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47132

Supelco

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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About This Item

经验公式（希尔记法）:
C29H48O
CAS号:
83-48-7
分子量:
412.69
Beilstein:
2568182
EC號碼:
200-663-8
MDL號碼:
MFCD00003630
分類程式碼代碼:
12164500
PubChem物質ID:
24870720

等級

certified reference material
TraceCERT®

產品線

TraceCERT®

化驗

95% (chromatography)

形狀

liquid

CofA

current certificate can be downloaded

包裝

ampule of 1 mL

濃度

10 mg/mL in chloroform

技術

HPLC: suitable
gas chromatography (GC): suitable

mp

165-167 °C (lit.)

應用

food and beverages

格式

single component solution

官能基

hydroxyl

儲存溫度

2-30°C
room temp

SMILES 字串

[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

InChI 密鑰

HCXVJBMSMIARIN-PHZDYDNGSA-N

基因資訊

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

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應用

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

其他說明

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.

法律資訊

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

象形圖

Skull and crossbonesHealth hazard
GHS06,GHS08

訊號詞

Danger

危險分類

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

標靶器官

Central nervous system, Liver,Kidney

儲存類別代碼

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

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
LRAD4231
LRAC3872
XA26157V
XA26101V
XA17176V

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β-谷甾醇 synthetic, ≥95%

Sigma-Aldrich

S1270

β-谷甾醇

β-谷甾醇 primary reference standard

02090580

β-谷甾醇

谷甾烷醇 β-sitostanol, powder

Avanti

700121P

谷甾烷醇

Sigma-Aldrich

Sigma-Aldrich

S462330

STIGMASTANOL

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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