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3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid

    • Product Name 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid
    • Alias TFMAP
    • Einecs 683-130-9
    • 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

    834916

    Product Name 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid
    Cas Number 124626-61-7
    Molecular Formula C10H10F3NO2
    Molecular Weight 233.19
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 87-91°C (literature value)
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Storage Temperature 2-8°C (refrigerated)
    Smiles C1=CC(=CC(=C1)C(F)(F)F)CC(C(=O)O)N
    Inchi InChI=1S/C10H10F3NO2/c11-10(12,13)8-3-1-2-7(4-8)5-9(14)6-15/h1-4,9H,5-6,14H2,(H,15,16)
    Synonyms Trifluoromethylphenylalanine
    Pka Approx. 2.1 (COOH), 9.1 (NH2)

    As an accredited 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, HDPE screw-cap bottle labeled "3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid, 25g," includes hazard warnings, batch number, and storage instructions.
    Shipping This product, 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid, is shipped in tightly sealed containers under ambient conditions. Packaging ensures protection from moisture and light. Shipment complies with all relevant chemical transport regulations. Handling instructions and safety data sheet (SDS) are provided. Delivery is available internationally, with transit times depending on destination and customs clearance.
    Storage 3-Amino-3-[3-(Trifluoromethyl)phenyl]propanoic acid should be stored in a tightly sealed container, protected from moisture, light, and incompatible substances. Store at 2–8°C in a well-ventilated, dry area, away from heat and ignition sources. Ensure proper labelling and avoid exposure to strong oxidizing agents. Handle under an inert atmosphere if possible to maximize stability and prevent degradation.
    Application of 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid

    Applications of 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid in Industrial Manufacturing

    As a chemical raw material manufacturer, we support leading industries with 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid. This specialty building block serves advanced synthesis needs in pharmaceutical APIs, agrochemical actives, specialty polymer additives, and fine chemical intermediates. Below, we detail real downstream scenarios based on regulatory, formulation, and processing requirements.

    1. Pharmaceutical API Synthesis: Non-Natural Amino Acid Incorporation

    This compound acts as a non-canonical amino acid for developing novel peptide and small molecule drugs. Drug substance manufacturers use it to introduce trifluoromethyl-phenyl sidechains for target specificity and enhanced metabolic stability. Strict GMP and pharmacopeial compliance controls qualify batch usage. Our monomer integrates into the early solid-phase peptide synthesis or solution-phase coupling, depending on the route. Process chemists adjust raw material feed based on desired substitution and yield optimization. Final APIs include oncology and CNS research actives incorporating fluorinated analogs.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) monograph references for starting materials
    • USP General Chapters on amino acid synthesis

    Typical usage ratio

    • 15–30 mol% relative to the total amino acid content in peptide segments
    • Adjustable on-demand for backbone modification or screening libraries

    Downstream process integration

    • Monomer activation and Fmoc/t-Boc protection for SPPS starting steps
    • Solution-phase peptide coupling for fragment assembly
    • HPLC/crystallization for intermediate purification
    • Integration with scale-up solid-phase reactors and high-volume synthesis lines

    Final product types

    • Small-molecule drug discovery candidates
    • Peptide mimetic APIs for oncology and neuropharmacology research
    • Stable isotope-labeled research compounds
    • High-affinity target binders for diagnostic development

    2. Agrochemical Active Intermediate: Herbicide Synthesis

    Crop protection manufacturers employ this raw material as a structural element in trifluoromethylated phenylpropanoic acid derivatives. It supports the development of herbicidal compounds offering high selectivity in new formulations targeting weed resistance. The ingredient feeds into multi-step synthesis routes requiring reactive amino and carboxyl functionalities for coupling and ring closure. Our supply complies with national agchem legislation and environmental controls. Downstream processors tune charge to activity ratio based on lead molecule design, aiming for target crop/weed specificity. Finished herbicides provide mode-of-action diversity for large-scale agricultural use.

    Industry compliance standards

    • FAO/WHO JMPR specifications on pesticide purity
    • EU Regulation (EC) No 1107/2009
    • EPA FIFRA (40 CFR Part 158) requirements for actives
    • REACH registration for chemical intermediates

    Typical usage ratio

    • 0.8–1.2 equiv/mol per targeted synthetic pathway
    • Determined by ring closure efficiency and herbicide design

    Downstream process integration

    • Condensation or amide coupling in initial actives synthesis
    • Catalyzed cyclization reactions
    • Phase-separation and distillation after product formation
    • Quality monitoring with GC-MS and NMR for product verification

    Final product types

    • Selective post-emergence herbicide actives
    • Trifluoromethylated phenyl herbicide analogues
    • Seedling protection agents
    • Intermediate stock solutions for further formulation

