older adults or individuals with cognitive impairments, are warranted.
Amines are chemical bases.

They neutralize acids to form salts plus water.
These acid-base reactions are exothermic.
The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base.

Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.
Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
N,N-Dimethyl-N-ethanolamine may react vigorously with oxidizing materials.

N,N-Dimethyl-N-ethanolamine is used as a corrosion inhibitor; pharmaceutical intermediate; in making dyestuffs, textiles, pharmaceuticals; emulsifiers in paints and coatings.
Also, N,N-Dimethyl-N-ethanolamine has been used as a medication in the treatment ofbehavioral problems of children.
When administered orally, N,N-Dimethyl-N-ethanolamine acetamidobenzoate (the therapeutic salt formulation) has been shown to cross the blood-brain barrier (HSDB 1988).

Two other studies have examined the pharmacokinetics of dimethylaminoethanol in rats and healthy adults.
N,N-Dimethyl-N-ethanolamine is a chemical that can be converted into choline.
Choline is involved in a series of reactions that form acetylcholine, a chemical that is found in the brain and other areas of the body.

N,N-Dimethyl-N-ethanolamine is a "neurotransmitter" that helps nerve cells communicate.
N,N-Dimethyl-N-ethanolamine is used for attention deficit-hyperactivity disorder (ADHD), Alzheimer disease, autism, and other conditions, but there is no good scientific evidence to support these uses.

The exact mass of the compound N,N-Dimethyl-N-ethanolamine is 89.0841 and the complexity rating of the compound is unknown.
The solubility of this chemical has been described as greater than or equal to 100 mg/ml at 73° f (ntp, 1992)11.22 mmiscible with watermiscible with alcohol, ethermiscible with acetone, benzene1000 mg/mlsolubility in water: miscible.

Uses:
N,N-Dimethyl-N-ethanolamine is used as corrosion inhibitor, anti-scaling agent, paint additive, coating additive and solids separation agent.
N,N-Dimethyl-N-ethanolamine is used for the manufacture of: fabricated metal products, machinery and vehicles, mineral products (e.g. plasters, cement) and metals.
Other release to the environment of N,N-Dimethyl-N-ethanolamine 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.

N,N-Dimethyl-N-ethanolamine is used in the following products: polymers, coating products, fillers, putties, plasters, modelling clay and inks and toners.
Release to the environment of N,N-Dimethyl-N-ethanolamine can occur from industrial use: formulation of mixtures, manufacturing of the substance, formulation in materials, in the production of articles and as an intermediate step in further manufacturing of another substance (use of intermediates).
N,N-Dimethyl-N-ethanolamine is used in the following products: polymers, coating products and paper chemicals and dyes.

N,N-Dimethyl-N-ethanolamine has an industrial use resulting in manufacture of another substance (use of intermediates).
N,N-Dimethyl-N-ethanolamine is used in the following areas: formulation of mixtures and/or re-packaging and building & construction work.
N,N-Dimethyl-N-ethanolamine is used for the manufacture of: chemicals, pulp, paper and paper products, fabricated metal products, machinery and vehicles and plastic products.

Release to the environment of N,N-Dimethyl-N-ethanolamine can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates), in the production of articles, formulation in materials, for thermoplastic manufacture and as processing aid.
N,N-Dimethyl-N-ethanolamine is a precursor to other chemicals, such as the nitrogen mustard 2-dimethylaminoethyl chloride.
N,N-Dimethyl-N-ethanolamine is used in gas purification.

In certain chemical reactions, N,N-Dimethyl-N-ethanolamine can function as a catalyst, accelerating the rate of reaction without being consumed in the process.
N,N-Dimethyl-N-ethanolamine facilitates the conversion of reactants into desired products and may enhance reaction efficiency in various industrial processes.
N,N-Dimethyl-N-ethanolamine is incorporated into cosmetic formulations, including skin care products, hair care products, and toiletries.

N,N-Dimethyl-N-ethanolamine can serve multiple functions in these formulations, such as adjusting pH, emulsifying ingredients, and providing moisturizing or conditioning effects.
N,N-Dimethyl-N-ethanolamine is a common ingredient in some dietary supplements marketed for cognitive enhancement or brain health.
These supplements often claim to support memory, focus, and mental clarity, although scientific evidence supporting these claims is limited and controversial.

N,N-Dimethyl-N-ethanolamine is studied for its potential therapeutic effects in various health conditions, including neurodegenerative disorders and cognitive impairments.
Research explores its mechanisms of action, pharmacokinetics, and potential benefits as a treatment adjunct or therapeutic agent.
N,N-Dimethyl-N-ethanolamine can be used as an additive in polymer formulations to impart desired properties, such as enhanced flexibility, adhesion, or resistance to degradation.

N,N-Dimethyl-N-ethanolamine may improve the performance of polymeric materials in applications ranging from adhesives and coatings to plastics and composites.
N,N-Dimethyl-N-ethanolamine serves as a solvent or co-solvent, facilitating the dissolution of substances and aiding in the production of formulations or chemical mixtures.
N,N-Dimethyl-N-ethanolamine is solvent properties make it valuable in applications such as cleaning, degreasing, and extraction processes.

N,N-Dimethyl-N-ethanolamine can act as a surfactant, lowering the surface tension between two substances and promoting their mixing or dispersion.
N,N-Dimethyl-N-ethanolamine finds application in formulations such as detergents, emulsifiers, foaming agents, and dispersants in various industrial and household products.
N,N-Dimethyl-N-ethanolamine may be used as a dyeing assistant, leveling agent, or softening agent to improve the processing and quality of textile materials.

N,N-Dimethyl-N-ethanolamine can enhance dye uptake, uniformity of coloration, and fabric handle, contributing to the production of high-quality textiles.
N,N-Dimethyl-N-ethanolamine is utilized in gas treatment processes, particularly in the removal of acidic gases such as hydrogen sulfide (H2S) and carbon dioxide (CO2) from natural gas and biogas streams.
N,N-Dimethyl-N-ethanolamine can react with acidic components to form stable salts or complexes, thereby purifying the gas for various industrial applications.

In the printing industry, N,N-Dimethyl-N-ethanolamine may be incorporated into ink formulations as a solvent or additive to enhance print quality, adhesion, and drying characteristics.
N,N-Dimethyl-N-ethanolamine can help optimize ink performance and improve the printing process in applications such as offset printing, flexography, and gravure printing.
N,N-Dimethyl-N-ethanolamine is sometimes added to metalworking fluids, such as cutting oils and coolants, to improve lubricity, thermal stability, and corrosion protection during machining, grinding, and metal forming operations.

N,N-Dimethyl-N-ethanolamine enhances tool life, surface finish, and overall machining efficiency in metalworking processes.
In photographic applications, Deanol may be used in the formulation of developers, fixing agents, and other processing chemicals.
N,N-Dimethyl-N-ethanolamine plays a role in the development and stabilization of photographic images, contributing to the production of high-quality prints in traditional and digital photography.

N,N-Dimethyl-N-ethanolamine can serve as a catalyst or blowing agent in the production of polyurethane foams.
N,N-Dimethyl-N-ethanolamine promotes the polymerization reaction and facilitates the formation of cellular structures, leading to the production of flexible or rigid foams with desired properties such as density, resilience, and thermal insulation.
In water treatment and detergent formulations, N,N-Dimethyl-N-ethanolamine may act as a sequestering agent or chelating agent, binding to metal ions and preventing their precipitation or interference with chemical processes.

N,N-Dimethyl-N-ethanolamine helps improve water quality, prevent scale formation, and enhance the performance of cleaning products.
N,N-Dimethyl-N-ethanolamine is used in the synthesis of synthetic resins, including epoxy resins, polyurethane resins, and acrylic resins.
N,N-Dimethyl-N-ethanolamine contributes to the polymerization process, crosslinking reactions, or resin modification, leading to the production of resins with specific properties suitable for coatings, adhesives, and composite materials.

In coatings and paint formulations, N,N-Dimethyl-N-ethanolamine may be employed as a coalescing agent or viscosity modifier in waterborne systems.
N,N-Dimethyl-N-ethanolamine aids in film formation, film integrity, and flow properties, allowing for the production of environmentally friendly coatings with excellent performance and durability.
N,N-Dimethyl-N-ethanolamine can be utilized in wood preservation treatments to enhance the resistance of timber and wood products against decay, fungi, and insects.

N,N-Dimethyl-N-ethanolamine penetrates wood fibers, inhibits microbial growth, and prolongs the service life of wood structures in outdoor or humid environments.
N,N-Dimethyl-N-ethanolamine may have additional applications in diverse industries, including adhesives, sealants, lubricants, agricultural chemicals, and electronic materials.
N,N-Dimethyl-N-ethanolamine is multifunctional properties and compatibility with various substrates make it valuable in addressing specific performance requirements across different industrial sectors.

N,N-Dimethyl-N-ethanolamine is bitartrate salt is sold as a dietary supplement.
N,N-Dimethyl-N-ethanolamine has been also used as an ingredient in skin care.
N,N-Dimethyl-N-ethanolamine is used in Mood-enhancing products.

N,N-Dimethyl-N-ethanolamine serves as a precursor or intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and specialty chemicals.
N,N-Dimethyl-N-ethanolamine is utilized in organic synthesis reactions due to its amine functionality, contributing to the formation of complex molecules.
N,N-Dimethyl-N-ethanolamine is employed as a component in corrosion inhibitor formulations, particularly in industries where metal corrosion poses a significant challenge.

N,N-Dimethyl-N-ethanolamine helps mitigate corrosion by forming a protective layer on metal surfaces, thereby extending the lifespan of equipment and infrastructure.
N,N-Dimethyl-N-ethanolamine is also used as an intermediate for active pharmaceutical ingredients and dyes.
N,N-Dimethyl-N-ethanolamine serves as a curing agent for polyurethanes and epoxy resins.

Further, N,N-Dimethyl-N-ethanolamine is used as an additive to boiler water.
In addition to this, N,N-Dimethyl-N-ethanolamine is used therapeutically as a CNS stimulant.
MEA (DMAE) is also known as N,N-Dimethyl-N-ethanolamine.

Studies indicate skin-firming properties, and an ability to reduce the appearance of fine lines and wrinkles as well as dark circles under the eyes.
N,N-Dimethyl-N-ethanolamine is considered anti-aging, and antiinflammatory, and has exhibited free-radical scavenging activity.
N,N-Dimethyl-N-ethanolamine may be employed as a ligand in the copper-catalyzed amination of aryl bromides and iodides.

N,N-Dimethyl-N-ethanolamine is used as a chemical intermediate for antihistamines and local anesthetics; as a catalyst for curing epoxy resins and polyurethanes; and as a pH control agent for boiler water treatment.
However, N,N-Dimethyl-N-ethanolamine in the salt form, (i.e. dimethylaminoethanol acetamidobenzoate) is primarily utilized therapeutically as an antidepressant.
N,N-Dimethyl-N-ethanolamine is used as an aid for dispersing color pigments in water-based paints .

Furthermore, N,N-Dimethyl-N-ethanolamine is required as an intermediate product or starting material for the production of dyes , emulsifiers , corrosion inhibitors , textile auxiliaries, cosmetics and pharmaceuticals .
N,N-Dimethyl-N-ethanolamine is said to have a variety of positive effects, including nootropic effects , but there is a lack of clear evidence for this.
One author reports increased lucid dreams after using N,N-Dimethyl-N-ethanolamine.

N,N-Dimethyl-N-ethanolamine may be used as a ligand in the copper-catalyzed amination of aryl bromides and iodides.
N,N-Dimethyl-N-ethanolamine is used in the following products: laboratory chemicals, coating products, polymers, fillers, putties, plasters, modelling clay, lubricants and greases and adhesives and sealants.
N,N-Dimethyl-N-ethanolamine is used in the following areas: building & construction work, offshore mining and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.

Health Hazard:
N,N-Dimethyl-N-ethanolamine is classified as a mild skin irritant and a severe eye irritant.
Doses as high as 1200 mg daily produce no serious side effects and a single dose of 2500 mg taken in a suicide attempt had no adverse effects.
Inhalation of the vapor or mist can cause irritation to the upper respiratory tract.

Asthmatic symptoms have been reported.
Extremely irritating; may cause permanent eye injury. Corrosive; will cause severe skin damage with burns and blistering.
Ingestion may cause damage to the mucous membranes and gastrointestinal tract.

Safety Profile:
N,N-Dimethyl-N-ethanolamine causes increased blood pressure.
N,N-Dimethyl-N-ethanolamine can cause stomach upset, headaches & muscle tension.
Can lead to drowsiness, confusion and irritability.

Moderately toxic by ingestion, inhalation, skin contact, intraperitoneal, and subcutaneous routes.
A skin and severe eye irritant.
Used medically as a central nervous system stimulant.

Flammable liquid when exposed to heat or flame; can react vigorously with oxidzing materials.
Ignites spontaneously in contact with cellulose nitrate of high surface area.
To fight fire, use alcohol foam, foam, CO2, dry chemical.

N,N-Dimethyl-para-toluidine N,N-dimethyl-para-toluidine is used as a polymerization accelerator in the manufacture of bone cements and dental materials, in industrial glues, and as an intermediate in dye and pesticide synthesis. Thus, there is potential for human exposure to N,N-dimethyl-para-toluidine, an aromatic amine with a structural alert for potential DNA reactivity. The National Toxicology Program (NTP) is evaluating the toxicity and carcinogenicity of N,N-dimethyl-para-toluidine in male and female Fischer 344 rats and B6C3F1 mice. To aid in the design and interpretation of those studies, we have investigated the excretion and tissue distribution of oral and intravenous (IV) doses of radiolabeled N,N-dimethyl-para-toluidine in these strains of rodents. A single low (2.5 mg/kg), mid (25 mg/kg) or high (250 mg/kg) dose of carbon-14 labeled N,N-dimethyl-para-toluidine was administered. Excreta collected for up to 72 hr after dosing and tissues collected at sacrifice were analyzed for total radioactivity. Early studies were terminated at 72 hr. After a low IV dose to male rats ~100% of the dose was excreted and <2% was recovered in tissues at 72 hr. The high oral dose was acutely toxic to male mice. The same oral dose was not overtly toxic to male rats, and by 72 hr 86% of the dose was excreted and 2% remained in tissues. Subsequent studies were terminated at 24 hr to better understand the tissue distribution of radioactivity at earlier time points, which are more relevant to the interpretation of repeated dose toxicity studies. After the high oral dose to male rats ~18% of the dose was recovered in tissues and ~72% was excreted by 24 hr. In contrast, at the low and mid doses most of the radioactivity (~83-100%) was excreted by 24 hr and <5% remained in tissues. In summary, N,N-dimethyl-para-toluidine derived radioactivity was rapidly excreted by rats and mice after a single oral or IV dose and no striking sex differences in N,N-dimethyl-para-toluidine disposition were observed within a species. However, dose dependent differences in toxicity and disposition were observed. These data will be used to aid in the interpretation of safety/toxicity studies of N,N-dimethyl-para-toluidine conducted by the NTP. Product Information of N,N-Dimethyl-para-toluidine 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 The metabolism of orally administered N,N-dimethyl-p-toluidine (DMPT) in male F344 rats was investigated. The rat urinary metabolite profile was determined by analytical reverse-phase high performance liquid chromatography (HPLC). Four radiolabeled peaks were observed, isolated, and purified by solid-phase extraction (SPE) and preparative HPLC methods. The 4 peaks were identified as p-(N-acetylhydroxyamino)hippuric acid (M1), N,N-dimethyl-para-toluidine N-oxide (M2), N-methyl-p-toluidine (M3), and parent N,N-dimethyl-para-toluidine. Metabolites M1 and M2 were identified by spectrometric and spectroscopic methods, including mass fragmentation pattern identification from both liquid chromatography/mass spectrometry and gas chromatography/mass spectrometry, and from chemical analysis of nuclear magnetic resonance spectra. Structural confirmation of metabolite M2 was accomplished by comparison with a synthetic standard. Peaks M3 and the peak suspected to be N,N-dimethyl-para-toluidine were identified by comparison of their HPLC retention times and mass fragmentation patterns with authentic standards of N-methyl-p-toluidine and N,N-dimethyl-para-toluidine, respectively. N,N-dimethyl-para-toluidine metabolism is similar to that reported for N,N-dimethylaniline. IDENTIFICATION of N,N-Dimethyl-para-toluidine: N,N-dimethyl-para-toluidine is a colorless liquid to brown oil. It has an aromatic odor. It does not dissolve in water. USE of N,N-Dimethyl-para-toluidine: N,N-dimethyl-para-toluidine is used to make acrylic resins and denture materials. It is used in the cement in most hip and bone replacements. N,N-dimethyl-para-toluidine is also used to make dyes and pesticides, industrial glues, and artificial fingernail preparations. EXPOSURE of N,N-Dimethyl-para-toluidine: There is potential for widespread human exposure because of its use in dental materials and bone cements. If released to the environment, N,N-dimethyl-para-toluidine may be broken down rapidly in air. It travels through soil. It may volatilize from moist soil and water surfaces. However, it will exist partially as an ion. Ions do not volatilize. This type of ion is not likely to leach. It is not known if this chemical is biodegradable in soil or water. There is a potential for buildup in aquatic organisms. RISK: Some people with dental materials and bone cements containing N,N-dimethyl-para-toluidine have developed allergic reactions. In studies of rats and mice given N,N-dimethyl-para-toluidine by mouth 5 days per week for 3 months, early deaths occurred at doses equal to or greater than 125 mg/kg body weight. In surviving mice and rats, adverse effects were found in the blood, nose, lung and liver. Cancer was found in studies of rats and mice given N,N-dimethyl-para-toluidine by mouth 5 days per week for two years. In rats, liver and nose cancers were found. In mice, liver, lung and forestomach cancers were found. The California Environmental Protection Agency's Office of Environmental Health Hazard Assessment announced in April 2014 that it intends to list N,N-dimethyl-para-toluidine as known to the State to cause cancer. The U.S. EPA IRIS program, the International Agency for Research on Cancer, and the U.S. National Toxicology Program Twelfth Report on Carcinogens have not assessed the potential of N,N-dimethyl-para-toluidine to cause cancer in humans. N,N-dimethyl-para-toluidine is an accelerator in the redox initiator-accelerator system used commercially to cure methyl methacrylate monomers. Polymerization is rarely complete. N,N-dimethyl-para-toluidine is a high-production volume chemical with potential for widespread human exposure through its use in dental materials and bone cements. N,N-dimethyl-para-toluidine has been used in the preparation of acrylic denture materials for the past 50 years. It is used as the accelerator for the cement in most of the hip and bone replacements to activate the polymerization reaction at concentrations ranging from 0.7% to 2.6% . N,N-dimethyl-para-toluidine is found in industrial glues and artificial fingernail preparations and is used as an intermediate in dye and pesticide synthesis. It has a shorter setting time (11.5 minutes) than some alternative accelerators. Acryl resins used in dental practice are blends of poly(methyl methacrylated) particles and methyl methacrylate monomer, or copolymers of methyl methacrylate with styrene or other acrylic monomers. This blend is a slurry of high viscosity that is hardened by the free radical polymerization of the monomeric components. The hardening process is initiated by the decomposition of a small quantity of organic peroxides (1% to 3%; usually benzoyl peroxide) activated by the redox reaction with the tertiary amine. The tertiary amine, most often N,N-dimethyl-para-toluidine, is the ingredient that induces the reaction giving rise to free radicals capable of initiating polymerization of the acrylic monomers. Polymerization is rarely complete. Five commercially available bone cements were analysed by high-performance liquid chromatography for detecting the residual content of an accelerator, the amine N,N-dimethyl-p-toluidine (N,N-dimethyl-para-toluidine), after curing. It was found that the concentration of N,N-dimethyl-para-toluidine in aqueous extracts decreases with time, being almost absent 7 days after curing. Differences were noticed among the cements; residual N,N-dimethyl-para-toluidine is higher in cements prepared with higher content of the amine. It is verified that N,N-dimethyl-para-toluidine's toxic effect on cell cultures is dose-related; a delay in the cell replication cycle is induced in vitro. Damage is reversible, thus justifying the low bone cement toxicity that is clinically ascertained. The use of solid phase extraction (SPE) and high performance liquid chromatography (HPLC) for the analysis of toxic components eluted from methyl-methacrylate polymer (pMMA) dental materials was described. Two pMMA composite resins, Yunifast and Acron, were analyzed. Yunifast was polymerized at room temperature, and Acron at 100 degrees-C. Each sample was then placed in equine serum at room temperature, and serum was replaced daily. The serum extract was subjected to SPE and HPLC, for methyl-methacrylate, N,N-dimethyl-p-toluidine (N,N-dimethyl-para-toluidine), and benzoylperoxide (BPO) (initiator and stimulator for the polymerization) analysis. Results showed that the MMA and N,N-dimethyl-para-toluidine eluted was in the order of 10 to 100 parts per million. Almost negligible amounts of BPO and benzoic-acid were also eluted. A greater amount of these compounds was eluted from Yunifast, a more pliant material. N,N-dimethyl-para-toluidine showed greater elution than MMA. The hydrophilic portion of Yunifast was more cytotoxic than the hydrophobic portion, and contained BA and p-toluidine as major and minor components. The /study/ conclude that the rigidity of the material is critical to the extractable quantity, and recommend that both Yunifast and Acron be immersed in hot water before use in order to remove hydrophilic toxic compounds from these pMMA dental materials. The National Occupational Exposure Survey, which was conducted by the National Institute for Occupational Safety and Health (NIOSH) between 1981 and 1983, estimated that 62,720 workers were potentially exposed to N,N-dimethyl-para-toluidine in the workplace (NIOSH, 1990). There is potential for widespread human exposure to N,N-dimethyl-para-toluidine in occupational settings where bone cements, dental prostheses, industrial glues, and artificial fingernails are manufactured or used. Exposure to N,N-dimethyl-para-toluidine may be a concern because of the possible release of unreacted chemicals from polymeric composites. IDENTIFICATION AND USE of N,N-Dimethyl-para-toluidine: N,N-dimethyl-para-toluidine is a clear to yellow liquid with an aromatic odor; insoluble in water. N,N-dimethyl-para-toluidine is an accelerator in the redox initiator-accelerator system used commercially to cure methyl methacrylate monomers. It is a high-production volume chemical with potential for widespread human exposure through its use in dental materials and bone cements. N,N-dimethyl-para-toluidine has been used in the preparation of acrylic denture materials for the past 50 years. It is used as the accelerator for the cement in most of the hip and bone replacements to activate the polymerization reaction. N,N-dimethyl-para-toluidine is found in industrial glues and artificial fingernail preparations and is used as an intermediate in dye and pesticide synthesis. HUMAN EXPOSURE AND TOXICITY of N,N-Dimethyl-para-toluidine: Toxic by skin absorption and inhalation. Short-term exposure effects are mostly hematotoxic (methemoglobinemia causing cyanosis, brain damage and renal insufficiency) and may be delayed. Exposure to high concentrations may lead to death. An acute cyanotic episode due to methemoglobinemia occurred in a 16-month old girl following the ingestion of N,N-dimethyl-para-toluidine (6 mg/kg of body weight ) used in the production of artificial fingernails. Administration of methylene blue was effective in the reversal of the methemoglobinemia. In vitro studies suggest that the activity of the compound was probably due to its biochemical transformation to the toxic metabolite p-methylphenylhydroxylamine. There is potential for widespread human exposure to N,N-dimethyl-para-toluidine in occupational settings where bone cements, dental prostheses, industrial glues, and artificial fingernails are manufactured or used. Exposure to N,N-dimethyl-para-toluidine may be a concern because of the possible release of unreacted chemicals from polymeric composites. "Sniffing" glue is one possible means of exposure to N,N-dimethyl-para-toluidine. Contact allergy to N,N-dimethyl-para-toluidine was reported in 3 cases among 22 patients with the burning mouth syndrome who wore complete or partial dentures. ANIMAL STUDIES of N,N-Dimethyl-para-toluidine: Under the conditions of the NTP 2-year oral gavage studies, there was clear evidence of carcinogenic activity of N,N-dimethyl-para-toluidine in rats based on increased incidences of hepatocellular carcinoma, and hepatocellular adenoma or carcinoma (combined) in male and female rats, and increased incidences of nasal cavity neoplasms (primarily nasal cavity transitional epithelium adenoma) in male rats. There was clear evidence of carcinogenic activity of N,N-dimethyl-para-toluidine in mice based on increased incidences of hepatocellular adenoma (multiple), hepatocellular carcinoma, and hepatoblastoma in male and female mice, and increased incidences of alveolar/ bronchiolar neoplasms (primarily adenoma)in female mice. Administration of N,N-dimethyl-para-toluidine resulted in increased incidences of nonneoplastic lesions of the liver and nasal cavity in male and female rats and mice; the kidney in male and female rats; the spleen and bone marrow in male and female rats and female mice; the lung in male and female mice; the forestomach in male rats and female mice; the mesenteric lymph node in male rats and female mice; and the olfactory lobe in male and female mice. N,N-dimethyl-para-toluidine also caused hematologic toxicity and increases in methemoglobin levels in male and female rats and mice (as measured at 3 months). N,N-dimethyl-para-toluidine was tested in two independent bacterial gene mutation studies; both studies gave negative results in S. typhimurium or E. coli tester strains, with and without exogenous metabolic activation. No significant increases in the frequencies of micronucleated erythrocytes were observed in peripheral blood of male or female mice treated with N,N-dimethyl-para-toluidine by gavage for 3 months. Furthermore, no increases in micronucleated reticulocytes were observed in male mice treated with N,N-dimethyl-para-toluidine for 4 days. Results of DNA damage (comet) studies yielded mixed results. No increases in DNA damage (measured as percent tail DNA) were seen in liver cells or blood leukocytes of male mice administered N,N-dimethyl-para-toluidine by gavage once daily for 4 days. However, a small but significant increase in DNA damage was seen in liver cells of male rats administered 60 mg/kg N,N-dimethyl-para-toluidine once daily for 4 days. It was also tested for structural and numerical chromosome aberrations in hamster V79 cells (micronucleus test, matched with an immunofluorescent staining for kinetochore proteins), and in vivo DNA damage in mouse and rat liver (alkaline DNA elution test). The results essentially indicate that the chemical is a chromosome damaging agent. In two in vivo alkaline elution assays, Sprague-dawley rats were administered N,N-dimethyl-para-toluidine via oral or intraperitoneal injection at up to 1080 mg/kg-bw for up to 24 hours. DNA fragmentation increased in liver cells to about 2.4 times the control at the highest dose only and suggested that N,N-dimethyl-para-toluidine was weakly positive in this assay. Negative results were obtained when N,N-dimethyl-para-toluidine was tested in Balb/c mice. N,N-dimethyl-para-toluidine induced chromosomal effects in these assay. In a cytogenetic assay, Chinese Hamster V79 cells were exposed to N,N-dimethyl-para-toluidine up to 1.2mM without metabolic activation. Cytotoxicity was observed at 1.2 mM, where > 10% survival was estimated by colony formation. It is not clear if positive controls were used. N,N-dimethyl-para-toluidine induced chromosomal aberrations in this assay. CONCLUSIONS Under the conditions of these 2-year oral gavage studies, there was clear evidence of carcinogenic activity* of N,N-dimethyl-para-toluidine in male F344/N rats based on increased incidences of hepatocellular carcinoma, and hepatocellular adenoma or carcinoma (combined), and increased incidences of nasal cavity neoplasms (primarily nasal cavity transitional epithelium adenoma). The increased incidences of thyroid gland follicular cell neoplasms may have been related to treatment. There was clear evidence of carcinogenic activity of N,N-dimethyl-para-toluidine in female F344/N rats based on increased incidences of hepatocellular carcinoma and hepatocellular adenoma or carcinoma (combined). The occurrence of nasal cavity transitional epithelium adenoma was considered to be related to treatment. There was clear evidence of carcinogenic activity of N,N-dimethyl-para-toluidine in male B6C3F1/N mice based on increased incidences of hepatocellular adenoma (multiple), hepatocellular carcinoma, and hepatoblastoma. There was clear evidence of carcinogenic activity of N,N-dimethyl-para-toluidine in female B6C3F1/N mice based on increased incidences of hepatocellular adenoma, hepatocellular carcinoma, and hepatoblastoma and increased incidences of alveolar/ bronchiolar neoplasms (primarily adenoma). The increased incidences of forestomach squamous cell papilloma in female mice were considered to be related to treatment. Administration of N,N-dimethyl-para-toluidine resulted in increased incidences of nonneoplastic lesions of the liver and nasal cavity in male and female rats and mice; the kidney in male and female rats; the spleen and bone marrow in male and female rats and female mice; the lung in male and female mice; the forestomach in male rats and female mice; the mesenteric lymph node in male rats and female mice; and the olfactory lobe in male and female mice. N,N-dimethyl-para-toluidine also caused hematologic toxicity and increases in methemoglobin levels in male and female rats and mice (as measured at 3 months). N,N-dimethyl-para-toluidine's production and use as a polymerization accelerator in the manufacture of bone cements and dental materials, in industrial glues, and as an intermediate in dye and pesticide synthesis may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 0.178 mm Hg at 25 °C indicates N,N-dimethyl-para-toluidine will exist solely as a vapor in the atmosphere. Vapor-phase N,N-dimethyl-para-toluidine 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 2 hrs. N,N-dimethyl-para-toluidine does not contains chromophores that absorb at wavelengths >290 nm and, therefore, is not expected to be susceptible to direct photolysis by sunlight. If released to soil, N,N-dimethyl-para-toluidine is expected to have moderate mobility based upon an estimated Koc of 260. The pKa of N,N-dimethyl-para-toluidine is 5.63, indicating that this compound will exist partially in the cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts. Volatilization of the neutral species from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 7.0X10-5 atm-cu m/mole. N,N-dimethyl-para-toluidine is not expected to volatilize from dry soil surfaces based upon its vapor pressure. Biodegradation data in soil or water were not available. If released into water, N,N-dimethyl-para-toluidine is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. 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 1 and 10 days, respectively. An estimated BCF of 33 suggests the potential for bioconcentration in aquatic organisms is moderate. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions (pH 5 to 9). Occupational exposure to N,N-dimethyl-para-toluidine may occur through inhalation and dermal contact with this compound at workplaces where N,N-dimethyl-para-toluidine is produced or used. N,N-dimethyl-para-toluidine's production and use as a polymerization accelerator in the manufacture of bone cements and dental materials, in industrial glues, and as an intermediate in dye and pesticide synthesis may result in its release to the environment through various waste streams. Based on a classification scheme, an estimated Koc value of 260, determined from a log Kow of 2.81 and a regression-derived equation, indicates that N,N-dimethyl-para-toluidine is expected to have moderate mobility in soil. The pKa of N,N-dimethyl-para-toluidine is 5.63, indicating that this compound will exist partially in the cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts. Volatilization of the neutral species of N,N-dimethyl-para-toluidine from moist soil surfaces is expected to be an important fate process given an estimated Henry's Law constant of 7.0X10-5 atm-cu m/mole, derived from its vapor pressure, 0.178 mm Hg, and water solubility, 455 mg/L. N,N-dimethyl-para-toluidine is not expected to volatilize from dry soil surfaces based upon its vapor pressure. Biodegradation data in soil were not available. According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere, N,N-dimethyl-para-toluidine, which has a vapor pressure of 0.178 mm Hg at 25 °C, is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase N,N-dimethyl-para-toluidine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 2 hrs, calculated from its rate constant of 2.0X10-10 cu cm/molecule-sec at 25 °C that was derived using a structure estimation method. N,N-dimethyl-para-toluidine does not contain chromophores that absorb at wavelengths >290 nm and, therefore, is not expected to be susceptible to direct photolysis by sunlight. The rate constant for the vapor-phase reaction of N,N-dimethyl-para-toluidine with photochemically-produced hydroxyl radicals has been estimated as 2.0X10-10 cu cm/molecule-sec at 25 °C using a structure estimation method. This corresponds to an atmospheric half-life of about 2 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm. N,N-dimethyl-para-toluidine is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions. N,N-dimethyl-para-toluidine does not contain chromophores that absorb at wavelengths >290 nm and, therefore, is not expected to be susceptible to direct photolysis by sunlight. The Koc of N,N-dimethyl-para-toluidine is estimated as 260, using a log Kow of 2.81 and a regression-derived equation. According to a classification scheme, this estimated Koc value suggests that N,N-dimethyl-para-toluidine is expected to have moderate mobility in soil. The pKa of N,N-dimethyl-para-toluidine is 5.63, indicating that this compound will exist partially in the cation form and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts. A Kd value of 380 for sorption to monmorillonite has been reported. The Henry's Law constant for N,N-dimethyl-para-toluidine is estimated as 7.0X10-5 atm-cu m/mole derived from its vapor pressure, 0.178 mm Hg, and water solubility, 455 mg/L. This Henry's Law constant indicates that N,N-dimethyl-para-toluidine is expected to volatilize from water surfaces. 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) is estimated as 1 day. The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as 10 days. N,N-dimethyl-para-toluidine's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur. N,N-dimethyl-para-toluidine is not expected to volatilize from dry soil surfaces based upon its vapor pressure. About N,N-dimethyl-para-toluidine N,N-dimethyl-para-toluidine 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. N,N-dimethyl-para-toluidine is used by professional workers (widespread uses), in formulation or re-packing and at industrial sites. Consumer Uses of N,N-dimethyl-para-toluidine ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which N,N-dimethyl-para-toluidine is most likely to be released to the environment. Article service life of N,N-dimethyl-para-toluidine ECHA has no public registered data on the routes by which N,N-dimethyl-para-toluidine is most likely to be released to the environment. ECHA has no public registered data indicating whether or into which articles the substance might have been processed. Widespread uses by professional workers of N,N-dimethyl-para-toluidine N,N-dimethyl-para-toluidine is used in the following products: pH regulators and water treatment products, adhesives and sealants, leather treatment products and laboratory chemicals. N,N-dimethyl-para-toluidine is used in the following areas: health services and scientific research and development. N,N-dimethyl-para-toluidine is used for the manufacture of: textile, leather or fur. Other release to the environment of N,N-dimethyl-para-toluidine 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). Formulation or re-packing of N,N-dimethyl-para-toluidine N,N-dimethyl-para-toluidine is used in the following products: adhesives and sealants. Release to the environment of N,N-dimethyl-para-toluidine can occur from industrial use: formulation of mixtures. Uses at industrial sites of N,N-dimethyl-para-toluidine N,N-dimethyl-para-toluidine is used in the following products: adhesives and sealants, textile treatment products and dyes, pH regulators and water treatment products and laboratory chemicals. N,N-dimethyl-para-toluidine has an industrial use resulting in manufacture of another substance (use of intermediates). N,N-dimethyl-para-toluidine is used in the following areas: formulation of mixtures and/or re-packaging, health services and scientific research and development. N,N-dimethyl-para-toluidine is used for the manufacture of: chemicals. Release to the environment of N,N-dimethyl-para-toluidine can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), in processing aids at industrial sites and as processing aid. Manufacture of N,N-dimethyl-para-toluidine ECHA has no public registered data on the routes by which N,N-dimethyl-para-toluidine is most likely to be released to the environment.

N,N-Dimethyl-p-toluidine (DMPT) is a versatile organic compound extensively utilized in scientific research.
As a colorless, crystalline solid, N,N-Dimethyl-p-toluidine (DMPT) easily dissolves in most organic solvents.
N,N-Dimethyl-p-toluidine (DMPT) is an organic compound with formula (CH3)3C6H2NH2.

CAS Number: 99-97-8
Molecular Formula: C9H13N
Molecular Weight: 135.21
EINECS Number: 202-805-4

N,N-Dimethyl-p-toluidine, 99-97-8, N,N,4-TRIMETHYLANILINE, 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, 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-, 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-DIMETHYL-P-TOLUIDINE [IARC], NCGC00091397-01, NCGC00091397-02, NCGC00091397-03, NCGC00254201-01, NCGC00258922-01, SMR001216586, D0807, FT-0629511, FT-0636092, FT-0656134, NS00002247, 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-Dimethyl-p-toluidine (DMPT) is an aromatic amine that is of commercial interest as a precursor to dyes.
N,N-Dimethyl-p-toluidine (DMPT) is prepared by selective nitration of mesitylene, avoiding oxidation of the methyl groups, followed by reduction of the resulting nitro group to the aniline.
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 N,N-Dimethyl-p-toluidine (DMPT) is wide range of applications, N,N-Dimethyl-p-toluidine serves as a crucial reagent for the synthesis of various compounds in laboratory settings.
N,N-Dimethyl-p-toluidine (DMPT) is applications span across the synthesis of numerous compounds, including,agrochemicals, pesticides, amino acids, peptides, and nucleotides.
N,N-Dimethyl-p-toluidine (DMPT) is a tertiary amine that can undergo iron-catalyzed oxidative C-C coupling with phenylacetylene and benzamide in the presence of tert-butylperoxide to form N,4-dimethyl-N-(3-phenylprop-2-ynyl)benzenamine and N-((methyl(p-tolyl)amino)methyl)benzamide, respectively.

N,N-Dimethyl-p-toluidine (DMPT) 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.
N,N-Dimethyl-p-toluidine (DMPT) is presented to the CSWG for review because it is a highproduction-volume chemical that has the potential for widespread human exposure from its use in dental materials and bone cements.
N,N-Dimethyl-p-toluidine (DMPT) is used in the following products: pH regulators and water treatment products, adhesives and sealants, leather treatment products and laboratory chemicals.

N,N-Dimethyl-p-toluidine (DMPT) is used in the following areas: health services and scientific research and development. N,N-dimethyl-para-toluidine is used for the manufacture of: textile, leather or fur.
N,N-Dimethyl-p-toluidine (DMPT) is used in the following products: adhesives and sealants.
Release to the environment of N,N-Dimethyl-p-toluidine (DMPT) can occur from industrial use: formulation of mixtures.

N,N-Dimethyl-p-toluidine (DMPT) is used in the following products: adhesives and sealants, textile treatment products and dyes, pH regulators and water treatment products and laboratory chemicals.
N,N-Dimethyl-p-toluidine (DMPT) has an industrial use resulting in manufacture of another substance (use of intermediates).
N,N-Dimethyl-p-toluidine (DMPT) is the accelerator in the redox initiator-accelerator system used commercially to cure methyl methacrylate monomers.

Polymerization is rarely complete; N,N-Dimethyl-p-toluidine (DMPT) retained in bone cements and dental materials is sufficient to cause exposure to surgical staff, dental prosthetic device manufacturers, and denture wearers, among others.
Other release to the environment of N,N-Dimethyl-p-toluidine (DMPT) 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).
N,N-Dimethyl-p-toluidine (DMPT) finds utility in the creation of polymers, dyes, and catalysts.

N,N,4-trimethylaniline is a chemical compound with the molecular formula C9H13N.
N,N-Dimethyl-p-toluidine (DMPT) is thought to be the causative agent in “burning mouth” observed in denture wearers and it may be responsible for aseptic loosening of hip replacements
N,N-Dimethyl-p-toluidine (DMPT) is used in the following areas: formulation of mixtures and/or re-packaging, health services and scientific research and development.

N,N-Dimethyl-p-toluidine (DMPT) is used for the manufacture of: chemicals
N,N-Dimethyl-p-toluidine (DMPT) is a building block to a variety of bulky ligands.
Condensation with glyoxal gives the 1,2-diimine ligands.

An example is glyoxal-bis(mesitylimine), a yellow solid that is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal.
The diimine is a useful precursor to popular NHC ligands including IMes.
N,N-Dimethyl-p-toluidine (DMPT), as found in 2nd generation Grubbs' catalyst, are also prepared from this compound.

The metabolism of orally administered N,N-Dimethyl-p-toluidine (DMPT) in male F344 rats was investigated.
The rat urinary metabolite profile was determined by analytical reverse-phase high performance liquid chromatography (HPLC).
Four radiolabeled peaks were observed, isolated, and purified by solid-phase extraction (SPE) and preparative HPLC methods.

The 4 peaks were identified as p-(Nacetylhydroxyamino)hippuric acid (M1), N,N-dimethyl-para-toluidine N-oxide (M2), N-methyl-p-toluidine (M3), and parent N,Ndimethyl-para-toluidine.
Metabolites M1 and M2 were identified by spectrometric and spectroscopic methods, including mass fragmentation pattern identification from both liquid chromatography/mass spectrometry and gas chromatography/mass spectrometry, and from chemical analysis of nuclear magnetic resonance spectra.
Structural confirmation of metabolite M2 was accomplished by comparison with a synthetic standard.

Peaks M3 and the peak suspected to be N,N-Dimethyl-p-toluidine (DMPT) were identified by comparison of their HPLC retention times and mass fragmentation patterns with authentic standards of N-methyl-ptoluidine and N,N-dimethyl-para-toluidine, respectively.
N,N-Dimethyl-p-toluidine (DMPT) is an aromatic amine, specifically a derivative of aniline where three methyl groups (-CH3) are substituted onto the nitrogen atom of the amine group.

N,N-Dimethyl-p-toluidine (DMPT) is a N-methyl-N-alkylaniline.
N,N-Dimethyl-p-toluidine (DMPT) is reaction with vinyl ether catalyzed by CuCl2 has been reported to afford tetrahydroquinolines.
N,N-Dimethyl-p-toluidine (DMPT) metabolism is similar to that reported for N,Ndimethylaniline.

N,N-Dimethyl-p-toluidine (DMPT) has a triarylamine structure with one 2,4,6-methylated phenyl and two 4-brominated phenyl rings.
The two bromo functional groups at the end of each benzene rings enable it to extend its conjugation via Suzuki, Yamamoto or Stille coupling reactions.
N,N-Dimethyl-p-toluidine (DMPT) is a convenient intermediate for the synthesis of polytriarylamines (PTAAs) via Yamamoto polycondensation.

PTAAs are electron rich thus commonly used as electron transport layer for perovskite solar cells and OLED devices.
PTAAs can normally be deposited by solution processing at lower temperature, significantly reducing possible thermal damage to the active layer.
N,N-Dimethyl-p-toluidine (DMPT) is prepared from the reaction of 2,4,6-trimethylaniline with 1-bromo-4-iodobenzene (Buchwald-Hartwig amination) in the presence of 1,1′-ferrocenediyl-bis(diphenylphosphine) (dppf) and sodium tert-butoxide in toluene.

N,N-Dimethyl-p-toluidine (DMPT) showed greater elution than MMA.
The hydrophilic portion of Yunifast was more cytotoxic than the hydrophobic portion, and contained BA and p-toluidine as major and minor components.
The /study/ conclude that the rigidity of the material is critical to the extractable quantity, and recommend that both Yunifast and Acron be immersed in hot water before use in order to remove hydrophilic toxic compounds from these pMMA dental materials.

