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Ascent Petrochem Holdings Co., Limited

Methylene Chloride Paint Stripper

    • Product Name: Methylene Chloride Paint Stripper
    • Factroy Site: Binhai New Area, Tianjin, China
    • Price Inquiry: sales4@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 673424
    Product Name Methylene Chloride Paint Stripper
    Active Ingredient Methylene chloride (dichloromethane)
    Chemical Family Chlorinated organic solvent
    Molecular Formula CH2Cl2
    Cas Number 75-09-2
    Appearance Clear to light yellow liquid
    Odor Sweet, chloroform-like odor
    Specific Gravity Density Approximately 1.33 g/cm³ at 20°C
    Boiling Point 39.8°C (103.6°F) for pure DCM; formulation boiling range typically 38–45°C
    Melting Point -96.7°C (-142.1°F)
    Vapor Pressure 350 mm Hg (46.6 kPa) at 20°C
    Vapor Density 2.93 (air = 1)
    Evaporation Rate 27.5 (butyl acetate = 1)
    Solubility Slightly soluble in water; miscible with many organic solvents
    Flash Point No flash point for pure methylene chloride; formulated parts may be combustible due to co-solvents
    Autoignition Temperature 556°C (1033°F)
    Flammability Limits In Air Approximately 13–22% by volume for pure DCM vapor
    Thermal Decomposition Products Hydrogen chloride, phosgene, carbon monoxide, and chlorine compounds when heated

    As an accredited Methylene Chloride Paint Stripper factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-gallon metal can with resealable lid, hazard labeling, and child-resistant closure for safe methylene chloride paint stripper storage.
    Container Loading (20′ FCL) 20′ FCL loaded with drummed methylene chloride paint stripper; secure, upright, segregated, with proper dangerous-goods labeling and ventilation.
    Shipping Ship methylene chloride paint stripper as UN1593 (Class 6.1, PG III) using certified, leak-proof containers. Ensure proper hazard labels, documentation, and corrosion-resistant packaging. Transport only via ground in well-ventilated areas, away from incompatible materials. Comply with all local, national, and international dangerous-goods regulations to ensure safe delivery.
    Storage Store methylene chloride paint stripper in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep containers tightly closed and upright, ideally in a corrosion-resistant, approved safety cabinet. Segregate from oxidizing agents, acids, and food items. Ensure spill containment and proper labeling to prevent accidental mixing.
    Shelf Life Shelf life is typically 2–3 years when stored sealed, cool, and dry; prevent evaporation and contamination.
    Application of Methylene Chloride Paint Stripper

    On flat-stock furniture panels where existing film build reaches 300–800 µm, methylene chloride stripping is used as a non-abrasive removal method because planing or sanding would reduce historical veneer thickness below 0.6 mm. The working formulation is typically compounded at 60–80% w/w methylene chloride, 8–15% w/w methanol as co-solvent, 1–2% w/w paraffin wax as evaporation retarder, and 0.5–1.5% w/w hydroxypropyl methylcellulose as thickener. Viscosity is maintained at 8,000–15,000 mPa·s measured on a Brookfield LVT spindle 4 at 30 rpm and 25 °C. The stripper is applied at 500–800 µm wet film thickness by flow-coat or solvent-resistant brush, then left under downdraft ventilation with a face velocity of 0.75 m/s. Nitrocellulose lacquer systems lift within 15–25 min; oil-modified alkyds require 30–45 min; two-component polyurethane clears with high crosslink density require 45–90 min. Removal is completed with a high-density polyethylene scraper or brass wool, never steel wool because iron particles embedded in wood grain later catalyse oxidative staining. Operators work under the exposure limits of 29 CFR 1910.1052, with breathing-zone samples held below the 25 ppm 8-h time-weighted average and the 125 ppm 15-min short-term exposure limit. Area-source facilities are subject to 40 CFR Part 63 Subpart HHHHHH. For hide-glue joints, polyethylene tape masks the glue line whenever dwell exceeds 45 min, because the methanol fraction can swell hide glue and reduce shear strength. After stripping, panels are conditioned at 21 °C ± 2 °C and 45–55% RH for 48 h before abrasive preparation to P180. The terminal substrate is raw wood with veneer thickness retained and no residual solvent odour, ready for sealing with dewaxed shellac or catalysed vinyl sanding sealer.

