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7-Nitro-1,2,3,4-Tetrahydroquinoline

    • Product Name 7-Nitro-1,2,3,4-Tetrahydroquinoline
    • Alias 7-Nitro-1,2,3,4-tetrahydroquinoline
    • Einecs 688-500-6
    • 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

    248561

    Chemical Name 7-Nitro-1,2,3,4-Tetrahydroquinoline
    Cas Number 93923-16-9
    Molecular Formula C9H10N2O2
    Molecular Weight 178.19
    Appearance Yellow to orange solid
    Melting Point 97-101 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1CCNC2=C1C=C(C=C2)[N+](=O)[O-]
    Inchi InChI=1S/C9H10N2O2/c12-11(13)8-3-1-2-7-6-10-5-4-9(7)8/h1-3,10H,4-6H2
    Storage Conditions Store in a cool, dry place, tightly sealed

    As an accredited 7-Nitro-1,2,3,4-Tetrahydroquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, clearly labeled “7-Nitro-1,2,3,4-Tetrahydroquinoline” and hazard warnings.
    Shipping 7-Nitro-1,2,3,4-Tetrahydroquinoline is shipped in sealed containers, protected from light, moisture, and extreme temperatures. It must comply with all applicable regulations for hazardous chemicals, including proper labeling and documentation. Ensure packaging prevents leaks or spills, and handle with care, using suitable personal protective equipment during transport and handling.
    Storage 7-Nitro-1,2,3,4-Tetrahydroquinoline should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers or acids. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical storage cabinets, and clearly label all containers. Always follow local regulations and laboratory safety protocols for storage.
    Application of 7-Nitro-1,2,3,4-Tetrahydroquinoline

    Applications of 7-Nitro-1,2,3,4-Tetrahydroquinoline in Industrial Manufacturing

    7-Nitro-1,2,3,4-Tetrahydroquinoline serves as a specialized intermediate in chemical synthesis, particularly impacting the pharmaceutical, agrochemical, pigment, specialty polymer, and fine chemical sectors. Manufactured under strict quality management systems, our material enables downstream producers to formulate targeted, compliant products in their respective fields.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical manufacturing, downstream formulators use this compound as a key building block for synthesizing various active ingredients, especially within central nervous system (CNS) therapies and anti-infective drugs. It supports the construction of nitrogen-containing heterocycles crucial to drug molecules. Pharmacological research protocols often require this intermediate to maintain high consistency in purity and particle size, as these factors can influence final bioavailability and batch reproducibility.

    Industry compliance standards

    • Good Manufacturing Practice (ICH Q7, EU GMP, US cGMP)
    • Ph. Eur., USP/JP, and ChP monograph compliance (where applicable for end API)
    • REACH (EU) and TSCA inventory registration (US)
    • Controlled substance precursor monitoring under national laws

    Typical usage ratio

    • Ranging from 0.25 to 2.2 molar equivalents depending on target API route
    • Adjustments based on desired yield, purity profile, and process scale

    Downstream process integration

    • Enters initial heterocyclization or nitration stages in multi-step batch synthesis
    • Employed in condensation or reduction reactions for core scaffold construction
    • Packaged under nitrogen for direct transfer to GMP reactor suites

    Final product types

    • CNS-targeted medicinal APIs (e.g., dopaminergic agents, modulators)
    • Broad-spectrum antimicrobial agents
    • Experimental compounds for Phase I–III clinical development

    2. Agrochemical Intermediate for Herbicide Synthesis

    Major agrochemical producers utilize this compound as a fixed-ring intermediate to construct selective herbicide actives, targeting grass and broadleaf weeds. Its electron-deficient aromatic system is well-suited for enzymatic inhibition chemistry, contributing to sustainable agricultural practices. Quality comes controlled to minimize residual solvents and byproducts, supporting adherence to residue limits in finished formulations.

    Industry compliance standards

    • FAO/WHO technical material specifications (ISO 1750 series)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • EPA guidelines for pesticide intermediates (40 CFR Part 158)
    • Integrated Pest Management (IPM) output compliance

    Typical usage ratio

    • 3–10% by weight in the synthesis stage, relative to total batch mass
    • Dosage refined per targeted molecule structure and reaction yield

    Downstream process integration

    • Stage-wise incorporation during catalytic coupling or amination steps
    • Introduced into closed-loop reactors to prevent environmental release
    • Followed by in-process QC for nitro group conversion efficiency

    Final product types

    • Post-emergent selective herbicides
    • Pre-mix tank formulation bases
    • Active ingredients for integrated crop protection products

    3. Intermediate in Specialty Pigment Manufacture

    In technical pigment production, chemical companies use this molecule to synthesize high-stability yellow, orange, or red pigments based on quinoline chromophores. The controlled nitro substitution on the tetrahydroquinoline ring enhances lightfastness and chemical resistance, critical for coatings, plastics, and textile dyes demanding high performance under exposure.

