| HS Code | 679991 |
| Polymer Type | linear triblock styrene-butadiene-styrene block copolymer |
| Styrene Content | 31 wt% |
| Butadiene Content | 69 wt% |
| Density | 0.94 g/cm³ |
| Melt Flow Rate | 3.0 g/10 min at 200 °C/5 kg |
| Shore A Hardness | 70 |
| Tensile Strength | 22 MPa |
| Elongation At Break | 700% |
| 300 Modulus | 3.0 MPa |
| Tear Strength | 30 kN/m |
| Solution Viscosity | 3.5 Pa·s at 25% in toluene |
| Volatile Matter | ≤0.5 wt% |
| Ash Content | ≤0.2 wt% |
| Color | white |
| Form | pellet or powder |
As an accredited LCY Chemical Taiwan Globalprene® SBS 4601 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | LCY Globalprene® SBS 4601 is supplied in 25 kg polyethylene-lined paper bags, 40 bags per 1,000 kg pallet. |
| Container Loading (20′ FCL) | Loading a 20′ FCL container with LCY Chemical Taiwan Globalprene® SBS 4601, packaged and secured for ocean shipment. |
| Shipping | LCY Chemical Taiwan Globalprene® SBS 4601 is a non-hazardous thermoplastic elastomer typically shipped in 25 kg PE-lined bags or 1,000 kg jumbo bags on pallets, in dry containers by sea or land. Normal freight; no special dangerous-goods class. Keep cool, dry, ventilated; avoid sunlight, moisture, and ignition sources. |
| Storage | Store Globalprene® SBS 4601 in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, flames, and oxidizing agents. Keep containers tightly closed and protect from moisture and contamination. Avoid prolonged storage at elevated temperatures, use first-in, first-out rotation, and follow the supplier SDS and local regulations. |
| Shelf Life | The shelf life of LCY Chemical Taiwan Globalprene® SBS 4601 is generally 24 months under dry, cool, ventilated storage in unopened original packaging. |
In polymer-modified bitumen for heavy-duty asphalt, the styrene-butadiene-styrene architecture of Globalprene® SBS 4601 from LCY Chemical Taiwan develops a continuous three-dimensional network within the maltene phase when the binder is held at 170–185 °C under high-shear mixing. Plant-scale experience on rotor-stator mills operating at 3,000–5,000 rpm indicates that direct addition of pellets into bitumen below 160 °C results in incomplete particle swelling and visible gel agglomerates, forcing batch rejection or recycle. The binder formulation for load-bearing motorway surfaces typically incorporates 4.5–6.0 wt% 4601 based on total binder mass, while lower traffic-volume mixes use 3.0–4.5 wt%. The relevant framework is EN 14023:2010, which for PMB requires testing of softening point by EN 1427:2015, elastic recovery by EN 13398:2018, storage stability by EN 13399:2018, and low-temperature stiffness. In North America, product specification is often aligned with ASTM D5976/D5976M-21 and state highway agency variants of AASHTO M 320. Process control should include post-digestion low-shear maturation for 2–6 h at 170±5 °C, because premature cooling below 160 °C raises yield stress in the finished PMB and leads to transfer pump cavitation. Sulfur-based crosslinking, when used as a stabilizer at 0.05–0.15 wt%, narrows the processing temperature window to 175–185 °C; above 190 °C uncontrolled chain scission of the polybutadiene midblock reduces elastic recovery below the 60% minimum often specified for high-stress membranes. If the supplied grade contains extender oil, batching software should subtract that mass fraction from the binder oil phase to avoid under-dosing. End products include porous asphalt wearing course binders, stone mastic asphalt for elevated heavy-vehicle corridors, bridge deck waterproofing binders, and high-temperature industrial floor mastics.
