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Payal Polyplast Trioctyl Trimellitate (TOTM)

    • Product Name: Payal Polyplast Trioctyl Trimellitate (TOTM)
    • Factroy Site: Jiangjun Avenue 55#, Jiangning Area, Nanjing, China
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    • Manufacturer: Alchemist Worldwide Ltd
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    Specifications
    HS Code 443444
    Product Name Payal Polyplast Trioctyl Trimellitate (TOTM)
    Chemical Name Trioctyl Trimellitate
    Synonyms Tris(2-ethylhexyl) trimellitate; TOTM
    Cas Number 3319-31-1
    Ec Number 222-020-0
    Molecular Formula C33H54O6
    Molecular Weight 546.78 g/mol
    Appearance Clear, oily liquid
    Color Colorless to pale yellow
    Odor Mild ester-like odor
    Density 0.985 g/cm3 at 20°C
    Specific Gravity 0.982-0.988 at 25°C
    Viscosity 100-120 mPa·s at 20°C
    Refractive Index 1.485-1.490 at 20°C
    Boiling Point 414°C at 760 mmHg
    Flash Point >260°C
    Pour Point < -30°C
    Acid Value 0.10 mg KOH/g max
    Ester Content 99.0% min
    Purity 99.0% min
    Moisture 0.10% max
    Volatile Matter 0.20% max
    Saponification Value 300-310 mg KOH/g
    Solubility In Water Practically insoluble
    Solubility In Organic Solvents Soluble
    Thermal Stability Excellent
    Migration Resistance High
    Extraction Resistance Good
    Electrical Resistivity High

    As an accredited Payal Polyplast Trioctyl Trimellitate (TOTM) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of Payal Polyplast Trioctyl Trimellitate (TOTM)

    When TOTM Replaces DINP in 105°C Continuous-Service Automotive Wire Insulation

    Formulation development for thin-wall automotive primary wire begins with suspension PVC having a K-value of 70. TOTM is added at 50–70 phr after the resin reaches 70–80°C in a high-speed mixer, followed by Ca-Zn stabilizer at 5–7 phr, acid scavenger at 1–2 phr, and antioxidant at 0.3–0.8 phr. The batch is dropped at 125–135°C and cooled under agitation to 40°C before feeding a counter-rotating twin-screw extruder with L/D 36:1, compression ratio 2.5:1, and barrel zones of 150°C, 160°C, 170°C, and 175°C. At 50–70 phr TOTM, melt viscosity is higher than DINP at equal loading; breaker-plate pressure typically reaches 130–180 bar at a screw speed of 20–30 min⁻¹. The higher molecular weight of TOTM demands greater shear to produce a homogeneous melt, but barrel temperatures above 195°C initiate dehydrochlorination in unstabilised zones. Vent vacuum is therefore held below -0.08 MPa and die temperature is capped at 185°C.

    Thermal endurance is evaluated against ISO 6722-1 for class B and class C automotive cable. Insulation extruded to 0.35 mm wall thickness on a crosshead die at 150–200 m/min must retain at least 70% of original elongation after 3,000 h at 125°C when tested per ISO 188. TOTM-based compounds typically show Shore A hardness of 80–85 per ISO 868 and tensile strength of 18–22 MPa per ISO 37. Volume resistivity after 7 days at 85°C and 85% relative humidity remains above 1×10¹² Ω·cm per ASTM D257 when the stabilizer level is maintained at 5–7 phr. These values are production-compounding ranges and are not guaranteed batch data for every PVC lot. During wire extrusion, conductor preheat is set to 120–140°C to prevent die-entry freezing. The pressure drop through a 0.35 mm wall crosshead is higher with TOTM than with DINP; line speed on single-screw extruders with L/D 24:1 is reduced by 5–15% unless screw temperature is increased. The resulting insulation passes low-temperature winding at -40°C according to ISO 6722-1 without cracking when the compound is free of residual moisture.

