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HS Code |
586450 |
| Iupac Name | 2-methyl[1,3]oxazolo[4,5-b]pyridine |
| Molecular Formula | C7H6N2O |
| Molecular Weight | 134.14 g/mol |
| Cas Number | 67484-27-5 |
| Appearance | Light yellow solid |
| Melting Point | 103-106 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=NC2=NC=CC=C2O1 |
| Inchi | InChI=1S/C7H6N2O/c1-5-9-7-6(10-5)3-2-4-8-7/h2-4H,1H3 |
| Pubchem Cid | 14815231 |
As an accredited 2-methyl[1,3]oxazolo[4,5-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a tamper-evident cap, labeled with chemical name, hazard symbols, and batch information. |
| Container Loading (20′ FCL) | 20′ FCL container holds 8 tons of 2-methyl[1,3]oxazolo[4,5-b]pyridine packed in 160 x 50-kg HDPE drums. |
| Shipping | 2-Methyl[1,3]oxazolo[4,5-b]pyridine should be shipped in tightly sealed containers, protected from light and moisture. Transport should comply with relevant chemical safety regulations. Package the compound with appropriate cushioning to prevent breakage, and clearly label for laboratory use. Consult the Safety Data Sheet (SDS) for any specific handling or hazard precautions during shipping. |
| Storage | 2-Methyl[1,3]oxazolo[4,5-b]pyridine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong acids or oxidizers. Keep the container tightly closed when not in use. Store in a designated chemical storage cabinet and ensure proper labeling. Use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | The shelf life of 2-methyl[1,3]oxazolo[4,5-b]pyridine is typically two years when stored in a cool, dry place. |
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Purity 98%: 2-methyl[1,3]oxazolo[4,5-b]pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical yield and low impurity levels are achieved. Melting point 175°C: 2-methyl[1,3]oxazolo[4,5-b]pyridine with a melting point of 175°C is used in high-temperature organic reactions, where robust thermal stability ensures reaction consistency. Molecular weight 136.13 g/mol: 2-methyl[1,3]oxazolo[4,5-b]pyridine of 136.13 g/mol molecular weight is used in medicinal chemistry for lead compound optimization, where precise mass contributes to accurate dosing. Particle size <10 μm: 2-methyl[1,3]oxazolo[4,5-b]pyridine with particle size below 10 μm is used in solid dosage form development, where enhanced dissolution rate improves bioavailability. Stability temperature 120°C: 2-methyl[1,3]oxazolo[4,5-b]pyridine stable up to 120°C is used in polymerization processes, where it maintains reactivity without degradation. HPLC grade: 2-methyl[1,3]oxazolo[4,5-b]pyridine of HPLC grade is used in analytical reference standards, where accurate chromatographic quantification is required. Water solubility <0.1 g/L: 2-methyl[1,3]oxazolo[4,5-b]pyridine with water solubility less than 0.1 g/L is used in organic solvent-based formulations, where low aqueous solubility enhances chemical compatibility. |
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Customers often ask what separates one fine chemical from another. In the manufacturing plant, those differences emerge clearly as we guide every batch from the first charging of raw material to the final pass through quality analysis. 2-Methyl[1,3]oxazolo[4,5-b]pyridine comes up often in conversations about innovative heterocycle chemistry, especially for researchers searching for distinct electronic properties and structural features. Years of experience refining its synthesis under real-world conditions have shown where this compound excels—and where extra care delivers higher value to scientists and formulators.
Lab jargon and marketing lingo often paint blandly similar portraits of specialty heterocycles. On the factory floor, we’re focused on details that matter directly to users—crystal form, purity, trace metal content, and actual reproducibility from gram to hundred-kilo scale. Each batch of 2-methyl[1,3]oxazolo[4,5-b]pyridine undergoes HPLC and NMR characterization. Skilled chemists monitor color, odor, melting point, and residual solvent, because any oddity affects downstream reactions.
Our direct production process skips multi-step work-up typical of outsourced traders. By streamlining distillation, filtration, and crystallization to tighter timeframes, we reach above 99% purity without leaving behind stubborn byproducts. This extra fraction of purity may sound incremental, but experience in medicinal chemistry tells us that undetectable contaminants sometimes cripple a project much further down the line, especially as compounds move into more sensitive screening.
There is little substitute for direct control over every variable that shapes a final molecule. We choose raw methylpyridine and glycine derivatives based on years of observed reactivity and have modified reactor protocols to resist charring, protect product from oxygen exposure, and guard against batch-to-batch drift. Researchers often comment that our crystalline lots dissolve more cleanly in DMSO and MeOH—signs of real consistency, not just paperwork compliance.
