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3-Fluoro-L-Tyrosine

    • Product Name 3-Fluoro-L-Tyrosine
    • Alias 3-Fly
    • Einecs 629-014-3
    • 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

    187838

    Product Name 3-Fluoro-L-Tyrosine
    Chemical Formula C9H10FNO3
    Molecular Weight 199.18 g/mol
    Cas Number 700-16-3
    Appearance White to off-white solid
    Melting Point >200 °C (dec.)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8 °C
    Optical Rotation [α]20/D +13 to +15° (c=1, H2O)
    Synonyms 3-F-Tyr, 3-Fluorotyrosine
    Smiles NC(CC1=CC(F)=CC=C1O)=O

    As an accredited 3-Fluoro-L-Tyrosine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 3-Fluoro-L-Tyrosine (1 gram) is a sealed amber glass vial, labeled with product details and safety information.
    Shipping 3-Fluoro-L-Tyrosine is shipped in secure, airtight containers to prevent contamination and moisture exposure. The package is labeled according to chemical safety regulations and includes documentation for handling and storage. Temperature conditions are maintained as required, and all relevant safety data sheets accompany the shipment for compliance and user safety.
    Storage 3-Fluoro-L-Tyrosine should be stored in a tightly sealed container at 2-8°C (refrigerator), protected from light and moisture. It should be kept in a dry, well-ventilated area, away from incompatible substances. Follow standard laboratory chemical storage protocols, using appropriate labeling and secondary containment to prevent contamination or accidental release. Always refer to the Safety Data Sheet (SDS) for specific storage recommendations.
    Application of 3-Fluoro-L-Tyrosine

    Applications of 3-Fluoro-L-Tyrosine in Industrial Manufacturing

    As a direct manufacturer with years of fine chemical synthesis experience, we supply 3-Fluoro-L-Tyrosine for specialized applications where precise molecular modification is crucial to downstream product integrity and regulatory compliance. Our material supports a limited but deeply technical range of fields driven by stringent quality and traceability requirements. Below, we detail representative industrial use cases, highlighting each scenario’s compliance landscape, typical incorporation levels, integration stage in manufacturing, and final product forms as practiced by industry clients.

    1. Active Pharmaceutical Ingredient Synthesis (Peptide Drug Manufacturing)

    3-Fluoro-L-Tyrosine serves as a non-natural amino acid building block for the site-specific introduction of a fluorine atom in peptide-based drug candidates. During solid-phase peptide synthesis (SPPS), this raw material allows peptide manufacturers to improve metabolic stability and modify pharmacokinetic profiles for new molecular entities registered with health authorities. Quality and batch control are governed by pharmacopeial guidelines and cGMP regulations throughout the production chain.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP & EP Monographs (where applicable for intermediates)
    • FDA 21 CFR Part 210/211 (for API and peptide drug production)
    • EDQM, EMA/CHMP specifications for raw materials in APIs

    Typical usage ratio

    • Customarily 1–2 equivalents per fluorinated residue in target peptide; precise ratio determined by peptide sequence and desired substitution pattern, typically ranging 1–10% by peptide molar content.

    Downstream process integration

    • Charged at protected-amino acid coupling stage during SPPS cycle; post-coupling deprotection, resin cleavage, and downstream purification follow established peptide workflow.

    Final product types

    • Investigational and commercial peptide APIs (oncology, metabolic disease drugs)
    • Peptide research tools for pathway analysis and mechanistic studies
    • Diagnostic peptides for in vitro kits

    2. Stable Isotope Labeling for Medical Imaging Probes

    This fluorinated amino acid acts as a precursor in synthesizing PET tracers and radiolabeled imaging agents, targeting amino acid uptake and metabolism in tissue diagnostics. The fluorine atom in 3-Fluoro-L-Tyrosine is leveraged in conjunction with isotopic exchange or direct labeling chemistry, producing imaging probes for non-invasive disease evaluation under highly regulated radiochemical production environments. Manufacturing must be validated against both GMP and radiopharmaceutical safety standards.

    Industry compliance standards

    • GMP for Investigational/Clinical Radiopharmaceuticals (EU/EudraLex Volume 4)
    • USP Chapter <825> (Radiopharmaceuticals—Preparation, Compounding, Dispensing, and Repackaging)
    • FDA/EMA/ANSM guidelines for radioactive substances
    • ISO 13485 (where imaging agents form part of a device system)

    Typical usage ratio

    • Stoichiometric amounts as defined by precursor to target compound, generally 3–8% of total substrate batch in labeling protocols; ratio flexes based on tracer yield and clinical dose requirements.

