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Aminoacetaldehyde dimethyl acetal, 99%
CAS: 22483-09-6 | C4H11NO2 | 105.137 g/mol
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Catalog number A15498.36
also known as A15498-36
Price (TWD)
-
Quantity:
500 g
Chemical Identifiers
CAS22483-09-6
IUPAC Name2,2-dimethoxyethan-1-amine
Molecular FormulaC4H11NO2
InChI KeyQKWWDTYDYOFRJL-UHFFFAOYSA-N
SMILESCOC(CN)OC
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.5%
Refractive Index1.4155-1.4180 @ 20°C
FormLiquid
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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
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.
Solubility
Miscible in water. Soluble in chloroform, methanol.
Notes
Store in a cool, dry conditions in a well sealed container. Incompatible with oxidizing agent.
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.
Solubility
Miscible in water. Soluble in chloroform, methanol.
Notes
Store in a cool, dry conditions in a well sealed container. Incompatible with oxidizing agent.
RUO – Research Use Only
General References:
- R W Storms; A P Trujillo; J B Springer; L Shah; O M Colvin; S M Ludeman; C Smith. Isolation of primitive human hematopoietic progenitors on the basis of aldehyde dehydrogenase activity. PNAS. 1999, 96 (16), 9118-9123.
- Hitoshi Sashiwa; Hirufumi Yajima; Sei-ichi Aiba. Synthesis of a chitosan-dendrimer hybrid and its biodegradation. Biomacromolecules. 2003, 4 (5), 1244-1249.