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Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate

    • Product Name Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate
    • Alias CDTA
    • Einecs 205-900-3
    • 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

    773399

    Product Name Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate
    Synonym trans-CDTA monohydrate
    Chemical Formula C14H24N2O8·H2O
    Molecular Weight 372.36 g/mol
    Cas Number 94116-12-6
    Appearance white to off-white powder
    Solubility soluble in water
    Melting Point decomposes above 300°C
    Storage Temperature 2-8°C
    Purity typically ≥98%
    Ph approximately 2-3 (1% aqueous solution)
    Application chelating agent
    Density approx. 1.32 g/cm³
    Stability stable under normal storage conditions

    As an accredited Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic 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-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate, 25g, packaged in a sealed amber glass bottle with safety labeling.
    Shipping Shipping for Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate should occur in tightly sealed containers, protected from moisture and direct sunlight. The chemical is typically shipped at ambient temperature, classified as non-hazardous, but all relevant local, state, and international regulations for chemical transportation and labeling must be followed to ensure safety and compliance.
    Storage Store Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate in a tightly sealed container at room temperature, in a dry, well-ventilated area. Keep away from moisture, heat, and incompatible substances such as strong oxidizers. Protect from direct sunlight and ensure the storage area is labeled and accessible only to authorized personnel. Avoid generation of dust and wear suitable personal protective equipment during handling.
    Application of Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate

    Applications of Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate in Industrial Manufacturing

    Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate has become essential in sectors where advanced chelation, metal ion control, and stability are primary process requirements. The following sections detail real-world downstream applications focused on precision manufacturing and compliance-driven production environments.

    1. Pharmaceutical API Purification and Bulk Drug Production

    This raw material is utilized as a selective chelating agent during active pharmaceutical ingredient (API) purification to control trace metal contamination, thus ensuring stringent product quality for regulated drug synthesis. Pharmaceutical companies deploy this chelator especially in multi-step synthetic routes for peptides, antibiotics, and contrast agents where residual metal must remain below pharmacopoeia-mandated thresholds for patient safety and batch consistency.

    Industry compliance standards

    • United States Pharmacopeia (USP) residue on ignition limits
    • European Pharmacopoeia (Ph. Eur.) chapters 2.4.20 and 2.4.23 for metal catalysts/impurities
    • ICH Q3D Elemental Impurities Guidelines
    • cGMP (21 CFR Parts 210/211), with dedicated chelation specifications in batch documentation

    Typical usage ratio

    • Typically 0.01%–0.05% w/w by weight of crude API, adjusted according to measured metal ion residue and solubility profiles for target molecules

    Downstream process integration

    • Introduced post-reaction or during intermediate crystallization steps as an aqueous solution or blend, followed by controlled pH adjustment and filtration; employed prior to final milling, granulation, or lyophilization stages to ensure removal of metal traces

    Final product types

    • Bulk pharmaceutical ingredients (APIs)
    • Peptide therapeutics
    • Parenteral contrast agents
    • Finished dosage forms (tablet, injectable, lyophilized powder)

    2. Diagnostic Imaging Reagent Production

    Manufacturers of MRI and CT contrast media integrate this chelating agent as a core ligand during the synthesis of gadolinium or manganese complexes, ensuring high stability and safety in final contrast reagent formulations. The material’s strong affinity for lanthanide and transition metals supports compliance with strict product release specifications for human diagnostic use and shelf-life extension.

