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L-Leucyl-L-Alanine

    • Product Name L-Leucyl-L-Alanine
    • Alias H-Leu-Ala-OH
    • Einecs 248-962-2
    • 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

    768960

    Name L-Leucyl-L-Alanine
    Cas Number 2478-20-8
    Molecular Formula C9H18N2O3
    Molecular Weight 202.25
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point 250-255 °C (dec.)
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Iupac Name (2S)-2-[(2S)-2-amino-4-methylpentanamido]propanoic acid
    Synonyms Leu-Ala, H-Leu-Ala-OH
    Ec Number 219-607-2

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

    Packing & Storage
    Packing White plastic bottle with secure screw cap, labeled "L-Leucyl-L-Alanine, 25g," featuring hazard symbols, batch number, and storage instructions.
    Shipping L-Leucyl-L-Alanine is typically shipped in tightly sealed containers to protect it from moisture and contamination. The product should be transported at room temperature, away from direct sunlight and incompatible substances. Standard shipping regulations for non-hazardous chemicals apply; ensure proper labeling and documentation for safe handling and delivery.
    Storage L-Leucyl-L-Alanine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of moisture. Store at 2-8°C (refrigerator) for optimal stability. Keep away from incompatible substances such as strong oxidizers. Always follow appropriate laboratory safety protocols and refer to the material safety data sheet (MSDS) for specific storage recommendations.
    Application of L-Leucyl-L-Alanine

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

    As a precision manufacturer of L-Leucyl-L-Alanine, we supply this dipeptide to established global companies across specialized sectors. Below, we detail verified downstream applications, compliance frameworks, industrial usage ratios, production process integration stages, and the final product types delivered to end markets.

    1. Peptide Pharmaceutical Intermediates

    L-Leucyl-L-Alanine serves as a reliable building block for active pharmaceutical ingredient (API) synthesis, particularly in the manufacture of peptide-based drugs. Controlled use ensures batch accuracy and reproducibility required by regulated drug production. Manufacturers introduce it during solid-phase or solution-phase peptide synthesis, supporting efficient elongation and introducing specific functional moieties. Its purity and traceability meet stringent pharma requirements for regulated marketing authorization.

    Industry compliance standards

    • cGMP (Current Good Manufacturing Practice, ICH Q7 guidelines)
    • Ph. Eur. (European Pharmacopoeia, Monograph 2034)
    • USP (United States Pharmacopeia standards for peptide APIs)
    • ICH Q3A/B (Impurity and residual solvent limits)

    Typical usage ratio

    • 2–20% molar feed based on fragment sequence length; exact ratio tailored to peptide chain design and yield optimization

    Downstream process integration

    • Integrated as a protected or free dipeptide during pre-assembly or fragment coupling in solid-phase synthesis columns or automated peptide synthesizers

    Final product types

    • GMP-grade peptide APIs for metabolic disorders
    • Peptide-based prodrugs and diagnostic agents
    • Functionalized fragment intermediates for custom peptide libraries
    • Reference standards for pharmaceutical QC

    2. Nutraceutical Manufacturing (Peptide-Enriched Supplements)

    Nutrition companies use L-Leucyl-L-Alanine to enhance amino acid profiles in dietary supplements targeting performance and muscle recovery. The material offers defined peptide structure, enabling predictable bioavailability and taste-masking effects. Food safety and labeling regulations direct raw material selection and strictly govern addition during formulation blending under HACCP or ISO 22000 controls.

    Industry compliance standards

    • FSMA (FDA Food Safety Modernization Act for ingredient safety)
    • ISO 22000 (Food Safety Management System)
    • EU Commission Regulation (EC) No 1333/2008 on Food Additives
    • GB 2760 (Chinese Food Additives National Standard)

    Typical usage ratio

    • 0.1–2% w/w in active blend, depending on product type and desired amino acid content; adjusted for protein supplementation matrix and target demographic

    Downstream process integration

    • Added during main blending operation in supplement premixes or direct-compression tablet lines; also used in powder mixes for functional sports nutrition

    Final product types

    • Peptide-enriched nutraceutical tablets and capsules
    • Functional amino acid drink powders
    • Recovery protein bars and sports beverages
    • Specialized senior nutrition blends

    3. Cell Culture Media Additive in Biotechnology

    Biotech companies rely on high-purity L-Leucyl-L-Alanine for supplementing animal, bacterial, or yeast cell culture media. As a nitrogen and carbon source, it supports optimized cell growth and protein expression, especially for recombinant protein production. Quality controls enforce source traceability, low endotoxin profiles, and sterility validation in line with industry and regulatory standards.

