Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

7-Methylisoquinoline

    • Product Name 7-Methylisoquinoline
    • Alias 7-Methyl-1-azanaphthalene
    • Einecs 206-660-0
    • 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

    292406

    chemical_name 7-Methylisoquinoline
    molecular_formula C10H9N
    molecular_weight 143.19 g/mol
    CAS_number 1837-58-7
    appearance Pale yellow to yellow solid
    boiling_point 272-274 °C
    melting_point 39-42 °C
    density 1.09 g/cm³
    purity ≥98%
    SMILES Cc1cccc2ncccc12
    InChI InChI=1S/C10H9N/c1-8-3-2-4-9-5-6-11-7-10(8)9
    solubility Slightly soluble in water, soluble in organic solvents

    As an accredited 7-Methylisoquinoline 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 7-Methylisoquinoline, securely sealed, labeled with hazard symbols, chemical name, and supplier details.
    Shipping 7-Methylisoquinoline is shipped in sealed, chemical-resistant containers to prevent contamination and degradation. It should be transported under cool, dry conditions, away from heat sources and incompatible materials. All shipments comply with relevant hazardous material regulations, including proper labeling and documentation for safe handling and regulatory compliance during transit.
    Storage 7-Methylisoquinoline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Ensure proper labeling and secure storage to prevent leaks or spills. Store at room temperature and follow all relevant safety, handling, and regulatory guidelines.
    Application of 7-Methylisoquinoline

    Applications of 7-Methylisoquinoline in Industrial Manufacturing

    As a direct manufacturer of 7-Methylisoquinoline, we supply this raw material for several specialized industrial sectors. Below, we outline the principal downstream application segments, including precise compliance requirements, usage ratios, integration steps, and the finished goods produced by our clients. All data reflects real industrial practice.

    1. Pharmaceutical Intermediate Synthesis for Antihypertensive Agents

    Our clients in pharmaceutical manufacturing utilize 7-Methylisoquinoline as a crucial intermediate in the synthesis of several second-generation antihypertensive APIs, especially within the class of isoquinoline-derived beta-blockers and vasodilators. Production processes require strict solvent and impurity controls. The raw material undergoes N-alkylation and further condensation to introduce side chains. Site audits and batch records are standard protocol. The downstream processes demand analytical traceability via validated HPLC and GC methods to ensure purity for subsequent transformations in regulated facilities.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as required by FDA 21 CFR Part 210/211
    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP <467> Residual Solvents
    • European Pharmacopoeia (Ph. Eur.) monograph 2.2.46

    Typical usage ratio

    • Range: 0.07–0.12 molar equivalent per downstream API, adjusted based on target yield and impurity profile; excess may be dialed down through real-time reaction monitoring

    Downstream process integration

    • Charged in semi-batch reactors with controlled base addition and phase separation; followed by isolation and purification steps prior to downstream amination or alkylation stages

    Final product types

    • Bulk antihypertensive APIs (e.g., isoquinoline-derived beta-adrenergic blockers)
    • Finished pharmaceutical tablets and injectables supplied under DMF

    2. Agrochemical Active Ingredient Precursor

    Agrochemical manufacturers employ 7-Methylisoquinoline for the targeted synthesis of select pyridoisoquinoline and tetrahydroisoquinoline herbicides and fungicides. This material participates in cyclization and reduction chemistries to form core structures, leveraging its methyl substituent to tailor bioactivity. Quality assurance requires raw material release specifications aligned to downstream activity screens. Only lots meeting low moisture and confirmed polymorphic form proceed to the main condensation stage.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • European Union Regulation (EC) No 1107/2009
    • FAO/WHO Specifications for Plant Protection Products
    • REACH registration for supplied intermediates

    Typical usage ratio

    • 0.10–0.16 molar fraction in target active ingredient synthetic route; varies according to required methyl orientation and crop selectivity demands

    Downstream process integration

    • Introduced during the initial heterocycle assembly stage prior to halogenation or sulfonation; monitored via NMR for conversion and selectivity

