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Linalyl acetate

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Identification
Molecular formula
C12H22O2
CAS number
115-95-7
IUPAC name
(2-isopropyl-5-methyl-cyclohexyl) acetate
State
State

At room temperature, linalyl acetate is a liquid. It is typically not very viscous and flows easily.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.20
Boiling point (Celsius)
220.50
Boiling point (Kelvin)
493.70
General information
Molecular weight
198.30g/mol
Molar mass
198.3000g/mol
Density
0.9394g/cm3
Appearence

Linalyl acetate is a colorless liquid with a sweet floral fragrance, reminiscent of lavender. It is often used in perfumes and essential oils for its pleasant aroma.

Comment on solubility

Solubility of (2-isopropyl-5-methyl-cyclohexyl) acetate

(2-isopropyl-5-methyl-cyclohexyl) acetate, a compound with a complex structure, showcases intriguing solubility characteristics that can be influenced by various factors.

Generally, the solubility of organic compounds like this one can be described with reference to the following key points:

  • Polarity: The presence of the acetate functional group contributes to *moderate polarity*, which can enhance solubility in polar solvents.
  • Hydrophobic Character: The cyclohexyl moiety is relatively hydrophobic, suggesting that (2-isopropyl-5-methyl-cyclohexyl) acetate may exhibit greater solubility in non-polar organic solvents.
  • Temperature Dependency: Like many organic compounds, solubility is often *temperature dependent*. Higher temperatures typically increase the solubility of solids and certain liquids in solvents.
  • Solvent Effects: This compound is likely to be soluble in solvents such as ethanol, ether, and possibly some aromatic hydrocarbons, while being less soluble in water due to its hydrophobic elements.

As a general observation, the combined effect of its polar and non-polar regions makes (2-isopropyl-5-methyl-cyclohexyl) acetate a compound that can exhibit variable solubility depending on the solvent used. Therefore, it is crucial for chemists and researchers to consider the specific solvent characteristics in study and application contexts.

Interesting facts

Interesting Facts About (2-Isopropyl-5-methyl-cyclohexyl) Acetate

(2-Isopropyl-5-methyl-cyclohexyl) acetate is a fascinating compound that belongs to the family of esters. Esters are widely known for their pleasant fragrances and are commonly featured in flavorings and perfumes. This specific compound is noteworthy for several reasons:

  • Fragrance Profile: It is often associated with fruity and floral notes, making it a potential candidate for use in the fragrance industry.
  • Versatile Applications: Beyond scents, it can be utilized as a solvent in various applications, enhancing the performance of paints and coatings.
  • Synthetic Pathways: The synthesis of (2-isopropyl-5-methyl-cyclohexyl) acetate involves interesting chemical reactions, commonly using acetic acid and specific alcohols, which allows for the exploration of different cheminformatics methodologies.
  • Natural Occurrence: Compounds similar to this acetate can be found naturally in various plants and fruits, contributing to their aroma and flavor, thus playing a role in essential oil production.

This compound provides an excellent opportunity for students and researchers alike to explore concepts such as esterification, molecular interaction, and application in everyday products. As you delve into its study, consider not only the chemical reactions involved in its creation but also its role in enhancing our sensory experiences through scent and flavor.

In conclusion, (2-Isopropyl-5-methyl-cyclohexyl) acetate stands as a fascinating compound that intersects chemistry and sensory perception, making it a rewarding topic for exploration in the field of organic chemistry.

Synonyms
Menthyl acetate
16409-45-3
89-48-5
Menthol, acetate
Menthyl acetate racemic
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate
29066-34-0
2230-87-7
(5-methyl-2-propan-2-ylcyclohexyl) acetate
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate, (1R,2S,5R)-rel-
(1R)-(-)-Menthyl acetate
(2-isopropyl-5-methyl-cyclohexyl) acetate
d-Neomenthyl acetate
2-Isopropyl-5-methylcyclohexyl acetate
5-Methyl-2-(1-methylethyl)cyclohexanol acetate
Neomenthol acetate
FEMA Number 2668
L-Menthyl acetate;(-)-Menthyl acetate
HSDB 824
(.+/-.)-Menthol acetate
EINECS 240-459-6
(1R,2S,5R)-rel-2-Isopropyl-5-methylcyclohexyl acetate
Acetic acid, p-menth-3-yl ester, dl-
enthyl acetate
AI3-36197
Menthol, neo-
CYCLOHEXANOL, 5-METHYL-2-(1-METHYLETHYL)-, ACETATE, (1.ALPHA.,2.BETA.,5.ALPHA.)-
Menthyl Acetate; Cyclohexanol, 5-methyl-2-(1-methylethyl)-, 1-acetate (ACI); Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate (9CI); Menthol, acetate (6CI, 8CI); 2-Isopropyl-5-methylcyclohexyl acetate; Acetic acid 5-methyl-2-(1-methylethyl)cyclohexyl es
EINECS 218-767-7
Acetate de menthanyle
(5R)-2-Isopropyl-5-methylcyclohexyl acetate
starbld0011430
Menthyl acetate, 97%
acetic acid menthyl ester
[(1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl] acetate
SCHEMBL57396
CHEMBL254585
SCHEMBL7732630
2-Isopropyl-5-methylcyclohexyl acetate, (1.alpha.,2.beta.,5.alpha.)-
SCHEMBL10401812
DTXSID20859153
NSC7350
Acetic acid, p-menth-3-yl ester
CHEBI:191550
HMS5085C03
NSC-7350
RAA40945
DL-Menthyl acetate, >=97%, FG
L-enthyl acetate;(-)-enthyl acetate
MSK014185
NSC122112
AKOS015837885
NSC 122112
NSC-122112
SB44841
SB46743
AS-83629
DB-063670
DB-071375
5-methyl-2-(propan-2-yl)cyclohexyl acetate
NS00077576
Cyclohexanol, acetate, (1.alpha.,2.alpha.,5.beta.)-
Menthyl acetate, primary pharmaceutical reference standard
Cyclohexanol, acetate, [1S-(1.alpha.,2.alpha.,5.beta.)]-
Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate, (1.alpha.,2.beta.,5.alpha.)-(.+/-.)-
InChI=1/C12H22O2/c1-8(2)11-6-5-9(3)7-12(11)14-10(4)13/h8-9,11-12H,5-7H2,1-4H