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L-Leucyl-L-Tyrosine

    • Product Name L-Leucyl-L-Tyrosine
    • Alias Leu-Tyr
    • Einecs 256-803-4
    • 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

    239031

    Chemical Name L-Leucyl-L-Tyrosine
    Cas Number 3452-55-9
    Molecular Formula C18H24N2O4
    Molecular Weight 332.4 g/mol
    Appearance White to off-white powder
    Solubility Slightly soluble in water
    Melting Point Approximately 255°C (decomposes)
    Iupac Name (2S)-2-[(2S)-2-amino-4-methylpentanamido]-3-(4-hydroxyphenyl)propanoic acid
    Storage Conditions Store at 2-8°C, dry place
    Usage Used in biochemical research and peptide synthesis

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

    Packing & Storage
    Packing Amber glass bottle, white screw cap, labeled "L-Leucyl-L-Tyrosine," 5g, purity >98%, chemical safety symbols, and batch/expiry details.
    Shipping L-Leucyl-L-Tyrosine is shipped in sealed, airtight containers to ensure product stability and prevent contamination. It is typically packaged in amber bottles or high-integrity plastic vials, cushioned for safe transit. Shipping follows relevant regulations for non-hazardous chemical substances, avoiding extreme temperatures and humidity to maintain chemical integrity throughout transport.
    Storage L-Leucyl-L-Tyrosine should be stored in a tightly sealed container, protected from light and moisture. Keep the chemical at 2–8°C (refrigerated) and in a well-ventilated, dry place. Avoid exposure to heat or strong oxidizing agents. Proper labeling and secure storage are essential for safety and maintaining the compound’s stability and purity.
    Application of L-Leucyl-L-Tyrosine

    Applications of L-Leucyl-L-Tyrosine in Industrial Manufacturing

    L-Leucyl-L-Tyrosine, as a dipeptide intermediate, serves critical roles across several specialty manufacturing sectors. Our facilities produce this raw material with strict attention to downstream customer requirements, particularly where traceability, purity, and regulatory standards drive batch acceptance. Below, we detail the principal industrial applications based on real world manufacturing use, supported by industry standards and our own production expertise.

    1. Peptide Drug Synthesis for Pharmaceutical APIs

    Pharmaceutical manufacturers use L-Leucyl-L-Tyrosine as a protected dipeptide building block in solid-phase peptide synthesis (SPPS) and solution-phase peptide synthesis lines. This intermediate feeds directly into multi-step API assembly, supporting both small-molecule peptide generics and research-stage bioactive compound development. High-purity requirements and trace-level by-product controls are essential due to strict health authority reviews at both the intermediate and final API stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monographs (where applicable for peptide intermediates)
    • FDA 21 CFR Part 210/211 (for US GMP)
    • EDQM/Ph. Eur. standards for peptide APIs

    Typical usage ratio

    • 0.5–1.5 molar equivalents per desired peptide coupling step, adjusted based on sequence length and coupling efficiency targets

    Downstream process integration

    • Direct charging into resin vessels for SPPS cycles following Fmoc deprotection
    • Solution addition during stepwise solution-phase peptide synthesis amidations
    • Purified and QC-tested dipeptide introduced prior to main chain elongation

    Final product types

    • Hospital-formulated peptide drug APIs (e.g., injectable polypeptides, analogues of hormone peptides)
    • Research-grade synthetic peptides
    • GMP-compliant intermediates for further peptide chain extension

    2. Nutritional Supplementation Premix Manufacturing

    Specialty nutrition manufacturers incorporate this dipeptide into amino acid premixes for clinical nutrition, enteral feeding formulations, and performance nutrition blends. L-Leucyl-L-Tyrosine offers enhanced bioavailability in comparison to free amino acids, allowing formulation scientists to standardize nitrogen content while controlling taste and solubility across various powder and liquid premix systems destined for professional dietetic products.

