Conditions | Yield |
---|---|
With potassium hydroxide; sodium hydroxide; hydrogen; Ni-MC502 In water at 90℃; under 5932.2 Torr; | 99.98% |
With ethanol; sodium | |
With sodium-potassium alloy; butan-1-ol |
α-(dimethylamino)-propionitrile
A
propylamine
B
N,N,N'N'-tetramethyl-1,3-propanediamine
C
1-amino-3-(dimethylamino)propane
D
N,N-bis-(3-dimethylaminopropyl)amine
Conditions | Yield |
---|---|
With caustic; hydrogen; nickel catalyst Degussa MC502 In water at 90℃; under 5932.2 Torr; for 0.45h; Product distribution / selectivity; | A n/a B n/a C 99.98% D n/a |
3-aminopropyl hydrogen sulfate
dimethyl amine
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
With water at 170℃; |
N,N-dimethyl-N-(3-phthalimidopropyl)amine
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
With hydrazine | |
With diazene In ethanol for 3h; |
N,N-Dimethylisobutenylamin
C5H14N2*H(1+)
B
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
ICR double resonance, proton affinity; |
ammonia
3-dimethylaminopropiononitrile
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
at 90 - 100℃; under 66195.7 - 73550.8 Torr; Hydrogenation; |
3-dimethylaminopropiononitrile
butan-1-ol
1-amino-3-(dimethylamino)propane
3-dimethylaminopropiononitrile
butan-1-ol
A
1-amino-3-(dimethylamino)propane
B
N,N-bis-(3-dimethylaminopropyl)amine
A
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
In tetrahydrofuran Equilibrium constant; |
methanol
Trimethylenediamine
A
1-amino-3-(dimethylamino)propane
B
1,3-bis(methylamino)propane
C
N-Methyl-1,3-propanediamine
Conditions | Yield |
---|---|
With Cs-P-Si at 300℃; under 61504.9 Torr; |
Conditions | Yield |
---|---|
Stage #1: dimethyl amine; acrylonitrile for 48h; Stage #2: With sodium In ethanol |
α-(dimethylamino)-propionitrile
A
1-amino-3-(dimethylamino)propane
B
N,N-bis-(3-dimethylaminopropyl)amine
Conditions | Yield |
---|---|
With sodium hydroxide; hydrogen; nickel catalyst Degussa MC502 In water at 90℃; under 5688.78 Torr; Product distribution / selectivity; | |
With lithium hydroxide; hydrogen; nickel catalyst Degussa MC502 In water at 90℃; under 25858.1 Torr; Product distribution / selectivity; | |
With potassium hydroxide; hydrogen; nickel catalyst Degussa MC502 In water at 90℃; under 5171.62 Torr; Product distribution / selectivity; |
Conditions | Yield |
---|---|
Stage #1: dimethyl amine; acrolein at 4℃; for 1.25h; autoclave; Stage #2: With ammonia; hydrogen; Raney cobalt In water at 100℃; under 45004.5 Torr; for 2h; Product distribution / selectivity; autoclave; | 91.4 %Chromat. |
Stage #1: dimethyl amine; acrolein at 4℃; for 1.25h; Stage #2: With ammonia; hydrogen; Ra-Co In water at 100℃; under 45004.5 Torr; for 3h; Autoclave; |
dimethyl amine
acrolein
A
3-Dimethylamino-1-propanol
B
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
Stage #1: dimethyl amine; acrolein at 4℃; for 1.25h; autoclave; Stage #2: With ammonia; hydrogen; Raney cobalt In water at 80℃; under 45004.5 Torr; for 2h; Product distribution / selectivity; autoclave; | A 13.9 %Chromat. B 80.3 %Chromat. |
Stage #1: dimethyl amine; acrolein at 4℃; for 1.25h; Autoclave; Stage #2: With ammonia; hydrogen; Ra-Co In tetrahydrofuran; water at 40℃; under 45004.5 Torr; for 2h; Product distribution / selectivity; Autoclave; | |
Stage #1: dimethyl amine; acrolein at 4℃; for 1.25h; Autoclave; Stage #2: With ammonia; hydrogen; Ra-Co In tetrahydrofuran; water at 40℃; under 45004.5 Torr; for 3h; Product distribution / selectivity; Autoclave; |
N-[3-(dimethylamino)propyl]acrylamide
A
1-amino-3-(dimethylamino)propane
B
acrylic acid
Conditions | Yield |
---|---|
With Rhodococcus erythropolis TA37 acylamidase at 37℃; for 0.333333h; pH=7.5; Kinetics; aq. buffer; Enzymatic reaction; |
