| HS Code | 150795 |
| Product Name | Negative PR Developer Electronic/EL Grade |
| Chemical Type | Organic alkaline developer solution |
| Grade | Electronic/EL Grade |
| Appearance | Clear colorless liquid |
| Specific Gravity | 1.00 - 1.02 at 20°C |
| Ph | 13.0 - 14.0 |
| Metal Impurities | Each metal < 1 ppm |
| Particulate Count | ≤ 10 particles/mL (≥ 0.2 µm) |
| Assay | ≥ 99.9% active content |
| Shelf Life | 12 months from date of manufacture |
| Storage Temperature | 15°C to 25°C |
| Application | Development of negative photoresist in semiconductor and electronic manufacturing |
| Packaging | Cleanroom bottles or HDPE containers |
| Safety Hazard | Corrosive; causes skin and eye damage |
As an accredited Negative PR Developer Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Each 1-gallon HDPE container holds Negative PR Developer Electronic/EL Grade, sealed for purity, labeled with handling and safety information. |
| Container Loading (20′ FCL) | 20′ FCL: sealed container with palletized drums of Negative PR Developer Electronic/EL Grade, properly secured and labeled for safe transport. |
| Shipping | Ship as UN1835 Tetramethylammonium hydroxide solution, Class 8 (corrosive), Packing Group II/III. Use properly labeled, leak-proof containers compliant with 49 CFR, IATA, or IMDG. Segregate from acids and oxidizers. Provide safety data sheet, proper shipping documentation, and hazmat-trained personnel for transport. |
| Storage | Store Negative PR Developer Electronic/EL Grade in its tightly sealed original container within a clean, cool, dry, well-ventilated area, ideally at 15–25°C. Protect from light, ignition sources, freezing, and incompatible materials such as strong oxidizers. Keep away from moisture and dust. Ground containers during transfer to prevent static accumulation. Avoid unnecessary opening to preserve purity and shelf life. |
| Shelf Life | Shelf life is typically 12 months from manufacture date when stored unopened in a cool, dark area. |
During wafer-level packaging, negative-tone photoresist is coated at dry film thicknesses between 5 µm and 25 µm and patterned to form electroplating molds for copper redistribution layers and pillar bumps. Where the resist is aqueous-developable, the developer is supplied as 2.38 wt% tetramethylammonium hydroxide and used undiluted; for solvent-developed negative resists, a propylene glycol monomethyl ether acetate or n-butyl acetate blend is used as supplied without dilution. The electronic/EL-grade developer removes the unexposed domains from the resist matrix while the crosslinked network remains as the plating boundary. In production-scale coater/developer tracks, puddle or spray development is performed at 20–25 °C with nozzle pressure held between 0.03 MPa and 0.05 MPa and development time adjusted to resist contrast and thickness. Metal impurities in the developer are critical because residual Na, K, Fe, and Al on the plating seed can migrate into the copper electrodeposit and increase electromigration failure rates. A typical electronic/EL-grade control limit is ≤50 ppb for each critical cation, with total cation burden below 150 ppb by inductively coupled plasma mass spectrometry according to ISO 17294-2:2016. Particle counts for particles at 0.5 µm and larger are maintained below 50 particles/mL when measured with an optical particle counter aligned to ISO 21501-1:2009. The developer is filtered through 0.1 µm rated fluoropolymer membranes in the supply loop to prevent defect formation in fine-pitch RDL structures with line and space critical dimensions below 5 µm. Overdevelopment beyond the vendor-specified endpoint by more than 20% can produce sidewall roughness because the crosslinked matrix begins to swell and delaminate from the copper seed.
