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Anhui Liwei Chemical Co., Limited.

Food Contact Reagent Grade VAM (Food Polymer Lab Development)

    • Product Name: Food Contact Reagent Grade VAM (Food Polymer Lab Development)
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
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    Specifications
    HS Code 541690
    Product Name Food Contact Reagent Grade VAM (Food Polymer Lab Development)
    Chemical Name Vinyl Acetate Monomer
    Cas Number 108-05-4
    Molecular Formula C4H6O2
    Molecular Weight 86.09 g/mol
    Grade Food Contact Reagent Grade
    Appearance Clear colorless liquid
    Physical State Liquid
    Odor Sweet, fruity odor
    Purity >=99.9%
    Boiling Point 72.7 °C at 760 mmHg
    Melting Point -93 °C
    Flash Point -8 °C (closed cup)
    Autoignition Temperature 427 °C
    Density 0.934 g/cm³ at 20 °C
    Vapor Pressure 115 hPa at 20 °C
    Refractive Index 1.395 at 20 °C
    Solubility In Water 2.5 g/100 mL at 20 °C
    Water Content <=0.05%
    Acidity As Acetic Acid <=0.005%
    Inhibitor Hydroquinone 15-20 ppm
    Storage Temperature 2-30 °C

    As an accredited Food Contact Reagent Grade VAM (Food Polymer Lab Development) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Food Contact Reagent Grade VAM (Food Polymer Lab Development) supplied in 1 kg sealed containers for laboratory research use.
    Container Loading (20′ FCL) 20′ FCL loaded with food-grade VAM in clean, secure drums, ensuring purity and safe transport for polymer lab development.
    Shipping Ship as UN1301 Vinyl Acetate, inhibited, Class 3, PG II. Pack in approved steel drums or IBCs, ensure inhibitor concentration maintained, protect from heat/ignition sources, ground equipment, and label flammable. This reagent-grade material is for laboratory development only, not for use in finished food-contact articles.
    Storage Store Food Contact Reagent Grade VAM in a tightly sealed, corrosion-resistant container under inert gas, in a cool, dry, well-ventilated area. Keep away from heat, sparks, open flames, sunlight, oxidizers, and peroxides. Ensure polymerization inhibitor remains active, monitor storage temperature, and use grounded equipment to prevent static discharge.
    Shelf Life Shelf life: 6 months when stored sealed, under inert gas, away from light and heat, in original container.
    Application of Food Contact Reagent Grade VAM (Food Polymer Lab Development)

    When high-integrity heat sealing of flexible food-contact packaging is required, reagent-grade vinyl acetate monomer (VAM) is copolymerised with ethylene under high pressure. Feedstock quality for food polymer lab development is specified as VAM purity ≥99.9% by gas chromatography, water content ≤100 mg/kg by Karl Fischer titration, and hydroquinone monomethyl ether inhibitor at 3–5 ppm before monomer purification. Feedstock purification prior to reactor charging includes removal of the inhibitor by vacuum distillation at 30–35 °C at 20–25 kPa, reducing inhibitor content below 1 ppm; water is controlled because water terminates organometallic catalysts and shifts the crystallinity profile of the resulting ethylene-vinyl acetate (EVA) copolymer. Compliance evidence for finished food-contact EVA is established under 21 CFR 177.1340 and under EU Regulation (EU) No 10/2011, where vinyl acetate monomer is assigned a specific migration limit of 12 mg/kg in food simulants; residual vinyl acetate in the extruded pellet is routinely verified below 0.5 mg/kg by headspace gas chromatography–mass spectrometry. The formulation window for sealant layers uses vinyl acetate content of 5–18 wt% in the copolymer for standard lamination sealants and 18–28 wt% for high-cling over-wrap films. Vinyl acetate content below 5 wt% raises seal initiation temperature above 120 °C, while content above 28 wt% lowers Vicat softening temperature and increases blocking during roll storage. Melt flow rate is measured under ISO 1133-1:2022 at 190 °C/2.16 kg, typically 2–8 g/10 min for cast film and 0.5–3 g/10 min for blown film. Downstream conversion on pilot and production lines uses a coextrusion setup with a barrier or polyolefin core, an adhesive tie layer, and an EVA sealant skin; the EVA skin is processed through a single-screw extruder with L/D 24:1–30:1 and barrel temperature profile 170–230 °C, while the cast film unit runs at chill-roll temperature 15–25 °C to prevent roll blocking. Terminal finished product types include retortable pouch lidding films, frozen food lamination webs, fresh-cut produce bags, and tamper-evident medical food-pack seals where peelable fusion is specified.

