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HS Code |
806128 |
| Chemical Name | O-Chlorobenzonitrile |
| Synonyms | 2-Chlorobenzonitrile |
| Cas Number | 873-32-5 |
| Molecular Formula | C7H4ClN |
| Molecular Weight | 137.57 g/mol |
| Appearance | White to pale yellow crystalline solid |
| Melting Point | 35-38 °C |
| Boiling Point | 220-222 °C |
| Density | 1.23 g/cm³ at 25 °C |
| Solubility In Water | Slightly soluble |
| Flash Point | 105 °C (closed cup) |
| Odor | Aromatic odor |
As an accredited O-Chlorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of O-Chlorobenzonitrile is packed in a sealed amber glass bottle with a hazard label and secure screw cap. |
| Shipping | O-Chlorobenzonitrile should be shipped in tightly sealed containers, away from heat, sparks, and open flames. It must be labeled as hazardous, with appropriate UN number (UN 3286), and transported according to regulations for toxic and potentially flammable organic chemicals. Wear protective gear when handling and keep away from incompatible substances. |
| Storage | O-Chlorobenzonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store away from sources of ignition and heat. Ensure the storage area is clearly labeled and equipped with spill containment and proper ventilation to minimize exposure and hazards. |
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Purity 99%: O-Chlorobenzonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity active ingredient production. Melting Point 45°C: O-Chlorobenzonitrile with a melting point of 45°C is used in fine chemical formulation, where it enables precise process control and consistent product quality. Stability Temperature 120°C: O-Chlorobenzonitrile with stability temperature of 120°C is used in industrial dye manufacturing, where it provides thermal resistance during high-temperature reactions. Particle Size <50 μm: O-Chlorobenzonitrile with particle size less than 50 μm is used in specialty pigment processing, where it allows uniform dispersion and enhanced coloration properties. Molecular Weight 119.54 g/mol: O-Chlorobenzonitrile with molecular weight 119.54 g/mol is used in agrochemical synthesis, where it contributes to controlled reactivity and target compound specificity. Water Content <0.1%: O-Chlorobenzonitrile with water content below 0.1% is used in electronics material production, where it minimizes hydrolysis risks and improves product stability. Refractive Index 1.525: O-Chlorobenzonitrile with refractive index 1.525 is used in optical resin modification, where it enhances light transmission and end-product clarity. Density 1.18 g/cm³: O-Chlorobenzonitrile with density 1.18 g/cm³ is used in organic synthesis research, where it facilitates accurate volumetric dosing and reproducible reaction outcomes. |
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Many conversations around industrial chemicals can get technical in a hurry, but sometimes it pays to step back and look at how a single compound, like O-Chlorobenzonitrile, fits into real-world production and research. Whether you're working the bench in a synthetic chemistry lab, overseeing plant operations in pharmaceuticals, or navigating procurement in agrochemical manufacturing, O-Chlorobenzonitrile finds its way into more projects than most people realize. Its structure and properties set it apart from other benzonitriles, and its place in both large-scale and small-batch chemistry deserves a spotlight.
O-Chlorobenzonitrile, also recognized under its chemical structure as 2-chlorobenzonitrile, is an organic compound sporting both a cyano group and a chlorine atom attached to a benzene ring. The ‘ortho’ (or ‘O-’) in the name means the chlorine and cyano groups sit next to each other, which, in practice, gives the compound distinctive reactivity compared to its meta and para cousins. This small detail in molecular design shifts its role in synthetic routes and the types of reactions it undergoes.
It's not flashy. O-Chlorobenzonitrile doesn’t arrive with the aura of cutting-edge biotech or the recognition of household cleaning agents, but its simplicity is its selling point. This compound pitches up in everything from pharmaceutical syntheses to dye intermediates, making it a staple tool for chemists and engineers. It serves as both a reactant and a precursor to products layered throughout supply chains in multiple industries.
O-Chlorobenzonitrile typically appears as a white to off-white crystalline powder and carries a sharp, somewhat acrid odor. It boasts a melting point hovering around 42-44°C, and a boiling point near 222°C. High purity batches—often 99 percent or above—form the backbone of pharmaceutical and specialty chemical work, as even trace impurities can complicate downstream reactions.
Most commercially available O-Chlorobenzonitrile balances shelf life and handling safety. Moisture content is monitored closely, and packages usually seal out air and water vapor to avoid degradation. From personal experience in process development, picking a consistent supplier and paying attention to storage conditions pays dividends in both yield and product quality. There’s nothing more frustrating than discovering your main ingredient has picked up water and ruined a sensitive reaction, which can set projects back days or weeks.
