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2-(Trifluoromethyl)-Dl-Phenylalanine

    • Product Name 2-(Trifluoromethyl)-Dl-Phenylalanine
    • Alias DL-3-(Trifluoromethyl)phenylalanine
    • Einecs 249-617-2
    • 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
    VTB
    Specifications

    HS Code

    850289

    Productname 2-(Trifluoromethyl)-Dl-Phenylalanine
    Casnumber 102817-56-3
    Molecularformula C10H10F3NO2
    Molecularweight 233.19
    Appearance White to off-white powder
    Purity Typically ≥98%
    Meltingpoint 126-130°C
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Smiles FC(F)(F)c1ccc(cc1)CC(N)C(=O)O
    Boilingpoint Decomposes before boiling
    Storagetemperature 2-8°C
    Opticalactivity DL (racemic mixture)
    Synonyms α-(Trifluoromethyl)-DL-phenylalanine
    Inchi InChI=1S/C10H10F3NO2/c11-10(12,13)7-3-1-2-6(4-7)5-8(14)9(15)16/h1-4,8H,5,14H2,(H,15,16)

    As an accredited 2-(Trifluoromethyl)-Dl-Phenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Glass amber bottle labeled "2-(Trifluoromethyl)-Dl-Phenylalanine, 5g" with hazard symbols and product details, securely sealed and boxed.
    Shipping 2-(Trifluoromethyl)-DL-Phenylalanine is typically shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. The package is labeled in accordance with regulations for safe transport and may require temperature control. Shipping complies with local and international chemical safety guidelines, including appropriate documentation and hazard information if applicable.
    Storage 2-(Trifluoromethyl)-Dl-Phenylalanine should be stored in a tightly sealed container, protected from light and moisture. Keep the chemical at a cool, dry, and well-ventilated location, ideally at 2–8°C (refrigerator). Ensure it is kept away from strong acids, bases, and oxidizing agents. Clearly label the container and follow all standard laboratory safety and storage protocols.
    Application of 2-(Trifluoromethyl)-Dl-Phenylalanine

    Applications of 2-(Trifluoromethyl)-Dl-Phenylalanine in Industrial Manufacturing

    Our facility produces high-purity 2-(Trifluoromethyl)-Dl-Phenylalanine for specialized applications in pharmaceutical research, peptide synthesis, chiral catalyst manufacture, and advanced agrochemical development. Supported by rigorous quality control and compliant production protocols, we supply this fluorinated amino acid to leading downstream manufacturers who demand both traceability and reliability in their formulation chains.

    1. Pharmaceutical Research and Early-Stage API Synthesis

    Researchers and pilot-scale pharmaceutical producers employ this advanced building block to introduce trifluoromethyl moieties into investigational new drug (IND) candidates, targeting small molecule therapeutics where fluorination modulates biological activity or metabolic stability. Sourcing directly from our site ensures full batch traceability and consistent stereo- and regiochemical purity, which is crucial during route scouting and scale-up of APIs under ICH and pharmacopeial guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)
    • Ph. Eur., USP, JP reference monographs (where fluorinated amino acid analogues are registered)

    Typical usage ratio

    • 0.2–2 mol% relative to total amino acid building blocks in lead synthesis routes; adjusted according to targeted fluorination sites within the molecule’s structure-function map

    Downstream process integration

    • Introduced during early-stage solution-phase or solid-phase assembly of peptide-based APIs; frequently as a coupling partner via standard peptide bond formation protocols (e.g., HATU, EDCI/HOBt chemistry); batches undergo intermediate QC for stereochemical integrity and purity

    Final product types

    • Preclinical and early clinical phase drug candidates containing fluorinated aromatic rings
    • Research grade peptidomimetic APIs for pharmacokinetic evaluation

    2. Peptide and Protein Engineering

    Our material finds specialized use in synthetic peptide manufacturing and protein chemistry labs engaged in engineering enhanced bioactivity and novel protease resistance. Site-specific incorporation of the trifluoromethylated amino acid expands the chemical diversity of biologics, often for in vitro enzyme studies or biophysical stability enhancement projects. Manufacturers prefer our low-metal, low-residual solvent grades for minimizing background interference in downstream protein folding and purification steps.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management Systems for research peptide manufacture
    • Synthetic peptide cGMP production rules, including EudraLex Volume 4 (EU GMP Guidelines)

