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4-Nitrocinnamaldehyde

    • Product Name 4-Nitrocinnamaldehyde
    • Alias p-Nitrocinnamaldehyde
    • Einecs 220-968-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    307865

    Chemical Name 4-Nitrocinnamaldehyde
    Cas Number 619-75-0
    Molecular Formula C9H7NO3
    Molecular Weight 177.16
    Appearance Yellow crystalline solid
    Melting Point 207-211°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.36 g/cm³
    Smiles C1=CC=C(C=C1)C=CC=O[N+](=O)[O-]
    Inchi InChI=1S/C9H7NO3/c11-6-5-8-1-3-9(4-2-8)10(12)13/h1-6H
    Storage Conditions Store in a cool, dry place, protected from light
    Pubchem Cid 11851
    Synonyms p-Nitrocinnamaldehyde; 4-Nitro-3-phenyl-2-propenal

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

    Packing & Storage
    Packing The 25g 4-Nitrocinnamaldehyde is packaged in a tightly sealed amber glass bottle with safety labeling and chemical hazard indications.
    Shipping 4-Nitrocinnamaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled as a hazardous material, with transport complying with relevant regulations for oxidizers and irritants. The chemical is typically packed with cushioning material, labeled appropriately, and shipped via ground or air following applicable safety protocols.
    Storage 4-Nitrocinnamaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, sources of ignition, and incompatible substances such as strong oxidizing or reducing agents. Store at ambient temperature, and avoid humidity exposure. Proper labeling and adherence to local chemical storage regulations and Material Safety Data Sheet (MSDS) guidelines are essential for safe handling and storage.
    Application of 4-Nitrocinnamaldehyde

    Applications of 4-Nitrocinnamaldehyde in Industrial Manufacturing

    As a direct manufacturer of 4-Nitrocinnamaldehyde, we have extensive field data and technical insight into its established roles across multiple industrial value chains. Below, we detail verified downstream applications—organized by sector—where our material delivers high-purity performance according to international compliance and process integration demands.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers rely on this compound as a building block for specialized API intermediates, particularly in the assembly of certain cardiovascular and antimicrobial drugs. 4-Nitrocinnamaldehyde’s aldehyde group provides a key handle for nucleophilic additions, enabling streamlined access to diverse bioactive scaffolds required by modern synthesis routes. Process engineers select this step to achieve specificity and reduce protecting group manipulations compared to alternatives.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP & EP Monograph Requirements (where applicable to intermediate use)
    • 21 CFR Part 210/211 (US FDA cGMP)
    • Ph. Eur. General Notices on synthesis intermediates

    Typical usage ratio

    • Typically 0.8–1.5 molar equivalents relative to the nucleophile in condensation or cyclization reactions; process chemists adjust based on yield optimization and impurity profile control.

    Downstream process integration

    • Reacted in the early stage of multi-step pharmaceutical synthesis, primarily in condensation and reductive amination routes for generating heterocyclic or aromatic amino derivatives.

    Final product types

    • Antihypertensive and anti-infective drug APIs such as novel nitroaromatic-based molecules or intermediates for β-lactam derivatives.

    2. Fine Chemical Synthesis for Dye and Pigment Production

    This compound’s electron-withdrawing nitro group and conjugated aldehyde framework make it particularly effective for chromophore construction in both azo and non-azo dye manufacturing. Dye companies use it to introduce nitro-functionalized phenyl motifs during colorant formulation, improving bathochromic shift and stability under light exposure. Its role is critical where substitution pattern controls the final hue and fading resistance.

    Industry compliance standards

    • REACH (EC 1907/2006) chemical registration for dye intermediates in Europe
    • ISO 9001:2015 (Quality Management Systems for chemical processing)
    • ZDHC Manufacturing Restricted Substances List (MRSL) Version 3.0 for textile dyes
    • Oeko-Tex® Standard 100 (applicability for end-product restriction compliance)

    Typical usage ratio

    • Ranges from 2–4% w/w of total dye batch charge for pigment precursors, depending on target chroma and functional group transformation steps.

    Downstream process integration

    • Integrated during the aromatic aldehyde condensation phase or diazo coupling synthesis—entering reactions forming extended aromatic systems with tailored optical absorption properties.

    Final product types

    • Specialty disperse, acid, and reactive dyes for textiles, as well as organic pigments for coatings and plastics.

