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HS Code |
338323 |
| Name | 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine |
| Chemical Formula | C7H3Cl2N3 |
| Cas Number | 120945-08-0 |
| Appearance | White to off-white solid |
| Melting Point | 176-180 °C |
| Solubility In Water | Insoluble |
| Smiles | Clc1cc2nccc(n2c1)Cl |
| Inchi | InChI=1S/C7H3Cl2N3/c8-4-1-5-6(9)3-10-7(12-5)11-2-4/h1-3H,(H,10,11,12) |
| Pubchem Cid | 145056 |
As an accredited 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 10-gram amber glass bottle sealed with a tamper-evident cap, labeled with product name, CAS number, and hazard precautions. |
| Container Loading (20′ FCL) | 20′ FCL: Packed in 25kg fiber drums, secured on pallets; total load approx. 8–10 MT, ensuring safe chemical transport. |
| Shipping | 4,6-Dichloro-1H-pyrrolo[3,2-c]pyridine is shipped in tightly sealed containers to prevent moisture and air exposure. It is packaged according to regulations for hazardous chemicals, with appropriate labeling and documentation. Transportation is carried out by certified carriers to ensure safety and compliance with all relevant chemical shipping standards. |
| Storage | 4,6-Dichloro-1H-pyrrolo[3,2-c]pyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area away from sources of ignition, strong oxidizers, and incompatible materials. Ensure the storage area is equipped for handling hazardous chemicals and clearly labeled. Use appropriate personal protective equipment (PPE) when handling. |
| Shelf Life | Shelf life of **4,6-dichloro-1H-pyrrolo[3,2-c]pyridine**: Stable for 2 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal reaction yields. Melting Point 110°C: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with a melting point of 110°C is used in organic electronics manufacturing, where controlled solidification enhances device fabrication consistency. Particle Size ≤50 µm: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with particle size ≤50 µm is used in fine chemical formulation, where fine dispersion improves product homogeneity. Stability Temperature 80°C: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with stability temperature 80°C is used in high-temperature catalysis research, where thermal stability enables reliable screening tests. Water Content <0.2%: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with water content <0.2% is used in moisture-sensitive synthesis processes, where low water levels prevent side reactions. Assay ≥99%: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with assay ≥99% is used in medicinal chemistry R&D, where high assay value supports reproducible analytical results. Molecular Weight 200.02 g/mol: 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine with molecular weight 200.02 g/mol is used in structure-activity relationship studies, where defined molecular mass facilitates accurate bioactivity modeling. |
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Walking through our production floor, every batch of 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine carries a story of strict process discipline and practical problem-solving. This compound isn’t just another entry on a spreadsheet. It comes from years of tweaking, piloting, and adjusting our controls to serve chemists and manufacturers balancing both creativity and deadlines. Anyone who handles heterocyclic building blocks for drug discovery or advanced materials has likely crossed paths with one of the many pyrrolopyridine compounds. Yet, adding two chlorine atoms at the 4 and 6 positions in this molecule opens distinct doors in synthetic chemistry, leading to derivatives that fuel some of the most interesting work in pharmaceuticals and specialty chemicals.
On paper, 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine looks deceptively simple: a bicyclic system, chlorinated where it makes synthetic sense. What stands behind that simplicity involves the real challenges of scale-up—consistent reactivity, elimination of side reactions, drying without caking, and reliable shelf-life. Every time we run a batch, we’re not just aiming for a passing GC result. Our eyes are on long-term stability under realistic storage conditions and on ensuring that chemists receive a clean, crystalline material that dissolves and reacts as expected. Customers in Europe, North America, and Asia have different preferences and expectations, but the fundamentals stay the same: repeatable purity, batch-to-batch homogeneity, and an honest dialogue about trace impurities.
