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| Product Name: | XMC | | Synonyms: | XMC;XMC emulsion;XMC STANDARD;3,5-dimethyl-phenomethylcarbamate;3,5-Dimethylphenyl Methylcarbamate;3,5-Dimethylphenyl N-methylcarbamate;3,5-dimethylphenylmethylcarbamate;3,5-dimethylphenyln-methylcarbamate | | CAS: | 2655-14-3 | | MF: | C10H13NO2 | | MW: | 179.22 | | EINECS: | | | Product Categories: | Pharmaceutical Raw Materials | | Mol File: | 2655-14-3.mol |  |
| Melting point | 101-102℃ (toluene pentane ) | | Boiling point | 311.75°C (rough estimate) | | density | 0.54 g/cm3 | | vapor pressure | 6.8 x 10-3 Pa (25 °C) | | refractive index | 1.5150 (estimate) | | storage temp. | 0-6°C
| | pka | 12.38±0.46(Predicted) | | Water Solubility | 470 mg l-1 (20 °C) | | CAS DataBase Reference | 2655-14-3 | | EPA Substance Registry System | Phenol, 3,5-dimethyl-, 1-(N-methylcarbamate) (2655-14-3) |
| Uses | XMC is an insecticide with primarily contact action. It is mainly
used to control leafhoppers and planthoppers on rice, and tea green leafhoppers
on tea. | | Uses | XMC (pesticide) is a pesticide used in pesticide formulation for the protection of green tea crops. | | Definition | ChEBI: XMC is a carbamate ester. It has a role as a carbamate insecticide, an EC 3.1.1.7 (acetylcholinesterase) inhibitor and an agrochemical. It is functionally related to a methylcarbamic acid and a 3,5-xylenol. | | Metabolic pathway | Metabolic pathways for XMC involve hydroxylation of ring-methyl
groups, N-methyl groups and of the phenyl ring. Hydrolysis of the ester
moiety occurs in soils. | | Degradation | XMC is rapidly hydrolysed in alkaline media to afford the phenol (2). It is
relatively stable in neutral and weakly acidic aqueous solutions even at
temperatures up to 90 °C. Aqueous solutions of XMC are stable to light(PM). |
| | XMC Preparation Products And Raw materials |
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