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Photoresist Thinner Electronic/EL Grade

    • Product Name: Photoresist Thinner Electronic/EL Grade
    • 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 732710
    Chemical Composition Mixture of organic solvents (e.g., propylene glycol monomethyl ether acetate, ethyl lactate, and butyl acetate)
    Purity 99.9% or higher (Electronic/EL Grade)
    Resistivity > 1 MΩ·cm
    Particle Count < 10 particles/mL (≥0.5 µm)
    Moisture Content < 100 ppm
    Metal Impurities < 1 ppb each (e.g., Na, Fe, Cu, Ni, Zn)
    Boiling Point 140–180 °C (depending on formulation)
    Flash Point 40–60 °C (closed cup)
    Density 0.85–0.95 g/cm³ at 20 °C
    Evaporation Rate 0.1–0.3 (butyl acetate = 1.0)
    Solubility Fully miscible with photoresist solvents and common organic solvents
    Acidity Or Alkalinity pH approximately neutral (6.5–7.5 in aqueous extract)

    As an accredited Photoresist Thinner Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 1-gallon high-purity HDPE bottle, Photoresist Thinner Electronic/EL Grade ensures safe solvent storage and dispensing.
    Container Loading (20′ FCL) 20′ FCL loaded with UN-approved drums of photoresist thinner, secured and segregated for safe transport.
    Shipping Photoresist Thinner Electronic/EL Grade ships as a flammable liquid (UN1993, Class 3, PG II) with proper labeling, grounding, and segregation from oxidizers. Pack in approved containers, secure against leakage, and avoid heat or ignition sources. Transport is available by ground, sea, or air under applicable dangerous goods regulations.
    Storage Store Photoresist Thinner Electronic/EL Grade in tightly sealed, original or compatible containers in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep between recommended temperatures (typically 15–25°C), separated from oxidizers, acids, and bases. Ground containers during transfer to prevent static discharge. Inspect periodically for leakage.
    Shelf Life Shelf life is typically 2 years from manufacture date when stored unopened in original container at room temperature.
    Application of Photoresist Thinner Electronic/EL Grade

    In front-end semiconductor manufacturing, the dilution of positive-tone novolac/diazonaphthoquinone (DNQ) photoresists is performed with electronic/EL-grade thinner to reduce dynamic viscosity before spin coating. The addition ratio is typically 5–30 wt% relative to photoresist mass, with 10–20 wt% being the prevailing window for i-line resists formulated for critical dimensions at or below 0.18 µm. At 23°C, the target spin-bowl viscosity is commonly 8–15 cP, measured on a Brookfield rotational viscometer with small-sample adapter. The solvent system is dispensed through point-of-use 0.05 µm membrane filtration and mixed inline to reduce bubble entrainment. On a coater/developer track, the same thinner is used undiluted in edge bead removal (EBR) nozzles placed 1–3 mm from the wafer perimeter, with backside rinse synchronized to the spin cycle. Quality conformance is specified under SEMI C30-0610 for photoresist thinner, with cleanroom handling controlled to ISO 14644-1 Class 5, trace metals by ICP-MS, and water by Karl Fischer titration per ASTM E1064-16. The downstream production flow comprises HMDS vapor priming, spin coating at 1500–4000 rpm, soft bake at 90–110°C, i-line/g-line exposure, post-exposure bake, and development in 2.38% TMAH. Terminal products include CMOS logic devices, DRAM and NAND memory die, microcontroller units, and power management ICs. Published data for film thickness variation below ±5 Å across high-vacuum track configurations is limited.

    What Limits Slit-Coater Throughput When Pigmented Photoresist Solids Are Reduced by Thinner Addition?

