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(R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride

    • Product Name (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride
    • Alias (R)-BAT-HCl
    • Einecs 872365-37-6
    • 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

    528785

    Product Name (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride
    Cas Number 179798-18-4
    Molecular Formula C11H14ClNO2S
    Molecular Weight 259.75
    Physical State Solid
    Appearance White to off-white powder
    Solubility Soluble in water
    Optical Rotation [α]20/D +20° (c=1, H2O)
    Purity Typically >98% (HPLC)
    Storage Temperature 2-8°C
    Synonyms D-CBT HCl; D-CBT hydrochloride
    Chemical Class Amino acid derivative
    Inchikey SXMEKYJMDSQMGP-BPXNURHXSA-N
    Smiles C1=CC2=C(C=C1)SC=C2C[C@H](N)CC(=O)O.Cl

    As an accredited (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride 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 1 gram of (R)-3-Amino-4-(3-benzothienyl)butanoic acid hydrochloride, labeled with safety and purity details.
    Shipping (R)-3-Amino-4-(3-Benzothienyl)butanoic Acid Hydrochloride is shipped in tightly sealed containers under ambient or cool conditions to ensure stability. The package is labeled according to regulatory guidelines and handled as a non-hazardous chemical unless otherwise specified. All documentation and safety data sheets are included for safe transport and handling.
    Storage (R)-3-Amino-4-(3-Benzothienyl)butanoic acid hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep it at a temperature of 2-8°C (refrigerated), away from incompatible substances such as strong oxidizers. Ensure proper ventilation in the storage area and clearly label the container. Handle with appropriate personal protective equipment to prevent exposure.
    Application of (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride

    Applications of (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride in Industrial Manufacturing

    (R)-3-Amino-4-(3-Benzothienyl)butanoic acid hydrochloride, as a chiral, high-purity amino acid derivative, enables downstream manufacturers to drive complex synthesis within pharmaceutical and specialty chemical sectors. Our on-site production capabilities and controlled batches ensure consistent integration into high-value applications where molecular precision and traceability are mandatory.

    1. Chiral Building Block for Anticonvulsant API Synthesis

    The compound functions as a critical intermediate during the synthesis of antiepileptic active pharmaceutical ingredients under strict cGMP environments. Its chirality and chemical stability are pivotal in scalable production of next-generation central nervous system therapeutics, allowing consistent batch repeatability and regulatory traceability directly from raw material addition through to final purification.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP (Part II) for pharmaceutical starting materials
    • USP General Chapter <823> for raw material controls
    • FDA 21 CFR Part 211: Finished Pharmaceutical Good Manufacturing Practices

    Typical usage ratio

    • Application in reaction feeds: 0.5–1.2 molar equivalents relative to synthon, adjusted by process yield and final API purity requirements.

    Downstream process integration

    • Material enters as a primary amine source during chiral amide or amide bond coupling, typically following activation of carboxylic function. Downstream purification steps maintain enantiopurity, with in-process analytical controls at each stage.

    Final product types

    • Active pharmaceutical ingredients (APIs) for anticonvulsant tablets
    • Pharmaceutical-grade pre-formulated bulk intermediates

    2. Intermediate in Development of Novel GPCR Modulators

    Downstream drug discovery laboratories utilize this compound as a modular unit for the construction of benzothiophene-based analogs targeting G protein-coupled receptors. High specificity in its molecular structure allows for controlled functionalization operations in medicinal chemistry pipelines, supporting rapid lead optimization during preclinical development.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 for research chemical manufacturing
    • USP <1092> for laboratory reagents

    Typical usage ratio

    • Applied in solution-phase synthesis at 1.0 equivalent to the electrophile; adjusted as per reactivity and biological screening outcomes in iterative cycles.

    Downstream process integration

    • Material added during early-stage amide bond formations or selective aryl substitutions. Follows subsequent transformation and high-throughput screening, with batch documentation to meet compound library traceability protocols.

    Final product types

    • Lead candidate molecules for neuropsychiatric indications
    • Preclinical small-molecule tool compounds for pharmaceutical development

    3. Precursor for Chiral Auxiliary Synthesis in Asymmetric Catalysis

    Custom catalyst manufacturers use this amino acid derivative to generate chiral auxiliaries designed for stereoselective synthesis of fine chemicals. The benzothienyl moiety supports subsequent ring-closure and directional reactivity, enabling large-scale batch or continuous synthesis under validated ISO systems for specialty organocatalysts and ligands.

