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HS Code |
269269 |
| Product Name | 1H-1,2,3-Benzotriazole-5-Carboxylic Acid |
| Chemical Formula | C7H5N3O2 |
| Molecular Weight | 163.13 g/mol |
| Cas Number | 1670-14-0 |
| Appearance | White to off-white powder |
| Melting Point | ≥ 240 °C (decomposes) |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥ 98% |
| Storage Temperature | 2-8 °C |
| Synonyms | 5-Carboxybenzotriazole |
| Structure Type | Aromatic heterocycle |
| Ec Number | 216-785-6 |
| Smiles | C1=CC2=NC=NN2C=C1C(=O)O |
As an accredited 1H-1,2,3-Benzotriazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 50-gram amber glass bottle, tightly sealed, labeled “1H-1,2,3-Benzotriazole-5-Carboxylic Acid,” includes hazard and handling information. |
| Shipping | **1H-1,2,3-Benzotriazole-5-Carboxylic Acid** is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically handled as a non-hazardous, stable organic compound, but appropriate safety labeling and documentation are included. The package complies with standard chemical shipping regulations to ensure safe and secure delivery. |
| Storage | 1H-1,2,3-Benzotriazole-5-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Avoid exposure to moisture and direct sunlight. Store at room temperature and ensure containers are clearly labeled. Use appropriate personal protective equipment when handling to prevent contact with skin and eyes. |
Applications of 1H-1,2,3-Benzotriazole-5-Carboxylic Acid in Industrial ManufacturingAs a direct producer of 1H-1,2,3-Benzotriazole-5-Carboxylic Acid, we supply this raw material for advanced, specification-driven sectors where chemical purity, traceability, and consistent process performance are critical. Below, we detail major application scenarios, highlighting regulatory requirements, formulation ratios, integration steps, and realizable end products. 1. Corrosion Inhibition for Industrial Cooling Water SystemsDownstream formulators use 1H-1,2,3-Benzotriazole-5-Carboxylic Acid as a selective corrosion inhibitor, particularly for copper and its alloys in recirculating cooling water. The material offers controlled protection under variable pH and high-chloride environments, enabling operators to extend system uptime and maintain heat exchange efficiency without major disruptions for cleaning or maintenance. Its carboxylic group provides superior metal surface adhesion, delivering targeted performance for open and closed-loop industrial systems. Industry compliance standards
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2. Electroplating Chemical AdditivesSpecialists in metal finishing incorporate this compound as a grain-refining and leveling agent for copper, nickel, and silver electroplating baths. The molecule modulates electrode surface kinetics by adsorbing at the metal-ion interface, enabling finer deposit morphology, reduced pin-holing, and shinier, more mechanically robust plated layers. It is particularly suited for printed circuit board (PCB) and precision connector fabrication, where deposit uniformity and microstructural consistency are non-negotiable. Industry compliance standards
Typical usage ratio
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3. Synthesis of Photostabilizers for Polymer ManufacturingOur compound serves as a key intermediate in the synthesis of benzotriazole-derived UV stabilizers used in engineering plastics and specialty films. By incorporating the molecule, downstream producers access enhanced light absorption and radical scavenging, protecting finished polymers from ultraviolet-induced color change, mechanical degradation, and loss of gloss. These photostabilizer systems often target polycarbonate, PA, and ABS resins used in high-spec construction and automotive parts. Industry compliance standards
Typical usage ratio
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4. Laboratory Reagent in Analytical ChemistryThe compound finds application as a high-purity analytical reagent for trace metal detection and chemical research. Its chelating properties and stable carboxylic structure enable precise calibration standards in ion chromatography, complexometric titration, and research on corrosion mechanisms. Universities and certified commercial laboratories rely on its batch-certified purity for accurate, interference-free measurements in published studies and notified testing protocols. Industry compliance standards
Typical usage ratio
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Chemists rarely ask for 1H-1,2,3-benzotriazole-5-carboxylic acid unless their project has reached a point where basic intermediates just can’t fill the gap anymore. At our facility, every batch of this compound starts with high-purity starting materials and tight process controls. We trust our team’s daily vigilance and a belief that a molecule only becomes truly useful when its purity stands up to tough analytical scrutiny. We look at each lot under HPLC, make sure the melting point lands squarely on the reported range, and check residual solvents are measured in the low ppm. Typical specifications see purity above 99% by HPLC, and by the time it moves out the door, our people have checked color, pH in solution, and insoluble matter. No batch leaves our plant unless QC can match each result with standard samples from certified lots. Each time, the lab staff talks us through the chromatograms to settle any ambiguity, since the presence of closely related triazole impurities can complicate downstream synthesis or formulation.
