| HS Code | 863213 |
| Productname | Kraton Kraton™G SEBS G1652 M |
| Polymertype | Linear styrene-ethylene-butylene-styrene (SEBS) triblock copolymer |
| Styrenecontent | 30% by weight (typical) |
| Diblockcontent | <1% by weight |
| Physicalform | Powder |
| Specificgravity | 0.91 |
| Density | 0.91 g/cm³ |
| Meltflowrate | 5 g/10 min at 230°C/5 kg |
| Hardnessshorea | 65 |
| Tensilestrength | 35 MPa |
| Elongationatbreak | 500% |
| 300percentmodulus | 4.5 MPa |
| Vicatsofteningpoint | 65°C |
| Glasstransitiontemperature | -55°C |
| Bulkdensity | 0.4 g/cm³ |
| Volatilematter | <1% |
| Ashcontent | <1% |
As an accredited Kraton Kraton™G SEBS G1652 M factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ G SEBS G1652 M comes in 25 kg moisture-barrier paper bags, typically palletized for bulk industrial use. |
| Container Loading (20′ FCL) | Loaded in a 20-foot FCL container, Kraton™ G SEBS G1652 M is packed in standard bags on pallets, secured for ocean transport. |
| Shipping | Kraton™ G SEBS G1652 M is a non-hazardous thermoplastic elastomer supplied as pellets. Ship in dry, closed bags or boxes at ambient temperature, protected from moisture, heat, and sunlight. Not classified as dangerous goods; no UN number or special transport label required. |
| Storage | Store Kraton G1652 M in a cool, dry, well-ventilated area, preferably in the original sealed packaging. Protect from direct sunlight, moisture, heat, and ignition sources. Keep containers closed to prevent contamination and dust accumulation. Store away from strong oxidizing agents and incompatible chemicals. Follow local regulations and manufacturer’s shelf-life guidance. Ensure good housekeeping and avoid excessive stacking. |
| Shelf Life | Stable for 24 months from manufacture when stored in original sealed packaging under cool, dry, normal conditions. |
Interior soft-touch compounds based on Kraton G1652 M, a linear triblock with a styrene content of 30 wt%, are processed on high-torque co-rotating twin-screw extruders with L/D 44:1 for automotive interior applications. Compliance requirements for serial-production instrument panel or door panel insert materials derive from REACH Regulation (EC) No 1907/2006, RoHS Directive 2011/65/EU, ELV Directive 2000/53/EC, and IATF 16949:2016; emissions are characterized by VDA 278 for VOC and FOG, with commonly targeted limits of ≤100 µg/g for VOC and ≤250 µg/g for FOG depending on OEM specification, and VDA 270 odor below grade 3.0. Formulation addition ratios in a 45–75 Shore A interior TPE compound typically load G1652 M at 25–40 wt%, polypropylene at 15–25 wt%, hydrotreated white oil at 30–45 wt%, primary phenolic antioxidant at 0.1–0.3 phr, secondary phosphite process stabilizer at 0.1–0.3 phr, and hindered amine light stabilizer at 0.2–0.5 phr. The compounding sequence is critical: polymer and PP are gravity-fed into the main throat, a first intensive kneading section melts the polymers at 170–200 °C, oil is injected through side liquid ports in 2–3 aliquots after the melt seal has formed, and downstream vacuum devolatilization at -0.08 MPa removes low-volatility oil fractions. Barrel temperatures from main throat to die are maintained between 180 °C and 230 °C; melt temperatures above 250 °C produce a measurable shift in ISO 1133-1 melt flow rate and yellowing, while die-head pressure above 25 MPa indicates overfilled kneading sections or insufficient oil incorporation. On production extruders, torque spikes at the initial oil injection port occur when oil is dosed at more than 5 wt% per injection zone; the practical remedy is to split oil injection across at least 2 ports and raise the second kneading zone temperature by 5–10 °C. After underwater pelletizing and drying to residual moisture below 0.1 wt%, the compound is injection-molded at melt temperatures of 190–220 °C, mold temperatures of 30–50 °C, holding pressures of 40–60 MPa, and back pressure of 5–10 MPa. Optical and tactile surfaces require vent depth below 0.02 mm and purge shots after each color change. Critical failure modes on production lines are surface oil bloom after 7 days at 70 °C in ISO 188 heat aging, gloss reduction from improper mold temperature, and knife-line adhesion loss at gate locations. Published data for this specific grade in serial OEM interior approvals is limited, so final compound validation remains the responsibility of the compounder. Terminal finished product types include instrument panel soft skins, door panel inserts, HVAC seal profiles, gear shift boots, and floor mat edges.