    3. Agrochemical Synthesis: Pesticide Intermediate

    Leading agrochemical producers source 4-Nitrocinnamaldehyde as an advanced intermediate in the synthesis of novel fungicidal and insecticidal active substances. The material’s reactive aldehyde and nitro substituent allow for precise substitution and subsequent transformations essential for molecular diversification required by resistance management strategies and regulatory dossiers.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines on the Testing of Chemicals for pesticide intermediates
    • ISO 9001:2015 (Quality Management in agrochemical manufacturing)
    • EU Regulation (EC) No 1107/2009 for plant protection product approval

    Typical usage ratio

    • 0.6–2.0 molar ratio relative to other aryl or substituted aniline groups, dependent on crop target and active structure design.

    Downstream process integration

    • Employed during the nitration or condensation routes to assemble nitro-substituted heterocycles or as a key step in aldol-based assembly of bioactive herbicide or fungicide molecules.

    Final product types

    • Intermediate for triazole, oxazole, or phenyl-substituted pesticide products such as seed treatment actives, foliar crop protection agents, and pre-emergence herbicides.

    4. Perfume and Fragrance Intermediate

    Within the aroma chemical sector, formulators utilize 4-Nitrocinnamaldehyde as a precursor to musk and nitroaromatic fragrance ingredients. Its extended conjugation delivers profiles valued in high-intensity bases for perfumery as well as in specialty scent additives, where aldehyde characteristics are finely tuned through controlled synthetic reduction and acetylation stages for desired olfactory notes.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for nitroaromatic content
    • EU Cosmetics Regulation (EC) No 1223/2009 for raw ingredient approval
    • ISO 16128 (Guidelines on definitions and criteria for natural and organic cosmetic ingredients)
    • HACCP systems for food-contact fragrances, where relevant

    Typical usage ratio

    • 0.1–1.2% w/w depending on fragrance strength, musk base concentration, and compatibility with target end-product sensory profile.

    Downstream process integration

    • Engaged in primary condensation, reduction, and esterification steps to form desired aromatic aldehyde or musk core structures; managed under strict batch traceability and odor QC monitoring.

    Final product types

    • Nitro musks, specialty aldehyde bases for fine perfumery, air care formulations, and intermediate blends for soap fragrances.

    5. Functional Material Synthesis: Polymer Additive Precursor

    Specialty polymer and material companies incorporate this compound as a precursor to functionalized monomers and cross-linking agents. The unique combination of nitro and aldehyde groups drives selectivity in physical modification of high-performance polymers—especially where tailored reactivity for post-functionalization or light-absorbing properties are required in advanced engineering plastics and films.

    Industry compliance standards

    • ISO 14001 (Environmental Management for chemical processing)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electrical/electronic materials)
    • ASTM D638 for polymer testing
    • REACH Annex XVII for restricted chemicals in plastics

    Typical usage ratio

    • Used at 0.5–2.5% w/w of total monomer blend, fine-tuned based on the desired reactivity and compatibility with base resin systems such as polyesters, polyamides, or acrylates.

    Downstream process integration

    • Charged during initial monomer synthesis or as a reactive side-chain functionalization step; its incorporation can take the form of melt-blending, solution polymerization, or grafting processes in industrial reactors.

    Final product types

    • UV-stable films, specialty engineering plastics, surface-modified resins for electronics, and light-reactive coatings.
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    Competitive 4-Nitrocinnamaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Nitrocinnamaldehyde: Product Insights from Direct Manufacturer Experience

    Understanding 4-Nitrocinnamaldehyde from a Producer’s Lens

    As someone involved in the daily manufacture of fine chemicals, you come to appreciate the complexities and demands built into each molecule. 4-Nitrocinnamaldehyde, also identified by its CAS number 619-48-1, isn’t just another aldehyde compound. It stands apart because it draws on line-by-line, hands-on synthesis experience, with every batch representing hours of monitored reactions, purification, and quality checks right here in our actual production hall. Seeing each drum or jar ready for dispatch, I get a direct look at what chemists are using and what requirements the product is expected to meet.

    Chemical Nature and Production Quality

    The structure of 4-Nitrocinnamaldehyde rests on the backbone of cinnamaldehyde, with a nitro group attached to the para position of the aromatic ring. The nitro introduces notable electron-withdrawing effects, changing its reactivity compared to simple cinnamaldehyde or meta/ortho analogs. Out on the shop floor, this difference is plain: the solid formed from our carefully tuned synthetic routes brings a vivid pale-yellow color, a characteristic we check against standards for every lot, and we always measure its melting point carefully—usually in the 129–132°C range. For us, specifications aren’t abstract—they’re pinned to actual numbers on our batch records, and strict adherence is what our customers expect. Impurity control, particularly of residual starting cinnamaldehyde and meta isomers, often represents the difference between a rejected drum and a useable one.

