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3-Methylglutaric Anhydride

    • Product Name 3-Methylglutaric Anhydride
    • Alias 3-Methylglutaric anhydride
    • Einecs 249-023-2
    • 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

    730415

    Cas Number 2693-58-9
    Molecular Formula C6H6O3
    Molecular Weight 126.11 g/mol
    Iupac Name 3-Methyloxolane-2,5-dione
    Appearance White to off-white crystalline powder
    Melting Point 70-72°C
    Boiling Point 246°C at 760 mmHg
    Purity Typically >98%
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³
    Storage Temperature Store at room temperature, tightly sealed and dry
    Smiles CC1CC(=O)OC1=O
    Synonyms 3-Methylglutaric acid anhydride
    Hazard Statements Irritant

    As an accredited 3-Methylglutaric Anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g packaging is a sealed amber glass bottle with a white screw cap, clearly labeled "3-Methylglutaric Anhydride, 100g."
    Shipping 3-Methylglutaric Anhydride is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. It should be handled as a hazardous material, following all relevant regulations. Packages are clearly labeled, and transport is conducted with care, protecting from physical damage, heat, and incompatible substances during transit.
    Storage 3-Methylglutaric anhydride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, sparks, and incompatible substances such as water and strong bases. Protect from physical damage and direct sunlight. Proper labelling and access control are essential. Personal protective equipment (PPE) should be used when handling the chemical.
    Application of 3-Methylglutaric Anhydride

    Applications of 3-Methylglutaric Anhydride in Industrial Manufacturing

    3-Methylglutaric Anhydride serves as an essential intermediate for high-value chemical synthesis across key sectors. As the original manufacturer, we supply this compound for well-established industrial applications. Each downstream field requires precise compliance, formulation strategy, and integration for consistent, safe, and efficient production.

    1. Polyimide Film and Resin Precursors

    Engineers select our 3-Methylglutaric Anhydride during the dianhydride stage for specialty polyimide synthesis. Its branched structure modulates polymer properties such as thermal resistance and flexibility, enabling advanced electrical insulation films and resistant coatings. Strict polymer-grade purity applies, given the usage in electronics and aerospace. Formulators adjust the anhydride to diamine ratio to tune film cross-linking density. The material enters after initial diamine selection, dissolves fully in dry aprotic solvents, and reacts under controlled temperature ramps to minimize unintended imide ring cleavage. QC includes residual acid titration and FTIR analysis at imidization endpoints. Downstream extrusion or casting produces thin films or resins for electronic substrate applications.

    Industry compliance standards

    • IPC-4101B for base materials
    • UL 94 V-0 for flame retardancy
    • RoHS/REACH for hazard substances
    • EN 60216 for thermal endurance of insulating materials

    Typical usage ratio

    • 1.00 to 1.02 molar ratio with diamines, adjusted by polymer design
    • Solvent concentration: 10–25% wt/vol solution phase before cyclization

    Downstream process integration

    • Mixing in closed polymerization vessels directly after diamine solution prep
    • Thermal or chemical imidization cycle at 80°C–240°C based on target imide ring integrity
    • Residue QC and viscosity measurement before extrusion/casting

    Final product types

    • Flexible polyimide films for printed circuit boards
    • Resin binders for advanced composite prepregs
    • Coating systems for aerospace components
    • High-temperature electrical insulation tapes

    2. Pharmaceutical Intermediates for Statin Side-Chain Synthesis

    Pharmaceutical manufacturers employ this anhydride as a key building block in the multi-step synthesis of chiral side chains for statin APIs, specifically in the elaboration of HMG-CoA reductase inhibitor derivatives. High-purity, low-moisture material is mandatory to prevent hydrolytic side reactions and facilitate repeatable chiral transformations in strictly controlled batch reactors. Conforming to current GMP, material is screened via HPLC and specific optical rotation tests. Anhydride enters the synthesis post-alkylation or Grignard step, where it reacts with protected alcoholates for side-chain elongation. Reagents and ratios are scaled depending on the intended statin analog and manufacturing size (pilot/industrial). Procedure schedules solvent exchange and in-process pH regulation to maximize yield and chiral purity for downstream hydrolysis and salt formation steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP <791> pH determination for chemical intermediates
    • EP 2.2.24 Optical Rotation for chiral analysis
    • 21 CFR Part 211 process controls (FDA)

