| HS Code | 618504 |
| Product Name | Photoresist Special Photoinitiator |
| Brand | J&K Scientific |
| Iupac Name | 2-Methyl-1-[4-(methylthio)phenyl]-2-(4-morpholinyl)-1-propanone |
| Cas Number | 71868-10-5 |
| Molecular Formula | C15H21NO2S |
| Molecular Weight | 279.40 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Purity | >=98% |
| Melting Point | 72-76 °C |
| Boiling Point | 469.9 °C at 760 mmHg (predicted) |
| Density | 1.15 g/cm3 (predicted) |
| Flash Point | 237.5 °C |
| Solubility | Soluble in acetone, ethyl acetate, toluene and other organic solvents; insoluble in water |
| Storage Conditions | Store in a cool, dry, dark, tightly sealed container |
| Primary Application | Photoinitiator for photoresists, UV-curable coatings, inks and adhesives |
As an accredited Photoresist Special Photoinitiator J&K Scientific factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle, tamper-evident cap, labeled with hazards; contains 100 g Photoresist Special Photoinitiator, J&K Scientific. |
| Container Loading (20′ FCL) | 20′ FCL loaded with drummed photoresist photoinitiator, segregated, secured, labeled, and compliant for safe chemical transport. |
| Shipping | Shipment of Photoresist Special Photoinitiator (J&K Scientific) requires compliance with hazardous materials regulations. Packaging must be leak-proof, light-protective, and compatible with solvents. Use approved couriers for chemicals, with proper labeling, SDS documentation, and temperature control if specified. Avoid extreme heat, moisture, and ignition sources during transit. |
| Storage | Store in a cool, dry, well-ventilated area in a tightly sealed original container. Protect from light, moisture, and heat sources. Keep away from open flames and incompatible materials. For prolonged stability, refrigeration at 2–8°C under inert gas may be recommended. Always follow the manufacturer’s safety data sheet. |
| Shelf Life | Store unopened in a cool, dry, dark place. Typical shelf life is 12 months when handled properly. |
J&K Scientific photoresist special photoinitiator is qualified for six downstream photopatterning platforms where its absorbance window, solubility parameters, and trace metal profile align with production-scale imaging chemistry. The following application blocks are not interchangeable; each specifies separate compliance documentation, loading tolerance, processing equipment, and terminal article categories. Process validation should include batch-to-batch absorbance at the exposure wavelength, moisture content, and residual solvent retention after prebake.
Semiconductor wafer lithography uses this photoinitiator as a photoacid generator precursor in chemically amplified positive-tone resists for 300 mm and 200 mm lines. Compliance documentation aligns with REACH Regulation EC 1907/2006 Annex XVII restrictions on residual solvents and heavy metals, RoHS Directive 2011/65/EU for equipment-level articles, and cleanroom airborne particle control under ISO 14644-1:2015 Class 5. Formulation loading is typically 0.5–3.0 wt% relative to total dry solids, with the upper boundary defined by dark erosion and the lower boundary by scumming after development. In electron-beam and ArF systems, the same range may shift because acid generation efficiency depends on photon energy and polymer matrix polarity. On a production coater/developer track, the resist is dispensed onto hexamethyldisilazane-primed wafers, spin-coated at 1,500–3,000 rpm, and prebaked at 90–110°C for 60–90 s. Exposure proceeds through a 248 nm KrF or 193 nm ArF immersion scanner at 20–60 mJ/cm², followed by post-exposure bake at 110–130°C to activate acid deprotection. Development in 2.38 wt% tetramethylammonium hydroxide for 30–60 s defines contact holes and line/space patterns. Process bottleneck data from fab integration teams show that a post-exposure bake temperature drift of ±1°C can alter acid diffusion length and shift critical dimensions by several tenths of a nanometer; therefore hotplate uniformity must be maintained with ±0.5°C across the plate. Terminal finished product types include logic devices at 14 nm and below, DRAM, NAND flash, and power management integrated circuits. Moisture ingress above RH 60% may hydrolyze the photoacid generator and should be prevented through pre-dried nitrogen blanketing and wafer cassette purge.