In cleanroom medical-device compounding, a linear triblock containing 30 wt% styrene is used as the major elastomer for flexible components where final-article biocompatibility is the gate criterion. Compliance obligations are covered by ISO 10993-5 for in vitro cytotoxicity, ISO 10993-10 for sensitization and irritation, USP <87> and USP <88> for biological reactivity in Class VI testing, ISO 13485:2016 for the device compounder’s quality management, and FDA 21 CFR 177.1810 for styrene block polymers intended for food-contact articles where applicable; if the article is used in European food-contact contexts, overall migration is assessed under EU 10/2011/EC with an overall migration limit of 10 mg/dm². Formulation addition ratios for a flexible medical tubing compound place G1652 M at 50–70 wt%, clarified polypropylene at 5–15 wt%, high-purity white mineral oil at 20–30 wt%, a radiopacifier such as barium sulfate at 10–20 wt%, and a low-phenolic antioxidant at 0.1–0.3 phr. Production compounding is performed on a 40:1 L/D co-rotating twin-screw extruder with vacuum devolatilization at -0.08 MPa and melt temperature limited to 180–210 °C; barrel zone temperatures are kept below 210 °C because thermal decomposition by-products elevate extractables and can shift ISO 10993-5 cytotoxicity scores. Compounded pellets are pre-dried at 80 °C for 2 h whenever warehouse relative humidity exceeds 60%, then tubular profiles are extruded through a 24:1 L/D single-screw extruder with melt temperature 190–205 °C, die temperature 200 °C, and cooling water at 15–25 °C. Wall thickness control is maintained at ±0.02 mm through closed-loop gauge control. Gamma sterilization at 25–40 kGy is commonly applied to terminal devices; published data for this specific grade above 50 kGy is limited, and post-sterilization tensile retention per ISO 37 must be verified on the finished compound rather than assumed from resin data. Terminal finished product types include IV administration set tubing, syringe plunger tips, peristaltic pump tubing, blood collection tube closures, and medical films for device pouches.
Where hot-melt assembly and pressure-sensitive adhesives must survive carton or automotive-interior service temperatures, the styrenic endblock network in G1652 M is the dominant cohesive mechanism. The relevant regulatory base for indirect food packaging adhesives is FDA 21 CFR 175.105; European sales require REACH Regulation (EC) No 1907/2006 and, for electronic assembly applications, RoHS Directive 2011/65/EU. Typical addition ratios in a packaging hot-melt formula place G1652 M at 15–30 wt%, a fully hydrogenated hydrocarbon tackifier at 40–55 wt%, a paraffinic or naphthenic white oil at 10–20 wt%, and a primary antioxidant plus secondary phosphite at 0.5–1.0 wt%. The processing sequence uses a jacketed sigma-blade mixer at 170–190 °C under a nitrogen blanket: the polymer is masticated first, tackifier is added in 3 sequential charges to avoid viscosity collapse, and oil is introduced only after the tackifier has been absorbed into the rubber phase. Slot-die coaters then apply the adhesive at 150–170 °C with coat weights of 15–50 g/m²; roller and bead applicators for case sealing typically operate at 160–180 °C. The creep failure inversion referenced in the heading is an operational boundary observed in hot-melt coating trials: above 180 °C application temperature, the endblock network becomes increasingly mobile, and ASTM D4498 shear adhesion failure temperature values fall from the 85–95 °C range to the 70–80 °C range when tackifier loading exceeds 50 wt%, because the tackifier begins to associate with the styrene domains rather than remaining exclusively in the ethylene-butylene/oil phase. The formulation window is therefore constrained at both ends—below 150 °C the adhesive cannot be coated uniformly, while above 180 °C the loss of cohesive strength reduces case-sealing stack performance in warehouses above 40 °C. Process operators quantify the effect by measuring viscosity on a Brookfield Thermosel at 177 °C and adjust tackifier aromaticity or lower oil content by 2–5 wt% rather than increasing pump temperature. Published data for this specific grade in pressure-sensitive adhesive configurations is limited, so the shear adhesion failure temperature shift should be verified on the exact formulation rather than inferred from general SEBS behavior. Terminal finished product types include carton and case sealing adhesives, multi-layer label adhesives, nonwoven construction adhesives for hygiene articles, and removable medical tape adhesives.
