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Kraton Kraton™G SEP G1701 H

    • Product Name: Kraton Kraton™G SEP G1701 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 366166
    Product Name Kraton™ G SEP G1701 H
    Chemical Type Hydrogenated styrene-ethylene/propylene diblock copolymer
    Block Structure Linear diblock
    Polystyrene Content 37 wt%
    Density 0.92 g/cm³
    Melt Flow Rate 3 g/10 min at 230 °C/5 kg
    Shore A Hardness 70
    Tensile Strength 15 MPa
    Elongation At Break 700%
    300 Percent Modulus 2 MPa
    Solution Viscosity 1500 mPa·s at 25 wt% in toluene, 25 °C
    Volatile Matter ≤0.5 wt%
    Form Powder
    Appearance White powder

    As an accredited Kraton Kraton™G SEP G1701 H factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kraton™G SEP G1701 H is supplied in 25 kg moisture-resistant paper bags, palletized for convenient handling and storage.
    Container Loading (20′ FCL) 20′ FCL loaded with palletized 20 kg bags of Kraton™ G SEP G1701 H, shrink-wrapped, labeled, and secured for export.
    Shipping Kraton Kraton™G SEP G1701 H is shipped as a non-hazardous solid polymer in sealed, moisture-resistant bags or boxes. It is typically not regulated as dangerous goods. Store in a cool, dry, ventilated area away from sunlight, heat, and ignition sources; protect from moisture and contamination.
    Storage Store Kraton™ G SEP G1701 H in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep containers tightly closed to prevent moisture ingress and contamination. Avoid contact with strong oxidizing agents, protect from dust and physical damage, and follow first-in/first-out stock rotation.
    Shelf Life Typically 24 months from manufacture when stored in original, unopened packaging under dry, ambient conditions away from direct sunlight.
    Application of Kraton Kraton™G SEP G1701 H
    In transparent polypropylene compounds, the diblock architecture of styrene-ethylene-propylene copolymer such as Kraton G1701 H addresses the inherent trade-off between impact resistance and optical clarity that appears when conventional ethylene-propylene rubber modifiers are dispersed in random copolymer PP. The glassy styrene domain and ethylene-propylene midblock reduce dispersed-phase particle size and suppress visible light scattering; haze development is tracked on 1.2 mm injection-molded plaques under ASTM D1003-13, while tensile yield stress and elongation at break are evaluated under ISO 527-2 and notched impact under ISO 180. For rigid food-contact packaging and medical device housings, the starting formulation range is 15–25 wt% SEP diblock in a random copolymer PP carrier with a melt mass-flow rate of 15–25 g/10 min at 230°C/2.16 kg per ISO 1133-1. When flexible medical components are compounded from the same base resin, the addition level is commonly raised to 25–35 wt%, which reduces flexural modulus from the neat PP baseline while retaining sufficient cohesive strength for injection molding. The compounding operation runs on a co-rotating twin-screw extruder with an L/D ratio of 40:1, using a barrel profile from 190°C near the feed throat to 230°C at the die, a screw speed of 250–400 rpm, and a melt temperature setpoint that avoids the thermal-oxidative degradation threshold observed when local shear heating exceeds 250°C for prolonged residence times. Production-scale lines frequently record strand breakage when the die melt temperature falls below 190°C because the dispersed SEP domains have not fully softened; conversely, pellet agglomeration occurs when strand cooling water exceeds 25°C during extended runs. Pelletized compounds are subsequently processed by injection molding with a melt temperature of 200–230°C, a mold temperature of 20–40°C, and clamp force requirements calculated from cavity pressure for multi-cavity tools typically in the 80–150 t class for packaging components. Compliance documentation for food-contact applications requires that the formulated compound meets FDA 21 CFR §177.1810 for styrene block copolymers intended for repeated use, with extraction testing performed under 21 CFR §177.1520 olefin polymer requirements when polypropylene is the continuous phase; medical converters additionally screen the finished device under ISO 10993-5 and ISO 10993-10 because raw polymer certifications do not replace finished-device biocompatibility evaluation. Terminal products include clear refrigerator storage containers, over-the-counter pharmaceutical dispensers, diagnostic sample cups, and rigid medical trays where the combination of impact strength and contact clarity is specified by end-use quality plans.

