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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 | 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. |
Applications of 1-(3-Chlorophenyl)-3-Methyl-4,5-Dihydro-1H-Pyrazol-5-One in Industrial ManufacturingAs 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 AnalgesicsThis 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
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2. Agrochemical Intermediate for Selective Herbicide ProductionOur 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
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3. Colorant and Dye Intermediate: Specialty Pyrazolone PigmentsManufacturers 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
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4. Research Intermediate for Novel Pyrazolone Scaffold LibrariesLeading 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
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