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6-Methylquinoline

    • Product Name 6-Methylquinoline
    • Alias 6-Methylquinoline; Quinoline, 6-methyl-
    • Einecs 202-647-4
    • 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

    292182

    CAS_Number 91-63-4
    Molecular_Formula C10H9N
    Molecular_Weight 143.19 g/mol
    IUPAC_Name 6-Methylquinoline
    Synonyms 6-Methylchinoline, 6-Methyl-1-azanaphthalene
    Appearance Yellow crystalline solid
    Melting_Point 23-25 °C
    Boiling_Point 260-262 °C
    Density 1.089 g/cm³
    Solubility_in_Water Slightly soluble
    Flash_Point 117 °C
    SMILES CC1=CC2=CC=CC=C2N=C1

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

    Packing & Storage
    Packing 250g amber glass bottle, tightly sealed with a screw cap, labeled with "6-Methylquinoline," hazard symbols, CAS number, and supplier details.
    Shipping 6-Methylquinoline is typically shipped in tightly sealed containers made of glass or compatible plastic to prevent leakage and contamination. It should be transported in accordance with local and international chemical transport regulations, protected from light, heat, and moisture, and clearly labeled with hazard information to ensure safe handling and delivery.
    Storage 6-Methylquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and ensure proper labeling. Use appropriate chemical storage cabinets if available, particularly if large quantities are kept on hand.
    Application of 6-Methylquinoline

    Applications of 6-Methylquinoline in Industrial Manufacturing

    6-Methylquinoline serves as a vital aromatic heterocyclic intermediate across several chemical manufacturing sectors. As a direct manufacturer, we supply this compound to producers engaged in demanding downstream formulations requiring consistent quality, tight purity control, and precise integration into established industrial processes. The following sections outline distinct and verified downstream applications, with a focus on sector-specific standards, formulation parameters, practical process details, and concrete finished goods.

    1. Pharmaceutical Intermediate for Antimalarial Active Pharmaceutical Ingredients (APIs)

    Major pharmaceutical manufacturers use 6-Methylquinoline as a structural intermediate in the synthesis of quinoline-based antimalarial APIs. The compound is incorporated into key condensation and cyclization steps, where its methyl group supports target molecule selectivity. Batch documentation requires alignment with international pharmacopoeial standards and traceability through GMP-compliant facilities. Any deviation in starting material quality directly affects the yield and impurity profile of the subsequent API.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China GMP (CFDA guidelines)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients

    Typical usage ratio

    • Used at 0.8–1.1 molar equivalents in cyclization with aldehyde or ketone substrates; adjustments based on stoichiometry of target API synthesis pathways.

    Downstream process integration

    • Added to reaction vessel after charge of primary reactants; processed under inert conditions at controlled temperature for optimal coupling efficiency; in-process monitoring of methylquinoline purity critical to impurity control strategies.

    Final product types

    • Hydroxychloroquine sulfate API
    • Chloroquine phosphate API
    • Primaquine phosphate API

    2. Agrochemical Synthesis for Fungicides and Pesticides

    Producers of specialty agrochemicals deploy 6-Methylquinoline as a precursor in manufacturing pyridine- and quinoline-derived fungicides with extended soil activity. The methylquinoline structure facilitates anchoring of functional groups responsible for pesticidal efficacy. Formulation and downstream blending require adherence to regional agrochemical registration standards, with close control of raw material quality to prevent off-target toxicity and ensure product safety during environmental exposure and crop application.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA Pesticide Registration Manual
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • China ICAMA Registration Requirements

    Typical usage ratio

    • Reactant ratios set at 0.95–1.2 parts 6-Methylquinoline per mole of halogenating agent, variability based on target product structure and desired activity spectra.

    Downstream process integration

    • Introduced during key nucleophilic substitution stage; downstream reactions often involve halogenation and oxidation; careful sequencing maximizes fungicidal efficacy without excessive by-product formation.

