Substance

ID:335198

Aminoacetaldehyde dimethyl acetal

Names and Identifiers
IUPAC name
2,2-dimethoxyethan-1-amine
IUPAC Traditional name
2,2-dimethoxyethanamine
Synonyms
2,2-二甲氧基乙胺Aminoacetaldehyde dimethyl acetal氨基乙醛缩二甲醇2,2-Dimethoxyethylamine
Registration numbers
CAS Number
EC Number
MDL Number
Beilstein Number
PubChem SID
Properties
Safety Information
GHS Pictograms
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS05
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
UN Number
1993
Packing Group
3
GHS Signal Word
Danger
GHS Precautionary statements
P280-P305+P351+P338-P310
European Hazard Symbols
Corrosive Corrosive (C)
GHS Hazard statements
H226-H314
Risk Statements
10-34
Safety Statements
26-36/37/39-45
Hazard Class
3
MSDS Link
RID/ADR
UN 1993 3/PG 3
German water hazard class
2
Product Information
Linear Formula
NH2CH2CH(OCH3)2
Purity
99%
Physical Property
Density
0.965 g/mL at 25 °C(lit.)
Flash Point
44 °C
111.2 °F
Refractive Index
n20/D 1.417(lit.)
Boiling Point
135-139 °C/95 mmHg(lit.)
Molecule Details
Application
Used in an efficient 3-step synthesis of a bicyclic proline analog from L-ascorbic acid.1 Also used in a 3-component reaction catalyzed by MgClO4 leading to α-aminophosphonates.2
Packaging
25, 100, 500 mL in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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