209287
Diethanolamine hydrochloride
98%
Synonym(s):
2,2′-Iminodiethanol hydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
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%
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
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)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
A new synthesis of N-monophenylpiperazine.
Pollard CB and MacDowell LG.
Journal of the American Chemical Society, 56(10), 2199-2200 (1934)
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