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593-88-4

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593-88-4 Usage

Uses

Trimethylarsine is an environmental pollutant found in lake sediment. Trimethylarsine is toxic to mammalian cells.

Definition

ChEBI: An arsine that is arsane in which each of the hydrogens is substituted by a methyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 593-88-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 593-88:
(5*5)+(4*9)+(3*3)+(2*8)+(1*8)=94
94 % 10 = 4
So 593-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H9As/c1-4(2)3/h1-3H3

593-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylarsine

1.2 Other means of identification

Product number -
Other names AsMe3

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:593-88-4 SDS

593-88-4Relevant articles and documents

Price,Richard

, p. 3209,3210 (1970)

Highly efficient synthesis of trimethylarsine

Gavrilenko,Chekulaeva,Pisareva

, p. 2018 - 2019 (1996)

A convenient, highly efficient, and environmentally safe procedure for the preparation of trimethylarsine was proposed. A quantitative yield of this compound in the reaction of As2O3 with AlMe3 was attained for the first time by using mechanochemical activation of the process.

Claeys

, p. 446,449 (1966)

Synthesis of a Homologous Series of Trialkyl Arsines (C3-C12) and Applications of Arsenic Triiodide as a Synthetic Precursor

Ligiéro, Carolina B.P.,Francisco, Marcos A.S.,Gama, Michelle S.,Carbonezi, Carlos A.,Leocadio, Isabela C.L.,de Souza, Wladmir F.,Esteves, Pierre M.

, p. 912 - 916 (2021/03/17)

This work presents some modifications in the post-synthetic processing for a classical arsenic reagent: AsI3. In comparison with the widely used analog, the trichloride, arsenic triiodide presents several advantages such as low toxicity, air stability, and low volatility. It was used as a synthetic precursor in the preparation of a variety of arsenic(III) derivatives like arsines, arsenites, and thioarsenites. Besides that, AsI3 was submitted to a diversity-oriented Grignard reaction in the preparation of a homologous series of trialkyl arsines ranging from AsC3H9 to AsC12H27. The series was analyzed by comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry to provide a trialkyl arsines library that can be used for the direct analysis of natural samples.

Trialkyl Group VA metal compounds

-

, (2008/06/13)

Disclosed are methods of preparing trialkyl Group VA metal compounds in high yield and high purity. Such trialkyl Group VA metal compounds are substantially free of oxygenated impurities, ethereal solvents and metallic impurities.

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