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| HS Code | 438096 |
| Productname | Bluesail Trioctyl Trimellitate (TOTM) |
| Chemicalname | Tris(2-ethylhexyl) trimellitate |
| Casnumber | 3319-31-1 |
| Einecsnumber | 222-020-0 |
| Molecularformula | C33H54O6 |
| Molecularweight | 546.79 g/mol |
| Appearance | Colorless to pale yellow transparent oily liquid |
| Purity | ≥99.5% |
| Colorapha | ≤50 |
| Densityat20c | 0.985-0.995 g/cm³ |
| Refractiveindexat20c | 1.483-1.487 |
| Viscosityat20c | 250-350 mPa·s |
| Flashpoint | ≥260 °C |
| Boilingpoint | >400 °C |
| Acidvalue | ≤0.05 mg KOH/g |
| Moisturecontent | ≤0.1% |
| Volatilematter | ≤0.1% |
As an accredited Bluesail 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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Extrusion-grade PVC compounds formulated for continuous conductor operating temperatures of 105 °C and 125 °C routinely employ trioctyl trimellitate (TOTM; CAS 3319-31-1; molar mass 546.8 g·mol⁻¹) at loadings of 45–60 phr per 100 phr PVC resin. The plasticizer is introduced in a hot dry-blend stage at 120–130 °C for 8–12 min in a high-speed mixer, followed by cooling to 40–45 °C before compounding. On a 65 mm counter-rotating twin-screw extruder with L/D 25:1 and vacuum venting, barrel zones are typically set at 160/165/170/175/180 °C, with melt temperature held between 168 °C and 184 °C; lower barrel temperatures produce unmelted resin particles that appear as surface pips in the extruded insulation, while higher settings accelerate dehydrochlorination and shift colour toward amber. The compound is pelletized under water-ring cooling and dried at 80 °C for 2 h when ambient relative humidity exceeds 60%, because residual moisture in calcium-zinc or organotin stabilizer packs causes surface porosity during jacket extrusion. Final insulation properties are assessed by ASTM D638 for tensile strength and elongation retention after 7 days at 121 °C, ASTM D257 for volume resistivity, and UL 1581 for unaged and aged performance; typical values for a 50 phr TOTM compound fall near 18–21 MPa tensile strength, 280–340% elongation at break, and volume resistivity above 1×1012 Ω·cm, although exact values shift with resin K-value and filler type. Processing conflicts arise when line speed exceeds 250 m/min on thin-wall automotive primary wire, because melt fracture initiates at the die land if the TOTM-containing compound has not been pre-conditioned with 0.3–0.6 phr external lubricant; field records from cable extrusion lines correlate die-lip build-up with excessive zinc stearate, which reacts with the trimellitate ester at elevated head pressure. The formulation boundary is usually 70 phr: above this loading, hardness drops below Shore A 82 and the insulation may fail crush-resistance requirements specified in UL 1581 for building wire constructions. Halogenated flame-retardant packages containing antimony trioxide at 3–5 phr remain compatible, but amine-terminated processing aids should be excluded because amine attack on the ester can reduce thermal life under 136 °C heat-shock testing.
