Vinyl Terminated Silicone Oil RH-Vi1324

    • Product Name: Vinyl Terminated Silicone Oil RH-Vi1324
    • Factroy Site: No. 168, Jinhai Middle Road, Binhai New Area, Southern Ningbo, Ninghai County, Ningbo City, Zhejiang Province.
    • Price Inquiry: sales8@bouling-chem.com
    • Manufacturer: Zhejiang Runhe Chemical New Material Co., Ltd.
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    Specifications
    HS Code 824280
    Product Name Vinyl Terminated Silicone Oil RH-Vi1324
    Chemical Type Vinyl-terminated polydimethylsiloxane
    Cas Number 68083-19-2
    Appearance Colorless transparent liquid
    Viscosity At 25 C 1,000–5,000 mPa·s
    Vinyl Content 0.40–0.50 wt%
    Density At 25 C 0.96–0.98 g/cm³
    Refractive Index At 25 C 1.403–1.406
    Volatile Content ≤2.0 wt%
    Flash Point >100 °C
    Terminal Group Vinyl
    Storage Temperature 5–30 °C
    Shelf Life 12 months

    As an accredited Vinyl Terminated Silicone Oil RH-Vi1324 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 200 kg steel drums with removable lids and internal liners, suitable for industrial handling and storage.
    Container Loading (20′ FCL) 20′ FCL container loaded with Vinyl Terminated Silicone Oil RH-Vi1324 in properly sealed drums, secured, labeled, and documented for safe shipment.
    Shipping Vinyl Terminated Silicone Oil RH-Vi1324 is typically shipped in sealed steel drums or IBCs under ambient conditions. Keep containers dry, closed, and protected from extreme heat or contamination. It is generally not classified as dangerous goods; follow the SDS and local transport regulations.
    Storage Store in a cool, dry, well-ventilated area away from heat, sparks, open flames, and strong oxidizing agents. Keep container tightly closed when not in use to prevent contamination and moisture ingress. Protect from direct sunlight. Store at moderate ambient temperature; avoid extreme temperatures. Use compatible containers, ground/bond during transfer, follow local regulations, and maintain clear labeling and inventory.
    Shelf Life Shelf life is 12 months when kept in original, unopened packaging, dry, away from light, at room temperature.
    Application of Vinyl Terminated Silicone Oil RH-Vi1324

    In liquid silicone rubber injection moulding, RH-Vi1324 is proportioned into a two-component platinum-catalysed formulation as the vinyl-functional polysiloxane. The Part A stream contains the vinyl polymer, a polymethylhydrogensiloxane crosslinker, and fumed silica; Part B contains the vinyl polymer, platinum-divinyltetramethyldisiloxane complex at 5–10 ppm Pt, and 1-ethynyl-1-cyclohexanol as the pot-life inhibitor. Metering of the two streams at a fixed 1:1 ratio is carried out by a gear pump, followed by static mixing with 8–12 elements. The blend is cooled to 18–25°C before injection to suppress premature gelation. On a 1,600 kN clamp-force injection moulding press, the shot is injected into a closed tool at 150–190°C; cure time is adjusted from 30 s to 90 s depending on wall thickness. The Si-H:Si-Vi ratio is held between 1.2:1 and 1.8:1. Ratios below 1.0:1 produce surface tack and low crosslink density, while ratios above 2.0:1 cause hydrogen evolution, gas entrapment, and premature embrittlement. The cured material is evaluated by ASTM D2240 for durometer, ISO 37:2017 for tensile strength and elongation, and ISO 815-1:2019 for compression set after 22 h at 175°C. For a 40 Shore A moulding composition, tensile strength typically falls between 7.0 MPa and 10.0 MPa, elongation at break between 400% and 700%, and compression set from 15% to 30% without post-cure. Process drift is observed on high-speed moulding lines when the Pt concentration is reduced below 3 ppm to extend pot life; mould release force then rises and surface cure becomes sensitive to ambient sulphur contamination. The terminal articles are infant-care nipple hoods, pump diaphragms, and electrical connector seals.

