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HS Code |
208429 |
| Cas Number | 13361-32-5 |
| Molecular Formula | C9H7NO |
| Molecular Weight | 145.16 |
| Iupac Name | 3-acetylbenzonitrile |
| Appearance | White to off-white solid |
| Melting Point | 54-57°C |
| Boiling Point | 312°C |
| Density | 1.13 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | CC(=O)c1cccc(C#N)c1 |
As an accredited 3-Acetylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle securely sealed, labeled "3-Acetylbenzonitrile," featuring hazard symbols and detailed chemical information. |
| Shipping | 3-Acetylbenzonitrile is shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a solid or liquid, labeled with appropriate hazard warnings. The package complies with chemical transport regulations, and storage conditions during shipping are monitored to avoid exposure to heat, direct sunlight, and incompatible substances. |
| Storage | 3-Acetylbenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Proper chemical labeling is essential, and access should be restricted to trained personnel. Store according to institutional and regulatory safety guidelines. |
Applications of 3-Acetylbenzonitrile in Industrial Manufacturing3-Acetylbenzonitrile provides targeted functionality and molecular reactivity in advanced chemical synthesis routes. As an established intermediate, it supports core innovation across multiple specialized manufacturing sectors. Below, our application overview details actual industry uses, handling requirements, integration points, and related compliance frameworks. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis compound serves as a critical building block in producing various APIs, particularly for CNS agents and anticancer compounds. API manufacturers use it in multi-step synthesis when introducing functionalized aromatic moieties is necessary. 3-Acetylbenzonitrile participates in Friedel–Crafts acylation and further transforms under controlled conditions, where its purity and trace impurity profile directly influence the final product’s regulatory acceptability. Industry compliance standards
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2. Advanced Agrochemical Synthesis (Herbicide Intermediates)Producers utilize 3-Acetylbenzonitrile for the synthesis of substituted benzamide structures featured in new-generation pre-emergent herbicides. Its electronic and steric characteristics support the construction of target molecules through amide coupling, delivering key functional groups recognized in agrochemical performance claims. Downstream firms demand consistent nitrile content and precise impurity control to meet agricultural registration standards. Industry compliance standards
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3. Specialty Dye and Pigment IntermediateDye manufacturers incorporate this compound for synthesizing high-performance anthraquinone derivatives and azo intermediates. Its role is central in condensation or acylation steps that introduce nitrogen functionalities for chromophore elaboration. Quality protocols require precise control of color index values and heavy metal absences, directly affecting finished pigment dispersibility and shade uniformity. Industry compliance standards
Typical usage ratio
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4. Synthesis of Electronic and Photonic MaterialsProducers of specialty electronic chemicals use this compound for manufacturing liquid crystal intermediates and other aromatic nitrile derivatives needed in high-performance display and sensor applications. Its cyano and acetyl groups permit functional flexibility in assembling molecules for fine patterning, stability, and band-gap tailoring. Process integrity and electronic purity standards govern the selection and qualification for use in these sensitive sectors. Industry compliance standards
Typical usage ratio
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Manufacturing 3-acetylbenzonitrile over the years has shown us how much value precise chemistry brings to technical fields. We have watched this compound serve research, pharmaceutical synthesis, and specialty chemical development. Reactions and formulations that need a reliable building block keep turning to 3-acetylbenzonitrile—its presence in our factory’s operations comes from consistent demand backed by its performance on the molecular level.
Our process relies on years of careful optimization. The main product, 3-acetylbenzonitrile, carries the chemical formula C9H7NO and a molecular weight of 145.16. The off-white to pale yellow crystalline appearance has come to represent a well-made batch in our packaging hall. We keep water content under 0.5%, and work to maintain purity between 98% and 99.5%, based on titration and chromatography. By managing raw material sources and performing in-process controls, the risk of unexpected impurities stays low—another key to stable output.
Over time, we have pushed to improve reproducibility. Consistency wins trust in the synthetic organic chemistry space, and we have put our process through enough scale-ups (from pilot reactor runs up to commercial tonnage) to understand where batch anomalies can start. Each time we process precursors and carry out Friedel–Crafts acylation followed by dehydration and aromatic nitrile isolation, we focus on solvent control, temperature profile, and crystallization rate. Even slight variations in agitation or filtration lead to changes in optical clarity and melting point—details visible only to people who watch the product day after day. Feedback from chemists using our samples in HPLC and NMR work has pushed us to tighten particle size distribution, as larger crystals raise concerns with solubility and dose reproducibility.
