ChemicalBook > Product Catalog > Biochemical Engineering > Saccharides > Monosaccharide > P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE Basic information
- Product Name:
- P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE
- Synonyms:
-
- 3-Nitrophenyl ?L-rhamnopyranoside
- p-Nitrophenyl alpha-L-rhamnoside
- 3-Nitrophenyl a-L-rhaMnopyranoside
- p-nitrophenyl α-L-Rhap
- 3-Nitrophenyl alpha-L-rhamnopyranoside
- P-NITROPHENYL-ALPHA-RHAMNOSIDE
- P-NITROPHENYL ALPHA-L-RHAMNOPYRANOSIDE
- P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE
- CAS:
- 18918-31-5
- MF:
- C12H15NO7
- MW:
- 285.25
- EINECS:
- 1592732-453-0
- Mol File:
- 18918-31-5.mol
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P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE Chemical Properties
- Melting point:
- 179°C
- Boiling point:
- 515.4±50.0 °C(Predicted)
- Density
- 1.503±0.06 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 0.25 mg/ml; PBS (pH 7.2): 2 mg/ml
- form
- powder
- pka
- 12.68±0.70(Predicted)
- LogP
- 1.170 (est)
MSDS
- Language:English Provider:SigmaAldrich
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P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE Usage And Synthesis
Uses
4-Nitrophenyl α-L-Rhamnopyranoside is a chromogenic substrate for naringinase.
Uses
4-Nitrophenyl α-L-rhamnopyranoside has been used as a substrate to determine β-glucosidase activity. It has also been used as a substrate to measure α-L-rhamnosidase activity of Oenococcus oeni and Aspergillus terreus.
Biochem/physiol Actions
4-Nitrophenyl α-L-rhamnopyranoside is a substrate for determining α-L-rhamnosidase activity. The hydrolysis of 4-Nitrophenyl α-L-rhamnopyranoside by the enzyme yields 4-nitrophenol, measured at 405 nm spectrophotometrically.
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDESupplier
Feiyang Biotechnology Co., Ltd Gold
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- 0533-7866336 13573361699
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- 010-82848833 400-666-7788
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Chemsky(shanghai)International Co.,Ltd.
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- 021-50135380
- shchemsky@sina.com
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P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE(18918-31-5)Related Product Information
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- 4-NITROPHENYL-BETA-D-MANNOPYRANOSIDE
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- CYANIDIN-3-GALACTOSIDE CHLORIDE
- 4-NITROPHENYL-BETA-D-CELLOBIOSIDE
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- P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE