4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1)

    • Product Name: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1)
    • Chemical Name (IUPAC): 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride
    • CAS No.: 147635-77-6
    • Chemical Formula: C7H9NS·HCl
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    450952

    Product Name 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1)
    Cas Number 132335-44-3
    Molecular Formula C7H11NS·HCl
    Molecular Weight 193.70 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water
    Melting Point 194-198°C
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms Tetrahydrothieno[3,2-c]pyridine hydrochloride
    Smiles C1CCN2C=C(S1)CC2.Cl
    Inchikey UQCHKCIHZYKGKX-UHFFFAOYSA-N
    Ph Of Solution 3.0 - 5.0 (in water)
    Hazard Class Irritant

    As an accredited 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, tamper-evident HDPE bottle containing 25 grams of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1), labeled with hazard and storage information.
    Container Loading (20′ FCL) 20′ FCL holds about 11-13 MT of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1), packaged in drums or bags.
    Shipping 4,5,6,7-Tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) is shipped in tightly sealed containers under dry, cool conditions to prevent degradation. Packages are clearly labeled with hazard information and handled according to local, national, and international regulations for safe transport of chemical substances. Suitable for laboratory use only.
    Storage Store 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) in a tightly sealed container, protected from moisture and light, at room temperature (15–25 °C) in a dry, well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and limit exposure to air and humidity to prevent degradation or hydrolysis.
    Shelf Life 4,5,6,7-Tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) typically has a shelf life of 2 years when stored tightly sealed, protected from moisture.
    Application of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1)

    Purity 98%: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) with 98% purity is used in pharmaceutical intermediate synthesis, where high compound integrity ensures enhanced reaction yield.

    Molecular Weight 181.7 g/mol: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) of 181.7 g/mol molecular weight is used in medicinal chemistry research, where precise molecular weight enables accurate dosing calculations.

    Melting Point 164–168°C: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) with melting point 164–168°C is used in formulation studies, where thermal stability supports consistent compound performance.

    Particle Size < 10 µm: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) with particle size below 10 µm is used in tablet production, where uniform particle size enhances dissolution rates.

    Stability Temperature up to 60°C: 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) stable up to 60°C is used in storage applications, where thermal resistance maintains compound efficacy during processing.

    Free Quote

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    Certification & Compliance
    More Introduction

    4,5,6,7-Tetrahydrothieno[3,2-c]pyridine Hydrochloride (1:1): Practical Experience and Insights from Our Production Floor

    Direct Sourcing from the Plant—What It Means for Quality and Consistency

    Producing 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (1:1) straight from the manufacturing line, every step carries our hands-on fingerprint. Customers often ask about the difference between pulling product directly from a manufacturer's synthesis and picking up the same item from downstream vendors. On a busy day, as vessels are loaded and raw materials checked, traceability and reliability don’t feel like empty words. Our teams stand by the reactors with logs marked by real individuals and every batch comes with process records that highlight not just compliance, but nuances we notice batch-to-batch.

    This compound's hydrochloride form brings together stability in storage and handling, which technicians on our floor appreciate during packing. As the crystals settle, humidity, airflow, and even transfer speed leave their imprint on the finished material. Through years of watching these cycles, we’ve learned which environmental tolerances prevent clumping or uneven particle development—details too easy to gloss over for those further removed from synthesis.

    About the Model and Specifications—Bench to Bulk, No Theoretical Gaps

    Stepping onto our production floor, one finds the specification blackboards updated not by distant committees but by working chemists who measure each batch’s color, flow, and purity by hand before signing off. Our standard manufacturing offering focuses on pharmaceutical and fine chemical needs where consistent input saves valuable hours downstream. The typical lot appears as a white to off-white crystalline powder, but the difference comes in the process fit. For clients scaling a pilot project, our kilo-scale output matches exactly to larger bulk, with no need for revalidation of upstream parameters.

    We regularly verify melting range, moisture content, and residual solvent profiles well past tactic compliance. If a value drifts within normal statistical bands but looks odd based on our experience, the batch never proceeds. Staff know which points in the synthesis can leave odd signatures in the final readout—details overlooked by simple COA checks. Through daily experience, most plenty can be cross-referenced with long-term stability records, so anomalies are found early, not years down the line. Specifications stay grounded in real measurements, as our team understands how slight impurity shifts can impact downstream transformations or formulation processes.