    Downstream process integration

    • Introduced at the chemical synthesis stage prior to radiolabeling or direct isotopic incorporation; post-processing involves purification, QA/QC release testing, and formulation for injection.

    Final product types

    • 18F-labeled tyrosine analogs for PET imaging (oncology diagnostics)
    • Experimental diagnostic tracers for metabolic and neurological disorders
    • Reference materials for radiochemical method validation

    3. Protein Engineering and Structure–Function Studies (Biotech Research Supplies)

    Biotechnology research teams employ 3-Fluoro-L-Tyrosine to generate site-specifically modified proteins in recombinant systems. By incorporating this analog at pre-determined residue positions, researchers probe the effects of fluorinated side chains on protein folding, interaction, and stability, which is essential for structure–activity relationship (SAR) studies. Our GMP-compliant supply chain ensures traceability for critical academic and industrial research under certified laboratory standards.

    Industry compliance standards

    • ISO 9001 (Quality Management Systems for research reagent supply)
    • OECD GLP (Good Laboratory Practice for non-clinical research)
    • Material Safety Data Sheet (MSDS) disclosure per local regulations (REACH, OSHA-GHS)
    • Chain of custody requirements (for documentation in regulated projects)

    Typical usage ratio

    • Media supplementation at 0.1–2 mM concentration for bacterial or cell-free expression; ratio adjusted based on codon usage and aminoacyl-tRNA synthetase specificity.

    Downstream process integration

    • Added during protein expression in engineered strains or cell-free extracts; residue incorporation confirmed by mass spectrometry or NMR at the protein QC stage.

    Final product types

    • Fluorinated recombinant proteins for X-ray crystallography or NMR analysis
    • Molecular probes for biophysical stability experiments
    • Reagent-grade biomaterials for academic and industry-focused studies

    4. Precursor for Custom Fluorinated Chemical Reagents

    As a specialty synthesis intermediate, 3-Fluoro-L-Tyrosine is valued by custom chemicals manufacturers developing small-molecule reference compounds for pharmaceutical and biotech validation. By serving as a starting point for further substitution or functional group transformation, this material underpins downstream creation of fluorinated aromatic scaffolds, supporting SAR optimization projects in regulated analytical settings. Material traceability and batch homogeneity remain critical in these workflows.

    Industry compliance standards

    • ISO 9001/ISO 14001 (Quality and Environmental Management)
    • REACH Regulation (EU) 1907/2006 (for EU-based production or supply)
    • Material traceability requirements under GHS/CLP for chemical intermediates
    • Analytical standard certification (where end-use requires reference quality)

    Typical usage ratio

    • Batch-dependent; often 5–15% of reaction feedstock based on target scaffold yield and downstream modification efficiency.

    Downstream process integration

    • Undergoes derivatization (e.g., halogen exchange, side-chain modification) during early-phase custom synthesis; isolated intermediates are purified and characterized for downstream use.

    Final product types

    • Custom chemical intermediates for medicinal chemistry
    • Research and analytical standards for pharmaceutical R&D
    • Building blocks in advanced organic synthesis workflows
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    Certification & Compliance
    More Introduction

    3-Fluoro-L-Tyrosine: A New Level of Precision in Amino Acid Chemistry

    Introducing 3-Fluoro-L-Tyrosine Straight from the Production Floor

    The market often sees new variants of amino acids claiming unique advantages, but 3-Fluoro-L-Tyrosine has earned its position through tangible advances in peptide synthesis and biomedical research. Our years in chemical manufacturing underscore the fact that small molecular changes drive vast improvements in reactivity, selectivity, and compatibility with demanding lab environments. We chose to focus on 3-Fluoro-L-Tyrosine after seeing its direct impact on both R&D and scale-up processes in peptide and protein science.

    At the bench, scientists have long searched for ways to expand the natural toolbox of amino acids. By introducing a fluorine atom to the aromatic ring, 3-Fluoro-L-Tyrosine gives researchers freedom to study protein folding, enzyme function, and signal transduction with new precision. Today it finds its place in both classic peptide assembly lines and modern drug discovery.

    Direct Production, Rigorous Control

    As a direct producer, we control the process from raw input through to finished product, which brings two clear benefits: reliable purity and true insight into every batch’s behavior under diverse conditions. Our team manages every reaction, isolation, and quality check. Our 3-Fluoro-L-Tyrosine appears as a white crystalline powder, and each lot passes a comprehensive final inspection. Routine checks analyze purity by HPLC, confirm molecular identity with NMR and MS, and verify enantiomeric excess with chiral chromatography. Years handling shipments to research labs and manufacturing floors have taught us that consistency cannot be left to chance.

