Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Pentafluorobenzyl Chloride

    • Product Name Pentafluorobenzyl Chloride
    • Alias PFB-Cl
    • Einecs 206-936-2
    • 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

    269276

    Product Name Pentafluorobenzyl Chloride
    Cas Number 320-84-1
    Molecular Formula C7H2ClF5
    Molecular Weight 218.54 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 143-145 °C
    Melting Point -31 °C
    Density 1.47 g/mL at 25 °C
    Refractive Index n20/D 1.476
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Flash Point 57 °C (closed cup)
    Odor Pungent
    Storage Temperature Store at 2-8 °C
    Synonyms PFB-Cl, α,α,α,2,3,4,5,6-Hexafluorotoluene-4-chloride

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

    Packing & Storage
    Packing Pentafluorobenzyl Chloride is supplied in a 25g amber glass bottle with a secure screw cap and warning hazard labels.
    Shipping Pentafluorobenzyl Chloride should be shipped in tightly sealed containers, away from heat, moisture, and incompatible substances. It is classified as a hazardous material and must comply with all relevant transportation regulations, including proper labeling and documentation. Typically, it is transported in secondary containment to prevent leaks during transit.
    Storage Pentafluorobenzyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, sunlight, and incompatible substances like strong bases or oxidizers. Use corrosion-resistant containers and keep away from sources of ignition. Store under an inert atmosphere, such as nitrogen, to prevent hydrolysis and degradation. Always clearly label the storage container.
    Application of Pentafluorobenzyl Chloride

    Applications of Pentafluorobenzyl Chloride in Industrial Manufacturing

    Pentafluorobenzyl Chloride is an advanced halogenated aromatic compound with high reactivity, supporting core synthesis steps in fine chemical, pharmaceutical, analytical, and agrochemical industries. As a direct manufacturer, we enable precise tailoring for downstream formulation and process control. Below, we detail specific industrial applications, key compliance needs, processing methods, and resulting product types seen in the market.

    1. Pharmaceutical Intermediates: Synthesis of Active Ingredients and Building Blocks

    This raw material plays a strategic role as a derivatization and alkylation agent in pharmaceutical synthesis. Manufacturers frequently rely on it for introducing pentafluorobenzyl groups during the preparation of advanced intermediates, APIs, and pharmacologically active heterocycles. Its use is particularly important for increasing molecular stability and enhancing bioavailability, often for cardiovascular, antiviral, and CNS agent classes. All downstream synthesis must meet stringent standards on trace impurities and residual solvent levels.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • USP/NF & Ph. Eur. for relevant API and intermediate monographs
    • 21 CFR Part 211 (FDA cGMP regulations for finished pharmaceuticals)
    • Chinese Pharmacopoeia quality and safety limits for process chemicals

    Typical usage ratio

    • 0.5–1.5 molar equivalent in alkylation steps; exact proportion depends on desired reaction selectivity, scale, and substrate sensitivity

    Downstream process integration

    • Introduced in early-to-intermediate synthetic stages, typically as an electrophile to attach the pentafluorobenzyl moiety to core or side-chain structures; followed by controlled hydrolysis, purification, crystallization, and rigorous analytical verification of residuals

    Final product types

    • Cardiovascular APIs bearing pentafluorobenzyl substituents
    • Antiviral and CNS-active drug intermediates
    • Fluorinated building blocks for combinatorial libraries
    • Patent-protected new chemical entities based on pentafluorobenzyl frameworks

    2. Agrochemical Synthesis: Pesticide and Herbicide Precursor Production

    Agrochemical manufacturers use this material for introducing pentafluorobenzyl functional groups in the synthesis of modern insecticide and herbicide actives. Such modifications can improve target selectivity, increase metabolic stability, and reduce application rates. Downstream formulation facilities require close control of process impurities, and all operators must meet specific agrochemical regulatory approvals prior to market launch.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 for production process documentation and traceability
    • EU Regulation (EC) No. 1107/2009 for pesticide approval
    • U.S. EPA guidelines for inert ingredient and intermediate assessment

