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HS Code |
765499 |
| Iupac Name | 4,6-dichloro-3H-imidazo[4,5-c]pyridine |
| Cas Number | 162011-90-7 |
| Molecular Formula | C6H3Cl2N3 |
| Molecular Weight | 188.02 |
| Appearance | White to off-white solid |
| Melting Point | 218-222°C |
| Solubility In Water | Slightly soluble |
| Smiles | Clc1nc2ncc(Cl)nc2n1 |
| Inchi | InChI=1S/C6H3Cl2N3/c7-3-1-4-5(8)10-2-9-6(4)11-3/h1-2H,(H,9,10,11) |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 4,6-dichloro-3H-imidazo[4,5-c]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 25 grams of 4,6-dichloro-3H-imidazo[4,5-c]pyridine, labeled with hazard warnings and batch information. |
| Container Loading (20′ FCL) | 20′ FCL container holds 12 MT of 4,6-dichloro-3H-imidazo[4,5-c]pyridine, packed in 25 kg fiber drums, palletized. |
| Shipping | 4,6-Dichloro-3H-imidazo[4,5-c]pyridine is shipped in tightly sealed containers, protected from light and moisture. It is transported as a non-hazardous chemical, compliant with local and international regulations. Adequate labeling and documentation are provided, and the package is handled with care to prevent spillage or contamination during transit. |
| Storage | 4,6-Dichloro-3H-imidazo[4,5-c]pyridine should be stored in a tightly sealed container at room temperature, in a cool, dry, well-ventilated area away from sources of moisture, heat, and incompatible substances. Protect it from light and direct sunlight. Ensure appropriate labeling and keep away from strong oxidizing agents. Store in accordance with local safety regulations and guidelines for hazardous chemicals. |
| Shelf Life | 4,6-Dichloro-3H-imidazo[4,5-c]pyridine is typically stable for at least two years when stored cool and dry, protected from light. |
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Purity 98%: 4,6-dichloro-3H-imidazo[4,5-c]pyridine with purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Melting Point 210°C: 4,6-dichloro-3H-imidazo[4,5-c]pyridine with melting point of 210°C is used in high-temperature organic reactions, where it provides thermal stability during process scaling. Molecular Weight 204.01 g/mol: 4,6-dichloro-3H-imidazo[4,5-c]pyridine with molecular weight of 204.01 g/mol is used in medicinal chemistry research, where accurate dosing and molecular calculations are required. Particle Size <20 μm: 4,6-dichloro-3H-imidazo[4,5-c]pyridine with particle size less than 20 μm is used in formulation of solid dispersions, where it promotes uniform mixing and improved solubility. Stability Temperature up to 150°C: 4,6-dichloro-3H-imidazo[4,5-c]pyridine with stability temperature up to 150°C is used in chemical process development, where it maintains structural integrity under reaction conditions. |
Competitive 4,6-dichloro-3H-imidazo[4,5-c]pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Producing 4,6-dichloro-3H-imidazo[4,5-c]pyridine day-in and day-out, the team on our lines understands that stable supply and consistent quality are more than boxes to tick—each batch tells a story. The industry likes big names, but under the microscope, this heterocycle does a tough, specialized job that generic intermediates or off-the-shelf chlorinated imidazoles leave unfinished. We know. We’ve compared results from pilot runs and scale-ups, and the feedback from our customers in pharmaceuticals and fine chemical development continues to highlight the unique synthetic advantages of this compound.
4,6-dichloro-3H-imidazo[4,5-c]pyridine, by its molecular structure, stands out for those building diverse scaffolds in the pharmaceutical world. It’s a relatively rigid blueprint: introducing both reactivity and selectivity through its dichloro pattern, which influences the way downstream groups attach. We’ve watched R&D teams struggle with positional issues on regular imidazopyridines, where substitution occurs less cleanly or stalls, leading to unproductive runs and higher purification costs. With our product, yields rise and rework drops, because the 4,6-dichloro positions have been time-tested for controlled reactivity.
In-house, producing this compound isn’t a matter of running an old formula on autopilot. This material demands careful chlorination steps and tight control of reaction parameters. We’ve upgraded several points in our synthesis to minimize byproducts, eliminate metal contaminants, and improve particle handling. Peers in the industry sometimes cut corners, resulting in off-white material or product that gunks up equipment. We avoid these pitfalls by running a fluid operation and maintaining a sharp focus during isolation and drying. Every drum and flask must leave our floor clean and consistent, because setbacks on the customer’s end are our concern as well.
