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Pentaerythritol Triacrylate

    • Product Name: Pentaerythritol Triacrylate
    • Factroy Site: Wusu, Tacheng Prefecture, Xinjiang, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Bouling Chemical Co., Limited
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    Specifications
    HS Code 856605
    Product Name Pentaerythritol Triacrylate
    Cas Number 3524-68-3
    Molecular Formula C14H18O7
    Molecular Weight G Per Mol 298.29
    Appearance colorless to pale yellow clear liquid
    Density At 25c G Per Ml 1.18
    Refractive Index N20 D 1.483
    Viscosity At 25c Mpa S 600-800
    Functionality 3
    Hydroxyl Value Mg Koh Per G 188
    Acid Value Mg Koh Per G <=1.0
    Water Content Percent <=0.5
    Inhibitor MEHQ 100-300 ppm
    Flash Point >110 °C
    Solubility soluble in common organic solvents; insoluble in water
    Polymerization Type free-radical

    As an accredited Pentaerythritol Triacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Pentaerythritol Triacrylate is supplied in 1 L amber glass bottles with chemical-resistant caps, sealed closures, and hazard-compliant labeling for safe storage.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Pentaerythritol Triacrylate palletized in drums, loaded and secured in a 20′ FCL for safe chemical transport.
    Shipping Ship Pentaerythritol Triacrylate as a stabilized industrial monomer in compatible, tightly closed, labeled containers. Protect from heat, light, moisture, and contamination to prevent polymerization; avoid spills and environmental release. Follow the SDS, carrier requirements, and applicable dangerous-goods classifications.
    Storage Store Pentaerythritol Triacrylate in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, flames, and oxidizing agents. Keep containers tightly closed, preferably under dry air or inert gas, and maintain the polymerization inhibitor. Avoid UV/visible light, initiators, and incompatible acids or bases. Observe shelf life and inspect containers regularly.
    Shelf Life Typically 12 months when stored in sealed containers in a cool, dry, dark place with inhibitor present.
    Application of Pentaerythritol Triacrylate

    Within high-gloss UV-cured topcoat systems for prefinished wood flooring and rigid PVC plank wear layers, pentaerythritol triacrylate is introduced at 10–25 wt% of the total coating formulation to increase crosslink density without reducing application viscosity to the level associated with monomeric diacrylates. The residual primary hydroxyl group differentiates PETA from trimethylolpropane triacrylate by increasing hydrogen-bonding capacity at the coating-substrate interface, which is relevant to wetting on oak veneer, ceramic-filled engineered wood, and plasticized PVC films. Compliance for toy-contact furniture and floor coverings is referenced to EN 71-3:2019+A1:2021 extractable element limits and ASTM F963-17, while industrial coating performance is evaluated against ISO 15184:2020 pencil hardness, ASTM D3359-17 crosshatch adhesion, and ASTM D523 specular gloss. The downstream production sequence uses a two-roller coater followed by medium-pressure mercury lamps rated at 120 W/cm; line speeds between 10 m/min and 25 m/min are monitored for film cure by solvent resistance testing under ASTM D5402. Terminal product types include abrasion-classified engineered wood flooring and rigid luxury vinyl tile wear layers. The operational boundary is defined by the embrittlement threshold: above 25 wt% PETA, the cured film loses elongation rapidly and shows increased microcracking under caster-chair loading, while shelf stability in open reservoirs beyond 8 hours may be compromised if primary amine synergists are present because the acrylate groups undergo ambient aza-Michael addition.

    Why Does Microgravure Coating of Overprint Varnishes Demand a Working Viscosity Below 500 mPa·s?

    Roll-fed packaging overprint varnish lines use pentaerythritol triacrylate at 10–20 wt% of the varnish formulation to depress high-shear viscosity in urethane acrylate oligomer bases and to maintain consistent transfer from anilox cells to biaxially oriented polypropylene and polyethylene terephthalate films. The relevant regulatory framework for food packaging outer coatings is Regulation (EC) No 1935/2004, supported by migration testing under EN 1186 where a direct-contact varnish is qualified; in the United States, compliance is assessed under 21 CFR 175.300 when the varnish is part of the food-contact coating system, and printers align with the Swiss Ordinance SR 817.023.21 for packaging inks and varnishes. The production line is a flexo or gravure microgravure station with a 120–250 L/cm anilox specification and a closed-chamber doctor blade system, running at 120–200 m/min. After application, the film passes under medium-pressure mercury or doped gallium lamps configured for 100–200 mJ/cm² UVA to avoid distortion on heat-sensitive substrates. Terminal product types include food carton overprint varnishes, label protective lacquers, and blister-pack lidding films. The ratio window is limited by oxygen inhibition at low film weight: below 10 wt% PETA, surface conversion falls and rub resistance on printed cartons drops under ISO 1518-1 scratch testing; above 20 wt%, the cured film becomes hard but increasingly curl-prone on 12 µm PET, requiring adjustment of the elastomer roller pressure and web tension.

