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KLJ Plasticizers Kanatol 100 Dimethyl Phthalate (DMP)

    • Product Name: KLJ Plasticizers Kanatol 100 Dimethyl Phthalate (DMP)
    • Factroy Site: Jiangjun Avenue 55#, Jiangning Area, Nanjing, China
    • Price Inquiry: sales7@alchemist-chem.com
    • Manufacturer: Alchemist Worldwide Ltd
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    Specifications
    HS Code 266248
    Product Name KLJ Plasticizers Kanatol 100 Dimethyl Phthalate (DMP)
    Chemical Name Dimethyl phthalate
    Cas Number 131-11-3
    Einecs Number 205-011-6
    Molecular Formula C10H10O4
    Molecular Weight 194.18 g/mol
    Appearance Clear, colorless, oily liquid
    Odor Slight aromatic odor
    Density 1.19 g/cm³ at 20 °C
    Specific Gravity 1.190-1.194 at 20/20 °C
    Boiling Point 282-284 °C at 760 mmHg
    Melting Point 2 °C
    Freezing Point 0 °C
    Flash Point 146 °C (closed cup)
    Refractive Index 1.5155 at 20 °C
    Viscosity 17.2 mPa·s at 20 °C
    Water Solubility 4.0 g/L at 25 °C
    Vapor Pressure 0.01 mmHg at 20 °C
    Purity ≥99.5%
    Acidity ≤0.01% as phthalic acid
    Moisture ≤0.1%
    Color ≤30 APHA

    As an accredited KLJ Plasticizers Kanatol 100 Dimethyl Phthalate (DMP) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of KLJ Plasticizers Kanatol 100 Dimethyl Phthalate (DMP)

    Cellulose acetate sheet and profile extrusion integrates Kanatol 100 DMP as a primary plasticiser at 18–25 phr, calculated on dry cellulose acetate flake. The plasticiser is absorbed in a jacketed high-speed mixer at 110–125 °C before the dry blend is transferred to a vented single-screw extruder with L/D 25:1 to 30:1 and a chromium-plated screw. A breaker plate carrying wire screens of 150–250 µm is installed ahead of the die; barrel temperatures are profiled from 160 °C in the feed zone to 215 °C in the metering zone, with vacuum degassing at 0.08–0.09 MPa to strip residual water and entrained air. The melt is formed into sheet or profile through a flat die or calibration sleeve, then polished on a three-roll stack with roll temperatures from 70 °C to 110 °C. Finished sheet thickness typically ranges from 0.3 mm to 4.0 mm. The presence of DMP reduces melt viscosity and permits lower melt temperatures than unplasticised cellulose acetate; however, because the boiling point of DMP is 284 °C, melt zones maintained above 220 °C increase the rate of volatilisation and produce surface splay on the extrudate. Tensile properties of the plasticised sheet are checked under ASTM D638-14, flexural modulus under ISO 178:2019, and Vicat softening temperature under ISO 306:2022. If the sheet is intended for secondary fabrication, drilling and routing coolant must not exceed 40 °C to avoid localised plasticiser migration. End products include spectacle frames, tool handles, display packaging, and decorative automotive interior trim. No food-contact claim is assigned to this application unless the specific finished article is assessed under current Commission Regulation (EU) 10/2011 migration rules.

