|
HS Code |
927288 |
| Name | Pyridine-3-carbonitrile |
| Other Names | 3-Cyanopyridine |
| Chemical Formula | C6H4N2 |
| Molar Mass | 104.11 g/mol |
| Cas Number | 100-54-9 |
| Appearance | White to pale yellow solid |
| Melting Point | 52-54°C |
| Boiling Point | 220-222°C |
| Density | 1.16 g/cm³ |
| Solubility In Water | Moderately soluble |
| Flash Point | 113°C |
| Smiles | C1=CC(=CN=C1)C#N |
| Pubchem Cid | 7844 |
| Refractive Index | 1.524 at 20°C |
As an accredited Pyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 500g Pyridine-3-carbonitrile is packaged in a sealed, amber glass bottle with a secure screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Pyridine-3-carbonitrile is typically loaded in 200kg drums, totaling approximately 80 drums (16 MT) per 20′ FCL. |
| Shipping | **Pyridine-3-carbonitrile** should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Store in a cool, well-ventilated area, away from sources of ignition. Clearly label packages and comply with all applicable local, national, and international transport regulations, as it may require classification as a hazardous chemical during shipping. |
| Storage | Pyridine-3-carbonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. It should be kept separate from strong oxidizing agents and acids. Use appropriate safety containers and clearly label them. Avoid moisture exposure, and always follow local regulations for hazardous chemical storage. |
| Shelf Life | Pyridine-3-carbonitrile typically has a shelf life of 2 years when stored in tightly sealed containers, away from heat and moisture. |
|
Purity 99%: Pyridine-3-carbonitrile 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimal impurity formation. Melting point 82°C: Pyridine-3-carbonitrile with a melting point of 82°C is used in active pharmaceutical ingredient (API) manufacturing, where controlled phase transitions enable precise formulation consistency. Particle size ≤10 µm: Pyridine-3-carbonitrile with particle size ≤10 µm is used in fine chemical catalysis, where enhanced surface area accelerates reaction rates. Stability up to 120°C: Pyridine-3-carbonitrile stable up to 120°C is used in process-scale organic synthesis, where thermal stability maintains product integrity under reaction conditions. Moisture content <0.1%: Pyridine-3-carbonitrile with moisture content below 0.1% is used in high-sensitivity analytical chemistry, where low water content reduces unwanted side reactions. Assay ≥98.5%: Pyridine-3-carbonitrile with assay above 98.5% is used in agrochemical formulation, where assay reliability supports consistent product performance. Residual solvents <500 ppm: Pyridine-3-carbonitrile with residual solvents under 500 ppm is used in electronic materials synthesis, where minimal contamination preserves dielectric properties. |
Competitive Pyridine-3-carbonitrile prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Pyridine-3-carbonitrile, often recognized by its chemical structure of a pyridine ring attached to a cyano group at the third position, has drawn attention throughout the scientific and manufacturing communities. The specific positioning of the cyano group plays a crucial role in the compound’s reactivity, separating it from similar pyridine derivatives. Chemists and technicians pay close attention to the consistency of the compound’s molecular weight and physical form, which typically presents as a pale crystalline substance. Unlike some pyridine compounds that have a sharp and unpleasant odor, pyridine-3-carbonitrile often carries a milder scent, reducing the discomfort during handling.
Diving into laboratory routines, handling this compound involves straightforward techniques. Most practitioners observe that its solubility in common organic solvents like methanol and ethanol allows for easy preparation of working solutions, whether in research or in pilot synthesis operations. Its melting point, usually sitting above room temperature, provides stability during storage, especially if the work environment lacks climate control. This reliable stability preserves product integrity, which I have found invaluable when conditions shift or inventory sits longer than expected.
Manufacturers typically offer pyridine-3-carbonitrile in several grades, with high-purity options catering to pharmaceutical synthesis and slightly lower grades supporting agricultural or material science research. Concentrating on the model that achieves above 99% purity, labs secure predictable reaction outcomes, leading to cost-effective development cycles. Glass bottles and high-density polyethylene containers dominate packaging for this compound, both materials shielding contents from incidental moisture and minimizing light exposure. Working with these containers saves time otherwise spent checking for leaks or contamination.
From my own experience coordinating with suppliers, purity levels and shelf life influence project timelines. Twice I have compared batches from different storage vessels, noticing a clear difference where glass containers kept the product free from slight yellowing, while the plastic variants sometimes showed minor discoloration if not kept away from sunlight. It demonstrated to me that packaging does more than protect a product; it keeps research on track and reduces waste due to spoilage.
