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HS Code |
293820 |
| Product Name | N'-Cbz-L-Ornithine |
| Chemical Formula | C13H18N2O4 |
| Molecular Weight | 266.29 |
| Cas Number | 7424-03-9 |
| Appearance | White to off-white solid |
| Melting Point | 129-134°C |
| Purity | Typically >98% |
| Storage Temperature | 2-8°C |
| Solubility | Soluble in water and organic solvents (e.g., methanol, ethanol, DMSO) |
| Optical Activity | Specific rotation [α]D20 +18 to +21° (c=1, H2O) |
| Protecting Group | Benzyloxycarbonyl (Cbz) |
| Synonyms | N-alpha-Benzyloxycarbonyl-L-ornithine |
As an accredited N'-Cbz-L-Ornithine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N'-Cbz-L-Ornithine, 25g, is supplied in a sealed amber glass bottle with a screw cap, labeled with product and safety details. |
| Shipping | **Shipping for N'-Cbz-L-Ornithine:** N'-Cbz-L-Ornithine is shipped in secure, sealed containers to prevent contamination and moisture exposure. The chemical is handled according to standard laboratory shipping regulations and may require temperature-controlled packaging. Appropriate labeling and documentation ensure safe and compliant domestic or international transportation as per regulatory guidelines. |
| Storage | N'-Cbz-L-Ornithine should be stored in a tightly sealed container, protected from light and moisture. It is recommended to keep it at 2-8°C (refrigerator temperature) to ensure stability and prevent degradation. Handle in a well-ventilated area and avoid excessive heat. If possible, store under inert gas, such as nitrogen, to avoid oxidation, and always follow appropriate chemical safety protocols. |
Applications of N'-Cbz-L-Ornithine in Industrial ManufacturingN'-Cbz-L-Ornithine, an N-protected amino acid derivative, meets the demanding quality and compliance requirements of the life sciences sector, especially where precision in chiral synthesis and peptide protection is critical. Our manufactured product supports several advanced industrial processes within defined downstream markets. This section details real-world applications based on distinct industry needs and regulatory compliance, strictly focusing on recognized manufacturing scenarios. 1. Peptide Pharmaceutical Intermediate SynthesisSpecialty peptide synthesis facilities utilize N'-Cbz-L-Ornithine as a protected building block to maintain orthogonality during sequential chain elongation, protecting the α-amino group and allowing precise insertion of ornithine residues at controlled positions. Downstream partners depend on its purity and compliance for multi-step solid-phase or solution-phase peptide synthesis destined for APIs and clinical trial materials. Its use is essential to minimize racemization and impurities, directly impacting batch reproducibility and final substance purity. Industry compliance standards
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2. Protected Amino Acid Supply for Custom Peptide CROsContract research organizations engaged in producing custom peptides for preclinical, diagnostic, and research purposes rely on N'-Cbz-L-Ornithine to streamline side chain protection, especially when synthesizing ornithine-containing motifs sensitive to side reaction or cyclization. Tight batch-to-batch quality is critical to their workflows where unique sequences require customized synthetic routes with tailored protection-deprotection schemes. Our product supports these precision requirements by offering reliable purity and consistent protection group stability. Industry compliance standards
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3. Enzyme Substrate Synthesis for Biochemical AssaysBiotech production units that manufacture specialty substrates for enzymatic and protease assays incorporate N'-Cbz-L-Ornithine as a central intermediate for generating calibration peptides. Its carbobenzyloxy (Cbz) group provides necessary stability in further modification steps and purification, which is vital for producing fluorescently or isotopically labeled substrates. This material supports the design of tailored enzyme substrates for pharmaceutical assay and QC labs, meeting stringent requirements for analytical traceability. Industry compliance standards
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4. Advanced Pharmaceutical Research and DevelopmentInnovative pharmaceutical R&D programs employ N'-Cbz-L-Ornithine to explore ornithine analogs for structure-activity relationship (SAR) studies, macrocycle design, and next-generation peptide drug platforms. Its protected form enables introduction into synthetic routes that require site-specific deprotection or orthogonal chemistry, without compromising the integrity of complex multi-residue scaffolding. Consistent QC documentation and impurity tracking remain central to its uptake in process development and lead optimization laboratories. Industry compliance standards
Typical usage ratio
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N-Cbz-L-Ornithine plays an essential role in the world of peptide synthesis and specialty intermediates. As chemists working every day to transform raw materials into value for our partners, we understand how even a single amino acid derivative can become a limiting factor—or an enabler—for research, scale-up, and manufacturing. Through consistent process control and attention to molecular detail, we've built our N-Cbz-L-Ornithine line not only for purity on paper, but for performance in the flask and reliability in the long run.
