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HS Code |
200635 |
| Chemical Name | 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride |
| Synonyms | 2,6-Dimethoxy-3,5-diaminopyridine dihydrochloride |
| Molecular Formula | C7H12Cl2N2O2 |
| Molecular Weight | 227.09 |
| Cas Number | 1026010-18-7 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water |
| Storage Conditions | Store at 2-8°C, protected from light |
| Purity | Typically >98% |
As an accredited 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride is supplied in a 10g amber glass bottle with a tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride: 8–10 metric tons, packed in safe, sealed fiber drums. |
| Shipping | 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride should be shipped in tightly sealed containers, protected from moisture and light. Package according to applicable hazardous material regulations. Use secondary containment and appropriate cushioning. Ensure clear labeling and include safety data sheets. Handle with care—avoid rough handling or exposure to incompatible materials during transit. |
| Storage | 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature or as specified on the manufacturer's label, ensuring that the material is clearly labeled and kept away from food and drink. |
| Shelf Life | 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride is stable for at least 2 years if stored cool, dry, and sealed. |
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Purity 98%: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride with purity 98% is used in pharmaceutical intermediate synthesis, where enhanced yield and product consistency are achieved. Melting Point 210°C: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride with melting point 210°C is used in high-temperature organic reactions, where thermal stability supports process reliability. Molecular Weight 248.12 g/mol: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride with molecular weight 248.12 g/mol is used in drug discovery assays, where precise molecular calculations enable accurate dosing. Moisture Content <0.5%: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride with moisture content less than 0.5% is used in fine chemical formulation, where controlled water content prevents unwanted side reactions. Particle Size <100 µm: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride with particle size below 100 µm is used in tablet manufacturing, where uniform blending and compaction are ensured. Stability Temperature up to 120°C: 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride stable up to 120°C is used in controlled release systems, where consistent performance over extended periods is achieved. |
Competitive 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride prices that fit your budget—flexible terms and customized quotes for every order.
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At our facility, 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride is not just another name on a catalog sheet. This specialty pyridine derivative holds particular importance for clients searching for high reactivity and purity in heterocyclic synthesis, advanced pharmaceutical work, or dye intermediates. Our development of this compound arises not from theoretical potential alone, but through years of effort focused on reproducibility, precise impurity control, and practical batch scalability. Satisfying strict end-user requirements always means committing to detail at the molecular level, and every step we take reflects the lessons learned from real production floors — not just lab benches.
We synthesize and purify the hydrochloride salt rather than supplying a free base because many downstream chemistries — including those in pharmaceutical and pigment manufacturing — demand the added stability, solubility, and predictable reactivity that salt forms provide. The dihydrochloride form resists degradation under ambient conditions and can be reliably weighed and dissolved, as opposed to the often more hygroscopic or oil-prone free base. Compound stability directly impacts operational efficiency in labs and plants. Our product comes as a crystalline powder, easy to handle and characterized using robust analytical routines, including HPLC and NMR, tied to industrial validation cycles instead of only academic protocol.
In the pyridine series, amine substitution patterns drive not just chemical reactivity, but compatibility with subsequent transformations — diazotization, reductive amination, or coupling steps, to name a few. The 2,6-dimethoxy substitution influences both electronic and steric profiles, altering the pushover of electrons within the ring while also modifying overall solubility. Synthetic groups choose this scaffold because it supports regioselectivity and unique cross-coupling routes. We have talked with formulators running into bottlenecks when using non-methoxylated or mono-methoxylated pyridinediamines, especially in the case of instability or limited solubility in common solvents like DMF, DMSO, or basic aqueous systems. These problems can cascade into low yields, troublesome purification, or unpredictable properties in final actives or pigments. Using our 2,6-dimethoxy product reduces these headaches from the outset.
We know from direct customer feedback that even minuscule shifts in residual moisture or trace metal content shift the reactivity of this salt. Researchers who moved onto kilogram-scale reductions or large-batch cross-couplings have reported that adapting protocols from free base or technical-grade dihydrochloride led to runaway side reactions or batch-to-batch drift. That is why our process control centers on reproducibility and a tightly defined impurity profile, established by not just routine spot samples, but by pulling parallel samples across entire lots.
