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Autres documents

89851

Supelco

β-Sitosterol β-D-glucoside

analytical standard

Synonyme(s) :

β-Daucosterol, Coriandrinol, Daucosterin, Eleutheroside A

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About This Item

Formule empirique (notation de Hill):
C35H60O6
Numéro CAS:
474-58-8
Poids moléculaire :
576.85
Code UNSPSC :
85151701

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥75.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

food and beverages

Format

neat

Chaîne SMILES 

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

Clé InChI

NPJICTMALKLTFW-OFUAXYCQSA-N

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Catégories apparentées

Description générale

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

Application

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

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

681.8 °F

Point d'éclair (°C)

361 °C

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG4972
BCCC6891
BCBZ6335
BCBT5584
BCBR7181V

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Sigma-Aldrich

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Sigma-Aldrich

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Pectolinarigenin phyproof® Reference Substance

PHL82621

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Supelco

47133

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Friedelin technical grade

Sigma-Aldrich

855022

Friedelin

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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