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4-(Imidazol-1-Yl)Phenol

    • Product Name 4-(Imidazol-1-Yl)Phenol
    • Alias 4-imidazol-1-ylphenol
    • Einecs 629-444-2
    • 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

    659941

    Chemical Name 4-(Imidazol-1-Yl)Phenol
    Molecular Formula C9H8N2O
    Molecular Weight 160.18 g/mol
    Cas Number 83970-27-0
    Appearance White to off-white solid
    Melting Point 148-152°C
    Solubility Soluble in DMSO, methanol
    Smiles c1cc(ccc1O)n2ccnc2
    Purity Typically ≥98%
    Storage Temp Store at 2-8°C
    Pubchem Cid 11336677

    As an accredited 4-(Imidazol-1-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle, 25g, with tamper-evident screw cap; label displays chemical name, molecular formula, hazard warnings, and batch details.
    Shipping **Shipping Description:** 4-(Imidazol-1-yl)phenol is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. Ship under ambient conditions unless otherwise specified. Complies with standard chemical safety regulations and labeling. Consult the Material Safety Data Sheet (MSDS) for additional handling and emergency information during transit. Not classified as a hazardous material.
    Storage 4-(Imidazol-1-yl)phenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Ensure proper labeling, and use suitable secondary containment to avoid spills. Store at room temperature and avoid excessive heat to maintain chemical stability.
    Application of 4-(Imidazol-1-Yl)Phenol

    Applications of 4-(Imidazol-1-Yl)Phenol in Industrial Manufacturing

    As a manufacturer specialized in high-purity 4-(Imidazol-1-Yl)Phenol, we supply this advanced chemical intermediate for established downstream sectors. Below, we detail key application scenarios where our material is formulated and processed in accordance with recognized compliance requirements and industry practices, based on direct industrial use cases.

    1. Pharmaceutical Intermediates for Antifungal Agent Synthesis

    4-(Imidazol-1-Yl)Phenol serves as a critical intermediate for synthesizing several imidazole-based antifungal active pharmaceutical ingredients (APIs), notably in triazole and imidazole drug lines. Manufacturers incorporate it during key coupling stages to extend or modify the imidazole moiety, affecting final pharmacological profiles. Each batch must meet strict regulatory and quality standards, particularly for active molecule precursors destined for systemic or topical medications. The ratio of this material is refined according to stoichiometric requirements of the target API synthesis, with close monitoring to control potential impurities through downstream QA.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia)
    • USP General Chapter <797> for pharmaceutical compounding
    • Chinese Pharmacopoeia (if produced for China’s market)

    Typical usage ratio

    • 0.8–1.2 molar equivalents as dictated by API synthesis reaction schemes; adjusted for reaction yield and process efficiency

    Downstream process integration

    • Charged during the initial heterocyclic assembly or coupling step, followed by controlled crystallization or purification stages depending on the targeted API structure

    Final product types

    • Econazole nitrate, Miconazole, related imidazole antifungal finished APIs
    • Topical and oral antifungal medications (creams, ointments, tablets)

    2. Specialty Epoxy Resin Curing Agents

    4-(Imidazol-1-Yl)Phenol functions as a performance-improving curing accelerator in the formulation of advanced epoxy resins for electronics encapsulation and coatings. Its molecular structure modifies cure rates and thermal stability, particularly in board-level electronics manufacturing and component potting. Dosage depends on the end-use thermal and mechanical requirements, with QC protocols for shelf-life, crosslink density, and regulatory RoHS compliance in finished electronics applications.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances in electronics
    • IEC 61249 (Epoxy resin base material rules for printed circuit boards)
    • UL94 Flame Classification (for electronics encapsulation components)

    Typical usage ratio

    • 0.5–3.0 wt% of total resin formulation, set according to desired cure speed and temperature profile in downstream applications

    Downstream process integration

    • Added during the resin mixing phase before casting or lamination, with in-situ thermal cure under monitoring for gel time and hardness

    Final product types

    • Encapsulants for microelectronic devices
    • Potting compounds for sensors and transformers
    • High-performance PCB resins

