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Key Documents

Safety Information

V1503

Sigma-Aldrich

Vinyl acetate

contains 3-20 ppm hydroquinone as inhibitor, ≥99%

Synonym(s):

VAc, Acetoxyethylene

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About This Item

Linear Formula:
CH3CO2CH=CH2
CAS Number:
Molecular Weight:
86.09
Beilstein:
1209327
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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vapor density

3 (vs air)

vapor pressure

88 mmHg ( 20 °C)

Assay

≥99%

autoignition temp.

801 °F

contains

3-20 ppm hydroquinone as inhibitor

expl. lim.

13.4 %

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.)

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1 of 4

This Item
GF50506028GF28127921GF59311717
铁 foil, 25x25mm, thickness 0.5mm, hard, 99.5%

GF29599138

铁 foil, 25x25mm, thickness 0.15mm, hard, 99.5%

GF50506028

铁 foil, 25x25mm, thickness 0.1mm, hard, 99.5%

GF28127921

铁 foil, 25x25mm, thickness 0.25mm, hard, 99.5%

GF59311717

form

foil

form

foil

form

foil

form

foil

manufacturer/tradename

Goodfellow 295-991-38

manufacturer/tradename

Goodfellow 505-060-28

manufacturer/tradename

Goodfellow 281-279-21

manufacturer/tradename

Goodfellow 593-117-17

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

density

7.86 g/mL at 25 °C (lit.)

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

resistivity

9.71 μΩ-cm

mp

1535 °C (lit.)

mp

1535 °C (lit.)

mp

1535 °C (lit.)

mp

1535 °C (lit.)

Application

Vinyl acetate has been used as an acyl donor for enzyme-catalyzed acylation reactions.[1][2]

Signal Word

Danger

Hazard Statements

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 - closed cup

Flash Point(C)

-8 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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    Kinetic resolution of 4-chloro-2-(1-hydroxyalkyl) pyridines using Pseudomonas cepacia lipase.
    Busto E
    Nature Protocols, 1(4), 2061-2061 (2006)
    Nhan Thanh Thien Huynh et al.
    Molecules (Basel, Switzerland), 24(24) (2019-12-22)
    5-Acetoxymethyl-2-furfural (AMF) was prepared from D-fructose via 1,6-diacetylfructose (DAF) through a simple two-step reaction pathway. Immobilized enzyme (Novozym 435) was found to be the best enzymatic catalyst for the trans-esterification step (yielding 94.6% DAF). In the dehydration step, while soluble
    Lipases efficiently stearate and cutinases acetylate the surface of arabinoxylan films.
    Stepan AM
    Journal of Biotechnology, 167(1), 16-23 (2013)
    Tianyou Zeng et al.
    iScience, 23(3), 100904-100904 (2020-02-28)
    Polyethylene (PE) is one of the most widely used materials in the world, but it is virtually undegradable and quickly accumulates in nature, which may contaminate the environment. We utilized the cobalt-mediated radical copolymerization (CMRP) of ethylene and cyclic ketene
    Ping Xu et al.
    Polymers, 11(2) (2019-04-10)
    Hyperbranched polycaprolactone with controlled structure was synthesized by reversible addition-fragmentation chain transfer radical ring-opening polymerization along with self-condensed vinyl polymerization (SCVP) of 2-methylene-1,3-dioxepane (MDO). Vinyl 2-[(ethoxycarbonothioyl) sulfanyl] propanoate (ECTVP) was used as polymerizable chain transfer agent. Living polymerization behavior was

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    RAFT polymerization offers precise control, enabling tailored synthesis of complex polymer structures.

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