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3-(3-Fluorophenyl)Propionic Acid

    • Product Name 3-(3-Fluorophenyl)Propionic Acid
    • Alias 3FPPA
    • Einecs 663-083-2
    • 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

    280914

    Chemical Name 3-(3-Fluorophenyl)propionic acid
    Cas Number 13146-17-9
    Molecular Formula C9H9FO2
    Molecular Weight 168.17
    Appearance White to off-white solid
    Melting Point 62-65°C
    Smiles C1=CC(=CC(=C1)F)CCC(=O)O
    Inchi InChI=1S/C9H9FO2/c10-8-4-2-3-7(6-8)5-1-9(11)12/h2-4,6H,1,5H2,(H,11,12)
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place; keep container tightly closed

    As an accredited 3-(3-Fluorophenyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 3-(3-Fluorophenyl)propionic acid comes in an amber glass container with a secure screw cap and clear labeling.
    Shipping 3-(3-Fluorophenyl)Propionic Acid is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Proper labeling and documentation are included to comply with chemical transport regulations. Handle with care, using appropriate PPE, and store in a cool, dry, well-ventilated area during transit to ensure product stability and safety.
    Storage Store **3-(3-Fluorophenyl)propionic acid** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure all containers are clearly labeled, and access is restricted to trained personnel. Use suitable secondary containment to prevent accidental spills.
    Application of 3-(3-Fluorophenyl)Propionic Acid

    Applications of 3-(3-Fluorophenyl)Propionic Acid in Industrial Manufacturing

    As a core building-block intermediate, 3-(3-Fluorophenyl)Propionic Acid supports demanding downstream production needs in the pharmaceutical, agrochemical, and fine chemical markets. Below we outline its commercial-scale applications where this material’s purity, controlled reactivity, and consistent supply anchor major product lines for our global B2B clients.

    1. Non-Steroidal Anti-Inflammatory Drug (NSAID) Intermediate Production

    Manufacturers of next-generation NSAIDs integrate 3-(3-Fluorophenyl)Propionic Acid as a key synthetic precursor during the active pharmaceutical ingredient (API) stage. The compound’s aromatic fluorination facilitates targeted functionalization in streamlined multi-step reactions—primarily via amide coupling or esterification—enabling differentiation in pain management drugs and anti-inflammatory agents. Batch records track this intermediate from warehouse receipt through validated reactor charging and crystallization. Analytical controls verify impurity thresholds before API isolation, as set by global regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP Guideline for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • Chinese Pharmacopoeia Monograph
    • EU EudraLex Volume 4 GMP, Annex 13 (APIs for Clinical Use)

    Typical usage ratio

    • Typically 1.0–1.3 molar equivalents per API target batch
    • Adjustment based on step-wise yield (<98%) and reagent purity assessments

    Downstream process integration

    • Charged during Stage 2–3 of API synthesis for NSAID analogs (e.g., amide bond formation with substituted anilines or pyridines)
    • Integrated into downstream purification via recrystallization or preparative chromatography

    Final product types

    • Branded and generic anti-inflammatory tablets and capsules
    • Pain relief topical gels and ointments
    • Veterinary oral suspensions

    2. Herbicide and Plant Growth Regulator Intermediate

    Leading agrochemical formulators use this fluorinated aromatic acid as a synthetic unit in the manufacture of selective herbicides and plant growth regulators. The propionic acid group undergoes activation to corresponding acid chlorides or esters, participating in selective acylation reactions to produce active ingredients with enhanced metabolic stability for pre- and post-emergent weed control. Production lines routinely verify supply chain traceability, and batch processing includes inert atmosphere handling to limit hydrolysis during derivative formation.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Evaluations
    • US EPA 40 CFR Part 180 (Tolerance Levels)
    • ISO 9001:2015 Quality Management—Agrochemical Manufacturing
    • China GB 2763 (Food Safety National Standard: Maximum Residue Limits)

    Typical usage ratio

    • 0.2–0.6 molar equivalents per herbicide target compound
    • Ratio fine-tuned to mitigate formation of process byproducts