The National Occupational Exposure Survey, which was conducted by the National Institute for Occupational Safety and Health (NIOSH) between 1981 and 1983, estimated that 62,720 workers were potentially exposed to N,N-Dimethyl-p-toluidine (DMPT) in the workplace (NIOSH, 1990).
There is potential for widespread human exposure to N,N-dimethyl-para-toluidine in occupational settings where bone cements, dental prostheses, industrial glues, and artificial fingernails are manufactured or used.
Exposure to N,N-Dimethyl-p-toluidine (DMPT) may be a concern because of the possible release of unreacted chemicals from polymeric composites.

The rate constant for the vapor-phase reaction of N,N-Dimethyl-p-toluidine (DMPT) with photochemically-produced hydroxyl radicals has been estimated as 2.0X10-10 cu cm/molecule-sec at 25 °C using a structure estimation method.
This corresponds to an atmospheric half-life of about 2 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm.
N,N-Dimethyl-p-toluidine (DMPT) is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions.

N,N-Dimethyl-p-toluidine (DMPT) does not contain chromophores that absorb at wavelengths >290 nm and, therefore, is not expected to be susceptible to direct photolysis by sunlight.
Being a tertiary amine, N,N-Dimethyl-p-toluidine (DMPT) is less basic than primary or secondary amines.
However, N,N-Dimethyl-p-toluidine (DMPT) can still act as a weak base in chemical reactions.

N,N-Dimethyl-p-toluidine (DMPT) can be synthesized through various methods, including the alkylation of aniline using methylating agents.
The specific synthetic route may depend on the intended application.
N,N-Dimethyl-p-toluidine (DMPT) and related aromatic amines can find applications in various industrial processes.

They may be used in the synthesis of dyes, pigments, pharmaceuticals, and other specialty chemicals.
Aromatic amines, including N,N-Dimethyl-p-toluidine (DMPT), are important intermediates in the synthesis of azo dyes.
Azo dyes are a significant class of synthetic dyes widely used in the textile and other industries.

N,N-Dimethyl-p-toluidine (DMPT) can serve as a chemical intermediate in the synthesis of various compounds.
N,N-Dimethyl-p-toluidine (DMPT) is reactivity allows for the creation of diverse chemical structures.
Like many aromatic amines, N,N-Dimethyl-p-toluidine (DMPT) may pose health and safety risks, and precautions should be taken when handling this compound.

N,N-Dimethyl-p-toluidine (DMPT) is a clear to yellow liquid with an aromatic odor; insoluble in water.
N,N-Dimethyl-p-toluidine (DMPT) is an accelerator in the redox initiator-accelerator system used commercially to cure methyl methacrylate monomers.
N,N-Dimethyl-p-toluidine (DMPT) is a high-production volume chemical with potential for widespread human exposure through its use in dental materials and bone cements.

N,N-Dimethyl-p-toluidine (DMPT) has been used in the preparation of acrylic denture materials for the past 50 years.
N,N-Dimethyl-p-toluidine (DMPT) belongs to the class of substituted anilines, which are organic compounds containing an amino group attached to a benzene ring.
The presence of the three methyl groups makes N,N-Dimethyl-p-toluidine (DMPT) a tertiary amine.

N,N-Dimethyl-p-toluidine (DMPT), is the ingredient that induces the reaction giving rise to free radicals capable of initiating polymerization of the acrylic monomers. Polymerization is rarely complete.
Five commercially available bone cements were analysed by high-performance liquid chromatography for detecting the residual content of an accelerator, the amine N,N-Dimethyl-p-toluidine (DMPT), after curing.
It was found that the concentration of N,N-Dimethyl-p-toluidine (DMPT) in aqueous extracts decreases with time, being almost
absent 7 days after curing.

Differences were noticed among the cements; residual N,N-Dimethyl-p-toluidine (DMPT) is higher in cements prepared with higher content of the amine.
N,N-Dimethyl-p-toluidine (DMPT) is verified that N,N-dimethyl-para-toluidine's toxic effect on cell cultures is dose-related; a delay in the cell replication cycle is induced in vitro.
Damage is reversible, thus justifying the low bone cement toxicity that is clinically ascertained.

The use of solid phase extraction (SPE) and high performance liquid chromatography (HPLC) for the analysis of toxic components eluted from methyl-methacrylate polymer (pMMA) dental materials was described.
N,N-Dimethyl-p-toluidine (DMPT) is used as the accelerator for the cement in most of the hip and bone replacements to activate the polymerization reaction.
N,N-Dimethyl-p-toluidine (DMPT) is found in industrial glues and artificial fingernail preparations and is used as an intermediate in dye and pesticide synthesis.

N,N-Dimethyl-p-toluidine (DMPT) is a fine chemical that belongs to the family of aminomethyl compounds.
N,N-Dimethyl-p-toluidine (DMPT)'s estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur.
N,N-Dimethyl-p-toluidine (DMPT) is not expected to volatilize from dry soil surfaces based upon its vapor pressure.

N,N-Dimethyl-p-toluidine (DMPT) is a versatile building block that can be used in the synthesis of complex compounds and as a reagent or speciality chemical in research.
N,N-Dimethyl-p-toluidine (DMPT) is also a useful intermediate for reactions and scaffolds in organic syntheses.
N,N-Dimethyl-p-toluidine (DMPT) can be used as an alternative to the more commonly used 4-aminophenol.

This compound has been observed to have high purity and quality with no detectable impurities.
N,N-Dimethyl-p-toluidine (DMPT) is used as a polymerization accelerator in the manufacture of bone cements and dental materials, in industrial glues, and as an intermediate in dye and pesticide synthesis.
Thus, there is potential for human exposure to N,N-Dimethyl-p-toluidine (DMPT), an aromatic amine with a structural alert for potential DNA reactivity.

The National Toxicology Program (NTP) is evaluating the toxicity and carcinogenicity of
N,N-Dimethyl-p-toluidine (DMPT) in male and female Fischer 344 rats and B6C3F1 mice.
N,N-Dimethyl-p-toluidine (DMPT) is radical cation undergoes reaction with the anthracene radical anion and generation of electrogenerated chemiluminescence (ECL) has been observed.

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. Combustible. Incompatible with strong oxidizing agents.
InChIKey: GYVGXEWAOAAJEU-UHFFFAOYSA-N
LogP: 1.729-2.81 at 35℃

N,N-Dimethyl-p-toluidine (DMPT) has been used in the preparation of acrylic denture materials for the past 50 years.
N,N-Dimethyl-p-toluidine (DMPT) is reactivity allows it to participate in a variety of chemical reactions.
Some aromatic amines, including certain derivatives, are known to exhibit catalytic activity in specific reactions.

Researchers may explore their catalytic potential in various transformations.
The use of the term N,N-Dimethyl-p-toluidine (DMPT) suggests the presence of three methyl groups on the nitrogen atom.
The specific isomerism, stereochemistry, and substitution pattern on the aromatic ring can affect the compound's properties.

Aromatic amines, including N,N-Dimethyl-p-toluidine (DMPT), can be analyzed using various analytical techniques, such as chromatography and spectroscopy.
These methods are employed for identification and quantification in research and industrial settings.
Like many chemical compounds, N,N-Dimethyl-p-toluidine (DMPT) requires careful handling due to potential health hazards.

This includes the use of appropriate personal protective equipment, adherence to safety protocols, and awareness of its potential toxicity.
Aromatic amines are commonly employed in research laboratories for their versatility in organic synthesis.
Researchers may study their properties and reactivity to develop new methodologies or create novel compounds.

Some aromatic amines serve as building blocks in the synthesis of pharmaceuticals and bioactive compounds.
N,N-Dimethyl-p-toluidine (DMPT) is used as the accelerator for the cement in most of the hip and bone replacements to activate the polymerization reaction at concentrations ranging from 0.7% to 2.6%.
N,N-Dimethyl-p-toluidine (DMPT) is found in industrial glues and artificial fingernail preparations and is used as an intermediate in dye and pesticide synthesis.

N,N-Dimethyl-p-toluidine (DMPT) has a shorter setting time (11.5 minutes) than some alternative accelerators.
As an aromatic amine, N,N-Dimethyl-p-toluidine (DMPT) exhibits reactivity typical of such compounds.
N,N-Dimethyl-p-toluidine (DMPT) can undergo reactions like aromatic substitution, where the hydrogen atoms on the aromatic ring can be replaced by other functional groups.

Some aromatic amines, depending on their structures, have been studied for their potential impact on biological systems and the environment.
Aromatic amines may find applications in biocatalysis and enzymatic reactions, where certain enzymes can catalyze specific transformations involving these compounds.
Acryl resins used in dental practice are blends of poly(methyl methacrylated) particles and methyl methacrylate monomer, or copolymers of methyl methacrylate with styrene or other acrylic monomers.

This blend is a slurry of high viscosity that is hardened by the free radical polymerization of the monomeric components.
N,N-Dimethyl-p-toluidine (DMPT)'s production and use as a polymerization accelerator in the manufacture of bone cements and dental materials, in industrial glues, and as an intermediate in dye and pesticide synthesis may result in its release to the environment through various waste streams.
If released to air, a vapor pressure of 0.178 mm Hg at 25 °C indicates N,N-Dimethyl-p-toluidine (DMPT) will exist solely as a vapor in the atmosphere.

Vapor-phase N,N-dimethyl-para-toluidine 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 2 hrs.
N,N-Dimethyl-p-toluidine (DMPT) does not contains chromophores that absorb at wavelengths >290 nm and, therefore, is not expected to be susceptible to direct photolysis by sunlight.
If released to soil, N,N-Dimethyl-p-toluidine (DMPT) is expected to have moderate mobility based upon an estimated Koc of 260.

The pKa of N,N-Dimethyl-p-toluidine (DMPT) is 5.63, indicating that this compound will exist partially in the cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts.
Volatilization of the neutral species from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 7.0X10-5 atm-cu m/mole.
N,N-Dimethyl-p-toluidine (DMPT) is not expected to volatilize from dry soil surfaces based upon its vapor pressure.

Biodegradation data in soil or water were not available.
If released into water, N,N-Dimethyl-p-toluidine (DMPT) is not expected to adsorb to suspended solids and sediment based upon the estimated Koc.
Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant.

Estimated volatilization halflives for a model river and model lake are 1 and 10 days, respectively.
An estimated BCF of 33 suggests the potential for bioconcentration in aquatic organisms is moderate.
Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions (pH 5 to 9).

Occupational exposure to N,N-Dimethyl-p-toluidine (DMPT) may occur through inhalation and dermal contact with this compound at workplaces where N,N-dimethyl-para-toluidine is produced or used.
These compounds may be subject to regulations to minimize their release and exposure.
N,N-Dimethyl-p-toluidine (DMPT), like other aromatic amines, can be utilized in organic synthesis for the preparation of various organic compounds.

N,N-Dimethyl-p-toluidine (DMPT) 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.

N,N-Dimethyl-p-toluidine (DMPT) is an accelerator in the redox initiator-accelerator system used commercially to cure methyl methacrylate monomers.
Polymerization is rarely complete.
N,N-Dimethyl-p-toluidine (DMPT) is a high-production volume chemical with potential for widespread human exposure through its
use in dental materials and bone cements.

Uses:
N,N-Dimethyl-p-toluidine (DMPT) is likely used in research laboratories for organic synthesis and chemical studies.
N,N-Dimethyl-p-toluidine (DMPT) is reactivity and properties may be explored in the development of new methodologies or understanding structure-activity relationships.
In research and educational settings, N,N-Dimethyl-p-toluidine (DMPT) may be used as a reagent in various laboratory experiments and demonstrations.

Some aromatic amines may have the ability to form complexes with metal ions, which can have applications in areas such as metal extraction and separation.
In metal surface treatment processes, aromatic amines might be employed as additives or components in formulations to enhance surface properties.
Certain aromatic amines are investigated for their electrochemical properties, making them potential candidates for use in batteries, sensors, or other electrochemical devices.

Some aromatic amines have been studied in the context of cancer research due to their potential mutagenic and carcinogenic properties.
Understanding their effects can contribute to cancer prevention strategies.
Aromatic amines may be involved in supramolecular chemistry studies, exploring the assembly of molecules into larger, organized
structures through non-covalent interactions.

In the field of tissue engineering, certain aromatic amines may be explored for their potential role in the development of biomaterials and scaffolds.
Some aromatic amines with specific optical properties are investigated for their potential use in photothermal therapy, a medical treatment that utilizes light-absorbing substances to generate heat and selectively destroy targeted cells.
Certain aromatic amines are studied for their potential as hydrogen storage materials in the context of alternative energy research.

Aromatic amines, due to their chemical properties, may be involved in certain wastewater treatment processes for the removal of pollutants and contaminants.
In the plastics and textile industries, certain aromatic amines are utilized as antistatic agents to reduce static electricity buildup.
Aromatic amines, particularly those with specific electronic properties, are investigated for their potential use in gas sensing devices for the detection of gases and vapors.

Some aromatic amines play a role in the development of materials used in photovoltaic devices and solar cells.
Aromatic amines may be included in formulations for surface coatings to enhance adhesion, flexibility, and resistance to environmental factors.
In the field of agrochemicals, certain aromatic amines may be components of formulations for pesticides or plant growth regulators.

Aromatic amines are subjects of study in material science, where their properties and reactivity are explored for the design and development of new materials with specific functionalities.
Aromatic amines can be involved as catalysts in certain hydrogenation reactions, facilitating the addition of hydrogen to unsaturated compounds.
In certain metal extraction processes, aromatic amines may be used as extractants for the separation of metals from ores or solutions.

Aromatic amines, including N,N,4-trimethylaniline, may find applications in the polymer industry.
They can be used as monomers or additives in the synthesis of certain polymers.
Some aromatic amines are utilized in the formulation of adhesives, where they can contribute to the chemical and physical properties of the adhesive.

Certain aromatic amines may have antioxidant properties.
While the specific antioxidant properties of N,N,4-trimethylaniline need to be assessed, some aromatic amines are known for their ability to inhibit oxidation.
Aromatic amines have historical applications in the field of photography.

They were used in the formulation of certain photographic chemicals and processes.
Some aromatic amines are investigated for their potential use as corrosion inhibitors.
They may be employed to protect metals from corrosion in certain industrial applications.

Aromatic amines, including certain derivatives, have been used as color developers in the photographic industry, contributing to the formation of color images.
Aromatic amines may be used as auxiliaries in the textile industry for processes such as dyeing and finishing.
N,N-Dimethyl-p-toluidine (DMPT) is an amine accelerator for the polymerization of e.g. dental methacrylic restorative materials.

N,N-Dimethyl-p-toluidine (DMPT) is used as a polymerization catalyst for polyesters, acrylate and epoxy resins.
N,N-Dimethyl-p-toluidine (DMPT) is also used as a hardener for dental cements and in adhesives.
N,N-Dimethyl-p-toluidine (DMPT) serves as an intermediate for photographic chemicals, in industrial glues, in artificial fingernail preparations, colorants, pharmaceuticals.

N,N-Dimethyl-p-toluidine (DMPT) reacts with vinyl ether in the presence of copper(II) chloride gives tetrahydroquinolines.
Further, N,N-Dimethyl-p-toluidine (DMPT) is used to accelerate polymerization of ethyl methacrylate.
Aromatic amines, including N,N-Dimethyl-p-toluidine (DMPT), are important intermediates in the synthesis of azo dyes.

These dyes are widely used in the textile industry for coloring fabrics.
Aromatic amines can be used as intermediates in the synthesis of pharmaceutical compounds.
They may play a role in the creation of specific drug molecules or building blocks.

N,N-Dimethyl-p-toluidine (DMPT), like other aromatic amines, can participate in various chemical reactions, making it valuable in the synthesis of diverse organic compounds.
Some aromatic amines exhibit catalytic properties and may be employed in catalytic processes.

Health Hazard:
Inhalation, ingestion or skin contact with material may cause severe injury or death.
Contact with molten N,N-Dimethyl-p-toluidine (DMPT) may cause severe burns to skin and eyes.
Avoid any skin contact.

Fire Hazard:
Combustible material: may burn but does not ignite readily.
When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards.
Contact with metals may evolve flammable hydrogen gas.

Safety Profile:
Prolonged or repeated exposure to these compounds may increase the risk of developing cancer.
Certain aromatic amines are mutagenic, meaning they have the potential to cause genetic mutations.
Mutations can lead to various health issues, including cancer.

Aromatic amines can be toxic, and exposure to them may cause adverse health effects.
The specific toxicity can vary among different aromatic amines and depends on factors such as chemical structure, concentration, and duration of exposure.
Aromatic amines may cause irritation to the skin and eyes upon contact.

Skin exposure can lead to dermatitis, and eye exposure may result in irritation or damage.
Some aromatic amines are known or suspected carcinogens, meaning they have the potential to cause cancer.
Inhalation of vapors or dust containing aromatic amines may irritate the respiratory system, leading to symptoms such as coughing, difficulty breathing, or irritation of the nose and throat.

N,N'-Dimethylurea, an alkyl urea derivative, is a nonlinear organic material.
N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N'-Dimethylurea forms needle-shaped crystals.


CAS Number: 96-31-1
EC Number: 202-498-7
MDL number: MFCD00008286
Linear Formula: (CH3NH)2CO
Chemical formula: C3H8N2O



SYNONYMS:
1,3-Dimethylurea, sym-dimethylurea, N,N-Dimethylurea, n,n'-dimethyl-ure, N,N'-dimethylurea, Dimethyl Urea 1,3, symmetricdimethylurea, symmetric dimethylurea, n,n'-dimethylharnstoff, Symmetric dimethylurea, N,N'-Dimethylharnstoff, N,N-dimethylurea (sym.), 1,3-Dimethylurea Factory, N,N'-Dimethylurea Factory, 1,3-Dimethylurea COA TDS MSDS, 1,3-DIMETHYLUREA, N,N'-Dimethylurea, 96-31-1, sym-Dimethylurea, Urea, N,N'-dimethyl-, Symmetric dimethylurea, Urea, 1,3-dimethyl-, 1,3-Dimethyl urea, N,N'-Dimethylharnstoff, dimethyl urea, NSC 14910, BRN 1740672, AI3-24386, MFCD00008286, WAM6DR9I4X, DTXSID5025156, CHEBI:80472, Urea,3-dimethyl-, Urea,N'-dimethyl-, NSC-14910, 1,3-Dimethylurea, 98%, WLN: 1MVM1, CCRIS 2509, HSDB 3423, EINECS 202-498-7, UNII-WAM6DR9I4X, Dimethylharnstoff, 1.3-Dimethylurea, N,N-Dimethyl-Urea, 1,3 dimethyl urea, N,N'-dimethyl urea, N,N'-dimethylurea, 1,1'-Dimethylurea, 1,3-Dimethylcarbamide, 3k3g, bmse000248, EC 202-498-7, UREA,1,3-DIMETHYL, (CH3NH)2CO, DIMETHYL UREA [INCI], DIMETHYLUREA, N,N'-, N,N'-Dimethylurea, ~98%, DTXCID605156, CHEMBL1234380, 1,3-DIMETHYLUREA [HSDB], NSC14910, NSC24823, Tox21_200794, 1,3-Dimethylurea;N,N'-Dimethylurea, BBL011513, NSC-24823, STL146629, AKOS000120912, CS-W013749, PB47928, CAS-96-31-1, NCGC00248834-01, NCGC00258348-01, SY004507, DB-225923, N,N inverted exclamation mark-Dimethylurea, N,N inverted exclamation marka-Dimethylurea, A4569, D0289, NS00005754, EN300-20740, P17517, ethyl 5-oxo-2,3-diphenyl-cyclopentanecarboxylate, A845576, N,N'-Dimethylurea, (sym.), >=99% (from N), Q419740, W-100145, N,N'-Dimethylurea, PESTANAL(R), analytical standard, F0001-2292, N,N'-Dimethylurea, (sym.), >=95.0% (HPLC), technical, InChI=1/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6, DMU, 1,3-Dimethylurea, N,N′-Dimethylurea, Urea,N,N’-dimethyl,UNII-, AM6DR9I4X, MeNHNCONHMe, sym-Dimethylurea,N,N`-Dimethylurea, Expand DMU, N,N'-Dimethylharnstoff [German], N,N'-Dimethylurea, Symmetric dimethylurea, sym-Dimethylurea, Urea, 1,3-dimethyl-, Urea, N,N'-dimethyl-, N,N′-Dimethylurea, DMU, 1,3-Dimethylurea, 1,3-DIMETHYLUREA, N,N'-Dimethylurea, 96-31-1, sym-Dimethylurea, Urea, N,N'-dimethyl-, Symmetric dimethylurea, Urea, 1,3-dimethyl-, N,N'-Dimethylharnstoff, 1,3-Dimethyl urea, NSC 14910, BRN 1740672, AI3-24386, MFCD00008286, WAM6DR9I4X, DMU, DTXSID5025156, CHEBI:80472, Urea,3-dimethyl-, Urea,N'-dimethyl-, NSC-14910, 1,3-Dimethylurea, 98%, WLN: 1MVM1, CCRIS 2509, HSDB 3423, EINECS 202-498-7, UNII-WAM6DR9I4X, Dimethylharnstoff, 1.3-Dimethylurea, N,N-Dimethyl-Urea, 1,3 dimethyl urea, N,N'-dimethyl urea, 1,1'-Dimethylurea, 1,3-Dimethylcarbamide, bmse000248, EC 202-498-7, UREA,1,3-DIMETHYL, (CH3NH)2CO, DIMETHYL UREA [INCI], DIMETHYLUREA, N,N'-, N,N'-Dimethylurea, ~98%, DTXCID605156, CHEMBL1234380, 1,3-DIMETHYLUREA [HSDB], NSC14910, NSC24823, Tox21_200794, 1,3-Dimethylurea;N,N'-Dimethylurea, NSC-24823, AKOS000120912, CS-W013749, PB47928, CAS-96-31-1, NCGC00248834-01, NCGC00258348-01, SY004507, N,N inverted exclamation mark -Dimethylurea, A4569, D0289, FT-0606700, EN300-20740, P17517, ethyl 5-oxo-2,3-diphenyl cyclopentanecarboxylate, A845576, N,N'-Dimethylurea, (sym.), >=99% (from N), Q419740, W-100145, N,N'-Dimethylurea, PESTANAL(R), analytical standard, F0001-2292, N,N'-Dimethylurea, (sym.), >=95.0% (HPLC), technical, InChI=1/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6), Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N' Dimethylharnstoff, NSC 14910, (CH3NH)2CO, 1,1'-Dimethylurea, 1,3-dimethylurea, DMU, N,N'-Dimethylharnstoff, N,N'-dimethylurea, NSC 14910, Symmetric dimethylurea, sym-Dimethylurea, urea, 1,3-dimethyl-, syM,N,N'-DIMETHYLUREA, (CH3NH)2CO, AKOS B029718, 1.3-DiMethyl u, 1,3-dimethyl-ure, SYM-DIMETHYLUREA, 1,3-DIMETHYLUREA, n,n’-dimethyl-ure,Dimethylcarbamide, N,N'-Dimethyl urea, 1,3-Dimethylurea, N,N’-dimethyl-Urea, 1,3-dimethyl-ure, n,n’-dimethylharnstoff, n,n’-dimethylharnstoff (german), n,n’-dimethylurea, sym-dimethylurea, Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N'-Dimethylharnstoff, NSC 14910, Urea, N,N′-dimethyl-, Urea, 1,3-dimethyl-, N,N′-Dimethylurea, 1,3-Dimethylurea, Symmetric dimethylurea, sym-Dimethylurea, NSC 14910, NSC 24823, Urea,1,3-dimethyl- (8CI), N,N'-Dimethylurea, NSC 14910, NSC 24823, Symmetric dimethylurea, sym-Dimethylurea, Urea,N,N’-dimethyl, UNII-WAM6DR9I4X, MeNHNCONHMe, sym-Dimethylurea, N,N`-Dimethylurea, syM, N,N'-DIMETHYLUREA, (CH3NH)2CO, AKOS B029718, 1.3-DiMethyl u, 1,3-dimethyl-ure, SYM-DIMETHYLUREA, 1,3-DIMETHYLUREA, n,n’-dimethyl-ure, Dimethylcarbamide, n,n’-dimethylurea, sym-dimethylurea, urea, n,n’-dimethyl, dimethylurea, symmetric dimethylurea, urea, 1,3-dimethyl, n,n’-dimethylharnstoff, 1,3-dimethyl urea, n,n’-dimethylharnstoff german, unii-wam6dr9i4x, Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N'-Dimethylharnstoff, NSC 14910, Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N'-Dimethylharnstoff, NSC 14910, 1,1-DIMETHYLUREA, 598-94-7, N,N-Dimethylurea, Urea, N,N-dimethyl-, asym-Dimethylurea, Urea, 1,1-dimethyl-, 1320-50-9, 1,1-DIMETHYL-D6-UREA, 1.1-Dimethylurea, MFCD00007959, 1219802-32-0, NSC-33603, I988R763P3, 1,1-Dimethyl urea, N,N-Dimethylharnstoff, N,N-Dimethylharnstoff [German], HSDB 4273, EINECS 209-957-0, NSC 33603, BRN 1740666, AI3-61297, UNII-I988R763P3, N,N-dimethyl urea, EINECS 215-303-5, 1,1-dimethyl-urea, DIMETHYLUREA, N,N-, 1,1-Dimethylurea, 99%, (CH3)2NCONH2, DTXSID0060515, 1,1-DIMETHYLUREA [HSDB], NSC33603, STR03134, STL482999, AKOS000200400, SY048169, DB-053491, CS-0132397, D0809, NS00021239, EN300-17007, D-5580, D89723, A832531, Q24712449, InChI=1/C3H8N2O/c1-5(2)3(4)6/h1-2H3,(H2,4,6, n,n'-dimethylurea, sym-dimethylurea, urea, n,n'-dimethyl, dimethylurea, symmetric dimethylurea, urea, 1,3-dimethyl, n,n'-dimethylharnstoff, 1,3-dimethyl urea, n,n'-dimethylharnstoff german, unii-wam6dr9i4x



N,N'-Dimethylurea, an alkyl urea derivative, is a nonlinear organic material.
N,N’-Dimethylurea is soluble in water.
N,N’-Dimethylurea acts as a radical scavenger that protects isolated pancreatic islets from the effects of alloxan and dihydroxyfumarate exposure.
Methyl amine and N,N’-Dimethylurea are hydrolysis products of methyl isocyanate.


N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.
N,N'-Dimethylurea forms needle-shaped crystals.


N,N'-Dimethylurea has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique.
N,N'-Dimethylurea's crystals has one molecule in each asymmetric unit.
N,N’-Dimethylurea 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.


N,N’-Dimethylurea is an organic compound that has been shown to bind to the carbonyl group of proteins and act as a hydrogen-bond donor.
The nitrogen atoms are coordinated to form two pyramidal structures with the hydrogen bonding between the nitrogen atoms.
This coordination geometry leads to a molecule that is planar and the frequency shift of IR spectroscopy data confirms this structure.


The reaction mechanism for dimethyl urea begins with an attack by the oxygen atom on the carbon atom of tetramethylurea forming an intermediate called trimethylamine, which then reacts with trifluoroacetic acid (TFA) leading to the formation of dimethyl urea.
N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.


Molecules in crystal are linked by hydrogen bonds.
N,N'-Dimethylurea is a colorless powder, used as building block for active ingredients or intermediate for formaldehyde-free textile additives.
N,N’-Dimethylurea is a white crystals


N,N’-Dimethylurea is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.
N,N’-Dimethylurea is a colorless crystals.
N,N’-Dimethylurea is water soluble.


N,N'-Dimethylurea is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.
N,N’-Dimethylurea is a colorless solid.
N,N’-Dimethylurea is a colorless powder.


N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.
N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.


N,N’-Dimethylurea is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.
N,N’-Dimethylurea is a solid in the form of white crystals with a faint ammonia-like odor.
N,N’-Dimethylurea is soluble in water.


N,N’-Dimethylurea is a colorless, volatile liquid with a penetrating odor.
N,N’-Dimethylurea is soluble in water and alcohols and has a melting point of -3°C.
N,N’-Dimethylurea is a solid in the form of white crystals with a faint ammonia-like odor.


N,N’-Dimethylurea is a urea derivative used as an intermediate in organic synthesis.
N,N’-Dimethylurea appears as colorless crystals and is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3 .
N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.


N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.
N,N’-Dimethylurea appears as colorless crystals.
N,N’-Dimethylurea is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.



USES and APPLICATIONS of N,N'-DIMETHYLUREA:
Typical applications of N,N'-Dimethylurea: Agriculture, Urea-herbicide, Carbamate-herbicide, and Textile additives.
N,N’-Dimethylurea is used for the manufacture of: chemicals.
Release to the environment of N,N’-Dimethylurea can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), in processing aids at industrial sites and as processing aid.


N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N’-Dimethylurea is a colorless crystalline powder with little toxicity.
N,N’-Dimethylurea is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.


N,N'-Dimethylurea is used Formaldehyde-free textile additives.
N,N'-Dimethylurea is used cross linking agent for textiles made of cellulose fibers and their synthetic mixtures.
N,N'-Dimethylurea has used Pharmaceuticals.


In the textile processing industry N,N’-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.
In the Swiss Product Register there are 38 products containing N,N’-Dimethylurea, among them 17 products intended for consumer use.


Product types of N,N’-Dimethylurea are e.g. paints and cleaning agents.
The content of N,N’-Dimethylurea in consumer products is up to 10 %.
Use in cosmetics of N,N’-Dimethylurea has been proposed, but there is no information available as to its actual use in such applications.


N,N’-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.
N,N’-Dimethylurea is used in the following areas: health services and scientific research and development.
Other release to the environment of N,N’-Dimethylurea is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).


Release to the environment of N,N’-Dimethylurea can occur from industrial use: formulation of mixtures.
N,N’-Dimethylurea is used in the following products: pH regulators and water treatment products and laboratory chemicals.
N,N’-Dimethylurea is used in the following areas: health services and scientific research and development.


N,N’-Dimethylurea is used as textile auxiliaries to produce formaldehyde-free anti-wrinkle finishing products.
N,N’-Dimethylurea is used in cosmetics as an emollient.
N,N’-Dimethylurea is used in medicine and can produce a variety of raw materials.


N,N'-Dimethylurea is a used reagant for the synthesis of active ingredients, such as bronchodilators.
N,N'-Dimethylurea can be used as a starting material to synthesize N,N'-dimethyl-6-amino uracil.
N,N’-Dimethylurea is used in chemical industry, it can synthesize a variety of chemical products.


N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N’-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.
N,N’-Dimethylurea is used in the textile processing industry.


Pharmaceutical intermediates, N,N’-Dimethylurea is also used in the production of fiber treatment agents.
In medicine, N,N’-Dimethylurea is used to synthesize theophylline, caffeine and nifedipine hydrochloride, etc.
N,N’-Dimethylurea is used by professional workers (widespread uses), in formulation or re-packing and at industrial sites.


N,N’-Dimethylurea is used in the following products: pH regulators and water treatment products and laboratory chemicals.
N,N'-Dimethylurea is used in combination with ß-cyclodextrin derivatives, to form low melting mixtures (LMMs), which can be used as solvents for hydroformylation and Tsuji-Trost reactions.


N,N'-Dimethylurea is used to synthesize N,N'-disubstituted-4-aryl-3,4-dihydropyrimidinones via Biginelli condensation under solvent-free conditions.
N,N'-Dimethylurea is the suitable reagent used to investigate the polar structure of its crystals.
N,N’-Dimethylurea is used as a catalyst for condensation of methylamine with urea.


N,N’-Dimethylurea is used as a pharmaceutical drug to treat hyperammonemia.
N,N’-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.
N,N’-Dimethylurea is used in pharmaceutical manufacturing.


N,N’-Dimethylurea is used as an intermediate to make caffeine, pharmachemicals, textile aids, herbicides, paints, and cleaning products.
N,N’-Dimethylurea is used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.
In the textile processing industry N,N’-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.


N,N’-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.
In the textile processing industry N,N’-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.


The estimated world production of N,N’-Dimethylurea is estimated to be less than 25,000 tons.
N,N'-Dimethylurea may be used in the Dowex-50W ion exchange resin-promoted solvent-free synthesis of N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones.
N,N'-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.


N,N’-Dimethylurea is used in the textile processing industry.
N,N’-Dimethylurea is used as an intermediate in organic synthesis. 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.


N,N’-Dimethylurea is used as an intermediate in the synthesis of theophylline and caffeine, and also used in the production of fiber treatment agents
N,N’-Dimethylurea is used in manufacturing synthetic caffeine, resins and drugs.
In the textile processing industry N,N'-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.


-N,N’-Dimethylurea can be used as a starting material to synthesize N,N′-dimethyl-6-amino uracil.
In combination with β-cyclodextrin derivatives, to form low melting mixtures (LMMs), which can be used as solvents for hydroformylation and Tsuji-Trost reactions.
To synthesize N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones via Biginelli condensation under solvent-free conditions.



PURIFICATION METHODS OF N,N'-DIMETHYLUREA:
Crystallise the urea from acetone/diethyl ether by cooling in an ice bath.
Also crystallise N,N’-Dimethylurea from EtOH and dry it at 50o/5mm for 24hours



FEATURES OF N,N'-DIMETHYLUREA:
*Good stability
N,N’-Dimethylurea has good stability and are suitable for various synthetic chemical reactions, ensuring the stability and reliability of our customers' production processes.



MOLECULAR STRUCTURE ANALYSIS OF N,N'-DIMETHYLUREA:
N,N’-Dimethylurea forms needle-shaped crystals .
The Raman spectra of DMU crystal have been measured, and the density function theory with a B3LYP/6-311G* * basis set has been used to optimize the geometry structure and calculate the vibrational frequency of gas phase DMU .



CHEMICAL REACTIONS ANALYSIS OF N,N'-DIMETHYLUREA:
The reaction of N,N’-Dimethylurea with formaldehyde has been studied in detail using quantitative on-line NMR spectroscopy.
The system undergoes only four reactions and, unlike urea–formaldehyde, does not form polymers .



SYNTHESIS ANALYSIS OF N,N'-DIMETHYLUREA:
A practically simple, mild, and efficient method has been developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without an organic co-solvent.



PRODUCTION METHOD OF N,N'-DIMETHYLUREA:
Industry uses molten urea and monomethyl amine action to make. First, the area into the melting tank, heated to 130-135C to melt N,N’-Dimethylurea, transferred to the reaction tower has been heated to 110-120C, continue to raise the temperature to 150-175 ℃, began to pass the purified monomethyl amine gas, until the monomethyl amine all through, that is, the reaction is completed, the creation of even dimethyl urea finished products.



REACTIVITY PROFILE OF N,N'-DIMETHYLUREA:
N,N’-Dimethylurea is an amide.
Amides are very weak bases (weaker than water).
Imides are less basic yet and in fact react with strong bases to form salts.

That is, they can react as acids.
Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile.
The combustion of these compounds generates mixed oxides of nitrogen (NOx).



PHYSICAL AND CHEMICAL PROPERTIES ANALYSIS OF N,N'-DIMETHYLUREA:
N,N’-Dimethylurea is a colorless crystalline powder with little toxicity .
The effects of concentration variation of 1,3-DMU in distilled water on dielectric and electrical properties have been discussed to gain information about the self-aggregative nature of N,N’-Dimethylurea and dissociation process in aqueous solutions



PHYSICAL AND CHEMICAL PROPERTIES OF N,N'-DIMETHYLUREA:
Character: gray-white, thin, thin, crystalline.
melting point 101~104 ℃
boiling point 268~270 ℃
relative density 1.142
solubility in water, ethanol, acetone, benzene and ethyl acetate, insoluble in ether and gasoline.



PHYSICAL and CHEMICAL PROPERTIES of N,N'-DIMETHYLUREA:
Physical state: flakes
Color: colorless
Odor: amine-like
Melting point/freezing point:
Melting point/range: 103 - 106 °C
Initial boiling point and boiling range: 268 - 270 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 157 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 9,0 - 9,5

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 765 g/l at 21,5 °C - soluble
Partition coefficient:
n-octanol/water: log Pow: -0,783
Vapor pressure: No data available
Density: 1,14 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: No data available
Other safety information:
Bulk density 0,50 g/l
Molecular Formula: CH3NHCONHCH3
CAS No: 96-31-1
EINECS: 202-498-7
Molecular Weight: 88.11
Appearance: White Crystals
Assay: ≥ 95%
Freezing point: 103'C Min
Volatile Content: ≤ 0.2%
Melting point: 104'C
CAS number: 96-31-1
EC number: 202-498-7
Hill Formula: C₃H₈N₂O

Molecular Weight: 88.11
Molecular Formula: C3H8N2O
Canonical SMILES: CNC(=O)NC
InChI: InChI=1S/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6)
InChIKey: MGJKQDOBUOMPEZ-UHFFFAOYSA-N
Chemical formula: C3H8N2O
Molar mass: 88.110 g·mol−1
Appearance: Colorless, waxy crystals
Odor: Odorless
Density: 1.142 g mL−1
Melting point: 104.4 °C; 219.8 °F; 377.5 K
Boiling point: 269.1 °C; 516.3 °F; 542.2 K
Solubility in water: 765 g L−1
Magnetic susceptibility (χ): -55.1·10−6 cm3/mol

Thermochemistry:
Std enthalpy of formation (ΔfH⦵298): −312.1–−312.1 kJ mol−1
Std enthalpy of combustion (ΔcH⦵298): −2.0145–−2.0089 MJ mol−1
Additional Properties:
Molecular Weight: 88.11 g/mol
XLogP3: -0.5
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 88.063662883 g/mol
Monoisotopic Mass: 88.063662883 g/mol
Topological Polar Surface Area: 41.1Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 46.8

Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Appearance: Colorless crystals (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 108.00 °C. @ 760.00 mm Hg
Boiling Point: 269.00 °C. @ 760.00 mm Hg

Vapor Pressure: 0.547000 mmHg (est)
Flash Point: 116.00 °F. TCC (46.60 °C.) (est)
logP (o/w): -0.490
Soluble in water: 1.615e+004 mg/L @ 25 °C (est)
Chemical formula: C3H8N2O
Molar mass: 88.110 g·mol−1
Appearance: Colorless, waxy crystals
Odor: Odorless
Density: 1.142 g mL−1
Melting point: 104.4 °C; 219.8 °F; 377.5 K
Boiling point: 269.1 °C; 516.3 °F; 542.2 K

Solubility in water: 765 g L−1
Magnetic susceptibility (χ): -55.1·10−6 cm3/mol
Thermochemistry:
Std enthalpy of formation (ΔfH⦵298): −312.1–−312.1 kJ mol−1
Std enthalpy of combustion (ΔcH⦵298): −2.0145–−2.0089 MJ mol−1
Molecular Weight: 88.11 g/mol
XLogP3: -0.5
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 88.063662883 g/mol
Monoisotopic Mass: 88.063662883 g/mol

Topological Polar Surface Area: 41.1Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 46.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Boiling Point: 268-270 ℃
Melting Point: 101-105 ℃
Flash Point: 157ºC
Purity: > 98.0 % (GC)
Density: 1.142 g/cm3
Appearance: Colorless crystals.
Storage: Store at RT.
HS Code: 29241900
Log P: 0.32700
MDL: MFCD00008286
PSA: 41.13
Refractive Index: 1.413
Risk Statements: R62

RTECS: YS9868000
Safety Statements: S24/25
Stability: Stable under normal temperatures and pressures.
SYNONYMS: N,N′-Dimethylurea
CAS NUMBER: 96-31-1
MOLECULAR WEIGHT: 88.11
BEILSTEIN REGISTRY NUMBER: 1740672
EC NUMBER: 202-498-7
MDL NUMBER: MFCD00008286
Auto Ignition: 400 °C (DIN 51794) (Lit.)
Base Catalog Number: 15784780
Beilstein Registry Number: 1740672
Boiling Point: 262 °C (Lit.)
CAS #: 96-31-1
Density: 1.14 g/cm3 at 20 °C (Lit.)

