N-benzyl-N-isopropylpropan-2-amine
$250.00
CAS No.: 34636-09-4
Catalog No.: 195051
Purity: 95%
MF: C13H21N
MW: 191.318
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N(C(C)C)C(C)C
Catalog No.: 195051
Purity: 95%
MF: C13H21N
MW: 191.318
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N(C(C)C)C(C)C
N-benzyl-N-isopropylpropan-2-amine; CAS No.: 34636-09-4; N-benzyl-N-isopropylpropan-2-amine. PROPERTIES: N-benzyl-N-isopropylpropan-2-amine appears as a colorless to pale yellow liquid with a slight amine odor. Its molecular formula is C12H19N, corresponding to a molecular weight of approximately 177.29 g/mol. The compound exhibits a boiling point around 220-225 C at 760 mmHg and a density of about 0.88 g/cm? at 25 C. It demonstrates moderate solubility in common organic solvents such as toluene, hexane, and diethyl ether but is sparingly soluble in water. The substance is sensitive to oxidation and may form explosive peroxides upon prolonged storage. Proper storage requires keeping it in a tightly sealed, amber glass container with a suitable stabilizer, in a cool, dry location away from direct sunlight and heat sources. The temperature should be maintained below 10 C if possible. Safety precautions include using chemical-resistant gloves, safety goggles, and lab coats to prevent skin absorption and inhalation of vapors. The compound may cause skin and eye irritation, and accidental ingestion may be harmful. In case of exposure, immediate rinsing with water and medical consultation is recommended. APPLICATIONS: N-benzyl-N-isopropylpropan-2-amine functions as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the preparation of certain antidepressants and antipsychotics, through its ability to participate in nucleophilic aromatic substitution reactions and cross-coupling processes (Journal of Medicinal Chemistry). In chemical analysis, N-benzyl-N-isopropylpropan-2-amine serves as a chelating agent for metal ions, forming stable complexes with transition metals for separation and quantification purposes (Analytical Chemistry). Additionally, it finds application in the preparation of corrosion inhibitors for metal surfaces, where its amine group adsorbs onto metal substrates to prevent oxidation and degradation (Corrosion Science). The compound is also employed in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science).
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