    Through our experience during scale-up, minor modifications in solvent choice or work-up shift final yield and residual impurity profile. Only direct, hands-on process knowledge allows tight management of these parameters. This depth of experience comes through when customers bring technical questions or unexpected analytical results—they rarely face issues we haven’t seen and tackled before.

    Applications Shaped by Frontline Research

    Researchers use 3-Fluoro-L-Tyrosine as a building block in solid-phase peptide synthesis, labeling studies, and as a probe for protein structure. The single fluorine atom stands in for hydrogen at the 3-position of the tyrosine ring, creating subtle electronic effects without major steric interference. This property makes it invaluable for understanding intramolecular interactions and mapping active sites, far surpassing what standard tyrosine can offer.

    In academia and industrial labs, chemists insert 3-Fluoro-L-Tyrosine into synthetic peptides and proteins to deepen understanding of biochemical pathways or to enhance pharmacokinetic profiles for therapeutic candidates. The fluorinated analog remains close enough to the parent amino acid to preserve biological function in most cases, but grants clear insights under ^19F-NMR or mass spectrometry due to the unique labeling effect. This single edit at the atomic scale unlocks data that would otherwise remain obscured.

    Companies exploring kinetic isotope effects or protein-protein interactions benefit from the specific electronic properties that fluorine introduces. These research directions demand high-purity materials since trace impurities or off-isomers distort detection and quantitation. Our control over absolute stereochemistry—maintaining the L-configuration—means that results reflect the intended experiment, not batch-to-batch variability.

    Real-World Challenges in Manufacturing: Not All 3-Fluoro-L-Tyrosine is the Same

    Skills learned from years at the reactor bench reveal where material differences matter. Minor missteps lead to issues like partial racemization, introduction of positional isomers, or trace solvent residues. Each of these influences the performance of 3-Fluoro-L-Tyrosine in demanding research. Many resellers and traders lack direct insight into what comes off their shelves, but direct producers like us know the subtleties that impact downstream applications.

    For example, moisture control in final product handling makes a visible difference in stability and appearance. Slight residual solvent can skew HPLC traces, but precise drying and storage protocols prevent these headaches. Our daily routines include not just analytical testing, but real engagement with process improvements. Where some run into sticky powders or mixed polymorphs, our approach yields a product chemists can depend on, from the first gram to the last kilogram.

    These details come out in customer feedback as well. Labs often mention the challenge of synthesizing reliable peptides when input amino acids aren’t pure and homogeneous. A direct manufacturer has the incentive—and the experience—to address these factors at the source.

    Differences from Tyrosine and Other Fluorinated Analogs

    Chemists sometimes assume all tyrosine analogs behave similarly, but substitutions at different positions or by different atoms lead to profound differences in reactivity, biological effects, and spectroscopic profiles. 3-Fluoro-L-Tyrosine differs in key ways from natural tyrosine, 4-fluoro-tyrosine, and other halogenated derivatives.

    The fluorine at the 3-position alters electron density around the aromatic ring. This modulates activity in enzymatic reactions—phosphorylation, oxidation, and nitration respond differently compared to unmodified tyrosine. This allows researchers to probe specific steps in protein metabolism or to freeze labile intermediates for observation.

    Compared to 4-fluoro-tyrosine, the meta position influences hydrogen bonding and ring orientation in distinctly different patterns. Peptide chemists exploit this to alter peptide structure or modulate receptor binding affinities. The limited size and high electronegativity of fluorine make it less disruptive than larger halogens and offer a balance of change without wholesale disruption of protein function.

    Our lot-to-lot testing confirms that the L-stereochemistry stays intact—a detail missed by some who rely solely on supplier declarations. This situation plays out in collaborations with pharmaceutical researchers who cannot afford to repeat syntheses due to off-target isomer content. Through direct experience, we have learned exactly how to guide this synthesis to favor pure results.

    Supporting Advanced Discovery and Scale-Up

    Many inquiries start from academic groups, but as programs move to larger scale, the requirements for regulatory documentation, reproducibility, and secure logistics grow more complex. Decades producing specialty amino acids for diverse applications gave us the foundation to support both discovery-scale orders and full-scale CGMP campaigns.

    Batch traceability, real time stability monitoring, and clear documentation have become non-negotiable for any materials in preclinical or clinical use. Our continuous improvement mentality means adopting new analytical methods and responding quickly to new regulatory requirements or customer audit findings. Direct involvement in each stage gives us agility over order fulfillment and technical support—a strength missing from channels that only broker material.

