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5-Aminoquinaldine

    • Product Name 5-Aminoquinaldine
    • Alias 5-Amino-2-methylquinoline
    • Einecs 210-279-6
    • 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

    596041

    Cas Number 670-94-0
    Molecular Formula C10H10N2
    Molecular Weight 158.20 g/mol
    Iupac Name 5-amino-2-methylquinoline
    Appearance Light brown to beige solid
    Melting Point 60-64°C
    Boiling Point 337.8°C at 760 mmHg
    Density 1.17 g/cm³
    Solubility In Water Slightly soluble
    Synonyms 2-Methylquinolin-5-amine

    As an accredited 5-Aminoquinaldine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Aminoquinaldine is packaged in a 25-gram amber glass bottle with a tamper-evident cap, labeled with safety and handling instructions.
    Shipping 5-Aminoquinaldine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packages must comply with national and international regulations for hazardous materials. Proper labeling and documentation are required. It should be handled and transported by trained personnel to ensure safety and prevent accidental release during shipping.
    Storage 5-Aminoquinaldine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture, heat, and direct sunlight. Ensure proper labeling and access is limited to trained personnel. Store in accordance with local regulations and chemical safety guidelines to prevent contamination and degradation.
    Application of 5-Aminoquinaldine

    Applications of 5-Aminoquinaldine in Industrial Manufacturing

    5-Aminoquinaldine serves as a specialized chemical building block for several sectors, most notably pharmaceutical synthesis, dye intermediates, agrochemical manufacturing, organic electronic materials, and specialty heterocyclic compound production. Its use in downstream processes depends on precise industry regulation, batch-specific dosage adjustment, and integration into demanding multi-step reactions required by industrial manufacturers.

    1. Pharmaceutical Intermediate for Antimalarial Drug Synthesis

    Pharmaceutical manufacturers use 5-aminoquinaldine as a crucial intermediate in the targeted production of active pharmaceutical ingredients (APIs) such as chloroquine analogues and related antimalarial drugs. Its role requires strict raw material traceability, validated synthetic processes, and adherence to international pharmacopeia specifications. The compound enters reaction schemes for quinoline derivative APIs through N-alkylation or acylation, followed by ring closure and final crystallization, serving as a determinant of product yield and purity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters on Starting Materials
    • European Pharmacopeia (Ph. Eur.) Monographs on Pharmaceutical Substances
    • FDA 21 CFR Part 211 cGMP

    Typical usage ratio

    • 20–35% molar basis as limiting reagent in quinoline API synthesis, fine-tuned by product target and process yield analysis

    Downstream process integration

    • Introduced in Stage 2 as the quinoline ring amination/blocking agent, pre-purification
    • Participates in subsequent N-substitution, acylation or condensation steps
    • Subjected to mother liquor recovery post-reaction to minimize loss
    • Monitored for residuals in final API QC by HPLC and LC-MS

    Final product types

    • Chloroquine phosphate
    • Amodiaquine hydrochloride
    • Other 4-aminoquinoline APIs
    • Bulk antimalarial intermediates for formulation houses

    2. Intermediate for Azo and Anthraquinone Dyes

    Dye manufacturers select 5-aminoquinaldine as a specialized precursor for formulating intense colorants used in textile, paper, and synthetic fiber applications. The aminoquinoline core supports chemical modification via diazotization and coupling, yielding stable chromophore frameworks. Controlled ratios allow the formation of high-purity pigments meeting end-use fastness, migration, and ecological demands.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile safety)
    • REACH Annex XVII: Dye substance restriction
    • ZDHC MRSL (Manufacturing Restricted Substances List) for effluent safety
    • DIN EN ISO 105 (textile color fastness series)

    Typical usage ratio

    • 10–25% by molecular weight as diazotizable component; ratio refined based on target shade and coupling partners