For two-shot and insert-molded grips on consumer durables, G1652 M is compounded into a TPE that is overmolded onto polypropylene, polycarbonate, or ABS substrates; this scenario is distinct from automotive interiors because adhesion must survive dishwashing, perspiration, hand creams, and UV exposure rather than VDA emissions. Compliance for consumer articles is defined by REACH Regulation (EC) No 1907/2006, RoHS Directive 2011/65/EU, and, for kitchen tools or reusable food-contact grips, FDA 21 CFR 177.2600 or EU 10/2011/EC overall migration below 10 mg/dm². The formulation addition ratio in a 40–70 Shore A grip compound loads SEBS at 30–45 wt%, PP at 15–25 wt%, white oil at 25–40 wt%, and calcium carbonate or silica filler at 0–10 wt%. Molding is performed on multi-shot injection-molding machines with melt temperature 190–230 °C, mold temperature 30–60 °C, and injection speed of 50–150 mm/s; pre-drying at 80 °C for 2 h is required when ambient relative humidity exceeds 60%. Adhesion to PP is process-sensitive: substrate temperature below 40 °C reduces surface-chain interdiffusion, and mold release agents on polycarbonate must be removed before overmolding. Terminal finished product types are power-tool handles, toothbrush grip zones, kitchen utensil handles, smartphone case edges, and personal-care device grips.
Flexible cable insulation and jacketing based on G1652 M enter a thermally constrained process regime when aluminum trihydroxide or magnesium dihydroxide is loaded sufficiently to meet flame-spread requirements. Cable compounds in this class must demonstrate compliance with IEC 60332-1-2 for vertical flame propagation on single insulated conductors, IEC 60754-2 for absence of corrosive halogen, IEC 61034-2 for smoke density with transmittance typically above 60%, ISO 6722 for automotive primary wire, SAE J1128 for low-tension primary cable, and UL 62 / UL 1581 for flexible cords and wires in North America. Formulation addition ratios place the SEBS at 20–35 wt%, a polyolefin diluent such as LLDPE or PP at 5–15 wt%, ATH or MDH at 40–60 wt%, paraffinic process oil at 5–15 wt%, an organosilane coupling agent at 0.5–1.5 wt%, and a stabilizer package at 0.5–2 wt%. The mixing step is frequently done in a Buss kneader or a reciprocating single-screw compounder at 160–200 °C rather than a high-shear twin-screw extruder, because the mineral filler decomposes at 190–210 °C and liberates water, causing microvoids and spark test failures in the final insulation. Twin-screw compounding is possible only when the melt temperature is held below 200 °C, screw speed is reduced to 200–300 min⁻¹, and vacuum venting at -0.06 to -0.08 MPa removes surface moisture before the die. The compounded pellets are then extruded onto conductors through a 25:1 L/D single-screw cable extruder with barrel temperatures of 170–195 °C, a crosshead die at 200 °C, and a water trough at 20–40 °C; drawing speed is set to maintain insulation outside diameter tolerance of ±0.05 mm. The principal production failure mode is surface porosity and die lip build-up when the melt exceeds 205 °C or when filler moisture exceeds 0.1 wt% after drying. Published data for this specific grade in high-halogen-free filler loadings is limited, so flame-spread behavior must be verified on each finished cable construction. Terminal finished product types include automotive battery cable insulation, appliance internal wire, flexible cord jackets, and low-smoke building wire jackets.
In polypropylene and polyphenylene ether/polypropylene blends, G1652 M is dispersed as a discrete elastomeric phase to raise low-temperature impact resistance without eliminating processability. Mechanical acceptance is anchored to ISO 180 notched Izod, ASTM D256 notched Izod, ISO 527-2 tensile properties, ISO 178 flexural modulus, ISO 75 heat deflection temperature, and ISO 306 Vicat softening temperature. The addition ratio for polypropylene toughening is typically 5–20 wt%; for PPE/PP automotive under-hood blends, 5–15 wt% is used because higher loadings lower the heat deflection temperature under ISO 75. Compounding is performed on a 40:1 L/D co-rotating twin-screw extruder at 200–230 °C for polypropylene and 230–260 °C for PPE-containing matrices, with a screw speed of 300–500 min⁻¹ to generate shear rates above 200 s⁻¹; fine rubber particle size is maintained by feeding SEBS into the main throat and matrix PP later if a high shear mixing bed is required. When the SEBS content exceeds 20 wt% in polypropylene, notched Izod impact is typically at a plateau while flexural modulus declines by 10–20%; below 5 wt%, impact improvement is often negligible due to discontinuous dispersion. Terminal finished product types include appliance housings, automotive battery cases, under-hood connectors, and luggage shells.
