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2,3,5,6-Tetrafluorophenylhydrazine

    • Product Name 2,3,5,6-Tetrafluorophenylhydrazine
    • Alias TFPH
    • Einecs 407-410-1
    • 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

    184730

    Productname 2,3,5,6-Tetrafluorophenylhydrazine
    Molecularformula C6H4F4N2
    Molecularweight 180.10
    Casnumber 2947-69-9
    Appearance Solid, usually off-white to light yellow
    Meltingpoint 89-92°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥97%
    Storageconditions Store at 2-8°C, protected from light and moisture
    Synonyms TFPH; Tetrafuorophenylhydrazine
    Smiles NNc1c(F)cc(F)cc1F
    Hazardclass Harmful if swallowed, causes skin irritation

    As an accredited 2,3,5,6-Tetrafluorophenylhydrazine 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, tightly sealed, labeled with chemical name, hazard symbols, and handling instructions for 2,3,5,6-Tetrafluorophenylhydrazine.
    Shipping 2,3,5,6-Tetrafluorophenylhydrazine should be shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical, requiring packaging compliant with international transport regulations. Appropriate labeling and documentation are mandatory. Handle and transport with caution, ensuring all safety protocols are followed to prevent exposure or contamination.
    Storage 2,3,5,6-Tetrafluorophenylhydrazine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials such as oxidizing agents and acids. Use appropriate, chemically resistant containers and ensure proper labeling to prevent accidental misuse or contamination.
    Application of 2,3,5,6-Tetrafluorophenylhydrazine

    Applications of 2,3,5,6-Tetrafluorophenylhydrazine in Industrial Manufacturing

    2,3,5,6-Tetrafluorophenylhydrazine acts as an advanced organic synthesis intermediate, finding core applications across specialized chemical manufacturing sectors where fluorinated hydrazine derivatives enable high-value transformations. All listed scenarios are based on established uses in fine chemicals, crop protection, advanced polymer synthesis, and pharmaceutical R&D. Our expert manufacturing team supports strict quality controls and regulatory traceability throughout downstream integration.

    1. Synthesis of Fluorinated Pyrazole Crop Protection Agents

    Leading agrochemical manufacturers utilize this material as a reactive nucleophile to construct pyrazole rings featuring multi-fluorine substitution, which are critical scaffolds in many modern insecticide and herbicide active ingredients. By enabling direct hydrazinolysis with advanced diketone substrates, this building block affords high product purity and consistent batch yields under controlled temperature and solvent systems.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006, Annex XVII – for raw material sourcing and pre-registration
    • ISO 9001:2015 and ISO 14001:2015– site-level quality and environmental systems for crop protection active ingredient production
    • OECD GLP Guidelines for agrochemical intermediate processing
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) – for finished AI registration

    Typical usage ratio

    • Batch reactions typically employ 1.05–1.10 molar equivalents relative to diketone reactants to ensure full ring closure and minimize excess handling during pyrazole core formation. Adjustments are made based on scale and the electronic nature of the co-reactant.

    Downstream process integration

    • This hydrazine derivative enters the process during the heterocycle-forming step, often after pre-functionalization of fluorinated diketones. The subsequent hydrazinolysis and cyclization occur in aprotic solvents at 20–40°C, with on-line monitoring for endpoint determination. Purification typically involves crystallization or column chromatography prior to downstream derivatization or formulation into AIs.

