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inquiryProduct Description Product name Diisopropanolamine CAS 110-97-4 Assay 99% Appearance Colorless liquid
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inquiryName Diisopropanolamine Synonyms Bis(2-hydroxypropyl)amine; 1,1'-Iminodi-2-propanol Molecular Structure
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inquiryDiisopropanolamine CAS: 110-97-4 Specification Appearance White powder Content% ≥99.0 pH value (1% in water, 23°C) 10.50-11.50
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Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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inquiryISO Factory/Good qualityAppearance:off white Storage:dry and cool place Package:10G/BAG; 1KG/BAG ;25KG/DRUM Application:Active pharaceutical ingredients Transportation:BY SEA,AIR,EXPRESS Port:SHANGHAI;BEIJING
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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Diisopropanolamine 99%, CAS 110-97-4, High quality DIPA Application:Diisopropanolamine 99%, CAS 110-97-4, High quality DIPA
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
C14H21NO2
A
1-Phenylethanol
B
1-(2-hydroxypropyl)-4-methyl-2-phenylpyrrole
C
diisopropanolamine
Conditions | Yield |
---|---|
With potassium hydroxide Reflux; | A n/a B 33% C n/a |
methyloxirane
diisopropanolamine
Conditions | Yield |
---|---|
With ammonia |
1-(2-imino-5-methyl-oxazolidin-3-yl)-propan-2-ol
diisopropanolamine
Conditions | Yield |
---|---|
With potassium hydroxide In methanol |
Conditions | Yield |
---|---|
In water at 34.4 - 100℃; Thermodynamic data; Equilibrium constant; ΔH,ΔG, ΔS; |
methyloxirane
A
diisopropanolamine
Conditions | Yield |
---|---|
With ammonia; water | |
With ammonia; water |
Conditions | Yield |
---|---|
With potassium hydroxide In water at 80℃; for 2h; Product distribution / selectivity; | |
With potassium hydroxide In water at 80℃; for 2h; Conversion of starting material; Alkaline aqueous solution; |
4,8-dimethyl-2-phenyl-[1,3,6,2]dioxazaborocane
A
diisopropanolamine
B
phenylboronic acid
Conditions | Yield |
---|---|
With water In 1,4-dioxane; water Kinetics; byproducts: (HOCHMeCH2)2NH; hydrolysis in water/dioxane mixts. of different concns.; |
methyloxirane
A
3-amino-2-propanol
B
diisopropanolamine
Conditions | Yield |
---|---|
With ammonia at 41℃; Temperature; Reagent/catalyst; |
methyloxirane
A
triisopropanolamine
B
3-amino-2-propanol
C
diisopropanolamine
Conditions | Yield |
---|---|
With ammonia at 60℃; Temperature; Reagent/catalyst; |
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine; polyparaformaldehyde (degree of polymerization 200) at 85℃; for 3h; Stage #2: With tri-n-propylamine; hydrogen at 45℃; under 11251.1 - 15001.5 Torr; Temperature; Reagent/catalyst; Solvent; | 99.3% |
(6R,7R)-8-Oxo-3-pentafluorophenyloxycarbonyloxymethyl-7-(2-thiophen-2-yl-acetylamino)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
diisopropanolamine
B
(6R,7R)-3-{[Bis-(2-hydroxy-propyl)-carbamoyloxy]-methyl}-8-oxo-7-(2-thiophen-2-yl-acetylamino)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 1h; -26 deg C up to room temp.; Title compound not separated from byproducts; | A n/a B 95% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 24h; | 93% |
diisopropanolamine
bis(iminodiisopropanolato-N,O,O')germanium(IV)
Conditions | Yield |
---|---|
In water refluxing (2 h); cooling, addn. (xylene, EtOH), distillation, solvent redn., crystn. on cooling (0-5°C); elem. anal.; | 92% |
Benzilic acid
diisopropanolamine
(α-hydroxydiphenylaceto-O,O')(iminodiisopropanolato-N,O,O')germanium(IV)
Conditions | Yield |
---|---|
In ethanol; water; xylene refluxing (2 h); solvent removal, crystn. on cooling, filtn., drying (vac.); elem. anal.; | 92% |
1-dodecylbromide
diisopropanolamine
N,N'-bis(2-hydroxypropyl)dodecylamine
Conditions | Yield |
---|---|
In ethanol at 80℃; for 12h; | 90.02% |
hexanedioic acid dimethyl ester
diisopropanolamine
N,N,N',N'-tetrakis(β-hydroxypropyl)adipamide
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine With potassium methanolate at 100℃; for 1h; Green chemistry; Stage #2: hexanedioic acid dimethyl ester for 2h; Reagent/catalyst; Green chemistry; | 89.8% |
With potassium methanolate at 100℃; for 4h; Reagent/catalyst; | 157.3 g |
5-Chloro-2-[2-hydroxy-3-tert-butyl-5-(2-methoxycarbonylethyl)-phenyl]-2H-benzotriazole
diisopropanolamine
Conditions | Yield |
---|---|
With sodium carbonate In cyclohexane at 90℃; for 10h; Inert atmosphere; | 89.7% |
diisopropanolamine
Conditions | Yield |
---|---|