    Downstream process integration

    • Undergoes initial diazotization in aqueous inorganic acid solutions
    • Couples with aromatic amine or phenolic partners to create target azo or anthraquinone structures
    • Pigment purification via filtration, salt-out, and drying
    • Small molecule impurities monitored by UV-Vis and GC-MS

    Final product types

    • Metal complex azo dyes for wool and nylon
    • Anthraquinone-based disperse dyes for PET fibers
    • High-performance pigments for plastics
    • Specialty colorants for inkjet formulations

    3. Precursor in Agrochemical Active Ingredient Manufacturing

    Chemical processors leverage 5-aminoquinaldine in the synthesis of selective herbicides and growth regulators that utilize quinoline scaffolds. It enables the cost-competitive manufacture of actives with strict impurity control. Downstream agrochemical synthesis involves alkylation, ring substitution, and subsequent formulation into water-dispersible granules or emulsifiable concentrates. Manufacturers carry out quality audits to ensure compliance down to trace levels of aromatic amines.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems
    • China GB 2763 Maximum Residue Limits (MRLs) in food
    • GLP (Good Laboratory Practice) for active ingredient batch documentation

    Typical usage ratio

    • 8–18% w/w as a core intermediate in the active ingredient section, adjusted for target molecule and yield optimization

    Downstream process integration

    • Implemented after initial ring construction, serving as the amino donor for specific quinoline structures
    • Follows with halogenation, chain extension or esterification
    • Final actives blended with surfactants and stabilizers before packaging
    • GC and LC analysis for detection of residual reactants

    Final product types

    • Quinoline-based herbicide technical concentrates
    • Pre-emergent weed control formulations
    • Regulatory-compliant crop protection actives
    • Pesticide premixes for oilseed and vegetable applications

    4. API Intermediate in Veterinary Drug Production

    5-aminoquinaldine finds use in the veterinary sector for the synthesis of API intermediates for animal antiprotozoals and coccidiostats. Compliance with veterinary drug monographs and GMP certification underpins material selection. Manufacturers prioritize lot-specific assays and impurity profiling, with most production destined for conversion into hydrochloride or sulfate finished APIs for premix or injectable veterinary preparations.

    Industry compliance standards

    • VICH GL10 GMP for Veterinary Pharmaceutical Ingredients
    • Ph. Eur. 9.0 Veterinary Substance Monographs
    • US FDA CVM Guidance for Industry #235 (Animal Drug GMP)
    • China Veterinary Pharmacopoeia

    Typical usage ratio

    • 18–30% molar basis as a key step intermediate, ratio calibrated according to animal treatment dose targets

    Downstream process integration

    • Added to multi-step synthetic schemes post-initial ring formation
    • Undergoes conversion to hydrochloride or sulfate salt before final purification
    • Monitored by batch release QC for residual solvents and heavy metals
    • Subjected to advanced impurity mapping using HPLC-UV and ICP-OES

    Final product types

    • Coccidiostat bulk APIs
    • Animal antiprotozoal premix API bases
    • Water-soluble veterinary drug concentrates
    • Injectable veterinary pharmaceutical formulations

    5. Heterocyclic Building Block for Organic Electronic Materials

    In the field of organic electronics, materials engineers employ 5-aminoquinaldine as a heterocyclic scaffold for synthesizing charge transport materials and light-emitting compounds. Entry into polymerization or coupling reactions demands purity exceeding 99.5%, confirmed by NMR and HPLC. Downstream processes require stringent controls for trace metal and halogen impurities to preserve device performance.

