Interesting facts
Interesting Facts about 4-Methyl-3,5-dinitro-aniline
4-Methyl-3,5-dinitro-aniline is a fascinating compound that showcases a rich interplay between chemistry and applications in various fields. Here are some key points:
- Chemical Structure: This compound belongs to the family of aniline derivatives, characterized by the presence of amino (-NH2) and nitro (-NO2) groups. The presence of multiple nitro groups indicates its potential as a powerful explosive or dye precursor.
- Applications: 4-Methyl-3,5-dinitro-aniline plays a significant role in the production of dyes, particularly in the textile industry. Its vibrant colors are extensively used to produce a variety of shades.
- Explosive Properties: Due to its nitro groups, this compound has notable explosive properties, making it relevant in the field of propellants and explosives. Known as a secondary explosive, it requires a detonator to explode but can be extremely powerful.
- Research Significance: Scientists often explore compounds like 4-Methyl-3,5-dinitro-aniline to understand their stability, reactivity, and decomposition pathways. Such studies can yield important insights into safety measures associated with handling energetic materials.
- Environmental Considerations: As a synthetic chemical, awareness regarding the environmental impact of 4-Methyl-3,5-dinitro-aniline is crucial. Its potential toxicity and effects on ecosystems necessitate careful monitoring and regulations in its production and disposal.
In summary, 4-Methyl-3,5-dinitro-aniline is not just a chemical compound; it embodies the intersection of industrial utility and environmental responsibility. As research continues, it will be intriguing to see how this compound evolves within both the scientific community and commercial applications.
Synonyms
4-Amino-2,6-dinitrotoluene
4-Methyl-3,5-dinitroaniline
19406-51-0
3,5-Dinitro-4-methylaniline
3,5-Dinitro-p-toluidine
2,6-Dinitro-4-aminotoluene
p-Toluidine, 3,5-dinitro-
4-METHYL-3,5-DINITROBENZENAMINE
4-Adnt
Benzenamine, 4-methyl-3,5-dinitro-
NSC 25010
VGF967AJX2
NSC-25010
NSC-55353
DTXSID8074312
CHEBI:77424
1-AMINO-3,5-DINITRO-4-METHYLBENZENE
DTXCID8036077
RefChem:517563
153919-64-3
4-methyl-3,5-dinitro-aniline
4-Methyl-3,5-dinitrophenylamine
MFCD00033978
4-methyl-3,5-dinitro-phenylamine
4-Amino-1-methyl-2,6-dinitrobenzene
Benzenamine,5-dinitro-
p-Toluidine,5-dinitro-
58449-89-1
CCRIS 5190
Benzenamine, 3,5-dinitro-4-methyl-
BRN 2462150
AI3-23207
4-Toluenamine, 2,6-dinitro-
UNII-VGF967AJX2
SCHEMBL314000
SCHEMBL2228406
4-Methyl-3,5-dinitroaniline #
(4-methyl-3,5-dinitrophenyl)amine
NSC25010
NSC55353
BBL023069
SBB002337
STK313330
AKOS000310028
AC-10512
SY080845
VS-07320
DB-006623
ST4104985
CS-0237441
NS00003369
EN300-183718
G67756
A813697
Q27105069
4-Amino-2,6-dinitrotoluene, vial of 100 mg, analytical standard
Solubility of 4-methyl-3,5-dinitro-aniline
4-methyl-3,5-dinitro-aniline, a substituted aromatic amine, exhibits specific solubility characteristics that are important to understand for its applications. The solubility of this compound can be influenced by several factors, including:
However, it is crucial to note that:
In summary, while 4-methyl-3,5-dinitro-aniline has characteristics that promote solubility in polar solvents, its overall solubility profile is somewhat limited in non-polar solvents and water. Understanding these solubility properties is crucial for effectively utilizing this compound in various chemical processes.