2-Amino-3-pyridinol structure
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Common Name | 2-Amino-3-pyridinol | ||
|---|---|---|---|---|
| CAS Number | 16867-03-1 | Molecular Weight | 110.11 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 385.2±27.0 °C at 760 mmHg | |
| Molecular Formula | C5H6N2O | Melting Point | 168-172 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 186.8±23.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 2-Amino-3-pyridinol2-Amino-3-hydroxypyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | 2-Amino-3-hydroxypyridine |
|---|---|
| Synonym | More Synonyms |
| Description | 2-Amino-3-hydroxypyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog | |
| In Vitro | 2-氨基-3-羟基吡啶作为分光光度法测定锇的显色试剂。 |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 385.2±27.0 °C at 760 mmHg |
| Melting Point | 168-172 °C(lit.) |
| Molecular Formula | C5H6N2O |
| Molecular Weight | 110.11 |
| Flash Point | 186.8±23.7 °C |
| Exact Mass | 110.048012 |
| PSA | 59.14000 |
| LogP | 0.77 |
| Vapour Pressure | 0.0±0.9 mmHg at 25°C |
| Index of Refraction | 1.651 |
| Storage condition | Room temperature. |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | T:Toxic |
| Risk Phrases | R25;R36/37/38 |
| Safety Phrases | S26-S45-S37/39-S28A |
| RIDADR | UN2811 |
| WGK Germany | 3 |
| Packaging Group | III |
| Hazard Class | 6.1 |
| HS Code | 2933399090 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Synthesis and characterization of some transition metal complexes of 2-amino-3-hydroxypyridine and its application in corrosion inhibition. Mostafa SI and El-Maksoud SA.
Monatsh. Chem 129(5) , 455-466, (1998)
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1 H NMR, IR and UV/VIS Spectroscopic Studies of Some Schiff Bases Derived From 2-Aminobenzothiazole and 2-Amino-3-hydroxypyridine. Issa RM, et al.
J. Chin. Chem. Soc. 55(4) , 875-884, (2008)
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Vinyltriphenylphosphonium salt mediated synthesis of 1, 4-benzoxazine and coumarin derivatives. Yavari I, et al.
Tetrahedron 58(34) , 6895-6899, (2002)
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| 3-Pyridinol, 2-amino- |
| 2-amino-3-hydroxylpyridine |
| 2-AMINO-3-HYDROXYPYRIDIN |
| amino-hydroxypyridine |
| 2-Amino-3-hydroxypyridine |
| 3-Hydroxy-2-pyridinamine |
| 2-Amino-3-hydroxypyr |
| 2-AMINO-PYRIDIN-3-OL |
| 2-amino-3-pyridino |
| EINECS 240-886-8 |
| 3-PYRIDINOL,2-AMINO |
| 2-Amino-3-hydroxy pyridine |
| 2-Amino-3-pyridinol |
| 2-AMINO-3-PYRIDOL |
| 2-AMINO-3-HYDROXYPYRIDINE,GREY SOLID |
| MFCD00006317 |
| 3-HYDROXY-2-AMINOPYRIDINE |
| 3-hydroxypyridin-2-ylamine |
| 2-aminopyridin-3-ol |