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4S8486

Supelco

Vinyl acetate

analytical standard

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
EC Number:
203-545-4
MDL number:
MFCD00008713
UNSPSC Code:
77101502
PubChem Substance ID:
329757555
NACRES:
NA.24

grade

analytical standard

Agency

EPA 8240,8260

vapor density

3 (vs air)

vapor pressure

88 mmHg ( 20 °C)

description

Separate Source

CofA

current certificate can be downloaded

autoignition temp.

801 °F

feature

standard type calibration

expl. lim.

13.4 %

packaging

pkg of 1 × 100 mg (4S8486)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

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.)

application(s)

environmental
petroleum

format

neat

storage temp.

2-8°C

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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General description

Vinyl acetate is an important vinyl ester, also known as vinyl acetate monomer. It is mainly used in the production of polymers and copolymers, for coating paints, binders, textile, and paper processing industries.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Vinyl acetate is used in the production of polyvinyl acetates, ethylene vinyl acetates for use in textiles, coating and as a PVC alternative respectively.

Other Notes

Contains 3-20 ppm hydroquinone as an inhibitor

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

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 - closed cup

Flash Point(C)

-8 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAC8997
LRAC4288
LRAC0203
LRAB8190
LRAB6853

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Sigma-Aldrich

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Anna Piperno et al.
The Journal of organic chemistry, 75(9), 2798-2805 (2010-04-17)
A new template of C-4'-truncated phosphonated nucleosides (TPCOANs) has been obtained in good yields according to two different routes which exploit the reactivity of a phosphonated nitrone. The one-step procedure based on the 1,3-dipolar cycloaddition of a phosphonated nitrone with
Roberto M Risi et al.
Organic letters, 14(4), 1180-1182 (2012-02-07)
A highly atom-economical total synthesis of (+)-patulolide C has been accomplished in three steps from the known (2R)-8-nonyn-2-ol in 49% overall yield and 93% de. A Rh(I)-catalyzed asymmetric hydroformylation (AHF)/ intramolecular Wittig olefination cascade was utilized to set the C4-hydroxyl
Hercules V Ferreira et al.
Molecules (Basel, Switzerland), 17(8), 8955-8967 (2012-07-28)
The lipase B from Candida antarctica (Novozym 435®, CALB) efficiently catalyzed the kinetic resolution of some aliphatic secondary alcohols: (±)-4-methylpentan-2-ol, (±)-5-methylhexan-2-ol, (±)-octan-2-ol, (±)-heptan-3-ol and (±)-oct-1-en-3-ol. The lipase showed excellent enantioselectivities in the transesterifications of racemic aliphatic secondary alcohols producing the
B Picquet-Varrault et al.
Environmental science & technology, 44(12), 4615-4621 (2010-05-25)
Vinyl acetate is widely used in industry. It has been classified as a high-production volume (HPV) chemical in the United States. To evaluate its impact on the environment and air quality, its atmospheric reactivity toward the three main tropospheric oxidants
María B Blanco et al.
Environmental science & technology, 46(16), 8817-8825 (2012-07-18)
The products formed from the reactions of OH radicals with vinyl acetate and allyl acetate have been studied in a 1080 L quartz-glass chamber in the presence and absence of NO(x) using in situ FTIR spectroscopy to monitor the reactant
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