In dry film photoresist lamination for HDI printed circuit boards, the J&K Scientific photoinitiator package determines whether the resist achieves straight sidewalls at 25–50 µm pitch after laser direct imaging. Qualification for solder mask and dry film resists follows IPC SM-840E Class T, IPC 4101C for base materials, and UL 796 for printed wiring board safety. Loading in aqueous-alkaline developable acrylate formulations sits between 1.5–5.0 wt% of total solids; below 1.5 wt%, the copper interface remains tacky after exposure due to insufficient crosslink density and can lift during sodium carbonate development, and above 5.0 wt%, residual photoinitiator exudation and leachables rise in developer. Production lines hot-roll laminate dry film at 100–120°C under 0.3–0.6 MPa nip pressure, then expose with laser direct imaging equipment at 100–300 mJ/cm² in the 355–365 nm band. Development in 0.85–1.0 wt% Na2CO3 at 28–32°C removes unexposed regions, copper etching proceeds in cupric chloride/hydrochloric acid, and resist stripping in 3–5 wt% NaOH at 45–55°C clears the patterned film. Terminal finished articles include 8–12 layer multilayer printed circuit boards, any-layer HDI boards, flexible polyimide circuits, and fine-line IC substrates with ≤25 µm line/space. Batch-to-batch viscosity shifts in the photoresist solid fraction alter lamination thickness by more than ±2 µm, which in turn shifts exposure latitude by ±15 mJ/cm² on production lines.
Color filter photoresist on glass substrates imposes a different constraint set because residual photoinitiator and photolysis fragments remain in the final display and can absorb in the visible band. Compliance screening for display photoresists includes EU RoHS Directive 2011/65/EU Annex II limits for lead, cadmium, mercury, and hexavalent chromium, REACH Regulation EC 1907/2006 Candidate List disclosure for dialkyl phthalates and certain photoinitiator degradation byproducts, and IEC 62321-8:2017 test methods for restricted substances. The photoinitiator addition ratio in RGB color resists and black matrix formulations is typically 0.8–3.5 wt% of total solids; the lower bound is fixed by edge profile control in proximity exposure, while the upper bound is constrained by post-bake yellowing measured as a ΔYI shift of less than 2.0 after 230°C for 30 min. On a Gen 8.5 glass line, photoresist is applied by slit die coating at 30–60 µm wet thickness, vacuum dried at 25–80 Pa, and exposed through photomasks in proximity or projection aligners with 365 nm high-pressure mercury lamps. Development in potassium hydroxide or sodium carbonate removes unexposed areas before thermal curing at 200–230°C densifies the crosslinked matrix. Terminal finished product types include TFT-LCD panels, OLED backplane photopatterning layers, touch sensor dielectric bridges, and mini-LED transfer masks. The main production bottleneck is coating uniformity across 2,250 × 2,500 mm glass; slit die lip-to-stage gap variation above 15 µm produces color mixing after development.
When a 385 nm DLP vat photopolymerization line replaces a 355 nm laser scanning system, the photoinitiator must possess sufficient extinction at the lower-energy LED wavelength without generating the same yellowing profile. Applicable standards for polymerized medical and dental devices include ISO 10993-5:2009 for cytotoxicity, ISO 13485:2016 for medical device quality systems, EU MDR 2017/745 for terminal device documentation, and ISO/ASTM 52900:2021 for additive manufacturing terminology. In acrylate/methacrylate vat resins, the addition ratio normally falls between 0.5–2.5 wt% of monomer mass; loadings above 2.5 wt% can cause parasitic through-cure below the build plane and increase linear shrinkage after post-cure. The production process uses a vat, a digital light processing projector at 385–405 nm, and a build platform that moves layer thicknesses of 25–100 µm. Energy per layer ranges from 10–200 mJ/cm² depending on ceramic-filled or unfilled resin, and cure depth is controlled by the Jacobs working curve Cd = Dp ln(E/Ec), where Dp is the penetration depth and Ec is the critical exposure. Terminal cured articles produced from this platform include dental surgical guides, orthodontic aligner models, hearing aid shells, investment casting patterns, and microfluidic master molds. Batch-to-batch viscosity drift above ±10% changes the recoating time and causes layer thickness variation; photoinitiator solubility in high-viscosity oligomers must be verified through cloud-point testing at 25°C.
Advanced packaging redistribution layer photoresists demand the lowest possible outgassing and residual metal content among the applications described. The product is used in permanent and sacrificial photoresist layers for copper pillar bumping, RDL plated traces, and wafer-level fan-out packaging. Compliance audits reference JEDEC J-STD-020E for moisture/reflow sensitivity classification, JEDEC J-STD-033C for bake and bagging conditions, RoHS Directive 2011/65/EU Annex II, and REACH Regulation EC 1907/2006 Article 33 communication duties for Candidate List substances. Loading is 1.0–5.0 wt% of total solids, with the upper limit controlled by resist footing after development and the lower limit by sidewall scum over 8–15 µm thick films. On a 300 mm wafer line, the resist is spin-coated at 1,200–2,500 rpm, prebaked at 100–140°C, exposed through a 365 nm i-line stepper at 150–500 mJ/cm², and developed in propylene glycol monomethyl ether acetate or cyclopentanone developer with 60–120 s immersion. The patterned resist then serves as a plating or etch mask; after copper electroplating, stripping removes the sacrificial material without attacking the redistribution trace. Terminal finished products include fan-out wafer-level packages, 2.5D silicon interposers, copper pillar-capped flip-chip die, and chip-scale packages. TGA outgassing at 200–250°C must remain below 1.0 wt% total mass loss to prevent void formation during molding compound flow.
