| HS Code | 502105 |
| Product Type | M6-M8 Hydrocarbon Resin for High-Speed CCL |
| Appearance | Pale yellow to amber granules |
| Softening Point Ring Ball | 100-130 °C |
| Melt Viscosity 200 C | 100-500 mPa·s |
| Number Average Molecular Weight Mn | 600-800 |
| Molecular Weight Distribution Pdi | 1.5-2.5 |
| Volatile Content 105 C 3 H | ≤ 0.5% |
| Acid Value | ≤ 0.5 mg KOH/g |
| Bromine Value | ≤ 20 g Br/100 g |
| Dielectric Constant Dk At 10 Ghz | ≤ 2.6 |
| Dissipation Factor Df At 10 Ghz | ≤ 0.0015 |
| Moisture Content | ≤ 0.1% |
| Glass Transition Temperature Tg | 50-70 °C |
| Color Gardner | ≤ 3 |
As an accredited M6-M8 Hydrocarbon Resin for High-Speed CCL - Sunmun Technology factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | M6-M8 Hydrocarbon Resin for High-Speed CCL from Sunmun Technology is supplied in 25 kg sealed drums for safe, stable handling. |
| Container Loading (20′ FCL) | 20′ FCL shipment of M6-M8 Hydrocarbon Resin from Sunmun Technology, packed in bags/pallets for high-speed CCL production. |
| Shipping | M6-M8 Hydrocarbon Resin ships in sealed drums or woven bags to prevent moisture contamination. Keep upright, dry, and away from heat/ignition sources. Standard freight or container transport is suitable. Avoid prolonged UV exposure and rough handling to maintain resin purity for high-speed CCL applications. |
| Storage | Store M6-M8 Hydrocarbon Resin in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep containers tightly sealed to prevent moisture absorption and contamination. Recommended storage temperature is below 30°C. Under proper conditions, shelf life is typically six months from manufacture date. |
| Shelf Life | Store in original sealed container, away from heat and moisture. Shelf life is 12 months from production date. |
In 800G-class switch-fabric line cards, the thermoset matrix is compounded with 15–28 wt% of Sunmun Technology M6-M8 hydrocarbon resin based on total organic solids. The hydrocarbon phase displaces a portion of the high-polarity resin fraction, reducing equilibrium moisture absorption to below 0.15% after 24 h at 23 °C under IPC-TM-650 2.6.2.1, while the cured dielectric constant remains in the 3.4–3.8 range at 10 GHz when measured by IPC-TM-650 2.5.5.9. Qualification for these cores follows IPC-4101E high-speed slash requirements, UL 94 V-0, and halogen-free criteria under IEC 61249-2-21. On a 2,200 mm wide horizontal treater running at 8–12 m/min, the hydrocarbon resin is predispersed into the PPE/TAIC varnish using a high-shear dissolver at 1,500–2,000 rpm; the resin bath is held at 55–65 °C with a working viscosity of 300–700 mPa·s to stabilize prepreg resin content between 55% and 68%. B-stage gel time at 171 °C is maintained at 150–190 s; a drift of more than 25 s within a production lot generally indicates miscibility drift or accumulated prepolymerization and requires a resin bath exchange. After lamination in a 20-opening vacuum press at 190–210 °C and 2.5–3.8 MPa, the core is processed into dielectric layers from 0.05 mm to 0.25 mm. Loadings above 28 wt% can decrease copper peel strength because the nonpolar hydrocarbon phase concentrates at the copper-resin interface; adhesion is therefore verified after thermal stress by IPC-TM-650 2.4.8 at a minimum of 0.8 N/mm. The terminal product is a 24–64-layer backplane or switch line card supporting 56–112 Gbps SerDes signaling.