    Why Do Airframe Maintenance Manuals Specify Water-Rinsable Dichloromethane Strippers Before Recoating Alclad Surfaces?

    Mechanical abrasive stripping is restricted on Alclad 2024-T3 wing and fuselage skins because aggressive media remove up to 0.025 mm of cladding per pass and generate crevice corrosion sites. Water-rinsable dichloromethane strippers are therefore selected when the coating stack is 120–200 µm of polyurethane topcoat over epoxy primer. These formulations contain 70–80% w/w dichloromethane, 10–18% w/w methanol, 1.5–2.5% w/w paraffin wax, and 0.2–0.8% w/w acid inhibitor. Thickening to 12,000–18,000 mPa·s at 25 °C prevents flow off vertical stabilizer surfaces during 30–60 min dwell periods. Qualification is performed under ASTM F502-08 for effects on painted aircraft surfaces, and re-coated adhesion is checked under ASTM D3359-17. Spray application at 0.4–0.7 MPa is followed by high-pressure rinsing at 1,200–2,500 psi and 40–60 °C with deionized water below 10 µS/cm conductivity. The paraffin barrier slows evaporative weight loss by up to 40% in still air and ensures that the stripper remains active through the coating interface without over-wetting adjacent sealants. Residual wax on faying surfaces is measured by gravimetric wipe; values above 0.2 mg/ft² require an additional wipe with low-aromatic naphtha before primer. The process window is 18–30 °C; below 10 °C, the thickened film loses adhesion and removal rate drops sharply, while above 32 °C vapour generation exceeds engineering controls in open-bay operations. Titanium fasteners and magnesium alloy skins are isolated before application because dichloromethane residues can promote stress-corrosion cracking in Ti-6Al-4V under sustained tensile stress. After rinsing, the surface must be water break-free and is then dried with filtered compressed air at 2–3 bar. The terminal substrate is bare Alclad ready for chromate conversion coating per MIL-DTL-5541 Type II Class 1A, followed by epoxy primer per MIL-PRF-23377 and polyurethane topcoat per MIL-PRF-85285.

    Formulation variableBrush-gradeSpray-gradeImmersion-grade
    Dichloromethane70–75% w/w75–80% w/w65–70% w/w
    Methanol12–18% w/w10–15% w/w8–12% w/w
    Paraffin wax1.5–2.5% w/w1.0–2.0% w/w2.0–3.0% w/w
    Thickener1.0–2.0% w/w0.5–1.0% w/w0.8–1.5% w/w
    Viscosity at 25 °C14,000–18,000 mPa·s10,000–14,000 mPa·s12,000–16,000 mPa·s

    Because methylene chloride diffuses through aged OEM polyurethane within 20–40 min at 20 °C, automotive restoration lines reserve it for steel body shells, hinges, and bumper brackets rather than complete vehicle immersion. The formulations applied to cold-rolled E-coated steel are built around 70–85% w/w methylene chloride, 10–20% w/w aliphatic hydrocarbon, 1–3% w/w paraffin wax, and 0.5–2% w/w methanol. Viscosity is controlled between 10,000 and 20,000 mPa·s so that vertical door frames hold a 1.0–1.5 mm wet film without sagging. Dipping tanks are constructed from 316L stainless steel with 20 mm water seal and refrigeration coils holding the bath at 18–22 °C. Acrylic lacquer primer lifts in 20–30 min; epoxy primer and electrocoat require 30–50 min; aged moisture-cured urethane on truck frames may need two applications and 90–120 min. After removal, panels are rinsed with 60 °C water at 80–120 bar, and rinse-water conductivity is held below 20 µS/cm to prevent chloride pitting in deep-drawn zones. Body filler must be mechanically removed before stripper contact because polyester putty degrades into a porous residue that traps solvent and later lifts the repaint system. Zinc-coated panels receive a pH-neutral rinse and are moved to phosphate within 4 h; red rust appears earlier on bare cold-rolled surfaces if relative humidity exceeds 60% RH. Exposure monitoring follows 29 CFR 1910.1052(c), and all dip-tank exhaust slots maintain 0.5 m/s capture velocity. The terminal output is a dry steel substrate with no visible coating film, ready for zinc phosphate conversion and cathodic electrocoat without hand sanding.

