Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Hydroxypyridine >  6-Hydroxy-5-nitro-2-picoline

6-Hydroxy-5-nitro-2-picoline

Basic information Safety Supplier Related

6-Hydroxy-5-nitro-2-picoline Basic information

Product Name:
6-Hydroxy-5-nitro-2-picoline
Synonyms:
  • HYDROXY-6-METHYL-3-NITROPYRIDINE
  • 6-METHYL-3-NITRO-2(1H)-PYRIDINONE
  • 6-METHYL-3-NITRO-PYRIDIN-2-OL
  • 6-HYDROXY-5-NITRO-2-PICOLINE
  • 3-NITRO-6-METHYLPYRIDIN-2-OL
  • 2-HYDROXY-6-METHYL-3-NITROPYRIDINE
  • 2-HYDROXY-3-NITRO-6-METHYLPYRIDINE
  • 2-HYDROXY-3-NITRO-6-PICOLINE
CAS:
39745-39-6
MF:
C6H6N2O3
MW:
154.12
Product Categories:
  • blocks
  • Pyridines
  • Pyridine
  • Pyridines derivates
  • compounds of pyridine
Mol File:
39745-39-6.mol
More
Less

6-Hydroxy-5-nitro-2-picoline Chemical Properties

Melting point:
225-226 C
Boiling point:
277.46°C (rough estimate)
Density 
1.4564 (rough estimate)
refractive index 
1.5100 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
8.47±0.10(Predicted)
color 
Light yellow to Brown to Dark green
CAS DataBase Reference
39745-39-6(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-41-37/38-22
Safety Statements 
37/39-26-36-39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29337900

MSDS

  • Language:English Provider:ACROS
More
Less

6-Hydroxy-5-nitro-2-picoline Usage And Synthesis

Chemical Properties

Yellow crystalline powder

Uses

2-Hydroxy-6-methyl-3-nitropyridine is a water soluble compound that has been used for the treatment of tuberculosis.

Synthesis

21901-29-1

39745-39-6

Synthesis of 2-hydroxy-3-nitro-6-methylpyridine: 2-amino-3-nitro-6-methylpyridine (10 g, 0.065 mol) was added to 100 mL of water, and concentrated sulfuric acid (12 mL) was added slowly under stirring and cooled to 0 °C in an ice bath. Sodium nitrite (6.9 g, 0.098 mol) was added in batches, and the reaction temperature was maintained at 0 °C for 4 h, followed by a 12 h standing time. A large amount of yellow precipitate precipitated during the reaction, the precipitate was collected by filtration under reduced pressure and dried under vacuum to give 7.7 g of yellow target product in 77% yield. The melting point of the product was 216.5-218.5 °C (water).

References

[1] Patent: EP2366691, 2011, A1. Location in patent: Page/Page column 11
[2] Journal of the American Chemical Society, 1952, vol. 74, p. 3828,3830

6-Hydroxy-5-nitro-2-picolineSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
INTATRADE GmbH
Tel
+49 3493/605464
Email
sales@intatrade.de
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com