In pharmaceutical and agrochemical discovery, a tightly-defined impurity profile isn’t just a documentation formality. Even minor peaks caused by degraded solvent residues or metal catalysis can cause headaches in scale-up. Our technicians calibrate each process stage against internal chronologies of successful and marginal runs, so those trace signals are flagged and traced to their root. It’s a hands-on approach honed by repeated cycles of success and failure under the raw light of practical industrial production.
Early in our journey with 2-methyl[1,3]oxazolo[4,5-b]pyridine, we learned that its utility emerges most in niches where both reactivity and selectivity have to walk a fine ridge. Colleagues in analytical method development praise its rigid heterocyclic backbone for acting as a reference standard, particularly within HPLC method validation regimes. In medicinal chemistry, its nitrogen-rich framework lends itself to SAR exploration, enabling design teams to build libraries aimed at kinase, GPCR, and ion channel targets where small changes cascade into large shifts in biological response.
Customers developing next-generation electronics materials have recently tapped our product to exploit its unique π-system, which slots smoothly into conjugated structures for organic semiconductors or OLED components. Having direct feedback from those working at the design and application stage lets us tune drying, particle size, or shipment packing, ensuring what leaves our warehouse lands in their procedures without disrupting delicate synthetic sequences.
Over the years, we’ve seen a spectrum of production philosophies. Some suppliers chase yield-to-cost metrics by shortcutting purification or by blending lower-spec materials. Our plant resists this pressure by investing in final-stage polishing that strips out faint yellow tint and off-odors— because most of these traces creep in from heat exposure or unmonitored hydrogen atmosphere. This care may dent short-term throughput, yet our partners in drug discovery and high-precision analytical labs confirm that those invisible extras become visible in project outcomes.
It’s tempting to assume that two samples registering as >98% (HPLC) will behave the same way. Those small slivers of unknown constitute the difference between advancing a lead series versus chasing faulty spectra or seeing unexplained cell cytotoxicity. From our end, routine elemental analysis, water determination, and per-lot certificate provision give our customers back precious hours they would waste troubleshooting ambiguous reagents.
Sustainability conversations often feel remote from day-to-day plant operations. That said, actual chemical production forces real change by necessity. Our team has reworked solvent recovery systems for greener, closed-loop operations. By optimizing each reflux and limiting reagent push, we cut per-lot waste and reduce environmental load—long before any formal green chemistry audit. These process updates weren’t top-down dictates, but arose through weekly operator meetings in response to what we learned tackling bottlenecks, gummed filters, and batch upsets in practice.
For our region, environmental discharge from fine chemical production matters. With more attention on water management and waste stream monitoring, local regulatory teams have made direct site visits part of their routine. Our plant invested early in online TOC and pH monitoring, not from compliance alone, but because consistent output demands stable local conditions. With cleaner water leaving our boundary, we maintain not just our own license but the future viability of jobs, families, and the broader ecosystem around us.
Every seasoned chemical manufacturer accumulates a “mental logbook” of near misses and breakdowns that shape later protocols. Early trials on 2-methyl[1,3]oxazolo[4,5-b]pyridine taught us to respect the batch time curve; cut corners, and we saw off-colors, sticky cakes, and spontaneous decompositions. Once, a slightly off-ratio catalyst led to split-stage precipitation, clogging downstream purification and wasting hours under emergency flush. Another run, water ingress from an aging pipe spiked hydrolysis byproducts across several batches.
Embedding lessons from these missteps, we enforce robust incoming goods checks, double-confirm ratios before every charge, and track process steps electronically. Our continuous batch records and in-process pulls shift reaction management from blind hope to active intervention. Operators rotate across stations, building task redundancy and a feedback culture that rewards careful observation. Most solutions point to basic truths: inspect seals, verify solvent, monitor temperature and pH obsessively. The gap between routine and disaster can be very slim in specialty organics—we do our utmost to keep to the right side of that line.
Some of our most satisfying project outcomes come from direct exchanges between our chemists and end users on the lab bench or in front of a computer screen. INA pharmaceutical client shared that their screening cascade benefited from our lot-to-lot product uniformity; by eliminating batch-dependent surprises, their data pipeline ran weeks faster. Academic groups looking to publish on new synthetic routes reach out for extra spectral verification and stability tracking. Instead of shrugging off these requests, our technical team enjoys the dialogue because it sharpens our focus on what really counts.