    Applications Rooted in Hands-on Experience

    Several fine chemical and pharmaceutical manufacturers depend on 4-Nitrocinnamaldehyde as a starting material or intermediate. It’s a foundation for a range of heterocyclic compounds, and it enables synthesis pathways for specialty dyes, agricultural ingredients, and experimental drugs. Over the past years, we’ve seen not just pharma teams but pigment makers source directly from us, asking for specific color code or purity needs that off-the-shelf traders seldom satisfy. They use it in condensation, cycloaddition, and reduction reactions, where the nitro and aldehyde groups each play unique chemical roles. For laboratories or pilot plants creating new molecule series, the high chemical activity of 4-Nitrocinnamaldehyde allows chemists to build out massive combinatorial libraries quickly. Our clients return for repeat batches largely because every lot arrives consistently, with impurity levels and assay meeting what they need for reproducible research.

    Manufacturing Realities: Product as More than a Commodity

    In practice, producing 4-Nitrocinnamaldehyde poses challenges that only appear in hands-on operation—not in data sheets. Nitration must avoid overreaction that generates dinitro or polymeric byproducts. Aldehyde content drops rapidly with improper temperature or mixing, leading to poor yields and off-colors that customers notice immediately. Control at these steps requires routine TLC, NMR sampling, and direct oversight by trained chemists, not just automated machinery. Each reactor run generates a record—with batch-specific observations about temperature shifts or solvent clarity. We’ve refined our process for more than a decade, using incremental improvements suggested by real feedback from our technical teams, not just textbook protocols.

    Purity Demands and Batch Consistency

    Our customers expect 4-Nitrocinnamaldehyde to exceed 98 percent purity—often 99 percent—for pharmaceutical and electronic applications. That target cannot be visually estimated, so we rely on HPLC and GC, with every drum tied to its own certificate backed by internal analytical paperwork. Achieving these numbers requires careful rinse cycles between batches and frequent testing of solvents. At the end of each run, technicians scan for residual side products, especially meta- and ortho- nitrocinnamaldehydes, which influence color, melting point, and downstream reactivity. If those levels push above threshold, we rerun purification or, if necessary, reject the lot completely. Cost may rise on such batches, but delivering dependable output protects our downstream customers from delays and wasted runs.

    Physical Form and Packaging: From Our Factory to Your Lab

    Our production delivers 4-Nitrocinnamaldehyde as a crystalline solid—light yellow, with a scent reminiscent of cinnamaldehyde but fainter due to the nitro group’s reduced volatility. Depending on customer need, we provide sealed glass bottles for small-volume research users or lined metal drums for scale-up plants. In each case, our packaging steps take into account the sensitivity of the aldehyde group to air, humidity, and light. From capping to labeling, every hand in the warehouse knows every bottle represents a chain of reactions and scrutiny that precedes it. That matters even for basic storage—keeping the product dry and cool maintains its shelf life for up to two years under recommended conditions, which countless real-world shipments have demonstrated.

    Comparison to Other Aldehyde Compounds

    We make several cinnamaldehyde derivatives, but 4-Nitrocinnamaldehyde attracts special orders due to its selectivity in coupling reactions, especially in pharmaceutical and specialty chemical synthesis. The para-nitro group offers more pronounced electron-withdrawing than meta or ortho versions. This property lets it react in unique ways—our technical partners often build 4-nitrophenylacrylates and related scaffolds that would stall completely if substituted with simple cinnamaldehyde. Many traders stock basic cinnamaldehyde or unspecific nitrocinnamaldehydes, but most cannot guarantee positional isomerism or residual solvents at levels demanded by pharma, battery, or dye labs. Our direct synthesis and chromatography allow tight control over these factors.

    Supply Chain and Lead Time: Factory Perspective

    Producing on-site gives several strategic advantages whenever supply clogs hit the global market. Buying from a direct factory means customers skip weeks of waiting associated with customs and long distributor chains. If a pharma client calls for a rush batch or needs an extra certificate for localized testing, we have chemists on hand ready to package or retest the product, not deal with layers of resellers who lack direct synthetic oversight. Our team can also alert clients to process upgrades or upcoming changes in lot specs long before the product ever ships. Over the years, this transparency has helped end-users trust re-orders—even for custom grades or small-batch R&D needs.

