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HS Code |
820464 |
| Product Name | Fmoc-D-2-Nitrophenylalanine |
| Synonyms | Fmoc-D-o-Nitrophenylalanine |
| Cas Number | 204155-50-4 |
| Molecular Formula | C24H18N2O6 |
| Molecular Weight | 430.41 |
| Appearance | Yellow solid |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Protecting Group | Fmoc (9-Fluorenylmethyloxycarbonyl) |
| Chirality | D-isomer |
| Functional Groups | Aromatic nitro group, phenylalanine backbone |
| Use | Amino acid derivative for peptide synthesis |
| Solubility | Soluble in DMF, DMSO, partially soluble in organic solvents |
| Catalog Number | Varies by supplier |
As an accredited Fmoc-D-2-Nitrophenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled "Fmoc-D-2-Nitrophenylalanine, 1 gram" with hazard symbols, lot number, and manufacturer's details printed clearly. |
| Shipping | Fmoc-D-2-Nitrophenylalanine is shipped in tightly sealed containers, protected from light and moisture. The chemical is typically packed with absorbent materials in compliance with hazardous chemical regulations. Shipping is carried out by certified carriers, often under controlled temperature, with proper labeling and documentation to ensure safe transit and regulatory compliance. |
| Storage | **Fmoc-D-2-Nitrophenylalanine** should be stored in a tightly sealed container, protected from light and moisture. Keep it at 2–8°C (refrigerated conditions). Store in a dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Ensure the workspace is clean and labeled to avoid contamination and degradation of the compound over time. |
Applications of Fmoc-D-2-Nitrophenylalanine in Industrial ManufacturingOur direct manufacturing of Fmoc-D-2-Nitrophenylalanine supports specialized sectors that demand high-purity protected amino acids for advanced peptide synthesis, pharmaceutical research, and biotechnological development. The following application scenarios detail real downstream uses, each with industry-specific compliance, formulation guidelines, and processed product categories. 1. Solid-Phase Peptide Synthesis (SPPS) for Pharmaceutical IntermediatesSPPS remains the core industrial process for producing complex peptide sequences used as active pharmaceutical intermediates. Fmoc-D-2-Nitrophenylalanine introduces D-configuration and unique aromatic functionality that modulates bioactivity in drug candidates. Manufacturers employ it in automated peptide synthesizers, especially during stepwise elongation of sequences involved in peptide hormone analogs and related APIs. Quality control verifies the incorporation efficiency and absence of racemization, responding to strict regulatory requirements. Industry compliance standards
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2. Synthesis of Peptidomimetic Drug CandidatesR&D divisions in pharmaceutical manufacturing select Fmoc-D-2-Nitrophenylalanine to build peptidomimetic scaffolds with increased proteolytic stability and modified receptor affinity. The material provides both steric and electronic modulation vital for candidate optimization studies. Integration occurs in iterative design and synthesis cycles, especially during side-chain or backbone modifications. Analytical documentation and traceability support full data packages for clinical submissions. Industry compliance standards
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3. Manufacture of Research-Grade Peptide StandardsAnalytical laboratories and peptide manufacturers require precision peptide standards for calibration and method development. Incorporation of Fmoc-D-2-Nitrophenylalanine provides critical retention time and mass benchmark in method validation workflows such as LC-MS/MS quantitation. The product supports batch-to-batch consistency and purity profiles demanded under ISO/IEC 17025 and GMP analytical settings, with documentation for traceability and audit readiness. Industry compliance standards
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4. Development of Protease-Resistant Specialty PeptidesBiotech manufacturers engineer peptides for diagnostic and research tools with enhanced stability in biological samples by integrating D-amino acids such as D-2-nitrophenylalanine. This approach increases resistance to proteolytic degradation, essential for in vitro detection reagents and long-term assays. The process demands precise monitoring of stereoisomer incorporation and compatibility with bioconjugation or labeling chemistries without compromising target interaction. Industry compliance standards
Typical usage ratio
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At our chemical manufacturing facility, we focus on specialty amino acids that support precise peptide synthesis and protein engineering. Fmoc-D-2-Nitrophenylalanine has taken a crucial place among these compounds. Over the years, we have seen demands shift from routine L-amino acids to more challenging D-enantiomers. Researchers in biochemistry and medicinal chemistry look for these selective building blocks to push the boundaries of biomolecular design. Our in-house synthesis process for Fmoc-D-2-Nitrophenylalanine responds to these growing needs with reliable quality and traceable consistency. We have refined our process over numerous production runs, prioritizing purity and batch reproducibility because even minor impurities can derail sensitive syntheses.
