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2-Acetylbenzenecarbonitrile

    • Product Name 2-Acetylbenzenecarbonitrile
    • Einecs 249-876-0
    • 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

    890180

    Chemical Name 2-Acetylbenzenecarbonitrile
    Synonyms 2-Cyanoacetophenone
    Molecular Formula C9H7NO
    Molecular Weight 145.16 g/mol
    Cas Number 4535-23-7
    Appearance White to off-white crystalline solid
    Melting Point 74-77°C
    Boiling Point 312°C
    Density 1.17 g/cm³
    Solubility In Water Slightly soluble
    Smiles CC(=O)C1=CC=CC=C1C#N
    Inchi InChI=1S/C9H7NO/c1-7(11)8-4-2-3-5-9(8)6-10
    Flash Point 142°C
    Storage Conditions Store in a cool, dry, well-ventilated place
    Refractive Index 1.566

    As an accredited 2-Acetylbenzenecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 2-Acetylbenzenecarbonitrile is supplied in a sealed amber glass container with a secure screw cap.
    Shipping 2-Acetylbenzenecarbonitrile is shipped in tightly sealed containers, protected from light and moisture. Transport must comply with local and international regulations for hazardous chemicals. Use appropriate labeling and packaging to prevent leaks or spills. Handle with care, and store in a cool, dry, well-ventilated area during transit to ensure safety.
    Storage 2-Acetylbenzenecarbonitrile should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, segregated from strong oxidizers and acids. Ensure proper chemical labeling and use secondary containment to prevent leaks or spills. Store at room temperature unless otherwise specified by manufacturer guidelines.
    Application of 2-Acetylbenzenecarbonitrile

    Applications of 2-Acetylbenzenecarbonitrile in Industrial Manufacturing

    2-Acetylbenzenecarbonitrile is a key intermediate for multiple value chains in advanced materials and fine chemical synthesis. Our production expertise ensures high batch consistency, which directly supports stringent downstream manufacturing demands. The following applications reflect our customers’ main technical uses across global industrial sectors.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound acts as a critical starting material in the synthesis of complex pharmaceutical intermediates, notably in the production of specific APIs involving benzyl and aromatic nitrile groups. Process chemists favor it for implementing multi-step organic transformations where high purity and conversion rate are necessary, especially in API segments for anti-inflammatory and anticancer drug synthesis. Reaction control relies on precise stoichiometry and defined impurity profiles to meet ICH Q7A requirements. Operators integrate this intermediate at early or middle synthesis stages, where structural modifications and subsequent functional group reactions take place before final API crystallization and purification steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs (if used in US-regulated markets)
    • EDQM CEP certificate for European operations
    • Current Good Manufacturing Practice (CGMP, FDA 21 CFR Parts 210/211)

    Typical usage ratio

    • Used in 0.5–5 molar equivalents relative to target molecule; exact ratio adjusted based on pathway yield and downstream impurity control

    Downstream process integration

    • Charged at synthetic early-stage or intermediate transformation reactors
    • Undergoes nitrile reduction, hydrolysis, or substitution depending on API structure
    • Feeds into continuous or batch synthesis lines prior to final purification and formulation
    • Subject to in-process QC for residual solvents and related substances

    Final product types

    • Benzamide-based active pharmaceutical ingredients
    • Pharmaceutical intermediates for oncology sectors
    • Anti-inflammatory drug pre-intermediates
    • Specialty pharma fine chemicals for CDMO supply

    2. Agrochemical Intermediate Production

    Chemical plants utilize this raw material to build complex molecular scaffolds in the synthesis of key agrochemical actives. Its aromatic nitrile structure serves as a building block for broadleaf herbicides and certain insecticides, where it enters the process before cyclization or ring closure reactions. Manufacturers rely on stringent environmental and occupational health controls for its processing, due to its reactivity and specific impurity profile impact on downstream pesticide registrations. The intermediate is especially valued for its reactivity in chlorination or methylation pathways which enhance the biological activity of final crop protection compounds.