    Vinyl acetate content (wt%)Seal initiation range (°C)Thermal seal test methodTypical downstream format
    5–9105–120ASTM F2029 with ASTM D3418 melting referenceLidding films for polypropylene trays
    9–1885–105ASTM F2029Frozen food lamination sealants
    18–2870–85ASTM F2029Stretch-cling over-wrap and case-ready film

    What Role Does VAM-Derived VAE Dispersion Play in Food-Contact Paperboard Coating?

    Polymerised in semicontinuous emulsion reactors at total solids 55–60 wt%, vinyl acetate–ethylene (VAE) dispersions derived from food-contact reagent-grade VAM are adjusted with sodium hydroxide or ammonia to pH 4.5–5.5 and blended with calcium carbonate or kaolin clay slurries for paperboard coating. For food-contact board, the binder addition ratio is 10–25 dry wt% of the total dry coating solids, with pigment volume concentration maintained at 45–60%; higher binder fractions reduce bending stiffness and increase blocking of stacked food cartons. Compliance for the coated paperboard is asserted under 21 CFR 176.170 for aqueous and fatty food categories and 21 CFR 176.180 for dry food categories; China GB 9685-2016 positive-list verification is applied for coating additives in export grades. Finished prints or coatings are evaluated for migration using ASTM D4754 or EU EN 1186 migration protocols. In downstream application, the coating color is applied on an off-machine or in-line blade coater at line speeds of 150–400 m/min, using coat weights of 8–18 g/m² per side; drying is performed with infrared and air-float dryers at web temperatures of 120–150 °C, followed by soft-nip calendering at 80–120 kN/m to reduce surface roughness. Operator-level failure modes include rod streaks and binder migration when viscosity exceeds 1200 mPa·s at 25 °C, and pH drift below 4.0 can induce dispersion destabilisation when calcium ion hardness in process water exceeds 300 ppm. Formulation incompatibilities include borax and high-zinc oxide additives, which raise ionic strength and can produce irreversible gritting. Terminal finished product types for this VAE route include hot and cold paper cups, folded carton stock for frozen and dry foods, barrier priming layers under extrusion-coated LDPE, and food-contact paperboard plates.

    Conversion of Reagent-Grade VAM to PVOH for Water-Soluble Food Contact Testing

    Controlled alcoholysis of VAM-derived polyvinyl acetate yields polyvinyl alcohol (PVOH) with degree of hydrolysis selected at 86.5–89.0 mol% for cold-water dissolution at 20 °C and 98.0–99.0 mol% for hot-water-insensitive barrier films. Compliance for PVOH film in food contact is based on 21 CFR 177.1670, and the residual vinyl acetate monomer migrating from PVOH must remain below the EU (EU) No 10/2011 SML of 12 mg/kg; methanol process residue is typically controlled below 50 mg/kg in the dried polymer, measured by headspace gas chromatography with flame ionisation detection. For water-soluble food-contact films, the aqueous casting formulation contains 4–8 wt% PVOH solids, with glycerol or sorbitol plasticiser added at 5–15 phr relative to dry PVOH and sodium acetate buffer from saponification reduced by methanol washing to ≤1 wt%. Downstream production from reagent-grade VAM proceeds through solution polymerisation in methanol at 60–65 °C using azo or peroxide initiators, followed by continuous saponification with sodium methylate at 30–40 °C; the resulting PVOH is dissolved in deionised water at 85–95 °C and cast on a polyethylene terephthalate carrier at drying temperatures of 85–110 °C. Processing at ambient relative humidity above 60% requires pre-drying of the PVOH resin to moisture below 0.5 wt% to avoid bubble defects in cast film. Published data for this specific reagent-grade VAM-to-PVOH migration configuration under repeated-use testing is limited; each formulation must be validated under 21 CFR 177.1670 extraction and end-use simulant conditions before commercial release. Terminal finished product types are pre-portioned food-additive pouches that dissolve during industrial mixing, water-soluble release films for food-contact mould liners, and cold-water-soluble bags for pre-weighed bakery improvers.

