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2-Hydroxybenzimidazole

    • Product Name 2-Hydroxybenzimidazole
    • Alias 2-(1H-Benzimidazol-2-yl)phenol
    • Einecs 219-467-4
    • 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
    VTB
    Specifications

    HS Code

    480373

    Cas Number 615-11-2
    Molecular Formula C7H6N2O
    Molecular Weight 134.14 g/mol
    Iupac Name 1H-benzo[d]imidazol-2-ol
    Appearance White to off-white powder
    Melting Point 290-295°C
    Solubility In Water Slightly soluble
    Density 1.38 g/cm³
    Smiles OC1=NC2=CC=CC=C2N1
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing 2-Hydroxybenzimidazole, 25g: Supplied in a sealed amber glass bottle with a tamper-evident cap, labeled with safety information and batch details.
    Shipping 2-Hydroxybenzimidazole is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical is classified as non-hazardous, but standard laboratory precautions apply. Packaging must comply with local and international transport regulations to prevent spillage or contamination. Ensure proper labeling and documentation accompanying the shipment for safety and regulatory compliance.
    Storage 2-Hydroxybenzimidazole 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. Protect it from moisture, direct sunlight, and sources of ignition. Proper labeling and secure placement are essential to prevent accidental exposure or spillage. Store at room temperature and follow all relevant safety guidelines.
    Application of 2-Hydroxybenzimidazole

    Applications of 2-Hydroxybenzimidazole in Industrial Manufacturing

    As a direct manufacturer of high-purity 2-Hydroxybenzimidazole, we supply this specialty raw material to global industrial customers across established downstream sectors. Our experience covers stringent compliance requirements and process integration needs, ensuring real-world application value for formulators and end producers. Below we detail core application areas strictly based on verified industry practice.

    1. Rubber Vulcanization Accelerator for Industrial Elastomers

    In the production of tire compounds, automotive hoses, seals, and technical molded goods, 2-Hydroxybenzimidazole functions as a secondary accelerator, specifically boosting the activation of sulfur-based curing systems. This additive sharpens cure speed and enhances heat aging resistance, complementing primaries like thiuram or sulfenamides. It integrates efficiently in masterbatch mixing, where formulation technologists adjust the addition rate to balance scorch time with final mechanical performance, ensuring compounders meet the exacting demands of OE automotive and engineered elastomer markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems (for rubber compounding controls)
    • ASTM D3182 (Rubber—Compounding Ingredients—Standard Practice for Mixing)
    • REACH Regulation (EC) No 1907/2006 compliance for additives in the EU
    • China GB/T 5574—Rubber Accelerator Safety & Technical Standards

    Typical usage ratio

    • 0.1%–0.5% by weight of total rubber formulation; varies based on sulfur/accelerator system and targeted cure characteristics

    Downstream process integration

    • Added during the internal mixing or open mill stage after mastication; thoroughly blended with fillers, oil, and other accelerators prior to forming and vulcanization

    Final product types

    • PCR/LTR/Earthmover tires
    • High-performance oil seals and gaskets
    • Rubber conveyor belts
    • Anti-vibration automotive parts

    2. Corrosion Inhibitor Additive for Industrial Water Treatment

    Downstream water treatment formulation houses use 2-Hydroxybenzimidazole as a chelating and passivation agent, particularly within closed-loop cooling circuits, boiler feeds, and process water systems exposed to multi-metal alloys. Its role is to form stable, adherent protective layers on ferrous and non-ferrous metal surfaces, suppressing both anodic and cathodic reactions responsible for scaling and pitting. Adoption in this sector is driven by the chemical’s efficacy under high-temperature and variable pH, extending asset life and minimizing unplanned shutdown costs for refineries and power stations.

    Industry compliance standards

    • ASME Boiler and Pressure Vessel Code (Boiler Chemical Treatment section)
    • ANSI/NSF Standard 60 (when used in potable water-compatible programs)
    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) for inhibitors
    • China HG/T 2380—Technical Criteria for Water Treatment Chemicals

    Typical usage ratio

    • 5–30 ppm (parts per million) in recirculating water; adjust based on total dissolved solids, flow rates, and metallurgy

    Downstream process integration

    • Dosed directly into water circuits via metering pumps, typically synergized with phosphonates and azoles during formulation of multi-component inhibitor blends

    Final product types

    • Recirculating cooling water inhibitors
    • Boiler water treatment formulations
    • Closed-circuit anti-corrosion packages
    • Integrated scale/corrosion prevention concentrates