    3. Advanced Polymer Additives: Fluorinated Building Block

    Polymer manufacturers incorporate this acid to introduce fluorine-containing aromatic groups into specialty polymers. The compound modifies hydrophobicity and thermal stability, benefitting advanced engineering plastics and specialty elastomers. The ingredient is dosed by melt-phase or solution blending during polymer backbone formation, with exact levels set to achieve target surface energy or dielectric performance. Quality protocols under ISO 9001/QC batch testing apply. Final compounds improve dielectric insulation or chemical resistance for automotive, electronics, and coating sectors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive (2011/65/EU) for restricted substances
    • REACH compliance for polymer additives
    • ASTM D638 and D257 (tensile and resistivity testing)

    Typical usage ratio

    • 1–5 weight% based on total polymer mass
    • Higher loadings for targeted dielectric/migration resistance

    Downstream process integration

    • Melt or solution-phase addition during monomer weighing
    • Copolymerization in presence of appropriate catalysts and chain transfer agents
    • In-line extrusion or casting for sheet/film production
    • Compound validation by FTIR and surface energy assays

    Final product types

    • Wire and cable insulation compounds
    • Thin-film electronic substrates
    • Fluorinated coating additives
    • Automotive under-hood structural plastics

    4. Fine Chemical Intermediate: Chiral Synthesis & Analytical Reference Standards

    Chemical producers leverage the compound as a chiral auxiliary or reference in asymmetric synthesis and analytical standard preparation. Laboratories and fine chem plants use its aromatic and fluorinated features to generate highly defined stereocenters in process R&D, as well as to calibrate GC/MS and LC/MS systems. The typical process requires precise stoichiometric input, and the compound enters as a protected amino acid or directly in resolution steps. ISO-certified laboratories rely on purity/traceability documentation for analytical lot release and calibrant validation.

    Industry compliance standards

    • ISO/IEC 17025 accredited laboratory systems
    • USP/NF General Chapter <1058> for analytical standards
    • EN ISO 17034 (Reference Material Producers)
    • OECD Guidelines for Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.05–0.2 g per analytical calibration run
    • Up to 0.5–1.5 equiv in chiral center induction steps

    Downstream process integration

    • Weighing under controlled atmosphere for reference standard prep
    • Removal of protective groups during asymmetric synthesis route validation
    • Mixing and derivatization ahead of GC, LC, or NMR calibration
    • In-process purity checks and batch record documentation for traceability

    Final product types

    • Certified chiral reference standards
    • Batch analytical calibration kits
    • Multi-step asymmetric intermediates for research and method validation
    • Process verification blends for regulated QC labs
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    Certification & Compliance
    More Introduction

    3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid: Practical Insights from a Manufacturer’s Experience

    Inside the Reactor: A Hands-On Approach to Quality

    Pulling together a reliable batch of 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid involves far more than just following a recipe. In our facility, experience and discipline guide each step. This compound, known in our process records as model number 3ATFMPP-001, passes through a series of controls that reflect years of improvements and practical know-how. Starting with the first charge of raw materials and extending all the way through packaging, consistency is non-negotiable and every operator in our plant knows the expectation.

    Anyone who’s worked with advanced aromatic amino acids knows that batch-to-batch uniformity can test even the best production lines. With 3ATFMPP-001, visually, it's a solid, off-white powder – an indicator of purity we monitor closely – but true confirmation comes from our analytical equipment. Each lot undergoes HPLC checks and NMR verification as standard, and any deviation triggers a full process review, not just a quick retest.

    The Role of Specifications That Make Sense

    Every lot of 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid leaving our site aligns with specifications established through practical use in competitive chemical markets. We normally target a purity of 98% minimum by HPLC, and moisture content always remains below 0.5%, because excess water content triggers downstream headaches, especially for peptide synthesis. Our team recently reduced trace heavy metal content by refining the wash sequence after the final crystallization. This upgrade responded to direct feedback from customers who witnessed interference in catalytic applications, and it also removed bottlenecks from our own line.

    Melting point, particle size, and solubility are measurements we collect for our own assessment but share with formulators when needed. From a manufacturer’s perspective, material that clumps or absorbs moisture unpredictably always means more unscheduled downtime. Making changes to crystal habit or drying time might seem minor, yet in any plant actually moving multi-kilo volumes, even these details add up to more efficient production for both us and our partners.

    Where Usage Dictates Precision

    Our main clients work in advanced pharmaceutical research, particularly those building on glutamate receptor ligands or beta-aryl amino acids. The trifluoromethyl substitution at the meta-position changes electron distribution, and chemists leveraging this effect must trust their building blocks. Failures tend to trace back to minute, overlooked variations, so we choose not to blend lots – each drum carries a single batch number and its own certificate, so records actually match reality.

