1900-52-3

Usage

Uses

Used in Pharmaceutical Industry:
(3beta)-stigmast-5-en-3-yl benzoate is used as a precursor for the synthesis of other biologically active compounds due to its potential therapeutic properties, such as anti-inflammatory and antioxidant effects.
Used in Food Industry:
(3beta)-stigmast-5-en-3-yl benzoate is used as a food additive, leveraging its properties to enhance the quality and shelf life of food products.
Used in Cosmetic Industry:
(3beta)-stigmast-5-en-3-yl benzoate is used in the formulation of cosmetic products, taking advantage of its potential therapeutic properties to provide benefits to the skin and hair.
Used in Drug Delivery Systems:
(3beta)-stigmast-5-en-3-yl benzoate has been investigated for its potential role in the development of novel drug delivery systems, aiming to improve the efficacy and targeted delivery of therapeutic agents.

InChI:InChI=1/C36H54O2/c1-7-26(24(2)3)14-13-25(4)31-17-18-32-30-16-15-28-23-29(38-34(37)27-11-9-8-10-12-27)19-21-35(28,5)33(30)20-22-36(31,32)6/h8-12,15,24-26,29-33H,7,13-14,16-23H2,1-6H3/t25-,26-,29+,30+,31-,32+,33+,35+,36-/m1/s1

Upstream product

• 83-46-5 β-sitosterol 
• 98-88-4 benzoyl chloride 
• 93-97-0 benzoic acid anhydride 
• 101047-07-8 Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-17-((1R,4R)-4-isopropyl-1-methyl-5-phenoxythiocarbonyloxy-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-05-6 Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-17-((1R,4R)-5-hydroxy-4-isopropyl-1-methyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-03-4 24R-isopropenylcholesterol benzoate 
• 101047-04-5 Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-17-((1R,4R)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-05-6 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4S)-5-hydroxy-4-isopropyl-1-methyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-03-4 24 (R/α)-isopropenylcholesterol benzoate 
• 101047-04-5 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4S)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-05-6 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-5-hydroxy-4-isopropyl-1-methyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-03-4 24 (S/β)-isopropenylcholesterol benzoate 
• 101047-04-5 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-07-8 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-4-isopropyl-1-methyl-5-phenoxythiocarbonyloxy-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 

Downstream Products

• 59157-67-4 Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-17-((1R,4R)-4-ethyl-1,5-dimethyl-hexyl)-10,13-dimethyl-7-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 171369-27-0 3β-benzoyloxystigmast-4-en-6β-ol 
• 73336-53-5 (24R)-5-bromo-3β-hydroxy-5α-stigmast-3β,6β-diol-3-benzoate 
• 113626-76-9 stigmast-4-ene-3β,6β-diol 
• 287110-53-6 (24R)-5-bromo-3β-hydroxy-5α-stigmastan-6-one benzoate 
• 287110-54-7 (24R)-3β-hydroxy-7α-bromo-5α-stigniastan-6-one benzoate 
• 287110-55-8 (24R)-3β-hydroxy-5α-stigmast-7-en-6-one benzoate 

Relevant academic research and scientific papers

STEROL PURIFICATION

The invention relates to sterol esters and methods for producing purified sterols that can be utilized in methods for producing a lipid nanoparticle.

Extraction, Isolation and Characterization of Valuable Worked on Acacia Tortilis

Acacia tortilis is one of the important species of genus Acacia belonging to family Leguminaceae. Though there is no more study performed on this plant but it plays important role in the countries where it found. These countries include North Africa, Arabian Peninsula and Asian countries. The various part of Acacia tortilis plant say leaves, pods, gum exudates and bark were used as antidiabetic, antidiarrhoeal, antiasthmatic and also had several other medicinal benefits. The present discussion deals with the isolation and characterization of the following compounds from the leaves of Acacia tortilis. Lupan-3-ol, 12,20-diene, Lupan-12, 20-dien 3-one, Friedelin, ?-amyrin, ?- sitosterol, Apigenin, Luteolin, Quercetin, 5,7-dihydroxy-4-p-methyl benzylisoflavone, Vitexin, 2',6'-dihydroxy chalcone-4'-O-glucoside.

Structures of five hydroxylated sterols from the seeds of Trichosanthes kirilowii maxim

Five hydroxylated sterols, stigmastane-3β,6α-diol, poriferastane- 3β,6α-diol, stigmast-5-ene-3β,4β-diol, poriferast-5-ene-3β,4β-diol, and poriferasta-5,25-diene-3β,4β-diol, the latter four of which are new naturally occurring compounds, were isolated from the unsaponifiable lipid of the seed extract of Trichosanthes kirilowii MAXIM. The structures were determined by spectral and chemical methods.

Studies on the Constituents of Orchidaceous Plants. VII. The C-24 Stereochemistry of Cyclohomonervilol and 24-Isopropenylcholesterol, Non-conventional Side Chain Triterpene and Sterol, from Nervilia purpurea SCHLECHTER

The C-24 stereochemistry of cyclohomonervilol,a non-conventional side chain triterpene isoleted from Nervilia purpurea was determined to be 24S by chemical transformation to 24S-dihydrocyclofuntumienol.Separation of a 24-epimeric mixture of chemically syn

EFFECTIVE SEPARATION AND C-24 STEREOCHEMICAL ASSIGNMENT OF EPIMERIC 24-ISOPROPENYLCHOLESTEROLS

Separation of epimeric 24-isopropenylcholesterols (1a) was effectively achieved by reversed-phase HPLC.The C-24 stereochemistry of these epimers was determined on the basis of chemical and spectroscopic evidence.