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Iso-propyl nitrate

The mechanisms of n- and iso-propyl nitrate decomposition flames appear to be the same as that of the ethyl nitrate flame, the main attack on the nitrate ester being by nitrogen dioxide and nitrous acid [136]. [Pg.489]

For iso-propyl nitrate the main products acetaldehyde and CH3NO2 are formed in the following sequence... [Pg.489]

More recent work has shown that, below about 200 °C, the pyrolysis of iso-propyl nitrate follows first-order kinetics. The main products are... [Pg.489]

Gray and co-workers [120] examined the decomposition of iso-propyl nitrate at elevated temperatures... [Pg.165]

Nitrooxypropane [2-propyl nitrate, iso-propyl nitrate, CH3CH(0N02)CH3] ... [Pg.1535]

C3H7N03 PROPYL-NITRATE -177.035 4.9531 E-01 1.9599E-05 -27.32 171 C4H10O METHYL-ISO- -254.443 4.3538E-01 3.8072E-05 -120.88... [Pg.378]

Di(2>nitroxy-iso-propyl)>amine Nitrate N,N-Di(jS nitroxy-iso-propyl)-amine Nitrate or N,N-Bis(/8-nitroxy-iso-propyl)-amine Nitrate,... [Pg.392]

Di (propyl)-amine and derivs 5 D1498—D1499 di (2-nitroxy-iso-propyl)-amine nitrate 5 D1498 di (2-nitroxy-iso-propyl)-nitramine 5 D1498 N,N-di (3-nitroxypropyl)-nitramine 5 D1499... [Pg.585]

In our attempts to synthesize nano structured or even nanoporous chromium (III) oxide we used a great variety of surfactants (amines, polyethylen oxides, carboxylates, sulfates, phosphates and quartemary alkylammonium salts) and Cr3+ precursors (nitrate, acetate, acetylacetonate and iso-propyl ate) to obtain the desired materials [19]. Different kinds of interaction are established throughout the structure-directing process such as electrostatic (S+... [Pg.363]

As previously pointed out a practical application has been found for isopropyl nitrate. It was originally bebeved 111") that the substance could only be made from iso-propyl iodide and silver nitrate. Direct nitration was found to yield mainly acetone due to the oxidation of the secondary alcoholic group. However a process of continuous nitration of iso-propyl alcohol in the presence of urea has been described by Imperial Chemical Industries patents [36]. isopropyl alcohol and urea were introduced into nitric acid (over 40% HNOj) at its boiling temperature and a current of air stirred and removed unstable products. According to Desscigne (118) the method gave ca. S0% yield. He used nitric acid of over 50% HNO3 at 108-1 lO C. [Pg.165]

DIAZINON or DIAZINONE (333-41-5) A weak base. Hydrolyzes slowly in water and dilute acid. With excess water, this compound produces diethylthiophosphoric acid and 2-iso-propyl-4-methyl-6-pyrimidol. With insufficient water, this compound produces highly toxic tetraethyl monothiopyrophosphate. Incompatible with antimony(V) pentafluoride, diacetate, magnesium, silver nitrate. Reacts with strong acids, alkalis, copper-containing compounds, oxidizers. [Pg.389]

See other pages where Iso-propyl nitrate is mentioned: [Pg.157]    [Pg.165]    [Pg.165]    [Pg.358]    [Pg.343]    [Pg.351]    [Pg.157]    [Pg.165]    [Pg.165]    [Pg.165]    [Pg.358]    [Pg.234]    [Pg.157]    [Pg.165]    [Pg.165]    [Pg.358]    [Pg.343]    [Pg.351]    [Pg.157]    [Pg.165]    [Pg.165]    [Pg.165]    [Pg.358]    [Pg.234]    [Pg.956]    [Pg.957]    [Pg.123]    [Pg.130]    [Pg.5]    [Pg.579]    [Pg.373]    [Pg.420]    [Pg.260]    [Pg.123]    [Pg.957]    [Pg.958]    [Pg.420]    [Pg.165]    [Pg.48]    [Pg.387]   
See also in sourсe #XX -- [ Pg.343 , Pg.351 ]



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3- propyl nitrate

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