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4-Nitro-L-Phenylalanine Monohydrate

    • Product Name 4-Nitro-L-Phenylalanine Monohydrate
    • Alias 4-NO2-L-Phe
    • Einecs 249-477-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    915137

    Chemical Name 4-Nitro-L-Phenylalanine Monohydrate
    Synonyms p-Nitro-L-phenylalanine monohydrate
    Molecular Formula C9H10N2O5
    Molecular Weight 226.18 g/mol
    Cas Number 7149-10-2
    Appearance Light yellow to yellow solid
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Solubility Soluble in water
    Melting Point 225-227°C (dec.)
    Optical Rotation [α]20/D +27° to +31° (c=1, H2O)

    As an accredited 4-Nitro-L-Phenylalanine Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 4-Nitro-L-Phenylalanine Monohydrate, sealed with screw cap and labeled for laboratory use.
    Shipping 4-Nitro-L-Phenylalanine Monohydrate is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous chemical, requiring appropriate labeling and safety documentation. Shipping complies with international and local regulations, often via ground or air transport, with temperature and handling conditions maintained according to safety guidelines.
    Storage 4-Nitro-L-Phenylalanine Monohydrate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2-8°C (refrigerator). Ensure proper ventilation in the storage area and avoid exposing the chemical to incompatible substances such as strong oxidizers. Clearly label the container and restrict access to authorized personnel only.
    Application of 4-Nitro-L-Phenylalanine Monohydrate

    Applications of 4-Nitro-L-Phenylalanine Monohydrate in Industrial Manufacturing

    Our production of high-purity 4-Nitro-L-Phenylalanine Monohydrate supports advanced manufacturing sectors by supplying consistent quality and regulatory-compliant material for tightly specified industrial and research applications. As a manufacturer with direct process experience, we collaborate closely with leading partners in specialty chemicals, life sciences, and pharmaceutical synthesis to meet stringent global standards from laboratory scale up to industrial volumes.

    1. Peptide Synthesis for Pharmaceutical Research

    In pharmaceutical peptide and peptide-mimetic drug research, 4-Nitro-L-Phenylalanine Monohydrate serves as a highly specific protected amino acid analogue that incorporates a nitro group into synthetic sequences for subsequent chemical transformation, binding studies, and structure-activity relationship investigations. Our material finds critical use in solid-phase peptide synthesis (SPPS) and solution-phase protocols requiring precise incorporation with minimal by-product formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • Pharmacopoeia standards: USP, EP, JP (for research/intermediate grade raw materials)
    • ISO 9001 certified quality management systems
    • REACH registration (Europe) for substance import/export traceability

    Typical usage ratio

    • 0.5–2.5 mol% per total amino acid residues in the peptide chain, based on site-specific residue sequence and peptide length. Adjusted according to the desired incorporation point and target final concentration.

    Downstream process integration

    • Direct charge to automated SPPS resin reactors during initial chain assembly or as a targeted replacement for standard phenylalanine units in parallel synthesis.
    • Deprotection steps require controlled acid/base treatment to preserve the nitro functionality while completing peptide coupling cycles.

    Final product types

    • Pharmaceutical research peptides containing site-specific nitro-aromatic residues
    • Bioactive peptide libraries for early-stage drug screening
    • Modified peptide substrates for enzyme or receptor binding assays
    • Pharmacological intermediates used in structure-activity studies

    2. Activity Probes and Bioorthogonal Labeling

    Biotechnology and proteomic research groups utilize 4-Nitro-L-Phenylalanine as a chemical handle for post-synthetic reduction and coupling reactions. The nitro group enables selective transformations to amine or azo derivatives, supporting development of fluorescence and affinity-based activity probes within complex biological samples.

    Industry compliance standards

    • ISO 13485 for research reagent traceability (where applicable)
    • OECD Good Laboratory Practice (GLP) guidelines for reagent manufacture and QC
    • Relevant chemical safety and transport compliance: UN Model Regulations, IATA, ADR

    Typical usage ratio

    • 0.1–1.0% w/w in protein modification reagent formulations, adjusted according to molecular target load and labeling protocol.

