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Radical Photoinitiator IGM Omnirad TPO

    • Product Name: Radical Photoinitiator IGM Omnirad TPO
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 879269
    Product Omnirad TPO
    Brand IGM
    Product Type Radical Photoinitiator
    Chemical Name Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide
    Cas Number 75980-60-8
    Molecular Formula C22H21O2P
    Molecular Weight 348.38 g/mol
    Appearance Light yellow crystalline powder
    Odor Mild aromatic odor
    Melting Point Range 88-92 °C
    Purity Hplc ≥98.5%
    Absorption Maxima 295 nm and 380 nm
    Solubility Soluble in acetone, ethyl acetate, toluene, and most acrylate monomers; insoluble in water
    Storage Temperature Store below 25 °C, away from light and humidity

    As an accredited Radical Photoinitiator IGM Omnirad TPO factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Provided as pale yellow crystalline powder packaged in 25 kg fiber drums with inner polyethylene liners for safe storage and handling.
    Container Loading (20′ FCL) One 20′ FCL containing palletized drums of IGM Omnirad TPO radical photoinitiator, securely packed for safe transport.
    Shipping Ship as non-hazardous solid if unclassified, but verify local regulations. Pack in sealed, moisture-proof containers, avoiding light and heat exposure. Use grounded, ventilated transport. Label clearly and include safety data sheets. Ensure compliance with chemical transport laws.
    Storage Store Radical Photoinitiator IGM Omnirad TPO in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep away from strong oxidizing agents and moisture. Maintain temperatures between recommended ranges, avoid unnecessary exposure to light, and inspect containers regularly for damage.
    Shelf Life IGM Omnirad TPO has a shelf life of approximately 2 years when stored unopened, cool, dry, and protected from light.
    Application of Radical Photoinitiator IGM Omnirad TPO

    In sheetfed offset lithographic printing for folding carton and publication stock, Omnirad TPO (CAS 75980-60-8) is incorporated into high-viscosity acrylate ink systems at 2.0–3.5 wt% of total formulation when rutile titanium dioxide loadings are 25–30 wt%. The phosphine oxide is activated by violet and near-UV LED emission at 385 nm, 395 nm, or 405 nm. Its absorption tail above 380 nm is exploited because rutile TiO2 competes less strongly with the photoinitiator at 395 nm than at 365 nm, allowing through-cure of printed ink films. On a sheetfed press fitted with UV LED cassettes, peak irradiance of 12–16 W/cm² and an exposure dose of 300–500 mJ/cm² are commonly targeted for ink films of 1.5–2.5 µm. The ink is milled on a three-roll mill until a grind gauge reading below 10 µm is obtained; TPO is dissolved in the monomer/oligomer phase before pigment addition to avoid undissolved photoinitiator causing plate wear and poor storage stability. During photopolymerization, Type I alpha-cleavage generates a diphenylphosphinoyl radical and a trimethylbenzoyl radical, both of which initiate acrylate polymerization. Surface cure is limited by oxygen inhibition at the ink-air interface; therefore nitrogen blanketing of the sheet path, or addition of an amine acrylate co-initiator at 2–5 wt% of the monomer component, is used. The end products are folding carton exteriors, book covers, and commercial print with cured films showing methylethylketone double-rub resistance above 100 rubs when tested according to ASTM D5402. For packaging intended for direct food contact, TPO is not listed in Annex I of Regulation (EU) 10/2011; the printed article therefore falls under the functional barrier principle of Regulation (EC) 1935/2004, and migration screening by EN 1186-1 with Tenax or modified polyphenylene oxide is necessary. Overdosing above 3.5 wt% may produce residual photoinitiator that exudes to the print surface during post-cure storage at warehouse temperatures above 40°C. Ambient production lighting should be filtered to exclude wavelengths below 450 nm to prevent premature gelation in press-return stock.

    Does Oxygen Inhibition Override TPO Reactivity in Thin-Film Flexographic Whites?

