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Isobutyl hydrogen methylphosphonate is an organophosphorus compound with the chemical formula C4H11O2P. It is a colorless liquid with a slight odor and is soluble in water. This chemical is primarily used as an intermediate in the synthesis of various pesticides and chemical warfare agents, such as the nerve agent VX. Due to its potential use in the production of harmful substances, it is subject to strict regulations and control measures in many countries. Isobutyl hydrogen methylphosphonate is also known for its potential environmental and health risks, as it can be toxic to aquatic life and may cause respiratory and skin irritation in humans.

1604-38-2

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1604-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1604-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1604-38:
(6*1)+(5*6)+(4*0)+(3*4)+(2*3)+(1*8)=62
62 % 10 = 2
So 1604-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H13O3P/c1-5(2)4-8-9(3,6)7/h5H,4H2,1-3H3,(H,6,7)

1604-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl(2-methylpropoxy)phosphinic acid

1.2 Other means of identification

Product number -
Other names Methylphosphonic acidisobutyl ester

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:1604-38-2 SDS

1604-38-2Relevant academic research and scientific papers

VARIANTS OF PHOSPHOTRIESTERASE FOR THE HYDROLYSIS AND DETOXIFICATION OF NERVE AGENTS

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Paragraph 0199, (2016/05/24)

Variants of phosphotriesterase have been created that exhibit enhanced hydrolysis of V-type and G-type nerve agents over wild-type phosphotriesterase. V- and G-type nerve agents have an SP and RP enantiomer. The SP enantiomers are more toxic. V-type nerve

Molecular engineering of organophosphate hydrolysis activity from a weak promiscuous lactonase template

Meier, Monika M.,Rajendran, Chitra,Malisi, Christoph,Fox, Nicholas G.,Xu, Chengfu,Schlee, Sandra,Barondeau, David P.,Hoecker, Birte,Sterner, Reinhard,Raushel, Frank M.

supporting information, p. 11670 - 11677 (2013/09/02)

Rapid evolution of enzymes provides unique molecular insights into the remarkable adaptability of proteins and helps to elucidate the relationship between amino acid sequence, structure, and function. We interrogated the evolution of the phosphotriesteras

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