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6-Fluoro-DL-Tryptophan

    • Product Name 6-Fluoro-DL-Tryptophan
    • Alias 6-Fluoro-DL-TRP
    • Einecs 242-760-1
    • 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

    829731

    Product Name 6-Fluoro-DL-Tryptophan
    Cas Number 131123-71-2
    Molecular Formula C11H11FN2O2
    Molecular Weight 222.22
    Appearance White to off-white powder
    Purity Typically >98%
    Solubility Soluble in water and DMSO
    Storage Temperature 2-8°C
    Synonyms DL-6-Fluorotryptophan
    Smiles N[C@@](CC1=CNC2=CC(F)=CC=C12)(C(=O)O)
    Usage Research chemical, amino acid analog

    As an accredited 6-Fluoro-DL-Tryptophan factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 6-Fluoro-DL-Tryptophan (1g) is a sealed amber glass vial with a printed, tamper-evident chemical label.
    Shipping 6-Fluoro-DL-Tryptophan is shipped in tightly sealed, chemically-resistant containers to prevent contamination and degradation. Packaging complies with relevant regulations for hazardous laboratory chemicals. The product is transported at ambient temperature unless otherwise specified, with clear labeling and accompanying safety documentation. Expedited or temperature-controlled shipping is available upon request.
    Storage 6-Fluoro-DL-Tryptophan should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2–8°C (refrigerated). Avoid exposure to air and incompatible substances. Use appropriate personal protective equipment when handling, and ensure containers are properly labeled to prevent accidental misuse or contamination.
    Application of 6-Fluoro-DL-Tryptophan

    Applications of 6-Fluoro-DL-Tryptophan in Industrial Manufacturing

    6-Fluoro-DL-Tryptophan is a specialty amino acid derivative widely adopted across advanced industrial and research-driven sectors. As the direct manufacturer, we supply this raw material to innovators in pharmaceuticals, biochemical research, isotope labeling, and chemical synthesis who require precise compliance, customized formulation, and seamless integration into scalable industrial processes.

    1. API Synthesis for Anticancer Drug Discovery

    Pharmaceutical companies incorporate 6-Fluoro-DL-Tryptophan as an advanced building block during the synthesis of investigational APIs targeting oncology indications, particularly when fluorinated analogues are needed in SAR studies or as metabolic tracers. Our chemists support integration of this material during early-stage route development and process optimization for fluorinated tryptophan derivatives required in novel small-molecule drug candidates.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: FDA cGMP for Finished Pharmaceuticals
    • EU GMP Part II: APIs and Intermediates
    • Relevant monographs in the United States Pharmacopeia (USP) for chiral amino acids

    Typical usage ratio

    • 5–25 mol% relative to total amino acid content, with exact ratio tailored based on desired fluorination density and SAR study targets

    Downstream process integration

    • Fed as a key intermediate in solution-phase or solid-phase peptide synthesis (SPPS), or directly incorporated into multi-step routes at the coupling and cyclization stages for heterocyclic scaffold drugs

    Final product types

    • Fluorinated tryptophan-based active pharmaceutical ingredients
    • Peptide drugs with enhanced metabolic stability
    • Research drug candidates used in clinical oncology trial lots

    2. Isotope Labeling for Biomedical Research Reagents

    6-Fluoro-DL-Tryptophan provides a unique fluoroaromatic marker for isotope-labeled compounds in proteomics and metabolic pathway research. Academic and corporate laboratories utilize this material as a precursor in the synthesis of 19F-NMR or radiolabeled probes, enabling sensitive tracking of amino acid metabolism and protein turnover in complex biological samples. Close attention to purity and isotopic enrichment ensures reproducible results in quantitative omics workflows.

