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HS Code |
746265 |
| Product Name | 2-Bromo-5-chloropyridine-4-carboxaldehyde |
| Cas Number | 876123-62-9 |
| Molecular Formula | C6H3BrClNO |
| Molecular Weight | 220.45 |
| Appearance | Light yellow to brown solid |
| Melting Point | 74-77°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in common organic solvents |
| Smiles | C1=CN=C(C=C1Br)C(=O)Cl |
| Inchi | InChI=1S/C6H3BrClNO/c7-5-1-4(3-10)2-9-6(5)8 |
| Synonyms | 2-Bromo-5-chloro-4-formylpyridine |
| Storage Temperature | Store at 2-8°C |
| Hazard Class | Irritant |
As an accredited 2-Bromo-5-chloropyridine-4-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a red screw cap. Labeled with chemical name, hazard symbols, and batch number. |
| Container Loading (20′ FCL) | 20′ FCL container loading ensures secure, moisture-proof packing of 2-Bromo-5-chloropyridine-4-carboxaldehyde in sealed drums or cartons. |
| Shipping | 2-Bromo-5-chloropyridine-4-carboxaldehyde is shipped in sealed, chemical-resistant containers, compliant with international chemical transport regulations. It is labeled as hazardous and handled as per MSDS guidelines, ensuring temperature control and protection from moisture and light. Shipping documentation includes relevant safety, hazard, and handling instructions for regulatory compliance and recipient safety. |
| Storage | **2-Bromo-5-chloropyridine-4-carboxaldehyde** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers, acids, and bases. Store at room temperature or as specified on the manufacturer’s label. Ensure proper labeling and follow all relevant safety and handling guidelines. |
| Shelf Life | Shelf life of **2-Bromo-5-chloropyridine-4-carboxaldehyde** is typically 2–3 years when stored in a cool, dry, and sealed container. |
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Purity 98%: 2-Bromo-5-chloropyridine-4-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent reaction yields. Melting Point 94-97°C: 2-Bromo-5-chloropyridine-4-carboxaldehyde with a melting point of 94-97°C is used in solid-state reactions, where precise melting characteristics enable controlled crystallization. Molecular Weight 236.46 g/mol: 2-Bromo-5-chloropyridine-4-carboxaldehyde with molecular weight 236.46 g/mol is used in medicinal chemistry research, where accurate molecular weight facilitates dosage calculations. Particle Size <50 µm: 2-Bromo-5-chloropyridine-4-carboxaldehyde with particle size less than 50 µm is used in fine chemical formulation, where uniform particle distribution enhances dispersion in solvents. Stability Temperature up to 60°C: 2-Bromo-5-chloropyridine-4-carboxaldehyde with stability temperature up to 60°C is used in storage and transport processes, where thermal stability minimizes degradation. Water Content ≤0.5%: 2-Bromo-5-chloropyridine-4-carboxaldehyde with water content ≤0.5% is used in anhydrous synthesis routes, where low moisture content prevents unwanted hydrolysis. |
Competitive 2-Bromo-5-chloropyridine-4-carboxaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
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Every kilogram of 2-Bromo-5-chloropyridine-4-carboxaldehyde that ships out of our facility bears the story of thousands of hours spent in development, adjustment, and scale-up. No third party stands between us and the chemists who specify the tight tolerances that underpin reliable synthesis. We have seen demand for this intermediate grow not because it sounds cutting-edge, but because it delivers the specific results process chemists and researchers want for downstream syntheses, particularly in pharmaceutical, agricultural, and fine chemical fields. The supply sometimes lags behind market interest—this isn’t a product that comes off a commodity line—but over years, we’ve learned how to turn uncertain pilot batches into robust, scalable production that meets the accuracy modern synthesis expects.
Several years back, one of our large pharma clients needed access to this carboxaldehyde at short notice. Their earlier source—an outside trader reliant on unknown origin material—ran into supply chain bottlenecks. We stepped in, documenting every aspect: the selection of pyridine precursors, bromination and chlorination sequence, the control of formylation conditions. Only by holding ourselves accountable from reaction pot to packaging did we build trust that lasts longer than the next shipment. Such transparency rarely comes from mere middlemen. Without direct control, the risk of byproducts mounts, yields sag, and downstream yields on multi-step processes drop—which no chemist can afford once the project scales out of the lab. We see time and again: it’s the critical starting point molecules like 2-Bromo-5-chloropyridine-4-carboxaldehyde that make or break entire project timelines.