    Typical usage ratio

    • 0.95–1.05 molar equivalents relative to the nucleophilic substrate
    • Adjusts for reaction scale and side-chain type

    Downstream process integration

    • Added after core scaffold preparation for side-chain extension
    • Dosed into dry, inert atmosphere reactors under argon/nitrogen
    • pH and temperature maintained within 0.2 pH units and ±1°C
    • Hydrolysis/derivatization follows for final API precursor

    Final product types

    • Lovastatin and simvastatin intermediates
    • Intermediates for atorvastatin and rosuvastatin
    • Chiral acid and ester side chains for bulk statin synthesis
    • Late-stage pharmaceutical intermediates (LSPI)

    3. Specialty Polyester and Polyol Production

    Producers use 3-Methylglutaric Anhydride to introduce controlled branching in custom aliphatic or aromatic polyesters and polyols. This achieves targeted mechanical and degradation profiles in specialty plastics and elastomers. Material enters the melt or solution phase esterification, reacting with polyols such as glycerol, neopentyl glycol, or other diols. Process engineers adjust the anhydride:polyol ratio for MW control and manipulate heating ramps (typically 120–180°C) to drive conversion while minimizing byproduct formation. Analytical QC includes acid number titration and OH value checks post-reaction. All processes follow chemical industry safety guidelines for anhydride systems, including closed-reactor handling and local exhaust ventilation for vapor minimization.

    Industry compliance standards

    • ISO 9001:2015 for QMS implementation
    • REACH Annex XVII (EU) for downstream plastics
    • ASTM D3835 for polyol characterization
    • 21 CFR 177.1680 (US FDA) if intended for food-contact polymers

    Typical usage ratio

    • 0.5–1.2 molar anhydride per mole of total polyol input, tailored for polymer branching
    • Reaction solid content: 30–80% depending on intended viscosity

    Downstream process integration

    • Charged together with co-monomers in heated esterification kettles
    • Byproduct water condensed and removed under vacuum
    • Post-polymerization purification prior to extrusion or molding
    • Hydroxyl/acidity end-group adjustment for next-step compounding

    Final product types

    • Flexible polyester plastics for automotive interiors
    • Branched polyols for specialty polyurethane foams
    • Degradable agricultural film masterbatches
    • Custom thermoplastic elastomers (TPEs)

    4. Corrosion Inhibitor Synthesis for Metalworking Fluids

    Specialty chemical blenders incorporate 3-Methylglutaric Anhydride into the molecular backbone of functionalized polycarboxylate or succinic derivatives for high-performance corrosion inhibitors. These compounds protect ferrous and non-ferrous metals in harsh aqueous environments. The anhydride reacts in post-neutralization with selected amines or through direct ring-opening during multi-step syntheses. Formulators track free anhydride content by potentiometry to avoid excessive acidity in finished inhibitors. Usage must comply with environmental protection regulations when compounds enter water systems. Finished inhibitor product integration takes place during water-miscible metalworking fluid blending, where additives coordinate with metal surfaces to provide anti-corrosive action without excessive foaming or emulsification problems. All systems are designed for compatibility with hydraulic fluids, process lubricants, and high-load machining coolants.

    Industry compliance standards

    • ASTM D4627 for corrosion inhibition
    • OECD 301B biodegradability for environmental acceptance
    • REACH and TSCA notification for finished additives
    • ISO 12922 (lubricants, industrial oils, hydraulic systems)

    Typical usage ratio

    • 10–30% w/w anhydride-derived intermediate in final inhibitor concentrates
    • Dilution in metalworking fluids at 0.5–2% w/w, based on corrosion test results and end-user coolant type

    Downstream process integration

    • Batch-blended post-neutralization with aminated actives in jacketed reactors
    • Integrated into acrylic copolymer synthesis or as a functional carboxylate
    • Final product standardized by passivation and foam suppression checks
    • Complete cooling and filtration before drum filling

    Final product types

    • Corrosion inhibitor packages for cutting and grinding fluids
    • Protective additives for hydraulic oils
    • Anti-corrosive dispersant packages for rolling oils
    • Specialty coolant additives for heat exchangers
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