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Valerophenone

    • Product Name Valerophenone
    • Einecs 211-881-4
    • 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
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    Specifications

    HS Code

    941606

    Chemical Name Valerophenone
    Cas Number 1009-14-9
    Molecular Formula C11H14O
    Molar Mass 162.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 243-244 °C
    Melting Point -18 °C
    Density 1.008 g/cm³
    Refractive Index 1.519
    Flash Point 96 °C
    Solubility In Water Insoluble
    Synonyms 1-Phenyl-1-pentanone
    Smiles CCCCC(=O)C1=CC=CC=C1
    Pubchem Cid 7515
    Ec Number 213-767-3

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

    Packing & Storage
    Packing Valerophenone is packaged in a 250 mL amber glass bottle with a secure screw cap, labeled with hazard and identification information.
    Shipping Valerophenone should be shipped in accordance with local, national, and international regulations for hazardous chemicals. Use intact, sealed containers, labeled appropriately, and cushioned to prevent breakage. Ship at ambient temperature, away from strong oxidizers and incompatible substances. Ensure transport documentation includes safety and handling information per relevant guidelines such as SDS and UN regulations.
    Storage Valerophenone should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from oxidizing agents and strong acids. Store at room temperature and ensure proper labeling. Use secondary containment to prevent spills, and keep away from incompatible substances to ensure chemical stability and safe handling.
    Application of Valerophenone

    Applications of Valerophenone in Industrial Manufacturing

    As a specialized producer of valerophenone, we supply this key chemical intermediate to various downstream sectors where precision formulation, regulatory adherence, and advanced process control are mandatory. Below are primary industry segments where valerophenone finds practical, verified use, each described by sector-specific technical parameters and product integration requirements.

    1. Photoinitiators for Ultraviolet (UV) Curing Systems

    Valerophenone serves as a core intermediate in manufacturing benzoin-type and other aryl ketone photoinitiators used in advanced UV curing formulations for industrial coatings, inks, and adhesives. Its aromatic ketone structure imparts reliable absorption characteristics and reactivity under UV exposure, making it suited for quick-setting surface treatments in electronics and packaging. Precise control over purity and input ratio ensures efficient crosslinking and adherence to end-user performance standards.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management System
    • RoHS Directive 2011/65/EU (where electronics applications involved)
    • ASTM D7767 for acrylate photopolymer inks and coatings

    Typical usage ratio

    • 0.5–2.5% by weight in formulated photoinitiator blends; actual range adjusted according to substrate, layer thickness, and required cure depth

    Downstream process integration

    • Valerophenone enters as a core reagent in the synthesis step for benzoin alkyl ethers or derivative photoinitiators. Downstream compounders blend the resulting photoinitiator with monomers or oligomers during the premix phase prior to UV lamp or LED curing application.

    Final product types

    • UV-cured wood and plastic coatings
    • Inkjet-printed packaging
    • Microelectronic conformal coatings
    • UV-set industrial adhesives and sealants

    2. Pharmaceutical Synthesis Intermediates

    Organic synthesis operations use valerophenone as an alkylated aromatic building block in multi-step reaction routes for manufacturing certain active pharmaceutical ingredient (API) precursors. Its controlled reactivity supports efficient carbonyl group transformations in regulated environments, playing an essential role in ketone reduction, Grignard, or Friedel–Crafts reactions for medicines where molecular precision is necessary to meet international pharmacopeia requirements.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) monograph specifications for intermediates
    • US Pharmacopeia (USP)
    • EDQM regulatory filings for synthetic intermediates

    Typical usage ratio

    • Input dose typically ranges from 0.1 to 1.0 equivalents relative to main chain substrates, variable based on target molecule and batch scale; stoichiometry adjusted during route development to maximize final API yield while minimizing impurities

    Downstream process integration

    • Valerophenone is introduced during initial condensation or acylation reactions as a carbonyl donor. It participates in closed batch reactors, monitored for conversion rates and residuals, often followed by sequential hydrogenation, cyclization, or functionalization steps leading to the API or advanced intermediate.