| Standard designation | Measured property | Typical acceptance window |
|---|---|---|
| UL 1581 | Unaged tensile strength | ≥ 10.3 MPa |
| UL 1581 | Unaged elongation at break | ≥ 100% |
| UL 1581 | Tensile retention after 7 days at 121 °C | ≥ 65% |
| UL 1581 | Elongation retention after 7 days at 121 °C | ≥ 65% |
| ASTM D257 | Volume resistivity at 20 °C | ≥ 1×1012 Ω·cm |
| IEC 60227 | Insulation resistance at 70 °C | ≥ 0.005 MΩ·km |
In slush-moulded and vacuum-formed automotive interior skin production, TOTM is introduced at 50–70 phr where DIN 75201 fogging and ISO 6452 condensate values cannot be met by lower-molecular-weight phthalates; the trimellitate structure reduces plasticizer volatilization at 100 °C because of molar mass 546.8 g·mol⁻¹, slower diffusion through the amorphous PVC matrix, and lower vapour pressure. In dry-blend slush powder operations, TOTM-containing dry-blends are sieved to 250–400 μm before being rotated in a heated tool at 220–240 °C for 60–120 s, producing skins with thickness between 0.8 mm and 1.4 mm. Field observations on slush-moulding lines show that TOTM can increase powder clumping when mixer outlet temperature exceeds 45 °C; a cooled post-mixing step is therefore used before bagging. The resulting skins exhibit lower surface tack after accelerated thermal ageing at 100 °C for 24 h, measured by weight change during activated-carbon volatility testing per ASTM D1203, with TOTM-containing films generally showing losses below 1.0% under conditions where dioctyl phthalate can exceed 3.0%. Vacuum-formed instrument panel covers with TOTM require sheet preheat temperatures between 165 °C and 185 °C; below 155 °C, the sheet splits along grain lines, and above 190 °C, gloss variation appears on the formed surface. Compliance testing for interior air quality uses VDA 278 thermal desorption, where total VOC and fogging residues must be reported; TOTM is generally classified as a low-emission plasticizer suitable for compounds targeting total VOC below 250 μg/g, but compound-specific published data for complete skin laminates is limited. The main incompatibility is with certain acrylic surface coatings that contain strong acid catalysts, which can hydrolyze the ester if curing temperatures exceed 120 °C; adhesion testing per ISO 2409 should be repeated for each coating batch.
In short-term extracorporeal fluid circuits and medical tubing, TOTM is selected at loadings below 40 phr primarily to reduce plasticizer migration into aqueous media under intermittent flow, not to maximize flexibility. The compound must pass ISO 10993-5 cytotoxicity, USP 87 biological reactivity, and extraction tests such as ISO 10993-12 with ethanol/water or phosphate-buffered saline; the high molecular weight and low water solubility of TOTM support lower extraction values than conventional phthalates in the same PVC matrix. Peristaltic pump tubing compounds typically add 5–15 phr of epoxidized soybean oil as co-stabilizer and incorporate a calcium-zinc stabilizer package; the dry-blend is pelletized before single-screw tubing extrusion, with melt temperature controlled below 175 °C to avoid yellowing. In production, tubing lines running 10–25 m/min observe die-lip exudation when TOTM loading approaches 55 phr and barrel temperature exceeds 180 °C; the exudate is not free plasticizer but a stabilizer-plasticizer interaction film removable by periodic wiping. Published long-term spallation data for TOTM-containing PVC in roller-pump circuits with occlusion cycles exceeding 106 is limited; manufacturers therefore validate pump life empirically on each tubing lot. Steam autoclaving at 121 °C for 30 min can induce surface haze if the epoxy stabilizer concentration is below 5 phr; the haze does not necessarily indicate plasticizer extraction but alters surface topology sufficiently to affect ultrasonic welding and solvent bonding of connectors. The use of TOTM in implantable-grade PVC is not established by the same volume of public extractables data as DEHP; risk assessments under ISO 10993-1 should therefore be compound-specific.
A plastisol line running continuous knife-over-roll coating on woven polyester scrim uses TOTM at 55–65 phr when the finished belt cover must survive sustained service at 70 °C without edge cracking. The plastisol is prepared in a high-shear dissolver, de-aerated under vacuum at 50–100 mbar for 15–30 min, and applied at 300–500 g/m² dry coat weight. Gelation in a multi-zone oven proceeds from 170 °C to 210 °C over 60–90 s; under-fusion at the substrate interface appears as delamination during a 180° flex test and reduces peel adhesion measured per ISO 2411 below 3 N/mm. TOTM maintains cover flexibility after 7 days at 100 °C, shown by elongation retention per ISO 1421; the trimellitate also lowers volatile loss during oven residence, which reduces condensate accumulation on exhaust ductwork and decreases fire risk in continuous ovens. The processing boundary for knife-over-roll is plastisol viscosity: at TOTM loadings above 70 phr and shear rate 10 s⁻¹, viscosity may fall below 1500 mPa·s, causing strike-through on open-weave fabrics; below 45 phr, the plastisol may exceed 3500 mPa·s and generate uneven coating thickness. Published data on abrasion loss of TOTM-containing PVC belting covers under ISO 4649 remains formulation-dependent; filler type and particle size dominate wear behaviour more than plasticizer choice.
