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(R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol

    • Product Name (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol
    • Alias (R)-(+)-DIPPM
    • Einecs 240-322-0
    • 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

    919247

    Iupac Name (R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol
    Cas Number 127903-01-1
    Molecular Formula C17H19NO
    Molecular Weight 253.34 g/mol
    Appearance White to off-white solid
    Optical Rotation +47° (c=1, MeOH)
    Melting Point 102-105°C
    Solubility Soluble in organic solvents such as methanol and dichloromethane
    Purity Typically >98%
    Smiles C1CC(NC1)C(O)(C2=CC=CC=C2)C3=CC=CC=C3
    Inchi InChI=1S/C17H19NO/c19-17(15-10-6-2-7-11-15,16-12-8-3-9-13-16)14-18-15-5-1-4-14/h2-13,14,17,19H,1,4-5,14H2

    As an accredited (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol 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 25-gram amber glass bottle, tightly sealed, with a white label displaying the compound name, quantity, and hazard warnings.
    Shipping (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol is carefully packaged in sealed, chemical-resistant containers to ensure stability during transit. The shipment complies with all relevant regulations for laboratory chemicals, includes appropriate labeling and documentation, and is typically dispatched via accredited couriers offering priority or temperature-controlled options when necessary for safe delivery.
    Storage (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol should be stored in a tightly sealed container, protected from light and moisture. Store at room temperature, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Proper labeling and secure placement are essential to prevent accidental exposure or contamination. Follow all relevant chemical safety and handling protocols.
    Application of (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol

    Applications of (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol in Industrial Manufacturing

    As a specialized manufacturer of (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol, we supply this chiral intermediate to downstream industries where enantioselectivity and reliable process integration are essential. Extensive quality control and precise synthesis support its use in advanced applications. Below, we outline principal industrial sectors where our material serves as a key input—detailing relevant compliance frameworks, blending guidelines, role within each production process, and the resulting commercial products.

    1. Pharmaceutical Intermediate for Chiral API Synthesis

    In the pharmaceutical industry, our material acts as a critical chiral building block for synthesizing enantiomerically pure active pharmaceutical ingredients (APIs), including selective serotonin reuptake inhibitors and central nervous system agents. Controlled addition ensures the stereochemistry needed for target molecules, maintaining strict adherence to pharmacopoeial and GMP requirements throughout multistep flow or batch production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) US FDA 21 CFR Part 210/211
    • EU Pharmacopoeia monographs relevant to the target API
    • USP General Chapters for Chiral Compounds and Impurity Profiling

    Typical usage ratio

    • Added at 1.1–1.3 molar equivalents based on required API synthesis yield and enantiopurity specifications. Ratio subject to adjustment according to the downstream asymmetric synthesis pathway and reactant stoichiometry.

    Downstream process integration

    • Incorporated during chiral auxiliary attachment or catalytic asymmetric transformation phase in small-molecule API synthesis. Entered either as a starting material or advanced intermediate under controlled reaction conditions in glass-lined reactors.

    Final product types

    • Enantiomerically pure pharmaceutical actives (e.g., antidepressants, antiepileptics)
    • Chiral intermediates for further chemical modification
    • Finished dosage forms after subsequent processing and formulation

    2. Synthesis of Chiral Ligands for Catalysis

    Catalyst manufacturers employ our material to synthesize chiral ligands required for enantioselective hydrogenation and cross-coupling reactions. Such ligands establish asymmetric induction in metal-catalyzed routes, supporting large-scale manufacture of high-value fine chemicals across several chemical sectors. Consistent ligand production hinges on the purity and precise enantiomeric excess of the sourced raw material.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for catalyst and chemical production
    • REACH Regulation (EC) No 1907/2006 for substances manufactured or imported in the EU
    • Responsible Care Management System chemical safety protocols

    Typical usage ratio

    • Integrated at 0.95–1.05 equivalents relative to metal center precursor in chiral ligand synthesis. Adjustments depend on specific coordination complex formation and desired ligand properties.

    Downstream process integration

    • Introduced in the ligand-forming stage via nucleophilic addition or substitution onto metal centers (e.g., rhodium, palladium complexes) under anhydrous and inert-gas conditions to maintain stereochemical fidelity.

    Final product types

    • Chiral phosphine or amine ligands
    • Pre-catalyst formulations for asymmetric hydrogenation
    • Specialty chiral catalyst kits sold to API and agrochemical manufacturers

    3. Manufacture of Advanced Agrochemical Intermediates

    Producers of high-activity agrochemicals rely on our chiral intermediate for constructing certain enantiopure active compounds, especially fungicides and insecticides where stereochemistry affects field performance. Trace-level contaminations or racemization affect downstream efficacy and regulatory acceptance, putting a premium on input molecule quality. Rigorous monitoring at batch and in-process stages ensures compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides and Formulations
    • ISO 17025 Analytical Laboratory Quality for chiral purity validation
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products (PPP)
    • EPA 40 CFR Part 158 Data Requirements for Pesticide Registration (USA)

    Typical usage ratio

    • 0.8–1.2 equivalents based on the chemical structure and process mass intensity of desired agrochemical. The mixture is optimized according to downstream reaction efficiency and total process yield targets.

