| HS Code | 540511 |
| Productname | Kraton Kraton™G SEBS G1641 HU |
| Polymertype | SEBS |
| Structure | Linear triblock copolymer |
| Midblock | Ethylene/butylene |
| Hydrogenation | Hydrogenated |
| Styrenecontent | 32% |
| Form | Powder |
| Specificgravity | 0.91 |
| Shoreahardness | 42 |
| Tensilestrength | 27.6 MPa |
| Elongationatbreak | 500% |
| 300 Modulus | 4.8 MPa |
| Tearstrength | 35 kN/m |
| Bulkdensity | 0.4 g/cm3 |
| Volatilematter | <0.5% |
As an accredited Kraton Kraton™G SEBS G1641 HU factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ G SEBS G1641 HU is supplied in 25 kg net paper bags, typically palletized at 1,000 kg per pallet. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Kraton™G SEBS G1641 HU palletized, shrink-wrapped, and securely braced for safe ocean transport. |
| Shipping | Kraton™ G SEBS G1641 HU is shipped as non-hazardous polymer pellets in 25 kg bags or 1,000 kg super sacks. It is not regulated as dangerous goods for transport; no UN number, hazard class, or packing group applies. Store and ship dry at ambient temperature, avoiding moisture, heat, and direct sunlight. |
| Storage | Store Kraton™ G SEBS G1641 HU in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep containers tightly closed in original packaging and protect contents from moisture, dust, and contamination. Avoid contact with strong oxidizing agents. Practice good housekeeping and use secondary containment where appropriate to control spills. |
| Shelf Life | Kraton™G SEBS G1641 HU has a shelf life of 2 years from date of manufacture when stored unopened in original packaging under dry, ambient conditions. |
Compounding Kraton™ G1641 HU into a soft-touch automotive interior grade requires limiting both the shear-induced temperature rise and the residence-time distribution in the twin-screw extruder. The linear triblock structure of G1641 HU, with a styrene endblock weight fraction in the 32–34 wt% range, produces thermolabile physical crosslinks that are disrupted in barrel zones 5–9 where melt temperatures are maintained between 190°C and 230°C. On production-scale 40:1 L/D co-rotating twin-screw extruders with screw diameter 50–75 mm, screw configurations with two or three neutral kneading blocks downstream of the oil injection port achieve acceptable dispersion without over-shearing the elastomer network. A formulation for injection-molded door panel inserts contains 25–40 wt% G1641 HU, 15–30 wt% polypropylene homopolymer with a melt flow rate of 20–35 g/10 min under ISO 1133-1:2022 at 230°C/2.16 kg, 20–35 wt% hydrogenated white mineral oil, and 0–15 wt% calcium carbonate or talc. The compounding rate is constrained by the oil absorption capacity of the undusted pellet; screw speeds above 600 rpm on a 60 mm line can induce frictional hotspots that degrade the ethylene-butylene midblock and raise volatile organic compound emissions. The pelletized compound is dried at 80°C for 2–3 hours when storage relative humidity exceeds 60% before injection molding. Injection molding is performed at barrel 200–230°C, mold 30–50°C, injection pressure 60–90 MPa, and clamp force selected to avoid flash without excessive packing stress. Regulatory compliance is anchored to RoHS Directive 2011/65/EU, REACH Regulation 1907/2006, thermal desorption testing under VDA 278:2011, and fogging testing under ISO 6452:2007. Individual OEM specifications commonly require VOC values below 100 µg/g and FOG values below 250 µg/g. Terminal product types include door panel inserts, center console armrest skins, glove box soft-touch laminas, lower instrument panel trim, and HVAC control knob inserts.
