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2,4-Diphenyl-4-Methyl-1-Pentene

    • Product Name 2,4-Diphenyl-4-Methyl-1-Pentene
    • Alias 4-Methyl-2,4-diphenyl-1-pentene
    • Einecs 242-318-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    603543

    Chemical Name 2,4-Diphenyl-4-Methyl-1-Pentene
    Molecular Formula C18H20
    Molecular Weight 236.35 g/mol
    Cas Number 19848-00-7
    Appearance Colorless to pale yellow oily liquid
    Boiling Point Unknown (predicted >280°C)
    Melting Point Unknown
    Density Approx. 0.97 g/cm³
    Refractive Index Approx. 1.570 (predicted)
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically ≥98% (as sold commercially)
    Flash Point Predicted >110°C
    Structure Type Alkene with diphenyl and methyl substituents
    Smiles CC(C)(C=CC1=CC=CC=C1)C2=CC=CC=C2
    Inchikey VYJFMLSHXVNNCP-UHFFFAOYSA-N

    As an accredited 2,4-Diphenyl-4-Methyl-1-Pentene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, with airtight screw cap, labeled with chemical name, CAS number, hazard pictograms, and handling instructions.
    Shipping 2,4-Diphenyl-4-Methyl-1-Pentene is shipped in tightly sealed containers, protected from light and moisture, and typically packaged in glass or compatible plastic bottles. The shipment adheres to standard chemical handling regulations, including labeling and documentation. Ensure ventilation during transport and avoid temperature extremes. Not classified as a hazardous material for routine shipping.
    Storage 2,4-Diphenyl-4-Methyl-1-Pentene should be stored in a tightly sealed container, away from light and moisture, at room temperature or below. Keep in a cool, dry, and well-ventilated area, separated from incompatible substances such as strong oxidizers. Ensure the storage area is equipped for flammable materials and clearly labeled. Use proper personal protective equipment when handling.
    Application of 2,4-Diphenyl-4-Methyl-1-Pentene

    Applications of 2,4-Diphenyl-4-Methyl-1-Pentene in Industrial Manufacturing

    2,4-Diphenyl-4-Methyl-1-Pentene is a specialty intermediate primarily leveraged in advanced polymer modification, high-performance resin production, and pharmaceutical synthesis. As a manufacturer, we support downstream partners in leveraging the molecular design benefits across sectors that require fine control over product architecture, purity, and end-use performance. The following application segments outline well-established industrial scenarios, highlighting real formulation practices, compliance expectations, and integration points readable to technical, R&D, and procurement professionals.

    1. High-Performance Polyolefin Production

    Major polyolefin producers utilize this molecule to tailor-make specialty olefin copolymers for demanding mechanical and optical applications. The compound acts as a structure-directing comonomer that yields enhanced melt strength and tailored crystallinity when incorporated into advanced polyethylene and polypropylene grades via solution or slurry polymerization. Adjustments of the dosage level depend on the target product's clarity, flexibility, or impact resistance, especially for automotive and electrical markets. Strict control over raw material quality and homogeneity influences the performance and safety of downstream resins.

    Industry compliance standards

    • ISO 17855 (Polyolefin plastics – Definition and characterization)
    • ASTM D3350 (Standard classification for polyethylene plastic)
    • REACH Annex XVII (restrictions on certain hazardous chemical content)
    • UL 94 (Flammability of Plastics Materials for Parts in Devices and Appliances)

    Typical usage ratio

    • 0.1–2.5 wt% based on total monomer; adjusted upward for higher comonomer content or unique resin flexibility properties required in final grades

    Downstream process integration

    • Direct addition to bulk or solution-phase polymerization reactors as a co-monomer during main chain growth; precise metering ensures batch consistency and target molecular weight distribution

    Final product types

    • High-impact polypropylene compounds for automotive interiors
    • Clarity-modified polyethylene sheets and films for optical packaging
    • Engineering resin blends for home appliance housings

    2. Reactive Intermediate for Pharmaceutical Synthesis

    Process chemists in fine chemical manufacturing employ this compound as a key alkylating agent and side-chain precursor during the construction of complex molecular frameworks in active pharmaceutical ingredient (API) synthesis. Its phenylated structure provides favorable reactivity in constructing sterically demanding intermediates essential to small-molecule drugs. Process engineers tightly control addition conditions to avoid by-product formation, and documentation of traceability aligns with pharmaceutical GMP requirements.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia monographs (where applicable for relevant APIs)
    • USP 1078 (Good Manufacturing Practices for Bulk Pharmaceutical Excipients)
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 1–10 mol% relative to core substrate in multistep synthesis; exact loadings determined by route design, desired yield, and impurity profile limits

