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850528P

Avanti

Mal(11.2)

tridecan-3-yloxy-β-D-maltoside, powder

Synonym(s):

3-tridecyl-Β-D-maltopyranoside

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About This Item

Empirical Formula (Hill Notation):
C25H48O11
CAS Number:
1219008-64-6
Molecular Weight:
524.64
UNSPSC Code:
12161902
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 g (850528P-1g)

manufacturer/tradename

Avanti Research™ - A Croda Brand 850528P

shipped in

dry ice

storage temp.

−20°C

SMILES string

OC[C@H]1O[C@@H](OC(CC)CCCCCCCCCC)[C@H](O)[C@@H](O)[C@@H]1O[C@@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2

General description

This new class of detergents contain a short, branched alkyl chain at the interface between the polar head and the apolar tail. This design mimics the second aliphatic chain of lipid molecules and reduces water penetration, thereby increasing the hydrophobicity within the interior of the micelle. A detergent architecture of this style allows formation of smaller, more compact micelles which provides improved performance in the stabilization and crystallization of integral membrane proteins.

Packaging

20 mL Clear Glass Screw Cap Vial (850528P-1g)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

850528P-1G:
850528P-VAR:
850528P-BULK:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Xiaoxu Jiang et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(12), E698-E704 (2012-02-23)
LacY mutant Cys154 → Gly exhibits a periplasmic-closed crystal structure identical to the WT, but is periplasmic-open in the membrane. The mutant hardly catalyzes transport, but binds galactosides from either side of the membrane with the same affinity and is
Wen-Xu Hong et al.
Langmuir : the ACS journal of surfaces and colloids, 26(11), 8690-8696 (2010-03-18)
A challenging requirement for structural studies of integral membrane proteins (IMPs) is the use of amphiphiles that replicate the hydrophobic environment of membranes. Progress has been impeded by the limited number of useful detergents and the need for a deeper

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