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HS Code |
273211 |
| Iupac Name | 5-(4-Fluorophenyl)-1H-pyrazol-3-amine |
| Molecular Formula | C9H8FN3 |
| Molecular Weight | 177.18 g/mol |
| Cas Number | 864025-11-2 |
| Appearance | Solid (typically off-white to pale yellow powder) |
| Melting Point | 140-144 °C |
| Solubility | Soluble in DMSO, slightly soluble in methanol, ethanol |
| Smiles | C1=CC(=CC=C1C2=CC(=NN2)N)F |
| Inchi | InChI=1S/C9H8FN3/c10-7-3-1-6(2-4-7)8-5-9(11)13-12-8/h1-5H,11H2,(H,12,13) |
| Storage Conditions | Store at 2-8 °C, keep container tightly closed |
| Purity | Typically ≥98% |
| Synonyms | 4-Fluoro-5-(phenyl)-1H-pyrazol-3-amine |
As an accredited 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Opaque amber glass bottle containing 25 grams of 5-(4-Fluorophenyl)-2H-pyrazol-3-ylamine, labeled with hazard warnings and product details. |
| Shipping | 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine is shipped in tightly sealed containers, protected from moisture and light, and labeled according to chemical safety regulations. It is transported in compliance with local and international hazardous materials guidelines to ensure safe delivery, with all necessary documentation and safety data sheets included in the shipment. |
| Storage | Store **5-(4-Fluorophenyl)-2H-pyrazol-3-ylamine** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and restrict access to authorized personnel. Use personal protective equipment (PPE) when handling to avoid inhalation, ingestion, or direct skin contact. |
Applications of 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine in Industrial ManufacturingAs an established manufacturer of advanced pyrazole derivatives, we supply 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine for specialized applications across the agrochemical, pharmaceutical, dyes, and specialty chemical industries. Each segment below details exact usage contexts, covering regulatory standards, formulation requirements, process integration steps, and the definitive end-uses where this intermediate plays a critical role. 1. Agrochemical Active Ingredient Synthesis (Herbicides & Fungicides)Our material is a key intermediate in the synthesis of certain next-generation crop protection actives. Downstream producers use its pyrazole core to introduce selective weed and fungal resistance properties, especially relevant in high-value fruit and grain production. Its structure allows for targeted functionalization, compatibly integrating with other moieties to build novel agrochemical scaffolds where controlled bioactivity and low mammalian toxicity are essential. Industry compliance standards
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2. Pharmaceutical API Intermediate (Antiinflammatory & CNS Compounds)This compound serves as an advanced building block in the pharmaceutical sector, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and emerging central nervous system (CNS) therapeutics that target pyrazole receptors. Its fluorinated aromatic ring supports molecular stability and bioavailability profiles needed for regulatory approval in regulated drug synthesis. Industry compliance standards
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3. High-Performance Dye Intermediate (Organic Pigments)Major pigment and dye manufacturers use this compound to achieve highly stable color tones and resistance to photobleaching in specialty textile and plastic masterbatches. The fluorinated pyrazole scaffold supports the synthesis of advanced diazo and azo dyes used in the demanding automotive, fashion, and packaging sectors, where colorfastness is non-negotiable. Industry compliance standards
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4. Specialty Chemical Building Block (Heterocycle Synthesis & Electronic Materials)Our pyrazole compound is also deployed in specialty chemical operations, particularly in the construction of advanced heterocyclic scaffolds for electronic materials, sensors, or performance coatings. The fluorine substituent confers unique electron-withdrawing properties, valuable in tuning charge transport and thermal stability for downstream polymer or liquid crystal applications. Industry compliance standards
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