Products

8-Methylisoquinoline

    • Product Name: 8-Methylisoquinoline
    • Alias: 8-Methyl-1-azanaphthalene
    • Einecs: 219-423-0
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    747807

    Name 8-Methylisoquinoline
    Cas Number 6318-41-6
    Molecular Formula C10H9N
    Molecular Weight 143.19 g/mol
    Appearance Light yellow to brown solid
    Boiling Point 273-275 °C
    Melting Point 39-41 °C
    Density 1.08 g/cm³
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Iupac Name 8-Methylisoquinoline
    Pubchem Cid 41973

    As an accredited 8-Methylisoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 8-Methylisoquinoline, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with product name, CAS, and hazard warnings.
    Shipping 8-Methylisoquinoline is shipped in tightly sealed containers to prevent leakage and contamination. It is typically packed following local and international hazardous material regulations. The chemical should be stored in a cool, well-ventilated area, away from sources of ignition, and handled by trained personnel wearing appropriate protective equipment. Transport under UN 2810 (toxic liquid, organic, n.o.s.) regulations may apply.
    Storage 8-Methylisoquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, sources of ignition, and incompatible substances such as oxidizers. It should be kept at room temperature and protected from moisture. Proper labeling and secure storage are essential to prevent accidental exposure or spillage. Store according to local regulations for hazardous chemicals.
    Application of 8-Methylisoquinoline

    Applications of 8-Methylisoquinoline in Industrial Manufacturing

    8-Methylisoquinoline is a key intermediate used by specialty chemical manufacturers and downstream formulators in several industrial applications, particularly across the pharmaceutical, agrochemical, pigment, and specialty materials sectors. Our production process ensures the supply of high-purity material, meeting stringent purity and quality benchmarks required for downstream synthesis and large-scale manufacturing operations.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical producers utilize 8-Methylisoquinoline as a building block in the synthesis of specific small-molecule APIs, including central nervous system drugs and anti-tubercular compounds. It reacts in step-growth synthesis, most frequently in the isoquinoline motif construction or further functionalization. Robust impurity control and traceability at this stage ensure batch conformity throughout the value chain.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF, Ph. Eur., JP monograph references (where applicable to downstream APIs)
    • 21 CFR Part 210/211 (US FDA cGMP requirements for drug substance manufacturing)
    • EU GMP Annex 8 (Sampling of Starting and Packaging Materials)

    Typical usage ratio

    • 0.2–1.5 molar equivalents as starting material in stepwise synthesis, depending on the specific pharmaceutical target and downstream functionalization requirements

    Downstream process integration

    • Initial condensation reaction or N-alkylation in multi-step organic synthesis, followed by purification and introduction into the API intermediate chain

    Final product types

    • Antitubercular APIs (e.g., ethambutol analogs)
    • CNS-active drug candidates with isoquinoline backbone
    • Alkaloid-derived APIs
    • Research-grade reference compounds

    2. Agrochemical Intermediate for Herbicide and Pesticide Synthesis

    Agrochemical formulators employ 8-Methylisoquinoline as a core nucleophile or condensation substrate for the preparation of advanced intermediates in the production of specific herbicides and fungicides. The compound offers favorable reactivity in constructing heterocyclic motifs and can serve as a direct precursor for several quinoline-type crop protection agents, with process safety controls essential to minimize residual content.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management Systems for chemical intermediates
    • REACH Regulation (EC) No 1907/2006—Chemical Substance Registration in the EU
    • OECD Guidelines for the Testing of Chemicals—Purity & impurity profiling for pesticides
    • FAO/WHO JMPR specification for pesticide intermediates

    Typical usage ratio

    • 0.3–2.0 molar equivalents depending on the target active compound's synthetic route; stoichiometry optimized for yield and minimization of by-products in large-scale batch or flow regimes

    Downstream process integration

    • Serves as a nucleophilic reactant during cyclization or condensation steps in heterocycle formation, generally introduced post-hydrolysis and preceding terminal function modification

    Final product types

    • Heterocyclic herbicide actives
    • Systemic fungicide intermediates
    • Anti-insect biocides containing methylisoquinoline rings
    • Custom agrochemical research standards

    3. Pigment and Dye Intermediate in Fine Chemical Manufacturing

    Producers of high-performance pigments and dyes incorporate 8-Methylisoquinoline during synthesis of specialized colorants, leveraging its aromatic reactivity for constructing chromophoric structures. This application requires rigid controls on residual metallic and organic impurities in compliance with international safety standards for colorant production. Incorporation stage and purity dictate color stability and intensity in downstream pigment systems for plastics and inks.