    Industry compliance standards

    • IEC 62899-202 Electronic Print Functional Materials
    • RoHS 2011/65/EU for hazardous substances restriction
    • IPC-4101/123 Printed Circuit Base Materials
    • ISO 14001 Environmental Management for Electronic Materials

    Typical usage ratio

    • 5–12% w/w as a monomer or ligand precursor; adjusted per batch by molecular weight targets in pilot-scale polymer production

    Downstream process integration

    • Incorporated at the precursor stage for charge-transport material synthesis
    • Links to aryl or vinyl moieties via C-N or C-C coupling
    • Purified intermediates enter further polymerization or spin-coating steps
    • Final QC by GPC for molecular weight distribution and spectroscopic purity

    Final product types

    • OLED intermediate compounds
    • Organic photoconductors
    • Charge transport materials for LCD backplanes
    • Conductive polymer additives for flexible electronics
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    Certification & Compliance
    More Introduction

    5-Aminoquinaldine: Core Ingredient for Smart Synthesis

    Understanding 5-Aminoquinaldine

    Looking at our daily work inside the plant, 5-aminoquinaldine shows up as a reliable compound that's hard to ignore. This molecule holds a unique place in our line because it offers both versatility and consistency batch after batch. Chemically, 5-aminoquinaldine—known by its IUPAC name 5-amino-2-methylquinoline—adopts the structure C10H10N2, which makes it a member of the quinoline family. That methyl group at the 2-position isn’t just for show; it sets this molecule apart from other aminoquinolines, letting researchers and chemical processors push their syntheses in directions that pure quinaldine or generic quinolines simply won’t go.

    From the earliest days at our facility, we noticed that users appreciate not just the availability, but the reliability of the product’s quality. Our teams dial in the manufacturing conditions, adjusting solvent ratios, temperature settings, and isolation techniques to deliver a crystalline material that chemists can trust. Consistent purity—with typical lots reaching 98% or above—means fewer headaches during downstream reactions, whether someone’s building heterocycles or scouting leads in medicinal chemistry.

    Specifications That Matter in the Lab

    Our typical model of 5-aminoquinaldine arrives as a faintly yellow crystalline solid. The melting point lands around 80–84°C; we control for this with repeated checks, since out-of-range material signals potential impurities. When we prepare each lot, high-performance liquid chromatography and NMR scrutiny back up our purity claims. Moisture and residual solvent content remain minimal thanks to careful vacuum drying steps. Particle size and flowability might sound trivial, but neither researchers nor large-scale processors want to wrestle with lumps or inconsistent dosing. We grind and sieve our batches to let the product pour smoothly and disperse easily, with negligible static or dust.

    Some might ask how our material compares with cheaper, off-brand sources. We’ve tested competitive samples in-house—batch yield, reaction times, and impurity formation tell the story better than any sales pitch. With high-purity 5-aminoquinaldine, side reactions fall away and color remains under control throughout the process. This ends up mattering in real-world synthesis work, where cleaning up tars or repeated re-purifications drain both time and patience. In the pharmaceutical pilot plant, every day spent coaxing a stubborn intermediate through the next step costs real money. Dirty feedstock only compounds the burden.

    Real-World Uses: Not Just a Catalog Entry

    We’ve assisted labs working in areas from dye development to pharmaceutical research. In the fine chemical sector, 5-aminoquinaldine plays a core role in constructing novel heterocycles, azabenzimidazoles, and more. It serves as a building block in anti-microbial, anti-malarial, and oncology efforts because its skeleton can accept a wide range of functional modifications. Academic groups choose it when they need a core that tolerates both electrophilic and nucleophilic substitution, especially where steric flexibility is key.

    A recurring request has come from API route scouting projects—here, our 5-aminoquinaldine starts as a coupling partner or cyclization handle. The amine group at the 5-position faces less competition from ring deactivation, opening up versatile reaction sites for Suzuki, Buchwald, or Ullmann couplings. The methyl at the 2-position impacts regioselectivity in downstream alkylation and acylation, reducing unwanted by-products. These traits give process chemists greater control and higher yields as they push for kilogram or metric-ton outputs.

    We’ve seen the same advantages pop up in dye and pigment research. The structure introduces photophysical properties that chemists need for lightfastness and color stability. Where alternative starting materials bring in trouble during purification, 5-aminoquinaldine’s clean crystallization lessens the post-processing workload. This is particularly relevant for large-scale pigment syntheses, where fighting off trace impurities and finding that razor-thin margin between cost and quality makes or breaks a product line.