EC Number: 202-498-7
Flash Point: > 157 °C (Lit.)
Melting Point: 100 - 110 °C
Molecular Formula: C3H8N2O
Molecular Weight: 88.11
pH: 9.0 - 9.5 (100 g/L, H2O, 20 °C) (Lit.)
Purity: ≥98%
RTECS Number: YS9868000
Solubility: Soluble in ethanol (200 mg in 4 mL).
Melting Point: 105°C
Boiling Point: 270°C
Color: White
Formula Weight: 88.11
Physical Form: Crystal-Powder at 20°C
Chemical Name or Material: 1,3-Dimethylurea
CAS: 96-31-1

EINECS: 202-498-7
InChI: InChI=1/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6)
InChIKey: MGJKQDOBUOMPEZ-UHFFFAOYSA-N
Molecular Formula: C3H8N2O
Molar Mass: 88.11
Density: 1.142
Melting Point: 101-104°C (lit.)
Boiling Point: 268-270°C (lit.)
Flash Point: 157 °C
Water Solubility: 765 g/L (21.5 ºC)
Solubility: Soluble in water, ethanol, acetone, benzene, and ethyl acetate, etc.,
insoluble in ether and gasoline.
Vapor Pressure: 6 hPa (115 °C)
Appearance: Crystallization
Color: White

BRN: 1740672
pKa: 14.57±0.46 (Predicted)
pH: 9.0-9.5 (100g/l, H2O, 20℃)
Storage Condition: Store below +30°C.
Refractive Index: 1.4715 (estimate)
MDL: MFCD00008286
Melting Point: 100°C to 104°C
Density: 1.14
Boiling Point: 268°C to 270°C (decomposition)
Flash Point: 157°C (314°F)
Quantity: 250 g
Beilstein: 1740672
Formula Weight: 88.11
Percent Purity: 98%

Chemical Name or Material: N,N'-Dimethylurea
Chemical formula: CH₃NHCONHCH₃
Molar Mass: 88.11 g/mol
HS Code: 2924 19 00
Boiling point: 268 - 270 °C (1013 hPa)
Density: 1.14 g/cm3 (20 °C)
Flash point: 157 °C DIN 51758
Ignition temperature: 400 °C
Melting Point: 101 - 104 °C
pH value: 9.0 - 9.5 (H₂O)
Vapor pressure: <0.1 hPa (20 °C)
Bulk density: 500 kg/m3
Solubility: 765 g/l

Chemical Name: N,N’-dimethylurea
CAS No.: 96-31-1
Molecular Formula: C3H8N2O
Molecular Weight: 88.10840
PSA: 41.13000
LogP: 0.32700
Appearance & Physical State: white flake
Density: 1.142
Boiling Point: 268-270ºC
Melting Point: 101-105ºC
Flash Point: 157ºC
Refractive Index: 1.413
Water Solubility: 765 g/L (21.5 ºC)

Stability: Stable under normal temperatures and pressures.
Storage Condition: Store at RT.
Melting point: 101-104 °C(lit.)
Boiling point: 268-270 °C(lit.)
Density: 1.142
vapor pressure: 6 hPa (115 °C)
refractive index: 1.4715 (estimate)
Flash point: 157 °C
storage temp.: Store below +30°C.
solubility: H2O: 0.1 g/mL, clear, colorless

pka: 14.57±0.46(Predicted)
form: Crystals
color: White
PH: 9.0-9.5 (100g/l, H2O, 20℃)
Water Solubility: 765 g/L (21.5 ºC)
BRN: 1740672
InChIKey: MGJKQDOBUOMPEZ-UHFFFAOYSA-N
LogP: -0.783 at 25℃
CAS DataBase Reference: 96-31-1(CAS DataBase Reference)
FDA UNII: WAM6DR9I4X
NIST Chemistry Reference: Urea, N,N'-dimethyl-(96-31-1)
EPA Substance Registry System: 1,3-Dimethylurea (96-31-1)

CAS No.: 96-31-1
Molecular Formula: C3H8N2O
InChIKeys: InChIKey=MGJKQDOBUOMPEZ-UHFFFAOYSA-N
Molecular Weight: 88.11
Exact Mass: 88.11
EC Number: 202-498-7
UNII: WAM6DR9I4X
ICSC Number: 1745
NSC Number: 24823|14910
DSSTox ID: DTXSID5025156
Color/Form: RHOMBIC BIPYRAMIDAL CRYSTALS FROM CHLOROFORM-ETHER|COLORLESS PRISMS
HScode: 2924199090

PSA: 41.1
XLogP3: -0.5
Appearance: N,n'-dimethylurea appears as colorless crystals. (NTP, 1992)
Density: 1.142 g/cm3
Melting Point: 108 °C
Boiling Point: 268-270 °C
Flash Point: 154°C
Refractive Index: 1.414
Water Solubility: H2O: 765 g/L (21.5 ºC)
Vapor Pressure: Vapour pressure, Pa at 20°C: 0.042
Air and Water Reactions: Water soluble.
Reactive Group: Amides and Imides

Autoignition Temperature: 400 °C
Molecular Formula / Molecular Weight: C3H8N2O = 88.11
Physical State (20 deg.C): Solid
CAS RN: 96-31-1
Reaxys Registry Number: 1740672
PubChem Substance ID: 87566985
SDBS (AIST Spectral DB): 2161
MDL Number: MFCD00008286
Appearance: colorless crystals (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 108.00 °C. @ 760.00 mm Hg
Boiling Point: 269.00 °C. @ 760.00 mm Hg

Vapor Pressure: 0.547000 mmHg (est)
Flash Point: 116.00 °F. TCC ( 46.60 °C. ) (est)
logP (o/w): -0.490
Soluble in: water, 1.615e+004 mg/L @ 25 °C (est)
Synonyms: N,N'-Dimethylurea
Molecular Formula: C3H8N2O
Molecular Weight: 88.11
CAS Number: 96-31-1
EINECS: 202-498-7
Appearance: White powder
Density: 1.142
Melting Point: 101-105 ºC
Stability: Stable under ordinary conditions.
Appearance: White powder
PH value: 6.5-8.0

Assay: ≥97.5%
Water: ≤0.5
Density: 0.9±0.1 g/cm3
Boiling Point: 269.0±0.0 °C at 760 mmHg
Melting Point: 101-104 °C(lit.)
Molecular Formula: C3H8N2O
Molecular Weight: 88.108
Flash Point: 124.3±18.9 °C
Exact Mass: 88.063660
PSA: 41.13000
LogP: -1.01
Vapour Pressure: 0.0±0.5 mmHg at 25°C
Index of Refraction: 1.414
Storage condition: Store at RT.
Water Solubility: 765 g/L (21.5 ºC)
Synonyms: 1,3-dimethylurea



FIRST AID MEASURES of N,N'-DIMETHYLUREA:
-Description of first-aid measures:
*General advice:
Consult a physician.
Show this material 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:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N'-DIMETHYLUREA:
-Environmental precautions:
Do not let product 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.



FIRE FIGHTING MEASURES of N,N'-DIMETHYLUREA:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of N,N'-DIMETHYLUREA:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
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:
Choose body protection
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N'-DIMETHYLUREA:
-Precautions for safe handling:
*Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of N,N'-DIMETHYLUREA:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

N,N-Dimethylurea (DMU) is an organic chemical substance, CAS No.:96-31-1, molecular formula: C3H8N2O
N,N-Dimethylurea (DMU) is a colorless, volatile liquid with a penetrating odor.


CAS Number: 96-31-1
EC Number: 202-498-7
MDL number: MFCD00008286
Linear Formula: (CH3NH)2CO
Chemical formula: C3H8N2O



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F0001-2292, N,N'-Dimethylurea, (sym.), >=95.0% (HPLC), technical, InChI=1/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6), Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N' Dimethylharnstoff, NSC 14910, (CH3NH)2CO, 1,1'-Dimethylurea, 1,3-dimethylurea, DMU, N,N'-Dimethylharnstoff, N,N'-dimethylurea, NSC 14910, Symmetric dimethylurea, sym-Dimethylurea, urea, 1,3-dimethyl-,
syM,N,N'-DIMETHYLUREA, (CH3NH)2CO, AKOS B029718, 1.3-DiMethyl u, 1,3-dimethyl-ure, SYM-DIMETHYLUREA, 1,3-DIMETHYLUREA, n,n’-dimethyl-ure,Dimethylcarbamide
N,N'-Dimethyl urea, 1,3-Dimethylurea, N,N’-dimethyl-Urea, 1,3-dimethyl-ure, n,n’-dimethylharnstoff, n,n’-dimethylharnstoff (german), n,n’-dimethylurea, sym-dimethylurea, Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N'-Dimethylharnstoff, NSC 14910, Urea, N,N′-dimethyl-, Urea, 1,3-dimethyl-, N,N′-Dimethylurea, 1,3-Dimethylurea, Symmetric dimethylurea, sym-Dimethylurea,
NSC 14910, NSC 24823, Urea,1,3-dimethyl- (8CI), N,N'-Dimethylurea, NSC 14910, NSC 24823, Symmetric dimethylurea, sym-Dimethylurea, Urea,N,N’-dimethyl, UNII-WAM6DR9I4X, MeNHNCONHMe, sym-Dimethylurea, N,N`-Dimethylurea,



N,N-Dimethylurea (DMU) is a urea derivative and used as an intermediate in organic synthesis.
N,N-Dimethylurea (DMU) is a colorless crystalline powder with little toxicity.
N,N-Dimethylurea (DMU) is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.


In the textile processing industry N,N-Dimethylurea (DMU) is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.
In the Swiss Product Register there are 38 products containing N,N-Dimethylurea (DMU), among them 17 products intended for consumer use.


Product types are e.g. paints and cleaning agents.
The content of N,N-Dimethylurea (DMU) in consumer products is up to 10 %.
Use in cosmetics has been proposed, but there is no information available as to N,N-Dimethylurea (DMU)'s actual use in such applications.


N,N-Dimethylurea (DMU) is a white crystals.
N,N-Dimethylurea (DMU) is a colorless, volatile liquid with a penetrating odor.
N,N-Dimethylurea (DMU) is soluble in water and alcohols and has a melting point of -3°C.


N,N-Dimethylurea (DMU) is a colorless powder, used as building block for active ingredients or intermediate for formaldehyde-free textile additives.
N,N-Dimethylurea (DMU) is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.
N,N-Dimethylurea (DMU) is water soluble.


N,N-Dimethylurea (DMU) is an organic compound that has been shown to bind to the carbonyl group of proteins and act as a hydrogen-bond donor.
The nitrogen atoms are coordinated to form two pyramidal structures with the hydrogen bonding between the nitrogen atoms.
This coordination geometry leads to a molecule that is planar and the frequency shift of IR spectroscopy data confirms this structure.


The reaction mechanism for N,N-Dimethylurea (DMU) begins with an attack by the oxygen atom on the carbon atom of tetramethylurea forming an intermediate called trimethylamine, which then reacts with trifluoroacetic acid (TFA) leading to the formation of N,N-Dimethylurea (DMU).
N,N-Dimethylurea (DMU) is a colorless crystals.


N,N-Dimethylurea (DMU) Market revolves around the production and distribution of the chemical compound 1,3-Dimethylurea, identified by the CAS (Chemical Abstracts Service) number 96–31–1.
N,N-Dimethylurea (DMU) is a derivative of urea and is characterized by its molecular structure, consisting of two methyl groups attached to the nitrogen atoms of the urea molecule.


N,N-Dimethylurea (DMU) Market plays a crucial role in the chemical industry, serving as a key intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals.
N,N-Dimethylurea (DMU) is utilized as a building block in the creation of complex molecules, contributing to advancements in drug development and agricultural formulations.


The growth of the N,N-Dimethylurea (DMU) Market is propelled by several key factors.
Primarily, the compound’s significance as an intermediate in the synthesis of pharmaceuticals drives its demand, as N,N-Dimethylurea (DMU) plays a crucial role in the development of diverse drug compounds.



USES and APPLICATIONS of N,N-DIMETHYLUREA (DMU):
N,N-Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis.
N,N-Dimethylurea (DMU) is with the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives.


One such N,N-Dimethylurea (DMU) is Salicylaldehyde which has developed particularly rapidly in recent years.
Pharmaceutical intermediates, N,N-Dimethylurea (DMU) is also used in the production of fiber treatment agents.
In medicine, N,N-Dimethylurea (DMU) is used to synthesize theophylline, caffeine and nifedipine hydrochloride, etc.


The design, research, and development of pharmaceutical intermediates of N,N-Dimethylurea (DMU) including more than 330 kinds of pharmaceutical intermediates such as Anti-infectives, Cardiovascular and Cerebrovascular Systems, Digestive System, Santi-tumor, Nervous System, Geriatric Drugs, and Gynecological Drugs.


N,N-Dimethylurea (DMU) is used as a starting material to synthesize N,N′-dimethyl-6-amino uracil.
N,N-Dimethylurea (DMU) is used in combination with β-cyclodextrin derivatives, to form low melting mixtures (LMMs), which can be used as solvents for hydroformylation and Tsuji-Trost reactions.


N,N-Dimethylurea (DMU) is used to synthesize N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones via Biginelli condensation under solvent-free conditions.
N,N-Dimethylurea (DMU) is intermediate used in the production of and Agrochemical.
N,N-Dimethylurea (DMU) is used Agriculture, Urea-herbicide, Carbamate-herbicide, and Textile additives.


N,N-Dimethylurea (DMU) is used Formaldehyde-free textile additives, Cross linking agent for textiles made of cellulose fibers and their, synthetic mixtures, and Pharmaceuticals.
N,N-Dimethylurea (DMU) is used reagant for the synthesis of active ingredients, such as bronchodilators.


N,N-Dimethylurea (DMU) is used as a pharmaceutical drug to treat hyperammonemia.
N,N-Dimethylurea (DMU) is a urea derivative and used as an intermediate in organic synthesis.
N,N-Dimethylurea (DMU) is a colorless crystalline powder with little toxicity.


N,N-Dimethylurea (DMU) is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.
In the textile processing industry N,N-Dimethylurea (DMU) is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.


N,N-Dimethylurea (DMU) is used pharmaceutical intermediates, also used in the production of fiber treatment agent.
N,N-Dimethylurea (DMU) is used in medicine to synthesize theophylline, caffeine and nificaran hydrochloride.
N,N-Dimethylurea (DMU) is used intermediate used in the production of Pharmaceuticals and Agrochemical.


Additionally, N,N-Dimethylurea (DMU) finds applications in agrochemicals, contributing to the synthesis of pesticides and herbicides.
The market benefits from the growth in these end-use industries, reflecting the compound’s versatility and importance in the production of high-value chemical products.


As pharmaceutical and agrochemical sectors continue to expand, the N,N-Dimethylurea (DMU) Market remains integral to supporting innovations and advancements within the broader chemical industry.”



PURIFICATION METHODS OF N,N-DIMETHYLUREA (DMU):
Crystallise the urea from acetone/diethyl ether by cooling in an ice bath.
Also crystallise N,N-Dimethylurea (DMU) from EtOH and dry it at 50o/5mm for 24hours.



REACTIVITY PROFILE OF N,N-DIMETHYLUREA (DMU):
N,N-Dimethylurea (DMU) is an amide.
Amides/imides react with azo and diazo compounds to generate toxic gases.
Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents.

Amides are very weak bases (weaker than water).
Imides are less basic yet and in fact react with strong bases to form salts.
That is, they can react as acids.

Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile.
The combustion of these compounds generates mixed oxides of nitrogen (NOx).



PHYSICAL and CHEMICAL PROPERTIES of N,N-DIMETHYLUREA (DMU):
Chemical formula: C3H8N2O
Molar mass: 88.110 g·mol−1
Appearance: Colorless, waxy crystals
Odor: Odorless
Density: 1.142 g mL−1
Melting point: 104.4 °C; 219.8 °F; 377.5 K
Boiling point: 269.1 °C; 516.3 °F; 542.2 K
Solubility in water: 765 g L−1
Magnetic susceptibility (χ): -55.1·10−6 cm3/mol
Thermochemistry:
Std enthalpy of formation (ΔfH⦵298): −312.1–−312.1 kJ mol−1
Std enthalpy of combustion (ΔcH⦵298): −2.0145–−2.0089 MJ mol−1
Molecular Weight: 88.11 g/mol

XLogP3: -0.5
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 0
Exact Mass: 88.063662883 g/mol
Monoisotopic Mass: 88.063662883 g/mol
Topological Polar Surface Area: 41.1Ų
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 46.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Physical state: flakes
Color: colorless
Odor: amine-like
Melting point/freezing point:
Melting point/range: 103 - 106 °C
Initial boiling point and boiling range: 268 - 270 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 157 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 9,0 - 9,5
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 765 g/l at 21,5 °C - soluble

Partition coefficient:
n-octanol/water: log Pow: -0,783
Vapor pressure: No data available
Density: 1,14 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: No data available
Other safety information:
Bulk density 0,50 g/l
Molecular Formula: CH3NHCONHCH3
CAS No: 96-31-1
EINECS: 202-498-7
Molecular Weight: 88.11
Appearance: White Crystals
Assay: ≥ 95%

Freezing point: 103'C Min
Volatile Content: ≤ 0.2%
Melting point: 104'C
CAS number: 96-31-1
EC number: 202-498-7
Hill Formula: C₃H₈N₂O
Chemical formula: CH₃NHCONHCH₃
Molar Mass: 88.11 g/mol
HS Code: 2924 19 00
Boiling point: 268 - 270 °C (1013 hPa)
Density: 1.14 g/cm3 (20 °C)
Flash point: 157 °C DIN 51758
Ignition temperature: 400 °C
Melting Point: 101 - 104 °C
pH value: 9.0 - 9.5 (H₂O)
Vapor pressure: Bulk density: 500 kg/m3
Solubility: 765 g/l

Chemical Name: N,N’-dimethylurea
CAS No.: 96-31-1
Molecular Formula: C3H8N2O
Molecular Weight: 88.10840
PSA: 41.13000
LogP: 0.32700
Appearance & Physical State: white flake
Density: 1.142
Boiling Point: 268-270ºC
Melting Point: 101-105ºC
Flash Point: 157ºC
Refractive Index: 1.413
Water Solubility: 765 g/L (21.5 ºC)
Stability: Stable under normal temperatures and pressures.
Storage Condition: Store at RT.
Melting point: 101-104 °C(lit.)
Boiling point: 268-270 °C(lit.)
Density: 1.142

vapor pressure: 6 hPa (115 °C)
refractive index: 1.4715 (estimate)
Flash point: 157 °C
storage temp.: Store below +30°C.
solubility: H2O: 0.1 g/mL, clear, colorless
pka: 14.57±0.46(Predicted)
form: Crystals
color: White
PH: 9.0-9.5 (100g/l, H2O, 20℃)
Water Solubility: 765 g/L (21.5 ºC)
BRN: 1740672
InChIKey: MGJKQDOBUOMPEZ-UHFFFAOYSA-N
LogP: -0.783 at 25℃
CAS DataBase Reference: 96-31-1(CAS DataBase Reference)
FDA UNII: WAM6DR9I4X
NIST Chemistry Reference: Urea, N,N'-dimethyl-(96-31-1)
EPA Substance Registry System: 1,3-Dimethylurea (96-31-1)

CAS No.: 96-31-1
Molecular Formula: C3H8N2O
InChIKeys: InChIKey=MGJKQDOBUOMPEZ-UHFFFAOYSA-N
Molecular Weight: 88.11
Exact Mass: 88.11
EC Number: 202-498-7
UNII: WAM6DR9I4X
ICSC Number: 1745
NSC Number: 24823|14910
DSSTox ID: DTXSID5025156
Color/Form: RHOMBIC BIPYRAMIDAL CRYSTALS FROM CHLOROFORM-ETHER|COLORLESS PRISMS
HScode: 2924199090
PSA: 41.1
XLogP3: -0.5
Appearance: N,n'-dimethylurea appears as colorless crystals. (NTP, 1992)
Density: 1.142 g/cm3

Melting Point: 108 °C
Boiling Point: 268-270 °C
Flash Point: 154°C
Refractive Index: 1.414
Water Solubility: H2O: 765 g/L (21.5 ºC)
Vapor Pressure: Vapour pressure, Pa at 20°C: 0.042
Air and Water Reactions: Water soluble.
Reactive Group: Amides and Imides
Autoignition Temperature: 400 °C
Molecular Formula / Molecular Weight: C3H8N2O = 88.11
Physical State (20 deg.C): Solid
CAS RN: 96-31-1
Reaxys Registry Number: 1740672
PubChem Substance ID: 87566985
SDBS (AIST Spectral DB): 2161
MDL Number: MFCD00008286
Appearance: colorless crystals (est)
Assay: 95.00 to 100.00

Food Chemicals Codex Listed: No
Melting Point: 108.00 °C. @ 760.00 mm Hg
Boiling Point: 269.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.547000 mmHg (est)
Flash Point: 116.00 °F. TCC ( 46.60 °C. ) (est)
logP (o/w): -0.490
Soluble in: water, 1.615e+004 mg/L @ 25 °C (est)
Synonyms: N,N'-Dimethylurea
Molecular Formula: C3H8N2O
Molecular Weight: 88.11
CAS Number: 96-31-1
EINECS: 202-498-7
Appearance: White powder
Density: 1.142
Melting Point: 101-105 ºC
Stability: Stable under ordinary conditions.
Appearance: White powder
PH value: 6.5-8.0

Assay: ≥97.5%
Water: ≤0.5
Density: 0.9±0.1 g/cm3
Boiling Point: 269.0±0.0 °C at 760 mmHg
Melting Point: 101-104 °C(lit.)
Molecular Formula: C3H8N2O
Molecular Weight: 88.108
Flash Point: 124.3±18.9 °C
Exact Mass: 88.063660
PSA: 41.13000
LogP: -1.01
Vapour Pressure: 0.0±0.5 mmHg at 25°C
Index of Refraction: 1.414
Storage condition: Store at RT.
Water Solubility: 765 g/L (21.5 ºC)
Synonyms: 1,3-dimethylurea
Molecular Weight: 88.11
Molecular Formula: C3H8N2O

Canonical SMILES: CNC(=O)NC
InChI: InChI=1S/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6)
InChIKey: MGJKQDOBUOMPEZ-UHFFFAOYSA-N
Boiling Point: 268-270 ℃
Melting Point: 101-105 ℃
Flash Point: 157ºC
Purity: > 98.0 % (GC)
Density: 1.142 g/cm3
Appearance: Colorless crystals.
Storage: Store at RT.
HS Code: 29241900
Log P: 0.32700
MDL: MFCD00008286
PSA: 41.13
Refractive Index: 1.413
Risk Statements: R62
RTECS: YS9868000
Safety Statements: S24/25
Stability: Stable under normal temperatures and pressures.



FIRST AID MEASURES of N,N-DIMETHYLUREA (DMU):
-Description of first-aid measures:
*General advice:
Consult a physician.
Show this material 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:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N-DIMETHYLUREA (DMU):
-Environmental precautions:
Do not let product 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.



FIRE FIGHTING MEASURES of N,N-DIMETHYLUREA (DMU):
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of N,N-DIMETHYLUREA (DMU):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
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:
Choose body protection
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N-DIMETHYLUREA (DMU):
-Precautions for safe handling:
*Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of N,N-DIMETHYLUREA (DMU):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

2,2'-{1,2-Propandiylbis[nitrilo(Z)methylyliden]}diphenol; 2,2'-{1,2-Propanediylbis[nitrilo(Z)methylylidene]}diphenol; 2,2'-{1,2-Propanediylbis[nitrilo(Z)méthylylidène]}diphénol; N,N'-bis(salicylidene)-1.2-propanediamine; N,N'-Disalicylidene-1,2-propanediamine; Phenol, 2,2'-[(1-methyl-1,2-ethanediyl)bis[nitrilo(Z)methylidyne]]bis- CAS NO:94-91-7

N-Ethyl-N-hydroxy-Ethanamine; N,N-Diethylhydroxylamine; DEHA CAS NO:3710-84-7

N-Ethyl-N-hydroxy-Ethanamine; N,N-Diethylhydroxylamine; DEHA CAS NO:3710-84-7

N,N'-Methylene-bis-acrylamide is the organic compound with the formula (H2C=CHCONH)2CH2.
N,N'-Methylene-bis-acrylamide is a raw material of photosensitive nylon or photosensitive plastic.
N,N'-Methylene-bis-acrylamide is a white crystalline powder with a neutral odor.



CAS Number: 110-26-9
EC Number: 203-750-9
MDL number: MFCD00008625
Linear Formula: (H2C=CHCONH)2CH2
Chemical formula: C7H10N2O2




Bis-acrylamide, N,N-Methylene-bis-acrylamide, N,N'-METHYLENEBISACRYLAMIDE, 110-26-9, N,N'-Methylenediacrylamide, N,N'-Methylene-bis-acrylamide, Methylenebisacrylamide, Bis-acrylamide, Methylenediacrylamide, n,n-methylenebisacrylamide, N,N'-Methylenebis(acrylamide), Bisacrylamide,
2-Propenamide, N,N'-methylenebis-, N-[(prop-2-enoylamino)methyl]prop-2-enamide, N,N'-Methylidenebisacrylamide, Acrylamide, N,N'-methylenebis-, N,N'-Methylenebis(2-propenamide), NSC 406836, MBAA, N-[(prop-2-enamido)methyl]prop-2-enamide, EDK4RIE19C, N,N'-methylene bisacrylamide, MLS001055454, DTXSID8025595, MFCD00008625, NSC-406836, Bisacrylamide, MBA, Methylenebisacrylamide NCGC00090721-03, SMR001227199, Acrylamide,N'-methylenebis-, N,N'-Methylenebis[acrylamide], 2-Propenamide,N'-methylenebis-, bis acrylamide, CCRIS 4672, EINECS 203-750-9, UNII-EDK4RIE19C, N-((PROP-2-ENOYLAMINO)METHYL)PROP-2-ENAMIDE, BRN 1706297, AI3-08643, NAPP, Methylenebis[acrylamide], cid_8041, n,n'-methylenebis acrylamide, n,n'-methylenebis-acrylamide, SCHEMBL20000, N-(acrylamidomethyl)acrylamide, N,N' methylene bis acrylamide, N,N`-Methylene-bis-acrylamide, DTXCID205595, N,N'-Diacryloylmethylenediamine, CHEMBL1401480, N,N'-Methylidenebis[acrylamide], BDBM74235, NSC7774, HY-D0848, N,N'-Methylenebis-Acrylamide, 2%, NSC-7774, Tox21_400038, NSC406836, AKOS005206740, AKOS025264600, N,N'-Methylenebis(acrylamide), 99%, N-[(Acryloylamino)methyl]acrylamide, METHYLENEBIS-ACRYLAMIDE, N,N'-, NCGC00090721-01, NCGC00090721-02, NCGC00090721-04, CAS-110-26-9, NCI60_041713, N,N'-METHYLENEBISACRYLAMIDE [INCI], N,N'-Methylenebisacrylamide, N,N'-Methylenebis(acrylamide), BB 0295285,
CS-0014818, CS-0202692, FT-0629399, M0506, M2877, E80374, EN300-104853, A905227, N-[(1-oxoprop-2-enylamino)methyl]-2-propenamide, Q3869308, W-108692, 26949-19-9, N,N'-Methylenebisacrylamide, bis-Acrylamide, Methylenebisacrylamide, N,N'-Methylenediacrylamide, BIS, MBA, BIS, METHYLENEBISACRYLAMIDE, N,N-METHYLENE-BIS-ACRYLAMIDE, BISACRYLAMIDE, napp, N,N-Methylenebisa, BIS MBA, N,N'-MethyL, enebisacryL, N,N'-MethyL, enebisacryL, N,N-Methylenebisa, Bis or Bis Acrylamide, N,N-Methylenebisacrylamide, N,N'-Methylenebisacrylamide, N,N'-Methylene bisacrylamide, N,N'-Diacryloylmethylenediamine, N,N'-Methylene-bis-(acrylamide), N,N'-Methylidenebis[acrylamide], N-[(Acryloylamino)methyl]acrylamide, N,N'-methylene-bis(acrylamide), N,N'-methylenebis-2-propenamide, Methylene bisacrylamide, N,N'-methylenebisacrylamide, N-{[(1-hydroxyprop-2-en-1-ylidene)amino]methyl}prop-2-enimidate, N,N'-METHYLENESBISACRYLAMIDE, N,N'-METHYLENEDIACRYLAMIDE, N,N'-METHYLENEBIS(ACRYLAMIDE)-HG, n,n'-methylenebis(2-propenamide), N, N-METHYLENE-BIS-ACRYLAMIDE, N,N'-METHYLENEBISACRYLAMIDE



N,N'-Methylene-bis-acrylamide is the organic compound with the formula (H2C=CHCONH)2CH2.
A colorless solid, N,N'-Methylene-bis-acrylamide is a crosslinking agent in polyacrylamides, e.g., as used for SDS-PAGE.
N,N'-Methylene-bis-acrylamide is a cross linking agent that polymerizes with acrylamide and creates cross links within the polyacrylamide gel.


N,N'-Methylene-bis-acrylamide is capable of creating a network rather than linear chains which helps in maintaining the firmness of gel.
N,N'-Methylene-bis-acrylamide is a cross-linker reagent used for precise, critical PAGE gels.
N,N'-Methylene-bis-acrylamide can react with acrylamide to produce breakdown fluid or react with monomer to produce insoluble resin.


N,N'-Methylene-bis-acrylamide is a white crystalline powder.
N,N'-Methylene-bis-acrylamide is white crystalline powder with a neutral odor.
N,N'-Methylene-bis-acrylamide is very slightly water soluble.


N,N'-Methylene-bis-acrylamide is soluble in water or methanol.
N,N'-Methylene-bis-acrylamide is soluble in water, ethanol and methanol.
N,N'-Methylene-bis-acrylamide is a white or light yellow powder crystals.


N,N'-Methylene-bis-acrylamide's melting point is 184 ℃ and (decomposition), relative density 1. 352 (30 ℃).
N,N'-Methylene-bis-acrylamide is soluble in water, but also soluble in ethanol, acetone and other organic solvents.
N,N'-Methylene-bis-acrylamide is a cross linking agent that readily polymerizes with acrylamide to create cross links within the polyacrylamide gel matrix.


N,N'-Methylene-bis-acrylamide effectively creates a network rather than linear chains, a property that helps in maintaining the firmness of gel.
N,N'-Methylene-bis-acrylamide belongs to the class of organic compounds known as acrylic acids and derivatives.
These are organic compounds containing acrylic acid CH2=CHCO2H or a derivative thereof.


Based on a literature review a significant number of articles have been published on N,N'-Methylene-bis-acrylamide.
N,N'-Methylene-bis-acrylamide has been identified in human blood as reported by (PMID: 31557052 ).
N,N'-Methylene-bis-acrylamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives.


N,N'-Methylene-bis-acrylamide is part of the human exposome.
N,N'-Methylene-bis-acrylamide is a cross linking agent that polymerizes with acrylamide and creates cross links within the polyacrylamide gel.
N,N'-Methylene-bis-acrylamide is capable of creating a network rather than linear chains which helps in maintaining the firmness of gel.


N,N'-Methylene-bis-acrylamide is a preparatory agent for polyacrylamide gels
The thickener for all water phase pigment printing is produced by copolymerization of N,N'-Methylene-bis-acrylamide with acrylamide and butyl acrylate, which is the key auxiliary for implementing the new process of all water phase pigment printing.


N,N'-Methylene-bis-acrylamide is a cross-linking agent used during the formation of polymers such as polyacrylamide.
N,N'-Methylene-bis-acrylamide's molecular formula is C7H10N2O2.
N,N'-Methylene-bis-acrylamide is a biochemical reagent that can be used as a biological material or organic compound for life science related research.


N,N'-Methylene-bis-acrylamide is white crystalline powder, soluble in water, soluble in ethanol, acetone and other organic solvents.
N,N'-Methylene-bis-acrylamide is a cross-linking agent used during the formation of polymers such as polyacrylamide.
N,N'-Methylene-bis-acrylamide's molecular formula is C7H10N2O2.


Bisacrylamide is used in biochemistry as N,N'-Methylene-bis-acrylamide is one of the compounds of the polyacrylamide gel (used for SDS-PAGE).
Bisacrylamide polymerizes with acrylamide and is capable of creating cross-links between polyacrylamide chains, thus creating a network of polyacrylamide rather than unconnected linear chains of polyacrylamide.


N,N'-Methylene-bis-acrylamide can be production of water-based fracturing fluid in the process of oilfield production process.
N,N'-Methylene-bis-acrylamide can be used in the pharmaceutical gel explosive, has a good stability and strong degree is big, good water resistance.
N,N'-Methylene-bis-acrylamide is the key to the implementation of total aqueous pigment printing process additives.


N,N'-Methylene-bis-acrylamide is available for high content of organic matter in water treatment decolorization, purification of the refined sugar and organic compounds, waste water treatment, to the heat source (removal rate 88%), the extraction of antibiotics streptomycin (300000 V/ml) adsorption styrene hydrochloride.


N,N'-Methylene-bis-acrylamide is used in water conservancy, power engineering, underground engineering, civil air defense engineering, tunnel engineering construction have stable foundation role, make the effect is very good, reliable quality of waterproof plugging grouting material.
N,N'-Methylene-bis-acrylamide is a cross linking agent that polymerizes with acrylamide and creates cross links within the polyacrylamide gel.
N,N'-Methylene-bis-acrylamide is capable of creating a network rather than linear chains which helps in maintaining the firmness of gel.



USES and APPLICATIONS of N,N'-METHYLENE-BIS-ACRYLAMIDE:
N,N'-Methylene-bis-acrylamide can be copolymerized with acrylamide to produce oilfield fracturing fluid, and copolymerized with a certain monomer to produce insoluble resin.
N,N'-Methylene-bis-acrylamide can be used as a water plugging grouting material or as a crosslinking agent.


N,N'-Methylene-bis-acrylamide is used in the production of printing and dyeing additives, napkins, health diapers, and other industrial absorbent resins.
N,N'-Methylene-bis-acrylamide is used Separation of biopolymer compounds (proteins, peptides, nucleic acids).
N,N'-Methylene-bis-acrylamide is used the crosslinking agent of polyacrylamide gel was prepared.


N,N'-Methylene-bis-acrylamide is used Polyacrylamide gel technology and clinical test.
N,N'-Methylene-bis-acrylamide is also widely used in electronics, papermaking, printing plate making, synthetic resin modification, coatings, adhesives, and other fields.


Cross-linking agent for preparation of polyacrylamide.
In underground buildings, the insoluble gel formed by AM and N,N'-Methylene-bis-acrylamide injected into the soil layer strengthens the soil layer to prevent water seepage.


Adding concrete can shorten the curing period of concrete and improve its water resistance.
N,N'-Methylene-bis-acrylamide is used organic intermediate, cross-linking agent.
N,N'-Methylene-bis-acrylamide also can be used as crosslink agent.


N,N'-Methylene-bis-acrylamide also can be used in auxiliary, table cloth, health care diaper and AQ.
N,N'-Methylene-bis-acrylamide is the material to separate the amino acid and the material of photosensitive nylon and plastic.
N,N'-Methylene-bis-acrylamide can be used as insoluble gel to reinforce the earth layer or added into the concrete to reduce the maintenance time and improve the resistance to water.


Moreover, N,N'-Methylene-bis-acrylamide also can be used in electronics, papermaking, printing, resin, coating and adhesive.
N,N'-Methylene-bis-acrylamide may be used in UV scanning gels.
N,N'-Methylene-bis-acrylamide should mixed with acrylamide for making polyacrylamide gels for use in protein and nucleic acid electrophoresis.


N,N'-Methylene-bis-acrylamide is an organic intermediate; cross-linking agent for preparation of polyacrylamides; in preparing poly-acrylamide gel for e1ectrophoresis, chemical grouting and other purposes; in NAPP and Nyloprint UV-cured printing plates.


N,N'-Methylene-bis-acrylamide is used as photosensitive nylon and photosensitive plastic raw materials, building grouting materials, also used in photography, printing, plate making, etc;
N,N'-Methylene-bis-acrylamide can be used as an efficient crosslinking agent in the polymerization of acrylic acid and acrylamide.


N,N'-Methylene-bis-acrylamide is an oil field fracturing fluid, super absorbent resin, water plugging agent, concrete additive, alcohol soluble photosensitive nylon resin, paper??
N,N'-Methylene-bis-acrylamide is an important additive in the synthesis of strong agent and water treatment flocculant.


N,N'-Methylene-bis-acrylamide and acrylamide copolymer can be made into oil field fracturing fluid, and a monomer copolymerization to prepare insoluble resin, can be used as water plugging grouting material.
N,N'-Methylene-bis-acrylamide can also be used as a cross-linking agent.


The application of photosensitive materials, water-absorbing materials, optical fiber cable coating and biotechnology is being developed abroad, but the application in this field in China needs to be further developed.
In addition, N,N'-Methylene-bis-acrylamide is also used in medical, cosmetics, paper processing, coatings, adhesives and other aspects.


N,N'-Methylene-bis-acrylamide is used as an intermediate and cross-linking agent utilized in the preparation of polymers like polyacrylamide.
N,N'-Methylene-bis-acrylamide is also used in biochemistry for the preparation of polyacrylamide gels, which is useful for the electrophoretic separation of nucleic acids and proteins.


Further, N,N'-Methylene-bis-acrylamide is employed in the synthesis of acrylic resin and adhesives.
In addition to this, N,N'-Methylene-bis-acrylamide is used as a plugging agent in oilfield drilling and construction grouting.
N,N'-Methylene-bis-acrylamide is used as an intermediate and cross-linking agent utilized in the preparation of polymers like polyacrylamide.


N,N'-Methylene-bis-acrylamide is also used in biochemistry for the preparation of polyacrylamide gels, which is useful for the electrophoretic separation of nucleic acids and proteins.
Further, N,N'-Methylene-bis-acrylamide is employed in the synthesis of acrylic resin and adhesives.


N,N'-Methylene-bis-acrylamide is used as an organic intermediate, cross-linking agent, for making polyacrylamides, and for preparing polyacrylamide gel for electrophoresis, chemical grouting, and other uses.
N,N'-Methylene-bis-acrylamide is used in the preparation of polyacrylamide gels for electrophoretic separation of nucleic acids and proteins.


N,N'-Methylene-bis-acrylamide has been used in gel preparation.
N,N'-Methylene-bis-acrylamide is used cross-linking agent for preparation of polyacrylamides.
N,N'-Methylene-bis-acrylamide can be used as water shutoff agent in oil field drilling operation and construction grouting operation, as well as crosslinking agent in the synthesis of acrylic resin and adhesives.


N,N'-Methylene-bis-acrylamide can be used as raw material of photosensitive nylon and photosensitive plastics, building grouting material, photography, printing, plate making, etc.
A cross-linking agent, N,N'-Methylene-bis-acrylamide is used in the formation of polymers, such as polyacrylamide.


N,N'-Methylene-bis-acrylamide therefore has an important role in gel electrophoresis (SDS-PAGE).
N,N'-Methylene-bis-acrylamide is used in the production of super absorbent resin.
Superabsorbent resin can be used to produce sanitary products with excellent water absorption.


N,N'-Methylene-bis-acrylamide can also be used in the production of agricultural water retaining agent.
N,N'-Methylene-bis-acrylamide is used in biochemistry as it is one of the compounds of the polyacrylamide gel.
A cross-linking agent, N,N'-Methylene-bis-acrylamide is used in the formation of polymers, such as polyacrylamide.
N,N'-Methylene-bis-acrylamide therefore has an important role in gel electrophoresis



SYNTHESIS OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
Acrylamide reacts with an aqueous solution of formaldehyde in the presence of copper(I) chloride as a polymerization inhibitor and sulfuric acid as catalyst to form N,N'-Methylene-bis-acrylamide with yields of 60 to 80%.
The reaction proceeds via N-hydroxymethylacrylamide, which can be detected in alkaline solution and decomposes in acid to give N,N'-Methylene-bis-acrylamide.

Using acrylamide and paraformaldehyde in 1,2-dichloroethane gives a clear solution upon heating, from which MBA crystallizes.
In aqueous media, acrylonitrile also reacts with formaldehyde to give crude N,N'-Methylene-bis-acrylamide, which can be purified by recrystallization with acetone/water.

As a symmetric, unconjugated divinyl monomer, N,N'-Methylene-bis-acrylamide can be used with suitable initiators in cyclopolymerizations to create linear, soluble polymers whose backbones are built from five- and seven-membered rings.
With acrylic and vinylic monomers such as acrylonitrile, acrylamide, and substituted acrylamides, N,N'-Methylene-bis-acrylamide can undergo radical copolymerization to form highly crosslinked gels, using peroxides, UV light, or redox initiators.

The properties of such gels are determined by the crosslink density, and targeted gel formation using N,N'-Methylene-bis-acrylamide crosslinking gives useful technical properties used in various applications, such as in adhesives, paints, and superabsorbent.
In biochemistry, N,N'-Methylene-bis-acrylamide is used for chromatography gels and polyacrylamide gel electrophoresis.



REACTIONS AND USES OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
Under basic conditions, N,N'-Methylene-bis-acrylamide reacts further with formaldehyde at the amide nitrogen to give N-hydroxymethyl,N,N′-methylenebisacrylamide.
Nucleophiles such as alcohols, amines, or thiols add across the activated vinyl groups, giving mixtures of mono- and disubstituted products.
As a bifunctional electron-poor dienophile, MBA reacts with electron-rich dienes, such as cyclopentadiene, in Diels–Alder reactions, giving the corresponding norbornene adducts.



REACTIVITY PROFILE OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
N,N'-Methylene-bis-acrylamide is incompatible with strong oxidizers, strong acids and strong bases.



ALTERNATIVE PARENTS OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
*Secondary carboxylic acid amides
*Organopnictogen compounds
*Organonitrogen compounds
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



PURIFICATION METHODS OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
Recrystallise the amide from MeOH (100g dissolved in 500mL boiling MeOH) and filter without suction in a warmed funnel.
Allow to stand at room temperature and then at -15oC overnight.
The crystals are collected with suction in a cooled funnel and washed with cold MeOH.
The crystals are air-dried in a warm oven.



SUBSTITUENTS OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
*Acrylic acid or derivatives
*Secondary carboxylic acid amide
*Carboxamide group
*Organic nitrogen compound
*Organic oxygen compound
*Organopnictogen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Organonitrogen compound
*Carbonyl group
*Aliphatic acyclic compound



PREPARATION METHOD OF N,N'-METHYLENE-BIS-ACRYLAMIDE:
Acrylonitrile method acrylonitrile and formaldehyde are hydrolyzed under the catalysis of sulfuric acid to generate methylene bisacrylamide sulfate, which is then neutralized by ammonia to precipitate methylene bisacrylamide crystals, and then washed and dried to obtain a finished product.
The acrylamide method produces N,N'-Methylene-bis-acrylamide by reacting acrylamide with formaldehyde in water or organic solvent under acidic catalysis, and then washing and drying to obtain a finished product.
N-methylol acrylamide method N,N'-Methylene-bis-acrylamide is produced from the reaction of N-methylol acrylamide and acrylamide under acidic conditions.



