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TMAH (Tetramethylammonium Hydroxide) Anji Microelectronics

    • Product Name: TMAH (Tetramethylammonium Hydroxide) Anji Microelectronics
    • 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 414885
    Product Name TMAH (Tetramethylammonium Hydroxide)
    Manufacturer Anji Microelectronics
    Chemical Formula (CH3)4NOH
    Cas Number 75-59-2
    Molecular Weight 91.15 g/mol
    Appearance Clear colorless liquid
    Concentration Aqueous solution (semiconductor-grade, typically around 2.38% for photoresist developer use)
    Density Approximately 1.00 g/cm³ at 25°C
    Ph Strongly alkaline, approximately 13
    Solubility In Water Miscible
    Boiling Point Aqueous solution boils near 100°C with decomposition at higher temperatures
    Metal Impurity Level Ultra-low trace metal content suitable for semiconductor processing

    As an accredited TMAH (Tetramethylammonium Hydroxide) Anji Microelectronics factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing TMAH (Tetramethylammonium Hydroxide) from Anji Microelectronics is supplied in sealed HDPE drums, 25 kg per container, for semiconductor use.
    Container Loading (20′ FCL) A 20′ FCL container loaded with TMAH from Anji Microelectronics, securely packed, labeled, and transported per hazardous chemical regulations.
    Shipping TMAH (Tetramethylammonium Hydroxide) from Anji Microelectronics is shipped as hazardous material UN1835, Class 8 corrosive liquid. Transport requires leak-proof, corrosion-resistant packaging, proper labeling, and documentation. It must be kept separate from acids and oxidizers, with trained handlers per IMDG/ADR/DOT regulations. Store and transport upright, sealed, away from incompatible materials.
    Storage Store TMAH (Tetramethylammonium Hydroxide) from Anji Microelectronics in tightly sealed original containers, in a cool, dry, well-ventilated area away from direct sunlight, heat, acids, and oxidizing agents. Maintain stable temperature above 15°C to prevent crystallization. Keep containers upright and clearly labeled. Use secondary containment and proper PPE to prevent leaks or skin contact.
    Shelf Life Store in original sealed container at room temperature, away from light and heat. Shelf life: typically 6–12 months from manufacture date.
    Application of TMAH (Tetramethylammonium Hydroxide) Anji Microelectronics

    In advanced-node integrated circuit fabrication, Anji Microelectronics tetramethylammonium hydroxide is supplied as a 25 wt% electronic-grade aqueous solution and diluted at the point of distribution to the standard positive photoresist developer normality of 0.26 N, corresponding to 2.38 ± 0.02 wt% TMAH in ultrapure water. The dilution line is fed with water maintained at 18.2 MΩ·cm resistivity and total organic carbon below 5 ppb; cation impurities in the diluted developer are controlled under SEMI C18 electronic-grade TMAH specifications, with verification by inductively coupled plasma mass spectrometry for Na, K, Fe, Al, and Zn. The point-of-use dispense path includes 0.05–0.10 µm PTFE membrane filtration and nitrogen blanketing to limit carbon dioxide uptake, because dissolved carbonate species shift the hydroxide equilibrium and increase the probability of organic residue formation on chemically amplified resists. The developer is consumed in single-pass mode on advanced tracks; recirculating bowls are avoided at nodes where particle or metal accumulation would shift critical dimension uniformity beyond the acceptable process limit. The production process proceeds through hexamethyldisilazane vapor prime, positive-tone DNQ-novolac or chemically amplified resist spin coating, soft bake, exposure on 193 nm or 248 nm scanning steppers, post-exposure bake, puddle or dynamic spray development for 30–60 s at 23 ± 0.2°C, deionized water rinse, and spin dry. Aluminum bond pads and exposed copper are masked or protected during development because TMAH is sufficiently alkaline to attack unprotected aluminum and create uncontrolled metal loss. The downstream terminal products comprise logic, dynamic random-access memory, NAND flash, CMOS image sensors, and analog/mixed-signal wafers in which mobile ion contamination at single-digit parts-per-billion levels is a yield-limiting parameter.

