| HS Code | 338614 |
| Productname | Lift-off photoresist remover Electronic/EL Grade |
| Chemicaldescription | Electronically pure N-methyl-2-pyrrolidone (NMP)-based organic remover |
| Appearance | Clear colorless liquid |
| Odor | Mild, characteristic solvent odor |
| Physicalstate | Liquid at room temperature |
| Boilingpoint | Approximately 202 °C |
| Flashpoint | Approximately 91 °C (closed cup) |
| Density | Approximately 1.03 g/cm³ at 20 °C |
| Viscosity | Approximately 1.65 mPa·s at 25 °C |
| Vaporpressure | Approximately 0.29 mmHg at 20 °C |
| Solubilityinwater | Miscible |
| Refractiveindex | Approximately 1.469 at 20 °C |
| Puritygrade | Electronic/EL high-purity grade |
| Watercontent | ≤ 0.1% |
| Metalioncontent | Controlled to ppb levels |
| Filtration | Filtered to 0.2 µm |
| Shelflife | 12 months in original sealed container |
| Storagetemperature | 15 °C to 35 °C |
As an accredited Lift-off photoresist remover 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 (3.78 L) high-density polyethylene bottle with secure cap, labeled for Electronic/EL Grade lift-off photoresist remover. |
| Container Loading (20′ FCL) | 20′ FCL: secure chemical drums/IBCs upright, compatible segregation, proper labeling, bracing and dunnage for safe transport of Electronic/EL Grade remover. |
| Shipping | Lift-off photoresist remover (Electronic/EL grade) is shipped as a hazardous material, typically UN 1993, Flammable Liquid, Class 3, Packing Group II or III. It requires UN-certified containers, hazard class labels, and proper shipping documentation under applicable transport regulations. |
| Storage | Store in a tightly sealed original container in a cool, dry, well-ventilated area away from sunlight, heat, and ignition sources. Keep separate from oxidizers and incompatible chemicals. Avoid moisture contamination to preserve Electronic/EL Grade purity. Ensure container remains upright and grounded if flammable, with proper labeling and secondary containment. |
| Shelf Life | Shelf life is typically 2 years from manufacture date when stored sealed in original container at room temperature. |
At the redistribution-layer lift-off stage, the negative-tone resist film is deposited to 25–50 µm and then removed after electrolytic Cu pillar and Ni/Au cap deposition. The electronic/EL-grade remover used in this pathway is a water-lean blend of polar aprotic solvent at 55–75 wt%, alkanolamine at 20–35 wt%, azole corrosion inhibitor at 0.1–1.0 wt%, and water held below 0.3 wt% by ASTM D1364-02 Karl Fischer measurement. The immersion bath operates at 70–85°C in a quartz recirculation tank fitted with 0.1 µm PTFE filtration, nitrogen blanketing, and megasonic agitation in the 700–900 kHz band. Metal impurity control follows inductively coupled plasma mass spectrometry after EPA Method 200.8 preconcentration, with Na, K, Fe, Cu, and Zn individually maintained at ≤10 ppb. Chloride is measured by ASTM D512-23 and controlled below 100 ppb, while particles larger than 0.2 µm remain below 100 counts/mL when sampled under ISO 21501-4:2018. The dominant process conflict is not bulk resist dissolution but nickel cap corrosion: if bath pH exceeds 11.6, witness coupon testing shows nickel etch above 0.5 nm/min. Addition of the azole inhibitor at 0.3 wt% suppresses nickel etch to below 0.1 nm/min without extending the 30–40 min target strip time. Post-strip rinsing uses Type E-1 water per ASTM D1193-06 in a two-stage overflow cascade followed by isopropanol. The terminal device is a wafer-level chip-scale package carrying 30–40 µm pitch Cu pillars with Ni/Au caps, where residual organic ash on pad surfaces must remain below 10 µg/cm² by TOF-SIMS to avoid non-wetting during reflow.