In photovoltaic-grade PVC compounds, the substitution of TOTM proceeds from the need to pass long-term thermal endurance at 120 °C under EN 50618 and IEC 62930 without adding a polyamide outer layer. Compounds based on 45–55 phr TOTM, a calcium-zinc stabilizer, and 3–5 phr of an acid scavenger are dry-blended and twin-screw pelletized; the melt temperature is held between 170 °C and 185 °C to limit thermal history before the cable extrusion step. The sheathing line typically uses a 90 mm single-screw extruder with L/D 25:1 and a crosshead die, with head pressure between 150 bar and 250 bar; screen packs finer than 80 μm are avoided because they raise melt temperature locally and accelerate dehydrochlorination. Low-temperature impact after -40 °C exposure is assessed by IEC 60811-504, and weathering resistance is screened under ASTM G154 for 720 h; formulations with TOTM generally retain elongation above 70% after UV/condensation cycling if carbon black dispersion is optimized to ≤2 μm agglomerate size. The critical process conflict is between high TOTM loading, which improves heat ageing, and surface roughness of the cable jacket: above 60 phr, the compound may exhibit die-lip exudation at line speeds below 15 m/min, producing an irregular surface that can trap dirt during outdoor exposure. Volume resistivity after 7 days in 80 °C water is measured at 500 V DC in qualification programs aligned with EN 50618, with water uptake and ionic contamination controlled by filler selection. Halogen content and flame retardancy for photovoltaic cables is governed by EN 50399 and IEC 60332-1-2; TOTM does not materially alter the oxygen demand of the PVC compound, but compound density and plasticizer volatility must be monitored to maintain consistent flame-test performance.
Where appliance wiring and moulded grommets require 105 °C service with reduced plasticizer exudation into ABS or polycarbonate enclosures, TOTM is incorporated at 35–50 phr in flexible PVC injection-moulding compounds. The compound is first pelletized to ensure uniform plasticizer distribution; then injection moulding proceeds at melt temperatures of 180–195 °C with mould temperature between 30 °C and 50 °C. Dimensional stability and Shore A hardness between 75 and 85 are achieved by varying filler level, while tensile strength per ASTM D638 usually falls between 14 MPa and 18 MPa. The key failure mode on production lines is stress-cracking of polycarbonate connectors caused by plasticizer migration; TOTM-containing PVC reduces this risk relative to low-molecular-weight phthalates because the larger molecule diffuses more slowly, but direct contact with uncoated polycarbonate should still be validated by thermal cycling at 85 °C and 85% RH for 500 h. Injection screw recovery time can increase by 15–25% compared with DOP-based compounds because the higher-viscosity TOTM plasticizer raises melt viscosity at equivalent hardness; barrel temperature profiling and screw back pressure below 10 bar are used to prevent overheating. No single test captures the full migration behaviour; manufacturers combine ASTM D1203 activated-carbon volatility, ASTM D3291 exudation testing, and end-use contact stress tests.
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Bluesail Trioctyl Trimellitate (TOTM) is supplied as a single-grade monomeric ester identified by CAS 3319-31-1 and EINECS 222-020-0, with molecular formula C33H54O6 and molecular mass 546.8 g/mol. The product is a branched triester formed from trimellitic anhydride and 2-ethylhexyl alcohol; the branching contributes to a higher flash point and lower vapour pressure than linear C8 phthalate or terephthalate plasticizers of equivalent carbon number. In manufacturer certificates of analysis, the ester content is controlled at ≥99.0% by gas chromatography, acid value ≤0.07 mg KOH/g, moisture ≤0.10%, and Pt-Co color ≤40. Density at 20°C is typically 0.984–0.990 g/cm³ under ASTM D4052, and dynamic viscosity at 25°C is typically 200–300 mPa·s under ASTM D445. The TOTM designation itself differentiates the ester from the company’s phthalate and terephthalate plasticizer lines; no additional numeric grade suffix appears in current Bluesail commercial documentation. Its primary application is in flexible PVC where prolonged thermal aging, low volatility, and resistance to extraction by soap or hydrocarbon are required. The main operational limitation is the slower absorption into PVC dry blends caused by the 546.8 g/mol molecular mass and branched structure, which becomes measurable as higher mixer torque or longer dry-up time.
