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7alpha-Hydroxystigmasterol is a plant-derived sterol compound and a member of the phytosterol group, which are structurally similar to cholesterol and are integral components of plant cell membranes. 7alpha-Hydroxystigmasterol has garnered attention for its potential health benefits, such as its anti-inflammatory and antioxidant properties, as well as its cholesterol-lowering effects that could contribute to cardiovascular health. Furthermore, 7alpha-Hydroxystigmasterol has demonstrated neuroprotective potential, suggesting its ability to safeguard brain cells and possibly mitigate the risk of cognitive decline. As a result, 7alpha-Hydroxystigmasterol is a compound of significant interest with promising health benefits that are currently under investigation for various medical applications.

64998-19-2

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64998-19-2 Usage

Uses

Used in Cardiovascular Health Applications:
7alpha-Hydroxystigmasterol is used as a cholesterol-lowering agent for promoting cardiovascular health. Its ability to interfere with cholesterol absorption in the intestines can help reduce blood cholesterol levels, thereby potentially lowering the risk of heart disease.
Used in Anti-Inflammatory Applications:
As an anti-inflammatory agent, 7alpha-Hydroxystigmasterol is utilized to reduce inflammation in the body. Its anti-inflammatory properties can be beneficial in managing conditions characterized by excessive inflammation.
Used in Antioxidant Applications:
7alpha-Hydroxystigmasterol serves as an antioxidant, protecting cells from oxidative stress and damage caused by free radicals. This function can contribute to overall health and the prevention of various diseases associated with oxidative stress.
Used in Neuroprotective Applications:
7alpha-Hydroxystigmasterol is used as a neuroprotective agent to shield brain cells from damage and degeneration. Research indicates its potential to reduce the risk of cognitive decline and protect against neurodegenerative diseases.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 7alpha-Hydroxystigmasterol is used as an active pharmaceutical ingredient for developing medications targeting a range of health conditions, from cardiovascular diseases to neurodegenerative disorders, capitalizing on its multifaceted health benefits.
Used in Nutraceutical Industry:
7alpha-Hydroxystigmasterol is used as a nutraceutical ingredient in dietary supplements and functional foods, aiming to provide consumers with the health benefits associated with this sterol compound, such as supporting cognitive function and cardiovascular health.

Check Digit Verification of cas no

The CAS Registry Mumber 64998-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,9 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64998-19:
(7*6)+(6*4)+(5*9)+(4*9)+(3*8)+(2*1)+(1*9)=182
182 % 10 = 2
So 64998-19-2 is a valid CAS Registry Number.

64998-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3β,7α,22E)-Stigmasta-5,22-diene-3,7-diol

1.2 Other means of identification

Product number -
Other names cholest-5-en-3beta,24S-diol

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:64998-19-2 SDS

64998-19-2Downstream Products

64998-19-2Relevant academic research and scientific papers

Mass spectrometry characterization of the 5α-, 7α-, and 7β-hydroxy derivatives of β-sitosterol, campesterol, stigmasterol, and brassicasterol

Bortolomeazzi, Renzo,De Zan, Michela,Pizzale, Lorena,Conte, Lanfranco S.

, p. 3069 - 3074 (2007/10/03)

The 5α-hydroperoxides of β-sitosterol, campesterol, stigmasterol, and brassicasterol were obtained by photooxidation of the respective sterols in pyridine in the presence of hematoporphyrine as sensitizer. The reduction of the hydroperoxides gives the corresponding 5α-hydroxy derivatives. The 7α- and 7β-hydroperoxides of the sterols were obtained by allowing an aliquot of the 5α-hydroperoxides to isomerize to 7α-hydroperoxides, which in turn epimerize to 7β-hydroperoxides. The reduction gave the corresponding 7α- and 7β-hydroxy derivatives. The 5α-, 7α-, and 7β-hydroxy derivatives of β-sitosterol, campesterol, stigmasterol, and brassicasterol were identified by comparing thin-layer chromatography mobilities, specific color reactions, and mass spectral data with those of the corresponding hydroxy derivatives of cholesterol, which were synthesized in the same manner. The phytosterols had the same behavior to photooxidation as cholesterol and, moreover, the different phytosterols photooxidized at about the same rate. The mass spectra of the trimethylsilyl ethers of the hydroxy derivatives of the phytosterols investigated and of the corresponding hydroxy derivatives of cholesterol have the same fragmentation patterns and similar relative ion abundances.

Synthesis of 7-oxo- and 7-hydroxy-derivatives of stigmasterol

Kovganko, N. V.,Chernov, Yu. G.

, p. 183 - 186 (2007/10/03)

The phytosteroids 3β-hydroxy-(24S)-stigmast-5,22E-dien-7-one and (24S)-stigmasta-5,22E-diene-3β,7β-diol have been synthesized from stigmasterol.

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