Unlike near neighbors in the substituted pyridine family, this compound offers developers a particularly responsive carboxaldehyde handle at the 4-position. The ring pattern—bromine at the 2-position, chlorine at the 5-position—signals reactivity that supports selective couplings, cross-couplings, or nucleophilic substitution. We work daily with synthetic groups that need to functionalize specific points on the pyridine ring. Even a subtle shift in substitution pattern—say, moving the chloro group to another carbon—means entirely different reactivity and undesired side products. A clean sample of 2-Bromo-5-chloropyridine-4-carboxaldehyde, confirmed by NMR, GC, and HPLC, saves days of troubleshooting that few project leads can spare.
Getting the “Aldehyde” axis right is critical. Over-oxidation, incomplete conversion, or the presence of residual starting material can make the downstream reactions unpredictable. We learned, early in the scale-up phase, that minor system leaks or trace water in a key stage would allow hydrate formation or adventitious side reactions—not that evident in small flasks, but disastrous in 250-liter glass-lined reactors. Each batch record we fill in represents knowledge hard-won on the shop floor, not imagined in an office high above the factory.
It’s one thing to read a published protocol, another to watch what happens inside a commercial reactor. Temperature control, mixing speeds, and order of reagent addition all come under the microscope during our process trials. Literature methods often ignore how trace metal impurities in raw starting pyridine will skew bromination selectivity. Early on, we saw that haphazard sourcing of such basics introduced extended purification headaches downstream—so we took steps to qualify only suppliers willing to back up their quality by regular re-analyses.
This vigilance pays off in the reduction of colored, impure, or variable batches. For customers used to dealing with traders, that kind of batch-to-batch consistency is an eye-opener. Our own team expects to see each analytical report before proudly affixing batch labels. We have found specification drifts—such as inconsistent melting points or unexplained mass spectrometric signals—whenever the manufacturing pipeline grows too remote from final quality oversight. Somebody on the shop floor, with experience pouring real solutions and troubleshooting cryogenic additions, always reviews the run sheets and data. Automation helps, but never replaces the intuition that comes only from hands-on chemical manufacturing.
Dishonest shortcutting or casual re-packaging slips into chemical supply more than many realize. Several times a year, we get requests for “substitutes” or “analogs” from buyers burned by inconsistent supplies of this compound. Substitution isn’t simple—no competent chemist swaps in a 2-chloro analog merely because a trader offers it cheaper. One major customer, developing advanced intermediates for a new agrochemical, once struggled for weeks to reproduce a cyclization after using material from a third party. We analyzed a retained sample—the NMR and IR spectra betrayed the presence of residual solvent and unidentified aromatic byproducts. Even parts per thousand can poison entire reaction schemes, especially in scale-up. We don’t cut steps; purity from us means numbers you can build a synthesis on.
Pricing in bulk markets is volatile. Some distributors claim to source from manufacturers; rarely do they disclose how many hands pass between the originator and the end-user’s bench. Since we own the process, we never have to guess origin. Our archives retain batch traceability back to raw materials. If an issue arises, direct communication between our technical team and yours circumvents weeks of guesswork. Faster resolution, less project downtime, and more predictable outcomes—all these matter deeply to users who stake their programs on timely delivery and reproducible lots of this pyridine carboxaldehyde.
We don't just count on typical assay values or a single HPLC reading. Over years we evolved a verification process involving NMR, GC-MS, moisture analysis, and (where required) elemental analysis. The 2-Bromo-5-chloropyridine-4-carboxaldehyde leaves our facility only when that lot passes the strictest standards set by both internal protocols and major global clients. Lowering detection limits for trace sympathizers and unknowns takes extra hours on each batch, but feedback from repeat customers convinces us it’s the right investment.
Handling a sensitive aldehyde function means protecting against racemization, oxidation, or unintended condensation. Product stored under nitrogen, in low-light conditions, inside HPLC-grade containers, holds up months longer than inadequately protected bulk material. Chemists notice the difference as improved shelf life and cleaner performance in condensation or reductive amination reactions. In fields where each downstream transformation relies on ultrapure building blocks, “close enough” does not satisfy. Every additional purity check we add emerged from our own root-cause analyses whenever a downstream user flagged an issue—even if it was one in five thousand batches. Manufacturers on the ground have the incentive (and ability) to fix problems at the root, rather than papering them over or blaming another link in the chain.
