| HS Code | 347390 |
| Polymer Type | Linear triblock SEBS copolymer |
| Styrene Content | 32% |
| Specific Gravity | 0.91 |
| Melt Flow Rate | 11 g/10 min at 230 °C/5 kg |
| Shore A Hardness | 65 |
| Tensile Strength | 30 MPa |
| Elongation At Break | 600% |
| 300 Modulus | 3.5 MPa |
| Tear Strength | 30 kN/m |
| Solution Viscosity | 1,200 cP at 25 °C in 20% toluene |
| Volatile Matter | <0.5% |
| Antioxidant Content | Present |
As an accredited Kraton Kraton™MD SEBS MD6944 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ MD6944 SEBS is supplied in 25 kg multiwall paper bags, palletized for industrial handling and storage. |
| Container Loading (20′ FCL) | Kraton™ MD SEBS MD6944 is palletized and loaded into a 20′ FCL container, secured and evenly distributed for ocean shipment. |
| Shipping | Kraton™ MD SEBS MD6944 is shipped as dry, non-hazardous polymer pellets in sealed bags or boxes. It is not classified as dangerous goods; keep containers closed and protect from moisture, heat, and contamination. Follow local regulations and the manufacturer’s SDS for handling and transport. |
| Storage | Store Kraton™ MD SEBS MD6944 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and oxidizing materials. Keep containers or bags tightly closed to prevent moisture and contamination. Protect from prolonged UV exposure and avoid excessive stacking or damage to packaging. Use original packaging and follow the manufacturer’s SDS and local regulations for safe storage. |
| Shelf Life | Shelf life: 24 months from date of manufacture when stored in original sealed packaging under dry, cool conditions. |
In solvent-free cast film production for medical fluid-containment articles, MD6944 is dry-blended with a controlled-rheology polypropylene homopolymer and a paraffinic white oil before being metered into a 75 mm single-screw extruder with a 30:1 L/D barrier screw. The barrel profile is staged from 160°C in the feed zone to 195°C in the metering zone, with die temperature maintained between 205°C and 215°C to avoid melt fracture at film thicknesses below 0.15 mm. The saturated ethylene/butylene midblock removes the need for phthalate or citrate plasticizers, which is the primary technical driver when replacing flexible PVC in non-PVC IV bag outer film, pressure infusor sleeve, and procedure drape reinforcement lines. Typical formulation bands place MD6944 at 100 phr, polypropylene at 15-25 phr, and paraffinic white oil at 30-50 phr; higher oil levels reduce tensile strength but improve drape and low-temperature flexibility. The high styrene endblock content of 42 wt% contributes to room-temperature hardness and scuff resistance, while chill roll temperature is held at 18-25°C to prevent blocking. Film produced below 0.10 mm may require inline corona treatment at 34-42 dyn/cm for downstream printing or lamination. Extractable profiles are established on the finished article according to ISO 10993-12, not on the raw pellet, because sterilisation and lamination alter the extractables spectrum. Pre-drying at 70°C to a moisture level below 0.05 wt% is required when storage relative humidity exceeds 60%. The strain-hardening behaviour of the high-styrene endblock is exploited in deep-draw thermoforming of drainage bag films; however, the resin alone is not suitable for lipid-containing drug solutions unless extractables profiling and lipid sorption tests are completed. Terminal components are submitted for cytotoxicity, sensitisation, and irritation under ISO 10993-5, ISO 10993-10, and USP <88> testing on the final sterilised device contact layer. REACH and RoHS compliance remain compound-level obligations; the raw polymer manufacturer supplies the SVHC status for the unmodified pellet.
