| HS Code | 544331 |
| Dielectric Constant | 2.35 at 10 GHz |
| Dissipation Factor | 0.0012 at 10 GHz |
| Glass Transition Temperature | 185 °C |
| Thermal Decomposition Temperature | 320 °C (5% weight loss) |
| Water Absorption | 0.05% by weight (24h immersion) |
| Tensile Strength | 56 MPa |
| Elongation At Break | 4.2% |
| Adhesion Strength | 1.8 kN/m on copper foil |
| Refractive Index | 1.51 at 589 nm |
| Volume Resistivity | 1.2 × 10^16 Ω·cm |
| Chemical Resistance | Resistant to acids, alkalis, and common organic solvents |
| Coefficient Of Thermal Expansion | 38 ppm/°C |
As an accredited Next-Gen M10 Hydrocarbon Resin for 6G/AI - EM Technology factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged as 25 kg net in moisture-resistant multi-layer paper bags with PE liner, ensuring safe handling and stability. |
| Container Loading (20′ FCL) | Next-Gen M10 Hydrocarbon Resin for 6G/AI-EM Technology loaded in 20′ FCL, packed in bags on pallets, secured for safe transport. |
| Shipping | Next-Gen M10 Hydrocarbon Resin is shipped in sealed, inert-lined drums or IBCs to prevent moisture contamination. Transport under dry, temperature-controlled conditions, away from ignition sources. Standard non-hazardous chemical logistics apply, with proper labeling and handling documentation to ensure safe, compliant delivery for EM technology applications. |
| Storage | Store in a cool, dry, well-ventilated area below 40°C, away from direct sunlight, heat, open flames, and strong oxidizers. Keep containers tightly sealed to prevent moisture contamination and oxidation. Avoid prolonged exposure to air. Use proper grounding during transfer. Follow manufacturer safety guidelines; shelf life typically 12 months from production date. |
| Shelf Life | Shelf life: 24 months when stored unopened in a cool, dry area, away from heat and direct sunlight. |
In high-speed digital backplane fabrication for 224 Gbps PAM4 line cards, the resin matrix of the copper-clad laminate controls insertion loss after conductor roughness has been minimized. Next-Gen M10 Hydrocarbon Resin for 6G/AI EM Technology is melt-dispersed into a vinyl-terminated polyphenylene ether thermoset at 8–15 phr of resin solids to reduce B-stage melt viscosity and lower the concentration of polar end groups after cure. The saturated alicyclic backbone contributes a target relative permittivity of ≤3.55 and a dissipation factor of ≤0.0028 at 10 GHz when measured per IPC-TM-650 2.5.5.5 and 2.5.5.9 on a 1078 low-D glass fabric with 50 wt% resin content. A production-scale treater with 2.2 m web width and 12–18 m/min line speed impregnates the glass using a methyl ethyl ketone/toluene solution at 60:40 solvent ratio and 35–40% solids. Oven zones are set at 130 °C, 150 °C, and 170 °C; residual solvent is held below 1.5 wt% by thermogravimetric analysis because sheet-to-sheet Df deviation increases by 0.0004 when residual solvent exceeds 1.8 wt%. Glass fabric is pre-dried at 105 °C for 4 h whenever warehouse relative humidity exceeds 60%. The B-staged prepreg is laminated at 210 °C and 3.0 MPa for 120 min in an 8-opening press with platen parallelism maintained at 0.05 mm/m or better. Copper peel strength is verified at ≥0.9 N/mm using IPC-TM-650 2.4.8. Terminating the formulation at 18 phr M10 or above reduces the TMA glass transition temperature below 180 °C; below 8 phr, voiding appears around 1080 glass bundles because melt viscosity is insufficient. The cured laminate is converted into 18 µm reverse-treated copper foil and fabricated into 4-layer AI accelerator backplanes for 112/224 Gbps channels. The non-brominated system meets RoHS Directive 2011/65/EU as amended by (EU) 2015/863 for lead-free assembly at 260 °C reflow.
