| HS Code | 570626 |
| Polymer Type | SEBS (styrene-ethylene-butylene-styrene) block copolymer |
| Structure | Linear triblock copolymer |
| Hydrogenation | Hydrogenated midblock |
| Styrene Content | 35 wt% |
| Diblock Content | <1 wt% |
| Physical Form | Powder |
| Color | White |
| Density | 0.91 g/cm³ |
| Bulk Density | 0.45 g/cm³ |
| Melt Flow Rate | 5 g/10 min (230°C/5 kg) |
| Shore A Hardness | 65 |
| Tensile Strength | 10 MPa |
| Elongation At Break | 600% |
| Vicat Softening Temperature | 65°C |
| Processing Temperature | 180-230°C |
As an accredited Kraton Kraton™A SEBS A1535 H factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ A SEBS A1535 H is supplied in 25 kg polyethylene-lined paper bags, with 40 bags per pallet (1,000 kg). |
| Container Loading (20′ FCL) | 20′ FCL loading: palletized Kraton A1535 H SEBS, evenly distributed, strapped securely, kept dry, within 20-foot container payload limits. |
| Shipping | Kraton™ A SEBS A1535 H is supplied as solid polymer pellets in moisture-resistant bags, boxes, or bulk containers. It is not classified as dangerous goods for transport (UN number not applicable) under DOT, IMDG, or IATA. Keep dry and store below recommended temperatures; avoid direct sunlight and excessive heat. |
| Storage | Store Kraton™ A SEBS A1535 H in a cool, dry, well-ventilated area in tightly closed original containers. Protect from direct sunlight, heat, moisture, and contamination. Keep away from ignition sources and strong oxidizing agents. Maintain ambient temperature and avoid prolonged storage above recommended limits. Follow local regulations and the manufacturer’s safety data sheet. |
| Shelf Life | Shelf Life: Typically 24 months from manufacture when kept in original sealed packaging under dry, cool, ambient conditions. |
When flexible PVC is removed from medical tubing specifications under hospital sustainability directives, SEBS A1535 H is introduced as the primary elastomeric phase in a polyolefin-rich compound. The material is supplied as a dense pellet with 100% triblock SEBS architecture, a styrene mass fraction of 58%, and a neat-polymer tensile strength of approximately 31 MPa when tested per ASTM D638-14. The compound is processed on a co-rotating twin-screw extruder with an L/D ratio of 40:1 to 52:1, configured with kneading blocks downstream of the feed zone and a vacuum vent at zone 8 of 10. Melt temperature at the die is maintained between 190°C and 220°C; localized shear heating above 240°C initiates viscosity degradation and gel speck formation that is detectable as surface defects in downstream tubing extrusion. Pre-drying at 70±5°C for 2–4 h is applied when ambient relative humidity exceeds 60%; failure to pre-dry produces splay and porosity in thin-walled tubing with wall thickness below 0.5 mm. Formulation loading for medical-grade compounds ranges from 45 wt% to 60 wt% A1535 H, with white mineral oil at 25–35 wt%, polypropylene homopolymer at 10–18 wt%, and a hindered phenolic/phosphite antioxidant package at 0.1–0.3 phr. The oil is side-stuffed into the melt zone rather than dry-blended with the pellets, because oil wetting in the feed throat causes screw slip and pressure instability at barrel zone 4.
Downstream tubing extrusion uses a single-screw extruder with barrier screw geometry and a compression ratio of 2.5:1 to 3.0:1, a screen pack of 60/80/100 mesh, and annular die temperatures held at 195–210°C. Calibration is performed in a vacuum sizing tank with water at 15–25°C; line speeds for 2–5 mm outside diameter tubing are typically limited by melt strength to 20–45 m/min. Post-crystallization hardness of the finished tube is Shore A 45 to Shore A 70 depending on oil loading. Sterilization compatibility is validated according to ISO 10993-5:2009 and ISO 10993-10:2010; gamma irradiation at 25–40 kGy is tolerated by the compound, while electron beam doses above 50 kGy may shift tensile elongation below 300%, a threshold documented in supplier technical bulletins for this grade class.
