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2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate

    • Product Name 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate
    • Alias CDMT
    • Einecs 629-418-2
    • 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

    546563

    Cas Number 60044-21-5
    Molecular Formula C5H11BClF4N2
    Molecular Weight 222.41 g/mol
    Appearance White to off-white solid
    Melting Point 82-86 °C
    Solubility Soluble in acetonitrile, dichloromethane
    Boiling Point Decomposes before boiling
    Storage Temperature 2-8 °C
    Purity Typically ≥98%
    Synonyms CDI·HCl·HBF4, Chlorodimethylimidazolidinium tetrafluoroborate
    Chemical Structure Imidazolidinium ring with two methyl and one chloro substituent, paired with tetrafluoroborate anion
    Hazard Statements Causes skin and eye irritation

    As an accredited 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with tamper-evident cap, white hazard-labeled exterior, 25g net weight, securely sealed for chemical safety and storage.
    Shipping 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate should be shipped in tightly sealed, chemically resistant containers. Protect from moisture and direct sunlight. Store and transport under cool, dry conditions, following all relevant chemical safety regulations. Handle as a potentially hazardous material. Shipping may be subject to local, national, and international regulations relating to hazardous chemicals.
    Storage 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from strong bases, acids, and incompatible substances. Ensure the storage area is equipped with secondary containment and clearly labeled. Avoid exposure to heat or direct sunlight and minimize contact with skin or eyes.
    Application of 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate

    Applications of 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate in Industrial Manufacturing

    As the direct manufacturer, we provide 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate for a select group of downstream industries that demand high-purity, stable, and effective chlorinating or activating agents in their core production processes. Below, we detail concrete industrial scenes where our chemical serves irreplaceable roles, citing specific regulatory frameworks, usage guidelines, key processing stages, and final product lines established by global market leaders.

    1. Pharmaceutical API Production—Peptide Synthesis

    In peptide manufacturing, our compound functions as an efficient coupling and activation reagent, facilitating peptide bond formation with improved selectivity and minimized side-product formation. Contract manufacturing organizations (CMOs) and API producers integrate this raw material during both solid-phase and solution-phase peptide synthesis, addressing the rising complexity in drug-targeted peptide therapeutics.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) monographs on peptide APIs
    • U.S. Pharmacopoeia (USP) procedures for peptide synthesis
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.5 equivalents per carboxyl group in peptide sequences, adjusted for peptide chain length and steric hindrance

    Downstream process integration

    • Charge to reactor following N-protected amino acid addition for in situ activation on resin or in solution
    • Used in conjunction with base and solvent (commonly DMF or NMP) under inert atmosphere
    • Quenching and resin washing precede cleavage and deprotection steps

    Final product types

    • Custom therapeutic peptides (injectable, oral, or topical forms)
    • Generic peptide APIs for diabetes, oncology, and metabolic indications
    • Diagnostic peptides used in immunoassay kits

    2. Agrochemical Active Ingredient Synthesis

    This specialty reagent acts as a chlorinating or activator component in the downstream synthesis of select agrochemical actives such as fungicides and plant growth regulators, where controlled chlorination and minimized byproduct are critical for regulatory compliance and product efficacy. Crop protection manufacturers value its selectivity in heterocyclic intermediate steps.

    Industry compliance standards

    • EPA FIFRA Registration (USA) for new active substances
    • ECHA REACH compliance (EU) for manufacturing and importation
    • ISO 9001:2015 for bulk agrochemical production
    • China National Standard GB 20665 for pesticide intermediates

    Typical usage ratio

    • 0.6–1.2 molar equivalents, adjusted per target substrate and desired yield

    Downstream process integration

    • Introduced at mid-stage synthesis during heterocycle functional group installation or activation
    • Reacts at controlled temperatures (15–30°C)
    • Followed by aqueous or solvent-based work-up and downstream purification (e.g., crystallization or solvent extraction)

    Final product types

    • Active ingredient concentrates for broad-spectrum fungicides
    • Azole or imidazole-based growth regulators
    • Pre-formulated oil or water dispersible agrochemical preparations

    3. Advanced Material Synthesis—Ionic Liquid and Electrolyte Development

    Manufacturers of battery and advanced material components use our raw material to synthesize ionic liquids and high-performance electrolytes, where its reactivity and compatibility with tetrafluoroborate systems provide desirable conductivity and stability. Electrochemical device suppliers value these electrolytes in lithium batteries and supercapacitors for increased safety margins and thermal resistance.

