Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Isopropyldiphenylphosphine

    • Product Name Isopropyldiphenylphosphine
    • Alias PhosPhine, isopropyldiphenyl-
    • Einecs 239-018-0
    • 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
    VTB
    Specifications

    HS Code

    697647

    Chemical Name Isopropyldiphenylphosphine
    Cas Number 2551-55-9
    Molecular Formula C15H17P
    Molecular Weight 228.27 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥97%
    Boiling Point 155-157°C at 2 mmHg
    Density 1.045 g/cm³ at 25°C
    Refractive Index n20/D 1.592
    Solubility Insoluble in water; soluble in organic solvents (e.g., toluene, ether)
    Flash Point 146°C
    Ec Number 219-860-9
    Synonyms Di(phenyl)isopropylphosphine, (Isopropyl)diphenylphosphine
    Storage Conditions Store under inert atmosphere, away from moisture and air

    As an accredited Isopropyldiphenylphosphine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Isopropyldiphenylphosphine is supplied in a 100-gram amber glass bottle, tightly sealed, with hazard labeling and chemical identification.
    Shipping Isopropyldiphenylphosphine should be shipped in tightly sealed containers, protected from light and moisture. Use appropriate chemical-resistant packaging and clearly label as a hazardous material. During transport, ensure compliance with local and international regulations for hazardous chemicals. Handle with care to avoid leaks or spills, and include proper documentation and safety information.
    Storage Isopropyldiphenylphosphine should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Store in a cool, dry, and well-ventilated area away from sources of moisture, heat, and incompatible substances such as oxidizers and strong acids. Protect from light and ensure appropriate spill containment and labeling in accordance with chemical safety regulations.
    Application of Isopropyldiphenylphosphine

    Applications of Isopropyldiphenylphosphine in Industrial Manufacturing

    Isopropyldiphenylphosphine plays a critical role as a speciality phosphorus-containing ligand and intermediate across several advanced chemical manufacturing segments. Below, we outline verified downstream applications tailored to the material’s unique properties, providing essential technical and regulatory context for professional users in the global industrial sector.

    1. Catalyst Ligand for Homogeneous Hydrogenation in Fine Chemical Synthesis

    The product is widely adopted as a monodentate ligand in transition metal-catalyzed hydrogenation processes, particularly in the synthesis of fine chemicals and intermediates for pharmaceuticals. It contributes to adjusting the electron and steric environment of the metal center for improved selectivity and reaction rates, and is preferred in scenarios requiring robust handling and fine-tuning of catalyst performance for complex molecule assembly.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA for intermediates)
    • EU EudraLex Vol 4, Part II (APIs and critical intermediates)
    • ISO 9001:2015 (Quality Management Systems for Chemical Manufacturing)

    Typical usage ratio

    • Ligand:metal molar ratios typically between 1.5:1 and 5:1, adjusted according to substrate steric requirements, catalyst activity, and batch vs. continuous flow system parameters.

    Downstream process integration

    • Added at the catalyst pre-complexation step, blending with metal (e.g., rhodium, ruthenium) salts prior to introduction of substrates and hydrogen in the reactor vessel.

    Final product types

    • Chiral alcohols for pharmaceutical actives
    • Fine chemical intermediates (amines, esters, carboxylic acids)
    • Agrochemical intermediates for crop protection
    • Speciality flavors and fragrance compounds

    2. Intermediate for Synthesis of Functionalized Phosphine Ligands

    Downstream producers use our material to construct a range of custom phosphine ligands required for catalytic processes and electronic-grade chemical manufacturing. The reactivity of the isopropyl group and aromatic rings provides a versatile starting point for selective functionalization, allowing high-value downstream ligand variants with defined electronic and steric profiles for demanding applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (EU substance registration)
    • ISO 14001:2015 (Environmental Management in chemical synthesis)
    • TSCA Inventory Listing (USA)
    • RoHS 2 (2011/65/EU, electronics industry use)

    Typical usage ratio

    • Reactant proportions typically in stoichiometric quantities, with excess up to 10% depending on the targeted ligand modification route (alkylation, aryl exchange, oxidation).

    Downstream process integration

    • Feeds into functionalization steps such as selective halogenation, sulfonation, or alkylation to produce application-specific phosphine ligands. Reaction sequence and protection strategies depend on final end-use requirements.