    Representative screening data for a 40 Shore A addition-cure LSR based on RH-Vi1324 at varied Si-H:Si-Vi ratios
    Si-H:Si-Vi molar ratioTensile strength under ISO 37:2017Elongation under ISO 37:2017Compression set under ISO 815-1:2019Durometer under ASTM D2240
    1.0:14.5 MPa550%35%35 Shore A
    1.3:17.0 MPa600%25%38 Shore A
    1.5:18.5 MPa550%20%41 Shore A
    1.8:19.0 MPa480%18%43 Shore A
    2.0:18.0 MPa380%16%46 Shore A

    What Limits the Si-H:Si-Vi Ratio in Platinum-Catalysed Release Coatings?

    Solventless silicone release coating systems are formulated with RH-Vi1324 as the vinyl donor to control crosslink density and release force. The coating bath is prepared by blending the vinyl silicone oil with a polymethylhydrogensiloxane crosslinker to an Si-H:Si-Vi ratio of 1.4:1 to 1.8:1, a platinum catalyst concentration of 30–100 ppm Pt, and a vinyl-functional MQ resin when tighter release is required. The mixture is applied by five-roll offset coating at 0.8–1.2 g/m² to polyester or glassine substrates. Thermal cure in an air flotation oven at 120–160°C with dwell times of 5–15 s produces a crosslinked film without solvent. Crosslinker starvation below 1.2:1 leaves unreacted vinyl species that migrate into acrylic or rubber pressure-sensitive adhesives and lower peel strength after lamination. Crosslinker excess above 2.0:1 generates residual Si-H groups that undergo secondary reactions with ambient moisture, raising release force over time. Release performance is tested using FINAT FTM 3 on a tensile tester at 180° peel angle and 300 mm/min; controlled addition of MQ resin shifts release from 5–10 cN/25 mm low-force release to 30–60 cN/25 mm tight release. The terminal product is a release liner for pressure-sensitive label stock, single-sided industrial tapes, and medical adhesive carriers.

    Encapsulation of insulated-gate bipolar transistor modules and power converters with silicone gels uses RH-Vi1324 in a two-part addition-cure system where pot life and dielectric performance are coupled to the vinyl-hydride ratio. The A component is a blend of RH-Vi1324, a hydride crosslinker, and an alkynol inhibitor; the B component contains the same vinyl polymer and a platinum-cyclovinylmethylsiloxane complex at 5–20 ppm Pt. The components are metered at 1:1, mixed under vacuum at 30–50 mbar, and dispensed into the module housing at 50–80°C to lower viscosity. Cure is carried out at 80–120°C for 30–60 min. The Si-H:Si-Vi ratio is set at 1.5:1 to 2.0:1 to balance softness and extractables. The mixed viscosity is adjusted to 500–1,000 mPa·s at 25°C. The cured gel hardness is checked with a 1/4-scale cone penetrometer per ASTM D1403, with penetration values typically 6.0–8.5 mm. Dielectric strength is tested according to IEC 60243-1 on 2 mm sheets, with typical values 14–18 kV/mm before thermal ageing. Pot life at 25°C is extended to 4–8 h by adjusting inhibitor concentration, but adding more than 0.05 wt% of 1-ethynyl-1-cyclohexanol retards cure below 100°C and raises the coefficient of thermal expansion after gelation. Fumed silica is added at 0.5–2.0 wt% when thixotropic dispensing is needed; above 3.0 wt% filler the gel loses transparency and trapped bubbles become difficult to remove under vacuum. Fumed silica should be pre-dried at 120°C for 2 h when ambient relative humidity exceeds 60%. The encapsulant must be stored and dispensed away from amine-cured epoxy surfaces, sulphur-vulcanized rubber gaskets, and metal soaps, which poison the platinum catalyst. The terminal use is an optically clear stress-relief layer for wire-bonded power modules and automotive motor-drive electronics.

