(S)-(+)-N-(2,3-Epoxypropyl)Phthalimide

Epoxypropyl

Product Overview

    • (S)-(+)-N-(2,3-Epoxypropyl)Phthalimide, also known as (S)-Glycidyl Phthalimide, is an exceptionally high-tier chiral heterocyclic building block compound. It is commercially supplied as an off-white to white crystalline powder or fine needles. ProCorBay International supplies highly refined, high-chiral purity (S)-(+)-N-(2,3-Epoxypropyl)Phthalimide to active pharmaceutical ingredient laboratories and premium generic synthesis plants requiring strict, high-precision stereochemical controls.
    • This compound is manufactured through the stereospecific nucleophilic substitution reaction connecting pure potassium phthalimide matrices with optically active (R)-epichlorohydrin or related chiral oxirane pathways, followed by multiple low-temperature crystallization passes to eliminate trace enantiomeric impurities. ProCorBay forces quality audits strictly through advanced specialty biochemical lines featuring high optical rotation data and minimal heavy metal variables.
    • Within advanced modern healthcare manufacturing, this epoxidized phthalimide represents a vital chiral core synthesis piece. It functions as the direct chiral starting material and regulatory predecessor for compounding modern oxazolidinone-class oral anticoagulants—most notably serving as the key synthetic block for Rivaroxaban. The localized oxirane epoxy ring provides a highly active node for regioselective ring-opening reactions, helping developers fix the mandatory (S)-configuration into final blood-thinning drug profiles. ProCorBay provides complete analytical validation records to ensure seamless compliance trails.

Applications

    •  
    • Chiral API Synthesis: Primary starting material utilized to manufacture generic Rivaroxaban lines and advanced oxazolidinone medications.
    • Asymmetric Synthesis: Specialized chiral oxirane linker leveraged for custom enantiomeric candidate mapping.

Benefits

    • High Enantiomeric Excess: ≥ 99.0% (ee) chiral purity guarantees exact molecular orientation for optimized receptor binding.
    • Active Oxirane Ring: Epoxide terminal branch delivers high chemical reactivity for step-efficient amine ring-openings.
    • Low Moisture Content: Strictly controlled hydration margins prevent accidental early oxirane ring hydrolysis.
    • Clean Substituted Profile: Highly purified to eliminate free phthalimide or epichlorohydrin trace remnants.
    • Predictable Crystalline Setup: Uniform physical needle grains guarantee consistent dissolution behavior inside factory chemical reactors.
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Frequently Asked Questions

It designates the specific dextrorotatory optical enantiomer required to build the target therapeutic stereochemistry of medications like Rivaroxaban.

Yes, the active epoxide ring can degrade under intense heat. ProCorBay implements ambient temperature-controlled or insulated shipping channels to avoid this issue.