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HS Code |
576542 |
| Product Name | Boc-4-Amino-L-Phenylalanine |
| Cas Number | 72336-38-6 |
| Molecular Formula | C14H20N2O4 |
| Molecular Weight | 280.32 |
| Appearance | White to off-white powder |
| Purity | Typically ≥98% |
| Melting Point | 106-110°C |
| Solubility | Soluble in DMSO, methanol |
| Storage Temperature | 2-8°C |
| Protecting Group | Boc (tert-butoxycarbonyl) |
| Chirality | L-isomer |
| Synonyms | N-Boc-4-amino-L-phenylalanine |
As an accredited Boc-4-Amino-L-Phenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Boc-4-Amino-L-Phenylalanine is supplied in a sealed amber glass vial, 5 grams, with a tamper-evident cap and clear labeling. |
| Shipping | **Shipping for Boc-4-Amino-L-Phenylalanine:** This chemical is securely packaged in sealed containers to prevent exposure to moisture and contaminants. It is shipped at ambient temperature under standard, non-hazardous chemical guidelines. Accompanying documentation includes safety data sheets. Expedited and international shipping options are available to ensure timely and safe delivery. |
| Storage | Boc-4-Amino-L-Phenylalanine should be stored in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerated conditions). Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Proper storage helps maintain the compound's stability and purity for laboratory use. Always follow relevant safety and handling guidelines. |
Applications of Boc-4-Amino-L-Phenylalanine in Industrial ManufacturingBoc-4-Amino-L-Phenylalanine serves as a key protected amino acid intermediate widely utilized in high-value peptide synthesis workflows and pharmaceutical development. As a direct manufacturer, we work closely with industrial partners to support large-scale applications where process reliability and consistency are crucial. Below we detail core real-world downstream applications, providing industry-specific compliance, formulation practice, process integration, and typical finished goods. 1. Peptide Drug Active Pharmaceutical Ingredient (API) SynthesisPeptide pharmaceutical manufacturers incorporate Boc-4-Amino-L-Phenylalanine as a protected building block in the solid-phase synthesis of linear and cyclic peptide APIs for use in metabolic, oncology, and cardiovascular therapeutics. The raw material ensures strict control of stereochemistry and selective deprotection during elongation cycles, supporting cGMP batch records with minimized impurities. Production requires traceable documentation for every input, and the ratio depends on peptide sequence design. Industry compliance standards
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2. Diagnostic Peptide Reagent ProductionManufacturers of immunoassay kits and biosensor calibration standards use Boc-4-Amino-L-Phenylalanine for precision assembly of peptide sequences with terminal modifications necessary for bioconjugation. The material’s purity and absolute configuration are crucial for consistent batch-to-batch reactivity in downstream diagnostic applications, where lot validation and traceability support ISO requirements for critical reagents. Industry compliance standards
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3. Custom Peptide Manufacturing for Preclinical ResearchCROs and specialized life science suppliers demand Boc-4-Amino-L-Phenylalanine when assembling bespoke peptides for use in drug screening, receptor binding studies, and molecular probe development. Clean protection of the amino function avoids side reactions, which is especially critical for multiparameter library synthesis and enables iterative contract batch production for global R&D pipelines. Industry compliance standards
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4. Intermediates for Chiral Specialty Chemical SynthesisProducers of chiral intermediates and fine chemicals include Boc-4-Amino-L-Phenylalanine as a resolved, protected starting material in multi-step syntheses targeting pharmaceutical scaffolds and specialty amines. The distinct configuration and Boc group stability offer an advantage in protecting-group strategies during hydrogenation, acylation, or coupling workflows essential for high-purity intermediate output. Industry compliance standards
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5. Bioconjugation Linker Construction for Antibody-Drug Conjugates (ADCs)CDMOs and biotech firms apply Boc-4-Amino-L-Phenylalanine during design of cleavable linker units for ADCs, where the orthogonally protected amino moiety allows for tailored site-selective conjugation to antibodies. The material’s integrity directly affects linker-payload consistency and downstream purification profile, meeting strict bioprocess accountability. Industry compliance standards
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In our plant, the journey from raw amino acid through to refined Boc-4-Amino-L-Phenylalanine isn’t just a batch process—it’s a daily exercise in precision and trust. Each step, from the controlled addition of t-butyloxycarbonyl to the purification that clears residual by-products, shapes a product we know researchers rely on to protect their projects against uncertainty. Boc-4-Amino-L-Phenylalanine, our signature protected derivative of 4-amino-L-phenylalanine, enters the market meeting strict standards for stereochemical integrity, stability, and easy solubility, delivering not only a reagent but a trusted tool for peptide synthesis and pharmaceutical development.
