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CAS No.: | 10341-25-0 |
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Name: | 1,18-OCTADECANE-DIAMINE |
Article Data: | 7 |
Molecular Structure: | |
Formula: | C18H40N2 |
Molecular Weight: | 284.529 |
Synonyms: | Octadecandiyldiamin;1,18-Octadecanediamine;octadecanediyldiamine;1,18-Diamino-octadecan;octadecanediamine;1,18-diaminooctadecane; |
Density: | 0.854±0.06 g/cm3(Predicted) |
Melting Point: | 93 °C |
Boiling Point: | 365.5±10.0 °C(Predicted) |
PSA: | 52.04000 |
LogP: | 6.54600 |
1,18-octadecanedioic diamide
1,18-octadecane diamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran Reflux; | 98% |
With lithium aluminium tetrahydride In tetrahydrofuran Reflux; | 98% |
With lithium aluminium tetrahydride In tetrahydrofuran Reflux; |
octadecane-1,18-diol
1,18-octadecane diamine
Conditions | Yield |
---|---|
With carbonylchlorohydrido(4,5-bis((diisopropylphosphino)methyl)acridine)ruthenium(II); ammonia In toluene at 150℃; for 65h; Autoclave; Inert atmosphere; | 71% |
1,16-dicyanododecane
1,18-octadecane diamine
Conditions | Yield |
---|---|
With ethanol; sodium | |
With ammonia; hydrogen; nickel In methanol | |
With potassium hydroxide; sodium hydroxide; hydrogen; sponge nickel catalyst In water; hexan-1-ol at 90℃; under 26618.1 Torr; for 2.7h; Product distribution / selectivity; |
1,16-dichloro-hexadecane
1,18-octadecane diamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dimethylformamide 2: H2, NH3 / Raney-Ni / methanol View Scheme |
1,1,1,9-tetrachloro-nonane
1,18-octadecane diamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: HNO3, NO2 2: Na / methanol / (electrolysis) 3: dimethylformamide 4: H2, NH3 / Raney-Ni / methanol View Scheme |
9-chlorononanoic acid
1,18-octadecane diamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: Na / methanol / (electrolysis) 2: dimethylformamide 3: H2, NH3 / Raney-Ni / methanol View Scheme |
octadecanedioic acid
1,18-octadecane diamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: oxalyl dichloride / chloroform / 2 h / 20 °C 2: ammonium hydroxide / tetrahydrofuran / 2 h / 0 - 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / Reflux View Scheme | |
Multi-step reaction with 3 steps 1: chloroform / 2 h / 20 °C 2: ammonia / tetrahydrofuran / 2 h / 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / Reflux View Scheme | |
Multi-step reaction with 2 steps 1.1: 1,1'-carbonyldiimidazole / acetonitrile / 20 °C 1.2: 0 °C 2.1: lithium aluminium tetrahydride / tetrahydrofuran / Reflux View Scheme |
1,18-octadecanedioyl dichloride
1,18-octadecane diamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ammonia / tetrahydrofuran / 2 h / 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / Reflux View Scheme |
octadecane-1,18-diol
A
azacyclononadecane
B
1,18-octadecane diamine
C
1,16-dicyanododecane
Conditions | Yield |
---|---|
With carbonylchlorohydrido(4,5-bis((diisopropylphosphino)methyl)acridine)ruthenium(II); ammonia In toluene at 150℃; for 64h; Autoclave; Inert atmosphere; |
Conditions | Yield |
---|---|
With carbonylchlorohydrido(4,5-bis((diisopropylphosphino)methyl)acridine)ruthenium(II); ammonia In toluene at 150℃; for 64h; Autoclave; Inert atmosphere; |