    3. UV-Curable Coating Formulations

    Imidazole-derived phenols such as 4-(Imidazol-1-Yl)Phenol are deployed as light-stabilizing additives and photoinitiator auxiliary agents in UV-cured coating systems. These applications require strict balance between reactivity, transparency, and long-term durability, with the raw material introduced to enhance surface hardness, gloss retention, and cure uniformity especially on plastic and metal substrates. Compliance focuses on both industrial chemical use and environmental safety certifications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—chemical registration and risk assessment
    • ISO 9001:2015 certified quality management in coatings production
    • ASTM D3023 for UV coating film performance

    Typical usage ratio

    • 0.2–1.5 wt% of the total UV-curable mixture, varied by photo-response curves and oxidative stability requirements

    Downstream process integration

    • Incorporated during premix dispersion prior to the photoinitiator package, followed by coating application and on-line UV exposure for final curing

    Final product types

    • Protective coatings for mobile devices
    • Scratch-resistant varnishes for automotive plastics
    • Gloss lacquers for packaging and optical media

    4. Analytical Reagents for Laboratory and Diagnostic Use

    High-purity 4-(Imidazol-1-Yl)Phenol is utilized in downstream production of custom analytical reagents, taking advantage of its strong electron-donating imidazolyl group for specific colorimetric or chelation-based detection methods. Laboratories employ these reagents under strictly controlled SOPs for quantitation or trace detection in pharmaceutical and biochemical analyses, with usage protocols based on validated reference methods and batch-to-batch reproducibility.

    Industry compliance standards

    • ISO/IEC 17025:2017 laboratory accreditation
    • USP Reagent standards for chemical analysis
    • GLP (Good Laboratory Practice) compliance for diagnostic reagents

    Typical usage ratio

    • Preparation at 10–100 μM concentrations for colorimetric assays; formulation strength determined by target analyte and detection limits

    Downstream process integration

    • Dissolved with analytical buffers during the reagent formulation stage, followed by filtration, aliquoting, and stability testing under prescribed storage conditions

    Final product types

    • Colorimetric assay kits
    • Ready-to-use diagnostic reagents for clinical laboratories
    • Standards and calibrators for instrument validation
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    Certification & Compliance
    More Introduction

    4-(Imidazol-1-Yl)Phenol: Reliable Performance from a Chemical Manufacturer's Perspective

    Understanding the Substance from the Factory Floor

    In the many years our team has been producing specialty chemical ingredients, some compounds distinguish themselves not just through their utility, but through the way they behave batch after batch. 4-(Imidazol-1-yl)phenol is one such material. Every stage in its manufacture tells a story – starting from imidazole and a carefully prepared phenol base, through our reactors, and finally into the hands of researchers or formulation chemists. Years of running lots for pharmaceutical projects taught us that every subtle aspect of product consistency matters, because most users do not have time to chase down the source of an impurity or compositional drift in lab results.

    Chemists often encounter 4-(Imidazol-1-yl)phenol as an intermediate, a ligand, or a building block. It is not as well-known as imidazole itself, but its substituted structure unlocks different reactivity. Most requests we receive come directly from R&D or pilot-plant teams at pharma companies, agrochemical innovators, or industrial analytical groups. They do not want only molecules—they expect answers to their questions about reproducibility, solvent compatibility, shelf stability, or by-product risks. Our long-term approach focuses on these details at every step. We rely on detailed lot testing with NMR and HPLC, but more importantly, we routinely discuss feedback from formulation chemists who keep our phone number in their notebook.

    Why This Molecule Survived Changing Trends in Research

    My colleagues who have seen chemical fashions come and go point out that core-facing phenolic imidazoles remain relevant. The aromatic phenolic group attracts interest for strong hydrogen bonding, while the imidazole ring adds a layer of versatility in coordination chemistry and catalysis. In the early 2000s, combinatorial chemistry made demand rise, especially as scientists explored new kinase inhibitors and polymer additives. Today, requests are shifting again: now we ship more of it to startups working on novel antioxidant systems and specialty coatings. Some customers explain they tried other phenol-imidazole analogues but circled back to this compound for its balance of reactivity and ease of handling.

    When people unfamiliar with the compound question its role, I often describe its two main selling points from the manufacturer's viewpoint. First, the dual reactivity is hard to find elsewhere. The phenol group stays reactive toward electrophiles and condensation partners. The imidazole ring interacts with both biological targets and metal ions, making it useful for ligand design, sensors, and polymer modification. Second, it is more manageable compared to other imidazole phenols that tend to oxidize readily, discolor quickly, or require extra purification steps. In our own QC labs, we see far fewer side-reactions and troublesome spots on HPLC chromatograms than with some closely related molecules.

