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4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid

    • Product Name 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid
    • Alias Telmisartan
    • Einecs 613-199-0
    • 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

    697212

    Chemical Name 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid
    Cas Number 109295-35-4
    Molecular Formula C12H14N2O2
    Molecular Weight 218.25 g/mol
    Appearance White to off-white solid
    Melting Point 220-224°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Smiles CCCN1C2=C(C=C(C=C2)C(=O)O)N=C1C

    As an accredited 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 25 grams of 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid, labeled with chemical name, batch number, and hazard information.
    Shipping 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It should be handled with care as a laboratory chemical, conforming to all relevant regulations for transport of chemicals. Appropriate documentation and hazard labeling accompany the package to ensure safe, compliant delivery.
    Storage 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and store at room temperature unless otherwise specified by the manufacturer or safety data sheet.
    Application of 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid

    Applications of 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid in Industrial Manufacturing

    4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid serves as a high-purity intermediate widely adopted in the pharmaceutical sector, especially in the development of certain antihypertensive drugs and active pharmaceutical ingredients (APIs). Its demanding synthesis controls and precise formulation requirements determine specialized adoption by manufacturers pursuing advanced small-molecule therapeutics and related fine chemicals. Below, we outline key application scenarios reflecting actual downstream industrial practices and compliance frameworks.

    1. Angiotensin II Receptor Blocker (ARB) API Synthesis

    This benzimidazole derivative is essential in the multi-step synthesis of sartans, a major class of ARB antihypertensive agents. Its incorporation enables selective modifications and ring closure steps integral to structure-activity tuning in active drug substances. Downstream API plants employ strict release and in-process QC, given the direct path from raw material to regulated pharmaceutical intermediates and end products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP, Ph. Eur., JP monographs for ARB APIs (e.g., Valsartan, Irbesartan)
    • 21 CFR Part 211 (US cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia standards for hypertensive drugs

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents per designated intermediate step, with slight adjustment for route-specific yields and impurity profiles

    Downstream process integration

    • Introduced during amidation and cyclization phase post-initial aliphatic alkylation and pre-final deprotection stages
    • Reacted under anhydrous conditions with controlled temperature ramp and nitrogen purge

    Final product types

    • Pharmaceutical-grade ARB APIs including Valsartan, Irbesartan, and related benzimidazole-based drug substances

    2. Active Intermediate for Custom Synthesis in CDMO/CMO Services

    Contract manufacturers specializing in custom chemical synthesis integrate this benzimidazole acid during rapid route scouting for new chemical entities (NCEs) and intermediate building blocks. The material’s reactivity profile supports iterative structure modification and scale-up campaigns where clients require route flexibility and robust impurity tracking prior to moving into GMP clinical manufacturing.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • SafeBridge Potent Compound Handling Certification (when handling HPAPIs in later steps)
    • Client-specific impurity and residual solvent limits based on ICH Q3A/Q3C
    • EHS compliance for laboratory and pilot facilities (REACH registration in the EU, US OSHA standards)

    Typical usage ratio

    • Adopted at 0.5–1.4 molar equivalents depending on target NCE structure and number of steps required for convergence

    Downstream process integration

    • Fed as a late-stage intermediate after core scaffold assembly to enable functional group diversification or side-chain introduction
    • Subjected to strict batchwise in-process checks for isomer ratio and residuals

    Final product types

    • Pharmaceutical research intermediates for clinical candidates
    • Chemical building blocks for proprietary NCE libraries

    3. Fine Chemical Intermediate for Advanced Organic Synthesis

    Producers of specialty benzimidazole derivatives and heterocyclic compounds utilize this acid in routes involving regioselective transformations and elaboration to high-value ligands and custom complex molecules. These materials often serve as the foundation for exploring new pharmaceutical leads or catalytic ligands for process development, tested under rigorous purity and analytical standards to meet client specifications in advanced R&D pipelines.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • REACH (EU) compliance for registration of custom-made intermediates
    • GHS/CLP labeling and safety documentation for transport and laboratory use
    • RoHS (as applicable for electronic/catalyst precursors)

