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n-Dodecyl-β-D-maltoside

Catalog No.
C4421
A non-ionic detergent commonly used to solubilize membrane-associated proteins
Grouped product items
SizePriceStock Qty
500mg
$58.00
In stock
1g
$95.00
In stock
5g
$211.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

n-Dodecyl-β-D-maltoside (CAS No.: 69227-93-6) is a widely used non-ionic detergent belonging to the class of alkyl maltosides, primarily employed in biochemical and biophysical research for the solubilization, stabilization, and functional reconstitution of membrane-associated proteins. Derived from maltose and a hydrophobic alkyl chain, this compound effectively preserves the native conformation and biological activity of integral membrane proteins, making it particularly valuable in studies of protein structure, enzymatic function, and protein–lipid interactions. Its mechanism of action involves the gentle disruption of lipid bilayers and formation of micelles that encapsulate hydrophobic protein domains, thereby preventing aggregation and denaturation; it also exhibits notable adsorption properties on metal oxide surfaces, which can influence protein-surface interactions in experimental systems. n-Dodecyl-β-D-maltoside has been shown to promote the reactivation and stabilization of diverse proteins, including photoactive reaction center complexes, where it inhibits degradation and maintains functional integrity in solution. It is extensively utilized in the purification and stabilization of multi-subunit complexes such as RNA polymerase, as well as in assays probing membrane protein folding and protein–lipid binding dynamics. With a relatively low critical micelle concentration in aqueous environments, its performance is modulated by solution conditions such as ionic strength and denaturant presence, which can impact micelle formation and protein compatibility. In vitro applications typically involve low micromolar to millimolar concentrations depending on the target protein and assay system, and its use in cell-free systems, reconstituted membranes, and structural biology workflows supports drug discovery efforts targeting membrane proteins, including receptors, channels, and transporters.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt510.62
Cas No.69227-93-6
FormulaC24H46O11
SynonymsDDM; Dodecyl Maltoside
Solubility≥36.75 mg/mL in DMSO; ≥51.1 mg/mL in H2O with ultrasonic; ≥9.6 mg/mL in EtOH
Chemical Name(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-6-(dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
Canonical SMILESOC[C@@H]1[C@H]([C@@H]([C@H]([C@]([H])(O1)O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2CO)OCCCCCCCCCCCC)O)O)O)O)O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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