    Flat-panel display photoresists for color filter, black matrix, and photo spacer layers are supplied at high pigment loadings and require controlled dilution to match slit-coater rheology windows. The addition ratio for EL-grade thinner in red, green, and blue color filter resists is 10–40 wt%, with the upper boundary constrained by pigment dispersion stability and the onset of mottling after vacuum drying. Target cone-and-plate viscosity is 2.5–6.0 cP at 25°C, determined per ASTM D4287-19. The coating process operates on a slit coater with die-to-substrate gap of 100–250 µm and coating speed of 50–200 mm/s; after wet-film deposition, vacuum dry is maintained for 30–60 s, followed by prebake at 80–120°C, mask-aligned UV exposure at 100–300 mJ/cm², and development with TMAH or KOH-based developer. Conformance is anchored to REACH (EC) 1907/2006, RoHS Directive 2011/65/EU Annex II, and ISO 14644-1 Class 6 for cleanroom operation, with residual metals controlled under SEMI C30-0610. Terminal products include smartphone OLED panels, large-size LCD TV panels, notebook displays, and LC cell gap photo spacers. If thinner addition exceeds 40 wt%, the drop in viscosity tends to produce edge withdrawals and nonuniform color density across Gen 8.5 or larger substrates.

    Compliance reference matrix for application segments
    SegmentStandard/TestParameterTypical Limit
    Semiconductor front-endSEMI C30-0610; ASTM E1064-16Trace metals; water50 ppb total; ≤ 500 ppm
    Flat panel displayASTM D4287-19; RoHS 2011/65/EUCone/plate viscosity; restricted substances2.5–6.0 cP at 25°C; Annex II limits
    PCB/HDI solder maskIPC-SM-840E; UL 94 V-0Solder mask performance; flame classClass T/H; V-0
    Advanced packagingSEMI C30-0610; ISO 14644-1 Class 5Metals; airborne particles50 ppb each; ISO Class 5

    Liquid Photoimageable Solder Mask Thinning and Stencil Cleaning in HDI PCB Fabrication

    Liquid photoimageable solder mask (LPISM) formulations for high-density interconnect boards are adjusted with EL-grade thinner to lower screen-print viscosity without triggering pinhole formation. The formulation window for thinner addition is 5–20 wt%, bringing the ink to 40–80 dPa·s at 25°C when measured on a Brookfield viscometer with spindle #7 at 20 rpm. Above 20 wt%, the reduced solids content can compromise sidewall coverage on 30–75 µm copper features and increase the probability of pinholes after thermal cure. The downstream production sequence includes screen printing or curtain coating, pre-drying at 75–85°C for 15–30 min, UV or UV-LED exposure at 365 nm with 500–1000 mJ/cm², development in 1% Na₂CO₃ at 30°C, and final cure at 150°C for 60 min. The same thinner is used undiluted for cleaning of printing screens and stencil apertures after production stops, with waste handling under REACH (EC) 1907/2006. Qualification of solder mask performance follows IPC-SM-840E, with flame class verified to UL 94 V-0. Terminal products include HDI smartphone motherboards, IC substrates for ball grid array packages, and automotive electronic control unit boards exposed to thermal cycling from −40°C to +125°C.

    When Spin-Curve Uniformity in Wafer-Level Packaging Depends on Thinner Evaporation Rate

    At spin-coat stations for wafer-level packaging, high-solids photoresists used in bumping and redistribution layer (RDL) processing are thinned to suppress radial striations and control edge bead height. The addition ratio is 10–30 wt%, with target post-soft-bake film thickness of 5–50 µm. In this application, the evaporation rate differential between PGMEA and ethyl lactate in the thinner directly affects edge bead formation and thickness uniformity; slower-venting blends reduce radial nonuniformity to below ±3% across 300 mm wafers in a closed-bowl spin coater. The process sequence includes spin coating at 800–2500 rpm, soft bake at 110–130°C, i-line exposure at 365 nm, post-exposure bake, development with 2.38% TMAH, and subsequent electroplating of Cu/Ni/SnAg pillars or bumps. Conformance to SEMI C30-0610 applies for trace metal control, while floor operation is maintained to ISO 14644-1 Class 5, with individual metal content held at ≤ 50 ppb by ICP-MS. Terminal products include fan-out wafer-level packages, flip-chip bumps, copper pillar interconnects, and RDL layers for heterogeneous integration. The thinner should not be combined with solvent-sensitive temporary bonding adhesives unless compatibility has been verified on the specific carrier system.

