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1,2-Bis(Dichlorophosphino)Ethane

    • Product Name 1,2-Bis(Dichlorophosphino)Ethane
    • Alias 1,2-Bis(dichlorophosphino)ethane
    • Einecs 252-219-5
    • 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

    863330

    Chemicalname 1,2-Bis(dichlorophosphino)ethane
    Casnumber 14647-64-8
    Molecularformula C2H4Cl4P2
    Molecularweight 249.81 g/mol
    Appearance Colorless to pale yellow liquid
    Meltingpoint -22 °C
    Boilingpoint 220 °C (decomposes)
    Density 1.609 g/mL at 25 °C
    Solubility Decomposes in water, soluble in organic solvents
    Refractiveindex 1.544 at 20 °C
    Purity Typically >97%
    Synonyms Ethylene bis(dichlorophosphine)
    Flashpoint Greater than 110 °C
    Storagetemperature Store under inert gas, 2–8 °C
    Ecnumber 238-686-7

    As an accredited 1,2-Bis(Dichlorophosphino)Ethane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2-Bis(Dichlorophosphino)Ethane, 25g, is packaged in a sealed amber glass bottle with a secure screw cap, labeled for laboratory use.
    Shipping 1,2-Bis(Dichlorophosphino)ethane is shipped in tightly sealed containers under inert gas, typically argon or nitrogen, to prevent moisture and air contact. Containers must be labeled according to hazardous material regulations and handled with care as the chemical is moisture sensitive, corrosive, and toxic. Store and transport at controlled room temperature.
    Storage **1,2-Bis(Dichlorophosphino)ethane** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis. Keep in a cool, dry, and well-ventilated area away from moisture, air, and incompatible substances (e.g., strong oxidizers). Store in a chemical fume hood and label appropriately as it is moisture-sensitive and potentially hazardous.
    Application of 1,2-Bis(Dichlorophosphino)Ethane

    Applications of 1,2-Bis(Dichlorophosphino)Ethane in Industrial Manufacturing

    1,2-Bis(Dichlorophosphino)ethane has established itself as a highly specialized intermediate in fine chemical synthesis, especially for downstream sectors with strict purity and process requirements. As a manufacturer, we highlight key application segments where this compound plays a critical role in industrial value chains.

    1. Homogeneous Catalysts Synthesis for Fine Chemicals

    This material serves as a ligand precursor for advanced metal catalyst systems, particularly in the design and production of chelating diphosphine ligands used with transition metals. Industrial catalyst formulators introduce it at the ligand preparation phase, converting it into bis(phosphine) derivatives, which further complex with metals such as nickel, palladium, or platinum. This step enables highly selective hydrogenation, hydroformylation, and carbonylation processes crucial to fine chemical output, including specialty alcohols, aldehydes, and acids.

    Industry compliance standards

    • ISO 9001:2015 certified production and QC
    • REACH Regulation (EC) No 1907/2006 registration for all synthetic ligands
    • IUPAC and ACS standards for ingredient identity and trace metal limits
    • Responsible Care® Process Safety guidelines

    Typical usage ratio

    • 5–15 mol% relative to target metal center; ratio depends on ligand:metal chelation geometry for desired catalytic activity

    Downstream process integration

    • Ligand functionalization precedes metal complexation step; added during inert atmosphere synthesis, prior to catalyst formulation

    Final product types

    • Rhodium and nickel-based diphosphine catalyst complexes
    • High-performance hydrogenation and isomerization catalysts
    • Specialty chemical process intermediates (alcohols, amines, acids)

    2. Organophosphorus Ligand Manufacture for Pharmaceutical Catalysis

    Pharmaceutical process chemistry employs this compound to prepare highly pure bisphosphine ligands for enantioselective and asymmetric catalytic steps. The material enters the ligand synthesis workflow requiring rigorous cGMP documentation, precise stoichiometry control, and validated trace impurity analysis to meet regulatory specifications essential for active pharmaceutical ingredient (API) manufacturing routes reliant on high-purity coordination chemistry.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and EP monograph-based ligand impurity controls
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • Annual third-party traceability audits

