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17598-92-4

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17598-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17598-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17598-92:
(7*1)+(6*7)+(5*5)+(4*9)+(3*8)+(2*9)+(1*2)=154
154 % 10 = 4
So 17598-92-4 is a valid CAS Registry Number.

17598-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name hexanoic acid 3-hexanoyloxy-2-hydroxypropyl ester

1.2 Other means of identification

Product number -
Other names 1,3-dihexanoylglycerol

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:17598-92-4 SDS

17598-92-4Downstream Products

17598-92-4Relevant articles and documents

Preparation of glycerol carbonate esters by using hybrid nafion-silica catalyst

Climent, Maria J.,Corma, Avelino,Iborra, Sara,Martinez-Silvestre, Sergio,Velty, Alexandra

, p. 1224 - 1234 (2013/07/26)

Glycerol carbonate esters (GCEs), which are valuable biomass-derivative compounds, have been prepared through the direct esterification of glycerol carbonate and long organic acids with different chain lengths, in the absence of solvent, and with heterogeneous catalysts, including acidic-organic resins, zeolites, and hybrid organic-inorganic acids. The best results, in terms of activity and selectivity towards GCEs, were obtained using a Nafion-silica composite. A full reaction scheme has been established, and it has been demonstrated that an undesired competing reaction results in the generation of glycerol and esters derived from a secondary hydrolysis of the endocyclic ester group, which is attributed to water formed during the esterification reaction. The influence of temperature, substrate ratio, catalyst-to-substrate ratio, and the use of solvent has been studied and, under optimized reaction conditions and with the adequate catalyst, it was possible to achieve 95 % selectivity for the desired product at 98 % conversion. It was demonstrated that the reaction rate decreased as the number of carbon atoms in the linear alkyl chain of the carboxylic acid increased for both p-toluenesulfonic acid and Nafion-silica nanocomposite (Nafion SAC-13) catalysts. After fitting the experimental data to a mechanistically based kinetic model, the reaction kinetic parameters for Nafion SAC-13 catalysis were determined and compared for reactions involving different carboxylic acids. A kinetic study showed that the reduced reactivity of carboxylic acids with increasing chain lengths could be explained by inductive as well as steric effects. Chain reaction: The esterification of glycerol carbonate with carboxylic acids to produce glycerol carbonate esters, which are valuable biomass-derivative compounds, has been investigated. A Nafion-silica nanocomposite is shown to be an excellent catalyst, and after fitting the experimental data to a kinetic model, the kinetic parameters were determined and compared for reactions involving different carboxylic acids. Copyright

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