    Typical usage ratio

    • Between 1.0–2.0 equivalents per target molecule, with quantity driven by intended functional group density and desired degree of substitution

    Downstream process integration

    • Used as a pre-cursor for further ring closure, amide bond formation, or selective alkylation reactions in multi-step fine chemical synthesis
    • Subject to intermediate purification, often via column chromatography or crystallization

    Final product types

    • Research-grade benzimidazole derivatives for drug discovery
    • Custom heterocyclic compounds for process development and scale-up evaluation

    4. Reference Standard Material Sourcing for Analytical Laboratories

    Analytical reference standard providers source this compound at ultrapure grades for use in calibration, assay validation, and method development for pharmaceutical and regulatory laboratories. The integrity of such reference batches allows QC teams in downstream plants to confirm method accuracy during impurity profiling and batch release for regulated finished pharmaceutical products containing benzimidazole structures.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory quality management and competence
    • FDA/EMA guidance on reference standard qualification
    • USP General Chapter <823> (Radiopharmaceuticals – Analytical Methods, where applicable)
    • GMP documentation and chain-of-custody controls

    Typical usage ratio

    • Utilized as a reference at quantities from 1–50 mg per analytical run, depending on method sensitivity and validation batch size

    Downstream process integration

    • Supplied for direct use in HPLC, GC, or LC-MS calibration and quantitation workflows during QC of ARB APIs and finished dosage forms
    • Prepared under strict documentation and batch traceability protocols

    Final product types

    • Certified analytical standards for pharmaceutical QC labs
    • Reference solutions for regulatory submission dossiers and stability studies
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    Certification & Compliance
    More Introduction

    Introducing 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid: Precision and Reliability from Our Factory Floor

    Purpose Built for Advanced Synthesis

    Stepping into the specialty chemicals segment, we have spent years refining our process for 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid, a core benzimidazole intermediate. This compound, with its methyl and N-propyl substitutions, unlocks unique reactivity in pharmaceutical synthesis, serving as a proven scaffold for advanced molecules. Each production batch owes its consistency to our hands-on experience and the direct control we maintain from raw input to finished, packaged product.

    Model and Preparation: What Sets Our Material Apart

    Manufacturing this acid is never just about hitting a purity number. Our most requested specification remains the standard crystalline form, with purity levels regularly exceeding 99 percent by HPLC. Chemists at our site monitor every step—reaction, filtration, wash, and final drying. Careful temperature regulation and slow crystallization help minimize unwanted isomers or trace impurities.

    Every drum leaving our facility comes accompanied by full analysis data: NMR, mass spectrometry, and moisture content below 0.5%, as confirmed by Karl Fischer titration. Process adjustments—sometimes minor shifts in solvent or reaction time—make the difference between routine output and a grade usable for both R&D and demanding commercial supply.

    Why 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid Matters in Modern Chemistry

    From our work with customers and in-house teams, this benzimidazole carboxylic acid finds greatest use as a building block in pharmaceutical and agrochemical pipelines. The specific methyl and propyl substitutions help to modulate biological activity and metabolic stability in target molecules. Compared to simpler benzimidazole carboxylic acids, which may lack the desired reactivity or selectivity, this compound introduces a valuable degree of chemical tunability.

    Project chemists routinely share their struggles with side reactions using less substituted benzimidazole derivatives. Through process optimization, we've cut down on contaminant peaks that can complicate downstream purification—a direct result of improved purification steps and the unwillingness to accept off-spec production. Controlled reactivity allows medicinal chemists to introduce further modifications without protective group gymnastics, saving both time and budget in early-stage discovery and scale up.

    Consistency and Traceability—From Raw Material to Finished Acid

    Over years of working closely with procurement teams and process engineers, we've recognized recurring pain points: unpredictable quality, supply interruptions, and gaps in analytical documentation. We address these immediately, starting by sourcing starting materials via established, vetted suppliers only. Each shipment receives full traceability documentation and a log of batch records accessible for regular audits.

