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N-methylcarbamate is a chemical compound derived from carbamic acid, known for its effectiveness as a pesticide and insecticide.
Used in Agriculture:
N-methylcarbamate is used as a pesticide for controlling a wide range of agricultural pests. It works by inhibiting the activity of the enzyme acetylcholinesterase in insects, leading to the accumulation of acetylcholine, paralysis, and ultimately death.
Used in Regulatory Frameworks:
N-methylcarbamate is subject to strict regulations and guidelines due to its associated toxicity in non-target organisms, including humans. These measures aim to minimize the environmental and health risks associated with its use.

6414-57-9

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6414-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6414-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6414-57:
(6*6)+(5*4)+(4*1)+(3*4)+(2*5)+(1*7)=89
89 % 10 = 9
So 6414-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H5NO2/c1-3-2(4)5/h3H,1H3,(H,4,5)/p-1

6414-57-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methylcarbamic acid

1.2 Other means of identification

Product number -
Other names N-Methylformohydroxamic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6414-57-9 SDS

6414-57-9Downstream Products

6414-57-9Relevant academic research and scientific papers

Influence of micelles on the basic degradation of carbofuran

Arias, Manuel,Garcia-Rio, Luis,Mejuto, Juan C.,Rodriguez-Dafonte, Pedro,Simal-Gandara, Jesus

, p. 7172 - 7178 (2007/10/03)

The effect of micellar aggregates upon the stability of carbofuran in basic media has been studied. The effect of the presence of micelles upon the basic hydrolysis of carbofuran is a function of the nature of the surfactant monomer. Important catalysis of basic hydrolysis of carbofuran in the presence of colloid aggregates with positive surface charge has been reported. On the other hand, the presence of anionic and nonionic surfactants implies a large inhibition of the basic hydrolysis of carbofuran. Both catalysis and inhibition are due to the association of carbofuran with the micellar core. The kinetic constants for the basic hydrolysis of carbofuran in these microheterogeneous media have been obtained on the basis of a micellar pseudophase model. No significant changes in the intrinsic reactivity of HO- against carbofuran have been observed.

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