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Chlorohydrin dinitrates

C1H2C.CH(0.N02).CH2C1 mw 173.99, N 8,0555 col very mobile liq, having an aromatic odor, fr p below -20°, bp 180-90° (dec), d 1.459 at 15° was prepd by nitrating 1,3-dichloro-hydrin with mixed acids (Ref 1). Naoum (Ref 2) reports some addnl props and compares this compd with NG Chlorohydrin Dinitrate (qy) Refs 1) Beil 1, 364 8tU473i 2) Naoum,... [Pg.106]

The most important of the chlorohydrin nitrates are the chlorohydrin dinitrates ( dinitrochlorohydrins ), existing in two isomeric forms ... [Pg.133]

The chemical stability of dinitrochlorohydrin is higher than that of nitroglycerine. It withstands the Abel heat test at 72°C for 30 min. On heating at a temperature of 75°C, the first signs of decomposition and the development of acid fumes do not appear before 10-12 days. A small quantity of chlorohydrin dinitrate heated in a test tube undergoes decomposition with the evolution of oxides of nitrogen at temperature above 170°C. Complete decomposition takes place (without explosion at 180°C. Larger quantities of the substance decompose with a weak explosion, if heated rapidly to a temperature of about 190°C. [Pg.134]

The explosive strength of dinitrochlorohydrin is assumed to be about 80% that of nitroglycerine. As a component of mining explosives chlorohydrin dinitrate has the disadvantage of producing hydrogen chloride on explosion. It does not seem to be any more of practical use. [Pg.135]

In practice, usually a mixture of chlorohydrin with 10-20% of glycerine is nitrated, to yield 165-175 parts of chlorohydrin dinitrates with nitroglycerine. [Pg.136]

Inorganic acid esters nitrates (e.g. methyl nitrate, nitroglycol, nitroglycerine), silicates (e.g. ethyl silicate), phosphates (e.g. triphenyl phosphate, tricresyl phosphate), mixed esters of nitric and hydrochloric acid (e.g. chlorohydrin dinitrate). [Pg.258]

Ethanol amine dinitrate Ethyl chlorothioformate Ethylene chlorohydrin... [Pg.327]

Glycerol (or Glycerin) Chlorohydrin and Its Nitrated Derivatives. See under Chioropropanediol and Derivatives in Vol 3, pp C265-L to C267-L. The dinicrate is described in Blatt, OSRD 2014(1944) as Glycerol Monochlorohy-drin Dinitrate or a-Dinitrochlorohydrin... [Pg.736]

Glcetol Monochlorohydrin Dinitrate or o-Dinitro-chlorohydrin LBCT 83 1.54 TT 135-53... [Pg.276]

Chloropropane l,3 diol l,2 dinitrate or /3-Dinitrochlorohydrin, (02N0).CH2.CHCI.CH2-(ONOz) yel liq, fr p l6.2°(Ref 5,p 173 Ref 6, p 185) can be prepd in a fairly pure state by the action of PC1S on a chlf soln of K-dinitro-chloroglycerin(Ref 6,p 181). It is one of the components of Commercial Dinitrochlorohydrin Commercial Dinitrochlorohydrin is a mixt of a-isomer with a small amt of /S-isomer yellowish to red-bm oil, bp 190°(dec) 121.5° at 13 mm can be prepd by nitrating with HN03-H2S04 commercial chlorohydrin. Its soly other props are almost the same as those of the a-isomer (Refs 5, 6 9)... [Pg.48]

Glycerol dinitrate ( Dinitroglyccrine") Explosive properties Manufacture of dinilroglyccrine Mixed Glycerine Esters Chlorohydrine nitrates... [Pg.343]


See other pages where Chlorohydrin dinitrates is mentioned: [Pg.135]    [Pg.220]    [Pg.400]    [Pg.122]    [Pg.135]    [Pg.237]    [Pg.135]    [Pg.220]    [Pg.400]    [Pg.122]    [Pg.135]    [Pg.237]    [Pg.970]    [Pg.548]    [Pg.465]    [Pg.733]    [Pg.49]    [Pg.465]    [Pg.548]    [Pg.465]    [Pg.971]    [Pg.465]    [Pg.49]    [Pg.548]    [Pg.465]   
See also in sourсe #XX -- [ Pg.133 ]

See also in sourсe #XX -- [ Pg.133 ]




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