When 4601 is combined with a hydrocarbon tackifier melt, the formulation window for hot-melt pressure-sensitive adhesives usually places the polymer at 18–35 wt%, with C5/C9 hydrocarbon or hydrogenated rosin ester tackifier at 40–60 wt%, naphthenic or paraffinic oil at 10–25 wt%, and a hindered phenolic antioxidant at 0.5–1.0 phr. The styrenic domains of 4601 lose network integrity as melt temperature rises; therefore sigma-blade or planetary mixers are operated at 140–160 °C under a nitrogen blanket, and slot-die coating is maintained at 120–150 °C to avoid viscosity collapse and edge bead instability. Compliance for food-contact packaging adhesives falls under FDA 21 CFR 175.105, and depending on export jurisdiction, the formulation must satisfy REACH 1907/2006 and RoHS 2011/65/EU. Finished tape and label constructions are evaluated for loop tack by ASTM D6195-22, shear adhesion failure temperature by PSTC-107, and 180° peel by ASTM D3330/D3330M-04(2020). Coating line speed is normally limited by melt fracture at the die lip when the elastomer content exceeds 35 wt%; at that point, viscosity at 150 °C can rise beyond 40 Pa·s, causing streak formation on polyethylene terephthalate release liners. Batch-to-batch variation in the diblock content of the SBS influences tackifier partitioning and loop tack; incoming lots should be checked for melt mass-flow rate by ISO 1133-1:2022 at 190 °C/5 kg and for styrene content by FTIR. Terminal downstream products include pressure-sensitive labels, carton sealing tapes, diaper construction adhesives, and mounting tapes for automotive interior trim.
Direct injection of SBS 4601/EVA/LDPE compounds into multi-cavity sole moulds is normally carried out at melt temperatures of 160–185 °C, with clamp force requirements of 150–300 t for full-shot moulds. The formulation ratio for midsoles and wedge soles commonly comprises 20–50 phr 4601, 40–70 phr EVA, 10–25 phr LDPE, 1.5–3.0 phr azodicarbonamide blowing agent, 0.5–0.8 phr dicumyl peroxide, and 2–5 phr zinc stearate. When the 4601 content approaches 50 phr, the styrene-block physical crosslinks increase low-shear melt viscosity and produce gate freeze at thicknesses below 1.2 mm, causing short shots in intricate tread patterns. Processing therefore uses a reverse temperature profile from feed throat 150 °C to nozzle 175 °C, with fast injection speeds of 80–120 mm/s and hold pressures of 50–80 MPa. Amine-based additives are excluded because they scavenge free radicals from the peroxide crosslinking step and destabilize the blowing agent decomposition profile. Compliance obligations for footwear exported to the EU include REACH Annex XVII restrictions on polycyclic aromatic hydrocarbons and phthalates; abrasion resistance is evaluated by ISO 20871:2018, flex fatigue by ISO 17707:2005, and tensile properties by ISO 37:2017. Terminal components include shock-absorbing midsoles, slip-resistant outsoles, sports sandal footbeds, and safety footwear heel inserts.
| Downstream segment | Primary standard/method | Controlled parameter | Typical acceptance band |
| Polymer-modified bitumen | EN 14023:2010 with EN 1427:2015 | Softening point | ≥ 60 °C high-stress PMB |
| Polymer-modified bitumen | EN 13398:2018 | Elastic recovery at 25 °C | ≥ 70% heavy traffic |
| Hot-melt PSA | FDA 21 CFR 175.105 / ASTM D6195-22 | Loop tack / peel | Application-specific |
| Footwear sole | ISO 17707:2005 / ISO 20871:2018 | Flex cut growth / abrasion | Application-specific per substrate |
| TPE grip | EN 71-3:2019+A1:2021 | Element migration | Element-specific limits |
| Waterproofing membrane | ASTM D6164/D6164M-21 / EN 1109:2013 | Low-temperature flexibility | No cracking at specified temperature |
| Recycled PP impact | ISO 180:2023 / ISO 178:2019 | Notched Izod / flexural modulus | Application-specific; laboratory reference ≥ 10 kJ/m² where specified |
For soft-touch thermoplastic elastomer grips, 4601 is typically let down in a co-rotating twin-screw extruder with an L/D ratio of 40:1 to 52:1, where process oil is injected through a side-stuffer at barrel zone 6–8 to prevent screw slip. The compound composition generally includes 40–75 wt% 4601, 10–25 wt% polypropylene, 20–40 wt% paraffinic/naphthenic process oil, and 0–10 wt% calcium carbonate or talc filler. The twin-screw barrel is set to 160–200 °C; exceeding 200 °C in the final two zones initiates oxidative degradation of the unsaturated polybutadiene midblock, producing surface tack and discoloration. Underwater pelletizing requires melt filtration through a 100–200 mesh breaker plate, and pellet drying to below 0.05% residual moisture before secondary injection moulding. Articles intended for repeated skin contact in toys are tested against EN 71-3:2019+A1:2021 migration limits, while US-bound toys are subject to ASTM F963-23. If the moulded article is intended for repeated food-contact use, the compound must comply with FDA 21 CFR 177.2600. Terminal products include overmoulded toothbrush handles, screwdriver grips, appliance knobs, and automotive interior storage mats.
