| Код ТН ВЭД | 978691 |
| Dielectric Constant | 2.65 at 1 MHz |
| Dissipation Factor | 0.0008 at 1 MHz |
| Cure Temperature | 250 °C |
| Viscosity | 350–1400 mPa·s (grade dependent) |
| Refractive Index | 1.54 at 632.8 nm |
| Optical Transparency | >90% in visible/NIR range |
| Adhesion Strength | Excellent adhesion to silicon, glass, metals, and III-V compounds |
| Moisture Absorption | <0.1% after 24 h water immersion |
| Thermal Decomposition Temperature | >350 °C (5% weight loss in N2) |
| Film Thickness Range | 1–100 μm per coat |
| Resolution | 1–5 μm features in photosensitive grades |
| Residual Stress | Low stress, <30 MPa after full cure |
Как аккредитованная DSBCB бензоциклобутеновая смола для упаковки и оптоэлектроники - завод Desytek, мы соблюдаем строгие протоколы качества - каждая партия подвергается строгим испытаниям для обеспечения последовательных стандартов эффективности и безопасности.
| Упаковка | Packaged in sealed, moisture-proof containers under inert gas, available in 1 kg quantities for packaging and optoelectronic applications. |
| Погрузка контейнера (20-футовый контейнер) | 20′ FCL: one sealed container of DSBCB Benzocyclobutene Resin, safely packed in drums for packaging and optoelectronics use. |
| Доставка | DSBCB Benzocyclobutene Resin ships in sealed, light-protected containers to preserve purity and reactivity. Transport follows standard chemical safety protocols, with proper labeling and handling documentation. Keep away from moisture, heat, and ignition sources. Ensure compatible packaging and temperature-controlled conditions during transit for optoelectronic and packaging applications. |
| Хранение | Store DSBCB Benzocyclobutene Resin in its original, tightly sealed container under inert gas (nitrogen) in a cool, dry, dark environment, ideally refrigerated (2–8°C). Protect from moisture, oxygen, heat, and UV light. Avoid repeated temperature fluctuations. Keep away from ignition sources and incompatible materials. Follow manufacturer’s specific shelf-life and handling guidelines. |
| Срок годности | Shelf life is typically 6 months when stored sealed below 10°C, protected from light and moisture. |
Конкурентоспособные бензоциклобутеновые смолы DSBCB для упаковки и оптоэлектроники - цены Desytek, которые соответствуют вашему бюджету - гибкие условия и индивидуальные котировки для каждого заказа.
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DSBCB Benzocyclobutene Resin for Packaging & Optoelectronics - Desytek is a spin-on and dispense thermosetting dielectric formulated from divinylsiloxane-bis-benzocyclobutene oligomers. The cure mechanism is ring-opening conversion of the benzocyclobutene group to an o-quinodimethane intermediate, followed by Diels-Alder cycloaddition. No catalyst, water, or volatile condensation by-product is released; film shrinkage is therefore lower than in condensation-cured polyimides. The cured matrix combines a crosslinked aromatic structure with siloxane segments, which lowers the dielectric constant and reduces moisture uptake. DSBCB is used as a permanent interlayer dielectric in wafer-level packaging, as a passivation and stress-buffer layer over copper redistribution traces, as a chip-to-wafer bonding adhesive, and as cladding or overcladding in planar optical waveguides. The product is supplied as a solvent-borne formulation in mesitylene with non-volatile content between 35 wt% and 46 wt%. Batch-to-batch liquid viscosity is controlled within ±5% at 25 °C using a cone-and-plate viscometer per ASTM D4287-19. Single-coat thickness after solvent removal ranges from 1 µm to 25 µm depending on formulation solids and coating speed. The cured network shows a dielectric constant of 2.65 at 1 MHz and a dissipation factor of 0.0008 at 1 MHz under ASTM D150-18. Moisture absorption after 24 h immersion at 23 °C remains below 0.2 wt% per ASTM D570-22. The glass transition temperature exceeds 350 °C, and the coefficient of linear thermal expansion below Tg is approximately 42 ppm/°C when measured by thermomechanical analysis per ASTM E831-19. These values place DSBCB below the dielectric constant of polyimide and PBO while retaining higher thermal stability than most silicone dielectrics.
