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Hexyl octanoate

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Identification
Molecular formula
C14H28O2
CAS number
6378-65-0
IUPAC name
hexyl octanoate
State
State

At room temperature, hexyl octanoate is a liquid. It remains stable under normal conditions of storage and handling.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
242.37g/mol
Molar mass
242.4040g/mol
Density
0.8728g/cm3
Appearence

Hexyl octanoate is a colorless to pale yellow liquid with a fruity, pleasant odor reminiscent of pineapple or green banana. It is often used in flavors and fragrances due to its agreeable scent.

Comment on solubility

Solubility of Hexyl Octanoate

Hexyl octanoate, with the chemical formula C14H28O2, is an ester compound that exhibits interesting solubility characteristics due to its hydrophobic nature.

Key Points on Solubility:

  • Solvent Preferences: Hexyl octanoate is typically soluble in organic solvents such as ethanol, ether, and chloroform.
  • Water Solubility: This compound has a very low solubility in water; this is common for long-chain esters, which are generally insoluble in polar solvents.
  • Temperature Effects: As with many organic compounds, increased temperature can slightly enhance solubility in organic solvents.
  • Applications: Its solubility properties make hexyl octanoate useful in fragrance formulations and as a flavoring agent.

In summary, hexyl octanoate's solubility traits highlight its role in both industrial applications and its limitations when interacting with polar solvents. Understanding these aspects is crucial for effective utilization in various chemical processes.

Interesting facts

Interesting Facts about Hexyl Octanoate

Hexyl octanoate, also known as hexyl caprylate, is an ester formed from the reaction of hexanol and octanoic acid. This compound has garnered attention in both the chemical and consumer product industries due to its unique properties and applications. Here are some fascinating points about hexyl octanoate:

  • Natural Aromatics: This compound contributes a pleasant fruity fragrance, reminiscent of tropical fruits, making it a popular choice in the fragrance and flavoring industries.
  • Casual Applications: Hexyl octanoate can be found in various commercial products such as perfumes, cosmetics, and food flavorings, enhancing their sensory appeals.
  • Solvency Power: Due to its ester structure, hexyl octanoate exhibits excellent solvency properties, allowing it to dissolve a wide range of organic materials, which is beneficial in formulations.
  • Potential in Research: Research into esters like hexyl octanoate has revealed insights into their behavior in the environment, including their effects on ecological systems when released.
  • Creative Synthesis: The synthesis of hexyl octanoate often involves methods such as Fischer esterification, showcasing the versatility of organic reactions in producing valuable compounds.

In summary, hexyl octanoate not only serves functional roles in everyday products but also exemplifies the beauty of organic chemistry through its synthesis and applications. As noted by one researcher, “The world of esters opens up a plethora of sensory experiences that connect chemistry with our daily lives.”

Synonyms
Hexyl octanoate
Hexyl caprylate
n-Hexyl caprylate
OCTANOIC ACID, HEXYL ESTER
Hexyl octylate
FEMA No. 2575
Hexyl octanoate (natural)
FEMA 2575
Caproyl caprylate
EINECS 214-247-9
UNII-GU3S7YK802
BRN 1769635
GU3S7YK802
DTXSID8047636
CHEBI:87490
AI3-33727
N-HEXYL-N-OCTANOATE
HEXYL OCTANOATE [FHFI]
DTXCID6027636
WE(6:0/8:0)
3-02-00-00794 (Beilstein Handbook Reference)
8-(5-Hexyl-furan-2-yl)-octanoate
Hexyl octylic acid
Hexyl caprylic acid
Hexyl octanoic acid
214-247-9
pbgwnxwncssxco-uhfffaoysa-n
1117-55-1
OCTANOIC ACID HEXYL ESTER
MFCD00048920
starbld0009580
Fema2575
Hexyl octanoate, >=97%
SCHEMBL310160
CHEMBL3182596
Tox21_302578
LMFA07010448
AKOS015839915
NCGC00256630-01
AS-56679
CAS-1117-55-1
CS-0451191
NS00012617
D95774
Q27159666