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bis(4-hydroxybutyl) adipate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20985-13-1

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20985-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20985-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,8 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20985-13:
(7*2)+(6*0)+(5*9)+(4*8)+(3*5)+(2*1)+(1*3)=111
111 % 10 = 1
So 20985-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O6/c15-9-3-5-11-19-13(17)7-1-2-8-14(18)20-12-6-4-10-16/h15-16H,1-12H2

20985-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-hydroxybutyl) hexanedioate

1.2 Other means of identification

Product number -
Other names EINECS 244-138-1

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:20985-13-1 SDS

20985-13-1Downstream Products

20985-13-1Relevant academic research and scientific papers

Mechanistic studies on the enzymatic transesterification of polyesters

McCabe,Taylor

, p. 765 - 770 (2004)

The effect of solvents on the enzymatic transesterification of aliphatic polyesters has been investigated. It has been shown that the hydrophobicity and the polarity of the solvent have little effect on the reaction, however, the molecular weight of the product depends on the solubility of the product in the medium. Above a certain molecular weight, when the product is no longer soluble in the medium, transesterification does not occur. Deuterium NMR studies have shown that transesterification tends to take place at the ends of the polymer chain rather than at random along the polymer chain.

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