    Across MEMS and image sensor fabs using thick positive-tone photoresists, thinning is limited to 0–15 wt% because excess solvent reduces film thickness and extends soft-bake time. At 10–15 wt% addition, a single-coat thickness of 20–100 µm is achievable at spin speeds of 500–2500 rpm; multi-layer coating at 100–150 µm requires staged hotplate baking at 65–95°C to prevent solvent pop defects. The thinner is dispensed through 0.1 µm point-of-use filters to protect deep reactive-ion etching masks and to avoid particle transfer into high-aspect-ratio trench structures. The production flow includes spin coating, direct alignment exposure on a contact aligner or i-line stepper, post-exposure bake, and development with PGMEA-based developer for 3–10 min using immersion or spray modules. Compliance is maintained under SEMI C30-0610, ISO 9001:2015, and RoHS 2011/65/EU for packaged sensor devices. Terminal products include MEMS inertial measurement units, microfluidic lab-on-chip cartridges, CCD/CMOS image sensors, and silicon microphones. Published data for the effect of thinner addition on high-aspect-ratio mold release performance is limited.

    Photomask Blank Cleaning and Pre-Coating Solvent Conditioning Requirements

    In photomask blank manufacturing and patterning, EL-grade thinner is used undiluted for edge bead removal and final solvent rinse, while the dilution ratio for electron-beam or 193-nm photoresists is 0–5 wt%. The cleaning sequence begins with quartz or attenuated phase-shift blank cleaning, followed by final solvent rinse and spin dry at 1500–2500 rpm on a mask cleaner/spin processor. Because haze defects can originate from residual solvent, the thinner must meet stringent moisture and particle specifications; water content is controlled by Karl Fischer titration per ASTM E1064-16, and particle counts above 0.1 µm are monitored by laser particle counter. Cleanroom conditions follow ISO 14644-1 Class 4, and chemical quality is referenced to SEMI C30-0610. The downstream process includes HMDS vapor priming, spin coating at 1000–3000 rpm, e-beam or laser exposure, development, chrome etch, resist strip with O₂ plasma, and final solvent cleaning. Terminal products include 193-nm binary masks, attenuated phase-shift masks, and phase-shift test reticles. Published data for EL-grade thinner as a final rinse on EUV mask blanks is limited and requires separate validation for tin migration risk.

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    Certification & Compliance
    More Introduction

    Photoresist Thinner Electronic/EL Grade is a controlled-purity solvent blend intended for dilution of positive-tone and negative-tone photoresist formulations and for edge-bead removal on wafer-coating equipment. A representative supplier model designation is PRT-EL-200, with EL indicating electronic-grade certification; exact model suffixes are supplier-specific and typically denote base-solvent composition, packaging, or filtration class. The product is based on propylene glycol monomethyl ether acetate (CAS 108-65-6), ethyl lactate (CAS 97-64-3), n-butyl acetate (CAS 123-86-4), or defined mixtures of these solvents. Each lot is filtered through 0.05 µm or 0.1 µm fluoropolymer membranes, packaged in pre-cleaned stainless steel or high-density polyethylene containers, and blanketed with nitrogen to limit moisture uptake to 0.05 wt% or less. The formulation differs from technical-grade and reagent-grade thinners by reducing alkali metal, transition metal, chloride, sulfate, and particle burdens to levels compatible with 248 nm and 193 nm photoresist processes, where ionic contamination alters photospeed, dark erosion, and residue formation.

    Representative release criteria for a PGMEA-based EL-grade thinner are listed in Table 1; supplier-specific limits may be tighter for sub-10 nm node lithography. The certificate of analysis for each lot normally reports the test method designation alongside the release value, and the user of record must verify that the method aligns with the fab chemical specification. For ethyl lactate-containing blends, the water limit is often tightened to 0.03 wt% because ethyl lactate hydrolyzes to lactic acid and ethanol, shifting acidity and decreasing dark erosion stability in chemically amplified resists.

