296996
Methyl acetate
anhydrous, 99.5%
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3COOCH3
CAS 번호:
Molecular Weight:
74.08
UNSPSC Code:
12352108
NACRES:
NA.21
PubChem Substance ID:
EC Number:
201-185-2
Beilstein/REAXYS Number:
1736662
MDL number:
Assay:
99.5%
Grade:
anhydrous
Bp:
57-58 °C (lit.)
Vapor pressure:
165 mmHg ( 20 °C)
InChI key
KXKVLQRXCPHEJC-UHFFFAOYSA-N
InChI
1S/C3H6O2/c1-3(4)5-2/h1-2H3
SMILES string
COC(C)=O
grade
anhydrous
vapor density
2.55 (vs air)
vapor pressure
165 mmHg ( 20 °C)
assay
99.5%
form
liquid
autoignition temp.
936 °F
expl. lim.
16 %
impurities
<0.003% water, <0.005% water (100 mL pkg)
evapn. residue
<0.0003%
refractive index
n20/D 1.361 (lit.)
bp
57-58 °C (lit.)
mp
−98 °C (lit.)
density
0.934 g/mL at 25 °C
Quality Level
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General description
Methyl acetate (MA) 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.
Application
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.
Other Notes
The article number 296996-6X1L will be discontinued. Please order the single bottle 296996-1L which is physically identical with the same exact specifications.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
8.6 °F - closed cup
flash_point_c
-13 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Reaction kinetics and chemical equilibrium of homogeneously and heterogeneously catalyzed acetic acid esterification with methanol and methyl acetate hydrolysis
Popken T, et al.
Industrial & Engineering Chemistry Research, 39(7), 2601-2611 (2000)
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)
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