N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative
N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative
CAS: 73772-48-2
Molecular Formula: C16H35N3O
N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative - Names and Identifiers
| Name | N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative |
| Synonyms | N,N-bis(2-aminoethyl)dodecanamide N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative |
| CAS | 73772-48-2 |
| EINECS | 277-602-7 |
N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative - Physico-chemical Properties
| Molecular Formula | C16H35N3O |
| Molar Mass | 285.4686 |
N-(2-aminoethyl)lauramide, N-(2-aminoethyl) derivative - Introduction
N-(2-aminoethyl) lauramide is an organic compound commonly abbreviated as AEL. Its chemical structure contains an amino group and an ethyl group. According to nomenclature, it is an N-(2-aminoethyl) substituted derivative of lauramide.
Regarding the properties of N-(2-aminoethyl) lauramide, it is a colorless to light yellow liquid with strong amine properties. It can be neutralized with weak acids and acidic substances in solution to form the corresponding salts. It is soluble in many organic solvents at room temperature, such as alcohols, ethers and ketones.
N-(2-aminoethyl) lauramide is widely used. It is commonly used as a buffer, enzyme catalyst and surfactant in biochemical, biochemical and pharmacological research. Because of its good surface activity and solubility, it is often used to prepare micelles, microemulsions and nanoparticles. In addition, N-(2-aminoethyl) lauramide is also useful in the preparation of pharmaceuticals, cosmetics, and personal care products, among others.
The method for preparing N-(2-aminoethyl) lauramide is relatively simple. One common method is to react lauric acid with 2-aminoethylamine under basic conditions to form N-(2-aminoethyl) lauramide. This reaction is carried out at room temperature, and commonly used bases are sodium hydroxide and potassium hydroxide.
For safety information, N-(2-aminoethyl) lauramide is a chemical and should be used with caution. It may decompose at high temperatures and produce harmful substances. During the operation, contact with skin, eyes and mucous membranes should be avoided to avoid irritation and damage. If ingested or inhaled, seek medical attention immediately. Pay attention to personal protective measures when using, such as wearing chemical protective gloves, goggles and protective clothing. During storage and transportation, avoid contact with strong oxidants and acidic substances to avoid dangerous reactions.
Regarding the properties of N-(2-aminoethyl) lauramide, it is a colorless to light yellow liquid with strong amine properties. It can be neutralized with weak acids and acidic substances in solution to form the corresponding salts. It is soluble in many organic solvents at room temperature, such as alcohols, ethers and ketones.
N-(2-aminoethyl) lauramide is widely used. It is commonly used as a buffer, enzyme catalyst and surfactant in biochemical, biochemical and pharmacological research. Because of its good surface activity and solubility, it is often used to prepare micelles, microemulsions and nanoparticles. In addition, N-(2-aminoethyl) lauramide is also useful in the preparation of pharmaceuticals, cosmetics, and personal care products, among others.
The method for preparing N-(2-aminoethyl) lauramide is relatively simple. One common method is to react lauric acid with 2-aminoethylamine under basic conditions to form N-(2-aminoethyl) lauramide. This reaction is carried out at room temperature, and commonly used bases are sodium hydroxide and potassium hydroxide.
For safety information, N-(2-aminoethyl) lauramide is a chemical and should be used with caution. It may decompose at high temperatures and produce harmful substances. During the operation, contact with skin, eyes and mucous membranes should be avoided to avoid irritation and damage. If ingested or inhaled, seek medical attention immediately. Pay attention to personal protective measures when using, such as wearing chemical protective gloves, goggles and protective clothing. During storage and transportation, avoid contact with strong oxidants and acidic substances to avoid dangerous reactions.
Last Update：2024-04-09 21:54:55