    Industry compliance standards

    • ISO 9001:2015 for batch production quality management
    • REACH Regulation (EC) No 1907/2006 for safe chemical handling and supply
    • Chemical Hazard Classification: GHS/CLP

    Typical usage ratio

    • Utilized between 5–10% w/w relative to main substrate, with adjustments depending on the desired chiral auxiliary loading and target enantiomeric excess.

    Downstream process integration

    • Serves as a critical reagent in the first step of auxiliary construction, typically through regioselective acylation followed by further functionalization in a protected environment.

    Final product types

    • Chiral auxiliaries and ligands for pharmaceutical synthesis
    • Specialty catalysts for fine chemical manufacturing

    4. Analytical Standard for Quality Control in Benzothienyl Compound Detection

    Accredited analytical laboratories integrate this substance as a reference standard for developing and validating chromatographic and spectrometric methods used to quantify benzothienyl group-containing products. Its high purity and well-characterized spectral profile make it suitable for regulatory analytical procedures within GMP-compliant quality control environments.

    Industry compliance standards

    • ISO/IEC 17025: General requirements for the competence of testing and calibration laboratories
    • USP <621> Chromatography method validation
    • FDA Analytical Procedures and Methods Validation

    Typical usage ratio

    • Used at standard concentrations of 10–100 μg/mL in analytical runs; final concentration set by instrument sensitivity and required method detection limits.

    Downstream process integration

    • Prepared as part of calibration standards for validation of HPLC/UPLC or LC-MS analytical protocols. Supports ongoing lot release and raw material identification testing within regulated production streams.

    Final product types

    • Pharmacopeial reference samples
    • Certified analytical calibrators

    5. Research Reagent for Neurobiological and Pharmacological Studies

    Academic and contract research facilities purchase this compound for controlled investigations into neuronal receptor interactions and structure–activity relationships. Its defined stereochemistry and functional groups permit targeted modifications and in vivo evaluations, supporting peer-reviewed research under recognized laboratory standards.

    Industry compliance standards

    • GLP compliance for nonclinical lab studies (OECD Guidelines)
    • Institutional Animal Care and Use Committee (IACUC) protocols for in vivo models
    • ISO 17034: Reference Material Producers

    Typical usage ratio

    • Applied in cell culture or in vivo models at 0.1–10 μM, titrated according to downstream bioassay endpoints and exposure assessments.

    Downstream process integration

    • Dissolved or derivatized prior to cell-based assays, patch-clamp recordings, or pharmacokinetic studies. Documentation ensures batch-to-batch consistency for publication and regulatory filing.

    Final product types

    • Data packages for neurochemical mechanism research
    • Published findings in pharmacology studies
    Free Quote

    Competitive (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride 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.

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    Certification & Compliance
    More Introduction

    Exploring (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride: A Closer Look from Our Manufacturing Floor

    The Chemistry Behind (R)-3-Amino-4-(3-Benzothienyl)Butanoic Acid Hydrochloride

    Long days in the plant have taught us that each compound we craft brings its own set of challenges and opportunities. (R)-3-Amino-4-(3-Benzothienyl)butanoic acid hydrochloride, a chiral amino acid derivative, stands out in the catalogue. Fingertips stained from thousands of syntheses tell us that achieving purity and correct stereochemistry is not just a checkbox for us—it’s the lifeblood of our responsibility toward researchers and pharmaceutical developers.

    Our batches offer stable hydrochloride salt forms and consistently hit the intended enantiomeric excess, not because specifications demand it, but because production teams live by the motto: “No shortcuts.” This material often finds its way into CNS drug discovery projects and structure-activity relationship explorations in both academic and pharmaceutical circles. We feel a certain pride knowing our work feeds into early-stage research that could impact patient lives years down the road.

    Model, Specifications, and Lot Consistency

    Over time, we have fine-tuned the process from the first grams made on lab benches to multi-kilogram lots flowing from commercial reactors. Model numbers and catalog designations may be straightforward on the site, but behind each product label lies the hard-earned wisdom of scale-up chemists and quality analysts.

    Typical specifications see purity values exceeding 98% and well-defined enantiomeric ratios. Achieving this consistently never comes down to just the LC and chiral HPLC prints: it means someone double-checks the crystalline form, watches for the tell-tale pinkish hue that warns of a side reaction, and reviews spectral data like a detective hunting for clues. From batch to batch, the goal isn’t just to match the paperwork—it is about delivering a substance that doesn’t let down a research team after weeks or months of investment in animal models, synthetic intermediates, or lead optimization runs.

