|
HS Code |
292930 |
| Chemical Name | 2-Cyano-5-hydroxypyridine |
| Cas Number | 5444-77-7 |
| Molecular Formula | C6H4N2O |
| Molar Mass | 120.11 g/mol |
| Appearance | Off-white to yellowish powder |
| Melting Point | 150-154 °C |
| Solubility In Water | Slightly soluble |
| Synonyms | 5-Hydroxy-2-cyanopyridine |
| Pubchem Cid | 89398 |
| Inchi Key | UYRLVTZXZLNHKF-UHFFFAOYSA-N |
| Smiles | C1=CC(=NC=C1C#N)O |
| Storage Conditions | Store in a cool, dry, well-ventilated place |
| Hazard Statements | Irritant |
As an accredited 2-CYANO-5-HYDROXYPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g of 2-Cyano-5-hydroxypyridine comes in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL: Typically loaded with 480 drums (25 kg each) of 2-CYANO-5-HYDROXYPYRIDINE, totaling 12 metric tons per container. |
| Shipping | 2-Cyano-5-hydroxypyridine is typically shipped in sealed, chemical-resistant containers under ambient conditions. It should be clearly labeled, securely packaged, and handled according to standard hazardous material protocols. Transport complies with local, national, and international regulations to ensure safe delivery and to prevent contamination, spills, or exposure during transit. |
| Storage | 2-Cyano-5-hydroxypyridine should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect the chemical from moisture and direct sunlight. Ensure proper labeling and limit exposure to air. Store at room temperature and follow standard safety procedures for handling organic chemicals. |
| Shelf Life | 2-Cyano-5-hydroxypyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and tightly sealed container. |
|
Purity 98%: 2-CYANO-5-HYDROXYPYRIDINE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 172°C: 2-CYANO-5-HYDROXYPYRIDINE with a melting point of 172°C is applied in fine chemical manufacturing, where it enables consistent solid-state reaction processing. Molecular Weight 136.12 g/mol: 2-CYANO-5-HYDROXYPYRIDINE at a molecular weight of 136.12 g/mol is utilized in agrochemical research, where precise formulation control is achieved. Stability Temperature 120°C: 2-CYANO-5-HYDROXYPYRIDINE stable up to 120°C is incorporated in heterocyclic compound development, where it maintains compound integrity during synthesis. Particle Size <50 µm: 2-CYANO-5-HYDROXYPYRIDINE with particle size less than 50 µm is employed in catalyst preparation, where it promotes uniform distribution and enhanced catalytic activity. UV Absorbance 254 nm: 2-CYANO-5-HYDROXYPYRIDINE with strong UV absorbance at 254 nm is used in analytical reference standards, where it provides reliable quantification accuracy. Moisture Content <0.5%: 2-CYANO-5-HYDROXYPYRIDINE with moisture content below 0.5% is utilized in high-purity material applications, where it prevents hydrolysis and degradation. Solubility in DMSO: 2-CYANO-5-HYDROXYPYRIDINE soluble in DMSO is applied in medicinal chemistry screening, where it enables high-concentration compound testing. |
Competitive 2-CYANO-5-HYDROXYPYRIDINE 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!
Every laboratory shelf tells a story. Tucked between weathered glassware and stacks of research journals, certain chemicals quietly do the heavy lifting in innovation. One compound catching more attention in the synthesis world is 2-Cyano-5-Hydroxypyridine. For folks engaged in pharmaceutical research or anyone who has spent hours tracking down rare intermediates, having access to a consistent, well-characterized product like this can feel like finding an old tool you know you can trust.
Specifically, 2-Cyano-5-Hydroxypyridine crops up in labs driving forward drug discovery and agrochemical innovation. Its clean structure—anchored by a pyridine ring, a hydroxyl group at the 5-position, and a cyano group at the 2-position—offers something most generic intermediates don’t: a smart balance of reactivity and selectivity. Over the years, chemists have found plenty of stories woven through procedures involving this molecule, where a challenging transformation became possible or an unexpected breakthrough appeared amid columns and TLC plates.
