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HS Code |
739428 |
| Chemical Name | D-3-Nitrophenylalanine |
| Molecular Formula | C9H10N2O4 |
| Molecular Weight | 210.19 g/mol |
| Cas Number | 2120-22-3 |
| Appearance | White to light yellow solid |
| Chirality | D-isomer |
| Melting Point | Approx. 195-197°C |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Iupac Name | (2R)-2-amino-3-(3-nitrophenyl)propanoic acid |
| Storage Conditions | Store in a cool, dry place at 2-8°C |
| Synonyms | D-3-(Nitrophenyl)alanine |
As an accredited D-3-Nitrophenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 1 gram of D-3-Nitrophenylalanine, sealed with a screw cap, and labeled with product details and safety information. |
| Shipping | D-3-Nitrophenylalanine is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be transported under controlled room temperature, away from direct sunlight and incompatible substances. Compliance with relevant chemical shipping regulations and safety guidelines is necessary, with proper labeling and documentation to ensure safe handling and delivery. |
| Storage | D-3-Nitrophenylalanine should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, well-ventilated area. Ideally, the storage temperature should be at 2–8°C (refrigerator). Avoid exposure to incompatible substances, such as strong oxidizers. Ensure proper labeling and keep away from food and drink sources. Follow local safety regulations for chemical storage. |
Applications of D-3-Nitrophenylalanine in Industrial ManufacturingAs an established producer of D-3-Nitrophenylalanine, we supply this high-purity amino acid derivative for precise applications in advanced chemical synthesis, pharmaceutical intermediates, peptide production, and biochemical research. Each scenario below details its specialized use within the manufacturing value chain, focusing on key operational parameters essential for downstream users. 1. Chiral Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use D-3-Nitrophenylalanine as a chiral building block during the synthesis of active pharmaceutical ingredients (APIs) such as peptide-based therapeutics and beta-lactam antibiotics. The material’s high stereochemical purity enhances enantioselective reactions, particularly in multi-step syntheses where controlling the stereochemistry is critical for achieving regulatory approval. It typically enters the process during the early or intermediate reaction stages, where it couples with other protected amino acids or intermediate scaffolds. Production batches must meet strict traceability and impurity profiles, and documented compliance is required at each stage. Industry compliance standards
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2. Peptide Synthesis for Research and Diagnostic KitsResearch laboratories and diagnostic reagent manufacturers utilize D-3-Nitrophenylalanine in custom peptide assembly processes, often as a site-specific amino acid analog to adjust structural properties or signal moieties in test kits. The compound is favored for its ability to introduce UV-active or electron-withdrawing groups, supporting both structural study and detection capabilities. Integration takes place during solid phase peptide synthesis (SPPS) with automated synthesizers, where high coupling efficiency and low racemization are priorities. Industry compliance standards
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3. Synthesis of Chiral Catalysts and LigandsChemical and material companies apply D-3-Nitrophenylalanine when synthesizing chiral catalysts or ligands for asymmetric catalysis, integral to producing high-value enantiomerically pure specialty chemicals. The unique nitroaromatic side chain supports coordination to transition metals and improves selectivity in asymmetric hydrogenation or coupling reactions. The material enters catalyst precursor synthesis during multi-step organometallic assembly, where rigorous impurity controls and metal ion compatibility checks are performed to comply with industrial catalyst QC standards. Industry compliance standards
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4. Amino Acid Derivative Reference Standards for Analytical LabsAccredited QC and analytical laboratories incorporate D-3-Nitrophenylalanine as a reference standard to establish calibration curves and validate analytical methods, specifically for chiral HPLC and mass spectrometry protocols. The compound’s high purity and resolved optical activity are essential for reliably quantifying trace impurities or peptide fragments in batch release testing. The material is introduced in analytical sample preparation steps, typically after dissolution in controlled solvents, for benchmarking method sensitivity and repeatability. Industry compliance standards
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In the laboratory and pilot plant, D-3-Nitrophenylalanine stands out for chemists seeking high-precision building blocks. Over the years, we've refined each step of the process—developing this compound as one of the most dependable aromatic amino acid derivatives available. The model produced in our facilities upholds strict chiral integrity and presents a consistently high purity, which remains crucial for research and advanced synthetic applications.
Researchers and production managers continually reach out to us, asking about advantages or challenges in working with D-3-Nitrophenylalanine as compared to its L-enantiomer or similar nitrophenyl derivatives. From experience, the distinct features start at the atomic arrangement: the D-configuration influences not just stereospecific interactions in enzyme studies and peptide engineering, but also affects the outcome in structure-activity relationship work. Many find this product solves particular hurdles in structure-function mapping in peptide and pharmaceutical research.