    Industry compliance standards

    • ISO 13485 (Medical Devices Quality Management for bioprocessing)
    • USP <1043> (Ancillary Materials for Cell, Gene, and Tissue-Engineered Products)
    • EMA Guideline on the Use of TSE-Risk Materials
    • CFR 21 Part 211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 10–200 mg/L of culture media; precise level optimized based on target cell line requirements and protein yield response

    Downstream process integration

    • Introduced during aseptic preparation of basal or feed media before sterilization step; may be filtered inline to maintain media purity

    Final product types

    • Recombinant monoclonal antibodies
    • Industrial enzymes and biotherapeutics
    • Cell-based research kits and media packs
    • Hybridoma and stem cell culture reagents

    4. Protease Substrate in Enzymatic Assays

    Diagnostic reagent and analytical kit manufacturers choose L-Leucyl-L-Alanine as a selective substrate for measuring protease activity, especially in high-throughput biochemical testing. The defined dipeptide structure amplifies assay specificity and enables kinetic analysis of serine and cysteine proteases. Batch-to-batch consistency and analytical traceability are central to reliable downstream kit manufacturing and clinical laboratory use.

    Industry compliance standards

    • ISO 13485 (Medical Device Quality Management Systems)
    • IVDD 98/79/EC (EU Directive on in vitro diagnostic medical devices)
    • USP <1225> (Validation of Compendial Procedures)
    • CLSI EP5-A2 (Evaluation of Precision Performance of Quantitative Measurement Methods)

    Typical usage ratio

    • 50–500 µM in assay buffer; recipe tailored to enzyme specificity and detection system sensitivity

    Downstream process integration

    • Precisely measured and dissolved in reaction buffers during automated filling or kit formulation at diagnostic reagent manufacturing sites

    Final product types

    • Enzyme activity assay kits
    • Clinical chemistry reagents for hospital labs
    • Protease profiling panels for drug screening
    • Research-grade fluorometric or colorimetric substrates

    5. Reference Material for Analytical Method Validation

    Accredited laboratories utilize high-purity L-Leucyl-L-Alanine as a reference standard for the calibration and validation of chromatographic and spectrophotometric methods. The molecule’s predictable retention profile and defined purity enable reproducible method development for peptide analytics, quantitation, and impurity profiling. Sourcing and use follow international best practices for quality and safety in laboratory environments.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • ICH Q2(R1) (Validation of Analytical Procedures)
    • USP <621> (Chromatography)
    • Ph. Eur. Section 2.2.46 (Chromatographic Separation Techniques)

    Typical usage ratio

    • Calibration standards: 1–100 µg/mL in mobile phase or diluent; tailored to instrument detection limits and sensitivity requirements

    Downstream process integration

    • Prepared in analytical sample vials or as spike-in standards before method validation, system suitability, or calibration checks in regulated lab workflows

    Final product types

    • Certified reference materials (CRMs) for HPLC, UPLC, and LC-MS
    • Quality control calibration kits for pharma/bioanalytics
    • Analytical proficiency testing panels
    • System qualification cartridges for instrument vendors
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    Certification & Compliance
    More Introduction

    L-Leucyl-L-Alanine: Precision and Reliability in Peptide Building

    Turning Laboratory Ambitions Into Real-World Results

    Working every day with L-Leucyl-L-Alanine, our team understands the demands researchers and manufacturers face with peptide synthesis. Each lot produced in our plant passes through years of know-how. We’ve watched requests change: some focus on increasing yield, others on improving purity. L-Leucyl-L-Alanine, or Leu-Ala, consistently answers the call because it captures two critical amino acid side chains in a way that enables downstream processes to move quickly while minimizing error. This dipeptide’s structure merges the branched-chain hydrophobic nature of leucine with the compact, functional simplicity of alanine—a choice that balances reactivity and stability better than similar building blocks.

    The model most often requested sits at the white crystalline powder grade, tailored specifically for synthetic chemistry and pharmaceutical R&D. Clients range from pharmaceutical labs seeking short, reproducible synthesis cycles to academic groups focused on mechanistic protein research. In our experience, purity above 98% reduces the risk of byproducts interrupting coupling reactions or contaminating downstream assays. We guarantee this not through off-the-shelf sourcing but from controlling every stage of manufacture. Our reactors operate in closed systems, protecting each batch from trace water and airborne contaminants, which matter immensely at gram and kilogram scale.