    Shipyard Hull Block Stripping and Chloride-Induced Pitting Control on A36 Steel

    Shipyard block stripping uses methylene chloride where dry abrasive blasting is prohibited by adjacent hot-work permit conditions or where dimensional tolerances on thin plate below 5 mm must be preserved. The coating stack is typically 400–1,200 µm of epoxy anticorrosive, polyurethane intermediate, and self-polishing antifouling, and the stripper is formulated with 60–75% w/w dichloromethane, 5–10% w/w methanol, 2–4% w/w paraffin wax, and 0.5–1.0% w/w amine-carboxylate corrosion inhibitor. Viscosity is thixotropic at 4,000–8,000 mPa·s after shearing through a 45:1 airless pump at 0.5–0.8 MPa with a reversible-clean tip. The material is sprayed at 500–1,000 µm wet film, covered with polyethylene sheet, and left for 90–180 min; high-build epoxy requires reapplication after mechanical removal of the first lifted layer. Stripped coating mass is removed with fresh water at 1,500–2,500 psi and 40 °C, followed by a low-pressure detergent wash. Because dichloromethane residues mixed with hygroscopic salts can initiate pitting on A36 steel, soluble-salt testing is conducted with the Bresle patch method under ISO 8502-6. For immersion-service tanks, chloride ion loading must be below 50 mg/m² as NaCl; for atmospheric hull sides, 100 mg/m² is the upper limit. Zinc sacrificial anodes are removed or masked before stripping because the stripper’s hydrolysis products accelerate anode consumption and leave sludge on the steel surface. When the chloride threshold is exceeded, secondary dry abrasive blasting to ISO 8501-1 Sa2½ is mandatory before priming. The terminal substrate is a uniformly abraded hull block with an anchor profile of 25–40 µm, suitable for zinc silicate shop primer and subsequent epoxy holding primer in newbuilding or repair programmes.

    When Cured Coating on Plating Racks Exceeds 1,000 µm, Alkaline Immersion Is Replaced by Cold Dichloromethane

    Electroplating racks coated with epoxy-polyester powder gradually accumulate 800–1,500 µm of cured film at copper hooks and stainless contact points. Hot alkaline immersion strips the outer film but leaves an insoluble crosslinked underlayer that reduces electrical contact and alters rack geometry. Cold methylene chloride immersion at 18–25 °C lifts this material from steel hooks; published laboratory data for thick epoxy-polyester powder films are limited, so production tanks determine endpoint by visual lifting at the hook radius, with immersion timers set at 3–6 h depending on film thickness and ventilation limits. The working bath contains 80–85% w/w methylene chloride, 5–8% w/w methanol, 3–5% w/w paraffin wax, and 0.5–2% w/w ethoxylated surfactant. The tank body is 316L, sealed by a 20 mm water layer, fitted with refrigeration coils holding 18–22 °C, and vented at 0.5 m/s rim capture. Racks are loaded on a programme hoist with a drain time of 15 min, then rinsed at 50–80 bar with municipal water below 25 °C. PVC plastisol-coated racks are not suitable for this bath because dichloromethane swells plastisol by more than 8% by volume within 24 h and causes delamination. Operators sample the liquid phase for paraffin buildup every 40 batch hours; when paraffin exceeds 6% w/w, skimming is performed. Air monitoring follows 29 CFR 1910.1052(c), and exhaust stacks require carbon adsorption or incineration under 40 CFR Part 63 Subpart HHHHHH where applicable. The terminal product is a stripped rack with bright steel hooks and no residue at contact points, ready for re-coating or immediate return to the plating line.

