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HS Code |
978556 |
| Name | Fmoc-Lys-OH |
| Full Name | N-α-Fmoc-L-lysine |
| Molecular Formula | C21H24N2O4 |
| Molecular Weight | 368.43 |
| Cas Number | 35661-40-6 |
| Purity | ≥98% |
| Appearance | white to off-white powder |
| Solubility | soluble in DMF, DMSO, and methanol |
| Storage Temperature | 2-8°C |
| Protecting Group | Fmoc (fluorenylmethyloxycarbonyl) |
| Amino Acid Type | L-lysine derivative |
| Application | used in solid phase peptide synthesis |
As an accredited Fmoc-Lys-OH factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Fmoc-Lys-OH is packaged in a sealed amber glass bottle, containing 5 grams, with clear labeling for safety and identification. |
| Shipping | Fmoc-Lys-OH is shipped in sealed, moisture-proof packaging to ensure chemical stability and prevent contamination. It is typically dispatched at ambient temperature, unless otherwise specified by the manufacturer. Appropriate labeling and documentation following chemical safety regulations are provided, facilitating secure transport and compliant delivery to laboratories or research facilities. |
| Storage | Fmoc-Lys-OH should be stored in a tightly sealed container at 2–8 °C (refrigerated) in a dry, well-ventilated area, protected from light and moisture. Avoid prolonged exposure to air to prevent degradation. Keep away from incompatible substances, such as strong acids or bases. Use proper personal protective equipment during handling. For long-term storage, store under inert gas if possible. |
Applications of Fmoc-Lys-OH in Industrial ManufacturingFmoc-Lys-OH operates as a key protected amino acid building block in multiple high-value industries. Our facility manufactures this material for direct use in advanced peptide and protein synthesis, pharmaceuticals, diagnostics, biomaterials, and research reagents. Each sector utilizes distinct technical protocols, regulatory systems, and downstream integrations to ensure manufacturing consistency and compliance. 1. Pharmaceutical Peptide SynthesisPharmaceutical companies utilize Fmoc-Lys-OH as a protected lysine derivative during stepwise solid-phase peptide synthesis (SPPS) for active pharmaceutical ingredient (API) production. The material enters at the sequential chain elongation stage using Fmoc/t-Bu protocols, with precise deprotection and coupling cycles. Manufacturing process design follows strict GMP controls, impurity profiles, and traceability for therapeutic-grade peptides. Innovation in drug discovery and generic peptide drugs often depends on reliable sourcing of protected amino acids meeting global guidelines. Industry compliance standards
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2. Diagnostic Peptide Kit ProductionPeptide-based diagnostic kits require precise synthesis of bioactive sequences containing lysine residues, often with Fmoc-protected intermediates. Industrial kit manufacturers incorporate this material during solid-phase or solution-phase peptide synthesis for assembly of specific epitopes or tags. High batch-to-batch fidelity and ultralow contamination levels remain essential, as these products interface with immunoassays and molecular diagnostics across clinical laboratories. Industry compliance standards
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3. Biomaterials and Tissue Engineering ScaffoldsBiomedical companies leverage Fmoc-Lys-OH to prepare functionalized peptides used in hydrogel, nanofiber, and scaffold applications for tissue engineering. The protected lysine provides bioorthogonal handles for selective modification, integrin binding, or crosslinking. Raw material integrates during custom peptide chain design intended for biocompatible scaffolds, requiring trace impurity analysis and consistent functional group protection throughout multi-step fabrication workflows. Industry compliance standards
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4. Custom Research Peptide Synthesis ServicesProfessional peptide synthesis services rely on high-purity Fmoc-Lys-OH to fulfill diverse academic and commercial custom orders. This includes structure–activity relationship studies, protein engineering, and tagged peptide generation for proteomics or molecular biology applications. Strict material traceability and impurity profiling support protocols demanded by university labs, CROs, and biotech firms. Researchers often require rapid batching, sequence flexibility, and validated analytical data from material suppliers. Industry compliance standards
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Competitive Fmoc-Lys-OH prices that fit your budget—flexible terms and customized quotes for every order.
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Fmoc-Lys-OH, full name Nα-Fmoc-Nε-Boc-L-lysine, stands as a genuine building block for professionals committed to peptide synthesis. As hands-on producers, we understand the daily realities of scale-up, batch consistency, and the nuance in amino acid selection that many downstream users experience. Over the years, we’ve often fielded questions about why this particular lysine derivative has become a mainstay on peptide synthesizers worldwide, so let’s dig in.
Making Fmoc-Lys-OH is no back-office operation. Stringent process design, regular equipment calibration, precise atmospheric controls—are integral on every manufacturing day. We have fine-tuned our process so our batches repeatedly hit a typical purity at or above 99.0%, supported by HPLC data. Our production lines accommodate bulk synthesis without skimping on purity or facing batch-to-batch deviations. Tech teams in our facilities frequently cross-verify amino acid content using both HPLC and titration, not because the market demands it, but because minimizing microvariances supports solid performance in automated synthesis.