Our customers put high value on reliable specifications. Each batch undergoes rigorous testing—HPLC, NMR, mass spectrometry, and chiral purity analysis. Years of technical adjustments ensure tight control over moisture content, particle size, and residual solvent levels because quality assurance directly supports downstream performance. We maintain a standard that removes ambiguity; our analytical documentation delivers clear chromatograms and spectra alongside every shipment. Uncertainties haven’t had room to take root, since our own research and daily QC protocols push us to keep tightening these documentation standards.
Notably, D-3-Nitrophenylalanine’s crystalline solid form preserves stability during transport and long-term storage. Working chemists often ask about lot-to-lot reproducibility—a valid concern given the subtle differences a single misaligned chiral center could introduce in synthesis or screening. By handling entire production chains—starting from protected intermediates through to recrystallization and drying—we make sure output remains consistent, sparing researchers from wasting time troubleshooting unnecessary variability.
The most common demand for this product comes from peptide synthesis labs, biocatalysis researchers, and pharmaceutical R&D groups. D-3-Nitrophenylalanine’s D-configuration resists proteolysis, which opens doors for those engineering peptide chains with enhanced metabolic stability. Such modifications give teams the ability to push beyond the common amino acid palette, unlocking new bioactive molecules that would degrade too quickly if built only with L-forms.
Custom enzyme design projects often turn to this compound. Its aromatic nitro group doesn’t just provide a handle for later derivatization—it also impacts the electronic environment in enzyme binding sites. Scientists focused on enzyme mechanism or seeking to tailor substrate specificity value this kind of selectivity. D-3-Nitrophenylalanine can act as both a substrate analog and as a probe. By inserting it where traditional amino acids would fail, researchers delineate key structure-activity relationships more precisely.
We’ve followed drug discovery teams as they work with model peptides and peptidomimetics that rely on stubborn resistance to metabolic breakdown. Sponsors frequently demand stability data at every stage of development, which puts pressure on us to deliver the cleanest, most unambiguous product possible. Each additional purification and documentation step we run in our production line reflects the needs voiced by trial sponsors and regulatory reviewers.
Direct communication with end-users has led us to adapt more than once. Not long ago, a university peptide chemist described issues coordinating their cleavage cocktail with nitroaromatic residues. After several iterations, we learned that extended drying periods post-synthesis improved compatibility with their resin cleavage procedures. The solution emerged only after reviewing actual field conditions—not just relying on theoretical data. These stories surface in our regular feedback sessions, shaping how production tweaks evolve over the years.
Formulation and process development chemists tend to struggle with solubility issues or reprocessing batches when dealing with lesser-purified derivatives. We’ve developed a manufacturing protocol—mindful of solvent selection and crystallization kinetics—that reduces these headaches. In practical terms, a well-resolved sample of D-3-Nitrophenylalanine can make the difference between a stalled reaction and a successful multi-step synth. The goal, each round, stays the same: eliminate unknowns that turn up in chromatograms or during evaporation steps, which speed up the workflow for those on tight schedules.
Years spent troubleshooting across many scales—gram quantities for academic labs or multi-kilogram for industry—have given us a candid view of the real issues. It’s rarely the published procedures alone that dictate successful synthesis. Reproducibility, ease of handling, and the right documentation come up again and again in calls and messages from customers. These are the themes we address directly, upgrading filtration procedures, simplifying packaging, and offering real-time analytical support as needed.
Many visitors ask for a breakdown of how D-3-Nitrophenylalanine compares with L-3-Nitrophenylalanine or even the unmodified base amino acid. The D-form specifically blocks most enzymes from recognizing and cleaving peptide bonds, which brings a clear advantage for in vivo applications where metabolic half-life matters. Early-stage development teams, especially those engaged in exploring next-generation peptide drugs, find that this single stereochemical tweak could mean weeks saved in degradation studies.
Some labs attempt in situ racemization, swapping L- for D-forms via chemical manipulation. From production experience, direct synthesis yields cleaner, more defined material than any such conversion. Each step that avoids potential epimerization or byproduct formation keeps analytical signatures cleaner and end results more predictable. By investing in D-specific protection and coupling chemistries, we sidestep the tangle of impurities that dog less discriminating synthetic approaches.
Though other nitrophenylalanine analogs exist—substituted at different positions on the ring—the ortho (3-) positioning in this product impacts the steric and electronic character distinctly. In enzyme engineering and bind-and-release studies, this subtle reactivity can make or break an experiment. Our longtime collaborators in structural biology appreciate the difference even slight ring substitutions have on crystal packing and resolution, so maintaining positional specificity pays dividends on every scale.
Scaling production of high-purity chiral amino acid derivatives presents several recurring technical hurdles. Even a minor slip in protecting-group strategy or temperature control during hydrogenation can spiral into costly reprocessing. As demand for D-3-Nitrophenylalanine picked up globally—especially for pharmaceutical validation lots—we invested in closed-system reactors and automated crystallization monitoring. Every revision to our pipeline comes out of identifying where human factors or legacy equipment could introduce noise into a process.