    Industry compliance standards

    • FAO/WHO Guidelines for Quality Control of Pesticides
    • REACH Registration (EU Regulation EC No. 1907/2006)
    • EPA 40 CFR Pesticide Registration
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Primary intermediate: 10–25% of total reaction mass, with ratio dependent on target agrochemical and synthetic yield objectives

    Downstream process integration

    • Added to main reaction vessel after pre-activation of precursors
    • Engages in condensation or cyclization before formulation step
    • Processed under strict temperature and inert atmosphere control
    • Monitored for unreacted content to meet technical material standards

    Final product types

    • Herbicides with substituted benzamide structures
    • Insecticide intermediates containing aromatic nitrile motifs
    • Fungicidal active ingredients precursors
    • Chemical intermediates for custom agro solutions

    3. Liquid Crystal Display (LCD) Material Synthesis

    In the specialty electronics sector, our material serves as a vital intermediate in the synthesis of liquid crystal compounds. Its rigid aromatic structure enables tailorable mesogenic units required in advanced nematic and smectic phase mixtures for high-contrast and wide-viewing displays. Process engineers control its reaction with haloalkyl compounds at precise stoichiometric ratios to optimize alignment layer functionality. Both raw material purity and trace-metal control are tightly managed to avoid downstream electronic performance failures. The compound's integration occurs at targeted steps for pre-polymer or additive formulation stages before large-scale LCD cell assembly.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU) for hazardous substances
    • IEC 61249-2-21 for halogen-free electronic materials
    • ISO 14001 Environmental Management in chemical electronics
    • JIS C5016/JIS C60068 reliability for display segment

    Typical usage ratio

    • 5–15% by weight in base mesogen mixture, tailored based on electro-optical parameter requirements and final product grade

    Downstream process integration

    • Introduced at initial organic synthesis for custom mesogen preparation
    • Further functionalized with halogen or alkyl chains
    • Purified via distillation before blending into final LC mixture
    • Quality confirmed by HPLC and GC for electronics grade certification

    Final product types

    • Mesogenic compounds for TFT-LCDs
    • Organic additives for OLED and LCoS displays
    • Specialty liquid crystal blends for mobile screens
    • High-performance display stabilizers

    4. Fragrance and Flavor Ingredient Precursor

    This product enables the production of fine aromatic aldehydes and ketones for fragrance and flavor synthesis, leveraging its aromatic ketone and nitrile functional groups. Industrial chemists employ reductive or oxidative cleavage to derive unique aroma compounds, which serve as core notes or modifiers in perfumery and food-grade applications. The reaction paths must conform to food and fragrance industry’s allergen and residual solvent regulations, where trace purity and batch reproducibility are critical. Extensive GC-MS analyses are conducted to qualify sub-ppm impurity limits before further formulation in compounded flavor/fragrance bases.

    Industry compliance standards

    • IFRA Standards (for allergen and purity conformity in perfumery)
    • FEMA GRAS (Flavor and Extract Manufacturers Association, food flavorings)
    • 21 CFR 172.515 (FDA GRAS listed synthetic flavoring agents)
    • ISO 9001:2015 with industry-specific HACCP protocols

    Typical usage ratio

    • 0.1–2% in aroma base solution; ratio adjusted based on note intensity, aldehyde conversion efficiency, and regulatory threshold levels

    Downstream process integration

    • Charged into batch reactors during stepwise synthesis of fragrance aldehydes
    • Undergoes controlled hydrogenation or oxidation steps
    • Subject to solvent stripping and headspace GC analysis for trace impurities
    • Final isolates blended into creation or food-grade fragrance oil

    Final product types

    • Synthetic fragrant aldehydes for fine perfumery
    • Ketone intermediates used in flavor compounds
    • Aromatic modifiers for household and personal care fragrances
    • Flavor intermediates for beverage applications
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    Certification & Compliance
    More Introduction

    2-Acetylbenzenecarbonitrile: Proven Quality from a Chemical Manufacturer's Perspective

    Overview of 2-Acetylbenzenecarbonitrile

    From years of hands-on experience in chemical synthesis, I can say that 2-Acetylbenzenecarbonitrile, also called o-acetylbenzonitrile, brings reliability and strong performance in fields like pharmaceuticals, agrochemical intermediates, and specialty chemical manufacturing. The molecular formula C9H7NO and a CAS number of 613-88-7 outline a structure that combines a benzene ring, a nitrile, and an acetyl group in the ortho position, giving it reactivity that is well understood in the lab.

