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(1R,2R)-(+)-1,2-Diphenylethylenediamine

    • Product Name (1R,2R)-(+)-1,2-Diphenylethylenediamine
    • Alias DPEN
    • Einecs 224-857-2
    • 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
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    Specifications

    HS Code

    595455

    Iupac Name (1R,2R)-1,2-diphenylethane-1,2-diamine
    Cas Number 5397-45-1
    Molecular Formula C14H16N2
    Molecular Weight 212.29
    Appearance White to off-white crystalline solid
    Melting Point 124-126 °C
    Optical Rotation [α]D20 +86° (c=1.0, EtOH)
    Solubility In Water Slightly soluble
    Boiling Point 393.3 °C at 760 mmHg
    Density 1.09 g/cm³
    Purity Typically ≥98%
    Synonyms trans-(+)-1,2-Diphenylethylenediamine; (+)-DPEN
    Storage Conditions Store at 2-8 °C, protect from light and moisture

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

    Packing & Storage
    Packing The 25g amber glass bottle features a white screw cap, displaying a white label with product name, quantity, chemical structure, and hazard symbols.
    Shipping (1R,2R)-(+)-1,2-Diphenylethylenediamine is shipped in tightly sealed containers, protected from light and moisture. It is handled according to standard chemical safety protocols, with appropriate labeling. The package complies with all relevant regulations for chemical transport, ensuring safety and integrity during transit to prevent contamination or accidental exposure.
    Storage (1R,2R)-(+)-1,2-Diphenylethylenediamine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Store at room temperature and ensure the area is designated for chemical storage, following all applicable safety protocols and local regulations.
    Application of (1R,2R)-(+)-1,2-Diphenylethylenediamine

    Applications of (1R,2R)-(+)-1,2-Diphenylethylenediamine in Industrial Manufacturing

    (1R,2R)-(+)-1,2-Diphenylethylenediamine is a high-purity chiral diamine widely used in asymmetric catalysis, pharmaceutical intermediate synthesis, ligand preparation for specialty catalysis, and organic material modification. As a direct manufacturer, we supply this compound to customers requiring reliable chiral control and strict quality standards for downstream production.

    1. Asymmetric Hydrogenation Catalysts for Pharmaceuticals

    This material serves as a primary chiral ligand in the manufacturing of transition metal catalysts, particularly for asymmetric hydrogenation processes within the pharmaceutical industry. Its stereochemistry enables precise control over enantioselective reduction of intermediates, supporting production of active pharmaceutical ingredients (APIs) like chiral amines and alcohols at industrial scale. Pharmaceutical manufacturers use this diamine to optimize the selectivity and yield of hydrogenation reactions, integrating it into their cGMP-compliant production lines.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP Pharmacopoeia guidelines for residual metals
    • 21 CFR Part 211 (FDA, finished pharmaceuticals)
    • EMA Guideline on the Sterilization of APIs

    Typical usage ratio

    • 0.5–2.5 mol% relative to metal catalyst, adjusted by substrate complexity and target yield

    Downstream process integration

    • Introduced during catalyst preparation phase, complexed with rhodium or ruthenium salts prior to substrate dosing
    • Purified from reaction mixture using phase separation or chromatography, depending on scale

    Final product types

    • Enantiomerically enriched chiral secondary amines
    • Chiral beta-amino alcohols
    • Active pharmaceutical ingredients with strict enantiomeric excess specifications

    2. Ligand for Metal-Catalyzed Fine Chemical Synthesis

    Our customers engaged in specialty fine chemical synthesis utilize this diamine as a chiral ligand for constructing metal complexes, especially for cross-coupling and addition reactions in the synthesis of advanced intermediates. The stereoselective environment created by this ligand facilitates the production of intermediates that meet precise downstream purity and configuration standards for electronics, agrochemicals, and performance chemicals.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH registration and SVHC compliance (EU)
    • Substance Volume Tracking (SIEF, EU REACH)
    • EPA TSCA Inventory (U.S.)