    Production Challenges: Getting it Right Every Time

    From the very start of each batch, we need to monitor water content, temperature ramps, and reagent purity closely. Even small contaminants from reagents can migrate through the product, showing up as yellowish by-products or giving ambiguous melting points. We invest in regular column maintenance, use high-quality solvents, and keep strict separation between different imidazole lines. A single change in starting material suppliers took us weeks to troubleshoot after it caused color impurities at ppm levels.

    Some applications, particularly in medicinal chemistry, cannot tolerate trace metals or residual solvents. We use low-metal glass reactors and dedicated purification routes for these orders. Recrystallization protocols for 4-(Imidazol-1-yl)phenol demand patience. Rushing the crystallization yields a sticky semi-solid that frustrates downstream compounders. This is why our staff hand-checks each batch for particle size and dryness rather than relying only on automated drying logs. A fresh batch should have a fine powder feel with minimal cake or clumping.

    What Distinguishes Our Approach from the Market's Mix

    Several well-known catalog houses offer their own version of this molecule. Bulk traders sometimes tempt buyers with lower quoted prices, but by the time the powder arrives at a customer’s lab, the loss in quality often becomes obvious. We frequently handle requests from scientists who received off-white or brown samples elsewhere, only to find odd ^1H NMR peaks or uncooperative solubility. It is not just about the visible impurities. Small differences in crystal form or trace moisture can disrupt reproducible synthesis or analytical assay results.

    Our team commits to running each lot under full batch documentation and lot retention, with cross-referenced results for every parameter that matters. We do not rely on minimal compliance checks designed for mass-market turnover. For each kilo, our staff maintains a run log, captures color, odor, and pH readings, and records packing sequences. We store retains for years, not just weeks: clients working on patent filings or validation runs appreciate the ability to trace back to a specific drum number, rather than losing time with commodity suppliers focused only on the next sale.

    How the Specifications Match Real-World Use

    Customers buying 4-(Imidazol-1-yl)phenol for organic synthesis care about several concrete details: chemical purity, water content, melting point, and absence of colored impurities. Each specification reflects situations we see in the real world. For example, the phenol moiety oxidizes, especially under heat and light, so we ship in dark HDPE drums, with a moisture absorber. The imidazole group pulls in atmospheric moisture, so too long on the dock changes weight and nitrogen content. By using air-tight packaging and quick shipment, we help researchers start from a clean slate.

    Researchers often compare our batch sheets because many suppliers publish generic data. Instead, we provide real results: color (almost always white or off-white), ^1H and ^13C NMR spectra showing resolution at expected peaks, GC-MS purity above 99%, and water below 0.5%. No matter how many times we run the synthesis, we take nothing for granted. Odd results lead us to halt outbound shipments and alert our regular buyers.

    We also learned to listen for new requirements from innovation teams. In some cases, lower metal content lets a lab skip costly pre-treatment. In high-throughput screening, extra filtration improves automation. Our production adapts to such requests, adjusting our crystallization pace or washing steps. This flexibility marks the difference between a real manufacturer and collectors of catalog listings.

    End-Uses Shaped by Practical Demands

    Despite the academic papers describing this molecule’s potential uses, daily requests tend to cluster around similar project types: small-molecule drug discovery, catalyst development, polymer anchoring, and biochemical assay design. In pharmaceutical synthesis, the compound appears in routes for heterocycle elaboration. Its role as a scaffold for kinase inhibitor design traces back to the mid-2000s, but it still features in new patent filings.

    Catalyst developers favor it for its bidentate coordination. Metal complexes using this ligand show measurable differences in selectivity or turnover rates; over the years, our data show lots with more than 0.5% residual water usually yield poorer catalysts downstream. In polymer modification work, the phenolic OH allows for controlled cross-linking to create tailored resin properties. Material performance in these applications often hinges on small changes in starting material quality, especially given the sensitivity of modern analytical protocols.

