+8615371019725
| HS Code | 338855 |
| Brand | Bluesail |
| Productname | Bluesail Dioctyl Sebacate (DOS) |
| Chemicalname | Bis(2-ethylhexyl) sebacate |
| Casnumber | 122-62-3 |
| Einecsnumber | 204-558-8 |
| Molecularformula | C26H50O4 |
| Molecularweight | 426.67 g/mol |
| Appearance | Colorless to pale yellow transparent oily liquid |
| Purity | ≥99.5% |
| Density | 0.912-0.916 g/cm³ at 20°C |
| Meltingpoint | -55°C |
| Boilingpoint | 377°C |
| Flashpoint | ≥210°C |
| Refractiveindex | 1.450-1.455 at 20°C |
| Viscosity | 20-25 mPa·s at 20°C |
| Acidvalue | ≤0.1 mg KOH/g |
| Moisture | ≤0.1% |
| Colorapha | ≤50 |
| Estercontent | ≥99.5% |
| Volatilematter | ≤0.1% |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited Bluesail Dioctyl Sebacate (DOS) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Arctic-grade PVC insulation compounds for heavy-duty mobile cable are prepared from suspension PVC with a K-value of 70–72 and Bluesail dioctyl sebacate (DOS) as the primary low-temperature plasticizer at 35–45 phr. The ester is specified before compounding with an ester content not less than 99.0%, an acid number not more than 0.05 mg KOH/g, and a moisture content not more than 0.05%. A representative dry blend contains 4–7 phr calcium-zinc stabilizer, 3–5 phr epoxidized soybean oil co-stabilizer, 0.2–0.5 phr hindered phenolic antioxidant, and 0.3 phr stearic acid external lubricant. Mixing is performed in a high-intensity turbo-mixer heated to 110–120 °C, followed by discharge to a cooling mixer at 40 °C. The cooled dry blend is compounded on a corotating twin-screw extruder with L/D ratio of 30:1–40:1, with barrel temperatures from 140 °C in the feed zone to 175 °C at the die. Vacuum venting at -0.08 MPa removes residual moisture and volatile fractions before strand pelletizing. Laboratory fusion control uses a torque rheometer under ASTM D2538, with bowl temperature set at 160 °C and rotor speed at 30 rpm, to compare gelation time against phthalate-based reference compounds.
The lower solvating capacity of DOS compared with faster-gelling phthalates requires a longer dry-up period in the extruder. Below 110 °C, the blend remains grainy and produces a rough melt with visible unplasticized resin domains. Above 175 °C, die swell increases and plasticizer fuming becomes measurable on production-scale lines, requiring local exhaust ventilation and reduced screw speed. The practical processing window is therefore narrow, and batch-to-batch variation in PVC resin particle size distribution can shift the onset of fusion by 3–5 °C. Melt temperature at the die and extruder current draw are monitored continuously to detect abnormal plasticization. Above 45 phr, compatibility testing under ASTM D3291-22 becomes the limiting requirement rather than low-temperature flexibility, because constrained geometry and thermal aging can promote exudation. Tensile properties are measured on ASTM D638 Type IV specimens, low-temperature winding is evaluated under ISO 6722 at -40 °C, and finished cable jackets are checked under UL 1581 cold bend methods. Terminal applications include offshore wind inter-array cable sheathing, Arctic mining cable, and EV charging cable insulation where non-phthalate declarations are required.
| Standard/Regulation | Clause or Method | Checkpoint for DOS-Containing PVC Insulation |
|---|---|---|
| EU RoHS 2011/65/EU | Annex II restricted substances | DOS is not a restricted phthalate; verify phthalate-free stabilizer and pigment package |
| REACH SVHC Candidate List | Current published list | Supplier declaration of DOS non-SVHC status and intended use |
| EN 50620 | EV charging cable requirements | Low-temperature flexibility and non-phthalate plasticizer validation |
| UL 1581 | Cold bend test method | No jacket cracking at specified mandrel diameter and conditioning temperature |
| ASTM D3291-22 | Plasticizer compatibility under compression | No exudation after heat aging at 100 °C for 168 h |
Plastisol-coated polyester fabrics for cold-storage curtains and truck side curtains are produced from PVC paste resin with a K-value of 72, Bluesail DOS at 65–85 phr, 5 phr epoxidized soybean oil, 3 phr calcium-zinc stabilizer, and 5–10 phr aliphatic hydrocarbon viscosity reducer. The liquid formulation is dispersed in a Cowles high-shear dissolver at impeller tip speeds of 6–10 m/s for 15–20 min, then vacuum-deaerated at -0.095 MPa until Brookfield RVT viscosity measured with spindle #6 at 20 rpm stabilizes between 2,200 mPa·s and 3,200 mPa·s. Viscosity retention after 24 h is recorded because DOS-based plastisols can show slight shear-rate-dependent recovery that affects knife-over-roll coating weight control.