    Thin-film flexographic white inks for shrink sleeves and wraparound labels are discharged through anilox rolls at film weights of 4–8 µm. In these inks, Omnirad TPO is used at 1.5–3.0 wt% of the liquid ink when the formulation contains 15–25 wt% titanium dioxide and a blend of ethoxylated trimethylolpropane triacrylate with difunctional monomers. The low film weight and high surface-to-volume ratio cause severe oxygen quenching of the phosphinoyl radical; cure response therefore depends on peak irradiance rather than total dose alone. LED lamp arrays operating at 385 nm or 395 nm with 8–12 W/cm² peak irradiance are positioned 10–20 mm from the substrate. Under these conditions, press speed is normally limited to 80–150 m/min when TPO is the sole cleavage initiator. Adding an amine-functional acrylate at 3–6 wt% reduces oxygen inhibition, but the amine may increase residual odour and complicate compliance under the Swiss Ordinance for printing inks. The cured ink must withstand substrate shrinkage at 85°C during sleeve application, so adhesion is evaluated by cross-cut tape pull per ISO 2409:2013 after 24 h conditioning at 23°C and 50% RH. Finished products are printed shrink sleeves, wraparound labels, and in-mold labels. RoHS Directive 2011/65/EU Annex II restrictions do not apply to TPO; REACH registration under Regulation (EC) No 1907/2006 is maintained. Direct food contact sleeves are not recommended without a functional barrier because TPO migration is not authorised under EU Regulation 10/2011. In-line viscosity is controlled by adding monomer rather than solvent; viscosity above 1,500 mPa·s at 25°C causes ink misting and plate contamination on long runs.

    Flat-line finishing of medium-density fibreboard, high-density fibreboard, and oak veneer panels uses Omnirad TPO in 100% solids UV-curable clear sealers and pigmented topcoats. Clear sealer formulations typically contain 0.5–1.2 wt% TPO, while pigmented topcoats require 1.0–2.0 wt% depending on colour intensity and hiding power. The coating is applied by roller coater at 20–40 g/m² for clear sealer and 40–80 g/m² for pigmented topcoat. Panels are preheated to 40–50°C to reduce viscosity and improve levelling before UV exposure. Curing is performed with LED lamps at 395 nm or 405 nm, with peak irradiance of 4–6 W/cm² and a dose of 400–800 mJ/cm² for full conversion through the film. The cured coating is tested for pendulum hardness according to ISO 1522, cross-cut adhesion according to ISO 2409:2013, and weathering yellowing under xenon arc per ISO 4892-3. In clear systems, TPO doses above 2.0 wt% may raise the yellowing index after accelerated weathering, limiting use on natural unstained wood where colour stability is critical. Board moisture content should be below 10% before coating to prevent steam blisters during infrared preheating and UV exposure. The end products are kitchen cabinet fronts, office furniture, and interior composite panels. For surfaces that contact food directly, migration risk precludes use without a verified barrier layer. Incompatibility is observed with strong acids and transition metal driers, which can accelerate decomposition of the phosphine oxide and reduce shelf stability of the ready-to-spray mixture.

    When Low-Viscosity Acrylate Laminating Adhesives Require LED Cure at 395 nm

    At 395 nm, clear laminating adhesives based on urethane acrylate oligomers and isobornyl acrylate monomers are more dose-limited than surface-cure coatings because polyethylene terephthalate lamination film absorbs a measurable fraction of the incident radiation below 400 nm. Omnirad TPO is incorporated at 0.4–1.2 wt% of the adhesive mass, with viscosity maintained between 200 and 800 mPa·s at 25°C for gravure or smooth-roll application. Adhesive film thickness after lamination is normally 10–30 µm. A UV dose of 800–1,200 mJ/cm² with peak irradiance of 4–8 W/cm² is typical at line speeds of 20–50 m/min. The major processing limitation is oxygen inhibition at exposed edges; uncured adhesive edges exhibit a visible wet line and lose peel strength. T-peel adhesion is tested according to ASTM D1876 after 24 h at 23°C and 50% RH, with values dependent on film grade and surface treatment; published data for specific film combinations is limited. The end product is a flexible laminate for industrial graphics, window films, and lamination of printed sheets. Compliance is limited to non-food industrial use unless migration testing confirms a functional barrier. Storage of TPO-containing adhesive premixes should avoid temperatures exceeding 35°C because background acrylate polymerisation can slowly raise viscosity. Contact with transition metal driers or strong acids destabilises the phosphine oxide and shortens pot life.

