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Ethylmaltol

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Identification
Molecular formula
C7H10O3
CAS number
4940-11-8
IUPAC name
2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one
State
State

At room temperature, ethylmaltol is a solid. It is stable under normal conditions, making it easy to handle and use in various applications.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.15
General information
Molecular weight
168.17g/mol
Molar mass
168.1740g/mol
Density
1.0635g/cm3
Appearence

Ethylmaltol appears as a white crystalline powder. It is known for its sweet aroma reminiscent of caramel, making it a common additive in the food industry for flavoring purposes.

Comment on solubility

Solubility of 2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one

The compound 2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one is known to exhibit specific solubility characteristics, primarily influenced by its functional groups and molecular structure. Here are several key points regarding its solubility:

  • Polar Nature: The presence of the hydroxyl (-OH) group contributes to the molecule's polar characteristics, enhancing its solubility in polar solvents such as water.
  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents like ethanol and acetone due to the combination of its nonpolar and polar traits.
  • Temperature Effect: Like many organic compounds, solubility may increase with temperature, allowing for improved dissolution in suitable solvents.
  • Concentration-Dependent Behavior: It is essential to consider that the solubility of 2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one may vary with concentration, potentially leading to saturation limits in various solvents.

In summary, understanding the solubility of this compound is crucial for various applications, including its use in formulations and reactions. This solubility profile emphasizes the importance of carefully selecting solvents for efficient dissolution and practical utilization.

Interesting facts

Interesting Facts about 2-Allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one

This unique compound, known as 2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one, presents a fascinating study in organic chemistry due to its complex structure and various potential applications. Here are some intriguing insights:

  • Natural Occurrence: This compound is related to naturally occurring compounds, particularly found in some essential oils and plant extracts, which contributes to their flavor and aroma profiles.
  • Biological Activity: It has been noted for its potential biological activities, including antimicrobial and antioxidant properties, making it a candidate for healthcare and cosmetic applications.
  • Cyclopentene Derivative: As a cyclopentene derivative, it embodies an interesting twist in cyclic organic compounds, showcasing the versatility of carbon frameworks in forming ring structures.
  • Reactivity: The presence of both allyl and hydroxy functional groups suggests potential reactivity patterns that can be utilized in organic synthesis, making it a valuable intermediate in various chemical reactions.
  • Research Potential: The compound has gained attention in recent research for its potential applications in developing new materials and pharmaceuticals, reflecting the ongoing exploration in organic synthesis.

As scientists continue to investigate and characterize compounds like 2-allyl-4-hydroxy-3-methyl-cyclopent-2-en-1-one, we gain deeper insights into their functional roles and capabilities within biological systems and industry.

In the words of chemist and entrepreneur, "The beauty of chemistry lies in the unseen connections and the exciting possibilities that every molecule holds."

Synonyms
Allethrolone
29605-88-7
Allethrolon
551-45-1
2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propenyl)-
Allethrolone (VAN)
4-hydroxy-3-methyl-2-prop-2-enylcyclopent-2-en-1-one
EINECS 249-724-0
NSC 42192
(1)-2-Allyl-4-hydroxy-3-methylcyclopent-2-en-1-one
AI3-20047
2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-
DTXSID80885458
2-Cyclopenten-1-one, 2-allyl-4-hydroxy-3-methyl-
2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propenyl)-, (+-)-
4-hydroxy-3-methyl-2-(2-propenyl)-2-cyclopenten-1-one
DTXCID901009701
2-Cyclopenten-1-one, 2-allyl-4-hydroxy-3-methyl-(VAN)
2-Cyclopenten-1-one, 2-allyl-4-hydroxy-3-methyl-(VAN) (8CI)
kzyvozabvxlaly-uhfffaoysa-n
2-Allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one
4-Hydroxy-3-methyl-2-(2-propenyl)-2-cyclopentene-1-one
NSC-42192
4-hydroxy-3-methyl-2-prop-2-enyl-cyclopent-2-en-1-one
SCHEMBL358422
8S434R5MLE
4-hydroxy-3-methyl-2-(prop-2-en-1-yl)cyclopent-2-en-1-one
NSC42192
AKOS006272438
2-allyl-3-methyl-4-hydroxy-2cyclopentenone
NS00052325
2-allyl-3-methyl-4-hydroxy-2-cyclopentenone
2-allyl-4-hydroxy-3-methyl-2-cyclopentenone
3-allyl-2-metyl-1-hydroxy-2-cyclopenten-4-one
A819974
2-Allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one #
hydroxy-3-methyl-2-(2-propenyl)-2-cyclopenten-1-one
4-hydroxy-3-methyl-2-prop-2-enyl-1-cyclopent-2-enone
2-Cyclopenten-1-one, 2-allyl-4-hydroxy-3-methyl- (VAN)
3-methyl-4-oxidanyl-2-prop-2-enyl-cyclopent-2-en-1-one
4-Hydroxy-3-methyl-2-(2-propen-1-yl)-2-cyclopenten-1-one
(RS)-3-methyl-2-(2-propenyl)-4-hydroxy-cyclopent-2-ene-1-one
(RS)-4-hydroxy-3-methyl-2-(2-propenyl)-cyclopent-2-ene-1-one