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Documentos Principais

L092004

Sigma-Aldrich

Acetato de etila

Sinônimo(s):

EtOAc

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About This Item

Fórmula linear:
CH3COOC2H5
Número CAS:
Peso molecular:
88.11
Beilstein:
506104
Número CE:
Número MDL:
Código UNSPSC:
12352108
NACRES:
NA.01

densidade de vapor

3 (20 °C, vs air)

Nível de qualidade

pressão de vapor

73 mmHg ( 20 °C)

Ensaio

100% (GC)

forma

liquid

temperatura de autoignição

801 °F

Lim. expl.

2.2-11.5 %, 38 °F

índice de refração

n20/D 1.3720 (lit.)

pb

76.5-77.5 °C (lit.)

pf

−84 °C (lit.)

solubilidade

water: soluble

densidade

0.902 g/mL at 25 °C (lit.)

formato

neat

cadeia de caracteres SMILES

CCOC(C)=O

InChI

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

chave InChI

XEKOWRVHYACXOJ-UHFFFAOYSA-N

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Descrição geral

In the solid-phase synthesis of oligonucleotides, liquid reagents are used in each step of the synthesis cycle. Overall synthesis performance, and therefore total product yield and purity of the crude oligonucleotide, is highly dependent on the chemical purity of the monomers and the supporting liquid reagents and other solvents like ethylacetate, dichloromethane, and dimethylformadine .Ethyl acetate (EA), a carboxylate ester, is a bio-friendly organic solvent with a wide range of industrial applications. Ethyl acetate can be obtained via an esterification reaction between ethyl alcohol and acetic acid in the presence of sulfuric acid. 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.

Aplicação

Ethyl acetate may be used in the following studies:
  • As a solvent for the isolation of Rose hip (Rosa canina L., Rosaceae) powder, via sonication.
  • As a 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.
  • Acetylaton of primary amines to form amides in the presence of dimethyltin(IV) acetic acid distannoxane.

Pictogramas

FlameExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Central nervous system

Perigos de suplementos

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

24.8 °F - closed cup

Ponto de fulgor (°C)

-4 °C - closed cup


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Acetato de etila EMPROVE® ESSENTIAL, Ph. Eur., BP, NF

SAFC

1.00864

Acetato de etila

Acetato de etila EMPLURA®

Supelco

8.22277

Acetato de etila

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Escherichia coli produces the iron-chelating compound enterobactin to enable growth under iron-limiting conditions. After biosynthesis, enterobactin is released from the cell. However, the enterobactin export system is not fully understood. Previous studies have suggested that the outer membrane channel TolC
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Bacterial cholesterol oxidase is commonly used as an experimental tool to reduce cellular cholesterol content. That the treatment also generates the poorly degradable metabolite 4-cholesten-3-one (cholestenone) has received less attention. Here, we investigated the membrane partitioning of cholestenone using simulations
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The aim of the present experiment was to compare silage prepared from maize having a brown midrib (BMR) mutation with control (CTR) maize to identify their effects on enteric methane emission, digesta mean retention time (MRT), ruminal fermentation and digestibility.

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