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

L-Ornithine

    • Product Name L-Ornithine
    • Alias ornithine
    • Einecs 210-510-8
    • 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

    516823

    Name L-Ornithine
    Chemical Formula C5H12N2O2
    Molar Mass 132.16 g/mol
    Appearance White crystalline powder
    Solubility In Water Very soluble
    Melting Point 223-226 °C
    Cas Number 70-26-8
    Amino Acid Type Non-proteinogenic
    Ph Value 5.7-6.1 (1% solution)
    Usage Dietary supplement
    Biosynthesis Urea cycle intermediate
    Taste Slightly bitter
    Boiling Point Decomposes before boiling
    Storage Conditions Cool, dry place

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

    Packing & Storage
    Packing L-Ornithine is packaged in a sealed, white plastic bottle containing 100 grams, labeled with product name, purity, and safety information.
    Shipping L-Ornithine is typically shipped as a white crystalline powder in securely sealed, labeled containers to prevent contamination and moisture exposure. The shipment complies with standard chemical handling protocols, including appropriate cushioning and documentation. This non-hazardous amino acid is generally shipped at ambient temperature, but should be kept dry and protected from light.
    Storage L-Ornithine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances. Protect it from moisture and direct sunlight. Recommended storage temperature is typically room temperature (15–25°C). Proper labeling and secure storage are essential to prevent contamination and ensure safety. Always follow the manufacturer's guidelines and safety data sheet instructions.
    Application of L-Ornithine

    Applications of L-Ornithine in Industrial Manufacturing

    L-Ornithine is a specialty amino acid applied as a functional additive and intermediate across multiple regulated industrial sectors. As an experienced manufacturer, we supply high-purity L-Ornithine tailored to the needs of strictly controlled downstream industries. Below, you will find typical application fields, compliance standards, representative usage ratios, process integration points, and the types of final products manufactured with L-Ornithine.

    1. Pharmaceutical Ingredient for Hepatic Support Formulations

    Pharmaceutical producers incorporate L-Ornithine into medical compositions targeting liver function management, especially for hyperammonemia and hepatic encephalopathy therapies. Companies develop oral and parenteral drugs using ornithine salts (e.g., ornithine aspartate, ornithine hydrochloride) where strict regulatory oversight requires certified raw material sourcing and traceability. Compliance with international pharmacopeias and GMP regulations governs every stage, from raw material receipt to tableting, encapsulation, or sterile solution compounding. End products are delivered as prescription oral powders, injectable vials, or granules, often under combination schemes for liver detoxification protocols.

    Industry compliance standards

    • USP (United States Pharmacopeia)
    • EP (European Pharmacopoeia)
    • ICH Q7 GMP guidelines
    • 21 CFR 210/211 (US FDA GMP for finished drugs)
    • ChP (Chinese Pharmacopoeia) for domestic registration

    Typical usage ratio

    • 20–50% in oral powders (combined with other amino acids, excipients)
    • 5–12% in intravenous solutions (as ornithine aspartate, based on treatment regimen)
    • Ratio adjusted by formulation, indication, and specific salt form requirements

    Downstream process integration

    • Dissolving and reacting in solution tanks for API synthesis
    • Pre-blending with bulking agents before granulation or tableting
    • Sterile filtration and filling for injectable formulations

    Final product types

    • Oral granules for hepatic failure care
    • Injectable ampoules for ammonia detoxification
    • Combination amino acid tablets for liver and urea cycle support

    2. Dietary Supplement Manufacturing

    Nutritional supplement producers use L-Ornithine for sports, endurance, and health enhancement formulas marketed under food-grade regulations. The manufacturing process handles blending with other amino acids (such as arginine), vitamins, and minerals in powder or capsule form. Manufacturing plants maintain HACCP or FSSC 22000 certification, and formulations require adherence to country-specific food additive codes. During production, L-Ornithine is dosed according to declared daily intake values, with batch-to-batch uniformity validated by in-house QC. Finished supplements support marketed claims such as muscle recovery, fatigue reduction, or growth hormone promotion.

