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Kraton Kraton™G SEBS-Oil G4609 H

    • Product Name: Kraton Kraton™G SEBS-Oil G4609 H
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 740087
    Grade Kraton™ G SEBS-Oil G4609 H
    Polymer Type Hydrogenated styrene-ethylene/butylene-styrene (SEBS) block copolymer with plasticizing oil
    Styrene Content 33%
    Oil Content 20%
    Density 0.90 g/cm³
    Melt Flow Rate 20 g/10 min (230 °C/5 kg)
    Shore A Hardness 65
    Tensile Strength 20 MPa
    Elongation At Break 600%
    Modulus At 300 Elongation 3.5 MPa
    Tear Strength 35 kN/m
    Vicat Softening Point 50 °C
    Form Pellet
    Appearance Clear/transparent

    As an accredited Kraton Kraton™G SEBS-Oil G4609 H factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kraton™ G SEBS-Oil G4609 H is packaged in 25 kg moisture-resistant bags, palletized and labeled for safe industrial handling.
    Container Loading (20′ FCL) Kraton™G SEBS-Oil G4609 H is palletized, stretch-wrapped, and securely loaded into 20′ FCL dry containers for shipment.
    Shipping Kraton™ G SEBS-Oil G4609 H is not classified as dangerous goods for transport. No UN number, hazard class, or packing group applies. Ship in original sealed bags/pallets in dry, clean conditions, avoiding excessive heat, sunlight, and moisture; normal freight handling is acceptable.
    Storage Store Kraton™ G SEBS-Oil G4609 H in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and oxidizing materials. Keep original containers or bags sealed to prevent moisture, dust, and contamination. Avoid prolonged exposure to elevated temperatures and UV light. Palletize securely, do not crush, and follow first-in, first-out stock rotation.
    Shelf Life Shelf life is 24 months from date of manufacture when stored in original unopened packaging under dry, moderate-temperature conditions.
    Application of Kraton Kraton™G SEBS-Oil G4609 H

    Kraton™ G4609 H — Application Engineering Scenarios

    Application engineering reference for Kraton™ G4609 H, an oil-extended styrene-ethylene/butylene-styrene block copolymer supplied as free-flowing pellets for downstream compounding and conversion. The scenarios below are restricted to established downstream routes: thermoplastic elastomer compounding for soft-touch consumer and industrial goods, medical device components, automotive interior soft-skin and TPO modification, polypropylene impact modification, footwear and orthotic compounds, wire and cable jacketing, and appliance and food-processing gaskets. Numerical ranges are representative engineering bands for process development or production audit, not a substitute for certificate-of-analysis data or destination-market regulatory clearance.

    In co-rotating twin-screw compounding of polyolefin-rich TPE formulations, Kraton™ G4609 H is introduced as a pre-extended styrenic block copolymer pellet stream, while the separate oil injection port is reduced or eliminated. On production lines running a Coperion ZSK Mc18 twin-screw extruder with L/D ratio 40:1, feed barrel flooding occurs when the feeding zone is run at 100% capacity because the oil-extended pellet softens before the side stuffer zone; the standard correction is a starved feed condition at 60%–80% of maximum feeder throughput. The addition ratio in this segment typically places G4609 H at 30 wt%–55 wt% in the final compound, with polypropylene random copolymer at 5 wt%–20 wt% and supplementary white mineral oil capped at 0 wt%–15 wt% when lower Shore A values are required. Screw speed is normally held between 250 rpm and 450 rpm, with barrel temperatures 170 °C–210 °C and die pressure 3 MPa–7 MPa. In this range, the styrenic end-block domains remain intact at the die, which preserves tensile recovery and reduces die swell to a controllable 3%–8%. Compliance for consumer goods and tool handles references EU REACH Regulation (EC) No 1907/2006, particularly Annex XVII restrictions on polycyclic aromatic hydrocarbons, EU RoHS Directive 2011/65/EU for EEE-adjacent products, and IEC 62321-7-1:2015 for PAH screening. For food-handle applications, FDA 21 CFR 177.1810 and EU Regulation (EU) No 10/2011 require migration testing under the intended time and temperature conditions and food simulants. The validating laboratory protocol follows ISO 868 for Shore A hardness at 15 s, ISO 37:2017 for tensile strength and elongation, ISO 815-1:2014 for compression set at 23 °C and 70 °C, and ISO 1133-1:2022 for melt mass-flow rate at 230 °C and 2.16 kg. The terminal product range covers overmolded grips for power tools, hand tools, kitchen appliance handles, toothbrush handles, appliance vibration dampers, and soft-touch caps for personal-care packaging. A process note: pellet drying is normally unnecessary below 60% RH but becomes mandatory above 60% RH, with 70 °C–80 °C desiccant drying for 2 h–4 h to prevent splay in injection molding.