    Milled UV flexographic ink concentrates for high-speed label and shrink-sleeve printing on corona-treated polyolefin films incorporate pentaerythritol triacrylate as both a reactive diluent and a pigment-wetting monomer through the residual hydroxyl group. The pigment dispersion stage is performed on a bead mill with a chamber volume of 0.5–5 L, zirconium oxide beads of 0.3–0.8 mm diameter, and grinding temperatures held below 45 °C to prevent auto-polymerization of the acrylate groups. Addition ratios in the let-down ink are between 5 wt% and 12 wt%, with higher loadings reserved for high-strength black linework where low film weight must maintain optical density. Compliance is linked to the EuPIA Exclusion Policy for printing inks, REACH EC 1907/2006 restrictions for acrylates, and the Swiss Ordinance SR 817.023.21 for printed food-contact materials where applicable. Production printing uses photopolymer plate sleeves with a Shore A durometer of 65–75, chambered anilox rolls at 800–1,200 L/cm, and press speeds up to 180 m/min. Terminal product types are pressure-sensitive labels for beverage bottles, shrink sleeves for dairy cups, and in-mold labels for rigid packaging. A process limitation is the tendency of PETA to raise ink tack above 12 wt%; at that point, plate picking and ink misting increase on high-speed CI flexo presses unless let-down is adjusted with a monofunctional diluent and the photopolymer plate surface is re-conditioned.

    Stereolithography Resin Networks and Inhibitor Partitioning

    Vat photopolymerization formulations for 405 nm digital light processing and 355 nm stereolithography use pentaerythritol triacrylate at 20–45 wt% as the dominant multifunctional crosslinker in urethane acrylate or epoxy methacrylate matrices. The high acrylate functionality reduces the gelation dose but increases volumetric shrinkage, so the resin is processed in closed vats with controlled temperature at 25–30 °C and continuous recirculation to maintain homogeneous inhibitor distribution. Compliance for medical simulation models is assessed under ISO 10993-5:2009 cytotoxicity; for consumer and educational parts, EN 71-3:2019+A1:2021 migration limits are often required by distributors. Production equipment uses an LED engine at 405 nm with layer exposure between 1.0 s and 3.5 s per 50 µm layer, followed by two-stage washing in isopropyl alcohol or propylene glycol monomethyl ether acetate and post-curing under 405 nm LED lamps at 30–60 mW/cm² for 20–60 min. Terminal product types include orthodontic models, investment casting patterns, hearing aid shell try-ins, and drill guides for dental surgery. The deep-dive process conflict is the oxygen-inhibited surface layer: at layer thicknesses below 25 µm, the top surface retains uncured acrylate groups that are only fully consumed during post-cure. Resins exceeding 45 wt% PETA produce stiff but brittle parts; measured tensile elongation under ASTM D638-14 falls below the ductile threshold needed for snap-fit assembly prototypes, and flexural modulus under ISO 178:2019 rises steeply.

    When PETA Replaces TMPTA in Optical Fiber Primary Buffer Formulations

    Optical fiber primary buffer resins are formulated with pentaerythritol triacrylate at 5–12 wt% in the inner primary layer and at 8–20 wt% in the harder secondary coating to balance low-temperature hydrogen evolution and microbending resistance. The replacement of trimethylolpropane triacrylate by PETA introduces a residual hydroxyl group that alters the hydrogen-bonding network; this becomes critical in draw towers where coating is applied wet-on-wet immediately after melt draw at line speeds from 1,200 m/min to 2,000 m/min. Compliance is benchmarked to Telcordia GR-20-CORE generic reliability requirements and IEC 60793-2-50:2018 for single-mode optical fibre specifications, with additional measurement of fiber curl and attenuation under temperature-humidity cycling. The production process uses pressurized dual coating dies and two UV lamp arrays per coating layer, each array delivering an integrated dose of 200–400 mJ/cm² at the fiber surface. Terminal product types are bend-insensitive single-mode fibers for FTTH drop cable and high-bandwidth multimode fibers for data center interconnects. The operational boundary is water absorption: because the residual hydroxyl group increases hydrophilic character relative to TMPTA, primary coatings with PETA above 12 wt% require more rigorous dehydration of the draw tower gas supply and can show higher attenuation increase in 85 °C / 85% RH damp-heat testing unless the outer secondary coating remains intact. Published data for this specific configuration is limited, so each fiber coating formulation is qualified on the production draw tower rather than extrapolated from resin bench tests.