    Hands-on Handling Insights

    Years of direct practice with 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride mean we know its quirks during storage and dispensing routines. The powder handles cleanly—no excessive electrostatic charge or stubborn clumping under normal humidity, which can often be an issue with halide salts. After long cycles of trial and error, we realized controlling the final drying parameters produces a directly usable product. Staff are fully briefed on light protection and moisture containment because even a minor lapse in packaging protocol can register as a loss of performance years later.

    Ordering from a source without direct production oversight often brings surprises—variable bulk density, unexpected agglomerates, or traces from prior processes. Our customers rarely encounter these headaches because we recognize the value in transparent, open tracking from start to finish. Any batch—whether sampled two months after production or kept for archival record—shows the result of careful process oversight.

    Core Applications: Seen from the Manufacturer’s Perspective

    Demand for this compound mainly comes from custom synthesis, pharmaceutical intermediates, and fine chemical sectors. Our location close to both pharma and API development groups gives us regular feedback about the suitability of our lots for various coupling, alkylation, and cyclization steps. Academic groups sometimes visit to compare our batch records against published synthetic routes, and they often notice subtle differences in yield or side product profiles, rooted in the upstream consistency we maintain.

    We’ve also witnessed applications expand as the reliability of supply improved. Formulators rely on our compound for experimental drug synthesis when commercial API routes require thienopyridine backbones. Unlike off-the-shelf distributors, we get granular requests from research chemists eager to see impurity fingerprints, stereochemical confirmation, and reproducibility checks. Across dozens of projects, we see how controlling isomer content and avoiding cross-contamination with similar heterocycles can save months of troubleshooting later in the pipeline.

    Role in Scale-Up and Reproducibility

    No one feels the pain of scale-up headaches more than a process chemist trying to move from bench to pilot. Our batch logs record not just the target yield and purity, but also reaction time, reagent charge order, solvent grade, and environmental variables that may sway a key reaction. That background allows us to support scale transitions where the nuances of this compound’s preparation (such as the effect of minor temperature drifts or rapid addition of reagents) change output properties.

    Feedback over the years has shown us that process fingerprints often show up only at scale. Reproducibility starts with the way solvents are dried, reactors are cleaned, and intermediates are isolated. Customers working with diverse formulation methods regularly report smoother transitions using our material—less downtime to troubleshoot off-spec input, fewer reprocessing cycles, and no unexpected incompatibilities with downstream excipients. Many times, we track a lot from initial production, through pilot validation, to final regulatory filing, giving us an end-to-end look at where deviations typically occur and how we can correct them on future runs.

    Comparison Against Other Sources and Compound Variants

    Not all sources for 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride show the same stability, impurity control, or shelf-life. Laboratories testing with multiple vendors often report batch-to-batch differences, manifesting as off-flavors, color drift, or solubility issues. Our synthesis sequence avoids common pitfalls involving catalyst residues or polymorphic mix, which can create inconsistencies in formulation or scale-up.

    Some suppliers offer material in free base form or as alternative salts. From experience, the hydrochloride version provides a safer and more predictable profile, both in chemical transformations and in handling. Free base alternatives tend to absorb atmospheric moisture and degrade more rapidly, causing reliability headaches for clients who need to store or transport material across distances. Our hydrochloride remains stable through standard shipping, requiring no special inert atmosphere packaging.

    We also see distinctions in how customers apply this compound, depending on source reliability. End-users in synthetic labs, seeking efficient product isolation or clean subsequent transformations, prefer our offerings due to low residual solvent levels and highly consistent particle size. Repeated process cycles in-house show a remarkable drop in failed reactions due to off-stoichiometry or contaminated inputs when switching from typical distributor sources to direct-from-plant material.

    Quality Assurance Rooted in Real-World Experience

    Plant-level experience drives our quality program. Inspectors do not work from abstract checklists; they bring years of hands-on exposure to subtle changes in reaction color or odor that signal off-normal operation. Batch signoff occurs only after physical inspection and comparison with historical controls, not just passing an IR readout or HPLC trace. We see the finish line for each order—the actual product handed to a working chemist, not a theoretical data-sheet.

    Any deviation, from crystal habit to packaging tightness, signals a process break. In our operation, these are caught early thanks to direct feedback from packing teams and end-users who return not just with grievances, but with detailed performance notes. There is no stage at which quality becomes a box-ticking formality; every shift retains a memory of previous runs, adjusting as seasonal, supply, or regulatory factors require practical change.

