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Nonanedioic acid, monobutyl ester, also known as Azelaic acid monobutyl ester or Nonanedioic acid, butyl ester, is a chemical compound with the molecular formula C13H24O4. It is an ester derived from nonanedioic acid (azelaic acid) and butanol. This organic compound is characterized by its long-chain structure, consisting of a nine-carbon dicarboxylic acid and a four-carbon alcohol. Nonanedioic acid, monobutyl ester is used in various applications, including as a plasticizer, a lubricant, and a component in the production of certain polymers. It is also found in some personal care products and pharmaceuticals due to its potential skin-lightening properties, as it is structurally similar to the natural skin lightening agent, kojic acid.

4753-32-6

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4753-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4753-32-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4753-32:
(6*4)+(5*7)+(4*5)+(3*3)+(2*3)+(1*2)=96
96 % 10 = 6
So 4753-32-6 is a valid CAS Registry Number.

4753-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-butoxy-9-oxononanoic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4753-32-6 SDS

4753-32-6Relevant academic research and scientific papers

SELECTIVE MONOETHERIFICATION AND MONOESTERIFICATION OF DIOLS AND DIACIDS UNDER PHASE-TRANSFER CONDITIONS

Zerda, Jaime de la,Barak, Gabriela,Sasson, Yoel

, p. 1533 - 1536 (2007/10/02)

Research on the selectivity of etherification reactions of diols and esterification reactions of diacids by alkyl halides under phase-transfer catalysis has shown that under such conditions, selectivity of monoetherification increases in the order prim sec tert diols, though overall yield of monoether decreases from sec to tert diols.Monoesterification of diacids was accomplished with a high degree of selectivity.Optimal extraction of diols and diacids was found to correspond in general to chain lengths of around 5 carbons.This could mean that the complex formed between the catalyst and the anion to react is stabilized for certain carbon lengths by inner solvation in virtue of its spatial conformation.

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