4-Amino-3-hydroxybenzoic acid

Names

[ Name ]:
4-Amino-3-hydroxybenzoic acid

[Synonym ]:
4-Amino-3-hydroxy benzoic acid
2-hydroxyaniline
Benzoic acid, 4-amino-3-hydroxy-
2-Amino-5-carboxyphenol
4-Amino-3-hydroxybenzoic acid
MFCD00017094
3-hydroxy-4-aminobenzoate
2hdr
2-hydroxy-4-carboxyaniline
3-hydroxy-4-amino-benzoic acid

Biological Activity

[Description]:

4-Amino-3-hydroxybenzoic Acid 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

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
385.7±37.0 °C at 760 mmHg

[ Melting Point ]:
211-215 °C(lit.)

[ Molecular Formula ]:
C₇H₇NO₃

[ Molecular Weight ]:
153.14

[ Flash Point ]:
187.1±26.5 °C

[ Exact Mass ]:
153.042587

[ PSA ]:
83.55000

[ LogP ]:
0.68

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.691

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922509090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.

Bioorg. Med. Chem. 15 , 2006-15, (2007)

Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-q...

Deconstructing fragment-based inhibitor discovery.

Nat. Chem. Biol. 2 , 720-3, (2006)

Fragment-based screens test multiple low-molecular weight molecules for binding to a target. Fragments often bind with low affinities but typically have better ligand efficiencies (DeltaG(bind)/heavy ...