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N-Methylacetamide

CAS No.
79-16-3
Chemical Name:
N-Methylacetamide
Synonyms
NMA;Methylacetamide;CH3CONHCH3;dpgs;X 44;N-MethylacetaM;ACETMETHYLAMIDE;methyl-acetamid;N-METHYLACETAMIDE;ACETYLMETHYLAMINE
CBNumber:
CB2302560
Molecular Formula:
C3H7NO
Lewis structure
ch3conhch3 lewis structure
Molecular Weight:
73.09
MDL Number:
MFCD00008683
MOL File:
79-16-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-10 10:27:08
Product description Number Pack Size Price
N-Methylacetamide ≥99% M26305 5g $40
N-Methylacetamide ≥99% M26305 100g $50.3
N-Methylacetamide >99.0%(GC) M0133 25g $19
N-Methylacetamide >99.0%(GC) M0133 250g $42
N-Methylacetamide ≥99% M26305 500g $93.6
More product size

N-Methylacetamide Properties

Melting point 26-28 °C (lit.)
Boiling point 204-206 °C (lit.)
Density 0.957 g/mL at 25 °C (lit.)
vapor pressure 12-3680Pa at 15-113℃
refractive index n20/D 1.433(lit.)
Flash point 227 °F
storage temp. Inert atmosphere,Room Temperature
solubility miscible with ethanol, ether, acetone, water, chloroform, benzene
pka 16.61±0.46(Predicted)
form Solid
color Colourless
PH 7 (H2O)
explosive limit 3.2-18.1%(V)
Water Solubility soluble
BRN 1071255
Henry's Law Constant 2.1×103 mol/(m3Pa) at 25℃, Burkholder et al. (2019)
Dielectric constant 178.90000000000001
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
Cosmetics Ingredients Functions NOT REPORTED
InChI 1S/C3H7NO/c1-3(5)4-2/h1-2H3,(H,4,5)
InChIKey OHLUUHNLEMFGTQ-UHFFFAOYSA-N
SMILES CNC(C)=O
LogP -1.05--0.7 at 25℃
Surface tension 34.13mN/m at 293.15K
Substances of Very High Concern (SVHC) Candidate List N-methylacetamide (79-16-3)
CAS DataBase Reference 79-16-3(CAS DataBase Reference)
FDA UNII V0T777481M
NIST Chemistry Reference Acetamide, N-methyl-(79-16-3)
EPA Substance Registry System N-Methylacetamide (79-16-3)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H360D
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T
Risk Statements  61
Safety Statements  53-45
WGK Germany  2
RTECS  AC5960000
TSCA  TSCA listed
HS Code  29241900
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Repr. 1B
Hazardous Substances Data 79-16-3(Hazardous Substances Data)
Toxicity LD50 oral in rat: 5gm/kg
NFPA 704
1
0 0

N-Methylacetamide price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M26305 N-Methylacetamide ≥99% 79-16-3 5g $40 2026-04-30 Buy
Sigma-Aldrich M26305 N-Methylacetamide ≥99% 79-16-3 100g $50.3 2026-04-30 Buy
TCI Chemical M0133 N-Methylacetamide >99.0%(GC) 79-16-3 25g $19 2026-04-30 Buy
TCI Chemical M0133 N-Methylacetamide >99.0%(GC) 79-16-3 250g $42 2026-04-30 Buy
Sigma-Aldrich M26305 N-Methylacetamide ≥99% 79-16-3 500g $93.6 2026-04-30 Buy
Product number Packaging Price Buy
M26305 5g $40 Buy
M26305 100g $50.3 Buy
M0133 25g $19 Buy
M0133 250g $42 Buy
M26305 500g $93.6 Buy

N-Methylacetamide Chemical Properties,Uses,Production

Chemical Properties

colourless liquid or solid. Soluble in water, ethanol, benzene, ether, chloroform, insoluble in petroleum ether.

Uses

N-Methylacetamide is used as a chemical intermediate in the production of life science, agrochemicals, electronic materials and construction materials. It is also used as a solvent, in electrochemistry.

Definition

ChEBI: N-methylacetamide is a monocarboxylic acid amide that is the N-methyl derivative of acetamide. It has a role as a metabolite. It is a member of acetamides and a monocarboxylic acid amide. It is functionally related to an acetamide.

