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5-(4-Fluorophenyl)Valeric Acid

    • Product Name 5-(4-Fluorophenyl)Valeric Acid
    • Alias 5-(4-Fluorophenyl)pentanoic acid
    • Einecs 617-261-8
    • 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

    669173

    Chemical Name 5-(4-Fluorophenyl)valeric acid
    Molecular Formula C11H13FO2
    Cas Number 242478-37-1
    Appearance White to off-white solid
    Melting Point 56-60°C
    Boiling Point 332.4°C at 760 mmHg
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=CC=C1CCCC(=O)O)F
    Inchi InChI=1S/C11H13FO2/c12-10-6-4-9(5-7-10)3-1-2-8-11(13)14/h4-7H,1-3,8H2,(H,13,14)
    Storage Conditions Store at room temperature, in a dry and well-ventilated place

    As an accredited 5-(4-Fluorophenyl)Valeric Acid 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 25 grams of 5-(4-Fluorophenyl)valeric acid; sealed with screw cap and labeled with hazard and handling information.
    Shipping 5-(4-Fluorophenyl)Valeric Acid is shipped in secure, sealed containers suitable for chemical transport. The packaging ensures protection from moisture and contamination. Shipping complies with relevant chemical transport regulations, including labeling and documentation. Temperature and handling instructions are provided as necessary, ensuring safety and integrity throughout transit to the destination.
    Storage 5-(4-Fluorophenyl)valeric acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight. Ensure it is clearly labeled and out of reach of unauthorized personnel. Follow local regulations and consult the safety data sheet for additional handling and disposal guidelines.
    Application of 5-(4-Fluorophenyl)Valeric Acid

    Applications of 5-(4-Fluorophenyl)Valeric Acid in Industrial Manufacturing

    5-(4-Fluorophenyl)valeric acid plays a defined role as a specialty raw material in advanced synthesis, with application primarily anchored in pharmaceutical intermediates, agrochemical precursor synthesis, and custom material manufacturing sectors. This section details specific downstream applications based on confirmed usage, providing industry practitioners with focused insight into requirements, process integration, and finished product outputs.

    1. Synthesis of Anticonvulsant Drug Intermediates

    This chemical finds a specialized use as a building block in the development of novel anticonvulsant agents where substituted valeric acid derivatives serve as core intermediates. Industrial customers employ the acid in targeted condensation or amidation steps, contributing structural and physiochemical properties necessary for late-stage drug substance modification prior to final salt formation or crystallization, ensuring batch consistency and regulatory conformity.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • ICH Q3A, Q3C impurity control guidelines
    • United States Pharmacopeia (USP) for intermediate testing protocols
    • FDA 21 CFR Part 210/211 (where exported APIs are involved)

    Typical usage ratio

    • 3–15% molar ratio in intermediate coupling reactions; adjusted according to desired side chain length and target API yield requirements

    Downstream process integration

    • Added during the acylation or alkylation step after aromatic precursor formation; monitored for purity via HPLC before downstream transformations, such as esterification or amide bond formation

    Final product types

    • Active pharmaceutical ingredient (API) intermediates for anticonvulsant candidates and related CNS drug substances

    2. Intermediate for Fluorinated Agrochemical Synthesis

    Major agrochemical producers utilize this raw acid in the preparation of advanced herbicide and pesticide intermediates where the fluorophenyl moiety enhances biological activity and environmental stability. Utilization typically focuses on introducing the aromatic-fluorine unit into the molecular scaffold during late-stage process development, supporting robust structure-activity profiling and patentable product innovation.

    Industry compliance standards

    • FAO Specifications for Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • EU REACH Regulation (EC) No 1907/2006
    • ISO 9001 for chemical quality management

    Typical usage ratio

    • 1.5–6% by weight in precursor synthesis; adjusted for product series and batch scale-up trials

    Downstream process integration

    • Enters as a core reactant during fluorinated aromatic chain extension, post-coupling condensation with amines or alcohols to form ester or amide agro-intermediates; purification via column chromatography prior to active ingredient synthesis

    Final product types

    • Herbicide active ingredient intermediates
    • Insecticidal precursor compounds
    • Patent-protected fluorinated crop protection agents

    3. Custom Material Synthesis for Specialty Polymer Modifiers

    Engineered materials manufacturers integrate this acid into functional monomer synthesis to impart unique fluorinated aromatic characteristics required in advanced polymers used for specialty coatings and adhesives. The raw material alters the polymer backbone for improved chemical resistance and controlled flexibility, with precise addition timing critical for reproducible copolymer performance and regulatory certification for industrial and technical applications.

