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Geranyl acetate

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Identification
Molecular formula
C12H20O2
CAS number
105-87-3
IUPAC name
3,7-dimethyloct-6-enyl acetate
State
State

Geranyl acetate is typically a liquid at room temperature.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
196.29g/mol
Molar mass
196.2910g/mol
Density
0.8979g/cm3
Appearence

Geranyl acetate is a colorless to pale yellow liquid. It has a sweet, fruity, and floral aroma, reminiscent of roses or lavender, making it a popular choice in the fragrance industry.

Comment on solubility

Solubility of 3,7-Dimethyloct-6-enyl Acetate

3,7-Dimethyloct-6-enyl acetate is an organic compound characterized by its unique structure, which influences its solubility properties. Understanding the solubility of this compound involves considering several key factors:

  • Polarity: The presence of an acetate group tends to enhance polarity, yet the long hydrophobic carbon chain can contribute to hydrophobic characteristics, suggesting that it may be soluble in non-polar solvents.
  • Solvent Compatibility: This compound is likely to be soluble in organic solvents such as ether, hexane, and chloroform, but less favorable in polar solvents like water.
  • Temperature Effects: Like many organic esters, solubility may increase with temperature, making it essential to consider the temperature of the solvent for optimal solubility.

Overall, while 3,7-dimethyloct-6-enyl acetate shows a tendency towards solubility in non-polar organic solvents, its limited solubility in polar solvents underlines the importance of solvent choice in applications involving this compound. In summary, it’s crucial to consider both the chemical structure and the medium when discussing the solubility of this compound.

Interesting facts

Interesting Facts about 3,7-Dimethyloct-6-enyl Acetate

3,7-Dimethyloct-6-enyl acetate, commonly known in the field of chemistry for its intriguing structural properties and applications, will captivate your interest through its versatile characteristics:

  • Natural Affinity: This compound is often found in essential oils, contributing to the aroma and flavor profiles in various plants. Its presence enriches the sensory experience of natural products.
  • Synthetic Pathways: The synthesis of 3,7-dimethyloct-6-enyl acetate can be achieved through various methods, which often include reactions such as esterification and alkylation. This allows researchers to understand and manipulate the reaction pathways for desired outcomes.
  • Flavor and Fragrance: Known for its fruity and sweet scent, this compound is often utilized in the food and cosmetic industries. Its use in flavoring agents and perfumes emphasizes the significance of chemistry in everyday life.
  • Research Implications: The study of this compound is crucial in fields such as organic chemistry and biochemistry, providing insights into molecular interactions, and enhancing the development of new materials and formulations.
  • Environmental Impact: Understanding and studying the degradation of 3,7-dimethyloct-6-enyl acetate in the environment is critical for assessing its ecological footprint and ensuring sustainability in chemical applications.

As an intriguing compound, 3,7-dimethyloct-6-enyl acetate serves as an excellent example of how organic chemistry intersects with nature and industry. It highlights the importance of compounds derived from natural sources and their roles in enhancing human experience through flavor and fragrance. Scientists and students alike can appreciate the multifaceted uses of this compound and its contribution to advancements in various scientific fields.

Synonyms
Citronellyl acetate
150-84-5
Citronellol acetate
3,7-Dimethyloct-6-en-1-yl acetate
3,7-Dimethyl-6-octen-1-yl acetate
Acetic acid, citronellyl ester
3,7-dimethyloct-6-enyl acetate
1-Acetoxy-3,7-dimethyloct-6-ene
6-Octen-1-ol, 3,7-dimethyl-, 1-acetate
Citronellyl ethanoate
3,7-Dimethyl-6-octen-1-ol acetate
2-Octen-8-ol, 2,6-dimethyl-, acetate
6-Octen-1-ol, 3,7-dimethyl-, acetate
FEMA No. 2311
NSC 4893
Ctronellyl acetate (natural)
3,7-Dimethyl-6-octen-1-yl ethanoate
Acetic acid, 3,7-dimethyl-6-octen-1-yl ester
UNII-IZ420RT3OY
EINECS 205-775-0
EINECS 266-837-0
(+/-)-Citronellyl acetate
IZ420RT3OY
BRN 1723886
CHEBI:70478
AI3-02039
beta-citronellol acetate
beta-Citronellyl acetate
NSC-4893
.beta.-Citronellyl acetate
(1)-3,7-Dimethyloct-6-enyl acetate
6-Octen-l-ol, 3,7-dimethyl-, acetate
DTXSID5051739
EC 205-775-0
1-02-00-00065 (Beilstein Handbook Reference)
CITRONELLYL ACETATE, (+/-)-
67650-82-2
MFCD00015039
Cephreine
Cephrol acetate
CitronellyI acetate
DL-Citronellol acetate
.beta.-Citronellol, acetate
SCHEMBL157075
Citronellyl acetate (Standard)
HY-N7144AR
CHEMBL1453648
DTXCID5030294
3,7-Dimethyl-6-octenyl acetate
FEMA 2311
HY-N7144A
CITRONELLYL ACETATE [FCC]
NSC4893
WLN: 1Y1&U3Y1&WOV1
CITRONELLYL ACETATE [FHFI]
MSK40227
BDBM50037054
s5827
2-Octen-8-ol,6-dimethyl-, acetate
6-Octen-1-ol,7-dimethyl-, acetate
AKOS015899521
FC32109
LMPR0102010015
Citronellyl acetate, analytical standard
Citronellyl acetate, >=95%, FCC, FG
NCGC00095623-01
1ST40227
AS-63841
Acetic acid,7-dimethyl-6-octen-1-yl ester
DB-043064
CS-0099257
NS00002234
D89326
Q27138814
205-775-0