    Industry compliance standards

    • Codex Alimentarius standards for protein and amino acid supplements
    • FDA 21 CFR Part 111 (Dietary Supplement cGMPs, US)
    • EU Regulation (EC) No 1925/2006 (Addition of Nutrients to Foods)
    • GB 14880 Food Additive Use Standard (China, relevant for dairy/nutrition export blends)

    Typical usage ratio

    • 0.1–1.0% w/w in amino acid blends; actual inclusion rate decided by dietary protein equivalence and intended application (e.g., clinical, sports nutrition, or functional food fortification)

    Downstream process integration

    • Blending with other essential and branched-chain amino acids during spray drying of powder premixes
    • Wet granulation added before tableting for custom dietary supplements
    • Direct tank mixing for ready-to-drink nutritionals post-sterilization step

    Final product types

    • Pediatric and adult clinical nutrition powders
    • Enteral tube feeding solutions
    • Performance and fitness amino acid premixes
    • Customized functional food ingredient blends

    3. Cell Culture Media and Bioprocessing Components

    Bioprocess developers, especially those scaling mammalian and microbial cell cultures for biologics manufacturing, require highly defined dipeptides as part of cell culture media optimization. L-Leucyl-L-Tyrosine minimizes precipitation and improves tyrosine delivery to rapidly growing cells, supporting reproducibility, higher yields, and robust downstream protein expression, particularly in serum-free and chemically defined media systems.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (for cell media manufacturing)
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • EMA Guidance on Raw Materials Used in the Manufacture of Biologics
    • ICH Q5A/B (Viral Safety and Cell Substrate Guidance)

    Typical usage ratio

    • 0.05–0.3 g/L in basal and feed media, dependent on cell line and culture system requirements; ratio optimized for tyrosine bioavailability without inducing precipitation

    Downstream process integration

    • Dissolved directly into basal media or post-autoclave feeds under sterile filtration
    • Combined in-house with other dipeptide sources during high-density fed-batch preparations
    • Added as a specific tyrosine source for recombinant protein production runs

    Final product types

    • Animal cell culture media powders and liquids
    • Microbial fermentation process media (e.g., E. coli, yeast systems)
    • Bulk bioreactor feed additives for monoclonal antibody production
    • Custom feeds for vaccine and therapeutic protein manufacturing

    4. Diagnostic and Research Reagent Production

    Producers of specialized diagnostic kits and peptide reference standards employ L-Leucyl-L-Tyrosine as a calibration compound, enzyme substrate, or synthetic peptide control. Its well-defined structure supports high-precision quantitative assays and serves as a functional validation component in method development for chromatography and immunoassay workflows. Quality requirements hinge on batch consistency, trace impurity profiling, and lot-to-lot reproducibility for regulated laboratory supply chains.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management for IVDs
    • CLSI Guidelines (Clinical & Laboratory Standards Institute)
    • OECD GLP Principles for Laboratory Testing
    • FDA Quality System Regulation 21 CFR Part 820 (for US medical devices, diagnostics)

    Typical usage ratio

    • 5–50 µg/mL as a calibration standard in analytical workflows
    • 0.02–0.2% w/w in peptide substrate formulations, depending on assay sensitivity and detection requirements

    Downstream process integration

    • Dispensed into freeze-dried calibration kit vials
    • Solution blending for enzyme kinetic assays or HPLC standard curves
    • Solid phase conjugation during functionalization of microplate assays

    Final product types

    • In vitro diagnostic calibration kits
    • Peptide substrate standards for laboratory analysis
    • Quality control reference peptides for chromatography and ELISA
    • Enzyme-linked immunosorbent assay components
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    Certification & Compliance
    More Introduction

    Introducing L-Leucyl-L-Tyrosine: Our Perspective as the Maker

    The Value Behind L-Leucyl-L-Tyrosine

    Every batch of L-Leucyl-L-Tyrosine carries the mark of our facility, not just because we synthesize and purify every gram on-site, but because we recognize its value goes beyond a standard peptide. After years in amino acid manufacturing, we watch market trends fluctuate as applications change for health, research, cosmetics, and even food science. Still, this dipeptide stands out for anyone seeking more than just bulk raw material.

