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(R)-2-Phenyl-1-Propylamine

    • Product Name (R)-2-Phenyl-1-Propylamine
    • Alias (R)-(-)-Amphetamine
    • Einecs 629-019-8
    • 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

    418595

    Iupac Name (R)-1-phenylpropan-2-amine
    Cas Number 3886-69-9
    Molecular Formula C9H13N
    Molar Mass 135.21 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 210-212°C
    Melting Point -30°C (approximate)
    Density 0.94 g/cm³ (at 20°C)
    Solubility In Water Slightly soluble
    Optical Rotation [α]D20 +27° (c=1, ethanol)
    Chirality R-enantiomer
    Smiles C[C@H](CC1=CC=CC=C1)N
    Inchi InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m1/s1
    Synonyms (R)-α-Methylphenethylamine
    Refractive Index 1.522 (at 20°C)

    As an accredited (R)-2-Phenyl-1-Propylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled “(R)-2-Phenyl-1-Propylamine, 25 g”, with safety symbols, lot number, and tightly sealed cap.
    Shipping (R)-2-Phenyl-1-Propylamine is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It is transported according to applicable regulations for hazardous materials, typically under controlled temperature conditions. Proper labeling with hazard information and documentation ensures safe handling and compliance with local and international shipping regulations.
    Storage (R)-2-Phenyl-1-Propylamine should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep at room temperature, ideally in a cool, dry, and well-ventilated area, specifically within a designated chemical storage cabinet. Ensure proper labeling, and restrict access to trained personnel. Follow all relevant safety guidelines and local regulations.
    Application of (R)-2-Phenyl-1-Propylamine

    Applications of (R)-2-Phenyl-1-Propylamine in Industrial Manufacturing

    (R)-2-Phenyl-1-Propylamine is a chiral intermediate widely utilized in advanced chemical synthesis, particularly for the production of high-value pharmaceuticals and fine chemicals. Our manufacturing capabilities support downstream industries with stringent quality and regulatory requirements, adhering to precise process control and guaranteeing batch-to-batch consistency. Below are the main industrial application scenarios where our material contributes to end-product performance, regulatory compliance, and manufacturing efficiency.

    1. Chiral Active Pharmaceutical Ingredient (API) Synthesis

    Leading pharmaceutical producers rely on (R)-2-Phenyl-1-Propylamine as a key chiral building block for synthesizing enantiomerically pure APIs, especially those used in central nervous system (CNS) therapeutics and sympathomimetic agents. The amine’s stereospecificity contributes directly to API pharmacological profiles and meets rigorous patient safety standards. Our quality management ensures absolute enantiomeric purity and low residual solvent content for GMP manufacturing environments.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for API Production
    • European Pharmacopoeia (Ph. Eur.) specifications for chiral amines
    • United States Pharmacopeia (USP) General Chapters  <1046> for Chiral Chemistry
    • FDA 21 CFR Part 211 for Finished Pharmaceuticals

    Typical usage ratio

    • Applied at 1–3 molar equivalents per target API molecule depending on synthesis route and required yield optimization. Precise ratio determined by stoichiometric requirements and target enantiopurity parameters.

    Downstream process integration

    • Introduced during enantioselective reductive amination or alkylation steps; often forms the core of asymmetric catalytic reactions or crystallization-based resolution. In some processes, direct coupling to protected intermediates under anhydrous conditions is necessary for purity assurance.

    Final product types

    • Enantiopure CNS stimulant APIs
    • Chiral amine analogs utilized in anti-obesity or antidepressant drug products
    • Sympathomimetic drug substances

    2. Synthesis of Agrochemical Intermediates

    Agricultural chemistry companies adopt (R)-2-Phenyl-1-Propylamine in the stepwise preparation of chiral intermediates for crop protection agents, notably certain classes of selective herbicides and insecticides where enantioselectivity influences biological activity and environmental behavior. Process reliability and traceability back to the raw amine assure long-term supply compliance for multinational agrochemical producers.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Intermediates
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001 Quality Management Systems
    • REACH Annex VII–X for chemical safety documentation

    Typical usage ratio

    • Generally included at 0.5–2 mol equivalents per target intermediate, with precise addition tailored for desired enantiomeric excess and downstream yield requirements.

    Downstream process integration

    • Used during enantioselective amination or amidation reactions within multi-stage synthetic routes. Often incorporated via catalytic hydrogenation or C–N bond formation when preparing key intermediate scaffolds.