| Property | Test method | Control band | Qualification gate |
|---|---|---|---|
| Dielectric constant at 10 GHz | IPC-TM-650 2.5.5.9 | 3.4–3.8 | Signal propagation consistency |
| Dissipation factor at 10 GHz | IPC-TM-650 2.5.5.5 | 0.0020–0.0040 | Insertion loss budget |
| Glass transition temperature by DMA | IPC-TM-650 2.4.24.4 | ≥ 180 °C | Solder reflow margin |
| Water absorption | IPC-TM-650 2.6.2.1 | ≤ 0.15% | CAF and dielectric constant stability |
| Copper peel strength after thermal stress | IPC-TM-650 2.4.8 | ≥ 0.8 N/mm | Plating adhesion |
| Flammability | UL 94 | V-0 or VTM-0 | Safety certification |
Prepreg bonding sheets in high-layer-count backplane manufacture impose a narrower rheological window than core lamination because the B-stage resin must flow enough to fill circuitry while retaining a stable melt-viscosity plateau at lamination pressure. M6-M8 hydrocarbon resin is metered at 10–22 phr relative to the total resin blend for bonding thicknesses from 0.08 mm to 0.15 mm; above 22 phr, the melt flow length during press rise can produce edge squeeze-out and thickness variation greater than ±5%, while below 10 phr the resin may not wet buried copper geometry with 25–50 µm line topography. The governing specification is IPC-4101E for prepreg used in rigid multilayer boards; incoming resin content is tested by IPC-TM-650 2.3.16, gel time by IPC-TM-650 2.3.18, and volatile content by IPC-TM-650 2.3.19. In production, a horizontal treater with 6–10 m/min line speed and four drying zones set at 120–180 °C is used; the as-coated prepreg is held to 58–70 wt% resin content and residual volatiles below 1.0%. The resin bath temperature tolerance is ±3 °C because the gel-time control window of 150–190 s at 171 °C is narrow; a recurrent failure mode on continuous treaters is gel-time shortening after 3–4 h due to prepolymerization in the dip pan, so hourly gel-time sampling and automatic solvent makeup are required. The treated prepreg is laid up with patterned cores in a vacuum-assisted multi-opening press and laminated at 180–200 °C and 2.4–3.4 MPa, with the pressure ramp delayed until the resin reaches 110–130 °C to avoid displacing glass and producing resin-starved dielectric gaps. The terminal product is a sequentially laminated 24–64-layer backplane bonding sheet used in modular data-center switch fabrics.
When the substrate operates at 26 GHz in a 5G massive MIMO active antenna unit, phase stability and moisture absorption become primary selection drivers because a 0.12 mm core with a dielectric constant variation of ±0.04 across the panel creates measurable beam pointing error. The M6-M8 hydrocarbon resin is optimized at 18–30 wt% of total organic solids to lower dielectric anisotropy while maintaining dimensional stability; the cured laminate is tested by IPC-TM-650 2.5.5.9 and IPC-TM-650 2.5.5.5 at 10 GHz and 28 GHz, with control bands of 3.4–3.8 for dielectric constant and 0.0020–0.0040 for dissipation factor. Moisture absorption is held below 0.12% by IPC-TM-650 2.6.2.1. The regulatory path includes IPC-4101E high-frequency base material requirements, halogen-free verification under IEC 61249-2-21, RoHS Directive 2011/65/EU Annex II, and REACH Regulation (EC) No 1907/2006. The downstream production process blends the hydrocarbon resin with a PPE/TAIC thermoset and 50–70 wt% spherical silica filler under vacuum high shear at 1,500–2,500 rpm to prevent air entrapment; the varnish is then coated onto 1078 or 2116 E-glass. Prepreg manufacturing on a clean-room horizontal treater uses beta-ray thickness gauges and inline basis-weight control, holding resin content at 50–65%. Lamination is carried out in a vacuum press at 200–220 °C and 3.0–4.0 MPa with a staged pressure ramp beginning after the resin reaches 120 °C. The terminal product is a panel-level antenna board or power amplifier carrier for 32TR/64TR massive MIMO radios.
For 77 GHz automotive radar antenna boards, the resin system must balance low transmission loss with CAF resistance through 1,000 h at 85 °C/85% RH and 50 V bias. The M6-M8 hydrocarbon resin is introduced at 12–20 wt% of the organic resin fraction; loadings above 20 wt% reduce polar adhesion to copper and can lower copper peel strength below the 0.8 N/mm threshold after thermal stress, as measured by IPC-TM-650 2.4.8. The qualification path uses IPC-4101E high-frequency rigid laminate requirements, UL 94 V-0, and production controls under IATF 16949; restricted substances are verified against RoHS Directive 2011/65/EU Annex II. Downstream, the PCB fabricator laser-drills vias through 0.10–0.15 mm cores, plasma-desmears with a CF4/O2 mixture, seeds electroless copper, and patterns 50–75 µm line/space traces by semi-additive processing. The laminate is processed into a 3–6 layer radar antenna board with a finished thickness of 0.3–0.8 mm; the dielectric constant is maintained at 3.0–3.4 at 77 GHz. Prepreg storage above 60% RH requires pre-drying at 60 °C for 24 h before lamination to prevent microvoid formation at the copper-resin interface. The terminal product is the antenna substrate within a 77–81 GHz automotive long-range radar sensor.
