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6-Methoxyisoquinoline

    • Product Name 6-Methoxyisoquinoline
    • Alias 6-Methoxy-1-azanaphthalene
    • Einecs 214-048-4
    • 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

    640437

    Iupac Name 6-Methoxyisoquinoline
    Molecular Formula C10H9NO
    Molecular Weight 159.19 g/mol
    Cas Number 607-26-9
    Appearance Off-white to pale yellow solid
    Melting Point 62-65°C
    Boiling Point 306°C
    Density 1.18 g/cm³
    Solubility In Water Slightly soluble
    Smiles COC1=CC2=C(C=C1)C=CN=C2
    Inchi InChI=1S/C10H9NO/c1-12-9-3-2-7-4-5-11-6-8(7)10(9)1
    Pubchem Id 12143
    Refractive Index 1.633

    As an accredited 6-Methoxyisoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 6-Methoxyisoquinoline, labeled with product name, CAS number, lot number, and safety warnings.
    Shipping 6-Methoxyisoquinoline is shipped in tightly sealed, chemical-resistant containers, clearly labeled according to regulatory requirements. The package is cushioned to prevent breakage and complies with international transport guidelines. Shipping is conducted via certified carriers, ensuring the compound remains stable and protected from moisture, heat, and light during transit.
    Storage 6-Methoxyisoquinoline should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Properly label the container and ensure it is kept in accordance with standard laboratory chemical storage practices.
    Application of 6-Methoxyisoquinoline

    Applications of 6-Methoxyisoquinoline in Industrial Manufacturing

    6-Methoxyisoquinoline serves as a valuable intermediate for multiple advanced manufacturing sectors. As a direct producer, we supply this raw material to established downstream industries with proven demand, focusing on its authentic applications across specialized production routes. Below, we present the main industrial use cases, outlining specific regulatory adherence, formulation roles, production integration, and real end products.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    The pharmaceutical industry incorporates 6-Methoxyisoquinoline in the synthesis pathway of certain antihypertensive drug actives, leveraging its aromatic scaffold for controlled transformations under cGMP guidelines. Formulation chemists introduce the compound during early-stage multi-step synthesis as a building block, resulting in targeted molecular architectures. The preparation process involves protection, methylation, and coupling stages, critical to the purity profile and regulatory compliance of the final API batches.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211: cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) monograph requirements
    • EDQM and USP compendial references as applicable for synthetic intermediates

    Typical usage ratio

    • Used between 0.15 and 0.35 molar equivalents relative to core API synthesis (ratio adjusted based on batch size and process efficiency goals)

    Downstream process integration

    • Introduced during ring construction or methoxy group introduction in the initial synthetic stage, followed by sequential functionalization and purification operations within the API manufacturing route

    Final product types

    • Bulk antihypertensive active pharmaceutical ingredients (e.g., derivatives used for calcium channel blockers, depending on the synthesis pathway)
    • Pharmaceutical intermediates for regulated market supply

    2. Synthesis of Isoquinoline-Based Agrochemical Actives

    Producers in the agrochemical sector rely on 6-Methoxyisoquinoline as a heterocyclic core for downstream transformation into selective herbicidal and plant growth regulatory actives. Process chemists utilize the compound under ISO 9001 management, incorporating it via catalytic alkylation and oxidative coupling reactions tailored to patented invention disclosures. Finished actives must meet stringent environmental and residue standards before market launch.

    Industry compliance standards

    • REACH Regulation (EC No 1907/2006) for chemical substance registration
    • ISO 9001:2015 Quality Management System for Agricultural Chemical Production
    • OECD Guidelines for Testing of Chemicals – Agrochemical registration studies
    • FAO/WHO Codex Alimentarius pesticide residue limits for active ingredients

    Typical usage ratio

    • 0.5%–2.0% by weight relative to total agrochemical active synthesis batch, with adaptation based on the target heterocycle substitution pattern

    Downstream process integration

    • Reactant charged at the initial condensation or cyclization stage in the multi-step synthesis of the isoquinoline-based agrochemical, followed by product isolation and purification

    Final product types

    • Technical grade herbicide actives
    • Functional intermediates for plant growth regulators
    • Registered crop protection raw actives for formulation lines

    3. Building Block for Organic Electronic Materials

    Manufacturers of high-performance organic semiconductors utilize 6-Methoxyisoquinoline in the construction of molecular structures engineered for specific optoelectronic properties. Facilities following JEITA and RoHS protocols employ this raw material within Suzuki-Miyaura cross-coupling stages to achieve fully conjugated frameworks, which contribute to functional polymer and small-molecule design for light-emitting diode, photovoltaic, and photodetector applications. Purity and trace impurity controls remain critical for device-grade yields.

    Industry compliance standards

    • JEITA ET-7304: Guidelines for Organic Materials in Electronics
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001: Environmental Management for Electronic Components
    • IEC 62474: Material Declaration for Products of and for the Electrotechnical Industry

    Typical usage ratio

    • 1.0–6.0 mol% in precursor preparation for polymer backbones or monomer coupling, precise proportion defined by targeted energy gap and processing protocol

    Downstream process integration

    • Charged into catalyst-assisted cross-coupling reactors for synthesis of π-extended core units, followed by downstream polymerization or oligomer isolation for application in electronic device fabrication

    Final product types

    • Organic light-emitting diode (OLED) materials
    • Organic photovoltaic active layers
    • Photodetector and optoelectronic thin films

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    The specialty colorant sector processes 6-Methoxyisoquinoline as a precursor for the production of high-performance dyes and pigments, attributing its nitrogen-heterocycle structure to desirable chromophore features. Industrial formulators dose the compound during targeted condensation or azo coupling reactions, typically aligning with textile, plastics, and specialty ink segment requirements. Batch-to-batch color consistency and compliance with toxicological limits are strictly monitored throughout these operations.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • EN 71-3 (Toy Safety Directive) for migration of certain elements in pigments
    • China GB 9685 additive provision lists for food contact materials, where applicable
    • ISO 9001:2015 Quality Systems in Fine Chemicals

    Typical usage ratio

    • Addition at 0.8–3.0% by weight of total synthesis mixture, rate varies with chromophore target and batch yield performance

    Downstream process integration

    • Introduced as the key aromatic source for ring-closure or direct azo-coupling stage in the organic dye production process; subsequent filtration and drying yield concentrated pigment dispersions

    Final product types

    • Textile and synthetic fiber dyes
    • High-fastness pigments for specialty inks
    • Plastic colorants with regulated migration profiles
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