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Merck
CN

471518

2-(tert-Butylamino)ethanol

99%

Synonym(s):

N-tert-Butylethanolamine

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About This Item

Linear Formula:
(CH3)3CNHCH2CH2OH
CAS Number:
4620-70-6
Molecular Weight:
117.19
EC Number:
225-034-5
UNSPSC Code:
12352100
PubChem Substance ID:
24870739
Beilstein/REAXYS Number:
1732684
MDL number:
MFCD00002837

Key Documents

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InChI key

IUXYVKZUDNLISR-UHFFFAOYSA-N

InChI

1S/C6H15NO/c1-6(2,3)7-4-5-8/h7-8H,4-5H2,1-3H3

SMILES string

CC(C)(C)NCCO

vapor density

4 (vs air)

assay

99%

form

solid

bp

90-92 °C/25 mmHg (lit.)

mp

41-43 °C (lit.)

density

0.867 g/mL at 25 °C (lit.)

General description

2-(tert-Butylamino)ethanol (TBAE) is an alkanolamine. Its dissociation constant has been evaluated at several temperatures. It is a sterically hindered amine and is a useful chemical absorbent for the selective absorption of hydrogen sulfide in the presence of carbon dioxide. The physical solubility of hydrogen sulfide in aqueous solutions of TBAE neutralized with hydrochloric acid has been tested. The obtained solubility data was correlated using the van-Krevelen-Hoftijzer method.

Application

2-(tert-Butylamino)ethanol may be used in the synthesis of 3-tert-butyl-2,2-diphenyl-1,3-oxazaborolidine.

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
11414PI
04512HR

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Physical solubility of hydrogen sulfide in aqueous solutions of 2-(tert-butylamino) ethanol.
Munder B, et al.
Journal of Chemical and Engineering Data, 45(6), 1201-1204 (2000)
Dissociation constants of some alkanolamines at 293, 303, 318, and 333 K.
Little RJ, et al.
Journal of Chemical and Engineering Data, 35(3), 276-277 (1990)
Yuliya Dobrydneva et al.
Molecular pharmacology, 69(1), 247-256 (2005-10-11)
We have synthesized a series of 2-aminoethoxydiphenyl borate (2-APB, 2,2-diphenyl-1,3,2-oxazaborolidine) analogs and tested their ability to inhibit thrombin-induced Ca(2+) influx in human platelets. The analogs were either synthesized by adding various substituents to the oxazaborolidine ring (methyl, dimethyl, tert-butyl, phenyl
Effect of carbon dioxide loading on the solubility of nitrous oxide in aqueous solutions of 2-(tert-butylamino) ethanol.
Munder B, et al.
Journal of Chemical and Engineering Data, 45(6), 1195-1195 (2000)

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