    If Oxygen Transmission Below 1 cm³/(m²·day·atm) Is Required, the EVOH Route from VAM Governs Barrier Consistency

    To achieve oxygen transmission rate below 1 cm³/(m²·day·atm) at 23 °C/0% RH in rigid or flexible food packaging, the VAM-derived ethylene-vinyl alcohol (EVOH) copolymer is manufactured from an EVA precursor with vinyl acetate content of 56–73 mol%, then saponified to a degree of hydrolysis ≥99.5 mol%. The final EVOH resin contains ethylene at 27–44 mol%, and the residual vinyl acetate monomer content is controlled below 0.5 mg/kg to meet 21 CFR 177.1350 and the EU (EU) No 10/2011 SML of 12 mg/kg for vinyl acetate. In coextrusion, EVOH is processed between polyolefin tie layers on a three- or five-layer cast line; the EVOH extruder barrel profile is held at 210–230 °C, with a processing window of only ±5 °C before gel formation reduces barrier consistency. Field-scale extrusion has shown that idle periods longer than 15 minutes require purging with LDPE at 220 °C, because EVOH degrades rapidly above 250 °C and forms crosslinked black specks in the film. Downstream terminal product types include PP/EVOH/PP barrier cups, retortable stand-up pouches, modified atmosphere packaging trays, and aseptic bag-in-box films where oxygen ingress below 0.5 cm³/(m²·day·atm) is specified. Oxygen transmission testing is performed according to ASTM D3985 at 23 °C/50% RH, while vinyl acetate monomer migration is verified by EN 1186 total immersion with aqueous and fatty simulants.

    Polyvinyl acetate synthesised from food-contact reagent-grade VAM is incorporated into chewing gum base as a masticatory resin at 20–45 wt% of the gum base, with weight-average molecular weight ranges of 12,000–50,000 Da selected according to chew texture, flavour release, and plasticiser retention. Compliance for this application is determined under 21 CFR 172.615, where polyvinyl acetate is permitted with a minimum molecular weight of 2,000 Da; JECFA specifications and the EU food additive framework may also apply when PVAc is declared as a food additive or gum base component. The residual vinyl acetate monomer in the PVAc resin must be reduced below 1 mg/kg by steam stripping or vacuum devolatilisation, and peroxide initiator decomposition products are removed by filtration or thermal treatment. Downstream processing occurs in heated sigma-blade mixers at 115–120 °C, where PVAc is melt-blended with food-grade ester resins, microcrystalline wax, calcium carbonate, and elastomers until torque stabilises; the homogeneous gum base is cooled on a chill belt, pelletised, and later extruded into chewing gum sticks or pellets. Terminal finished product types include sugar-coated chewing gum pellets, stick gum, and dragee centres. Published compositional data for specific proprietary gum bases is limited; qualification of PVAc from reagent-grade VAM requires batch-specific analysis of residual monomer, heavy metals, and overall migration to match the food-contact declaration.

