m-BROMONITROBENZENE
|
PRODUCT
IDENTIFICATION
|
CAS
NO. |
585-79-5 |
|
EINECS NO. |
209-563-9 |
FORMULA |
C6H4BrNO2 |
MOL
WT. |
202.01 |
H.S.
CODE
|
2904.90 |
TOXICITY
|
|
SYNONYMS |
3-Bromo-1-nitrobenzene;
|
3-Bromonitrobenzene; 3-Nitrobromobenzene;
1-Bromo-3-nitrobenzene;
|
SMILES |
|
CLASSIFICATION
|
|
PHYSICAL AND CHEMICAL PROPERTIES
|
PHYSICAL
STATE |
yellow
crystalline powder |
MELTING POINT |
53
- 56 C |
BOILING
POINT |
256
C |
SPECIFIC GRAVITY |
1.70
- 1.71 |
SOLUBILITY
IN WATER |
insoluble |
pH |
|
VAPOR DENSITY |
|
AUTOIGNITION
|
|
NFPA
RATINGS
|
Health: 2; Flammability: 1; Reactivity: 0 |
REFRACTIVE
INDEX
|
|
FLASH
POINT |
112
C |
STABILITY |
Stable
under ordinary conditions |
APPLICATIONS
|
The prefix nitro- indicates the presence of NO2- radical, while nitrate refers
to any salt or ester of nitric acid or the NO3- anion. Nitroso- is the prefix
indicating presence of the group -NO and azo- is for -N=N- group. Some range of
organic compounds containing nitrogen include nitro compounds (RNO2 ), nitroso
compounds (RNO), amines (R3N ), amino acids, and natural alkaloids or
nucleotides. The nitrogen ion in nitro compounds is trigonally planar with 120°
angles. There are two resonance bonds so that the two oxygens are equivalent.
Nitro compounds are strongly basic due to electron withdrawing both inductively
and mesomerically. Historically, they
are abundant in dyes and explosives. Nitro compounds, organic hydrocarbons having one or more NO2
groups bonded via nitrogen to the carbon framework, are versatile intermediate
in organic synthesis.
- Michael
addition
- Reduction
- Henry
Reaction (Nitro-aldol reaction)
- Nef
reaction
- O-Alkylation
- Cycloaddition
- Substitution, Elimination, Conversion
reaction
- Alkylation,
Acylation, and Halogenation
m-Bromonitrobenzene
is used as an intermediate for pharmaceuticals
and other organic compounds
|
SALES
SPECIFICATION |
APPEARANCE
|
yellow
crystalline powder |
ASSAY
|
99.0%
min
|
MELTING
POINT
|
53
- 56 C |
TRANSPORTATION |
PACKING |
25kgs
in fiber drum |
HAZARD CLASS |
|
UN
NO. |
|
OTHER
INFORMATION |
Hazard
Symbols: T, Risk Phrases: 23/24/25/33, Safety Phrases: 28A/37/45 |
GENERAL
DESCRIPTION OF NITROBENZENE
|
Nitrobenzene
(also called nitrobenzol ) is a colourless to pale yellow, oily,
highly toxic liquid with the odour of bitter almonds. Nitrobenzene
is manufactured commercially by nitration of benzene (also a common air
pollutant) using a mixture of nitric and sulfuric acids. Commercially
nitrobenzene can be either produced in a batch or by a continuous process. Both
batch and continuous processes employing mixed nitric and sulfuric acids are
used to make nitrobenzene. The continuous process is favored
over the batch process because its production capacity is much larger, it has
lower capital costs and it entails more efficient labor usage. Reactors for the
continuous process also usually utilized lower nitric acid concentrations, are
smaller with more rapid and efficient mixing, and therefore have higher
reaction rates. Nitrobenzene undergoes nitration, halogenation, and
sulfonation much more slowly than does benzene. It may be reduced to a variety
of compounds, depending on the reaction conditions. Most nitrobenzene produced
is reduced to aniline; smaller amounts are converted to azobenzene,
hydrazobenzene (the intermediate for benzidine), and phenylhydroxylamine.
Reduction of both the nitro group and the benzene ring affords cyclohexylamine.
Nitrobenzene is used as a mild oxidizing agent in the syntheses of quinoline
and fuchsin. Nitrobenzene
is used to produce lubricating oils such as those used in motors and
machinery. Nitrobenzene and its derivatives are used in the manufacture
of dyes, drugs, pesticides, polisher, paint, and synthetic rubber.
|
|