O0630
Octyl α-D-glucopyranoside
≥98% (GC)
Synonim(y):
n-Octyl α-glucoside
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C14H28O6
Numer CAS:
Masa cząsteczkowa:
292.37
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4232620
Pomoc techniczna
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Pozwól nam pomócdescription
non-ionic
assay
≥98% (GC)
mol wt
292.37 g/mol
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-RGDJUOJXSA-N
Application
Octyl α-D-glucopyranoside has been used in a study to assess mesogenic structures with interdigitizing alkyl chains. It has also been used in a study to investigate a recirculation procedure involving water removal by product crystallization.
Biochem/physiol Actions
Dialyzable nonionic detergent, suitable for the solubilization and purification of membrane proteins. Can be used for the crystallization of membrane proteins.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
G A Jeffrey et al.
Carbohydrate research, 169, 1-11 (1987-11-15)
The crystal structure of octyl alpha-D-glucopyranoside monohydrate, C14H28O6.H2O, is monoclinic, C2, with Z = 4, a = 17.896(2), b = 5.154(1), c = 18.303(2) A, beta = 90.30(1) degrees. The hemihydrate, C14H28O6.0.5 H2O, is also monoclinic, C2, with Z =
Efficient Preparation of Octyl α-D-Glucopyranoside Monohydrate: A Recirculation Procedure Involving Water Removal by Product Crystallisation
Straathof, A., et al.
Starch/Staerke, 40, 229-234 (1988)
Jung-Deog Lee et al.
Organic letters, 7(6), 963-966 (2005-03-12)
[structure: see text] Porphyrin-based molecularly imprinted polymers (MIPs) were prepared for carbohydrate recognition. A urea-appended porphyrin functional monomer was utilized to provide complementary functionality and quality binding sites throughout the polymer. Each porphyrin-based polymer demonstrates high affinity and differential selectivity
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| O0630-1G | 04061826061336 |
| O0630-100MG | 04061832392394 |