    Unlike outfits that act as intermediaries or trade through opaque channels, our manufacturing and analytical team supports every stage, from kilo lab validations to full-scale drum shipments. This has earned the trust of synthetic route developers who demand assurance not just in theory, but in measurable, repeatable results every time material arrives at their dock.

    Meeting Evolving Standards and Customer Expectations

    The regulatory climate for pharmaceutical precursors continues to tighten, especially for benzimidazole derivatives as more end uses reach the market. Our teams work directly with compliance teams to ensure every document meets the needs of quality assurance officers, and proactively monitor changes in requirements. Customers in both the EU and North America have shared that advanced documentation—certainly a step up from generic commodity materials—often speeds up their own internal qualification steps.

    We run periodic impurity studies and hand over full impurity profiles alongside standard COA. This transparency has helped several international partners avoid last-minute delays in API project timelines, otherwise slowed down by missing or incomplete impurity declarations from offshore sources. The reliability of final product identity directly supports patent filings and regulatory submissions, a topic on which our technical team regularly consults with client process engineers.

    Usage Scenarios—Supporting the Innovation Pipeline

    We regularly supply both multigram lab-scale orders and large, full-pallet lots. Medchem groups often source small batches for lead optimization, leveraging the enhanced substitution pattern for SAR (Structure Activity Relationship) studies. At process scale, customers in commercial API production favor our material for its predictable yield and reduced side product formation, translating into faster clinical and preclinical batch progression.

    Agrochemical developers recognize potential advantages in metabolic pathways, where even a small change in substitution leads to a significant improvement in biological profile or shelf life. The same tightly controlled process parameters making our pharmaceutical clients return for repeat orders benefit agrochemical and specialty intermediate clients, ensuring that pilot plant findings scale up without performance surprises.

    Reducing Uncertainty in Custom Synthesis

    We have witnessed projects get derailed due to inconsistent upstream materials—side reactions triggered by low-level metal ions or unexpected polymorphs. To counter this, we've invested in line-dedicated reactors and controlled atmosphere sampling for air-sensitive batches, which means no cross contamination and greater confidence in batch-to-batch comparability.

    Long-standing customers often visit to audit our site, gaining direct familiarity with our QA processes. More than one has remarked on the difference they find compared to resellers: direct sampling, on-the-spot analytical checks, and a willingness to discuss not just finished specs but what decisions led to process changes at the plant level.

    Comparing 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid To Close Structural Relatives

    Over years of application support, our team has compared this compound to both basic benzimidazole derivatives and structurally related carboxylic acids. The propyl and methyl groups clearly alter pharmacokinetics and often yield more targeted binding affinities in certain biological assays. Customers report reduced volatility and lower residue on ignition compared to unalkylated acids, which can matter in pilot-scale API synthesis.

    In side-by-side process trials, our product has shown lower impurity drift across multiple batches compared to bulk sources of other benzimidazoles. Such consistency depends not only on careful synthetic control, but also tight adherence to drying, storage, and packaging requirements—our team tracks every process variable across each lot, providing a full report with every shipment.

    Supporting Customers Beyond Supply

    Our chemical engineers regularly consult with formulation scientists and process development teams exploring custom derivatives. In some projects, the slightly larger molecular footprint of our acid unlocks a new functional handle for selective coupling reactions, reducing the number of steps to final product. We maintain active collaboration agreements with institutions for method development, sharing analytical protocols and quality benchmarks freely.

    Supply support means more than a certificate of analysis. Our site operations stay flexible to accommodate tight deadlines, off-cycle delivery windows, and emergency re-supply, even during volatile market conditions for key starting materials. This level of support draws on a decade of learning what pharma and fine chemical teams value most: direct access, no minimum order surprises, and quick transparency on any issue that emerges in process or analysis.