Exploring the market, this compound carves out a special place in pharmaceutical research. Chemists rely on pyridine-3-carbonitrile as a building block in drug development, contributing both the structural rigidity of its six-membered ring and the potential for further modification at the cyano position. Novel antibiotics, anti-inflammatory agents, and even some therapies addressing neurodegenerative disorders start their journey with pyridine-3-carbonitrile at the foundation.
The compound’s advantage stretches beyond the pharmaceutical sector. Industrial chemists use it to generate dyes, even some advanced polymers that must perform reliably at higher temperatures. In agrochemical synthesis, I have seen reports of pyridine-3-carbonitrile helping formulate selective herbicides that minimize off-target effects, aligning with modern expectations for environmentally conscious farming solutions. These applications depend on the predictable reactivity of the cyano group – a point that often saves time during multi-step syntheses where yield and selectivity matter.
Comparing workflows, this chemical becomes a workhorse during heterocyclic compound construction. Its straightforward reactivity pattern eliminates time-consuming side-product separation, a factor anyone managing tight production schedules will appreciate. The directness with which it undergoes nucleophilic substitution and coupling reactions streamlines the path to finished products, helping both large-scale manufacturers and academic researchers avoid bottlenecks in their timelines.
The world of pyridine derivatives spans a crowded field, yet pyridine-3-carbonitrile draws clear boundaries by offering a different balance between reactivity and stability. In comparison, pyridine-2-carbonitrile and pyridine-4-carbonitrile both see use in similar fields, yet changing the position of the cyano group impacts their chemical pathways significantly. I noticed, for instance, that electrophilic substitution at the meta position on pyridine rings usually proceeds with lower side reactions when compared to the ortho or para forms. This practical distinction means fewer purification steps, less solvent usage, and trimmed-down waste management requirements in both small-scale labs and commercial settings.
Some products with similar structures present more aggressive or irritating vapors, pushing users toward elaborate fume hood procedures or extra protective gear. Working with pyridine-3-carbonitrile reduces these hurdles, provided baseline safety routines are followed. This accessibility widens the user base to include institutions with less infrastructure, such as teaching labs or startups working on a shoestring budget. For me, having encountered situations where overbearing fumes led to complaints and workflow interruptions, the adoption of compounds with a milder profile restored productivity and improved morale.
Research and manufacturing demand traceability. Pyridine-3-carbonitrile, especially at higher purity, is typically supported by a robust certificate of analysis. From experience, I know that having full transparency into batch history, impurity profiles, and lot consistency prevents last-minute surprises in sensitive projects. Analytical support in the form of NMR, HPLC, and IR data builds confidence, and suppliers who can promptly answer questions about production methods tend to win repeat business.
While not strictly governed as a controlled substance, this compound must meet safety and environmental standards before it enters critical supply chains. Stringent adherence to guidelines for handling, storage, and waste disposal remains non-negotiable, both for compliance and for personal safety. Institutional safety data sheets detail hazard classes and personal protective equipment recommendations, forming a comprehensive roadmap for risk minimization. In my work, early attention to ventilation, spill procedures, and emergency access plans ensured smooth audits and, more importantly, protected personnel and property from preventable accidents.
Everyone in the business of buying chemicals faces the balancing act of cost and supply reliability. Over the years, I have tracked periods where upstream shortages of starting materials nudged prices upward, briefly prompting the search for substitutes or alternative procurement strategies. Smaller manufacturers occasionally flirt with inconsistent quality, but the larger, established suppliers invest in process control–minimizing run-to-run variance, a critical point for organizations needing scalable and reproducible outcomes.
In recent years, disruptions in logistics networks have spotlighted the value of local and regional manufacturing. Labs opting for suppliers that produce pyridine-3-carbonitrile on the same continent often encounter faster turnaround times and reduced customs hurdles. During an episode where international shipping brought one of my projects to a halt for several weeks, it became obvious how domestic sourcing delivered real advantages. Transparent supply chains, regular communication with sales reps, and access to technical support do more than smoothen purchases — they keep careers and research objectives moving forward.
Real-world use brings hands-on challenges. While working with pyridine-3-carbonitrile, static electricity and low ambient humidity can cause minute spills or dusting during scale-up or transfer between containers. Solutions include installing antistatic mats, grounding metal equipment, and wearing appropriate gloves that double as both chemical and static barriers. Training teams to recognize these conditions, instead of treating spills as rare accidents, builds a more prepared and responsive work culture.
