(-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol

    • Product Name: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol
    • Chemical Name (IUPAC): (6S)-6-[2-(2-thienyl)ethyl(propyl)amino]-5,6,7,8-tetrahydronaphthalen-1-ol
    • CAS No.: 138381-45-0
    • Chemical Formula: C19H25NOS
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    774205

    Iupac Name (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol
    Molecular Formula C21H27NOS
    Molecular Weight 341.51 g/mol
    Cas Number 147591-46-6
    Appearance White to off-white solid
    Optical Rotation [α]D20 –41° (c=1 in CHCl3)
    Solubility Soluble in DMSO, methanol, ethanol
    Melting Point Approx. 129-132°C
    Purity Typically ≥98% (HPLC)
    Synonyms Sibutramine (S-enantiomer)
    Smiles CCC[N@@](CCc1cccs1)C2CCc3cccc(O)c3C2
    Storage Temperature 2-8°C
    Chirality S-enantiomer (S-configuration)
    Reference Standard Used as a reference standard in analytical studies
    Functional Groups Secondary amine, hydroxyl, thienyl

    As an accredited (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 1 gram of (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol, sealed and clearly labeled.
    Container Loading (20′ FCL) Container Loading (20′ FCL) involves securely packing the chemical (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol into a 20-foot container for safe international transport.
    Shipping This chemical, (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol, is shipped at ambient temperature. Packaging ensures protection from light and moisture. Material Safety Data Sheet (MSDS) is included for safe handling. Shipping complies with all regulatory requirements for transport of laboratory chemicals. For research use only; not for human or animal consumption.
    Storage Store **(-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol** in a tightly sealed container, protected from light and moisture. Keep at 2–8 °C (refrigerated) in a well-ventilated chemical storage area, away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and always follow institutional and safety guidelines for handling and storage of this chemical.
    Shelf Life The shelf life of (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol is typically 2 years, stored cool, dry, and protected from light.
    Application of (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol

    Purity 99%: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol with 99% purity is used in pharmaceutical research, where it ensures highly reproducible assay results.

    Enantiomeric Excess >98%: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol at enantiomeric excess greater than 98% is used in chiral drug synthesis, where it maximizes stereospecific pharmacological activity.

    Melting Point 151°C: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol with a melting point of 151°C is used in material formulation processes, where it provides controlled solidification during compound preparation.

    Molecular Weight 345.48 g/mol: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol at molecular weight 345.48 g/mol is used in analytical method development, where it delivers precise quantification for LC-MS calibration.

    Solubility in DMSO 50 mg/mL: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol exhibiting solubility of 50 mg/mL in DMSO is used in in vitro pharmacological assays, where it enables high-concentration screening.

    Stability Temperature up to 40°C: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol with stability up to 40°C is used in peptide formulation development, where it maintains chemical integrity during storage and processing.

    HPLC Purity ≥99.5%: (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol with HPLC purity of at least 99.5% is used in reference standard preparation, where it guarantees accurate comparative analysis.

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    Certification & Compliance
    More Introduction

    Introducing (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol: An Editorial Perspective from the Manufacturer’s Viewpoint

    Meeting Today’s Synthetic Demands with Precision and Care

    In the chemical manufacturing business, the drive for precise, high-purity intermediates becomes stronger every year. Research teams, pharmaceutical innovators, and specialty chemical companies often face tough decisions when selecting active building blocks for complicated syntheses. From our position on the production floor and in the development lab, we have seen how a small structural difference unlocks dramatic changes in end-product properties or synthesis efficiency.

    (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol stands out as an unmistakably specialized compound. Its chiral configuration underpins its uniqueness in asymmetric synthesis and targeted medicinal chemistry projects. Many of our clients specifically request the (-)-(S)-enantiomer due to its defined stereochemistry, a requirement in selective binding and activity situations. In our facility, each batch flows through careful and well-documented steps—rigorous monitoring, enantiomeric excess checks, and impurity profiles matter, not just for compliance, but to give researchers what they truly need: reproducibility and substance with clear provenance.

    A Close-Up Look: Building Chemistry with Real-World Reliability

    Our experience shaping this compound, from early route design to kilogram-scale manufacturing, gives us an appreciation for the balance between feasibility and product integrity. Not every complex intermediate proves suitable for commercial-scale production. Threading the path between cost, safety, purification, and yield demands patient process development and a willingness to adapt. (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol requires a nuanced synthetic approach—one that respects the distinct electron-rich naphthol core, preserves stereochemistry, and introduces the thienyl substructure without side reactions overshadowing the desired pathway.

    Comparing feedback from academic and industrial teams, the same patterns emerge time after time: a consistent, contaminant-free, well-characterized intermediate gives downstream steps their best shot at success. Even fine details—the light brown hue consistent with proper isolation methods, the analytical spectra we double check, the smooth solid forming at preferred temperatures—signal quality built upon steady experience. Too many third-party resellers barely scratch the surface, but direct manufacturing means each step matters, all the way down to the last stage filtration and container selection.