    Final product types

    • Phosphine-based ligands for cross-coupling catalysts (e.g., Buchwald-type)
    • Ligand systems for olefin polymerization catalysts
    • Electronic-grade organophosphorus compounds
    • Custom ligand libraries for asymmetric catalysis

    3. Organophosphorus Precursor for Synthesis of Fire-Resistant Materials

    Industrial formulators exploit the phosphorus center of our material as a building block to introduce fire-retardant characteristics into polymer matrices. The conversion to phosphine oxide derivatives delivers enhanced flame resistance by promoting char formation and disrupting combustion cycles in engineered plastics and coatings, contributing directly to compliance with safety requirements in construction and electrical appliance manufacturing sectors.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics)
    • IEC 60695 (Fire Hazard Testing for Electrical Devices)
    • REACH Annex XVII restrictions for halogenated flame retardants (EU)
    • NFPA 701 (Textile Flammability, USA)

    Typical usage ratio

    • Precursor charged at levels corresponding to 0.5–3.5 wt% phosphorus in the final composite, subject to base resin type and performance targets for flame resistance without diminishing mechanical strength or processing fluidity.

    Downstream process integration

    • Incorporated into resin blending steps as a phosphorus source, followed by thermal or oxidative conversion to phosphine oxide, prior to compounding with polymer base and co-additives in extrusion or molding stages.

    Final product types

    • Fire-resistant polycarbonate panels
    • Glass fiber reinforced thermoplastics
    • Protective industrial coatings
    • Safety-standard electrical housings

    4. Precursor for Organophosphorus Reagents in Agrochemical Synthesis

    Agrichemical producers use the compound as a platform intermediate to synthesize specialty phosphorus reagents, especially for organophosphorus herbicide and pesticide development. The customizable reactivity of the phosphine allows downstream chlorination, oxidation, or alkylation to manufacture agrochemical actives and intermediates where precise phosphorus incorporation is required.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO GAP)
    • ISO 9001:2015 (Agrochemical Synthesis Management)
    • OECD Guidelines for the Testing of Chemicals
    • China GB 4839-2009 (Pesticide Formulation Standards)

    Typical usage ratio

    • Used at stoichiometric or slight excess levels versus halogenating or oxidizing agents, with 1.0–1.2 equivalents typical for targeted functional group conversion and yield maximization.

    Downstream process integration

    • Feeds into phosphorus reagent preparation stages prior to incorporation in active ingredient synthesis—common reactions include controlled oxidation to phosphine oxides or esterification for subsequent use in pesticide formulation chains.

    Final product types

    • Phosphonate-based herbicides
    • Organophosphorus insecticide intermediates
    • Pesticide synergist additives
    • Seed treatment chemistry

    5. Modifier in High-Performance Polymer Manufacturing

    Performance plastic manufacturers utilize our isopropylphosphine derivatives to fine-tune the molecular weight distribution, melt-flow properties, and thermal stability of specialty polymers. The unique steric hindrance and electron-donating capacity of the isopropyl-aryl phosphine structure supports polymer chain termination control in high-temperature and specialty engineering polymers.

    Industry compliance standards

    • ISO 11357 (Differential Scanning Calorimetry for Polymers)
    • ASTM D638 (Tensile Properties of Plastics)
    • RoHS 2 (Restriction of Hazardous Substances for electronics plastics)
    • REACH (EC) No 1907/2006 compliance for plastics additives

    Typical usage ratio

    • Modifier loading levels typically in the 0.01–0.1 mol% (monomer basis), balancing required polymer architecture modification while maintaining finished product mechanical profiles—final ratio determined by polymerization kinetics and end-user specification.

    Downstream process integration

    • Introduced during monomer feed or early-catalyst stage of polymerization reactors; homogeneously mixed to achieve chain structure modifications prior to devolatilization and pelletizing.

    Final product types

    • Polyphenylene sulfone (PPSU) resins
    • Electronics-grade polyimide films
    • Engineering plastics used in automotive and aerospace sectors
    • Heat-resistant wire and cable insulation materials
    Free Quote

    Competitive Isopropyldiphenylphosphine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Insight into Isopropyldiphenylphosphine: A Manufacturer's Perspective

    The Role of Isopropyldiphenylphosphine in Modern Chemistry

    From our vantage point inside a chemical manufacturing facility, the story of Isopropyldiphenylphosphine starts at the intersection of real-world need and precision chemistry. Years of experience in organophosphorus synthesis revealed a gap: researchers and industrial producers alike wanted a phosphine ligand with predictable reactivity and reliable batch-to-batch consistency, capable of standing up to today’s rigorous catalytic processes. This isopropyl-modified diphenylphosphine brought the answer—a carefully structured molecule ideal for fine chemical synthesis, transition metal catalysis, and the pharmaceutical sector’s challenging demands.

