|
HS Code |
632009 |
| Chemical Name | 3,4-Dimethoxy-2-Pyridinemethanol |
| Molecular Formula | C8H11NO3 |
| Molecular Weight | 169.18 g/mol |
| Cas Number | 74630-71-2 |
| Appearance | White to off-white solid |
| Melting Point | 76-80°C |
| Solubility | Soluble in DMSO and methanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Smiles | COC1=C(C(=NC=C1)CO)OC |
| Inchi | InChI=1S/C8H11NO3/c1-11-7-4-3-9-8(5-10)6(7)12-2/h3-4,10H,5H2,1-2H3 |
As an accredited 3,4-Dimethoxy-2-Pyridinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25g of 3,4-Dimethoxy-2-Pyridinemethanol, sealed with a screw cap, labeled with hazard and product details. |
| Shipping | **Shipping Description for 3,4-Dimethoxy-2-Pyridinemethanol:** This chemical is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported as per applicable regulations for laboratory chemicals, ensuring safety and integrity. Temperature and handling instructions are included, and all packages are properly labeled with hazard identification and documentation for compliant shipping. |
| Storage | 3,4-Dimethoxy-2-pyridinemethanol should be stored in a tightly sealed container, kept in a cool, dry, well-ventilated area away from sources of ignition, heat, and direct sunlight. Store away from incompatible substances such as strong oxidizing agents and acids. Ensure appropriate labeling and access only to trained personnel. Avoid contact with moisture and tightly close the container after each use. |
Applications of 3,4-Dimethoxy-2-Pyridinemethanol in Industrial ManufacturingAs a direct manufacturer of 3,4-Dimethoxy-2-Pyridinemethanol, we support large-scale producers across multiple industry segments where this advanced intermediate enables targeted and efficient synthesis workflows. The following application scenarios describe proven, real-world integration within demanding production environments. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisAPI manufacturers utilize 3,4-Dimethoxy-2-Pyridinemethanol as a key intermediate during stepwise heterocycle construction for central nervous system and oncology drug candidates. Its pyridine backbone and functionalized methoxy groups facilitate selective functional group transformations under established reaction conditions, improving both step economy and product purity. The intermediate typically enters multi-stage batch synthesis lines, where its controlled addition within specified molar ratios supports strict process validation and scalable GMP compliance for regulated pharmaceutical output. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Crop Protection Active Ingredient ManufacturingAgrochemical formulators depend on 3,4-Dimethoxy-2-Pyridinemethanol as a pyridine-based building block during the synthesis of certain herbicide and fungicide actives, where its electronic properties promote targeted substitution and cyclization reactions. Typical use occurs in closed-system multi-step syntheses, governed by crop protection regulatory requirements, with analytical controls at each stage to assure batch consistency and traceability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Material Coatings and Electronics ChemicalsIn electronic component and advanced functional coatings production, process engineers select 3,4-Dimethoxy-2-Pyridinemethanol as a precursor for specialty pyridine-containing binders and electron-transporting monomers. Its consistent purity and reactivity enable precision polymerization in electronics-grade resins, while stringent quality systems ensure trace-metal and moisture limits suitable for microfabrication processes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical & Specialty Chemical SynthesisProducers of fine chemicals and specialty intermediates employ 3,4-Dimethoxy-2-Pyridinemethanol for selective construction of N-heterocycles, targeting use in fragrance, flavor, and dye precursor lines. Its controlled reactivity offers advantages for regioselective formylation, alkylation, or C–N coupling under mild conditions. Quality assurance protocols maintain transparency and reproducibility from analytical scale through commercial production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,4-Dimethoxy-2-Pyridinemethanol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In the line of fine chemical production, 3,4-Dimethoxy-2-pyridinemethanol emerges as a selective and versatile intermediate. Over our years in the plant, we've handled the manufacture of this compound at both pilot and commercial scale, watching the science and demand evolve. Unlike simple pyridine derivatives, the presence of the methoxy groups at the 3 and 4 positions, coupled with the hydroxymethyl side chain, gives this molecule an edge in reactivity and solubility that makes it particularly attractive under specific synthesis routes.