    Typical usage ratio

    • 0.5–2 equivalents per equivalent of transition metal precursor; adjusted based on required enantioselectivity and ligand backbone structure

    Downstream process integration

    • Bisphosphine synthesis and purification carried out before integration in API synthesis reactor train; tightly controlled in inert and anhydrous conditions

    Final product types

    • Chiral catalysts for pharmaceutical intermediates
    • Enantio-enriched alcohols, amines, and other API precursors
    • Ligand kits for custom pharmaceutical catalyst packages

    3. Coordination Polymer and Metal-Organic Framework (MOF) Precursor

    Specialist materials producers utilize this compound as a building-block ligand component in the formation of advanced coordination polymers and metal-organic frameworks (MOFs). It forms bridging diphosphine linkages with selected metal ions, enabling tuneable porosity and functionality. These advanced porous solids serve as supports, selective absorbents, and next-generation separation media in downstream industrial purification.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management Systems) for synthetic solids
    • REACH and CLP Regulation (EC) No 1272/2008 for precursor raw materials
    • ASTM E2409-13 for MOF characterization protocols
    • OECD guidelines for waste management in advanced materials processing

    Typical usage ratio

    • Stoichiometric ligand:metal ratio is typically 2:1 or tailored to framework topology; modified to control polymer morphology

    Downstream process integration

    • Bisphosphine precursor introduced during MOF or coordination polymer self-assembly in solution-phase synthesis; afterwards, solid-state post-processing and activation steps follow

    Final product types

    • Catalytically active MOFs for process gas separation
    • Adsorbent solids for fine chemical and petrochemical purification
    • Functionalized coordination polymers for membrane applications

    4. Flame Retardant Intermediate for High-Performance Polymers

    Specialty polymer manufacturers use this chemical as a phosphine-based intermediate, converting it into stable, phosphorus-containing monomers. These integrate into advanced polymer chains in order to boost flame resistance and smoke suppression in demanding industrial environments. Its role in achieving reliable polymer backbone modification complies with mandatory fire safety and material certification testing for electronic components, transport interiors, and construction panels.

    Industry compliance standards

    • UL 94 and IEC 60695 (Fire hazard testing for plastics)
    • EN 45545-2 (European railway fire protection standard)
    • ISO 1043-4 (phosphorus-based additives in plastics)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electrical and electronic equipment)

    Typical usage ratio

    • Phosphine-derived intermediate constitutes 2–8 wt% of final polymer blend, tuned according to target V-0/UL flame resistance performance and mechanical properties

    Downstream process integration

    • Converted via phosphination and polycondensation into phosphorus-modified monomers, incorporated during melt blending or extrusion of engineering thermoplastics, ensuring homogeneous phosphorus distribution

    Final product types

    • Flame-retardant polyesters and polyamides
    • Low-smoke emission cable insulation materials
    • Composite panels for aerospace and rail uses

    5. Custom Ligand Production for Petrochemical Catalysis

    Refinery and petrochemical technology suppliers select this compound to generate specific bidentate ligands for the formulation of proprietary catalytic systems. These systems drive key transformations in hydroformylation, alkene oligomerization, and selective olefin conversion units. The raw material’s integration into ligand synthesis protocols follows process safety standards and delivers reliable batch-to-batch reproducibility.