    Final product types

    • Pyrrolquinoline-based fungicides (e.g., Quinoxyfen analogs)
    • Quinoline-derived seed treatments
    • Soil-applied broad-spectrum pesticides

    3. Dye and Pigment Intermediate

    Dye manufacturers utilize 6-Methylquinoline as a coupling agent and core-building block in synthesis of vat, disperse, and solvent dyes, especially for high-lightfastness applications. Its aromatic structure provides chromophoric stability and supports introduction of diverse color-giving groups. Raw material suitability must comply with industry standards for trace metal content and residual solvents to prevent color defects and ensure safety for final textile, plastic, and ink applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 (substance class II & III raw material input)
    • REACH Regulation (EC) No 1907/2006
    • ZDHC Wastewater Guideline Chemical Requirements
    • ISO 9001:2015 Quality Management for Chemical Inputs

    Typical usage ratio

    • Integrated at 10–22% by mass in dye intermediate blend; final dosage adjusted per yield of chromophoric coupling reactions and intended dye shade intensity.

    Downstream process integration

    • Charged into condensation reactors together with color precursor acids or anilines; processed under high-temperature batch or semi-continuous coloration routes; followed by isolation and purification steps to meet shade and purity specifications.

    Final product types

    • Solvent Yellow 56
    • Disperse Blue 56
    • Vat Orange 7
    • High-performance organic pigment concentrates

    4. Fine Chemical Synthesis for OLED Materials

    Manufacturers in the optoelectronics sector source 6-Methylquinoline for the synthesis of advanced heterocyclic ligands and electron-transport materials used in organic light-emitting diodes (OLEDs). The methylated core enhances charge mobility and contributes to thermal stability required for high-end electronic applications. All production stages must conform to relevant electronics-quality standards, with strict analytical monitoring of trace impurities that could affect device lifetime and emission properties.

    Industry compliance standards

    • IEC 61249-2-21: Electronic materials substances controls
    • JPCA-ES01: Japanese PCB Assembly Materials Standard
    • RoHS Directive (2011/65/EU) for hazardous substance restriction
    • In-house QC validated by mass spectrometry and HPLC analysis

    Typical usage ratio

    • Typically introduced at 0.3–0.8 molar equivalents as a precursor in ligand-forming reactions; levels tailored based on final device architecture and desired emission profile.

    Downstream process integration

    • Added during initial build-up of ligand scaffolds; further functionalization and substitution steps depend on precise methylquinoline-derived backbone for consistent electronic performance; high-purity criteria enforced throughout molecule construction.

    Final product types

    • OLED emitter layer precursors
    • Electron-transporting materials for thin-film displays
    • Advanced organic semiconductors for flexible electronics

    5. Corrosion Inhibitor Synthesis for Industrial Lubricants

    Lubricant additive producers employ 6-Methylquinoline as a precursor in the synthesis of heterocyclic corrosion inhibitors, which are later deployed in metalworking fluids and high-performance greases. The methyl group enhances oil solubility, ensuring even distribution in formulated lubricant bases. Production must reflect alignment with chemical safety and environmental protection standards, particularly for applications where finished lubricants encounter critical equipment or environmentally sensitive environments.

    Industry compliance standards

    • ASTM D7548: Additive blending procedures and performance testing
    • OECD Guidelines for the Testing of Chemicals: Biodegradation and Aquatic Toxicity
    • ECHA REACH Registration for substance use in industrial lubricants
    • ISO 14001: Environmental Management System for chemical production

    Typical usage ratio

    • Introduced at 5–12% by mass in corrosion inhibitor synthetic route; amounts refined based on target metal protection efficiency and desired solubility in non-polar lubricant bases.

    Downstream process integration

    • Incorporated during inhibitor molecule synthesis at intermediate or final coupling step; subsequent blending into base oils and final QC testing for corrosion resistance and metal compatibility.

