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4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline

    • Product Name 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline
    • Alias 4-Chloro-2-methyl-7-(trifluoromethyl)quinoline
    • Einecs 630-882-5
    • 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

    595425

    Productname 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline
    Molecularformula C11H6ClF3N
    Molecularweight 247.62 g/mol
    Casnumber 1015132-69-4
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Slightly soluble in common organic solvents
    Smiles CC1=NC2=CC(=C(C=C2C=C1Cl)C(F)(F)F)
    Inchi InChI=1S/C11H6ClF3N/c1-6-15-9-4-3-7(11(13,14)15)5-8(9)10(12)2-6/h2-5H,1H3
    Storageconditions Store at room temperature, away from moisture and light
    Synonyms 7-(Trifluoromethyl)-4-chloro-2-methylquinoline

    As an accredited 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a tamper-evident cap, labeled with chemical name, CAS number, and hazard symbols.
    Shipping 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled by trained personnel, in compliance with local and international regulations for hazardous chemicals. Ensure proper labeling, documentation, and transport under conditions that prevent spills or accidental exposure.
    Storage Store **4-Chloro-2-Methyl-7-(Trifluoromethyl)quinoline** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizers. Ensure containers are clearly labeled. Access should be restricted to trained personnel, and proper personal protective equipment (PPE) should be used when handling the chemical.
    Application of 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline

    Applications of 4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline in Industrial Manufacturing

    4-Chloro-2-Methyl-7-(Trifluoromethyl)Quinoline serves as a critical intermediate in several advanced chemical sectors. Our facility controls the complete process chain, enabling accurate conformity with evolving industry standards and supporting consistent integration into demanding downstream applications. We address the precise needs of the pharmaceutical, agrochemical, pigment, and electronic material sectors.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Antimalarial Drug Intermediates

    Pharmaceutical manufacturers utilize this compound primarily as a key intermediate in the synthesis of quinoline-based antimalarial APIs. We ensure consistent chemical purity to meet current pharmacopeia specifications. Our technical support assists with process validation for regulated environments, focusing on precise charging during the condensation and cyclization steps. Downstream partners integrate this molecule during the heterocyclic ring formation stage to achieve the structure-activity requirements of the final API, which often forms part of combination antimalarial therapies distributed under strict approval protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Regulation (EC) No 1907/2006 (REACH) for chemical safety
    • United States Pharmacopeia (USP) monographs for related APIs
    • EDQM CEP and WHO Prequalification for antimalarial drug supply

    Typical usage ratio

    • 0.2–1.0 molar equivalents per batch, adjusted according to optimized synthetic yield and impurity control strategy

    Downstream process integration

    • Charged at quinoline ring formation step following directed chlorination/coupling reactions
    • Included in in-process QC prior to final API crystallization and purification

    Final product types

    • Active antimalarial pharmaceutical compounds (e.g., piperaquine, chloroquine analogues)
    • Combination antimalarial treatments

    2. Agrochemical Intermediate for Herbicide Synthesis

    Leading agrochemical formulators use our material as a core intermediate in quinoline-derived herbicidal agent production. The compound's electron-withdrawing substituents play a pivotal role in achieving target selectivity against specific weed genotypes in broadacre crops. Typical integration occurs at the heterocycle assembly stage, where process engineers monitor conversion and byproduct content according to both local and global safety frameworks. Final herbicides pass through dedicated downstream reactors and purification columns before micronization and blending for direct-to-field formulations.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) standards
    • OECD Principles of Good Laboratory Practice (GLP)
    • China National Food Safety Standard for maximum residue limits (GB 2763)
    • EU Regulation (EC) No 1107/2009 for active plant protection substances

    Typical usage ratio

    • 5–15% by weight in the active intermediate synthesis step, determined by target yield and downstream lead compounds

    Downstream process integration

    • Supplied at core heterocyclic coupling stage in the main reaction vessel
    • Subject to continuous residual solvent analysis before isolation

