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5-Aminoisatoic Anhydride

    • Product Name 5-Aminoisatoic Anhydride
    • Alias 5-AIAA
    • Einecs 629-456-2
    • 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

    827056

    Chemicalname 5-Aminoisatoic Anhydride
    Casnumber 3438-27-5
    Molecularformula C8H6N2O3
    Molecularweight 178.15 g/mol
    Appearance Yellow to orange solid
    Meltingpoint 295-298°C (dec.)
    Boilingpoint Decomposes before boiling
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storagetemperature Store at 2-8°C
    Synonyms 5-Aminoisatoic anhydride, 2,1,3-Benzoxadiazole-4-carboxylic acid, 2,1,3-benzoxadiazole-4,7-dione, 5-amino-2,1,3-benzoxadiazole-4,7-dione
    Structuretype Heterocyclic compound
    Ecnumber 222-461-8

    As an accredited 5-Aminoisatoic Anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Aminoisatoic Anhydride, 5 grams, is supplied in a sealed amber glass bottle with a tamper-evident cap and product labeling.
    Shipping 5-Aminoisatoic Anhydride should be shipped in tightly sealed containers, protected from moisture and light. It must be packed according to chemical safety regulations, with proper labeling and documentation. Shipping should comply with local and international guidelines for hazardous materials. Avoid excessive heat and handle with appropriate personal protective equipment.
    Storage 5-Aminoisatoic Anhydride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and direct sunlight. Avoid sources of ignition and incompatible materials such as strong acids and bases. Store at room temperature and label appropriately. Use proper chemical storage cabinets, and handle with suitable personal protective equipment.
    Application of 5-Aminoisatoic Anhydride

    Applications of 5-Aminoisatoic Anhydride in Industrial Manufacturing

    5-Aminoisatoic Anhydride is an intermediate serving critical roles across specialized chemical manufacturing sectors. Its molecular structure supports advanced synthesis routes for value-added compounds in pharmaceuticals, dyes, and functional materials. The following sections outline key industrial application scenarios and integration details for downstream users.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use 5-Aminoisatoic Anhydride as a targeted intermediate in the synthesis of quinazoline-based APIs. Its high reactivity enables direct amination and cyclization steps, supporting efficient routes to antihypertensive, anticancer, and anti-inflammatory agents. Operators employ this compound in multi-step batch or continuous processes, focusing on yield, purity, and regulatory traceability throughout production campaigns.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – 21 CFR Parts 210/211
    • International Council for Harmonisation (ICH) Q7 for APIs
    • USP-NF and EP monographs for related intermediates
    • Regulatory pre-approval requirements (FDA, EMA) for impurity profiles

    Typical usage ratio

    • 0.85–1.05 molar equivalents relative to target API backbone; adjusted per impurity control and process yield optimization

    Downstream process integration

    • Fed into primary synthesis reactors post-hydrolysis and purification; subsequent cyclization and amination steps under controlled temperature and solvent conditions

    Final product types

    • Quinazoline antihypertensive agents
    • Cancer therapeutic actives (e.g., tyrosine kinase inhibitors)
    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Patent-protected custom pharma compounds

    2. High-Performance Dye Stuffs and Pigment Manufacture

    Colorant manufacturers employ 5-Aminoisatoic Anhydride for the synthesis of anthraquinone and quinazolinone dye scaffolds, valued for their strong chromophore development and substrate affinity. This compound enters selective diazotization and condensation reactions, allowing color tunability for specific fiber, leather, or plastics applications. Customers emphasize narrow impurity profiles and batch consistency for regulatory and technical performance.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for registration and safety data
    • ISO 9001:2015 Quality Management for pigment and dye raw materials
    • OEKO-TEX® Standard 100 for restricted substance content in textile dyes
    • EN 71-3 for safety of toy pigments and colorants

    Typical usage ratio

    • 5–20% by weight of total charge in diazotization batches; varies with desired dye concentration and shade depth

