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3-Nitrovalerophenone

    • Product Name 3-Nitrovalerophenone
    • Alias 1-(3-Nitrophenyl)pentan-1-one
    • Einecs 220-561-1
    • 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
    VTB
    Specifications

    HS Code

    831718

    Chemical Name 3-Nitrovalerophenone
    Cas Number 50915-13-8
    Molecular Formula C11H13NO3
    Molecular Weight 207.23 g/mol
    Appearance Pale yellow solid
    Melting Point 38-40 °C
    Density Unavailable
    Solubility Soluble in organic solvents
    Smiles CCCCC(=O)C1=CC=CC=C1[N+](=O)[O-]
    Inchi Key JADCNHGBOYHLJE-UHFFFAOYSA-N
    Pubchem Cid 175385
    Refractive Index Unavailable

    As an accredited 3-Nitrovalerophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tightly sealed cap, featuring a white label displaying “3-Nitrovalerophenone, 25g, for laboratory use only.”
    Shipping 3-Nitrovalerophenone is shipped as a chemical substance, typically in tightly sealed containers to prevent exposure to moisture and air. It should be packed in accordance with relevant hazardous material regulations, including clear labeling. Transport must comply with local and international safety guidelines to ensure proper handling and environmental protection.
    Storage 3-Nitrovalerophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible materials such as strong oxidizers and reducing agents. Store in a designated chemical storage area, clearly labeled, and ensure proper secondary containment to prevent spills or leaks.
    Application of 3-Nitrovalerophenone

    Applications of 3-Nitrovalerophenone in Industrial Manufacturing

    As a specialist manufacturer of 3-Nitrovalerophenone, we support a range of advanced synthesis pathways and specialty intermediate requirements across chemical industries. Our material achieves consistent quality demanded by regulated manufacturing sectors, and integrates directly into multi-step production lines for value-added end-use products.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies rely on 3-Nitrovalerophenone as a key intermediate in the synthesis of certain regulated APIs, notably within the anticonvulsant and CNS-active product pipeline. The compound enters localized nitration and coupling processes to deliver substituted benzophenones, essential for further modification under controlled conditions. Downstream formulators must validate every batch against stringent impurity profiles and maintain documentation for full process traceability.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for intermediates
    • U.S. Food and Drug Administration (FDA) 21 CFR Part 210/211 (cGMP for finished pharmaceuticals)
    • APIC Guidelines for API manufacturing

    Typical usage ratio

    • Used at 1–15% molar basis relative to target API, depending on process yield and pathway, with adjustments for reaction scalability in pilot and commercial plants

    Downstream process integration

    • Introduced in initial ketone nitration and subsequent reductive amination or condensation steps during multi-stage API manufacturing

    Final product types

    • Anticonvulsant drug substances
    • Custom CNS-active molecule precursors
    • Intermediates for generic pharmaceutical development
    • Bulk intermediates for global ANDA supply chains

    2. Agrochemical Intermediate Production

    Companies manufacturing high-value crop protection chemicals utilize our material as an intermediate in the formation of certain functionalized ketone derivatives. The nitro group supports selective reactivity during successive transformations, such as acylation and subsequent cyclization, to access herbicide or fungicide backbone molecules. Strict handling and full batch reconciliation are standard requirements for plant operators due to the downstream impact on active ingredient quality.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP), applicable to product development
    • FAO and WHO International Code of Conduct on Pesticide Management
    • ECHA Regulation (EC) No 1907/2006 (REACH) for industrial chemical substances
    • ISO 9001:2015 for chemical manufacturing quality control

    Typical usage ratio

    • Input at 3–10% by weight in batch synthesis, varied by direct transformation stage and final yield demands

    Downstream process integration

    • Feeds into cyclization, alkylation, and reduction processes as a protected precursor supplying the nitro functionality

    Final product types

    • Precursors for selective herbicides
    • Fungicide intermediate streams
    • Key reagents for seed treatment active development
    • Industrial protection agent intermediates

    3. Fine Chemical Intermediates for Fragrance Synthesis

    Manufacturers in aroma chemicals and fine fragrances integrate this ketone intermediate for the construction of complex fragrance molecules, particularly those requiring controlled insertion of aromatic nitro groups. The material allows precise ketone modification by acylation or reduction employed in the synthesis of musk analogues and tonalide derivatives. Processing requires validated purity and minimal residual solvents to comply with finished product standards.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for ingredient purity
    • Good Manufacturing Practice (GMP) for Cosmetic Ingredients (ISO 22716)
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • REACH Annex XVII restrictions for nitro compounds

    Typical usage ratio

    • 0.5–8% w/w by reaction batch, dependent on target fragrance structure and route specifics

    Downstream process integration

    • Utilized in stepwise acylation or condensation reactions to generate macrocyclic musk analogues or precursor alcohols following controlled reduction

    Final product types

    • Fragrance intermediates (e.g., musk ketones)
    • Specialty aroma blends for perfumery bases
    • Precursors for top-note aldehyde syntheses
    • Tonality enhancers in commercial fragrances

    4. Specialty Polymer Additive Synthesis

    Polymer and resin industry clients employ 3-Nitrovalerophenone in the development of nitro-functional resin additives. Its integration supports improved chemical reactivity and targeted properties such as UV stability, tint retention, and cross-linking efficiency. Exact proportioning aligns with polymer chain lengths and desired additive loading, with regular QC validation for homogeneity and absence of unreacted nitro species.