    In the day-to-day, we see chemists selecting reagents that shave time from purification, cut costs, or make it possible to access previously unobtainable reaction intermediates. Isopropyldiphenylphosphine, produced in our reactors, jumps out by offering a clear advantage for those working with palladium, nickel, or ruthenium complexes. Its isopropyl substitution creates a unique balance between steric hindrance and electronic donation, giving rise to metal complexes with distinctive reactivity compared to more traditional triphenylphosphine or simple alkyl-diphenylphosphines.

    Experience Drives Production Choices

    Producing Isopropyldiphenylphosphine at scale is not a trivial operation—and familiarity with the process guards against the quality slippages that frustrate users. Experience shows that controlling air and moisture exposure during synthesis and packaging is essential, as common phosphines undergo rapid oxidation, which sabotages their performance. The expertise we deploy draws directly from repeated synthesis runs and close monitoring of each batch's spectral purity. We commonly ship material as a white to faintly yellow crystalline solid—a sign of both purity and careful process control. Sometimes a faint aromatic odor tells us the phosphine ring remains intact, confirming that degradation has not crept in.

    Finished product is regularly tested with both nuclear magnetic resonance and gas chromatography, not only to confirm purity above the typical 98 percent, but also to verify that trace impurities, which sometimes lurk below threshold detection, have been kept at bay. This insistence on rigorous quality isn’t about chasing certificates—it’s driven by a clear understanding that even slight deviations risk fouling a customer’s catalytic reaction or introducing variables that waste precious time and resources, both in pilot and full-scale manufacturing.

    Specifications Shaped by Practical Application

    Over years of dialog with partners across research labs and process chemistry departments, we’ve watched preferences and requirements evolve. In real reactions, even a variation in melting point or solubility profile carries consequences. Isopropyldiphenylphosphine should dissolve readily in most aromatic and aliphatic solvents, including toluene and tetrahydrofuran; achieving this solubility profile is not automatic. Fine-tuning the synthetic route, adjusting workup and crystallization parameters, and keeping an eye on trace byproducts all play a role in delivering a consistently handling product.

    Storage and handling recommendations also tally with what’s observed in the field. Users with bench-scale or bulk needs keep phosphine ligands under inert atmosphere—usually argon or high-purity nitrogen—in tightly sealed bottles. Stability varies among phosphines; Isopropyldiphenylphosphine regularly proves less prone to discoloration and decomposition compared with more electron-rich or sterically hindered alternatives. That stability means less wasted product and lower clean-up costs after scale-up experiments—tangible benefits for formulators and process engineers alike.

    Where Isopropyldiphenylphosphine Differentiates Itself

    There are many choices on the market for phosphorus ligands. From the outset, we were aware that Isopropyldiphenylphosphine answers a specific call in the catalyst toolbox. The isopropyl group, attached to phosphorus alongside two phenyl rings, brings a tweak in both steric and electronic character. Laboratory experience points to more selective activation of certain metal centers, especially during cross-coupling and hydrogenation reactions. Substitution with isopropyl creates a ligand with a tighter cone angle and updated bite angle, which impacts the reactivity of the downstream metal complex in subtle and sometimes dramatic ways.

    Colleagues working with triphenylphosphine or dicyclohexylphosphine have often relayed issues with inconsistent yields or byproduct formation in catalytic cycles. Isopropyldiphenylphosphine walks a middle path—its intermediate bulkiness suppresses enzyme-like side reactions while leaving enough room so that bulky substrates and reactants do not get crowded out. In pharma projects and academic test cases, the switch from phenyl or cyclohexyl analogues to isopropyl-diphenyl variants has proven decisive, knocking down unwanted rearrangements or competing side products.