What draws many teams to this compound is the level of detail that goes into preparation and quality control. A well-documented batch of 2-Cyano-5-Hydroxypyridine typically presents as a crystalline or powdery solid, its pale appearance aligning with documented literature. In the trade, purity above 98% is not just a nicety—it’s an essential. Stringent HPLC and NMR analysis often back up the data, ensuring the product doesn’t introduce noise or confusion during complex syntheses. Unlike the days when chemists worried about batch-to-batch variation, consistent analytical results have shifted 2-Cyano-5-Hydroxypyridine into the column of genuinely reliable intermediates.
Melting point, solubility profile, and moisture content all shape how researchers integrate this product into their workflow. I’ve seen researchers lose days tweaking reaction conditions only to find the problem started with a poorly characterized intermediate. In this context, knowing the exact melting point and spectrum helps ensure that work moves forward without stumbling over surprising impurities or unidentified side products. Simple details—good documentation, reliable melting range, solid spectral data—give labs peace of mind and save time.
Academic groups and industry researchers approach 2-Cyano-5-Hydroxypyridine for slightly different reasons, but the underlying driver is the same: versatility. In pharmaceutical research, it has grown popular in the synthesis of heterocyclic scaffolds. Many medicinal chemists recognize its cyano and hydroxy functionality as adaptable handles—points where further elaboration becomes straightforward, whether one is building out ring systems for kinase inhibitors or preparing custom ligands for biochemical probing.
On the agrochemical front, this compound helps streamline the path to novel pesticide motifs. Pyridine derivatives play a central role in the molecules that end up on crop fields, and introducing strong functional groups like cyano and hydroxy opens up a range of creative synthetic pathways. For both small operations and larger R&D outfits, having a reliable supply means teams focus energy on optimizing their lead compounds rather than troubleshooting intermediate quality.
Even beyond pharma and agriculture, specialty chemical companies look to 2-Cyano-5-Hydroxypyridine when seeking unique dye components, crosslinking agents, or functional materials for the lab and industry. Its molecular backbone adapts well in multi-step syntheses, something any seasoned organic chemist values. This flexibility saves time, reduces waste, and removes some of the unpredictability from project schedules.
Picking the right reagent often comes down to chemistry, cost, and dependability. Compared to similar pyridine derivatives, 2-Cyano-5-Hydroxypyridine stands out for the way it combines a responsive cyano group with a modifiable hydroxyl. Other compounds in its class—say, 2-Cyanopyridine on its own—lack the additional oxygen, making certain subsequent reactions more cumbersome. A 5-hydroxy group doesn’t just open up distinct hydrogen-bonding and metal-coordinating pathways, it also streamlines steps like alkylation, esterification, or even oxidation.
This mix of features makes the molecule a kind of Swiss army knife for those aiming to tailor bioactive molecules. Structurally, it lets researchers navigate synthetic challenges that more symmetric, less functionalized pyridine cores can’t address. Many teams have remarked that, with this scaffold in hand, routes to specific targets snap into place more naturally. These efficiencies don’t show up on a cost sheet but play out in real savings over a project’s lifetime—saving on solvents, chromatographic separations, and even labor hours.
Not all intermediates offer this combination of reactivity and stability. 2-Cyano-5-Hydroxypyridine holds up well under varied lab conditions and resists the pitfalls of high moisture or temperature, which knocks some competing substances out of contention. You avoid those headaches where a batch decomposes overnight or gums up equipment, real issues with less stable options like 2-Aminopyridine or certain substituted pyrazoles.
Whether combing through published reaction schemes or speaking directly with process chemists, it’s clear that the compound’s reputation is not built on theory alone. Published yields and selectivities track favorably against alternate starting materials. For example, studies in heterocyclic chemistry highlight improved ring-closing efficiency and cleaner product profiles with 2-Cyano-5-Hydroxypyridine. In my own experience collaborating on urea derivative projects, downstream purification ran smoother thanks to fewer chromatographic challenges when this compound was chosen over close analogs.
From a quality assurance perspective, trusted sources publish clear analytical fingerprints: sharp NMR singlets, predictable IR stretching bands, consistent HPLC retention. Given the rising expectations for regulatory compliance, especially in pharma and agrochemical settings, such transparency enables approval processes to move forward without lengthy back-and-forth. Strong documentation has helped research teams minimize risk and avoid product recalls tied to off-specification materials.
Even reliable intermediates aren’t immune to improvement. Handling and storage requirements top the list of day-to-day concerns. Though 2-Cyano-5-Hydroxypyridine proves more stable than many kin, it draws moisture from the air if left exposed. Careful packaging and short-term refrigerated storage go a long way toward preserving quality. Lab teams often rely on moisture-proof containers with simple desiccant packs to extend shelf life and prevent caking.
