Basic information Safety Supplier Related

N,N-Diamylnitrosamine

Basic information Safety Supplier Related

N,N-Diamylnitrosamine Basic information

Product Name:
N,N-Diamylnitrosamine
Synonyms:
  • 1-Pentanamine, N-nitroso-N-pentyl-
  • Diamylnitrosamin
  • Di-N-amylnitrosamine
  • Di-N-pentylnitrosamine
  • Dipentylnitrosoamine
  • N-Nitrosodi-N-amylamine
  • Diamylnitrosamine
  • Dipentylnitrosamine
CAS:
13256-06-9
MF:
C10H22N2O
MW:
186.29
Product Categories:
  • All Aliphatics
  • Aliphatics
  • Nitric Oxide Reagents
Mol File:
13256-06-9.mol
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N,N-Diamylnitrosamine Chemical Properties

Boiling point:
320.8°C (rough estimate)
Density 
0.9698 (rough estimate)
refractive index 
1.4710 (estimate)
storage temp. 
Refrigerator
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Oil
pka
-3.15±0.70(Predicted)
color 
Clear Colourless to Pale Yellow
Stability:
Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference
13256-06-9
EPA Substance Registry System
N,N,-Diamylnitrosamine (13256-06-9)
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N,N-Diamylnitrosamine Usage And Synthesis

Chemical Properties

colourless to light yellow liquid

Uses

N,N-Diamylnitrosamine (cas# 13256-06-9) is a compound useful in organic synthesis.

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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