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2-(tert-Butylamino)ethanol

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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
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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)
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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
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

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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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