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HS Code |
705115 |
| Cas Number | 615-14-7 |
| Molecular Formula | C7H6N2O |
| Molecular Weight | 134.14 g/mol |
| Iupac Name | 2-hydroxy-1H-benzimidazole |
| Appearance | White to off-white crystalline powder |
| Melting Point | 300-302 °C (decomposes) |
| Solubility In Water | Slightly soluble |
| Smiles | Oc1nc2ccccc2[nH]1 |
| Pka | 11.5 (approximate, for the NH group) |
| Synonyms | 2-Hydroxy-1H-benzimidazole; Benzimidazol-2-ol |
As an accredited 2-Hydroxybenzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Hydroxybenzimidazole is packaged in a 100g amber glass bottle, clearly labeled with hazard warnings, product details, and batch number. |
| Shipping | 2-Hydroxybenzimidazole is shipped in tightly sealed containers to prevent moisture and contamination. Packages are labeled according to chemical safety regulations and transported under cool, dry conditions. Ensure compliance with local and international shipping guidelines for handling non-hazardous laboratory chemicals. Handle with appropriate personal protective equipment during loading and unloading. |
| Storage | 2-Hydroxybenzimidazole should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep in a cool, dry, and well-ventilated area, separated from incompatible substances such as strong oxidizers. Proper labeling and secure shelving are essential. Personal protective equipment should be used when handling to prevent skin and eye contact. Follow all institutional safety and chemical storage protocols. |
Applications of 2-Hydroxybenzimidazole in Industrial ManufacturingAs a direct manufacturer of 2-Hydroxybenzimidazole, we serve a range of specialized industrial sectors where this intermediate contributes to product stability, process efficiency, and regulated performance. Below, we outline major downstream contexts in which our material plays a practical and standards-driven role, with clear data on formulation and processing requirements. 1. Corrosion Inhibitors for Water Treatment2-Hydroxybenzimidazole is widely applied as an organic corrosion inhibitor in closed and open-loop water treatment systems, effectively reducing metal oxidation in industrial chillers, heat exchangers, and water pipelines, particularly where systems operate under alkaline or neutral pH. Users integrate it with other chelants and dispersants for enhanced system protection, considering local discharge limitations and specific metallurgy. This additive is a trusted choice in the automotive, HVAC, power plant, and petrochemical engineering sectors to extend equipment life under demanding operational cycles. Industry compliance standards
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2. Accelerator in Rubber VulcanizationThis chemical acts as a secondary accelerator in the vulcanization of natural and synthetic rubber, especially in the production of specialized industrial elastomers. It is utilized for its ability to fine-tune cure kinetics and crosslink density, which influences final product resilience and service temperature. Vulcanizer manufacturers leverage its performance where standard thiazole accelerators require enhancement, providing control over cure rates and minimizing reversion under prolonged heat exposure, critical for heavy-duty belts and seals. Industry compliance standards
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3. Intermediate for Pharmaceutical SynthesisThis compound plays an essential role as an intermediate in the synthesis of cationic dyes and select licensed APIs, including benzimidazole antifungals and proton pump inhibitor scaffolds. Its use in pharma manufacturing prioritizes high purity and accurate stoichiometry. The product supports regulatory compliance through traceability and process validation, and manufacturers deploy it in cGMP-controlled reaction pathways, focusing on synthesis yield and impurity control for active drug substances and excipient bases. Industry compliance standards
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4. Ligand for Metal Complex CatalystsHigh chemical stability and chelating ability make this compound an effective ligand for preparing transition metal complexes, notably for homogeneous catalysis in fine chemicals and polymer manufacturing. Its deployment in catalyst synthesis requires strict control of impurity levels and moisture content to maximize catalytic activity and reproducibility, vital for continuous and batch catalyst applications in the synthesis of specialty chemical building blocks and monomers. Routine analysis ensures compliance with catalyst efficiency benchmarks and safety criteria for chemical handling. Industry compliance standards
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5. Stabilizer in Colorant and Dye FormulationsThe antioxidant and UV-stabilizing properties of this compound are critical in improving the shelf life and photostability of cationic dyes and inkjet colorants. Textile dye and ink manufacturers employ it to mitigate fading and oxidative degradation during storage and usage, ensuring color-fastness under extended sunlight exposure. Its role as a stabilizer is especially prevalent in applications where finished goods undergo stringent weathering tests and high-speed application processes, such as in digital textile printing or packaging materials. Industry compliance standards
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Operating a chemical manufacturing facility puts the value of experience on display every day. A product like 2-Hydroxybenzimidazole (2-HBI) doesn’t just come off the line by accident. There are years of incremental improvements in synthesis, real-world feedback from researchers and downstream users, and a constant drive to reduce impurities batch to batch. Our approach focuses on thoroughness: careful sourcing of raw materials, meticulous temperature control during cyclization steps, and unwavering diligence for moisture management during drying and storage.
