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2-Methoxy-4-Nitrophenyl Isothiocyanate

    • Product Name 2-Methoxy-4-Nitrophenyl Isothiocyanate
    • Alias MNIT
    • Einecs (EINECS) 400-860-4
    • 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

    950325

    Chemical Name 2-Methoxy-4-Nitrophenyl Isothiocyanate
    Cas Number 61060-81-1
    Molecular Formula C8H6N2O4S
    Molecular Weight 226.21 g/mol
    Appearance Yellow crystalline powder
    Melting Point 97-99 °C
    Boiling Point No data available
    Solubility Slightly soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Smiles COC1=CC(=C(C=C1)N=C=S)[N+](=O)[O-]
    Inchi InChI=1S/C8H6N2O4S/c1-14-8-4-6(9-5-15)2-3-7(8)10(11)12/h2-4H,1H3

    As an accredited 2-Methoxy-4-Nitrophenyl Isothiocyanate 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 5 grams of 2-Methoxy-4-Nitrophenyl Isothiocyanate, tightly sealed, labeled with hazard warnings and specifications.
    Shipping 2-Methoxy-4-Nitrophenyl Isothiocyanate is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is classified as hazardous and should be handled according to all relevant safety and transport regulations. Shipping includes appropriate labeling and documentation to ensure safe delivery and compliance with international chemical transport standards.
    Storage 2-Methoxy-4-nitrophenyl isothiocyanate should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight and moisture. Keep it separate from incompatible substances such as strong acids, bases, and oxidizing agents. Store at room temperature, avoiding extreme temperatures. Properly label the container and use appropriate chemical safety protocols when handling and storing.
    Application of 2-Methoxy-4-Nitrophenyl Isothiocyanate

    Applications of 2-Methoxy-4-Nitrophenyl Isothiocyanate in Industrial Manufacturing

    As a direct manufacturer of 2-Methoxy-4-Nitrophenyl Isothiocyanate, we support various specialty chemical industries by supplying this intermediate for focused, regulated downstream sectors. Below we detail the primary industrial fields where our raw material enables specific formulation and synthesis processes, with attention to compliance, reasonable usage ratios, integration points, and actual finished goods.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use 2-Methoxy-4-Nitrophenyl Isothiocyanate to build thio-containing intermediates required in targeted active pharmaceutical ingredients (APIs). This compound reacts selectively with amines to form stable thiourea analogs under controlled conditions. Developers adjust input concentration based on the desired stoichiometry of the specific synthesis route, ranging from selective inhibitors to anticancer molecule precursors. Strict traceability, impurity control, and GMP validation guide every batch for end-to-end pharmaceutical compliance.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • EU Guidelines for APIs (EMA)
    • US FDA 21 CFR Part 210/211
    • Ph. Eur. and USP monograph references

    Typical usage ratio

    • 0.90 – 1.20 molar equivalents vs. target amine reactant; adjusted based on final intermediate purity and yield optimization studies

    Downstream process integration

    • Charged into API synthesis reaction tank following solvent and base charge; addition rate and temperature regulated to control exotherm and completion based on in-process QC

    Final product types

    • Antineoplastic intermediates
    • Kinase inhibitor scaffolds
    • Anti-inflammatory API cores
    • Custom synthetic building blocks for contract pharma

    2. Agrochemical Intermediate Manufacturing

    Agrochemical formulators incorporate this isothiocyanate as a key step in constructing sulfur-containing heterocycles relevant to certain amide and carbamate herbicides or fungicides. Its high specificity yields high-purity intermediates, meeting robust environmental and residual control requirements. Manufacturing teams validate input percentages based on targeted intermediate batch sizes, all while maintaining compliance with local chemical regulations and mandatory quality audits for agrochemical synthesis.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH Regulation (EC No 1907/2006)
    • China National Agrochemical Standards (GB/T)

