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7-Hydroxyoctadecanoic acid methyl ester is a chemical compound with the molecular formula C19H38O3. It is a derivative of 7-hydroxyoctadecanoic acid, where a methyl group (CH3) is attached to the hydroxyl group (OH) through an ester linkage. 7-Hydroxyoctadecanoic acid methyl ester is a fatty acid ester, specifically a long-chain fatty acid with a hydroxyl group at the 7th carbon position. It is known for its potential applications in the pharmaceutical and cosmetic industries, where it may be used as an emollient or moisturizing agent due to its ability to form a barrier on the skin and retain moisture. The esterification process enhances its solubility in oils and organic solvents, which can be beneficial for formulation in various products.

2379-96-6

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2379-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2379-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2379-96:
(6*2)+(5*3)+(4*7)+(3*9)+(2*9)+(1*6)=106
106 % 10 = 6
So 2379-96-6 is a valid CAS Registry Number.

2379-96-6SDS

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 methyl 7-hydroxyoctadecanoate

1.2 Other means of identification

Product number -
Other names 7-Hydroxy-octadecansaeure-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:2379-96-6 SDS

2379-96-6Downstream Products

2379-96-6Relevant academic research and scientific papers

Enzymatic kinetic resolution of hydroxystearic acids: A combined experimental and molecular modelling investigation

Ebert, Cynthia,Felluga, Fulvia,Forzato, Cristina,Foscato, Marco,Gardossi, Lucia,Nitti, Patrizia,Pitacco, Giuliana,Boga, Carla,Caruana, Paolo,Micheletti, Gabriele,Calonghi, Natalia,Masotti, Lanfranco

, p. 38 - 45 (2012)

Enantioenriched 7-, 8-, 9-, and 10-hydroxystearic acids (HSA) were obtained, for the first time, by kinetic resolution of their racemates with lipases CALB and PS, in the presence of vinyl acetate. Among them, the best results were obtained for 7-HSA and 9-HSA, whose enantiomeric excess was around 55%. The same resolutions carried out on the hydroxy esters completely failed. For the acid substrates neither the Kazlauskas' rule nor the 3D-QSAR model could be applied, since both models are focused on the CALB alcohol-pocket evaluation and not on the acyl-pocket one. Therefore, a semiquantitative approach was used, whose results were in accordance with our findings, as far as the absolute configuration of the product is concerned.

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