Name | Aminoacetaldehyde dimethyl acetal |
Synonyms | anjiahuanchun 2,2-Dimethyethanamine 2,2-Dimethoxyethylamin 2,2-dimethoxyethanamine 2,2-Dimetoxyethyl Amine 2,2-Dimethoxyethylamine Glycinal dimethyl acetal 2,2-dimethoxyethanaminium Aminoacetaldehyde dimethyl ace Aminoacetaldehyd Dimethy Acetal AMINOACETOLDEHYDE DIMETHYL ACETOL Aminoacetaldehyde dimethyl acetal 2-aminoacetaldehyde dimethyl acetal |
CAS | 22483-09-6 |
EINECS | 245-026-5 |
InChI | InChI=1/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3/p+1 |
InChIKey | QKWWDTYDYOFRJL-UHFFFAOYSA-N |
Molecular Formula | C4H11NO2 |
Molar Mass | 105.14 |
Density | 0.965 g/mL at 25 °C (lit.) |
Melting Point | -78°C |
Boling Point | 135-139 °C/95 mmHg (lit.) |
Flash Point | 128°F |
Water Solubility | miscible |
Vapor Presure | 8.66mmHg at 25°C |
Appearance | Liquid |
Color | Clear colorless to pale yellow |
BRN | 741868 |
pKa | 6.95±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
Refractive Index | n20/D 1.417(lit.) |
Use | Used as a pharmaceutical Intermediate |
Risk Codes | R10 - Flammable R34 - Causes burns R36/37/38 - 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. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S16 - Keep away from sources of ignition. S36 - Wear suitable protective clothing. |
UN IDs | UN 1993 3/PG 3 |
WGK Germany | 2 |
TSCA | Yes |
HS Code | 29225000 |
Hazard Note | Flammable/Corrosive |
Hazard Class | 3 |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
introduction | aminoacetaldehyde dimethanol is a valuable primary amine compound. amino functional group is a very active active group, which can undergo salt and amidation reactions. it is an important intermediate for the synthesis of ivabradine hydrochloride, proline analogs, amino phosphate esters and other drugs, and has a very wide range of applications in the fields of chemistry, chemical industry, medicine and so on. |
Uses | Aminoacetaldehyde dimethanol is a valuable primary amine compound. Amino functional group is a very active active group, which can undergo salt and amidation reactions. It is an important intermediate for the synthesis of ivabradine hydrochloride, proline analogs, aminophosphate and other drugs. It has a very wide range of applications in the fields of chemistry, chemical industry, medicine and so on. Used as a pharmaceutical intermediate Used in the effective synthesis of proline analogs from ascorbic acid through a 3-step reaction; also used in the preparation of phosphonate by a 3-component reaction catalyzed by MgClO4 |
preparation | using chloroacetaldehyde dimethanol as raw material, solvent methanol, high temperature and high pressure in 28% ammonia water can obtain aminoacetaldehyde dimethanol. |