For many in the field, the true value of 3,4-Dimethoxy-2-pyridinemethanol lies in its role as a cornerstone for downstream products, especially in pharmaceutical and agricultural synthesis. Lab teams reach for it because it offers a unique scaffold—particularly for compounds targeting central nervous system pathways or certain crop protection agents. We've observed formulators and researchers request this exact substitution pattern to reach properties not possible by simply methylating or modifying other sites on the pyridine ring.
On a practical level, working with this molecule gives access to synthetic flexibility. Chemists capitalize on the electron-donating nature of the methoxy groups to drive reactions toward desired regioselectivity, while the alcohol group allows for further modification such as esterification or etherification without much difficulty. These traits help streamline steps, cut down purification cycles, and reduce total process time, which directly benefits both bench-scale research and industrial throughput.
Our production facility synthesizes 3,4-Dimethoxy-2-pyridinemethanol by carefully controlling the methoxylation and side-chain introduction steps. Batch logs show that the typical output appears as an off-white solid, sometimes tending towards pale yellow if traces of precursor remain post-crystallization. Our primary focus is delivering a product with purity above 98%, determined by HPLC and supported by GC-MS as needed for customer assurance.
Moisture content often stays below 0.5%, thanks to our vacuum drying process, which directly addresses issues of batch stickiness and potential clumping during storage. Anyone who has handled lower-purity grades would recognize the problems that arise when water or by-product salts remain post-reaction; these can trigger side reactions in sensitive synthesis and throw off precise stoichiometry. By sticking to tight process controls, we support more reproducible results for users on the receiving end.
Our technical reports document that the melting point typically falls in the 75-80°C range. This manageable melting point supports solid feeding during large-scale processing and contrasts sharply with analogs that melt at much lower, more finicky temperatures, which complicates dosing and transfer. Our choice to package the product in moisture-barrier lined drums directly responds to feedback from repeat users who store inventory for extended periods.
The chemical market offers a spectrum of pyridine-based compounds, but 3,4-Dimethoxy-2-pyridinemethanol occupies a distinctive niche. Chemically, the dual methoxy substitution at those particular ring positions drives both physical and chemical behaviors that differ from, say, 2-methoxy or non-hydroxymethyl pyridines.
Our process chemists note that the 3,4-dimethoxy pattern adjusts electron density in a way that stabilizes intermediates during coupling reactions or nucleophilic attacks. This allows downstream modifications over a wider range of pH, which opens possibilities beyond what 3-methoxy-4-hydroxy or unsubstituted pyridines allow. In one collaboration, a pharma partner achieved notably higher yields in Suzuki couplings compared with other pyridine alcohols, attributing this to improved precursor solubility and better compatibility with their palladium catalysts.
On the formulation front, end-users have described easier crystallization and more predictable solid-state behavior compared with more volatile or less substituted variants. Anyone running kiloliter reactors knows the pain of handling intermediates that form sticky oils or amorphous gums. Our batches of 3,4-Dimethoxy-2-pyridinemethanol remain free-flowing and uniform—key for automated feeding and minimized cleaning downtime.
Shelf-life ranks high among customer concerns, especially when warehousing for multiple product cycles. Unlike many hydroxymethyl pyridines that tend to darken or decompose, our material stays stable under proper storage, owing to that methoxy shielding. Real-world inventory checks months after receipt show minimal color shift or degradation—a fact technicians on site have repeatedly documented and appreciate.
Feedback from our partners paints a clear picture: this compound’s structure is tailor-made for intermediate roles in API development and specialized agricultural chemicals. Several projects in central nervous system drug pipelines rely on the clean introduction of a substituted pyridine core, where this alcohol serves as a direct precursor for further oxidation or as a handle for selective attachment to more complex frameworks.
