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2-Chloro-5-Trifluoromethylbenzyl Chloride

    • Product Name 2-Chloro-5-Trifluoromethylbenzyl Chloride
    • Alias Benzyl chloride, 2-chloro-5-(trifluoromethyl)-
    • Einecs 228-272-4
    • 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

    407230

    Product Name 2-Chloro-5-Trifluoromethylbenzyl Chloride
    Cas Number 86604-75-7
    Molecular Formula C8H5Cl2F3
    Molecular Weight 229.03
    Appearance Colorless to pale yellow liquid
    Boiling Point 219-221°C
    Density 1.395 g/cm³
    Purity Typically ≥98%
    Refractive Index n20/D 1.523
    Flash Point 97°C
    Solubility Insoluble in water; soluble in organic solvents
    Storage Conditions Store at room temperature, keep tightly closed

    As an accredited 2-Chloro-5-Trifluoromethylbenzyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Chloro-5-Trifluoromethylbenzyl Chloride is supplied in a 25g amber glass bottle, sealed, and labeled with hazard information.
    Shipping **Shipping Description:** 2-Chloro-5-Trifluoromethylbenzyl Chloride is shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. Classified as a hazardous material, it must be transported according to local and international regulations. Proper labeling, protective packaging, and documentation are required to ensure safe handling and prevent leaks or environmental exposure during transit.
    Storage 2-Chloro-5-Trifluoromethylbenzyl Chloride should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from sources of ignition and heat. Protect it from moisture and direct sunlight. Keep separate from incompatible substances such as strong oxidizers or bases. Ensure proper labelling and access only to trained personnel, following relevant safety regulations.
    Application of 2-Chloro-5-Trifluoromethylbenzyl Chloride

    Applications of 2-Chloro-5-Trifluoromethylbenzyl Chloride in Industrial Manufacturing

    2-Chloro-5-Trifluoromethylbenzyl Chloride is a specialized halogenated aromatic intermediate primarily leveraged by regulated industrial sectors for the synthesis of advanced fine chemicals. As a manufacturer with extensive experience in downstream cooperation, we supply this material to high-value application fields with controlled supply chains, where traceability and consistency are critical for final product performance and regulatory approval. Below, we detail key application scenarios grounded in our direct customer feedback and documented end-uses.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Antiviral and Antihypertensive Intermediates

    Pharmaceutical companies employ our product in multi-stage synthesis as a functionalized benzyl halide for the preparation of intermediates found in certain antiviral and antihypertensive APIs. The presence of the trifluoromethyl and chloro moieties enables selective substitution and protection strategies, which are vital for constructing molecular backbones with required biological activity. This material typically enters the process during late-stage functionalization, where precise impurity control and reaction monitoring ensure pharmaceutical-grade output.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 210/211
    • European Pharmacopoeia (Ph. Eur.) reference standards
    • Chinese Pharmacopoeia (ChP) guideline for API intermediates

    Typical usage ratio

    • Applied at 0.92–1.12 molar equivalents relative to the next reactant; operators adjust based on monitoring for unreacted starting material and target intermediate yield

    Downstream process integration

    • Used in controlled halogenation or nucleophilic substitution during API intermediate formation, preceding purification and chiral resolution steps

    Final product types

    • Intermediates for oral antivirals and select antihypertensive actives (e.g., Angiotensin II receptor antagonist pre-cursors)

    2. Agrochemical Synthesis: Advanced Herbicide Building Blocks

    Leading agrochemical formulators integrate this material within synthesis routes for special-purpose herbicide and fungicide molecules, benefitting from the electron-withdrawing properties that improve compound stability and enhance target specificity. The compound enters the process at pre-conjugation or halogen-exchange stages, directly shaping the scaffolding of proprietary fungicide or herbicide molecules designed for regulated crop applications.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • EU REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • OECD Guidelines for the Testing of Chemicals (relevant for active ingredients)
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • Utilized at 0.9–1.1 equivalents by molecule design, adjusted to minimize waste and optimize active ingredient yield before further downstream derivatization

    Downstream process integration

    • Introduced during functional group formation or active core modification prior to final formulation and encapsulation of crop protection agents

    Final product types

    • Herbicide actives for grain and oilseed protection
    • Precursor for systemic fungicides used in high-value crops

    3. Specialty Polymer Modifiers: High-Performance Fluorinated Resins

    Polymer manufacturers utilize this raw material as a reactive modifier for advanced aromatic resins, imparting hydrophobic and chemical-resistant characteristics essential for performance coatings and engineered plastics. The strong electron-withdrawing substituents enable controlled grafting onto aromatic polymer chains during polymerization or post-polymer functionalization, generating specialty resins demanded by electronics and industrial coating suppliers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • EU RoHS Directive (2011/65/EU)
    • UL 94 Flammability Standard for Plastics Materials
    • ASTM D543 Chemical Resistance of Plastics