PHYSICAL and CHEMICAL PROPERTIES of N,N'-METHYLENE-BIS-ACRYLAMIDE:
Chemical formula: C7H10N2O2
Molar mass: 154.169 g·mol−1
Appearance: white solid
Melting point: 181–182 °C (358–360 °F; 454–455 K)
Physical state: powder
Color: white
Odor: characteristic odour
Melting point/freezing point:
Melting point/range: > 300 °C
Initial boiling point and boiling range: 333,8 °C at 1.013 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: Not applicable
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: 34,1 g/l at 20 °C
Partition coefficient: n-octanol/water:
log Pow: -0,08 at 25 °C
Bioaccumulation is not expected.
Vapor pressure: < 0,01 hPa
Density: 1,216 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:
Surface tension 70 mN/m at 1g/l at 20 °C
Molecular Weight: 154.17 g/mol
XLogP3-AA: 0.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 4

Exact Mass: 154.074227566 g/mol
Monoisotopic Mass: 154.074227566 g/mol
Topological Polar Surface Area: 58.2Ų
Heavy Atom Count: 11
Formal Charge: 0
Complexity: 167
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: 110-26-9
EC number: 203-750-9
Hill Formula: C₇H₁₀N₂O₂
Chemical formula: (CH₂CHCONH)₂CH₂
Molar Mass: 154.17 g/mol
HS Code: 2924 19 00

Density: 1.216 g/cm3 (20 °C)
Melting Point: 173.7 - 185.9 °C (decomposition)
pH value: >=5.0 (25 g/l, H₂O, 20 °C)
Vapor pressure: Bulk density: 200 kg/m3
form: powder
mp: >300 °C (lit.)
solubility water: soluble 20 g/L at 20 °C
storage temp.: 2-8°C
SMILES: string C=CC(=O)NCNC(=O)C=C
InChI: 1S/C7H10N2O2/c1-3-6(10)8-5-9-7(11)4-2/h3-4H,1-2,5H2,(H,8,10)(H,9,11)
InChI key: ZIUHHBKFKCYYJD-UHFFFAOYSA-N
CAS NUMBER: 110-26-9
MOLECULAR FORMULA: C7H10N2O2
MOLECULAR WEIGHT: 154.169 g/mol
BEILSTEIN REGISTRY NUMBER: 1706297
EC NUMBER: 203-750-9
MDL NUMBER: MFCD00008625

Melting point: >300 °C(lit.)
Boiling point: 277.52°C (rough estimate)
Density: 1.235
vapor density: 5.31 (vs air)
vapor pressure: 0-0.073Pa at 20-84.85℃
refractive index: 1.4880 (estimate)
storage temp.: 2-8°C
solubility: H2O: 20 mg/mL at 20 °C, clear, colorless
form: powder
pka: 13.07±0.46(Predicted)
color: White
PH: >=5.0 (25g/l, H2O, 20℃)
Odor: Odorless
PH Range: >5
Water Solubility: 0.01-0.1 g/100 mL at 18 ºC
Sensitive: Air & Light Sensitive
λmax: 528nm(H2O)(lit.)
BRN: 1706297
Stability: Light Sensitive

InChIKey: ZIUHHBKFKCYYJD-UHFFFAOYSA-N
LogP: -1.52--0.08 at 24-25℃ and pH4-10
Surface tension: 70.2-70.3mN/m at 1g/L and 20℃
Indirect Additives used in Food Contact Substances: N,N'-METHYLENEBIS(ACRYLAMIDE)
FDA 21 CFR: 175.105
CAS DataBase Reference: 110-26-9(CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: EDK4RIE19C
NIST Chemistry Reference: 2-Propenamide, n,n'-methylenebis-(110-26-9)
EPA Substance Registry System: N,N'-Methylenebisacrylamide (110-26-9)
CAS: 110-26-9
EINECS: 203-750-9
InChI: InChI=1/C7H10N2O2/c1-4(6(8)10)3-5(2)7(9)11/h1-3H2,(H2,8,10)(H2,9,11)
InChIKey: ZIUHHBKFKCYYJD-UHFFFAOYSA-N
Molecular Formula: C7H10N2O2
Molar Mass: 154.17
Density: 1.235
Melting Point: >300°C(lit.)
Boling Point: 277.52°C (rough estimate)
Flash Point: 245.1°C

Water Solubility: 0.01-0.1 g/100 mL at 18 ºC
Solubility: H2O: 20mg/mL at20°C, clear, colorless
Vapor Presure: 0-0.073Pa at 20-84.85℃
Vapor Density: 5.31 (vs air)
Appearance: White crystal
Color: White
Odor: Odorless
Maximum wavelength(λmax): ['528nm(H2O)(lit.)']
BRN: 1706297
pKa: 13.07±0.46(Predicted)
PH: >=5.0 (25g/l, H2O, 20℃)
Storage Condition: 2-8°C
Sensitive: Air & Light Sensitive
Refractive Index: 1.4880 (estimate)
MDL: MFCD00008625
Chemical Formula: C7H10N2O2
Average Molecular Weight: 154.169
Monoisotopic Molecular Weight: 154.07422757
IUPAC Name: N-{[(1-hydroxyprop-2-en-1-ylidene)amino]methyl}prop-2-enimidic acid

Traditional Name: N-{[(1-hydroxyprop-2-en-1-ylidene)amino]methyl}prop-2-enimidic acid
CAS Registry Number: Not Available
SMILES: OC(C=C)=NCN=C(O)C=C
InChI Identifier: InChI=1S/C7H10N2O2/c1-3-6(10)8-5-9-7(11)4-2/h3-4H,1-2,5H2,(H,8,10)(H,9,11)
InChI Key: ZIUHHBKFKCYYJD-UHFFFAOYSA-N
Density: 1.1±0.1 g/cm3
Boiling Point: 445.1±41.0 °C at 760 mmHg
Melting Point: >300 °C(lit.)
Molecular Formula: C7H10N2O2
Molecular Weight: 154.167
Flash Point: 215.0±27.8 °C
Exact Mass: 154.074234
PSA: 58.20000
LogP: -1.44
Vapour density: 5.31 (vs air)
Vapour Pressure: 0.0±1.1 mmHg at 25°C
Index of Refraction: 1.475
Storage condition: 2-8°C
Water Solubility: 0.01-0.1 g/100 mL at 18 ºC



FIRST AID MEASURES of N,N'-METHYLENE-BIS-ACRYLAMIDE:
-Description of first-aid measures:
*General advice:
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.
Consult a physician.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
Give water to drink (two glasses at most).
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N'-METHYLENE-BIS-ACRYLAMIDE:
-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 carefully.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of N,N'-METHYLENE-BIS-ACRYLAMIDE:
-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 N,N'-METHYLENE-BIS-ACRYLAMIDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P3
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N'-METHYLENE-BIS-ACRYLAMIDE:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.
*Storage stability:
Recommended storage temperature: 2 - 8 °C
Air and light sensitive.



STABILITY and REACTIVITY of N,N'-METHYLENE-BIS-ACRYLAMIDE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Incompatible materials:
no information available

N,N'-Methylenebismorpholine is colorless liquid, soluble in water.
N,N’-Methylenebismorpholine is a highly concentrated industrial bactericide based on tetrahydrooxazines.
N,N’-Methylenebismorpholine is effective against gram-negative and gram positive bacterias.


CAS Number: 5625-90-1
EC Number: 227-062-3
MDL Number: MFCD00023369
Molecular Formula: C9H18N2O2


N,N'-Methylenebismorpholine is a low toxicity broad spectrum fungicide for water-based metalworking fluid.
N,N'-Methylenebismorpholine is soluble in water.
N,N’-Methylenebismorpholine, also known as dimethylformamide (DMF), is an organic compound belonging to the class of amides, and is one of the most widely used solvents in the world.


N,N’-Methylenebismorpholine is soluble in water.
N,N'-Methylenebismorpholine is a colorless, volatile liquid with a characteristic odor and a relatively low boiling point.
Owing to its good solubility N,N’-Methylenebismorpholine is suitable for oily as well as aqueous systems.


N,N’-Methylenebismorpholine is a highly concentrated industrial bactericide based on tetrahydrooxazines.
N,N'-Methylenebismorpholine, also known as dimethylformamide (DMF), is an organic compound belonging to the class of amides, and is one of the most widely used solvents in the world.



USES and APPLICATIONS of N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is used for Water Based Cutting Fluid.
N,N’-Methylenebismorpholine is employed as intermediate for pharmaceutical.
Compared to hexahydrotriazines and oxazolidines, N,N’-Methylenebismorpholine is more stable in metalworking concentrates.


N,N'-Methylenebismorpholine is also used in the synthesis of pharmaceuticals and agrochemicals, and as a solvent for the extraction of natural products.
N,N'-Methylenebismorpholine is widely used as a low toxicity broad spectrum fungicide for water-based metalworking fluid.
In addition, N,N’-Methylenebismorpholine is used in the preparation of catalysts, in the synthesis of polymers, and in the preparation of functionalized materials.


N,N’-Methylenebismorpholine is widely used as a low toxicity broad spectrum fungicide for water-based metalworking fluid.
N,N'-Methylenebismorpholine is also used in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals.
With the benefits of low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal, this biocide N,N'-Methylenebismorpholine is well-known in the MWFs additives.


N,N’-Methylenebismorpholine is also used in the synthesis of pharmaceuticals and agrochemicals, and as a solvent for the extraction of natural products.
N,N’-Methylenebismorpholine is employed as intermediate for pharmaceutical.
N,N'-Methylenebismorpholine is an important industrial solvent and is used in a variety of industries, including pharmaceuticals, chemicals, plastics, and adhesives.


N,N’-Methylenebismorpholine is also used in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals.
With the benefits of low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal, this biocide N,N’-Methylenebismorpholine is well-known in the MWFs additives.


N,N'-Methylenebismorpholine is employed as intermediate for pharmaceutical.
N,N'-Methylenebismorpholine is employed as intermediate for pharmaceutical.
N,N’-Methylenebismorpholine should be used at an addition level of 2 – 6% in a concentrate and at 0.3% in finished cutting fluid user dilutions, in order to have a concentration of 1,000 to 1,500 ppm of the active.


N,N’-Methylenebismorpholine is an important industrial solvent and is used in a variety of industries, including pharmaceuticals, chemicals, plastics, and adhesives.
In addition, N,N'-Methylenebismorpholine is used in the preparation of catalysts, in the synthesis of polymers, and in the preparation of functionalized materials.
N,N’-Methylenebismorpholine is successfully applied for the preservation, mineral oil containing, water-miscible coolants.



SCIENTIFIC RESEARCH APPLICATION OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine has a wide range of applications in scientific research, including as a solvent for organic synthesis, as a reagent for the synthesis of organic compounds, and as a medium for chromatography.



ADVANTAGES AND LIMITATIONS FOR LAB EXPERIMENTS OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine has several advantages for laboratory experiments.
N,N'-Methylenebismorpholine is a relatively inexpensive solvent, and is widely available.
N,N'-Methylenebismorpholine is also a relatively non-toxic solvent, and can be used in a variety of reactions.



FEATURE OF N,N'-METHYLENEBISMORPHOLINE:
1. Anti-bacteria and fungl effectively.
2. MBM fully meet with the requirements of water-based metalworking fluid;
3. N,N'-Methylenebismorpholine has low skin irritation, mild odor, low toxicity;
4. Formulation compatibility, lasting bactericidal.
At higher concentrations, fungi and molds also have better inhibition.



BENEFITS OF N,N'-METHYLENEBISMORPHOLINE:
1, a low toxicity broad spectrum fungicide for water-based metalworking fluid
2, anti-Bacteria and fungi effectively
3, fully meet with the requirements of water-based metalworking fluid: low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal.
At higher concentrations, fungi and molds also have better inhibition.
Recommended addition amount (mass ratio): Recipe 2-3%, the working liquid 1-2‰;



FUTURE DIRECTIONS OF N,N'-METHYLENEBISMORPHOLINE:
There are a number of potential future directions for the use of N,N'-Methylenebismorpholine.
One potential direction is the development of new methods for the synthesis of organic compounds, as dimorphoN,N'-Methylenebismorpholine linomethane can facilitate the reaction of different molecules by allowing them to interact with each other more easily.
Another potential direction is the development of new catalysts and functionalized materials, as N,N'-Methylenebismorpholine can act as a proton acceptor and facilitate the formation of hydrogen bonds between molecules.
Finally, further research into the use of N,N'-Methylenebismorpholine as a solvent for the extraction of natural products could help to identify potential applications in the pharmaceutical and agrochemical industries.



SYNTHESIS METHOD OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is synthesized through a variety of methods, including the reaction of dimethyl sulfate with ammonium hydroxide, the reaction of formaldehyde with dimethyl sulfate, and the reaction of dimethyl sulfoxide with formaldehyde.
N,N'-Methylenebismorpholine can also be synthesized through the reaction of dimethyl sulfoxide with ammonia, and through the reaction of dimethyl sulfoxide with formic acid.



BIOCHEMICAL AND PHYSIOLOGICAL EFFECTS OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is a volatile, colorless liquid with a characteristic odor.



MECHANISM OF ACTION OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is a polar aprotic solvent, meaning that it has a low dielectric constant and a low boiling point.
This makes it an ideal solvent for many organic reactions, as N,N'-Methylenebismorpholine has a low solubility for most organic compounds.
As a result, N,N'-Methylenebismorpholine can facilitate the reaction of different molecules by allowing them to interact with each other more easily.
In addition, N,N'-Methylenebismorpholine can act as a proton acceptor, allowing the formation of hydrogen bonds between molecules.



PHYSICAL and CHEMICAL PROPERTIES of N,N'-METHYLENEBISMORPHOLINE:
Appearance: Colorless liquid
Density: 1.05-1.10g/cm3
PH (1% water): 9.0-11.5
Solubility in Water: completely
Molecular Formula: C9H18N2O2
Molar Mass: 186.25
Density: 1,04 g/cm3
Boling Point: 122-124°C 12mm
Flash Point: 77.6°C
Water Solubility: Soluble in water.
Vapor Presure: 0.00935mmHg at 25°C
pKa: 6.91±0.10(Predicted)
Storage Condition: 2-8°C
Refractive Index: 1.4790 (estimate)

Molecular Weight: 186.25
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 2
Exact Mass: 186.136827821
Monoisotopic Mass: 186.136827821
Topological Polar Surface Area: 24.9 Ų
Heavy Atom Count: 13
Formal Charge: 0
Complexity: 127
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 Formula: C9H18N2O2
Molar Mass: 186.25
Density: 1,04 g/cm3
Boling Point: 122-124°C 12mm
Flash Point: 77.6°C
Water Solubility: Soluble in water.
Vapor Presure: 0.00935mmHg at 25°C
pKa: 6.91±0.10(Predicted)
Storage Condition: 2-8°C
Refractive Index: 1.4790 (estimate)
Density: 1.1±0.1 g/cm3
Boiling Point: 265.1±35.0 °C at 760 mmHg
Molecular Formula: C9H18N2O2
Molecular Weight: 186.251
Flash Point: 77.6±23.2 °C
Exact Mass: 186.136826
PSA: 24.94000
LogP: -0.06
Vapour Pressur: 0.0±0.5 mmHg at 25°C
Index of Refraction: 1.497

Purity of Active Content: >92%
Appearance: Colorless liquid
Density: 1.08-1.10g/cm3
Boiling point °C: 122-124(P=12torr)
PH (1% water): 9.0-11.0
Solubility in Water: completely
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/freezing point:
Melting point/range: 18 - 21 °C
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: 115 °C - open cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 16 mPa.s at 20 °C proportions, Hydrolysis
Partition coefficient: n-octanol/water:
log Pow: < 0,3 at 30 °C
Vapor pressure: No data available
Density: No data available
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
Boiling point: 122-124°C 12mm
Density: 1,04 g/cm3
refractive index: 1.4790 (estimate)
storage temp.: 2-8°C
pka: 6.91±0.10(Predicted)
Water Solubility: Soluble in water.



FIRST AID MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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 carefully with liquid-absorbent material.
Dispose of properly.



FIRE FIGHTING MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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 N,N'-METHYLENEBISMORPHOLINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N'-METHYLENEBISMORPHOLINE:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.



STABILITY and REACTIVITY of N,N'-METHYLENEBISMORPHOLINE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SYNONYMS:
4,4'-Methylenene (MORPHOLINE)
4,4'-Methylenebismorpholine
Bis (Morpholino) Methane
Methylenebismorpholine
Morpholine, 4,4'-Methylenebis-
Morpholine, 4,4'-amthylenedi-
n, n'-methalenebismorpholine
N,N'-Dimorpholinomethane
4,4'-methylenedimorpholine
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
5625-90-1
Dimorpholinomethane
N,N'-Dimorpholinomethane
4,4'-Methylenedimorpholine
4,4-Methylenedimorpholine
4-(morpholin-4-ylmethyl)morpholine
N,N'-Methylenebismorpholine
Morpholine, 4,4'-methylenebis-
bis(4-morpholinyl)methane
n,n'-methylene-bis-morpholine
MORPHOLINE, 4,4'-METHYLENEDI-
MFCD00023369
4,4'-Methylenebismorpholine
7O79DZW79Z
4-[(morpholin-4-yl)methyl]morpholine
Bismorpholino methane
Dimorpholinomethone
Bis(morpholino-)methan
EINECS 227-062-3
BRN 0111886
UNII-7O79DZW79Z
AI3-62944
bismorpholinomethane
Contram ST-1
methylenebismorpholine
bis(morpholino)methane
N,N\'-Dimorpholinomethane
4,4-methylene-bismorpholine
Oprea1_332757
4,4'-methanediyldimorpholine
N,N'-Methylene bismorpholine
4-27-00-00203 (Beilstein Handbook Reference)
SCHEMBL536772
DTXSID8052859
Bis(4-morpholinyl)methane, 98%
ZINC19324145
AKOS002314380
4,4'-METHYLENEBIS(MORPHOLINE)
FS-4049
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-
AC-12628
SY032818
DB-052882
CS-0236719
FT-0629594
EN300-172423
Q865946
W-110051
F2163-0188
N,N'-DIMORPHOLINOMETHANE
4,4'-methylenedi-morpholin
4,4'-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N'-Methylenebismorpholine
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
N,N'-DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
Morpholine,4,4-methylenebis-
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4'-methanediyldimorpholine
-bis-morpholine
4,4′-Methylenebis[morpholine]
4,4′-Methylenedimorpholine
4,4'-Dimorpholinylmethane
4,4'-Methylenebismorpholine
44METHYLENEBISMORPHOLINE
BIS-(MORPHOLINE-)METHANE
Bis(morpholino)methane
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
Methylenebismorpholine
Methylene-bis-morpholine,N,N'-
Morpholine, 4,4′-methylenebis-
Morpholine, 4,4′-methylenedi-
Morpholine,4,4-Methylenebis-
MORPHOLINE44METHYLENEDI
N,N′-Methylenebismorpholine;
N,N′-methylenebismorpholine
formaldehyde released from N,N′-methylenebismorpholine
N,N′-methylenebismorpholine
formaldehyde released by N,N′-methylenebismorpholine / MBM
DIMORPHOLINOMETHANE
4,4’-methylenedi-morpholin
4,4’-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N’-Methylenebismorpholine
DIMORPHOLINOMETHANE
N,N'-DIMORPHOLINOMETHANE
4,4’-methylenedi-morpholin
4,4’-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N’-Methylenebismorpholine
DIMORPHOLINOMETHONE
Morpholine,4,4-Methylenebis-
Methylene-bis-morpholine,N,N'-
MORPHOLINE44METHYLENEDI
44METHYLENEBISMORPHOLINE
BIS-(MORPHOLINE-)METHANE
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-
DIMORPHOLINOMETHONE
N,N'-Dimorpholinomethane
N,N´-Methylene bismorpholine
Bis (morpholino-) methan
Bismorpholino methane
4,4-Methylenedimorpholine
Morpholine, 4,4-methylenedi-
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-
N,N-Dimorpholinomethane
Morpholine,4,4-methylenebis-
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4'-methanediyldimorpholine
4,4-methylenebis-Morpholine
N,N-Methylene-bis-morpholine

N,N'-Methylenebismorpholine, also known as dimethylformamide (DMF), is an organic compound belonging to the class of amides, and is one of the most widely used solvents in the world.
N,N'-Methylenebismorpholine is a colorless, volatile liquid with a characteristic odor and a relatively low boiling point.


CAS Number: 5625-90-1
EC Number: 227-062-3
MDL Number: MFCD00023369
Molecular Formula: C9H18N2O2


N,N'-Methylenebismorpholine is soluble in water.
N,N’-Methylenebismorpholine is a highly concentrated industrial bactericide based on tetrahydrooxazines.
Owing to its good solubility N,N’-Methylenebismorpholine is suitable for oily as well as aqueous systems.


N,N’-Methylenebismorpholine is soluble in water.
N,N’-Methylenebismorpholine is effective against gram-negative and gram positive bacterias.
N,N’-Methylenebismorpholine, also known as dimethylformamide (DMF), is an organic compound belonging to the class of amides, and is one of the most widely used solvents in the world.



USES and APPLICATIONS of N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is widely used as a low toxicity broad spectrum fungicide for water-based metalworking fluid.
With the benefits of low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal, this biocide N,N'-Methylenebismorpholine is well-known in the MWFs additives.
N,N'-Methylenebismorpholine is employed as intermediate for pharmaceutical.


N,N'-Methylenebismorpholine is an important industrial solvent and is used in a variety of industries, including pharmaceuticals, chemicals, plastics, and adhesives.
N,N'-Methylenebismorpholine is also used in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals.
N,N'-Methylenebismorpholine is also used in the synthesis of pharmaceuticals and agrochemicals, and as a solvent for the extraction of natural products.


In addition, N,N'-Methylenebismorpholine is used in the preparation of catalysts, in the synthesis of polymers, and in the preparation of functionalized materials.
N,N'-Methylenebismorpholine is employed as intermediate for pharmaceutical.
N,N’-Methylenebismorpholine is successfully applied for the preservation, mineral oil containing, water-miscible coolants.


Compared to hexahydrotriazines and oxazolidines, N,N’-Methylenebismorpholine is more stable in metalworking concentrates.
N,N’-Methylenebismorpholine should be used at an addition level of 2 – 6% in a concentrate and at 0.3% in finished cutting fluid user dilutions, in order to have a concentration of 1,000 to 1,500 ppm of the active.
N,N’-Methylenebismorpholine is widely used as a low toxicity broad spectrum fungicide for water-based metalworking fluid.


With the benefits of low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal, this biocide N,N’-Methylenebismorpholine is well-known in the MWFs additives.
N,N’-Methylenebismorpholine is employed as intermediate for pharmaceutical.
N,N’-Methylenebismorpholine is an important industrial solvent and is used in a variety of industries, including pharmaceuticals, chemicals, plastics, and adhesives.


N,N’-Methylenebismorpholine is also used in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals.
N,N’-Methylenebismorpholine is also used in the synthesis of pharmaceuticals and agrochemicals, and as a solvent for the extraction of natural products.


In addition, N,N’-Methylenebismorpholine is used in the preparation of catalysts, in the synthesis of polymers, and in the preparation of functionalized materials.
N,N’-Methylenebismorpholine is employed as intermediate for pharmaceutical.



BENEFITS OF N,N'-METHYLENEBISMORPHOLINE:
1, a low toxicity broad spectrum fungicide for water-based metalworking fluid
2, anti-Bacteria and fungi effectively
3, fully meet with the requirements of water-based metalworking fluid: low skin irritation, mild odor, low toxicity; formulation compatibility, lasting bactericidal.
At higher concentrations, fungi and molds also have better inhibition.
Recommended addition amount (mass ratio): Recipe 2-3%, the working liquid 1-2‰;



SYNTHESIS METHOD OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is synthesized through a variety of methods, including the reaction of dimethyl sulfate with ammonium hydroxide, the reaction of formaldehyde with dimethyl sulfate, and the reaction of dimethyl sulfoxide with formaldehyde.
N,N'-Methylenebismorpholine can also be synthesized through the reaction of dimethyl sulfoxide with ammonia, and through the reaction of dimethyl sulfoxide with formic acid.



SCIENTIFIC RESEARCH APPLICATION OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine has a wide range of applications in scientific research, including as a solvent for organic synthesis, as a reagent for the synthesis of organic compounds, and as a medium for chromatography.



MECHANISM OF ACTION OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is a polar aprotic solvent, meaning that it has a low dielectric constant and a low boiling point.
This makes it an ideal solvent for many organic reactions, as N,N'-Methylenebismorpholine has a low solubility for most organic compounds.
As a result, N,N'-Methylenebismorpholine can facilitate the reaction of different molecules by allowing them to interact with each other more easily.
In addition, N,N'-Methylenebismorpholine can act as a proton acceptor, allowing the formation of hydrogen bonds between molecules.



BIOCHEMICAL AND PHYSIOLOGICAL EFFECTS OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine is a volatile, colorless liquid with a characteristic odor.



ADVANTAGES AND LIMITATIONS FOR LAB EXPERIMENTS OF N,N'-METHYLENEBISMORPHOLINE:
N,N'-Methylenebismorpholine has several advantages for laboratory experiments.
N,N'-Methylenebismorpholine is a relatively inexpensive solvent, and is widely available.
N,N'-Methylenebismorpholine is also a relatively non-toxic solvent, and can be used in a variety of reactions.



FUTURE DIRECTIONS OF N,N'-METHYLENEBISMORPHOLINE:
There are a number of potential future directions for the use of N,N'-Methylenebismorpholine.
One potential direction is the development of new methods for the synthesis of organic compounds, as dimorphoN,N'-Methylenebismorpholine linomethane can facilitate the reaction of different molecules by allowing them to interact with each other more easily.
Another potential direction is the development of new catalysts and functionalized materials, as N,N'-Methylenebismorpholine can act as a proton acceptor and facilitate the formation of hydrogen bonds between molecules.
Finally, further research into the use of N,N'-Methylenebismorpholine as a solvent for the extraction of natural products could help to identify potential applications in the pharmaceutical and agrochemical industries.



PHYSICAL and CHEMICAL PROPERTIES of N,N'-METHYLENEBISMORPHOLINE:
Molecular Weight: 186.25
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 2
Exact Mass: 186.136827821
Monoisotopic Mass: 186.136827821
Topological Polar Surface Area: 24.9 Ų
Heavy Atom Count: 13
Formal Charge: 0
Complexity: 127
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 Formula: C9H18N2O2
Molar Mass: 186.25
Density: 1,04 g/cm3
Boling Point: 122-124°C 12mm
Flash Point: 77.6°C
Water Solubility: Soluble in water.
Vapor Presure: 0.00935mmHg at 25°C
pKa: 6.91±0.10(Predicted)
Storage Condition: 2-8°C
Refractive Index: 1.4790 (estimate)
Density: 1.1±0.1 g/cm3
Boiling Point: 265.1±35.0 °C at 760 mmHg
Molecular Formula: C9H18N2O2
Molecular Weight: 186.251
Flash Point: 77.6±23.2 °C
Exact Mass: 186.136826
PSA: 24.94000
LogP: -0.06
Vapour Pressur: 0.0±0.5 mmHg at 25°C
Index of Refraction: 1.497

Purity of Active Content: >92%
Appearance: Colorless liquid
Density: 1.08-1.10g/cm3
Boiling point °C: 122-124(P=12torr)
PH (1% water): 9.0-11.0
Solubility in Water: completely
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/freezing point:
Melting point/range: 18 - 21 °C
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: 115 °C - open cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 16 mPa.s at 20 °C proportions, Hydrolysis
Partition coefficient: n-octanol/water:
log Pow: < 0,3 at 30 °C
Vapor pressure: No data available
Density: No data available
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
Boiling point: 122-124°C 12mm
Density: 1,04 g/cm3
refractive index: 1.4790 (estimate)
storage temp.: 2-8°C
pka: 6.91±0.10(Predicted)
Water Solubility: Soluble in water.



FIRST AID MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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 carefully with liquid-absorbent material.
Dispose of properly.



FIRE FIGHTING MEASURES of N,N'-METHYLENEBISMORPHOLINE:
-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 N,N'-METHYLENEBISMORPHOLINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N'-METHYLENEBISMORPHOLINE:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.



STABILITY and REACTIVITY of N,N'-METHYLENEBISMORPHOLINE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SYNONYMS:
5625-90-1
Dimorpholinomethane
N,N'-Dimorpholinomethane
4,4'-Methylenedimorpholine
4,4-Methylenedimorpholine
4-(morpholin-4-ylmethyl)morpholine
N,N'-Methylenebismorpholine
Morpholine, 4,4'-methylenebis-
bis(4-morpholinyl)methane
n,n'-methylene-bis-morpholine
MORPHOLINE, 4,4'-METHYLENEDI-
MFCD00023369
4,4'-Methylenebismorpholine
7O79DZW79Z
4-[(morpholin-4-yl)methyl]morpholine
Bismorpholino methane
Dimorpholinomethone
Bis(morpholino-)methan
EINECS 227-062-3
BRN 0111886
UNII-7O79DZW79Z
AI3-62944
bismorpholinomethane
Contram ST-1
methylenebismorpholine
bis(morpholino)methane
N,N\'-Dimorpholinomethane
4,4-methylene-bismorpholine
Oprea1_332757
4,4'-methanediyldimorpholine
N,N'-Methylene bismorpholine
4-27-00-00203 (Beilstein Handbook Reference)
SCHEMBL536772
DTXSID8052859
Bis(4-morpholinyl)methane, 98%
ZINC19324145
AKOS002314380
4,4'-METHYLENEBIS(MORPHOLINE)
FS-4049
AC-12628
SY032818
DB-052882
CS-0236719
FT-0629594
EN300-172423
Q865946
W-110051
F2163-0188
N,N'-DIMORPHOLINOMETHANE
4,4'-methylenedi-morpholin
4,4'-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N'-Methylenebismorpholine
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
N,N'-DIMORPHOLINOMETHANE
4,4’-methylenedi-morpholin
4,4’-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N’-Methylenebismorpholine
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
N,N'-Dimorpholinomethane
N,N´-Methylene bismorpholine
Bis (morpholino-) methan
Bismorpholino methane
4,4-Methylenedimorpholine
Morpholine, 4,4-methylenedi-
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-
N,N-Dimorpholinomethane
Morpholine,4,4-methylenebis-
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4'-methanediyldimorpholine
4,4-methylenebis-Morpholine
N,N-Methylene-bis-morpholine
N,N-Dimorpholinomethane
Morpholine,4,4-methylenebis-
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4'-methanediyldimorpholine
-bis-morpholine
4,4′-Methylenebis[morpholine]
4,4′-Methylenedimorpholine
4,4'-Dimorpholinylmethane
4,4'-Methylenebismorpholine
44METHYLENEBISMORPHOLINE
BIS-(MORPHOLINE-)METHANE
Bis(morpholino)methane
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
Methylenebismorpholine
Methylene-bis-morpholine,N,N'-
Morpholine, 4,4′-methylenebis-
Morpholine, 4,4′-methylenedi-
Morpholine,4,4-Methylenebis-
MORPHOLINE44METHYLENEDI
N,N′-Methylenebismorpholine;
N,N′-methylenebismorpholine
formaldehyde released from N,N′-methylenebismorpholine
N,N′-methylenebismorpholine
formaldehyde released by N,N′-methylenebismorpholine / MBM
DIMORPHOLINOMETHANE
N,N'-DIMORPHOLINOMETHANE
4,4’-methylenedi-morpholin
4,4’-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N’-Methylenebismorpholine
DIMORPHOLINOMETHONE
Morpholine,4,4-Methylenebis-
Methylene-bis-morpholine,N,N'-
MORPHOLINE44METHYLENEDI
44METHYLENEBISMORPHOLINE
BIS-(MORPHOLINE-)METHANE
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-

N,N'-Methylene-bis-morpholine is soluble in water.
N,N'-Methylene-bis-morpholine is synthesized using a proprietary process that ensures high purity and consistency.


CAS Number: 5625-90-1
EC Number: 227-062-3
MDL Number: MFCD00023369
Molecular formula: C9H18N2O2


N,N'-Methylene-bis-morpholine is a low toxicity broad spectrum fungicide for water-based metalworking fluid.
N,N'-Methylene-bis-morpholine is anti-Bacteria and fungi effectively.
N,N'-Methylene-bis-morpholine is fully meet with the requirements of water-based metalworking fluid.


N,N'-Methylene-bis-morpholine is soluble in water.
One of the key benefits of N,N'-Methylene-bis-morpholine is its ability to act as a chelating agent, meaning it can bind to metal ions and prevent them from reacting with other chemicals.


This property makes N,N'-Methylene-bis-morpholine an ideal additive in the production of pharmaceuticals, where it can help to stabilize active ingredients and prevent degradation over time.
In addition, N,N'-Methylene-bis-morpholine is a versatile solvent that can dissolve a wide range of organic compounds.


This makes N,N'-Methylene-bis-morpholine useful in the production of polymers and resins, where it can help to dissolve and disperse additives and other chemicals.
N,N'-Methylene-bis-morpholine is also used in the production of adhesives, where it can help to improve the viscosity and adhesion of the final product.


In terms of market prospects, N,N'-Methylene-bis-morpholine is a promising chemical that is expected to see continued growth in the coming years.
As the demand for polymers, resins, and pharmaceuticals continues to increase, the need for solvents and stabilizers like N,N'-Methylene-bis-morpholine will also rise.


Furthermore, the use of N,N'-Methylene-bis-morpholine in the production of PVC and other plastics is expected to grow as the demand for sustainable and eco-friendly materials increases.
This is due to the fact that N,N'-Methylene-bis-morpholine is a non-toxic and biodegradable chemical that can be easily recycled or disposed of.
N,N'-Methylene-bis-morpholine is synthesized using a proprietary process that ensures high purity and consistency.



USES and APPLICATIONS of N,N'-METHYLENE-BIS-MORPHOLINE:
N,N'-Methylene-bis-morpholine is mainly used in the production of rubber vulcanization accelerators, and also used in the synthesis of surfactants, textile printing and dyeing auxiliaries, medicines and pesticides.
N,N'-Methylene-bis-morpholine is also used as a catalyst for the polymerization of cis-butadiene, a corrosion inhibitor, and an optical bleach.


N,N'-Methylene-bis-morpholine is employed as intermediate for pharmaceutical.
N,N'-Methylene-bis-morpholine is also a solvent for dyes, resins, waxes, early gums, casein, and so on.
The salts of morpholine are also widely used.


Morpholine hydrochloride is an intermediate of organic synthesis. Morpholine fatty acid salt can be used as a coating agent for the skin of fruits or melons and vegetables, and can appropriately inhibit the respiration of the base and preventthe evaporation of water and the shrinkage of epidermis.
N,N'-Methylene-bis-morpholine is suitable for emulsions, semi-synthetic and synthetic metalworking fluids.


In conclusion, N,N'-Methylene-bis-morpholine is a highly versatile and useful chemical that offers a wide range of benefits for various industries.
Its ability to act as a chelating agent, solvent, and stabilizer make N,N'-Methylene-bis-morpholine an ideal additive in the production of polymers, resins, and pharmaceuticals.


N,N'-Methylene-bis-morpholine is employed as intermediate for pharmaceutical.
N,N'-Methylene-bis-morpholine is used primarily as a solvent in the production of polymers, resins, and pharmaceuticals.
N,N'-Methylene-bis-morpholine is also used as a stabilizer in the production of PVC and other plastics.



FEATURES OF N,N'-METHYLENE-BIS-MORPHOLINE:
● Broad-spectrum biocide, can effectively inhibit and kill bacteria, fungi and yeasts.
● N,N'-Methylene-bis-morpholine has good compatibility with additives such as surfactants in the formula, and has no adverse effect on the stability of the metalworking fluids.
● N,N'-Methylene-bis-morpholine helps to improve the PH value of the metalworking fluids.
● N, N'-Methylene-bis-morpholine has better inhibitory effect on mold and fungus at higher concentration.
● N,N'-Methylene-bis-morpholine can be used alone or in combination with other biocides.



PHYSICAL and CHEMICAL PROPERTIES of N,N'-METHYLENE-BIS-MORPHOLINE:
CAS: 5625-90-1
EINECS: 227-062-3
InChI: InChI=1/C9H18N2O2/c1-5-12-6-2-10(1)9-11-3-7-13-8-4-11/h1-9H2
InChIKey: MIFZZKZNMWTHJK-UHFFFAOYSA-N
Molecular Formula: C9H18N2O2
Molar Mass: 186.25
Density: 1,04 g/cm3
Boling Point: 122-124°C 12mm
Flash Point: 77.6°C
Water Solubility: Soluble in water.
Vapor Presure: 0.00935mmHg at 25°C
pKa: 6.91±0.10(Predicted)
Storage Condition: 2-8°C
Refractive Index: 1.4790 (estimate)
Molecular weight: 186.25
EINECS: 227-062-3
SMILES: N1(CN2CCOCC2)CCOCC1
InChI: MIFZZKZNMWTHJK-UHFFFAOYSA-N
InChIKey: 1S/C9H18N2O2/c1-5-12-6-2-10(1)9-11-3-7-13-8-4-11/h1-9H2
Water solubility: Soluble in water.
Density: 1,04 g/cm3
Boiling Point: 122-124°C 12mm
Notes: N,N'-Methylene bismorpholine uses and applications include: Biocide

Class: Specialty Chemicals
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/freezing point:
Melting point/range: 18 - 21 °C
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: 115 °C - open cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 16 mPa.s at 20 °C
Water solubility at 10 - 30 °C - miscible in all proportions, Hydrolysis
Partition coefficient: n-octanol/water:
log Pow: < 0,3 at 30 °C
Vapor pressure: No data available
Density: No data available
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
Appearance: Transparent liquid
Assay: 92%min
Color: 2max
Refractive index: 70-80
PH(1% aq.solution): 9.5-11.5
Formula : C9H18N2O2
Molecular Weight : 186
CAS NO. : 5625-90-1
Assay (G.C.) : ≥92%
Density : 1.08-1.1
Boiling point : 265.1ºC
Flash point : 80ºC
Boiling point: 122-124°C 12mm
Density: 1,04 g/cm3
refractive index: 1.4790 (estimate)
storage temp.: 2-8°C
pka: 6.91±0.10(Predicted)
Water Solubility: Soluble in water.
InChIKey: MIFZZKZNMWTHJK-UHFFFAOYSA-N

CAS DataBase Reference: 5625-90-1(CAS DataBase Reference)
FDA UNII: 7O79DZW79Z
EPA Substance Registry System: Morpholine, 4,4'-methylenebis- (5625-90-1)
Molecular Weight： 186.251
Exact Mass： 186.25
EC Number： 227-062-3
UNII： 7O79DZW79Z
DSSTox ID： DTXSID8052859
PSA： 24.94000
XLogP3： -0.06
Density： 1.0494 g/cm3 @ Temp: 20 °C
Boiling Point： 139-140 °C
Flash Point： 77.6±23.2 °C
Refractive Index： 1.497
Water Solubility： Soluble in water.
Molecular Weight: 186.25 g/mol
XLogP3-AA: -0.3
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 2
Exact Mass: 186.136827821 g/mol
Monoisotopic Mass: 186.136827821 g/mol
Topological Polar Surface Area: 24.9Ų

Heavy Atom Count: 13
Formal Charge: 0
Complexity: 127
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: 186.25
EINECS: 227-062-3
SMILES: N1(CN2CCOCC2)CCOCC1
InChI: MIFZ ZKZNMWTHJK-UHFFFAOYSA-N
InChIKey: 1S/C9H18N2O2/c1-5-12-6-2-10(1)9-11-3-7-13-8-4-11/h1-9H2
Water solubility: Soluble in water.
Density: 1,04 g/cm3
Boiling Point: 122-124°C 12mm
CAS: 5625-90-1
EINECS: 227-062-3
InChI: InChI=1/C9H18N2O2/c1-5-12-6-2-10(1)9-11-3-7-13-8-4-11/h1-9H2
InChIKey: MIFZZKZNMWTHJK-UHFFFAOYSA-N
Molecular Formula: C9H18N2O2
Molar Mass: 186.25
Density: 1,04 g/cm3
Boling Point: 122-124°C 12mm
Flash Point: 77.6°C
Water Solubility: Soluble in water.
Vapor Presure: 0.00935mmHg at 25°C
pKa: 6.91±0.10(Predicted)
Storage Condition: 2-8°C
Refractive Index: 1.4790 (estimate)



FIRST AID MEASURES of N,N'-METHYLENE-BIS-MORPHOLINE:
-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.
Call a physician immediately.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Do not attempt to neutralise.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of N,N'-METHYLENE-BIS-MORPHOLINE:
-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 carefully with liquid-absorbent material.
Dispose of properly.
Clean up affected area.


FIRE FIGHTING MEASURES of N,N'-METHYLENE-BIS-MORPHOLINE:
-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 N,N'-METHYLENE-BIS-MORPHOLINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of N,N'-METHYLENE-BIS-MORPHOLINE:
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.



STABILITY and REACTIVITY of N,N'-METHYLENE-BIS-MORPHOLINE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SYNONYMS:
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-
N,N'-DIMORPHOLINOMETHANE
4,4'-methylenedi-morpholin
4,4'-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N'-Methylenebismorpholine
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
N,N'-DIMORPHOLINOMETHANE
4,4’-methylenedi-morpholin
4,4’-methylenedimorpholine
bis(morpholino-)methan
bismorpholinomethane
N,N’-Methylenebismorpholine
DIMORPHOLINOMETHANE
DIMORPHOLINOMETHONE
N,N'-Dimorpholinomethane
N,N´-Methylene bismorpholine
Bis (morpholino-) methan
Bismorpholino methane
4,4-Methylenedimorpholine
Morpholine, 4,4-methylenedi-
Morpholine, 4,4'-methylenebis-
N,N'methylenebismorpholine
[formaldehyde released from N,N'-methylenebismorpholine]
[MBM]
Bis-acrylamide
N,N-Methylene-bis-acrylamide
N,N'-Methylenebis(2-propenamide)
MBA; NAPP
Bis-acrylamide
N,N-Methylene-bis-acrylamide
N,N'-Methylenebis(2-propenamide)
MBA; NAPP
4-(Morpholin-4-ylMethyl)Morpholine
Conncide MW
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
bismorpholinomethane
bis(morpholino-)methan
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
N,N'-DIMORPHOLINOMETHANE
Morpholine,4,4′-methylenebis-
Morpholine,4,4′-methylenedi-
4,4′-Methylenebis[morpholine]
Dimorpholinomethane
Bis(morpholino)methane
4,4′-Methylenedimorpholine
Methylenebismorpholine
N,N′-Methylenebismorpholine
5625-90-1
Dimorpholinomethane
N,N'-Dimorpholinomethane
4,4'-Methylenedimorpholine
4-(morpholin-4-ylmethyl)morpholine
4,4-Methylenedimorpholine
Morpholine, 4,4'-methylenebis-
N,N'-Methylenebismorpholine
bis(4-morpholinyl)methane
MORPHOLINE, 4,4'-METHYLENEDI-
MFCD00023369
4-[(morpholin-4-yl)methyl]morpholine
4,4'-Methylenebismorpholine
7O79DZW79Z
Bismorpholino methane
Dimorpholinomethone
n,n'-methylene-bis-morpholine
Bis(morpholino-)methan
EINECS 227-062-3
BRN 0111886
4,4-methylenebis-Morpholine
UNII-7O79DZW79Z
AI3-62944
bismorpholinomethane
Contram ST-1
methylenebismorpholine
bis(morpholino)methane
4,4-methylene-bismorpholine
Oprea1_332757
4,4'-methanediyldimorpholine
4-27-00-00203 (Beilstein Handbook Reference)
SCHEMBL536772
DTXSID8052859
AKOS002314380
4,4'-METHYLENEBIS(MORPHOLINE)
FS-4049
AC-12628
SY032818
CS-0236719
FT-0629594
EN300-172423
Q865946
W-110051
F2163-0188
Morpholine, 4,4'-methylenedi- (6CI,7CI,8CI)
4,4'-Methylenebis[morpholine]
Bis(morpholino)methane
Dimorpholinomethane
Methylenebismorpholine
N,N'-Methylenebismorpholine
Morpholine, 4,4′-methylenebis-
Morpholine, 4,4′-methylenedi-
4,4′-Methylenebis[morpholine]
Dimorpholinomethane
Bis(morpholino)methane
4,4′-Methylenedimorpholine
Methylenebismorpholine
N,N′-Methylenebismorpholine
DIMORPHOLINOMETHONE
DIMORPHOLINOMETHANE
N,N-Dimorpholinomethane
MORPHOLINE44METHYLENEDI
BIS-(MORPHOLINE-)METHANE
44METHYLENEBISMORPHOLINE
Bis(4-morpholinyl)methane
N,N'-Methylenebismorpholine
4,4-methylenebis-Morpholine
N,N'-Methylenebismorpholine
Morpholine,4,4-Methylenebis-
4,4'-methanediyldimorpholine
Morpholine,4,4-methylenebis-
N,N'-Methylene-bis-morpholine
Methylene-bis-morpholine,N,N'-

2-(Dimethylamino)Ethanol; N,N-Dimethyl-N-ethanolamine; N,N-Dimethyl-2-aminoethanol; beta-Dimethylaminoethyl alcohol; beta-hydroxyethyldimethylamine; Ddimethylaminoethanol; Deanol; Dimethylethanolamine; Dimethylaminoaethanol (German); N,N-Dimethyl-2-Hydroxyethylamine; N,N-Dimethylaminoethanol; N,N-dimethyl-N-(2-hydroxyethyl)amine; cas no: 108-01-0

Tetrasodium (1-hydroxyethylidene)bisphosphonate; Tetra Sodium Salt of 1-Hydroxy Ethylidene-1,1-Diphosphonic Acid; ETIDRONIC ACID, TETRASODIUM SALT; 1-Hydroxyethane-1,1-diphosphonic acid , Tetrasodium salt; 1-Hydroxyethylidene-1,1-diphosphonic acid, Tetrasodium salt; Sodium HEDP; HEDPS; 1-hydroxyethylidenedi(phosphonic acid), Tetrasodium salt; (Hydroxyethylidene) diphosphonic acid, Tetrasodium salt; Tetra Sodium Salt of 1-Hydroxy Ethylidene-1,1-Diphosphonic Acid CAS NO:3794-83-0

Tetrasodium (1-hydroxyethylidene)bisphosphonate; Tetra Sodium Salt of 1-Hydroxy Ethylidene-1,1-Diphosphonic Acid; ETIDRONIC ACID, TETRASODIUM SALT; 1-Hydroxyethane-1,1-diphosphonic acid , Tetrasodium salt; 1-Hydroxyethylidene-1,1-diphosphonic acid, Tetrasodium salt; Sodium HEDP; HEDPS; 1-hydroxyethylidenedi(phosphonic acid), Tetrasodium salt; (Hydroxyethylidene) diphosphonic acid, Tetrasodium salt; Tetra Sodium Salt of 1-Hydroxy Ethylidene-1,1-Diphosphonic Acid CAS NO:3794-83-0

Sodium bromide, commonly known as NaBr, is an ionic compound with the chemical formula NaBr.
NaBr (Sodium bromide) is a white crystalline powder that is highly soluble in water and has a salty taste.
NaBr (Sodium bromide) is an alkali metal halide and is composed of a sodium cation (Na+) and a bromide anion (Br−).

