Interesting facts
Interesting Facts about 2-Amino-4-phenyl-phenol
2-Amino-4-phenyl-phenol, often abbreviated as APAP, is a fascinating compound with significant applications in various fields. Here are some intriguing aspects of this chemical:
- Structure and Isomerism: The molecular structure of 2-amino-4-phenyl-phenol features an amino group attached to a phenolic compound. This structure allows the compound to exhibit isomerism, leading to different physical and chemical properties in related compounds.
- Corrosion Inhibition: One notable application of APAP is in the field of corrosion inhibition. It has been studied for its ability to protect metals from oxidization, providing a cost-effective means to prolong the life of materials and structures.
- Biomedical Applications: Research indicates that 2-amino-4-phenyl-phenol may possess biological activity, including antioxidant properties. Such characteristics make it a potential candidate for further investigation in pharmaceutical development.
- Colorimetric Analysis: This compound can also be utilized in analytical chemistry, particularly in colorimetric assays for specific analytes, thereby contributing to the accuracy and efficiency of various diagnostics.
- Environmental Considerations: As with many phenolic compounds, the use of 2-amino-4-phenyl-phenol in industrial applications raises concerns regarding its environmental impact. Effective management and disposal strategies are crucial to mitigate any potential risks to ecosystems.
In summary, 2-amino-4-phenyl-phenol is a compound with a wide range of applications and implications. Its multi-faceted nature makes it a subject of ongoing research and exploration within the scientific community.
Synonyms
2-Amino-4-phenylphenol
1134-36-7
3-Amino-4-hydroxybiphenyl
3-Aminobiphenyl-4-ol
[1,1'-Biphenyl]-4-ol, 3-amino-
2-Hydroxy-5-phenylaniline
4-Biphenylol, 3-amino-
Phenol, 2-amino-4-phenyl-
(1,1'-Biphenyl)-4-ol, 3-amino-
4-phenyl-2-aminophenol
NSC 7950
EINECS 214-484-8
NSC-7950
3-AMINO-4-BIPHENYLOL
3D49P06660
DTXSID8061553
AMINO-(1,1'-BIPHENYL)-4-OL, 3-
DTXCID6033326
3-Amino-[1,1'-biphenyl]-4-ol
3-amino-1,1'-biphenyl-4-ol
MLS000084764
MLS000737887
SMR000019110
2-amino-4-phenyl-phenol
NSC7950
UNII-3D49P06660
MFCD00059187
[1, 3-amino-
ChemDiv3_000220
2-azanyl-4-phenyl-phenol
2-hydroxy-5-phenyl aniline
Oprea1_652540
cid_14562
SCHEMBL305617
CHEMBL574583
BDBM37561
CHEBI:105700
HMS1473J22
HMS2363K13
KUC106663N
ALBB-024303
KSC-22-7
BBL008080
STK513465
3-Amino[1,1'-biphenyl]-4-ol #
AKOS000111159
CCG-103916
PS-8495
IDI1_019538
NCGC00045122-03
BP-30020
DB-022223
A0397
CS-0156457
MLS000084764-02
NS00023685
EN300-88962
2-Amino-4-phenylphenol, technical grade, 90%
A11905
3-Amino-4-hydroxybiphenyl;2-Amino-4-phenylphenol
SR-01000394316
SR-01000394316-1
BRD-K47707616-001-01-4
Q27183457
InChI=1/C12H11NO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h1-8,14H,13H
Solubility of 2-amino-4-phenyl-phenol
2-amino-4-phenyl-phenol, a compound characterized by its amino and phenolic groups, exhibits intriguing solubility properties. In general, its solubility is influenced by the following factors:
In terms of practical applications, **"the solubility of 2-amino-4-phenyl-phenol in water is relatively low"** compared to more soluble compounds, yet it can still readily dissolve in organic solvents, making it versatile for various chemical reactions and processes.
In summary, understanding the solubility of 2-amino-4-phenyl-phenol is essential for its effective application in research and industry. Its characteristics highlight the intricate interplay between molecular structure and solubility behavior.