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5-Carboxypentyl disulfide, with the molecular formula C7H12O4S2, is a disulfide derivative that plays a significant role in organic synthesis and biochemical research. Its primary function is to modify proteins and peptides, making it a valuable component in the development of pharmaceuticals and other organic compounds. 5-CARBOXYPENTYL DISULFIDE also holds promise for new drug development and the study of oxidative stress and its impact on biological systems. Furthermore, 5-carboxypentyl disulfide may serve as a potential biomarker for medical conditions related to the oxidative stress pathway.

92038-67-0

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92038-67-0 Usage

Uses

Used in Organic Synthesis:
5-Carboxypentyl disulfide is used as a modifying agent for proteins and peptides, enabling the development of new pharmaceuticals and organic compounds.
Used in Biochemical Research:
In biochemical research, 5-Carboxypentyl disulfide is utilized as a tool to study the effects of oxidative stress on biological systems, contributing to a better understanding of related medical conditions.
Used in Pharmaceutical Development:
5-Carboxypentyl disulfide is employed in the development of new drugs, potentially offering novel therapeutic options for various medical conditions.
Used as a Biomarker:
5-Carboxypentyl disulfide may be used as a biomarker for various medical conditions associated with the oxidative stress pathway, aiding in diagnosis and treatment monitoring.

Check Digit Verification of cas no

The CAS Registry Mumber 92038-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 92038-67:
(7*9)+(6*2)+(5*0)+(4*3)+(3*8)+(2*6)+(1*7)=130
130 % 10 = 0
So 92038-67-0 is a valid CAS Registry Number.

92038-67-0SDS

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 6-(5-carboxypentyldisulfanyl)hexanoic acid

1.2 Other means of identification

Product number -
Other names 7,8-Dithia-tetradecandisaeure

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:92038-67-0 SDS

92038-67-0Downstream Products

92038-67-0Relevant academic research and scientific papers

Sulfur transfer reactions of tetrathiomolybdate in water: Synthesis of alkyl disulfides from alkyl halides

Ilankumaran, Palanichamy,Prabhu, Kandikere R.,Chandrasekaran, Srinivasan

, p. 4031 - 4034 (2007/10/03)

Reaction of a number of alkyl halides with tetrathiomolybdate in water as the solvent affords the corresponding disulfides in good yields.

Kinetics of Intramolecular Alkyl Radical Attack on Sulfur in Disulfides and Thioesters

Beckwith, Athelstan L. J.,Duggan, Sandhya A. M.

, p. 1509 - 1518 (2007/10/02)

The 4-(alkyldithio)butyl radicals 8a and c, and the 4-(phenyldithio)butyl radical 8b, generated from the corresponding esters of N-hydroxypyridine-2(1H)-thione, undergo fast exo-cyclisation by SHi attack at sulfur.Similarly, the 5-(alkyldithio)pentyl radical 8d undergoes 1,6-ring formation.The rate constants for cyclisation were determined by photolysis of the radical precursors in the presence of appropriate thiols.Butyl and pentyl radicals bearing ω-acetylthio or ω-benzoylthio substituents also undergo ring closure but much more slowly.The kinetics of these intramolecular SH2 reactions are discussed and compared with those for the intermolecular attack of hexyl radicals on diphenyl disulfide and on dibutyl disulfide.

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