    Downstream process integration

    • Fed into initial condensation step for substituted phenylpropionate herbicides
    • Processed via continuous flow reactors to synthesize acylated actives

    Final product types

    • Formulated herbicide granules and soluble concentrates
    • Plant growth regulator emulsifiable concentrates (EC)
    • Seed treatment coatings with phenylalkanoic derivatives

    3. Advanced Liquid Crystal Intermediate for Display Materials

    3-(3-Fluorophenyl)Propionic Acid features in specialized syntheses for high-performance liquid crystal intermediates, playing a crucial role in constructing mesogenic cores with tailored dielectric and optical properties. Its introduction into aromatic ring systems via Friedel-Crafts acylation or Suzuki coupling enables downstream diversification in television and display panel manufacturing, ensuring precise refractive index control and stability under prolonged use. Formulation teams document all starting material batch numbers as part of ISO-based quality protocols.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Display Material Synthesis)
    • IEC 61747 (Flat Panel Display International Standard)
    • RoHS Directive (2011/65/EU) for hazardous substance limitation
    • Japanese Chemical Substances Control Law (CSCL)

    Typical usage ratio

    • 0.1–0.4 molar ratio per mesogenic core structure
    • Calculated against target molecular weight of liquid crystal mixture

    Downstream process integration

    • Introduced in step-wise coupling during aromatic core assembly
    • Followed by purification via flash chromatography or distillation

    Final product types

    • Thin-film transistor (TFT) LCD display panels
    • Specialized temperature-compensated liquid crystal mixtures
    • Monomer blends for OLED and flexible display components

    4. Synthesis of Fluorinated Aroma and Flavor Building Blocks

    In fine chemical synthesis for fragrance and aroma houses, this propionic acid derivative acts as a key intermediate in constructing fluorinated aromatic blocks, imparting stability and distinctive note modulation in high-value flavors. Esterification or amidation with chiral auxiliaries during downstream processing preserves desired olfactory characteristics while meeting tight food safety controls. All intermediates pass through dedicated purification units to eliminate cross-contaminants and align with food additive purity demands.

    Industry compliance standards

    • US FDA 21 CFR 172.515 (Flavoring Substances)
    • EU Regulation (EC) No 1334/2008 (Flavourings and Food Ingredients)
    • IFRA Global Fragrance Regulation
    • FEMA GRAS certification (Flavor and Extract Manufacturers Association)

    Typical usage ratio

    • Usually 0.08–0.2 weight % in the final flavor/aroma compound library
    • Usage scaled for targeted sensory threshold and regulatory compliance

    Downstream process integration

    • Entered in early-stage esterification as a fluorinated extender group
    • Processed via batchwise or continuous stirred reaction systems before blending

    Final product types

    • Food-grade flavoring additives for beverages and candies
    • Fine fragrance accords for personal care and home products
    • Stabilized aroma blends for specialist industrial uses (e.g., air care systems)
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    Certification & Compliance
    More Introduction

    3-(3-Fluorophenyl)Propionic Acid: A Practical Look from the Plant Floor

    Practical Introduction to 3-(3-Fluorophenyl)Propionic Acid

    Every chemical that rolls off our production lines tells a story, and 3-(3-Fluorophenyl)propionic acid stands out for more than just its mouthful of a name. Its CAS number (771-99-3) tags it for the scientifically minded, but what else sets this compound apart in real-world manufacturing? Let's break down its character, why it draws steady orders from repeat customers, and what users point out once they start working with it.

    Our Manufacturing Experience

    On a typical week, batches of this molecule pass through reactors built for precision. Our team grew up working hands-on with aromatic acids, and the learning curve on handling fluoroaromatic intermediates brings specific quirks: one cannot rush the halogenation steps, and the controlled addition of the fluorine group needs calm operators. Over time, we’ve tweaked our process to keep quality steady—temperature control gets obsessive and purification rounds can feel endless, but clean product with consistent melting point and purity still depends on those details.

    Maintaining a tight process window, we routinely check purity by HPLC and NMR so that the material heading out of the door suits our partners’ synthesis needs. Residual solvents? Out. Environmental controls? More than an afterthought. Our staff know that chemists in the next link of the chain prefer material they can trust batch after batch.