    What Controls Viscosity Stability and Adhesive Transfer in SEP-Based Hot-Melt Pressure-Sensitive Adhesives?

    Hot-melt pressure-sensitive adhesives formulated with Kraton G1701 H use the diblock as a low-viscosity styrenic component to improve wet-out and coatability without the solvent burden of solution acrylic systems. The formulation window for transfer tape and label stock is typically 20–40 wt% SEP diblock, 40–60 wt% hydrogenated tackifier resin with a ring-and-ball softening point between 85°C and 105°C, 10–25 wt% white mineral oil or naphthenic oil, and 0.5–1.0 wt% hindered phenolic antioxidant plus phosphite stabilizer; diblock-rich formulations exhibit reduced viscosity at 160°C compared with triblock SEBS grades of similar styrene content, but they also show lower high-temperature cohesive strength and should therefore be blended with 10–20 wt% of a high-molecular-weight triblock when shear holding power is required. Mixing is carried out in a jacketed sigma-blade or planetary mixer under nitrogen blanket at 160–180°C with a total cycle time of 45–90 min; the stabilizer package is pre-dispersed in the oil phase to avoid oxidative degradation during prolonged hold at temperature. Batch-to-batch variation in tackifier softening point of ±2°C is a common source of coat-weight drift on slot-die lines, so tackifier is pre-screened by ring-and-ball softening point per ASTM E28-18 before batching. Coating on a slot-die line uses a delivery temperature of 150–170°C, a die-body temperature differential of ±3°C, and coat weights of 15–25 g/m² on silicone-coated release liners or direct-coated facestock. Adhesive performance is tested under PSTC-101 for peel adhesion at 180° peel angle, PSTC-107 for shear adhesion, and ASTM D3654-22 for loop tack, while retained viscosity after 72 h at 175°C is monitored as a thermal stability indicator. For indirect food contact, the formulated adhesive must comply with FDA 21 CFR §175.105; for toy and child-care applications, laboratory screening follows the EN 71-3 migration limits for elements, and finished-article testing is required because the raw polymer alone does not certify the final adhesive. Terminal products include clear double-sided tape, polyethylene film labels, hygiene construction adhesive, and transfer tapes used in graphic mounting where initial tack and thin-film clarity are purchasing specifications.
    ComponentTypical rangeFunction in adhesive
    Kraton G1701 H20–40 wt%Low-viscosity diblock backbone; tack and wet-out
    Hydrogenated tackifier40–60 wt%Pressure-sensitive tack development
    White mineral oil / naphthenic oil10–25 wt%Viscosity reduction; low-temperature flexibility
    Antioxidant / phosphite0.5–1.0 wt%Thermal-oxidative stabilization at mixing temperature
    A PVC-free medical film and tubing compound built around a polypropylene continuous phase and Kraton G1701 H diblock modifier is typically screened for replacement of flexible PVC where plasticizer migration is an operating restriction. The addition level of the SEP diblock to random copolymer PP sits in the 20–50 wt% band depending on Shore hardness targets; a 30 wt% loading in a cast-film grade PP with an MFR of 8–12 g/10 min at 230°C/2.16 kg under ISO 1133-1 yields a soft, clear film with reduced low-temperature brittleness, while higher loadings approach the viscosity limit of standard cast-film screw designs and require a low-compression screw with a water-cooled feed zone. Film production runs on a cast-film line with a die temperature of 210–230°C, chill-roll temperature of 15–25°C, and line speeds of 30–80 m/min; production-scale chill-roll sticking appears when the film web temperature at the nip exceeds 40°C, requiring a reduction in line speed or additional roll cooling. For tubing, a single-screw extruder with an L/D of 30:1 and a barrier screw is used at a melt temperature of 200–220°C before cooling in a water trough and cutting. Sterilization tolerance is a central specification because ethylene oxide exposure at 50–60°C for 4–8 h and gamma irradiation up to 25 kGy are common terminal sterilization routes; formulations must be evaluated for yellowing, tensile retention, and surface tack after sterilization per ISO 10993-5 cytotoxicity and ISO 10993-10 sensitization on the final article. Regulatory documentation requires that the polypropylene continuous phase meets the relevant 21 CFR olefin polymer status, while the styrenic block copolymer component is assessed under 21 CFR §177.1810 where applicable; no claim of inherent biocompatibility is made without device-level evaluation under ISO 10993-1:2018. Terminal products include oxygen delivery tubing segments, fluid drainage tubing, specimen transfer bags, and transparent medical packaging overwrap where the absence of ortho-phthalate plasticizers and latex proteins is specified by hospital supply contracts.
    Regulatory / test designationScope in medical film and tubing compounds
    ISO 10993-1:2018Final device biological evaluation planning; raw-polymer data not sufficient
    ISO 10993-5In vitro cytotoxicity of sterilized article
    ISO 10993-10Sensitization and irritation endpoints
    21 CFR §177.1810Styrene block copolymer component for food-contact; medical use requires additional device clearance
    ISO 1133-1Melt mass-flow rate control for incoming PP and compounded pellets