    Representative property response bands across laboratory formulations of G4609 H in polypropylene for soft-touch consumer compounds; values are typical validation ranges, not grade certificate data.
    Formulation G4609 H / random PP / external oilShore A after 15 s — ISO 868Tensile strength MPa — ISO 37Elongation at break % — ISO 37Compression set 23 °C / 72 h % — ISO 815-1
    30/50/2055–604.0–5.5650–75030–35
    45/45/1045–523.0–4.5700–80025–30
    55/45/035–422.0–3.5750–85020–25

    What Process-Safety Limits Govern Injection Molding of Oil-Extended SEBS in Medical Device Components?

    For disposable and reusable medical device subcomponents such as infusion pump elastomers, respiratory mask cushions, syringe tip shields, and overmolded compliance grips on surgical instruments, Kraton™ G4609 H is generally let down into a medical-grade polypropylene or metallocene polyethylene carrier. The addition ratio in this segment commonly occupies 35 wt%–60 wt% of the final compound, while supplementary white mineral oil is withheld or capped at 5 wt%–10 wt% to keep extractables within design targets. Compliance is anchored to ISO 10993-5:2009 for cytotoxicity by MEM elution, ISO 10993-10:2013 for skin sensitization and closed-patch irritation, USP Class VI under USP 88 for systemic injection and intracutaneous testing, and USP 661.1 for plastic packaging components.

    Injection molding on a production machine with clamp force between 80 t and 160 t requires melt temperatures of 190 °C–230 °C, mold temperatures of 20 °C–45 °C, and screw back pressure of 0.5 MPa–1.5 MPa. Above 240 °C, the oil-extended midblock begins to yellow and generates volatiles that alter extractables profiles and can force rejection in pharmaceutical packaging. Pre-drying in a desiccant dryer at 70 °C–80 °C for 2 h–4 h is enforced when ambient RH exceeds 60% or when storage has been unheated. A bottleneck observed in multi-cavity hot-runner tools is imbalanced gate freeze-off caused by a sharp viscosity drop when melt temperature exceeds 220 °C; the corrective action is gate diameter reduction to 0.8 mm–1.2 mm and independent hot-tip temperature control rather than higher injection pressure. Terminal products include overmolded grips on medication delivery pens, seal gaskets in wearable injectors, IV port closures, respirator mask cushions, and instrument handle overmolds. Sterilization by gamma irradiation above 25 kGy can shift tensile properties and discoloration, so post-sterilization validation to ISO 37 tensile strength and ISO 815 compression set on finished molded parts is required.

    An additional operational boundary is chemical compatibility: amine-based release agents, certain quaternary ammonium disinfectants, and strongly oxidizing sterilants may promote surface cracking or oil migration in this class of compounds. Published data for this specific grade under repeated autoclavation cycles is limited; therefore repeated autoclave use at 121 °C must be evaluated by finished-part dimensional stability and dynamic fatigue protocols specific to the device design.

