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HS Code |
352843 |
| Chemical Name | N-Alpha-Acetyl-L-Arginine |
| Cas Number | 3582-29-2 |
| Molecular Formula | C8H16N4O3 |
| Molecular Weight | 216.24 |
| Appearance | White to off-white powder |
| Solubility In Water | Soluble |
| Melting Point | 196-200°C (dec.) |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Synonyms | Acetyl-L-arginine, N-Acetyl-L-arginine |
| Usage | Biochemical research, supplement ingredient |
| Ph Of 1 Percent Solution | 5.0-7.0 |
| Stability | Stable under recommended storage conditions |
| Ec Number | 222-683-7 |
| Inchi Key | AKYAXZJZHJEUCE-ZETCQYMHSA-N |
As an accredited N-Alpha-Acetyl-L-Arginine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 100 grams of N-Alpha-Acetyl-L-Arginine, sealed with a tamper-evident cap and labeled for laboratory use. |
| Shipping | N-Alpha-Acetyl-L-Arginine is shipped in tightly sealed containers to prevent moisture and contamination. It is typically sent at ambient temperature unless otherwise specified. All packaging adheres to chemical safety regulations, and includes clear labeling for identification and hazard information. Shipping documentation ensures compliance with international transport standards for non-hazardous chemicals. |
| Storage | N-Alpha-Acetyl-L-Arginine should be stored in a tightly sealed container, protected from light and moisture. Store at room temperature, ideally between 2–8°C (36–46°F), unless otherwise specified by the manufacturer. Keep the chemical in a dry, cool, and well-ventilated area, away from incompatible substances and sources of ignition. Follow all relevant safety guidelines when handling and storing. |
Applications of N-Alpha-Acetyl-L-Arginine in Industrial ManufacturingAs a direct producer of N-Alpha-Acetyl-L-Arginine, we supply this ingredient to several advanced manufacturing sectors requiring precise formulation, validated compliance, and traceable supply chains. Below, we outline real downstream industry applications with detailed integration, compliance, and product-specific information. 1. Pharmaceutical Formulation: Injectable Nutrition and Parenteral SolutionsN-Alpha-Acetyl-L-Arginine serves as a stable arginine derivative in sterile injectable preparations, especially total parenteral nutrition (TPN) formulas. Its stability under autoclave conditions and compatibility with amino acid blends facilitate straightforward compounding without detectable precipitation or pH drift in infusion solutions. Clinical nutrition producers favor its improved metabolic profile and lower risk of bacterial degradation relative to unmodified arginine during thermal sterilization. Industry compliance standards
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2. Functional Food and Nutraceutical PowdersFood supplement manufacturers use N-Alpha-Acetyl-L-Arginine as a direct-acting arginine source in sports and health powders where enhanced gastrointestinal stability and controlled arginine release matter. Compared to standard L-arginine, this derivative limits degradation in flavored beverage mixes and high-acid matrices, reducing off-taste and shelf-life issues. Production-level blending exploits its improved solubility to achieve uniform doses per serving. Industry compliance standards
Typical usage ratio
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3. Peptide Synthesis and Biopharmaceutical ProductionCROs and biopharma companies utilize N-Alpha-Acetyl-L-Arginine as a protected amino acid in solid-phase peptide synthesis (SPPS). Its blocked alpha amino group simplifies the construction of sequence-specific arginine-containing peptides without undesired side reactions or chain terminations. This material achieves high stepwise coupling yields due to minimal racemization, improving batch reproducibility in pilot and scale-up runs for custom peptides and APIs. Industry compliance standards
Typical usage ratio
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4. Cell Culture and Biotechnology FermentationBiotechnology and vaccine manufacturers employ N-Alpha-Acetyl-L-Arginine in custom cell culture media and fermentation broths. It provides a stable, cell-permeable arginine source supporting high cell proliferation and recombinant protein yields, especially in mammalian and CHO cell lines. Its acetylation reduces rapid destruction by arginases in the medium, ensuring more consistent amino acid nutrition profiles and minimizing ammonia byproducts. Industry compliance standards
Typical usage ratio
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Our shop floor often buzzes around the reactors dedicated to N-Alpha-Acetyl-L-Arginine. Over the past decade, we've focused on this compound because feedback from laboratories and specialty nutraceutical companies points to a recurring need for purity, predictable handling, and consistent quality. Ultimately, that's what keeps research running smoothly and finished formulations performing as intended. We have spent years honing our process to minimize batch variation and optimize flow, which helps researchers and product developers focus on applications without interference from trace-level byproducts or off-notes in organoleptic testing.
