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9,10-bis(acetoxy)octadecanoic acid is a chemical compound with the molecular formula C22H40O6. It is a derivative of octadecanoic acid, also known as stearic acid, which is a saturated fatty acid with an 18-carbon chain. The compound is characterized by the presence of two acetoxy groups attached to the 9th and 10th carbon atoms of the octadecanoic acid chain. This modification introduces two ester functional groups, which can be hydrolyzed to yield the parent carboxylic acid and acetic acid. 9,10-bis(acetoxy)octadecanoic acid is used in various applications, including the synthesis of surfactants, lubricants, and other industrial chemicals. Its properties, such as solubility and reactivity, can be tailored for specific uses through the acetoxy groups, making it a versatile intermediate in organic chemistry.

5929-62-4

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5929-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5929-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5929-62:
(6*5)+(5*9)+(4*2)+(3*9)+(2*6)+(1*2)=124
124 % 10 = 4
So 5929-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H40O6/c1-4-5-6-7-9-12-15-20(27-18(2)23)21(28-19(3)24)16-13-10-8-11-14-17-22(25)26/h20-21H,4-17H2,1-3H3,(H,25,26)

5929-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10-diacetyloxyoctadecanoic acid

1.2 Other means of identification

Product number -
Other names 9,10-diacetoxyoctadecanoic 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:5929-62-4 SDS

5929-62-4Downstream Products

5929-62-4Relevant academic research and scientific papers

Electroorganic synthesis 65. Anodic homocoupling of carboxylic acids derived from fatty acids

Weiper-Idelmann, Andreas,Aus Dem Kahmen, Martin,Schaefer, Hans J.,Gockeln, Marianne

, p. 672 - 682 (2007/10/03)

Fatty acid derived carboxylic acids with double bonds, hydroxy-, amino-, keto-, ester- and epoxy groups are anodically coupled to dimers (Kolbe electrolysis) in 29 to 81% yield and up to a 2.5 mol scale. Problems due to the low conductivity of fatty acid salts were overcome by the use of a flow cell with a narrow electrode gap. Fatty acids with branched alkyl chains gave dimers with interesting emulsifying properties. Dimethyl hexadecanedioate, accessible from methyl azelate, could be cyclized and further converted into homomuscone and muscone in a few steps. A commercial mixture of dimeric fatty acids (C36-dicarboxylic acids) has been coupled to give C70-diesters. Acta Chemica Scandinavica 1998. Part 64: Nielsen, M. F., Batanero, B.,.

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