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HS Code |
526366 |
| Chemical Name | 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine |
| Molecular Formula | C14H18N2O |
| Molecular Weight | 230.31 g/mol |
| Cas Number | 1652236-46-4 |
| Appearance | White to off-white solid |
| Smiles | CC(C)C(=O)c1ccn2c(c1)cnc2C(C)C |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Synonyms | No widely known synonyms |
| Inchi | InChI=1S/C14H18N2O/c1-9(2)13(17)11-6-7-16-12(8-11)10(3)15-14(16)4/h6-10H,1-5H3 |
As an accredited 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, sealed with a PTFE-lined cap, labeled with chemical name, formula, CAS, and hazard symbols. |
| Container Loading (20′ FCL) | 20′ FCL (Container Loading) for 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine ensures secure bulk transport, minimizing contamination and moisture exposure. |
| Shipping | The chemical **2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine** is shipped in tightly sealed glass containers, protected from moisture and light. It is packaged according to regulations for laboratory chemicals, typically under ambient temperature unless otherwise specified. Shipping is handled by certified carriers, following relevant safety and hazardous material transport guidelines. |
| Storage | 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine should be stored in a tightly sealed container, protected from light and moisture. Store at room temperature (15–25°C) in a well-ventilated, dry area, away from incompatible substances such as strong oxidizers. Handle under an inert atmosphere if recommended, and ensure proper labeling. Keep out of reach of unauthorized personnel and follow local chemical safety regulations. |
| Shelf Life | 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine has a typical shelf life of 2 years when stored in a cool, dry place. |
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Purity 98%: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistency in target compound production. Melting Point 142°C: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine with a melting point of 142°C is used in solid-form formulation processes, where its thermal stability enhances product quality. Molecular Weight 245.32 g/mol: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine of molecular weight 245.32 g/mol is utilized in medicinal chemistry research, where accurate dosing and reactivity are critical for reproducibility. Particle Size <10 μm: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine with particle size below 10 μm is used in tablet manufacturing, where it improves dissolution rate and bioavailability. Stability Temperature up to 125°C: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine stable up to 125°C is applied in reactive process development, where it maintains structural integrity under heat. HPLC Assay ≥98%: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine with HPLC assay ≥98% is used in quality-controlled laboratory analysis, where it guarantees reliable analytical performance. Moisture Content <0.5%: 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine with moisture content less than 0.5% is utilized in lyophilized drug development, where low water content preserves compound stability. |
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Every chemical tells a story woven from deliberate choices and precise execution. Our journey with 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine begins on our own line, where the focus runs deep into reaction control and attention to detail. The nature of heterocyclic compounds demands far more than textbook chemistry. We leaned into over a decade of process improvements, pushing for clear streams, reproducible batches and enough flexibility to match end-use needs in pharmaceuticals and specialty applications. Over the years, we saw how tweaks in purification or crystallization impact downstream results—right from purity profiles to difficult-to-trace impurities. Our team shapes product quality by starting with founders’ hands-on approach: test every batch, review every anomaly, never settle for near enough. It's not just another acronym or obscure molecule here; it's the outcome of our sweat and expertise poured into reactors we calibrate daily.
Labs come to us looking for this compound when stringent structure and purity take center stage. Its unique scaffold lends itself to targeted pharmaceutical research and the early stages of custom synthesis for new therapeutic candidates. The compact, fused heterocycle and specific substituents sharpen its profile for medicinal chemistry, standing apart from similar pyrazolopyridines. Our in-house chemists tracked market chatter for shortcuts and knock-offs — cuts in corners show up rapidly under NMR and HPLC, so we designed controls at each process step, not just at final testing.
Through feedback from formulation scientists, we realized even minor deviations in isobutyryl group ratios skew performance in SAR studies. Some teams ask for micron differences in crystal size or solvent residue thresholds. We worked through surface-level challenges and into the heart of molecular batch integrity. So yes—what makes our material valuable isn’t just cost or paperwork, but years of trial, error, and listening to scientists demanding exactly what works at their bench.
Every kilogram that leaves our warehouse sees the same care. For new customers, it may seem granular, but technicians here understand what a persistent trace of unreacted pyrazole can do in sensitive biological assays. We follow multi-stage purification, then run targeted impurity profiling for both known and unsought contaminants. This led us to fine-tune solvent mixtures and even adjust distillation rates seasonally, based on our factory’s local climate swing. Experience keeps us attuned to changes—a slight shift in tank temperature or a new lot of upstream solvent triggers a roundtable review, not a blind pass.
