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HS Code |
817414 |
| Chemical Name | Tert-Butoxycarbonylamino-Phenyl-Acetic Acid |
| Molecular Formula | C13H17NO4 |
| Appearance | White to off-white solid |
| Melting Point | 120-125°C |
| Solubility | Soluble in DMSO, methanol, and ethanol |
| Cas Number | 18148-48-6 |
| Purity | Typically >98% |
| Storage Temperature | Store at 2-8°C |
| Smiles | CC(C)(C)OC(=O)NC(C1=CC=CC=C1)C(=O)O |
| Inchi | InChI=1S/C13H17NO4/c1-13(2,3)18-12(17)14-10(11(15)16)9-7-5-4-6-8-9/h4-8,10H,1-3H3,(H,14,17)(H,15,16) |
| Usage | Amino acid/peptide synthesis intermediate |
As an accredited Tert-Butoxycarbonylamino-Phenyl-Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 25 grams, sealed with a red screw cap; labeled with chemical name, hazard pictograms, and batch information. |
| Shipping | Tert-Butoxycarbonylamino-Phenyl-Acetic Acid is typically shipped in sealed, airtight containers to prevent moisture absorption and degradation. It should be packed in accordance with chemical safety standards, labeled appropriately, and transported at ambient temperature. Ensure compliance with local regulations and safety data sheet recommendations for secure and compliant shipping. |
| Storage | Tert-Butoxycarbonylamino-Phenyl-Acetic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong acids and bases. It should be kept at room temperature (15–25°C). Minimize moisture exposure and avoid heat sources. Ensure proper labeling and follow standard laboratory safety protocols during handling and storage. |
Applications of Tert-Butoxycarbonylamino-Phenyl-Acetic Acid in Industrial ManufacturingAs a specialist manufacturer of Tert-Butoxycarbonylamino-Phenyl-Acetic Acid, we supply this advanced intermediate to key downstream sectors where its molecular structure enables precise control in multi-step syntheses. Below we outline major real-world application scenarios, presenting actionable data on compliance, formulation, process integration, and resulting end products to support specification decisions for professional buyers and technical formulators. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) SynthesisTert-Butoxycarbonylamino-Phenyl-Acetic Acid serves as a protected amino acid building block in the synthesis of pharmaceuticals, particularly in the step-wise assembly of peptide and peptidomimetic drug substances. Its tert-butoxycarbonyl (Boc) protecting group enhances selectivity and yields during key coupling reactions performed under controlled cGMP conditions, and its phenylacetic acid moiety supports the creation of API scaffolds for CNS-active, anti-inflammatory, and oncology drugs. This intermediate enters at the protected amino acid combination stage, ensuring effective protection/deprotection sequences aligned with target compound synthesis. Industry compliance standards
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2. Peptide Synthesis Reagents for Custom Peptide ManufacturingContract peptide manufacturers incorporate Tert-Butoxycarbonylamino-Phenyl-Acetic Acid as a protected amino acid analog in solid-phase and solution-phase peptide synthesis. The material’s stability during repetitive deprotection and coupling cycles is critical for chain elongation of therapeutic peptides, diagnostic probes, and enzyme substrates. Its application comes before resin loading or as a specific chain-terminating or branching residue, contributing to high-fidelity sequence assembly and contaminant control. Industry compliance standards
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3. Fine Chemical Synthesis for Advanced Organic IntermediatesProducers of specialty organic molecules, including fine chemical and custom synthesis houses, designate Tert-Butoxycarbonylamino-Phenyl-Acetic Acid as a reliable protected amine source in the formation of advanced intermediates for agrochemicals, complex ligands, or specialty polymer additives. The Boc-protected group stabilizes the molecular fragment against side reactions in multi-step synthetic schemes, facilitating selective functionalization and downstream conversion. Industry compliance standards
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4. Research-Grade Raw Material for Bioconjugation and Life Science KitsLife science and diagnostic kit manufacturers source this Boc-protected phenylacetic acid as a critical handle for bioconjugation protocols, particularly in the site-specific functionalization of proteins, oligonucleotides, and synthetic markers. Its structure allows for temporary amine protection during the preparation of linker molecules, fluorophore labels, or affinity tags, indispensable for users developing research reagents or conjugated assay components. Industry compliance standards
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Every day on our manufacturing floor, Tert-Butoxycarbonylamino-Phenyl-Acetic Acid stands as a workhorse in amino acid derivatization and peptide synthesis labs. This compound, often referenced by its abbreviation Boc-phenylglycine or by its molecular structure—where a tert-butoxycarbonyl (Boc) group protects the amino end—delivers in both performance and consistency. Years of producing and refining Boc-protected amino acids have solidified its role in building complex molecules that demand both selectivity and ease of deprotection.