This compound sits squarely in the benzotriazole family. It carries a carboxylic acid group at the 5-position, offering a distinct synthetic handle that sets it apart from parent benzotriazole. As a direct manufacturer, we see the most common usage in medicinal chemistry, specifically during SAR campaigns, as well as in building reference standards and specialty ligands for coordination chemistry. Some researchers make use of the acid group for esterification or amidation, expanding the compound into new chemical space. In corrosion inhibition, the carboxyl function opens new possibilities for tailoring surface adhesion, a requirement in electronics manufacturing and aerospace surface treatment where baseline benzotriazole doesn’t always anchor tightly enough.
There’s a temptation in specialty manufacturing to talk mostly about numbers and purity, but the real difference often comes down to what happens during scale-up. Early stages favored small glassware, but as projects moved beyond hundreds of grams, we committed to dedicated glass-lined reactors. This avoids metal ion contamination, especially important since this compound can complex with transition metals and skew downstream analytical work. After crystallization, we rely on vacuum filtration, continual solvent recycling, and air-dry rooms filtered for particulate count, because even minor dust or solvent residues can create headaches in pharmaceuticals.
Some customers work with kilogram quantities, asking for the fine powder form to simplify solution preparation. Others prefer coarse granules to minimize dust, especially those who automate handling. We’ve listened to both sets and adjusted our drying and milling steps accordingly. Particle size is routinely checked by laser light scattering, not just sieving, because reliable performance in automated synthesizers calls for reproducibility at this level. There are stricter standards in research labs using robotics, so we separate lots by granulation and maintain records going back several years, ensuring a chain of custody and traceability with each shipment.
Many chemical companies, whether trading or distributing, view benzotriazole analogs as undifferentiated listings on a catalog page. We’ve learned that researchers, especially those in fragment-based drug discovery, value the unique reactivity of the 5-carboxylic acid moiety. Unlike the unsubstituted backbone, 1H-1,2,3-benzotriazole-5-carboxylic acid lets chemists anchor the molecule through a carboxyl group, broadening the types of linkages or surface attachments they can explore. Various bioconjugation protocols depend on stable, regioselective functionalization, and routine benzotriazole often can’t accomplish this without extra metal catalysts or activation steps.
Several pharmaceutical clients use this compound to build PROTAC linkers or peptidomimetics, ways of targeting proteins that demand both chemical resilience and selective binding. The positional substitution pattern offered by the 5-carboxyl variant enables a richer functional landscape, and that’s something off-the-shelf chemicals just can’t replace. Diagnostic chemists appreciate the carboxylic acid’s ability to form strong non-covalent interactions with protein residues, which becomes essential during structure-based assay development.
In the corrosion inhibition field, which includes aerospace component production and semiconductor etching, the performance edge comes from covalent anchoring: the carboxy group bonds tenaciously to oxide-rich surfaces. Simple benzotriazole can’t deliver this, so the additional acid opens new applications in anti-tarnish coatings where standard products can falter, particularly under thermal cycling or humid conditions.
Between our team and the end user, a lot can happen. Oxidation and light exposure pose risks, so we pack every order in cold-sealed, opaque containers and use argon backfilling for large-scale shipments. Each lot includes a measured water content, typically under 0.5%, so hygroscopicity won’t complicate formulation. Most standard benzotriazoles, especially technical grade, risk higher levels of moisture, which can degrade over time or during repeated bottle opening. We learned the hard way—years ago a poorly sealed drum led to clumping and an angry customer rerunning a week of synthetic work.
Beyond shipping, many customers want insight into shelf stability. We run real-time and accelerated aging studies. Real lots, real fridges, no simulated data. Most samples show less than 1% decomposition after one year at 25°C, with no significant change in melting point or UV-Vis absorbance profile. This means less waste and less reordering for our clients in academic, pharmaceutical, and manufacturing settings. Brands focused on distribution often blend and re-pack product, but our direct chain from production to storage means every user gets what our analytical lab signed off on, no dilution, no question about date of manufacture.
A direct comparison between this compound and 1H-benzotriazole itself doesn’t capture the most important metric: reactivity. The 5-carboxyl group unlocks transformations simply not possible with unmodified benzotriazole. Practically, this means researchers can synthesize amides, esters, and N-linked conjugates without long detours or harsh conditions. For instance, standard carboxyl-activation chemistries, such as EDC/NHS or CDI, work smoothly on our 5-carboxylic acid intermediate, providing access to peptide conjugates or surface ligands. These processes routinely fail or require harsh conditions with simple benzotriazole.
From experience, we know that 1H-1,2,3-benzotriazole-5-sulfonic acid, often chosen for water solubility or detergent applications, caters to a different set of customers. The sulfonic acid group helps with dispersion in aqueous environments, but doesn’t offer the same reactivity for coupling chemistry, especially where selectivity or minimal background hydrolysis is critical. We keep both materials on hand, and see requests for our carboxylic acid more frequently from those working on antibody-drug conjugates or diagnostic chip surfaces.