Chemists who’ve handled unstable intermediates or moisture-sensitive halogenated compounds know the headaches of caked samples, false readings, or material that drifts away from stated specs. We focus on purity. Most of our regular clients request at least 98% by HPLC analysis, and our process consistently shoulders that mark batch after batch. The color remains crisp—no brownish tinge to cause second-guessing. Handling is straightforward: low-moderate hygroscopicity means it keeps well in doubled-sealed containers under ambient storage.
Some buyers on the international stage chase a lower price from blending houses who offer mixed-grade or recycled material. Our line doesn’t approach the product this way: our customers expect uniform granulation and controlled particle size, and we deliver on those terms because decades of scaling experience have taught us the cost of callbacks. Material that’s improperly dried, or packed with trace solvents, stalls downstream. We analyze every delivery for residual solvents and halide levels, minimizing the guesswork for buyers scaling up synthesis for new pharmacophores or crop protection compounds.
In pharmaceutical R&D, medicinal chemists look to 4,6-dichloro-3H-imidazo[4,5-c]pyridine as a smart starter for both exploratory library generation and advanced lead optimization. The dichloro configuration enables selective coupling reactions—Suzuki, Buchwald-Hartwig—without unduly activating the entire ring. Over the years, we have seen the marketed kinase inhibitor portfolios grow from early leads bearing just one imidazopyridine motif. Our compound features prominently in patents for ATP-competitive molecules and small-molecule enzyme regulators. Chemical teams in Asia, Europe, and the US reach for it when designing families of analogs because switching out the chlorine atoms can dramatically adjust selectivity and potency profiles.
From our production notes and feedback, formulation scientists also choose this compound for developing agricultural actives that need weathering resistance and systemic activity. The dual-chloro substitution helps resist metabolic degradation in the field, which competing building blocks often fail to offer, resulting in poor product longevity. Our material holds up in pre-formulation stress tests, creating less work for downstream teams.
We hear from chemists who have tried other halogenated imidazopyridines or even made in-lab variations just to cut lead times. While some claim cost savings or slightly easier access, the reality on scale proves less convenient. 2,6-dichloro or 2,4-dichlorinated compounds often react at the “wrong” positions, producing mixtures that require extra column runs or complex purification. Other analogs supply only a single reactive site, limiting the ability to dial in variation at both ends of the molecule. When pharmaceutical teams chase robustness and functional flexibility, our dichloro version proves itself in the lab and in the kilo plant.
Substituted imidazopyridines that lack both halides or introduce alternative groups at those positions can show instability, especially when exposed to process conditions involving bases, acids, or high heat. Researchers report side reactions that scuttle entire campaigns. In contrast, our product’s bench stability has been proven over long hauls—multiple heating and storage cycles, withstanding moisture during scale-up and transit.
Unlike trade houses who repackage unknown sources, we keep full lineage from batch ingredients to drum shipment, and our operators stand behind every step. We source high-purity starting materials, and our process documentation includes full traceability, so any customer can review analytical data not only for current batches but for runs from years past. Facility audits don’t pressure us; they make us improve. Years of familiar faces at customer facilities means each audit simply encourages us to maintain clean practice and honest documentation.
Every chemical facility faces new environmental scrutiny and regulations. We own the responsibility by minimizing chlorinated solvent use, recycling where possible, and continuously updating washing and extraction steps to carve away byproduct waste. The team has piloted changes that cut energy use during drying, with results reflected in lower emissions figures year over year. Where competitive operations rely on outdated venting standards, we opt for modern scrubber technologies. Nobody in the downstream supply chain appreciates blowback from poorly managed production, so we take pride in leaving less burden in our wake.
We’ve had chemists bring us side-by-side samples pulled from major distributors around the world. After running identical coupling, halogen exchange, or cyclization reactions, the outcome sits in the books: fewer side products, crisper NMR, and higher isolated yields from our material. Clients tell us directly—one recent contract lab found that their reaction failure rates with a competitor’s product more than doubled, once labeled product purity fell below 97%, and carried higher heavy metal traces.
The price premium for a dependable grade pays for itself in time saved and headaches avoided, especially when working under tight patent deadlines or government compliance reviews. That’s not sales talk; anyone who has ever rerun a multiphase process over a matter of five or six percent purity loss knows the cost in solvents, time, and stress.