    Compliance checklist matrix for downstream applications using Kraton™ G4609 H; confirm current standard editions and regional obligations before batch release.
    Application segmentPrimary regulatory instrumentMechanical / chemical test basisTypical data for batch dossier
    Soft-touch consumer / tool gripsREACH (EC) No 1907/2006, RoHS 2011/65/EUISO 868, ISO 37, ISO 815-1, ISO 1133-1Shore A, tensile, compression set, MFR
    Medical device componentsISO 10993-5, ISO 10993-10, USP 88, USP 661.1, FDA 21 CFR 177.1810ISO 37, ISO 815-1, extraction studiesCytotoxicity, tensile, compression set, extractables
    Automotive interiorVDA 278, VDA 270, ISO 12219-1ISO 868, ISO 37, DIN 75201VOC, fogging, odor, tensile retention
    PP impact modificationREACH, EU No 10/2011 if food contactISO 179-1, ISO 180, ASTM D256, ISO 75-2Notched impact, flex modulus, HDT
    Footwear / orthoticREACH Annex XVII, California Proposition 65ISO 20872, SATRA TM92, ISO 815, ISO 868Flex fatigue, slip resistance, Shore A, compression set
    Wire and cable jacketIEC 60332-1-2, UL 62, UL 94ISO 37, ISO 815, ISO 974Tensile, flame test, low-temperature brittleness
    Appliance / food processing gasketsEU No 10/2011, FDA 21 CFR 177.1810ISO 37, ISO 815-1, migration testingMigration, tensile, compression set

    Where automotive interior decoupling layers are produced on direct extrusion and vacuum thermoforming lines, Kraton™ G4609 H is incorporated into polypropylene-rich TPO compounds to reduce grain replication pressure and raise contoured-surface recovery after bending. The addition ratio in this segment is typically 20 wt%–40 wt% of the compound; higher loadings above 45 wt% can lead to visible gloss variation and lower mar resistance unless a high-crystalline PP layer is coextruded. Regulatory compliance for passenger-cabin materials must address VDA 278:2011 for VOC and semi-volatile organic compound emissions, VDA 270:2018 for odor, ISO 12219-1:2021 for interior air sampling, and DIN 75201:2011 for windshield fogging. The production route usually includes a twin-screw compounding pass at 190 °C–220 °C with vacuum devolatilization at -0.08 MPa to -0.10 MPa, followed by single-screw sheet extrusion and embossing and thermoforming. The extender oil fraction is the primary source of condensed VOC on the forming tool; embosser roll surface temperatures are therefore held at 25 °C–45 °C to control migration while maintaining grain depth. Terminal products include instrument panel soft skins, door trim laminates, center console side covers, floor mat backing, and HVAC seal foils. A shallow-zone note: flat-sheet thermoforming tools require pre-stretched blank temperatures at 160 °C–180 °C to avoid corner stress whitening in this class of compounds.

    When Polypropylene Impact Modification Requires a Pre-Extended SEBS Feedstock

    In compounding plants that modify polypropylene copolymers for sub-zero impact performance, Kraton™ G4609 H is introduced as a pre-extended impact modifier to reduce the oil absorption stage required by lower-molecular-weight SEBS powder. The addition ratio in this segment is generally restricted to 5 wt%–15 wt% in polypropylene homopolymer or random copolymer matrices, because higher loadings progressively depress flexural modulus and heat deflection temperature. The relevant mechanical test suite includes ISO 179-1 for Charpy notched impact, ISO 180 for Izod notched impact, ASTM D256-10 for instrumented impact correlation, ASTM D790-17 for flexural modulus, and ISO 75-2 for heat deflection temperature. The compounding process is normally carried out on a twin-screw extruder with L/D ratio 32:1–44:1, side-feeding of talc or impact copolymers, and melt temperatures of 200 °C–230 °C; screw design should use low-shear distributive mixing elements rather than aggressive kneading blocks to avoid destroying the styrenic domain network responsible for impact toughening. Terminal products include automotive trims, appliance housings, battery-box components, and logistics containers. A limitation often underestimated on compounding lines is batch-to-batch variation in oil load when the masterbatch hopper is not agitated; weight loss feeders with vertical hopper agitation are specified at 1 kg/h–50 kg/h to prevent segregation of fines and oil-rich pellets. Published data for this specific grade in unfilled PP impact modification is limited, so plant trials on notched impact at -30 °C, -10 °C, and 23 °C must be performed against a comparable non-oil-extended SEBS control to isolate oil effects from molecular weight effects.