    Industry compliance standards

    • IEC 62660-2:2018 for battery safety testing
    • UN/DOT 38.3 for transport of lithium cells and batteries
    • ISO 9001:2015 for specialty chemical intermediates
    • RoHS Directive (EU 2011/65/EU) for low-halogen, low-metal content

    Typical usage ratio

    • 0.9–1.3 molar equivalents per precursor, tailored to anion–cation pairing of final ionic liquids

    Downstream process integration

    • Introduced in controlled environment reactors with dry, inert atmosphere
    • Reaction proceeds at low-to-moderate temperatures (5–40°C) to form quaternary ammonium salt electrolytes
    • Followed by vacuum or solvent-driven purification and drying

    Final product types

    • Ionic liquids for electrochemical analysis and synthesis
    • High-purity electrolyte salts for lithium-ion batteries
    • Conductive media for supercapacitors and advanced capacitor films

    4. Fine Chemical Synthesis—Heterocyclic Intermediate Manufacture

    Producers of fine chemicals employ our product as a selective chlorinating agent or coupling promoter to construct N-heterocyclic intermediates for pharmaceutical, agrochemical, or specialty pigment production lines. Its specificity enhances yield and purity in steps where off-pathway reaction minimization directly impacts final compound integrity.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production process control
    • OECD Good Laboratory Practice (GLP) for intermediate development
    • ECHA REACH registration dossier requirements (for handled volumes)
    • National/local hazardous chemical management rules (e.g., China’s Catalog of Hazardous Chemicals)

    Typical usage ratio

    • 1.0–1.4 equivalents per target substrate, customized following initial process validation and impurity profile analysis

    Downstream process integration

    • Added to stirred batch reactors post-charging of base heterocycle and co-solvent (DMF or DCM typical)
    • Real-time monitoring with HPLC or GC until endpoint achieved
    • Quenching and extractive work-up to yield isolated intermediate

    Final product types

    • N-heterocyclic building blocks for advanced pharmaceutical intermediates
    • Pigment precursor molecules (e.g., for specialty organic dyes)
    • Agrochemical intermediate scaffolds (non-commodity, high value-added lines)
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate: A Closer Look from the Manufacturing Floor

    Our Experience with 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate

    Operating in chemical manufacturing, we often get requests for reliable and scalable sources of 2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate—frequently abbreviated by research groups as CDI-TFB or CDMTB. This compound draws attention for its stable handling and its utility in a range of organic transformations. Through direct production and repeated client interaction, we have observed a set of consistent demands that have shaped our own QC workflows and specification design. Unlike upstream intermediates, this salt bridges fine chemical synthesis with more complex industrial production. Our batches reflect process discipline—consistent color, precise particle sizing, and clear batch traceability. Surprises in reactivity or purity can slow down a downstream synthesis or spoil an R&D project, so practical reliability remains our highest production aim.

    From Process Batch to Laboratory Bench

    Manufacturing begins with careful attention to the raw materials. Impurities slip downstream and create byproducts or performance outliers. We rely on direct sourcing of amines and chlorinating agents, always verifying that each meets tight GC and LC standards before moving them into the reaction vessel. Our controlled chlorination and subsequent ion-exchange keep side products at bay. Since water content directly impacts salt performance and flowability, each drying step occurs under vacuum with careful temperature monitoring. Finished CDMTB passes Karl Fischer titration and multi-point NMR scrutiny before packaging. We mark every bottle with a unique batch code, so researchers can trace back any issue to a discrete production run.