| Parameter | Test method / standard | Electronic/EL-grade control limit |
|---|---|---|
| Na | ISO 17294-2:2016 ICP-MS | ≤50 ppb |
| K | ISO 17294-2:2016 ICP-MS | ≤50 ppb |
| Fe | ISO 17294-2:2016 ICP-MS | ≤50 ppb |
| Al | ISO 17294-2:2016 ICP-MS | ≤50 ppb |
| Chloride | ASTM D4327-17 ion chromatography | ≤100 ppb |
| Particles ≥0.5 µm | ISO 21501-1:2009 optical particle counter | ≤50 particles/mL |
| Water content | ASTM E203-16 Karl Fischer titration | ≤0.05 wt% |
Immersion development of SU-8 negative-tone epoxy resists in electronic/EL-grade developer proceeds as a diffusion-limited mass transfer process in features with aspect ratios above 5:1. When a 100 µm thick SU-8 layer is patterned with 10 µm trenches, the unexposed resin at the trench bottom is reached only after the developer front penetrates through a long narrow channel, producing a development rate that decays with trench depth. The electronic/EL-grade developer is used as supplied; dilution is not performed because adding lower-purity solvent raises the particle and metal burden. Megasonic agitation at 1 MHz and temperature control at 21 ± 1 °C are used to stabilize the diffusion boundary layer and reduce residue in blind features. The immersion bath is located in an ISO 14644-1:2015 Class 5 environment to limit particulate contamination during long development cycles. Electronic/EL-grade solvent developer based on propylene glycol monomethyl ether acetate or a proprietary blend is used because higher metal counts generate micro-roughness on vertical sidewalls after plasma descum and can alter electroplating or dry etch uniformity in MEMS actuators and inkjet nozzle plates. Swelling of the crosslinked SU-8 network during development can increase film thickness by 5–15% depending on crosslink density and solvent uptake; prolonged immersion beyond the vendor-defined endpoint should be avoided because swelling induces pattern deformation and crack formation after hard bake. Temperature excursion above 25 °C accelerates swelling and residue hardening, while operation below 18 °C can double the time required for complete clearing. Published development-rate tables for proprietary electronic/EL-grade blends are limited, so endpoint verification is performed on each resist lot by optical inspection of trench base clearing under 50× magnification, with residue-free development at aspect ratios up to 10:1 requiring repeated immersion or spray cycles rather than a single static bath.
Negative-tone solder mask imaging on rigid and flexible printed circuit boards uses an aqueous alkaline developer to remove unexposed mask from surface mount pads, vias, and connector lands. The working solution is prepared at 0.8–1.2 wt% sodium carbonate equivalent and replenished based on throughput and measured pH rather than fixed time intervals. The electronic/EL-grade developer for this segment is filtered to remove particulate matter above 1 µm because residual particles become trapped in solder mask openings and reduce pad wetting during hot air solder leveling or reflow. Spray development equipment with multiple oscillating nozzles operates at 0.8–1.2 bar fluid pressure and 28–32 °C bath temperature; the breakpoint is controlled between 40% and 60% to maintain consistent pad opening dimensions on high-density interconnect boards with solder mask dams down to 50 µm. Metal ion contamination in the developer must be limited because Na and K residues can interfere with electroless nickel immersion gold plating and produce black pad defects. Batch-to-batch variation in developer activity is monitored by titration against a known acid standard. The finished solder mask is qualified to IPC-SM-840E for hardness, adhesion, and chemical resistance. Process engineers should avoid overdevelopment because excessive dwell time undercuts mask edges and widens pad openings beyond the design tolerance; underdevelopment leaves a thin residual layer that inhibits solder wetting.
