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1-(4-Fluorophenyl)Piperazine

    • Product Name 1-(4-Fluorophenyl)Piperazine
    • Alias p-FPP
    • Einecs 629-011-2
    • 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
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    Specifications

    HS Code

    905396

    Chemical Name 1-(4-Fluorophenyl)piperazine
    Cas Number 62041-95-6
    Molecular Formula C10H13FN2
    Molecular Weight 180.22 g/mol
    Appearance White to off-white solid
    Melting Point 56-58°C
    Boiling Point 262°C at 760 mmHg
    Solubility Soluble in water and organic solvents
    Density 1.14 g/cm3
    Purity Typically ≥98%
    Smiles C1CN(CCN1)C2=CC=C(C=C2)F
    Inchi InChI=1S/C10H13FN2/c11-9-3-1-8(2-4-9)13-6-5-12-7-13/h1-4,12H,5-7H2

    As an accredited 1-(4-Fluorophenyl)Piperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 100g amber glass bottle, the label reads "1-(4-Fluorophenyl)Piperazine," with hazard warnings and batch details.
    Shipping **Shipping Description for 1-(4-Fluorophenyl)Piperazine:** This chemical is shipped in tightly sealed containers, compliant with chemical safety regulations. Packaging includes appropriate hazard labeling and documentation. The item is dispatched via licensed carriers equipped to handle chemicals, ensuring safe transport under controlled temperature and conditions to prevent contamination, degradation, or unauthorized access.
    Storage 1-(4-Fluorophenyl)piperazine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. It must be kept away from incompatible substances such as strong oxidizing agents. Properly label the container and ensure access is limited to trained personnel. Avoid exposure to moisture and sources of ignition to maintain stability and safety.
    Application of 1-(4-Fluorophenyl)Piperazine

    Applications of 1-(4-Fluorophenyl)Piperazine in Industrial Manufacturing

    As an established producer of 1-(4-Fluorophenyl)Piperazine, we supply this specialty raw material to manufacturers serving various regulated sectors worldwide. The following application scenarios illustrate how downstream industries leverage its targeted reactivity for formulation, processing, and end-use product value in alignment with prevailing global compliance frameworks.

    1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Drug Synthesis

    Pharmaceutical manufacturers utilize 1-(4-Fluorophenyl)Piperazine as a building block in the multistep synthesis of certain central nervous system (CNS) drug molecules, particularly within the development of selective serotonin receptor modulators. Our material undergoes stringent quality control to support reproducible formation of key piperazine-linked scaffolds. Integration into stepwise batch synthesis occurs after halogenation and under protective atmosphere to maximize yield and target distinct N-aryl derivatives. As this intermediate is designed for regulated final APIs, its traceability and purity documentation form integral parts of the downstream regulatory submission package.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP) reference for intermediates
    • EU Chemicals Regulation (REACH) Annex VII-VIII
    • 21 CFR Parts 210/211 (US FDA drug manufacturing controls)

    Typical usage ratio

    • 0.18–0.32 molar equivalents per batch, adapted to molar balance in synthesis; ratio depends on route-specific coupling demands

    Downstream process integration

    • Used as a coupling agent in condensation or alkylation stage after initial raw material preparation
    • Introduced into jacketed reactors under inert atmosphere; monitored for conversion and impurity profile by HPLC/GC-MS controls
    • Followed by hydrolysis, protection/deprotection, or oxidative transformation steps depending on target API

    Final product types

    • N-aryl piperazine CNS drug intermediates
    • Finished CNS APIs (after further synthetic modification)
    • Research and reference standards supplied to global pharmaceutical laboratories