| Parameter | Test method / instrument | Electronic/EL-grade control limit |
|---|---|---|
| Na, K, Fe, Cu, Zn | ICP-MS, EPA Method 200.8 | ≤10 ppb each |
| Chloride | ASTM D512-23 | ≤100 ppb |
| Sulfate | ASTM D516-22 | ≤200 ppb |
| Water | ASTM D1364-02 | ≤0.3 wt% |
| Particles ≥0.2 µm | ISO 21501-4:2018 | ≤100 counts/mL |
For surface-micromachined MEMS acoustic transducers, a gold electrode is lifted off from an aluminium or AlSiCu bond pad, and the wet stripper must dissolve an 8–12 µm positive-tone image-reversal resist at 45–60°C while holding aluminium etch to <0.1 nm/min because the pad thickness is often only 500–800 nm. The chemistry for this segment is a buffered formulation with lower alkanolamine content than advanced packaging: alkanolamine 8–15 wt%, polyhydric alcohol 40–60 wt%, deionized water 20–30 wt%, and a pyridine-free corrosion inhibitor at 0.5–2.0 wt%. Bath pH is held between 9.8 and 10.4, and witness wafer data indicate that pH above 10.6 produces aluminium loss exceeding 0.3 nm/min under identical immersion conditions. The process equipment is a static immersion vessel with 950 kHz megasonic transducers operated below 10 W/cm² to avoid cavitation damage on released MEMS structures. Cleanroom handling conforms to ISO 14644-1:2015 Class 5 conditions, and the remover is controlled to tighter cation limits than standard electronic grade because mobile ion accumulation shifts transducer bias voltage. Sodium and potassium are required below 5 ppb each. After stripping, wafers are rinsed in Type E-1 water and dried under filtered nitrogen. The terminal component is a capacitive micromachined ultrasonic transducer or microphone with 0.2–0.5 µm Au electrodes, where trace metal residue above 10⁹ atoms/cm² alters resonant frequency and pull-in voltage.
In power semiconductor contact metallization, Ti/Ni/Ag stacks impose a different constraint: the remover must not leave sulfur-bearing residue or chloride-induced nickel corrosion in the contact trench. The electronic-grade stripper for this application is formulated with polar aprotic solvent at 60–75 wt%, alkanolamine 15–25 wt%, a sulfur-free organic inhibitor below 0.5 wt%, and a chelating agent at 1–3 wt% to sequester dissolved silver. The bath operates at 60–70°C for 15–25 min, and total dissolved metal loading is controlled below 50 mg/L because silver loading above this threshold precipitates as colloidal AgCN or Ag2S microcontamination on wafer surfaces. Compliance is verified by chloride below 100 ppb per ASTM D512-23 and sulfate below 200 ppb per ASTM D516-22. For 150 mm and 200 mm batch immersion, carrier agitation is maintained at 0.5–1.0 m/s linear velocity to prevent boundary-layer depletion at the base of 0.4–0.8 µm contact trenches. A direct process conflict appears at higher temperature: at 75°C, silver etch rate can exceed 0.2 nm/min, and SEM cross-sections reveal cratering of the underlying TiW layer. The output is the front-side Schottky or ohmic contact window on power devices prior to backside metallization; residual chloride above 100 ppb in the gate region is rejected because it propagates electrochemical migration during biased humidity testing.
