Name | (4-tert-butylphenyl)methanamine |
Synonyms | AKOS 216-20 RARECHEM AL BW 0711 P-T-BUTYLBENZYLAMINE 4-(T-BUTYL)BENZYLAMINE 4-(t-Butyl)benzylamine 4-Tert-Butyl-Benzylamin 4-tort Butylbonzylamine 4-TERT-BUTYLBENZYLAMINE 4-tert-Butylbenzylamine 4-tert Butylbonzylamine 4-tert.butylbenzylamine 4-tert-Butyl-benzylamine 4-Tert-Butyl Benzylamine 4-TERT-BUTYLBENZYLAMINE HCL (4-tert-butylphenyl)methanamine 1-(4-tert-butylphenyl)methanamine |
CAS | 39895-55-1 |
EINECS | 254-681-6 |
InChI | InChI=1/C11H17N/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-7H,8,12H2,1-3H3 |
Molecular Formula | C11H17N |
Molar Mass | 163.26 |
Density | 0.927g/mLat 25°C(lit.) |
Boling Point | 235-236°C(lit.) |
Flash Point | 225°F |
Water Solubility | Not miscible or difficult to mix with water. |
Vapor Presure | 0.036mmHg at 25°C |
Appearance | Liquid |
Specific Gravity | 0.93 |
Color | Clear pale yellow |
BRN | 2961797 |
pKa | 9.24±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
Sensitive | Air Sensitive |
Refractive Index | 1.52-1.522 |
MDL | MFCD00040754 |
Physical and Chemical Properties | Density: 0.93 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36 - Irritating to the eyes |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S24/25 - Avoid contact with skin and eyes. |
UN IDs | 2735 |
WGK Germany | 3 |
HS Code | 29214990 |
Hazard Note | Irritant |
Hazard Class | 8 |
Packing Group | III |
Uses | 4-tert-butylbenzylamine is an effective compound for preparing imines by aerobic photocatalytic oxidation of aniline under titanium oxide catalysis. 4-tert-butylbenzylamine is a useful compound for preparing imines by aerobic photocatalytic oxidation of benzylamine catalyzed by TiO2. p-tert-butylaniline is an intermediate of the acaricide pyridoxamine. Used as pesticide intermediate |
production method | p-tert-butylbenzylamine is reacted with urotropine by tert-butylbenzyl chloride, ethanol or butanol is used as solvent, 30-35 ℃ is reacted for 4h, hydrochloric acid is added, then 45-50 ℃ is reacted for 2h, cooled to room temperature, ammonium chloride is filtered, desolated, and alkali is added to obtain the product. It can also be prepared by reducing p-tert-butylbenzonitrile with hydrogen or pressing p-tert-butylbenzaldehyde with ammonia and then reducing with hydrogen. |