    When SEP Diblock Replaces Butyl Rubber in Solvent-Free Sealants

    Solvent-free sealant formulations that replace butyl rubber with Kraton G1701 H are developed for non-structural joint sealing applications in which migration resistance and long-term ultraviolet stability are more valued than high gas-barrier performance. The addition range is 10–25 wt% SEP diblock in a formulation comprising 20–35 wt% polyisobutylene, 20–30 wt% hydrogenated tackifier, 15–30 wt% calcium carbonate filler with a median particle size of 2–5 μm, and 0.5–1.5 wt% antioxidant/UV stabilizer. The SEP diblock is pre-compounded into a binder at 130–160°C in a planetary mixer with jacketed heat transfer, then filler is added under vacuum to reduce air entrainment and to achieve a final moisture content below 0.1 wt%; production-scale batches can show filler settling if vacuum is broken before homogenization is complete. Sealant extrusion and application behavior is tested by slump per ISO 7390:2003, tensile properties of the cured joint per ISO 8339, and adhesion-elongation under ISO 8340; construction sealants are classified under ISO 11600:2011 according to movement capability, while facade sealants may require EN 15651 test sequences. The operational boundary is explicit: SEP diblock-based sealants are not suitable for structural glazing or insulating glass edge seals because cohesive strength and argon permeation resistance are lower than reactive polyurethane or silicone systems. Terminal products include expansion joint sealants for concrete panels, automotive interior seam sealants, and vibration-damping bead formulations where low-temperature flexibility and low VOC emissions under VDA 277 are acceptance criteria.

