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Homocystamine is a chemical compound derived from the amino acid homocysteine, which is formed during the metabolism of methionine. It plays a significant role in the one-carbon metabolism pathway and is involved in various physiological processes, including the synthesis of proteins, neurotransmitters, and DNA methylation. Elevated levels of homocysteine and its derivatives, such as homocystamine, have been associated with an increased risk of cardiovascular diseases, neurological disorders, and certain birth defects. The regulation of homocysteine levels is crucial for maintaining overall health, and various factors, including genetics, diet, and lifestyle, can influence its concentration in the body.

463-22-9

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463-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 463-22-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 463-22:
(5*4)+(4*6)+(3*3)+(2*2)+(1*2)=59
59 % 10 = 9
So 463-22-9 is a valid CAS Registry Number.

463-22-9SDS

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 3-(3-aminopropyldisulfanyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names homocysteamine disulfide

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:463-22-9 SDS

463-22-9Relevant academic research and scientific papers

One-pot preparation of coenzyme a analogues via an improved chemo-enzymatic synthesis of pre-CoA thioester synthons

Van Wyk, Marianne,Strauss, Erick

, p. 398 - 400 (2007/10/03)

Coenzyme A analogues are synthesized in a one-pot preparation by biotransformation of pantothenate thioesters through the simultaneous use of three CoA biosynthetic enzymes, followed by aminolysis. The Royal Society of Chemistry.

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