Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Methyl-2-Phenyl-1H-Imidazole

    • Product Name 4-Methyl-2-Phenyl-1H-Imidazole
    • Alias 4-Methyl-2-phenylimidazole
    • Einecs 620-332-8
    • 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

    636496

    Chemical Name 4-Methyl-2-phenyl-1H-imidazole
    Molecular Formula C10H10N2
    Molar Mass 158.20 g/mol
    Cas Number 1448-80-4
    Appearance White to off-white solid
    Melting Point 87-90 °C
    Solubility In Water Slightly soluble
    Smiles Cc1nc([nH]c1)c2ccccc2
    Inchi InChI=1S/C10H10N2/c1-8-11-9(12-10(8)2)7-5-3-4-6-7/h3-6,12H,1-2H3

    As an accredited 4-Methyl-2-Phenyl-1H-Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Methyl-2-Phenyl-1H-Imidazole is supplied in a sealed 25g amber glass bottle with a printed hazard and identification label.
    Shipping 4-Methyl-2-Phenyl-1H-Imidazole is securely packaged in sealed containers to prevent contamination and degradation. It is shipped according to standard regulations for laboratory chemicals, typically via ground or air transport, labeled appropriately with hazard information. Temperature and humidity controls are maintained if required to ensure chemical stability during transit.
    Storage 4-Methyl-2-Phenyl-1H-Imidazole should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and excessive heat. Always label the container clearly and handle the chemical using appropriate personal protective equipment.
    Application of 4-Methyl-2-Phenyl-1H-Imidazole

    Applications of 4-Methyl-2-Phenyl-1H-Imidazole in Industrial Manufacturing

    4-Methyl-2-Phenyl-1H-Imidazole demonstrates valuable functional properties across multiple established chemical manufacturing sectors. As a direct producer, we ensure every batch meets the specific application needs of downstream users active in pharmaceuticals, photoinitiators, agrochemicals, polymer modifiers, and specialty paints. Below, we outline real industrial scenarios where our material plays a critical role, detailing each segment’s compliance standards, formulation ratios, process integration, and finished product types.

    1. Pharmaceutical Intermediates: Imidazole-Based Antifungal Synthesis

    This imidazole derivative enters the synthesis pathway of triazole and imidazole antifungal agents, where it acts as a key intermediate for building critical heterocyclic motifs. In active pharmaceutical ingredient (API) manufacturing, its functional group supports ring closure steps and confers enhanced selectivity for target molecules such as ketoconazole analogues.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • EP/USP/JP pharmacopoeial purity requirements for intermediates
    • WHO GMP for pharmaceutical raw material handling

    Typical usage ratio

    • Mole-to-mole basis: typically 1.0–1.2 equivalents per condensation or cyclization step, adjusted for process scale and target yield

    Downstream process integration

    • Feeds directly into stepwise organic synthesis after halogen exchange or Grignard formation; introduced at controlled temperature and pressure, often in sealed reactors to manage volatile byproducts

    Final product types

    • Triazole antifungal drug intermediates (e.g., fluconazole synthons)
    • Imidazole-based API core structures
    • Pharmaceutical-grade synthesis intermediates for specialty antimicrobials

    2. Photoinitiators for UV-Cured Coatings and Inks

    Downstream formulators use this imidazole structure as a key building block in the creation of multi-component photoinitiator systems, supporting free-radical polymerization when exposed to UV light during printing ink and coatings manufacturing. Its electron-rich heterocycle improves photo-reactivity and spectral absorption in custom photoinitiator blends.

    Industry compliance standards

    • REACH (EC Regulation No 1907/2006) registration for industrial safety
    • ISO 9001:2015 Quality Management for specialty chemicals production
    • Swiss Ordinance on Materials and Articles in Contact with Food (for food packaging inks, indirect)
    • ASTM D7767-11 (Standard for UV-Curable Ink Ingredients)

    Typical usage ratio

    • 0.1–1.5 wt% in the overall UV-curable formulation; precise level adjusted for ink film thickness and curing energy density

    Downstream process integration

    • Blended into photoinitiator premix during masterbatch production, followed by dispersion into prepolymer or oligomer base; subjected to QC testing for curing response and migration

    Final product types

    • UV-cured printing inks for packaging and labels
    • Industrial UV coatings for electronics and automotive parts
    • High-performance 3D printing resins

