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Stigmasterol

  • CasNo.:83-48-7
  • Purity:
  • Content:
  • MF:C29H48O
  • Packing:
  • MW:412.7
  • Apply:
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Factory supply good quality Stigmasterol 83-48-7 with stock

  • Molecular Formula:C29H48O
  • Molecular Weight:412.7
  • Appearance/Colour:White solid 
  • Vapor Pressure:9.21E-10mmHg at 25°C 
  • Melting Point:161-170 °C 
  • Refractive Index:1.504 
  • Boiling Point:501.1 °C at 760 mmHg 
  • PKA:15.03±0.70(Predicted) 
  • Flash Point:219.4 °C 
  • PSA:20.23000 
  • Density:0.98 g/cm3 
  • LogP:7.80080 

Stigmasterol(Cas 83-48-7) Usage

Biochem/physiol Actions

Stigmasterol possesses anti-inflammatory anti-hypercholestrolemic, antitumor and antioxidant functionality. It plays a crucial role in the activation of plasma membrane H+-ATPase and cell proliferation. Variations in stigmasterol and its precursor are noticeable at both the seed and whole plant developmental stages. Stigmasterol may be involved in gravitropism and tolerance to abiotic stress.

Purification Methods

Stigmasterol is best purified via the tetrabromide-acetate. The impure sterol (3g) is acetylated with Ac2O (60mL) by refluxing for 1.5hour. The mixture is cooled at 20o for 1hour, and the crude acetate is collected. The acetate (3g) in Et2O (30mL) is then treated with Br2/AcOH (38mL, from 5g Br2 in 100mL AcOH), and after cooling at 6o overnight, the tetrabromoacetate is filtered off and washed with Et2O. After six recrystallisations from CHCl3/MeOH the tetrabromoacetate has m 194-196o. This product (1g) in AcOH (12mL) and Zn dust (1g) is refluxed for 1.5hours, filtered hot, diluted with H2O (30mL) and extracted with Et2O. The extract is washed with dilute aqueous sodium sulfite, then H2O, the extract is dried (Na2SO4) and the stigmasterol acetate (~550mg) is recrystallised (4x) from EtOH and twice from MeOH/CHCl3 (2:1) to give the acetate with m 139-148o. This acetate (400mg) is hydrolysed in boiling 10% alcoholic KOH (1mL) for 1hour. Then H2O (30mL) is added and the mixture is extracted with Et2O. The extract is washed with aqueous Na2CO3, then H2O, the solvent is distilled off and the residue is recrystallised (3x) from 95% EtOH to give ~110mg of pure stigmasterol. It is dried in a vacuum over P2O5 for 3hours at 90o. The purity is checked by NMR. The acetate crystallises from MeOH with m 145o, [] D 25 -56o (c 2, CHCl3). [Byerrum & Ball Biochemical Preparations 7 86 1959, Thornton et al. J Am Chem Soc 62 2006 1940, Colin et al. Anal Chem 51 1661 1979, Beilstein 6 IV 4170.]

Definition

ChEBI: A 3beta-sterol that consists of 3beta-hydroxystigmastane having double bonds at the 5,6- and 22,23-positions.

General Description

Stigmasterol is a plant sterol that comprises an unsaturated bond between C22 and C23. It is found in foods like margarines and yogurts. Stigmasterol is synthesized from the mevalonate pathway and is present during development stages in plants.

InChI:InChI=1/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-9,19-22,24-27H,7,10-18H2,1-6H3/b9-8+/t20-,21-,22-,24+,25-,26+,27+,28+,29-/m1/s1

83-48-7 Relevant articles

NOVEL METHOD FOR SYNTHESIZING 25-OH CHOLESTEROL/CALCIFEDIOL FROM PHYTOSTEROL

-

Page/Page column 18-19, (2020/11/23)

The present invention discloses novel me...

Stigmasteryl arachidate constituent from the straw of oryza sativa

Chung, Ill-Min,Yoon, Jae-Yeon,Kim, Seung-Hyun,Ahmad, Ateeque

, p. 3018 - 3020 (2014/06/09)

One compound stigmasteryl-3β-arachidate ...

Stigmasterol-3-O-β-D-arabinopyranosyl(1→4)-O-β-D- glucopyranoside from the roots of Limonia crenulata (Roxb.)

Shrivastava, Archana,Parihar, Sangeeta,Jadhav, Raina

, p. 171 - 175 (2013/07/19)

The methanol soluble part of the concent...

New steroidal glycosides from the stem bark of Mimusops elengi

Akhtar,Ali,Alam

experimental part, p. 549 - 553 (2010/12/25)

Two new steroidal glycosides (1 and 2) h...

83-48-7 Process route

22,23-dihydrostigmasteryl methyl ether
139894-63-6,20194-50-7

22,23-dihydrostigmasteryl methyl ether

stigmasterol
83-48-7,481-16-3,32345-19-0,72903-53-8,76250-40-3,80735-61-1,125636-86-4,130061-66-4,139685-48-6,14375-01-0

stigmasterol

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In 1,4-dioxane; water; at 100 ℃; for 2h;
90%
stigmasteryl-3β arachidate

stigmasteryl-3β arachidate

Arachidic acid
506-30-9

Arachidic acid

stigmasterol
83-48-7,481-16-3,32345-19-0,72903-53-8,76250-40-3,80735-61-1,125636-86-4,130061-66-4,139685-48-6,14375-01-0

stigmasterol

Conditions
Conditions Yield
With hydrogenchloride; water; In 1,4-dioxane; for 4h; Reflux;

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