Aminoacetaldehyde dimethyl acetal

ALDRICH/121967 - 99%

Synonym: 2,2-Dimethoxyethylamine

CAS Number: 22483-09-6
Empirical Formula (Hill Notation): C₄H₁₁NO₂
Molecular Weight: 105.14
EC Number: 245-026-5
MDL Number: MFCD00008135
Linear Formula: NH₂CH₂CH(OCH₃)₂
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-121967-25ML	25 mL	$66.50 1/EAAdd To Favorites		Add To Favorites
45-121967-100ML	100 mL	$176.00 1/EAAdd To Favorites		Add To Favorites
45-121967-500ML	500 mL	$683.00 1/EAAdd To Favorites		Add To Favorites

assay	99%
bp	135-139 °C/95 mmHg (lit.)
density	0.965 g/mL at 25 °C (lit.)
functional group	acetal
	amine
	ether
InChI	1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3
InChI key	QKWWDTYDYOFRJL-UHFFFAOYSA-N
Quality Level	200
refractive index	n20/D 1.417 (lit.)
SMILES string	COC(CN)OC

Application:	Aminoacetaldehyde dimethyl acetal was used in a study to develop a fluorescent substrate for aldehyde dehydrogenase. It 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 efficient 3-step 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. Aminoacetaldehyde dimethyl acetal is used as a building block for the synthesis of various acylated and sufonylated oxyenamides.
Packaging:	25, 100, 500 mL in glass bottle

Symbol	GHS02,GHS05
Signal word	Danger
Hazard statements	H226 - H314
Precautionary statements	P210 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338
Hazard Codes	C
Risk Statements	10-34
Safety Statements	26-36/37/39-45
RIDADR	UN 1993C 3 / PGIII
WGK Germany	WGK 2
Flash Point(F)	111.2 °F - closed cup
Flash Point(C)	44 °C - closed cup