| HS Code | 486768 |
| Product Name | Acidic Stripper Electronic/EL Grade |
| Grade | Electronic/EL |
| Appearance | Clear liquid |
| Color | Colorless to light yellow |
| Odor | Pungent acidic odor |
| Ph | Less than 2 |
| Specific Gravity | 1.1 - 1.3 at 20°C |
| Boiling Point | Above 100°C |
| Solubility In Water | Miscible |
| Etch Stripping Selectivity | Effective on photoresist and organic residues without attacking underlying metal layers |
As an accredited Acidic Stripper Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in a 1-gallon high-purity container, Acidic Stripper Electronic/EL Grade ensures safe handling for precision semiconductor and electronic cleaning applications. |
| Container Loading (20′ FCL) | 20′ FCL, secure drums/carboys of acidic electronic-grade stripper, segregated, labeled, with absorbents and proper ventilation for safe transit. |
| Shipping | Acidic Stripper Electronic/EL Grade requires corrosion-resistant, sealed containers with acid-proof labeling. Ship as hazardous material (Class 8), using UN-approved packaging and grounded vehicles. Segregate from bases and oxidizers. Ensure secondary containment to prevent leaks. Maintain temperature stability, avoid moisture, and provide clear handling documentation for safe transport. |
| Storage | Store in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong bases or reactive metals. Keep the original container tightly sealed when not in use. Ensure secondary containment and spill controls are available. Use corrosion-resistant shelving and follow all local regulations for hazardous chemical storage. |
| Shelf Life | Shelf life is typically 12 months when stored unopened in original containers at recommended temperatures, away from light and moisture. |
Acidic stripper electronic/EL grade is applied across advanced packaging, printed circuit board, display, and compound semiconductor manufacturing where low metal impurity and controlled corrosion rates are required for resist and residue removal. Lot-release analytical control for the undiluted product includes ICP-MS per ASTM D5673-16 for sodium, potassium, iron, copper, calcium, and zinc at ≤10 ppb each, ion chromatography per ASTM D4327-17 for chloride at ≤200 ppb, and particle counting at 0.2 µm with ≤10 particles/mL at point of fill. The product is filtered through 0.1 µm PTFE media and is supplied with a kinematic viscosity below 5 mm²/s at 25 °C for steady metering in short-loop recirculation systems. The following application scenarios are separated by process type and downstream terminal device class; they are not interchangeable with alkaline or solvent-only stripper chemistries.
Semiconductor wafer bumping and redistribution-layer photoresist stripping in 300 mm copper pillar processing begins with positive-tone novolak resist shells of 8–12 µm thickness patterned over Ti/Cu seed layers and electroplated with copper pillar and tin-silver cap structures. After plating, the resist shell is removed in a single-wafer spray processor with PTFE/PFA wetted parts. The acidic stripper concentrate is metered into 18 MΩ·cm deionized water at a 1:3 volumetric ratio, producing a nominal 25 vol% active bath. Bath temperature is maintained at 55–65 °C; spray nozzles deliver 1.2–1.8 L/min per nozzle with wafer rotation from 300 rpm to 800 rpm, and contact time is 90–150 s depending on resist cross-link density. The post-strip rinse uses 18 MΩ·cm deionized water at 25 °C until final surface conductivity is below 0.5 µS/cm. The critical production limit for this process is copper etch rate, which is held at 0.3–0.8 Å/s on patterned copper coupons; above 1.0 Å/s undercut appears on 25 µm pitch copper pillar structures. Chamber exhaust is maintained at −50 Pa differential to control acid aerosol drift, and all wetted surfaces are PTFE or PFA because 316L stainless steel shows intergranular attack above 60 °C in this acidic service. Recirculation filtration uses 0.1 µm PTFE cartridges, and dissolved metal cations are removed by cation-exchange columns regenerated with 10 wt% methanesulfonic acid. Analytical compliance is performed by ICP-MS per ASTM D5673-16 for trace metal cations and by ion chromatography per ASTM D4327-17 for chloride and sulfate; RoHS Directive 2011/65/EU Article 4(1) restrictions on lead, cadmium, mercury, and hexavalent chromium apply to the packaged device after strip. Terminal product types are copper pillar bumped wafers, redistribution layers, flip-chip chip-scale packages, and wafer-level packaged processors used in mobile and high-performance computing modules.
