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1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid

    • Product Name 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid
    • Alias BTDA
    • 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

    856376

    Productname 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid
    Casnumber 92241-91-3
    Molecularformula C11H8N4O4
    Molecularweight 260.21 g/mol
    Appearance White to off-white solid
    Meltingpoint 238-242°C
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water, soluble in DMSO and DMF
    Smiles C1=CC=CC=C1CN2C=NN=C2(C(=O)O)C(=O)O
    Inchikey IJPHQSQCJWXESE-UHFFFAOYSA-N

    As an accredited 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid supplied in a sealed, labeled amber glass bottle with hazard markings.
    Shipping 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid is shipped in secure, sealed containers to protect against moisture and contamination. Packaging complies with chemical safety standards, and the product is clearly labeled with hazard and handling information. Shipping is typically conducted via ground or air freight, following all relevant regulatory and safety guidelines.
    Storage **Storage for 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid:** Store in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, well-ventilated area, preferably at 2–8°C (refrigerator). Avoid contact with strong acids and bases. Ensure proper labeling and secure storage to prevent unauthorized access or accidental spillage. Use suitable PPE during handling.
    Application of 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid

    Applications of 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid in Industrial Manufacturing

    1-Benzyl-1,2,3-triazole-4,5-dicarboxylic acid supports advanced material synthesis across several demanding industrial sectors, with each downstream segment requiring strict adherence to sector-specific safety and performance criteria. As the direct producer, we ensure every batch meets technical benchmarks for application in these specialized manufacturing environments.

    1. Corrosion Inhibitors for Water Treatment Systems

    This compound provides unique coordination properties for the formulation of multi-metal corrosion inhibitors, particularly in closed-loop water systems and high-pressure boilers, by forming film-forming complexes with metal surfaces to prevent oxidative damage, especially in aggressive aquatic conditions. Its functionality benefits equipment reliability and prolongs component lifespan, meeting demanding maintenance protocols.

    Industry compliance standards

    • ASTM D3477: Standard Practice for Testing Corrosion Inhibitors
    • ISO 8044:2015 (Corrosion of Metals and Alloys Terminology)
    • EU REACH Regulation (EC) 1907/2006, SVHC screening
    • Directive 98/83/EC—Quality of Water Intended for Human Consumption (for municipal applications)

    Typical usage ratio

    • Dosage typically ranges from 20 to 80 mg/L in circulating water systems, with the exact concentration based on system volume, metallurgy, and water chemistry variation.

    Downstream process integration

    • Integrate during the blending stage of corrosion inhibitor concentrate production. For industrial operators, dosing occurs in makeup water or directly into system recirculation lines prior to full-volume monitoring and adjustment.

    Final product types

    • High-performance multi-metal corrosion inhibitor concentrates
    • Boiler water treatment chemicals
    • Chilled water loop corrosion control blends
    • Municipal water distribution system supplements

    2. Chelating Agent for Electroplating Baths

    The material acts as a targeted chelant in electrodeposition baths for precious and base metals, controlling baths’ metal ion availability and reducing the risk of uneven plating due to unwanted precipitation. Its specific triazole structure helps minimize side reactions and DQ interruptions in copper, silver, and tin bath systems used in electronics and connector manufacturing.

    Industry compliance standards

    • ISO 4527:2014 (Electroplated coatings of nickel for engineering purposes)
    • IPC-4556 (Halogen-free Metallic Surface Finishes for Printed Boards)
    • RoHS Directive 2011/65/EU
    • Factory-specific wastewater pre-treatment and recovery guidelines

    Typical usage ratio

    • Bath component concentration is typically 0.1%–0.6% by weight of total bath solution, adjusted based on the target metal and end-use circuit board layer thickness.

    Downstream process integration

    • Add during bath make-up alongside supporting electrolyte salts and complexing agents; continuous monitoring ensures correct chelation stability throughout operating cycle.