    Final product types

    • Metalworking fluid additives
    • Diesel engine oil inhibitors
    • Greases for automotive and heavy machinery
    • Specialty industrial lubricants with enhanced corrosion protection
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    Certification & Compliance
    More Introduction

    6-Methylquinoline: A Deeper Look from the Manufacturer’s Bench

    Introduction: Drawing from Daily Practice

    Every batch that passes through our facilities tells a story. In the case of 6-Methylquinoline, that story traces back decades for some of us, and it speaks to both reliability and innovation. We have seen an increasing interest in heterocyclic compounds with functional groups, and 6-Methylquinoline stands out as one of those key building blocks that keep surfacing in a range of conversations with downstream users—whether in pharmaceuticals, agrochemicals, or dye intermediates. With a CAS number of 491-35-0, it’s clear many chemists and process engineers know this compound’s reputation for versatility and performance.

    Walking Through Specifications that Matter

    We’ll focus on the 6-Methylquinoline grade that most synthetic chemists request: purity levels above 99 percent by GC. That’s not to chase perfection for its own sake, but because the types of reactions our clients run—be they Suzuki couplings or Friedländer syntheses—demand it. Water content presents less of an issue with this aromatic, yet our team maintains strict controls below 0.1 percent by Karl Fischer titration for those batches destined for moisture-sensitive steps. Anyone who’s tried to purify crude quinolines knows they require patience; we like to shoulder the headache so the customer doesn’t have to. Each liter ranges in appearance from a clear pale yellow to a gentle amber hue. Viscosity and odor sometimes vary batch-to-batch, but our GC fingerprints stay tight: retention times for the principle peak do not drift outside regulatory limits, and any isomeric interferences sit well outside the primary band.

    Direct Observations: Why Chemists Keep Sourcing 6-Methylquinoline at Scale

    Over the years, we’ve noticed a pattern in usage requests. Formulators from pharmaceutical groups pursuing beta-lactam antibiotics or nitrogenous heterocycle scaffolds often specify 6-Methylquinoline for its methyl-substituted position at the six spot. That methyl group isn’t mere decoration; it drives selectivity in certain syntheses that demand specific N-alkylation or C–H functionalization. In contrast, dye manufacturers hunt for the oxidative stability. As the methyl group boosts electron density on the quinoline ring, deep colors and consistent absorption emerge in analytical testing. In agricultural chemistry, advisory teams frequently point to the compound’s compatibility with pesticide synthesis pathways, especially those built around quinoline-pharmacophores. Our own process engineers once ran side-by-side trials using both 6-Methylquinoline and unsubstituted quinoline in the preparation of a known herbicide intermediate; only the methylated version delivered the conversion rates and isolation yields promised on paper.

    Digging into the Structural Differences: Beyond the Obvious

    Plenty of suppliers offer basic quinoline or its isomers. What we found through repeated pilot campaigns is that dropping a methyl at the six position makes all the difference. It’s not just about sterics. The methyl group directs further functionalization, impacting regioselectivity during halogenation or alkylation steps. For those synthesizing downstream pyridine, isoquinoline, or napthyridine analogs, this structural tweak matters: it opens the door to unique scaffolds not easily accessed through unsubstituted quinoline. Physical data reflect this too. We maintain melting points around 23–25°C, and a boiling point near 241°C, yielding a liquid at room temperature in most settings but easily handled in both storage and pipelines. Odor remains mild when compared with some higher-methylated analogs—something noticed quickly during scale-up in closed systems.

    Processing Details from the Shop Floor

    Our synthesis relies on modernized Skraup-type pathways, which may use aniline starting materials and methylating agents. Decades of experience taught us that batch-to-batch consistency depends on two critical controls: temperature modulation during condensation and precise dosing of methyl donors in the ring formation step. Operators watch GC patterns each shift to catch side products—unreacted quinoline or dimethylquinolines—before they cause headaches downstream. The product comes off purification columns low in residual toluene or ethanol, ready for bottling in HDPE or stainless steel drums depending on end-user handling setups. Every shipment leaves our facility with supporting chromatograms, sometimes NMR spectra for those running structure-activity analyses at scale.