    Downstream process integration

    • Fed into the chiral step of pre-active or active ingredient synthesis by nucleophilic addition or as a resolving agent, with real-time process analytics to ensure enantiopurity.

    Final product types

    • Enantiopure fungicides and insecticides (e.g., pyrrolidinyl derivatives)
    • Chiral intermediates for further conversion into crop-specific formulations
    • Bulk technical material supplied to formulation plants

    4. Production of Analytical Reagents for Chromatographic Resolution

    Manufacturers of chiral analytical reagents incorporate our material to develop stationary phase selectors and derivatizing agents for chromatographic enantiomer analysis. The demand for reproducibility in QC labs, especially in pharmaceuticals and food safety, drives the need for consistent stereochemical properties in the supplied raw material. Rigorous input controls minimize batch variation in final standards and columns.

    Industry compliance standards

    • ISO/IEC 17025 Requirements for Testing and Calibration Laboratories
    • Pharmacopeial testing methods (e.g., USP <621> Chromatography, Ph. Eur. 2.2.46)
    • GLP (Good Laboratory Practice) where reagents are used for regulated studies

    Typical usage ratio

    • Typically 0.5–2% by weight as a functionalizing chiral selector, depending on the stationary phase matrix or derivatization chemistry. Ratio adjusted based on desired selectivity and retention characteristics.

    Downstream process integration

    • Employed during synthesis of chemically bonded or coated chiral stationary phases or as part of pre-column derivatization reagent kits, under strictly controlled reaction or blending steps to maintain selector activity.

    Final product types

    • Chiral HPLC and GC columns
    • Derivatizing reagent kits for enantiomer analysis
    • Reference standards and calibration mixtures for laboratory use

    5. Enantioselective Synthesis of Specialty Chemicals

    In R&D and pilot-scale specialty synthesis, our raw material is adopted for constructing fine chiral molecules used in chemical biology, advanced materials, and optical active auxiliaries. Industrial researchers value the precise enantiomeric control and consistent supply for iterative reaction optimization, particularly where performance and optical activity must meet design specifications.

    Industry compliance standards

    • ISO 9001 for process consistency
    • Internal analytical specifications for optical purity (>99% ee)
    • Material Safety Data Sheet (MSDS) communication per GHS

    Typical usage ratio

    • 0.2–1.5 equivalents, determined during process development depending on target molecule structure, yield maximization strategies, and economic considerations.

    Downstream process integration

    • Added in the key step of fine chemical synthesis, often involving nucleophilic addition, alkylation, or auxiliary attachment under controlled temperature and solvent conditions as validated in pilot protocols.

    Final product types

    • Chiral auxiliaries for chemical transformations
    • Optically active compounds used in advanced materials research
    • Prototype specialty products for further scale-up
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    Competitive (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol: From Synthesis to Value in Chemical Manufacturing

    Materials Built for Precision Work

    As a producer working daily with the development, optimization, and scaling of chiral molecules, I see (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol in action more than most. Years of refining batches, adjusting solvents, and repeating purifications convinced me long ago that the slightest difference in the stereochemistry of a reagent like this one can swing an entire synthesis toward success or setback. Let’s break that down for anyone evaluating materials for asymmetric synthesis, medicinal chemistry, or catalyst preparation.

    We provide the (R)-enantiomer—this matters. Its absolute configuration opens tailored routes in asymmetric reactions and chiral auxiliaries. You can see the effect best in enantioselective reduction and addition processes, where unwanted byproducts quickly creep in if the molecule isn’t pure or if the wrong enantiomer is involved. Our facility’s control over the reaction conditions, the starting raw materials, and crystallization yields keep optical purity consistent across every batch. Scrupulous attention prevents batch-to-batch variability, which users in pharmaceutical R&D and scale-up labs deeply appreciate because it keeps their data and processes reproducible.

    Structural Details & Specifications

    Batch records show that every lot of our (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol passes a chiral HPLC minimum of 99% enantiomeric excess, with residual solvent below analytical thresholds. Analytical chemists on the team run additional checks for heavy metals and trace byproducts. Keep in mind, these specifications grow out of hundreds of iterations in the plant—not abstract requirements or marketing descriptions. As far as physical state goes, our product appears as a crystalline solid, typically white to off-white depending on the minutiae of drying methods used. Melting point ranges show a slight shift based on atmospheric conditions, but process optimization has narrowed this range over the last few years through subtle tweaks in post-synthesis handling.

