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2-Acetylbutyrolactone

    • Product Name 2-Acetylbutyrolactone
    • Alias 2-Acetyl-γ-butyrolactone
    • Einecs 216-611-1
    • 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

    231896

    Cas Number 517-23-7
    Molecular Formula C6H8O3
    Molecular Weight 128.13 g/mol
    Iupac Name 5-Acetyl-dihydro-2(3H)-furanone
    Appearance Colorless to pale yellow liquid
    Boiling Point 213-214 °C
    Melting Point -6 °C
    Density 1.17 g/cm³ at 20 °C
    Refractive Index 1.4480 - 1.4520
    Solubility In Water Slightly soluble
    Flash Point 87 °C
    Synonyms 5-Acetyl-2(5H)-furanone

    As an accredited 2-Acetylbutyrolactone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Acetylbutyrolactone is supplied in a 100g amber glass bottle with a tamper-evident cap, labeled with safety information.
    Shipping 2-Acetylbutyrolactone should be shipped in tightly sealed containers, protected from moisture and light. It must be handled according to standard chemical transport regulations, ideally via a reputable courier specializing in hazardous materials (if classified as such). Package with appropriate labeling, cushioning against breakage, and include safety data sheets for safe transit.
    Storage 2-Acetylbutyrolactone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. Keep it separated from incompatible substances such as strong oxidizing agents and acids. Store at room temperature and avoid moisture to prevent hydrolysis. Follow all relevant safety guidelines and local regulations.
    Application of 2-Acetylbutyrolactone

    Applications of 2-Acetylbutyrolactone in Industrial Manufacturing

    2-Acetylbutyrolactone holds an established position as a specialty intermediate in multiple chemical and pharmaceutical value chains. As an original manufacturer with large-scale synthesis capability and full vertical QC, we supply this material to global producers for several high-reliability, process-critical end applications. The scenarios below reflect actual downstream use patterns and confirmed industry practices.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Major drug manufacturers use 2-acetylbutyrolactone within small-molecule synthesis routes aimed at producing pyrrolidone- and pyrrolone-based APIs. Its introduction occurs as a key building block in ring construction steps, supporting precise molecular assembly and controllable impurity profiles. Accurate batchwise integration and cGMP-driven documentation govern each aspect, given the traceability and validation demands for pharmaceutical use.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (US FDA Drug GMP)
    • EU EudraLex Volume 4 Guidelines
    • Chinese Pharmacopoeia/USP/EP for intermediates

    Typical usage ratio

    • 5–20% based on total mass in multistep API synthesis; exact proportion set by target molecule’s synthetic pathway and required yield

    Downstream process integration

    • Enter ring closure or acylation stages after core backbone assembly; handled in closed, validated reactors with in-process impurity monitoring

    Final product types

    • Nootropic APIs (e.g., Piracetam derivatives)
    • Anticonvulsants with lactam scaffolding
    • Central nervous system agent precursors

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Global crop protection chemical producers incorporate 2-acetylbutyrolactone to construct specific lactone and pyrrole segments required in high-activity herbicide and fungicide molecules. Batch documentation and raw material controls are governed by strict agrochemical audit protocols, especially for export-oriented formulations entering the US, EU, and Japan markets.

    Industry compliance standards

    • ISO 9001 quality system for agrochemical manufacturing
    • FAO/WHO technical material specifications
    • EPA (US) and REACH (EU) registration support for active ingredient manufacture

    Typical usage ratio

    • 2–10% per batch, modifiable according to molecular target yield and structure in multi-stage synthesis

    Downstream process integration

    • Used in the intermediate coupling or ring modification phase following raw acyl donor reactions in fine chemical workshops

    Final product types

    • Selective herbicides (e.g., pyrrolone-based formulations)
    • Fungicidal actives for seed treatment or foliar spray
    • Precursor intermediates for post-emergence crop protection APIs

    3. Electronic Chemicals for Photoresist Synthesis

    Manufacturers of advanced photoresist formulations for semiconductor and printed circuit board (PCB) production rely on 2-acetylbutyrolactone as a specialty monomer to construct fine-tuned, low-ash resins. Batch controls require REACH registration and electronics sector traceability for sub-ppb metal contamination and solvent compatibility. End users demand metrologically certified lot releases to align with international microelectronics manufacturing SOPs.

    Industry compliance standards

    • SEMI C94 and SEMI C1 standards for electronic-grade raw materials
    • REACH registration for raw material import to EU
    • RoHS directive for controlled substances in electronics

    Typical usage ratio

    • 0.5–3% by weight in photoactive layer matrix, adjusted for solubility, resin chain growth control, and final resist sensitivity

    Downstream process integration

    • Charged to batch reactors during resin prepolymerization before the addition of diazo sensitizers

    Final product types

    • Positive and negative photoresists for IC lithography
    • Micro-patternable coatings for semiconductor wafers
    • PCB patterning films

    4. Specialty Solvent and Electrolyte Additive in Lithium-ion Battery Manufacturing

    Lithium battery cell manufacturers use 2-acetylbutyrolactone as a functional additive for non-aqueous electrolyte solutions, enhancing cycle stability and reducing solvent degradation, particularly for high-voltage and fast-charging cell chemistries. Integration requires adherence to restricted impurity and moisture thresholds, with process steps adapted for safety and automated doping to ensure reproducibility in large-scale electrode fabrication lines.

    Industry compliance standards

    • IEC 62660-2 for lithium-ion battery safety testing
    • UN38.3 (Transport of Lithium Cells and Batteries)
    • TUV and UL 2580 for battery system safety

    Typical usage ratio

    • 0.2–1.0% by weight in liquid electrolyte blends, modulated based on C-rate, electrode material, and performance targets

    Downstream process integration

    • Injected into electrolyte blending tanks prior to vacuum drying and cell filling under inert atmosphere

    Final product types

    • Cylindrical, pouch, and prismatic lithium-ion cells
    • High-rate discharge batteries for automotive and consumer electronics
    • Rechargeable battery modules for energy storage systems

    5. Fine Chemicals for Dye and Pigment Synthesis

    Specialty pigment and dye producers employ 2-acetylbutyrolactone within advanced chromophore construction, particularly for high-purity lactone- or quinone-based colorants used in textile and plastic coloration. Manufacturers must verify raw material credentials for heavy metal and aromatic amine content, following EU and US textile and plastics additive regulations.

    Industry compliance standards

    • OEKO-TEX 100 toxicological safety
    • EN 71-3 migration of certain elements (toys and textiles)
    • REACH SVHC compliance for pigment ingredients

    Typical usage ratio

    • 3–10% by mass within specialty dye precursor blends, tailored per target chromophore structure and batch size

    Downstream process integration

    • Added to condensation reactions post-nucleophilic aromatic substitution; handled under controlled temperature in jacketed kettles

    Final product types

    • High-performance quinone-based pigments
    • Fluorescent and specialty dyes for synthetic fiber applications
    • Plastic-compatible masterbatches for technical compounding
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