    Resin formulations for vat photopolymerization at 385 nm and 405 nm use Omnirad TPO as a cleavage initiator in multifunctional methacrylate and acrylate matrices. Loading ranges from 0.5–1.5 wt% in clear resins to 1.0–2.5 wt% when fumed silica or ceramic fillers are present. The working curve is described by the Jacobs equation, Cd = Dp ln(E/Ec), where Cd is cure depth, Dp is penetration depth, E is exposure dose, and Ec is critical energy. Critical energy rises with filler concentration and pigment loading, so higher TPO loadings are needed only up to the point where scattering limits dose delivery. In bottom-up LCD or DLP printers with 405 nm LED arrays at 2–4 mW/cm², layer exposure doses are typically 20–80 mJ/cm² for layer thicknesses of 25–100 µm. Overcure produces lateral growth and loss of feature resolution, while residual phosphine oxide contributes to yellowing after thermal post-cure. Printed tensile coupons are conditioned for 24 h at 23°C and tested according to ASTM D638-14. The end products are rapid prototyping parts, thermoform tooling, and dental models. These parts are not suitable for food-contact or medical use unless formulation-specific biocompatibility is established. Ambient light in the resin tank area must be blocked below 450 nm to prevent unintended gelation.

    Conformal Coating Edge Coverage and the 405 nm Absorption Tail

    On assembled printed circuit boards, selective spray application of UV-curable acrylated urethane coatings uses TPO at 0.5–1.5 wt% in clear formulations for needle dispensing or spray valve coating. The coating process applies 25–75 µm wet film. Cure is conducted in two stages: a tack-free LED surface cure at 395 nm with 2–4 W/cm², followed by dark storage or low-temperature aging at 40°C for 24 h to complete dark polymerisation. The 405 nm absorption tail improves cure in low-shadow zones, but completely shadowed regions under large components remain uncured and rely on dark cure rather than radiation. The cured coating is tested per IPC-CC-830B, including hydrolytic stability at 85°C and 85% RH, insulation resistance after 168 h, and flammability according to UL 94 V-0. Volatile condensable materials are measured by headspace GC-MS where service temperatures exceed 125°C because phosphine oxide photolysis can release residual benzaldehyde. The product is a protective conformal coating on power supplies, LED drivers, and industrial controllers. The coating must not be applied to bare silver electrodes because phosphine oxide can coordinate with silver ions and create haze or interfacial adhesion loss. REACH registration under Regulation (EC) No 1907/2006 applies to the raw photoinitiator; the formulated coating must be assessed for specific customer workplace exposure scenarios.

    For high-opacity screen printing on flame-retardant polycarbonate and poly(methyl methacrylate), Omnirad TPO is dissolved into solvent-free UV screen ink formulations at 2.5–4.0 wt% when the cured legend is white, light-coloured, or metallised. The ink is printed on a flatbed or cylinder screen press through mesh counts of 120–165 threads/cm, producing a wet deposit of 15–25 µm. The substrate surface is pre-cleaned and corona-treated where necessary to raise wetting tension above 40 mN/m. Curing is carried out with LED lamps at 405 nm, with peak irradiance of 6–10 W/cm² and a dose of 800–1,200 mJ/cm² because thick screen deposits absorb strongly and the surface layer is oxygen-inhibited. Adhesion is tested according to ASTM D3359-17 after 72 h conditioning at 23°C and 50% RH. Chemical resistance is evaluated by ASTM D1308 against ethanol and gasoline for automotive service; published performance values depend on substrate grade and ink pigment. The end products are instrument panel graphics, membrane switch overlays, and warning legends on flame-retardant sheet. RoHS Directive 2011/65/EU applies to the finished electrical or electronic article, and the screen ink must be evaluated in the complete assembly. Water-based screen practice is not recommended because TPO has low water solubility and may separate in humid screen rooms above 60% RH, causing pinholing and uneven cure.

