| HS Code | 272444 |
| Polymertype | SEBS (styrene-ethylene/butylene-styrene) |
| Polymerstructure | Linear triblock copolymer |
| Styrenecontent | 30 wt% |
| Form | Powder |
| Appearance | White powder |
| Specificgravity | 0.91 |
| Bulkdensity | 0.40 g/cm3 |
| Meltindex | 5 g/10 min at 230°C/5 kg |
| Shoreahardness | 70 |
| Tensilestrength | 30 MPa |
| Elongationatbreak | 600% |
| Modulus300percent | 5 MPa |
| Tearstrength | 30 kN/m |
| Volatiles | <0.5% |
| Ash | <0.2% |
| Antioxidant | Present |
As an accredited Kraton Kraton™G SEBS G1730 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ G SEBS G1730 is supplied in 25 kg multiwall paper bags, palletized for industrial handling and storage. |
| Container Loading (20′ FCL) | Kraton G1730 SEBS is loaded into a 20-foot FCL container, with pallets secured and moisture protection for safe overseas transport. |
| Shipping | Kraton™ G SEBS G1730 is shipped as non-hazardous thermoplastic elastomer pellets in moisture-barrier bags or boxes. It is not classified as dangerous goods for transport. Keep dry, away from direct sunlight and excessive heat, and avoid contamination; follow the SDS and label instructions. |
| Storage | Store in a cool, dry, well-ventilated area. Keep containers tightly closed and use original packaging. Protect from direct sunlight, heat, ignition sources, and strong oxidizing agents. Prevent moisture contamination, dust generation, and static discharge. Maintain good housekeeping and first-in, first-out stock rotation. Store away from food and drink. No special ventilation is required under normal handling conditions. |
| Shelf Life | Typically 24 months from date of manufacture when stored dry, sealed in original packaging at ambient temperature. |
Kraton™ G SEBS G1730, a linear styrene-ethylene/butylene-styrene block copolymer with 30 wt% bound styrene and a fully hydrogenated midblock, is melt-compounded into clear medical fluid-path formulations at addition levels of 30–55 wt%. The compound formulation pairs the SEBS with a medical-grade white mineral oil at 35–55 phr and a random copolymer polypropylene at 10–20 phr; the SEBS contributes the rubbery plateau modulus and conformability, while polypropylene raises the continuous-phase heat distortion temperature and suppresses oil bleed. Compounding is performed on a co-rotating twin-screw extruder with 40:1 L/D, vacuum devolatilization at −0.08 MPa, and a barrel temperature profile from 165°C at the feed throat to 195°C at the die plate; oil is injected downstream of the melt seal to avoid feed-zone slip and screw seizure. Extruded pellets are subsequently processed on a 20–24:1 L/D single-screw medical extruder fitted with a crosshead tubing die, with draw-down ratio maintained between 1.5:1 and 3:1 to control lumen concentricity and prevent melt fracture at the tube surface. Biocompatibility is assessed under ISO 10993-1:2018, with USP Class VI extraction testing and food-contact compliance verified against FDA 21 CFR 177.1810 and EU 10/2011. Terminal components include IV administration set tubing, peristaltic pump segments, enteral feeding tubes, respiratory mask cushions, and disposable bag ports. Steam autoclaving above 121°C is not recommended unless the compound has been specifically stabilized for repeated sterilization, and aromatic mineral oils are excluded because extractable UV-absorbing fractions can exceed medical-device limits.
