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Merck

537446

Sigma-Aldrich

Ethylacetat

ReagentPlus®, ≥99.8%

Synonym(e):

EtOAc

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About This Item

Lineare Formel:
CH3COOC2H5
CAS-Nummer:
Molekulargewicht:
88.11
Beilstein:
506104
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352108
PubChem Substanz-ID:
NACRES:
NA.21

Dampfdichte

3 (20 °C, vs air)

Qualitätsniveau

Dampfdruck

73 mmHg ( 20 °C)

Produktlinie

ReagentPlus®

Assay

≥99.8%

Form

liquid

Selbstzündungstemp.

801 °F

Expl.-Gr.

2.2-11.5 %, 38 °F

Verunreinigungen

≤0.003 mg/mL non-volatile matter
≤0.02% Ethyl alcohol
≤0.05% water

Brechungsindex

n20/D 1.3720 (lit.)

bp

76.5-77.5 °C (lit.)

mp (Schmelzpunkt)

−84 °C (lit.)

Löslichkeit

alcohol: soluble(lit.)
chloroform: soluble(lit.)
water: soluble

Dichte

0.902 g/mL at 25 °C (lit.)

Format

neat

SMILES String

CCOC(C)=O

InChI

1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3

InChIKey

XEKOWRVHYACXOJ-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Ethyl acetate, a carboxylate ester, is bio-friendly organic solvent with wide range of industrial applications. Its synthesis by reactive distillation and by acceptorless dehydrogenative dimerization of ethanol has been explored. Its utility as a less toxic alternative to diethyl ether in the formalin-ether (F-E) sedimentation procedure for intestinal parasites has been investigated. Its ability as an acyl acceptor in the immobilized lipase-mediated preparation of biodiesel from crude vegetable oils has been examined. The complete degradation of ethyl acetate to CO2 using manganese octahedral molecular sieve (OMS-2) has been investigated.

Anwendung

Ethyl acetate may be used in the following processes:
  • Preparation of thin films of TiO2 (titanium dioxide) on glass.
  • As an extraction medium in the multi-residue analysis of pesticide residues in fruit and vegetables.
  • Acetylation of primary amines to form amides in the presence of dimethyltin(IV) acetic acid distannoxane.
Meets urethane grade requirements (H2O ≤ 0.05%)

Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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)

24.8 °F - closed cup

Flammpunkt (°C)

-4 °C - closed cup

Persönliche Schutzausrüstung

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


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1 of 2

Dynamics and control of an ethyl acetate reactive distillation column.
Vora N and Daoutidis P.
Industrial & Engineering Chemistry Research, 40(3), 833-849 (2001)
Christer Jansson et al.
Journal of chromatography. A, 1023(1), 93-104 (2004-02-06)
A new multi-residue method for determination of pesticide residues in a wide variety of fruit and vegetables, using the National Food Administration (NFA) ethyl acetate extraction and determination by means of LC-MS/MS, is presented. The method includes pesticides normally detected
Perspectives for the biotechnological production of ethyl acetate by yeasts.
Loser C, et al.
Applied Microbiology and Biotechnology, 98(12), 5397-5415 (2014)
Anatase thin films on glass from the chemical vapor deposition of titanium (IV) chloride and ethyl acetate.
O'Neill SA, et al.
Chemistry of Materials, 15(1), 46-50 (2003)
Manganese oxide OMS-2 as an effective catalyst for total oxidation of ethyl acetate.
Gandhe AR, et al.
Applied Catalysis. B, Environmental, 72(1), 129-135 (2007)

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