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Merck

537438

Sigma-Aldrich

Propylacetat

≥99.5%

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About This Item

Lineare Formel:
CH3COOCH2CH2CH3
CAS-Nummer:
Molekulargewicht:
102.13
Beilstein:
1740764
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352108
eCl@ss:
39022103
PubChem Substanz-ID:
NACRES:
NA.21

Dampfdichte

3.5 (vs air)

Qualitätsniveau

Dampfdruck

25 mmHg ( 20 °C)

Assay

≥99.5%

Form

liquid

Selbstzündungstemp.

842 °F

Expl.-Gr.

1.7 %, 37 °F
8 %

Verunreinigungen

≤0.01% Acetic acid (free acid)
≤0.1% Water

Abdampfrückstand

≤0.01%

Farbe

APHA: ≤15

Brechungsindex

n20/D 1.384 (lit.)

bp

102 °C (lit.)

mp (Schmelzpunkt)

−95 °C (lit.)

Dichte

0.888 g/mL at 25 °C (lit.)

SMILES String

CCCOC(C)=O

InChI

1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3

InChIKey

YKYONYBAUNKHLG-UHFFFAOYSA-N

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Allgemeine Beschreibung

Propyl acetate (n-propyl acetate) is the propyl ester of acetic acid. The absolute rate constant for the reaction of n-propyl acetate with OH radicals has been reported to be (k × 10-9lmole-1s-1) = 2.6 ± 0.5lmole-1s-1. Liquid-liquid equilibrium of the ternary system composed of water, acetic acid and propyl acetate has been investigated at various temperatures (298.15, 313.15 and 363.15K). Experimental values were found to be in close agreement with that of UNIQUAC (UNIversal QUAsiChemical) model. It has been identified as one of the volatile ester produced from Penicillium commune.

Anwendung

Propyl acetate may be employed as a solvent for the evaluation of vapor pressure of the polymeric solution of polystyrene. It may be used in the preparation of geranyl acetate.

Piktogramme

FlameExclamation mark

Signalwort

Danger

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Zielorgane

Central nervous system

Zusätzliche Gefahrenhinweise

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

53.2 °F - closed cup

Flammpunkt (°C)

11.8 °C - closed cup


Analysenzertifikate (COA)

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High polymer solutions. Part 7.-Vapour pressure of polystyrene solutions in acetone, chloroform and propyl acetate.
Bawn CEH and Wajid MA.
Transactions of the Faraday Society, 52, 1658-1664 (1956)
Geranyl acetate synthesis by lipase-catalyzed transesterification in supercritical carbon dioxide.
Geranyl acetate synthesis by lipase-catalyzed transesterification in supercritical carbon dioxide.
Chulalaksananukul W, et al.
Enzyme and Microbial Technology, 15(8), 691-698 (1993)
Rate constants for the reaction of OH radicals with n-propyl acetate, sec-butyl acetate, tetrahydrofuran and peroxyacetyl nitrate.
Winer AM, et al.
Chemical Physics, 51(2), 221-226 (1977)
Liquid-liquid equilibria for the ternary system water+ acetic acid+ propyl acetate.
Xiao X, et al.
Journal of Chemical and Engineering Data, 51(2), 582-583 (2006)
A Sunesson et al.
Applied and environmental microbiology, 61(8), 2911-2918 (1995-08-01)
Five fungal species, Aspergillus versicolor, Penicillium commune, Cladosporium cladosporioides, Paecilomyces variotii, and Phialophora fastigiata, were cultivated on two media, malt extract agar and dichloran glycerol agar. Culture flasks provided with inlet and outlet tubes were used and purified, and humidified

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