    Typical usage ratio

    • 1–7 mol% compared to catalytic metal; varies by batch size and target yield

    Downstream process integration

    • Complexed in situ with palladium or nickel during catalyst charging
    • Added pre- or post-solvent charging based on reaction protocol and solvent characteristics

    Final product types

    • Chiral building blocks for OLED and liquid crystal displays
    • Agricultural intermediate compounds
    • Custom intermediates for photoinitiators and thermal curing agents

    3. Chiral Auxiliary in Agrochemical Active Ingredient Synthesis

    Manufacturers of agrochemical actives use (1R,2R)-(+)-1,2-Diphenylethylenediamine as a chiral auxiliary to induce stereoselectivity in cyclization or addition reactions, supporting the scalable production of high-purity crop protection agents. The auxiliary remains robust during large-scale processing, allowing for its recovery and reuse when necessary.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 17025 Accredited Laboratory Testing
    • FAO/WHO specifications for pesticides

    Typical usage ratio

    • 10–25 mol% relative to main substrate, adjusted to match target enantioselectivity and cost-control strategies

    Downstream process integration

    • Added before substrate introduction in batch reactors, often with base and solvent to form the chiral intermediate
    • Isolates via crystallization for removal after target product formation

    Final product types

    • Enantiopure herbicide active ingredients
    • Selective fungicide intermediates
    • Chiral insecticide actives

    4. Building Block for Organocatalyst Synthesis

    This diamine acts as a primary precursor in manufacturing second-generation chiral organocatalysts, significantly used in specialty polymer production and advanced material science research. The material’s configuration affects catalytic activity and selectivity in downstream polymerizations and stereoselective transformations required for high-performance applications.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • GLP (Good Laboratory Practice) for process validation
    • RoHS for electronics applications (if used in display or sensor industries)
    • Chemical Control Law (Japan, if exported)

    Typical usage ratio

    • Varies from 3–15 mol% per polymerizable monomer group, based on target catalyst efficiency and molecular weight control

    Downstream process integration

    • Functionalized with aldehydes or ketones during catalyst precursor stage
    • Fed into continuous or semi-batch reactors for catalyst assembly and performance testing

    Final product types

    • Chiral organocatalysts for specialty polymerizations
    • Polymeric materials for advanced coatings
    • Custom chiral reagents for downstream research and electronics
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    Competitive (1R,2R)-(+)-1,2-Diphenylethylenediamine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (1R,2R)-(+)-1,2-Diphenylethylenediamine: The Backbone of Precision Synthesis

    Meeting the Need for Reliable Chiral Building Blocks

    Out on the production floor, (1R,2R)-(+)-1,2-Diphenylethylenediamine stands apart for its clarity and consistency. Over the years, chemists searching for reliable chiral diamines have often arrived at our door, looking for high optical purity from the source. We prepare this diamine in batches that consistently reach optical purities above 99%, and our in-house analytical team uses HPLC and polarimetry to confirm every lot. A quick glance at the white crystalline powder can’t reveal much; the real difference only becomes clear in downstream application, whether as a ligand in asymmetric catalysis or a key intermediate headed for a pharmaceutical backbone.

    Model and Specifications Built for Demanding Users

    Each lot carries its batch number, our own guarantee of traceability and transparency. We keep moisture low—less than 0.2%—and residual solvent meticulously below industry-accepted marks, as GC and Karl Fischer titration confirm. Through continual investment in process control, from raw material sourcing to final packaging, we minimized racemization and possible contamination. Our packing process keeps material dry and stable, from the production vessel to the final glass bottle. Clients often ask about micronization; we offer standard mesh but will adjust particle size on request, always aware of how even granularity can affect reactivity in certain applications.

    Purpose-Built for Asymmetric Synthesis and Catalysis

    On the bench, (1R,2R)-(+)-1,2-Diphenylethylenediamine works as a powerful ligand for substrates that demand high stereochemical control. Many have cited it as their go-to choice for the Sharpless asymmetric aminohydroxylation and dihydroxylation reactions, and our team has worked directly with process chemists tailoring this diamine for large-scale catalysis. We've seen a gradual shift from racemic mixtures to enantiopure variants, tracing this movement alongside expanding GMP standards and regulatory oversight. Our R&D process keeps step, running impurity profiles and long-term stability tests to ensure that our material consistently serves in both academic labs and industrial reactors.

