Basic information Safety Supplier Related

2-(2,4-Dinitrobenzyl)pyridine

Basic information Safety Supplier Related

2-(2,4-Dinitrobenzyl)pyridine Basic information

Product Name:
2-(2,4-Dinitrobenzyl)pyridine
Synonyms:
  • 2-[(2,4-dinitrophenyl)methyl]-pyridin
  • TIMTEC-BB SBB003093
  • 2-(2,4-DINITROBENZYL)PYRIDINE
  • 2-(2,4-BISNITROBENZYL)PYRIDINE
  • 2-[(2,4-dinitrophenyl)methyl]pyridine
  • 2-(2,4-Dinitrobenzyl)pyridine,99%
  • AKOS 92219
  • Pyridine, 2-[(2,4-dinitrophenyl)Methyl]-
CAS:
1151-97-9
MF:
C12H9N3O4
MW:
259.22
EINECS:
214-567-9
Mol File:
1151-97-9.mol
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2-(2,4-Dinitrobenzyl)pyridine Chemical Properties

Melting point:
92-94°C
Boiling point:
402.47°C (rough estimate)
Density 
1.3450 (rough estimate)
refractive index 
1.5700 (estimate)
form 
powder to crystal
pka
4.42±0.12(Predicted)
color 
White to Yellow to Green
BRN 
265115
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference
1151-97-9(CAS DataBase Reference)
EPA Substance Registry System
Pyridine, 2-[(2,4-dinitrophenyl)methyl]- (1151-97-9)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
TSCA 
Yes
HS Code 
2933.39.9200

MSDS

  • Language:English Provider:ALFA
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2-(2,4-Dinitrobenzyl)pyridine Usage And Synthesis

Chemical Properties

White to Yellow to Green powder to crystal.

Uses

2-(2,4-Dinitrobenzyl)pyridine can be used in organic synthesis and pharmaceutical intermediates.

Preparation

Synthesis of 2-(2,4-Dinitrobenzyl)pyridine
A solution of sulfuric acid (15 mL) is placed in an ice bath along with a magnetic stirrer.Benzylpyridine (2.4 mL) is added dropwise, maintaining a temperature below 10°C. This process is then repeated for fuming nitric acid (3.0 mL), once again maintaining the temperature. After addition mixture is allowed to stand at room temperature for 30minutes. Once completed reaction mixture is heated in an 80°C water bath for 20 minutes. Mixture is then poured into a conical flask containing crushed ice (50 cm3) which is stirred in an ice bath. Using a separating funnel aqueous ammonia is added (50 – 100 mL) until the pH rises to ~9 – 10 and filter using a Buchner funnel. Ethyl acetate (40mL) & sodium hydroxide (40mL) is added to the solid and stirred using a magnetic stirrer until dissolved.
Dry the organic layer using magnesium sulfate as the drying agent which is then followed by a rotary evaporator (40°C, vacuum). Product is then washed using cold methylated spirit and left to recrystalise.

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