    Industry compliance standards

    • ISO 22000 / FSSC 22000 (Food Safety Management Systems)
    • FDA 21 CFR 111 (US Dietary Supplement GMP)
    • EFSA Food Additive Registry (Europe)
    • GB 29924 (China Food Additive Standard for Amino Acids)

    Typical usage ratio

    • 2–10% in blend (high-protein powder mixes)
    • 200–1000 mg per capsule/tablet (precisely portioned by batch recipe)
    • Dose per serving controlled by regional regulations and declared function

    Downstream process integration

    • Direct blending with compatible amino acids, flavorings, and sweeteners
    • Wet or dry granulation for tableting
    • Capsule filling on automated lines

    Final product types

    • Powdered sports nutrition blends
    • Functional health drink sachets
    • Amino acid complex capsules
    • Single-ingredient health tablets

    3. Clinical and Enteral Nutrition Production

    Producers of clinical nutrition solutions and specialized enteral feeds add L-Ornithine to enhance nitrogen balance and support metabolic function in compromised patients. Application occurs in formulating ready-to-feed liquids, high-protein formulas for ICU/kidney/liver patients, and nutritional recovery products under strict medical food oversight. Manufacturers must meet regional guidelines for medical nutrition, including contamination control and comprehensive product traceability. During large-scale batching, L-Ornithine is solubilized and combined with proteins, carbohydrates, and micronutrients under validated conditions to prevent degradation and ensure bioavailability.

    Industry compliance standards

    • ISO 13485 (Medical Device and Medical Food Production)
    • EU Regulation (EU) No 609/2013 (Foods for Special Medical Purposes)
    • GB 29922 (China FSMP Standard)
    • Codex Alimentarius CAC/GL 10-1979 (General standard for medical foods)

    Typical usage ratio

    • 0.1–1% of total formulation (based on protein/amino acid profile design)
    • Adjusted for nitrogen contribution and compatibility with disease-specific requirements

    Downstream process integration

    • Precise dosing into homogenizing tanks during bulk solution preparation
    • Quality control for amino acid composition and sterility before aseptic filling
    • Monitoring pH and temperature to prevent ornithine degradation in finished product

    Final product types

    • Enteral tube feeding solutions
    • Oral clinical nutrition beverages
    • High-protein ICU recovery diets

    4. Biotechnological Fermentation Enhancer

    Industrial biotech companies employ L-Ornithine as a metabolic activator or nitrogen source in large-scale microbial or cell culture fermentations, optimizing the biosynthesis of specific amino acids, secondary metabolites, or recombinant proteins. Regulatory focus includes raw material qualification and in-process monitoring governed by pharma or industrial food standards when outputs target pharmaceutical or food use. L-Ornithine is usually introduced during inoculum development or main batch fermentation stages, allowing for increased yields and specific metabolite pathways activation. Downstream operators test substrate assimilability and adjust integration to minimize by-product accumulation and enhance yield.

    Industry compliance standards

    • ICH Q7/Q11 guidelines for biotech APIs
    • ISO 9001/14001 for plant process control
    • Food Chemicals Codex (FCC) for food- and pharma-grade production

    Typical usage ratio

    • 0.05–0.3% per fermentation batch (optimized based on desired output and microorganism type)
    • Real-time adjustment based on in-situ metabolite and nitrogen monitoring

    Downstream process integration

    • Feeding into bioreactors during secondary metabolite synthesis stage
    • Pre-conditioning of inoculation media
    • Process monitoring with nutrient substrate balancing

    Final product types

    • L-Arginine, L-Citrulline, and derivatives produced by fermentation
    • Pharmaceutical-grade bioproducts
    • Fermentation-based food additives

    5. Animal Nutrition Premixes and Veterinary Formulations

    Feed and veterinary product manufacturers utilize L-Ornithine to enhance growth, immune status, and nitrogen utilization in demanding animal husbandry contexts, especially for high-yielding poultry, aquaculture, and specialty livestock. Animal feed applications follow national and international safety and labeling standards. Manufacturers add ornithine into powdered premixes, soluble additives, or injectable veterinary drugs, carefully balancing inclusion to fit animal species, growth stage, and environmental stressors. Downstream plants blend ornithine with other amino acids, vitamins, or minerals before extrusion, pelleting, or liquid dosing.