    Downstream process integration

    • Batch or semi-continuous addition in key C–C or C–N bond-forming steps, often as one of the first building blocks or as a terminal side-chain modifier during late-stage functionalization

    Final product types

    • Advanced intermediates for antihypertensive pharmaceutical actives
    • Chiral drug precursors with substituted phenyl groups
    • APIs and registered starting materials for oncology and CNS agents

    3. Specialty Resin Additive in LED Encapsulation Materials

    Engineering teams in optoelectronic resin formulation adopt this compound as a chain-modifying additive in encapsulant matrices used in LED devices. The high refractive index and excellent UV stability granted by its aromatic structure enable downstream substrate manufacturers to fine-tune light transmittance and component lifespan. Material addition and curing stages are closely monitored to prevent dispersion or phase separation that could adversely affect device quality.

    Industry compliance standards

    • IEC 60851-5 (Winding wires – Test methods for encapsulating resins)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances in electrical and electronic equipment)
    • JEDEC JESD22 (Reliability test methods for semiconductor devices)
    • ISO 14644 (Cleanrooms and associated controlled environments, relevant for electronic resin production)

    Typical usage ratio

    • 0.5–2.0 phr (parts per hundred resin); optimized for refractive index targets, heat resistance requirements, or device clarity according to end-use specification

    Downstream process integration

    • Dispersion into silicone or epoxy base during premixing prior to degassing and casting; controlled photoinitiator addition or thermal cure for completion of encapsulation

    Final product types

    • Epoxy or silicone encapsulant resins for LED chip packaging
    • High-index potting compounds for COB (chip-on-board) LED modules
    • Light-transmitting adhesives for backlighting and sensor assemblies

    4. Modifier in Advanced Photoinitiator Synthesis

    Producers of photoinitiators and UV-curable oligomers for digital printing and electronics industries incorporate this pentene derivative as a functional group donor or as a blocking group precursor in UV-reactive molecule synthesis. Its hydrocarbon skeleton introduces steric and photophysical stability, supporting improved shelf-life and performance under extended UV exposure in final polymers, coatings, and inks. Qualified facilities maintain trace control with continuous batch sampling throughout reaction scale-up.

    Industry compliance standards

    • ISO 27668-2 (Ink for UV-curable printing systems)
    • EN 71-3 (Safety of toys – migration of certain elements, relevant for toy coatings)
    • GHS Classification and Labeling for chemical safety communication
    • SGS Testing Requirements for photoinitiator content in coated consumer goods

    Typical usage ratio

    • 0.5–5.0 mol% in synthesizing photoinitiator molecules; formula optimization depends on desired reactivity, photobleaching stability, and compatibility with target resin systems

    Downstream process integration

    • Introduced as a functionalizing or capping agent during intermediate formation, prior to final purification and microfiltration of photoinitiator batches

    Final product types

    • UV-curable photoinitiator systems for industrial inks and varnishes
    • Specialized coatings for circuit board protection
    • Photocurable adhesives and 3D printing resin formulations

    5. Specialty Organic Synthesis Building Block for Liquid Crystal Compounds

    Manufacturers in the liquid crystal materials industry employ this raw material as a substituent for side-chain engineering in advanced mesogenic compound development. The product’s phenyl-rich structure supports molecular alignment and phase behavior, serving as a backbone modifier within custom liquid crystalline mixtures. Typical use cases aim to increase anisotropy, enhance alignment in electric fields, or tune birefringence for high-definition, bistable, or flexible display devices.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for specialty chemicals)
    • RoHS 2011/65/EU (for electronic display material restrictions)
    • REACH Registration (for high-purity custom organics)
    • IEC 61747 (LCD device safety and quality standards)

    Typical usage ratio

    • 0.3–1.2 wt% as a functional additive, ratio is fine-tuned through mixture screening for targeted optical and electro-optical characteristics in the final nematic or smectic blend

    Downstream process integration

    • Included during co-condensation or acylation stages of mesogen synthesis, followed by distillation and blending with other core and terminal group compounds

    Final product types

    • Bistable and high-contrast nematic liquid crystal mixtures for display panels
    • Specialty phase liquid crystals for optical communication modulators
    • Wearable device and foldable screen LC blends
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