| HS Code | 490113 |
| Product Name | BASF Irgacure 369 |
| Chemical Name | 2-Benzyl-2-(dimethylamino)-1-[4-(4-morpholinyl)phenyl]-1-butanone |
| Cas Number | 119313-12-3 |
| Molecular Formula | C23H30N2O2 |
| Molecular Weight | 366.5 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 110-115 °C |
| Density | 1.19 g/cm³ at 20 °C |
| Absorption Maxima | 233 nm, 254 nm, 323 nm |
| Solubility | Soluble in acetone, tetrahydrofuran, methanol, and toluene; insoluble in water |
| Storage Temperature | Store below 25 °C in a cool, dry place |
| Shelf Life | At least 12 months under recommended storage conditions |
| Photoinitiator Type | Type I free-radical photoinitiator (alpha-amino ketone) |
As an accredited Radical Photoinitiator BASF Irgacure 369 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | BASF Irgacure 369 radical photoinitiator is packaged as yellow powder in 20 kg sealed containers to maintain stability and safety. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with drums of BASF Irgacure 369, safely secured, labeled, and stowed per chemical transport regulations. |
| Shipping | For shipping, BASF Irgacure 369 (2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)butan-1-one; CAS 119313-12-1) is not regulated as dangerous goods. It should be packed in sealed, light-protected containers, kept dry, away from heat, sparks, and UV exposure. No UN number or hazard transport label is required. |
| Storage | Store Radical Photoinitiator BASF Irgacure 369 in its original, tightly closed container in a cool, dry, well-ventilated area. Protect from direct sunlight, heat, and ignition sources. Keep away from strong oxidizers and incompatible materials. Ensure the area is clean and containers are clearly labeled to prevent contamination and moisture ingress. |
| Shelf Life | Unopened, stored below 40°C, protected from light and moisture, Irgacure 369 has a shelf life of at least 2 years. |
Irgacure 369 is an α-amino ketone radical photoinitiator based on 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)butan-1-one, with molar mass 366.5 g/mol, melting range 110–115 °C, and a methanolic absorption maximum near 324 nm that extends into the 365 nm mercury emission band. The crystalline powder has limited water solubility and is therefore introduced through acrylate monomer, ketone, or ester pre-dissolution rather than direct aqueous dispersion. The material is incorporated into acrylate-functional UV-curable formulations where photoinitiator selection must account for pigment absorption, oxygen inhibition, film thickness, lamp type, and migration limits. Application-specific addition ratios and process boundaries are set by the curing geometry, not by a single generic dosage.
UV lithographic inks formulated for sheetfed offset presses typically contain high pigment volume concentrations and require photoinitiator packages that maintain through-cure at press speeds above 12,000 sheets/h. In this environment Irgacure 369 is used at 3.0–6.0 wt% of total ink mass, commonly with 1.0–3.0 wt% of 2-isopropylthioxanthone to extend the absorption envelope at 365 nm and 385 nm. The α-amino ketone is dissolved in acrylate diluents before incorporation because its melting range of 110–115 °C can generate crystalline residues if dry powder is added directly during high-speed dispersion. Compliance for commercial offset inks is assessed under REACH Regulation (EC) No 1907/2006, while print process control follows ISO 12647-2:2013 and ink colorimetry follows ISO 2846-1:2017. For printed matter that may contact food through a functional barrier, formulation components are screened under the EuPIA Good Manufacturing Practice and the Swiss Ordinance SR 817.023.21; Irgacure 369 is not recommended for direct food-contact ink without migration testing.
Ink manufacturing for this segment proceeds through a high-speed disperser followed by a three-roll mill, with rolls maintained at 25–35 °C to keep the mill base below radical generation temperature. The mill gap is adjusted to produce a final grind below 5 µm, and vacuum deaeration is applied to prevent microfoam from reducing optical density. On a sheetfed press, the UV curing unit is positioned after the delivery or between printing units; lamp irradiance is typically 120–180 W/cm in the 300–400 nm band, and the reflector geometry is selected to maintain peak irradiance without overheating the substrate. The printed and cured film is subjected to tape adhesion and rub resistance tests according to ASTM D3359-17 and a modified Sutherland rub test, because matt and dark pantone inks using Irgacure 369 at the upper addition window can exhibit residual amine at the film surface if under-cured. Terminal article types include folding cartons for cosmetics and pharmaceuticals, book covers, direct mail covers, and printed metal decorating blanks for beverage and confectionery tins.
