| 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 | 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. |
| Component | Typical range | Function in adhesive |
|---|---|---|
| Kraton G1701 H | 20–40 wt% | Low-viscosity diblock backbone; tack and wet-out |
| Hydrogenated tackifier | 40–60 wt% | Pressure-sensitive tack development |
| White mineral oil / naphthenic oil | 10–25 wt% | Viscosity reduction; low-temperature flexibility |
| Antioxidant / phosphite | 0.5–1.0 wt% | Thermal-oxidative stabilization at mixing temperature |
| Regulatory / test designation | Scope in medical film and tubing compounds |
|---|---|
| ISO 10993-1:2018 | Final device biological evaluation planning; raw-polymer data not sufficient |
| ISO 10993-5 | In vitro cytotoxicity of sterilized article |
| ISO 10993-10 | Sensitization and irritation endpoints |
| 21 CFR §177.1810 | Styrene block copolymer component for food-contact; medical use requires additional device clearance |
| ISO 1133-1 | Melt mass-flow rate control for incoming PP and compounded pellets |
Competitive Kraton Kraton™G SEP G1701 H prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8618005193850 or mail to sales8@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8618005193850
Email: sales8@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
| Property | Standard | Typical value |
|---|---|---|
| Specific gravity | ISO 1183-1:2019 / ASTM D792-20 | 0.92 |
| Melt flow rate | ISO 1133-1:2022 / ASTM D1238-20, 230 °C / 5.0 kg | 1.0 g/10 min |
| Hardness | ISO 868:2003 / ASTM D2240-15 | 64 Shore A |
| Tensile strength | ISO 37:2017 / ASTM D638-22 | 22.1 MPa |
| Elongation at break | ISO 37:2017 / ASTM D638-22 | 750% |
| 300% modulus | ISO 37:2017 | 2.1 MPa |
| Styrene content | Internal pyrolysis or NMR method | 37 wt% |
| Diblock content | Internal GPC method | <1% |
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.
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.
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.
| Regulation / application | Test method | End-user requirement |
|---|---|---|
| Food-contact articles | EU 10/2011, FDA 21 CFR 177.1810 | Overall migration <10 mg/dm² |
| Specific migration | EN 13130 | Styrene oligomer limits article-specific |
| Medical device extracts | ISO 10993-12:2021 | Extract qualification per device risk class |
| Cytotoxicity | ISO 10993-5:2009 | End-user acceptance criterion |
| Toy element migration | EN 71-3 | Element-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.