    Real Differences from Other Available Options

    Many manufacturers approach ethylenediamine derivatives by resolution or from a chiral pool. We have favored asymmetric synthesis routes, taking greater control of stereochemistry, and find this pays off for clients sensitive to minor-waste chiral impurities. Cheaper alternatives, often imported with few controls or repackaged through multiple hands, usually provide less than full analytical data. Over time, our repeat customers tell us they see fewer batch-to-batch variations—this means less troubleshooting, more reliable yields, and more trust in their process validation steps.

    From Bench to Bulk Scale: Addressing Scale-Up Challenges

    Feedback from users routinely drives improvements in our workflow. We have seen clients struggle during scale-up, when poor heat transfer or insufficient mixing in larger vessels can introduce local overheating and drift optical purity. To tackle such issues, we maintain pilot reactors that simulate end-user conditions, not just milligram flasks. Our scale-up chemists optimize exothermicity and flow, ensure uniform mixing, and profile side-products likely to arise at scale. For clients with unique isolation needs, we have adjusted crystallization conditions, supplying custom solvate-free lots or pre-dried powders, so that process chemists can skip an extra drying or washing step.

    Understanding Purity Beyond the Numbers

    Purity, for us, means not just a clean HPLC trace, but confidence in absence of both inorganic and organic micro-impurities. Each run includes checks for residual metals and trace amines, as catalyst carryover can disable sensitive downstream reactions. Our longstanding partnerships with pharmaceutical groups force our hand to hold thresholds stricter than typical commodity producers. The best labs look beyond the certificate and want details on every data point, so we keep an archive of full batch records and can share extra chromatograms or spectral data on request. We've run comparative trials—with both our product and samples sourced elsewhere—documenting improved reproducibility in stereochemical outcomes.

    Beyond the Bottle: Safety in the Real World

    Daily handling of chiral diamines like (1R,2R)-(+)-1,2-Diphenylethylenediamine is routine in our facility, but we extend this attention out to our clients. Training for correct handling and PPE, proper containment during solid transfer, and real communication on potential exposure hazards forms the foundation of our long-term safety record. While the material has a moderate base strength and can release ammonia on decomposition, we built containment and neutralization into our plant operations—a lesson drawn from early pilot-scale mishaps. Data sheets and guidance for accident response come directly from decades seeing these issues develop, not just copied standards. We urge end users to store the compound cool and dry, and many have adopted our suggestion of using inert gas overlays for long-term storage, limiting oxidation and extending shelf life.

    Supporting Synthesis Under Regulatory Scrutiny

    In the last decade, growing demands from pharmaceutical oversight—FDA, EMA, and others—have pushed many chemists to audit their sources ever more carefully. Because chiral diamines can end up in intermediates for APIs or as ligands for metal catalyzed routes that end in a drug molecule, every step must stand up to scrutiny. Full traceability from lot to lot, with documentation attesting to our in-house controls, reduces regulatory risk for our customers. Audits—scheduled and unscheduled—have pushed us to invest more in batch documentation and in regular requalification. This transparency carries forward into our willingness to provide process data and to adapt production to changing monograph expectations or to furnish unrestricted DMFs for regulatory review.

    Productivity in the Lab, Reliability in Industry

    We built our reputation not on clever advertising but on shipments that matched sample quality, with reorder rates pushing above 90%. Process chemists provide feedback on how well the diamine dissolves, how predictable its melting point remains, how little dusting occurs in bulk charging. Material that clumps in storage or picks up moisture at the bench can mean distraction and rework. The crystal habit and solid form play a real role in efficiency, and we’ve adjusted drying protocols through years of direct dialogue. Supply assurance matters just as much; we keep a deep safety stock buffered in our own controlled rooms, so that unpredictable delays or surges in demand do not interrupt our client workflows.

    Toward Greener Manufacturing

    Each kilogram of (1R,2R)-(+)-1,2-Diphenylethylenediamine previously required significant solvent, but we've overhauled our workup process to use greener solvents and minimize chlorinated waste. Recycle and reuse loops save on both cost and downstream disposal, while onsite recovery prevents unnecessary incineration. We share LC/MS profiles with our clients who value green chemistry claims, supporting validation of residual solvent content and batch-specific waste minimization. Ongoing improvement means regular revalidation of starting material suppliers; we avoid cost-cutting on starting materials that can leave hidden impurities, supporting our belief in responsible sourcing.