    Typical usage ratio

    • 1.0–2.0 equivalents per target molecule based on active site requirements; batch scale adjusted according to downstream reactivity and purity needs

    Downstream process integration

    • Used in the primary reaction stage for coupling or alkylation with nitrogen, oxygen, or sulfur nucleophiles; followed by multi-stage purification, intermediate storage, and formulation blending for finished crop protection agents

    Final product types

    • Pentafluorobenzyl-substituted insecticides
    • Herbicide intermediates for grain, cotton, and soy treatment
    • Active ingredient concentrates for commercial agrochemical production
    • Custom compounds for regulatory screening and export markets

    3. Analytical Reagents: Derivatization of Polar Analytes for Chromatography

    In laboratory and industrial analytical chemistry, this material is a key derivatizing agent for transforming otherwise difficult-to-detect carboxylic acids, alcohols, phenols, and amines. Laboratories and contract testing centers select it to improve compound volatility and detection sensitivity in GC, GC-MS, and related techniques. The process demands highly pure input material and strict adherence to analytical method validation standards for compliance in regulated environments.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory competence
    • AOAC Official Methods for food and environmental testing
    • FDA guidelines for residue analysis and food safety labs
    • EN 15662 multiresidue pesticide analysis (GC-MS/LC-MS protocols)

    Typical usage ratio

    • Reagent-to-analyte ratio typically 1.2–2.0 equivalents, adjusted for sample matrix and target analyte concentration; minimum reagent excess is used to maximize conversion efficiency

    Downstream process integration

    • Added directly to sample extracts prior to chromatographic analysis, often with base or phase transfer catalyst; followed by solvent extraction, evaporation, and injection for quantification

    Final product types

    • Certified analytical reagents and standards
    • GC and GC-MS sample derivatives for food, environment, and pharmaceutical monitoring
    • Multi-residue screening kits and laboratory consumables
    • Custom derivatization kits for clinical or forensic laboratories

    4. Fine Chemical Manufacturing: Specialty Monomer and Ligand Synthesis

    Chemical synthesis plants utilize this material for the preparation of pentafluorobenzyl-functionalized monomers and specialty ligands. Its reactivity profile supports downstream processes in polymer science, catalysis, and dye manufacture. Production involves reaction step design for high substitution efficiency and targeted purification to meet narrow spectral and functional requirements in the end-use application.

    Industry compliance standards

    • ISO 9001/2015-certified quality management systems
    • REACH registration for chemical handling and downstream use
    • Local occupational health and safety regulations (GB 12268, OSHA 1910)
    • Customer-specific technical and purity specifications (NMR, GC-MS, HPLC)

    Typical usage ratio

    • 0.8–1.3 equivalents in nucleophilic aromatic substitution or alkylation reactions; loading varies by chemical structure and degree of functionalization required

    Downstream process integration

    • Fed into continuous-flow or batch reactors for coupling with aromatic cores or chelating ligands; followed by workup steps (phase separation, crystallization, drying) and advanced purification (recrystallization, column chromatography) to reach functional-grade output

    Final product types

    • Pentafluorobenzyl-functionalized polymers (film, coating, sensor applications)
    • Ligands and chelators for homogeneous catalysis
    • Special effect dyes and optical brighteners
    • Functional intermediates for electronics and specialty adhesives

    5. Environmental Monitoring: Reference Material Preparation

    Certified reference material producers and environmental testing labs employ this material for the synthesis of labeled reference standards and internal calibrants. These compounds ensure accurate quantification of trace pesticides and chlorinated pollutants in soil, water, and agricultural samples. Traceability, purity, and lot consistency must conform to accreditation criteria and international comparison standards.

