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HS Code |
615312 |
| Iupac Name | 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine |
| Cas Number | 134055-06-6 |
| Molecular Formula | C17H23N3O2 |
| Molecular Weight | 301.39 |
| Appearance | White to off-white solid |
| Melting Point | 140-144°C |
| Solubility | Soluble in most organic solvents (e.g., dichloromethane, THF, acetonitrile) |
| Chirality | Chiral (contains (4R) configuration at both oxazoline rings) |
| Boiling Point | Decomposes before boiling |
| Smiles | CC(C)[C@@H]1COC=N1c2cccc(n2)N3=C(C(C)C)COC3 |
| Synonyms | Pybox ligand, (4R)-iPr-Pybox |
| Optical Rotation | [α]D20 +144° (c=1, CHCl3) |
| Functional Groups | Oxazoline, pyridine, isopropyl |
| Usage | Ligand for asymmetric catalysis |
As an accredited 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass bottle with a secure screw cap and clear labeling for safe laboratory use. |
| Container Loading (20′ FCL) | Container loading (20′ FCL): Chemical securely packed in drums, loaded and stabilized; total net weight: 10–15 MT per container. |
| Shipping | The chemical **2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine** is shipped in a tightly sealed container, protected from moisture and light. It is transported according to standard chemical safety regulations, with appropriate labeling and documentation, ensuring secure handling to prevent leaks or contamination during transit. Temperature control may be maintained if specified. |
| Storage | Store 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, in a cool, dry, and well-ventilated area. Protect from moisture, air, and light. Recommended storage temperature is 2–8 °C (refrigerator). Avoid exposure to strong oxidizing agents and acids. Follow standard laboratory safety protocols when handling this compound. |
| Shelf Life | 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine is stable for at least two years when stored cool, dry, and protected from light. |
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Purity 99%: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with a purity of 99% is used in asymmetric catalysis research, where high enantioselectivity is achieved for chiral ligand applications. Molecular weight 285.38 g/mol: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with a molecular weight of 285.38 g/mol is used in coordination chemistry, where precise stoichiometric control improves complex formation efficiency. Melting point 121–124°C: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with a melting point of 121–124°C is used in organometallic synthesis, where stable handling during high-temperature reactions is required. Stability temperature up to 180°C: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with stability up to 180°C is used in catalyst preparation, where thermal resistance ensures ligand integrity during synthesis. Optical rotation [α]D +56° (c=1, MeOH): 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with optical rotation [α]D +56° (c=1, MeOH) is used in chiral transition metal complex development, where chirality transfer leads to improved stereoselective outcomes. Solubility in acetonitrile >50 mg/mL: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with solubility in acetonitrile >50 mg/mL is used in homogeneous catalysis systems, where rapid dissolution accelerates reaction kinetics. HPLC assay ≥98%: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine with HPLC assay ≥98% is used in pharmaceutical intermediate synthesis, where minimized impurities enhance product reproducibility. Storage at 2–8°C: 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine requiring storage at 2–8°C is used in ligand libraries, where controlled storage conditions maintain long-term chemical stability. |
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Moving production chemistry forward means more than offering molecules with a CAS number and a pure label. The backbone of successful synthesis often lies hidden, shaped by ligands that direct and boost the activity of transition metals. 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine, or simply Pybox-iPr, fits this role with a distinct practical value in asymmetric catalysis. Our team does not approach this as a remote concoction, but as a tuned result of years in development, manufacturing, and partnering with researchers seeking high enantioselectivity for challenging transformations.
Chemists look for more than a molecule written on a label. Each batch of Pybox-iPr carries lessons learned from real process feedback. Working with universities and pharmaceutical groups, we found that 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine plays a core part in enantioselective catalysis, specifically in forming C–C and C–N bonds under transition metal catalysis. Its chiral induction lifts stereocontrol in a variety of reactions, and the (4R)-(+)-isopropyl substitution demonstrates superior selectivity where other, more generic pyridine-bis(oxazolines) may fall short.
The oxazoline rings attached to the pyridine scaffold bring both rigidity and tunability. Across repeated batch productions, we’ve observed that the isopropyl group on the oxazoline contributes a sweet spot in both electronic and steric demand. This shows up clearly in asymmetric additions, such as cyclopropanations and allylic substitutions. Our in-process analytics and coordination studies reveal that Pybox-iPr complexes comfortably with metals like copper, iron, and ruthenium, forming robust catalysts that handle scale-up better than their analogs with bulkier or less defined substituents.