    Typical usage ratio

    • 1.05 – 1.15 equivalents relative to nucleophilic coupling partners depending on final product residue limit targets

    Downstream process integration

    • Dosed into enclosed reactors post-solubilization of the primary aromatic substrate; addition follows temperature ramp and agitation cycle designed to minimize by-product formation and maximize yield

    Final product types

    • Carbamate herbicide intermediates
    • Thiocarbamate fungicide building blocks
    • Sulfur-heterocycle agro-input additives

    3. Dye and Pigment Synthesis for Electronics

    Electronic materials producers use 2-Methoxy-4-Nitrophenyl Isothiocyanate to synthesize functionalized aromatic dyes and pigment intermediates necessary for high-resolution display manufacturing. Its stable isothiocyanate functionality reacts under anhydrous conditions with specialized amines, facilitating controlled dye formation for advanced color filter arrays. To achieve precise shade, intensity, and purity, process teams calibrate raw material charge rates per colorant batch, subject to strict electronics Industry QC and process validation requirements.

    Industry compliance standards

    • RoHS Directive 2011/65/EU
    • IEC 61249-2-21 Halogen-free Standard (for electronics)
    • ISO 9001:2015 (quality systems in colorant industry)

    Typical usage ratio

    • 0.8 – 1.1 molar equivalents versus amine-based dye-forming agents, modulated by target color profile and application process scale

    Downstream process integration

    • Added during condensation step after base color backbone preparation; feed rate monitored to reduce side reactions and achieve uniform pigment particle size

    Final product types

    • Organic electrophotographic pigments (OEPs)
    • Liquid crystal display (LCD) dye precursors
    • High-purity color filter materials for OLED and TFT modules

    4. Specialty Polymer Modifier Production

    Advanced polymer engineers utilize this isothiocyanate for post-polymerization modification of specialty resins, introducing reactive thiourea or isothiourea groups to tailor polymer surface activity or crosslink density. The addition occurs under controlled heat and catalyst conditions, supporting development of adhesives, coatings, and specialty membranes demanded in filtration and separation technologies. Stringent handling and residue specifications apply, as do strict batch-level quality records.

    Industry compliance standards

    • ISO 14001:2015 (environmental management in chemical processing)
    • REACH Regulation for new material notification
    • China Compulsory Certification (CCC) for specialty polymer end-uses

    Typical usage ratio

    • 0.5 – 2.0 weight % to total polymer feed, adjusted per compatibility and degree of modification required in end-use resin

    Downstream process integration

    • Injected or drip-fed post-polymerization, prior to extrusion or mold-filling step, ensuring uniform distribution and surface functionality control

    Final product types

    • Functionalized film-forming resins
    • Adhesive and coating polymers
    • Membrane materials for selective separation

    5. Analytical Reagent Manufacturing for Life Sciences

    Life science reagent producers employ this isothiocyanate for synthesis of derivatization agents utilized in proteomics, peptide mapping, and amino acid analysis. It serves as a reactant to prepare chromogenic or fluorogenic reagents, enhancing sensitivity and detection in high-performance liquid chromatography (HPLC) and related methods. Preparation protocols demand highly controlled ratios and purity, with compliance to reagent grade specification and batch homogeneity.

    Industry compliance standards

    • ISO 13485 Medical Device Quality System
    • Certificate of Analysis (CoA) for Reagent & ACS grades
    • US Pharmacopeia (USP) for analytical reagents

    Typical usage ratio

    • 1.0 – 1.3 equivalents per analyte or derivatizing base, tailored to the specific analytical workflow and target analytical sensitivity

    Downstream process integration

    • Blended under anhydrous or inert conditions in preparation vessels, followed by packaging as preweighed derivatization kits or ready-to-use reagents for laboratory workflows

    Final product types

    • HPLC labeling reagents for amino acid analysis
    • Chemiluminescent or fluorescent probe kits
    • Chromogenic standards for protein and peptide mapping
    Free Quote

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