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2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride

    • Product Name 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride
    • Alias HNMT Inhibitor 15
    • Einecs 611-668-3
    • 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
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    Specifications

    HS Code

    941612

    Product Name 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride
    Chemical Formula C11H14N2 · HCl
    Molecular Weight 210.71 g/mol
    Appearance White to off-white solid
    Cas Number 23056-32-0
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Solubility Soluble in water and polar organic solvents
    Melting Point 180-183°C (decomposition)
    Synonyms 1-(2,3,4,4a-Tetrahydronaphthalen-1-yl)imidazoline hydrochloride
    Category Imidazoline derivative
    Application Pharmaceutical intermediate, research chemical

    As an accredited 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 10-gram amber glass bottle, sealed, labeled with "2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride, 10g, for research use only."
    Shipping 2-Tetralin-1-yl-4,5-dihydro-1H-imidazole hydrochloride is shipped in tightly sealed containers, protected from light and moisture. It is packed according to regulatory requirements for handling chemicals, with appropriate hazard labeling. Temperature-sensitive shipping methods may be used if necessary, ensuring safe delivery without degradation of the compound.
    Storage Store **2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride** in a tightly sealed container, protected from light and moisture. Keep at room temperature (15-25°C) in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Ensure storage is secure and clearly labeled, and limit access to trained personnel. Follow all applicable chemical storage regulations.
    Application of 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride

    Applications of 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride in Industrial Manufacturing

    Our manufacturing facility delivers 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride in commercial volumes to support critical synthesis processes across multiple industrial sectors. We focus on direct input for downstream industries where this compound plays a functional, value-adding role in specialty production. Below we outline key application scenarios, including compliance expectations, precise incorporation strategies, technical process integration, and representative finished product categories.

    1. Pharmaceutical Intermediate for Antihypertensive Drug Synthesis

    Pharmaceutical manufacturers use this ingredient as a building block in multi-step synthesis routes for specific antihypertensive agents, particularly imidazoline-based receptor modulators. In active pharmaceutical ingredient (API) manufacture, it serves as a key intermediate subjected to defined GMP and quality standards, playing a role in amine condensation or cyclization stages prior to the final purification of the drug substance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • Pharmacopoeial requirements (USP, Ph. Eur.) for process intermediates
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • EU Directive 2001/83/EC on medicinal product manufacturing

    Typical usage ratio

    • Employ 0.8–1.2 molar equivalents per target molecule in intermediate stages. Adjustments depend on reaction scale and process yield controls determined by in-process sampling and impurity profile monitoring.

    Downstream process integration

    • Input during reductive amination or cyclization steps in multi-step syntheses; batch-fed into reactor vessels following solvent charging and preconditioned pH adjustment.

    Final product types

    • API crystallized forms of imidazoline-class antihypertensive drugs
    • Tablet-ready bulk drugs after purification and granulation
    • Pharmaceutical intermediates for further chemical elaboration

    2. Catalyst Precursor in Specialty Polymer Additive Manufacturing

    Chemical processing plants employ this compound as a select precursor for fine-tuned polymerization catalysts, particularly for ring-opening or living polymerizations requiring imidazole-derived systems. Application includes pilot to commercial scale production lines for engineering plastics, where polymer grade requirements demand direct precursor validation and controlled addition to masterbatch reactors.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical process industries)
    • REACH Registration (EU regulation for chemical substances)
    • OECD Guidelines for Testing of Chemicals – Polymer specifications
    • GB/T 13508-2011 (China - Polyester, Polyamide, and specialty polymer additive standards)

    Typical usage ratio

    • Utilize 0.05–0.15 wt% based on total monomer charge; adjust according to targeted polymer properties and catalyst turnover, subject to validation trials and in-plant process data log.

    Downstream process integration

    • Added during initial solution or melt blending of monomers pre-polymerization; entered under nitrogen or inert atmospheres to prevent premature catalyst deactivation.

