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2-Nitrophenyl Selenocyanate

    • Product Name 2-Nitrophenyl Selenocyanate
    • Alias 2-NO2-Ph-SeCN
    • Einecs 238-876-4
    • 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

    786973

    Chemical Name 2-Nitrophenyl Selenocyanate
    Cas Number 27140-12-3
    Molecular Formula C7H4N2O2Se
    Molar Mass 241.09 g/mol
    Appearance Yellow to orange solid
    Melting Point 94-98°C
    Solubility Slightly soluble in common organic solvents
    Purity Typically ≥98%
    Storage Temperature Store below 30°C, protected from light and moisture
    Synonyms o-Nitrophenyl selenocyanate
    Smiles C1=CC=C(C(=C1)[N+](=O)[O-])[Se]C#N
    Inchi InChI=1S/C7H4N2O2Se/c8-5-13-6-3-1-2-4-7(6)9(10)11/h1-4H

    As an accredited 2-Nitrophenyl Selenocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed cap, hazard labels, product name and CAS displayed, contains 5 grams of 2-nitrophenyl selenocyanate.
    Shipping 2-Nitrophenyl Selenocyanate is shipped in tightly sealed containers, protected from light and moisture. Transport requires compliant hazardous materials packaging and labeling. The substance should be stored at room temperature, away from incompatible materials. Shipping follows relevant international and local regulations for handling toxic and potentially harmful chemicals.
    Storage 2-Nitrophenyl Selenocyanate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight. Keep it away from sources of ignition, moisture, and incompatible materials like strong oxidizers. Proper labeling and secondary containment are advised to prevent accidental exposure. Handle under a fume hood and use appropriate personal protective equipment.
    Application of 2-Nitrophenyl Selenocyanate

    Applications of 2-Nitrophenyl Selenocyanate in Industrial Manufacturing

    2-Nitrophenyl Selenocyanate serves as a specialized reagent and intermediate in several advanced chemical manufacturing processes. Our direct supply supports high-purity needs for pharmaceutical, agrochemical, and specialized materials producers. Below, we outline representative downstream applications in real industrial sectors, focusing on application-specific compliance, technical formulation, and end-use integration.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use this compound in constructing organoselenium-containing APIs, especially in the synthesis of novel anti-tumor, anti-inflammatory, and anti-infective agents. Its role as a selenium donor facilitates the preparation of selenoethers, selenoamides, and functionalized small molecules. Process engineers select batch or continuous synthesis routes depending on the target molecule and scale, applying strict in-process controls to ensure purity and minimize residual selenium. Handling protocols and dosing are adapted to comply with cGMP and pharmacopoeial monographs for each finished drug.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for APIs
    • USP and Ph. Eur. monographs (where applicable for selenium APIs)
    • FDA 21 CFR Part 211
    • EMEA/CHMP Quality Guidelines

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to core substrate, adjusted based on required selenium incorporation and byproduct minimization.

    Downstream process integration

    • Added in the selenation stage following aromatic substitution steps.
    • Applied under inert atmosphere (e.g., argon or nitrogen), temperature controlled (10–30°C).
    • Residuals removed by aqueous or solvent extractions, followed by silica gel chromatography or preparative HPLC.

    Final product types

    • Anticancer agents incorporating organoselenium motifs
    • Selenium-based enzyme inhibitors
    • Precursor molecules for CNS-active drug candidates
    • Selenoprotein mimetics for rare disease research

    2. Agrochemical Intermediate Manufacturing

    Producers of crop-protection chemicals employ this reagent for the selenocyanation of aromatic and heterocyclic cores in the research and development of selective fungicides and insecticides. The compound's reactivity under controlled conditions supports targeted modification of precursor molecules, allowing for tunable performance characteristics and environmental behavior. In all applications, manufacturers comply with international pesticide ingredient guidelines and restrict batch impurity profiles according to downstream registration requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients
    • OECD Guidance for Industry Data Submissions
    • REACH (Regulation (EC) No 1907/2006) for intermediates
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing

    Typical usage ratio

    • 1–3 molar equivalents per aromatic precursor; ratio refined based on stability of selenocyanate group and downstream formulation goals.

    Downstream process integration

    • Reacted post-halogenation or nitration stage of active ingredient synthesis.
    • Integrated immediately before protection or cyclization steps, often in batch reactors with automated feed control.
    • Byproduct selenium streams monitored for safe disposal to prevent environmental release.

    Final product types

    • Triazole-based fungicides with selenium-modified activity spectrum
    • Selenylated insecticide intermediates
    • Specialty crop-protection molecules for research pipelines

    3. Custom Organic Material Production

    Specialty material manufacturers incorporate this chemical as a selective selenium donating agent to modify organic electronic and optical materials. Precisely controlled addition enables the creation of conjugated polymers and low-molecular-weight compounds exhibiting enhanced conductivity, photostability, or charge transport. Process developers employ this step to structure-morphology relationships relevant for advanced device prototyping, adhering to strict in-house and market standards.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems
    • RoHS Directive (for materials entering electronics supply chain)
    • EN 62321 determination of certain hazardous substances
    • Customer-specific NDA and proprietary materials protocols

    Typical usage ratio

    • 0.2–1.2 equivalents per target functional group, depending on required selenium loading and end-use application; process optimization via small-scale scouting.

    Downstream process integration

    • Utilized during the functionalization of monomer or polymer backbones at late synthetic stages.
    • Employed under strictly controlled temperature and atmosphere to prevent over-oxidation of selenium moieties.
    • Incorporation often followed by solvent removal, film casting, or extrusion for further device assembly.

    Final product types

    • Selenylated polyaromatic films for flexible electronics
    • Organic photovoltaic module coatings
    • Charge transport additives for OLED manufacturing
    • Prototyping materials for chemical sensing devices

    4. Analytical Reagent Formulation

    Laboratory and specialty reagent producers formulate analytical kits using this compound for selenium determination, aryl-selenocyanate derivatization strategies, and mechanistic studies in academic and industrial research. Its selective reactivity allows researchers to derivatize specific functional groups, facilitating high-sensitivity quantitation and mechanistic tracking by chromatographic or spectroscopic methods. Quality-control teams rigorously test each batch to ensure low residual impurities and conformity to research-grade specifications.

    Industry compliance standards

    • ISO 17025 General requirements for the competence of testing and calibration laboratories
    • OECD Good Laboratory Practice (GLP)
    • ASTM E2882 guideline for selenium analysis reagents
    • Relevant national metrology standards for reference material suppliers

    Typical usage ratio

    • 5–50 µmol per reaction setup in laboratory-scale analysis; scalable for bulk reagent packs according to customer method development.

    Downstream process integration

    • Packaged as a ready-to-use component in analytical kits.
    • Integrated into QC protocols for pharmaceutical and material production facilities.
    • Shipped with COAs documenting purity, stability, and certified assay values.

    Final product types

    • Custom research reagents for HPLC, GC-MS, and spectrophotometric assays
    • Analytical kit components for environmental selenium monitoring
    • Calibrants and standards for material analysis laboratories
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