    3. Agrochemical Synthesis: Imidazole-Linked Fungicides

    Producers of specific systemic fungicides use this compound as a coupling and condensation agent in the assembly of active imidazole rings. Its methyl and phenyl groups increase efficacy against fungal pathogens in target crops while helping maintain chemical stability during formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (agrochemical intermediates)
    • ISO 17025:2017 (Testing and calibration laboratories, for QC)
    • EU Regulation 1107/2009 (Plant Protection Products Authorization)

    Typical usage ratio

    • Stoichiometric addition, 0.8–1.2 equivalents per target active molecule, based on specific crop protection formula and synthetic pathway

    Downstream process integration

    • Employed in a controlled reactor step for fungicide core ring construction, followed by extraction, crystallization, and formulation into technical concentrates

    Final product types

    • Commercial imidazole fungicide actives (e.g., prochloraz derivatives)
    • Crop protection technical concentrates
    • Broad-spectrum agricultural fungicide formulations

    4. Polymer Additives: Curing Catalysts for Epoxy Resins

    Processors incorporate this imidazole into epoxy resin systems as a latent curing catalyst. It enhances polymer cross-linking speed at targeted cure temperatures, minimizes yellowing, and improves the mechanical performance of molded and laminated end products.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for Chemicals)
    • UL 94 (Flammability of Plastic Materials)
    • ISO 9001:2015 (Resin manufacturing and QC)
    • RoHS Directive (2011/65/EU) for electronics-related epoxy compounds

    Typical usage ratio

    • 0.1–0.5 phr (parts per hundred resin) in thermal or UV-cured epoxy blends; ratio selected based on degree of latency required in application

    Downstream process integration

    • Dispersed into resin system during masterbatch mixing, then subjected to vacuum degassing and pre-curing hold before lamination or molding

    Final product types

    • Epoxy encapsulants for electronic circuits
    • Laminates for PCB substrate manufacturing
    • Industrial adhesives and structural composites

    5. Specialty Paints: Corrosion-Resistant Primer Formulations

    This imidazole ring structure finds application in anti-corrosive primer formulations where it acts as a complexing agent, improving adhesion and creating protective layers on metal substrates. Downstream paint manufacturers rely on its performance in environments requiring extended durability and specific chemical resistance.

    Industry compliance standards

    • ASTM D3276 (Standard Guide for Paint Application)
    • ISO 12944 (Corrosion Protection of Steel Structures by Protective Paint Systems)
    • REACH chemical safety assessment
    • ISO 9001:2015 (Paints and coatings QC)

    Typical usage ratio

    • 0.2–1.0 wt% relative to binder solids, depending on metal type and corrosivity rating

    Downstream process integration

    • Incorporated during pigment grind, followed by let-down and dispersion in aqueous or solvent-based systems; batch QC includes accelerated corrosion testing

    Final product types

    • Corrosion-resistant primers for marine and offshore structures
    • Primers for automotive and heavy equipment coatings
    • Protective paints for chemical processing plants
    Free Quote

    Competitive 4-Methyl-2-Phenyl-1H-Imidazole prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Getting to Know 4-Methyl-2-Phenyl-1H-Imidazole from the Chemist’s Bench

    A Practical Introduction from the Manufacturer’s Perspective

    Handling specialty imidazole derivatives brings its own set of technical puzzles and rewards. In our plant, 4-Methyl-2-Phenyl-1H-Imidazole commands attention among the crowd of heterocyclic compounds. This imidazole stands out for the balance it strikes between molecular stability and functional group reactivity. Workflows in organic synthesis, material sciences, and pharmaceutical development often call for a robust backbone with selective modification options. In practice, this molecule repeatedly serves as a flexible starting point and a durable intermediate.

    Lab-scale preparation gives a hint of its behavior, but industrial manufacture uncovers its full character. The phenyl ring enhances its pi-electron conductivity, so researchers look at it closely when seeking nuanced performance in electronics or as building blocks for receptor ligands. The methyl group at the four position doesn’t overwhelm the system with bulk, so reaction routes remain open, and downstream transformations rarely clog up when using this imidazole as a substrate.

    Specifications Built on Process Experience

    Batch-to-batch consistency remains a central guiding star for the plant floor and QA lab. After years of scaling this compound, we deliver 4-Methyl-2-Phenyl-1H-Imidazole in a form tailored for actual lab and plant processes: crystalline powder, finely milled, white to faintly off-white by careful control of the final recrystallization and drying. Moisture control isn’t just part of the protocol; it proves itself in the way the powder flows out of bulk containers, leaving minimal residues and staying free of unwanted agglomeration.

