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Ethyl Isothiocyanate

    • Product Name Ethyl Isothiocyanate
    • Alias Mustard oil
    • Einecs 211-234-5
    • 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

    616381

    Product Name Ethyl Isothiocyanate
    Chemical Formula C3H5NS
    Molar Mass 87.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 132-134 °C
    Melting Point -88 °C
    Density 0.980 g/cm³ at 20 °C
    Solubility In Water Insoluble
    Refractive Index 1.507
    Flash Point 30 °C
    Odor Pungent, mustard-like
    Cas Number 542-85-8

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

    Packing & Storage
    Packing Ethyl Isothiocyanate is packaged in a 100 mL amber glass bottle with a secure cap and hazard warning label.
    Shipping Ethyl Isothiocyanate should be shipped in tightly sealed containers, clearly labeled, and compliant with hazardous materials regulations. It must be kept away from heat, open flames, and incompatible substances. Utilize appropriate secondary containment and cushioning. Transport via approved carriers for chemicals, ensuring all documentation and safety data sheets (SDS) accompany the shipment.
    Storage Ethyl isothiocyanate should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, sources of ignition, and incompatible materials such as strong oxidizing agents. The storage area should be equipped with suitable ventilation and spill containment. Always label containers clearly and keep them away from heat, moisture, and incompatible substances to prevent hazardous reactions.
    Application of Ethyl Isothiocyanate

    Applications of Ethyl Isothiocyanate in Industrial Manufacturing

    Ethyl isothiocyanate serves as a specialized building block in high-value industrial synthesis, especially where isothiocyanate groups are essential to targeted downstream reactions. Our material directly supports customers in agrochemical intermediates, specialty pharmaceutical manufacturing, rubber auxiliary synthesis, advanced organic synthesis, and select plastics modifier formulations. Below we describe established industrial application scenarios, with focus on compliance, technical usage, process stages, and concrete end products.

    1. Agrochemical Intermediate Synthesis

    Agrochemical manufacturers use our product as a core reagent in the synthesis of selected thiourea-based herbicides and fungicides. It reacts with amines and other nucleophiles under controlled alkaline or solvent-free conditions, facilitating the formation of active urea and carbamate pesticide intermediates. Batch reaction conditions require precise addition and containment, given the compound’s reactivity and vapor pressure. Integration into multi-step synthesis increases throughput, with monitoring for release limits and occupational exposure.

    Industry compliance standards

    • European REACH Regulation (EC) No 1907/2006 for precursor handling
    • ISO 9001:2015 for quality management of agrochemical inputs
    • Guidelines for environmentally sound management of pesticide intermediates (FAO/WHO)
    • US EPA Pesticide Registration standards for raw material traceability

    Typical usage ratio

    • 0.7–1.2 equivalents, depending on nucleophile reactivity and process scale
    • Usage ratio adjusted to upstream purity and targeted product yield; process R&D confirms stoichiometry

    Downstream process integration

    • Continuous or semi-batch addition during thiourea/urea formation
    • Direct charging into jacketed reactors under nitrogen
    • Controlled temperature escalation with condenser-line gas scrubbing
    • Downstream separation by liquid-liquid extraction and purification

    Final product types

    • Selective pre-emergent herbicide actives
    • Systemic fungicide precursors
    • Intermediate for sulfonylurea weed control agents
    • Custom thiocarbamate pesticides

    2. Pharmaceutical API Intermediate Synthesis

    Our material supports pharmaceutical companies manufacturing intermediates for anti-cancer and anti-hypertensive APIs containing isothiocyanate functional groups. Controlled nucleophilic substitution enables precise introduction into heterocyclic frameworks or aromatic amines during small-molecule API synthesis. Manufacturing follows GMP alignment and necessitates validated impurity control, process documentation, and in-process QC at each coupling stage. Handling protocols address both operator safety and cross-contamination prevention.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 for raw material receipt and testing
    • US FDA 21 CFR Parts 210 and 211 for excipient and intermediate management
    • EDQM monograph reference when isothiocyanate-derived intermediates are pharmacopoeial

    Typical usage ratio

    • 0.9–1.1 molar equivalents versus coupling partner
    • Precise stoichiometry set by synthesis route validation; minor excess used to ensure full conversion in certain steps

    Downstream process integration

    • Pre-dissolution in approved solvents (e.g., acetonitrile, DMF) before addition to reaction vessel
    • Charged during mid-stage or late-stage heterocyclization or side-chain installation
    • Subject to multi-step purification post-reaction (crystallization, HPLC)
    • Retention samples collected for regulatory filing batches

