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trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate

    • Product Name trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate
    • Alias CyDTA Monohydrate
    • Einecs 239-241-5
    • Mininmum Order 1 g
    • Factory Site West Ujimqin Banner, Xilingol League, Inner Mongolia, China
    • Price Inquiry sales7@bouling-chem.com
    • Manufacturer Bouling Chemical Co., Limited
    • CONTACT NOW
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    Specifications

    HS Code

    315596

    Product Name trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate
    Chemical Formula C14H22N2O9
    Cas Number 24716-19-0
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point Decomposes above 260°C
    Purity Typically ≥98%
    Storage Temperature Room temperature
    Ph Range Solution 2.0 - 3.0 (in water)
    Synonyms CDTA, trans-1,2-Diaminocyclohexanetetraacetic acid
    Hydration State Monohydrate
    Uses Chelating agent

    As an accredited trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate, 25g, supplied in a sealed, labeled amber glass bottle with tamper-evident cap.
    Shipping Trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate (from Sigma Aldrich/Merck/TCI, chemical grade) is shipped in securely sealed containers to prevent moisture ingress. It is packaged according to standard chemical safety protocols, including labeling and documentation. Shipping complies with local and international regulations to ensure safe handling and delivery of this laboratory reagent.
    Storage Store trans-1,2-Cyclohexanediaminetetraacetic acid monohydrate (Sigma Aldrich/Merck/TCI chemical grade) in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from moisture, heat, and direct sunlight. Avoid storing with incompatible substances such as strong oxidizers or acids. Keep the storage area clearly labeled and follow the safety and handling guidelines provided in the material safety data sheet (MSDS).
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    Certification & Compliance
    More Introduction

    trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate: A Chemist’s Perspective

    Shaping Solutions with trans-1,2-CDTA·H2O

    For many years working in the synthesis and manufacturing of specialty chelating agents, few products match the versatility and performance of trans-1,2-Cyclohexanediaminetetraacetic Acid Monohydrate, better known among formulation chemists as trans-1,2-CDTA·H2O. Our direct experience takes us well beyond the catalog description, into the real impact this compound has had across analytical chemistry, water treatment, and metal separation projects.

    Understanding Its Structure and Model

    trans-1,2-CDTA·H2O brings together the hexadentate binding capability of EDTA, with a rigid cyclohexane backbone that sets it apart from the more flexible ligands in the market. Its full name describes the core: a trans arrangement of amino groups on the cyclohexane ring, each bearing tetraacetic acid arms, balanced by one molecule of water as monohydrate. This rigidity increases selectivity in chelation reactions, helping chemists target specific metal ions with much greater control compared to traditional aminopolycarboxylates. We produce the trans isomer for its reliable performance, ensuring batch-to-batch consistency in purity and hydrate levels to match demanding research and industrial standards.

    Specification and Quality Consistency

    Our development process began with trial synthesis in small reactors. Gradually, we engineered scalable methods, optimizing crystallization to guarantee the monohydrate form, which assures solubility and reaction predictability. Every lot undergoes checks for moisture content, heavy metal impurities, and particle size, using methods we validated through comparison testing. For methods like potentiometric titration or inductively coupled plasma spectrometry, unwanted metal contaminants compromise results, so we go the extra mile with purification steps to keep concentrations far below detection thresholds. Chemists rarely see this side of the work, but it makes a measurable difference across many applications.

    Chemical Properties that Drive Demand

    People often ask what makes trans-1,2-CDTA·H2O so favored by analytical laboratories, especially when EDTA or DTPA appear to offer similar functionality. It really comes down to geometry. The constrained six-membered ring in cyclohexane forces the attached nitrogen atoms into positions that enhance binding affinity for certain metals, such as calcium, manganese, and rare earth elements. This translates into strong, selective complexes—more so than with the more flexible ethylenediamine core of EDTA. The water solubility, especially in its monohydrate form, saves time in solution preparation and minimizes undissolved residues, supporting smoother workflows for those working with metal analysis or biochemical applications.

    Real-World Advantages Over Other Chelating Agents

    Working alongside our industrial partners, we’ve put trans-1,2-CDTA·H2O in direct competition with other agents. In metallurgical pilot projects, its resistance to hydrolysis under high pH conditions ensured metal extraction remained effective even under harsh process cycles. In complexometric titrations, analysts appreciated its sharper titration endpoints, particularly with alkaline earth and transition metals. Academic customers exploring environmental remediation have leveraged its higher chelation stability to capture and remove heavy metals from test streams, an outcome that lesser agents struggled to match.

