2-(3-bromopropyl)isoindole-1,3-dione
dibutylamine
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With xylene at 140 - 150℃; Kochen des erhaltenen N-<3-Dibutylamino-propyl>-phthalimids mit konz.HCl.; | |
(i) xylene, (ii) aq. HCl; Multistep reaction; |
3-(dibutylamino)propanenitrile
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With ethanol; sodium | |
With nickel at 95℃; under 2206.5 Torr; Hydrogenation; | |
With ethanol; nickel at 70℃; under 2942.03 Torr; Hydrogenation; | |
With lithium aluminium tetrahydride; diethyl ether |
N-(3-dibutylamino-propyl)-phthalimide
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With hydrazine |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: N2H4 View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: Raney nickel; ethanol / 70 °C / 2942.03 Torr / Hydrogenation View Scheme | |
Multi-step reaction with 2 steps 2: Raney nickel / 95 °C / 2206.5 Torr / Hydrogenation View Scheme |
Conditions | Yield |
---|---|
In methanol; water at 65℃; for 0.166667h; Schiff Reaction; Inert atmosphere; | 100% |
In neat (no solvent) at 25℃; for 24h; Kinetics; Solvent; |
3-[8-(2,6-difluorophenyl)-2-(methylsulfinyl)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methyl-N-(1-methylethyl)benzamide
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 96% |
In tetrahydrofuran at 20℃; | 96% |
N-Methylisatoic anhydride
3-dibutylaminopropylamine
N-Methyl-N'-(3-dibutylaminopropyl)anthranilic amide
Conditions | Yield |
---|---|
In 1,4-dioxane at 70℃; for 8h; | 94.5% |
1,3,5-trichloro-2,4,6-triazine
3-dibutylaminopropylamine
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
Stage #1: 1,3,5-trichloro-2,4,6-triazine; N-acetyl-p-phenylenediamine With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 45℃; for 1h; Stage #2: 3-dibutylaminopropylamine With N-ethyl-N,N-diisopropylamine In tetrahydrofuran for 3h; Reflux; Stage #3: With hydrogenchloride; methanol; water for 2.5h; Reflux; | 90% |
1,3,5-trichloro-2,4,6-triazine
3-dibutylaminopropylamine
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
Stage #1: 1,3,5-trichloro-2,4,6-triazine; N-acetyl-p-phenylenediamine With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 45℃; for 1h; Stage #2: 3-dibutylaminopropylamine With N-ethyl-N,N-diisopropylamine In tetrahydrofuran for 3h; Reflux; Stage #3: With hydrogenchloride; methanol; water for 2.5h; Reflux; | 90% |
Conditions | Yield |
---|---|
With samarium(III) nitrate hexahydrate In chloroform at 20℃; for 20h; | 85% |
Conditions | Yield |
---|---|
Stage #1: cholic acid With triethylamine In tetrahydrofuran for 0.166667h; Cooling; Stage #2: With chloroformic acid ethyl ester In tetrahydrofuran at 20℃; for 2.16667h; Cooling; Stage #3: 3-dibutylaminopropylamine In tetrahydrofuran for 3h; | 84% |
3-[8-(2,6-difluorophenyl)-2-(methylsulfinyl)-7-oxo-5,6,7,8-tetrahvdropyrimido[4,5-d]pyrimidin-4-yl]-4-methyl-N-propylbenzamide
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 83% |
In dichloromethane at 20℃; | 83% |
ethyl (3-ethyl-4-methyl-2-oxo-2H-1-benzopyran-7-yloxy)acetate
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In butan-1-ol at 20℃; for 48h; | 83% |
6-iodo-2-phenyl-4Hbenzo[d][1,3]oxazin-4-one
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 82% |
benzo[b]thiophene-3-carbonyl azide
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In benzene Heating; | 80% |
1,4,5,8-naphthalenetetracarboxylic dianhydride
3-dibutylaminopropylamine
N,N'-bis(3-N,N-dibutylaminopropyl)naphthalene-1,8:4,5-bis(dicarboxamide)
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 140℃; for 0.166667h; Microwave irradiation; | 80% |
In toluene for 3h; Substitution; Heating; | 76% |
3-dibutylaminopropylamine
4-butylamino-3-ethoxycyclobut-3-ene-1,2-dione
3-(butylamino)-4-((3-(dibutylamino)propyl)amino)cyclobut-3-ene-1,2-dione
Conditions | Yield |
---|---|
In ethanol at 20℃; for 12h; Inert atmosphere; | 80% |
perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With 1H-imidazole; zinc diacetate at 160℃; for 4h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
In butan-1-ol at 20℃; for 48h; | 79% |
6-bromo-2-phenyl-4H-benzo[2,3-d]-1,3-oxazin-4-one
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 75% |