Ask a biochemist or a formulation scientist why they reach for N-Alpha-Acetyl-L-Arginine rather than the simple L-Arginine salt, and the answers highlight real-world obstacles. L-Arginine can break down or oxidize under certain conditions, becoming unpredictable when project timelines demand reliability. Acetylating the amino group increases overall compound stability, so shipping across continents or storing in fluctuating climates no longer raises concern. Our customers in peptide synthesis and nutritional research say the difference shows during stress testing: where raw L-Arginine sometimes yields inconsistent results in extended-release blends or complex assays, the acetylated form remains stable thanks to its altered chemical structure. That translates into fewer headaches for anyone who depends on reproducible data or shelf-stable finished products.
Scaling N-Alpha-Acetyl-L-Arginine presents lessons that don’t always make it into textbooks. Small batches synthesized in glassware let us spot color changes or precipitation, but translating these steps to larger reactors introduced new twists—runaway reactions and the occasional clogged filter. We invested in tailored purification methods, using both modern chromatography and classical crystallization, to tighten our specifications. After two years dialling in parameters, we standardized product flow so each drum, whether destined for Asia or the Americas, delivers a consistent free-flowing powder. We regularly pull random retention samples, running independent HPLC and FTIR scans in our own QC lab to ensure quality never wavers. Our team recognizes that a single bottleneck or supplier hiccup could mean missed deadlines. Redundancy in both utilities and precursor sourcing keeps the line moving with minimal downtime.
On the shop floor, we commit to an assay purity exceeding 98.5%, based on HPLC. Moisture content sits below 1.0%, a level validated by Karl Fischer titration weekly from multiple batches. Customers working on injectables or high-end medical nutrition appreciate the low endotoxin and heavy metal readings, which we keep well below stringent international thresholds. Granule size and flow properties affect both how machines handle the powder and how formulas behave in end use. The attention to muscle memory on the packaging line, careful use of anti-static liners, and rigorous batch documentation reflect years spent investigating why certain customers faced clumping or inconsistent blending. Standard packing runs from one-kilo foil bags up to drums, each inerted under nitrogen. This approach became necessary after a large shipment a few years ago spent ten days in customs in a humid port city and still arrived with specs intact.
Chemists sometimes debate between using L-Arginine, its hydrochloride salt, or the more stable acetylated version. Each brings its own strengths. L-Arginine remains the workhorse for basic cell culture or pharmaceutical synthesis when cost is the main driver. The HCl salt rises in popularity whenever water solubility counts most or when buffering is critical. High-performance or pharmaceutical blends increasingly opt for N-Alpha-Acetyl-L-Arginine to avoid the oxidative instability and high reactivity that can plague less modified forms. Acetylation shields the amino group, reducing sensitivity to temperature, pH, and typical storage stressors. We’ve seen pharmaceutical customers report fewer surprises during stability testing in applications where compliance means strict batch-to-batch reproducibility. For nutrition applications, the acetylated form provides a milder taste with fewer off-flavors, helping formulators hit palatability targets, a significant challenge in protein fortification.
Each customer segment approaches this material differently. Peptide manufacturers favor N-Alpha-Acetyl-L-Arginine when seeking amide bond protection during stepwise assembly. The N-acetyl group serves as a handle that simplifies downstream processing. Analytical labs appreciate how the increased stability removes variables in enzyme assays, making it easier to compare results across lengthy experiments. Brands working in sports nutrition or medical food formulation look for the compound because it brings both functional and sensory advantages over traditional amino acids. Researchers investigating novel arginine derivatives share how the acetylated variant better mimics natural modifications observed in complex protein pathways. Our ongoing collaboration with universities helps refine which parameters get prioritized in manufacturing—tight pH control, absence of residual solvents, and lot-to-lot reproducibility. These requests reflect practical barriers that pure researchers and industrial applications face when scaling from bench scale curiosity to pilot and commercial launches.