    Final product types

    • Pesticide active ingredients (AIs) for pyrazole-based herbicides and insecticides
    • Technical-grade crop protection intermediates
    • Formulated agrochemical products (liquid, granular, and wettable powder formulations)
    • AI blends for pre-mix or post-mix pesticide manufacturing

    2. Active Intermediate in Pharmaceutical Research and Development (R&D)

    Medicinal chemistry teams in pharmaceutical R&D select this compound for multi-step syntheses of bioactive heterocycles, particularly for generating fluorinated pyrazoles, triazoles, and related molecules with improved metabolic stability. The compound’s controlled reactivity and electron-deficient phenyl ring facilitate regioselective transformations crucial in lead optimization campaigns and early-stage drug substance synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (APIs)
    • USP–NF requirements for raw material testing (where applicable for intermediates)
    • FDA 21 CFR Part 211 (for pilot and production scale under cGMP)
    • EMA Guidelines on the Sterilization of Medicinal Products (for intermediates used in parenteral routes)

    Typical usage ratio

    • Typical batch molar ratios range from 1.00–1.20 equivalents, based on the type of coupling or cyclization step. In medicinal chemistry screening, excess hydrazine is sometimes used for incomplete or poorly reactive substrates, with recovery steps implemented in scale-up.

    Downstream process integration

    • The raw material is added during ring-closure chemistry, often following acylation or halogenation of the core aromatic system. Integration typically occurs in multi-step batch reactors, with in-process controls for purity and excess reagent removal before subsequent derivatization or isolation of target heterocycles.

    Final product types

    • Pharmaceutical research intermediates (fluorinated heterocycles, especially pyrazoles and triazoles)
    • Reference standards for analytical testing
    • Screening libraries for drug discovery
    • Preclinical drug candidates containing fluorinated aryl hydrazine linkages

    3. Precursor for Fluorinated Specialty Polymer Monomers

    Polymer manufacturers employ this hydrazine derivative as a key monomer precursor to introduce multiple fluorine functionalities and hydrazine-derived subunits into specialty polymer chains. Such modifications enhance chemical durability, hydrophobicity, and dielectric properties required in functional coatings, electronics encapsulants, and membrane materials for advanced engineering applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer production
    • RoHS Directive (EU) 2011/65/EU – for electronics-graded materials
    • UL 94 Flammability Standard (for final polymer use)
    • IEC 60695 Electrical Insulating Properties (for relevant applications)

    Typical usage ratio

    • Formulations typically dose the precursor at 0.5–5 mole percent in copolymer feedstocks, depending on the targeted proportion of hydrazine/fluorine substitution. Ratios adjust for required chemical resistance, hydrophobicity, or dielectric performance in specific finished polymer types.

    Downstream process integration

    • The material is introduced during monomer synthesis or polymerization, through solution phase or melt polymerization techniques. Hydrazine-containing intermediates react with fluorinated acid chlorides or isocyanates, followed by copolymerization with acrylates, vinyl ethers, or other comonomers to yield functionalized polymer backbones.

    Final product types

    • Fluorinated specialty polymers for anti-corrosive coatings
    • High-performance dielectric films for electronics and sensors
    • Membrane and separation materials with tailored wetting properties
    • Fluorinated copolymers for advanced adhesives and sealants

    4. Functionalization Agent for Analytical Labeling Reagents

    Producers of analytical chemistry reagent kits incorporate this compound for the synthesis of fluorinated phenylhydrazine-based derivatization agents, which serve as selective labeling reagents in HPLC, GC-MS, and bio-analytical protocols. The electron-withdrawing nature of these groups enhances detection sensitivity and allows for specific derivatization of carbonyl-containing analytes, vital for clinical diagnostics and complex sample analysis.

    Industry compliance standards

    • ISO/IEC 17025 Accreditation Requirements for testing laboratories
    • FDA 21 CFR Part 820 (for manufacturers of clinical diagnostic devices)
    • CLSI (Clinical and Laboratory Standards Institute) guidelines for reagent validation
    • USP monographs for analytical reagent quality (where applicable)

    Typical usage ratio

    • Hydrazine derivatives are formulated in labeling kits at 0.2–2 weight percent, adjusted for the targeted substrate concentration and analytical detection limits. Optimization occurs during kit development for minimal background and high labeling efficiency.

    Downstream process integration

    • Our product is used during the functionalization of silica or polymer supports, or in the direct synthesis of small molecule derivatization agents. The material enters during diazotization or coupling reactions, prior to purification and blending with compatible buffers or solvents to ensure reagent stability and shelf-life.

