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19670-49-6

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19670-49-6 Usage

Chemical Properties

Colourless or slightly yellow, oily liquid or soft mass

Uses

1-Octanoyl-rac-glycerol (cas# 19670-49-6) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 19670-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19670-49:
(7*1)+(6*9)+(5*6)+(4*7)+(3*0)+(2*4)+(1*9)=136
136 % 10 = 6
So 19670-49-6 is a valid CAS Registry Number.

19670-49-6SDS

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 MONOCAPRYLIN

1.2 Other means of identification

Product number -
Other names OCTANOIN

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:19670-49-6 SDS

19670-49-6Related news

Vapour liquid equilibria of MONOCAPRYLIN (cas 19670-49-6) plus palmitic acid or methyl stearate at P = (1.20 and 2.50) kPa by using DSC technique07/14/2019

The Differential Scanning Calorimetry (DSC) technique is used for measuring isobaric (vapour + liquid) equilibria for two binary mixtures: {monocaprylin + palmitic acid (system 1) or methyl stearate (system 2)} at two different pressures P = (1.20 and 2.50) kPa. The obtained PTx data are correla...detailed

Antibacterial Effect of Caprylic Acid and MONOCAPRYLIN (cas 19670-49-6) on Major Bacterial Mastitis Pathogens07/13/2019

Bovine mastitis is the most significant economic drain on the worldwide dairy industry. Concerns regarding poor cure rates, emergence of bacterial resistance, and residues in milk necessitate development of alternative therapeutic approaches to antibiotics for treatment of mastitis. A variety of...detailed

19670-49-6Relevant articles and documents

Schoenheyder,Volqvartz

, p. 147,148 (1950)

METHOD FOR PREPARING MONOGLYCERIDES

-

Paragraph 0079-0081; 0084; 0085, (2020/08/18)

The present application relates to a method for preparing monoglycerides, a method for recovering glycerin and catalysts after the process for preparing monoglycerides, and a process for preparing cyclic monoglycerides.(AA) Fatty acid glycerin catalyst(BB) Esterification(CC) Reuse(DD) Settling and separation(EE) Glycerin and most of catalyst(F1,F2) Glyceride layer(GG) Glycerin(HH) Washing and separation(II) Glycerin and traces of catalyst(JJ) Glyceride layer(KK) Molecular distillation(LL) Glycerin and unreacted fatty acid(MM) Di- and tri-glycerideCOPYRIGHT KIPO 2020

Biobased catalyst in biorefinery processes: Sulphonated hydrothermal carbon for glycerol esterification

De La Calle, Carlos,Fraile, José M.,García-Bordejé, Enrique,Pires, Elísabet,Roldán, Laura

, p. 2897 - 2903 (2015/05/13)

Sulphonated hydrothermal carbon (SHTC), obtained from d-glucose by mild hydrothermal carbonisation and subsequent sulphonation with sulphuric acid, is able to catalyse the esterification of glycerol with different carboxylic acids, namely, acetic, butyric and caprylic acids. Product selectivity can be tuned by simply controlling the reaction conditions. On the one hand, SHTC provides one of the best selectivity towards monoacetins described up to now without the need for an excess of glycerol. On the other hand, excellent selectivity towards triacylglycerides (TAG) can be obtained, beyond those described with other solid catalysts, including well-known sulphonic resins. Recovery of the catalyst showed partial deactivation of the solid. The formation of sulphonate esters on the surface, confirmed by solid state NMR, was the cause of this behaviour. Acid treatment of the used catalyst, with subsequent hydrolysis of the surface sulphonate esters, allows SHTC to recover its activity. The higher selectivity towards mono- and triesters and its renewable origin makes SHTC an attractive catalyst in biorefinery processes.

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