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4-Hydroxy-1-Methyl-2-Quinolone

    • Product Name 4-Hydroxy-1-Methyl-2-Quinolone
    • Alias N-Methylkynurenine
    • Einecs 211-969-7
    • 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

    402182

    Chemical Name 4-Hydroxy-1-Methyl-2-Quinolone
    Molecular Formula C10H9NO2
    Molecular Weight 175.19 g/mol
    Cas Number 1508-01-0
    Appearance Off-white to light yellow powder
    Melting Point 179-182 °C
    Solubility Slightly soluble in water; soluble in most organic solvents
    Purity Typically ≥98%
    Iupac Name 1-methyl-4-oxo-1,4-dihydroquinolin-2-one
    Smiles Cn1c(=O)c2ccccc2cc1O
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 1-Methyl-4-oxo-1,4-dihydroquinolin-2-one

    As an accredited 4-Hydroxy-1-Methyl-2-Quinolone 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 4-Hydroxy-1-Methyl-2-Quinolone; labeled with hazard symbols, product details, and safety instructions.
    Shipping 4-Hydroxy-1-Methyl-2-Quinolone is shipped in tightly sealed containers to prevent moisture and contamination. The packaging complies with chemical transport regulations, with labeling for identification and hazard communication. It is transported via ground or air, depending on destination, under conditions that prevent extreme temperatures and ensure safe delivery.
    Storage 4-Hydroxy-1-Methyl-2-Quinolone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Use chemical-resistant containers and store at room temperature, unless otherwise specified. Ensure appropriate labeling and follow all relevant safety regulations and guidelines for safe handling and storage.
    Application of 4-Hydroxy-1-Methyl-2-Quinolone

    Applications of 4-Hydroxy-1-Methyl-2-Quinolone in Industrial Manufacturing

    4-Hydroxy-1-Methyl-2-Quinolone serves as an advanced heterocyclic intermediate across multiple high-value industrial sectors, especially in the field of chemical synthesis and process manufacturing. Our direct production delivers consistent high purity, enabling reliable downstream integration for specialty and bulk manufacturers.

    1. Pharmaceutical Intermediate for Quinolone Antibiotics

    This compound functions as a key raw intermediate in the multistep synthesis of second-generation quinolone antibiotic APIs. Synthesis lines employ controlled reactions under GMP conditions to generate target structures through a defined pathway, ensuring batch reproducibility and precise impurity profiles required for regulated pharmaceutical markets. We provide material with defined traceability, allowing stringent quality assessment at every supply batch. Clients integrate this intermediate within stepwise condensation or cyclization processes in line with license requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Part II, Section 19 for intermediates
    • US FDA cGMP 21 CFR Part 210/211 for pharmaceutical use
    • EP/BP/USP pharmacopoeial impurity and residual solvent specifications adherence

    Typical usage ratio

    • Used at 0.6 to 1.2 molar equivalents relative to the core quinolone scaffold step; adjusted case by case to balance conversion vs. raw material cost efficiency.

    Downstream process integration

    • Added post-basification in the main synthetic reaction train as the source for methylation or functionalization.
    • Feeds directly into protected ring closure or further oxygenation transformations within GMP-validated reactors.
    • Lot control and reference standard cross-checks at each stage.

    Final product types

    • Ciprofloxacin and related fluoroquinolone antibiotic APIs
    • Generic finished pharmaceutical forms like tablets, solutions
    • Veterinary medicine quinolone actives

    2. Agrochemical Synthesis Building Block

    This compound features as a foundation for multi-step synthesis of heterocyclic pesticides and crop protection agents, especially in the functionalization or derivatization of quinolones for improved field stability and biological activity. Agrochemical customers use this input within registered synthesis methods validated for environmental safety, traceability, and batch reproducibility. Controlled formulations ensure minimal residuals—delivering compliant intermediate purity for registered active ingredient manufacture.

    Industry compliance standards

    • FAO/WHO specifications for technical grade pesticide intermediates
    • ISO 9001 for batch reproducibility
    • EU REACH (EC/1907/2006) registration for intermediate use
    • Chemical Manufacturers Association Responsible Care certifications

    Typical usage ratio

    • 10–35 wt% in main condensation or cyclization step, with ratio subject to target molecule and residues monitoring.