2-Hydroxybenzimidazole carries the CAS number 615-16-7 and presents as an off-white to pale-yellow crystalline powder. With the molecular formula C7H6N2O and a molecular weight of 134.14 g/mol, its structure—a fused bicyclic ring with a hydroxy group at the second position—tells you a lot about what it can do. Purity matters. In our operations, every kilogram is tested by HPLC for assay confirmation above 99%, monitored for trace metallic contamination, and screened for consistent melting point (283-287°C) because we’ve learned that even a one-degree deviation signals the need to trace and correct upstream process variables.
Chemistry shouldn’t exist in a vacuum. Most applications of 2-Hydroxybenzimidazole start in the research lab but move rapidly to industrial-scale uses. Our customers span pharmaceutical R&D organizations pursuing benzimidazole-based drug candidates, pigment and dye formulators, and polymer companies searching for high-performance building blocks. The hydroxy group on this molecule allows for custom substitutions, targeted etherification, and complex protection/deprotection strategies—a versatility that pure benzimidazole simply cannot offer.
Medicinal chemistry often drives demand. We see formulation scientists using 2-Hydroxybenzimidazole as a key precursor for antifungal and anti-ulcer drug preparation. They count on chemical consistency because minor impurities at this node can propagate through multi-step synthesis, compromising not just yield but also patient safety in the final API. This responsibility isn’t theoretical: Every batch destined for pharmaceutical use passes through a QA review backed by traceable batch records and retained samples.
Manufacturers of advanced pigments and resins lean on 2-Hydroxybenzimidazole for its ability to generate colorfast, high-durability compounds. In polymer development, its bifunctional nature (aromatic ring and hydroxy group) introduces sites for hydrogen bonding and cross-linking that boost mechanical and thermal performance. This is not academic speculation; our partners in the coatings industry report measurable gains in abrasion resistance and shelf life against more conventional aromatic amines.
We regularly get asked: Why not use benzimidazole itself, or other hydroxy-substituted heterocycles? The answer reflects direct experience in the plant and the lab. Benzimidazole provides flexibility for building heterocyclic structures, but lacking the 2-hydroxy group means it’s less adaptable to electrophilic aromatic substitution and far less useful for polymer end-group modification. 2-Hydroxybenzimidazole allows unique derivatization profiles. This translates to options for more selective functionalization in nucleophilic aromatic substitution or for direct conversion to ethers or esters.
We’ve collaborated with polymer engineers working with specialty polyamides and polyesters. They share detailed performance data showing markedly better polymer-matrix compatibility when introducing 2-Hydroxybenzimidazole as a chain terminator or linker. The hydroxy group plays a pivotal role here, bringing improved solubility profiles during melt mixing and allowing for subsequent crosslinking opportunities. In practice, this means coatings, adhesives, and elastomers with enhanced chemical resistance and extended service lives.
The life sciences sector continually pushes for incremental improvements in both synthetic routes and intermediate stability. We’ve established joint projects with process chemists developing benzimidazole-based APIs, where even minor differences in starting material purity dictate the overall efficiency of synthesis. Chromatographic profiles of our 2-Hydroxybenzimidazole routinely show less than 0.2% total related impurities and residual solvent content below ICH Q3C thresholds—the result of granular attention during every production run.
