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N-Methylacetamide

N-Methylacetamide
N-Methylacetamide structure
CAS No.
79-16-3
Chemical Name:
N-Methylacetamide
Synonyms
NMA;dpgs;X 44;CH3CONHCH3;N-MethylacetaM;ACETMETHYLAMIDE;methyl-acetamid;Methylacetamide;N-METHYLACETAMIDE;ACETYLMETHYLAMINE
CBNumber:
CB2302560
Molecular Formula:
C3H7NO
Formula Weight:
73.09
MOL File:
79-16-3.mol

N-Methylacetamide Properties

Melting point:
26-28 °C(lit.)
Boiling point:
204-206 °C(lit.)
Density 
0.957 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.433(lit.)
Flash point:
227 °F
storage temp. 
Store below +30°C.
solubility 
miscible with ethanol, ether, acetone, water, chloroform, benzene
PH
7 (H2O)
explosive limit
3.2-18.1%(V)
Water Solubility 
soluble
BRN 
1071255
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey
OHLUUHNLEMFGTQ-UHFFFAOYSA-N
CAS DataBase Reference
79-16-3(CAS DataBase Reference)
NIST Chemistry Reference
Acetamide, N-methyl-(79-16-3)
EPA Substance Registry System
Acetamide, N-methyl-(79-16-3)
SAFETY
  • Risk and Safety Statements
  • Hazard and Precautionary Statements (GHS)
Hazard Codes  T
Risk Statements  61
Safety Statements  53-45
WGK Germany  2
RTECS  AC5960000
TSCA  Yes
HS Code  29241900
Hazardous Substances Data 79-16-3(Hazardous Substances Data)
Symbol(GHS):
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning P264, P280, P305+P351+P338,P337+P313P
H360 May damage fertility or the unborn child Reproductive toxicity Category 1A, 1B Danger
Precautionary statements:
P201 Obtain special instructions before use.
P202 Do not handle until all safety precautions have been read and understood.
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313 IF exposed or concerned: Get medical advice/attention.
P405 Store locked up.
P501 Dispose of contents/container to..…

N-Methylacetamide price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M26305 N-Methylacetamide ≥99% 79-16-3 5g $21.4 2018-11-13 Buy
Sigma-Aldrich M26305 N-Methylacetamide ≥99% 79-16-3 100g $24.2 2018-11-13 Buy
TCI Chemical M0133 N-Methylacetamide >99.0%(GC) 79-16-3 25g $14 2018-11-22 Buy
TCI Chemical M0133 N-Methylacetamide >99.0%(GC) 79-16-3 250g $32 2018-11-22 Buy
Alfa Aesar A17928 N-Methylacetamide, 99% 79-16-3 250g $28.2 2018-11-13 Buy

N-Methylacetamide Chemical Properties,Uses,Production

Chemical Properties

colourless liquid or solid

Definition

ChEBI: A monocarboxylic acid amide that is the N-methyl derivative of 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.]

N-Methylacetamide Preparation Products And Raw materials

Raw materials

Preparation Products


N-Methylacetamide Suppliers

Global( 208)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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View Lastest Price from N-Methylacetamide manufacturers

Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
2018-12-17 N-Methylacetamide
79-16-3
US $1.00 / kg 1kg 99% 1000kg career henan chemical co

N-Methylacetamide Spectrum


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