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624-01-1

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624-01-1 Usage

Description

5-Oxodecanoic acid, also known as 5-oxodecanoate or 5-oxo-decanoate, is a fatty acid derivative with the chemical formula C10H18O3. It is a member of the oxo fatty acid family, characterized by the presence of a ketone group at the 5th carbon atom. 5-Oxodecanoic acid is formed through the oxidative degradation of unsaturated fatty acids and can also be produced through the metabolism of xenobiotics by microorganisms. 5-Oxodecanoic acid has been studied for its potential role in inflammation and immune response, as well as its potential use as a biomarker for certain metabolic disorders. It may also have applications in the development of pharmaceuticals and other industrial products.

Uses

Used in Pharmaceutical Development:
5-Oxodecanoic acid is used as a potential therapeutic agent for modulating inflammation and immune response. Its unique structure and properties allow it to interact with biological systems, making it a promising candidate for the development of new drugs targeting inflammatory and immune-related disorders.
Used in Biomarker Research:
5-Oxodecanoic acid is used as a potential biomarker for certain metabolic disorders. Its presence and levels in biological samples can provide valuable information about the metabolic status and health of an individual, aiding in the diagnosis and monitoring of various conditions.
Used in Industrial Applications:
5-Oxodecanoic acid is used as a building block or intermediate in the synthesis of other organic compounds and materials. Its unique chemical properties make it suitable for use in the development of new industrial products, such as specialty chemicals, polymers, and surfactants.
Used in Nutritional Research:
5-Oxodecanoic acid is used as a subject of nutritional research to better understand its role in metabolism and its potential impact on health. Studies on its effects on lipid metabolism, energy balance, and other physiological processes can contribute to the development of novel nutritional strategies and interventions.
Used in Cosmetics and Personal Care Products:
5-Oxodecanoic acid may be used as an ingredient in cosmetics and personal care products due to its potential benefits for skin health and its ability to modulate inflammation. Its incorporation into formulations can provide anti-inflammatory and skin-conditioning properties, enhancing the efficacy and safety of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 624-01-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 624-01:
(5*6)+(4*2)+(3*4)+(2*0)+(1*1)=51
51 % 10 = 1
So 624-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O3/c1-2-3-4-6-9(11)7-5-8-10(12)13/h2-8H2,1H3,(H,12,13)

624-01-1SDS

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 5-Oxodecanoic acid

1.2 Other means of identification

Product number -
Other names 5-oxo-decanoic acid

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:624-01-1 SDS

624-01-1Relevant articles and documents

A new environmentally benign catalytic process for the asymmetric synthesis of lactones: Synthesis of the flavouring δ-decalactone molecule

Corma, Avelino,Iborra, Sara,Mifsud, Mari?a,Renz, Michael,Susarte, Manuel

, p. 257 - 262 (2007/10/03)

The system Sn-Beta/hydrogen peroxide is applied to the Baeyer-Villiger oxidation of delfone to δ-decalactone, which is an industrial fragrance. The reaction is carried out without solvent and with a substrate/catalyst ratio > 200 (wt/wt). Starting with an enantiomerically enriched delfone it is shown that the rearrangement occurs with retention of configuration at the migrating asymmetric carbon atom, and enantiomerically enriched δ-decalactone is obtained as product. This process offers clear advantages over the actual industrial production that uses peracids as oxidants.

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