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N-(3-Hydroxypropyl)Phthalimide

    • Product Name N-(3-Hydroxypropyl)Phthalimide
    • Alias N-(3-Hydroxypropyl)phthalimide
    • Einecs 249-615-4
    • 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

    861574

    Iupac Name 2-(3-hydroxypropyl)isoindole-1,3-dione
    Common Name N-(3-Hydroxypropyl)phthalimide
    Cas Number 5244-20-4
    Molecular Formula C11H11NO3
    Molecular Weight 205.21 g/mol
    Appearance White to off-white solid
    Melting Point 104-107 °C
    Solubility In Water Slightly soluble
    Density 1.28 g/cm³ (approximate)
    Smiles O=C1NC(CO)CC1=O
    Inchi InChI=1S/C11H11NO3/c13-7-4-8-12-10(14)5-2-1-3-6-11(12)15/h1-3,5-6,13H,4,7H2
    Storage Conditions Keep container tightly closed, store in a dry, cool place

    As an accredited N-(3-Hydroxypropyl)Phthalimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of N-(3-Hydroxypropyl)phthalimide is supplied in a sealed, amber glass bottle with tamper-evident cap and clear labeling.
    Shipping N-(3-Hydroxypropyl)phthalimide should be shipped in tightly sealed, chemically resistant containers to prevent moisture or contamination. Store and transport it away from incompatible materials such as strong oxidizers. Ensure labeling complies with local regulations. Protect from extreme temperatures and handle with appropriate safety measures to minimize exposure during transit.
    Storage Store **N-(3-Hydroxypropyl)phthalimide** in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong acids, bases, and oxidizing agents. Protect from moisture, direct sunlight, and incompatible substances. Clearly label the storage area and ensure quick access to spill cleanup materials and safety equipment. Follow relevant chemical safety guidelines.
    Application of N-(3-Hydroxypropyl)Phthalimide

    Applications of N-(3-Hydroxypropyl)Phthalimide in Industrial Manufacturing

    N-(3-Hydroxypropyl)Phthalimide serves as a specialized intermediate with established downstream integration across select chemical manufacturing sectors. Its molecular structure allows for utility as a reactive modifier or building block for specialty polymerization and fine chemical synthesis, directly enabling enhanced material properties and facilitating regulated production workflows. Our manufacturing experience supports the following core application environments where quality and process specificity are strictly controlled.

    1. Modifier in High-Performance Polyimide Resin Synthesis

    Resin producers introduce N-(3-Hydroxypropyl)Phthalimide into polyimide resin formulations as a chain-modifying agent to achieve targeted flexibility and thermal stability for advanced electronics and aerospace films. Its hydroxyl functionality enables covalent bonding during imidization, directly influencing polymer structure. Dosing varies according to desired film ductility and end-use dielectric requirements, with strict in-line monitoring per resin batch.

    Industry compliance standards

    • IEC 61249-2-21:2021 (for polyimide flexible circuit substrates)
    • ASTM D5213-15 (polyimide resin properties)
    • RoHS Directive 2011/65/EU (hazardous substances in electronics)
    • IATF 16949:2016 (automotive quality management, where relevant)

    Typical usage ratio

    • 0.5–2.5 wt% based on total dianhydride/diamine content; precise dosing adjusted for targeted glass transition temperature or elongation properties

    Downstream process integration

    • Added directly to the polyamic acid prepolymer mixture during initial monomer charging, prior to imidization; incorporated in solvent-based mixing prior to film casting or molding

    Final product types

    • Flexible printed circuit substrates
    • Flexible copper clad laminates
    • High-temperature insulation films
    • Microelectronics insulating layers

    2. Intermediate for Succinimide-Based Pharmaceutical Synthesis

    Pharma manufacturers use N-(3-Hydroxypropyl)Phthalimide as a key intermediate for constructing succinimide rings in select anticonvulsant or central nervous system APIs. The raw material’s phthalimide core enables clean N-deprotection, facilitating downstream substitution with minimal byproducts. Dosage optimization ensures precise stoichiometry and limits impurities in the synthesis of clinical-grade intermediates.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF (where applicable for excipients and intermediates)
    • EMA Guideline on starting materials for chemical APIs
    • ISO 9001:2015 (pharma production process quality)