    Industry compliance standards

    • ISO 17034: General requirements for the competence of reference material producers
    • ISO/IEC 17025: General requirements for the competence of testing and calibration laboratories
    • IUPAC guidelines for stable isotope labeling

    Typical usage ratio

    • Typically 0.5–5 mmol/L in labeling reaction mixtures, based on tracer incorporation level and sensitivity required for analytical quantification

    Downstream process integration

    • Introduced during the chemical or enzymatic synthesis of labeled peptides and proteins, as well as in cell culture feeding for in vivo tracer studies

    Final product types

    • 19F-labeled amino acid standards for metabolomics
    • Isotope-enriched proteins for NMR structural analysis
    • Synthetic peptides with site-specific fluorination

    3. Precursor for Custom Peptide Synthesis in Proteome Engineering

    Peptide synthesis companies and contract research organizations select 6-Fluoro-DL-Tryptophan to produce specialized peptide sequences with altered spectral, metabolic, or immunogenic properties. Its use enables development of diagnostic peptide reagents, neoepitope vaccines, and affinity capture ligands where site-directed fluorination modulates stability or analytical detection. Our production adheres to strict quality protocols, allowing for scale-up and consistent supply in complex multi-residue custom syntheses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for peptide manufacturers
    • Synthetic peptide quality standards outlined by the American Peptide Society
    • Chemical import/export documentation per relevant jurisdiction for custom synthesis

    Typical usage ratio

    • Single-site incorporation at 1 mol % per sequence when replacing native tryptophan, or up to 10 mol % for multi-site modifications in diagnostic or screening reagents

    Downstream process integration

    • Coupled at designated codons during automated SPPS, often as a protected Fmoc or Boc derivative for on-resin insertion, ensuring precise localization of fluorine groups

    Final product types

    • Synthetic peptides for analytical standardization
    • Neoantigen-based vaccine constructs
    • Fluorescently taggable bioaffinity ligands

    4. Fine Chemical Intermediate for Agrochemical R&D

    R&D divisions within agrochemical companies leverage 6-Fluoro-DL-Tryptophan as a niche intermediate when developing crop protection molecules inspired by indole alkaloid biosynthesis patterns. Fluorinated tryptophan analogues support the rapid synthesis of candidate molecules aimed at improved insecticidal or fungicidal properties. Control over chirality and substitution positioning increases the diversity of chemical libraries for agricultural biochemistry screens.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical research
    • Chemical hazard labeling and transportation as defined by GHS and REACH (EU)
    • ISO 14001 Environmental Management Systems for sustainable R&D

    Typical usage ratio

    • 2–15 mol% within reaction mixtures, with doses adjusted during lead optimization to achieve desired substitution and molecular diversity in combinatorial synthesis

    Downstream process integration

    • Incorporated during the multi-step synthesis of indole-derived core structures, serving as a fluorinated precursor in condensation, halogen exchange, or functionalization reactions

    Final product types

    • Lead analogues for agrochemical library screening
    • Prototype bioactive indole alkaloids for field evaluation
    • Early-stage fungicide/insecticide testing batches
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    Competitive 6-Fluoro-DL-Tryptophan prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    6-Fluoro-DL-Tryptophan: Expertise and Insights from the Production Floor

    Understanding the Product and Its Place in Chemistry

    6-Fluoro-DL-Tryptophan stands out in the world of synthetic amino acids. In our work as a chemical manufacturer, the process of introducing a fluorine atom to the aromatic ring of the tryptophan structure creates new possibilities in research and product development. The significance of this modification goes beyond a simple atomic substitution—it changes the electronic nature of the molecule, influences its interactions with enzymes and receptors, and opens up distinct biochemical pathways unavailable to traditional tryptophan.

    Production Methods and Material Control

    In our manufacturing line, the production of 6-Fluoro-DL-Tryptophan follows routes designed for accuracy and reproducibility. Careful selection of precursor materials, close attention to reaction conditions, and rigorous purification steps are not just matters of protocol—they form the backbone of our responsibility toward customers who rely on our products for research, pharmaceutical discovery, and other advanced applications. Batch-to-batch consistency relies on precise fluorination methods and chromatographic separation, and we invest daily in quality oversight rather than relying on occasional spot checks.

    Specifications and Typical Physical Properties

    Talking about the product itself, 6-Fluoro-DL-Tryptophan appears as a white to off-white solid under ordinary conditions. Tested under strict QC protocols, the purity regularly reaches levels above 98%. Moisture levels, residual solvents, and trace inorganic impurities remain tightly controlled. Particle size and flow characteristics matter in our daily work as these affect both the handling on the production line and downstream processing for customers. Our technicians run HPLC, NMR, and MS analyses—not as afterthoughts, but as main tools for verification.

