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HS Code |
455383 |
| Chemical Name | Tert-Butyl 3-Aminobenzoate |
| Cas Number | 136153-82-1 |
| Molecular Formula | C11H15NO2 |
| Molecular Weight | 193.24 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 57-61°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Purity | Typically ≥98% |
| Smiles | CC(C)(C)OC(=O)C1=CC(=CC=C1)N |
As an accredited Tert-Butyl 3-Aminobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Tert-Butyl 3-Aminobenzoate, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and detailed labeling. |
| Shipping | Tert-Butyl 3-Aminobenzoate should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Use appropriate packaging to prevent leaks or spills. Follow all local, national, and international regulations for the transportation of chemicals, ensuring clear labeling and documentation for safe and compliant delivery. |
| Storage | Tert-Butyl 3-Aminobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and sources of ignition. Protect from light and incompatible materials such as strong acids and oxidizing agents. Ensure proper labeling and keep the storage area accessible only to trained personnel. Use appropriate personal protective equipment when handling. |
Applications of Tert-Butyl 3-Aminobenzoate in Industrial ManufacturingAs a specialist manufacturer of Tert-Butyl 3-Aminobenzoate, we support a select group of industries by providing this key intermediate for downstream synthesis. The following application scenarios reflect established, large-volume sectors where our material enters complex production lines and meets regulatory and quality benchmarks central to commercial operations. 1. Pharmaceutical Active Pharmaceutical Ingredient IntermediatesAPI manufacturers rely on our material as a structurally significant intermediate for the synthesis of various small-molecule drugs, particularly targeted therapeutics in anti-inflammatory and central nervous system categories. The stability conferred by the tert-butyl ester group and amine functionality assists in advanced side-chain constructions during multi-step syntheses, with the product often incorporated before a final deprotection or amidation stage. The choice of this intermediate is dictated by compendial requirements and established synthetic routes, necessitating strict quality assurance at each batch release. Industry compliance standards
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2. Organic Photoinitiator SynthesisChemical companies in the specialty materials sector utilize Tert-Butyl 3-Aminobenzoate to manufacture core fragments for photoinitiators deployed in inks, polymerizations, and UV-cured coatings. The material enters as a nucleophilic aromatic amine reactant that allows targeted diazotization or coupling to functionalize benzene rings for effective UV-light absorption. Producers demand this intermediate in high-purity, non-aqueous formats to ensure reaction efficiency and minimize downstream impurities. Industry compliance standards
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3. Agrochemical Synthesis of Herbicide IntermediatesMajor agrochemical enterprises source our product for integration into the synthesis of substituted benzoate herbicides and safeners. Its amine group facilitates specific acylation and ring substitution steps, essential for tailoring the mode-of-action profile of the resulting crop protection molecules. The purity and batch-to-batch consistency of our material underpin quality assurance in final actives destined for regional and international regulatory submissions. Industry compliance standards
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4. Specialty Polymer Modifier ManufacturingProducers of specialty polymers deploy this intermediate for constructing functionalized monomers that introduce amine-reactive sites, supporting the design of high-performance engineering plastics and electronic encapsulants. Its tert-butyl ester offers a removable protecting group during controlled radical or condensation polymerization, with subsequent post-polymerization deprotection enabling site-specific crosslinking or further derivatization. Industry compliance standards
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