    Supporting Users from Pilot Batches to Full-Scale Production

    We measure success by the feedback loop between our production floor and the chemists using the finished product. Product managers and synthetic chemists relied on us repeatedly for tight delivery timetables, specialized packaging, and clean transfer of bulk phosphine ligands. Issues rarely arise with shelf life, owing to our equipment upgrades and use of specialty-grade glass and polymers for storage. Over the past year, multiple pharmaceutical process teams reported an increase in catalytic yields and fewer operational surprises after transitioning to Isopropyldiphenylphosphine—evidence that deliberate improvements pay off across the production chain.

    Environmental stewardship guides both process design and packaging decisions. Our recycling system retrieves all phosphorus waste for downstream recovery, and our workforce routinely audits storage and containment for leaks, given the material’s sensitivity. Feedback from regulatory teams and customer health & safety officers shapes the information we deliver and the way we construct shipment sets. By integrating this information flow, we help chemists avoid the costly scenario of product loss or wastage due to improper handling, unexpected exposure, or breakdown during shipping.

    Application in Catalytic Systems and Special Synthesis Tasks

    A steady stream of use-cases arrives each year, confirming the versatility of Isopropyldiphenylphosphine in organometallic catalyst design. In Heck, Suzuki-Miyaura, or Buchwald-Hartwig couplings, chemists note marked improvement in both selectivity and turnover number after swapping in this ligand. The isopropyl group tempers the electron-donating nature of the phosphorus atom, boosting metal-ligand bond strength while maintaining enough flexibility for catalytic cycles that demand repeated oxidative addition and reductive elimination. For those working in electronic materials, the stability of this ligand also enhances the purity of functionalized aryl or heteroaryl products, yielding cleaner reaction profiles and easier downstream purification.

    Scale, too, creates its own set of challenges. What works at a flask level seldom translates seamlessly to the pilot plant. Our team saw early on that several commercial ligands, including triphenylphosphine analogues, break down or foul metal surfaces after repeated runs. With Isopropyldiphenylphosphine, maintenance techs noted fewer issues with clogged reactors, blocked filters, or erratic catalyst poisoning, freeing process engineers to optimize for output instead of chasing down contamination events. We have also supplied bulk quantities for agricultural and custom polymer synthesis, where its balanced properties improve catalytic throughput and reproducibility over older phosphine generations.

    Viewpoint from Long-Term Manufacturing Practice

    From the beginning, we appreciated that subtle shifts in ligand architecture can produce outsize effects in downstream chemistry. Our process controllers spotted persistent issues with oxygen ingress in older packaging designs, which we solved by adopting improved inerting and container sealing methods. Years spent cleaning out reactors after “regular” diphenylphosphine runs have shown that every increment of stability in the ligand translates directly into less cleaning labor and downtime. Scale-up teams, often working double shifts, favor any improvement that staves off batch-to-batch inconsistency or unplanned rework cycles in pharma intermediates or specialty polymers.

    User education comes as part of the job; the subtleties of handling phosphorus-based reagents do not always appear obvious, especially to teams new to fine chemical synthesis. Regular technical exchanges and frank error reporting keep failure rates low and help our clients maximize value for each kilogram purchased. In recent years, as process audits sharpened and regulatory burdens increased, robust documentation around Isopropyldiphenylphosphine storage and shelf life has served end-users well. There’s a straightforward benefit in having a long-standing partnership between laboratory, production, and quality assurance.

    Comparisons Beyond the Catalog Page

    It’s tempting to line up candidate ligands by melting point, solubility, and price—then pronounce a winner. Decades working with phosphorus-based reagents have demonstrated that decision-makers benefit more from lived experience: which ligand withstands repeat heating cycles, which one leaves fewer residues on reactor walls, which batch delivers tighter selectivity at the highest scale. Isopropyldiphenylphosphine slots in as a reliable midpoint between more hindered species, such as di-tert-butylphosphines, and leaner, more electron-rich compounds. This balance makes it a favorite among users struggling with difficult couplings or seeking to enforce a stubborn selectivity plateau in their product line.

    Comparing direct competitors, the ligand’s isopropyl substituent brings a slightly greater steric bulk than ethyl or methyl analogues, yet remains shapable enough for rapid metal insertion-de-insertion cycles. Industrial users, particularly in continuous processes and flow chemistry modules, see greater lifetime performance for precious metal complexes—slower ligand dissociation, fewer episodes of catalyst bleed, and improved material efficiency per reaction volume.

