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Merck
CN

89851

β-Sitosterol β-D-glucoside

analytical standard

Synonym(s):

β-Daucosterol, Coriandrinol, Daucosterin, Eleutheroside A

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About This Item

Empirical Formula (Hill Notation):
C35H60O6
CAS Number:
474-58-8
Molecular Weight:
576.85
MDL number:
MFCD01683621
UNSPSC Code:
85151701
NACRES:
NA.24

Key Documents

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Product Name

β-Sitosterol β-D-glucoside, analytical standard

SMILES string

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

InChI key

NPJICTMALKLTFW-OFUAXYCQSA-N

grade

analytical standard

assay

≥75.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

Quality Level

100

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Application

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

General description

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

Other Notes

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

681.8 °F

flash_point_c

361 °C

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8680
BCCJ6903
BCCH5037
BCCG4972
BCCC6891

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Qian-Liang Chen et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(8), 1214-1216 (2012-01-12)
To systematically study the chemical constituents in the roots of Gentiana dahurica. Various column chromatographic techniques were used for isolation and purification. The structures were elucidated on the basis of spectral data (UV, IR, MS, NMR) and identified by comparing
Jia-ming Sun et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(7), 1057-1059 (2011-11-10)
To study the chemical constituents of the aerial part of Ligusticum jeholense. The constituents were isolated by sillica gel column chromatography, Sephadex LH-20 column chromatography and their structures were elucidated by spectral analysis. Seven compounds were separated from the EtOH
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
Tang W and Eisenbrand G et al.
Chinese Drugs of Plant Origin: Chemistry, Pharmacology, and Use in Traditional and Modern Medicine (2013)
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.
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