    Clients expect a white, free-flowing solid—not a sticky powder, not a lumpy mass loaded with residual solvent. We package material only after verifying flowability and passing sieve certification. This hands-on touch avoids loss of yield in the customer’s operations. The benefit shows up immediately: less time spent grinding or transferring powders in glassware, more focus on maximizing their own synthesis outcomes. Customers—academic and industrial alike—often remark that our lots dissolve quickly and handle with ease, reducing contamination risk and clean-up effort.

    Why Purity and Particle Size Make a Difference

    Our chemists approach CDMTB synthesis with a working knowledge of the key reactions that end users pursue. Whether preparing peptide bond formations, activating carboxylic acids, or improving the selectivity of nucleophilic coupling strategies, CDMTB must avoid unpredictable reactions. One impurity can introduce trace byproducts at the scale of milligrams—an annoyance for analytics, a stopper for pharma-grade work. Through regular performance testing, we have found that even seemingly minor deviations in chloride or BF4 content affect yield and reaction rate, especially for moisture-sensitive reactions.

    CDMTB’s main appeal lies in its near-anhydrous state and quick dissolution. Tight control over moisture (<0.2%) came only after months perfecting our vacuum-dry protocols and testing multiple carriers for safe transfer. Particle size also came under scrutiny, not as a cosmetic issue, but because clumplike grains take longer to dissolve and can lag in in situ activation steps. Our experience led us to screen by mesh size, preferring a medium powder form that avoids both dusting and agglomeration. Both purifiers and blenders in our workflow check against published standards but add our in-house controls as insurance.

    Distinguishing CDMTB from Other Activating Agents

    Comparisons often come up between our CDMTB and traditional activating agents like carbodiimides, uronium or phosphonium salts, and imidazolium-based alternatives. Each material brings strengths and quirks. Carbodiimides such as DCC or EDC have dominated amide coupling, but create urea byproducts that must be filtered away. Phosphonium reagents perform efficiently, yet they sometimes require careful handling and post-reaction purification. Uronium salts excel in certain peptide syntheses but introduce extra cationic residues. Imidazolium salts closely related to CDMTB offer high reactivity yet bring lingering impurities that complicate post-reaction clean-up.

    Our own tests—with direct feedback from partnering synthesis labs—demonstrate CDMTB’s advantages in dryness, cleanup, and predictable shelf stability. Its tetrafluoroborate anion offers inertness toward nucleophiles and acids, which allows for wide compatibility with both acid- and base-sensitive reactants. Compared to carbodiimide-based agents, CDMTB produces cleaner filtrates, a key reason why medicinal and process chemists turn to us for repeat supply. Its handling profile also makes it a better choice where chloride or TFA residues can disrupt downstream analytics or stability.

    Application Experience: Successes and Challenges

    On the practical side, researchers use CDMTB in the activation of carboxylic acids for amide and ester formation. The mechanism to form reactive intermediates appears straightforward, yet the purity of the raw coupling agent changes reproducibility. We’ve discussed organic synthesis with several R&D and pilot teams—the material needs to respond to small tweaks in base, solvent, and temperature, and must not introduce surprises through hygroscopicity or lingering side-products. Some customers pursue peptide couplings under mild conditions, exploiting the salt’s high solubility and minimized byproduct profile. Others put it into materials science, using it to mediate surface modifications of polymers, where even trace impurities hinder functional performance. In both cases, feedback guides slight tweaks in our batch process—sometimes adjusting crystallization temperature, sometimes retuning the sequence of washes.

    We recognize challenges as well. CDMTB, though less hazardous than many halogenated organics, asks for steady handling to avoid dust exposure and hydrolysis—the same properties that support high reactivity also create a need for good PPE and drybox work in scale-up environments. As a manufacturer, we respond by offering detailed handling tips drawn from our own experience, not just relying on the SDS: use tightly sealed dispensers, limit open times, clean bench spills immediately, and reject off-color or off-odor product. These suggestions come from folk who have handled thousands of kilos and seen what repeated exposure can bring in real working conditions.

