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26719-47-1

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26719-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26719-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26719-47:
(7*2)+(6*6)+(5*7)+(4*1)+(3*9)+(2*4)+(1*7)=131
131 % 10 = 1
So 26719-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C38H74O4/c1-3-5-7-9-11-13-15-17-19-23-27-31-35-41-37(39)33-29-25-21-22-26-30-34-38(40)42-36-32-28-24-20-18-16-14-12-10-8-6-4-2/h3-36H2,1-2H3

26719-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ditetradecyl decanedioate

1.2 Other means of identification

Product number -
Other names Decandisaeure-ditetradecylester

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:26719-47-1 SDS

26719-47-1Downstream Products

26719-47-1Relevant articles and documents

Sustainable process for the production of symmetrical dibasic acid ester-based thermal energy storage materials from lipids

Yildirim, Ayhan,Kiraylar, Kaan

, p. 802 - 808 (2019/07/17)

Oleochemical-based long-chain diesters are potential organic phase change materials convenient for thermal energy storage. The development of efficient and green methods is an important requirement for the preparation of these environmentally friendly compounds, which also are finding wide industrial application. Thus, in the present work, a series of dibasic acid esters were synthesized through ionic liquid catalyzed scalable chemical esterification or transesterification reactions in a solvent-free medium. The starting compounds, dicarboxylic acids or their methyl esters and fatty alcohols or cholesterol, were reacted in the ratio of 1:2 respectively and the synthesized esters were characterized by FT-IR, 1 H NMR, and 13 C NMR.

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