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Kraton™ G1652 M is a linear triblock copolymer based on styrene and ethylene/butylene midblocks, with a nominal polystyrene content of 30 wt% and a diblock fraction below 1.0 wt%. The M designation carries a documentation and control package intended for regulated applications; it does not indicate a different molecular architecture from corresponding non-M grades. Representative lot values for the neat polymer include a specific gravity of 0.91 g/cm³ by ASTM D792-20, Shore A hardness of 65 by ASTM D2240-15, tensile strength at break of 31.0 MPa by ASTM D412-16, elongation at break of 500% by ASTM D412-16, 300% modulus of 4.8 MPa by ASTM D412-16, and melt flow rate of 5 g/10 min at 230°C under 5 kg load by ASTM D1238-20. These values are typical lot-to-lot targets for uncompounded resin and shift substantially when the polymer is oil-extended or blended with polypropylene.
| Property | Method | Typical value |
|---|---|---|
| Polystyrene content | Manufacturer normalized method | 30 wt% |
| Diblock content | Gel permeation chromatography | <1.0 wt% |
| Specific gravity | ASTM D792-20 | 0.91 g/cm³ |
| Melt flow rate | ASTM D1238-20 at 230°C/5 kg | 5 g/10 min |
| Hardness | ASTM D2240-15 | 65 Shore A |
| Tensile strength at break | ASTM D412-16 | 31.0 MPa |
| Elongation at break | ASTM D412-16 | 500% |
| 300% modulus | ASTM D412-16 | 4.8 MPa |
On a co-rotating twin-screw extruder with 40:1 L/D and side-stuffing at barrel zone 7, paraffinic oil is normally introduced after the first kneading block. Early injection at zone 4 can lubricate the pellets before fluxing and create screw slip; late injection at zone 9 shortens residual mixing but may increase surface oil bloom in cooled pellets. For a target hardness of 30–40 Shore A by ASTM D2240-15, oil loading is commonly adjusted between 35 wt% and 50 wt% of the total hydrocarbon phase, depending on polypropylene melt flow and oil viscosity. Compression set measured at 70°C for 22 h by ASTM D395-18 often exceeds 45% when hardness drops below 40 Shore A; increasing polypropylene content or selecting a higher-viscosity oil raises hardness and lowers set but also reduces compound melt flow. Paraffinic oils above 100 cSt at 40°C demonstrate lower bleed tendency but require heated transfer lines and gravimetric metering accuracy of ±0.5 wt%. Batch-to-batch variance in pellet feed temperature can be larger than the oil-metering error; if condensation forms on chilled pellets at ambient humidity above 60% RH, the feed throat should be dehumidified or the pellets conditioned at 60–70°C for 2 h before gravimetric feeding, not because SEBS is hygroscopic but because surface moisture disturbs mass-flow control.
Regulatory standing for food-contact seals and medical-device components depends on finished-article testing rather than raw-polymer documentation alone. 21 CFR 177.1810 covers styrene block copolymers used as components in food-contact articles; EU Regulation 10/2011 imposes overall migration and specific migration limits on the final closure liner, gasket, or tubing. Cytotoxicity to ISO 10993-5:2009, hemolysis to ISO 10993-4:2017, and systemic reactivity to USP <88> Class VI are evaluations performed on the molded, cleaned, and sterilized device. The M-grade documentation suite supports design-history-file traceability and change control but does not replace process-validated biocompatibility data.
| Standard or regulation | Scope | Applicability statement |
|---|---|---|
| 21 CFR 177.1810 | Styrene block copolymers in food-contact applications | Use as a component; final article must satisfy extraction and migration requirements. |
| EU Regulation 10/2011 | Plastic food-contact materials | Overall migration and specific migration limits apply to the finished compound. |
| ISO 10993-5:2009 | Cytotoxicity of medical device materials | Testing required on the sterilized finished device, not on neat pellets. |
| USP <88> | Biological reactivity Class VI | Requires extraction of the final molded article under intended use conditions. |
| REACH 1907/2006 | Chemical registration and SVHC communication | Current safety data sheet and supplier SVHC declaration should be consulted for the shipped grade. |
In a hot-runner overmolding cell producing soft-touch grips on a polypropylene substrate, the melt temperature for a G1652 M compound is typically maintained between 190°C and 210°C; valve-gated drops are held at 200–215°C. If the melt temperature exceeds 230°C, the styrene-rich domains that give the material its elastic recovery lose strength, and gate-vestige deformation increases during part ejection. Below 180°C, filling of thin-wall sections below 1.0 mm becomes inconsistent, particularly when the substrate is a high-crystallinity polypropylene with a freeze skin that quenches the overmolded layer. Mold temperature is generally set from 20°C to 40°C; higher temperatures improve weld-line coalescence but increase cycle time and can make demolding of soft parts dependent on release agents. On a 1,600 kN clamp machine with screw recovery times above 12 s, batch-to-batch color shift has been observed in white oil-extended compounds; this is attributed to thermal history in the barrel rather than pigment dispersion. Published data for this specific configuration is limited, and process limits should be established by short-shot, gate-seal, and residence-time studies on the production tool.
