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Thymol

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Identification
Molecular formula
C10H14O
CAS number
89-83-8
IUPAC name
2-isopropylphenol
State
State

At room temperature, thymol is typically a solid. It is known for its stability under normal conditions, making it convenient for various applications, including its use as a preservative and antiseptic.

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
150.2180g/mol
Density
0.9601g/cm3
Appearence

Thymol appears as a white crystalline solid with a characteristic aromatic odor. It is known for its pleasant and distinctly pungent scent which is reminiscent of thyme, from which it is often derived.

Comment on solubility

Solubility of 2-isopropylphenol

2-isopropylphenol, also known as p-iso-propylphenol, exhibits unique solubility characteristics that are essential for its various applications in chemical processes. Here are some key points regarding its solubility:

  • Solvent Compatibility: 2-isopropylphenol is primarily soluble in organic solvents such as ethanol, methanol, and chloroform.
  • Water Solubility: This compound exhibits limited solubility in water, primarily due to its hydrophobic isopropyl group, which impedes interaction with polar solvents.
  • Temperature Influence: Solubility can vary with temperature; generally, increased temperature enhances its solubility in organic solvents.
  • pH Effect: The solubility can also be affected by the pH of the solution, particularly in cases involving aqueous environments.

In practical applications, understanding the solubility of 2-isopropylphenol is crucial as it influences reaction kinetics and product formulation. As one might say, "A compound's worth is often reflected in its ability to dissolve and interact." Thus, the solubility profile of 2-isopropylphenol plays a pivotal role in its utility in various chemical and industrial processes.

Interesting facts

Interesting Facts about 2-Isopropylphenol

2-Isopropylphenol, also known as p-cumenol, is a fascinating compound with a myriad of applications and chemical behaviors that set it apart in the realm of organic chemistry.

Unique Properties and Uses

  • Antibacterial Activity: 2-Isopropylphenol exhibits noteworthy antibacterial properties, making it valuable in various healthcare and pharmaceutical applications.
  • Flavor and Fragrance: This compound is often used in the production of flavors and fragrances, adding a distinctive profile to products. Its pleasant aroma is utilized in the cosmetic industry as well.
  • Industrial Applications: In addition to its use in consumer products, it serves as a reagent in organic synthesis and can act as a stabilizer in plastics and resins.

Chemical Behavior

When examining the chemical structure of 2-isopropylphenol, one can appreciate the significance of its isopropyl group, which influences its reactivity and interactions. This group enhances the compound's hydrophobic characteristics, allowing it to integrate well with lipid membranes.

Environmental Impact

Interestingly, the compound's biodegradability has attracted attention within environmental science. Its breakdown products are less harmful, which positions it as a more environmentally friendly alternative compared to other phenolic compounds.

Fun Fact

In the world of research, chemists often marvel at the symmetry and reactivity of organic compounds. With 2-isopropylphenol, one can easily highlight the significance of substituents on aromatic rings, which can drastically change the properties and behaviors of compounds. It's a classic example that makes you ponder the wonders of organic chemistry!

In summary, 2-isopropylphenol is more than a simple chemical compound; it's a versatile ingredient in modern science with beneficial properties that are valuable across industries.

Synonyms
2-Isopropylphenol
88-69-7
O-ISOPROPYLPHENOL
o-Hydroxycumene
ISOPROPYLPHENOL
2-(1-Methylethyl)phenol
o-Cumenol
Phenol, o-isopropyl-
1-Hydroxy-2-isopropylbenzene
2-propan-2-ylphenol
Phenol, 2-(1-methylethyl)-
2-(propan-2-yl)phenol
Prodox 131
ISOPROPYLPHENOL, ORTHO
1-Hydroxy-3-isopropylbenzene
Cumenol, o-
Isopropylphenol, o-
ortho-isopropylphenol
2-Hydroxycumene
FEMA No. 3461
2-Isopropyl phenol
2-Isopropyl-Phenol
NSC 5103
25168-06-3
isopropyl-phenol
o-isopropyl-phenol
EINECS 201-852-8
UNII-B2899Z0Q2U
BRN 1363322
DTXSID2044391
CHEBI:38506
AI3-18550
B2899Z0Q2U
NSC-5103
MFCD00002224
2-(1-Methylethyl)-Phenol
ISOPROPYLPHENOL, 2-
CHEMBL30018
DTXCID0024391
2-(1-Methylethyl)phenol, 9CI
FEMA 3461
2-ISOPROPYLPHENOL [FHFI]
4-06-00-03210 (Beilstein Handbook Reference)
PROPOFOL IMPURITY C [EP IMPURITY]
METACRESOL IMPURITY H [EP IMPURITY]
cumenol
PROPOFOL IMPURITY C (EP IMPURITY)
METACRESOL IMPURITY H (EP IMPURITY)
oHydroxycumene
oCumenol
oIsopropylphenol
isopropyl phenol
oIsopropyl phenol
2-(1-Methylethyl)phenol; Propofol Imp. C (EP); Propofol Impurity C
2isopropyl phenol
Cumenol, o
Isopropylphenol, o
Phenol, oisopropyl
0-isopropyl phenol
2-iso-propylphenol
Phenol, isopropyl-
ortho-isopropyl phenol
phenol, 2-isopropyl-
2(1Methylethyl)phenol
1Hydroxy2isopropylbenzene
Phenol, 2(1methylethyl)
2-Isopropylphenol, 98%
UNII-7UD6MUG48S
7UD6MUG48S
SCHEMBL43297
SCHEMBL8988162
NSC5103
3f36
2-Isopropylphenol, >=98%, FG
EINECS 246-699-8
Tox21_302062
BDBM50409533
STL453618
AKOS000120752
FI35506
CAS-88-69-7
NCGC00255940-01
BP-10159
PD055451
I0173
NS00021381
EN300-20953
G77227
Q27117882
F0001-2189
Z104485440
201-852-8
IP0