    Typical usage ratio

    • Stoichiometric addition (typically 1 mol equivalent relative to alkyl halide or amine reactant); excess adjusted to drive reaction to completion, based on API route efficiency

    Downstream process integration

    • Charged as a starting imide in the protected amine synthesis step, followed by N–O deprotection and coupled condensation; utilized during step-growth and recrystallization in GMP facility reactors

    Final product types

    • Succinimide active pharmaceutical ingredient intermediates
    • Research-grade CNS drug precursors
    • Clinical batch active intermediates

    3. Additive for Epoxy Resin Curing Optimization

    Epoxy manufacturers select N-(3-Hydroxypropyl)Phthalimide as a latent curing agent to extend pot-life and manage cure kinetics in high-temperature casting or coating applications. Its balanced nucleophilicity enables a controlled co-curing mechanism, leading to improved final crosslink density without compromising storage stability or viscosity.

    Industry compliance standards

    • UL 94 (Flammability of plastic materials for parts in devices and appliances testing)
    • EN 45545-2:2020 (Fire protection in railway vehicles)
    • REACH Regulation (EC 1907/2006) compliance

    Typical usage ratio

    • 1.0–3.0 phr (parts per hundred resin) depending on desired gel time and target Tg; increased proportion for slower cure, reduced for faster throughput

    Downstream process integration

    • Dispensed into pre-mixed resin just before application, after main epoxy and hardener blending; homogeneous distribution achieved by low-shear dispersion equipment

    Final product types

    • Electronic component encapsulants
    • Adhesive formulations for high-temperature assembly
    • Structural composite prepregs
    • Industrial floor coatings

    4. Reactive Intermediate for Plasticizer Manufacture

    Specialty plasticizer producers incorporate N-(3-Hydroxypropyl)Phthalimide in downstream esterification or etherification routes, targeting flexible phthalate alternative plasticizers with improved polarity and migration resistance. Its selective reactivity enables synthesis of hydroxypropyl-terminated esters tailored for thermoplastics and elastomers while maintaining regulatory compliance.

    Industry compliance standards

    • EU Regulation 10/2011 (plastics intended to contact food)
    • FDA 21 CFR 177.2600 (elastomeric articles for repeated use)
    • ISO 9001:2015 (plasticizer industry QC)

    Typical usage ratio

    • ~1.2–1.5 molar equivalents for mono-ester formation; excess can be used for bifunctional derivatives, adjusted to limit unreacted hydroxyl content

    Downstream process integration

    • Reacted in heated, catalyzed esterification reactors following raw phthalic anhydride feeding; final product often distilled or vacuum-stripped for high purity

    Final product types

    • Flexible PVC compounders’ high-stability plasticizers
    • Elastomer additives for wire and cable insulation
    • Food contact-compliant softeners

    5. Raw Material for Waterborne Polyurethane Synthesis

    Water-based polyurethane producers utilize this phthalimide derivative as a hydrophilic chain extender, enhancing molecular miscibility and mechanical properties in compliant coatings. Introduced during prepolymer or dispersion phases, its reactivity provides selective chain termination for more controlled crosslinking, optimizing tack and film integrity for regulated markets.

    Industry compliance standards

    • GMP ISO 22716:2007 (coating production for regulated markets)
    • REACH Regulation (EC 1907/2006)
    • Directive 2004/42/EC (VOC limits for paints and varnishes)

    Typical usage ratio

    • 0.8–3.0 wt% on total isocyanate content, based on desired hydrophilicity and molecular weight distribution; ratio fine-tuned for gloss or abrasion resistance

    Downstream process integration

    • Dosed into aqueous prepolymer dispersion after emulsification and neutralization; participates in chain extension alongside diamines or polyols in a controlled reactor system

    Final product types

    • Waterborne polyurethane automotive coatings
    • High-performance textile binder emulsions
    • Regulated packaging adhesives
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