We don’t hide behind blanket statements about “high purity” or “industry standards;” real output matters, and verification beats slogans every time. Our batches exceed 98% purity by GC and pass all visual and tactile inspections because we treat the end result like something we’d trust in our own project work. Packing, too, demands vigilance. Some solvents leach tiny amounts of reactants; we switched to lined containers and sealed units after clients found micro-particle inconsistencies on other suppliers’ shipments.
This molecule’s blend of isopropyl and isobutyryl substituents sits at a crossroads for reactivity—those who synthesize related compounds know it well. Many in our field assume that once a pyrazolopyridine core is built, the subtleties look after themselves. We learned on the floor that starting materials never behave identically; freshness and storage history change outcomes in real life, making oversight on each step crucial. For batches running above the half-ton scale, one missed parameter in stirring speed or temperature profile shows up at the analytical bench.
Technicians have direct experience spotting shift—either by smell, flow property, or UV trace. Over time, we introduced layered QC: analysts in different buildings re-confirm key metrics, not just automated samplers. We standardize reference material and retain portions from every run for back-checking. The team swapped tales of discovering why a certain batch dissolved too slowly, only to find that a supplier had tweaked a distillation column plate. We built a protocol for mandatory supplier re-testing in-house to stop that from repeating.
What separates this compound from lower-cost analogues or mass-market pyrazolopyridine bases lies in two connected areas: chemical precision and process consistency. The isopropyl/isobutyryl combination offers specific steric profiles, relevant for researchers working to build out new analogues of kinase inhibitors, antivirals, or CNS agents. We’ve tracked requests for “near neighbors” and seen disappointment shared by scientists who tried less curated samples.
A number of market competitors pull shortcuts for scale or cost: skipping a chromatographic step, trading off a bit of yellow tint, or letting in 1% side-products since “it doesn’t matter for synthesis.” Over hundreds of feedback cycles, our team chased down what actually happened in clients’ hands: reaction failures, non-reproducible screens, and costly loss-of-time. One chemist reported that even ppm-level cross-contaminants changed assay windows; our response was to double analytic cross-checks and set internal spec limits tighter than most published protocols.
Enthusiastic operations focus not just on cleaning up after mistakes, but on predicting them. Technologists on our line debated granularity versus flowability until production and formulation units met to redesign our drying cycle. The result: less caking, more direct weighing into client vessels, and fewer re-drying steps for downstream labs. Some colleagues remember a year we faced a shortage of a specialty drying agent; instead of outsourcing or cutting corners, we sent samples for collaborative testing, eventually investing in a new on-site drying suite.
Much of the industry hears “new intermediate” and thinks of catalog sheets or vague promises. We know most buyers for this compound don’t want a static sample—they rely on dependable scale-ups for active pharmaceutical ingredients, advanced intermediates, and performance-driven research. This molecule rarely sits idle; it moves quickly into combinatorial chemistry, lead optimization, specialty ligands, or libraries targeting untapped pathways.
We didn’t stop at serving catalog needs. Over time, our real-world partners sent us insight from trial runs and scale-up hurdles. In pilot processes, a subtle difference in melting point sometimes threw off yield balances or generated unexpected byproducts. Those lessons pushed us to dial in batch process controls for tighter thermal and purity bands. We value that customers return with specifics: details about reactivity, color stability, or even shipping humidity. Our job remains satisfying those constraints, not just because we state a generic quality promise.
Feedback isn’t one-way. Early customers wanted only small research samples; later, pilot teams wanted multi-kilo lots with explicit impurity profiling. Most recently, requests arrived from groups validating new patent-protected syntheses, seeking both reliability and discretion. In each case, our operations flexed—smaller vacuum-dried vials or larger drums with tamper-proof linings—to reflect those evolving needs.
We keep hearing stories of scientists frustrated by tiny differences between suppliers. The truth stands: two bottles bearing the same name may behave far apart in a synthesis. The “feel” of a high-integrity sample—correct color, immediate dissolution, and total fit with prior batch data—justifies every hour we spend honing our procedures. Our in-house team stands by every lot, not through slogans, but through direct, day-to-day observation, deeply rooted in small but crucial choices.