Production Methods

Af-Methylacetamide has been prepared by reaction of methylamine with hot acetic acid (D'Alelio and Reid, 1937) and with acetic anhydride (Mauger and Soper, 1946). Other methods include heating iV,N-dimethylurea with acetic acid (US Patent, 1936) and reduction/hydrogenation of N-(hydroxymethyl)acetamide (US Patent, 1944).

Industrial uses

Even though N-methylacetamide shares many general physical and chemical properties with dimethylacetamide, it has not found the extensive industrial applications of the latter. N-methylacetamide dissolves many inorganic salts.

Safety Profile

Moderately toxic by intraperitoneal and subcutaneous routes. Mddly toxic by ingestion and intravenous routes. An experimental teratogen. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Metabolism

In a recent comparative toxicity and metabolism study on four formamides and on N-methylacetamide, the sole metabolite of N-methylacetamide in the urine of mice was identified as N-(hydroxymethyl)acetamide (Kestell et al 1987). There was no evidence of induction of hepatic drug metabolizing enzymes in rats following treatment with N-methylacetamide (Ackerman and Leibman, 1977). N-Methylacetamide influenced neither the sleeping time induced by hexobarbital nor the metabolism of hexobarbital or aniline.

Purification Methods

Fractionally distil it under vacuum, then fractionally crystallise it twice from its melt. Likely impurities include acetic acid, methyl amine and H2O. For a detailed purification procedure, see Knecht and Kolthoff, Inorg Chem 1 195 1962. Although N-methylacetamide is commercially available it is often extensively contaminated with acetic acid, methylamine, water and an unidentified impurity. The recommended procedure is to synthesise it in the laboratory by direct reaction. The gaseous amine is passed into hot glacial acetic acid, to give a partially aqueous solution of methylammonium acetate which is heated to ca 130o to expel water. Chemical methods of purification such as extraction by pet ether, treatment with H2SO4, K2CO3 or CaO can be used but are more laborious. Tests for purity include the Karl Fischer titration for water; this can be applied directly. Acetic acid and methylamine can be detected polarographically. In addition to the above, purification of N-methylacetamide can be achieved by fractional freezing, including zone melting, repeated many times, or by vacuum distillation under reduced pressures. For details of zone melting techniques, see Knecht in Recommended Methods for Purification of Solvents and Tests for Impurities, Coetzee Ed. Pergamon Press 1982.[Beilstein 4 IV 176.]

1445-45-0
593-51-1
79-16-3
Synthesis of N-Methylacetamide from Trimethyl orthoacetate and Methylamine hydrochloride
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View Lastest Price from N-Methylacetamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-Methylacetamide pictures 2026-05-03 N-Methylacetamide
79-16-3
US $1.00 / g 1g 99% 1000kg RongNa Biotechnology Co.,Ltd
N-Methylacetamide pictures 2026-03-20 N-Methylacetamide
79-16-3
US $10.00 / kg 1kg 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
N-Methylacetamide pictures 2026-02-02 N-Methylacetamide
79-16-3
US $0.00-0.00 / KG 5mg 99% HPLC 2000tons Shaanxi Dideu Medichem Co. Ltd
LABOTEST-BB LT00779190 dimethylcarboxamide ACETYL METHYLAMIDE ACETYLMETHYLAMINE ACETMETHYLAMIDE ACETIC ACID METHYLAMIDE NMA N-METHYLACETAMIDE N-ACETYLMETHYLAMINE N-ACETYL-N-METHYLAMINE Acetamide,N-methyl- N-METHYLACETAMIDE, 99+% N-Methylacetylamine N-METHYLACETAMIDE(NMA) N-MethylAcetylamide 1-(Methylimino)ethanol dpgs Methylacetylamine N-MethylacetaMide, 99+% 100GR N-MethylacetaMide, 99+% 500GR N - Methyl ethyl aMide N-MethylacetaM Acetylmethylamine N-Acetyl-N-methylamine aceticacid,amide,n-methyl Acetylmethylammine CH3CONHCH3 methyl-acetamid Methylacetamide Monomethylacetamide n-methyl-acetamid N-Methylethanamide n-monomethylacetamide X 44 N-Methylacetamide> N-Methylacetamide ISO 9001:2015 REACH N-Methylacetamide 79-16-3 Brexpiprazole Impurity 131 N-Methylacetamide N-MethylAcetylamide/N-Methylacetamide 79-16-3 Nitrogen Compounds Organic Building Blocks Protected Amines Building Blocks Building Blocks Chemical Synthesis Nitrogen Compounds Organic Building Blocks Protected Amines 79-16-3