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2-Bromo-4-Tert-Butylaniline

    • Product Name 2-Bromo-4-Tert-Butylaniline
    • Alias 2-Bromo-4-(tert-butyl)aniline
    • Einecs 617-041-9
    • 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

    543168

    Chemical Name 2-Bromo-4-tert-butylaniline
    Cas Number 183658-65-5
    Molecular Formula C10H14BrN
    Molecular Weight 228.13
    Appearance Light yellow to brown solid
    Boiling Point 332.7°C at 760 mmHg
    Melting Point 36-39°C
    Density 1.35 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Temperature Store at 2-8°C
    Synonyms 4-tert-Butyl-2-bromoaniline
    Smiles CC(C)(C)C1=CC(=C(C=C1)N)Br
    Inchi InChI=1S/C10H14BrN/c1-10(2,3)7-4-5-8(12)9(11)6-7/h4-6H,12H2,1-3H3

    As an accredited 2-Bromo-4-Tert-Butylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Bromo-4-tert-butylaniline, sealed with a screw cap, labeled with hazard and chemical details.
    Shipping **Shipping Description:** 2-Bromo-4-tert-butylaniline should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with relevant chemical transportation regulations. Label packages appropriately with hazard information, and ensure shipment via authorized carriers for chemicals. Handle with care to avoid breakage, spills, or chemical exposure during transit.
    Storage 2-Bromo-4-tert-butylaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat sources and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Ensure the storage area is equipped for handling hazardous chemicals, and label the container clearly to prevent accidental misuse or contamination.
    Application of 2-Bromo-4-Tert-Butylaniline

    Applications of 2-Bromo-4-Tert-Butylaniline in Industrial Manufacturing

    2-Bromo-4-Tert-Butylaniline is a specialized aromatic amine valued across several chemical industry segments for its selectivity in synthesis, reactivity in coupling reactions, and robust substitution profile. We support various industrial partners with direct supply into formulated products and downstream intermediates, enabling precise functionalization and compliance within demanding sectors.

    1. Pharmaceutical Intermediate Synthesis

    This compound serves as a targeted intermediate for custom pharma syntheses, particularly in small-molecule research and commercial API routes involving brominated aromatic amines. Contract manufacturing organizations employ it at the earliest halogenation or amination stage for building drug cores, as well as in late-stage modifications for structure–activity optimization. Our customers integrate this input for the preparation of kinase inhibitors, CNS drug candidates, and other tailored molecules where ortho substitution is essential for biological activity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (cGMP requirements for finished pharmaceuticals)
    • ISO 9001:2015 (Supply chain quality system)
    • Certificate of Analysis (impurity profile as per customer pharma specs)

    Typical usage ratio

    • 10–40% molar feed for key coupling and cyclization steps, adjusted per API process mass intensity and yield optimization

    Downstream process integration

    • Charged in batchwise or continuous bromination and Buchwald-Hartwig amination reactions
    • Used as the primary amine feedstock for heterocycle formation
    • Added post-purification to ensure impurity thresholds match API requirements
    • Integrated upstream to maximize shelf stability and meet shelf-life demands of sensitive actives

    Final product types

    • Small-molecule drug intermediates (protected anilines, aminopyridines)
    • Commercial active pharmaceutical ingredients (AKT inhibitors, brominated CNS agents)
    • Medicinal chemistry library candidates
    • Custom research tool compounds

    2. Agrochemical Active Ingredient Building Block

    Process development laboratories in the crop protection market source this material as an arylamine scaffold for construction of herbicides and fungicide actives containing tert-butyl or bromo-modified aromatic rings. It enters the harmonized pipeline for multi-step synthesis of new-generation agrochemical actives where positional halogenation supports controlled degradation and residue limits. Our downstream partners rely on strict control of ortho-para isomer ratios throughout sulfonation and acylation sequences.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 for accredited test method validations
    • EU REACH Annex XVII (Registration, Evaluation and Authorization of Chemicals)
    • OECD Guideline No. 107 (Partition Coefficient requirements)

    Typical usage ratio

    • 15–35% based on synthesis stage and targeted molecular architecture; adjusted for environmental fate testing and scalability

    Downstream process integration

    • Introduced as an aryl segment in nucleophilic aromatic substitution and coupling reactions
    • Role in side-chain installation and stabilization through controlled temperatures
    • Monitored for conversion purity before bulk formulation into granular or emulsifiable concentrates
    • Batch tracked with retention samples for product recall compliance

    Final product types

    • Brominated herbicides and fungicides (e.g., triazole and anilide-based actives)
    • Formulated crop protection solutions for field application
    • Stabilized SC (suspension concentrate) intermediates
    • Reference standards for residue analytics

    3. Dye and Pigment Intermediate Manufacturing

    Specialty pigment and dye manufacturers use this raw material to design select azo and anthraquinone structures where electron-donating tert-butyl substitution regulates shade and solubility. It forms the aniline base for diazotization and subsequent metal complex formation, which imparts lightfastness and substrate binding in textile and plastics coloration. We supply direct to pigment blenders who monitor salt formation and particle size as critical control points.

    Industry compliance standards

    • Oeko-Tex Standard 100 (Residue and impurity rules for textiles)
    • EN 71-3:2019 (Safety of Toys – migration of certain elements)
    • ETAD Risk Assessment Guidelines
    • ISO 14001 (Environmental management for pigment operations)

    Typical usage ratio

    • 22–30% of aromatic feedstock total input, modulated for batch size, color strength, and desired fastness profile

    Downstream process integration

    • First charged for diazotization to create stable diazonium salt intermediates
    • Reacted with coupling agents for pigment backbone assembly
    • Filtered and purified before blending into paste or granulated concentrate forms
    • QA batch release after particle size and dispersibility testing

    Final product types

    • High-performance organic pigments (red and yellow shades for plastics)
    • Direct dyes for cellulose fibers
    • Special application inks for printing and packaging
    • Seed colorants and non-contact textile dyes

    4. Electronic and Specialty Polymer Synthesis

    Our material supports advanced polymer syntheses where para-brominated anilines enable polymer chain extension, cross-linking, or tailored conductivity properties. It is entered into Grignard or Suzuki coupling routes to produce high-purity specialty monomers for electroluminescent device manufacture, especially in OLEDs and functional resists. Downstream processors monitor for residual bromine and adapt purification to avoid device contamination.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics)
    • ISO 9001:2015 for electronic chemical supply chain
    • IPC-4101 standards for base materials in PCBs
    • JIS C 5016 (Photoconductor material standards)

    Typical usage ratio

    • 8–25% of monomer system input, adjusted for solvent compatibility and desired physical properties of the final polymer

    Downstream process integration

    • Used in step-growth polymerizations and precursor functionalization stages
    • Integrated before chain extension for electrical or barrier properties
    • Monomer purification prior to melt blending and extrusion
    • Residual monitoring to ensure polymer uniformity and device performance

    Final product types

    • OLED material monomers and intermediates
    • Photoresist chemicals for microelectronics
    • Functional polymers for specialty coatings
    • Electronic encapsulants and dielectrics
    Free Quote

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