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2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One

    • Product Name 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One
    • Alias Aripiprazole
    • 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

    993187

    Iupac Name 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-piperazinyl]phenyl]-2-(1-methylpropyl)-3H-1,2,4-triazol-3-one
    Molecular Formula C24H30N6O2
    Molecular Weight 434.53 g/mol
    Cas Number 87985-55-9
    Appearance White to off-white solid
    Solubility Slightly soluble in water, soluble in organic solvents
    Logp Estimated 3.5 - 4.0
    Synonyms Rilmazafone (prodrug), Rilmazolam derivative
    Chemical Class 1,2,4-Triazolone derivative
    Functional Groups Triazolone, piperazine, methoxyphenyl, alkyl chain
    Structure Type Heterocyclic compound, aromatic substituted

    As an accredited 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle labeled with the chemical name, purity, hazard symbols, batch number, and storage instructions.
    Shipping This chemical, 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One, is shipped in securely sealed containers, compliant with all relevant chemical safety regulations. Packaging ensures protection from light, moisture, and physical damage, with clear hazard labeling and documentation for safe handling and transport under ambient conditions.
    Storage Store 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-piperazinyl]phenyl]-2-(1-methylpropyl)-3H-1,2,4-triazol-3-one in a tightly sealed container, away from direct sunlight, moisture, and incompatible materials. Keep in a cool, dry, and well-ventilated area. Ensure appropriate chemical labeling and restrict access to trained personnel. Follow standard safety protocols for handling and storage of laboratory chemicals.
    Application of 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One

    Applications of 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One in Industrial Manufacturing

    As the original manufacturer of 2,4-Dihydro-4-[4-[4-(4-Methoxyphenyl)-1-Piperazinyl]Phenyl]-2-(1-Methylpropyl)-3H-1,2,4-Triazol-3-One, we dedicate our efforts to serving established downstream manufacturers within regulated technology sectors. In alignment with current industry trends and prevailing quality control protocols, we highlight key application scenarios that reflect authentic, traceable, and compliant end-uses throughout global specialty and advanced chemical manufacturing chains.

    1. Pharmaceutical Intermediate for CNS-Active Small Molecule Synthesis

    This compound functions critically as an advanced intermediate within the multi-step synthesis of certain central nervous system (CNS) modulator APIs, particularly those belonging to piperazine-based triazolone derivatives. Leading pharmaceutical plants employ it during final condensation and cyclization stages to achieve strict molecular purity for subsequent API crystallization. Efficient process controls, inline HPLC, and validation to pharmacopoeial specifications ensure downstream quality and batch-to-batch uniformity for eventual medicinal formulation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Notices
    • EU Guidelines for GMP Part II (API Production)
    • Chinese Pharmacopoeia (when localized)

    Typical usage ratio

    • Generally 0.45–0.60 molar equivalents per final step, adjusted to balance yield and purity during medicinal-grade synthesis; exact ratio subject to route optimization in scale-up.

    Downstream process integration

    • Introduced during penultimate or final condensation stages after core structure assembly, with monitored isolation, recrystallization, and aqueous workup forming part of the validated process flow.

    Final product types

    • Regulated CNS-active pharmaceutical ingredients (APIs)
    • Pre-formulation small molecule blocks for clinical trial material supply
    • Reference standards for pharmaceutical QC labs

    2. Key Component in Custom Fine Chemical Synthesis for Medicinal Chemistry

    Specialty fine chemical producers leverage this triazolone derivative as a building block for the custom synthesis of molecular scaffolds requested in collaborative drug discovery. Its complex aromatic-piperazine moiety supports structural diversification through downstream amination, alkylation, or cross-coupling, meeting the differentiated needs of biotech firms engaged in target validation and hit expansion studies. Fully traceable lot release and documentation are maintained throughout toll production and kilo-lab scale-ups.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for Custom Synthesis
    • Responsible Care® Program for chemical stewardship
    • Material transfer and risk assessment per REACH when shipped to the EU
    • Documentation support aligned with client NDA and CDMO protocols

    Typical usage ratio

    • Variable from 0.25% to 2.0% molar concentration within multi-step sequence, determined by the structural demands of the custom scaffold and target molecule complexity.

    Downstream process integration

    • Fed as a dedicated reactant into solution-phase or solid-phase synthesis cycles, often under inert atmosphere; subsequent cleaving or modification depends on client specs and target framework.

    Final product types

    • Small-molecule intermediates for early-stage medicinal chemistry programs
    • Structure-activity relationship (SAR) analog libraries
    • Analytical standards for CRO/CMO screening platforms

    3. Intermediate for Advanced Agrochemical Active Ingredient Synthesis

    The molecule finds targeted use among agrochemical manufacturers who require it for the preparation of select systemic fungicides and herbicide prototypes. Its chemical structure enhances the development of new active compounds with favorable environmental and safety profiles. Production environments utilize established reaction controls, in-process validation, and adhere to stewardship codes that support crop protection product registration in key agricultural markets.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Quality Control of Pesticides
    • OECD Good Laboratory Practice (GLP) for pesticide development
    • ISO 17025 for analytical method validation in agrochemical analysis
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • Typically 0.30–0.80% by mass in the active synthesis phase, optimized according to downstream conversion efficiency and process safety envelope.

    Downstream process integration

    • Introduced post-core scaffold formation, followed by coupling, oxidation, or further triazolone functionalization in enclosed reactor setups; scale-up runs complete with waste stream management.

    Final product types

    • Experimental fungicides entering field trial assessment
    • Herbicide active ingredient samples for regulatory review
    • Reference substances for residue analysis and environmental safety labs

    4. Intermediate in Specialty Dye and Pigment Chemistry

    Manufacturers developing high-performance pigments and specialty dyestuffs for textile, ink, or polymer coloration applications deploy this triazolone compound to build novel chromophores. Its piperazinyl-functionalized backbone allows for post-condensation modification and integration into colorant molecules that demonstrate customized absorption and fastness characteristics. These processes require strict in-process purity control, colorimetric QC, and traceable records for major brand supply chains.

    Industry compliance standards

    • ETAD Code of Practice for colorant manufacturers
    • OEKO-TEX® Standard 100 for restricted substances
    • ISO 105 Series for colorfastness testing in textiles
    • REACH Annex XVII compliance for pigment composition

    Typical usage ratio

    • Range of 1.5–5.0% by mass in pigment precursor batches; scaling is application specific and based on target chromophore yield and batch color consistency.

    Downstream process integration

    • Entered during the key chromophore coupling steps—either aqueous or solvent-based—prior to pigment precipitation, filtration, and drying into dispersible powder or paste forms.

    Final product types

    • Specialty pigments for high-end textile coloration
    • Custom synthesized dyes for inkjet and digital printing
    • Functional colorants in engineering plastics
    Free Quote

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