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    Certification & Compliance
    More Introduction
    Radical Photoinitiator IGM Omnirad TPO is a monoacylphosphine oxide supplied as a yellowish crystalline powder and identified by CAS 75980-60-8. The active molecule, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, has a molecular mass of 348.4 g/mol. Differential scanning calorimetry conducted in accordance with ASTM E794-06(2018) records a melting endotherm between 88 °C and 92 °C; storage in closed containers below 35 °C with protection from moisture, direct sunlight, and thermal cycling is required. The material functions as a Norrish Type I radical photoinitiator that undergoes α-cleavage upon ultraviolet exposure, generating 2,4,6-trimethylbenzoyl and diphenylphosphinoyl radical species without amine co-initiators. The acylphosphine oxide chromophore differs from α-hydroxy ketone photoinitiators such as Omnirad 1173 in that it absorbs at longer wavelengths. Published solution spectra show principal absorption bands near 295 nm, 368 nm, 380 nm, and 393 nm in acetonitrile, with a tail extending beyond 420 nm. This behavior permits response under the 365 nm, 385 nm, 395 nm, and 405 nm emission lines used in mercury-arc and UV-LED curing lines. The powder is added at concentration ranges reported as 0.5–3.0 wt% for clear UV-cured formulations and 1.0–4.0 wt% for pigmented systems, although the optimum is formulation-dependent.
    Typical technical parameters reported for IGM Omnirad TPO
    ParameterTypical valueMethod or condition
    CAS registry number75980-60-8
    Chemical classmonoacylphosphine oxide
    Physical formyellowish crystalline powdervisual inspection at 25 °C
    Molecular mass348.4 g/molcalculated from molecular formula
    Melting range88–92 °Cdifferential scanning calorimetry, ASTM E794-06(2018)
    Principal absorption maxima295 nm, 368 nm, 380 nm, 393 nmacetonitrile solution, UV-Vis spectrophotometry
    Recommended storagebelow 35 °C, dry, closed containermanufacturer storage guidance

    How does the acylphosphine oxide chromophore alter through-cure response in pigmented films?