    Final product types

    • Chiral herbicide precursors such as phenoxyalkanoic acid derivatives
    • Intermediates for pyrethroid or neonicotinoid insecticides
    • Fine chemical intermediates required for next-generation crop protection compounds

    3. Fine Chemical Synthesis for Fragrances and Flavors

    Specialty chemical producers engaged in the synthesis of high-value fragrance and flavor molecules integrate (R)-2-Phenyl-1-Propylamine as a chiral intermediate for esterification or further amide synthesis. Its controlled stereo-chemistry enables the creation of aroma compounds with enhanced olfactory impact or regulatory-accepted chiral signatures.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Regulation (EC) No 1334/2008 for Flavourings
    • ISO 9001:2015 for fine chemical manufacturing
    • FEMA GRAS listing procedures for food-grade aroma chemicals

    Typical usage ratio

    • Typically 0.2–1.5% w/w in batch reactant mixtures, adjusted according to target compound stereochemistry and aroma intensity specifications.

    Downstream process integration

    • Entered at the chiral amination or amidation stage; frequently used in the controlled formation of enantiopure alcohols or esters through subsequent reduction, hydrolysis, or Fischer esterification.

    Final product types

    • Chiral fragrance building blocks
    • Flavour precursors for essential oils
    • Fine perfumes and food-grade aroma molecules

    4. Optical Resolution and Chiral Ligand Precursor Manufacturing

    Chemical manufacturers specializing in asymmetric catalysis utilize (R)-2-Phenyl-1-Propylamine for preparing chiral ligands and resolving agents. Its enantiomeric excess, traceability, and controllable impurity profile underpin catalyst batch reproducibility and chemoselectivity for both in-house and custom catalyst solution suppliers.

    Industry compliance standards

    • Chemical Abstracts Service (CAS) batch registration
    • ISO 17034:2016 for Reference Material Producers
    • GLP (Good Laboratory Practice) for ligand synthesis batches
    • Internal quality control protocols for chiral reference materials

    Typical usage ratio

    • Typically 1 molar equivalent per target chiral ligand or resolving agent; excess may be used for maximizing recovery in resolution protocols, depending on the scale of batch operations.

    Downstream process integration

    • Employed during the condensation or chelation with transition metal salts, typically introduced under inert atmosphere for reproducible chiral ligand formation; also used in salt formation with racemic substrates during chiral resolution workflows.

    Final product types

    • Chiral diphosphine ligands for asymmetric hydrogenation
    • Resolving agents for laboratory-scale enantiomer separation
    • Reference-grade chiral standards employed in analytical QC
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    Certification & Compliance
    More Introduction

    Introducing (R)-2-Phenyl-1-Propylamine: Our Perspective as the Manufacturer

    Our Story with (R)-2-Phenyl-1-Propylamine

    We have worked with countless amines in our production lines, and among them, (R)-2-Phenyl-1-Propylamine stands out due to its chiral purity and specific uses in advanced synthesis. In the world of chiral building blocks, consistent optical activity often makes or breaks a process. Observing demand change over the years, our team has focused on process refinement for this compound, always aiming to deliver material that supports both research and industrial innovation.

    Through years of direct experience, we've observed the growing need for (R)-2-Phenyl-1-Propylamine as a chiral intermediate. It earns its keep in pharmaceutical R&D labs and pilot plants alike. Its molecular configuration is a magnet for chemists seeking selectivity in final products. Taking that requirement seriously, we've adjusted our production steps, analytical controls, and purification techniques. We maintain a focus on reproducibility, paying close attention to chiral integrity from the raw materials through to the packaged amine.

    The Molecule in Detail

    (R)-2-Phenyl-1-Propylamine—also known in various literature as (R)-α-methylbenzylamine—embodies specificity. Its structure gives it a unique edge over its racemic or (S)-enantiomer counterparts. With a chiral center next to the amine, it brings both enantioselectivity and reactivity to the table. The specifications most clients discuss with us involve high enantiomeric excess, single-digit moisture content, and LC or GC traceability for by-products. We've set up our QC lab to handle these demands, running chiral HPLC as a baseline, so every batch offers the profile synthetic chemists require.

    Our batches typically come as a colorless to pale yellow liquid, with a faint but distinct aroma familiar to those who have handled other aralkylamines. It dissolves well in common organic solvents such as ether or dichloromethane, and it blends into reactions without the hassle of slow dissolution or phase separation. In our synthesis halls, this makes scale-up far simpler, especially for clients running continuous-flow chemistry or those transferring benchwork to pilot-scale reactors.

    Direct Experiences with End-Use Cases

    Many of our regular customers come from the pharmaceutical world, especially those working on active pharmaceutical ingredient (API) intermediates or new ligand architectures. In small-molecule synthesis, it's often the case that (R)-2-Phenyl-1-Propylamine serves as a backbone in asymmetric transformations. We've answered requests from chemists needing high-purity material for reductive amination, boronation, or as an organocatalyst starter. It is rewarding to see this amine provide the selective advantage over achiral amines in enantioselective synthesis.