    HTV Extrusion Lines Running RH-Vi1324-Modified Silicone Compounds

    High-consistency silicone rubber compounds for extruded profiles and automotive coolant seals are prepared with RH-Vi1324 as a reactive processing fluid to lower compound viscosity and adjust crosslink density. On a two-roll mill at 35–45°C, 100 phr high-consistency vinyl-terminated silicone gum is blended with 20–40 phr fumed silica, 3–6 phr precipitated calcium carbonate, and RH-Vi1324 at 5–15 phr. The addition-cure package includes a methylhydrogenpolysiloxane crosslinker at an Si-H:Si-Vi ratio of 1.3:1 to 1.6:1 and a platinum-alkenyl complex at 0.5–1.0 ppm Pt. The compound is fed through a cold-feed extruder with L/D 24:1 and a barrel temperature profile from 20°C at the feed zone to 40°C at the head, then through a salt-bath or hot-air tunnel at 250–400°C for 20–60 s. Crosslink density is increased by post-curing at 200°C for 4 h to remove volatile by-products. Hardness is controlled by the ratio of RH-Vi1324 to filler and measured by ASTM D2240, with typical values from 25 Shore A to 50 Shore A. Tensile strength is tested to ISO 37:2017, and tear strength to DIN ISO 34-1. For a 30 Shore A coolant-seal compound, tensile strength is generally 6.0–8.0 MPa, elongation 350–550%, and tear strength 12–18 N/mm. A process conflict arises when RH-Vi1324 loading exceeds 15 phr in filled compounds: the extrudate swells and loses green strength before curing, requiring screw speed below 30 rpm on a 45 mm extruder. The terminal products are radiator seals, oven-door gaskets, and ignition cable jackets.

    When Hydrogen-Blow Foaming Shifts Density and Cell Structure in Silicone Sealing Profiles

    Silicone foam tapes and gaskets are produced with RH-Vi1324 as the vinyl-terminated fluid in an addition-cure, hydrogen-blown system. The formulation combines 100 parts vinyl silicone oil, 5–20 parts hydride-terminated or pendant-hydride polysiloxane, 0.5–2.0 parts distilled water or short-chain hydroxy silicone fluid, and a platinum catalyst at 10–20 ppm Pt. The onset of hydrogen evolution begins when the mixed compound reaches 40–60°C; simultaneous crosslinking and gas nucleation must be balanced to avoid coalescence. The material is dispensed into closed or open moulds and cured at 80–120°C for 10–30 min. Density is controlled from 0.25 g/cm³ to 0.60 g/cm³ by varying the hydride-to-hydroxyl ratio and the mixing vacuum level; density is measured by ASTM D792 or ISO 1183-1:2019. Cell structure is characterized by cross-section microscopy, and compression set is evaluated according to ISO 815-1:2020 after 50% compression at 100°C for 22 h. For flame-retardant sealing profiles, alumina trihydrate is added at 40–80 phr, but the formulation becomes shear-thinning and requires a rotor-stator mixer at 1,000–2,000 rpm before compounding. The foam meets UL 94 V-0 at 3 mm thickness when the alumina trihydrate loading is above 60 phr, although tensile strength drops below 0.8 MPa. The main process failure is cell collapse caused by adding water above 2.0 phr or by curing below 80°C, which leaves unreacted Si-H groups that continue to evolve hydrogen during storage. Terminal goods are cell-closed edge-seals for battery enclosures, HVAC gaskets, and railcar window profiles.