    Why L-Leucyl-L-Alanine Matters: Real Use Cases From the Factory Floor

    Our team supplies this dipeptide to organizations pushing boundaries in enzyme substrate studies and drug discovery platforms. Frequently, a project leader comes to us facing a bottleneck in peptide sequence extension. Substitution with L-Leucyl-L-Alanine simplifies chain assembly, particularly where steric bulk or hydrophobicity could derail a sensitive synthesis. The leucine moiety introduces side-chain complexity that serves programs looking to mimic in vivo protein folding, while the alanine end delivers structural consistency without unnecessary weight or reactivity. Whether preparing peptidomimetics or functionalized peptide tags, users can run long reactions with minimal risk of side-chain scrambling or racemization. Early in our years producing Leu-Ala, we realized batch uniformity and crystal morphology determine how consistently the product works in automated synthesizers, so this element receives routine in-house focus.

    For use in laboratory-scale solid-phase synthesis, our L-Leucyl-L-Alanine's solubility in water and common organic solvents allows high-loading resins to swell and interact directly without requiring multiple solvent exchanges. Researchers often tell us switching from single amino acid coupling to dipeptide coupling saves both time and reagents during sequence assembly. Cycle times drop, costs follow, and analytical results improve because fewer byproducts emerge from each step. Several manufacturing clients apply our material in enzymatic and chemical hydrolysis studies because the molecule’s conformation sits close to certain native protein linkages—the dipeptide nearly mimics a section of natural polypeptide backbone. This similarity brings a real-world advantage in enzyme kinetic work where cleavage specificity can make or break an assay.

    Specification Insights: More Than Just a Molecular Formula

    Producing L-Leucyl-L-Alanine in-house, our plant doesn’t settle for minimum specification thresholds. We maintain regular lot sampling, with high-resolution analytical equipment set up for monitoring not only peptide purity but also physical parameters like bulk density and melting point. Because many clients dose our product directly into reactors or use it to charge multiwell assay plates, variations in powder texture and flow can complicate scale-up and contribute to electrostatic losses or dosing errors. Over several years, we’ve fine-tuned our crystallization and drying steps, yielding a free-flowing, low-fixture powder. We see orders come in both for standard multi-gram research packs and tens-of-kilos for pilot plant use, with both scales held to identical specifications.

    One frequent discussion with clients revolves around moisture content. Even a small percentage of water can throw off calculated stoichiometry in tightly controlled coupling reactions. Our approach guarantees residual moisture sits at or below 0.5%, and every lot receives a Karl Fischer titration before shipping. This attention reduces reaction unpredictability and supports long-term shelf stability, a fact that’s particularly valued by pharmaceutical developers who may warehouse chemicals for months awaiting project go-ahead.

    The optical rotation value for our batches is always measured and logged, ensuring each shipment remains consistent for stereospecific applications. Dipeptide impurities and decomposition products undergo regular scrutiny via HPLC and mass spectrometry. This practice helps clients meet stringent regulatory or reporting requirements when the product moves from research-grade status to the edge of preclinical trial material. Client audits, common in our industry, have repeatedly confirmed that our internal controls reduce both cross-contamination and the need for retesting.

    L-Leucyl-L-Alanine vs. Other Dipeptides: Practical Differences From Daily Use

    From our vantage inside production, Leu-Ala’s main difference from other dipeptides such as Leu-Leu, Ala-Ala, or Gly-Leu rests in the way it behaves across reaction conditions. For example, double alanine dipeptides offer lower molecular weight and higher flexibility, but fail to introduce the same hydrophobic bulk needed in studies modeling transmembrane or intracellular domains. On the other hand, Leu-Leu runs heavier, hydrophobic, and sometimes delivers lower solubility—even modest degrees of aggregation slow or disrupt every second step of a synthesis. Researchers tackling sequence-specific or functional site analysis turn to Leu-Ala because it closely mimics an active-site section of certain enzymes, yet dissolves and reacts rapidly—a time-saving trait inside every run.

    From a manufacturing perspective, we monitor the effects of substrate selection on dipeptide purity and throughput. Raw material cleanliness drives final product clarity, especially where chiral centers make small racemization problems hard to visually catch but significant in end-use performance. Substituting Leu-Ala for generic dipeptides often brings cleaner reaction profiles, easier purification, and greater yield after lyophilization.

    Talking regularly with long-time customers, the feedback centers on reliability across synthesis batches. Chemists recall switching from unrefined dipeptide sources and observing unplanned peaks or noisy chromatograms disappear—often translating to more reproducible biological data. In our own QC, we have mapped these changes to both our reaction staging (kept under controlled temperature and agitation) and to tight in-process monitoring, something direct manufacturers have the power to execute and adjust mid-process in ways that distributors or traders cannot.

    Supporting the Real World Beyond the Bench

    Behind every order of L-Leucyl-L-Alanine stands an experienced team responding daily to specific formulation and experimental challenges. Our technical staff often walks customers through best methods for dissolution, coupling protocols, or post-run clean-up—even translating decades of combined practical feedback into subtle changes in production. One example arose from a medical research hospital: adjusting our drying cycle by just a few degrees improved the ease of weighing for high-throughput robotic synthesis stations. These day-to-day tweaks accumulate, adding up in manufacturing robustness and helping reduce avoidable delays in the laboratory.