    Some clients approach us to discuss the difference between our (R)-2-Phenyl-1-Propylamine and generic options from bulk suppliers. The usual shortfalls they mention—variable optical purity, unpredictable impurity levels, or trouble scaling from gram to kilogram—are ones we fix by controlling every production step. We regularly collaborate with R&D departments, giving technical advice about solvent compatibility, downstream purification, and optimal storage. Over the past decade, we have helped teams save months that could have been lost to rework or troubleshooting by providing direct feedback and hands-on technical support.

    Comparing Quality: What Matters in Practice

    One common area of confusion involves the subtle but critical differences that chiral amines like (R)-2-Phenyl-1-Propylamine introduce to multi-step synthesis. This molecule is not interchangeable with racemic forms, despite similarities in bulk properties. Using the wrong enantiomer can result in reduced activity or even failed reactions in later steps, leading to costly delays. Our production managers have long focused on minimizing cross-contamination and racemization at every stage. Temperature control, catalyst choices, and non-aqueous handling play a major role, and by being manufacturers, not resellers, we manage every aspect of this careful work ourselves.

    A good portion of our customer base is deeply familiar with the cost of product recalls or regulatory setbacks caused by poor traceability. That has shaped our commitment to documenting every batch at each stage, not relying on third-party testing alone. Client audits in our plant have made it clear—labs want more than a certificate of analysis; they want to see the methods, the raw data, and the controls in action. Our openness in this area has won us long-standing partnerships, not just transactions.

    Process Upgrades & Continuous Improvement

    The global landscape for chiral chemicals has changed. Demand for higher purities, environmental sensitivities, and tighter specifications have pushed us to evolve. We have invested in up-to-date technologies like solid-phase purification and in-line analysis. This offers us clear advantages in tracking product quality before, during, and after the core synthetic steps. By working directly with feedback from application scientists, we’ve learned which properties matter most and have shaped our manufacturing process accordingly.

    Energy efficiency and environmental compliance cannot be an afterthought. Regulatory trends in the last several years now drive manufacturers to cut solvent waste and use greener reagents. In our plant, we've shifted key steps from high-volume solvent washes to more targeted, closed-system extractions. Not only does this help laboratories meet their environmental commitments, it also preserves product integrity. We routinely share our solvent optimization data with partners, so their entire supply chain operates with fewer hiccups.

    As with any specialty chemical, safeguarding against contamination and cross product interference makes or breaks the commercial value. Our approach to safety integrates strict segregations of workspaces, closed reaction vessels, and documented cleaning cycles between shift changes. This ensures that each liter of (R)-2-Phenyl-1-Propylamine delivers the purity, optical rotation, and by-product profile customers expect.

    Supporting Clients & Custom Needs

    While catalogs and stock lists have their place, custom synthesis has always been a strong suit for our site. We've responded to requests for special packaging, unusual concentrations, or integration of in-process analytical samples sent straight to client labs for pre-shipment verification. In research environments, every project comes with unique requirements. Being the manufacturer, we can quickly adjust a batch schedule or modify purification steps, cutting weeks off expected lead times. We see every client conversation as a two-way process. Technical teams send us feedback, which we use to adjust future runs, so the final product aligns closer with end-use needs.

    Our technical staff often gets called into detailed discussions—how will a slight adjustment in basicity affect downstream cyclizations, or can alternative drying reagents make a difference for a chromatographic separation? By maintaining direct lines between production chemists and clients, small questions get fast answers grounded in actual plant knowledge. This responsiveness protects projects from setbacks and lets clients move forward in their synthesis work with fewer surprises.

    Meeting New Standards

    Rising standards in both regulatory and technical fields continue to influence the way we handle (R)-2-Phenyl-1-Propylamine. The industry now sets the bar higher, especially for products destined for regulated markets or sensitive research environments. Documents such as batch history, validation of analytical methods, and even environmental traceability become non-negotiable parts of our operation. We recognize that compliance is not a bureaucracy to skirt; it’s a baseline expectation from serious partners. Our audits are open, our data are up for inspection, and we invest in regular staff training so nobody gets caught behind on evolving standards.

    Some requests call for full breakdowns of impurity spectra, including trace solvents, chiral purity, and batch-to-batch reproducibility over long production runs. For this, we rely on both in-house analytics and access to third-party verification when requested. We don’t hide methodologies or limit communication when a client wants details on a lot. Instead, we share SOPs, analytical reports, and even offer remote or on-site inspections. Over time, this approach brings a higher level of trust and has made our (R)-2-Phenyl-1-Propylamine a preferred choice for labs pushing the envelope on new drug entities.