| Standard | Scope | Endpoint |
|---|---|---|
| ISO 10993-1:2018 | biological evaluation of medical devices | cytotoxicity, sensitisation, irritation |
| USP Class VI | extraction and acute systemic injection | plastics and containers |
| FDA 21 CFR 177.1810 | styrene block polymers | food-contact use conditions |
| EU 10/2011 | plastic materials in food contact | overall migration and specific migration limits |
Impact modification of clarified random copolymer polypropylene with 5–15 wt% G1730 addresses low-temperature brittleness at −20°C while retaining contact clarity in thin-wall articles. The addition ratio is kept below 15 wt% because the styrenic block copolymer forms a dispersed rubber phase with a refractive index close to the clarified PP matrix; above this threshold, coarsened rubber particles reduce flexural modulus below 900 MPa and raise haze beyond acceptable limits for transparent food-service articles. Processing is carried out either by direct pellet-to-pellet dosing at the injection molding hopper with melt homogenization at 190–230°C, or by pre-compounding on a 36:1 L/D twin-screw extruder before pelletizing. Mold temperatures between 10°C and 30°C are used to minimize haze and shorten cycle time, but the mold must be vented to avoid splay caused by moisture in the PP carrier. Compliance for food-contact uses is evaluated under FDA 21 CFR 177.1810 and EU 10/2011, with the final article tested for overall migration in 10% ethanol and 3% acetic acid. Terminal products include clear deli containers, thin-wall cups, snack packaging lids, and refrigerator storage boxes. The formulation is unsuitable for hot-fill above 90°C and should not be combined with high-melt-flow PP grades that require processing temperatures above 240°C, because thermal degradation of the styrenic endblock reduces impact strength and promotes yellowing.
Because G1730 imparts cohesive strength without the high melt viscosity of higher-molecular-weight SEBS grades, hot-melt pressure-sensitive adhesives are formulated with 10–25 wt% polymer, 40–60 wt% hydrogenated C5 tackifier, and 15–25 wt% paraffinic oil. The addition ratio is set by the required loop tack and shear holding power; higher G1730 content increases cohesive strength but reduces wet-out, while higher oil content lowers plateau modulus and can cause adhesive transfer to the release liner. Adhesive production uses a jacketed sigma-blade mixer or a 20–30:1 L/D twin-screw extruder at 150–180°C under nitrogen blanketing; the molten adhesive is slot-die coated onto release liner at 150–170°C with coat weights between 20 g/m² and 40 g/m². Viscosity is measured by ASTM D3236, loop tack by ASTM D6195, and 180° peel by ASTM D3330. For food-service label stocks, the adhesive must comply with FDA 21 CFR 175.105; for medical tapes, the coated article is evaluated under ISO 10993-1. Terminal products include clear label stocks, medical fixation tapes, protective film adhesives, and assembly tapes. Continuous operating temperature is limited to 70°C; above this threshold shear holding time drops steeply, and the adhesive should not be specified for bonding low-surface-energy substrates without corona treatment or a primer.
G1730 is added at 5–12 wt% to naphthenic or paraffinic process oil in low-viscosity gel applications where the fully hydrogenated midblock imparts gel structure without excessive melt viscosity. The addition ratio is controlled within this band because below 5 wt% the gel exhibits oil exudation and fails cone penetration stability, while above 12 wt% the high-shear mixing temperature rises and the cooled gel becomes too firm for pumping into cable interstices. Dispersion is carried out in a heated high-shear disperser or stirred tank at 125–150°C, followed by vacuum deaeration at −0.09 MPa and cooling under low shear to prevent premature gel fracture. Cone penetration is measured according to ASTM D217, with typical target values between 200 dmm and 300 dmm adjusted by oil aromaticity and polymer loading; oxidative stability is evaluated by ASTM D942. The final filling compound must comply with RoHS 2011/65/EU, and halogen-free integrity is verified by IEC 61249-2-21. Terminal applications include fiber optic buffer tubes, water-blocking cable fillers, electrical joint encapsulation gels, and vibration-damping gel pads. The compound is not suitable for continuous service above 80°C, and aggressive high-shear pumping after gel formation should be avoided because the physical network is not fully thermally reversible over repeated shear cycles.
Soft-touch overmoulding compounds based on G1730 at 30–60 wt%, combined with 20–40 phr white mineral oil and 10–25 phr polypropylene, are used where the finished overmould must exhibit a Shore A hardness of 52–58 A and fill ribs as thin as 0.8 mm. The low-viscosity profile of G1730 reduces injection pressure at the second-shot gate, but the processing window must be constrained to 190–220°C barrel temperature and 20–40°C mold temperature to prevent gate freeze before the cavity is packed. Two-shot injection molding with a rotating platen or core-back mold is used; the substrate surface temperature is maintained above 60°C to improve interfacial interdiffusion. Adhesion to polypropylene substrates is achievable without a primer, while PC/ABS and nylon substrates require a maleic anhydride-grafted SEBS tie layer because neat G1730 does not form chemical bonds to polar engineering thermoplastics. Hardness is verified to ASTM D2240, tensile properties to ISO 37:2017, and abrasion resistance to ASTM D4060. REACH and RoHS 2011/65/EU compliance is confirmed by supplier declaration and targeted migration screening. Terminal parts include power tool grips, personal care appliance handles, consumer electronics housing overmoulds, and protective corners. Continuous service above 80°C is not recommended for the overmoulded layer, and direct contact with strong solvents, especially ketones and esters, must be excluded.