hexan-1-amine
A
N-hexyl-1-(4-methoxyphenyl)methanimine
B
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
In [D3]acetonitrile at 24.84℃; Equilibrium constant; |
Conditions | Yield |
---|---|
With hydrogen In ammonia at 80℃; under 18751.9 Torr; Temperature; Pressure; Autoclave; liquid NH3; |
Conditions | Yield |
---|---|
In methanol at 65℃; for 24h; | 100% |
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 100% |
In benzene Heating; | |
In benzene Reflux; Dean-Stark; |
4-nitrobenzaldehdye
1-amino-3-(dimethylamino)propane
N-(4-nitrobenzylidene)-N',N'-dimethyl-1,3-propanediamine
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; |
benzaldehyde
1-amino-3-(dimethylamino)propane
3-(benzylideneamino)-N,N-dimethylpropan-1-amine
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; | |
In methanol at 20℃; Inert atmosphere; | |
In benzene Reflux; Dean-Stark; |
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; |
5-nitro-2-(trichloroacetyl)-1-methylpyrrole
1-amino-3-(dimethylamino)propane
1-Methyl-5-nitro-1H-pyrrole-2-carboxylic acid (3-dimethylamino-propyl)-amide
Conditions | Yield |
---|---|
100% |
2,2,2-trichloro-1-(1-methyl-4-nitro-1H-imidazol-2-yl)ethan-1-one
1-amino-3-(dimethylamino)propane
N-[3-(dimethylamino)propyl]-1-methyl-4-nitroimidazole-2-carboxamide
Conditions | Yield |
---|---|
100% | |
In tetrahydrofuran at 20℃; for 2h; Condensation; | 98% |
In tetrahydrofuran | 90% |
2,2,2-Trichloro-1-(1-methyl-5-nitro-1H-imidazol-2-yl)-ethanone
1-amino-3-(dimethylamino)propane
1-Methyl-5-nitro-1H-imidazole-2-carboxylic acid (3-dimethylamino-propyl)-amide
Conditions | Yield |
---|---|
100% |
4,4-dipropyl-1-carboxycyclohexane-1-acetic acid anhydride
1-amino-3-(dimethylamino)propane
2-<3-(dimethylamino)propyl>-8,8-dipropyl-2-azaspiro<4.5>decane-1,3-dione
Conditions | Yield |
---|---|
Heating; | 100% |
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; |
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In benzene Heating; |
1-amino-3-(dimethylamino)propane
oxalic acid diethyl ester
N,N'-bis(3-dimethylaminopropyl)oxalamide
Conditions | Yield |
---|---|
In ethanol Inert atmosphere; Flow reactor; | 100% |
In tetrahydrofuran at 65℃; for 24h; | 90% |
11-chloro-10H-indolo-[3,2-b]quinoline
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
for 24h; Heating; | 100% |
With phenol at 120℃; for 4h; |
1-amino-3-(dimethylamino)propane
2-chlorobenzo[h]quinoline-3-carboxaldehyde
Conditions | Yield |
---|---|
In ethanol for 4h; Condensation; Heating; | 100% |
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 18h; Condensation; | 100% |
2-chloro-benzaldehyde
1-amino-3-(dimethylamino)propane
N-(2-chlorobenzylidene)-N',N'-dimethyl-1,3-propanediamine
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In chloroform Heating; |
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 18h; | 100% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 18h; | 100% |
With triethylamine In dichloromethane at 23℃; for 1h; | 97% |
1-amino-3-(dimethylamino)propane
1,5,10-trimethoxy-1H-benzo[g]isochromene-3-carbaldehyde
1,5,10-trimethoxy-1H-benzo[g]isochromene-3-carboxylic acid (3-dimethylaminopropyl)-amide
Conditions | Yield |
---|---|
With manganese(IV) oxide; sodium cyanide In isopropyl alcohol at 0℃; for 5h; | 100% |
Conditions | Yield |
---|---|
With sodium carbonate In ethanol for 72h; | 100% |
In methanol |
3,4-dimethoxy-benzaldehyde
1-amino-3-(dimethylamino)propane
N1-(3,4-dimethoxybenzylidene)-N3,N3-dimethylpropan-1,3-diamine
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
In ethanol for 6h; Reflux; |
4,5-dichloro-2-fluoro-phenylamine
1-amino-3-(dimethylamino)propane
4,5-dichloro-N-(3-dimethylaminopropyl)-benzene-1,2-diamine
