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15826

Sigma-Aldrich

Tetradecyl-β-D-maltoside

≥99.0% (TLC)

Synonym(s):

n-Tetradecyl β-D-maltopyranoside

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About This Item

Empirical Formula (Hill Notation):
C26H50O11
CAS Number:
Molecular Weight:
538.67
Beilstein:
5458950
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25

description

non-ionic

Assay

≥99.0% (TLC)

form

solid

mol wt

538.67 g/mol

solubility

H2O: 10 mg/mL, clear, colorless

SMILES string

CCCCCCCCCCCCCCO[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/C26H50O11/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-34-25-23(33)21(31)24(18(16-28)36-25)37-26-22(32)20(30)19(29)17(15-27)35-26/h17-33H,2-16H2,1H3/t17-,18-,19-,20+,21-,22-,23-,24-,25-,26-/m1/s1

InChI key

UKPROSIGWJBJGA-IWODYCRQSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Modulation of acetylcholinesterase activity by glycoside-detergents and their solubilization efficiency for neuronal membranes from bovine nucleus caudatus.
P Landauer et al.
Biochemical and biophysical research communications, 106(3), 848-855 (1982-06-15)
Dennis J Pillion et al.
Journal of pharmaceutical sciences, 91(6), 1456-1462 (2002-07-13)
A series of new glycosides with extended alkyl side-chains (C(13-16)) linked to maltose or sucrose were synthesized and tested for their efficacy in enhancing nasal insulin absorption in anesthetized rats. The new reagents were compared to previously tested alkylglycosides with
J Stöckel et al.
European journal of biochemistry, 248(3), 684-691 (1997-10-28)
We investigated the mechanism of refolding and reassembly of recombinant alpha and beta chains of the class II major histocompatibility molecules (MHC-II) HLA-DRB5*0101. Both chains were expressed in the cytosol of Escherichia coli, purified in urea and SDS, and reassembled

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