    L-Leucyl-L-Tyrosine, often called Leu-Tyr, comes from joining two well-known amino acids: leucine and tyrosine. Our chemists combine the two through controlled peptide synthesis, yielding a white to off-white powder, clean in appearance, with a characteristic sequence that keeps its integrity through storage and shipping. The model code that our customers refer to in orders identifies specification parameters such as purity, molecular formula (C15H22N2O3), and batch information. Every time we take a sample for HPLC assay, we’re reminded that the 98% or higher purity target isn’t just marketing—it’s our wheelhouse.

    Where Real-World Change Starts: Applications and Real Needs

    We have watched the use of peptide-based compounds grow in precision applications. Researchers in protein metabolism gravitate toward simple peptides like L-Leucyl-L-Tyrosine because their sequence allows for easy mapping in enzymatic breakdown studies. There’s a practicality here: the simplicity of dipeptides cuts down on ambiguity, making it easy to isolate specific activity during enzyme kinetics, absorption, and even transport studies.

    Nutritional research labs order our L-Leucyl-L-Tyrosine to examine how short-chain peptides move across intestinal walls. Because the body recognizes this dipeptide as a nutrient load distinct from free amino acids, it shows faster absorption and lower competition at certain transporters. Formulators in medical nutrition and advanced supplementation see the point—sometimes, a dipeptide enables the targeted delivery of amino acids without the strong taste or reactivity of the single components.

    Cosmetic scientists working on skin and hair applications have contacted our technical support, asking for lots with tight control over heavy metals and residual solvents. The peptide proves useful in these spaces because the leucine-tyrosine link brings together the hydrophobic properties of leucine with the aromatic, hydrophilic character of tyrosine, giving the blend a unique solubility—good for topical delivery systems.

    The global discussion around protein hydrolysates and bioactive peptides also covers peptides like L-Leucyl-L-Tyrosine. Functional food producers aiming to achieve specific protein profiles in hydrolysates order it to use as a calibration standard, or even as a model compound for designing protein digestibility trials in their pilot plants. Our experience shows that these practical, hands-on uses are too specific for generic amino acid blends to fulfill.

    Specification and Batch Consistency—Why It Matters

    Purity in this context means more than meeting a spec sheet. Impurities in a dipeptide may cause problems—cross-peaks in chromatography, batch-to-batch flavor differences, or even failed biological assays. We don’t just chase numbers; we test for trace elements and peptide-related impurities, making sure that our L-Leucyl-L-Tyrosine doesn’t disrupt complex research protocols.

    The crystalline powder we produce resists caking and stays free-flowing, which helps both high-throughput screening labs and artisan protein formulators. We package according to customer usage patterns, whether they call for small technical samples or multi-kilogram compounding sacks. Our own stability tests verify shelf life above two years, storing at room temperature, away from sunlight and moisture.

    End users sometimes worry about excipients or stabilizing agents. Our approach has always been to avoid them unless the customer specifically asks for a blend. The dipeptide is free from fillers and carriers—every analytical result we offer stands for the compound itself, not an adjunct or processing aid.

    What Distinguishes L-Leucyl-L-Tyrosine from Other Amino Acid Products

    Peptide chemistry is a world apart from single amino acid manufacturing. Free amino acids like leucine or tyrosine exist as basic building blocks. When we form L-Leucyl-L-Tyrosine, two molecules combine through an amide bond, creating new chemical behavior. This isn’t just about stringing beads on a necklace. The dipeptide backbone gives the compound new properties. For example, it becomes less susceptible to rapid breakdown by single-enzyme systems, making it useful in controlled-release or absorption models. The bitterness profile changes too, which affects food and drink applications that demand a more neutral flavor.

    If you put side-by-side samples of L-Leucyl-L-Tyrosine and free leucine, you’ll notice that their moisture absorption patterns differ. This matters for powder stability, flow rates through processing equipment, and even suitability for tableting or encapsulation. Tyrosine, on its own, resists dissolution; its crystalline nature requires fine milling. The dipeptide form offers quicker solubility both in water-based and some organic matrices, which expands its range of compatible formulations.