    RH-Vi1324 is used in compression moulded silicone keypad compounds where durometer, contact fatigue, and residual peroxide content are controlled simultaneously. The compound is mixed in a kneader at 30–40°C with 100 phr vinyl polymer, 25–40 phr fumed silica, 2–5 phr MQ resin, and a platinum cure package at 0.5–1.0 ppm Pt. The Si-H:Si-Vi molar ratio is held at 1.4:1 to 1.7:1; higher hydride levels produce compression set below 15% but reduce elongation below 250%. The compound is sheeted to 2–5 mm thickness and compression moulded at 150–170°C for 5–10 min under 8–12 MPa moulding pressure. Durometer is checked by ASTM D2240, with typical values between 30 Shore A and 60 Shore A. Tear strength is measured by DIN ISO 34-1, elongation by ISO 37:2017, and rebound resilience by ISO 4662:2017. Keypad buttons produced from the compound are subjected to 1,000,000 cycles of actuation at 25°C; the force-displacement curve retains 80% of initial peak force when the Si-H:Si-Vi ratio is above 1.4:1. A production bottleneck occurs with high-hardness formulations above 60 Shore A: filling the microcavities requires mould temperatures above 160°C and prolonged flow time, but the compound skin-cures on the heated tool after 60 s, causing knit lines. The terminal articles are membrane switches, calculator keypads, and industrial control-panel buttons.

    Compliance matrix applicable to cured RH-Vi1324 articles
    Standard or regulationTest method or clauseRelevant endpoint
    FDA 21 CFR 177.2600Rubber articles for repeated food contact; extraction in hexane and distilled waterExtractables, sensory transfer
    ISO 10993-5:2009Cytotoxicity evaluation for medical devicesCell viability, leachate toxicity
    USP Class VISystemic injection and implantation testsAcute systemic toxicity, irritation
    IEC 60243-1Electric strength of insulating materialsDielectric breakdown voltage
    RoHS Directive 2011/65/EURestriction of lead, mercury, cadmium, hexavalent chromium, PBB, PBDECd below 0.01 wt%, others below 0.1 wt%
    REACH Regulation (EC) No 1907/2006SVHC declaration, Article 33 communicationSubstance screening, safe use information
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    Certification & Compliance
    More Introduction

    Vinyl Terminated Silicone Oil RH-Vi1324 is a linear polydimethylsiloxane carrying terminal vinyldimethylsilyl groups, supplied as a clear, colorless viscous liquid. The terminal arrangement distinguishes it from polydimethylsiloxane fluids with pendant vinyl substitution or trimethylsilyl end-blocking, because platinum-catalyzed hydrosilylation with a poly(hydrogenmethyl)siloxane crosslinker consumes predominantly the two chain termini. This produces a more defined average molecular weight between crosslinks than a random pendant vinyl distribution at equivalent vinyl content. The structural control is relevant in addition-cure liquid silicone rubber, low-shrinkage encapsulation, and release coatings where predictable modulus, low outgassing, and reproducible cure are required.

    Chemical Identity and Terminal Vinyl Architecture

    The material is commonly described as a dimethylvinyl-terminated dimethylpolysiloxane and is assigned CAS 68083-19-2 in technical literature. RH-Vi1324 is a reactive intermediate rather than a finished silicone elastomer. Terminal vinyl concentration is determined by iodometric titration and reported in millimoles of vinyl per gram. The acceptance window for RH-Vi1324 is normally centered near 0.12–0.14 mmol/g, with kinematic viscosity controlled to 1,000–1,500 mm²/s at 25 °C using calibrated capillary viscometers per ISO 3219:2021 and ASTM D445. Volatile content after 3 h at 150 °C is specified below 1.0 % by mass when tested according to ISO 3251:2019. These parameters are not independent; broadening of the molecular weight distribution can lower viscosity without changing total vinyl content, which is why both viscosity and vinyl content are specified on the certificate of analysis.

    Typical acceptance parameters for RH-Vi1324
    ParameterTypical range or limitTest method
    Kinematic viscosity at 25 °C1,000–1,500 mm²/sISO 3219:2021, ASTM D445
    Vinyl content0.10–0.16 mmol/gIodometric titration, titrant standardized to GB/T 601
    Volatile content≤ 1.0 % by massISO 3251:2019
    Refractive index at 25 °C1.403–1.406ASTM D1218-21
    Density at 25 °C0.97–0.98 g/cm³ISO 2811-1:2020

    Actual lot-specific data on the certificate of analysis supersedes typical ranges; RH-Vi1324 is not a certified reference material. In production-scale planetary mixers of 200 L working capacity, the fluid is combined with hydrophobic fumed silica after surface treatment. A planetary blade operating at 20–25 °C and 30–60 rpm yields dispersion without exceeding 45 °C, above which platinum-catalyzed hydrosilylation can initiate prematurely if inhibitor concentration falls below 0.05 % of total formulation mass. Viscosity drift greater than ±5 % after 24 h under nitrogen blanketing typically indicates moisture ingress or incomplete sealing of the mixer shaft.