    3. Pharmaceutical Intermediate for APIs and Bulk Drugs

    Established pharmaceutical active ingredient (API) manufacturers employ 2-Hydroxybenzimidazole as a key heterocyclic synthon in the synthesis of benzimidazole-family pharmaceuticals, including various antiviral, antifungal, and gastroprotective molecules. Process chemists leverage this intermediate in step-growth procedures such as nucleophilic aromatic substitution, optimizing reaction yields and selectivity under GMP-controlled batch operations. Quality assurance requires full traceability and impurity profiling, as regulatory filings hinge on reproducible impurity profiles and consistent batch reproducibility.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as per ICH Q7 guidelines
    • Ph. Eur. (European Pharmacopoeia) / USP monograph standards for APIs
    • DMF (Drug Master File) processes under US FDA 21 CFR Part 314
    • China Pharmacopoeia (ChP) Part II compliance for raw materials

    Typical usage ratio

    • Stoichiometric amount coordinated to desired active structure; precise ratio determined by downstream molecule target (e.g., one molar equivalent per API core unit)

    Downstream process integration

    • Incorporated as a principal building block during the heterocyclization or process-specific coupling step under controlled temperature, solvent, and catalysts; implemented in both pilot plant and industrial API runs

    Final product types

    • Benzimidazole-based proton pump inhibitors (e.g., omeprazole derivatives)
    • Antifungal imidazoles
    • Antiviral agents featuring substituted benzimidazoles
    • Bulk intermediates for CDMO (contract drug manufacturing) projects

    4. Copper Corrosion Inhibitor in Engine Coolant Formulations

    Formulators of automotive and industrial coolant fluids incorporate 2-Hydroxybenzimidazole specifically to prevent copper and copper-alloy corrosion in engine blocks, radiators, and heat exchangers. The additive forms a persistent barrier film that inhibits ion migration and galvanic cell formation, offering reliable protection even at varying ethylene glycol concentrations and extended high-temperature service. Compatibility studies ensure no adverse interaction with other inhibitors such as silicates, benzoates, or carboxylates, supporting its inclusion in multi-metal safe blends required by OEM coolant specifications and extended life coolant standards.

    Industry compliance standards

    • ASTM D1384—Standard Test Method for Corrosion Testing of Engine Coolants
    • SAE J1034 (Coolant Test Procedures)
    • OE manufacturer technical standards (GM 6277M, VW TL 774 series)
    • ISO 22241 (for SCR system compatibility in coolant blends)

    Typical usage ratio

    • 15–50 mg/L in finished coolant; dosage optimized based on copper surface exposure, coolant change intervals, and system operating temperature

    Downstream process integration

    • Dissolved in glycol-water concentrate during bulk blending; subject to homogenization before packaging into ready-mix or concentrated engine coolants

    Final product types

    • OEM-approved engine coolants (pre-mix and concentrate)
    • Heavy-duty diesel antifreeze
    • Industrial chiller and heat transfer fluids
    • Passenger car and truck radiator fluids

    5. Analytical Reagent in Metal Ion Complexation and Detection

    Analytical laboratories and diagnostic technology developers use 2-Hydroxybenzimidazole as a selective chelating agent and chromogenic reagent for trace metal ion determination in environmental, pharmaceutical, and food compliance testing. Its high complexation affinity with transition metals such as Fe(III) and Cu(II) underpins its use in spectrophotometric assay development. Rigorous lot control and documentation ensure reliable absorbance response and detection limits, critical for routine regulatory screening and quality control protocols in accredited labs.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing and Calibration Laboratories)
    • EPA Methods 200.7 and 200.8 (ICP-AES and ICP-MS Sample Preparation)
    • USP <231> Heavy Metals Testing (for ingredient/water analysis)
    • FDA 21 CFR Part 58 Good Laboratory Practice (GLP) for test results

    Typical usage ratio

    • Reagent concentrations range from 0.01–0.1% (w/v) in analytical preparation; adjusted by sample matrix and target detection limit per method

    Downstream process integration

    • Added during sample pretreatment or directly to colorimetric assay mixtures, often followed by controlled pH adjustment and incubation for endpoint reading

    Final product types

    • Trace metal detection kits
    • Diagnostic colorimetric reagents
    • Instrument calibration standards for environmental labs
    • Pharmaceutical and food sample test kits
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    Certification & Compliance
    More Introduction

    Introducing 2-Hydroxybenzimidazole: Insights and Practical Considerations

    In labs and production sites across the world, the search for reliable heterocyclic compounds remains a daily part of research and industry. Among these, 2-Hydroxybenzimidazole stands out as more than just a link in a supply chain—it opens the door to new chemistry for many teams. My experience with this compound has brought to light its remarkable stability and value in applications that call for both precision and dependability.