    Industry compliance standards

    • USP General Chapter <823> Radiopharmaceuticals for Positron Emission Tomography (PET)
    • European Pharmacopoeia monographs for gadolinium-based contrast agents
    • ISO 13485:2016 for medical device and diagnostic reagent manufacturing
    • FDA 21 CFR 610 (Biological Products: General)

    Typical usage ratio

    • Ligand-to-metal molar ratio typically 1.05:1 to 1.10:1, calculated based on batch stoichiometry and confirmed by analytical titration, with adjustments for process yield and purity control

    Downstream process integration

    • Directly charged as a ligand during metal complexation reactions under controlled pH and temperature conditions; followed by purification via chromatography or diafiltration and formulation into injectable grade solutions under aseptic processing

    Final product types

    • Gadolinium-based MRI contrast agents
    • Manganese-enhanced imaging reagents
    • Radiolabeled tracer molecules

    3. Water Treatment Additives in Semiconductor Wet Etching

    Producers of ultrapure water and etchant solutions for semiconductor fabrication utilize this chelating agent to prevent deposition of trace metallic contaminants on silicon wafers. This step is critical for advanced logic, memory, and optoelectronic device manufacturing, where yield and device reliability depend on sub-ppb metal ion levels in photoresist and cleaning processes.

    Industry compliance standards

    • SEMI F63/F57 (Semiconductor Equipment and Materials International standards for purity control)
    • ISO 9001:2015 with semiconductor-specific process validation
    • IEC 60747 (International Standard for semiconductor device manufacturing environments)
    • Customer-driven specifications for 99.9999% (6N) ultrapure process water quality

    Typical usage ratio

    • 0.5–3.0 ppm by total solution weight, depending on baseline ion content and targeted wafer geometries; periodically validated by ICP-MS trace analysis

    Downstream process integration

    • Dosed as a part of wet bench etching or post-etch cleaning formulations; introduced at the point of make-up tank blending and monitored in real-time using automated dosing and feedback from at-line purity meters

    Final product types

    • Semiconductor-grade wet etchants
    • Ultrapure cleaning solutions for wafer processing
    • Photoresist stripping chemicals

    4. Electroplating Bath Stabilization in Precision Metal Finishing

    In the formulation of high-performance electroplating baths for electronics and aerospace components, this chelating agent stabilizes transition metal ions, minimizes unwanted precipitation, and promotes uniform deposition throughout the plating cycle. Bath life extension and product surface finish directly depend on stringent metal ion management, particularly for microelectronics connectors and contacts.

    Industry compliance standards

    • IPC-4552 (Performance Specification for Electroless Nickel/Immersion Gold Plating)
    • ASTM B571 (Testing methods for metallic coatings adhesion)
    • RoHS Directive 2011/65/EU (restriction of hazardous substances in electrical/electronic equipment)
    • ISO/TS 16949:2009 for automotive and aerospace applications

    Typical usage ratio

    • 0.05%–0.15% v/v in bath composition, optimized through initial pilot runs and ongoing solution analysis, with adjustments for tank volume and residual metal concentration

    Downstream process integration

    • Incorporated during make-up of new bath or periodic maintenance additions; monitored via bath titration and process control logs to prevent metal hydroxide precipitation or substandard coating morphology

    Final product types

    • Gold, nickel, or copper electroplated electronic components
    • High-reliability PCB connectors
    • Precision metal housings for aerospace and instrumentation

    5. Industrial Cleaning and Metal Surface Preparation

    Industrial cleaning compound manufacturers apply this chelating agent to develop degreasers and metal preparation solutions for removing residual metal and oxide films from ferrous and nonferrous surfaces prior to painting or further chemical treatment. This ensures process baths maintain stable metal content and prevents fouling or pitting during downstream manufacturing, crucial for automotive, appliance, and heavy machinery sectors.

    Industry compliance standards

    • ASTM D4828 (Standard Test Methods for Practical Washability of Organic Coatings)
    • ISO 16232 (Cleanliness of components in hydraulic systems)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • OEM-specific specifications for paint adhesion and surface passivation

    Typical usage ratio

    • 0.1%–0.3% by total weight in alkaline cleaning formulations, depending on metal burden and bath turnover rates; adjusted via solution titration to maintain target performance

    Downstream process integration

    • Added to concentrated cleaner make-up; product is dosed into spray wash, dip tank, or ultrasonic cleaning lines before rinsing and subsequent conversion coating or painting applications

    Final product types

    • Industrial degreasing formulations
    • Pre-treatment solutions for automotive, appliance, and fabricated metal parts
    • Surface conditioners for subsequent electrocoating or powder coating
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    Certification & Compliance
    More Introduction

    Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate: Perspective from the Manufacturer

    A Closer Look at a Unique Chelating Agent

    Manufacturing chelating agents means more than just getting the ratios right in the reactor. Every batch forms the backbone for important progress in analytical chemistry, wastewater treatment, metal extraction, and even pharmaceuticals. Among these chelators, Trans-1,2-Diaminocyclohexane-N,N,N',N'-Tetraacetic Acid Monohydrate stands out — not only for its robust technical profile but also for the level of reliability and traceability demanded by scientists and engineers. Anyone who’s stood in a production hall understands that real quality emerges from a commitment to meticulous control, not simply from following a formula.

    Understanding the Molecule: Structure and Features

    Our production line for trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate (trans-DCTA·H2O) has evolved through decades of responding to research-driven requests and scale-up challenges. This compound features a cyclohexane scaffold locked rigidly in the trans configuration, flanked by tetraacetic acid functional groups. The firm structure lends a unique balance of hydrophilicity and rigidity, giving the molecule specific selectivity for metal ions that other chelators often miss. Where other agents such as EDTA or DTPA rely on linear or less constrained skeletons, the trans-1,2-diaminocyclohexane-based structure locks into complexes, shaping a distinct coordination geometry.

    We have spent years optimizing process variables — from the solubility of intermediate salts to pH adjustment protocols — so that the final product consistently offers a monohydrate content closely hugging its theoretical value. By maintaining that subtle water balance, the chelator performs predictably in both solution-phase applications and solid formulations. Moisture balance is nontrivial for those of us scaling from pilot to the metric-ton batches; it keeps shelf lives honest, batch-to-batch assay drift low, and instrument calibration reliable.

    Model and Specifications Shaped by Industry Demand

    Direct dialogue with our customers — lab leaders at universities, process engineers at electronic fabrication plants, regulatory chemists — has driven us to refine several models of this product. Most industrial and research users require material of high purity (typically ≥99%) with minimal trace metal contamination. By tweaking raw material sourcing and leaning on multi-step recrystallization, our core commercial grade reaches that purity benchmark. Particle size distribution comes into play in filter-based applications; our finer grades flow like powdered sugar, suitable for rapid dissolution. For scale-up processes, where clumping or dusting can waste both time and raw material, we’ve learned to calibrate bulk density within predictable ranges for reliable transfer and weighing.

    Some users focus on trace element analysis in environmental or food samples. For these folks, background contamination ruins whole runs of data. Our analytical reference grade undergoes additional purification steps, stripping background metals below 0.5 ppm. It’s a headache to keep tanks, wash water, and every valve ticking clean enough for this work, but there’s satisfaction in knowing that years of process upgrades translate into trust in your brand. Chemical manufacturing often sounds like a world of fixed recipes, but what keeps it alive is listening hard to what different end users actually measure and need.

    Usage in Analytical Chemistry and Beyond

    Ask any trace metals chemist: the accuracy of inductively coupled plasma (ICP) analysis starts with predictable chelation. Trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate forms stable complexes with ions such as calcium, magnesium, copper, nickel, and cobalt. In our own QC lab, we see how predictable those binding constants can be if synthesis is managed tightly. The rigid cyclohexane core limits distortion, leading to sharp endpoint titrations. This isn’t just a bench-top boast; it’s about clearing ambiguity from your calibration curves and reducing the need for re-runs.

    Besides analytical chemistry, the compound shows its worth in industrial water treatment, where users chase not only performance but also operational economy and environmental compliance. Traditional chelators sometimes leach too quickly, alter downstream pH, or prove tough to degrade. Trans-DCTA·H2O clings to metals more tightly in certain process conditions, particularly under elevated temperatures and broader pH swings, thanks to the ring rigidity and tetraacetic side arms anchored to the trans-diaminocyclohexane. That translates to better handling of complex wastewater streams and less risk of downstream precipitation.

