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About This Item
Linear Formula:
NH[CH2CH(OH)CH3]2
CAS Number:
Molecular Weight:
133.19
Beilstein/REAXYS Number:
605363
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
assay
≥98.0% (T)
form
solid
impurities
≤1% water
bp
249-250 °C/745 mmHg (lit.)
mp
42-45 °C (lit.)
solubility
H2O: miscible
alcohol: miscible
density
1.004 g/mL at 25 °C (lit.)
functional group
amine
hydroxyl
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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Related Categories
Application
Bis(2-hydroxypropyl)amine (Diisopropanolamine) was used to study its effects upon choline uptake and phospholipid synthesis in Chinese hamster ovary (CHO) cells.
signalword
Warning
hcodes
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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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
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
K Yamamoto et al.
Carcinogenesis, 10(9), 1607-1611 (1989-09-01)
The carcinogenic activity of endogenously synthesized N-nitrosobis(2-hydroxypropyl)amine (BHP) was investigated in male Wistar rats administered bis(2-hydroxypropyl)amine (BHPA) mixed in powder diet at a concentration of 1%, and sodium nitrite (SN) dissolved in distilled water at concentrations of 0.15 and 0.3%
Two cases of contact dermatitis due to diisopropanolamine.
Yoshihiro Umebayashi
The Journal of dermatology, 32(2), 145-146 (2005-05-24)
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