Description
2-(1,3-Dimethylbutyl)aniline (CAS No. 203448-76-4) is a high-purity aromatic amine compound with the molecular formula C12H19N. This specialized chemical, also known by its IUPAC name 2-(4-methylpentan-2-yl)aniline, features a unique branched alkyl substitution on the aniline ring, making it valuable for synthetic organic chemistry and material science applications. Our product is rigorously tested to ensure ≥98% purity (GC) and is supplied as a clear to pale-yellow liquid with minimal moisture content. Ideal for researchers developing advanced intermediates, ligands, or functionalized polymers, this compound is packaged under inert gas in amber glass vials to ensure stability. Available in quantities from 1g to 1kg, with custom bulk options upon request. SDS and analytical certificates (CoA, NMR, HPLC/GC-MS) are provided.
Properties
- CAS Number: 203448-76-4
- Complexity: 142
- IUPAC Name: 2-(1,3-dimethylbutyl)aniline
- InChI: InChI=1S/C12H19N/c1-9(2)8-10(3)11-6-4-5-7-12(11)13/h4-7,9-10H,8,13H2,1-3H3
- InChI Key: LPZZJKBLKQOBMZ-UHFFFAOYSA-N
- Exact Mass: 177.151749610
- Molecular Formula: C12H19N
- Molecular Weight: 177.29
- SMILES: CC(C)CC(C)C1=CC=CC=C1N
- Topological: 26
- Monoisotopic Mass: 177.151749610
- Synonyms: 203448-76-4, 2-(4-methylpentan-2-yl)aniline, 2-(1,3-dimethylbutyl)aniline, DTXSID601019696, DTXCID601477616, 700-095-5, 2-(1,3-Dimethylbutyl)benzenamine, Benzenamine, 2-(1,3-dimethylbutyl)-, 2-(1,3-dimethylbutyl)-Benzenamine, 2-(1,3-Dimethylbutyl)benzenamine; 2-(1,3-Dimethylbutyl)aniline; 2-(1,3-Dimethylbutyl)phenylamine; 2-(4-Methylpentan-2-yl)aniline, SCHEMBL708994, LPZZJKBLKQOBMZ-UHFFFAOYSA-N, 2-(1,3-dimethylbutyl)phenylamine, MFCD20690644, AKOS037650887, CS-15449, DS-022172, CS-0030818, NS00002819, C13510
Application
2-(1,3-Dimethylbutyl)aniline serves as a key intermediate in the synthesis of agrochemicals, pharmaceuticals, and specialty polymers. Its sterically hindered aniline structure is exploited in catalytic ligand design for asymmetric transformations. Researchers also utilize it to modify dye structures for enhanced photostability or as a building block in supramolecular chemistry. The compound’s lipophilic alkyl chain may improve bioavailability in drug development.
Safety and Hazards
GHS Hazard Statements
- H411 (100%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Precautionary Statements
- P273, P391, and P501
Hazard Classes and Categories
- Aquatic Chronic 2 (100%)
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