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3-Amino-2-Bromo-5-Chloropyridine

    • Product Name 3-Amino-2-Bromo-5-Chloropyridine
    • Alias 3-Amino-5-chloro-2-bromopyridine
    • Einecs 674-996-6
    • 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

    169347

    Productname 3-Amino-2-Bromo-5-Chloropyridine
    Casnumber 884494-25-5
    Molecularformula C5H4BrClN2
    Molecularweight 223.46 g/mol
    Appearance Off-white to light yellow solid
    Meltingpoint 60-64°C
    Purity Typically ≥97%
    Solubility Soluble in organic solvents such as DMSO and DMF
    Smiles Nc1nccc(Cl)c1Br
    Inchi InChI=1S/C5H4BrClN2/c6-4-2-1-3(7)5(8)9-4/h1-2H,8H2
    Storageconditions Store in a cool, dry place, tightly sealed
    Synonyms 3-Amino-5-chloro-2-bromopyridine

    As an accredited 3-Amino-2-Bromo-5-Chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Amino-2-Bromo-5-Chloropyridine, 5g: Supplied in a sealed, amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Shipping 3-Amino-2-Bromo-5-Chloropyridine is shipped in tightly sealed containers, compliant with chemical safety regulations. It must be protected from moisture and incompatible substances during transit. Shipping typically requires labeling as a hazardous material, with accompanying safety data sheets, and is handled by certified couriers specializing in chemical transportation to ensure safe and legal delivery.
    Storage 3-Amino-2-Bromo-5-Chloropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. It should be kept at room temperature and protected from moisture and ignition sources. Proper chemical labeling and secondary containment are recommended to prevent accidental spills or exposure.
    Application of 3-Amino-2-Bromo-5-Chloropyridine

    Applications of 3-Amino-2-Bromo-5-Chloropyridine in Industrial Manufacturing

    As the original manufacturer of 3-Amino-2-Bromo-5-Chloropyridine, we supply this specialty intermediate to chemical industries demanding traceable compliance, process transparency, and consistent batch quality. Below we detail the principal downstream uses based on factual industrial practice, with scenario-specific information on regulatory context, usage levels, processing steps, and resulting product types.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    3-Amino-2-Bromo-5-Chloropyridine serves as a key heterocyclic synthon in the preparation of certain antihypertensive active pharmaceutical ingredients (APIs), especially those involving pyridine-modified small molecules in modern cardiovascular pipelines. Major API manufacturers use it for ring functionalization in late-stage synthesis processes, with precise formulation determined by process yields and impurity controls demanded by finished drug regulatory submission.

    Industry compliance standards

    • ICH Q7: GMP for Active Pharmaceutical Ingredients
    • USP/NF Monographs for relevant APIs
    • European Pharmacopoeia (Ph. Eur.)
    • FDA DMF (Drug Master File) submission requirements

    Typical usage ratio

    • 5–15% by molar equivalent within multi-step reaction trains; adjusted by targeted step yield and impurity profile of the API carried through post-synthesis purification

    Downstream process integration

    • Integrated as a nucleophilic aromatic substitution reactant for core ring derivatization, followed by reduction, cyclization, or halide exchange depending on API structure; precise loading based on batch route design from development through scaled production

    Final product types

    • Antihypertensive APIs such as pyridine-derived angiotensin receptor blockers or calcium channel modulator intermediates
    • Regulatory submission-grade intermediates for further contract synthesis

    2. Agrochemical Active Ingredient Synthesis

    In large-scale crop protection chemistry, this compound functions as a tailored halopyridine building block for the synthesis of advanced herbicidal and insecticidal actives. Agrochemical companies rely on its reactivity to introduce complex substitution patterns into the pyridine core, forming precursors for actives with improved target selectivity and resistance management.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 Quality Management
    • REACH Regulation (EC) No 1907/2006 when manufactured or imported into the EU
    • GLP (Good Laboratory Practice) for registration study materials

    Typical usage ratio

    • 2–8% by weight in active ingredient synthesis batch; proportion varies by activity window of final molecule and desired step conversion rate during halogen exchange or amination

    Downstream process integration

    • Introduced during key heterocycle assembly and functionalization, typically as the initial reactant for cross-coupling or amine protection chemistry, followed by subsequent purification for technical-grade actives or formulated concentrates

    Final product types

    • Herbicide and insecticide actives containing substituted pyridine motifs
    • Pre-formulated technical concentrates for post-emergence crop protection

    3. Specialty Dye and Pigment Intermediate

    Fine chemical and pigment manufacturers use 3-Amino-2-Bromo-5-Chloropyridine for selective synthesis of specialty disazo and metal-complex dyes, targeting high-performance sectors such as digital printing and polymer coloration. Its ring-substitution profile provides stable chromophore generation under high-temperature or high-light environments.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile safety
    • EN 71-3 (Toy Safety: migration of certain elements)
    • DIN EN ISO 13320 for pigment particle size analysis
    • European Union REACH SVHC screening

    Typical usage ratio

    • 1–4% by weight in chromophore formation steps; adjusted based on final pigment load, purity of color required, and downstream formulation incompatibilities

    Downstream process integration

    • Employed in early-stage coupling reactions to construct azo bonds or as the halogenated aromatic nucleus before complexation with transition metals, followed by crystallization and post-purification milling

    Final product types

    • Disazo textile dyes for polyester fiber coloration
    • Lightfast pigments in inkjet printing formulations

    4. Advanced Electronic Material Chemical Synthesis

    Emerging electronic material manufacturers adopt this pyridine derivative during the design of highly functionalized heterocyclic motifs, primarily as a controlled precursor for organic semiconductors and photostabilizers. The well-defined halogen and amine positions facilitate precise doping or modification steps oriented toward display, OLED, and organic photovoltaic end uses.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-Free Electronic Materials
    • RoHS Directive 2011/65/EU for restricted substances
    • ISO 9001:2015 for electronic-grade chemicals
    • IPC-4101B for base materials control

    Typical usage ratio

    • 0.5–3% by molar input within functional organic synthesis; precise dose modified by conductivity requirements and degree of halogenation allowed in final device layers

    Downstream process integration

    • Deployed during the assembly of precursor libraries by solution-phase or solid-phase heterocycle formation, feeding directly into monomer or oligomer synthesis for organic transistor or emission layer manufacturing

    Final product types

    • Organic semiconductors for flexible displays and lighting
    • Photostabilizer compounds for next-generation optoelectronic coatings
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