NaBr (Sodium bromide)
CAS Number: 7647-15-6
EC Number: 231-599-9



APPLICATIONS


NaBr (Sodium bromide) is used in the oil and gas industry as a completion and workover fluid.
NaBr (Sodium bromide) is used as a sedative for horses and other large animals.
NaBr (Sodium bromide) is used in the manufacture of photographic film and paper.

NaBr (Sodium bromide) is used as a flame retardant in some plastics.
NaBr (Sodium bromide) is used in some pharmaceuticals as a sedative and hypnotic agent.

NaBr (Sodium bromide) is used as a disinfectant in water treatment.
NaBr (Sodium bromide) is used in the production of other bromine compounds.

NaBr (Sodium bromide) is used in the preparation of certain dyes.
NaBr (Sodium bromide) is used in some veterinary medicines.
NaBr (Sodium bromide) is used in the manufacture of some specialty chemicals.

NaBr (Sodium bromide) is used in some hair and skincare products.
NaBr (Sodium bromide) is used as an electrolyte in some batteries.

NaBr (Sodium bromide) is used in the production of some agricultural chemicals.
NaBr (Sodium bromide) is used in the preparation of some perfumes and fragrances.

NaBr (Sodium bromide) is used in some dental procedures as an antiseptic and analgesic.
NaBr (Sodium bromide) is used in some food products as a preservative.
NaBr (Sodium bromide) is used in the synthesis of some organic compounds.

NaBr (Sodium bromide) is used in some swimming pools as a disinfectant and algae control agent.
NaBr (Sodium bromide) is used in the textile industry as a dyeing and printing auxiliary.

NaBr (Sodium bromide) is used in the preparation of some cosmetics.
NaBr (Sodium bromide) is used in the manufacture of some flame retardants.

NaBr (Sodium bromide) is used in some pulp and paper manufacturing processes.
NaBr (Sodium bromide) is used in the production of some biocides.

NaBr (Sodium bromide) is used in some metal finishing and plating processes.
NaBr (Sodium bromide) is used in some antifreeze and deicing products.


Sodium bromide (NaBr) has various applications in different fields, including:

Photography:

NaBr (Sodium bromide) is used as a source of bromide ions in silver bromide emulsion, which is used in photographic film and paper.


Oil drilling:

NaBr (Sodium bromide) is used as a completion and workover fluid in oil and gas drilling operations.
NaBr (Sodium bromide) is used to prevent the swelling of shale and clay formations and improve the stability of the wellbore.


Chemical synthesis:

NaBr (Sodium bromide) is used as a reagent in various chemical reactions, such as the preparation of organobromine compounds.


Water treatment:

NaBr (Sodium bromide) is used as a disinfectant in water treatment plants to control the growth of microorganisms.


Pharmaceutical industry:

NaBr (Sodium bromide) is used as an anticonvulsant in the treatment of epilepsy.


Animal health:

NaBr (Sodium bromide) is used in veterinary medicine as a sedative, anticonvulsant, and antiseptic.


Food industry:

NaBr (Sodium bromide) is used as a preservative in some food products, such as bread.


Flame retardants:

NaBr (Sodium bromide) is used as a flame retardant in some plastics, textiles, and other materials.


Textile industry:

NaBr (Sodium bromide) is used in the dyeing of textiles as a leveling agent to ensure even dyeing.


Chemical analysis:

NaBr (Sodium bromide) is used in the laboratory for the preparation of solutions and for the analysis of various chemical compounds.


Electroplating:

NaBr (Sodium bromide) is used in electroplating baths to deposit metallic coatings on substrates.


Heat transfer fluids:

NaBr (Sodium bromide) is used in heat transfer fluids to prevent corrosion and scale formation.


Metal processing:

NaBr (Sodium bromide) is used in metal processing to remove impurities from the surface of metals.


Glass industry:

NaBr (Sodium bromide) is used as a fluxing agent in the production of glass to lower the melting point of the materials.


Wood preservatives:

NaBr (Sodium bromide) is used as a wood preservative to protect the wood from decay and insect infestation.


Corrosion inhibitors:

NaBr (Sodium bromide) is used as a corrosion inhibitor in various industries to protect metals from corrosion.


Soil stabilization:

NaBr (Sodium bromide) is used in soil stabilization to improve the stability of soil and prevent erosion.


Bleaching agents:

NaBr (Sodium bromide) is used as a bleaching agent in the pulp and paper industry.


Swimming pool disinfection:

NaBr (Sodium bromide) is used in swimming pool disinfection to control the growth of algae and bacteria.


Polymer production:

NaBr (Sodium bromide) is used in the production of some polymers as a chain transfer agent.


Herbicides:

NaBr (Sodium bromide) is used in the formulation of some herbicides to control the growth of weeds.


Textile finishing:

NaBr (Sodium bromide) is used in textile finishing to improve the hand of the fabric.


Tanning industry:

NaBr (Sodium bromide) is used in the tanning industry as a deliming agent to remove lime from the hides.


Gas scrubbing:

NaBr (Sodium bromide) is used in gas scrubbing operations to remove impurities from the gas stream.


Fumigants:

NaBr (Sodium bromide) is used as a fumigant to control pests in some agricultural products.


NaBr (Sodium bromide) is used as a sedative in veterinary medicine.
NaBr (Sodium bromide) is used in the preparation of photographic emulsions.

NaBr (Sodium bromide) is used in the manufacturing of drilling fluids for oil and gas wells.
NaBr (Sodium bromide) is used as a reagent in the chemical industry.
NaBr (Sodium bromide) is used in the textile industry for dyeing and printing fabrics.

NaBr (Sodium bromide) is used as a flame retardant in plastics and textiles.
NaBr (Sodium bromide) is used in the production of brominated compounds, such as bromoalkanes and bromoesters.

NaBr (Sodium bromide) is used in the preparation of pharmaceuticals, such as sedatives and anticonvulsants.
NaBr (Sodium bromide) is used in the production of photographic chemicals, such as silver bromide.
NaBr (Sodium bromide) is used as a preservative in the food industry.

NaBr (Sodium bromide) is used in the production of bromine for disinfectants and pesticides.
NaBr (Sodium bromide) is used as a source of bromine for organic synthesis.

NaBr (Sodium bromide) is used in water treatment as a disinfectant and oxidizing agent.
NaBr (Sodium bromide) is used in the production of flame retardant materials for aircraft and other transportation vehicles.

NaBr (Sodium bromide) is used in the manufacture of synthetic fibers and polymers.
NaBr (Sodium bromide) is used as a laboratory reagent for various chemical reactions.

NaBr (Sodium bromide) is used in the production of pigments and dyes.
NaBr (Sodium bromide) is used in the production of ceramics and glass.
NaBr (Sodium bromide) is used as an electrolyte in some batteries.

NaBr (Sodium bromide) is used in the production of brominated flame retardants for electrical and electronic equipment.
NaBr (Sodium bromide) is used in the manufacture of photographic film and paper.

NaBr (Sodium bromide) is used in the production of silver bromide for photographic applications.
NaBr (Sodium bromide) is used in the production of surfactants and detergents.

NaBr (Sodium bromide) is used in the production of fire extinguishers.
NaBr (Sodium bromide) is used in the production of veterinary medicines and supplements for livestock.



DESCRIPTION


Sodium bromide, commonly known as NaBr, is an ionic compound with the chemical formula NaBr.
NaBr (Sodium bromide) is a white crystalline powder that is highly soluble in water and has a salty taste.
NaBr (Sodium bromide) is an alkali metal halide and is composed of a sodium cation (Na+) and a bromide anion (Br−).

NaBr (Sodium bromide) is a white crystalline powder.
NaBr (Sodium bromide) is an ionic compound with the chemical formula NaBr.
NaBr (Sodium bromide) has a high melting point of 747°C and a boiling point of 1,390°C.

NaBr (Sodium bromide) is soluble in water, but insoluble in most organic solvents.
NaBr (Sodium bromide) is hygroscopic, which means it readily absorbs moisture from the air.

NaBr (Sodium bromide) has a salty taste and is used as a food preservative.
NaBr (Sodium bromide) is an inorganic compound commonly used in the manufacture of photography, medicines, and drilling fluids.

NaBr (Sodium bromide) is a strong oxidizing agent and can react violently with reducing agents.
NaBr (Sodium bromide) is a halide salt and can form toxic fumes of bromine gas upon contact with acids, acid fumes, and oxidizing agents.
NaBr (Sodium bromide) is commonly used as a source of bromide ions in organic synthesis and as a reagent in analytical chemistry.

NaBr (Sodium bromide) is also used in the production of flame retardants, dyes, and disinfectants.
NaBr (Sodium bromide) can be used as a sedative in medicine and as a component of mineral supplements.

NaBr (Sodium bromide) can be used as a catalyst in some chemical reactions.
NaBr (Sodium bromide) is used in the oil and gas industry as a completion fluid to increase the density of drilling fluids.

NaBr (Sodium bromide) has a refractive index of 1.641, making it useful in the production of optical lenses and glass.
NaBr (Sodium bromide) can be used as a disinfectant for swimming pools and spas.
NaBr (Sodium bromide) is a non-combustible solid, but can enhance combustion of other substances.

NaBr (Sodium bromide) has a molar mass of 102.89 g/mol and a density of 3.203 g/cm³.
NaBr (Sodium bromide) can be toxic if ingested in large quantities and can cause skin and eye irritation upon contact.

NaBr (Sodium bromide) is stable under normal conditions, but can decompose at high temperatures or when exposed to strong oxidizing agents.
NaBr (Sodium bromide) has a wide range of applications in the food, pharmaceutical, and chemical industries.

NaBr (Sodium bromide) can be used as a coagulant in wastewater treatment and as a flux in metallurgy.
NaBr (Sodium bromide) is commonly used as a bromide source in the preparation of organobromine compounds.

NaBr (Sodium bromide) can react with chlorine to form sodium hypobromite, a disinfectant used in water treatment.
NaBr (Sodium bromide) is a common laboratory reagent and is readily available in most chemical supply stores.



PROPERTIES


Chemical formula: NaBr
Molar mass: 102.894 g/mol
Appearance: white crystalline powder
Odor: odorless
Density: 3.203 g/cm3
Melting point: 747 °C (1,377 °F; 1,020 K)
Boiling point: 1,390 °C (2,530 °F; 1,660 K)
Solubility in water: 90.5 g/100 mL (25 °C); 121 g/100 mL (50 °C)
Solubility in ethanol: 1.1 g/100 mL (20 °C)
Solubility in acetone: 0.37 g/100 mL (20 °C)
Solubility in methanol: 0.82 g/100 mL (20 °C)
Solubility in ammonia: 47.8 g/100 mL (20 °C)
Solubility in pyridine: 19.4 g/100 mL (20 °C)
Crystal structure: face-centered cubic (fcc)
Refractive index (nD): 1.641
Dielectric constant: 5.8
Thermal conductivity: 0.321 W/(cm·K)
Specific heat capacity: 0.825 J/(g·K)
Viscosity: 2.82 cP (25 °C)
pH of a 0.1 M aqueous solution: 7.5
Hazard identification number: UN 1564
NFPA 704 (fire diamond) rating: 0 1 0



FIRST AID


The first aid measures for sodium bromide (NaBr) depend on the type and severity of exposure.
Here are some general guidelines:

If NaBr (Sodium bromide) comes into contact with your skin or eyes, flush the affected area with plenty of water for at least 15 minutes.

If you inhale NaBr (Sodium bromide) dust or mist, move to an area with fresh air immediately and seek medical attention if you experience any breathing difficulties.

If you swallow NaBr (Sodium bromide), do not induce vomiting.
Rinse your mouth with water and drink plenty of water or milk to dilute the chemical.
Seek medical attention immediately.

If NaBr (Sodium bromide) comes into contact with clothing or other materials, remove the contaminated items and wash the affected skin thoroughly.


In case of any exposure to NaBr (Sodium bromide), it is important to seek medical attention promptly.



HANDLING AND STORAGE


Handling:

Wear appropriate personal protective equipment (PPE), such as gloves and eye/face protection, when handling NaBr.
Avoid contact with skin, eyes, and clothing.

Use in a well-ventilated area to avoid inhalation of dust or fumes.
Do not eat, drink or smoke when handling NaBr.
Do not mix with incompatible substances.


Storage:

Store NaBr in a cool, dry, well-ventilated area away from heat, sparks, and flame.
Keep container tightly closed when not in use.

Store away from incompatible materials.
Do not store near acids or acidic materials.

Store in a secure, upright position to prevent containers from falling or being knocked over.
Do not store in direct sunlight or in areas with high temperatures or humidity.



SYNONYMS


Sodium bromide anhydrous
Bromide salt of sodium
UNII-0JG1KSW2VL
Natriumbromid (German)
Bromure de sodium (French)
Sodio bromuro (Italian)
Bromuro de sodio (Spanish)
Halite
Sedoneural
Sedonevril
Sodium bromatum (Latin)
Sodium bromidum (Latin)
Sodiumbromide
Bromnatrium
UN1459
HSDB 940
EINECS 231-599-9
BRN 3587175
AI3-50287
DTXSID5023476
CTK1D9626
MolPort-003-926-011
ACT05680
CHEBI:63093
Bromide of sodium
Natrium bromatum
Sedoneural
Sodium bromatum
Bromnatrium
Sedoneural forte
Sodium bromide (NaBr)
Unii-767ip0y0sy
Bromide sodium
Sodium bromide, anhydrous
Bromide, sodium
Hydrobromic acid sodium salt
Natrium bromidum
Sedoneural N
Sodium bromide, puriss p.a., ACS reagent, ≥99.0%
UNII-767IP0Y0SY
7647-15-6
AI3-01964
Bromide of soda
LS-142227
Sodium bromide (anhydrous)
Sodium monobromide
Bromnatrii
DTXSID1022389
Natrii bromidum.

Na-CMC (Sodium carboxymethyl cellulose) is a white or slightly yellowish, almost odourless and tasteless hydroscopic powder, consisting of very fine particles, fine granules or fine fibres.
Na-CMC (Sodium carboxymethyl cellulose) is a water soluble polymer which can be used as a polyelectrolyte cellulose derivative.
Na-CMC (Sodium carboxymethyl cellulose) belongs to the class of anionic linear structured cellulose.

CAS Number: 9004-32-4
Molecular Formula: C6H7O2(OH)2CH2COONa
EINECS Number: 618-378-6

Na-CMC (Sodium carboxymethyl cellulose) is biodegradable, but not readily biodegradable, and it is not expected to bioaccumulate.
Na-CMC (Sodium carboxymethyl cellulose) is components consist of polysaccharide composed of fibrous tissues of plants.
Na-CMC (Sodium carboxymethyl cellulose) is a water dispersible sodium salt of carboxy-methyl ether of cellulose that forms a clear colloidal solution.

Na-CMC (Sodium carboxymethyl cellulose) is a hygroscopic material that has the ability to absorb more than 50% of water at high humidity.
Na-CMC (Sodium carboxymethyl cellulose) is also a natural polymeric derivative that can be used in detergents, food and textile industries.
Na-CMC (Sodium carboxymethyl cellulose) is a water-soluble polymer.

As a solution in water, Na-CMC (Sodium carboxymethyl cellulose) has thixotropic properties.
Na-CMC (Sodium carboxymethyl cellulose) is useful in helping to hold the components of pyrotechnic compositions in aqucous suspension (e.g., in the making of black match).
Na-CMC (Sodium carboxymethyl cellulose) is also an especially effective binder that can be used in small amounts in compositions, where the binder can intcrfere with the intended effect (e.g., in strobe compositions).

However, its sodium content obviously precludes its use in most color compositions.
Na-CMC (Sodium carboxymethyl cellulose) is manufactured from cellulose by various proccsses that replacc some of the hy drogen atoms in the hydroxyl[OH] groups of the cellulose molecule with acidic carboxymethyl [-CH2CO.OH] groups，which are neutralized to form the corresponding sodium salt.
Na-CMC (Sodium carboxymethyl cellulose) is white when pure; industrial grade material may be grayish-white or cream granules or powder.

Na-CMC (Sodium carboxymethyl cellulose) is a low concern for toxicity to aquatic organisms.
Na-CMC (Sodium carboxymethyl cellulose) is used for its thickening and swelling properties in a wide range of complex formulated products for pharmaceutical, food, home, and personal care applications, as well as in paper, water treatment, and mineral processing industries.
Na-CMC (Sodium carboxymethyl cellulose) is tackifier, at room temperature, it is non-toxic tasteless white flocculent powder, it is stable and soluble in water, aqueous solution is neutral or alkaline transparent viscous liquid, it is soluble in other water-soluble gums and resins, it is insoluble in organic solvents such as ethanol.

Na-CMC (Sodium carboxymethyl cellulose) is the substituted product of cellulosic carboxymethyl group.
According to their molecular weight or degree of substitution, Na-CMC (Sodium carboxymethyl cellulose) can be completely dissolved or insoluble polymer, the latter can be used as the weak acid cation of exchanger to separate neutral or basic proteins.
Na-CMC (Sodium carboxymethyl cellulose) can form highly viscous colloidal solution with adhesive, thickening, flowing, emulsifying, shaping, water, protective colloid, film forming, acid, salt, suspensions and other characteristics, and it is physiologically harmless, so it is widely used in the food, pharmaceutical, cosmetic, oil, paper, textiles, construction and other areas of production.

Na-CMC (Sodium carboxymethyl cellulose) is a white or slightly yellowish powder.
Na-CMC (Sodium carboxymethyl cellulose) or cellulose gum is a cellulose derivative with carboxymethyl groups (-CH2-COOH) bound to some of the hydroxyl groups of the glucopyranose monomers that make up the cellulose backbone.
Na-CMC (Sodium carboxymethyl cellulose) is often used as its sodium salt, sodium carboxymethyl cellulose.

Na-CMC (Sodium carboxymethyl cellulose) used to be marketed under the name Tylose, a registered trademark of SE Tylose.
A semisynthetic, water-soluble polymer in which CH 2 COOH groups are substituted on the glucose units of the cellulose chain through an ether link- age.
Since the reaction occurs in an alkaline medium, the prod- uct is the sodium salt of the carboxylic acid R-O- CH 2 COONa.

Na-CMC (Sodium carboxymethyl cellulose) for oenological use is prepared exclusively from wood by treatment with alkali and monochloroacetic acid or its sodium salt.
Na-CMC (Sodium carboxymethyl cellulose) inhibits tartaric precipitation through a "protective colloid" effect.
Na-CMC (Sodium carboxymethyl cellulose) a colorless, odorless, water-soluble polymer.

Sodium carboxymethyl cellulose, NaCMC or CMC, was first developed in 1947.
Commonly known as carboxymethyl cellulose, it is composed of the sodium salt of an alkaline modified cellulose.
Na-CMC (Sodium carboxymethyl cellulose) is water-soluble but will react with heavy metal salts to form films that are clear, tough and insoluble in water.

Na-CMC (Sodium carboxymethyl cellulose) is thixotropic, becoming less viscous when agitated.
In most cases, Na-CMC (Sodium carboxymethyl cellulose) functions as a polyelectrolyte.
Na-CMC (Sodium carboxymethyl cellulose) is used commercially in detergents, food product and as size for textiles and paper.

In conservation, Na-CMC (Sodium carboxymethyl cellulose) has been used as an adhesive for textiles and paper.
Aging studies indicate that most Na-CMC (Sodium carboxymethyl cellulose) polymers have very good stability with negligible discoloration or weight loss.
Na-CMC (Sodium carboxymethyl cellulose) is the sodium salt of carboxymethyl cellulose, an anionic derivative.

Na-CMC (Sodium carboxymethyl cellulose) is widely used in oral and topical pharmaceutical formulations, primarily for its viscosity-increasing properties.
Viscous aqueous solutions are used to suspend powders intended for either topical application or oral and parenteral administration.
Na-CMC (Sodium carboxymethyl cellulose) may also be used as a tablet binder and disintegrant, and to stabilize emulsions.

Higher concentrations, usually 3–6%, of the medium-viscosity grade are used to produce gels that can be used as the base for applications and pastes; glycols are often included in such gels to prevent them drying out.
Na-CMC (Sodium carboxymethyl cellulose) is also used in self-adhesive ostomy, wound care, and dermatological patches as a muco-adhesive and to absorb wound exudate or transepidermal water and sweat.

This muco-adhesive property is used in products designed to prevent post-surgical tissue adhesions; and to localize and modify the release kinetics of active ingredients applied to mucous membranes; and for bone repair.
Encapsulation with carboxymethylcellulose sodium can affect drug protection and delivery.
There have also been reports of its use as a cyto-protective agent.

Na-CMC (Sodium carboxymethyl cellulose) is also used in cosmetics, toiletries, surgical prosthetics, and incontinence, personal hygiene, and food products.
Na-CMC (Sodium carboxymethyl cellulose) is one of the most significant byproducts of cellulose ethers which are created by natural cellulose modification as a type of cellulose derivate with an ether structure.
Termed Na-CMC (Sodium carboxymethyl cellulose), this polymer has a poor water solubility of the acid form of CMC and is typically preserved as sodium carboxymethylcellulose.

Na-CMC (Sodium carboxymethyl cellulose) is utilized in numerous industries and is referred to as monosodium glutamate in the workplace.
Na-CMC (Sodium carboxymethyl cellulose) is an offshoot of CMC.
Na-CMC (Sodium carboxymethyl cellulose) is a crucial by-product of cellulose ethers and is typically created by altering natural cellulose.

Since the Na-CMC (Sodium carboxymethyl cellulose) compound is typically poorly soluble in water, sodium CMC can be used to preserve it.
Na-CMC (Sodium carboxymethyl cellulose) has dispersibility and is soluble in cold water.
Emulsifying dispersion and solid dispersion are two of sodium Na-CMC (Sodium carboxymethyl cellulose)'s peculiar chemical properties.

Na-CMC (Sodium carboxymethyl cellulose) can be categorized as a derivative of a natural polymer.
Na-CMC (Sodium carboxymethyl cellulose), one of major cellulosic ethers, is widely used as a binding, thickening and stabilising agent (Lee et al. 2018).
Pharmaceutical grades of Na-CMC (Sodium carboxymethyl cellulose) are available commercially at degree of substitution (DS) values of 0.7, 0.9, and 1.2, with a corresponding sodium content of 6.5%–12% wt.

Na-CMC (Sodium carboxymethyl cellulose) is also available in several different viscosity grades.
Na-CMC (Sodium carboxymethyl cellulose) is highly soluble in water at all temperatures, forming clear solutions.
Na-CMC (Sodium carboxymethyl cellulose)s solubility depends on its degree of substitution.

Na-CMC (Sodium carboxymethyl cellulose) is an anionic water-soluble polymer based on renewable cellulosic raw material.
Na-CMC (Sodium carboxymethyl cellulose) functions as a rheology modifier, binder, dispersant, and an excellent film former.
These attributes make Na-CMC (Sodium carboxymethyl cellulose) a preferred choice as a bio-based hydrocolloid in multiple applications.

Na-CMC (Sodium carboxymethyl cellulose) acts as a thickener, binder, stabilizer, suspending agent and flow controlling agent.
Na-CMC (Sodium carboxymethyl cellulose) forms fine films that are resistant to oils, greases, and organic solvents.
Na-CMC (Sodium carboxymethyl cellulose) dissolves rapidly in cold water. 4) Acts as a protective colloid reducing water losses.

Na-CMC (Sodium carboxymethyl cellulose) is suitable for use in food systems.
Na-CMC (Sodium carboxymethyl cellulose) is physiologically inert.
Na-CMC (Sodium carboxymethyl cellulose) is an anionic polyelectrolyte.

Na-CMC (Sodium carboxymethyl cellulose) is a family of chemically modified cellulose derivatives containing the carboxymethyl ether group (-O-CH2-COO-) bound to some of the hydroxyl groups of the glucopyranose monomers that make up the cellulose backbone.
When Carboxymethylcellulose is recovered and presented as the Sodium salt, the resulting polymer is what is known as Na-CMC (Sodium carboxymethyl cellulose), and has the general chemical formula, [C6H7O2(OH)x(OCH2COONa)y]n.

Na-CMC (Sodium carboxymethyl cellulose) was discovered shortly after Word War 1 and has been produced commercially since the early 1930s.
Na-CMC (Sodium carboxymethyl cellulose) is produced by treating cellulose with an aqueous sodium hydroxide solution followed by monochloroacetic acid or its sodium salt.
In a parallel reaction two by-products, sodium chloride and sodium glycolate, are produced.

Once these by-products are removed, high purity Sodium carboxymethylcellulose is obtained.
As a general rule, the obtained material has a slight excess of sodium hydroxide and has to be neutralised.
The neutralisation endpoint can affect the properties of the material.

In the final step, the material is dried, milled to the desired particle size, and packaged.
Na-CMC (Sodium carboxymethyl cellulose), often abbreviated as Na-CMC or simply CMC, is a versatile and widely used chemical compound.

Na-CMC (Sodium carboxymethyl cellulose) is derived from cellulose, a natural polymer found in the cell walls of plants.
Na-CMC (Sodium carboxymethyl cellulose) is a water-soluble polymer and is used for a variety of purposes in various industries, including food, pharmaceuticals, cosmetics, and more.

Melting point: 274 °C (dec.)
Density: 1,6 g/cm3
FEMA: 2239 | CARBOXYMETHYLCELLULOSE
storage temp.: room temp
solubility: H2O: 20 mg/mL, soluble
form: low viscosity
pka: 4.30(at 25℃)
color: White to light yellow
Odor: Odorless
PH Range: 6.5 - 8.5
PH: pH (10g/l, 25℃) 6.0～8.0
Viscosity: 900 to 1400 mPa-s(1 %, H2O, 25 ℃)
Water Solubility: soluble
Merck: 14,1829

Alkali cellulose is prepared by steeping cellulose obtained from wood pulp or cotton fibers in sodium hydroxide solution.
The alkaline cellulose is then reacted with sodium monochloroacetate to produce Na-CMC (Sodium carboxymethyl cellulose).
Sodium chloride and sodium glycolate are obtained as by-products of this etherification.

Na-CMC (Sodium carboxymethyl cellulose) is used warm water or cold water when preparing the solution, and stir till it completely melts.
The amout of added water depends on variety and the use of multiple requirements.
High viscosity Na-CMC (Sodium carboxymethyl cellulose) is a white or slightly yellow fibrous powder, hygroscopic, odorless, tasteless, non-toxic, easy to ferment, insoluble in acids, alcohols and organic solvents, easily dispersed to form colloidal solution in water.

Na-CMC (Sodium carboxymethyl cellulose) is reacted by the acid and fibrous cotton, it is mainly used for water-based drilling fluids tackifier, it has certain role of fluid loss, it has strong salt and temperature resistance especially.
Na-CMC (Sodium carboxymethyl cellulose) is incompatible with strongly acidic solutions and with the soluble salts of iron and some other metals, such as aluminum, mercury, and zinc.

Na-CMC (Sodium carboxymethyl cellulose) is also incompatible with xanthan gum.
Precipitation may occur at pH < 2, and also when it is mixed with ethanol (95%).
Na-CMC (Sodium carboxymethyl cellulose) forms complex coacervates with gelatin and pectin.

Na-CMC (Sodium carboxymethyl cellulose) also forms a complex with collagen and is capable of precipitating certain positively charged proteins.
Food and pharmaceutical grade Carboxymethylcellulose is required by law to contain not less than 99.5% pure Na-CMC (Sodium carboxymethyl cellulose) and a maximum of 0.5% of residual salts (sodium chloride and sodium glycolate).

The degree of substitution (DS) can vary between 0.2-1.5, although it is generally in the range of 0.6-0.95.
The DS determines the behaviour of Na-CMC (Sodium carboxymethyl cellulose) in water: Grades with DS >0.6 form colloidal solutions in water that are transparent and clear, i.e the higher the content of carboxymethyl groups, the higher the solubility and smoother the solutions obtained.
Na-CMC (Sodium carboxymethyl cellulose) with a DS below 0.6 tends to be only partially soluble.

Na-CMC (Sodium carboxymethyl cellulose) is available as a white to almost white, odourless, tasteless, granular powder.
Na-CMC (Sodium carboxymethyl cellulose) is an anionic polymer with a clarified solution dissolved in cold or hot water.
Na-CMC (Sodium carboxymethyl cellulose) functions as a thickening rheology modifier, moisture retention agent, texture/body building agent, suspension agent, and binding agent in personal products and toothpaste.

Na-CMC (Sodium carboxymethyl cellulose) is desirable because the catalysis product (glucose) is easily measured using a reducing sugar assay, such as 3,5-dinitrosalicylic acid.
Using Na-CMC (Sodium carboxymethyl cellulose) in enzyme assays is especially important in screening for cellulase enzymes that are needed for more efficient cellulosic ethanol conversion.
Na-CMC (Sodium carboxymethyl cellulose) was misused in early work with cellulase enzymes, as many had associated whole cellulase activity with CMC hydrolysis.

Na-CMC (Sodium carboxymethyl cellulose) is one of the most important products of cellulose ethers, which are formed by natural cellulose modification as a kind of cellulose derivate with an ether structure.
Due to the fact that the acid form of Na-CMC (Sodium carboxymethyl cellulose) has poor water solubility, it is usually preserved as sodium carboxymethylcellulose, which is widely used in many industries and regarded as monosodium glutamate in industry.

Na-CMC (Sodium carboxymethyl cellulose) is used in cigarette adhesive, fabric sizing, footwear paste meal, home slimy.
Na-CMC (Sodium carboxymethyl cellulose) is used in interior painting architectural, building lines melamine, thickening mortar, concrete enhancement.
Na-CMC (Sodium carboxymethyl cellulose) is synthesized by the alkali-catalyzed reaction of cellulose with chloroacetic acid.

The polar (organic acid) carboxyl groups render the cellulose soluble and chemically reactive.
Fabrics made of cellulose—e.g. cotton or viscose rayon—may also be converted into Na-CMC (Sodium carboxymethyl cellulose).
Following the initial reaction, the resultant mixture produces approximately 60% Na-CMC (Sodium carboxymethyl cellulose) and 40% salts (sodium chloride and sodium glycolate); this product is the so-called technical CMC, which is used in detergents.

An additional purification process is used to remove salts to produce pure Na-CMC (Sodium carboxymethyl cellulose), which is used for alimentary and pharmaceutical applications.
An intermediate "semi-purified" grade is also produced, typically used in paper applications such as the restoration of archival documents.
Na-CMC (Sodium carboxymethyl cellulose) is a kind of cellulose widely used and used in the world today.

Na-CMC (Sodium carboxymethyl cellulose), is a cellulose derivative with 100-2000 degree of polymerization of glucose, and its relative molecular weight is 242.16.
White fibrous or granular powder.
Na-CMC (Sodium carboxymethyl cellulose) is odourless, tasteless, tasteless, hygroscopic and insoluble in organic solvents.

Na-CMC (Sodium carboxymethyl cellulose) is used as a thickener in the food industry, as a drug carrier in the pharmaceutical industry, as a binder and anti-retrogradation agent in the daily chemical industry.
Na-CMC (Sodium carboxymethyl cellulose) is a water-soluble polymer derived from cellulose through a chemical modification process.

Carboxymethyl groups (-CH2-COOH) are introduced into the cellulose structure.
These carboxymethyl groups make the cellulose molecule more water-soluble and provide it with its unique properties.
The viscosity of Na-CMC (Sodium carboxymethyl cellulose) solutions can be controlled by adjusting the concentration of the polymer.

This property makes it suitable for a wide range of applications, from thin solutions in beverages to thick gels in some pharmaceutical formulations.
Na-CMC (Sodium carboxymethyl cellulose) is stable over a wide pH range, making it suitable for use in both acidic and alkaline environments.
This is particularly important in the food industry where it can be used in a variety of products with different pH levels.

Na-CMC (Sodium carboxymethyl cellulose) is generally considered safe for consumption and topical use.
Na-CMC (Sodium carboxymethyl cellulose) is non-toxic and non-allergenic, which contributes to its widespread use in food and pharmaceutical products.
Na-CMC (Sodium carboxymethyl cellulose) is highly hydrophilic, meaning it has a strong affinity for water.

This property is useful in many applications where moisture retention or water binding is required.
Na-CMC (Sodium carboxymethyl cellulose) disperses easily in cold water, forming a smooth, uniform solution, which is advantageous in manufacturing processes.
Na-CMC (Sodium carboxymethyl cellulose) can be used to form films or coatings.

Na-CMC (Sodium carboxymethyl cellulose) can be used to create edible films for various purposes, such as encapsulating flavors or improving food packaging.
Na-CMC (Sodium carboxymethyl cellulose) is cost-effective and environmentally friendly because it is derived from renewable resources, such as wood pulp or cotton cellulose.
Na-CMC (Sodium carboxymethyl cellulose) is used as a highly effective additive to improve the product and processing properties in various fields of application - from foodstuffs, cosmetics and pharmaceuticals to products for the paper and textile industries.

History:
Na-CMC (Sodium carboxymethyl cellulose) was first obtained in 1918 by the German and is granted a patent in 1921.
Na-CMC (Sodium carboxymethyl cellulose) to achieve commercial production since 1921 in Europe.
But Na-CMC (Sodium carboxymethyl cellulose) was only for the crude product which was used as colloid and binder.

From 1936 to 1941, the industrial applied research of Na-CMC (Sodium carboxymethyl cellulose) is very active, people invented several enlightening patents.
German use Na-CMC (Sodium carboxymethyl cellulose) for synthetic detergent during World War II.

In 1943, Na-CMC (Sodium carboxymethyl cellulose) was first made by Hercules Company in the United States and produced the refined product’s sodium in 1946 which are recognized as safe food ingredients.
Now, Na-CMC (Sodium carboxymethyl cellulose) is the most widely used and the largest amount of fiber in the worlds.

Synthesis:
Na-CMC (Sodium carboxymethyl cellulose) is formed when cellulose reacts with mono chloroacetic acid or its sodium salt under alkaline condition with presence of organic solvent, hydroxyl groups substituted by Sodium carboxymethyl groups in C2, C3 and C6 of glucose, which substitution slightly prevails at C2 position.
Generally, there are two steps in manufacturing process of Na-CMC (Sodium carboxymethyl cellulose), alkalinization and etherification.

Step 1: Alkalinization
Disperse the raw material cellulose pulp in alkali solution (generally sodium hydroxide, 5–50%) to obtain alkali cellulose.
Cell-OH+NaOH →Cell·O-Na+ +H2O

Step 2: Etherification
Etherification of alkali cellulose with sodium monochloroacetate (up to 30%) in an alcohol-water medium.
The mixture of alkali cellulose and reagent is heated (50–75°C) and stirred during the process.
ClCH2COOH+NaOH→ClCH2COONa+H2O

Cell·O-Na+ +ClCH2COO- →Cell-OCH2COO-Na
The DS of the sodium CMC can be controlled by the reaction conditions and use of organic solvents (such as isopropanol).

Uses:
Na-CMC (Sodium carboxymethyl cellulose) is frequently called simply carboxymethyl cellulose and also known as cellulose gum.
Na-CMC (Sodium carboxymethyl cellulose) is derived from purified cellulose from cotton and wood pulp.
Na-CMC (Sodium carboxymethyl cellulose) is a water dispersible sodium salt of carboxy-methyl ether of cellulose that forms a clear colloidal solution.

Na-CMC (Sodium carboxymethyl cellulose) is a hygroscopic material that has the ability to absorb more than 50% of water at high humidity.
Na-CMC (Sodium carboxymethyl cellulose) is also a natural polymeric derivative that can be used in detergents, food and textile industries.
Na-CMC (Sodium carboxymethyl cellulose) can be used as a binder in the preparation of graphene nano-platelet based inks for the fabrication of dye sensitized solar cells (DSSCs).

Na-CMC (Sodium carboxymethyl cellulose) can also be used as a viscosity enhancer in the development of tyrosinase based inks for the formation of electrodes for biosensor applications.
Na-CMC (Sodium carboxymethyl cellulose) is used as a support material for a variety of cathodes and anodes for microbial fuel cells.
Na-CMC (Sodium carboxymethyl cellulose) is used in refractory fiber, ceramic production molding bond.

Na-CMC (Sodium carboxymethyl cellulose) is used in oil drilling, exploration address slurry thickening, reducing water loss, quality paper surface sizing.
Na-CMC (Sodium carboxymethyl cellulose) can be used as soap and washing powder detergent active additives, as well as other industrial production on the dispersion, emulsification, stability, suspension, film, paper, polishing and the like.
Quality product can be used for toothpaste, medicine, food and other industrial sectors.

Na-CMC (Sodium carboxymethyl cellulose) is resistant to bacterial decomposition and provides a product with uniform viscosity.
Na-CMC (Sodium carboxymethyl cellulose) can prevent skin moisture loss by forming a film on the skin’s surface, and also help mask odor in a cosmetic product.
Constituents are any of several fibrous substances consisting of the chief part of a plant’s cell walls (often extracted from wood pulp or cotton).

Na-CMC (Sodium carboxymethyl cellulose) salt is used in drilling muds, in detergents as a soil-suspending agent, in resin emulsion paints, adhesives, printing inks, textile sizes and protective colloid.
Na-CMC (Sodium carboxymethyl cellulose) acts as a stabilizer in foods.
Na-CMC (Sodium carboxymethyl cellulose) is also employed in pharmaceuticals as a suspending agent and excipients for tablets.

Na-CMC (Sodium carboxymethyl cellulose) is used as viscosity modifiers to stabilize the emulsions.
Na-CMC (Sodium carboxymethyl cellulose) is used as a lubricant in artificial tears and it is used to characterize enzyme activity from endoglucanases.
Na-CMC (Sodium carboxymethyl cellulose) is used in a variety of applications ranging from food production to medical treatments.

Na-CMC (Sodium carboxymethyl cellulose) is commonly used as a viscosity modifier or thickener, and to stabilize emulsions in various products, both food and non-food.
Na-CMC (Sodium carboxymethyl cellulose) is used primarily because it has high viscosity, is nontoxic, and is generally considered to be hypoallergenic, as the major source fiber is either softwood pulp or cotton linter.
Non-food products include products such as toothpaste, laxatives, diet pills, water-based paints, detergents, textile sizing, reusable heat packs, various paper products, filtration materials, synthetic membranes, wound healing applications, and also in leather crafting to help burnish edges.

Na-CMC (Sodium carboxymethyl cellulose) is used in food under the E number E466 or E469 (when it is enzymatically hydrolyzed), as a viscosity modifier or thickener, and to stabilize emulsions in various products, including ice cream.
Na-CMC (Sodium carboxymethyl cellulose) is also used extensively in gluten-free and reduced-fat food products.
Na-CMC (Sodium carboxymethyl cellulose) is used to achieve tartrate or cold stability in wine, an innovation that may save megawatts of electricity used to chill wine in warm climates.

Na-CMC (Sodium carboxymethyl cellulose) is more stable than metatartaric acid and is very effective in inhibiting tartrate precipitation.
Na-CMC (Sodium carboxymethyl cellulose) is reported that KHT crystals, in presence of CMC, grow slower and change their morphology.
Their shape becomes flatter because they lose 2 of the 7 faces, changing their dimensions.

Na-CMC (Sodium carboxymethyl cellulose) molecules, negatively charged at wine pH, interact with the electropositive surface of the crystals, where potassium ions are accumulated.
The slower growth of the crystals and the modification of their shape are caused by the competition between Na-CMC (Sodium carboxymethyl cellulose) molecules and bitartrate ions for binding to the KHT crystals.
Na-CMC (Sodium carboxymethyl cellulose) powder is widely used in the ice cream industry, to make ice creams without churning or extremely low temperatures, thereby eliminating the need for conventional churners or salt ice mixes.

Na-CMC (Sodium carboxymethyl cellulose) is used in baking breads and cakes.
The use of Na-CMC (Sodium carboxymethyl cellulose) gives the loaf an improved quality at a reduced cost, by reducing the need of fat.
Na-CMC (Sodium carboxymethyl cellulose) is also used as an emulsifier in biscuits.

By dispersing fat uniformly in the dough, it improves the release of the dough from the moulds and cutters, achieving well-shaped biscuits without any distorted edges.
Na-CMC (Sodium carboxymethyl cellulose) can also help to reduce the amount of egg yolk or fat used in making the biscuits.
Use of Na-CMC (Sodium carboxymethyl cellulose) in candy preparation ensures smooth dispersion in flavor oils, and improves texture and quality.