    Our product model, catalogued as 4M2PHI-01, demonstrates a melting range that signals purity above 98%. High-performance liquid chromatography and rigorous GC/MS checks screen for isomers and side products. Not every manufacturer pushes for such a narrow impurity profile, but longer experience taught us that just a hint of contaminant amines or under-reacted starting material sends headaches down the pipeline in pharmaceutical and materials projects.

    Bulk density, particle size, and residual solvent content might seem like dry technical details from the outside. Inside the plant, these factors play into everything from transport safety to how evenly the product dissolves or reacts in larger reactors.

    Why Do Chemists Choose 4-Methyl-2-Phenyl-1H-Imidazole?

    Every organic chemist reading a raw material list starts with structure and reactivity, then pivots to reliability and sourcing. This imidazole lets designers build diversity into libraries and synthesize target candidates with precision. Small tweaks at the methyl position don’t derail reaction kinetics, while the phenyl group creates routes for further aromatic substitutions or nucleophilic attacks. Unlike unsubstituted imidazole, which sometimes leads to run-away polymerization or hinders selectivity, the 4-methyl-2-phenyl variant keeps side pathways in check.

    Talking with formulation chemists, you quickly find they respond to the solid-state properties of this compound. Its melting point neither drifts too low nor forces intensive heating—so small-scale and pilot operations run smoothly. Synthetic routes to pharmaceutical intermediates profit from the well-defined reactivity. Those working in material sciences appreciate that the phenyl-methyl pattern doesn’t introduce unpredictable electronic effects but strengthens overall molecular stability in metallocomplexes and as ligands for certain catalytic systems.

    Comparing with Other Imidazoles—Clear Differences That Show Up in Real Production

    Clients sometimes ask why pay attention to this structural variation and not just general-purpose imidazoles. Walk the floors during a week of scale-up, and the uniqueness becomes obvious. Traditional imidazole, with only basic hydrogen substituents, interacts with acids and bases in a broad spectrum, sometimes too broadly. Chemical engineers see side reactions spike. In contrast, the methyl and phenyl substitutions restrict troublesome tautomerization and reduce by-product formation, particularly under catalytic conditions.

    Compared with 2-Phenylimidazole, which stays active in similar arenas, the methyl addition increases hydrophobic character and tweaks solubility profiles. That matters in custom syntheses, where you want clean reactions that finish on time and leave purification streams nearly free of colored tar or mixed salts. In high-throughput pharma platforms, our customers report that this variant often permits sharper crystallization and easier separation from mother liquors.

    Other aromatic imidazoles, such as 4,5-diphenylimidazole, complicate matters by introducing extra steric strain and unpredictable folding in larger molecules. They sometimes result in tangled materials difficult to separate by ordinary recrystallization or flash chromatography. Moving back to 4-methyl-2-phenyl-1H-imidazole, the compact structure simplifies workup and lets downstream transformations scale up with less troubleshooting.

    Product Application and Handling—Lessons Learned on the Plant Floor

    This imidazole stands front and center in several busy research and production pipelines. Our partners keep finding new roles for it: as a key intermediate for heterocyclic frameworks, building blocks for high-performance pigments, and in the realm of API synthesis. The product integrates smoothly into reaction sequences creating novel antifungal, anti-inflammatory, or other bioactive molecules—its clean profile and pronounced selectivity have solved stumbling blocks in several medicinal chemistry projects.

    Material scientists in polymer and electronics segments often cite its balanced pi-system and how it allows systematic modulation of physical characteristics without compromising thermal stability. Several teams use it to tailor ligand environments for late-transition metal complexes, giving catalysts longer lives and sharper conversion rates in specialty organic processes. Electrochemical applications appreciate that the product doesn’t introduce conductive variability or spurious redox activity, which proves especially advantageous in sensor prototypes and compact device coatings.

    In actual production, personnel have learned to transfer the material with air management protocols, since inhalation remains a risk during scale-up or transfer. Strict labeling and segregated storage, plus swift packaging after final drying, have reduced incidents with cross-contamination or mix-ups. Direct solvent dissolution before metering into reactors leads to uniform dispersion, and in our plant, systematic temperature ramping during addition lowers the chance of local overheating.

