Polyvinyl acetate

Product Information

Molecular Formula:
(C4H6O2)n
Description
Polyvinyl acetate is used as an emulsifier in drug manufacturing.
Synonyms
Poly(vinyl acetate); PVA
IUPAC Name
ethenyl acetate
Canonical SMILES
CC(=O)OC=C
InChI
InChI=1S/C4H6O2/c1-3-6-4(2)5/h3H,1H2,2H3
InChI Key
XTXRWKRVRITETP-UHFFFAOYSA-N
Boiling Point
162 to 163 °F at 760 mmHg
Melting Point
-136 °F
Flash Point
18 °F
Density
1.18 g/cm3
Appearance
Pellets
Application
Used in the production of polyvinyl acetate emulsions, acrylic fiber, and polyvinyl alcohol; Occupational exposure occurs in production workers, painters, and floor layers.
Storage
Store at room temperature
Refractive Index
n20/D 1.462
Tg
32°
LogP
log Kow = 0.73
Vapor Pressure
83 to 140 mmHg at 68 to 86 °F
Henry's Law Constant
5.11X10-4 atm-cu m/mol at 25 °C (est)
Decomposition
WHEN HEATED TO DECOMP, BURNS & EMITS FUMES WITH AN ACRID ODOR.
Odor
An initially pleasant odor which quickly becomes sharp and irritating ... Not unpleasant , sweetish smell in small quantities

Safety Information

Hazards
Harmless-use normal precautions
Handling
Exercise normal care

Computed Properties

XLogP3
0.7
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
86.036779430 g/mol
Monoisotopic Mass
86.036779430 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
65.9
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
US-2016031796-A1 Antimuscarinic compound having a low content of impurities 2014-07-30
US-2015197493-A1 Azepane derivatives and methods of treating hepatitis b infections 2014-01-16
US-2015197533-A1 Azepane derivatives and methods of treating hepatitis b infections 2014-01-16
US-2015225355-A1 Azepane derivatives and methods of treating hepatitis b infections 2014-01-16
US-2016000812-A1 Azepane derivatives and methods of treating hepatitis b infections 2014-01-16
US-9169212-B2 Azepane derivatives and methods of treating hepatitis B infections 2014-01-16
US-9181288-B2 Azepane derivatives and methods of treating hepatitis B infections 2014-01-16
US-9339510-B2 Azepane derivatives and methods of treating hepatitis B infections 2014-01-16
US-2016263256-A1 Process For The Preparation Of Hyperpolarized Carboxylate Compounds 2013-10-28
US-2016200691-A1 Process for the large scale production of 1h-[1,2,3]triazole and its intermediate 1-benzyl-1h-[1,2,3]triazole 2013-09-13

Literatures

PMID Publication Date Title Journal
27794450 2017-02-01 3D engineered In vitro hepatospheroids for studying drug toxicity and metabolism Toxicology in vitro : an international journal published in association with BIBRA
24038327 2013-12-01 Nonlinear responses for chromosome and gene level effects induced by vinyl acetate monomer and its metabolite, acetaldehyde in TK6 cells Environmental and molecular mutagenesis
22698950 2013-01-01 Kinetic aspects of ultrasound-accelerated lipase catalyzed acetylation and optimal synthesis of 4'-acetoxyresveratrol Ultrasonics sonochemistry
22733705 2012-12-01 Modeling of drug release from biodegradable triple-layered microparticles Journal of biomedical materials research. Part A
23124473 2012-11-02 Sol-gel entrapped Candida antarctica lipase B--a biocatalyst with excellent stability for kinetic resolution of secondary alcohols Molecules (Basel, Switzerland)
22989650 2012-11-01 Effect of poly(vinyl acetate-acrylamide) microspheres properties and steric hindrance on the immobilization of Candida rugosa lipase Bioresource technology
22660769 2012-10-01 Insight into microwave irradiation and enzyme catalysis in enantioselective resolution of DL-(±)-3-phenyllactic acid Applied microbiology and biotechnology
22847187 2012-10-01 Immobilization of Pseudomonas fluorescens lipase onto magnetic nanoparticles for resolution of 2-octanol Applied biochemistry and biotechnology
22728393 2012-09-15 Highly efficient biosynthesis of sucrose-6-acetate with cross-linked aggregates of Lipozyme TL 100 L Journal of biotechnology
22349988 2012-09-01 Lipase catalyzed acetylation of 3,5,4'-trihydroxystilbene: optimization and kinetics study Bioprocess and biosystems engineering
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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