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| CAS No.: | 110-58-7 |
|---|---|
| Name: | Amylamine |
| Molecular Structure: | |
|
|
|
| Formula: | C5H13N |
| Molecular Weight: | 87.1649 |
| Synonyms: | Pentylamine(8CI);1-Aminopentane;1-Pentylamine;Monoamylamine;Monopentylamine;NSC 7906;Norleucamine;n-Amylamine;n-Pentylamine;1-Pentanamine; |
| EINECS: | 203-780-2 |
| Density: | 0.755 g/cm3 |
| Melting Point: | -55 °C(lit.) |
| Boiling Point: | 105.5 °C at 760 mmHg |
| Flash Point: | 4.4 °C |
| Solubility: | soluble |
| Appearance: | clear colourless to very slightly yellow liquid |
| Hazard Symbols: |
F, C
|
| Risk Codes: | 11-22-34-42/43-20/21/22 |
| Safety: | 16-26-36/37/39-45-33 |
| Transport Information: | UN 1106 3/PG 2 |
| PSA: | 26.02000 |
| LogP: | 1.83560 |

| Conditions | Yield |
|---|---|
| With borane-ammonia complex; C15H30Cl2CoN3P In hexane at 120℃; for 16h; Sealed tube; Inert atmosphere; chemoselective reaction; | 86% |
| With hydrogen; sodium methylate; nickel In methanol hydrogen generated in situ electrochemically on Raney nickel electrode; | 72% |
| With lithium aluminium tetrahydride | 71% |

| Conditions | Yield |
|---|---|
| With ammonia; hydrogen In methanol at 30℃; for 15h; Autoclave; | 94% |
| With ammonium hydroxide; ammonium acetate; hydrogen; [Ru(cod)Cl]2; trisodium tris(3-sulfophenyl)phosphine In toluene at 145℃; under 48754.9 Torr; for 10h; | 47 % Chromat. |
| With ammonium hydroxide; hydrogen at 65℃; under 11251.1 Torr; for 12h; Autoclave; Green chemistry; | |
| With pyridoxal 5'-phosphate; Amine transaminase 117; rac-methylbenzylamine; N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid In water; dimethyl sulfoxide at 30℃; Reagent/catalyst; Enzymatic reaction; |

pentyl azide


1-pentanamine

| Conditions | Yield |
|---|---|
| With hydrogen; MCM-silylamine Pd(II) In methanol at 20℃; for 2h; Reduction; | 90% |

5-chloro-valeric acid

A

piperidine

B

piperidin-2-one

C

1-pentanamine

D

N-butylamine

| Conditions | Yield |
|---|---|
| Stage #1: 5-chloro-valeric acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry; Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6.5h; Cooling with ice; Green chemistry; | A 85% B 9% C 2% D 2% |


| Conditions | Yield |
|---|---|
| With sodium hydroxide; benzyltrimethylazanium tribroman-2-uide In water at 70℃; for 2h; | 80% |
| With sodium hydroxide; sodium bromite In water at 75℃; for 0.5h; | 60% |
| With sodium hypochlorite |

| Conditions | Yield |
|---|---|
| With carbonylchlorohydrido(4,5-bis((diisopropylphosphino)methyl)acridine)ruthenium(II); ammonia; water In 1,4-dioxane at 135℃; under 5700.38 Torr; for 30h; Inert atmosphere; | A 70.0 %Chromat. B n/a |

N,N'-dipentyl-oxalamide


1-pentanamine

| Conditions | Yield |
|---|---|
| With potassium tert-butylate; hydrogen; [Ru(PtBuNNHBn)H(CO)Cl] In toluene at 135℃; under 30003 Torr; for 24h; | 97 %Spectr. |

valeraldoxime


1-pentanamine

| Conditions | Yield |
|---|---|
| With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
| With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
| With palladium on activated charcoal; acetic acid Hydrogenation; |

| Conditions | Yield |
|---|---|
| With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
| With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
| With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |

| Conditions | Yield |
|---|---|
| With sodium hydroxide; sodium persulfate; sodium chloride In water at 85 - 90℃; for 7h; | A 36% B 56% |
| With sodium hydroxide; sodium persulfate; copper dichloride In water at 85 - 90℃; for 7h; | A 36% B 56% |
| With sodium hydroxide; sodium persulfate; sodium chloride In water at 85 - 90℃; for 7h; | A 36% B 52% |
| With sodium hydroxide; sodium persulfate; sodium chloride In water at 85 - 90℃; for 7h; | A 36% B 52% |

| 1. | ipr-rat LDLo:37,500 µg/kg | FATOAO Farmakologiya i Toksikologiya (Moscow). 31 (1968),238. |