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3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid

    • Product Name 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid
    • Alias CMICA
    • Einecs 630-463-6
    • 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

    408965

    Chemical Name 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid
    Molecular Formula C11H8ClNO3
    Molecular Weight 237.64 g/mol
    Cas Number 130400-57-4
    Appearance White to off-white solid
    Melting Point Approx. 170-174 °C
    Solubility Slightly soluble in water, soluble in DMSO and ethanol
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light
    Smiles CC1=CC(=NO1)C2=CC=CC=C2ClC(=O)O
    Iupac Name 3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid

    As an accredited 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle, labeled "3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid", sealed, with hazard warnings.
    Shipping The chemical *3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid* is shipped in sealed, high-density polyethylene containers to prevent moisture and contamination. Packages are labeled according to regulatory requirements, with safety data sheets included. Temperature control and hazard classification are considered to ensure safe, compliant transport during domestic or international shipping.
    Storage Store **3-(2-Chlorophenyl)-5-methylisoxazole-4-carboxylic acid** in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C) in a well-ventilated, dry area away from incompatible substances such as strong acids, bases, and oxidizers. Ensure proper chemical labeling and secure storage to prevent unauthorized access or accidental release.
    Application of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid

    Applications of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid in Industrial Manufacturing

    As a dedicated manufacturer of specialty intermediates, we supply 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid to global chemical producers for incorporation into advanced downstream synthesis. Below, we detail specific industrial application scenarios with their unique requirements, processing methods, and end-use products, reflecting our insight into practical B2B use cases for this material.

    1. Pharmaceutical Intermediate for Isoxazole-Based APIs

    Drug manufacturers utilize this compound primarily as a critical step in the synthesis of several isoxazole ring-containing active pharmaceutical ingredients, especially within the anti-inflammatory and CNS therapeutic segments. Its structure allows precise functionalization, supporting the formation of complex molecules through controlled reactions during multi-stage synthesis lines under strict quality assurance systems.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • European Pharmacopoeia monographs (Ph. Eur.) relevant to starting materials
    • United States Pharmacopoeia (USP) general chapters for API synthesis
    • China Pharmacopoeia raw material guidelines

    Typical usage ratio

    • Usage typically ranges from 12% to 23% w/w of reaction mixture depending on the target API and yield optimisation, and is determined by molar equivalence required in the condensation or cyclization stage.

    Downstream process integration

    • Introduced during the early to mid-stages of multi-step organic synthesis, serving as a key intermediate or coupling partner in batch hydrogenation, halogenation, or amidation steps under temperature- and solvent-controlled conditions.

    Final product types

    • Isoxazole-based anti-inflammatory drug APIs
    • CNS-active pharmaceutical compounds
    • Analogue building blocks for patent and generic molecules
    • Fine chemical standards for pharmaceutical R&D

    2. Agrochemical Intermediate for Isoxazole Herbicides and Fungicides

    Formulators in agrochemical manufacturing employ this raw material as an isoxazole ring donor in synthesizing selective herbicide and fungicide actives. The chlorophenyl substitution provides enhanced target specificity and environmental stability, resulting in improved field persistence for end-use formulations targeting weed and fungal resistance in major crops.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • EPA TSCA (Toxic Substances Control Act) registration for intermediates
    • REACH (EC 1907/2006) compliance for imported intermediates
    • ISO 9001:2015 system for batch traceability

    Typical usage ratio

    • Dosing commonly falls in the 8% to 16% w/w range, based on the desired loading of the isoxazole moiety in the final pesticide molecule, often determined by target LC50 requirements and synthetic efficiency.

    Downstream process integration

    • Added directly into the core synthesis step for active ingredient generation, typically through nucleophilic substitution or cyclization sequences under anhydrous and inert conditions, with direct integration into agrochemical API isolation lines.

    Final product types

    • Pre-emergent and post-emergent herbicide AI powders
    • Systemic fungicide concentrate APIs
    • Agrochemical technical concentrates shipped to formulation plants
    • R&D samples for crop-protection screening

    3. Fine Chemical Synthesis Building Block for Specialty Dyes and Pigments

    Specialty chemical producers use this carboxylic acid derivative as a building block for synthesizing advanced isoxazole chromophores, enabling the development of high-performance dyes and pigments with unique spectral and stability characteristics for plastic coloration, ink, and coating sectors. Its structural attributes allow precision in functional group introduction, facilitating the creation of tailor-made colorants with thermal and lightfast properties.

    Industry compliance standards

    • EN 71-3 Safety of Toys – Migration of Certain Elements (for colorant use)
    • REACH Regulation (Annex XVII for dye intermediates)
    • ISO 9001:2015 quality management for pigment synthesis
    • ASTM D01 standards for organic coloring materials

    Typical usage ratio

    • Concentration usually varies from 3% to 9% w/w in reaction feeds, adjusted according to the targeted shade depth, chroma and required reactivity for subsequent coupling or condensation steps.

    Downstream process integration

    • Charged during the heterocycle assembly or as an acylating agent in pigment and dye synthesis reactors, often alongside auxiliary amines or phenols, prior to the final purification and isolation of solid colorant intermediates.

    Final product types

    • Solvent-resistant organic pigments
    • Specialty dyes for technical textiles
    • UV-stable inks for security marking
    • Melt-stable colorants for plastics compounding

    4. Chemical Reagent for Isoxazole Scaffold Research and Analytical Reference Materials

    Research laboratories and analytical standards producers procure this isoxazole derivative for use as a reference material or scaffold in the synthesis of structurally related molecules, particularly during the development of new bioactive compounds and in method validation QC protocols. The compound’s high purity and defined substitution pattern facilitate accurate calibration and extended structure-activity relationship (SAR) studies.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • OECD Good Laboratory Practice (GLP)
    • USP Reference Materials acceptance criteria
    • ISO 19011 for laboratory audits

    Typical usage ratio

    • Applied typically at 0.05%–0.5% w/w in research synthesis runs or at concentrations of 50–200 mg/L in analytical standard preparations, selected based on detection sensitivity and analytical instrumentation limits.

    Downstream process integration

    • Dissolved or weighed-in during preparative synthesis, assay calibration, or verification of synthetic routes in compound library creation for structural and functional analysis pipelines.

    Final product types

    • Reference standards for analytical QC
    • Research-grade isoxazole analogues for structural studies
    • SAR screening libraries supplied to pharmaceutical discovery teams
    • Analytical calibration sets for chromatographic systems
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