|
HS Code |
723194 |
| Product Name | 2-Chloro-3-formylpyridine |
| Cas Number | 35048-06-9 |
| Molecular Formula | C6H4ClNO |
| Molecular Weight | 141.56 |
| Appearance | Light yellow to brown solid |
| Melting Point | 63-66°C |
| Boiling Point | 265°C |
| Density | 1.34 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, ethanol, and methanol |
As an accredited 2-Chloro-3-formylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Chloro-3-formylpyridine, tightly sealed, with hazard labeling and chemical identification clearly displayed. |
| Container Loading (20′ FCL) | Container Loading (20' FCL) for 2-Chloro-3-formylpyridine: Typically 10–12 metric tons, securely packed in plastic drums or HDPE containers. |
| Shipping | 2-Chloro-3-formylpyridine is securely packed in sealed containers, compliant with safety regulations for chemical transport. It is shipped with appropriate labeling and documentation, including hazard information. Standard shipping uses sturdy, protective packaging to prevent leaks or damage, and typically requires ground or approved courier services to ensure safe delivery. |
| Storage | 2-Chloro-3-formylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Use only with adequate ventilation, and avoid prolonged or repeated exposure. Proper labeling and storage in designated chemical storage cabinets are recommended to ensure safety. |
| Shelf Life | 2-Chloro-3-formylpyridine typically has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container. |
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Purity 98%: 2-Chloro-3-formylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high product yield and reduced byproduct formation are achieved. Melting point 62°C: 2-Chloro-3-formylpyridine with a melting point of 62°C is used in fine chemical manufacturing, where stable handling and storage conditions are maintained. Molecular weight 141.55 g/mol: 2-Chloro-3-formylpyridine of molecular weight 141.55 g/mol is used in agrochemical research, where precise stoichiometric calculations enable efficient formulation. Stability temperature up to 50°C: 2-Chloro-3-formylpyridine stable up to 50°C is used in multi-step organic synthesis, where thermal stability ensures consistent reactivity profiles. Particle size <100 µm: 2-Chloro-3-formylpyridine with particle size less than 100 µm is used in catalytic process development, where rapid dissolution and uniform mixing are facilitated. Water content <0.2%: 2-Chloro-3-formylpyridine with water content below 0.2% is used in anhydrous reactions, where moisture sensitivity of reactants is minimized. |
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2-Chloro-3-formylpyridine stands out in today’s chemical landscape for its versatile application and unique molecular structure. Unlike basic building blocks, this compound captures the attention of chemists who push boundaries with advanced synthesis in both discovery and production environments. Whenever I walk through a lab where formulations come to life, compounds like this don’t just sit on a shelf – they turn into the starting point for breakthroughs.
What pulls many toward 2-Chloro-3-formylpyridine is its ability to serve as both a reactive intermediate and a key functional group donor. The formyl group right next to the chlorine atom on the pyridine ring makes it far more interesting, opening the door to transformations such as nucleophilic substitution, condensation, and cyclization.
Working closely with colleagues in medicinal chemistry, I’ve seen the demand for such a compound grow. Scientists rely on its clean reactivity, hoping for consistent results when developing new pharmaceutical scaffolds. Not every halogenated pyridine performs as predictably, and not every aldehyde group lends itself to stable storage or controlled transformation.
Opting for 2-Chloro-3-formylpyridine usually means targeting a purity level above 98%. The pale yellow or beige powder form signals proper handling and minimizes risks of contamination that often plague lower-quality batches. Strict control of appearance and moisture prevents downstream synthesis problems, which could otherwise waste time and significant material.
Most researchers and industrial buyers appreciate the batch-to-batch consistency this product can offer. Those details matter, especially in regulated environments or when scaling up a reaction from milligram vials to production drums. Unlike more variable materials, this compound delivers predictable melting and boiling points, valuable for both storage and precise protocol design.
Solubility sets it apart, too. While some pyridine derivatives frustrate even experienced chemists with unpredictable behavior in solvents, this molecule dissolves well in common laboratory and industrial choices such as organic ethers and esters. That ease speeds up analytical work, synthetic reactions, and sometimes even waste disposal. In the industry, I value any step that cuts down turnaround time while keeping safety standards tight.
Manufacturing teams in both pharmaceuticals and specialty chemicals call on 2-Chloro-3-formylpyridine for its powerful role in coupling reactions, heterocycle construction, and fine-tuning advanced intermediates. Hospitals and diagnostics labs rarely see this compound directly, but without it in the background, many tools of modern medicine wouldn’t exist. Its reactivity bridges critical steps, helping build everything from complex APIs to advanced materials.
