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HS Code |
428819 |
| Chemical Name | 4-Chloro-2,3-dimethylpyridine-N-oxide |
| Molecular Formula | C7H8ClNO |
| Molar Mass | 157.6 g/mol |
| Cas Number | 136504-63-9 |
| Appearance | White to off-white solid |
| Density | Approx. 1.2 g/cm³ (estimated) |
| Solubility | Soluble in organic solvents, slightly soluble in water |
| Smiles | CC1=NC(=C(C=C1Cl)C)[N+](=O)[O-] |
| Inchi | InChI=1S/C7H8ClNO/c1-5-7(10(9)11)6(2)3-4-8-5/h3-4H,1-2H3 |
As an accredited 4-Chloro-2,3-dimethylpyridine-N-oxide 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, tightly sealed, labeled with '4-Chloro-2,3-dimethylpyridine-N-oxide' and appropriate hazard symbols. |
| Container Loading (20′ FCL) | 20’ FCL can load approximately 14-16 MT of 4-Chloro-2,3-dimethylpyridine-N-oxide packed in 25 kg fiber drums. |
| Shipping | **Shipping Description:** 4-Chloro-2,3-dimethylpyridine-N-oxide should be shipped in tightly sealed containers, protected from light and moisture. Store at ambient temperature, away from oxidizers and acids. Comply with local, national, and international regulations. Properly label as a chemical substance. Ensure packaging prevents leakage and damage during transit. Handle with appropriate safety precautions. |
| Storage | Store 4-Chloro-2,3-dimethylpyridine-N-oxide in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Protect from light, moisture, and sources of ignition. Ensure proper labeling and restrict access to trained personnel. Follow standard laboratory safety protocols and ensure availability of safety data sheets (SDS). |
| Shelf Life | Shelf life of 4-Chloro-2,3-dimethylpyridine-N-oxide: Typically stable for 2–3 years when stored in a cool, dry place. |
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Purity 98%: 4-Chloro-2,3-dimethylpyridine-N-oxide with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced contaminant formation. Melting Point 84°C: 4-Chloro-2,3-dimethylpyridine-N-oxide with a melting point of 84°C is used in solid-state formulation processes, where it provides thermal stability during manufacturing. Molecular Weight 157.60 g/mol: 4-Chloro-2,3-dimethylpyridine-N-oxide with a molecular weight of 157.60 g/mol is used in medicinal chemistry research, where it offers precise stoichiometric control in compound development. Particle Size <50 µm: 4-Chloro-2,3-dimethylpyridine-N-oxide with particle size less than 50 µm is used in fine chemical synthesis, where it enables efficient dissolution and homogeneous reactions. Stability Temperature 120°C: 4-Chloro-2,3-dimethylpyridine-N-oxide stable up to 120°C is used in high-temperature organic transformations, where it maintains structural integrity and minimizes thermal degradation. Solubility in DMSO 10 mg/mL: 4-Chloro-2,3-dimethylpyridine-N-oxide with DMSO solubility of 10 mg/mL is used in bioassay development, where it delivers consistent concentration profiles for accurate activity assessment. |
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As a chemical manufacturer with decades of production floor experience, I can see how 4-Chloro-2,3-dimethylpyridine-N-oxide holds its own in niche pyridine chemistry. This compound stands out once the strengths behind its molecular structure are understood. With two methyl groups at the 2 and 3 positions, and a chloro at the 4, the N-oxide function introduces a unique electronic profile that takes the raw reactivity of pyridine rings in a new direction compared to its direct relatives. In nearly every batch we produce, I see how these subtle changes impact solubility, electrophilic strength, and compatibility, which shape how formulators use it in advanced synthesis.
There’s nothing hypothetical about the process: we run the reactors, filter every lot, and check purity levels with regular HPLC and NMR backup tests. Our typical product achieves high purity—over 98% by assay—confirmed by the plate and column. This is no small feat, given that side products in N-oxide chemistry resist easy exclusion. We pay close attention to moisture control, crystalline morphology, and trace chloride byproducts, since these contaminants would limit performance, especially for researchers pushing for highly selective oxidations or seeking a stable building block in agrochemical intermediates.
We favor a solid crystalline form, pale with a light, needle-like appearance for ease of handling. Throughout storage, maintaining consistently low water content below 0.5% has prevented caking and shifting in melting profiles. This looks trivial on paper, but those who’ve tried less-careful batches from other sources know what difference it makes in the flask. Every round of inspection, from the visual examination under the lamp to FTIR, proves out this attention to detail.
Users do not come to this compound for a generic N-oxide effect. They reach out for its edge in oxidation reactions—specifically, mild but highly selective oxidation where over-oxidation must be avoided. Its electron distribution opens up pathways for asymmetric catalyst design, while the methyl and chloro groups shift the ring’s reactivity profile. In our experience, the biggest demand comes from teams exploring intermediate stages of pharmaceuticals, where the N-oxide's electronic tuning allows for partial oxidations or controlled reductions later in the synthesis. More than once, a customer targeting novel fungicides or insecticides has looked to our product's reliable performance for safety and efficiency, reasoning from our QC data that there won’t be batch-to-batch surprises.