Electroluminescent and OLED display backplanes use negative-tone photoresist to form pixel definition banks that confine inkjet-printed or spin-coated emissive layers. The developer is used undiluted to avoid shifting the Hansen solubility parameters of the bank resist. The electronic/EL-grade developer removes unexposed bank material from indium tin oxide contact regions where subsequent hole injection layers are deposited. Alkali metal contamination is monitored at ≤10 ppb for Na and K by ISO 17294-2:2016 because mobile ions shift transistor threshold voltage and degrade luminance uniformity in thin-film transistor backplanes. Developer-induced swelling of the bank polymer can change the contact angle of the pixel well and alter the final emissive film thickness profile, so immersion time is limited to the minimum required for complete clearing, typically 45–90 seconds for a 2–3 µm thick bank layer. Puddle development is performed on a vacuum-chucked glass substrate with developer temperature maintained at 23 ± 1 °C. Development time beyond 90 seconds increases bank top rounding and reduces pixel well volume. After development, the substrate is rinsed with deionized water of 18.2 MΩ·cm resistivity and spin-dried under nitrogen to prevent water marks. The developer is supplied in cleanroom-compatible containers and transferred through 0.1 µm rated point-of-use filters to meet particle specifications below 30 particles/mL at 0.5 µm and larger, as measured per ISO 21501-1:2009.
Color filter array patterning for CMOS image sensors uses dyed negative-tone photoresist systems in which the electronic/EL-grade developer removes unexposed matrix from pixel wells with dimensions below 1.0 µm on 300 mm wafers. The developer is used as supplied, with no water dilution. The developer must not introduce sodium, potassium, or iron because metal residues in color filter films increase dark current and reduce photodiode quantum efficiency after the color filter array is planarized. Development is carried out on a wafer track with a low-impact puddle nozzle to protect the soft dyed resist surface from mechanical damage. The puddle dwell time is set between 30 seconds and 60 seconds depending on the color resist type, with developer temperature controlled at 22–24 °C. Overdevelopment beyond 60 seconds can dissolve dyed resist from pixel edges, reducing color purity. After spin-off and rinse, the wafer is dried at 90–110 °C for 60 seconds to stabilize the remaining crosslinked color filter pixels before the next color layer is applied. The electronic/EL-grade developer is monitored for chloride and sulfate by ion chromatography per ASTM D4327-17; anion levels above 100 ppb can cause corrosion of aluminum light shield interconnects during subsequent thermal processing. Resist adhesion to the silicon nitride passivation surface is verified after development by cross-cut tape peel testing according to ISO 2409:2020, with no more than 5% pixel edge loss allowed in production lots.
Compound semiconductor fabs use negative-tone imaging resists to define gate metal lift-off patterns on GaAs and InP HEMT wafers. The exposed resist crosslinks to form a stable template for e-beam or sputter deposition of gate metals such as Ti/Pt/Au. The electronic/EL-grade developer removes the unexposed resist after exposure and post-exposure bake, leaving an undercut profile that controls metal discontinuities at the resist edge. The solvent developer is used undiluted; moisture pickup from ambient must be controlled because water contamination modifies the dissolution rate and undercut angle. Development is performed by immersion or spray with solvent-based developer at 20–25 °C for 60–120 seconds, followed by a rinse in a compatible solvent and nitrogen blow-off. Metal impurity control is critical because residual Fe and Ni can form deep-level traps in GaAs and degrade high-frequency gain. The developer is specified with individual transition metal concentrations below 25 ppb by ISO 11885:2007 or ISO 17294-2:2016. Particle counts above 0.5 µm are limited to 50 particles/mL to prevent gate finger opens on sub-100 nm gate length devices. After metal evaporation and lift-off, the remaining resist is removed in a separate stripper; incomplete development before metal deposition creates residual foot at the gate base that increases contact resistance. The undercut profile is verified by scanning electron microscopy at 30,000× magnification, and the developer batch is retested for water content by Karl Fischer titration per ASTM E203-16 when the bottle has been open for more than 72 hours to control moisture uptake from the cleanroom ambient.