    Vinyl Chloride–Vinyl Acetate Copolymer Coatings for Rigid Metal Substrates

    Vinyl chloride–vinyl acetate copolymer resins, prepared with VAM at 3–15 wt% in the monomer feed, are dissolved in methyl ethyl ketone/toluene blends to 20–35 wt% solids for reverse-roll application onto tinplate and chromium-coated steel. Compliance for this can-coating class is defined by 21 CFR 175.300, which lists resinous and polymeric coatings for metal food-contact surfaces, and by EU (EC) No 1935/2004 with supporting migration testing under EN 1186; vinyl acetate monomer migration must not exceed 12 mg/kg when tested with food simulants assigned under (EU) No 10/2011. Formulation additions include stabilizers such as epoxidised soybean oil at 2–5 phr, phenolic or melamine crosslinkers at 3–10 phr, and phosphoric acid catalyst at 0.1–0.5 wt% of total solids to promote adhesion to steel. In downstream coil coating, the lacquer is applied by reverse-roll coater at dry film weights of 5–12 g/m² and cured in high-velocity hot-air ovens at 190–205 °C for 10–12 minutes, producing a continuous film with crosshatch adhesion classification 5B under ASTM D3359. Terminal finished product types include drawn food cans, drawn-and-ironed can bodies, easy-open lids, and food jar closures. Formulation limits include incompatibility with zinc oxide or amine-based adhesion promoters, which can catalyse dehydrochlorination and reduce coating flexibility.

    Application sectorPrimary regulationCritical VAM-derived specificationKey test method
    EVA sealant webs21 CFR 177.1340, (EU) No 10/2011residual VAM 0.5 mg/kg maxASTM F2029, ISO 1133-1:2022
    VAE paperboard coating21 CFR 176.170binder addition 10–25 dry wt%EN 1186, ASTM D4754
    PVOH water-soluble film21 CFR 177.1670hydrolysis 86.5–89.0 mol%EN 1186
    EVOH barrier21 CFR 177.1350saponification ≥99.5 mol%ASTM D3985
    PVAc gum base21 CFR 172.615Mw 12,000–50,000 DaJECFA residual monomer
    Can coatings21 CFR 175.300VAM in copolymer 3–15 wt%ASTM D3359, EN 1186
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    Certification & Compliance
    More Introduction

    Food Contact Reagent Grade VAM (Food Polymer Lab Development), model VAM-FC-RG-LD, is a vinyl acetate monomer, CAS 108-05-4, refined for laboratory-scale and pilot-scale synthesis of polymers intended for food-contact applications. The material is supplied as a clear, mobile liquid with a molar mass of 86.09 g/mol, a density of 0.934 g/cm³ at 20 °C, a normal boiling point of 72.7 °C, a closed-cup flash point of -8 °C, and a vapor pressure of 11.8 kPa at 20 °C. The product carries a controlled inhibitor concentration of 3–5 ppm 4-methoxyphenol, selected to provide storage stability while minimizing interference with radical polymerization initiation. Unlike bulk VAM distributed for general polymer and adhesive manufacture, this reagent-grade lot is released under a low-trace-impurity profile for food-contact polymer development, including polyvinyl acetate dispersions, ethylene-vinyl acetate copolymers, vinyl acetate-vinyl versatate copolymers, and polyvinyl alcohol after alcoholysis.

    The designation “reagent grade” in this context does not imply direct food additive use. It defines a vinyl acetate monomer stream that is controlled for trace carbonyls, chloride, acidity, water, nonvolatile residue, and inhibitor consistency beyond conventional commodity VAM. These controls are relevant because monomer impurities can survive polymerization, contribute to organoleptic defects, alter reaction kinetics, and appear in migration testing of the finished polymer.

    What renders a VAM lot acceptable for food-contact polymer bench work?

