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Cholestan-3-ol, 4-methyl-, (3beta,4alpha,5alpha)-, also known as 4-methylcholestanol or 4-methyl-5alpha-cholestan-3-ol, is a naturally occurring steroid alcohol derived from cholesterol. It is characterized by the presence of a methyl group at the 4th carbon position and a hydroxyl group at the 3rd carbon position. Cholestan-3-ol, 4-methyl-, (3beta,4alpha,5alpha)- is an important intermediate in the biosynthesis of various steroid hormones and plays a crucial role in the metabolism of cholesterol. 4-methylcholestanol is found in various biological samples, including human plasma, and has been used as a biomarker for the assessment of cholesterol metabolism and the diagnosis of certain diseases. Its chemical structure and biological significance make it an essential component in the study of steroid chemistry and endocrinology.

3903-57-9

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3903-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3903-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3903-57:
(6*3)+(5*9)+(4*0)+(3*3)+(2*5)+(1*7)=89
89 % 10 = 9
So 3903-57-9 is a valid CAS Registry Number.

3903-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4α-methyl-5α-cholestan-3β-ol

1.2 Other means of identification

Product number -
Other names 4α-Methyl-5α-cholestanol-(3β)

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:3903-57-9 SDS

3903-57-9Relevant academic research and scientific papers

Regio- and stereospecific synthesis of cholesterol derivatives and their hormonal activity in Caenorhabditis elegans

Schmidt, Arndt W.,Doert, Thomas,Goutal, Sigrid,Gruner, Margit,Mende, Fanny,Kurzchalia, Teymuras V.,Knoelker, Hans-Joachim

, p. 3687 - 3706 (2007/10/03)

Cholesterol is essential for the survival of the nematode Caenorhabditis elegans. Recent studies have demonstrated that cholesterol derivatives regulate two processes in the life cycle of worms: controlling molting and inducing a specialized non-feeding larval stage. However, the chemical structure of the cholesterol-derived signalling molecules for these or any other functions has not yet been identified. Herein, we describe the regio- and stereospecific synthesis of a number of cholesterol derivatives. The lithium-ammonia reduction of 4-cholesten-3-one was utilized to develop a general method for the introduction of diverse functional groups at C-4α of 5α-cholestan- 3β-ol. Stereoselective functionalization at C-7 was achieved starting from 7-ketocholesterol derivatives. 6-Keto-5α-cholestan-3β-ol was utilized for specific functionalizations at C-6 and C-7. The structure-activity relationships of the different cholesterol derivatives have been investigated by feeding worms of different genetic background with these compounds. Our study is the first step in assigning the relationships of hormonal activity in C. elegans on the substitution at different positions of cholesterol. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

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