Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

D-Leucyl-L-Tyrosine

    • Product Name D-Leucyl-L-Tyrosine
    • Alias L-Leucyl-L-tyrosine
    • Einecs 259-983-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    503016

    Chemical Name D-Leucyl-L-Tyrosine
    Molecular Formula C15H22N2O4
    Molecular Weight 294.35 g/mol
    Cas Number 19347-66-5
    Appearance White to off-white powder
    Solubility Soluble in water
    Structure Type Dipeptide
    Smiles CC(C)CC[C@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)N)C(=O)O
    Chirality D-Leucine and L-Tyrosine residues
    Iupac Name (2S)-2-(2-amino-4-methylpentanamido)-3-(4-hydroxyphenyl)propanoic acid
    Storage Temperature 2-8°C
    Usage Research and biochemical applications

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

    Packing & Storage
    Packing D-Leucyl-L-Tyrosine is supplied in a 1g amber glass vial, sealed, labeled with product details, batch number, and safety information.
    Shipping D-Leucyl-L-Tyrosine is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically packaged in accordance with regulatory guidelines for non-hazardous chemicals, using cushioning materials to ensure stability during transit. Store and transport at room temperature away from direct sunlight and incompatible substances.
    Storage D-Leucyl-L-Tyrosine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and stored at 2-8°C (refrigerated) to maintain stability. Avoid exposure to excessive heat or incompatible substances. Use appropriate personal protective equipment when handling and ensure storage is clearly labeled and compliant with safety regulations.
    Application of D-Leucyl-L-Tyrosine

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

    D-Leucyl-L-Tyrosine serves as a specialized raw material with critical applications across high-value-added life sciences industries. As a manufacturer, we supply this dipeptide to clients integrating the material into regulated bioprocesses, advanced pharmaceutical synthesis, clinical diagnostic platforms, functional nutrition, and industrial peptide chemistry. Every segment requires strict compliance, accurate formulation, validated downstream processing, and produces distinct end-use products aligned with market regulations and technical standards.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Peptide Drugs

    Biopharmaceutical companies use D-Leucyl-L-Tyrosine as an essential intermediate during the stepwise solid-phase peptide synthesis (SPPS) of certain peptide-based APIs. This material supports chain elongation and sequence-specific incorporation in molecule assembly processes that demand chirally pure and high-purity inputs to meet current industry and regulatory requirements for injectable and oral peptide drugs targeting metabolic, neurological, or endocrine indications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <1045> Peptide Mapping and Characterization
    • European Pharmacopoeia (Ph. Eur.) quality monographs for peptide substances
    • FDA cGMP regulations for pharmaceuticals (21 CFR Part 210/211)

    Typical usage ratio

    • 1–5 mol% per respective dipeptide block during full-length peptide assembly.
    • Exact input ratio based on peptide sequence design and target yield, with adjustments for protecting group strategy.

    Downstream process integration

    • In-line addition on resin-bound chain during automated or manual SPPS cycles.
    • Chemical coupling following Fmoc/Boc deprotection steps, with subsequent cleavage/purification procedures.
    • QC of coupled dipeptide established by HPLC and MS during synthesis validation.

    Final product types

    • Peptide hormone APIs
    • Antidiabetic peptide drugs
    • Peptide analogs for oncology and rare diseases
    • Custom research-grade peptides for clinical trials

    2. Diagnostic Peptide Substrate Manufacturing

    Clinical diagnostic kit producers incorporate D-Leucyl-L-Tyrosine into enzyme substrate formulations for in-vitro assays. The dipeptide serves as a selective substrate for enzymatic action (e.g., protease activity detection) in immunoassays and biochemical screening kits. Manufacturers demand consistent lot-to-lot chemical stability, strict traceability, and documented analytical validation for medical device submissions and batch release.

    Industry compliance standards

    • ISO 13485 Medical Devices Quality Management Systems
    • FDA 21 CFR Part 820 (Quality System Regulation for Medical Devices)
    • CLSI EP05 Evaluation Protocols for Precision of Quantitative Measurement
    • EU In Vitro Diagnostic Medical Devices Regulation (IVDR) 2017/746

    Typical usage ratio

    • 0.01–0.5 mg/mL in aqueous buffer for in-vitro diagnostic formulation.
    • Ratio adjusted by target enzyme kinetics and assay sensitivity requirements.

    Downstream process integration

    • Solubilization and filtration into diagnostic kit reagent mixtures.
    • Sterile filling and aliquoting into vialed substrate components or lyophilized kit packs.
    • In-process validation by spectrophotometric and enzymatic activity assay.

