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3'-Aminobenzanilide

    • Product Name 3'-Aminobenzanilide
    • Alias 3'-Amino-[1,1'-biphenyl]-3-carboxamide
    • Einecs 617-089-9
    • 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

    579989

    Cas Number 6147-85-3
    Molecular Formula C13H12N2O
    Molecular Weight 212.25 g/mol
    Iupac Name 3'-Aminobenzanilide
    Appearance Off-white to yellow crystalline powder
    Melting Point 160-163°C
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Smiles NC1=CC(=CC=C1)C(=O)NC2=CC=CC=C2
    Synonyms 3-Amino-N-phenylbenzamide
    Storage Temperature Store at 2-8°C

    As an accredited 3'-Aminobenzanilide 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, sealed with a screw cap, and clearly labeled with "3'-Aminobenzanilide, 25g, for research use only."
    Shipping 3'-Aminobenzanilide is typically shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous material, following relevant regulations. Shipping may require labeling for laboratory chemicals, with temperature and ventilation controls as needed to prevent degradation or accidental exposure during transit.
    Storage 3'-Aminobenzanilide should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it at room temperature, away from incompatible substances such as strong oxidizing agents. Proper labeling and secure storage to prevent unauthorized access or environmental contamination are recommended. Always follow institutional and safety data sheet guidelines.
    Application of 3'-Aminobenzanilide

    Applications of 3'-Aminobenzanilide in Industrial Manufacturing

    3'-Aminobenzanilide is a functional aromatic amide widely used as an intermediate in fine chemical production, most notably in dye synthesis, pigment formulation, polymer additives, and certain specialty coatings. As a direct-manufacturer, we supply this raw material to a limited set of established downstream sectors where it provides proven performance rooted in its amide structure and reactivity profile.

    1. Azo Dye Intermediate for Disperse Dye Manufacturing

    In the synthetic dye industry, 3'-aminobenzanilide acts as a key diazo component during the preparation of disperse dyes for polyester textiles. The unique substituent pattern enables the formation of stable azo linkages, impacting shade depth and resistance performance. Manufacturers directly introduce it into the azo condensation stage after diazotization, tailoring dye chromophores for deep shade textile applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Annex 6 for restricted amines and color fastness)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EU REACH Regulation EC No 1907/2006 (Annex XVII on aromatic amines)
    • GB/T 22864-2009 (Colorants used in textiles – Technical specification)

    Typical usage ratio

    • 15–30% (w/w) of total diazo reactant in the coupling stage; actual proportion depends on target dye molecular structure and desired shade intensity.

    Downstream process integration

    • Direct feed into diazo coupling reactors after nitrosation and neutralization steps, preceding filtration, and drying of the finished dye powder.

    Final product types

    • Disperse dyes for polyester fibers
    • Powder and granule dye formulates for textile printing
    • High-fastness dyes for automotive and industrial textile applications

    2. Pigment Intermediate for High-Performance Organic Pigments

    This material is selected in the synthesis of certain monoazo and polyazo pigment structures, especially for high-chromatic yellow and orange pigments used in plastics and inks. The amide group participates in pigment molecule building, contributing to weather and light fastness. The pigment industry incorporates this intermediate during the base-coupling phase to construct pigment precursors before the post-treatment process.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys – Migration of certain elements, pigments safety)
    • AP(89)1 (Council of Europe Resolution on colorants in plastics)
    • ISO 1248:2006 (Pigments – General test methods)
    • 21 CFR 178.3297 (FDA regulations for colorants in polymers for food contact applications)

    Typical usage ratio

    • 10–22% of total aromatic amine input in pigment synthesis; the percentage is adjusted to control hue angle and pigment crystallinity.

    Downstream process integration

    • Introduced into coupling reaction vessels during aqueous or solvent-based pigment base generation, prior to phase separation and drying.

    Final product types

    • Azo yellow and orange pigments for masterbatch compounding
    • Printing ink colorants for PVC and polyolefin substrates
    • Specialty pigments for automotive coatings and exterior plastics

    3. Chemical Intermediate for Polyimide and Polyamide Additives

    Polymer manufacturers employ 3'-aminobenzanilide in the targeted modification of engineering plastics, specifically to introduce functional moieties in polyimide and high-performance polyamide chains. Its aromatic amide framework facilitates improved thermal stability and mechanical attributes in finished compounds. The intermediate is dosed during prepolymer or copolymerization reactions, followed by melt or solution processing depending on the end-use application.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for specialty plastics)
    • UL 94 (Flammability ratings for plastic materials in devices and appliances)
    • EU RoHS Directive 2011/65/EU (Restriction of hazardous substances in electrical and electronic equipment)
    • ASTM D4066 (Standard Classification System for Nylon Resins)

    Typical usage ratio

    • 1–4 mol% relative to total diamine or dianhydride input, with ratio tailored according to performance property targets and resin viscosity profiles.

    Downstream process integration

    • Reactive blending or direct co-feeding in melt-kneader or polycondensation step of polymer production, upstream of pelletizing and compounding.

    Final product types

    • Modified polyimide films for flexible electronics
    • Polyamide-based engineering plastics for automotive components
    • Thermoplastic masterbatch additives for flame retardancy enhancement

    4. Organic Synthesis Building Block in Pharmaceutical Dye Staining Agents

    The compound functions as a specific intermediate in the production of dyes required for medical diagnostics and histology staining. Its chemical structure is leveraged to improve contrast and binding affinity in tissue and blood analysis. Formulators introduce the material in small quantities during the synthesis of staining agent precursors, enabling subsequent formulation into diagnostic reagent kits.

    Industry compliance standards

    • USP 34/NF 29 (United States Pharmacopeia for dye purity in diagnostics)
    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia 10.0 (Reagents for pharmaceutical use)
    • ISO 13485:2016 (Medical device manufacturing including diagnostics)

    Typical usage ratio

    • 0.5–2.5% (w/w) as precursor feedstock in dye formation reactions for diagnostic formulations, dose adjusted based on final stain performance requirements.

    Downstream process integration

    • Integrated during organic coupling and cyclization stages of dye core building, before post-synthetic purification and QC batch release.

    Final product types

    • Biological tissue and slide stains for clinical pathology labs
    • In vitro diagnostic color reagents in blood analysis kits
    • Colorimetric markers for laboratory research chemicals
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