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1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride

    • Product Name 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride
    • Alias IPr·HCl
    • Einecs 620-352-8
    • 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

    321959

    Productname 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride
    Casnumber 80873-04-3
    Molecularformula C27H36ClN2
    Molecularweight 423.04
    Appearance White to off-white solid
    Meltingpoint 205-210°C
    Purity Typically ≥98%
    Solubility Soluble in water and polar organic solvents
    Storagetemperature Store at 2-8°C
    Synonyms IMes·HCl, IMes imidazolium chloride
    Smiles CC(C)c1cccc(c1C(C)C)n2cc[n+](c2)c3c(C(C)C)cccc3C(C)C
    Inchikey PLSZHQNNVMSMBV-UHFFFAOYSA-M

    As an accredited 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 10g of 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride in a sealed amber glass bottle with safety labeling.
    Shipping 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride is shipped in tightly sealed containers, protected from moisture and light. It should be stored at room temperature in a dry, well-ventilated area. Proper labeling and documentation are required. Handle with gloves and safety goggles; avoid physical damage or inhalation during shipping and handling.
    Storage 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Handle under inert atmosphere, such as nitrogen or argon, to prevent decomposition. Ensure appropriate labeling and access only to trained personnel.
    Application of 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride

    Applications of 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride in Industrial Manufacturing

    As the direct producer, we supply 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride to downstream manufacturers who use this imidazolium-based ionic liquid in advanced material synthesis, catalysis systems, polymer modification, and battery technologies. With careful control of purity, consistency, and trace contaminants, we enable large-scale users to comply with regional and sectoral quality standards in their final product portfolios.

    1. Homogeneous Catalysis in Fine Chemicals Synthesis

    Chemical manufacturers incorporate this imidazolium chloride as a phase-transfer agent and ion carrier in homogeneous transition metal-catalyzed processes, particularly for C–C cross-coupling and alkylation reactions. The use of this salt enhances catalyst life, supports ligand stabilization, and fine-tunes ionic environments for high-value aromatic and pharmaceutical intermediates. In such processes, process engineers adjust dosage for each catalyst metal, solvent polarity, and product selectivity based on pilot trials and scaled runs.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • REACH Regulation (EC) No 1907/2006 compliance for substance registration
    • Pharmaceutical synthesis follows ICH Q7 GMP for active pharmaceutical ingredient (API) production, if relevant
    • Chemical handling and transport per GHS and national Hazmat directives

    Typical usage ratio

    • 0.5 mol% to 5 mol% relative to the primary metal catalyst in organometallic systems
    • Adjusted based on catalyst turnover frequency, solvent volume, and impurity profile

    Downstream process integration

    • Added during catalyst pre-charging or as an in-situ stabilizer before substrate introduction
    • Integrated in jacketed batch reactors or continuous flow reactors with inline mixing
    • Removed or recycled after post-reaction workup by aqueous extraction or selective distillation

    Final product types

    • Pharmaceutical intermediates (e.g., substituted aromatics, imidazoles, biaryls)
    • Fine chemical actives for agrochemical or specialty fragrance sectors
    • Brominated or alkylated aromatic building blocks

    2. Precursor for N-Heterocyclic Carbene (NHC) Ligand Manufacturing

    Specialty chemical plants utilize this compound as a core building block to synthesize NHC ligands for transition metal catalysis. The high steric protection given by the diisopropylphenyl groups on the imidazolium core enables consistent NHC precursor reactivity and robust ligand frameworks. Manufacturing sites deploy inline QC to ensure stoichiometric alkylation and minimize N-alkylation side-products across various NHC synthesis pathways.

    Industry compliance standards

    • ISO 17025 laboratory accreditation for analytical validation
    • Responsible Care global chemical sustainability principles
    • REACH substance process documentation including downstream user reports
    • Certificate of Analysis (CoA) to client specification for each lot

    Typical usage ratio

    • 1.0 equivalent relative to metallic alkoxide or base in NHC precursor synthesis
    • Small-scale reactions: stoichiometric; industrial: slightly (>1%) excess to drive full conversion

    Downstream process integration

    • Charged directly to jacketed reactors for quaternization or carbene formation steps
    • Product isolation via filtration, solvent exchange, and drying under vacuum
    • QC testing at each step for residual chloride and by-products

    Final product types

    • NHC ligand precursors for precious metal catalysts
    • Air-stable imidazolium-based NHC salts
    • Customized ligand intermediates for palladium, gold, copper catalytic processes

    3. Ionic Liquid Electrolyte for Energy Storage Cells

    Advanced battery companies formulate high-viscosity ionic liquid electrolyte blends using this material to improve safety and energy density in secondary lithium and sodium ion batteries. The sterically hindered cation structure delivers improved oxidation resistance and thermal stability, which are critical for next-generation solid-state and hybrid liquid–gel batteries aimed at stationary storage and high-power electronics markets.