    Final product types

    • Protease activity detection assay kits
    • High-throughput screening substrates for automated platforms
    • Chromogenic or fluorogenic peptide substrate vials
    • Clinical pathology test panels

    3. Nutritional Peptide Ingredient for Functional Foods

    Food ingredient manufacturers formulate D-Leucyl-L-Tyrosine into functional protein hydrolysates and nutritional blends utilized in specialized health foods and supplements. The dipeptide provides a source of branched-chain and aromatic amino acids in hydrolysate matrices, targeting enhanced amino acid balance and bioavailability for sports nutrition or medical diets. Documentation focuses on global food safety and additive registration, validated amino acid profiling, and substantiated input levels for end-use claims.

    Industry compliance standards

    • Food Chemicals Codex (FCC) standards for amino acid and peptide additives
    • EU Regulation (EC) No 1333/2008 on Food Additives
    • ISO 22000 Food Safety Management Systems Certification
    • Generally Recognized As Safe (GRAS) self-affirmed dossiers (USA)

    Typical usage ratio

    • 0.05–1.0% w/w in protein hydrolysate or finished formula, adjusted by target nutritional profile and local regulatory maximums.

    Downstream process integration

    • Batch mixing with other peptide/amino acid sources before spray drying or granulation.
    • Blending into ready-to-drink or powdered formulas under food GMP controls.
    • Nutritional composition verified during QA release testing by amino acid analyzer.

    Final product types

    • Sports nutrition amino acid supplements
    • Medical food oral supplements
    • Protein hydrolysate-enriched beverages
    • Infant medical nutrition powder

    4. Chemical Building Block for Custom Peptide Synthesis Services

    Contract peptide synthesis providers and peptide CROs use D-Leucyl-L-Tyrosine as a building block for rapid made-to-order peptide sequence assembly. Clients in research, preclinical, and early-phase development specify this dipeptide for targeted sequence inclusion, demanding high chemical purity, lot documentation, and traceable synthetic origin to enable structure-activity studies and SAR campaigns.

    Industry compliance standards

    • ISO 9001 Quality Management System for chemical synthesis services
    • Certificate of Analysis (COA) with traceability to internal batch and QC
    • Material transfer and chain-of-custody records for regulated studies
    • GLP (Good Laboratory Practice) as required for study-support materials

    Typical usage ratio

    • Varies from 1–10 mol% per specific synthetic route based on client-supplied peptide sequence.
    • Scaled by individual batch run from milligram to multi-gram levels.

    Downstream process integration

    • Direct coupling during manual or automated solution/solid-phase synthesis.
    • Protecting group strategies adapted for compatibility with other sequence blocks.
    • Analytical QC by LC-MS or HPLC of intermediary and final sequence blocks.

    Final product types

    • Custom short peptide libraries
    • Peptide reference standards for bioanalytical assays
    • Specialty peptides for cell research or screening
    • Lead compounds for early-stage drug discovery
    Free Quote

    Competitive D-Leucyl-L-Tyrosine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    D-Leucyl-L-Tyrosine: Manufacturing Insights on a Dipeptide with Real Impact

    D-Leucyl-L-Tyrosine does not always get the attention it deserves in the chemical and life sciences world, but those who work with it know its value. On our production lines, this dipeptide means more than just another name in the catalog. We see requests for D-Leucyl-L-Tyrosine coming from a wide range of sectors, each seeing unique benefits in its molecular profile and performance.

    Origins in the Synthesis Bay: What D-Leucyl-L-Tyrosine Really Is

    Every batch starts with precision-controlled conditions to combine D-leucine and L-tyrosine. We monitor optical activity and purity because the functional characteristics people look for depend on correct stereochemistry. D-Leucyl-L-Tyrosine, by structure, derives from a D-amino acid (leucine) and an L-amino acid (tyrosine), giving it a unique set of properties compared to its all-L or all-D relatives. This duality makes it a subject of interest for researchers in enzymology and peptide therapeutics, since crossing the chiral divide can alter biological activity, resistance to enzymatic degradation, and transport across membranes. Dipeptides with this architecture sometimes slip through biological ‘locks’ in ways single-amino compounds do not—even changing the way they interact with enzymes trying to break them down.

    In scaling up production, we see certain challenges up close—solubility, batch consistency, and purity always at the top of the checklist. Molecules like D-Leucyl-L-Tyrosine, where chiral integrity matters, never give you a free pass. Our teams test every lot by HPLC, specific rotation, and mass spectrometry. No one can afford surprises when the final application could be in pharmaceutical research or biological assay development.

    What Sets D-Leucyl-L-Tyrosine Apart from Its Peptide Cousins

    Many in the field ask about the differences between dipeptides like D-Leucyl-L-Tyrosine and more common ones such as L-Leucyl-L-Tyrosine or L-Leucyl-D-Tyrosine. The main difference—one you can see right on our quality reports—lies in the chirality. D-Leucyl-L-Tyrosine resists breakdown by peptidases that usually target the L-L forms. That resistance makes it an interesting addition for formulations that have to hold up in challenging environments, such as oral dosage or metabolic pathway studies.

