|
HS Code |
486871 |
| Product Name | 4-Chlorobenzonitrile |
| Chemical Formula | C7H4ClN |
| Molecular Weight | 137.57 g/mol |
| Cas Number | 104-88-1 |
| Purity | ≥99.0% |
| Appearance | White to off-white crystalline powder |
| Melting Point | 82-86 °C |
| Boiling Point | 251 °C |
| Density | 1.24 g/cm³ (at 25 °C) |
| Solubility In Water | Insoluble |
| Smiles | C1=CC(=CC=C1C#N)Cl |
| Inchi | InChI=1S/C7H4ClN/c8-7-3-1-6(5-9)2-4-7/h1-4H |
| Refractive Index | 1.568 (at 20 °C) |
| Flash Point | 112 °C (closed cup) |
| Storage Temperature | Store at room temperature |
As an accredited 4-Chlorobenzonitrile (≥99.0%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 500g 4-Chlorobenzonitrile (≥99.0%) is packaged in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 4-Chlorobenzonitrile (≥99.0%) is shipped in tightly sealed containers, protected from moisture and incompatible substances. Packaging complies with regulations for hazardous chemicals. Standard shipping options include ground or air, with materials labeled for identification and safety. Handling and transport follow all relevant chemical safety and environmental guidelines. |
| Storage | 4-Chlorobenzonitrile (≥99.0%) should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from heat, ignition sources, and direct sunlight. Keep it separated from strong oxidizing agents and acids. Properly label the container, and ensure storage complies with local regulations and chemical compatibility requirements. Use appropriate personal protective equipment when handling. |
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Synthesis Intermediate: 4-Chlorobenzonitrile (≥99.0%) is used in pharmaceutical intermediate synthesis, where high purity ensures reproducible reaction yields. Purity: 4-Chlorobenzonitrile (≥99.0%) is used in agrochemical production, where ≥99.0% purity reduces side-product formation. Melting Point: 4-Chlorobenzonitrile (≥99.0%) is used in organic synthesis, where a defined melting point allows precise reaction temperature control. Stability: 4-Chlorobenzonitrile (≥99.0%) is used in dye manufacturing, where excellent stability enhances batch-to-batch consistency. Solubility: 4-Chlorobenzonitrile (≥99.0%) is used in material science research, where predictable solubility improves formulation accuracy. Molecular Weight: 4-Chlorobenzonitrile (≥99.0%) is used in heterocyclic compound development, where known molecular weight enables accurate stoichiometry calculations. Chlorinated Aromatic: 4-Chlorobenzonitrile (≥99.0%) is used in specialty chemical synthesis, where the chlorinated aromatic ring increases molecular reactivity. Spectral Purity: 4-Chlorobenzonitrile (≥99.0%) is used in NMR studies, where high spectral purity enables unambiguous structural assignment. Reactivity: 4-Chlorobenzonitrile (≥99.0%) is used in nucleophilic substitution reactions, where enhanced reactivity facilitates efficient product formation. Low Moisture Content: 4-Chlorobenzonitrile (≥99.0%) is used in fine chemical synthesis, where low moisture content minimizes unwanted hydrolysis. |
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Laboratory shelves tell their own stories. Some compounds rarely gather dust, owing to their practical value in organic chemistry. 4-Chlorobenzonitrile—known for its sharp purity, with an assay at or above 99%—ranks high among these. For those who spend much of the day beneath a fume hood or over a reaction flask, the utility of a compound stretches beyond its molecular formula. It’s about reliability, yield, and success in moving projects from concept to result.
The model featured here is a crystalline solid, often off-white to pale yellow, which speaks volumes about its purity. Color is more than cosmetic—slight deviations can signal the presence of trace contaminants. During years spent teaching undergraduate lab courses, I noticed that students focused on the advertised purity of a reagent would often save hours down the road, simply by trusting their starting material. That’s no small detail when a day’s work might hinge on a single transformation.
With a melting range that matches literature values closely—usually around 108°C to 110°C—this batch leaves little doubt. Impure compounds rarely offer that clarity, showing a sluggish, broad melting event. Watching a clean crystal melt smoothly in a capillary tube gives a reassurance that few analytical instruments can match at a glance.
A good reagent carves its own path through industry and the lab. Over time, 4-Chlorobenzonitrile found regular use among people working to develop new pharmaceuticals, advanced materials, and a string of agrochemical intermediates. Its major draw comes from the reactivity of both the nitrile group and the chloro position, sitting on opposite sides of a benzene ring. These features open the door to a range of structural transformations, feeding into more elaborate targets.
Some early days in pharmaceutical research quickly made me appreciate the flexibility offered by this compound. Take an aromatic substitution—few products open up as many downstream functionalizations on both the ring and the nitrile as this one. It lays the groundwork for making substituted anilines, benzoic acids, and other staple motifs. Industrial chemists—especially those operating with the relentless clock of process scale-ups—lean on intermediates that don’t throw curveballs, and this compound fits the bill.