    On production-scale coater/developer tracks configured for 300 mm wafers, failures associated with TMAH feed variation are most commonly observed as center-to-edge linewidth gradients caused by developer temperature drift or by aging in the point-of-use line after idle periods. A developer bath with carbonate uptake above control limits produces a measurable drop in pH and leaves a residue at the exposed-unexposed boundary; inline concentration verification by refractive index or conductivity is therefore used after each batch change. The acceptable batch-to-batch concentration variance must remain within ±0.02 wt% to keep post-development feature width stable at tight design rules. The use of 25 wt% TMAH stock rather than pre-diluted product is preferred for large fabs because the higher concentration reduces transportation weight and permits point-of-use proportioning into 2.38 wt% developer, but dilution skid design must prevent localized heating from exothermic mixing.

    What Governs Large-Format Photoresist Development Uniformity in Array Lithography?

    Flat panel display array processing uses TMAH developer at 2.38 ± 0.03 wt% in ultrapure water for positive-tone DNQ-novolac photoresists on glass substrates. In a Gen 8.5 or Gen 10.5 line, the substrate size reaches 2940 mm × 3370 mm; developer is prepared by inline mixing of 25 wt% TMAH stock with ultrapure water at a mass ratio of approximately 9.5:1 water to stock. Chemical purity is governed by SEMI C18 electronic-grade TMAH specifications, and the array lithography environment is maintained at ISO 14644-1 Class 4–6 depending on the layer. Point-of-use particle monitoring with an on-line laser particle counter maintains particles ≥0.5 µm at or below 50 counts/mL before the dispense nozzle. The developer is dispensed through a horizontal slit nozzle that sweeps across the glass surface within an inline development chamber; the process sequence includes detergent clean, adhesion promoter coating, resist slit coating, vacuum drying, low-temperature pre-bake, mask exposure, development for 40–90 s at 23 ± 1°C, high-pressure DI rinse, air-knife drying, and post-bake. In field operation, the dominant yield-limiting failure is not bulk concentration but local developer loading in high-open-area regions; exhausted developer at the resist-glass interface slows dissolution and creates line edge roughness and Mura-type streaks. Therefore, the development unit maintains a minimum liquid exchange rate per substrate and uses nitrogen-blanketed buffer tanks to prevent carbonate drift. The downstream terminal products include thin-film-transistor liquid crystal display panels, OLED backplanes, mini-LED driving backplanes, and projected capacitive touch sensor substrates.

    Silicon Trench Formation Using 5–25% TMAH Without Mobile Ion Contamination

    Micromachining of single-crystal silicon uses TMAH aqueous solutions as an anisotropic etchant where the absence of potassium is a hard requirement for subsequent integration with CMOS readout circuitry. The etch bath is formulated from 25 wt% electronic-grade TMAH diluted with ultrapure water to working concentrations between 5 wt% and 25 wt%; the chosen concentration is tied to desired etch rate, crystal-plane selectivity, and surface roughness. At 25 wt% and 80°C, the Si(100) etch rate is typically reported in the range of 0.5–1.0 µm/min; the exact rate depends on boron doping, dissolved oxygen, additive chemistry, and agitation. The process is run in PTFE or quartz tanks with reflux condensation, mechanical stirring or external recirculation, and temperature control within ±1°C. Masking is provided by LPCVD silicon nitride or thermal silicon dioxide; selectivity to thermal oxide is generally above 500:1 for 25 wt% TMAH at 80°C, though published data for device-specific configurations is limited. Because TMAH etch is sensitive to dissolved oxygen and silicate accumulation, the bath is periodically titrated with 0.1 N hydrochloric acid to maintain free hydroxide concentration, and nonvolatile solids are removed by filtration. The compliance anchor is SEMI C18 for the TMAH feed, which limits metal ions to levels that avoid shifts in the silicon etch rate and protect the final device from mobile ion contamination. Downstream production is used for bulk silicon diaphragm thinning, cavity formation, and through-feature definition in pressure sensors, accelerometers, gyroscopes, silicon microphones, inkjet printheads, microfluidic channels, and capillary structures for lab-on-chip devices.