    Specifications, Stability, and What Matters to Chemists

    We repeatedly hear requests from researchers: offer true, analytically supported specs, not just the bare legal minimum. That’s where our in-house analytics shine, providing full NMR, IR, and elemental analysis tabulated on a per-batch basis. The moisture content and chloride ion levels tell trained eyes a lot about what the material will do in their reaction set-up. Shelf stability also trumps theoretical numbers; we routinely test stored samples from previous production runs in simulated humid environments to verify that no decomposition occurs. Our monitored storage conditions mirror those in the field—cool, dry rooms or nitrogen-flushed cabinets—so reported results stay relevant to real-world application.

    Customers often compare different brands, noting differences in bulk density and pack-out which affect lab transfer and massing accuracy. Too dense, and the powder fails to flow; too loose, and it drifts or cakes on the scale. We fine-tune our granulation and anti-static packaging with these issues in mind, adjusting only as user feedback justifies change. In multi-kilo or multi-gram format, we supply both the bulk industry and the boutique lab, conscious that handling needs diverge between a 10-tonne tote and a research-size jar.

    Each new application offers a learning curve. Our relationships with university research groups, contract manufacturers, and global pharma innovators deepen our insight into the edge cases where CDMTB stands out—or falls short. Our scale-up notes and troubleshooting records remain open to regular revision. The most reliable lessons arise from hands-on experience: which solvent mixtures drag in water, which base/acid ratios boost coupling, and how each tweak impacts final product purity or filterability. Our support desk draws on the cumulative experience of our technical team, not boilerplate responses.

    Environmental and Regulatory Aspects

    A responsible manufacturer pays attention to the environmental profile of any produced chemical salt. While CDMTB does not carry the volatility or acute toxicity of many halogenated reagents, disposal and flushing controls matter. We design production runs to minimize mother liquor waste. Most spent streams undergo treatment through pH adjustment and salt concentration reduction. Where solvents such as acetonitrile or dichloromethane must be used in synthesis or purification, closed-loop systems capture, refine, and redistill where feasible. These choices lower both emissions and downstream compliance cost, with added benefit to workplace safety.

    Many regulatory agencies ask for proof of absence of certain residuals—chlorinated or fluorinated byproducts in particular. Our facility meets GMP-comparable standards based on regular third-party audits. Each certificate reflects direct testing, not just supplier guarantees. We work closely with logistics partners to ensure safe, legal delivery to a broad range of regulated markets.

    For export, we track requirements country-by-country, as customs rules for specialty chemical salts are constantly evolving. Our staff seeks ongoing regulatory education to stay ahead of new requirements and prevent shipment delays on the customer’s end. Whenever possible, clients receive supporting test results—often including extra analyses outside standard requests—for risk-free qualification, especially for scale-up or production validation.

    Supporting Responsible Use—Lessons Learned from the Shop Floor

    Providing CDMTB does not stop at sale; our team fields technical questions and offers direct feedback from our process chemists to users facing application or scale-up challenges. Our technical team assembles periodic best practices guides based on collective experience. Typical advice concerns storage—keep the lid tight, store over desiccant, inspect regularly for signs of moisture. Reactivity guides draw from pilot-plant runs, noting which side-reactions have cropped up at excess concentration, and what solvent swaps avoid them.

    We learn, too, from customer feedback: which residues occasionally slip by when working outside the ideal pH range, the filter media that prevent fines loss, or tips for combining CDMTB with green solvents without loss of performance. Sometimes, research teams uncover oddities—rare impurities not picked up in routine screening, or unexpected shelf-exposure effects. Each report feeds into a continuous improvement loop, from lab to production to QC.

    Custom Formats and Batch Adjustments

    Industrial chemistry requires flexibility—a lesson we’ve absorbed over hundreds of batches. While basic CDMTB shipments remain our core, we respond to specific requests: alternate mesh sizes for automated powder handling, modified drying cycles for low-static fill, or extra aliquoting to prevent moisture uptake during repeated use. Clients developing medical or electronics-grade products sometimes ask for extra documentation or on-the-fly purity enhancements. Our team handles custom fill orders with hands-on verification, not just automated packaging. Each request finds its way to our formulation chemists, where process notes fine-tune delivery without disrupting routine QC.