Micro-LED array metallization lift-off uses evaporated metal stacks on 5–10 µm thick positive resist with undercut sidewalls, and single-wafer spray processing is preferred over batch immersion because immersion can leave residue in 2–5 µm pixel gaps. The remover formulation for spray application has viscosity below 3 cP at 25°C and is composed of aprotic solvent 70–85 wt%, alkanolamine 5–10 wt%, nonionic surfactant 0.05–0.2 wt%, and water below 0.5 wt%. The process sequence consists of pre-wetting with Type E-1 water, dispensing at 60–80°C through a fan nozzle, and nitrogen atomization at 2.5–5.0 bar. The lower pressure boundary is critical because below 2.5 bar the mechanical shear is insufficient to clear metal flakes from the undercut edge, and optical inspection at 20× magnification identifies sidewall residue on more than 30% of pixels. The remover is passed through 0.05 µm polypropylene capsules immediately before dispense, and particle counts are maintained below 50 particles/mL at 0.2 µm apparent size. Metal impurity limits follow ICP-MS with ≤5 ppb for Cu, Fe, and Zn because these elements reduce radiative recombination efficiency if they remain in the peripheral oxide. The terminal devices are GaN or AlInGaP micro-LED chips with pixel pitch down to 8 µm, and residual carbon at the pixel sidewall must remain below 5 at.% by XPS to prevent dark-line defect growth during current aging.
For advanced organic substrates using ABF film or other build-up dielectrics, the semi-additive process deposits flash-seed copper, pattern-plates the circuit, and then removes the flash layer in a lift-off remover that must not swell the dielectric. The EL-grade chemistry for this application is a near-anhydrous blend of dimethylacetamide-type solvent at 65–80 wt%, glycol diether 10–20 wt%, alkanolamine 3–8 wt%, and a bond-pad-compatible inhibitor at 0.2–0.5 wt%. Water is kept below 0.2 wt% by Karl Fischer to avoid ABF swelling and subsequent line-width widening. The process is run in a conveyorized spray chamber at 35–45°C, chamber pressure of 0.3 MPa, and stage speed of 0.8–1.2 m/min. The low amine and low water levels are critical because ABF absorbs polar solvent at elevated temperature, causing 2–5% thickness increase measured by ellipsometry; above 45°C, dielectric surface roughness increases and subsequent electroless copper adhesion falls below 4B in ASTM D3359-23 tape testing. After stripping, panels receive a three-stage cascade rinse, citric acid neutralization, and air-knife drying. Published data for specific ABF swelling in this exact chemistry is limited, so production qualification relies on panel witness testing rather than vendor extrapolation. The terminal structure is a 1.5 µm line/space redistribution layer on advanced IC substrate, where residual chloride is controlled below 50 ppb to avoid electrochemical migration under 85°C/85% RH biased humidity testing.
During RF SAW filter fabrication, aluminium-copper interdigital transducer lift-off requires a low-alkali formulation because transducer fingers are 0.3–0.8 µm wide and 150–300 nm thick. The electronic/EL-grade stripper for this segment is pH-buffered between 9.0 and 9.6 with alkanolamine 5–10 wt%, polyol 30–45 wt%, water 10–20 wt%, and a surfactant package 0.05–0.15 wt%. The bath is operated at 40–50°C for 10–20 min without megasonic or ultrasonic energy because cavitation on quartz substrates can detach finger edges. The remover is supplied in 0.1 µm filtered containers and held to ≤10 ppb each of Na, K, Ca, and Al by ICP-MS. Particles above 0.2 µm are controlled below 80 counts/mL; particles adhering to the IDT sidewall alter acoustic velocity and increase center-frequency scatter. Rinsing uses a cold-DI cascade followed by controlled nitrogen spin-dry. The output is an RF SAW filter with Al-Cu electrodes on lithium tantalate or quartz, and the lift-off step is considered acceptable only if post-strip linewidth loss is below 5 nm per edge by CD-SEM.
