| HS Code | 863610 |
| Productname | Kraton MD6459 |
| Polymertype | Styrene-butadiene-styrene (SBS) block copolymer |
| Structure | Linear triblock |
| Styrenecontent | 30 wt% |
| Butadienecontent | 70 wt% |
| Specificgravity | 0.94 |
| Meltflowrate | 11 g/10 min at 200°C/5 kg |
| Shoreahardness | 65 |
| Tensilestrength | 32 MPa |
| Elongationatbreak | 800% |
| 300 Modulus | 2.8 MPa |
| Brookfieldviscosity | approx. 1,800 cP at 25% in toluene |
| Volatilematter | <0.5 wt% |
| Antioxidant | Present |
| Appearance | White crumb or pellet |
As an accredited Kraton Kraton MD SBS MD6459 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton MD SBS MD6459 is supplied in 25 kg moisture-resistant paper bags, palletized for industrial handling and storage. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with Kraton MD SBS MD6459, securely stowed and sealed for international shipment. |
| Shipping | Kraton MD SBS MD6459 is shipped as a non-hazardous polymer in sealed bags or containers. It is not classified as dangerous goods for transport. Store and transport in a cool, dry, well-ventilated area, away from moisture, direct sunlight, and heat; keep containers closed. |
| Storage | Store Kraton MD SBS MD6459 in a cool, dry, well-ventilated area away from direct sunlight, heat, flames, and strong oxidizing agents. Keep containers tightly closed and labeled, protect from moisture and contamination, and avoid dust generation. Use good housekeeping; refer to the supplier’s SDS and local regulations for specific storage and handling requirements. |
| Shelf Life | Kraton MD6459 typically has a 24-month shelf life when stored cool, dry, and in unopened original packaging. |
Kraton MD6459 is a styrene-butadiene-styrene block copolymer in which polystyrene end-blocks aggregate into glassy domains that act as physical crosslinks, while the unsaturated polybutadiene midblock provides elastomeric recovery at service temperatures. The polymer is supplied as free-flowing porous pellets and should be dried at 70 °C for 2 h when storage relative humidity exceeds 60 %. Melt processing should not exceed 220 °C for prolonged hold-up because the butadiene segment undergoes thermal-oxidative chain scission and crosslinking. Finished-part compliance is controlled by the downstream formulation; the neat polymer alone does not confer food-contact, medical, or outdoor weatherability certifications.
Footwear outsole compounds use MD6459 as the elastic network in a hard phase of general-purpose polystyrene. A paraffinic or naphthenic oil is added to reduce hardness and improve melt flow. The compounding sequence on a co-rotating twin-screw extruder with L/D 40:1 begins with pellet feeding at the main throat and oil injection after the melting zone, at barrel segment 4 or 5. Barrel settings from feed to die are 150 °C, 170 °C, 180 °C, 190 °C, and 185 °C. Screw speed is set to maintain specific mechanical energy input of 0.18 kWh/kg to 0.24 kWh/kg; lower energy input yields visible gel particles in molded soles. The compound is injection molded at a melt temperature of 175 °C to 205 °C and a mold temperature of 25 °C to 50 °C. Mold temperatures below 15 °C produce flow marks at the gate. Table 1 lists a formulation gradient evaluated to identify the property cliff-edge at high oil loading.