    Our production lines maintain strict consistency batch to batch, prioritizing not only the published purity, but the subtleties within each run that show up in downstream processes. Standard QC includes GC and HPLC analyses. Our material achieves assay values above 99%, and we keep water content and volatile impurities well below established thresholds to prevent any issues during coupling or condensation reactions. Having worked with a wide range of heterocyclic and aromatic intermediates, it’s clear that trace side-products—chalcones, phthalimides, polycyclic contaminants—can cause chaos in scale-up or crystallization stages. In our own work, systematic equipment cleaning and solvent selection directly impact the color and solubility of the product, and we never take shortcuts here.

    Physical and Chemical Character

    Under room temperature, 2-Acetylbenzenecarbonitrile appears as an off-white to pale yellow crystalline solid. With a melting point near 41-45°C and a boiling point higher than many simple nitriles (around 155-160°C at reduced pressure), you need practical knowledge about thermal handling and storage. We’ve optimized packaging into sealed, inert atmosphere containers about two decades ago, after discovering that small traces of moisture or oxygen can prompt slow oxidation, affecting both the appearance and assay. No credible chemical manufacturer can overlook the relationship between the physical state of an intermediate and its behavior downstream. 2-Acetylbenzenecarbonitrile dissolves in common organic solvents—ether, acetone, dichloromethane—at predictable loadings, which helps whether you’re running preparative chromatography or pipelining into a Grignard formation.

    Unlike many simpler aromatics, this compound carries both electron-withdrawing (nitrile) and electron-donating (acetyl) character on adjacent positions. That arrangement influences not just the reactivity but the odor and stability. We’re careful about not over-chilling or heating during filtration and drying, because lessons learned from past incidents have shown that abrupt temperature changes can alter crystal habit, making downstream drying or milling more difficult.

    Strength of Use in Pharmaceutical and Agrochemical Sectors

    Most people ask about the real-world value of 2-Acetylbenzenecarbonitrile inside a synthetic route. In pharmaceutical research, this intermediate contributes to the synthesis of several APIs, notably in pathways involving isoquinolines, substituted quinolines, or benzamide structures. Aromatic nitriles like this serve as building blocks for benzodiazepine cores, anti-hypertensive agents, or anti-cancer drug leads. You soon see that standardization matters: inconsistent input from a supplier leads to failure in hydrogenation, metalation, or condensation stages, forcing unwanted delays and unnecessary cost.

    For pesticide and herbicide R&D, our 2-Acetylbenzenecarbonitrile forms reactive intermediates used to make pyridine derivatives, which in turn push into pyrazoles, triazoles, or phenoxy functions. Yield and conversion depend on not just the purity, but the impurity profile—particular trace acids or bases can derail finely-tuned catalyst systems. We work with plant and process engineers to adjust process parameters, always sharing actual production runs and analytical spectra rather than theoretical statements.

    Comparison to Related Aromatic Nitriles

    Having handled a broad spectrum of aromatic nitriles, I can tell you: not all nitrile intermediates behave the same, even at comparable purity. Take benzonitrile or 4-acetylbenzonitrile as examples. Benzonitrile lacks the ortho-acetyl group and exhibits much lower reactivity during enolate formation or Friedel-Crafts acylation. On the other hand, 4-acetylbenzonitrile positions the ketone at the para position, which means electronic effects don’t enhance neighboring group participation in nucleophilic substitution quite as effectively. Our own field trials show clear differences in both yields and workup complexity, depending on where each functional group lands.

    In terms of solubility and handling, 2-Acetylbenzenecarbonitrile can be separated from homologous compounds easily during column chromatography—its polar character gives sharper elution profiles, especially on silica gel. We sometimes see clients using mixed aromatic nitriles only to discover awkward co-elution problems, which then bleed into spectral impurity downstream. Our feedback loops often involve real chromatograms and UV-Vis spectra, since real-life recovery yields do not always track purity on paper.

    Reliable and Safe Production Practices

    Consistency in the chemical industry hinges on getting the upstream parameters right. Bringing up a batch of 2-Acetylbenzenecarbonitrile in a stirred tank reactor looks straightforward, but only extensive trial runs and careful scaling will prevent fouling, color development, or loss of volatile organics. Early on, we relied on traditional acid-catalyzed acylation routes, but later switched to milder Friedel–Crafts conditions to cut down on byproduct buildup. Waste handling stepped up as we fine-tuned reaction workups with less hydrochloric acid or sulfuric acid footprint.

