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2-Bromobenzaldehyde

    • Product Name 2-Bromobenzaldehyde
    • Alias o-Bromobenzaldehyde
    • Einecs 209-999-4
    • 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

    603545

    Chemicalname 2-Bromobenzaldehyde
    Casnumber o-Bromobenzaldehyde
    Molecularformula C7H5BrO
    Molecularweight 185.02 g/mol
    Appearance Colorless to pale yellow liquid or solid
    Meltingpoint 29-32 °C
    Boilingpoint 238-239 °C
    Density 1.63 g/cm³
    Refractiveindex 1.627
    Flashpoint 104 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=CC(=C1Br)C=O
    Inchi InChI=1S/C7H5BrO/c8-7-3-1-2-6(4-7)5-9/h1-5H

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

    Packing & Storage
    Packing A 100g amber glass bottle labeled “2-Bromobenzaldehyde,” features hazard symbols, CAS number, lot number, and tightly sealed cap.
    Shipping 2-Bromobenzaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package should be clearly labeled with hazard information, and handled in accordance with applicable regulations for hazardous chemicals. Transport is typically via ground or air by certified carriers, ensuring compliance with safety and environmental guidelines.
    Storage 2-Bromobenzaldehyde should be stored in a tightly closed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area, preferably in a designated chemical storage cabinet. Avoid contact with oxidizing agents and moisture. Label containers clearly and follow all relevant safety protocols for handling hazardous organic chemicals.
    Application of 2-Bromobenzaldehyde

    Applications of 2-Bromobenzaldehyde in Industrial Manufacturing

    As a dedicated producer of 2-Bromobenzaldehyde, we supply this crucial intermediate to multiple sectors requiring reliable aromatic building blocks with strong reactivity. Below, we outline established downstream application scenarios, emphasizing differentiated industry compliance, formulation practices, integration in production, and real end products.

    1. Synthesis of Pharmaceutical Intermediates: Active Pharmaceutical Ingredient (API) Building Blocks

    Pharmaceutical manufacturers employ this compound as a key benzaldehyde unit for constructing specialty intermediates integral to antihypertensive agents, antifungal medications, and certain psychoactive drugs. Our quality systems align formulation supply to stringent drug precursor standards, supporting scalable batch processes with rigorous documentation. The aromatic bromine on the molecule facilitates further transformations by nucleophilic substitution or carbonyl condensation, paving the way for tailored molecular entities with strict impurity control.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monograph specifications for raw materials
    • EU EudraLex Vol. 4 GMP standards
    • 21 CFR Part 211 (US FDA current Good Manufacturing Practice)

    Typical usage ratio

    • 0.2%–2.5% w/w of final API batch, with dosage adjusted based on specific target molecule requirements; stoichiometry determined by route of synthesis and intended functionalization.

    Downstream process integration

    • Introduced during early or intermediate steps in multi-stage synthesis; commonly subjected to Grignard reactions, Wittig reactions, or reductive aminations within closed reactor systems, followed by phase separation and purification operations.

    Final product types

    • Cardiovascular drug APIs (e.g., beta-blockers precursors)
    • Triazole-based antifungal intermediates
    • Precursors for central nervous system agents
    • Benzimidazole or benzoxazole scaffold intermediates

    2. Agrochemical Intermediate Production: Herbicide and Fungicide Synthesis

    Manufacturers in the crop protection sector utilize 2-Bromobenzaldehyde for its reactivity within the synthesis of novel herbicidal and fungicidal compounds, particularly those containing benzylidene or heterocyclic moieties vital for binding activity. Our material integrates directly into pilot and industrial-scale processes, matched to international chemical safety protocols for agrograde supply while addressing consistent halogen content and low residual metals.

    Industry compliance standards

    • FAO/WHO Specification and Evaluations for Agricultural Pesticides (JMPS)
    • ISO 9001:2015 Quality Management System for agrochemical synthesis plants
    • EU Regulation (EC) No 1107/2009 for plant protection product approval
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance for intermediates

    Typical usage ratio

    • 1.0%–5.0% by mass in synthesis batches, depending on the targeted crop-protection molecule and reaction efficiency; batches tailored to annual demand and regulatory dossiers.