    Some downstream users need blends or pre-mixed streams using CDMTB as the key activator. We control blending tanks to minimize cross-contamination, and validate blends through full spectral analysis. The practice remains rare, since most researchers value pure, unblended salt. But as new domains emerge—particularly in specialty polymer modification or surface functionalization—we expect more requests for tailored pre-mixes. Our flexible production line adapts, so development cycles shrink and new chemistries reach product teams more quickly.

    Comparing CDMTB—Feedback from Real End Users

    Chemists often share their verdict after using freshly sourced CDMTB side by side with alternate activators. The most cited advantages involve handling: no irritating vapor, few to no dust-control issues at the bench, and rarely any cross-redox concerns with secondary reagents. Labs scaling up from bench to pilot find that our lots match or outperform on repeatability, which stems from consistent control of both input materials and process steps. A common frustration with other activating agents lies in unexplained batch-to-batch fluctuation—assay numbers that never quite add up, or nuisance solubility mishaps that waste days in rework. Our internal QC logbooks chart two decades of gradual tuning, so we’ve eliminated most recurring pain points.

    Some clients, particularly contract developers and process chemists, point out the practical gains in waste management. CDMTB’s tetrafluoroborate salt byproduct leaves filtration residues that are easier to separate and neutralize than those from phosphorus- or chlorine-rich reagents. That translates to smaller environmental burden and lower after-use disposal costs. Feedback cycles between pilot and process batches find that reliability makes the biggest impact—not just clean papers, but smooth transfer to production scale where regulatory scrutiny rises.

    Innovations and the Future of Specialty Reagents

    Growing demand for selective, efficient chemical transformations keeps us focused on innovation. Our team continually tracks academic literature and patent filings for improvements in activating salt synthesis. Small changes—smarter crystallization, improved solvent recovery, better atom economy—offer both cost and technical performance benefits. We recently initiated collaborations with university research groups to probe greener synthesis pathways, aiming to minimize halogen source dependency and shrink waste streams. Progress comes in steps: refining a stepwise protocol here, adjusting a drying sequence there—each tweak contributes more reliable salt to the marketplace.

    Interest grows not only in traditional amide and ester coupling, but in new domains: advanced materials, specialty pharmaceuticals, and analytical sample preparation. As these fields evolve, CDMTB features in more application notes and cross-disciplinary collaborations. Each represents an opportunity to learn from real-world application challenges, update manufacturing playbooks, and share findings with a wider network of practitioners.

    Our Commitment to Quality and Trust

    As direct manufacturers, we see every step from raw material testing to final packaging. Our plant engineers and lab technicians confront practical realities on each shift: a slightly off-color batch, a subtle drift in particle sizing, or a rare oversight in solvent exchange. We trace each to root cause and work out a fix before batches ever reach the client. No marketing claim replaces lived experience—mistakes leave traces, though years of attention clear most away long before products ship out the warehouse door. Our staff stands behind each container, knowing that trust is earned in grams and kilos, not just in certificates and glossy sales sheets.

    Long-term clients count on our input for project planning, troubleshooting, and regulatory adaptation. Their successes and challenges shape the evolution of our operations. We share these improvements as openly as regulatory protections and nondisclosures allow, confident that better understanding drives safer and more effective chemistry around the globe. Our open-door policy welcomes tours, audits, and hands-on QC reviews at any time of year. Proof lies on the shop floor, not just in spreadsheets or slides.

    The Road Ahead

    2-Chloro-1,3-Dimethylimidazolidinium Tetrafluoroborate continues to attract wider attention for good reason: stability, selectivity, and straightforward waste profile. From a manufacturer’s perspective, the real challenge is simple—deliver consistent, high-performing salt at all scales, and offer honest feedback. Ongoing dialogue—whether sparked by a new synthetic challenge or a process bottleneck—keeps improvement steady. Success emerges from decades of hands-on production and a few lessons hard-earned. The research and industrial chemistry communities can depend on CDMTB and its direct producers as partners in innovation, with every batch telling a story of careful development, practical insight, and direct accountability.