2,2-Diethoxyethylamine
2,2-Diethoxyethylamine Basic information
- Product Name:
- 2,2-Diethoxyethylamine
- Synonyms:
-
- 2,2-diethoxy-ethanamin
- 2,2-Diethoxyethanamine
- 2,2-Diethyloxyethylamine
- Acetaldehyde, amino-, diethyl acetal
- 1-AMINO-2,2-DIETHOXYETHANE
- AMINOACETAL
- AMINOACETALDEHYDE DIETHYL ACETAL
- B-AMINOACETAL
- CAS:
- 645-36-3
- MF:
- C6H15NO2
- MW:
- 133.19
- EINECS:
- 211-439-4
- Product Categories:
-
- Pharmaceutical Intermediates
- Small molecule
- bc0001
- Mol File:
- 645-36-3.mol
2,2-Diethoxyethylamine Chemical Properties
- Melting point:
- -78
- Boiling point:
- 162-163 °C (lit.)
- Density
- 0.916 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.417(lit.)
- Flash point:
- 114 °F
- storage temp.
- Keep in dark place,Inert atmosphere,2-8°C
- solubility
- Chloroform (Slightly), Ethyl Acetate (Slightly)
- pka
- pK1:8.47(+1) (25°C)
- form
- clear liquid
- color
- Colorless to Light yellow
- Water Solubility
- soluble
- BRN
- 506067
- InChI
- 1S/C6H15NO2/c1-3-8-6(5-7)9-4-2/h6H,3-5,7H2,1-2H3
- InChIKey
- HJKLEAOXCZIMPI-UHFFFAOYSA-N
- SMILES
- CCOC(CN)OCC
- CAS DataBase Reference
- 645-36-3(CAS DataBase Reference)
- NIST Chemistry Reference
- Ethanamine, 2,2-diethoxy-(645-36-3)
- EPA Substance Registry System
- Ethanamine, 2,2-diethoxy- (645-36-3)
Safety Information
- Hazard Codes
- Xi,C,F
- Risk Statements
- 10-36/37/38-34
- Safety Statements
- 23-24/25-26-45-36/37/39-16-36
- RIDADR
- UN 1989 3/PG 3
- WGK Germany
- 3
- Hazard Note
- Irritant
- TSCA
- TSCA listed
- HazardClass
- 3
- PackingGroup
- III
- HS Code
- 29225090
- Storage Class
- 3 - Flammable liquids
- Hazard Classifications
- Eye Dam. 1
Flam. Liq. 3
Skin Corr. 1B
MSDS
- Language:English Provider:2,2-Diethoxyethylamine
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2,2-Diethoxyethylamine Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS TO LIGHT YELLOW LIQUID
Uses
Aminoacetaldehyde diethyl acetal, is used as an agrochemical intermediate, pharmaceutical, syntheses material intermediate.
Synthesis
There are two main methods of synthesizing aminoacetaldehyde diethyl acetal as follows:
(1) 2-(2-azidoethyl)-1,3-dioxolane is generated from 2-(2-azidoethyl)-1,3-dioxolane by refluxing 2-(2-azidoethyl)-1,3-dioxolane with sodium azide over a phase transfer catalyst, which is further reacted with triphenylphosphine/water, but the NaN3 compounds are highly poisonous and explosive, which is not conducive to industrialized production.
(2) 2-(2-bromoethyl)-1,3-dioxolane is obtained by ion exchange with a macroporous quaternary ammonium Amberlite resin ( AmberliteIRA 900) that has been attached to a negative nitrite ion to obtain 2-(2-nitrosoethyl)-1,3-dioxolane, which is then catalyzed by platinum oxidation to obtain aminoglycolaldehyde diethyl acetal by platinum oxidation catalyst, which has a low yield.
2,2-Diethoxyethylamine Preparation Products And Raw materials
Raw materials
Preparation Products
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2,2-Diethoxyethylamine(645-36-3)Related Product Information
- 1,1-Dimethoxyethane
- Bromoacetaldehyde dimethyl acetal
- Acrolein diethyl acetal
- Bromoacetaldehyde diethyl acetal
- Aminoacetaldehyde dimethyl acetal
- Diethyl phthalate
- 2-(4-Aminophenyl)ethanol
- 4,4-Diethoxybutylamine
- Chloroacetaldehyde diethyl acetal
- 2-(2-Aminothiazol-4-yl)glyoxylic acid
- Monoethanolamine
- 3,3-Diethoxypropionitrile
- Acetylacetaldehyde dimethyl acetal
- Acetal
- Diethyl malonate
- 2,6-DI-TERT-BUTYLNAPHTHALENE SULFONIC ACID SODIUM SALT
- Trimethylstearylammonium Chloride
- Benzyl carbamate