    Downstream process integration

    • Deployed as a reagent in condensation reactions, particularly for synthesizing aromatic heterocycles or substituted benzylidene derivatives; processed with base- or acid-catalyzed conditions, followed by refining and crystallization according to agrochemical impurity profiles.

    Final product types

    • Precursor to triazole-based fungicides
    • Intermediate for phenylhydrazone type herbicides
    • Sub-unit in selective weed killer synthetic chains
    • Building block for heterocyclic insecticides

    3. Fine Chemical Synthesis: Advanced Dye and Pigment Manufacturing

    Developers of specialty dyes and pigments integrate this aromatic aldehyde for introducing brominated functional groups that enable unique color properties and solubility modifications. Its reactivity supports formation of complex Schiff bases and extended conjugated systems, which are fundamental to producing intense and durable colorants for plastics, inks, and fibers. We coordinate product traceability for fine chemical usages, catering to labs and scaling industrial pigment lines.

    Industry compliance standards

    • EN ISO 9001 for quality management in colorant production
    • Oeko-Tex Standard 100 (for textiles and dyes used in fabrics)
    • GHS (Globally Harmonized System of Classification and Labelling of Chemicals) for material safety
    • EU REACH pre-registration for dye intermediates

    Typical usage ratio

    • Ranging from 0.5%–3.0% of total pigment synthesis formulation; selected according to chromophore design, shade strength, and process yield.

    Downstream process integration

    • Applied in initial steps of Schiff base formation, bromination, or as electrophilic partner in Suzuki or Heck couplings within dye molecule construction; undergoes post-reaction purification (recrystallization or column separation) for final pigment isolation.

    Final product types

    • Brominated azo dyes for synthetic fibers
    • Intermediate for fluorescent pigments
    • Semi-permanent textile dyestuffs
    • Industrial plastic and printing ink colorants

    4. Fragrance and Aroma Chemical Manufacturing: Synthesis of Specialty Aromatic Compounds

    Producers of fine fragrance ingredients and aroma intermediates apply this compound for its benzaldehyde backbone and bromination, serving both as a starting material in musk fragrances and as a precursor to unique aromatic aldehydes with high olfactory impact. Our controlled production meets the exacting purity and trace organics criteria required for cosmetic and perfumery applications, while providing batch-to-batch traceability for regulatory submissions.

    Industry compliance standards

    • IFRA International Fragrance Association Standards
    • ISO 9001:2015 for fragrance ingredient supply
    • Cosmetic Regulation (EC) No 1223/2009 for ingredient purity and labeling
    • Global Product Authentication and Traceability protocols

    Typical usage ratio

    • 0.1%–0.6% of total aroma chemical batch; carefully adjusted based on desired fragrance note synthesis and conversion rates in multi-step reactions.

    Downstream process integration

    • Introduced at the aldehyde transformation stage, supporting formation of macrocyclic musk intermediates or brominated aromatic aldehydes; subjected to catalytic hydrogenation, reductive amination, or complexation reactions, followed by distillation and GC/FID quality testing.

    Final product types

    • Musk fragrance intermediates
    • Brominated benzaldehyde-based aroma chemicals
    • Blending components for high-end perfumes
    • Specialty aldehyde blends for personal care products

    5. Organic Laboratory Reagents: Research and Development Applications

    Chemical research institutions and industrial R&D centers regularly utilize this material as a specialized reagent for mechanism exploration, library synthesis, and reference standard preparation. The well-documented reactivity with nucleophiles and organometallic agents supports rapid route screening across pharmaceutical, materials, and process chemistry programs. We consistently supply analytical-grade batches for protocol development, streamlining downstream analysis and product validation.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Quality Management
    • GLP (OECD Good Laboratory Practice) for chemical research
    • GHS-compliant labeling and documentation
    • Certified Reference Material (CRM) standards as applicable

    Typical usage ratio

    • Variable: 5–500 mg per reaction setup or 0.05–1.0 mmol, depending on scale and purpose; experimental planning determines dosage according to substrate scope.

    Downstream process integration

    • Dissolved or suspended in appropriate solvents, introduced for stepwise transformation, tandem reactions, or kinetic profiling; samples undergo direct spectroscopic or chromatographic analysis post-reaction.

    Final product types

    • Reference standards for analytical labs
    • Novel molecular libraries for drug research
    • R&D process investigation samples
    • Synthetic intermediates for advanced material studies
    Free Quote

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