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(-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate

    • Product Name (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate
    • Alias (R,R)-Me-BPE-Rh(cod)BF4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    635733

    Product Name (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate
    Abbreviation Rh(cod)(MeO-Biphep)BF4
    Chemical Formula C32H44BF4P2Rh
    Molecular Weight 689.22 g/mol
    Appearance yellow to orange solid
    Cas Number 282863-96-3
    Solubility soluble in dichloromethane, chloroform, and tetrahydrofuran
    Storage Conditions store under inert atmosphere, at 2-8°C
    Purity typically >98% (as supplied)
    Application used as a catalyst for asymmetric hydrogenation
    Chiral Ligand utilizes (2R,5R)-dimethylphospholane ligands
    Oxidation State Rhodium +1
    Counterion tetrafluoroborate (BF4-)
    Sensitivity air and moisture sensitive
    Synonym (-)-Rh-MeO-Biphep-(COD)-BF4

    As an accredited (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 1-gram packaging consists of a sealed amber glass vial with a screw cap, labeled with product details and safety warnings.
    Shipping This chemical is shipped in a tightly sealed container under inert atmosphere, such as nitrogen or argon, to prevent degradation. It is packed with appropriate cushioning materials, temperature control if required, and labeled according to international regulations for hazardous materials. Shipping complies with DOT, IATA, and IMDG guidelines.
    Storage Store **(-)-1,2-Bis[(2R,5R)-Dimethylphospholano]benzene(cyclooctadiene)rhodium(I) tetrafluoroborate** under an inert atmosphere (e.g., nitrogen or argon) in a tightly sealed container. Keep it in a cool, dry place, protected from light and moisture. Avoid exposure to air and oxidizing agents. Refrigeration (2–8°C) is recommended for long-term stability. Handle inside a glovebox or using Schlenk techniques if possible.
    Application of (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate

    Applications of (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate in Industrial Manufacturing

    We supply (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate directly from our proprietary synthesis facilities to support industrial users who demand high performance in asymmetric hydrogenation and chiral synthesis. The following application scenarios reflect established downstream use cases embraced by the world’s leading innovators in pharmaceuticals, fine chemicals, agrochemicals, and specialty materials manufacturing. Each application is backed by relevant sector standards, realistic process parameters, and actual end-use integration.

    1. Asymmetric Hydrogenation in Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers apply this rhodium-based chiral catalyst in the enantioselective hydrogenation of prochiral olefins, ketones, and enamides during API intermediate production. The superior enantioselectivity directly impacts the stereochemical purity of the resulting molecules, which is crucial for drug approval and therapeutic consistency. The catalyst’s high turnover frequency allows efficient incorporation in continuous or batch processes for both small- and large-volume intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapters <467>, <232>, <233> for elemental impurities
    • FDA 21 CFR Part 211—cGMP for finished pharmaceuticals
    • EMA Guideline on the Specification Limits for Residues of Metal Catalysts

    Typical usage ratio

    • 0.05–0.3 mol% relative to substrate; adjusted for substrate complexity and desired enantiopurity

    Downstream process integration

    • Introduction during the hydrogenation stage after substrate preparation and solvent charge
    • Catalyst removal and recovery by filtration and washing before downstream purification

    Final product types

    • Enantiomerically pure pharmaceutical intermediates
    • Certified chiral APIs for cardiovascular, CNS, and anti-infective drug classes

    2. Enantioselective Hydrogenation in Agrochemical Synthesis

    This catalyst finds routine deployment in the synthesis of chiral agrochemical actives, enabling efficient production of enantiopure pesticides, herbicides, and fungicides. The precise control of chirality is necessary to ensure biological activity, reduce off-target effects, and conform to regulatory purity requirements. Agrochemical operations often emphasize catalyst recovery and recycling to optimize cost and meet environmental regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 0.08–0.25 mol% relative to prochiral substrate; exact ratio set by substrate load and targeted enantiopurity

    Downstream process integration

    • Catalyst addition occurs during enantioselective hydrogenation following substrate solubilization
    • Catalyst separation completed by phase filtration post-reaction; residual levels monitored in QC release

    Final product types

    • Enantioselective intermediates for triazole- and pyrrole-based crop protection compounds
    • Chiral insecticides and plant growth regulators

    3. Synthesis of Chiral Amino Acid Derivatives in Fine Chemical Production

    Leading fine chemical plants use this catalyst to produce optically active amino acid derivatives via hydrogenation of dehydroamino acid esters and enamides. The approach enables scalable access to specialty chiral building blocks required for further derivatization in peptide synthesis, fragrance manufacture, or as catalysts themselves. In these operations, process engineering frequently tunes hydrogen delivery and substrate concentration to optimize conversion and catalyst longevity.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems
    • Responsible Care® Commitment by the International Council of Chemical Associations
    • Internal QC per product specification sheets
    • REACH pre-registration for specialty chemical substances