Knife-over-roll coating applies a wet film of 200–400 µm to polyester scrim, followed by oven gelation at 160–180 °C for 2–3 min. Because DOS solvates PVC emulsion resin more slowly than DINP, line speed must be reduced or oven length increased to achieve full film fusion. Incomplete gelation appears as mud cracking on flexure and poor scrub resistance, while excessive oven temperature volatilizes the low-viscosity diluent and can leave surface pinholes. After conditioning, coated fabric tensile properties are measured under ISO 1421, and low-temperature bend resistance is checked under ISO 4675 at -30 °C. The finished material is fabricated into roll-up cold-room doors, refrigerated truck side curtains, and lifeboat cover panels where repeated flexing at sub-zero temperatures is required.
In environmentally acceptable hydraulic fluid compounding, Bluesail DOS functions as a low-temperature co-basestock in HEES-type synthetic ester fluids rather than as a conventional plasticizer. A typical blend contains 20–45 wt% DOS, 50–75 wt% high-oleic vegetable oil or trimethylolpropane trioleate, 1.0–1.5 wt% ashless antiwear additive, 0.5–1.0 wt% phenolic antioxidant, and 0.2–0.4 wt% rust inhibitor. Components are charged to a heated blending vessel at 45–60 °C, stirred under nitrogen, and filtered through 5 µm absolute media before drumming. DOS contributes to a kinematic viscosity that places the neat ester close to ISO VG 10–15 at 40 °C, with viscosity index approaching 150 and pour point below -50 °C. Finished ISO VG 32 and 46 fluids therefore retain low-temperature pumpability without heavy naphthenic diluents. Conformance is verified under ISO 3104 for viscosity, ISO 2592 for flash point, and ISO 15380 for HEES subcategory requirements. Hydrolytic stability is the principal operational boundary: continuous exposure to free water above 0.1 wt% increases acid number, and service-fluid condition monitoring under ASTM D974 is used with an alarm limit of 0.5 mg KOH/g. Published data for this specific Bluesail DOS blending configuration is limited, so each finished lubricant formulation is validated through pumpability and hydrolysis testing rather than by extrapolation from neat ester data.
Nitrile rubber compounds for cold-service seals in oilfield valves and pneumatic actuators are mixed in two-stage cycles. A first-stage masterbatch consists of low-ACN NBR with 28–34% acrylonitrile content, 10–20 phr Bluesail DOS, 40–60 phr N550 carbon black, 5 phr zinc oxide, and 1 phr stearic acid. Production mixing uses a 45 L or 75 L internal mixer at fill factor 0.75, with discharge temperature controlled below 130 °C to prevent premature sulfur crosslinking. The second stage adds 1.5 phr sulfur and 1.5 phr TBBS accelerator on an open mill at 60–70 °C. The use of DOS in the masterbatch reduces mechanical shear heating and improves carbon black dispersion compared with aromatic ester plasticizers, but it also prolongs cure induction time during subsequent molding.
DOS at 10–20 phr reduces the ASTM D2137 Method A brittleness temperature into the -40 °C to -45 °C range for low-ACN grades, but the same addition increases volume swell recorded under ASTM D471 after 70 h in IRM 903 oil at 100 °C. Above 15 phr, tensile strength decreases and compression set after ASTM D395 Method B for 22 h at 100 °C tends to rise, constraining the formulation space. A production bottleneck appears in injection molding: higher DOS loadings delay cure and increase mold fouling at typical cure temperatures of 170–180 °C. Compounds are therefore validated by moving-die rheometer torque, compression set, and oil-resistance testing before release to full-scale seal production. Terminal parts include O-rings, flange gaskets, and valve stem seals for Arctic and subsea service where phthalate-free sealing elements are specified.