Temperature swings influence both storage and transportation. Most supply rooms maintain a moderate, dry environment, and operators avoid opening containers in high humidity where possible. Focusing on small, airtight packs rather than bulk drum storage cuts down the risk of repeated exposure, which gradually degrades the compound as much as it threatens user safety. I have seen projects stall when an overlooked cap led to moisture ingress over a long weekend, reinforcing the value of routine checks and investment in quality seals.
Concerns about sustainability have not skipped the chemical sector, and pyridine-3-carbonitrile’s use demands clear-eyed waste planning. While relatively stable, its disposal requires incineration or treatment by licensed facilities rather than simple landfill or drain disposal. Some organizations attempt to recover or recycle unused material, either by purification or conversion into less hazardous compounds. These programs reduce cost and minimize burdens on environmental systems.
The shift toward closed-loop chemical management draws momentum from both regulatory changes and communal pressure to reduce laboratory waste. Directly observing labmates embrace greener protocols – like consolidating waste streams or substituting greener solvents during cleaning – led me to reconsider old habits. Switching to water-based decontamination where feasible, as well as joining in on waste-reduction campaigns, shrinks the environmental impact and sets new expectations for responsible chemical stewardship.
Pyridine-3-carbonitrile’s role continues to evolve with advances in synthetic and computational chemistry. Machine learning models now help predict new reaction pathways and optimize yield for pharmaceutical precursors, shifting the way researchers approach compound design. Automated reactors and precision dosing equipment further streamline processes, as seen in labs that scale from milligram to kilogram without pausing to revalidate each step. The combination of computational prediction and hands-on, high-throughput synthesis marks a new era for this compound’s adoption in research.
Collaborations between academic researchers and commercial producers support a constant flow of feedback, raising both productivity and product performance. These partnerships sometimes lead to custom formulations or blends designed to meet novel technical specifications, such as improved solubility or tailored reactivity for specific downstream processes. Keeping both communication and records open brings confidence and encourages the sharing of best practices, which accelerates discovery.
As usage widens, the gap in formal training grows apparent. Not every organization provides comprehensive onboarding for chemical handling, storage, and reaction safety. To reduce avoidable mishaps, teams benefit from peer mentoring, on-site demonstrations, and accessible online resources. Supporting a culture where questions flow freely and every team member feels responsible for safe practice pays long-term dividends.
My own early missteps while scaling up synthesis batches taught respect for measured, stepwise progression. Skipping safety checks due to overconfidence led to a minor spill, proving that careful review of reaction plans should anchor every operation with this compound, no matter how routine the task seems. Building routine checklists and fostering a learning environment raise the collective baseline for both safety and process efficiency.
Sectors such as clean energy and electronics engineering increasingly borrow compounds like pyridine-3-carbonitrile for novel uses. Coatings, sensors, and specialty batteries sometimes rely on derivatives that demand both purity and consistency at scale. As industries converge and share knowledge, feedback loops spring up that drive progress in purification, logistics, and even greener synthesis routes. Firms investing in continuous improvement help raise the standard for both product quality and environmental responsibility.
Global business uncertainty—from trade tensions to emerging regulatory frameworks—impacts production and supply security. Observing trends, many organizations build dual sourcing arrangements or maintain modest inventory reserves as insurance against unforeseen disruptions. Investing in strong supplier relationships and staying informed about upstream pressures offers real-world leverage that softens the blow of market shocks.
Modern buyers increasingly favor suppliers who welcome scrutiny. Open sharing of batch data, supply traceability, and compliance history shows commitment to transparency. Digital platforms tracking lot movement, real-time purity metrics, and incident response records offer peace of mind that blends tradition with modern capability. From personal observation, these layers of documentation cut back on both communication errors and costly rework, anchoring project reliability in clear, accurate data.
Pyridine-3-carbonitrile’s success in both research and industry comes down to trust—in the product, the people handling it, and in the supply channels delivering it. Knowledge sharing, responsible stewardship, and an adaptable mindset combine to shape a field ready for tomorrow’s challenges. Long-term investment in staff training and infrastructure, as well as meaningful dialogue between stakeholders, keeps innovation flowing while reducing waste and ensuring safe practices.
Continued attention to real-world challenges and a willingness to adjust protocols foster resilience. In the ever-changing world of chemical production and use, this approach keeps projects on track, safeguards teams, and makes responsible use of every gram of pyridine-3-carbonitrile.