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13509-19-8

13509-19-8 Structure

13509-19-8 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[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
[Detection Methods]

HPLC
[CAS DataBase Reference]

13509-19-8(CAS DataBase Reference)
Safety DataBack 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
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sulfuric acid-->Acetic acid-->Nitric acid-->Chloroform-->Ammonium hydroxide-->Hydrogen peroxide-->Potassium permanganate-->Phosphorus trichloride-->Chromium(VI) oxide-->2-Picoline-->2-Cyano-4-nitropyridine-->2-Methyl-4-nitropyridine-->4-Nitropyridine N-oxide-->4-Amino-2-picoline-->Pyridine-N-oxide
[Preparation Products]

4-Methoxypyridine-2-carboxylic acid
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

2-CYANO-4-NITROPYRIDINE

19235-88-2

4-NITROPICOLINIC ACID

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
Spectrum DetailBack Directory
[Spectrum Detail]

4-NITROPICOLINIC ACID(13509-19-8)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

4-Nitropicolinic Acid,>98.0%(T)(13509-19-8)
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