    Industry compliance standards

    • UN38.3 battery testing for safety and transport qualification
    • RoHS 2011/65/EU for heavy metal and restricted substance content
    • IEC 62660 for automotive battery reliability
    • Material Traceability Documentation per ISO 9001:2015

    Typical usage ratio

    • 10–25 wt% of total electrolyte weight in blended mixtures with conducting salts (e.g., LiPF6, NaClO4)
    • Ratio adjusted depending on the desired viscosity, conductivity, and electrochemical window

    Downstream process integration

    • Direct blending with lithium salts and organic solvents under inert atmosphere in batch mixers
    • Pre-drying system to minimize water content below 20 ppm
    • In-line filtering and QC before cell filling and final assembly

    Final product types

    • Rechargeable lithium ion batteries (high-voltage or high-temperature grade)
    • Stationary sodium-ion battery modules
    • Electrochemical supercapacitors

    4. Stabilizing Agent in Specialty Polymer Synthesis

    Polymer manufacturers employ this imidazolium salt as a stabilizer and ionic additive in the synthesis of specialty polyelectrolytes and ion-exchange resins. Its bulky cation inhibits chain degradation and supports grafting processes during functionalization of engineering plastics, enabling higher molecular weight retention and uniform charge distribution required for advanced filtration or sensor applications.

    Industry compliance standards

    • ISO 14001 for environmental management in polymer production
    • FDA 21 CFR 177 for polymers in food contact, as required by end-use
    • REACH Annex XVII compliance for restricted substances in plastics
    • QC as per ASTM D638 (mechanical properties) and D792 (density determination)

    Typical usage ratio

    • 0.1–2.0 wt% in monomer blends or reactor charges
    • Ratio determined by required ionic concentration and polymerization mechanism (solution, suspension, emulsion)

    Downstream process integration

    • Introduced during monomer premixing or inline dosing to the polymerization reactor
    • Compatibility checked using solvent screening and pilot compounding trials
    • QC in extrudate or bead post-processing for residual chloride profiling

    Final product types

    • High-performance anion-exchange membranes (AEMs)
    • Functionalized polyimides for filtration modules
    • Sulfonated aromatic polymers for sensoring and separation applications
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    Competitive 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride: Experience from the Manufacturer's Viewpoint

    Our Perspective on an Essential Building Block

    For over two decades, our team has focused on the development and production of specialty imidazolium salts. Our experience with 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride reaches back to the early wave of research activity around N-heterocyclic carbenes (NHCs) and the rise in demand for air-stable, reliable precursors. We’ve seen the field transform as chemists have found new ways to leverage NHCs for organometallic synthesis, catalysis, and materials science. Through countless production runs, we learned how small changes in process can greatly influence product purity and performance in downstream applications.

    Consistent Quality at Scale

    The molecular structure may seem simple at first glance, but behind it lies a careful balance of steric and electronic properties. Our product, with its two bulky diisopropylphenyl groups flanking the imidazolium core, delivers across synthetic and practical needs. The chlorinated salt form we manufacture consistently meets expectations for reactivity and shelf stability, showing less sensitivity to moisture compared to some related halide or tetrafluoroborate NHC precursors.

    Over the years, we've refined our process to minimize color impurities and ensure a powder with high chemical purity—critical for applications such as the formation of sensitive organometallic complexes. Typical batches present as a white to off-white powder, checked by NMR, HPLC, and elemental analysis. In the lab, researchers have commented on improved solubility in acetonitrile and common organic solvents, allowing for easier handling and transfer during glovebox operations.

    Production Experience Meets Laboratory Needs

    Producing this imidazolium chloride at scale was not a trivial achievement. Early on, yields would vary, and controlling trace byproducts required close monitoring throughout synthesis and purification. We run high-purity toluene extractions, followed by careful recrystallization and drying techniques. All solvents get rigorously tested to prevent unwanted metal contaminants, which can interfere with sensitive downstream steps. We have invested in isolating pure product in ambient conditions without the usual trade-off of hydrolysis or decomposition, thanks to robust moisture control at each stage.

    We manufacture this compound with the needs of synthetic chemists front-of-mind. A research group recently shared feedback: Their glovebox set-up runs more smoothly because our packaging and stability reduce the frequency of impurity-cleansing steps. Over the years, we've seen time and again how inconsistent starting materials can create headaches in catalysis research, whether in the context of late-stage alkylations or metal-ligand complex formation. Scaling our process to serve kilo-lab and pilot plant users meant building redundancies into purification and supply chain management. Our technical staff document every lot’s characteristics and traceability, and major research consortia have relied on that transparency.