    Customer-Driven Innovation and Collaborative Dialogue

    Time and again, true progress has followed collaborative troubleshooting. Routinely, partners approach us after encountering degraded yields with more cost-driven phosphines supplied by brokers or spot-shipped from variable sources. We’ve seen, across hundreds of production and pilot campaigns, that stable, high-purity Isopropyldiphenylphosphine lowers out-of-spec material incidents, and the accumulated cost savings ultimately outweigh the perceived price difference. With ongoing improvements in synthesis protocols, waste reclamation, and finished product verification, customers gain the reassurance that each shipment performs consistently—whether deployed at milligram, kilogram, or multi-ton scale.

    Active listening, not just monitoring numbers, shapes how we optimize our process and recommend variants for tailored reactions. Specialists in active pharmaceutical ingredient synthesis, for instance, shared positive results regarding enantioselective transformations, with reportable gains in yield for certain chiral ligation steps using our isopropyl-bearing ligand. There are also cases from the electronics sector, where minute differences in ligand performance have direct impact on device purity and operational lifetime. The multiplication of such stories across fields confirms that attention to user experience—borne out by repeat testing and follow-up—beats a generic “one-size-fits-all” approach.

    Facing Practical Challenges in Handling and Supply Chain

    Continuous improvement in shipping and quality management remains a central pillar of our operation. Feedback from distributors pointed to rare but costly incidents during extreme weather or shipping delays, prompting us to revamp insulation protocols for larger shipments. Retaining stability even under variable warehouse lighting or temperature swings has earned Isopropyldiphenylphosphine a spot among frequently re-ordered catalog entries, both locally and for overseas customers. We encourage open discussions with freight handlers and warehouse teams, because phosphine ligands—stable though they may be when pure—can degrade quickly if mishandled at any point from packaging to delivery.

    We’ve personally seen the benefits, and the potential pitfalls, when clients branch out to new synthetic routes involving this ligand. Mistimed solvent charges, unexpected temperature deviations, or impurities from aging catalyst stocks have all been traced back by our technical team to root causes. Direct input from us—delivered through on-site training, white papers, and helpline support—bridges the gap from factory to laboratory. Over time, we found that early, honest engagement cuts downtime related to troubleshooting and helps customers unlock the full potential of the material, whether the project involves custom catalyst development, new monomer synthesis, or pilot polymerizations.

    Looking Ahead: Sustainable Practices and Market Evolution

    Responsible manufacturing means investing in greener chemistry, replacing outdated or unsafe solvents, and minimizing energy elsewhere in the process. Growing demand for environmentally friendly ligands has prompted a thorough review of every step of Isopropyldiphenylphosphine’s manufacture—from choice of phosphorus precursor and control of reducing agents, to internal recycling of waste streams. In collaboration with green chemistry advocates, we have trialed alternative reducing agents, recovered mother liquors, and worked to minimize the use of volatile organics.

    Customer audits push us to document and improve every year. Calls for data on emissions, worker exposure, and lifecycle risks flow in from compliance officers and downstream buyers. Sharing real-world performance data helps customers fulfill their own compliance requirements—especially important in the pharmaceutical and agrochemical sectors, where transparency on sourcing and batch history is non-negotiable. Our investment in process control and continuous analytics places us in a strong position to guarantee traceability and reliable supply, even as regulations shift or market dynamics tighten.

    Why Isopropyldiphenylphosphine Holds a Place in Inventive Chemistry

    With decades on the floor, we have witnessed the progression from simple commodity phosphines toward specialized ligands that open new synthetic spaces. Isopropyldiphenylphosphine typifies this shift—carrying features that appeal equally to the process engineer scaling up an agricultural intermediate and the academic researcher probing a new metal-catalyzed pathway. Our commitment to transparent, open exchange with our partners and customers has created a cycle of trust and technical progress that far outlives any individual batch or order. Each improvement in purity, stability, and shipping reliability creates direct value for those pushing the boundaries of synthesis.

    Reflecting back, the story of Isopropyldiphenylphosphine in our facility is not just about molecules. It encompasses teamwork among analytic chemists, process specialists, logistics professionals, and customer technical support, all moving with a shared aim: produce a reagent so dependable that the only surprises are the creative discoveries chemists uncover with its help. From the early days of challenging reaction cycles, through years of customer collaboration and iterative improvement, this ligand has carved out its place within the modern chemist’s toolkit, ready for whatever tomorrow’s chemistry brings.