    Final product types

    • HPLC and GC labeling kits for clinical and food safety analysis
    • Fluorescent derivatization reagents for protein and peptide quantification
    • Specialty kits for carbonyl group determination
    • Surface-functionalized analytical beads and columns
    Free Quote

    Competitive 2,3,5,6-Tetrafluorophenylhydrazine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 2,3,5,6-Tetrafluorophenylhydrazine: Crafted for Reliable R&D Progress

    Our Perspective from the Production Floor

    We’ve been producing specialty fluorinated chemicals for over a decade, and over time, certain products have proven themselves not just popular, but genuinely essential for innovation. 2,3,5,6-Tetrafluorophenylhydrazine stands among those rare materials that researchers and process chemists continue to request, project after project, for their needs in the field of advanced intermediates and pharmaceutical building blocks. The product owes its reputation to the way it fits seamlessly into organic synthesis strategies, especially when the introduction of specific fluorine patterns makes or breaks the function of a target molecule.

    What Sets 2,3,5,6-Tetrafluorophenylhydrazine Apart?

    In our experience working directly with chemists, the main draw of 2,3,5,6-Tetrafluorophenylhydrazine comes down to selectivity and the unique reactivity it brings. Not every hydrazine is cut from the same cloth — and we’ve seen a tendency in some labs to treat all phenylhydrazines as interchangeable. The distinct arrangement of four fluorine atoms at the 2,3,5,6-positions creates profound changes in electron density, yielding effects that stretch beyond the usual hydrazine coupling or reduction roles.

    Those fluorine atoms aren’t just cosmetic changes. They transform reactivity, influencing nucleophilicity and the ease of downstream derivatization. Cyclization reactions proceed under milder conditions, and the presence of electron-withdrawing fluorines minimizes the risk of byproducts that often dog other phenylhydrazines. Based on route scouting and method development projects we’ve supported, the C6H2F4NHNH2 motif reduces tedium for the bench chemist because it minimizes reagent tuning from batch to batch.

    Specifications and Consistency in Supply

    On the manufacturing side, purity defines the product’s value, and impurities create research headaches. Our batches of 2,3,5,6-Tetrafluorophenylhydrazine routinely surpass a GC purity of 98%. We validate every lot by NMR and confirm the structure through IR and LC-MS, as nothing undermines a synthesis more thoroughly than a hidden contaminant. Bulk and research-scale requests both pass through the same QA process; research chemists deserve to start from a worry-free base, whether they're ordering grams or kilograms.

    Long-term clients value the fact that our synthesis process excludes the use of heavy metals at any step, which removes one headache for those with a focus on downstream medicinal chemistry or environmental stewardship. If you have a complicated reaction sequence, knowing you are not introducing any transition metal is comforting. We've maintained batch-to-batch color consistency, typically ranging from pale yellow to off-white, which has helped certain clients spot degradation or mishandling at a glance.

    Key Applications: What We See in the Field

    Most requests for this molecule come from R&D teams exploring new fluorinated heterocycles, especially triazoles and pyrazoles. Our direct conversations with leading pharmaceutical companies suggest that hydrazines like this play a pivotal role in the formation of advanced intermediates for oncology and CNS pipeline compounds. The distinct substitution pattern ensures higher yields in diazotization and cyclocondensation reactions, particularly when compared to mono- or difluorinated analogues.

    Academic researchers working on small-molecule libraries for screening panel development also tend to favor this hydrazine, as the 2,3,5,6-tetrafluoro group creates favorable physicochemical properties—such as increased metabolic stability and altered lipophilicity—without heavily increasing the molecular weight. An added layer of utility arrives whenever certain sensitive tetrazole or triazine motifs are under study; our product’s specific substitution pattern has slowed decomposition and side-reactions versus less-fluorinated relatives.

    Why Not Just Use Other Phenylhydrazines?