    How Dimethyl Phthalate Shifts Nitrocellulose Lacquer Hardness and Adhesion

    Nitrocellulose nail enamel and clear wood lacquer manufacture introduces Kanatol 100 DMP after the nitrocellulose flake has been wetted with ethyl acetate or butyl acetate. The addition level is 10–30 parts DMP per 100 parts dry nitrocellulose, and the plasticiser is frequently split with camphor or a short-chain polyester plasticiser when higher surface hardness is demanded. Mixing is carried out in a cooled stainless steel vessel with a Cowles disperser at 600–900 rpm; jacket temperature is maintained below 35 °C because solvent vapour from the lacquer is flammable. The DMP addition reduces the modulus of the dried film and improves its cold flex resistance. For nail enamel, the finished lacquer is filled into cap brush bottles and stabilised at 20–25 °C for 24 h before batch release. Film adhesion on cellulose propionate display panels is tested by cross-cut tape pull under ASTM D3359-17, and pendulum damping hardness is measured under ISO 1522:2022. DMP is not included in the current harmonised list of CMR substances under CLP Regulation (EC) No 1272/2008; nevertheless, the finished cosmetic product must be supported by a product information file under EU Regulation 1223/2009, and residual solvent and plasticiser exposure must be addressed in the safety dossier. In wood lacquers applied at 100–150 g/m² wet film weight, the dry film is sanded after 24 h and recoatability is checked after a 72 h interval. Excess DMP above 30 parts per hundred nitrocellulose produces a tacky film at 25 °C and retards lacquer print hardness; upper limits are therefore set by pendulum damping acceptance criteria rather than by a fixed addition limit.

    Downstream segmentRelevant standard or directiveParameter or condition tracked
    Cellulose acetate sheet extrusionASTM D638-14, ISO 306:2022Tensile modulus, elongation, Vicat softening
    Nitrocellulose nail enamelEU 1223/2009, ISO 1522:2022Cosmetic product safety dossier, pendulum damping hardness
    Flexographic and gravure inksISO 2431:2019, ASTM D3359-17Flow cup viscosity, tape adhesion after solvent release
    High-solids alkyd enamelsASTM D1640-14, EU 2004/42/ECDrying time, volatile organic compound limit
    Nitrile and chloroprene rubberISO 6502:2018, ASTM D412-16Cure rheometry, tensile stress-strain
    Fine fragrance concentrateEU 1223/2009, ASTM D4052-18Cosmetic safety dossier, density quality check

    For flexographic and gravure ink systems, Kanatol 100 DMP functions as a plasticising cosolvent and resin-solvency modifier at 2–8 wt% of the liquid ink. The pigment dispersion pass is carried out in a horizontal bead mill charged with 0.6–0.8 mm yttria-stabilised zirconia beads, with the milling chamber held at 40–45 °C; DMP is post-added during the letdown phase under low shear to avoid viscosity instability at the mill outlet. In nitrocellulose and polyamide lamination inks printed on treated polyethylene and polyethylene terephthalate, the ester slows solvent release during the drying tunnel and improves film recoatability on central impression presses operating at 250–400 m/min. Too high a DMP concentration above 8 wt% delays solvent release sufficiently to cause blocking at rewind tension settings from 120–180 N/m, and the printed roll then exhibits transfer marking. Ink viscosity is checked on a flow cup according to ISO 2431:2019, and adhesion of the printed film is assessed by a tape test under ASTM D3359-17. Packaging ink formulations are screened against REACH Annex XVII and, where food-contact printed matter is produced, against the relevant national food-contact legislation because the ink is not a direct food-contact layer. End products include reverse-printed snack packaging, self-adhesive labels, and shrink-sleeve films. The use of DMP in this segment is limited to solvent-based ink systems; its solvency is insufficient for waterborne polyurethane dispersions.