    Industry compliance standards

    • ASTM D2567 (Standard Practice for Laboratory Evaluation of Additive Effects in Plastics)
    • ISO 9001:2015 for additive manufacturing
    • RoHS Directive 2011/65/EU for electronic polymers
    • FDA 21 CFR 177 for allowable polymer additives in indirect food contact materials (where applicable)

    Typical usage ratio

    • Used at 0.1–1.5% by weight of polymer matrix, adjusted according to additive function and compatibility testing

    Downstream process integration

    • Employed during pre-polymer blending or as part of post-polymerization modification to introduce functionality prior to extrusion or molding

    Final product types

    • UV-stable resin formulations for automotive coatings
    • Functional masterbatches for specialty plastics
    • Cross-linkable polymer compounds in adhesives
    • Performance additive formulations for construction sealants
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    Certification & Compliance
    More Introduction

    Introducing 3-Nitrovalerophenone: Perspective from a Chemical Manufacturer

    Real-World Manufacturing Experience with 3-Nitrovalerophenone

    Every day in the plant, as we monitor reactor temperatures and fine-tune our purification systems, we see the value that compounds like 3-Nitrovalerophenone bring to modern synthesis. Our history with this intermediate goes back more than a decade, and during this time, we've worked through the kind of challenges only those with their own reactors and distillation lines truly appreciate. There is only so much theory someone can study before putting on gloves and goggles, weighing out raw materials, and watching the exotherm on a nitroalkylation reaction.

    3-Nitrovalerophenone, with the systematic designation of 1-(3-nitrophenyl)pentan-1-one, fills a specialized but critical niche in the world of advanced intermediates. The chemical structure—essentially a valerophenone core carrying a nitro group at the third position—gives it unique reactivity that chemists look for when planning downstream transformations. Quality in manufacturing here starts from the choice of starting benzene ring, the integrity of pentanoyl chloride sourcing, efficient nitration under controlled conditions, and, not least, a well-documented purification process.

    Specifications Matter—Here’s Where Experience Pays Off

    Anyone can order a catalog product with the right registry number. Producing a kilo and scaling up to batch after batch at drum scale require rigor in checkpoint analysis and repetition of the same quality every time. On our lines, 3-Nitrovalerophenone comes out with a consistent purity profile, commonly above 98%, verified through GC-MS and HPLC. Impurities, particularly unreacted aldehydes or positional isomers, are minimized by close process controls and repeated quality assurance. Melting point, appearance (usually pale yellow to light brown crystalline solid), and moisture content fall within tight, experienced batches rarely fail to meet customer benchmarks.

    Separator columns and crystallization tanks don’t care much about impressing a spec sheet; they deliver purity by thorough washing and smart process design. We’ve learned that running reactions too hot leads to byproducts, while cutting corners on the extraction phase risks increased isomeric contamination. Over hundreds of runs, our team has traced how even a one-degree fluctuation on a jacketed reactor can shift impurity profiles. Only a team that does the work day in and day out can know these details by heart.

    What Sets 3-Nitrovalerophenone Apart

    Not all nitro ketones behave the same or offer the same synthetic utility. In our operations and feedback from partner labs, 3-Nitrovalerophenone stands out because the nitro group at the meta position balances electron-withdrawing effect with aromatic substitution patterns favorable for downstream chemistry. The pentyl side chain resists rapid hydrolysis or over-alkylation, giving researchers greater control in multi-step syntheses. Where other nitrophenones tend toward instability or unpredictability, this structure holds up well under a variety of reaction conditions—from reduction to reductive amination, or as a scaffold in complex pharmaceutical development.

    Manufacturers with surface-level experience often ship material with excessive odor, dark color, or trace solvent residues. We see the difference on our own HPLC graphs and customer feedback forms. High-quality 3-Nitrovalerophenone enters the market with minimal background noise in spectra, and its melting range sits reliably tight, leading to less variation in subsequent transformations.