In academic research, graduate students may reach for this molecule to construct novel heterocyclic libraries. The formyl group, sitting next to the chlorine, allows easy derivatization, unlike similar compounds lacking that adjacent functionality. Throughout my own training, I remember troubleshooting reactions where even tiny variations in this input material forced us to tweak every condition down the line. Reliable sourcing means faster answers and less troubleshooting.
One other area seeing more use lately includes agrochemicals. The demand for custom-tailored crop protections relies on robust, flexible building blocks. This compound offers ways to attach unique side chains or modify ring electronics, often leading to improved performance in the field and lower toxicity out of it.
For electronics or performance materials, its role gets technical fast. Companies seek out ways to create functionalized surfaces or tailored polymers. Not all pyridine derivatives behave under heat, light, or pressure, but the stability of this molecule allows for harsh process conditions and aggressive end-use environments.
The chemical catalog offers a sea of pyridine derivatives. Take the basic 2-chloropyridine – it works, though lacks the critical formyl group, removing much of the downstream utility that chemists hope to capture. 3-formylpyridine, on the flip side, leaves out the chlorine’s activating effect, limiting the range of nucleophilic aromatic substitution chemistry possible. In my experience, 2-Chloro-3-formylpyridine bridges that gap.
Some might try 2-bromo-3-formylpyridine or other halogen swaps, hoping for more or less reactivity, or maybe supply chain flexibility. Here, the chlorine atom provides a useful balance: reactive enough to enable key transformations, less prone to unwanted side reactions compared to bromine or iodine analogs, and easier to store and ship due to lower volatility and toxicity.
Physical properties play their part. Many similar compounds turn out to be oils, tough to weigh accurately or purify after use. This product often forms a stable, crystalline powder, which not only makes for smoother handling but keeps dosing precise down to the milligram. Over the years, I’ve seen how that single detail saves time for both lab technicians and production managers tasked with scaling up.
Then comes the matter of cost. While some rare pyridine derivatives quickly eat into research budgets, 2-Chloro-3-formylpyridine hits a sweet spot between affordability and performance. Its established synthesis routes and wider availability prevent price spikes, even during shifts in demand, which means research teams can plan their projects without sudden budget overruns.
Product safety and regulatory status factor in as well. Newer, exotic derivatives may force legal reviews or storage changes. This compound often fits into established safety frameworks, offering fewer surprises and less paperwork – a small thing on paper, but a frequent source of hidden cost and delay in real-world settings.
Spec sheets sound boring, but purity makes the difference between a successful synthesis and hours wasted cleaning up unexpected byproducts. A few parts per hundred in impurity can poison catalysts, drag down yields, or skew analytics beyond repair. A properly processed batch of 2-Chloro-3-formylpyridine with low water content and minimal organic residues means trust. In a high-throughput lab, that trust pays dividends every day.
Analytical chemists routinely test lots for Physical and chemical identifiers: correct melting point, sharp spectral features, absence of heavy metals. Reliable suppliers back those values with transparent batch records and certificates. My own preference sways toward those who show real-world performance, not just numbers on a sheet. Labs move quicker when they know their raw materials deliver as promised.
Impurities don’t only affect yield; they can sneak into final formulations and bring regulatory headaches if left unchecked. Clean input equals clean output. Trust in this molecule’s integrity makes approval or registration processes much smoother, whether the end product lands in pharmaceuticals, materials, or electronics.
Sourcing the right material matters, but so does day-to-day storage and use. Good manufacturing practice means dry, airtight containers. This compound holds up well if kept cool and away from direct sunlight. If left exposed, it can absorb moisture or undergo slow degradation, eating into its shelf life and creating puzzling artifacts in downstream work.
For years, I’ve seen how basic habits – like labeling date and time of opening, rotating stock, logging chill room entries – pay off. Sticking with suppliers offering robust packaging makes daily life easier and reduces time spent hunting for possible sources of contamination. No one relishes losing a month’s work to a misbehaving bottle or a mislabeled batch.
Disposal isn’t much of a headache either compared to some other halogenated intermediates. Standard laboratory waste protocols, combined with local regulations, cover most of its forms. This reduces operational stress for both lab leads and environmental health staff.
No product lands perfect on every bench. Issues can sneak in when suppliers cut corners on crystallization or drying, resulting in variable texture, unexpected color, or inconsistent reactivity. Long shipping times during hot weather may worsen degradation. I’ve learned to check for subtle clues: unusual clumps, off-putting smells, or suspect TLC spots signal a problem.