It’s one thing to say product carries high purity; it’s another to prove each shipment reflects the same quality standard. In-house processing of 2-Hydroxybenzimidazole begins long before cyclization. Experienced staff double-check the specs for incoming o-phenylenediamine, control reaction times to avoid over-charring, and track minute-by-minute temperature curves. Any deviation shows up on our HPLC or GC data, prompting targeted re-work or, rarely, batch rejection—delivering the kind of consistency partners expect.
We use a closed-system approach to minimize airborne contamination and ensure safer handling, particularly during the reaction workup where trace solvents or byproducts can build up. Full-drum samples from each lot undergo not just chemical analysis, but visual and olfactory inspection by veteran technicians. More than once, this hands-on scrutiny has caught subtle changes that standard analytics can’t—such as faint yellowing that signals early-stage hydrolysis or minute traces of para-benzoquinone shift.
Moisture sensitivity remains a particular concern, especially for customers in humid climates. To address this, we use desiccant-lined packaging and nitrogen flush drums to maintain low water content until point of use. Shelflife studies conducted at 25°C/60% RH indicate stable performance for up to 18 months without detectable loss in purity or physical integrity.
Our role doesn’t end at the loading dock. Technical teams on the customer side routinely contact us with use-case feedback and troubleshooting needs. For example, an agrochemical formulator recently sought a way to streamline synthesis of a benzimidazole-facilitated crop protection agent. Working together, we optimized their hydroxy protection steps, reduced solvent usage, and minimized generation of problematic side products by providing 2-Hydroxybenzimidazole at stricter trace metal tolerances.
Other customers in pigment and dye manufacture value predictability; slight color changes or inconsistent solubility can disrupt batch processes downstream. Product engineers routinely relay the importance of particle size and particle morphology. We respond by customizing milling protocols and sieving granulation to align better with stir-in and solution processes. It’s this back-and-forth—listening, adapting, sometimes tweaking process parameters mid-campaign—that sets our approach apart from generic commodity suppliers.
A key part of responsible production involves environmental stewardship. Years ago, we transitioned to solvent recovery units that cut annual waste output by one-third. Effluents that once represented a disposal challenge now feed into an onsite catalytic oxidizer, reducing actual chemical oxygen demand below regional regulatory limits and improving the environmental footprint of 2-Hydroxybenzimidazole.
No two applications demand exactly the same grade of intermediate. Researchers working in pilot-scale pharma synthesis value ultra-pure lots, free from even faint halogen or metal traces. Large-volume pigment manufacturers focus more on bulk cost structure while maintaining robust color fidelity and solubility specs. We routinely adjust crystallization procedures and fine-tune drying times to meet divergent specs. Years spent collaborating with both small labs and global majors taught us that flexibility and responsiveness define a reliable manufacturer.
On request, we supply enhanced grades featuring certified low-halogen and low-sulfur content, especially for electronics-related end uses. These custom batches pass through high-sensitivity ICP-MS testing for elemental impurities and get bagged on a separate line to minimize cross-contamination risk. This work responds to the advanced needs of researchers who, for instance, seek benzimidazole-derived monomers for OLED and relevant optoelectronic applications, where a rogue ppm of iron or chloride disrupts device performance.
Supplying chemical intermediates to a global market throws up a barrage of logistical and compliance hurdles. Customers in the European Union demand full REACH registration and documentation; partners in North America expect complete traceability from raw material sourcing through to finished goods. Our compliance officers work with regulatory consultants to keep registration dossiers up to date and to provide full support for customer filings, especially important for pharma and agrochemical development programs.
Consistent export readiness means anticipating changes in hazardous goods classification, fulfilling packaging and labeling requirements, and maintaining safety stocks to handle unforeseen delays. We spent years building a supply chain that could get 2-Hydroxybenzimidazole from factory floor to customer warehouse with minimum friction—whether that means delivering in 25kg fiber drums, 250g research packs, or 1000kg bulk lots loaded direct to ISO containers.
User feedback matters more than any written specification. Sometimes the test comes from an unexpected angle: one batch headed to a specialty dye house exhibited slightly increased solidification in storage—a temperature and humidity control gap we didn’t initially account for. We took these concerns to the production floor, added shelf-stability evaluation points at new temperature and moisture levels, and adjusted our desiccant protocols. The result: defect rates dropped, and uptime increased, giving dye manufacturers the predictability they depend on.