Manufacturing experience has a way of cutting through the noise. Catalogs fill with ligands, but not all survive the step from trial flasks to reactors with real throughput. Many researchers reach us with bottlenecks: Standard bis(oxazolines) might deliver selectivity in academic tests but fail in hands-on production due to solubility issues or unpredictable coordination. Pybox-iPr, by contrast, shows clean solubility in common organic systems and exhibits stability across extended runtime. Tracking down reaction progress—especially on larger scale—demonstrated that reactions with our material require less purification, which cuts down on labor and shrink.
Another difference emerges in handling. In practice, some alternative ligands degrade upon storage or exposure to light, leading to inconsistent catalytic results. We run regular shelf-life studies and set aside enough reference material to benchmark each lot. Pybox-iPr maintains its integrity over months under ambient conditions, and our QC team consistently measures batch-to-batch reproducibility using both HPLC and NMR methods. The ligand’s physical form—consistently free-flowing and crystalline, not tacky—remains a repeated point of positive feedback from bench chemists.
Production chemistry meets the ground truth of practical demands. Even small changes in catalyst purity can tilt a whole synthesis away from the desired product. Over the course of hundreds of batches at scale, we’ve standardized our Pybox-iPr at high chemical and enantiomeric purity. Each lot ships with thorough analytical support including chiral HPLC traces and, for larger-scale partners, full impurity profiling. These steps arise not from regulatory concerns alone, but from real production headaches: Early on, we saw that trace impurities—not always visible on basic TLC—could bleed into trouble downstream, especially in pharmaceutical or agrochemical applications.
Typical physical form stays solid and manageable with a melting point consistent between lots. Our teams prioritize ease of weighing and quick dissolution: users tell us this small production detail makes a big difference during campaign work, where every minute counts and solvent loads must be calculated with accuracy. The absence of clipboard-style anti-caking agents or unnecessary formulation reduces the risk of trace contaminants lurking where they can’t be easily detected by routine QC.
For glassware teams and scale-up plants, we receive requests for documentation on trace metals and residual solvents. All Pybox-iPr shipments undergo metal content analysis—the importance of this step became clear from one customer’s scale-up, where an off-spec ligand batch from another vendor meant failed GMP release of a high-value intermediate. Since then, we’ve built metal and residual solvent screening into our process: after final crystallization, every lot is tested in-house before release. These investments stem from feedback, not marketing slogans.
Turning theory into working chemistry requires trust built from repeated, verifiable use. Since introducing our 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine process, we’ve helped companies shift from small-batch trials into kilogram and multi-kilogram productions. In one instance involving the development of an API intermediate, a major pharmaceutical partner saw step yield and enantiopurity increase consistently when switching from an earlier ligand mix—our compound supported repeated, stable cyclopropanations with improved throughput. Documented reductions in side products meant a lighter downstream purification load, and the shortened timeline lent the project real savings in both labor and spend.
Our own technical support teams have run trials in parallel with end-users and fielded direct questions arising during process development. One recent collaboration focused on copper-catalyzed asymmetric borylation: in a side-by-side comparison with alternative ligands, Pybox-iPr delivered higher enantiomeric ratios and supported fast catalyst turnover even in the presence of air-sensitive substrates. We routinely receive sample requests from chemists struggling with reproducibility or looking to reduce catalyst costs without stepping down on performance.
Consistency in use isn’t a vague claim—it’s the result of live tracking of reactions, feedback from analytical teams, and root-cause investigations when a campaign faces bumps. Each time a customer identifies a bottleneck—like incomplete conversion or slow product isolation—our technical team reviews lot histories and digs into possible micro-impurities, solubility changes, or subtle storage artifacts. Tens of scale-ups and multistep syntheses later, we see the practical value of Pybox-iPr clearest in the successful delivery of high-added-value products to clinical and commercial pipelines.
No one likes to waste time reordering ligands, troubleshooting reactions, or discarding failed batches due to decomposition. Pybox-iPr’s stability stands out in climates ranging from humid coastal labs to drier inland facilities. Our packaging process, built on lessons from failed early shipments, now uses high-barrier materials that prevent moisture ingress and light contamination. Each bottle seals tight, but end users in our regular survey remind us to provide guidance for transfer and storage under argon or nitrogen for the most sensitive applications. On the rare occasion when a customer encounters clumping or color change, we walk through storage conditions and replace the affected lot if necessary. A consistent storage guideline now accompanies all shipments, developed not as boilerplate but from analysis of real-world storage failures and their root causes in the field.
Safety, too, creates fewer headaches when both manufacturer and end-user understand and communicate regularly. Working closely with production supervisors and bench chemists, we track all changes in raw material supply and flag possible reactive intermediates in our internal syntheses. Our process never cuts corners by using lower-quality starting materials or off-spec solvents. Regular hazard checks, coupled with detailed lot records, back up the long-term safety of the ligand in regular use. Our technical group maintains protocols for safe weighing, solvent selection, and appropriate PPE, all of which stem from our daily experience and ongoing dialogue with industry partners.
