Uses
ChemicalBook > CAS DataBase List > 2,4-Dihydroxy-3-nitropyridine

2,4-Dihydroxy-3-nitropyridine

Uses
Product Name
2,4-Dihydroxy-3-nitropyridine
CAS No.
89282-12-2
Chemical Name
2,4-Dihydroxy-3-nitropyridine
Synonyms
3-NITRO-2,4-PYRIDINEDIOL;Dihydroxy-3-nitropyridine;4-Dihydroxy-3-nitropyridine;2,4-Dihyroxy-3-nitropyridine;2,4-Hydroxy-3-nitropyridine.;4-Hydroxy-3-nitro-2-pyridone;2,4-Diydroxy-3-nitropyridine;2,4-DIHYDROXY-3-NITROPYRIDINE;4,6-DIHYDROXY-5-NITRO PYRIDINE;2,4-Dihydroxy-3-nitropyridine-1
CBNumber
CB7405853
Molecular Formula
C5H4N2O4
Formula Weight
156.1
MOL File
89282-12-2.mol
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2,4-Dihydroxy-3-nitropyridine Property

Melting point:
265°C (dec.)
Boiling point:
305.6±42.0 °C(Predicted)
Density 
1.65±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
4.50±1.00(Predicted)
color 
Light yellow to Yellow to Green
BRN 
149558
InChI
InChI=1S/C5H4N2O4/c8-3-1-2-6-5(9)4(3)7(10)11/h1-2H,(H2,6,8,9)
InChIKey
BKYGVGWYPFVKTK-UHFFFAOYSA-N
SMILES
C1(=O)NC=CC(O)=C1[N+]([O-])=O
CAS DataBase Reference
89282-12-2(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37
RIDADR 
3335
HS Code 
29333990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
R436798
Product name
2,4-DIHYDROXY-3-NITROPYRIDINE
Purity
Aldrich<sup>CPR</sup>
Packaging
1 unit
Price
$30.7
Updated
2025/07/31
Sigma-Aldrich
Product number
R436798
Product name
2,4-DIHYDROXY-3-NITROPYRIDINE
Purity
AldrichCPR
Packaging
1G
Price
$29.8
Updated
2024/03/01
TCI Chemical
Product number
D4002
Product name
2,4-Dihydroxy-3-nitropyridine
Purity
>98.0%(GC)
Packaging
5g
Price
$45
Updated
2025/07/31
TCI Chemical
Product number
D4002
Product name
2,4-Dihydroxy-3-nitropyridine
Purity
>98.0%(GC)
Packaging
25g
Price
$133
Updated
2025/07/31
TRC
Product number
B506300
Product name
3-Nitropyridine-2,4-diol
Packaging
10g
Price
$75
Updated
2021/12/16
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2,4-Dihydroxy-3-nitropyridine Chemical Properties,Usage,Production

Uses

2,4-Dihydroxy-3-nitropyridine can be used as a material additive, pharmaceutical chemical, and organic synthesis intermediate. During synthetic transformation, the hydroxyl groups in the structure can be easily converted into halogen atoms due to the influence of the pyridine ring and nitro group. It should be noted that by changing the reaction conditions, one of the two hydroxyl groups can be selectively halogenated, or both can be converted simultaneously. Furthermore, under acidic conditions, a bromine atom can be introduced at the 5-position of the pyridine using liquid bromine.

Chemical Properties

Yellow powder

Reactions

2,4-Dihydroxy-3-nitropyridine could be quickly transformed into 5-bromo-2,4-dihydroxy-3-nitropyridine by the action of a solution of bromine. 3.5 g of 2,4-Dihydroxy-3-nitropyridine were heated with a mixture of 1.15 ml of bromine and 30 ml of acetic acid at 70℃ for 15 minutes. When the reaction mixture was cooled with ice, 3.7 g of 5-bromo-2,4-dihydroxy-3-nitropyridine separated out[1]. Yield: 70 %

Synthesis

626-03-9

89282-12-2

Step 59a. Synthesis of 2,4-dihydroxy-3-nitropyridine (compound 0108): fuming nitric acid (90 mL) was slowly added to a stirring solution of 2,4-dihydroxypyridine (0601) (100 g, 0.9 mol) dissolved in ethyl acetate (300 mL) at 0 °C. After 45 minutes of reaction, the reaction solution was carefully poured into crushed ice and the mixture was cooled in a refrigerator. The resulting precipitate was collected by filtration, washed with cold water and dried to give 4-hydroxy-3-nitropyridin-2(1H)-one (0108) (135 g, 96% yield) as a light yellow solid.LCMS: 157 [M + 1]+; 1H NMR (DMSO-d6) δ 6.05 (d, 1H, J = 7.2 Hz), 7.47 (d, 1H, J = 7.2 Hz), 11.91 (s, 1H), 12.47 (s, 1H).

References

[1] Kolder, C. R. , and H. J. D. Hertog . Migration of halogen atoms in halogeno-derivatives of 2,4-dihydroxypyridine (II). Recueil des Travaux Chimiques des Pays-Bas 72.10(2010):853-858.

2,4-Dihydroxy-3-nitropyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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2,4-Dihydroxy-3-nitropyridine Suppliers

TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
Fine Corporation
Tel
--
Fax
--
Email
info@fine-c.jp
Country
Japan
ProdList
1427
Advantage
58
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View Lastest Price from 2,4-Dihydroxy-3-nitropyridine manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
2,4-Dihydroxy-3-nitropyridine 89282-12-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-27
Dideu Industries Group Limited
Product
2,4-Dihydroxy-3-nitropyridine 89282-12-2
Price
US $1.10/g
Min. Order
1g
Purity
99.00%
Supply Ability
100 Tons Min
Release date
2021-09-24
Career Henan Chemical Co
Product
2,4-Dihydroxy-3-nitropyridine 89282-12-2
Price
US $1.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
Customized
Release date
2018-12-22

89282-12-2, 2,4-Dihydroxy-3-nitropyridineRelated Search:


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  • Pyridine Series
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