Our manufacturing team starts each batch of N-Cbz-L-Ornithine with pharmaceutical-grade L-ornithine. Every kilo comes from well-documented origins, handled in dedicated areas to avoid cross-contamination. The Cbz (carbobenzyloxy) protection step follows protocols developed over years of routine use, but we never allow ourselves to treat routine as mindless repetition. Operators regularly validate reactor conditions, reagent addition, and environmental safety at every scale we offer, whether from grams or metric tons.
Hydrogenolysis, recrystallization, and advanced filtration help us reach typical purities exceeding 99% by HPLC, but high purity alone tells only part of the story. Partner labs report that our material arrives with free-flowing, bright white crystals—no aggregated lumps, fused particles, or persistent dust. These physical characteristics trace back to how we control precipitation rates, solvent dryness, and temperature ramping. The practical result is easier weighing and dissolution with fewer handling losses downstream.
Our production teams have kept N-Cbz-L-Ornithine within tight identity and content targets, both for the main compound and for all known impurities. The Cbz group is particularly sensitive to over-protection, and by limiting byproduct formation through careful catalysis and post-treatment, we help users avoid costly purification steps. Typical specifications include:
Every batch carries full QC documentation. These results come from trained in-house analysts working on maintained equipment—never from passed-on reports or aggregated broker certificates. The differences show up in customer feedback, and repeat users comment that our material requires little or no additional drying for coupling reactions or library synthesis.
Chemists know the pitfalls that come with suboptimal building blocks. For peptides, the presence of excess protecting groups or byproducts can sabotage coupling reactions, generate side-chains, or inflate purification time. Our N-Cbz-L-Ornithine has become a foundation for research teams looking for consistency and transparency, particularly where lysine analogs or urea bridge formation come into play. Laboratories pursuing GEO or cyclic peptide frameworks report that smooth deprotection cycles and minimal colored residues during work-up make a measurable difference in project timelines.
Contract manufacturers often remark that switching to our product reduces failed batches and intervention calls. With so many novel peptide drugs under development, delays at the amino acid stage can hold up combinatorial campaigns, solid-phase assembly, or process validation.
As a chemical manufacturing team, we know that trust starts with process transparency. Full traceability from raw material lot through to final packaging remains a core value, demanded by qualified buyers and internal QA alike. For regulated markets and future patent challenges, access to original process runs and analytical logs gives our partners the data required to support endotoxin statements, impurity profiles, and solvent residual audits.
We maintain a harmonized digital system instead of relying on stacks of paper in binders. Physical retention samples, calibration logs, and SOP deviation records are held on-site for the required audit period as per ISO and cGMP standards. Routine vendor qualification, including on-the-ground site visits for critical reagents, ensures upstream controls remain robust.
The Cbz protecting group, or benzyloxycarbonyl, offers special advantages in peptide chemistry, and our long production history with these derivatives lets us exploit its strengths. Cbz blocks unwanted amine reactions while showing orthogonality toward acid and mild base conditions—essential in multistep peptide assembly. By calibrating hydrogenation and work-up steps, we avoid over-reduction or partial cleavage that can lead to mixed products.
Compared to other protected ornithines, such as Boc-L-ornithine, the Cbz group can be selectively removed under catalytic hydrogenation, which fits high-throughput protocols and parallel library methods. By holding impurity formation well below typical market levels, users rarely face column fouling, broad peaks, or hard-to-identify byproducts during downstream deprotection.
We’ve seen both large pharma and start-up labs wrestle with decisions between ornithine building blocks—ranging from Fmoc- and Boc- to unprotected amines. Out of these, N-Cbz-L-Ornithine brings reliable balance between protection, handle-ability, and manageable deprotection protocols. Boc-protected materials, for instance, require strong acid removal (often TFA), which may not suit acid-sensitive side chains or delicate scaffolds. Fmoc analogs involve base lability, which narrows compatibility with some protecting strategies.
Research teams facing potential side-chain branching or lysine mimic structures choose Cbz for its ease of removal without overexposing the growing peptide to harsh chemistry. From our perspective, feedback points to fewer side-chain racemization events, and low rates of epimerization during coupling, leading to more predictable product identity—a vital point in later-scale up or regulatory submission.
