69984-73-2
Chemical Structure
Nonyl β-D-glucopyranoside
Synonym(s): n-Nonyl-β-D-glucopyranoside
- CAS No.: 69984-73-2
- Formula:C15H30O6
- Molecular Weight:306.40
IUPAC Name: (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(nonyloxy)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: QFAPUKLCALRPLH-UXXRCYHCSA-N
SMILES: CCCCCCCCCO[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO
Biological Activity: Nonyl β-D-glucopyranoside (n-Nonyl-β-D-glucopyranoside) is a surfactant that can be used in studies on interactions with lipid monolayers. Nonyl β-D-glucopyranoside can also be used for the enantiomer separation of phenoxy acid herbicides and amino acid derivatives[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Nonyl β-D-glucopyranoside | 99.92% | Nonyl β-D-glucopyranoside (n-Nonyl-β-D-glucopyranoside) is a surfactant that can be used in studies on interactions with lipid monolayers. Nonyl β-D-glucopyranoside can also be used for the enantiomer separation of phenoxy acid herbicides and amino acid derivatives. | ||||||||||||||||||||
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- [1]. Annette Meister, et al. The interaction of n-nonyl-β-d-glucopyranoside and sodium dodecyl sulfate with DMPC and DMPG monolayers studied by infrared reflection absorption spectroscopy. Phys. Chem. Chem. Phys., 2004,6, 5543-5550
- [2]. Otsuka K, et al. Enantiomer separation of drugs by micellar electrokinetic chromatography using chiral surfactants. J Chromatogr A. 2000 Apr 14;875(1-2):163-78. [Content Brief]
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