Hot-melt pressure-sensitive adhesive compounding with Kraton™ G1641 HU is done in a heated sigma-blade or planetary mixer under nitrogen blanketing at 0.3–0.5 MPa positive pressure to prevent midblock oxidation. The polymer is charged first and masticated for 5–10 minutes until the torque curve stabilizes; a hydrogenated hydrocarbon tackifier with ring-and-ball softening point 95–110°C under ASTM E28-18 is then added incrementally, followed by naphthenic oil. The addition window for G1641 HU is 15–30 wt%, with tackifier at 40–60 wt%, oil at 15–25 wt%, and hindered phenolic antioxidant at 0.5–1.0 wt%. Below 15 wt% polymer loading, cohesive strength and high-temperature shear resistance fall below acceptable industrial thresholds; above 30 wt%, mixer torque can exceed the capability of production-scale 500 L sigma-blade units and the adhesive becomes difficult to coat through a slot die at 150–170°C. The compounded adhesive is pumped through melt filtration with 100 µm screen packs and coated onto 25–36 µm polyester film or nonwoven carrier at coating weight 18–25 g/m². For food packaging label applications, the finished adhesive is evaluated under FDA 21 CFR 175.125 and, where the adhesive forms part of a food-contact article, under FDA 21 CFR 177.1810. Adhesive performance is measured using PSTC-16 loop tack, ASTM D3330/D3330M-23 for 180° peel on stainless steel, and ASTM D3654/D3654M-22 for static shear holding at 70°C with 500 g load. Terminal product types include high-cohesion assembly tapes, label stocks for chilled-food cartons, hygiene positioning adhesives, and temporary protective films for appliance panels.
At asphalt processing temperatures above 180°C, the high molecular weight linear triblock of Kraton™ G1641 HU requires a pre-dispersion step through a rotor-stator high-shear mixer before addition to a bituminous base. In torch-applied and self-adhered waterproofing membrane plants, SEBS modification is not a simple melt blending operation: the saturated midblock of G1641 HU is less sensitive to oxidative chain scission than SBS, but its high solution viscosity can produce elastomeric domains that remain as discrete gels unless the mixing energy input exceeds the threshold for cohesive disruption. The polymer loading is typically 6–12 wt% of the total compound, with penetration-grade bitumen at 50–65 wt%, maltene-compatible or naphthenic extender oil at 0–8 wt%, and mineral filler or stabiliser at 0–30 wt% depending on the target bending temperature. The process sequence uses a high-shear rotor-stator mixer operating at 2,500–4,000 rpm for 30–60 minutes at 180–200°C, followed by a low-shear paddle mixer at 170–180°C to avoid excessive viscosity rise. If the blend temperature exceeds 200°C, oil volatilisation and oxidative hardening increase the softening point beyond the application window, while insufficient shear leaves polymer-rich islands that cause low-temperature flex failure. The mixed membrane compound is coated onto polyester or glass-fibre reinforcement and surfaced with mineral granules or polymeric film in accordance with ASTM D5147/D5147M-18 and EN 13707:2004+A1:2008. Rotational viscosity is monitored by ASTM D4402/D4402M-23 at 180°C with a Brookfield Thermosel. Published plant-scale data for G1641 HU in oxidised bitumen configurations is limited, so low-temperature flex screening under ASTM D5147 remains mandatory for each formulation change. Terminal product types include torch-applied modified bitumen membranes, self-adhered roofing underlayment, bridge deck waterproofing sheets, and plaza deck vapour barrier courses.