    PropertyTest methodRelease limitUnit
    Density at 20 °CASTM D40520.968–0.972g/cm³
    WaterASTM D13640.05wt%
    ColorASTM D120910Pt-Co
    Acidity as acetic acidASTM D16130.01wt%
    Nonvolatile residueASTM D13535mg/L
    Flash point, PGMEA-rich blendASTM D327842–46°C
    Particles ≥ 0.5 µmLaser particle counter20particles/mL
    Metals, Na, K, Fe, CrDirect-injection ICP-MS; NIST SRM 1640a calibration20 per elementµg/kg

    Filtration cartridges used for EL-grade thinner are typically hydrophobic PTFE membranes with polypropylene supports and 316L stainless steel housings. Dispense pumps must be fitted with PTFE or perfluoroelastomer seals because PGMEA can cause nitrile O-ring swell greater than 15%, producing particle shedding and backstream contamination. Field data from coater/developer track installations show that a leaking O-ring on a 0.5 L/min chemical pump can raise particle counts at ≥ 0.5 µm from 10 particles/mL to more than 200 particles/mL within 24 h.

    How Do EL-Grade and Technical-Grade Thinners Differ in Particle and Metal Burdens?

    Three solvent grades are commonly confused: EL-grade, technical-grade, and ACS reagent-grade. The table below compares representative commercial ranges reported in supplier certificates of analysis; individual lots vary with feedstock and purification route. The operational difference is not assay alone, because a reagent-grade solvent may have high GC purity but uncontrolled sub-µm particle counts and mobile-ion contaminants that are irrelevant to analytical chemistry but destructive in photolithography.

    ParameterEL GradeTechnical-grade thinnerReagent-grade solvent
    Assay99.5%98.0%99.0% ACS
    Water0.05 wt%0.1–0.5 wt%0.1 wt%, supplier-dependent
    Total alkali and transition metals50 µg/kg1–10 mg/kg1 mg/kg typical
    Chloride and sulfate0.05 mg/kg each1–10 mg/kg1 mg/kg
    Particles ≥ 0.5 µm20 particles/mL> 1000 particles/mLNot controlled
    Filtration0.05–0.1 µm membrane0.45–1 µm membraneNot specified
    Application248 nm and 193 nm lithographyIndustrial coating thinningLaboratory and analytical use

    Sodium and potassium are mobile-ion sources; concentrations above 1 × 1011 atoms/cm² produce C-V hysteresis in gate oxide reliability testing on mercury-probe C-V analyzers. Iron and chromium reduce minority carrier lifetime and can form surface residues after plasma etch, shifting via contact resistance above 5% on 130 nm and smaller line dimensions. Chloride and sulfate are not innocuous at trace levels because they accelerate local corrosion of aluminum pads and copper interconnects during solvent evaporation on heated process surfaces.

    Process Usage: Viscosity Dilution, Edge Bead Removal, and Coater Bowl Rinsing

    For viscosity adjustment, the thinner is metered into the photoresist under recirculation in a chemical dispense system. The addition is calculated gravimetrically because density differences between PGMEA (0.970 g/cm³ at 20 °C) and photoresist solids affect volumetric dosing. A 5 wt% addition to a 15 cP i-line resist can reduce dispense viscosity to 10–12 cP at 25 °C when measured by ASTM D445 or a cone-and-plate rheometer at 10 s⁻¹; the exact reduction depends on solids content and polymer molecular weight. The thinner is not a universal diluent for all resin systems because high molecular weight novolac resists may phase-separate when n-butyl acetate exceeds 30 wt% of the solvent blend, producing hazy films and gel particles.