Unlike discrete prepreg lamination, sequential build-up films for high-density IC test boards require the lowest possible dissipation factor at 25–40 GHz without sacrificing laser via processability. In this configuration the M6-M8 hydrocarbon resin is limited to 8–15 wt% of the organic film solids; above 15 wt%, the cured film becomes brittle and 50 µm microvia sidewall cracking appears after thermal stress, while below 8 wt% the dielectric loss target becomes difficult to hold. The film is produced by slot-die coating a 20–35 µm resin layer onto a 50 µm PET carrier; coating viscosity is held at 1,000–3,000 mPa·s at 25 °C, and a 3-zone convection oven at 80–120 °C reduces residual solvent to below 0.5%. The specification path combines IPC-4101E for the core, IPC-6012 Class 3 for the finished board, and UL 94 VTM-0 for the thin film. Published data for this specific configuration is limited; film formulators running qualification panels should verify gel time and UV laser energy thresholds on production-scale equipment. Fabricators laminate the film at 120–150 °C and 0.8–1.2 MPa under vacuum, then form 30–50 µm microvias with a 355 nm UV laser; plasma desmear removes 2–5 µm of resin before electroless copper deposition. The terminal product is a high-density IC test board or optical transceiver substrate supporting 112 Gbps PAM4 signaling.
Independent of terrestrial data-center qualification, space-grade high-speed interconnect panels add outgassing and thermal-cycling acceptance gates that constrain the M6-M8 hydrocarbon resin loading. The addition is restricted to 5–12 wt% of the resin system because higher loadings can raise total mass loss and collected volatile condensable material beyond the limits of ASTM E595-15; acceptance is typically TML ≤ 1.0% and CVCM ≤ 0.10%. The cured resin system is also subjected to 500–1,000 thermal cycles from −55 °C to 125 °C under IEC 60068-2-14 Test Na; microcrack acceptance is verified by microsection after thermal stress. The low-polarity hydrocarbon phase reduces moisture-induced swelling but must be crosslinked sufficiently to suppress outgassing species; volatile removal is performed by a post-cure vacuum bake at 150–180 °C for 4–6 h. Compliance references include IPC-4101E for base materials, ECSS-Q-ST-70-71 for material selection in space applications, and RoHS Directive 2011/65/EU Annex II. Lamination is conducted in a clean autoclave at 180–200 °C and 2.5–3.5 MPa, with prepreg stored below 5 °C and conditioned before layup to avoid blocking. The terminal product is a multi-layer high-speed backplane or phased-array feed board operating in low-Earth orbit or geosynchronous payloads.
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In high-speed copper-clad laminate compounding, the binder resin governs dielectric loss, moisture uptake after reflow, and dimensional stability of thin core constructions. Sunmun Technology M6-M8 Hydrocarbon Resin is positioned as a low-polarity, crosslinkable hydrocarbon modifier for halogen-free CCL varnishes used in network switch, server, and automotive radar substrates. The product is supplied in two grades differentiated primarily by molecular weight and melt flow characteristics. M6 has a nominal softening point of 115–125°C and a melt viscosity at 150°C of approximately 0.8–1.5 Pa·s, measured by ASTM D3236 cone-plate viscometry. M8 has a nominal softening point of 125–135°C and a melt viscosity at 150°C of approximately 2.0–3.5 Pa·s. Both grades are soluble in MEK/toluene blends and can be compounded at hydrocarbon resin loadings of 10–40 phr with polyphenylene ether, triallyl isocyanurate, or styrene-maleic anhydride co-binders. The resin backbone contains low concentrations of polar ester and hydroxyl groups; cured plaques exhibit moisture absorption below 0.12 wt% under IPC-TM-650 2.6.2.1 and dielectric dissipation factor below 0.0030 at 10 GHz using IPC-TM-650 2.5.5.9. These values are representative of the product datasheet and should be verified against lot-specific certificates of analysis before use in qualification builds.
