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(R)-2-Thienylglycine

    • Product Name (R)-2-Thienylglycine
    • Alias (R)-2-thienylglycine
    • Einecs 681-427-6
    • 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

    312344

    Chemical Name (R)-2-Thienylglycine
    Cas Number 50558-36-4
    Molecular Formula C6H7NO2S
    Molecular Weight 157.19
    Appearance White to off-white solid
    Purity Typically ≥98%
    Optical Rotation [α]D20 +27° (c=1, H2O)
    Smiles N[C@H](C(=O)O)c1cccs1
    Melting Point 129-132°C
    Solubility Soluble in water
    Storage Temperature 2-8°C
    Synonyms D-2-Thienylglycine
    Inchi InChI=1S/C6H7NO2S/c7-5(6(8)9)4-2-1-3-10-4/h1-3,5H,7H2,(H,8,9)/t5-/m0/s1
    Absolute Configuration (R)-configuration

    As an accredited (R)-2-Thienylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (R)-2-Thienylglycine is packaged in a sealed amber glass bottle, labeled, 5 grams, with hazard warnings and product information.
    Shipping (R)-2-Thienylglycine is securely packaged in compliance with safety and regulatory standards for chemical transport. The shipment includes appropriate labeling, documentation, and handling instructions. It is dispatched via a certified courier, with temperature control and hazard precautions as required, ensuring timely and safe delivery to the specified destination.
    Storage (R)-2-Thienylglycine should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator temperature). Ensure the storage area is free from incompatible substances and clearly labeled. Follow all safety protocols for handling chemicals, including using appropriate personal protective equipment (PPE).
    Application of (R)-2-Thienylglycine

    Applications of (R)-2-Thienylglycine in Industrial Manufacturing

    (R)-2-Thienylglycine is a chiral amino acid derivative used by pharmaceutical, chemical, and specialty manufacturers for advanced synthesis applications. As a primary producer, we supply this compound for integration into high-value product lines in tightly regulated downstream sectors.

    1. Pharmaceutical API Intermediate for Chiral Drug Synthesis

    Global pharmaceutical companies employ (R)-2-Thienylglycine as a key intermediate for asymmetric synthesis of various chiral drug APIs, especially those targeting neurological and metabolic disorders. The compound enters enantioselective reactions, forming vital building blocks for finished drugs. Process chemists select purity grades and configure synthesis pathways based on ICH Q7 and local pharmacopoeial requirements, utilizing (R)-2-Thienylglycine to achieve strict enantiomeric excess and minimize impurities during multi-stage pharmaceutical manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • USP/NF Monograph for amino acid derivatives (where applicable)
    • EU Good Manufacturing Practice (EU GMP Part II)
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 3–10 mol% relative to target active ingredient synthesis; adjusted based on specific API’s stoichiometry and impurity profile

    Downstream process integration

    • Introduced after chiral catalyst addition in asymmetric hydrogenation or amidation steps
    • Processed under controlled temperature and inert atmosphere to ensure chiral fidelity
    • Subject to in-process QC for enantiomeric purity

    Final product types

    • Chiral drug APIs for CNS and metabolic indications
    • Specialty peptide-based pharmaceuticals
    • Prodrugs incorporating thienyl moieties
    • Clinical trial synthesis intermediates

    2. Custom Peptide Manufacturing for Research and Diagnostics

    Specialty peptide manufacturers and research reagent suppliers use (R)-2-Thienylglycine during solid-phase peptide synthesis (SPPS) to incorporate thienyl-modified, chiral amino acid residues into research peptides and diagnostic markers. Precision in integration stage and stoichiometry is critical, ensuring both sequence fidelity and the physical properties necessary for analytical and preclinical use. All peptide manufacturing processes adhere to ISO 13485 and local country standards for clinical research reagents.

