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Linalyl propionate

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Identification
Molecular formula
C13H22O2
CAS number
144-39-8
IUPAC name
(5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate
State
State

At room temperature, linalyl propionate is typically a liquid. This state facilitates its use in various applications such as fragrances and flavorings.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
222.00
Boiling point (Kelvin)
495.15
General information
Molecular weight
196.32g/mol
Molar mass
196.2910g/mol
Density
0.9470g/cm3
Appearence

Linalyl propionate appears as a colorless to pale yellow liquid. It possesses a fragrant aroma, characteristic of fresh and fruity notes, often used in perfumery to impart a sweet and floral scent with a hint of fruitiness.

Comment on solubility

Solubility of (5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate

(5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate is a complex organic compound that exhibits interesting solubility characteristics. Solubility can be influenced by various factors including polarity, molecular structure, and the presence of functional groups. Here are some key points regarding its solubility:

  • Polarity: The presence of the propanoate functional group lends a degree of polarity to the molecule, allowing it to be more soluble in polar solvents compared to its non-polar counterparts.
  • Solvent Compatibility: It may be soluble in organic solvents such as ethanol, acetone, and chloroform due to its non-polar hydrocarbon structure intertwined with a polar ester group.
  • Temperature Influence: Like many organic compounds, solubility can vary with temperature; an increase in temperature typically enhances the solubility of solids in liquids.
  • Hydrophobic Effects: The hydrophobic parts of the molecule might limit its solubility in water, thus making it relatively insoluble in aqueous solutions.
  • Applications: Its solubility properties make it suitable for various applications, including its use in fragrances and flavorings where solubility is crucial.

In conclusion, while (5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate shows potential for solubility in organic solvents, the complex interplay of its molecular structure and the nature of the solvent largely determines the extent of its solubility. As noted, “Like dissolves like,” highlighting the importance of choosing the right solvent for effective dissolution.

Interesting facts

Interesting Facts about (5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate

(5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate is a fascinating compound that exemplifies the diversity of organic chemistry. Known for its unique structural features, this compound belongs to a class of compounds known as esters, which are renowned for their pleasant fragrances and flavors.

Key Characteristics

  • Esters in Nature: Esters are commonly found in nature, contributing to the smell and taste of many fruits. This specific ester may evoke similar aromatic properties.
  • Versatile Applications: Compounds like (5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate are often utilized in the food and fragrance industries due to their ability to impart desirable characteristics to products.
  • Potential Medicinal Uses: The unique structure of this compound may open avenues for potential medicinal applications, particularly in the area of anti-inflammatory or antimicrobial agents.
  • Polymerization Opportunities: The presence of the isopropenyl group makes it a candidate for polymerization reactions, leading to materials with varied properties.

Moreover, studying such compounds enhances our understanding of chemical reactivity and the principles that govern organic synthesis. As one researcher notes, "The beauty of organic chemistry lies in its ability to create complexity from simplicity." This highlights the potential for synthesizing a wide variety of derivatives and related compounds from the parent structure.

In conclusion, (5-isopropenyl-2-methyl-cyclohex-2-en-1-yl) propanoate not only showcases the intricacies of organic compounds but also their relevance in everyday life and potential applications across multiple fields. Its study can inspire both current and future chemists to explore the vast possibilities within organic chemistry.

Synonyms
Carvyl propionate
97-45-0
Carvyl propioate
Carveol propionate
l-Carvyl propionate
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, propanoate
p-MENTHA-6,8-DIEN-2-OL, PROPIONATE
p-Mentha-1(6),8-dien-2-yl propionate
p-Mentha-6,8-dien-2-yl propionate
(-)-Carvyl propioate
l-p-Mentha-6,8(9)-dien-2-yl propionate
2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl propanoate
2-Methyl-5-(1-methylethenyl)-2-cyclohexenyl propanoate
Carvyl propionate, (+/-)-
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, propionate
DTXSID30861702
TW615E88E9
2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl propionate
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, 1-propanoate
(-)-Carvyl propionate
FEMA No. 2251
EINECS 202-583-9
BRN 2526499
UNII-TW615E88E9
AI3-26372
5-Isopropenyl-2-methyl-2-cyclohexen-1-yl propionate #
SCHEMBL891525
FEMA 2251
DTXCID80810588
(2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-yl) propanoate
(-)-Carvyl propionate, >=97%
AKOS015913534
(-)-Carvyl propionate mixture of isomers
NS00012079
G84020
5-Isopropenyl-2-methyl-2-cyclohexen-1-yl propionate
2-Cyclohexen-1-ol,2-methyl-5-(1-methylethenyl)-,1-propanoate