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Diethylarsinic acid, also known as (diethylamino)arsinic acid, is an organoarsenic compound with the chemical formula C4H11AsO3. It is a colorless, crystalline solid that is soluble in water and has a molecular weight of 180.03 g/mol. Diethylarsinic acid is formed by the reaction of arsenic acid with diethylamine and is used in the synthesis of various organoarsenic compounds. Diethylarsinic acid has potential applications in the pharmaceutical industry and as a chemical intermediate. However, due to its arsenic content, it is considered toxic and requires proper handling and disposal to minimize environmental and health risks.

4964-27-6

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4964-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4964-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4964-27:
(6*4)+(5*9)+(4*6)+(3*4)+(2*2)+(1*7)=116
116 % 10 = 6
So 4964-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11AsO2/c1-3-5(6,7)4-2/h3-4H2,1-2H3,(H,6,7)

4964-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylarsinic acid

1.2 Other means of identification

Product number -
Other names Diaethylarsinigsaeure

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

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More Details:4964-27-6 SDS

4964-27-6Downstream Products

4964-27-6Relevant articles and documents

Kinetics of the Aminolysis of Ethyl p-Nitrophenyl Carbonate in the Presence of Dodecylammonium Diethylarsinate Aggregates in Chloroform. Complex Effects of Solubilized Water

Seoud, Monica I. El,Seoud, Omar A. El

, p. 2686 - 2690 (1981)

The kinetics of the aminolysis of ethyl p-nitrophenyl carbonate (ENPC) by dodecylamine (DA), dodecylammonium diethylarsinate (DADEA; dry aggregates and in the presence of solubilized water), and DA plus dry DADEA in chloroform were studied spectrophotomet

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