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1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One

    • Product Name 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One
    • Alias 3-Chloro-4-methylphenyl pyrazolone
    • Einecs 687-640-1
    • 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

    757322

    Iupac Name 1-(3-Chlorophenyl)-3-methyl-4,5-dihydro-1H-pyrazol-5-one
    Molecular Formula C10H9ClN2O
    Molecular Weight 208.65 g/mol
    Appearance White to off-white crystalline powder
    Melting Point Approximately 180-184°C
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Boiling Point Decomposes before boiling
    Density Approx. 1.32 g/cm³ (estimated)
    Structure Type Pyrazolone derivative
    Smiles CC1=NN(C2=CC(=CC=C2)Cl)C(=O)C1
    Synonyms 3-Methyl-1-(3-chlorophenyl)-4,5-dihydro-1H-pyrazol-5-one
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap. White label displays chemical name, quantity, CAS number, and hazard symbols.
    Shipping This chemical, 1-(3-Chlorophenyl)-3-methyl-4,5-dihydro-1H-pyrazol-5-one, should be shipped in a tightly sealed container, protected from light and moisture. It must be clearly labeled and packed according to relevant chemical transport regulations, with appropriate hazard labeling, and shipped by certified carriers with accompanying safety documentation (SDS).
    Storage Store **1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One** in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and avoid exposure to heat sources. Store under controlled room temperature and restrict access to authorized personnel only.
    Application of 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One

    Applications of 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One in Industrial Manufacturing

    As a core manufacturer of 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One, we support advanced industrial production through targeted supply of this specialty intermediate. Our direct engagement with downstream processors ensures proven functionality across key sectors. Below, we detail sector-specific applications, compliance, usage levels, and integration with downstream manufacturing.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Pyrazolone-Based Analgesics

    This raw material functions as a critical building block in the synthesis of certain pyrazolone-class analgesic intermediates. Process chemists utilize its chemical reactivity for condensation and cyclization reactions, forming core moieties required for non-opioid pain relief APIs. Reaction parameters and molar ratios are set based on final product specification. Our material’s purity supports robust in-process controls during pharmaceutical manufacturing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP 21 CFR Part 210/211)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for API intermediates
    • ICH Q3A/B guidelines on impurities
    • REACH (EC) No 1907/2006 registration for pharmaceutical use

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents relative to the subsequent aldehyde or amine, based on the target molecule
    • Specific ratio adjusted for target substitution pattern and impurity profile

    Downstream process integration

    • Charged to the initial condensation reactor during intermediate stage synthesis
    • Purified through crystallization and solvent extraction before downstream cyclization
    • Monitored by HPLC and GC analysis at each critical step

    Final product types

    • Metamizole sodium (NSAID precursor)
    • Antipyrine derivatives
    • Analgesic and antipyretic pharmaceutical APIs

    2. Agrochemical Intermediate for Selective Herbicide Production

    Our material serves as a strategic pyrazolone core for synthesis of herbicide intermediates, mainly in the development of selective post-emergent weed control products for cereal and maize cultivation. Formulators use its substituent pattern to direct desired biological activity. The molecule enters key steps of functional group introduction and isomer separation. Controlled addition ensures crop safety and application precision.

    Industry compliance standards

    • ISO 9001:2015 certified quality management throughout production
    • Regulation (EC) No 1107/2009—Plant Protection Products
    • FAO/WHO specifications for technical material and formulated herbicides
    • OECD Test Guidelines for environmental and toxicological data

    Typical usage ratio

    • Typically 1.05–1.15 molar equivalents per target chlorination or alkylation reaction
    • Adjusted based on batch size and conversion efficiency measured during process validation

    Downstream process integration

    • Undergoes initial activation or halogen exchange in intermediate synthesis
    • Passes through purification, usually involving silica gel chromatography
    • Incorporated prior to the final step of formulating high-purity herbicide actives

    Final product types

    • Selective post-emergent herbicides for wheat, corn, and rice
    • Custom herbicide intermediates for regional markets
    • Precursor chemicals for future agrochemical R&D pipelines

    3. Colorant and Dye Intermediate: Specialty Pyrazolone Pigments

    Manufacturers in the pigment sector utilize this pyrazolone derivative to synthesize arylazo-based pigments known for strong tinctorial strength and weather fastness. Fine chemical producers couple it with diazonium salts to create stable pigment lakes. Our material’s tracked impurity levels minimize unwanted byproducts and achieve batch-to-batch consistency for textile and coating applications.

    Industry compliance standards

    • EN 71-3:2019 for pigment safety in toys
    • ISO 787-24 for pigment identification and purity
    • REACH compliance regarding azo content and heavy metals
    • ZDHC MRSL 3.0 for sustainable textile chemistry

    Typical usage ratio

    • Standard coupler:diazonium ratio of 1:1 (mole:mole); may be screened at 0.9–1.1 ratio for color depth optimization
    • Blending with minor co-monomers permissible at less than 5% of reaction mass

    Downstream process integration

    • Participates in azo coupling process after pre-neutralization
    • Filtered and washed to remove inorganic salts and unreacted precursors
    • Subjected to milling and surface treatment prior to dispersion in end-use formulations

    Final product types

    • Yellow and orange pigments for printing inks
    • High weather-resistant colorants for plastics
    • Pigment preparations for textile dyeing

    4. Research Intermediate for Novel Pyrazolone Scaffold Libraries

    Leading CROs and medicinal chemistry firms require pyrazolone-based scaffolds for rapid library synthesis and SAR (structure-activity relationship) studies. Our intermediate fits demanding purity parameters for high-throughput combinatorial reactions. Researchers value its consistent reactivity for automated synthesis, hit-to-lead generation, and scaling up promising tool compounds for further development.

    Industry compliance standards

    • ISO 17034 for certified reference material preparation
    • OECD GLP (Good Laboratory Practice) for research batch supply
    • Analysis in compliance with ICH Q7
    • Registration with local chemical cataloging authorities as per 40 CFR Part 720 (TSCA Inventory, USA)

    Typical usage ratio

    • Introduction to library syntheses at 1:1 stoichiometry with various electrophiles or nucleophiles
    • Concentration flexibility: 0.1–0.5 mmol per reaction in microplate formats, or scale up as needed

    Downstream process integration

    • Delivered as pre-weighed solids or stock solutions for automated dispensing
    • Used in parallel synthesis with diverse linkers and functional groups
    • Analytical QC includes LC-MS, HPLC, and NMR validation for each generated compound

    Final product types

    • Target-validated small molecule libraries
    • Reference compounds for screening
    • Building blocks for fragment-based drug discovery
    Free Quote

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