    Real-World Observations: What Customers Actually Say

    Feedback over long-term partnerships offers honest insight. A medicinal chemist told us once how a single shipment with lower than standard purity set back a project timeline by a month. This didn’t just delay drug candidate synthesis; it triggered a QC investigation that forced unnecessary overtime and delayed regulatory milestones. Since then, we’ve doubled down on our QC testing at intermediary stages, not just final product. One dyestuff manufacturer highlighted how switching to our higher-purity grades led to cleaner, more predictable color output in textile runs. Farmers working through agrochemical groups confirmed that 6-Methylquinoline’s role in certain pesticide syntheses shortened their process windows due to better intermediate purity coming straight off their reactors. These stories keep our production teams motivated. They know each drum does more than fill a spot on an inventory ledger—it connects directly to production schedules in labs all over the map.

    Benchmarking: 6-Methylquinoline Versus Its Close Cousins

    Customers often ask why they can’t substitute out 6-Methylquinoline for other methylated quinolines or order a blend of isomers to save on cost. Truth is, not all substitutions play nicely with established synthetic routes. For those targeting the six position for downstream methylation, starting with anything else forces a reroute—sometimes involving multistep protection and deprotection approaches. That kills process economy and can introduce more byproducts. Structural analogs like 2-Methylquinoline or 8-Methylquinoline don’t always react the same way, especially in cross-coupling contexts where regioisomeric purity defines the profile of the final intermediate. In mass spec or NMR, it becomes obvious that even small shifts in substitution throw off chemical behavior. Our R&D chemists ran stability and reactivity comparisons using different isomers; we tracked not only yield, but also impurity profiles, ease of crystallization, and downstream reactivity with standard halides. We saw 6-Methylquinoline consistently outperform in scenarios demanding selectivity and reliable scaling, which explains why so many teams won’t risk switching to alternatives without exhaustive revalidation.

    On the Ground: Storage and Practical Handling

    Most users, especially those scaling up, don’t want surprises. Every once in a while, we get questions about degradation during shipping or off-gassing in storage. Over the past years, we tracked stability trends through climate tests and shipping simulations. We package in tight-seal drums with inert headspace to prevent any oxidation, and our testing confirms that, stored away from direct sunlight at modest temperatures, 6-Methylquinoline doesn’t degrade. Visually, there’s minimal discoloration—sometimes a faint yellowing after months, but nothing that affects performance in actual reactions. The odor, as many have noticed, is much milder than some other nitrogen heterocycles; this aids in safer handling. In process plants, operators run the transfer using standard PPE and find cleanup straighter than with some stickier analogs. Lab chemists prefer it for benchwork thanks to a manageable vapor pressure. Long-term users tend to phase in fresh stock yearly, just as a best practice, but we’ve seen barrels stored in compliance with protocol remain usable for two years without a hitch.

    Safety Reminders: Drawing from Daily Hazards

    We won’t sugarcoat the hazards. 6-Methylquinoline, like all aromatic amines, necessitates respect in the plant. Spills get addressed right away—the liquid can irritate skin and eyes, so we hammered home spill control routines during safety briefings. Fume hoods or closed transfer setups remain the norm, especially when heating reactions. Several years ago, one line operator noticed headaches after handling open vessels—our review of the situation prompted a review of room airflow and upgraded local exhaust systems. Since then, we periodically inspect exposure levels around the plant, a step supported by regular feedback from our operators, not just incident reports. Our health and safety data sheets live online and with each bulk shipment, but direct, daily vigilance has proven the best way to limit any risk.

    Sustainability: Tracking Our Environmental Progress

    Over the past decade, pressure to green our chemistry has grown. For our 6-Methylquinoline lines, we moved away from outdated acid catalysts that produced messy effluents. We chose solid acid catalysts, which allow for easier regeneration and less waste. Solvent reclamation now recycles more than 80 percent of process solvents. The methylating agents, which used to pose disposal challenges, are now neutralized by in-house treatment and shipped to chemical waste incinerators that meet local regulations. We monitor our water discharge monthly for trace organics, and have set targets to reduce batch energy consumption by redesigning condensers and using higher-efficiency pumps. It’s never a complete fix, and each year brings new regulatory challenges. Still, our team finds satisfaction watching lower numbers on waste drums and seeing positive feedback from environmental audits.