| Standard / regulation | Applicable clause / method | Verification target |
|---|---|---|
| FDA 21 CFR 177.1810(a) | Styrenic block copolymers for food contact | Extractives limits in n-heptane and aqueous media |
| USP <88> | Class VI biological reactivity | Systemic injection, intracutaneous, implantation |
| ISO 10993-5:2009 | In vitro cytotoxicity | Cell viability ≥70% |
| ISO 10993-10:2010 | Irritation and delayed-type hypersensitivity | No erythema / edema grade >1 |
| EU Regulation 10/2011 | Plastics food contact, overall migration | ≤10 mg/dm² |
| ISO 13485:2016 | Medical device QMS for compound production | Batch traceability, sterile packaging |
Terminal product types in this application segment include intravenous extension tubing, enteral feeding tubes, oxygen cannula tubing, wound drainage reservoirs, and peristaltic pump cassettes. The limiting factor for use in respiratory circuits is the softening effect of mineral oil migration into adjacent rigid components; initial oil bleed below 0.5% of compound mass after 72 h at 60°C is controlled by matching oil aromaticity and pour point to the EB midblock solubility parameter.
In closure lining operations, A1535 H is combined with ethylene-vinyl acetate, low-density polyethylene, and calcium carbonate to form a compressible sealing layer that must recover from closure torque without exceeding overall migration limits. The formulation contains A1535 H at 18–30 wt%, EVA with vinyl acetate content 12–18% at 10–20 wt%, LDPE or PP at 10–25 wt%, calcium carbonate at 10–30 wt%, and a foaming package based on sodium bicarbonate or azodicarbonamide at 0.5–1.5 wt%. The liner sheet is compounded on a twin-screw line with melt temperature 160–190°C, then calendered to a thickness of 0.4–1.2 mm and die-cut into discs. In the induction sealing step, foil-facing surface temperatures reach 180–230°C for 0.8–2.5 s; the liner must retain compression set below 40% after 22 h at 70°C per ASTM D395-18 to avoid leakage during repeated open-close cycles. Compliance is evaluated against FDA 21 CFR 177.1810(a), EU Regulation 10/2011 with overall migration below 10 mg/dm², GB 4806.6-2016, REACH EC 1907/2006, and RoHS Directive 2011/65/EU. Terminal product types include crown cap liners, screw cap liners, press-on twist-off seals, and tamper-evident induction seals for edible oils, sauces, dairy products, and pharmaceutical syrups. The low molecular weight of A1535 H reduces melt viscosity in the calendering nip, but high shear rates above 1,200 s⁻¹ during film conversion may cause local viscosity heating and odor development in the final liner.
In multi-shot injection molding cells where a rigid polypropylene substrate is overmolded with a soft skin at Shore 25–45 A, A1535 H is formulated as the continuous elastomer phase to minimize peel failure at the weld line. Formulation ranges include A1535 H at 25–45 wt%, white mineral oil at 20–35 wt%, and PP homopolymer at 10–20 wt%; the addition of 2–5 wt% calcium carbonate is introduced only for matte surfaces but reduces interfacial adhesion by 15–25% when not offset by maleic anhydride-grafted PP at 1–3 wt%. Processing on a reciprocating-screw injection molding machine with clamp force from 800 kN to 2,500 kN requires melt temperature 180–220°C at the nozzle and mold temperature 20–40°C. Substrate surface temperature at the point of second-shot contact must remain above 100°C to enable melt interdiffusion; cold-weld delamination occurs when the substrate skin drops below that threshold before injection. The low-torque, high-flow characteristic of A1535 H permits filling of wall sections down to 0.5 mm without flash at parting lines, but venting must be enlarged to 0.02–0.05 mm to release volatile oil breakthrough. Compliance testing includes hardness per ASTM D2240-05, tensile properties per ASTM D638-14, and melt flow rate per ISO 1133-1:2022; regulatory documentation follows REACH EC 1907/2006 and RoHS Directive 2011/65/EU. Terminal product types in this segment include power tool grips, toothbrush handles, handheld device corner bumpers, and medical device housing overmolds. The primary failure observed on production lines is oil exudation on long cooling times above 30 s, which reduces adhesion if the part is ejected warm and stored under compression before 24 h of ambient conditioning.
