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Trichloroacetonitrile

    • Product Name Trichloroacetonitrile
    • Alias Cyanotrichloromethane
    • Einecs 210-772-0
    • 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

    606374

    Cas Number 545-06-2
    Iupac Name Trichloroacetonitrile
    Molecular Formula C2Cl3N
    Molar Mass 128.39 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.44 g/cm³
    Boiling Point 83-84 °C
    Melting Point -42 °C
    Solubility In Water Reacts with water
    Flash Point 44 °C (closed cup)
    Refractive Index 1.434 at 20 °C
    Odor Pungent
    Vapor Pressure 33 mmHg at 25 °C

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

    Packing & Storage
    Packing A 100 mL amber glass bottle with a secure screw cap, labeled "Trichloroacetonitrile, CAS 545-06-2, hazardous—handle with care."
    Shipping Trichloroacetonitrile should be shipped in tightly sealed containers, away from moisture, heat, and incompatible substances, in accordance with local, national, and international regulations. It is classified as a hazardous material (UN2683), requiring labeling and documentation for toxic substances, and should be handled only by trained personnel during transportation.
    Storage Trichloroacetonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect it from moisture, sunlight, and sources of ignition. Store in a corrosion-resistant container with a resistant inner liner. Clearly label the storage area and follow all regulatory and safety guidelines for hazardous chemicals.
    Application of Trichloroacetonitrile

    Applications of Trichloroacetonitrile in Industrial Manufacturing

    As a direct manufacturer of trichloroacetonitrile, we provide this specialty organic intermediate to enable high-value transformations across select chemical sectors. We support customers in each industry with technical guidance for process integration, compliance, and formulation control, based on commercial production experience at scale. Below are core downstream segments where trichloroacetonitrile has established, regulated roles in industrial manufacturing workflows.

    1. Crop Protection Synthesis — Pesticide and Herbicide Active Ingredients

    Trichloroacetonitrile serves as a chlorinating and cyanating intermediate in the synthesis of various heterocyclic compounds, including triazine-based and pyridazine-based pesticides. Agrochemical manufacturers introduce this material during critical cyclization or condensation steps to enable functional group transformations needed for active ingredient structures. Formulation chemists adjust the dosage based on final product target molecules and catalytic requirements, maintaining batch traceability for regulatory and process audits. End products include selective herbicides and fungicides for both pre- and post-emergence field applications.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • China GB 2763 Maximum Residue Limits

    Typical usage ratio

    • 0.5–3.5 molar equivalents per target synthesis, depending on substrate and pathway

    Downstream process integration

    • Reactant for heterocycle ring closure during multi-step synthesis of triazines and pyridazines
    • Introduced post-hydrolysis or amidation, under controlled temperature and nitrogen atmosphere

    Final product types

    • S-triazine herbicides (e.g., atrazine, simazine)
    • Pyridazine fungicides
    • Intermediate blends for downstream formulation into emulsifiable concentrates and suspension concentrates

    2. Pharmaceutical Intermediate — API Side Chain Building Blocks

    In regulated pharmaceutical manufacture, trichloroacetonitrile enables key transformations for complex drug intermediates, including nitrile insertion or halogenation steps essential for side chain modification or activation. It plays a role in alkylation reactions and in introducing trichloromethyl groups, supporting the synthesis of certain nucleoside analogues and other APIs under stringent cGMP protocols. Handling protocols and dosing strategies depend on the targeted impurity profile and reaction pathway, with all inputs batch-documented for regulatory traceability.

    Industry compliance standards

    • ICH Q7 Guidelines for Active Pharmaceutical Ingredient Production
    • US FDA 21 CFR Part 210, 211
    • European Pharmacopoeia (Ph. Eur.)
    • Good Manufacturing Practice (GMP) compliance

    Typical usage ratio

    • 0.2–1.2 molar equivalents relative to precursor substrate; typically adjusted to prevent over-halogenation or nitrile migration based on validated batch records

    Downstream process integration

    • Alkylation or nitrile introduction during side chain synthesis or functional group activation for small molecule APIs
    • Added in closed reactor systems with in-line QC monitoring

    Final product types

    • Nucleoside analogues (precursor stage)
    • API intermediates for antiviral and oncology drugs
    • Custom building blocks for CDMO production lines

