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Geranyl acetate

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Identification
Molecular formula
C12H20O2
CAS number
105-87-3
IUPAC name
(2-isopropenyl-5-methyl-hex-4-enyl) acetate
State
State

At room temperature, geranyl acetate is in a liquid state. Due to its liquid form and pleasant fragrance, it is popularly used in the creation of perfumes and flavorings, contributing to various aromatic profiles.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
236.00
Boiling point (Kelvin)
509.15
General information
Molecular weight
196.29g/mol
Molar mass
196.2940g/mol
Density
0.9080g/cm3
Appearence

Geranyl acetate is a clear, colorless to pale yellow liquid. It has a pleasant floral or fruity odor, which is commonly associated with sweet, rose-like, fruity scents often used in perfumery and flavorings.

Comment on solubility

Solubility of (2-isopropenyl-5-methyl-hex-4-enyl) acetate

When exploring the solubility of (2-isopropenyl-5-methyl-hex-4-enyl) acetate, we discover some intriguing characteristics that define its behavior in various solvents. Generally, solubility is influenced by several factors including molecular structure, size, polarity, and the nature of the solvent. In the case of this compound, its distinct structure suggests:

  • Moderate Polarity: The presence of the ester functional group contributes a degree of polarity which can enhance solubility in polar solvents.
  • Hydrophobic Characteristics: The long hydrocarbon chain may limit solubility in highly polar solvents like water but can still dissolve in less polar or non-polar solvents.
  • Solvent Compatibility: It is likely to demonstrate good solubility in organic solvents such as ethanol, ethyl acetate, and hexane.

As with many organic compounds, temperature and pressure can also play significant roles in solubility. Typically:

  • Increasing temperature can enhance solubility in many solvents.
  • Increased pressure may affect gases more significantly than liquids but can still have an impact based on molecular interactions.

In summary, while (2-isopropenyl-5-methyl-hex-4-enyl) acetate may not dissolve readily in water due to its hydrophobic characteristics, it holds promise for good solubility in various organic solvents, illustrating the complex interplay of molecular features in determining solubility.

Interesting facts

Interesting Facts About (2-isopropenyl-5-methyl-hex-4-enyl) Acetate

(2-isopropenyl-5-methyl-hex-4-enyl) acetate, often referred to in research and industry for its unique structure and applications, presents a fascinating case for chemical study. Here are some noteworthy points regarding this compound:

  • Derivative of Natural Compounds: This compound is a derivative of naturally occurring substances, often used in fragrances and flavorings, due to its pleasant aroma.
  • Versatile Applications: Its structure allows it to be a precursor for various synthetic pathways, enhancing its utility in organic synthesis.
  • Significant in Aromatherapy: (2-isopropenyl-5-methyl-hex-4-enyl) acetate is recognized for its potential roles in aromatherapy, contributing to the therapeutic qualities of essential oils.

Chemical Structure Insights

The compound's structure features a complex arrangement of carbon atoms, providing multiple points of reactivity. The presence of double bonds enhances its reactivity, making it suitable for various chemical transformations:

  • Geometric Isomerism: The presence of double bonds allows for geometric isomerism, which can result in different physical and chemical properties.
  • Functional Groups: Its acetate functional group plays a crucial role in its reactivity, particularly in esterification reactions.

Biological Implications

Research has shown that compounds like (2-isopropenyl-5-methyl-hex-4-enyl) acetate may possess biological activities, including:

  • Antimicrobial Properties: Studies suggest that such compounds could have antimicrobial effects, making them of interest in pharmacology.
  • Potential as a Repellent: There is ongoing investigation into its use as a natural repellent against pests, reflecting its ecological applications.

In summary, (2-isopropenyl-5-methyl-hex-4-enyl) acetate exemplifies the diverse roles chemical compounds can play in both nature and industry. Its unique structure makes it a compound of interest in research, with potential for various applications in fields such as aromatherapy, organic synthesis, and pharmacology.

Synonyms
Lavandulyl acetate
25905-14-0
(+/-)-Lavandulyl acetate
acetic acid lavandulyl ester
(R)-Lavandulyl acetate
MFCD16652611
(5-methyl-2-prop-1-en-2-ylhex-4-enyl) acetate
(-)-Lavandulyl acetate
4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, 1-acetate
OU6ZF37MOM
4-HEXEN-1-OL, 5-METHYL-2-(1-METHYLETHENYL)-, ACETATE
2-Isopropenyl-5-methylhex-4-enyl acetate
2-Isopropenyl-5-methyl-4-hexen-1-yl acetate
3-Acetoxymethyl-2,6-dimethyl-1,5-heptadiene
5-METHYL-2-(PROP-1-EN-2-YL)HEX-4-EN-1-YL ACETATE
4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, acetate, (2R)-
( inverted exclamation markA)-Lavandulyl acetate
4-Hexen-1-ol, 2-isopropenyl-5-methyl-, acetate
5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol acetate
(-)-(R)-Lavandulyl acetate
EINECS 244-026-2
UNII-OU6ZF37MOM
(+-)-Lavandulol acetate
(+-)-Lavandulyl acetate
(R)-2-Isopropenyl-5-methylhex-4-enyl acetate
EINECS 247-327-7
4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, acetate, (R)-
(??)-Lavandulyl Acetate
(2-isopropenyl-5-methyl-hex-4-enyl) acetate
(+/-)-Lavandulol acetate
SCHEMBL132576
5-Methyl-2-(1-propen-2-yl)-4-hexen-1-yl Acetate
ACETICACIDLAVANDULYLESTER
(+/-)-2-Isopropenyl-5-methyl-4-hexen-1-yl acetate
orb1679987
DTXSID30904865
(R)-Lavandulyl acetate; (-)-Lavandulyl acetate; (-)-(R)-Lavandulyl acetate;
AKOS032957243
LAVANDULYL ACETATE, (+/-)-
HY-117419A
FL161233
SY319471
DB-253441
CS-0253678
NS00012786
E80382
Q16948466
5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol 1-acetate
(+/-)-2-Isopropenyl-5-methyl-4-hexen-1-yl acetate;(+/-)-Lavandulol acetate