Methyl vinyl ether homopolymer

Product Information

Molecular Formula:
(C3H6O)n
Description
Tacky resin. Water-insoluble above 28º. Used to prepare heat-sensitive latex.50% Aq. Soln.
Synonyms
methyl vinyl ether polymer; Poly(methyl vinyl ether); Poly(vinyl methyl ether); vinyl methyl ether polymer; Ethene, methoxy-, homopolymer; methoxy-ethenhomopolymer; poly(vinylmethylether)
Canonical SMILES
COC=C
InChI
InChI=1S/C3H6O/c1-3-4-2/h3H,1H2,2H3
InChI Key
XJRBAMWJDBPFIM-UHFFFAOYSA-N
Boiling Point
5.5°C at 760mmHg
Melting Point
-188 °F
Flash Point
-69 °F
Density
1.03 g/mL at 25 °C
Solubility
In water, 0.97 wt% /15,000 mg/L/ at 20 °C
Appearance
Colorless, compressed gas or colorless liquid
Application
Used to make polymers or modify polymers for coatings, lacquers, and resins.
Storage
Store at room temperature;Do not permit to freeze
Concentration
50% aqueous solution
Refractive Index
n20/D 1.467
Tg
−31 °C
Vapor Pressure
1316.0 [mmHg]
Henry's Law Constant
3.9X10-3 atm-cu m/mole at 25 °C (est)
Decomposition
When heated to decomposition it emits acrid smoke and irritating fumes.
Odor
Sweet, pleasant

Safety Information

Hazards
Irritant
Handling
Gloves & chemical goggles

Computed Properties

XLogP3
0.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
58.041864811 g/mol
Monoisotopic Mass
58.041864811 g/mol
Topological Polar Surface Area
9.2Ų
Heavy Atom Count
4
Formal Charge
0
Complexity
17.2
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-9158226-B1 Image forming apparatus, electrostatic charge image developing carrier set, and process cartridge set 2014-09-02
EP-2808354-A1 Fast drying, hard elastic, scratch-proof and resistant coating compositions 2014-08-08
WO-2015075280-A1 Polyurethane urea solutions for hair-styling compositions 2014-08-05
US-2015378282-A1 Transfer member and image forming apparatus 2014-06-30
US-2015375176-A1 Membrane filter 2014-06-27
US-2015376505-A1 Polymerizable compound having triple bond, liquid crystal composition and liquid crystal display device 2014-06-27
US-2015375521-A1 Electrostatic printing of cyclodextrin compositions 2014-06-26
US-2015378274-A1 Toner 2014-06-26
US-2015378275-A1 Method for producing toner particles 2014-06-26
WO-2015197662-A1 Copolymer containing oxazoline monomers and use thereof as a cross-linking agent 2014-06-26

Literatures

PMID Publication Date Title Journal
22959184 2012-12-01 Multi-arm histidine copolymer for controlled release of insulin from poly(lactide-co-glycolide) microsphere Biomaterials
22865398 2012-11-15 Electronic fluxes during Diels-Alder reactions involving 1,2-benzoquinones: mechanistic insights from the analysis of electron localization function and catastrophe theory Journal of computational chemistry
23036055 2012-10-23 Dual stimuli-responsive polymeric hollow nanogels designed as carriers for intracellular triggered drug release Langmuir : the ACS journal of surfaces and colloids
22988941 2012-10-17 Acid-triggered release via dePEGylation of fusogenic liposomes mediated by heterobifunctional phenyl-substituted vinyl ethers with tunable pH-sensitivity Bioconjugate chemistry
22721724 2012-10-01 Self-assembly nanomicelles based on cationic mPEG-PLA-b-Polyarginine(R15) triblock copolymer for siRNA delivery Biomaterials
22921144 2012-09-18 Enhancement of surface graft density of MPEG on alginate/chitosan hydrogel microcapsules for protein repellency Langmuir : the ACS journal of surfaces and colloids
22669101 2012-09-15 Influence of skin model on in vitro performance of drug-loaded soluble microneedle arrays International journal of pharmaceutics
22770552 2012-09-04 Synthesis of novel biodegradable methoxy poly(ethylene glycol)-zein micelles for effective delivery of curcumin Molecular pharmaceutics
21926145 2012-09-01 Supramolecular self-assembly of monoend-functionalized methoxy poly(ethylene glycol) and α-cyclodextrin: from micelles to hydrogel Journal of biomaterials applications
22853003 2012-08-22 Thiol-ene click chemistry: computational and kinetic analysis of the influence of alkene functionality Journal of the American Chemical Society
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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