    Typical usage ratio

    • 0.1–0.5 mol% based on substrate, with adaptation for process scale and batch versus continuous operation

    Downstream process integration

    • Hydrogenation reactor charge post-substrate and solvent addition
    • Catalyst removed by microfiltration before downstream purification or crystallization

    Final product types

    • Chiral amino acid esters
    • Enantiomerically enriched peptide intermediates
    • Flavor and fragrance chiral synthons

    4. Enantioselective Alcohol Formation in Specialty Materials Manufacturing

    The catalyst is relied on for industrial-scale production of chiral alcohols required in high-performance polymers and advanced monomers for functional materials. Manufacturers value the catalyst for its selective hydrogenation of prochiral ketones. The resulting chiral alcohols impart key physical properties to specialty resins and optoelectronic materials, enabling differentiation in end-use product performance and consistency in technical applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive 2011/65/EU (for electronic materials)
    • QMS protocols for polymer intermediates (internal controls)
    • REACH declarations and reporting for specialty chemicals

    Typical usage ratio

    • 0.07–0.3 mol% based on carbonyl starting material; finetuned for product isomeric purity demand

    Downstream process integration

    • Catalyst enters hydrogenation stage after feedstock preparation
    • Spent catalyst removed by solid-liquid separation before product work-up and isolation

    Final product types

    • Chiral diols and polyols for engineering resins
    • Building blocks for optically active monomers
    • Specialty plasticizers and performance additives

    5. Catalytic Reduction of Prochiral Enamines for Custom Ligand Production

    In advanced ligand manufacturing, this rhodium catalyst functions as the key asymmetric hydrogenation agent for prochiral enamines, supporting the scalable synthesis of custom ligands required in next-step pharmaceutical or polymerization catalyst systems. Manufacturers prioritize reproducibility and precise enantiopurity control when setting parameters, as these ligands strongly influence resultant catalyst functionality and downstream product properties.

    Industry compliance standards

    • SOCMA ChemStewards® or equivalent Responsible Manufacturing frameworks
    • ISO 9001:2015 Quality Management System (for catalyst components)
    • REACH compliance for specialty ligands
    • Custom QC protocols based on ligand client specs

    Typical usage ratio

    • 0.1–0.3 mol% relative to enamine substrate; established by required ligand enantiopurity and final application specs

    Downstream process integration

    • Catalyst charged to reduction stage following substrate blending in reactor
    • Catalyst removed by filtration or decantation after selective hydrogenation and before chromatographic purification

    Final product types

    • Chiral phosphine ligands for pharmaceutical catalysis
    • Optically pure ligands for custom polymerization initiators
    Free Quote

    Competitive (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate: Precision Catalyst from the Source

    Direct Experience in Precision Catalysis

    At our facility, manufacturing asymmetric catalysts isn’t a generic process. Each batch of (-)-1,2-Bis[(2R,5R)-Dimethylphospholano]Benzene(Cyclooctadiene)Rhodium(I) Tetrafluoroborate—often called (R,R)-Me-DuPhos Rh(COD)BF4—draws on decades of hands-on synthesis and thousands of hours spent scaling phosphine ligand-based complexes. Chemists in the lab don’t merely look for product yield; focus hones in on purity, chiral induction, and most importantly, reproducibility.

    Through the years, we have refined the synthesis, tuning the air-free processes required to maintain the integrity of the phospholano ligands. With this work, we ensure that every vial of this rhodium complex delivers the consistent enantioselectivity that researchers and process developers have come to expect in hydrogenation applications.

    Distinct Nature of (R,R)-Me-DuPhos Rh(COD)BF4

    Catalysis poses unique challenges in asymmetric synthesis, especially where regulatory agencies scrutinize the stereochemistry in every lot of new drug candidates. One-size-fits-all catalysts simply can’t meet the selectivity and turnover demands for today’s pharmaceutical and fine chemical industries.

    The ligand environment of (R,R)-Me-DuPhos Rh(COD)BF4 delivers a unique chiral envelope; we know from both our in-house studies and industry collaborations that the (R,R)-dimethylphospholano groups provide the right bite angle and electron density to maximize both reactivity and selectivity, especially in enantioselective hydrogenations of functionalized olefins. The robust nature of this complex stems from the cyclooctadiene ligation, which supports the rhodium center yet enables substrate exchange without excessive ligand loss. That stability only comes from careful handling at every step: inert conditions, anhydrous solvents, controlled temperature—process factors we monitor tightly.

