Interesting facts
Interesting Facts about 2-Methoxy-4-methyl-phenol
2-Methoxy-4-methyl-phenol, often known as Thymol, is a fascinating compound that garners interest in both the scientific and commercial realms. Here are some engaging insights:
- Natural Antiseptic: Thymol is derived from thyme oil, and it is well-known for its antimicrobial properties. It has been shown to effectively combat various strains of bacteria, making it a valuable component in hand sanitizers and disinfectants.
- Flavor and Aroma: The compound possesses a unique flavor and aroma, contributing to its use in food products as a flavoring agent. Its spicy, warm notes are highly appreciated in culinary applications.
- Medicinal Use: Traditional medicine has utilized Thymol for centuries. It is reputed to support respiratory health, alleviating symptoms associated with cough and bronchitis, showcasing its potential therapeutic benefits.
- Insect Repellent: Thymol's strong scent acts as a natural repellent against certain insects, proving beneficial in both agriculture and home use. It is less harmful compared to synthetic alternatives.
- Research Interest: Current studies are exploring Thymol's potential role in combating antibiotic resistance, which is a growing concern in modern medicine. Its ability to disrupt bacterial cell membranes could lead to innovative treatments.
In summary, 2-Methoxy-4-methyl-phenol is not only important in various industries but also has significant implications for health, wellness, and environmental applications. As scientists, understanding the properties and potential of such compounds is essential for developing new, sustainable solutions.
Synonyms
2-METHOXY-4-METHYLPHENOL
93-51-6
Creosol
4-Methylguaiacol
Phenol, 2-methoxy-4-methyl-
2-Methoxy-p-cresol
4-Methyl guaiacol
p-Methylguaiacol
p-Creosol
Homoguaiacol
2-Methoxy-4-cresol
p-Cresol, 2-methoxy-
4-Hydroxy-3-methoxytoluene
4-Methyl-2-methoxyphenol
Kreosol
Rohkcrsol
2-methoxy-4-methyl-phenol
3-Methoxy-4-hydroxytoluene
Cresolum drudum
4-Hydroxy-3-methoxy-1-methylbenzene
Homocatechol monomethyl ether
Kreosol [German]
Valspice
1-Hydroxy-2-methoxy-4-methylbenzene
FEMA No. 2671
NSC 4969
MFCD00002378
UNII-W9GW1KZG6N
W9GW1KZG6N
2-Hydroxy-5-methylanisole
2-methoxy-4-methyl phenol
EINECS 202-252-9
Phenol, 4-methyl-2-methoxy
BRN 1862340
DTXSID6047105
AI3-15891
NSC-4969
CREOSOL [MI]
DTXCID4027105
CHEBI:89886
NSC4969
4-06-00-05878 (Beilstein Handbook Reference)
2-METHOXY-4-METHYLPHENOL [FHFI]
2-?Methoxy-?4-?methylphenol
2-2-Methoxy-4-methylphenol
P-Methylguaicol
4-Methylguiacol
Creosol (Standard)
Homocatechol methyl ester
2-Methoxy-4-methylphenol (Methyl guaiacol)
3-Methoxy-4-methyl-Phenol
SCHEMBL92236
2-METHOXY-P- CRESOL
CHEMBL3182715
2-Methoxy-4-methylphenol, 9CI
FEMA 2671
BCP19090
HY-W040971R
2-Methoxy-4-methylphenol (creosol)
Tox21_302681
2-Methoxy-4-methylphenol, >=98%
AKOS000120520
CS-W021711
FM36438
HY-W040971
CAS-93-51-6
NCGC00256731-01
2-Methoxy-4-methylphenol, >=98%, FG
AS-15967
SY036778
2-Methoxy-4-methylphenol (4-methylguaiacol)
4-Methyl-2-methoxyphenol (4-methylguaiacol)
M0114
NS00012823
2-Methoxy-4-methylphenol, analytical standard
EN300-18155
2-Methoxy-4-methylphenol, natural, 97%, FG
D70655
Q403037
2-Methoxy-p-cresol;Creosol;2-Methoxy-4-methylphenol
Z57234300
F0001-2237
Solubility of 2-methoxy-4-methyl-phenol
2-methoxy-4-methyl-phenol, also known as p-cresol methyl ether, exhibits interesting solubility properties that are important for its practical applications. This compound is characterized by its moderately polar structure, which influences its interaction with various solvents.
Key Points on Solubility:
Overall, the solubility characteristics of 2-methoxy-4-methyl-phenol play a crucial role in its reactivity and efficacy as a chemical compound. The balance of its polar and non-polar attributes makes it versatile yet somewhat challenging in aqueous environments.