For synthetic organic chemists, 3-acetylbenzonitrile gives access to a range of functional transformations that less robust benzonitrile derivatives do not. It offers the versatility to serve as a precursor in pharmaceutical intermediates, especially for molecules with aromatic rings bearing both nitrile and carbonyl functional groups. This dual reactivity opens several reaction pathways—condensations, reductions, or cyclizations can all start from a single bottle. The acetyl group at the meta position means regioselectivity for substitution is more predictable, allowing for stepwise synthesis targeting advanced intermediates and final actives.
In-house, our facility handles requests for both R&D and kilogram-scale batches. Some clients develop building blocks for anti-inflammatory drugs or CNS agents, where the position of the acetyl and nitrile groups in the ring affects bioactivity and downstream derivatization. We have seen demand rise in custom peptide and heterocycle assembly, as chemists seek handles for palladium-catalyzed couplings or nucleophilic aromatic substitutions. Unlike less functionalized benzonitriles, the acetyl group at position 3 imparts steric and electronic effects that can be exploited in more complex molecule design.
Each use case brings different requirements for purity. Some process chemists run multi-step syntheses that amplify any impurity, so we work with their teams to ensure custom specifications. Our analytical staff adjusts HPLC gradients and looks for minor byproducts—a benefit only experienced hands can provide, especially where scale-up exposes hidden issues. Over time, these close collaborations teach both us and our partners what matters, creating feedback loops that fine-tune every delivery.
Several factors distinguish our 3-acetylbenzonitrile from simpler benzonitriles or alternative isomers. Substitution pattern on the aromatic ring directly impacts both chemical reactivity and downstream applications. The 3-acetyl isomer avoids ortho effects that trouble some syntheses, offering cleaner routes to derivatives where the acetyl and nitrile functions act independently. Compared to 2- or 4-acetylbenzonitrile, the meta orientation can suppress side reactions—this traits appeals to chemists aiming for straightforward protection or deprotection, or clean cross-coupling at remote positions.
We keep up with feedback comparing our batches to those from other manufacturers. Purity alone does not tell the whole story; ease of handling and solubility must also deliver. Our own reaction development group regularly tests product lots in downstream functionalizations—Grignard additions, Suzuki-Miyaura cross-coupling, hydrogenations—to ensure expected yields without strange byproducts. Starting with poorly controlled material introduces hesitancy when researchers scale up; trust grows with experience and reproducibility.
It is easy to overlook how even trace variation in isomeric content or residual solvents affects analytical outcomes. Mass spectrometry or NMR assignments can blur when contaminants linger. We use GC-MS and FT-IR to check for trace aromatic byproducts and residual process solvents. Combined with customer feedback and internal usage data, these controls have rewarded us with fewer repeat quality queries and more confidence during in-house scale-up projects. Having a dedicated laboratory for analytical follow-up means patterns are caught before they escalate into formal complaints or, worse, failed production campaigns.
Scaling any aromatic cyanation process brings unique challenges. The hazards of handling nitrile precursors demand discipline in atmospheric controls and wastewater management. Early in our operation, we dealt with off-gassing during dehydration steps, learning through trial, error, and external audit. Adjusting vacuum and distillation rates, and redesigning scrubber systems, were hard-won upgrades. Teams familiar with these practicalities carry that experience into each new batch, consulting both new process engineers and neighboring departments on handling unexpected results.
We have seen how trace water introduces hydrolysis risk in the acetyl group, causing unwanted ring opening or hydroxyacetophenone formation. This explained a few off-spec lots encountered during humid months, leading us to revise dehumidification in packing rooms. Those lessons have paid off by keeping our off-site clients confident in shipment stability. Effective moisture exclusion makes the difference between a material that succeeds in precise organic syntheses versus one repeatedly flagged for instability or low conversion.
Machine maintenance and operator training have become central themes. A single misstep in temperature ramp or solvent recycling meant lost batches and unnecessary waste. Continuous education on cleaning protocols prevents cross-contamination, especially during high-volume runs of related aromatic nitriles. Integration of process analytical technology has given operators better visibility—feedback loops from inline solvent detectors or temperature probes help catch deviations before they cascade through a production campaign.
Process safety matters. Cyanide-based chemistry requires strict ventilation and emergency responses. Our internal procedures went through revision after close calls in early years. Partnering with local authorities for emergency drills, and investing in operator certification, keeps both our staff and the community confident in our control methods. These are non-negotiable aspects of responsible manufacturing practice, reinforced in every batch record and shift handover.