For rotary and compression closure systems, G1730 is compounded at 20–60 wt% with 20–45 phr mineral oil and 10–25 phr polypropylene to produce cap liners and jar-sealing rings with a Shore A hardness between 45 A and 65 A. The processing route is injection molding or compression molding at melt temperatures between 180°C and 200°C, with mold temperatures held at 15–30°C to reduce seal surface tack and improve part release. The formulation is used only for low-to-intermediate fat food matrices because high oil content in the packaged product can extract process oil from the liner and increase organoleptic risk. Compliance is verified under FDA 21 CFR 177.1810 and EU 10/2011, with overall migration tested in aqueous and alcoholic simulants; the final closure must meet seal integrity parameters established by the packaging converter. Terminal parts include beverage cap liners, jar sealing rings, PET closure gaskets, and induction-seal wads. The compound is unsuitable for hot-fill above 80°C and for retort packaging, and it must not be combined with unsaturated process oils that reduce oxidative stability and cause odor development.
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Kraton™ G1730 is a linear triblock copolymer of styrene and ethylene/butylene (SEBS) supplied as dusted dense pellets. Typical neat-polymer data place bound styrene between 21 wt% and 23 wt%, density at 0.90–0.92 g/cm³ when measured per ISO 1183-1, and melt mass-flow rate at 1.0–3.0 g/10 min under a 230 °C/5 kg piston load per ISO 1133-1:2022. The saturated ethylene/butylene mid-block removes the main-chain unsaturation present in styrene-butadiene-styrene grades, which changes oxidative stability, melt rheology, and low-temperature torsional damping. These values define the uncompounded polymer before oil extension or filler addition; exact lot values are governed by the supplier certificate of analysis, and commercial compounds should not be designed against these values alone.
Compared with higher-styrene SEBS grades such as Kraton G1652 and Kraton G1654, both of which carry styrene mass fractions near 30 wt%, G1730 is positioned at a lower aromatic styrene fraction. The reduction to approximately 22 wt% lowers room-temperature tensile modulus and Shore hardness while increasing elongation. This distinction becomes measurable in oil-extended formulations, where a 50 phr white paraffinic oil addition commonly produces a hardness of 25–35 Shore A, depending on filler and polypropylene content. Hardness response should be confirmed by ASTM D2240-15e1 on compression-molded plaques conditioned at 23 °C/50% RH for 24 h. The lower styrene content also reduces die swell in profiles and improves clarity in thin films, but it reduces the cohesive strength of the styrenic end-block network.
The saturated mid-block provides lower susceptibility to chain scission during melt processing and service than unsaturated butadiene-containing SBS grades. Thermogravimetric analysis under nitrogen at 20 K/min typically shows onset mass loss near 380–400 °C; in air, oxidative mass loss accelerates above 200 °C. Processing above 260 °C should therefore be limited to short residence times below 5 min to avoid yellowing and molecular-weight loss. The saturated structure also improves retention of elongation after oven aging at 100 °C for 168 h, but long-term ultraviolet exposure still requires stabilizer loading. Primary antioxidant addition is typically 0.1–0.3 wt% of a hindered phenolic, with secondary phosphite at 0.1–0.2 wt%. Total antioxidant loading above 0.5 wt% can plate out on die lips and reduce clarity. Published data for G1730-specific outdoor weathering per ISO 4892-2 are limited; compounders should generate lot-specific data when exterior service is required.
