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HS Code |
937985 |
| Productname | 3-Aminocarbonylphenylboronic Acid |
| Casnumber | 511295-38-6 |
| Molecularformula | C7H8BNO3 |
| Molecularweight | 164.96 g/mol |
| Appearance | White to off-white powder |
| Meltingpoint | 210-215°C (decomposition) |
| Purity | ≥98% |
| Solubility | Slightly soluble in water, soluble in DMSO and methanol |
| Storagetemperature | 2-8°C |
| Smiles | B(C1=CC(=CC=C1)C(=O)N)(O)O |
As an accredited 3-Aminocarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5g amber glass bottle labeled "3-Aminocarbonylphenylboronic Acid," with hazard symbols, lot number, and storage instructions on the label. |
| Shipping | 3-Aminocarbonylphenylboronic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. The chemical is handled as hazardous material, packed according to safety regulations, and accompanied by appropriate labeling and documentation. Shipping occurs under controlled conditions, ensuring compliance with relevant guidelines for safe transport and storage. |
| Storage | 3-Aminocarbonylphenylboronic acid should be stored in a tightly sealed container, protected from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Store at room temperature away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and follow standard laboratory chemical storage practices to maintain its stability and prevent degradation or contamination. |
Applications of 3-Aminocarbonylphenylboronic Acid in Industrial Manufacturing3-Aminocarbonylphenylboronic acid serves as a specialized synthetic intermediate in several industrial sectors. Our manufacturing focus ensures traceable quality and consistency, supporting complex performance and regulatory criteria across each targeted downstream application. Below, we outline its established industrial uses—detailing compliance requirements, dosing guidelines, process placement, and real commercial product outputs for each scenario. 1. API Synthesis in Targeted Antineoplastic AgentsPharmaceutical companies rely on this boronic acid derivative during multistep synthesis routes for boronate-containing anticancer APIs, especially in processes requiring Suzuki-Miyaura coupling. Its specific structure supports site-selective functionalization, allowing chemists to construct biaryl motifs found in emerging kinase inhibitors. We supply material meeting purity specifications suitable for regulated drug substance manufacturing, with full batch traceability and dedicated quality documentation for customer DMF integration. Industry compliance standards
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2. Fluorescent Glucose Sensor ManufacturingThis compound provides the essential boronic acid functionality for covalent immobilization on sensor matrices, used in point-of-care glucose monitoring devices. Its precise amide and amine groups enhance conjugation and stability during surface modification steps. Industrial users integrate it during molecular imprinting of polymer membranes or in direct functionalization of silica-based sensor chips, forming the core recognition element that binds diols in analytical chemistry applications. Industry compliance standards
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3. Fine Chemical Synthesis of Boron-Containing Agrochemical IntermediatesMajor agrochemical manufacturers use this intermediate for constructing boronated heterocycles and phenyl derivatives with improved bioactivity and environmental persistence. Its optimal reactivity profile ensures high-yield transformations under palladium-catalyzed conditions, enabling efficient production of novel fungicide and insecticide intermediates. Quality assurance focuses on minimization of trace heavy metals and consistent physical properties to meet downstream formulation demands. Industry compliance standards
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4. Functional Polymer Modification for Electronic MaterialsIn the electronics sector, 3-aminocarbonylphenylboronic acid is used as a functional monomer for introducing boronic acid groups onto aromatic polymer chains, enhancing their performance in organic semiconductors, OLEDs, and printable circuits. Process engineers value its dual reactivity, facilitating direct incorporation via copolymerization or post-polymerization grafting, delivering improved thermal stability and charge-transport characteristics in next-generation electronic components. Industry compliance standards
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