| 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 | 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. |
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.
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.
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.
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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| Parameter | Typical value | Method or condition |
|---|---|---|
| CAS registry number | 75980-60-8 | — |
| Chemical class | monoacylphosphine oxide | — |
| Physical form | yellowish crystalline powder | visual inspection at 25 °C |
| Molecular mass | 348.4 g/mol | calculated from molecular formula |
| Melting range | 88–92 °C | differential scanning calorimetry, ASTM E794-06(2018) |
| Principal absorption maxima | 295 nm, 368 nm, 380 nm, 393 nm | acetonitrile solution, UV-Vis spectrophotometry |
| Recommended storage | below 35 °C, dry, closed container | manufacturer storage guidance |
| Attribute | Omnirad TPO | Omnirad 819 | Omnirad 1173 |
|---|---|---|---|
| Class | monoacylphosphine oxide | bis-acylphosphine oxide | α-hydroxy ketone |
| Absorption range | 380–420 nm tail | 370–450 nm tail | 230–340 nm principal |
| Typical addition range | 0.5–3.0 wt% clear; 1.0–4.0 wt% pigmented | 0.3–1.5 wt% | 1.0–4.0 wt% |
| Yellowing tendency | moderate | higher | low |
| Through-cure in pigmented films | high | very high | limited |
| Typical combination | with α-hydroxy ketone or Type II | with TPO or α-hydroxy ketone | with amine synergist or acylphosphine oxide |