    At production scale, etch-rate variation across a 150 mm or 200 mm silicon wafer is controlled by wafer boat design, bath agitation pattern, and vertical temperature profiling. Uncontrolled dissolved oxygen creates local etch-rate differences and increases pyramidal hillock density; nitrogen purging of the etch bath is therefore applied before wafer entry. Higher temperature operation at 90°C increases Si(100) etch rate but also accelerates water evaporation and shifts bath concentration, requiring automated conductance-based make-up dosing to keep TMAH concentration within the desired window. Published data for etch-rate anisotropy in production baths indicates that the (100):(111) etch-rate ratio can range from roughly 15:1 to 45:1 depending on concentration and additive load; this wide window is the key reason that a single TMAH etch recipe cannot be transferred across device designs without process revalidation.

    In wafer-level packaging lithography, TMAH developer is selected because it provides alkali-insensitive positive-tone resist development without introducing sodium or potassium into copper pillar, solder bump, or redistribution layer interfaces. The working concentration is generated by track-side dilution of 25 wt% TMAH stock to 2.38 wt% for standard packaging resists or to 1.19 wt% when thick positive DNQ-novolac resists require a reduced dissolution rate to preserve film-thickness loss. On production-scale automated spin coaters and developer tracks configured for 300 mm wafers or reconstituted panels, the development step uses multiple puddle cycles rather than a single spray, with total development time ranging from 90 s to 300 s for resist films between 20 µm and 100 µm. The dispense system is maintained as a single-pass point-of-use loop with 0.10 µm PTFE filtration and nitrogen blanketing; developer flow per nozzle is set between 1.0 L/min and 2.5 L/min to ensure adequate bulk turnover during dissolution of high resist loading. Compliance is anchored to SEMI C18 for metal cation limits, and contamination verification after under-bump metallization etch is performed by vapor-phase decomposition-droplet collection ICP-MS. The downstream wafer-level packaging process includes seed layer deposition, coating of thick photoresist, exposure on full-field steppers or mask aligners, development, oxygen plasma descum, Cu pillar electroplating, solder plating, photoresist stripping, and seed etch. Terminal outputs include copper pillar bumps, solder bumps, redistribution layers, through-silicon via liner redistribution, and fan-out wafer-level packages for mobile processors, power management integrated circuits, and radio-frequency components. Because thick-film development is mass-transport limited, the process window is narrower than front-end lithography; exhausted developer at the feature bottom creates footed profiles and variable sidewall angles, so puddle rotation and developer volume per wafer must be adjusted when feature aspect ratios exceed 1:1.

    When Fine-Line Semi-Additive Plating Resists Require Sodium-Free Development

    IC substrate and substrate-like PCB manufacturing uses TMAH developer for positive-tone liquid photoresists applied in semi-additive copper plating where fine-line capability below 10 µm line/space cannot tolerate sodium carbonate residue. The developer is prepared from 25 wt% TMAH stock diluted to 1.0–2.38 wt%, with the lower end of the range used for high-resolution liquid and dry-film resists that must retain a top surface loss of less than 0.5 µm during a 60–120 s development step. Purity is specified under SEMI C18 electronic-grade TMAH, and ionic cleanliness of the developed substrate is checked by IPC-TM-650 2.3.28 ion chromatography before electrolytic copper plating. Final substrate qualification follows IPC-6012 for rigid board reliability; the developer itself does not carry the compliance but must not introduce ionic contamination above specified extraction limits. The production process flows through material preparation, vacuum lamination or roller coating, exposure, development in horizontal inline chambers with spray and flood zones, deionized water rinse, oxygen plasma descum, electrolytic Cu plating, solder mask application, and final surface finish. The inline development equipment is configured with multiple spray manifolds and developer sump temperature control at 22–24°C; fresh TMAH developer is metered to maintain pH or conductivity setpoints because carbonate uptake and resist dissolution products reduce activity over continuous operation. Terminal products include fine-line package substrates, system-in-package modules, RF front-end modules, high-density interconnect boards, and chip-on-film substrates for display drivers. The operational boundary in this application is the reactive nature of TMAH toward certain flexible substrate adhesives and bare aluminum electrode layers; compatibility trials with production panels are required before changing developer normality or dwell time.