In the lab, synthesis of target molecules often begins with building blocks sturdy enough to withstand sometimes-harsh chemistry. This compound takes aggressive conditions—such as those found in Grignard or lithium-halogen exchange strategies—without losing its backbone. Students and technicians alike notice fewer byproducts clogging up their chromatograms, making a tangible impact on throughput and waste reduction.
Fields far beyond pharmaceuticals also value this product. In materials science, for example, researchers use it to construct advanced dyes and custom polymers. Many specialty polymers start from aromatic nitriles, where the balance of reactivity and selectivity sets the foundation for further innovation.
A 99% minimum purity level offers more than just a small bump above lower grades on paper. Anyone who tried to run standard coupling reactions—like a Suzuki or a Buchwald–Hartwig amination—knows low-grade material can turn these robust methods into frustrating exercises in troubleshooting. I recall a project several years ago where swapping out a mid-grade reagent for a high-purity source salvaged weeks of work and brought NMR spectra into line without persistent mystery peaks.
Low-level impurities can catalyze or poison reactions, even when present in small amounts. With regulatory pressure growing and the cost of lost batches rising, the slight extra investment in top purity often repays itself many times over. In applications geared toward biologically active compounds, trace contaminants can echo downstream, complicating purification or even masking true biological activity.
Distinguishing this product from those labelled as “technical grade” or “reagent grade” matters. Technical material sometimes serves industrial-scale functions where purity is secondary to cost. But where precision drives progress—especially in pharmaceutical intermediates, process optimization, and polymer chemistry—a product that consistently hits or exceeds 99% purity builds trust and cuts down on headaches in both discovery and production environments.
Purity isn’t just about immediate lab outcomes. Safety, regulatory compliance, and sustainability also depend on the predictability of the chemicals being handled. The cleaner the input, the fewer the unknowns. Industry standards—set by organizations such as ISO and GMP guidelines—help steer procurement toward high-grade materials for good reason. Contaminants increase risk to health and the environment and can complicate waste handling.
From experience working in both academic and industrial quality control, the difference between reporting a batch as out-of-spec or clearing it for use often comes down to trace levels of unknowns. Simple steps upstream, like sourcing a consistently pure batch of 4-Chlorobenzonitrile, help organizations meet tightening expectations from regulatory bodies while also protecting their people on the ground.
Managing safety data sheets grows much more straightforward when the profile of impurities narrows. Waste management plans can be less complicated when trace side products are predictable or negligible. Environmental health officers and industrial hygienists, in turn, can better assess risk and make informed recommendations.
Structure tells a functional story. The chloro group at the para position increases the versatility of 4-Chlorobenzonitrile relative to its ortho- or meta- counterparts. In practice, para-substitution sets up a range of chemoselective couplings, where position on the aromatic ring determines the pathway. This simple difference amplifies options in heterocycle synthesis and in preparing disubstituted benzenes—crucial for tuning biological or physical properties.
Chemists intent on constructing biphenyl scaffolds look specifically for this para-nitrile due to its lower steric hindrance. Reaction yields benefit, as do downstream functionalizations, because the product avoids the steric congestion that slows meta- and ortho-substituted compounds. Each person in the lab who runs such reactions knows the relief of cleaner mass spectra and more straightforward workups.
Other benzonitriles exist, but not all deliver the same performance in cross-coupling or nucleophilic aromatic substitution. Highly electron-withdrawing or strongly deactivating substituents can dampen reactivity or steer selectivity off course. In contrast, the single chloride at the para position balances reactivity and stability, bolstering use in a broad range of transformations. It’s a case study in how a small change shapes an entire project portfolio.
For procurement teams, choosing a high-purity intermediate can seem like a small decision in the vast lineup of material considerations. Still, the downstream impact on batch consistency, cost avoidance, and process optimization far outweighs the initial price difference. Talking with scale-up teams, stories emerge where variable impurity profiles forced a halt in production or led to batch rejections that ran up six-figure losses. Avoiding this pain means building supply chains around well-characterized, reproducible products that keep surprises off the table.
As the sector pivots toward green chemistry and process sustainability, reducing rework and minimizing purification steps aligns corporate responsibility with profitability. A nearer-to-ideal starting compound shrinks the carbon footprint of a process, thanks to lower solvent consumption and energy usage. The push for more sustainable operations isn’t a trendy add-on anymore, it’s fast becoming the new normal. Here, high-purity intermediates offer a clear advantage.
Work in chemical development underscores another angle: the ability to bring research discoveries to scale. Startups and large manufacturers both face obstacles jumping from the gram-scale proof-of-concept to the ton-scale pilot. Purity fluctuations between lots are a frequent culprit in process failures and lost time. A dependable 99% purity reduces the noise, delivering a more linear path from R&D to market launch.