Compounding of Kraton™ G1730 on a corotating twin-screw extruder with an L/D ratio of 40:1 is performed at a screw speed of 300–500 min⁻¹. The barrel profile from feed to die is typically 180 °C, 190 °C, 200 °C, 210 °C, 220 °C, 220 °C, 230 °C, with melt temperature held below 250 °C at the die plate. White paraffinic oil is injected at barrel 4–6 downstream from the feed throat to allow complete fusion of the neat SEBS before oil wetting; early oil injection at barrel 2 can cause screw slippage, torque instability, and elevated melt-pressure fluctuation. Side-stuffing of calcium carbonate beyond 20 wt% increases specific energy input by approximately 10–20% and requires atmospheric or vacuum venting to remove residual moisture. A vacuum level of −0.06 MPa to −0.08 MPa at the final vent reduces volatiles to below 0.1 wt% in pelletized compound.
Pre-drying is required only when surface moisture exceeds 0.05 wt%; pellet trays should be dried at 70–80 °C for 2–3 h with air dew point below −20 °C. Avoid combination of the polymer with amine-based antistats in peroxide-containing formulations because residual amines interfere with radical crosslinking and accelerate discoloration. Strong oxidizing acids and chlorinated solvents at elevated temperature are also incompatible with the ethylene/butylene mid-block and should not be used in cleaning or dilution systems.
Specific mechanical values for the neat polymer are not uniformly reported because SEBS is rarely sold as a finished article; tensile data are generated on compression-molded sheets after conditioning. Representative reported neat-film tensile strength ranges from 15 MPa to 25 MPa with elongation at break above 700% when tested per ASTM D412-16. Oil extension reduces tensile strength and modulus but increases elongation in proportion to the added paraffinic oil. A formulation with 50 phr white oil and no filler typically exhibits tensile strength of 3–8 MPa and elongation above 800%. Compression set values measured by ASTM D395-18 at 70 °C/22 h generally fall between 40% and 80%, depending on oil level, filler, and crosslinking additives. These ranges are illustrative; commercial compounds must be validated against application-specific specifications.
| Property | Test method | Typical neat polymer value |
|---|---|---|
| Bound styrene | Internal FTIR / ¹H NMR | 21–23 wt% |
| Density | ISO 1183-1 | 0.90–0.92 g/cm³ |
| Melt mass-flow rate | ISO 1133-1:2022 at 230 °C/5 kg | 1.0–3.0 g/10 min |
| Volatile matter | ASTM D5668 | <0.5 wt% |
| Ash | ISO 3451-1 | <1.0 wt% |
For injection-molded soft-touch grips and diaphragm components, a screw with L/D 20:1–24:1 and compression ratio 2.5:1–3.0:1 is used. Barrel zones are set at 180 °C, 200 °C, 210 °C, 220 °C, nozzle 220 °C, and mold cooling water at 20–40 °C. Holding pressure of 30–50 MPa and back pressure of 0.5–1.5 MPa control sink marks and gate blush. Clamp force requirements scale from 800 kN for thin-wall closures to 2,500 kN for multicavity medical housings. Shot sizes should use 60–80% of barrel capacity to limit residence-time variability.
In medical device applications where extraction resistance and sterilization tolerance are evaluated, the saturated mid-block of G1730 reduces the concentration of oxidizable allylic hydrogen sites relative to butadiene-containing SBS. This does not eliminate the need for extraction testing under ISO 10993-12:2021 or hemocompatibility testing under ISO 10993-4:2017. Gamma irradiation at 25–50 kGy may induce crosslinking and a measurable increase in Shore A hardness of 2–5 points; ethylene oxide sterilization is generally less aggressive to SEBS but requires residuals testing per ISO 10993-7:2008. The polymer has been referenced in food-contact evaluations under FDA 21 CFR 177.1810 and in EU plastics migration testing under Regulation (EC) No 10/2011, but final formulation compliance depends on additives, fillers, colorants, and processing aids. Devices marketed with a medical claim require supplier drug master file or regulatory dossier support; the neat polymer alone does not confer device approval.
Hot-melt adhesive formulations based on G1730 use hydrocarbon tackifier addition of 40–60 wt% and a processing temperature of 180–200 °C in sigma-blade or agitated batch mixers. Open time and loop tack are controlled by Brookfield viscosity at 180 °C. In polypropylene impact modification, loading at 5–15 wt% reduces notched Charpy impact transition temperature when measured per ISO 179-1:2020; the exact improvement depends on matrix melt-flow rate and compatibilizer level. Published data for G1730 in co-continuous PP/SEBS systems with filler loadings above 30 wt% are limited, and application-specific compounding trials are required.