    TMAH application process matrix for Anji Microelectronics electronic-grade material
    Application segmentWorking concentrationOperating temperatureKey compliance or standardTerminal product types
    Advanced-node IC lithography2.38 ± 0.02 wt%23 ± 0.2°CSEMI C18; ISO 14644-1 Class 1–4Logic, DRAM, NAND, CMOS image sensors, analog/mixed-signal
    Flat panel display array development2.38 ± 0.03 wt%23 ± 1°CSEMI C18; ISO 14644-1 Class 4–6LCD, OLED backplane, mini-LED backplane, touch sensor
    MEMS silicon etching5–25 wt%70–90°CSEMI C18; PTFE or quartz vessel with ±1°C controlPressure sensors, accelerometers, gyroscopes, inkjet heads, microfluidics
    Wafer-level packaging lithography2.38 wt% or 1.19 wt%21–25°CSEMI C18; VPD-DC ICP-MS verificationCu pillar bumps, solder bumps, RDL, fan-out packages
    IC substrate and SLP development1.0–2.38 wt%22–24°CSEMI C18; IPC-TM-650 2.3.28Package substrates, SiP modules, RF front-end modules, HDI boards
    TMAH silicon anisotropic etch parameters for micromachining
    TMAH concentrationTemperatureApproximate Si(100) etch rateReported (100):(111) selectivity rangeProduction process notes
    5 wt%80°C0.4–0.6 µm/min15:1–30:1Surface roughness and hillock density depend on dissolved oxygen and additive package; full revalidation required for each device stack
    25 wt%80°C0.6–0.8 µm/min25:1–45:1Preferred when lower etch-rate variation is needed; nitrogen purging and filtration reduce silicate accumulation
    25 wt%90°C0.9–1.2 µm/min20:1–40:1Higher evaporation and concentration drift; automated conductance-based make-up dosing is required
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    Certification & Compliance
    More Introduction

    Tetramethylammonium hydroxide (CAS 75-59-2, molecular formula C4H13NO) supplied by Anji Microelectronics is an aqueous quaternary ammonium hydroxide used as a metal-ion-free photoresist developer, pH adjuster, and anisotropic silicon etchant in semiconductor and MEMS manufacturing. The product is classified by TMAH concentration and electronic-grade purity rather than by a single universal model code. Developer-grade material is supplied at nominal 2.38 wt% TMAH; etch-grade material is supplied at 25 wt% TMAH. Intermediate concentrations are produced for specific process integration. Lot-specific certificates of analysis accompany each batch and define the acceptance limits. Compared with industrial TMAH, the electronic-grade product is controlled for metallic cations, anions, particles, and carbonate species that affect lithography and etch uniformity.

    Physical property data for 2.38 wt% TMAH are close to water: density approximately 1.00 g/cm³ at 25°C, viscosity approximately 1.0 mPa·s at 25°C, and pH above 13. The 25 wt% etch grade has density approximately 1.02 g/cm³ at 25°C and pH above 14. These values are measured by density meter and pH electrode calibrated with traceable buffer solutions. The solutions are clear liquids ranging from colorless to faint yellow depending on concentration; color is not used as a purity indicator for electronic grade.

    Electronic-Grade TMAH Feedstock Characteristics and Anji Microelectronics Supply Positioning

    Electronic-grade TMAH from Anji Microelectronics is produced by purification sequences including multi-stage ion exchange and sub-µm filtration. The manufacturing path is selected to reduce metal-ion content below 1 ppb for individual transition metals; finished product is sampled and analyzed by inductively coupled plasma mass spectrometry. Anion burdens are controlled by ion chromatography. A representative specification envelope for semiconductor-grade TMAH of this class is given in the following table. Actual Anji lot acceptance limits may be tighter for specific process nodes and should be obtained from the vendor certificate of analysis.

