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POLY(VINYL ACETATE) Suppliers list
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
Products Intro: Product Name:POLY(VINYL ACETATE)
Purity:99% Package:25KG;5KG;1KG
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Tel: +86-0371-86658258
Products Intro: Product Name:SEC-BUTYLACETATE
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Company Name: Xiamen AmoyChem Co., Ltd
Tel: +86-592-6051114 +8618959220845
Products Intro: Product Name:Poly(vinyl acetate) 235
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Tel: 86-13657291602
Products Intro: Product Name:POLY(VINYL ACETATE)
Company Name: Shandong chuangyingchemical Co., Ltd.
Tel: 18853181302
Products Intro: Product Name:Poly(vinyl acetate)

POLY(VINYL ACETATE) manufacturers

  • $0.00 / 1KG
  • 2023-01-21
  • CAS:9003-20-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500000kg
  • $12.00 / 20KG
  • 2022-12-23
  • CAS:9003-20-7
  • Min. Order: 20KG
  • Purity: 98%
  • Supply Ability: 1-10mt
  • $150.00 / 20Kg/Drum
  • 2021-11-02
  • CAS:9003-20-7
  • Min. Order: 20KG
  • Purity: 99%
  • Supply Ability: 200000T

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POLY(VINYL ACETATE) Basic information
Product Categories:Polymers;Hydrophobic Polymers;Materials Science;Polymer Science;Vinyl Esters
Mol File:9003-20-7.mol
POLY(VINYL ACETATE) Chemical Properties
Melting point 60°C
Boiling point 70-150 °C
density 1.18 g/mL at 25 °C
refractive index n20/D 1.467
Fp >100℃
storage temp. 2-8°C
solubility ketones, ethers and aromatic hydrocarbons: soluble
form pellets
color Clear
Stability:Stable. Incompatible with strong oxidizing agents, strong bases. Combustible.
IARC3 (Vol. 19, Sup 7) 1987
EPA Substance Registry SystemPolyvinyl acetate (9003-20-7)
Safety Information
Risk Statements 45-46
Safety Statements 24/25
WGK Germany 3
RTECS AK0920000
HS Code 39051900
Hazardous Substances Data9003-20-7(Hazardous Substances Data)
ToxicityLD50 oral in mouse: > 25gm/kg
MSDS Information
ACROS English
SigmaAldrich English
ALFA English
POLY(VINYL ACETATE) Usage And Synthesis
Chemical PropertiesThe degree of polymerization of polyvinyl acetate typically is 100 to 5000. The ester groups of the polyvinyl acetate are sensitive to base hydrolysis and will slowly convert PVAc into polyvinyl alcohol and acetic acid.
Under alkaline conditions, boron compounds such as boric acid or borax cause the polymer to cross-link, forming tackifying precipitates or slime.
Chemical Propertiestransparent pellets or white powder
HistoryPolyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte.
The monomer, vinyl acetate, was first produced on an industrial scale by addition of acetic acid to acetylene with a mercury(I) salt[3] but it is now primarily made by palladium catalyzed oxidative addition of acetic acid to ethylene.
UsesPolyvinyl acetate is used as an adhesive for porous materials such as wood, paper, cloth and in handicrafts. It also finds application as a primer for drywall, as wallpaper adhesive, as the film-forming ingredient in water-based (latex) paints and as an envelope adhesive. It is used as a raw material for the preparation of other polymers like polyvinyl alcohol and polyvinyl acetate phthalate (PVAP). It plays an important role in the lamination of metal foils.
UsesAs an emulsion in water, aPVAc emulsions are used as adhesives for porous materials, particularly for wood, paper, and cloth, and as a consolidant for porous building stone, in particular sandstone . Uses :
As wood glue PVAc is known as "white glue" and the yellow "carpenter's glue" or PVA glue.
As paper adhesive during paper packaging converting
In bookbinding and book arts, due to its flexible strong bond and non-acidic nature (unlike many other polymers). The use of PVAC on the Archimedes Palimpsest during the 20th century greatly hindered the task of disbinding the book and preserving and imaging the pages in the early 21st century, in part because the glue was stronger than the parchment it held together.