Beyond fine chemicals, we’ve seen R&D groups trying to convert similarly structured heterocycles and needing a starting point with specific reactivity trends. The N-oxide motif supports ligand design in transition metal catalysis, often facilitating unique selectivity patterns not reached with plain pyridines or even other pyridine N-oxides. Time after time, the strength of this compound lies in its predictable handling and robust behavior under reaction conditions. Whether the scale is sub-gram or hundred-kilogram, the response is similar: reliable activation, easier work-up, and less post-processing for byproduct removal. This saves valuable cycles in both pilot and full-scale facilities, a point sometimes overlooked by those outside the plant floor.
Some new buyers ask why they should not just stick to generic pyridine N-oxides, or purchase mixtures from resellers. The answer is obvious once you grind through a few reactions yourself: most standard pyridine N-oxides lack the precise electron-withdrawing and donating influences shaped by the chloro and methyl substitutions at play here. That means yields can sag, and impurity profiles shift away from acceptable thresholds. Synthetic chemists quickly catch on to the cleaner baseline delivered by a genuine, well-made 4-Chloro-2,3-dimethylpyridine-N-oxide.
Compared to 2,3-dimethylpyridine-N-oxide, adding the 4-chloro group transforms the reactivity and changes compatibility with halogen-sensitive partners, which opens new doors for cross-coupling or reductive removal steps. In contrast, substituent-free versions tend to spread their activity too broadly, yielding unwanted byproducts when specificity is needed most. Over the years, I’ve seen that the backbone’s clean separation from other ring-substituted analogs translates into fewer side reactions, especially when pushing large-scale multi-step syntheses with expensive catalysts. Downstream cleanup eases, lowering the risk of contamination—especially critical in pharmaceutical or food-relevant supply chains that will not tolerate off-flavors or unknowns.
Many compare it to trade-named variants, solvent-wet blends, or impure or crude forms found on the open market. Time after time, the result is an upsurge in yield loss, filtration issues, or inconsistent stoichiometry. Experienced plant operators recognize that purchasing direct from a manufacturer—with nothing diluted, stretched, or cut with stabilizers—brings certainty to process development. You do not run the risk of hidden stabilizers, mixed crystal phases, or recycled solvent residues that can ruin a batch’s performance, especially at scale.
Manufacturing 4-Chloro-2,3-dimethylpyridine-N-oxide demands deep respect for reaction kinetics and purification. Years back, inadequate chloride scavenging led to corrosive side reactions and yield drops; it took hands-on experimentation to optimize reactor design and temperature holds. This type of experiential knowledge does not show up on safety sheets or specs but manifests in better process reliability, tighter control over particle size, and smoother filtration. It’s worth the investment in process upgrades to fully guarantee sharp crystallinity and minimize amorphous impurities.
Each campaign reminds us how handling N-oxides requires tight environmental controls. Over-drying can induce static issues, increasing the risk of clumping or airborne spread. Under-drying shortens shelf life and reduces reliability, as moisture-sensitive customers have pointed out in case discussions. The value of a trusted manufacturer appears in these moments: not just supplying but optimizing each kilogram, ensuring the resulting intermediate or end product meets the expectations of the end users, not just the paperwork criteria.
We draw on a record of repeated quality checks, with every lot confirmed by spectral analysis. FTIR scans line up with published assignments; NMR shows the expected methyl and chloro signatures, exactly where the literature places them. Purity routinely exceeds 98%. On orders where the end use called for even tighter specs, our team has managed to push purity above 99% using column intervention, albeit at a cost premium. Every complaint or deviation report feeds back into process tweaks. Last year, a single batch flagged for excessive particle size prompted a complete overhaul of the drying zone to prevent similar issues in the future.
The supplemental documentation provided to our regular clients reflects not generic cut-and-paste, but precise, batch-specific data. There are real advantages in supplying direct from the source: chain-of-custody is verifiable from raw material through to finished drum, with no unexplained stops in between. This level of control satisfies auditors and provides researchers the confidence that their experimental reproducibility is not threatened by hidden changes in reagent source or stability.
Some buyers have historically relied on imported bulk intermediates blended or partially purified by traders. These routes often turn up issues: substances arriving with inconsistent water content, oddball off-notes, and conflict between documentation and analytical reality. The manufacturing side has an answer: rigorous lot tracking, on-site spectral verification, and, if needed, custom drying or grinding services to hit the customer’s ideal form factor.
Handling feedback does not end with the sale. Companies regularly update us about their test results, which loops into batch improvement. An international client switching from open-market sources to our controlled product line saw a 10% rise in usable yield and eliminated off-color byproducts in their pharmaceutical intermediates. The reactionary pattern in less-controlled procurement methods—cleaning out reactors more often, planning additional purification cycles, or dealing with odd odors—vanished. This clear feedback loop shapes not just our product, but the broader reliability of the customer’s operations. Speaking from hands-on knowledge, when the logistics team hands off drums bearing our own seal rather than that of an anonymous repacker, you know exactly what to expect every time.