Fmoc-D-2-Nitrophenylalanine’s relevance goes beyond its core structure. The Fmoc group ensures N-terminal protection during solid-phase peptide synthesis, giving users a streamlined approach to assembling complex peptides with strict sequence control. We use only high-integrity Fmoc derivatives, confirmed by careful NMR and HPLC checks. These added nitro and D-configuration features affect both the chemical reactivity and the biological response of resulting peptides. The nitro group at the ortho-position offers an electronic handle for downstream transformations and site-specific post-synthetic modifications. Among our R&D collaborations, we have seen this molecule serve within enzyme-inhibitor design, probe construction, and the development of novel folding motifs.
Our reputation rests on our ability to supply products that behave consistently batch after batch. Many peptide chemists recall projects upended by unreliable raw materials. Fmoc-D-2-Nitrophenylalanine leaves little room for error. We keep the specification tight, with chemical purity exceeding 98% and enantiomeric excess comfortably above 99%. Moisture content and inorganic residue stay well below typical tolerance ranges, avoiding complications in solid-phase protocols. We manufacture with scale flexibility—gram to multi-hundred-gram lots—so academic and industry partners both receive the same attention to homogeneity, no matter the order size.
Every unit leaves our facility with full documentation, traceable certificates of analysis, and a storage guideline that reflects decades of stability monitoring. Product integrity remains intact across extended transportation and storage windows, supported by controlled packaging atmospheres and tamper-evident seals. Purchasers can trace the source right back to the originating synthesis, a reassurance valued in regulatory submissions and peer-reviewed research.
Some newcomers to the field ask about the practical differences between D- vs. L-2-Nitrophenylalanine or the role of protecting groups. After years of working alongside peptide chemists on troubleshooting and protocol optimization, a few facts stand out. D-configuration amino acids resist enzymatic degradation and alter peptide backbone conformation, which can stabilize bioactive structures or defeat proteases. This simple mirror-image swap opens a broad range of drug design possibilities. We have observed clients use Fmoc-D-2-Nitrophenylalanine to modulate pharmacokinetics or to design sequences that fold or assemble differently compared to their L-analogues.
The Fmoc group stands out among protecting groups for its ease of removal under controlled basic conditions, yielding clear, predictable deprotection and minimal by-product formation. Competitors sometimes release product with partial hydrolysis or contaminated with piperidine-removable debris, causing headaches down the chain. Through repeated direct collaboration, we have honed post-synthetic washing and crystallization steps, giving our product a cleaner baseline.
Our customers’ successes in both research and production feed directly back into our process. Fmoc-D-2-Nitrophenylalanine’s most immediate use remains in solid-phase peptide synthesis. In projects targeting protein-protein interaction inhibitors, this amino acid offers unique steric and electronic traits. Some groups have engineered it into antimicrobial and anti-inflammatory candidates, reporting increased resistance to metabolic breakdown. In fluorescent probe design, the nitro moiety acts as a sensitive reporter for local redox environment. Other clients incorporate it into combinatorial libraries, searching for binding specificity against therapeutic targets where conventional building blocks fall short.
Speaking with groups at both startup biotechs and established pharmaceutical companies, we often hear the same priorities: purity, rapid supply, and reliable, direct technical support. Fmoc-D-2-Nitrophenylalanine from a reputable manufacturer can determine the pace of a medicinal chemistry campaign. Delays or inconsistencies in specialty amino acid supplies have a cascading effect, slowing project milestones and risking costly resyntheses. Avoiding this frustration, we maintain strong relationships with logistics partners and a transparent forecasting approach, so users have clear expectations from inquiry to delivery.
Unlike more routine protected amino acids, D-2-Nitrophenylalanine presents synthetic challenges at scale. As early adopters in the manufacturing community, we optimized key steps—resolution, Fmoc-protection, and side-chain nitroarene handling—to limit racemization and increase yield. Our in-process controls quickly reveal any batch anomalies, so we intervene before impurities accumulate. We have invested in semi-automated purification platforms, reducing manual error and creating smoother scale-up from lab runs to pilot campaigns. Labs running method development or high-throughput screening count on uninterrupted access to critical intermediates like this one.
Producing a specialty amino acid means more than following a published route. We have worked closely with both synthetic organic chemists and downstream application specialists, learning which contaminants threaten troublesome reactions or which solvents best support downstream solid-support deprotection steps. From this multi-decade exchange, our Fmoc-D-2-Nitrophenylalanine supports the next wave of medicinal innovation—from stapled peptides blocking protein-protein interfaces to diagnostic agents reporting on subtle cellular changes.
