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4-NITROPICOLINIC ACID

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4-NITROPICOLINIC ACID Basic information

Product Name:
4-NITROPICOLINIC ACID
Synonyms:
  • RARECHEM AL BO 0806
  • 4-NITROPICOLINIC ACID
  • 4-NITROPYRIDINE-2-CARBOXYLIC ACID
  • 4-Nitro-2-pyridinecarboxylic acid
  • Nitropicolinicacid
  • 2-Pyridinecarboxylic acid, 4-nitro-
  • 4-Nitropicolinic acid ,97%
  • 4-NITROPICOLINIC ACID 98+%
CAS:
13509-19-8
MF:
C6H4N2O4
MW:
168.11
EINECS:
678-295-6
Product Categories:
  • Pyridines
Mol File:
13509-19-8.mol
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4-NITROPICOLINIC ACID Chemical Properties

Melting point:
153℃
Boiling point:
384.9±27.0 °C(Predicted)
Density 
1.570
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
2.88±0.10(Predicted)
color 
White to Orange to Green
CAS DataBase Reference
13509-19-8(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
29339900
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4-NITROPICOLINIC ACID Usage And Synthesis

Chemical Properties

White solid

Synthesis

19235-88-2

13509-19-8

Synthesis of III-2-2:4-nitropyridine carboxylic acid 5.00 g (34 mmol) of 2-cyano-4-nitropyridine was dissolved in 50 g of 90% sulfuric acid and the reaction was stirred at 120°C for 2 hours. Subsequently, a solution of 5.60 g of sodium sulfite dissolved in 10 ml of water was slowly added dropwise at 20 °C to 25 °C, and the stirring was continued at the same temperature for 1 h. After that, the reaction was warmed up to 80 °C for 1 h. The reaction was completed by cooling to room temperature. Upon completion of the reaction, it was cooled to room temperature, diluted by adding 100 g of ice water, and the pH of the mixture was adjusted with sodium carbonate to about 2. The mixture was allowed to stand in a refrigerator to induce precipitation of solids. The precipitate was collected by filtration and recrystallized using a water-acetone solvent mixture to give 3.50 g of light yellow crystalline product in 62.1% yield. The melting point of the product was 157°-158°C (accompanied by decomposition).The IR (KBr) spectrum showed characteristic absorption peaks located at 1710, 1600, 1585, 1535 cm-1 .

References

[1] Journal of the American Chemical Society, 2012, vol. 134, # 47, p. 19366 - 19369
[2] Patent: US5219847, 1993, A
[3] Journal of Organometallic Chemistry, 1997, vol. 544, # 2, p. 163 - 174

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