    Industry compliance standards

    • EN 71-3:2019 (Migration of certain elements in colorants for toys and coatings)
    • ISO 4618:2014 (Paints & varnishes—Terms and definitions for pigment intermediates)
    • REACH compliance for colorant substances, Annex XVII
    • ASTM D3723 (Organic pigments—Quality assurance for intermediates)

    Typical usage ratio

    • 0.1–0.4 equivalents as a precursor, varying with dyestuff or pigment complexity, especially where multistep condensation and ring modification are required

    Downstream process integration

    • Enters the dye or pigment molecule construction during ring functionalization, preceding final azo or anthraquinone group attachment or further alkylation

    Final product types

    • High-stability ink pigments for offset and digital printing
    • Organic dyes for synthetic fiber coloration
    • Colorant precursors for plastics and elastomers
    • Fluorescent pigment concentrates for industrial applications

    4. Building Block for Advanced Material Synthesis (Polymers & Specialty Resins)

    Producers of specialized polymers and advanced performance resins integrate 8-Methylisoquinoline as a monomeric or oligomeric synthesis intermediate, particularly for introducing nitrogen heterocycles that can enhance thermal resistance or specialty adhesion. Control over amine content and cationic impurities at this stage determines final polymer property reproducibility, with process integration driven by demand from electronics, aerospace, and surface coatings sectors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for specialty chemical intermediates
    • RoHS Directive 2011/65/EU—Restriction of Hazardous Substances relevance in electronics materials
    • UL 94 (Flammability testing for plastic materials)
    • ASTM D5630 (Residue on ignition standard test for polymer precursors)

    Typical usage ratio

    • 0.05–0.3 weight fraction as a co-monomer or intermediate segment, adjusted based on target chain length, resin matrix compatibility, and end-use thermal or chemical resistance parameters

    Downstream process integration

    • Introduced in oligomerization or pre-polymerization phase; can function as a backbone or pendant group for polyimides, specialty polyamides, or custom resin chemistries requiring aromatic heterocycles

    Final product types

    • Polyimides and high-temperature thermoplastics
    • Adhesive resins for electronics encapsulation
    • Coating resins with enhanced bond strength
    • Advanced composites for aerospace and performance materials

    Free Quote

    Competitive 8-Methylisoquinoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    8-Methylisoquinoline: A Closer Look from a Manufacturer’s Perspective

    Introduction to 8-Methylisoquinoline

    We’ve been running continuous synthesis and purification lines dedicated to isoquinoline derivatives for decades. Among these intermediates, 8-Methylisoquinoline stands out with a distinct set of practical benefits. Many customers approach us seeking quality building blocks for their research or ongoing chemical production. Our extensive experience with high-purity heterocyclic compounds guides us to refine batches of 8-Methylisoquinoline that meet rigorous standards without losing focus on real-world application needs.

    8-Methylisoquinoline—often written chemically as 8-methyl-1-azabenzene—features a methyl group in the meta position on the benzene ring fused to a nitrogen-containing heterocycle. This simple modification delivers a molecule prized in the discovery and manufacture of active pharmaceutical ingredients, agrochemicals, and specialty materials. It’s not just a niche curiosity; the compound fits neatly into the toolkit of medicinal and process chemists searching for selectivity and reactivity unavailable from unsubstituted isoquinolines.

    Manufacturing Experience: Quality in Every Batch

    The demand for methylated isoquinolines has not plateaued. Over the years, we noticed researchers depend on reliable supply and unambiguous chemical profiles, whether they’re developing new kinase inhibitors or exploring advanced electronic materials. The synthesis requires accuracy—chlorination, catalytic cyclization, or selective methylation only get you so far. Robust quality control is just as important. Every lot on our line passes through a battery of analytical checks: NMR, HPLC, mass spec, and Karl Fischer for moisture content.

