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2-(4-Bromophenyl)Ethylamine

    • Product Name 2-(4-Bromophenyl)Ethylamine
    • Alias Bromo-β-phenylethylamine
    • Einecs 251-896-9
    • 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
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    Specifications

    HS Code

    645654

    Chemical Name 2-(4-Bromophenyl)ethylamine
    Molecular Formula C8H10BrN
    Molecular Weight 200.08 g/mol
    Cas Number 2142-68-9
    Appearance White to off-white solid
    Melting Point 41-45°C
    Boiling Point 290-292°C (at 760 mmHg)
    Density 1.42 g/cm³
    Solubility In Water Slightly soluble
    Synonyms p-Bromo-phenylethylamine, 4-Bromophenylethylamine, PBA
    Smiles C1=CC(=CC=C1CCN)Br
    Inchi InChI=1S/C8H10BrN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2
    Storage Temperature Room temperature, tightly closed
    Hazard Statements Irritant; may cause eye, skin, and respiratory tract irritation
    Pubchem Cid 5312157

    As an accredited 2-(4-Bromophenyl)Ethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle labeled "2-(4-Bromophenyl)Ethylamine," with hazard symbols, CAS#, lot number, and tightly sealed cap.
    Shipping **Shipping Description:** 2-(4-Bromophenyl)ethylamine is shipped in a tightly sealed, chemically resistant container. The package should be clearly labeled, protected against moisture, and cushioned to prevent damage. Shipping must comply with local and international regulations for hazardous chemicals, including documentation and safety data sheets. Handle with appropriate protective equipment.
    Storage 2-(4-Bromophenyl)ethylamine should be stored in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use. Store in a chemical storage cabinet, preferably one designated for amines or organic chemicals. Proper labelling and secondary containment are recommended to prevent accidental release or exposure.
    Application of 2-(4-Bromophenyl)Ethylamine

    Applications of 2-(4-Bromophenyl)Ethylamine in Industrial Manufacturing

    2-(4-Bromophenyl)Ethylamine serves as a valuable intermediate for specialized synthesis across several industrial sectors. We outline its integration into downstream processes, compliance with sector regulations, practical dosage management, and the specific finished products yielded by each application field.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    This compound forms a key building block in the manufacture of select psychiatric and neurological APIs, particularly those featuring brominated aromatic scaffolds. Manufacturers introduce it during the side-chain assembly or amination step under GMP-controlled environments. The amine facilitates formation of target molecules via reductive amination or as a protected intermediate, ensuring compound purity and regulatory traceability throughout the route.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for intermediates
    • Chinese GMP Standards (NMPA)

    Typical usage ratio

    • Employed at 0.9–1.2 molar equivalents relative to the core API structure. Exact ratio depends on target molecule and process yield optimization. Excess amine may be used to drive reaction completeness, followed by purification.

    Downstream process integration

    • Reacted in controlled-batch vessels during intermediate amination.
    • Incorporated during late-stage diversification for halogenated aromatic drug candidates.
    • Included in solid-phase synthesis for CNS-targeted compounds.

    Final product types

    • Antidepressant active ingredients
    • Antipsychotic raw APIs
    • Pharmaceutical-grade intermediate blocks for further derivatization
    • Neurological disorder drug candidates under clinical development

    2. Agrochemical Synthesis: Herbicide and Insecticide Intermediates

    The molecule provides a functionalized ethylamine handle for constructing advanced agrochemical ingredients, especially those requiring halogenation at the para-position. Agrochemical integrators apply this raw material in the coupling phase, progressing to heterocyclic ring closures or direct acylation to yield potent crop protection molecules. Its reliable reactivity profile ensures consistent output during pilot-to-plants scaleup.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • ISO 9001 for Agrochemical Manufacturing
    • REACH Regulation (EU) No. 1907/2006 for precursor management
    • US EPA registration technical requirements

    Typical usage ratio

    • 0.85–1.1 molar equivalents in combining steps. Range depends on downstream coupling agent efficiency and target impurity profile. Slight excess possible to drive completion in high-throughput manufacturing environments.

    Downstream process integration

    • Employed post-chlorination for nucleophilic substitution
    • Utilized in multi-step synthesis during intermediate stage assembly before final derivatization
    • Fed into continuous flow reactors for scale agro-intermediate formation

    Final product types

    • Brominated phenyl-propanamine-based herbicides
    • Precursor compounds for synthetic insecticides
    • Agro-intermediate stock solutions
    • Technical grade actives for field formulations

    3. Dye and Pigment Intermediate for Specialty Colorants

    Industrial dye developers use this ethylamine derivative as a feedstock for rare brominated colorants. The amine group reacts with aldehyde or acid chlorides, yielding chromophore-rich intermediates vital for textile and plastic dye manufacturing. Stringent QC ensures low trace impurities and batchwise color consistency, supporting high-end application needs for heat-resistant and lightfast pigments.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice
    • OEKO-TEX Standard 100 for input chemical management in textiles
    • ISO 9001:2015 quality systems for dye synthesis
    • REACH Annex XVII restriction compliance

    Typical usage ratio

    • Applied at 1–1.3 equivalents versus core chromogenic intermediate, with the ratio tuned to maximize pigment yield and depth. Higher ratios compensate for side reactions forming non-chromophoric byproducts.

    Downstream process integration

    • Introduced in colorant synthesis after halogenated ring activation
    • Coupled during azo/anthraquinone pigment formation
    • Used in condensation with aldehydes for specialty color saturation

    Final product types

    • Brominated dye intermediates for technical textiles
    • Special effect pigments for plastics
    • Lightfast coloration agents for industrial inks
    • Dye stocks for security and anti-counterfeiting marking

    4. Electronic Chemical Synthesis: Liquid Crystal and OLED Intermediate

    Integrated circuit and display component makers demand this compound for constructing advanced organic electronic materials. With its para-brominated aromatic system, it supports the synthesis of key intermediates in liquid crystals and organic light-emitting diode precursor blocks. The high purity level achieved in-house aligns with stringent electronics QC. The molecule enters Suzuki couplings or sequential amide formation steps, underpinning stable display performance and fine-tuned molecular orientation.

    Industry compliance standards

    • IPC-5704 standards for organic electronic chemicals
    • IEC 62679-3-1 for display raw material input
    • REACH and RoHS (Restriction of Hazardous Substances Directive) for electronics sourcing
    • SEMI International Standards for organic chemical supply

    Typical usage ratio

    • Used at 0.95–1.1 equivalents in coupling or amination pathways. Adjustment guided by LC purity profile and endpoint electrical performance requirements. Lower ratios minimize residual side-products in final devices.

    Downstream process integration

    • Inserted during coupling for mesogenic liquid crystal compound production
    • Reacted in amide-forming steps during OLED material synthesis
    • Included in pre-polymer blends for photonic applications

    Final product types

    • Intermediate layers for active liquid crystal displays (LCDs)
    • OLED precursor materials
    • Specialty electronic polymers
    • Organic thin film transistor additives
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