Isoamyl acetate

Chemical compound with banana odor From Wikipedia, the free encyclopedia

Isoamyl acetate

Isoamyl acetate, also known as isopentyl acetate, is an ester formed from isoamyl alcohol and acetic acid, with the molecular formula C7H14O2. It is a colorless liquid that is only slightly soluble in water, but very soluble in most organic solvents. Isoamyl acetate has a strong odor which is described as similar to both banana and pear.[3] Pure isoamyl acetate, or mixtures of isoamyl acetate, amyl acetate, and other flavors in ethanol may be referred to as banana oil[4] or pear oil.[5]

Quick Facts Names, Identifiers ...
Isoamyl acetate
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Isoamyl acetate
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Names
Preferred IUPAC name
3-Methylbutyl acetate
Systematic IUPAC name
3-Methylbutyl ethanoate
Other names
Isopentyl acetate
Isopentyl ethanoate
Isoamyl acetate
Banana oil
Pear essence
Identifiers
3D model (JSmol)
1744750
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.240
EC Number
  • 204-662-3
101452
KEGG
RTECS number
  • NS9800000
UNII
UN number 1104 1993
  • InChI=1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3 Y
    Key: MLFHJEHSLIIPHL-UHFFFAOYSA-N Y
  • InChI=1/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3
    Key: MLFHJEHSLIIPHL-UHFFFAOYAI
  • O=C(OCCC(C)C)C
Properties
C7H14O2
Molar mass 130.187 g·mol−1
Appearance Colorless liquid
Odor Banana-like[1]
Density 0.876 g/cm3
Melting point −78 °C (−108 °F; 195 K)
Boiling point 142 °C (288 °F; 415 K)
0.3% (20 °C)[1]
Vapor pressure 4 mmHg or 0.533 kPa (20 °C)[1]
−89.4·10−6 cm3/mol
1.4020 at 20°
Hazards
GHS labelling:
GHS02: Flammable
Danger
H226, H315, H319, H335, H336, H372
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P314, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
ThumbHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
3
0
Flash point 25 °C (77 °F; 298 K)
Explosive limits 1.0% (100 °C) – 7.5%[1]
Lethal dose or concentration (LD, LC):
7422 mg/kg (rabbit, oral)
16,600 mg/kg (rat, oral)[2]
6470 ppm (cat)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 100 ppm (525 mg/m3)[1]
REL (Recommended)
TWA 100 ppm (525 mg/m3)[1]
IDLH (Immediate danger)
1000 ppm[1]
Related compounds
Related compounds
Isoamyl formate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Natural occurrence

Isoamyl acetate occurs naturally in many plants, including apple, banana, coffee, grape, guava, lychee, papaya, peach, pomegranate, and tomato.[6][7] It is also released by fermentation processes, including those used for making beer, sake, cognac, and whisky.[6]

Isoamyl acetate is released by a honey bee's sting apparatus where it serves as a pheromone beacon to attract other bees and provoke them to sting.[8]

Production

Isoamyl acetate is prepared by the acid-catalyzed reaction (Fischer esterification) between isoamyl alcohol and glacial acetic acid as shown in the reaction equation below. Typically, sulfuric acid is used as the catalyst. Alternatively, p-toluenesulfonic acid or an acidic ion exchange resin can be used as the catalyst.

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It is also produced synthetically by the rectification of amyl acetate.[9]

Applications

Isoamyl acetate is used to confer banana or pear flavor in foods such as circus peanuts, Juicy Fruit and pear drops.[10] Banana oil and pear oil commonly refer to a solution of isoamyl acetate in ethanol that is used as an artificial flavor.

It is also used as a solvent for some varnishes, oil paints, and nitrocellulose lacquers. As a solvent and carrier for materials such as nitrocellulose, it was extensively used in the aircraft industry for stiffening and wind-proofing fabric flying surfaces, where it and its derivatives were generally known as 'aircraft dope'. Now that most aircraft wings are made of metal, such use is mostly limited to historically accurate reproductions and scale models.

Because of its intense, pleasant odor and its low toxicity, isoamyl acetate is used to test the effectiveness of respirators or gas masks.[11]

References

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