Interesting facts
Interesting Facts about 3-Methyl-4-Nitro-Phenol
3-Methyl-4-nitro-phenol, often referred to as metol, is a fascinating aromatic compound with a variety of applications and significance in both the chemical industry and scientific research. Here are some of the key points that highlight its importance:
- Analytical Chemistry: This compound is widely recognized for its role as a developer in photographic processes. It plays a pivotal role in developing black and white photographs by enhancing image contrast.
- Synthesis and Applications: 3-Methyl-4-nitro-phenol is not just a useful reagent; it is also a precursor for numerous dyes and pharmaceuticals, showcasing its versatility in organic synthesis.
- Biochemical Significance: Because of its nitro group, this compound exhibits interesting biochemical properties, making it a subject of study in toxicology and pharmacology. Understanding its metabolic pathways can help in assessing its impact on human health.
- Environmental Concerns: Like many nitro compounds, it poses certain environmental risks, particularly in the context of soil and water contamination. As scientists strive for greener chemistry, there is ongoing research to find less harmful alternatives.
- Chemical Reactions: 3-Methyl-4-nitro-phenol undergoes various chemical reactions such as nitration and methylation. These reactions are fundamental in organic chemistry for synthesizing more complex molecules.
- Laboratory Studies: Due to its distinct properties, this compound is frequently used in laboratory settings to study reaction kinetics and mechanisms, providing invaluable insights into chemical behavior.
In conclusion, 3-methyl-4-nitro-phenol is more than just a chemical compound; it is an integral part of numerous applications across various fields. Whether in photography, dye manufacture, or scientific research, its unique properties and reactions are essential for advancing our understanding of chemistry.
Synonyms
3-Methyl-4-nitrophenol
4-Nitro-m-cresol
4-Nitro-3-cresol
4-Nitro-3-methylphenol
Phenol, 3-methyl-4-nitro-
5-Methyl-4-nitrophenol
p-Nitro-m-methylphenol
EINECS 219-952-5
UNII-2CC94832EU
BRN 1868105
AI3-19030
NSC-69190
DTXSID2062535
CHEBI:38683
METHYL-4-NITROPHENOL, 3-
4-06-00-02075 (Beilstein Handbook Reference)
4Nitromcresol
4Nitro3cresol
mCresol, 4nitro
4Nitro3methylphenol
4Nitro5methylphenol
2Nitro5hydroxytoluene
5Hydroxy2nitrotoluene
Phenol, 3methyl4nitro
4Nitro1hydroxy3methylbenzene
DTXCID2037398
UN2446
inchi=1/c7h7no3/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4,9h,1h
piizynqecptveo-uhfffaoysa-n
2581-34-2
5-Hydroxy-2-nitrotoluene
2-Nitro-5-hydroxytoluene
4-Nitro-5-methylphenol
m-Cresol, 4-nitro-
P-NITRO-M-CRESOL
4-Nitro-1-hydroxy-3-methylbenzene
MFCD00007333
NSC 69190
2CC94832EU
p-?Nitro-?m-?cresol
3-methyl-4-nitro-phenol
4-NITRO-META-CRESOL
fenitrothion TP
NSC69190
3-Methyl-4-nitrophenol (4-Nitro-m-cresol)
WLN: WNR DQ B1
SCHEMBL214252
3-Methyl-4-nitrophenol, 98%
BBL011500
STL146612
AKOS000121313
AKOS040744799
AC-7840
CS-W023077
FM38675
AS-11958
DB-003082
3-Methyl-4-nitrophenol, analytical standard
N0351
NS00021951
EN300-18591
D70939
AE-562/43285825
Q27117943
Z85922875
F0001-0858
Solubility of 3-methyl-4-nitro-phenol
3-methyl-4-nitro-phenol, often represented by the chemical formula C7H7NO3, exhibits interesting solubility characteristics due to its molecular structure. This compound is known to be:
When discussing solubility, it's important to consider various factors:
In summary, while 3-methyl-4-nitro-phenol shows some solubility in water due to its functional groups, its true potential is unlocked in organic solvents. As with many phenols, the balance between hydrophilic and hydrophobic characteristics plays a crucial role in determining its solubility profile.