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2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde

    • Product Name 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde
    • Alias Benzyloxypropylhydrazinecarboxaldehyde
    • Einecs 846-910-1
    • 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

    269400

    Iupac Name 2-[(1S,2S)-1-ethyl-2-(phenylmethoxy)propyl]hydrazinecarboxaldehyde
    Molecular Formula C13H20N2O2
    Molecular Weight 236.31 g/mol
    Smiles CC[C@@H](COC1=CC=CC=C1)[C@@H](N)C=O
    Inchi InChI=1S/C13H20N2O2/c1-2-11(13(15)16)12(14)17-10-9-7-5-3-4-6-8-9/h3-8,11-12H,2,10,14H2,1H3,(H,15,16)/t11-,12-/m0/s1

    As an accredited 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 10 grams, with tamper-evident seal, labeled with chemical name, hazard warnings, batch number, and storage instructions.
    Shipping This chemical, 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde, ships in compliance with all relevant safety regulations. It is typically transported in sealed, appropriately labeled containers, with cushioning to prevent breakage. Shipping methods may require temperature control and documentation of hazardous material handling, depending on the quantity and destination requirements.
    Storage Store 2-[(1S,2S)-1-Ethyl-2-(phenylmethoxy)propyl]hydrazinecarboxaldehyde in a tightly sealed container, protected from light and moisture, at 2–8 °C (refrigerator). Keep away from strong acids, bases, oxidizing agents, and sources of ignition. Store in a well-ventilated, dry area. Clearly label the container and ensure only trained personnel handle the substance using appropriate personal protective equipment (PPE).
    Application of 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde

    Applications of 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde in Industrial Manufacturing

    This advanced hydrazinecarboxaldehyde derivative is widely used in regulated pharmaceutical synthesis, agrochemical intermediates, specialty polymer manufacturing, and advanced organic synthesis for research and commercial production. Below, we present selected application scenarios that reflect the current industrial demand and compliance requirements for this chemical ingredient across critical supply chains.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Our hydrazinecarboxaldehyde derivative serves as a key protected intermediate for certain chiral hydrazine-based active molecules. The compound is used in the controlled condensation and reduction steps for manufacturing specialized antihypertensive agents and CNS-targeted drugs. Downstream pharmaceutical companies value the product’s enantiomeric purity and stability during multi-step organic synthesis performed under cGMP protocols.

    Industry compliance standards

    • 21 CFR Parts 210/211 (US FDA cGMP requirements)
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. Monographs for intermediate purity
    • USP/NF API precursor guidance (when applicable)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to target substrate per reaction batch
    • Adjusted based on process yield and enantiopurity specifications

    Downstream process integration

    • Used after initial substrate activation, before final deprotection and crystallization steps
    • Introduced in closed reactor trains compliant with GMP cleaning validation

    Final product types

    • API intermediates for antihypertensive compounds
    • Building blocks for CNS pharmaceutical agents
    • Enantiomerically pure hydrazines for pharmaceutical R&D

    2. Agrochemical Intermediate Manufacture

    Chemical formulators in the crop protection sector deploy this compound as a critical intermediate in the synthesis of hydrazone-based herbicides and fungicides. It is chosen for its reactivity with select aldehydes and ketones, producing high-yield intermediates applied in downstream formulation. Operators emphasize robust documentation for registrations in key agrochemical markets.

    Industry compliance standards

    • REACH registration for manufactured/imported quantities over 1 ton/year (EU)
    • ISO 9001:2015 quality management for production traceability
    • FAO and WHO pesticide specification references
    • China GB 2763 for agricultural chemical residue limits

    Typical usage ratio

    • 1.0–1.5 molar equivalents relative to aldehyde substrate
    • Adjusted based on intended hydrazone product activity and purification strategy

    Downstream process integration

    • Dosed during condensation reactions with crop-protection relevant substrates
    • Upstream from crystallization, solvent exchange, and extrusion into technical concentrates

    Final product types

    • Hydrazone herbicide technical intermediates
    • Systemic fungicide building blocks
    • Pre-formulation ingredients for downstream agrochemical products

    3. Specialty Polymer Chain-Terminator

    This chiral hydrazinecarboxaldehyde derivative functions as a specialty chain-terminator or cross-linker within high-performance polymer manufacturing. Downstream processors apply the compound during polycondensation stages for engineered plastics where precise molecular weight control and functional end-groups are required for advanced material properties.

