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64436-13-1

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  • Arsonium,(carboxymethyl)trimethyl-, inner salt

    Cas No: 64436-13-1

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64436-13-1 Usage

Uses

Arsenobetaine has been used to investigate the biochemical response of mice (Mus musculus) to inorganic arsenic exposure using liver as the target organ.

Check Digit Verification of cas no

The CAS Registry Mumber 64436-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64436-13:
(7*6)+(6*4)+(5*4)+(4*3)+(3*6)+(2*1)+(1*3)=121
121 % 10 = 1
So 64436-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H11AsO2/c1-6(2,3)4-5(7)8/h4H2,1-3H3

64436-13-1SDS

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 Arsenobetaine

1.2 Other means of identification

Product number -
Other names 2-trimethylarsoniumylacetate

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:64436-13-1 SDS

64436-13-1Synthetic route

trimethylarsine oxide
4964-14-1

trimethylarsine oxide

Iodoacetic acid
64-69-7

Iodoacetic acid

arsenobetaine
64436-13-1

arsenobetaine

Conditions
ConditionsYield
With GLUTATHIONE at 37℃; for 2h; aq. buffer;99%
With methylcobalamin; GLUTATHIONE In water at 37℃; for 94h; pH=7.6; Product distribution / selectivity; Tris-HCl buffer solution;
ethoxycarbonylmethyl(trimethyl)arsonium bromide
64436-12-0

ethoxycarbonylmethyl(trimethyl)arsonium bromide

arsenobetaine
64436-13-1

arsenobetaine

Conditions
ConditionsYield
With ion-exchange resin - form> In water
With Dowex 2 (OH-; water2.5 g
With Dowex 1 x 8 (OH-)
methylcobalamin

methylcobalamin

Dimethylarsinic acid
75-60-5

Dimethylarsinic acid

Iodoacetic acid
64-69-7

Iodoacetic acid

A

arsenobetaine
64436-13-1

arsenobetaine

B

2-dimethylarsinyl acetic acid

2-dimethylarsinyl acetic acid

Conditions
ConditionsYield
With GLUTATHIONE In water at 37℃; for 94h; pH=7.6; Product distribution / selectivity; Tris-HCl buffer solution;

64436-13-1Downstream Products

64436-13-1Relevant articles and documents

COMPOSITION FOR ALKYLATION, AND METHOD FOR DETOXIFICATION OF TOXIC COMPOUND USING THE COMPOSITION

-

Page/Page column 14, (2009/06/27)

It is an object of the present invention to provide a beneficial composition in order to detoxify the harmful compound containing arsenic etc. effectively and systematically and a method for detoxifying a harmful compound by using the composition. The composition for the alkylation according to the present invention is characterized in that the composition contains a cobalt complex. The method of detoxifying the harmful compound according to the present invention is characterized in that a harmful compound containing at least one element selected from the groups comprising arsenic, antimony and selenium is detoxified by the alkylation of the harmful compound, in the presence of the composition according to the present invention.

Synthesis of trimethylated phosphonium and arsonium analogues of the osmoprotectant glycine betaine; contrasted biological activities in two bacterial species

Pichereau, Vianney,Cosquer, Anne,Gaumont, Annie-Claude,Bernard, Theophile

, p. 2893 - 2896 (2007/10/03)

Phosphoniobetaine and arsenobetaine, the P and As analogues of glycine betaine (trimethylammonioacetate) were synthesized and assayed for activity in bacterial osmoprotection biotests, using Escherichia coli and Rhizobium meliloti as model organisms. The P- and As-betaines displayed similar osmoprotective activities in E. coli, but were highly toxic in the betaine- demethylating bacterium R. meliloti.

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