    Continuous Improvement and Long-Term Relationships

    Every feedback call and deviation report teaches us something new. Operators in our reactors log even minor fluctuations in temperature or solvent quality, feeding real-world data into our routine continuous improvement cycles. Recent investments in automated sampling allow us to catch trace impurities faster, with less reliance on off-line batch analysis and more on in-line monitoring.

    Customers returning for repeat business often mention the value of being heard—suggesting tweaks to drying cycles, storage packaging tailored to their stability requirements, and batch splitting to minimize exposure. Instead of resting on standard protocols, we adapt with the needs of chemists at the bench and the plant. Such flexibility, built up through years of direct engagement, helps us predict process pain points and reduce scale-up headaches before they reach the customer.

    Facing Market Challenges with Experience

    The market for benzimidazole intermediates shows cycles of tightness—raw material spikes, transport disruptions, changing regulatory classifications. Experience tells us that keeping a buffer stock of critical reagents and investing in alternate sourcing pays off when global events hit the supply chain. Contingency plans extend to backup utilities, dual-qualified analytical methods, and a reserve of well-trained operators ready to run extra shifts.

    We have seen demand surge in some years with next-generation molecules moving through clinical pipelines. This makes consistent production scale and predictable supply ever more important. Our site maintains redundancy in key equipment and qualifies secondary routes to maintain continuous operation, supporting both steady and surge requirements.

    Differences That Come From Manufacturer Direct Commitment

    While others may aggregate materials from multiple origins, we stand by the principle that factory-direct supply remains the surest way to guarantee both quality and reliability. Differences emerge not only in the metrics—a narrower melting range, tighter residual solvent levels, robust trace metals control—but also in the confidence this brings to every process development milestone our customers aim to hit.

    Collaborating directly with leading research groups, we gather application data that shapes our own process development, closing the loop between lab discovery and plant-scale reliability. Requests for new packaging formats, rush delivery, or non-standard analytical documentation receive prompt action because the decision makers are never more than a few steps from the shop floor.

    Upholding Trust Through Transparency

    Every finished batch of 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid carries with it the story of operator expertise, direct process monitoring, and the lessons learned from dozens of customer campaigns. We believe that trust comes not from a brand, but from the steady delivery of honest information and solutions tailored to specific synthesis challenges.

    Customers new to our material often ask for pilot batch samples, site audits, and in-depth technical Q&A, reflecting today’s expectations for transparency and engagement. We embrace these requests, sharpening our systems to meet this ever-higher bar, and proactively updating technical files as analytical standards or compliance needs evolve.

    The Manufacturer’s Perspective: What Direct Control Means for Innovation

    Years in specialty manufacturing have drilled in the truth that delivering a pure compound is only part of the story. Supporting projects from first evaluation through to commercial rollout calls for readiness: resolving unexpected side reactions, offering tailored drying or grind sizes, and sharing insights on shelf stability and handling. Direct engagement with working chemists highlights small changes with big impact—switching the vessel lining, nudging a reaction exotherm, or introducing closed nitrogen handling for air-sensitive projects.

    We document each adaptation and feed improvements back into routine production, always with a view on how downstream users will face less troubleshooting. Close collaboration with leading formulators has shown that this particular substituted benzimidazole offers both synthetic flexibility and performance upside, and its ready adaptation to custom derivatization opens new avenues that simpler scaffolds cannot easily match.

    Looking Ahead: Continuous Innovation Backed by Experience

    We have seen the specialty chemicals sector shift rapidly, with higher scrutiny on both process and product. Meeting quality commitments while supporting breakthroughs in pharma and agrochemicals brings out the ingenuity in both our chemistry and our operations teams. Experience tells us shortcuts in control or documentation never pay off—only thoroughness wins.

    The ongoing dialogue with our partners, both new and long-established, shapes our focus every year. Market trends, tighter specs, and new project types drive us to keep learning, refining, and adapting. In every drum of 4-Methyl-2-N-Propyl-1H-Benzimidazole-6-Carboxylic Acid that leaves our plant, we aim to deliver the quiet assurance that comes from direct manufacturer commitment, rigorous process control, and plainspoken support for every customer’s success.