Identification | More | [Name]
4-NITROPICOLINIC ACID | [CAS]
13509-19-8 | [Synonyms]
4-NITROPICOLINIC ACID 4-NITROPYRIDINE-2-CARBOXYLIC ACID RARECHEM AL BO 0806 4-Nitro-2-pyridinecarboxylic acid Nitropicolinicacid 2-Pyridinecarboxylic acid, 4-nitro- 4-NITROPICOLINIC ACID 98+% 16367 4-NITRO-PYRIDINE-2-CARBOXYLIC ACID 4-Nitropicolinic acid ,97% | [EINECS(EC#)]
678-295-6 | [Molecular Formula]
C6H4N2O4 | [MDL Number]
MFCD00191562 | [Molecular Weight]
168.11 | [MOL File]
13509-19-8.mol |
Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [HS Code ]
29339900 |
Hazard Information | Back Directory | [Chemical Properties]
White solid | [Synthesis]
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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