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3,4-Dichloronitrobenzene

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3,4-Dichloronitrobenzene Basic information

Product Name:
3,4-Dichloronitrobenzene
Synonyms:
  • 1-Nitro-3,4-dichlorobenzene
  • 3,4-dichlornitrobenzen
  • 3,4-dichloronitrobenzen(czech)
  • 1,2-dichloro-4-nitro-benzen
  • 3,4-Dichloronitroben
  • 3,4-Dichloronitrobenzene,95%
  • 3,4-Dichlor-1-nitrobenzol
  • 3,4-Dichluoronitrobenzene
CAS:
99-54-7
MF:
C6H3Cl2NO2
MW:
192
EINECS:
202-764-2
Product Categories:
  • Dyestuff Intermediates
  • Aromatic Halides (substituted)
  • Intermediates of Dyes and Pigments
  • Organics
  • Benzene derivates
Mol File:
99-54-7.mol
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3,4-Dichloronitrobenzene Chemical Properties

Melting point:
39-41 °C(lit.)
Boiling point:
255-256 °C(lit.)
Density 
1.48 g/cm3 (55℃)
vapor pressure 
0.01 hPa (20 °C)
refractive index 
1.5929 (estimate)
Flash point:
255 °F
storage temp. 
Store below +30°C.
solubility 
0.151g/l
form 
Crystalline Mass
color 
Yellow to brown
Water Solubility 
151 mg/L (20 ºC)
FreezingPoint 
30~31℃
BRN 
1818163
Stability:
Stable. Incompatible with strong oxidizing agents, strong bases.
CAS DataBase Reference
99-54-7(CAS DataBase Reference)
NIST Chemistry Reference
Benzene, 1,2-dichloro-4-nitro-(99-54-7)
EPA Substance Registry System
3,4-Dichloronitrobenzene (99-54-7)
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
22-36-43-51/53
Safety Statements 
26-36/37-61-39-24/25
RIDADR 
2811
WGK Germany 
3
RTECS 
CZ5250000
Autoignition Temperature
420 °C
TSCA 
Yes
HazardClass 
9
PackingGroup 
III
HS Code 
29049085
Hazardous Substances Data
99-54-7(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 643 mg/kg LD50 dermal Rat > 2000 mg/kg

MSDS

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3,4-Dichloronitrobenzene Usage And Synthesis

Chemical Properties

colourless to yellow crystals or beige powder

Uses

1,2-Dichloro-4-nitrobenzene is an intermediate in the synthesis of agrochemicals. Studies have been conducted to use 1,2-Dichloro-4-nitrobenzene as an organic intermediate for the synthetic preparation of ciprofloxacin (C482500).

Production Methods

Nitration of 1,2-dichlorobenzene with mixed acid at 35 – 60 ℃ results in a mixture of 3-nitro (10 %) and 4-nitro (90 %) isomers, which are separated by crystallization. A more expensive process (two stages from chlorobenzene) is based on chlorination of molten 4-chloronitrobenzene (90 – 100 ℃) by a process similar to that used for 3- chloronitrobenzene production. Chlorination has the advantage of giving a pure product, but it cannot be used if the isomeric 1,2-dichloro-3-nitrobenzene is also required.

Synthesis Reference(s)

The Journal of Organic Chemistry, 42, p. 3494, 1977 DOI: 10.1021/jo00442a009

General Description

Colorless crystals or light beige solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Can react vigorously with oxidizing materials.

Fire Hazard

3,4-Dichloronitrobenzene is combustible.

Flammability and Explosibility

Non flammable

Purification Methods

Crystallise it from absolute EtOH. [Beilstein 5 IV 726.]

3,4-Dichloronitrobenzene Preparation Products And Raw materials

Raw materials

Preparation Products

3,4-DichloronitrobenzeneSupplier

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