If a bituminous waterproofing membrane formulation substitutes 4601 for EVA, the compound's low-temperature flexibility improves because the polybutadiene midblock has a glass transition well below -20 °C, but the mixing temperature must be raised from typical EVA ranges to 140–160 °C. The addition level for torch-applied membranes is generally 8–15 wt% SBS 4601 based on total bitumen compound; self-adhered membranes use 10–20 wt% to maintain peel at substrate temperatures as low as 5 °C. Production is carried out on continuous spread-coating lines in which a polyester or glass-fibre carrier is immersed in the hot compound and then calendered to the target thickness, usually 1.5–4.0 mm. Overhead infrared heating after coating drives off volatile process oils in an exhaust-controlled tunnel. Compliance for polymer-modified bitumen sheets is established under ASTM D6164/D6164M-21 for styrene-butadiene-styrene modified bituminous sheet materials, ASTM D1970/D1970M-20 for self-adhered underlayment used as ice barrier, and EN 13707:2013 for flexible sheets for roof waterproofing. Process technicians monitor low-temperature flexibility by EN 1109:2013 and peel adhesion by ASTM D903-98(2017). Terminal products include bridge-deck membranes, plaza-deck waterproofing, below-grade foundation sheets, and roof underlayment.
Recycled polypropylene impact modification uses 4601 at 5–15 wt% into a co-rotating twin-screw compounder, frequently with 2–5 wt% maleic anhydride-grafted polypropylene to improve interfacial wetting at the styrenic domains. The extrusion profile uses barrel temperatures from 180 °C at the feed section to 220 °C at the die, with screw speeds of 300–600 rpm and a throughput that avoids specific mechanical energy input above 0.25 kWh/kg. Under these conditions, the SBS phase disperses as discrete elastomer particles in the recycled PP matrix, and laboratory moulded specimens can reach notched Izod impact values above 10 kJ/m² when tested by ISO 180:2023; published data for this specific LCY grade diluted in post-consumer recycled PP is limited, so matrix contamination level remains the dominant variable. The performance gain plateaus above 15 wt% because the continuous styrene domains begin to reduce flexural modulus, measured by ISO 178:2019, and increase heat distortion under load. The modified compound is specified under ISO 19069-2:2016 for polypropylene moulding and extrusion materials, and must comply with RoHS 2011/65/EU for electrical applications. Terminal products include automotive interior trim, battery housings, appliance casings, and outdoor furniture components.
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LCY Chemical Taiwan supplies Globalprene® SBS 4601 as a linear styrene-butadiene-styrene block copolymer, CAS 9003-55-8, supplied in off-white porous pellet form. The grade is classified as a high-styrene SBS, with nominal styrene mass fraction reported as 40 wt% by ASTM D5775. This composition places the product between conventional medium-styrene SBS grades and harder styrenic block copolymers. At ambient temperature the polystyrene end-blocks form physical crosslinks in a continuous polybutadiene matrix, giving thermoplastic elastomer behavior without vulcanization. Typical primary packaging includes 20 kg multiwall paper bags and 500 kg bulk bags. Storage before processing must avoid direct sunlight and sustained temperatures above 35°C because oxidative degradation of the unsaturated butadiene segment accelerates under heat and ultraviolet exposure.
The polymer is used in bitumen modification, hot-melt adhesives, sealants, footwear compounds, and impact modification of thermoplastics. Its high styrene content produces higher hardness, higher cohesive strength, and greater heat resistance than 30 wt% styrene linear SBS, but it also increases melt viscosity and reduces low-temperature flexibility. The grade is not recommended for applications requiring high oil loading above approximately 30 wt% naphthenic oil, because phase separation and oil bleeding become process risks. Published data for every end-use configuration is limited; formulation trials should be run against the current supplier technical data sheet and batch certificate of analysis.
High styrene content shifts the melt processing window upward when compared with 30 wt% styrene SBS. Compounding is performed on co-rotating twin-screw extruders with L/D ratios between 32:1 and 48:1. Barrel temperature profiles from feed throat to die are maintained between 150°C and 195°C, with die temperature held at 180–190°C. Residence time is kept below 90 s to limit thermal degradation. Prolonged exposure above 210°C initiates butadiene double-bond oxidation and gel formation; gel particles appear as hard specks in extrudate and reduce adhesive clarity. On production-scale lines, pressure spikes at the screen pack are observed when the screw contains insufficient distributive mixing elements or when screw speed is too low to break down high-styrene domains. Screw speeds of 250–350 min⁻¹ with kneading blocks and combing mixers are typical for uniform dispersion.