    When a Low-Odour Coalescing Plasticiser Is Required in High-Solids Alkyd Enamels

    Industrial alkyd enamel and metal primer manufacture incorporates Kanatol 100 DMP during the letdown phase at 2–5 wt% based on alkyd resin solids. The addition is made after the mill base has been cooled below 50 °C because DMP exposure to the highest disperser shear can temporarily raise the mill-base temperature and increase volatilisation. Pigment wetting is carried out on a high-speed disperser at 10–15 m/s tip speed, followed by bead milling; the DMP is then introduced under low shear with a pitched-blade stirrer at 200–300 rpm. DMP remains in the film during forced drying because its boiling point is 284 °C, and it reduces internal stress in films applied to grit-blasted steel at 50–80 µm dry film thickness. Drying time is measured under ASTM D1640-14, pull-off adhesion under ASTM D4541-17, and VOC content is controlled under EU Directive 2004/42/EC for the relevant product category. At additions above 5 wt%, through-dry is retarded because the phthalate remains mobile in the ambient-cured film; recoating intervals must then be extended beyond the standard 24 h window. End products include metal furniture enamels, agricultural equipment primers, and anti-corrosive maintenance coatings. DMP is not a reactive diluent in this application; it does not enter the oxidative cross-linking of the alkyd network, and its use is therefore bounded by tensile elongation requirements rather than by cure speed.

    Nitrile rubber and chloroprene rubber compounds use Kanatol 100 DMP as a polar plasticiser at 5–15 phr, typically added after carbon black and silica dispersion in the second pass of an internal mixer. The ram pressure is maintained at 0.4–0.6 MPa, and the dump temperature is held below 120 °C because DMP vapour is detected in the extraction ductwork when the batch temperature is allowed to rise. Two-roll mill sheeting follows at 50–60 °C roll temperature; the plasticiser improves banding and reduces edge tearing on high-hardness NBR compounds. Cure data are collected on a moving-die rheometer at 160 °C according to ISO 6502:2018, while tensile sheets are cured and tested under ASTM D412-16. DMP lowers compound viscosity but does not function as a rubber process oil for highly extended compounds; increasing the plasticiser above 15 phr increases volatility loss during hot air ageing at 100 °C and lowers Shore A hardness in a nonlinear manner. The main end products are oil-resistant gaskets, fuel-cell gaskets, and hydraulic seal preforms. Compounds containing DMP should not be subjected to continuous service above 100 °C without post-cure volatile-loss evaluation, and their extraction resistance is lower than that of polymeric plasticisers in IRM 903 oil.

    Fragrance Fixative Use in Ethanol-Based Fine Perfume Concentrates

    In fine fragrance compounding, Kanatol 100 DMP is incorporated as a high-boiling solvent and fixative at 1–10 wt% of the perfume oil concentrate. The concentrate is blended in a stainless steel vessel at 20–23 °C with a gradual addition sequence to avoid local precipitation of lipophilic raw materials. After dissolution, the solution is filtered through a 0.45 µm membrane cartridge and density is checked at 20 °C against 1.19 g/cm³. Refractive index is checked against 1.5138 at 20 °C, and these two values serve as release benchmarks under ASTM D4052-18 and ISO 280:1998. The flash point of DMP is 146 °C, so the concentrate is not classified as a flammable liquid under standard GHS flash point criteria. The finished perfume product must be assessed under EU Cosmetic Regulation 1223/2009; DMP is not listed in Annex II as a prohibited substance, but the product information file must address skin-contact exposure by quantitative batch calculation. The usage level is limited by fragrance house IFRA Standards where applicable and by the desired degree of retentivity on skin. DMP is less volatile than ethanol, so it remains in the dried fragrance film and modulates the evaporation curve of top-note components. End products include eau de toilette, aftershave, and scented body sprays. Published data for DMP-specific fixative retention in fine fragrance is limited; headspace GC-MS comparison against an internally validated reference blend is used to compare emission profiles on a batch-specific basis.