    Chain-End Vinyl Distribution Controls Network Crosslink Density

    Because the vinyl groups occupy only the terminal positions, the molar mass of the polymer directly sets the maximum mesh size of the cured network. The terminal vinyl concentration is therefore the controlling specification rather than viscosity alone. A viscosity shift of ±10 % without a proportional change in vinyl content may indicate a broadened molecular weight distribution, which alters the balance between elastic chain segments and dangling chain ends. In hydrosilylation, the stoichiometric ratio of Si-H to Si-Vi is commonly adjusted to 1.2:1 to 1.8:1. Ratios below 1.2:1 can leave unreacted vinyl groups and produce tacky surfaces, while ratios above 2.0:1 may generate hydrogen gas or increase post-cure stiffness through secondary hydrosilylation. For RH-Vi1324, terminal distribution reduces the probability of chain-looping defects associated with low-molecular-weight pendant-vinyl fluids, but the maximum crosslink density at full conversion is lower than that of a random copolymer with the same vinyl content per kilogram.

    Platinum-catalyzed hydrosilylation of terminal vinyl groups follows an exothermic addition mechanism. Non-isothermal differential scanning calorimetry at 10 K/min under nitrogen typically records an onset temperature between 60 °C and 80 °C for uninhibited formulations. Addition of 0.02–0.1 wt% 1-ethynyl-1-cyclohexanol shifts the onset above 90 °C and extends pot life. Isothermal rheometry at 120 °C commonly gives a t90 cure time of 2–5 min depending on platinum concentration, but this must be validated for each batch because platinum residues in shared production equipment can catalyze premature gelation. A t90 below 90 s at 100 °C is often an early indicator of catalyst cross-contamination rather than a batch variation in RH-Vi1324 itself.

    How Does RH-Vi1324 Compare with Hydroxy-Terminated and Pendant-Vinyl Silicone Oils?

    RH-Vi1324 does not undergo condensation cure with tetraethyl orthosilicate, and it does not release water or methanol during cure. Compared with trimethylsilyl-terminated dimethyl silicone oil, it is not sufficiently inert for use as a purely non-reactive lubricant because the chain ends are reactive in the presence of platinum or peroxide. Compared with multi-vinyl pendant fluids, the terminal product provides lower crosslink density at a given total vinyl content and is therefore selected for low-modulus, high-elongation addition-cure gels.

    Comparison of reactive silicone fluid classes
    Product classReactive group locationCure mechanismNetwork density at equal vinyl content
    Hydroxy-terminated PDMSTerminal silanolCondensation with alkoxysilanesModerate; moisture or alcohol byproducts
    Trimethylsilyl-terminated PDMSNon-reactive terminal trimethylsilylNoneNot applicable; diluent only
    Pendant vinyl PDMSRandom vinyl side groupsAddition cureHigher at equal vinyl content
    High-vinyl silicone oilTerminal and pendant vinylAddition cure or chain extensionVery high; brittleness risk if over-added
    RH-Vi1324Terminal vinyldimethylsilylAddition cureControlled mid-range density

    In low-modulus addition-cure gels, RH-Vi1324 is blended with a hydride-functional crosslinker and a platinum catalyst. Hardness after full cure is measured with a durometer in the Shore A or Shore 00 scale; final hardness is adjusted by varying the Si-H/Si-Vi ratio and the molecular weight of the crosslinker. For encapsulation, the fluid is mixed with phenyl silicone resins if refractive index above 1.50 is required, because the pure terminal vinyl PDMS fluid has a refractive index of 1.403–1.406. In flexible mold rubber, tear strength is determined by ISO 34-1:2022; terminal vinyl networks generally produce lower tear strength than random pendant vinyl networks at equal hardness because of the lower crosslink density.

