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Trichlorocyanuric acid

Pyrolysis approaches can also be used to prepare substituted isocyanates which caimot be prepared using other methods. For example, A[,A[(A[ -trichlorocyanuric acid [87-90-1] thermally dissociates to yield chloroisocyanate [13858-09-8] and carbonyl diisocyanate [6498-10-8]. The carbonyl isocyanate is unstable and polymerizes (8,94). Table 3 Hsts specialty isocyanates. [Pg.456]

ISOCYANURIC CHLORIDE KYSELINA TRICHLOISOKYANUROVA (CZECH) NSC-405124 SYMCLOSEN SYMCLOSENE TRICHLORINATED ISOCYANURIC ACID TRICHLOROCYANURIC ACID TRICHLOROISOCYANIC ACID TRICHLOROISOCY-ANURIC ACID U,5-TRICHLOROISOCYANURIC ACID... [Pg.1370]

TRICHLOROCHROMIUM see CMJ250 TRICHLOROCYANIDINE see TJD750 TRICHLOROCYANURIC ACID seeTIQ750 TRICHLORO-3-CYCLOHEXENYLSILANE see CPE500... [Pg.1918]

A continuous or semi-continuous process for bleaching of jute fabric with chlorinated derivatives of cyanuric acid is developed [126]. The process comprises a preliminary treatment with boiling water, followed by impregnation of the materials with 0.4-0.6% aqueous alkaline solution, and then subjection of the material to steam treatment. Thereafter, the material is treated at 20-50 C with a mixture of trichlorocyanuric acid and cyanuric acid (with available chlorine content 7-15 g/1), containing sodium carbonate or bicarbonate. The pH of the solution is finally adjusted to 4-5 with acetic acid or phosphoric acid. The treated material is then bleached with H,0,. The time of treatment is usually 40-60 min, but can be extended to 2 h in the case of a heavy fabric with high lignin content. [Pg.200]

For (n = 3) NCS or 2,4,4,6-tetrabromo-2,5-cyclohexadien-l-one (TABCO) or trichlorocyanuric acid, DMSO, CHCI3,4-70min, 87-98% yield. Other thioac-etals are similarly cleaved. ... [Pg.487]

Disinfectant Usually hypochlorite-generating compound (e.g., trichlorocyanuric acid) 0-2... [Pg.563]

TRICHLOROCYANURIC ACID (87-90-1) A powerful oxidizer. Violent reaction with reducing agents. Reacts with acrolein, antimony trisulfide, antimony tritelluride, arsenic pentasulfide, 1,1-dichloro-l-nitroethane, 1,3-dichloropropene, diethylamine, s-trioxane. Incompatible with -bis(trichlormethyl)benzene. Reacts with nitrogen-containing com-pounds ammonia, amines, urea, forming the unstable explosive nitrogen trichloride. Contact with combustible material, organic substances may cause fire. [Pg.1171]

Trlchloro-5-((4-chlorophenyl) sulfonyl) benzene. See Tetradifon Trichlorochromium. See Chromium chloride (ic) Trichlorocyanidine. See Cyanuric chloride Trichloro-3-cyanopropylsilane. See 3-Cyanopropyltrichlorosilane Trichlorocyanuric acid. See Trichloroisocyanuric acid Trichlorodecylsilane. Seen-Decyltrichlorosilane... [Pg.4487]

Synonyms Isocyanuric chloride TCCA 1,3,5-Triazine-2,4,6(1H,3H,5H), 1,3,5-trichloro- Trichlor Trichlorinated isocyanuric acid Trichlorocyanuric acid Trichloroisocyanic acid 1,3,5-Trichloroisocyanuric acid N,N, N"-Trichloroisocyanuric acid 1,3,5-Trichloro-... [Pg.4490]

For aromatic chlorination with TiCl4 and CF3COO2H see Tetr Lett (1970) 2611 " " trichlorocyanuric acid see joc (1970) 35 719... [Pg.350]

The second protein modifying group of reagents we sought are based on monomethoxy-polyethylene glycol (M-PEG). Polyethylene glycol has been attached to proteins by using sy/n-trichlorocyanuric acid and by conver-... [Pg.296]

Trichlorocyanuric acid has been reported to be an effective laboratory chlorinating reagent for nuclear or side-chain halogenation of aromatic systems. [Pg.44]

See other pages where Trichlorocyanuric acid is mentioned: [Pg.1012]    [Pg.991]    [Pg.563]    [Pg.218]    [Pg.1026]    [Pg.814]    [Pg.877]    [Pg.1048]    [Pg.13]    [Pg.308]    [Pg.1012]    [Pg.991]    [Pg.563]    [Pg.218]    [Pg.1026]    [Pg.814]    [Pg.877]    [Pg.1048]    [Pg.13]    [Pg.308]   
See also in sourсe #XX -- [ Pg.266 ]



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