    Compliance with ASTM D2190 alone does not capture the trace aldehydes and chloride that can influence polymer color, odor, or migration performance. The food-contact reagent grade is therefore specified for assay, water, acidity, color, nonvolatile residue, inhibitor concentration, and total aldehydes as acetaldehyde. Water functions as a chain-transfer and hydrolysis participant in VAM polymerizations, so the upper water limit is set at 0.05 wt%. Acidity as acetic acid is held to 0.005 wt% because free acid accelerates hydrolysis of acetate groups and contributes to corrosion in glass-lined equipment. Color is limited to 5 Pt-Co units. Total aldehydes as acetaldehyde are limited to 25 ppm because acetaldehyde and related carbonyls produce off-odors in water-based emulsions and can react with amine-bearing stabilizers. The MEHQ concentration is held within 3–5 ppm rather than a broader commercial range to reduce induction-period variability during seeded emulsion protocols. Table 1 lists the control parameters and corresponding analytical methods.

    ParameterMethodLimit
    Vinyl acetate assayASTM D2190 capillary GC-FID≥99.9%
    Water contentASTM E203 Karl Fischer coulometric≤0.05 wt%
    Acidity as acetic acidASTM D1613≤0.005 wt%
    ColorASTM D1209≤5 Pt-Co
    MEHQ inhibitorHPLC-UV at 280 nm3–5 ppm
    Total aldehydes as acetaldehydeInternal DNPH derivatization HPLC≤25 ppm
    Nonvolatile residueASTM D1353≤0.001 wt%
    ChlorideIon chromatography≤1 ppm

    Each production batch is released only when the analytical set falls within these control limits. Because this reagent grade is intended for polymer synthesis rather than direct food contact, regulatory compliance is assessed on the resulting polymer matrix under the applicable food-contact regulation. This distinction is critical: a monomer specification cannot substitute for migration testing of the finished article.

    In emulsion polymerization of vinyl acetate for food-contact polyvinyl acetate dispersions, the reactor is first purged with nitrogen until residual oxygen is below 100 ppm in the headspace. The aqueous phase is prepared with deionized water and a food-contact-approved polyvinyl alcohol stabilizer in the 2–6 wt% range based on total monomer. The monomer phase is charged at 40–60 °C, and initiator, typically potassium persulfate or ammonium persulfate, is fed as an aqueous solution. Because the MEHQ inhibitor in this product is maintained at 3–5 ppm, the induction period before the exotherm begins is typically 15–30 min in a 1 L jacketed glass reactor with anchor stirring at 200 min-1. Higher inhibitor variance widens the induction period across replicate runs, so lot-to-lot consistency is a primary difference from commodity VAM. After monomer feed completion, the temperature is held at 70–80 °C for 60–90 min to reduce free monomer, followed by redox finishing with tertiary butyl hydroperoxide and sodium formaldehyde sulfoxylate if residual VAM is targeted below 0.1 wt%. Residual vinyl acetate in the isolated dispersion is quantified by headspace gas chromatography with flame ionization detection; the limit of quantitation is 5 mg/kg in the dispersion.

    When scaling from suppressed-inhibitor synthesis to 50 L pilot trials

    Transfer from glass reactors to a 50 L jacketed stainless steel reactor with a 2:1 height-to-diameter ratio changes heat removal capacity and initiator dosing sensitivity. In the larger vessel, the same MEHQ-controlled feed may require the initial initiator shot to be split into two portions separated by 10 min, because the lower surface-to-volume ratio delays the exotherm and can allow unreacted initiator to accumulate. At reaction temperatures above 75 °C, vinyl acetate homopolymerization undergoes chain transfer to polymer, leading to long-chain branching and a broadened molecular weight distribution. Gel fraction can become measurable above 80 °C in unstabilized bulk polymerization. The product’s low water content is particularly relevant in high-pressure ethylene-vinyl acetate copolymerization, where water and acetic acid influence catalyst productivity and polymer acid number. For EVA trials in a continuous stirred autoclave reactor, the VAM feed is typically deoxygenated and injected at 40–70 MPa with ethylene; the reactor temperature is held between 150–250 °C depending on target vinyl acetate incorporation. Published data for film-grade EVA made specifically from this reagent-grade VAM configuration is limited; however, the impurity profile is designed to remain below thresholds known to cause film haze and off-taste.