The distance between our reactors and a customer’s lab can span time zones and unpredictable customs delays. Customers in Southeast Asia point to monsoon humidity, while those in Central Europe manage variable transit times in winter. N-Alpha-Acetyl-L-Arginine’s increased chemical stability makes it an ideal cargo for these conditions. Recently, a shipment bound for a facility in Brazil spent close to three weeks in storage due to a logistics strike. The product performance remained unchanged, and assay readings matched the retention sample held at our factory. This isn’t theory—these are shipment logs, stability test reports, and customer QC files that have come across our desks. Over the years, most transport headaches stem from inadequate packaging or insufficient documentation, so we emphasize tamper-evident seals and comprehensive lot tracking. These simple but effective measures assure our customers that each container carries the same material they sampled before scaling up their production lines.
Leading up to scale-up for a new medical nutrition product, one of our customers requested full transparency on impurities and trace metal content. Our QC team produced certificate of analysis records for multiple batches, including microbial and heavy metal profiles. The customer’s own lab tested side-by-side with our records, and their specifications matched, which supports external audits and compliance with European and North American regulatory standards. Over the years, as requests for detailed origin and traceability information increased, we invested in digital batch recordkeeping. QR codes on each drum now access batch manufacturing and analytical data, giving procurement managers and regulatory staff a real-time view of production history and quality control findings. This documentation isn’t just about box checking for audits—it helps end users trust that the raw materials align with their finished product claims. We have seen customers use these records to expedite market entry or resolve customs clearing questions faster.
In our early years, customers flagged inconsistent yield and powder clumping with the first iterations of N-Alpha-Acetyl-L-Arginine. Through conversations with formulation scientists and on-site visits to contract manufacturers, we pinpointed moisture uptake during final milling as a culprit. By installing inline dehumidification and retraining operators on best drying practices, we reduced out-of-spec events to near zero. Not everything changes with equipment upgrades, though—building staff skills on how to quickly identify subtle color or texture changes made a bigger difference than any policy manual. This hands-on troubleshooting, paired with traceable batch analytics, now forms the backbone of our quality system. Whenever feedback suggests even minor shifts in blending or reactivity patterns, our technical team cross-examines the raw material lots and adjusts processing parameters on the next production cycle. These direct feedback loops ensure our output keeps pace with both regulatory shifts and changing customer needs.
We’ve assembled a portfolio of amino acid derivatives, but N-Alpha-Acetyl-L-Arginine receives more attention for several reasons. Pharmaceutical and nutraceutical partners frequently cite regulatory expectations for impurities and consistency; this product meets or surpasses most benchmarks in pharmacopeial monographs. A broader pool of nutrition brands sees increasing value in acetylated variants because they better manage flavor profile and oxidative stability in protein formulations, which is key for ready-to-drink or bar formats. Our production teams appreciate fewer storage concerns and longer shelf stability compared to highly sensitive amino acid precursors. Customer requests for both small R&D samples and multi-ton orders enable us to fine-tune logistics for both laboratory and commercial scale projects. All feedback received translates to further enhancements in standard operating procedures—each improvement gets stress-tested by both lab and end-user feedback.
As global regulators continue tightening purity, allergen, and trace contamination limits for inputs in food and pharma production, N-Alpha-Acetyl-L-Arginine production has had to adapt. Compliance with standards from US, European, and Japanese pharmacopeias now drives ingredient projects, and we tailor analytics accordingly. Certifications for GMP, ISO, and upcoming requirements from major private standard-setters like NSF mean regular, unscheduled audits. Internal teams practice for these audits using blind batch trails and cross-site mock recalls. Regulatory trends also increasingly demand full provenance for intermediates and utilities, from solvents to water purification. Some nations require original digitally signed batch histories for customs clearance, so we built our database to export cryptographically verifiable production records on request.
