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Key Documents

209287

Sigma-Aldrich

Diethanolamine hydrochloride

98%

Synonym(s):

2,2′-Iminodiethanol hydrochloride

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About This Item

Linear Formula:
(HOCH2CH2)2NH · HCl
CAS Number:
Molecular Weight:
141.60
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.517 (lit.)

density

1.261 g/mL at 25 °C (lit.)

functional group

amine
hydroxyl

SMILES string

Cl.OCCNCCO

InChI

1S/C4H11NO2.ClH/c6-3-1-5-2-4-7;/h5-7H,1-4H2;1H

InChI key

VJLOFJZWUDZJBX-UHFFFAOYSA-N

Application

Diethanolamine hydrochloride was used in the synthesis of:
  • N-monophenylpiperazine
  • diethanolammonium chloride, required for the preparation of diethanolammonium-tetrachloridopalladate(II) complex

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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A new synthesis of N-monophenylpiperazine.
Pollard CB and MacDowell LG.
Journal of the American Chemical Society, 56(10), 2199-2200 (1934)
Siou-Yin Chen et al.
Inorganic chemistry, 51(8), 4448-4457 (2012-04-05)
The synthesis, X-ray crystallography, magnetic properties, and high-field electron paramagnetic resonance (HFEPR) of a new heptanuclear manganese complex [Mn(7)(heamp)(6)](ClO(4))(2)·4CH(2)Cl(2)·H(2)O (complex 2), in which heampH(3) is 2-[N,N-di(2-hydroxyethyl)aminomethyl]phenol (compound 1), is reported. Complex 2 has a hexagonal, disk-shaped topology and contains six
A R W Smith et al.
Journal of applied microbiology, 105(6), 2161-2168 (2009-01-06)
This study investigates the effects of N-(n-dodecyl)diethanolamine (DDA) on enzymes and growing cells of Escherichia coli NCIMB 8277. Enzyme activities in the presence of DDA were determined by measuring substrate-dependent oxygen consumption by whole cells, or of NADH formation or
Pingsong Wu et al.
Chemistry & biodiversity, 5(10), 1913-1926 (2008-10-31)
Vanadate-dependent peroxidases contain, in their active center, vanadate covalently attached to histidine in an overall trigonal-bipyramidal array. We describe here the synthesis and characterization of optically active amino alcohols and their vanadium(V) complexes, and we show that the structural models
William Conway et al.
Environmental science & technology, 46(13), 7422-7429 (2012-05-25)
The kinetics of the fast reversible carbamate formation reaction of CO(2)(aq) with a series of substituted cyclic secondary amines as well as the noncyclic secondary amine diethanolamine (DEA) has been investigated using the stopped-flow spectrophotometric technique at 25.0 °C. The

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