| Property | M6 | M8 | Test Method |
|---|---|---|---|
| Softening point | 115–125°C | 125–135°C | ASTM E28 |
| Melt viscosity at 150°C | 0.8–1.5 Pa·s | 2.0–3.5 Pa·s | ASTM D3236 |
| Dk at 10 GHz cured plaque | 2.60–2.70 | 2.55–2.65 | IPC-TM-650 2.5.5.9 |
| Df at 10 GHz cured plaque | 0.0020–0.0030 | 0.0018–0.0026 | IPC-TM-650 2.5.5.9 |
| Moisture absorption | <0.12 wt% | <0.10 wt% | IPC-TM-650 2.6.2.1 |
Dielectric and thermal benchmarks are normally performed on cured plaques, not on neat resin film. The representative values above are observed in a 30 phr M6-M8 / 25 phr PPE / 35 wt% fused silica formulation after lamination at 190°C for 90 min. Relative permittivity and dissipation factor are sensitive to filler morphology, glass weave volume fraction, and copper surface treatment; the resin contribution should therefore be extracted from final laminate data rather than neat resin slabs.
Conventional dicyclopentadiene resins provide low dielectric constant but often carry high exothermic cure and narrow B-stage windows. Polyphenylene ether resins deliver excellent dielectric stability but require higher melt processing temperatures and can produce high-viscosity varnishes at practical solids contents. Sunmun M6-M8 resins are formulated to operate between these two profiles: they retain the low Dk of DCPD systems while reducing the cure exotherm and increasing filler wet-out through lower melt viscosity. In a hydrocarbon/PPE blend at 30 wt% PPE replacement with M8, the Brookfield varnish viscosity at 25°C was reduced by approximately 20–30% relative to a 100% DCPD control at equivalent 55 wt% solids in toluene/MEK. The resulting prepreg exhibited a gel time of 220–260 s at 170°C by IPC-TM-650 2.3.18, compared with 180–210 s for the DCPD control. This broader gel window supports stable B-staging on horizontal treaters running above 4 m/min.
Against PPE-only formulations, the hydrocarbon resin reduces compound viscosity and allows filler loadings in the dielectric layer to reach 35–45 wt% without exceeding a varnish viscosity of 600 mPa·s at 25°C. The M6-M8 resins also contain controlled vinyl functionality for co-curing with PPE chain ends, which reduces phase separation after lamination. DMA traces from cured films show a single tan δ peak between 180–220°C, indicating compatibility at the 10–40 phr loading window. By contrast, unmodified C₉ aromatic resins in the same blend produced secondary tan δ shoulders above 0.10 and increased Z-axis CTE.
For varnish compounding, M6-M8 is typically dissolved at 50–60 wt% solids in a 70/30 w/w toluene/MEK mixture using a jacketed high-shear disperser. Addition of the initiator should follow full resin dissolution to avoid localized exotherm. In pilot runs on a 300 mm-wide horizontal treater with two drying zones, varnish prepared with M8 exhibited stable resin pickup of 38–42 wt% on 2116 E-glass at 5 m/min. Dry-edge powdering was not observed when the first zone temperature remained below 110°C and the second zone below 160°C. B-stage volatiles were held at 0.4–0.8 wt% using IPC-TM-650 2.3.16. These processing conditions are recommended as starting points; exact settings depend on treater airflow and resin bath turnover.
Filler dispersion was checked on a 50 L planetary mixer running at 35 rpm. Fused silica with median particle size 2.0 µm was added incrementally over 30 min. After 60 min of mixing, the Hegman grind exceeded 7 under ASTM D1210, and no hard agglomerates above 20 µm were observed by optical microscopy. Over-mixing beyond 90 min increased varnish temperature to 38°C and initiated a 5–8% viscosity rise due to partial olefin reaction at the initiator surface, confirming that high-shear dispersion must be time-limited when initiator is present. In separate runs using a 400 mm-wide coater with air flotation drying, resin bath viscosity drifted upward by 10–15% over 8 h due to solvent evaporation from the open bath. Maintaining a solvent feed of 0.5–1.0 wt% of bath mass per hour controlled drift without affecting flammability limits.
Grade selection between M6 and M8 is governed by prepreg flow and lamination fill requirements. M8 with its higher melt viscosity is preferred for high-layer-count backplanes and thick copper features where excessive resin flow causes starvation at board edges and in via fields. In press simulation using a 20 mm diameter parallel-plate rheometer, M8 maintained a minimum complex viscosity of 1,200 Pa·s during cure at 190°C, whereas M6 fell below 600 Pa·s. This difference translates to less squeeze-out in 28-layer books. M6 is used in thin-core or low-flow designs where high resin mobility is required to wet weave and avoid microvoids. Lamination of M6-based prepregs at 190°C and 2.5 MPa for 90 min over 18 µm reverse-treated foil produced void-free fill at 60 vol% resin content, verified by optical microsection per IPC-A-600J.