    In white-pigmented acrylate coatings containing titanium dioxide at 12–25 wt% and film thickness between 25 µm and 75 µm, shorter-wave ultraviolet radiation is strongly attenuated by pigment scattering and absorption. The long-wavelength tail of TPO allows a larger fraction of incident radiation to reach the lower portion of the film. Published starting-point formulations therefore place TPO at 1.0–3.0 wt% on total resin solids to afford through-cure without amine synergists. Photolysis products are partially photobleaching, reducing internal filter effects as conversion proceeds. This characteristic is the main reason the product is specified for white basecoats, high-opacity screen inks, and pigmented wood coatings where a conventional α-hydroxy ketone would leave an uncured interface or require post-cure. Surface cure in such systems remains subject to oxygen inhibition because molecular oxygen competes with acrylate radicals at the coating-air boundary. In formulations where surface tack is observed at low line speed, TPO is normally combined with a Norrish Type II photoinitiator or with an α-hydroxy ketone such as Omnirad 184 or Omnirad 1173; the selection is governed by lamp type, film weight, and pigment volume concentration. The replacement ratio is not direct because TPO has a lower molar extinction coefficient in the UVC range but higher absorbance at 380–420 nm. Production data from UV-curable clear topcoats applied by roll coater at 10–20 g/m² wet film weight indicate that TPO when used as the sole photoinitiator at 1.5–2.0 wt% can produce tack-free surfaces under 385 nm LED arrays at peak irradiance of 8–16 W/cm², provided line speed is adjusted to produce a UV dose of approximately 800–1,500 mJ/cm². Published data for each specific resin and pigment combination remain limited; dose mapping with radiometers calibrated to the specific emitter wavelength is required before changing from mercury-arc to LED sources. Photopolymerization kinetics for TPO in acrylate monomers are typically characterized by real-time Fourier transform infrared spectroscopy. In tripropylene glycol diacrylate at 3 mm thickness, the acylphosphine oxide produces lower initial radical flux than Omnirad 819 but longer-lived through-cure because photobleaching decreases internal filtering. The polymerization rate is proportional to the square root of light intensity in the steady-state bimolecular termination regime; doubling peak irradiance from 4 W/cm² to 8 W/cm² therefore increases cure speed by approximately 1.4 times, not 2 times. This behavior matters in high-speed flexo and inkjet lines where marginal dose changes control tack-free cure. On production lines, TPO is generally predissolved in monomer or oligomer before blending to prevent crystalline deposits on pump filters, static mixers, and roll-coater trays. Batch records from high-viscosity epoxy acrylate lines show that additions above 2.0 wt% to an epoxy acrylate bisphenol A diacrylate blend without pre-dissolution can form visible deposits when letdown temperature falls below 20 °C. Heating the predispersion to 40–50 °C under shear in a closed vessel reduces the risk of recrystallization. In UV-curable powder coating production, TPO is dry-blended before extrusion on a twin-screw extruder; melt temperatures above 100 °C are avoided to prevent premature decomposition and uncontrolled crosslinking during the extrusion stage. The actual temperature limit depends on dwell time, screw geometry, and antioxidant package.

    If a formulation migrates from medium-pressure mercury arcs to 395 nm LED arrays

    Mercury vapour lamps emit polychromatic output with prominent lines at 365 nm, 404.7 nm, and 435.8 nm, whereas UV-LED arrays emit a narrow emission band with full width at half maximum commonly below 20 nm. A 395 nm LED line therefore removes the shorter-wave photons that contribute to surface cure in many α-hydroxy ketone formulations and reduces the photon flux at wavelengths where TPO has its strongest absorption. When the same TPO loading is retained, the result may be lower double-bond conversion at the substrate interface, increased residual monomer, and slower hardness development. Reformulation for 395 nm LED should include an increase in acylphosphine oxide content or a combination with a bis-acylphosphine oxide photoinitiator when through-cure requirements are severe. Radiometric monitoring is mandatory because UV-LED array output changes with junction temperature, aging, and current control. A UV radiometer calibrated at the specific emitter wavelength should be used to verify peak irradiance and dose after each lamp maintenance interval. In UV-LED flexo printing, TPO at 1.2–2.5 wt% in cyan, magenta, and black inks is common when the press uses LED arrays at 385–405 nm; yellow and white inks often require higher loadings because pigments compete more strongly with the photoinitiator for available photons.
    Comparative characteristics of selected Omnirad photoinitiators
    AttributeOmnirad TPOOmnirad 819Omnirad 1173
    Classmonoacylphosphine oxidebis-acylphosphine oxideα-hydroxy ketone
    Absorption range380–420 nm tail370–450 nm tail230–340 nm principal
    Typical addition range0.5–3.0 wt% clear; 1.0–4.0 wt% pigmented0.3–1.5 wt%1.0–4.0 wt%
    Yellowing tendencymoderatehigherlow
    Through-cure in pigmented filmshighvery highlimited
    Typical combinationwith α-hydroxy ketone or Type IIwith TPO or α-hydroxy ketonewith amine synergist or acylphosphine oxide

    Migration resistance and yellowing-index differences versus bis-acylphosphine oxide in laminating adhesives