    Downstream process integration

    • Charged as the heterocyclic precursor after base or acid activation.
    • Integrated before halogenation or protective group chemistry according to regulated synthesis dossiers.
    • Monitored for conversion by HPLC or GC as part of full material balance.

    Final product types

    • Pyridone-derived fungicide active ingredients
    • Quinolone-based insecticidal intermediates
    • Herbicide advanced intermediates for pre-emergent control

    3. Specialty Dye and Pigment Manufacturing

    Heterocyclic rings from this product introduce tailored color and fastness characteristics in custom dye systems, particularly for technical textiles, coatings, and inkjets. Manufacturers select this compound to impart high UV and chemical resistance in industrial dye formulations where color stability and process repeatability are critical. We supply consistent material ready for advanced chromophoric transformations, supporting complex blending and downstream formulation quality demands in regulated sectors.

    Industry compliance standards

    • OEKO-TEX® Standard 100 certification for input chemical residue
    • ISO 9001 and ISO 14001 for responsible chemical processing
    • ZdhC MRSL v3.1 and REACH Annex XVII for commercial dye inputs
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines

    Typical usage ratio

    • 5–18 wt% in heterocyclic pigment intermediate, adjusted according to chroma and shade target in final formulation.

    Downstream process integration

    • Introduced during primary heterocycle coupling phase.
    • Subsequently functionalized or condensed into high-stability pigments under monitored temperature and pH conditions.
    • QC checks include HPLC color profile and heavy metal analyses before further blending.

    Final product types

    • Textile and polyester fiber dyes
    • High-performance industrial pigments
    • Digital inkjet dye precursors

    4. Laboratory Chemical & Research Synthesis

    This molecule represents a practical scaffold for academic and industrial R&D into new heterocycle chemistry, antimicrobial agents, and structure-activity relationship studies. Chemical supply for this application emphasizes lot transparency and small-batch purity. Research groups employ the material in custom syntheses, screening libraries, and medicinal chemistry route development, where regulatory documentation for non-clinical use and accurate COAs remain critical for publication and patent application.

    Industry compliance standards

    • ISO/IEC 17025 for analytical traceability
    • Internal laboratory chemical handling SOPs
    • GLP (OECD Principles of Good Laboratory Practice) for pre-clinical studies
    • Material Safety Data Sheet (MSDS) with full impurity disclosure

    Typical usage ratio

    • 0.1–1.5 mmol scale per reaction flask (adjusted based on screening library or multi-step yield requirements).

    Downstream process integration

    • Weighing and addition directly to the reaction vessel for exploratory synthesis.
    • Utilized in parallel synthesis workflows for high-throughput analysis.
    • Documentation and batch traceability for cross-study reproducibility.

    Final product types

    • Heterocycle analog libraries
    • Patentable chemical scaffolds
    • Preclinical lead candidates for pharmaceutical companies

    5. Electronic and Photonic Materials Precursor

    The compound supports development of advanced organic materials in the electronics industry, providing electron-rich aromatic rings for organic semiconductors, luminescent dyes, and sensor device prototypes. Downstream manufacturers select this raw material for its ability to introduce precise heteroatom positioning and electronic effects during film casting or device fabrication, with full control over polymerization or coupling reaction purity. Batch uniformity and analytical certificates from us enable reliable scale-up for pre-commercial device testing.

    Industry compliance standards

    • JEDEC JESD625 strict handling practices
    • ISO 9001 in advanced electronic materials production
    • REACH and RoHS compliance with full SVHC pre-check
    • TSE (Total Soluble Extractables) testing for low ionic/metal content

    Typical usage ratio

    • 1–10 mol% in precursor blends; tuned for desired electronic/optical performance in device layers.

    Downstream process integration

    • Solution-phase doping or precursor mixing for co-polymerization.
    • Compound deposited onto substrate prior to annealing or device encapsulation.
    • Final process includes purity validation via LC-MS or single crystal X-ray.

    Final product types

    • Organic TFT (thin-film transistor) materials
    • OLED emitter precursors
    • Chemical vapor deposition seeds for electronic sensors
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