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Linalyl acetate

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Identification
Molecular formula
C12H20O2
CAS number
115-95-7
IUPAC name
(1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate
State
State

At room temperature, linalyl acetate is a liquid. It is well-known for its volatility and aromatic properties, making it valuable in the production of fragrances and flavorings.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
220.50
Boiling point (Kelvin)
493.60
General information
Molecular weight
196.29g/mol
Molar mass
196.2940g/mol
Density
0.9030g/cm3
Appearence

Linalyl acetate is a colorless to pale yellow liquid with a pleasant floral odor, reminiscent of lavender and bergamot. It is commonly used in perfumery and flavoring.

Comment on solubility

Solubility of (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate

The solubility of the compound (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate can be influenced by several factors, primarily due to its structural characteristics. As an acetate, this compound tends to display unique polarity dynamics that can affect its solubility in different solvents.

Factors Affecting Solubility

  • Polarity: The presence of the acetate functional group generally contributes to hydrophilicity, yet the bulkiness of the isopropyl and methyl groups can hinder solubility in polar solvents.
  • Solvent Type: It is likely to be more soluble in organic solvents such as ethanol, acetone, and ethyl acetate, while exhibiting limited solubility in water.
  • Temperature: Like many organic compounds, an increase in temperature may enhance solubility, as molecular movements become more vigorous at higher temperatures.

In summary, while (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate can exhibit varying degrees of solubility depending on the medium, it is essential to consider its structural attributes that contribute to its behavior in different solvent environments. As the saying goes, "like dissolves like," which remains a fundamental principle in predicting solubility.

Interesting facts

Interesting Facts about (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) Acetate

(1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate is a fascinating compound that's often scrutinized within the fields of organic chemistry and perfumes. Here are some compelling insights into this intriguing substance:

  • Structure and Stability: The compound features a cyclohexene ring, which contributes to its unique reactivity profile. The double bond within the ring provides sites for chemical reactions, making it an important structure for synthesized compounds.
  • Floral Notes: This acetate variant is known for imparting sweet, floral aromas, which often find applications in the fragrance industry. It’s frequently used in perfumes and flavoring agents, enhancing scents and tastes with its pleasant properties.
  • Source of Natural Compounds: (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate can be derived from several natural essential oils, linking it to fragrances found in plants and flowers. Such connections can make it particularly appealing for those interested in natural product chemistry.
  • Reactivity: The presence of the acetate functional group makes the compound susceptible to hydrolysis, allowing it to break down into its constituent parts in the presence of water. This demonstrates the dynamic nature of organic compounds.
  • Use in Synthesis: In synthetic organic chemistry, derivatives like this acetate can serve as intermediates or building blocks in the creation of more complex molecules, showcasing the versatility and importance of such compounds in both industrial and academic settings.

In summary, (1-isopropyl-4-methyl-cyclohex-3-en-1-yl) acetate not only holds significance in fragrance creation but also serves as a remarkable example of how organic compounds can intersect with nature, chemistry, and industrial applications. Scientists continuously explore its properties and potential, making it a compound of ongoing interest.

Synonyms
Terpinene 4-acetate
4-Terpinyl acetate
4-TERPINENYL ACETATE
4821-04-9
(4-methyl-1-propan-2-ylcyclohex-3-en-1-yl) acetate
3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, acetate
4-Terpineol acetate
p-Menth-1-en-4-ol, acetate
1-Terpinen-4-ol acetate
3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, 1-acetate
302N85584M
1-TERPINEN-4-YL ACETATE
DTXSID90884114
EINECS 225-395-9
(4,6,6-trimethyl-3-(2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo(3.1.1)hept-1-enyl)-3-bicyclo(3.1.1)hept-1-enyl)-2-bicyclo(3.1.1)hept-4-enyl) acetate
[4,6,6-trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]-2-bicyclo[3.1.1]hept-4-enyl] acetate
DTXCID001023584
terpinen-4-ol acetate
1-(Isopropyl)-4-methylcyclohex-3-en-1-yl acetate
Terpin-4-yl acetate
Terpinen-4-yl acetate
Terpinene-4-yl acetate
Terpinen-4-ol, acetate
SCHEMBL9951564
CHEBI:184320
UNII-302N85584M
(+/-)-TERPINENE 4-ACETATE
TERPINENE 4-ACETATE, (+/-)-
NS00047224
1-Isopropyl-4-methyl-3-cyclohexen-1-yl acetate #
Q27255896
1-ISOPROPYL-4-METHYLCYCLOHEX-3-EN-1-YL ACETATE