    Reasons for Using the DL Form

    The choice of DL configuration is deliberate and comes with practical advantages. Racemic mixtures provide an even-handed starting point for studies where stereochemistry may influence biological outcomes, but the initial requirement is often screening, not fine discrimination between enantiomers. Researchers use the DL form for preliminary assays and identification of enantiospecific activity before investing resources in resolving or synthesizing the pure optical isomers. Supplying the DL mixture supports a wide scope of inquiries, especially in the early phases of drug development.

    Interacting with Biological and Pharmaceutical Research

    6-Fluoro-DL-Tryptophan enters the pipeline of many research projects in biochemistry, enzyme engineering, and neuropharmacology. Substitution with fluorine can disrupt natural metabolic pathways, serving both as a tracer in biochemical assays and as a tool for probing protein-ligand interactions. Fluorinated analogs show altered binding properties in target enzymes, affecting catalysis and offering a platform for the creation of mechanism-based inhibitors or modified peptide drugs.

    Because fluorine introduces both size and electronegativity changes at a specific position, our customers report sharper signals in NMR studies and stronger resistance to metabolic degradation compared to unmodified tryptophan. These two features address two common challenges: detection sensitivity and molecule stability in vivo and in vitro. For instance, medicinal chemists swapping the indole hydrogen for a fluorine report slowed oxidative breakdown—valuable for extending pharmacokinetic lifetimes or fine-tuning lead compounds.

    Comparison with Non-Fluorinated and Other Substituted Tryptophans

    From a manufacturer’s lens, differences between 6-Fluoro-DL-Tryptophan and natural tryptophan or its other analogs stem from more than added production steps. A standard amino acid such as L-tryptophan integrates easily into proteins and metabolic cycles, but the introduction of a halogen changes this profile significantly. Where standard tryptophan metabolizes via established pathways, fluorinated forms demonstrate reduced catabolism, altered transporter affinity, and sometimes bypass traditional feedback regulation within cells. These differences shape their utility in mechanistic studies and as tool compounds in cell culture or animal models.

    Customers sometimes ask whether to choose other substituted tryptophans—for example, 5-fluoro or 7-fluoro variants. Our long-term observation is that the ring position of the substitution changes the electron density and hydrogen bonding pattern, so binding to enzymes or receptors follows unique trends. The 6-position provides a balance between substantial modification and retention of side-chain integrity, which is evident in its continued popularity across research publications. Additionally, the 6-fluoro variant shows greater synthetic accessibility and sustainability at industrial scale than some less common positional isomers, which can run into low yields or expensive separation challenges.

    Applications in Labeling, Assays, and Synthesis

    6-Fluoro-DL-Tryptophan finds heavy use in the field of chemical biology as a labeling agent. The presence of fluorine provides an unmistakable handle for 19F NMR studies. Researchers tracking protein folding, ligand interactions, and signal transduction have found this molecule useful for inserting a distinct NMR signature without introducing bulky groups that could disrupt biomolecular function. The balance of minimal steric hindrance and spectral visibility makes it a favored probe.

    Beyond NMR, the unique reactivity of the fluorinated indole is valuable in synthetic chemistry for building new compounds. Medicinal chemists apply this molecule as a building block for peptidomimetics and non-natural polymers, benefiting from both its stability and unique reactivity profile. Radiolabeling with 18F atoms, though technically distinct from our product, traces its roots to the availability and reactivity of precursors such as 6-fluoro tryptophan. In this sense, our expertise as a producer feeds into much larger efforts toward imaging agents and diagnostic tracers.

    Focus on Purity, Traceability, and Batch Consistency

    Customers operating under tight regulatory oversight and in high-stakes research settings expect clear and consistent answers about product specifications. We don’t see quality control as a set of checkboxes, but as a shared foundation for scientific progress. Detailed batch records, calibration logs, and retention samples demonstrate not just compliance, but confidence in every gram leaving our facility.

    We continually monitor feedback from users about product performance. Occasionally, end users have observed unexpected peaks in mass spectra or slight impurities in highly sensitive applications. Every customer report triggers a review—inspection of process reagents, review of analytical data, and thorough tracking of production variables. Our on-the-ground adjustments have led to improvements in reaction quenching and refinement of chromatographic separations. By focusing not just on end-product numbers but on upstream process control, we maintain a high bar for reproducibility on every lot, learning along the way from each new application or user feedback.