The stiff homopolymer PVAc, but mostly the more soft copolymer a combination of vinyl acetate and ethylene, vinyl acetate ethylene (VAE), is used also in paper coatings, paint and other industrial coatings, as binder in nonwovens in glass fibers. sanitary napkins, filter paper and in textile finishing
PVAc can also be used as coating to protect cheese from fungi and humidity.
Polyvinyl acetate is also the raw material to make other polymers like : Polyvinyl alcohol -[HOCHCH2]-: Polyvinyl acetate is partially or completely hydrolysed to give polyvinyl alcohol. This reversible saponification and esterification reaction was a strong hint for Hermann Staudinger in the formulation of his theory of macro molecules.
Polyvinyl acetate phthalate (PVAP): Polyvinyl acetate is partially hydrolyzed and then esterified with phthalic acid.
Usesdrug delivery, hemodynamics, wound dressing, coatings
DefinitionChEBI: A polymer composed of repeating acetoxyethylene units.
Production MethodsPolyvinyl acetate is derived from the polymerization of vinyl acetate; the catalysts used in polymerization may include hydrogen peroxide, peroxy sulfates, or various redox combinations. The polymerization process is described as being carried out by charging all ingredients to the reactor, heating to reflux, and stirring until the reaction is complete. Typically, only a part of the monomer and catalyst is initially charged; the remainder is added during the course of the reaction.
PreparationPVAc is a vinyl polymer. Polyvinyl acetate is prepared by polymerization of vinyl acetate monomer (free radical vinyl polymerization of the monomer vinyl acetate).
General DescriptionPoly(vinyl acetate) [PVAc] is a biocompatible and biodegradable polymer as it has hydrolyzable groups in the side chain,also it is non-toxic and non-carcinogenic.Owing to its biologically friendly nature , it is used in various biomedical application such as artificial organ implant, contact lens,cardiovascular devices and cartilage skin. It is also used in wound dressing and various drug-delivery applications. It has been accepted as reference standard for universal calibration in gel permeation chromatography.
HazardQuestionable carcinogen.
Industrial usesPolyvinyl acetate is a leathery, colorless thermoplasticmaterial that softens at relatively lowtemperatures and that is relatively stable to lightand oxygen. The polymers are clear and noncrystalline.The chief applications of polyvinylacetate are as adhesives and binders for waterbasedor emulsion paints.
Vinyl acetate is conveniently prepared bythe reaction of acetylene with acetic acid.
Safety ProfileVery low toxicity by ingestion. Questionable carcinogen. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS
Purification MethodsPrecipitate it from acetone by addition of n-hexane.
POLY(VINYL ACETATE) Preparation Products And Raw materials
Raw materialsBenzoyl peroxide-->Ammonium persulfate-->Rosin-->Polyethylene-->Vinyl acetate-->Poly(vinyl alcohol)-->Dibutyl phthalate
Preparation Productslatex paint
Tag:POLY(VINYL ACETATE)(9003-20-7) Related Product Information
N/A Ethyl 2-(Chlorosulfonyl)acetate Dimethyl-diphenylpolysiloxane Cyclosilazanes, di-Me,Me hydrogen, polymers with di-Me, Me hydrogen silazanes, reaction products with3-(triethoxysilyl)-1-propanamine DOW CORNING FS CHEMICALLY INERT FLUID Olibanum oil Ethephon POLY(VINYL ACETATE-CO-BUTYL MALEATE-CO-ISOBORNYL ACRYLATE) poly(vinyl chloride)-poly(vinyl acetate) copolymer Poly(vinyl acetate-2-ethylhexyl acrylate) Reaction products of: poly(vinyl acetate), partially hydrolyzed, with (E)-2-(4-formylstyryl)-3,4-dimethylthiazoliummethyl sulfate low VOC polyvinyl acetate emulsion paint PVAC-VAE complex emulsion adhesive Pour point depressant T804 antistatic polyvinylacetate alcohol-soluble resin poly(vinyl acetate-maleic anhydride) Poly(vinyl acetate) dispersion 30 per cent POLY(VINYL ACETATE-CO-CROTONIC ACID)