Pre-drying is required at 70–80°C for 2–3 h when pellets have been exposed to relative humidity above 60% RH. Surface moisture causes splay and delamination in molded parts. A stabilizer package of 0.1–0.3 wt% hindered phenolic primary antioxidant and 0.1–0.3 wt% organophosphite secondary antioxidant is added to protect the unsaturated midblock during compounding. The grade is incompatible with strong oxidizing acids and with highly polar polymers such as unmodified PVC at high addition levels; compatibilizers are required to prevent delamination. Avoid free aromatic amine additives, which can accelerate discoloration and oxidative degradation of the butadiene segment.
Bitumen modification is evaluated through penetration, softening point, elastic recovery, and storage stability. SBS 4601 is typically added to paving-grade bitumen at 3–5 wt% polymer content. High-shear mixing at 180–190°C for 60–90 min disperses the polymer into a continuous bitumen-rich phase. Rotor-stator mixers with tip speeds of 15–20 m/s are used to achieve particle-size reduction. High styrene content raises the softening point and elastic recovery of modified bitumen, but it also raises mixing viscosity and pumping pressure. At 4 wt% polymer addition, elastic recovery at 25°C per ASTM D6084 commonly exceeds 70%. Storage stability is assessed per EN 13399; formulations with excessive polymer or insufficient mixing show phase separation and top-layer polymer enrichment after 3 days at 180°C. Addition of 0.5–1.0 wt% sulfur or reactive ethylene terpolymer stabilizes morphology, but overdose above 6 wt% polymer can cause gelation and loss of pumpability.
The high-styrene structure produces a harder modified bitumen and better rutting resistance than medium-styrene SBS at equal polymer loading. However, the low-temperature flexibility of the paving mixture is governed by the polybutadiene midblock; grades with 30 wt% styrene may be preferred in climates with sustained sub-zero temperatures. For SBS 4601, blend viscosity limits storage tank temperatures to approximately 190°C; above this threshold, thermal cracking of the bitumen accelerates and the polymer degrades.
Hot-melt adhesives formulated with Globalprene® SBS 4601, hydrocarbon tackifier, and naphthenic oil exhibit higher cohesive strength and elevated temperature resistance than equivalent 30 wt% styrene SBS compounds. The higher polystyrene endblock concentration increases upper service temperature, but it also raises application viscosity. A typical starting formulation range contains 20–35 wt% SBS 4601, 40–55 wt% hydrocarbon tackifier, and 15–30 wt% naphthenic oil. Ring-and-ball softening point measured by ASTM E28 typically increases by 5–10°C when SBS 4601 replaces a medium-styrene SBS at equal polymer content. Viscosity at 180°C is controlled by oil content; low-SBS high-styrene compounds may require 0.2–0.5 wt% paraffin wax to reduce stringing and improve clean cutting.
Low diblock content favors cohesive strength and shear resistance. SBS 4601 is specified with diblock content below 1 wt% by supplier internal method. Incoming quality-control tests should include solution viscosity at 25 wt% in toluene and melt flow rate, because batch-to-batch variation in diblock content shifts adhesive tack and cohesive strength. Solvent-based adhesives use toluene or cyclohexane; solution viscosity at 25 wt% solids is used as a molecular-weight indicator. High diblock content increases tack but lowers shear resistance, so grades with higher diblock content are not direct substitutes. Polar tackifiers such as rosin esters may phase-separate; hydrocarbon tackifiers with appropriate solubility parameters are required. Solvent-free hot-melt processing is performed at 170–190°C; above 200°C, gel formation accelerates and char deposits accumulate on application heads.
Compared with LCY medium-styrene linear grades, SBS 4601 provides higher hardness, higher cohesive strength, and higher heat resistance, but lower elongation at break and higher melt viscosity. Compared with LCY low-viscosity SBS grades used for transparent plastic modification, SBS 4601 has higher tensile strength and requires more intensive mixing. Compared with SEBS, CAS 66070-58-4, SBS 4601 retains unsaturated butadiene double bonds and requires antioxidant and UV stabilizer packages. It is not appropriate for long-term outdoor exposure above 80°C without suitable stabilization.
