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4-Nitrophenyl ?-D-cellotetraoside is small molecule cellulose mimic that consists of a tetramer of D-glucose units joined by ?-1-4-glycosidic bonds. An aglycosidic bond links a 4-nitrophenyl moiety to the anomeric carbon of the first glucose unit. 4-Nitrophenyl ?-D-cellotetraoside is employed in cellulose degradation studies to determine the specificity of cellulases.{34543,34544,34542} The defined, small, and soluble structure of 4-nitrophenyl ?-D-cellotetraoside makes it well suited for these studies. Its fragmentation pattern after enzymatic digestion can be analyzed by TLC or by release of 4-nitrophenol which exhibits strong absorbance at 395 nm in alkaline solution.{34543,34544,34542}
Territorial Availability: Available through Bertin Technologies only in France
| Size | 1 mg, 500 µg |
|---|---|
| Shipping | dry ice |
| CAS number | 129411-62-7 |
| Molecular formula | C30H45NO23 |
| Smiles | OC[C@H]([C@@H](O[C@@]1([H])[C@H](O)[C@@H](O)[C@H](O[C@]2([H])O[C@H](CO)[C@@H](O[C@@]3([H])[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)[C@H](O)[C@H]2O)[C@@H](CO)O1)[C@H](O)[C@H]4O)O[C@H]4OC5=CC=C([N+]([O-])=O)C=C5 |
| Molecular weight | 787,7 |
| Custom code | 2932.99 |
| Formulation | A solid |
| Purity | ≥99% |
| UNSPSC code | 12352100 |
Cayman Chemical’s mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.
Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.
Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.
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