    Industry compliance standards

    • ISO 13485 for medical device and research reagent QMS
    • ISO/IEC 17025 for analytical testing and QC
    • Regional regulations for diagnostic reagent purity (e.g., China NMPA, EU IVDR)
    • REACH registration where required for laboratory chemicals in Europe

    Typical usage ratio

    • 0.5–2 equivalents per peptide segment containing thienyl functionality, adjusted per chain length and substitution pattern

    Downstream process integration

    • Direct coupling via Fmoc-SPPS protocols to solid-phase resin
    • Post-coupling purification using reversed-phase HPLC
    • Component in automated peptide synthesizer feed solutions

    Final product types

    • Fluorescence-labeled research peptides
    • Immunodiagnostic calibration standards
    • Antibody epitope mimics for screening kits
    • Peptide reference materials for analytical labs

    3. Chiral Ligand and Catalyst Precursor in Fine Chemical Synthesis

    Producers of advanced catalysts employ (R)-2-Thienylglycine as a precursor for chiral ligands in enantioselective fine chemical production. The thienyl group imparts unique electronics and steric effects, making these ligands valuable in transfer hydrogenation and cross-coupling applications. The integration requires high batch-to-batch consistency and full traceability per ISO 9001 and sector-specific regulations for chemical intermediates.

    Industry compliance standards

    • ISO 9001 quality management systems
    • Responsible Care® management framework
    • REACH compliance for chemical substances in Europe
    • Local chemical control regulations (US TSCA, China IECSC)

    Typical usage ratio

    • 1–5 mol% based on target ligand backbone design and metal coordination site; adjusted for catalytic loading requirements

    Downstream process integration

    • Condensation with metal precursors under Schlenk techniques
    • Ligand derivatization in solvent-controlled synthesis reactors
    • Incorporation into catalyst test lots and screening programs

    Final product types

    • Chiral phosphine ligands for homogeneous catalysis
    • Transition metal catalyst kits
    • Chemical process R&D intermediates
    • Custom specialty chemicals with asymmetric centers

    4. Advanced Material Modifier for Electronic and Sensor Applications

    Electronic material manufacturers use (R)-2-Thienylglycine to modify polymeric and sensor substrates, enhancing charge-carrier mobility and chiral selectivity. The compound participates in co-monomer feed for functional polymers, especially in organic electronic and chemiresistor fabrication, aligning with RoHS and other material purity requirements. Formulators rely on precise mass fraction to control physicochemical characteristics in printed or spin-cast device layers.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance limitation
    • ISO 9001 for material quality management
    • IEC 61249-2-21 for halogen-free electronic components
    • REACH Annex XVII for restricted substances

    Typical usage ratio

    • 5–50 wt% within polymer blend or sensor substrate, modulated by end-use conductivity and optical property targets

    Downstream process integration

    • Mixed in pre-polymer solution prior to casting or printing
    • Integrated into microfabrication workflows under inert conditions
    • Post-processing involves annealing or photopolymerization

    Final product types

    • Conductive polymer films for flexible electronics
    • Chemiresistor sensor components
    • Printed organic transistors
    • Chiral detection layers in biosensor arrays
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    Certification & Compliance
    More Introduction

    Introducing (R)-2-Thienylglycine: Precision for Advanced Synthesis

    Meeting the Demand for Chirally Pure Intermediates

    Specialty manufacturing relies on fine-tuned building blocks. Our (R)-2-Thienylglycine stands as a chirally defined amino acid, offering chemists a repeatable pathway for asymmetric synthesis projects. Each batch stems directly from our production lines, guided by tightly monitored reaction controls and stringent isolation practices. Experience shows tangible benefits where optical purity unlocks yield and selectivity in pharma, agrochemicals, and advanced material projects.

    Reliable Identity, Consistent Output

    The chemistry behind (R)-2-Thienylglycine’s value starts with its structure: a thiophene ring bonded to an alpha-carbon bearing a carboxylic acid and an amine, both attached with (R)-configuration. The chiral center does more than label the compound; it steers reactions toward single-enantiomer outcomes. The majority of generic thienylglycine products in the market offer mixed enantiomers, muddling downstream activity or even blocking access to target molecules.

    Our product achieves enantiomeric excess exceeding 99 percent, determined by chiral chromatography and verified routinely in-house. By focusing only on the (R)-enantiomer, the headaches of separating racemates get left at the door. Decades working with fine chemical partners taught us: time invested during manufacturing replaces hours spent troubleshooting impurities. This saves more than budget lines; it can compress development time and smooth regulatory review where chiral purity plays a critical control point.

    Advantages Backed by Manufacturing Know-how

    Strictly controlled heating, solvent choice, and pH adjustments drive our (R)-2-Thienylglycine process, which eliminates inconsistent side products. Living through scale-up challenges—shift reaction volumes from grams to kilograms, wrangle heat exchange, dose chiral auxiliaries at scale—taught us to place quality over mass output. By focusing on the needs of researchers and production chemists, our workflow targets high-purity, minimal residual solvent, and a narrow melting range that simplifies further processing.