    Compared with bis-acylphosphine oxide photoinitiators such as Omnirad 819, TPO has a shorter visible absorption tail and a different photoproduct distribution. In clear acrylate films cured to equivalent conversion, formulations containing TPO generally exhibit lower post-cure yellowing than those containing Omnirad 819 under accelerated UVA exposure according to ASTM G154-16. This difference is formulation-dependent and cannot be used as a standalone specification. TPO also shows more limited absorption beyond 430 nm, which can reduce unwanted visible-light sensitivity during processing and storage; however, the same property makes it less responsive than Omnirad 819 in very thick white laminates or dental restoration resins where longer-wavelength photon penetration is critical. Residual photoinitiator migration must be evaluated before use in indirect food-contact printed matter. Published regulatory data for TPO are jurisdiction-specific; a printed or coated article intended for food contact requires worst-case migration testing under the applicable framework, such as Regulation (EU) No 10/2011 for plastics or FDA 21 CFR 175.300 for resinous and polymeric coatings, unless the substance is otherwise authorized for the use. In applications where migration limits are low, the formulation should be optimized for maximum conversion and the residual unreacted photoinitiator measured by high-performance liquid chromatography with UV detection. The limit of quantification should be established for the specific food simulant and contact ratio; published data for this specific configuration are limited. Typical application areas include UV-curable screen inks, offset inks, overprint varnishes, clear and white-pigmented wood coatings, plastic topcoats, and structural adhesives. In UV screen inks, the product is usually dispersed with the pigment grind rather than added as a post-additive to limit localized concentration gradients. In UV-LED laminating adhesives for flexible packaging, through-cure is monitored by infrared spectroscopy according to ASTM E1252-98(2021) by following the disappearance of the acrylate double bond near 810 cm⁻¹ and 1630 cm⁻¹; conversion below 70% may increase the risk of delamination and odor in the laminate. Formulators should verify cure at the substrate interface because surface tack can be absent while the buried layer remains undercured. Oxygen inhibition at the coating surface is governed by competition between dissolved molecular oxygen and acrylate radicals. Dissolved oxygen concentration in common acrylate monomers is commonly reported on the order of 1–10 mmol/L at ambient pressure. Each oxygen molecule can scavenge multiple radicals through peroxy radical formation. TPO does not eliminate this effect. Surface cure can be improved by nitrogen inerting to maintain residual oxygen below 0.1% in the curing chamber, increasing initiator loading, or applying a barrier layer in offset inks. These methods require validation for each film weight and line speed. In UV-curable wood coatings, TPO is used when both through-cure and limited yellowing are required under clear topcoats applied at 80–120 g/m². The exact level is controlled by wood stain type, UV absorber content, and sanding sequence. When the formulation includes UV absorbers or hindered amine light stabilizers, the photoinitiator concentration must be increased because these additives compete for photons in the 300–420 nm region. Published data for specific UV absorber packages are limited; laboratory cure-dose arrays are required to confirm the processing window. Digital light processing resins containing TPO at 0.2–0.5 wt% in acrylate or methacrylate matrices cure at 385–405 nm; lower loadings reduce light scattering in high-resolution builds. Residual photoinitiator can migrate from printed parts; in medical device applications, ISO 10993 biocompatibility testing is required for the final polymerized article because the photocured part is not equivalent to the raw photoinitiator. In UV-curable adhesive bonding of glass and polycarbonate, through-cure behind light-blocking substrates is not possible with TPO alone because the initiator requires direct UV exposure. Dual-cure systems combining UV-initiated radical polymerization with moisture or thermal cure are used where light access is incomplete. Joint designs with UV-transmissive substrates and bondline thickness below 0.5 mm are generally processable with TPO-containing adhesives when the UV source delivers sufficient dose through the substrate. Compatibility with polycarbonate must be checked because aromatic solvents and certain monomers can induce environmental stress cracking.
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