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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

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

172.4 °F - closed cup

Flash Point(C)

78 °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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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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