    Scale matters in this industry. Small research packs must deliver performance equal to commercial offerings. For one pharmaceutical API developer, we developed a custom packaging solution because their regulatory framework specified storage under inert gas. Many clients working under GMP conditions turn to us for point-by-point validation documents outlining everything from reactor window cleaning schedules to final lot sign-off dates. Working as a primary manufacturer gives us insights (and direct control) into how our materials can stand up to lengthy stability trials, comprehensive impurity checks, and evolving customer testing environments. Leu-Ala outperforms outsourced material in our direct side-by-side evaluations—not just in purity but also in the reliability of supply and ongoing technical support.

    Meeting New Demands: Sustainability, Safety, and Traceability

    Over the past decade, we have watched chemical manufacturing standards rise across the industry. L-Leucyl-L-Alanine production now demands not just purity and reliability, but a transparent trail of raw material sourcing and process waste handling. We’re adapting by choosing suppliers with documented environmental performance and by investing internally in closed-loop solvent recovery systems—a move that saves resources and reassures clients looking for lower environmental impact. Annual audits by third-party environmental consultants confirm these advances, and our safety record for solvent emissions improves each year.

    On the safety front, handling and packaging protocols reflect real-world laboratory and plant risks. Every staff member receives regular training on exposure prevention, cleanroom discipline, and spill response. Our facilities house dedicated storage and transfer areas, equipped to minimize cross-contamination with other products. Direct feedback from partner labs influences our improvements. One large-volume user, after reporting static electricity problems in powder transfers, guided our team to install advanced grounding stations, cutting down both losses and potential dust ignition risks. These ongoing changes highlight the value of keeping close connections with the people actually using our chemicals.

    Traceability forms a key part of pharmaceutical and diagnostic material supply today. L-Leucyl-L-Alanine leaving our production line carries full batch history, from initial amino acid input down to final lots tested for residual solvents and particle size. Our records are open to customers—audited as part of their vendor qualification protocols or for their own regulatory submissions. These same detailed archives assist us if an issue is raised, enabling rapid root cause analysis and corrective action. Long-term, our commitment to transparency and customer partnership has driven repeat business among leading biopharmaceutical firms and research institutions alike.

    Challenges in Peptide Chemistry: Lessons From the Field

    Sourcing high-purity dipeptides often falls short when relying on generic bulk suppliers. We hear repeatedly from project leaders facing unexpected impurities, under-validated batch histories, or inconsistent product solubilities. Technical surprises—failed couplings, incomplete deprotection, or troublesome side reactions—cost time and blunt research momentum. Direct engagement between manufacturer and end user replaces anxiety with real-time answers. One client in protein modification research traced an erratic set of reaction yields not to their protocols nor to instrument drift, but to a fluctuating impurity profile in the dipeptide received from a broker. Once we established a direct supply, reaction results stabilized and synthesis rates improved.

    From our side, keeping up with the changing complexity of peptide targets isn’t easy. Each emerging technique in peptide conjugation, backbone modification, or unnatural amino acid insertion brings new requirements for precursor quality. Our lab staff invest significant hours in method development and troubleshooting, mapping how every tweak in process or purification alters customer results. We favor open conversation: process engineers and chemists openly discuss best methods for peptide handling, solid support selection, and compatibility with divergent coupling reagents. Through this feedback loop, our internal processes have reduced side-product formation rates and improved customer yields over time.

    Looking Forward: Commitment To Quality and Collaboration

    For synthetic chemists and manufacturers alike, L-Leucyl-L-Alanine represents more than a simple dipeptide. It is a tested tool backed by decades of industrial process improvement, continuous peer inquiry, and long-term customer partnership. Our experience leads us to invest in process robustness as much as purity metrics—understanding the practical, everyday challenges that crop up far beyond what a data sheet can capture.

    New research programs ask for rapidly available quantities, clear technical documentation, and responsive support. We are positioned to meet these demands through rigorous internal controls and direct lines of communication. Each lot of L-Leucyl-L-Alanine stands as a testament to our ongoing efforts—melding hands-on production know-how with a dedication to supporting those pushing peptide and protein science forward.

    Trust in a chemical supplier comes from more than a certificate of analysis—it builds from shared experience, mutual accountability, and clear demonstration of technical and ethical responsibility. We welcome these expectations. As the uses of L-Leucyl-L-Alanine and related building blocks expand, we remain committed to offering practical support and quality materials for every laboratory and production environment.