    Final product types

    • Intermediates for anti-cancer agent synthesis (e.g., thiourea-linked kinase inhibitors)
    • Building blocks for anti-hypertensive drugs (e.g., sulfonylurea core intermediates)
    • Precursors for active heterocyclic pharma compounds
    • Analytical standard production for pharma QC

    3. Rubber Chemical Accelerators

    Rubber manufacturers apply our material in the controlled synthesis of certain thiourea and dithiocarbamate-based accelerators, which drive vulcanization kinetics in specialty elastomers. This use involves reaction with secondary amines or base-treated alcohols, followed by structural modification. End users require narrow specification on sulfur and nitrogen content for downstream predictability in tire, hose, or industrial rubber part fabrication.

    Industry compliance standards

    • ISO 9001:2015 for consistent accelerator batch quality
    • ASTM D4671 for compounding material identification
    • REACH SVHC assessment for downstream rubber articles
    • Chinese GB/T 21880 for accelerator classification in rubber industry

    Typical usage ratio

    • 5–10% by weight of the final accelerator formulation
    • Exact ratio adapted to the vulcanization profile and elastomer type

    Downstream process integration

    • Introduced in pre-mix or main kneading of accelerator synthesis
    • Reacted at 50–80°C under inert conditions, prior to blending with base polymers
    • Quality tested for ash content, residue, and accelerative efficiency
    • Final accelerator dust-controlled for safe handling

    Final product types

    • Rubber vulcanization accelerators
    • Dithiocarbamate formulation aids
    • Specialty rubber modifiers
    • Rubber compound masterbatches

    4. Advanced Organic Synthesis for Specialty Chemicals

    Chemical research companies and fine chemical producers use ethyl isothiocyanate for customized synthesis of organosulfur and heterocyclic specialty compounds. The material enters as an electrophilic isothiocyanate reagent, often under Schotten–Baumann or catalytic conditions, supporting a range of tailored reactions including ligation, cyclization, and group transfer. Applications demand high-purity inputs, detailed MSDS, and batch traceability, with rigorous documentation for customer-specific process audits.

    Industry compliance standards

    • ISO 9001:2015 for fine chemicals and intermediates
    • Responsible Care chemical management protocols
    • Custom synthesis agreements specifying starting material purity (≥98%)
    • EU CLP Regulation 1272/2008 for substance labeling

    Typical usage ratio

    • 1:1 molar ratio for most ligation and cyclization reactions
    • Adjusted upward by up to 15% in multi-component or yield-critical synthesis

    Downstream process integration

    • Feedstock charged under inert gas for moisture-sensitive protocols
    • Used during early- or mid-stage synthesis for group transfer
    • Reaction byproducts neutralized and separated before final purification
    • Full batch traceability maintained for regulated customer supply chains

    Final product types

    • Sulfur-containing fine chemicals
    • Heterocyclic molecule precursors
    • Pre-functionalized specialty ligands
    • Advanced research intermediates

    5. Plastics Additives and Modifier Production

    Specialty plastics producers use our ethyl isothiocyanate in manufacturing selected nucleating agents and crosslinkers for thermoplastic and thermoset resin systems. The isothiocyanate group allows precise modification of polymer microstructure or acts as a reactive crosslinker during extrusion, compounding, or batch molding. Each process stage demands fixed impurity limits and in-line monitoring of residuals to comply with international polymer additive standards.

    Industry compliance standards

    • ISO 9001:2015 for specialty additive input QA
    • EU Regulation (EU) No 10/2011 on plastic materials & articles intended for food contact (where applicable)
    • US FDA 21 CFR 177.1520 for polymer additive use in food contact plastics (where applicable)
    • ASTM D2563 for plastics compound composition

    Typical usage ratio

    • 0.05–0.2% by weight in plastic formulation, referenced to polymer mass
    • Ratio optimized based on required crosslinking density and additive compatibility

    Downstream process integration

    • Metered dosing during extrusion or compounding
    • Solution-phase or melt-phase mixing with base resin
    • Reactive incorporation during crosslinking stage at elevated temperature
    • Final plastics tested for extractables and residuals per customer protocol

    Final product types

    • Thermoplastic polyolefin modifiers
    • Nucleating agents for injection molding
    • Specialty crosslinked plastics
    • Functional polymeric additives for engineering plastics
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