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TechniStrip Lift-Off II, Electronic/EL Grade is formulated as an N-methyl-2-pyrrolidone-free and amine-free solvent blend for post-metallization lift-off in wafer-level MEMS, compound semiconductor, and advanced packaging lines. The product is supplied in 1 L, 4 L, and 20 L high-density polyethylene containers with a nitrogen headspace to limit water absorption during storage. The electronic/EL grade designation reflects acceptance criteria for trace metal cations, chloride, and particles that are compatible with Al, Cu, Ni, Au, Pd, and ITO metallizations. In a typical immersion process, the remover is held at 60 °C to 80 °C in a recirculating bath and dissolves positive-tone diazonaphthoquinone/novolac resist films after metal evaporation; lift-off is completed when swelled resist releases from the underlying sacrificial layer. The formulation is intended for use where technical-grade NMP strippers leave ionic residues on bond pads or where amine-containing removers attack copper seed layers. Published data for this specific configuration is limited; the following sections identify the analytical methods, process boundaries, and comparative differences that are documented in the manufacturer’s technical bulletin and standard electronic chemical qualification protocols.
The electronic/EL grade is controlled by a specification that is tighter than standard technical-grade formulations. The acceptance ranges shown in Table 1 are typical for a product designed to support lift-off on ≤ 200 mm wafers and 150 mm compound semiconductor substrates. Viscosity and specific gravity are monitored because they affect bath turnover and resist dissolution rate. pH is controlled to avoid excess alkaline hydrolysis of novolac, while water content is limited to reduce copper-oxide formation during prolonged immersion. Trace cation limits are established by SEMI C8-1114 inductively coupled plasma mass spectrometry after closed-vessel acid digestion; the <50 ppb per-cation ceiling is lower than the 1–5 ppm Na and Fe values commonly observed in technical-grade NMP.
| Property | Method/Standard | Acceptance Range |
|---|---|---|
| Appearance at 25 °C | Visual inspection | Clear, colorless to pale yellow |
| Specific gravity at 25 °C | ASTM D4052 | 1.03–1.06 |
| Viscosity at 25 °C | ASTM D445 | 8–12 cP |
| pH as-is | ASTM D1287 | 9.5–11.5 |
| Closed-cup flash point | ASTM D93 | > 100 °C |
| Water content | ASTM E203 | < 0.5 wt% |
| Chloride | Ion chromatography per ASTM D4327 | < 100 ppb |
| Na, K, Ca, Fe, Cu | SEMI C8-1114 ICP-MS | < 50 ppb each |
| Particles ≥ 0.5 µm | Laser particle counter | < 10 particles/mL |
| Volatile organic compound content | EPA Method 24 | < 100 g/L |
Particle control is a critical specification because loosened resist solids can re-adhere to the metal surface during rinse. The <10 particles/mL limit at ≥ 0.5 µm is verified by a laser particle counter with a 10 mL/min sampling rate; filtration through 0.2 µm polytetrafluoroethylene cartridges maintains that value during production. The cation limits are relevant to GaAs and GaN lift-off, where sodium and potassium migration can alter threshold voltage drift under 85 °C/85% RH bias. A second analytical verification by ion chromatography per ASTM D4327 is used for chloride, nitrate, and sulfate; chloride is kept below <100 ppb because chloride promotes pitting on Al-Cu bond pads during downstream wire bonding. Flash point above 100 °C by ASTM D93 permits heated immersion in non-explosion-proof enclosures, but the tank exhaust must still maintain a solvent vapor concentration below 25% of the lower flammable limit.
In production immersion tools, the remover is charged into a 316L stainless steel or fluoropolymer tank of 20–50 L capacity with an external magnetic-drive pump. The pump is operated at 1–2 bath turnovers per hour through 0.2 µm PTFE filters; higher flow rates can generate air bubbles that collapse on the wafer surface and cause pitting in thin copper seed layers. A nitrogen blanket on the tank reduces dissolved oxygen below 2 ppm, which extends the bath life by slowing copper oxide formation. The immersion temperature is controlled to ±5 °C around the 70 °C set point using a thermowell and PTFE-coated immersion heater. If the bath exceeds 85 °C, the copper etch rate rises above <0.1 nm/min and the dissolution rate of positive resist increases by 10–15% per 10 °C, causing undercutting of fine Au/Ti lift-off patterns.