    Industry compliance standards

    • API Process Safety Management (PSM) guidelines
    • ASTM D849 for catalyst evaluation in refinery processes
    • REACH compliance for bulk chemical catalyst constituents
    • Company-specific document control under ISO 9001:2015

    Typical usage ratio

    • Ligand dosage tailored from 0.2–2 mol% of feedstock, with adjustment based on hydroformylation or oligomerization reactor conditions

    Downstream process integration

    • Bidentate phosphine introduced at the catalyst blending step; full ligand synthesis and metal salt combination conducted under anoxic, pre-activation protocol to protect against oxidation

    Final product types

    • Bulk α-olefins (C4–C20)
    • Oxo-alcohols for downstream plasticizer manufacture
    • High-value synthetic lubricants
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    Certification & Compliance
    More Introduction

    Introducing 1,2-Bis(Dichlorophosphino)Ethane: A Chemist’s Workhorse for Advanced Synthesis

    Stepping Into Precision: Our Experience with 1,2-Bis(Dichlorophosphino)Ethane

    For years on the production floor, I have watched the progress of phosphine ligands from a backroom curiosity in catalyst research into the mainstay chemicals they are today. There is little substitute for practical experience with these compounds, especially when purity, reactivity, and long-term consistency matter to real-world users. Among these, 1,2-Bis(Dichlorophosphino)Ethane grabs attention for the difference it makes in modern complex synthesis.

    This molecule—often recognized by chemists as 1,2-bis(dichlorophosphino)ethane or simply “DPPE-Cl2”—features a two-carbon ethylene backbone with a dichlorophosphino group at each end. The result is a bidentate ligand that supports a range of transition metal catalysts, from platinum and nickel to rhodium. Its simplicity is deceptive. Real utility comes from the combination of bite angle, electron-donating characteristics, and reliable handling. For colleagues in the chemical industry, this is no fringe reagent. It’s a backbone of cleaner, more tailored complex formation and a cornerstone for targeted organometallic synthesis.

    The Nuts and Bolts: Model, Quality, and What Sets DPPE-Cl2 Apart

    Our standard batch is produced consistently as a colorless to faintly yellowish liquid, known for pungency and notable air sensitivity. We keep the content above 99% purity by area using gas chromatography, and aim for a moisture readout under 500 ppm. This attention to water avoidance stands front and center in our workflow. Minute traces of water or oxygen kick off side reactions that tank yields downstream, especially when preparing metal complexes for high-stakes catalysis. These are not numbers plucked from specs; they come out of years keeping the vacuum lines in perfect order, glassware bone-dry, and gas purges flowing.

    Working at scale sharpens focus. DPPE-Cl2 requires constant care—another detail separating a specialty manufacturer from repackaging brokers. Small variations in pressure and temperature during synthesis leave marks in impurity profiles. We keep production strictly in gloveboxes or under nitrogen, never trusting ambient air to maintain integrity. Our customers measure performance in the ease of downstream handling, lack of hydrolyzed by-products, and repeatable results batch-to-batch. In-house, routine titration tracks the P–Cl content, with phosphorus NMR as our daily check for molecular symmetry and unwanted formation of mono-substituted byproducts.

    Where DPPE-Cl2 Goes to Work—and Why Chemists Return

    Ask any synthetic chemist why DPPE-Cl2 stays on the order form, and the answer will circle back to versatility. This molecule stands as the go-to building block for preparing bisphosphine ligands. These ligands are crucial in coordinating with transition metals for homogeneous catalysis—hydroformylations, carbonylations, and asymmetric hydrogenations depend on them. More specifically, 1,2-bis(dichlorophosphino)ethane opens doors to making the much-used DPPE and its derivatives, which sport a huge influence on reaction selectivity and catalyst stability.

    In real manufacturing, customers use DPPE-Cl2 as a precursor, modifying it with various Grignard or organolithium reagents. The robust P–Cl bond is reactive enough to allow controlled substitution, but predictable and manageable in skilled hands. This reliability stands above most monodentate analogs, where unwanted side reactions throw off the stoichiometry and foul up complex assembly. Compared to 1,3-dichloropropane-based frameworks, the two-carbon DPPE backbone delivers a more manageable bite angle, often translating to stronger, more predictable chelation for platinum group metal catalysts.