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    Certification & Compliance
    More Introduction

    KLJ Plasticizers Kanatol 100 is a commercial dimethyl phthalate (DMP) ester whose principal constituent is dimethyl benzene-1,2-dicarboxylate, CAS 131-11-3, molecular formula C10H10O4, and molar mass 194.18 g/mol. The product is manufactured by methanol esterification of phthalic anhydride and is supplied as a clear liquid with an ester content not less than 99.0 % w/w, acidity no greater than 0.02 % w/w as phthalic acid, and moisture no greater than 0.10 % w/w by Karl Fischer titration. Density at 27 °C is specified between 1.188 g/cm³ and 1.195 g/cm³, refractive index at 27 °C is 1.513–1.515, and dynamic viscosity at 25 °C is approximately 17.2 mPa·s. Boiling point at atmospheric pressure is 283.7 °C, melting point approximately 2 °C, and closed-cup flash point approximately 146 °C. Water solubility is below 0.5 % w/w at 20 °C; the ester is miscible with alcohols, ketones, esters, glycol ethers, and aromatic hydrocarbon solvents. Release parameters are monitored by colour per ASTM D1209, density per ASTM D4052, acid number and moisture per ASTM D1045, and refractive index per ASTM D1218.

    Why Dimethyl Phthalate Behaves as a High-Solvating, Low-Molecular-Weight Plasticizer

    The ortho-diester arrangement in DMP creates a compact polar molecule that disrupts interchain hydrogen bonding in cellulose nitrate, cellulose acetate, and cellulose acetate butyrate more effectively per unit mass than higher-molecular-weight phthalate esters. Because the molar mass of DMP is lower than that of diethyl phthalate and dibutyl phthalate, equal mass loadings introduce a greater molar quantity of plasticizer and typically produce faster viscosity reduction in high-solids lacquer systems. However, the compact molecular structure also raises vapour pressure relative to general-purpose phthalates, which limits permanence in open film or coating applications. Comparative data for homologous ortho-phthalate esters are summarised in Table 1.

    Table 1. Comparative typical properties of dimethyl phthalate and reference ortho-phthalate esters
    PropertyKanatol 100 (DMP)Diethyl phthalateDibutyl phthalate
    Molar mass, g/mol194.18222.24278.34
    Boiling point at 101.3 kPa, °C283.7295340
    Density at 20 °C, g/cm³1.191.121.05
    Dynamic viscosity at 25 °C, mPa·s17.210.516.6
    Water solubility at 20 °C, g/L4.31.00.01
    Closed-cup flash point, °C146160171

    Hansen solubility parameter data reported in solvent databases place DMP close to the polar solubility region required for nitrocellulose and cellulose ester resins. This explains why lower DMP loadings can replace higher loadings of dibutyl phthalate in certain lacquer concentrates, although the exact replacement ratio depends on the solvent blend, resin nitrogen content, and final film hardness target. Published data for this specific formulation configuration are limited, so production trials with viscosity and gloss control are used to establish the substitution ratio.

    Processing Boundaries in Cellulose Ester and Vinyl Resin Compounding

    Across production compounding and film-casting lines, the primary constraint on DMP is volatility under sustained heat. Volatility tests conducted according to ASTM D2288 at 155 °C for 24 h show higher mass loss for dimethyl phthalate than for dibutyl phthalate and substantially higher loss than for high-molecular-weight general-purpose phthalates. Closed mixing vessels, chilled vent condensers, and local exhaust ventilation are specified when DMP is processed in open mills or heated dispersion tanks above 120 °C. In extrusion operations using counter-rotating twin-screw machines with L/D ratios from 30:1 to 40:1, DMP is not used as the primary plasticizer because barrel zones above 150 °C generate vapour that can condense on feed-throat surfaces and initiate bridging. Vented barrels with vacuum extraction and condensation traps are required if partial replacement is attempted. The closed-cup flash point of approximately 146 °C also places the product in a flammable liquid classification under common storage and handling codes; heating systems must maintain headspace temperatures below the lower explosive limit and avoid exposed electrical elements.

