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| | (S)-(+)-1-Amino-2-propanol Basic information |
| | (S)-(+)-1-Amino-2-propanol Chemical Properties |
| Melting point | 24-26 °C(lit.) | | alpha | 18 º (c=1.8, H2O) | | Boiling point | 160 °C(lit.) | | density | 0.954 g/mL at 25 °C(lit.) | | vapor density | 2.6 (vs air) | | vapor pressure | <1 mm Hg ( 20 °C) | | refractive index | n20/D 1.4437(lit.) | | Fp | 169 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Sparingly), Water (Sparingly) | | pka | 12.92±0.35(Predicted) | | form | Liquid After Melting | | color | Clear colorless to pale yellow | | Specific Gravity | 0.954 | | Optical Rotation | [α]20/D +18°, c = 1.8 in H2O | | Water Solubility | soluble | | Sensitive | Hygroscopic | | BRN | 1718868 | | Cosmetic Ingredient Review (CIR) | (S)-(+)-1-Amino-2-propanol (2799-17-9) | | InChI | 1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3/t3-/m0/s1 | | InChIKey | HXKKHQJGJAFBHI-VKHMYHEASA-N | | SMILES | C[C@H](O)CN | | LogP | -1.127 (est) | | CAS DataBase Reference | 2799-17-9(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Propanol, 1-amino-, (S)-(2799-17-9) |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 23-26-36-45 | | RIDADR | UN 3259 8/PG 2 | | WGK Germany | 1 | | RTECS | UA5775000 | | F | 10-34 | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29221980 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Skin Corr. 1B |
| | (S)-(+)-1-Amino-2-propanol Usage And Synthesis |
| Chemical Properties | colorless to light yellow liquid | | Uses | Emulsifying agent, drycleaning soaps, soluble
textile oils, wax removers, metal-cutting oils, cosmetics, emulsion paints, plasticizers, insecticides. | | Uses | (S)-(+)-1-Amino-2-propanol may be used in the preparation of S-(+)-1-(2,3-naphthalimido)-2-propanol. | | General Description | (S)-(+)-1-Amino-2-propanol is a chiral amino alcohol. | | Synthesis | Step (1): dissolve sodium tert-butoxide (230g, 2.39mol) in tetrahydrofuran (2L), slowly add trifluoroacetamide (226g, 2mol) under the ice bath, stirring for 30min; then add S-epoxypropane (128g, 2.2mol) under the ice bath, naturally warmed to room temperature, and continue to stir the reaction for 10h, and then stirred the reaction for another 2h at 35; after the reaction After the reaction, 2N (equivalent concentration) of hydrochloric acid was added dropwise to the system for neutralization, and then 1L of water was added, static layering, the aqueous phase was extracted with dichloromethane, the organic phases were combined, dried with anhydrous sodium sulfate, and concentrated under pressure to obtain a total of 318g of intermediate product I, with a yield of 93%. Step (2): dissolve the intermediate product I (310g, 1 .81mol) obtained in step (1) in methanol (1 .5L), add 200mL of water and potassium carbonate (550g, 4mol), stirring at room temperature for 6h, filtration, concentration to dryness, the product obtained was dissolved in dichloromethane, filtration, insoluble matter was removed, anhydrous sodium sulfate was dried, concentration, distillation under reduced pressure, the target product S 1-amino-2-propanol totaling 122 g in 90% yield. |
| | (S)-(+)-1-Amino-2-propanol Preparation Products And Raw materials |
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