    How It Stands Apart from Other Quinoline Derivatives

    A lot of labs start with broader quinoline derivatives, hoping to retrofit them for more targeted chemistry. We’ve run enough side-by-side comparisons to see how 5-aminoquinaldine earns its keep. Compared to unsubstituted 8-aminoquinoline or 3-aminoquinoline, the 5-position variant demonstrates distinctly different reactivity under standard conditions. Electron distribution around the ring changes when a methyl group rides at the 2-position. This subtle twist in electronics enables selective transformations that don’t work cleanly with other quinolines, making it possible to introduce complex substituents for structure-activity studies.

    Another key difference from standard quinaldine is its dual-functionality. While quinaldine and methylquinoline serve as inert scaffolds for further functionalization, 5-aminoquinaldine charts a dual path: retaining the electron-rich amine for nucleophilic steps and the methyl as a steric director. These properties open up diversification tactics that speed up lead optimization, especially when projects jump from gram scale to multi-kilogram campaigns.

    We’ve found that process engineers appreciate more controllable behavior during hydrogenation and oxidation steps. By having both an amine and a methyl anchoring the ring, our compound dodges some of the side reactions that frustrate scale-up. Less reactivity at remote ring positions means fewer chances for by-products or troublesome tars to form in the reactor. You can run reactions hotter, or with more aggressive reagents, without watching your product degrade.

    From a formulation angle, this derivative introduces fewer odor and storage concerns than some close relatives in the same family. With proper handling, it resists oxidation and yellowing that plague more sensitive polyamines. The physical profile—solid at ambient conditions, with low volatility—makes it compatible with both automated and manual dispensing, whether in R&D suites or full-scale manufacturing towers.

    Why Quality in 5-Aminoquinaldine Matters Beyond the Numbers

    Down on the supply floor, quality assurance doesn’t end at a certificate of analysis or batch number. Our workflow takes into account what customers face once they open the drum: ease of re-dissolving, reproducible yields, and predictable performance. Each processing step tracks back to in-process sampling, so if a single run starts to drift, we quarantine the entire lot for further checks. On more than one occasion, this kind of vigilance saved major research programs from derailing.

    Even seasoned chemists feel the pain of inconsistent starting materials. In one pharmaceutical project, a customer struggled with fluctuating impurity profiles and time-consuming column purifications—until they switched over to our 5-aminoquinaldine. Overnight, the burden of troubleshooting dropped, letting the team focus on optimizing their process rather than hunting for hidden contaminants. This kind of direct impact flows back up the supply chain, with smoother tech transfer and less post-synthesis rework.

    Regulatory demands keep tightening year by year. While some sources take shortcuts, our plant puts every lot through both internal and third-party audits. This traceability ensures clean compliance with GMP or REACH requirements for intermediates. Any residue of heavy metals, solvents, or trace amines is flagged and either rejected or reworked. By holding purity and identity to higher standards, we protect not just our reputation, but our downstream partners who rely on a rock-solid chain of custody.

    What It Takes to Produce 5-Aminoquinaldine at Scale

    From a manufacturing standpoint, this compound presents its own challenges. The synthetic route starts with quinaldine, which most know as a tar-like substance prone to side reactions. Selective nitration to give the 5-nitro group, followed by careful reduction, sets the stage. We’ve invested in reactors, environmental controls, and downstream scrubbers tailored just for this product, since nitrogroup reduction can cut corners unless staff monitor pressure and pH every hour.

    Our plant engineers work with safety teams to keep emissions under strict control. Waste streams from nitro reductions and acid washes get neutralized and pre-treated before any disposal. Trained operators oversee both batch and continuous processing, always adapting their protocols to seasonal temperature shifts and variable feedstock quality. Because reproducibility begins on the production floor, we regularly recalibrate and run test batches using customer feedback to inform incremental improvements.