    Downstream process integration

    • Covalent incorporation into peptide chains or proteins during synthetic or enzymatic labeling steps prior to probe derivatization.
    • Selective nitro group reduction as a trigger for further bioorthogonal chemistry or conjugation to fluorescent dyes and tags.

    Final product types

    • Chemical biology labeling probes for cell imaging and target identification
    • Affinity-tagged enzyme substrates and inhibitors
    • Advanced diagnostic reagents for biochemical assays

    3. Reference Standards for Analytical Method Validation

    Analytical laboratories and QC units across the pharmaceutical, chemical, and environmental sectors demand precise reference materials for HPLC, LC-MS, and other chromatographic system calibrations. 4-Nitro-L-Phenylalanine Monohydrate provides a high-purity analyte for the establishment of retention time standards and for the evaluation of nitro-aromatic amino acid impurity profiles in API synthesis and environmental testing.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory competence testing
    • USP General Chapters <621> and <1225> for chromatographic system suitability
    • FDA cGMP guidelines for reference materials in drug manufacturing
    • JCGM 100:2008 – “Evaluation of measurement data – Guide to the Expression of Uncertainty in Measurement” (GUM)

    Typical usage ratio

    • 100–500 ppm as standard analyte concentration in mobile phase or sample spiking protocols; final level depends on instrument calibration requirements and detection limits.

    Downstream process integration

    • Preparation of calibration curves, system suitability, and performance qualification procedures in QC lab workflows
    • Reference solution blending prior to validation or release testing of active ingredients and finished goods

    Final product types

    • Certified reference standards for analytical laboratories
    • Chromatographic system suitability kits
    • Method validation packages for regulated manufacturing environments

    4. Chemical Intermediates in Agrochemical Active Ingredient Synthesis

    In specialty agrochemical manufacturing, 4-Nitro-L-Phenylalanine Monohydrate serves as a niche intermediate for the preparation of aromatic amino acid derivatives that contribute to the synthesis of plant growth regulators, enzyme inhibitors, or experimental crop protection compounds. Its defined nitro functionality allows for controlled downstream reduction and coupling steps essential for precision molecular design.

    Industry compliance standards

    • FAO/WHO specifications for pesticide and plant protection product intermediates
    • ISO 9001-based supply chain traceability
    • EU Regulation (EC) No 1107/2009 on plant protection products for substances used in active ingredient synthesis

    Typical usage ratio

    • 1–10% by weight of target batch size, adjusted for required equivalence in stepwise synthesis routes and conversion efficiency during scale-up.

    Downstream process integration

    • Reactive charge in aromatic substitution or amination coupling reactions following reduction of the nitro group
    • Intermediate purification stages prior to final active ingredient addition and formulation

    Final product types

    • Intermediates in selective herbicide R&D pipelines
    • Building blocks for plant metabolic pathway modulators
    • Research-grade crop protection development compounds

    5. Advanced Organic Synthesis for Specialty Chemical Manufacturing

    Chemical processors and contract manufacturers rely on 4-Nitro-L-Phenylalanine derivatives as scaffolds in advanced heterocycle and dye synthesis. The aromatic nitro function enables regioselective reductions and coupling, playing a central role in multi-stage synthesis pathways for specialty colorants and analytical dyes used in research, electronics, or imaging applications.

    Industry compliance standards

    • ISO 9001 for specialty chemical production workflows
    • Responsible Care Global Charter for chemical safety
    • REACH registration for European custom synthesis

    Typical usage ratio

    • 0.5–5 mol% of total reaction input, adapted to the specific substitution pattern required and the overall synthetic plan.

