Interesting facts
Interesting Facts about 3-Nitroaniline
3-Nitroaniline is an intriguing compound with a rich history in chemistry and industry. Here are some notable facts:
- Chemical Structure: This compound consists of an aniline backbone, which is an aromatic amine, modified by a nitro group at the meta position. This molecular arrangement impacts its reactivity and properties significantly.
- Applications: 3-Nitroaniline is extensively used in the production of dyes and other organic compounds. It serves as an important intermediate in the manufacture of azo dyes, which are widely used in textiles.
- Synthesis: The synthesis of 3-nitroaniline typically involves the nitration of aniline. This reaction requires careful control of conditions since the presence of multiple amino groups can lead to a mixture of products.
- Biological Significance: Research has shown that nitroanilines can have biological activity. 3-Nitroaniline has been studied for its potential antimicrobial properties, making it a subject of interest in medicinal chemistry.
- Environmental Concerns: Due to its use in the dye industry, 3-nitroaniline has been found in environmental samples. It is essential to monitor its presence as it can be toxic and has implications for aquatic life.
- Safety Precautions: Like many nitro compounds, 3-nitroaniline can be hazardous. It is essential to handle it with care in a laboratory setting, following proper safety protocols to avoid exposure or environmental contamination.
The study of 3-nitroaniline not only enhances our understanding of chemical reactions but also paves the way for future innovations in materials science and medicinal applications. As researchers continue to explore its properties and possibilities, exciting developments are sure to arise!
Synonyms
3-Nitroaniline
99-09-2
M-NITROANILINE
Benzenamine, 3-nitro-
3-Nitrobenzenamine
Nitranilin
3-Nitrophenylamine
3-Aminonitrobenzene
m-Nitraniline
Fast Orange Base R
Devol Orange R
Azobase MNA
m-Nitrophenylamine
m-Aminonitrobenzene
m-Nitroaminobenzene
Aniline, m-nitro-
1-Amino-3-nitrobenzene
Fast Orange M Base
Fast Orange R Base
Fast Orange R Salt
Orange Base Irga I
Daito Orange Base R
Diazo Fast Orange R
Fast Orange MM Base
Naphtoelan Orange R Base
Amarthol Fast Orange R Base
Hiltonil Fast Orange R Base
C.I. Azoic Diazo Component 7
3-Nitro-phenylamine
NSC 9574
CI Azoic Diazo Component 7
C.I. 37030
CCRIS 2318
3-NITRO-ANILINE
HSDB 2570
EINECS 202-729-1
MFCD00007782
Aniline, 3-nitro-
CM50SM561T
CI 37030
DTXSID6025725
AI3-52474
NSC-9574
NITROANILINE, M-
M-NITROANILINE [MI]
3-NITROANILINE [HSDB]
DTXCID505725
meta-Nitroaniline
Nitroaniline, 3-
SMR000343223
UNII-CM50SM561T
mNitraniline
mNitroaniline
3nitroaniline
m-nitro aniline
m-nitro-aniline
mNitrophenylamine
Aniline, mnitro
3Nitrobenzenamine
3Nitrophenylamine
3-nitro aniline
mAminonitrobenzene
mNitroaminobenzene
3Aminonitrobenzene
1Amino3nitrobenzene
3-Nitrobenzeneamine
3-NA, aniline
Benzenamine, 3nitro
(3-nitrophenyl)-amine
3-Nitroaniline, 98%
3-Nitroaniline, 99%
WLN: ZR CNW
ORANGE BASE IRGA 1
SCHEMBL1487
ghl.PD_Mitscher_leg0.915
MLS000517063
MLS002415745
UN 1661 (Salt/Mix)
CHEMBL14068
SCHEMBL12707526
NSC9574
HMS2666G03
3-Nitroaniline, analytical standard
STR01954
Tox21_200386
STL137655
AKOS000119115
m-Nitroaniline [UN1661] [Poison]
CAS-99-09-2
NCGC00091126-01
NCGC00091126-02
NCGC00257940-01
DB-057758
N0117
NS00006068
EN300-17396
D97675
AC-907/25014117
Q2668442
Z56924547
202-729-1
Solubility of 3-nitroaniline
3-nitroaniline, with the chemical formula C6H6N2O2, is known for its distinctive solubility characteristics in various solvents. Its solubility can be summarized with the following points:
Overall, the solubility properties of 3-nitroaniline reflect a balance between its structural characteristics and the nature of the solvent, highlighting the importance of both polarity and intermolecular interactions in determining solubility.