In certain agrochemical syntheses, 3,4-Dimethoxy-2-pyridinemethanol works as a building block for heterocyclic synthons that resist photodegradation, extending field stability of the final product. Formulators appreciate that the relatively high melting point and low volatility allow safe storage and straightforward transport compared with more sensitive analogs.
Real lab notes reflect the time saved during purification. Post-reaction work-ups with our product often involve simple filtration or crystallization, reducing reliance on chromatography—an advantage both for R&D and for those ramping up to production scale. Each hour not spent recleaning columns, reactors, or pipelines translates directly into higher throughput and lower costs.
There’s also the matter of analytical clarity. Our QC lab monitors each batch to ensure a consistently narrow HPLC chromatogram profile, giving users confidence during incoming inspection. End-users working in regulated environments have shared that our clear set of paperwork—supported by COAs and batch histories—is a direct asset during audits or process reviews.
Those who’ve navigated the specialty chemical market know the difficulties in finding reliable sources for advanced intermediates. Supply chain disruptions, fluctuating precursor availability, and inconsistent purity all plague manufacturers. We focus on building transparent supply contracts for the raw materials critical to this synthesis, aiming to keep availability high and price variance low.
On the plant floor, our process teams adjust reactor conditions dynamically in response to minor variations in raw material quality. By running side-by-side small-scale verifications before scaling, we prevent costly mistakes that can result from subtle impurity carryover.
We’ve encountered issues in the past where upstream suppliers switched solvent grades or altered storage temperatures, leading to unexpected outcomes during the methoxylation stage. Our response included bringing analytical support further upstream—running GC and NMR checks not just on final product but on incoming agents. This hands-on oversight directly improves final yield, and we've documented fewer customer complaints since making these changes.
Transportation poses a separate challenge, particularly in humid climates. Our logistical teams shifted to using desiccant bags and reinforced drum liners based on user reports of caking or moisture pickup. Those tweaks now mean less product loss and hassle at the receiving warehouse.
Most chemists know that handling pyridine derivatives can raise unique safety concerns, especially when working at scale. 3,4-Dimethoxy-2-pyridinemethanol does not carry over the strong odors or acute toxicity of unsubstituted pyridines, but powder control and minimal skin/eye exposure still remain good practice in any equipped facility. In our plant, we rely on standard PPE and enclosed feeding systems to cut down respirable dust, and our spill logs remain minimal as a result of this configuration.
Our process teams maintain a robust review cycle of all incidents, minor and major, with constant refreshers on safe handling and waste disposal. Waste streams containing methoxy pyridine residues go directly into distillation or approved disposal, and we continue to monitor stack emissions to assure compliance. User trust stems from more than a documented MSDS—it comes from steady, visible investment in workplace safety and environmental compliance. Our approach is to treat every batch with the respect due a potentially hazardous substance, irrespective of how mild it may seem in routine handling.
We treat QC as an ongoing process, not just a bottleneck at dispatch. Each lot runs through a sequence of physical inspection, chromatographic assessment, and moisture analysis. If any parameter drifts outside our target range, that lot gets flagged and reworked or rejected according to internal protocol. This hands-on approach differs from more hands-off distribution models, where traceability can blur across long supply chains.
Our site’s QA team works shoulder-to-shoulder with production—not in a separate office—so feedback on off-spec product cycles swiftly back into process adjustments. We also conduct random stability checks on retained sample jars to validate shelf-life claims, sharing real data when users request details for regulatory submissions.
Customers in regulated fields, such as pharmaceuticals, emphasize the growing need for clean audit trails. Our batch records stay accessible for multiple years, and anyone needing deeper technical information—such as residual solvent levels or confirmation of low heavy metal content—can count on us to deliver new sets of analytical certificates on request, not just with the initial consignment.