    During isolation, solid forms offer clear advantages over crude liquids. Careful crystallization and low-temperature drying methods protect against racemization or hydrolysis. Lab results are only useful if the same performance arrives drum after drum; this insight pushed us to adopt tighter batch-record standards and real-time analytical feedback, not just end-of-line spot testing. Such steady control crosses over into reliable chiral purity, low moisture, and a uniform particle profile, all backed by detailed certificates and transparent batch histories.

    The Role of (R)-2-Thienylglycine Across Industries

    Our experience supplying (R)-2-Thienylglycine spans a landscape of application demands. In pharmaceutical labs, it contributes as an intermediate for API development and custom peptide design. Chemists look for this specific stereochemistry because it enables downstream coupling with selectivity unobtainable from racemic mixtures. The thiophene ring imparts unique reactivity compared to phenyl or pyridyl analogs, letting labs explore libraries of candidates for enzyme inhibitors, ion channel modulators, and more.

    Exploration in agrochemicals highlights this compound’s versatility. Thienylglycine derivatives act as leads for bioactive agents. The (R)-enantiomer’s purity can mean higher hit rates in screening campaigns and smoother toxicology review, making scale-up less risky. As crop health research and plant protection chemistry push toward chirally pure actives, upstream consistency in building blocks like ours helps drive broader innovation.

    Material science also draws from chirality. Recent orders have gone into optoelectronic and sensor applications where enantiopure amino acids act as templates or spacers. Researchers learned that polymorph stability, surface anchoring, and device performance hinge on the fine structural differences—attributes lost with racemic raw materials or impurities.

    Distinct from Competing Options

    (R)-2-Thienylglycine outpaces generic thienylglycine offerings and racemic amino acids in three important ways. The single-enantiomer nature improves reaction predictability, especially where optical activity or single-handed selectivity matter. Comparison trials, both in our lab and with partners, reveal smoother chromatography traces, reduced by-products, and efficient peptide coupling with the (R)-enantiomer, sidestepping synthetic dead-ends found with racemic mixtures.

    Chiral purity also opens regulatory pathways. Agencies demand enantiomeric data in documentation of APIs and advanced intermediates. Our full traceability systems simplify dossier preparation and provide defense against questions of origin or batch inconsistency. Other suppliers may dilute these benefits by shifting batches through distribution chains, losing traceable links or facing re-packaging contamination. Manufacturing from source, we share direct process histories with customers, bridging the trust gap that can delay or derail projects.

    We frequently see cost-benefit tradeoffs when buyers choose generic, lower-purity, or mixed-enantiomer stock. Although sticker prices might tempt, the investment lost to extra purification, remediation, and unpredictable downstream failures outweighs any upfront savings. Our long-haul clients measure value not just by the kilo, but by lifts in yield, staff productivity, and regulatory acceptance.

    What Reliable Supply Chain Means for Researchers

    Direct shipment from our facilities ensures that handling conditions stay optimal from synthesis to customer use. Products stored at lowered temperatures in nitrogen atmosphere reduce lot-to-lot variation, even across large annual orders. We view packaging as a quality checkpoint, not a marketing shell. All containers offer clearly labelled seals, anti-tamper features, and smart labelling for full batch recognition. If a packaging format affects solubility or downstream transfer, our engineers work directly with clients to design practical solutions.

    Rapid customer feedback channels mean unexpected concerns—appearance, solubility, degradation—draw immediate technical responses, not ticket numbers. Drawing on decades spent troubleshooting for production managers and research scientists, we value prevention over apology. Detailed shipping and customs know-how from our logistics managers frequently cuts days off lead times for international delivery. For large-scale campaigns or pilot runs, staggered release and secure stock holding smoothes rollouts, avoiding costly research interruptions.

    Technical Support Anchored in Real-World Production

    Inquiries about solvent compatibility, solid-state stability, or targeted impurity profiles get real answers, drawn from hands-on process optimization. Our technical staff—seasoned in the full supply chain from bench reactions to pilot scale—collaborate openly with user teams to resolve unique process challenges. If a synthesis route stumbles, we diagnose the likely interactions using our process records, not off-the-shelf scripts, and propose alternative work-ups or purification tweaks, reinforcing our status as true manufacturing partners.

    Repeated engagement with academic and industrial users has shaped our understanding of how chiral purity impacts biological screening, process yields, and even downstream environmental impact. In cases where a partner’s method deviates from established conditions, rapid comparison trials in our labs assist in troubleshooting or scaling, with analytical data and batch reserves available for reference.

