2-Amino-3-pyridinol

Names

[ Name ]:
2-Amino-3-pyridinol

[Synonym ]:
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

Biological Activity

[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]:

Research Areas >> Others

[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。

Chemical & Physical Properties

[ 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.

MSDS

Click to get detail MSDS

Safety Information

[ 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

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ 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%

Articles

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)

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)

Vinyltriphenylphosphonium salt mediated synthesis of 1, 4-benzoxazine and coumarin derivatives. Yavari I, et al.

Tetrahedron 58(34) , 6895-6899, (2002)