    Usage: Real Applications Driving Demand

    From an industrial and laboratory point of view, demand for 3-Nitrovalerophenone tracks most closely with research and commercial projects in pharmaceuticals, advanced materials, and agricultural science. Our largest customers—a mix of global pharma companies and specialized research firms—rely on it as a starting material or intermediate. One typical use involves catalytic hydrogenation to produce amines for further cyclization. Reduction or substitution reactions take full advantage of the activated aromatic system and nearby functional groups. This effectiveness comes from the combination of its stable core and the electron-deficient nitro site.

    Feedback from medicinal chemistry teams highlights how the compound can act as a scaffold for building out heterocycles, benzodiazepine precursors, or substituted anilines. Large-scale users push for consistent, impurity-free supply, knowing that even trace byproducts complicate their purification and reduce process yields downstream. Our operators often note that demand spikes around new pharmaceutical scaffold research, and we see patterns where academic interest follows announcements of newly patented treatments or novel inhibitors. Nobody is pulling from a theoretical catalog—these are hands-on synthetic programs.

    Having supplied multi-kilo shipments worldwide, we’ve learned the logistical and technical headaches that come when a batch arrives out of spec. Every drum leaving our site traces back through a transparent chain of data logs. From in-process TLC monitoring to final certificate of analysis, every step is archived. This traceability gives our buyers—who have seen enough failed projects to know better—practical assurance their synthesis won’t bottleneck on poor raw materials.

    Comparison with Other Nitro Ketones and Phenones

    Plenty of chemicals fight for a spot as an intermediate or substrate in advanced synthesis pipelines. The market features diverse nitro phenones—ortho, para, and various side chains with short or branched alkyl groups. Our own teams have worked with para-nitro derivatives and other chain lengths over dozens of campaigns. Some customers compare 3-Nitrovalerophenone directly with 4-nitroacetophenone or similar aryl ketones and find that substituted position and chain length determine downstream reactivity more than minor sourcing differences.

    Ortho-substituted nitro ketones often present issues—unwanted steric strain or altered reactivity that makes controlling reduction or nucleophilic additions more difficult. Para-substituted nitro phenones have a role, usually where a less hindered phenyl ring is necessary, but they display significant electronic effects unsuited for every route. 3-Nitrovalerophenone, with its meta nitro functionality, bridges a gap in modulating electron density without undue steric luxury or withdrawal. That subtlety often means improved selectivity in reduction steps or cross-coupling operations.

    Chain length matters. Shorter ketones, like the acetophenone derivatives, may undergo side reactions too readily or degrade under prolonged reaction times. Heavier chains risk solubility issues, especially in scale-up operations, and can reduce reactivity. Our ongoing conversations with users in the field confirm this: valerophenone’s five-carbon backbone balances reactivity with ease of handling, making it versatile for both bench and plant settings.

    Over the years, we noticed researchers gravitate toward 3-Nitrovalerophenone for reactions where they sought a compromise between reactivity, stability, and manageable processing hazards. That middle ground rarely comes from consulting catalogs, and is born out of long, practical experience.

    Quality Assurance Never Stops

    In our industry, trust is as critical as the molecules themselves. We learned it the hard way early on: inconsistent batches, unfiltered solvents, or insensitive packing materials cost credibility overnight. Whether it’s the batch records, the color check under standardized lighting, or the residual solvent limits so strict we double-check by GC-FID, quality assurance lives and breathes on the manufacturing floor.

    We keep every sample from every lot until well after the last kilogram ships. That habit started from customer requests, then turned into standard operating procedure. Years ago, a client flagged a downstream crystallization issue. By holding back reference material and full process data, our technical team found a slight solvent overlap missed in earlier detection. Since then, cross-verification happens on every finished batch, including fresh equipment calibrations and third-party lab confirmation for some key parameters.

    Every kilogram of 3-Nitrovalerophenone we ship leaves our plant with a batch-specific certificate confirming identity, purity, moisture, and critical residuals. Our analytical reports don’t get buried in admin—it’s daily reading for anyone on shift. Quality for us is less about hitting a line on an external audit and more about repeat performance for the people relying on this intermediate at the sharp end of their own production.

    Sustainability and Safety in Every Batch

    For years, safety and environmental impact have shaped how we run the plant and commit to new process improvements. Nitration reactions need careful management; uncontrolled byproduct formation or improper venting create environmental risks no responsible manufacturer ignores. We run extra safety layers—automated temperature and pressure monitoring, gas scrubbers, and water treatment. Employees train weekly on both normal operations and what to do should a sensor flag an off-normal state.

    We pursued closed-loop solvent recovery years before it became an industry buzzword. Ethyl acetate, once treated as a disposable consumable, now runs through a return and repurification setup we installed after a run of shortages. Not only do these changes reduce costs, but they sharply lower emissions and align with expectations from the kind of clients who audit us for supply chain sustainability. Every kilo of 3-Nitrovalerophenone that leaves our site reflects this investment, from procurement through to safe packaging and logistics.