    Specifications and Handling

    3-(3-Fluorophenyl)propionic acid lands on the dock white to off-white—the color tells us a bit about trace impurities, and we batch-release at a minimum 98% purity. The product stays stable under dry, light-protected storage, but humidity makes it clump, so we double-seal every bag for shipment. Large lots keep granularity manageable for dosing, a point we've learned matters to technicians who don't want headaches with every scoop.

    Crystallinity signals a cleaner sample: this acid melts around 44–46 °C, which means it doesn’t clog up standard feeders or pumps. Such simple, robust specs keep supply chains smoother, and fewer process adjustments downstream mean satisfied chemists and production managers.

    Usage in Pharmaceutical and Agrochemical Synthesis

    We see most interest from partners working in pharmaceutical intermediate synthesis. That fluorine ring isn’t just for show—it’s prized for metabolic stability. Adding a fluoro group influences bioavailability, a trick medicinal chemists exploit when building drugs with tunable half-lives or altered toxicity. Our feedback comes less from textbook examples and more from direct conversations: a synthetic chemist once remarked at a trade show how, after switching to our acid, his yields in a key anti-inflammatory intermediate jumped by 3%. Nobody’s claiming miracles, but small boosts make a difference in high-value drug work.

    Outside pharma, crop science teams order steady quantities for herbicide and fungicide development. Here, the stability granted by the fluorine bond gives longer activity in the field, and propionic acids like this stand up well under exposure to sunlight and water. The knock-on effect—fewer field applications—matters for both farm budgets and regulatory compliance.

    Distinctive Features Compared to Related Acids

    Every producer with a propionic acid line gets requests to match profiles, but 3-(3-fluorophenyl)propionic acid holds up its end in a few ways. Compared to non-fluorinated analogs (like 3-phenylpropionic acid), the presence of the fluorine atom really does alter key reaction pathways—both in basic chemistry and in biological targets. For those using it as a building block, this means higher selectivity in some transformations, and different pharmacokinetic properties for lead optimization.

    Against its ortho- and para-fluorinated siblings, the meta isomer isn’t just a casual choice. Med-chem teams sometimes switch between isomers to tune a compound’s electron density or binding profile. Our meta-fluoro version finds use where the para or ortho position proved too reactive (or not reactive enough) for downstream steps. In our own process labs, we notice the shift in reactivity especially during coupling reactions for new candidates.

    Critical Process Lessons over the Years

    We didn’t arrive at our process overnight. Early batches struggled with halogen introduction—yield suffered until we slowed exothermic steps and kept water under tighter control. Now, we chart every parameter from raw material origin to post-purification filtration, minimizing batch-to-batch drift. It’s common sense, but nobody understands chemical production like those who’ve had to dig residue out of a clogged filter press after a missed endpoint.

    Environmental controls run deep with substances like this. We minimize mother liquor disposal and recover solvents for repeat cycles to keep both emissions and costs in check. Waste gas treatment addresses any trace fluorinated organics, and we train teams to handle spills with rapid containment to prevent small leaks from leading to larger headaches down the road.

    Quality Management and Customer Feedback

    Consistency gets you return business. Customers expect a spec, and deviations—even one-off—travel fast. Trace differences in melting point or a slightly pale tint raise red flags for folks running validated syntheses where one bad lot sets back weeks of work, and we have heard the frustrations firsthand. Our experience says: small investments upstream prevent costly disputes and product returns later.

    Before releasing lots, QC labs run full identification, in-process checks confirm identity by infrared and NMR, and content is verified by titration or HPLC. Our own teams use this material internally for reference synthesis, so we keep samples frozen for cross-comparison if any lot ever gets questioned down the line. A bulky inventory of reserve samples has rescued more requalification requests than we care to admit.

    Open lines with technical clients help, too. Incoming feedback, both positive and constructive, shapes batch documentation and spurs process tweaks. Operators in our plant have sat through more than one customer audit. Sharing best practices and lessons learned—whether about moisture limits, carrier solvents, or packing methods—lets us spot improvements well ahead of any complaint letter.