Insertion loss in antenna-in-package build-up films is limited less by bulk permittivity than by interfacial void density and residual polar solvent. M10 is incorporated at 5–12 wt% of total adhesive solids in an epoxy-cyanate ester blend containing 40–55 wt% cyanate ester, 20–30 wt% bisphenol A epoxy, 5–12 wt% M10, and 0.05–0.15 phr imidazole accelerator. The cured film target is a Df ≤0.003 at 10 GHz after 168 h of 85 °C/85% RH aging, measured according to IPC-TM-650 2.5.5.9. Cyanate ester cyclotrimerization conversion is held above 95% by FTIR; residual unreacted cyanate ester absorbs atmospheric moisture and shifts Df during biased humidity testing. The adhesive is slot-die coated onto 38 µm silicone-coated PET carrier film. Drying zones are set at 90 °C, 120 °C, and 130 °C. The B-stage melt viscosity measured at 120 °C with a parallel-plate rheometer must remain between 1,200 Pa·s and 2,800 Pa·s. A minimum viscosity below 1,200 Pa·s produces uncontrolled resin bleed beyond the die edge, creating air entrapment at the wafer edge; a viscosity above 2,800 Pa·s prevents the dry film from conforming to 15 µm copper pillar topography. Production lot-to-lot variation of M10 melt viscosity at 140 °C is typically ±8%, which maps to a minimum viscosity shift of approximately ±200 Pa·s in the bonding film. Vacuum lamination onto 300 mm wafers is performed at 100 °C and 0.4 MPa for 120 s, followed by cure at 180 °C for 2 h in a nitrogen-purged oven. The terminal build-up film is used in 8×8 patch array antenna-in-package modules with a total die-to-antenna spacing of 120 µm. Formulation stability requires imidazole accelerator below 0.15 phr; higher levels with M10 reduce the cured Tg below 150 °C and increase warp on 12-inch fan-out panels.
Because solvent-borne low-loss adhesives for two-layer flexible copper-clad laminates require room-temperature tack and low dynamic viscosity during roll lamination, M10 is screened as a secondary tackifier in an epoxy-acrylate adhesive at 6–10 wt% of total solids. The adhesive solids comprise 30–45 phr liquid epoxy, 10–20 phr carboxylated nitrile rubber, 6–10 phr M10, 4–6 phr dicyandiamide, 0.1–0.3 phr imidazole adduct, and 0.5 phr silane coupling agent. The formulation is coated on 35 µm rolled copper foil by reverse comma roll coating at 40–60 µm wet thickness. B-staging is carried out in a 3-zone oven from 120 °C to 150 °C; residual solvent is held below 1.2 wt%. Roll-to-roll vacuum lamination is then conducted at 160–180 °C and 1.5 MPa for 45 min with platen parallelism maintained at 0.05 mm/m. Etched-free film targets are Dk ≤3.2 and Df ≤0.003 at 10 GHz per IPC-TM-650 2.5.5.9. A M10 loading above 12 wt% causes solder dip failure at 300 °C for 60 s using IPC-TM-650 2.4.13; decomposition volatiles blister the adhesive layer between copper and polyimide substrate. The converted material is supplied as 2-layer FCCL for wearable AI edge modules and foldable antenna elements operating in the 6 GHz band.
Conductive adhesives used to bond EMI shielding enclosures in AI server modules operate near the percolation threshold of silver-coated copper flake at 72–75 wt%. M10 is introduced at 3–6 wt% of the binder fraction to lower masterbatch viscosity and allow higher flake loading without cracking during dispense through a 22-gauge needle. The binder consists of bisphenol F epoxy 15–20 wt%, M10 3–6 wt%, dicyandiamide 1.5–2.0 wt%, titanate coupling agent 0.5 wt%, and fumed silica 1–2 wt%; silver-coated copper flake forms the balance at 75–80 wt%. Mixing is performed in a planetary mixer at 500 rpm for 10 min, followed by two passes through a three-roll mill with a 25 µm rear gap and a 15 µm front gap. Cone/plate viscosity at 25 °C is controlled between 30,000 mPa·s and 60,000 mPa·s. Excessive shear beyond two passes fractures the flake and raises volume resistivity above 20 mΩ·cm; insufficient shear leaves resin-rich pockets that shift shielding effectiveness by 10 dB across the 30 MHz–1 GHz range. Cure is carried out at 120 °C for 1 h in a forced convection oven. The product is applied to EMI gasket flanges and connector frames where shielding effectiveness exceeds 80 dB at 1 GHz when tested per IEEE 299-2006. Pot life is limited to 4 h at 40 °C; continued storage doubles viscosity after 8 h at 25 °C. Primary aliphatic amine hardeners are avoided because open-time exposure above 4 h leads to phase separation between the amine-functional network and the hydrocarbon resin, causing gasket bond delamination.