Elastic films for hygiene laminates are produced by cast film extrusion of A1535 H blended with metallocene LLDPE and polypropylene. The formulation loading for A1535 H is 20–35 wt%, with mLLDPE at 40–60 wt%, PP homopolymer at 10–20 wt%, and a white masterbatch at 5–10 wt%; erucamide at 500–1,500 ppm is added as a slip and antiblock agent. The cast film line operates with melt temperature at the flat die of 200–240°C, die gap 0.5–1.0 mm, chill roll temperature 15–25°C, and line speed 150–350 m/min. Film thickness is controlled within 40–120 µm; gauge variation above ±5% creates localized blocking force peaks detected by ASTM D3354-15 as values exceeding 0.15 N/cm. Hysteresis behavior is measured by cyclic elongation to 100% per ASTM D882-18; below 20 wt% A1535 H, permanent set after 100% elongation exceeds 20%, which is generally unacceptable for elastic side panels. Above 35 wt% A1535 H, quench efficiency on the chill roll declines and blocking force rises exponentially, creating winding difficulties and film blocking in warehouse storage above 35°C. Compliance is assessed against REACH EC 1907/2006, RoHS Directive 2011/65/EU, and skin-sensitization protocols under ISO 10993-10:2010 where laminates are intended for extended skin contact. Terminal product types in this segment include elastic side panels, waistbands, fastening laminates for baby diapers, adult incontinence briefs, and feminine hygiene pads. The most common production bottleneck is die-line buildup from the white masterbatch; purging with an mLLDPE cast-film displacement agent every 8–12 h maintains film clarity and reduces edge trim waste below 3%.
In oil gel systems for cosmetic and prosthetic pressure distribution, A1535 H is dissolved into white mineral oil at 5–12 wt% on a high-shear disperser heated to 130–150°C under vacuum of -0.08 MPa to -0.095 MPa. The batch is held at top speed for 45–90 min with tip speed 8–15 m/s to ensure complete dissolution of the styrenic endblock domains; it is then cooled to 20–30°C at a controlled ramp of 0.5–1.0°C/min. Cooling rate directly affects gel modulus and tack; rapid cooling below 1.0°C/min produces softer gels with higher oil bleed, while slower cooling increases endblock association and raises Shore 00 values. Formulation loading is determined by the required penetration depth and compressive modulus. Compliance for cosmetic and pharmaceutical contact is evaluated under FDA 21 CFR 178.3620(a) for white mineral oil, FDA 21 CFR 177.1810(a) for the SEBS polymer, USP <88> where the gel undergoes biological reactivity screening, and EU Regulation 1223/2009 for cosmetic finished products. Terminal product types include breast prosthesis fillers, wound dressing gel pads, cosmetic gel masks, wheelchair cushions, and keyboard wrist rests. The limiting processing constraint is oxidative embrittlement when antioxidant loading falls below 0.05 wt%; gels processed above 170°C without vacuum degassing develop yellowing and an increase in oil bleed over 30 days.
| A1535 H loading (wt%) | White mineral oil (wt%) | Antioxidant system (wt%) | Cone penetration ISO 2137:2017 (0.1 mm) |
|---|---|---|---|
| 5 | 94.9 | 0.1 | 250–320 |
| 8 | 91.9 | 0.1 | 140–200 |
| 12 | 87.8 | 0.2 | 60–110 |
In polypropylene impact modification, A1535 H is melt-blended with PP homopolymer or impact copolymer at 5–15 wt% to raise low-temperature Izod impact resistance while maintaining a higher melt flow rate than equivalent EPDM-based blends at the same rubber content. Processing is performed on a twin-screw extruder with barrel temperatures from 200°C to 230°C and a melt temperature at the die of 215–235°C; talc at 10–20 wt% may be co-fed when flexural modulus above 1,200 MPa is required. Dispersion is assessed by scanning electron microscopy of cryo-fractured plaques; domain sizes below 2 µm are necessary for notch sensitivity reduction. The formulation window is constrained at the upper limit by flexural modulus decline below 600 MPa when A1535 H loading exceeds 15 wt%, which disqualifies the blend for structural interior trim. Compliance testing includes notched Izod impact per ASTM D256-10 at -20°C and -30°C, flexural properties per ASTM D790-17, and melt flow rate per ISO 1133-1:2022; automotive documentation follows IATF 16949:2016 and PPAP submission requirements. Terminal product types in this segment include automotive interior trim panels, battery tool housings, appliance housings, luggage shells, and a range of thin-walled injection molded articles subjected to cold-drop impact. Published data for this specific configuration is limited regarding the long-term retention of impact strength after thermal aging above 110°C, requiring application-specific oven testing before production release.
