|
HS Code |
577243 |
| Chemical Name | 2-Hydroxy-3-pyridinecarbonitrile |
| Molecular Formula | C6H4N2O |
| Molecular Weight | 120.11 g/mol |
| Cas Number | 50487-99-7 |
| Appearance | White to off-white solid |
| Melting Point | 170-174°C |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
| Smiles | C1=CC(=C(N=C1)O)C#N |
| Inchi | InChI=1S/C6H4N2O/c7-3-5-4-8-2-1-6(5)9/h1-2,4,9H |
As an accredited 2-Hydroxy-3-Pyridinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100-gram amber glass bottle with tamper-evident cap, labeled "2-Hydroxy-3-Pyridinecarbonitrile, 98%," includes safety and handling information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Hydroxy-3-Pyridinecarbonitrile: typically 10–12 metric tons, packed in 25 kg fiber drums, on pallets. |
| Shipping | 2-Hydroxy-3-pyridinecarbonitrile is shipped in tightly sealed containers, protected from moisture and light. It is typically transported as a solid at ambient temperature, following standard chemical safety regulations. Labels indicating hazard classification are provided, and shipments comply with relevant national and international transportation requirements for laboratory chemicals. |
| Storage | **2-Hydroxy-3-Pyridinecarbonitrile** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep the chemical away from incompatible substances such as strong oxidizers and acids. Protect it from direct sunlight, moisture, and sources of ignition. Follow all applicable safety regulations and ensure proper labeling and secure storage to prevent accidental spillage or misuse. |
| Shelf Life | 2-Hydroxy-3-pyridinecarbonitrile typically has a shelf life of 2–3 years when stored in a cool, dry, and airtight container. |
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Purity 99%: 2-Hydroxy-3-Pyridinecarbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal reaction yield. Melting Point 140°C: 2-Hydroxy-3-Pyridinecarbonitrile with a melting point of 140°C is used in fine chemical manufacturing, where controlled melting behavior contributes to process stability. Particle Size <50 microns: 2-Hydroxy-3-Pyridinecarbonitrile with particle size less than 50 microns is used in catalyst formulation, where fine particle distribution enhances catalytic surface area. Moisture Content <0.2%: 2-Hydroxy-3-Pyridinecarbonitrile with moisture content below 0.2% is used in agrochemical synthesis, where low moisture minimizes unwanted side reactions. Stability Temperature up to 180°C: 2-Hydroxy-3-Pyridinecarbonitrile stable up to 180°C is used in high-temperature organic synthesis, where thermal stability maintains compound integrity. Residual Solvents <500 ppm: 2-Hydroxy-3-Pyridinecarbonitrile with residual solvents less than 500 ppm is used in specialty dye production, where reduced solvent content prevents contamination of final products. Bulk Density 0.65 g/cm³: 2-Hydroxy-3-Pyridinecarbonitrile with bulk density 0.65 g/cm³ is used in formulation of dry powder blends, where consistent density ensures uniform mixing. Assay ≥98.5%: 2-Hydroxy-3-Pyridinecarbonitrile with assay not less than 98.5% is used in research laboratory applications, where high assay supports reproducible experimental results. Chromatographic Purity ≥99%: 2-Hydroxy-3-Pyridinecarbonitrile with chromatographic purity of at least 99% is used in analytical reference standards, where high purity guarantees accurate calibration. Heavy Metal Content <10 ppm: 2-Hydroxy-3-Pyridinecarbonitrile with heavy metal content below 10 ppm is used in electronic chemical manufacturing, where low metal impurities reduce risk of device failure. |
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Chemistry often brings together practicality and precision. In the field of organic synthesis, few compounds capture this balance the way 2-Hydroxy-3-Pyridinecarbonitrile does. I remember my first introduction to this molecule back in grad school, surrounded by glassware and the faint smell of pyridine. This compound—sometimes called 2-hydroxynicotinonitrile—offers more than just a string of atoms. It provides a reliable backbone for research labs, pharmaceutical work, and process industries seeking predictable results from a building block they can trust.