    More advanced applications turn up in separation chemistry and materials science. Ion exchange columns packed with resin derivatized using this chelator can separate rare earth elements or heavy metals with selectivity not available from simple polyaminocarboxylates. And on the biological front, researchers build on this chelator’s selective coordination in MRI contrast agents, targeted metal-protein interaction studies, and even radiopharmaceuticals. Here, subtle differences in dummy atoms or hydration level shift kinetic properties in unpredictable ways. We’ve seen protein structural biologists request lot-specific certificates of analysis, all because the molecule's tiny variations tweak their final experimental outcome.

    Differences from Other Chelators: Experience from the Factory Floor

    Producing trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate lets us stand back and compare it directly with typical EDTA, EGTA, or DTPA. From a chemical standpoint, trans-DCTA presents a larger, more rigid chelating domain. That ring structure gives it sharper selectivity for ions that prefer defined octahedral geometry, allowing users to tease apart ions in mixed-metal environments. In large-scale extractions, that higher specificity minimizes the dragging in of unwanted ions, cutting down on extra purification steps — a direct production cost saver.

    We often field questions about why the monohydrate form matters. Run-of-the-mill EDTA often comes as a dihydrate or anhydrous variant. Those small hydration variations skew solution preparation, shelf stability, and even volumetric measurements for precision work. By sticking to the monohydrate, customers sidestep recalibration headaches and drift in sensory or analytical signals. Over the years, we have chased down every uptick in oven humidity, every glitch in drying cycles, because getting that final hydrate profile stable is what separates reliable lots from field failures.

    Operationally, trans-DCTA monohydrate attracts some users for its stability at higher temperature ranges and resistance to photodegradation, attributes linked to the cyclohexane backbone. If customers run continuous systems or batch reactions where room temperature can’t be guaranteed, those subtle differences can mean the difference between routine batch records and a series of process deviations. Put simply, the rigidity and layout of the trans-diaminocyclohexane frame changes what downstream chemical engineers can design — more than just a theoretical change on paper, this impacts waste streams, reaction windows, and final product validation.

    Challenges and Solutions in Large-Scale Synthesis

    Those who spend their days in chemical plants rather than in offices know that every multipurpose reactor brings quirks and surprises. Large-scale production of a specialized chelator like trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate runs into practical hurdles that rarely show up in patent outlines or journal articles. For instance, the condensation step between cyclohexanediamine and the acetic acid precursor generates a lot of exotherm, prone to runaway if your heat removal can’t keep up. In early years, we faced several batches going off spec simply because jacketed cooling struggled during seasonal temp shifts.

    After chasing the root cause, upgrading to a more responsive cooling circuit and installing multiple inline temperature probes finally dialed in batch consistency. Evaporation losses in monohydrate crystal formation forced us to develop a humidity-controlled drying room. Not every user cares about 0.05% differences in water content — but those shipping containers bound for pharma facilities do, and so does the documentation trail for regulatory audits.

    Cleaning validation takes on extra weight with this molecule, especially when the same line runs other amine- or carboxylate-containing products. A single misstep in tank flush or filter cake disposal can spike metal backgrounds or contaminate product. Dedicated equipment sections, segregated pipelines, and rigorous post-run chelation flushes solved the majority of these risks. Investments in high-purity water systems and trace analysis built a production environment where QA teams spend their time on real process improvements, not crisis response.

    Regulatory and Quality Demands: Transparency Earns Trust

    From a manufacturer's perspective, quality isn’t only about numbers on a certificate of analysis. Incoming audits come from customer technical teams and from regulatory bodies. Heavy metal contents, trace impurities, and even microbiological levels — all details matter more in this product because end-users implement it in sensitive analytical, environmental, and sometimes pharmaceutical processes. Over time, this pressure reshapes SOPs, documentation processes, and the employee training cycle.