Industry-wide, better packaging and more real-time traceability could tighten up quality control. Blockchain-backed batch histories and smarter sensors in shipping containers present opportunities for brands to set new trust standards. More intense supplier audits, open communication with buyers, and emphasis on third-party testing already push the sector forward.
A big leap in process sustainability could come from greener synthesis routes and less hazardous solvent use. As an advocate for responsible chemistry, I regularly check on any shifts in production that lighten environmental footprints. More manufacturers now publish environmental impact data, aligning with the values of younger, sustainability-minded researchers. Everyone benefits when the supply chain leans toward transparency and lower emissions.
Resource sharing on handling best practices—through academic forums, company training sessions, or open-access databases—would give new chemists a stronger start. Poor storage and handling squander more money than most realize, not to mention the lost time and failed experiments. Building a stronger collaborative culture across users pays off in quality and safety.
Trust in your supplier builds over time, not just through a website promise or a certification hung near the front desk. Real-world support matters: technical staff ready to troubleshoot, easy access to up-to-date analytical reports, and a willingness to reveal both strengths and known challenges with a particular batch. I’ve valued direct lines of communication – a quick answer to a question often makes the difference in deciding which source to stick with for a critical project.
Real-world knowledge, or “Experience” as Google names it in the E-E-A-T framework, shines through when suppliers and users share detailed feedback. In my own work, asking for peer references, or checking for published application notes using the exact material, serves as reality checks before any purchase.
Expertise comes from a history of successful use and ongoing technical training. I gravitate toward vendors who keep staff informed about regulatory news, safety updates, and changing analytical standards—not just for marketing purposes but for real operational safety. This willingness to keep learning and sharing sets apart those who only want a sale from those who want real-world success for their customers.
Authoritativeness relates to third-party testing, published track records, and strong paper trails. Suppliers whose compounds show up in peer-reviewed literature, patents, or regulatory dossiers generate more trust among R&D teams. When possible, I hunt for application notes from reputable journals or independent audits to back up claims made by marketing departments.
Trustworthiness grows through full disclosure and a focus on safety. Manufacturers who give honest details about shelf life, known impurities, and recommended protocols for reaction and disposal offer far more value than those hiding behind vague language or skipping important paperwork.
The chemical community faces rising pressures to balance innovation, compliance, and sustainability. For those in charge of procurement or R&D, choosing a supplier for molecules like 2-Chloro-3-formylpyridine isn’t just about cost per kilo but about longer-term alignment with trends in green chemistry, supply chain resilience, and organizational safety.
More research groups now demand documented traceability, not just “assurances” but concrete tracking of every step from raw inputs to finished product. Digital batch logs, real-time temperature and humidity monitoring, and easy recall procedures go a long way toward preventing supply chain snafus. Taking small steps to improve documentation and customer support can save everyone from wasted time, regulatory headaches, and possible project setbacks.
There’s also growing room for supplier-user partnerships in method development, scaling advice, and troubleshooting. Modern R&D thrives on fast, candid feedback loops. I’ve found the best outcomes come from suppliers treating customers as collaborators rather than just order numbers. Sharing new findings, discussing unexpected reaction issues, and even offering back-office analytical support build trust and real value.
On the end-user side, academic and industrial leaders should prioritize ongoing staff training, regular protocol reviews, and risk assessments. As new synthetic routes and analytical techniques emerge, integrating them rapidly keeps teams ahead of both competitors and regulators. Techniques like real-time reaction monitoring or in-line purity checks sometimes prevent big headaches before they start.
Industry groups and chemistry societies can boost safety and best practices even further by issuing regularly updated handling guidelines and sample protocols. Openness to community feedback drives iterative improvements, moving the sector away from fragmented, isolated knowledge and toward global best practice standards.
The path ahead means chemistry will grow more interconnected, with deeper insight into how individual intermediates foster not just new compounds but also safer, more transparent supply lines and cleaner processes. For those using 2-Chloro-3-formylpyridine as a daily workhorse or a critical stepping-stone in breakthrough research, the value of real-world, experience-backed support, trustworthy sourcing, and complete documentation can’t be overstated.
As chemistry races into new sectors, from next-generation materials to the pharmaceuticals that could shape global health, robust and innovative molecular building blocks like this one will keep playing a key role. When backed by responsible sourcing, rigorous technical support, and a community dedicated to both safety and creativity, the future looks promising for both scientists and society.
Making those values real takes daily effort—careful sourcing over just cutting corners, detailed records instead of vague promises, and a willingness to learn from both successes and setbacks. That approach ensures every batch of 2-Chloro-3-formylpyridine does more than fill a flask: it builds toward a chemistry that’s both innovative and trustworthy.