    Perspectives from Our Team

    Our engineers and chemists can recount the many lessons learned during process optimization. For instance, minor shifts in pH during recrystallization have outsized effects on enantiomeric excess. Simple procedural steps—like using nitrogen blanketing or cooling bromide additions just a bit slower—have resulted in better consistency. Sharing those findings with clients has leveled up many downstream projects and reduced the frustration that comes with trial-and-error sourcing.

    A few years back, a partner came to us with trouble sourcing consistent chiral amines for scale-up drug synthesis. Off-the-shelf materials from large distributors landed them with failed pilot batches, delayed filings, and a mounting cost. We met their team, ran side-by-side lots with altered conditions, and traced the problem back to batch instability in the original supplier’s route. By switching to our high-purity (R)-2-Phenyl-1-Propylamine, the team hit their milestones and slashed both delays and rework costs. Drawing on real experiences like this, we believe the manufacturer’s full engagement adds far more value than any anonymous middleman could.

    Global Reach, Local Sensitivity

    We interact with clients facing a wide scope of regulatory pressures, climatic conditions, and local preferences in handling chemical shipments. Our logistics network responds by providing reliable lead times, flexible shipping, and solutions for temperature-sensitive cargo. Customs clearance, dangerous goods compliance, and real-time tracking are all managed in-house to protect the product and keep timelines. By keeping logistics direct, we reduce the chance of mishaps, lost time, and degraded samples—a reality well-understood by anyone ever forced to discard a valuable delivery due to improper handling.

    As supply chain security becomes a hot-button issue, the real manufacturer’s supporting documents provide an audit trail that cannot be forged. Clients need confidence in every drum delivered, especially if their own auditors or those of regulatory agencies will check its origin and journey. We provide that with digital batch logs, hand-signed transfer documentation, and open channels for post-delivery support. From day one, our supply agreements reflect each partner’s needs, not a one-size-fits-all printout. Local support staff get involved, so guidance is practical and grounded in actual experience—not just phone scripts or form emails.

    From R&D to Full Production

    The journey from milligram-scale feasibility studies to full production is rarely straightforward. As an active manufacturer, we routinely walk alongside clients from bench-top experiments to industrial campaigns. By scaling our (R)-2-Phenyl-1-Propylamine production between research, pilot, and commercial quantities, we allow seamless transition for clients ramping up output. Often, clients bring us in at the earliest stages, inviting feasibility discussions and requesting help solving problems tied to material consistency, stability, or safety in handling.

    Our team also supports technology transfers, both locally and internationally, providing documentation, samples, and training directly onsite or through digital communication. Many times, the specific way (R)-2-Phenyl-1-Propylamine performs in a reaction—its solubility, rate of addition, or reactivity with other substrates—can change as the scale grows. With technical production insight at every phase, scale-ups rarely bring surprises, and if they do, the troubleshooting happens in real time.

    Continuous Focus on Quality & Improvement

    Quality does not stand still. Every production batch is scrutinized under our validated processes, but we stay open to new techniques, feedback, and changes in the field. Regulatory changes, such as restrictions on hazardous solvents or extended shelf-life requirements, often drive us to change working parameters midstream. Technicians attend workshops, run comparative studies, and trial new analytical methods on test runs before they become routine. In the last cycle alone, a new approach to solvent exchange improved final material color and minimized post-reaction cleaning cycles, freeing up capacity for shorter lead times.

    Mistakes are not swept under the rug; they become fuel for better controls. On occasions when a shipment required rework or a client reported an off-spec smell in a new batch, we traced every step to catch root causes and issued full, documented resolutions. Over time, these honest adjustments have cemented trust with every long-term partner, giving them certainty that feedback is received, considered, and integrated back into production lines. This cycle of correction and improvement keeps our output consistent and future-proofs us against compliance drift.

    A Standout Choice in Chiral Amines

    Years in the manufacturing trenches have taught us that supply quality means more than lab reports. It speaks to the entire cycle—sourcing, synthesis, purification, logistics, and follow-up. For (R)-2-Phenyl-1-Propylamine, beyond its chemistry, it’s the way we produce and support the product that speaks to why clients return. Chemists, project managers, and regulatory staff alike need direct, transparent support. Our approach to every drum, from hundred-gram research packs to multi-kilogram industrial shipments, reflects the reality that chiral integrity and documentation shape both results and reputations.

    By handling all aspects internally, we make sure every batch aligns with the standard our clients rely on. From regular updates on process improvements, to open doors for audits and transparent records, our aim has always been to be more than just a source of chemicals—to act as an engaged, practical, and informed partner in every synthesis journey involving (R)-2-Phenyl-1-Propylamine. This ongoing investment in process, people, and partnership defines our place in the chiral amine market and serves as our best answer to the shifting needs of scientific and industrial advancement.