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Alpha-Spinasterol acetate, a naturally occurring chemical compound found in various plant sources such as spinach, is classified as a sterol ester, a type of lipid present in plants, animals, and fungi. It has demonstrated potential pharmacological and biological activities, including anti-inflammatory, anti-microbial, and anti-oxidant properties. With its therapeutic potential in treating various diseases like cancer and cardiovascular conditions, alpha-Spinasterol acetate is a promising compound for further exploration and development in the fields of medicine and biochemistry.

4651-46-1

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4651-46-1 Usage

Uses

Used in Pharmaceutical Industry:
Alpha-Spinasterol acetate is used as a therapeutic agent for its anti-inflammatory, anti-microbial, and anti-oxidant properties, which contribute to the treatment of various diseases, including cancer and cardiovascular conditions.
Used in Nutraceutical Industry:
Alpha-Spinasterol acetate is used as a dietary supplement for its health-promoting properties, such as reducing inflammation and supporting cardiovascular health.
Used in Cosmetic Industry:
Alpha-Spinasterol acetate is used as an ingredient in skincare products for its anti-oxidant and anti-inflammatory properties, which can help protect the skin from environmental damage and promote a healthy complexion.
Used in Agricultural Industry:
Alpha-Spinasterol acetate is used as a natural pesticide or fungicide due to its anti-microbial properties, helping to protect crops from diseases and pests.
Used in Food Industry:
Alpha-Spinasterol acetate is used as a natural preservative in food products to extend shelf life and maintain freshness, as well as for its potential health benefits when consumed.

Check Digit Verification of cas no

The CAS Registry Mumber 4651-46-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4651-46:
(6*4)+(5*6)+(4*5)+(3*1)+(2*4)+(1*6)=91
91 % 10 = 1
So 4651-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C31H50O2/c1-8-23(20(2)3)10-9-21(4)27-13-14-28-26-12-11-24-19-25(33-22(5)32)15-17-30(24,6)29(26)16-18-31(27,28)7/h9-10,12,20-21,23-25,27-29H,8,11,13-19H2,1-7H3/b10-9+/t21-,23-,24+,25+,27-,28+,29+,30+,31-/m1/s1

4651-46-1SDS

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 (3β,5α,22E)-Stigmasta-7,22-dien-3-yl acetate

1.2 Other means of identification

Product number -
Other names spinasteryl acetate

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:4651-46-1 SDS

4651-46-1Relevant academic research and scientific papers

A 24β-ETHYL-Δ7-STERYL GLUCOPYRANOSIDE FROM CUCURBITA PEPO SEEDS

Rauwald, Hans-Willi,Sauter, Michael,Schilcher, Heinz

, p. 2746 - 2748 (1985)

In the seeds of Cucurbita pepo three closely related 24-ethyl-Δ7-steryl glucosides were identified by hydrolytic studies and spectral analysis as spinasteryl-β-D-glucopyranoside, the new 3-O-(β-D-glucopyranosyl)-24β-ethyl-5α-cholesta-7,25(27)-dien-3β-ol and the corresponding Δ22E,25(27)-trienol.Except for its occurence in cucumber seeds the latter is so far unknown as a natural product. Key Word Index - Cucurbita pepo; Cucurbitaceae; pumpkin; seeds; steryl glucosides; 3-O-(β-D-glucopyranosyl)-24β-ethyl-5α-cholesta-7,25(27)dien-3-β-ol; 3-O-(β-D-glucopyranosyl) -24β-ethyl-5α-cholesta-7,trans-22,25(27)-trien-3β-ol; spinasteryl-β-D-glucopyranoside.

Synthesis of Chondrillasterol and Spinasterol

Anastasia, Mario,Fiecchi, Alberto,Scala, Antonio,Puppo, Marina del

, p. 2561 - 2562 (2007/10/02)

Spinasterol (1a) and chondrillasterol (1b) have been synthesized from the ethyl (22E,24S)-and (22E,24R)-3β-acetoxy-5α-stigmasta-7,22-dien-29-oates, (2c) and (2d), respectively.

Constituents of Albizzia zygia

Schoppa, Thomas,Pachaly, Peter

, p. 18 - 25 (2007/10/02)

Lupen-20(30)-3β-ol (1), 14α-stigmast-5-en-3β-ol (3) and 5α-stigmast-7,22-dien-3β-ol (5) were isolated from the bark of Albizzia zygia (Mimosaceae).Leaves also contain these substances and, in addition, a glycoside of 1 as well as four further compounds which give a positive reaction with SbCl3.

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