At first glance, O-Chlorobenzonitrile may appear like one more benzonitrile variant among many, but its ortho substitution pattern opens doors in several directions:
People sometimes overlook these intermediates because they rarely appear in finished consumer products, but their absence can stall production lines, throw off research timelines, and raise costs downstream. Reliability and predictability count in real-world manufacturing, and O-Chlorobenzonitrile delivers both.
The "ortho" configuration changes more than just the molecular diagram—it's a game-changer in terms of reactivity. Chemists often debate whether to use O-, M-, or P-Chlorobenzonitrile, and those choices shape project outcomes. In the O- version, close proximity between the two groups can drive unique reactions, such as intramolecular cyclizations or nucleophilic aromatic substitutions that wouldn’t be feasible with meta or para substitution.
This increased reactivity can be a blessing or a curse, depending on the desired outcome. I've had moments in the lab where switching from para to ortho led to shorter routes, fewer purification steps, and better yields. Other times, the same reactivity made handling more finicky, requiring tighter temperature control or modified solvents to avoid side products.
On the regulatory side, O-Chlorobenzonitrile doesn’t raise the same red flags as more persistent pollutants. It breaks down more readily than heavier chlorinated aromatics, and safety protocols are easy to follow for experienced operators. Like many niche intermediates, specialized handling is expected, and plant operators who've worked with this compound for years often have their own tricks to minimize exposure and waste.
Like many bulk organic chemicals, the global market for O-Chlorobenzonitrile faces its ups and downs. Fluctuations in raw material prices, changes in environmental regulations, and swings in demand for downstream products create plenty of uncertainty for buyers and sellers. During the pandemic, supply chain snarls caused lead times to double, as both raw material suppliers and shipping firms struggled to keep up.
From my perspective, diversifying sources and supporting domestic production pays off over the long haul. International sourcing may look cheaper on paper, but a supply disruption can quickly erase those savings—and cause headaches for everyone from project chemists to inventory planners. Companies sticking with a single overseas supplier often have longer recovery times if a shipment gets delayed or an export restriction bites.
There’s also a trust factor that’s overlooked in procurement discussions. If your main supplier consistently meets promised purity specs and delivery dates, your research team can run experiments or your plant can operate without scrambling for backup plans. In applications where O-Chlorobenzonitrile functions as a critical path intermediate, confidence in the supply chain frees up more time for innovation rather than firefighting.
Safety handling rules for O-Chlorobenzonitrile don't deviate far from standard practice for related nitriles and chlorinated aromatics—my own habits include good ventilation, nitrile gloves, and care with waste collection. The compound doesn’t linger in the environment like heavily halogenated relatives, which makes waste management less burdensome. Plant EHS (environment, health, and safety) managers I've spoken with appreciate that the pathways for disposal are well understood, and permit approvals usually move quickly when established incineration protocols are in place.
There’s ongoing discussion in the scientific community around greener synthesis routes, seeking to cut down hazardous byproducts and improve overall atom economy. A few process teams in Europe and Asia have rolled out catalytic approaches that trim waste and lower energy usage, but adoption remains spotty outside large multinationals. Everyone wants greener chemistry, but tight margins and the inertia of legacy process equipment slow down widespread change. If regulatory pressure or end-user demand for sustainability increases, O-Chlorobenzonitrile suppliers able to demonstrate cleaner processes and fully disclosed EHS documentation will stand out.
One pattern stands out from years of working in specialty chemicals: the value of deep expertise in handling these compounds. Labs and production facilities that invest in operator training, clear protocols, and robust QA (quality assurance) systems for intermediates like O-Chlorobenzonitrile see fewer accidents and less product loss. New hires often underestimate how subtle differences between ortho, meta, and para isomers alter reactivity, and seasoned staff help avoid expensive mistakes.
For organizations building in-house capacity to manufacture or use O-Chlorobenzonitrile, time spent on education pays off. On more than one occasion, quick thinking by a process tech or lab supervisor has caught a potential quality drift or process upset before it spiraled into a much larger problem. It might sound dry, but repetition, documentation, and structured mentoring create a culture of safety and reliability. This is the real backbone of consistent O-Chlorobenzonitrile application: skilled people who treat the handling of every drum and flask with care.
Chemical research keeps uncovering fresh territory for known intermediates, and O-Chlorobenzonitrile is no exception. Medicinal chemists, in particular, continue to find new ways to leverage the ortho effect to unlock novel bioactive molecules. Whether it’s designing a more potent kinase inhibitor for cancer therapy or an improved herbicide with reduced field persistence, these innovations push the boundaries of what established building blocks can do.
