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3-(4-Chlorophenyl)Glutaramic Acid

    • Product Name 3-(4-Chlorophenyl)Glutaramic Acid
    • Alias NSC 49152
    • Einecs 629-444-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    690599

    Chemical Name 3-(4-Chlorophenyl)Glutaramic Acid
    Molecular Formula C11H12ClNO3
    Molecular Weight 241.67 g/mol
    Cas Number 1428-95-1
    Appearance White to off-white solid
    Melting Point 164-166°C
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Storage Conditions Store at room temperature, tightly sealed, protected from light
    Inchi InChI=1S/C11H12ClNO3/c12-9-3-1-8(2-4-9)7-10(14)5-6-13-11(15)16/h1-4H,5-7H2,(H,13,15,16)
    Smiles C1=CC(=CC=C1C2CCC(=O)NC2=O)Cl

    As an accredited 3-(4-Chlorophenyl)Glutaramic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 grams of 3-(4-Chlorophenyl)Glutaramic Acid is packaged in a sealed, amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 3-(4-Chlorophenyl)Glutaramic Acid is shipped in securely sealed, chemical-resistant containers to prevent leakage or contamination. Packages are clearly labeled according to regulatory requirements, with relevant safety information. Shipping is conducted via approved carriers under suitable temperature and handling conditions to ensure product integrity and compliance with all applicable chemical transport regulations.
    Storage 3-(4-Chlorophenyl)Glutaramic Acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and direct sunlight. Avoid exposure to moisture and incompatible substances such as strong acids or bases. Proper labeling and compliance with local regulations for chemical storage and handling are essential to ensure safety.
    Application of 3-(4-Chlorophenyl)Glutaramic Acid

    Applications of 3-(4-Chlorophenyl)Glutaramic Acid in Industrial Manufacturing

    As a specialized producer of 3-(4-Chlorophenyl)Glutaramic Acid, we support a diverse group of manufacturers operating in advanced chemical industries. This material is used in several high-value sectors as a key intermediate, influencing the quality, performance, and compliance of downstream products. Below we provide application guidance and technical standards for the major industrial segments utilizing this compound.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use 3-(4-Chlorophenyl)Glutaramic Acid as a strategic intermediate in the multistep synthesis of targeted active ingredients for CNS and metabolic disorder drugs. The molecule’s aromatic-chloride functionality enables controlled reactivity in amide coupling and cyclization steps, supporting structural modification and purity control during API assembly. Process optimization requires precise analytical monitoring to meet international pharmacopoeia requirements, and the material’s batch traceability directly links to the integrity of the API supply chain, ensuring consistency between pilot and commercial scale operations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monograph references for intermediates
    • 21 CFR Part 211 (cGMP requirements in US)
    • European GMP Annex 8 (Supplier Qualification)

    Typical usage ratio

    • 0.5–2 molar equivalents per target API batch (adjusted for route efficiency and yield targets)

    Downstream process integration

    • Enter reaction as an amide-precursor in acid-amine condensation steps of the API multi-stage synthesis
    • Undergoes further derivatization and functional group manipulation prior to API isolation and purification

    Final product types

    • Piperidine and pyrrolidine class CNS drugs
    • Metabolic disorder APIs
    • Experimental pharmaceuticals
    • Clinical trial material

    2. Agrochemical Intermediate Manufacturing

    Industrial agrochemical producers rely on this raw material as an intermediate when preparing targeted herbicide, fungicide, and insecticide actives with chlorinated aromatic groups. The glutarimide moiety supports ring-closure reactions and selective halogenation, serving as a precursor for crop protection substances with enhanced environmental persistence and specific action profiles against pests. Manufacturers maintain strict in-process control to minimize cross-contamination and ensure field safety, processing this intermediate in segregation from other aromatic acids to comply with regulatory audits.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice for pesticides
    • FAO/WHO technical specifications for pesticide actives
    • ISO 9001:2015 for agrochemical synthesis
    • REACH Registration for intermediates (EU)

    Typical usage ratio

    • 5–15% by mass of input batch depending on target molecule’s backbone structure and functionalization requirements

    Downstream process integration

    • Introduced at the amidation or ring-formation stage during synthesis of phenyl-substituted herbicide or insecticide actives
    • Participates in multi-step chlorination, esterification, and crystallization prior to final QC and formulation

    Final product types

    • Chlorinated herbicide technicals
    • Fungicide intermediates
    • Custom insecticidal actives
    • Bulk crop protection chemicals

    3. Specialty Polymer Modifier Production

    Chemical manufacturers in the polymer industry incorporate this compound as a monomeric or chain-terminator agent in engineering plastics that demand modified flexibility, thermal behavior, and chemical resistance. Its aromatic-chloro structure promotes compatibility with polyimide, polyamide, and specialty polyester resins where heat deformation and flame-retarding properties need to be engineered at the molecular level. The material is dosed based on polymerization kinetics and end-use testing, with process validation for each polymer run documented for customer certification requests.

    Industry compliance standards

    • ISO 9001 for plastics manufacturing
    • ASTM D3418 (Thermoplastic polymer characterization methods)
    • UL 94 Flame Test for plastics (applied to specific formulations)
    • RoHS Directive (for restricted elements in electrical/electronic grades)

    Typical usage ratio

    • 1–8% by weight based on polymer feedstock (varies with performance targets and formulation requirements)

    Downstream process integration

    • Charged as an intermediate during melt polymerization or solution polymer build-up
    • Integrated via co-polymerization or as a post-polymerization modifier under controlled temperature schedules

    Final product types

    • High-temperature polyimide and polyester plastics
    • Halogenated engineering resins
    • Plastic granules for flame-retardant films
    • High-resistance molded components

    4. Fine Chemical Synthesis for Research and Custom Synthesis

    Contract research organizations (CROs) and labs engaged in development of specialty chemicals use this building block for the preparation of custom molecules needed for advanced materials, catalyst studies, or pharma-validation reference compounds. The defined chlorophenyl and glutaramic acid groups allow synthetic chemists to program site-selective derivatization and scaffold hopping, with the material’s batch history and analytical specs (such as NMR, GC-MS) linking to compliance records for GLP and validated research use.

    Industry compliance standards

    • GLP Principles for non-clinical research
    • ISO 17025 for analytical testing and documentation
    • Individual institution research governance policies
    • Material safety and handling compliance per country regulations (GHS labeling, SDS management)

    Typical usage ratio

    • 0.2–3 mmol per synthetic sequence or exploratory batch (set according to reaction pathway and downstream molecular target complexity)

    Downstream process integration

    • Added at selective amide/ester formation, halide substitution, or cyclization stages during custom organic syntheses
    • Functionally extended for proof-of-concept molecule creation and analytical method development

    Final product types

    • Pharma research intermediates
    • Advanced organic compounds for material science
    • Analytical reference materials
    • Custom synthesis standards for validation studies
    Free Quote

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