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4S8486

Supelco

Vinyl acetate

analytical standard

Synonyme(s) :

Acetoxyethylene

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About This Item

Formule linéaire :
CH3CO2CH=CH2
Numéro CAS:
Poids moléculaire :
86.09
Numéro Beilstein :
1209327
Numéro CE :
Numéro MDL:
Code UNSPSC :
77101502
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Agence

EPA 8240,8260

Densité de vapeur

3 (vs air)

Pression de vapeur

88 mmHg ( 20 °C)

Description

Separate Source

CofA (certificat d'analyse)

current certificate can be downloaded

Température d'inflammation spontanée

801 °F

Caractéristiques

standard type calibration

Limite d'explosivité

13.4 %

Conditionnement

pkg of 1 × 100 mg (4S8486)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.395 (lit.)

Point d'ébullition

72-73 °C (lit.)

Pf

−93 °C (lit.)

Densité

0.934 g/mL at 25 °C (lit.)

Application(s)

environmental
petroleum

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CC(=O)OC=C

InChI

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

Clé InChI

XTXRWKRVRITETP-UHFFFAOYSA-N

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Description générale

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.

Autres remarques

Acétate de vinyle

Produits recommandés

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.

Pictogrammes

FlameHealth hazardExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

17.6 °F - closed cup

Point d'éclair (°C)

-8 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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
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
Francesca Reineri et al.
Nature communications, 6, 5858-5858 (2015-01-06)
The advent of nuclear spins hyperpolarization techniques represents a breakthrough in the field of medical diagnoses by magnetic resonance imaging. Dynamic nuclear polarization (DNP) is the most widely used method, and hyperpolarized metabolites such as [1-(13)C]-pyruvate are shown to report
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.

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