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Tert-Butyl 3-Aminobenzoate

    • Product Name Tert-Butyl 3-Aminobenzoate
    • Alias Tert-Butyl 3-Aminobenzoate; 3-Aminobenzoic acid tert-butyl ester; NSC 47132; tert-Butyl m-aminobenzoate; 3-(tert-Butoxycarbonyl)aniline
    • Einecs 68610-42-8
    • 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

    455383

    Chemical Name Tert-Butyl 3-Aminobenzoate
    Cas Number 136153-82-1
    Molecular Formula C11H15NO2
    Molecular Weight 193.24 g/mol
    Appearance White to off-white solid
    Melting Point 57-61°C
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Purity Typically ≥98%
    Smiles CC(C)(C)OC(=O)C1=CC(=CC=C1)N

    As an accredited Tert-Butyl 3-Aminobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Tert-Butyl 3-Aminobenzoate, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping Tert-Butyl 3-Aminobenzoate should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Use appropriate packaging to prevent leaks or spills. Follow all local, national, and international regulations for the transportation of chemicals, ensuring clear labeling and documentation for safe and compliant delivery.
    Storage Tert-Butyl 3-Aminobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and sources of ignition. Protect from light and incompatible materials such as strong acids and oxidizing agents. Ensure proper labeling and keep the storage area accessible only to trained personnel. Use appropriate personal protective equipment when handling.
    Application of Tert-Butyl 3-Aminobenzoate

    Applications of Tert-Butyl 3-Aminobenzoate in Industrial Manufacturing

    As a specialist manufacturer of Tert-Butyl 3-Aminobenzoate, we support a select group of industries by providing this key intermediate for downstream synthesis. The following application scenarios reflect established, large-volume sectors where our material enters complex production lines and meets regulatory and quality benchmarks central to commercial operations.

    1. Pharmaceutical Active Pharmaceutical Ingredient Intermediates

    API manufacturers rely on our material as a structurally significant intermediate for the synthesis of various small-molecule drugs, particularly targeted therapeutics in anti-inflammatory and central nervous system categories. The stability conferred by the tert-butyl ester group and amine functionality assists in advanced side-chain constructions during multi-step syntheses, with the product often incorporated before a final deprotection or amidation stage. The choice of this intermediate is dictated by compendial requirements and established synthetic routes, necessitating strict quality assurance at each batch release.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP/NF and Ph. Eur. specifications for intermediates
    • FDA 21 CFR Part 211
    • ISO 9001:2015 for quality management

    Typical usage ratio

    • In multi-step syntheses, 1.1–1.5 molar equivalents relative to the next coupling partner, adjusted according to target yield and downstream conversion requirements.

    Downstream process integration

    • Charged post-initial stage to construct aminobenzoate core, before saponification or amidation toward key intermediates; integrated during protected functional group installation, followed by selective hydrolysis or acylation in primary reactors with real-time in-process controls (HPLC monitoring).

    Final product types

    • Pharmaceutical intermediates for anti-inflammatory agents
    • Building blocks for CNS-active APIs
    • Pain modulation drug precursors
    • Fine chemicals for contract research organizations

    2. Organic Photoinitiator Synthesis

    Chemical companies in the specialty materials sector utilize Tert-Butyl 3-Aminobenzoate to manufacture core fragments for photoinitiators deployed in inks, polymerizations, and UV-cured coatings. The material enters as a nucleophilic aromatic amine reactant that allows targeted diazotization or coupling to functionalize benzene rings for effective UV-light absorption. Producers demand this intermediate in high-purity, non-aqueous formats to ensure reaction efficiency and minimize downstream impurities.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 14001:2015 Environmental Management
    • RoHS Directive 2011/65/EU (where relevant for electronics applications)
    • Customer-specific impurity control specifications (sub-ppm heavy metals and organic residues)

    Typical usage ratio

    • 0.5–3.0% by weight of the total batch, modulated according to batch scale, light absorption target, and final molecular structure requirements.

    Downstream process integration

    • Introduced at the aromatic amination or benzoate esterification stage before conversion to initiator backbone; undergoes coupling or condensation with specific benzophenone or benzoin derivatives in jacketed reactors equipped with UV-protected transfer systems.

    Final product types

    • Free radical photoinitiators for UV-cured coatings
    • Photoactive resins for inkjet and screen printing
    • Photoinitiators for electronics encapsulation materials
    • Oligomeric crosslinker backbones

    3. Agrochemical Synthesis of Herbicide Intermediates

    Major agrochemical enterprises source our product for integration into the synthesis of substituted benzoate herbicides and safeners. Its amine group facilitates specific acylation and ring substitution steps, essential for tailoring the mode-of-action profile of the resulting crop protection molecules. The purity and batch-to-batch consistency of our material underpin quality assurance in final actives destined for regional and international regulatory submissions.

    Industry compliance standards

    • FAO/WHO specification for pesticide manufacturing
    • ISO 17025:2017 analytical laboratory certification
    • European Union Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA pesticide intermediate standards

    Typical usage ratio

    • 1.2–1.8 molar equivalents as a coupling partner, varying by target herbicide structure and overall process yield optimization.

    Downstream process integration

    • Added during selective benzoate derivatization prior to chlorination or alkylation; processed in controlled batch reactors with monitored pH and temperature to minimize unwanted by-products.

    Final product types

    • Precursor compounds for broadleaf herbicide actives
    • Synthetic intermediates for safener formulations
    • Benzoate-derived crop protection agents
    • Bulk actives for finished EC and SC pesticide products

    4. Specialty Polymer Modifier Manufacturing

    Producers of specialty polymers deploy this intermediate for constructing functionalized monomers that introduce amine-reactive sites, supporting the design of high-performance engineering plastics and electronic encapsulants. Its tert-butyl ester offers a removable protecting group during controlled radical or condensation polymerization, with subsequent post-polymerization deprotection enabling site-specific crosslinking or further derivatization.

    Industry compliance standards

    • ISO 9001:2015 quality management for polymer production
    • ASTM D256 for plastic identification
    • RoHS when polymers are destined for electronic devices
    • UL 94 for flammability in engineering plastics (where required)

    Typical usage ratio

    • Between 0.5–2.5% of total monomer feed, optimized for target crosslink density and subsequent reactivity of deprotected groups.

    Downstream process integration

    • Introduced as part of the monomer mixture in pre-polymerization blending; followed by copolymerization in bulk, solution, or emulsion processes; subsequent thermal or acid-mediated deprotection liberates free amines for advanced material functionalization.

    Final product types

    • Engineering thermoplastics with tunable amine side groups
    • High-performance electronic encapsulant resins
    • Reactive hot-melt adhesives
    • Specialty polyamides or polyesters
    Free Quote

    Competitive Tert-Butyl 3-Aminobenzoate prices that fit your budget—flexible terms and customized quotes for every order.

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