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HS Code |
867549 |
| Iupac Name | 1-(2-hydroxy-5-nitrophenyl)ethan-1-one |
| Molecular Formula | C8H7NO4 |
| Molecular Weight | 181.15 g/mol |
| Cas Number | 2660-70-6 |
| Appearance | Yellow solid |
| Melting Point | 122-125°C |
| Solubility In Water | Slightly soluble |
| Smiles | CC(=O)C1=C(C=CC(=C1)N(=O)=O)O |
As an accredited 2'-Hydroxy-5'-Nitroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, tightly sealed with screw cap, labeled with chemical name, formula, hazard symbols, and manufacturer details. |
| Shipping | 2'-Hydroxy-5'-Nitroacetophenone is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be transported as a chemical substance under standard chemical shipping regulations, with appropriate labeling and documentation. Store in a cool, dry place, away from incompatible materials, and handle using suitable protective equipment during transit. |
| Storage | 2'-Hydroxy-5'-Nitroacetophenone should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Store at room temperature and avoid exposure to excessive heat. Properly label the storage area and follow all local regulatory guidelines for chemical storage. |
Applications of 2'-Hydroxy-5'-Nitroacetophenone in Industrial ManufacturingOur facility produces 2'-Hydroxy-5'-Nitroacetophenone to exacting quality standards, supporting key downstream industries where its functional properties contribute directly to advanced end formulations. This section details concrete industrial sectors where this specialty intermediate delivers precise value, addressing regulatory expectations, recommended formulation ranges, established integration methods, and the range of commercial end products our partners manufacture. 1. UV Stabilizer Intermediate Manufacturing for Polymer AdditivesMajor polymer additive producers utilize our product as a building block in the synthesis of benzophenone-based UV absorbers, which are critical in protecting plastics from discoloration and brittleness under prolonged sunlight exposure. The material enters the core condensation stage with specific dihydroxybenzene derivatives, providing the key nitro and hydroxy moieties essential for subsequent transformations under controlled hydrogenation and nucleophilic substitution sequences. Industry compliance standards
Typical usage ratio
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2. Pharmaceutical Intermediate in Antifungal Active Ingredient SynthesisIn the synthesis of specific antifungal agents, this raw material contributes to the production of heterocyclic compounds containing benzophenone backbone modifications. API manufacturers employ the compound during the early-stage diketone formation, setting the reactive framework that supports further amination, cyclization, and nitro group reduction steps necessary to achieve pharmacologically active structures. Industry compliance standards
Typical usage ratio
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3. Synthesis of High-Performance Pigment PrecursorsPigment manufacturers incorporate this chemical when producing azo and nitroaromatic pigment intermediates, valued for their intense yellow to orange chromaticity and strong lightfastness. The raw material participates in the diazotization or coupling reactions with anilines, where its functional groups ensure high reactivity and selectivity during pigment core construction. This drives the formation of high-purity intermediates suitable for advanced pigment dispersion. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Agrochemical Active Ingredient SynthesisOur manufacturing partners in the agrochemical sector use this compound for constructing select nitro- and hydroxy-containing heterocycles, which function as critical groups in the final formulation of herbicides and seed coatings. During the key condensation or substitution process, the chemical introduces necessary electronic properties to enhance binding and biological activity in soil or foliar application products. Industry compliance standards
Typical usage ratio
Downstream process integration
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