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HS Code |
371361 |
| Iupac Name | 2-bromo-4-chloropyridine-3-carboxaldehyde |
| Cas Number | 168868-63-7 |
| Molecular Formula | C6H3BrClNO |
| Molecular Weight | 220.45 |
| Appearance | Light yellow to yellow solid |
| Melting Point | 66-70°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CN=C(C(=C1Cl)C=O)Br |
| Inchi | InChI=1S/C6H3BrClNO/c7-6-4(3-10)1-2-9-5(6)8 |
| Synonyms | 2-Bromo-4-chloro-3-formylpyridine |
| Storage Conditions | Store at 2-8°C, tightly closed, in a dry and ventilated area |
| Hazards | Irritant, handle with suitable protective equipment |
As an accredited 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Packed in 200kg HDPE drums, 80 drums per 20′ FCL, totaling 16MT. Ensure secure, ventilated, and compliant chemical shipping. |
| Shipping | 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and handled according to relevant chemical safety regulations. Shipping complies with international and domestic transport guidelines, ensuring safe delivery via courier or freight service, typically with tracking and documentation included. |
| Storage | **Storage Description for 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-:** Store in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Avoid contact with skin and eyes. Store at room temperature or as indicated on the manufacturer’s label, ensuring proper chemical labeling and segregation from food and drink. |
| Shelf Life | 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- typically has a shelf life of 2-3 years when stored in a cool, dry place. |
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Purity 98%: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and minimal side-product formation. Molecular weight 220.45 g/mol: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with molecular weight 220.45 g/mol is utilized in fine chemical manufacturing, where precise molecular mass supports accurate stoichiometric calculations. Melting point 42°C: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with a melting point of 42°C is applied in organic synthesis, where controlled melting behavior allows for efficient compound handling. Stability temperature up to 70°C: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with stability temperature up to 70°C is used in heated batch reactions, where thermal stability prevents decomposition during process cycles. Assay ≥98.5%: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with assay ≥98.5% is leveraged in analytical standard preparation, where high assay provides reliable calibration. Particle size <100 μm: 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro- with particle size less than 100 μm is employed in catalyst development, where fine particle distribution enhances reaction surface area. |
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Standing over the reactor, you learn quickly which molecules demand respect and which cooperate willingly. Over years of crafting intermediates for pharmaceutical and agrochemical partners, some compounds have stood out for their performance and reliability. Among these, the 3-Pyridinecarboxaldehyde, with a bromo at position 2 and a chloro at position 4, continues to carve out its own niche.
This molecule results from deliberate, careful work at each step—harsh halogenations, tight temperature control, rigorous exclusion of moisture and oxygen. We start with foundational pyridine chemistry and bring the skills developed through repeated cycles of process optimization. The product emerges as an off-white or pale yellow solid, kept in amber glass to protect from light, in our facility just outside the quality control lab door. We've paired practical know-how with scientific rigor, so our confidence grows every time a new batch meets or beats internal specifications.
Chemical substitution patterns in heterocycles can look like esoteric points, but process chemists and medicinal chemists recognize a difference right away. The 2-bromo function enables cross-coupling routes that expand a customer’s synthetic flexibility, especially with palladium catalysis. Where a customer wants to explore Suzuki or Buchwald-Hartwig couplings, the bromine position allows efficient transformations and smooth scale-ups. The 4-chloro group stands out for its role in directing electron density and controlling regioselectivity in downstream functionalizations. We’ve noticed our clients using this scaffold for structure-activity relationship studies, building libraries with high chemical diversity that meet new biological requirements.
In real practice, subtle differences in substitution patterns translate into time and money saved. Without the right halogens in the right spots, synthesis gets stuck, or the downstream molecules lose their effectiveness. Feedback from our partners has been clear—alternative isomers or simple benzaldehyde derivatives can’t substitute for the reactivity and selectivity gained from this custom-made aldehyde.
We have run through enough campaigns to see how trace impurities, especially related halogenated byproducts, can cascade into severe purification headaches. Over time, we pushed our detection, testing, and purification stages to weed out low-level halide and oxidized byproducts. Each batch of 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-, comes with a chromatogram you can actually understand and trust. Based on years of tight collaboration between the synthesis, purification, and QA staff, every batch can trace its origin down to a specific warehouse drum and date.