    As more regions implement ever-stricter environmental and product purity standards, we have found it necessary to invest in enhanced in-line monitoring and laboratory analytics. Running old-school batch tests does not cut it when users expect digital lot traceability. Linking our process analytics with end-to-end documentation secures the chain of custody and helps guarantee the stated purity. We’ve learned that changes as modest as a shift in supplier for a minor reagent can nudge heavy metal contamination — so every lot of every raw material now draws a full trace metal analysis before release to production.

    Transparency with our partners pays dividends. When customers raise questions about water content, possible background ion presence, or even the particle size profile, being able to respond quickly — pulling analysis records or trend data from our lab LIMS — locks in trusting relationships. Competition in chelating agents is not about the lowest price per kilo but about providing a solid technical foundation for end users who cannot risk failures in their processes. Just as problems in our plant can appear unexpectedly, so can issues in a customer’s bench work; our job is to supply stability amid that unpredictability.

    Looking Forward: Innovations and Emerging Uses

    A manufacturer’s experience often means bridging the present and the future. Our development staff have worked directly with academic groups pushing new uses for trans-1,2-diaminocyclohexane-derived chelators — from supporting catalysts in asymmetric synthesis, to novel extraction of critical rare earth elements from spent electronic devices. These projects start in grams but sometimes quickly leap to pilot kilograms. Scaling new synthesis or purification schemes rarely goes according to plan. Starting points from lab notebooks often forget that heat transfer, crystallization rates, and filtration scale non-linearly; it takes feedback from actual production halls to iterate quickly and avoid costly dead ends.

    In recent years, demand from medical imaging and diagnostic labs has driven a search for purer, more consistent batches, especially with isotopic labelling or custom metal loading. Only a line experienced in running GMP-compliant intermediates can convincingly guarantee traceability from flask to final shipment. We take pride in pushing our older equipment to achieve those levels, retrofitting continuous monitoring and documentation. For customers working in first-in-human trials or submitting data to regulatory agencies, that level of detail transforms a simple bottle of chelator into a linchpin for new diagnostics.

    Sustainability considerations now drive the design of our future lines, both from practical necessity and regulatory direction. Spent mother liquors from chelator synthesis can pack metal ion loads too high for standard discharge; we run secondary cleanup reactions and capture waste streams for recycling. Pressure from customers to deliver documentation about carbon footprint, lifecycle analysis, or green chemistry benchmarks has picked up, pushing our team to document exactly where inputs and process efficiencies improve overall impact. This goes way beyond plant compliance and reaches as far as our suppliers, trucks, and storage facilities — a complete ecosystem viewed through a more transparent, measurable lens.

    Why Technical Dialogue Really Matters

    One thing becomes clear after years at the plant: customers who can talk real-world problems help us manufacture better products. Some reach out with unexpected trace signals in their chromatography, others with fouling issues in industrial water systems, and a few with poor chelation efficiency due to competing ions. Seeing these issues through the eyes of customers gives us targets for what to measure, what to improve in production, and how to deliver a product that truly adds value rather than just ticking a box.

    Listening to the stories from project leads, analysts, and site engineers tells us far more than raw sales data. If a batch doesn’t perform as expected, investigating back through process notes, batch records, and analytical logs brings opportunities for continuous improvement. That feedback has directly inspired upgrades in how we manage raw material storage, redesign packing and drying stages, and respond to special sample requests.

    Improving Outcomes, Batch after Batch

    The typical user of trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate demands an assurance: will this lot keep their data pure, their processes on schedule, and their outcomes reproducible? This demand shapes how we design every step of production, check every shipment, and collect every data point. Reliability emerges not from a single clever process tweak, but from constant investment in quality control, raw material vetting, equipment calibration, and open lines of communication — both inside the plant and with every customer who knocks on our door.

    Looking back, the culture of manufacturing — daily attention to detail, respect for process, willingness to adapt — transforms a specialized molecule into a foundation for countless technical applications. For us, each bottle or drum of trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate leaving the warehouse represents years of incremental technical progress, continuous dialogue, and shared trust between producer and end user. The path forward will no doubt demand even tighter standards and more transparent data, but these are demands we welcome. Every batch stands as testament to what is possible when manufacturing and science move forward together.