3-HYDROXY-4-NITROBENZOIC ACID

Names

[ CAS No. ]:
619-14-7

[ Name ]:
3-HYDROXY-4-NITROBENZOIC ACID

[Synonym ]:
RARECHEM AL BE 0673
3-Hydroxyl-4-nitrobenzoic
Benzoic acid, 3-hydroxy-4-nitro-
EINECS 210-580-9
3-HYDROXYL-4-NITROBENZOIC ACID
4-nitro-3-hydroxy-benzoic acid
3-Hydroxy-4-nitro-benzoesaeure
3-hydroxy-4-nitro-benzoic acid
Benzoic acid,3-hydroxy-4-nitro
MFCD00007110
5-carboxy-2-nitrophenol
3-Hydroxy-4-nitrobenzoic acid

Biological Activity

[Description]:

3-Hydroxy-4-nitrobenzoic 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]:
1.6±0.1 g/cm3

[ Boiling Point ]:
381.0±32.0 °C at 760 mmHg

[ Melting Point ]:
229-231 °C(lit.)

[ Molecular Formula ]:
C₇H₅NO₅

[ Molecular Weight ]:
183.12

[ Flash Point ]:
175.4±13.6 °C

[ Exact Mass ]:
183.016769

[ PSA ]:
103.35000

[ LogP ]:
1.99

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

[ Index of Refraction ]:
1.664

[ Water Solubility ]:
insoluble

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 ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29182990

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2918290000

[ Summary ]:
HS: 2918290000 other carboxylic acids with phenol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) VAT:17.0% MFN tariff:6.5% General tariff:30.0%

Articles

Inhibitory Effects of Conjugated Epicatechin Metabolites on Peroxynitrite-mediated Nitrotyrosine Formation.

J. Clin. Biochem. Nutr. 42 , 50-3, (2008)

Previously, we identified four metabolites of (-)-epicatechin in blood and urine: (-)-epicatechin-3'-O-glucuronide (E3'G), 4'-O-methyl-(-)-epicatechin-3'-O-glucuronide (4'ME3'G), (-)-epicatechin-7-O-g...