    Downstream process integration

    • Starting material for nitro-aromatic reduction followed by amide or aniline condensation steps
    • Integration into custom multi-step syntheses requiring chiral amino acid inputs

    Final product types

    • Intermediates for fine chemical manufacturing
    • Heterocycle precursors for organic dye synthesis
    • Specialty analytical stains and reagents
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    Certification & Compliance
    More Introduction

    Introducing 4-Nitro-L-Phenylalanine Monohydrate: A Direct Perspective from the Manufacturer

    Every day in our production facility, we see the careful precision that goes into manufacturing specialty amino acids. 4-Nitro-L-Phenylalanine Monohydrate stands out among them. This product allows research chemists and peptide scientists to access a rare structural motif with genuine reproducibility—something we can only achieve after years refining our process. The appearance of this compound, the pale-yellow powder, is no accident. Each batch is the result of precise controls at every step, meticulous purification, and consistent raw material quality.

    Product Overview

    4-Nitro-L-Phenylalanine Monohydrate, CAS number 5467-70-9, holds a stable place in our catalog. Its molecular formula C9H10N2O5•H2O gives a hydrate that behaves reliably both on the bench and in scaled production. With a purity of ≥ 98% (HPLC traceable), and water content consistently measured batch-to-batch, this version meets the elevated needs of research in chemical biology and pharmaceutical development. Every lot we prepare is checked by NMR and MS; our on-site technical team logs spectral data for every shipment. This level of care supports regulatory documentation and answers every question customers may have about what goes into their labs.

    Understanding the Applications in Practice

    Researchers working at the interface of chemistry and life sciences push the envelope of what engineered amino acids can do. Every scientist needing site-specific protein labeling, probe design, or orthogonal translation requires niche amino acids such as 4-Nitro-L-Phenylalanine Monohydrate with solid provenance—not just a certificate on the box. We’ve seen demand rise as more protein labeling platforms emerge. Scientists incorporate this product into ribosomal translation systems for studying protein folding and trafficking. Some use it to construct peptide-based frameworks that explore nitroaromatic chemistry, allowing unique ways to introduce spectroscopically active or reactive handles.

    Regular L-phenylalanine just cannot provide these functions. Once the nitro group enters the para position, electron distribution and sterics transform the molecule. 4-Nitro-L-Phenylalanine resists direct substitution reactivity and delivers the electron-withdrawing effect needed in specialized peptide syntheses. Protein engineers exploit this difference for bioconjugation or photocleavable linker development. Sometimes our customers contact us to discuss exactly how their buffer systems interact with the monohydrate form—the extra water plays a role in solubility, storage, and even crystallization outcomes.

    Clarifying the Value Behind Genuine Manufacturing

    The world of specialty amino acids is full of shortcuts. Traders, brokers, and secondary suppliers sometimes re-label material—potentially compromising reproducibility. As the primary manufacturer, we personally manage every step. The nitrosation and subsequent purification process bring about subtle challenges: control of oxidation, removal of impurities, and protection of the L-configuration throughout. Years ago, supply of high-purity 4-Nitro-L-Phenylalanine suffered from batch variation and trace byproduct contamination. Few could anchor their product guarantees in observed outcomes. We developed a system where quality control relies on no fewer than three analytical platforms and people who can spot oddities that machines miss.

    From solvent choice during synthesis to filtration techniques and cold-room storage protocols, every parameter matters. It comes down to people, not just specs. Lab-scale production batches may seem simple, but challenges explode during scale-up. Precipitation can shift, water content drifts, and the risk of racemization always lurks. We have learned to trust regular Karl Fischer titration readings for the monohydrate to keep performance consistent. Any manufacturer who fails to monitor these routinely risks backing their customers into a corner. We have addressed such pitfalls by investing in employee training, facility upgrades, and robust documentation. This allows us to deliver 4-Nitro-L-Phenylalanine Monohydrate that performs the same whether a customer orders a few grams or several kilograms.

    Key Differences From Other Phenylalanine Derivatives

    Fellow chemists sometimes ask what sets this compound apart from other derivatives. Some might assume all para-substituted phenylalanine analogs behave similarly, but real-world experience tells a different story. For example, 4-Fluoro- and 4-Chloro-L-Phenylalanine, with their respective halogen substituents, exhibit entirely distinct electronic effects and downstream reactivities. Nucleophilicity and susceptibility to oxidative stress change with the nature of the para group. The nitro group’s strong electron-withdrawing character alters the acidity at the amino and carboxyl ends. Through hands-on formulation, we’ve found this influences peptide chain incorporation. Analogs with lesser substituents might go right through peptide synthesis, while the nitro variant will sometimes need extra monitoring during Fmoc solid-phase protocols.

