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N-Methylcarbamic acid butyl ester, also known as butocarboxim, is an organophosphate compound commonly used as an insecticide. It works by inhibiting the enzyme acetylcholinesterase, which is essential for the proper functioning of the nervous system in insects. This inhibition leads to the accumulation of acetylcholine, causing overstimulation and ultimately death in the target pests. The chemical is effective against a wide range of insects, including aphids, whiteflies, and mites, and is used in agriculture to protect crops from damage. However, due to its potential harm to non-target organisms and the environment, its use is regulated in many countries.

5461-30-3

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5461-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5461-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5461-30:
(6*5)+(5*4)+(4*6)+(3*1)+(2*3)+(1*0)=83
83 % 10 = 3
So 5461-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-3-4-5-9-6(8)7-2/h3-5H2,1-2H3,(H,7,8)

5461-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl N-methylcarbamate

1.2 Other means of identification

Product number -
Other names Butyl N-methyl carbamate

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:5461-30-3 SDS

5461-30-3Downstream Products

5461-30-3Relevant articles and documents

Process for the preparation of aryl esters of N-alkyl carbamic acids

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, (2008/06/13)

Aryl esters of N-alkyl carbamic acids are prepared by reacting an alkyl N-alkyl carbamate of the general formula R1 - NH - COO - R3 wherein R1 and R3 are both alkyl groups with a substituted phenol in the presence of a halogen-containing phosphorus compound to produce the desired ester of the formula R1 -NH - COOR2 wherein R1 is an alkyl group and R2 is an aryl group.

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