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133019

Sigma-Aldrich

Bis(2-hydroxypropyl)amine

95%

Synonym(s):

1,1′-Iminodi-2-propanol, Diisopropanolamine

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About This Item

Linear Formula:
NH[CH2CH(OH)CH3]2
CAS Number:
110-97-4
Molecular Weight:
133.19
Beilstein/REAXYS Number:
605363
EC Number:
203-820-9
MDL number:
MFCD00004531
UNSPSC Code:
12352100
PubChem Substance ID:
24848089

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

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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.

replaced by

Product No.
Description
Pricing

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

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

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Certificates of Analysis (COA)

Lot/Batch Number
S38256
06722LW
05601LT
17017BD
11321BN

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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
Uptake of sulfolane and diisopropanolamine (DIPA) by cattails (Typha latifolia).
Doucette WJ, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 81(1), 41-49 (2005)
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
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
Y Konishi et al.
IARC scientific publications, (105)(105), 318-321 (1991-01-01)
The carcinogenic activity of endogenously synthesized N-nitroso-bis(2-hydroxy-propyl)amine (NDHPA) was investigated in male Wistar rats administered bis(2-hydroxypropyl)amine (DHPA), mixed into a powdered diet at a concentration of 1%, and NaNO2 dissolved in distilled water at concentrations of 0.15% and 0.3%, for
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