| End-use requirement | Test method | Endpoint |
|---|---|---|
| Biological reactivity in device contact layers | USP <88> | Class VI |
| Cytotoxicity of extract | ISO 10993-5 | Grade 0-1 |
| Sensitisation | ISO 10993-10 | No erythema or oedema |
| Extractables profile | ISO 10993-12 | Report per surface area and solvent |
| Repeated food-contact rubber article | FDA 21 CFR 177.1810 | End test on finished article |
Transparent tubing compounds based on MD6944 are processed through a 45 mm single-screw extruder fitted with a 25:1 L/D barrier screw and a crosshead die. The melt stream is delivered at 195-215°C into a vacuum calibration sleeve, where outer diameter tolerance is held to ±0.05 mm for tubing used in peristaltic pump sets. A typical dry blend contains 100 phr MD6944, 15-25 phr random polypropylene copolymer, and 35-50 phr medical-grade white oil; Shore A hardness is controlled by oil addition rather than by process temperature. The use of random copolymer instead of homopolymer reduces die-lip build-up at continuous run times above 8 h. Autoclave recovery is governed by endblock re-association after steam exposure; tubing at 121°C for 30 min shows temporary softening and must be allowed to cool under no tension to recover dimensional stability. Repeated cycles above 121°C or dry heat above 130°C produce surface tack and accumulation of low-molecular-weight oil on the inner lumen, which can be detected as an optical clarity shift before ISO 10993-5 extraction. Peristaltic pump tubing made from this compound is specified at 65-80 Shore A, with tensile strength and elongation measured by ISO 37 after 24 h conditioning at 23±2°C and 50±5% RH. For enteral feeding tubes, connection geometry is evaluated under ISO 80369-3; the compound does not ensure connector compliance unless the extruded tube is dimensionally stable after ethylene oxide sterilisation at 55°C and 60% RH. Incompatibilities include prolonged contact with polar solvents such as ketones and esters, which swell the styrene domains and reduce burst strength. Scale-up from laboratory cast film to production tubing requires full rheological characterisation with a capillary rheometer at 200°C and 210°C because the wall shear rate in the crosshead die exceeds typical film-die shear rates.
Injection-moulded diagnostics housings and auto-injector overmoulds based on MD6944 are produced from pre-compounded pellets rather than dry blends because the narrow process window at high styrene content demands consistent dispersion of polypropylene and oil. Compounding is carried out on a co-rotating twin-screw extruder with 40:1 L/D, atmospheric venting, and a melt temperature of 190-210°C; pelletised material is then dried at 70°C for 2-4 h before moulding. In the moulding cell, a 120-180 tonne clamp force press with a 30 mm screw is used. The melt temperature at the nozzle is maintained at 195-215°C, and the mould temperature is set to 20-40°C to promote rapid solidification of the high-styrene endblock phase. Gate geometry is sized at 0.8-1.2 mm for wall sections of 1.2-2.0 mm; gates below 0.6 mm are prone to premature freeze-off because the compound exhibits fast skin formation under high shear. Hot runner pressure drop increases with runner diameter below 4.0 mm; manifold temperatures above 220°C result in oil exudation and gloss variation on the part surface. Weld line strength is controlled by maintaining melt temperature above 195°C and injection velocity in the range 40-80 mm/s; lower velocities produce visible flow lines at the transition between rigid substrate and overmould. Shrinkage after 48 h at ambient conditions is 1.0-1.6%, which requires tool steel allowance adjustments relative to unfilled polypropylene. Terminal overmould compounds are evaluated for hardness by ISO 868, tensile properties by ISO 37, compression set by ISO 815-1 under 70°C/22 h and 23°C/72 h, and tear resistance by ISO 34-1. The compound is not suitable for thin-wall sections below 0.5 mm when injection pressure is limited to less than 80 MPa; mould fill simulations should be verified with short-shot studies at 80%, 90%, and 100% of predicted shot volume.