    Some ask why not just scale up the use of EDTA. Over time, we learned that small differences in structure lead to meaningful performance changes. For example, in the presence of iron(III), EDTA often forms less stable complexes, while the cyclohexane ring in trans-1,2-CDTA·H2O resists breakdown, sustaining the chelation process for longer. Where higher selectivity for a target ion matters—such as isolating lanthanides or actinides—this alternative agent repeatedly delivers better separation indices.

    Challenges in Synthesis and Scale-Up

    No innovation comes easy. Early attempts to synthesize trans-1,2-CDTA on pilot scale turned up unexpected byproducts, particularly cis isomers and overalkylated variants. Even small amounts of these alter the chelating profile, so purification steps became vital. Through redesigning the reaction sequence and using specialized crystallization equipment, we succeeded in producing the nearly pure trans isomer. Controlling water content, rinse cycles, and drying conditions ensured a stable monohydrate. These efforts translated into a product that users could rely upon, without concerns over variability or off-specification batches.

    Much of the work focused on minimizing energy and solvent use, both from a cost and environmental perspective. Moving from batchwise to continuous crystallization, we cut waste by over a third. We’ve since incorporated real-time monitoring for pH and temperature, fine tuning the process to achieve the monohydrate with hardly any lost product. This direct experience gave us insights not just into better chemistry, but into sustainable scale-up.

    Matching to Applications: End-User Results

    Researchers investigating trace metal content—especially in environmental samples—found that trans-1,2-CDTA·H2O delivered accurate results in scenarios where other agents gave ambiguous curves or variable recoveries. In many soil and water analysis protocols, the product’s tighter complexes resisted interference from competing matrix ions. Where EDTA sometimes fell short, with fractionated extraction stages and poor reproducibility, trans-1,2-CDTA·H2O consistently outperformed it. Chromatography labs integrating it into their sample prep saw fewer anomalies, especially in the extraction and quantification of specialized rare earth elements and transition metals.

    In the realm of catalysis, complexation with transition metals and subsequent ligand exchange reactions often run more smoothly using trans-1,2-CDTA·H2O. The thermodynamic stability of its complexes makes it an attractive choice for kinetic studies, where product isolation and catalyst recovery rely on the robustness of chelation. One collaboration with a major catalytic process developer revealed that this compound withstood repeated cycles of acid/base treatment, holding on to its target metal ions through a dozen washes. This resilience cut material losses noticeably, backed by detailed recovery and process efficiency data.

    Beyond the Laboratory: Environmental and Industrial Perspectives

    In wastewater treatment, selective complexation can either simplify or complicate downstream processing. Chelators with poor selectivity or instability release metals prematurely, making capture inefficient and increasing regulatory risks. Our product’s stronger complexes reduce the risk of metal breakthrough. Effluent monitoring records showed that using trans-1,2-CDTA·H2O lowered residual heavy metal concentrations, even when processing feeds with fluctuating composition.

    Plant operators commented on the benefit of lower dosing levels, a direct result of higher affinity constants. Instead of constant adjustments to compensate for chelator degradation, they found that once their process stabilized, the system needed less oversight. Fewer chemical additions lowered material costs and maintenance requirements. In applications targeting high-value recycle streams—such as nickel or cobalt recovery from batteries—these features translate to improved economics.

    Some sectors, especially in electronics and plating, turned to trans-1,2-CDTA·H2O to maintain product integrity and prevent unwanted deposition. Trials in copper and tin plating baths demonstrated lower contamination and smoother, brighter finished surfaces. In these sensitive processes, even minor deviations in chelating agent quality can cause visible product defects. By prioritizing strict production parameters and in-house analytics, we provide a reliability advantage not easily replicated by less rigorous producers.

    Differentiating Through Chemistry and Practice

    Our day-to-day experience showed the importance of hands-on practice in distinguishing between products with similar descriptions. The “trans” configuration doesn’t just represent a structural curiosity—it influences every aspect of the molecule’s behavior, from how it wraps around a target ion to how it resists thermal and chemical breakdown. Unlike ethylenediaminetetraacetic acid or NTA, the cyclohexane core applies mechanical strength to the molecular scaffold. This matters when dealing with complex matrices, such as contaminated groundwater or high-residue process circuits.

    Competitor products, often made in bulk without attention to isomer purity or moisture control, rarely achieve the same level of consistency. Once, during a supply shortage, we evaluated several imported alternatives. Our laboratory found variances in solubility, unidentified side products, and erratic titration performance. The differences have nothing to do with the specifications sheet; they show themselves only under working conditions. In our view, chemical manufacturing means more than just producing compounds—it compels a commitment to end-to-end stewardship, from raw material sourcing through final packing.

