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56618-58-7

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56618-58-7 Usage

Description

3-Hydroxycapric acid methyl ester, also known as the methyl ester of one of the two major components of bacterial Lipid A, is a colorless oil with unique chemical properties. It is derived from 3-hydroxycapric acid, which is a medium-chain hydroxy acid, and is known for its various applications across different industries.

Uses

Used in Pharmaceutical Industry:
3-Hydroxycapric acid methyl ester is used as an active pharmaceutical ingredient for its potential therapeutic effects. It is particularly valuable in the development of drugs targeting bacterial infections, as it is derived from a component of bacterial Lipid A, which plays a crucial role in the pathogenesis of such infections.
Used in Cosmetics Industry:
In the cosmetics industry, 3-Hydroxycapric acid methyl ester is used as an ingredient in various skincare and hair care products due to its moisturizing and emollient properties. Its ability to form a protective barrier on the skin and hair helps retain moisture, providing a smooth and soft texture.
Used in Food Industry:
3-Hydroxycapric acid methyl ester is utilized as an additive in the food industry, where it serves as an emulsifier and stabilizer. Its ability to mix water and oil together helps create a uniform texture in various food products, enhancing their quality and shelf life.
Used in Research and Development:
As a colorless oil with unique chemical properties, 3-Hydroxycapric acid methyl ester is also used in research and development for the synthesis of new compounds and the study of their potential applications in various fields, including medicine, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 56618-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,1 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56618-58:
(7*5)+(6*6)+(5*6)+(4*1)+(3*8)+(2*5)+(1*8)=147
147 % 10 = 7
So 56618-58-7 is a valid CAS Registry Number.

56618-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (3R)-3-hydroxydecanoate

1.2 Other means of identification

Product number -
Other names D-3-Hydroxy-caprinsaeure-methylester

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:56618-58-7 SDS

56618-58-7Relevant articles and documents

(3S,8E)-1,3-Dihydroxy-8-decen-5-one, a Metabolite of Streptomyces fimbriatus

Keller-Schierlein, Walter,Wuthier, Damian,Drautz, Hannelore

, p. 1253 - 1261 (1983)

From the cultures of Streptomyces fimbriatus, strain Tue 2335, the title compound 1 was isolated by solvent extraction, chromatography, and distillation.Its constitution was determined by spectroscopic investigations of 1 and some of its derivatives, and the chirality by transformation to (R)-1,3-isopropylidenedioxydecane (12); a reference sample of the latter was prepared from (R)-methyl 3-hydroxydecanoate (10).In the equilibrium mixture the keto form 1 predominates the two hemiacetals 2a and 2b.Compound 1 is inactive against bacteria, yeasts and fungi.

Total Synthesis and Stereochemical Assignment of Sunshinamide and Its Anticancer Activity

Goswami, Rajib Kumar,Mondal, Joyanta,Sarkar, Ruma,Sen, Prosenjit

, (2020/02/15)

Total synthesis of cyclodepsipeptide sunshinamide has been achieved for the first time using a convergent approach. The key features of this synthesis comprise Crimmins acetate aldol, Shiina esterification, amide coupling, macrolactamization, and an Isub

Synthesis and Characterization of Four Diastereomers of Monorhamnolipids

Palos Pacheco, Ricardo,Eismin, Ryan J.,Coss, Clifford S.,Wang, Hui,Maier, Raina M.,Polt, Robin,Pemberton, Jeanne E.

, p. 5125 - 5132 (2017/05/04)

Rhamnolipids are amphiphilic glycolipids biosynthesized by bacteria that, due to their low toxicity and biodegradability, are potential replacements for synthetic surfactants. The previously limited access to pure materials at the gram scale has hindered

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