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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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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

Related Categories

General description

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.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

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

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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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
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
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
Yu-Feng Xie et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(3), 386-388 (2011-08-10)
To study the chemical constituents from Melicope ptelefolia. Several chromatographic methods were applied to isolate and purify compounds. Their structures were identified on the basis of physicochemical properties and spectroscopic data. Seven compounds were isolated and elucidated as n-octadecanyl palmitate
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