    Unlike conventional dry SEBS grades that require extended oil absorption time in a heated high-shear mixer, Kraton™ G4609 H enters the footwear or orthotic compounding sequence with the extender oil already incorporated, which changes mixing sequence and shear input. In midsole and orthotic compounds, the grade is used at 25 wt%–50 wt% in blends with EVA, polyolefin elastomer, or PP; the EVA fraction is usually 20 wt%–40 wt%, and chemical blowing agents are added at 0.5 wt%–2.0 wt% for foamed formulations. Mechanical tests applied to this segment are ISO 20872:2018 for flexing endurance, SATRA TM92 for abrasion resistance, ISO 868 for Shore A hardness, and ISO 815 for compression set after flex fatigue. The mixing process uses an internal mixer or twin-screw extruder; hot-air or tunnel oven temperatures for crosslinking and curing are set between 150 °C and 175 °C, depending on peroxide or silane graft packages. Terminal products include orthotic insoles, sandal midsoles, shoe cushioning inserts, heel pads, and ankle-foot orthosis soft liners. An operational boundary is that oil-rich grades can reduce adhesion to solvent-based polyurethane adhesives; footwear lines must test peel strength to SATRA TM401 after roughening and primer treatment, and should not assume that standard halogenated primers will wet the surface reliably if the surface oil film is not removed by a solvent wipe or corona discharge at 0.5 kW–1.0 kW.

    Wire and Cable Jacket Compounds: Oil Retention, Flame Retardant Filler Loading, and Screw Feeding Consistency

    The use of oil-extended SEBS in flexible wire and cable jacketing is reserved for applications where low-temperature flexibility below -40 °C and silicone-free tactile properties are required in consumer electronics cords or industrial flexible trailing cables. Addition ratio of Kraton™ G4609 H in the polyolefin and fire-retardant matrix commonly falls between 20 wt% and 45 wt%, depending on whether the compound is a halogen-free flame retardant grade or a non-FR low-voltage insulation. The relevant compliance set includes IEC 60332-1-2:2015 for single-cable flame propagation, UL 62 for flexible cord, UL 94 for flammability classification at specified thicknesses, and ISO 974:2000 for low-temperature brittleness. In halogen-free compounds containing aluminum trihydroxide or magnesium dihydroxide at total filler loadings 50 wt%–65 wt%, the oil content in the pre-extended grade can reduce compounding torque but also lowers the limiting oxygen index; the blend therefore requires a synergistic phosphorus-nitrogen flame retardant package added at 3 wt%–8 wt% to maintain performance. Extrusion is performed on a single-screw extruder with a compression ratio of 2.5:1–3.5:1 and a temperature profile of 160 °C–200 °C; fine wire mesh breaker plates at 80 mesh or 100 mesh are used to trap any oil-rich pellet agglomerates. Terminal products include flexible appliance cords, headphone cables, industrial flexible trailing cables, and robotics cable jackets. A process limitation is that extended exposure to hot mineral oil in service can extract the extender oil and raise harness stiffness; this is an accepted operational boundary for dry-indoor applications and is not an approved substitute for oil-resistant nitrile or polyurethane jackets in hydraulic environments.

    Finished-Article Migration Testing Governs Food-Processing Gasket Formulation

    Gasket and sealing profiles in food-processing equipment, beverage dispensers, and appliance service parts combine repeated flex fatigue with contact with aqueous or fatty food simulants. In this segment, Kraton™ G4609 H is compounded at 40 wt%–60 wt% in a PP or LDPE carrier; supplementary white oil addition is restricted to 5 wt% or less to preserve fat-contact migration limits. Direct-article compliance is established under EU Regulation (EU) No 10/2011 using food simulants A, B, C, and D2 at time and temperature conditions selected from Annex III; FDA 21 CFR 177.1810 applies where the article is used in food contact, and 3-A Sanitary Standards may apply to specific dairy and meat processing gaskets. The production process commonly involves twin-screw compounding followed by injection molding or profile extrusion; mold temperature is kept at 25 °C–50 °C to minimize gate blush and sink marks, while the compound melt temperature is held at 190 °C–220 °C. Terminal products include drain hose gaskets, service door seals, blender base gaskets, espresso machine brew-unit seals, and food-plant door profiles. A quality audit point is that oil bloom on the sealing surface can reduce wet friction and cause seal chatter in potable water systems; surface wiping and hardness changes after 1,000 h water immersion at 60 °C should be checked against ISO 868 and ISO 37 before production release. Published data for this specific grade under high-fat food simulant D2 is limited, so migration testing must be performed on finished gaskets, not on raw pellets.

