Other grades of this product :
| 2-Acetylaminoethanol Basic information | | Synthesis |
| Product Name: | 2-Acetylaminoethanol | | Synonyms: | 2-acetylamino-ethanol;Acetamide MEA;Acetamide MEA (1:1);Acetylcolamine;Lipamide MEAA;Mackamide AME-75, AME-100;n-(2-hydroxyethyl)-acetamid;N-(beta-Hydroxyethyl)acetamide | | CAS: | 142-26-7 | | MF: | C4H9NO2 | | MW: | 103.12 | | EINECS: | 205-530-8 | | Product Categories: | | Mol File: | 142-26-7.mol |
| 2-Acetylaminoethanol Chemical Properties |
| Melting point | 15.8 °C | | Boiling point | 151-155 °C/5 mmHg (lit.) | | density | 1.12 g/mL at 25 °C (lit.) | | vapor pressure | 0.368-10.5Pa at 25-70℃ | | refractive index | n20/D 1.472(lit.) | | Fp | 350 °F | | storage temp. | Sealed in dry,Room Temperature | | pka | 14.56±0.10(Predicted) | | form | Liquid | | color | Clear white to yellow | | Water Solubility | Soluble in water, 1e+006 mg/L @ 25°C (est), soluble in alcohol and ether. | | InChIKey | PVCJKHHOXFKFRP-UHFFFAOYSA-N | | LogP | -0.117 at 22.2℃ and pH5.4 | | Surface tension | 72.1mN/m at 1g/L and 21.4℃ | | CAS DataBase Reference | 142-26-7(CAS DataBase Reference) | | NIST Chemistry Reference | Acetamide, N-(2-hydroxyethyl)-(142-26-7) | | EPA Substance Registry System | Acetamide, N-(2-hydroxyethyl)- (142-26-7) |
| 2-Acetylaminoethanol Usage And Synthesis |
| Synthesis | 2-Acetylaminoethanol was synthesised by Ethanolamine and methyl acetate stirred and refluxed for 6h. | | Chemical Properties | clear viscous white to yellow liquid | | Uses | 2-Acetylaminoethanol is a humectant recommended for use in emulsions.
| | Uses | It finds its uses as antistatic agent, foam boosting agent, hair conditioning humectant, skin conditioning surfactant and viscosity controlling agent in cosmetics industry. It is a non-tacky glycerine alternative for use in skin and hair care. It has humectant and lubricant properties for use in shampoos, treatment products and hair conditioners. | | Definition | ChEBI: A member of the class of ethanolamines that is 2-aminoethanol in which one of the hydrogens of the amino group is replaced by an acetyl group. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 44, p. 654, 1979 DOI: 10.1021/jo01318a047 |
| 2-Acetylaminoethanol Preparation Products And Raw materials |
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