Oil-bleed resistance in SEBS medical tubing is controlled less by total oil loading than by the aromaticity of the plasticizer and the endblock glass transition of the styrene domains. Kraton™ G1641 HU is selected for short-term body-contact devices where undusted pellets reduce silicone and silica contamination in cleanroom compounding; the polymer is formulated at 35–55 wt% with 10–20 wt% medical-grade polypropylene random copolymer, 25–45 wt% USP-grade white mineral oil, and 0.05–0.2 wt% of a phenolic/phosphite stabiliser system. The compounding operation uses a 40:1 L/D co-rotating twin-screw extruder with all product-contact surfaces in 316L stainless steel, double vacuum venting at -0.08 MPa, and melt filtration through 100 µm sintered mesh to capture char particles. Barrel temperatures are maintained at 180–220°C, with the oil injection port located after the first kneading section to prevent viscosity reduction before the polymer melts. The resulting compound is extruded into tubing with outside diameter 2–10 mm at line speeds 20–80 m/min, using a single-screw extruder with L/D 25:1, a crosshead die, and water cooling at 15–25°C. Medical toxicity assessment is performed under ISO 10993-5:2009 for cytotoxicity and ISO 10993-10:2021 for irritation and skin sensitisation; USP <87> and USP <88> Class VI protocols are commonly requested for materials used in fluid-contact components. The formulation boundary is defined by oil bleeding: loading above 45 wt% white mineral oil can produce surface exudation after ethylene oxide sterilization at 55°C, especially when compounded with low molecular weight oils. Amine-based heat stabilizers are excluded because they can form coloured by-products during gamma irradiation at 25–40 kGy. Published dose-response data for G1641 HU-specific gamma irradiation is limited, so radiation validation at the upper dose limit is required for each tubing geometry. Terminal product types include enteral feeding extension sets, respiratory circuit components, peristaltic pump tubing, IV drip chamber bodies, and syringe gaskets.
Phthalate-free soft toy compounds that pass EN 71-3:2019+A1:2021 migration limits require a balance between low oil leachability and Shore A 30–50 softness. Kraton™ G1641 HU is formulated at 30–45 wt% with 35–55 wt% medical white mineral oil, 10–20 wt% polypropylene homopolymer, and 0–3 wt% fumed silica for surface dryness. The fumed silica addition is the controlling variable for teething ring surfaces: below 0.5 wt%, injection-moulded parts can show tacky surface transfer to packaging; above 3 wt%, Shore A hardness climbs beyond the toddler mouth-feel window and the compound becomes difficult to overmould onto polypropylene inserts. The formulation is pre-compounded on a 40:1 L/D twin-screw extruder at 180–220°C, then injection moulded at 190–230°C with mold temperature 20–40°C. Overmoulding onto a 20–30 wt% mineral-filled polypropylene substrate is carried out in a two-shot press or by insert moulding; the substrate surface is maintained above 60°C at the point of elastomer introduction to prevent premature solidification and delamination. Hardness is checked under ASTM D2240-15(2021) after 24 hours conditioning at 23±2°C and 50±5% relative humidity. Regulatory compliance is documented under EN 71-3:2019+A1:2021 for migration of 19 elements, ASTM F963-23 for U.S. toy safety, REACH Annex XVII entries 51 and 52 for phthalates, and CPSIA Section 108. Terminal product types include squeeze toys, teething rings, pacifier handles, bath toy films, and soft overmoulded grips on infant training cups.
Before jacket extrusion begins, a 2.0 mm pressed plaque is conditioned for 24 hours at 23±2°C and 50±5% relative humidity before tensile bars are stamped for ASTM D638-14 Type 4 testing. Kraton™ G1641 HU is used in halogen-free jacket compounds at 25–50 wt%, combined with 10–20 wt% polyolefin elastomer, 20–40 wt% magnesium dihydroxide or alumina trihydrate, 5–15 wt% paraffinic oil, and 0.2–0.5 wt% antioxidant. The production line employs a 70 mm Buss co-kneader or a 58 mm co-rotating twin-screw extruder with a temperature profile of 170–200°C for dispersion of the flame-retardant filler, followed by an extrusion jacket line with L/D 25:1, crosshead die, and melt temperature set at 190–210°C. The key processing conflict is flame-retardant filler loading against tensile elongation: when filler exceeds 40 wt%, elongation retention after 7 days at 100°C can drop below the 125% minimum specified in halogen-free cable standards, while filler below 20 wt% may fail the IEC 60332-1-2:2015 single-wire flame propagation test. The jacket compound is evaluated under IEC 62821-1:2015 for halogen-free thermoplastic insulated and sheathed cables and under IEC 60811-401:2012 for thermal ageing methods; dimensional stability is checked by the hot-pressure test at 70°C. Where North American flexible cord listing is required, UL 62:2018 may also apply to the finished cord assembly. Terminal product types include electric vehicle charging cable jackets, robotic flex-cable sheaths, appliance power cords, data centre power distribution cords, and signal cable jackets for sound systems.
