Benzenamine, 3-(1-methylpropoxy)-
3-(sec-Butoxy)aniline
CAS: 65382-94-7
Molecular Formula: C10H15NO
Benzenamine, 3-(1-methylpropoxy)- - Names and Identifiers
| Name | 3-(sec-Butoxy)aniline |
| Synonyms | 3-(sec-Butoxy)aniline 3-(SEC-BUTOXY)ANILINE 3-(sec-butoxy)phenylamine Benzenamine, 3-(1-methylpropoxy)- |
| CAS | 65382-94-7 |
Benzenamine, 3-(1-methylpropoxy)- - Physico-chemical Properties
| Molecular Formula | C10H15NO |
| Molar Mass | 165.23 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD09055135 |
Benzenamine, 3-(1-methylpropoxy)- - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
Benzenamine, 3-(1-methylpropoxy)- - Introduction
3-(sec-Butoxy)aniline(3-(n-butoxy) aniline) is an organic compound with the formula C10H15NO. It is a colorless to pale yellow liquid with a peculiar odor.
3-(sec-Butoxy)aniline are mainly used as intermediates in organic synthesis reactions. It can be used to synthesize different compounds, such as dyes, drugs and pesticides. It can also be used for reducing agents, catalysts and ligands in organic synthesis reactions.
There are many methods for preparing 3-(sec-Butoxy)aniline, and the commonly used method is obtained by the reaction of aniline and n-butanol. The reaction conditions are generally high temperature and high pressure, using acidic or basic catalysts.
For safety information, 3-(sec-Butoxy)aniline is irritating and corrosive to eyes, skin and respiratory tract. Care should be taken to avoid inhaling its vapors or splashing onto eyes, skin and clothing. Use appropriate protective equipment such as gloves, goggles and protective clothing. Avoid contact with oxidants and strong acids. Good ventilation should be maintained during storage and use. If exposed or inhaled, seek medical attention immediately. Observe relevant safety operation regulations.
3-(sec-Butoxy)aniline are mainly used as intermediates in organic synthesis reactions. It can be used to synthesize different compounds, such as dyes, drugs and pesticides. It can also be used for reducing agents, catalysts and ligands in organic synthesis reactions.
There are many methods for preparing 3-(sec-Butoxy)aniline, and the commonly used method is obtained by the reaction of aniline and n-butanol. The reaction conditions are generally high temperature and high pressure, using acidic or basic catalysts.
For safety information, 3-(sec-Butoxy)aniline is irritating and corrosive to eyes, skin and respiratory tract. Care should be taken to avoid inhaling its vapors or splashing onto eyes, skin and clothing. Use appropriate protective equipment such as gloves, goggles and protective clothing. Avoid contact with oxidants and strong acids. Good ventilation should be maintained during storage and use. If exposed or inhaled, seek medical attention immediately. Observe relevant safety operation regulations.
Last Update：2024-04-09 20:02:46