Na-CMC (Sodium carboxymethyl cellulose) is used in chewing gums, margarines and peanut butter as an emulsifier.
Na-CMC (Sodium carboxymethyl cellulose) has been used extensively to characterize enzyme activity from endoglucanases (part of the cellulase complex); it is a highly specific substrate for endo-acting cellulases, as its structure has been engineered to decrystallize cellulose and create amorphous sites that are ideal for endoglucanase action.

Na-CMC (Sodium carboxymethyl cellulose) is used as a soil suspension polymer designed to deposit onto cotton and other cellulosic fabrics, creating a negatively charged barrier to soils in the wash solution.
Na-CMC (Sodium carboxymethyl cellulose) is also used as a thickening agent, for example, in the oil-drilling industry as an ingredient of drilling mud, where it acts as a viscosity modifier and water retention agent.

Na-CMC (Sodium carboxymethyl cellulose) is sometimes used as an electrode binder in advanced battery applications (i.e. lithium ion batteries), especially with graphite anodes.
Na-CMC (Sodium carboxymethyl cellulose)'s water solubility allows for less toxic and costly processing than with non-water-soluble binders, like the traditional polyvinylidene fluoride (PVDF), which requires toxic n-methylpyrrolidone (NMP) for processing.
Na-CMC (Sodium carboxymethyl cellulose) is often used in conjunction with styrene-butadiene rubber (SBR) for electrodes requiring extra flexibility, e.g. for use with silicon-containing anodes.

Na-CMC (Sodium carboxymethyl cellulose) is also used in ice packs to form a eutectic mixture resulting in a lower freezing point, and therefore more cooling capacity than ice.
Aqueous solutions of Na-CMC (Sodium carboxymethyl cellulose) have also been used to disperse carbon nanotubes, where the long Na-CMC (Sodium carboxymethyl cellulose) molecules are thought to wrap around the nanotubes, allowing them to be dispersed in water.
In conservation-restoration, Na-CMC (Sodium carboxymethyl cellulose) is used as an adhesive or fixative (commercial name Walocel, Klucel).

Apart from the question of what is Na-CMC (Sodium carboxymethyl cellulose), their uses are also very important to know.
Na-CMC (Sodium carboxymethyl cellulose) can be used as a flocculant, chelator, emulsifier, thickener, water-retentive, sizing, and film-forming substance, among other things.
Electronics, pesticides, leather, plastics, printing, ceramics, and the daily-use chemical industry are just a few of the industries that heavily utilize Na-CMC (Sodium carboxymethyl cellulose).

Additionally, Na-CMC (Sodium carboxymethyl cellulose) has a wide range of applications due to its excellent properties, widespread use, and emerging potential fields.
Na-CMC (Sodium carboxymethyl cellulose) used as sizing agent and printing paste in printing and dyeing industry.
Na-CMC (Sodium carboxymethyl cellulose) can be used as a component of oil recovery fracturing fluid in the petrochemical industry.

Na-CMC (Sodium carboxymethyl cellulose) is a widely used ionic cellulose ether, widely used in petroleum, food, medicine, construction and ceramics industries, so it is also known as "industrial monosodium glutamate".
Na-CMC (Sodium carboxymethyl cellulose) is frequently used as a thickening agent in a wide range of food products, such as salad dressings, sauces, and ice cream.
Na-CMC (Sodium carboxymethyl cellulose) imparts viscosity and helps to stabilize these products.

Na-CMC (Sodium carboxymethyl cellulose) acts as a stabilizer and prevents ingredients from separating in products like beverages, including soft drinks and fruit juices.
In salad dressings, Na-CMC (Sodium carboxymethyl cellulose) helps create stable emulsions of oil and water, preventing them from separating.
In the pharmaceutical industry, Na-CMC (Sodium carboxymethyl cellulose) can be used as a binder in tablet formulations to hold the ingredients together.

In oral suspensions and liquid medications, Na-CMC (Sodium carboxymethyl cellulose) helps to suspend solid particles uniformly in the liquid, ensuring consistent dosing.
In cosmetics and personal care products, Na-CMC (Sodium carboxymethyl cellulose) can be used to improve the moisture retention properties of creams and lotions.
Na-CMC (Sodium carboxymethyl cellulose) is used in paper manufacturing to coat the surface of paper, improving its printability and smoothness.

In the oil and gas industry, Na-CMC (Sodium carboxymethyl cellulose) can be used in drilling fluids to control viscosity and fluid loss.
Na-CMC (Sodium carboxymethyl cellulose) is sometimes used in the textile industry as a sizing agent to improve the weaving process.
For its thickening and swelling properties, Na-CMC (Sodium carboxymethyl cellulose) is used in a variety of intricately formulated products for the pharmaceutical, food, home, and personal care industries as well as the paper, water treatment, and mineral processing industries.

Thorough knowledge of the concentration-dependent rheology and relaxation response is required to design Na-CMC (Sodium carboxymethyl cellulose) solutions for applications.
Alkali cellulose and sodium chloroacetate react to form a gummy substance that is either soluble in water or swells in water.
Na-CMC (Sodium carboxymethyl cellulose) is primarily used as a thickening, emulsifying, and stabilizing agent (as in sizes for textiles and paper and pharmaceutical ointments) as well as a bulk laxative and antacid in medicine.

Safety Profile:
Na-CMC (Sodium carboxymethyl cellulose) is used in oral, topical, and some parenteral formulations.
Na-CMC (Sodium carboxymethyl cellulose) is also widely used in cosmetics, toiletries, and food products, and is generally regarded as a nontoxic and nonirritant material.
However, oral consumption of large amounts of Na-CMC (Sodium carboxymethyl cellulose) can have a laxative effect; therapeutically, 4–10 g in daily divided doses of the medium- and high-viscosity grades of carboxymethylcellulose sodium have been used as bulk laxatives.

The WHO has not specified an acceptable daily intake for Na-CMC (Sodium carboxymethyl cellulose) as a food additive since the levels necessary to achieve a desired effect were not considered to be a hazard to health.
However, in animal studies, subcutaneous administration of Na-CMC (Sodium carboxymethyl cellulose) has been found to cause inflammation, and in some cases of repeated injection fibrosarcomas have been found at the site of injection.
Hypersensitivity and anaphylactic reactions have occurred in cattle and horses, which have been attributed to Na-CMC (Sodium carboxymethyl cellulose)m in parenteral formulations such as vaccines and penicillins.

Storage:
Na-CMC (Sodium carboxymethyl cellulose) is a stable, though hygroscopic material. Under high-humidity conditions, carboxymethylcellulose sodium can absorb a large quantity (>50%) of water.
In tablets, this has been associated with a decrease in tablet hardness and an increase in disintegration time.
Aqueous solutions are stable at pH 2–10; precipitation can occur below pH 2, and solution viscosity decreases rapidly above pH 10.

Generally, solutions exhibit maximum viscosity and stability at pH 7–9.
Na-CMC (Sodium carboxymethyl cellulose) may be sterilized in the dry state by maintaining it at a temperature of 1608℃ for 1 hour.
However, this process results in a significant decrease in viscosity and some deterioration in the properties of solutions prepared from the sterilized material.

Synonyms:
SODIUM CARBOXYMETHYL CELLULOSE
9004-32-4
sodium;2,3,4,5,6-pentahydroxyhexanal;acetate
Carboxymethylcellulose sodium (USP)
Carboxymethylcellulose cellulose carboxymethyl ether
CMC powder
Celluvisc (TN)
Carmellose sodium (JP17)
CHEMBL242021
C.M.C. (TN)
CHEBI:31357
E466
Sodium carboxymethyl cellulose (MW 250000)
D01544

Nansa HS 80/NPF is a series of organic compounds with the formula C12H25C6H4SO3Na.
Nansa HS 80/NPF is a colorless salt with beneficial properties as a surfactant.
Nansa HS 80/NPF is usually produced as a mixture of related sulfonates.

CAS Number: 11067-82-6
Molecular Formula: C18H21NaO3S
Molecular Weight: 340.41231
EINECS Number: 2342891

Nansa HS 80/NPF is a highly active anionic surfactant especially suitable for wetting, detergency and emulsification.
Nansa HS 80/NPF is used in a wide range of applications, including laundry detergents, surface cleaners and sanitary blocks.
The physical form allows direct incorporation into powders, compressed tablets and blocks.

Nansa HS 80/NPF is an important component of laundry detergent.
Nansa HS 80/NPF is a member of linear alkylbenzenesulfonates, that is, a member of the dodecyl group (C12H25).
Nansa HS 80/NPF is added at position 4 of the benzenesulfonate group.

Nansa HS 80/NPF can exist as six isomers based on the carbon of the dodecyl group (ignoring optical isomers).
Nansa HS 80/NPF, e.g. Derivatives from tetramerized propylene are also known (bottom right) but not as widely used.
Further complicating the definition of commercial materials, sodium dodecylbenzenesulfonate is a component of a compound.

Nansa HS 80/NPF has a mixture of compounds with varying alkyl chain lengths, mainly ranging from C10 to C16.
Nansa HS 80/NPF is considered representative of the entire class of compounds due to its average alkyl carbon number.
Nansa HS 80/NPF has been prepared by many methods.

Most commonly, Nansa HS 80/NPF is alkylated with long chain monoalkenes (eg dodecene) using hydrogen fluoride.
Nansa HS 80/NPF (and related derivatives) are then sulfonated with sulfur trioxide to give the sulfonic acid.
Nansa HS 80/NPF is then neutralized with sodium hydroxide.

Nansa HS 80/NPF surfactants are intended for industrial applications, primarily construction, paint, ink and emulsion polymerization.
Nansa HS 80/NPF acts as intermediates necessary to create specific end-use properties; It is used for foaming and detergent properties of mortar and plaster.
Nansa HS 80/NPF is a dried sodium C10-13 alkylbenzene sulfonate.

Nansa HS 80/NPF is a highly active anionic surfactant, providing excellent emulsification, wetting and detergent properties.
Nansa HS 80/NPF is a class of anionic surfactants consisting of a hydrophilic sulfonate head group and a hydrophobic alkyl.
Nansa HS 80/NPF is a class of anionic surfactants consisting of a hydrophilic sulfonate head group and a hydrophobic head group.

Nansa HS 80/NPF are widely used synthetic detergents and are used in many personal care products (soaps, shampoo, toothpaste, etc.) and household care products (laundry detergent, dishwashing liquid, spray cleaner, etc.).
Nansa HS 80/NPF is used as a surfactant in industrial and household detergents and cleaners.

Nansa HS 80/NPF is used in the chemicals, polymers, photography and textile processing industries;
Nansa HS 80/NPF is also used in photochemicals and building materials.
Nansa HS 80/NPF is a class of surfactants in which alkylbenzene sulfonates are the anionic moiety and sodium is the anionic moiety.

The cationic moiety is basically anionic surfactant.
Since Nansa HS 80/NPF is a surfactant, it is used for cleaning purposes.
Nansa HS 80/NPF can react with both soft water and hard water.

Nansa HS 80/NPF is a rust preventive additive synthesized by sulfonation and neutralization of heavy alkyl benzene, and its emulsion performance is good.
Nansa HS 80/NPF, emulsified cutting oil, can be combined with other additives to be formulated in the wire cutting process.
Nansa HS 80/NPF acts as a surfactant in the ionic self-assembly reaction of cyclophan.

Nansa HS 80/NPF is an ionic surfactant.
Nansa HS 80/NPF is used to stabilize the dispersions of graphene nanoflakes (GNFs) during liquid preparation.
Nansa HS 80/NPF can also individually suspend single-walled carbon nanotubes in aqueous medium and also give well-resolved spectral properties.

Nansa HS 80/NPF is used to manufacture amperometric biosensors for glucose.
Nansa HS 80/NPF is a substituted aromatic compound.
Nansa HS 80/NPF is used in consumer products (such as laundry detergent), chemical synthesis and agriculture.

Nansa HS 80/NPF is a white to light yellow flake, granule or powder.
Nansa HS 80/NPF is water soluble.
Nansa HS 80/NPF urgent steps must be taken to limit its spread to the environment.

Nansa HS 80/NPF is used as a synthetic detergent.
Nansa HS 80/NPF is a yellow oil capable of forming strong flake-like crystals in hexagonal or rhombic shape.
Nansa HS 80/NPF has micro-toxicity and has been recognized as a safe chemical by the international safety organization.

Nansa HS 80/NPF can be used to clean fruit and tableware.b
Nansa HS 80/NPF is sodium alkylbenzene sulphonate powder based on a predominately straight chain C10-13 alkylbenzene (dodecylbenzene).
Nansa HS 80/NPF is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.

The physical form allows direct incorporation into powders, compressed tablets and blocks.
Nansa HS 80/NPF acts as a hydrotrope and can be used to increase the solubility of other compounds.
Nansa HS 80/NPF can react with both soft water and hard water.

Nansa HS 80/NPF, emulsified cutting oil, can be combined with other additives to be formulated in the wire cutting process.
Nansa HS 80/NPF acts as a surfactant in the ionic self-assembly reaction of cyclophan.
Nansa HS 80/NPF is an ionic surfactant.

Nansa HS 80/NPF was used to stabilize the dispersions of graphene nanoflakes (GNFs) during the preparation of the liquid.
Nansa HS 80/NPF can be used for cleaning fruit and tableware.
Nansa HS 80/NPF used in detergents has a branched chain structure (ABS) and a linear structure (LAS).

Nansa HS 80/NPF has a significant effect on granular contamination, protein contamination and oil contamination.
Nansa HS 80/NPF is better for removing granular contamination from natural fibers
Nansa HS 80/NPF, together with non-ionic surfactants, increases the cloud point of the solution and provides a clear liquid.

Provides additional control over foaming properties and performance at higher temperatures.
Nansa HS 80/NPF can also be used to reduce the viscosity of concentrated surfactants and formulations.
Nansa HS 80/NPF is a hydrotrope, solubilizer, coupling agent, cloud point depressant, viscosity reducer, anti-caking agent in powder form.

Nansa HS 80/NPF is used as coupling agents to dissolve water-insoluble and often incompatible functional components.
Nansa HS 80/NPF is used to dissolve complex formulations in water.
Nansa HS 80/NPF provides functions to stabilize solutions, change viscosity and cloud point, limit phase separation at low temperature.

Nansa HS 80/NPF is an amphiphilic substance consisting of both hydrophilic and hydrophobic functional groups.
The hydrophobic part of the molecule is an apolar segment substituted with benzene.
Nansa HS 80/NPF, polar portion of SODIUM CUMEN SULFONATE is an anionic sulfonate group accompanied by a counterion.

Nansa HS 80/NPF is produced by sulfonation of an aromatic hydrocarbon solvent (cumene).
The resulting aromatic Nansa HS 80/NPF is neutralized using a suitable base (eg sodium hydroxide) to produce the sulfonate or hydroxide.
Nansa HS 80/NPF is a 'pure' substance but is typically produced and transported at a level of 90-95% as granular solids.

Nansa HS 80/NPF is an anionic surfactant used in liquid and powder detergent formulations, heavy-duty cleaners, and water.
Nansa HS 80/NPF are prepared industrially by the sulfonation of linear alkylbenzenes (LABs), which can themselves be prepared in several ways.
In the most common Nansa HS 80/NPF is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst

The purified dodecylbenzenes (and related derivatives) are then sulfonated with sulfur trioxide to give the Nansa HS 80/NPF.
Nansa HS 80/NPF is subsequently neutralized with sodium hydroxide.
Nansa HS 80/NPF acts as a solubilizing agent, coupling agent and cloud point depressant.

This part of the name indicates the presence of a benzene ring (a six-membered carbon ring with alternating double bonds) that is sulfonated.
Nansa HS 80/NPF usually refers to the presence of a sulfonic acid group (SO3H) in the molecule.

Melting Point: >300 °C
Color: White to yellow
Form: Solid
Solubility: Solubility in water
LogP: 0,45
Exact Mass: 349.18133527
Monoisotopic Mass: 349.18133527
Topological Polar Surface Area: 51.8 Ų

Nansa HS 80/NPF is used in various applications due to its viscosity reducing properties.
Nansa HS 80/NPF is used as a coupling agent, solubilizer and anti-caking agent in powder detergents.
Nansa HS 80/NPF supports compatibility between various chemicals found in multi-component systems.

The use of chemicals in a wide variety of shampoos and dishwashing detergents is expected to boost the Nansa HS 80/NPF market.
Nansa HS 80/NPF is a hydrotope compound consisting of a hydrophilic portion and a hydrophobic portion, similar to surfactant.
Nansa HS 80/NPF has several advantages.

Nansa HS 80/NPF increases the solubility of less soluble organic substances; lowers the cloud point of the aqueous formula.
Nansa HS 80/NPF is used as a solubilizer and cloud point suppressant in wax cleaners, air mist piercing, laundry washing.
Nansa HS 80/NPF are a class of anionic surfactants, consisting of a hydrophilic sulfonate head-group and a hydrophobic alkylbenzene tail-group.

Nansa HS 80/NPF, they are one of the oldest and most widely used synthetic detergents and may be found in numerous personal-care products (soaps, shampoos, toothpaste etc.) and household-care products (laundry detergent, dishwashing liquid, spray cleaner etc.).
They were introduced in the 1930s in the form of branched Nansa HS 80/NPF.

Nansa HS 80/NPF is a water-soluble compound that is widely used in various fields, including medical, environmental, and industrial research.
Nansa HS 80/NPF is a versatile compound that has a wide range of applications due to its unique chemical structure and biological activity.

Uses
Nansa HS 80/NPF is used as a resin dispersant, felt detergent and deinking agent in the papermaking industry.
Nansa HS 80/NPF is used as an osmotic degreaser in the leather industry.
Nansa HS 80/NPF is used as an anti-blocking agent in the fertilizer industry.

Nansa HS 80/NPF is used in the cement industry as a gasifier or separately or in combination with components.
Nansa HS 80/NPF creates a stable dispersion system or emulsion that increases the surface tension between the various components in the emulsion.
Nansa HS 80/NPF has hydrophilic groups and lipophilic groups in its molecule.

Nansa HS 80/NPF is collected at the oil/water border.
Nansa HS 80/NPF can also reduce the interfacial tension and reduce the energy required to form the emulsion.
As a kind of anionic surfactant, Nansa HS 80/NPF has good surface activity and strong hydrophilicity.

Nansa HS 80/NPF effectively reduces oil and water surface tension due to emulsification.
Nansa HS 80/NPF is sodium alkylbenzene sulfonate powder based mainly on straight chain C10-13 alkylbenzene.
Nansa HS 80/NPF is a highly active anionic surfactant especially suitable for wetting, detergency and emulsification.

It has a wide range of applications, including laundry detergents, surface cleaners and sanitary blocks.
Nansa HS 80/NPF is a series of organic compounds with the formula C12H25C6H4SO3Na.
Nansa HS 80/NPF is a colorless salt with beneficial properties as a surfactant.

Nansa HS 80/NPF is usually produced as a mixture of related sulfonates.
Nansa HS 80/NPF is an important component of laundry detergent.
Nansa HS 80/NPF is considered representative of the entire class of compounds due to its average alkyl carbon number.

Nansa HS 80/NPF has been prepared by many methods.
Nansa HS 80/NPF is then neutralized with sodium hydroxide.
Nansa HS 80/NPF surfactants are intended for industrial applications, primarily construction, paint, ink and emulsion polymerization.

Nansa HS 80/NPF is a dried sodium C10-13 alkylbenzene sulfonate.
Nansa HS 80/NPF is a highly active anionic surfactant, providing excellent emulsification, wetting and detergent properties.
Nansa HS 80/NPF is a class of anionic surfactants consisting of a hydrophilic sulfonate head group and a hydrophobic alkyl.

Nansa HS 80/NPF is a class of anionic surfactants consisting of a hydrophilic sulfonate head group and a hydrophobic head group.
Nansa HS 80/NPF are widely used synthetic detergents and are used in many personal care products (soaps, shampoo, toothpaste, etc.) and household care products (laundry detergent, dishwashing liquid, spray cleaner, etc.).
Nansa HS 80/NPF is used as a surfactant in industrial and household detergents and cleaners.

Nansa HS 80/NPF is used in the chemicals, polymers, photography and textile processing industries;
Nansa HS 80/NPF is also used in photochemicals and building materials.
Nansa HS 80/NPF is a class of surfactants in which alkylbenzene sulfonates are the anionic moiety and sodium is the anionic moiety.

The cationic moiety is basically anionic surfactant.
Nansa HS 80/NPF is used in the following products: polymers, coating products, fillers, putties, plasters, modelling clay, paper chemicals and dyes and adhesives and sealants.
Nansa HS 80/NPF is used in the following areas: municipal supply (e.g. electricity, steam, gas, water) and sewage treatment, building & construction work and formulation of mixtures and/or re-packaging.

Nansa HS 80/NPF is used for the manufacture of: rubber products, pulp, paper and paper products and plastic products.
Release to the environment of Nansa HS 80/NPF 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), as processing aid, for thermoplastic manufacture and in the production of articles.

Nansa HS 80/NPF are often used in detergents and cleaning products due to their ability to lower the surface tension of water and enhance the removal of dirt, grease, and stains.
Nansa HS 80/NPF can act as emulsifiers and dispersants, helping to mix immiscible substances and stabilize emulsions in products like paints, coatings, and cosmetics.

Nansa HS 80/NPF can be used in dyeing and finishing processes in the textile industry, improving the dye absorption and colorfastness of fabrics.
Nansa HS 80/NPF are used as additives in lubricating oils and drilling fluids to improve their performance and stability under extreme conditions.
Nansa HS 80/NPF can be used in water treatment processes to remove heavy metals and other contaminants from industrial wastewater.

Nansa HS 80/NPF can be used as intermediates in the synthesis of pharmaceuticals and agrochemicals.
Nansa HS 80/NPF is used to modify ion exchange resins for applications such as water softening and purification.
Nansa HS 80/NPF is used in biological research as labeling agents or markers due to their fluorescent properties.

Safety
Nansa HS 80/NPF, especially those with surfactant properties, might cause skin or eye irritation upon contact.
They could also lead to allergic sensitization in some individuals.
Depending on the specific compound, there might be concerns about acute or chronic toxicity.

Ingestion, inhalation, or absorption through the skin of certain Nansa HS 80/NPF could potentially cause harm.
Nansa HS 80/NPF might have negative effects on aquatic ecosystems due to their surfactant properties, which can disrupt surface tension and affect aquatic organisms.
The extent of environmental impact would depend on factors like concentration and persistence in the environment.

The flammability of a Nansa HS 80/NPF would depend on its chemical structure.
Some organic compounds, including those containing carbon and hydrogen, can be flammable under certain conditions.

Synonyms
Tetrapropylenebenzyl sulfonate
Jadinol PU
Neogen R
Sodium tetrapropylbenzene sulfonate
11067-82-6
Merpisap PD82
TPBS
Nansa HS 55
EINECS 234-289-1
Sodium tetrapropylenebenzenesulphonate
Tetrapropylenebenenesulphonate, sodium salt
Benzenesulfonic acid, tetrapropylene-, sodium salt
sodium 2-dodecylbenzenesulfonate 3-dodecylbenzenesulfonate 4-dodecylbenzenesulfonate
Benzenesulfonic acid, tetrapropylene-, (3R-(3alpha,3aalpha,4beta,4abeta,7abeta,8alpha,9abeta))-
trisodium;2-dodecylbenzenesulfonate;3-dodecylbenzenesulfonate;4-dodecylbenzenesulfonate
AVWQQPYHYQKEIZ-UHFFFAOYSA-K
DTXSID601016230
AKOS040754173
LS-32078
Q15718771

DESCRIPTION:

NANSA HS 80/S is dried sodium C10-13 alkylbenzene sulfonate.
NANSA HS 80/S is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.
The physical form allows direct incorporation into powders, compressed tablets and blocks.

CAS No: 25155-30-0
INCI-NAME: Sodium Dodecylbenzene Sulfonate
Formula: C18H30O3S.Na

NANSA HS 80 / S is a dried sodium C10-13 alkylbenzene sulfonate.
NANSA HS 80 / S is highly active anionic surfactant, provides excellent emulisfication, wetting and detergent properties to a wide range of applications.
Sodium Dodecylbenzene Sulfonate ( contains Phosphate) has 80% active powder.
NANSA HS 80 / S is Non-vegetable.

NANSA HS 80 / S is Primary anionic surfactant.
NANSA HS 80 / S has Excellent foaming and detergency properties.
NANSA HS 80 / S is Chemically stable in acidic and alkaline conditions.



USE AND MANUFACTURING OF NANSA HS 80 / S
NANSA HS 80 / S is Used as textile printing and dyeing auxiliary
NANSA HS 80 / S is used as silk printing, penetration and degumming refining auxiliary
GB276-96 stipulates as processing auxiliary for food industry.
NANSA HS 80 / S is Anionic surfactant.
NANSA HS 80 / S has excellent foaming power and detergency.

Because of its low production cost and good performance, NANSA HS 80 / S has a wide range of uses.
NANSA HS 80 / S is the most used synthetic surfactant for household detergents.
NANSA HS 80 / S also produces some inorganic salts such as magnesium and calcium and organic amine salts such as triethanolamine.

NANSA HS 80 / S has excellent emulsifying properties and is an important part of mixed emulsifiers for various pesticides.
Benzene can be condensed with α-olefin under aluminum trichloride catalyst, and the condensed liquid can be washed with alkali and water, and then distilled to recover benzene, and vacuum distillation can obtain refined alkylbenzene.
Then it is sulfonated with fuming sulfuric acid and neutralized with white ash (in 2 times the amount of ethanol) to obtain calcium dodecylbenzene sulfonate


CHEMICAL AND PHYSICAL PROPERTIES OF NANSA HS 80/S:
PSA： 65.58000
XLogP3： 6.13490
Appearance：
white or light yellow flakes
Density： 1.02 g/cm3
Melting Point： >300 °C
Toxicity： LD50 in mice: 2 g/kg orally; 105 mg/kg i.v. (Hopper)
Molecular Weight：
348.47600
Exact Mass：
348.17400
HScode：
3402110000





SAFETY INFORMATION ABOUT NANSA HS 80/S:
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




SYNONYMS OF NANSA HS 80/S:
Benzenesulfonic acid,dodecyl-,sodium salt (1:1);
Benzenesulfonic acid,dodecyl-,sodium salt;
Sodium laurylbenzenesulfonate;
Stepan DS 60;
Ultrawet 1T;
Marlon A 350;
Sodium dodecylphenylsulfonate;
Sulframin 85;
Marlon A;
Dodecylbenzenesulfonic acid sodium salt;
Maranil;Marlon A 375;
Nacconol 35SL;
Siponate DS 10;
Trepolate F 40;
Conoco C 550;
KB (surfactant);
Nansa SL;
Santomerse Me;
Merpisap AP 90P;
Nansa SS;
Trepolate F 95;
Nansa HS 80;
Deterlon;
Ultrawet 99LS;
Sulfuril 50;F 90;
Elfan WA Powder;
Sandet 60;
Steinaryl NKS 50;
Sinnozon;
Nansa HS 85S;
C 550;
KB;
HS 85S;
Nansa HF 80;
Arylan SBC;
Marlon 375A;
X 2073;
Conco AAS 35H;
Neopelex 05;
Richonate 40B;
DS 60;
Pelopon A;
Sulframin 1240;
Richonate 1850;
35SL;
Calsoft L 40;
Calsoft F 90;
SDBS;
Alkanate DC;
Sulfaril Paste;
Steinaryl NKS 100;
Siponate DS 4;
Siponate LDS 10;
Nestapone;
Nansa 1260;
Marlon 375;
Neopelex F 60;
Abeson NAM;
Emulin B 22;
Neopelex 6;
Bio-Soft D 40;
Neogen SC;
Nissan Newrex R;
Conco AAS 35;
Reworyl NKS 50;
Elfan WA 35;
Neopelex 25;
Elfan WA 50;
MB-VR;
Marlon A 396;
Neopelex F 25;
Witconate 1238;
Sulframin 40;
Nacconol 40F;
Nansa HS 80S;
Conco AAS 45S;
Newrex R;
A 1-1575;
Nansa 1106;
Maranil A 55;
Neopelex 6E;
Liponox LE 110;
Nissan Newrex H;
Vista C 550;
Witconate 1250;
Conco AAS 40S;
Bio-Soft D 35X;
Stepantan DS 40;
Phenyl Sulfonate HSR;
Deterlon A;
Polystep A 15;
Nansa HS 80SA;
Bio-Soft LAS 40S;
Witconate 60B;
Nissan Newrex F;
Newrex Powder F;
F 90 (sulfonic acid);
Nansa SSA 055;
Newrex T;
1323-13-3;
11114-21-9;
12068-21-2;
12627-25-7;
12676-70-9;
18618-53-6;
19327-14-1;
28675-02-7;
37334-89-7;
39316-39-7;
39386-98-6;
39405-16-8;
52624-37-0;
56590-39-7;
57762-50-2;
58517-33-2;
60328-33-8;
63530-22-3;
68445-25-0;
71244-85-4;
76483-01-7;
82028-94-2;
82785-43-1;
83203-33-2;
83652-87-3;
83652-88-4;
83652-89-5;
88495-86-7;
90452-02-1;
94187-92-5;
122390-78-7;
128452-17-5;
138362-06-8;
142986-60-5;
147035-77-6;
167163-39-5;
170006-86-7;
177645-67-9;
178900-97-5;
189201-38-5;
254117-47-0;
295348-93-5;
312629-70-2;
352212-18-1

DESCRIPTION:
NANSA HS 85 / NPF is sodium alkylbenzene sulphonate powder based on a predominately straight chain C10-13 alkylbenzene (dodecylbenzene).
NANSA HS 85 / NPF is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.
The physical form allows direct incorporation into powders, compressed tablets and blocks.


CAS number: 85117-50-6
EC number: 285-600-2
PHYSICAL AND CHEMICAL PROPERTIES OF NANSA HS 85 / NPF:
Appearance:
Granules. Dusty powder. Solid
Colour Beige.
Odour Odourless.
pH pH (concentrated solution): 9 - 11 pH (diluted solution): 9 @ 1%
Relative density 400 - 500 @ @ 20˚C°C
Solubility(ies) Soluble in water.


SAFETY INFORMATION ABOUT NANSA HS 85 / NPF:
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

Nansa HS 85/NPF is a versatile chemical compound.
Nansa HS 85/NPF is a sodium alkylbenzene sulphonate powder.
The primary constituent of Nansa HS 85/NPF is straight-chain C10-13 alkylbenzene, specifically dodecylbenzene.
Nansa HS 85/NPF is classified as a high-active anionic surfactant.



APPLICATIONS


Nansa HS 85/NPF is widely used in laundry detergents to enhance their cleaning power.
Nansa HS 85/NPF effectively removes dirt, stains, and grime from clothing and fabrics.

Nansa HS 85/NPF is a key ingredient in many liquid laundry detergents.
Nansa HS 85/NPF is used in powder laundry detergents as well, improving their performance.
Nansa HS 85/NPF is used in the formulation of various surface cleaners for household and industrial use.

Nansa HS 85/NPF helps break down and remove grease, oils, and residues from surfaces.
Nansa HS 85/NPF is used in dishwashing detergents to enhance their degreasing capabilities.

Nansa HS 85/NPF is known for its ability to create stable emulsions of oil and water.
Nansa HS 85/NPF is incorporated into hygienic blocks, which are used for cleaning and deodorizing toilet bowls and urinals.

Nansa HS 85/NPF provides wetting properties in various cleaning solutions, ensuring even coverage on surfaces.
Nansa HS 85/NPF is used in the production of compressed tablets for dishwashing and laundry.
Nansa HS 85/NPF enhances the foaming and cleaning performance of detergents.

Nansa HS 85/NPF is employed in the formulation of industrial cleaners for equipment and machinery.
Nansa HS 85/NPF is used in car wash detergents to help remove road grime and dirt from vehicles.
Nansa HS 85/NPF finds applications in the manufacturing of degreasers and heavy-duty cleaning solutions.

Nansa HS 85/NPF contributes to the effectiveness of degreasing and descaling agents.
Nansa HS 85/NPF is used in the production of multi-purpose household cleaners.
Nansa HS 85/NPF helps maintain the stability of cleaning product formulations.

Nansa HS 85/NPF is employed in the formulation of degreasers for kitchen appliances and surfaces.
Nansa HS 85/NPF plays a role in the emulsification of fats and oils in industrial settings.
Nansa HS 85/NPF is added to cleaning solutions for floors, walls, and countertops.
Nansa HS 85/NPF can be used in the preparation of cleaning wipes and wet wipes.
Nansa HS 85/NPF is found in various formulations for institutional and commercial cleaning.

Nansa HS 85/NPF assists in achieving thorough and efficient cleaning results.
Nansa HS 85/NPF is a versatile ingredient, finding applications in a wide range of cleaning and detergent products.

Nansa HS 85/NPF is used in industrial degreasing processes to remove oil and grease from machinery parts.
Nansa HS 85/NPF aids in breaking down and dispersing stubborn residues on surfaces.
Nansa HS 85/NPF is incorporated into carpet cleaning solutions to help remove stains and dirt from carpets and upholstery.
Nansa HS 85/NPF is utilized in the production of concentrated liquid dishwashing detergents.

Nansa HS 85/NPF contributes to the formulation of high-performance glass and window cleaners.
Nansa HS 85/NPF is found in the manufacturing of specialty cleaning products for the food industry.

Nansa HS 85/NPF is used in the formulation of kitchen degreasers for both household and commercial use.
Nansa HS 85/NPF is added to floor cleaners to improve their ability to remove dirt and grime from various flooring types.

Nansa HS 85/NPF assists in the emulsification of oils in automotive engine cleaning products.
Nansa HS 85/NPF can be found in handwashing dish soap formulations.
Nansa HS 85/NPF is used in the production of disinfectant cleaners for surfaces.

Nansa HS 85/NPF helps in the removal of soap scum and mineral deposits in bathroom cleaners.
Nansa HS 85/NPF is employed in the formulation of mold and mildew removers for household and industrial applications.

Nansa HS 85/NPF is utilized in the production of all-purpose spray cleaners for convenience.
Nansa HS 85/NPF is added to laundry pre-treatment products designed to target tough stains.

Nansa HS 85/NPF is used in the formulation of stain removers for fabrics and carpets.
Nansa HS 85/NPF plays a role in the production of cleaning solutions for appliances like stovetops and ovens.
Nansa HS 85/NPF can be found in the composition of vehicle degreasing and cleaning products.

Nansa HS 85/NPF is employed in the creation of surface sanitizers and disinfectants.
Nansa HS 85/NPF assists in achieving streak-free shine in glass and mirror cleaning solutions.

Nansa HS 85/NPF is added to floor stripping and waxing products for industrial and commercial floor maintenance.
Nansa HS 85/NPF is used in the formulation of rust and corrosion removers.

Nansa HS 85/NPF can be found in the production of pool and spa cleaning solutions.
Nansa HS 85/NPF helps to create effective cleaning formulations for outdoor surfaces and decks.
Nansa HS 85/NPF's versatile properties make it a valuable component in various cleaning and maintenance products across industries.



DESCRIPTION


Nansa HS 85/NPF is a versatile chemical compound.
Nansa HS 85/NPF is a sodium alkylbenzene sulphonate powder.

The primary constituent of Nansa HS 85/NPF is straight-chain C10-13 alkylbenzene, specifically dodecylbenzene.
Nansa HS 85/NPF is classified as a high-active anionic surfactant.
Nansa HS 85/NPF is particularly well-suited for providing wetting properties.

Nansa HS 85/NPF is also known for its excellent detergency characteristics.
Nansa HS 85/NPF has strong emulsification capabilities.

Nansa HS 85/NPF finds application in a wide range of products.
This includes laundry detergents.

Nansa HS 85/NPF is used in surface cleaners as an effective cleaning agent.
Nansa HS 85/NPF is also used in the production of hygienic blocks.
Nansa HS 85/NPF is available in powder form.

Its physical form makes it easy to incorporate into various product formulations.
Nansa HS 85/NPF is highly active, meaning it can be used in relatively small quantities to achieve the desired effects.
Nansa HS 85/NPF helps to break down and remove dirt, stains, and grease from surfaces.
Nansa HS 85/NPF is suitable for both household and industrial cleaning applications.

Its emulsification properties make it useful for formulating products like dishwashing liquids.
Nansa HS 85/NPF enhances the dispersion of oil and grease in water-based solutions.
Nansa HS 85/NPF is compatible with other common detergent ingredients.

Nansa HS 85/NPF contributes to the foaming and cleaning performance of detergent formulations.
Nansa HS 85/NPF can be used in dry powder laundry detergents.

Nansa HS 85/NPF is also effective in concentrated liquid detergents.
Nansa HS 85/NPF helps maintain the stability of detergent formulations.

Nansa HS 85/NPF can be used in both manual and automatic washing machines.
Nansa HS 85/NPF is known for its effectiveness in removing tough stains and providing a high level of cleanliness.



PROPERTIES


Chemical Composition: Nansa HS 85/NPF primarily consists of straight-chain C10-13 alkylbenzene, specifically dodecylbenzene.
Chemical Formula: The specific chemical formula may not be disclosed for proprietary commercial products.
Physical Form: It is available in powder form.
Ionic Nature: Nansa HS 85/NPF is an anionic surfactant, meaning it carries a negative charge when dissolved in water.
Solubility: It is soluble in water, which is important for its use in aqueous cleaning solutions.
Wetting Properties: Nansa HS 85/NPF is known for its excellent wetting capabilities, ensuring thorough coverage of surfaces.
Detergency: It possesses strong detergency properties, aiding in the removal of dirt, stains, and grease.
Emulsification: Nansa HS 85/NPF is effective at emulsifying oils and grease, allowing them to mix with water-based solutions.
Foaming: It contributes to the foaming properties of cleaning products, creating lather in detergents and cleaners.
Compatibility: The chemical is compatible with a range of other detergent ingredients and additives.
Stability: It helps maintain the stability of cleaning product formulations, preventing separation or degradation.
Cleaning Performance: NANSA HS 85/NPF is recognized for its ability to provide high-quality cleaning and stain removal.



FIRST AID


Inhalation:

If inhaled, move the affected person to an area with fresh air immediately.
Allow the person to rest in a comfortable position and keep them warm.
If breathing difficulties persist or if there are signs of respiratory distress, seek immediate medical attention.


Skin Contact:

In case of skin contact, promptly remove contaminated clothing.
Wash the affected skin area gently but thoroughly with plenty of water and mild soap.
If skin irritation, redness, or rash develops, seek medical attention.
If the chemical is in powder form, carefully brush off excess powder before washing with water.


Eye Contact:

If the chemical comes into contact with the eyes, immediately rinse the affected eye(s) gently with lukewarm, running water for at least 15 minutes. Hold the eyelids open to ensure thorough rinsing.
Seek immediate medical attention if eye irritation or redness persists or if there is any discomfort.


Ingestion:

If Nansa HS 85/NPF is ingested, do not induce vomiting unless directed to do so by medical professionals.
Rinse out the mouth with water if the person is conscious and able to do so.
Seek immediate medical attention or contact a poison control center.
Provide the medical personnel with detailed information about the ingested substance.


In Case of Spills or Leaks:

Avoid direct contact with the spilled material.
Wear appropriate personal protective equipment (PPE) such as gloves, safety goggles, and protective clothing.
Contain the spill if possible, using absorbent materials like sand, vermiculite, or commercial spill control agents.
Carefully collect the spilled material and place it in suitable containers for disposal.
Ventilate the area to disperse any fumes or vapors.
Dispose of the spilled material and contaminated items in accordance with local regulations and guidelines.

Nansa HS 85/S is a substituted aromatic compound.
The chemical formula of Nansa HS 85/S is C18H29NaO3S and its molecular weight is 384.48.


CAS Number: 25155-30-0
EC Number: 246-680-4
MDL number: MFCD00011508
Linear Formula: CH3(CH2)11C6H4SO3Na
Molecular Formula: C18H29NaO3S
INCI-NAME: Sodium Dodecylbenzene Sulfonate


Nansa HS 85/S is a white or light yellow powder or flake solid.
Nansa HS 85/S is hard to volatilize, easily soluble in water, easy to absorb moisture and agglomerate, soluble in water to form a translucent solution.
Nansa HS 85/S is chemically stable to alkali, dilute acid and hard water, and can establish a balanced system with strong acid, which is slightly toxic.


The chemical formula of Nansa HS 85/S is C18H29NaO3S and its molecular weight is 384.48.
Nansa HS 85/S is a white or yellowish powder and is soluble in water.
Nansa HS 85/S is neutral, sensitive to the hardness of water, not easy to oxidation, strong foaming ability, high decontamination power, easy to mix various auxiliaries, low production cost and mature synthesis process.


Nansa HS 85/S has been recognized as a safe chemical raw material by international safety organizations and is an anionic surfactant.
Nansa HS 85/S is a series of organic compounds with the formula C12H25C6H4SO3Na.
Nansa HS 85/S is a colourless salt with useful properties as a surfactant.


Nansa HS 85/S is usually produced as a mixture of related sulfonates.
Nansa HS 85/S is a major component of laundry detergent.
Nansa HS 85/S is a white or light yellow flakes.


Nansa HS 85/S is a white to light yellow flakes, granules or powder.
Nansa HS 85/S is soluble in water.
Nansa HS 85/S is non flammable.


Nansa HS 85/S is a white or light yellow powder or flake solid.
Nansa HS 85/S is difficult to volatilize, but it easy to dissolve in water and become a subtransparent solution.
For alkali, dilute acid, Nansa HS 85/S has stable hard water properties.


According to the physicochemical property, Nansa HS 85/S has three main functions.
Nansa HS 85/S is dried sodium C10-13 alkylbenzene sulfonate.
Nansa HS 85/S is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.


The physical form of Nansa HS 85/S allows direct incorporation into powders, compressed tablets and blocks.
Nansa HS 85/S is a dried sodium C10-13 alkylbenzene sulfonate.
Nansa HS 85/S is a high active anionic sufactant particularly suited to provide wetting, detergency and emulsifcation in a wide range of applications.


Nansa HS 85/S is dried sodium C10-13 alkylbenzene sulfonate.
Nansa HS 85/S is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.


The physical form of Nansa HS 85/S allows direct incorporation into powders, compressed tablets and blocks.
Nansa HS 85/S is chemically stable in acidic and alkaline conditions.
Nansa HS 85/S is non-vegetable.


