| Lauramidopropyl betaine Chemical Properties |
| Melting point | >128??C (dec.) |
| density | 1.15[at 20??] |
| vapor pressure | 0.31Pa at 20?? |
| storage temp. | Hygroscopic, -20??C Freezer, Under inert atmosphere |
| solubility | Chloroform (Slightly), Methanol (Slightly) |
| form | Solid |
| color | White to Off-White |
| Water Solubility | 250mg/L at 20?? |
| Stability: | Hygroscopic |
| LogP | 3.54 at 20?? |
| EPA Substance Registry System | 1-Propanaminium, N-(carboxymethyl)-N,N-dimethyl-3-[(1-oxododecyl)amino]-, inner salt (4292-10-8) |
| Safety Information |
| MSDS Information |
| Lauramidopropyl betaine Usage And Synthesis |
| Description | Lauramidopropyl betaine is a new type of special amphoteric surfactant, which belongs to the same series as lauramidopropyl betaine, and is a modified derivative of alkyl betaine. Lauramidopropyl betaine has the characteristics of temperature resistance, acid and alkali resistance, good salt resistance, wide isoelectric point and strong viscoelasticity, etc. It is widely used in oil field oil repelling, leather, daily chemical industry and other fields. As a good viscoelastic surfactant applied to the substrate acidification of oilfield, it can effectively reduce the oil/water interfacial tension and improve the recovery rate of tertiary oil recovery. Also it can be used as conditioning agent, wetting agent, bactericide, antistatic agent, emulsifier, thickener and in self-steering acid system for carbonate acidification. |
| Uses | Lauroylamide Propylbetaine is used cosmetic and hair compositions of enhanced viscosity and clarity. |
| Flammability and Explosibility | Not classified |
| Toxicology | Lauramidopropyl betaine (50% component in cocamidopropyl betaine – as a model for cocamidopropyl betaine) is poorly absorbed from the intestinal tract and through the skin. Rinsing the skin after 10 minutes of contact reduces the absorption even further. Following oral or dermal exposure, there is metabolism of the absorbed material, as indicated by the appearance of a more polar compound in the urine and by the liberation of?14CO2. |