Ultrasonic transducers operating at 40 kHz with a power density of 15–25 W/L reduce lift-off time for 1–3 µm evaporated aluminum patterns. Power densities above 30 W/L create standing waves that can delaminate sputtered Cr/Au test structures. Batch-to-batch variance in residue removal is controlled by recording bath age, water content, and particle counts; replenishment is typically performed at 20% volume loss with filtered make-up. Transfer from the remover bath to a deionized water dump-rinse should occur within 30 s to avoid redeposition of dissolved resist solids. A cascade rinse of two or three stages with overflow rates of 1–2 L/min removes most residual solvent; final spin-rinse drying is carried out under nitrogen at 1,500–2,000 rpm for 60 s.
The remover is stored in original high-density polyethylene containers at 15 °C to 25 °C; shelf life is 12 months from the date of manufacture when the container remains sealed. In unopened containers, water content remains below 0.5 wt% for the shelf-life period. After opening, the container should be blanketed with nitrogen or argon and sealed within 5 min to prevent moisture uptake. The liquid is compatible with 316L stainless steel, fluorinated ethylene propylene, polypropylene, and high-density polyethylene; it is not compatible with Viton elastomers, which swell more than 10% by volume after 24 h at 60 °C. Piping and diaphragm materials should be verified by immersion coupon tests; EPDM and perfluoroelastomer seals are preferred over nitrile.
At operating temperature, the remover has a vapor pressure below 1 mmHg at 25 °C, and the closed-cup flash point is above 100 °C. Local exhaust ventilation must still be provided at the tank lip to maintain the vapor concentration below 25% of the lower flammable limit. The bath should not be mixed with strong oxidizing agents, including hydrogen peroxide, nitric acid, or piranha, because exothermic decomposition can occur. Spent remover is classified as organic solvent waste and should be shipped for solvent incineration at temperatures above 1,100 °C; pH adjustment and chemical oxygen demand reduction are required before any controlled aqueous discharge permitted by local wastewater regulations.
The absence of N-methyl-2-pyrrolidone removes the reproductive toxicity classification under EU CLP and simplifies waste segregation under REACH. Technical-grade NMP lift-off strippers require solvent waste disposal and often leave organic carbon residue above 10 µg/cm² on aluminum bond pads after rinse. DMSO-only lift-off recipes at 80 °C swell diazonaphthoquinone/novolac films but do not completely dissolve crosslinked edge beads; the Electronic/EL Grade contains a proprietary co-solvent package that reduces residual film thickness to below 0.5 nm on silicon oxide when monitored by spectroscopic ellipsometry. Amine-containing strippers remove negative-tone resists faster but attack copper at rates above 1 nm/min at 70 °C; the amine-free formulation limits copper etch to <0.1 nm/min in a 60 min immersion. The product also avoids hydroxylamine, which can decompose exothermically above 100 °C in closed containers. Compared with acetone or isopropanol soak processes, the Electronic/EL Grade does not require explosion-proof cooling and leaves no white carbon residue on high-aspect-ratio gold pillars after air dry.
The difference in residue chemistry is measurable by sessile-drop water contact angle per ASTM D7334; a clean Al pad after the Electronic/EL Grade and rinse typically shows a contact angle below 10°, while NMP-based lifts often leave hydrophobic residues that increase contact angle above 30°. For lift-off of 200 nm sputtered gold on sacrificial resist, the remover is used as a single-step process, whereas DMSO-only often requires a subsequent oxygen plasma descum to reach acceptable wire-bond pull strength. Published data for this specific configuration is limited, but production lines using the product commonly report 0.5–1.0 µm line/space lift-off capability. The Electronic/EL Grade is also compatible with Cu pillar bumping, where chloride and sulfur residues must remain below wire-bond failure thresholds.