| MD6459 (wt%) | GPPS (wt%) | Naphthenic oil (wt%) | Shore A | Tensile strength (MPa) | Tear strength (kN/m) | DIN ISO 4649 abrasion (mm³) |
|---|---|---|---|---|---|---|
| 30 | 50 | 20 | 72 | 11.5 | 27 | 130 |
| 35 | 40 | 25 | 65 | 8.8 | 25 | 165 |
| 40 | 30 | 30 | 55 | 6.2 | 22 | 210 |
| 45 | 20 | 35 | 45 | 3.9 | 18 | 280 |
Quality control for outsole compounds follows ISO 37:2017 tensile properties, ASTM D2240 hardness, ASTM D624 tear strength, DIN ISO 4649 abrasion loss, and ASTM D1052 Ross flex cut growth. For European supply, the compound must be accompanied by REACH registration data for the polymer, oil, and stabilizer package. Children’s footwear components require heavy metal release testing under EN 71-3. Exudation is controlled by limiting oil content to below the absorption capacity of the polybutadiene phase; representative compounds with oil above 35 wt% show surface bloom after 7 days at 60 °C. Amine-based stabilizers used in some nitrile rubber compounds should be avoided because they can accelerate odor formation in SBS footwear compounds. End products include dual-density sports shoe outsoles, casual shoe soles, and abrasion-resistant heel inserts.
In polymer-modified bitumen production, MD6459 is added at 3 wt% to 6 wt% of total binder. The bitumen is preheated to 180 °C and sheared with a rotor-stator mill. Tip speed is maintained at 15 m/s to 25 m/s. High-shear mixing continues for 45 min to 120 min; the endpoint is determined by fluorescent microscopy, where the SBS phase should display a continuous interlocked network rather than dispersed globules. The blend is transferred to an agitated low-shear tank at 160 °C to 180 °C. Storage stability is measured according to EN 13399 by comparing softening point values from the top and bottom of a 72 h vertical tube at 180 °C. A separation greater than 5 °C is unacceptable for terminal storage; reactive sulfur at 0.1 wt% to 0.3 wt% is used to form sulfide bridges that suppress gross phase separation. Sulfur addition above 0.5 wt% can produce gel particles and viscosity spikes. Polyphosphoric acid modification should not be combined with high SBS loading without phase inversion testing, because acid interaction can precipitate asphaltene domains and destabilize the SBS network. End products include road asphalt binders, bridge deck waterproofing sheets, and stress-absorbing membrane interlayers. Performance grading after short-term and long-term aging is conducted under AASHTO M320, ASTM D2872, and ASTM D6521. Published data for the exact dispersion index of MD6459 in high-viscosity asphalt grades is limited, so terminal trials should establish minimum shear time for each bitumen source.
Hot-melt pressure-sensitive adhesive production with MD6459 is carried out in a heated sigma-blade mixer or a vertical close-clearance mixer with jacketed temperature control. The polymer is blended with a hydrogenated hydrocarbon tackifier and white mineral oil. A starting formulation contains 25 wt% MD6459, 50 wt% tackifier, and 25 wt% oil. Mixing is performed at 160 °C to 180 °C; temperatures above 190 °C produce visible yellowing and a distinct odor. The tackifier is added after the polymer reaches melt phase to avoid mixer torque spikes; oil is added in three increments after each tackifier addition. The hot-melt is coated onto polyester film or biaxially oriented polypropylene via slot die at 170 °C to 185 °C. Viscosity is measured by ASTM D3236 at 177 °C, loop tack by PSTC-16, 180° peel adhesion on stainless steel by PSTC-101, and shear adhesion failure temperature by ASTM D4498. For food-packaging adhesives, end-use compliance is limited to formulations meeting 21 CFR 175.105; migration testing must be completed with the exact substrate and food simulant. End products include box-sealing tapes, protective films, and hygiene construction adhesives. Aromatic hydrocarbon solvents swell the polystyrene domains and should not be used in cleaning the coating line. Storage of finished rolls at temperatures above 40 °C can cause adhesive bleed at the edges. Published viscosity-shear-rate data for MD6459-specific hot melts are limited; pilot coater trials with the exact tackifier lot are required before slot-die coat weight is fixed.