We never treat this intermediate as a standardized good. Every lot receives batch-specific checks not just for purity by HPLC but for elemental consistency, chiral purity, and residual solvent traces. Many times, customers ask what really differentiates Boc-4-Amino-L-Phenylalanine from similar protected amino acids. The answer isn’t only in the analytical readings—though we keep the optical rotation, specific purity, and water content to tight tolerances. The value comes from how predictably it performs across peptide couplings, without unplanned cleavage or racemization, supporting consistent chain extension even under tough scale-up or solid-phase conditions.
Our experience suggests most scientists choose Boc-4-Amino-L-Phenylalanine when they work on segments that need both side-chain and N-terminal selectivity. The Boc (tert-butyloxycarbonyl) group hangs onto the amino function through tough coupling steps and caustic solvents but still releases cleanly under acid deprotection. With each lot, we guarantee a single isomer: all L-stereochemistry, all verified by chiral HPLC and polarimetry. We manufacture with a molecular formula of C14H20N2O4, molar mass checked at 280.32, and we confirm both IR and NMR signatures as part of release criteria.
We stick with a solid-white crystalline powder—clumping, off-coloring, or softening below room temperature flag immediate investigation. Loss on drying below 0.50% avoids solvent retention, and heavy metal content stays well below permitted limits. By holding water soluble impurities to below 0.1%, we see fewer complications downstream, particularly in polymer-bound systems or when optimizing stepwise peptide assembly.
When our teams prepare a batch, we do not cut corners between reaction efficiency and product workup. We have learned over many years: over-drying or overheating can compromise both texture and subsequent reactivity, affecting total yield and engineer confidence. Each operator cross-checks against verified reference spectra and microanalytical data—no deviation moves forward. Where possible, we test for traces of related impurities that can slip unnoticed, like dicyclohexylurea, which might escape crude filtering if not watched closely. Our trust in Boc-4-Amino-L-Phenylalanine reflects this first-hand care.
Boc-4-Amino-L-Phenylalanine does more than bridge the gap between raw amino chemistry and pure, extended peptides. We see it often used in the design of biologically active oligopeptides, where a para-amino phenyl ring offers the kind of functional diversity that opens up point attachment for fluorophores, other side chain conjugation, or even cross-linking strategies. Its popularity comes from sturdy performance and the peace of mind researchers have in each batch.
Compared with standard Boc-protected amino acids, the presence of the para-amino substituent gives more flexibility for orthogonal protecting approaches. Our customers report greater convenience in sequential modifications, since the Boc group stays put through neutral/basic treatments, then can be selectively removed in TFA without affecting most side chain protections. When building up sequence libraries, or introducing labels, the difference between a stable Boc group and a less robust substitute translates directly to real-world project savings.
Another significant aspect involves automated solid-phase synthesis. Automated synthesizers demand a product that flows well, dissolves predictably, and delivers complete coupling across multiple cycles. Their reliability, and ultimately the reproducibility of pharmaceutical prototypes, depends on consistent lot-to-lot Cox-4-Amino-L-Phenylalanine characteristics. We run practical, application-focused tests on each release to verify reaction kinetics and coupling efficiency. Not every supplier can say this or back it up with real, published data. This is where long-term customer feedback matters: we routinely adopt suggestions from laboratory partners so each lot reflects a shared commitment to continuous improvement.
