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2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole

    • Product Name 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole
    • Alias Tetrahydro-β-carboline
    • Einecs 216-503-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    545258

    Cas Number 1576-35-8
    Molecular Formula C11H12N2
    Molecular Weight 172.23 g/mol
    Iupac Name 2,3,4,5-Tetrahydro-1H-pyrido[4,3-b]indole
    Synonyms Tetrahydro-β-carboline
    Appearance Off-white to light yellow solid
    Melting Point 98-100°C
    Boiling Point 345.2°C at 760 mmHg
    Solubility In Water Slightly soluble
    Smiles C1CNCC2=C1C3=CC=CC=C3N2

    As an accredited 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical `2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole` is packaged in a 10-gram amber glass bottle with tamper-evident seal.
    Shipping **Shipping Description:** 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-b]indole should be shipped in tightly sealed containers, away from light, heat, and moisture. It is recommended to package the chemical securely to prevent spillage or contamination. Comply with all relevant regulations for handling organic chemicals, including appropriate labeling and documentation during transit.
    Storage 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-b]indole should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect from light, moisture, and incompatible substances such as strong oxidizers. Use appropriate safety precautions, including gloves and goggles, when handling, and label the storage container clearly to avoid accidental misuse or contamination.
    Application of 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole

    Applications of 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole in Industrial Manufacturing

    As a chemical raw material manufacturer, we provide high-purity 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole for specialized industrial sectors. Our production supports strict quality control, enabling reliable integration into advanced processes across several chemical and pharmaceutical downstream fields.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediates

    Originating from our controlled synthesis facility, this compound serves as an essential intermediate in the synthesis of indole-derived APIs, particularly in central nervous system (CNS) agent development. Medicinal chemistry teams utilize its unique tetrahydroindole backbone for stepwise transformations in alkaloid and heterocyclic drug synthesis pipelines, balancing purity requirements with process yields for target drug candidates. QC and regulatory compliance apply at all intermediates export stages to ensure suitability for further conversion in regulated API manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API Intermediate Supply
    • USP–NF Reference Standards (for final APIs only, not intermediates)
    • Client-specific QC and documentation as required by downstream Drug Master Files (DMFs)

    Typical usage ratio

    • Used in equimolar or slight excess (1:1 to 1.2:1 molar ratio) relative to core coupling or cyclization steps
    • Adjustment based on impurity profile and overall synthetic route efficiency

    Downstream process integration

    • Feedstock for nitrogen-based ring closure and substitution reactions in API synthesis lines
    • Typically introduced post-initial amination/condensation reactions, upstream of final salt formation
    • Supports both batch and flow chemistry setups in kilo-lab and industrial scales

    Final product types

    • CNS-active pharmaceutical substances (e.g., potential antipsychotics and antidepressants, subject to further development)
    • Licensed intermediates for clinical pipeline R&D molecules
    • Small-molecule drugs based on indole and pyridoindole frameworks

    2. Agrochemical Research Intermediates

    Our material features as a key building block in synthetic routes for research-grade development of plant protection product candidates, including probe compounds and analytical reference standards. Industrial clients engage it during lead optimization phases, where its structural motifs serve for bioisosteric replacement and derivatization before moving into pilot production of promising agrochemical agents.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • OECD Principles of Good Laboratory Practice (GLP) for research intermediates
    • REACH Regulation (EC) No 1907/2006—Registration for R&D Use
    • Recordkeeping required for Category 2 chemical intermediates under EU/US pesticide development regulation

    Typical usage ratio

    • 10–40% by moles in early-stage syntheses, tailored to combinatorial library design or new active moiety construction
    • Scaling adjusted for SAR cycle throughput and downstream purification requirements

    Downstream process integration

    • Utilized after initial coupling steps to introduce nitrogen heterocycles into candidate molecules
    • Integrated into small batch or parallel synthesis protocols for library creation
    • Purified by chromatographic or crystallization methods prior to bioactivity screening

    Final product types

    • Reference standards for structure-activity relationship (SAR) programs
    • Novel herbicidal and fungicidal lead compounds for further optimization
    • Chemical probes for mode-of-action studies in crop protection R&D

    3. Organic Electronic Material Synthesis

    Leading electronic material innovators employ this compound as a heteroaromatic core for fabrication of organic semiconducting layers. It functions as a foundational scaffold in precursor routes for specialty dyes, small-molecule conductors, and charge transport intermediates. Rigid electronic device QC and materials purity benchmarks apply throughout downstream film and device manufacturing.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) for electronic materials
    • IEC 61249-2-21 standards for halogen-free electronic components
    • Internal customer-driven purity and trace metal contents specifications
    • ISO 9001:2015 Quality Management Systems for electronic chemical processing

    Typical usage ratio

    • 2–10% by weight in batch syntheses for small-molecule organic electronic precursors
    • Modified for fitting into device-specific performance parameters (charge mobility, color)

    Downstream process integration

    • Enters after halogenation, alkylation, or acylation steps in precursor design
    • Deployed upstream of spin-coating or vapor deposition in thin-film device assembly
    • Requires advanced purification (≥99.5% GC/HPLC purity) to meet electronic-grade specs

    Final product types

    • Small-molecule organic light-emitting diodes (OLEDs) precursors
    • Photoactive dyes for organic photovoltaic cells
    • Charge transport materials in flexible printed electronic circuits

    4. Specialty Dye and Pigment Synthesis

    Producers of specialty dyes integrate this material as a nitrogen-rich heterocyclic component, targeting high-performance pigment synthesis for printing and technical textile applications. Downstream users value its reactivity profile in multi-step coloring agent development, focusing on lightfastness and solvent-fastness during finished goods formulation.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile applications (finished dyes and pigments only)
    • REACH Annex XVII compliance for azo compounds and aromatic amine precursors
    • ISO 105 Series for colorfastness testing in formulated pigment dispersions
    • Customer-specific emission and leaching assessment protocols

    Typical usage ratio

    • 20–55% molar ratio in core pigment backbone formation
    • Adjusted for target shade, application method, and process waste control

    Downstream process integration

    • Incorporated after diazotization or coupling reactions in pigment precursor manufacturing
    • Forms the technical base for colorant molecule extension and complexation
    • Subject to final purification steps prior to formulation into dispersions or pastes

    Final product types

    • Special effect pigments for inkjet and screen printing
    • Technical dyes for polyester and polyamide fiber coloration
    • Stable pigment granules for high-specification industrial coatings
    Free Quote

    Competitive 2,3,4,5-Tetrahydro-1H-Pyrido[4,3-B]Indole prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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