Compounding MD6459 into polypropylene for impact modification is performed on a co-rotating twin-screw extruder configured with L/D 40:1. Polypropylene is fed at the main throat; MD6459 is introduced through a side feeder after the PP has melted to limit heat history in the high-viscosity melt. Maleic anhydride-grafted polypropylene at 2 wt% to 5 wt% improves interfacial adhesion between the dispersed SBS domains and the PP matrix. The melt temperature is maintained between 185 °C and 215 °C, with screw speed from 300 rpm to 600 rpm. At MD6459 loading from 5 wt% to 15 wt%, notched Izod impact strength measured under ISO 180/A at 23 °C increases, while flexural modulus measured under ISO 178 decreases. Loading above 20 wt% may create elongated co-continuous structures and delamination in injection-molded parts. End products include refrigerator interior panels, tool cases, and battery housings. Long-term heat stability is tested under ISO 188 at 100 °C to 120 °C. Outdoor use requires UV stabilization; accelerated weathering is performed according to ISO 4892-2, and the technical bulletin should state failure criteria for color change and retained tensile strength. REACH and 2011/65/EU RoHS apply to electrical and electronic enclosures.
Soft-touch hand tools and appliance grips are injection molded from MD6459 compounds with Shore A hardness from 40 to 60. The pellet is dried at 70 °C for 2 h when the packaging has been opened in ambient humidity. Injection molding uses a general-purpose screw with a compression ratio of 2.0:1 to 2.5:1 and a shut-off nozzle to prevent drool. Melt temperature is set at 175 °C to 195 °C; barrel residence time should not exceed 5 minutes at melt temperature. Overmolded polypropylene substrates are pre-treated by flame or atmospheric plasma; adhesion is checked by cross-cut test according to ISO 2409. Formulation for overmolding typically contains 25 wt% to 35 wt% MD6459, 15 wt% to 25 wt% styrene-modified aliphatic oil, and 40 wt% to 60 wt% high-melt-strength polypropylene. Silicone additives are limited to 0.5 wt% because higher levels cause surface haze. End products include drill housing grips, kitchen utensil handles, and power-tool secondary surfaces. For skin-contact consumer articles, the finished compound must comply with REACH Annex XVII entries for polycyclic aromatic hydrocarbons and phthalates.
Sheet extrusion lines running MD6459 compounds are configured with a barrier screw, a melt pump, and a flex-lip die. A compound for thermoformed trays uses 30 wt% MD6459, 20 wt% general-purpose polystyrene, 35 wt% high-impact polystyrene, and 15 wt% white mineral oil. The die melt temperature is 180 °C to 205 °C. Roll-stack temperatures are set to 90 °C top, 80 °C middle, and 60 °C bottom. Thermoforming is performed when sheet surface temperature reaches 110 °C to 130 °C. The window is narrow: below 105 °C the sheet tears at plug corners; above 135 °C bubbles and wall thinning occur. The plug assist speed is increased relative to PP sheet because MD6459 compounds have lower melt strength. End products include dunnage trays, equipment covers, and electronics packaging sleeves. Dimensional stability is measured under ISO 75-2 at 0.45 MPa. For shipments into electronics, the sheet must satisfy 2011/65/EU RoHS for cadmium, lead, mercury, and hexavalent chromium. Formed trays should not be stored in contact with aromatic hydrocarbon cleaners because the polystyrene domains can be attacked.