Horizontal conveyorized spray chambers processing 0.4–0.8 mm core substrates for semi-additive HDI microvia fill present a bath-life limitation that is more dependent on metal loading than on acid depletion. Concentrated acidic stripper is proportioned into the first sump at 10–12 vol% and into the second cascade at 5–8 vol%; the operating window is 45–55 °C at top and bottom spray manifold pressure of 1.8–2.5 bar. Conveyor speed is set between 1.2 m/min and 1.8 m/min for 15–25 µm dry film; peel completion is verified by backlight inspection and IPC-A-600H Class 2/3 acceptance criteria for lifted or residue-retained traces. When cupric ion loading exceeds 2,000 mg/L and total dissolved solids exceed 35 g/L, re-deposited polymer fragments adhere to copper traces and strip time increases from 45 s to more than 110 s on the same panel configuration. Production lines slow the failure by bleed-and-feed at 8–12 L/min per chamber, with dissolved copper removed by ion-exchange or electrowinning side loop. Chamber sump screens are 100 mesh PTFE-coated filters cleaned every 2 h; failure to remove dry film flakes raises strip time and deposits residue onto final rinse rollers. Automated titration maintains acid concentration within ±0.3 vol%; in-line pH is held between 2.8 and 3.4. Final cascade rinse water is held below 10 µS/cm conductivity at 25–35 °C, followed by heated air-knife drying. Compliance standards for this line include IPC-TM-650 Method 2.3.25C for ionic cleanliness using resistivity of solvent extract, IPC-6012E Section 3.8 for surface contamination limits with ≤1.56 µg/cm² NaCl equivalence maximum, and RoHS Directive 2011/65/EU Annex II for lead-free compatibility of the stripped panel surface. Terminal product types include HDI smartphone mainboards, package substrates for chip-scale packages, SSD carrier boards, and automotive ADAS rigid-flex multilayer circuits.
| Downstream segment | Test method / standard | Control limit | Verification point |
|---|---|---|---|
| 300 mm wafer bumping / RDL | ASTM D5673-16 ICP-MS | ≤10 ppb total Na, K, Fe, Cu, Ca, Zn in undiluted product | incoming lot release and bath make-up |
| HDI PCB dry film stripping | IPC-TM-650 Method 2.3.25C; IPC-6012E Section 3.8 | ≤1.56 µg/cm² NaCl equivalence after final rinse | post-strip panel coupon |
| Gen 8.5 TFT array | SEMI Grade 5 cation criteria; ASTM D4327-17 | ≤10 ppb individual cations; ≤200 ppb chloride | bulk supply and recirculation loop |
| LED pattern plating lift-off | ASTM D5673-16; ASTM D512-23 | ≤10 ppb trace metals; ≤200 ppb chloride | bath after cation exchange |
| SAW/BAW IDT lift-off | SEMI Grade 5; ASTM D5673-16 | ≤200 ppb Fe and Cu in bath | every 4 h during batch operation |
| WLCSP UBM residue removal | ASTM D3359-23 cross-hatch; ASTM D5673-16 | polyimide adhesion ≥4B; trace cations ≤10 ppb | post-process monitor wafer |
Flat panel display TFT array photoresist stripping after wet etch on Gen 8.5 lines uses an in-line spray processing module. The source-drain electrode stack is typically Mo/Al/Mo, wet-etched with phosphoric-nitric-acetic acid mixtures before residue removal. The acidic stripper is injected at 15 vol% into an in-line spray processing module with 85 vol% ultrapure water at 40–50 °C; a chelating agent package is maintained at 0.4–0.7 wt% to complex aluminum and molybdenum ions and prevent aluminum hydroxide precipitation on panel edges. Contact time through the spray chamber is 75–120 s for 1.0–1.5 µm residual photoresist after dry etching; line speed is set to the chamber length to maintain the required exposure. After stripping, two-stage deionized water rinsing at 18 MΩ·cm continues until molybdenum residue on monitor wafers is below 1×1010 atoms/cm² by total reflection X-ray fluorescence. The recirculation loop is monitored by particle counters; the bath is exchanged when particle counts exceed 50 particles/mL at 0.3 µm size. Compliance includes SEMI Grade 5 metallic cation specifications, anion confirmation by ASTM D4327-17 ion chromatography, and REACH Regulation (EC) No 1907/2006 Article 33 communication for SVHC content above 0.1 wt%. Terminal product types are Gen 8.5 thin-film transistor arrays for 4K and 8K LCD televisions, desktop monitors, notebook panels, and automotive dashboard displays.