    We see a lot of this material shipped to specialty labs and pilot plants working on the next cycle of agrochemical and pharmaceutical actives. Ligand libraries built from this core continue to set research announcements, especially where chirality and stereoselectivity step into the foreground. The product’s clarity and minimal inclusion of residual hydrocarbon byproducts are what bench chemists cite in feedback. In an environment where every degree of selectivity means dollars in the process yield and purity, those small differences stack up fast.

    The Real-World Differences: DPPE-Cl2 vs. Other Chlorophosphines

    Through the eyes of both operator and end-user, choosing a dichlorophosphinoethane over monodentate chlorophosphines or longer-chain versions is not just a matter of preference. Most single-phosphorus chlorophosphines, such as chlorodiphenylphosphine, can serve in introducing phosphorus into organic or organometallic frameworks, but the chemoselectivity and control over chelation they offer is limited. Coordination chemistry rewards precision in ligand geometry. With DPPE-Cl2, the chelation geometry is hard-wired; both phosphorus atoms anchor at fixed intervals. This direct control leads to sharper ligand field effects and allows researchers to maintain identical electronic surroundings between the two phosphorus centers when constructing symmetric complexes.

    Extended backbones—say, 1,3- or 1,4- systems—push the phosphorus groups farther apart. This alteration looks minor in a textbook, but in the lab, those extra methylene units disrupt the chelate ring size and the resulting metal-ligand dynamics. Years of catalysis screening show that the two-carbon system leads to more robust, thermally stable complexes, both for industrial hydrogenation and for high-value synthesis in pharma or fine chemicals. It’s a lesson taught by failed yields and unexplained by-products—something the manufacturing community recognizes after enough cycles making and breaking these bonds.

    Another place DPPE-Cl2 excels is shelf stability, granted the material sees careful packaging. We dedicate time to purging containers with inert gas, double-bagging under nitrogen, and confirming moisture content before shipment. Customers still using older in-house syntheses often mention inconsistent color or a faint haze—reliably avoided in our newest output thanks to refined dehydration protocols and careful storage. The product’s sharper, well-defined NMR signals also stand as a testament to consistent purity.

    Eyes on Safety and Scalability: Manufacturer’s Perspective

    DPPE-Cl2 is not "plug and play" for every environment. Our team deals daily with its clear hazards—fuming on contact with air, strong corrosiveness, and acute toxicity. These aren’t theoretical issues; one misstep means evacuation and a hard lesson in emergency protocol. We commit to hard-won safety practices, keeping engineering controls robust, automating as much transfer as possible, and using positive-pressure personnel protection for every large-scale operation.

    On the scalability front, efficiency in phosphorus utilization matters as prices for elemental phosphorus climb and regulations encircle every stage. We reduce waste streams by using closed-loop capture of evolved by-product gases and optimize our quench protocols to minimize chlorinated effluent. These efforts are not about ticking sustainability boxes—they direct costs lower and keep manufacturers ahead of tightening regulatory scrutiny. The investment in state-of-the-art reactors pays back not only in purity, but in throughput, allowing for consistent multi-hundred-kilogram and up batches while delivering the repeatable performance leading customers demand.

    Handling and Storage: Lessons from Years in the Field

    Regular users of DPPE-Cl2 know that storage is more than just keeping a drum in the dark. The compound’s moisture sensitivity means even small lapses in packaging or atmosphere control translate to extra purification steps and lost material downstream. We recommend opening each bottle inside a glovebox or beneath a nitrogen or argon stream, quickly transferring the required dose, and resealing immediately. Our packages ship with visual indicators and accompanying desiccants to provide real-time alerts for breaches—knowledge picked up from feedback reaching all the way from startup labs to multi-national licensors.