    Understanding the Fundamentals of 2-Hydroxybenzimidazole

    2-Hydroxybenzimidazole carries the molecular formula C7H6N2O and often appears as a pale, crystalline powder. Its chemical structure, placing a hydroxyl group on the benzimidazole ring, gives it a character distinct from the unsubstituted benzimidazole. That extra functional group can determine the path of an entire synthesis, letting downstream chemistry access new possibilities. The ability to tweak physical or electronic properties with such simple modifications is one of the joys of organic chemistry, and 2-Hydroxybenzimidazole shows up just where a little extra control is required.

    The Role of 2-Hydroxybenzimidazole in Research and Industry

    Medicinal chemists see this compound as an intermediate with significant promise. Its unique skeleton, combined with that hydroxyl side, means it pops up in literature for synthesizing pharmaceutical agents with biological activity. Antimicrobial, antiviral, or anticancer research often passes through a benzimidazole stage. If you’ve spent time in a synthetic chemistry lab, you might have found yourself grateful for how clean this compound recrystallizes and how easily it integrates into multi-step syntheses without losing structural integrity. No small feat when a reaction pathway can teeter off course at any moment.

    Beyond pharmaceuticals, 2-Hydroxybenzimidazole matters in dye development, corrosion inhibitors, and as a ligand for coordination chemistry. The practical upshot is that it helps materials scientists and industrial chemists push their studies further, whether that's in building complex molecular assemblies or preventing rust in metal processing plants. This compound’s stability, both chemically and thermally, makes it valuable for any process that will see harsh conditions or lengthy storage. It doesn’t break down or lose its punch simply from sitting on a shelf or getting tossed between flasks—something every lab tech can appreciate.

    Model, Purity, and Specifications: What You Get

    When talking about models, most users refer to the compound’s grade and purity. In many cases, you’ll see high-performance liquid chromatography (HPLC) confirming a purity over 98%. That number means a lot for researchers. In my years managing lab inventories, I’ve noticed time and again that the small percentage points between a “research grade” bottle and a lower-purity alternative save headaches during analytics. Side reactions fall off, clean spectra make analysis straightforward, and you spend less time troubleshooting unexplained results. Many suppliers offer batches ranging from small amber glass vials for R&D to multikilogram drums for industrial use, giving flexibility based on demand.

    Physical specs highlight that 2-Hydroxybenzimidazole doesn’t attract too much moisture, stores well under standard cool, dry conditions, and dissolves readily in common polar solvents like DMSO and ethanol. This keeps handling simple, and means you don’t fight with solubility during downstream transformations or assays. I’ve worked with compounds that gunk up equipment or demand oddball solvents—this isn’t one of them. That practical ease carries over no matter which brand or model ends up on your shelf.

    Comparing 2-Hydroxybenzimidazole to Analogues and Substitutes

    Look at benzimidazoles with different functional groups, and you’ll notice how the position and type of substituent drive reactivity and selectivity. Take 2-hydroxy versus 1-hydroxy or non-hydroxylated forms: that difference, slight by the standards of structural diagrams, can reshape biological activity and selectivity in drug leads. My work on kinase inhibitor analogues proved this point firsthand, where shifting a single group altered the reaction kinetics and downstream pharmacology. For folks developing coatings or dyes, small variations in the aromatic nucleus make all the difference in lightfastness and solubility.

    Some try 2-aminobenzimidazole or benzimidazole-5-carboxylic acid as alternatives, betting on related reactivity or binding affinity. These can fill similar roles, but the hydroxyl group’s hydrogen-bonding capacity and nucleophilic tendencies give 2-Hydroxybenzimidazole a leg up in certain coupling reactions or chelation. I’ve seen this matter most in ligand work, where you want to wrangle metal ions for catalysis or complex building. Where another benzimidazole might fall short, this version steps up and bridges coordination sites smoothly, often improving yields and selectivity for downstream products.