On sapphire and GaAs LED front-end lines, a positive-tone photoresist mold of 6–10 µm thickness defines Ni/Au or Ni/Cu/Au bond pads and current-spreading fingers. After electroplating, the resist mold is removed in a quartz immersion tank with megasonic agitation at 40 kHz and power density 2 W/cm². The concentrated stripper is charged at 12–18 vol% in deionized water; bath temperature is held at 50–60 °C, and pH is maintained between 2.5 and 3.5. Strip time ranges from 180 s to 360 s for the upper end of the thickness range; endpoint is determined by dark-field optical inspection and water contact-angle hysteresis below 10° on monitor coupons. The main production limit is zinc and copper cross-contamination from electroplating drag-in; when zinc exceeds 500 ppb in the working bath, lift-off surfaces show re-deposited metal oxide specks. The bath is therefore recirculated through 0.05 µm PTFE filters, and cation-exchange columns are used for trace metal extraction. Incoming product analytical compliance uses ICP-MS per ASTM D5673-16 for sodium, potassium, iron, copper, calcium, and zinc at ≤10 ppb each, chloride by ASTM D512-23 at ≤200 ppb, and RoHS Directive 2011/65/EU Annex II restrictions on lead, mercury, cadmium, and hexavalent chromium in final LED terminals. Terminal product types include red, green, blue, and ultraviolet LED chips in surface-mount packages, infrared emitters, and automotive-grade high-brightness LED arrays.
| Segment | Bath dilution / addition ratio | Temperature | Contact time | Primary endpoint / limiting condition |
|---|---|---|---|---|
| 300 mm wafer bumping / RDL | 1:3 concentrate / DI water (25 vol%) | 55–65 °C | 90–150 s | Cu etch rate ≤0.8 Å/s |
| HDI PCB dry film stripping | 10–12 vol% first sump; 5–8 vol% second cascade | 45–55 °C | 45–110 s | Cu²⁺ ≤2,000 mg/L; TDS ≤35 g/L |
| Gen 8.5 TFT array | 15 vol% concentrate | 40–50 °C | 75–120 s | Mo residue ≤1×1010 atoms/cm² |
| LED pattern plating lift-off | 12–18 vol% concentration | 50–60 °C | 180–360 s | Zn ≤500 ppb in bath |
| SAW/BAW IDT lift-off | 1:5 concentrate / DI water (16.7 vol%) | 65–70 °C | 20–40 min | open-circuit Al −0.85 V to −0.65 V vs Ag/AgCl |
| WLCSP UBM residue removal | 1:4 concentrate / DI water (20 vol%) | 60 °C | 180 s | polyimide cross-hatch adhesion ≥4B per ASTM D3359-23 |
Acoustic filter lift-off on lithium tantalate or lithium niobate wafers uses image-reversal photoresist to define interdigital transducer electrode patterns, typically 0.2–0.5 µm line/space. After electron-beam evaporation of Al or Al/Cu/Al metal stacks, unwanted metal is removed by lift-off in an acidic stripper bath. The material is diluted 1:5 with 18 MΩ·cm deionized water and heated to 65–70 °C in a quartz recirculation vessel; the bath is agitated by nitrogen bubbling at 20–40 L/min per batch. Immersion time is 20–40 min for 1.0–1.2 µm resist, with lift-off completion confirmed by automated optical inspection and scanning electron microscopy. The 16.7 vol% concentrate addition is selected to avoid aluminum attack; open-circuit potential of the aluminum IDT is monitored and held between −0.85 V and −0.65 V versus Ag/AgCl reference. Bath chemistry is checked by inductively coupled plasma mass spectrometry every 4 h; iron and copper must remain below 200 ppb to prevent galvanic pitting on the IDT metal. Compliance standards include SEMI Grade 5 metallic cation limits, ASTM D5673-16 for trace metals, and RoHS Directive 2011/65/EU Article 4(1) restrictions for final packaged devices. Terminal product types are surface-acoustic-wave and bulk-acoustic-wave filters for 5G RF front-end modules, Wi-Fi 6E/7 radio modules, and automotive vehicle-to-everything communication filters.
When an acidic stripper replaces organic amine ash residue removers in wafer-level chip-scale packaging, the primary trade-off is copper-compatible residue removal without delaminating polyimide passivation. The material is metered into a single-wafer spin processor at 1:4 dilution, yielding 20 vol% concentration and 60 °C process temperature. Dispense flow is 0.8–1.2 L/min through a low-shear nozzle; wafer rotation is staged at 300 rpm during chemical puddle and 1,200 rpm during rinse. Contact time is 180 s for post-plating residue removal from 30 µm pitch Cu/Ni/Au under-bump metallization pads. Process limits are set by polyimide adhesion: a cross-hatch adhesion test per ASTM D3359-23 is performed on the passivation edge after processing, and any rating below 4B triggers immediate bath renewal. The formulation addition ratio must not exceed 25 vol% because above that threshold polyimide surface roughness increases above 5 nm Ra, measured by atomic force microscopy on monitor wafers. Analytical controls include ICP-MS per ASTM D5673-16 for metal cations, ion chromatography per ASTM D4327-17 for anions, and RoHS Directive 2011/65/EU Annex II restrictions for lead and cadmium in the final wafer. Terminal products include WLCSP devices for power management ICs, MEMS microphones, ambient light sensors, and wearable health monitoring chips.