In years of running mid-tonnage lots, we’ve seen how much damage happens during global transit—moisture, accidental warming, and rough handling. Our ops team moved early to double-jar every shipment, include humidity guards, and tight-pack drums so that powder flow remains stable even after long voyages. Distributors sometimes cut corners and rebag or re-drum in uncontrolled ambient air. The headaches created by this practice show up weeks or months later, as ‘stale’ product comes back or sits too long on a shelf. Direct-from-manufacturer supply straightens the path, and we’ve built enough redundancies to handle the anomalies that still crop up.
More than once, returning customers have cited unanticipated stability from our packaging and post-production handling. The difference comes down to firsthand knowledge—storing this type of material isn’t quite like housing bulk acids or simple chlorinated intermediates. It demands care for both product and the teams on the handling end.
Regulatory documentation for active intermediates can become a minefield, as different regions (Europe, US, Japan, and several emerging markets) request varying levels of analytical detail and traceability. Over the span of multiple market cycles, we have developed a responsive approach, gathering proper documentation from the earliest synthetic stages through finished lot testing and shipping. When regulatory bodies ask for full impurity profiles or periodic sample retention, we answer not with generic documentation but with targeted data reflecting reproducibility and real-world analytical results.
Our track record includes smooth passage for our material in both small-scale research applications and large-scale cGMP manufacturing audits. This does not come through blanket testing but by customizing analytics to each request, whether through high-throughput LCMS, residual solvent analysis, or tailored stability testing based on the intended use case. The goal is not simply ticking regulatory boxes, but actually easing the way for end users to work with governing agencies and move their projects forward without red tape delays.
Anybody tracking global supply lines over the last decade remembers how fast a single upstream incident can ripple through the entire finished product timeline. We’ve run into everything from port shutdowns, to force majeure at chlorinating agents, to abrupt regulation changes on raw material imports. Our answer comes from experience rather than sales spin: diversify trusted backup suppliers, maintain inventory buffers, and keep lines of direct customer communication wide open. One recent incident saw worldwide prices spike as a major Asian supplier of key halogenating agents diverted feedstock. Because our sourcing teams built redundancy, our customers received their quota while others waited indefinite periods.
No system is invincible, but keeping multiple feet on the ground across sourcing, workflow, and logistics remains the most honest buffer against tomorrow’s crisis.
A few practical tips bear repeating. Chemists developing new APIs or formulations: ask for all available analytical data upfront. If the packaging or documentation looks generic, probe deeper—materials handled in uncontrolled environments may pass short-term checks but create costly issues downstream. Stop using mixed-batch samples from unknown origins when beginning scale-up or regulatory processes. Investment here saves so much more than it costs.
R&D labs sometimes try to cut initial development costs by using leftover lots or research-grade stocks when scaling for preclinical batches. Years of experience show that shifting to production-grade 4,6-dichloro-3H-imidazo[4,5-c]pyridine early in the process prevents headaches when shifting up to cGMP or passing verification by external inspectors. It’s tempting to get “good enough” for process chemistry, but the risk is false confidence in results, only to run into batch rejection later. Consistency matters most during the critical handoff from bench to pilot plant.
We never claimed that our synthesis runs represent the ceiling of what’s possible. Every year, our R&D staff evaluates green chemistry advances, aiming for both better process efficiency and lower lifecycle environmental impact. Waste stream minimization and energy footprint recalibration remain standing projects. Whenever clients have special requests—be it a new crystal form, a higher-purity variant for regulated markets, or integrated validation for a new compliance target—we treat it as a process challenge worth solving, not a box to check.
Continuous research sometimes leads us to trial new catalysts or greener solvents; those findings roll directly into production only after full validation, because rushing to untested technology can cause bigger problems than it solves. Our long-standing relationships with technology partners and specialized equipment machinists push the product forward, improving both yield and reliability for end users.
The credibility of 4,6-dichloro-3H-imidazo[4,5-c]pyridine as a reliable intermediate sits not in abstract properties or shelf descriptions but in the hard lessons of real-world handling, long-term stability, and clean run analytics at scale. We have staked our reputation on putting only what we have produced, vetted, and released directly into the hands of chemists and formula teams. We stand behind every gram, aware that the genuine test lies well after the invoice clears and the barrels are opened in labs halfway around the world. Trust takes more than meeting a spec; it takes consistent attention from synthesis to shipping to shelf, honed by years of feedback and knowledge built on the factory floor.