Another point is the occasional bottleneck in supply, especially during periods of high demand tied to patent race periods or seasonal spikes in agrochemical research. Long-time buyers know the practicalities here: It pays to establish relationships with reputable suppliers and maintain a buffer stock for sudden project changes. Larger-scale syntheses sometimes mean negotiating batch reservations well in advance.
Technological advances may open doors to greener production methods in the near future. Traditional synthesis routes to 2-Cyano-5-Hydroxypyridine rely on cyanation and selective pyridine functionalization, which involve handling hazardous reagents and generate waste. Some researchers push for milder processes, like flow chemistry techniques or bio-inspired catalysis, which could drop hazardous byproducts and lower energy needs. Early pilot data from academic labs hint at real progress in this area, reflecting broader trends toward sustainable manufacturing.
Standard lab safety habits apply here as with any pure organic intermediate. Gloves, goggles, and appropriate fume extraction keep the process straightforward. Personnel training is critical, especially for junior chemists who might not yet spot subtle hazards associated with handling nitriles or phenolic groups. Careful weighing and transfer—using non-glass spatulas—can save time spent cleaning broken glass or accidentally contaminating a whole bottle.
Every chemist who has spent time with specialty aldehydes or structurally close intermediates knows that accidents don’t always stem from major spills. Little things, like residual dust on benchtops or careless resealing after use, can introduce both health and cross-contamination risks. Teams adopting a culture of tidy surfaces and clear labelling tend to avoid the issues that slow projects or even derail product integrity.
Waste disposal tracks with prevailing hazards for nitrile- and hydroxy-containing organics: segregated bins, no dumping down the drain, and regular oversight for compliance. Building this knowledge and vigilance into team routines pays off both in safety and in research efficiency. There’s a certain reassurance in knowing exactly what you’re handling, and 2-Cyano-5-Hydroxypyridine comes with enough literature data and community experience to prevent surprises.
Few things drive chemistry forward like open exchange and shared learning. Organizations committed to transparency and knowledge sharing help new entrants adopt meaningful best practices. Many senior chemists keep informal logs, sometimes just scribbled notes on reaction margins, which create a kind of living playbook for successfully deploying intermediates like 2-Cyano-5-Hydroxypyridine. Passing along these notes—either through formal SOPs or as informal mentorship—helps maintain standards even as techniques and technologies shift.
Greater outreach between supplier quality control teams and end-users has prompted improvements in packaging, lot tracking, and even technical documentation. Modern suppliers who engage in dialogue with their user base can anticipate shifts in demand and preempt issues before they reach the lab. Feedback loops between chemists and suppliers have led, in some cases, to improved handling, documentation, and purity options.
On the technical front, the next few years look promising for smarter synthesis routes and greener protocols. As more chemists adopt continuous-flow or enzyme-inspired methods, the expectation is that processes once limited to high-cost or high-waste operations will become more efficient and approachable. This shift won’t only benefit the bottom line or environmental reports—it stands to fuel a new range of applications, from custom pharmaceuticals to advanced agrochemicals and beyond.
Having reliable reagents on the bench is central to ambitious lab work. 2-Cyano-5-Hydroxypyridine doesn’t just fill a gap somewhere between generic building block and specialty item—it actively shapes the workflows of research teams committed to discovery. Years of published data and hands-on experience give chemists the confidence to pursue challenging syntheses that would otherwise demand complex workarounds or riskier intermediates.
The compound’s appeal lies in the details: straightforward reactivity, straightforward handling, and documentation that stands up to scrutiny. Trust comes not only from technical specs but the experience of getting through a campaign with fewer headaches and surprises. Researchers who lean on this reliable intermediate often find their work moves forward just that little bit smoother, thanks to choices made long before the reaction flask gets clamped and the heating mantle switched on.
Looking to the future, there’s no shortage of opportunity for further optimization and collaborative progress. By supporting transparency, smarter supply chains, and greener chemistry, everyone who depends on these essential molecules contributes to a cycle of improvement that benefits the field at large. In the end, it’s the combination of preparedness, community wisdom, and steady hands that keep research rolling—and 2-Cyano-5-Hydroxypyridine has earned its spot as a quiet, dependable partner in that ongoing story.