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Merck

494518

Acétate d′éthyle

biotech. grade, ≥99.8%

Synonyme(s) :

EtOAc

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A propos de cet article

Formule linéaire :
CH3COOC2H5
Numéro CAS:
141-78-6
Poids moléculaire :
88.11
UNSPSC Code:
12352108
NACRES:
NA.01
PubChem Substance ID:
329757457
EC Number:
205-500-4
Beilstein/REAXYS Number:
506104
MDL number:
MFCD00009171
Assay:
≥99.8%
Grade:
biotech. grade
Vapor pressure:
73 mmHg ( 20 °C)

Principaux documents

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InChI key

XEKOWRVHYACXOJ-UHFFFAOYSA-N

InChI

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

SMILES string

CCOC(C)=O

grade

biotech. grade

vapor density

3 (20 °C, vs air)

vapor pressure

73 mmHg ( 20 °C)

assay

≥99.8%

Quality Level

100

autoignition temp.

801 °F

expl. lim.

2.2-11.5 %, 38 °F

impurities

≤0.0009 meq/g Titr. acid, <0.01% water

evapn. residue

<0.0003%

refractive index

n20/D 1.3720 (lit.)

mp

−84 °C (lit.)

solubility

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

density

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

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Catégories apparentées

General description

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.
Our biotech solvents offer exceptional quality for reliable RNA extraction, ensuring optimal laboratory performance. With low water content and minimal residue, give clean UV spectra to minimize contamination.
  • High-Quality Biotech Solvents: Designed for optimal laboratory performance with low water content and minimal residues.
  • Ideal for RNA Extraction: Essential for genetic testing and research applications like PCR.
  • Ensures Integrity of Genetic Material: Promotes reliable and reproducible results.
  • Industry Compliant: Suitable for both academic and commercial laboratories, enhancing research efficiency.

Application

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

EUH066

Classe de stockage

3 - Flammable liquids

wgk

WGK 1

flash_point_f

24.8 °F - closed cup

flash_point_c

-4 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
SHBR6244
SHBP7220
SHBQ0210
SHBP3776
SHBQ1531

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Consulter la Bibliothèque de documents

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)
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)
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
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