A customer builds an intermediate, scales it from bench to pilot up to the plant, and by the end of that chain, the last thing anyone wants is compositional drift. If a batch varies in reactivity, downstream transformations lose yield or show inconsistent performance. From our manufacturing bay, we hear about it right away through feedback loops, and we adapt purification protocols or tweak the sequence, so that each drum heading out gives the same outcome, batch after batch. For us, alpha purity isn’t an advertising slogan, it’s a safeguard embedded into the workflow.
We select our feedstocks based on thorough screening in the early R&D stage, not just the price on a weekly spreadsheet. Sourcing 3-pyridinecarboxaldehyde as a core, we bring in brominating and chlorinating agents only after resolving compatibility concerns. Heat transfer and agitation control during exothermic halogenation decide batch success. We’ve seen what a slight deviation in dry time or an uncalibrated condenser can mean for impurity formation—frequent GC checks and quick corrections prevent most headaches before they grow.
Downstream workup always throws surprises. Our team has tested dozens of aqueous quench protocols, extracting solvent choices, and pH adjustments, so by now, the right “feel” of the aqueous and organic phases guides a technician’s hand better than any old MSDS directive. Rotovap and column conditions get adjusted every campaign after pilot results roll in. Every blue drum of product coming off the last filter plate matches the high-performance requirements set not on paper, but in practice by those of us in the plant who know how bruising product recalls can be.
In the real world, theoretical talk gives way to questions like, ‘Does this aldehyde give a stable imine?’ or ‘Does it survive the cross-coupler or does it need protection?’ Our partners conduct library synthesis, generate SAR leads, and extend each structure out into metabolic stability or cytotoxicity studies. The 3-Pyridinecarboxaldehyde core, flanked by the bromo and chloro, often forms a backbone for anti-infective, oncological, and agrochemical research programs. Each substitution opens doors to new molecular modifications through either C–C or C–N bond construction.
We have received reports of its use as a starting block in kinase inhibitor scaffolds, and in pesticide syntheses where a halogen acts as both an activation handle and an electron-withdrawing group. Beyond drug and crop protection work, process chemists searching for alternatives to more volatile or less stable benzaldehydes give feedback about its temperature resilience and manageable odor profile.
Buyers occasionally ask why they can’t substitute with 2,4-dichloro or plain 3-pyridinecarboxaldehyde. Halogen type and position control reaction rates and selectivity, particularly in Suzuki and Ullmann-type couplings. Our own test comparisons confirm that the bromo at the ortho position activates the ring toward Pd-catalyzed transformations, much better than a chloro. The 4-chloro can withstand lithiation or other strong base conditions, expanding what a chemist can attempt in one-pot reactions.
Alternative products such as 2-bromo-6-chloro isomers show different reactivity patterns and often require lengthier or less efficient routes, defeating the cost savings. Products lacking either halogen can show more side reactions or yield unacceptably high byproducts after scale-up. We’ve worked through purification and storage comparisons directly—the 2-bromo-4-chloro compound withstood light and ambient temperature better than the 2,6-isomer, reducing concerns about degradation before use.
Another practical benefit: bulk handling. Substitution pattern affects hygroscopicity and storage requirements. The 2-bromo-4-chloro aldehyde sits in a middle ground: not overly sensitive, not prone to runaway oxidation on the shelf, making both warehousing and inventory management simpler for everyone in the chain, from shipping clerk to end-user.
Color and melting range are more than academic footnotes. Out-of-spec color usually signals hydrolyzed or over-oxidized byproduct. Our technicians conduct fresh melting point checks for each campaign, recording not only what the instrument reports, but noting physical feel—any stickiness, clumping, or unexpected volatilization. From the earliest R&D notebooks, patterns have revealed themselves: slight yellowing hints at extended exposure to light or high humidity during the drying cycle.
