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Key Documents

186325

Sigma-Aldrich

Methyl acetate

ReagentPlus®, 99%

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About This Item

Formula condensata:
CH3COOCH3
Numero CAS:
Peso molecolare:
74.08
Beilstein:
1736662
Numero CE:
Numero MDL:
Codice UNSPSC:
12352108
ID PubChem:
NACRES:
NA.21

Densità del vapore

2.55 (vs air)

Livello qualitativo

Tensione di vapore

165 mmHg ( 20 °C)

Nome Commerciale

ReagentPlus®

Saggio

99%

Forma fisica

liquid

Temp. autoaccensione

936 °F

Limite di esplosione

16 %

Indice di rifrazione

n20/D 1.361 (lit.)

P. eboll.

57-58 °C (lit.)

Punto di fusione

−98 °C (lit.)

Densità

0.934 g/mL at 25 °C

Stringa SMILE

COC(C)=O

InChI

1S/C3H6O2/c1-3(4)5-2/h1-2H3
KXKVLQRXCPHEJC-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Its IR spectra in the vapor phase and in solution form (in CS2 and CCl4) have been reported. It can be synthesized from dimethyl ether via carbonylation in the presence of halide-free catalysts based on zeolites. It has also been reported to be formed during the synthesis of poly(vinyl) alcohol (PVA). It undergoes transesterification reaction with n-octanol in the presence of Amberlyst 15 catalyst to afford octyl acetate and methanol.
Methyl acetate is an aliphatic ester that can be prepared via carbonylation of dimethyl ether over zeolites. MA is formed as a by-product during the preparation of polyvinyl alcohol from acetic acid and methanol.

Applicazioni

Methyl acetate may be used for the preparation of fatty acid methyl esters and triacetin from rapeseed oil via non-catalytic trans-esterification reaction under super-critical conditions.
Methyl acetate may be used in the following:
  • As acyl acceptor in the preparation of biodiesel.
  • Synthesis of ethanol.
  • Preparation of n-butyl acetate, via transesterification reaction with n-butanol in the presence of acidic catalysts.
It may also be used as a precursor in the synthesis of the following:
  • acetic anhydride
  • methyl acrylate
  • vinyl acetate
  • ethyl amide

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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)

8.6 °F - closed cup

Punto d’infiammabilità (°C)

-13 °C - closed cup


Certificati d'analisi (COA)

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Sigma-Aldrich

138185

Hydroxyacetone

Etilacetato ACS reagent, ≥99.5%

Sigma-Aldrich

319902

Etilacetato

Kinetics of transesterification of methyl acetate and n-octanol catalyzed by cation exchange resins.
Liu Y, et al.
Korean Journal of Chemical Engineering, 30(5), 1039-1042 (2013)
Catalysts, Kinetics, and Reactive Distillation for Methyl Acetate Synthesis.
Zuo C, et al.
Industrial & Engineering Chemistry Research, 53(26), 10540-10548 (2014)
A new process for catalyst-free production of biodiesel using supercritical methyl acetate.
Saka S and Isayama Y.
Fuel: The Science and Technology of Fuel and Energy, 88(7), 1307-1313 (2009)
Selective carbonylation of dimethyl ether to methyl acetate catalyzed by acidic zeolites.
Patricia Cheung et al.
Angewandte Chemie (International ed. in English), 45(10), 1617-1620 (2006-01-31)
Synthesis of ethanol from methanol and syngas through an indirect route containing methanol dehydrogenation, DME carbonylation, and methyl acetate hydrogenolysis.
Liu Y, et al.
Fuel Processing Technology, 110, 206-213 (2013)

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