    Industry compliance standards

    • ISO 17034:2016 for production of reference materials
    • ISO Guide 35 for reference material characterization
    • EN 17025 for analytical laboratory quality systems
    • EPA Method 8081/8141 for organochlorine pesticide analysis

    Typical usage ratio

    • Exact molar ratios depend on target analyte and desired isotope labeling; typically 1.0–1.1 equivalents used to ensure full functionalization without side reaction contamination

    Downstream process integration

    • Utilized in the key alkylation or derivatization step during reference compound synthesis; followed by rigorous purification, calibration against NIST or equivalent standards, and detailed certification documentation for external distribution

    Final product types

    • Certified reference standards (CRM/ERM) for regulatory labs
    • Isotope-labeled internal calibrants for chromatography
    • Proficiency testing kits for environmental pollutants
    • Analytical controls for routine environmental and residue labs
    Free Quote

    Competitive Pentafluorobenzyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Pentafluorobenzyl Chloride: Precision Chemical for Advanced Applications

    Our Experience in Manufacturing Pentafluorobenzyl Chloride

    Pentafluorobenzyl chloride marks a reliable building block for many demanding chemical syntheses. Years of development in our own facilities have given us a clear understanding of its necessary purity and behavior under real industrial conditions. We’ve worked alongside pharmaceutical, agrochemical, and analytical labs, observing where quality makes the final difference in application success. Our hands-on knowledge covers its challenges, from exacting purification needs to long-term product stability. Those years have also taught us which details—water content, trace contaminants, and packaging atmosphere—affect actual reaction yields for our end users.

    The model we produce is based on a purity grade exceeding the technical threshold most commercial suppliers offer. We’ve configured the process to achieve fewer byproducts and lower moisture content than many alternatives on the market. Our typical batch provides a clear, colorless to pale yellow liquid—characteristic for the compound at this purity grade—meeting the needs of both research-scale and tonnage-scale customers. Each lot ties back to a robust set of analytical controls developed through decades of iterative improvement and real-world troubleshooting.

    Chemical Profile and Industry Usage

    Pentafluorobenzyl chloride finds its main value as a reactive alkylating agent. Our customers rely on it to introduce the pentafluorobenzyl group into a range of molecular scaffolds. Over time, we’ve seen its core applications settle into three areas: pharmaceutical intermediate synthesis, environmental analysis, and custom molecule design. In our experience, environmental labs often demand exceptional batch-to-batch consistency, as the compound serves as a reliable derivatization reagent in GC analysis of pesticides, phenols, and carboxylic acids. Even small variations in byproduct content can skew results at these sensitivity levels, underlining the importance of rigorous quality systems.

    The pharmaceutical sector uses pentafluorobenzyl chloride mainly for introducing stability features into bioactive candidates. Its strong electron-withdrawing effect, born from the pentafluoro arrangement, enables unique reactivity. We’ve tracked shift in usage patterns: earlier, most demand came from specialty research firms. Recent advances in fluorinated drug design have brought bulk orders from commercial process facilities, which brings its own logistical and quality control considerations. Some syntheses require anhydrous deliveries, and we now offer tailored packaging under inert gas to prevent degradation before use.

    Some specialty use cases see pentafluorobenzyl chloride as a tool in fine chemical manufacturing and advanced materials, for instance as a precursor in liquid crystals or as part of non-standard polymer synthesis. Over many years, we’ve seen end users experiment with less pure alternatives, and outcomes consistently tracked back to contamination—halide impurities or incomplete fluorination waste hours of skilled labor downstream.

    What Makes Pentafluorobenzyl Chloride Distinct

    Many buyers initially confuse pentafluorobenzyl chloride with simple benzyl chloride or with trifluoromethyl-substituted analogues. Chemically and in process, these compounds respond quite differently. Five fluorines on the aromatic ring increase the compound’s electrophilicity far above monochlorinated or difluorinated relatives. The C–Cl bond becomes more reactive, especially in nucleophilic substitution; this property underpins its popularity in advanced organic synthesis. Through our day-to-day work with these materials, we’ve found no real substitute for pentafluorobenzyl chloride where high-yield, clean alkylation is needed in fluorinated frameworks. Trifluoromethylbenzyl chloride, while structurally related, offers noticeably lower yields and leaves more byproducts in critical reactions.

    Handling, storage, and shipping of pentafluorobenzyl chloride draw special attention at our facility, much more than simple benzyl chloride. The reactivity that makes it effective as a derivatizing agent also means water and light exposure quickly degrade its quality. Our setup features sealed glass and PTFE lines, rigorous nitrogen purging, and humidity-controlled rooms. Each bottle is filled and capped under inert atmosphere. We developed these protocols after seeing how oxygen and water contact even at low ppm levels led to side reactions, discoloration, and off-odors in batches from less controlled environments.

