n-Dodecyl-beta-D-maltopyranoside
n-Dodecyl-beta-D-maltopyranoside
n-Dodecyl-beta-D-maltopyranoside
n-Dodecyl-beta-D-maltopyranoside
Thermo Scientific Chemicals

n-Dodecyl-beta-D-maltopyranoside

A non-ionic detergent useful in membrane solubilization studies | CAS: 69227-93-6 | C24H46O11 | 510.621 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
500 mg
1 g
5 g
Catalog number J66869.ME
also known as J66869-ME
Price (CNY)
-
Quantity:
500 mg
Request bulk or custom format
Chemical Identifiers
CAS69227-93-6
IUPAC Name(2R,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R,6R)-6-(dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC24H46O11
InChI KeyNLEBIOOXCVAHBD-QKMCSOCLSA-N
SMILESCCCCCCCCCCCCO[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
View more
SpecificationsSpecification SheetSpecification Sheet
FormPowder
Assay by NMR≥98.0% (Proton NMR on dry matter)
Water Content (Karl Fischer Titration)≤2.0%
Proton NMRConforms to structure
Optical Rotation+45° to +49° (c=1 in water)
View more
N-dodecyl-β-D-maltoside is used as a non-ionic detergent for stabilization and activation of enzymes and for membrane research. It has also been used for the isolation of the mitochondrial cytochrome c oxidize.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
N-dodecyl-β-D-maltoside is used as a non-ionic detergent for stabilization and activation of enzymes and for membrane research. It has also been used for the isolation of the mitochondrial cytochrome c oxidize.

Solubility
Soluble in water at 10% w/v

Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
RUO – Research Use Only

General References:

  1. Abraham Rubinstein . Colonic drug delivery. Drug Discovery Today: Technologies. 2005, 2, (1), 33-37.
  2. Sam Maher.; David J. Brayden. Overcoming poor permeability: translating permeation enhancers for oral peptide delivery. Drug Discovery Today: Technologies. 2012, 9, (2), e113-e119.