Interesting facts
Interesting Facts About 3-Phenylaniline
3-Phenylaniline, also known as m-phenylaniline, is an organic compound that plays a significant role in various fields of chemistry and industry. Here are some fascinating aspects of this compound:
- Structure and Isomerism: 3-Phenylaniline is an aromatic amine, featuring a phenyl group attached to the nitrogen of an aniline. It is one of three isomers of phenylamine, the other two being o-phenylaniline and p-phenylaniline. The subtle differences in positioning can lead to notable changes in properties and reactivity.
- Applications: This compound is highly valuable in the production of dyes and pigments. Its reactivity allows it to serve as a building block for various chemical syntheses. The use of 3-phenylaniline extends to the formulation of antioxidants and stabilizers in plastics.
- Biological Relevance: Some studies suggest that compounds similar to 3-phenylaniline may exhibit biological activity. Although not extensively studied for therapeutic use, understanding its interactions with biological systems could illuminate new pathways for drug development.
- Hazards and Safety: It is essential to handle 3-phenylaniline with caution. Like many aromatic amines, it can be a potential carcinogen and may pose health risks if not managed properly. Adhering to safety protocols is critical in laboratory and industrial settings.
- Historical Context: The study of phenylamines dates back to the 19th century when the importance of aryl amines in dyes was first recognized. The exploration of 3-phenylaniline has contributed to the growth of organic chemistry as a discipline.
In conclusion, 3-phenylaniline is not just a simple compound; it is a cornerstone of various chemical pathways and applications. Understanding its characteristics helps scientists develop safer products and expand our knowledge of organic chemistry.
Synonyms
3-Aminobiphenyl
2243-47-2
m-Aminobiphenyl
3-BIPHENYLAMINE
m-Phenylaniline
CCRIS 2820
BRN 2206824
P632PQP3U1
DTXSID2036825
3-AMINO-1,1'-BIPHENYL
4-12-00-03238 (Beilstein Handbook Reference)
(1,1'-BIPHENYL-3-YL)AMINE
DTXCID0016825
675-679-5
3-Phenylaniline
[1,1'-Biphenyl]-3-amine
biphenyl-3-amine
biphenyl-3-ylamine
3-Aminodiphenyl
(1,1'-Biphenyl)-3-amine
MFCD00047846
CHEMBL1642684
41674-04-8
3-amino biphenyl
UNII-P632PQP3U1
(1,1'-BIPHENYL)AMINE
3-amino-biphenyl
3-phenyl aniline
biphenyl-3-yl-amine
biphenyl, 3-amino-
3-Aminobiphenyl, 97%
17?-Methyl Testosterone
1,1'-biphenyl-3-amine
SCHEMBL173011
QSPL 063
MUNOBADFTHUUFG-UHFFFAOYSA-
BDBM50334283
AKOS002678495
CS-W008030
FA17698
AS-17951
SY032951
DB-006343
B0987
NS00123593
EN300-72523
Q27286270
m-Phenylaniline;3-Aminobiphenyl;3-Amino-1,1'-biphenyl
Z732776406
InChI=1/C12H11N/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H,13H2
Solubility of 3-phenylaniline
3-phenylaniline, known for its aromatic structure, exhibits specific solubility characteristics that are important in various applications. The solubility of a compound in different solvents can depend on several factors including its molecular structure, functional groups, and temperature. In the case of 3-phenylaniline, consider the following:
In summary, the solubility of 3-phenylaniline is influenced by solvent choice and temperature, making it a versatile compound in chemical processes. As noted, "the nature of the solvent is key to determining solubility." Understanding these aspects is essential for manipulating its use in various applications.