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Menthol

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Identification
Molecular formula
C10H18O
CAS number
78-70-6
IUPAC name
2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol
State
State

At room temperature, the compound can be either a liquid or a crystalline solid depending on isomeric form and purity. It often appears as a slightly viscous liquid.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
126.00
Boiling point (Kelvin)
399.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
0.8970g/cm3
Appearence

2,2,6-Trimethyl-6-vinyl-tetrahydropyran-3-ol is a colorless, clear liquid or crystalline solid with a peppermint-like odor. It is a versatile compound known for its minty scent and is commonly used in the flavor and fragrance industries.

Comment on solubility

Solubility of 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol

The solubility of 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol can be assessed based on its chemical structure, which indicates specific interactions with solvents. This compound is characterized by a tetrahydropyran ring with hydroxyl (–OH) functional groups that significantly influence its solubility properties.

Key Factors Affecting Solubility:

  • Polarity: The presence of the hydroxyl group contributes to the polarity of the molecule, facilitating interactions with polar solvents such as water.
  • Hydrophobic Effects: The bulky hydrophobic groups (e.g., methyl and vinyl) may decrease its overall solubility in non-polar solvents.
  • Temperature: As with many organic compounds, increased temperature typically enhances solubility in various solvents.

In summary, while the hydroxyl group suggests a degree of solubility in polar solvents, the presence of larger hydrophobic regions may limit overall solubility in non-polar solvents. Given these factors, it is often necessary to conduct experimental evaluations to determine the specific solubility profile of 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol in various solvents. As we explore its applications, understanding its solubility will be crucial!

Interesting facts

Interesting Facts about 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol

2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol is a fascinating compound that showcases the intricate beauty of organic chemistry. Here are some key insights into this unique chemical:

  • Structural Diversity: The compound features a distinctive tetrahydropyran ring structure, which is a six-membered ring containing one oxygen atom. This topology plays a crucial role in the compound's reactivity and properties.
  • Functional Groups: The presence of both vinyl and alcohol functional groups imbues the molecule with interesting reactivity. The vinyl group can participate in addition reactions, while the hydroxyl group can engage in hydrogen bonding, influencing solubility and interactions with biological systems.
  • Potential Applications: Given its unique structure, this compound holds promise in applications such as:
    • As a monomer in the synthesis of polymers, where its vinyl group can be utilized for polymerization reactions.
    • In the fragrance industry, as various cyclic alcohols are known to impart distinctive scents.
  • Synthetic Pathways: Creating this compound involves intricate synthetic pathways, often requiring multiple steps of functionalization and careful control of reaction conditions to maintain yield and purity.
  • Biological Significance: Compounds similar to 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol have been studied for their potential biological activities, including antimicrobial properties, making them useful in pharmaceutical research.

In conclusion, the study of 2,2,6-trimethyl-6-vinyl-tetrahydropyran-3-ol provides insights into the complex interactions of structure and function within organic compounds. As scientists explore its potential applications, it serves as a substantial example of how nuanced modifications in chemical structures can lead to a variety of outcomes in science and industry.

Synonyms
14049-11-7
2H-Pyran-3-ol, 6-ethenyltetrahydro-2,2,6-trimethyl-
Linalool Oxide Pyranoid
2H-Pyran-3-ol, tetrahydro-2,2,6-trimethyl-6-vinyl-
EINECS 237-889-1
Tetrahydro-2,2,6-trimethyl-6-vinyl-2H-pyran-3-ol
CJQ633A12A
DTXSID00864462
2H-Pyran-3-ol, 6-ethenyl-tetrahydro-2,2,6-trimethyl-
6-Ethenyl-3,4,5,6-tetrahydro-2,2,6-trimethyl-2H-pyran-3-ol
linalool pyran oxide
epoxylinalool (pyranoid)
LINALOOL OXIDE, PYRANOID
FEMA NO. 4593
DTXCID00213173
Linalool oxide pyranoid, (+-)-
2,2,6-trimethyl-6-vinyl tetrahydro-2H-pyran-3-ol
3-hydroxy-2,2,6-trimethyl-6-vinyl tetrahydropyran
6-ethenyl-2,2,6-trimethyl tetrahydro-2H-pyran-3-ol
237-889-1
2,2,6-Trimethyl-6-vinyltetrahydro-2H-pyran-3-ol
6-ethenyl-2,2,6-trimethyloxan-3-ol
2,2,6-Trimethyl-6-vinyltetrahydropyran-3-ol
Linalool oxide pyranoside
MFCD06200770
3-Hydroxy-2,2,6-trimethyl-6-vinyltetrahydropyran
2,6,6-trimethyl-2-vinyl-5-hydroxytetrahydropyran
Cnidiol C
Epoxylinalol
linalool oxide (pyranoid)
UNII-CJQ633A12A
Linalool oxide I (pyranoid)
Linalool oxide pyranoid, (+/-)-
Linalool oxide II (pyranoid)
SCHEMBL309187
(Z)-Linalool oxide (pyranoid)
CHEBI:144708
AKOS006281160
AS-68747
SY052859
CS-0446068
NS00051774
T2605
D92625
6-Ethenyl-tetrahydro-2,2,6-trimethyl-2H-Pyran-3-ol
6-Ethenyltetrahydro-2,2,6-trimethyl-2H-Pyran-3-ol
6-ethenyltetrahydro-2,2,6-trimethyl-2h-pyran-3(4h)-one
linalool oxide C (2,6,6-trimethyl-2-vinyl-5-hydroxytetrahydropyran)