    Low-Gloss Soft-Touch TPO Modification with SEP Diblock

    Thermoplastic polyolefin compounds for automotive interior surfaces use Kraton G1701 H as a modifier to adjust surface tactility and reduce the gloss of injection-molded polypropylene without the paint films historically used on rigid substrates. Addition levels in TPO compounds are lower than in packaging-grade flexible PP, typically 5–15 wt% SEP diblock in a blend of reactor-grade PP impact copolymer and ethylene-octene plastomer. The compound is prepared on a co-rotating twin-screw extruder with an L/D of 44:1 and side-feeding for mineral filler, using a barrel profile of 200–235°C, screw speed of 350–450 rpm, and vacuum venting at −0.08 MPa gauge to strip residual volatiles. Injection molding of interior panels requires a melt temperature of 210–240°C, injection speed profiling to avoid jetting at the gate, and a mold surface temperature of 20–40°C; gloss values are measured on 2 mm plaques at 60° geometry under ISO 2813 and compared against a matte-finish reference plate. Emission and odor compliance follows VDA 277 total VOC, VDA 270 odor classification, and DIN 75201 fogging; flammability is evaluated per FMVSS 302 or ISO 3795 where specified by the vehicle platform. Processors should not exceed melt temperatures of 250°C for residence times above 4 min, because molecular weight degradation produces a visible viscosity drop and gloss increase; production-scale lines with long hot-runner hold times therefore use lower temperature setpoints or purge sequences. Terminal products include door trim inserts, center console side panels, seat-back covers, and instrument panel lower elements where low-gloss, scratch-resistant surfaces are specified by the OEM material standard.For child-care and toy conversion, the same clear diblock modifier provides a tactile, low-hardness surface while retaining light transmission in injection-molded polypropylene. Addition levels in toy-grade PP are typically 20–35 wt%, with the balance selected from a high-clarity random copolymer PP and a slip/antiblock package; melt temperature during injection molding is maintained at 200–230°C, and hot-runner tools are operated with 2–5°C temperature variability across the manifold to reduce visible flow lines. Mechanical testing follows EN 71-1 physical and mechanical requirements, and chemical migration testing follows EN 71-3 for elements; food-contact status for utensils or oral-contact toys is not automatic and requires additional evaluation under 21 CFR §177.1520 for the polypropylene continuous phase and 21 CFR §177.1810 for the styrenic component. The production process is a standard twin-screw compounding step followed by injection molding, with no solvent-based coating or painting required; molds with polished cavity surfaces are used to preserve the low-haze appearance. Terminal products include transparent teething articles, toy action figure limbs, baby bottle overmolding grips, and puzzle components where the final article must pass tensile testing under ISO 527-2 on cut specimens. Published data for this specific configuration is limited; each converter must requalify the compound after any change in color masterbatch because pigment carriers can alter dispersed-phase particle size and reduce light transmission.
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    Certification & Compliance
    More Introduction

    Kraton™ G SEP G1701 H is a linear triblock copolymer composed of terminal styrene blocks and a hydrogenated ethylene/propylene midblock. The grade is supplied as low-dust pellets and is intended for melt-compounding operations in which saturated-midblock stability, optical clarity and mechanical toughness are simultaneous requirements. Under ISO 1183-1:2019 the specific gravity is 0.92. The melt flow rate determined under ISO 1133-1:2022 at 230 °C/5.0 kg is 1.0 g/10 min, indicating a relatively high-molecular-weight neat polymer that demands shear-driven melting rather than conduction-limited plastication. Because the material is not oil-extended, this melt flow rate and the mechanical properties measured on the neat copolymer are not directly transferable to formulated compounds. Principal use areas include clear films, polyolefin modification, low-extractable medical components, high-clarity adhesives and sealants. Finished-article compliance is compound-specific and must be confirmed by the converter or device manufacturer against the applicable regulatory schedule.

    What distinguishes Kraton™ G SEP G1701 H from other hydrogenated styrenic block copolymers?

    The saturated ethylene/propylene midblock is the primary structural variable separating G SEP G1701 H from unhydrogenated styrene-butadiene-styrene grades and from many SEBS products. The midblock lacks the main-chain unsaturation that in SBS elastomers contributes to thermo-oxidative chain scission and yellowing after repeated melt histories. At the same time, the ethylene/propylene architecture reduces the crystallinity associated with polyethylene midblocks, which supports low haze in thin-gauge films. Haze after compression moulding of 1 mm plaques is evaluated under ASTM D1003-21. The styrene content of 37 wt% places the grade in a higher-modulus region than Kraton G1702 H, which has a lower styrene content. Selection between these two grades is therefore governed by the required hardness, block-phase glass transition temperature and compound viscosity. G SEP G1701 H also produces lower melt flow than lower-molecular-weight SEPS grades, which improves tensile strength and puncture resistance but raises torque demand during compounding. Published data for direct comparative haze and compression set measurements on all equivalent formulations are limited; users should run paired compound trials under constant mixing energy and identical conditioning according to ISO 23529:2016 before changing grades.