| Downstream process | Critical reference method | Typical specification or process limit |
|---|---|---|
| Footwear outsole injection molding | DIN ISO 4649 / ISO 37:2017 | Abrasion loss < 200 mm³; tensile strength ≥ 8 MPa at 35 wt% MD6459 |
| Bitumen modification | EN 13399 / AASHTO M320 | Softening point separation < 5 °C after 72 h at 180 °C |
| Hot-melt PSA coating | ASTM D3236 / PSTC-101 | Brookfield viscosity 3,000–15,000 mPa·s at 177 °C; peel adhesion on stainless steel ≥ 5 N/25 mm |
| PP impact modification | ISO 180/A / ISO 178 | Notched Izod increase without flexural modulus loss exceeding 20 % |
| Soft-touch overmolding | ISO 2409 / ISO 7619-1 | Cross-cut adhesion ≤ grade 2; Shore A 40–60 |
| Thermoforming low-durometer sheet | ISO 75-2 / 2011/65/EU | Sheet surface temperature 110–130 °C; HDT ≥ 45 °C at 0.45 MPa |
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The designation Kraton Kraton MD SBS MD6459 (hereafter MD6459) identifies a styrene-butadiene-styrene block copolymer supplied as low-dust pellets. The molecular architecture consists of two glassy polystyrene end blocks connected through an unsaturated polybutadiene midblock. Polystyrene domains phase-separate from the butadiene matrix and function as physical crosslinks, producing elastomeric recovery without vulcanization. The product code MD6459 belongs to the SBS class of thermoplastic elastomers and is not a hydrogenated SEBS or an isoprene-based SIS grade. Release testing for this material typically includes melt mass-flow rate by ISO 1133-1:2022 at 200 °C with 5 kg load, density by ISO 1183-1:2019, Type A hardness by ASTM D2240-15e1, tensile properties by ISO 37:2017, Vicat softening temperature by ISO 306:2022, and moisture by ISO 15512:2019. Bound styrene content, diblock content, and molecular weight distribution are lot-specific values determined by gel permeation chromatography and nuclear magnetic resonance spectroscopy; they appear on the certificate of analysis. Because published consolidated values for every MD6459 lot are limited, incoming inspection should use the shipment-specific certificate rather than class-wide design values.
The polystyrene endblock glass transition in unplasticized SBS compounds is commonly observed near 95–100 °C by dynamic mechanical analysis under ISO 6721-1:2019 at 1 Hz. The polybutadiene midblock transition occurs below -70 °C, providing low-temperature flexibility. Microphase-separated domain spacing for styrenic triblock copolymers of this molecular weight class typically falls between 20 nm and 50 nm and can be confirmed by small-angle X-ray scattering or atomic force microscopy. The physical crosslink network remains effective only while the polystyrene domains remain glassy and intact; prolonged creep at temperatures above 90 °C may produce permanent set. This behavior distinguishes MD6459 from thermoset vulcanizates, which rely on irreversible chemical crosslinks, and from hydrogenated SEBS grades, which are more stable toward oxidative degradation but still retain the same styrenic endblock service limit.
The unsaturated polybutadiene midblock is the critical thermostability limitation. Under accelerated oven aging at 70 °C per ISO 188:2023, unhydrogenated SBS compounds can lose elongation through allylic oxidation, chain scission, and crosslinking. Melt processing accelerates these reactions; melt temperature should remain below 190 °C, and residence time above 190 °C should not exceed 5 min. In a co-rotating twin-screw extruder with L/D 40:1, barrel temperatures from feed to die are commonly set from 130 °C to 180 °C. Specific mechanical energy should be held below 0.20 kWh/kg; aggressive kneading can create localized shear heating that forms gel particles detectable as pressure rise across a 14 µm screen pack. Predrying is required when moisture determined by ISO 15512:2019 exceeds 0.10 wt%. A desiccant dryer operating at 70–80 °C for 2 h with a dew point below -30 °C removes surface moisture. In hot-melt coating or bulk melt holding, the melt bath should be nitrogen-blanketed if held above 160 °C for more than 30 min. Amine-based stabilizers in unpigmented MD6459 compounds require bloom and staining tests because low-molecular-weight amine species can migrate to the surface and alter tack or color.
Single-screw extrusion requires a three-zone screw with L/D 24:1–30:1 and compression ratio 2.5:1–3.5:1. Barrel temperatures from 150 °C to 180 °C are typical for unfilled compounds. Die design must account for high die swell and relatively low melt strength compared with flexible PVC; drawdown ratios between 1.5:1 and 3:1 are practical starting points. Injection molding uses a shut-off nozzle to prevent drool, barrel zones from 150 °C to 190 °C, mold temperature from 30 °C to 60 °C, and back pressure below 0.5 MPa. Holding pressure is commonly 50–70% of peak injection pressure. Shrinkage is anisotropic and generally falls from 0.8% to 1.5%, depending on filler content, gate type, and molecular orientation.
