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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
238-396-4
MDL number:
Assay:
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
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
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
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)
Benjamin Boëns et al.
Nucleosides, nucleotides & nucleic acids, 31(3), 197-205 (2012-02-24)
This work deals with the synthesis of a new nitrogen mustard derivative based on thymine. To introduce the bis(2-chloroethyl)amine group to position 4 of the pyrimidine base, many strategies were explored and the desired compound was finally obtained, thanks to
Corneliu N Craciunescu et al.
Toxicological sciences : an official journal of the Society of Toxicology, 107(1), 220-226 (2008-10-25)
Diethanolamine (DEA) is a common ingredient of personal care products. Dermal administration of DEA diminishes hepatic stores of the essential nutrient choline and alters brain development. We previously reported that 80 mg/kg/day of DEA during pregnancy in mice reduced neurogenesis
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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