22483-09-6 Aminoacetaldehyde dimethyl acetal AKSci J20028
 
 
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  J20028    AKSci Bulk Reagent
Aminoacetaldehyde dimethyl acetal, 99% (GC)
 
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:99% (GC)
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. 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 April 19, 2024


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CATEGORIES
 Aryl and Aliphatic Building Blocks > Amines, Ethers, Acetals


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