64436-13-1 Usage
Description
Arsenobetaine, also known as trimethylarsine oxide, is a naturally occurring organic arsenic compound found in various marine organisms, such as fish and shellfish. It is considered a non-toxic and less harmful form of arsenic compared to inorganic arsenic compounds. Arsenobetaine possesses unique chemical properties, including its ability to bind with biomolecules and its potential to influence biological processes.
Source:
Arsenobetaine is primarily sourced from marine environments, where it is found in the tissues of various marine organisms, including fish and shellfish. ARSENOBETAINE is also present in some freshwater species, although in lower concentrations.
Production Methods:
The production of arsenobetaine is a natural process that occurs within marine organisms as they metabolize inorganic arsenic. The exact mechanisms of arsenobetaine synthesis are not well understood, but it is believed to involve the conversion of inorganic arsenic into a less toxic organic form through a series of biochemical reactions.
Uses
Used in Environmental and Toxicological Research:
Arsenobetaine is used as a research tool to investigate the biochemical response of organisms, such as mice (Mus musculus), to inorganic arsenic exposure. In these studies, the liver is often used as the target organ to assess the effects of arsenic on biological processes and to evaluate the potential toxicity of arsenic compounds.
Used in Biochemical and Nutritional Studies:
Arsenobetaine is also employed in biochemical and nutritional studies to understand the role of arsenic in marine food webs and its potential impact on human health. These studies aim to determine the levels of arsenobetaine in various marine organisms and to evaluate its bioavailability and potential health effects when consumed as part of a diet.
Used in Pharmaceutical and Biomedical Applications:
Although not explicitly mentioned in the provided materials, arsenobetaine has been studied for its potential use in pharmaceutical and biomedical applications. Due to its unique chemical properties and ability to bind with biomolecules, arsenobetaine may have potential as a therapeutic agent or as a component in drug delivery systems.
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
64436-13-1Relevant articles and documents
COMPOSITION FOR ALKYLATION, AND METHOD FOR DETOXIFICATION OF TOXIC COMPOUND USING THE COMPOSITION
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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.