Standard packaging ranges from 100g bottles for discovery labs up to 25kg industrial drums. Our team maintains strict lot control and chain of custody for every package leaving our site. Each container includes a unique batch reference code, simplifying any downstream quality review or traceability needs. For those running cGMP processes, our documentation trails are robust, always including full CoAs and method-of-analysis transparency.
Our Fmoc-Lys-OH gets wide adoption because it solves some baked-in headaches in synthesis. Unlike wholly unprotected lysine or amino derivatives with aggressive deblocking groups, our product brings a double layer of protection—the Fmoc group shields the alpha amino position, while the side chain’s epsilon amino sits under Boc protection. This design limits unwanted side reactions, especially during high-loading steps or with challenging sequences. In practice, we see that even when resin loading hits full tilt, side chain acylation rarely creeps in. That reliability matters for those producing clinical-grade APIs or long-chain peptides, where one unprotected amine can mean hours lost and resources wasted.
No two labs use identical methods, but some pain points stay universal. Base-induced racemization creeps up faster with certain amino functions unprotected. Our Fmoc-Lys-OH gives peptide chemists a far wider process window. There’s no need to baby the pH or restrict coupling times; our product handles base conditions with the kind of resilience you want at scale or in difficult sequences. We see huge demand from CROs and CDMOs synthesizing custom peptides with pharmacological activity, but even academic labs prefer our Fmoc-Lys-OH for pilot studies where reproducibility is king.
Peptide synthesis is not a one-size-fits-all world. The side chain of lysine, rich in its propensity for secondary reactions, calls for both selectivity and protection. In solid phase peptide synthesis (SPPS), our Fmoc-Lys-OH integrates seamlessly with standard Fmoc protocols, fitting processes that rely on either manual or automated synthesizers. Deprotection proceeds under mild bases like piperidine; the Fmoc group lifts cleanly, avoiding significant byproduct formation that would otherwise slow downstream purification.
The Boc group on the ε-amino survives these base treatments, standing up to the entire sequence until the final acidolysis. What does that mean for actual peptide builds? It means protected lysine sites stay inert, and site-specific modifications stand a chance to come out right in a single cycle. This dual protection empowers users to create linear, branched, or even dendritic peptide structures on the first shot, instead of repeating work due to unwanted cross-linking.
Years spent manufacturing this compound have shown us that consistency is no accident. Variability stems from solvent quality, precursor selection, reaction temperature stability, and purification conditions. Minor shifts here snowball into larger analytical problems for customers, especially as they prepare for regulatory filings or scale-up batches.
We invest in analytical controls that many in the market overlook until problems surface after delivery. Our QC cycle frequently includes mass spectrometry, elemental analysis, and moisture testing using Karl Fischer titration, all tailored specifically for amino acid derivatives like Fmoc-Lys-OH. We’ve found that subtle differences, such as micro-particulate content or water absorption during storage, can shift how well the product dissolves in DMF or NMP. Real-world users working at hundreds of grams to kilogram scales depend on this predictability, especially for high-throughput production lines.
Comparing with other lysine forms underlines why so many turn to our Fmoc-Lys-OH. Use of unprotected lysine (Lys-OH) or mono-protected variants (Boc-Lys-OH or Ac-Lys-OH) can create more capping steps and side-chain activation risks—a little slip, and you see reduced yields or hard-to-purify crude material. Clogs, lower purities, smearing on HPLC, and wasteful purification become common. Our Fmoc-Lys-OH, with its dual protection, protects chemists from many of these common snags.
Contrast this to Fmoc-Lys(Boc)-OH analogues that miss the mark on purity. Some competitors’ products come in brownish powders or carry solvent residues; we insist on a white to off-white solid, with residual solvent levels below 0.1% as checked by GC. We often receive requests for custom particle sizing, especially when users run fluidized bed reactors and demand uniform dissolution rates. Unlike generic traders, our in-house milling and sieving capacity accommodate special cuts, so dissolution in polar aprotic solvents meets the tightest standards.
One key area driving Fmoc-Lys-OH demand is therapeutic peptide development. As APIs become more complex and sequences grow longer, failure rates on resin increase with even slight inconsistencies in monomer quality. Many labs push their columns harder—higher throughput on synthesisers, lower solvent cycles, and denser resin. That can expose vulnerabilities in low-grade raw materials. An impure or inconsistent amino acid derivative leads directly to yield hits, contaminant peaks, and project delays. Over years of direct collaboration, we have gathered feedback that our high-purity batches produce predictably clean HPLC traces, fewer deletion sequences, and robust yields, making the leap from R&D to clinical manufacturing achievable.
This holds especially true for GMP-regulated API production. We support both ID testing and extended impurity profiling, as many regulatory bodies demand precise tracking of potential contaminants down to the ppm level. Our documentation doesn’t stop at the CoA; we routinely assist with customer audits, supply site-specific data, and provide additional analytics like LAL endotoxin tests for injectable-grade materials.