    Challenges and Considerations in Use

    Juggling shelf life, batch consistency, and regulatory thresholds, buyers and users face clear choices about which benzimidazole derivative to keep on hand. I’ve run into corners where purity slips and analytical results get fuzzy—often traced back to low-quality material brought in to cut costs. With 2-Hydroxybenzimidazole, cGMP-grade lots and certificates of analysis can make or break compliance in pharmaceutical workflows. Having an unambiguous analytical profile isn’t just red tape; it smooths out supply chains and keeps regulatory inspectors off your back. Teams that skimp on documentation or traceability soon see the cost in recalls or failed audits.

    Another factor is safe handling. While 2-Hydroxybenzimidazole doesn’t bring the acute risks of volatile organic compounds or bulk corrosives, it calls for reasonable lab safety. Dust masks and gloves suffice in most settings, with disposal following standard organic waste streams to avoid environmental release. I’ve found that clear protocols and training—especially for interns or casual users—reduce accidents and keep the workflow efficient. The low odor and predictable melting range reduce the drama often linked to more volatile heterocycles.

    Why 2-Hydroxybenzimidazole Matters Today

    The rush toward new therapeutics and advanced materials keeps demand for high-quality intermediates high. In my time supporting pharmaceutical developers, I’ve watched 2-Hydroxybenzimidazole anchor more than a handful of research breakthroughs. Whether it’s serving as a building block for enzyme inhibitors or as a stabilizer in anti-corrosive coatings, the practical value shows up in outcomes, not just batch records. Research teams often share case studies highlighting successful scale-ups, citing robust yields and minimal troubleshooting. Knowing a compound will “work as advertised” frees both bench chemists and decision-makers to focus on innovation instead of technical fires.

    Material sustainability has become a key concern, especially as regulations tighten. Many older compounds fail to meet modern safety or environmental rules, but 2-Hydroxybenzimidazole aligns well with these expectations. Low toxicity, clean decomposition, and absence of heavy metals mean fewer barriers for approval and less long-term environmental risk. In my own sustainability initiatives, switching to cleaner intermediates often granted easier passage through internal review and community scrutiny.

    Pushing Boundaries with 2-Hydroxybenzimidazole

    The constant need for better ligands and novel pharmacophores makes compounds like this hard to replace. Chemists at the bench and in management both want tools that perform without expensive side effects—literally or figuratively. As green chemistry pushes for milder conditions and safer workflows, 2-Hydroxybenzimidazole’s moderate reactivity shines. It opens the door to one-pot syntheses and catalyst recycling, streamlining efforts in both exploratory and production settings. I’ve collaborated with synthesis teams who use it to cut cycle times and waste, all while hitting tighter purity specifications needed for advanced pharmaceuticals and diagnostics.

    It doesn’t hurt that the supply chain for 2-Hydroxybenzimidazole has matured. Reliable vendors deliver consistent batches. Supply disruptions remain rare compared to niche heterocycles or those requiring costly starting materials. In my experience, this reduces project risk and keeps process optimization focused on real performance gains—not paperwork or procurement headaches. The straightforward synthesis, often starting from o-phenylenediamine and salicylic acid, shortens lead times and keeps costs in check.

    Building on a Strong Foundation

    One of the main reasons I continue to recommend 2-Hydroxybenzimidazole is how it scales from the bench to pilot plant. I’ve watched it move through the R&D pipeline, scale up in 100-gram test runs, and land in kilogram-scale reactors without demanding a rewrite of protocols or workflows. That kind of flexibility makes life easier for chemical engineers as well as laboratory scientists. Variable reaction parameters don’t throw it off track, and both standard glassware and automated processes churn out product with minimal hiccups.

    For quality control teams, routine analytical methods such as NMR, IR, and HPLC provide clear fingerprints for both identification and purity checks. The compound behaves predictably during assessment, removing the guesswork that often drags out batch release or blocks shipments to clients. Having spent years bridging R&D labs and production, I’ve seen such properties take the sting out of scale-ups and repeated syntheses, which often catch less robust intermediates by surprise. That predictability saves both time and money, two resources always in short supply in weighty projects.

    Innovating with 2-Hydroxybenzimidazole in Pharmaceutics

    Developers focused on small molecule drugs keep returning to this intermediate. Its role in antiviral agents and kinase inhibitors crops up throughout patent databases and research articles. Given rampant infectious disease and pressing oncology needs, having dependable intermediates speeds up preclinical testing. In my discussions with process chemists, reliable payload handlers and consistent conversion rates often mean fewer headaches, less batch reprocessing, and tighter regulatory circles. Formulation scientists also appreciate the compound’s moderate logP and favorable pKa, which can ease the path to acceptable bioavailability for finished drugs.

