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Cholesteryl caprylate, a derivative of cholesterol (C432501), is a white fine crystalline powder. Cholesterol is a vital component of all biological membranes, making up approximately 25% of the total brain lipid content. It is the principal sterol found in higher animals and is present in all body tissues, particularly in the brain, spinal cord, and animal fats or oils. Cholesterol is also the main constituent of gallstones.

1182-42-9

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1182-42-9 Usage

Uses

Used in Pharmaceutical Industry:
Cholesteryl caprylate is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its cholesterol-based structure allows for easy integration into drug formulations targeting specific biological pathways.
Used in Cosmetics Industry:
Cholesteryl caprylate is used as an emollient and skin conditioning agent for [application reason]. Its ability to penetrate the skin and improve its softness and smoothness makes it a valuable ingredient in cosmetic products.
Used in Food Industry:
Cholesteryl caprylate is used as a fat substitute or fortifier for [application reason]. Its cholesterol-like properties enable it to mimic the texture and mouthfeel of fats, making it suitable for low-fat or fat-free food products.
Used in Research Applications:
Cholesteryl caprylate is used as a research tool for [application reason]. Its unique chemical properties make it useful in studying the role of cholesterol in various biological processes and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1182-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1182-42:
(6*1)+(5*1)+(4*8)+(3*2)+(2*4)+(1*2)=59
59 % 10 = 9
So 1182-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C35H60O2/c1-7-8-9-10-11-15-33(36)37-28-20-22-34(5)27(24-28)16-17-29-31-19-18-30(26(4)14-12-13-25(2)3)35(31,6)23-21-32(29)34/h16,25-26,28-32H,7-15,17-24H2,1-6H3/t26-,28+,29+,30-,31+,32+,34+,35-/m1/s1

1182-42-9 Well-known Company Product Price

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  • (1132001)  Cholesterylcaprylate  United States Pharmacopeia (USP) Reference Standard

  • 1182-42-9

  • 1132001-200MG

  • 4,662.45CNY

  • Detail

1182-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octanoate

1.2 Other means of identification

Product number -
Other names 3beta-Hydroxy-5-cholestene 3-octanoate

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:1182-42-9 SDS

1182-42-9Downstream Products

1182-42-9Relevant academic research and scientific papers

FeCl3·6H2O as a versatile catalyst for the esterification of steroid alcohols with fatty acids

Komura, Kenichi,Ozaki, Akiyoshi,Ieda, Noboru,Sugi, Yoshihiro

, p. 3407 - 3410 (2008)

FeCl3·6H2O is an active catalyst for the esterification of some steroid alcohols with fatty acids under azeotropic reflux in mesitylene as solvent. Georg Thieme Verlag Stuttgart.

Microbial Transformation on Interface between Hydrophilic Carriers and Hydrophobic Organic Solvents

Oda, Shinobu,Ohta, Hiromichi

, p. 2041 - 2045 (2007/10/02)

A new method for the microbial transformation of water-insoluble compounds is proposed.Microorganisms were placed on the interface between hydrophilic carriers such as agar and hydrophobic organic solvents.These microorganisms could catalyze various transformations of synthetic substrates such as hydrolysis, esterification, oxidation, and reduction more efficiently than emulsion systems.This new type of bioreactor was tentatively named as Interface Bioreactor.

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