    This question comes up again and again, especially from process chemists trying to keep costs low or source material from existing stocks. In-house, we directly compare 2,3,5,6-tetrafluorophenylhydrazine with more conventional hydrazines, fluorinated or not, in new project route explorations. The four fluorines give a balance of reactivity without the excessive electron deficiency you see in pentafluorophenylhydrazine, which can be prone to poor yields or complex purification steps. If someone expects a direct swap between the di- and tetrafluorinated versions, subtle differences show themselves quickly: lower melting points, different solubility profiles, and shifts in optimal solvent choices.

    Additionally, purity challenges with other hydrazines arise from less stable isomers and dark-colored impurities. Our feedback loops with scale-up teams revealed, for instance, that the 3,4,5,6-tetrafluoro isomer often brings solubility issues and can undergo unsought side reactions under mild acidic conditions. Our product minimizes those headaches.

    Handling and Storage: Practical Lessons Learned

    Our packaging contains the hydrazine in light-blocking, sealed glass bottles. Over the years, we've learned—often through customer reports—that exposure to air and light can degrade both appearance and performance, especially over many weeks. We move fast on customer requests for documentation, but real-world stability always beats paperwork. Those storing open containers for more than a month will see a shift in color and, sometimes, a less reliable performance in critical couplings. That isn’t unique to our product; it’s a feature of the chemical class. Good practice is to prepare fresh solutions and keep the material sealed cool and dry, but we worked to ensure our batches meet stability benchmarks under typical lab lighting for at least six months.

    For bulk consumers, kilo-quantities are sealed under nitrogen whenever feasible, and we use robust transport containers. No matter how good the product is at leaving our production line, careless courier handling or customs delay can turn top-notch hydrazine into a shelf curiosity. We keep direct communication lines open for bulk buyers, so handling issues get resolved before they impact research timelines.

    Environmental and Safety Point of View

    Making and supplying hydrazines means we think daily about health and safety. There is nothing theoretical about this—anyone who’s spent time in small-molecule synthesis knows hydrazines require respect. We train our staff, invest in local exhaust and scrubbing, and share data openly on safe handling for every customer. Hydrazine derivatives, especially those heavily substituted with fluorines, can bring unique hazards, so we committed early to providing realistic handling advice based on real-world lab reports, not just literature values.

    Waste management is another layer: our production avoids unnecessary side products and solvents that complicate waste disposal, since these are all costs for downstream users. Regular audits and customer feedback told us that small variations in impurity profiles matter—not just for purity, but for avoiding nasty surprises in waste-processing steps. We always welcome new suggestions from experienced synthetic chemists on improving batch reproducibility or minimizing end-of-life concerns. Sharing this feedback back to our process engineers tightens the loop between production and point-of-use.

    Lessons from Process Chemistry & Route Development

    We maintain site visits and open communication with both pharma and academic partners. In process chemistry, scalability reveals strengths and weaknesses fast. 2,3,5,6-Tetrafluorophenylhydrazine showed resilience in multi-step routes, with reduced formation of troublesome impurities. In some scale-ups, our clients were able to run their key reactions at slightly higher temperatures or lower catalyst loadings, thanks to the predictable reactivity profile. In one case, a partner moved from pilot to commercial production of a fluorinated triazole intermediate with fewer filtration steps, purely because cleaner input hydrazine speeds up work-up and reduces solvent volume.

    Another lesson: documentation and service don’t mean much if supply chains fail during late-stage development. During the early pandemic period, our factory adopted dual-source raw material procurement and brought analytical services in-house. Keeping supply steady and transparent, instead of chasing spot-buys, meant that even during logistics crunches, our clients finished projects on time. Our take is simple: robust sourcing and transparent manufacturing practices let research teams focus on discovery, not paperwork or uncertainty.