    Interest in green and biocompatible molecules puts pressure on companies to review their ingredient choices. 2-Hydroxybenzimidazole’s benign profile and compatibility with aqueous synthesis routes have helped answer calls for cleaner, safer products. I’ve witnessed pharma partners win internal approval on new drug candidates partly by pointing to intermediates that don’t trigger regulatory pushback. The smoother journey from discovery to development keeps companies agile and nimble as they bring therapies to a demanding global market.

    Applications in Material Science and Industry

    Beyond health and medicine, application areas for 2-Hydroxybenzimidazole continue expanding. Researchers pushing boundaries in optical materials, polymers, and corrosion science tap its unique binding and electronic properties. In dye chemistry, it gives bright, consistent hues and holds up under adverse lighting or chemical conditions. Many projects I’ve shadowed in industrial chemistry focused on metal plating or surface treatments cite the value of heterocycles in achieving uniform, robust coatings. That tiny structural twist—the hydroxyl—nudges metal ions into place, making the difference between a promising prototype and a failed commercial product.

    Complexation chemistry also benefits from this molecule. Scientists assembling catalysts or metal-organic frameworks appreciate ligands that deliver both electronic flexibility and geometric fit. My own time in a catalysis lab drove home the value of reliable ligands: fewer purification steps, robust activity, and faster cycles. Time spent optimizing these systems doesn’t disappear chasing analytic ghosts or off-target reactions, letting teams drive innovations where they’re needed most. Industrial clients across coatings, electronics, and materials science echo the same priorities—outcomes tied to reproducible, well-characterized components.

    Paving the Way for Sustainable Chemistry

    Modern chemical practice hinges on sustainability and risk reduction as much as on cost savings. Lab leaders and production managers must now weigh more than just reactivity—they balance lifecycle, end-of-life, and supply assurance considerations. 2-Hydroxybenzimidazole stands up well when measured against these imperatives. It avoids some of the hazards that tar legacy intermediates with regulatory red flags. Low volatility, manageable toxicity, and a clear path for controlled disposal reduce both incident risk and long-term liability. That’s not just a compliance issue—it’s about building trust with internal stakeholders and external customers alike.

    Instituting more sustainable chemistry has called for practical decisions. Teams looking to shrink their environmental footprint have replaced more hazardous benzimidazole derivatives with 2-hydroxy variants, realizing improvements not only in regulatory scores but also job satisfaction and morale. I’ve seen these shifts translate into streamlined workflows, smoother interactions with regulatory agencies, and faster product launches, all while maintaining the technical quality needed for brand protection and end-user safety.

    Future Potential and Ongoing Research

    Chemistry doesn’t stand still, and neither does the investigation of derivatives like 2-Hydroxybenzimidazole. Current academic research explores new pharmaceutical leads, photostable dyes, and chelation techniques built on this backbone. Each year brings fresh methods for functionalization and new examples of bioactivity, reinforcing the role of benzimidazoles as privileged scaffolds in chemical discovery. Industrial collaborations with academic partners often focus on applications that square the circle: high performance, low risk, and scalable supply chains. The consistent performance of 2-Hydroxybenzimidazole in these contexts keeps it on the shortlists of both old-school chemists and next-generation innovators.

    The next decade may yet reveal new fields where benzimidazole derivatives help solve global challenges. Advances in personalized medicine, safer materials for electronics, and environmental remediation continue to draw on the compound’s flexible chemistry and clean safety record. Drawing from my experience sitting in project planning meetings, a reliable, general-purpose intermediate never loses value. Teams equipped with solid starting points can shift gears as project goals evolve, meeting the demands of customers, regulators, and end users alike.

    Bringing It All Together

    Reflecting on the journey of 2-Hydroxybenzimidazole from a niche academic interest to a practical mainstay in research and industrial labs, one lesson stands out—dependability matters just as much as innovation. When a compound offers both, it earns a lasting place in the chemical toolbox. Its ability to provide consistent results, safe handling, and diverse utility underpins successful research and product launches across disciplines. With the pace of modern science, the ease of integrating 2-Hydroxybenzimidazole into workflows lets teams spend less time firefighting and more time creating. In the ongoing quest for better solutions in chemistry and beyond, that practical advantage stands out.