Methyl carbamate

Methyl carbamate
Names
IUPAC name
Methyl carbamate
Identifiers
598-55-0 N
3D model (Jmol) Interactive image
ChEBI CHEBI:76606 N
ChEMBL ChEMBL1085707 YesY
ChemSpider 11229 YesY
ECHA InfoCard 100.009.037
KEGG C19445 N
PubChem 11722
Properties
C2H5NO2
Molar mass 75 g/mol
Appearance white solid
Density 1.136 (56 °C)
Melting point 52 °C (126 °F; 325 K)
Boiling point 177 °C (351 °F; 450 K)
good
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Methyl carbamate (also called methylurethane, or urethylane) is an organic compound and the simplest ester of carbamic acid (H2NCO2H). It is a colourless solid.[1]

Methyl carbamate is prepared by the reaction of methanol and urea:

CO(NH2)2 + CH3OH → CH3OC(O)NH2 + NH3

It also forms in the reaction of ammonia with methyl chloroformate or dimethyl carbonate.

Safety and occurrence

Unlike its close relative ethyl carbamate it is not mutagenic in Salmonella (it tested negative in the Ames test), but it is mutagenic in Drosophila.[2] Experimental evidence does show that it is a carcinogen in rats, and not carcinogenic in mice. The compound is "known to the state of California to cause cancer" per Proposition 65.[3]

Production, use, and exposure

The compound was detected in wines preserved with dimethyl dicarbonate.[4]

Methyl carbamate is used primarily in the textile and polymer industries as a reactive intermediate. In the textile industry, it is used in the manufacture of dimethylol methyl carbamate-based resins that are applied on polyester cotton blend fabrics as durable-press finishes. The treated fabrics have good crease-angle retention, resist acid souring in commercial laundries, do not retain chlorine, and have flame-retardant properties. Methyl carbamate also is used in the manufacture of pharmaceuticals, insecticides, and urethane.[5]

N-Methyl carbamates are widely used as insecticides.[6] They have anticholinesterase activity without a cumulative effect.

See also

References

  1. ↑ Jäger, Peter; Rentzea, Costin N.; Kieczka, Heinz (2005), "Carbamates and Carbamoyl Chlorides", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a05_051
  2. ↑ Foureman, P.; Mason, J. M.; Valencia, R.; Zimmering, S. (1994). Environ. Mol. Mutagen. 23 (1): 51–63. Missing or empty |title= (help)
  3. ↑ OEHHA
  4. ↑ Inchem.org
  5. ↑ National Toxocology Program
  6. ↑ National Pesticide Information Center at Oregon State University
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