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Negative PR Developer Electronic/EL Grade, model NPD-EL 2000, is a high-purity solvent developer formulated for the selective removal of unexposed negative-tone photoresist films in semiconductor packaging, microelectromechanical systems, flat-panel display lift-off, and thick-film plating processes. The product is supplied as a controlled blend of n-butyl acetate and xylene isomers with a minimum assay of 99.90% by gas chromatography. It is filtered through 0.1 µm polytetrafluoroethylene membrane media and filled in an ISO 14644-1 Class 5 cleanroom into fluoropolymer-lined stainless steel containers. The development mechanism is differential: non-crosslinked cyclized-polyisoprene or epoxy-based negative resist domains are solvated and removed, while exposed and crosslinked regions remain adhered to the substrate. Because the developer is solvent-based rather than aqueous alkaline, it avoids alkaline attack on aluminum and copper interconnect metallization and is compatible with thick resist films in the 5 µm to 25 µm range. The material is a flammable liquid with a closed-cup flash point below 25 °C, requiring explosion-proof process equipment, local exhaust ventilation, moisture exclusion, and separation from amine-bearing rework chemicals.
The principal differences appear in trace-metal, water, and particle control. General-purpose solvent developers may contain total metals in the 1–10 ppm range, water above 0.1%, and particle counts exceeding 100 counts/mL at 0.5 µm. Electronic/EL Grade NPD-EL 2000 is controlled to total metal cations of ≤25 ppb by inductively coupled plasma mass spectrometry after solvent evaporation, with individual cation limits of ≤5 ppb for sodium, potassium, calcium, iron, chromium, nickel, copper, and zinc. Chloride and sulfate are each held ≤50 ppb by ion chromatography after aqueous extraction. Water is limited to ≤300 ppm by ASTM D1364 Karl Fischer coulometry, and nonvolatile residue is ≤5 ppm by ASTM D1353. Color is ≤5 APHA by ASTM D1209. Acidic impurities, reported as acetic acid, are ≤50 ppm by ASTM D1613. The particle specification is ≤25 counts/mL at 0.5 µm and ≤1 count/mL at 1.0 µm, measured by laser particle counting in an ISO Class 5 sample-transfer hood. These limits are relevant because residual sodium and potassium ions can migrate into gate oxides and shift threshold voltage, while particles above 0.5 µm generate post-develop residue at the base of high-aspect-ratio trenches.
| Parameter | Method | Release Limit |
|---|---|---|
| Assay as n-butyl acetate plus xylene isomers | GC-FID | 99.90% minimum |
| Water | ASTM D1364 | ≤300 ppm |
| Color | ASTM D1209 | ≤5 APHA |
| Acidity as acetic acid | ASTM D1613 | ≤50 ppm |
| Nonvolatile residue | ASTM D1353 | ≤5 ppm |
| Particles at 0.5 µm | Laser particle counter | ≤25 counts/mL |
| Particles at 1.0 µm | Laser particle counter | ≤1 count/mL |
| Total metal cations | ICP-MS after evaporation | ≤25 ppb |
| Sodium, potassium, calcium, iron, chromium, nickel, copper, zinc | ICP-MS after evaporation | ≤5 ppb each |
| Chloride | Ion chromatography after extraction | ≤50 ppb |
| Sulfate | Ion chromatography after extraction | ≤50 ppb |
Application of NPD-EL 2000 on production lines differs from positive aqueous development in that the developing tank must be explosion-proof and the substrate must enter the developer free of water droplets. A representative sequence for 12 µm cyclized-polyisoprene negative resist includes prebake at 95 °C for 120 s, broadband exposure at 365–405 nm with a dose of 200–600 mJ/cm², post-exposure bake at 110 °C for 90 s, and development at 23 °C for 90 s in immersion mode or 4 spray-puddle cycles. Rinse is performed with electronic-grade n-butyl acetate for 30 s followed by filtered nitrogen spin-drying. The negative-tone mechanism leaves the exposed region crosslinked and the unexposed region dissolved, so mask polarity is reversed relative to positive-tone diazonaphthoquinone resists. For lift-off processing, the undercut profile is smaller than for positive resists; production layouts commonly add 0.5–1.0 µm design bias to compensate for the reduced isotropic dissolution. The product is not intended as a stripper; removal after metallization should use a separate solvent stripper such as N-methyl-2-pyrrolidone or a commercially formulated negative resist stripper.
