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

4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole

    • Product Name 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole
    • Alias BTPB
    • Einecs 629-767-8
    • 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

    300634

    Chemical Name 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole
    Molecular Formula C11H9BrF3N2O
    Molecular Weight 339.11 g/mol
    Cas Number NA
    Appearance White to off-white solid
    Solubility Soluble in DMSO, methanol
    Purity Typically >98% (HPLC)
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms No widely recognized synonyms
    Smiles CC(CO)Nc1nc2ccc(Br)cc2nc1C(F)(F)F
    Iupac Name 4-Bromo-2-(3-hydroxypropyl)-6-(trifluoromethyl)-1H-benzimidazole

    As an accredited 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White polyethylene bottle containing 25 grams of 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole, securely sealed with tamper-evident cap.
    Shipping This chemical, **4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole**, is shipped in tightly sealed containers, protected from moisture and light. It is packaged according to applicable hazardous material regulations, including UN-rated packaging if required. Shipment occurs via certified carriers with proper labeling and accompanying Safety Data Sheets (SDS) to ensure regulatory compliance and safe handling during transit.
    Storage 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole should be stored in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerated). Store in a well-ventilated, cool, dry area away from incompatible substances such as strong oxidizing agents. Proper labeling and secondary containment are recommended to prevent accidental release or contamination. Handle under a chemical fume hood if possible.
    Application of 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole

    Applications of 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole in Industrial Manufacturing

    As the original manufacturer of 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole, we supply this intermediate to a limited range of highly specialized industries that rely on its advanced chemical properties. The information below details authentic downstream industrial application environments, with each section developed from technical feedback and regulatory standards in actual use. This section is designed for technical teams, industrial procurement, and process engineers seeking validated application pathways.

    1. Pharmaceutical Intermediates for Antiviral API Synthesis

    Major pharmaceutical API manufacturers use this compound as a key intermediate in the synthesis of select benzimidazole-based antivirals targeting RNA viruses. It enters the synthetic route at a defined functionalization stage requiring both trifluoromethyl and bromine substituents to develop specific pharmacophores. Its application is directly referenced in DMFs (Drug Master Files) for regulated markets, with batch traceability and impurity profile control integrated harmoniously into multi-step GMP synthesis workflows.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4, Annex 2 for APIs
    • Relevant method validation protocols (USP, Ph. Eur.) for residual analysis

    Typical usage ratio

    • Employed at 0.8%–2.5% molar equivalent in specific stage reactions, adjusted according to target API route and scale of batch to ensure optimal yield without excess residual impurity

    Downstream process integration

    • Added as a core reactant following primary aromatic ring assembly, participates in nucleophilic substitution or alkylation steps under inert conditions, fully converted before chromatographic or crystallization purification

    Final product types

    • Antiviral active pharmaceutical ingredients (APIs) for human medicinal products
    • Research-grade antiviral intermediates
    • Registered pharmaceutical substances under market authorization

    2. Specialty Chemical Synthesis for Agrochemical Intermediates

    Manufacturers in the agrochemical sector use this compound as a strategic intermediate for producing benzimidazole-structured pre-products, later processed into fungicidal or pest-resistance agents. Its defined halogen and hydroxylpropyl groups facilitate further derivatization, crucial for fine-tuning bioactivity profiles specific to modern crop protection requirements. Quality assurance teams emphasize both trace-level impurity monitoring and known synthetic pathway reproducibility.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacture
    • FAO/WHO JMPR guidelines on pesticide specifications
    • REACH (EC) No 1907/2006 for substance registration and notification
    • CROP-LIFE International guidelines for supply chain traceability

    Typical usage ratio

    • Utilized at 1.2%–3.0% of total active intermediate batch weight, with process chemists adjusting based on downstream derivatization needs and target efficacy benchmarks

    Downstream process integration

    • Dosed at the benzimidazole intermediate assembly stage, frequently under controlled temperature and pH to safeguard halogen functional integrity prior to subsequent side-chain introduction or protection/deprotection sequences

    Final product types

    • Precursor compounds for broad-spectrum fungicides
    • Herbicide intermediates containing modified benzimidazole cores
    • Agrochemical screening libraries for R&D field trials