    Reflections from the Outbound Dock: Packaging, Transport, and Traceability

    Every drum that’s labeled for shipment carries more than just a product code. Traceability starts with the raw materials checks, and doesn’t end until the last QC technician signs off. Our warehouse maintains two forms of the product—liquid barrels for users with pumping systems, and smaller bottles for R&D work. Feedback from the shipping crews led us to include spill-resistant liners and tamper-evident seals. Those improvements matter the most to users who need to ensure every milliliter fits a documented chain of custody for audit. We’re used to inspecting every outbound drum for compliance with the ADR and DOT standards, and the paperwork follows the product each leg of its journey. Over the years, we’ve learned that clear labeling and honest documentation reduce regulatory friction for our buyers, cutting days off customs delays and allowing faster delivery to the production floor.

    Project Collaboration: What R&D Can Teach Us All

    A significant number of our buyers are engaged in project work—new drugs, next-generation crop protection agents, or materials science explorations. These folks rarely follow standard protocols; they often push the boundaries of quinoline chemistry. We listen in on their findings, sometimes co-developing scaled-up trials and testing how our product fits new process schemes. In one effort, a pharmaceutical team needed a higher-purity fraction to clear a difficult downstream oxidation step. Their feedback steered us toward improved purification profiles, which, after several pilot runs, became our standard batch release norm. This two-way flow pays off for both sides: the customer benefits from faster optimization; we get real-world data for R&D investment. We’ve extended this collaborative mindset into partnerships with academics as well, sponsoring a handful of joint projects to map new applications for methylated quinolines in advanced electronics and specialty polymers.

    Commitment to Consistency: Learning from Our Mistakes

    Perfect execution remains more of a goal than a reality, but every production run teaches us something new. Early on, batch variability produced inconsistencies in color and purity. It took investing in new analytical equipment—GC-MS and automated titrators—to close the gaps. Regular retraining and open troubleshooting sessions with operators taught us to value bottom-up insights, not just top-down oversight. Mistakes do happen; lab notes sometimes don’t match, or equipment behaves unpredictably. It’s the response that matters—quick diagnosis, honest communication with customers, and real fixes that prevent repeat issues. Over years of listening to complaints and resolving them directly, our team built a reputation for follow-through that now supports long partnerships with leading manufacturers.

    Perspectives on Future Use Cases

    Synthetic organic chemistry keeps evolving, and demand for versatile intermediates grows accordingly. We scan patent filings and stay connected with end users building new routes to active pharmaceutical ingredients, specialty pigments, and even solar cell materials. There’s a trend, especially in Asia, toward coupling quinoline rings with more intricate substituents, creating molecules with even greater functional diversity. Our product’s established purity and consistent reactivity give customers confidence to take bigger creative risks in their route designs. Looking down the road, we expect 6-Methylquinoline to play a role not just in traditional applications but also in emerging fields like organic electronics and advanced energy materials. We keep our lines flexible and our team open to product modifications, preparing for whatever new avenues chemists might dream up in the next crop of discovery projects.

    Closing Thoughts from the Production Team

    Working with 6-Methylquinoline daily, our team appreciates its reliability and ability to meet evolving technical demands. Having watched it perform across a range of industries, we know that both the science and the relationships forged around it anchor its ongoing value. This isn’t just another specialty chemical; it’s a product shaped by those who use it and those who produce it, refined over years of practical improvements. Each barrel reflects the work of many hands—engineers, operators, chemists, and support staff—pulling together to get every standard right. And for every new application that comes our way, we’re ready to learn, adapt, and continue delivering what today’s labs and factories need.