Chemodex

Octyl-beta-D-glucopyranoside

Product Code:
 
CDX-O0004
Product Group:
 
Detergents
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
AMBIENT
Storage:
 
Short Term: +4°C, Long Term: -20°C
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Chemical Structure
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Chemical Structure

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CDX-O0004-G0011 g£53.00
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Further Information

Alternate Names/Synonyms:
n-Octyl glucoside; OGP; BTB 11967
Appearance:
White to off-white powder.
CAS:
29836-26-8
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Protect from light and moisture.
InChi:
InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1
InChiKey:
HEGSGKPQLMEBJL-RKQHYHRCSA-N
Long Description:
Chemical. CAS: 29836-26-8. Formula: C14H28O6. MW: 292.34. n-Octylglucoside is a mild, non-denaturing detergent that is used for the solubilization and reconstitution of membrane-bound proteins. The high critical micelle concentration (0.7%) of n-octylglucoside facilitates ready removal from final protein extracts by dialysis or gel filtration. n-Octylglucoside can be used in 2D electrophoresis and to improve selectivity of immunoprecipitation of phosphotyrosine modified proteins.
MDL:
MFCD00063288
Molecular Formula:
C14H28O6
Molecular Weight:
292.34
Package Type:
Vial
Product Description:
n-Octylglucoside is a mild, non-denaturing detergent that is used for the solubilization and reconstitution of membrane-bound proteins. The high critical micelle concentration (0.7%) of n-octylglucoside facilitates ready removal from final protein extracts by dialysis or gel filtration. n-Octylglucoside can be used in 2D electrophoresis and to improve selectivity of immunoprecipitation of phosphotyrosine modified proteins.
Purity:
>98% (HPLC)
SMILES:
O[C@@H]1[C@@H](CO)O[C@@H](OCCCCCCCC)[C@H](O)[C@H]1O
Solubility Chemicals:
Soluble in DMSO (10mg/ml), DMF (10mg/ml) or ethanol (20mg/ml).
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) W.A. Petri & R.R. Wagner; J. Biol. chem. 254, 4313 (1979) | (2) J.S. Lazo & D.E. Quinn; Anal. Biochem. 102, 68 (1980) | (3) S.J. LeGrue, et al.; J. Natl. Cancer Inst. 69, 131 (1982) | (4) B. Lorber, et al.; Biochim. Biophys. Acta 1023, 254 (1990) | (5) W.R. Wenk, et al.; Biophys. J. 72, 1719 (1997) | (6) P. Konidala, et al.; J. Mol. Graph. Model 25, 77 (2006) | (7) G. Zhang & T.A. Neubert; Proteomics 6, 571 (2006)