Many manufacturers gloss over these realities. By contrast, we respond in real time. If a customer in Europe notes a change in particle size month to month, we pull records, re-validate, and consult our technical staff. Even a modest switch in container seal integrity led us to adopt multi-layer barriers and desiccant shrouds. These changes do not happen on paper—they emerge from hands-on trials and internal discussions, always aimed at removing frustration from the scientist’s workflow.
As a manufacturer driven by solving hands-on problems, we see ourselves not as distant suppliers, but as part of the experimental chain. This compound reflects our core strengths: adaptability, technical tenacity, and open doors for feedback. Reports of field issues never go to waste—they fuel new trials, push us toward cleaner cuts, and set new in-house rules for what defines acceptable quality.
We never view our job as complete. The landscape for advanced heterocycles remains dynamic, shaped by both foundational research and shifting regulatory demands. Our plan involves keeping capacity ready for upscaling, holding reserves against supply chain shocks, and building closer ties with upstream and downstream specialists. Each innovation, whether it’s a purification tweak or improved packaging, is grounded in direct experiences with what makes a difference at the lab bench and in production vessels.
Quality systems live and breathe here. We keep analytical labs close to the main lines so that delays don't break our feedback circuits. Our teams conduct regular internal audits, accountability checks, and invest in new detection hardware—as small as microbalances and as large as full-spectrum NMR for on-site confirmation. Staff meet not only to review deviations but to brainstorm what smaller, subtler changes might keep our product ahead of unpredictable trends.
We build our process controls and batch tracking around visibility. Everything we produce pairs with digital records, unique traceability, and open records for client verification upon request. Our operation welcomes third-party audits and has built partnerships with university labs to routinely pressure-test our output.
Responsible chemical manufacturing today means watching inputs, by-products, and the environmental profile at every turn. We looked closely at how each new method, solvent, or raw material choice aligns with both performance and broader sustainability targets. Waste minimization plans cut thousands of liters of solvent per year. Routine reviews of effluent and solid by-product treatment stop surprises before they start.
Safety isn’t a fixed point on a chart—it’s part of our daily rhythm. Line workers hold authority to pause processes if readings drift, with standing rules prioritizing integrity over throughput. Internal training invests hours every month keeping skills sharp and eyes alert. Cross-team discussions break silos and keep innovation linked with on-the-ground practicality.
We recognize industry-wide concern about trace elements or cumulative exposure. Our plant continuously reevaluates handling protocols for sensitive chemical families, ramping up air monitoring, waste stream sampling, and engineering controls after each external benchmark or report. Every improvement threads into production, not just compliance paperwork.
Not every season brings smooth sailing. We have faced upstream raw material delays, regulatory shifts, and even a machinery breakdown or two just as timelines tightened. Every bottleneck taught us to buffer supply, triple-check maintenance logs, and train staff to be fluent with alternative batch protocols. When regulations around certain solvents changed in key export regions, we worked from both ends: qualifying greener substitutes while lobbying for clear labeling rules in international consortia.
Intense competition in this segment pushed us to share test results directly with our clients, speeding up the trust cycle and improving the odds that product works the first time, not after rounds of troubleshooting. We carried lessons from feedback—swift communication, technical hotlines staffed by real chemists, continuous transparency about test results, transport times, and chain-of-custody documentation.
We learned that, above all, the true value of a chemical producer lies in willingness to adapt for the client's ultimate goal. Rather than defaulting to “industry best practices,” we look instead at which users encounter slowdowns, which requests recur, and where innovation breaks down. Out of every misstep—be it a clumping during bulk transfer or minor odor variance—we built new protocols and made our production less about compliance, more about practical, day-in-day-out usability for serious working labs.
The landscape for advanced intermediates just keeps accelerating. Tactical partnerships, smarter digital traceability and easier two-way feedback now drive manufacturing forward. We invite every scientist and process engineer who works with 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine to keep sharing their wishes and worries. Each dialogue sparks new insights, bringing our operation closer to the challenge of truly reliable, practical chemical supply.
Years spent on this line taught us that trusted materials rest not on logos and promises, but on unbroken links between technical rigor, open communication, and relentless attention to detail. Building from molecular building blocks to fully integrated, customer-driven solution streams defines our daily mission—one that keeps moving forward so your next result doesn’t rely on chance, but on proven, repeatable effort from the source.
We commit to being both flexible and picky, agile but stubborn about quality. Every lot of 2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine leaving our line carries the dedication and expertise our team built up over the years. Nothing less matches the needs of those pushing science forward.