    Choosing crystalline over amorphous forms also means more reliable handling during weighing and transfer. Clumping, static, or smearing impacts lab prep, and observations from teams using our material feed into continued improvement. Tactile feedback from bench chemists rarely makes it into published specifications, but in practice it plays a real role in the product’s daily use in both research batches and manufacturing runs. It’s details like this, coming from people with their sleeves rolled up, that keep a material fit for its actual working environment.

    Real Uses: What the Molecule Does, and Why Manufacturers Bother

    Most of our (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol goes toward asymmetric synthesis. Its pyrrolidine ring, with dual phenyls and the alcohol handle, gives catalytic scaffolding a reputation for straightforward induction of chirality in a wide variety of target compounds. Medicinal chemists reaching for this molecule count on it to serve both as an intermediate building block (especially for psychoactive and CNS-active scaffolds) and as a ligand in small-scale catalytic applications. Having produced and shipped this compound for years, I’ve watched it play a role as both an endpoint and a stepping-stone, shifting between these roles depending on chemistry trends in the academic and pharmaceutical world.

    What draws process chemists to this compound is the handedness—it’s not just any pyrrolidinemethanol, but a specific orientation that interacts selectively within enzymes, or in metal-catalyzed transformations. Sourced with the wrong chirality, the compound may trigger a domino of failures down the development line: poor conversion, mixed product streams, extra purification steps, or outright regulatory hurdles if the target API’s required configuration goes missing. Our focus on stereochemistry isn’t academic; it’s demanded by regulations, and by the strict internal controls of scale-up teams worldwide.

    What Sets This Product Apart from Close Relatives

    There are other pyrrolidinemethanols on the market. Some buyers ask how ours stands out, and scientists on the process floor have a direct answer: robust handling, authentic chiral purity, and transparency during scale-up. Alchemizing these elements together in manufacturing only comes from day-in, day-out experience. For instance, the (S)-enantiomer will not substitute in applications keyed to the R-form. Occasionally a client compares us against racemic materials—here, they face the challenge of split product yields or laborious separation steps, both of which translate to time lost and extra cost. We minimize their risk with authentication at every lot transition. Our batch-to-batch analytical data is always available to support regulatory filings or quality assurance audits.

    Process chemists notice subtleties, whether the compound stays free-flowing or cakes up under ambient humidity, whether shipment packaging keeps light and oxygen out. We respond by refining packaging with every bit as much attention as we give the synthesis itself. Fluctuations in global logistics forced us to try new solvent exchanges and drying techniques, not just to passively meet shelf-life projections but to practically extend real-world storage. These small, practical changes don’t feature in glossy catalogs, yet they arise from feedback cycles that only a hands-on producer can manage.

    Sustainability and Change in Chemical Sourcing

    Years ago, procurement sometimes meant deciding between a handful of suppliers who shipped generic variants with traceability gaps. Production was run by the calendar, not by the end user’s needs. Today, quality standards driven by regulators, and by the high expectations of pharmaceutical, specialty, and fine chemistry clients, raise the bar constantly. Our operations grew up alongside green chemistry pressures—meaning less solvent waste, more renewable feedstock, and sectioned isolation of sensitive intermediates to reduce cross-contamination. Manufacturing practices evolve when we continuously re-invest in purification trains and solvent recovery, not just to meet but to anticipate compliance and environmental scrutiny.

    The (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol leaving our site today reflects hundreds of small improvements: safer operator handling, lower energy input, and minimized waste. Practitioners pushing for greener routes find value in a product designed downstream to leave a smaller footprint at every stage. Where alternative sources bundle in hidden costs—impurities, extra filtration, uncertain provenance—our clients return because reliability offsets apparent savings from a cheaper, less carefully produced competitor. Years of regular audits by both internal teams and third-party assessors back up those claims. Certification isn’t a box-ticking exercise; it’s woven into the checkpoints from synthesis to shipment.

    Why Tech Transfer and Regulatory Compliance Drive Our Day-to-Day Decisions

    One overlooked factor when choosing a supplier is technology transfer: can the supplier provide you not just with a product, but with full history, traceability, and technical support? As the original manufacturer, we’re on the ground with every analytical certificate, method specification, and impurity profile. Transfer to contract manufacturing, or movement into GMP production environments, places unique demands that distributors or traders simply aren’t equipped to handle. For example, our technical documentation package can extend to include validation runs of analytical methods on both our own and external chromatographic systems.

    Regulatory pressure, whether from European, American, or Asian agencies, obliges us to treat this molecule not as a commodity, but as a tightly controlled specialty reagent. We handle late-stage customization—say, special dried-down forms or custom packaging protocols—without disrupting the main production line. That flexibility, hard-earned, keeps drug pipeline projects moving without interruption. Speed counts, but depth of experience prevents short-cuts that endanger quality or compliance.