    Our process builds out the product to its full analytical fingerprint—second N-terminal position, free carboxyl end, intact amide linkage. These details affect how the dipeptide interacts in enzymatic hydrolysis and how it behaves in metabolic studies. In peptide science, the story often lies in the sequence. Our facility maintains strict control over side-chain protection and removal, guaranteeing there’s no racemization, so users know what’s in their beaker is authentic L-form dipeptide.

    Quality Control and Analytical Validation—Our Real-World Approach

    Maintaining consistent quality starts before synthesis. We keep a strict record of incoming raw material—our starting leucine and tyrosine both exceed 99% purity, and each batch passes identification protocols involving NMR and mass spectrometry. The peptide coupling process runs under anhydrous conditions, bypassing the most common causes of byproduct formation. Our analytical chemists validate finished lots through HPLC, not just for the main peak, but for trace contaminants, including D-form analogs and potential decomposed residues.

    In practice, our technical staff test for solubility, pH of 1% solutions, and microbiological contamination. Questions from customers about allergen status, non-animal origin, and trace solvents get answered from a supply chain we oversee in-house. This control means researchers and formulators don’t have to make guesses—what they order matches the certificate of analysis on file, every order, every lot.

    Temperature and humidity stability gets checked through real cycling; we stress test samples in conditions far outside those typically found in storage rooms just to guarantee performance even in tough shipping cycles worldwide. Customers in regions with high humidity see the benefit—clumping and hydrolysis-related off-smells never enter the conversation.

    Who Uses L-Leucyl-L-Tyrosine and What They’re Solving

    University biochemistry labs often apply L-Leucyl-L-Tyrosine as a model substrate for studying peptide transporters and protease specificity. We supply grant-driven projects needing reproducible substrates for uptake kinetics in cell lines and tissue preparations. Our facility receives requisitions from clinical nutrition developers seeking pharmaceutical-grade peptides to investigate rare metabolic disorders in pediatric nutrition—they require consistent, defined sources where batch drift won’t compromise a multi-year study.

    Some protein supplement companies ask for dipeptides to meet demand for advanced BCAA blends, others want to eliminate the bitter aftertaste that single amino acids sometimes cause. In sports nutrition, those looking for rapid recovery formulas find that dipeptides bypass simpler amino acid competition at gut transport sites, potentially speeding up delivery to muscle tissue. Our data comes back from product developers trying to reduce powder aftertaste and improve mixability in ready-to-drink beverages.

    Biotechnology companies order kilograms for peptide mapping standards or as building blocks for longer synthetic peptides. Their QC teams care about consistent chain integrity, which our synthesis and purification lines are set up to deliver. We get questions about sequencing accuracy; our in-house MALDI-TOF and amino acid analysis assure them that the L-Leucyl-L-Tyrosine supplied matches sequence-limited reference spectra.

    Cosmetic and personal care groups explore the dipeptide for topical applications, seeing benefits in gentle delivery and compatibility with hydrogel and emulsion systems. They want assurances on residue levels and stability under UV exposure, requirements our R&D tests mirror every quarter.

    Challenges We Tackle in Manufacturing and Use

    Sourcing genuine, non-contaminated starting materials runs at the core of dependable peptide manufacturing. Over the years, we’ve countered offers of low-grade inputs that undercut real value—striking those from our supply list keeps contamination out of customer formulations. We’ve learned that some types of surface glass can catalyze trace breakdown under storage, so we package only in certified, tested containers.

    Our synthesis lines focus on eliminating racemization, a challenge when coupling hydrophobic residues like leucine. The result is a lot-to-lot reproducibility that synthetic chemists appreciate when scaling up processes or validating high-throughput screens. Hydrolysis risk increases with moisture, so every production run faces monitoring for residual solvents, and we use vacuum drying protocols developed in our own labs.