Rheological characterization of MD6459 compounds at 180 °C by capillary rheometry across shear rates from 10 s⁻¹ to 1000 s⁻¹ typically shows pseudoplastic flow because the styrenic endblock domains orient under shear. Apparent viscosity below 10 Pa·s at the coat temperature is often required for continuous hot-melt slot-die transfer; profile extrusion compounds can generate die pressures near 15 MPa depending on die restriction. Batch-to-batch variance in melt flow rate should be compared against the certificate of analysis before adjusting screw speed or barrel temperatures. Screen-pack pressure rise is monitored during extrusion, but the acceptance threshold is set by the production facility because published process limits for this grade are limited.
When MD6459 is used in hot-melt pressure-sensitive adhesives, the formulation comprises the SBS, a hydrocarbon tackifier, and a naphthenic or paraffinic process oil. The polymer supplies cohesive strength and elastic recovery; the tackifier raises glass transition temperature and wets the substrate; the oil reduces application viscosity. Because published peel values for this specific configuration are limited, screening should measure loop tack by ASTM D6195-03(2019), peel adhesion by ASTM D3330/D3330M-04(2018), and shear adhesion failure temperature by ASTM D3654/D3654M-06(2019). Slot-die coating at coat weights from 15 g/m² to 50 g/m² should be performed with heated hose and die at 160–175 °C. Higher resin levels increase tack and peel but reduce shear holding power; higher oil levels reduce viscosity and shear resistance. SBS grades are selected over SIS when room-temperature shear holding and lower formulation cost are more important than low-temperature tack and softness.
The following matrix summarizes methods used to define the release envelope for MD6459 without substituting for the certificate of analysis.
| Property | Test Method | Measurement Condition |
|---|---|---|
| Melt mass-flow rate | ISO 1133-1:2022 | 200 °C, 5 kg, die 2.095 mm |
| Density | ISO 1183-1:2019 | Immersion method, 23 °C |
| Hardness | ASTM D2240-15e1 | Type A, 15 s delay |
| Tensile stress at break | ISO 37:2017 | Type 2 dumbbell, 500 mm/min |
| Vicat softening temperature | ISO 306:2022 | Method A50, 10 N, 50 K/h |
| Moisture | ISO 15512:2019 | Karl Fischer coulometric |
| Accelerated heat aging | ISO 188:2023 | 70 °C, air oven |
| Dynamic mechanical analysis | ISO 6721-1:2019 | 1 Hz, -100 °C to 150 °C |
Class-level differences among unsaturated SBS, hydrogenated SEBS, and isoprene-based SIS arise mainly from midblock chemistry and saturation. MD6459 has carbon-carbon double bonds in the butadiene midblock; SEBS has a hydrogenated midblock that imparts higher oxidative aging resistance and permits higher processing temperatures, typically 220–260 °C, but also reduces compatibility with some hydrocarbon tackifiers and increases cost. SIS contains an isoprene midblock with a lower glass transition temperature and greater softness, making it common in low-temperature tapes and labels; SBS grades such as MD6459 are preferred where higher heat distortion resistance and tensile strength are required at moderate formulation cost. Within SBS, molecular architecture—linear versus radial, bound styrene content, diblock content, and molecular weight distribution—controls melt viscosity, hardness, tensile strength, and low-temperature flexibility. Higher bound styrene increases hardness and modulus but reduces low-temperature impact; higher diblock content assists wetting and reduces melt viscosity but may lower tensile strength and creep resistance.
