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Key Documents

439169

Sigma-Aldrich

Etilacetato

suitable for HPLC, ≥99.8%

Sinonimo/i:

EtOAc

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About This Item

Formula condensata:
CH3COOC2H5
Numero CAS:
Peso molecolare:
88.11
Beilstein:
506104
Numero CE:
Numero MDL:
Codice UNSPSC:
12190000
ID PubChem:
NACRES:
NA.21

Densità del vapore

3 (20 °C, vs air)

Livello qualitativo

Tensione di vapore

73 mmHg ( 20 °C)

Saggio

≥99.8%

Forma fisica

liquid

Temp. autoaccensione

801 °F

Limite di esplosione

2.2-11.5 %, 38 °F

tecniche

GC/MS: suitable
HPLC: suitable

Impurezze

<0.050% water

Residuo dopo evaporazione

<0.0003%

Indice di rifrazione

n20/D 1.3720 (lit.)

P. eboll.

76.5-77.5 °C (lit.)

Punto di fusione

−84 °C (lit.)

Solubilità

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

Densità

0.902 g/mL at 25 °C (lit.)

λ

H2O reference

Assorbanza UV

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

applicazioni

food and beverages

Formato

neat

Stringa SMILE

CCOC(C)=O

InChI

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

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Descrizione generale

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.

Applicazioni

Ethyl acetate may be used in the following studies:
  • As solvent for the isolation of Rose hip (Rosa canina L., Rosaceae) powder, via sonication.
  • As solvent for the abstraction of volatile thiols from wine for their quantitative estimation by gas chromatography/mass spectrometry (GC-MS).
  • 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.

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Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Central nervous system

Rischi supp

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

24.8 °F - closed cup

Punto d’infiammabilità (°C)

-4 °C - closed cup


Certificati d'analisi (COA)

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I clienti hanno visto anche

Maria Nikolantonaki et al.
Analytica chimica acta, 660(1-2), 102-109 (2010-01-28)
As volatile thiols are nucleophiles, they are capable of additional reactions with electrophiles. In enology, this concerns reactions between volatile or non-volatile thiols and oxidized phenolic compounds. Initial studies concerning the reactivity of volatile thiols with polyphenols showed that (+)-catechin
Dynamics and control of an ethyl acetate reactive distillation column.
Vora N and Daoutidis P.
Industrial & Engineering Chemistry Research, 40(3), 833-849 (2001)
Towards a green process for bulk-scale synthesis of ethyl acetate: efficient acceptorless dehydrogenation of ethanol.
Martin Nielsen et al.
Angewandte Chemie (International ed. in English), 51(23), 5711-5713 (2012-04-21)
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)
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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