Over time, we have tracked a steady evolution in the applications for 3,4-Dimethoxy-2-pyridinemethanol. Researchers are seeking out this compound for newer types of coupling reactions, bioconjugation work, and as a probe in complex molecular scaffolds. Our commitment has been to support these innovators not just by steady supply, but by offering small pilot lots for experimental runs—sometimes tweaking process parameters to produce custom grades with alternate particle size or higher purity.
We also receive requests for documentation clarifying absence of animal-derived substances, residual solvents, or certain elemental impurities—usually triggered by emerging regulatory trends or concerns about contamination. Each of these requests feeds back into our process, spurring real improvements in how we manufacture, test, and package the compound.
One new direction involves working with collaborative clients to minimize solvent usage during synthesis, aiming for greener, less hazardous process waste. Results show a reduction in both footprint and cost, which appeals to partners prioritizing compliance with environmental standards such as REACH or local green chemistry initiatives.
What stands out most over years of supply is the feedback from those at the lab bench and the production line. Process teams and formulators appreciate knowing exactly what they're getting in terms of batch consistency, real-world handling, and technical support. Academic groups developing novel molecules or process chemists looking to scale up from grams to tons share similar priorities: security of supply, batch-to-batch predictability, and the basic confidence that every shipment matches expectations.
Many customers have described their relief after switching to material that meets tight control standards, reflecting reduced troubleshooting downstream and less time wasted tracking down the source of random yield losses. Orders come in from places where slightly different pyridine derivatives simply won't work—sometimes due to nuanced electronic effects, other times due to regulatory restrictions on process impurities. Our role remains to bridge that gap between raw chemistry and reliable, usable material.
For those working in regulated markets, documentation and traceability are as important as product itself. Our system holds back-samples from every batch, links them to digital records, and backs up all analytical data—ready for review during any process change or inspection. Multiple users have relied on these archives during regulatory agency audits, passing with no deficiencies cited on material consistency or traceability.
No chemical supply is entirely immune to disruption, but our aim is to buffer customers against market shocks and quality slips wherever possible. In the past, supply interruptions for key intermediates have posed problems, but by investing in forward stockpiling and multiple-source contracts with upstream vendors, we improve continuity for critical end-users. Production schedules now run on a combination of real-time inventory tracking and predictive planning, so when demand unexpectedly surges, plant capacity can flex up.
Quality drift presents a separate challenge, especially over long production runs. Our continuous sampling program catches subtle changes early, whether they're related to new raw material batches or seasonal shifts in process water quality. Factory upgrades to filtration and drying keep physical specifications tight, and customer call-ins for custom grade adjustment feed directly into the plant’s workflow.
Manufacturing 3,4-Dimethoxy-2-pyridinemethanol is more than a synthesis run; it’s about responding directly to what users require on the ground. Our technical support comes from the same chemists and operators responsible for making, testing, and handling the material—so advice given is practical and based on hard-earned knowledge. Questions about reactivity, storage, or compatibility get real answers grounded in our actual experience, not broad generalities.
End-users also drive much of our process improvement: every challenge brought to us—a sticky batch, a trace contaminant, a puzzling analytical discrepancy—generates a cycle of troubleshooting that feeds back into advance planning and next-batch quality. This approach keeps waste low and improvement ongoing.
From our manufacturing vantage point, 3,4-Dimethoxy-2-Pyridinemethanol is likely to persist as a specialty niche product because of the deliberate, tailored uses driven by its structure. The steady growth in both pharma and agrochemical innovation ensures a continuing market, especially among those unable to substitute with cheaper but less suitable alternatives. Purely commoditized chemistry rarely offers the same reliability, and for critical syntheses, customers are asking for quality and documentation rather than minimum price.
We remain invested in ongoing improvement—finer analytical protocols, lower impurity thresholds, more sustainable process options, and closer customer dialogue. This approach ensures those using this compound enjoy results that support not just lab-scale discovery, but also full production scale-up and regulatory approval.