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HS Code |
437089 |
| Product Name | 2-Bromooctanoyl Bromide |
| Cas Number | 32188-65-9 |
| Molecular Formula | C8H14Br2O |
| Molecular Weight | 302.01 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.68 g/cm3 (approximate) |
| Refractive Index | n20/D 1.517 (lit.) |
| Purity | Typically ≥ 95% |
| Solubility | Reacts with water; soluble in organic solvents like dichloromethane |
| Synonyms | 2-Bromooctanoyl bromide, α-Bromooctanoyl bromide |
| Storage Conditions | Store under inert atmosphere at 2-8°C |
| Hazard Statements | Corrosive, causes severe skin burns and eye damage |
As an accredited 2-Bromooctanoyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Bromooctanoyl Bromide is supplied in a 25g amber glass bottle, securely sealed with a PTFE-lined cap for safe storage. |
| Shipping | 2-Bromooctanoyl Bromide is shipped in tightly sealed, corrosion-resistant containers to prevent moisture and air exposure. It is handled as a hazardous material, following all safety and regulatory guidelines. During transit, the chemical is kept upright, protected from sunlight, and stored at controlled temperatures to ensure stability and minimize risks. |
| Storage | 2-Bromooctanoyl Bromide should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from moisture and incompatible substances such as strong bases, oxidizing agents, and water. It should be kept under an inert atmosphere, like nitrogen, to prevent hydrolysis. Protect from light and handle in a designated chemical fume hood. |
Applications of 2-Bromooctanoyl Bromide in Industrial ManufacturingAs a direct chemical raw material manufacturer, we provide 2-Bromooctanoyl Bromide to a range of specialized downstream sectors. Each industry uses this acyl bromide based on strict regulatory standards, precise formulation methods, and highly controlled process steps. Below we outline key application areas, including details on compliance, dosage, integration into existing production lines, and resulting downstream products. 1. Pharmaceutical Intermediate for Synthesis of Antiviral AgentsPharmaceutical formulators employ 2-Bromooctanoyl Bromide as a building block for specialized antiviral compound synthesis, especially in research and commercial scale-up for novel nucleoside analogues. Our customers integrate this material into alkylation steps that require precise reaction conditions and high purity input. Its brominated chain facilitates selective ring closures during active pharmaceutical ingredient (API) formation. Industry compliance standards
Typical usage ratio
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2. Agrochemical Active Ingredient Synthesis – Herbicide IntermediatesManufacturers in the crop protection sector utilize 2-Bromooctanoyl Bromide to construct selective alkyl chain-bearing intermediates for modern herbicide actives. Its use centers on acylation reactions in controlled batch reactors, with downstream benefits for herbicide molecular diversity and soil persistence profiles. Strict traceability and impurity control support global regulatory acceptance. Industry compliance standards
Typical usage ratio
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3. Specialty Chemical Manufacturing – Synthesis of Fatty Acyl DerivativesProducers of bespoke specialty chemicals adopt 2-Bromooctanoyl Bromide for the synthesis of functionalized fatty acyl derivatives used in high-performance coatings and advanced surfactants. In this domain, accuracy in dosing and rigorous monitoring of reaction progress are vital, as the presence of bromine offers reactivity control during further functionalization steps such as esterification or amidation for tailor-made surface properties. Industry compliance standards
Typical usage ratio
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4. Fine Chemical Synthesis – Fluorinated Compound IntermediatesFine chemical companies value 2-Bromooctanoyl Bromide as an acylating agent for high-value intermediates in the production of fluorinated compounds used in electronics, analytical standards, and performance fluids. Its controlled reactivity with nucleophilic bases enables construction of stable, functionalized molecules with tight batch reproducibility. Highly qualified operators manage each critical point in the process to ensure trace impurity control. Industry compliance standards
Typical usage ratio
Downstream process integration
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