In comparative plasticizer selection, the trimellitate ester differs from DEHP and DINP in molecular architecture and response to heat. The molecular mass of 546.8 g/mol is higher than 390.6 g/mol for DEHP and 418.6 g/mol for DINP; this directly reduces plasticizer volatility in elevated-temperature service. In supplier technical literature, air-oven volatility loss tested according to ASTM D1203 for 24 h at 100°C is commonly reported below 1% for TOTM-containing PVC, whereas DEHP-plasticized compounds often exceed 4% under the same protocol. Extraction resistance follows a similar pattern because the branched trimellitate migrates into non-polar fluids more slowly than the lower molecular mass ortho-phthalates. The trade-off appears in low-temperature flexibility, where TOTM compounds typically show a stiffer response than linear phthalate or sebacate alternatives. Cold-flex data generated by ASTM D1043 or torsion modulus methods are formulation-dependent; published data for this specific configuration are limited, and compounders should verify the brittle point against the lowest service temperature required by ISO 6722 or UL 1581.
The following ranges are representative comparative values for flexible PVC compounds at 67 phr plasticizer in a K 70 PVC resin; they are reproduced from supplier technical bulletins and are not product specifications.
| Property | DEHP | DINP | Bluesail TOTM |
|---|---|---|---|
| Molecular mass g/mol | 390.6 | 418.6 | 546.8 |
| Air-oven volatility loss 24 h/100°C, % ASTM D1203 | 4.0–5.0 | 1.5–2.5 | 0.3–0.8 |
| Tensile strength MPa ASTM D638 | 18–20 | 19–21 | 20–22 |
| Elongation at break % ASTM D638 | 320–360 | 310–350 | 290–330 |
| Low-temperature flex point °C ASTM D1043 | -28 to -32 | -26 to -30 | -18 to -22 |
In multi-layer automotive interior laminates, separation of TOTM from PVC depends on the concentration gradient at the interfacial layer and the sink properties of the adjacent polyurethane or polyolefin foam. Because TOTM has a lower diffusion coefficient than DEHP in flexible PVC at the same temperature, migration into polyurethane foam is slower; however, steady-state mass transfer is also controlled by solubility parameter and available sink thickness. On production lines, the observed failure mode is not bulk exudation but edge staining after 7–14 days at 70°C stack aging. The stain mass is often below gravimetric detection but visible on light-colored surfaces. To manage this, processors reduce TOTM addition to 50–60 phr or introduce a barrier layer. Published data for this specific configuration is limited, so accelerated stack aging and surface reflectance measurements are used for lot acceptance.
TOTM and dioctyl terephthalate both serve as non-ortho-phthalate alternatives, but TOTM is a triester with three 2-ethylhexyl groups on an aromatic 1,2,4-tricarboxylate core, whereas DOTP is a diester of terephthalic acid with two 2-ethylhexyl groups. That structural difference increases molecular mass by approximately 156 g/mol and raises carbonyl density for PVC solvation. The practical result is that TOTM offers lower volatility and higher heat-aging retention, while DOTP absorbs faster in dry blends and produces lower compound viscosity. Selection between the two in wire and cable compounds depends on whether the process is limited by line speed or by thermal aging. In high-output dry-blend systems where mixer cycle time is fixed below 300 s, DOTP may be preferred; in 105°C-rated insulation, TOTM often replaces DOTP despite the slower absorption.
Processing evaluations at 60–100 phr addition on counter-rotating twin-screw extruders with L/D 40:1 show that TOTM produces a measurable delay in torque stabilization during the first 4–6 L/D of the feed zone. In production-scale lines, the high-speed mixer discharge is held at 120–130°C to allow the ester to absorb before extrusion. Screw oil temperatures of 160–175°C and die head set points of 180–195°C are used for 105°C-rated insulation compounds; actual melt temperature is commonly 8–12°C above the die set point because of viscous shear heating. When the incoming PVC resin K-value shifts by ±2, the final melt temperature can drift by 5–8°C, requiring a screw speed adjustment of 10–15 min⁻¹ to hold dimensional stability. Vacuum venting below -0.08 MPa gauge is maintained to remove residual 2-ethylhexanol and moisture without causing melt pool instability. If TOTM is stored at relative humidity above 60%, the moisture content can exceed the 0.10% certificate limit after repeated partial container discharges; nitrogen blanketing or pre-drying is recommended. Plate-out in the calibration sleeve is reduced when free acidity is kept below 0.07 mg KOH/g, because residual trimellitic acid can react with metal stearate stabilizers and form deposits at the die exit.