    We do not outsource purification. Each finished batch of 8-Methylisoquinoline is purified on in-house columns, ensuring actual purity lands above 99%, with any traces of isomeric or starting material impurities falling well below the narrow thresholds needed by serious process chemists. Our team frequently consults with partners to troubleshoot downstream reactivity, since even minor contamination will influence sensitive transformations such as Pd-catalyzed couplings, N-oxidation, or Grignard reactions.

    Specifications Matter for Real-World Applications

    8-Methylisoquinoline exits our facility colorless or straw yellow, in solid or occasionally crystalline form, with true melting points and clean chromatographic signatures to match. Each customer batch includes a certificate of analysis, summarizing the observed GC, NMR, and residual water. Minimum order sizes begin at tens of grams, scaling up to multi-kilogram quantities as required. Specific lots ship in inert packaging, and we track all containers against batch records for traceability and regulatory reporting.

    What consistently comes up during technical discussions is the practical value of robust chemical performance. Users might aim to run oxidations, halogenations, or Suzuki couplings that rely on reproducible starting material. Instead of chasing after generalized purity claims, our technical staff digs deeper. Poor solubility or extraneous peaks in the NMR quickly translate to lost time in lab or on the production line. Every gram matters when you’re working with narrow windows for yield and time.

    Core Differences: 8-Methylisoquinoline vs. Standard Isoquinolines

    Chemists often ask where the performance of 8-Methylisoquinoline splits from basic isoquinoline. Real differences shine through both in the bench reaction flask and analytical data. Adding a methyl group at the 8-position subtly tunes reactivity: electron distribution shifts, bond-dissociation energies change, and aromatic ring activation responds to different reagents. You’ll see this when others try to run regioselective halogenations or metal-catalyzed functionalizations—what works for simple isoquinoline doesn’t always translate.

    Pharmaceutical researchers leverage this behavioral shift to design molecules with better target selectivity or metabolic profiles. Many medicinal chemistry programs lean on 8-Methylisoquinoline as a scaffold because the methyl substituent can block unwanted oxidative metabolism or steer the direction of downstream modifications. The result is a starting material tailored not only for tractability in scaled reactions, but also for unique biological results.

    On the process side, the boiling point, reactivity in transition metal catalysis, and crystallization properties respond to methyl substitution. We document subtle but important shifts in solubility (both in polar and non-polar solvents), refining downstream isolation steps for customers. Someone scaling up for bulk production will see lower byproduct formation in processes susceptible to aromatic oxidation, meaning less waste and easier purification overall.

    Real-World Usage and Industry Feedback

    Users from multinationals to startups report feedback from their process development groups. Some buyers require just small lots for assay development, but most transfer our material to pilot or GMP lines. Our product supports projects from drug lead optimization through to kilo-lot production, handling stringent ICH Q7 and FDA expectations on documentation and materials management.

    In the world of materials chemistry—OLEDs, specialty ligands, or custom polymers—isoquinoline analogs such as this one allow for direct insertion of unique properties. Polymers and advanced coatings sometimes require an extra degree of hydrophobicity or electronic tuning not possible through core isoquinoline. The methyl group creates that necessary distinction. Often, new patents cross our desks detailing electronic property enhancements, all owing to a subtle switch at the 8-position.

    One research partner, looking at novel agrochemical actives, highlighted reduced toxicity and improved in vivo stability simply by moving from non-methylated to 8-methyl analogs. Others pursuing CNS candidates commented on improved blood-brain barrier penetration, again owing to the methyl group. We don’t just deliver a shipment; our technical team follows up to see which synthetic routes prove most efficient and whether alternate purification steps become necessary.

