Basic information Safety Supplier Related

5-Hydroxy-2-nitrobenzoic acid

Basic information Safety Supplier Related

5-Hydroxy-2-nitrobenzoic acid Basic information

Product Name:
5-Hydroxy-2-nitrobenzoic acid
Synonyms:
  • 5-hydroxy-2-nitro-benzoicaci
  • RARECHEM AL BE 0679
  • 3-carboxy-4-nitrophenol
  • 5-Hydroxy-2-nitrobenzoic acid, tech
  • 2-Nitro-5-hydroxybenzoic acid
  • 5-HYDROXY-2-NITROBENZOIC ACID
  • 5-hydroxy-2-nitrobenzoic acid(SALTDATA: FREE)
  • 5-Hydroxy-2-nitrobenzoic
CAS:
610-37-7
MF:
C7H5NO5
MW:
183.12
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Carboxylic Acids
  • Phenyls & Phenyl-Het
  • Carboxylic Acids
  • Phenyls & Phenyl-Het
Mol File:
610-37-7.mol
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5-Hydroxy-2-nitrobenzoic acid Chemical Properties

Melting point:
170-171°C
Boiling point:
455.0±40.0 °C(Predicted)
Density 
1.631
RTECS 
DH2528250
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
2.06±0.25(Predicted)
color 
White to Yellow to Green
CAS DataBase Reference
610-37-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
Hazard Note 
Irritant
HS Code 
29163990
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5-Hydroxy-2-nitrobenzoic acid Usage And Synthesis

Uses

5-Hydroxy-2-nitrobenzoic acid inhibits the activity of wild type-bovine low Mr protein tyrosine phosphatase. The inhibition constant has been evaluated.

Synthesis

2516-95-2

610-37-7

General procedure for the synthesis of 2-nitro-5-hydroxybenzoic acid from 5-chloro-2-nitrobenzoic acid: 5-chloro-2-nitrobenzoic acid (32.00 g, 0.159 mol) was dissolved in 15% aqueous sodium hydroxide solution and reacted at reflux under nitrogen protection for 72 hours. After completion of the reaction, the pH of the reaction solution was adjusted to 1.0 with dilute hydrochloric acid and then extracted with ethyl acetate. The ethyl acetate extracts were combined and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to give 28.05 g of 2-nitro-5-hydroxybenzoic acid in 96.5% yield.

References

[1] Chemistry - A European Journal, 2013, vol. 19, # 43, p. 14654 - 14664
[2] Patent: CN106478548, 2017, A. Location in patent: Paragraph 0019-0020; 0035-0036; 0051-0052; 0067-0068
[3] Patent: US2017/158680, 2017, A1. Location in patent: Paragraph 0330; 0331; 0332
[4] Patent: WO2003/97641, 2003, A2. Location in patent: Page/Page column 63
[5] Patent: US4348396, 1982, A

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