In narrow-web flexo, the anilox roller deposits inks with cell volumes between 2.5 BCM and 4.0 BCM and line counts of 800–1,200 LPI, yielding wet films of 6–12 µm; this low film weight creates a high surface-to-volume ratio in which oxygen inhibition consumes radicals at the surface. Irgacure 369 is employed at 3.5–7.0 wt% of total formulation in TiO₂-containing whites and carbon-black blacks, while lighter monochromatic inks are formulated at 2.0–4.0 wt% to limit yellowing and residual amine odour. In heavily pigmented grades, a thioxanthone derivative such as 2-isopropylthioxanthone is added at 0.5–2.0 wt% to improve through-cure under the 365 nm emission line of doped mercury lamps. Print process control is based on ISO 12647-6:2020; raw material and finished ink compliance is managed under REACH 1907/2006, and for low-odour shrink sleeve and label applications the Swiss Ordinance SR 817.023.21 migratables framework is applied.
Production of UV flexo ink concentrates is carried out in bead mills or high-shear batch mixers, with pigment grinds below 5 µm and viscosity adjusted to 50–250 mPa·s for chambered doctor-blade application. The press configuration often includes UV lamp modules rated 8–16 kW and inerting is not usually employed; therefore the photoinitiator package must compensate for oxygen diffusion. Irgacure 369 is pre-dissolved in acrylate monomer under yellow lighting before the final letdown, and the millbase is maintained below 35 °C to prevent premature polymerization at hot spots. Cure adequacy is monitored by methyl ethyl ketone double rubs or by ATR-FTIR acrylate conversion at the print surface. Terminal converted articles include pressure-sensitive labels for beverage and durables, shrink sleeves for PET containers, flexible packaging pouches for non-food and food-contact applications requiring a functional barrier, and thermal transfer label overprint webs.
For membrane switch overlays and appliance panels, screen-ink formulations are applied as thixotropic films that are deposited through mesh openings and then subjected to UV exposure in conveyorized tunnels. Irgacure 369 is added at 2.5–5.0 wt% of total ink mass; the exact amount is set by mesh count, film thickness and pigment type. At the lower end, clear conductive dielectric overlays are used, while black and white graphic layers with heavy pigmentation require the upper end. The ink is manufactured on a triple-roll mill with temperature-controlled rolls, and the grind gauge reading is held below 15 µm to avoid mesh clogging. Compliance testing for cured prints on polyester and polycarbonate includes cross-hatch adhesion according to ASTM D3359-17 Method B and pencil hardness according to ASTM D3363-20; the finished membrane switch assemblies are evaluated under ISO 1518-1:2019 scratch resistance or equivalent OEM specifications.
The downstream process uses screens with 90–150 threads/cm and squeegee durometer 60–85 Shore A, with an off-contact distance of 1.0–2.5 mm for graphics and 0.5–1.0 mm for conductive silver traces when combined with UV dielectric layers. The wet film thickness after screen printing is commonly 15–35 µm, significantly higher than flexo or offset, which reduces surface-to-volume cure stress but increases sensitivity to bulk absorption; Irgacure 369’s UV-A activity is used to maintain cure through pigmented graphic blacks. Conveyorized UV tunnels are set to 80–120 W/cm with belt speed 5–15 m/min, and curing dose is referenced to a calibrated radiometer operating in the 320–390 nm band. Production handling requires exclusion of ambient white light because the photoinitiator has long-wavelength sensitivity; stock is stored at ≤30 °C and <40% RH in sealed containers. Terminal product types include membrane switch overlays, industrial nameplates, in-mold decoration inserts for appliance fascia, and UV-cured screen-printed polycarbonate panels for medical display housings.