We keep synthesis under well-controlled temperatures and inert conditions to lock in purity levels, typically delivering material above 98%. But high assay alone isn’t the end goal. We track isomeric and halogenated byproducts by HPLC and LC-MS, then push out-of-spec byproducts below application-relevant limits. Each lot passes water content testing; moisture alters handling for many users, so Karl Fischer titration isn't optional. For some customers, residual metals from catalyst systems matter; we tune washing and recrystallization steps so palladium, copper, and related impurities fall below tough pharmaceutical project cut-offs. These priorities, born out of day-to-day plant realities and feedback from laboratories, drive how we run our plant more than any certificate template ever could.
Sourcing 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine from a manufacturer means working with a product that often sets the stage for Suzuki, Buchwald-Hartwig, and other complex couplings. Purity and isomeric cleanliness keep the synthetic routes in research departments moving—side products or wrong regioisomers in the starting material can derail expensive screening campaigns. The unique substitution pattern in our material stands apart from 2,3-dichloro or 5,7-dichloro analogs, which behave differently in substitution and cross-coupling protocols due to both steric environment and electronic influence on the ring. This is not mere trivia for the process chemist who needs scale—4,6-dichloro sees routine use where orthogonal functionalization matters: one chlorine can be swapped selectively while the other remains inert, giving experienced chemists more leeway in building up complexity with fewer protecting group headaches.
In practice, this molecule slips directly into the modern medicinal chemist’s playbook, especially for programs targeting kinase inhibitors and CNS therapeutics. Its scaffold, with precisely positioned chlorines, delivers a balanced mix of reactivity and metabolic resilience in potential drug candidates. For those working beyond pharma, the same core structure helps design novel optoelectronic materials and specialty pigments where electron density and substitution pattern affect photophysical properties.
Years of refining our process have taught us the difference between meeting a spec sheet and anticipating the real-life questions from a research chemist. We confirm the melting point and single-crystal data for structure confirmation, but there’s more under the hood. Sharp melting point ranges mean something here—a sign that purification worked, not just a checkbox for the quality team. Assay by HPLC or GC is always measured against validated standards, and spectra are cross-checked by NMR. Sometimes, a customer's method flags a ghost impurity our in-house methods miss. Those phone calls spur further improvements, often leading to even tighter in-process controls.
We don't ship based solely on a purity number. We check particle size distribution, especially for scale-up users who care about dusting or filtration times. Moisture content and solubility profiles matter because they impact downstream coupling yields. Creators of preclinical compounds and scale-up teams both need material that behaves predictably, whether wetted with DMF or dried for weighing under argon. That predictability doesn't happen without hands-on vigilance in storage, packing, and logistics.
Over the years, our 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine has shown up in some ambitious programs worldwide. We’ll never see the headlines for scientific breakthroughs, but we know our work feeds into projects developing next-generation kinase inhibitors, antifungal agents, and new electronic building blocks. In early-stage drug discovery, this building block helps medicinal chemists test SAR hypotheses by enabling fast diversification through cross-coupling or nucleophilic aromatic substitution. For process chemists developing scaleable syntheses, the reliable availability and purity mean fewer false positives and less wasted time in downstream purification.
One research partner leveraged our product to build a library of pyrrolopyridine derivatives, eventually leading to scalable routes for a clinical candidate—only possible because each delivery matched the last in performance. For those working on heteroaromatic dyes for industrial applications, electronic structure and chemical reactivity require absolute confidence in batch composition; otherwise, downstream properties drift, leading to waste and costly reformulation. We’ve seen both sides of this challenge and devote real resources to minimizing these risks.
Scaling 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine from milligrams to multi-kilogram lots wasn’t a walk in the park. The reaction sequence demands selective chlorination and effective control of byproduct formation. Chlorine introduction must avoid side-chain halogenation and ring over-chlorination, which both complicate isolation and purification. Our team invested time in catalyst screening, solved liquid–liquid phase challenges, and implemented real-time monitoring to catch side reaction spikes before material losses mount.