    Final product types

    • Pharmaceutical grade API intermediates for nervous system disorders
    • Building blocks for anticonvulsant molecules
    • Intermediates for specialty benzylamines and arylalkylamines
    • Bulk chemical intermediates for contract manufacturing organizations (CMOs)

    3. Agrochemical Active Ingredient Manufacturing

    Agrochemical formulators integrate valerophenone as a synthetic intermediate in the production chain for specific herbicides and grass growth regulators. The robust ketone moiety enables tailored reactivity during ring substitution and reduction steps, supporting the synthesis of active molecular frameworks. Chemical producers must manage stringent traceability and compositional analysis in line with agricultural product registration protocols worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB/T 1604 Pesticide Intermediate Standards
    • OECD Good Laboratory Practice (GLP) for agrochemical ingredients
    • EPA FIFRA (for US agrochemical registration)

    Typical usage ratio

    • Utilized at 1–5% molar ratio relative to target active backbone depending on the complexity of active molecule and conversion efficiency observed in scale-up trials

    Downstream process integration

    • Valerophenone is charged into reactor trains during initial coupling or Friedel–Crafts processes. Subsequent steps include selective hydrogenation or chlorination, purification, and crystallization before blending into technical concentrate or finished formulation.

    Final product types

    • Pre-emergent herbicide AI intermediates
    • Customized grass suppressants for cereal crops
    • Select specialty fungicide synthesis routes
    • Bulk formulated pesticide concentrates for agricultural use

    4. Fragrance and Aroma Chemical Production

    Industrial fragrance blenders use valerophenone as a controlled precursor in the synthesis of select musk and woody aroma molecules. The compound’s reactivity under Friedel–Crafts alkylation supports the formation of longer-chain aromatic ketones, which serve as key components in high-performance fragrance compositions for detergents, personal care, and fine perfumery. Quality control protocols ensure odor profile consistency and the absence of trace impurities that affect end-user acceptance.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9001:2015 Quality Control for Aroma Chemicals
    • RIFM Standard Methods for fragrance safety evaluation

    Typical usage ratio

    • Precursor introduced at 0.2–1.0 mole equivalents for targeted aroma molecule synthesis; final quantity may be refined by GC-MS screening according to batch size and desired olfactory intensity

    Downstream process integration

    • Integrated during initial ketone coupling reaction, followed by hydrogenation or methylation as required by the specific aroma profile. Post-processing includes distillation and headspace purification to isolate the key note component before blending into compound fragrances.

    Final product types

    • Fine fragrance base notes for perfumery
    • Aroma enhancers for laundry detergents
    • Scent additives in personal wash products
    • Concentrated aroma ingredients for flavor and fragrance houses
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    Certification & Compliance
    More Introduction

    Introducing Valerophenone: A Guiding Tool in Laboratory and Industrial Synthesis

    An Experienced Manufacturer’s Perspective on Valerophenone

    For over two decades, the realities of process chemistry, scale-up, and custom synthesis have kept our team at the bench and inside the reactor. With this experience, we know how a single compound can shape the flow of discovery and manufacturing. Valerophenone, known by its structure as 1-Phenyl-1-pentanone and its CAS number 1009-14-9, always brings a versatility to projects, whether they are run in pilot lots or metric tons.

    In our business, pretty spec sheets don’t dictate success. Pure, reliable, and true chemistry does. Valerophenone stands as a dependable intermediate—its behavior inside both R&D glassware and production vessels makes it a regular fixture on our shelves. In our own practice, it has shown a consistency that many other aryl ketones can’t match. Most of our partners in fine chemical synthesis, from agrochemical researchers to fragrance formulators, have leaned on this molecule for its crisp performance and transparent supply chain.