Process chemists love a reliable intermediate. Anyone working systems where each new step relies on the cleanup from the last knows the cost and frustration that comes with fighting through low-purity material. In discussions with process engineers, the same themes surface: A cleaner input results in a smoother output, fewer surprises, and more predictable downstream chemistry.
4-Chlorobenzonitrile, produced to high standards, lets teams spend more time focusing on core process improvements—catalyst development, solvent swapping, waste minimization—rather than chasing after errant side reactions. Feedback from in-plant operations points to reduced filter clogging, less time fixing analytical anomalies, and smoother handoffs between shifts.
Users in materials chemistry share a similar story. The product’s predictability supports not just the main reaction, but also the performance and safety of advanced materials in real-world applications. In coatings and electronics, the ability to forecast physical properties depends on fine-tuning input materials—a job made easier with fewer surprises from hidden contaminants.
Across research environments, protecting project momentum matters. Having reliable, high-purity building blocks like this one lessens the risk that a crucial late-stage reaction will fail unexpectedly. Many scientists know the frustration of losing weeks to a bad batch of reagents, particularly when working under publication or patent deadlines. By sticking to dependable, well-tested materials, teams stack the odds in their favor.
Large organizations share these priorities—but with added layers. Regulatory filings, customer audits, and product recalls all link directly back to quality assurance. Building projects on a bedrock of trusted intermediates reduces exposure to compliance risks and recalls. Product recalls cost millions and damage reputations; prevention often starts at the molecular level.
In my career, I’ve watched safety and quality managers repeatedly emphasize the role of upfront choices. More than once, a major investigation traced failures back to a low-grade starting material. Strong supply chains don’t leave these decisions up to chance.
As chemical sourcing continues to globalize, end users rely increasingly on transparency and documented quality. With this compound, stability data, repeatable performance metrics, and supply assurance factor heavily into purchasing decisions. End-users benefit from open communication about production methods and analytical controls. Whether working in a university setting or a corporate innovation center, researchers should have clear access to batch records and a trusted supply.
Digitalization in supply management also changes the landscape. Inventory systems link lab benches to procurement teams and even directly to synthesis reactors. Real-time quality reporting closes long-standing gaps between end-users and suppliers. The right intermediate, well-documented and consistently pure, speeds up the cycle from idea to product.
On the horizon, more sustainable synthesis routes continue to evolve. Suppliers who offer 4-Chlorobenzonitrile from renewable feedstocks or low-waste technologies attract strong interest. In my own networks, colleagues swap notes on greener sourcing every chance they get, citing both institutional and customer demand for improved lifecycle impacts.
The chemists who work with these intermediates regularly know their worth. Online forums and professional societies provide ample evidence that 4-Chlorobenzonitrile ranks among the backbone reagents of aromatic chemistry. Open-access case studies, technical presentations, and peer-reviewed articles all point to repeatable success stories driven by high-purity lots.
While expert commentary often homes in on advanced end-uses, practical experience in undergraduate labs drives home the basics just as powerfully. Many instructors quietly reroute budgets to stable, high-purity sources, knowing the impact this has not only on yield, but also on the educational value and reproducibility of experiments.
From a larger viewpoint, the growing demand for transparent, documented chemistry drives improvements up the supply chain. Clean, well-characterized 4-Chlorobenzonitrile supports both reliable science and public trust in the field as a whole.
As discovery timelines shrink and regulatory standards climb, the margin for error narrows. Sourcing high-purity 4-Chlorobenzonitrile directly addresses this challenge. Rather than experimenting with cheaper or less-documented alternatives, research and manufacturing teams shift toward suppliers who back their claims with clear, reproducible data. Auditable trails, accessible certificates of analysis, and responsive technical support close gaps that previously slowed innovation.
Even with all the advances, work remains to expand access and awareness. Not every lab—especially those in resource-limited settings—has the ability to prioritize the highest-purity intermediates. By sharing case studies and advocating for broad supply chain integrity, the broader community moves the whole field forward.
Looking back at years spent working across research, process development, and instruction, the foundational role of reliable intermediates stands out. 4-Chlorobenzonitrile—a simple compound with a reputation for high purity—quietly anchors research projects, accelerates scale-ups, and supports safer, cleaner operations. Its consistency saves time, energy, and resources, all while enabling scientific and technical progress.
The shift toward high-quality, well-documented chemical sourcing is no passing trend. It reflects a deeper realization—across disciplines and industries—that lasting results depend on upfront choices. For those creating the medicines, materials, and technologies of tomorrow, investing in trustworthy, high-purity 4-Chlorobenzonitrile is more than a procurement decision; it’s a statement of intent for quality, safety, and impact.