    Downstream process integration

    • Enters reaction tank during primary coupling or condensation sequence, immediately prior to pH adjustment and subsequent isolation/precipitation steps

    Final product types

    • Reactive fabric dyes for cellulose and wool
    • High-affinity dispersive pigments for synthetic polymers
    • Specialty inks for industrial and packaging printing
    • Color masterbatches for plastics extrusion

    3. Specialty Agrochemical Intermediate Production

    Agrochemical formulators utilize 5-Aminoisatoic Anhydride as a core building block in synthesizing selective herbicide and insecticide actives, providing heterocyclic skeletons for mode-of-action optimization. Its production-grade consistency enables predictable conversion in high-throughput processes, ensuring batch traceability and environmental compliance requirements for regulated field use products.

    Industry compliance standards

    • FAO/WHO Specifications for active ingredient content
    • ISO 17025:2017 Laboratory Accreditation for QC analysis
    • Authorized active registration under national EPA scope (e.g., EU PPP Regulation, US FIFRA)
    • CLP Regulation (EU) No 1272/2008 Hazard classification

    Typical usage ratio

    • 0.75–1.2 molar equivalents based on total crop protection intermediate yield; adjusted according to desired purity and downstream process sequence

    Downstream process integration

    • Feeds into initial condensation and ring-closure stages, preceding further acylation or alkylation steps in agrochemical precursor synthesis

    Final product types

    • Systemic herbicide actives (e.g., triazolone derivatives)
    • Nematicidal intermediates for soil treatment
    • Plant growth regulator building blocks
    • Pre-emergence weed control agents

    4. Advanced Materials for Functional Polymer Additives

    Materials manufacturers leverage 5-Aminoisatoic Anhydride as a precursor for high-performance polymer additives, particularly for engineering plastics with elevated thermal stability and electrical insulation requirements. Functional group compatibility allows covalent incorporation or grafting, delivering targeted improvements in finished polyimide, polyamide, or epoxy resin systems under controlled mainline production conditions.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in polymer processing
    • RoHS Directive 2011/65/EU for restricted substances in electronic polymer use
    • UL 94 for flammability rating of finished plastics
    • ISO 11357 for polymer thermal analysis (DSC, TGA)

    Typical usage ratio

    • 0.5–5 parts per hundred resin (phr) as a functional comonomer or cross-linker; adjusted for mechanical/thermal property targets

    Downstream process integration

    • Incorporated during prepolymer mixing or solution-polymerization; may undergo in situ conversion in final polymerization/reactor cycles

    Final product types

    • Thermally conductive polymer composites
    • Electrical insulation film for electronics
    • Heat-resistant molding compounds
    • Engineered adhesives and encapsulants for microelectronics

    5. Fine Chemical Synthesis for Research and Diagnostics

    Chemical research laboratories and diagnostic reagent manufacturers employ 5-Aminoisatoic Anhydride in the targeted synthesis of small molecule libraries, fluorescent probes, and fine chemical tools. Its amine and anhydride functionality enables rapid structural diversification during custom compound development and analytical method creation, with QC and batch documentation maintained per laboratory and regulatory requirements.

    Industry compliance standards

    • GLP (Good Laboratory Practice, OECD Principles)
    • ISO/IEC 17025:2017 for analytical testing laboratories
    • Sigma-Aldrich internal quality specifications for custom synthesis
    • Material Safety Data Sheet (MSDS) documentation for laboratory chemicals

    Typical usage ratio

    • Varies from 0.01–0.30 mmol per reaction; scaled to library throughput and analytical compound quantities

    Downstream process integration

    • Added to organic synthesis set-up during nucleophilic substitution or amide coupling steps, frequently under inert or controlled atmosphere

    Final product types

    • Fluorescent labeling reagents
    • Analytical reference standards
    • Functional assay molecules for diagnostics
    • Pharma screening compound libraries
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    Email: sales7@sinochem-nanjing.com

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