    Supporting Novel Discovery in Medicinal Chemistry

    Many research teams building out new lead series need reagents with established data and consistent analytical support, without cutting corners on safety or performance. Over the past several years, our involvement in collaborative projects—whether through direct supply contracts or joint method development—has shown that 2,3,5,6-tetrafluorophenylhydrazine can open up new motifs inaccessible with older hydrazine choices. We keep our doors open for feedback: informal tech calls, samples, or rush shipments. And if a user runs into issues—clogged lines, off-target byproducts, or unusual degradants—our production and analytical teams can help push through the bottleneck.

    As a manufacturer, we see the product as not only a chemical but as an enabler for trying out new transformations. Surveying published literature and speaking with investigators, the motif appears in a surprising range of high-value targets. Whether the user's focus is fluorinated agrochemicals, advanced dyes, or fragments for click chemistry, the role of this specific hydrazine emerges as a quiet workhorse. Good chemistry depends on more than what's written on the label.

    Supply Chain Values: Keeping Things Real

    Transaction costs and paperwork tend to bog down innovation. Our operation works to keep conversations simple: we discuss lead times, deliver to agreed specs, and don’t over-promise. We have worked through issues like customs delays and real-life shipping disruptions, which taught us that simple, direct service does more for client trust than a shelf full of certificates. A quick phone call or direct email can resolve most logistics hiccups— we encourage customers to reach out before minor issues grow into costly delays.

    For research orders, we’ve created small-batch, on-demand production runs, which let teams receive fresher material than what sits in central warehouses. For larger requests, our batch reservation system lets groups lock in supply for several months, reducing the scramble for key intermediates in busy periods. These practices stem from daily experience—stock-outs and "available in three weeks" responses can damage far more than a tight research schedule.

    The Margin of Difference: A Value Beyond the Molecule

    Since we sit on the manufacturing end, it’s crystal clear how a successful project often depends on material reliability as much as intellectual horsepower. Subtle purity changes or inconsistent physical properties create drag on progress, especially at scale. Our staff run parallel checks on physical appearance, NMR patterns, and thermal stability before listing any lot as ready. Over time, this attention to minor details limits batch-to-batch surprises. If a researcher needs to reproducibly establish a new SAR series or manufacture multi-gram quantities for in-vivo studies, the margin lies not just in purity, but predictability in how the material behaves in real-world protocols.

    Post-market support matters, too. We keep systematic records of any complaints or off-purity returns. These files inform small but ongoing improvements in process and packaging so even experienced users can rest assured their investment in a new route won’t be derailed by variable input quality. The trust we build up has not come about due to blanket guarantees or marketing promises, but slow, methodical improvements and honest dialogue.

    How We Keep Improving

    Continuous improvement guides our workflow. Routine audits, side-by-side comparisons with global competitors’ samples, and new test methods ensure that we aren’t just matching, but exceeding baseline expectations. We also maintain partnerships with university labs to evaluate new properties for the product, since feedback from experimental work tends to highlight real-world limitations and suggest future tweaks.

    Industry consortia and working groups have included our team in discussions on sustainable synthesis of fluorinated organics, where our staff contributed not just the product but hard data on energy use, solvent recovery, and lifecycle footprint. Our behind-the-scenes consulting with multinational drug innovators often leads to better target molecule platforms, as researchers trading technical notes with our analytical staff often find new uses or optimization windows.

    Final Thoughts

    The impacts of fluorinated building blocks extend far beyond their immediate applications. Since the introduction of 2,3,5,6-tetrafluorophenylhydrazine into our portfolio, we’ve observed clear progress in the tightrope walk of selectivity versus yield, purity versus ease-of-use, and supply versus cost. We hope that by sharing the manufacturing context and bottlenecks openly, we make it easier for chemists at the bench to see not just a compound, but a reliable partner for their next synthesis challenge.

    Most importantly, our product exists because research demands more than mediocrity—advanced chemistry requires advanced materials managed by those who understand the difference between the ordinary and the exceptional. Our doors are always open to new ideas, whether in product improvement, joint development, or troubleshooting complex routes. That’s the spirit that continues to shape the success stories our clients write, and the reason our team takes pride in every batch of 2,3,5,6-tetrafluorophenylhydrazine we send out into the world.