Scaling a reaction from milligrams to multi-kilogram quantities isn’t as simple as multiplying the recipe. Over the years, we’ve worked with partners stuck in the “valley of death” between R&D and commercial production. One issue repeated across projects is that the ligand—often supplied at a small scale by a specialty vendor—turns out variable, poorly characterized, or unavailable in timeline-matching lots. With Pybox-iPr, commitment to stability and reproducibility has meant adjusting our synthesis strategy, working with raw materials suppliers to ensure consistent quality, and keeping clear communication lines with procurement and technical teams on customer sites.
Field reports keep proving how this work pays off. One plant chemist described a ligand-based catalysis route that worked fine in a glovebox, but failed at plant scale because the commercial ligand failed to match the research purity or physical form. Ever since, we have run close parallel checks with pilot-scale end users—realign every production variable, from particle size to drying temperature, to ensure the Pybox-iPr reaching your plant matches the chemist’s original bench sample. We never rely on a single analytical approach: using orthogonal detection (NMR, HPLC, GC-MS), we follow each batch’s performance in downstream reactions and document the cycle to establish reproducibility.
Production chemistry thrives on feedback loops. The best process improvements come from open dialogue—not from forms or scripts, but from chemists working late, troubleshooting bottlenecks. Over the past decade, our product team developed a program to log, investigate, and solve field issues. For Pybox-iPr, this often means responding to requests for process tweaks, guidance on optimal addition sequences, or deeper insight into handling sensitive transition metals.
One customer faced with a stalled asymmetric synthesis uncovered a subtle impurity carried over from a competing supplier’s ligand. On switching to our material, they saw the troublesome side reaction disappear—our lot-specific trace impurity screens, included with every commercial shipment, allowed them to quickly move forward. That experience spurred improvements in our own documentation and communication strategy, adding a custom support channel for research leads and scale-up engineers. No generic FAQ or chatbot: every question receives a hands-on answer from staff with direct lab or plant experience.
Beyond shortcuts and bottlenecks, our technical group takes part in regular knowledge-sharing workshops, both virtual and on-site. We do not treat application notes as marketing—each document summarizes field results with reaction protocols developed, tested, and refined in living labs. Chemists and engineers benefit from these applied insights, which reflect repeated hands-on work, not literature summaries or catalog curation. Our mission: help customers bring their best chemistry to life through reliable, fully characterized materials that never leave them guessing on performance or supply.
Modern specialty chemicals face higher scrutiny—not just for quality, but for environmental and ethical production. Over the years, we’ve revamped our process for Pybox-iPr to minimize waste, recover solvents, and avoid hazardous intermediates where feasible. Energy-efficient reaction conditions have become standard. This reduces not only our own environmental footprint, but the on-site hazard load for downstream users.
Transparency also means sharing real information, not green-washed claims or vague “commitments.” Detailed batch records, traceability reports, and regular environmental audits—shared on request—keep our process open to regulatory and customer review. Customer audits are welcomed, and the feedback feeds directly into process improvements. This ongoing accountability builds trust with partners across pharma, agrochemical, and research sectors, all of whom recognize that shortcuts in upstream production can lead to downstream risk.
Past experience shapes robust products—each production run, each field complaint, each resolved trouble ticket. We keep expanding our practical knowledge base as customers find new applications for 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine, whether in next-generation intermediates or in fields beyond pharma and fine chemicals. Our goal is not only to deliver material, but to back the user's journey with real answers, deep product knowledge, and the willingness to adapt our manufacturing as needs shift.
Part of thriving as a chemical manufacturer is humility—accepting feedback, admitting error, and returning better with each lot. The best process improvements come straight from the shop floor or the project site: a change in drying schedule, a tweak in purification, an advisory on optimal storage, or a heads-up about a shifting market demand. Each partner brings new insight, and our own road towards better, more effective ligands grows richer with shared experience.
The evolution of 2,6-bis((4R)-(+)-isopropyl-2-oxazolin-2-yl)pyridine demonstrates that even a “small” component in a catalytic system can drive major gains in process output, scale, and product quality. As synthetic challenges mount in fields ranging from pharmaceutical actives to new polymer architectures, the need for reliable, well-characterized chiral ligands only increases. Our work remains grounded in direct engagement—listening to the bench, testing in real systems, and always shipping with documented, proven performance behind every bottle. Chemists have enough unknowns in their daily work; with Pybox-iPr, our promise remains clear: consistency you can count on, and a team committed to the ongoing, often unpredictable reality of production chemistry.