7460-84-6 Usage
Description
Stearic Acid Glycidyl Ester, also known as Labelled Glycidyl Stearate, is an acid-hydrolyzable ester derivative that serves as a low-calorie fat mimetic. It is a versatile compound with various applications across different industries due to its unique properties.
Uses
Used in Food Industry:
Stearic Acid Glycidyl Ester is used as a low-calorie fat mimetic for providing a healthier alternative to traditional fats. It is used in frying oil, margarine, ice cream, milk substitutes, and bakery products to reduce calorie content while maintaining the desired texture and taste.
Used in Cosmetics and Personal Care Industry:
Stearic Acid Glycidyl Ester is used as an emulsifier and thickener in various cosmetic and personal care products, such as creams, lotions, and shampoos. Its ability to create stable emulsions and improve the texture of these products makes it a valuable ingredient in the formulation of these products.
However, it is important to note that Stearic Acid Glycidyl Ester is considered a carcinogenic substance, which may raise concerns regarding its safety for use in certain applications. Further research and regulations may be necessary to ensure its safe use in various industries.
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
7460-84-6Relevant 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.