Nansa HS 85/S is a kind of yellow oily, micro-toxicity.
Nansa HS 85/S is neutral, more sensitive to water hardness, and not easy to oxidation.
Nansa HS 85/S has strong foaming ability and detergency and is easy to compound with various additives.


Nansa HS 85/S is a high-content anionic surfactant with detergency, moistening, foaming, emulsifying, and dispersing properties.
The biological degradability of Nansa HS 85/S is more than 90%.
International security organizations have recognized Nansa HS 85/S as a safe chemical.


Nansa HS 85/S is an efficient additive that can improve the quality of organic and inorganic chemical products that are easy to absorb moisture and agglomerate.
Nansa HS 85/S is a white or light yellow flakes



USES and APPLICATIONS of NANSA HS 85/S:
Nansa HS 85/S is widely used in the production of various detergents and emulsifiers, and can be properly used in cosmetics such as shampoo, foam bath, etc.
Nansa HS 85/S can also be used as cleaning agent in textile industry, dyeing assistant, degreasing agent in electroplating industry.
Nansa HS 85/S is a used deinking agent in the paper industry also needs to add a certain amount of sodium dodecylbenzene sulfonate.


In addition, linear alkylbenzene sulfonate is very stable to oxidizer and soluble in water, so Nansa HS 85/S is very suitable for washing powder with oxidizing bleach.
Nansa HS 85/S is a surfactant salt used in consumer products (such as laundry detergent), chemical synthesis, and agriculture.


Nansa HS 85/S is a surfactant used in proteomics research.
Nansa HS 85/S is a versatile anionic surfactant utilized in various laboratory and industrial settings.
Nansa HS 85/S is both biodegradable and non-toxic, offering a broad range of applications across fields like biochemistry, nanotechnology, and medical research.


Nansa HS 85/S's functions extend to emulsification, detergency, and cleaning purposes.
Nansa HS 85/S's role as an anionic surfactant aids in the solubilization of proteins, lipids, and other macromolecules.
Moreover, Nansa HS 85/S finds application in gel electrophoresis for the separation of proteins and macromolecules based on size.


Additionally, Nansa HS 85/S plays a crucial part in DNA sample preparation for sequencing and nanoparticle production.
As an anionic surfactant, Nansa HS 85/S reduces the surface tension of aqueous solutions, enabling the solubilization of proteins, lipids, and other macromolecules.


Nansa HS 85/S also interacts with proteins and macromolecules, modifying their shape and enhancing solubility.
Nansa HS 85/S is often used as a cotton fabric refining agent, desizing aid, and leveling agent during dyeing in textile auxiliaries.
Nansa HS 85/S is used as a metal degreasing agent in the metal electroplating process.


Nansa HS 85/S is used in the paper industry.
Nansa HS 85/S is used as resin Dispersant, felt detergent, deinking agent.
Nansa HS 85/S is used as penetrating degreasing agent in leather industry.


Nansa HS 85/S is used as anti-caking agent in fertilizer industry.
Nansa HS 85/S is used as AIR-entraining agent in cement industry and many other aspects or is used alone.
Nansa HS 85/S is used as an ingredient.


Nansa HS 85/S is used for detergents for household use, detergent and washing detergent for professional use, construction – air-entraining admixtures, emulsion polymerization, and plant protection products.
Nansa HS 85/S is a commonly used anionic surfactant.


Nansa HS 85/S is a surfactant used in proteomics research.
Nansa HS 85/S has been used to stabilize dispersions of graphene nanoflakes (GNFs) during the preparation of the liquid phase of GNFs.
Nansa HS 85/S can also suspend single-walled carbon nanotubes as individuals in aqueous media and also give well-resolved spectral features.


Nansa HS 85/S is used as an Anionic detergent.
Nansa HS 85/S is used as a synthetic detergent.
Therefore, Nansa HS 85/S has been widely used in the preparation of cosmetics, food, printing and dyeing auxiliaries and pesticides.


Nansa HS 85/S products are widely used.
In addition to the several functions, Nansa HS 85/S also can be used as a cotton fabric refining agent and desizing agent in textile.
Nansa HS 85/S is used as resin dispersant, felt detergent and deinking agent in the papermaking industry.


Nansa HS 85/S is used as an osmotic degreaser in the leather industry.
Nansa HS 85/S is used as an anti-blocking agent in the fertilizer industry.
Nansa HS 85/S is used in the cement industry as a gassing agent, or used separately or in conjunction with components.


In recent years, Nansa HS 85/S has often been used with nonionic surfactants such as fatty alcohol polyoxyethylene ether (AEO) for better washing effect.
The main purpose of Nansa HS 85/S is to make a variety detergents.
Nansa HS 85/S has a significant effect on the granular fouling, protein fouling, and oil fouling.


Nansa HS 85/S is better for cleaning granular fouling on natural fibers.
The detergency of Nansa HS 85/S is enhanced with the increase of temperature.
The effect on protein fouling is better than that of the non-ionic surfactant.


However, there are two disadvantages of sodium dodecyl benzene sulfonates, one is poor hard water tolerance and the detergency can be reduced with the hardness of the water.
Therefore, the detergent must be used with the appropriate chelating mixture.


Second, the decreasing ability is too strong.
Nansa HS 85/S can be used to clean fruit and tableware.
Nansa HS 85/S is used in detergent has a branched chain structure (ABS) and linear structure (LAS).


Nansa HS 85/S is commonly used as an anionic surfactant.
Nansa HS 85/S is used in detergent and has a branched chain structure (ABS) and linear structure (LAS).
The branched chain structure of Nansa HS 85/S has small biodegradability.


Nansa HS 85/S can cause environmental pollution.
The linear structure of Nansa HS 85/S is easier biodegradation more than 90%.
Nansa HS 85/S has little influence on the environment.


Nansa HS 85/S is used as an anionic detergent, as an emulsifier (emulsion polymerization, metalworking fluids), and as a surfactant (pesticides, textiles).
Nansa HS 85/S has been used in cement admixture, latex, rubber, and polymer processing.
Nansa HS 85/S has also been used as a teat disinfectant in dairy cattle and used in insecticidal dips for dogs (0.2-0.5 % final dilution).


Nansa HS 85/S has been used with sanitizers for poultry drinking water (30 mg/gal), for washing eggs (150 mg/gal), and on premises and equipment (300 mg/gal).
Nansa HS 85/S can be used as a growth regulator for lily (25% final dilution).


Nansa HS 85/S is used as an absorbant in pesticide and other agricultural chemicals, a foaming and wetting agent in pulp and paper products.
Nansa HS 85/S is used in the foam separation of iron (III) hydroxide flox.
Nansa HS 85/S is used primary Anionic Surfactant.


Nansa HS 85/S is used excellent foaming and detergency properties.
Nansa HS 85/S can be used as an efficient emulsifying agent for polymerizing pressure-sensitive adhesive.
As the main content of high-class detergent and cleaner, Nansa HS 85/S can blench, remove stains and oil and resist static electricity.


Nansa HS 85/S can be used as an antistatic additive with a cleaning function for textile oil.
Nansa HS 85/S can be an efficient antistatic agent for polyester substrate and film base, especially for polyester base cinefilm and filmstrip.
Nansa HS 85/S can be the antistatic agent for polyolefine, polyester, and other polymer materials.


Nansa HS 85/S can be used as the anti-hygroscopic and anticaking additives for powdered chemical products that easily absorb moisture and agglomerate, such as methenamine, carbamide, and ammonium nitrate.
Nansa HS 85/S surfactant can be used as good degreasing for quality leathers.


Nansa HS 85/S is used as textile printing and dyeing auxiliary.
used as silk printing, penetration, and degumming refining auxiliary.
Nansa HS 85/S stipulates as processing auxiliary for food industry.


Nansa HS 85/S is used as an anionic surfactant.
Nansa HS 85/S has excellent foaming power and detergency.
Nansa HS 85/S is used Anionic surfactants.


Because of its low production cost and good performance, Nansa HS 85/S has a wide range of uses.
Nansa HS 85/S is the most used synthetic surfactant for household detergents.
Nansa HS 85/S also produces some inorganic salts such as magnesium and calcium and organic amine salts such as triethanolamine.
Nansa HS 85/S has excellent emulsifying properties and is an important part of mixed emulsifiers for various pesticides.


-Detergent uses of Nansa HS 85/S:
Nansa HS 85/S is a yellow oil, which can form a hexagonal or rhombic strong flake-like crystal.
Nansa HS 85/S has micro toxicity and has been recognized by the international security organization as a safe chemical raw material.


-Washing effect:
Nansa HS 85/S is neutral, sensitive to water hardness, not easy to oxidize, strong foaming power, high detergency, easy to compound with various additives, low cost, mature synthesis process, and application.
Nansa HS 85/S has a wide range of fields and is an excellent anionic surfactant.

Nansa HS 85/S has a significant decontamination effect on particle dirt, protein dirt and oily dirt.
Nansa HS 85/S is particularly effective for washing granular dirt on natural fibers.
The detergency increases with the increase of washing temperature.

The effect of dirt is higher than that of non-ionic surfactants, and the foam is rich.
However, Nansa HS 85/S has two shortcomings.
One is that Nansa HS 85/S has poor resistance to hard water, and its decontamination performance can decrease with the hardness of water.

Therefore, detergents with Nansa HS 85/S as the main active agent must be combined with an appropriate amount of chelating agent.
The second is that Nansa HS 85/S has strong degreasing power, and has a certain irritation to the skin when hand-washed, and the clothes feel poor after washing.
Nansa HS 85/S should be used as a softener to rinse.

In recent years, in order to obtain a better comprehensive cleaning effect, Nansa HS 85/S is often used in combination with aliphatic alcohol polyoxyethylene ether (AEO) and other nonionic surfactants.
The main purpose of Nansa HS 85/S is to prepare various types of liquid, powder, and granular detergents, cleaners and cleaners.


-Emulsifying and dispersing agent uses of Nansa HS 85/S:
Emulsifier is a substance that improves the surface tension between the various constituent phases in the emulsion to form a uniform and stable dispersion system or emulsion.

Emulsifiers are surface-active substances with both hydrophilic and lipophilic groups in the molecule.
They gather on the oil/water interface, which can reduce the interfacial tension and reduce the energy required to form the emulsion, thereby increasing the energy of the emulsion.

As an anionic surfactant, Nansa HS 85/S has good surface activity and strong hydrophilicity, which can effectively reduce the tension of the oil-water interface and achieve emulsification.
Therefore, Nansa HS 85/S is widely used in the preparation of emulsions such as cosmetics, printing and dyeing auxiliaries, and pesticides.


-Antistatic agent uses of Nansa HS 85/S:
Any object has its own static charge, which can be negative or positive.
The accumulation of static charge affects or even harms life or industrial production, and guides and eliminates the accumulated harmful charge so that it is not suitable for production.

The chemicals that cause inconvenience or harm to life are called antistatic agents.
Nansa HS 85/S can make the surface of fabrics, plastics, etc. affinity for water, and the ionic surfactant also has a conductive effect, so it can leak static electricity in time, thereby reducing the danger and inconvenience caused by static electricity


-Industrial uses of Nansa HS 85/S:
These frothers are mixtures of alcohols containing 6–8 carbon atoms.
They were at one time marketed by DuPont and they are tailored frothers for specific ore types.
The bestknown frother from this group is methyl isobutyl carbinol (MIBC) and 2-ethyl hexanol.
Aliphatic alcohol frothers are used as mixtures of different carbon lengths and as a mixture of hydrocarbon oils.


-Antistatic Agent:
All objects have the electrostatic charges.
The charges can be negative charges or positive charges.
The accumulation of static charges affects our life or industrial production.

The chemical used to direct and eliminate harmful electric charges is called the antistatic agent.
Nansa HS 85/S has an electrically conductive function.
Therefore, static electricity can be eliminated in time to reduce the danger and inconvenience caused by static electricity.


-Emulsifier uses of Nansa HS 85/S:
The emulsifier is a kind of substance that improves the surface tension between various components in the emulsion and forms a stable dispersion system or emulsion.

There are hydrophilic groups and lipophilic groups in its molecule.
And they gathered on the oil/water boundary.

They also can reduce the interfacial tension and reduce the energy required to form the emulsion, so as to improve the energy of the emulsion.
As a kind of anionic surfactant, Nansa HS 85/S has good surface activity and strong hydrophilicity.
And Nansa HS 85/S effectively reduces the tension of oil and water surface to emulsification.



ADVANTAGES OF NANSA HS 85/S:
Nansa HS 85/S is used creating high and stable foam; the product is especially recommended for applications where the occurrence of foam is crucial and necessary.
Nansa HS 85/S has in comparison to sulphated alcohols, ABSNa 50 has resistance to hydrolysis in an alkaline environment.
Nansa HS 85/S has excellent detergency, degreasing, wetting, dispersing and emulsifying properties.



AIR AND WATER REACTIONS OF NANSA HS 85/S:
Nansa HS 85/Sis soluble in water.


REACTIVITY PROFILE OF NANSA HS 85/S:
Nansa HS 85/S is incompatible with strong oxidizers.


PURIFICATION METHOS OF NANSA HS 85/S:
Nansa HS 85/S crystallises from propan-2-ol or H2O.



SYNTHETIC METHOD ANALYSIS OF NANSA HS 85/S:
At present, the common production methods of Nansa HS 85/S are as follows.

1. SO3 sulfonation method:
Sulfonation Reaction - Synthesis of Nansa HS 85/S

The reaction is exothermic, and the reaction rate is extremely fast, almost instantaneous.
There are many kinds of side reactions, and the post-treatment steps are many and complex.
Due to the high reactivity of SO3, Nansa HS 85/S is necessary to dilute the liquid with solvent, and dilute the gas with dry air or inert gas.

The advantages of this method are that no water is generated during sulfonation, the amount of sulfur trioxide can be close to the theoretical amount, the reaction is fast, and the waste liquid is small.
However, sulfur trioxide is too active to produce sulfones and other by-products during sulfonation, so Nansa HS 85/S is often diluted with air or solvent.


2. Excessive H2SO4 Sulfonation Method:
Sulfonation Reaction - Synthesis of Nansa HS 85/S
The water generated by the reaction will reduce the concentration of sulfuric acid and the reaction rate, so it is necessary to use a lot of sulfonating agent to make the reaction go smoothly.

Aromatics that are difficult to sulfonate should be sulfonated with oleum.
At this time, the free sulfur trioxide is mainly used, so a lot of sulfonating agent should be used.
Sulfuric acid sulfonation is widely used.

This method has almost no side reaction.
Compared with the first method, the post-treatment is relatively simple, the reaction conditions are mild, the heat release is small, and the conversion rate is high.


3. Sulfonation of Chlorosulfonic Acid
Sulfonation Reaction - Synthesis of Nansa HS 85/S
Chlorosulfonic acid is also a common sulfonating agent, which can be regarded as SO3·HCl complex.

Sulfonation with chlorosulfonic acid can be carried out in greenhouse, the reaction is irreversible, basically according to stoichiometry.
The reaction rate is fast and the yield of the product is high, but chlorosulfonic acid is toxic and hydrogen chloride is produced in the reaction process.

In addition, there are azeotropic dehydration sulfonation method, aromatic primary amine baking sulfonation method and so on.
Here, dodecylbenzene is used as raw material, various factors that need to be considered in the synthesis process are analyzed, the appropriate synthesis scheme is determined, and the feasibility of the scheme is tested by synthesis according to this scheme.



SOURCES OF NANSA HS 85/S:
Nansa HS 85/S is derived from the alkylation of benzene with dodecene (to which benzene attaches itself in any secondary position) in the presence of an alumium chloride catalyst, then sulfonated with sulfuric acid or sulfur trioxide, followed by neutralization with caustic soda (such as sodium hydroxide or sodium carbonate).

Nansa HS 85/S is a straight-chain alkylbenezene sulfonate.
For stright-chained Nansa HS 85/S (LAS), the dodecene may be formed by Ziegler polymerization of ethylene or by cracking wax paraffins to alpha-olefins.
Nansa HS 85/S is a detergent specially tailored for biodegradability.



FORMS OF NANSA HS 85/S:
Nansa HS 85/S may have many isomers.
Nansa HS 85/S can be white to light yellow in color and in the form of flakes, granules, or powder.
Nansa HS 85/S is "non-volatile (vapor is water)".
Nansa HS 85/S can be in commercially available forms containing 62% active matter or 81% purity depending on the manufacturer.



PHYSICAL and CHEMICAL PROPERTIES of NANSA HS 85/S:
Molecular Weight: 348.5 g/mol
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 12
Exact Mass: 348.17351024 g/mol
Monoisotopic Mass: 348.17351024 g/mol
Topological Polar Surface Area: 65.6Ų
Heavy Atom Count: 23
Formal Charge: 0
Complexity: 365
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: 2
Compound Is Canonicalized: Yes
Molecular Weight： 348.47600
Exact Mass： 348.17400

HScode： 3402110000
PSA： 65.58000
XLogP3： 6.13490
Appearance： white or light yellow flakes
Density： 1.02 g/cm3
Melting Point： >300 °C
Melting point: >300 °C
Boiling point: 660.62℃[at 101 325 Pa]
Density: 1.02 g/cm3
vapor pressure: 0 Pa at 25℃
pka: 0.7[at 20 ℃]
form: powder
color: light yellow
Water Solubility: 800mg/L at 25℃
Merck: 14,8612
BRN: 4171051
Stability: Stable.
InChIKey: JHJUUEHSAZXEEO-UHFFFAOYSA-M
LogP: 1.96 at 25℃
FDA 21 CFR: 173.405; 175.300; 175.320; 177.1200; 177.2600; 177.2800; 178.3120

Substances Added to Food (formerly EAFUS): SODIUM DODECYLBENZENESULFONATE
CAS DataBase Reference: 25155-30-0(CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: 554127163Y
EPA Substance Registry System: Sodium dodecylbenzenesulfonate (25155-30-0)
Linear Formula: CH3(CH2)11C6H4SO3Na
MDL Number: MFCD00011508
EC No.: 246-680-4
Beilstein/Reaxys No.: 4171051
Pubchem CID: 23662403
IUPAC Name: sodium; 2-dodecylbenzenesulfonate
SMILES: CCCCCCCCCCCCC1=CC=CC=C1S(=O)(=O)[O-].[Na+]
InchI Identifier: InChI=1S/C18H30O3S.Na/c1-2-3-4-5-6-7-8-9-10-11-14-17-15-12-13-16-18(17)22(19,20)21;/h12-13,15-16H,2-11,14H2,1H3,(H,19,20,21);/q;+1/p-1
InchI Key: HFQQZARZPUDIFP-UHFFFAOYSA-M
Physical state: powder
Color: light yellow
Odor: No data available
Melting point/freezing point:
Melting point: > 300 °C
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: 7 - 10,5 at 25 °C- OCSPP 830.7000
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 0,8 g/l at 25 °C - soluble
Partition coefficient: n-octanol/water: log Pow: 1,96 at 25 °C
Vapor pressure: No data available
Density: 1 g/cm3 at 20 °C
Relative density: 1 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information:
Surface tension: 29,3 - 31,8 mN/m at 120g/l at 25 °C



FIRST AID MEASURES of NANSA HS 85/S:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of NANSA HS 85/S:
-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 NANSA HS 85/S:
-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 NANSA HS 85/S:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*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 NANSA HS 85/S:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of NANSA HS 85/S:
-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



SYNONYMS:
Benzenesulfonic acid,dodecyl-,sodium salt (1:1)
Benzenesulfonic acid,dodecyl-,sodium salt
Sodium laurylbenzenesulfonate
Stepan DS 60
Ultrawet 1T
Marlon A 350
Sodium dodecylphenylsulfonate
Sulframin 85
Marlon A
Dodecylbenzenesulfonic acid sodium salt
Maranil
Marlon A 375
Nacconol 35SL
Siponate DS 10
Trepolate F 40
Conoco C 550
KB (surfactant)
Nansa SL
Santomerse Me
Merpisap AP 90P
Nansa SS
Trepolate F 95
Nansa HS 80
Deterlon
Ultrawet 99LS
Sulfuril 50
F 90
Elfan WA Powder
Sandet 60
Steinaryl NKS 50
Sinnozon
Nansa HS 85S
C 550
KB
HS 85S
Nansa HF 80
Arylan SBC
Marlon 375A
X 2073
Conco AAS 35H
Neopelex 05
Richonate 40B
DS 60
Pelopon A
Sulframin 1240
Richonate 1850
35SL
Calsoft L 40
Calsoft F 90
SDBS
Alkanate DC
Sulfaril Paste
Steinaryl NKS 100
Siponate DS 4
Siponate LDS 10
Nestapone
Nansa 1260
Marlon 375
Neopelex F 60
Abeson NAM;Emulin B 22
Neopelex 6
Bio-Soft D 40
Neogen SC
Nissan Newrex R
Conco AAS 35
Reworyl NKS 50
Elfan WA 35
Neopelex 25
Elfan WA 50
MB-VR
Marlon A 396
Neopelex F 25
Witconate 1238
Sulframin 40
Nacconol 40F
Nansa HS 80S
Conco AAS 45S
Newrex R
A 1-1575
Nansa 1106
Maranil A 55
Neopelex 6E
Liponox LE 110
Nissan Newrex H
Vista C 550
Witconate 1250
Conco AAS 40S
Bio-Soft D 35X
Stepantan DS 40
Phenyl Sulfonate HSR
Deterlon A
Polystep A 15
Nansa HS 80SA
Bio-Soft LAS 40S
Witconate 60B
Nissan Newrex F
Newrex Powder F
F 90 (sulfonic acid)
Nansa SSA 055
Newrex T
1323-13-3
11114-21-9
12068-21-2
12627-25-7
12676-70-9
18618-53-6
19327-14-1
28675-02-7
37334-89-7
39316-39-7
39386-98-6
39405-16-8
52624-37-0
56590-39-7
57762-50-2
58517-33-2
60328-33-8
63530-22-3
68445-25-0
71244-85-4
76483-01-7
82028-94-2
82785-43-1
83203-33-2
83652-87-3
83652-88-4
83652-89-5
88495-86-7
90452-02-1
94187-92-5
122390-78-7
128452-17-5
138362-06-8
142986-60-5
147035-77-6
167163-39-5
170006-86-7
177645-67-9
178900-97-5
189201-38-5
254117-47-0
295348-93-5
312629-70-2
352212-18-1
AA-9
AA-10
ABESON NAM
ARYLAN SBC
BENZENESULFONIC ACID
DODECYL-, SODIUM SALT
BIO-SOFT D-40
BIO-SOFT D-35X
C 550
CALSOFT F-90
CALSOFT L-40
CONCO AAS-35
CONCO AAS-40
CONCO AAS-50
CONCO AAS-35H
CONCO AAS-40S
CONCO AAS-45S
CONOCO C 550
CONOCO C-50
CONOCO C-60
CONOCO SD 40
CONOCO SD C-40
DETERGENT HD-90
DETERLON
DODECYLBENZENESULFONIC ACID SODIUM SALT
DODECYLBENZENESULPHONATE, SODIUM SALT
DODECYL BENZENE SODIUM SULFONATE
DODECYLBENZENSULFONAN SODNY (Czech)
p-DODECYLBENZENSULFONAN SODNY (Czech)
ELFAN WA POWDER
F 90
HS 85S
KB
KB (SURFACTANT)
MARANIL
MARLON 375
MARLON A
MARLON A 350
MARLON A 375
MERCOL 25
MERCOL 30
MERPISAP AP 90P
NACCANOL NR
NACCANOL SW
NACCANOL 35SL
NANSA HS 80
NANSA HS 85S
NANSA SL
NANSA SS
NEOPELEX 05
PELOPON A
PILOT HD-90
PILOT SF-40
PILOT SF-40B
RICHONATE 1850
RICHONATE 45B
SANDET 60
SANTOMERSE 3
SANTOMERSE ME
SANTOMERSE NO. 1
SANTOMERSE NO. 85
SDBS
SINNOZON
SIPONATE DS 10
SODIUM DODECYLBENZENESULFONATE
SODIUM DODECYLBENZENESULFONATE, dry
SODIUM DODECYLBENZENESULPHONATE
SODIUM DODECYLPHENYLSULFONATE
SODIUM LAURYLBENZENESULFONATE
SOLAR 40
STEINARYL NKS 50
STEINARYL NKS 100
STEPAN DS 60
STEPANTAN DS 40
SULFAPOL
SULFAPOLU (Polish)
SULFARIL PASTE
SULFRAMIN 85
SULFRAMIN 40 FLAKES
SULFRAMIN 40 GRANULAR
SULFRAMIN 40RA
SULFRAMIN 85
SULFRAMIN 90 FLAKES
SULFRAMIN 1238 SLURRY
SULFRAMIN 1240
SULFRAMIN 1250 SLURRY
SULFURIL
SULFURIL 50
TREPOLATE F 40
TREPOLATE F 95
ULTRAWET 1T
ULTRAWET 60K
ULTRAWET 99LS
ULTRAWET K
ULTRAWET KX
ULTRAWET SK
VISTA C 550
WITCONATE 60 B
WITCONATE 1248
WITCONATE 1250
X 2073
BENZENE SULFONIC ACID, DODECYL-, SODIUM SALT
BIO-SOFT
BIO-SOFT D-60
BIO-SOFT D-62
CALSOFT
CALSOFT L-60
CONCO AAS-65
CONCO AAS-90
CONCO C-50
CONCO C-60
CONCO SD 40
DODECYLBENZENE SODIUM SULFONATE
DODECYLBENZENESULFONATE, SODIUM SALT
NACCONOL 35SL
NACCONOL 40F
NACCONOL 90F
NECCANOL SW
PILOT SF-40FG
PILOT SF-60
PILOT SF-96
PILOT SP-60
RICHONATE
RICHONATE 60B
SODIUM DODECYLBENZENE SULFONATE
SODIUM DODECYLBENZENESULFONATE (BRANCHED CHAIN)
SODIUM DODECYLBENZENESULPHONATE (BRANCHED CHAIN)
SODIUM LAURLYBENZENESULFONATE
SODIUM SALT DODECYLBENZENESULFONIC ACID
SOLAR 90
SULFONATE DODECYLBENZENE
SULFRAMIN
SULFRAMIN 40 CRANULAR
Sodium o-dodecylbenzenesulfonate
15163-46-9
Sodium dodecylbenzenesulphonate
2-Dodecylbenzenesulfonic acid, sodium salt
Dodecyl benzenesulfonic acid, sodium salt
SDBS
sodium 2-dodecylbenzenesulfonate
sodium dodecyl benzene sulfonate
sodium;2-dodecylbenzenesulfonate
Benzenesulfonic acid, dodecyl-, sodium salt
Sodium o-dodecylbenzenesulphonate
12627-25-7
Benzenesulfonic acid, 2-dodecyl-, sodium salt
Benzenesulfonic acid, 2-dodecyl-, sodium salt (1:1)
2855754K9T
37334-89-7
Abeson nam
Santomerse 3
Sulframin 85
sodiumdodecylbenzenesulphonate
Sulfapolu
Sulfuril
Sulfaril paste
Ultrawet K
Ultrawet KX
Ultrawet SK
Richonate 45B
Sulframin 40RA
UNII-2855754K9T
Ultrawet 60K
Detergent HD-90
Santomerse No. 1
Stepantan DS 40
Trepolate F 40
Witconate 60 B
EINECS 239-219-3
Conco aas-35
Conco aas-35H
Conco aas-40
Conco aas-40S
Conco aas-45S
Conco aas-50
Mercol 25
Mercol 30
Richonate 1850
Sandet 60
Steinaryl NKS 50
Witconate 1238
Witconate 1250
Calsoft F-90
Calsoft L-40
Sulframin 40 flakes
Sulframin 90 flakes
Santomerse No. 85
Stepan DS 60
Caswell No. 765
Pilot SF-40B
Steinaryl NKS 100
Bio-Soft D-35X
Sulframin 40 granular
Bio-Soft D-40
Vista C 550
Sulframin 1238 slurry
Sulframin 1250 slurry
Dodecylbenzensulfonan sodny
Sodium dodecylphenylsulfonate
p-Dodecylbenzensulfonan sodny
SCHEMBL24015
Sodium lauryl benzene sulfonate
AA-9
HSDB 740
Dodecyl benzene sodium sulfonate
DTXSID0041642
Sodium dodecylbenzenesulfonic acid
HFQQZARZPUDIFP-UHFFFAOYSA-M
AA-10
Dodecylbenzenesulphonate, sodium salt
EINECS 246-680-4
Sodium dodecylbenzenesulphonate, pure
UNII-554127163Y
AKOS015912936
EPA Pesticide Chemical Code 079010
Sol sodowa kwasu laurylobenzenosulfonowego
EC 246-680-4
X 2073
Benzenesulfonic acid, dodecyl-, sodium salt (1:1)
BENZENESULFONIC ACID, O-DODECYL-, SODIUM SALT
P-1',1',4',4'-Tetramethyloktylbenzensulfonan sodny
Q27254266
554127163Y
11114-21-9
12068-21-2
1323-13-3
28675-02-7
39316-39-7
39386-98-6
39405-16-8
52624-37-0
58517-33-2
60328-33-8
68445-25-0
71244-85-4
82028-94-2
82785-43-1
sdbs
SODIUM DODECYLBENZENESULFONATE
Sodium dodecyL
DDBS
LAS-C12
DODECYLBENZENE SODIUM SULFONATE
SODIUM ALKYLBENZENESULFONATE
Sodium dodecyl-benzenesuffonate
DODECYLBENZENESULFONIC ACID SODIUM SALT
aa-9
Dodecylbenzene sodium sulfonate
Dodecylbenzenesulfonic acid sodium salt
linear alkylbenzene sulfonate
LAS
2-Dodecylbenzenesulfonic acid, sodium salt
sodium dodecyl sulfonate
sodium dodecylsulphonate
sodium 2-dodecylbenzenesulfonate
sodium 4-dodecylbenzenesulfonate
Sodium P-dodecylbenzenesulfonate
Benzenesulfonic acid, 2-dodecyl-, sodium salt
15163-46-9
11114-21-9
2211-98-5
1322-98-1

DESCRIPTION:

NANSA HS 90 / NPF is a sodium alkyl benzene sulfonate powder based on a predominately straight chain alkylate.
NANSA HS 90 / NPF does not contain phosphate or magnesium.
NANSA HS 90 / NPF is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.

The physical form allows direct incorporation into powders, compressed tablets and blocks.

SAFETY INFORMATION ABOUT NANSA HS 90/NPF:
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

Nansa HS 90/NPF is a sodium alkyl benzene sulfonate powder.
Nansa HS 90/NPF is predominantly composed of straight-chain alkylate molecules.
Nansa HS 90/NPF does not contain phosphate or magnesium in its composition.



APPLICATIONS


Nansa HS 90/NPF is a versatile sodium alkyl benzene sulfonate powder used in a variety of applications.
Nansa HS 90/NPF is a key ingredient in the formulation of laundry detergents, contributing to their cleaning effectiveness.

Nansa HS 90/NPF enhances the removal of dirt, stains, and grime from fabrics in both home and commercial settings.
Nansa HS 90/NPF is found in powdered laundry detergents, ensuring efficient stain removal.

Nansa HS 90/NPF is employed in liquid laundry detergents to boost their detergency and emulsification properties.
Nansa HS 90/NPF plays a role in the formulation of heavy-duty stain removers and pre-treatment products.

Nansa HS 90/NPF contributes to the effectiveness of industrial laundry detergents used in commercial laundries and hospitality industries.
Nansa HS 90/NPF is used in the creation of fabric softeners, leaving fabrics soft and fresh after washing.
Nansa HS 90/NPF can be found in laundry pods and tablets, providing a convenient and pre-measured dose of detergent.

Nansa HS 90/NPF is used in industrial and institutional cleaning products for surface cleaning and degreasing.
Surface cleaners benefit from its ability to remove dirt and grease from a variety of surfaces.

Nansa HS 90/NPF contributes to the formulation of kitchen and bathroom cleaners, ensuring thorough cleaning and disinfection.
Nansa HS 90/NPF enhances the cleaning performance of floor cleaners for homes and commercial spaces.
Nansa HS 90/NPF is employed in the manufacturing of specialty cleaning products for automotive interiors and exteriors.
Nansa HS 90/NPF is found in glass and window cleaning solutions, leaving surfaces streak-free and clear.

Nansa HS 90/NPF aids in the creation of multi-purpose household cleaners for everyday use.
Nansa HS 90/NPF is used in industrial degreasers for machinery and equipment maintenance.

Nansa HS 90/NPF contributes to the production of rust and scale removers for various applications.
Nansa HS 90/NPF plays a role in the formulation of specialty cleaning wipes for convenient and effective cleaning.

Nansa HS 90/NPF can be found in industrial and commercial kitchen cleaning solutions.
Nansa HS 90/NPF enhances the cleaning power of janitorial cleaning products used in office and institutional settings.

Nansa HS 90/NPF is employed in the creation of specialty cleaning products for healthcare facilities.
Nansa HS 90/NPF contributes to the formulation of environmentally friendly and eco-conscious cleaning solutions.
Nansa HS 90/NPF is a versatile ingredient in the production of cleaning products used across industries, from automotive to hospitality.
Its cleaning effectiveness and emulsification properties make it an essential component in delivering high-quality and efficient cleaning solutions for various applications.

Nansa HS 90/NPF is utilized in the formulation of carpet and upholstery cleaners for homes and businesses.
Nansa HS 90/NPF aids in the creation of rug and carpet spot removers, effectively targeting stains and spills.

Nansa HS 90/NPF is found in dry carpet powders used for odor and stain removal.
Nansa HS 90/NPF plays a role in the production of industrial and institutional floor stripping agents.
Nansa HS 90/NPF enhances the cleaning power of automotive interior cleaners and upholstery shampoos.

Nansa HS 90/NPF is used in the manufacturing of aircraft interior cleaning solutions.
Nansa HS 90/NPF can be found in specialty cleaning products designed for electronic devices and screens.
Nansa HS 90/NPF aids in the formulation of bathroom and toilet bowl cleaners for thorough sanitation.

Nansa HS 90/NPF is used in the creation of rust and scale removers for various applications, including plumbing maintenance.
Nansa HS 90/NPF contributes to the effectiveness of degreasers used in engine and machinery cleaning.
Nansa HS 90/NPF is utilized in the production of surface sanitizers and disinfectants.

Nansa HS 90/NPF plays a role in creating cleaning solutions for restaurant and food service equipment.
Nansa HS 90/NPF is used in boat and marine cleaning products, including hull cleaners and deck washes.
Nansa HS 90/NPF is employed in pool and spa cleaning solutions, maintaining water clarity and hygiene.

Nansa HS 90/NPF aids in the formulation of janitorial cleaning products used in commercial and institutional settings.
Nansa HS 90/NPF is utilized in the creation of agricultural and farm cleaning solutions for equipment and facilities.

Nansa HS 90/NPF contributes to the cleaning and maintenance of industrial and automotive parts.
Nansa HS 90/NPF enhances the cleaning performance of concrete and driveway cleaners.

Nansa HS 90/NPF plays a role in creating pressure washing solutions for outdoor surfaces, including siding and decks.
Nansa HS 90/NPF is employed in the formulation of concrete and masonry cleaners for construction projects.
Nansa HS 90/NPF contributes to the effectiveness of rust preventatives used in metalworking and manufacturing.

Nansa HS 90/NPF aids in the production of degreasing agents for various industries, including automotive and aerospace.
Nansa HS 90/NPF is used in the formulation of adhesive and sealant removers for industrial applications.

Nansa HS 90/NPF plays a role in the creation of specialty cleaning products for the removal of graffiti and paint.
Nansa HS 90/NPF's versatility extends to a wide range of cleaning and maintenance applications, making it a valuable component in delivering effective and efficient cleaning solutions for residential, commercial, and industrial use.



DESCRIPTION


Nansa HS 90/NPF is a sodium alkyl benzene sulfonate powder.
Nansa HS 90/NPF is predominantly composed of straight-chain alkylate molecules.
Nansa HS 90/NPF does not contain phosphate or magnesium in its composition.

Nansa HS 90/NPF is classified as a high-active anionic surfactant.
Its primary functions include wetting, detergency, and emulsification.

Nansa HS 90/NPF is a versatile ingredient used in various cleaning and detergent formulations.
Nansa HS 90/NPF's wetting properties ensure thorough and effective surface coverage.

Nansa HS 90/NPF is particularly known for its strong detergency, making it highly effective at removing dirt, stains, and grease.
Its emulsifying capabilities allow it to effectively mix oils with water-based solutions.
Nansa HS 90/NPF finds applications in a wide range of products, including laundry detergents.

Nansa HS 90/NPF is commonly used in the formulation of laundry detergents to improve cleaning performance.
Surface cleaners benefit from the product's ability to provide effective cleaning and stain removal.
Nansa HS 90/NPF is used in the production of hygienic blocks for various applications.

The physical form of the chemical, as a powder, allows for direct incorporation into product formulations.
Its compatibility with various product formats, including powders and compressed tablets, makes it versatile for manufacturers.

Notably, Nansa HS 90/NPF is free from phosphate, making it suitable for formulations where phosphate is restricted or undesired.
Similarly, Nansa HS 90/NPF does not contain magnesium, which can be an advantage in certain applications.
Nansa HS 90/NPF contributes to the creation of high-quality cleaning products.
Its cleaning power is essential for effectively removing tough stains and residues.

Manufacturers appreciate its ease of incorporation into their cleaning formulations.

Nansa HS 90/NPF is known for enhancing the overall cleaning experience for consumers.
Its anionic nature allows it to work effectively in water-based solutions.

Nansa HS 90/NPF can be used in both household and industrial cleaning products.
Its versatility and effectiveness make it a valuable ingredient in the detergent and cleaning industry.
When used according to recommended guidelines, Nansa HS 90/NPF contributes to the creation of efficient, high-performing cleaning solutions.



PROPERTIES


Chemical Name: Nansa HS 90/NPF
Chemical Composition: Sodium alkyl benzene sulfonate powder, predominantly straight-chain alkylate molecules, phosphate-free, and magnesium-free.



FIRST AID


Inhalation:

If inhaled, immediately move the affected person to an area with fresh air.
Allow the person to rest in a comfortable position and keep them warm.
If breathing difficulties persist or if there are signs of respiratory distress, seek immediate medical attention.
If breathing has stopped, perform artificial respiration if trained to do so.


Skin Contact:

In case of skin contact, promptly remove contaminated clothing.
Wash the affected skin area gently but thoroughly with plenty of water and mild soap.
If skin irritation, redness, or rash develops, seek medical attention.
If the chemical is in powder form, carefully brush off excess powder before washing with water.


Eye Contact:

If the chemical comes into contact with the eyes, immediately rinse the affected eye(s) gently with lukewarm, running water for at least 15 minutes.
Hold the eyelids open to ensure thorough rinsing.
Seek immediate medical attention if eye irritation or redness persists or if there is any discomfort.


Ingestion:

If Nansa HS 90/NPF is ingested, do not induce vomiting unless directed to do so by medical professionals.
Rinse out the mouth with water if the person is conscious and able to do so.
Seek immediate medical attention or contact a poison control center.
Provide the medical personnel with detailed information about the ingested substance.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate personal protective equipment (PPE) when handling Nansa HS 90/NPF.
This may include safety goggles, gloves, protective clothing, and, if necessary, respiratory protection.

Ventilation:
Work in a well-ventilated area to minimize inhalation exposure.
Use local exhaust ventilation or general dilution ventilation if needed.

Avoid Contact:
Avoid skin and eye contact with the chemical.
Use caution to prevent ingestion or inhalation.
Do not eat, drink, or smoke while handling the product.

Handling Precautions:
Handle with care to avoid spills and splashes.
Follow safe handling procedures, and minimize the generation of dust or aerosols when working with powdered forms.

Storage Containers:
Ensure that containers used for transferring or storing the chemical are clean, dry, and compatible with the product.
Use containers made of materials resistant to chemical reactions.

Labeling:
Clearly label all containers with the product name, hazard information, and appropriate safety warnings.

Storage Temperature:
Store in a cool, dry place away from direct sunlight and heat sources.
Follow any specific temperature storage recommendations provided by the manufacturer.

Storage Area:
Store Nansa HS 90/NPF in a dedicated storage area or cabinet away from incompatible materials, such as strong acids, strong bases, and oxidizing agents.

Segregation:
Keep the chemical separated from food items, beverages, and personal items to prevent contamination.


Storage:

Temperature:
Store the chemical within the recommended temperature range as specified in the SDS.
Avoid extreme temperature fluctuations.

Humidity:
Maintain proper humidity control to prevent clumping or caking in powdered forms.

Ventilation:
Ensure that the storage area is well-ventilated to prevent the buildup of fumes or vapors.

Sealing:
Keep containers tightly sealed when not in use to prevent moisture absorption and contamination.

Inventory Management:
Implement a first-in, first-out (FIFO) inventory management system to use older stock before newer stock.

Secondary Containment:
Use secondary containment measures such as spill trays or bunds to contain any potential leaks or spills.

Emergency Response:
Have spill control equipment, absorbents, and spill response materials readily available in the storage area.

Accessibility:
Ensure that the storage area is easily accessible for inspections and emergency response.

DESCRIPTION:

NANSA HS 90 / S is a high active sodium alkyl benzene sulphonate based on a predominately straight chain alkylate.
NANSA HS 90 / S is a high active anionic surfactant particularly suited to provide wetting, detergency and emulsification in a wide range of applications, including laundry detergents, surface cleaners and hygienic blocks.
The physical form allows direct incorporation into powders, compressed tablets and blocks.



SAFETY INFORMATION ABOUT NANSA HS 90/S:
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

Nansa HS 90/S is a versatile sodium alkyl benzene sulphonate surfactant.
Nansa HS 90/S belongs to the category of anionic surfactants, known for their effective cleaning properties.
Nansa HS 90/S is based on a predominantly straight chain alkylate, contributing to its stability and effectiveness.

CAS Number: 68411-30-3
EC Number: 90194-45-9



APPLICATIONS


Nansa HS 90/S has many different applications:

Laundry Detergents:
Nansa HS 90/S is a key ingredient in laundry detergents, ensuring the effective removal of stains and soil from clothing and fabrics.

Surface Cleaners:
Nansa HS 90/S is commonly used in surface cleaning products for homes, offices, and industrial settings, making surfaces spotless and free of contaminants.

Hygienic Blocks:
Nansa HS 90/S contributes to the formulation of hygienic blocks used for cleaning and disinfection in bathrooms and restrooms.

Kitchen Cleaners:
Nansa HS 90/S is found in kitchen cleaning products, helping to remove grease, grime, and food residues from countertops, appliances, and cookware.

Bathroom Cleaners:
Nansa HS 90/S aids in bathroom cleaning solutions, ensuring the cleanliness and hygiene of toilets, sinks, and showers.

