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470198

Sigma-Aldrich

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
Beilstein:
1633453
MDL number:
MFCD00041755
UNSPSC Code:
12352100
PubChem Substance ID:
24870646
NACRES:
NA.22

Quality Level

100

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.)

SMILES string

CC(C)NCCO

InChI

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

InChI key

RILLZYSZSDGYGV-UHFFFAOYSA-N

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General description

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

Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Saba S, et al.
Journal of Chemical Education, 84, 1011-1011 (2007)
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
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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