    Direct Usage in Medicinal and Academic Chemistry

    The teams who buy this compound don’t see it as a mere commodity. They care deeply about consistency, physical handling properties, and time to delivery. The hydrochloride salt arrives stable, free-flowing, and straightforward to weigh and dissolve, lowering error risk for scientists deep into projects with tight schedules. Real-world experience tells us that a well-crystallized hydrochloride trumps most unprotected amino acids when it comes to handling and storage—a point that has saved more than one customer from tuning their protocols for material that clumps or degrades prematurely.

    We know firsthand some researchers use (R)-3-amino-4-(3-benzothienyl)butanoic acid hydrochloride as a GABA analog in the development of potential CNS-active molecules, given its structural similarity to known pharmacophores. Our chemists are careful to ensure the chiral purity matches the requirements for receptor binding studies, so off-target enantiomeric contaminants don’t muddy SAR conclusions. The feedback loop from bench to batch records and back again—sometimes spanning continents—shapes each production cycle.

    Comparisons to Other Amino Acid Analogs and Bulk Chemicals

    Colleagues sometimes ask how the product stacks up next to related analogs. Through years in the manufacturing bay, we have worked with many chiral intermediates and specialty amino acids: their quirks become familiar over time. Unlike products supplied in base form or as racemates, this hydrochloride salt offers both stability and resolvable crystal properties. Its optical rotation and melting point help catch even the smallest process deviations early.

    Standard beta-amino acids might cover certain needs, but the three-benzothienyl group imparts a unique electronic character. It alters receptor interactions significantly compared to simpler phenyl or alkyl substitutions. We have watched supply cycles for racemates shift as more teams prioritize cleaner, single-enantiomer intermediates. They have learned that bifurcated synthetic efforts only create new regulatory hurdles and repeat analyses, which can slow a development timeline by weeks. We focus hard on keeping our own process reproducible for exactly that reason.

    Why Consistency and Transparency Set Us Apart

    Stories float around our break room about the time a project team somewhere in Europe halted a lead candidate because the commercial batch they sourced deviated from their pilot sample. Unlike resellers who shuffle containers across borders, our name ends up on every certificate and invoice, and frankly, that honest connection matters. Every step is traceable to our in-house chemists: from sourcing the benzothiophene starting material, to resolving the chirality, to salting the final product with a carefully controlled acid process.

    Our analytical labs keep redundant records, not because the paperwork is fun (it is not), but because when a collaborator or customer calls, we want to lay out the whole lot’s processing timeline and specs with no guesswork. Over batches and years, we’ve trained ourselves and the next generation of process chemists that rigorous transparency solves problems before they grow roots. Due diligence on our end saves time for those who depend on our work.

    Addressing Challenges Unique to Chiral Amino Acids

    Manufacturing (R)-3-amino-4-(3-benzothienyl)butanoic acid hydrochloride is demanding, no doubt. Racemization risk persists through every temperature spike and pH swing. Some competitors cut corners with a quick quench or less precise pH control, but we learned the hard way early on that half-measures create headaches later.

    Surprisingly, side reactions sometimes spike from trace metal impurities in higher-volume prep. We combat this by swapping reactor liners and sticking to strict material transfer protocols. Years of process tweaks cut error rates and improved our ability to guarantee batch-to-batch continuity. Our plant’s investment in high-sensitivity NMR and chiral chromatography analysis wasn’t window dressing: it powerfully filters out small deviations invisible to less thorough scrutiny.

    Product Stories from the Field

    Some feedback sticks with us long after the units ship out. One group shared results from a structure-activity relationship project—late nights, tight budgets, no patience for surprises. Our lot delivered all the expected signals, minus the unclear spots that stuck out on their previous provider's NMR readouts. Another advanced a lead with our material because the consistent crystalline form let them scale efficiently from milligram to multigram screening. Our own satisfaction came from knowing expertise on the floor directly helped a distant team avoid weeks of troubleshooting and tedium.

    Over time, we’ve learned researchers often prefer our hydrochloride salt specifically so their own handling steps remain predictable. Water pick-up remains low, and the salt never turns gummy under high humidity. Subtle details like these matter less in spreadsheets and more in the daily lives of chemists juggling dozens of parallel reactions.