    3. Dyestuff Manufacturing — Cyanuric and Reactive Dye Precursors

    Dyestuff producers use trichloroacetonitrile strategically in the manufacturing of triazine-based reactive dye intermediates. Its reactivity facilitates the stepwise introduction of reactive chlorines, enabling formation of cyanuric chloride from cyanuric acid pathways. These intermediates then anchor dye molecules or functionalize dye bases for higher covalent bonding with cellulose substrates. Formulation concentration of trichloroacetonitrile depends on targeted mono/di/trichloro substitution and batch size, maintained within plant emission and worker safety limits.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 for restricted chemicals
    • REACH Regulation (EC) No 1907/2006
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001 for process and documentation controls

    Typical usage ratio

    • 0.6–2.5 molar equivalents per triazine core, optimized by degree of substitution

    Downstream process integration

    • Chlorination step following cyanuric acid formation; typically executed in jacketed reactors with chlorine / trichloroacetonitrile co-feed

    Final product types

    • Cyanuric chloride
    • Monochlorotriazine dye bases
    • Bifunctional and monofunctional reactive dyes for cellulose and wool applications

    4. Organic Synthesis for Fine Chemical Intermediates

    Chemical processing plants utilize trichloroacetonitrile as a reactive intermediate for the preparation of specialty compounds, such as substituted acetonitriles, amidines, and trichloromethylated aromatics. This enables production of tailored intermediates used in polymer additives, photoinitiators, and specialty resin curing agents. Formulators determine addition rates based on substrate reactivity and downstream purification methods, critically controlling temperature and pH to maximize selectivity and minimize by-product formation during synthesis campaigns.

    Industry compliance standards

    • ISO 14001 Environmental Management for emissions control
    • Custom specification agreements with downstream OEMs
    • Internal QC based on in-house validated HPLC/GC protocols

    Typical usage ratio

    • 1.0–4.0 molar equivalents, as determined by substrate availability and target group transformation in route design

    Downstream process integration

    • Stepwise addition in controlled batch or continuous reactors during intermediate construction, often after halogen exchange or amination steps

    Final product types

    • Photoinitiator precursors
    • Custom amidine derivatives
    • Polymer performance additive intermediates

    5. Specialty Chemical Manufacturing — Halogenated Solvent Component

    Manufacturers within the specialty chemical sector employ trichloroacetonitrile as a precursor in the formulation of halogenated solvent blends for extraction, reaction media, or as phase transfer additives in multi-phase organic syntheses. It may also be used for the in-situ generation of atypical halogenated functional groups during fluorine or chlorine atom exchange. Integration and percentage depend on solvent system design and desired substrate solubility improvement, while meeting stringent safety and emissions standards.

    Industry compliance standards

    • EU CLP Regulation (1272/2008) for solvent classification and labeling
    • OSHA Process Safety Management (USA, 29 CFR 1910.119)
    • National Fire Protection Association (NFPA) codes for halogenated mixtures

    Typical usage ratio

    • 1–10% by volume in custom halogenated solvent systems; adjusted based on solvent miscibility and target application

    Downstream process integration

    • Blended as a minor phase component in batch mixing tanks, with real-time sensor monitoring for vapor containment

    Final product types

    • Extraction solvents for fine chemical separations
    • Phase transfer media for laboratory and pilot scale organic synthesis
    • Solvent blends for electronics and dry process cleaning formulations
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    Certification & Compliance
    More Introduction

    Introducing Trichloroacetonitrile: A Fundamental Building Block in Fine Chemicals Manufacturing

    The Role of Trichloroacetonitrile in Today’s Chemical Industry

    Coming from years of hands-on production, we see clear advantages in Trichloroacetonitrile (TCAN), both for its reactivity and its compatibility with a range of chemical synthesis routes. Our typical product specification focuses on high purity, often not less than 99%, with stringent control over trace impurities like moisture and related chlorinated byproducts, which we continually monitor by gas chromatography. Every batch is carefully sampled and tested before dispatch, a practice built from over a decade of manufacturing experience and repeated customer feedback.

    In the broader chemical space, TCAN looks simple at first glance—little more than a compact molecule with three chlorine atoms and a nitrile group. Its utility grows out of that structure: it brings high electrophilicity and strong halogenation, offering a unique combination that drives selective transformations. As chemists, we keep seeing it in custom manufacturing, pharmaceuticals, and agrochemicals—especially where conversions like chlorination, dehydration, or cyanation matter.