| Application | MD6944 (wt%) | PP homopolymer (wt%) | Naphthenic oil (wt%) | Target Shore A |
|---|---|---|---|---|
| Injection overmould grip | 45-55 | 20-30 | 20-30 | 60-70 |
| Medical housing seal | 50-60 | 25-35 | 15-25 | 70-80 |
| Low-stress clip | 40-50 | 30-40 | 10-20 | 80-88 |
At addition levels of 5-15 wt% in impact-modified polypropylene, MD6944 functions as a dispersed elastomeric toughener whose saturated ethylene/butylene midblock provides low-temperature crack-arrest capacity without the unsaturation-related oxidative instability of EPDM-based modifiers. The toughening mechanism is shear-yield activation ahead of the crack tip, not cavitation alone; for this reason, the upper loading bound is determined by flexural modulus loss rather than by impact plateau. A co-rotating twin-screw extruder with 40:1 L/D is used, with polypropylene pellets fed into the main throat and MD6944 fed through the throat or a downstream side feeder depending on screw design. Barrel temperatures from 180°C in zone 1 to 220°C in the later zones are used to keep the PP melt phase continuous; the SEBS phase requires adequate dispersive mixing at screw speeds of 300-500 rpm, but excessive specific energy above 0.25 kWh/kg can cause localized thermal degradation at the screw tips. Charpy notched impact strength is evaluated under ISO 179-1/1eA at -30°C, 0°C, and 23°C; multiaxial impact is evaluated under ISO 6603-2 with a 20 mm diameter striker. Terminal applications include automotive interior trim substrates, appliance fascia panels, and power-tool housing shells where low-temperature ductility is required. The compound is not intended for stiffness-critical structural components; at the upper 15 wt% loading, flexural modulus decreases sufficiently to require a 20-30% increase in part wall thickness if equivalent deflection resistance is specified. Pre-drying of MD6944 at 70°C for 2 h before compounding is recommended at relative humidity above 60%; entrapped moisture contributes to surface splay on subsequently moulded parts. Compounding trials on 40 mm and 65 mm twin-screw lines indicate that screw configuration and backpressure have a larger effect on Charpy scatter than the absolute MD6944 addition level within this window.
Elastic film laminates for wound care fixation tapes and disposable hygiene waistbands can be compounded from MD6944, a fully hydrogenated C5 tackifier resin, and a naphthenic or paraffinic process oil. The tackifier level controls the lower modulus plateau and peel adhesion to polyolefin nonwovens; typical starting points are 30-60 phr tackifier and 20-40 phr oil per 100 phr MD6944, but the tackifier softening point must be matched to the styrene endblock solubility parameter. A fully hydrogenated C5 resin with a softening point of 100-115°C minimises yellowing and odour compared to partly hydrogenated or aromatic-modified types. The compound is pelletised on a twin-screw extruder at 170-190°C before cast film extrusion through a slot die at 180-200°C; die temperatures above 210°C produce resin degradation and visible die-lip deposits within 4-6 h of continuous running. Film tensile properties are measured by ISO 527-3 on 0.05-0.15 mm thick film; hysteresis recovery is evaluated after 100% extension to 300% strain and is formulation-dependent. Blocking force increases with tackifier loading, and anti-block masterbatch at 1-3 wt% is normally required for roll stability above 0.10 mm thickness. The finished laminate is not suitable for sustained contact with low-polarity liquid solvents because the C5 resin phase can migrate to the film surface under pressure; terminal medical tape constructions require ISO 10993-5 and ISO 10993-10 assessment after adhesive coating and gamma sterilisation at 25-40 kGy.
For medical device cable jacketing, MD6944 is compounded with a halogen-free flame-retardant package based on magnesium dihydroxide or aluminium trihydrate, together with a polyolefin coupling aid. The mineral filler loading of 100-150 phr raises density and reduces surface gloss, but the saturated EB midblock retains flexibility at -20°C after 2,000 flex cycles; the finished construction is validated on the cable assembly rather than on the raw pellet. A 60 mm single-screw extruder with 30:1 L/D and a pressure-type die is used to apply the jacket at a melt temperature of 190-210°C; a 200-mesh screen pack is installed upstream of the die to remove agglomerates from the mineral filler. Wall thickness below 0.5 mm increases the risk of pinhole defects unless the compound is filtered at 40 µm and the die land length is at least 10 times the gap. Jacket hardness is typically 70-85 Shore A, with tensile strength, elongation, and tear measured according to ISO 37 and ISO 34-1 before and after ageing at 100°C for 168 h under ISO 188. Electrical safety testing is conducted on the finished cable according to IEC 60601-1 ancillary equipment requirements; the compound itself is not an electrical insulation system and is not assigned a dielectric strength without a defined cable construction. The material should not be exposed to autoclave sterilisation because the mineral-filled jacket may absorb moisture and develop surface blisters; ethylene oxide sterilisation is preferred. Terminal products include patient monitor cables, electro-surgical return lead jackets, and medical power cords where low halogen content and flexibility are specified.