    Key Differences from Other Imidazolium Salts

    Not all NHC precursors are created equal. Some offer minimal steric protection, leaving metal centers susceptible to side reactions and decomposition. Others veer too far in the opposite direction—the ligand becomes physically obstructive, leading to sluggish reactivity and unwanted byproducts. Through hands-on experience with hundreds of synthesis campaigns, we find this 1,3-Bis(2,6-Diisopropylphenyl)imiazolium salt strikes a notable balance. The bulky isopropylphenyl wings protect the carbene, yet don't stifle reactivity or solubility in benchmark reactions. Researchers often compare its performance with common alternatives like 1,3-diisopropylimidazolium or 1,3-bis(mesityl)imidazolium salts. Our product’s fine-tuned steric and electronic profile pulls ahead during the synthesis of palladium or gold complexes—two workhorse metals in catalysis.

    Unlike some lower-cost ammonium and phosphonium salts, which break down at elevated temperatures or in the presence of trace water, our imidazolium chloride offers both high decomposition temperatures and robust resistance to hydrolysis. The handling advantages become clear in continuous-flow systems, where researchers need salts that withstand heating cycles and exposure to organic bases without rapid breakdown.

    Supporting Advanced Catalysis and Beyond

    The applications for this NHC precursor run broad and deep. In our earliest collaborations with research groups, we saw this compound unlock new possibilities in cross-coupling catalysis, carbon-nitrogen bond formation, and late-stage functionalization of pharmaceutical intermediates. By fine-tuning the sterics and electronics, this salt has consistently delivered on ligand performance for both homogeneous and heterogeneous catalyst systems. Several industrial labs rely on it to generate custom metals complexes with tailored reactivity. In gold catalysis, for example, our customers highlight the role of this NHC in promoting high selectivity and catalyst longevity.

    It doesn’t stop at catalysis. Over the years, some of our clients have integrated this product into the development of functional polymers, stable ionic liquids, and electrochemical devices. The high purity and batch-to-batch consistency we maintain are especially important when scaling from exploratory synthesis to pilot production. We worked closely with several research teams working in the field of materials science, where small amounts of impurities can impact the optical, thermal, or mechanical properties of end products.

    Specifications from Real-World Use

    From a practical point of view, chemists expect technical details they can rely on. Based on years of feedback and internal data, we supply 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride typically at a chemical purity exceeding 98 percent. Any remaining byproducts, such as unreacted starting materials or residual organic halides, fall below stringent analytical thresholds. After repeated conversations with practitioners, we decided to pack the product in nitrogen-purged bottles, reducing exposure to moisture and minimizing degradation between delivery and first use.

    After drying, our product demonstrates low water content, as measured by Karl Fischer titration, making it suitable for glovebox and Schlenk techniques. We monitor chloride content by argentometric titration, ensuring that the anion profile remains constant from batch to batch—something that plays a direct role in downstream NHC transfer and metal coordination steps. The powder form, developed after extensive screening, flows easily and resists caking, so it can be weighed and dissolved without static or clumping issues. This feature, seemingly minor, comes up often in customer feedback from both small-scale research and multi-gram catalyst synthesis.

    End-User Insights and Realistic Concerns

    Our work with synthetic chemists, process engineers, and analytical labs revealed how sensitive modern chemistry has become to even trace variations in materials. Early attempts to use alternative products from bulk suppliers often led to inconsistent results: sluggish carbene transfer, catalyst decomposition, color changes, and unexplained exotherms. Failures in chromatography or side-product formation have traced back to inconsistent purity or trace metals present in competitor products.

    Researchers fluorescence their own samples and find fewer contaminants in our product. College labs seeking to train students on cutting-edge synthetic techniques often request our lot documentation for classwork reproducibility. Some industrial partners, running larger scale productions, demand performance certificates and routine retesting as process conditions change, especially given the challenges of process validation in pharma or specialty chemicals.

    We continually track and respond to issues, both routine and unanticipated. Our QC staff scrutinize every analytical record, collaborating with clients on root-cause analysis when a batch behaves unexpectedly. We’ve supplied replacements after customers discover storage issues, and we have worked with major users to adapt our packaging to their atmospheric controls. In a few cases, we’ve collaborated in trouble-shooting when scale-up work revealed new impurity profiles previously unnoticed at lab scale. Our technical hotline and support network remain openly accessible to clients—not as a sales tool, but to ensure the material runs as intended in real world settings.

    Addressing Potential Challenges

    Any manufacturer dealing with sensitive organic and organometallic precursors must remain alert to shifting regulatory and environmental requirements. The raw materials behind this imidazolium chloride, most notably the specialized diisopropylphenyl intermediates, have fluctuated in availability and purity during the past decade. In the face of supply chain challenges—ranging from global transportation disruptions to sudden regulatory changes around solvent residues—we have built a backup network of vetted suppliers and tested procedures for rapid requalification.