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Kraton™ A1535 H is a linear hydrogenated styrenic block copolymer of the SEBS type, supplied as pellets and characterized by a bound styrene content of approximately 56 wt% according to manufacturer structural assay. The product is used in compounding, polyolefin modification, and elastomeric components requiring elevated hardness, reduced elastomeric recovery, and higher modulus than conventional low-styrene SEBS grades. Unlike SEBS polymers containing 30 wt% styrene that form discrete polystyrene domains in an ethylene-butylene matrix, the high styrene loading moves the material toward phase co-continuity and increases modulus, surface hardness, and upper service temperature while reducing low-temperature flexibility and oil uptake. Specific gravity measured by ISO 1183-1 is approximately 1.00. Hardness measured by ISO 868 is commonly reported in the 88–92 Shore A range. All values are lot-dependent; the current certificate of analysis and the manufacturer product datasheet govern.
At 56 wt% bound styrene, published densities of 1.05 g/cm³ for the polystyrene endblock phase and 0.86 g/cm³ for the hydrogenated ethylene-butylene midblock phase give an estimated hard-phase volume fraction of approximately 0.51. At 30 wt% styrene the comparable estimate is approximately 0.23. The exact morphology depends on thermal history, shear history, and endblock molecular weight. Transmission electron microscopy of compression-molded plaques can show co-continuous or lamellar hard-phase structures, whereas injection-molded parts may show oriented domains frozen by rapid cooling. Dynamic mechanical analysis according to ASTM D7028 typically reveals a poly(ethylene-butylene) midblock glass transition near -40°C and a polystyrene endblock glass transition near 95°C. The high hard-phase volume fraction increases the rubber plateau modulus and moves the material from a conventional elastomer toward a high-consistency, leathery elastomer. Molecular mass distribution can be monitored by ASTM D5296 gel permeation chromatography; endblock molecular weight drift is a common source of batch-to-batch variation in hardness and melt viscosity.
Tensile properties determined under ISO 37 are typically reported in the range of 30–33 MPa tensile strength and 430–480% elongation at break for compression-molded test specimens. Hardness under ASTM D2240 is commonly reported at 89 Shore A. Tear resistance measured by ISO 34-1 may be expected to be lower than that of a low-styrene SEBS with the same total molecular weight because the higher hard-phase continuity reduces energy dissipation through chain orientation in the elastomer phase. The product’s higher polystyrene content also raises the stiffness-temperature coefficient; heat resistance is improved, but low-temperature flexibility is reduced. Comparative values for a typical lower-styrene SEBS are given in the table below.
| Parameter | High-styrene A1535 H | Lower-styrene SEBS reference | Method or basis |
|---|---|---|---|
| Bound styrene | 56 wt% | 30 wt% | Manufacturer structural assay |
| Estimated hard-phase volume fraction | 0.51 | 0.23 | Calculated from phase densities |
| Hardness | 89 Shore A | 72 Shore A | ASTM D2240 |
| Tensile strength | 30–33 MPa | 28 MPa | ISO 37 |
| Elongation at break | 430–480% | 500% | ISO 37 |
Compounding of Kraton™ A1535 H is typically run on co-rotating twin-screw extruders with an L/D of 40:1 and side-stuffer capability for oil or filler addition. Barrel profiles are generally set in the 150–220°C range depending on screw speed, feed rate, and pelletizing configuration. Melt temperature measured at the die adaptor should not remain above 230°C for extended periods because the hydrogenated midblock can undergo chain scission and the polystyrene endblock can thermo-oxidatively degrade. Production-scale compounding lines show that strand pelletizing stability deteriorates when melt temperature approaches 235°C; the observed failure mode is strand fusion in the water slide and pellet-tailing at the die face. Reducing screw speed by 20–30% and lowering the downstream barrel zones by 10–15°C generally restores strand integrity. Pre-drying in a desiccant dryer with a dew point below -40°C at 80°C for 2–3 h is recommended when pellet moisture is visible or ambient relative humidity exceeds 60%; residual moisture should be controlled below 0.05 wt% as measured by ISO 15512 or an equivalent Karl Fischer procedure.
During injection molding, capillary rheometry data generated under ISO 11443 should be used for mold-filling simulation. Commercial processing often uses barrel temperatures from 190°C to 220°C and injection pressures of 50–100 MPa. Clamping force should be calculated from projected area multiplied by cavity pressure; thin-wall articles commonly develop cavity pressures of 40–60 MPa. Hot-runner systems should minimize dead spots, and shutdown purging with a lower-viscosity polypropylene or polyethylene grade reduces stagnation of the high-styrene melt in the manifold. Mold release may require higher ejection forces than a lower-hardness SEBS because of the product’s increased modulus; tooling trials should quantify ejection force by load-cell monitoring rather than by feel.
