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| | 4-tert-Butylaniline Basic information |
| | 4-tert-Butylaniline Chemical Properties |
| Melting point | 15-16 °C (lit.) | | Boiling point | 90-93 °C/3 mmHg (lit.) | | density | 0.937 g/mL at 25 °C (lit.) | | vapor pressure | 5.34-5.77Pa at 25℃ | | refractive index | n20/D 1.538(lit.) | | Fp | 215 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | Liquid | | pka | pK1: 3.78(+1) (25°C) | | Specific Gravity | 0.937 | | color | Clear orange-red to brownish | | Water Solubility | Insoluble in water. | | Sensitive | Light Sensitive | | BRN | 2205786 | | LogP | 2.7-2.99 | | CAS DataBase Reference | 769-92-6(CAS DataBase Reference) | | NIST Chemistry Reference | 4-Tert-butylbenzeneamine(769-92-6) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 2 | | Hazard Note | Irritant | | HS Code | 29214980 |
| | 4-tert-Butylaniline Usage And Synthesis |
| Chemical Properties | clear orange-red to brownish liquid | | Uses | 4-tert-Butylaniline reacts with formic acid to produce formic acid-(4-tert-butyl-anilide). This reaction could happen in the presence of the solvent of toluene in the condition of heating. 4-tert-Butylaniline is used in the synthesis of 4-tert-Butyl-4?,4?-dinitrotriphenylamine, new triphenylamine-containing diamine monomer and 2-oxopyrimido[4,5-d]pyrimidin-5(6H)-one. | | General Description | Schiff base formation reaction between 4-tert-butylaniline and 4-tert-butylbenzaldehyde in ethanol has been carried out using the matrix-assisted laser desorption ionization-chip system. |
| | 4-tert-Butylaniline Preparation Products And Raw materials |
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