    Supporting Claims with Proven Data and Practice

    We aren’t just guessing. Dozens of customer projects now rely on 8-Methylisoquinoline’s behavior in functionalization reactions—hydroxylation, cross-coupling, nitration, and beyond. Literature references show that the methyl substituent changes yields and selectivity for core chemical reactions. In Suzuki-Miyaura reactions, for example, the 8-methyl analog often displays higher selectivity and easier work-up, credited to the electronic effects from methylation. In N-oxidation reactions, conversion rates shift and produce cleaner byproducts. Analytical reports from our customers repeatedly show higher chemical yields, cleaner signals on HPLC, and more stable performance during scale-up.

    Our hands-on data lines up with these published findings. One process route, switching only the isoquinoline for our methylated grade, raised the isolated yield by 15% and cut side-product formation almost in half. Such shifts matter when producing dozens of kilograms in a commercial batch, trimming both time and raw material costs. Alleviating bottlenecks in isolation also means reduced operator risk. Staff spend less time handling multiple chromatography runs or refining crystal forms.

    Addressing Industry Challenges: Reliability, Purity, Safety

    Running a chemical plant means facing everything from regulatory audits to daily batch-to-batch consistency. We invest in closely linked production and quality assurance teams, using proprietary methods that keep impurities and byproducts far below published pharmacopeia and industrial standards. Our stability testing spans months, confirming the methyl group stays intact with no evidence of N-oxide or dimer buildup, even after extended storage and repeated opening of containers. Consistent heating, cooling, and handling protocols cut down on batch variation—a factor that can derail even advanced process experiments.

    No batch leaves the site until safety and data sheets match internal and global Compliance requirements. All relevant hazard labels and UN shipping documentation ship with orders. Sometimes we go further—sealing drums under nitrogen, applying tamper-proof tapes, or running supplementary GC–MS analyses if a customer's method picks up trace unidentified peaks.

    Customers sometimes discuss issues with specifications on materials from brokers or lab chemical houses—variation in purity, unexpected reactivity, or shipping delays. Direct production eliminates most of these headaches. Orders never spend time in third-party warehouses, ingredients never linger unmonitored, and support comes from the chemists actually responsible for manufacturing.

    Environmental and Regulatory Aspects

    Modern chemical manufacturing gets scrutinized for both process safety and environmental impact. Any methylated aromatic, including 8-Methylisoquinoline, needs responsible sourcing and controlled emissions. Our facility deploys closed-loop solvent recovery on all major steps, with real-time VOC monitoring in production zones. Waste streams get pre-treated to break down aromatic traces before off-site handling.

    As regulatory agencies raise expectations, we document not just finished-product quality, but also every critical process control. Chain of custody stays locked down from raw material intake through lot release. We support major international compliance systems—REACH, TSCA, NMPA, and GHS—ensuring customers can import, handle, and use our material anywhere without late-stage surprises. Dedicated regulatory staff adapt documentation packs as new global requirements or customer audits arise. Risk-based assessments—worst-case exposure, occupational safeguards, and transportation classification—continually evolve in response to changing law and technical understanding.

    Continuous Improvement Based on Customer Collaboration

    Staying in front of the field means listening to chemists putting 8-Methylisoquinoline to work in tough settings—multistep process syntheses, medicinal chemistry programs, or scale-up projects for next-generation materials. Our staff meet routinely with R&D groups running into bottlenecks, providing extra characterization or alternate downstream purification protocols. On request, we generate additional COAs customized for in-house method validation.

    We’ve worked through NMR fingerprinting variations with partners who experienced new impurities after modifying work-up routines. Lead process engineers often approach us for alternate packaging—sometimes powder, sometimes more granular, to fit specialty reactors. Others call for extra desiccant structures to maximize long-term storage stability in high-humidity settings. We don’t treat feedback as a box to check; our technical account managers push real updates down to operators and QA, baking lessons learned into every following batch.

    A case in point: one bulk customer flagged an off-odor concern during warehouse storage, which we traced back to a minor, thermally-induced side reaction. We overhauled our shipping schedule to keep exposure times low, upgraded interior coatings on our large drums, and started post-shipment stability testing to close the gap. The outcome: improved shelf-life, verified by both customer and internal stability trackers.