There is no such thing as a “problem-free” protected amino acid. Even the best materials challenge users in ways that specifications cannot predict. Sometimes, instability in unrelated reagents causes unexpected deprotection or degradation. Sometimes a new salt form or additive interacts with the para-amino group. These experiences have taught our technical support teams to look beyond our own analysis and listen to feedback from researchers, especially those running overnight solid-phase cycles or multi-step, multi-day solution-phase protocols.
Everyone on our production line has seen how solvents and resin choices play unexpectedly large roles in the performance of Boc-4-Amino-L-Phenylalanine. We advise using dry DMF, DCM, or acetonitrile for best results; using water-prone systems can trigger micro-aggregation or solubility drops that do not appear in bench-scale runs. The physical form we ship—never pressed into tablets, never pelletized, always loose crystalline powder—reflects years of direct feedback and hands-on troubleshooting.
Customers sometimes report minor foaming or sticking during scale-up. These issues trace back not to the base amino acid, but to subtle moisture uptake or slow-release fines from older sample stock. Here’s where attention to shelf-life and proper container sealing matters. Out of direct humidity and kept in properly sealed, low-static containers, Boc-4-Amino-L-Phenylalanine retains its free-flowing, easy-dispensing character for far longer than most anticipate. We encourage storing at 2–8°C to extend shelf life, but never so cold as to risk condensation on reopening.
Chemists debating between Boc and alternative protections always weigh trade-offs between acid lability, ease of removal, compatibility with side-chain modifications, and risk of stereochemical drift. Our history with Boc-4-Amino-L-Phenylalanine shows that the Boc group, while robust through mild base and neutral conditions, comes off quickly and cleanly with acid, without risk of cleaving valuable side chains or triggering unwanted cyclizations. Compared to Fmoc or other orthogonal handles, the Boc group enables direct acidolysis without additional deprotection steps.
In peptide synthesis, especially with complex sequences, small changes in reactivity yield dramatic differences in final product integrity. Boc-4-Amino-L-Phenylalanine, owing to the para-amino substitution, serves especially well in building blocks for custom antigenic peptides, drug candidates, or targeted probes. Its powder readily dissolves in organic media favored during automated solid-phase processes, and resists the kind of hydrolysis problems linked to certain other protection schemes.
When switching from Fmoc-protected analogues, researchers note differences in deprotection conditions, side-reactivity, and ease of handling. While Fmoc versions give base-labile protection, the Boc approach matches better with acidolytic workflows and leaves the side-chain para-amino group untouched for further manipulation. From our experience, this combination frequently reduces the number of steps needed in library construction, accelerating screening and structure-activity relationship projects.
Looking across diverse customer groups—academic researchers, contract peptide manufacturers, biotech startups—we’ve observed clear patterns in how Boc-4-Amino-L-Phenylalanine improves efficiency and reduces costs. In academic labs, teams appreciate having a reagent that doesn’t drop out of solution or form byproduct junk at coupling or deprotection. Time after time, minor process tweaks on our end translate to big productivity gains on theirs.
In scaled industrial settings, the small variables add up. Even tiny inconsistencies in the batch cause downstream headaches during analytical purification, HPLC, or crystallization. We keep heavy oversight on every release, running parallel process mimicry to give customers confidence batches won’t shift from test lot to full-scale use.
Some users need adaptation to specific applications—say, non-traditional protection strategies, or coupling with nonproteinogenic units. These aren’t “specification” issues, but realities of research work. We welcome feedback and routinely collaborate with customers who push the boundaries of peptide chemistry, integrating their hands-on observations with our process optimizations. This style of manufacturer-researcher partnership benefits our process just as much as it benefits the end user.
