22483-09-6 Aminoacetaldehyde dimethyl acetal AKSci J90664
 
 
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  J90664    AKSci Bulk Reagent
Aminoacetaldehyde dimethyl acetal
, 95%
 
2,2-Dimethoxyethylamine




IDENTITY
CAS Number:22483-09-6
MDL Number:MFCD00008135
MF:C4H11NO2
MW:105.14
EINECS:245-026-5
BRN:741868
SPECIFICATIONS & PROPERTIES
Min. Purity Spec:95%
Physical Form (at 20°C):Liquid
Boiling Point:136°C
Flash Point:44°C
Density:0.97
Refractive Index:1.416-1.418
Long-Term Storage:Store long-term in a cool, dry place
DOT/IATA TRANSPORT INFORMATION
UN #:UN1993
Hazard Class:3; Flammable Liquid
Packing Group:III
A hazmat fee may apply to certain package sizes and shipment methods. Please check pricing table for an indicator of applicable hazmat fees.

REVIEW

 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.

REFERENCES
[1]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.
[2] Hitoshi Sashiwa; Hirufumi Yajima; Sei-ichi Aiba. Synthesis of a chitosan-dendrimer hybrid and its biodegradation. Biomacromolecules. 2003, 4 (5), 1244-1249.

GLOBALLY HARMONIZED SYSTEM (GHS)

Pictograms

Signal Word
Danger

Hazard Statements
H226; H314

Precautionary Statements
P210; P233; P240; P241; P242; P243; P264; P280; P301+P330+P331; P303+P361+P353; P304+P340; P305+P351+P338; P310; P321; P363; P370+P378; P403+P235; P405; P501


Current as of July 22, 2024


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CATEGORIES

 Aryl and Aliphatic Building Blocks > Amines, Ethers, Acetals


PubChem