Radome laminates for 28 GHz fixed wireless access must balance dielectric transparency, rain erosion resistance, and low moisture uptake. M10 is used in a cyanate ester prepreg matrix at 10–20 phr relative to 100 parts cyanate ester, with 5 parts epoxy flexibilizer and 0.1 phr manganese octoate catalyst. The prepreg is B-staged at 120 °C for 3 min to a cyanate ester conversion of approximately 20% before layup. Autoclave cure is performed at 177 °C and 0.7 MPa for 2 h; pressure application is initiated at 70 °C to prevent void growth before gelation. Water absorption after 24 h immersion is held below 0.5% per ASTM D570-22. The dielectric target for a dry coupon is Df ≤0.005 at 28 GHz using a split-post resonator per ASTM D2520. Published data for M10 in cyanate ester at 28 GHz is limited; supplier dielectric coupon data should be verified with the split-post resonator on the production laminate before lot acceptance. Each 5 phr increment of M10 reduces the dry Tg by 5–10 °C; the formulation is adjusted to keep the dry Tg above 180 °C after radome paint cure. The cured laminate is machined into a 3 mm thick radome shell for a 28 GHz base station antenna, with a painted outer surface qualified for rain erosion to 250 km/h rotating arm test conditions.
Directly beneath the redistribution layer, low-stress encapsulant materials absorb thermomechanical mismatch between a 600 mm² silicon interposer and an organic substrate. M10 is melt-blended into a phenol novolac epoxy molding compound at 2–6 wt% of total formulation. The compound contains spherical fused silica 80–88 wt%, epoxy resin 8–12 wt%, phenol hardener 2–4 wt%, carbon black 0.3 wt%, and carnauba wax 0.2 wt%. Compounding is performed on a twin-screw extruder with L/D 40:1, barrel zones 90–110 °C, screw speed 250 rpm, and pelletizing at 4 mm diameter. Transfer molding is carried out at 175 °C and 6.9 MPa for 120 s, followed by post-mold cure at 175 °C for 4 h. The molding compound exhibits a CTE α1 below 12 ppm/°C per ASTM E831, flexural modulus above 15 GPa per ASTM D790, and UL 94 V-0 at 0.8 mm thickness. M10 levels above 6 wt% raise CTE above 12 ppm/°C and reduce the TMA glass transition below 150 °C; package warpage at room temperature increases to more than 250 µm for a 20 × 20 mm fan-out wafer-level package. The encapsulant is qualified for AI accelerator packages with JEDEC MSL 2 and 220 °C reflow peak temperature.
| Application sector | Primary standard | Test condition | Acceptance window |
|---|---|---|---|
| High-speed CCL | IPC-TM-650 2.5.5.9 | 10 GHz after 24 h at 23 °C/50% RH | Df ≤0.0028 |
| AiP bonding film | IPC-TM-650 2.5.5.9 | 10 GHz after 168 h at 85 °C/85% RH | Df ≤0.003 |
| Flexible CCL | IPC-TM-650 2.5.5.9 | 10 GHz etched-free film | Df ≤0.003 |
| EMI conductive adhesive | IEEE 299-2006 | 30 MHz–1 GHz | Shielding effectiveness ≥80 dB |
| Radome laminate | ASTM D2520 | 28 GHz dry coupon | Df ≤0.005 |
| Fan-out encapsulant | UL 94 / ASTM E831 | 0.8 mm thickness / CTE α1 | V-0 / ≤12 ppm/°C |
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Next-Gen M10 Hydrocarbon Resin for 6G/AI - EM Technology is a low-polarity hydrocarbon binder developed for copper-clad laminates, high-speed prepregs, and electromagnetic-compatible substrates operating beyond 10 GHz. The product is supplied as a pale, solvent-soluble resin; its release profile is controlled against ISO 4625-1:2020 for softening point, ISO 1133-1:2022 for melt flow, ASTM D6604-00(2017) for glass transition, and ASTM D1544 for color. M10 is positioned for mixed-signal boards where insertion-loss budgets require low dielectric loss and stable dielectric constant after moisture conditioning. Because M10-specific data at frequencies above 40 GHz is limited, the following sections distinguish between published resin-class ranges and the lot-specific values that must be confirmed by certificate of analysis.