2-chloro-5-(5-nitrofuran-2-yl)-1,3,4-thiadiazole
3-dibutylaminopropylamine
N-(3-(dibutylamino)propyl)-5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-amine
Conditions | Yield |
---|---|
In ethanol Reflux; | 73% |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 24h; | 72% |
sofalcone
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 24h; | 71% |
Conditions | Yield |
---|---|
Stage #1: 3-dibutylaminopropylamine; 3,4-dichlorobenzaldehyde In methanol at 20℃; for 1h; Stage #2: With methanol; sodium tetrahydroborate for 1h; | 70.4% |
3-dibutylaminopropylamine
camphoric anhydride
(1R,5S)-3-[3-(dibutylamino)propyl]-1,8,8-trimethyl-3-azabicyclo[3.2.1]octane-2,4-dione
Conditions | Yield |
---|---|
In ethanol Reflux; | 70% |
at 180℃; |
formaldehyd
3-dibutylaminopropylamine
1-Di-n-butylamino-3-dimethylamino-propan
Conditions | Yield |
---|---|
With formic acid In water at 80℃; for 24h; | 66.1% |
3-[8-(2,6-difluorophenyl)-2-(methylsulfinyl)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-N-(4-fluorophenyl)-4-methylbenzamide
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 66% |
In tetrahydrofuran at 20℃; | 66% |
10-Chloro-6-methyl-5H-pyrido<3',4':4,5>pyrrolo<2,3-g>isoquinoline
3-dibutylaminopropylamine
N,N-Dibutyl-N'-(6-methyl-5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolin-10-yl)-propane-1,3-diamine
Conditions | Yield |
---|---|
at 160℃; for 5h; | 53% |
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20 - 60℃; | 50% |
Conditions | Yield |
---|---|
In water; acetonitrile at 20℃; for 18h; aminomethylation; Mannich reaction; | 48% |
5'-[(cyclopropylamino)carbonyl]-4-{[(2,2-dimethylpropyl)amino]carbonyl}-3'-fluoro-2'-methyl-2-biphenylcarboxylic acid
3-dibutylaminopropylamine
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide at 20℃; | 48% |
7-chloro-6-(2-chloroethyl)-5-methyl-1,2,4-triazolo<1,5-a>pyrimidine
3-dibutylaminopropylamine
Dibutyl-[3-(5-methyl-6,7-dihydro-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidin-8-yl)-propyl]-amine
Conditions | Yield |
---|---|
With triethylamine In ethanol for 2h; Heating; | 47% |
1,4-Dihydroxynaphthalene
3-dibutylaminopropylamine
2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione
Conditions | Yield |
---|---|
With cerium(III) chloride heptahydrate; triethylamine In ethanol at 20℃; for 6h; | 38% |
With cerium(III) chloride heptahydrate; triethylamine In ethanol at 20℃; for 4h; |
3-dibutylaminopropylamine
[1,4]naphthoquinone
2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione
Conditions | Yield |
---|---|
In ethanol; dichloromethane at 20℃; | 36.1% |
IUPAC Name: N,N-dibutylpropane-1,3-diamine
The MF of N,N-dibutylpropane-1,3-diamine (102-83-0) is C11H26N2.
The MW of N,N-dibutylpropane-1,3-diamine (102-83-0) is 186.34.
Synonyms of N,N-dibutylpropane-1,3-diamine (102-83-0): (3-Aminopropyl)dibutylamine ; 1,3-Propanediamine, N,N-dibutyl- ; 3-(Dibutylamino)propylamine
Product Categories: Pharmaceutical Raw Materials
Form: Clear colourless liquid
Index of Refraction: 1.457
EINECS: 203-059-2
Density: 0.843 g/ml
Flash Point: 103.9 °C
Boiling Point: 205 °C
Melting Point: -50 °C
Water Solubility: 10 G/L (20 ºC)
BRN: 635829
N,N-dibutylpropane-1,3-diamine (102-83-0) is used as organic synthesis intermediates.
1. | skn-rbt 100 µg/24H open | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
2. | orl-rat LD50:820 mg/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
3. | skn-rbt LD50:270 mg/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. |
Reported in EPA TSCA Inventory.
Poison by skin contact. Moderately toxic by ingestion. A skin irritant. Ignites on contact with cellulose nitrate. When heated to decomposition it emits toxic fumes of NOx.
Safety information of N,N-dibutylpropane-1,3-diamine (102-83-0):
Hazard Codes C,Xi
Risk Statements
34 Causes burns
36/37/38 Irritating to eyes, respiratory system and skin
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39 Wear suitable protective clothing, gloves and eye/face protection
45 In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
RIDADR UN 2922 8/PG 3
WGK Germany 3
RTECS TX7175000
HazardClass 8
PackingGroup II
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