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(24S)-ETHYLCHOLESTA-3,5,22-TRIENE is a cholesterol derivative and a member of the C27-steroids class of organic compounds. It is a sterol derivative, which is a type of lipid molecule that plays a vital role in maintaining the structure and function of cell membranes. This molecule is involved in essential biological processes such as hormone production, vitamin D synthesis, and bile acid formation. Its structure features a four-carbon aliphatic side chain, a double bond at the 5,6-position, and a 3-hydroxy group, making it an important molecule with various functions in the human body.

102491-96-3

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102491-96-3 Usage

Uses

Used in Pharmaceutical Industry:
(24S)-ETHYLCHOLESTA-3,5,22-TRIENE is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those related to cholesterol-lowering drugs and hormone therapies. Its role in hormone production and cholesterol regulation makes it a valuable component in the development of medications targeting these areas.
Used in Nutraceutical Industry:
(24S)-ETHYLCHOLESTA-3,5,22-TRIENE is used as a dietary supplement to support healthy cholesterol levels and promote overall cardiovascular health. Its involvement in cholesterol regulation and bile acid formation contributes to its use in nutraceutical products designed to maintain a balanced lipid profile.
Used in Cosmetic Industry:
(24S)-ETHYLCHOLESTA-3,5,22-TRIENE is used as an ingredient in cosmetic products, particularly those targeting skin health and anti-aging. Its role in maintaining cell membrane structure and function may contribute to the development of skincare products that promote healthy, youthful-looking skin.
Used in Research and Development:
(24S)-ETHYLCHOLESTA-3,5,22-TRIENE is used as a research compound in the study of cholesterol metabolism, hormone synthesis, and related biological processes. Its unique structure and function make it an important tool for understanding the complex interactions within the human body and developing new therapeutic approaches.

Check Digit Verification of cas no

The CAS Registry Mumber 102491-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102491-96:
(8*1)+(7*0)+(6*2)+(5*4)+(4*9)+(3*1)+(2*9)+(1*6)=103
103 % 10 = 3
So 102491-96-3 is a valid CAS Registry Number.

102491-96-3SDS

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 (24S)-ETHYLCHOLESTA-3,5,22-TRIENE

1.2 Other means of identification

Product number -
Other names stigmasta-3,5,22t-triene

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:102491-96-3 SDS

102491-96-3Downstream Products

102491-96-3Relevant academic research and scientific papers

Convenient synthesis of monomeric steroids from steroidal oxalate dimers using flash vacuum pyrolysis (FVP)

Nahar, Lutfun,Turner, Alan B.,Sarker, Satyajit D.

, p. 359 - 366 (2010)

Flash vacuum pyrolysis (FVP) or thermolysis (FVT), an environmentally friendly method for studying organic reaction mechanisms as well as synthesis, was applied to a series of oxalate dimers (1, 3, 5, 7, 9, 11, 13, and 15) to synthesise monomeric enes, dienes, and a triene (2, 4, 6, 8, 10, 12, 14, and 16). All steroidal monomers were identified by spectroscopic means. TUBITAK.

p-Toluenesulfonic Acid Adsorbed on Silica Gel: An Efficient Dehydrating Agent of Alcohols

D'Onofrio, Franco,Scettri, Arrigo

, p. 1159 - 1161 (2007/10/02)

Secondary and tertiary alcohols are efficiently dehydrated by reaction with p-toluenesulfonic acid supported on silica gel.In particular, the procedure allows the direct conversion of 3-hydroxy-steroids into Δ2-olefins or Δ3,5-dienes, without passing through the mesylate or tosylate esters.

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