    Industry compliance standards

    • ISO 14001 (environmental management)
    • Directive 2011/65/EU (RoHS for certain technical end-uses)
    • ASTM D638, D882 (mechanical property testing of polymers)
    • REACH Authorisation Annex XIV for fluorinated chemical controls

    Typical usage ratio

    • 0.25–2% by weight in copolymerization or post-polymerization functionalization; optimized through lab-scale trials for final mechanical property targets

    Downstream process integration

    • Introduced at the copolymerization or end-group modification phase, followed by extrusion, film casting, or resin compounding; QC testing for residual monomer and functional group incorporation

    Final product types

    • Fluorinated polymer additives for coatings
    • Specialty flexible adhesive resins
    • Chemical-resistant engineering thermoplastics

    4. Intermediate for Research-Grade Synthetic Reagents

    Manufacturers supplying research and diagnostic reagent houses adopt this compound as a core constituent in novel enzyme inhibitors, labeling reagents, and analytical standards. Integration into synthesis starts with the fluorinated phenyl chain extension, conferring precise molecular recognition features for small-scale reference materials and analytical method development, particularly within regulated research environments.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 (testing and calibration laboratories)
    • OECD GLP for advanced reagent development
    • European Pharmacopoeia—reference substance protocols

    Typical usage ratio

    • 1–7% by weight as a functional group donor; tailored to synthesis route and desired reference material purity

    Downstream process integration

    • Used during early-stage functionalization of custom reagents, including amidation, esterification, or labeled compound derivatization; monitored via NMR and LC/MS before downstream packaging

    Final product types

    • Research-grade enzyme inhibitors
    • Custom-labeled analytical reagents
    • Certified reference substance kits for laboratory QC
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    Certification & Compliance
    More Introduction

    Introducing 5-(4-Fluorophenyl)Valeric Acid: A Reliable Building Block from a Trusted Manufacturer

    Getting to Know 5-(4-Fluorophenyl)Valeric Acid

    Sourcing 5-(4-Fluorophenyl)Valeric Acid directly from the manufacturer takes the guesswork out of process chemistry. Our direct experience producing this compound means we can share more than just numbers on a TDS. The unique substitution pattern of this molecule, with a fluorine at the 4-position of the phenyl ring, creates interesting reactivity and physical properties that influence how it behaves in real-world synthesis.

    Over the years, we have refined manufacturing approaches to offer this acid in consistent quality. Each batch passes through rigorous checks—identity, purity, moister control, and residual solvent evaluation—before it leaves our facilities. Chemists working in pharmaceutical intermediates, agrochemical development, and advanced materials know batch variation can add headaches down the line. Reliable control of the critical attributes that matter in real process work, including the physical appearance, melting point, and solubility, is something we stand behind batch after batch.

    It’s More Than a CAS Number

    Chemists searching by registry numbers sometimes miss the nuance among similar molecules. Tweaking the position of a fluorine atom on the aromatic ring—not to mention changing its alkyl chain length—can alter a compound’s usefulness. Our 5-(4-Fluorophenyl)Valeric Acid delivers a blend of hydrophobicity and molecular weight that fits a surprising range of synthesis needs, filling gaps left by the more common benzoic or acetic acid analogs. 4-fluoro substitution on the phenyl group isn’t merely a curiosity; it modulates electron density in ways that influence coupling reactions or downstream derivatization.

    This molecule stands apart from alternatives such as non-fluorinated valeric acid derivatives or those with different halogen positions. In our experience, substituents like chlorine or bromine bring distinct reaction profiles and hazard profiles. Fluorine’s subtlety—a small atomic size, strong bond energy—can give better thermal and chemical stability during scale-ups, which supports cleaner downstream transformations for the medicinal chemist or process developer chasing purity at every step.

    Handling and Storage Insights from the Production Floor

    As a chemical manufacturer, controlling every detail matters. Raw materials for 5-(4-Fluorophenyl)Valeric Acid synthesis demand close attention, since minor impurities sneak in easily and can complicate scale. Our process trains operators and chemists to look for clues—color, clarity, minor odors—that might point to side-reactions or, more rarely, contamination risks. With repeated production runs, we have learned the best ways to minimize loss during crystallization and drying, cut down on unnecessary exposure, and use the optimal grade of solvents.

    Freshly isolated product stores best in tightly sealed containers, protected from direct sunlight and humidity. The molecule’s robustness to light surprises many, perhaps owing to the aromatic ring and stable fluoro group, but ambient moisture will still cause slow hydrolysis over time if left unchecked. For that reason, we recommend keeping storage below 30°C and opening larger drums only in well-controlled environments. Secondary packaging adds protection against air transfer and avoids problems with caking or clumping, preserving its free-flowing nature for easy transfer.

    Why End-Users Turn to Direct Manufacturers for This Acid

    Large pharma labs and smaller process houses approach us because our technical support goes well beyond quoting a purity figure or shipping a drum. We’ve seen chemistries where even 98% assay is not enough—where a trace amount of certain aromatic byproducts throw off a late-stage transformation requiring a ruthenium or palladium catalyst. That’s why our internal specifications look at not only purity by HPLC/GC, but profile the impurity fingerprint too, so uncommon peaks don’t surprise our downstream partners.

