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Silver picrate

Silver Picrate (also called Pikratol in Ger). C H2(N02)3 0Ag mw 335.98 N 12.51% fine yel needles mp, 315° with decompn bp, expld ca 335°, or when brought in contact with an open flame was not ignited or detonated by the spit of a fuse when compressed in a detonator cap. Can be prepd by dissolving Ag oxide in a hot satd PA soln (Ref 3)... [Pg.759]

Although the transport of dry lead picrate is forbidden by the Department of Transportation (DOT) (49 CFR 172.101), the addition of water desensitizes it. No hazard classification is available from DOT for wetted lead picrate, but silver picrate, which is similar in sensitivity, may not be shipped when dry but is classified as a flammable solid (Hazard Class/Division 4.1) when it is wetted with water by at least 30 percent by mass. [Pg.52]

Colgan ST, Krull IS, Dorschel C, et al. 1986. Derivatization of ethylene dibromide with silica-supported silver picrate for improved high-performance liquid chromatographic detection. Anal Chem 58 2366-2372. [Pg.115]

Several silver compounds are extremely explosive—for example, silver picrate, silver nitride, silver peroxide, silver perchlorate, and silver permanganate. They are used in various types of explosives and as concussion caps for rifle and pistol ammunition. [Pg.143]

Silver picrate, wetted with not less than 30 per cent water, by mass 1347... [Pg.145]

Trinitroanisol may also be prepared by the interaction of methyl iodide and silver picrate, and by the nitration of anisic acid, during which the carboxyl group is lost, but the most convenient method appears to be that of Jackson70 and his collaborators by which a methoxy group is substituted for chlorine in a nucleus already nitrated. A methyl alcohol solution of picryl... [Pg.170]

SYNS PICRAGOL PICROTOL SILVER PICRATE (dry) (DOT) SILVER PICRATE, wetted with not <30% water, bv weight (UN1347) (DOT)... [Pg.1128]

Derivation Interaction of methyl iodide and silver picrate, nitration of anisic acid. [Pg.1284]

Alkylation of polyhydric phenols such as resorcinol, hydroxyhydroquinone, orcinol, and pyrogallol with an alkyl iodide and alkali gives nuclear alkylation products as well as aryl ethers.760 In this reaction phioroglucinol gives hexa-methyl-l,3,5-cyclohexanetrione but there is a 65% yield of the 0-alkylation product 1,3,5-trimethoxybenzene if the mixture is kept acid during the alkylation.761 Philbrook and Massey762 report the preparation of picryl ethers from silver picrate and alkyl halides. [Pg.365]

Triazolium or substituted triazolium picrates were first prepared via direct reaction of the triazole with picric acid in methanol or with silver picrate after... [Pg.71]

Silver-silver picrate Also see other entries... [Pg.196]

Silver-silver perchlorate EMF 834 Silver-silver picrate EMF 194-197, 834 Silver salicylate SI 66... [Pg.924]

Heterogeneous derivatizations, either in thepre- or postcolumn mode, using a reagent as a solid or bonded to packing particles have been explored by Krull and co-workers. Alkyl iodides and epoxides were converted to picryl ethers using silica supported silver picrate before HPLC separation. UV detectability at 220 nm was markedly improved with detection limits at the ppb level. Lower detectability was possible using either reductive or photolysis electrochemical detection. [Pg.233]


See other pages where Silver picrate is mentioned: [Pg.476]    [Pg.118]    [Pg.347]    [Pg.330]    [Pg.476]    [Pg.337]    [Pg.104]    [Pg.106]    [Pg.340]    [Pg.440]    [Pg.293]    [Pg.118]    [Pg.835]    [Pg.838]    [Pg.858]    [Pg.244]    [Pg.330]    [Pg.293]    [Pg.1127]    [Pg.1349]    [Pg.5708]    [Pg.118]    [Pg.738]    [Pg.751]    [Pg.340]   
See also in sourсe #XX -- [ Pg.118 ]

See also in sourсe #XX -- [ Pg.170 ]

See also in sourсe #XX -- [ Pg.170 ]

See also in sourсe #XX -- [ Pg.118 ]




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