4-aminophenyl α-d-mannopyranoside
P-AMINOPHENYL ALPHA-D-MANNOPYRANOSIDE
CAS: 34213-86-0
Molecular Formula: C12H17NO6
4-aminophenyl α-d-mannopyranoside - Names and Identifiers
4-aminophenyl α-d-mannopyranoside - Physico-chemical Properties
| Molecular Formula | C12H17NO6 |
| Molar Mass | 271.27 |
| Density | 1.517±0.06 g/cm3(Predicted) |
| Melting Point | 165-166°C |
| Boling Point | 555.9±50.0 °C(Predicted) |
| Water Solubility | H2O: soluble |
| Appearance | Morphological Solid color Off-White to Beige |
| pKa | 12.93±0.70(Predicted) |
| Storage Condition | 2-8°C |
| Stability | Hygroscopic |
| MDL | MFCD00067366 |
| Use | 4-Aminophenyl-ALPHA-D-mannosidase is the substrate of mannosidase. As a rapid molecular diagnostic method, the absorbance of p-nitrophenol produced by hydrolysis of 4-aminophenyl-ALPHA-D-mannosidase by the enzyme is detected by spectrophotometry, and its enzymatic activity is confirmed. Determine whether there is an increase or decrease in the activity of mannosidase and whether there is a deletion of the enzyme. |
4-aminophenyl α-d-mannopyranoside - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29400090 |
4-aminophenyl α-d-mannopyranoside - Upstream Downstream Industry
| Raw Materials | 4-Isothiocyanatophenyl α-D-mannopyranoside |
4-aminophenyl α-d-mannopyranoside - Introduction
4-aminophenyl-α-d-mannopyranoside is an organic compound with the chemical formula C13H19NO6. It is a compound containing amino and glycosidic groups and has a sweet taste.
P-Aminophenyl-α-D-mannopyranoside has a variety of applications in the biological field. It can be used as a substrate or reagent of glycosidase for studying the catalytic mechanism of glycosidase and sugar metabolism. In addition, it can also be used for the preparation of drugs, antibiotics, carbohydrate content analysis and biochemical experiments in the staining.
The common method for preparing P-aminophenyl-α-D-mannopyranoside is synthesis by chemical reaction. A common synthetic method is to react aniline with α-D-pyranoside to give the desired product.
For safety information, P-aminophenyl-α-D-mannopyranoside is relatively safe under regular experimental conditions. However, basic laboratory safety measures are still required to avoid contact with skin and eyes, inhalation and swallowing. When handling it, wear appropriate protective gloves and eye protection equipment, and maintain good ventilation conditions. If necessary, consult a chemical expert or refer to specialized chemical literature to ensure the correct and safe use of the compound.
P-Aminophenyl-α-D-mannopyranoside has a variety of applications in the biological field. It can be used as a substrate or reagent of glycosidase for studying the catalytic mechanism of glycosidase and sugar metabolism. In addition, it can also be used for the preparation of drugs, antibiotics, carbohydrate content analysis and biochemical experiments in the staining.
The common method for preparing P-aminophenyl-α-D-mannopyranoside is synthesis by chemical reaction. A common synthetic method is to react aniline with α-D-pyranoside to give the desired product.
For safety information, P-aminophenyl-α-D-mannopyranoside is relatively safe under regular experimental conditions. However, basic laboratory safety measures are still required to avoid contact with skin and eyes, inhalation and swallowing. When handling it, wear appropriate protective gloves and eye protection equipment, and maintain good ventilation conditions. If necessary, consult a chemical expert or refer to specialized chemical literature to ensure the correct and safe use of the compound.
Last Update：2024-04-09 20:45:29
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Product Name: 4-Aminophenyl α-D-mannopyranoside Visit Supplier Webpage Request for quotationCAS: 34213-86-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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Raw Materials for 4-aminophenyl α-d-mannopyranoside