    ParameterElectronic-grade control rangeAnalytical method
    TMAH concentration, developer grade2.38 ± 0.02 wt%Acid-base titration
    TMAH concentration, etch grade25.0 ± 0.5 wt%Acid-base titration
    Chloride50 ppbIon chromatography
    Sulfate50 ppbIon chromatography
    Phosphate20 ppbIon chromatography
    Sodium1 ppbICP-MS
    Potassium1 ppbICP-MS
    Calcium1 ppbICP-MS
    Iron1 ppbICP-MS
    Other transition metalseach ≤ 1 ppbICP-MS
    Total metals5 ppbICP-MS
    Particles ≥ 0.5 µm100 counts/mLLaser light scattering
    Carbonate as CO32−100 ppmIon chromatography or titration

    The supplied material is aligned to the analytical framework of SEMI C28 for tetramethylammonium hydroxide. Dilution and sample preparation for trace metal analysis use water conforming to ASTM D1193 Type I or ISO 3696 Grade 1. The absence of sodium and potassium in TMAH differentiates it from KOH and NaOH developers. In metal-oxide-semiconductor device fabrication, mobile alkali contamination above 1×1010 atoms/cm² at the gate oxide can induce threshold voltage drift; TMAH is therefore selected for post-gate development and cleaning operations where mobile ion residue cannot be tolerated.

    Why Does Developer Alkalinity Drift During Dilute TMAH Recirculation?

    In recirculating 2.38 wt% TMAH developer baths, hydroxide alkalinity is consumed by absorption of atmospheric CO2, forming tetramethylammonium carbonate and bicarbonate. Open baths can accumulate carbonate at levels exceeding 100 ppm within one shift, depending on bath surface area, air exchange, and drag-in. This changes the dissolution rate of positive-tone photoresist and can alter post-development critical dimension. Closed systems or nitrogen blanketing limit carbonate ingress. Point-of-use filtration at 0.05 µm removes agglomerated particles but does not remove dissolved carbonate. Conductivity and titration values therefore diverge as carbonate accumulates; titration remains the primary concentration control.

    Lithographic development with 2.38 wt% TMAH is performed on coater/developer tracks such as Tokyo Electron CLEAN TRACK ACT or SCREEN DUO series at 23 ± 0.5°C. Puddle times are typically between 30 s and 60 s for chemically amplified positive-tone resists. Exposed photoresist dissolves through acid deprotection and interaction with the developer, while unexposed regions remain hydrophobic and passivated. Track exhaust and chemical cabinet ventilation must be compatible with corrosive vapor. Development rate is monitored by optical endpoint or scatterometry on patterned wafers; linewidth shifts of ±2 nm can be induced by pH drift if carbonate is not controlled.

    TMAH developer is incompatible with exposed aluminum and with some low-k dielectrics under extended contact. The resist stack must cover aluminum pads and wafer edges where TMAH attack can generate hydrogen gas and roughness. TMAH should not be mixed with strong oxidizing acids. Published data for this specific configuration is limited, but standard operating practice avoids open-bath storage for more than 24 h without alkalinity titration and carbonate measurement.

    The difference between Anji-supplied TMAH and general industrial TMAH is primarily the electronic-grade impurity envelope rather than fundamental chemistry. Bulk industrial TMAH may be specified only by total alkalinity and color; cation burdens can be in the 10–100 ppb range or higher, and particle counts are not controlled for photolithography. Anji electronic-grade lots are released with ICP-MS cation data and particle counts, and are packaged in cleanroom containers under inert gas. The product also differs from KOH or NaOH etchants: KOH and NaOH introduce mobile alkali ions, whereas TMAH leaves no sodium or potassium cation residue after thermal processing. For post-etch cleaning, TMAH can replace solvent-based strippers only where polymer adhesion and swelling allow; it is not a direct solvent replacement for photoresist stripping without formulation adjustment.

