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650528

Sigma-Aldrich

Acétate d'éthyle

HPLC Plus, for HPLC, GC, and residue analysis, 99.9%

Synonyme(s) :

EtOAc

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About This Item

Formule linéaire :
CH3COOC2H5
Numéro CAS:
Poids moléculaire :
88.11
Numéro Beilstein :
506104
Numéro CE :
Numéro MDL:
Code UNSPSC :
12190000
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

HPLC Plus
for residue analysis

Agence

suitable for EPA ACB B21-02
suitable for EPA ACB B23-05b

Densité de vapeur

3 (20 °C, vs air)

Pression de vapeur

73 mmHg ( 20 °C)

Pureté

99.9%

Forme

liquid

Température d'inflammation spontanée

801 °F

Limite d'explosivité

2.2-11.5 %, 38 °F

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

≤0.03% water
≤1.0 ppb Fluorescence (quinine) at 365 nm
≤10 ng/L Pesticide residue analysis (as heptachlor epoxide)

Résidus d'évap.

≤0.0001%

Indice de réfraction

n20/D 1.3720 (lit.)

Point d'ébullition

76.5-77.5 °C (lit.)

Pf

−84 °C (lit.)

Solubilité

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

Densité

0.902 g/mL at 25 °C (lit.)

λ

H2O reference

Absorption UV

λ: 256 nm Amax: ≤1.00
λ: 275 nm Amax: ≤0.05
λ: 300 nm Amax: ≤0.03
λ: 325-400 nm Amax: ≤0.005

Format

neat

Chaîne SMILES 

CCOC(C)=O

InChI

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

Clé InChI

XEKOWRVHYACXOJ-UHFFFAOYSA-N

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Description générale

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 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. EA is an effective alternate solvent of diethyl ether, employed for the concentration of eggs, larvae, and cysts in fecal specimens during the Formalin-ether sedimentation technique. Acetaldehyde is reaction intermediate formed during the oxidative combustion of ethanol and ethyl acetate in the presence of copper oxide embedded on Ce-doped titania surface.

Application

Suitable for HPLC, spectrophotometry, environmental testing

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Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Organes cibles

Central nervous system

Risques supp

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

24.8 °F - closed cup

Point d'éclair (°C)

-4 °C - closed cup


Certificats d'analyse (COA)

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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)
Perspectives for the biotechnological production of ethyl acetate by yeasts.
Loser C, et al.
Applied Microbiology and Biotechnology, 98(12), 5397-5415 (2014)
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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