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S-Allyl-L-cysteine hydrochloride is a bioactive compound derived from the amino acid L-cysteine, predominantly found in garlic. It possesses antioxidant and anti-inflammatory properties and has been studied for its potential health benefits, such as supporting cardiovascular health, regulating blood pressure, and preventing oxidative damage. Its stability and well-tolerated nature make it a promising candidate for therapeutic applications.

60114-85-4

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60114-85-4 Usage

Uses

Used in Pharmaceutical Industry:
S-Allyl-L-cysteine hydrochloride is used as a therapeutic agent for its potential in treating and preventing various diseases due to its antioxidant and anti-inflammatory properties.
Used in Cardiovascular Health Applications:
S-Allyl-L-cysteine hydrochloride is used as a cardiovascular health supplement to support heart health and help regulate blood pressure.
Used in Antioxidant Formulations:
S-Allyl-L-cysteine hydrochloride is used as an antioxidant in formulations to help prevent oxidative damage and protect against free radicals.
Used in Anti-Inflammatory Treatments:
S-Allyl-L-cysteine hydrochloride is used as an anti-inflammatory agent to reduce inflammation and alleviate symptoms associated with inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 60114-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,1 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60114-85:
(7*6)+(6*0)+(5*1)+(4*1)+(3*4)+(2*8)+(1*5)=84
84 % 10 = 4
So 60114-85-4 is a valid CAS Registry Number.

60114-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3-(Allylthio)-2-aminopropanoic acid hydrochloride

1.2 Other means of identification

Product number -
Other names (2R)-2-amino-3-prop-2-enylsulfanylpropanoic acid,hydrochloride

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:60114-85-4 SDS

60114-85-4Downstream Products

60114-85-4Relevant academic research and scientific papers

Method of manufacturing compds. Allylnaphthol

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Paragraph 0030-0032; 0055; 0062, (2018/06/26)

PROBLEM TO BE SOLVED: To provide a production method of an allyl compound of carrying out the dehydration allylation of a substrate having S, C or N which is a nucleophilic atom, especially S under the presence of a catalyst system consisting of a catalyst precursor having a specific structure and a specific ligand. SOLUTION: The production method of allyl compounds comprises as follow. A catalyst precursor chosen from Formula (1) and Formula (2) and a ligand are mixed, or a catalyst precursor, an allyl alcohol, and a ligand are mixed, then allyl alcohols and a substrate are blended and made to react. The ligand is quinaldic acid or picolinic acid, and the substrate is thiols, thiocarboxylic acids or the like. [Ru(C5H5)(CH3CN)3]PF6(1). [Ru[C5(CH3)5](CH3CN)3]PF6(2). COPYRIGHT: (C)2012,JPOandINPIT

Highly efficient catalytic dehydrative S-allylation of thiols and thioic S-acids

Tanaka, Shinji,Pradhan, Prasun Kanti,Maegawa, Yusuke,Kitamura, Masato

supporting information; experimental part, p. 3996 - 3998 (2010/07/06)

A SH-selective allylation method using [CpRu(2-quinolinecarboxylato) (η3-C3H5)]PF6 has been realized in various solvents including aqueous media to give allyl sulfides and allyl S-thioates, demonstrating the potential applicability to lipopeptide chemistry.

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