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PINACOLYL METHYLPHOSPHONATE, also known as the chemical warfare agent code GD, is a highly toxic chemical compound primarily used as a nerve agent precursor and a pesticide intermediate. It possesses a high level of toxicity, which can lead to severe symptoms such as nausea, vomiting, convulsions, and respiratory failure, and can be fatal upon exposure. Classified as a schedule 1 chemical under the Chemical Weapons Convention, it has no legitimate use other than for chemical weapon production, posing a significant threat to public health and safety.

616-52-4

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616-52-4 Usage

Uses

Used in Chemical Warfare:
PINACOLYL METHYLPHOSPHONATE is used as a nerve agent precursor for the production of chemical weapons. Its high toxicity and potential to cause severe health effects make it a dangerous substance in the context of warfare.
Used in Pesticide Industry:
PINACOLYL METHYLPHOSPHONATE is used as a pesticide intermediate, contributing to the synthesis of various pesticides. However, its use in this industry is limited due to its classification as a schedule 1 chemical and the associated risks to public health and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 616-52-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 616-52:
(5*6)+(4*1)+(3*6)+(2*5)+(1*2)=64
64 % 10 = 4
So 616-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H29O3P/c1-10(12(3,4)5)15-17(9,14)16-11(2)13(6,7)8/h10-11H,1-9H3

616-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethylbutan-2-yloxy(methyl)phosphinic acid

1.2 Other means of identification

Product number -
Other names pinacolyl hydrogen methylphosphonate

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:616-52-4 SDS

616-52-4Upstream product

616-52-4Downstream Products

616-52-4Relevant academic research and scientific papers

Tripodal molecules for the promotion of phosphoester hydrolysis

Hiscock, Jennifer R.,Sambrook, Mark R.,Cranwell, Philippa B.,Watts, Pat,Vincent, Jack C.,Xuereb, David J.,Wells, Neil J.,Raja, Robert,Gale, Philip A.

supporting information, p. 6217 - 6220 (2014/06/09)

A series of low molecular weight tripodal amide/histidine-containing compounds (1-2) have been synthesised and shown to increase the rate of bis-(p-nitrophenyl) phosphate (BNPP) and soman (GD) breakdown in buffered aqueous solution. This journal is the Partner Organisations 2014.

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

Visible-light C-heteroatom bond cleavage and detoxification of chemical warfare agents using titania-supported gold nanoparticles as photocatalyst

Neau, Tefan,Cojocaru, Bogdan,Parvulescu, Vasile I.,Omoghi, Vasile,Alvaro, Mercedes,Garcia, Hermenegildo

supporting information; scheme or table, p. 4050 - 4054 (2011/07/29)

Gold nanoparticles supported on TiO2 effect the detoxification of soman and VX nerve gases and yperite vesicant agent at room temperature upon visible light illumination.

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