Conditions | Yield |
---|---|
100% |
Conditions | Yield |
---|---|
With pentafluorophenyl diphenyl-phosphinate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 100% |
perfluorododecanoic acid methyl ester
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
In methanol at 65℃; for 24h; | 100% |
Conditions | Yield |
---|---|
Stage #1: oxirane; ricinus oil; 1-amino-3-(dimethylamino)propane With sodium tetrahydroborate; sodium methylate In methanol at 130℃; for 2h; Stage #2: dimethyl sulfate at 65℃; for 4h; | 100% |
ethyl 7-(4-fluorophenyl)-4-oxo-4H-thieno[3,4-c]pyran-6-carboxylate
1-amino-3-(dimethylamino)propane
ethyl 3-(4-((3-(dimethylamino)propyl)carbamoyl)-3-thienyl)-3-(4-fluorophenyl)-2-hydroxyacrylate
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 2h; | 100% |
2-hydroxy-3-bromobenzaldehyde
1-amino-3-(dimethylamino)propane
2-bromo-6-[(3-dimethylaminopropylimino)methyl]phenol
Conditions | Yield |
---|---|
In methanol at 20℃; for 1h; | 100% |
In methanol at 20℃; | 79% |
N,N-diethyl-4-fluoro-3-nitrobenzamide
1-amino-3-(dimethylamino)propane
Conditions | Yield |
---|---|
Stage #1: 1-amino-3-(dimethylamino)propane With triethylamine In ethanol for 0.5h; Stage #2: N,N-diethyl-4-fluoro-3-nitrobenzamide In ethanol at 50 - 75℃; for 18h; | 100% |
With triethylamine In ethanol at 50℃; | 99% |
Conditions | Yield |
---|---|
Stage #1: C14H13N3O3 With triethylamine In acetonitrile at 20℃; for 0.0833333h; Stage #2: With bis(pentafluorophenyl)carbonate In acetonitrile at 20℃; for 0.75h; Stage #3: 1-amino-3-(dimethylamino)propane With triethylamine In acetonitrile at 20℃; for 18h; | 100% |
furfural
1-amino-3-(dimethylamino)propane
N1-(furan-2-ylmethylene)-N3,N3-dimethylpropan-1,3-diamine
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; Darkness; | 100% |
for 20h; |
Molecular Structure of 3-Dimethylaminopropylamine (CAS NO.109-55-7):
IUPAC Name: N,N-dimethylpropane-1,3-diamine
Empirical Formula: C5H14N2
Molecular Weight: 102.1781
H bond acceptors: 2
H bond donors: 1
Freely Rotating Bonds: 3
Polar Surface Area: 6.48 Å2
Index of Refraction: 1.425
Molar Refractivity: 32.52 cm3
Molar Volume: 127.1 cm3
Surface Tension: 25.1 dyne/cm
Density: 0.803 g/cm3
Flash Point: 9.1 °C
Enthalpy of Vaporization: 34.66 kJ/mol
Boiling Point: 107.8 °C at 760 mmHg
Vapour Pressure: 26.7 mmHg at 25°C
Melting point: -60 °C
storage temp: Flammables area
Water Solubility: Soluble
FreezingPoint: -70°C
BRN: 605293
EINECS: 203-680-9
InChI
InChI=1/C5H14N2/c1-7(2)5-3-4-6/h3-6H2,1-2H3
Smiles
C(N(C)C)CCN
Classification Code: Skin / Eye Irritant
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rabbit | LD50 | skin | 600uL/kg (0.6mL/kg) | Union Carbide Data Sheet. Vol. 12/15/1971, | |
rat | LD50 | oral | 1870mg/kg (1870mg/kg) | American Industrial Hygiene Association Journal. Vol. 23, Pg. 95, 1962. |
Hazard Codes: C
Risk Statements: 10-22-34-43
R10:Flammable.
R22:Harmful if swallowed.
R34:Causes burns.
R43:May cause sensitization by skin contact.
Safety Statements: 26-36/37/39-45
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: UN 2733 3/PG 3
WGK Germany: 2
RTECS: T7525000
HazardClass: 8
PackingGroup: II
HS Code: 29212900
3-Dimethylaminopropylamine , with CAS number of 109-55-7, can be called 1,3-Propanediamine,N,N-dimethyl- (6CI,8CI,9CI) ; (3-Aminopropyl)dimethylamine ; (3-Dimethylaminopropan-1-yl)amine ; 3-(Dimethylamino)propylamine ; N,N-Dimethyl-3-aminopropylamine ; N,N-Dimethyl-N-(3-aminopropyl)amine ; N',N'-Dimethylpropane-1,3-diamine ; g-Dimethylaminopropylamine . It is a clear liquid, 3-Dimethylaminopropylamine (CAS NO.109-55-7) is incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
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