Weight | 133.191 g/mol |
---|---|
Formula | C6H15NO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
DIISOPROPANOLAMINE
diisopropanolamine hydrochloride · bis(2-hydroxypropyl)amine
110-97-4, 68153-96-8, 90530-07-7
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- Sigma-Aldrich - DIISOPROPANOLAMINE31.40 - 114.00 USD
- Fisher Scientific - Search for DIISOPROPANOLAMINE
- TCI - DIISOPROPANOLAMINE16.00 - 28.00 USD
- Metabolism of the Pancreatic Carcinogens N-Nitroso-bis(2-oxopropyl)amine and N-Nitroso-bis(2-hydroxypropyl)amine in the Syrian Hamster (Journal of the National Cancer Institute, 1976)
- Experimental pancreatic carcinogenesis. I. Morphogenesis of pancreatic adenocarcinoma in the Syrian golden hamster induced by N-nitroso-bis(2-hydroxypropyl)amine. (American Journal of Pathology, 1977)
- Densities, Viscosities, and Surface Tensions of Aqueous Mixtures of Sulfolane + Triethanolamine and Sulfolane + Diisopropanolamine (Journal of Chemical & Engineering Data, 2011)
- Solubility of carbon dioxide in aqueous solutions of diisopropanolamine and methyldiethanolamine (Fluid Phase Equilibria, 2010)
- Solubility of hydrogen sulfide and carbon dioxide in an aqueous diisopropanolamine solution (Journal of Chemical & Engineering Data, 1977)
- Dielectric Constants of Aqueous Diisopropanolamine, Diethanolamine, N-Methyldiethanolamine, Triethanolamine, and 2-Amino-2-methyl-1-propanol Solutions (Journal of Chemical & Engineering Data, 2007)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - diisopropanolamine hydrochloride
- bis(2-hydroxypropyl)amine
-
SMILESCC(CNCC(C)O)O
-
InChIKeyLVTYICIALWPMFW-UHFFFAOYSA-N
- Pubchem - DIISOPROPANOLAMINE
- Wikipedia - diisopropanolamine
Diisopropanolamine is a chemical compound with the molecular formula used as an emulsifier, stabilizer, and chemical intermediate. Diisopropanolamine can be prepared by the reaction of isopropanolamine or ammonia with propylene oxide.
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Similar Compounds
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TERT-BUTYL HYDROPEROXIDE
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(123-96-6, 4128-31-8, 25339-16-6)
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1-tert-butoxy-2-propanol
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2-OCTANOL
(123-96-6, 4128-31-8, 25339-16-6)
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2-PENTENOIC ACID
(626-98-2, 13991-37-2, 27516-53-6)
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(5131-66-8)
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beta-Hydroxyisovaleric acid
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26543-05-5
(2068-83-9, 26543-05-5)
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(54972-97-3, 69203-06-1, 37769-60-1, 626-93-7)
3 alternate names
3 suppliers
3-METHYL-2-BUTANOL
(6032-29-7, 598-75-4)
3 alternate names
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(594-61-6)
3 alternate names
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(4026-18-0, 600-37-3)
3 alternate names
3 suppliers
2-Hydroxy-4-methylpentanoic acid
(498-36-2, 10303-64-7)
3 alternate names
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Dowfroth 250
(54004-82-9, 20324-32-7, 1320-67-8, 37286-64-9)
3 alternate names
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13748-90-8
(13748-90-8)
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2-Butoxyacetic acid
(2516-93-0)
3 alternate names
3 suppliers
trans-2-Pentenoic acid
(626-98-2, 13991-37-2, 27516-53-6)
3 alternate names
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3-METHYLCYCLOHEXANOL
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trans-2-Hexenoic acid
(1289-40-3, 13419-69-7, 1191-04-4)
3 alternate names
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tert-Butyl methyl ether
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3 suppliers
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3 alternate names
5 safety hazards
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3 alternate names
2 safety hazards
3 suppliers
DIETHYLENE GLYCOL
(111-46-6)
3 alternate names
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2-HEXANONE
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3 alternate names
3 safety hazards
3 suppliers
NONANOIC ACID
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3 alternate names
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sorbic acid
(110-44-1, 91751-55-2, 22500-92-1)
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(123-92-2)
3 alternate names
3 safety hazards
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(621-64-7)
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(29299-43-2, 110-43-0)
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tert-Amyl methyl ether
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Diisopropyl ether
(108-20-3)
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3 suppliers
N-Nitrosodibutylamine
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thiodiglycol
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(110-97-4, 108-18-9)
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Diacetone alcohol
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(110-44-1)
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6-METHYL-1-HEPTANOL
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2,3-DIMETHYLBUTANE
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2-Ethylhexanal
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