    What Makes Valerophenone Useful in Chemical Synthesis

    Take any reaction that needs a clean ketone backbone, one that won’t add color, odd odors, or unreactive byproducts. Valerophenone’s C10H12O formula brings all the utility of a phenyl ketone, but with a manageable five-carbon sidechain that balances volatility, hydrophobicity, and reactivity. Our technical staff has personally produced a range of quantities, watching its pale, low-viscosity liquid form maintain consistency from drum to bottle to lab beaker. It dissolves smoothly in standard organic solvents like ether, hexane, toluene, and acetonitrile—factors that always matter whether you’re chromatographing an R&D batch or prepping pilot plant reactors.

    Seasoned process chemists know that the right ketone makes all the difference in Grignard reactions, Friedel-Crafts acylations, reductive couplings, and photochemical experiments. Valerophenone accepts alkyl and aryl additions, undergoes predictable reductions, and stays robust through hydrogenation. Much of its stability owes to the positioning of the carbonyl between an aromatic ring and a pentyl group, balancing reactivity without compromising purity.

    The pharmaceutical sector often turns to valerophenone because trusted sources deliver batch-to-batch sameness—color, boiling range, GC purity—so synthetic steps don’t stall. In the fragrance arena, some perfumers exploit valerophenone’s low background scent to support more delicate notes. Plenty of our end-users produce intermediates for flavors, fixatives, or building blocks for more complex aromatics that demand a clean starting ketone.

    Specifications and Quality Built from Real Operations

    Lab curiosity doesn’t translate to manufacturing until consistency can be proven at 20 kilograms or 2000. Our valerophenone production runs reflect this demand for scalability. We monitor each batch by gas chromatography, UV/VIS, and water content (Karl Fischer). The molecule’s boiling point, usually around 244–247°C, ensures low losses under vacuum distillation and fits into standard downstream separation processes. Our purity never drops below 99%, and customers have told us they see the difference in their own workups—fewer side products, easier final QA.

    Storing valerophenone does not challenge most facilities. It handles ambient conditions, resists light exposure, and avoids rapid oxidation. As a liquid, it’s not prone to crystallization, which eliminates bottlenecks in pumping or metering. Our packaging ranges from amber glass for small requests to high-purity HDPE drums with tamper-evident seals for larger orders. By running our own drum fill and QC line, we prevent contamination or off-spec drips.

    Real-World Applications: Learning from Decades in the Field

    We’ve seen valerophenone play prominent roles in compound libraries, medicinal chemistry, and polymer research. Its reliance in setting up cross-coupling reactions for novel APIs or specialty materials cannot be overstated. We’ve supplied valerophenone for companies who take small quantities to validate novel photoinitiator systems and others who scale to multi-tons for polymerization feedstocks. The molecule’s straightforward structure allows it to serve as both target and reference for analytical standards—our customers’ labs use it to calibrate GC-MS instruments, quantify reaction yields, and probe chromatographic separations.

    Many synthetic pathways involving aryl ketones produce unwanted side products. Valerophenone tends to be more resistant to aldol and Cannizzaro side reactions, especially when compared to similar-sized alternatives like benzylacetone or heptanophenone. This helps downstream purification go smoother, cutting solvent use and saving time.

    In the fragrance sector, valerophenone’s subtle backbone provides stability for esters and aldehydes that would otherwise shift over time. Perfumers use it as a base to build more elaborate molecules because it lends little odor of its own. Flavors researchers working on functional analogues or new base notes frequently build from valerophenone using straightforward alkylations and oxidative steps. The pharmaceutical discovery sector routinely selects it for pilot-scale synthetic routes when testing candidate drug fragments.

    How Valerophenone Differs from Other Ketones and Why This Matters

    Every molecule has competition. From the chemist’s perspective, valerophenone competes with acetophenone, propiophenone, and butyrophenone, all of which form the backbone of many industrial and lab synthetic strategies. What sets valerophenone apart is the five-carbon chain—this adds more than a two-carbon extension. It gives higher boiling stability than acetophenone or propiophenone, making it easier to handle in vacuum distillations and less prone to evaporation losses at manufacturing scale.