    Final product types

    • Copper and tin electroplated circuit boards
    • Connector pins with enhanced adhesion layers
    • Leadframe packages in semiconductor packaging
    • Decorative and functional electroplated consumer connectors

    3. Building Block in Pharmaceutical Intermediate Synthesis

    This intermediate serves as a starting material for synthesizing heterocyclic compounds used in antimicrobial active pharmaceutical ingredients (APIs) and advanced research molecules. Its well-defined structure supports stepwise N-alkylation, acylation, and arylation routes for small-molecule drug discovery and pilot-scale cGMP manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals (US FDA)
    • European Pharmacopoeia (Ph. Eur.) Monographs (API level)
    • USP General Chapters for Sourcing and Traceability

    Typical usage ratio

    • Utilize as an equimolar reactant in condensation or coupling reactions, typically ranging from 10 g/L to 100 g/L depending on reaction scale; stoichiometry decided by the downstream intermediate pathway requirements.

    Downstream process integration

    • Employ directly in controlled synthetic steps, such as cycloaddition or amidation reactions, after standard solvent or solvent/water phase management and process filtration for impurity removal.

    Final product types

    • API intermediates for antifungal and antibacterial drugs
    • Laboratory reference standards and reference reagents
    • Batch-scale advanced intermediates for pilot trials
    • Regulatory filing support samples for small-molecule drug candidates

    4. Crosslinking Agent in Specialty Polymer Synthesis

    The compound functions as a bifunctional crosslinker in the preparation of triazole-modified polyimides and polyamide-based engineering plastics, imparting precise control over polymer architecture, enhanced resistance to chemical degradation, and improved mechanical resilience necessary for advanced electronics and automotive component applications.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems—Polymer Manufacturing)
    • ASTM D4066 (Standard Classification System for Nylon Polymers)
    • UL 94 (Flame Retardancy of Plastic Materials)
    • RoHS compliance for electronics-grade plastics

    Typical usage ratio

    • Crosslinker loading typically ranges from 0.5 mol% to 3 mol% relative to total monomer content; the selected level depends on desired molecular weight distribution and mechanical property targets.

    Downstream process integration

    • Add during polymer pre-polymerization or in-situ chain extension stage, ensuring homogeneous dispersion within the monomer matrix—use high-shear mixing to maximize crosslinking uniformity in the final resin blend prior to molding or extrusion.

    Final product types

    • High-performance polyimide films for electronics
    • Chemical-resistant polyamide components for automotive under-hood applications
    • Electrical insulation coatings
    • Membrane materials for fuel cell and lithium-ion battery separators

    5. Additive for Epoxy Resin Curing Systems

    Thanks to dual carboxylic acid functionality and aromatic triazole core, this compound enhances curing rate control and adhesive bond strength in advanced epoxy resin systems used for structural adhesives, coatings, and composite laminates in the aerospace and electronics sectors where both temperature performance and chemical durability are mandatory.

    Industry compliance standards

    • ASTM D1763 (Epoxy Resins Used in Electrical Insulation)
    • EN 45545-2: Railway Application - Fire Protection
    • IEC 61215 (Polymeric Materials in PV Applications)
    • REACH Annex XVII for restricted substances

    Typical usage ratio

    • Add at 0.2–2.0 phr (parts per hundred resin), value adjusted based on crosslink density and target glass transition temperature in the formulation process.

    Downstream process integration

    • Mix with base resin and curing agent during premix blending; monitor rheology and gel time at the compounding stage; post-cure at elevated temperature if required for final properties.

    Final product types

    • Epoxy structural adhesives for aerospace assembly
    • Electronic encapsulation compounds
    • High-strength protective coatings
    • Circuit board adhesive formulations
    Free Quote

    Competitive 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding and Leveraging 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid: Insights from the Manufacturer’s Bench

    What Sets This Triazole Derivative Apart

    Standing on the factory floor, it’s impossible to ignore the significance of niche heterocyclic carboxylic acids that chemists request, season after season. Among them, 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid (also known to many in the lab as BTDCA) often draws special attention. Developed within our reactors and handled by our process engineers since its earliest bench-scale synthesis, this compound delivers far more than just another node in the vast triazole framework.