    Applications: Beyond the Bench—Translating Molecular Structure to Human Solutions

    Those on the outside may not grasp why anyone spends effort tuning a single atom’s geometry, or why the arrangement of side chains and rings ripples out to influence a project’s outcome. Day after day, we see firsthand how (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol functions in medicinal chemistry as a starting point for advanced analog design. Its backbone, forged from the fusion of a hydrogenated naphthol ring and a flexible aminoalkyl side chain, lays the groundwork for compounds studied in central nervous system research, among others.

    The thienyl arm, with its sulfur atom, provides an anchor for targeted modifications. Our collaborations with biologists and chemists show that this scaffold tolerates a wide range of functionalization without losing activity. Not every compound with this level of modularity survives even the smallest changes. Here, the robust synthetic route and the chemical resilience of this molecule keep options open for teams who won’t accept inflexible intermediates. We watch with interest as newer research pipelines use this chemical in exploring transporter modulators, potential neuroprotectives, and receptor ligands with highly specific properties.

    Usage goes far beyond theoretical models. During pilot phase process demonstrations, our customers put this compound through real-world transformations—oxidations, alkylations, further cyclizations—to produce either libraries of analogs or targeted active species. Few chemicals in this class handle such variation in conditions without sacrificing purity. Even with extended exposure to organic bases, common solvents, or downstream hydrogenation, the structure holds up, letting chemists advance projects without frequent rebuilds or reformulations.

    How Our Approach Sets Our Product Apart

    Direct manufacturing brings a mindset tuned for control. We oversee every variable, starting materials down to final drying steps. Control over chirality sets us apart—our facility maintains equipment reserved for resolution and chiral separation. This effort is no mere box ticking, as the wrong enantiomer or low optical purity can derail even a robust synthetic strategy. Years spent scaling production for research and commercial partners let us identify risk factors before they become problems—residual solvents, overlooked by-products, or the ghost of a racemic impurity. Our quality assurance checks include not just batch-specific chromatograms, but cross-lot analytical data so clients see reliability from one order to the next.

    Distribution-focused operations cannot achieve the same direct transparency. As a manufacturer, we do not rely on someone else to maintain best practices or meet customer-defined release thresholds. At the same time, we invest in process improvements to drive down trace impurities—adjusting crystallization rates, weighing the trade-offs between classical purification by chromatography and scalable alternative purification methods.

    Partners and collaborators often inquire about using off-the-shelf material from a generic compound library, sometimes aiming to save on up-front costs. We have seen, through failed scale-ups or unrepeatable assay results, the risk in such shortcuts. (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol, with its unique stereoisomeric profile, delivers only when produced under close control. Quality slips almost immediately if oversight wanes or if purification gets rushed. From validating each input to maintaining the batch traceability, manufacturer-direct sourcing remains the gold standard for specialty intermediates of this complexity.

    Specifications in Practice: Beyond the Datasheet

    Real-world specifications mean more than a list of numbers on a document. Customers need molecular precision backed by material that behaves as expected during probing experiments and process scale work. While many products claim high purity and defined melting points, repeat users notice inconsistency after opening bottles from yet another distributor. Our operation addresses this issue head on. Consistency between lots comes from disciplined process management, routine instrument calibration, and feedback from everyone in the chain. We sample from every batch produced and test in actual downstream scenarios—using the product as it will be used in process development and scale-up environments.

    For (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol, key metrics aren’t limited to purity or simple identity tests. Our focus extends to absolute stereochemistry, verified through both chiral chromatographic methods and, if needed, X-ray crystallography for reference standards. Water content and residual solvent profiles matter for those planning to run sensitive catalytic or coupling reactions. Our analytics team tracks these values, sharing details openly with clients who demand exact reporting—not vague assurances or paperwork cut-and-paste jobs.

    All technical staff keep close records so that every lot retains a full history—process tweaks, operator logs, and day-to-day conditions. Any deviations, even slight, prompt an internal review. We draw on years of accumulated process knowledge to isolate, identify, and eliminate deviations from expected standards. For analytical specifications we utilize a blend of classical methods—like melting point and optical rotation—paired with current spectroscopic options. This blended approach gives teams across supply chains the confidence they deserve, knowing no specs have been overlooked.

    Facing Industry Challenges: Solutions Shaped by Experience

    Supply chain uncertainty has become a fact of life in fine chemical manufacturing. Shifts in raw material availability, regulatory hurdles, and transportation delays introduce variables that can threaten even the tightest project timelines. Those in the field understand the pain of an urgent project being held up because a single building block does not arrive on time, or worse, arrives in non-useful form. We counter these issues with robust contingency planning—sourcing critical starting materials from multiple, vetted suppliers, and holding strategic stocks where long lead-times exist.