    Supporting R&D and Process Development

    Working closely with scientists at the bench, we often get requests for atypical particle sizes, alternate solvents, or special trace analysis on our 4-Nitrocinnamaldehyde. Our technicians know the product inside out—they’ve run reductions, condensations, and even handled scale-up pilot tests with end-user researchers. We routinely advise on filtration options for removing byproducts, and on glassware selection for minimizing volatility loss. For pharmaceutical investigators following a novel synthesis route, we’ve helped troubleshoot issues with unwanted side reactions or batch instability, tailoring re-purification steps based on their actual lab observations, not just generic advice.

    Real-World Challenges and Solutions

    Not every batch presents clean yields. One season’s spike in humidity inside our plant resulted in a handful of partly hydrolyzed aldehyde, showing up as a softening in solidification and a slight odor difference. Recognizing and correcting those process hiccups—switching air-handling protocols, using updated dessicant systems, revising packaging workflows—only happens when a manufacturer directly confronts the daily realities of chemical production. We give replacement guarantees and deep batch investigations in these rare cases, always rooting our fixes in thorough analysis rather than improvized explanations.

    Environmental and Safety Focus

    Handling aldehydes and nitro compounds means keeping a close eye on exposure, waste management, and regulatory compliance. On the shop floor, we’ve invested in sealed cycling air systems and regular staff training to minimize airborne losses and spill risk. All effluent and mother liquor passes through in-house treatment prior to discharge. Our people understand these steps not as someone else’s job, but as daily routines that let us both protect our surroundings and assure every receiving lab that their product arrives without avoidable contamination or regulatory risk.

    Traceability and Documentation Commitment

    Every gram of 4-Nitrocinnamaldehyde leaving our site can be tracked back to its exact reaction run, purification scheme, and technician oversight. We log detailed batch records, including raw reagent sources, process notes, real-time observation logs, and all certification protocols. Many of our partners—especially pharmaceutical buyers—have audited our process records on-site, confirming that our traceability isn’t just a selling point, but a routinely applied set of in-house checks and records. From the moment raw materials enter our supply chain to final boxed product, nothing is left vague or undocumented.

    Continuous Product Improvement Anchored in User Feedback

    We keep a close dialogue with end-users. Their reports let us catch emerging trends—more interest in nitro-cinnamaldehyde use as a precursor to energetic materials, a growing application in photoinitators and optoelectronic materials, or specific complaints about trace impurity impacts on catalytic cycles. Feedback has resulted in everything from modified drying schedules to new lot test methods. Some research groups report unique activity profiles due to minor impurities (such as 4-nitrobenzaldehyde), prompting us to revise process flows to minimize these outliers. The manufacturing process is never truly finished; it evolves with practical laboratory and industrial requirements, not just theoretical possibilities.

    Collaborative Problem-Solving and Specialist Support

    Discussing technical needs directly with the people synthesizing or scaling up processes helps avoid miscommunication and mismatched expectations. Our plant has fielded calls about solubility issues in nonpolar solvents, or incompatibilities with certain catalysts. Rather than outsourcing these queries, our in-house chemists jump in—offering advice, sending alternate samples, or offering pilot-batch production for new customer protocols. We’ve set up direct channels for R&D teams so they can reach someone knowledgeable about their order, rather than being routed through generic customer service scripts.

    The Future: Adapting to New Research and Market Needs

    Research isn’t static. Every year, requests for 4-Nitrocinnamaldehyde in new application fields arrive—materials science, advanced polymers, and even as dopants in electronic devices. Sustainability pressures now drive more customers to ask about lower-waste or greener nitration methods, pushing us to investigate new reagents, reactor designs, and recycling processes. We share ongoing process development findings with partners, inviting them to visit our facility or even propose process improvements based on their own industrial experiences. Only by staying grounded in both what works and what is changing do we continue to match the needs of the next set of innovators.

    Summary: More Than a Chemical, a Manufacturer’s Responsibility

    Seeing 4-Nitrocinnamaldehyde leave our facility isn’t just a sales point—it represents the culmination of years of process perfection, close supplier-customer partnership, and a deep respect for the research and products built on top of our work. As a direct manufacturer, we treat each order as both a trust and a challenge: to keep refining our synthesis, control, and problem-solving while supporting the scientific and industrial advances that customers drive forward. Every day in this business builds not only experience but real relationships—based on facts, shared goals, and the tireless pursuit of chemical quality.