    Compliance checklist for 105°C automotive wire insulation based on TOTM/PVC
    PropertyTest methodTypical evaluation condition
    Tensile strength and elongationISO 3723°C, 250 mm/min
    HardnessISO 86815 s dwell, Shore A
    Long-term thermal ageingISO 188125°C, 3,000 h
    Insulation resistanceASTM D257500 V DC, 23°C
    Low-temperature windingISO 6722-1-40°C, mandrel outer diameter

    Reprocessing of TOTM-based wire compound is limited to 10–20% in the virgin dry blend. Heat-exposed recyclate increases fusion time and reduces volume resistivity because partially degraded PVC absorbs plasticizer unevenly. On a Brabender Plastograph EC fitted with a W 50 E mixer, TOTM at 65 phr extends fusion-torque equilibrium by 20–40% compared with DINP at the same loading when tested at 175°C and 40 rpm. Strand pelletizer calibration must account for higher melt tack; die-face temperatures above 180°C cause sticking and discontinuous pellet geometry. Inkjet marking adhesion is generally improved on TOTM surfaces because trimellitate plasticizer does not bloom as readily as low-molecular-weight phthalates, but adhesion remains batch-dependent and requires corona pre-treatment above 38 dyn/cm.

    Why Is TOTM Specified for Blood-Contact PVC Tubing and Cytotoxicity-Screened Sets?

    Medical-grade PVC compound is prepared in a clean compounding area using suspension PVC with K-value 70–72 and residual vinyl chloride monomer below 1 ppm. TOTM is added at 40–55 phr with epoxidised soybean oil at 3–5 phr, Ca-Zn stabilizer at 1–3 phr, and processing aid at 0.1–0.3 phr. The dry blend is fed to a single-screw extruder with L/D 30:1 and a barrier screw, operating at 20–40 min⁻¹ with barrel zones of 155°C, 165°C, 170°C, and 175°C. Head pressure is maintained below 200 bar. The die is set at 180°C to produce 3.0 mm outer diameter tubing with 0.5 mm wall thickness. Solvent bonding of TOTM-based tubing shows no surface stress cracking after exposure to cyclohexanone for 5 minutes in standard production checks.

    Plasticizer migration is evaluated under ISO 10993-18. TOTM demonstrates lower extraction than DEHP in n-hexane and ethanol/water media because its higher molecular weight and branched alkyl chains restrict diffusion. Cytotoxicity is assessed per ISO 10993-5 using L929 mouse fibroblast cells, and irritation is assessed per ISO 10993-10. A chemical characterisation report must be generated for each stabilizer combination because leachable metal ions and organotin degradation products influence the overall biological evaluation. Mechanical properties after steam sterilisation at 121°C for 30 minutes remain within specification: elongation at break above 250% per ISO 37, Shore A hardness 65–75 per ISO 868. Gamma sterilisation at 25–40 kGy produces dose-dependent yellowing but does not introduce additional cytotoxic leachates from TOTM at levels that fail ISO 10993-5 in most formulations.

    Medical PVC compound compliance checklist
    EvaluationStandardCondition
    CytotoxicityISO 10993-5L929, 24 h extract exposure
    IrritationISO 10993-100.9% saline extract
    Chemical characterisationISO 10993-1850% ethanol/water, 37°C, 72 h
    SterilisationISO 11135EtO, 55°C, 60% RH

    Ethylene oxide sterilisation at 55°C with 600 mg/L EO and 60% relative humidity requires aeration at 50°C for at least 12 h. Residual EO in TOTM-based tubing is removed more slowly than in DEHP-based tubing due to lower gas permeability. This constraint applies to blood bags and dialysis sets that must meet ISO 3826. TOTM is not indicated for long-term implantable devices; the material remains plasticised PVC and retains a measurable leachable profile. Published data for specific TOTM-stabilizer combinations in implant-grade applications is limited.

    In automotive instrument panel skin production, calender or cast-film lines use TOTM to reduce interior fogging. A typical paste resin formulation contains 100 phr PVC with K-value 70, 65–75 phr TOTM, 3–5 phr epoxidised soybean oil, and 1–3 phr Ca-Zn stabilizer. The film is fused in a hot-air oven at 190–200°C for 3–5 minutes before embossing. Fogging is measured according to DIN 75201 method B or ISO 6452; TOTM-based formulations typically show reflectance values above 90% and gravimetric condensate below 1.0 mg. These results are batch-dependent and must be verified with the selected stabilizer package. Calender roll temperatures are held 5–10°C higher than DIDP-based material. Roll temperatures below 175°C produce visible unmelted resin particles and surface streaks; above 195°C, the compound yellows if thermal stabilizer is insufficient. Vacuum forming over a polyurethane foam substrate at 120–140°C requires sufficient low-temperature flexibility to avoid whitening at grain lines. The low fogging result establishes reduced volatile loss but is not interpreted as zero emission.