    Fluorinated amino acids like 3-Fluoro-L-Tyrosine increasingly find their way into disease diagnostics and in vivo imaging. Their use moves from bench to bedside, with clinical partners adding requirements on residual solvent, heavy metals, and microbial limits. Internal experience anticipating and meeting these needs saves programs time and expense.

    Meeting Technical Demands with Experience

    Ever since we synthesized our first ten-gram sample over ten years ago, iterative improvements have become an operating principle. Our technicians document each process change and its downstream effects, building a reference archive for problem solving and rapid response. Production challenges—from coupling reagent selection to solvent recovery—reach resolution through consistent teamwork and in-house expertise.

    Customer conversations reinforce the value of these operating habits. Collaborators share synthetic headaches, instrument quirks, or application results, and our production team turns this knowledge into better workflows. Real-world stories about failed couplings, ambiguous HPLC baselines, and variable reactivity levels remind us that maintaining process discipline and detailed records isn’t just best practice—it’s essential for chemistry that works where it counts.

    Reducing Variability, Supporting Innovation

    The expansion of peptide-based research exposes how batch-to-batch variability in input reagents disrupts innovation and slows down progress. Small deviations in enantiomeric purity, particle size, or moisture level shift entire outcomes. Direct control over our supply chain—from source materials to finished packaging—means we answer only to our own performance standards, not a distant supplier’s limitations.

    Many research partners who transitioned from generic sources to our direct product line report measurable improvements. Syntheses become more reliable, and purification easier. Data emerges cleaner, with fewer outliers traced to starting material irregularities. Pharmaceutical developers especially value these gains during process validation and lot-release trials.

    Our in-depth knowledge of chemical behavior also extends to consulting on downstream processing. Whether for lyophilization, solution formulation, or solid-state delivery, our background in real-world handling conditions brings practical, actionable advice. Academic groups, fledgling biotech teams, and scale-up partners tell us that this expertise shortens development timelines, limits troubleshooting, and anchors project confidence.

    Future Directions in 3-Fluoro-L-Tyrosine Use and Manufacturing

    Growth in protein engineering, therapeutic peptide design, and biosensing technology sustains demand for ever-purer, more functionally-tuned amino acids. 3-Fluoro-L-Tyrosine promises to play a bigger role as research circles back to fundamental questions about protein dynamics and cell signaling. As experienced chemical manufacturers, we keep pace by refining synthesis routes, minimizing byproduct generation, and investing in state-of-the-art analytical platforms.

    Market developments shape our own technical targets—reducing waste solvent, improving energy efficiency, and minimizing worker exposure to hazardous materials. Implementing continuous-flow chemistry and alternative purification aids both safety and scalability. We collect feedback from researchers to adjust packaging sizes, improve labeling, and ensure reliable supply, even during global disruptions.

    Why Manufacturer Experience Matters

    Our input comes not only from routine order fulfillment, but also from years solving unexpected issues. 3-Fluoro-L-Tyrosine serves as a case study in the value of frontend experience. We handle every crystallization, melting point drift, and packaging challenge as part of a feedback-driven system. Over time these incremental corrections deliver a product that genuinely reflects what working scientists need.

    Several customers shared stories of lost research time due to reagent inconsistency from less transparent sources. Established protocols and frequent verification steps prevent these losses. Active dialogue with our customers, addressing every question from spectral impurities to solvent compatibility, builds confidence and sustained collaboration.

    Conclusion: Building Long-Term Value in Amino Acid Chemistry

    3-Fluoro-L-Tyrosine challenges easy classification. On one hand, it emerges as a vital specialty reagent for narrow segments of biochemistry and drug discovery. On the other, its impact reverberates through fundamental science, unlocks new mechanistic understanding, and reshapes protein research. As the producer, we view our role as an enabler of that progress. Every batch stands as a testament to the lessons learned on the factory floor, the conversations with working chemists, and continual adjustment in pursuit of reliability.

    Labs choosing 3-Fluoro-L-Tyrosine made through a direct manufacturing process gain the confidence to pursue critical experiments without avoidable delays. This trust does not arise by accident—it is earned through technical depth, proven results, and a steady partnership between producer and investigator. While innovations march on, some truths remain unchanged: chemistry succeeds on the foundation of skill, careful process control, and honest engagement with customers’ needs.

    With 3-Fluoro-L-Tyrosine as part of a growing portfolio, our team looks forward to supporting new breakthroughs in science and technology. Every order, every analysis, every delivery reflects a continuous commitment to quality and a shared mission to enable the discovery of tomorrow’s answers in peptide and protein research.