    Typical usage ratio

    • Commonly 0.5–3.0 wt% by total monomer/resin mass, adjusted according to the balance of mechanical properties and chemical inertness required in the final matrix

    Downstream process integration

    • Fed into polymerization reactor as a functional monomer or used in secondary functionalization of pre-formed resins prior to extrusion and molding

    Final product types

    • Fluorinated resin coatings for electronic device housings
    • Specialty plastic films and sheets
    • Protective polymer overcoats for industrial equipment

    4. Fine Chemical Manufacturing: Liquid Crystal and OLED Intermediate Synthesis

    Manufacturers in the optoelectronics sector rely on this material as a specialized intermediate for creating custom fluorinated aromatic compounds that regulate molecular alignment and electron mobility in advanced display technologies. By introducing this building block at controlled stages, process engineers achieve high-purity intermediates required for the assembly of high-performance liquid crystals and OLED emissive/charge-transport layers.

    Industry compliance standards

    • ISO 14001 Environmental Management (for chemical synthesis facilities)
    • IEC 61340-5-1 Electrostatics (relevant for electronic chemicals)
    • JPCA-ES-01 Environmental and Safety Standard (Japan Electronics Packaging and Circuits Association)
    • RoHS-compliance for final component use

    Typical usage ratio

    • 1.0–1.5 molar equivalents, tuned to match the downstream target fluorophenyl or polyaromatic system; precision batch tracking during scale-up

    Downstream process integration

    • Employed in arylation or halogen exchange reactions within organic syntheses, directly yielding reactive intermediates for device-grade chemical purification

    Final product types

    • Fluorinated aromatic intermediates for TFT-LCD alignment layers
    • OLED intermediate chemicals for emissive layer formation

    5. Veterinary Pharmaceutical Intermediate Manufacturing

    Producers of veterinary active substances adopt this intermediate within routes for new-generation veterinary drugs intended for livestock and companion animal health. Here, strict process validation accompanies each batch to confirm the identity and absence of genotoxic impurities, and the intermediate is introduced via targeted halogenation or coupling steps before API finalization and formulation.

    Industry compliance standards

    • VICH GL Manufacturing Guidance
    • US FDA Guidance for Industry: Veterinary Drug Residue
    • European Medicines Agency (EMA) Quality of Veterinary Medicinal Products
    • Chinese Veterinary Pharmacopoeia

    Typical usage ratio

    • Used at 0.95–1.10 molar ratio in alignment with target animal drug synthesis schemes; ratio validated by reaction completion and product isolation stage

    Downstream process integration

    • Functionalized in late-stage coupling or protective group strategies, followed by hydrolysis and refinement to yield final veterinary actives

    Final product types

    • Antiparasitic and anti-infective veterinary actives
    • Intermediate compounds for veterinarian-use tablets and injectables
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    Certification & Compliance
    More Introduction

    2-Chloro-5-Trifluoromethylbenzyl Chloride: From Synthesis to Application

    Understanding Our Product from the Factory Floor

    After years of working daily with 2-Chloro-5-Trifluoromethylbenzyl Chloride and handling every step from raw materials to finished product, we can say this—producing such a compound requires continuous attention to detail. Its chemical structure, featuring a chloro and trifluoromethyl group on a benzyl chloride backbone, gives it unique reactivity. Consistency stands out as the first result of deep familiarity during manufacturing, and our workflow reflects this reality. Starting with chloroacetylation and careful control of temperature at each stage, we maximize yield and minimize byproducts. Batch after batch, purity matters because small changes in ratio make sizable differences in how the product behaves downstream.

    We produce this material for customers who need reliability, usually in pharmaceutical synthesis, agrochemical intermediates, and advanced materials labs. We stick to liquid form with a pale-yellow appearance, recognizing how small contamination shows up right away both visually and by GC assay. Our lab runs regular chromatography and NMR analysis to verify content above 99%, and if it dips, the whole lot stays put until we correct the issue. This insistence comes from years facing rework and loss from even the tiniest trace of water or a variation in trifluoromethyl placement.

    Specifications, but Not by Template

    As working chemists, we think less about the spec sheet and more about what practical differences arise during synthesis or scale-up. Our batches feature a narrow purity window, since trace impurities interfere with downstream nucleophilic substitutions and coupling reactions. Water sensitivity can hold back lab progress, so we pass each lot through a tight drying process, using distillation instead of simple evaporation. This step often separates quality producers from those who just push product down the line.

    By experience, many partners prefer containers that minimize surface interactions and vapor loss. For this, we use lined drums with strong seals. If a customer needs smaller aliquots, we offer ampoules or bottles, always packed with nitrogen to keep air and water vapor away. While most recognize assay above 99% as standard, we actually run additional tests for key trace halides and difluorinated benzylic byproducts, aiming for tighter impurity profiles, especially for late-stage pharmaceutical precursors.