Floor Cleaners:
Nansa HS 90/S is used in floor cleaners, effectively removing dirt and stains from various types of flooring.

Glass Cleaners:
Nansa HS 90/S enhances the performance of glass cleaners, leaving glass surfaces streak-free and crystal clear.

Carpet Cleaners:
Nansa HS 90/S is employed in carpet cleaning formulations, assisting in the removal of tough stains and odors.

Automotive Cleaners:
In the automotive industry, it is used in cleaning products for vehicles, including exterior and interior surfaces.

Industrial Degreasers:
Nansa HS 90/S plays a crucial role in industrial degreasers, effectively removing grease and oil from machinery and equipment.

Metal Cleaners:
Nansa HS 90/S contributes to metal cleaning solutions, ensuring the removal of rust, scale, and contaminants from metal surfaces.

Agricultural Equipment:
Nansa HS 90/S is used in cleaning products for agricultural equipment, promoting longevity and efficiency.

Printing Industry:
Nansa HS 90/S is incorporated into cleaning solutions for the printing industry, helping to maintain the quality of printing presses and equipment.

Paint Strippers:
In paint stripper formulations, it assists in the removal of paint and coatings from various surfaces.

Janitorial Supplies:
Nansa HS 90/S is a staple in janitorial cleaning supplies used in commercial and institutional cleaning.

Swimming Pool Cleaners:
Nansa HS 90/S can be found in pool cleaning products, ensuring pool water remains clean and free of contaminants.

Furniture Cleaners:
Nansa HS 90/S enhances the performance of furniture cleaners, keeping upholstery and surfaces looking fresh and clean.

Restaurant and Food Service:
Nansa HS 90/S contributes to cleaning solutions used in restaurants and food service establishments, ensuring hygiene and food safety.

Healthcare Facilities:
Nansa HS 90/S is used in cleaning solutions for healthcare settings, including hospitals and clinics, to maintain cleanliness and disinfection.

Public Transportation:
Nansa HS 90/S is employed in cleaning solutions for buses, trains, and public transportation vehicles to ensure passenger safety and comfort.

Electronics Manufacturing:
In electronics manufacturing, the chemical can be part of cleaning solutions for printed circuit boards (PCBs) and components.

Facility Maintenance:
Nansa HS 90/S aids in the maintenance and cleanliness of various facilities, from offices to factories.

Warehouse Cleaning:
Nansa HS 90/S ensures the cleanliness of warehouses and storage areas, facilitating a safe and organized environment.

Garden Equipment Maintenance:
In the gardening industry, it is employed in cleaning solutions for maintaining garden equipment.

Sports Equipment Cleaners:
Nansa HS 90/S aids in cleaning and sanitizing sports equipment, ensuring player safety and hygiene.

Aerospace Industry:
In the aerospace sector, Nansa HS 90/S is used in cleaning and degreasing aircraft components and surfaces to maintain safety and performance.

Marine Industry:
Nansa HS 90/S is employed in marine cleaning products to remove salt deposits, algae, and contaminants from boat surfaces and equipment.

Oil and Gas:
Nansa HS 90/S aids in cleaning and maintaining equipment in the oil and gas industry, where cleanliness is critical for safety and efficiency.

Power Plants:
Nansa HS 90/S is used in power plant maintenance to clean and degrease machinery and components, ensuring reliable operation.

Electronics Cleaning:
In the electronics industry, it helps remove flux residues and contaminants from circuit boards and electronic components.

HVAC Systems:
Nansa HS 90/S is used in cleaning solutions for HVAC (heating, ventilation, and air conditioning) systems to improve indoor air quality.

Construction Equipment:
Nansa HS 90/S contributes to cleaning and maintaining construction machinery and equipment, extending their lifespan.

Mining Industry:
Nansa HS 90/S aids in the cleaning of mining equipment and facilities, promoting safety and operational efficiency.

Automotive Industry:
Beyond vehicle cleaning, it is used in automotive manufacturing for parts cleaning and paint preparation.

Textile Industry:
Nansa HS 90/S is found in textile cleaning formulations, assisting in fabric dyeing and finishing processes.

Chemical Industry:
Nansa HS 90/S is used for cleaning and maintaining equipment in chemical manufacturing plants.

Plastics Industry:
In plastics processing, it helps clean and prepare molds and machinery for production.

Water Treatment:
Nansa HS 90/S can be part of water treatment formulations to remove impurities and contaminants from water sources.

Food Processing:
Nansa HS 90/S is used in cleaning solutions for food processing equipment to maintain hygiene and safety standards.

Pulp and Paper:
Nansa HS 90/S contributes to cleaning and maintaining machinery in the pulp and paper industry, ensuring smooth production.

Pharmaceutical Industry:
Nansa HS 90/S aids in cleaning and sanitizing pharmaceutical manufacturing equipment to meet stringent quality standards.

Cosmetic Industry:
In cosmetics manufacturing, it is used in cleaning and preparing containers and equipment for product filling.

Research Laboratories:
Nansa HS 90/S plays a role in maintaining cleanliness in research laboratories, including glassware and equipment cleaning.

Waste Management:
Nansa HS 90/S is used in cleaning solutions for waste management equipment and facilities.

Firefighting Equipment:
Nansa HS 90/S assists in cleaning and maintaining firefighting gear and equipment.

Art Conservation:
In art restoration and conservation, it helps clean and restore artworks and artifacts.

Photography:
Nansa HS 90/S is used in photography laboratories for cleaning and processing photographic materials.

Educational Institutions:
Nansa HS 90/S contributes to maintaining cleanliness in educational facilities, including classrooms and laboratories.

Hospitals and Clinics:
Nansa HS 90/S is used in healthcare settings for cleaning and disinfecting medical equipment.

Hotels and Hospitality:
In the hospitality industry, it is employed in cleaning solutions for guest rooms, public areas, and laundry services, ensuring a pleasant stay for guests.



DESCRIPTION


Nansa HS 90/S is a versatile sodium alkyl benzene sulphonate surfactant.
Nansa HS 90/S belongs to the category of anionic surfactants, known for their effective cleaning properties.
Nansa HS 90/S is based on a predominantly straight chain alkylate, contributing to its stability and effectiveness.

Nansa HS 90/S is recognized for its high activity, making it potent in various applications.
As a surfactant, Nansa HS 90/S reduces the surface tension of liquids, allowing them to interact more effectively with other substances.

Nansa HS 90/S acts as an efficient wetting agent, ensuring that liquids can easily spread and penetrate surfaces.
Nansa HS 90/S exhibits strong detergency, making it highly effective in removing dirt, grease, and stains.

Nansa HS 90/S aids in emulsification, facilitating the dispersion of one liquid into another, which is crucial in various formulations.
Its detergency and wetting properties contribute to its excellent cleaning performance.
Nansa HS 90/S is a valuable ingredient in laundry detergents, ensuring thorough cleaning and stain removal from fabrics.

Nansa HS 90/S enhances the cleaning power of surface cleaners, making it easier to remove dirt and grime from various surfaces.
Nansa HS 90/S is commonly used in the formulation of hygienic blocks, promoting cleanliness and disinfection.

The physical form of this surfactant allows for direct incorporation into powdered cleaning products.
Nansa HS 90/S can be utilized in the production of compressed cleaning tablets, offering convenience and ease of use.
Nansa HS 90/S plays a crucial role in creating solid cleaning blocks designed for a range of applications.

Nansa HS 90/S is identified by the CAS number 68411-30-3, a unique identifier for chemical compounds.
Nansa HS 90/S is associated with the EC number 90194-45-9, aiding in its classification and reference in regulatory documents.
Nansa HS 90/S is frequently used in household cleaning products, ensuring cleanliness and hygiene in homes.
Nansa HS 90/S finds applications in industrial cleaning and maintenance, effectively removing residues and contaminants.

Manufacturers often incorporate Nansa HS 90/S into formulations designed with environmental sustainability in mind.
Nansa HS 90/S may possess biodegradable properties, which can be advantageous for environmentally friendly products.

Its presence in cleaning formulations contributes to user-friendly products that deliver efficient results.
Nansa HS 90/S maintains stability in various conditions, ensuring consistent performance over time.
When handled and used according to guidelines, it meets safety standards for formulation and usage.
Its versatility makes it a valuable component in a wide range of cleaning and hygiene products, contributing to their efficacy.



PROPERTIES


Chemical Composition: Nansa HS 90/S is composed of sodium alkyl benzene sulphonate, based primarily on a straight-chain alkylate structure.
Anionic Surfactant: It falls into the category of anionic surfactants, known for their ability to lower the surface tension of liquids.
High Activity: Nansa HS 90/S is recognized for its high activity, indicating its potency and effectiveness in various applications.
Surface Tension Reduction: As a surfactant, it reduces the surface tension of liquids, promoting their interaction with other substances.
Wetting Agent: This chemical acts as an efficient wetting agent, allowing liquids to spread easily and penetrate surfaces.
Detergency Properties: Nansa HS 90/S offers strong detergency, making it highly effective in removing dirt, grease, and stains.
Emulsification Capabilities: It aids in emulsification, facilitating the dispersion of one liquid into another, a vital process in many formulations.
Cleaning Performance: Nansa HS 90/S's detergency and wetting properties contribute to its excellent cleaning performance.
pH Range: Nansa HS 90/S is often compatible with a wide pH range, providing versatility in formulation.
Stability: The chemical maintains stability under different conditions, ensuring consistent performance.



FIRST AID


Inhalation:

If inhaled, remove the affected person to a well-ventilated area with fresh air.
If the person is experiencing difficulty breathing, seek immediate medical attention.
In case of severe inhalation exposure, administer artificial respiration if the person has stopped breathing but has a pulse.


Skin Contact:

In case of skin contact, immediately remove contaminated clothing and footwear.
Wash the affected skin thoroughly with soap and water for at least 15 minutes, ensuring that all traces of the chemical are removed.
Seek medical attention if skin irritation, redness, or other adverse reactions persist.


Eye Contact:

If the chemical comes into contact with the eyes, immediately rinse the affected eye(s) with gently flowing lukewarm water for at least 15 minutes.
Keep the affected eye open during rinsing to ensure thorough flushing.
Seek immediate medical attention or consult with an eye specialist if irritation, pain, or visual disturbances continue.


Ingestion:

If swallowed, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water if the chemical is accidentally ingested.
Seek immediate medical attention or contact a poison control center for guidance.


General First Aid:

If a person exhibits signs of chemical exposure, such as dizziness, nausea, or respiratory distress, move them to a safe area with fresh air.
Keep the affected person calm and reassure them while awaiting medical assistance.
Provide first aid based on the specific symptoms and conditions observed.



HANDLING AND STORAGE


Handling:

Protective Equipment:
When handling Nansa HS 90/S, wear appropriate personal protective equipment (PPE), including safety goggles or a face shield, gloves, and protective clothing, to minimize the risk of skin and eye contact.

Ventilation:
Use the product in well-ventilated areas to prevent the buildup of vapors or fumes.
Ensure proper ventilation systems are in place, such as local exhaust ventilation, if necessary.

Avoid Inhalation:
Avoid inhaling vapors or mists.
If airborne concentrations exceed recommended exposure limits, use respiratory protection in accordance with applicable regulations.

Prevent Contamination:
Prevent contamination of the product and maintain cleanliness in the work area.
Use clean equipment and tools when handling and transferring the chemical.

Avoid Mixing:
Avoid mixing Nansa HS 90/S with incompatible substances or chemicals unless directed by specific formulations.
Consult the safety data sheet (SDS) for compatibility information.

Spill Response:
In the event of a spill, follow appropriate spill control procedures outlined in the SDS.
This may include using absorbent materials to contain and clean up spills.
Report larger spills to the relevant authorities.

Hygiene: After handling the chemical, wash hands and any exposed skin thoroughly with soap and water to remove any residues.
Do not eat, drink, or smoke while handling the product.


Storage:

Storage Conditions:
Store Nansa HS 90/S in a cool, dry, well-ventilated area away from direct sunlight and sources of heat or ignition.

Temperature Control:
Maintain storage temperatures within the recommended range specified in the product's SDS or on the product label.

Container Integrity:
Ensure that containers used for storage are tightly sealed and in good condition to prevent leaks or spills.

Incompatible Materials:
Store the chemical away from incompatible materials, such as strong acids, strong bases, and oxidizing agents, to prevent reactions or contamination.

Labeling:
Clearly label containers with the product name, hazard information, and handling precautions.
Keep all labeling information visible and legible.

Accessibility:
Store the chemical in an area that is easily accessible and away from unauthorized personnel, especially children and pets.

Separation:
If multiple chemicals are stored in the same area, separate them according to compatibility guidelines to prevent cross-contamination or hazardous reactions.

Fire Safety:
Take precautions to prevent ignition sources in storage areas, and ensure compliance with local fire safety regulations.

Security:
Implement security measures as necessary to protect the chemical from theft, vandalism, or unauthorized access.



SYNONYMS


Sodium alkyl benzene sulphonate.
High active sodium alkyl benzene sulphonate.
Sodium alkylbenzenesulfonate.
Sodium dodecylbenzene sulfonate.
Sodium linear alkylbenzene sulfonate.
Straight chain alkyl benzene sulphonate.
Sodium LAS (linear alkylbenzene sulfonate).
Sodium ABS (alkyl benzene sulfonate).
Anionic surfactant with straight-chain alkylate.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an aqueous solution of sodium C14-16 alpha-olefin sulphonate.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provide excellent foaming and detergency properties to a broad spectrum of formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant.

CAS Number: 68439-57-6
EINECS Number: 931-534-0

ClMe2 C6H2OH & C14-16 olefin-SO3Na, p-Chloro-m-xylenol in sodium C14-16 olefin sulfonate, 4 chloro-3,5-dimethyl-phenol; tetradecane-1-sulfonic acid, sodium c14 olefin sulfonate, N816E2SOKI, SCHEMBL1310808, SODIUM C14 OLEFIN SULPHONATE, 2-Tetradecene1-sulfonic acid sodium salt, SODIUM (E)-TETRADEC-2-ENE-1-SULFONATE.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a mixture of long chain sulfonate salts prepared bysulfonation of C14-16 alpha olefins.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) also finds use in textile,printing and dyeing industry, petrochemical products,industrial hard surface cleaning agents.
They produce a high volume of stable and luxurious foam combining the benefits of alkyl ether sulfates and alkyl sulfates in a single product.

In addition, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) have excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is also used as anionic wetting agent in liquid formulations and is a high foaming primary surfactant for handy dishwashing liquids.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be derived from coconut and produces a copious foam.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used as a primary surfactant or mixed with other cleansing agents working to boost the overall detergency of the formulation.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a cleaning agent.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a coconut-based surfactant.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in cosmetics as an anionic surfactant, it produces abundant foam.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) helps keep a surface clean.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) consists chiefly of sodium alkene sulfonates and sodiumhydroxyalkane sulfonates.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used as a primary surfactant or mixed with other cleansing agents working to boost the overall detergency of the formulation.
In addition, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)s have excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.

High active EO-free primary anionic surfactant with hard water and electrolyte tolerance.
Provides rich lather, for use in cleansing products such as body washes and shampoos.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provide excellent foaming and detergency properties to a broad spectrum of formulations.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) produces a high volume of stable and luxurious foam combining the benefits of alkyl ether sulfates and alkyl sulfates in a single product.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.
The powder form is particularly suitable for use in solid and highly concentrated formulations.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) acts as a surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is made primarily from coconut oils.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is stable at a wide pH range and can therefore be used in acidic environments.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is mild primary surfactant with excellent cleansing and degreasing properties.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has good wetting effect, foam booster, slight viscosity enhancer.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is easily compatible with other surfactants including non-ionic, amphoteric or anionic co-surfactants.

Chemically stable in acidic and alkaline conditions.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be used for making sulfate-free cleansing products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an environmentally friendly, biodegradable, aqueous solution of sodium C14-16 alpha olefin sulfonate.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) combines the advantages of high foaming power and good emulsification to make excellent industrial cleaners and car wash products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has hard water and electrolyte tolerance and is stable in acid conditions.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in shower and bath products, shampoo, solid and highly concentrated formulations.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is anionic Surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is air entraining agent, excellent foaming and detergency properties.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used as a mortar and plaster additive in the construction market.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has rich and fine foam.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) especially suitable for non-phosphorus detergents.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) also finds use in textile,printing and dyeing industry, petrochemical products,industrial hard surface cleaning agents.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has a strong wetting and cleaning action and good foaming power.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is also used as anionic wetting agent in liquid formulations and is a high foaming primary surfactant for handy dishwashing liquids.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant often found in bath, shower, and hair care cleansers.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a mixture of long chain sulfonate salts prepared by sulfonation of C14-16 alpha olefins.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be derived from coconut and produces a copious foam.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a mixture of long chain sulfonate salts prepared bysulfonation of C14-16 alpha olefins.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) appears white powder.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant that is derived from coconut oil.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used primarily as a detergent cleansing agent

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is long chain sulfonate salts prepared by the sulfonation of alpha olefins.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in cosmetics and personal care products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an economical.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has an excellent viscosity and flash foaming characteristics with improved mildness in comparison to lauryl sulphates.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has good solvency and compatibility with other surfactants.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provides excellent foaming and detergency properties to a broad spectrum of formulations.

In addition, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) have excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) acts as a olefin sulfonate surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has hard water and electrolyte tolerance and is stable in acid conditions.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) contains sodium benzoate as a preservative.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in shower and bath products, shampoo, solid and highly concentrated formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an aqueous solution of sodium C14-16 alpha-olefin sulphonate.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provides excellent foaming and detergency properties to a broad spectrum of formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) produces a high volume of stable and luxurious foam combining the benefits of alkyl ether sulfates and alkyl sulfates in a single product.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a cleaning agent, or "surfactant," that can also be found in shampoos, shower products and cleaners.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a coconut-based surfactant that offers good cleansing and excellent foaming abilities.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) serves as a surfactant, which means it helps to emulsify and solubilize oils and dirt, allowing them to be washed away.

In products like shampoos and body washes, it contributes to the creation of foam and helps in cleansing.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is derived from the sulfonation of olefins, which are hydrocarbons.
The "C14-16" in the name indicates the carbon chain length of the olefin.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is commonly found in personal care products such as shampoos, body washes, and facial cleansers due to its effective cleansing and foaming properties.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is also used in some household cleaning products like dishwashing detergents.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is often considered milder than some other sulfonate surfactants, making it suitable for use in formulations for sensitive skin.

Many olefin sulfonates are known for their good biodegradability, which is an important consideration in terms of environmental impact.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a great surfactant that helps remove dirt, pollutants and buildup from the hair and scalp.
Mostly present in hair care products, it can also be used in skin care and cosmetics.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a pretty effective cleansing agent with good foaming properties.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) consists chiefly of sodium alkene sulfonates and sodiumhydroxyalkane sulfonates.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be used in shampoo, shower gel, facial cleanser and other cleaning cosmetics, as well as industrial detergent.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) cleans the skin and hair by helping water to mix with oil and dirt so that they can be rinsed away.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a mild anionic, high-foaming & well-emulsifying surfactant.
A versatile and biodegradable cleansing agent with high cleaning power and strong foaming properties.

Unfortunately, these two properties for a surfactant usually mean that it is harsh on the skin, which is the case here as well.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) are a group of anionic surfactants, which are used as detergents.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)s contain a - mostly linear, primary - alkyl R and a monovalent cation M, preferably sodium.

The most frequently used example of this group of substances is sodium α-olefin sulfonate.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used primarily as a detergent cleansing agent, but is potentially drying and can aggravate skin.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a cleaning agent or "surfactant" that is also found in shampoos, bath products and detergents.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) by Innospec acts as a surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has hard water and electrolyte tolerance and is stable in acid conditions.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) contains 2-bromo-2- nitropropane-1,3-diol as a preservative.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in shower and bath products, shampoo, solid and highly concentrated formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an aqueous solution of sodium C14-16 alpha-olefin sulphonate.
Alpha olefin sulfonates provide excellent foaming and detergency properties to a broad spectrum of formulations.

They produce a high volume of stable and luxurious foam combining the benefits of alkyl ether sulfates and alkyl sulfates in a single product.
In addition, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) have excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) use to remove dirt and deposits by surrounding the dirt particles and loosening them from the surface so that they can be rinsed away.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a type of surfactant commonly used in the formulation of personal care and household cleaning products.
Surfactants are compounds that lower the surface tension between two substances, such as a liquid and a solid or between two liquids.
They have both hydrophobic (water-repelling) and hydrophilic (water-attracting) parts, allowing them to interact with both water and oils.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provided as the dried powder.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provide excellent foaming and detergency properties to a broad spectrum of formulations.
They produce a high volume of stable and luxurious foam combining the benefits of alkyl ether sulfates and alkyl sulfates in a single product.

In addition, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)s have excellent hard water and electrolyte tolerance and are stable in acidic conditions, making them ideal for use in all cleaning applications.
The powder form is particularly suitable for use in solid and highly concentrated formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) acts as a surfactant.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has hard water and electrolyte tolerance and is stable in acid conditions.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in shower and bath products, shampoo, solid and highly concentrated formulations.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is mixtures of long chain sulfonate salts prepared by the sulfonation of alpha olefins.

Density: 1.054g/cm3 at 20℃
vapor pressure: 0Pa at 25℃
form: Powder
LogP: -1.3 at 20℃ and pH5.43
Surface tension 36.1mN/m at 1g/L and 20℃
Dissociation constant: 0.15-0.38 at 25℃
EWG's Food Scores: 1-2

The numbers indicate the average lengths of the carbon chains of the alpha olefins.
In cosmetics and personal care products, Sodium Alpha-Olefin Sulfonates are used mainly in shampoos and bath and shower products
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provides excellent foaming and detergency properties to a broad spectrum of formulations.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used primarily as a detergent cleansing agent, but is potentially drying and can aggravate skin.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant that is derived from coconut oil.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is made up of a long chain of sulfonate salts that are prepared by the by-sulfonation of C14-16 olefins.

This ingredient primarily consists of sodium hydroxy alkane sulfonates and sodium alkene sulfonates.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a great surfactant that helps remove dirt, pollutants and buildup from the hair and scalp.
Mostly present in hair care products, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can also be used in skin care and cosmetics.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a pretty effective cleansing agent with good foaming properties
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is produced by sulfonation of alpha-olefins, typically using sulfur trioxide.
Subsequent alkaline hydrolysis gives a mixture of alkene sulfonates (60-65%) and hydroxyalkane sulfonates (35-40%).

The commercially available olefin sulfonates are mostly solutions with about 40% active ingredient content.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an ideal surfactant for a variety of detergent and personal care applications including hand soaps, shampoos, and bath products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) offers the formulator excellent viscosity and foam characteristics, as well as improved mildness over lauryl sulfates, It is more stable than alcohol sulfates over a broad pH range.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) appears white powder.
The chemical formula of NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is C14H27NaO3S.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant that is derived from coconut oil.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is made up of a long chain of sulfonate salts that are prepared by the by-sulfonation of C14-16 olefins.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used primarily as a detergent cleansing agent.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) does produce copious foam.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is added to plenty of hair care and skin care products such as shampoos and cleansers.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is valued for its excellent cleaning abilities.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) helps to remove dirt, oils, and other impurities from surfaces, making it a common ingredient in various cleaning and personal care products.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is compatible with a wide range of other ingredients commonly used in personal care formulations.
This compatibility allows formulators to create stable and effective products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is known for its foaming properties.

In products like shampoos and body washes, it contributes to the development of a rich and stable lather, enhancing the sensory experience during use.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) tends to be stable over a broad pH range.
This stability makes it versatile for use in formulations that may have varying pH levels.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is typically synthesized through the sulfonation of C14-16 olefins.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be derived from coconut.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)’s tricky to include in formulas due to stability issues, but it does produce copious foam.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a highly active, spray-dried material with excellent wetting, foaming and cleaning properties in alkaline, acid or eutral environment and in the presence of metallic salts often found in hard waters.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is for dust control as well as shampoos, hand soaps and bath products. carpet foamer.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in various household and industrial applications such as concrete foamer.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) provides excellent foam and is stable over a wide pH range.
While NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is often considered milder compared to some other sulfonate surfactants, it's still important to be aware that concentrated solutions can potentially cause kin or eye irritation.
However, in the final product at appropriate concentrations, it is generally considered safe for use.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) acts as a good cleansing agent.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) mixes well with water and oil to remove the dust particles settled on the surface of the skin
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an amazing surfactant and a foam forming agent.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) helps the formulations act on the scalp and hair to leave it clean.
Further, the foam helps in easy spreadability of the product throughout..
The numbers indicate the average lengths of the carbon chains of the alpha olefins.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in cosmetics and personal care products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used mainly in shampoos and bath and shower products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant often found in bath, shower, and hair care cleansers.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be derived from coconut.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) produces a copious foam.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an economical.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is versatile Biodegradable surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a high active anionic surfactant.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has an excellent viscosity and flash foaming characteristics with improved mildness in comparison to lauryl sulphates.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has excellent wetting property,detergency, foaming ability and stability,and emulsifying power.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) also has excellent calcium soap dispersibility,hard water resistency.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has good solvency and compatibility with other surfactants.

Surfactants are so-called detergent substances and have a major significance in cosmetics for the cleansing of the skin and hair.
Surfactants are substances which, based on their molecular structure, are able to reduce the surface tension of a liquid.
In this way NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is possible that two actually not mixable substances, such as oil and water, can be finely mixed.

Because of their properties, surfactants have manifold uses in cosmetics: they can cleanse, produce foam and act as emulsifiers and mix substances with one another.
In shampoos, shower gels and soaps, surfactants are, for instance, used to wash fat and soil particles with water off from the body.
Surfactants are also used in toothpaste.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is known for its good compatibility with hard water.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an anionic surfactant often found in bath, shower, and hair care cleansers.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a mixture of long chain sulfonate salts prepared by sulfonation of C14-16 alpha olefins.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is appreciated for its detergent properties.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can effectively break down and lift away oils and greases, making it suitable for use in various cleaning applications.
In hair care products like shampoos, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) helps to remove sebum and other residues from the hair and scalp.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) foaming ability contributes to a satisfying lather during hair washing.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) contributes to the stability of formulations, helping to keep the product's properties consistent over time.
This stability is crucial for maintaining the effectiveness and shelf life of personal care and cleaning products.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)s are generally considered more environmentally friendly compared to some other surfactants.
Their biodegradability and relatively low toxicity are factors that contribute to their eco-friendly profile.
As with any ingredient in personal care or cleaning products, regulatory standards may apply.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is typically used within regulated concentrations to ensure product safety.
Due to its cleansing and foaming properties, this surfactant is commonly found in liquid soaps and body washes, contributing to the overall performance and user experience of these products.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be derived from coconut and produces a copious foam.

Uses:
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in body washes and shower gels for its foaming and cleansing properties.
Helps in removing impurities from the skin, leaving it clean and refreshed.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in bubble bath formulations to create a foaming and luxurious bath experience.

Included in some dishwashing detergents for its degreasing and cleaning properties.
Contributes to the removal of food residues and grease from dishes.
Included in various household cleaning products such as all-purpose cleaners and surface cleaners.
Aids in breaking down and removing dirt and grime from surfaces.

Found in some pet shampoos for NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is cleansing properties, helping to clean and groom the fur.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in industrial cleaning products for its effectiveness in removing oils and contaminants.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in formulations for metal cleaners to help remove oils, greases, and other contaminants from metal surfaces.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be found in some paint strippers where its surfactant properties aid in the removal of paint from surfaces.
In the construction industry, it may be utilized in certain formulations for cleaning and degreasing surfaces, including tools and equipment.
Included in formulations for concrete cleaners to assist in breaking down and removing stains, dirt, and other substances from concrete surfaces.

Used in the printing industry for its wetting properties, helping in the dispersion of inks and cleaning of printing equipment.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in some firefighting foams to generate stable foam for suppressing flammable liquid fires.
The surfactant properties of NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) make it useful in certain formulations for oil spill cleanup, aiding in the dispersion of oil.

Included in some aerosol formulations for its foaming properties, contributing to the spray characteristics of the product.
Found in some formulations for gardening and horticultural products, such as plant washes, where it helps in removing contaminants from plant surfaces.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in water treatment formulations for its ability to disperse and remove organic and oily substances from water.

Found in facial cleansers to aid in the removal of makeup, oils, and other facial impurities.
Contributes to the creation of a lathering texture for a thorough cleanse.
Included in the formulation of liquid hand soaps and other liquid soap products.

Enhances NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate)'s ability to clean hands and surfaces effectively.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a great surfactant that helps remove dirt, pollutants and buildup from the hair and scalp.
Mostly present in hair care products, it can also be used in skin care and cosmetics.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is a pretty effective cleansing agent with good foaming properties.
In its raw form, NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) has the look of a fine white powder.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is added to plenty of hair care and skin care products such as shampoos and cleansers.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) acts as a good cleansing agent.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) mixes well with water and oil to remove the dust particles settled on the surface of the skin.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is an amazing surfactant and a foam forming agent.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) helps the formulations act on the scalp and hair to leave it clean.
Further, the foam helps in easy spreadability of the product throughout
Included in various personal care items such as hand soaps, bath products, and facial cleansers to provide effective cleaning and lathering.

Found in some cosmetics, particularly in products like makeup removers and cleansing wipes, where its surfactant properties aid in the removal of makeup and impurities.
Used in baby shampoos and body washes for its mild cleansing properties, often formulated to be gentle on sensitive skin.
Included in certain medicated shampoos for its role in cleansing the scalp and hair while incorporating therapeutic ingredients.

NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) can be found in some water-based lubricants, contributing to the formulation's texture and ease of application.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used in the textile industry as a wetting agent and detergent in processes such as fabric dyeing and finishing.
Employed in the formulation of adhesives and sealants to enhance their wetting and spreading properties.

Utilized in certain agricultural formulations for its wetting and dispersing properties, aiding in the application of agricultural chemicals.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is sometimes used in oilfield chemicals for applications such as enhanced oil recovery.
Found in emulsion polymerization processes as a surfactant to help stabilize the emulsion and disperse monomers.

Included in some car cleaning products, such as vehicle washes, where its cleansing properties help remove dirt and grime from surfaces.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is used as anionic surfactants in various areas of application due to their pronounced foam formation and foam stability (even with high water hardness), excellent fat-dissolving power and oil dissolving power as well as a favorable ecological profile and low aquatic toxicity and human toxicity.

Safety profile:
The Food and Drug Administration (FDA) reviewed the safety of NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) and approved the use of ammonium, calcium magnesium, potassium and sodium salts of these ingredients (C10-18, with not less than 50% as C14-16)as indirect food additives as components of adhesives and as emulsifiers and/or surface-active agents.
NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) is safe to be used in rinse off products.

However, its concentration should not exceed 2% in leave on formulations.
Sodium C14-6 Olefin Sulfonate can make the skin and hair dry, so it is not recommended for the dry skin types.
Further, Sodium C14-6 Olefin Sulfonate can also be comedogenic and cause acne on highly sensitive skin.

Therefore, a patch test is beneficial prior to full usage.
The CIR Expert Panel evaluated the scientific data and concluded that NANSA LSS 38/AS (Sodium C14-16 Olefin Sulfonate) were safe as used in rinse-off products and safe up to 2% in leave-on products.
The concentration of the gamma sultone impurity of any formulation (leave-on or rinse-off) was limited to unsubstituted alkane sultones at 10 ppm or less; chlorosultones at 1 ppm or less; and unsaturated sultones at 0.1 ppm or less.

Nansa LSS 38/AV is a versatile and aqueous solution of sodium C14-16 alpha-olefin sulfonate.
Nansa LSS 38/AV serves as a powerful olefin sulfonate surfactant.
Nansa LSS 38/AV is renowned for its exceptional foaming capabilities, producing a high volume of stable and luxurious foam.
Nansa LSS 38/AV offers excellent detergency properties, making it highly effective at removing dirt and impurities.

CAS Number: 68439-57-6



APPLICATIONS


Nansa LSS 38/AV is used in shower gel formulations to create rich and foamy lather, offering a luxurious bathing experience.
Nansa LSS 38/AV contributes to bath foam products, producing voluminous bubbles and enhancing relaxation during baths.
In liquid soap formulations, it improves foaming and cleansing properties for effective handwashing.

Nansa LSS 38/AV enhances the lathering and cleaning performance of shampoos, leaving hair refreshed and clean.
Its exceptional foaming capabilities make it an ideal ingredient in bubble bath products for added fun during baths.

Nansa LSS 38/AV is used in solid bar formulations, ensuring effective cleaning in a convenient, solid format.
Nansa LSS 38/AV is suitable for highly concentrated cleaning product formulations, optimizing cleaning power.

Nansa LSS 38/AV contributes to the detergency of laundry detergents, aiding in the removal of stains and dirt from fabrics.
In fabric softeners, it enhances the overall cleaning and softening of clothing and linens.

Nansa LSS 38/AV finds applications in multi-purpose household cleaners, ensuring thorough cleaning of various surfaces.
Nansa LSS 38/AV is used in industrial cleaning products for degreasing and maintenance tasks.

Nansa LSS 38/AV contributes to automotive cleaning products, effectively removing dirt and grime from vehicle surfaces.
In surface disinfectants, it aids in the cleaning and sanitization of frequently touched surfaces.
The chemical is employed in rug and carpet cleaning formulations to remove stains and dirt.

Nansa LSS 38/AV is used in products designed to remove adhesives and sealants in industrial settings.
Nansa LSS 38/AV plays a role in specialty cleaning products for the removal of graffiti, paint, and other coatings.

In electronic device cleaning solutions, it helps clean screens and surfaces without damaging sensitive electronics.
Nansa LSS 38/AV enhances the cleaning performance of floor cleaners, leaving floors spotless.
Nansa LSS 38/AV is used in glass and window cleaning solutions for streak-free and clear surfaces.
Nansa LSS 38/AV contributes to the formulation of janitorial cleaning products used in commercial and institutional settings.

Nansa LSS 38/AV aids in the creation of kitchen and bathroom cleaners, ensuring sanitation and cleanliness.
Nansa LSS 38/AV is used in pool and spa cleaning solutions, maintaining water clarity and hygiene.

Nansa LSS 38/AV helps clean agricultural equipment, facilities, and storage areas in the agricultural industry.
In metal cleaning products, it aids in the maintenance and restoration of metal surfaces.

Nansa LSS 38/AV is used in pressure washing solutions for outdoor surfaces, including siding and decks.
Nansa LSS 38/AV is utilized in aircraft interior cleaning solutions, ensuring the cleanliness and hygiene of airplane cabins.
Nansa LSS 38/AV contributes to boat and marine cleaning products, including hull cleaners and deck washes for marine vessels.
In the oil and gas industry, this chemical aids in cleaning equipment and machinery used in oilfield operations.

Nansa LSS 38/AV is employed in cleaning solutions for construction sites, removing dirt, grime, and construction residues.
Nansa LSS 38/AV helps maintain and clean heavy machinery and equipment used in construction, agriculture, and manufacturing.

Nansa LSS 38/AV is used in products designed to remove rust and scale from metal surfaces in various applications.
Nansa LSS 38/AV enhances the cleaning performance of concrete and driveway cleaners, restoring surfaces to their original condition.
In masonry cleaning products, it assists in cleaning bricks, stones, and concrete surfaces.

Nansa LSS 38/AV aids in the cleaning and maintenance of industrial and automotive parts.
Nansa LSS 38/AV is used in cleaning solutions for mechanical workshops, ensuring equipment and tools are free from contaminants.
Nansa LSS 38/AV contributes to cleaning solutions for agricultural equipment, promoting longevity and efficiency.
In metalworking, it can be incorporated into metalworking fluids for cooling and lubrication.

Nansa LSS 38/AV is used in automotive engine cleaners to remove grease and oil residues.
Nansa LSS 38/AV helps clean concrete formwork, maintaining their quality and extending their lifespan.
In the gardening industry, it is employed in cleaning solutions for maintaining garden equipment.

Nansa LSS 38/AV aids in cleaning and sanitizing sports equipment, ensuring player safety and hygiene.
Nansa LSS 38/AV contributes to cleaning solutions used in healthcare settings for medical equipment maintenance.

Nansa LSS 38/AV ensures the cleanliness and hygiene of restaurant and food service equipment.
It is used in cleaning solutions for buses, trains, and public transportation vehicles.

In electronics manufacturing, the chemical can be part of cleaning solutions for printed circuit boards (PCBs) and components.
Nansa LSS 38/AV aids in the maintenance and cleanliness of various facilities, from offices to factories.

Nansa LSS 38/AV ensures the cleanliness of warehouses and storage areas, facilitating a safe and organized environment.
Nansa LSS 38/AV contributes to cleaning solutions used in hospitals and healthcare facilities, including operating rooms and patient areas.

In the hospitality industry, it is used for cleaning guest rooms, bathrooms, and common areas in hotels.
Nansa LSS 38/AV is a key ingredient in restroom cleaning products for maintaining cleanliness and hygiene in public restrooms.



DESCRIPTION


Nansa LSS 38/AV is a versatile and aqueous solution of sodium C14-16 alpha-olefin sulfonate.
Nansa LSS 38/AV serves as a powerful olefin sulfonate surfactant.
Nansa LSS 38/AV is renowned for its exceptional foaming capabilities, producing a high volume of stable and luxurious foam.
Nansa LSS 38/AV offers excellent detergency properties, making it highly effective at removing dirt and impurities.

Its foaming and detergency benefits combine the advantages of alkyl ether sulfates and alkyl sulfates in a single product.
Nansa LSS 38/AV is ideal for a wide spectrum of formulations due to its compatibility with various ingredients and water conditions.
Nansa LSS 38/AV demonstrates remarkable hard water and electrolyte tolerance, ensuring consistent performance.

Nansa LSS 38/AV maintains stability even in acidic conditions, making it suitable for formulations with lower pH levels.
Sodium benzoate is incorporated into this product as a preservative to extend its shelf life.
In personal care products, such as shower gels and bath foams, it contributes to rich lathering and effective cleansing.

Nansa LSS 38/AV is a preferred choice in shampoo formulations, enhancing both foaming and cleaning properties.
Nansa LSS 38/AV excels in solid formulations, including solid bars and highly concentrated cleaning products.
Nansa LSS 38/AV's foaming properties create a luxurious and satisfying user experience in personal care products.

Its detergency prowess ensures thorough cleaning and the removal of oils, dirt, and residues.
Nansa LSS 38/AV is a versatile ingredient, lending itself to household, personal care, and industrial cleaning products.
In liquid soaps, Nansa LSS 38/AV enhances the foaming and cleaning performance, leaving hands feeling refreshed.
The chemical's stability in various formulations and pH ranges adds flexibility to product development.

For manufacturers, Nansa LSS 38/AV offers ease of incorporation into diverse product formats and formulations.
Nansa LSS 38/AV contributes to the creation of high-quality cleaning solutions for homes and industries.

In personal care, Nansa LSS 38/AV helps achieve a rich and indulgent lather that elevates the bathing experience.
Its compatibility with water conditions and other ingredients makes it a reliable choice for product formulators.

Nansa LSS 38/AV's exceptional foaming properties are particularly desirable in bubble baths and shower products.
Its detergency benefits extend to laundry detergents, ensuring effective stain removal.

Sodium benzoate acts as a safeguard, preserving the product's integrity and efficacy over time.
Overall, Nansa LSS 38/AV is a versatile and high-performing ingredient that enhances the effectiveness and user experience of a wide range of cleaning and personal care products.



FIRST AID


Inhalation:

If inhaled, immediately move the affected person to an area with fresh air.
Allow the person to rest in a comfortable position and keep them warm.
If breathing difficulties persist or if there are signs of respiratory distress, seek immediate medical attention.
If breathing has stopped, perform artificial respiration if trained to do so.


Skin Contact:

In case of skin contact, promptly remove contaminated clothing.
Wash the affected skin area gently but thoroughly with plenty of water and mild soap.
If skin irritation, redness, or rash develops, seek medical attention.
If the chemical is in powder form, carefully brush off excess powder before washing with water.


Eye Contact:

If the chemical comes into contact with the eyes, immediately rinse the affected eye(s) gently with lukewarm, running water for at least 15 minutes.
Hold the eyelids open to ensure thorough rinsing.
Seek immediate medical attention if eye irritation or redness persists or if there is any discomfort.


Ingestion:

If Nansa LSS 38/AV is ingested, do not induce vomiting unless directed to do so by medical professionals.
Rinse out the mouth with water if the person is conscious and able to do so.
Seek immediate medical attention or contact a poison control center.
Provide the medical personnel with detailed information about the ingested substance.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including safety goggles or face shield, chemical-resistant gloves, and protective clothing, when handling Nansa LSS 38/AV.

Ventilation:
Work in a well-ventilated area, or use local exhaust ventilation to control airborne concentrations of the chemical.
Ensure that fumes or vapors are effectively removed from the work area.

Avoid Contact:
Avoid skin and eye contact with the chemical. Use caution to prevent ingestion or inhalation.
Do not eat, drink, or smoke while working with the product.

Handling Precautions:
Handle the chemical with care to prevent spills and splashes.
Use appropriate tools and equipment for transferring or dispensing.

Dust Control:
If the product is in powdered form, minimize dust generation.
Use dust control measures such as dust masks or respirators, and avoid creating airborne dust.

Avoid Mixing:
Do not mix Nansa LSS 38/AV with incompatible chemicals.
Follow recommended formulations and compatibility guidelines.

Labeling:
Ensure that all containers used for transferring or storing the chemical are clearly labeled with the product name, hazard information, and appropriate safety warnings.

Static Electricity:
Take precautions to prevent static electricity buildup, as it may pose a risk in handling powdered forms of the product.

Spills and Leaks:
In the event of a spill, follow appropriate spill response procedures as outlined in the safety data sheet (SDS) and local regulations.
Clean up spills promptly and safely.

Waste Disposal:
Dispose of waste materials, contaminated equipment, or empty containers in accordance with local, regional, and national regulations for hazardous waste disposal.


Storage:

Temperature:
Store Nansa LSS 38/AV within the recommended temperature range as specified in the SDS.
Avoid exposure to extreme temperatures and fluctuations.

Humidity Control:
Maintain proper humidity control to prevent clumping or caking, particularly if the product is in powdered form.

Ventilation:
Ensure that the storage area is well-ventilated to prevent the buildup of fumes or vapors.

Container Sealing:
Keep containers tightly sealed when not in use to prevent moisture absorption and contamination.

Inventory Management:
Implement a first-in, first-out (FIFO) inventory management system to use older stock before newer stock.

Secondary Containment:
Use secondary containment measures such as spill trays or bunds to contain any potential leaks or spills.

Emergency Response:
Have spill control equipment, absorbents, and spill response materials readily available in the storage area.