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Linalyl formate

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Identification
Molecular formula
C12H20O2
CAS number
17352-13-3
IUPAC name
[1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl] formate
State
State
Linalyl formate is a liquid at room temperature. It is often used in the fragrance industry, highlighting its role as an essential oil component.
Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
196.29g/mol
Molar mass
168.2590g/mol
Density
0.8950g/cm3
Appearence
Linalyl formate is typically a colorless to pale yellow liquid. It has a pleasant floral odor and is often described as having a trace of bergamot and lavender-like scent, making it useful in perfumery and flavoring applications.
Comment on solubility

Solubility of [1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl] formate

[1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl] formate, a compound with a complex structure, exhibits unique solubility properties that can be influenced by various factors. The solubility of this compound is primarily dependent on its molecular interactions with solvents. Here are some key points to consider:

  • Polarity: The presence of polar functional groups, such as the formate group, suggests that this compound may have some degree of polarity, allowing it to dissolve in polar solvents.
  • Hydrophobic Nature: The bulky cyclohexene ring may impart a hydrophobic character, potentially limiting its solubility in water while promoting solubility in organic solvents.
  • Solvent Compatibility: Compatible solvents for [1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl] formate are likely to include:
    • Alcohols, such as ethanol or methanol
    • Diethyl ether
    • Aromatic hydrocarbons, like toluene
  • Temperature Effects: Increased temperature typically enhances solubility for many organic compounds, making warmer solvents more effective at dissolving this compound.

In conclusion, the solubility of [1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl] formate is influenced by both its structural attributes and the nature of the solvent. Understanding these interactions is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts about 1-Methyl-1-(4-Methylcyclohex-3-en-1-yl)ethyl Formate

1-Methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl formate is a fascinating compound from the perspective of a chemist, particularly because of its intriguing structural features and potential applications. This compound belongs to a class of esters, which are well-known for their pleasant fragrances and roles in flavors and fragrances.

Key Characteristics

  • Structural Diversity: The presence of both a methyl group and a cyclohexene ring adds to the complexity of its structure, leading to unique reactivity and interactions.
  • Potential Uses: Esters are often associated with fruity aromas, making this compound a candidate for flavoring agents in the food industry, as well as in perfumes and scented products.
  • Synthetic Pathways: The synthesis of this compound can involve interesting organic reactions, offering students and chemists alike an opportunity to explore esterification and alkylation processes.

As with many organic compounds, the study of 1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl formate can lead to a deeper understanding of:

  • Reactivity patterns in organic chemistry
  • Mechanisms of flavor and fragrance formation
  • Applications in medicinal chemistry, especially if derivatives are explored

Understanding the properties and applications of compounds like 1-methyl-1-(4-methylcyclohex-3-en-1-yl)ethyl formate showcases the intersection of chemistry with everyday life. As we delve deeper into the fascinating world of organic compounds, we continuously uncover the **dynamic roles** they play in various industries, reflecting the creativity and utility of chemical science. As a quote from the renowned chemist Linus Pauling reminds us, "The best way to have a good idea is to have a lot of ideas." This sentiment underscores the importance of exploration and experimentation in the world of chemistry!

Synonyms
Terpinyl formate
2153-26-6
p-1-Menthen-8-yl formate
alpha-Terpinyl formate
P-Menth-1-en-8-yl formate
FEMA No. 3052
P-Menth-1-en-8-ol, formate
p-menth-1-en-8-yl-formate
GTJ0954O31
EINECS 218-444-0
alpha,alpha,4-Trimethyl-3-cyclohexene-1-methyl formate
TERPINYL FORMATE [FHFI]
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, formate
.ALPHA.-TERPINYL FORMATE
DTXSID20862849
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, formate
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-formate
3-CYCLOHEXENE-1-METHANOL, .ALPHA.,.ALPHA.,4-TRIMETHYL-, 1-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, 1-formate
DTXCID00219519
TERPENOL FORMATE, (+-)-
.ALPHA.-TERPINYL FORMATE, (+-)-
P-MENTH-1-EN-8-OL, FORMATE, (+-)-
3-CYCLOHEXENE-1-METHANOL, ALPHA,ALPHA,4-TRIMETHYL-, 1-
3-CYCLOHEXENE-1-METHANOL,,ALPHA.,.ALPHA.,4-TRIMETHYL-, 1-FORMATE, (+-)-
3-CYCLOHEXENE-1-METHANOL,,ALPHA.,ALPHA,4-TRIMETHYL-, 1-FORMATE, (+-)-
2-(4-methylcyclohex-3-en-1-yl)propan-2-yl formate
alpha-Terpineol formate
TERPINYLFORMATE
a-Terpineol formate
SCHEMBL561372
UNII-GTJ0954O31
CHEMBL4162810
FEMA 3052
CHEBI:168454
TERPENOL FORMATE, (+/-)-
DB-045610
.ALPHA.-TERPINYL FORMATE, (+/-)-
NS00013200
P-MENTH-1-EN-8-OL, FORMATE, (+/-)-
2-(4-methylcyclohex-3-en-1-yl)propan-2-yl ormate
Q27279272
1-Methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl formate #
3-CYCLOHEXENE-1-METHANOL, ,ALPHA.,.ALPHA.,4-TRIMETHYL-, 1-FORMATE, (+/-)-