75081
Octyl D-glucopyranoside
mixture of anomers, α-anomer/β-anomer ~7:3, ~80% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C14H28O6
CAS Number:
Molecular Weight:
292.37
Beilstein/REAXYS Number:
4864266
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
description
non-ionic
assay
~80% (TLC)
form
paste
mol wt
292.37 g/mol
loss
≤10% loss on drying
color
beige
SMILES string
CCCCCCCCOC1O[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-RQICVUQASA-N
Other Notes
For the crystallisation of membrane proteins[1]
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Respiratory complex I is a redox-driven proton pump, accounting for a large part of the electrochemical gradient that powers mitochondrial adenosine triphosphate synthesis. Complex I dysfunction is associated with severe human diseases. Assembly of the one-megadalton complex I in the
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The dimorphic transition from the yeast to the filamentous form of growth allows cells to explore their environment for more suitable niches and is often crucial for the virulence of pathogenic fungi. In contrast to their Mep1/3 paralogues, fungal Mep2-type
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The immunopathological mechanisms as well as the role played by influenza A virus infection of human leukocytes and induction of apoptosis have not been fully elucidated. We confirm here that the percentage of cells that are infected is less than
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