    Some customers experiment with both enantiomeric variations, observing shifts in enzyme interactions, transport mechanisms, or substrate competition. In nutritional, cosmetic, and pharmaceutical R&D, researchers pursue these less-traveled stereochemical paths to chase new outcomes. D-Leucyl-L-Tyrosine offers a route to stability and, potentially, altered biological performance—potential you cannot unlock with single-amino acids or L-L dipeptides.

    Model and Specifications: Beyond the Catalog Number

    Bringing D-Leucyl-L-Tyrosine from raw amino acids to pure powder or solution means controlling variables at every stage. We target purity above 98%, focusing on trace contaminant minimization, ash content, water content, and residual solvents. Our staff invests in regular recalibration for every detector and titration rig in our labs. We don’t stop at catalog values, because specs printed on paper do not reflect the reality we uphold in the manufacturing room.

    Customers often ask about physical properties. D-Leucyl-L-Tyrosine usually appears as a white to off-white powder, with solubility values dependent on pH and ionic strength. At a molecular weight of about 324 Da, it packs a short but purposeful backbone. Titration curves, NMR spectra, and mass chromatograms get bundled with every order, so end users can see proof—not just claims—of what they are working with.

    Shipping to both academic and industry partners calls for robust packaging. We recommend storage at cold temperatures and dryness to minimize degradation or hydrolysis. On our end, we use nitrogen purging and moisture-tight containers. We’ve made adjustments over time—in response to real-world feedback—to avoid cake formation or clumping during long transit routes. These details sound minor, but cutting corners in shipping means trouble for researchers down the line.

    Understanding Applications: Where D-Leucyl-L-Tyrosine Earns Its Stripes

    Most of our output finds homes in research settings that push the boundaries of synthetic biology, pharmaceutical screening, and enzymology. Customers working with peptide transporters or trying to understand selective uptake often use this dipeptide as a tracer or a substrate. Its chiral properties show up in kinetic differences in uptake and metabolism, allowing researchers to probe what separates one transport mechanism from another.

    You also see D-Leucyl-L-Tyrosine in studies focused on peptide hydrolysis. Since many mammalian and microbial peptidases act preferentially on L-L bonds, this D-L peptide proves useful in challenge assays or as a reference standard. By comparing it to other stereochemical variants, teams can sort out enzyme selectivity in a level of depth not possible with homochiral peptides.

    Some pharmaceutical investigators use D-Leucyl-L-Tyrosine as a linker or a scaffold in combinatorial chemistry. Its backbone can alter the pharmacokinetics of small-molecule-peptide hybrids or peptidomimetic structures. The dipeptide functions as more than just a spacer—it becomes a dynamic player, modulating resistance to enzymatic breakdown or even drug absorption rates.

    Direct from the Manufacturer: The Daily Challenges and Decisions

    Producing D-Leucyl-L-Tyrosine at scale isn’t without problems. Peptide synthesis, especially where D- and L- components meet, poses stereochemical hurdles. We rely on solid-phase synthesis, with rigorous resin choice and careful deprotection sequences, to ensure yield and chiral purity hold steady batch after batch. Each synthetic run presents an opportunity for error—a stray moisture spike, an incorrectly weighed reagent, or a temperature fluctuation can throw everything off.

    The process never turns into an assembly line. Each lot brings its own challenges, and over time, the staff has learned small tricks—fine-tuning solvents, altering wash times, adjusting cleaving agents. Product quality comes to life not because machines hum quietly, but because humans stand ready to make the right judgment calls. More than once, a batch headed for packaging ended up back in analytical QC because an experienced eye caught an outlier in the NMR or MS data.

    We hear from customers who bought generic Dipeptides elsewhere and wound up with subpar results. Some struggle with baseline noise in chromatograms, others report unexpected biological inactivity, and quite a few run into solubility problems caused by microcontamination. Our philosophy boils down to rigorous process verification from start to finish, so that the material you receive isn’t just another powder in a vial—it’s a compound you can trust for your most sensitive experiments.

    Differences That Matter: D-Leucyl-L-Tyrosine Against the Field

    There’s a world of difference between dipeptides made with L-amino acids and those with mixed chirality. D-Leucyl-L-Tyrosine offers unique resistance to common enzymes, and its stability profile supports longer-term studies. For clients in metabolic or transporter research, these properties make D-Leucyl-L-Tyrosine stand out.

    Compared to single amino acids, dipeptides can bypass certain transport barriers in cells or tissues. The shift from the common L-L profile to D-L enables new pathways for cellular entry. That’s how researchers using our D-Leucyl-L-Tyrosine succeeded in studying non-canonical transport mechanisms—ones not visible with traditional compounds. The product isn’t some wonder chemical, but real science demands a toolkit that sometimes includes niche options like this.

