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27227-M

Sigma-Aldrich

Etilacetato

puriss., meets analytical specification of Ph. Eur., BP, NF, ≥99.5% (GC)

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:
12352108
ID PubChem:
NACRES:
NA.21

Densità del vapore

3 (20 °C, vs air)

Livello qualitativo

Tensione di vapore

73 mmHg ( 20 °C)

Grado

puriss.

Saggio

≥99.5% (GC)

Forma fisica

liquid

Temp. autoaccensione

801 °F

Qualità

meets analytical specification of Ph. Eur., BP, NF

Limite di esplosione

2.2-11.5 %, 38 °F

Impurezze

residual solvents, complies
≤0.005% free acid (as CH3COOH)
≤0.01% methyl. comp.(as acetic acid methylester)
≤0.1% ethanol (GC)
≤0.10% water (Karl Fischer)
≤0.2% related subst. (GC)

Residuo dopo evaporazione

≤0.003%

Indice di rifrazione

n20/D 1.371-1.373
n20/D 1.3720 (lit.)

P. eboll.

76.5-77.5 °C (lit.)

Punto di fusione

−84 °C (lit.)

Densità

0.898-0.902 g/mL at 20 °C
0.894-0.898 g/mL at 25 °C
0.902 g/mL at 25 °C (lit.)

Compatibilità

complies for appearance of solution
complies for reaction against H2SO4
corresponds for chromatography
passes test for identity (IR)

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, a carboxylate ester, is a bio-friendly organic solvent with a wide range of industrial applications such as specialized or sensitive chemical synthesis & catalysis; reaction monitoring, metal-sensitive reactions, and highly sensitive purifications.

Applicazioni


  • [Determination of 12 prohibited veterinary drug residues in pig urine by ultra high performance liquid chromatography-tandem mass spectrometry]: Ethyl acetate is utilized for sample preparation in this advanced method to detect drug residues in animal samples, emphasizing its role in veterinary pharmaceutical compliance (Wan et al., 2024).

  • Therapeutic effect of Ginkgetin on smoke-induced airway inflammation by down-regulating the c/EBPβ signaling pathway and CCL2 expression: This study explores the anti-inflammatory properties of Ginkgetin, where ethyl acetate is used in the extraction process, highlighting its utility in biomedical research (Tao et al., 2024).

  • Effect of methanol extract of Plectranthus esculentus N.E.Br tuber and its fractions on indices of benign prostatic hyperplasia in Wistar rats: Ethyl acetate is employed in the extraction of bioactive compounds for pharmacological studies, showing its critical role in therapeutic applications (Kanu et al., 2024).

  • Phytochemical evaluation of Ziziphus mucronata and Xysmalobium undulutum towards the discovery and development of anti-malarial drugs: Demonstrates the use of ethyl acetate in phytochemical screenings, contributing to the development of new anti-malarial medications (Buthelezi et al., 2024).

  • The First Records of the In Silico Antiviral and Antibacterial Actions of Molecules Detected in Extracts of Algerian Fir (Abies numidica De Lannoy) Using LC-MS/MS Analysis: This research utilizes ethyl acetate for extracting compounds from plants for antiviral and antibacterial testing, underscoring its importance in the study of natural products (Benouchenne et al., 2024).

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)

26.6 °F - closed cup

Punto d’infiammabilità (°C)

-3.00 °C - closed cup


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K H Young et al.
Journal of clinical microbiology, 10(6), 852-853 (1979-12-01)
Ethyl acetate appears to be a satisfactory subsitute solvent for diethyl ether in the Formalin-ether sedimentation technique. In comparative studies, concentration of organisms with ethyl acetate was equal to or greater than that with diethyl ether. No distortion or alteration

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