    2. Fine Chemical Building Block for Agrochemical Active Synthesis

    Crop protection manufacturers source this compound for use as a functionalized piperazine intermediate, supporting multi-stage synthesis of fluorinated agrochemical actives. It enters the process at an early condensation step, enhancing the activity and stability profile of the target molecules. Producers precisely control addition quantities, adhering to documented standard operating procedures to ensure consistent structural incorporation and facilitate downstream purification. Stability assessment follows batch integration, supporting regulatory submission for agrochemicals in diverse regulatory regions.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO/WHO Specifications for Pesticides
    • OECD Good Laboratory Practice (GLP) for agrochemical synthesis
    • EU Plant Protection Product Regulation (EC) No 1107/2009
    • China GB 4839-1997 (Quality Standard for Technical Pesticides)

    Typical usage ratio

    • 0.12–0.25 molar equivalents per synthetic cycle, refined according to active structure and reactivity of other halogenated intermediates

    Downstream process integration

    • Incorporated in the nucleophilic aromatic substitution and cyclization step following initial halide activation
    • Managed under reflux or controlled-temperature synthesis depending on downstream activity requirements
    • Intermediate isolated and purified prior to final step-up to finished pesticide or herbicide

    Final product types

    • Fluorinated fungicide and insecticide active compounds
    • Structural intermediates for novel herbicidal candidates
    • Agrochemical research samples for pre-registration field trials

    3. Key Intermediate in Specialty Dye and Pigment Manufacture

    Select dye and pigment manufacturers integrate this compound as a core diamine intermediate in the synthesis of functionalized organic colorants, primarily for high-performance textile and polymer applications. The reactive piperazine ring enables efficient coupling with activated aromatic systems, forming vivid and persistent molecular chromophores. Downstream addition occurs under closed vessel conditions with calibrated temperature controls, preventing side-products that could impact chromatic properties or dispersion stability in applied films or fibers.

    Industry compliance standards

    • Oeko-Tex Standard 100 (restricted substances for textile dyes)
    • EU REACH Annex XVII for aromatic amines
    • ISO 9001:2015 for pigment synthesis QC
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 3–7% by mole, referenced to target chromophore backbone size and intended application brightness depth

    Downstream process integration

    • Enters azo or anthraquinone coupling reactions as the diamine donor
    • Integrated under pH-controlled batch or continuous aqueous/organic phase process
    • Post-coupling filtration and standardization of dye concentration for delivery to downstream formulators

    Final product types

    • High-intensity textile disperse and acid dyes
    • Organic pigments for technical polymers
    • Specialty inks for plastics and synthetic fibers

    4. Intermediate for Polymer Modifier and Resin Additive Synthesis

    Technical polymer and specialty resin producers employ 1-(4-Fluorophenyl)Piperazine as a valuable intermediate for tailoring chain-modified resins. It supports the production of functional materials used in anti-corrosive coatings, advanced composites, and specialty adhesives. The material is loaded through metered feed into formulated polycondensation or step-growth polymerization systems. By adjusting the mole ratio, downstream engineers can precisely influence the molecular weight distribution and final performance properties, ensuring compatibility with application-specific durability and processability requirements.

    Industry compliance standards

    • ISO 14001 (environmental management in specialty chemical synthesis)
    • EU REACH registration (substance identity and use documentation)
    • RoHS Directive 2011/65/EU for polymer additives in electronics
    • ASTM D256 for Impact Resistance of Plastics

    Typical usage ratio

    • 0.8–2.3% by weight of total monomer input, adjusted according to desired function group density in the chain or network structure

    Downstream process integration

    • Added to pre-polymer mixture prior to catalyst introduction in step-growth resin synthesis
    • Incorporated under strictly controlled temperature ramps (140–180°C), with online monitoring of viscosity and conversion
    • Post-reaction standardization by vacuum distillation or solvent precipitation to achieve consistent application-grade material

    Final product types

    • Chain-modified epoxy or polyurethane resins
    • Functionalized polymer additives for anti-corrosion or adhesion boosting
    • Specialty resin-based coatings for automotive and marine use