    From our own mishaps in early days, the wisdom has become routine: maintain tight control over handling, triple-check seals, and never risk using a container that shows even a hint of separator breakdown. A product spoiled by humidity not only risks the next reaction but could introduce trace byproducts that only reveal themselves under NMR or after late-stage failures. These lapses translate to lost batches, urgent calls to suppliers, and expensive remediation—not theoretical, but logged as hard experience.

    Supporting Innovation: DPPE-Cl2 as a Link to the Next Generation of Chemistry

    Our production lines may appear old-fashioned, but the real work happens at the molecular interface. DPPE-Cl2 delivers the power to rapidly customize ligand frameworks as research directions evolve. Pharmaceutical teams harness these ligands for chiral induction in API synthesis, advancing medicines that target previously unreachable biological mechanisms. Agrochemical research banks heavily on rapid iteration through ligand libraries—DPPE-Cl2 acts as a universal foundation, supporting everything from herbicide development to more selective pesticide pathways.

    Innovation thrives on reliability. A product that varies even fractionally in phosphorus content from batch to batch slows research, throws off results, and costs time. Our feedback channel remains open to process engineers and lab directors who point out the difference between a dry, colorless liquid and an off-hue material that signals oxygen or moisture exposure. Years of conversation with end-users teach us that documented traceability, rapid fulfillment, and on-demand technical support mean as much as the product’s specs themselves.

    Adaptation and Solutions: Navigating Evolving Challenges in Synthesis

    Environmental regulations and labor shortages continue to reshape chemical manufacturing. Our site has weathered stricter reporting and increasingly complex transport rules on chlorinated and phosphorus-containing compounds. In response, every release comes with full documentation—batch chromatograms, phosphorus NMR spectra, and certificates of water content—giving customers the security regulators expect without slowing research or delaying production.

    Customers working at scale often ask for guidance combining DPPE-Cl2 with in-situ process monitoring. We offer application advice refined by our own troubleshooting: keep backgrounds dry, avoid over-dilution, and stagger additions to reduce local heat spikes during phosphine incorporation. Direct communication between manufacturer and user—cutting out agency intermediaries—keeps these details accurate and actionable.

    One area where we’ve innovated involves shipping. Requirements change depending on destination, so we upgrade packaging and ship under screened logistics partners, guaranteeing materials arrive uncompromised. Our technical team actively tracks transit temperatures and humidity and remains ready to support cargo troubleshooting in real-time.

    Looking Ahead: 1,2-Bis(Dichlorophosphino)Ethane as a Foundation for Further Growth

    From a production plant perspective, 1,2-bis(dichlorophosphino)ethane’s role continues to expand. Markets in Asia and the Americas now account for most of the usage, driven by high-demand industries in smart materials, electronics, and pharmaceutical fine chemicals. As the need for specialized catalysts and tighter control over molecular architecture only increases, demand for robust, predictable bidentate ligand precursors like DPPE-Cl2 grows in parallel.

    For users, it pays to select a manufacturer experienced in every link of the supply chain—one who relies on strict chlorination control, cold transfer, sealed handling, and rigorous batch analytics. Adapting to customer workflows, supporting scale-ups, and responding fast to changing research needs remain central to our philosophy. DPPE-Cl2 may not be glamorous, but its reliability underpins everything from Nobel-winning chemistry to everyday industrial processes. Its ongoing story gets written each day on our lines, and in the breakthroughs of those who depend on it.

    Summary: Shaping Better Chemistry with DPPE-Cl2

    From our vantage as a direct manufacturer, the story of 1,2-bis(dichlorophosphino)ethane shows few shortcuts and plenty of lessons. Every batch reflects hard-won improvements—sharper purity, safer handling, more consistent output. For research, manufacturing, and downstream development, the product’s rigor enables sharper science and more confident scale-up. That reliability does not come by accident; it results from daily experience, strict control, and a continuous feedback loop with real customers solving real problems. DPPE-Cl2 will stay at the center of innovation so long as chemistry keeps pushing boundaries and manufacturers dedicate themselves to meeting the challenge.