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5-Bromo-3-Methoxypyrazin-2-Ylamine

    • Product Name 5-Bromo-3-Methoxypyrazin-2-Ylamine
    • Alias 2-Amino-5-bromo-3-methoxypyrazine
    • Einecs 841-631-5
    • 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

    383398

    Chemical Name 5-Bromo-3-Methoxypyrazin-2-Ylamine
    Cas Number 356783-66-3
    Molecular Formula C5H6BrN3O
    Molecular Weight 204.03
    Appearance Solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Temperature 2-8°C
    Synonyms 5-Bromo-3-methoxy-2-pyrazinamine
    Smiles COC1=NC(N)=NC(Br)=C1
    Inchi InChI=1S/C5H6BrN3O/c1-10-4-3(6)2(7)8-9-5(4)10
    Usage Research and chemical synthesis

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

    Packing & Storage
    Packing White, sealed glass vial containing 5 grams of 5-Bromo-3-Methoxypyrazin-2-Ylamine, labeled with chemical name, purity, and hazard symbols.
    Shipping 5-Bromo-3-Methoxypyrazin-2-Ylamine is shipped in tightly sealed, chemical-resistant containers, clearly labeled per regulatory requirements. It is transported at ambient temperature with appropriate documentation. The package includes safety data sheets, and it complies with all hazardous material handling protocols to ensure safe and secure delivery.
    Storage 5-Bromo-3-Methoxypyrazin-2-Ylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from heat, moisture, and direct sunlight. Store away from incompatible substances, such as strong oxidizers. Ensure proper labeling, and keep storage area equipped for handling spills or leaks, following all appropriate safety and environmental regulations.
    Application of 5-Bromo-3-Methoxypyrazin-2-Ylamine

    Applications of 5-Bromo-3-Methoxypyrazin-2-Ylamine in Industrial Manufacturing

    As a specialized manufacturer of 5-Bromo-3-Methoxypyrazin-2-Ylamine, we supply this high-purity chemical intermediate for inclusion in advanced synthesis routes across defined industrial sectors. This page outlines the material’s well-established downstream uses in pharmaceutical, agrochemical, and specialty chemical production, with a focus on practical integration, compliance, formulation ratios, and finished goods output by our customers.

    1. Pharmaceutical Intermediates for Oncology APIs

    Major drug substance manufacturers source our material as a key heterocyclic intermediate for assembling active pharmaceutical ingredients (APIs) in tumor therapy research and production. It reacts at controlled steps during the synthesis of pharmaceutical pyrazine derivatives, where strict trace metal, residual solvent, and stereochemical specifications must be met according to global regulatory frameworks.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs)
    • EDQM CEP and EU GMP Part II requirements for synthetic intermediates
    • Chinese Pharmacopoeia (ChP) reference for impurity control

    Typical usage ratio

    • Utilized in multistep synthesis at 1.5% – 4% molar equivalent relative to target pyrazine-bearing intermediates; adjusted based on pathway efficiencies and contamination allowance.

    Downstream process integration

    • Charged into reactor vessel during nucleophilic substitution or palladium-catalyzed amination, typically after initial halogenation. Integration occurs under inert atmosphere, with strict batch record for traceability.

    Final product types

    • Anti-cancer drug substances (API) for targeted chemotherapeutic formulations
    • Research-grade reference compounds for oncology screening
    • Key intermediates for small-molecule kinase inhibitors

    2. Building Block in Agrochemical Synthesis

    Producers of advanced crop protection agents incorporate this material as a nitrogen-rich building block for constructing active ingredients with selective herbicidal or fungicidal activity. Its reactivity enables downstream modification and functionalization essential for achieving desired bioactivity profiles, under rigorous process safety management in full-scale synthesis.

    Industry compliance standards

    • ISO 9001:2015-certified Quality Management System for agrochemical production
    • OECD Guidelines for the Testing of Chemicals (applicable to active ingredient precursors)
    • Chinese GB 2763: National Maximum Residue Limits for Pesticides in Food
    • FAO/WHO Guidelines for the registration and evaluation of pesticide intermediates

    Typical usage ratio

    • Incorporated at 2% – 6% weight basis of total reaction mixture, depending on the scale of active ingredient batch and conversion yield in pyrazine ring derivatization.

    Downstream process integration

    • Introduced during ring closure reactions, following initial halogen shuffle stages. Fed via metered addition for precise stoichiometry in large-scale, DCS-monitored production lines.

    Final product types

    • Selective herbicide technical concentrates
    • Systemic fungicide technical materials
    • Intermediates for pyrazine-based insecticidal actives

    3. Precursor for Specialty Chemical Synthesis in Electronics

    Producers of specialty heterocyclic compounds for electronics and OLED (organic light-emitting diode) industries utilize our raw material as a fundamental precursor in engineering nitrogen–bromine substituted pyrazine motifs, central to the synthesis of emitting or charge-transport layers for high-performance organic semiconductors.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • REACH Regulation (EC) No. 1907/2006 for chemical safety information
    • Internal customer QC/QA protocols for impurity profiling and purity assurance to 99.5%+
    • IPC/JEDEC J-STD-033 standards for handling and packaging moisture-sensitive materials

    Typical usage ratio

    • Charged at 0.8% – 2% by weight in the key coupling or cyclization stage, responsive to batch throughput and desired molecular architecture.

    Downstream process integration

    • Dosed during Suzuki or Buchwald–Hartwig cross-coupling for assembling pyrazine–aryl linkages, prior to end-group protection and purification stages. Automated tracking ensures batch consistency and regulatory documentation.

    Final product types

    • OLED emitter and host molecules
    • Organic semiconducting materials for thin-film transistors
    • Heterocyclic ligands for advanced photolithography photoresists

    4. Intermediate for Fine Chemical Scents and Flavors

    Certain flavor and fragrance manufacturers with established R&D programs employ this chemical as a pyrazine core intermediate for the synthesis of specialty aroma compounds with defined flavor notes used in low-ppm formulations for food or fragrance applications. Material handling and traceability follow requirements for food contact sub-ingredients and output assessments to exclude non-permitted byproducts.

    Industry compliance standards

    • IFRA Code of Practice for the Manufacture of Fragrance Materials
    • FEMA GRAS status for intermediates-involved synthetic flavors (where applicable)
    • ISO 22000:2018 Food Safety Management System for ingredient manufacturers
    • US Food Chemical Codex for control of permitted flavor precursor residues

    Typical usage ratio

    • Used at trace levels, 0.05% – 0.18% weight/weight, relative to final pyrazine flavor or aroma production batch, with adjustments based on sensory panel threshold assessments and regulatory compliance for residuals.

    Downstream process integration

    • Integrated into controlled small-scale batch reactors during heterocyclic modification steps, followed by purification, analytical confirmation, and dilution prior to formulation into food-compatible flavoring compounds.

    Final product types

    • Pyrazine-based flavoring agents for processed foods
    • Aroma chemicals for perfumery and air care formulations
    • Concentrated scent compounds for beverage industry applications
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