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HS Code |
955033 |
| Chemical Name | 2-Bromo-2'-Hydroxyacetophenone |
| Molecular Formula | C8H7BrO2 |
| Molecular Weight | 215.05 g/mol |
| Cas Number | 24715-06-2 |
| Appearance | White to off-white solid |
| Melting Point | 70-74 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC(=O)C1=CC=CC=C1OBr |
| Iupac Name | 1-(2-Bromo-2-hydroxyphenyl)ethan-1-one |
| Storage Conditions | Store at 2-8°C, dry, well-ventilated area |
As an accredited 2-Bromo-2'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-2'-Hydroxyacetophenone, sealed with a screw cap and labeled with hazard warnings. |
| Shipping | 2-Bromo-2'-Hydroxyacetophenone is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous chemical, following DOT, IATA, or IMDG regulations. Packaging is in accordance with safety standards, with clear hazard labeling. Temperature and ventilation controls are maintained to avoid decomposition or hazardous reactions during transit. |
| Storage | Store 2-Bromo-2'-Hydroxyacetophenone 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 light and moisture. Clearly label the container and ensure access is limited to trained personnel. Follow all applicable safety and handling guidelines for hazardous chemicals. |
Applications of 2-Bromo-2'-Hydroxyacetophenone in Industrial Manufacturing2-Bromo-2'-Hydroxyacetophenone is a specialized chemical intermediate widely adopted in targeted segments of pharmaceuticals, fine chemicals, and advanced material manufacturing. As the original producer, we prioritize precise integration of this material in highly controlled production chains, ensuring each usage matches critical regulatory and performance demands. Below are core application scenarios in which this substance contributes essential reactivity and structural features for advanced derivatives. 1. Pharmaceutical Intermediates for API SynthesisThis compound serves as a crucial building block in the synthesis of pharmaceutical active ingredients, especially for selective kinase inhibitors and related heterocyclic drug molecules. Manufacturers utilize its bromine and hydroxy groups to achieve regioselective modifications, allowing reliable introduction of targeted moieties in multi-step flow or batch synthesis routes. Product consistency and traceability remain focal points throughout all stages of handling and formulation, as end use connects directly to regulated finished pharmaceuticals. Industry compliance standards
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2. Light Stabilizer Intermediate for UV AbsorbersChemical manufacturers incorporate this raw material in the targeted synthesis of benzotriazole and salicylate-based UV absorbers, used extensively in plastics, coatings, and inks requiring protection against photodegradation. The hydroxy and bromo functionalities enable efficient coupling with triazoles and other aromatic platforms, conferring strong UV-shielding properties after ring closure and downstream derivatization. Industry compliance standards
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3. Fine Chemical Intermediate for Agrochemical SynthesisIn crop protection chemical development, this material plays a role as a precursor in the elaboration of benzoxazole and related heterocyclic cores found in specific fungicidal and herbicidal actives. The brominated acetophenone structure is exploited for regioselective ring closure and further halide displacement reactions, enabling scalable, cost-effective introduction of essential biological motifs in protected environments. Industry compliance standards
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4. Component for High-Performance PhotoinitiatorsProducers of UV-curable resins and inks employ this compound as a structural intermediate to introduce advanced benzoyl moieties in specialty photoinitiators. The material’s functional group profile facilitates controlled acylation or etherification, yielding modified photoinitiators with precise activation wavelengths and surface compatibility, supporting fast polymerization in 3D printing and industrial coatings. Industry compliance standards
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