    The backbone centres on the 1,2,3-triazole ring, renowned for its stability both thermally and chemically. The introduction of two carboxyl groups on the 4 and 5 positions sets this derivative apart from simpler triazoles. These carboxyl groups offer ready anchoring points for further transformation—an advantage our customers in advanced pharmaceutical and material science research pursue relentlessly.

    Adding a benzyl moiety at the N1 position isn’t for mere cosmetic effect. This structural tweak allows the molecule to gain bulk, improve solubility in certain organic media, and appear as a viable precursor in the preparation of more elaborate heterocycles. Our technicians routinely see requests for larger lots involving this motif, particularly as new click-chemistry routes gain ground across the fine chemical industry.

    Model and Specifications Tailored for Modern R&D

    Operating as a chemical manufacturer, every batch tells a story. We’ve developed our 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid from milligram-yield glassware runs to multi-kilogram reactors, responding to the evolving needs of both academic and commercial labs. Typical production follows a protocol that safeguards purity—usually not less than 98% HPLC, with residual solvents closely monitored by GC.

    Some research groups want it crystalline; others prefer amorphous solid. Most chemical reactions enjoy the fine, off-white to pale yellow powder that falls out of our final work-up and isolation stage. Melting point typically falls within the 210-215°C range; we monitor it batch by batch as another guardrail against decomposition and quality drift. Traces of benzyl chloride, azide intermediates, or toluene solvent are eliminated by systematic washing, careful pH modification, and filtration steps rather than relying solely on column chromatography—the sort of workshop detail that prevents headaches downstream in preparative and analytical processes.

    Keeping water content low (usually under 0.5% by Karl Fischer titration) extends shelf life and reduces risk of hydrolysis, especially when the product awaits further derivatization. Since carboxylic acids absorb moisture, humidity-controlled packaging isn’t an add-on; it’s a must. Secure bags sealed under nitrogen, with an outer drum for mechanical protection, arrive at our shipping dock ready for international dispatch.

    End Uses and Research Impact

    Researchers see beyond data sheets—every triazole stands for weeks of project work and mole calculations. Our BTDCA’s largest application lies at the crossroads of medicinal chemistry and advanced materials, where robust heterocycles serve as scaffolds for ligand design, crosslinking agents, or intermediates for more exotic target molecules.

    Colleague reports from university groups have confirmed that 1-benzyl versions of this dicarboxylic structure hold up well in Suzuki and Sonogashira cross-coupling. Many leading-edge drug-candidate synthesis programs now depend on the stability of both the triazole core and the carboxylic functionalities under these basic and transition metal-catalyzed conditions.

    Pharmaceutical development frequently demands dense functionality on small, stable cores. Here, this molecule offers what simpler triazoles can’t match: the convenience of two reactive carboxylic groups for peptide or amide linkage formation, tethered to a triazole that resists both oxidation and hydrolysis under normal operating conditions. As a result, project chemists press for reliability batch after batch, calling for uninterrupted supply, clear COAs, and traceability right back to source raw materials.

    Dental and polymer labs also report interest in using this dicarboxylic acid as a crosslinker or monomer feedstock, given the enduring interest in non-hydrolyzable, biocompatible linkages. The benzyl group confers just enough lipophilicity to modify the physical profile of resulting copolymers, expanding the toolbox for those developing new forms of dental resins or biomedical adhesives.

    Comparisons: Isomers and Analogues in Focus

    Plenty of labs start with simpler 1,2,3-triazoles—the unadorned ring or the 4-substituted versions. With BTDCA, the story grows more complex. Two carboxylic acids side by side on the triazole ring create more persistent hydrogen bonding, which changes solid-state behavior and improves control in crystallization or coordination experiments. These features matter in experiments that demand bulletproof purity, particularly in regulatory environments or scale-up work.