    Customers sometimes ask if we offer alternatives with greener credentials. We continue to invest in research and development aimed at streamlining synthesis and reducing solvent waste. Internally, we recycle solvents and avoid hazardous purification steps where possible, passing on any cost efficiency directly to our user base.

    Concerns around chlorinated side products or trace metal impurities, voiced by environmental control and analytical safety departments, prompt us to run additional QC checks and publish impurity profiles for new lots. We have invested in ICP-MS and high-resolultion NMR equipment to raise detection sensitivity below legacy specifications, staying responsive to both evolving regulation and customer demand for deeper transparency. Each new batch heading to clients enters a review cycle so that we can quickly respond to reports of performance anomalies, even those first identified by a single end user.

    Looking Back: Evolution of the Product

    When we first introduced this imidazolium chloride, few in the wider industry appreciated how quickly demand would spread beyond academic research into industrial catalysis and process chemistry. We have since seen the compound find its way into semiconductor development, OLED material synthesis, and silicon wafer modification. Clients running continuous chemistry operations increasingly specify the need for robust, well-characterized NHC precursors, especially given the cost and time associated with downtime or off-spec batches in these high-value operations.

    The classic labeling—1,3-Bis(2,6-Diisopropylphenyl)imidazolium chloride—reveals only part of the story. Since the early days when researchers juggled different counterions, our customers have reported fewer difficulties with chloride as a counterion. In contrast to PF6 and BF4 salts, which sometimes hydrolyze or produce harmful byproducts under overly aggressive processing conditions, the chloride salt has proven adaptable in both academic and industrial scenarios.

    We keep close track of emerging research trends. The increased interest in photoredox catalysis, the use of flow reactors for continuous manufacturing, and the parallel development of “greener” transformations all push us to revisit both the product and process. Some clients require tighter specification for residual halides, others want packaging compatible with robotic dosing or high-throughput screening. Each new need becomes a driver for us to update our documentation, adapt packaging, or refine the purification sequence.

    Manufacturing Insights: The Human Element

    The story behind every batch we ship involves a blend of science, engineering, and good sense. Plant operators check reactor temperatures manually, not just by digital display, to catch subtle fluctuations missed by automation. Pedigree on starting materials matters; we track every drum and sample, sharing source and analysis so chemists on the receiving end know what’s in the bottle. Our quality systems rely as much on careful training and years of operator experience as on modern analytics. All this isn’t just practice—it’s lived necessity, proven every time a customer’s project depends on reliable chemistry in the flask.

    Sharing production experience with chemists who use our product allows us to find choke points in both supply chain and chemistry workflow that don’t show up in a typical spec sheet. When a batch requires custom drying or solvent exchanges to meet a particular application standard, our technical team coordinates with end users to meet those needs. We track process modifications and user feedback in our internal records, often adjusting parameters to support new chemistry developments across different industrial sectors.

    No matter how robust the process, unexpected issues still arise. We treat such events as opportunities to learn, not as failures to be concealed. A few years ago, a major research institution discovered a subtle impurity during scale-up for a novel polymerization project. Instead of shifting blame, our team ran additional analyses, confirmed the issue, and revised our purification method. The result generated not only a more reliable imidazolium chloride, but also a closer relationship with our clients built on transparency and shared goals.

    Paths Forward: Innovation Rooted in Day-to-Day Practice

    Working with this imidazolium salt, and supporting colleagues in dozens of research and production settings, has demonstrated how close the connection stands between R&D and manufacturing. Every improvement in purity or handling—whether it’s a change to crystal morphology or reduction in surface moisture—comes from hearing where users run into difficulty. Our R&D team partners with universities and industrial labs to test new forms, packaging, and trace impurity removal methods. Some recent pilot projects focus on adapting production to continuous reactors, offering rapid turnaround while preserving the same batch purity seen from traditional stirred batch reactors.

    We recognize that the expertise lies not only in running existing processes efficiently, but also in understanding where and how the field shifts next. Rising pressures for environmental stewardship and demand for more sustainable production fuels ongoing improvements. We consult with regulatory bodies, monitor global transportation changes, and adapt our logistics to accommodate shifting customs and handling rules—all to ensure uninterrupted and reliable delivery to our clients.

    Beyond simply shipping a bottle of 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride, our commitment is to be a partner in problem-solving. Open communication, batch traceability, and technical exchange remain the foundation—built one batch, one application, and one improvement at a time.

    Conclusion: A Product—and Partnership—Built from Experience

    Every gram we produce tells the story of chemistry, manufacturing, and hands-on collaboration. Through decades of direct engagement with both scientists at the bench and engineers on the plant floor, we have shaped 1,3-Bis(2,6-Diisopropylphenyl)Imidazolium Chloride into a product that delivers reliability and versatility with each batch. We look forward to supporting the next generation of discoveries that build on its foundation.