    When Low Volatile Loss Becomes Critical in Confined-Cure Applications

    Applications requiring minimal volatile condensate under vacuum or in sealed optical assemblies impose limits on low-molecular-weight siloxane cyclics. RH-Vi1324 is controlled for volatile content by thin-film stripping or molecular distillation. The ISO 3251:2019 method measures non-volatile matter; however, electronic and aerospace applications may also require headspace gas chromatography or thermal desorption GC-MS to quantify D4, D5, and D6 cyclic siloxanes. A total cyclic siloxane concentration below 100 mg/kg is often required. Components fabricated from RH-Vi1324 may need post-cure at 200 °C for 4 h to reduce outgassing before testing according to ASTM E595, with total mass loss below 0.5 % and collected volatile condensable materials below 0.1 %. Published data for RH-Vi1324 under ASTM E595 in specific optical encapsulant geometries is limited; qualification must be performed on the final article rather than on the raw fluid alone.

    Mixing, Dispersion, and Deaeration Requirements in Production Equipment

    In a two-component addition-cure system, side A contains RH-Vi1324, a hydride-functional prepolymer, and an inhibitor; side B contains RH-Vi1324, platinum catalyst, and filler. The two components are mixed through a static mixer of 24 elements and injected at 20–40 °C. Because terminal vinyl fluids exhibit lower shear thinning than branched or heavily filled systems, pressure drop in the static mixer remains more stable. Filler loading above 20 wt% increases viscosity and can raise mix head temperature above 45 °C, shortening pot life. Deaeration at −0.095 MPa for 10 min in a sealed vessel is used before casting; incomplete deaeration produces air bubbles that act as stress concentrators in tensile specimens tested per ISO 37:2017. For high-speed injection molding of liquid silicone rubber, clamp force is maintained at 1,000–2,000 kN for multi-cavity tools, with short-shot compensation triggered by cavity pressure sensors calibrated to ISO 17025.

    In solvent-free release coating, RH-Vi1324 is blended with a hydride crosslinker and a platinum inhibitor/catalyst system at a coat weight of 0.6–1.2 g/m². Curing at 120–150 °C for 30–60 s produces a release layer. Release force against an acrylic adhesive is typically 3–10 cN/25 mm when measured by FINAT FTM 11; exact values depend on the Si-H/Si-Vi ratio, film thickness, and post-cure temperature. For release coating lines, viscosity drift above ±5 % can produce coating weight variation greater than ±0.1 g/m², which is detectable as uneven release performance.

    Avoiding Catalyst Poisoning and Premature Gelation in Multi-Purpose Plants

    RH-Vi1324 should be stored in sealed, nitrogen-blanketed containers at 5–30 °C. Ambient moisture does not hydrolyze the terminal vinyl group but can affect filled formulations. The product is exposed to the same catalyst poisoning risks as other addition-cure silicone fluids: organotin condensation catalysts, sulfur-containing release agents, and amine-functional silanes should be excluded from shared processing lines. Platinum loadings as low as 2 ppm in the final formulation can be deactivated by cross-contamination from a tin-catalyzed RTV line into an addition-cure metering pump. Cleaning solvent selection is limited to aliphatic hydrocarbons or volatile methyl siloxanes; ketones and alcohols may leave adsorbed films on wetted surfaces and are not always effective for removing platinum-poisoning residues. The raw fluid has not been registered for food-contact use under FDA 21 CFR or for implantable medical devices under ISO 10993; regulatory compliance must be verified for the formulated article. In high-humidity production environments above 60 % RH, fillers should be pre-dried at 120 °C for 2 h before compounding to prevent porosity caused by water interaction with the hydride-functional component.