    Typical usage ratio

    • 1–10 equivalent substitutions per 100 amino acid residues, depending on sequence engineering requests and aggregation behavior in downstream folding

    Downstream process integration

    • Used as a direct Fmoc- or Boc-protected amino acid monomer input within peptide synthesizers (SPPS); post-coupling, side chain deprotection steps utilize mild acidic conditions to preserve the fluoroaromatic group

    Final product types

    • Modified peptides for protease stability assessments
    • Engineered proteins for drug delivery research or diagnostic reagents

    3. Chiral Auxiliary and Organocatalyst Manufacturing

    Chemical manufacturers in the field of asymmetric synthesis employ our fluorinated amino acid in proprietary chiral ligand and organocatalyst production lines. The trifluoromethyl group impacts not only electron distribution but also enhances catalyst selectivity, particularly in enantioselective hydrogenation or aldol reactions. We deliver tight specification lots, allowing reproducible stereocenter formation and minimizing by-product contamination for catalyst formulators scaling to kilo-lot outputs.

    Industry compliance standards

    • ISO 9001:2015 (Chemical Intermediates Manufacturing)
    • REACH (EC) No 1907/2006 Registration for advanced intermediates

    Typical usage ratio

    • 0.5–5 mol% as a component of chiral ligand frameworks, varied according to the transformation’s selectivity profile and batch scale

    Downstream process integration

    • Enters the synthetic step of chiral ligand backbone building before derivatization; subsequent catalyst formation steps integrate metal complexation or ionic functionalization using the phenylalanine core structure

    Final product types

    • Chiral phase-transfer catalysts for asymmetric transformations
    • Specialized chelating ligands for pharmaceutical fine chemicals synthesis

    4. Agrochemical Active Ingredient Research

    Agrochemical R&D departments utilize this fluorinated amino acid as a molecular scaffold when developing crop protection compounds with improved metabolic and environmental profiles. The material enables structurally diverse analog screening where electron-withdrawing trifluoromethyl groups alter target binding and soil degradation kinetics for candidate pesticide molecules. We supply custom lot specifications for formulation trial labs adhering to regulatory pesticide research protocols.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025:2017 Accredited Analytical Laboratories
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market

    Typical usage ratio

    • 0.1–1.5 molar equivalent within early-stage analog synthesis libraries; tuneable based on lead optimization and structure-activity modeling outputs

    Downstream process integration

    • Incorporated during target compound assembly via Suzuki-Miyaura or amide coupling reactions on mg–g lab scales; typically used prior to salt formation or formulation with surfactants for biological activity tests

    Final product types

    • Candidate crop protection active ingredients for field residue and efficacy trials
    • Lead scaffolds for herbicide and fungicide discovery projects
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 2-(Trifluoromethyl)-DL-Phenylalanine: Purpose-Built for Modern Research and Manufacturing

    From the Bench to Production: Our Commitment to Chemical Integrity

    Manufacturing specialty amino acids challenges even the most experienced chemists, especially when it comes to compounds like 2-(Trifluoromethyl)-DL-Phenylalanine. Through direct control of every aspect of synthesis, purification, and quality testing, we put reliability at the center of our work. This compound does not blend in with the handful of generic derivatives found in catalogs—both structure and performance set it apart and justify ongoing investment in our tight process control.

    Focusing on Details: Composition and Consistency

    2-(Trifluoromethyl)-DL-Phenylalanine stands out with the presence of the trifluoromethyl group at the ortho position on the aromatic ring of the core phenylalanine structure. We synthesize the racemic mixture, balancing both D-and L-enantiomers, because our customer base spans both preclinical researchers and developers of new pharmaceuticals or agrochemicals. Fluorination at the 2-position impacts both electronic and steric properties, which can improve metabolic stability and binding properties in target molecules. This molecular tweak may look simple on paper, but carrying out a clean, scalable synthesis that maintains high enantiomeric purity every day requires decisive attention to raw material traceability.

    Over the years, we've learned that laboratories want to work with authentic material—a batch-to-batch match in melting point, purity, and particle profile. Synthesis always begins with fluorinated benzaldehyde, passing through a well-honed sequence to introduce the amino acid side chain. Our typical specification exceeds 98% HPLC purity, and our QA team uses proton and fluorine NMR, along with LC-MS and IR, to confirm structure and exclude trace contaminants.