    Over-dilution beyond 10 wt% shifts film thickness below the swing-curve minimum on 200 mm and 300 mm wafers, increasing pinning defects at the wafer edge. The resulting thickness loss is visible on ellipsometer maps as a radial gradient, with center-to-edge variation exceeding 3 nm when the spinning program is not re-optimized. Batch-to-batch variance in thinner density of ±0.002 g/cm³ is sufficient to alter gravimetric dispensing by 0.2 wt% on a 400 L/day dispense loop; therefore, density verification per ASTM D4052 is required before connecting a new drum to the track chemical management system.

    Edge-bead removal uses a dedicated EBR nozzle on a coater/developer track. Typical dispense volumes are 0.5–2.0 mL per wafer for a 200 mm substrate, with spin speeds of 800–1500 rpm and dispense time 0.5–1.5 s. The solvent dissolves the thick resist bulge at the edge, preventing flake redeposition during exposure or hotplate baking. Nozzle arm height and radial position require tight adjustment; the radial position is usually 2–3 mm from the wafer edge, and backside rinse overlap of 2 mm prevents bead lifting at the wafer bevel. A misaligned EBR nozzle can leave a residual bead height greater than 10 µm, which flakes during softbake and creates coating defects on adjacent wafers.

    Coater bowl rinsing and nozzle purge cycles use spray or condensed vapor delivery. The product leaves no surfactant residue; this is a key difference from formulated edge-bead removers that contain cyclohexanone/acrylate wetting agents and can alter photoresist surface free energy. For negative-tone resists, residual thinner in the coater bowl must be exhausted at face velocity greater than 0.5 m/s to prevent solvent wandering and thickness nonuniformity in the central die area.

    For EUV photoresist dilution, published data for this specific configuration is limited; qualification on a track coater with inline particle monitoring and post-develop residue inspection is required before release for sub-7 nm node processes. The lower vapor pressure of some EL-grade blends can change the drying gradient during spin coating, so softbake hotplate uniformity must be verified against ±0.5 °C across the plate surface.

    When Storage Water Uptake Shifts the Dilution Curve Beyond Process Tolerances

    Moisture ingress is the primary storage failure mode. PGMEA and ethyl lactate absorb atmospheric water; a container opened in a 60% RH cleanroom can show water content increase from 0.02 wt% to 0.08 wt% within 48 h when measured by ASTM D1364. Water hydrolyzes ethyl lactate to lactic acid and ethanol; lactic acid increases titratable acidity above 0.01 wt% and can neutralize photoacid generators in chemically amplified 193 nm resists. The resulting exposure dose drift is observed as CD shift greater than 2 nm per 0.01 wt% water for a representative 90 nm line/space process.

    The hydrolysis equilibrium is temperature-dependent, and stationary storage temperatures above 25 °C accelerate acid formation. Containers should be kept under 0.05 µm-filtered nitrogen headspace at 20–40 L/min during dispense, and point-of-use filters must be hydrophobic because water-wet membranes slug and release droplets during initial dispense. Do not use compressed air for headspace blanketing; the oil mist and water content of standard plant air exceed 0.1 µm particle and 50 mg/m³ water ingress limits and will contaminate the thinner within a single drum-emptying cycle.

    Storage in 316L stainless steel containers is preferred over mild steel because iron pickup can exceed 1 mg/kg after 30 days in unlined carbon steel. Fluoropolymer-lined containers are acceptable when the liner is tested for extraction under 40 °C accelerated storage and shows no nonvolatile residue increase above 5 mg/L by ASTM D1353.

    Before specifying this thinner for a non-semiconductor photoresist process, the responsible process engineer must verify compatibility with the photoresist photoacid generator and polymer resin. The product should not be combined with amine-based additives, ammonia-containing cleanroom chemicals, or strong oxidizers. Amine contamination at 10 ppb can shift photospeed in chemically amplified resists because amines act as acid quenchers. This product is not a formulated developer or stripper; it is not intended for wafer descum, post-etch residue removal, or lift-off processing. For coater/developer tracks with non-CPVC fluid lines, the solubility parameter difference between PGMEA and n-butyl acetate blends requires elastomer swell verification against SEMI F57 or equivalent chemical compatibility data before installation.

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