    Supporting Project Work with Real-World Sourcing

    One hurdle with heterocycles is always sourcing and procurement. Some buyers want just enough for an assay, others need hundreds of kilograms monthly. As direct manufacturers, we craft production schedules around these cycles, adjusting batch sizes without compromising on analytical confirmation. Feedback from long-term partners led us to invest more in packaging: inert atmosphere pouches and quick-seal drums provide practical advantages for multi-shift operations and longer-term storage.

    Technology transfer between pilot and full production is less painful because the molecule’s thermal and chemical resilience reduces cleaning cycles, waste streams, and equipment downtime. Traceability, from raw starting materials to final lot, gets tracked in our plant management software, but the most crucial insights still stem from monthly roundtables and direct calls with downstream engineers: questions about reactivity, compatibility with custom solvents, or fit with specific reactors drive our continuous improvement.

    Why Purity Levels Matter—Beyond the Catalog Values

    Standard reference sheets may list purity as a checkbox, but stories from clients, especially those scaling medical and device products, show how dealing with lower-grade imidazoles leads to recurring problems: slow color formation in stored solutions, filtration breakdowns, and even glassware etching at the trace contaminant level. Rigorous post-synthesis purifications, repeated vacuum drying steps, and ongoing communication between synthesis teams and QC analysts define this product line in our experience. Even a 0.2% difference in chlorinated impurity makes the distinction between a successful project and a month of troubleshooting in downstream columns.

    Customers developing new synthetic routes value direct access to technical support. Our chemists can walk through observed batch-to-batch shifts, relying on product logs and real-time quality data. Many have shared that troubleshooting speeds up because details aren’t hidden behind layers of traders or resellers.

    Environmental and Safety Priorities in Manufacturing and Supply

    Current expectations go beyond “is the product pure” toward building trust and safety throughout the supply chain. On the production line, our crews handle solvents and mother liquors with full vapor capture and recycling systems, not just to avoid regulatory snags but to lower the plant’s overall environmental footprint. Chemical safety officers routinely update training, so proper PPE and vented workstations remain nonnegotiable.

    Waste streams arising from the synthesis go straight to neutralization and phase separation. Once in a while, we encounter a sample batch that doesn’t meet release criteria; those never reach clients, but instead get reprocessed or disposed following a closed-loop protocol developed with environmental specialists. Documentation always runs with the product, and buyers purchasing for regulated industries can request supporting test certificates and trace records.

    Too often, supply fluctuations in raw materials hit smaller manufacturers hard. Our integrated process development keeps multiple back up suppliers in play, with regular audits and joint technical reviews. This isn’t just paperwork: minor residues from precursor variations have, in the past, caused shelf life variability and altered melting points. Addressing this at the source keeps our imidazole on track and delays at a minimum.

    Supporting Customer Innovation—A Two-Way Street

    The real test for an intermediate like 4-Methyl-2-Phenyl-1H-Imidazole comes from how readily project partners can adapt it into evolving project demands. Device laboratories might alter requirements midstream as new assay results emerge. Pharmaceutical teams run parallel synthesis programs, adjusting substituents and dosages on the fly.

    Chemists on our end sometimes collaborate directly on practical pilot demonstrations, tweaking feed solvents or temperature ramps in joint test runs. That hands-on feedback repeatedly drives changes in packaging size, anti-static lining, or even batch lot organization. Just as often, the technical conversations lead to tweaks in analytical methodology—a new NMR comparison, tighter HPLC window, or additional chiral purity report. We respond by expanding our lab SOPs and archiving method validation so repeated customizations don’t slow down future deliveries.

    Real-world formulation teams often flag performance issues only after integrating intermediates into target products, such as gradual discoloration under accelerated aging, or solubility drift in certain carriers. Our own R&D group acts as a listening post. Often, lab-scale investigations kicked off by these customer discoveries have pointed toward subtle process impurities or drying parameters that could use tuning. We rework batch routines and involve production leadership on both sides, so troubleshooting never stops at a written recommendation.

    Conclusion: Trusted Supply Based on Direct Experience

    Supplying high-purity 4-Methyl-2-Phenyl-1H-Imidazole isn’t just a matter of shipping an item off the shelf. Long exposure to production, screening, and close technical support forged a product that fits both cutting-edge and routine applications. The chemical manufacturing community benefits from consistent engagement, product transparency, and a commitment to quality at every stage. As project demands shift and end uses expand, customers can count on our insight brewed from years at the bench and decades on the plant floor.