|
HS Code |
496414 |
| Chemical Name | R-1,1'-Bi-2-Naphthol |
| Synonym | (R)-BINOL |
| Cas Number | 18531-94-7 |
| Molecular Formula | C20H14O2 |
| Molar Mass | 286.32 g/mol |
| Appearance | white to off-white crystalline powder |
| Optical Purity | typically >99% ee |
| Melting Point | 191-193°C |
| Solubility | sparingly soluble in water; soluble in organic solvents |
| Specific Rotation | [α]D20 +35° to +38° (c=1, ethanol) |
| Storage Conditions | store at 2-8°C, tightly closed |
| Chiral Purity | high enantiomeric purity |
| Application | chiral ligand in asymmetric synthesis |
As an accredited R-1,1'-Bi-2-Naphthol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for R-1,1'-Bi-2-Naphthol (25g) is a sealed amber glass bottle with a secure polypropylene screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 8 metric tons of R-1,1'-Bi-2-Naphthol packed in 25kg fiber drums or as customer required. |
| Shipping | **R-1,1'-Bi-2-Naphthol** is shipped in tightly sealed containers, protected from light and moisture. Standard transport occurs at ambient temperature unless otherwise specified, with appropriate hazard labeling. Packaging complies with chemical safety and regulatory requirements to prevent spills or contamination during transit. Verify specific shipping class and documentation before dispatch. |
| Storage | R-1,1'-Bi-2-Naphthol should be stored in a cool, dry, and well-ventilated area, protected from direct sunlight and incompatible substances such as strong oxidizers. The container should be tightly closed to prevent moisture absorption and contamination. Label containers clearly and store away from sources of heat and ignition. Use personal protective equipment when handling to avoid skin or eye contact. |
| Shelf Life | R-1,1'-Bi-2-Naphthol has a typical shelf life of 2-3 years when stored in a cool, dry, and dark place. |
Competitive R-1,1'-Bi-2-Naphthol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
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Every batch of R-1,1'-Bi-2-Naphthol that leaves our facility represents more than its chemical identity and purity figures: it captures years of work spent refining reproducibility and tackling the practical demands we’ve encountered across sectors, especially in chiral catalyst production and asymmetric synthesis. We focus obsessively on controlling quality and minimizing batch-to-batch variability, as these points define how easily downstream users can rely on their process outputs. In comparison with other compounds in the binaphthol family, R-1,1'-Bi-2-Naphthol, sometimes called BINOL, holds a distinct position for its chiral induction properties and the level of reproducibility we have come to expect and demand internally, both for smaller laboratory needs and industrial-scale campaigns.
The primary difference starts at the production floor. Years ago, too many commercial suppliers—especially trading intermediaries—treated R-1,1'-Bi-2-Naphthol as a mere commodity, pushing for volume. Our approach turned to the subtleties of purification and crystalline consistency, since even minor impurities can spiral into yield or selectivity issues in real-world fine chemical reactions. We run comparative trials, not just on the analytical data, but in typical reaction setups observed at actual client sites. It’s the unexpected reality: a specification sheet rarely covers each parameter that affects stereoselectivity in a multi-step asymmetric process, and our partnership with academic and industrial chemists has exposed these gaps time and again.
Producing R-1,1'-Bi-2-Naphthol involves starting from naphthol derivatives under carefully controlled oxidative coupling conditions. We’ve modified the control of temperature profiles and solvent selection over successive campaigns, learning from some early misfires that heavier reliance on automation produces uneven outcomes for delicate chiral molecules. Our production chemists run regular hands-on audits; they know from experience that even a minor drift in residence time or trace metal contamination can impact the optical purity. Unlike better-known base chemicals, you cannot “fix” out-of-spec BINOL with secondary purification without introducing the risk of crystalline form shifts or unwanted solvates, both of which affect downstream use for phosphine ligand synthesis or other catalytic applications.
We don’t publish numbers just to check a regulatory box. Optical rotation, HPLC chiral purity, and residual solvent content are data points that inform our process corrections week by week. One reason we consistently have returning customers is that their teams have tried equivalent materials from other vendors, only to find variabilities that don’t show up until scale-up: suddenly, a batch of a once-familiar chiral catalyst performs unpredictably, requiring diagnostic time and often causing missed deadlines. Our entire workflow, from raw material sourcing through final filtration and packaging, pushes for consistency, because our own pilot lines demand reliability before customers ever see the product.
