Interesting facts
Interesting Facts about 3,5-Dimethylphenol
3,5-Dimethylphenol, also known as p-cresol, is an intriguing compound that plays a significant role in various industrial applications. Here are some captivating facts:
- Structure and Isomerism: This compound is an example of a substituted phenol, where two methyl groups are positioned at the 3 and 5 locations of the phenol ring. This unique substitution pattern leads to interesting chemical behavior and reactivity.
- Natural Occurrence: 3,5-Dimethylphenol can be found in natural sources. It is often derived from the breakdown of certain organic materials, contributing to the natural aromatic profile of certain plants.
- Industrial Uses: It serves as a precursor in the synthesis of various chemicals, including pesticides and disinfectants. Its relevance in the production of phenolic resins makes it invaluable in the manufacturing of plastics.
- Biological Importance: This compound is known to exhibit antimicrobial properties, making it useful in preserving various materials and preventing microbial growth.
- Safety Considerations: As with many chemical compounds, handling 3,5-dimethylphenol requires caution. It can be harmful when ingested or inhaled, making safety protocols crucial in industrial settings.
In summary, 3,5-dimethylphenol is much more than just a chemical formula; it is a compound with diverse applications, natural occurrences, and significant implications for both industry and biology. As scientists continue to explore its properties, the potential advancements from its applications seem promising.
Synonyms
3,5-DIMETHYLPHENOL
108-68-9
3,5-Xylenol
Sym-m-xylenol
Phenol, 3,5-dimethyl-
1,3,5-Xylenol
3,5-Dmp
1-Hydroxy-3,5-dimethylbenzene
5-Hydroxy-m-xylene
Xylenol 200
3,5-Dimethyl phenol
NSC 9268
CCRIS 724
HSDB 5385
UNII-ONA760G0WA
Benzene, 1,3-dimethyl-5-hydroxy-
EINECS 203-606-5
DTXSID1025148
CHEBI:38572
3,5-Dimethyl-Phenol
AI3-01553
3,5-Xylen-1-ol
NSC-9268
MFCD00002307
ONA760G0WA
XYLENOL, 3,5-
DTXCID105148
1,3-Dimethyl-5-hydroxybenzene
1,5-Dimethyl-3-hydroxybenzene
1,5-Dimethyl-3-hyperoxybenzene
EC 203-606-5
XYLENOL 3,5-DIMETHYLPHENOL
3,5-DIMETHYLPHENOL [HSDB]
3,5-Dimethylphenol-2,4,6-d3
3,?5-?Dimethylphenol
XYLENOL 3,5-DIMETHYLPHENOL [MI]
3,5-DIMETHYLPHENOL [USP IMPURITY]
METACRESOL IMPURITY J [EP IMPURITY]
CAS-108-68-9
3,5-DIMETHYLPHENOL (USP IMPURITY)
METACRESOL IMPURITY J (EP IMPURITY)
symmXylenol
sym.-m-Xylenol
3.5-dimethylphenol
3, 5-dimethylphenol
1,3,5Xylenol
Phenol, 3,5dimethyl
M-5-XYLENOL
1Hydroxy3,5dimethylbenzene
SCHEMBL28714
3,5-Dimethylphenol, 98%
Benzene, 1,3dimethyl5hydroxy
WLN: QR C1 E1
3,5DMP
CHEMBL191740
3,5-Dimethylphenol, >=99%
NSC9268
Tox21_202181
Tox21_303372
STL194292
3,5-Dimethylphenol(1,3,5-Xylenol)
AKOS000119350
AC-7353
NCGC00091574-01
NCGC00091574-02
NCGC00257396-01
NCGC00259730-01
AS-13592
ERH
DB-030898
D0778
D1829
NS00008233
EN300-20196
3,5-Dimethylphenol 100 microg/mL in Methanol
D89931
3,5-Dimethylphenol, PESTANAL(R), analytical standard
Q26841188
F0001-0176
Z104477220
203-606-5
Solubility of 3,5-Dimethylphenol
3,5-dimethylphenol, also known as 2,6-dimethylphenol, exhibits notable solubility characteristics that are important for its applications in various chemical processes. Its solubility is influenced by the presence of the hydroxyl group (-OH) in its structure, which enhances its ability to interact with solvents.
Solubility Profile:
Overall, 3,5-dimethylphenol’s solubility aspects mean it can be utilized effectively in various industrial and chemical settings. As noted by scientists, “the balance of hydrophobic and hydrophilic interactions in molecules like this one plays a crucial role in their behavior in solution.”
In summary, the solubility of 3,5-dimethylphenol in different solvents underscores its versatility and utility in chemical synthesis and applications.