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Isopulegol

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Identification
Molecular formula
C10H18O
CAS number
89-79-2
IUPAC name
4-isopropenyl-1-methyl-cyclohexanol
State
State

At room temperature, isopulegol is typically a solid.

Melting point (Celsius)
-35.50
Melting point (Kelvin)
237.70
Boiling point (Celsius)
212.50
Boiling point (Kelvin)
485.60
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
0.9133g/cm3
Appearence

Isopulegol appears as a colorless or white crystalline solid. It has a distinctive minty aroma and is often a constituent of the essential oils of various plants.

Comment on solubility

Solubility of 4-isopropenyl-1-methyl-cyclohexanol

The solubility of 4-isopropenyl-1-methyl-cyclohexanol can be quite fascinating, as it demonstrates the properties associated with organic compounds. This compound, being a secondary alcohol, showcases a few key characteristics in terms of solubility:

  • Polar vs. Non-Polar: The presence of the hydroxyl group (-OH) in its structure allows for hydrogen bonding, which generally enhances solubility in polar solvents, such as water.
  • Hydrophobic Components: The isopropenyl and methyl groups introduce hydrophobic characteristics, meaning that less polar solvents, like organic solvents (e.g., ethanol or acetone), will likely dissolve it better.
  • Temperature Influence: Solubility can also be affected by temperature; typically, increasing temperature enhances the solubility of many organic compounds.

In summary, while 4-isopropenyl-1-methyl-cyclohexanol may exhibit limited solubility in water due to its hydrophobic nature, it is expected to have good solubility in organic solvents. As with many chemical compounds, it illustrates the balance between polar and non-polar interactions. Therefore, for practical applications and experimental design, consideration of the solvent choice is crucial.

Interesting facts

Interesting Facts about 4-isopropenyl-1-methyl-cyclohexanol

4-isopropenyl-1-methyl-cyclohexanol is a fascinating compound known for its unique structure and properties. Here are some intriguing aspects of this compound:

  • Structural Complexity: The compound features a cyclohexanol ring, which introduces an element of cyclic stability, coupled with an isopropenyl group that can participate in various chemical reactions.
  • Chemical Reactivity: The double bond present in the isopropenyl group makes this compound susceptible to electrophilic addition reactions, which can lead to the formation of a plethora of derivatives.
  • Natural Occurrence: Compounds similar to 4-isopropenyl-1-methyl-cyclohexanol often occur in nature, particularly in essential oils. They can contribute to the aromas and flavors of several plants, making them relevant in the fields of food and fragrance chemistry.
  • Applications: This compound has potential applications in the pharmaceutical and fragrance industries due to its unique scent and biological properties. It may serve as a precursor to more complex molecules or as an active ingredient in various formulations.
  • Synthesis Routes: Chemists can utilize various synthetic routes to obtain 4-isopropenyl-1-methyl-cyclohexanol, which often involve starting materials like terpenes or other cyclic alcohols. This versatility can make it an interesting subject for synthetic organic chemistry studies.

In summary, 4-isopropenyl-1-methyl-cyclohexanol serves as an excellent example of how structural diversity in organic compounds can lead to a wide array of uses and chemical behaviors, making it a worthwhile topic for exploration in both academia and industry.

Synonyms
BETA-TERPINEOL
138-87-4
cis-beta-Terpineol
trans-beta-Terpineol
p-Menth-8-en-1-ol
Cyclohexanol, 1-methyl-4-(1-methylethenyl)-
trans-|A-Terpineol
1-Methyl-4-(1-methylethenyl)cyclohexanol
cis-.beta.-Terpineol
1-Methyl-4-(1-methylvinyl)cyclohexan-1-ol
trans-.beta.-terpineol
1-Methyl-4-isopropenylcyclohexan-1-ol
4-Isopropenyl-1-methyl-1-cyclohexanol
1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol
7299-40-3
4-Isopropenyl-1-methylcyclohexanol
cis-|A-Terpineol
(E)-beta-Terpineol
7299-41-4
Cyclohexanol, 1-methyl-4-(1-methylethenyl)-, trans-
1-methyl-4-prop-1-en-2-ylcyclohexan-1-ol
Terpineol, cis-.beta.-
Cyclohexanol, 1-methyl-4-(1-methylethenyl)-, cis-
S00R85C5ER
DTXSID7041209
55258Z4SCW
p-Menth-8-en-1-ol, stereoisomer
Terpinol, beta-
t-Menth-1-en-8-ol
b-terpineol
FEMA No. 3564
beta-Terpineol, cis-
beta-Terpineol, trans-
EINECS 205-342-6
UNII-XS86XKC2VT
BRN 2205072
UNII-S00R85C5ER
beta-Terpinol
UNII-55258Z4SCW
beta -terpineol
AI3-00731
4-isopropenyl-1-methyl-cyclohexanol
cis-I(2)-Terpineol
trans-I(2)-Terpineol
(E)-.beta.-terpineol
(Z)-.beta.-Terpineol
XS86XKC2VT
cis-p-Menth-8-en-1-ol
trans-p-Menth-8-en-1-ol
P-menth-8-en-1-ol, cis
4-06-00-00254 (Beilstein Handbook Reference)
SCHEMBL1245775
.BETA.-TERPINEOL, CIS-
CHEMBL3184678
DTXCID5021209
SCHEMBL13895789
SCHEMBL14278527
SCHEMBL22882350
FEMA 3564
.BETA.-TERPINEOL, TRANS-
CHEBI:132899
DTXSID201317014
DTXSID301316364
Tox21_302378
MFCD00037724
AKOS006282035
HY-119963A
HY-119963B
4-Isopropenyl-1-methylcyclohexanol, cis
NCGC00255487-01
CAS-138-87-4
DA-69594
DA-78581
1-Methyl-4-(1-Methylethenyl)-cyclohexanol
4-Isopropenyl-1-methylcyclohexanol, trans-
DB-243107
CS-0089116
CS-0089118
NS00012934
C17517
1-Methyl-4-(1-methylethenyl)-trans-Cyclohexanol
1beta-Methyl-4alpha-(1-methylethenyl)cyclohexanol
TERPIN MONOHYDRATE IMPURITY B [EP IMPURITY]
Q27261256
Q27288363
Q67880219
Rel-(1r,4r)-1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol
(1S,4S)-1-METHYL-4-(PROP-1-EN-2-YL)CYCLOHEXAN-1-OL
844-907-7