    Extraction Resistance in Fuel-Contact Hose and Static Seal Compounds

    For low-pressure fuel return lines and pump suction lines, PVC/NBR hose compounds are produced with TOTM at 40–60 phr, NBR at 15–25 phr, and PVC with K-value 70. Immersion testing per ASTM D471 in IRM 903 oil at 100°C for 70 h shows lower volume swell than DOP-based equivalents; the actual percentage is strongly influenced by NBR ratio and filler content. Compounds with Shore A 70–80 are extruded on a pin-type crosshead at 140–160°C. TOTM maintains plasticizer retention after fuel contact but is not suitable in high-aromatic gasoline service where nitrile rubber content above 40 phr is required for elastomeric sealing. Published data for this specific hose configuration is limited.

    Gelation Temperature, Solvency, and High-Shear Viscosity in TOTM Loaded Plastisols

    High-shear mixing of PVC paste resin with TOTM begins at 25°C liquid phase. TOTM has a Brookfield viscosity of approximately 250–350 mPa·s at 25°C using spindle #3 at 20 rpm. Paste resin with K-value 75 is charged into a dissolver at 1,500–2,000 rpm for 15–20 minutes and then vacuum-deaerated at -0.09 MPa for 30 minutes. At 60 phr TOTM, the plastisol has an initial Brookfield viscosity above 3,000 mPa·s; at 80 phr, viscosity falls to 1,500–2,500 mPa·s. Viscosity stability over 7 days at 23°C is better than branched phthalates, but room-temperature solvency is lower, requiring a co-solvent if extended pot life is specified.

    Fusion in a forced-air oven uses a two-stage profile: 140°C for 3 minutes to gel the film and 195°C for 5 minutes to form a dense continuous matrix. Dipped steel parts are preheated to 150°C. Insufficient gelation time at 140°C results in interlayer porosity and loss of adhesion per ASTM D413. The final coating has Shore A 75–85, tensile strength 12–16 MPa, and elongation 250–350% per ASTM D638. TOTM reduces tensile strength slightly relative to low-molecular-weight plasticizers at equal hardness because it increases free volume without increasing network density. Corrosion resistance of dipped coatings on phosphated steel is tested per ISO 9227; TOTM-based plastisols show no blistering for 500 h when edge coverage is complete.

    Outdoor exposure of single-ply PVC roofing membranes places simultaneous heat, UV, and mechanical stress on the plasticizer system. TOTM is used at 60–70 phr with PVC K-value 70–73 and liquid Ba-Zn or Ca-Zn stabilizer at 4–6 phr. The melt is processed on a calender at 165–185°C and drawn into 1.2 mm, 1.5 mm, or 2.0 mm sheet before embossing. Dimensional stability is tested according to EN 1107-2 at 100°C for 6 hours; the change in length must be below 0.5% for mechanically fastened systems. Cold flexibility is tested per EN 495-5 at -20°C; TOTM-based membranes show no cracking at -20°C, but published data for temperatures below -20°C is limited. Accelerated xenon-arc exposure per ISO 4892-2 at 0.35 W/m² and 340 nm with black-standard temperature 65°C and 18/102 min water spray shows retention of elongation above 80% after 5,000 h only if a UV screening package is present. Plasticizer volatility measured by activated carbon method per ISO 176 is below 1%, but this test is not a substitute for long-term service. Hot-air welding at 400–450°C produces seam strength of 80–90% of sheet tensile strength per EN 12317-2. TOTM is not suitable for membranes in contact with bitumen or coal tar products because aromatic oils extract trimellitate plasticizers.

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    Certification & Compliance
    More Introduction

    Payal Polyplast Trioctyl Trimellitate (TOTM) is a primary plasticizer based on the triester of trimellitic anhydride and 2-ethylhexanol. The active substance is tris(2-ethylhexyl) benzene-1,2,4-tricarboxylate, CAS 3319-31-1, with molecular formula C33H54O6 and molecular weight 546.78 g/mol. The product is supplied as a bulk liquid for compounding of flexible polyvinyl chloride, selected elastomeric systems, and high-temperature insulation compounds. Grade-specific model suffixes appear on the supplier certificate of analysis; published data for the exact Payal Polyplast grade are limited, so the following values are typical commercial TOTM ranges and should be verified against lot documentation.

    Commercial TOTM specifications normally require an ester content not less than 99.0%, an acid value not exceeding 0.1 mg KOH/g, water content not exceeding 0.10 wt%, and Pt-Co colour not greater than 50. Density at 20 °C falls within 0.985 g/cm³ to 0.991 g/cm³ when measured by ASTM D4052. Dynamic viscosity at 25 °C is typically 210 mPa·s to 260 mPa·s by ASTM D445. Refractive index at 25 °C is approximately 1.483 to 1.487 by ASTM D1218. These parameters influence metering accuracy, storage heating requirements, and the electrical cleanliness of the finished compound.