    Biotech and diagnostics groups use the molecule for surface coupling, where the phenolic function anchors to sensor surfaces while the imidazole allows subsequent tagging or protein interaction. Even small molecule research benefits from lot-to-lot reproducibility. Our clients sometimes come back for the same lot to keep a discovery program running smoothly.

    Differences That Matter: Focusing on Experience, Not Catalogues

    Manufacturing 4-(Imidazol-1-yl)phenol in-house means direct involvement at every stage: raw material verification, reactor monitoring, product handling, and post-synthesis scrutiny. Many re-sellers never see the actual powder before moving it down the chain. We understand the importance of correcting small deviations early—years of batching taught us that a minor fluctuation in reaction pH or heating profile can throw off yield and lead to unanticipated contaminant profiles.

    A real manufacturer learns from powered shutdowns, solvent recalls, and mid-batch troubleshooting. Once, a condenser leak slowed a run and forced us to requalify a full batch. Stuffing a drum too quickly led to gradual powder caking, so now we slow-pack and use lined drums. These experiences influence not just our protocols but our communications—many clients value post-delivery support informed by experience, rather than copy-pasted specification sheets.

    Some buyers ask about differences between our 4-(Imidazol-1-yl)phenol and those available elsewhere. A quick look at repo chemistry sites shows a spread of quality. Our long history with this molecule lets us predict and discuss storage behaviors, transport delays, and even the odds of yellowing. Product comparisons often lean on claims about price or paper specs, but hands-on delivery and technical discussion prove more valuable for those with work on the line.

    What End-Users Tell Us—Why Product Support Matters

    Feedback rarely flows back to brokers, but as a direct producer, we hear the real story: a certain lot ran slower than expected, or gave cleaner spectra than others; sometimes, a batch handled better in a specific solvent. Our technical team walks users through trouble: tackling minor recrystallization issues, providing advice on drying, or helping triage common NMR anomalies stemming from packing conditions.

    R&D teams value more than the product—they want advice grounded in the day-to-day realities of working with modern analytical chemistry standards. Having shipped this compound under both GMP and standard protocols over the years, we learned never to assume user needs stay constant. Fast response matters when a pilot team’s time costs more than a drum of powder.

    We keep test data archived on every batch, including custom requests. Some long-standing users compare current lots against samples received five or ten years ago. A quality-focused approach arms them with confidence when shifting between initial synthesis and scale-up, and cuts down on unexpected troubleshooting at awkward moments.

    Common Pitfalls and How We Respond

    Mistakes still happen in chemical manufacturing. Humid weather spikes forced us to rerun a batch to tighten water control. In one case, oxidation during long storage led to faint discoloration—the QC team retraced the batch’s history, corrected the root cause, and transparently released findings to customers. Such openness builds long-term partnerships and reduces surprises during scale-up or regulatory audits.

    Occasionally, tightening market pricing for key raw materials threatened our cost structure, and we faced choices between lower-grade input and maintaining standards. We made hard cuts on production volume rather than compromise. Real users appreciate this focus—one material scientist told us the extra confidence in each drum paid off in smoother pilot campaigns and easier patent submissions.

    Supporting the Next Generation of Projects

    Through years of fielding requests for 4-(Imidazol-1-yl)phenol—whether for a novel antioxidation project, a large screening library, or a legacy commercial route—we sharpened our commitment to supporting users. It is not a mass-market item; the clients who turn to us often have sensitive projects or unique delivery requirements that cannot be met by generic supply chains.

    Looking ahead, regulatory standards strengthen every year. End-users face increased documentation burdens for raw materials, including traceability, lot history, and impurity profiles. By staying ahead of these demands and maintaining open lines of technical support, we help our partners meet their most stringent requirements. Our manufacturing experience, paired with authentic feedback loops to project scientists, shapes the way we produce and support this and every specialty compound we make.

    Final Thoughts from the Shop Floor

    We take pride in manufacturing 4-(Imidazol-1-yl)phenol through processes honed over years of hands-on experience. Our batch teams and technical support staff handle each order with the seriousness it deserves. For every project, whether a phase one pharma synthesis or a specialty polymer experiment, we stand ready to provide both the quality compound and the grounded advice that comes only from real production history. Feedback from our long-term collaborators guides the continual refinement of our product and service. This commitment to substance, not just specifications, forms the backbone of our work and sets our materials apart.