    Our technical know-how helps process teams plan for the nuances of scale-up. Many customers bring us their pain points, whether it’s a crystallization that yields needle-like, hard-to-filter crystals, or solubility issues in their chosen solvent system. Our process chemists run similar scenarios frequently in the lab and production floor, using this direct feedback to improve our control. Because we’ve seen what can go wrong, we adapt our protocols—sometimes changing reflux profiles, crystallization temperatures, or solvent combinations accordingly. People value this insight because it brings predictability to their R&D, not just commodity pricing.

    The Value of Consistency in Production Scale

    Scale is where the gulf between casual synthesis and real-world manufacturing shows most clearly. More than once, we've worked through challenges where upscale from 100 gram lots to tens-of-kilos brought unexpected byproducts, simply because the heat profiles shift and local concentrations increase. It’s easy to miss at lab scale, but the fluorophenyl group’s behavior shifts as volumes climb.

    Thermal sensitivity and handling during neutralizations, phase separations, and extractions all show up as challenges in production. By keeping every nuance logged in our batch histories and adapting our recipe based on accumulated plant-floor knowledge, we catch drift and course-correct rapidly. Feedback from our partners helps us tweak and document process parameters—agitation speeds, filtration method, and drying profiles all factor into the final lot characteristics.

    Customers who’ve had disappointing lots from resellers—those where color, purity, or even just packing were inconsistent—realize the difference that our approach brings. We’ve invested in modern analytical equipment: NMR, LC-MS, and Karl Fischer titration help us pin down out-of-spec material before it becomes a customer issue. The result is a consistently higher rate of accepted lots, which means less downtime chasing replacement material.

    How 5-(4-Fluorophenyl)Valeric Acid Fuels Innovation

    Research chemists and formulators see clear differences between this acid and standard valeric or benzoic acids during lead optimization phases. The 4-fluorophenyl motif turns up as a favored group in pharma libraries designed to improve metabolic stability and receptor binding. Its carbonyl group, set apart by a flexible pentanoic chain, means users can introduce the core moiety through a host of chemistries—amidation, Suzuki or Sonogashira coupling, or Friedel–Crafts type acylations.

    We see strong demand for this building block in drug discovery pipelines as well as in the early stages of scale-up for new agrochemical leads. Researchers often choose this molecule for introducing subtle changes in molecular models, especially where bioactivity screens point to fluorine as a driver of selectivity or in vivo stability. From conversations with our major customers, lead series that failed with other aromatic acids sometimes find renewed promise with this particular analog, which supports more robust SAR studies.

    In materials science, this acid functions as a flexible linker or precursor for engineered polymers and specialty intermediates. Its semi-flexible C5 spacer and fluoro-aromatic moiety allow it to slot into designer monomer families, lending sought-after hydrophobic and structural features. We routinely support partners running exploratory batches for specialty coatings, optoelectronic device prototypes, and advanced adhesive additives.

    Addressing Sustainability: Realistic, Stepwise Improvements

    A question we hear more often these days: “How sustainable is your process for this acid?” Chemical synthesis, especially for fluorinated compounds, faces extra scrutiny over waste generation and reagent selection. We’ve responded with real changes on the plant floor. Process audits push us to recover and reclaim solvents like THF and DMF wherever purity standards allow. Wastewater is treated through in-house units designed specifically for aromatic acid residues, with effluent streams monitored for trace halides.

    We’ve transitioned away from more hazardous fluorination reagents, focusing on starting materials that show greater atom economy and reduced by-product formation. In addition, batch reaction temperatures are optimized to reduce overall energy consumption—important both from a cost and CO2 impact point of view. The process for 5-(4-Fluorophenyl)Valeric Acid now runs cleaner than our workflows from even five years ago, which aligns with corporate and industry shifts toward responsible manufacturing.

    Sustainability isn’t just a compliance box for us. Long-term relationships with customers mean transparent information sharing about the resources, energy, and risks associated with the molecule’s lifecycle. By listening to our clients’ own sustainability mandates, we adapt packaging volumes, offer greater technical detail on origin and fate of reagents, and develop protocols for safe handling and waste minimization at the user’s site. In this way, the value of a direct manufacturer comes through—no hidden steps, no vague supply chain risks—just clear knowledge you can build on.

    The Differences Only Manufacturers Notice

    If you’re using similar acids sourced from traders and happen across issues—batch-to-batch color variation, odd odors, unexpected solubility quirks—that’s no accident. Subtle differences in crystalline habit or trace impurity carry-over stem from control deficiencies upstream. We’ve seen new customers dismiss these “small” differences, only to come back after project delays or downstream equipment fouling force a change. A pure supply chain, firmly under the manufacturer’s control, removes these risks.