    3. Fluorinated Building Blocks in Advanced Material Science

    Producers of advanced specialty polymers and fluorinated materials incorporate this compound as a building block to introduce both high electron-withdrawing capability and targeted reactivity via its trifluoromethyl and benzimidazole motifs. The material exhibits high performance in modifying polymers used for coatings and electronic encapsulation, with precise stoichiometry governed by molecular weight targets and resin specifications.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System (required for fluorochemicals)
    • RoHS Directive 2011/65/EU (Restriction on Hazardous Substances in Electronics)
    • REACH compliance for monomeric and polymeric raw inputs
    • OEM-specific incoming material specifications (Japanese JIS, US ASTM D standards)

    Typical usage ratio

    • Integrated at 0.2%–0.9% by weight of total polymer mass, adjusted based on target fluorine loading and mechanical property requirements

    Downstream process integration

    • Introduced in pre-polymerization stage via solution blending or co-polymerization; reactivity profile dictates single-reactor use for streamlined encapsulation or two-stage processes for specialty resins

    Final product types

    • High-performance fluorinated polymers for coatings and adhesives
    • Encapsulation materials for microelectronics
    • Research-grade polymer blocks with custom benzimidazole fluorine motifs

    4. Specialty Dye and Pigment Intermediate

    Leading dye and pigment manufacturers utilize this benzimidazole derivative for generating specialty pigments with targeted brilliance and stability, particularly those demanding trifluoromethyl-induced chromophore shifts and bromine-mediated reactivity to support substituted dye frameworks. Strict analytical protocols track the transformation efficiency and chromogenic strength, allowing producers to deliver advanced-grade colorants to the textile and plastics sectors.

    Industry compliance standards

    • Oeko-Tex Standard 100 (safety assessment for textiles)
    • EN 71-3 (European safety standard for toy colorants)
    • ISO 9001:2015 Colorant Manufacturing requirements
    • Chemical Substance Control Law (CSCL, Japan) for pigment regulatory reporting

    Typical usage ratio

    • Used at 0.6%–2.1% of total dye formulation mass, with the exact amount fine-tuned against required color fastness, stability, and hue intensity across different pigment types

    Downstream process integration

    • Enters the diazotization or condensation stage of azo and benzimidazole dye synthesis, often reacted under solvent reflux and monitored via real-time HPLC to optimize colorant yield

    Final product types

    • High-stability textile dyes
    • Plastic colorants for industrial polymers
    • Special effect pigments for coatings and inks
    Free Quote

    Competitive 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole 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

    Introducing 4-Bromo-2-(3-Hydroxypropyl)-6-(Trifluoromethyl)Benzimidazole

    Product Experience from the Manufacturing Floor

    In our years of synthesizing specialty benzimidazoles, 4-Bromo-2-(3-Hydroxypropyl)-6-(trifluoromethyl)benzimidazole has taken up a unique corner of our production line. Labs searching for functional diversity in their benzimidazole intermediates often arrive at this material for its specific balance of reactivity and compatibility. Many researchers know how challenging it can be to build molecules that cooperate with modern catalytic and protecting group strategies. We have refined our process so each lot carries consistent purity and functional group presentation, which remains essential for reaction reliability in downstream applications.

    Structural Features that Matter in Practice

    Our teams work closely with both medicinal chemists and materials scientists striving for molecular inventiveness. This compound’s hallmark feature—the 3-hydroxypropyl substituent at position 2—offers hydrophilicity not often seen in halogenated benzimidazoles. That group improves solubility and broadens physical processing options. The bromine at position 4 presents valuable versatility for coupling reactions, especially Suzuki and Buchwald-Hartwig aminations, because the electron-withdrawing trifluoromethyl at position 6 tempers its reactivity just enough for controlled stepwise coupling. While some benzimidazoles behave unpredictably under cross-coupling, ours withstand repeated exposures to bases and transition metals, thanks to a process that removes troublesome trace metals and residual halides.