Years of industry partnerships have sharpened our ears for hidden barriers. Early, we focused just on purity and price. International formulation houses pointed to powder compaction and stickiness that slowed their blending equipment. Troubleshooting these issues demanded an overhaul in how we measured caking and powder flow. Now, we benchmark every batch using customer-oriented performance tests rather than just laboratory metrics. Peptide chemistry labs needed precise end-point reactions, so trace residual solvent analysis became routine. Nutrition researchers grappling with taste problems in protein fortifiers needed surface modification—our development chemists engaged with them to measure bitterness reduction after acetylation. Each cycle of customer input leads to either process changes or new product variants. This iterative process shaped the robust, adaptable product we now offer.
Walking through the applications built using our N-Alpha-Acetyl-L-Arginine, a few trends emerge. Contract manufacturers working on parenteral and enteral nutrition turn to the acetylated derivative, given its reduced reactivity and consistent pH behavior, which directly impacts shelf life and product safety. Sports performance brands incorporate it into high-end amino acid blends, aiming for smoother taste and longer product stability. Startup research labs rely on acetyl-L-Arginine as a standard for enzyme assays and chiral analysis—its stability and known purity ensure that assay drift or reagent decomposition cannot cloud the experimental results. In peptide synthesis, the protected amino group simplifies multi-step reactions and increases the yield of target fragments.
Anecdotes collected from researchers over the years reveal practical challenges—shipping failures, reagent degradation, or unpredictable color changes. Acetylated derivatives like N-Alpha-Acetyl-L-Arginine answer these with their chemical and physical robustness. Production managers at manufacturing sites mention simpler storage logistics and easier inventory planning, because the improved shelf life lessens the risk of urgent reorders or shipment failures. This compound offers a bridge between cutting-edge research and mainstream product development, something raw L-Arginine or even its HCl salts rarely achieve in parallel.
Producing specialty amino acids generates solvent and side product waste, which previously demanded significant energy expenditure to neutralize or recycle. We upgraded our solvent recovery systems, now reclaiming more than three-quarters of the organic solvents used in the acetylation steps, which dramatically lowers both raw material costs and environmental impact. Process water is recirculated following purification, reducing overall site water consumption. Customers increasingly ask about carbon footprint and waste management, so we share verified environmental performance reports covering our production cycles for each lot. Technical staff coordinate with external auditors annually to review waste management, energy consumption, and emission controls. These measures grew from both internal sustainability goals and market pressure from customers who now base supplier selection on verified environmental improvements.
Investments in automation and analytics have changed our daily workflow on the production floor. Automated dispensing controls reagents in real time, cutting manual intervention and nearly eliminating batch variability. In-line monitoring lets our chemists spot changes in pH, conductivity, or color that could point to process drifts before a batch so much as leaves the kettle. We’ve built a habit of reviewing customer complaints and suggestions during internal reviews. Sometimes, even the sharpest analytical lab cannot replicate the complex handling or mixing conditions faced in a customer’s commercial environment. Whenever a shipment feedback reveals an unexpected caking event, the team investigates everything from line speed to ambient humidity, then adjusts production or packaging protocols. Each improvement, large or small, builds trust and speeds adoption for the next generation of lab or product formulation.
In the years since we started producing N-Alpha-Acetyl-L-Arginine, demand has shifted from simple purity to a more holistic expectation—consistent output, traceable origin, and shared responsibility for sustainability. We take pride in our open-door feedback policy. Anyone sourcing our compounds can access batch histories, analytical records, and supportive regulatory documentation without waiting for weeks. For us, the product starts with raw materials and ends with feedback from its last end-user, whether that’s a research scientist or a manufacturing line supervisor. As regulatory standards and industrial use cases keep evolving, we adapt in kind—constantly learning and updating our approach, so that the next batch not only matches your assay standard but supports the full life cycle of high-quality, stable, and reliable products.