    Physical and Electrical Performance Boundaries of This Trimellitate Ester

    Liquid-state viscosity has direct processing consequences. At 25 °C, TOTM exhibits roughly 3.5 to 4.5 times the viscosity of DEHP. Production lines using volumetric dosing therefore maintain jacketed storage and transfer pipework at 35 °C to 45 °C to avoid pump cavitation and dose drift. In high-speed PVC dry blending, TOTM added below the dry-up temperature produces incomplete absorption, plate-out on mixer walls, and downstream screw slippage. Turbo mixers are typically discharged at 110 °C to 120 °C; the plasticizer should be added after the stabilizer has dispersed but before the blend reaches its final dry point. Batch-to-batch viscosity variation within the 210 mPa·s to 260 mPa·s range can require volumetric pump recalibration to prevent hardness drift in the finished compound.

    Electrical performance is closely linked to acid value and ionic purity. A maximum acid value of 0.1 mg KOH/g helps maintain high volume resistivity in PVC insulation. Plasticized compounds are evaluated under ASTM D257; the final resistivity depends on stabilizer type, filler, and moisture. The low residual acidity of TOTM supports insulation compounds intended for cable standards such as IEC 60227-1 and UL 1581, but the complete compound must pass the relevant end-product ageing and electrical test schedule.

    Thermal permanence is the principal reason for selecting TOTM over general-purpose phthalates. The high molecular weight and low vapour pressure reduce plasticizer loss during long-term thermal ageing. Comparative formulations at 70 phr plasticizer on PVC K 70 typically show lower weight loss for TOTM than for DEHP when tested by activated-carbon volatility methods such as ASTM D1203. The exact loss percentage depends on foil thickness, stabilizer package, and filler loading; supplier data should be consulted for the specific compound.

    How Does TOTM Function in High-Temperature PVC Insulation?

    The plasticizing mechanism is primarily physical. TOTM solvates amorphous PVC through polar interaction between ester carbonyl groups and carbon-chlorine dipoles of the polymer. The branched octyl groups increase free volume to a lesser extent than shorter linear plasticizers, which is why TOTM can require higher loading or higher processing temperature to reach a given hardness. Simultaneously, the molecular architecture raises the activation energy for diffusion through the polymer matrix, reducing vapour-phase mass loss and thereby improving retention of flexibility after thermal ageing.

    Wire and cable extrusion lines running TOTM-based compounds commonly use single-screw extruders with L/D 25:1 to 30:1 and compression ratio 3:1 to 3.5:1. Barrel temperatures are maintained between 150 °C and 185 °C to prevent premature PVC degradation while achieving fusion. Because TOTM raises melt viscosity relative to DEHP, die temperatures may need to be set 5 °C to 10 °C higher than for an equivalent DEHP compound, and head pressure should be monitored. Calendering lines processing TOTM-PVC typically set the first two roll nips at 165 °C to 185 °C and the final embossing roll at 150 °C to 170 °C. Small roll banks are preferred because the higher melt viscosity increases the risk of pitting and surface defects.

    For insulation rated for continuous conductor operation up to 105 °C, accelerated ageing is commonly performed at 136 °C for 168 h under UL 1581 or IEC 60811-401. TOTM-based compounds are formulated to retain tensile strength and elongation above the standard-specific minima. The plasticizer does not function alone; a thermally matched stabilizer system, typically mixed metal or lead-free calcium-zinc, is required to control dehydrochlorination during the test. In high-temperature PVC insulation, TOTM primarily addresses plasticizer loss, while the stabilizer controls polymer degradation.

    TOTM is not a direct drop-in replacement for DEHP in low-temperature flexibility applications. Plasticized PVC based on TOTM may exhibit a higher brittleness temperature than compounds based on dioctyl adipate or diisononyl adipate when measured by ASTM D746. Formulations targeting service temperatures below -30 °C should be evaluated with pilot-scale low-temperature testing because published data for this exact Payal Polyplast configuration are limited.

