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Thymol

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Identification
Molecular formula
C10H14O
CAS number
89-83-8
IUPAC name
5-isopropyl-2-methyl-phenol
State
State

At room temperature, thymol is a solid, specifically a crystalline solid.

Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2170g/mol
Density
1.0300g/cm3
Appearence

Thymol is a white crystalline substance of a pleasant aromatic odor, reminiscent of thyme. The crystals are often large and transparent, and thymol is commonly used in its crystallized form.

Comment on solubility

Solubility of 5-isopropyl-2-methyl-phenol

The compound 5-isopropyl-2-methyl-phenol, commonly known as a type of substituted phenol, presents an intriguing profile when it comes to solubility. This organic compound is likely to exhibit the following solubility characteristics:

  • Polar Solvents: 5-isopropyl-2-methyl-phenol tends to be soluble in polar solvents due to the presence of the hydroxyl (-OH) group which engages in hydrogen bonding.
  • Non-Polar Solvents: While primarily polar, certain conditions may allow partial solubility in non-polar solvents, albeit to a lesser extent.
  • Water Solubility: The actual solubility in water can vary; the bulky isopropyl group may hinder complete solubility compared to simpler phenolic compounds.

In practical terms, you might find that:

  • The compound is more soluble in alcohols and other organic solvents.
  • Solubility in water may be limited, depending on the concentration and temperature.

To summarize, understanding the solubility of 5-isopropyl-2-methyl-phenol is vital for applications in drug formulation, environmental chemistry, and industrial processes. As with many organic compounds, structure plays a key role in influencing solubility characteristics.

Interesting facts

Interesting Facts about 5-Isopropyl-2-methyl-phenol

5-Isopropyl-2-methyl-phenol, often known as a powerful antimicrobial agent, plays a significant role in various industrial and pharmaceutical applications. Here are some engaging insights about this unique compound:

  • Antimicrobial Properties: This compound is widely recognized for its ability to inhibit the growth of bacteria and fungi. It is commonly utilized in products such as antiseptics and disinfectants.
  • Flavor and Fragrance: 5-Isopropyl-2-methyl-phenol is not just functional; it also has a distinctive aroma, making it useful in flavoring agents and fragrances, particularly in the food and cosmetic industries.
  • Chemical Versatility: This compound can serve as a precursor for the synthesis of other important chemical derivatives, showcasing its versatility in organic chemistry.
  • Environmental Impact: The use of this compound raises important discussions about sustainability and environmental safety, leading scientists to explore greener alternatives.
  • Research and Development: Ongoing studies are delving into the potential therapeutic applications of 5-isopropyl-2-methyl-phenol in treating various health conditions due to its biochemical properties.

Quote of the day: "Chemistry is the melody of science." - Anonymous This compounds' multifaceted applications truly embody this sentiment, as it harmonizes across different fields of study, enhancing our understanding and use of chemical compounds in everyday life.

In summary, 5-Isopropyl-2-methyl-phenol is not just a simple chemical entity; it represents the intersection of science, industry, and health, making it an intriguing topic of study for chemists and researchers alike.

Synonyms
CARVACROL
5-Isopropyl-2-methylphenol
499-75-2
Antioxine
2-p-Cymenol
5-Isopropyl-o-cresol
o-Thymol
Karvakrol
2-Hydroxy-p-cymene
p-Cymen-2-ol
2-Methyl-5-isopropylphenol
3-Isopropyl-6-methylphenol
p-Cymene, 2-hydroxy-
o-Cresol, 5-isopropyl-
2-Methyl-5-(Propan-2-Yl)Phenol
6-Methyl-3-isopropylphenol
1-Hydroxy-2-methyl-5-isopropylbenzene
FEMA No. 2245
Phenol, 5-isopropyl-2-methyl-
Cymene-2-ol, p-
Caswell No. 511
Phenol, 3-isopropyl-6-methyl-
1-Methyl-2-hydroxy-4-isopropylbenzene
DENTOL
NSC 6188
CCRIS 7450
HSDB 906
NSC-6188
EINECS 207-889-6
EPA Pesticide Chemical Code 022104
UNII-9B1J4V995Q
BRN 1860514
CHEBI:3440
AI3-03438
9B1J4V995Q
4-06-00-03331 (Beilstein Handbook Reference)
O-CRESOL, 5-ISOPROPYL
207-889-6
Isopropyl-o-cresol
Isothymol
Phenol, 2-methyl-5-(1-methylethyl)-
2-methyl-5-propan-2-ylphenol
2-Methyl-5-(1-methylethyl)phenol
5-Isopropyl-2-methyl-phenol
Oxycymol
MFCD00002236
CHEMBL281202
DTXSID6042074
2-methyl-5-propan-2-yl-phenol
2-Methyl-5-(1-methylethyl)-Phenol
Cymenol
2-Hydroxycymene
CYMOPHENOL
Hydroxy-p-cymene
p-Cymene-2-ol
Carvacrol, 98%
Carvacrol (Standard)
CARVACROL [FCC]
CARVACROL [MI]
CARVACROL [FHFI]
CARVACROL [HSDB]
CARVACROL [WHO-DD]
SCHEMBL24734
3-Isopropyl-6-methyl phenol
3-Isopropyl-6-methyl-Phenol
BIDD:ER0492
Carvacrol, analytical standard
GTPL2497
Carvacrol, natural, 99%, FG
DTXCID4022074
Methyl-5-(1-methylethyl)phenol
p-Mentha-1,3,5-trien-2-ol
WLN: QR B1 EY1&1
FEMA 2245
HY-N0711R
NSC6188
Carvacrol, >=98%, FCC, FG
HY-N0711
MSK40100
Tox21_301378
BDBM50240433
s3788
STL453136
AKOS000120828
AC-2688
CCG-266210
FS-4199
LMPR0102090017
MB00118
NCGC00256001-01
1ST40100
CAS-499-75-2
DA-49857
Isothymol (=2-Isopropyl-4-methyl phenol)
Carvacrol Cymenol 5-Isopropyl-2-methylphenol
CS-0009729
NS00004666
2-HYDROXY-4-ISOPROPYL-1-METHYLBENZENE
EN300-21426
C09840
F17722
Q225543
Carvacrol, primary pharmaceutical reference standard
BRD-K15541734-001-01-2
BRD-K15541734-001-02-0
BENZENE,2-HYDROXY,4-ISOPROPYL,1-METHYL CARVACROL
F8889-1978
Z104496566
BENZENE,2-HYDROXY,4-ISOPROPYL,1-METHYL CARVACROL
InChI=1/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H
S5V