We craft Tert-Butoxycarbonylamino-Phenyl-Acetic Acid to support rigorous synthetic needs. Our process uses clean, reproducible steps and our experience navigating the nuanced requirements of pharmaceutical and research applications taught us the importance of trace-level purity. Chemists gravitate toward this product when seeking a foundation that resists racemization and delivers well-characterized intermediates. Whether handling large process batches or specialty orders, we see how the use of a Boc group often means an easier, more dependable synthetic journey.
As manufacturers, we provide material produced under controlled parameters, offering specification grades that suit both medicinal chemistry labs and kilo-scale synthesis campaigns. The white solid, with its crystalline form, responds predictably to bench protocols. Our operators handle it confidently—moisture and thermal stability reduce worries about early decomposition or the need for elaborate precautions. Solubility in common organic solvents such as dichloromethane or ethyl acetate ensures that downstream reactions progress without bottlenecks.
On a practical level, we see the positive impact of a dependable melting point, batch-to-batch consistency, and full compliance with established purity benchmarks. Every lot released from our facility must meet internal spectroscopic (NMR and IR) and chromatographic standards. By controlling the upstream chemistries of Boc-protected phenylglycine, fewer surprises arise at purification or further derivatization stages. For many clients, the detailed certificate of analysis reassures, but for us, it's the visible outcome of years spent optimizing every step.
Experience has shown us that the Boc-protected variation serves a specific kind of chemistry. Free phenylglycine, without protection, often undergoes unwanted side reactions. Attaching the Boc group through our standardized method shields the amino functionality, permitting selective transformation at the carboxyl group or on the aromatic ring. During multi-step synthesis, these features cut down on byproduct formation, allowing for more predictable yields and easier workup.
Deprotection techniques further emphasize its versatility. A mild acid such as trifluoroacetic acid strips the Boc group cleanly, without damaging sensitive motifs elsewhere in the molecule. Chemists who have spent hours navigating stubborn protecting groups appreciate the straightforward nature of Boc chemistry—minimal side reactions, fewer purification headaches, and overall better process economy. The result reflects in cleaner intermediates, lower waste, and increased confidence that processes scale up with ease.
Consistent results stem from rigorous controls: our facility uses validated cleaning procedures and in-process testing protocols tuned specifically for protected amino acids. Every finished batch passes through a sequence of tests targeting color, clarity, melting point, and contaminant limits. Our own operators endorse using this material internally whenever challenging syntheses demand reliable reactivity profiles.
Clients often request insights on solvent compatibility and reaction sequences; our technical team draws from in‑house trials and feedback from collaborative development programs. Acumen sharpened through real-world manufacturing keeps us grounded in practical solutions—not just promising paper specs. We know that trace water content, batch homogeneity, and packing density matter just as much as headline purity. Years of handling this product showed us that small details—such as storage at ambient conditions and freedom from caking—help chemists move efficiently from weighing to reaction setup.
Experience divides products in the same class. Tert-Butoxycarbonylamino-Phenyl-Acetic Acid stands out because it delivers high stability during storage and manipulation. Unprotected phenylglycine, or products shielded by less robust groups, often give inconsistent release, side-chain modifications, or unwanted polymer formation. By contrast, our Boc derivative handles atmospheric moisture well and remains inert under neutral or basic conditions.