    Storage is another major concern. As a practitioner, seeing the impact of light and atmospheric moisture on sensitive aromatics leaves a lasting impression. We schedule shipment packing late in the workflow, right after nitrogen-purged, double-sealed containers get closed. This extra step raises shelf life and, more importantly, ensures less drift in quality certificates over time. Many newer entrants overlook these details, only to realize too late that stability claims don’t hold up after export to regions with variable climate conditions.

    Analytical and Quality Control Approaches

    Routine identity checks start with proton and carbon NMR; we look for the signature chemical shifts around 2.6 ppm (acetyl methyl) and downfield aromatic and nitrile peaks. Every produced batch undergoes mass spectrometry to verify molecular weight, and IR spectra should show the sharp nitrile stretch near 2230 cm–1 beside the carbonyl peaks. GC retention is often compared to certified standards from our previous batches, enabling us to spot subtle changes before the product heads into shipping.

    Internal standards, consistent sample prep, and calibration blanks form the backbone of our QC routines. Our QC team tracks every deviation, cross-checking against historical data gathered over many thousands of kilograms’ worth of production. Pattern recognition—like a sudden uptick in a low-level impurity—signals either a raw material or process drift, and we communicate this internally before the market ever hears about it. Failures are logged and process adjustments follow; no reputable manufacturer looks at quality control as a single checkpoint or paperwork step.

    For customers scaling from research batch to ton-scale syntheses, open sharing of method details and impurity profiles makes a difference to process chemists struggling to replicate lab results at scale. We design our certificates of analysis and batch records with this end-use in mind, giving application development teams more data than what shows up on a typical datasheet.

    Downstream Preparation and Isolation: Common Pitfalls and Best Practices

    In our experience, handling after synthesis is as critical as purity itself. Over the years, we’ve seen clients underappreciate the role of controlled crystallization—especially if they move to rapid solvent evaporation or vacuum drying under non-ideal pressures. If the product forms large, fused masses, downstream milling becomes a headache. On the other hand, too rapid chilling produces clumpy powders or oily films, which complicate both transfer and long-term storage. We use a staggered cooling profile and staged solvent removal, refining procedures every few years as better insights arise from actual plant feedback.

    We avoid storing 2-Acetylbenzenecarbonitrile in open bins, recognizing from past incidents that even minor solvent vapor in storage rooms can result in material sticking or caking by the time it's repacked or sampled for analysis. Incremental improvements—like nitrogen-flushed blenders and smaller drum sizes for export—came from listening to what really happens in users’ labs and warehouses, not just from reviewing the old literature.

    If customers blend 2-Acetylbenzenecarbonitrile with strong bases or oxidizing reagents, we advise precise stoichiometry and slow addition, based on thermal analysis of reactivity. This input doesn’t just come from published reaction tables; it arises from direct experience with runaway cases and cold batch failures in actual plant settings.

    Why Specification Rigor Matters in a Crowded Market

    With demand for specialized benzene derivatives rising, especially in regulated industries, the temptation grows for some suppliers to chase specs at the expense of practical quality. As people who have seen both smooth scale-ups and painful recalls, we know that narrow specs like “≥99% purity” only tell part of the story. Leftover isomers or solvents, trace iron or alkali metals—these remain invisible to casual testing but play havoc in exacting multi-step syntheses. Internally, every process revision starts with a root-cause review of failed batches, not just a focus on what went right. You can spot the difference between solid, reproducible manufacturing and “hit-or-miss” supply within a few batches.

    Because regulatory environments keep evolving, especially regarding aromatic intermediates, accountability comes front and center. We maintain full traceability for each lot, not just because auditors ask for it, but because years of observing product recalls and analytical failures across different markets have convinced us it is the only way to build real trust. Being upfront with stability data, impurity tracking, and deviation records turns out to be less hassle in the long run than having to field complaints and dig through incomplete old records.

    Environmental and Safety Considerations from a Production Standpoint

    Active efforts at reducing environmental impact grew out of direct observations of solvent waste generation during early syntheses. Our methods now emphasize solvent recovery and minimal water generation. Insisting on lower-energy thermal profiles and improved filtration cut total energy use significantly, and periodic in-house reviews aim to identify stray emissions even if they remain below regulated limits. In actual operation, these environmental adjustments intersect with personnel safety—nitrile intermediates like this one can provoke skin or mucosa irritation, so we run continuous PPE training and enforce local exhaust protocols in every work zone.

