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9-Hydroxystearic acid methyl ester, also known as methyl 9-hydroxystearate, is a chemical compound with the molecular formula C19H38O3. It is a derivative of 9-hydroxystearic acid, where the carboxylic acid group is esterified with methanol, resulting in a methyl ester. This organic compound is a white, waxy solid that is insoluble in water but soluble in organic solvents. It is commonly used in the production of lubricants, plasticizers, and as an intermediate in the synthesis of various chemicals. The compound is also known for its potential applications in the pharmaceutical and cosmetic industries due to its emollient properties.

2447-53-2

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2447-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2447-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2447-53:
(6*2)+(5*4)+(4*4)+(3*7)+(2*5)+(1*3)=82
82 % 10 = 2
So 2447-53-2 is a valid CAS Registry Number.

2447-53-2SDS

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 9-hydroxyoctadecanoate

1.2 Other means of identification

Product number -
Other names 9-hydroxyoctadecanoic acid methyl ester

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:2447-53-2 SDS

2447-53-2Relevant academic research and scientific papers

Synthesis, Characterisation, and Transformations of a Lipid Cyclic Peroxide

Bascetta, Emanuele,Gunstone, Frank D.,Scrimgeour, Charles M. S.

, p. 2199 - 2206 (2007/10/02)

Photosensitised oxidation of (9E,11E)-methyl octadeca-9,11-dienoate gave an unsaturated cyclic peroxide (epidioxide) in high yield.This was characterised spectroscopically.The peroxide underwent facile rearrangement to a furanoid ester under a variety of reaction conditions.Catalytic reduction of the unsaturated peroxide cleaved the O-O bond.Bromination and epoxidation gave dibromo and epoxy esters respectively with the peroxide group still intact.

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