    Accountability and Quality: Our Manufacturing Principles at Work

    Producing D-Leucyl-L-Tyrosine with total accountability isn’t about technology alone. Staff training, continued investment in instrumentation, and feedback loops all matter. We run cross-process audits and blind retesting, bringing together analytics and synthesis to catch anomalies before they affect a shipment.

    Every report comes with detailed analytical data. If a result ever deviates from established standards, we halt release and investigate. Over time, we’ve traced hiccups back to seemingly small factors—imperfect mixing, reagent age, glassware not fully dried. Sometimes, staff pressure us to speed a run for a rush order, but experience shows haste only leads to trouble later.

    Feedback from the lab bench fuels updates in our SOPs. If a customer notes a recurring solubility challenge or finds a novel use for D-Leucyl-L-Tyrosine in transporter studies, we adapt our QC or documentation to support them. We see the relationship as a real partnership. Customers help push us to innovate, and we return the favor with transparency and unyielding standards.

    Batch Consistency: More Than Just a Number

    Batch performance matters more than numbers on a certificate. We’ve seen how even slight shifts in moisture content or byproduct residue can alter downstream biological results. This is especially true for D-Leucyl-L-Tyrosine, where some applications demand microgram-level precision in interaction studies or DNA-peptide conjugation work.

    Every time an order ships, our team reviews analytical trends and customer notes from prior lots, looking for subtle drifts. Being real manufacturers, instead of outsourcers, makes it possible to act on this level of detail. If someone finds a batch underperforming in terms of solubility in a phosphate buffer, or notes curious peaks in the HPLC run, we pull historical data and check if raw material suppliers or synthesis steps may be at fault.

    There’s no off-the-shelf solution to batch consistency. Over the years, we’ve built our processes to catch these invisible variables and to adjust before releases, so clients don’t find variances in their chromatograms. Results matter in the real world, not only the paperwork.

    Looking at Industry Trends: The Future for D-Leucyl-L-Tyrosine

    Research trends keep shifting. We see more customers interested in non-standard peptide structures, perhaps because classic homochiral chemistry only gets you so far in biochemistry or drug development. D-Leucyl-L-Tyrosine’s chiral profile supports applications in peptide transporter studies, proteolysis resistance screens, and even as a linker in complex constructs. It is seeing use in in-vitro modeling to follow the traffic of dipeptide uptake or to control bioavailability in a controlled release formulation.

    Academic research continues to probe how non-natural peptides participate in metabolism. D-Leucyl-L-Tyrosine serves as a practical test case, since its structure can be used to assess transporter specificity or to develop assay standards. Some teams are even using it to build libraries of peptides focused on new diagnostic or therapeutic approaches, trusting that its somewhat unusual backbone brings new options to the table.

    Regulatory Demands and Transparency: Meeting Today’s Standards

    Traceability and documentation no longer happen in the shadows. Our batches track back to raw starting materials, synthetic logs, and QC results for every step. Many customers work under strict regulatory protocol, and we support their compliance with detailed batches and data packages. Fingerprints left by residual solvents or byproducts can no longer hide with modern chemistry scrutiny, and we stand behind our synthesis and purification methods.

    The market is filled with resellers passing off generic materials without a clear source; that’s not us. As manufacturers, we control the process. Should a problem emerge anywhere in our supply chain or production routine, we can find the root and fix it, quickly. Our customers trust that we mean what we say, and each lot of D-Leucyl-L-Tyrosine carries the evidence in every report attached to the shipment.

    Working with Researchers: A Two-Way Street

    Customers bring us new challenges by exploring use cases we may not have encountered before. Some investigate complex protein interactions, others optimize for peptide transport in drug delivery models. Through their feedback, we learn where D-Leucyl-L-Tyrosine delivers and where new improvements are needed. Sometimes this means adjusting particle size to help with mixture handling, sometimes refining purification to eliminate trace artifacts.

    Many of today’s top findings rely on trusted partners able to adapt manufacturing, not just push out catalog numbers. We remain open to collaborating on new variants or custom modifications, fueled by mutual curiosity and a determination to do better with every production run.

    Opportunities and Challenges Ahead

    At the scale we operate, each lot of D-Leucyl-L-Tyrosine represents a challenge answered by skill, testing, and continual adaptation. The future points to growing interest in dipeptides that cross stereochemical boundaries, and we expect demand to rise as researchers chase new biological mysteries. We’ve weathered regulatory changes, supply chain gridlock, and shifting quality benchmarks by holding to standards set by people with years at the bench, not just theories on paper.

    Making D-Leucyl-L-Tyrosine isn’t about only meeting an order; it’s about being trusted for critical work. Producing, purifying, and shipping this compound supports real science, and we take seriously the duty to get each batch right from start to finish.