    Specifications Born of Direct Handling, Not Marketing Sheets

    We don’t copy figures from catalogues. Every lot faces full spectroscopic analysis by NMR and HPLC. The enantiopurity of the ligand and the integrity of the complex both matter. Through years of real use, we’ve observed even minor variations in synthetic steps—a single degree in temperature swing, a slightly different batch of starting phosphine—leads to measurable differences in catalytic efficiency or byproduct formation. That’s the perspective of a manufacturer who actually tracks these variables, not just a repackager moving bottles around.

    Most customers can expect our product to arrive as a yellow, air- and moisture-sensitive powder. Depending on the hydrogenation process, users sometimes dissolve it in dichloromethane, THF, or toluene, then introduce the substrate under an inert atmosphere. We send each batch with full documentation, but more importantly, with chemists ready to answer practical questions from researchers running high-pressure reactions or optimizing for gram-to-kilo scale transfer.

    Why This Catalyst Outperforms Generic Rhodium Complexes

    Simple rhodium COD complexes may serve as workhorse catalysts, but the leap in performance from (R,R)-Me-DuPhos Rh(COD)BF4 is visible in the data and on-process outcomes. Take enantioselective hydrogenation of dehydroamino acid derivatives: generic triphenylphosphine rhodium complexes often give mixed results, high variability lot-to-lot, and struggles with challenging substrates. In contrast, this proprietary phospholane-based catalyst repeatedly delivers >95% ee and turnover frequencies that cut production time. We have seen projects transition from exploratory chemistry to commercial launch by switching to our product, thanks to tighter chiral control and higher throughput.

    Every process chemist working at scale encounters catalyst degradation and recycling issues. Using the (R,R)-Me-DuPhos ligand scaffold, catalyst stability withstands multiple batch additions and allows for practical recycling in certain set-ups. Differences like these come from deeper materials handling experience, not marketing claims.

    Lessons Learned From Manufacturing for Industry

    Working as the producer—sourcing raw phosphorus compounds, purifying ligands, and ligating metals—provides a perspective not shared by those who only resell. Direct access to customer feedback informs improvements in formulation and packaging. Often, we’ve received samples back from pilot plants where minute changes in phospholano ligand purity noticeably affect product quality. That prompted development of an improved ligand purification process, which we validated with both NMR and a pilot hydrogenation test on a pharmaceutical intermediate. This attention to feedback led to a drop in both off-spec batches and downstream processing headaches.

    It’s not uncommon to see “the same” product offered by different vendors, but users quickly realize differences in shelf life, solubility, or catalyst activation time. We field calls from chemists who switched over from a lower-priced vendor, only to find inconsistency under process conditions. That’s a result of shortcutting steps like precise pH control during crystallization, or skipping critical air-exclusion measures. Our process controls extend throughout the value chain: sourcing ligands, verifying chiral purity, all the way to final packaging under argon.

    Supporting Users Beyond the Sale

    Large-scale asymmetric hydrogenations demand not only a reliable product but also direct technical support. We often engage with chemists optimizing reductions of β-keto esters, unsaturated lactams, or complex heterocycles. Many times, the first trial conditions do not yield optimal results. Sharing best practices for in situ substrate activation or common pitfalls in reactor setup comes naturally from years of seeing this catalyst run on different production lines.

    Troubleshooting after delivery forms a daily part of our work. Examples range from guiding a start-up’s new pilot plant on degassing procedures, to collaborating with process engineers adjusting the base or solvent system. With far less downtime and fewer batch failures, users return for advice on scaling up heterogeneous support strategies, or reusing catalyst beds under continuous flow.

    Reducing catalyst use without compromising yield represents a main driver for both cost and sustainability in chemical manufacturing. Because we control the ligand quality from scratch, we can share data on optimal ligand loadings and best rhodium-to-substrate ratios. That data stream runs both ways—feedback from application partners leads to improvements that benefit the next user. Few trading houses can match that ongoing collaboration.

    Meeting New Regulatory and Environmental Demands Head-On

    The push for cleaner processes, lower metal content in actives, and demonstrable green credentials influences every decision we make. Manufacturing (R,R)-Me-DuPhos Rh(COD)BF4 requires not only chemical precision but lifecycle vigilance. Waste minimization starts at the kilogram scale, where efficient ligand use and solvent recovery drive both compliance and cost savings. In the past two years, pharmaceutical partners have required ever lower rhodium residuals in APIs, pushing us to refine both catalyst removal protocols and in-line process monitoring. From direct experience, residual metal content tracks back to catalyst purity, not just to filtration or wash steps downstream. Doing the chemistry right at the primary manufacturing phase pays dividends in easier process qualification.