    5. Research Chemical for Advanced Heterocycle Synthesis

    Accredited R&D laboratories and custom synthesis firms procure this compound as a reactive precursor in medicinal and material chemistry research. Usage focuses on the elaboration of diverse nitrogenous heterocycles, supporting the exploration of new biologically active scaffolds or electronic materials. Researchers introduce precisely measured aliquots into specialized multistep syntheses under controlled conditions, guided by publication precedents and progress-driven structural verification. This targeted approach upholds both safety standards and research reproducibility.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • Institutional research safety regulations (e.g., OSHA laboratory standard 29 CFR 1910.1450 for US labs)
    • IUPAC nomenclature and characterization guidelines
    • National/provincial permit requirements for piperazine derivatives

    Typical usage ratio

    • 0.02–0.15 molar equivalents per reaction step, with adjustment based on exploratory route and target scaffold size

    Downstream process integration

    • Dosed into sequential cyclization, alkylation, or acylation reactions
    • Reaction run under inert atmosphere with TLC/HPLC monitoring for conversion
    • Post-synthesis workup includes flash chromatography and NMR confirmation

    Final product types

    • Custom heterocyclic research intermediates
    • Investigational structural analogs for pharmaceutical or material science studies
    • Publisable lead compounds subject to subsequent scale-up evaluation
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    Certification & Compliance
    More Introduction

    Understanding 1-(4-Fluorophenyl)Piperazine: Practical Insights from a Chemical Manufacturer

    Direct Experience with 1-(4-Fluorophenyl)Piperazine

    Every batch of 1-(4-Fluorophenyl)Piperazine comes off the line at our production facility after hours of careful synthesis and quality checks because this isn’t a commodity chemical. Its structure—piperazine with a 4-fluoro substituent on the phenyl ring—gives 1-(4-Fluorophenyl)Piperazine a unique place among piperazine derivatives. Our operators and chemists notice differences in handling, stability, and specificity when working with this compound compared to simple piperazine or even 1-phenylpiperazine.

    Material Specifications and What Sets This Product Apart

    1-(4-Fluorophenyl)Piperazine stands out immediately because the presence of fluorine at the para-position alters physical and chemical behavior compared to non-fluorinated analogues. Fluorine’s electronegativity, combined with our precision during synthesis—solid control of temperature, pressure, and purification—yields a crystalline material with high purity. Familiarity with the model, C10H13FN2, helps technicians and our customers track identity and composition, but what matters most in daily use is how the substance behaves in actual practice.

    This material comes as a white to off-white powder, typically with a molecular weight near 180 g/mol, which makes it easy to weigh and handle on scales in both production and laboratory settings. Those small but important physical details—consistency in particle size, stability during storage, and low moisture absorption—help us avoid headaches like caking or inconsistent reactions during downstream applications.

    Application in Research and Industry

    Downstream, 1-(4-Fluorophenyl)Piperazine sees demand mainly in pharmaceutical and advanced organic synthesis. Researchers appreciate its predictable reactivity profile. We watch market and academic literature because every now and then, demand spikes as new intermediates or finished compounds become more important, especially in the development of experimental central nervous system agents, intermediates for complex ring systems, and certain agrochemical molecules. The key in all these cases is the influence of the fluorine atom—it often increases metabolic stability or modulates bioactivity in the desired direction. This isn’t just marketing jargon. Our customers use our material to develop actual molecules, not to fill warehouses.

    Unlike basic piperazine, which finds widespread use as an anthelmintic or in producing polymers, adding the 4-fluorophenyl group changes everything. Organic chemists see different reaction pathways open up, particularly in cross-coupling, substitution, or aromatic ring transformations. Our production line has to account for these requirements, ensuring solvents and catalysts used upstream do not leave traces that could interfere with important synthesis steps down the line.