    Industry compliance standards

    • ISO 9001:2015 for batch record and process control
    • RoHS 2011/65/EU (for polymers in restricted electronic applications)
    • EN 71-3 (applicability for polymers in consumer goods)
    • Global Automotive Declarable Substance List (GADSL), as relevant

    Typical usage ratio

    • 0.2–0.9 wt% in the total polymerization feed
    • Determined by desired polymer molecular weight, cross-link density, and application-specific requirements

    Downstream process integration

    • Introduced at final stage of monomer addition for precise end-capping
    • Reactive dosing controlled via in-line monitoring systems

    Final product types

    • Functional block copolymers for advanced coatings
    • High-performance plastics for electronics encapsulation
    • Cross-linked elastomers with novel thermal properties

    4. Advanced Organic Synthesis and Research Chemicals

    Contract manufacturing organizations (CMOs) and research labs integrate this compound as a protected hydrazine synthon for custom synthesis of complex heterocyclic compounds, ligands, and chiral catalysts. Its use in small- and pilot-scale operations requires documented chain-of-custody and advanced analytical support to ensure suitability for regulatory filings and scale-up.

    Industry compliance standards

    • ISO 17025-accredited analytical verification
    • Sigma-Aldrich TraceCERT supplying and documentation for R&D use
    • OECD GLP (for advanced research chemical processes)
    • REACH Annex XVII, as applicable for specialty lab chemicals in the EU

    Typical usage ratio

    • 0.9–1.1 molar equivalents in stepwise batch reactions
    • Optimized per project protocol and desired yield/purity profile

    Downstream process integration

    • Supplied as resin-stabilized solid or anhydrous solution
    • Applied in multistep organic synthesis for target molecule construction

    Final product types

    • Chiral ligands for asymmetric catalysis
    • Protected hydrazine intermediates for contract research
    • Novel heterocyclic compound scaffolds for medicinal chemistry
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    Certification & Compliance
    More Introduction

    2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde: Blending Innovation and Reliability in Chemical Synthesis

    Shaping the Future of Advanced Intermediates

    Launching a new intermediate into the fine chemical market never feels routine, especially with a molecule like 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde. This compound has roots in our development lines for chiral intermediates supporting pharmaceutical and research synthesis. Chemists searching for hand-in-glove selectivity find value in the stereochemistry embedded in this hydrazinecarboxaldehyde’s backbone. Every batch reflects years of quietly tuning process controls, watching chiral resolution in action, and chasing down unwanted isomerization—so an end-user can count on seeing the right configuration, not just close enough.

    Product Details Shaped by Real-World Feedback

    Through years of customer feedback and our own internal laboratory trials, we’ve landed on a model for this molecule that consistently delivers the (1S,2S) configuration, paired with a phenylmethoxy group at a key reactive position. Purity specification typically exceeds 98%, as confirmed through high-performance liquid chromatography and chiral column validation. Customers in specialty pharma and academic synthesis often report seamless phase transfer and consistent yield performance, particularly during hydrazone condensation steps. Fine details—like retention of the benzyl protection during downstream reactions—mean users can skip repeat purification or excessive process adjustment.

    Our plant team never just finishes a batch and sends it off. Each kilo of this hydrazinecarboxaldehyde gets monitored for residual solvents (always below 0.5%) and byproduct levels, including trace aldehyde or hydrazine starting materials. Internal systems trace every step from raw material testing to final packaging, using batch records maintained across several years, not merely for compliance but to guide process tweaks. Equipment cleaning and dedicated glass lines help fend off cross-contamination, especially for customers working under GMP guidance.

    Why This Molecule Means More Than a Catalog Item

    Chemically, the presence of the ethyl and phenylmethoxy groups drives application beyond basic hydrazine derivatives. In the field, project managers working on CNS-active compounds or new-generation pharmaceuticals tell us these substituents help adjust both reactivity and physicochemical properties. Certain hydrazone-forming processes struggle with less specialized analogs. Our customers—especially those running scale-ups in pilot plants—cite how the well-defined stereochemistry and purity sharpen both yield and isolation outcomes. When a hydrazone precursor brings in unwanted isomers or even minute degradation products, everything downstream feels the pain. In our plant, we run forced degradation studies monthly, cataloging impurities before they become anyone else’s problem.