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Kraton™ MD6944 is a neat styrene-ethylene/butylene-styrene block copolymer supplied as a free-flowing powder and classified within the SEBS family. Manufacturer documentation identifies the bound styrene content as approximately 13 wt%, with the balance consisting of a fully hydrogenated ethylene/butylene midblock. Because the midblock is saturated, the polymer does not contain the main-chain carbon-carbon double bonds present in SBS and therefore exhibits different oxidative, ozone, and thermal degradation behaviour. The neat specific gravity is approximately 0.91 when tested by ASTM D792. The product is not oil-extended and does not contain filler; it is positioned as a compounding base for flexible medical, personal care, and regulated thermoplastic applications. The low bound styrene content places MD6944 at the softer end of the SEBS spectrum relative to grades containing 30–33 wt% styrene. The practical result is lower room-temperature tensile modulus and hardness, with broader formulation latitude for plasticiser addition. Grade MD6944 should not be treated as interchangeable with another low-styrene SEBS without reviewing solution viscosity, diblock content, residual volatiles, and lot-release data from the supplier.
In MD6944 the styrenic end-blocks form glassy domains that act as physical crosslinks below the styrene glass transition. The approximately 13 wt% bound styrene content produces fewer load-bearing domains per unit volume than a 30 wt% styrene SEBS; the practical consequence is lower tensile stress at break and lower Shore A hardness when compared under ASTM D638 and ASTM D2240. Published mechanical data for low-styrene SEBS grades of this class generally show tensile strength in the range of 20–28 MPa and elongation at break above 700% for compression-moulded specimens; lot-specific MD6944 values should be taken from the supplier datasheet. The styrenic domains disassociate during melt processing, allowing the polymer to flow on conventional thermoplastic equipment. Single-screw extrusion of unfilled MD6944 is typically run at melt temperatures of 200–240°C on screws with an L/D ratio of at least 24:1 and a compression ratio of 2.5:1–3.5:1. Twin-screw compounding for filled or plasticised formulations is better performed on an intermeshing co-rotating extruder with L/D 32:1–48:1. Surface condensation is possible in high-humidity storage; material exposed to relative humidity above 60% should be pre-dried at 70–80°C for 2–4 h using desiccated air with a dew point below -20°C. Melt residence time above 260°C should be minimised to reduce chain scission, gel formation, and colour shift.
Medical tubing extrusion with MD6944 usually requires a formulated compound rather than neat resin. A compounder may add a high-viscosity white mineral oil to reduce hardness and a small amount of polypropylene to improve surface slip and tensile modulus. Oil addition at 50–120 phr can bring the compound into the soft Shore A region, while the polypropylene fraction controls dimensional stability and reduces blocking. A co-rotating twin-screw extruder with downstream oil injection is preferred for oil-loaded formulations because side-fed oil disperses more uniformly and reduces the risk of pellet surface oiling. On single-screw tubing lines, barrel profiles from 160°C in the feed section to 220°C at the die are typical for unfilled SEBS compounds. Pigmentation using polyolefin-compatible masterbatch is generally effective when adequate shear is available; poor dispersion is more often caused by insufficient backpressure or worn screw elements than by chemical incompatibility.
When compared with SBS, MD6944 resists oxidative embrittlement during melt recycling more effectively because the aliphatic midblock is saturated. When compared with high-styrene SEBS grades, the lower styrene content reduces stiffness and tensile strength rather than functioning as a direct indicator of melt viscosity. When compared with maleic anhydride-grafted SEBS, MD6944 has no anhydride functionality and will not bond reliably to polyamide or PET in coextrusion or overmoulding without a tie layer. This absence of polarity is significant for designers selecting between a neat SEBS and a functionalised SEBS for multi-material medical components.