    Comparisons to Other Piperazine Derivatives

    A lot of people lump piperazines together, but experience teaches that differences between each derivative matter more than datasheets let on. Customers who tried switching between 1-phenylpiperazine, its ortho- and meta-fluorinated analogues, and our 1-(4-Fluorophenyl)Piperazine share stories highlighting issues like reduced yields, solubility problems, or unexpected byproducts. The para-fluoro compound often performs more efficiently in coupling reactions, and it is less prone to certain oxidative pathways that can affect its isomers or non-fluorinated variants. We do not rely on textbook knowledge alone; feedback from long-term partners refining pharmaceutical lead compounds proves this point over and over.

    Imagine an R&D chemist aiming to build a novel library of CNS-active compounds. The decision to use the 4-fluoro over non-fluorinated material often comes down to in vivo data, which can show dramatically better bioavailability or receptor selectivity. 1-(4-Fluorophenyl)Piperazine consistently brings results other analogues just don’t match. Our decision to maintain dedicated production lines, separate from more basic piperazines, grows out of these real differences.

    Stability, Logistics, and Handling Lessons Learned

    Years of working with 1-(4-Fluorophenyl)Piperazine taught us it does not behave the same as bulk commodity amines. The biggest trouble with many aromatic amines comes from oxidation and moisture sensitivity. This product, though stable under normal conditions, still calls for attentive handling—sealed drums, climate-controlled storage, minimized exposure to air during transfer. Every stage, from weighing to packaging, requires good lab and plant practice. Any lapse can knock material out of approved specs, and we address this with real-world solutions: regular purity checks with HPLC and GC, process validation batches, and continuous feedback from customers.

    Our logistics team adapted to support just-in-time manufacturing for pharma customers. That means we run small- to medium-scale batches with short lead times, accommodate specialized container needs, and schedule periodic express shipments if needed. Avoiding bottlenecks comes easily with nimble planning and direct contact with end users—not through layers of resellers diluting accountability.

    Product Development and Continuous Improvement

    We take pride in the process improvements our team has driven on 1-(4-Fluorophenyl)Piperazine. Early on, recrystallization steps produced variable yield and sometimes left residues that complicated further synthetic transformations. Regular cross-talk between synthetic and analytical chemists at our plant pushed us to refine purification columns, increase vacuum control precision, and source higher grade solvents. Results show up in batch consistency and ease-of-use for researchers and process chemists.

    End users notice these improvements. Frequent feedback includes appreciation for the absence of fine particulate dust and the material’s rapid dissolution in both polar and nonpolar solvents. For some, switching to a competitor’s supply forced extra filtration or led to reaction workups with unexpected color changes or solids formation. We document and address specifics with every lot, making data and samples available for trials upon request. Our quality team treats complaints as serious prompts to action, never a nuisance.

    Why Purity and Documentation Drive Value

    The value of 1-(4-Fluorophenyl)Piperazine doesn’t stop at basic purity claims. Analytical transparency builds user confidence. Each lot leaves the facility with HPLC chromatograms, NMR confirmations, and water content checks attached—no ambiguous summaries or barebones paperwork. Regulatory compliance and traceability drives our reputation in the sector.

    GMP compliance attracts the most critical clients. Active pharmaceutical ingredient (API) makers require trustworthy documentation not just for regulatory audits, but to ensure reproducibility and patient safety down the line. We gladly offer additional supporting data when requested and support stability studies for customers scaling up to pilot or commercial production.

    Solving real-world Supply Chain Challenges

    Recent years saw supply chain disruptions reach even specialty chemicals. Pre-pandemic, sourcing intermediates and key starting materials was routine. Now, single-source dependencies and shipping delays mean contingencies matter. We diversified both raw material sourcing and transport partners. Our team mapped alternate transport routes, expanded on-site storage, and pre-qualified a set of domestic and international suppliers for the most sensitive inputs. This allows us to offer reassurance to customers relying on uninterrupted supply.

    Fixed contracts and open communication with both upstream and downstream partners gave us flexibility to pivot. For those relying on just-in-time manufacturing, we take risk mitigation seriously: scheduled reserve stock for strategic clients and open-book access to lot tracking make last-minute orders possible. These measures stem from genuine industry experience, not just a theoretical understanding of logistics.

