29836-26-8
29836-26-8
Chemical Structure
n-Octyl β-D-glucopyranoside
- CAS No.: 29836-26-8
- Formula:C14H28O6
- Molecular Weight:292.37
IUPAC Name: (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(octyloxy)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: HEGSGKPQLMEBJL-RKQHYHRCSA-N
SMILES: O[C@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)[C@@H]1OCCCCCCCC
Biological Activity: n-Octyl-β-d-glucopyranoside is a non-ionic detergent, it can be widely used in the research of biotechnical, biochemical applications, solubilization and crystallization of membrane proteins. n-Octyl-β-d-glucopyranoside can completely inhibit cavitation-induced cell lysis in vitro[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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n-Octyl β-D-glucopyranoside | 99.93% | n-Octyl-β-d-glucopyranoside is a non-ionic detergent, it can be widely used in the research of biotechnical, biochemical applications, solubilization and crystallization of membrane proteins. n-Octyl-β-d-glucopyranoside can completely inhibit cavitation-induced cell lysis in vitro. | ||||||||||||||||||||
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n-Octyl β-D-glucopyranoside-d24 | 98.7% | n-Octyl β-D-glucopyranoside-d24 is the deuterium labeled n-Octyl β-D-glucopyranoside (HY-116285). | ||||||||||||||||||||
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1-O-n-Octyl-β-D-glucopyranoside-d17 | 98.1% | 1-O-n-Octyl-β-D-glucopyranoside-d17 is the deuterium labeled n-Octyl β-D-glucopyranoside. n-Octyl-β-d-glucopyranoside is a non-ionic detergent, it can be widely used in the research of biotechnical, biochemical applications, solubilization and crystallization of membrane proteins. | ||||||||||||||||||||
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References
- [1]. Konidala P, et al. Molecular dynamics characterization of n-octyl-beta-D-glucopyranoside micelle structure in aqueous solution. J Mol Graph Model. 2006 Sep;25(1):77-86. [Content Brief]
- [2]. Gould RJ, et al. Effects of octyl beta-glucoside on insulin binding to solubilized membrane receptors. Biochemistry. 1981 Nov 24;20(24):6776-81. [Content Brief]
- [3]. Douglas L Miller, et al. The influence of octyl β-D-glucopyranoside on cell lysis induced by ultrasonic cavitation. J Acoust Soc Am. 2011 Nov;130(5):3482-8. [Content Brief]