    Final product types

    • Technical herbicide and fungicide actives
    • Formulated crop protection products (ECs, SCs, WDGs)

    3. Dye and Pigment Intermediate for High-Performance Pigments

    We supply 7-Methylisoquinoline to pigment producers for use as a key intermediate in constructing high-performance organic pigments—specifically within the isoquinolinequinone class for applications in automotive coatings and industrial inks. The methylisoquinoline core acts as a precursor for selective oxidation and coupling with arylamines or diketones. Quality requirements restrict trace metal and aromatic amine contamination. Reactant homogeneity and purity directly influence chroma stability and dispersibility in the end product.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (for environmental controls)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice
    • EU REACH compliance for industrial chemical intermediates
    • Automotive OEM material certification (e.g., VW standards)

    Typical usage ratio

    • Batch ratio: 0.08–0.14 mole per pigment batch, depending on specific shade and pigment performance requirements

    Downstream process integration

    • Fed during the condensation/coupling step in pigment synthesis; followed by oxidative transformation and controlled crystallization into pigment form

    Final product types

    • Isoquinolinequinone-based pigment concentrates
    • Finished automotive and industrial coatings
    • Specialty printing inks and dispersions

    4. API R&D and Custom Synthesis Platform

    Contract research and manufacturing organizations (CROs and CDMOs) incorporate 7-Methylisoquinoline for rapid structure-activity relationship (SAR) exploration and pilot-scale custom synthesis of isoquinoline-derivative drug candidates. Laboratories demand robust supply chain documentation, CoA traceability, and lot-specific impurity profiling. Usage adapts flexibly to experimental target structure requirements, with aliquoting controlled via weight and molarity for reactions including N-oxidation, C-functionalization, and cross-coupling.

    Industry compliance standards

    • Good Laboratory Practice (GLP) (OECD Guidelines)
    • ISO/IEC 17025 for analytical method validation
    • Material Safety Data requirements (GHS/CLP)
    • Institutional SOPs for new chemical entity (NCE) handling

    Typical usage ratio

    • Small scale: 0.05–0.2 mole per reaction based on project scope; scaling protocols validated per batch with analytical reference material as controls

    Downstream process integration

    • Weighing and dosing during early R&D or first-in-man process steps; integration in parallel synthesis blocks, with documentation of all transfer and handling activities

    Final product types

    • Non-GMP active pharmaceutical ingredient candidates
    • Bench-scale intermediates for SAR libraries
    • Stock solutions for HTS (high-throughput screening)

    5. Organic Electronic Material Synthesis

    Manufacturers in the organic electronics sector use 7-Methylisoquinoline as a synthetic building block in developing charge transport materials for OLEDs and OFETs. The methyl group influences packing and charge mobility in the final oligomer or polymer. Quality controls emphasize batch-to-batch consistency and ultra-low water content. Reactions include direct arylation or Suzuki coupling, and the material often enters nitrogen glovebox lines to prevent oxidation at sensitive synthetic nodes.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for homogenous materials
    • IEC 61249-2-21 for halogen-free content
    • ISO 9001:2015 and ISO 14644 (cleanroom manufacturing environments)
    • Internal client audit requirements

    Typical usage ratio

    • Standard: 0.09–0.13 equiv per coupling unit; ratio adjusted based on target conjugation length or derivative end group density

    Downstream process integration

    • Fed into reaction vessels under inert (argon, nitrogen) conditions; coupled in sequences building up length and branching of conductive or emissive polymers

    Final product types

    • Organic light-emitting diode (OLED) precursor molecules
    • Semiconducting oligomers and small molecules
    • Charge-transport layer components for thin film and display industries
    Free Quote

    Competitive 7-Methylisoquinoline prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Getting to Know 7-Methylisoquinoline From the Manufacturer’s Bench