Production-scale compounding lines with fewer than 3 post-injection kneading zones can produce oil-stripped pellets with surface bloom. This failure is observed when the side-stuffer discharge pressure exceeds the melt-pressure retention capability of the downstream kneading block, resulting in free oil at the die face. Screw configurations with narrow disk-width distribution elements may not generate sufficient extensional stress to incorporate oil into the ethylene/butylene midblock; the result is a bimodal pellet mass with reduced mechanical consistency after injection molding. These effects are measured as an increase in extractable fraction after pellet-surface aging rather than as a change in the dry-pellet melt flow rate.
If a finished device is sterilized by gamma irradiation at doses between 25 kGy and 50 kGy, the saturated ethylene/butylene midblock of G1652 M resists chain scission better than unsaturated SBS but may still develop odor and yellowing in oil-extended formulations. Aromatically modified oils and certain phenolic stabilizers are more prone to discoloration under gamma exposure; paraffinic oils with low aromatic content and secondary antioxidant packages that include phosphite or hydroxylamine compounds are used when coloration is a rejection criterion. Autoclave sterilization at 121°C for 30 min tests the upper thermal stability of the compound; continuous use above 105°C in pressure-bearing applications is generally not recommended for uncompounded SEBS, and the final compound’s heat-deflection temperature must be measured under ISO 75-2:2013. Published data for this specific configuration is limited, so terminal sterilization compatibility should be evaluated on the final molded component under worst-case loading and wall thickness.
Solvent-borne coating and film casting with Kraton G1652 M use toluene, cyclohexane, or mixed aliphatic-aromatic systems. Solution viscosity at 25 wt% solids in toluene is typically reported near 1,800 mPa·s at 25°C using a Brookfield viscometer. This is considerably lower than the corresponding value for high-molecular-weight SEBS grades and is one reason G1652 M is used in solvent-based adhesives where high solids and sprayable viscosity are required. Solvent selection alters the solubility of the polystyrene end-blocks; toluene and cyclohexane both solvate the midblock and endblock, while hexane-rich systems may precipitate the polystyrene domains and produce gel-like rheology. Flash point, residual solvent, and extractables of the dried film are governed by the coating line’s drying profile and must be confirmed on the finished coated substrate.
G1652 M occupies the medium-flow, 30 wt% styrene segment of linear SEBS grades. Compared with G1650 M, a higher-molecular-weight linear SEBS commonly selected for high tensile strength and low compression set, G1652 M provides lower melt viscosity and better thin-wall filling; however, the lower molecular weight may reduce ultimate tensile strength and raise compression set in demanding elastic-recovery applications. Compared with low-styrene grades such as G1657 M, which contain a higher diblock fraction, G1652 M generally produces higher hardness in lightly oiled compounds and faster solidification on a cold mold. The low-styrene grades may accept higher oil loadings before bleeding but exhibit a lower upper service temperature in the styrene-rich domain region. Capillary rheometry over 100–1,000 s⁻¹ by ISO 11443:2021 and tensile testing on the intended compound are required for grade selection because the neat-polymer melt flow rate does not predict behavior in polypropylene-modified formulations.
Compared with styrene-butadiene-styrene block copolymers, the saturated midblock of G1652 M removes the main-chain unsaturation that causes ozone attack and thermal embrittlement. In accelerated weathering, unfilled SBS compounds often lose more than 50% of tensile strength after 500 h of QUV exposure by ASTM G154-16, while stabilized SEBS compounds may retain above 80% depending on the stabilizer package. This distinction is central when the application is outdoor soft-touch equipment or automotive interior parts. Compared with peroxide-cured EPDM, G1652 M does not require sulfur or peroxide vulcanization and can be processed on thermoplastic equipment; however, the upper continuous-use temperature in hot-oil environments remains lower than that of a vulcanized ethylene-propylene network.
Medical tubing and respiratory mask cushions are usually not processed neat; they use a compound containing G1652 M, polypropylene homopolymer, white mineral oil, and sometimes 20–40 wt% barium sulfate for radiopacity. Radiopaque compounds may show specific gravity of 1.15–1.35 g/cm³ and reduced elongation, with final values determined on the molded article. For overmolded grips, adhesion to polypropylene is achieved by co-melting at the interface; substrate surface temperature must exceed the polypropylene crystallization temperature and remain above 140°C during injection. Published data for this specific configuration is limited, and adhesion should be measured by peel testing on the production tool rather than assumed from solubility parameters.