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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
Orapan Paecharoenchai et al.
AAPS PharmSciTech, 13(4), 1302-1308 (2012-09-26)
The aim of this study was to investigate the transfection efficiency of cationic liposomes formulated with phosphatidylcholine (PC) and novel synthesized diethanolamine-based cationic lipids at a molar ratio of 5:1 in comparison with Lipofectamine™ 2000. Factors affecting transfection efficiency and
G Libralato et al.
Journal of hazardous materials, 176(1-3), 535-539 (2009-12-22)
Monoethanolamine (MEA), diethanolamine (DEA) and triethanolamine (TEA) are compounds with potential acute, sub-chronic and chronic toxicity effects towards aquatic species. A literature review highlighted the existence of a gap in the knowledge on their toxicity with saltwater testing species. A
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
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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