    Sustainability and Responsible Manufacturing

    As the market for modified amino acids grows, expectations for environmental stewardship climb alongside. The synthetization of halogenated organics carries both energy and waste burdens. Our team continually revisits process chemistry to minimize hazardous solvents and optimize reactions for maximum conversion. The shift toward greener synthesis—in both choice of reagents and process engineering—reflects not only regulatory trends but our own values shaped by years on the factory floor. Recovered solvents, contained side streams, and solvent recycling see daily use rather than remaining lofty goals on safety audits.

    Our waste minimization efforts focus primarily on reaction yield improvement and solvent recovery protocols. We run periodic reviews of all raw materials, track real-world data on re-use cycles, and conduct lifecycle analyses on product streams. These practices arise from necessity as much as philosophy: reducing waste and optimizing efficiency secure cost stability for both our operation and our customers’ budgets.

    Meeting Researcher Demands and Responding to Innovation

    We’ve witnessed the research landscape shift toward rigorous, data-driven protocols over the past decade. As peer review intensifies and reproducibility draws more scrutiny, the integrity of starting materials gains more weight. Our commitment rests not only on making the product available, but on making it trustworthy. Transparency in sourcing, validation in analytical data, and responsiveness to user concerns have, over time, defined our reputation.

    Requests for custom batch sizes, specialized purity levels, and documentation traceable to regulatory standards now arrive far more frequently. We support custom synthesis when necessary, but always stress the importance of full technical disclosure. As a manufacturer, we welcome dialogues with end users—our chemists regularly collaborate with clients to address application-specific challenges, ensuring compatibility between our process and their experimental design. This approach requires more investment up front, but delivers clarity and trust that support advancement and avoid downstream risk.

    Limitations and Challenges in Supply and Use

    Commercial production of 6-Fluoro-DL-Tryptophan encounters periodic challenges familiar to any industrial chemist. Raw material shortages, fluctuation in demand, and evolving regulations affect both availability and cost structure. Supply chain resilience demands a diversified slate of suppliers for precursor materials, buffer stocks, and investment in long-term raw material contracts. External shocks—such as supply interruptions or regulatory changes on key reagents—require us to act nimbly to maintain commitments.

    In practical use, customers sometimes report sensitivity to light or moisture over extended storage. We advise both our staff and users on best practices for handling and storage, favoring amber packaging and low-humidity warehouse facilities. From packaging design down to pallet-level logistics, small details matter: too much exposure to atmospheric moisture can cause caking or slow degradation, both of which impact the usability in sensitive biological or analytical applications.

    Solutions and Forward-Looking Development

    Long-term investment in R&D functions as our safeguard against both supply disruptions and manufacturing inefficiencies. Our chemists explore alternative synthetic routes, either for greater economies of scale or for gentler environmental footprints. Continuous process improvement comes from both in-house initiative and from end-user collaboration. For instance, a new continuous flow process under study in our facility aims to reduce batch turnaround time and cut down on solvent consumption by up to one third.

    In direct response to customer feedback, we have adopted advanced packaging solutions to prolong shelf life. Vacuum-sealed and inert atmosphere pouches now form part of our standard offerings, and we periodically validate packaging integrity through real-time and accelerated stability studies. By tuning both the chemical and logistical arms of our business, we keep a keen eye on product performance from synthesis to final use.

    Innovation cannot ignore the demand for tighter chiral control. Enantioselective synthesis and advanced separation techniques form active areas of investigation in our laboratories. We maintain dialogue with researchers driven to explore enantiopure 6-fluoro-tryptophan’s pharmacological potential, recognizing that robust supply of both racemic and single-isomer products, with traceable quality data, will drive the next wave of biomedical advancements.

    Summary of Unique Manufacturer Perspective

    As direct producers of 6-Fluoro-DL-Tryptophan, we recognize responsibility goes far beyond fulfilling orders. From raw material procurement to final delivery, every decision reflects decades of accumulated technical expertise and ongoing commitment to the scientific community. Our daily work ties us to advances in chemical biology, diagnostics, and pharmaceutical innovation—fields that rely on absolute confidence in the building blocks we provide. We continue learning from our production floors, customer partnerships, and the relentless pace of chemical innovation. Through steady investment in quality, transparency, sustainability, and technical support, we build a foundation not only for reliable supply, but for the trust that underpins long-term scientific progress.