    Production Knowledge: Handling Constraints and Opportunities

    Producing (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol isn’t plug-and-play. Raw material purity, reaction kinetics, and workup protocols all invite careful supervision. Scale-up is not a matter of multiplying laboratory conditions; exothermic events, stirring rates, and even the geometry of reaction vessels factor in. My crew and I watch for signs—slight color changes, minute shifts in crystalline texture—that can signal a deviation, long before analytical equipment catches it. In the plant, tactile chemistry meets data-driven analytical support, and that balance keeps rejects rare.

    Cost pressures are real, and commodity chemicals rise and fall with global feedstock markets. With years at the plant level, I’ve seen how forward planning on sourcing phenyl and pyrrolidine starting materials shields clients from price shocks and shortages. Our purchasing policies favor long-term sustainability and backup routes, driven by the lived lessons of previous supply squeezes. Resilience means keeping paths open and keeping clients informed, not just shipping what we have on hand in hopes that it will do.

    Quality Assurance Grounded in Practice

    Our QA isn’t limited to in-process checks. Beyond finished product analytics, we track stability under transport conditions, including variable humidity and temperature profiles. A pallet delayed on a hot tarmac can compromise a month’s work, so we run degradation studies and maintain relationships with logistics partners that understand chemical sensitivity. User-level feedback cycles into shipping process enhancements, so shipped solids retain traits seen when they leave our floor.

    Packaging developments often come out of direct feedback: scientists in humid climates struggled with desiccant use or closure integrity, so we iterated packaging design to address those environmental realities. These adaptations aren’t always visible to procurement or QA officers, but in practice they shrink product loss and protect the integrity of high-value intermediates for our clients.

    Supporting R&D and Scale-Up: Beyond the Spec Sheet

    The line between small research samples and multi-kilogram development runs is more blurred than outsiders suspect. A research chemist may request a few grams to validate a synthetic route, only to ramp to kilo-scale within the quarter. We’re set up to provide consistent quality regardless of order size, with scale continuity built into both documentation and logistics. Chemists who start with our material at one stage report consistent behaviors and reactivity as their scale grows—a direct result of keeping all production in-house.

    No two R&D projects are alike. Our technical support group has handled inquiries ranging from solubility under specific solvent gradients, to impurity identification in downstream processing. Lab staff aren’t reading from abstracts—they’re the very people synthesizing or handling the material daily, sharing practical tips earned through repetition. Scaling a novel synthesis route, bringing a startup project to pilot scale, or pivoting a synthetic target often requires adaptable support; we remain closely engaged, prioritizing responsiveness and technical detail over scripted responses.

    Continuous Improvement and Customer-Centric Practice

    Real improvements happen at the boundary where manufacturing meets application. Customer feedback—from multinational pharma to niche biotech start-ups—illuminates how even a change in bottling or an adjustment in drying can change usability. Ongoing collaboration with clients prompts modifications that ripple from the factory floor to end-user success, creating a cycle where the product improves through genuine engagement and transparency.

    Our experience manufacturing (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol reinforces a belief: trust is built by tangible actions, not abstract promises or certifications. Many competitors outsource synthesis, or move between contract partners, creating hidden risk for the user. Our process sustains traceability from batch start to final delivery. Seeing the full journey from raw material to finished molecule, with each adjustment documented and justified, keeps the product consistent and reliable. This direct link to manufacture lets us stand behind every lot, ready with facts and a lived record, not just a certificate.

    Why Experience Matters for the Chemical User

    Materials produced in-house reflect a commitment rarely shared by buyers and resellers. There’s pride and accountability in watching a product persist through production, pass optimization hurdles, and reach client laboratories on time and to spec. Questions about crystal behavior, melting range shifts, or optical activity find answers rooted in familiarity: colleagues who’ve stood by the reactor, made the separation decisions, and seen the effect of real-world phenomena on yield and purity.

    Scientists seeking reliable sources for chiral auxiliaries or fine chemicals benefit when the producer takes long view, continually investing in training, equipment, and analytical support. We’ve faced urgent challenges—unexpected regulatory hurdles, acute supply shortages, and new client requirements—and prevailed by leaning on our working knowledge and a steady improvement mindset. Each new production cycle serves as an opportunity to refine, offer direct technical support, and turn theoretical improvements into functional, client-centered solutions.

    Conclusion: Commitment Beyond the Molecule

    Every gram of (R)-(+)-Alpha,Alpha-Diphenyl-2-Pyrrolidinemethanol produced at our facility carries with it a legacy of focused process optimization, attention to real-world usability, and persistent engagement with customer needs. Lab, plant, and technical support teams stand ready to share the data, experience, and detailed knowledge behind every lot, making a dependable foundation for critical research, development, or manufacturing challenges. Our approach stems from years of hands-on refinement, reflecting product quality and supplier partnership clients continually rely on.