    Neighboring analogues such as mono-carboxy triazoles can’t offer dual-point conjugation, which limits their usefulness as linkers in bioconjugation routines or dendrimer formation. Further, alkyl-substituted triazole acids deliver different reactivity—and lack the aromatic stabilization of a benzyl group, which shifts spectral characteristics and sometimes complicates NMR assignments. Practicing chemists notice and act on such details.

    Procedure writers working in constrained pharmaceutical QA must account for every potential impurity. Products from traders or resellers sometimes show batches where color, odor, or purity slip out of spec; these weaknesses surface under UV, in TLC, or in attempted scale-ups. Our direct manufacturing control sidesteps those pitfalls, documenting stepwise oversight and client feedback in every process review.

    Manufacturing Lessons: From Reaction Kettle to Final Drum

    Making dicarboxylic triazole derivatives isn’t effortless. The stepwise process involves copper-catalyzed azide-alkyne cycloaddition (“click” chemistry), followed by careful protection and controlled hydrolysis. Those unfamiliar with azide chemistry often overlook hazards at scale—pressure buildup, exothermicity, and the potential for runaway reactions. We’ve spent years tuning reactor design, in-line monitoring, and batchwise additions to anticipate pressure or temperature excursions. Hazard management isn’t an afterthought; it flows directly from hands-on synthesis and accident review.

    Once the triazole ring closes, our work turns to carboxylation and purification. Crude reaction mixtures contain byproducts—such as polynuclear triazoles, copper salts, or unreacted starting azides—that must be stripped out decisively. As manufacturers, we never rely solely on theoretical yields or paper flowsheets. Only process validation by repeated small-to-medium scale trials tells the true story.

    Drying is a sticking point for carboxylic acid derivatives. Over-heating or prolonged vacuum sometimes leads to decarboxylation or discoloration. In response, our drying protocols lock in both safety and batch integrity, scheduling frequent sampling during solvent removal and adjusting ramp rates when necessary. Experience has taught us that process optimization doesn’t stop when a chemist leaves the bench; QA technicians and operators play critical daily roles in ensuring the final product matches the required fingerprint every time.

    Quality Assurance and the Value of Direct Traceability

    Customers tell us the worst surprises come not from chemical reactivity, but from inconsistent deliveries or opaque sourcing. For us, every drum carries an unbroken chain of records: raw material supplier, lot numbers, reaction dates, process adjustments, and QA checkpoints. This means our lab can address questions fast—a misplaced COA, a solubility anomaly, or an uncharacteristic melting range will trigger an in-depth review, not an email chain through intermediaries.

    Quality isn’t a buzzword here. Staff run regular batches through advanced HPLC, mass spectrometric verification, and impurity profiling, tracking degradation products even at levels below regulatory reporting thresholds. This vigilance empowers our clients to push boundaries with confidence—you wouldn’t believe how often a timely impurity report saves a customer months of wasted development time.

    We conduct stability studies in real time and at elevated temperatures, noting both short-term and long-term storage results. Lessons learned from these studies shape our advice to clients; we’ve guided several partners through successful upscaling by flagging reactivity trends invisible in two-week bench tests.

    Supporting Innovation and Facing Industry Pressures

    The surge in demand for complex triazole dicarboxylic acids reflects fast-moving trends in drug discovery, advanced coatings, and bio-conjugation technology. The only way to keep pace involves continual process development and technical exchange with researchers. Recent upticks in the use of 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid for modification of peptides and oligonucleotides illustrate this well. Direct amide formation from the free acid, under mild coupling conditions, allows researchers to access next-generation biologically active compounds without long protecting group strategies.

    Process scale-up teaches us about real-world industry pressures. While small lab syntheses might shrug off occasional erratic results, bulk operation on this product quickly exposes the shortcomings of vague procedures or poorly controlled work-ups. Our engineering staff monitor every column change, every shift from aqueous-organic partitions, and every deviation in mother liquor clarity. Only clear feedback loops between bench and manufacturing hall keeps our product development aligned with our clients’ goals.