Process development teams have chipped away at old bottlenecks, streamlining steps to improve overall yield and cut waste. There’s a lot of value in shaving a few percent off the cost per kilogram or reducing purification steps before moving to scale. That kind of progress generally comes not from high-profile breakthroughs, but from steady, incremental improvements. Every plant manager’s annual goal includes maximizing asset utilization, and getting more out of a given throughput of O-Chlorobenzonitrile feeds right into those bonuses.
Startups and academic groups occasionally shake up the landscape with lighter, more sustainable reaction conditions, or by swapping traditional solvents for bio-based alternatives. Although these advances often take years to translate from journal articles to the plant floor, they signal that established building blocks like O-Chlorobenzonitrile will keep evolving as industry needs change. With global trends emphasizing both cost and sustainability, compounds that can adapt to cleaner, faster, and safer synthesis will keep their edge in the commodity and specialty markets alike.
Markets in North America, Europe, and Asia each bring their own dynamics to the story of O-Chlorobenzonitrile. While demand has grown in China and India due to expanding pharmaceutical and agrochemical sectors, established producers in Europe often differentiate on quality, documentation, and environmental standards. Working with manufacturers in multiple locations, I've seen the differences up close—waste water standards, packaging, batch tracking, and even the frequency of independent lab audits set apart suppliers who put care into every shipment.
There are also broader forces at play. Rising scrutiny on chlorinated aromatic compounds has spurred some end users to re-examine specifications, and stricter product stewardship in mature markets gets applied not just at the finished product stage, but all the way back to the intermediates. Companies aware of these shifts—who prepare for tighter scrutiny and transparency—tend to win more repeat business. Real-world compliance doesn’t come from reading the rules once and forgetting about them, but from weaving best practice into every drum shipped and every MSDS file updated.
Trade patterns shift with tariffs, anti-dumping regulations, and transportation costs. Logistical headaches aren’t always predictable, and disruptions from extreme weather, labor actions, or port congestion can temporarily knock markets off balance. The strong performers in O-Chlorobenzonitrile supply learn to expect these surprises, building flexibility into contracts and holding safety stock where needed. Product managers who stay in close contact with their suppliers usually spot trends before they become problems, and they act early to keep production running smoothly.
There’s plenty of chemistry to unpack when stacking up O-Chlorobenzonitrile next to meta and para isomers, or against benzene rings with other substituents. The tight orientation between chlorine and the nitrile group makes the ortho isomer more reactive toward nucleophiles and ring-closure reactions. This can fast-track some synthetic steps, especially in heterocycle formation or where proximity effects speed up otherwise sluggish reactions.
Meta- and para-chlorobenzonitrile typically show less electronic interaction between their substituents, which has both pros and cons. When selectivity and milder reactivity are needed, those isomers come into play. Ortho leads when the goal is to drive transformation rapidly or form certain fused ring systems. Years spent in route scouting taught me that the ortho isomer isn't always the fastest or cheapest option, but it solves unique synthetic puzzles that the others can’t touch. The key is not just picking a product from a catalog, but understanding how that choice shapes your process from raw material through to finished goods.
Sourcing and applying O-Chlorobenzonitrile brings plenty of routine, but that doesn’t mean the path is always straightforward. Real-life hiccups—shipment delays, out-of-spec material, equipment breakdowns—crop up more than glossy brochures might suggest. Solutions usually spring not from heroics, but from teams prepared to adapt and plan ahead. Building long-term relationships with suppliers, cross-training staff, and sharing information across functions keep operations resilient. After all, each drum of O-Chlorobenzonitrile on the loading dock represents steps—and missteps—taken by dozens of people.
Opportunities for improvement don’t dry up either. Chemists and engineers able to ask the tough questions—about process safety, regulatory compliance, waste reduction, or greener alternatives—drive enterprises forward. Whether it’s collaborating across departments to cut energy use on a key transformation, swapping to an improved containment system, or designing a new route using O-Chlorobenzonitrile as a springboard, progress often arrives in steady steps rather than headline breakthroughs. These incremental wins add up to safer plants, cheaper manufacturing, and more sustainable products for society at large.
O-Chlorobenzonitrile rarely makes headlines. Yet, behind the scenes, its reliable performance and peculiar reactivity anchor countless endeavors in synthesis, research, and industrial chemistry. From the factory floor to the research bench, the people who know this molecule keep it moving—quietly shaping the medicines, materials, and technologies the world relies on every day.