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Kraton Kraton™ G SEBS G1641 HU is a linear hydrogenated styrene-ethylene/butylene-styrene block copolymer supplied as dusted pellets for compounding with polyolefins and hydrocarbon oils. The polymer has a typical styrene content of 30 wt% and a neat specific gravity of 0.91 g/cm³ when characterized under ASTM D792. Because the midblock is saturated, thermo-oxidative stability is higher than that of unhydrogenated styrene-butadiene-styrene block copolymers, but the grade still requires antioxidant stabilization in most melt operations. The material is used where low compression set, soft-touch haptics, and adhesion to polypropylene are required; application examples include automotive interior skins, appliance grip compounds, and medical device components subject to regulatory verification. Published single-point mechanical data for the neat block copolymer are limited, and most design data are generated on oil/PP compounds based on target Shore A hardness rather than on the unmixed block copolymer.
Drying of the dusted pellets before melt mixing is recommended when storage humidity exceeds 60% RH. A desiccant dryer with inlet air dew point of -40°C at 70–80°C for 2–4 h reduces surface moisture to below 0.1 wt%; higher moisture contributes to splay in injection-molded parts and increases the risk of surface defects at melt temperatures above 200°C. Compounding on a co-rotating twin-screw extruder with L/D ratio between 32:1 and 40:1 and modular screw elements permits dispersion of the high-molecular-weight rubber phase. Barrel settings from 170°C to 210°C, die temperature 210–220°C, and melt temperatures not exceeding 230°C are typical; residence times beyond 8 min at 230°C risk viscosity shifts from midblock chain scission. The melt exhibits pronounced shear thinning; characterization by capillary rheometry per ISO 11443 at 230°C provides apparent viscosity curves for mold-fill simulation, while instrumented injection molding with cavity pressure sensors helps define the narrow hold-pressure window when thin-wall regrind is used. For injection molding, melt temperatures of 190–220°C, mold temperatures of 20–40°C, and holding pressures of 40–60 MPa are usual starting points for PP-based compounds; higher mold temperatures improve flow mark elimination but extend cooling time.
Where automotive interior soft-touch compounds are specified, G1641 HU is typically co-continuous with polypropylene at addition levels above 40 wt%. Oil absorption into the ethylene/butylene midblock lowers hardness and improves processability, but oil loadings above 80 phr can reduce mar resistance and increase migration under the conditions of DIN 75201-A fogging. Formulators often screen compounds by VDA 278 for VOC and FOG values because OEM specifications impose ceilings on condensable emissions; results depend on oil type, additive package, and melt compounding temperature. Adhesion to PP substrates is generally sufficient when the substrate surface temperature during overmolding reaches at least 120°C and the molded compound contains no excessive release agent. A production-scale twin-screw extruder with side feeder and vacuum venting at -0.08 MPa is used to devolatilize low-molecular-weight process aids; observed delamination in two-component parts is often traceable to insufficient melt temperature at the interface rather than incompatibility of the SEBS phase.
The principal structural distinction is saturation of the midblock. Unhydrogenated SBS contains double bonds that are vulnerable to ozone, UV, and thermal oxidation; G1641 HU has an ethylene/butylene midblock that raises upper use temperature and UV resistance but lowers the tear propagation resistance and solvent affinity of the diene block. Within SEBS grades, the 30 wt% polystyrene content of G1641 HU produces higher room-temperature stiffness and tensile strength than grades at 13 wt% or 20 wt% styrene, but reduces low-temperature flexibility and requires more heat to disrupt the styrene domains. The HU designation corresponds to a supplied stabilization package intended for applications with strong UV exposure; however, no outdoor weathering claim should be based on the block copolymer alone because expressed service life depends on pigment, UV absorber, and part thickness. Property comparisons must be made after the same formulation and mixing history because neat SEBS tensile properties are rarely used for final part design. Tensile properties after compression molding are typically reported under ASTM D412, hardness under ASTM D2240, and compression set under ASTM D395 method B at 70°C or 100°C.