    Electronic Conformal Coating Resins Under Humid Condensation Exposure

    Conformal coating formulations for printed circuit board assemblies incorporate pentaerythritol triacrylate at 10–25 wt% of the UV-curable resin fraction to obtain fast surface cure on selective coating cells and to maintain edge coverage on component leads. Qualification under IPC-CC-830B includes moisture and insulation resistance testing at 85 °C / 85% RH with 50 V DC bias, and flame retardance is commonly reported as UL 94 V-0 at 25–50 µm dry film thickness, with additional compliance to RoHS Directive 2011/65/EU. The production process is a selective spray system with closed-loop viscosity control, applying the material at 40–60 °C through a reciprocating head, followed by UV cure using 365 nm high-pressure mercury lamps and a secondary thermal cure at 80–110 °C for 15–30 min to convert shadow zones under ball grid arrays. Terminal product types include automotive engine control modules, white goods inverter boards, and industrial sensor housings. A significant processing conflict is compatibility with no-clean flux residues: PETA-rich coatings can extract residual amine activators from flux deposits, causing darkening and localized undercure at component standoff gaps; therefore, assembly lines specify flux low in amine activators or add a pre-coat plasma cleaning step. Above 25 wt% PETA, the cured coating exhibits higher dielectric constant drift under humid condensation, evaluated by ASTM D149-20 dielectric breakdown and ASTM D257-14 surface resistivity measurements.

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    Certification & Compliance
    More Introduction

    Commercial quantities of pentaerythritol triacrylate (PETA, CAS 3524-68-3; C14H18O7, molecular weight 298.29 g/mol) are supplied as clear, medium-viscosity trifunctional acrylate monomers with one residual primary hydroxyl group per molecule. Industrial designations include Sartomer SR444, Allnex PETIA, Miramer M340, and Double Bond Chemical PET3A. The typical commercial assay is not a single discrete triester; chromatographic profiles commonly show pentaerythritol triacrylate as the dominant component with minor pentaerythritol tetraacrylate and diacrylate species. This distribution directly affects viscosity, cure response, and dermal sensitization potential. Published technical data sheets place the viscosity of standard grades between 600 and 1200 mPa·s at 25°C when measured by rotational viscometry in accordance with ASTM D2196 or ISO 3219. Density is normally 1.18–1.20 g/cm³ at 20°C. The theoretical hydroxyl number is approximately 188 mg KOH/g; commercial values are typically 180–200 mg KOH/g depending on tetraacrylate and diacrylate content. The compound is used as a reactive diluent and crosslinker in ultraviolet- and electron-beam-cured formulations where elevated crosslink density, surface hardness, and solvent resistance are required.

    What Distinguishes Pentaerythritol Triacrylate from Other Multifunctional Acrylates?

    The principal structural difference between PETA and trimethylolpropane triacrylate (TMPTA, CAS 15625-89-5, molecular weight 296.32 g/mol) is the residual hydroxyl group in PETA. TMPTA is a hydrocarbon-core triacrylate with no pendant hydroxyl; its viscosity is typically 70–150 mPa·s at 25°C. PETA sits at the higher end for trifunctional acrylates because intermolecular hydrogen bonding increases internal friction. Compared with difunctional reactive diluents such as 1,6-hexanediol diacrylate (HDDA, viscosity 5–15 mPa·s), PETA provides substantially higher crosslink density and faster through-cure but at the cost of higher volumetric shrinkage and greater irritation potential. Trimethylolpropane trimethacrylate (TMPTMA) is a methacrylate analogue with lower free-radical propagation rate and typical viscosity of 30–60 mPa·s; it reduces surface oxygen inhibition but delivers slower final conversion in acrylate-dominated systems. In UV-cure screen inks and overprint varnishes, PETA raises pencil hardness and methyl ethyl ketone double rub resistance relative to HDDA at equivalent mass addition, while reducing flexibility and increasing brittleness.

    PropertyPentaerythritol triacrylateTMPTATMPTMAHDDA
    Nominal functionality3 acrylate plus 1 hydroxyl3 acrylate3 methacrylate2 acrylate
    Viscosity at 25°C600–1200 mPa·s70–150 mPa·s30–60 mPa·s5–15 mPa·s
    Residual hydroxylprimary, nominal 188 mg KOH/gnonenonenone
    Relative crosslink densityhighhighmoderatelower
    Volatilitylowlowlowhigher
    Skin sensitization potentialhighhighmoderatemoderate

    Specification Profile and Batch Acceptance Criteria

    Batch release documentation for PETA typically includes appearance, color, viscosity, density, refractive index, acid value, moisture, inhibitor content, and flash point. Actual certificates of analysis vary by manufacturer and grade; the table below represents common commercial release windows, not a universal specification.