    Supply Chain and Packaging Lessons

    Transporting organic acids in bulk means headaches if you aren't careful: rough handling crushes crystals, leading to dustier product and dosing errors, so we use heavy-duty polyethylene liners and hard-walled containers. Customers working with microreactors or automated dispensing have mentioned blockages with differently made batches from past suppliers, but our QA feedback loop and controlled granule sizing cut down on these problems.

    Sealing methods stem from lessons learned during humid shipping seasons—double bags, desiccant pouches, and immediate transfers prevent moisture-driven caking. It’s not glamorous, but no one wants to hack apart a hardened block of acid in a production suite.

    Regulatory and Environmental View

    Fluorinated organic acids carry environmental responsibilities. Regulations shift fast, and countries have differing standards. Our facility committed to best-in-class emissions controls: those steps mean lining up with major international certifications and local outreach for community safety. Internally, we keep regular training on spill response and personal protective equipment.

    Because some jurisdictions scrutinize fluorinated substances more closely, our documentation stays updated and we field regular questions from compliance officers. We share third-party analysis upon request, including absence/presence tests for residual solvents or heavy metals—a need we overlooked years ago until a regulatory audit caught us understaffed.

    Technical Support and Long-Term Relationships

    Supplying a stable product wins repeat orders, but long-term users ask deeper questions: “How does your acid act in Grignard couplings?”, “Does your process introduce trace metals affecting my catalyst life?”, “Have you run stability trials past 12 months?” Our technical support team doesn’t live in a call center—the same chemists who scale up lots help draft application notes, and join conferences or video calls to solve customer bottlenecks.

    Joint R&D projects pop up, too. Not long ago, we worked with a customer scaling a new pharma intermediate. Tweaks in crystallization and dryer dwell time led to sharper melting points, less dust, and more reliable feeding in their reactor train. Shared learnings drove both their project and our next process tweak. Such hands-on collaboration sets expectations on both sides and drives the iterative progress we value.

    What We've Learned from Comparisons

    Users who have worked with a range of aromatic propionic acids tell us the differences aren’t academic. Fluorination in the meta spot delivers better metabolic stability in vivo without some of the reactivity headaches that para placement causes. Chemists running library syntheses value ease of purification. In feedback surveys, some users switched to our meta-fluoro material after frustration with supply gaps on ortho products, and stayed for the consistent crystallinity.

    Every time we evaluate possible process changes, we benchmark analytical data from a range of suppliers, including those who favor ortho or para substitutions. Our focus is keeping side products low and purification straightforward, especially for customers running high-throughput synthesis or under tight timeframes.

    Challenges and Adaptations in Real Production

    Producing specialty acids at scale isn’t about switching on a machine. Raw material quality fluctuates, so we source from long-term partners who understand why small variations in fluorobenzene grade lead to big downstream troubles. Sometimes, extra steps in solvent recycling or additional charcoal treatments make a difference between a pass and a fail on product color.

    Operator discipline means fewer deviations, so we invest time in training and rigorous checklists. These habits get built not from rulebooks, but from real situations where a moment’s inattention led to a whole batch falling shy of spec.

    Occasionally, users want custom particle sizing or higher specification on trace contaminants; we respond by running experimental batches and recording outcomes, adapting production or packaging as real usage data accumulates.

    Trusted Experience from the Manufacturing Line

    Years of shipping 3-(3-Fluorophenyl)propionic acid to labs and plants around the world give us a grounded view: the compound matters for both its structural value and its consistent, dependable performance across applications. Not everything about its production is glamorous, and pitfalls hit those who cut corners on purification or ignore feedback from the plant floor. Other analogs work in some places, but meta-fluorination strikes a balance many synthetic chemists prefer for stability and selectivity. Quality management, regulatory readiness, and technical support shape the experience our long-term partners rely on.

    For all its chemical intricacy, the story of this molecule reads like most good plant-floor tales: keep your hands clean, tools sharp, and lines open, and users will keep coming back for the product that works—batch after batch.