Other protecting groups, like the benzyloxycarbonyl (Cbz) or fluorenylmethyloxycarbonyl (Fmoc), do find use in specialized segments. Over the years we compared these options through side-by-side evaluations. Boc chemistry wins out especially where mild acid deprotection is desired. Laboratories running solid-phase peptide synthesis or assembling combinatorial libraries often cite Boc derivatives for the predictable deprotection timing and simple downstream treatment. Meanwhile, Fmoc-based products cater more to base-cleavable applications, showing less appeal for classical solution-phase chemistry where acid-lability speeds up the workflow.
We draw on decades spent troubleshooting, tuning, and applying this compound. Tests on incoming raw materials help exclude batch-to-batch drift. Internal and customer-driven investigations occasionally raise the bar: requests for heavy-metal screening, microbial limits, or stricter storage protocols rarely catch us off guard. We steadily expanded our analytical toolkit to include HPLC, qNMR, and finely calibrated moisture assays to provide transparent, objective data to partners.
During peer-to-peer conversations at technical conferences or industry forums, we share our findings in terms of shelf-life, packaging improvements, and resistance to degradation under light or mild thermal exposure. These came not from theoretical speculation, but from lived operational challenges and iterative improvement. We find that reporting actual shelf stability, not just the theoretical maximum, supports purchasing and inventory decisions for both large pharmaceutical customers and small research groups.
From the factory floor, usage patterns highlight that most Boc-phenylglycine heads into peptide coupling streams. Research chemists constructing penicillin analogues, or those in early-stage biologic drug candidates, count on Tert-Butoxycarbonylamino-Phenyl-Acetic Acid as a key intermediate. Feedback loops with users led us to focus on prompt lot release, batch reservation for scale-up, and minimizing cross-contamination risk.
Scale-up chemists depend on predictable performance when moving from milligrams to kilograms. Our facilities accommodate pilot-scale processes, using closed handling and monitored addition steps. We tuned drying and milling methods to boost handling ease, as experience showed that fine particle control lowers loss and speeds up transfer. That attention to detail goes well beyond listing physical properties; it comes from watching real teams solve the day-to-day obstacles of multi-step synthesis campaigns.
A major pharmaceutical partner running long synthetic routes once shared their pain points: inconsistent release characteristics, variable particle sizes, and sensitivity to seasonal humidity swings from previous suppliers. They trialed our material, tested against severe in-process controls, and found out that robust packaging and standardized milling slashed time lost to sieving, rehomogenization, and waste. Over several campaigns, their need for rework dropped, and their bulk yields went up. Those lessons shaped our continuous improvement pathway—solutions built on what real users require, not just what catalogs promise.
Operating as a direct chemical manufacturer means strong accountability for every technical claim. Our material passes scrutiny under Good Manufacturing Practices where required, and our archival records allow full trace-back to origin. Third-party audits check our batch history and in-process controls. Product stewardship remains a daily reality—documented cleaning, careful raw material qualification, trend tracking, and continuous hazard review help avoid deviations and keep users out of regulatory pitfalls.
We participate in industry roundtables that shape purity thresholds and analytical reference points. Regular updates help keep us—and our customers—in step with evolving standards for elemental impurities and residual solvents. Site inspectors who walk our plant gain full access to supporting data, from supplier audits to batch sample logs. Regulatory trust is not about paperwork volume, but about the totality of lived competence. The value in a well-made Boc-protected amino acid shows when process records, certificates, and in-lab tests tell the same story.
Handling bulk chemical solids seems simple—but decades of manufacturing experience reveal the pitfalls waiting in suboptimal materials. Packed in moisture-resistant, tamper-evident drums, our Tert-Butoxycarbonylamino-Phenyl-Acetic Acid ships out with minimum transit loss and without hardening or bridging. Forklifts and warehouse teams appreciate that our packaging is robust enough for re-stacking, while production chemists note the lack of fines, dust, or caking when charging into reactors.
Internal record-keeping—tracking everything from the point of release to final shipment—feeds back into quality improvement. Even seemingly minor changes, like adjusting liner gauge or pallet height, can ripple forward into ease of stock rotation, reduced cross-contamination, and fewer picking errors. These are not theoretical benefits but the daily experience of a team that knows how each operational handoff affects the next.