    Control parameterSet pointInspection method
    Liquid temperature18–22 °CCalibrated resistance thermometer
    Bath moisture0.1–0.3% w/wKarl Fischer titration
    Vapour concentration<25 ppmPhotoionization detector with 10.6 eV lamp
    Immersion time3–6 hProgramme hoist log
    Rinse pressure50–80 barCalibrated pressure gauge at nozzle

    Cast-iron restoration differs from millwork stripping in that the methylene chloride gel is applied over intact 100–200 µm alkyd films on architectural metal rather than on exposed wood fibres. The gel poultice is compounded with 50–60% w/w methylene chloride, 5–8% w/w methanol, 3–5% w/w paraffin wax, and 3–5% w/w fumed silica, producing a yield stress that holds a 1.5–2.0 mm layer on vertical bronze doors and radiator castings without sag. The poultice is applied with a stainless steel straight-edge, then covered with 0.025 mm polyethylene film to slow solvent loss. Dwell is 45–90 min for alkyd enamel and 90–120 min for lead-containing primer on cast iron; on bronze, dwell is capped at 60 min to avoid surface dezincification in polished zones. Lifted paint is removed with phenolic or nylon scrapers, and residual stripper is neutralized with mineral spirits followed by a dilute alkaline wash at pH 8.5–9.5. Cast iron is then passivated with 5% w/w phosphoric acid at pH 1.8, rinsed, and force-dried with low-pressure air at 2–3 bar. Lead paint removal on pre-1978 buildings requires compliance with 40 CFR Part 745 Subpart E, including HEPA-filtered shrouds and waste characterization under 40 CFR Part 261. The terminal product is an architecturally clean casting with a uniform grey substrate, primed within 4 h with a zinc-rich or epoxy mastic primer to prevent flash rust.

    Paint-Robot Bell Cup Decontamination with Paraffin-Sealed Dichloromethane Gels

    Bell cups and electrostatic ring nozzles on high-speed paint robots accumulate flash-cured two-component urethane at internal radii where mechanical reaming changes diametrical clearance by more than 0.02 mm. Paraffin-sealed dichloromethane gel is introduced into the disassembled cup channel at 65% w/w dichloromethane, 15% w/w methanol, 5% w/w paraffin wax, and 1% w/w non-ionic fluorosurfactant, thickened to 18,000–25,000 mPa·s. The parts are placed in a sealed ultrasonic tank operating at 25 kHz and 60 W/L, with the cleaning solution held at 20–22 °C for 10–30 min. The paraffin phase forms a temporary film that limits evaporation during ultrasonic degassing and prevents chloride attack on 17-4 PH stainless components. After removal, parts are drained for 5 min, rinsed with 99% isopropanol, then dried with filtered compressed air at 2 bar. Polycarbonate laser window covers and Buna-N O-rings must be removed before exposure because dichloromethane stress-crazes polycarbonate within 5 min and increases Buna-N volume swell beyond 25% in 1 h. Explosion-proof electrical equipment is selected under ATEX Directive 2014/34/EU, and the cleaning cell is interlocked with a flammable-gas detector at 10% LEL. The terminal product is a dimensionally unchanged bell cup with no retained paint solids in the circumferential feed channel and no chloride residue on electrostatic surfaces.

    Supplied in bulk, 25 kg drums and 200 L steel drums. We provide import‑export service for global customers. Please contact us for latest price.

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    Certification & Compliance
    More Introduction

    Designated DCM-PS 99.9, the methylene chloride paint stripper is supplied as a low-methanol, epoxide-stabilized solvent blend formulated for cold immersion, flow-on, and brush application on steel, stainless steel, and concrete. The active solvent is dichloromethane, CAS 75-09-2, at ≥99.0 wt%; the product has a boiling point of 39.6 °C at 101.3 kPa, a liquid density of 1.32 g/cm³ at 20 °C, and a vapor pressure of 47 kPa at 20 °C. The stabilizer package is intended to maintain acid acceptance sufficient to keep recovered solvent non-corrosive to 316L stainless steel immersion racks, while the low-methanol composition reduces phase separation when water is used as a bath cap. The product is non-flammable under closed-cup testing but may generate acidic decomposition products if vapor is exposed to hot surfaces.