    Product Model and Packaging

    Customers often ask for clear guidance on packaging. Standard models leave little room for ambiguity. We work primarily with bulk liquid grades, supplied in steel drums or IBC tanks lined for halogenated compounds, tailored to secure transportation and extended storage. Each container’s fill volume aligns with international recommendations for safety and environmental responsibility; our experience demonstrates that this reduces the risk of leaks when bulk-shipped overland or by sea.

    Our process engineers design quality checkpoints at every stage, starting from raw material sourcing. Chlorine and acetonitrile, the key feedstocks, are reaction-controlled under anhydrous conditions. We run continuous monitoring for exothermicity and reaction rates—safety and yield both demand it. We tailor each production lot to the needs expressed directly by formulators and synthetic chemists, many of whom visit for joint process trials. We do not offer repackaged or diluted stocks: our site stands behind everything shipped.

    Comparing Trichloroacetonitrile with Analogous Chemicals

    TCAN stands apart from lighter chlorinated nitriles and trichloroacetic derivatives. Deeper chlorination such as tetrachloroacetonitrile alters both volatility and reactivity, pushing the compound out of the optimal range for most dehydrative coupling or nucleophilic substitution applications. Difluoro or dichloro analogues, while interesting for some niche transformations, rarely hit the balance of reactivity, purity margin, and manageable volatility that TCAN consistently provides.

    Unlike more volatile chlorinated solvents that sometimes escape containment or present greater inhalation hazards, Trichloroacetonitrile’s boiling point keeps vapor pressure at workable levels at room temperature. This reduces health risk to operators and researchers working in less-than-perfect ventilation. Some partners share stories about switching from carbon tetrachloride or chloroform due to stricter regulations on ozone-depleting substances; TCAN offers a viable route away from these problematic materials while maintaining direct compatibility with common reaction protocols.

    Nitriles distinguish themselves in synthesis by introducing an active ‘–CN’ group. Where Trichloroacetonitrile departs from basic acetonitrile or cyanogen chloride is in the balance between reactivity and selectivity. This balance allows chemists to drive chlorine-based transformations or cyanation reactions without exposing themselves to the far higher volatility and acute toxicity of cyanogen chloride. Our on-site health and safety team, working closely with researchers, confirms repeatedly how this difference has directly benefited plant workers during scale-ups and prolonged handling.

    Applications: Experience Drives Innovation

    Our largest volume of Trichloroacetonitrile flows directly toward herbicide and pesticide intermediate production, where its trichloromethyl group serves as a launching point for specialty transformation steps. The pharmaceutical sector values its fit as both a reagent and a coupling partner, especially in constructing key intermediates for complex API (Active Pharmaceutical Ingredient) syntheses. In high-throughput sites, speed and selectivity become decisive factors for route selection; we regularly conduct joint trials to validate that our TCAN supports customers’ process targets.

    Specialty plastics producers experiment with TCAN as a halogen source in polymer backbone modifications, often searching for higher resistance to thermal breakdown or customized solubility profiles. Synthetic chemists in research settings employ it for quick introduction of halogenated functional groups—critical for modulating activity or binding affinity in final molecules. Across these segments, we see a common pattern: once process chemists validate Trichloroacetonitrile at lab scale, they integrate it into production quickly because it sidesteps known issues with impure feedstocks or unpredictable moisture content found in less strictly made chemicals.

    Sometimes, we see demand for custom grades—where trace water content or residual monochlorinated impurities must be pushed even lower than standard. Our in-house team uses fractional distillation and specialized drying to reach specifications well beneath standard industry minimums, documented by comprehensive lab analytics. We base adjustments on feedback from downstream users who notice even slight variances in reactivity or byproduct formation. These are real-world challenges, not hypothetical claims.

    Lessons Learned: Addressing Challenges

    Shipping trichlorinated organic chemicals involves more than paperwork and regulatory filings. Leak containment, operator training, and proper PPE matter most on the ground. Even a minor equipment failure in the transfer system can trigger rapid evacuation and require months to rebuild trust with an overseas partner. Years of logistics teach us direct communication with supply chain partners keeps all sides safer—advising on container selection, temperature limits, and handling protocols.