    As a manufacturer, every tweak in process or batch record gets field-tested before it becomes standard. The learning curve for this particular acid means even small changes to crystallization timing or filter media can drastically reduce downstream confusion with off-white samples or inconsistent melting behavior.

    Working from the raw materials onward, our technical teams adjust feeds based on the real reactivity of each batch of starting fluoro-aryl intermediates, since even minor fluctuations in their assay can modify final crop and purity. This sort of problem-solving doesn’t show up on a spec sheet, but it makes the difference on the bench and in the plant.

    Regulatory and Quality Perspectives

    Advanced pharmaceutical, agricultural, and electronic products must answer to demanding regulatory requirements. From the moment a partner signals their intended use—whether for clinical, pre-clinical, or field studies—we put supporting documentation in place. Traceability flows from the earliest raw material intake through the final sealed drum, so our end-users never guess where a given lot originated.

    Quality systems oversee the entire process: in-process analysis, cleaning validation, and material movement. We also support technical submissions with certificates of analysis backed up by infrastructure-level QA audits, not mere paperwork. For clients in North America, Europe, and Asia, clear regulatory pathways and predictable timelines stem from the thoroughness of our quality management infrastructure. Genuine traceability and transparent data win our customers time and again.

    Supporting Research and Manufacturing Development

    Customers tackling challenging syntheses can tap into our direct process experience. New clients often phone in with a handful of technical questions: “Will this crystallize cleanly from IPA?” or “Have you seen side-reaction x crop up under basic hydrolysis?” Drawing from years of batch notes, our technical team walks through what has—and hasn’t—worked for similar transformations.

    This partnership style means academic labs, process chemists, and industrial formulators gain more than just material. If a client runs into agitation, filtration, or drying problems, our manufacturing chemists can help troubleshoot with in-plant parallels. Access to this knowledge makes all the difference when running at kilo or multi-kilo scales, replacing theoretical data with hard-earned process specifics.

    For teams developing new routes, we offer small custom lots through to larger scale production with rapid lead times. This flexibility means experimental work isn’t held up waiting for fresh supply, and results reflect the performance of the actual material destined for production, not just a one-off gram-scale lot. Over time, our partners value the technical continuity, as early learning translates into reliable supply once projects move to launch or pilot plant scale.

    R&D Synergy: Building on Downstream Insights

    Continuous two-way communication with end-users has shaped the way we produce and supply this molecule. Many innovations in our process start with a technical problem shared by a customer, whether that’s a solubility challenge in a specific solvent, or unpredictable yields during late-stage coupling. Each time, we consult production and R&D teams to see how modifications could tackle the root cause—sometimes as simple as a tweak in filtration protocol or as complex as introducing a new purification step.

    Periodic technical exchanges add more value to both sides—users get best practices on preparation and use, while we get real-world feedback on emerging needs in process design, regulatory adaptation, or application optimization. In pharma or materials pipelines, every small gain brings projects closer to throughput and cost targets.

    Practical Applications: Experiences from Our Customers

    Projects in crop science development often require novel aromatic acids for synthesis of bioactive molecules. This acid’s 4-fluoro-substituted structure makes it well suited for producing intermediates where subtle changes in electron density matter. In a recent case, one partner was able to streamline late-stage synthesis steps simply by substituting in our material—improving both yield and product isolation.

    For teams working on new solid-phase peptide linkers, the combination of a relatively flexible five-carbon chain and the rigid fluoro-aromatic unit made for improved linker geometry and purity. Downstream results included easier purification and cleaner characterization data. Our technical support played a role here, offering crystallization and drying tips during scale-up.

    Specialty polymer developers have also taken advantage of the unique motif, using 5-(4-Fluorophenyl)Valeric Acid as a functional monomer or end-group modifier. Increased resistance to hydrolysis over time, attributed to the fluorinated aromatic, meant more stable products in coated films and adhesives. Adoption of our bulk packaging reduced handling hazards and wastage, thanks to the consistent bulk handling characteristics of our material.

    In Summary: The Manufacturer’s Commitment

    Providing 5-(4-Fluorophenyl)Valeric Acid as a manufacturer means embracing every step, from the chemistry behind the synthesis through to the practical realities of shipping, support, and sustainability. Decades of hands-on experience and customer feedback show that superior control creates a better-performing, safer, and more predictable product. Behind every drum is a technical team ready to answer questions, suggest solutions, and adapt production to fit evolving needs.

    As end-users adopt new projects, knowing that their raw materials are backed by genuine expertise, transparency, and strong process control gives confidence that their work can progress without unexpected setbacks. That’s our commitment with every delivery of 5-(4-Fluorophenyl)Valeric Acid—crafted through direct experience, offered with practical insight.