With potassium carbonate In octane at 90℃; for 10h; Solvent; Reagent/catalyst; Inert atmosphere; | 88.1% |
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine With sulfuric acid In water at 178 - 183℃; Stage #2: acetic acid In ethyl acetate at 30℃; Temperature; | 87.2% |
1-Bromotetradecane
diisopropanolamine
N,N'-bis(2-hydroxypropyl)tetradecylamine
Conditions | Yield |
---|---|
In ethanol at 80℃; for 12h; | 87.05% |
diisopropanolamine
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine; 4-bromo-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide In N,N-dimethyl-formamide at 20 - 60℃; for 5h; Stage #2: With sodium hydrogencarbonate In water; N,N-dimethyl-formamide | 87% |
With sodium hydrogencarbonate In N-methyl-acetamide | 240.1 mg (87%) |
diisopropanolamine
2-[2'-hydroxy-3'-tert-butyl-5'-(2''-methoxycarbonylethyl)phenyl]-2H-benzotriazole
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine With sodium acetate In cyclohexane for 2h; Reflux; Stage #2: 2-[2'-hydroxy-3'-tert-butyl-5'-(2''-methoxycarbonylethyl)phenyl]-2H-benzotriazole In cyclohexane at 50℃; for 9h; Reflux; | 85.2% |
Stage #1: diisopropanolamine With sodium acetate In cyclohexane for 2h; Reflux; Stage #2: 2-[2'-hydroxy-3'-tert-butyl-5'-(2''-methoxycarbonylethyl)phenyl]-2H-benzotriazole at 50℃; for 9h; Reflux; | 85.2% |
diisopropanolamine
2,4-Toluene diisocyanate
hyperbranced poly(urea-urethane) copolymer, polycondensation, degree of branching 42.6 percent, Mw 34460; monomer(s): toluene-2,4-diisocyanate; di(2-hydroxypropyl)amine
Conditions | Yield |
---|---|
In N,N-dimethyl acetamide at 80℃; for 120h; | 85% |
di-tert-butyl dicarbonate
diisopropanolamine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 15℃; for 12h; | 83% |
2-(3-chloromethyl-benzoylamino)-5-piperidin-1-yl-benzoic acid ethyl ester
diisopropanolamine
2-(3-{[bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-5-piperidin-1-yl-benzoic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 36h; | 82% |
isophorone diisocyanate
diisopropanolamine
hyperbranched poly(urea-urethane) copolymer, polycondensation, degree of branching 45.8 percent, Mw 28680; monomer(s): isophorone diisocyanate; di(2-hydroxypropyl)amine
Conditions | Yield |
---|---|
In N,N-dimethyl acetamide at 80℃; for 240h; | 81% |
diisopropanolamine
p-toluenesulfonyl chloride
N-tosyl-bis(2-tosyloxy propyl) amine
Conditions | Yield |
---|---|
With hydrogenchloride In pyridine; water | 81% |
diisopropanolamine
di(4-isocyanatophenyl)methane
hyperbranced poly(urea-urethane) copolymer, polycondensation, degree of branching 42.5 percent, Mw 18250; monomer(s): 4,4\-methylenebis(phenyl isocyanate); di(2-hydroxypropyl)amine
Conditions | Yield |
---|---|
In N,N-dimethyl acetamide at 80℃; for 100h; | 79% |
formaldehyd
2-Methoxy-4-methylphenol
diisopropanolamine
C15H25NO4
Conditions | Yield |
---|---|
In methanol for 72h; Mannich condensation; Reflux; | 75% |
diisopropanolamine
Conditions | Yield |
---|---|
at 0℃; | 73% |
diisopropanolamine
Conditions | Yield |
---|---|
With formic acid ethyl ester at 20℃; | 73% |
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine With sulfuric acid In water at 178 - 183℃; Stage #2: propionic acid In ethyl acetate at 45℃; Temperature; | 72% |
Conditions | Yield |
---|---|
Stage #1: diisopropanolamine With sulfuric acid In water at 178 - 183℃; Stage #2: butyric acid In Isopropyl acetate at 45℃; | 71.02% |
diisopropanolamine
Conditions | Yield |
---|---|
at 25℃; | 71% |
diisopropanolamine
bis(pinacol)diborane
Conditions | Yield |
---|---|
In diethyl ether; dichloromethane at 20℃; for 18h; | 71% |
N-[(1S,2R)-1-[[[(1R)-1-1[(3aS,4S,6S,7aR)-hexahydro-3a,5,5-trimethyl-4,6-methano-1,3,2-benzodioxaborol-2-yl]-3-methylbutyl]amino]carbonyl]-2-hydroxypropyl]-6-phenyl-2-pyridinecarboxamide
diisopropanolamine
Conditions | Yield |
---|---|
In tert-butyl methyl ether at 20 - 40℃; for 32h; | 70% |
N-[(1S,2R)-1-[[[(1R)-1-1[(3aS,4S,6S,7aR)-hexahydro-3a,5,5-trimethyl-4,6-methano-1,3,2-benzodioxaborol-2-yl]-3-methylbutyl]amino]carbonyl]-2-hydroxypropyl]-6-phenyl-2-pyridinecarboxamide
diisopropanolamine
Conditions | Yield |
---|---|
In tert-butyl methyl ether at 20 - 40℃; for 32h; | 70% |
4-(trifluoromethoxy)benzonitrile
diisopropanolamine
5-methyl-N-(2-hydroxypropyl)-oxazolidin-2-one
Conditions | Yield |
---|---|
With 3,7-di([1,1′-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine; N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 24h; Reagent/catalyst; Inert atmosphere; Irradiation; Sealed tube; | 70% |
Conditions | Yield |
---|---|
In ethanol at 0℃; for 168h; | 67% |
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