Waste minimization matters at both financial and environmental levels. By tightening up yields and enhancing solvent recovery, we cut down not just on direct production costs, but also on the time and documentation required for compliant waste disposal. Reducing our footprint through solvent recovery and energy-efficient drying steps has become a point of pride. Enhanced traceability—made possible with tighter digital batch records and barcoded lots—provides both our team and our clients the security that every drum and bottle matches exacting standards.
We’ve faced steep learning curves bringing our workers up to speed on the finer points of chiral separation and optical rotation determination. Regular training and certification, plus internal QC competitions, have directly translated into lower batch rejection rates. These incremental gains, often invisible on paper but critical in day-to-day operations, set apart our approach from hastily brokered supply deals or third-party resellers with thin quality oversight.
Supplying a chiral compound to the research sector keeps us rooted in the wider scientific conversation. We regularly field requests for custom documentation—sometimes it’s more detailed impurity profiles, sometimes it’s new stability protocols or resistance to specific stress testing. Our technical team participates in early-stage project meetings with select clients, offering insight that can help avoid late-stage surprises. By attending scientific conferences and hosting roundtable sessions, we stay tuned in to both emerging needs and trends shaping R&D worldwide.
With regulatory expectations evolving as new molecules progress toward clinical or industrial applications, validation practices have moved up a notch. We have set up risk management and documentation protocols that preempt most common red flags in audit scenarios. Maintaining transparency around batch-to-batch consistency and providing certified reference samples allows teams on the receiving end to accelerate their validation steps.
No less important is intellectual property. We recognize the need for a clean supply chain, where every intermediate and precursor is sourced and documented to avoid weak links. Those in the contract manufacturing space, as well as pharma and biotech clients, lean heavily on our internal chain-of-custody controls.
As the scientific community moves ahead with more ambitious peptide libraries, targeted enzyme studies, and theranostic probes, D-3-Nitrophenylalanine’s role continues to expand. Areas such as site-specific protein labeling, mechanistic enzymology, and non-natural peptide design invite further iteration with increasingly complex modifications. Our R&D group dedicates a portion of each production run to trialing next-generation protection schemes and developing new purification strategies. These efforts are informed by emerging concerns around micro-contaminants, storage stability for shipping in varied climates, and the push toward more sustainable chemical processes.
Challenging project briefs sometimes require custom scale-up campaigns with tailored documentation libraries and advanced impurity profiling. In these projects, our team sits alongside partner researchers, not merely as a vendor, but as an active technical voice—exploring what each modification or parameter tweak could mean for project success. Maintaining an open channel for real-time problem solving has inevitably forged deeper trust on all sides.
We’re seeing growth not just in pharmaceutical applications but in fields as diverse as agricultural science, probe development for imaging, and biomaterials. Peptides incorporating D-3-Nitrophenylalanine have already entered large-scale screening for environmental sensors and bioactive films.
A core part of our work lies in active listening. Constructive criticism and field reports—positive and otherwise—have pushed the evolution of this compound’s production quality over time. In response to one recurring concern around dissolution in certain solvents, our team adjusted milling parameters and performed collapse testing to optimize powder handling. These changes weren’t born of market dictates; they benefited from the back-and-forth with graduate students, research fellows, and production coordinators.
We also share insights on process optimization and troubleshooting, helping labs avoid common missteps with chiral reagents. Direct dialogue has a measurable effect on reducing waste, boosting yield, and preventing rework. Hosting technical workshops and online Q&A sessions as part of our commitment to responsible manufacturing adds depth to these partnerships. It’s good science, but it also makes good business sense to grow alongside those pushing the field forward.
Colleagues occasionally ask about regulatory abbreviations or storage specs, and we maintain a library of supplementary documents and FAQs, though our main mission stays focused on clear real-world performance. Being responsive, updating procedures when gaps or oversights surface, lets us build confidence among both newer entrants and seasoned project managers.
After years closely involved with D-3-Nitrophenylalanine—through pilot batches, scale-up headaches, research collaborations, and late-night troubleshooting—it becomes clear that the success of this compound for modern labs depends on more than safe packaging or generic documentation. Real-world feedback, rigorous testing, and a willingness to innovate at every step have pushed the boundaries of what researchers can achieve with non-standard amino acid derivatives.
We see our work as pushing alongside the entire innovation sector, linking deep technical knowledge to practical supply chain logistics. Each gram of D-3-Nitrophenylalanine leaving our facility carries years of iteration, adaptation, and shared experience. It’s the line-by-line review of QC data, the quick response to a researcher’s troubleshooting call, and the shared goal of pushing discovery a bit further that keeps the product relevant and reliable.
As demands shift and research frontiers move, we continue to treat each request or suggestion as a prompt to do better. Our commitment: keep refining the product, remain available as a technical partner, and help carry new ideas from the benchtop to the marketplace with confidence.