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HS Code |
749117 |
| Product Name | N-Boc-L-Phenylalaninol |
| Iupac Name | (S)-tert-butyl (2-hydroxy-3-phenylpropyl)carbamate |
| Molecular Formula | C14H21NO3 |
| Molecular Weight | 251.32 g/mol |
| Cas Number | 110117-83-4 |
| Appearance | White to off-white solid |
| Melting Point | 62-66°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like dichloromethane, methanol |
| Optical Rotation | [α]D20 +21° (c 1, MeOH) |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited N-Boc-L-Phenylalaninol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-Boc-L-Phenylalaninol, 5 grams, is supplied in a sealed amber glass bottle with a secure screw cap and tamper-evident label. |
| Shipping | N-Boc-L-Phenylalaninol is shipped in tightly sealed, chemically resistant containers under cool, dry conditions to prevent moisture and contamination. Packaging complies with relevant regulations for chemical transport, including labeling for laboratory use only. Standard shipping avoids extreme temperatures, and all documentation ensures traceability and safe handling upon receipt. |
| Storage | N-Boc-L-Phenylalaninol should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place at 2–8°C (refrigerator temperature). Avoid exposure to air and incompatible substances such as strong acids, bases, or oxidizing agents. Ensure proper labeling, and store away from food and drink areas in a designated chemical storage cabinet. |
Applications of N-Boc-L-Phenylalaninol in Industrial ManufacturingN-Boc-L-Phenylalaninol is a valuable chiral intermediate widely adopted in multiple fine chemical and pharmaceutical production streams due to its stable protecting group and defined stereochemistry. As a direct manufacturer with in-house process control and rigorous sourcing, we support downstream partners with reliable, high-purity supply for specialized transformations. Below, we detail its main industrial applications, focusing on compliant integration into actual commercial manufacturing lines. 1. Active Pharmaceutical Ingredient (API) Chiral SynthesisLarge-scale API manufacturers incorporate this intermediate for the enantioselective production of non-peptide and peptide-mimetic therapeutic agents, utilizing its chiral alcohol moiety during amide coupling and reductive amination steps. The Boc-protected group protects the amine functionality through multi-step synthetic routes, supporting batch synthesis under GMP-compliant environments. Industry compliance standards
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2. Asymmetric Catalyst Ligand SynthesisManufacturers of proprietary asymmetric catalysts employ N-Boc-protected phenylalaninol as a core building block for chiral ligand frameworks. Its defined stereochemistry imparts selectivity within homogeneous or heterogeneous catalyst assemblies, typically for use in hydrogenation, epoxidation, or cyclopropanation chemistry. Industry compliance standards
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3. Peptide Analogue Intermediate ManufacturingProducers of specialty peptide analogues and modified amino acid blocks utilize the Boc-protected phenylalaninol to introduce chiral alcohol termini or as a precursor to further functionalized residues. This approach supports synthesis of peptido-mimetic R&D tools used for structure-activity studies or injection into peptide backbone libraries for therapeutic screening. Industry compliance standards
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4. Fine Chemical Intermediate for Custom SynthesisCustom synthesis facilities and CDMOs incorporate Boc-phenylalaninol as a key intermediate in multi-step preparation of advanced organic compounds, especially for projects requiring unique chiral orientation and protected functional groups. Rigorous batch records, in-process analytical testing, and traceability accompany each production step in accordance with contract specifications. Industry compliance standards
Typical usage ratio
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In our production halls, each batch of N-Boc-L-Phenylalaninol passes through years of accumulated practical know-how, sharpened not just by textbooks but by decades spent at the interface of laboratory needs and scalable manufacturing. The product, also known as tert-Butyloxycarbonyl-L-phenylalaninol, holds a distinct place on our list for what it enables in the world of chiral chemistry and peptide synthesis. The effort poured into its consistent, reproducible manufacture continues to pay off as our partners in pharma and fine chemicals make advances in peptide and API development.
At the plant, it’s never just about “making a chemical”—it’s about controlling process details so minute changes won’t slip by. For N-Boc-L-Phenylalaninol, attention focuses on purity, batch lot uniformity, and absolute configuration. Customers trust us for consistent optical purity, and we achieve this through repeated hands-on analytical verification, not just reliance on historical batch data. It comes from understanding how solvents, temperatures, and purification procedures affect the final product and tightening each step to improve repeatability.
Operational safety catches our eye during every campaign: we focus on reducing worker risk, keeping operator exposure as low as possible, and handling intermediates with precautions developed from direct experience. Each production batch brings its own lessons about managing the exotherms from Boc protection, balancing throughput with gentle processing, and fine-tuning our chromatography and crystallization to weed out undesired isomers or trace byproducts.
Chemists come to us when their research projects demand not just any L-phenylalaninol derivative, but tight control over stereochemistry and protection. N-Boc-L-Phenylalaninol’s defining advantage lies in how it delivers the protected L-configuration in an alcohol form, which opens up key reactivity at the benzylic center without sacrificing stability during intermediate steps. The Boc group shields the amine, allowing tough coupling reactions or redox steps to proceed with minimal risk of side reactions at that sensitive site.