    In cellulose nitrate lacquers for wood and metal substrates, Kanatol 100 is metered into solvent-based formulations at loadings commonly between 5 phr and 15 phr on dry binder. Spray viscosity is adjusted to 18–25 s in a DIN 53211 flow cup at 20 °C; addition of DMP at the lower end of the loading range provides high-solids viscosity control while retaining gloss and block resistance. In cellulose acetate film casting, DMP is blended into acetone-based dope before casting onto polished stainless steel belts. Tensile properties of the finished film are evaluated according to ASTM D882, and elongation at break increases while tensile strength decreases as DMP loading increases. Because DMP is partially water-soluble, cast films exposed to relative humidity above 60 % can show surface tack or whitening; formulations for humid service are adjusted by partial substitution with more hydrophobic plasticizers.

    When DMP Replaces Dibutyl Phthalate in PVC Plastisol and Organosol Systems

    When Kanatol 100 is introduced as a partial replacement for dibutyl phthalate in PVC organosol or spread-coating formulations, three measurable differences appear. First, paste viscosity at equal plasticizer mass is lower immediately after mixing, but the rate of viscosity increase over 24 h is higher because DMP solvates PVC particles more rapidly. Second, gelation and fusion temperatures are reduced, which can shorten oven dwell time in spread-coating lines; however, the processing window narrows because DMP volatility increases near 150 °C. Third, because DMP is more polar and has a different solubility parameter than dibutyl phthalate, tensile strength and elongation do not track linearly with DBP replacement; formulators re-optimize filler content and stabilizer package when the substitution is made. These differences are quantified by dynamic mechanical analysis at 1 Hz under ISO 6721 and by tensile testing under ISO 527-2. Formulations intended for automotive or appliance coatings therefore limit DMP to 5–10 phr and supplement permanence with a higher-molecular-weight plasticizer.

    Addition of Kanatol 100 to suspension-grade PVC plastisols produces a rapid reduction in paste viscosity at loadings of 5–10 phr when measured by Brookfield viscometry at 20 rpm and 25 °C. The same solvating activity accelerates room-temperature gelation and can increase plastisol viscosity during storage. Accelerated storage at 40 °C for 7 days typically shows a greater viscosity rise with DMP than with di-2-ethylhexyl phthalate at equal phr. Fusion behaviour is monitored by heating a plastisol film on a Kofler bench or in a forced-air oven, and the transition from paste to clear fused film occurs at a lower temperature when DMP replaces a portion of the general-purpose plasticizer. Tensile properties of fused sheets are determined according to ISO 527-2, hardness according to ISO 868, and chemical resistance according to ISO 175. Because DMP is more extractable in water and ethanol than higher-molecular-weight phthalates, finished articles are specified primarily for non-food-contact, short-service, or disposable applications. Published data for exact extraction values in specific PVC grades are limited, but comparative immersion tests show the trend consistently.

    Bulk handling of Kanatol 100 at production scale is conducted in closed storage tanks maintained at 25–35 °C with nitrogen blanketing or desiccant breathers to hold moisture below 0.10 % w/w. In-line refractive index monitoring at 27 °C provides early detection of cross-contamination with diethyl phthalate or dibutyl phthalate. Dimethyl phthalate is stable under recommended storage conditions, but hydrolysis can occur in the presence of strong acids, strong bases, or prolonged moisture ingress, liberating methanol and phthalic acid. Contact with strong oxidising agents should be avoided because ester oxidation can contribute to peroxide formation under extended air exposure.

    Regulatory records for DMP include EU REACH registration and evaluation under the applicable tonnage band for the manufacturer. DMP is not among the four phthalates restricted under RoHS Directive 2015/863 Annex II, but industrial hygiene controls remain necessary because of its vapour pressure and flammability. For food-contact uses, the formulator verifies that the specific compound or laminate meets the relevant indirect-additive regulation, such as 21 CFR 175.105 for adhesives or 21 CFR 176.170 for paper and paperboard components; DMP is not treated as a general direct-food-contact plasticizer. In aqueous and alcoholic extraction tests conducted per ISO 175, DMP migrates more readily than higher-molecular-weight phthalates, so applications involving prolonged contact with water, ethanol, or food simulants are avoided unless the finished structure demonstrates compliance through migration testing.