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HS Code |
528111 |
| Productname | 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride |
| Casnumber | 86604-75-3 |
| Molecularformula | C8H11Cl2NO |
| Molecularweight | 208.09 g/mol |
| Appearance | White to off-white powder |
| Purity | Typically ≥98% |
| Meltingpoint | 170-174°C |
| Solubility | Soluble in water, methanol, and ethanol |
| Storagetemperature | 2-8°C (Refrigerated) |
| Synonyms | 2-(Chloromethyl)-4-methoxy-3-methylpyridine hydrochloride |
| Iupacname | 2-(Chloromethyl)-4-methoxy-3-methylpyridine hydrochloride |
| Hazardclass | Irritant |
| Smiles | COC1=CC(=C(C=N1)CCl)C.Cl |
| Uses | Pharmaceutical intermediate |
As an accredited 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle sealed with a screw cap, labeled with hazard symbols and product details for 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride securely packed, labeled, and palletized, ensuring safe transportation and compliance with regulations. |
| Shipping | 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride should be shipped in tightly sealed, chemical-resistant containers. It must be clearly labeled and handled according to local regulatory requirements. The package should be protected from moisture and stored at room temperature. Ensure transportation in compliance with all hazardous material guidelines to prevent exposure or accidental spillage. |
| Storage | 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature, and handle under an inert atmosphere if possible. Ensure proper labeling and access only to authorized personnel. |
| Shelf Life | 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride typically has a shelf life of 2 years when stored in cool, dry conditions. |
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Purity 98%: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield coupling reactions. Melting Point 145°C: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride with a melting point of 145°C is used in solid-phase organic synthesis, where it provides thermal stability during processing. Particle Size <50 µm: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride with a particle size less than 50 µm is used in fine chemical formulation, where it enables uniform dispersion and reactivity. Water Content <0.5%: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride with water content below 0.5% is used in moisture-sensitive chemical processes, where it minimizes hydrolysis and degradation. Molecular Weight 208.08 g/mol: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride with a molecular weight of 208.08 g/mol is used in structure-based drug design, where exact stoichiometry ensures reproducible outcomes. Stability Temperature <80°C: 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride stable below 80°C is used in temperature-controlled synthesis, where it prevents decomposition and maintains product integrity. |
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Every production run brings fresh insights. Our mainline 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride delivers high purity to organic synthesis specialists who demand both consistency and scalability. In years of routine operation, we have refined process parameters through hands-on batch monitoring, not just theoretical optimization. The choice to manufacture this compound hinges on its unique profile that supports demanding alkylation reactions, particularly for pharmaceutical intermediates where substitution patterns on pyridine rings dictate biological results.
Raw material sourcing shapes the final outcome. As a manufacturer, we know that any fluctuation in chloromethylating reagent supply impacts impurity profiles. Keeping upstream lines selected for trace metal content controls failures in downstream transformations. Other products in the chloromethylated pyridine category often carry higher levels of residual solvents, notably dichloromethane, which complicates isolation when scaling up kilo and multi-ton runs. Our vacuum distillation steps—not commonly used by traders—allow a more robust crystallization and consistent particle size, which brings smoother handling right through to formulation.
Our principal product corresponds to the hydrochloride salt, which brings advantages over the base. When we started with the free base in experimental batches, you found a greater hazard profile: more volatility, more stringent containment requirements, and frequent bumps in solvent use for phase separation. By producing the hydrochloride, we maintain stability and suppress volatility. This matches what downstream pharmaceutical labs expect, both for storage safety and reproducible behavior under their reaction conditions. Our standard batch size can flex from kilo-scale custom orders up to regular multi-ton lots for long-term partners, all without trading off critical purity specifications.
Chemists turn to this compound in heterocyclic building for several anti-infective and CNS candidate molecules. Unlike generic methylpyridines, our product's methoxy and methyl substitution pattern on the 3 and 4 positions directs selectivity in your alkylation stage, which becomes critical in avoiding unwanted regioisomers. The chloromethyl group functions as a precise electrophile—reacting under mild base and temperature. We have watched process teams reduce reaction steps by leveraging this reactivity. You gain efficiency, reduce waste, and see cleaner analytical profiles with less work-up.
Operating day-in and day-out, we’ve encountered the small differences that textbooks rarely cover. Our chemists found storage humidity must be below 45 percent. Drier rooms reduce caking and prevent slow but problematic hydrolysis that degrades both appearance and reactivity. We have strengthened our packaging line by double lining and using antistatic bags, after learning that clumping in larger drums sometimes held up scale-up at client sites. Each time challenges arose, immediate feedback with the synthesis team improved outcomes for the next batch.
Purity is not just a spec line in our daily reports—it’s a guarantee we check ourselves every shift. We worked closely with our QA to move beyond baseline HPLC checks. By adopting advanced LC-MS and trace ion analysis, our team reduced unknown impurities below 0.1 percent, especially those critical to medicinal chemistry partners. We have seen firsthand how small residuals in the hydrochloride—often overlooked elsewhere—can slow downstream bromination or fluorination steps. More than once, feedback from a customer’s pilot line has steered us to tune in-process controls. Any variance seen in the probe goes right back to the floor for careful adjustment in the next batch.
Not all pyridine hydrochloride derivatives behave the same. Our experience is that 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride brings both increased ring stability and selective reactivity, especially compared to simple 2-chloromethylpyridine hydrochloride or the basic 4-methoxy isomer. Each functional group on this molecule directs reactivity and solubility in specific ways. Many of our clients initially tried one-pot routes using off-the-shelf methylpyridines, but only shifted once they ran headlong into regioisomer formation and inconsistent yields in purification. The presence of the methoxy group in the 4-position not only tunes its electronic effects but directly reduces byproduct formation. That comes straight from time at the bench and at scale, not just a catalog table.
