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19147-16-1

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19147-16-1 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 19147-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,4 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19147-16:
(7*1)+(6*9)+(5*1)+(4*4)+(3*7)+(2*1)+(1*6)=111
111 % 10 = 1
So 19147-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O4.K/c7-5(8)3-1-2-4-6(9)10;/h1-4H2,(H,7,8)(H,9,10);/q;+1

19147-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dipotassium,hexanedioate

1.2 Other means of identification

Product number -
Other names Adipicacid,dipotassium salt (8CI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives
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:19147-16-1 SDS

19147-16-1Relevant articles and documents

Oxidation studies of carbohydrates using molecular oxygen and a bismuth-ruthenium oxide catalyst

Arts, Stefan J.H.F.,Van Rantwijk, Fred,Sheldon, Roger A.

, p. 317 - 329 (1996)

The oxidation of trans-1,2-cyclohexanediol, methyl α-D-glucopyranoside and β-cyclodextrin has been studied, using a heterogeneous oxidation system in water at 50-75°C. Molecular oxygen at 15-20 bar was used as the oxidant, in combination with a bismuth-rich ruthenium pyrochlore oxide as the catalyst. Both oxidative cleavage of the vicinal diols and oxidation of the primary hydroxyl groups occurred. HPLC and 13C NMR were used to analyse the complex product mixtures. The oxidation method is successful for glycol cleavage in small carbohydrates but not for polysaccharides.

Optimization of a cyclohexanone distillation stage in the presence of alkali

Glazko,Levanova,Martynenko,Sokolova

experimental part, p. 1767 - 1771 (2012/02/05)

Kinetics of two reactions: hydrolysis of esters and condensation of cyclohexanone in an alkaline environment, was studied in model mixtures. Derived kinetic equations were used to assess optimal parameters of proceeding cyclohexanone distillation in the presence of alkali.

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