    Acetophenone and propiophenone both carry more volatility. Their lower boiling points make solvent removal trickier and can limit their utility for longer, higher temperature operations. Butyrophenone resists side reactions but brings a heavier, more sluggish set of physical characteristics, often slowing down stirring and transfer at production scale. Valerophenone occupies a sweet spot—high enough boiling to stay put, low enough viscosity for easy transfers.

    Compared to methylheptyl ketones or hexanophenones, valerophenone provides a practical balance for practitioners who want neither rapid evaporation nor excessively heavy oils. Its physical form simplifies pumping, chilling, and dosing. Side-by-side, we have measured batch purities before and after routine large-scale reductions. Valerophenone consistently stays within specification, without side-chain degradation or aromatic ring loss.

    For chemists formulating new photoinitiator blends, valerophenone’s performance as a hydrogen abstractor stacks up against aryl ketones with shorter side chains. It absorbs UV light robustly above 300 nm, making it a reference compound in photochemical work. This is a proven trait according to photoresearchers in small-lot ink and cured adhesive labs we often supply.

    Practical Considerations for End-Users and Manufacturing Partners

    Our direct experience tells us that questions about a chemical’s traceability and supply risk count as much as laboratory performance. We only source our own raw materials—phenyl acetic acid and pentanoic acid—from vetted partners with transparent QA records. The route, based on Friedel-Crafts acylation, stays under our supervision from start to finish. Every step gets sampled and tracked through in-house analytics.

    Over the years, some customers have asked about impurities—residual solvents, trace colored byproducts, and even odorous contaminants. We’ve dialed in purification, using both vacuum distillation and carbon bleaching to guarantee as colorless a liquid as feasible. These steps ensure there’s no carryover into downstream processes, meaning synthetic or analytical work stays clean.

    Regulatory compliance doesn’t end at our doors. We regularly review each production step against both domestic and international requirements—this includes monitoring environmental discharges, monitoring worker exposure against relevant thresholds, and staying prepared for regulatory reclassifications of aryl ketones. We avoid persistent organic pollutants at every turn, and our packaging program uses only recyclable or fully returnable drums for larger shipments.

    Waste handling is equally important. Our on-site waste reduction program reclaims solvents and distillation heads and tails. These are processed under strict guidelines, keeping our environmental footprint traceable and minimizing landfill outputs. Our plant operators participate in ongoing training to manage spills, exposure, and safe handling.

    Quality Control and Analytical Transparency

    Analytical transparency starts with real, shareable data. Each valerophenone batch leaves our site with chromatograms and spectroscopic traces. We track purity down to the second decimal percent, including GC retention time reports and full-range FTIR scans. These records don’t just satisfy auditors; they let our partners know exactly what’s going into their process vessels and how much is spectroscopically present.

    In our experience, robust analytics cut down troubleshooting time. Should a batch not meet spec—or a client encounters an unexpected result—our technical staff can trace the issue directly back to batch records, supplier shipment details, or in-process control checks. By maintaining this level of traceability for every lot, we’ve avoided costly recalls and downtime for downstream partners.

    We’ve also invested in shelf-life studies, storing our product under both light and dark, ambient and chilled conditions. After up to three years, GC-MS analysis shows main peaks consistent with the parent compound and negligible formation of oxidized byproducts. Reliable data like this supports our partners who rely on advanced notice for production schedules and long-lead inventory planning.

    Supporting Partners with Practical Guidance

    The unique position we have as a manufacturer—owning every batch that leaves the plant—lets us anticipate needs that go beyond data sheets. Our staff routinely answer questions about downstream reactivity, solvent removal, or blending practices. For example, some users ask about solvent compatibility when scaling up conjugate addition reactions. We have hands-on guidance, whether it means adapting vacuum levels or optimizing cooling for high-throughput runs.