    Industry compliance standards

    • EU Regulation No 183/2005 (Feed Hygiene)
    • AAFCO (US Association of American Feed Control Officials) ingredient definitions
    • GB/T 16767 (China Feed Additive Standards)
    • ISO 22000/HACCP for feed plant operations

    Typical usage ratio

    • 0.01–0.1% in compound feed, depending on species and application target
    • 0.1–0.5% in vitamin/amino acid premix blends
    • Concentration selected by animal nutritional needs and formulation

    Downstream process integration

    • Dry blending for premix manufacture
    • Mixing with water-soluble vitamins for liquid concentrates
    • Direct dosing in injectable veterinary products

    Final product types

    • Livestock and aquaculture nutritional premixes
    • Compound animal feeds
    • Oral drench and injectable veterinary specials
    Free Quote

    Competitive L-Ornithine 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 admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    L-Ornithine: A Closer Look at a Key Amino Acid in Industry and Health

    Understanding L-Ornithine from the Manufacturer’s Perspective

    Working with amino acids over the decades has taught us something crucial: what matters most isn’t just purity or compliance, but a manufacturer’s attention to every single reaction and every step in handling, from the raw material through crystallization and packaging. L-Ornithine, with its white crystalline appearance and unique handling characteristics, has become one of those compounds where process experience and day-in-day-out quality control really show their value. By dealing with every batch ourselves, we see the entire life of each production lot—its consistency, its quirks, and why customers across food, feed, pharmaceutical, and cosmetic sectors raise specific questions or run into recurring challenges.

    To start, L-Ornithine deserves a bit of context. It doesn’t fall in the group of proteinogenic amino acids—the type that gets coded directly into proteins. Instead, it is a non-protein amino acid essential for the urea cycle, allowing cells to process and detoxify ammonia. This function makes it vital for health and metabolic tasks, and also shapes how it is demanded in industrial and specialty applications.

    Our L-Ornithine is available as the free base, boasting a chemical formula of C5H12N2O2, and is manufactured under strict GMP conditions. The material has a molecular weight of 132.16. Consistently, we supply this product as a white, odorless powder with high solubility in water. Most often, we strive for purity levels above 99%, verified by HPLC, not just for regulatory compliance but because downstream processes—be it tablet pressing, powder blending, or precise formulation—leave little room for off-spec lots. Each shipment undergoes rigorous heavy metal and microbial testing, a non-negotiable in the food and pharma supply chain.

    Why L-Ornithine Matters Beyond Standard Protein Nutrition

    Talking directly with pharmaceutical clients, we hear concerns that extend past what standard bulk resellers express. For instance, L-Ornithine supports ammonia detoxification; it does not simply serve as a building block, but enhances metabolic processes in a unique way. This trait leads to real impact in therapeutics for liver support products, clinical nutrition, and even recovery formulas where muscle fatigue and metabolic balance count. The feedback loop from clinicians and supplement formulators reminds us that our processing diligence—eliminating traces of structurally related byproducts, preventing unwanted salt forms, and maintaining clean room standards—ends up right in the consumer’s hands.

    Health supplement manufacturers come to us asking not only about crystalline particle size or shelf life, but how L-Ornithine interacts with arginine, citrulline, and glutamine in their blends. They know the value of transparent manufacturing. Unlike some raw material brokers, a manufacturer stands behind test results with logs, not just paperwork. We invest in technical training for our QA staff so they recognize issues before a batch leaves the site—a decision that does not always reflect directly on a COA but changes the outcome for the end user.

    Compared to L-Arginine or L-Citrulline, L-Ornithine fits a different metabolic niche. While arginine gets more attention for supporting nitric oxide production, ornithine’s role in removing excess nitrogen from tissues gives it a unique advantage in liver health and metabolic support. Customers often conflate these amino acids, so we share the practical insight that arginine conversion to ornithine happens in the hepatocytes. Still, supplementing directly with ornithine bypasses some metabolic bottlenecks, which can lead to different clinical outcomes. This nuance appears in our technical bulletins and is reinforced in technical visits and customer calls, because buying decisions depend on understanding these subtle differences.