    Supporting R&D and Custom Projects

    Not all uses for 8-Methylisoquinoline fit standardized catalog needs. Med chem and materials teams regularly seek derivatives—brominated, hydroxylated, functionalized—often too specialized for distribution by trading houses. Our flexible production lines allow quick conversion to custom analogs, preserving the same analytical rigor applied to standard runs. Because our chemists also manage process development, scale up for custom projects rarely hits a wall due to unfamiliar reaction routes or solvent incompatibility.

    Supporting early innovation means moving quickly. Researchers regularly need fast access to high-purity intermediates without the time lag involved in tech transfer. We turn around custom modifications—fluoro-, cyano-, or alkyl substitutions—starting from our 8-Methylisoquinoline core, delivering full analytical packages up to kilo scale. Our ongoing practice involves not only listening to proposed modifications but stress testing feasibility in-house, feeding back timelines and realistic risk points to project leads.

    Learning from Industry Trends and Academic Developments

    Keeping close contact with both applied R&D customers and academic groups reveals shifting trends in methylated isoquinoline applications. Published studies identify new targets in kinase inhibition, fluorescent probe scaffolds, or as anchors in C–H activation methodologies. We note an uptick in patent filings covering next-wave CNS and oncology drugs centered on methyl-substituted isoquinolines, underlining the expanding value of this relatively humble intermediate.

    Trade journals and preprints indicate increasing efforts to expand green chemistry for aromatic nitration and functionalization—less corrosive reagents, lower energy, reduced hazardous byproducts. In response, our process team continues to invest in greener reagents and higher solvent recovery rates, pushing beyond statutory minimums on energy use and waste minimization. This approach draws direct feedback from customer audits and environmental scorecarding, informing future expansions or upgrades.

    Supporting Innovation Through Supply Chain Resilience

    The events of the last several years—supply chain interruptions, raw material shortages, logistical bottlenecks—demonstrate how easily delays cascade through research and manufacturing. We learned to anticipate and build inventory buffers for key starting materials, including aromatic bases and specialty reagents, ensuring production lines do not stall during market upswings or global disruptions.

    Rather than relying on outside distributors for logistics, we coordinate directly with hazmat-certified carriers, reducing breakage and safeguarding product integrity in transit. Each load moves under our documented protocols, with temperature and humidity tracking tags attached for critical shipments. This degree of supply chain oversight shapes how our customers plan procurement, supporting long-term R&D programs where continuity matters more than one-off pricing.

    Advice for Selecting a Supplier—Direct from the Source

    Many buyers scrutinize only price per gram or kilo when weighing suppliers for methylated heterocycles. From a practical perspective, feedback from manufacturing partners points to three priorities before cost: batch reproducibility, clear analytical traceability, and immediate technical support in case of downstream process surprises. One-off purchases from traders often fit catalogue price lists, but real-world process managers choose suppliers who will walk the last mile—trouble-shooting synthetic issues, offering smarter packaging, tweaking analytical reports on request.

    Direct manufacturing expertise matters. If you encounter unexpected spots in the TLC or off-target peaks on HPLC after switching to a new source, tracking the problem to its roots becomes quicker with a team that handled both development and full-scale runs. This upstream-downstream communication forms the backbone of our repeat business: chemists prefer suppliers who can answer “how was this made?” and “what was the worst impurity detected?” with the same level of detail an internal colleague would provide.

    Conclusion: Partnering for Results

    Chemical manufacturing revolves around more than just synthetic prowess. Our role producing 8-Methylisoquinoline links us directly to researchers and process teams driving efforts in pharmaceuticals, materials science, and advanced chemistry. We bring decades of bench and production experience to each batch, ensuring specifications align with practical needs, compliance matches global expectations, and that every gram supports breakthrough research and commercial success.

    The details of manufacturing, packaging, and support shape results—yield, purity, safety, innovation. Whether you’re scaling a new pathway, testing a suite of analogs, or needing fast-turnaround kilos with complete documentation, the value comes from deep experience married to rigorous technical management. By building every lot of 8-Methylisoquinoline with end-use requirements in mind, we support not only our clients’ present needs but set a foundation for ongoing discovery and application in the most demanding chemical environments.

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