For white cabinetry coatings, the critical variable is the UV competition between TiO₂ pigment and photoinitiator at 365 nm; titanium dioxide absorbs strongly below 380 nm, while Irgacure 369 has sufficient UV-A absorption to initiate polymerization beneath the pigmented film surface. Addition ratios range from 2.0–4.5 wt% in transparent grain fillers and sanding sealers to 3.0–6.0 wt% in white pigmented topcoats and opaque primers. In high-build white formulations, a bisacylphosphine oxide photoinitiator is co-added at 0.5–2.0 wt% to maintain surface cure and reduce oxygen inhibition; the combination is dissolved in acrylate oligomers under low shear. Cured coating durability is tested under ASTM D3359-17 for adhesion, ASTM D523-14(2021) for specular gloss, and DIN 68861-1 for furniture surface resistance to chemical agents.
Application on flat panels is performed with roller coaters or curtain coaters at coating weights of 15–40 g/m², followed by UV curing units equipped with medium-pressure mercury lamps at 100–160 W/cm; the lamps are arranged in a dual-bank configuration to deliver a total UV dose of 300–800 mJ/cm² in the UV-A band. The high film weight and white pigmentation require that line speed be derated relative to clear coatings, otherwise the lower layers remain under-cured and show post-embrittlement or delayed oil exudation. In sanding sealer operations, the first UV pass is partially cured and sanded with 320–400 grit abrasive before topcoat; incomplete through-cure at this stage causes clogging of sanding belts and exaggerated grain raising. Irgacure 369 is pre-dissolved in monomer at 40–50 °C under light-safe conditions before addition to the coating batch. Terminal finished products include kitchen cabinet doors, office furniture panels, flat-pack furniture components, and UV-primed wood flooring substrates.
After surface activation of PC/ABS substrates, robotic spray lines apply UV-curable coatings at dry film thicknesses of 10–20 µm, where the photoinitiator package must deliver both surface cure and film-through cure without generating residual odour or extractable amine. Irgacure 369 is used at 2.0–5.0 wt% of total coating formulation, with the lower end reserved for transparent clearcoats and the upper end for black or metallic pigmented layers that absorb strongly across the UV-A band. Adhesion is qualified according to ISO 2409:2020 cross-cut classification 0–1, and pencil hardness is measured under ISO 15184:2020; chemical resistance is assessed with ASTM D1308-20 spot tests using artificial sebum, sunscreen lotion, and automotive interior cleaners.
Surface activation of the plastic substrate is performed by atmospheric plasma or low-pressure UV and is controlled to a surface energy of 56–64 mN/m before coating application. The coating is applied in water-wash spray booths, flashed at 40–50 °C for 5–10 min, and cured under focused elliptical reflector lamps rated 80–120 W/cm with a peak irradiance of 200–600 mW/cm² in the UV-A band. The use of Irgacure 369 in pigmented systems is typically paired with acylphosphine oxide photoinitiators at 0.5–2.0 wt% to support surface cure, while the α-amino ketone maintains deep conversion in shaded areas near part edges. Production control includes periodic ATR-FTIR acrylate unsaturation checks and methyl ethyl ketone rub testing after ageing at 60 °C for 72 h. Terminal product types comprise automotive centre console trim, steering wheel bezels, consumer electronics housings, cosmetic compacts, and scratch-resistant covers for medical diagnostic devices.
In adhesive lamination, the competing requirement is that UV radiation must pass through a transparent substrate or penetrate pigmented adhesive bulk to generate sufficient radical flux at the opposite interface. Irgacure 369 is employed at 0.5–2.5 wt% of total adhesive formulation in clear laminating adhesives for PET, BOPP and PVC films, and at 1.5–3.0 wt% in pigmented or UV-absorbing assembly adhesives for rigid polymer components. The addition ratio is kept below the solubility limit in the chosen acrylic or urethane acrylate oligomer mixture, and the photoinitiator is dissolved at 40–50 °C before compounding to prevent particulate contamination in nip coaters. Compliance for structural and laminating adhesives is tested under ISO 4587:2019 for lap-shear strength of bonded metal or plastic specimens and ASTM D1876-19 for T-peel resistance of flexible laminates; for indirect food-contact packaging, the adhesive film is assessed under FDA 21 CFR 175.105 conditions or EU Regulation 10/2011 with a demonstrated functional barrier.