    Shipping peptides can create headaches if not handled carefully; we address this by controlling every element, including secondary containment, to insulate from fluctuations in cargo areas. Our customer support logs show that product failures often trace back to exposure outside recommended storage—even with our packaging, we encourage users to maintain low-humidity, sealed storage to extend shelf life and guarantee analytical consistency.

    Future Directions and Customer Feedback—The Driving Force

    One thing we don’t overlook is how feedback steers our approach. Product managers from clinical nutrition and sports supplement brands challenge us for new specification targets—higher purity, lower microbial counts, or stricter allergen screening. Our development team, in turn, responds by adapting synthetic and purification methods, training staff on emerging regulatory requirements, and maintaining up-to-date analytical protocols.

    We receive requests from peptide therapeutics manufacturers who want to move from milligram to kilogram scale; scaling up without losing integrity keeps our process engineers busy, ensuring no batch deviates from the qualification results advertised. Research scientists mention that dependable dipeptides allow for better reproducibility, which in academic publishing means fewer variable results.

    Technology doesn’t stand still here. We keep investing in better synthesizers, upgrading to higher-efficiency mixers and column chromatography, and updating our reference standards as new pharmacopeia listings get released. We listen closely when lab directors talk about failed shipments caused by old packaging designs—our packaging methods change to match user input, and our technical sheets draw from ongoing field experience, not just regulatory tables.

    Peptide customization is becoming more common as end users pursue next-level formulations for targeted outcomes. For customers aiming for specific bioactive profiles or unusual solubility targets, we offer tailored production runs. It’s no longer enough to make a dipeptide to standard spec—users expect the ability to request their own purity targets, packaging sizes, and supplementary analytical tests.

    Comparison with Other Offered Peptides

    L-Leucyl-L-Tyrosine holds a unique place within our peptide catalog. While products like L-Alanyl-L-Glutamine or Glycyl-L-Leucine address different branch points in research and formulation, Leu-Tyr offers a blend of bulk hydrophobic character and aromatic activity. Unlike shorter peptides, it delivers more resistance to breakdown, improving shelf stability in commercial and research settings. Compared to longer oligomers, it remains manageable for most labs, inexpensive to characterize, and easy to dissolve without specialized protocols.

    Some customers compare dipeptides like L-Leucyl-L-Tyrosine to protein hydrolysates or peptide blends from non-synthetic sources. The difference becomes clear in analytical purity, batch definition, and functional predictability. Enzymatic hydrolysates may contain dozens of low-level fragments and untraceable modifications; what we provide comes as a uniform, well-defined compound, which supports transparent research and consistent blending in functional products.

    Commitment to Sustainability and Transparency

    Materials sourcing continues to evolve. Pressure for non-animal origin, sustainable, and regionally traceable raw materials runs strong across our customer base. We have restructured our procurement to prioritize plant-sourced amino acids, issued traceability documentation, and worked with supply chain agents to cut down the carbon footprint of transportation and packaging. Users increasingly ask how our peptides fit into broader sustainability initiatives, and our answer leans on real certification—no greenwashing, just transparent trace-back.

    Our internal process ensures every shipment leaves with clear documentation and up-to-date analytical data. We believe that users, especially those developing finished consumer products, deserve open conversation about origin, purity, manufacturing standards, and application.

    Conclusion: L-Leucyl-L-Tyrosine’s Place in Advanced Chemistry and Production

    Years of manufacturing L-Leucyl-L-Tyrosine have taught us that the story of one compound touches every stage of chemical technology—from fundamental research through market-ready products. It’s no longer just an ingredient; it’s a tool for unlocking insights across science, nutrition, and health. We find meaning in every kilogram produced, and every inquiry from users pushes us to refine our process, listen, and improve.

    Those using L-Leucyl-L-Tyrosine see its value in clarity and dependability, supported by a production philosophy rooted in understanding chemical behavior, practical application, and transparent service. Through decades in peptide manufacturing, we see this compound not just as a product, but as a bridge between our expertise and the needs of the world’s leading innovators.