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Cholest-5-ene-3,7,22-triol, also known as an oxysterol, is a cholesterol derivative that has hydroxy groups at positions 7alpha and 22R. It is a naturally occurring compound found in small amounts in various biological systems, including human plasma and tissues.

104786-66-5

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104786-66-5 Usage

Uses

Used in Pharmaceutical Industry:
Cholest-5-ene-3,7,22-triol is used as a pharmaceutical agent for its potential therapeutic effects on various health conditions. It has been found to possess anti-inflammatory, anti-atherogenic, and neuroprotective properties, making it a promising candidate for the treatment of inflammatory diseases, cardiovascular disorders, and neurodegenerative diseases.
Used in Research Applications:
Cholest-5-ene-3,7,22-triol is used as a research tool in the study of cholesterol metabolism and its role in various physiological and pathological processes. It helps researchers understand the mechanisms of cholesterol transport, regulation, and its impact on cellular functions.
Used in Cosmetic Industry:
Cholest-5-ene-3,7,22-triol is used as an ingredient in cosmetic products for its potential benefits to skin health. It is believed to have moisturizing, anti-aging, and skin-regenerating properties, making it a valuable component in skincare formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 104786-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,8 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104786-66:
(8*1)+(7*0)+(6*4)+(5*7)+(4*8)+(3*6)+(2*6)+(1*6)=135
135 % 10 = 5
So 104786-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C27H46O3/c1-16(2)6-9-23(29)17(3)20-7-8-21-25-22(11-13-27(20,21)5)26(4)12-10-19(28)14-18(26)15-24(25)30/h15-17,19-25,28-30H,6-14H2,1-5H3/t17-,19-,20+,21-,22-,23+,24+,25-,26-,27+/m0/s1

104786-66-5SDS

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 (7α,22R)-dihydroxycholesterol

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:104786-66-5 SDS

104786-66-5Downstream Products

104786-66-5Relevant academic research and scientific papers

Stereospecific Syntheses of the Four Epimers of 7,22-Dihydroxycholesterol

Amann, Alain,Ourisson, Guy,Luu, Bang

, p. 1002 - 1005 (1987)

Four stereospecific pathways are presented yielding each of the four epimers of 7,22-dihydroxycholesterol from aldehyde 1, in over 50percent yield.

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