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HS Code |
834441 |
| Chemical Name | 3-Methyl-3-pyrazolin-5-one |
| Molecular Formula | C4H6N2O |
| Molecular Weight | 98.10 g/mol |
| Cas Number | 5464-14-2 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 162-164°C |
| Solubility In Water | Moderately soluble |
| Density | 1.26 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Ph | Neutral to slightly basic in aqueous solution |
| Storage Temperature | Store at room temperature, tightly closed |
| Smiles | CC1=NNC(=O)C1 |
As an accredited 3-Methyl-3-Pyrazolin-5-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Methyl-3-Pyrazolin-5-One, sealed with a screw cap and labeled with hazard symbols. |
| Shipping | 3-Methyl-3-pyrazolin-5-one is shipped in tightly sealed containers, protected from light and moisture, and clearly labeled according to chemical transport regulations. It is handled as a stable, non-flammable solid, but should be kept away from incompatible substances. Transport follows relevant safety guidelines, ensuring secure packaging to prevent leaks or contamination. |
| Storage | **3-Methyl-3-Pyrazolin-5-One** should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture, direct sunlight, and sources of ignition. Store at room temperature, and ensure proper labeling. Use appropriate safety measures, including secondary containment to prevent spills or accidental release. |
Applications of 3-Methyl-3-Pyrazolin-5-One in Industrial ManufacturingAs a specialized manufacturer, we supply 3-Methyl-3-Pyrazolin-5-One for downstream companies using this advanced heterocyclic compound in high-value industrial production. This page details the real-world application scenarios based on established formulations, industry standards, and documented manufacturing practices in key sectors. 1. Pharmaceutical Intermediate for Antipyretic and Analgesic APIsMajor pharmaceutical firms employ 3-Methyl-3-Pyrazolin-5-One as an essential intermediate during production of antipyrine-based APIs, such as metamizole sodium (analgin). This raw material contributes a stabilized pyrazolone structure during multi-step organic synthesis, providing a safety and efficacy profile acceptable to international medicine regulatory bodies. Proper handling and batch monitoring ensure purity and traceability in every lot processed under regulated GMP conditions from the synthesis through the API stage. Industry compliance standards
Typical usage ratio
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2. Synthesis of Dye Intermediates for Azo and Reactive DyesDye manufacturers incorporate 3-Methyl-3-Pyrazolin-5-One as a key nucleophilic heterocycle to enable synthesis of specific dye intermediates, especially for advanced azo and reactive dye lines. The compound’s unique ring structure participates in diazotization and coupling reactions, directly impacting colorfastness and chromatic intensity in the final pigment dispersions. Strict controls during synthesis guarantee standardized color parameters required in international textile and pigment markets. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Chemical Stabilizer in Photographic Chemical FormulationsTraditional and specialty photographic chemical manufacturers utilize 3-Methyl-3-Pyrazolin-5-One as a stabilizer and scavenger in color developer solutions. Its molecular configuration helps inhibit unwanted side reactions and oxidative degradation during film processing, supporting the preservation of image clarity and shelf life for professional imaging chemicals. Integration at controlled rates and concentrations occurs under cleanroom conditions to meet the needs of digital and silver-halide system users. Industry compliance standards
Typical usage ratio
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4. Intermediate for Agrochemical Heterocycle SynthesisAgrochemical producers apply 3-Methyl-3-Pyrazolin-5-One during multi-stage synthesis of select crop protection agents, especially those based on pyrazolone and triazolone chemistries. It functions as a privileged building block for scaffolding new actives possessing both insecticidal and herbicidal modes of action. Tight controls over charge-in, reaction temperature, and sequential purification ensure compliance with regulatory impurity thresholds recognized by global agrochemical authorities. Industry compliance standards
Typical usage ratio
Downstream process integration
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Email: admin@sinochem-nanjing.com
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