    Designed for Performance: Small Detail, Big Impact

    The (1S,2S)-configured core changes more than just process chemistry. Working directly with synthetic groups at several multinational research sites, we see firsthand which impurities create headaches at bench or pilot scale. Our process avoids high-shear mixing near the end-point, favoring gentle stirring and temperature control, to preserve chiral integrity. Even at production scale, we use NMR and LC-MS cross-checks, so every output leaves with a solid data trail. The way the phenylmethoxy arm shields certain reactive centers often comes up in customer meetings. In reactions targeting heterocyclic frameworks, this substituent dampens side reactions and improves selectivity for the desired condensation, saving considerable labor in routine purifications.

    Feedback loops run both ways here. Internal QC reports flow directly back to our process chemistry labs. Technicians flag changes in melting points or solubility curves, which prompts quick root-cause hunting. On days when solvent purity slips at the raw material supplier, we’ve identified and stopped off-batch material even before it reached secondary packaging. This hands-on mindset means each drum lands in the user’s hands within spec, batch after batch.

    Clear Differences from Other Hydrazinecarboxaldehyde Intermediates

    This molecule earns its place with more than molecular weight and a chiral label. Traditional hydrazinecarboxaldehydes often lack strong stereocontrol, leading to multi-step troubleshooting in process lines. We learned early that minute drifts in chiral resolution lead to compounding process problems, so our synthetic route uses chiral catalysts sourced with validated provenance, and every incoming reagent gets identity confirmation. We do not blend or dilute product from multiple lots to “average” out purity—each batch tracks back to a single continuous run, ensuring reliable reproducibility.

    Pharmaceutical developers and synthetic chemists share a common frustration when a promising intermediate from a third-party arrives with uncertain configuration or mixed isomers. Our direct manufacturing pedigree matters. By controlling the synthesis environment and watching every step, we built a reliability layer both for regulatory documentation and for labs running high-value or tightly-timed projects. This single-source approach reduces variability, especially in compliant fields where each gram counts.

    Out in the field, researchers tell us they switched from lower-cost but non-stereospecific alternatives not just for improved yield but for fewer analytical surprises downstream. For customers matching analytical and process data across continents, batch-to-batch consistency makes a difference. Less time spent chasing analytical ghosts means research timelines stay on track.

    Applications Across Critical Fields

    Chiral hydrazinecarboxaldehyde intermediates play a pivotal role in active pharmaceutical ingredient development, especially as precursors for CNS agents, anti-cancer candidates, and various antifungals. Many of these molecules start with screening at the preclinical level, where small differences in impurity levels affect the biological profile. In our own R&D partnerships, major advances in chiral catalysis have translated into higher selectivity and yield for end-users. One partner doubled their hit rate in heterocycle libraries after moving to our tighter isomeric controls.

    Beyond pharma, academic groups lean on this intermediate for mechanistic studies in organic synthesis. We’ve seen practical use in asymmetric synthesis as a chiral auxiliary or template, giving chemists a new tool for building out libraries with sharper selectivity. The molecule’s robustness under a variety of reaction conditions—acidic, basic, or catalytically active—comes back in customer feedback cycles, where real-world stress-testing trumps lab-bench speculation.

    Addressing Real-World Challenges: Stability, Purity, and Supply

    Concerns about aldehyde stability surface regularly in discussions with process chemists. Our material ships with a validated shelf-life and careful moisture protection, down to the smallest laboratory pack. During pack-off, our team checks for water ingress, as hydrazone formation can proceed prematurely in the presence of even minor humidity. The packaging solution uses nitrogen blankets and low-permeability liners, extending stability well beyond a typical lab supply. These changes aren’t theoretical; they grew out of direct complaints from early adopters challenged by partial degradation at crucial steps.

    On the purity front, we address not only chemical content but also particulate contamination and solvent residues. QC analysts sample every lot post-filtration and review the data in real time, flagging out-of-trend results for immediate investigation. If heavier byproducts or unreacted hydrazine tails show up above actionable levels, our teams halt release and begin troubleshooting, not just for regulatory reasons, but to maintain trust with research programs that cannot afford uncertainty.