Thin Layer Chromatography (TLC) and HPLC traces give a snapshot, but GCMS allows our QC team to spot even subtle differences batch-to-batch. This level of attention means end-users never get surprised by a hard-to-remove impurity or need to jury-rig new isolation conditions. If anything strays, we adjust—either reprocess, re-filter, or dig deeper into our supply chain for a root cause. Analytical transparency meets hands-on practicality in every kilo.
We never underestimate the daily realities of storage and handling. The 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-, packed in amber glass or HDPE drums, resists spontaneous decomposition and avoids frustrating lump formation. Drivers and warehouse staff prefer it, because there’s no caustic odor or fume-heavy issues found with similar nitro-aldehyde compounds.
We’ve tested each packaging run for seal integrity and sample retention, particularly when destined for humid or hot locations. Warehouses without premium climate control get nervous about sensitive organics: our compound comes with low risk for sudden self-reaction, and accidental exposure does not cause runaway hazards. The warehouse manager tracks stability data batch-by-batch, noting that product from last season performs just like a fresh batch. This gives peace of mind across the supply chain—from shipping to the end lab bench.
The most experienced plant operators know regulatory changes travel faster and further now than ever before. Data sheets and environmental impact audits form a part of every production campaign. We actively reduce halide waste by reclaiming solvents and optimizing filtrate washes. Our in-house treatment neutralizes most waste before it leaves our yard—no small feat, given local discharge regulations.
Recent years brought stricter attention to hazardous air pollutants. We responded with improved scrubber units and extra vent control in our halogenation bays. This keeps our emissions under occupational health thresholds and minimizes environmental impact. Our compliance documentation gets checked by outside auditors every quarter, so we maintain clarity and real-life credibility with each file, shipment, and regulatory update.
Customer partners in Europe and Southeast Asia remind us that REACH and other frameworks demand not only technical data but detailed traceability. Our documentation team works in tandem with the production floor so every lot moving through our yard meets transparency and reproducibility requirements. This minimizes customs issues and prevents costly hold-ups at ports.
Continuous manufacturing improvement doesn’t take the form of grand pronouncements. Our synthesis teams test new purification techniques, solvent swaps, or automation upgrades in small, practical increments. If a new reagent source introduces unpredictable behavior, we catch it early through extra small-scale runs. Our shift leaders encourage technicians to log every deviation, so even a minor foaming episode or slower filtration rate helps inform the next optimization tweak.
Laboratory data collide with physical realities. For example, attempts to use certain green solvents introduced unanticipated hold times or separation issues. We now rotate improved recycling and solvent cleanup trains into pilot campaigns, prioritizing methods that reduce operator exposure and cut waste. By refining each operational detail—heating rates, ether recovery, phase separations—the end product achieves consistency not only in structure but also in workability day to day.
Over the years, the number of times a partner’s project succeeded or failed based on intermediate quality left a deep impression on us. The real value of 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-, lies in real-world outcomes: smooth pilot scale-ups, high-yield transformations, and reliable project delivery. Direct communications with downstream scientists and manufacturers allow us to respond nimbly—whether that means adjusting batch sizes or improving lot documentation based on partner feedback.
The trust we've built up doesn’t rest solely on a spec sheet or a signature. It grows out of repeated, transparent dialogue—a shared effort to bring chemical ideas to tangible, useful products that withstand the practical stresses of daily use. Each project’s conclusion traces its roots back to the first kilo of pure, on-spec intermediate. This confidence, hard-won through trial and error, forms the real substance underneath every flask, drum, or sample we ship.
The 3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-, stands as more than a niche catalog entry. Its importance comes from its real impact on synthesis for pharmaceuticals and agrochemicals. It advances novel drug programs, supports efficient scaling, and simplifies supply logistics for everyone from the R&D bench scientist to the plant chemist. Its specific structure creates uniquely effective synthetic opportunities that no generic substitute can easily match.
Every step that led to its repeatable, high-purity form—tested, tweaked, and proven in an actual manufacturing environment—makes it a dependable tool for innovators working at the intersections of chemistry, biology, and technology. Our experience shows that behind every successful application lies a team of hands-on manufacturers who ensure reliability not by accident, but by intention and careful control.