SEBS polymers absorb aliphatic, cycloaliphatic, and aromatic hydrocarbons. MD6944 follows this behaviour; the saturated midblock swells in mineral oils and non-polar solvents, while ketones and short-chain alcohols are generally less aggressive. Solvent-bonding operations on extruded tubing should avoid aromatic or chlorinated solvents unless short contact times are validated for the specific wall thickness. Comparative swelling can be measured by immersion per ASTM D471 using IRM 901 oil for 24 h at ambient temperature; weight change and dimensional change should be recorded together because weight change alone can understate the effect of anisotropic swelling in extruded profiles. Plasticiser exudation becomes a risk when an oil-loaded compound exceeds the oil-holding capacity of the SEBS midblock. A high-molecular-weight paraffinic oil at 80–120 phr may appear dry immediately after compounding but can migrate to the surface during storage above 40°C. Compression set testing provides a better indication of network disruption than visual inspection, since surface bloom develops after internal phase separation has already begun.
Steam sterilisation at 121°C repeatedly subjects thin-walled tubing to temperatures near the styrenic end-block glass transition, which can produce dimensional distortion, kinking, or loss of interference fit. Ethylene oxide and gamma sterilisation are generally less thermally demanding, but radiation dose for MD6944 must be validated for the finished device. Published data for MD6944 under gamma irradiation is limited; therefore device manufacturers should plan dose-mapping studies under ISO 11137 rather than assuming generic SEBS radiation tolerance. Autoclave use is not appropriate for unmodified low-styrene SEBS devices without post-treatment dimensional testing and extraction verification.
Regulatory status for MD6944 is application-defined. Styrene-ethylene/butylene-styrene block copolymers are referenced in 21 CFR 177.1810 for food-contact rubber articles, but finished-device compliance depends on formulation, extraction testing, and end-use conditions. Cytotoxicity evaluation under ISO 10993-5 and hemocompatibility under ISO 10993-4 are outside the raw material datasheet; they are processing- and formulation-dependent. If a supplier certification to USP <88> Class VI is required, the specific lot documentation must be requested and matched to the final compound, because additives such as process oils, stabilisers, and masterbatch carriers can alter biological test results. No raw material statement transfers regulatory clearance to a finished article.
When MD6944 is compounded with calcium carbonate, talc, or silica, the low-styrene matrix may lose elongation more rapidly than a 30 wt% styrene SEBS because the filler particles replace elastomer volume and the glassy domain network is already sparse. Filled formulations above 20 wt% filler should be tested for tensile strength, elongation, and flexural modulus under ASTM D638 and ASTM D790. High-shear dispersion on a co-rotating twin-screw extruder with kneading blocks is required to prevent agglomerates; agglomerates act as stress concentrators and reduce tear resistance measured by ASTM D624. Filler addition also raises melt viscosity and may require a wider die gap to maintain tubing inner diameter during vacuum sizing.
When neat or compounded material is exposed to gamma radiation, the styrenic end-blocks may crosslink while the ethylene/butylene midblock may undergo chain scission; the net effect depends on dose rate, oxygen availability, and antioxidant package. Generic SEBS radiation data cannot be substituted for MD6944 validation. A dose of 25–50 kGy is common for medical devices, but the acceptable dose range must be established by the finished article under ISO 11137. If the product is to be used in a radiation-resistant formulation, addition of hindered phenols, phosphites, or radiation stabilisers may be necessary; the additive package must be selected to avoid interference with plasticiser migration, clarity, or extractables. Dose-rate effects are material-specific, so a single high-dose confirmation at low dose rate may not predict behaviour in high-speed gamma processing.
Differences from other SEBS products are primarily compositional and rheological. MD6944 is supplied as a neat resin with a controlled bound styrene level and powder particle size; oil-extended grades, in contrast, contain process oil at the point of sale and cannot be re-dried to a neat polymer. High-styrene SEBS grades provide higher tensile strength and hardness; maleated grades provide adhesion to polar substrates; high-flow grades may provide shorter cycle times but may sacrifice toughness. MD6944 is appropriate when the application requires a low-styrene base resin for soft, flexible, and processable thermoplastic compounds, but not when the part requires inherent adhesion to polar polymers or maximum tensile strength. In all cases, the compounder must control diblock content, molecular weight distribution, and residual monomer levels as part of lot acceptance, because these variables are not fully captured by a Shore A value alone. Differential scanning calorimetry can separate the ethylene/butylene midblock glass transition near -40°C from the styrenic end-block transition near 95°C, but it does not replace rheological and mechanical lot testing for finished compound consistency.