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3-O-(1-hexadecyl)cholesterol is a derivative of cholesterol, a naturally occurring steroid found in the body. It is characterized by the presence of a 16-carbon (hexadecyl) alkyl chain attached to the 3-hydroxyl group of the cholesterol molecule. This modification enhances the solubility and stability of the compound in various environments, making it useful in pharmaceutical and cosmetic applications. The hexadecyl chain also influences the compound's interaction with cell membranes, potentially affecting membrane fluidity and function. Research on 3-O-(1-hexadecyl)cholesterol may provide insights into its role in modulating cellular processes and its potential therapeutic applications.

22032-48-0

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22032-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22032-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22032-48:
(7*2)+(6*2)+(5*0)+(4*3)+(3*2)+(2*4)+(1*8)=60
60 % 10 = 0
So 22032-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C43H78O/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-32-44-37-28-30-42(5)36(33-37)24-25-38-40-27-26-39(35(4)23-21-22-34(2)3)43(40,6)31-29-41(38)42/h24,34-35,37-41H,7-23,25-33H2,1-6H3/t35-,37+,38+,39-,40+,41+,42+,43-/m1/s1

22032-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,10R,13R,17R)-17-(1,5-Dimethyl-hexyl)-3-hexadecyloxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names -

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:22032-48-0 SDS

22032-48-0Downstream Products

22032-48-0Relevant academic research and scientific papers

The Synthesis of Cholesteryl Alkyl Ethers

Halperin, G.,Gatt, S.

, p. 39 - 42 (2007/10/02)

Seventeen cholesteryl alkyl ethers were synthesized through alcoholysis of cholesterol p-toluenesulfonate.This method was found superior to the etherification of sodium or potassium cholesterylate with alkyl halides or methanesulfonates, especially for the preparation of long-chain unsaturated alkyl ethers of cholesterol of high specific activity.

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