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Sigma-Aldrich

Hexylacetat

99%

Synonym(e):

Caprylacetat

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About This Item

Lineare Formel:
CH3COO(CH2)5CH3
CAS-Nummer:
142-92-7
Molekulargewicht:
144.21
Beilstein:
1747138
EG-Nummer:
205-572-7
MDL-Nummer:
MFCD00009524
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24846804
NACRES:
NA.22

Assay

99%

Brechungsindex

n20/D 1.409 (lit.)

bp

168-170 °C (lit.)

mp (Schmelzpunkt)

−80 °C (lit.)

Dichte

0.87 g/mL at 25 °C (lit.)

SMILES String

CCCCCCOC(C)=O

InChI

1S/C8H16O2/c1-3-4-5-6-7-10-8(2)9/h3-7H2,1-2H3

InChIKey

AOGQPLXWSUTHQB-UHFFFAOYSA-N

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Allgemeine Beschreibung

Hexyl acetate is an ester and is commonly used as a solvent for resins, polymers, fats, and oils. It can also be used as a flavoring agent in the food industry. It is produced by acid catalyzed liquid phase esterification of n-hexanol and acetic acid.

Anwendung

Hexyl acetate was used to study the activity of diamondback moth sex pheromone and larval frass volatiles, as well as green leaf volatiles from cabbage, on the natural enemies of the pest.

Biochem./physiol. Wirkung

Hexyl acetate has antimicrobial activity and can be used to improve the safety of minimally processed fruits. Hexyl acetate is a fruity smelling fluid used as flavoring agent or in perfumes. Hexyl acetate is a green leaf volatile from cabbage Brassica oleracea var. capitata L.

Piktogramme

FlameEnvironment
GHS02,GHS09

Signalwort

Warning

H-Sätze

H226,H411

Gefahreneinstufungen

Aquatic Chronic 2 - Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

132.8 °F - closed cup

Flammpunkt (°C)

56 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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Sigma-Aldrich

29240

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Pentylacetat 99%

Sigma-Aldrich

109584

Pentylacetat

cis-3-Hexenylacetat ≥98%, stabilized, FCC, FG

Sigma-Aldrich

W317101

cis-3-Hexenylacetat

Nonyl acetate ≥97%, FCC

Sigma-Aldrich

W278807

Nonyl acetate

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Supelco

8.18700

n-Amyl acetate

Intensification of enzyme catalysed synthesis of hexyl acetate using sonication
AR Deshmukh, et al.
Green Processing and Synthesis, 6, 55-62 (2017)
Rosalba Lanciotti et al.
Journal of agricultural and food chemistry, 51(10), 2958-2963 (2003-05-02)
The aims of this work were to evaluate the effects of different concentrations of hexanal, (E)-2-hexenal, hexyl acetate, and their mixtures on the fate of pathogenic species such as Escherichia coli, Salmonella enteritidis, and Listeria monocytogenes inoculated in model systems
G V P Reddy et al.
Journal of chemical ecology, 28(1), 131-143 (2002-03-02)
The parasitoids Trichogramma chilonis (Hymenoptera: Trichogrammatidae) and Cotesia plutellae (Hymenoptera: Braconidae), and the predator Chrysoperla carnea (Neuroptera: Chrysopidae), are potential biological control agents for the diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae). We present studies on the interactions between these bioagents
Synthesis of n-hexyl acetate by reactive distillation.
Schmitt M, et al.
Chemical Engineering and Processing, 43(3), 397-409 (2004)
Valentina Canuti et al.
Journal of agricultural and food chemistry, 67(9), 2647-2659 (2019-02-14)
Sangiovese is the most widespread Italian red cultivar and constitutes the basis of internationally known wines such as Chianti and Brunello di Montalcino. Outside of Europe, Argentina is the largest producer, followed by the United States. This study sought to
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