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47132

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Stigmasterol

certified reference material, 10 mg/mL in chloroform

Synonyme(s) :

3β-hydroxy-24-éthyl-5,22-cholestadiène, 5,22-stigmastadiène-3β-ol

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About This Item

Formule empirique (notation de Hill):
C29H48O
Numéro CAS:
Poids moléculaire :
412.69
Numéro Beilstein :
2568182
Numéro CE :
Numéro MDL:
Code UNSPSC :
12164500
ID de substance PubChem :

Qualité

certified reference material
TraceCERT®

Gamme de produits

TraceCERT®

Pureté

95% (chromatography)

Forme

liquid

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 1 mL

Concentration

10 mg/mL in chloroform

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

165-167 °C (lit.)

Application(s)

food and beverages

Format

single component solution

Groupe fonctionnel

hydroxyl

Température de stockage

2-30°C
room temp

Chaîne SMILES 

[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

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

Clé InChI

HCXVJBMSMIARIN-PHZDYDNGSA-N

Informations sur le gène

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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.

Autres remarques

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.

Informations légales

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

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system, Liver,Kidney

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Les clients ont également consulté

Slide 1 of 4

1 of 4

L Alemany et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(9), 3106-3113 (2012-07-04)
The biological implications of cholesterol oxidation products have been investigated, though research on plant sterol oxidation products is scarce and in some cases contradictory. The cytotoxicity of 7keto(k)-stigmasterol versus 7keto(k)-cholesterol at different concentrations (0-120 μM) and incubation times (4-24h), in
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
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
Verena K Burg et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(41), 16072-16087 (2013-10-11)
Amyloid-β (Aβ), major constituent of senile plaques in Alzheimer's disease (AD), is generated by proteolytic processing of the amyloid precursor protein (APP) by β- and γ-secretase. Several lipids, especially cholesterol, are associated with AD. Phytosterols are naturally occurring cholesterol plant

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