Supporting users doesn’t require flashy branding or excessive paperwork. Through routine tech support calls and shared analysis, our clients gain access to the “fingerprint” of each lot. Efforts like custom vial sizing, just-in-time shipment, and post-delivery tracking create a network of trust. By keeping these channels open, we foster a scientific community that extends beyond any one batch or research cycle.
Markets evolve, and so do molecular design targets. Years ago, 2-methyl[1,3]oxazolo[4,5-b]pyridine appeared rarely outside academic journals; today, multidisciplinary teams ask for more—tighter particle control, UV-Vis transparency, or avoidance of specific halides. Reactivity patterns matter more as chemical biology and electronics fields blend. We hear that even trace metals can provoke functional drop-off in biosensor arrays or enzyme assays, so our analytical range expands yearly to respond.
We don’t just wait for formal complaints. Through routine scanning of the open literature and site visits to leading research parks, our R&D group feeds back emerging purity or solubility targets to synthesis and QC. If a new grade improves yield or reproducibility, operations pivot to prove those conditions consistently across scales. In competitive fields—from fragment-based screening to smart polymer synthesis—minor differences accumulate big impact.
Too many chemical product introductions sound interchangeable. In the real economy of research and manufacturing, small differences compound. 2-Methyl[1,3]oxazolo[4,5-b]pyridine occupies a narrow, but significant slot in modern synthetic chemistry. Its rigid, aromatic structure opens the door to new analogs that challenge traditional medicinal motifs, catalyze novel conjugations, or anchor photophysical studies. Users who rely only on catalog data risk missing both challenges and opportunities that come with real-world material.
On our production line, sweating the last decimals of purity and controlling lot history deliver not just compliance, but usable results. By focusing on what moves a reaction forward—or prevents unnecessary troubleshooting—we support scientists racing difficult deadlines and companies pushing to publish or patent before competitors. The value multiplies for those trying to translate a single compound from microgram discovery to kilogram pilot or clinical scale.
Customers judge manufacturers by more than certificate values or the just-in-time arrival of jars and drums. Our reputation as a producer of 2-methyl[1,3]oxazolo[4,5-b]pyridine depends both on technical execution and straightforward, timely communication. We maintain open feedback channels so users alert us quickly to any issues—sediment, color shift, label ambiguity. This dialogue helps us improve after every misstep or suggestion.
Direct relationships with researchers, procurement officers, regulatory managers, and even project sponsors form a practical network that steers product improvements. Regulatory changes happen fast. By keeping our compliance documentation current and transparent, we lower the risk of shipment holds or new analysis demands disrupting downstream projects. Our QA team adapts suite documentation to reflect shifts in EU, US, or Asian regulatory priorities.
Building trust batch by batch outcomes through decades of combined hands-on plant experience. Our teams take pride in their craft, knowing well that cutting a corner for one batch could undermine years of partnership.
Challenges always arise—unexpected precipitation, delayed shipments, changing regulatory cut-offs, or custom grade requests. Factory teams tackle these issues head-on, collaborating with technical groups and logistics partners to find workable solutions. Once, when a top client asked for water content lower than our standard spec to suit a sensitive organometallic application, we adjusted atmosphere and drying time, then provided side-by-side batches for comparison. The project advanced, and our process improved for all future lots.
Clear procedures, accountability, and relentless attention to feedback shape continuous improvement. We see each hurdle not as a setback, but as a lesson in how to serve a broad, evolving slate of scientific partners. By resisting one-size-fits-all approaches, our team ensures flexible delivery—from bulk drum to custom micro-jar—matched to exactly what the research or production context calls for.
Making 2-methyl[1,3]oxazolo[4,5-b]pyridine isn’t simply about uploading another SKU to an online catalog. Every stage from raw sourcing to product packing, labeling, and final QC is done with an eye toward the consequences—not just for the compound, but for real-world progress in pharmaceuticals, diagnostics, functional materials, and academic research. Consistency in output signals not just technical excellence, but a duty to the finished project, the downstream application, and ultimately the patient or consumer at the end of the chain.
We owe our reliability to a combination of technical acumen, direct user feedback, and a willingness to own and fix problems that some might ignore. For customers, this translates to measured confidence in each bottle, a direct handshake with our process, and open lines to troubleshoot, adapt, and innovate together.
Users of our 2-methyl[1,3]oxazolo[4,5-b]pyridine benefit from knowing every run is managed with practical vigilance, backed by staff who take satisfaction from solving practical problems rather than reciting claims. Working this way isn’t always easy, but it drives real results and lasting partnerships.