The resin is intended as a formulation component rather than a standalone dielectric. In filled systems, M10 is combined with fused silica, boron nitride, or proprietary low-Dk fillers to achieve a target dielectric constant below 2.6 at 10 GHz when measured by IPC-TM-650 2.5.5.13. The manufacturing specification is written around lot-to-lot consistency in molecular weight distribution and 150 °C melt viscosity rather than a single resin purity value. Storage and handling conditions are part of the specification: exposure to ambient air above 60 % RH is controlled by resealable foil-lined packaging, and pre-drying is recommended before melt compounding. This distinction matters because hydrocarbon resins of this class can retain moisture at polar ester or acid impurities; the non-polar backbone alone does not guarantee low moisture uptake unless residual functional groups are held to controlled limits.
For 6G/AI architectures, the substrate must preserve signal integrity through differential pairs, backplane vias, and antenna-feeding structures. Hydrocarbon resin binders with low aromaticity reduce electronic polarization and moisture sorption, both of which contribute to dielectric loss. In contrast, a conventional high-aromatic C9 tackifier may exhibit dielectric constant values in the 2.6 to 2.8 range and loss tangent values above 0.003 at 10 GHz, limiting its use in long-reach channels. M10 is formulated to shift the resin-base loss envelope toward values more compatible with 28 GHz and 39 GHz millimeter-wave bands, although final laminate loss is dominated by copper foil roughness, glass fabric type, and filler content.
Process selection data for M10 trials have been collected on production-scale co-rotating twin-screw extruders with L/D 44:1. Barrel setpoints from 180 °C to 220 °C are used for filler masterbatches. At screw speeds above 600 rpm, melt temperature excursions above 250 °C are observed when silica loading exceeds 60 wt%. This is a critical threshold because thermally oxidized hydrocarbon fractions raise melt viscosity and can increase high-frequency loss after lamination. Operators control specific energy input rather than barrel temperature alone; the recorded specific mechanical energy for a 50 wt% silica system is typically held between 0.25 kWh/kg and 0.35 kWh/kg depending on screw configuration and feed rate. Side-stuffing of filler after the primary melting zone reduces motor amperage spikes on twin-screw lines, but it also shortens filler wetting time; the resulting dispersion quality is verified by optical microscopy on pressed films at 50× magnification.
For prepreg varnishing, M10 is often dissolved in a mixed solvent system of cyclohexane and xylene at 25 wt% to 35 wt% solids. The varnish viscosity is adjusted to 100 cP to 250 cP at 25 °C for uniform glass-cloth impregnation on vertical treaters. A key processing limitation is solvent polarity: highly polar solvents such as N-methyl-2-pyrrolidone should be avoided because resin precipitation can occur, and amine-based hardeners or accelerators should not be added to M10-containing varnishes without compatibility testing. The non-polar hydrocarbon phase can separate from amine-cured epoxy domains, producing microvoids that degrade peel strength and increase insertion loss. On a vertical treater, the practical processing window is bounded on one side by resin pickup and on the other by residual solvent retention; air velocity and zone temperatures above 160 °C reduce residual solvent but can oxidize the resin surface if oxygen concentration is not controlled.