    Manufacturing Differences Set Us Apart

    From the outside, one bottle can look similar to the next. Inside, complexity piles up, starting from the choice of catalyst during synthesis. Chlorination steps performed at higher temperatures often produce more unwanted side products. We optimize synthesis using a milder catalytic process, keeping yields high and impurity burdens low. It’s tempting to run hotter and faster for volume, but this leads to more spent solvent and problem batches.

    We’ve seen how handling and storage change product stability. Even with a closed system, the wrong kind of packaging or a slightly basic environment causes hydrolysis and forms unwanted benzylic alcohols. We store and ship under inert gas. Regular shelf-life testing gives real data about degradation, so customers see the same material at their bench as we see on ours.

    Unlike generic suppliers, we manufacture lots that are traceable back to each production run. Every small deviation—from raw stock molarity to temperature ramp rates—gets logged, and we adjust our process recipes in real time. If a process batch shows high halide residuals, we halt and rework instead of passing along risk. The kind of control built into our systems shows up down the road in less downtime and fewer surprises for chemists.

    What Sets 2-Chloro-5-Trifluoromethylbenzyl Chloride Apart

    From our viewpoint as direct manufacturers, the distinction emerges in processability and final purity. Many analogous benzyl chlorides show sluggishness in benzylic substitution reactions, especially with steric hindrance. The trifluoromethyl group in our product activates the benzyl position, supporting cleaner and faster reactions. Experienced synthetic chemists see this in higher isolated yields and fewer purification steps required after coupling or substitution. When using other products, we notice longer reaction times and more residual starting material in the crude product.

    This compound serves as a key intermediate when building complex molecules in the pharmaceutical and agrochemical fields. For example, in developing active ingredients for herbicides or certain antifungal agents, our customers use this molecule as a platform for attaching various functional groups. The electron-withdrawing effect from both chloro and trifluoromethyl enhances selectivity during these steps, supporting fewer side reactions and more robust yields.

    From Factory Lab to Customer Synthesis

    Quality doesn’t happen from last-minute fixes or quick tests. Each production run starts with a fresh review of previous outcomes. If a column chromatography report reveals trace ether contamination or higher-than-planned residual solvents, we tweak parameters on that very next cycle. Sampling points along the line mean problems get caught at every stage before bulk filling.

    Shipment and storage present their own risks. We keep the product away from moisture, direct light, and reactive materials from the start. Where some operations bulk fill with little oversight, our staff verifies each drum for weight, seal integrity, and internal pressure before it moves to storage. Unexpected results on shipping QA get traced back to their production date, and, if necessary, the lot is held for retesting.

    We’ve responded to customers who once saw variable performance when sourcing this compound from multiple vendors. Some encountered incomplete conversion or strange byproducts during palladium-catalyzed reactions, only to discover their supplier’s product contained residual non-fluorinated benzyl chlorides. We offer open data on impurity profiles—not just the minimum standard spec. Our approach stems from direct conversations with frustrated chemists and production managers who need the same quality from one pail to the next.

    Uses Informed by Hands-On Experience

    2-Chloro-5-Trifluoromethylbenzyl Chloride shows up most often in synthetic steps requiring a selective and reactive benzylating agent. We see our largest users creating APIs or testing new agrochemicals. The product’s unique reactivity comes from the electron-withdrawing nature of the trifluoromethyl and chloro groups, making the benzylic chloride more susceptible to nucleophilic attack.

    We’ve manned production lines where even a small impurity alters the coupling yield, especially for customers using complex, multi-step procedures. In house, we sometimes push downstream reactions—aminations, etherifications, and thioetherifications—to pressure-test real use scenarios. The difference between high-purity and slightly off-spec material often shows in catalyst fouling and required purification effort. Recalls and failed reactions are not just inconvenience; in regulated sectors, they slow development timelines by weeks or months.

    Some customers use this compound to attach specialty chains for liquid crystals or as a building block for fluorinated polymers. In each case, the subtle reactivity, driven by the placement of the trifluoromethyl group, supports a broader range of synthetic outcomes. By drawing on decades at the bench, we recognize just how much small changes in manufacturing impact process chemistry and final application.

    Comparative Perspective on Related Chemicals

    Compared to standard benzyl chlorides without heavy halogen or fluorine substitution, 2-Chloro-5-Trifluoromethylbenzyl Chloride offers distinct reaction profiles. During pilot runs with non-fluorinated analogs, side reactions increased and finished product purity suffered. The electron-withdrawing properties of trifluoromethyl and chlorine groups create new possibilities for selectivity and activation not seen in plain benzyl chlorides.