R-1,1'-Bi-2-Naphthol has carved a unique space in asymmetric catalysis. Synthetic organic chemists reach for it when their targets demand enantioselectivity that simpler ligands fail to achieve. In our interactions with pharmaceutical process teams, the appeal comes not only from its established or literature-known transformations, but from its “safer bet” status—BINOL-based ligands unlock both higher yields and better enantiomeric excess, especially under sensitive reaction conditions common in multi-step syntheses. Because we ship in a range of quantities, from small R&D packages to large multi-kilogram lots, we get direct feedback from users troubleshooting reactions at both ends of the scale: bench to kilo plant.
When supplying material for binaphthol-derived phosphoric acids or other chiral Lewis acids, we pay attention not just to the chemical structure but also to physical attributes like particle size. Poorly controlled crystallinity or inconsistent micronization can slow dissolving rates, frustrate scale-up processes, and even cause plugging in tube reactors, which feeds directly into production downtime. Our years of feedback loops with users keep us focused on parameters beyond the certificate of analysis; this level of practical input comes only from direct involvement in both manufacturing and support of real-world chemical production.
Customers often ask why the R-enantiomer of 1,1'-Bi-2-Naphthol matters, given the existence of both S and R forms, as well as functionalized derivatives. In the manufacturing context, the difference runs much deeper than a rotated molecular model. Catalyst and ligand demand in asymmetric synthesis hinges on “matching” the chirality of the auxiliary with the required sense of induction in target reactions. The R-form dominates in specific ligand systems, and process engineers in pharmaceutical and agrochemical firms know that a change in enantiomer leads to flips in product selectivity or incorrect assignment of absolute configuration, which no one wants to discover post-launch.
Some customers look for cost savings by considering mixed-enantiomer or racemic binaphthols. We have handled many consultation sessions to troubleshoot those choices, which often end up costing more money and production capacity than initially projected. You can’t recover from enantioimpurity in a ligand once it enters a multistep synthesis route designed for a single enantiomer: yields, regulatory filings, and safety assurances all get tangled in extra QA and analytical review. This is why we adhere tightly to optical purity standards and bear the brunt of the cost for high-end resolution and purification methods.
Compared to more functionalized BINOL derivatives—those bearing halogens, sulfonic acids, or additional aryl groups—R-1,1'-Bi-2-Naphthol provides a well-established platform for further modification. Many users rely on the base compound as a springboard for their own derivatization, finding that starting from a high-optical-purity, uncontaminated batch cuts down on overall project timeline. Functionalized derivatives sometimes require extra regulatory review or custom analytical validation; a stable, reliable R-BINOL simplifies both compliance and downstream chemistry.
Internally, our focus doesn’t just rest on achieving the “typical” purity figures. Most traders recite the 99%+ chemical purity or optical rotation, but our in-house results commonly exceed these, reflecting lessons learned after years of handling both R&D and large commercial volumes. Achieving low water and minimal residual solvent content avoids unexpected hydrolysis or side reactions, notorious for causing expensive re-runs at client sites. We subject each lot to multiple chiral HPLC analyses—more than just the certificate minimum—to catch minor enantiomeric drifts invisible by NMR or IR alone.
We’ve faced situations where competing materials, despite matching numbers on paper, revealed trace coloration or off-odors—signs of minor decompositions or contamination from insufficient purification or poor storage. These experience-driven checks set us apart: we routinely reject in-house lots that meet only the letter of specifications but fail our longstanding “real-application” trials. Not every user will spot small deviations in color or melting point, but these markers tell our technical teams which material will stand up to long-term storage or exposure to typical laboratory atmospheres.
We avoid routine fraction blending, a practice some industry players employ to maximize yield from less-than-perfect production runs. Though blending raises nominal output figures, it introduces risk of hidden variability in end-use performance. Our teams prefer to sacrifice some yield for uncompromised batch identity and traceability, principles that have earned us trust with customers whose research or production budgets cannot afford guesswork.
Many BINOL producers outside of direct manufacturing underestimate what happens when processes leave the bench. During a transition from gram-scale laboratory experiments to full-scale production, unexpected issues like solubility changes, filter plugging, or crystallization rate shifts can derail otherwise reliable transformations. We attend these scale-up runs, monitor for off-gassing or mixing issues, and keep records of which lots react best for ligand synthesis, resolution protocols, or subsequent derivatizations.
Our years of feedback with process engineers have shown the importance of maintaining consistent particle morphology, not just bulk purity. One batch with unexpectedly large needle-like crystals can cause stubborn filtration slowdowns, while another with excessive fines triggers dust hazards for plant crews. Our standardization efforts go well beyond the bulk assay figures, focusing instead on how the material “runs” in actual synthesis campaigns, especially where continuous or semi-batch processes are employed.