    Migration Resistance and Extraction Behaviour in Automotive and Medical Matrices

    In automotive interior films, instrument panel coverings, and steering-wheel skins, fogging is measured by ISO 6452 or DIN 75201. TOTM is selected because its low vapour pressure reduces condensable emissions compared with DEHP or DINP. The benefit is less pronounced under aggressive fluid extraction. In flexible PVC sheeting tested by ASTM D1239, TOTM typically shows lower aqueous-soap extraction than DEHP, but the difference narrows in hexane or synthetic lipid simulants. The improvement is therefore application-specific rather than universal.

    For medical and pharmaceutical tubing, TOTM can only be considered after the compound manufacturer qualifies the raw material under ISO 10993-1 and leachables testing under ISO 10993-18. TOTM is a monomeric plasticizer, not a polymeric plasticizer. In lipid-rich media its migration rate exceeds that of high-molecular-weight polyadipate or polyester plasticizers. Any extraction-resistance claim must be based on the final sterilized device and its intended contact medium, not on the plasticizer alone.

    Diffusion-controlled migration in PVC follows a Fickian mass-transfer model. The higher molecular volume of TOTM lowers the diffusion coefficient relative to DEHP at ambient temperature, but the difference decreases as temperature rises. Accelerated extraction tests at elevated temperature may therefore underestimate long-term performance benefits at service temperature. This behaviour is relevant when comparing TOTM with lower-viscosity non-phthalate alternatives such as DOTP.

    When Phthalate-Free Specifications Force a DOTP-to-TOTM Transition

    When a phthalate-free specification is issued, DOTP is often the first substitution because of its lower viscosity and similar molecular weight to DEHP. The transition to TOTM becomes justified when the application is exposed to sustained heat above 90 °C or when long-term low volatility is critical. TOTM has a molecular weight of 546.78 g/mol, whereas DOTP has 390.56 g/mol. The molecular weight difference reduces plasticizer loss but increases viscosity and processing difficulty.

    The following table compares typical liquid properties of TOTM with general-purpose phthalate and non-phthalate plasticizers. The values are drawn from publicly available commercial product ranges and are not a substitute for the Payal Polyplast certificate of analysis.

    PlasticizerCAS registry numberMolecular weightTypical viscosity at 25 °CDensity at 20 °CMain processing trade-off
    TOTM3319-31-1546.78 g/mol210–260 mPa·s0.985–0.991 g/cm³High permanence, higher melt viscosity
    DOTP6422-86-2390.56 g/mol60–70 mPa·s0.980–0.990 g/cm³Lower viscosity, lower permanence
    DEHP/DOP117-81-7390.56 g/mol55–60 mPa·s0.984–0.986 g/cm³General-purpose phthalate, higher volatility
    DINP68515-48-0418.61 g/mol85–115 mPa·s0.970–0.980 g/cm³Phthalate status, moderate permanence

    A production line switching from DOTP to TOTM may require several operational changes. Storage and dosing temperatures should be raised to 35 °C to 45 °C. Dry-blend absorption is slower; high-speed mixers may need to remain at 110 °C to 120 °C until the torque rise stabilizes. Extruder screw speed may need reduction if melt pressure rises excessively. Gravimetric dosing is preferred over volumetric dosing because TOTM viscosity varies more with temperature within the normal plant window.

    Regulatory status is application-specific. TOTM is not one of the four phthalates restricted under EU RoHS Directive 2011/65/EU. REACH registration under EC 1907/2006 should be confirmed on the supplier safety data sheet. Medical or food-contact suitability must be demonstrated on the final article under the relevant regulation; raw-material supply does not by itself confer end-product clearance.

    Standard or regulationScopeRelevance to TOTM
    EU REACH EC 1907/2006Registration, evaluation, authorisation of chemical substancesRegistration status must be verified on the safety data sheet
    EU RoHS 2011/65/EURestricted phthalates in electrical and electronic equipmentCAS 3319-31-1 is not DEHP, BBP, DBP, or DIBP
    EU Toy Safety Directive 2009/48/ECChemical migration limits in toysTOTM must be evaluated in the final toy material if applicable
    ISO 10993-1Biological evaluation of medical devicesFinal-device qualification is required; raw-material data are not sufficient

    Operational boundaries include storage above 15 °C to avoid excessive viscosity increase and below 50 °C to limit oxidative colour drift. Stainless steel 316L or lined mild steel is preferred for storage vessels when low colour retention is specified. Prolonged contact with strong aqueous alkalis should be avoided because ester hydrolysis increases acid value and may reduce electrical resistivity. When relative humidity exceeds 60%, dry-air or nitrogen blanketing is recommended to prevent moisture pickup in bulk storage.