    Another misconception involves monohydrate versus anhydrous forms. Removing water may sound like an upgrade but it can encourage aggregation and reduce shelf-life under practical conditions. For us, the monohydrate offers a sweet spot: easier handling and consistent weighing, crucial in multi-step syntheses and analytical reconfirmation. Each form fits a purpose, but our in-facility trials show that the monohydrate is adaptable and less likely to cake or degrade during standard ambient storage.

    Tracing the Manufacturing Experience

    Years spent scaling 4-Nitro-L-Phenylalanine Monohydrate from laboratory vials to industrial quantities taught us the limits of textbook chemistry. Control over nitrosation, pH drift, temperature spikes, and mother liquor disposal all steer product quality. Early on, we lost yield to dissolved oxygen fluctuations and inconsistent stirring rates. Now, every fermenter and reaction tank has been fitted with redundant controls and logged oversight. The same finished powder shows up on analyst benches in North America, Europe, and East Asia, passing the same HPLC and NMR checks no matter where it lands.

    Production teams swap notes not just about technical specs, but lived experiences. A high yield in a single batch means little if the next fails compliance. Consistency is king. Direct oversight lets us troubleshoot and turn around customer queries fast. One research partner flagged an issue with trace ion contamination—our access to every processing step let us spot the root problem in solvent prep and adjust our protocol that very week. Story after story comes out of this kind of hands-on approach. In every shipment leaving our dock, we include spectral data, batch records, and clear transparency about raw material sources. Our approach is based on the idea that every gram matters—not just as inventory, but as a reflection of years spent mastering the chemistry.

    Supporting the Scientific Community With Real Data

    Academic groups studying enzyme active sites or pharmaceutical labs engineering new peptidomimetics want evidence and accountability. We rarely hear demands for generic paperwork; instead, collaborators want IR scans, chromatograms, or even hands-on advice about solid-phase coupling. Our technical support, drawn from real-world manufacturing floors and troubleshooting sessions, has helped countless teams optimize protocols. 4-Nitro-L-Phenylalanine Monohydrate sometimes reveals unexpected side-reactions during peptide chain extension. Teams without direct manufacturing knowledge might misattribute yield issues to their own set-up. We know from internal R&D how reagents interact with trace moisture, how pH drift can accelerate hydrolysis, and what pre-coupling drying is most effective. Scientists come to us asking about salt forms, counter-ions, and impurity risks because they know we see the inside of every process.

    The compound rarely causes unnecessary hurdles when stored correctly in a desiccator, away from light and excessive heat. Its shelf stability has been borne out by three-year retain sample programs. We check not just for institutional compliance but to spot potential trends before they affect users. During one run, trace iron contamination resulted from an old batch of reaction vessels. Because our internal controls flagged an analytical anomaly, we pulled the lot before it ever went out. This focus on traceability and accountability reflects our manufacturing DNA. For every purchase, we provide technical resources, practical recommendations from our chemists, and open dialogue about challenges researchers may face.

    Why Sourcing Direct From the Manufacturer Matters

    In a market with so many intermediaries, the origin story of a compound can be obscured. Buying direct from the manufacturer translates into full visibility—not just of composition, but also of process changes and lifetime data. Many research groups report differences in performance that can be traced right back to batch-to-batch variation from resellers lacking process oversight. We document every part of the chain: from sourcing certified raw phenylalanine, through nitrosation, all the way to the packaging room. Tight process controls and in-house technical knowhow mean that if a challenge arises, the person answering the phone or email has access to everyone involved in making the lot. That level of access helps projects move forward without days lost to bureaucratic back-and-forth.