Conversation with formulation chemists brings up a recurring theme: ease of integration, steady reactivity, and absence of unpredictable residues. They appreciate being able to match spectroscopic fingerprints batch after batch and avoid the headaches introduced by trader-blended material. Over dozens of successful lots, we have measured the repeatability of elemental analysis, the absence of unwanted peaks, and strong correlation with industry benchmark values.
Experienced chemists quickly spot the lack of haze, the sharp melting point, and the absence of extraneous features when working up reactions. I cannot count the number of times our technical calls have resolved disputes about the cause of erratic behavior in similar N-oxide products. Ultimately, a batch that needs no remedial cleanup, extra washing, or laborious filtration is more valuable than a marginally cheaper alternative. This translates into saved labor and lower waste disposal costs—outcomes tracked on any well-managed project’s bottom line.
Lab-scale synthesis brings out product nuances that grow exponentially at the plant level. 4-Chloro-2,3-dimethylpyridine-N-oxide’s stability and tight melting range allow safer heating cycles, meaning fewer decompositions or discolorations during upscaling. We’ve received reports from plant engineers that switching away from questionable variants resulted in fewer stuck filters and less downtime, which means more throughput and less overtime spent on post-batch cleaning.
Process chemists share stories about the bumps and hurdles faced with impure alternatives: colored solutions, slow dissolving rates, or unpredictable reactivity under catalysis. Subtle impurities from under-controlled manufacturing may seem harmless but can become catalytically active, causing side reactions. True lot-controlled product delivers uniform, timely response—crucial in continuous runs or campaigns where any exception can ripple through schedules and budgets.
Compliance isn’t a theoretical goal; for us, it comes from daily routines—meticulously minimizing waste, managing solvents, and recording every lot. Experience taught us that using quality-controlled 4-Chloro-2,3-dimethylpyridine-N-oxide lessens regulatory headaches for both the manufacturer and user. Purity and documented chain-of-custody cut down on batch re-testing, regulatory queries, and bureaucratic overhead, especially during audits for pharmaceutical, agrochemical, or specialty chemical applications.
Well-made product means less need for rework or disposal. By reducing unnecessary side reactions, the downstream burden on effluent systems is kept to a minimum. This reduces not only costs but also environmental emissions. Knowledge forged through years at the bench shows that tight control in the pyridine N-oxide line delivers indirect benefits in stakeholder confidence and reduces the stress of unexpected compliance interventions.
Direct producer feedback, rather than indirect reports, has repeatedly improved both our product line and client satisfaction. Each customer discussion feeds directly into plant changes—whether it’s adjusting drying times to get statically free flow or altering sieve mesh for consistent particle size. Our facility’s trend data from returned feedback logs supports a steady reduction in off-spec product, shrinkage, and reprocessing events year-on-year.
Market reports covering trader-led deliveries often mention inconsistent responses under scale-up or in downstream application. This pattern does not occur from trusted, direct-sourced batches. Lessons derived from decades of manufacturing efforts—watching for subtle discoloration, monitoring for evolving odor, checking for trace side products—result in a practical guarantee that simply cannot be replicated by traders without plant-level oversight.
Buyers seeking to leverage the full performance potential of 4-Chloro-2,3-dimethylpyridine-N-oxide benefit from choosing manufacturers with open access to batch records and an attitude of direct technical support. Those willing to work with producers capable of real-time adjustment—whether in grind, drying level, or packing—see not just a smoother ordering process, but ultimately a reduction in downstream cost and process inconsistencies. Investing by partnering directly with those who oversee synthesis, drying, QC, and shipping day in and day out, avoids needless complications in later stages of formulation and application.
For users experimenting on new reaction pathways, engagement with knowledgeable suppliers accelerates method development, since feedback loops from the floor—rather than distributors—can offer process advice grounded in hard-won experience. Many breakthroughs reported with this compound sprang from direct manufacturer support: real-time process tweaks, access to up-to-date lot tracking, and a willingness to take direct phone calls about technical phenomena. This interaction not only supports better outcomes for first-generation projects, but opens channels for process optimization based on ground-level facts.
Across years of plant work, I’ve found that the most reliable tool in the toolbox is a compound made with diligent, hands-on control. 4-Chloro-2,3-dimethylpyridine-N-oxide fills a demanding role in laboratory, pilot, and commercial settings by providing reproducible, traceable, and well-characterized N-oxide functionality. The difference from the source end shows up all the way to finished product: fewer headaches, streamlined processing, and less wasted time. Purity above 98% is expected, not offered as a premium, and every batch yields data that closes the feedback loop with our partners in R&D and production. Those who invest in quality-controlled supply discover that in real-world terms, fewer process interruptions and more predictable chemistry mean true value beyond the laboratory scale.