    ParameterTypical commercial release rangeTest method
    AppearanceClear liquid, free of suspended matterVisual
    Color, APHA≤ 100ASTM D1209
    Viscosity600–1200 mPa·s at 25°CASTM D2196 / ISO 3219
    Density1.18–1.20 g/cm³ at 20°CASTM D1475
    Refractive index1.480–1.485 at 25°CASTM D1218
    Acid value≤ 2.0 mg KOH/gASTM D974
    Moisture≤ 0.20 wt%ASTM E203
    MEHQ inhibitor200–500 ppmHPLC
    Flash point, closed cup> 100°CASTM D93
    Hydroxyl number180–200 mg KOH/gASTM E222

    In roller-applied UV wood coatings, PETA is blended with urethane acrylate or epoxy acrylate oligomers and a small fraction of difunctional diluent. Coating lines using differential-speed rollers and medium-pressure mercury arc lamps typically adjust lamp output to deliver full surface cure without exceeding the heat deflection limits of thin veneer or medium-density fiberboard. Adhesion is evaluated by cross-hatch tape pull per ASTM D3359, and solvent resistance is measured by methyl ethyl ketone double rubs per ASTM D4752. The residual hydroxyl group improves wetting on polar wood substrates and can support post-cure adhesion under high humidity, but high PETA loading increases internal stress and can reduce adhesion on oily tropical hardwoods if surface preparation is inadequate. Published numerical loading ranges for specific commercial formulations are limited because final recipes are proprietary; however, independent coating studies consistently show that replacing a difunctional aliphatic acrylate with PETA raises hardness and chemical resistance while lowering flexibility unless a urethane acrylate oligomer is present.

    When Hydroxyl Retention Alters Formulation Design

    The residual hydroxyl group is not an inert bystander. In dual-cure urethane acrylate systems, PETA can participate in isocyanate crosslinking after UV exposure if free isocyanate remains. This property enables moisture-cure post-crosslinking but also creates a shelf-life risk if PETA is blended with isocyanate-functional oligomers at ambient temperature. The hydroxyl content also raises moisture affinity; formulations stored in open vessels with relative humidity above 60% absorb water and drift in viscosity and acid value. For polyurethane acrylate oligomers, the hydroxyl residue can reduce oligomer compatibility and require higher ketone or aromatic solvent content in solventborne UV inks. In radical-cure systems, the hydroxyl group is largely nonreactive but increases viscosity temperature sensitivity. Heated doctor chambers or heated supply reservoirs are used in gravure printing to maintain transfer consistency because the viscosity rise in PETA-containing inks is more pronounced than for TMPTA-based inks. Incompatibility with amine-based additives must be considered: amine synergists can accelerate Michael addition with acrylate double bonds during storage, leading to viscosity increase and premature gelation. Pre-drying with molecular sieves is required for moisture-sensitive applications such as optical fiber coatings and photopolymer printing plates.

    Stereolithography and jet-printed photopolymer resins use PETA as a reactive diluent for high-modulus, high-heat-deflection builds. Resin compounding houses adjust viscosity to 300–1000 mPa·s at 25°C for layer thicknesses of 50–100 µm; tensile specimens are tested per ASTM D638-14 and flexural properties per ASTM D790-17. PETA raises modulus and lowers elongation at break relative to difunctional polyethylene glycol diacrylate, but also increases water uptake because of the residual hydroxyl. In printed circuit board solder mask inks, PETA contributes to alkali developability when blended with acid-functional acrylate resins, with development confirmed in aqueous sodium carbonate solution at 0.8–1.0 wt% and 30–40°C. In electronics applications, the low volatile content of PETA relative to HDDA reduces outgassing in vacuum-lamination processes, but the high acrylate functionality requires strict control of photoinitiator concentration to avoid exothermic runaway in thick encapsulation layers.

    Thermal Autoacceleration Emerges in Bulk Photopolymerization

    The free-radical photopolymerization of PETA in bulk or thick sections exhibits autoacceleration. As conversion increases, termination becomes diffusion-controlled while propagation remains relatively mobile; radical concentration rises and reaction rate accelerates. In thick sections exceeding 2–3 mm, this can generate an internal temperature rise sufficient to initiate thermal polymerization after UV exposure ceases. Production-scale stereolithography platforms using PETA-containing resins therefore limit build chamber temperature and use low photoinitiator concentrations. Published data for this specific configuration is limited, but differential scanning calorimetry per ISO 11357-1 can measure exotherm onset and reaction energy; isothermal scans at 25°C show rapid exotherm after a short induction period. Formulators should note that the high acrylate functionality of PETA increases exotherm relative to HDDA and can crack thick castings if cure is not staged. This limitation is managed by partial replacement with difunctional aliphatic diluents or by pulsed UV exposure that allows thermal relaxation between exposures.