209287
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
Recommended Products
Quality Level
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
hcodes
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)
Zorica D Petrović et al.
Bioorganic chemistry, 37(5), 162-166 (2009-08-15)
The reaction of PdCl(2) with diethanolammonium chloride (DEAxHCl), in the molar ratio 1:2, affords the [HDEA](2)[PdCl(4)] complex (1). The hydrolytic activity of the novel Pd(II) complex 1 was tested in reaction with N-acetylated L-histidylglycine dipeptide (AcHis-Gly). Complex 1, as well
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)
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
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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