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    Certification & Compliance
    More Introduction

    Specification table and test designations

    Kraton™ G4609 H is a linear hydrogenated styrenic block copolymer (SEBS) supplied as a pelletized feedstock with a styrene/rubber ratio of 30/70. The polymer is a triblock architecture in which polystyrene end-blocks provide physical crosslinking at ambient temperature and the hydrogenated ethylene-butylene midblock remains saturated. The absence of midblock unsaturation gives oxidative and ultraviolet resistance relative to unhydrogenated SBS grades. Under ASTM D1238 at 230 °C/5 kg, the melt flow rate is 25 g/10 min. This flow rate places the product in the high-flow segment of SEBS grades and permits compounding at lower torque than high-molecular-weight analogues such as Kraton G1651 H on a 40:1 L/D twin-screw extruder. The product is used in soft-touch overmolding, sealants, adhesives, medical elastomers, and polymer modification where high oil acceptance and thin-wall filling are required. The supplier technical data sheet lists a tensile strength of 28 MPa, elongation at break of 500%, and Shore A hardness of 65 on compression-molded plaques tested according to ASTM D638 and ASTM D2240. The styrene domains remain phase-separated at service temperature and provide mechanical integrity without chemical vulcanization; this permits melt reprocessing and recyclability within the processor's established thermal limits.

    Table 1 consolidates typical values reported by the supplier for neat G4609 H. Determinations are performed on compression-molded plaques conditioned for 24 h at 23 °C/50% RH according to ASTM D618. The values are not batch-release minima; lot-to-lot variation is controlled by the supplier's internal specification limits. Melt flow rate is measured at 230 °C/5 kg using ASTM D1238. Tensile properties are measured on Type IV specimens at a crosshead speed of 500 mm/min; the reported values reflect the physical crosslink density of the polystyrene domains.

    Table 1. Typical physical properties of Kraton G4609 H
    PropertyTest methodValue
    Polystyrene contentSupplier method (FTIR)30% by mass
    Melt flow rateASTM D123825 g/10 min
    Specific gravityASTM D7920.91
    HardnessASTM D2240, Shore A, 10 s65
    Tensile strengthASTM D638, Type IV28 MPa
    Elongation at breakASTM D638, Type IV500%

    The phase morphology of G4609 H consists of spherical or cylindrical polystyrene domains dispersed in a continuous ethylene-butylene rubber phase when neat. The domain morphology depends on thermal history and solvent casting. In melt-processed compounds, the polystyrene domains act as multifunctional physical crosslinks. At temperatures above the glass transition of polystyrene, the domains soften and the polymer flows. This reversible network formation allows the material to be processed like a thermoplastic while retaining elastomeric recovery at service temperature. The service temperature ceiling is bounded by the glass transition temperature of polystyrene, which is approximately 95 °C; compounds under continuous load lose dimensional stability as the polystyrene domains soften.

    What limits oil acceptance in high-flow SEBS compounds?

    The oil acceptance of G4609 H is controlled by the interaction of the paraffinic oil with the ethylene-butylene midblock and by the physical network integrity of the polystyrene domains. Paraffinic white mineral oils with kinematic viscosity of 40–100 mm²/s at 40 °C are preferred because naphthenic or aromatic oils swell the polystyrene domains and reduce service temperature resistance. Oil is selectively solvated into the rubber phase during compounding; the polystyrene domains remain glassy and maintain the network. If oil addition exceeds the compatible loading for the styrene content and molecular weight, the rubber phase becomes saturated, the glass transition temperature of the midblock drops, and oil bleed or surface tack develops.

    The high-flow architecture of G4609 H has shorter chain length than G1651 H. This reduces entanglement density and lowers the maximum oil loading before network collapse. Published data for the oil bleeding threshold of this specific grade is limited; compounding trials at oil loadings above 120 phr generally require compatibility assessment by ASTM D5890 or a 7-day accelerated bloom test at 70 °C. In twin-screw extrusion, oil is injected downstream after polymer melting, typically at barrel 5–7 of a 40:1 L/D machine. Early oil injection causes screw slip, barrel pressure fluctuation, and melt temperature instability. The use of distributive mixing elements after oil injection improves dispersion but increases melt temperature.