PVC conveyor belting for food-processing environments uses DOS as a phthalate-free primary plasticizer at loadings from 30 phr to 50 phr in a suspension PVC matrix with K-value 70. The stabilizer package combines calcium-zinc carboxylates at 4–6 phr with epoxidized soybean oil at 3–5 phr. The dry blend is processed through a counterrotating twin-screw extruder at melt temperatures below 185 °C, then calendered or laminated onto polyester fabric plies. DOS is listed in FDA 21 CFR 178.3740 for use as a plasticizer in polymeric substances intended for food-contact articles, but the finished conveyor belt must meet end-use extraction limits under the applicable food-simulant protocols specified by the belt manufacturer and regulatory reviewer. Volatility is characterized by ASTM D1203; extractable content in hexane or other specified food simulants is tested on finished belt specimens before approval.
A critical limitation is oil and solvent extraction: compared with high-molecular-weight polymeric plasticizers, monomeric sebacate esters can migrate more readily into fatty food simulants, so barrier layers or lower DOS loadings may be required for direct high-fat contact. Published migration data for this specific Bluesail DOS conveyor belt configuration is limited; each belt construction is therefore validated empirically under the intended food-simulant exposure schedule rather than by extrapolation from neat resin data. The production line also requires frequent die-lip cleaning because residual acid values above 0.05 mg KOH/g can promote stabilizer plate-out. Finished belt applications include phthalate-free conveying systems for bakery, meat, and frozen food processing where low-temperature flexibility and regulatory documentation are jointly specified.
Flexible PVC profiles for refrigerator door gaskets and cold-room seals are coextruded with a soft skin based on PVC K-value 65–68, Bluesail DOS at 50–70 phr, 3–5 phr calcium-zinc stabilizer, and 3 phr epoxidized soybean oil. The rigid profile substrate is produced in the same line using high-K PVC without plasticizer; both melt streams are combined in a coextrusion die at 170–185 °C. DOS provides a lower brittle point than dioctyl adipate after long-term aging while retaining sufficient permanence for gasket flexing at -35 °C to -40 °C. ASTM D746 brittleness testing and ASTM D3291 exudation testing are used as incoming and finished-part quality gates. The principal process boundary is die lip plate-out: sebacate esters with residual acid values above 0.05 mg KOH/g can promote calcium-zinc stabilizer precipitation on die surfaces. Supplier lot acceptance therefore includes acid number, moisture, and ester content limits before compounding. Profiles are cut and mitered for food cold-storage doors and pharmaceutical cold-chain cabinet sealing systems where repeated flexing at low temperature must occur without plasticizer exudation.
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Bluesail Dioctyl Sebacate (DOS) is the diester formed from 2-ethylhexanol and sebacic acid, CAS 122-62-3, molecular formula C₂₆H₅₀O₄, molecular weight 426.67 g/mol. The product is an aliphatic dibasic ester plasticizer supplied as a clear, water-white oily liquid. It is specified in flexible PVC, plastisol, and synthetic rubber compounds where low-temperature flexibility, low volatility, and absence of ortho-phthalate restrictions are required. The standard industrial grade is controlled for ester content not less than 99.0%, acid value not above 0.05 mg KOH/g, water content not above 0.10%, and Pt-Co color not above 30 APHA. Liquid-phase constants include density at 20 °C of 0.913–0.919 g/cm³, refractive index at 20 °C of 1.450–1.453, and Cleveland open-cup flash point not below 210 °C. Packaging is available in 200 L epoxy-lined drums, 950 kg composite IBCs, and bulk ISO tanks; hot-climate storage beyond 60 days uses nitrogen blanketing.
| Parameter | Specification limit | Test method |
|---|---|---|
| Appearance | Clear, water-white liquid | Visual inspection |
| Ester content | ≥ 99.0% | Gas chromatography / ASTM D1045 |
| Acid value | ≤ 0.05 mg KOH/g | ASTM D1045 |
| Water content | ≤ 0.10% | ASTM E203 |
| Color | ≤ 30 APHA | ASTM D1209 |
| Density at 20 °C | 0.913–0.919 g/cm³ | ASTM D4052 |
| Refractive index n20/D | 1.450–1.453 | ASTM D1218 |
| Flash point, Cleveland open cup | ≥ 210 °C | ASTM D92 |
Comparative plasticizer selection in flexible PVC is resolved by measuring torsional stiffness at low temperature. Under ASTM D1043, a 50 phr DOS-plasticized compound based on a medium-molecular-weight suspension PVC resin retains flexibility at a Clash-Berg Tf value 20–30 °C below that of an equivalent DOP or DINP control. The difference arises from the linear sebacate backbone; without aromatic ring stacking, polymer chain mobility remains higher at subzero temperatures. Against dioctyl adipate, DOS provides a longer C10 diacid segment, which reduces plasticizer loss in activated-carbon exposure at 85 °C for 24 h according to ISO 176 and lowers soapy-water extraction at 50 °C. The trade-off is higher melt viscosity and higher cost per kilogram; for this reason formulators commonly use DOS at 15–35 phr as a low-temperature flexibilizer in DINP or trimellitate primary systems. Direct substitution at equal Shore A hardness is not linear because hardness response depends on filler type, stabilizer package, and resin K-value. When a compound must avoid ortho-phthalate restrictions while retaining subzero flexibility, DOS is introduced as a partial replacement rather than a full drop-in for DOP.