    Final product types

    • Engineering thermoplastics (e.g., polyamides, polyesters with improved mechanical profiles)
    • High-performance copolymers for automotive and electronic applications
    • Masterbatch concentrates for additive compounding

    3. Intermediate in the Synthesis of Agrochemical Active Compounds

    Crop protection chemical producers source this intermediate for constructing nitrogen-containing heterocyclic moieties, a common motif in modern fungicide and herbicide molecules. Its usage permits modular assembly of imidazoline scaffolds via ring fusion steps. Production is typically confined to multi-purpose agrochemical synthesis plants under strict residual management controls.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001 and ISO 14001 (for quality/environmental management in agrochemical production)
    • GLP compliance – OECD Principles of Good Laboratory Practice for pesticide testing
    • EPA registration requirements (40 CFR Parts 150–189 for US agrochemicals)

    Typical usage ratio

    • Incorporate at 1.0–1.5 mole equivalents relative to target agrochemical intermediate; optimized through pilot studies for step yield and residual parent compound control.

    Downstream process integration

    • Dosed into closed reactors during heterocycle assembly; participates in condensation or selective hydrogenation operations prior to downstream functionalization.

    Final product types

    • Formulated fungicidal and herbicidal active agents
    • Granular and suspension concentrate crop protection products
    • Technical-grade intermediates for advanced synthesis

    4. Building Block for Fine Chemical Synthesis in Dye and Pigment Industries

    Dye and pigment manufacturers leverage this compound as a specialty reactant to introduce rigid, nitrogen-containing ring systems into advanced colorant molecules. In such applications, precise stoichiometric addition and stagewise reaction control ensure the required chromophore and solubility characteristics for high-performance industrial dyes destined for plastics, textiles, and coatings.

    Industry compliance standards

    • EN 71-3:2019 (European Safety Standard for toys regarding colorant chemicals)
    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) testing protocols
    • ISO 9001:2015 for procedural quality assurance in dye manufacture
    • CFR Part 1480 EPA (US Toxic Substances Control Act for colorants)

    Typical usage ratio

    • Utilize 0.2–0.9 molar ratio, calibrated according to chromophore development and pigment load; batch-to-batch variation based on end-use visibility and dispersibility testing.

    Downstream process integration

    • Incorporated in azo or anthraquinone dye syntheses via amination, ring closure or coupling reactions; integrated into early reaction stages under closed-system safety protocols.

    Final product types

    • High-stability industrial dyes for plastics and synthetic fibers
    • Disperse and reactive dyes for textile applications
    • Specialty pigments for coatings, inks, and paints

    5. Precursor in Research-Grade Chemical Development for Analytical Laboratories

    Certified chemical suppliers and analytical research institutions incorporate this raw material as a precursor for synthesizing custom reference standards, calibration solutions, and molecular probes. Such usage responds to demands for analytical-grade purity and trace impurity characterization, particularly in the context of developing detection kits or validating instrument performance across regulated fields.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing and Calibration Laboratory Accreditation)
    • American Chemical Society (ACS) Grade Reagent protocols
    • Good Laboratory Practice (GLP) for reference material preparation
    • European Pharmacopeia requirements for reference standards

    Typical usage ratio

    • Generally 0.01–0.1 g per synthesis batch, modulated by intended analyte concentration and detection method sensitivity; micro-quantities required for routine calibration or limited-lot reference standard production.

    Downstream process integration

    • Added during targeted organic synthesis or derivatization reactions, typically at the starting point of molecular probe or standard compound preparation, followed by purification and identity confirmation by HPLC or NMR analysis.

    Final product types

    • Certified calibration and reference standards for pharmaceutical and food analysis
    • Custom analytical research compounds for forensic, toxicological, and clinical laboratories
    • Ligand libraries for in vitro assay development
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride—A Deep Dive into Our Process and Its Benefits

    From Core Synthesis to Reliable Delivery—The Journey Behind Every Batch

    The path from raw materials to a refined compound like 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride isn’t straightforward. From a manufacturer’s viewpoint, consistent quality doesn’t just happen. Years of hands-on process improvement taught us that skipping real control at any step spells future headaches—our investment starts with precision in incoming material assessments and doesn’t let up until packed product leaves the warehouse.

    We commit to producing 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride that meets the performance standards needed by research teams and formulators. Taking shortcuts degrades the utility of the product in downstream synthesis, throws off anticipated reaction yields, and can undermine trust for years. We know this compound is more than a line in a catalog; it is a piece of research infrastructure. Every lot coming from our reactors has a story rooted in repeatable chemistry and direct experience with what can go wrong if overlooked.

