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O9882

辛基-β-D-吡喃葡萄糖苷

Name: 辛基-β-<SC>D</SC>-吡喃葡萄糖苷
Brand: SIAL

BioXtra, ≥98% (GC)

别名:

OGP, 正辛基葡萄糖苷

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关于此项目

经验公式（希尔记法）:

C₁₄H₂₈O₆

化学文摘社编号:

29836-26-8

分子量:

292.37

UNSPSC Code:

12161900

NACRES:

NA.21

PubChem Substance ID:

24898076

EC Number:

249-887-8

Beilstein/REAXYS Number:

84118

MDL number:

MFCD00063288

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属性

description

non-ionic

Quality Level

200

product line

BioXtra

assay

≥98% (GC)

form

powder

mol wt

micellar avg mol wt 25,000

aggregation number

impurities

≤0.005% Phosphorus (P), ≤0.1% Insoluble matter

ign. residue

≤0.2%

CMC

20-25 mM (20-25°C)

transition temp

cloud point >100 °C

anion traces

chloride (Cl^-): ≤0.05%, sulfate (SO₄^2-): ≤0.05%

cation traces

Al: ≤0.0005%, Ca: ≤0.003%, Cu: ≤0.0005%, Fe: ≤0.0005%, K: ≤0.005%, Mg: ≤0.0005%, NH₄⁺: ≤0.1%, Na: ≤0.1%, Pb: ≤0.001%, Zn: ≤0.0005%

storage temp.

−20°C

SMILES string

CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1

InChI key

HEGSGKPQLMEBJL-RKQHYHRCSA-N

说明

Application

辛基β-D-吡喃葡萄糖苷已被用作含有NaCl、HEPES和显色底物的水性缓冲液的组分，用于胰蛋白酶测定

用于溶解和分离膜蛋白的非离子型可透析洗涤剂。已证明可提高 2D 凝胶中蛋白质的分离度。

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存储类别

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives.

Bioorganic & Medicinal Chemistry Letters, 18(6), 2114-2121 (2008)

Hydrogen bonds in galactopyranoside and glucopyranoside: a density functional theory study.

Zahrabatoul Mosapour Kotena et al.

Journal of molecular modeling, 19(2), 589-599 (2012-09-14)

Density functional theory calculations on two glycosides, namely, n-octyl-β-D-glucopyranoside (C(8)O-β-Glc) and n-octyl-β-D-galactopyranoside (C(8)O-β-Gal) were performed for geometry optimization at the B3LYP/6-31G level. Both molecules are stereoisomers (epimers) differing only in the orientation of the hydroxyl group at the C4 position.

Structurally diverse amphiphiles exhibit biphasic modulation of GABAA receptors: similarities and differences with neurosteroid actions.

M Chisari et al.

British journal of pharmacology, 160(1), 130-141 (2010-04-24)

Some neurosteroids, notably 3alpha-hydroxysteroids, positively modulate GABA(A) receptors, but sulphated steroids negatively modulate these receptors. Recently, other lipophilic amphiphiles have been suggested to positively modulate GABA receptors. We examined whether there was similarity among the actions of these agents and

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全球贸易项目编号

货号	GTIN
O9882-100MG	04061833435588
O9882-500MG	04061833435601
O9882-5G	04061833429259
O9882-250MG	04061833435595
O9882-1G	04061834248972