    Since suppliers often cut corners through adapting cheaper precursor steps or reducing the rigor in crystallization, end users of those materials face erratic analytical outcomes or unexpected process upsets. During one incident in our own pilot line, a switch of a purification solvent made the difference between a product suitable for peptide synthesis and one full of micro-level residues. Only vigilant process engineering can make sure the final compound supports both gram-scale and multikilogram demands. Traceability down to individual drum lots means any question gets resolved in the lab, not at the end user's bench.

    Applications Rooted in Evolving Research

    Researchers and formulators who choose 2-(Trifluoromethyl)-DL-Phenylalanine expect more than molecular building block functionality. Our technical team regularly hears from peptide drug researchers who incorporate the compound to optimize ligand-receptor selectivity or alter in vivo half-life. The ortho trifluoromethyl group offers enhanced electron-withdrawing characteristics, inevitably improving aromatic stacking and sometimes introducing unique hydrogen bond acceptor capacity, all without disturbing the core features of the scaffold. These benefits translate into either tighter binding affinity or expanded metabolic robustness in drug discovery, giving medicinal chemists a customizable tool for SAR studies.

    Beyond drug development, agrochemical teams rely on high-purity, fluoroaromatic amino acids as part of lead molecule construction and property tuning. Agricultural constraints on residue tolerances and off-target environmental effects require non-negotiable documentation of every step in synthesis. We saw one client’s greenhouse trial nearly derailed by the unseen fluorescent impurity in a third-party competitor’s shipment—an impurity level that seemed negligible until deleterious side effects appeared in their field results. Seeing that incident affirms our investments in extended analytical screens and storage conditioning, ensuring our product supports both regulated and experimental projects without caveats.

    What stands out for biochemists is the compound’s compatibility with standard peptide coupling, as well as new methods under microwave or solid-phase conditions. The trifluoromethyl motif does not introduce problems seen with many sulfonic or nitro analogs. For high-throughput screening, the robustness of our DL-analogue helps teams run large, variable assays with fewer false positives and less batch-to-batch drift.

    Comparative Advantages Over Other Fluorinated Phenylalanines

    Experience in the factory exposes practical differences between grades of phenylalanine derivatives. Direct feedback from users points out shortcomings in other products, such as uncontrolled moisture uptake or unexplained color drift, which can impact both research and production yield. Many standard fluorinated amino acids, like 4-fluorophenylalanine or 3,5-bis(trifluoromethyl)-phenylalanine, alter electron distribution differently, and tend to disrupt the aromatic ring’s interaction with target proteins in unpredictable ways. Our 2-(trifluoromethyl) variant keeps the aromatic system intact, nudging physical and biochemical outcomes in the right direction.

    In situations where teams compare our offering to unspecialized commodity versions, small points—like absence of residual solvent, guaranteed reproducibility of melting profile, or confirmation of trace metal absence—sway the outcome. Over years of forthright dialogue with our users, the value of a direct line between production and bench-side troubleshooting stands out more than any line item on a technical data sheet. Our production logs rarely see adjustments because we design each batch using in-house-developed SOPs tailored from actual customer feedback, not stock approaches.

    Environmental and Operational Responsibility

    Chemical manufacturing must step up to stricter sustainability and safety requirements. Over the last decade, persistent environmental pressures shaped both our process design and our standards for waste management. Working with highly fluorinated intermediates brings safety and disposal challenges, but we've invested heavily in closed-loop solvent recovery and on-site acid neutralization. This discipline means that downstream users never have to wonder about the origin or stewardship of their intermediate.

    Responsible chemistry calls for more than just compliance. We publish our process safety data with complete lifecycle analysis, and every outgoing drum of 2-(Trifluoromethyl)-DL-Phenylalanine ships with detailed batch analytics, not only basic COAs. We built our solvent extraction stages around lessons from earlier years, when competitor product recalls spurred us to redesign and automate every step of filtration, concentration, and final drying. Today’s platform grew out of relentless improvement in process containment—non-negotiable for any partner pursuing green chemistry or low-footprint manufacturing targets.