Table 1 lists representative supplier-published property ranges for Globalprene® SBS 4601. The ranges are not batch guarantees; verification against the current technical data sheet is required before specification. Hardness and tensile values are sensitive to specimen preparation. Compression molding at 160°C for 10 min followed by conditioning at 23°C and 50% RH for 24 h is typical before testing. Tensile properties are measured on die-cut specimens per ASTM D412-16 at 500 mm/min. Hardness is measured after 15 s per ASTM D2240. Melt flow rate is measured at 200°C/5 kg per ASTM D1238 or ISO 1133-1:2022. High-styrene SBS exhibits die swell and melt fracture at high shear rates; melt flow values above 10 g/10 min are not typical for this grade.
| Property | Test Method | Representative Range |
|---|---|---|
| Styrene content | ASTM D5775 | 38–42 wt% |
| Specific gravity | ASTM D792 | 0.94–0.96 |
| Melt flow rate, 200°C/5 kg | ASTM D1238 / ISO 1133-1:2022 | 0.5–5 g/10 min |
| Tensile strength | ASTM D412-16 | 18–22 MPa |
| Elongation at break | ASTM D412-16 | 500–650 % |
| 300% modulus | ASTM D412-16 | 2.5–4.0 MPa |
| Hardness | ASTM D2240 | 88–93 Shore A |
| Diblock content | Supplier internal method | <1 wt% |
The high styrene content reduces elongation and raises modulus when compared with 30 wt% styrene SBS. Grade selection should therefore be based on the required balance of heat resistance and low-temperature flexibility. Melt viscosity increases with styrene content, so injection molding and adhesive application temperatures must be adjusted upward. However, the processing window remains narrow: lower temperatures produce incomplete melting and undispersed polystyrene domains, while higher temperatures accelerate oxidative gel formation.
Footwear sole compounds based on SBS 4601 are prepared by injection molding or compression molding. In multi-cavity sole molds, clamp force of 80–150 metric tons and injection pressure of 70–90 MPa are used; nozzle temperature is maintained at 180–190°C. The high-styrene block structure provides dimensional stability and abrasion resistance when blended with polystyrene and oil. Wet pellets create gate splay and delamination, so pre-drying at 70–80°C for 2–3 h is mandatory if storage humidity exceeds 60% RH. Plastic modification of polypropylene and polystyrene uses 5–15 wt% SBS 4601 to improve low-temperature impact strength. Dispersion in polypropylene is achieved by twin-screw compounding at 210–230°C. The unsaturated polybutadiene segment reduces ultraviolet stability; formulators add 0.2–0.5 wt% UV stabilizer and 0.1–0.3 wt% hindered phenolic antioxidant. Processing above 220°C in polypropylene can cause chain scission and a reduction in impact performance.
Table 2 summarizes regulatory and compliance areas relevant to the bulk polymer. Compliance of a finished article depends on the full formulation, including tackifiers, oils, stabilizers, and pigments. The polymer itself is not classified as hazardous under CLP; however, porous pellet dust can form combustible dust-air mixtures during pneumatic conveying. Local exhaust ventilation and bonded grounding are required in conveying lines.
| Regulatory Area | Standard or Regulation | Applicability Note |
|---|---|---|
| REACH | EU 1907/2006 | Polymer is exempt from registration; constituent monomers must be registered by the supplier. |
| RoHS | Directive 2011/65/EU | Bulk polymer typically contains restricted heavy metals below 0.1 wt%; final article compliance is formulator-dependent. |
| FDA food contact | 21 CFR 177.1810 | Styrene block copolymers may be used subject to extraction limitations and end-use restrictions. |
| TSCA | 15 U.S.C. 2601 et seq. | Listed for commercial distribution in the United States. |
| China GB | GB 4806.6 | Food-contact use requires testing of the finished article, not only the polymer. |
In processing facilities, prolonged skin contact with molten polymer must be avoided. Thermal decomposition products include styrene monomer, butadiene, and low-molecular-weight hydrocarbons; local exhaust ventilation is required at die heads and application tanks. Storage life is generally 12 months from production date when kept in sealed original packaging below 35°C and protected from moisture. Material older than 12 months can be used only after re-testing melt flow rate, tensile strength, and solution viscosity against the original certificate of analysis. No conclusion or forward-looking statement is made regarding end-use suitability beyond these stated operational boundaries.