    Purity and Specifications—Built By Experience, Not By Guesswork

    Even slight variations in purity or moisture can derail sensitive research and product development. Frequent sampling and analysis by our in-house team let us catch outliers early. Laboratories conducting structure-activity relationship studies or those looking for reliable intermediates quickly notice the difference. We've found that maintaining a minimum purity above 98% ensures stability and application value. Lower thresholds tend to bring unforeseen reactivity and yield drops, lessons learned the hard way in earlier years when lesser market requirements drove industry complacency.

    Our process includes drying steps that keep moisture content in check, reducing degradation risks during storage. Off-gassing problems stopped after we modernized storage and packaging, a decision that reflected both customer feedback and our operators’ suggestions from day-to-day handling.

    Model and Chemical Backbone—What Sets It Apart

    This compound offers both a rigid tetralin ring system and an imidazoline segment, making it useful as an intermediate in pharmaceutical and specialty synthesis. Experience shows that the compound’s dual nature—aromatic and heterocyclic—gives it versatility across several protocols, whether building more complex heterocycles or acting as a precursor in ligand design. Not every analog offers this combination; either the ring system introduces steric bulk too soon, or the imidazole core proves unstable during scale-up. We see researchers struggle with substitutions that promise cost savings but result in failed reactions or challenging purifications. Our process keeps the balance between performance and manageability, so end users don’t need to worry about solvating issues or unexpected isomer formation that crops up with lower grade material.

    Building Trust—Traceability, Transparency, and Real-World Testing

    Questions about how a batch was made, what grades of solvent were used, or the route taken to synthesize aren’t academic exercises for us. We track each batch—from sourcing of alkylating agents to in-process controls and all final wash stages. If an end user requests batch records for regulatory or troubleshooting purposes, we can show exact data, timelines, and even operator names for every cycle. That level of transparency comes from our years navigating audits from pharmaceutical clients and meeting preclinical supply standards.

    We don’t base our protocols on hypothetical scenarios. We send samples to long-time R&D partnerships, solicit feedback, and build product improvements around real-world use—not just from a set of numbers generated in a glass-walled lab, but from feedback that comes from post-reaction analysis, solubility assessments, and even tips from chemists who use this class of compounds in day-to-day projects.

    The Difference From Related Imidazole Derivatives—Lessons From the Bench

    Experience taught us that, among structurally related imidazole hydrochlorides, the tetralin-1-yl substitution delivers the best combination of solubility and reactivity. Chemists running parallel screens often compare analogs in cross-coupling or ring closure reactions, and our records show repeated orders come from teams facing inconsistency from generic products. We’ve tested competitive samples that claim similar performance; small differences in synthetic strategy (catalyst loads, workup efficiency, rinse protocols) turn into measurable batch inconsistencies.

    Offering a hydrochloride salt, instead of a free base, comes from practical feedback. Free bases tend toward air sensitivity and oiliness, often frustrating users during sample weighing and transfer stages. Our hydrochloride form stands up better to bench handling and gives a reliable powdery solid, which dissolves consistently in popular solvents as measured in our in-house verification runs. This seemingly minor difference earned us positive reports from laboratories who struggled with stickiness and poor reproducibility with free base options.

    Beyond the Brochures—Direct Impact in Real Chemistry

    We have seen our 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride unlock synthetic pathways that once hit repeated dead-ends. A research group focused on new ligand frameworks once approached us with solubility challenges; our controlled crystallization process produced material they could finally work with at scale, allowing progress in a project that had previously stagnated. These aren’t isolated anecdotes—they underscore how pure, consistent intermediate supply smooths the way for chemical innovation, rather than becoming the hurdle itself.

    The compound bridges key steps in medicinal chemistry campaigns. Its tetralin ring system imparts rigidity important for target binding in enzyme inhibitor programs, while the imidazoline fragment allows further diversification by alkylation or condensation routes. Slow reaction rates, impurity build-up, or stray isomer formation are frequent pain points with alternate sources—our protocols close those gaps, stemming from our own troubleshooting and collaborative development with both academic and industrial teams.

    Handling, Storage, and Shelf Life—Practical Insights from Daily Operations

    Our operators understand that no shelf stability comes by accident. We store material under nitrogen, with relative humidity and temperature carefully controlled by automated systems, responding to variations flagged during routine quality reviews. Older storage practices—relying only on desiccant packs and standard jars—gave unpredictable shelf behavior and prompted unnecessary rework. We overhauled practices to reduce oxygen and light exposure, especially post-purification, since the compound’s aromatic core is prone to slow oxidative change. That move cut loss rates and reduced batch downgrades, which builds value for both our team and our customers.