Batch records capture every tweak, and plant operators flag deviations right at the moment rather than after-the-fact, preserving integrity and reducing rework. We take pride in how we closed the gap between high-yield literature methods and the actual, rugged conditions of process-scale reactors—mixing times, temperature ramps, and solvent swaps that make the difference between a clean product and a sticky, low-assay mess. Not every process step scales linearly. Learning from leaks, equipment fouling, and filter blockages taught us to build a safer, more efficient sequence.
Another key piece: controlling odor and minimizing chlorinated effluent. As a responsible manufacturer, we upgraded our capture system for vent gases and implemented multi-stage distillation to recover and recycle solvents wherever feasible. Environmental controls are not just about compliance; reducing emissions, even below regulated thresholds, shows our commitment to the communities we work in and the people who manufacture the product every day.
Every lot bears a unique record, but it’s what happens after delivery that matters just as much. We keep two-way lines open with users, tracking complaints or surprises back to root causes. If a customer’s analytic team uncovers a new impurity, our lab investigates at scale, not just at bench. Even a minor source of batch-to-batch variation can show up as a real-world headache when scaling up to pilot-plant chemistry. We keep archived retain samples, enabling retrospective checks when formulation shifts arise months after delivery.
These lessons accumulate and shape our future batches. Integrating feedback means more than issuing corrections; we dive into upstream raw material quality, adjust partner certifications, and, if necessary, revisit our hazard assessments to ensure not only a consistent product but safer operations. Transparent labeling, adequate shelf-life assignment, and responsible shipment tracking come from this ongoing dialogue, giving buyers concrete information instead of marketing gloss.
Among the family of halogenated pyrrolopyridines, each substitution pattern serves a different need. Our 4,6-dichloro product distinguishes itself with its regioselective reactivity—an asset for sequence-specific coupling or for controlled dehalogenation. Chemists familiar with 3,5-dichloro or non-chlorinated core structures have noted differences in coupling yields and side-product spectra. This means our product streamlines workups and simplifies planning, offering a more reliable platform for late-stage derivatization and custom fluorophore design.
As a manufacturer, we see the demand for this compound increasing with expanded applications in both traditional medicinal chemistry and new materials science. Process chemists trust our supply because every detail—particle morphology, crystal habit, and even packaging inertness—has undergone real-world trial and error. This isn’t a commodity; each improvement we make translates into time saved and resources preserved for our partners.
The evolving landscape of pharmaceutical and specialty chemical production demands agility from every supplier in the chain. 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine, as manufactured here, answers this demand with proven process reliability. Changing regulatory environments and heightened scrutiny on trace impurities continually push us to enhance both our analytical rigor and production precision. Being close to the shop floor lets us catch trends early—whether that means tweaks to drying protocols to satisfy a new API requirement or changes in solvent systems to reduce environmental impact.
Looking ahead, collaboration with research partners and staying active in consortia for sustainable chemistry keeps our product at the leading edge. Demand for cleaner, greener routes pushes us to explore continuous flow synthesis, alternative chlorinating agents, and in-line purity monitoring beyond current industry standards. None of this happens in isolation; careful listening to end-users—from bench chemists to scale-up managers—grounds each innovation in reality, not marketing promise.
Supplying 4,6-dichloro-1H-pyrrolo[3,2-c]pyridine isn’t one transaction—it’s an ongoing relationship built on transparency and reliable outcomes. Customers come back because their teams know what to expect, both in the bottle and in the support we offer post-sale. We treat every lot as a promise: a commitment to handle deviations, share data, and back up every certificate with traceable evidence from our laboratory. Adjusting packaging sizes to minimize waste, offering technical insights into reaction troubleshooting, and helping partners meet tighter specification targets reflect how we put shared success above mere volume.
Producing this compound, day in and day out, sharpens our sense of what matters—not just checklists and numbers but the daily needs of research and production that drive progress in chemistry. Each kilo, every batch, embodies habits built through experience and respect for those downstream who trust us. We see this not only as a transaction but as a partnership, and we wouldn’t have it any other way.