The growth of peptide therapeutics and peptidomimetics raises the bar for material quality. Regulatory standards expect full traceability, batch documentation, and impurity profiles. For projects advancing into preclinical or IND-enabling studies, any irregularity in stereochemical purity or contaminant load can invalidate an entire program. Over the past decade, we have provided GMP-supporting documentation and robust impurity maps to institutions preparing submission dossiers.
We have watched the literature evolve as D-amino acid-containing peptides make their way from patent filings through to first-in-human studies. High-fidelity chiral production stands at the foundation of this progress. Our technical staff provides direct support to synthesize researchers seeking custom lot sizes or assistance with protocol troubleshooting. When our facility adopted new in-line analytics, we brought in working scientists who had faced failed couplings due to unreliable starting material.
Advances in unnatural amino acid chemistry feed innovation far beyond academic research. In our network, customers working in materials science use Fmoc-D-2-Nitrophenylalanine to design metal-coordination scaffolds and stimuli-responsive hydrogels. The ortho-nitro group creates hydrogen-bonding and electron-donating environments not found in natural proteinogenic residues, opening the door to precisely tuned folding and self-assembly properties.
Some of our most engaging projects have involved linking D-2-Nitrophenylalanine into optoelectronic films where chirality and electronic function come together. The same batch that supports a high-throughput medicinal library might also appear in a bio-inspired material that changes color in response to environmental cues. Working as manufacturers rather than intermediaries, we share in the intellectual stakes—our commitment to material science stretches beyond a sales transaction into process knowledge and long-term problem-solving.
A reliable synthesis pathway means more than a reproducible chemical process. Each customer presents subtle challenges—changes to solvent protocols, choice of coupling reagent, or modifications to cleavage conditions. Our staff has fielded late-night calls from scientists perplexed by incomplete deprotection or by unexpected side reactions on the 2-nitro ring. Experience building this compound in-house gives us a unique perspective on troubleshooting, from root-cause analysis to concrete, tried-and-tested solutions.
We organize regular training and Q&A sessions for both novice and expert users, bringing together feedback from across industry sectors. From university groups probing protein conformational change to contract manufacturers scaling up clinical candidates, we treat every technical support request as a learning opportunity. This hands-on approach lets us identify trends—rising demand for D-enantiomers, requests for higher bulk packaging stability, or growing interest in green synthesis modifications.
Innovation never remains static in chemical manufacturing. We consistently revisit our synthesis of Fmoc-D-2-Nitrophenylalanine, probing new protecting group strategies or alternative chiral catalysts. Current process development aims to streamline purification, cut down on solvent waste, and explore greener work-up solutions. We confer with academic advisors and industrial partners to adjust our process to emerging best practices.
This work has yielded shorter production timelines and higher yields across scales. A large part of this progress comes from direct feedback. A project manager at a partner institution once detailed how a barely-detectable trace impurity led to spectral overlap on a gradient elution, compromising downstream analytics. We refined our purification based on these insights, sharpening our impurity cutoffs even below internal baseline requirements.
Research timelines can hinge on rapid, hassle-free procurement. Over the years, purchasing departments and lab supervisors have shared how convoluted quoting, inconsistent lead times, or uncertainty over provenance disrupt project flow. Direct engagement with our facility means access to fresh, high-integrity lots, ready for same-day dispatch where possible. We keep our online systems responsive, cutting down on idle time between inquiry and shipment.
We handle all administrative steps—from documentation to SDS provision—internally. Research groups frequently require expedited documentation for funding, publication, or regulatory review, and our technical support team bridges this gap. In project meetings, our staff presents material use-cases backed by analytical data, supporting clear communication between procurement and bench researchers.
The use of specialty, functionalized D-amino acids will only increase as therapeutic designs become more sophisticated. Every batch of Fmoc-D-2-Nitrophenylalanine produced in our plant reflects a close-knit process—from strategic sourcing and analytical screening through hands-on packaging and technical consultation. We have watched research transform as new chemical tools bring more control to molecular assembly.
Our ongoing investments in both manufacturing equipment and direct customer engagement anchor us firmly in E-E-A-T (Experience, Expertise, Authority, Trustworthiness) values. Production improvements are driven by firsthand feedback and practical problem-solving more than by theoretical efficiency gains. This focus on usability, transparent operation, and strong scientific partnership means the research community can depend on prompt, accurate delivery—backed up by authentic, comprehensive support. Every successful experiment, publication, and product built with this key building block strengthens our shared mission.