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Acidic Stripper Electronic/EL Grade is supplied as a low-metal, low-particle aqueous acidic photoresist stripping formulation for wet-bench and single-wafer spray processing. The Electronic/EL designation functions as a specification code rather than a fixed molecular identity; the product is controlled by trace metal ceilings, submicron particle counts, final filtration state, and packaging cleanliness. The as-received material is a clear to pale-yellow liquid with a density at 20°C of 1.18–1.25 g/cm³ determined by ASTM D4052. Active acidity is reported as sulfuric acid and is typically held at 25.0–35.0 wt% by potentiometric titration. A 1% aqueous dilution exhibits a pH below 2.0; pH is not used as a primary release criterion because strong acid titration provides better repeatability. The product is an oxidizing acid system, and storage requires vented high-density polyethylene or fluoropolymer containers to manage oxygen evolution from peroxide decomposition. Lot-specific certificates of analysis define the actual shipped values; the grade name is not an assay value and should not be used to prepare process dilutions without consulting the lot-specific density and active-acid concentration.
Electronic-grade release is distinguished from technical acidic strippers principally by the sum of critical cation contamination and the submicron particle burden. Trace metal analysis is performed by inductively coupled plasma mass spectrometry using EPA Method 200.8 or an equivalent laboratory procedure validated to a detection limit below 0.5 µg/kg. Iron, chromium, nickel, copper, and zinc are controlled to individual concentrations not exceeding 10 µg/kg; sodium, potassium, calcium, and magnesium are controlled to 5 µg/kg or lower when frontside wafer contact is planned. Total cation contamination is held below 50 µg/kg. Particulate matter at the ≥0.5 µm channel is measured with a laser particle counter qualified to ISO 21501-4, with a release limit of 25 counts/mL. Anionic impurities are quantified by ion chromatography per ASTM D4327, with chloride below 0.5 mg/kg and nitrate below 1.0 mg/kg for front-end use. Sulfate is not counted as an impurity because sulfate is the intended counterion from sulfuric acid. The table below lists the typical release criteria.
| Parameter | Method or standard | Limit |
|---|---|---|
| Active acidity as H₂SO₄ | Potentiometric titration | 25.0–35.0 wt% |
| Density at 20°C | ASTM D4052 | 1.18–1.25 g/cm³ |
| Particles ≥0.5 µm | ISO 21501-4 | ≤25 counts/mL |
| Fe, Cr, Ni, Cu, Zn | EPA 200.8 ICP-MS | ≤10 µg/kg each |
| Na, K, Ca, Mg | EPA 200.8 ICP-MS | ≤5 µg/kg each |
| Total trace metals | EPA 200.8 ICP-MS | ≤50 µg/kg |
| Chloride | ASTM D4327 | ≤0.5 mg/kg |
| Nitrate | ASTM D4327 | ≤1.0 mg/kg |
Process data from immersion wet benches with 40–60 L PFA or PTFE tanks indicate that effective photoresist removal occurs at a bath temperature of 70–80°C for positive-tone novolak/diazonaphthoquinone films of 1.5–2.0 µm thickness. The wetted path in these tools includes quartz immersion heaters and 0.1 µm PTFE recirculation filters; continuous filtration is required to reduce particle re-deposition as resist films dissolve. At 70–80°C, static immersion clearing times are 8–15 minutes; with 950 kHz megasonic agitation through a quartz transducer plate, clearing time decreases to 4–7 minutes for the same film thickness. The bath is controlled by oxidation-reduction potential rather than by visual color, because dissolved resist carbon darkens the solution without indicating loss of active oxygen. In high-volume production, dissolved aluminum from previous substrate contact has been observed to reduce stripping rate and increase frontside metal contamination when the concentration exceeds 15 mg/L; a cation-loaded bleed-and-feed or partial bath replacement is used to hold aluminum below this threshold. The product is not recommended for extended immersion of unprotected copper at the upper end of the temperature range because acidic peroxide chemistry etches copper at a finite rate. For exposed aluminum pads, the processing temperature should not exceed 80°C, and the peroxide concentration must remain within the supplier’s shipping specification. Localized pad attack occurs when the bath is over-oxidized or when dissolved metal concentrations are allowed to rise. The critical process boundary is therefore not active-acid assay alone but the combination of temperature, redox potential, and dissolved metal burden.