With a structure built around a pyridine ring, accented by a hydroxy group and a nitrile function, it’s no surprise 2-Hydroxy-3-Pyridinecarbonitrile has earned its place in the synthetic chemist’s toolkit. The molecule, formula C6H4N2O, embraces versatility—supporting reactions from functionalization to cyclization, making it useful across multiple branches of chemistry.
In practical terms, what buyers look for circles back to model, purity, and storage. Labs hunting for consistency gravitate to batches with purity greater than 98%. Not every source offers this level; those that cut corners with lower grades leave researchers troubleshooting side reactions or re-purifying intermediates. Each lab run or scale-up that skips a proper purity check risks unreliable outcomes. Simple lessons learned from sharing a bench: higher purity means fewer headaches, less backtracking, more time spent on what matters.
Model numbers or lot codes can help trace batches and guarantee reproducibility. Some products use alphanumeric codes tying back to synthesis date, storage conditions, or even starting material provenance. This traceability doesn’t just please auditors or regulators; it directly supports day-to-day work. Think of troubleshooting a failed reaction. It’s frustrating enough without having to chase down ambiguous lot histories or guess at lurking decomposition. Verified model and lot tracking are not just regulatory boxes—they’re peace of mind for anyone who cares about data integrity.
As for storage, the hydroxy and nitrile groups demand respect. Even the best batch can lose reliability if stored exposed to moisture or ambient light for months. I’ve learned that sealed, amber-glass containers in temperature-stable cupboards beat open shelves every time. The compound’s resilience means shelf life is generous under proper conditions, but slight lapses invite polymerization or hydrolysis. Anything less than best practices ends up as extra work or unexpected byproducts downstream.
Comparing this molecule to others in the pyridine family offers some perspective. Pyridinecarbonitriles pop up in countless catalogues, but swapping the hydroxy group from position two to four—or omitting it altogether—shifts both reactivity and utility. In my own experiments, the ortho hydroxy and nitrile combination on a six-membered aromatic ring drives selectivity. These functional groups don’t just sit for show—they help direct subsequent substitutions and open up a variety of coupling possibilities. Chemists lean into this predictability when designing syntheses for complex targets.
It’s not enough to assess a compound by name or family. Isomers matter, and so does functionalization. For instance, 4-hydroxypyridinecarbonitrile shares a root but invites very different reactivity. Even comparing with 2-chloro-3-pyridinecarbonitrile underlines how a simple swap—hydroxy for chloro—can mean a difference in solubility, hydrogen bonding potential, and downstream reactivity. I recall screening both for a custom ligand synthesis; one set of conditions worked beautifully for 2-hydroxy, stubbornly failed with the 2-chloro. These differences reinforce how choosing the right building block sets the tone for an entire project.
For some, price becomes the main concern, but experienced labs know that reliability pays off. A 2-Hydroxy-3-Pyridinecarbonitrile batch from a trusted supplier produces robust, reproducible results. It supports scale-up, analytical method development, and regulatory filings with confidence. Saving a fraction with an off-grade batch almost always costs more in repeat experiments and wasted hours.
What keeps this compound in demand boils down to its many roles. Early in my career, I saw it as a stepping stone for pharmaceutical syntheses. The hydroxy group opens doors for ether and ester formation, while the nitrile handles straightforward transformations to amides, acids, or even heterocyclic frameworks. Drug discovery teams rely on its dual functionality—enabling scaffold decoration and allowing for further elaboration in a single step.
Chemical process engineers find value too. Small tweaks with this intermediate can build out flavors, agrochemicals, or specialty dyes. Whether as a core scaffold or a tailored intermediate, 2-Hydroxy-3-Pyridinecarbonitrile adapts to both high-throughput screening and production runs. Working with a team focused on developing a new herbicide, I saw the molecule anchor critical synthetic steps thanks to its predictable reactivity and work-up simplicity.
