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89851

Supelco

β-Sitosterol β-D-glucoside

analytical standard

Sinonimo/i:

β-Daucosterol, Coriandrinol, Daucosterin, Eleutheroside A

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About This Item

Formula empirica (notazione di Hill):
C35H60O6
Numero CAS:
474-58-8
Peso molecolare:
576.85
Codice UNSPSC:
85151701
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥75.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Stringa SMILE

CC[C@H](CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)O[C@@H]5OC(CO)[C@@H](O)[C@H](O)C5O)C(C)C

InChI

1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1
NPJICTMALKLTFW-OFUAXYCQSA-N

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Categorie correlate

Descrizione generale

β-Sitosterol β-D-glucoside is a steroid glycoside having, β-sitosterol as the aglycone.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Altre note

This compound is commonly found in plants of the genus: triticum withania serenoa

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

681.8 °F

Punto d’infiammabilità (°C)

361 °C

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG4972
BCCC6891
BCBZ6335
BCBT5584
BCBR7181V

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β-Sitosterol primary reference standard

02090580

β-Sitosterol

β-Sitosterol ≥70%

Sigma-Aldrich

85451

β-Sitosterol

β-Sitosterol from soybean, ≥96%

Sigma-Aldrich

S9889

β-Sitosterol

Pectolinarigenin phyproof® Reference Substance

PHL82621

Pectolinarigenin

β-Sitosterol certified reference material, 100 μg/mL in chloroform

Supelco

47133

β-Sitosterol

Friedelin technical grade

Sigma-Aldrich

855022

Friedelin

Fucosterol ≥93%

Sigma-Aldrich

F5379

Fucosterol

Xin-Ping Cheng et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 33(11), 1727-1730 (2011-03-26)
To study the chemical constituents of the root tube from Pteroxygonum giraldii. Column chromatography and spectral analysis were used to isolate and identify the constituents. Ten compounds were isolated and identified as beta-sitosterol (I), beta-sitosterol glucoside (II), 4', 5,5', 7-tetrahydroxy-3'-methoxy-3'-O-alpha-L-arabinopyranosyl
Tang W and Eisenbrand G et al.
Chinese Drugs of Plant Origin: Chemistry, Pharmacology, and Use in Traditional and Modern Medicine (2013)
Yunfei Chen et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 37(7), 946-950 (2012-07-17)
To study sesquiterpenoids of Coniogramme maxima. Chemical constituents were separated by chromatography and their structures were identified according to physicochemical property and spectrum data. Fifteen compounds were separated by chromatography technique. Their structures were determined by spectral data, including 10
Wirongrong Kaweetripob et al.
Phytochemistry, 76, 78-82 (2012-02-10)
5-Formylfurfuryl esters, duabanganals A-D, together with sixteen known compounds, a known 5-formylfurfuryl ester, latifolinal, eight pentacyclic triterpenes, a benzofuran derivative, an ellagic acid derivative, vanillin, β-sitosterol, β-sitosterol glucoside, 3-hydroxy-4-methoxycinnamaldehyde, and 5-formylfurfurol, were isolated from the stem bark of Duabanga grandiflora.
Huan-Kai Yao et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(5), 716-718 (2011-10-01)
To investigate the chemical constituents of Kalopanax septemlobus. Chromatographic techniques including silica gel, gel, semi-preparative HPLC and PTLC as well as recrystallization were employed in the isolation and purification, and the structures were elucidated by spectral analysis and physical and
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