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Octyl acetate

Octyl acetate
Skeletal formula of octyl acetate
Names
IUPAC name
Octyl acetate
Other names
Octyl ethanoate
n-Octyl acetate
Identifiers
112-14-1 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:87495 YesY
ChemSpider 7872 YesY
ECHA InfoCard 100.003.581
PubChem 8164
RTECS number AJ1400000
Properties
C10H20O2
Molar mass 172.27 g·mol−1
Appearance Colorless liquid
Odor Fruity, slightly waxy floral odor
Density 0.863–0.87 g/cm3
Melting point −38.5 – −38 °C (−37.3 – −36.4 °F; 234.7–235.2 K)
Boiling point 203–211.3 °C (397.4–412.3 °F; 476.1–484.4 K)
112.55 °C (234.59 °F; 385.70 K)
at 30 mmHg
0.021 g/100 g (0 °C)
0.018 g/100 g (29.7 °C)
0.018 g/100 g (40 °C)
0.012 g/100 g (92.1 °C)
Solubility Soluble in EtOH, ether
Vapor pressure 0.01 kPa (−3 °C)
0.0072–0.0073 (14.75 °C)
0.02–0.1 kPa (27 °C)
1 kPa (66.3 °C)
10 kPa (120 °C)
1.415–1.422 (20 °C)
Thermochemistry
331–343.74 J/mol·K
Hazards
NFPA 704
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g., diesel fuel Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 83–86 °C (181–187 °F; 356–359 K)
268–268.3 °C (514.4–514.9 °F; 541.1–541.5 K)
Explosive limits 0.76–8.14%
Lethal dose or concentration (LD, LC):
LD50 (median dose)
3000 mg/kg (oral, rat)
5000 mg/kg (dermal, rabbit)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY  (what is YesYN ?)
Infobox references

Octyl acetate, or octyl ethanoate, is an organic compound with the formula CH3(CH2)7O2CCH3. It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products.

Octyl acetate can be synthesized by a condensation of 1-octanol and acetic acid:

Because of its fruity odor, octyl acetate is used as the basis for artificial flavors and in perfumery. It is also a solvent for nitrocellulose, waxes, oils, and some resins.


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