Processing is carried out on a laminating line with a gravure or slot-die application station, a nip pressure of 2–4 bar, and UV curing through the transparent web using an LED lamp at 365 nm or a doped mercury lamp with a UV-A reflector. When the adhesive contains pigments or fillers, a 385 nm LED source is preferred because longer-wavelength radiation penetrates deeper into the bondline and reduces the surface-to-depth cure gradient. The irradiance at the adhesive plane is monitored with a calibrated radiometer, and the line speed is adjusted to maintain a UV-A dose of 400–1,200 mJ/cm². For UV-LED curing of clear adhesives, Irgacure 369 may be supplemented with thioxanthone at 0.3–1.0 wt% because the α-amino ketone alone has moderate absorbance at 385 nm. Fully cured laminates are subjected to heat-ageing at 50 °C for 72 h followed by re-testing of peel adhesion to detect post-cure drift. Terminal finished products include pressure-sensitive label stocks, film-to-film lamination pouches, optical display bonding gaskets, and rigid plastic assembly adhesives for medical device housings where published data on long-term skin contact for this specific configuration is limited and must be generated under ISO 10993-1.
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Radical photoinitiator BASF Irgacure 369 is the commercial designation for 2-benzyl-2-(dimethylamino)-4'-morpholinobutyrophenone, CAS 119313-12-2. The compound is a Norrish Type I alpha-amino ketone supplied as a pale yellow crystalline powder with a molar mass of 366.50 g/mol and a supplier-listed melting range of 110–117 °C. HPLC assay is specified at not less than 99.0%, with volatile matter not more than 0.2%. The tertiary amine located beta to the carbonyl undergoes alpha-cleavage after UV absorption, releasing a benzoyl radical and a tertiary aminoalkyl radical. The aminoalkyl species reduces the severity of oxygen inhibition at the coating surface, while the morpholinophenyl substituent red-shifts absorption into the near UV and visible blue range. The BASF designation remains the industrial reference, although the photoinitiator business historically associated with Ciba Specialty Chemicals and BASF is now manufactured and distributed by IGM Resins under the same trade name.
In methanol, the primary absorption maximum appears near 325 nm, with an absorption tail that extends past 400 nm. The electron-donating morpholino group at the para position of the phenyl ring and the dimethylamino group alpha to the carbonyl broaden the conjugated system relative to the methylthio-substituted analog Irgacure 907. Under broadband medium-pressure mercury arc lamps, the 365 nm i-line is therefore more efficiently captured than by alpha-hydroxy ketones such as Irgacure 184. The photochemical cleavage is monomolecular; no amine co-initiator is required for polymerization of acrylate monomers. The benzoyl radical initiates chain growth, while the tertiary aminoalkyl radical acts as a surface-active species that consumes dissolved oxygen and can improve tack-free cure in air. In clear films, nitrogen-containing photoproducts may contribute to yellowing after long ultraviolet exposure; this effect is formulation-dependent and should be screened by accelerated weathering according to ISO 4892-2:2013 or ASTM D4587-11.