    Sourcing issues can often disrupt even the best-planned projects. We maintain forward stock of key raw materials from more than one qualified source, and each month brings a replanning cycle based on order flow and supplier reliability ratings. On more than one occasion, a supply chain disruption at a global scale sent demand our way. We pivot supply chain resources quickly, prioritizing core intermediates to keep our customers on schedule. Instead of third-party warehousing, our facilities manage stock directly, without sending product through layers of distribution that add risk and slowdowns.

    Long-Term Partnerships Built on Quality and Transparency

    One repeating theme with our research and scale-up customers centers on open access to documentation. Every shipment includes certificates detailing chiral purity, residual solvents, and full-elemental profiles. Customers stepping into regulatory submission stages benefit from ready-to-use supporting documentation. This level of transparency speeds up tech transfer, especially for multinational partners who must validate suppliers across several continents. For custom projects, our R&D group can provide split-lot samples, run custom specifications, or even adjust the protection strategy, aiding early-stage research where flexibility counts most.

    Some customers move beyond catalog orders, requesting off-books technical support. Application scientists from our team join regular calls with their process chemists, visiting plant sites to solve hands-on issues around scale-up, isolation, or final product stability. These conversations often circle back and drive new investment in our own labs, closing the loop between user feedback and product advancement.

    Environmental and Compliance Considerations at Core

    Regulatory shifts toward greener and more sustainable practices motivate our team to scrutinize every aspect of our process, from raw material selection to waste management. Where possible, we choose reaction conditions that minimize solvent use and lower waste output. Our waste management team routinely audits effluent treatment setups to ensure compliance and maintain local support for our production footprint.

    Trace levels of hazardous impurities cannot be pushed aside. Our analytical staff monitor for regulated compounds in both intermediate streams and the final product, readying full documentation packages for users in regulated fields. By addressing problem areas before customer audits reveal gaps, we’ve built a reputation as a supplier willing to engage detail at every scale.

    Beyond Manufacturing: Supporting Discovery and Development

    We see our role go beyond simply shipping drums. For customers confronting program stoppages owing to delayed intermediates or failed syntheses, a phone call to our technical desk can bring practical solutions—direct shipping, split lots, or in-process analytical support. Our development chemists frequently lend a hand in troubleshooting unexpected outcomes or suggesting alternate pathways using this hydrazinecarboxaldehyde as a starting point.

    Open-door policies with our largest buyers lead to early access to experimental batches, supporting pilot plant runs and first-in-human campaigns. Our plant’s flexibility means we can produce specialty grades or tailor outputs in response to unexplored synthetic challenges. These co-developed solutions often become standard offerings, closing process gaps and shortening the route from bench to bulk.

    Looking Ahead: Continuous Improvement in Specialty Chemical Supply

    Product launches are rarely just milestones for us—they mark new cycles of learning, constant listening, and slow, steady improvement in both process and product reliability. Each time we review customer trial reports, process maps, or deviation investigations, the lessons feed into process tweaks or equipment upgrades. Rather than focusing only on annual volume growth, we care just as much about minimizing deviations, boosting first-pass quality rates, and building trust one run at a time.

    The market doesn’t stand still. Regulatory guidance tightens, synthesis approaches shift, and applications multiply. We keep an eye on adaptation—scouting new chiral catalysts, optimizing protection group strategies, or refining packaging when stability signals warrant. Collaborative projects with academic and industrial R&D teams keep pushing both our standards and the molecule’s potential. This guidance from the field shapes everything from raw material screening to analytical method validation, securing the product’s value and relevance for the next wave of chemical innovation.

    Summary: Delivering Value by Embracing Detail

    Years of hands-on experience—tracking process variables, running pilot batches, answering urgent technical calls—have shaped how we deliver 2-[(1S,2S)-1-Ethyl-2-(Phenylmethoxy)Propyl]Hydrazinecarboxaldehyde. This isn’t just chemical manufacturing; it’s a trust-driven partnership with every chemist, project manager, and technical team counting on reliable, specific performance. The compound’s advanced profile, managed by processes rooted in real-world insight and open feedback channels, enables customers to move more quickly and confidently from bench to bulk. We’ll keep putting transparency, hands-on support, and relentless process improvement at the center of every shipment—because the needs of discovery-led teams demand nothing less.