Technical support has become inseparable from our offering. Research partners often need alternative batch sizes, analytical data packages, or parallel samples for comparison. Our in-house research chemists answer application questions and provide literature support—real communication, not off-the-shelf responses. When a customer wanted to know about trace impurity formation during purification, our team tested distillation at various reflux ratios and supplied chromatographic data for risk assessment; that turned out to save a six-week investigation at their site.
As new discovery programs pick up, we keep up with demand by adjusting batch planning and ship dates. We have learned to keep a small stock of high-purity lots ready, especially for contracts involving time-sensitive clinical trial development. That allows us to handle urgent orders, minimize wait times, and work with partners as timelines shift. Providing reproducibility between batches proves essential in analytical method validation work—this builds confidence for those transitioning from laboratory to pilot scale.
We keep ahead on regulatory and documentation needs. Customer site audits and requests for detailed impurity profiles make full documentation essential. Our team keeps batch-by-batch certificates, spectral archives, and impurity trend reports. These are not just paper exercises—they support real decision-making at customer R&D meetings and during technology transfers. Feedback leads us to adjust both specification targets and data presentation methods, improving transparency and resolving clarification requests before they escalate.
Over the last decade, reliability of raw material sourcing has required close, ongoing relationships with upstream suppliers. We often visit upstream plants and cross-validate supplier certificates with our own incoming QC. Early in our history we learned that accepting third-party representations without verification invited variation and occasionally counterfeit product. Direct connection with those producing the starting benzene derivatives and catalyst materials has made a tangible difference in our ability to promise both volume and quality.
Raw material authenticity does not only impact regulatory compliance. Impurities introduced at early stages become amplified downstream, especially as process steps build on one another. We saw one incident where unidentified aromatic contamination forced a recall and full audit of a supply relationship. Since then, supplier management includes material traceability, regular site visits, and fallback contracts on two continents. This discipline saves cost and effort over endless troubleshooting.
Market swings happen, especially with volatility in global chemical feedstocks. By keeping buffer stocks and developing alternative supply routes, we weather short-term price spikes and unexpected shortages. Parallel qualification of backup material sources—without diluting quality expectations—keeps our process stable during raw material unavailability. Only long-term planning and investment in strategic storage allow this level of stability for customers who need reassurance on delivery timelines.
Variation in batches, especially across manufacturers, usually comes down to sources of starting materials, operator discipline, and attention to small details like drying and mother liquor disposal. Some makers chase price by cutting corners on purification, which frequently introduces low-level aromatic or carbonyl-containing byproducts. We have received samples of competitor material with visible yellow tint, signaling either residual catalyst or incomplete washing. Our approach has always prioritized control over every stage—from raw material test, through reaction, to packaging and shipment.
Clients sometimes question price differences across suppliers. The answer nearly always lies in subtle but critical distinctions: a higher-purity batch avoids headaches in late-stage synthesis and reduces waste from purification processes at the customer’s site. It is a small upfront expense for downstream reliability; something we document by compiling customer feedback and in-process analytical monitoring. A record of delivering as promised brings repeat business, even when alternative suppliers quote lower prices.
Working with university labs and industrial pilot plants also opens our eyes to real-world challenges: minor differences in melting point, color, or solubility can mean hours of lost productivity for research chemists or process engineers. Delivering product that behaves predictably from the first test batch through process qualification saves time, supports publications, and lowers cost in scale-up. Our consistent batches remain a point of pride for our manufacturing and QC teams—feedback that a given batch “just works” in downstream syntheses matters more to us than volume sold.
Making 3-acetylbenzonitrile to consistent internal standards motivates us to keep learning. Collaboration with research partners, industrial clients, and regulatory authorities keeps our teams sharp. We keep up with new reaction methodologies published in the literature, adapting process controls to better match future needs. Our technical support team monitors new downstream synthesis techniques, advising on likely fit and challenges so that both parties avoid dead-ends and unnecessary waste. Participation in conferences and technical workshops keeps the flow of information alive, building connections for mutual learning.
Continuous improvement often springs from feedback. We revise specifications and change handling practices as research advances. Working together, both manufacturer and end user push each other to higher standards. Occasionally, a seemingly small detail in packaging or documentation reveals an improvement opportunity. These cumulative changes raise overall product reliability—ten separate incremental upgrades over a year represent major change in the confidence downstream users can place in our material. They also ensure every process step, from synthesis to shipment, reflects both current and future client expectations.
Our goal centers on long-term trust. New technology, better analytics, and closer partnerships form the backbone of that trust. In producing 3-acetylbenzonitrile, we recognize that everything starts with people: skilled chemists, detail-focused operators, and responsive technical support. We stay accountable to those using our product, confident that our daily attention to each detail—batch after batch—brings value well beyond the chemical formula.