    A Closer Look at 7-Methylisoquinoline

    Face to face with 7-Methylisoquinoline, you’ll notice the familiar aromatic scent that hints at its backbone in organic synthesis. In the earliest days of synthesizing this compound, we spent long nights optimizing purification, stripping away color bodies and fine-tuning solubility with a craftsman’s patience. Those lessons linger. When a customer asks for low-impurity lots, we recall the heated columns and steady hands behind each lot we dispatch. 7-Methylisoquinoline, CAS 1836-38-6, with the structural formula C10H9N, delivers a pale-to-yellow clear liquid at room temperature when prepared correctly. This isn’t a commodity; it’s a foundation for downstream chemistry and deserves care.

    Model, Specifications, and Purity Assurance

    Batch to batch, we work with a standard that holds its shape under scrutiny: GC purity at or above 98.5% is achievable, and most clients opt for our premium streams, usually above 99%. Quality checks run daily on archived aliquots, with routine moisture determination and residual solvents factored per ICH Q3C guidelines. Meeting analytical marks means less downstream troubleshooting, a point our technical support team stresses with every kilogram we certify.

    In our reactor halls, pressure, load temperature, and hold times are all recorded in real time. Past experience with poorly defined temperature ramps led to measurable shifts in color and yield. We record every deviation in batch records, conscious that trace amounts—be it 1-methyl derivatives or even phthalate contamination—can rear their heads unless you keep a tight operation. No short-cuts. If a batch falls off spec, we reprocess or strip and rerun, even if it slows throughput. Chasing quantity never outweighs the headache of failed downstream reactions caused by off-spec feedstock.

    Our facility handles a variety of methylisoquinoline analogs, and keeping those lines clean protects our integrity. Separate storage and fresh filtration matter. We’ve taken direct calls from medicinal chemists and small molecule innovators who hit snags with cross-contamination from less disciplined suppliers. These teams rely on us knowing the difference between methylated positions. The 7-methyl isomer especially resists confusion with its 6-methyl and 8-methyl cousins under careful analytical scrutiny: retention times, NMR peaks, and reactivity give them away. For discovery programs and patent-critical intermediates, that confidence can make or break a timeline.

    Usage: A Versatile Scaffold in Synthesis

    You find 7-Methylisoquinoline at the crossroads of both academic curiosity and the unforgiving metrics of business-scale synthesis. Teams in pharma research seek it for its role in designing new CNS-active pharmaceuticals. Some experimental anti-infectives and anti-inflammatory projects here and abroad trace their roots to this molecule’s ring system. Medicinal chemists value the methyl at the 7-position for how it modulates electronic properties and metabolic stability. Over years of supplying kilo-scale lots to synthetic and process chemistry labs, we’ve learned that purity isn’t just a QA talking point—it shifts assay reliability, NMR clarity, and reproducibility.

    On the plant floor, our job rarely ends with just shipping drums or flasks. We see 7-Methylisoquinoline feature in library synthesis, pilot campaigns, and at times even GMP routes. From time to time, customers return with tales of chromatographic headaches—ghost peaks hinting at instability or process mishaps. Our support team digs in, troubleshooting with forced degradation and stability data to ensure our material arrives with the promised shelf life, usually at least 24 months in ventilated storage, kept away from direct sunlight and excess moisture. Chemists trying to build more complex structures, such as isoquinoline-bearing heterocycles or functionalized materials for OLED research, also gravitate to our material for low impurity profiles, confident that unexpected reactivity won’t throw off their synthetic plans.

    Comparing 7-Methylisoquinoline With Its Counterparts

    For practitioners used to 2-methyl or 6-methylisoquinolines, the jump to 7-methyl is not a trivial substitution. We see the difference not only in spectral analysis—proton and carbon shifts behave differently—but also in chemical logic. Certain reactions, like directed lithiation or palladium-catalyzed couplings, yield selectivity profiles that only a properly substituted 7-position can deliver. Years spent watching customers optimize reaction routes confirm that even small errors in isomer assignment can derail months of work. Ordering from manufacturers who don’t do exhaustive screening of isomeric purity has led project chemists into cul-de-sacs more often than they’d admit.