    Besides life sciences, this compound finds use in crop protection research due to its ability to mimic structural motifs present in bioactive molecules. We’ve seen a recent increase in demand from agrochemical labs working on novel herbicide leads, since the compound brings both hydrophobic bulk and metabolic stability. Our operators sharpened up procedures just to keep up with tighter delivery schedules during these upswings, building a buffer stock so projects do not stall out waiting for key intermediates.

    Some research teams also incorporate this amino acid into novel polymers. The CF3 group influences both reactivity and final material attributes, which in turn changes how companies can tweak their end products. The benefit from our side comes from repeatable, well-understood material – nobody really wants to troubleshoot downstream surprise reactions due to supplier shortcuts.

    Comparing with Analogues: Not All Amino Acids Are the Same

    Over the years, we’ve made several substituted propanoic acids, experimenting with various aromatic, halogen, and alkyl groups. Each tweak brings its own quirks in synthesis and purification. Focusing on the trifluoromethylphenyl-derived version, the difference comes down to both chemistry and scaled practicality. Across our runs, the inclusion of the CF3 group at the 3-position has distinct implications: it pushes the pKa down and impacts the reactivity at the alpha-carbon, which plays out during subsequent peptide bond couplings or chiral separations. Polyester variations lacking the trifluoromethyl group had higher byproduct formation and lower yields for particular alkylation steps. Anyone who has tried to swap out amino acids in a medicinal chemistry series knows how sensitive these systems can be to the electronics and sterics of each substituent. Each material comes with its own handling demands; our trifluoromethylated compound stores well, staying free-flowing in standard drums, while some more basic aryl versions tend to absorb ambient moisture and cake up.

    There’s a reason clients keep returning for this specific structure. In bioactive molecule development, small differences translate to measurable shifts in pharmacokinetics and interaction profiles. Our scientists track not only traditional QC data, but also how our batches perform in real-world syntheses. We regularly survey partners for feedback, feeding findings straight back to our process engineers.

    Addressing Challenges Our Customers Face, Directly from the Plant Floor

    Among the everyday concerns for labs using 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid, solubility and analytical reproducibility top the list. Years ago, researchers explained that lot-to-lot variability in raw materials was disrupting key steps, especially during compound registration runs. Our response involved running tighter intervals on both particle size distribution and drying end-point, after observing how much these shifts influenced solution-making and storage.

    Another repeating conversation centers on contamination. Our experience underlines that even parts-per-million of certain residuals can knock an entire sequence off balance. One direct improvement sprang from input by a customer working under regulatory standards, who encountered unexplained peaks on their HPLC at relatively early stages. Our follow-up checks uncovered a previously unnoticed byproduct from an early synthetic loop — an issue solved by slightly adjusting the acid workup regime and integrating a double filtration. These kinds of operational fine-tuning matter, because missed detail at the source magnifies headaches downstream.

    Nobody enjoys chasing down mystery spots on an NMR. Our standards are built around rooting out even trace-level process impurities, and our operators hold batch sheets for every step, so retracing any issue becomes possible. Over time, we’ve adopted split-batch retention, keeping material from every drum archived for at least 18 months. It was not always mandatory, but seeing real-world lab needs, we found extra documentation pays for itself.

    What Stability and Shelf Life Really Mean in Practice

    From raw storage rooms to field conditions, we observe that the stability of this compound stands up well compared to related amino acids. We keep drums at ambient temperature, shielded from light and excess humidity. Over the course of 12 months, our internal retests confirm key markers, including minimal changes in melting point and no drift in assay results. Clients with longer inventory cycles ask for retest data beyond a year, so we routinely extend our testing schedule. Real stability comes from both the synthetic strictness upstream and the physical protections during filling and shipping. It’s not glamorous work, but these routines keep surprises to a minimum both here and for those using our product down the line.

    We see warehouse bulk regularly withstand periods of unintended excessive warmth, especially during the summer, with no apparent degradation. Still, for high-integrity work, lab benches prefer sealed environments. So our final packaging step double-bags the material and seals drums with tamper-evident bands, eliminating sources of moisture and cross-contamination.

    Logistics and Consistency in the Real World

    Every batch of 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid spends a day or two on our shipping prep station undergoing spot checks, because skipping this step brings risks of supply chain disruption. We’ve experienced firsthand how weather and transit delays can disrupt predictable access to specialty materials, so in direct response, we expanded our on-site inventory to buffer regular customers.

    Handling and filling at scale presents a unique set of mechanical challenges. Over time, our team fine-tuned powder transfer methods to minimize airborne particles, learning by trial and error how powder flow changes with each new batch size. Today, we employ both anti-static liners and careful drum-tapping to achieve clean dispensing. Unplanned spills or improper fillings not only waste finished product but also hamper later lot tracing. Each of these operational lessons feeds into what ends up on the shipment pallet, and our customer service team keeps real communication lines open about any non-standard handling request.