    Phase separation of the styrene end-blocks creates a thermally reversible network of glassy domains. Under small-amplitude oscillatory shear, the crossover of storage modulus and loss modulus occurs within the processing window; this crossover can be measured with a parallel-plate rheometer at 200 °C under 1% strain. The zero-shear viscosity of the neat polymer is high relative to oil-extended grades, so slit-die measurements are preferred over capillary rheometry when wall slip is suspected. These rheological characterizations are performed on dried specimens under nitrogen to limit oxidative degradation during the frequency sweep. The triblock architecture produces pronounced stress upturn at high extension, which is typical of well-defined styrene microphase separation and distinguishes the product from random copolymers used as viscosity modifiers.

    Table 1 lists representative values published for neat polymer; these are not compound specifications. Compression-moulded specimens are conditioned for 24 h at 23 °C ± 2 °C and 50% ± 10% RH before mechanical testing. Hardness is measured on 6 mm plaques. Tensile tests use 2 mm die-cut specimens pulled at 500 mm/min.

    Table 1: Typical property envelope for Kraton™ G SEP G1701 H
    PropertyStandardTypical value
    Specific gravityISO 1183-1:2019 / ASTM D792-200.92
    Melt flow rateISO 1133-1:2022 / ASTM D1238-20, 230 °C / 5.0 kg1.0 g/10 min
    HardnessISO 868:2003 / ASTM D2240-1564 Shore A
    Tensile strengthISO 37:2017 / ASTM D638-2222.1 MPa
    Elongation at breakISO 37:2017 / ASTM D638-22750%
    300% modulusISO 37:20172.1 MPa
    Styrene contentInternal pyrolysis or NMR method37 wt%
    Diblock contentInternal GPC method<1%

    Processing constraints in high-shear compounding

    On a co-rotating twin-screw extruder with a screw diameter of 25 mm and an L/D ratio of 40:1, a graduated temperature profile is used: feed throat 30–40 °C, barrel zones 180–220 °C, and die head 200–210 °C. Because the neat melt flow rate is low at 1.0 g/10 min, melting is shear-driven rather than conduction-driven. Screw speed in the range 250–400 min⁻¹ is typical to hold melt temperature within the target; screw speed below 200 min⁻¹ can produce inhomogeneous block domain distribution in direct injection of neat polymer. Torque rise of more than 15% from baseline at constant throughput may indicate filler agglomeration, degraded material or insufficient plasticizer dispersion. Feed throat temperature must remain below 35 °C; pellet surface tack at elevated feed-zone temperatures can reduce screw filling and cause output fluctuation. The polymer itself is not highly hygroscopic, but hygroscopic additives such as talc, starch-based fillers or certain polar modifiers require pre-drying of the additive masterbatch to a moisture content below 0.05 wt% before entering the melt. Residence time above 250 °C should be kept below 3–5 min; longer hold-up can produce chain scission and discoloration, detected as an upward yellowness-index shift under ASTM E313-20.

    When this grade is incorporated into polypropylene at 10–20 wt%, the resulting blend exhibits a shift in impact failure mode from brittle crack propagation at low temperature toward ductile shear yielding. The specific improvement depends on the base polypropylene molecular weight, rubber domain size and processing history. In a 25 mm twin-screw compounding line, domain sizes between 0.5 μm and 2 μm are commonly targeted; transmission electron microscopy or atomic force microscopy is used to confirm morphology. Melt-blended compounds are typically conditioned for 48 h at 23 °C ± 2 °C before Izod notched impact testing under ISO 180:2019 or Charpy testing under ISO 179-1:2010. At addition levels above 30 wt%, haze in thin-wall injection-moulded parts may increase unless the base polypropylene is clarified or the rubber domain size is maintained below the wavelength of visible light. Published data for this specific configuration is limited; formulators should verify haze loss on moulded plaques of target thickness rather than relying on neat-polymer clarity.

