PIPERIDINIUM ACETATE
piperidinium acetate
CAS: 4540-33-4
Molecular Formula: C7H15NO2
PIPERIDINIUM ACETATE - Names and Identifiers
| Name | piperidinium acetate |
| Synonyms | piperidin-1-iuM piperidinium acetate Piperidinium acetate PIPERIDINIUM ACETATE piperidiniumacetate(ep) Piperidin-1-iuM acetate |
| CAS | 4540-33-4 |
| EINECS | 224-890-7 |
| InChI | InChI=1/C5H11N.C2H4O2/c1-2-4-6-5-3-1;1-2(3)4/h6H,1-5H2;1H3,(H,3,4) |
PIPERIDINIUM ACETATE - Physico-chemical Properties
| Molecular Formula | C7H15NO2 |
| Molar Mass | 145.2 |
| Density | 0.9366 g/cm3 |
| Melting Point | 106 °C |
| Boling Point | 96-98 °C(Press: 9 Torr) |
| Flash Point | 4.4°C |
| Vapor Presure | 28.3mmHg at 25°C |
| Physical and Chemical Properties | White solid |
PIPERIDINIUM ACETATE - Risk and Safety
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
PIPERIDINIUM ACETATE - Introduction
piperidinium acetate, also known as piperidine acetic acid, is an organic compound with the chemical formula C6H11NO2. It is a colorless or pale yellow solid with a special ammonia aroma. The following is a description of the nature, use, preparation and safety information of piperidinium acetate:
Nature:
- piperidinium acetate are solids that are soluble in water and certain organic solvents.
-It is a basic compound that can react with acid to form the corresponding salt.
-piperidinium acetate at low temperature will crystallize out anhydrate, which has a lower melting point.
Use:
- piperidinium acetate are often used as basic catalysts in organic synthesis, such as some acylation reactions and esterification reactions.
-It can also be used to prepare organic compounds such as pesticides and medicines.
Preparation Method:
- piperidinium acetate can be prepared by reacting piperidine with acetic acid.
-The reaction is usually carried out in an alcohol solvent. First, acetic acid is reacted with a base to generate the corresponding acetate salt, and then reacted with piperidine to obtain the piperidinium acetate.
-Finally, the piperidinium acetate is precipitated by crystallization or evaporation of the solvent.
Safety Information:
- piperidinium acetate have a certain irritation, contact with the skin or inhalation may cause irritation or allergic reactions.
-Wear appropriate personal protective equipment, such as lab gloves and protective glasses, during operation or contact.
-When storing and handling piperidinium acetate, take appropriate safety measures and avoid contact with heat sources and oxidants.
Nature:
- piperidinium acetate are solids that are soluble in water and certain organic solvents.
-It is a basic compound that can react with acid to form the corresponding salt.
-piperidinium acetate at low temperature will crystallize out anhydrate, which has a lower melting point.
Use:
- piperidinium acetate are often used as basic catalysts in organic synthesis, such as some acylation reactions and esterification reactions.
-It can also be used to prepare organic compounds such as pesticides and medicines.
Preparation Method:
- piperidinium acetate can be prepared by reacting piperidine with acetic acid.
-The reaction is usually carried out in an alcohol solvent. First, acetic acid is reacted with a base to generate the corresponding acetate salt, and then reacted with piperidine to obtain the piperidinium acetate.
-Finally, the piperidinium acetate is precipitated by crystallization or evaporation of the solvent.
Safety Information:
- piperidinium acetate have a certain irritation, contact with the skin or inhalation may cause irritation or allergic reactions.
-Wear appropriate personal protective equipment, such as lab gloves and protective glasses, during operation or contact.
-When storing and handling piperidinium acetate, take appropriate safety measures and avoid contact with heat sources and oxidants.
Last Update：2024-04-09 21:00:56
