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33-0390

Sigma-Aldrich

Vinyl acetate

CP

Synonym(s):

Acetoxyethylene

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About This Item

Linear Formula:
CH3CO2CH=CH2
CAS Number:
108-05-4
Molecular Weight:
86.09
Beilstein:
1209327
MDL number:
MFCD00008713
UNSPSC Code:
12352108
PubChem Substance ID:
329754443

grade

CP

vapor density

3 (vs air)

vapor pressure

88 mmHg ( 20 °C)

form

liquid

autoignition temp.

801 °F

expl. lim.

13.4 %

availability

available only in Japan

refractive index

n20/D 1.395 (lit.)

bp

72-73 °C (lit.)

mp

−93 °C (lit.)

density

0.934 g/mL at 25 °C (lit.)

SMILES string

CC(=O)OC=C

InChI

1S/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H3

InChI key

XTXRWKRVRITETP-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

H225,H332,H335,H351,H412

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Carc. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

17.6 °F

Flash Point(C)

-8 °C

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K Wlodarski et al.
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To improve solubility of tadalafil (Td), a poorly soluble drug substance (3μg/ml) belonging to the II class of the Biopharmaceutical Classification System, its six different solid dispersions (1:1, w/w) in the following polymers: HPMC, MC, PVP, PVP-VA, Kollicoat IR and
Francesca Reineri et al.
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Matthew S Bogdanffy et al.
Toxicology letters, 140-141, 83-98 (2003-04-05)
Understanding the mode of action of carcinogens is critical to scientifically assessing exposure-related risk. Regulatory hazard classification schemes and dose-response assessment paradigms generally require basic knowledge of genotoxic potential to guide decisions on which scheme or paradigm is most appropriate.
S Copelli et al.
Journal of hazardous materials, 192(1), 8-17 (2011-06-03)
Fast and exothermic discontinuous emulsion polymerization processes are particularly difficult to optimize from both safety and productivity point of view because of the occurrence of side undesired reactions (e.g. chain transfer to monomer, backbiting, propagation of tertiary radicals, termination by
Akifumi Nakamura et al.
Journal of the American Chemical Society, 134(30), 12366-12369 (2012-07-25)
Utilization of palladium catalysts bearing a P-chiral phosphine-sulfonate ligand enabled asymmetric copolymerization of vinyl acetate with carbon monoxide. The obtained γ-polyketones have head-to-tail and isotactic polymer structures. The origin of the regio- and stereoregularities was elucidated by stoichiometric reactions of
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