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4-Bromoisoquinoline

    • Product Name 4-Bromoisoquinoline
    • Alias 4-Bromoisoquinolin
    • Einecs 205-989-5
    • 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
    VTB
    Specifications

    HS Code

    458089

    Product Name 4-Bromoisoquinoline
    Cas Number 16198-50-0
    Molecular Formula C9H6BrN
    Molecular Weight 208.06
    Appearance Off-white to light yellow solid
    Melting Point 48-52°C
    Boiling Point 310°C
    Density 1.54 g/cm³
    Purity Typically ≥98%
    Smiles Brc1ccc2nccc2c1
    Inchi InChI=1S/C9H6BrN/c10-8-3-1-2-7-6-11-5-4-9(7)8/h1-6H
    Solubility Slightly soluble in organic solvents
    Storage Temperature Store at room temperature, in a dry place
    Synonyms 4-Bromoisoquinoline; Isoquinoline, 4-bromo-

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

    Packing & Storage
    Packing The 4-Bromoisoquinoline is supplied in a 25g amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Shipping 4-Bromoisoquinoline is shipped in secure, sealed containers compliant with hazardous material regulations. Packaging ensures protection from moisture, light, and damage during transit. Shipments are labeled according to international chemical safety standards and accompanied by a safety data sheet. Delivery is handled by certified carriers specializing in chemical transport.
    Storage 4-Bromoisoquinoline should be stored in a tightly sealed container in a cool, dry, and well-ventilated place. Protect it from light, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature and clearly label the container. Ensure chemical storage areas are secure, and only trained personnel handle the substance following appropriate safety protocols.
    Application of 4-Bromoisoquinoline

    Applications of 4-Bromoisoquinoline in Industrial Manufacturing

    4-Bromoisoquinoline serves as a crucial advanced intermediate across several high-value synthetic pathways within the chemical industry. As a manufacturer with established production capabilities, we enable downstream partners to integrate this compound in demanding workflows, ensuring compliance, precision in formulation, and consistent quality in large-scale operations.

    1. Pharmaceutical API and Intermediate Synthesis

    Innovative pharmaceutical producers employ this material within multi-step syntheses for active pharmaceutical ingredients, particularly in heterocyclic frameworks for oncology and CNS indications. Its value resides in the bromine functionality, which facilitates regioselective coupling and functionalization steps performed under pharmaceutical GMP guidelines, accelerating the synthesis of complex isoquinoline-based drug candidates and registered actives.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopeia and US Pharmacopeia (as applicable for final API)
    • FDA 21 CFR Part 211 (where integrated into API stages in regulated markets)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Reactant molarities generally range from 0.1 to 0.5 mol per mol target API, adjusted based on the synthetic route's step count, scale, and target yield optimization.

    Downstream process integration

    • This compound enters medicinal chemistry and scale-up batches at early to mid-stage coupling and cyclization reactions, then is removed or transformed before isolation of the final API or advanced intermediate.

    Final product types

    • Anticancer active pharmaceutical ingredients (e.g., kinase inhibitors)
    • Complex CNS drug candidates containing isoquinoline motifs
    • Clinical trial material for small molecule therapies

    2. Agrochemical Active Ingredient Building Block

    Leading agrochemical manufacturers rely on this isoquinoline derivative as a halogenated scaffold for the modular synthesis of herbicide and insecticide actives. The brominated structure is suited for further functionalization via palladium-catalyzed cross-coupling processes, supporting the assembly of highly selective bioactive molecules under regulated production standards specific to crop protection chemistry.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Manufacture of Pesticides
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 (European market)
    • Relevant national chemical registration and environmental safety laws

    Typical usage ratio

    • Intermediate dosage typically 0.2–0.6 eq per final agrochemical active, with adaptation to the target molecule's synthetic core and functional group load.

    Downstream process integration

    • Initial entry occurs as a bromo building block for Suzuki or Buchwald–Hartwig couplings, with subsequent derivatization and purification before formulation into technical concentrates or final crop protection agents.

    Final product types

    • Selective herbicide active ingredients
    • Isoquinoline-derived insecticide actives
    • Seed protection chemistry intermediates

    3. OLED and Organic Electronics Materials Synthesis

    Producers of advanced organic electronic components incorporate this raw material for constructing highly conjugated isoquinoline derivatives, serving as precursors for blue and green emitters in OLED manufacturing. The precise configuration and electron-withdrawing bromine moiety allow for controlled cross-coupling assembly, contributing to high-purity and consistent batch quality essential in optoelectronic device production. Processing requirements align with stringent electronics-grade guidelines for purity and trace contaminants.

    Industry compliance standards

    • IEC 61249-2-21 halogen-free standards for base materials (for finished device compliance)
    • SEMATECH purity standards for organic electronic chemicals
    • ISO 9001:2015 and QC protocols for optoelectronic raw materials
    • RoHS Directive 2011/65/EU (where finished devices are exported)

    Typical usage ratio

    • Loadings generally 5–20% by weight in cross-coupling reaction mixtures, calculated based on target emitter yield and device layer deposition requirements.

    Downstream process integration

    • Material enters at the small molecule synthesis stage, typically handled via Buchwald–Hartwig or Suzuki–Miyaura coupling, followed by high-vacuum purification and crystalline isolation for subsequent thin-film deposition workflows.

    Final product types

    • Small-molecule organic emitters for OLEDs
    • Precursors for charge transport materials
    • Isoquinoline-functionalized intermediates for organic semiconductors

    4. Specialty Dye and Pigment Intermediate Production

    The fine chemical sector integrates this intermediate in manufacturing specialty dyes and pigments, especially those requiring high chroma and light fastness for high-performance plastics, fibers, or inkjet inks. The brominated nucleus enables unique color properties after subsequent substitution reactions. Industrial producers follow niche application standards, particularly in terms of migration, toxicity, and batch-to-batch reproducibility for sensitive consumer or industrial markets.

    Industry compliance standards

    • Oeko-Tex Standard 100 Annex 4 (where used in textile dye chain)
    • EN 71-3 (for pigments used in children’s products and toys)
    • ISO 787 and ISO 18314 for pigment testing and specification
    • REACH compliance for European market

    Typical usage ratio

    • Net consumption typically falls within 0.05–0.2 eq relative to colorant output, dependent on color depth requirements and secondary modification stages.

    Downstream process integration

    • The compound is utilized as an initial halogenated building block in nucleophilic aromatic substitution or as a coupling partner for expanding the aromatic system. Steps follow with pigment precipitation, filtration, and final formulation for end-use compatibility.

    Final product types

    • High-purity specialty dyes for plastics and synthetic fibers
    • Colorants for industrial inkjet formulations
    • Light-fast pigments for specialty coatings
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