Its alcohol group is not only reactive, but extremely useful for selective further modification, bringing flexibility whether you’re building chains from the C-terminus or designing non-natural peptides. Peptide researchers see the value in controlling protecting groups. In our experience, the difference between a stalled reaction and a successful sequence often comes down to how the reagents present electron-withdrawing or donating effects, steric hindrance, and compatibility with common activating agents.
Through decades of feedback and hands-on process development, the major distinctions between N-Boc-L-Phenylalaninol and alternative building blocks crystalize around stability, ease of deprotection, and downstream reactivity. The Boc group generally stands out from Fmoc and Cbz for its balance when it comes to removing the protection under mild acidic conditions, avoiding extended exposure that can trigger side reactions that we all want to avoid in multi-step syntheses. Other protecting groups might force a tradeoff between stability and work-up time, but Boc has proved to be robust enough for most peptide coupling protocols without holding up the workflow when removal is needed later.
Some may opt for unprotected L-phenylalaninol or use methyl/ethyl esters; experience teaches that this route can cut corners only for the simplest chemistries. Once side-chain manipulations or more aggressive activating agents come onto the scene, these forms quickly run into roadblocks from unwanted reactivity at the amine. In contrast, N-Boc-L-Phenylalaninol keeps options open, letting teams fine-tune their synthesis strategies.
Structural analogues like N-Boc-L-phenylalanine differ in their reactivity profile, lacking the flexible hydroxyhandle of ‘-ol’ derivatives. This seemingly subtle difference can become the deciding factor in synthesis design, where the downstream functionality of the hydroxy group is desirable—whether for subsequent oxidation, cyclization, or conjugation steps. For this reason, our product functions as a linchpin in convergent strategies used in medicinal chemistry and bioconjugate development.
Working shoulder-to-shoulder with pharmaceutical development teams leaves us with a clear view of the critical role N-Boc-L-Phenylalaninol plays as a starting material or intermediate. It has supported our partners in streamlined synthesis of various non-proteinogenic amino acid derivatives, enabling construction of complex chiral drug scaffolds and enzyme inhibitors. Many modern peptide drugs incorporate sections derived from this compound; the stability of the Boc group helps researchers avoid unwanted racemization, which can upend a promising synthesis.
We’ve also seen rapid adoption in medicinal chemistry programs—teams seek to build libraries of small-molecule scaffolds where strict control of stereochemistry is paramount. The free alcohol function offers an anchor for further derivatization: phosphorylation, carbamate formation, or coupling with carboxylic acids. In the hands of a skilled team, this single building block opens a pathway to dozens of diversified analogues.
Specialty chemical makers demand rapid cycles from R&D to pilot scale without lengthy re-optimization steps. For them, the reproducibility and clean transition from lab to kilo-lab, made possible by our continuous investment in process tightness and scaleable chromatographic systems, matter just as much as the chemical’s theoretical uses. Stability during shipping, shelf life, and ease of handling come under close scrutiny as well—paralleled by our robust packaging and traceable internal logistics that cut losses from degradation or cross-contamination.
Quality boils down to tangible parameters, not marketing words. Spectrophotometric analysis tells the purity story, but in our workflow, we dig deeper with chiral HPLC and advanced NMR techniques to check that no off-isomer sneaks through. For every lot, we take hands-on confirmation steps: those extra controls catch minor process deviations before they become product variability headaches in a research lab. Raw material vetting, supplier audits, and in-house stress testing form the routine, not the exception. Few things stall innovation harder than a batch that fails baseline checks mid-campaign.
Operators run each process station with real-time data collection. We equip our staff with scalable, single-use tools where needed to knock down risk from cross-batch contamination. Each deviation notice triggers a team review, where we dig into root causes and apply corrective actions learned from real-world setbacks. It’s a cycle that pays back when our customers report robust assay results batch after batch. Over time, this investment in operational excellence shapes how our product performs outside our doors.
Years of producing N-Boc-L-Phenylalaninol at industrial scale have taught us the value of green process development—less waste sent for treatment equals less regulatory pressure, less community impact, and better margins all around. We select solvents and reagents not only for efficacy, but their life-cycle impact. Process integration lets us recover certain reagents, and whenever possible, shift off energy- or water-intensive steps. Case by case, we’ve reduced organic solvent use, phased out legacy wasteful methods, and substituted milder purification steps while maintaining product quality.
This outlook grows out of necessity: large-scale failures or repeated reprocessing eat into delivery timelines and environmental goals. As green chemistry expectations rise, our plant managers work directly with R&D to trial alternative reagents and anticipate regulatory shifts.
Some customers want support tracking and documenting the CO2 impact of sourced intermediates and asking for supplier transparency. We share our learning curves, lifecycle metrics, and audit data with those partners, making it easier for their compliance and sustainability teams downstream.