    Health, Safety, and Compliance Insights

    Manufacturing 1-(4-Fluorophenyl)Piperazine in a facility designed for specialty amines comes with a duty to protect workers and community. On the plant floor, our operators use secure, enclosed systems to minimize exposure. Direct monitoring, periodic health checks, and automated environmental controls form the bedrock of daily safety. Regular training ensures all staff know the specific handling challenges—focusing on dust mitigation, solvent recovery, and emergency response tailored to this substance.

    Safety data sheets, compliance certifications, and export documentation follow every outgoing container, supporting both site and international transport safety rules. We stay current with evolving regulations—like REACH, TSCA, and other country-specific requirements—and respond by adapting internal procedures or customer advisories immediately when conditions change.

    Environmental Commitment

    Minimizing environmental footprint holds a real place in every batch produced. Process solvent recycling, energy management, and scrupulous record-keeping around chemical waste form part of our routine. Green chemistry pushes us to reduce hazardous reagents and maximize atom economy wherever possible. We do this not out of compliance obligation, but because we believe sustainable production matters—and because customers and regulators increasingly demand specific evidence of responsible stewardship.

    Years ago, processing aromatic amines generated costly, difficult-to-treat aqueous waste. Today, we recover and reuse much more solvent and neutralize effluent on-site. Continuous technology review identified safer alternatives to some reagents, reducing not just environmental but also occupational risk. Routine audits by authorities and client representatives confirm our improvements have measurable impact.

    Market Trends and Demand Shifts

    The world does not stand still for specialty chemicals. Demand for 1-(4-Fluorophenyl)Piperazine grew alongside broader interest in fluorinated building blocks for drug synthesis and fully synthetic agrochemicals. Researchers and process chemists look for molecules that combine affordability, functionality, and selective reactivity. Experience tells us the 4-fluorophenyl substituent often checks these boxes better than aliphatic or other aromatic modifications. We track calls for materials that meet increasingly strict impurity profiles and faster delivery windows.

    On the ground, chemists often ask how our product compares to closely related compounds in terms of downstream pharmacological or physicochemical profiles. We respond by pointing to real-world results, not just theory—bioassay results from contract research organizations, comparative studies among CNS-targeted lead compounds, and process robustness in large-scale manufacturing back up our claims.

    Supporting Our Customers Beyond the Product

    Selling quality chemicals is only part of the equation. Our technical support team makes itself available at every step: pre-sale, process development, scale-up, and trouble-shooting. Where an unusual problem with reactivity or solubility arises, our laboratory offers rapid turnaround data or alternative suggestion based on hands-on experience. Knowledge sharing is a two-way street; customer insight leads to product tweaks, packaging improvements, and, occasionally, new material grades altogether.

    Global expansion of R&D, regulatory submissions, and shifting business models in the pharmaceutical and specialty chemical fields mean buyers depend on timely advice and responsive partners. Large and small companies alike benefit from having a reliable supplier of 1-(4-Fluorophenyl)Piperazine who understands technical nuance and market pressures. Our ongoing investments—new reactors, lab automation, staff training—reflect a belief that success lies in always being a few steps ahead of evolving industry needs.

    Summary of Real-World Lessons

    Manufacturing 1-(4-Fluorophenyl)Piperazine takes more than just following a chemistry recipe. Our years of experience taught us to focus on targeted screening of raw materials, exacting controls during synthesis, rigorous purification, and a commitment to transparent communication with every user. We put customer needs first, evolving our processes in step with new scientific discoveries and changing regulatory requirements.

    Whether a customer needs one kilogram for drug discovery or hundreds for scale-up, we see fulfilling their orders as more than a sale—it’s a partnership founded on know-how, adaptability, and a constant push for better performance. Working with this substance every day gives us a perspective few outsiders share, and we aim to keep setting standards others want to match.