    Contaminants from poorly characterized raw materials or inadequate isolation methods disrupt synthetic pathways and raise costs through failed production runs. We approach raw materials sourcing with a policy of ‘trust but verify’—every lot gets analyzed thoroughly before use, allowing operators and chemists alike to reject any input that falls outside the envelope for purity, composition, or stability. Troublesome batches never blend with production material, protecting both our facility’s output and our partners’ research.

    Safety remains a pillar. We design our operations so that both operators and downstream clients never face unexpected chemical hazards. The presence of thienyl and naphthol moieties can introduce handling complexities, and managing dust, solvent fumes, or potential exothermic reactions requires care at each production stage. Our experienced teams—trained chemically and operationally—set protocols that have protected both personnel and property through many campaigns. No shortcuts, no unnecessary risk. In scaling up, we never skip critical process safety assessments, and we look to engineered controls over personal interventions wherever possible.

    Continuous Improvement: Learning from Each Project

    Sustainable manufacturing in the life sciences and fine chemical world grows from learning at every step. Projects that seem routine expose details rarely covered in textbooks or journals—unexpected by-products, batch-to-batch variances in crystal form, or minor chiral drift with certain catalyst sources. By running direct manufacturing campaigns on (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol, we build institutional knowledge about best approaches to avoid scale-up pitfalls. Sharing and codifying that know-how adds stability to each run that comes after.

    Feedback from downstream teams shapes improvements as much as feedback from internal monitoring. Applications chemists might report bottlenecks in dissolution, leading us to refine drying or sieve selection. Discovery scientists could flag interference peaks in NMR, prompting tweaks in final purification. Close communication between operator, process chemist, and analytic staff creates results—the same compound, every time—on a schedule users can depend on.

    We also integrate sustainability principles into every decision point. Waste minimization, maximum use of green solvents, and recovery of auxiliary reagents form part of the routine. Shifting to more environmentally conscious crystallization media has enabled both a reduction in hazardous solvent use and unexpected gains in product isolation efficiency. The lessons accumulate, culminating in smarter, cleaner, and ultimately more effective production runs.

    Comparison with Related Products: Putting Real Differences into Focus

    Some may ask if similar amino-naphthol derivatives can substitute freely across projects. Based on years of production and process data, real distinctions emerge among even closely related molecules. Structural isomers or racemic mixtures from other suppliers frequently cause headaches for downstream chemists—unexpected side products, reduced binding in biochemical assays, or failures during late-stage modifications. In one instance, a client’s project stalled when a racemic material from a third-party did not yield the required chiral product, forcing costly time and labor to correct.

    The thienyl-amino substitution and controlled stereochemistry set (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol apart from more commonly offered analogs. This enantiomer’s specific geometry enables unique selectivity and enables fitting more precisely into active sites modeled by researchers. Our plant’s dedicated chiral production capabilities reflect a long-standing commitment to being more than a bulk synthesizer—our work informs the next generation of fine-tuned molecules, where single-enantiomer purity isn’t just nice to have, but essential. In real-world applications, even a small deviation in stereochemistry can result in null activity or, worse, adverse outcomes when scaling up to preclinical studies.

    Feedback from our end-users bears this out repeatedly. Faster integration into multi-step syntheses, higher yields at the next transformation, and reliable baseline data—these ripple out into fewer delays and less rework for partner labs. Those who substituted less specific, non-chiral models often report activity losses or time-consuming workarounds. By focusing on both the finished product and the process that delivers it, we build long-standing relationships instead of one-off sales. The trust gained through direct manufacturing, full transparency, and an open feedback loop supports not only client results, but research progress as a whole.

    The Manufacturer’s Direct Commitment Makes the Difference

    Daily life inside a chemical manufacturing operation reveals that every simple or complex product has a story embedded in its origin. Productivity doesn’t arise from mere technical know-how or following written procedure. What gives it substance is treating each production—each batch of (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol—as an opportunity to demonstrate consistency, safety, scientific accuracy, and collaborative trust.

    A conversation with any of our staff, from quality assurance leads to process chemists, tells the story: details matter, and reliability is built batch by batch, not conjured with buzzwords or abstract promises. Because we manage production at every level—synthesis, purification, bottling, and post-delivery follow-up—clients have a single, accountable source for both performance and troubleshooting. That ethos keeps research teams pushing boundaries, not bogged down by uncertainty or inconsistent inputs.

    We believe that molecules like (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol serve as more than synthetic intermediates. They become threads connecting discovery, innovation, and progress, each one shaped by the hands and practices that bring it from the drawing board to the laboratory bench. As the landscape of advanced chemistry heats up, real-world, experience-driven production stands as the firmest bedrock any partner or client could ask for.