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Merck

209287

Diethanolamine hydrochloride

98%

Synonym(s):

2,2′-Iminodiethanol hydrochloride

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About This Item

Linear Formula:
(HOCH2CH2)2NH · HCl
CAS Number:
14426-21-2
Molecular Weight:
141.60
NACRES:
NA.22
PubChem Substance ID:
24852562
UNSPSC Code:
12352100
EC Number:
238-396-4
MDL number:
MFCD00012595

Product Name

Diethanolamine hydrochloride, 98%

InChI key

VJLOFJZWUDZJBX-UHFFFAOYSA-N

InChI

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

SMILES string

Cl.OCCNCCO

assay

98%

refractive index

n20/D 1.517 (lit.)

density

1.261 g/mL at 25 °C (lit.)

functional group

amine
hydroxyl

Quality Level

200

Related Categories

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

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9753
BCCM4524
BCCK8827
BCCJ6222
BCCD9430

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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)
Valentyna V Semenaka et al.
Inorganic chemistry, 49(12), 5460-5471 (2010-06-15)
Two new tetranuclear complexes, [Zn(2)Cr(2)(NCS)(4)(Dea)(2)(HDea)(2)].4DMSO (1; DMSO = dimethyl sulfoxide) and [Zn(2)Cr(2)(NCS)(4)(Dea)(2)(HDea)(2)].2CH(3)CN (2), were prepared from zinc oxide, Reinecke's salt, NH(4)[Cr(NCS)(4)(NH(3))(2)].H(2)O, ammonium thiocyanate, and a nonaqueous solution of diethanolamine (H(2)Dea) in a reaction carried out under open air. Both compounds
Bjørn Henrik Hansen et al.
Aquatic toxicology (Amsterdam, Netherlands), 99(2), 212-222 (2010-06-12)
Alkanolamines are surface-active chemicals used in a wide range of industrial, agricultural and pharmaceutical applications and products. Of particular interest is the use of alkanolamines such as diethanolamine (DEA) in the removal of CO(2) from natural gas and for CO(2)
A Durán-Moreno et al.
Journal of hazardous materials, 186(2-3), 1652-1659 (2011-01-11)
The aim of this work was to evaluate the efficiency of three chemical oxidation processes for increasing the biodegradability of aqueous diethanolamine solutions (aqueous DEA solutions), to be used as pre-treatments before a biological process. The raw aqueous DEA solution
Daniel R Fandrick et al.
Organic letters, 11(23), 5458-5461 (2009-11-03)
The utility of propargyl diethanolamine boronates as reagents for the preparation of allenes and homopropargylic alcohols is presented. Protonolysis with TFA and electrophilic substitution with N-halosuccinimides proceeded with inversion to provide the corresponding allene in high yield and regioselectivity. Alternatively
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