Interesting facts
Interesting Facts About 3-Aminophenol
3-Aminophenol, also known as meta-aminophenol, is an intriguing organic compound renowned for its diverse applications and fascinating properties. Here are some notable points about this unique compound:
- Key Role in Chemistry: 3-Aminophenol is a crucial building block in organic synthesis. Its amino group offers valuable reactivity, making it an essential reagent in producing dyes, pharmaceuticals, and agrochemicals.
- Photography and Color Chemistry: Historically, 3-aminophenol has been used in photographic development processes. Its ability to produce rich colors and enhance contrast has earned it a place in the realm of color chemistry.
- Biological Significance: Some studies suggest that 3-aminophenol can also have antioxidant properties. Research continues to explore its potential benefits in biomedical fields, particularly in developing therapeutics.
- Safety Precautions: While 3-aminophenol is valuable, it’s essential to handle it with care. Exposure can lead to skin irritation and respiratory issues; thus, proper laboratory safety protocols must be in place.
- Versatile Applications: This compound finds its utility in various industries, including the manufacture of hair dyes, pharmaceuticals for pain relief, and as a precursor for various chemical products.
In conclusion, 3-aminophenol exemplifies the intersection of chemistry and practical applications. Its ability to serve multiple roles in industry and research continues to pique the interest of chemists and students alike.
Synonyms
3-Aminophenol
M-AMINOPHENOL
Phenol, 3-amino-
3-amino-phenol
BASF ursol EG
m-Aminofenol
CI Oxidation Base 7
m-Aminofenol [Czech]
3-hydroxybenzenamine
NSC 1546
CCRIS 4145
HSDB 2586
UNII-L3WTS6QT82
EINECS 209-711-2
COVASTYLE MAP
DTXSID3024497
CHEBI:28924
COLOREX MAP
JAROCOL MAP
AI3-14871
RODOL EG
ORISTAR APH3
NSC-1546
PHENOL,3-AMINO
M-AMINOPHENOL [MI]
UN 2512 (Salt/Mix)
3-AMINOPHENOL [HSDB]
DTXCID704497
M-AMINOPHENOL [USP-RS]
EC 209-711-2
m-Aminofenol (Czech)
MESALAZINE IMPURITY B [EP IMPURITY]
M-AMINOPHENOL (USP-RS)
MESALAZINE IMPURITY B (EP IMPURITY)
mAminofenol
mAminophenol
mHydroxyaniline
3hydroxyaniline
Phenol, mamino
Phenol, 3amino
mHydroxyphenylamine
-Hydroxybenzenamine
mHydroxyaminobenzene
1Amino3hydroxybenzene
3Amino1hydroxybenzene
3-Hydroxyanilinel AC
PELAGAL EG
TETRAL EG
BASF URSOL BG
M-AMINOPHENOL [INCI]
cwlkgdavcfywjk-uhfffaoysa-n
inchi=1/c6h7no/c7-5-2-1-3-6(8)4-5/h1-4,8h,7h
un2512
591-27-5
3-Hydroxyaniline
m-Hydroxyaniline
1-Amino-3-hydroxybenzene
3-Amino-1-hydroxybenzene
m-Hydroxyaminobenzene
Fouramine EG
Futramine EG
Fourrine EG
Pelagol EG
Tertral EG
Furro EG
Renal EG
Ursol EG
Fourrine 65
Nako TEG
Phenol, m-amino-
Zoba EG
m-Hydroxyphenylamine
C.I. Oxidation Base 7
MFCD00007786
C.I. 76545
3-azaniumylphenolate
CI 76545
L3WTS6QT82
aniline, 3-hydroxy-
meta-aminophenol
m-amino-phenol
3-amino phenol
phenmedipham TP2
Mesalazine Imp. B (EP); m-Aminophenol; 3-Aminophenol; Mesalazine Impurity B
3-hydroxy-aniline
K5V
m-aminophenol (M6)
amino-3-hydroxybenzene
3-Aminophenol, 98%
WLN: ZR CQ
SCHEMBL35586
MLS002415740
BIDD:ER0564
BIDD:GT0645
CHEMBL269755
3-Aminophenol, puriss., 99%
MSK9312
NSC1546
HMS3039L12
STR01006
Tox21_200706
BDBM50428384
STK258727
AKOS000118984
m-Aminophenol [UN2512] [Poison]
FH70888
PS-9279
NCGC00091247-01
NCGC00091247-02
NCGC00258260-01
BP-13467
CAS-591-27-5
SMR001370906
DB-024153
A0383
NS00005675
EN300-19292
VU0606052-1
C05058
3-Aminophenol, PESTANAL(R), analytical standard
Q779427
F3228-0191
Z104473438
m-Aminophenol, United States Pharmacopeia (USP) Reference Standard
3-Aminophenol, Pharmaceutical Secondary Standard; Certified Reference Material
Solubility of 3-Aminophenol
3-Aminophenol, characterized by its chemical formula C6H7NO, displays interesting solubility properties that are worth noting:
As a result, the solubility of 3-aminophenol can be summarized as follows:
In conclusion, 3-aminophenol demonstrates a fascinating variety of solubility traits that are influenced by its chemical structure, making it an interesting compound in both academic and industrial contexts.