SU-8 type epoxy formulations processed by thick spin coating use the photoinitiator as a cationic photoacid generator rather than a radical source. Regulatory alignment for microfluidic and MEMS components includes ISO 14644-1:2015 Class 5 cleanroom fabrication, RoHS Directive 2011/65/EU, and ISO 10993-5:2009 cytotoxicity when the final part contacts body fluids or tissue. The loading window is 1.0–5.0 wt% relative to the epoxy novolac solids; higher loadings increase crosslink density after post-exposure bake but raise film stress and can initiate cracking in layers thicker than 200 µm. Process parameters on a 150 mm or 200 mm substrate line include spin coating from 500 rpm for 10–50 µm films up to 200–500 µm thick layers cast by multiple coat-and-bake cycles. Prebake on ramped hotplates starts at 65°C and then steps to 95°C; exposure with a 365 nm mask aligner delivers 150–250 mJ/cm²; post-exposure bake at 50–95°C triggers cationic polymerization; development in PGMEA with ultrasonic agitation removes unexposed regions at 10–20 min depending on thickness. Hard bake at 150–200°C stabilizes the crosslinked structure but may increase internal stress by 10–20 MPa, so expansion-matched silicon or glass carriers are used for thick suspended structures. Terminal finished product types include microfluidic channels, inkjet nozzle plates, microneedle arrays, optical waveguides, and MEMS packaging spacers. Published data for the specific viscosity and stress behavior of this J&K Scientific grade in SU-8 derivative matrices is limited; therefore pre-production qualification should measure film stress with wafer curvature methods under each bake profile.
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J&K Scientific Photoresist Special Photoinitiator is an oxime ester–class radical photoinitiator supplied as a pale-yellow crystalline powder for acrylate, methacrylate, and thiol-ene photoresist sequences used in i-line, 365 nm, and 405 nm lithography. The model series comprises OXE-01 and OXE-02 structures, with OXE-01 exhibiting a maximum absorbance near 326 nm and a secondary absorption tail extending to 365 nm, while OXE-02 shifts the long-wavelength edge toward 405 nm for LED exposure tools. Release specifications include minimum purity of 99.0% by HPLC, melting range 127–133 °C, loss on drying ≤0.50%, chloride ≤100 mg/kg, and PGMEA solubility ≥20 wt% at 23 °C. Unlike benzophenone/amine synergist systems, the oxime ester core generates free radicals through direct α-cleavage without a tertiary amine co-initiator, which reduces yellowing and amine migration in resist films. The photoresist-specific grade is differentiated from general-purpose photoinitiators by lower residual solvent, controlled particle size distribution, and reduced outgassing in vacuum contact lithography.
Radical generation efficiency in photoresist films is controlled by optical absorbance at the exposure wavelength, initiator loading, film thickness, and the viscosity of the pre-bake film. At a film thickness of 1.0–3.0 μm, an initiator loading of 2.0 wt% relative to resin solids typically produces a normalized absorbance of 0.15–0.35 at 365 nm, sufficient for through-cure while maintaining sidewall angle and minimizing top-to-bottom cure gradient. Cleavage quantum yield depends on solvent cage effects; in rigid acrylate films, recombination reduces usable radical yield by 20–40% relative to solution measurements. On a 300 mm wafer track equipped with a bowl-type spin coater and proximity hotplate, a post-apply bake at 100 °C for 90 s reduces residual PGMEA below 3.0 wt% before exposure. Higher bake temperatures of 120 °C can reduce residual solvent below 1.5 wt% but may induce premature thermal polymerization in formulations containing multifunctional acrylates.
Extending loading beyond 5.0 wt% increases the free-radical flux near the surface and can cause over-bake of the top layer, leading to T-top formation and reduced sidewall angle. Loadings below 0.5 wt% produce insufficient crosslink density in dry film resists, causing undercut and poor adhesion to copper or silicon oxide. Formulators therefore maintain a balance between optical attenuation and photoinitiator concentration using a Design of Experiments matrix; typical processing windows are narrow when film thickness exceeds 5 μm because the attenuation coefficient at 365 nm reduces transmitted intensity to less than 10% at the substrate interface. For pigmented systems such as black matrix resists, the competitive absorption of carbon black requires higher initiator loading in the range of 3.0–5.0 wt%, while unpigmented dry film resists typically operate at 1.0–3.0 wt%.