    Direct communication also demystifies any issues involving regional regulatory compliance. Each territory may have its own evolving requirements for research use chemicals. We work across North America, the EU, and Asia to provide regulatory support—offering complete certificates of analysis, full MSDS documentation, and up-to-date import/export advice. Labs often face rapidly changing guidelines. Having firsthand manufacturing knowledge, and the ability to adapt quickly to new standards, means we help customers anticipate snags instead of struggling with them at the last minute.

    The Impact of Monohydrate on Research Outcomes

    Handling differences between the monohydrate and anhydrous forms goes beyond just water content. Researchers running syntheses and chromatography consistently tell us the monohydrate dissolves more gently and resists static clumping, reducing waste and making precise measurements easier. We have always believed this puts research teams in control. Peptide chemists who tried both versions often come back to the monohydrate—citing cleaner baselines in HPLC traces and more manageable sample prep. The monohydrate’s granular consistency prevents dusting, reduces exposure, and improves accuracy when scaling reactions from milligram to gram quantities.

    One university group pursuing photoactive peptide probes gave us direct feedback: the monohydrate’s improved stability in their humid lab kept their samples active over several weeks, whereas the anhydrous form had suffered minor hydrolysis at the same time. Their project timeline stayed on track, as there was no need to repeat syntheses or troubleshoot unexplained performance dips. These outcomes, echoed in multiple labs, prove that the technical nuances of manufacturing directly influence published research.

    Common Questions and Field Observations

    Fielding questions from teams working in organic synthesis or protein chemistry reflects the practical side of our experience. Many ask whether the introduction of a nitro group at the para position affects downstream modifications like N-alkylation or reductive amination. Our internal R&D teams can structure these reactions and advise on ideal buffers, coupling reagents, and temperatures based on hundreds of trial runs. Our feedback loop—starting at the reaction tank and ending in research labs—lets us provide meaningful updates, so customers know what to expect.

    We also see trends across disciplines. Demand rises with advances in cell imaging and marker technology, where nitroaromatic moieties function as reporters or photo-switch elements. Our feedback from medical device companies has flagged application-specific requirements, such as minimizing residual solvents or confirming bioburden post-packaging. In every case, our technical team works with product managers and QC analysts to tune process steps, rely on GMP-grade raw materials when needed, and maintain rigorous cleaning validation standards.

    Our certainty in offering 4-Nitro-L-Phenylalanine Monohydrate with this level of reliability does not come from sitting in an office. It comes from hands-on problem-solving on the production floor, troubleshooting with industry collaborators, and keeping records open for everyone in the chain. Labs that choose our material gain not only chemical consistency but access to decades of manufacturing insight.

    Looking Toward Future Developments

    As peptide therapeutics, probe development, and advanced protein engineering mature, the need for niche, high-purity building blocks will continue to grow. Researchers will look for compounds that provide unique functionality and predictability. 4-Nitro-L-Phenylalanine Monohydrate is already shaping the toolkit available to innovators. Our ongoing investment in analytical instrumentation, automation, and staff expertise keeps us at the leading edge—not by chasing buzzwords, but by paying attention to what works on the bench and in production.

    Collaboration and feedback cycles remain central to our approach. We routinely adjust protocols based on real-world usage data, whether that means tightening tolerances, innovating packaging formats to reduce waste, or adjusting purification to address the next generation of experimental design. Our customers gain a product shaped by lived manufacturing challenges, not just theoretical design. It is a difference our partners recognize once they work with material whose quality holds fast throughout the entire project timeline.

    Conclusion: In Practice, Quality Counts

    Anyone can list specifications and purity figures. The true test of a chemical manufacturer’s commitment comes from lived responsibility. We stand behind 4-Nitro-L-Phenylalanine Monohydrate not just as an entry in a catalog but as the result of sustained investment, experienced people, and technical diligence. Our process makes all the difference: complete ownership from raw material to finished lot, deep product knowledge, and open communication with every customer. The result: a specialty amino acid that works as reliably for the first sample as for the thousandth, empowering researchers worldwide to advance their science with confidence.