Interesting facts
Exploring 2,3,6-Trimethylphenol
2,3,6-trimethylphenol, also known as pseudo-cresol, is an intriguing chemical compound that belongs to the class of phenols. Here are some fascinating facts that showcase the significance of this compound in the field of chemistry:
- Structure and Isomerism: The structure of 2,3,6-trimethylphenol is notable because it features three methyl groups attached to a benzene ring. This arrangement grants the compound unique properties and makes it a subject of interest for studies in isomerism.
- Applications in Industry: This compound plays a crucial role in the synthesis of a variety of chemical products, particularly in the manufacturing of fragrances and flavoring agents. Its versatility allows it to be incorporated into numerous formulations.
- Antioxidant Properties: 2,3,6-trimethylphenol exhibits antioxidant characteristics, making it valuable in preserving food substances and preventing oxidative deterioration in several industrial applications.
- Health and Safety Considerations: As with many phenolic compounds, safety precautions are essential. It is crucial to handle this compound with care, as it can be irritating to the skin and eyes. Proper laboratory protocols should always be followed.
- Natural Occurrence: Interestingly, 2,3,6-trimethylphenol occurs naturally in certain plant sources, particularly in essential oils. This natural occurrence adds to its importance in both synthetic chemistry and natural product chemistry.
In summary, 2,3,6-trimethylphenol is not just a chemical compound but a fascinating subject of study that bridges both industrial applications and natural chemistry. As scientists continue to explore its properties and uses, this compound remains a key player in various fields.
Synonyms
2,3,6-TRIMETHYLPHENOL
2416-94-6
3-Hydroxypseudocumene
Phenol, 2,3,6-trimethyl-
1-Hydroxy-2,3,6-trimethylbenzene
HSDB 5876
UNII-05WKL2L5LJ
EINECS 219-330-3
05WKL2L5LJ
NSC 91509
DTXSID6022187
NSC-91509
DTXCID602187
FEMA NO. 3963
EC 219-330-3
2,3,6-TRIMETHYLPHENOL [FHFI]
2,3,6-TRIMETHYLPHENOL [HSDB]
3Hydroxypseudocumene
Phenol, 2,3,6trimethyl
1Hydroxy2,3,6trimethylbenzene
219-330-3
inchi=1/c9h12o/c1-6-4-5-7(2)9(10)8(6)3/h4-5,10h,1-3h
qqomqlyqaxghsu-uhfffaoysa-n
un2430
2,3,6-trimethyl-phenol
MFCD00002229
fema 3963
CAS-2416-94-6
2,3,6-TRIMETHYL PHENOL
NSC91509
2,5,6-trimethylphenol
SCHEMBL23915
CHEMBL3182738
2,3,6-Trimethylphenol, 95%
CHEBI:169180
Tox21_202274
Tox21_300059
1-Hydroxy-2,3, 6-trimethylbenzene
STL280176
AKOS000120327
CCG-302510
FT54823
NCGC00247892-01
NCGC00247892-02
NCGC00253981-01
NCGC00259823-01
AC-10656
LS-13646
CS-0186482
NS00006095
T0877
EN300-20609
Q27236151
Z104479158
25511-57-3
Solubility of 2,3,6-trimethylphenol
2,3,6-trimethylphenol, a compound with the formula C10H14O, exhibits intriguing solubility characteristics that are influenced by its molecular structure and functional groups. Understanding its solubility helps chemists in applications where this compound is utilized.
Key Aspects of Solubility
When exploring the solubility of 2,3,6-trimethylphenol, consider the following:
As a general rule, the greater the number of non-polar hydrocarbon chains, the lower the solubility in water. Therefore, while 2,3,6-trimethylphenol can dissolve to some extent in water, its solubility is significantly enhanced in organic solutions. This understanding is crucial for applications in industrial and laboratory settings.
To sum up, while 2,3,6-trimethylphenol displays some solubility in water due to the hydroxyl functional group, it is predominantly more soluble in non-polar or moderately polar solvents, showcasing the balance between hydrophilic and hydrophobic attributes.