    When clarity retention and low extractables are both required

    Clear film and medical component formulations demand more than haze control; the extraction of low-molecular-weight fractions into aqueous or lipid simulants can govern regulatory acceptance. G SEP G1701 H has a low diblock content, which reduces the concentration of loosely bound styrene-rich or midblock-rich chains that can migrate. For medical device components, extraction is performed according to ISO 10993-12:2021 with polar and non-polar simulants, and cytotoxicity is assessed under ISO 10993-5:2009. The saturated midblock resists the formation of oxidation products during gamma sterilisation at 25–40 kGy; nevertheless, yellowness index must be measured on the finished component because trace additives in the compound can dominate the irradiation response. For reusable consumer goods, repeated autoclaving at 121 °C for 30 min may produce no significant loss of tensile strength, but the sealing geometry and adhesive interface are the limiting variables. The polymer should not be used in contact with strong oxidising acids or with solvent systems containing high levels of methylene chloride, which can swell the styrene domains and reduce dimensional stability. Where low extractables are specified, the use of low-molecular-weight mineral oils is restricted because plasticizer migration in thin films can increase total organic carbon in leachates.

    Adhesive and sealant formulations containing this polymer are generally processed in sigma-blade mixers or co-rotating twin-screw extruders. The high molecular weight of the neat polymer increases cohesive strength and peel resistance but also raises hot-melt viscosity; tackifier resins and low-aromatic oils are used to adjust open time and wet-out. A starting formulation range of 30–60 parts per hundred rubber of hydrogenated hydrocarbon tackifier is common for high-clarity pressure-sensitive adhesives, although the exact optimum depends on the end-block reinforcing efficiency and the softening point of the tackifier. Peel adhesion on stainless steel can be measured under ASTM D3330/D3330M-09 after 24 h dwell; comparison between formulas is only valid when coat weight and backing film thickness are held constant. The saturated midblock permits lower stabilizer loading than SBS adhesives in indoor applications, but outdoor performance still requires a UV absorber and hindered amine light stabilizer combination. Users should not extrapolate neat-polymer clarity to filled or tackified systems without haze measurement on the final adhesive layer.

    Regulatory status and migration testing requirements

    Food-contact, medical and toy applications are not validated by neat polymer status alone. In end-use articles, compliance with FDA 21 CFR 177.1810 or EU 10/2011 requires finished-article migration testing because the overall migration limit of 10 mg/dm² under EN 1186 applies to the final structure, not to the raw polymer. Specific migration of styrene and lower oligomeric species is measured under EN 13130; results vary with layer thickness, food simulant, temperature and oil content. For toys, the relevant standards may include EN 71-3 for the migration of certain elements, although G SEP G1701 H does not contain heavy metals by design. Users should obtain the current regulatory data sheet from the supplier and validate each finished article because processing aids, pigments and adhesion promoters can alter the overall migration fingerprint. Published data for this specific configuration is limited; no universal compliance statement can be made for all applications.

    Table 2: Typical compliance and test methodology matrix for finished articles containing Kraton™ G SEP G1701 H
    Regulation / applicationTest methodEnd-user requirement
    Food-contact articlesEU 10/2011, FDA 21 CFR 177.1810Overall migration <10 mg/dm²
    Specific migrationEN 13130Styrene oligomer limits article-specific
    Medical device extractsISO 10993-12:2021Extract qualification per device risk class
    CytotoxicityISO 10993-5:2009End-user acceptance criterion
    Toy element migrationEN 71-3Element-specific limits

    The distinction between G SEP G1701 H and unhydrogenated SBS grades becomes most evident when the polymer is subjected to repeated melt processing or ultraviolet exposure. Unsaturated midblocks in SBS grades form carbonyl and hydroperoxide species during oxidation; these degradation products shift yellowness index and reduce tensile retention. The saturated ethylene/propylene midblock of G1701 H delays this pathway, although the material is not inherently stabilised and still requires an antioxidant package for long-term heat ageing. In contrast to oil-extended SEBS grades, G SEP G1701 H allows formulators to control oil type and loading rather than inheriting a fixed extender level. This characteristic is advantageous for low-extractables applications but increases formulation complexity and torque demand. Comparative selection therefore depends on whether the application is compound-dominated or polymer-dominated. End users evaluating a permanent grade substitution should establish equivalence on the production line, not only in laboratory plaques.

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