Three property differences are material to mmWave laminate design. First, M10 is controlled for a lower residual volatile fraction than standard C5/C9 tackifiers; the supplier’s internal release uses gravimetric loss after 24 h at 105 °C, with the acceptance window set to exclude high-boiling dimer fractions that can volatilize during lamination at 200 °C and create voids. Second, the molecular weight distribution is narrow, which reduces the high-molecular-weight tail that raises melt viscosity in pressed cores. Third, the resin is evaluated for moisture uptake after 85 °C and 85 % RH conditioning; published data for low-loss hydrocarbon resin classes show mass gain below 0.3 % after 168 h, while high-polarity epoxy systems may exceed 1.0 % under the same conditions.
In comparative form, the differentiation can be summarised as a resin-class selection issue rather than a single-value improvement. M10’s target window places it among low-loss hydrocarbon binders that must be evaluated with the same filler and glass system; changing the resin alone without adjusting silane treatment and copper type can produce no statistically significant insertion-loss improvement. Published data for this specific configuration is limited outside full laminate qualifications.
| Resin class | Dk at 10 GHz | Df at 10 GHz | Moisture uptake | Processability boundary |
|---|---|---|---|---|
| C9 aromatic hydrocarbon resin | 2.6–2.8 | 0.003–0.006 | 0.1 %–0.3 % | High aromaticity; higher Df in mmWave bands |
| DCPD resin | 2.4–2.6 | 0.0015–0.0030 | 0.1 %–0.2 % | Higher melt viscosity; requires high lamination temperature |
| Epoxy resin system | 3.0–3.8 | 0.020–0.030 at 1 MHz | 0.5 %–1.5 % | High adhesion but higher loss and moisture sensitivity |
| M10 target class | target below 2.5 | target below 0.003 | target below 0.2 % | Narrow processing window above 60 wt% filler |
Values in the table are representative literature ranges for resin classes, not M10 lot-specific certification data. M10-specific dielectric values at 28 GHz and 100 GHz require coupon testing because copper-foil roughness and glass-fabric resonance interact with resin loss.
In addition to laminate binders, M10 is evaluated in high-frequency coverlay adhesives and flexible bonding layers for multilayer constructions. In these applications, the resin is compounded with styrenic block copolymers or hydrogenated tackifiers at 15 wt% to 30 wt% to adjust peel adhesion and moisture resistance. The adhesion to polyimide and treated copper requires silane-functional promoters; without them, peel strength after 85 °C/85 % RH aging can fall below 0.8 N/mm for 25 µm thick films. This is an operational boundary because higher resin addition reduces melt viscosity and improves flow but may inhibit reflow soldering temperature resistance if the softening point is below 120 °C.
The surface chemistry of fillers and glass fabric affects M10 more than a polar epoxy system because the non-polar resin does not wet silanol groups well. In production, glass fabric is treated with silane coupling agents selected for hydrocarbon compatibility; the treatment level is monitored by X-ray fluorescence or contact-angle goniometry. If silane treatment drifts across fabric lots, the resin-rich areas can lower peel strength and create discontinuous wetting that appears as microvoids in cross-sections. This batch-to-batch interaction is among the most frequently reported production issues on vertical treaters processing M10-containing varnishes. A control limit of ±5° water contact angle on treated glass coupons is used in some facilities, but the limit depends on fabric finish and supplier.
Flame-retardant synergy in M10-based laminates follows the same dielectric penalty pattern observed across low-loss thermosets: phosphorus-based flame retardants increase formulation polarity and may raise loss tangent if the addition level exceeds the minimum needed for the chosen glass style and copper weight. In qualification trials, phosphinate-based additives above 25 wt% have shown measurable Df increase after 85 °C/85 % RH aging, making filler selection and coupling-agent choice more important than simple resin loading. M10 is not itself a UL 94-rated compound; the final laminate must be tested as an assembly, typically using the 0.254 mm to 0.508 mm core thickness range and specified copper foil. Suppliers of glass fabric and FR packages should provide lot-specific data for the complete construction.
At 28 GHz, insertion loss measurements on microstrip coupons often mask resin differences because conductor loss from untreated or high-profile copper can exceed dielectric loss. A design of experiments that fixes copper type, silane treatment, and press cycle is required before assigning loss improvements to M10. Published data for this specific configuration is limited when the test is not normalised to the same laminate resin-content and glass style. In addition, the halogen-free requirement should be verified on the finished laminate according to IEC 61249-2-21:2003 because inorganic fillers can dilute halogen content below reporting thresholds in neat resin screens.
