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Merck

494518

Sigma-Aldrich

Ethylacetat

biotech. grade, ≥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.01

Qualität

biotech. grade

Dampfdichte

3 (20 °C, vs air)

Dampfdruck

73 mmHg ( 20 °C)

Assay

≥99.8%

Form

liquid

Selbstzündungstemp.

801 °F

Expl.-Gr.

2.2-11.5 %, 38 °F

Verunreinigungen

≤0.0009 meq/g Titr. acid
<0.01% water

Abdampfrückstand

<0.0003%

Brechungsindex

n20/D 1.3720 (lit.)

bp

76.5-77.5 °C (lit.)

mp (Schmelzpunkt)

−84 °C (lit.)

Löslichkeit

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

Dichte

0.902 g/mL at 25 °C (lit.)

λ

H2O reference

UV-Absorption

λ: 254 nm Amax: 1.00
λ: 263 nm Amax: 0.05
λ: 275-400 nm Amax: 0.01

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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Allgemeine Beschreibung

Ethyl acetate (EA), a carboxylate ester, is bio-friendly organic solvent with a 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. Low water content, minimal residue and clean UV spectra are the special characteristics of this biotech grade solvent. It can be utilized for biotechnological processes like protein sequencing, peptide and oligonucleotide synthesis.

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.

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


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

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)
Investigation of ethyl acetate reactive distillation process.
Kenig EY, et al.
Chemical Engineering Science, 56(21), 6185-6193 (2001)
Catalytic Acetylation Amines with Ethyl Acetate.
Camacho-Camacho C, et al.
Main Group Metal Chemistry, 31(1-2), 13-20 (2008)
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
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)

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