    Industry compliance standards

    • ISO 9001:2015 for pigment production
    • EN 71-3 (Safety of toys—Migration of certain elements, applicable for pigment safety)
    • EU RoHS 2011/65/EU for electronics-related colorants
    • ETAD/REACH registration for pigment precursors

    Typical usage ratio

    • 5–25% by weight in initial pigment precursor batch
    • Ratio varies by shade, process (azo coupling vs. condensation), and substrate

    Downstream process integration

    • Mixes with diazotized partners in chromophore-building stages
    • Processed in aqueous/solvent media to ensure homogeneity
    • Incorporated before filtration and milling to pigment grade specification

    Final product types

    • Organic pigment dispersions for plastics and paints
    • High-fidelity textile dyes
    • Color concentrates for polymeric masterbatches

    4. Precursor for Specialty Polymer Synthesis

    R&D and manufacturing teams in the specialty polymer field use this compound for synthesizing high-performance resins and coatings. The nitro group facilitates post-polymerization modification, enabling precise control of polymer architecture and side-chain functionalities for electronic, optical, or barrier applications. Processing requires careful temperature and pH control to preserve integrity and avoid structural decomposition.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • UL 94 (for polymer flammability rating, downstream)
    • REACH and US EPA premanufacture notification (PMN) for new polymers
    • GHS/CLP classification for intermediates

    Typical usage ratio

    • 0.5–8% by weight relative to total monomer input per batch
    • Fine-tuned to achieve required molecular weight and crosslinking density

    Downstream process integration

    • Charged during primary monomer blending before chain initiation
    • Participates in step-growth or free-radical polymerization stages
    • Isolated from final resin by vacuum distillation if necessary

    Final product types

    • UV-cured coatings for electronic substrates
    • Barrier resins for chemical-resistant packaging
    • Conductive polymers for antistatic and ESD applications

    5. Intermediate for Fine Chemical Synthesis in OLED Materials

    Developers of organic electronic materials employ this compound in building block synthesis for organic light-emitting diodes (OLED) and other optoelectronic devices. Its structural profile supports functionalization toward hole-transport or emission layer materials. Controlled impurity levels below 0.1% ensure high device efficiency and long operational lifespan, as electronic applications require minimal residual ionic contaminants.

    Industry compliance standards

    • IPC-1752A (Material Declaration Management for Electronics)
    • RoHS 2.0/3.0 for display material safety
    • ISO 14644-1 Cleanroom Standards for optoelectronic manufacturing
    • REACH registration for fine chemicals

    Typical usage ratio

    • 0.1–2% by weight in precursor blend (dependent on device layer composition)
    • Adjusted for specific light emission efficiency and stability targets

    Downstream process integration

    • Integrated during late-stage organometallic or arylation reactions
    • Fed into multi-step purification and vacuum sublimation lines
    • Packaged under inert gas for direct transfer to clean manufacturing environments

    Final product types

    • Emission layer materials for OLED displays and lighting panels
    • Hole/injection transport layers in organic semiconductors
    • Advanced fine chemicals for electronic inks and sensors

    6. Synthesis of Chemical Reference Standards

    Analytical laboratories and QC units source this material to prepare reference standards, enabling precise calibration and validation of analytical methods, including HPLC, LC-MS, and GC for presence in regulated products. Each batch undergoes stringent impurity and trace metal testing, with detailed certificates of analysis provided for regulatory submissions.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • IUPAC standards for analytical reference materials
    • European Pharmacopoeia/USP guidelines on reference standards
    • 21 CFR Part 211 – CGMP for finished pharmaceuticals (applicable in analytics)

    Typical usage ratio

    • Prepared at concentrations ranging from 1–1000 mg/L for analytical solutions
    • Exact concentration determined by targeted method sensitivity and range

    Downstream process integration

    • Aliquoted in traceable vials under inert atmosphere
    • Used immediately or stored in desiccated, light-proof conditions
    • Directly compared with test and sample lots for method validation

    Final product types

    • Primary and secondary reference standards for analytical QC
    • System suitability test mixtures
    • Calibration curves for regulated industry testing
    Free Quote

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