    Why Pentafluorobenzyl Chloride Matters for Advanced Synthesis

    Efficient syntheses often demand intermediates that react promptly and predictably, leaving few side products. Pentafluorobenzyl chloride’s particular structure supports these aims: the heavily fluorinated ring draws electron density so powerfully that, in practice, most nucleophilic partners—thiols, alcohols, amines—will react fully at lower temperature and with fewer hazardous byproducts. Our production team directly observed that using lower-purity or moisture-contaminated pentafluorobenzyl chloride leads to incomplete reactions and the need for expensive, time-consuming purifications. These insights have informed not only our own process optimization but also many trouble-shooting conversations with our client labs.

    Demand for pentafluorinated intermediates has only grown with the expansion of modern medicinal chemistry. Incorporating fluorine atoms can improve metabolic stability, bioavailability, and binding affinity in potential drug molecules. Pentafluorobenzyl chloride often acts as the final, precise touch on a complex molecule, where any variation in purity may throw off an entire development process. Over years of fielding technical questions and supporting validations, our team built custom solutions: stabilized packaging, technical certificates covering minor impurity profiles, and rapid analytics as feedback loops for client R&D teams.

    Differences Compared to Other Halogenated Benzyl Compounds

    Our years working on the plant floor and in QC labs have shown, more than any technical literature can convey, how pentafluorobenzyl chloride behaves uniquely versus its nearest neighbors. In bench reactions, simple benzyl chloride’s aromatic ring contributes minimal electron withdrawal, making its C–Cl bond less reactive and often necessitating harsher, less selective conditions. Trifluorobenzyl chloride, carrying fewer fluorines, does not reach the same activity. We’ve seen synthetic chemists seeking to economize with cheaper analogs routinely run into lower yields, more side product formation, or total failure in critical coupling steps meant for pentafluorobenzyl chloride.

    Cost and handling requirements differ as well. More reactive, high-purity pentafluorobenzyl chloride justifies specialized storage and transport investment. A drum of benzyl chloride can ship with basic precautions, but our pentafluorinated product goes out under multi-layer seal, often cooled, with humidity and oxygen prevented throughout the chain. These layers of protection are not just bureaucratic hurdles; they reflect real-world experience—product arriving with trace hydrolysis, or premature degradation, creates waste and undermines both cost and scientific progress in partners’ operations.

    Specification Evolution and Process Improvements

    Sourcing high-quality pentafluorobenzyl chloride on a global scale introduced us to variable market standards. We faced a steep learning curve matching documentation from upstream materials with genuine end-use results. Over the years, we’ve pressed our entire supply network, from fluoride feedstocks to purification solvents, toward tighter controls. Today, our specification consistently targets impurity levels below 0.5 percent for major contaminants, and we maintain moisture below 0.05 percent by the time it ships. These benchmarks arose not from abstract industry standards, but from direct feedback when clients identified problematic side reactions or color changes from other suppliers’ looser specifications.

    Our batch records link every step, from raw material intake—periodically re-verified using NMR, GC-MS, and KF titration—through to finished goods. Packaged samples go through accelerated stability checks. This vigilance was born out of necessity. Earlier in our history, less rigorous inspection allowed minor variances between shipments, and client results varied in turn. These days, our team traces every out-of-spec lot to its exact process step, closing the gap between cradle and final delivery. Quality shifts imposed by changes in raw material sources, temperature fluctuations, or cleaning protocols now show up in real time via in-process controls.

    Supporting Analytical and Synthetic Work in Application

    Many environmental labs depend on pentafluorobenzyl chloride for derivatizing chemical pollutants before detection. Pesticide, phenol, and acid analysis in complex samples rests not just on the instrument, but on the reliability of the derivatization agent. Our experience confirms that batch inconsistency in moisture, residual reactants, or trace halides will degrade chromatographic results, giving unreliable baselines or ghost peaks. To help our partners, we maintain a sample retention program, archiving each lot for years. When an issue does arise, we rapidly reproduce small-scale derivatizations in our internal labs to replicate and diagnose problems—in many cases the root cause traces back not to the end-user handling, but to inconsistent production by suppliers with less rigorous controls.

