19181
n-Octyl β-D-maltoside
≥99.0% (HPLC)
别名:
n-Octyl β-D-maltopyranoside
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关于此项目
经验公式（希尔记法）:
C20H38O11
化学文摘社编号:
分子量:
454.51
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12161900
MDL number:
产品名称
n-Octyl β-D-maltoside, ≥99.0% (HPLC)
InChI key
MASIZQYHVMQQKI-OIIXUNCGSA-N
SMILES string
CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
InChI
1S/C20H38O11/c1-2-3-4-5-6-7-8-28-19-17(27)15(25)18(12(10-22)30-19)31-20-16(26)14(24)13(23)11(9-21)29-20/h11-27H,2-10H2,1H3/t11-,12-,13-,14+,15-,16-,17-,18-,19-,20-/m1/s1
description
non-ionic
assay
≥99.0% (HPLC)
form
solid
optical activity
[α]/D 58.0±3.0°, c = 1 in H2O
mol wt
average mol wt 38,000
aggregation number
84
impurities
≤0.25% n-octanol
CMC
23.4
solubility
H2O: 100 mg/mL, clear, colorless
application(s)
histology
Quality Level
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Application
Water-soluble non-ionic detergent suitable for solubilization and isolation of membrane proteins.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
涉药品监管产品
此项目有
Andrew R Osborne et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(30), 10937-10942 (2004-07-17)
The ATPase SecA mediates the posttranslational translocation of a wide range of polypeptide substrates through the SecY channel in the cytoplasmic membrane of bacteria. We have determined the crystal structure of a monomeric form of Bacillus subtilis SecA at a
Y Mechref et al.
Chirality, 8(7), 518-524 (1996-01-01)
A chiral alkylglucoside surfactant, namely n-octyl-beta-D-maltopyranoside (OM), was evaluated in the enantiomeric separation of phenoxy acid herbicides. The enantiomeric resolution of the phenoxy acid herbicides could be manipulated readily by adjusting the surfactant concentration, ionic strength, pH, the percent organic
E Meezan et al.
Cellular and molecular biology (Noisy-le-Grand, France), 43(3), 369-381 (1997-05-01)
Glycogenin is a 37 kDa self-glycosylating protein which has been demonstrated to be the initiating enzyme and primer for glycogen biosynthesis in liver, skeletal muscle and other tissues. We have recently shown that glycogenin will use alkylglucosides and alkylmaltosides as
Y Mechref et al.
Electrophoresis, 18(2), 220-226 (1997-02-01)
A novel chiral nonionic surfactant, namely octyl-b-D-maltopyranoside (OM), was evaluated in chiral capillary electrophoresis of fluorescently labeled phenoxy acid herbicides. The labeling of the analytes with 7-aminonaphthalene-1,3-disulfonic acid (ANDSA) permitted a concentration detection limit of 5 x 10-10 M using
M Gabriella Santonicola et al.
Biophysical journal, 94(9), 3647-3658 (2008-02-01)
The binding of alkyl polyglucoside surfactants to the integral membrane protein bacteriorhodopsin (BR) and the formation of protein-surfactant complexes are investigated by sedimentation equilibrium via analytical ultracentrifugation and by small-angle neutron scattering (SANS). Contrast variation techniques in SANS enable measurement
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