    Differences from commodity and low-inhibitor product streams

    Commodity VAM shipped for emulsion adhesives and paint binders is frequently controlled only for assay, water, acidity, color, and inhibitor. Such lots may contain total aldehydes above 50 ppm and trace chloride above 5 ppm, which can compromise sensory performance and reactor long-term stability. Low-inhibitor VAM grades, in contrast, may be supplied with MEHQ below 2 ppm to minimize induction time, but those lots require refrigerated storage below 10 °C and have a reduced shelf life because of peroxide accumulation during transit. The food-contact reagent grade avoids both extremes by holding MEHQ at 3–5 ppm, a range that is storage-stable and does not require inhibitor removal before polymerization. The grade also excludes inhibitor packages based on high-level hydroquinone, which can require caustic washing during polymer workup to prevent color formation. Chloride control is another differentiator: VAM streams with chloride above 1 ppm accelerate pitting in 316L stainless steel reactors and can interfere with cationic initiators used for vinyl acetate-vinyl versatate copolymerization. For food-contact polymer development, the selection criterion is therefore not monomer assay alone but the trace-impurity panel affecting migration, odor, color, and polymerization kinetics.

    Total aldehyde content is not a classical food-contact migration parameter but functions as a quality marker because acetaldehyde forms adducts with active hydrogen atoms in stabilizers and can produce organoleptic defects in film and lid materials. In polyvinyl alcohol production, residual aldehyde in the monomer can survive hydrolysis and appear as carbonyl content in the polyvinyl alcohol, affecting aqueous solution color and viscosity stability. The total aldehydes limit of 25 ppm in this reagent grade is lower than typical commodity VAM, which may carry 50–100 ppm total carbonyls. Chloride is limited to 1 ppm because ionic chloride promotes corrosion in 316L stainless steel reactors and can destabilize emulsion formulations containing divalent cations.

    Food-contact compliance is demonstrated on the finished polymer, not on the monomer

    Under EU Regulation 10/2011, vinyl acetate is permitted as a monomer in food-contact plastics with a specific migration limit of 12 mg/kg. The overall migration limit for the finished article is 10 mg/dm². In the United States, vinyl acetate polymers are covered by multiple clearances: ethylene-vinyl acetate copolymers intended for food contact are addressed in 21 CFR 177.1350, polyvinyl alcohol in 21 CFR 177.1670, and vinyl acetate-containing coatings may fall under 21 CFR 175.300 or 175.105 depending on end use. China GB 4806.6 and GB 9685 may also apply to resins and additives, but the required migration testing must be performed on the specific polymer formulation. The product does not carry a food-contact clearance for direct use; it is a polymerization feedstock.

    Regulation/StandardScopeRelevant parameter or limit
    EU 10/2011Food-contact plasticsSpecific migration limit for vinyl acetate 12 mg/kg
    FDA 21 CFR 177.1350Ethylene-vinyl acetate copolymersVinyl acetate content restrictions and extraction testing
    FDA 21 CFR 177.1670Polyvinyl alcoholResidual vinyl acetate specification and migration testing
    ASTM D2190Vinyl acetate monomer specificationAssay, water, acidity, color, inhibitor, distillation range
    GB 4806.6Food-contact plastic resinsOverall migration and specific migration testing

    Storage and handling constraints are set by the product’s vapor pressure and flammability, not by polymer performance. The monomer should be kept in nitrogen-blanketed, epoxy-phenolic lined drums at 15–25 °C; under these conditions, shelf life is 12 months from the date of manufacture. Contact with exposed copper or brass should be avoided because copper ions can promote oxidative polymerization. Strong acids and amines should also be avoided because they accelerate ester hydrolysis. Transfer lines should be grounded and fitted with flame arrestors. Before beginning laboratory polymerization, the monomer should be sampled for inhibitor concentration after every transfer, because MEHQ can be depleted by oxygen exposure and by prolonged contact with unblanketed headspace.