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1-Oleo-2-palmito-stearin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35984-52-2

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35984-52-2 Usage

Chemical composition

1-Oleo-2-palmito-stearin is a compound derived from a mixture of fatty acids, primarily containing oleic, palmitic, and stearic acids.

Natural occurrence

It is commonly found in natural fats and oils.

Industrial applications

Widely used in the production of various cosmetic and personal care products, as well as in the food industry.

Functional roles

Serves as an emulsifier and stabilizer in food products.

Suitability for emulsions

Has properties that make it suitable for use in emulsions.

Gelling properties

Acts as a gelling agent in formulations.

Pharmaceutical potential

Possesses therapeutic and medicinal properties that can be utilized in the development of new drugs and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 35984-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,8 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35984-52:
(7*3)+(6*5)+(5*9)+(4*8)+(3*4)+(2*5)+(1*2)=152
152 % 10 = 2
So 35984-52-2 is a valid CAS Registry Number.

35984-52-2Downstream Products

35984-52-2Relevant academic research and scientific papers

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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