2-(tert-Butylamino)ethanol
2-(tert-Butylamino)ethanol Basic information
- Product Name:
- 2-(tert-Butylamino)ethanol
- Synonyms:
-
- 2-[(1,1-dimethylethyl)amino]-ethano
- 2-[(1,1-dimethylethyl)amino]-Ethanol
- beta-tert-Butylaminoethanol
- Ethanol, 2-(tert-butylamino)-
- Ethanol, 2-[(1,1-dimethylethyl)amino]-
- t-butylethanolamine
- 2-((1,1-dimethylethyl)amino)ethanol
- tert-Butylaminoethanol
- CAS:
- 4620-70-6
- MF:
- C6H15NO
- MW:
- 117.19
- EINECS:
- 225-034-5
- Product Categories:
-
- Amino Alcohols
- Building Blocks
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Mol File:
- 4620-70-6.mol
2-(tert-Butylamino)ethanol Chemical Properties
- Melting point:
- 41-43 °C(lit.)
- Boiling point:
- 90-92 °C25 mm Hg(lit.)
- Density
- 0.867 g/mL at 25 °C(lit.)
- vapor density
- 4 (vs air)
- refractive index
- 1.4444 (estimate)
- Flash point:
- 156 °F
- storage temp.
- Store below +30°C.
- form
- low melting solid
- pka
- 14.81±0.10(Predicted)
- InChI
- InChI=1S/C6H15NO/c1-6(2,3)7-4-5-8/h7-8H,4-5H2,1-3H3
- InChIKey
- IUXYVKZUDNLISR-UHFFFAOYSA-N
- SMILES
- C(O)CNC(C)(C)C
- CAS DataBase Reference
- 4620-70-6(CAS DataBase Reference)
- EPA Substance Registry System
- Ethanol, 2-[(1,1-dimethylethyl)amino]- (4620-70-6)
Safety Information
- Hazard Codes
- C
- Risk Statements
- 21-34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 2923 8/PG 2
- WGK Germany
- 3
- RTECS
- KK7177500
- F
- 9
- HS Code
- 2922 19 00
- HazardClass
- 8
- PackingGroup
- II
- Toxicity
- LD50 orally in Rabbit: 1620 mg/kg LD50 dermal Rabbit 635 mg/kg
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
2-(tert-Butylamino)ethanol Usage And Synthesis
Chemical Properties
white solid or crystalline needles
Uses
2-(tert-Butylamino)ethanol is used in the catalytic carbonylation of aliphatic amines to beta-lactams.
Hazard
Moderately toxic by ingestion and skin con- tact. A severe eye irritant.
Research
A sterically hindered alkanol amine, 2-(tertbutylamino)ethanol (TBAE), was reported to be able to reversibly interact with CO2 in a 1/1 molar ratio exclusively through its ?OH group, producing zwitterionic carbonate species in 30% ethylene glycol (EG) solution of TBAE but not carbamate or bicarbonate that can be produced by the prototypical amines[1].
References
[1] Hong-Bin Xie. “CO2 Absorption in an Alcoholic Solution of Heavily Hindered Alkanolamine: Reaction Mechanism of 2-(tert-Butylamino)ethanol with CO2 Revisited.” The Journal of Physical Chemistry A 119 24 (2015): 6346–6353.
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