    Fighting Shortages and Ensuring Future Supply

    Inconsistent supply chains for specialty chemicals threaten both research timelines and commercial output. Our own experience during semiconductor fluorine shortages and interrupted logistics during pandemic shutdowns cemented our dedication to holding raw material inventory and expanding redundant synthesis lines. These investments matter every time a forecast changes or when seasonal spikes in demand put pressure on fluoroaromatic feedstocks.

    One lesson stands out: scalable, responsive manufacturing allows project leaders to commit to tight milestones. Our forecast models draw from real historical usage, not speculative reselling patterns. Orders placed directly with us trigger production queueing, never cross-dock flips. This approach means that production never gets delayed by an intermediary trying to force MOQ splits or sitting on aging stock. Our regular users have direct points of contact with chemists and production managers, guaranteeing both technical consultation and clear timelines.

    Building Dialogue with the Scientific and R&D Community

    Much of our knowledge evolves at the hands of customers who push boundaries in medicinal, agricultural, and biochemical research. Our doors remain open to collaboration, whether someone wants insight on scale-up from grams to kilos or targets downstream property tweaks through isotopic labeling or enantiopure resolution. The best advances arise when manufacturing sits shoulder to shoulder with discovery. Recent months saw our technical team work alongside peptide developers to address solubility bottlenecks during test batch formulation, not through off-the shelf answers, but process-adapted tweaks born from close listening.

    Direct relationships are essential. Our technical support never routes through call centers or email filters. Both researchers and procurement managers know they speak to process-side staff with authority to explain method or discuss troubleshooting. We believe answers grounded in firsthand factory experience outpace any FAQ or templated troubleshooting document. That attitude knit together a user base comfortable sharing error scenarios, innovation needs, and regulatory changes directly with us—allowing us to remain nimble and honest about what is possible in each batch.

    Learning from Complications: Process Ownership and Open Communication

    Mistakes and holdups teach lessons not found in textbooks. Years ago, we responded to complaints from an early-stage API client frustrated by unexplained retention time shifts during peptide mapping. Our audit dug past standard deviations and pinpointed a micro amount of trifluoroacetate, introduced during a late-stage crystallization. That event drove us to overhaul how we select and audit auxiliary agents used in every batch. This feedback loop built credibility, not only with that client, but in the methods we now offer to every downstream user.

    Direct accountability keeps us evolving. By discussing real process and method decisions in open forums and audits, we build mutual trust with researchers and regulatory partners. Every year brings a round of challenges, whether that’s switching to new greener solvents, adopting higher resolution analytical methods, or trialing alternatives for fluorinated starting materials as regulations shift. Our conviction remains that every material leaving our doors has to meet the ambitions of evolving science while demonstrating stewardship for workers and the environment.

    Future Directions: Building on Experience

    The needs of R&D and manufacturing will not slow down. As research into protein targeting, metabolic engineering, and receptor-specific ligand development advances, the demand for complex amino acids with purposeful side chain substitution grows. We continue to invest in new routes and formulation options for 2-(Trifluoromethyl)-DL-Phenylalanine: micronized powders, custom particle engineering, lot size flexibility, and options for isotopic or chiral enrichment. These improvements respond directly to scientist feedback and scale-up data accumulated in-house, not through generic industry trends.

    Our methods, from the first reaction setup through the last QA sign-off, are documented, reproducible, and always open to audit by the researchers whose discoveries depend on chemical reliability and transparency. We learned, sometimes painfully, that shortcuts backfire. Pressure from production quotas or supply chain hiccups cannot be allowed to undermine the integrity of scientific research or product development. For us, long-term value always traces back to maintaining a steady supply of materials that serve both today’s needs and tomorrow’s innovation.

    Summary: A Direct, Committed Approach to Chemical Supply

    2-(Trifluoromethyl)-DL-Phenylalanine reflects what dedicated chemical manufacturing should be: precise, responsive, and grounded in open conversation with the community that relies on it. Our team draws on decades of experience to bridge the gap between the factory floor and the research bench. Acting as the actual manufacturer—not an intermediary—means accountability runs through every stage, from raw material to final user.

    This product grew out of a direct commitment to meeting the high standards of researchers and formulation scientists. Our ongoing challenge shapes each batch: to deliver chemical consistency with practical, real-world support, strengthening the link between reliable supply and scientific advance.