Producing this compound at scale taught us repeatedly that balancing crystallization kinetics against haze formation and salt precipitation makes all the difference. Plant chemists struggling with materials from other sources have shared stories of clumpy, off-color, or deliquescent batches that force them back to square one, wasting both time and money. Through consistent agitation speeds, controlled cooling curves, and regular filter cake inspections, we achieve a reproducible, bright product that avoids those delays.
From our standpoint, reliability in physical form matters as much as purity. Pellet versus powder versus granule makes a world of difference to automated feeding or solution prep. Crystalline powder proves most versatile for both manual dosing and automated dispensing, minimizing dust and sticking. It also ensures efficient dissolution and easy characterization in downstream analytical steps. Receiving feedback directly from line chemists and formulators, we learned to avoid compressed or oversized agglomerates entirely — a lesson that only experience can drive home.
Our production batches operate within stringent purity windows, most commonly exceeding 99% by HPLC. The remaining impurity window includes tightly tracked levels of potential oxidized, dearylized, or ring-contracted pyridine byproducts, each of which can derail a complex synthetic step. We have invested early in residue profiling: ICP-OES monitors transition metal contamination during every run, particularly traces of copper, iron, or nickel — culprits that have ruined more than a few cross-coupling reactions downstream.
Water content does not receive a cursory glance either. A moisture window of under 0.5% (approaching 0.2% in most runs) sets our product apart from open-label offerings prone to atmospheric absorption. This matters for scale-up or synthesis in moisture-intolerant steps such as Grignard reactions, as even small upticks in hydration can change dye or drug intermediate color, crystallinity, or reactivity profile.
We compile a full suite of analytical data for each lot: melting point (for identity), microanalysis, chloride titration, and residual solvent analysis. Each data point comes from instruments calibrated and maintained to standards fit for regulatory audits. Producers downstream consistently encounter delays with less documented materials, spending days or weeks re-profiling new lots. Our clients report that with each batch, they see analytical consistency that translates into smoother project timelines and fewer failed runs.
Feedback from new pharmaceutical development has shown the value of high-purity 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride in building heterocyclic cores. Medchem teams seeking scaffolds for kinase inhibitor leads, antibiotics, or CNS-targeted actives have successfully deployed our product as a starting material, capitalizing on the dual electron-donating methoxy groups. These not only facilitate downstream functionalization — such as selective bromination or Suzuki coupling at specific ring positions — but also impart desired solubility for lead optimization work.
In pigment and dye work, process chemists report that our compound’s defined melting and consistent reactivity profile yield cleaner, brighter colors. Alternate pyridine diamine derivatives, even from reputable sources, often introduce variable shade, solubility, or process yield due to impurity creep. Several textile dye makers switching from traditional pyridine sources to our specification have reported fewer downstream purifications and batch reworks.
Our materials are also favored in specialty electronic applications — for instance, in the deposition of conductive polymer layers. Materials scientists explained to us that uncontrolled levels of ionic impurities disrupt desired layer morphology or impact surface resistance. Through careful chloride quantification and rigorous exclusion of nonvolatile metal ions, our salt translates to fewer device rejects or electrical inconsistencies.
Academic colleagues, engaged in ligand design or mechanistic studies, prefer the reproducibility in substitution calls permitted by this compound. We routinely field inquiries about non-standard ring-substituted pyridinediamines; most turn to 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride when other motifs fail due to solubility, sensitivity, or unpredictable ring activation. Having worked on grant-funded research ourselves, we recognize the frustration of batch drift and unexpected reactivity, and intentionally build that understanding into every batch.
Experienced buyers never judge just on price per kilo or “typical assay.” Most purchasing teams delve right into certificates of analysis, lot history, and even synthesis route. Organizing the upstream and downstream traceability of every batch gives procurement leads the confidence to integrate our salt into regulatory filings or validated processes. We document and archive full batch histories, so forensic tracebacks become possible even years later.