Academic labs often chase novelty, designing new reactions or probing reactivity under different catalytic conditions. Here, 2-Hydroxy-3-Pyridinecarbonitrile acts as a test case. It responds to diverse conditions, revealing subtle influences from solvent, catalyst, or temperature. These lessons travel from journal articles straight into industrial process optimization, a bridge that keeps fundamental research rooted in real-world effect.
Beyond pharmaceuticals and fine chemicals, material scientists take advantage of pyridine rings for specialty polymers or electronic materials. The hydroxy group lets researchers assemble larger, conjugated systems, while the nitrile stabilizes the scaffold against breakdown. The range of published literature illustrates this versatility. When searching for a robust, adaptable starting material, this compound earns its place at the front of the line.
Even with its popularity, not every purchase goes smoothly. I’ve seen supply chain hiccups—purity inconsistencies, documentation gaps, even outright mislabeling. This isn’t just an inconvenience. In regulated settings, one misstep in sourcing can upend months of validation. One colleague received an off-spec batch and didn’t catch the error until final analysis, leading to a scramble to identify the issue and a painful reset of the project timeline. The lesson carries weight: never take quality for granted. Ask the questions that matter, cross-check purity, and look for certificates of analysis traceable to respected laboratories.
Handling and safety come next. Pyridines often carry a sharp, biting smell few forget. The toxicity profile parallels that of related nitriles, requiring care in both personal handling and disposal. Fume hoods, gloves, and routine environmental controls are basic expectations—not special precautions. Well-run facilities treat all pyridines with respect, but familiarity sometimes breeds complacency. Regular training and easy access to safety information remain simple fixes that pay big dividends.
Transport and storage logistics can complicate matters. Even small changes—like choosing plastic over glass containers—make long-term differences. Light, humidity, and air exposure trigger slow changes most users miss until analytical checks catch the drift. I’ve worked in facilities where simple upgrades—amber bottles, nitrogen atmosphere, controlled access storage—extended the working life of bulk supplies and ensured clean reactions month after month.
It’s tempting to cut corners in procurement or ignore subtle batch differences in pursuit of speed or price savings. Here’s the reality: every careless shortcut gets paid back with interest. For regulated industries—pharma, crop science, materials—the supplier’s reputation and documented history matter as much as the box on the delivery cart.
True, some smaller operations get by with less rigorous support. But for larger organizations and grant-funded labs, consistent documentation, repeatable quality, and transparency in supply chain reporting are non-negotiable. Anyone who’s been through a regulatory audit will appreciate the value of complete traceability and a stack of clear certificates. In a world where supply disruptions, counterfeit products, or breakdowns in component quality can stall teams for weeks, confidence grows from a history of reliability.
I have seen teams trial and error their way through unreliable starting materials, only to return to trusted brands and pay the extra for the certainty that a critical run won’t go sideways because the building block didn’t meet specs. This trust isn’t built overnight. It grows from years of standardized testing, batch-to-batch reproducibility, and a willingness to replace or recall when things don’t meet the bar. Adherence to robust production and documentation protocols is not about bureaucracy; it’s about ensuring every downstream process works as planned—leaving the scientist focused on innovation, not damage control.
Another reason 2-Hydroxy-3-Pyridinecarbonitrile has found lasting value comes from its role in supporting greener, more resource-conscious processes. Unlike some specialty intermediates, its synthesis often avoids harsh conditions or toxic metal catalysts. As pressure builds on manufacturers to reduce environmental footprints, interest in cleaner synthetic routes and lower-waste processes has grown. Some suppliers now emphasize compliance with green chemistry principles and invest in purification technologies that cut solvent and energy use.
Regulatory frameworks across Europe, North America, and Asia have grown sharper. This isn’t just about environmental impact. End users want materials that arrive with transparent reporting—MSDS sheets, source documentation, and batch certificates traceable to audited labs. I remember the difference this made in an international technology transfer: regulatory officers cleared shipments more quickly, and the team moved from bench to pilot scale knowing every bottle was accounted for. With the right paperwork and full traceability, even tough jurisdictional hurdles become manageable.
