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Menthone

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Identification
Molecular formula
C10H18O
CAS number
14073-97-3
IUPAC name
6-isopropyl-3-methyl-cyclohex-2-en-1-one
State
State

Menthone is a liquid at room temperature, though it may solidify under cooler conditions.

Melting point (Celsius)
-4.00
Melting point (Kelvin)
269.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
0.8992g/cm3
Appearence

Menthone is a colorless or pale yellow liquid with a characteristic minty odor. It is often found in essential oils and can solidify at lower temperatures into crystals.

Comment on solubility

Solubility of 6-isopropyl-3-methyl-cyclohex-2-en-1-one

The solubility of 6-isopropyl-3-methyl-cyclohex-2-en-1-one, a complex organic compound, can be influenced by several factors, primarily due to its unique structure. Here are some insights regarding its solubility characteristics:

  • Polarity: The presence of a cyclohexenone structure typically increases the compound's hydrophobic nature, making it less soluble in polar solvents like water.
  • Organic Solvents: Compounds with similar chemical structures are generally more soluble in organic solvents such as:
    • Ether
    • Benzene
    • Chloroform
  • Temperature: Solubility can be highly temperature-dependent; increased temperatures often enhance solubility in organic solvents.
  • Miscibility: It’s essential to note that while it may dissolve well in organic solvents, it could have limited miscibility with water, which is typical for alkyl-substituted compounds.

In conclusion, studying the solubility of 6-isopropyl-3-methyl-cyclohex-2-en-1-one is crucial for applications in organic synthesis and industrial uses, particularly in the formulation of products that require specific solubility characteristics. Understanding the solubility behavior can lead to better utilization in various chemical processes.

Interesting facts

Interesting Facts about 6-Isopropyl-3-methyl-cyclohex-2-en-1-one

6-Isopropyl-3-methyl-cyclohex-2-en-1-one is a fascinating compound that presents several intriguing aspects, particularly in the realm of organic chemistry and its applications. Here are some key points:

  • Structure and Reactivity: This compound features a unique bicyclic structure, contributing to its distinct chemical reactivity. The presence of the unsaturated carbonyl group makes it a valuable intermediate in organic synthesis.
  • Synthetic Applications: Due to its functional groups, 6-isopropyl-3-methyl-cyclohex-2-en-1-one can be utilized in the synthesis of various complex molecules. It often serves as a building block in the creation of natural products and pharmaceutical agents.
  • Flavor and Fragrance: Compounds with similar structures are frequently explored in the flavor and fragrance industries. They can impart unique aromas and tastes, enhancing food products and perfumes.
  • Biological Activity: While specific biological studies on this compound may be limited, its structural relatives often exhibit interesting biological properties, including antimicrobial and antifungal activities, making them subjects of ongoing research.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” This maxim resonates in the study of 6-isopropyl-3-methyl-cyclohex-2-en-1-one, as it encourages chemists to explore the vast potential of this compound in various fields, from medicinal chemistry to industrial applications.

Exploring the intricate details of compounds like 6-isopropyl-3-methyl-cyclohex-2-en-1-one not only enhances our understanding of organic chemistry but also opens doors to innovative solutions in various scientific disciplines.

Synonyms
PIPERITONE
89-81-6
p-Menth-1-en-3-one
3-Carvomenthenone
6-Isopropyl-3-methylcyclohex-2-enone
2-Cyclohexen-1-one, 3-methyl-6-(1-methylethyl)-
3-methyl-6-(propan-2-yl)cyclohex-2-en-1-one
1-Methyl-4-isopropyl-1-cyclohexen-3-one
3-methyl-6-propan-2-ylcyclohex-2-en-1-one
DL-Piperitone
EINECS 201-942-7
(+-)-Piperitone
NSC 251528
3-methyl-6-(1-methylethyl)-2-cyclohexen-1-one
BRN 1907772
1VZ8RG269R
CHEBI:48933
AI3-16053
PIPERITONE [MI]
PIPERITONE, DL-
MFCD00045532
NSC-251528
DTXSID7052604
EC 201-942-7
2-07-00-00075 (Beilstein Handbook Reference)
FEMA NO. 2910, DL-
6-Isopropyl-3-methyl-2-cyclohexen-1-one
6-Isopropyl-3-methyl-2-cyclohexen-1-one predominantly
Piperitone (mixture of enantiomers, predominantly (R)-(-)-form)
UNII-1VZ8RG269R
laevo-piperitone
dextro-piperitone
Piperitone (Standard)
2-Cyclohexen-1-one, dimer
SCHEMBL111913
Piperitone, analytical standard
CHEMBL2252746
DTXCID1031177
FEMA 2910
HY-N9496R
NSC1100
AAA08981
HY-N9496
NSC-1100
NSC176162
NSC251528
6-Isopropyl-3-methyl-2-cyclohexenone
AKOS015840487
NSC-176162
AS-56754
SY105214
DB-057169
6-Isopropyl-3-methyl-2-cyclohexen-1-one #
CS-0181935
NS00006431
P2355
D92155
EN300-174688
Q2041498
201-942-7