    Within the lab, our teams run ongoing studies to reduce environmental impact—recovering and recycling mother liquors, implementing nitrogen-blanketed packaging lines, and switching to greener solvents in certain critical steps. For every process increase in scale, environmental reports update to reflect actual, audited data from our operations.

    We recognize customers face tighter waste handling and reporting rules every year. In response, we’ve adjusted pack sizes and container materials to facilitate easy, compliant disposal, and can advise on process adaptations for catalyst reclamation or waste minimization.

    Real Differences from Other Ligand Systems

    Many asymmetric rhodium catalysts employ BINAP or Monophos-type ligands. Through rigorous internal studies and application feedback, we have seen (R,R)-Me-DuPhos ligands outperform these alternatives in several respects. The fused phospholano rings create a steric environment that blocks undesired side attack on substrates, leading to higher selectivity in difficult substrates—such as challenging α,β-unsaturated carboxylates or functionalized alkenes that routinely give mixed products with broader ligands. Reaction time often shortens by up to 30 percent when moving from BINAP to this system, particularly in hydrogenation steps where speed makes or breaks a commercial campaign.

    Competing products may offer comparable optical purities on paper, but inconsistent lot history or shorter shelf life often forces direct users to recalibrate conditions between batches. We push every batch through full trace analysis from ligand synthesis to metalation, monitoring even low-level impurities that can poison catalyst sites in use. This reduces risk of line stoppage and enables chemists downstream to keep process parameters locked.

    Because our site also produces several types of chiral phosphines, we spend time comparing catalyst lines in real head-to-head tests. Each time, the Me-DuPhos system delivers tighter ee control, and holds up under higher turnover conditions—factors measured not by press releases, but by yields reported from the production floor.

    Pushing Forward: Solutions to Persistent Catalysis Challenges

    No catalyst system solves every problem. Even (R,R)-Me-DuPhos Rh(COD)BF4 shows limits with some sterically hindered or very electron-deficient substrates. Our approach is to keep close communication with end users, sharing experimental notes and brainstorming auxiliary ligand modifications or co-catalyst options. Technical staff regularly synthesize analogs in response to partners’ specific needs, and where possible, supply samples for direct testing before committing to scale-up.

    Another challenge involves catalyst recovery and recycling—real-world factors for any process with expensive precious metals. Reclaim protocols developed in-house have lowered rhodium losses by up to 15 percent in several partner sites, primarily through improved ligand removal steps and careful pH control in washes. In some cases, minor changes in solvent polarity or order of addition yield much better catalyst reusability, and we freely share these strategies with trusted customers.

    Packing and transport represent an unglamorous but vital link in the chain. Every year, we address real-life feedback—such as a batch freezing during winter transport, or static discharge issues in dry climates—by tuning packaging and adding monitoring stops for cold chain breaks.

    Future Proofing with Data and Trust

    We believe that chemical manufacturing thrives on direct laboratory experience, validated process data, and open exchange of both problems and wins. That caries through in every shipment of (R,R)-Me-DuPhos Rh(COD)BF4. We keep detailed archives of spectral data and performance logs for every lot, and invite customer audits—face-to-face, not via form letters—to keep our process transparent and continuously improving.

    Scientists on our team have run these catalysts on the bench and in plant environments. They track every kg in, every batch out, and trace minor process tweaks to measurable product benefits. Direct engagement with users keeps job satisfaction high and product development closely aligned with reality, not market hype.

    Supply partnerships now extend over decades, thanks to real attention to detail, careful sourcing, and a refusal to cut corners for expediency. The development of (R,R)-Me-DuPhos Rh(COD)BF4 took patience and persistence, hearing out real-world chemists working in tight regulatory or budgetary constraints, and responding not with “off-the-shelf” promise but with practical, tested product improvements.

    Customer-Driven Adaptation in a Demanding Market

    The pace of change in pharmaceutical and specialty chemical manufacturing won’t slow down. Demand for higher selectivity, greener chemistry, and lower costs drives deeper innovation. Our approach: keep chemists, engineers, and operations teams involved at every point from raw material sourcing to process validation.

    Users expect and deserve honest answers about what works, what doesn't, and why a given batch behaves differently from one month to the next. Being a true manufacturer—directly accountable for synthesis, analysis, and outcome—means we stand behind the performance of (R,R)-Me-DuPhos Rh(COD)BF4 with data, not promises, and with a willingness to help fine-tune processes on demand.

    Decades of accumulated production, troubleshooting, and feedback from the field have shaped a more reliable, reproducible, and effective asymmetric hydrogenation catalyst. We invite the next generation of chemical innovators to bring their toughest projects and questions, and join us in advancing both the chemistry and its real-world impact.