    Sustainability and Safety as Embedded Habits

    Modern chemical production demands responsibility beyond minimum standards. Our facility organizes waste recovery and solvent recycling with engineers who work close to the reactors—every gallon saved has visible impact. Offerings reflect transparent reporting on secondary emissions and occupational hygiene, since the same staff cycle through synthesis, drying, and packing operations. Checks for exposure, cross-contamination, and best practices follow internal logic—protecting both product and personnel.

    Safety protocols have grown side-by-side with our internal training. The routine never slips—from barcode tracking of in-process samples to respirator use during loading. If we spot an unusual reaction byproduct or venting, those observations circulate across teams in real time, leading to immediate adjustments. This culture of vigilance keeps both product quality and worker safety high, and prevents downstream issues that vendors further from source rarely catch.

    Traceability as a Living System

    Each lot of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride draws from a history tracked across internal systems, storage logs, and repeat customer feedback. Visitors to our plant can walk through the sequence from incoming raw materials (backed by supplier trace), to batch blending, to drying, and on to finished goods. Order records connect not just to COAs but to operational notes—if an operator writes, “slower crystallization, extended dry,” those records follow the batch.

    Clients requiring regulatory scrutiny, particularly in pharmaceutical or critical chemical contexts, rely on our full-trace output. By producing in-house, we provide complete access to provenance and in-process controls. That level of transparency improves audit outcomes and speeds regulatory responses—a benefit nearly impossible to replicate for brokers or distant distributors.

    Responding to Customer Needs—Learning from Practical Challenges

    Direct production experience sharpens our ability to adapt. Customers with atypical synthesis constraints, exotic solvents, or unusual purity needs call out specifics that help refine our routines. On several occasions, a pilot-phase trial exposed the effect of an overlooked micro-impurity that interrupted downstream coupling, leading us to investigate and tighten an extraction parameter or adjust a heating profile.

    The process of production means bumps and corrections are inevitable. Open channels for feedback, whether from academic clients or process-scale partners, guide us more effectively than distant market surveys. If a formulation chemist flags delayed solubility or slight odor drift, we cross-check across finished goods inventory and, more often than not, the remedy emerges from shared experience between our technical staff and bench chemists. This interactive loop tightens control and produces material attuned to real-world needs, rather than theoretical ideals.

    Critical Takeaways: Why Chemical Origin Matters

    Most end-users don’t notice raw material origin until an issue arises. As manufacturers, the knock-on effects from minor upstream deviations magnify as complexity increases downstream—especially in regulated, high-purity applications. Unlike brokers, we own each stage and can respond instantly if a client sees anomalies. Not a quarter passes without a customer returning with gratitude for the uninterrupted run delivered by our best batches, often after a previous batch from elsewhere derailed a project.

    Feedback over years underscores one truth: direct-from-source material provides peace of mind. Consistency in color, density, and performance spares our partners from unnecessary troubleshooting and allows smoother audits. Our process delivers that confidence, and the record shows fewer headaches and unplanned reformulations for our clients.

    Adapting to Today’s Industry Pressures

    With regulations tightening and downstream auditing on the rise, buyers shift toward single-source, traceable lots. The ability to provide detailed process documentation, impurity mapping, and responsive upscaling grows more valuable each year. Staff see market shifts firsthand—a sudden policy update or customer project expansion becomes not just a new challenge, but an occasion to revisit and enhance our process.

    Rather than waiting for external audits to flag issues, we invest in plant-scale monitoring—cross-referencing each batch with global customer reports and trending performance over months or years. This proactive stance means our product maintains relevance as strict compliance and process transparency rise in importance.

    Moving Forward on a Firm Foundation

    Daily experience on the manufacturing floor affirms our belief that close stewardship, open channels for field feedback, and relentless focus on technical detail bring lasting value to clients investing in 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride. Whether facing a regulatory audit, tackling laboratory bottlenecks, or aiming for long-term lot stability, our in-house expertise shapes every granule shipped.

    Through many years of direct engagement, constant process refinement, and trusted relationships with users ranging from medicinal chemists to process engineers, we continue to tailor each batch to the evolving requirements of high-stakes chemical synthesis. This commitment distinguishes the direct manufacturer’s role from that of temporary intermediaries, ensuring ongoing improvement and dependability.

    Conclusion—A Product Defined by Practical Commitment

    The real strength behind each lot of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride lies not in specification sheets but in how production teams, quality specialists, and client partners collaborate. The value comes from lived experience, day-to-day control, and willingness to adapt based on feedback. The result is a compound that speaks for itself in both consistency and performance—attributes only possible with direct manufacturing stewardship.