    Commitment to Chemical Integrity

    Consistency in product quality can only be achieved through relentless attention to detail. In this industry, shortcuts rapidly breed inconsistencies in analytical profiles, leaving chemists frustrated when impurities creep through purification steps. Our production avoids batch-to-batch variation by relying on high-purity raw materials and validated step-wise syntheses. Each time our process scales up, we review every analytical trace to confirm that the hydroxypropyl group’s integrity remains intact—a step critical for downstream derivatization. Rigorous HPLC and NMR analyses back every shipment.

    Real-World Usage and Value

    4-Bromo-2-(3-Hydroxypropyl)-6-(trifluoromethyl)benzimidazole has demonstrated its worth both in early drug candidate screening and advanced material projects. Pharmaceutical researchers use it as a pharmacophore scaffold where the trifluoromethyl group boosts metabolic stability and oral bioavailability. The bromine frequently acts as a selective coupling handle for late-stage diversification, giving development chemists precise control over downstream functionalization. These groups do not simply exist in theory—they bring genuine experimental flexibility that directly impacts lead optimization.

    In one project, a customer’s team leveraged the hydroxypropyl side chain to introduce water solubility into derivatives that previously posed formulation headaches. Small changes in molecular property can sometimes solve complex bottlenecks, and multiple partners have told us that our controlled manufacturing has minimized surprises at the purification bench. Not all benzimidazole intermediates support high-throughput chemistry; ours responds predictably in microwell combinatorial syntheses, surviving vigorous reagents and temperature ramps without decomposition or rearrangement.

    Reliability Sets Us Apart

    We do not approach benzimidazole production as mere assembly. We recognize how much each research project stakes on consistency, so our workflow prioritizes lot uniformity from kilogram scale on up. Some alternatives on the market arrive with yellowish tints or odd particulate contaminants—almost always a symptom of incomplete crystallization, residual solvent, or starting material breakdown. We avoid these pitfalls by optimizing every step, including recrystallization and vacuum drying, to yield a free-flowing solid that behaves consistently in analytical and preparative settings.

    Analytical reproducibility is not a marketing pitch, it’s an expectation that enables real progress for synthetic chemists. On several occasions we’ve received feedback that our material’s narrow melting point range offers reliability during reaction setup, so time lost on failed scale-up reactions drops sharply. Laboratories developing regulated materials benefit from our robust characterization, which minimizes disruptions from ambiguous impurity peaks or drifting purity percentages.

    Process Insights and Technical Innovations

    Experience with electron-rich and electron-poor benzimidazole chemistry gives us an understanding of how critical product purity is. Residual inorganic salts pose risks in cross-coupling chemistry by poisoning catalysts or causing precipitation in flow systems. Through repeated optimization cycles, we designed a workup sequence that strips away metallic and organic contaminants, so each batch outperforms typical purity benchmarks in side-by-side analyses. Earlier generations of this molecule often carried sub-visible residues from bromination or alkylation steps, frequently frustrating downstream colleagues tasked with scale-up or formulation. Systematic improvements—such as phased solvent exchanges and temperature controls—now eliminate those concerns without sacrificing yield.

    We’ve partnered with universities troubleshooting problematic reaction routes, and that experience highlights just how varied lab conditions can be. Some groups require finer particle sizes for automation platforms, while others prefer bulk crystalline form for milligram-to-gram preparations. Our line supports both preferences with robust crystallization protocols and adaptable grinding mills, meaning material transitions smoothly from bench discovery to late-stage synthesis.

    Continuous Feedback and Transparent Improvement

    Manufacturing specialty benzimidazoles involves a conversation with those on the receiving end—scientists and engineers with few minutes to waste trouble-shooting unreliable precursors. We actively solicit raw feedback from customers, chemical development teams, quality control laboratories, even formulation experts working at multinational pharma and materials plants. Several recommendations from these partners have led to new QC checks, such as expanded impurity fingerprinting and tighter water-content specs. With each improvement, we cycle back upstream, recalibrating reactors and changing handling procedures based on real use case data, not speculation.

    Direct experience reveals pain points that generic data sheets rarely capture. One group requested tighter control over the hydroxypropyl group’s enantiomeric purity for potential chiral resolution projects. This led our in-house chemists to collaborate with asymmetric synthesis specialists, tightening process design and chiral chromatography checks. Not every request results in a new product line, but our adaptability ensures the core benzimidazole remains ready for evolving application demands.

