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2-Bromo-4-Fluorobenzaldehyde

    • Product Name 2-Bromo-4-Fluorobenzaldehyde
    • Alias 2-Bromo-4-fluorobenzalhyde
    • Einecs 841-813-7
    • 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

    616138

    Product Name 2-Bromo-4-Fluorobenzaldehyde
    Cas Number 85118-99-0
    Molecular Formula C7H4BrFO
    Molecular Weight 203.01 g/mol
    Appearance White to off-white solid
    Melting Point 49-51°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Smiles C1=CC(=C(C=C1F)Br)C=O
    Inchi InChI=1S/C7H4BrFO/c8-7-3-5(4-10)1-2-6(7)9
    Storage Conditions Store in a cool, dry place, protected from light and moisture

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

    Packing & Storage
    Packing Amber glass bottle, sealed with a screw cap, labeled with hazard symbols. Contains 25 grams of 2-Bromo-4-Fluorobenzaldehyde powder.
    Shipping 2-Bromo-4-Fluorobenzaldehyde is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. The chemical is transported according to relevant regulations for hazardous materials, usually under cool, dry conditions. Appropriate labeling and documentation accompany the package, and only qualified personnel should handle receiving and unpacking.
    Storage 2-Bromo-4-Fluorobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Handle with appropriate personal protective equipment and store according to local regulations for hazardous chemicals. Keep the container clearly labeled and avoid excessive heat.
    Application of 2-Bromo-4-Fluorobenzaldehyde

    Applications of 2-Bromo-4-Fluorobenzaldehyde in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Bromo-4-Fluorobenzaldehyde for several critical value chains, where it functions as a key intermediate to enable advanced molecule synthesis. Below we detail its principal industrial application segments, with a focus on regulatory adherence, formulation benchmarks, production process roles, and the resulting end-use products in global manufacturing.

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

    Pharmaceutical companies integrate this compound into multi-step processes to build complex heterocyclic scaffolds, especially within the development of selective kinase inhibitors and other oncology APIs. Immediate downstream processes involve condensation, cyclization, and reductive amination, where the aldehyde moiety provides essential reactivity. Its purity and traceability must align with pharmaceutical regulatory expectations, as the intermediate impacts impurity profile control for final APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs (for final APIs)
    • US FDA 21 CFR Part 211 (where integrated in US-bound API supply chains)
    • China GMP (for domestic or export-oriented drug manufacturing)

    Typical usage ratio

    • Ranges from 0.6 to 1.4 molar equivalents relative to main condensation partners, depending on the specific API synthetic route; adjustments reflect impurity controls and batch scale.

    Downstream process integration

    • Serves as an early-step aldehyde intermediate, routinely introduced after initial halogenation or fluorination steps in custom synthesis, leading directly to cyclization or Grignard-type transformations in pharmaceutical chemical plants.

    Final product types

    • Targeted oncology drug APIs (e.g., kinase inhibitor scaffolds)
    • Specialty heterocyclic compounds for further API elaboration
    • Reference standards for pharmaceutical R&D

    2. Agrochemical Active Ingredient Manufacturing

    In the agrochemical sector, downstream producers use this material as a core building block during the synthesis of fluorinated and brominated herbicide actives. Its controlled aldehyde reactivity supports selective condensation with other aromatic or nitrogenous compounds, minimizing formation of isomers that complicate purification. Formulation engineers tailor its dosage to prevent undesirable by-products while complying with product label restrictions in various markets.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EPA 40 CFR Part 158 (US pesticide registration technical requirements)
    • REACH Regulation EC 1907/2006 (for EU market access)
    • ISO 9001:2015 (required by multinational agrochemical groups)

    Typical usage ratio

    • 0.2–0.8% by weight in the overall precursor mixture, dependent on batch yield and downstream reaction optimization, taking into consideration conversion rates and active ingredient potency regulation.

    Downstream process integration

    • Acts as a core aldehyde intermediate, introduced at the aromatic functionalization stage before coupling reactions that form the key agrochemical active backbone; downstream processing includes condensation, reduction, and halogen-exchange steps.

    Final product types

    • Fluorinated and brominated herbicide active ingredients
    • Precursor compounds for insecticide and fungicide synthesis
    • Technical concentrates for further formulation into EC, SC, or WG pesticide products

    3. Fine Chemical Development for Dye & Pigment Intermediates

    Manufacturers involved in the synthesis of specialty pigments utilize this aldehyde compound to generate tailored colorants with enhanced photostability and specific light absorption profiles. Its dual halogenation pattern reduces background coloration and influences chromophore development in azo and anthraquinone dye systems. Usage levels must balance optimal yield with final pigment purity required for electronics or automotive applications.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidance for Dye Intermediates
    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • DIN EN 71-3 (colorant safety for toy and consumer product applications)
    • REACH Regulation EC 1907/2006 (mandatory for pigment use in the EU)

    Typical usage ratio

    • 0.5–1.5% per batch, calculated on a pigment mass basis, with precise addition rate determined by desired absorption spectrum and chromophore yield.

    Downstream process integration

    • Added during early-stage chromophore assembly prior to diazotization or coupling reactions; later processing steps often include sulfonation and purification for increased color fastness.

    Final product types

    • High-performance azo dyes for technical textiles
    • Specialty pigments for automotive coatings
    • Advanced colorants for optoelectronic displays

    4. Advanced Material Synthesis for Liquid Crystal Intermediates

    Research-driven firms in the specialty materials sector employ this compound as a foundation for synthesizing mesogenic cores needed in advanced liquid crystal display (LCD) formulations. The specific substitution pattern directly influences the alignment and birefringence properties of intermediate compounds, helping downstream manufacturers achieve precise electro-optic characteristics. Batch quality and residue limits follow strict standards due to the high-sensitivity end uses.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for electronics applications)
    • ISO 14001 (environmental management systems for specialty chemicals)
    • Japan Industrial Standards (JIS) for liquid crystal raw materials
    • IEC 62474 (declaration of materials in electronic components)

    Typical usage ratio

    • 0.1–0.6 molar ratio, set in relation to core-forming reactants; exact dose chosen based on alignment requirements and device specification targets for LCD panel manufacturers.

    Downstream process integration

    • Introduced during the key intermediate assembly stages, particularly in the synthesis of biphenyl or cyanobiphenyl cores that define final mesogenic compound function; subsequent stages involve esterification or etherification.

    Final product types

    • Liquid crystal intermediates for high-resolution display panels
    • Performance-tuned mesogens for scientific instrumentation
    • Specialty fluidic materials for next-generation optical devices
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