We listen when lab heads and synthetic chemists share feedback—sometimes it’s as concrete as an adjustment to dissolution rates, other times a tipoff about unexpected impurity under certain conditions. For instance, teams have flagged the need for better guidance on best storage practices for long-term stability, or minor degradant formation under high humidity. We’ve responded by changing packaging approaches and offering practical handling guides, informed by accelerated aging studies done at our own facilities.
University groups working on asymmetric synthesis projects occasionally struggle with reliable scale-up guidance. We provide direct access to our technical team for troubleshooting—after all, the limits of a process often come to light only beyond the 10-gram scale. Our formulation specialists help adapt lab protocols to kilo batches, preventing loss of precious starting material during transitions, based on real-world process data.
A recurring concern surrounds the interaction between the Boc group and more aggressive coupling agents. Some users encounter partial deprotection if standard conditions are not tightly controlled. Our process chemists, having walked through hundreds of reaction runs, recommend temperature, pH control, and suggest alternative protective strategies when needed—never offhand but based on fact-based troubleshooting from production lines.
No intermediate solves every synthetic challenge single-handedly. The Boc group’s benefits bring some sensitivity to acid exposure, so cold storage and protection from atmospheric moisture take on added importance. Our staff’s experience with minor hydrolysis or secondary impurities—especially in long-haul or warm-climate shipping—has led to new desiccant treatments and inspection steps before outgoing orders. We share recommended storage protocols with research teams up front, helping ward off shelf-life issues.
Some process routes push the product through oxidation or reduction environments unkind to either the alcohol or Boc group. Rather than leave chemists to trial-and-error, our teams collect hard-won knowledge about reaction condition compatibility and publish technical bulletins when we spot repeat issues. This information network becomes most useful when timelines are tight and batch wastage is unforgivable.
Handling hydroscopic reagents and sensitive intermediates as a manufacturer instructs us in the “real world” challenges: sometimes packaging or caps designed for bench scale can spell trouble in transit or when decanted on a busy production floor. We invest in packaging audits, tracking real-time customer feedback, and send out improved solutions that solve not only for lab convenience, but also for regulatory compliance—nipping issues before they reach researchers.
Trust builds through verifiable consistency, not only certification. Each drum and jar we prepare has batch record traceability, barcoding, and step-by-step documentation so users can track the chain from starting materials through process history. To many, this seems like mundane compliance—but in our experience, it means labs can pinpoint the source of an outlier or confidently meet downstream regulatory demands. We keep provenance records not only for external auditing, but to drive our own continual improvement; a feedback loop develops where we catch small signals before they grow into costly problems.
Partners in regulated sectors, especially those filing DMFs or new drug applications, need more than a certificate of analysis. We support dossier preparation with in-depth information on source chains, process controls, and analytic records. Our batch-level documentation has passed customer and third-party regulatory inspections—an achievement grounded in daily discipline, not just annual reviews.
Cost in high-purity N-Boc-L-Phenylalaninol production derives not simply from raw material inputs, but from overheads born of quality control, operator training, and facility up-time. Incremental product improvements—whether they touch filtration efficiency, in-process analytics, or packaging—return value by reducing out-of-spec final batches and turnaround between campaigns. We keep an eye on raw material price volatility, qualifying multiple suppliers and structuring contracts that support continuity even as the global landscape shifts.
We’ve weathered years when input material spikes or supply chain interruptions would have spelled disaster for unprepared operations. Process adaptation—substituting alternative precursors, stretching campaign sizes, and qualifying backup routes—keeps customers supplied when the market turns turbulent.
After years in this industry, patterns crystallize: the best advances happen when manufacturers partner with scientists from day one. Whether it’s troubleshooting a stalled coupling, scaling from bench to plant size, or integrating N-Boc-L-Phenylalaninol into novel synthetic designs, real progress depends on open dialogue and willingness to rethink established routines.
Our technical teams take pride in sharing application notes, cross-lab studies, and hands-on workshops with university and industrial groups. By making technical details transparent—sharing not just success stories but roadblocks encountered and solutions developed on the floor—everyone shortens the learning cycle. The bridges built through these exchanges fuel not only customer loyalty, but the evolution of process chemistry as a whole.
Standing at the convergence of green chemistry, automation, and increasingly complex regulatory environments, we see the expectation bar for intermediates rising each year. Our investment in analytical infrastructure, process traceability, and sustainable production keeps us ahead of shifting demands. Teams launching a new project, whether bench-scale or full GMP campaign, can draw on decades of hands-on expertise to avoid the pitfalls that slow down progress at the final mile.
From the first filtered liter to multi-ton flexible campaigns, our approach to N-Boc-L-Phenylalaninol stays rooted in meeting chemists at the point of real-world need. We’re committed to pushing the boundaries of what quality, transparency, and partnership mean in specialty chemical manufacturing—one batch at a time.