Batch-to-batch control for Bluesail TOTM is centered on acid value and moisture rather than on color alone, because residual trimellitic acid and water influence downstream PVC heat stability more directly than Pt-Co color. In statistical process control monitoring of incoming tankers, the ester content and acid value are tracked on every lot; a shift in acid value from 0.04 mg KOH/g to 0.07 mg KOH/g can reduce the thermal stability time of a barium-zinc-stabilized compound by several minutes at 180°C in an oven test. This effect is handled by adjusting the stabilizer level, but only after verification by compound heat stability according to ISO 182-3. Moisture ingress during storage is a more common batch-to-batch failure than impurity drift, particularly when the product is stored in partially filled tanks under fluctuating humidity. Published data for this specific supplier’s tank storage variability is limited, so users should conduct moisture verification at receipt rather than relying solely on the certificate value.
Compliance with UL 1581 and ISO 6722 requires that the plasticizer not only reduces PVC melt viscosity but also resists surface loss at elevated continuous-use temperatures. TOTM is evaluated by compounding with a mixed metal stabilizer and antioxidant package, then extruding into conductor cross-sections of 0.5–1.5 mm². After air-oven aging at 136°C for 168 h, retained elongation values above 70% of original are commonly targeted; the branched trimellitate’s low volatility supports this better than DEHP or DINP. The same branching that suppresses volatility also reduces plasticizer migration to copper surfaces, which is relevant for tinned-copper conductor adhesion. In extraction testing using ASTM D1239 soap solution or ASTM D543 hydrocarbon exposure, TOTM-containing compounds show lower mass change than equivalent DEHP compounds. These effects are widely documented in comparative wire and cable formulations, though compound-specific retention should be measured by the cable manufacturer because stabilizer type and filler content can shift aging results by ±15%.
In wire and cable compounds, the plasticizer must not compromise volume resistivity. TOTM-plasticized PVC generally exhibits volume resistivity in the range of 1012–1013 Ω·m when measured under ASTM D257 after conditioning at 20°C and 50% relative humidity. This is comparable to other monomeric plasticizers, but the lower volatility of TOTM helps retain surface resistivity after thermal aging. The main electrical concern is residual ionic contamination from incomplete esterification; the acid value specification of ≤0.07 mg KOH/g and the low moisture limit reduce conductive ionic species. Compound volume resistivity should nevertheless be measured on the final formulation, because stabilizer and filler contributions can alter the result by more than one order of magnitude.
Regulatory documentation for Bluesail TOTM should be verified against the current safety data sheet and certificate of analysis, because registration status differs by region and end-use. The supplier compliance checklist typically includes the following standards for industrial plasticizer applications.
| Regulatory framework | Standard or clause | Typical verification |
|---|---|---|
| EU REACH registration | EC 1907/2006 | Registration number and tonnage band on SDS |
| EU RoHS Recast | Directive 2011/65/EU | Not an intentionally added restricted phthalate |
| Food contact | Commission Regulation (EU) 10/2011 | Article-specific migration testing required |
| PVC cable standard | UL 1581 | Compound formulation test |
| Plasticizer acid value | ASTM D1045 or equivalent | ≤0.07 mg KOH/g |
The ester is incompatible with strong oxidizing agents and with reactive metal surfaces above recommended processing temperatures. In PVC formulations, free amine-based antistatic additives at alkalinity above 0.05% can produce color drift after heat aging. Partial substitution of TOTM with faster-absorbing plasticizers may be required in high-output dry-blend systems where mixer cycle time is fixed below 300 s. In such cases, the TOTM fraction is typically limited to 40–50 wt% of the total plasticizer package unless the mixer discharge temperature can be increased to 130°C.