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Fórmula empírica (notación de Hill):
C14H28O6
Número CAS:
Peso molecular:
292.37
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4232620
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Permítanos ayudarledescription
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. [1] 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.
Clase de almacenamiento
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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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
Brown, G.M., et al.
Canadian Journal of Chemistry, 48, 2525-2525 (1970)
J D Doran et al.
Journal of pharmaceutical sciences, 101(1), 92-101 (2011-09-17)
Membrane proteins are attractive therapeutic targets, however the presence of detergents complicates biophysical binding measurements. Difficulties in determining quantitative dissociation constants for problematic membrane proteins were addressed by combining analytical ultracentrifugation and classical light scattering techniques. Validation of the algorithm
Número de artículo de comercio global
| SKU | GTIN |
|---|---|
| O0630-1G | 04061826061336 |
| O0630-100MG | 04061832392394 |
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