Consistent particle size also proves its value during solution preparation: dissolving 1 kilogram for a 100-liter batch proceeds in predictable times, with minimal swirl or undissolved residue. Our lab partners call out the contrast to less-refined alternatives, which leave unsightly clumps or force the use of co-solvents not wanted in downstream processing. Over long projects, those small advantages add up—higher yield, faster turnarounds, less time lost to troubleshooting.
We avoid marketing gloss—our technical team spends real time on the production line and in customer pilot runs. If a batch raises spectroscopic anomalies or fails an established threshold, it never leaves our dock. Early in our production history, we encountered a scenario where a late-stage impurity from incomplete Boc installation had crept into a portion of material. That experience pushed us to institute redundant in-process monitoring, catching issues before batch closure rather than relying solely on finished-goods checks.
On a process-side challenge, customers sometimes report frustration about foaming or slow dissolution during scale-up. That prompted us to keep particle size within tighter bands and document agitation protocols to minimize surprises. Communication with clients—sharing what works, what doesn’t, and what to expect—forms the backbone of trusted supplier relationships. The key, we learned, is adaptability born from both direct feedback and self-driven audits.
Ongoing advances in synthetic biology, small molecule drugs, and advanced material platforms continually reshape demand for protected phenylglycine derivatives. We see the product traveling across geographies, crossing into academic, biotech, and major pharmaceutical settings. Each field brings unique constraints: research units favor small but frequent orders with quick certificate turnaround; commercial plants prioritize bulk, stable deliveries on tight schedules.
Feedback streams directly into production decisions. Beyond classic peptide syntheses, some partners push exploratory work into new chiral scaffolds or as part of combinatorial build-outs. We field technical questions daily—from how the Boc group stands up to alternate solvents, to which downstream steps benefit or suffer if using Boc versus Cbz or Fmoc variants. These exchanges drive practical innovation, not just sales volume.
Recent advances in green chemistry and continuous manufacturing led us to review the full lifecycle of Boc-phenylglycine in process design. Where solvents can recycle, processes close loop, and waste minimizes, we adapt both analytical and bulk production controls. Our plant teams test new approaches on the bench before rolling them out at scale, making changes only after confirming performance does not suffer.
Our viewpoint, honed over years, shows that producing fine chemicals is not a transactional affair. Years of repeat business with major laboratories, contract manufacturers, and academic innovators underscore how Boc-protected phenylglycine endures as a staple of method development. Longstanding users expect continuity—not just in product, but in service and technical support. Experience keeps us wary of chasing every new trend; instead, we focus on strengthening baseline reliability.
Close collaboration with users led to process tweaks, better logistics, and user-friendly technical documentation. Soapbox marketing cannot replace real answers to technical support needs—such as how to transfer, dissolve, and apply Boc-protected intermediates under variable plant conditions or shifting regulatory winds. Our goal remains to get real chemists closer to their targets, while absorbing at least part of the unavoidable uncertainty inherent in modern multi-step synthesis.
Looking ahead, demand for Tert-Butoxycarbonylamino-Phenyl-Acetic Acid seems resilient, fueled by its utility in bespoke peptide and small-molecule pipelines. As research and process development converge on leaner, cleaner, and sustainably sourced materials, pressure rises for transparent supply chains and validated manufacturing records. Our commitment to openness and technical partnership gives us a front-row seat to evolving expectations.
We intend to keep drawing on hard-won experience and in-person know-how, blending it with sound scientific evidence and emerging process needs. Whether stabilizing supply lines, supporting regulatory filings, or helping troubleshoot yet another complex synthetic pathway, our approach stays rooted in the fundamentals that make chemical manufacturing a craft: attention to real-world detail, teamwork with users, and a drive for continuous improvement anchored in both practice and proof. Through all these efforts, Tert-Butoxycarbonylamino-Phenyl-Acetic Acid remains not just a catalog item, but a tested ally in the hands of working chemists worldwide.