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D8035

n-Dodecyl β-D-Glucopyranosid

≥98% (GC)

Synonym(e):

Dodecyl-glucosid

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Über diesen Artikel

Empirische Formel (Hill-System):
C18H36O6
CAS-Nummer:
59122-55-3
Molekulargewicht:
348.47
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24894182
EC Number:
261-614-4
Beilstein/REAXYS Number:
86236
MDL number:
MFCD00063298

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InChI

1S/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18-/m1/s1

InChI key

PYIDGJJWBIBVIA-UYTYNIKBSA-N

SMILES string

CCCCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

description

non-ionic

assay

≥98% (GC)

form

powder

mol wt

348.47 g/mol

technique(s)

protein quantification: suitable

CMC

0.13

solubility

methanol: soluble 50 mg/mL, clear to very slightly hazy, colorless

storage temp.

−20°C

Quality Level

200

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Dieser Artikel
D5394M0779O9882
n-Dodecyl β-D-glucopyranoside ≥98% (GC)

Sigma-Aldrich

D8035

n-Dodecyl β-D-glucopyranoside

Decyl β-D-glucopyranoside ≥98% (GC)

Sigma-Aldrich

D5394

Decyl β-D-glucopyranoside

Methyl β-D-glucopyranoside ≥99% (HPLC and GC)

Sigma-Aldrich

M0779

Methyl β-D-glucopyranoside

Octyl β-D-glucopyranoside BioXtra, ≥98% (GC)

Sigma-Aldrich

O9882

Octyl β-D-glucopyranoside

technique(s)

protein quantification: suitable

technique(s)

protein purification: suitable, protein quantification: suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

assay

≥98% (GC)

assay

≥98% (GC)

assay

≥99% (HPLC and GC)

assay

≥98% (GC)

form

powder

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

storage temp.

−20°C

CMC

0.13

CMC

2.2

CMC

-

CMC

20-25 mM (20-25°C)

mol wt

348.47 g/mol

mol wt

320.42 g/mol

mol wt

-

mol wt

micellar avg mol wt 25,000

Application

Dodecyl β--D-glucopyranoside, a long chain alkyl glycopyranoside and a classical nonionic amphiphile surfactant, is used in detergent and colloid research and micelle development.[1] It may be used as a reference compound in long-chain alkyl glucoside separation and analysis procedures.[2]

Biochem/physiol Actions

Non-ionic saccharide detergent used for the solubilization of membrane-bound proteins, such as G-Protein-Coupled Receptors, in native state

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
0000487065
0000487065
0000416349
0000416349
0000324773

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Y Daicho et al.
Biochimica et biophysica acta, 1107(1), 61-69 (1992-06-11)
A study of the effects of alkyl glycosides incorporated into synthetic liposomes with respect to their stability, their in vivo distribution in Ehrlich solid tumor-bearing mice and their in vitro interaction with liver cells was undertaken. The synthetic liposomes were
S H El-Sharkawy
Australasian biotechnology, 6(1), 8-12 (1996-01-01)
A number of microorganisms has been screened for growth on sunflower oil as a sole carbon source for production of useful chemicals. Rhizopus stolonifer NRRL 1478 was found to transform the lipid contents of sunflower oil into dodecyl b-D-glucopyranoside and
Caroline A Ericsson et al.
Carbohydrate research, 340(8), 1529-1537 (2005-05-11)
The solid-state phase behaviour of lyophilised n-dodecyl-beta-D-glucoside (beta-C(12)G(1)), n-dodecyl-beta-D-maltoside (beta-C(12)G(2)) and n-dodecyl-beta-D-maltotrioside (beta-C(12)G(3)) has been investigated by differential scanning calorimetry (DSC) and X-ray techniques. For beta-C(12)G(1), lyophilisation results in a formation of a crystalline anhydrate. The lamellar spacing (37 Angstroms)
R R Loo et al.
Protein science : a publication of the Protein Society, 3(11), 1975-1983 (1994-11-01)
Electrospray ionization mass spectrometry (ESI-MS) has proven to be a useful tool for examining noncovalent complexes between proteins and a variety of ligands. It has also been used to distinguish between denatured and refolded forms of proteins. Surfactants are frequently
J Lu et al.
Biochemical and biophysical research communications, 196(1), 12-17 (1993-10-15)
Kinetic analyses indicate that the inhibitory effects of the nonionic detergents Triton X-100 and Nonidet P-40 on chloramphenicol acetyltransferase are exerted by a competitive and a non-competitive mechanism with respect to the substrates chloramphenicol and acetyl-CoA, respectively. Comparison with nonionic
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