    Niche applications in dye chemistry and organic electronics sometimes call for close structural analogs but require the specific physical profile of 7-Methylisoquinoline: melting and boiling point, solubility, and clean aromaticity. Even something as prosaic as odor—yes, long before analytics, noses on our team could peg adulterants above parts per thousand—remains a practical tool for QA. Unlike general traders, we account for trace byproducts from each synthesis stage and keep records open for clients who build regulatory submissions. Transparency doesn’t sell itself; it’s earned batch after batch.

    Some international regulations now assign extra scrutiny to positional isomerism, requiring full characterizations. Our in-house NMR, mass spectrometry, and FTIR systems run the actual crude and purified lots, and we hold retained samples for each production run. Customers with EPA or REACH requirements often need not just a certificate, but proof that a manufacturing process is traceable from raw material to finished drum. We've set up digital traceability in our facility, going beyond paper trails, to anticipate those audits.

    Consistency: The Unspoken Advantage of Direct Manufacture

    We often hear from users burned by variable batches from brokers or traders: inconsistency in color, trace metals, or even degradation during transit. Those failures usually trace back to long supply chains and lack of direct accountability. In our shop, the story changes. Our QA team works unit by unit, and packaging always follows finished product testing—not the other way around. We select inert PE drums or fluoropolymer-lined containers after a major client flagged leachables from substandard packaging years ago. Our own lessons mean customers see less yellowing or pH drift after months in storage. You count on small measures like these to maintain a research program or maintain specs in regulated manufacturing.

    By working directly from raw material procurement—often starting from commercially available phenylethylamines or benzylamines—we guarantee consistency in isomer content. This advantage seems simple until a customer’s route stumbles due to a switch in synthetic origin or residual solvents. Our method balances cost and purity, avoiding unnecessary byproducts. Monitoring every variable, from heat-up rate to cooling protocols, adds hours to a shift, but those hours buy batches that perform as they should.

    Manufacturing consistently means handling both the mundane and unexpected with care. Raw material price spikes, occasional labor issues, or shifts in environmental regulations have all pushed us to refine workflow, retrain operators, and revisit waste handling strategies. Disposing of mother liquors and cleaning out methylated residues gets expensive, but avoiding cross-contamination comes first. We have seen too many stories from labs sabotaged by trace amounts of a wrong isomer or unremoved catalyst. Customers with strong vendor-audit programs focus on actual hands-on practice, not just certificates—visiting in person to watch the lines, review SOPs, and audit documentation.

    Quality Control: Real Challenges, Real Solutions

    There are no shortcuts. Submitting samples for stability studies, running freeze-thaw cycles, and testing against light and air has paid dividends with challenging shipments: we field rare customer complaints about off-odors or color changes by pulling reference samples and running them alongside returns. One batch, air-shipped during a regional heat wave, arrived a shade deeper than expected, and the root cause analysis traced it to a missed desiccant and a carrier mix-up. We took immediate steps—revamped HVAC at the loading dock, doubled packaging checks, added shipment pre-cooling for destinations known for punishing climates. Those aren’t theoretical fixes. They come from recognizing that one-off mishaps matter as much as routine success.

    Trend analysis sometimes spots process drift before it shows up in a customer’s flask. Internal audits look for batch-to-batch yield variation and the rare appearance of side-products. Our logs track instrument calibration and cross-train QC bench teams so instruments never run with questionable baselines. When a batch trips a spec—from a faintly shifted UV max to a surprising trace halogen—we stand behind the material with transparent retesting, offering full refund or rapid resupply. These practices didn’t appear overnight but came from years of problem-solving when single-digit ppm impurities turned out to restrain a whole project.

