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About This Item
Linear Formula:
NH[CH2CH(OH)CH3]2
CAS Number:
Molecular Weight:
133.19
EC Number:
203-820-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
605363
MDL number:
assay
95%
bp
249-250 °C/745 mmHg (lit.)
mp
42-45 °C (lit.)
solubility
alcohol: miscible, hydrocarbons: insoluble, toluene: slightly soluble, water: miscible
density
1.004 g/mL at 25 °C (lit.)
SMILES string
CC(O)CNCC(C)O
InChI
1S/C6H15NO2/c1-5(8)3-7-4-6(2)9/h5-9H,3-4H2,1-2H3
InChI key
LVTYICIALWPMFW-UHFFFAOYSA-N
General description
Bis(2-hydroxypropyl)amine(Diisopropanolamine) is a flexible amino-alcohol ligand and induces the dimerisation of two trinuclear FeIII complexes to form the hexanuclear clusters.
Application
Bis(2-hydroxypropyl)amine(Diisopropanolamine) was used during the sulfinol process to remove sour gases such as hydrogen sulfide and carbonyl sulfide from natural gas.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
275.0 °F - closed cup
flash_point_c
135 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Leigh F Jones et al.
Dalton transactions (Cambridge, England : 2003), (20)(20), 3344-3352 (2005-09-30)
The synthesis, crystal structures and magnetic properties of two hexanuclear Fe(6) clusters of general formula [Fe(6)(O)(2)(OH)(2)(O(2)CR)(10)(dipaH(2))(2)].xMeCN.yH(2)O (R = Ph, x= 5.5, y= 1 (1), R = C(Me)(3), x= 2, y= 3 (2)) are reported. The presence of the flexible amino-alcohol
L M Gieg et al.
Canadian journal of microbiology, 45(5), 377-388 (1999-08-14)
Diisopropanolamine (DIPA) is a "sweetening agent" used to remove hydrogen sulfide from sour natural gas, and it is a contaminant at some sour gas treatment facilities in western Canada. To investigate the biodegradation of this alkanolamine, 14C-DIPA was used in
K A Johnson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45(10), 1838-1845 (2007-05-18)
The repeated dose oral and dermal toxicity of diisopropanolamine (DIPA) was evaluated in rats and compared to the reported toxicity of the related secondary alcohol amine, diethanolamine (DEA). Fischer 344/DuCrl rats were given up to 750 mg/kg/day by dermal application
Two cases of contact dermatitis due to diisopropanolamine.
Yoshihiro Umebayashi
The Journal of dermatology, 32(2), 145-146 (2005-05-24)
W T Stott et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46(2), 761-766 (2007-11-09)
Aminoalcohols differ in mammalian toxicity at least in part based upon their ability to alter the metabolism of phospholipids and to cause depletion of the essential nutrient choline in animals. This study examined the incorporation of diisopropanolamine (DIPA) into phospholipids
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