    Final product types

    • Selective pre-emergent and post-emergent herbicides
    • Formulated crop protection granules and suspensions

    3. High-Performance Pigment and Dye Manufacturing

    Manufacturers of specialty pigments for applications such as industrial inks, plastics, and coatings use our compound as a building block in quinoline-based pigment synthesis. The starting material enters diazotization and subsequent coupling reactions in pigment plants, imparting excellent light and heat stability to the final dispersions. Precise dosing responds to desired color intensity and fastness parameters, especially for high-temperature polymer processing and UV-resistant printing applications. Integrated process sampling and spectral analysis ensure consistency in chromophore development.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for pigment production
    • EN 71-3 migration limits for heavy metals in toys and inks
    • REACH Annex XVII restrictions for hazardous pigment components
    • ASTM D5538 for color and gloss standards in industrial coatings

    Typical usage ratio

    • 8–25% by mass in pigment precursor charge, depending on polymer compatibility and desired chromatic properties

    Downstream process integration

    • Introduced during diazo coupling and condensation stages
    • Subject to on-line absorbance testing during dispersion

    Final product types

    • High-stability organic pigments
    • Industrial-grade colorants for plastics and engineered polymers
    • Inks for specialty printing and high-performance coatings

    4. Electronic Material Precursors – OLED and Liquid Crystal Applications

    Global electronics manufacturers adopt our quinoline derivative as a specialty intermediate for synthesizing advanced organic compounds deployed in OLED displays and liquid crystal devices. The molecule’s fluorinated and methylated functionality adjusts charge transport and emission wavelength in photoactive layers. Material handling requires precise moisture and particulate control prior to introduction within condensation and cyclization modules. Downstream, product integration strictly adheres to semiconductor-grade quality testing and traceability requirements.

    Industry compliance standards

    • IPC-4101/126 for electronic material base requirements
    • JEITA ET-7403 standards for organic semiconductors
    • IEC 61249-2-41 for base material halogen content limits
    • RoHS Directive 2011/65/EU for hazardous substance restrictions

    Typical usage ratio

    • 1–6% by weight within the active organic conjugated layer precursor solution, optimized according to device architecture and emission spectra targets

    Downstream process integration

    • Weighing and dispensing under cleanroom conditions for batch-wise solution preparation
    • Incorporation into vacuum deposition or wet processing unit operations

    Final product types

    • OLED (organic light-emitting diode) display pixels
    • Advanced liquid crystal display (LCD) alignment materials
    • Photoresponsive layers in consumer and industrial electronics

    5. Custom Fine Chemical Synthesis for Research Use

    Chemical research institutions and custom synthesis laboratories source this intermediate for structure-activity relationship (SAR) studies and the discovery of novel quinoline-based functional materials. Our manufacturing documentation supports traceable lot tracking and analytical verification for regulated environments. End users adjust introduction volumes based on specific synthetic pathways, often incorporating the material at the nucleophilic aromatic substitution or Friedländer quinoline construction steps. All batches are accompanied by validated certificate of analysis reports to support reproducibility in exploratory synthesis.

    Industry compliance standards

    • ISO 17034 Reference Material Producer accreditation (for supplied standards)
    • GLP requirements for analytical reference standards
    • Relevant GHS labeling for research chemicals
    • Material Safety Data Sheet (MSDS) compliance for laboratory handling

    Typical usage ratio

    • Variable 0.05–0.5 equivalents in standard research-scale reactions; calculated to allow route diversification or impurity profiling as required

    Downstream process integration

    • Dosed during initial exploratory synthetic sequence or SAR investigation
    • Documented via batch-specific COA and NMR/LCMS analyses

    Final product types

    • SAR libraries for drug discovery
    • Reference standards for academic and pharmaceutical R&D
    • Custom intermediates for contract chemical synthesis
    Free Quote

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