Interesting facts
Interesting Facts About 4-phenylazoaniline
4-phenylazoaniline, also known as aniline yellow, is a fascinating compound in the realm of organic chemistry, particularly due to its vibrant color and functional properties. Here are some key facts that highlight the significance of this compound:
- Color Properties: The presence of the azo group (–N=N–) contributes to its intense yellow color, making it a popular dye in the textile and food industries.
- Applications: This compound is widely utilized not only as a dye but also as an intermediate in the synthesis of pigments and other organic compounds. Its ability to impart color makes it valuable in various applications.
- Historical Context: 4-phenylazoaniline has historical significance as one of the early synthetic dyes, arising during the late 19th century when synthetic organic chemistry began to flourish.
- Reactivity: The compound exhibits reactivity typical of azo compounds, which undergo reactions such as reduction and diazotization, making it a versatile building block in organic synthesis.
- Environmental Considerations: While it has notable applications, it is critical to consider the environmental impact of azo dyes, as some can break down into harmful amines under certain conditions.
In summary, 4-phenylazoaniline is not just another chemical compound; its vibrant hue and utility in the dye industry render it an interesting subject of study. The impact it has had on both chemistry and industry illustrates the fascinating intersection of science and practical application. As a student or scientist, exploring its properties and potential offers a deeper understanding of organic compounds and their implications in everyday life.
Synonyms
4-Aminoazobenzene
60-09-3
p-Aminoazobenzene
Benzenamine, 4-(phenylazo)-
ANILINE YELLOW
4-(Phenylazo)aniline
Aminoazobenzene
4-Phenylazoaniline
Cellitazol R
Solvent Yellow 1
4-(Phenylazo)benzenamine
Organol Yellow
4-(phenyldiazenyl)aniline
C.I. Solvent Yellow 1
Induline R
Sudan Yellow R
Sudan Yellow RA
Stearix Brown 4R
Organol Yellow 2A
p-Aminodiphenylimide
Somalia Yellow 2G
p-Aminoazobenzol
4-Amino-1,1'-azobenzene
4-Aminoazobenzol
C.I. Solvent Blue 7
p-(Phenylazo)aniline
Ceres Yellow R
Fat Yellow AAB
Azobenzene, 4-amino-
4-Benzeneazoaniline
p-(Phenolazo)aniline
25548-34-9
Aniline, p-(phenylazo)-
Usaf ek-1375
Paraphenolazo aniline
Zlut anilinova
(E)-4-(phenyldiazenyl)aniline
Aminoazobenzene (indicator)
p-Phenylazophenylamine
Zlut rozpoustedlova 1
C.I. 11000
4-phenyldiazenylaniline
4-Phenylazo-phenylamine
p-Amimoazobenzene
Zlut anilinova [Czech]
Zlut rozpoustedlova 1 [Czech]
4-[(E)-Phenyldiazenyl]aniline
p-(Phenylazo)phenylamine
p-Phenylazoaniline
4-[(E)-2-phenyldiazen-1-yl]aniline
p-Aminodiphenyldiimide
4-Phenylazophenylamine
DTXSID6024460
p-AAZB
4-(2-phenyldiazen-1-yl)aniline
CHEBI:233869
4-[phenyldiazenyl]aniline
Benzenamine, 4-(2-phenyldiazenyl)-
MFCD00007854
4-AAB
DTXCID004460
AAB
57X2AH42T1
NSC-2032
Benzenamine, 4-[(1E)-phenylazo]-
para-Aminoazobenzene
4-[(1E)-2-phenyldiazen-1-yl]aniline
NCGC00164077-02
p-Phenylazonaniline
4-Aminoazobenzene 100 microg/mL in Acetonitrile
8004-98-6
4-[(E)-2-phenyldiazenyl]aniline
ZLUT ANILINOVA (CZECH)
CI Solvent Yellow 1
Aniline Yellow (VAN)
Solvent Yellow
ZLUT ROZPOUSTEDLOVA 1 (CZECH)
CCRIS 24
HSDB 2137
NSC 2032
EINECS 200-453-6
CI 11000
UNII-57X2AH42T1
AI3-00793
p-Aminoazaobenzene
4-Amino-azobenzene
Benzenamine, 4-(phenylazo)-, (E)-
4-Aminoazobenzene; Azo
WLN: ZR DNUNR
4-Aminoazobenzene, 98%
Epitope ID:116049
4-[phenyldiazenyl] aniline
EC 200-453-6
4-[(E)-phenylazo]aniline
AMINOAZOBENZENE, 4-
4-(Phenyldiazenyl)aniline #
MLS000419131
ANILINE YELLOW [HSDB]
CHEMBL83761
SCHEMBL208182
P-AMINOAZOBENZENE [MI]
CHEMBL1429559
DTXSID5093684
DTXSID40859039
MSK1222
NSC2032
Benzenamine,4-(phenylazo)-(E)-
HMS2702P12
AAA06009
STR02191
EINECS 232-333-4
Tox21_400019
BBL010329
STK801547
4-Aminoazobenzene, analytical standard
AKOS000319539
AKOS028110059
4-[(1E)-2-Phenyldiazenyl]benzenamine
4-(2-PHENYLDIAZENYL)BENZENAMINE
CAS-60-09-3
NCGC00164077-01
NCGC00164077-03
NCI60_001708
SMR000319771
SY050979
VS-02450
NS00008368
P0141
EN300-18330
C19187
D91909
AC-907/25014309
AE-848/00954057
Q546957
Z57902184
F0020-1827
22-16-2
Solubility of 4-phenylazoaniline (C12H11N3)
4-phenylazoaniline exhibits interesting solubility characteristics that stem from its chemical structure. The compound's solubility can be influenced by several factors, including:
In summary, while 4-phenylazoaniline can dissolve in polar solvents due to the presence of functional groups capable of hydrogen bonding, it is more effectively soluble in non-polar or slightly polar organic solvents. This dual solubility characteristic makes it versatile for different chemical processes.
“A careful examination of solution strategies must consider both the polarity of the compound and the solvent interaction,” as highlighted by solubility experts.