    We have seen some users try to substitute with less expensive, lightly halogenated benzyl chlorides. Often, these led to batch process headaches like incomplete conversions and higher isolation costs. As actual manufacturers who have handled these alternatives side by side, we know firsthand that small chemical differences at the molecular level cause measurable headaches for industrial chemists aiming for predictable, scalable synthesis.

    Beyond simple purity or reactivity points, our product’s impurity profile proves critical. Competing suppliers sometimes accept higher levels of mixed halide byproducts, assuming downstream users won’t notice. In regulated industries—especially pharma—trace side products mean a world of lost time and additional validation. Our commitment to deeper testing, redundant purification, and continuous batch tracking goes well beyond a book spec.

    Challenges and Real-World Solutions

    Handling and distributing reactive halides poses real challenges, both in the plant and in the end user’s lab. From blocked transfer lines to label degradation from off-gassing, problems show up when container compatibility isn’t prioritized. We partner directly with drum and bottle manufacturers to develop inert lining solutions, and we select packaging based on our own in-house stress tests over months, not just days.

    Contamination prevention demands diligence; the slightest water ingress or reactive oxygen source starts a chain of hydrolysis and product breakdown. To address this challenge, we built dedicated lines that never handle incompatible compounds and perform transfer operations exclusively under dry, inert atmospheres. Results show up in fewer rejected lots and more consistent outcomes for customers.

    We have also learned the importance of regulatory compliance not just for shipment, but during every stage of production. This means sourcing raw materials from known, audited suppliers, repeatedly analyzing each incoming shipment for purity and conformance, and building full traceability down to ingredient batch. The extra work at the outset minimizes risk of downstream regulatory scrutiny. It also gives our customers confidence that every delivered batch meets not only contractual, but ethical and regulatory standards.

    Looking Forward: Responsible Manufacturing and Innovation

    Our ethos as a chemical manufacturer keeps us focused on incremental, evidence-based improvements instead of chasing flash-in-the-pan process tricks. It comes down to investing in our people, keeping the plant clean, and listening openly to both customer feedback and regulatory updates. In the past, we adapted our drying protocols after learning from a pharmaceutical customer how even fractional water contamination in the product stream resulted in lost yield during late-stage alkylation. Based on their real feedback and our own analysis, we installed additional inline drying columns and extended atmospheric monitoring.

    We maintain a rotating sample retention system with regular re-analysis to ensure product integrity over longer-term storage. This allows us to spot slow-developing stability issues and adapt future runs well before end users experience product drift. In a sector where customer timelines depend on reliable and consistent supply, this attention to long-term stability pays dividends.

    Innovation in manufacturing isn’t just introducing new raw materials or swapping catalysts. It’s also about better analytics, more reliable process control, and a willingness to pause for reevaluation. For 2-Chloro-5-Trifluoromethylbenzyl Chloride, these ongoing improvements support both small-scale R&D labs and large-scale manufacturers with their own evolving requirements.

    Trusted Supply: Lessons Learned as a Manufacturer

    Buyers and users often recognize the difference that comes from deep, hands-on production experience as opposed to simply trading or reselling. Years of facing production bottlenecks, surprise impurity peaks, and urgent regulatory audits taught us to focus on transparency and traceability. Every product, 2-Chloro-5-Trifluoromethylbenzyl Chloride included, reflects everything that went right—or wrong—back at the plant.

    We share real assay data, including non-spec extras on trace impurities, after pressure from customers who needed better reassurance for sensitive downstream processes. This shift took time but made it possible for more rigorous partners to rely on our output for GMP and ISO-validated runs. Failures became faster to address once full transparency took hold, with mutual trust built around open communication and consistent data sharing. Understanding precisely where the product came from, what went in, and how it was handled gives end users leverage and confidence.

    Trust in chemical supply comes from a proven record of responsiveness, hard-won improvements, and willingness to address even the inconvenient truths about manufacturing. Our commitment to this approach ensures that every container of 2-Chloro-5-Trifluoromethylbenzyl Chloride arriving at your facility reflects careful preparation, tested performance, and a sensitivity to your real-world requirements.

    The Manufacturer’s Perspective: Quality Beyond the Label

    Having produced and managed this product line for years, we know documentation alone does not replace day-to-day vigilance and direct measurement. We see our effort reflected through reproducibility in the field—the fewer surprises, the better. Successful partnership and product performance grow from shared standards and honesty about what works, what breaks, and how steady incremental improvements deliver lasting value for our customers.

    Every batch of 2-Chloro-5-Trifluoromethylbenzyl Chloride represents a long chain of decisions, lessons, and shared technical insight. By keeping the focus on practical quality and full traceability, we enable chemists, researchers, and industrial users to work faster, safer, and with results they can trust.