| Photoinitiator | CAS registry number | Molar mass | Primary absorption maximum | General function |
|---|---|---|---|---|
| Irgacure 369 | 119313-12-2 | 366.50 g/mol | 325 nm | Norrish Type I alpha-amino ketone; long-wavelength through-cure |
| Irgacure 907 | 71868-10-5 | 279.39 g/mol | 306 nm | Norrish Type I alpha-amino ketone; pigmented inks |
| Irgacure 184 | 947-19-3 | 204.26 g/mol | 246 nm | Norrish Type I alpha-hydroxy ketone; clear coatings |
| TPO | 75980-60-8 | 348.37 g/mol | 380 nm | Acylphosphine oxide; white UV-LED cure |
Across UV-curable graphic arts applications, Irgacure 369 is introduced into acrylate and methacrylate monomer blends at concentrations ranging from 0.5 wt% to 5.0 wt% based on total formulation solids. In pigmented screen inks and solder masks, the total photoinitiator package is typically elevated to 4.0 wt%–7.0 wt% and is often combined with isopropylthioxanthone to extend absorption at the 365 nm and 405 nm exposure lines. The product is dissolved in tripropylene glycol diacrylate, trimethylolpropane triacrylate, or aromatic solvent blends before high-shear dispersion; the crystalline powder requires heating to 40–50 °C under amber light and moderate agitation for complete dissolution. In solventless systems, the viscosity contribution at 2.0 wt% is small but measurable by cone-and-plate viscometry.
In dry film photoresists for printed circuit board processing, Irgacure 369 is used because its absorption tail covers the ultraviolet laser direct imaging wavelengths of 355 nm and 405 nm. In negative-tone dry films exposed on laser direct imaging systems operating at 355 nm or 405 nm, the photoinitiator participates in free-radical crosslinking of acrylic photopolymers to produce the solubility differential required for alkaline development in 1.0 wt% sodium carbonate solution at 30 °C. The processing window is narrow; under-exposure creates residual soft film and adhesion loss, while over-exposure leads to pattern widening and reduced resolution. Solder mask formulations require through-cure through 20–25 µm dry film thickness, and cure dose is commonly benchmarked by solvent rub testing according to ASTM D5402-15. Adhesion after cure is assessed by cross-hatch ISO 2409:2013 or ASTM D3359-09ε2. On horizontal conveyorized exposure units using medium-pressure mercury arc lamps at intensities up to 200 W/cm, hold times between coating and exposure are commonly held between 15 min and 30 min to avoid surface re-equilibration. Published data for this specific configuration is limited; formulators must verify through-cure and adhesion on each substrate because variations in filler loading and pigmentation shift the effective penetration depth.
In UV-curable wood sealers and topcoats, the addition of Irgacure 369 at 1.0–3.0 wt% increases through-cure in grain pores and at the base of matting agent particles. Adhesion to sanded oak or beech substrates can be assessed by ISO 2409:2013, while scratch resistance is measured by ISO 15184:2020. Gloss reduction from matting agents makes through-cure measurements more critical; solvent rub ASTM D5402-15 is used to detect under-cured regions. In UV-curable adhesive lamination, coating weights of 5–15 g/m² on polyester or polypropylene film require through-cure sufficient to support bond strength testing according to ASTM D1876-08. Irgacure 369 is blended with alpha-hydroxy ketones or acylphosphine oxides in these formulations because the optical density at the film surface must be kept below the level that causes excessive top-surface polymerization and poor interlayer adhesion.
Replacement of Irgacure 907 with Irgacure 369 changes the absorption profile and the migration behavior. The molar mass increase from 279.39 g/mol for Irgacure 907 to 366.50 g/mol for Irgacure 369 reduces the free-volume diffusion coefficient in cured acrylate networks, which is relevant for low-odour and low-migration printing applications. The primary absorption maximum shifts from 306 nm to 325 nm, improving response at the 365 nm emission band but requiring reformulation of the top-surface cure, which can be partially compensated by the addition of 0.5–1.0 wt% of a benzophenone derivative or by higher lamp irradiance. The sulfur-containing chromophore of Irgacure 907 is absent in Irgacure 369; this reduces sulfur-related volatile degradation products but changes the odour profile rather than eliminating it entirely. In yellow and magenta screen inks, the longer-wavelength absorption can be disadvantageous because more photons are absorbed in the surface layer, and pigment interference at 325 nm may require a higher total photoinitiator loading.
