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Merck
CN

470198

2-(Isopropylamino)ethanol

70%

Synonym(s):

N-Isopropylethanolamine

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About This Item

Linear Formula:
(CH3)2CHNHCH2CH2OH
CAS Number:
109-56-8
Molecular Weight:
103.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24870646
MDL number:
MFCD00041755
Beilstein/REAXYS Number:
1633453

Key Documents

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Product Name

2-(Isopropylamino)ethanol, 70%

InChI

1S/C5H13NO/c1-5(2)6-3-4-7/h5-7H,3-4H2,1-2H3

SMILES string

CC(C)NCCO

InChI key

RILLZYSZSDGYGV-UHFFFAOYSA-N

assay

70%

impurities

30% N-isopropyl-2,2′-iminodiethanol

refractive index

n20/D 1.441 (lit.)

bp

172 °C (lit.)

density

0.897 g/mL at 25 °C (lit.)

functional group

amine
hydroxyl

Quality Level

100

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Application

2-(Isopropylamino)ethanol may be used in the synthesis of heterocyclic N,O-acetals.

General description

2-(Isopropylamino)ethanol is a secondary amine. The solubility of CO2 in aqueous solutions of 2-(isopropylamino)ethanol (IPAE) has been evaluated.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

172.4 °F - closed cup

flash_point_c

78 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ2759
MKCZ2478
MKCV1827
MKCT7230
MKCK9815

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E Menegola et al.
Reproductive toxicology (Elmsford, N.Y.), 12(3), 371-374 (1998-06-17)
Previously, postcoital antifertility effects of a number of aminoalcohols, including 2-(isopropylamino)-ethanol, have been demonstrated in rodents. In this experiment, we compared the antifertility activity of 2-(isopropylamino)-ethanol to the following analogs: hydroxyethylpiperidine, hydroxyethylpiridine, hydroxyethylpirrolidine, and hydroxyethylpirrolidone. Female rats were gavaged on
Saba S, et al.
Journal of Chemical Education, 84, 1011-1011 (2007)
L S Borman
In vitro, 18(2), 129-140 (1982-02-01)
The choline analog, N-isopropylethanolamine (IPE), inhibits the growth of both Chinese hamster ovary CHO-K1 and mouse L-M cells by two kinetically distinct mechanisms; I, a reversible and concentration-dependent reduction in the logarithmic population doubling rate and the saturation density of
CO2 solubility and species distribution in aqueous solutions of 2-(isopropylamino) ethanol and its structural isomers.
Yamada H, et al.
International Journal of Greenhouse Gas Control, 17, 99-105 (2013)

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