| Revision as of 20:08, 24 June 2008 edit141.189.251.1 (talk)No edit summary← Previous edit | Revision as of 01:44, 29 November 2008 edit undoShrampes (talk | contribs)111 edits n-methyl carbamates addedNext edit → | ||
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| The compound was detected in ]s preserved with ].<ref></ref> | The compound was detected in ]s preserved with ].<ref></ref> | ||
| N-Methyl carbamates are widely used as insecticides.<ref>[http://npic.orst.edu/RMPP/rmpp_ch5.pdf National Pesticide Information Center at Oregon State University</ref> | |||
| ==See also== | ==See also== | ||
Revision as of 01:44, 29 November 2008
Methyl carbamate (also called methylurethane, or urethylane) is an organic compound and the simplest ester of the hypothetical carbamic acid (NH2COOH). Its sum formula is C2H5NO2.
Methyl carbamate is formed by the reaction of ammonia with methyl chloroformate or methyl carbonate. According to US patent number 2834799 urea can be reacted with methanol to form it using boron trifluoride as a reagent. 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. Experimental evidence does show that it is a carcinogen in rat, and not carcinogenic in mice. The compound is "known to the state of California to cause cancer" per Proposition 65.
The compound was detected in wines preserved with dimethyl dicarbonate.
N-Methyl carbamates are widely used as insecticides.
See also
References
- P. Foureman, J.M. Mason, R. Valencia and S. Zimmering, Environ. Mol. Mutagen., 1994, 23 (1), 51 - 63.
- OEHHA
- Inchem.org
- [http://npic.orst.edu/RMPP/rmpp_ch5.pdf National Pesticide Information Center at Oregon State University