Nobody likes running into bottlenecks during process scale-up, least of all seasoned process chemists. Our team has seen that solvent switching and humidity changes during transfer can produce lot-to-lot variation in less tightly-controlled operations. By running kilo lab trials using the full suite of on-site reactors and drying ovens, we revalidated our purification. Customers caught in delays from third-party resellers—who usually lack end-to-end control—have relayed how disruptive uneven supply chains can become. In contrast, our ongoing batch process gives direct visibility into every intermediate step, letting us act the moment deviations appear. Open communication and early sharing of in-process samples avoid the all-too-common scramble in final QA release.
We have developed our product specification after years of feedback on application requirements, not as a marketing afterthought. The appearance, melting point, assay, and residual solvent ranges all exist for a reason. A batch that falls outside our standard—whether in particle flow or trace chloride—does not move forward, because in-house failures always cost less than problems for our customers. These limits come from data, not aspiration: multiple stability studies, real-world handling in large stainless drums, and needle development using our clients’ own equipment. It’s not just a checkbox; it’s a sign of work behind the spec.
In recent collaborative trials, our partners found that high-purity 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride simplifies their own process validation. One team in the CNS research field managed to shave off two purification steps from their intermediate isolation, meeting both regulatory and timeline targets. These aren’t one-off stories—we work next to the end users to refine not only material quality but delivery packs and documentation. Our technical group has invested time with customers to model how water content in the hydrochloride correlates with their downstream crystallization problems. If results in the lab deviate from expectations, we adjust our cutoff specs, not ask the customer to work around our supply.
Pharmaceutical teams use our product to build core scaffolds in new drug candidates. Our own pilot runs with innovative biotech partners have demonstrated how this hydrochloride provides a reliable entry point for both exploratory SAR (structure-activity relationship) work and the next phase of scale-up. Custom agrochemical innovators took advantage of its selective electrophilicity to streamline their synthesis of novel plant actives. In every case, our consistency in supply and documentation helps teams focus on their own targets, not on troubleshooting materials that don’t behave as advertised.
As direct manufacturers, we have learned the hard way that strict controls at every processing step minimize workplace hazards. The inherent properties of this hydrochloride mean less inhalation risk compared to open handling of the chloromethyl base. On the environmental front, internally monitored solvent recycling loops and strict atmospheric emissions controls keep operations under regulatory targets. We have worked with local authorities and industrial parks to stay ahead of compliance expectations, so changes in regulatory climate don’t disrupt projects downstream. Certifications are the result, but the motivation comes from direct process experience: staff safety and long-term site viability matter at every step.
Being on the manufacturing line, we see problems immediately—not as customer complaints weeks later. This hands-on approach allowed us to recognize that increasing centrifuge speed in the initial work-up shaved off moisture content and avoided late-stage caking. Another round of trials demonstrated that fine-tuning the chloromethylation stage prevents over-chlorination, which means a smaller crop of unwanted side products. Whenever new formulation challenges emerge at partner companies, our technical service team can quickly adjust batch conditions or suggest process tweaks because we control the plant floor ourselves, not through intermediaries.
Any manufacturer can aim for volume; our development work instead focuses on value-added support. We track every process parameter that matters to downstream labs. Documentation packs include not only batch release data but analytical chromatograms, mass spectra, and details about drying conditions. For formulation scientists trying to deliver robust validations to regulatory agencies, clear and comprehensive data makes the difference between a smooth approval and a project delay. We believe in sharing this depth of analysis—not just meeting minimum regulatory requirements but supporting innovation through transparency.
Our daily experience tells us the biggest risk comes from uncertain or distant supply. Outsourced intermediaries too often pass on unchecked product, causing headaches in GMP audits or batch consistency. Because we maintain direct control from start to finish, issues are identified and managed before shipments ever leave the gates. We work with shipping partners to implement validated moisture barrier drums, reducing exposure and maintaining peak reactivity even during long transit. This degree of traceability stands in contrast to short-term trades seen with other specialty intermediates, and our commitment to stability testing ensures every batch meets the same rigorous benchmarks.
Feedback from experienced process chemists keeps our improvements grounded in real application. When customers ran up against filtration problems in their campaign, faster response times and sampling tests at our end caught batch-to-batch variability before it threatened their schedule. Our technical group visits partner labs, reviewing bottleneck points on-site and suggesting alternate dilution or quenching protocols, all built from data harvested in our own runs. The goal is not just to sell a necessary chemical but to shorten your path from reaction setup to purified intermediate, saving months of troubleshooting.
With regulatory expectations tightening, ongoing work at our site focuses on process intensification—that means greener solvents, energy reduction in drying, and in-line impurity detection that reduce both waste and re-processing. Every new run feeds back into our process analytics, letting us cut out inefficiencies and share operational improvements with partners right away. Whether adapting to new regulatory frameworks or transitioning to lower-carbon processes, our product line responds because our entire operation stays flexible with each customer demand, each feedback loop, and every new discovery at the bench.
Our time spent manufacturing and improving 2-Chloromethyl-4-Methoxy-3-Methylpyridine Hydrochloride shows that small choices in process design, quality checks, packaging, and real-world experience make the difference between commodity chemical and trusted specialty partner. Whether supporting rapid drug development, cutting-edge agrochemical innovation, or just-in-time supply across industries, we stand behind the advantages that come from years of direct production. Each drum and each pack carries the invisible labor of careful optimization. The molecule inside powers new ideas and processes, and our accumulated experience powers every batch.