Mechanical and electrical qualification of DSBCB films on silicon and glass substrates follows the test designations listed in the comparative matrix. The cured film has a tensile modulus of approximately 2.9 GPa, elongation at break of 8%, and Shore D hardness of 85 under ASTM D882-18. Volume resistivity is approximately 1 × 10¹⁹ Ω·cm after 24 h at 23 °C, and dielectric breakdown strength is approximately 3 MV/cm per ASTM D149-20. Thermal decomposition temperature in nitrogen is near 350 °C by thermogravimetric analysis at 10 °C/min per ASTM E1131-20. These properties remain stable after thermal aging at 300 °C for 100 h in nitrogen, with dielectric constant shifting less than 0.05 and dissipation factor increasing no more than 0.0005. For optoelectronic integration, the refractive index of the cured film at 850 nm is approximately 1.55; published data for DSBCB-specific values at 1550 nm are limited, but the benzocyclobutene class is reported between 1.54 and 1.56.
| Property | DSBCB | Polyimide | PBO | Silicone | Test method |
|---|---|---|---|---|---|
| Dielectric constant at 1 MHz | 2.65 | 3.2–3.5 | 2.9 | 2.7–3.2 | ASTM D150-18 |
| Dissipation factor at 1 MHz | 0.0008 | 0.002–0.010 | 0.001 | 0.001–0.010 | ASTM D150-18 |
| Moisture absorption | <0.2 wt% after 24 h | 1–3 wt% | 1.5 wt% | <0.2 wt% | ASTM D570-22 |
| CTE below Tg | 42 ppm/°C | 40–50 ppm/°C | 55 ppm/°C | 250–350 ppm/°C | ASTM E831-19 |
| Decomposition temperature in nitrogen | >330 °C | >450 °C | >450 °C | >300 °C | ASTM E1131-20 |
On production coaters, DSBCB is dispensed through a 0.1 µm point-of-use filter. Wafers are pre-cleaned and primed with a silane-coupling adhesion promoter; the promoter is spin-coated and hot-plate treated before DSBCB application. A typical film sequence includes static dispense, spin-out at 500 rpm for 5 s, final spin at 1500–3500 rpm depending on target thickness, and edge-bead removal with an approved aromatic solvent. Soft bake is performed at 100–150 °C for 90–120 s on a contact hot plate. Final cure is completed at 250 °C for 60 min in a nitrogen-purged convection oven or vertical furnace. Multi-layer stacks require a stepped ramp of 2–5 °C/min from room temperature to 250 °C to prevent skinning and solvent blistering. Coated wafers may be stored in a desiccator before cure; exposure to high humidity does not degrade the oligomer but can produce interfacial microvoids.
Single-coat DSBCB films above 25 µm often retain residual solvent and may crack during thermal cycling because the volumetric expansion mismatch between the organic layer and silicon increases with thickness. In wafer-level redistribution, the dielectric is deposited over copper traces with step heights from 5 µm to 15 µm. Overburden in the trench region remains lower than the field region, and the subsequent cure can produce thickness gradients greater than 10%. Copper trace sidewalls are particularly prone to void formation if the DSBCB layer is less than twice the metal step height. To planarize a 15 µm copper feature, a minimum dielectric thickness of 20 µm after cure is required. When total stack thickness exceeds 30 µm, residual tensile stress at room temperature may initiate cracking at the base of high-aspect-ratio vias. Two thinner coat-cure cycles are preferable to a single thick coat; however, the inter-coat interface can exhibit reduced adhesion if the first layer is overcured. Process engineers therefore set the first cure at 200 °C for 30 min, followed by a final cure at 250 °C for 60 min. Published data for DSBCB-specific critical thickness on copper redistribution with high-density via arrays is limited; the above limits are observed in pilot-scale evaluations.