    Documented Batch Integrity and Data Transparency

    Every batch of (R)-2-Thienylglycine carries supporting analytical results: NMR, HPLC, chiral chromatogram, water content, and melting point values, all tied to unique batch numbers traceable through our digital platform. We maintain digital archives, accessible for immediate historical review, facilitating regulatory filings and inter-lab reproducibility studies. If specification limits change or a project requires higher assay, we adjust protocols in real time, giving full analytical disclosure.

    Clients once burned by mystery suppliers or silent batch shifting recognize the difference our documentation makes. We quietly back up every commercial shipment with reserves, ready for split-batch reanalysis or retrospective investigation. This level of support comes from hard-won lessons—reactor errors, raw material variability, or documentation bottlenecks cost real money and project time. We push our documentation and error-tracking higher year on year, directly in response to these field pressures.

    Environmental Awareness at Each Step

    Chemical manufacturing today responds to long-term sustainability requirements. Our processes favor high atom economy and minimize hazardous by-product generation. Recovered solvents cycle back into future batches, and in-line filtration means waste volumes drop without constant operator intervention. We track and report solvent usage, energy consumption, and emissions—not because a standard requires it, but because experience shows regulatory and customer demands rarely stay static.

    Many customers want details on green chemistry performance, including LCAs and end-of-life fates for by-products. By keeping synthetic routes tight and minimizing oxidants or heavy metal inputs, our (R)-2-Thienylglycine production supports industry moves toward cleaner supply chains. External audits welcomed annually hold us to higher standards and offer a platform for further reduction in environmental footprint. These changes tie closely to cost—wasted reagents and disposal fees disappear as processes streamline.

    Continuous Development: Scaling from Lab to Multi-Ton

    Scaling chiral molecules depends on more than reaction design; it pivots on reliability from kilogram samples through pilot vessels into multi-ton operation. Direct hands-on scale-up means every step of our (R)-2-Thienylglycine production, from raw materials to final packaging, sits under our roof. We maintain process flexibility, from exploratory academic orders to stable, repeat deliveries for pharmaceutical synthesis campaigns. Each production cycle feeds back analytical and procedural improvements, hardening protocols for the next batch.

    We learned early that theoretical yields or laboratory protocols only get so far. Practical hurdles—solubility, stirrability, heat gradients—require dedicated plant design and operator skills. Our engineers built lines that tolerate these challenges, monitored with real-time data sensors and automated feedback, preventing deviation before it damages batch output. Batch records document every step, and regular staff training keeps the team on guard for early warning signs.

    Open Collaboration: Supporting Scientific Progress

    Our partners—universities, pharmaceutical firms, agrochemical developers—see us not as a nameless source of bulk chemicals but as technical stakeholders in their innovation. Working side by side with project chemists taught us to value open exchange and impartial advice. We often participate in method development, offer gram-scale trial samples, and engage in joint troubleshooting, sharing learnings from both success and misstep.

    By offering targeted technical notes and responsive experimental data, we empower research teams to develop methods that suit their unique conditions, rather than repackage general case recommendations. If a research campaign hits a wall with off-the-shelf chiral intermediates, our process scientists engage directly with bench chemists to adjust reaction stages or purification design, bringing together the nuts-and-bolts insight of chemical manufacturing with the goals of cutting-edge discovery.

    The Trust that Comes from Direct Manufacturing

    We champion direct manufacturing. No strings attached, no confusing distribution channels. Each inquiry, order, or consultation receives the experience of decades spent shaping, scaling, and refining advanced chemicals for demanding users. Our (R)-2-Thienylglycine, shaped by customer dialog, research needs, and manufacturing trials, represents more than a box on a list: it’s a product of trust, performance, and unbroken connection between chemist and producer.

    Conclusion: Why Chemists Rely on Our (R)-2-Thienylglycine

    Projects that require (R)-2-Thienylglycine depend on purity, repeatability, and documented sourcing. We learned long ago that subpar feedstocks derail even the most promising synthesis plans. Through every challenge, from gram-scale to bulk batch, we’ve committed to providing practical, high-performing chiral building blocks. Experience, documented control, and an open technical partnership set our product—and your research—apart from the crowd. We continue to adapt, refine, and uphold not just the molecule, but the principles of responsible, data-driven chemical manufacturing.