Some clients have come to us scarred by delays traced to offshore or anonymous makers — often flagged only after unexpected melting points, atypical odor, or color. While it seems basic, our focus on transparency and open communication closes the door on such mishaps. Each batch is both visually inspected and instrumentally validated, not just sampled “randomly.” Users comment on the difference in consistency and packaging — nothing leaks, no unexpected dust, and each container is traceable.
Teams scaling up from gram to multi-kilo orders report that this transition, so often fraught with obstacles, comes off smoothly when they can rely on identical handling properties and titratable performance over every batch. Differences in residual solvent or microstructure between lots can otherwise stymie early commercialization efforts. Only through years of working through supplier verifications and process adjustments do we realize how critical these small details become as projects scale.
Selecting 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride involves choices not just about purity, but about the real properties it brings to downstream chemistry. Many similar substrates are available in lower grades or as free bases — but these tend to pick up water, darken quickly, or fail to dissolve in key reaction solvents under scale-up. We’ve seen this play out in several customer pilot programs, where switching to a stabilized salt format allowed for longer bench stability and less stringent atmosphere control.
Compared to non-methoxylated pyridinediamines, this compound’s behavior offers key advantages for route design and output. Methoxy substitutions alter both nucleophilicity and coordination points, providing alternatives for selective substitutions or metal complexation. Colleagues working in ligand screen projects commented on the improved yields and selectivity they achieved after switching. Those using mixed-amino/methoxy pyridines note more frequent formation of byproduct tars and gums — likely related to mismatched electron densities and poor thermal control. Our regularly audited production parameters aim to eradicate such risks.
Some suppliers sell this salt with significant lot-to-lot drift — changes in water content, particle size, or even odor betray process inconsistencies or rushed drying. We retain product samples, monitor for stability over months, and spot-test each lot against internal benchmarks. Downtime for repurification, regrinding, or redrying vanishes with this level of oversight. Customers carrying out process validation runs for new drugs have told us that this unwavering quality is the key differentiator between “research only” chemicals and truly process-grade materials.
We draw our answers from years of producing difficult specialty heterocycles — not just from reading the literature. Reliable product quality starts with raw material vetting. Each precursor undergoes ID checks and bench validation before release, because impurities at this stage can be amplified by each synthetic sequence. On the floor, we take samples from every batch segment, not just the final drum, so variability within a production run won’t escape notice.
We built our purification and crystallization equipment specifically for water-sensitive salts and invested in climate-controlled packaging to stop product drift during long transits. Operators on our floor watch for early haze, particulate, or off-odors, rather than relying solely on end-point checks. Our lots regularly run through full analytical suites, traceable by lot to every timepoint, not just at shipping. This diligence means customers avoid the common headaches of batch failures, delayed process validations, or unpredictable project timelines.
We consult directly with labs and manufacturers deploying this chemistry, offering technical support and direct input on process tweaks — not generic “support lines.” Many partners face shifting regulatory hurdles, especially around solvent residues, trace metals, or documentation along the supply chain. Our direct handling of compliance, batch certification, and open data sharing saves time and cost, resulting in faster project launches and fewer regulatory setbacks.
Scaling up production without slipping on quality takes more than automated systems. Our teams manually inspect key process points — color change, moisture pickup, filter cake composition — because no single sensor can replace trained eyes. Routine operator meetings tighten up each process for the next cycle. Each production run ends with a review: what worked and what caused any variance. Improvements get put into effect rapidly, not weeks or months later.
Our commitment to this pyridine derivative runs through every level of production. Chemists who built our production campaigns remain involved with each lot, sharing troubleshooting ideas and supporting customer scale-ups. This tight feedback integration keeps our product quality not only where it should be, but always tuned to real-world outcomes.
Years of direct manufacturing experience inform our every tweak to process and packing. From optimizing crystal habit to monitoring trace contaminants, we know each challenge means higher performance in our customers’ applications. By continuously investing in equipment, training, and documentation, we aim to exceed the expectations of innovators relying on the finest specialty intermediates, not just chemical commodities.
Through every order of 3,5-Pyridinediamine, 2,6-dimethoxy-, dihydrochloride, we build on past learning to shape a better product — not just for our bottom line, but for the chemists, researchers, and manufacturers who make real-world impacts possible. Experience, care, and constant attention go into every batch. The results continue to speak for themselves, every step of the way.