Ultrasonic energy is calibrated with a broadband hydrophone or aluminum foil erosion test according to the tank manufacturer’s qualification procedure. A 40 kHz ultrasonic field creates cavitation at the metal/resist interface; the resulting microjets peel the swelled resist from the metal surface but also fatigue thin free-standing gold membranes. For 200 nm sputtered gold on a sacrificial resist, ultrasonic power should be limited to 10–15 W/L; at 25 W/L, acoustic streaming can produce 0.5 µm undercutting at the anchor. Wafer rotation in a spray processor at 20–50 rpm can replace ultrasonic immersion for fragile structures; spray pressure at 1.5–2.0 bar is used with the same chemistry at 60 °C.
The processing window of ±5 °C around the 70 °C set point is applied because dissolution rate changes roughly 10–15% per 10 °C, and copper attack rises above the <0.1 nm/min limit at 85 °C. Bath temperature non-uniformity should be measured at the heater inlet, tank center, and filter return; a differential above 3 °C indicates insufficient recirculation or heater fouling. For Al line widths below 2 µm, ultrasonic energy is often avoided entirely; a heated immersion process with gentle overflow agitation at 60 °C for 45–60 min provides lift-off without metal damage. For pillars and bumps with 50 µm pitch, spray processing at 1.5–2.0 bar and 60 °C clears resist from the base without mechanical scrubbing. The cavitation intensity should not be increased beyond 25 W/L to compensate for exhausted chemistry; instead, the bath should be replenished or replaced based on particle counts and water content.
On copper redistribution layers with 2 µm line pitch, the remover is qualified by shear testing of 30 µm diameter copper pillars after lift-off and rinse. The acceptance criterion is die shear strength above 10 MPa and failure within the epoxy molding compound, not at the pillar interface, when tested per MIL-STD-883 Method 2019 with a 100 N load cell at 25 °C. For aluminum bond pads, the remover must not increase surface roughness by more than 0.5 nm RMS as measured by atomic force microscopy per ASTM E2859 over a 5 µm × 5 µm scan area. Process capability is monitored by ellipsometric thickness of the sacrificial lift-off layer before and after exposure; a residual thickness above 0.5 nm indicates incomplete removal or redeposition. The product is not recommended for lift-off of thick SU-8 negative resists without an oxygen plasma descum step.
Rinse verification is performed by extracting a 100 cm² wafer sample in 10 mL of ultrapure water at 80 °C for 60 min and measuring total organic carbon by oxidation/NDIR per ASTM D7573. Electronic/EL Grade lift-off processes are qualified when TOC is <0.5 µg/cm² and surface cations are <1×10¹¹ atoms/cm² by time-of-flight secondary ion mass spectrometry. The remover’s metal impurity levels are tested per SEMI C8-1114, while anion contamination is monitored by ion chromatography per ASTM D4327. The product is not recommended for immersion of unprotected silver electrodes; silver requires sulfide-free formulations. Incompatibilities include strong oxidizing acids such as piranha, which react exothermically with solvent residues, and amine-based additives that raise the pH above 12.5 and increase copper etch. Moisture absorption above 0.5 wt% alters the flash point and increases metal-oxide growth on copper, so the container headspace must be resealed after each transfer.
In analytical verification, the extraction solution is analyzed for Na, K, Ca, Fe, Cu, and Zn by ICP-MS; the acceptance threshold for each cation is <1 ng/cm² on 150 mm wafer surfaces. This is stricter than the bulk product specification because the rinse must remove any residue that may have been concentrated during evaporation. Particle residues after rinse are quantified by scanning electron microscopy review of 5 die per wafer at 10 kV; visible resist fragments above 0.2 µm require rework. Product changeover from NMP-based strippers to this Electronic/EL Grade requires a complete tank rinse and replacement of filter elements, because residual NMP can alter flash point and leave carbon residue on downstream devices. The bath is replaced after accumulated solids reach 0.5 g/L or after 200 wafer-equivalent cycles, whichever occurs first.