Interesting facts
Exploring 4-Phenylaniline
4-Phenylaniline, also known as para-aminobiphenyl, is a fascinating organic compound that plays a significant role in various chemical applications. Here are some interesting facts about this compound:
- Key Component in Dyes: 4-Phenylaniline is predominantly utilized as an intermediate in the manufacturing of azo dyes, which are widely used in the textile industry. These vibrant colors are crucial for producing beautiful fabrics.
- Role in Organic Synthesis: This compound serves as a versatile building block in organic synthesis, allowing chemists to create myriad complex structures and pharmaceuticals. It is a key player in developing novel compounds with potential therapeutic applications.
- Research & Toxicology: 4-Phenylaniline has raised health concerns due to its classification as a potential carcinogen. Studies have indicated that exposure to this compound can lead to health risks, making it an important subject of research in toxicology.
- Historical Perspective: Interestingly, this compound was once commonly used in the rubber industry as a curing agent. However, due to its toxicological profile, many manufacturers have shifted toward safer alternatives.
As a scientist or student, exploring the multifaceted nature of 4-phenylaniline can lead to a deeper understanding of both its valuable industrial applications and health implications. It serves as a reminder of the balance between usefulness and safety in the field of chemistry!
Synonyms
4-Aminobiphenyl
92-67-1
4-Phenylaniline
4-Aminodiphenyl
4-BIPHENYLAMINE
[1,1'-Biphenyl]-4-amine
biphenyl-4-amine
Xenylamine
Biphenyl-4-ylamine
p-Biphenylamine
p-Phenylaniline
4-Biphenylylamine
p-Aminobiphenyl
p-Aminodiphenyl
p-Xenylamine
Biphenylamine
Paraaminodiphenyl
Xenylamin
4-Amino-1,1'-biphenyl
4-Aminodifenil
Aniline, p-phenyl-
4-Aminobifenyl
4-Bifenylamin
Xenylamin [Czech]
4-Bifenylamin [Czech]
4-Aminobifenyl [Czech]
NSC 7660
4-Aminodifenil [Spanish]
(1,1'-Biphenyl)-4-amine
CCRIS 26
HSDB 1325
(4-phenyl-phenyl)-amine
1,1'-biphenyl-4-amine
EINECS 202-177-1
Xenylamin (czech)
MFCD00007879
BRN 0386533
CHEBI:1784
DTXSID5020071
AI3-00124
UNII-16054949HJ
NSC-7660
4-Aminodifenil (spanish)
DTXCID9071
P-BIPHENYLAMINE [MI]
4-AMINODIPHENYL-D9
4-AMINOBIPHENYL [IARC]
4-BIPHENYLAMINE [HSDB]
16054949HJ
{[1,1'-Biphenyl]-4-amine}
NSC7660
4-12-00-03241 (Beilstein Handbook Reference)
biphenyl, 4-amino-
4-Bifenylamin (Czech)
4-Aminobifenyl (Czech)
EN300-17141
(1,1'-biphenyl)-4-ylamine
[1,1'-biphenyl]-4-ylamine
4-AMINOBIPHENYL (IARC)
((1,1'-Biphenyl)-4-amine)
116267-93-7
4-biphenylnitrenium ion
4-Aminobiphenyl min. 93%
pAminobiphenyl
pAminodiphenyl
pBiphenylamine
pPhenylaniline
pXenylamine
4aminobiphenyl
4biphenylamine
4phenylaniline
p-Aminobifenilo
4Aminobifenyl
4Aminodifenil
4Aminodiphenyl
4Bifenylamin
(1,1'-Biphenyl-4-yl)amine
4Biphenylylamine
4-Aminobifenilo
p-biphenyl amine
Aniline, pphenyl
p-Amino diphenyl
p-Phenyl aniline
para-aminobiphenyl
4-amino-biphenyl
4-phenyl aniline
4Amino1,1'biphenyl
P-DIPHENYLAMINE
1,1'Biphenyl)4amine
p-Aminobifenilo (Spanish)
WLN: ZR DR
4-Aminobifenilo (Spanish)
4-PHENYLBENZENEAMINE
4-ADP
SCHEMBL62469
MLS002303005
CHEMBL44201
4-Aminodiphenyl (ACGIH:OSHA)
MSK1201
BDBM626040
HMS1722B15
HMS3091M12
AAA09267
ALBB-025794
BCP25781
CS-B0270
QIA52772
4-Aminobiphenyl, analytical standard
Tox21_200376
STK315364
AKOS000114495
GS-3083
CAS-92-67-1
NCGC00091372-01
NCGC00091372-02
NCGC00091372-03
NCGC00257930-01
BP-11958
SMR000062444
DB-002657
4-Aminobiphenyl 10 microg/mL in Cyclohexane
NS00015359
[1,1'-biphenyl]-4-amine (ACD/Name 4.0)
[1,1'-biphenyl]-4-ylamine (ACD/Name 4.0)
A844308
AC-907/25014308
Q229922
F0096-0021
1,1'-Biphenyl-4-amine; 4-Biphenylylamine; 4-Phenylaniline
202-177-1
Solubility of 4-phenylaniline
4-phenylaniline, known for its unique structure, exhibits intriguing solubility characteristics that are essential for its application in various fields.
The solubility of 4-phenylaniline can be summarized with the following points:
In general, while 4-phenylaniline shows limited solubility in water, it can effectively dissolve in a range of organic solvents, making it valuable for specific industrial and research applications. As stated in common solubility concepts, “like dissolves like,” highlighting the importance of matching solvation properties for optimal dissolution.
Understanding the solubility of 4-phenylaniline is crucial for its utilization in synthesis and formulation processes, emphasizing the role of molecular interactions in achieving desired states in chemical formulations.