    In terms of final product handling, we store and package 5-aminoquinaldine in lined drums or PE containers that block out moisture and air. Clients handling this material in bulk get support documentation on storage, decanting, and cleaning tips based on our own experience. Accidental contamination in storage bins or transfer lines can threaten the whole batch, so our teams cycle through frequent checks and offer direct support if technical issues arise.

    Supporting Diverse Applications with a Single Product

    End-users aren’t just academic researchers. Coupling agents, small-molecule API intermediates, metal-complex dyes, and specialty resins all draw from the same lot of 5-aminoquinaldine. Scale-up teams appreciate that, due to its moderate melting point and solubility in polar organics, this molecule slides easily into liquid-phase and solid-phase reactions without fuss. We ship to customers who run reactions from room temperature right up to 180°C, often without needing extensive re-optimization.

    Clients in the polymer sector look for amine-functionalized building blocks that avoid excessive crosslinking or branching. Here, 5-aminoquinaldine offers predictable outcomes, allowing users to tailor physical and chemical properties of their resins. Whether forging epoxy intermediates or specialty adhesives, they count on each shipment to perform identically to the last. This consistency stems from how our plant manages trace contaminants—every fraction of a percent matters in sensitive formulations.

    For electronic and sensor applications, customers demand starting materials without trace metals or halogens. Before we send each drum out the door, purification steps cut residual metals below 10 ppm, allowing users to proceed with confidence. The result: cleaner data, sharper reproducibility, fewer failed batches. These assurances support not just bench chemists but quality assurance technicians, regulatory affairs officers, and even technical sales teams.

    Feedback That Shapes Our Manufacturing

    Our ties to the community run deep; chemists and engineers don’t just order a product—they call with direct feedback. Some point to specific issues: filtration clogs, solubility quirks, or trace color changes. Others share success stories, explaining how a stable batch of 5-aminoquinaldine pushed a complex synthesis through regulatory review in record time. We take both the praise and criticism straight back to our production team, adapting protocols where possible and providing honest answers where limits exist.

    From formulation troubleshooting to advice on upscaling, we don’t just ship material and disappear. Our in-house development lab trials new purification or drying methods every quarter, hunting for even minor yield improvements or process shortcuts. We believe this focus on continuous learning changes the benchmark for what customers expect. Through direct communication, user trust grows—each lot speaks not just to where it was made, but also to the people who stand behind it.

    Looking Toward the Future of Synthesis

    As the broader chemical industry shifts toward greener, leaner processes, 5-aminoquinaldine remains a workhorse in toolkits around the world. Our plant develops incremental refinements in synthesis and purification, targeting lower energy use and safer waste management. Many customers ask us about the future: Will new green-chemistry routes bring cost or performance breakthroughs? We share their curiosity and contribute what we learn through practical experimentation, not just theoretical projections.

    For those working in start-ups or facing tighter regulatory hurdles, consistent 5-aminoquinaldine supply can tip the scales. We don’t make empty promises about timelines or capacities; instead, we share what we know, highlight what we’re improving, and welcome partners to visit and see our production firsthand. This openness reflects over two decades of learning the value of transparency. Customers know what they’re getting, batch after batch, with no hidden surprises.

    Conclusion: Choosing the Right Quinoline for Results That Matter

    In the real world of chemical manufacturing and research, every decision counts. Why choose 5-aminoquinaldine over competitors? In our experience, the answer boils down to reliability—both in the molecule itself and the people who produce it. We take pride in delivering not just a pure compound but a service that includes responsive support, continuous process improvement, and an honest approach to customer needs. Whether you’re scaling up medicinal chemistry projects, developing new dyes, or pushing the boundaries in materials science, this product delivers the performance and consistency that seasoned professionals expect. We let our process and our people speak for themselves, bottle after bottle, shipment after shipment.