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(4-Benzyl-1,4-Oxazinan-2-Yl)Methanol

    • Product Name (4-Benzyl-1,4-Oxazinan-2-Yl)Methanol
    • Alias (4-benzylmorpholin-2-yl)methanol
    • Einecs 639-626-8
    • 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

    385379

    Chemical Name (4-Benzyl-1,4-oxazinan-2-yl)methanol
    Molecular Formula C11H15NO2
    Molecular Weight 193.24 g/mol
    Cas Number 1423794-53-1
    Appearance White to off-white solid
    Purity Typically ≥ 98%
    Solubility Soluble in polar organic solvents
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles OCc1cn(CC2=CC=CC=C2)co1
    Inchi InChI=1S/C11H15NO2/c13-8-11-12-7-10(6-9-14-11)15-5-3-1-2-4-5/h1-2,5-6,10,13H,3-4,7-9H2
    Synonyms 2-(Hydroxymethyl)-4-benzyl-1,4-oxazinan

    As an accredited (4-Benzyl-1,4-Oxazinan-2-Yl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25g amber glass bottle with a secure screw cap, clearly labeled with compound name and safety information.
    Shipping (4-Benzyl-1,4-oxazinan-2-yl)methanol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported under ambient conditions unless otherwise specified, with careful labeling and documentation in compliance with hazardous material regulations. Appropriate safety precautions are followed during handling, including the use of protective equipment if necessary.
    Storage Store (4-Benzyl-1,4-oxazinan-2-yl)methanol in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizing agents. Keep the storage area cool, dry, and well-ventilated, preferably at room temperature. Label the container clearly and store it in a designated chemical cabinet to prevent contamination or accidental misuse. Ensure proper chemical handling protocols are followed.
    Application of (4-Benzyl-1,4-Oxazinan-2-Yl)Methanol

    Applications of (4-Benzyl-1,4-Oxazinan-2-Yl)Methanol in Industrial Manufacturing

    As an established chemical raw material manufacturer, we have developed and refined the industrial-scale production of (4-Benzyl-1,4-Oxazinan-2-Yl)methanol to serve targeted sectors where its structure and functional properties match clearly defined market demands. This substance is widely utilized as a high-purity building block for complex synthesis, finding substantial use in pharmaceutical intermediates, fine chemical synthesis, agricultural chemical R&D, and advanced polymer modification. The following application areas represent genuinely adopted and validated scenarios by global industry, each with distinct requirements for integration, regulatory compliance, formulation optimization, and end-product outcomes.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical companies source this compound as a core intermediate for the manufacture of selective serotonin receptor modulators and CNS-targeted therapeutic precursors. Our facility supplies GMP-grade material that integrates directly into multi-step API synthesis where precise control over chiral purity and batch consistency are critical. Rigid batch traceability ensures compound uniformity essential for regulatory filings and downstream QC protocols, especially for patented synthetic routes in anxiety and depression drug development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • USP-NF Monographs (as applicable for intermediates)
    • 21 CFR Part 210/211 (US FDA cGMP for pharmaceuticals)

    Typical usage ratio

    • 5–15% of molar ratio relative to the target heterocyclic scaffold; specific inclusion determined by stepwise equivalence in API synthesis and route optimization

    Downstream process integration

    • Incorporated at the intermediate coupling stage via reductive amination or substitution reaction; used directly after purification and solvent switch procedures; integrated in both batch and continuous flow reactors

    Final product types

    • Active pharmaceutical ingredients (APIs) targeting CNS disorders
    • Research compounds for clinical trials
    • Characterized pharmaceutical intermediates (for downstream contract synthesis)

    2. Fine Chemical Synthesis for Specialty Building Blocks

    Specialty synthesis firms utilize this material as a cornerstone for custom heterocycle assembly and the creation of complex molecular fragments for catalogue libraries. Controlled reactivity enables precise functional group transformations essential for lead candidate development and SAR studies in medicinal chemistry. Consistent supply of this compound supports pilot and full-scale commercialization under rigorous documentation and batch homogeneity standards relevant to ISO-certified fine chemical operations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Responsible Care® initiatives for chemical manufacturing
    • REACH Registration (EC No. 1907/2006, as manufactured/imported in EU)

    Typical usage ratio

    • 2–8% w/w or as dictated by stoichiometric requirements for fragment coupling and heterocyclic assembly; adjusted based on the desired substitution degree during batch/continuous operation

    Downstream process integration

    • Added during controlled-temperature condensation or N-alkylation reactions; post-reaction deprotection and crystallization steps ensure isolation of high-purity intermediates for final synthetic transformations

    Final product types

    • Pharmaceutical research intermediates
    • Agrochemical scaffolds for structure-activity analysis
    • Heterocyclic reference standards for analytical laboratories

    3. Advanced Polymer Functionalization

    Manufacturers of high-performance polymers rely on this compound as a reactive modifier, introducing nitrogenous moieties into specialty polymers for enhanced adhesion, biocompatibility, or mechanical resilience. Melt-phase and solution-phase integrations target high-end applications, including specialty coatings and biomedical device encapsulants, with strict batch-to-batch reactivity and migration profile controls aligning with processing ISO norms.

    Industry compliance standards

    • ISO 10993-1: Biological evaluation of medical devices (when used for biocompatible polymers)
    • ISO 9001 Quality Management System
    • RoHS Directive 2011/65/EU for electronic coatings

    Typical usage ratio

    • 0.1–2.5% by weight for masterbatch blending; fine-tuned according to target cross-link density and performance endpoints specified in technical data sheets

    Downstream process integration

    • Blended into polymer melt using twin-screw extrusion or introduced during pre-polymerization steps in solution processes; post-functionalization monitored by FTIR and tensile testing

    Final product types

    • Biomedical-grade polymer encapsulants
    • High-adhesion specialty coatings for electronics
    • Modified thermoplastics for engineering applications

    4. Crop Protection Agent R&D and Analytical Reference

    Innovative agrochemical research groups and analytical service providers utilize this compound for elucidating structure-activity relationships in new crop protection molecules. Used as a reference standard or as a reactive intermediate in the development of fungicidal actives, product quality and trace-level impurity control are managed by state-of-the-art analytical protocols, supporting regulatory submissions and field trial formulations.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • ISO/IEC 17025 Accreditation for chemical testing laboratories
    • FAO/WHO Specifications for pesticide testing (where applicable for reference)

    Typical usage ratio

    • Utilized as a trace-level analytical reference; as a synthetic building block, the addition typically ranges from 1–10% of the molar ratio to the core scaffold, determined by quantum yield and reactivity of the candidate active

    Downstream process integration

    • Integrated during the lead optimization step in chemical R&D workflows; used for derivatization in synthetic sequence trials and as a standard in GC-MS or HPLC characterization protocols

    Final product types

    • Novel fungicidal or pesticidal actives for field testing
    • Reference standards for accredited analytical laboratories
    • Advanced intermediates for internal pipeline screening
    Free Quote

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