For laser-drilled via structures, M6 exhibits better conformability in 40–60 µm dielectric layers at 1.8–2.0 MPa pressure. Excessive resin flow with M6 is managed by adding 0.5–1.0 phr of a high-molecular-weight styrenic block copolymer; this adjusts the resin flow window without shifting the dielectric loss beyond 0.0028. Published data for the specific viscosity response of M6-M8 in high-yield via-fill under CO₂ laser drilling are limited, but cross-section data from 150 µm through-holes indicate acceptable fill when the B-stage conversion remains below 12%.
Dielectric performance is screened on cured plaques rather than liquid resin. At 10 GHz, M6-M8 formulations with 35 wt% fused silica and 25 phr PPE typically register relative permittivity of 3.2–3.5 and dissipation factor of 0.0020–0.0028 under IPC-TM-650 2.5.5.9. At 28 GHz, split-post resonator measurements show Df values shifting upward by 0.0005–0.0010, but the resin remains within the typical screening limit of 0.0030 for high-speed digital laminates. This frequency-dependent loss behavior should be verified on final laminate thickness and copper roughness, because conductor effects become dominant at 28 GHz and above. Published data for this specific resin at 77 GHz automotive radar frequencies are limited; evaluation on 100 µm cores indicates that the dielectric loss contribution of the resin remains secondary to copper roughness, but full resonator data are required before radar qualification.
B-staging of M6-M8 varnishes requires control of residual solvent and partial conversion. Differential scanning calorimetry by IPC-TM-650 2.4.25 shows onset of cure at 150–160°C and peak exotherm at 180–195°C for M8 with 1.0 phr dicumyl peroxide. The processing window is narrower than epoxy systems; holding prepreg at 130°C for more than 5 min before final lamination advances cure beyond 15% and reduces resin flow. On transfer from the treater, B-staged prepreg should be stored at 23±2°C and <40% RH in sealed polyethylene film. Storage at 65% RH increases prepreg moisture uptake by 0.15 wt% within 24 h, and lamination of such prepreg creates microvoids after solder shock at 288°C for 30 s per IPC-TM-650 2.6.8. Cold storage at 4°C is used for durations beyond 30 days.
Lamination press cycle for a 0.75 mm, 8-layer construction using M8 and 35 µm HVLP copper starts with vacuum below 5 kPa, heated from 40°C to 190°C at 3°C/min, with a 15-min soak at 110°C to remove residual moisture. Curing is performed at 190°C and 2.4–2.8 MPa for 90–120 min. Pressure should be applied after the charge reaches 140°C to prevent early resin gelation before air evacuation. Post-lamination bake at 220°C for 2 h improves chemical resistance and dimensional stability, increasing Tg by 5–10°C.
In high-layer-count lamination, the press cycle must also account for intra-book temperature lag. Thermocouple data from a 24-layer book of 0.6 mm core and 106 prepreg showed center-layer lag of 8–12°C behind the platen setpoint during the 3°C/min ramp. Extending the final cure soak to 120 min is therefore required to ensure the core of the book reaches at least 185°C for 60 min. Inadequate center-layer cure is detectable as low Tg by IPC-TM-650 2.4.25 and as increased desmear attack after permanganate processing.
M6-M8 is halogen-free by formulation and is tested against the bromine and chlorine limits of IEC 61249-2-21. The resin does not contain polybrominated biphenyls or diphenyl ethers. A compliance matrix is provided below; batch-specific declarations are required for each production lot.
| Requirement | Method/Standard | Criterion |
|---|---|---|
| RoHS restricted substances | 2011/65/EU Annex II | Below maximum concentration values |
| REACH SVHC | EC 1907/2006 | <0.1 wt% |
| Halogen content | IEC 61249-2-21 | Br <900 ppm, Cl <900 ppm, total <1500 ppm |
| Thermal decomposition | IPC-TM-650 2.4.24.6 | Td5% > 400°C |
| Glass transition | IPC-TM-650 2.4.25 | Tg 180–220°C |
Operational boundaries for these resins include high-shear mixing below 40°C during varnish preparation and avoidance of amine-based curing agents, which cause premature crosslinking at room temperature. Unmodified M6-M8 should not be exposed to open air for more than 12 h in ambient conditions above 30°C because surface oxidation increases melt viscosity and can shift B-stage flow. The product is supplied in 25 kg bags or 500 kg supersacks with desiccated packaging; opened material should be used within 7 days or resealed under nitrogen.