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Benzo[D]Isoxazol-3-ol

    • Product Name Benzo[D]Isoxazol-3-ol
    • Alias 3-Hydroxybenzo[d]isoxazole
    • Einecs 629-334-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    337399

    Iupac Name 1,2-benzoxazol-3-ol
    Molecular Formula C7H5NO2
    Molecular Weight 135.12 g/mol
    Cas Number 32743-06-3
    Appearance Off-white to beige solid
    Melting Point 180-183°C
    Solubility In Water Slightly soluble
    Smiles Oc1c[nH]c2ccccc12
    Inchi InChI=1S/C7H5NO2/c9-6-5-8-7-4-2-1-3-6/h1-5,9H
    Pubchem Cid 14318305
    Synonyms Benzo[d]isoxazol-3-ol; 3-Hydroxybenzo[d]isoxazole

    As an accredited Benzo[D]Isoxazol-3-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Benzo[D]Isoxazol-3-ol, 25g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled with hazard and safety information.
    Shipping Benzo[D]Isoxazol-3-ol is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Packaging complies with chemical safety regulations to prevent leaks or contamination. Appropriate hazard labeling and documentation are included. Shipments commonly require ground or air transport with careful handling as a laboratory chemical.
    Storage Benzo[D]Isoxazol-3-ol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Store at room temperature or as specified by the manufacturer. Follow proper laboratory safety protocols when handling and storing this chemical.
    Application of Benzo[D]Isoxazol-3-ol

    Applications of Benzo[D]Isoxazol-3-ol in Industrial Manufacturing

    Benzo[D]Isoxazol-3-ol serves as a critical intermediate in several highly controlled chemical synthesis routes. Our manufacturing partners apply this raw material in various industrial contexts where consistent quality and strict adherence to regulatory standards are required. Below are key downstream application scenarios in which this compound plays a dedicated and specialized role.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antipsychotic Drugs

    Pharmaceutical companies use this compound extensively as a core building block in the synthesis of certain antipsychotic APIs, with risperidone manufacturing being the leading example. The process demands high-purity raw materials to comply with international pharmacopoeia and GMP systems. Integrators introduce the compound during the initial condensation and cyclization stages, where it acts as a precursor unit. Precise control of stoichiometry ensures consistent yield and eliminates formation of undesired isomeric by-products. The end product supplies finished drug manufacturers for global distribution.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) Monographs
    • United States Pharmacopeia (USP) requirements for APIs
    • Good Manufacturing Practice (ICH Q7, EU GMP Part II)
    • Japanese Pharmacopoeia (JP)

    Typical usage ratio

    • 1.0 to 1.1 molar equivalent, dependent on target antipsychotic API synthesis batch size
    • Adjustment based on impurity profile and targeted purity for final API

    Downstream process integration

    • Included in initial heterocyclic condensation phase
    • Feeds cyclization and subsequent functionalization stages of drug intermediate synthesis
    • Subjected to purification before coupling with secondary amines or other pharmacophoric groups

    Final product types

    • Commercially formulated antipsychotic tablets (e.g., risperidone)
    • Injectable depot formulations of atypical antipsychotics
    • Finished pharmaceutical bulk substances supplied to licensed generic API producers

    2. Agrochemical Intermediate for Custom Pesticide Synthesis

    Agrochemical manufacturers employ this compound for the production of selective herbicide intermediates. Its isoxazole structure supports specific crop protection chemistries, where it reacts with alkylating agents during the synthesis of pre-emergent weed killers. Downstream processors require strict conformance to agricultural chemical standards, including extensive traceability and zero-relevant impurity thresholds. The synthesis bench determines the optimal dosing based on target yield and desired activity spectrum.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) pesticide specifications
    • ISO 9001:2015 Quality Management System
    • REACH registration and CLP (Classification, Labelling and Packaging) Regulation
    • OECD Guidelines for Testing of Chemicals (GLP-compliant synthesis)

    Typical usage ratio

    • 0.8–1.2 molar equivalent in precursor synthesis, fine-tuned according to end herbicide formulation
    • Adjustable for impurity control, with analytical verification

    Downstream process integration

    • Introduced at condensation or alkylation stages to build bioactive isoxazole derivatives
    • Subjected to hydrolysis or further functionalization as needed for target agent
    • Yield monitored through HPLC tracking of intermediate conversion

    Final product types

    • Concentrated herbicide active substances for post-blending
    • Pre-packed herbicidal suspension concentrates (SCs) and wettable granules (WGs)
    • Custom crop protection compounds for OEM agrochemical brands

    3. Specialty Chemical Intermediate for Dye and Pigment Manufacturing

    Dye producers value the compound as a specialized intermediate in high-performance pigment synthesis, particularly for heat-resistant organic dyes. It structures pigment molecules with increased stability and lightfastness. Manufacturers typically add the compound during complex azo-coupling or ring-closure sequences. Precise batch calibration ensures color purity and performance. Downstream partners monitor compliance with environmental and workplace exposure regulations to meet market and customer safety expectations.

    Industry compliance standards

    • EN 71-3 (Toy Safety - migration of certain elements)
    • Oeko-Tex Standard 100 (Textile chemical safety)
    • REACH Annex XVII (Restrictions on certain dangerous substances)
    • Global harmonization per GHS SDS (Globally Harmonized System)

    Typical usage ratio

    • 3–10% w/w based on total pigment synthesis mass
    • Varies according to target chromophore and desired dye depth

    Downstream process integration

    • Participates in nucleophilic aromatic substitution or coupling reactions
    • Introduced during colorant backbone construction for stability enhancement
    • Subjected to post-synthesis refining and finishing steps

    Final product types

    • High-performance textile dyes and colorants
    • Organic pigments for plastics and coatings
    • Specialty inkjet and screen printing dyes for industrial use

    4. Research and Development Reagent for Custom Organic Synthesis

    Contract research organizations (CROs) and in-house R&D teams commonly order this chemical for new chemical entity (NCE) development, heterocycle construction, and pathway optimization studies. Usage is strictly monitored, and the process often involves stepwise reactions to explore new molecular frameworks or analogues. Labs consult up-to-date chemical safety legislation and work under certified management systems, with formulation parameters changing based on individual project objectives. The resulting materials become part of larger project milestones or preclinical sample batches.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO/IEC 17025 (General requirements for competence of testing and calibration laboratories)
    • REACH pre-registration and notification (for research-scale activities)
    • Local chemical safety regulations (country specific)

    Typical usage ratio

    • 0.1–2.0 molar equivalent, dependent on synthetic route under study
    • Totally project-specific, adjusted per reaction step and target scaffold

    Downstream process integration

    • Used during lead compound generation or scaffold innovation in the first reaction step
    • May enter as a nucleophile or electrophile, depending on pathway
    • Purification via chromatography or crystallization follows each stage

    Final product types

    • Intermediate NCE libraries and reference standards
    • Lead candidate molecules for preclinical screening
    • Analytical standards for validation of emerging drug or agrochemical candidates
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