    Because the product is non-functional, oil retention depends on physical encapsulation rather than chemical bonding. When oil retention is critical in skin-contact applications, the compounder may reduce oil loading, select a higher-molecular-weight SEBS, or add a microcrystalline wax to modify migration kinetics. G4609 H is supplied as a neat SEBS; oil is incorporated downstream during compounding, not as a pre-compounded oiled grade.

    When G4609 H replaces lower-flow grades in soft-touch injection molding

    Comparative data for selected SEBS grades are shown in Table 2. In thin-wall soft-touch overmolding, G4609 H reduces injection pressure and permits fill at lower melt temperature compared with G1650 M or G1651 H. The lower melt viscosity of G4609 H is beneficial for cavity fill in wall sections below 1 mm, but it also reduces shear heating during plastication. On a 1,200 kN injection molding machine with a 0.8 mm wall thickness, the high melt flow rate shortens hold-pressure time before gate freeze-off; however, the lower molecular weight reduces tensile strength relative to G1650 M. When G4609 H replaces G1650 M in a soft-touch compound, the formulator may need to increase filler or adjust oil level to maintain identical hardness because the lower melt viscosity reduces shear heating and can produce lower melt temperature at the same barrel setpoints.

    Table 2. Comparative data for selected neat SEBS grades
    GradeStyrene content (% mass)Melt flow rate (g/10 min, 230 °C/5 kg)Shore A hardnessTensile strength (MPa)Elongation at break (%)
    G4609 H30256528500
    G1650 M3057235500
    G1651 H30<16535500
    G1657 M13224523750

    The difference in styrene content between G4609 H and G1657 M is significant. The 30% styrene content of G4609 H produces higher hardness and modulus, but lower elongation and lower elastic recovery. In applications requiring low hardness with high elongation, G1657 M is selected despite lower styrene content. In applications requiring higher heat resistance and dimensional stability, G4609 H is selected because the higher polystyrene fraction raises the upper service temperature of the physical network. Compared with unhydrogenated SBS, the saturated midblock improves UV and oxidative stability but does not improve solvent resistance.

    Relative to Kraton FG1901 G, a maleic anhydride-functionalized SEBS, G4609 H contains no anhydride functionality. Therefore, G4609 H does not develop chemical adhesion to polyamides, polyesters, or metal surfaces during overmolding. Adhesion to polar substrates requires formulation with tackifiers or use of a functionalized grade. This lack of functionality also gives G4609 H broader compatibility with non-reactive hydrocarbon resins and paraffin oils. Compared with vulcanized rubber, the physical crosslinks of G4609 H provide lower continuous service temperature and higher compression set. The product is selected for reprocessability and design flexibility rather than for high-temperature compression-set resistance.

    Processing above 240 °C alters degradation kinetics

    Thermal degradation of SEBS occurs by chain scission and oxidation. At melt temperatures above 240 °C, degradation accelerates, leading to melt index drift, yellowing, and loss of tensile strength. The recommended melt temperature range for G4609 H is 190–230 °C. In twin-screw extrusion, barrel setpoints are profiled from 160 °C at feed to 220 °C at die. Nitrogen purging of the feed throat is used to reduce oxidative degradation at high screw speed. The product is not hygroscopic to the extent of condensation polymers, but storage at relative humidity above 60% may require drying at 80 °C for 2 h. The polymer is incompatible with aromatic solvents and strong oxidizing acids; toluene or xylene dissolves the polystyrene domains and causes irreversible loss of mechanical integrity. Chlorinated solvents should be avoided because they can promote midblock degradation in the presence of light.

    Supplier documentation lists the product for use in formulations that may be evaluated under FDA 21 CFR 177.1810 for styrene block copolymers in contact with food. The compounder is responsible for confirming specific migration limits and food-type conditions. Medical applications require formulation and sterilization validation according to ISO 10993-5 and ISO 11135 or equivalent. The product is supplied as a non-sterile pellet and does not itself constitute a medical device. For UV-stabilized compounds, a hindered amine light stabilizer system compatible with saturated rubbers is typically used; the unsaturated-free midblock reduces susceptibility to ultraviolet degradation. Because G4609 H is non-functional, adhesive formulations relying on polar substrate interaction should incorporate a compatible tackifier or use a maleated SEBS grade.

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