    For clients combining our compound with other rare amino acids, we accommodate custom pack sizes. Multi-kilo drums suit industrial labs, but we break down lots to single-kilo containers for those mapping out exploratory reactions. Each package leaves with identifiable handling tokens, so researchers know immediately which lot supports which synthetic step.

    Investing in Collaborative Solutions

    Sourcing high-value building blocks for pharmaceutical and materials science research takes real trust. We dedicate process improvements to real-world feedback, not just metrics pulled from certificates. Every enhancement – whether an extra filtration step, or a repolish of our packaging line to reduce static – arises from hard-won lab experience.

    Our core advantage rests on direct communication with end-users. One example stands out: a collaboration with a biotech company refining their lead compound structure. They needed not just delivery on a timeline, but open access to our process documentation and willingness to field technical questions. Our process chemists and production specialists sat in on weekly troubleshooting calls, sharing NMR spectra and synthetic notes, not just shipment bills. This mutual transparency advanced not just their research, but also deepened our own understanding. The lessons we drew from this partnership are now built into our regular process reviews.

    Our perspective means prioritizing practical, not theoretical, solutions. If a client highlights a recurring bottleneck, we troubleshoot directly, rather than pushing a solution that looks good on paper but stalls out in scale-up. The manufacturing floor remains our primary feedback loop, and every team member knows their daily work carries downstream consequences.

    Realities of Sourcing: Navigating a Challenging Raw Material Market

    Raw material costs have become less predictable over the past year. We’ve weathered sudden spikes in fluorinated intermediate pricing, which tested both our forecast models and supply relationships. We keep a stable vendor base, vetting every new supplier with qualification runs before making any sourcing decisions. This careful vetting means we avoid cheaper imports that risk inconsistent impurity profiles or packaging problems. It has paid off in fewer batch failures and better reliability for partners depending on us for tight timelines.

    We have also invested in stockpiling key sensitizers and stabilizers. That decision reflects not just cost hedging, but the blunt reality that critical research depends on uninterrupted supplies. Our purchasing department works directly with our plant technical group to review contracts and storage needs every quarter, adjusting so gaps in supply are unlikely. Any time a missed delivery triggers a slowdown, we investigate at the process level, then reformulate our approach if necessary.

    The Human Touch: Why Operator Skill Shapes Product Reliability

    Sophisticated equipment helps, but the single best safeguard for quality comes from the people running each process. Our most experienced operators routinely spot subtle color shifts or unexpected crystal shapes that no automated probe picks up. Teams keep logs documenting all anomalies, reviewing these notes each shift. The practical difference shows in the feedback from customers who note how much smoother their workflows go when using a batch from our facility.

    Training continuously evolves. New staff shadow our lead operators and learn direct observation-based protocols for assessing critical process thresholds. This approach retains the “muscle memory” that our team has accumulated over years of real-world operational runs.

    Connecting Manufacturing Decisions to Real Applications

    As research trends shift, the requirements for building blocks change, and what worked for last year’s process might not match this cycle’s needs. Our direct line to ongoing research means adjusting particle size or enhancing purity not just as an abstract goal, but to anchor the performance reality researchers expect. We collect real application feedback and use it to refine process details.

    For firms developing small-molecule drugs or advanced polymers, having a reliable supply of a functionalized amino acid like 3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid means fewer process delays and better data clarity. Missing or inconsistent batches do more than tie up schedules—they sometimes derail entire drug target programs or material science evaluations. By keeping our own manufacturing practical, open, and responsive, we support customers’ research, not just with a product, but with a collaborative partnership.

    What Sets Manufacturer-Direct Supply Apart

    Over years supplying this amino acid, we continually hear from clients who switched away from brokers or third-party resellers. The reason usually involves issues with traceability, outdated paperwork, or lots that arrive looking and performing differently than expected. Direct lines between our plant and customer chemists keep transparency high—every question about process, impurity profile, or batch data gets a documented answer, not a generic file.

    Customers leverage our in-house documentation, real-time lab support, and willingness to do technical dives on process questions. These manufacturer-level connections set the foundation for trust and routine success in time-sensitive, high-stakes research environments.

    Shaping the Future: Compound Quality and Research Progress

    3-Amino-3-[3-(Trifluoromethyl)Phenyl]Propanoic Acid earned its place in highly specialized research because of consistent performance, well-characterized impurity profiles, and the practical insight gained from running repeated manufacturing lots. As the market evolves, we remain committed to refining process details, incorporating customer feedback, and investing in staff training to ensure product reliability. The only constant is the demand for reliability, and delivering that comes from lived experience, focus on process, and direct engagement with both the plant floor and the chemists putting our material into action.