Traditional problems like needle clogging in synthesis robots, crystallization out in storage, or unexpected UV absorption levels can often be traced right back to micro-contaminants, water content, or subtle differences in crystalline form. We believe maintaining a conversation with end users about these issues is a core manufacturer’s duty. Boc-4-Amino-L-Phenylalanine can’t realize its full potential without both sides—generator and user—constantly improving and sharing practical notes.
Our plant takes pride in the fact that repeated users of Boc-4-Amino-L-Phenylalanine comment not on abstract purity numbers but on batch reproducibility and ease of handling. Many fine chemicals can claim high performance; few deliver the same every time. We keep a close eye on how even trace levels of unrelated amino acids or solvent residues slip through, shaping remediation protocols based on root-cause analysis, instead of just reacting after the fact.
Batch records, operator logs, and mid-process analytics frame our commitment to transparency. These aren’t marketing phrases; they are the daily record of risk reduction at the center of a manufacturer’s credibility. Each shipment includes full analytics not because it’s required, but because our partners often need independent confirmation or third-party validation at regulatory or scale-up milestones.
Where synthesis turns up new incompatibilities, we plug those lessons right back into our process. We believe real experience solves more problems than any datasheet. It’s not unusual for a user to want custom-scale packaging, pre-tested dilution, or consultation on process tweaks. Our team’s direct exposure to these varied requests keeps us grounded and focused on real value.
Many technical challenges with Boc-4-Amino-L-Phenylalanine relate less to its own chemistry than to system-wide implementation. If environmental controls slip or solvent handling varies between runs, performance can nudge outside expected lines. Years of supporting remote customers have taught us to anticipate issues related to moisture intrusion, container design, and even vial static charges—a real nuisance in cold, dry seasons. These “minor” issues account for a surprising fraction of call-outs we receive.
Packing in moisture-resistant, static-dissipating bottles and running stability trials under varying humidity conditions, we have fine-tuned advice for storage and handling. While the crystal form we manufacture presents minimal dust or particulate load, even the best product loses performance if handled with damp utensils or left unsealed after measurement. We recommend simple, clear procedures for transfer and re-cap, instructions developed through day-to-day support cases.
Analytical labs, especially those preparing for preclinical QA or multi-sequence custom libraries, often find subtle inconsistencies when using products sourced from multiple suppliers. That’s why we let users trace every vial or package back to production log and in-process sample. This minimizes surprise out-of-spec results. In some cases, collaborating labs have returned partially used material so our technical group can run parallel analysis and break down nuanced performance drifts. That openness drives many of our minor (and sometimes major) formulation changes.
The practical knowledge we’ve collected about Boc-4-Amino-L-Phenylalanine, not just as a chemical but as a working lab tool, flows back into refining its physical and chemical characteristics. By sharing practical use cases with customers and gathering their in-situ feedback, we gradually shift batch processing norms to favor not only purity, but direct reactivity and stability in diverse or shifting conditions.
Users ask for more than off-the-shelf perfection. Some want custom sieving or particle size grading to match semiautomatic dispensers, others need test series to benchmark against new coupling reagents. Because peptide chemistry evolves with each new target, we commit to ongoing dialogue with chemists on the front lines. Our aim is always to lower the risk of synthetic hiccups that eat into time and budget.
Projects don’t always run at room temperature, nor do starting solvents always match published standards. Recognizing exceptions has led us to develop support cases tailored to the real-world bench: “What happens in a humid climate?” or “How does this batch react with my custom resin?” These lived experiences build trust not with promises, but with direct, tested improvement.
We refuse to rest on analytical numbers alone. In today’s landscape, more researchers care about batch-to-batch continuity and direct support than about abstract specification lists. This approach has made our Boc-4-Amino-L-Phenylalanine not just a catalog entry, but a partner in building the future of custom peptides, bioactive molecules, and novel tools in biomedical research.
Every kilogram leaves our facility with the memory of the men and women who measured, checked, adjusted, and released it—not just as a chemical, but as a catalyst for discovery.