    Industrial and pharmaceutical R&D teams rely on pentafluorobenzyl chloride to modify molecules for specific reactivity or solubility profiles. Some routes require the addition of precisely this group, with no tolerance for even minor contamination by isomeric or incomplete fluorination. Accurate reaction scale-up begins with certainty about reagent purity. In our history, unexpected byproducts—arising from trace monochloro or difluoro compounds—created significant headaches even at PPB levels, generating hard-to-remove colored or insoluble residues. To mitigate this risk, we employ a series of packed-column chromatographic and distillation steps tailored to this product. Even experienced chemists often overlook the impact of this process detail until working on kilogram or ton batches, where even minute process errors multiply.

    Responding to Industry Trends and Technical Challenges

    Greater regulatory scrutiny around residual byproducts and solvent residues puts pressure on chemical manufacturers to continuously enhance purification and detection capabilities. We invest in analytical instrumentation that not only supports release testing, but also supports rapid troubleshooting and process optimization. Mass spectrometry and advanced chromatography give us confidence each batch falls within tighter bounds than those set by historical commodity standards. Our analytic scientists run routine stability checks, modeling field conditions based on end-user survey feedback. Over the past five years, we’ve responded to more regulatory questions about trace solvents than the previous decade. This shift requires real-time adaptation, as new compliance and safety standards affect allowable impurity levels across global markets.

    The push for greener chemistry also affects pentafluorobenzyl chloride demand. Customers experiment with alternative solvents, milder reaction conditions, and renewable feedstocks. We engage with partners and thought leaders to adjust our process to reduce waste, improve yield, and minimize potential environmental releases. Modifying synthesis routes and distillation steps aids product quality and environmental compliance in equal measure. These changes are not abstract goals but ongoing projects driven by direct customer feedback and evolving regulations in key markets.

    Supporting Customers with More than Product Alone

    Chemical manufacturing is as much about partnership as it is about process. Scientists and technicians at our company regularly consult with clients to interpret analytical results, troubleshoot synthetic failures, and recommend best practices for safe handling and usage. Our technical service team is staffed by chemists who understand the nuances and lived reality of working with pentafluorinated reagents. We have prepared custom documentation, supported on-site audits, and shared anonymized lessons learned from field issues, all so the next batch reaches the user in optimal form and with clear, transparent data.

    We know procurement teams value predictability, so our logistics personnel optimize shipping and delivery based on seasonal and geographic factors. Extreme temperatures and customs delays learned from years of international shipping prompt us to maintain specialized storage, packaging, and tracking routines. If a question arises about expired material, cold-chain disruption, or batch identification, our records and expertise support clear resolution.

    We also recognize the importance of continual improvement, both in process and support. Feedback from customers—failures, successes, and all points in between—drives our process development. Each close call, near miss, or successful scale-up becomes a case study that shapes the training and protocols for our next generation of operators and technical support staff.

    Meeting Future Challenges with a Foundation in Experience

    The future for pentafluorobenzyl chloride lies as much in innovation as in reliability. Emerging applications in specialty materials, biomolecule labeling, and precision diagnostics will demand even higher accuracy and tailored delivery options. Our company positions itself at the front of these trends by continuing to refine process controls, improve analytical benchmarks, and support client innovation through open dialogue. Those improvements rest on a foundation set by decades of practical experience. We have seen first-hand how even small process or analytical adjustments support breakthroughs in the pharmaceutical, life science, and analytical sectors. That experience translates into greater value for partners seeking performance and peace of mind from every shipment.

    We continue to learn, adapt, and share our knowledge both within the company and with the broader community of chemists and engineers. Pentafluorobenzyl chloride is not just another commodity; it demands commitment to detail, technical rigor, and a collaborative spirit from manufacturer to end user. Every drum and bottle carries forward the lessons and care of those who have worked directly with its demanding reactivity, unique properties, and transformative potential.