When food-contact, medical, or automotive emission testing is invoked, the exact compound formulation rather than the base polymer controls most compliance outcomes. Kraton™ G1641 HU belongs to the styrene block copolymer class that is referenced in FDA 21 CFR 177.1810 for certain food-contact articles; current supplier regulatory certificates and extraction data should be checked because the base polymer alone is not an article. For medical devices, ISO 10993-5 cytotoxicity and ISO 10993-10 skin sensitization are performed on the final sterilized part; the polymer is not autoclave-stable in all filled or oil-modified compounds, and gamma resistance should be verified at the highest intended dose. Automotive interior compounds may be tested under VDA 278 for VOC and fogging, VDA 270 for odor, and DIN 75201-A for gravimetric fogging. RoHS 2011/65/EU screening and REACH SVHC candidate-list confirmation are mandatory for electrical and electronic equipment components but apply to the compound as supplied.
| ASTM D1238 | Melt flow index, 230°C / 5.0 kg |
| ASTM D792 | Specific gravity of neat polymer |
| ASTM D2240 | Shore hardness after compounding |
| ASTM D412 | Tensile strength and elongation at break |
| ASTM D395 method B | Compression set at 70°C and 100°C |
| FDA 21 CFR 177.1810 | Food-contact article clearance for styrene block copolymers |
| EU Regulation 10/2011 | Overall migration limit 10 mg/dm² |
| RoHS 2011/65/EU | Restricted substance screening |
In oil-extended PP compounds, the effective SEBS volume fraction determines whether the styrene-rich phase acts as a continuous physical network. At G1641 HU additions between 30 wt% and 50 wt%, phase morphology often transitions from PP continuous to co-continuous; oil selectively swells the ethylene/butylene block and reduces melt viscosity, but excessive oil addition can suppress the reinforcement of the styrene domains and increase compression set. Mixing on a twin-screw extruder with side-fed oil at the second barrel and downstream PP addition produces a finer morphology than single-pass preblends, as evaluated by scanning electron microscopy after selective extraction of the rubber phase. The styrene blocks form glassy domains that associate below approximately 100°C; the compound therefore exhibits solid-state physical crosslinks without sulfur or peroxide cure. This reversible network contributes to the compression set behavior measured under ASTM D395 method B, but the network softens above the glass transition of styrene, which limits the upper service temperature compared with TPV grades containing chemical crosslinks. Publicly available compounding guidance for 60–65 Shore A soft-touch compounds often indicates starting formulations containing 30–40 wt% G1641 HU, 10–20 wt% polypropylene homopolymer with MFR of 20 g/10 min at 230°C/2.16 kg, and 30–40 wt% paraffinic oil. The mixture is preblended in a low-speed ribbon blender and extruded with side-fed oil; hardness is measured after 24 h at 23°C and 50% RH according to ASTM D2240. Increasing oil to 50 wt% can lower Shore A by 15–20 points but raises compression set and fogging potential. Tensile strengths under ASTM D412 typically range from 5 MPa to 12 MPa for such compounds, with elongation at break above 400%. These values are strongly influenced by the choice of polypropylene and oil and do not represent properties of the neat block copolymer.
Operational limitations include irreversible hardening after prolonged exposure to aromatic oils or ester plasticizers due to styrene domain plasticization, and swelling in ketone or aromatic hydrocarbon solvents. The grade should not be processed in equipment previously contaminated with amine-based stabilizers used for diene rubbers if surface bloom is a concern. Storage in closed original packaging at temperatures below 30°C and away from UV minimizes lot-to-lot variation; when block copolymer powder dusting is acceptable for the compounding process, the dusted pellet form can be used as supplied without additional external lubricants. Published data for thin film or fiber extrusion configurations using the neat HU grade are limited, and end-user validation on production-scale equipment is required before changing from a lower-molecular-weight SEBS or an unhydrogenated SBS.