    Our efforts to minimize residual metals, especially copper, arise from direct requests by pharmaceutical supply chains under tighter regulatory control. Chelating washes and ion-exchange treatments supplement our standard work-up, removing contamination down to the low ppm level. Only manufacturing experience in both small- and large-volume tanks has shown us what works—supplementing theory with direct sensory checks and analytics on each drum.

    Sustainability now leads most conversations on raw material selection and solvent choice. Solvent recovery rates, waste water treatment, and energy consumption all stand under daily review, leading us to trial greener alternatives where possible. It isn’t just compliance; resource conservation and community environmental impact hit closer to home as a manufacturer, not just a specification line item.

    A Closer Look at Research Collaboration

    Our engagement with R&D teams often starts with simple requests—different particle sizes, alternate salt forms, or routine analytical data. These exchanges build trust, then often deepen into collaborative method development. We’ve supported groups optimizing solid-phase peptide synthesis with BTDCA as a linker, sharing unique techniques to improve conjugation yield or minimize byproduct formation. This level of cooperation draws on our operational knowledge and fosters faster, more reliable R&D output.

    Supply chain reliability has also taken center stage for many international institutions—with import regulations tightening, origin certification and logistics support often rival the technical performance of the acid itself. Our documentation system, built from the ground up by production chemists and QA staff, supports rapid certification for customs, regulatory agencies, and research funding audits. There’s no shortcut; every kilogram reflects decades of process discipline.

    Feedback cycles rarely end after a single batch. Ongoing client reports fuel incremental improvement, whether in organoleptic properties, solubility management, or process scalability. Just last quarter, a partner reported an anomaly in UV absorbance for a new application. Our joint data review pinpointed a minor issue in recrystallization conditions, leading to an adjustment that pushed both our QC profile and their output higher. This kind of direct feedback sharpens our technical edge—and drives up quality for future projects.

    Navigating Regulatory Challenges and Ethical Considerations

    Serving pharmaceutical and biotech clients demands strict regulatory awareness. Direct traceability matters for cGMP, ISO, or other international frameworks. We’ve built rigorous site and document control protocols to meet annual audits from both third parties and our clients themselves. Beyond paperwork, this discipline encourages ethical sourcing—choosing sustainable raw material suppliers and following best practices for hazardous materials transportation and storage.

    Open reporting and accountability not only secure client confidence, but also form a sustainable business foundation. Ethical manufacturing, transparency in documentation, and adherence to EHS standards enable our team to produce at consistently high quality year after year, without the hidden costs or future liabilities some cut-corner operators suffer. Technical literacy and environmental stewardship walk hand in hand—every step in our process ties to operator safety, waste minimization, and responsible reporting.

    What the Future Holds for 1-Benzyl-1,2,3-Triazole-4,5-Dicarboxylic Acid

    As new research areas emerge, demand for multipurpose triazole dicarboxylic acids continues to expand. We see the next generation of peptide therapeutics, tailored nano-materials, and bioconjugates relying on rapid, reliable access to highly pure BTDCA. Our manufacturing scale and quality control answer this need with direct production oversight—bridging the gap between discovery and delivery.

    Ongoing R&D at our plant now explores more energy-efficient production routes and investigates alternate solvent systems with lower ecological impact. Early trials in continuous-flow chemistry offer encouraging signs, potentially unlocking greater consistency, scalability, and safety margins. Each process innovation stems directly from feedback at the bench, review in the pilot facility, and unyielding commitment to scientific rigor.

    The next chapters will no doubt bring new application notes, analytical techniques, and client-driven process adjustments. No automated system can match direct technician oversight, batch record transparency, and adaptability fostered by years of real-world practice. The culture of collaboration—both within our manufacturing group and with external scientists—keeps our process learning sharp and our quality visible on the frontlines of industrial and academic research.

    Any organization looking to unlock the value of specialty triazole carboxylic acids gains an edge with deliberate, granular process control and responsive cooperation. As a chemical manufacturer rooted in continuous improvement and scientific exchange, we’re committed to providing more than just product—we stand ready to help solve the challenges that new research and evolving regulations will bring.