| Polymer Class | Midblock Unsaturation | Typical Melt Processing Range | Oxidative Aging Resistance | Typical Shore A Range | Test Reference |
|---|---|---|---|---|---|
| MD6459 SBS | Unsaturated butadiene | 150–190 °C | Moderate | 45–95 | ASTM D2240-15e1 |
| SEBS | Hydrogenated midblock | 220–260 °C | High | 40–90 | ASTM D2240-15e1 |
| SIS | Unsaturated isoprene | 150–180 °C | Moderate to low | 30–80 | ASTM D2240-15e1 |
Commercial SBS products in this class generally span bound styrene from 10 wt% to 40 wt%, density from 0.93 g/cm³ to 0.95 g/cm³, Shore A hardness from 45 to 95, and melt mass-flow rate from below 1 g/10 min to above 50 g/10 min at 200 °C/5 kg. A processor moving from a radial SBS to MD6459 may observe lower melt strength and lower die swell if MD6459 has lower molecular weight or branching than the reference product. A formulator moving from a high-styrene SBS to MD6459 should expect lower hardness and Vicat softening temperature if the certificate confirms lower bound styrene. Conversely, if the MD6459 lot has higher diblock content than a reference grade, hot-melt wetting may improve while tensile strength may decline. Published data for this specific configuration is limited; comparative trials must use the actual certificate values for both products and identical test conditions under ISO 37:2017 and ISO 1133-1:2022.
MD6459 also functions as a modifier for polystyrene and polyolefin compounds. At addition levels from 5 wt% to 20 wt%, SBS can improve impact toughness and reduce stiffness in styrenic blends. Twin-screw dispersion requires distributive mixing with neutral kneading elements rather than high-intensity shear to avoid degrading the butadiene midblock. The modifier domain size should be assessed by scanning electron microscopy on fracture surfaces; domain sizes below 1 µm are generally required for effective impact modification, but published data for this specific configuration is limited. Compatibility with polypropylene and polyethylene is limited without a block or graft compatibilizer; phase morphology and interfacial adhesion determine final impact and tensile properties.
Modified bitumen formulations are another use area for MD6459. A high-shear mixer operating at binder temperatures of 170–180 °C disperses the polymer into the bitumen at addition levels from 3 wt% to 6 wt%. Mixing time depends on rotor tip speed, commonly 20–25 m/s, and batch geometry. Softening point is measured by ASTM D36/D36M-14(2020), penetration by ASTM D5/D5M-19a, elastic recovery by ASTM D6084/D6084M-21, and dynamic rheological response by ASTM D7175-23. Storage stability is determined by EN 13399:2017 after oven conditioning; if phase separation exceeds specification, the maltene-phase compatibility can be adjusted with aromatic process oil or polymer dosage reduced. Published field data for MD6459 in specific road binder grades is limited; binder development is empirical and depends on base bitumen composition and aggregate.
For footwear and general-purpose TPE compounds, MD6459 is mixed with crystal polystyrene, mineral oil, and silica or calcium carbonate in an internal mixer with chamber temperatures from 150 °C to 170 °C and rotor speeds from 35 rpm to 50 rpm. Discharge melt temperature is kept below 185 °C. Injection molding uses barrel zones from 150 °C to 190 °C and mold temperature from 30 °C to 60 °C. Cavity pressure for filled compounds is typically 25–40 MPa, and shrinkage ranges from 0.8% to 1.5%. Formulating with too much polystyrene increases hardness and melt viscosity but can reduce flex fatigue and low-temperature toughness; too much oil reduces tensile strength and may promote oil migration in service.
Storage and regulatory boundaries are defined by chemical resistance and unsaturation. MD6459 is swellable or soluble in aromatic hydrocarbons, chlorinated solvents, esters, and certain ketones; prolonged contact with these solvents destroys dimensional stability. Unstabilized thin sections are vulnerable to UV-induced embrittlement; outdoor service requires carbon black, titanium dioxide, or stabilizer concentrates. Food-contact, pharmaceutical, and medical use requires separate confirmation of regulatory status under FDA 21 CFR or EU 10/2011 before use. REACH Regulation EC 1907/2006 and RoHS Directive 2011/65/EU declarations are not implied by product availability and should be requested from the manufacturer. Avoid melt blending with strong oxidizing agents and strongly acidic additives; intentional addition of peroxides to the melt should be treated as controlled reactive extrusion only when chain modification is deliberately designed.