    Comparing Structure and Performance with Related Products

    The differences from conventional benzimidazoles go beyond an extra halogen or alkyl chain. Some analogues, such as 4-bromo-6-trifluoromethyl benzimidazole lacking the hydroxypropyl group, show lower aqueous dispersibility, narrowing their application to less challenging formulations. We notice that our product, with its balance of hydrophobic and hydrophilic groups, performs well in pharmaceutical salt formation as well as organic electronics precursor work.

    Without the 3-hydroxypropyl side chain, related derivatives often fall short in solution-based processes, sometimes causing precipitation or emulsification issues that disrupt scale-up work. By deliberately adding this moiety, our product can participate in hydrogen bonding and offer new points for functionalization, so synthetic chemists unlock more inventive routes. This structure also avoids the excessive lipophilicity that complicates absorption modeling and makes analogues more stubborn in formulation.

    Supporting a Changing Research Landscape

    Research priorities in both pharma and specialty materials continue shifting towards molecules with “tunable” reactivity and multi-functional handles. Our approach couples the speed of industrial-scale synthesis with a focus on customization. No two research pipelines need exactly the same benzimidazole intermediate—so we build flexibility not just into our catalog, but into the heart of our production train. Project timelines shrink and scale-up teams waste less effort, because our product is intended for direct synthetic use with minimal preconditioning.

    In real-world settings, some intermediates look nearly identical on paper but depart drastically in practice. A batch with high residual halide may destabilize a palladium catalyst, or a formulation with over-dried powder could clump in automated feeders. Our chemists constantly review each synthetic lot for small shifts—color, texture, melting point—to ensure material reaches customers in a condition that “just works.” Sourcing from a manufacturer who understands reaction mechanisms and follows each lot to conclusion saves teams months of debugging time.

    Environmental Responsibility and Safe Handling

    Our work comes with responsibility. We dedicate significant resources to waste minimization, solvent recycling, and energy-efficient reactions. The synthetic routes chosen avoid persistent halogenated byproducts and limit hazardous side streams whenever possible. Proper handling practices are critical, but our packaging, quality controls, and robust documentation allow teams to focus on discovery, not troubleshooting mysterious impurities or shipment surprises.

    We keep the conversation about sustainability open, inviting reviewers and regulatory teams to audit both process and product. Waste streams receive documented attention through on-site pretreatment and certified off-site disposal partners. Regular training updates across production, R&D, and packaging teams reflect both global industry expectations and lessons learned from those using our compounds on the lab bench.

    Experience Shapes Better Bench Chemistry

    Lessons build from every lot shipped, lesson learned, and partner collaboration. We see the way a material’s predictability, even more than its price or available documentation, determines how quickly a research team can move from concept to publishable data. That is why the path to innovation remains so closely linked to having reliable, well-characterized starting points. We back each shipment with documentation including HPLC, NMR, and relevant trace metal studies, since informed researchers want more than surface-level information.

    Support does not end at shipment. Our technical team remains available for practical discussion, troubleshooting, and laboratory insight. We share updates as advances in asymmetric synthesis, process intensification, or new regulatory trends impact either our processes or the utility of benzimidazole intermediates broadly. Many of those improvements—better crystal forms, improved washing protocols, reduced environmental footprints—trace back to the original insights or complaints of end-users.

    No Substitute for Manufacturing Experience

    Working daily with benzimidazoles means we discover the small details others ignore. Attention to mechanical handling, fully dried powders, batch-to-batch color consistency, and fine-tuned melting points distinguish our offering from generic catalogues and commodity traders. Working directly with the people who purchase and use these chemicals, and adjusting our manufacturing based on actionable feedback, lets both parties avoid unnecessary delays, failures, and added costs.

    In the end, what sets 4-Bromo-2-(3-Hydroxypropyl)-6-(trifluoromethyl)benzimidazole apart isn’t just smart functionalization or an attractive product number. It is the sum of process experience, technical care, and thousands of grams tested under many real-world conditions. Each batch represents a conversation—between our expert chemists, the machines and molecules they guide, and the users who depend on reliability every step of the way.