For PVC cable sheathing and insulation, dry-blend preparation follows a defined sequence. High-speed mixers with thermocouple control drop the formulation at 105–125 °C; the plasticizer is introduced after dry resin reaches 70–80 °C to prevent localized viscosity pockets. On co-rotating twin-screw extruders with L/D 44:1 compounding 70 °C-rated cable sheathing, barrel zones are set from 140 °C to 175 °C, and melt temperature at the die is held below 190 °C. A torque rheometer fusion curve under ASTM D2538 typically shows a 20–40 s delay in the torque peak for DOS compared with DOP at the same 50 phr loading, so operators increase the barrel setpoint by 5–10 °C or add 0.2–0.5 phr of acrylic processing aid. For plastisol operations, DOS lowers low-shear viscosity and extends bench life, but moisture levels above 0.10% must be reduced by vacuum deaeration at 20–30 kPa absolute before coating. Extended melt residence beyond 8 min above 200 °C is a documented processing boundary; acid-value drift and volatile condensate on downstream dies occur as the ester linkage begins to hydrolyze or thermally degrade. Output rates on 75 mm twin-screw lines producing cable sheathing are reported in the range 600–900 kg/h; torque stability within this window responds more to filler loading than to DOS ratio when DOS is held between 20–35 phr.
In nitrile rubber and chloroprene formulations, DOS functions as an aliphatic processing plasticizer. Addition levels of 5–15 phr are common for molded seals and automotive hoses that must pass low-temperature retraction tests under ASTM D1329. A DOS-plasticized NBR compound typically shows a Gehman torsion T10 by ASTM D1053 that is 10–15 °C lower than an equal phr DOP control; the effect is smaller in high-acrylonitrile grades because the nitrile polymer backbone contributes more low-temperature stiffening. In chloroprene, DOS lowers compound viscosity and improves release, but adverse interaction with amine-based antidegradants in high-humidity service can accelerate ester hydrolysis, so hydrolysis-resistant stabilizer packages are required. Extraction resistance should be checked by ISO 1817 in ASTM Oil No. 1 at 100 °C, because DOS remains extractable in non-polar service fluids. For automotive interior applications requiring low fogging, formulation-specific testing by ISO 6452 or SAE J1756 is necessary; published data for this specific configuration is limited, and lot-specific certificates are recommended.
The main operational limitation of DOS is its finite migration rate in contact with non-polar media and its susceptibility to hydrolysis at elevated moisture and temperature. In cable sheathing, extraction loss in detergent solutions is typically lower than dioctyl adipate but must be validated for each compound because stabilizer choice and filler loading influence the measured value. Regulatory compliance is not automatically conferred by the plasticizer alone; the finished article must be tested for overall migration under EU No 10/2011 and for specific migration where member-state legislation requires it. The substance appears in FDA 21 CFR 178.3740 as a plasticizer for polymeric materials; therefore, food-contact use requires confirmation that the specific Bluesail lot meets the referenced purity criteria and that the final polymer matrix does not exceed relevant migration limits. Under REACH Regulation (EC) 1907/2006 and CLP Regulation (EC) 1272/2008, the industrial grade is supplied with a Safety Data Sheet; the material is not an ortho-phthalate and is not covered by the Annex XVII restriction entries applicable to DEHP, DBP, BBP, or DIBP.
Storage and handling boundaries follow from the same ester chemistry. Bulk carbon steel tanks require desiccant breathers and over-temperature protection; the maximum bulk storage temperature is 40 °C, and hot-climate storage beyond 60 days benefits from nitrogen blanketing. Open steam coils should not be used because localized surface temperatures above 150 °C promote hydrolysis. The product is not classified as dangerous for transport under ADR/RID/IMDG, but spills should be contained with inert absorbent and excluded from watercourses. Prolonged contact with strong oxidizing agents and open flames must be avoided; thermal decomposition products include carbon oxides and low-molecular-weight carbonyl compounds.