    ParameterElectronic-grade TMAH developer 2.38 wt%Electronic-grade TMAH etchant 25 wt%Industrial TMAHKOH / NaOH
    Mobile alkali metal burden1 ppb per element1 ppb per element10–100 ppb or higherAlkali metal base
    Lithographic developer usePositive-tone DUV resist developmentNot used directly; dilutedNot suitable without purificationNot suitable due to metal contamination
    Silicon etch anisotropyNot typically used(100) silicon 0.3–1.0 µm/min at 70–90°CSimilar chemistry, inconsistent impuritiesSimilar etch, mobile ion contamination
    PackagingCleanroom, inert gas blanketedCleanroom, inert gas blanketedBulk containers, unspecified headspaceBulk containers
    Particle controlProcess-compatible, lot certifiedProcess-compatible, lot certifiedNot controlled for lithographyNot controlled for lithography

    When TMAH Is Used in Anisotropic Silicon Etch: Surface Roughness Constraints

    For bulk silicon micromachining, 25 wt% TMAH at 70–90°C etches (100) silicon at rates from 0.3 µm/min to 1.0 µm/min, with (110) etching faster and (111) etching significantly slower, providing crystallographic stop planes. Etch tanks are typically quartz or fluoropolymer with reflux condensation, temperature control of ±0.5°C, and agitation. Under these conditions, the etch rate of thermal silicon dioxide is low enough to give selectivity ratios exceeding 1000:1 for (100) silicon to thermal oxide, though the exact value depends on oxide quality, temperature, and carbonate contamination. Etch-generated hydrogen requires ventilation and exclusion of ignition sources.

    Surface roughness is influenced by TMAH concentration, temperature, and dissolved carbonate. Without roughness-control additives, anisotropic etching of (100) silicon in TMAH can produce pyramidal hillocks and RMS roughness values above 10 nm. Addition of non-ionic surfactant or silicate buffers can reduce RMS roughness to below 2 nm under optimized conditions. The Anji product is supplied without heavy-metal buffers, which preserves compatibility with CMOS front-end contamination budgets. Published data for this specific configuration is limited because roughness depends strongly on wafer source, masking material, and etch-loading ratio.

    Operational boundary: the etchant should not be used in stainless steel tanks because it is corrosive to aluminum, zinc, and some brass components. Equipment wetted surfaces are typically high-density polyethylene, polypropylene, PTFE, or quartz. Bath life is determined by carbonate buildup and etch-rate drift. In open systems at 80°C, evaporation must be replenished with deionized water, not fresh TMAH alone, to avoid concentration overshoot.

    Packaging for Anji TMAH is aligned to semiconductor chemical transport requirements. Typical containers are fluoropolymer-lined or acid-leached high-density polyethylene drums for 200 L volumes and canisters for 20 L point-of-use stations. Headspace is purged with nitrogen, and extraction ports are fitted with 0.05 µm PTFE filters to maintain particle cleanliness during chemical transfer. Before release, the material is tested for total alkalinity, density, viscosity, chloride, sulfate, phosphate, metal impurities, and particle count. A batch-specific certificate of analysis is provided. On-site incoming inspection typically confirms concentration by automatic potentiometric titration, particle count by laser scattering, and metal burden by ICP-MS after dilution in ASTM D1193 Type I water.

    What Limits TMAH Use in Post-CMP Cleaning and Ceria Slurry pH Adjustment?

    In copper barrier chemical mechanical planarization, TMAH is used as a hydroxide source for post-CMP cleaning formulations because it avoids alkali metal residues in narrow trenches. The usable concentration is limited by particle zeta potential shift. Excessive pH above 10 can alter dispersion stability of ceria or alumina abrasives, leading to sedimentation and defect formation. Formulators use zeta potential titration and particle size measurement to define the addition window. Filtration compatibility with PTFE or polypropylene elements is required. Anji TMAH can be blended with post-CMP cleaning concentrates, but blend stability must be validated on the target cleaning equipment because published data for this specific configuration is limited.

    The concentrated product is classified as corrosive under GHS and may carry hazard statement H314. Transport classification for the concentrated basic organic liquid is typically corrosive liquid, basic, organic, n.o.s., assigned under UN 3267. Storage should be between 15°C and 30°C in original containers with nitrogen headspace. Exposure to atmospheric CO2 during repackaging or sampling must be minimized. Waste neutralization is performed with dilute acid in a ventilated scrubber or approved chemical waste system because neutralization is exothermic and may release heat and vapor.

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