    Precision in Manufacturing Means Reliable Product Every Time

    Every product batch undergoes multiple crystallizations to ensure the final powder remains bright white and free of off-odors. Moisture control matters, especially in tropic and sub-tropic climates; we store and ship L-Ornithine in double-lined drums with food-grade liners to avoid caking or hydrolysis. That decision came directly from a batch that failed visual inspection back in the factory’s early years, and customer feedback since then proves its worth. Real improvements in shelf life and flow characteristics come from day-to-day tweaks, not distant policy memos.

    Each year, as environmental standards tighten, we choose non-solvent and eco-friendly purification steps where possible. Early in our production experience, we shifted away from legacy purification using harsh chemicals. Instead, we adopted water-based and membrane filtration for intermediate steps, which improves downstream processability and helps meet sustainability goals. This switch not only protects staff but means no residual solvents end up in the drum. These technical choices often go unnoticed until a customer’s regulatory inspection turns up questions; here, a transparent chain of custody and a detailed batch record make all the difference.

    Several grades exist—chiefly, pharmaceutical and food grades, but also versions tailored for animal nutrition. Animal nutrition requires just as much care. We saw animal feed blenders adopt ornithine to help with muscle-building in performance horses and other livestock. Consistency and absence of contaminants ensure those applications perform as expected; any shortcut in processing shows up down the line, not just in laboratory reports.

    Regulatory and Quality Realities Shape Supply Choices

    Regulatory demands keep evolving in every region. Customers demand BRC, ISO, GMP, FSSC22000, and sometimes even stricter standards. These are not just paper exercises but require audits, traceable process maps, and detailed recall contingency plans. Our compliance team meets face-to-face with auditors, and after many years we’ve found that having genuine on-site control over microbial, heavy metal, and cross-contamination risks shortens audit times and increases confidence. Our international clients need valid Halal and Kosher certifications, so we host routine external reviews and never let certificates lapse; each department remains accountable, right up to packaging and shipping.

    Nothing replaces real traceability. Traders and drop-shippers might promise origin data, but only manufacturers can walk a customer through every part of production, from fermentation tank to finished drum. Over the years, we switched from synthetic starting materials to bio-fermentation with select strains, which brings a continuous supply while lowering environmental footprint. Each lot number tells a traceable story—raw material source, core process changes, staff interventions, adjustments for seasonality. That level of transparency isn’t a customer demand alone—it keeps our entire operation honest and continually improving.

    Applications Reach Across Sectors—Each Bringing Its Own Challenges

    Dietary supplements absorb the largest share of our L-Ornithine, especially in Asian, European, and North American markets. Large-scale contract manufacturers want every kilogram certified, and they demand rapid response on every COA question. Our production records from the last 15 years show a trend toward tighter impurity profiles, with buyers more sophisticated and less tolerant of batch-to-batch variation—even at the parts-per-million level. Many supplement brands now invest heavily in third-party testing, so we encourage this kind of oversight, which keeps the supply chain vigilant and maintains product confidence at retail.

    Pharmaceutical uses can’t afford shortcuts or contamination. Companies working with parenteral or oral formulations routinely review our batch records, stability data, and reference standards. The difference between a technical grade and pharma grade comes down to validation, but more often to how issues are managed in real time. Twenty-four-hour monitoring, in-process controls, and staff empowered to halt production prevent errors rather than manage them after shipment. We see this in customer audits; the more transparent our process, the more partners ask us for solutions to complex issues—say, a sudden change in particle morphology or an unexpected trace element in a finished lot.

    Animal nutrition processors use L-Ornithine to boost feed profiles, aiming for improved muscle recovery and overall animal health. The feedback loop works both ways; veterinarian trials and feedlot results feed into production tweaks or even changes in standard analytical methods. In one project, a customer’s report about off-odors at high humidity led us to modify drying steps and change packaging protocol. These collaborative efforts help address unique sector concerns not always visible from a laboratory or office.

    Cosmetic brands increasingly seek ultra-pure L-Ornithine for use in anti-aging creams and skin-rejuvenation blends. Here, trace contaminants can affect texture, stability, or even color, so our process eliminates secondary amines, residual solvents, and metallic ions. Product managers and R&D chemists will sometimes visit the manufacturing site themselves—they know the proof is on the factory floor, not just in a marketing claim.