The landscape of peptide therapeutics shifts year-on-year, with new modalities, novel conjugations, and mounting regulatory expectations. Amid this complexity, reliability becomes more than a box to tick—it’s a foundation for entire drug development programs. By tuning our synthesis routes, investing in cleanroom environments, and adapting purification based on customer process needs, we give researchers and developers what they want: an Fmoc-Lys-OH they can rely on from mg scale all the way up to multi-kg lots.
Our investment in scale provides both cost competitiveness and the flexibility to deliver freshly produced material according to usage cycles. There’s no waiting for resellers to clear warehouse stock—our direct customer feedback shapes production planning, reducing lead times and letting our R&D chemists troubleshoot or tweak batches without red tape.
Our technical support team collaborates with users long after a batch leaves the plant. Peptide chains that struggle with solubility or tend to aggregate can often trace their problems to precursor variability or water content. We’ve logged hundreds of customer queries covering every imaginable pitfall, from resin swelling discrepancies to sluggish coupling. Our material routinely wins confidence in both batch and continuous flow synthesis, as data show less aggregation and lower batch reprocessing rates.
For tougher sequences like branching or cyclization, the dual-protected form of our Fmoc-Lys-OH opens up routes that would be tricky—or nearly impossible—with less protected forms. Some synthetic chemists save hours using our material by skipping auxiliary protecting group manipulations, resin re-swelling, and unnecessary coupling repeats. Cost savings stack up not just in reagents, but in labor and time, an area that’s often underestimated until one runs up against regulatory submission deadlines or production bottlenecks.
We don’t shy away from the real environmental impact of peptide chemical manufacturing, either. Our engineering group works with local environmental agencies and industry bodies to minimize discharge and optimize solvent recapture at every stage of Fmoc-Lys-OH production. On-site solvent recovery units process DMF, DCM, and IPA, recirculating over 70% of solvents in each batch. By switching to lower temperature routes and more efficient reactors, we curtail waste generation and reduce our CO2 footprint. We’ve adopted packaging materials that meet customer requests for sustainability, using recyclable HDPE and reducing single-use plastics wherever we can without compromising product safety.
Supply chain interruptions and raw material volatility impact all of us. We’ve built redundancy into sourcing precursors, run real-time QA on all incoming raw materials, and partner with logistically stable carriers to tighten lead times. By controlling each critical manufacturing step, we don’t allow the quality slip-ups common among resellers or repackers with no manufacturing oversight.
Direct relationships with end-users grant us an open window into real-world application issues—problems that rarely show up in basic specification sheets. Consulting with customers, we’ve learned that high-throughput labs often battle static or clumping in powdered amino acid products. To address this, we install anti-caking steps pre-packaging and test every lot for flow properties as well as content uniformity. In the event that a user encounters a unique application or needs further customization (such as isotopically labeled lysine for metabolic studies), we have both the capacity and agility to step in with a tailored solution.
Early-stage developers sometimes underestimate the need for technical support when transitioning from a few milligrams to tens of grams in batch size. Raw materials can behave unpredictably, and minor process tweaks become critical at larger scale. We bridge this gap by maintaining a technical applications support desk staffed with synthetic chemists who have run their own pilot plant campaigns, allowing for grounded advice—not scripted, hands-off responses.
No manufacturing run is ever perfect out of the gate. We encourage feedback loops with our major customers, regularly updating manufacturing documentation and process parameters to reflect findings from process deviations or unplanned analytical results. This constant cycle of review and improvement helps ensure our Fmoc-Lys-OH continues to perform beyond baseline specifications. Our documentation updates and lot trend analyses are shared with clients running clinical-stage trials or process validation, avoiding mismatches in analytical expectations.
To allow for easier troubleshooting, batch-specific certificates document every analytical finding, including micro-level impurity profiles and stability test outcomes. We refresh stability studies annually so users operating at extended storage conditions—like those in large pharma and government research settings—can plan inventory management confidently.
Looking ahead, we see Fmoc-Lys-OH continuing to stake out territory in emerging therapeutic fields. Conjugated peptide drugs, radiolabeled tracers, and new delivery vectors all demand amino acid building blocks with dual protection and standout purity. Industry feedback backs up that switching to our product line correlates with reduced OOS incidents, higher clean-up yields, and smoother scaling from benchtop to pilot plant.
High-purity Fmoc-Lys-OH is more than just a synthesized intermediate—it’s a decision point for anyone building value into peptide chemistry projects. Our investment in large-scale equipment, exacting purification, and relentless QC delivers a differentiator customers see in their own analytics and process outcomes. For decades, we’ve made it a point to put our name only behind batches that meet our stated goals for integrity, consistency, and technical performance.
To those driving innovation in drug development, diagnostics, or bioconjugate studies, every amino acid matters. From our vantage point as dedicated producers, trust in raw materials forms the bedrock of successful, reproducible chemistry—especially when projects scale up or move closer to regulatory review. Fmoc-Lys-OH delivers the balanced protection, purity, and process reliability needed at the sharpest edges of peptide research and production. By staying hands-on, listening closely to user needs, and refusing to compromise on analytical scrutiny, we deliver more than just a chemical; we provide ongoing confidence for scientists and manufacturers alike.