    Operating in this market brings regulatory scrutiny—rightly so. Nitroaromatic compounds have historical baggage, even if current uses are legitimate and well controlled. We comply with regional handling, storage, labeling, and transport rules, making sure nothing leaves our gate without accurate paperwork. That focus includes ongoing internal checks, employee training, and regularly updated safety data sheets tailored for both plant operators and downstream users.

    Practical Challenges and Solutions from the Ground Up

    Producing 3-Nitrovalerophenone at commercial scale brings plenty of challenges, some foreseeable, others only obvious with time on the plant floor. One constant issue: dust generation during powder handling. Nitro ketones in particular tend to develop static cling, risking both product loss and operator discomfort. We invested in improved antistatic equipment and modified our packaging workflow to reduce airborne dust. While equipment suppliers talk about theoretical flow rates and anti-static liners, we put in overtime tracking actual product losses during each manual transfer.

    Another frequent challenge: balancing throughput with purity. Early on, push for higher batch volumes led to lower quality product, with more color bodies and heavier odor. Scaling up wasn’t just a matter of using bigger reactors or harder agitation—it took process mapping, better filtration, and iterative design of washing and separation steps. Polymer engineers helped us refine gasket material to prevent subtle solvent leaching, which mattered a lot more than most off-the-shelf setups allow.

    Shipment logistics, especially for export-bound lots, never stays simple either. Nitroaromatics fall under additional hazardous materials transport rules, so we built up relationships with specialized carriers, increased internal documentation, and fine-tuned both outer drum packaging and labeling for each target region. Speed doesn’t trump compliance when regulatory inspections can cost a shipment and the relationship with long-term customers.

    Clear communication and nimble adjustments remain powerful tools. End users don’t just buy purity numbers; they buy reliability, traceability, and open doors to technical dialogue on unexpected issues. Our technical teams resolve a range of user queries—whether about unexpected side reactions, re-purification, or process troubleshooting—because we know the value of after-sales support.

    Continuous Improvement Driven by Real-World Demand

    Every new customer requirement tightens our process: higher purity, tailored particle size, or faster documentation turnaround. Years of manufacturing have cemented the importance of investing in both staff skills and smarter tools. Our plant now runs automated recipe uploads, real-time process analytics, and digital inventory controls linked directly to the QA lab. These upgrades took time, but the payback comes through fewer errors, tighter control, and faster response when things don’t go as planned.

    Supplier integrity matters as much as internal diligence. We work only with long-term vendors who provide clean, traceable precursors and ship on spec—no cut corners or mystery blends. That’s a commitment rooted in repeated field experience: every shortcut upstream risks a costlier failure in our own lines. Vendor audits, regular scorecards, and fast-track problem correction all fit into keeping 3-Nitrovalerophenone flowing to customers no matter the market shortage.

    Employee safety remains non-negotiable. Every plant shift ends with cleanup and maintenance work, supported by real-world, up-to-date training. Bad habits—like improper PPE or shortcutting a filtration step—get flagged and corrected immediately. This isn’t just risk management, it’s smart business: healthy operators mean consistent throughput, lower downtime, and safer, cleaner products.

    Invested in the Future: Evolving with Application Needs

    3-Nitrovalerophenone’s value in the industry comes from blending chemical insight with on-the-ground adaptation. Over the years, as new research and commercial applications shift, we reinvest in process development, scaling techniques, and customer collaborations. We pay attention to customer synthesis goals, adapting product purity or particle size as needed and providing detailed data to support them.

    Advanced applications like targeted pharmaceuticals or specialty agrochemicals push up requirements. Analytical techniques have shifted, with more end users requesting trace-level impurity data or tailored safety documentation. Our laboratories add methods right along with these requests, expanding both our understanding and the quality of data that support each shipment.

    We remain committed to tightening controls, from energy use to solvent waste. Our facility planners invest in emissions reduction and resource efficiency—not just for compliance but for long-term cost savings and customer confidence. Energy-efficient process heaters, LED retrofits, and water re-use systems may seem like small steps, but over time, these shape the sustainability and integrity of every gram we deliver.

    Enduring Partnerships, Built on Trust and Expertise

    Being a manufacturer of 3-Nitrovalerophenone means more than filling orders. It means listening to customer feedback, keeping pace with industrial innovation, and investing in plant operations. We know the science because we run the reactors. We know the business because missed deliveries or failed batches cost real relationships. Our commitment to expertise, verifiable quality, and adaptable service is visible with every drum of 3-Nitrovalerophenone that leaves the loading dock.

    Each partnership formed with a customer builds on not just the molecule, but a foundation of technical understanding, proven reliability, and willingness to improve. We learn from every run—whether for a new pharmaceutical, agricultural trial, or specialty material application—and let that experience shape future operations. That’s the promise we make with each kilogram delivered, and the expertise we stand behind every day on the production floor.