    Our technical support is built from firsthand plant and laboratory work, not sales copy. If a partner faces a reactivity concern or requires technical troubleshooting, we provide suggestions grounded in actual production experience. Whether the issue is a phase separation, unexpected color, or analytical challenge, we communicate solutions tested and proven in our own operations.

    For startups, universities, and innovation centers, we also share practical safety advice. Valerophenone transports and stores much like other light aromatic ketones—no unusual shipping hazards, and a flash point of about 105°C. Our team has refined SOPs over years of safe handling and can share spill containment and PPE procedures specific to this product. This lets smaller labs onboard the compound with confidence and minimize potential disruption.

    Continuous Improvement Driven by Feedback and Regulatory Trends

    We never stand still. Our process group reviews customer feedback every quarter, looking for key improvement areas in both manufacturing and packaging. Recent upgrades include a switch to solvent-free purification, batch-coded drum labeling, and automated trace contaminant testing. These changes grew out of direct suggestions from users who noticed minor inconsistencies or asked for easier batch reference in large projects.

    The fine chemical marketplace also evolves. Over the past decade, regulatory agencies have kept a close eye on aryl ketone production, limiting permissible impurity profiles and updating REACH, TSCA, and other registration requirements. Our regulatory and QA staff stay engaged with industry groups and adapt our documentation and internal controls to comply with changing standards.

    For clients exporting finished products, we offer certificates including traceability statements to accelerate audit processes. This makes customs, third-party certifications, or regulatory audit cycles more efficient for everyone in the supply chain.

    Building Trust with Practical Experience

    What we offer with valerophenone comes from working knowledge—hard-earned from years managing everything from glass-lined reactors to all-steel continuous processes. Real data and steady results encourage repeat orders, but trust takes more. Our policy has always been to share operational lessons, reactivity tips, and storage best practices right alongside every order. If a customer hits an unexpected roadblock, we step up with practical solutions, not just formal paperwork.

    We know that direct manufacturer-supplied valerophenone means reliability. Batch dates, QA protocols, and packaging integrity all speak to a focus on consistent, reproducible material. Without these controls, the risk of third-party adulteration or mislabeling always rises.

    Feedback from users—whether on purity, packaging, analytical support, or technical troubleshooting—is not just helpful, it keeps us improving. Big and small customers alike count on us, because we produce what we supply. The knowledge we pass on often shortens others’ development time, reduces unnecessary experiments, and saves downstream resources.

    Future Opportunities and Responsive Solutions

    Chemistry never stays static. New uses for valerophenone continue to surface—be it as a synthetic handle for smart materials, a building block for specialty pharmaceutical fragments, or a reference compound in advanced detection systems. Our R&D teams constantly test new routes and possible upgrades to our current synthesis. Each batch informs the next, so our clients get the benefit of lessons learned and efficiencies gained.

    We actively collaborate with partners developing novel reaction pathways. Custom grades—tighter specification, unique solvent requirements, and even isotopic labeling—can be manufactured, because we control the whole process. Scale, traceability, and documentation don’t just show up in a glossy brochure—they arrive in every drum and bottle leaving our warehouse.

    The demands on chemical manufacturers continue to grow. Markets require faster turnaround, lower waste, and ever-higher purity. By owning the valerophenone supply process, we keep up with these expectations. This attitude—honest, steady, and technically grounded—reflects everything we learned at the synthesis bench and continue to practice on the production floor.

    Summary

    Valerophenone finds its place as a reliable workhorse in synthetic chemistry, analytical testing, and specialty manufacturing. Years of hands-on manufacturing give us the insight and responsibility to deliver product that matches its reputation. Trust comes from transparency, operational experience, and adaptability—all qualities we bring to every shipment. Whether a project needs a few liters for bench testing or a full container load for industrial scale, valerophenone represents a connection between enduring chemistry and ongoing innovation.