    ParameterMethodSpecification
    Dichloromethane contentGas chromatography, internal standard≥99.0 wt%
    Distillation rangeASTM D107839.0–40.5 °C at 101.3 kPa
    Density at 20 °CASTM D40521.320–1.330 g/cm³
    Closed-cup flash pointASTM D93No flash point
    Water contentASTM D1364≤0.02 wt%
    Vapor pressure at 20 °CASTM D287946–48 kPa

    At 20 °C the dynamic viscosity is approximately 0.42 mPa·s, which permits penetration into weld seams, bolt threads, and narrow flanges without thickening agents. Because the formulation does not contain paraffin wax or aromatic hydrocarbons, it leaves no waxy film after high-pressure rinse. That property is significant when subsequent phosphate conversion coating or powder primer adhesion is specified according to ASTM D3359. The product is supplied in 205 L 316L stainless steel or phenolic-lined steel drums with nitrogen headspace at 10–20 kPa gauge. Bulk deliveries use 20,000 L stainless steel tank trailers with a top-pad water layer to reduce vapor loss. Shelf life is 24 months when stored at 5–30 °C away from direct sunlight.

    Film thickness effects are non-linear. A 25 µm alkyd topcoat may lift in 5–12 min, whereas a 250 µm multi-coat system may require 45–90 min at 20 °C, depending on crosslink density and pigment volume concentration. Epoxy primers with high barium sulfate loading often resist initial swelling; mechanical scoring or brush agitation after 15 min increases solvent ingress by disrupting the pigment-rich surface skin. These dwell ranges are inspection-based and should be revalidated when coating source or cure history changes.

    What Distinguishes a Stabilized Dichloromethane Stripper from NMP, DBE, and Benzyl Alcohol Alternatives?

    Compared with N-methyl-2-pyrrolidone, dibasic ester, and benzyl alcohol formulations, the dichloromethane product operates by rapid solvent diffusion into the polymer film rather than by hydrolysis or slow ester swelling. The Hildebrand solubility parameter of dichloromethane is 19.8 MPa1/2, which places it within the solubility window of many air-dried alkyd, epoxy, and chlorinated rubber binders. In comparative immersion testing using 100 µm aged alkyd panels at 20 °C, DCM-PS 99.9 lifts the film in 10–30 min, while NMP and DBE formulations require 2–24 h under the same conditions. Benzyl alcohol strippers typically require alkaline co-activators and show slower penetration into crosslinked epoxy; DBE and benzyl alcohol also leave high-boiling residues that can interfere with subsequent phosphate conversion coating or powder topcoat adhesion.

    AttributeDCM-PS 99.9NMP-basedDBE-basedBenzyl alcohol-based
    Dwell time to lift 100 µm aged alkyd at 20 °C10–30 min2–24 h6–24 h4–12 h
    Boiling point39.6 °C202 °C196–215 °C205 °C
    Closed-cup flash pointNo flash point, ASTM D9386 °C, ASTM D93>100 °C, ASTM D93101 °C, ASTM D93
    Residue tendency after rinseLow; no waxy filmModerate; solvent retention possibleHigh; oily ester residueModerate; aromatic alcohol residue

    The product also differs from hot alkaline strippers in that it is non-alkaline and does not saponify oil-based binders; it relies on solvation. Hot alkaline strippers may generate hydrogen gas on aluminum and can cause caustic stress corrosion cracking on certain stainless steels. DCM-PS 99.9 introduces no alkaline residue, but it is not the correct selection for highly crosslinked thermoset powder epoxies because high crosslink density limits solvent swelling; mechanical or thermal stripping is typically required for those films.