Development temperature is specified at 23 °C ± 2 °C. A drop below 18 °C reduces development rate by approximately 25–30% and extends immersion time, while temperatures above 28 °C may induce swelling of the crosslinked region and critical-dimension loss. A production control range of ≤ ±5 °C is therefore established for recirculating stainless steel heat exchangers. For spray-puddle tools, nozzle pressure should be held at 1.5–2.0 bar and puddle cycles at 3–5 cycles per wafer or panel. For immersion development, a 60–120 s bath residence time is typical for 10 µm cyclized-polyisoprene resist at 23 °C; resist films above 20 µm may require 180–240 s with mild ultrasonic agitation not exceeding 40 kHz to reduce cavitation damage. Equipment wetted surfaces should be stainless steel, polytetrafluoroethylene, or polypropylene. Brass, copper, zinc, and amine-cured elastomers should be excluded because copper ions at 10 ppb can quench acid diffusion in chemically amplified negative resists, and amines neutralize photoacid generators. Diaphragm pumps with polytetrafluoroethylene wetted parts and perfluoroelastomer O-rings are recommended. Condensation in unblanketed drums can raise water content from 250 ppm to 700 ppm within 72 h at 60% RH; nitrogen blanketing at 0.2–0.5 bar head pressure is specified for bulk feed lines.
Replacing 2.38% tetramethylammonium hydroxide positive developer with NPD-EL 2000 is indicated when aluminum or copper traces are exposed during development. Alkaline tetramethylammonium hydroxide attacks aluminum at high pH, producing interfacial undercut and hydrogen gas, whereas NPD-EL 2000 has no measurable alkalinity and is formulated to avoid dissolution of aluminum, copper, and silicon oxide at 23 °C for immersion times up to 5 minutes. Compared with standard solvent negative developers, the Electronic/EL Grade reduces post-rinse residue through its nonvolatile residue limit of ≤5 ppm, its water limit of ≤300 ppm, and its narrower boiling-point distribution of 124–128 °C. The narrower boiling distribution reduces variable evaporation from open immersion baths and maintains more stable development-rate profiles across shifts. Standard solvent negative developers with water at 500–1000 ppm can generate visible resist scum at the base of high-aspect-ratio trenches; the EL Grade is controlled below that threshold. Table 2 summarizes the comparative specification boundaries.
| Parameter | Electronic/EL Grade NPD-EL 2000 | Standard solvent negative developer | 2.38% TMAH positive developer |
|---|---|---|---|
| Developer type | Solvent negative-tone | Solvent negative-tone | Aqueous alkaline positive-tone |
| Alkalinity | None | None | pH 13 |
| Water | ≤300 ppm | Often 500–1000 ppm | Not applicable |
| Total metals | ≤25 ppb | Typically 1–10 ppm | Typically ≤100 ppb if electronic grade |
| Particles at 0.5 µm | ≤25 counts/mL | Often >100 counts/mL | Usually ≤50 counts/mL |
| Aluminum compatibility | Pass at 23 °C for 5 min | Variable; may contain free acid or chloride above 1 ppm | Attacks aluminum |
| Resist tone polarity | Negative: exposed areas remain | Negative: exposed areas remain | Positive: exposed areas dissolve |
| Main residue risk | Low; controlled NVR and water | Scum from water and metals | Alkaline salts on metal surfaces |
Operational boundaries are explicit. The developer should not be combined with amine-based additives, water-based developers, or positive-resist stripping solutions because trace amines neutralize photoacid in chemically amplified negative resists and water above 500 ppm increases interfacial residue. Pre-drying of air lines and nitrogen blanketing is required when ambient relative humidity exceeds 60% for more than 4 h. The product is classified as flammable liquid category 2 under GHS, with closed-cup flash point 25 °C specified by ASTM D56. Storage beyond 12 months is not recommended without re-certification of water and particle limits. Published data for applications involving nonstandard substrates or chemically amplified epoxy formulations is limited; process qualification should therefore include electrical test structures and lift-off profile verification on the specific production layer stack.