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| 2,2-Dimethoxyethylamine Basic information |
| Product Name: | 2,2-Dimethoxyethylamine | | Synonyms: | AMINOACETOLDEHYDE DIMETHYL ACETOL;2,2-Dimetoxyethyl Amine;2,2-Dimethoxyethylamin;Glycinal dimethyl acetal;Aminoacetaldehyd Dimethy Acetal;Aminoacetaldehyde dimethyl ace;anjiahuanchun;Aminoacetaldehyde dimethyl acetal ,98% | | CAS: | 22483-09-6 | | MF: | C4H11NO2 | | MW: | 105.14 | | EINECS: | 245-026-5 | | Product Categories: | Pharmaceutical Intermediates;1 | | Mol File: | 22483-09-6.mol |
| 2,2-Dimethoxyethylamine Chemical Properties |
| Hazard Codes | C,F,Xi | | Risk Statements | 10-34-36/37/38 | | Safety Statements | 26-36/37/39-45-16-36 | | RIDADR | UN 1993 3/PG 3 | | WGK Germany | 2 | | Hazard Note | Flammable/Corrosive | | TSCA | Yes | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29225000 |
| 2,2-Dimethoxyethylamine Usage And Synthesis |
| Chemical Properties | clear colorless to pale yellow liquid | | Uses | Amino acetaldehyde dimethyl was used in preparation of chitosan- dendrimer hybrids having various functional groups such as carboxyl, ester and poly(ethylene glycol). It was used in an synthesis of a bicyclic proline analog from L-ascorbic acid and in 3-component reaction catalyzed by MgClO4 leading to α-aminophosphonates. | | General Description | Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine. | | Purification Methods | Dry the acetal over KOH pellets and distil it through a 30cm vacuum jacketed Vigreux column (p 11). [Lawson J Am Chem Soc 75 3398 1953, Erickson et al. J Am Chem Soc 77 6640 1955, Beilstein 4 IV 1918.] |
| 2,2-Dimethoxyethylamine Preparation Products And Raw materials |
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