    L-Ornithine's Unique Features Compared to Other Amino Acids

    Amidst the explosion of amino acid products on the market, L-Ornithine’s unique value often gets overlooked by those new to ingredient selection. Unlike L-Arginine, which is often used to increase vasodilation or boost circulation, ornithine functions as a direct participant in the urea cycle. Its main value is not as a nitric oxide donor, but as a remover of waste nitrogen, reducing blood ammonia concentrations during intense athletic training, metabolic stress, or certain clinical conditions.

    Customers sometimes expect one amino acid to substitute for another, but real-world processes say otherwise. Manufacturing personnel can share dozens of examples where an attempt to swap L-Citrulline or L-Arginine for L-Ornithine in a formulation led to compromised solubility, storage issues, or different end-user results. These field reports reinforce the idea that products are not interchangeable, especially when demanded attributes include long-term stability and complete dissolution.

    Practical experience highlights that L-Ornithine, in spite of being structurally close to other amino acids, can withstand broader pH ranges without breakdown. It flourishes in blends with certain vitamins and minerals and doesn’t promote browning in soft gel and powder manufacturing—a frequent issue with reactive amines. This stability leads major supplement houses and clinical nutrition brands to choose it over similar amino acids when a neutral taste and robust shelf-life are non-negotiable.

    Solving Real-World Problems—Quality, Storage, & Logistics

    Manufacturing responses to on-the-ground challenges set professional producers apart from mere distributors. Take storage. L-Ornithine’s hygroscopicity matters in countries with high ambient humidity. If poorly packed, product can clump or degrade. We responded by overhauling packing lines, adopting inert gas flushing, and adding additional QA checkpoints at drum-sealing stations. Freight-forwarders working in hot, humid ports appreciate these measures, as do formulation chemists who blend powder in climate-sensitive environments.

    An experienced manufacturer pays attention to loading schedules and transport, timing shipments to minimize transit delays—especially critical for pharma and food customers subject to seasonal peaks. Our own fleet and preferred logistics partners coordinate to deliver direct to customer, bypassing storage at uncontrolled third-party warehouses. This approach reduces the risk of thermal cycling, accidental contamination, and helps maintain compliance year-round.

    Unexpected issues come up. Recently, a shipment meant for a high-altitude facility arrived with altered particle size distribution, traced back to vibrational shock in cross-continental shipping. Fixes in both packaging and advisory notes for clients solved the problem for future lots. It’s not always a dramatic story, but over time, each of these improvements filters into everyday SOPs, preventing recurrences and saving time and money for everyone along the supply chain.

    Transparency, Authenticity, and What Only a Real Manufacturer Can Offer

    For some, L-Ornithine is just another item in a long ingredient list. To a manufacturer, it represents a living case study in how small process improvements and relentless attention to raw material flow create a real difference for customers. With every batch we produce, decisions made years ago play out as practical advantages: lower contaminant levels, consistent solubility, longer shelf life, and a comfort customers value when they contact us directly with technical questions.

    Laboratory control provides only part of the story. Operators on the production floor can identify subtle shifts in odor or texture long before machines pick them up. Experienced eyes and hands, with dozens of years’ collective experience, avoid faults that slip by at a less attentive facility. We openly invite customer audits and sampling at every stage; these exchanges create strong working relationships and build trust not just between companies, but among the scientists and technologists who make the industry’s work possible.

    Looking Ahead—Adapting to Market Needs and New Applications

    The world of amino acids evolves constantly. Customers push for lower residual thresholds, non-GMO assurances, and new niche applications in functional foods and personalized nutrition. Decades ago, large manufacturers could set the tone. Today, the best insights travel rapidly down the supply chain, often from clinician and end-user right back to the factory floor. We keep laboratory and production staff engaged with current research, encourage attendance at technical conferences, and maintain an open-door policy for commercial partners.

    Our approach uses steady process improvement and a willingness to troubleshoot production problems directly with customers, a method that creates mutual value and ensures our L-Ornithine meets tomorrow’s demands—not just today’s. In a fast-moving field, real manufacturing experience provides the anchor. Trust, access, and product quality flow not from slogans but from a consistent record earned batch by batch.