    Working with the Community of Users

    University labs, startups, and multinational manufacturers all use our diamine, but each brings different expectations. Method transfer support, from technical advice on solution preparation to direct troubleshooting in non-standard reactions, sets us apart. Several academic groups have published with material sourced from our lots, confirming findings with our detailed NMR and chiral HPLC data. Industry chemists often need bulk, but also continuity—a guarantee that what arrives next quarter matches what landed today. The team here commits to technical backup, not just dispatching a product but answering “why this lot runs better” or “how this crystal form dissolves at scale.”

    Continuous Innovation in Chiral Diamine Supply

    Chiral diamines such as (1R,2R)-(+)-1,2-Diphenylethylenediamine have become a critical go-to for natural product synthesis, drug development, and fine chemical research due to their ability to impart stereochemistry. The push for even higher selectivity has brought new requests for custom analogues; we now develop derivatives with specialist groups, modifying aryl groups or introducing protective groups to fit unique project needs, always drawing directly from our base synthetic expertise. As new metallic catalytic systems emerge, we mimic customer setups to validate performance in real-world conditions, running head-to-head comparisons and feeding back recommendations for best practice.

    Addressing the Hidden Issues in Scale and Consistency

    One issue not often discussed is the hidden challenge of blending lots or switching between suppliers mid-project. We have seen chromatographic drift, changes in dissolution rates, or subtle shifts in melting point—often due to micro-impurities or slight differences in synthetic route. By keeping in-house production from start to finish, we stop these “hidden hand” effects, so developers can keep process variables tight. Analytical support for batch comparability across multiple runs ensures every pilot campaign flows smoothly to full-scale production. Our engineers run periodic requalification, catching early shifts from reactor fouling or solvent drift.

    Transparent Collaboration Through Every Purchase

    We do not just list products; we provide collaboration. End users often need pre-shipment samples, access to full analytical records, or side-by-side performance data for regulatory documentation. Our technical support does not disappear after shipment—questions about solubility, recrystallization, and pre-treatment all feed back into production improvements. By maintaining direct dialogue and quick-response support, we ensure even custom or urgent requests, such as low-dusting grades or pre-milled powders, fit right into user processes without pause.

    Mistakes as Opportunities for Progress

    Early in our production history, a single uncontrolled exotherm during scale-up nearly doomed an entire batch, prompting new investment in temperature control and real-time monitoring. Critiques from dissatisfied project chemists—surprised by a higher than expected baseline area in HPLC traces—drove our push for cleaner isolation. Adapting quickly to such feedback has meant fewer recurring errors and faster achievement of industry benchmarks. We document every deviation, studying not just numbers but root causes, continually optimizing to match or exceed global standards. Quality is not a checklist but an ongoing push for better solutions.

    Long-Term Supply Commitment

    Global logistics disruptions revealed weaknesses in fragmented supply chains, with interruptions or inconsistent product quality. By keeping synthesis, purification, and packaging under direct control, we shield our partners from these variables. Equally, we always align production scheduling with forecasted demand, but leave enough flexibility to absorb urgent upticks. Real-time inventory systems, paired with direct-to-user distribution, mean orders ship from controlled stock, not forgotten third-party warehouses. This commitment resonates with process chemists—every gram they weigh comes with confidence in a tightly integrated supply network.

    As the Synthesis Landscape Shifts

    Chiral chemistry rapidly evolves, demanding speed and responsiveness from material suppliers. As new methodologies appear, we adapt processes, qualifying new grades or developing ready-to-use blends specific to major applications. We actively gather end-user feedback on function in novel transformations, not just established ones. Such dialogue drives future modifications—such as particle size changes or solvent optimization—in our next-generation offerings. Staying agile in production and open to continuous feedback keeps us aligned with leading research and industrial trends.

    Raising the Standard for Chiral Diamine Quality

    For us, (1R,2R)-(+)-1,2-Diphenylethylenediamine represents more than a line item; it’s a reflection of our focus on rigor, transparency, and direct user support. Our ability to control everything from initial synthesis to final shipment means each batch arrives consistent, traceable, and fit for use in the most demanding applications. We treat each feedback, question, or challenge as an invitation to deepen our expertise, improve our process, and provide even better support to our long-term partners.