    Innovating Toward Sustainability and Quality Improvement

    Production quality is one piece of a broader responsibility. Chemistry, in the end, puts us at the intersection of innovation and stewardship. As pressure mounts worldwide to green organic synthesis, our team takes these challenges seriously. Several process steps for (R)-3-amino-4-(3-benzothienyl)butanoic acid hydrochloride have shifted toward less hazardous solvents and more efficiently recyclable mother liquors. Waste minimization is not a buzzword for us. By cutting down on unnecessary extractions and integrating solvent recycle, we lower both cost and environmental impact—for our site and those downstream.

    We see that auditors and external quality reviewers now want deeper information on kitting, storage, and long-term stability. That has pushed us further into regular, thorough stability screens on archived lots, even as some competitors stick with simple date-stamp expiration tactics. Our chemists keep shelf-life data, track how the hydrochloride resists hydrolysis or turns under various temperature excursions, and learn from even minor anomalies.

    Supporting Complex Pharmaceutical and Academic Projects

    Drug discovery and chemical biology projects grow more complex each year. The trend pushes every link in the supply chain to raise its game. Instead of sticking to basic supply roles, we find ourselves answering formulation questions, sharing lot-specific spectral data, and in rare but welcome cases, collaborating with creative teams to tweak handling and scaling approaches. We know some research programs have tight timelines, driven by grant cycles, corporate milestones, or even simple curiosity about a new scaffold.

    The hydrochloride form of (R)-3-amino-4-(3-benzothienyl)butanoic acid moves smoothly from early research to pilot-scale preparation work. Some teams dilute their purchasing risk by spreading orders across multiple suppliers, but we see returning customers who value our openness about process controls, root-cause analysis, and willingness to troubleshoot. Our sales reps have backgrounds in chemistry, not just business, making for smoother technical conversations and swifter problem solving.

    The Value of Scientific Rigor Over Marketing Spin

    Plenty of chemical products arrive with thick packs of documentation and claims, but over the years, we have found that true trust comes from repeated, straightforward delivery. Researchers remember if an early sample matches the commercial batch in both composition and behavior. If a plant-run lot ever drifts outside the stated chiral ratio, our internal controls catch it long before shipment. Labs depending on our material can focus on their work, bypassing time-wasting retests and unexpected deviations.

    Sometimes legacy products tempt us with a higher margin or easier synthesis route. But experience—gained from too many late-night problem solving sessions—teaches that loyalty builds over decades, not quarters. Offering a compound like (R)-3-amino-4-(3-benzothienyl)butanoic acid hydrochloride with no surprises signals to both researchers and procurement teams that manufacturing culture counts more than just logistics. That enduring connection outlasts transient pricing shifts or promotional pushes.

    Real-World Impacts and Next Steps for High-Value Intermediates

    Emerging therapeutic classes, including amino acid derivatives, pose technical puzzles with each round of process development. Our teams work openly with labs at the front line of discovery, paying close attention to their pain points. Scalability, chiral integrity, low-ash content, and minimal solvent residues—every one of these has spawned a mini-project within our manufacturing division. Our group reviews every process deviation, not just for compliance, but for lessons on how next batches might improve.

    Chiral hydrochlorides like (R)-3-amino-4-(3-benzothienyl)butanoic acid have a value twofold: direct use in synthesis and as analytical references. Because our manufacturing decisions impact not just tonnage but reputation, we keep open lines with end-users whose research might uncover new roles for this compound. By dispatching experienced staff to troubleshoot, we prevent surprises and limit failed runs—lessons earned through years of navigating scaling bottlenecks and real setbacks.

    Moving Science Forward—One Thoughtful Batch at a Time

    Manufacturing specialty chemicals never feels routine, especially for compounds living at the intersection of high-value pharma and nuanced structural chemistry. (R)-3-Amino-4-(3-benzothienyl)butanoic acid hydrochloride, synthesized on our lines, represents not just a stock number, but a history of careful decisions, rigorous checks, and real accountability.

    From our floor to research benches worldwide, every lot speaks to a collective pride built on skilled chemists, open communication, and the daily push to make every process a degree better. Long-term, the path of improvement never ends. Whether supporting CNS-active drug leads, new synthetic methodologies, or tough academic projects, we know the difference a single pure product can make. Every person here stands behind what leaves our plant, shaped not by slogans, but by results and the stories shared back from the labs that rely on our work.