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D7658

Decyl β-D-maltopyranoside

≥98% (GC)

Synonym(s):

Decyl-β-D-maltoside

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About This Item

Empirical Formula (Hill Notation):
C22H42O11
CAS Number:
82494-09-5
Molecular Weight:
482.56
Beilstein:
4923334
MDL number:
MFCD00061624
UNSPSC Code:
12161900
PubChem Substance ID:
24894148
NACRES:
NA.25

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description

non-ionic

Quality Level

100

Assay

≥98% (GC)

form

powder

mol wt

482.56 g/mol

CMC

1.6 mM (20-25°C)
1.6-1.8

storage temp.

−20°C

SMILES string

CCCCCCCCCCO[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/C22H42O11/c1-2-3-4-5-6-7-8-9-10-30-21-19(29)17(27)20(14(12-24)32-21)33-22-18(28)16(26)15(25)13(11-23)31-22/h13-29H,2-12H2,1H3/t13-,14-,15-,16+,17-,18-,19-,20-,21-,22-/m1/s1

InChI key

WOQQAWHSKSSAGF-WXFJLFHKSA-N

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This Item
324355252718D5172
Decyl β-D-maltopyranoside ≥98% (GC)

Sigma-Aldrich

D7658

Decyl β-D-maltopyranoside

n-Dodecyl β-D-maltoside ULTROL® Grade, ≥98% (HPLC), non-ionic detergent for the stabilization and activation of enzymes

Millipore

324355

n-Dodecyl β-D-maltoside

Decyl-β-D-maltopyranoside ULTROL® Grade, ≥99% (HPLC), non-ionic detergent for solubilization of membrane-bound proteins

Millipore

252718

Decyl-β-D-maltopyranoside

n-Dodecyl β-D-maltoside BioXtra, ≥98% (GC)

Sigma-Aldrich

D5172

n-Dodecyl β-D-maltoside

assay

≥98% (GC)

assay

≥98% (HPLC)

assay

≥99% (HPLC)

assay

≥98% (GC)

form

powder

form

solid

form

lyophilized

form

powder

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

description

non-ionic

description

-

description

-

description

non-ionic

mol wt

482.56 g/mol

mol wt

micellar wt 50000

mol wt

-

mol wt

micellar avg mol wt 50,000

CMC

1.6 mM (20-25°C), 1.6-1.8

CMC

100-600 μM

CMC

1.6 mM

CMC

0.15 mM (20-25°C)

General description

Decyl β-D-maltopyranoside is a nonionic detergent. [1]

Application

Decyl β-D-maltopyranoside has been used in a study to assess α-helical membrane protein crystallization. [2] It has also been used in a study to investigate enantiomer separation of drugs by micellar electrokinetic chromatography. [3]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2161
BCCC3161
BCCB8380
BCCB0101
BCBZ5154

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Simon Newstead et al.
Protein science : a publication of the Protein Society, 17(3), 466-472 (2008-01-26)
X-ray crystallography is currently the most successful method for determining the three-dimensional structure of membrane proteins. Nevertheless, growing the crystals required for this technique presents one of the major bottlenecks in this area of structural biology. This is especially true
B Andersen et al.
FEBS letters, 311(2), 169-173 (1992-10-19)
A photosystem I complex containing the polypeptides PSI-A to PSI-L, light-harvesting complex I and ferredoxin:NADP+ oxidoreductase has been isolated from barley using the non-ionic detergent n-decyl-beta-D-maltopyranoside. The ratio between bound ferredoxin:NADP+ oxidoreductase and P700 is 0.4 +/- 0.2. The complex
K Otsuka et al.
Journal of chromatography. A, 875(1-2), 163-178 (2000-06-06)
A review surveying enantiomer separations by micellar electrokinetic chromatography (MEKC) using chiral surfactants is described. MEKC is one of the most popular techniques in capillary electrophoresis, where neutral compounds can be analyzed as well as charged ones, and the use

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Solubilization of Membrane Proteins

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