Single-wafer spray processing changes the control problem from bath metal accumulation to puddle control, dispense stability, and final-fill particle cleanliness. In a single-wafer processor with a 0.6–1.2 L/min flow and a 22 MHz megasonic nozzle, the product removes the same photoresist film in 60–150 seconds at a platen temperature of 65–75°C. Because the chemical is not recirculated through a bath, trace metal buildup is lower than in immersion, but the wafer sees fresh chemical, and therefore the particle cleanliness of the final fill is critical. Nozzle clogging is a known failure mode when the product is used with older stainless steel lines; fluoropolymer or quartz fluid paths are required to avoid iron pickup. Spray processing consumes more volume per wafer than immersion, and waste neutralization must account for both residual peroxide and low pH. Oxidation-reduction potential in spray mode is less diagnostic than in immersion because residence time is short; dispense pressure, flow stability, and exhaust flow are more relevant for uniform stripping. Process engineers typically monitor strip uniformity with a 49-point film-thickness map after stripping and a dark-field particle scan before and after processing.
Qualification for replacement of a solvent-based or semi-aqueous photoresist stripper with the acidic electronic/EL grade must address rinsewater compatibility, exhaust handling, and substrate metallization. The formulation is water-rinsable after a 2–5 minute overflow rinse at 20–40°C, eliminating the intermediate solvent rinse step that semi-aqueous products require. In back-end bumping and redistribution-layer flows, the product is considered when plasma-ashed residues contain metal oxide or silicon-containing debris that neutral solvent systems do not disperse. The principal comparative advantage is the lower trace metal loading across the wafer environment; the EL-grade ICP-MS ceiling prevents uncontrolled sodium and iron addition from packaging and transfer lines. However, the product is not a drop-in neutral replacement: its acidic pH can mobilize aluminum and copper from unprotected pads, and corrosion qualification must use the exact metallization stack. A corrosion coupon study with a post-clean scanning electron microscope review at 10,000× is used to check pitting or undercut. The chloride ceiling of 0.5 mg/kg reduces copper pitting risk relative to technical acid strippers with higher halide background, but it does not eliminate the need for electrochemical compatibility testing. For copper/low-k integration, process qualification should include contact angle shift, k-value restoration, and leakage current measurement after the full wet sequence. Published comparative data for specific low-k dielectrics is limited; these measurements should therefore be obtained on the actual device stack.
Compared with general industrial acidic stripper concentrates, the electronic/EL grade is separated by final filtration, cleanroom container preparation, and analytical release. The product is filled in a cleanroom through 0.1 µm or smaller rated membrane filters that are integrity-tested before and after filling. Bulk containers are nitrogen-blanketed high-density polyethylene drums or fluoropolymer totes pre-rinsed with 18.2 MΩ·cm deionized water. Industrial grades may be sold without final filtration and can carry particulate loads above 100 counts/mL at the ≥0.5 µm channel. For low-density printed circuit board resist stripping, a technical acid stripper may be sufficient; for wafer-level, MEMS, or advanced packaging flows where submicron particle deposition and trace metal contamination influence yield, the electronic/EL grade is specified. The material designation appears on the certificate of analysis as Acidic Stripper Electronic/EL Grade with a revision-controlled specification number; the grade suffix is a quality-control term rather than a fixed composition.
Because the product contains a strong acid and hydrogen peroxide, neutralization must be staged. Dilution with water is exothermic; water should be added to the acid solution slowly with continuous stirring, never the reverse. Waste effluent is treated by first reducing residual peroxide with sodium metabisulfite or a dedicated catalytic decomposition unit that controls the reaction temperature below 60°C; the solution is then neutralized with sodium hydroxide or lime slurry to a pH of 6–9 before discharge. Local regulatory permits may impose lower metal discharge limits; therefore no single neutralization procedure is universally applicable. The EL-grade package should be stored away from organic strippers, solvents, bases, and hydroxylamine-containing products; accidental mixing with amine-based developers can cause rapid decomposition and gas evolution. The product must not be used in equipment with exposed titanium parts without specific compatibility confirmation, because acidic peroxide solutions can attack titanium under certain conditions. Materials of construction should be selected from PTFE, PFA, PVDF, quartz, and high-density polyethylene; 316L stainless steel is not recommended for long-term contact because it contributes iron to the bath. Facility exhaust must be compatible with acidic and oxidizing vapors, and the process area should be designed to capture any aerosol generated during spray processing. Waste segregation from organic solvent drains is required to prevent exothermic reactions in mixed waste lines.