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470228

Sigma-Aldrich

1-Dimethylamino-2-propanol solution

77 wt. % in H2O

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About This Item

Linear Formula:
(CH3)2NCH2CH(OH)CH3
CAS Number:
108-16-7
Molecular Weight:
103.16
MDL number:
MFCD00004532
UNSPSC Code:
12352100
PubChem Substance ID:
24870648

concentration

77 wt. % in H2O

refractive index

n20/D 1.42

bp

96 °C

density

0.913 g/mL at 25 °C

SMILES string

CC(O)CN(C)C

InChI

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

Inchi Key

NCXUNZWLEYGQAH-UHFFFAOYSA-N

replaced by

Product No.
Description
Pricing

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

95.9 - 99.0 °F - closed cup

flash_point_c

35.5 - 37.2 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
17221JR
10204BR
04612HR

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Kinetics of carbon dioxide (CO 2) with ethylenediamine, 3-amino-1-propanol in methanol and ethanol, and with 1-dimethylamino-2-propanol and 3-dimethylamino-1-propanol in water using stopped-flow technique
Kadiwala S, et al.
Chemical Engineering Journal, 179, 262-271 (2012)
Soluble Ni II alkoxides based on dimethylaminoisopropoxide ligands: molecular structure of [Li (Pr i OH) Ni (η 2-OR)2 Cl]2 and of cis-NiCl2 (ROH)2 (R= CHMeCH2NMe2).
Hubert-Pfalzgraf LG, et al.
Polyhedron, 16(24), 4197-4203 (1997)
S A Naujokaitis et al.
Journal of pharmaceutical sciences, 73(1), 34-39 (1984-01-01)
The structure-activity relationships of 2-dimethylaminoethanol and its analogues as protectors against mechlorethamine cytotoxicity and as inhibitors of choline uptake were evaluated. Of a series of inhibitors and protectors, 2-dimethylaminoethanol was the most potent inhibitor of choline uptake and the most
Synthesis and molecular structures of cobalt (II) ?-diketonate complexes as new MOCVD precursors for cobalt oxide films.
Pasko S, et al.
Polyhedron, 23(5), 735-741 (2004)
Zhaopin Bai et al.
Inorganic chemistry, 49(19), 9005-9011 (2010-09-04)
A new pathway by means of transetherification has been developed to synthesize novel unsymmetrical 2,3,9,10,16,17,23-heptakis(alkoxyl)-24-mono(dimethylaminoalkoxyl)phthalocyanine compounds. Cyclic tetramerization of 4,5-di(alkoxyl)phthalonitrile in refluxing dimethylamino-alcohol with high boiling point such as dimethylaminoethanol (DMAE) and 1-dimethylamino-2-propanol in the presence of lithium and pyrazino[2,3-f][1,10]phenanthroline-2,3-dicarbonitrile
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