Unlike benzophenone-amine two-component systems, Irgacure 369 does not require a hydrogen-donating co-initiator for radical generation. This monomolecular mode simplifies formulation because the amine co-initiator concentration no longer controls surface cure, and the risk of amine bloom in the cured film is reduced. However, benzophenone remains favored in clear pressure-sensitive adhesives where low color and controlled surface cure dominate; Irgacure 369 is selected when the process demands through-cure of pigmented or thick sections.
The crystalline powder is stable under recommended storage conditions but softens and cakes when exposed to temperatures above 40 °C. The supplier lists a melting range of 110–117 °C; heating beyond the melting point initiates thermal decomposition and should be avoided. The product is insoluble in water and dissolves in common ketones, esters, ethers, and acrylate monomers. Solubility in aliphatic hydrocarbons is low. In solventless monomer blends, dissolution is performed at 40–50 °C with moderate shear; exposure to UV light during compounding must be minimized because the photoinitiator can generate radicals and trigger unwanted polymerization. Storage in airtight HDPE containers under nitrogen or dry air is required when relative humidity exceeds 60% to prevent moisture-induced caking. The material safety data sheet assigns no explosive or oxidizing properties, but the compound is classified as hazardous to the aquatic environment and must not be discharged to surface water. Formulations below pH 5.0 may protonate the tertiary amine and reduce photoinitiation efficiency; no published kinetic data quantify this effect for Irgacure 369 specifically, so pre-production screening is necessary. Strongly acidic adhesion promoters, chlorinated solvents, and some metal salts can destabilize the alpha-amino ketone during storage or accelerate dark reactions.
Before final specification, end users evaluate the photoinitiator as part of the formulated article under the applicable regulatory and performance framework. The following matrix summarizes common assessment tools.
| Regulation or test standard | Designation | Application in Irgacure 369 evaluation |
|---|---|---|
| REACH Regulation | EC 1907/2006 | Substance registration and SVHC screening; Irgacure 369 is not listed as a substance of very high concern on the candidate list. |
| RoHS Directive | Directive 2011/65/EU | Pure substance is outside the scope; restrictions apply to the finished electrical equipment at homogeneous material level. |
| Adhesion by tape test | ASTM D3359-09ε2 | Used for printed and coated films on metal and polymer substrates after UV cure. |
| Cross-cut adhesion | ISO 2409:2013 | Used for coating-substrate compatibility after UV cure and after thermal stress. |
| Solvent rub resistance | ASTM D5402-15 | Used as a through-cure index for UV-curable inks and coatings. |
| Peel resistance of adhesives | ASTM D1876-08 | Used to measure bond strength in UV-curable adhesive lamination systems containing Irgacure 369. |
| Accelerated weathering | ISO 4892-2:2013 | Used to assess yellowing and gloss retention of clear coats containing nitrogen-based photoinitiators. |
| Color difference | ASTM D2244-15 | Used to quantify delta b* and delta E changes after weathering or thermal exposure. |
On production-scale UV curing lines, the required dose for full cure depends on film thickness, pigment loading, and lamp emission. Formulators use a medium-pressure mercury arc spectrum with major emission lines at 254 nm, 313 nm, 365 nm, 405 nm, and 436 nm; Irgacure 369 couples most efficiently at 365 nm and weakly at 405 nm. For a 20 µm pigmented solder mask layer, through-cure is often established when solvent rub resistance exceeds 50 double rubs according to ASTM D5402-15, but the exact value is formulation-specific. Adhesion to copper-clad FR-4 is screened with ISO 2409:2013 after thermal stress; the cross-hatch classification must not exceed 1 for solder mask acceptance under IPC SM-840E. In clear coatings, yellowing is quantified by delta b* using ASTM D2244-15; the amino ketone photoproducts can raise delta b* after prolonged accelerated weathering, depending on the stabilizer package. Formulations containing Irgacure 369 should not be combined with strongly acidic additives that protonate the tertiary amine, as this can reduce photoactivity; similarly, combinations with certain strong oxidizing agents may cause premature radical generation during storage.