    Working With Customers: More Than Transactional

    Supply contracts in this field go beyond price per kilo or packaging spec. We have lost and won deals based on how we help users with troubleshooting, custom storage, and shipping requests. Some need smaller quantities for scale-up or route development; others require 200-kilo shipments filled under protective gas and stored double-wrapped to prevent ingress of oxygen or light. Years ago, a research client approached us after encountering oxidative decomposition on a sensitive analogue. We worked side by side to fine-tune the fill and purge cycles, revalidating shelf life. That relationship grew into a longer-term partnership, where ongoing feedback from their analytical team led us to even cleaner isolations and storage protocols improved for everyone.

    We coat every phase of supply with this attitude. Detailed documentation, open lines of communication, and readiness to send technical staff into a customer’s lab for troubleshooting have become the norm. Discussions during vendor audits often extend beyond certificates to process maps, waste streams, and contingency supplies. With regulatory pressures mounting for pharmaceutical and specialty material uses, we arm our clients with whatever batch-specific data they ask for—trace elemental scans, mass spectral fingerprints, detailed NMR spectra—no need to hunt down these resources from third parties or jump between departments.

    Regulatory and Environmental Responsibility

    Compliance with evolving environmental and supply chain regulations raises real questions. Unlike traders or brokers, we source solvents and reagents from audited upstream suppliers, running random spot compliance tests to guard against banned substances. Solvent recycling, emissions control, and waste tracking have become much more than paperwork; inspectors expect detailed logs and traceable signatures at every stage. Occasional disruptions in supply, or even international shipment slowdowns caused by regulatory checks, have shaped how we stock and buffer our key intermediates.

    Operators receive regular safety and handling training, not just because the safety sheets require it, but because decades of chemical manufacturing prove that inattention causes accidents. We realized early that investing in proper containment, scrubbers, and effluent treatment pays both in lower incident rates and less downtime. Selection of raw materials avoids processes that generate known Persistent Organic Pollutants or regulated byproducts. A recent inspection required documentation of not only chemical identity but also evidence for clean water discharge and air stream handling, with real-time emission data. The process gets heavy, but owning the manufacturing chain means every improvement, audit, and inspection passes that value back to both customers and employees.

    Challenges and Ongoing Improvements in Manufacturing

    Chemical manufacturing today does not look like it did even a decade ago. Tighter labor markets, changing regulatory frameworks, and higher expectations for documentation and traceability lead to ever-shifting requirements. Our facilities have pushed through multiple automation upgrades and invested in digital batch tracking. These changes restrict human error, but the old skills—attuned senses, real-time decision making—still count. Manufacturers that ignore process nuances in pursuit of speed or volume risk short cuts that sabotage customer work.

    Integrating new process controls and optimizing yields took years of cumulative experience. We’ve extended in-line analytics, expanded training programs for operators, and share best practices through regular kaizen reviews on the production floor. Not every innovation sticks, but clear data on improved reproducibility, faster troubleshooting, and less need for manual rework proves the worth of a manufacturing-led system.

    Staying ahead means dedicating resources to process validation, ongoing impurity trend analysis, and planned upgrades to waste management systems. Every international shipment or customer complaint turns into a learning moment, prompting reviews and protocol changes that build trust batch by batch.

    Looking Ahead: Building Confidence Through Manufacturing Expertise

    7-Methylisoquinoline will keep evolving in its range of uses, from pharma intermediates to next-generation materials. This journey—built on practical knowledge, process transparency, and an almost stubborn refusal to compromise—anchors what we do now and shapes what comes next. We don’t take shortcuts, because the chemists, process engineers, and innovators who rely on our product can’t afford uncertainty. Direct contact with our customers, deep familiarity with our process, and open documentation mean orders arrive exactly as requested. Our work doesn’t always make headlines, but it keeps the foundation solid for those translating molecules to medicines and materials.

    Manufacturing 7-Methylisoquinoline is as much about discipline as it is about chemistry. Every kilogram shipped reflects not just technical expertise, but a commitment to those who depend on our work being right the first time—every time. That’s the standard we set, and the standard our clients have come to expect.