    Cold immersion is conducted in a covered polypropylene or 316L stainless steel tank with a water cap of 1–2 cm to reduce headspace dichloromethane concentration. The bath temperature is maintained at 18–25 °C; above 30 °C, vapor loss accelerates and the workplace exposure limit of 25 ppm 8-hour TWA under OSHA 29 CFR 1910.1052 becomes difficult to control without slot hoods capturing at 45–60 m/min face velocity. Workpieces with multi-coat epoxy up to 250 µm are immersed 15–45 min, then removed and rinsed with high-pressure water at 35–70 bar and 40–55 °C. Sludge containing swollen coating solids should be removed from the tank bottom at intervals no longer than 72 h to prevent accumulation of chlorinated acids at the water-solvent interface.

    Immersion-Stripping Control Parameters for Multi-Coat Alkyd Systems

    Effective stripping of multi-coat alkyd systems requires control of solvent activity rather than simple extension of dwell time. At 20 °C, the product swells plasticized alkyd binder quickly; beyond 45 min, the rate becomes limited by solvent transport through the swollen polymer shell. Bath agitation at 0.3–0.6 m/s linear flow, produced by a corrosion-resistant centrifugal pump with a 316L stainless steel casing, removes the saturated boundary layer and reduces dwell-time variance between high- and low-rack positions. Water content should be held at <0.2 wt% because higher moisture displaces solvent from the polymer interface and produces blister-like lifting on epoxy primers. The pH of the water cap is maintained between 6.0 and 7.5; alkaline pH above 8.0 accelerates dichloromethane dehydrochlorination and can increase free chloride in the bath, which contributes to pitting on 316L stainless steel racks at weld seams.

    Production-scale immersion lines without external cooling frequently show the most severe process drift when coated steel components are transferred directly from a hot curing oven into the stripper. The accumulated heat can raise the bath above 30 °C within 30 min, creating a processing threshold at which headspace vapor concentration may no longer remain below the OSHA action level of 12.5 ppm if local ventilation is marginal. Jacketed cooling or an external plate heat exchanger with 316L wetted parts is specified for continuous operation to hold the bath at 18–25 °C. Published line-specific performance data for this configuration is limited; however, the temperature control requirement is derived from the vapor pressure curve of dichloromethane and from workplace exposure limits rather than from product-specific testing alone.

    When Methylene Chloride Paint Stripper Replaces Mechanical Blasting on Thin-Gauge Stainless Steel

    Mechanical blasting on thin-gauge 304 stainless steel can induce surface stress and unacceptable warpage; solvent stripping is specified where dimensional tolerance and surface finish must be preserved. DCM-PS 99.9 removes alkyd and epoxy coatings without altering the 2B mill finish, provided that post-rinse chloride inspection is performed according to ISO 8502-5 and the surface is dried within 30 min. Unlike abrasive blasting, the product does not remove mill scale, weld spatter, or provide an angular anchor profile. If the subsequent coating system requires a 25–50 µm surface profile for adhesion, mechanical blasting remains necessary. This product is therefore selected only when surface contamination and dimensional stability are the controlling factors.

    The product falls under OSHA 29 CFR 1910.1052 occupational exposure requirements: the 8-hour time-weighted permissible exposure limit is 25 ppm, the action level is 12.5 ppm, and the 15-minute short-term exposure limit is 125 ppm. In the EU, placing on the market as a paint stripper for general consumer use is restricted under REACH Annex XVII Entry 59; industrial use requires closed-system controls or local exhaust ventilation consistent with workplace chemical safety requirements. The product is not recommended for magnesium, zinc, titanium, or unsealed aluminum components in continuous immersion because chlorinated solvent-metal contact can generate local hydrogen chloride and pit the substrate. Nitrile and latex gloves show short breakthrough times; glove selection should follow ASTM F739 permeation data supplied by the glove manufacturer. Strong aqueous caustic and amine-based epoxy hardeners should be kept out of the bath because dehydrochlorination can generate heat and acidic decomposition products.