In active pharmaceutical ingredient synthesis, this molecule forms a backbone for new heterocyclic assemblies, often serving as a launchpad for further ring construction or cross-coupling reactions. The precision by which the carboxaldehyde group participates in Wittig or reductive transformations sets the compound apart—it acts as a strategic launching point for adding complexity. Our customers, who typically run either iterative library syntheses or scale up to pilot kilo batches, trust that intermediates made from our 2-Bromo-5-chloropyridine-4-carboxaldehyde won’t introduce surprises downstream.
Agrochemical researchers building new actives for crop protection often request batches tailored to ongoing SAR (structure–activity relationship) studies. No two development pipelines look alike: some need large single lots for a multi-year scale, others prefer small, frequently delivered quantities so that they never commit too much capital at an early stage. Only a manufacturer able to flex their process quickly, backed by process data banked from hundreds of prior runs, can respond to such diversity. Flameless reactors, rapid cooling, and full hazard analysis are part of our culture, not optional extras.
Here’s where our hands-on knowledge changes the facts on the ground. Chemists sometimes attempt to work around a shortage of 2-Bromo-5-chloropyridine-4-carboxaldehyde by switching to other bromopyridines, only to discover the hard way that electron density and ring substitution patterns alter both yield and selectivity. While 2-Bromopyridine, 5-Chloropyridine, or 2,5-dibromopyridine exist as stock options, none bring the same reactivity as the precise 2-bromo/5-chloro/4-aldehyde substitution. Direct feedback from users tells us that even switching the position of the formyl group or the halogen leads to isolation headaches, more complicated purification, and off-target isomers. Our in-house analytical chemists see this in impurity profiles—unique fingerprints emerge for each isomeric or regioisomeric variant.
A vivid case involved a synthetic chemist attempting to circumvent a backlog with an “almost equivalent” isomer. A high-value amide coupling failed; the side products tracked with the NMR showed that activation was either too sluggish or the selectivity had skewed entirely. No amount of extra coupling agent or temperature adjustment rescued the yield. It took reverting to our precise 2-Bromo-5-chloropyridine-4-carboxaldehyde, meticulously purified, to restore the clean conversion—the value was self-evident. Hard lessons like this underline why tiny deviations in building block structure can sabotage whole projects, especially when downstream regulatory filings depend on batch-to-batch consistency.
The chemical supply world is never static. New downstream applications appear with little warning—customers in material science recently started using this building block in electronic device research, testing new conjugated systems. The core requirements don’t change: in all these uses, it all comes back to having a source that understands how to adjust process variables under real-world constraints. As pressure mounts for sustainable chemistry, we look at solvent selection, energy optimization, and recycling wherever practical. Our engineers not only optimize yields and selectivity, but also minimize waste and energy usage because at scale, those decisions add up—environmentally and economically.
Supply shortages, logistics disruption, and regulatory changes present constant hurdles. Having everything in-house—development, scale-up, QA—equips us to adjust shipments, alter packaging, or provide custom documentation as regulations shift. Others relying on multiple outside partners get mired in red tape whenever a customer’s needs go beyond “off-the-shelf” expectations. We believe innovation belongs on the shop floor as much as in the lab. Open communication with the R&D community guides our next process improvements; we routinely invite input on packing formats, allowable trace metals, sustainability priorities, and lot sizes. Responsive manufacturing shortcuts endless back-and-forth and lets researchers concentrate on invention, not procurement headaches.
The move to low-volume, high-value intermediates places new demands on global chemical supply. Directly manufactured 2-Bromo-5-chloropyridine-4-carboxaldehyde stands apart because it brings a legacy of iterative improvement: tweaks to reactor loads, cleaning protocols, improved analytical tools, and a habit of learning from every deviation. Our approach means that the focus never flickers from the essentials—purity, traceability, and technical support straight from the people who actually made the material.
All the talk in the world about “quality assurance” means far less on paper than the confidence laboratory teams find when a batch gives the results they expect, run after run. Our compound isn’t just produced for the shelf; it’s manufactured for the scientists who unlock new reactions, scale them up, and push their fields forward. Each drum, each bottle, bears not only a label but the experience of the chemists, analysts, and operators who care about every step on the journey from raw material to your bench. That is the promise of truly direct manufacture.