From running side-by-side comparisons of “our material vs. other manufacturers,” we found real operational savings: fewer re-solubilizations, lower clogging rates, and more predictable downstream processing when sourcing directly from a manufacturer. These results come from hundreds of pilot trials and close collaboration with on-site chemists, not just sales data or spec-sheet matching. Rather than maximizing short-term yield per batch, we invest in process improvements, testing, and knowledge-sharing that pays off through fewer headaches for everyone using the product.
As basic upstream feedstocks and processing aids change, our technical teams revalidate every substantive material characteristic. For R-1,1'-Bi-2-Naphthol, the increasing demand for high optical purity in single-enantiomer drugs means we can’t ignore even minor shifts in precursor quality or process conditions. Over the last decade, we’ve swapped in more tightly controlled oxidation agents, shifted away from problematic metals, and modified our crystallization regimens. These changes, born out of recurring customer challenges, have moved us beyond the once accepted “good enough” to a process that tolerates real-world supply fluctuations without sacrificing results.
Some issues still linger in the wider market. We regularly see competitors skipping key cleanup steps or accepting visually off-spec material during periods of supply-tightness. Our view, shaped by past disasters (including delayed pharmaceutical registrations and big-ticket plant shutdowns), holds that false economy at the manufacturing stage only shifts the burden downstream—to customers, regulators, and sometimes end-users. Experience shows that the extra time and cost spent correcting small lot variances ahead of shipment always pays back many times over.
Even as new synthesis protocols emerge, R-1,1'-Bi-2-Naphthol continues to serve as both a reliable chiral backbone and a benchmark for production discipline. The company’s technical leaders often serve in a consultative role for researchers exploring novel catalytic systems or ligand modifications, offering practical guidance on material compatibility, handling protocols, and strategies for minimizing waste in recovery or recycling. Our deep familiarity with R-1,1'-Bi-2-Naphthol’s strengths and possible pitfalls leaves us uniquely positioned to help customers adapt their workflows as research and applications evolve.
It’s easy to underestimate how much practical trouble and opportunity hides between lines on a specification sheet. Producing R-1,1'-Bi-2-Naphthol as a direct manufacturer unlocks visibility into problems and their real fixes. We’ve had to remedy run-to-run variation by investing in better spectroscopic monitoring and data analysis tools, cutting turnaround time from feedback to process change. Nearly every process improvement in our factory originated from a customer’s unexpected result: complaints about reaction rates, color formation, or filtration issues lead us to test hypotheses, run pilot trials, and revisit raw material supply chains.
By serving as an active collaboration partner for customers—especially those scaling up asymmetric syntheses or developing new iterations on BINOL chemistry—we close gaps that paper specifications leave open. Case in point: during a recent push by several global API manufacturers to drive down catalyst-related costs, our technical input on minimizing ligand waste points, optimizing recoveries, and enhancing binaphthol recovery circuits led directly to asset utilization improvements and reduced environmental impact, which no catalog data would have revealed.
In practice, material that delivers in the lab but disappoints at scale can derail months of project planning. As direct producers, we’re positioned to monitor every variable, so technical teams don’t face surprises down the line. Over the years, our willingness to recall suboptimal lots, absorb lost revenue, and continually document all learning points has laid the foundation for mutual trust with our customers. They return for the promise that their next delivery will reflect not just the same purity and chiral quality, but every lesson we’ve recently collected throughout our production lines. That’s a benefit that rarely comes from a trader or a distributor relying on external supply and unaware of all the invisible links in the chain.
As regulatory regimes tighten and pharmaceutical standards evolve, R-1,1'-Bi-2-Naphthol continues to command close attention at all points in its lifecycle. Our direct oversight, from feedstock selection through to final shipment, creates an connection with the material that goes beyond audit trails or certificates. In a world where “commodity” suppliers race each other to the lowest price, our customers have found greater value in reliability, transparency, and hands-on technical support spanning years and countless chemical campaigns. BINOL derivatives remain the heartbeat of chiral technologies across diverse industries, but sustaining their practical use depends on this deeper, more direct engagement with what truly defines quality.
For chemists pushing new frontiers in catalysis, researchers scaling their best ideas to market, and manufacturers required to meet the tightest enantioselective standards, R-1,1'-Bi-2-Naphthol isn’t just another lot number or catalog entry. Its story runs through every lesson learned on our production floor—a timeline of adjustments that has made each new order more dependable and every process outcome more predictable. This experience, hard-won, continues to shape not just how we produce and deliver, but how we view our partnership with the people and industries that depend on R-1,1'-Bi-2-Naphthol every week.