    Laboratories often ask about best storage practices. Experiments with different packaging taught us that amber glass containers, with an extra inner seal and nitrogen flush, yield the best stability. Our samples monitored over twelve, eighteen, and twenty-four month intervals confirm that the product retains its analytical identity and performance under these conditions—critical information for clients purchasing larger lots for extended projects.

    Supporting Synthesis: Where This Compound Fits, And Where It Doesn’t

    The real measure of a chemical intermediate lies in its contribution to making something new—or in making a process more robust. The rise in complexity across drug discovery and materials science asks for more from intermediates like this one. Whether supporting stepwise Ligand Synthesis, acting as a precursor to tetrahydroquinolines, or feeding into chiral pool strategies, our experience shows this compound delivers consistent results. We have also observed that some processes, such as those seeking extreme steric hindrance or fully saturated ring systems, benefit from alternate intermediates. We share these insights freely, knowing our practical advice smooths out problems before they occur.

    We believe transparency about where our compound fits—where it excels and where chemistry demands something else—earns confidence and saves time for everyone. Researchers reach out to us after hitting snags with other options; our depth of experience helps quickly pinpoint whether this compound is the right match or whether a different substitution pattern or N-heterocycle structure will better handle their requirements.

    Safety Realities—Engineered for Reliable Use, Not Just for Compliance

    Having made, handled, and shipped this compound for years, our staff knows the importance of safe practices. All team members receive hands-on hazard training specific to imidazole chemistry and hydrochloride salt management, extending well beyond general industry guidelines. Our hazard control protocols were shaped not by abstract standards, but by real plant incidents—solvent vapor monitoring, routine purge testing, and redundancy in emergency air handling make a difference in the real world. Safety sheets outline basics, but we have learned to expect the unexpected, especially when scaling up or running large-batch operations.

    Stable packaging, secure transit, and focused storage discipline aren’t add-ons; they form the backbone of reliable product delivery. Once, we encountered a transportation mishap that taught us quickly about the need for custom-designed drums for hygroscopic materials like this. Since then, specialty liners and reinforced closures come standard. Every improvement has a story rooted in our direct experience, and each new challenge adds to our knowledge base, making the product safer and easier to use for everyone.

    Working Side by Side With Chemists—How Feedback Builds Better Product

    Direct conversation with users—whether in academic labs or industrial pilot plants—guides product refinement far more than any catalog description ever could. One formulary team reported trouble dissolving sample product for a particularly challenging sequence. Their feedback prompted us to modify particle size distribution slightly, leading to better dispersibility and predictable solution preparation, and the change stuck after batch performance reviews showed gains across multiple applications.

    One of the greatest lessons we have learned comes from cases where chemists share data from both successful and failed runs. Sometimes a subtle byproduct profile reveals a needed adjustment in drying technique or purification. Those discoveries get incorporated into upcoming runs quickly, which benefits every user down the line.

    Choosing Our Product—The Results Reflect the Process

    Chemists who work with 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride from our line usually want more than a basic commodity. They look for assurances grounded in reality, traceable lots, honest feedback about what to expect in the flask, and the ability to dig into specifics if they need to troubleshoot their synthesis. Our open-door policy for technical discussions means clients benefit from shared expertise, not just a supply chain.

    The end result is more than a bottle on a shelf—it’s a tested, reliable intermediate that bridges the realities of process and performance. Whether the project involves discovery chemistry, pilot plant scale-up, or regular multi-kilogram manufacturing, we have seen this compound deliver the results researchers seek.

    Key Takeaways—What Years of Manufacturing Have Taught Us

    Every batch of 2-Tetralin-1-Yl-4,5-Dihydro-1H-Imidazole Hydrochloride has years of practical experience behind it: stubborn repeatability in production, constant improvement based on feedback, strategic investments in storage stability, and a shared sense of responsibility for what the product unlocks in our customers' work. Few chemicals play as broad a bridging role between early exploratory work and dependable process chemistry. Consistency, trust, and performance matter, and that drives every decision in our production protocols—ensuring no one who relies on this compound gets let down by surprises.