The 4-carboxylic acid isomer exists, but synthesis routes tend to give impure mixtures, as para-substitution encounters competing ring activation. In contrast, our method for the 5-carboxylic acid streamlines purification and keeps costs lower. Pharmaceuticals and polymer chemists view this difference as more than academic; every impurity—or even positional isomer—can derail downstream reactions or regulatory approval. Feedback from development chemists at leading pharma companies shaped our purification protocols, and we’ve never had to recall or replace a lot due to positional isomerization.
Chemical production always carries environmental responsibility. Within our plant, all solvent waste channels through a dedicated cleaning and distillation system, which has reduced total solvent discharge by more than 60% in ten years. Benzotriazole-based compounds sometimes trigger regulatory review due to aquatic toxicity. We’ve tested our waste streams, and by maintaining tight segregation of process-affected water, we keep effluent loads below the local reporting threshold. This extra step means higher costs but less headache, and in states with stricter regulation, customers don’t call us about supply chain interruptions or product embargoes.
Every drum shipped carries batch-level trace data. This includes analytical reports but also certifications showing compliance with European and US REACH guidelines. Our chemistries rely on reliable, ethically sourced raw materials. As the original manufacturer, we hold the chain of custody from kilogram lots of starting triazole through to the final acid product, so customers can audit not only quality but also ethical and environmental sourcing.
The practical reality is that while distributors juggle supply from multiple origins, we actually witness every stage from reactor charge to final packaging. This puts our technical staff in a position to answer real questions about sustainability and long-term compliance. When the community turned renewed attention to PFAS and similar persistent chemicals, our early transition to greener solvents helped keep us ahead of regulatory trends.
1H-1,2,3-benzotriazole-5-carboxylic acid doesn’t sell itself as a commodity, and we haven’t built our business around marketing one-size-fits-all solutions. Instead, project chemists and process developers have consulted us about tweaking scale, morphology, or even salt formation where process optimizations could unlock downstream value. During collaborations with universities and early-stage biotech firms, our chemists provided in-process samples, helped investigate reaction bottlenecks, and supported on-site troubleshooting. This engagement fostered partnerships that go beyond transactional sales and helps everyone, ourselves included, learn more about the essential role of this building block in innovation.
Working with academic labs exploring new proteolysis-targeting chimeras, we have adjusted process protocols to produce slightly modified versions with custom isotopic labeling or increased batch-to-batch consistency suitable for biological assays. In these situations, upstream transparency makes all the difference. Our technical staff documents all changes and provides annotated synthetic pathways when customers request it, and this consistency allows for clear structure-activity relationship development in research.
We participate in industry consortia that encourage sharing of best practices around benzotriazole derivatives, since innovation often follows open communication—not closed catalogs or undisclosed provenance. By staying rooted in actual production and technical support, we find that these conversations help shape not just the chemistry, but also standards and approaches to new regulatory challenges.
As a direct producer, we prepare product documentation including Certificates of Analysis, validated analytical data, and compliance statements according to customer regulatory needs. Pharmaceutical companies, in particular, request complete documentation for every lot. Our on-site storage gives us full access to batch archives, so revisiting any sample for retesting poses no problems if any concern arises downstream with a customer.
Data integrity and electronic batch records protect both our clients and us. Each lot carries associated spectra, method details, and dates to support regulatory filings, or in some cases Pre-IND applications. Unlike brokers or resellers, our connection to each phase of manufacture gives peace of mind: customers get consistent lots, know exactly what goes into their processes, and have a direct line back to the people behind the chemistry. This level of assurance is something only achieved by those with boots on the ground at the production site—not a third-party warehouse.
Consistent, defendable analytical verification is sometimes what makes or breaks a pharmaceutical candidate as it moves into regulatory assessment. Our technical and QC teams reconcile every discrepancy, whether it comes from new user methods or changes in internal protocols.
The development and application landscape for 1H-1,2,3-benzotriazole-5-carboxylic acid continues to evolve. New drug modalities, advanced diagnostics, and precision hardware demand functional molecules that do more than sit in storage. We’re seeing growing demand from fields like bioconjugate chemistry, polymer modification, and electronics fabrication. All of these developments hinge on the chemical leverage that the 5-carboxy group delivers, especially in coupling and surface binding applications.
Partnerships with innovators keep us connected to the needs of cutting-edge research. Our technical team makes adjustments based on real research feedback, because single-use applications — or entirely new industries — push us to revisit every assumption about scale, purity, and packaging. We work closely with clients looking for specialty formats or advanced intermediates not found in standard catalogs. These challenges drive our process team to consider not just cost or speed, but deeper questions of stability, reactivity, and implementation in the real world.
Real experience and honest feedback from the production floor to the customer lab form the backbone of what we offer. Staying involved in direct manufacturing connects us to shifts in regulation, new scientific breakthroughs, and the practical challenges facing modern chemistry. That’s the real story behind every shipment of 1H-1,2,3-benzotriazole-5-carboxylic acid we send out: a blend of exacting process, daily technical dialogue, and a commitment to advancing the work of those who depend on us.