| Identification | Back Directory | [Name]
N,N-Diamylnitrosamine | [CAS]
13256-06-9 | [Synonyms]
NSC 7360
NSC 73601
Diamylnitrosamin
Diamylnitrosamine
NITROSODIAMYLAMINE
Dipentylnitrosamine
N-Nitrosodiamylamine
Di-N-amylnitrosamine
Dipentylnitrosoamine
N,N-Diamylnitrosamine
N-Nitrosodipentylamine
Di-N-pentylnitrosamine
N-Nitrosodi-N-amylamine
Dipentylamine, N-nitroso-
N,N-dipentylnitrous amide
N-NITROSODI-N-PENTYLAMINE
N-NITROSO-N-PENTYL-1-PENTAMINE
N-Nitroso-N-pentyl-1-pentanamine
1-Pentanamine, N-nitroso-N-pentyl- | [Molecular Formula]
C10H22N2O | [MOL File]
13256-06-9.mol |
| Chemical Properties | Back Directory | [Appearance]
colourless to light yellow liquid | [Boiling point ]
320.8°C (rough estimate) | [density ]
0.9698 (rough estimate) | [refractive index ]
1.4710 (estimate) | [storage temp. ]
Refrigerator | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [CAS DataBase Reference]
13256-06-9 |
| Hazard Information | Back Directory | [Chemical Properties]
colourless to light yellow liquid | [General Description]
Clear light yellow liquid. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
A nitrated amine. Amines are combustible. The combustion of amines yields noxious NOx. REACTIVITY - Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups. |
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