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7460-84-6

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7460-84-6 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 7460-84-6 differently. You can refer to the following data:
1. Labelled Glycidyl Stearate tance
2. Glycidyl Stearate is an acid-hydrolyzable ester derivatives as low calorie fat mimetics. It is used in frying oil, margarine, ice cream, milk substitutes and bakery. Carcinogenic substance.
3. Acid-hydrolyzable ester derivatives as low calorie fat mimetics

Check Digit Verification of cas no

The CAS Registry Mumber 7460-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7460-84:
(6*7)+(5*4)+(4*6)+(3*0)+(2*8)+(1*4)=106
106 % 10 = 6
So 7460-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H40O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(22)24-19-20-18-23-20/h20H,2-19H2,1H3

7460-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Glycidyl Stearate

1.2 Other means of identification

Product number -
Other names oxiran-2-ylmethyl octadecanoate

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:7460-84-6 SDS

7460-84-6Downstream Products

7460-84-6Relevant articles and documents

Synthesis of Triglycerides from 1,3-Dibromopropan-2-ol

Bhati, Asharam,Hamilton, Richard J.,Steven, David A.,Aneja, Rajender,Padley, Frederick B.

, p. 1553 - 1558 (2007/10/02)

1,3-Dibromopropan-2-ol (I) was converted into an acyl derivative (VI) by reaction with an appropriate acyl chloride in the presence of pyridine.The acyl derivative (VI) was subjected to nucleophilic substitution with 3 mol. equiv. tris(decyl)methylammonium carboxylate in refluxing hexane.This led to symmetrical diacid triglycerides in 90-94percent yield.Substitution with an equimolar amount of the carboxylate afforded, predominantly, the 1,2-bisacyloxy-3-bromopropane (VII) which could be easily isolated and further substituted to give unsymmetrical diacid- and triacid-triglycerides in ca. 96percent yield.Lipolysis showed the synthetic triglycerides to be ca. 99percent pure.

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