The rheological response of M10 is measured by parallel-plate oscillatory rheometry using 25 mm plates, 1 mm gap, and a frequency sweep from 0.1 rad/s to 100 rad/s at 180 °C and 200 °C. The complex viscosity at 10 rad/s and 180 °C is more relevant to lamination flow than melt flow rate because hydrocarbon resin flow in filled prepregs occurs under low shear and non-isothermal conditions. M10 is controlled to a narrow molecular weight distribution; the supplier’s certificate reports weight-average to number-average molecular weight ratio, with typical high-frequency hydrocarbon resins in the range 1.5 to 2.0. A high-molecular-weight tail above 5000 g/mol is undesirable because it reduces wetting of glass fiber bundles and can increase resin-rich area thickness variation in multilayer boards.
Thermal gravimetric analysis of M10 by ISO 11358-1 under nitrogen shows that thermal degradation onset is not a single sharp value but a function of heating rate. For hydrocarbon resins of this class, the supplier recommends defining the process limit as the temperature at which 2 % mass loss occurs, rather than the extrapolated onset temperature. At 10 °C/min heating rate, this value generally exceeds 280 °C for hydrogenated hydrocarbon resins. However, oxidation during open-air drying can lower the practical ceiling; pre-drying at 80 °C for 4 h in a desiccant dryer with dew point below −40 °C is required when storage has exceeded 60 % RH. Because M10-specific published data for long-term aging under nitrogen at 150 °C is limited, the resin is qualified on final laminate properties after solder float and thermal cycling rather than on neat resin alone.
In press lamination, the melt-flow window is defined by a combination of resin melt viscosity and filler network formation. A typical press profile for M10-based cores heats from 80 °C to 210 °C at 3 °C/min, holds at 210 °C for 120 min, and cools under pressure at 1.5 MPa to avoid delamination at the copper-resin interface. The flow length measured on a spiral-flow test at 180 °C is not used as a release criterion unless the test mold geometry and filler loading are specified; otherwise, resin-rich thickness variation in the board cross-section is the controlling quality metric.
For compliance documentation, M10 is supplied with a declaration that addresses EU RoHS Directive 2011/65/EU Annex II restrictions and the REACH candidate list. Halogen testing is conducted on the resin extract rather than the final laminate because inorganic filler and glass can dilute halogens below typical reporting limits. The following table identifies the controlling methods used in technical documentation.
| Property | Method | Condition | Documentation status |
|---|---|---|---|
| Softening point | ISO 4625-1:2020 | Ring-and-ball, glycerol bath | Lot certificate |
| Melt viscosity | ISO 1133-1:2022 | Specified temperature/load by supplier | Lot certificate |
| Glass transition | ASTM D6604-00(2017) | DSC, second heat | Lot certificate |
| Dielectric constant / loss | IPC-TM-650 2.5.5.13 | 10 GHz split-post; 23 GHz optional | Qualification report on final laminate |
| Halogen content | IEC 61249-2-21:2003 | Burn and ion chromatography | Supplier declaration |
| RoHS restricted heavy metals | IEC 62321-5:2013 | Microwave digestion, ICP-OES | Supplier declaration |
Qualification of M10 for a 6G phased-array board typically involves 0.254 mm and 0.508 mm cores, 35 µm and 18 µm low-profile copper, and thermal shock conditioning from −55 °C to 125 °C for 500 cycles in accordance with IPC-TM-650 2.6.7.1. Acceptance criteria for dielectric loss drift are set at 0.001 or less from the initial 10 GHz measurement. Because published data for M10 at 100 GHz is limited, early adopting fabricators evaluate coupons on the actual board stackup rather than relying on neat resin data. The product enters a qualified bill of materials only after resin-content tolerance is held within ±2 % by weight across a continuous prepreg lot. In high-speed backplane applications, the more stringent requirement is not the neat resin loss tangent but the repeatability of the cured laminate across moisture cycling from 23 °C/50 % RH to 85 °C/85 % RH; that repeatability is the controlling qualification metric for M10-containing constructions.