    Years back, a severe storm delayed a bulk shipment mid-transit. The extended hold risked temperature increases inside the drums, pushing vapor pressure beyond safe levels. This real episode forced us to develop new guidance for thermal limits and contingency plans—for both storage on arrival and transport over land. Now, our logistics teams follow real-time weather and port conditions; they hold the authority to reroute or stagger shipments to match risk ratings. These tactics grew from lessons others might skip over in textbooks but prove critical to reliability.

    Upstream and Downstream: Managing Quality from Start to Finish

    Careful feedstock selection impacts final TCAN quality. We source chlorine under long-term contracts directly tied to purity thresholds, with on-site chlorine generators as backup. Acetonitrile enters double-tested by both supplier certification and our lab, particularly for peroxide, residual water, or lower nitrile contaminants. These steps precede any synthesis run and have become routine after earlier issues: unexpected peroxide spikes once forced whole-lot recalls, teaching us the hard way.

    On the tail end, we set up returnable drums under traceable tracking codes, encouraging partners to return empty packaging for both safety and recycling. Explaining drum rinsing and safe venting isn’t only a regulatory check-box; it stops accidental byproduct formation and keeps operator exposure lower. We prefer these rigorous measures because dangerous waste events don’t just pose fines—they damage reputations built over decades.

    Regulation, Safety, and Responsible Handling

    Trichloroacetonitrile manufacturing involves strict compliance with chemical plant process safety regulations, both domestic and international. We partner with accredited testing labs for yearly hazard audits and keep open dialogue with environmental monitoring bureaus. Internal training cycles revisit emergency drills, backed by real incident data. We do this not from obligation but because failures in this sector linger: one contamination event can close a facility for months.

    Operators involved in drum filling, pumping, and sampling use full-face respirators and chemically resistant clothing. Early in our operations, we observed that partial PPE regimes contributed to minor irritations; complete protection eliminated these events over time. We share these observations during plant tours, recommending suppliers and customers establish similar standards at their own facilities.

    Disposal involves more than dilution or landfill. We recover residuals from containers and encourage downstream incineration under high-temperature, scrubbed conditions. Local communities review our emissions data at quarterly open houses—transparency strengthens acceptance, and we value their input in improving site practices.

    Looking Forward: Supporting Sustainable Chemistry

    The field continues to evolve. We keep searching for cleaner reaction systems for preparing Trichloroacetonitrile, especially with less need for chlorinated solvent media. Friends in green chemistry circles discuss biodegradable alternatives and nonchlorinated nitrile sources, but few offer the performance traits that current TCAN brings to synthesis scale. Our R&D invests in lower temperature reaction routes, aiming to lower energy consumption and waste. Pilot projects analyze new filtration media for byproduct removal, cutting cycle time and improving margin on clean runs.

    In dialogue with academic partners, we see research heading toward milder alternative catalysts and real-time reaction monitoring. We run side-by-side tests comparing new variants with our mainline TCAN, always refining our process to lower both environmental and operator risk. It takes discipline to reject unproven shortcuts; sticking to protocols honed by years of factory practice prevents mistakes that could cost both business and goodwill.

    Why Trichloroacetonitrile Remains Important

    Few chemicals match the versatility or process fit of Trichloroacetonitrile in the sectors we serve. It holds its ground against both legacy and next-wave fine chemical intermediates, producing consistent results batch after batch. Years on the production floor confirm that stable sourcing, rigorous analytics, and open channels to users make the crucial difference—lab data matter, but real-world feedback ties theory to practice.

    Many buyers are tempted toward cut price imports or diluted alternatives. Our experience—backed by direct evidence—shows the cost of handling off-spec shipments and production interruptions always outweighs the savings. We learned to focus on fundamentals: purity, reactivity, manageable volatility, predictable regulatory status, and reliable delivery. Those priorities, proven in both routine runs and stress scenarios, underpin the trust that repeats year after year.

    We welcome questions—from the lab bench to the loading dock. Only by maintaining an open, exchange-based relationship with partners and users do we keep raising standards. Direct feedback from skilled chemists and plant technicians improves our next generation batches. This continuous, experience-based cycle of improvement gives the market chemicals that support the ambitions of scientific teams worldwide—something no datasheet can ever fully replace.