Waste handling, too, factors into the discussion. 2-Hydroxy-3-Pyridinecarbonitrile offers relative stability, allowing for straightforward containment and neutralization procedures. Companies invested in resource stewardship appreciate its low environmental persistence and amenability to established disposal methods—a practical edge as ecological responsibility grows from voluntary to mandatory practice.
Looking at the current research landscape, 2-Hydroxy-3-Pyridinecarbonitrile continues to inspire new chemistry. Its presence in medicinal chemistry plays out in the patent literature. Analogues built around its core scaffold target antimicrobial, anti-inflammatory, and enzyme inhibitory activities. Whether in the hands of a startup or a pharmaceutical giant, the molecule allows for rapid exploration of chemical space, helping drive the search for new therapeutic leads.
Material chemists explore its use for constructing solid-state networks or functional coatings. The hydroxy group brings pathways to surface anchoring, while the nitrile supports polymer attachment or further derivatization. My own introduction to material applications came through a collaboration targeting organic electronics, and this molecule offered the adaptability needed for both device performance and process reliability.
The continuing trend towards modular, fragment-based synthesis highlights the value of starting materials that bridge reactivity, cost, and practical work-up. 2-Hydroxy-3-Pyridinecarbonitrile brings all three to the table. While most academic research tends to focus on the newest, shiniest targets, teams with experience know the value in returning to reliable materials—especially as demands for scale, safety, and sustainability grow.
AI-driven retrosynthetic analysis and automated flow chemistry have changed the approach to route design in many companies. Having consistent, well-documented building blocks like this one simplifies the transition from computational target to real-world compound. As experiments scale or speed up, the compound’s consistency makes it easier to troubleshoot, replicate, and optimize processes—giving chemists more space to experiment instead of troubleshooting avoidable errors.
No product operates in a vacuum. Procurement challenges, quality fluctuations, storage mishaps—they’re all part of the day-to-day lab environment. The best advice comes from learning by doing. Choose suppliers that publish and uphold batch specifications, openly share detailed certificates of analysis, and answer technical queries with specificity, not generic statements. This builds a foundation of trust and allows users to catch issues before they reach the fume hood.
Despite improvements in manufacturing, information gaps persist. Some organizations still issue thin documentation or fail to communicate lot-to-lot changes. One possible fix involves closer collaboration between buyer and supplier. A responsive technical team bridges many gaps. I’ve found value in regular site visits and virtual audits, where end users can watch production or review quality assurance protocols. While this may sound time-consuming, the cost pales compared to an extended process shutdown due to a batch inconsistency.
Labs can further reduce the risk of degraded or contaminated stock with basic protocols: date and label every container opened, log temperatures in storage areas, test randomly sampled material periodically. Regular review of inventory and planned consumption schedules goes far—especially in environments where batch-to-batch consistency underpins published results or clinical trial material.
For safety and compliance, make sure current MSDS documentation is accessible everywhere the compound is in use, and coordinate with environmental teams on disposal standards. Encourage open discussions of near-misses or process hiccups—creating an environment where team members learn from scratches and spills, rather than repeat them.
Collaboration isn’t only for troubleshooting. Some of the most innovative advances spring from supplier and customer development partnerships. Feedback on process pain points, unique application needs, or new product requirements often leads to enhanced purification techniques, packaging upgrades, or even custom grades designed for niche industries. For teams engaged with 2-Hydroxy-3-Pyridinecarbonitrile over many years, shared learning yields real improvements—saving money, time, and waste alike.
Reflecting on my own years in the lab, what stands out is not the novelty of 2-Hydroxy-3-Pyridinecarbonitrile but its reliability. This is a compound that keeps the wheels of discovery turning, lets chemists chase new molecules with confidence, and holds up under the scrutiny of peer review and regulatory inspection. The field’s move toward “greener” chemistry and responsible sourcing gives it an enduring spot in both academic and industrial settings.
Like any specialized material, it’s what you do with it that matters most. Prioritizing quality, transparency, and best practice in handling transforms a simple batch of powder into a foundation for discovery and innovation. As research becomes more global and collaborative, the value only grows from products that foster trust, deliver consistency, and make it easier to move from idea to impact.