    Quality Through Direct Control

    Choosing not to delegate production or outsource quality assurance, we keep everything on site, using our own reactors and testing facilities. Teams monitor each stage, reviewing crystal morphology, batch data, and impurity profiles. Lessons from failure are as valuable as those from success; every missed purity target results in a process review and adjustment. We spend time talking with end-users to learn exactly what matters in their context—be it solubility at low temperature or trace metal background in high-sensitivity analysis. This feedback loop refines our process and keeps us ahead of industry shifts.

    For long-term storage, we recommend keeping product in tightly sealed containers away from direct humidity sources. While the monohydrate form is less prone to caking than anhydrous variants, moisture uptake changes the apparent mass and can subtly alter reaction concentrations. In scaling for bulk delivery, we adjusted our packing process to eliminate excess void space and use moisture barriers, ensuring customers receive the product as intended, ready for use without adjustment.

    Supporting Advancements in Research

    Trans-1,2-CDTA·H2O plays a role in helping researchers tackle modern problems, especially as studies require higher precision and reproducibility. In geochemical speciation work, isolating rare elements from complex matrices hinges on reliable chelation, a fact confirmed by peer-reviewed publications citing our material’s superior recovery rates. In medical diagnostics, fine-tuning metal ion extraction leads to improved assay accuracy, crucial for both patient outcomes and regulatory compliance.

    Looking back, the journey to producing a high-quality chelating agent involved not just following established procedures, but responding actively to changing market needs. Regulations on heavy metal discharge, stricter analytical controls, and specialized customer requirements shaped every upgrade in our facility and quality protocol. As scientific understanding of coordination chemistry progressed, we adapted methods, invested in tighter analytical controls, and brought in new talent who saw the potential in rigid-structured agents like ours.

    Potential and Responsibility Moving Forward

    Emerging applications create new possibilities for trans-1,2-CDTA·H2O. In battery recycling and critical mineral extraction, engineers seek agents that selectively bind metals even in harsh chemical environments. Our work with national laboratories and technology developers revealed that as material flows become more complex—with multiple competing contaminants—the margin for subpar chelation tightens. Success depends both on molecular design and on reliable, transparent production. We invite collaboration and open discussion about specific challenges; in-house chemists can adapt batch parameters, test custom purity runs, or troubleshoot performance anomalies.

    The greatest lesson remains that product quality comes from a chain of individual actions, not from a single written specification. Fielding calls from customers working late nights or solving unexpected process bottlenecks goes hand in hand with batch recordkeeping and method improvement. Whether supplying gram-scale lots for research or tonne loads for process chemistry, the aim stays the same: make sure that the product performs as expected, supports customer innovation, and stands up to independent scrutiny.

    Practical Solutions for Ongoing Challenges

    From a producer’s vantage, supply continuity and technical support present the largest ongoing opportunities for improvement. Global logistics disruptions occasionally introduce risk to raw material sourcing. To counter this, we keep inventory of critical reagents and maintain relationships with alternative suppliers. On-site storage and redundant analytical instruments help buffer the impact of such events. Recurring education—both internally and for our customers—proves essential. Sharing handling tips or solution preparation guidance saves labs hours of troubleshooting and reduces waste.

    Efforts continue to minimize waste streams and improve process sustainability. Realizing that chemical manufacturing involves environmental footprint as much as technical achievement, we invest in solvent recovery, energy efficiency upgrades, and safe waste handling. The academic and industrial partners we work with increasingly value documentation around emissions, lifecycle impact, and safe product stewardship. This reflects a collective move towards responsible innovation, not just in the utility of the compound, but its broader role in a sustainable manufacturing ecosystem.

    Long-Term Value from Deep Chemical Knowledge

    Trans-1,2-CDTA·H2O serves as a clear example of how fundamental chemistry, combined with rigorous production and ongoing customer collaboration, yields solutions that meet both routine and advanced needs. By taking ownership of both chemical structure and production process, we not only provide a better product, we offer a resource for tackling complex technical challenges. Over the years, our team built a practical foundation in cyclohexane-based ligands. By applying this depth of expertise, we support both today’s demanding applications and the frontiers of what chelating agents can achieve.

    Every shipment tells the story of careful synthesis, conscious scale-up, and commitment to delivering a reliable tool for chemists, engineers, and researchers. The difference shows itself not only in specification tables, but in smoother lab routines, reproducible data, and successful scale-ups. Direct feedback keeps us on target, ensuring that the practical value of trans-1,2-CDTA·H2O emerges fully in the hands of those who need it most.