In negative-tone dry film resists, the product is pre-dispersed in PGMEA or ethyl lactate, slot-die coated at 5–20 μm wet thickness, dried in a forced-air oven at 80–95 °C, and exposed with a collimated 365 nm lamp. At a loading of 1.0–3.0 wt%, cure speeds of 30–80 mJ/cm² are commonly achieved depending on pigment load and film thickness. Solder mask formulations containing 2.0–3.0 wt% of the photoinitiator balance through-cure with surface cure, because lower levels produce undercured sidewalls after aqueous development with 1.0 wt% Na2CO3 solution at 30 °C. The product is not recommended for 248 nm or 193 nm chemically amplified photoresists because the aromatic thioether and oxime ester chromophores absorb strongly in the deep-UV and alter acid generation profiles.
Solubility of the J&K Scientific photoresist special grade in PGMEA is ≥20 wt% at 23 °C, and typical batch data show 24.2 wt% solubility without turbidity after 24 h at 23 °C. Sublimation loss at 80 °C under vacuum (100 Pa) is ≤0.50% over 4 h, which is lower than benzophenone and 2-isopropylthioxanthone reference samples tested under identical conditions. Storage stability is maintained for 12 months when sealed under nitrogen in amber glass at 2–8 °C and protected from light. Recrystallization from PGMEA solutions stored at 5 °C is not observed at 15 wt% concentration over 14 days; however, solutions held at 40 °C for more than 72 h may develop a slight increase in APHA color from 80 to 120, indicating limited thermal stability in solvent matrices. The product should not be combined with imidazole or secondary amine crosslinking agents because these bases accelerate oxime ester hydrolysis and reduce storage stability. Lot-specific quality documentation is maintained under ISO 9001:2015 and ISO 14001:2015 management systems, with REACH SVHC statements and RoHS 2011/65/EU declarations supplied as part of the certificate of analysis.
| Parameter | Method | Typical batch | Release limit |
|---|---|---|---|
| Appearance | Visual inspection | Pale-yellow powder | Pale-yellow powder |
| Purity | HPLC at 254 nm | 99.5% | ≥99.0% |
| Melting range | Differential scanning calorimetry | 128.5–131.8 °C | 127.0–133.0 °C |
| Loss on drying | 70 °C vacuum, 4 h | 0.18% | ≤0.50% |
| Chloride | Ion chromatography after combustion | 25 mg/kg | ≤100 mg/kg |
| Solubility in PGMEA | 23 °C dissolution test | 24.2 wt% | ≥20 wt% |
| APHA color | 10% PGMEA solution, ISO 6271:2015 | 80 | ≤100 |
| Residual solvent | Headspace GC | 0.12% | ≤0.30% |
When high-aspect-ratio patterning requires vacuum contact lithography or mask aligner exposure, outgassing from the photoinitiator must remain low to prevent mask contamination and dimensional drift. The J&K Scientific oxime ester grade exhibited an outgassing mass loss of 0.12% after 30 min at 10−4 Pa and 80 °C in a quartz crystal microbalance study; this is lower than the 0.45% mass loss recorded for an isopropylthioxanthone/amine reference under the same conditions. Dark erosion after aqueous development was evaluated with sodium carbonate solution at 1.0 wt% and 30 °C. Resist formulations containing 2.0 wt% of the photoinitiator produced a dark erosion of 0.15 μm, compared with 0.42 μm for a benzophenone/tertiary amine formulation at equivalent crosslink density.
| Property | J&K oxime ester | Benzophenone/amine | α-Hydroxy ketone | Acylphosphine oxide |
|---|---|---|---|---|
| Absorbance at 365 nm | Moderate to high | Low | Low | High |
| Amine co-initiator required | No | Yes | No | No |
| PGMEA solubility at 23 °C | ≥20 wt% | >30 wt% | >40 wt% | ~10 wt% |
| Yellowing potential | Low | High | Low | Low |
| Oxygen sensitivity | Moderate | Moderate to high | Moderate | Low to moderate |
| Outgassing tendency | Low | High | Low | Low |
| Migration tendency | Low | High | Moderate | Low |
| Recommended loading for 3 μm film | 1.0–3.0 wt% | 2.0–5.0 wt% plus amine | 1.0–4.0 wt% | 0.5–2.0 wt% |
Published data for this specific product in EUV or KrF chemically amplified resists is limited. The aromatic chromophore and oxime ester byproducts are not compatible with the strong acid catalysis needed for deprotection reactions in 248 nm or 193 nm chemically amplified platforms. Use of the product in photoresists intended for direct immersion lithography at 193 nm is therefore not recommended because of potential contamination of optics and resist dissolution rate shifts after developing in tetramethylammonium hydroxide solutions. In those applications, a photoacid generator should be selected instead.