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Merck
CN

47132

豆甾醇

certified reference material, 10 mg/mL in chloroform

别名:

3β-羟基-24-乙基-5,22-胆甾二烯, 5,22-豆甾二烯-3β-醇, 豆固醇

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关于此项目

经验公式(希尔记法):
C29H48O
化学文摘社编号:
分子量:
412.69
EC Number:
200-663-8
UNSPSC Code:
12164500
PubChem Substance ID:
Beilstein/REAXYS Number:
2568182
MDL number:
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InChI

1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-10,19-21,23-27,30H,7,11-18H2,1-6H3/b9-8+/t20-,21-,23+,24+,25-,26+,27+,28+,29-/m1/s1

InChI key

HCXVJBMSMIARIN-PHZDYDNGSA-N

SMILES string

[H][C@@]12[C@]([C@](CC[C@H](O)C3)(C)C3=CC2)([H])CC[C@@]4(C)[C@@]1([H])CC[C@]4([H])[C@]([H])(C)/C=C/[C@@H](CC)C(C)C

grade

certified reference material, TraceCERT®

product line

TraceCERT®

assay

95% (chromatography)

form

liquid

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

10 mg/mL in chloroform

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

165-167 °C (lit.)

application(s)

food and beverages

format

single component solution

functional group

hydroxyl

storage temp.

2-30°C, room temp

Gene Information

human ... POLA1(5422), TOP2A(7153)
rat ... Polb(29240)

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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.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system, Liver,Kidney

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

易制毒化学品(2类)
危险化学品
此项目有

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P Mangala Gowri et al.
Journal of natural products, 72(4), 791-795 (2009-04-25)
Two new isomeric acylated oleanane-type triterpenoids along with three known compounds were isolated from the MeOH extract of the dried fruits of Barringtonia racemosa. On the basis of spectroscopic methods, with special emphasis on 1D and 2D NMR techniques as
Woo-Suk Jung et al.
Journal of Asian natural products research, 14(4), 301-307 (2012-03-02)
Two new compounds stigmast-5-en-3β-ol-3-O-β-D-(2'-n-triacontanoyl) glucopyranoside (1) and 19,21-dimethyl triacont-17,22,24,26,28-pentaene-1-oic acid (2), along with the three known compounds n-tetracosanyl octadec-9-enoate (3), β-sitosterol, and β-sitosterol-3-O-β-D-glucoside, have been isolated from the methanol extract of Lycium chinense fruits. The structures of these phytoconstituents have
Tae Hoon Lee et al.
International immunopharmacology, 13(3), 264-270 (2012-05-19)
Extracts from the leaves of Stewartia koreana are known to exhibit strong anti-inflammatory activity. Investigation of bioactive compounds from S. koreana has led to the isolation of 3-O-β-d-glucopyanosylspinasterol (spinasterol-Glc), a spinasterol glycoside. In the present study, we examined the effects
Gabriela Trevisan et al.
The Journal of pharmacology and experimental therapeutics, 343(2), 258-269 (2012-07-28)
The transient receptor potential vanilloid 1 (TRPV1) receptor is relevant to the perception of noxious information and has been studied as a therapeutic target for the development of new analgesics. The goal of this study was to perform in vivo
Min-Sang Yoo et al.
Food chemistry, 135(3), 967-975 (2012-09-08)
It has been reported that fucosterol has anti-diabetic, anti-oxidant, and anti-osteoporotic effects. We investigated the anti-inflammatory effects and the underlying molecular mechanism of fucosterol in lipopolysaccharide (LPS)-induced RAW 264.7 macrophages. Fucosterol suppressed the expressions of inducible nitric oxide synthase (iNOS)

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