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Pivalamide

    • Product Name Pivalamide
    • Alias N-Pivalamide
    • Einecs 208-845-3
    • 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

    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 & Storage
    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.
    Application of Pivalamide

    Applications of Pivalamide in Industrial Manufacturing

    As 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 Synthesis

    Pivalamide 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

    • Regulation (EC) No 1107/2009 for plant protection products
    • REACH Regulation (EC) No 1907/2006
    • FAO/WHO International Code of Conduct on Pesticide Management
    • ISO 9001:2015 for quality management systems in chemical manufacturing

    Typical usage ratio

    • 1.5–6% by weight of total reaction mass, adjusted according to desired alkylation/acylation level and downstream reagent loading

    Downstream process integration

    • Added during the amide bond-forming step or utilized as a protective group precursor in active substance synthesis; undergoes controlled reaction followed by stepwise downstream separation and formulation purification.

    Final product types

    • Herbicide technical concentrates (e.g., ALS inhibitors, substituted amide actives)
    • Fungicide APIs for broad-spectrum seed coatings

    2. Pharmaceutical Intermediate Manufacturing

    Many 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary)
    • European (Ph. Eur.) and Japanese (JP) Pharmacopoeia standards
    • WHO Prequalification Programme guidelines for APIs

    Typical usage ratio

    • 0.2–2.5% of total reaction mass in multi-step synthesis, with adjustment based on targeted intermediate chain length or steric requirements

    Downstream process integration

    • Introduced at amidation, N-protection, or condensation reaction stages, subjected to in-line quality control/trace impurity monitoring, followed by hydrolysis or further derivatization as required

    Final product types

    • API intermediates (e.g., beta-lactam pre-cursors, antiretroviral intermediates)
    • Bulk pharmaceutical intermediates qualifying for traceability and impurity residuals specifications

    3. Specialty Polymer Modifier Production

    Synthesizers 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

    • ISO 9001:2015 and ISO 14001:2015 for manufacturing and EHS management
    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU) for electrical applications
    • FDA 21 CFR 177.1810 (where applicable for indirect food contact plastics)

    Typical usage ratio

    • 0.3–1.2% by weight based on total monomer mixture, varied according to target polymer grade and end-use performance

    Downstream process integration

    • Added during copolymerization or grafting stage, blended under inert or nitrogen atmosphere, followed by melt extrusion or solution polymerization processes tailored to specific engineering resin architecture

    Final product types

    • Modified polyamides and engineering plastics for automotive components
    • Specialty thermosetting resins for electronics encapsulation
    • High-stability coatings for industrial equipment

    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

    • ISO 9001:2015 and ISO 14001:2015 (chemical production management)
    • Chemical Facility Anti-Terrorism Standards (US DHS, where applicable)
    • REACH Annex II (Safety Data Sheet requirements for fine chemicals in Europe)

    Typical usage ratio

    • 0.7–3% based on total substrate input; formulated according to required steric hindrance and downstream purification threshold

    Downstream process integration

    • Used in amidation, esterification, or catalyst-ligand precursor synthesis steps; charged as reagent in fine chemical batch or semi-continuous reactors under controlled temperature and base catalysis

    Final product types

    • Sterically hindered amines used in light stabilizer production
    • Specialty esters for performance additives
    • Ligands for homogeneous catalyst synthesis

    5. Photoinitiator and UV Stabilizer Component Manufacturing

    Manufacturers 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

    • ISO 9001:2015 (quality systems for specialty chemical production)
    • GMP guidelines for chemical additives (where intended for regulated applications such as packaging or medical devices)
    • REACH compliance for European market entry

    Typical usage ratio

    • 0.4–2.0% depending on photoinitiator type and performance requirement; dosage determined by stoichiometry and compatibility with other initiator system components

    Downstream process integration

    • Introduced in the intermediate coupling or final derivatization stage of photoinitiator or stabilizer synthesis, followed by solvent removal, purification, and performance testing

    Final product types

    • UV-curable ink and adhesive photoinitiators
    • Polymer additive UV stabilizers for plastics and coatings
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