Addition of Kraton™ A1535 H to isotactic polypropylene at 10–30 wt% raises notched impact resistance as measured by ISO 179-1 and reduces flexural modulus as measured by ISO 178. The phase morphology shifts from dispersed elastomer droplets toward co-continuous structures near the 30 wt% loading, producing measurable changes in melt elasticity and die swell. On a 40:1 L/D co-rotating twin-screw extruder, the SEBS is fed through a loss-in-weight gravimetric feeder into the main feed throat; the screw configuration should emphasize distributive mixing zones rather than high-intensity kneading blocks to avoid excessive frictional heating. Specific energy input in the 0.20–0.30 kWh/kg range is commonly targeted for uniform dispersion; published data for this specific grade configuration is limited, so confirmation by scanning electron microscopy of cryofractured specimens is recommended. Formulators adjust phase morphology by controlling cooling rate and by adding olefinic block compatibilizers; instrumented Charpy tests at 0°C and -20°C are used to detect ductile-to-brittle transitions.
Elastomeric overmolding onto polycarbonate/ABS substrates is a relevant application when adhesion is verified using ASTM D903 peel testing or ISO 8510-2 cross-cut testing. The Shore A hardness of approximately 89 measured by ASTM D2240 provides a harder surface than low-styrene SEBS overmolding grades. Because the midblock is hydrogenated, oxidative stability is superior to unsaturated SBS and SIS alternates; accelerated aging per ISO 188 at 70°C for 168 h can screen antioxidant packages. Medical device components can be considered only when final-device biological evaluation under ISO 10993-1 is completed; raw-polymer certification does not replace finished-device validation.
Replacement of a conventional SEBS with 30 wt% bound styrene by Kraton™ A1535 H changes part hardness from approximately 72 Shore A to 89 Shore A under ASTM D2240, reduces elongation at break from approximately 500% to 450% under ASTM D412, and increases modulus. Existing tools designed for lower-hardness grades may require adjustment of gate dimensions, venting, and ejection because the harder grade generates different cavity-pressure profiles and shrinkage characteristics. Mold shrinkage should be measured according to ISO 294-4 after molding at the intended barrel temperatures and mold temperatures; conversion cannot be based solely on datasheet values. Melt viscosity is generally higher than that of a lower-styrene SEBS of comparable molecular weight; processing may require raising melt temperature by 10–20°C within the allowed 190–220°C range. The replacement condition should be evaluated by measuring Shore A hardness, tensile properties, and melt volume-flow rate on the same lot in the existing tool.
Limitations of A1535 H include lower oil retention than low-styrene SEBS grades. Aliphatic and paraffinic oils may be used in compounds, but high aromatic oils can plasticize the polystyrene hard phase and lower the upper service temperature. Compatibility with polar polymers such as polyurethanes, polyamides, and polyesters is low; adhesion to such substrates typically requires tie layers, surface activation, or reactive modification. The product should not be processed in contact with amine-based additives that may interfere with the antioxidant package or generate acid-base reaction products; published data for this specific interaction is limited. High-shear, long-residence processing above 230°C may cause yellowing and melt-viscosity drift. Free-radical peroxide modification should be controlled carefully because peroxide-induced crosslinking of the saturated midblock can create gel particles; screen-pack pressure rise across a 200 mesh screen can be used as a production-floor gel indicator.
Raw-polymer regulatory status is not a finished-article approval. The following matrix identifies the standards and references commonly cited for articles containing SEBS; each item must be confirmed for the final formulation and use condition.
| Regulatory domain | Reference | Verification requirement |
|---|---|---|
| Food-contact polymers, repetitive-use articles | FDA 21 CFR 177.1810 | End-use temperature, food type, and formulation limits must be confirmed against the supplier food-contact letter. |
| European chemical inventory compliance | REACH | Registration statement and substance volume tracking must be confirmed for the specific grade and import site. |
| Hazardous substances in electrical and electronic equipment | RoHS Directive 2011/65/EU | Cadmium, lead, mercury, hexavalent chromium, PBB, and PBDE must be below directive thresholds by test method IEC 62321. |
| Medical device biological evaluation | ISO 10993-1 | Cytotoxicity, irritation, and sensitization tests must be performed on the final sterilized device, not on the raw polymer alone. |
For technical substitutions in existing formulations, the relevant boundary is not a single datasheet value but the intersection of hardness, melt viscosity, mold shrinkage, adhesion, and regulatory status. Published data for certain application-specific configurations of Kraton™ A1535 H is limited; therefore, molded part performance should be verified by measuring the exact property set under the relevant ASTM, ISO, or FDA reference method before release.