Batch-to-batch consistency matters. Vendors promising low-cost materials often fall short in real-use metrics such as filterability, solubility in polar aprotic solvents, or chiral retention. Having observed failed coupling reactions and unexpected TLC profiles from off-brand imports, we’ve focused our manufacturing protocols on supply stability, impurity reduction, and reproducibility—even during seasonal demand spikes.
We operate under ongoing scrutiny for sourcing, waste reduction, and greenhouse gas minimization. Starting with bio-derived L-ornithine, we continuously work to minimize non-renewable content and optimize solvent reuse. Our operators receive regular training in green chemistry principles, and process engineering teams stay current with best practices to cut emissions and lower energy consumption in hydrogenation, crystallization, and drying.
In downstream packing, reducing single-use plastics remains a work in progress, but we have transitioned bulk shipments to recyclable or reusable containers where possible. Buyers concerned with scope 3 emissions or ESG audits often call on us for origin documentation and process energy footprint details, and we keep these records live and accessible for review. This level of accountability pays off in trusted, long-term business relationships—particularly as new regs take shape in Asia, North America, and the EU.
Every method has its challenges. For N-Cbz-L-Ornithine, two persistent hurdles affect both the bench and the plant: byproduct control and residual solvent management. Cbz-protection often generates benzyl alcohol or dibenzyl urea byproducts, which—if left unchecked—can tail into the desired fraction or foul columns at the purification step.
To counter these, we introduced low-temperature, staged addition protocols and fine-particle filtration, trimming extraneous peaks on the chromatogram. For solvent loads, rotary evaporation under vacuum, plus well-ventilated tray drying, allow us to guarantee levels in line with pharmacopoeia limits. Routine staff training ensures solvent grade selection fits the reaction rather than legacy practice, especially as regulatory cutoffs shift. We encourage end users to routinely check their own incoming solvents and provide specification sheets for every lot.
Another operational concern spins around the variable demand for protected amino acids. Industry shifts—from biopharmaceuticals to diagnostics—can cause raw material bottlenecks. We hedge our sourcing with multi-country supply options and buffer stocks, protecting against both regional disruptions and annual market swings. Repeat collaboration with peptide CDMOs and R&D groups gives us early signals, so we can scale production in anticipation, avoiding rationing or extended lead times that damage both parties’ project flow.
We don’t market ourselves through claims alone; we back up quality differences with shared reference spectra, side-by-side competitor studies, and real-user feedback. After fielding reports from labs frustrated with poor filtration rates or persistent tails during reverse-phase HPLC, we re-optimized crystallization for better particle size homogeneity. Customer-driven QA challenges have led to process tweaks—like neutralizing rinse cycles and closed-loop filtration—to reach cleaner, more reproducible product with every drum.
For those operating under tight regulatory regimes, we’ve provided on-site support and rapid requalification, including full method transfer for analytical and prep-scale work. Many start with a few test grams, then come back for multi-kilo repeat runs after confirming labor savings and lower troubleshooting time.
Long-term users point out not just purity, but improved coupling efficiency, reduced color in product streams, and less gelling or clogging of peptide purification setups. These “real-life wins” stem from material born of practice, not repackaging. At the core, the ingredient works for users because we never lose focus on its role as part of a multi-step system—delivering on specifications that matter in the context of real-world chemistry.
Our team participates in international consortia and technical working groups focused on both process innovation and regulatory science. Keeping communication frequent with academic partners, contract manufacturing organizations, and biotech start-ups lets us adapt quickly to new application demands and technical hurdles—from unusual cyclization conditions to non-peptide frameworks that call for specific solubility and reactivity traits.
The next wave of advances will likely come from intensified process analytics—continuous reaction monitoring, digital batch records, and AI-assisted process modeling. Day-to-day, we encourage customer labs to reach out with performance feedback, impurity concerns, or new requirements. Only by connecting documentation with practical challenges can we tune material quality for tomorrow’s advances, not just yesterday’s regulations.
N-Cbz-L-Ornithine marks more than just a protected amino acid—it’s a product of persistent, hands-on improvement, built on real production floors for actual chemical research and scaled manufacturing. From our plant operators to technical advisors, we value the hard details: crystal habit, impurity profile, side reaction rates, and user support—all tuned to keep projects on track and discoveries moving forward. In an evolving landscape of chemistry and manufacturing, this direct line between daily plant operations and research impact shapes every batch we deliver, keeping reliability and accountability at our core.