    We also engage with downstream users on safe storage and shipping practices, stressing the need for well-sealed containers, dry environment storage, and restricted access to handling zones. Our own accident logs show that nearly all near-misses involved either storage lapses or rushed loading operations, reinforcing the need for slow, methodical packing and inventory management, not just central process controls.

    By sharing these insights with clients—across pharmaceuticals, agrichemicals, and flavor/fragrance intermediates—we reinforce that environmental and safety credibility depends not on slogans, but on day-to-day vigilance.

    Expertise: The Value of Decades in Direct Manufacturing

    The difference between a serious chemical producer and a middleman lies in how many corners get cut for short-term savings. Tools like automated titration, in-line spectrometric process analytics, and remote temperature/humidity monitoring all mean little if the operation lacks a culture of ownership—from raw material intake all the way to final drum closure. Several times each year, we revisit every raw material and utility vendor, pushing for continuous improvement in both cost control and reliability. Small reductions in solvent residue, faster batch cooling, or improved filtration speed always translate into better material for the chemist at the bench and the engineer at the plant. And we maintain open channels with both, leveraging shared troubleshooting data to make every batch improvement sustainable.

    As more downstream systems require validation and traceability, sharing not just compliance certificates but complete process logs, spectral libraries, and deviation records becomes second nature to us. Our technical team keeps engagement open with development chemists or engineers at each customer site, applying decades of know-how to make sure materials behave the way they are needed in real world, scaled-up conditions—not just in the test tube. This feedback loop has driven nearly all meaningful improvements to our grades of 2-Acetylbenzenecarbonitrile—whether in reducing dust, streamlining handling, or minimizing seasonal drift in quality.

    Troubleshooting Challenges Together

    Real-world manufacturing rarely follows the expected textbook script. Customers often approach us needing to solve tough problems—unexpected color changes, variegated melting points, or complex impurity build-ups during their specific syntheses. Drawing on years of line experience, we tackle issues cooperatively, sending out new lots for trial, or recommending in-process tweaks for milling, drying, or feed addition. A key lesson learned is simple: long-term reliability never comes from simply hitting an assay target or filling out a checklist. It depends on the continual feedback loop between the manufacturer and the people actually using the material in their specific context.

    Our crisis logs have shown repeatedly that early, honest data sharing—about an off-batch or even a missed impurity spec—prevents nearly all escalation. It builds joint problem-solving capacity, addresses problems while they’re still small, and cements working relationships. Over time, this grows into genuine risk minimization for everyone in the value chain, yielding fewer supply interruptions and unexpected failures.

    Looking Forward: The Evolving Role of 2-Acetylbenzenecarbonitrile

    Markets shift: as new synthetic methods develop and as regulatory windows change, the precise formulation and supply of intermediates like 2-Acetylbenzenecarbonitrile will keep moving. Our current lines are already reviewing catalytic upgrades and working closely with advanced users on next-gen precursors. Raw material sourcing remains a challenge, as volatility in the benzene derivatives market has created sporadic supply-side hurdles. We counter this with multi-source procurement, contract storage, and close risk screening of all suppliers. This approach is expensive, but in direct manufacturing, the real cost hits when a customer line goes down or a new impurity sneaks into a critical batch.

    As new research explores even more advanced aromatic substitutions—especially in fields like OLEDs, battery chemicals, or medicinal agents—scale-up demands sharper specs and steadier batch profiles. Our aim is to be ahead of technical problems before they impact either our customers or our own teams. That starts and ends with real knowledge, field data, and unfiltered process awareness—not slick marketing or buzzwords.

    Final Thoughts from Everyday Practice

    To us, 2-Acetylbenzenecarbonitrile is not a faceless catalogue entry or a generic lab chemical. It’s the product of years of tuning, learning from failed batches and rejected lots, directly engaging with engineers and chemists, and paying attention to the practical requirements at both the bench and the plant scale. Our reputation and that of our clients run together, batch for batch.

    Every drum of this intermediate that leaves our plant reflects a chain of practical decisions and careful oversight. We see each customer not as an order number, but as a serious partner in an ongoing technical journey, where steady improvement, transparent feedback, and hard-earned reliability always trump packaging and slogans. We stand by the value that comes from direct experience, detailed record-keeping, and honest engagement, ensuring that every lot of 2-Acetylbenzenecarbonitrile pulled from our line performs to the expectations of professionals who know first-hand what real-world chemistry demands.