Working with API developers, the key challenge connected to solvent residue. One customer flagged toxicity concerns related to residual DMF in early lots. We responded quickly, introducing extended vacuum stripping and switched to a cleaner ethanol-based workup step, all while monitoring output for new impurity profiles. On subsequent batches, GC-MS confirmed sub-ppm DMF traces, successfully alleviating ongoing regulatory headaches for our partners.
Another group in polymer compounding raised concerns about batch-to-batch consistency for melt index and color. Our team identified small but significant variations in crystallization cooling rates as the culprit. By standardizing batch cooling and retraining operators on post-crystallization drying procedures, we delivered a tighter, more predictable product that sped up formulation cycles for these customers by nearly 20%.
Direct experience informs our understanding that chemical differences often translate to real economic and performance impacts. Take benzimidazole, the parent compound, which offers versatility but lacks reactive functional groups for easy downstream functionalization. By contrast, 2-hydroxy-substitution at the second position enables direct etherification, esterification, and further substitution reactions that reduce both step count and risk in many syntheses.
Users frequently compare 2-Hydroxybenzimidazole with 2-methyl- or 2-amino-benzimidazoles. The hydroxy group is neither as acidic nor as nucleophilic as an amine, but its presence opens routes to different sets of derivatives—especially phenolic ethers and esters. In pigment chemistry, where stability under light and oxidative stress is essential, the 2-hydroxy is better suited to long-term performance. For polymerists, the hydroxy lends itself to direct covalent bonding and chain extension that amines often complicate through side reactions or uncontrolled cross-linking.
From an operational standpoint, we learned that 2-Hydroxybenzimidazole’s moderate solubility in polar solvents gives it an edge in multi-step synthesis by supporting facile purification and re-precipitation. Benzimidazole itself, by contrast, occasionally suffers from overly high solubility, extending solvent recovery times and contributing to downstream waste generation. Each of these nuances only fully emerged after cycles of hands-on experimentation, scale-up, and customer dialogue.
Chemical innovation keeps moving. Lately, we’re seeing 2-Hydroxybenzimidazole explored as a ligand in coordination chemistry, especially for transition metal catalysis in organic transformations. Synthetic chemists send feedback that the 2-hydroxy group supports alternative binding and redox activity compared to unsubstituted analogues, and our QA data backs them up: minor tweaks in particle size or residual water can meaningfully shift chelation performance in catalysis R&D projects.
Some R&D groups now investigate its role in stabilizing specialty resin formulations for electronics encapsulation and advanced composite materials. By providing batches screened for minimum ionic contamination, we enable these researchers to push ahead with new generations of fiber-reinforced plastics and PCB coatings. Feedback loops in these partnerships foster incremental improvements on both sides—ours in purification, theirs in performance benchmarks.
Manufacturing specialty intermediates isn’t static. Each customer request, each new regulatory guideline, and every batch that deviates in some small way from expectation pushes us to evolve. For 2-Hydroxybenzimidazole, that has meant introducing more robust process monitoring, tighter impurity control through advanced recrystallization, and expanded analytics covering everything from trace metals to non-routine side products.
We’re also aligning with broader industry shifts toward sustainable chemistry. Efforts to minimize waste by improving yield in the final cyclization step, switching to less hazardous solvents, and investing in renewable energy at the plant all carry forward into the footprint of every drum we ship. While the molecule remains the same, the path to producing it responsibly, efficiently, and predictably never stands still.
Our years spent handling, synthesizing, and refining 2-Hydroxybenzimidazole give us a perspective that outlasts market trends or commodity price swings. The fundamental difference between a manufacturer and any middleman comes down to accountability. We live with the choices we make—how strictly we screen raw materials, how closely we manage process variables, and how directly we engage with our customers when things go right or wrong.
High-purity 2-Hydroxybenzimidazole offers tangible advantages over similar compounds. Reliable manufacture, responsive adaptation to application feedback, and unwavering attention to detail in purity and physical properties distinguish this product from industry-standard grades. For partners in pharma, polymers, dyes, and beyond, it’s these daily practices—shaped by lessons learned and problems solved—that make our offering something more than a checklist of specifications. It is direct experience brought to bear, serving innovators around the world as they push materials science forward.