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HS Code |
707328 |
| Chemical Name | Pivalamide |
| Iupac Name | 2,2-dimethylpropanamide |
| Molecular Formula | C5H11NO |
| Molar Mass | 101.15 g/mol |
| Cas Number | 563-68-8 |
| Appearance | White crystalline solid |
| Melting Point | 161-163 °C |
| Solubility In Water | Slightly soluble |
| Density | 0.926 g/cm³ |
As an accredited Pivalamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pivalamide is packaged in a 100g amber glass bottle with a secure, screw-cap lid, labeled with hazard and product information. |
| Shipping | Pivalamide is shipped in tightly sealed containers, protected from moisture and light. It should be handled with standard chemical safety precautions. The packaging complies with relevant regulations for non-hazardous chemicals, ensuring secure transport. Shipment is typically via ground or air, accompanied by a safety data sheet and appropriate labeling. |
| Storage | Pivalamide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep it away from sources of ignition and heat. Store at room temperature, and avoid exposure to moisture. Proper labeling and adherence to all safety and regulatory guidelines for chemical storage are recommended. |
Applications of Pivalamide in Industrial ManufacturingAs a direct manufacturer of pivalamide, we support a range of chemical industries by providing consistently high-purity material that meets stringent supply chain and quality demands. Below we outline major industrial application scenarios for pivalamide, structured by downstream sectors, use contexts, and regulatory compliance requirements, enabling efficient integration into your production processes. 1. Agrochemical Intermediate SynthesisPivalamide acts as a prominent building block in the synthesis of various herbicide and fungicide active ingredients, favored for its chemical stability and amide functional group compatibility during multi-step organic reactions. It is introduced during the synthesis of N-alkylated or N-acylated intermediates, tailored for selective mode-of-action agrochemicals, especially in high-value crop protection formulations. The precise dosage can affect both process efficiency and subsequent purification requirements. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingMany pharmaceutical active pharmaceutical ingredient (API) synthesis routes rely on pivalamide as both an amide coupling partner and a reagent for introducing sterically-hindered motifs. This material frequently appears in patented routes for beta-lactam antibiotics and specific antiretroviral precursors due to its well-defined impurity profile, facilitating GMP-compliant API and intermediate manufacturing flows. Industry compliance standards
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3. Specialty Polymer Modifier ProductionSynthesizers of performance polymers utilize pivalamide as a co-monomer or functional group donor to impart steric resistance, thermal stability, or improved solvent resistance in end-use engineering plastics and advanced resins. Its participation as a chain modifier requires controlled dosing to prevent unwanted cross-linking, supporting fine-tuning of final mechanical properties in downstream compounding and extrusion. Industry compliance standards
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4. Fine Chemical Synthesis (Hindered Amide Reactions)Chemical manufacturers engaged in fine chemical synthesis value pivalamide for its application in sterically demanding amidation reactions, including the preparation of specialty esters, hindered amines, and catalysts. The controlled introduction of bulky amide groups directly impacts reaction selectivity and reduces side-product formation in multi-functional molecule assembly lines, making process optimization essential for purity and cost efficiency. Industry compliance standards
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5. Photoinitiator and UV Stabilizer Component ManufacturingManufacturers of advanced photoinitiators and UV absorber systems employ pivalamide as a key intermediate for introducing sterically hindered amide moieties. This approach boosts photostability and migration resistance in products for industrial inks, adhesives, and high-performance coatings. Process control demands careful incorporation to maximize reactivity and shelf-life stability of the downstream light-activated compounds. Industry compliance standards
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Tel: +8615371019725
Email: admin@sinochem-nanjing.com
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