Benzocyclobutene ring opening is thermally activated, but the intermediate can react with molecular oxygen instead of undergoing cycloaddition. In a nitrogen-purged oven, the oxygen concentration should be held below 100 ppm, measured by a zirconia oxygen analyzer at the exhaust. If the level rises above 100 ppm, the DSBCB film surface may remain tacky after cure, develop a yellow-brown oxidation layer, and exhibit a dissipation factor increase of 0.002 or more at 1 MHz. Oxygen-damaged films also show reduced adhesion to subsequent layers and increased dielectric constant because carbonyl and hydroperoxide species are polar and moisture-active. Production-scale failures have been documented when oven door seals degrade or when nitrogen flow is interrupted during the initial ramp from 100 °C to 200 °C. The chamber should be purged with 5–10 chamber volumes of nitrogen before wafer load, and positive pressure must be maintained throughout the cure. Rapid venting after cure can introduce oxygen while the film is still above 150 °C; wafers should be cooled to below 100 °C under nitrogen before removal. These constraints are not required for condensation-cured polyimides, which tolerate a nitrogen or vacuum environment but do not rely on oxygen-sensitive intermediates.
Relative to polyimide, DSBCB cures at 250 °C instead of 350 °C and produces lower dielectric constant and lower moisture absorption. Polyimide is typically supplied as a polyamic acid precursor, which releases water during imidization; this by-product can oxidize copper unless reducing atmosphere or careful ramp conditions are used. DSBCB releases no condensation water and can be processed directly over copper redistribution traces without desmear or post-cure reduction. Compared with PBO, DSBCB provides lower moisture uptake and a longer pot life at room temperature; PBO often requires cold storage and has a narrower post-exposure bake latitude for photosensitive grades. Compared with silicone, DSBCB has a much lower coefficient of thermal expansion and higher tensile modulus, which reduces warpage in wafer-level fan-out structures but increases the risk of cracking at high thickness. Silicone remains preferred where a low-modulus stress buffer is required over large-area passivation; DSBCB is selected where dielectric loss, planarity, and thermal stability are primary constraints. Compared with epoxy molding compounds and liquid encapsulants, DSBCB exhibits lower dielectric constant and lower ionic contamination; however, DSBCB is not a structural encapsulant and is limited to total layer thicknesses below 50 µm.
In wafer bonding applications, DSBCB is coated on the cap wafer or device wafer and partially cured to a tack-free state. The bond is formed under vacuum at 250 °C with an applied pressure of 0.1–0.3 MPa for 10–60 min. Bondline thickness after bonding is controlled by initial coating thickness and bonding pressure; high-aspect-ratio cavities require a low-viscosity formulation to avoid air entrapment. Unlike glass frit bonding, DSBCB does not require thermal budgets above 300 °C and does not generate alkali contamination.
| Parameter | Standard or regulation | Typical requirement |
|---|---|---|
| Dielectric constant | ASTM D150-18 | 2.60–2.75 at 1 MHz |
| Dissipation factor | ASTM D150-18 | <0.001 at 1 MHz |
| Moisture absorption | ASTM D570-22 | <0.2 wt% after 24 h |
| CTE below Tg | ASTM E831-19 | 40–45 ppm/°C |
| Decomposition temperature | ASTM E1131-20 | >330 °C at 10 °C/min |
| Restricted substances | RoHS 2011/65/EU Annex II | Not detected above homogeneous material limits |
DSBCB films are also used as planarizing cladding layers in polymer optical waveguides and as dielectrics in photonic packaging. The cured film exhibits low absorption across the 850–1550 nm range; propagation loss is governed primarily by sidewall roughness and particulate contamination rather than bulk absorption. A spin-coated DSBCB cladding layer reduces the step-index contrast between waveguide core and air, which lowers scattering loss at the core sidewall. In chip-scale optical interposers, the material serves as undercladding and overcladding around a higher-index core polymer; precise refractive index matching is achieved by controlling cure temperature and post-cure oxidation. Oxygen ingress during cure, as described above, shifts refractive index upward and increases optical loss in the near-infrared. For DSBCB-specific optical loss figures, published data remain limited; evaluations should include out-of-plane loss measurements at the target wavelength before design freeze.