Phenyl mercury acetate

Phenyl Carbylamine Chloride Phenyl Dibromoarsine Phenyl Dichloroarsine Phenyl Mercury Acetate Phenylaceyl Chloride Phenylarsenic Dichloride Phenylarsonous Dichloride Phenylcarbamine Phenylcarbonimidic Dichloride Phenylchloromethylketone Phenylisocyanide Dichloride Phenylisonitrile Dichloride Phenylmethylaminpropane Philippine Downy Mildew Phix... 

Acetic acid dodine, fentin, glyodin, phenyl mercury acetate, see acetyl chloride chloro acetic acid... 

Mercuric acetate methoxy ethyl mercury acetate, phenyl mercury acetate... 

PHENOMERCURIC ACETATE PHENYLMERCURI-ACETATE PHENYL MERCURIC ACETATE PHENYL-MERCURY ACETATE PHENYLQUECK-SILBERACETAT (GERMAN) PHIX PMA PMAC PMACETATE PMAL PMAS PURASAN-SC-10 PURATURF 10 QUICKSAN RCRA WASTE NUMBER P092 SANITIZED SPG SC-110 SCUTL ... 

Dimethylaminophenyl4-Flnorophenyl Tellurium Dichloride In a 250 ml flask fitted with a reflux condenser are placed 16.5 g (50 mmol) of 4-fluorophenyl tellurium trichloride, 19.0 g (50 mmol) of 4-dimcthylamino-phenyl mercury acetate, and 100 ml of absolute dioxane. The mixture is heated under reflux for 8 h during which time it acquires a dark violet color. The mixture is allowed to cool to 20", the precipitated mercury(II) chloride/dioxane adduct is filtered off, and activated charcoal is added to the filtrate which is then heated under reflux for 30 min. The mixture is allowed to cool and is then passed through a layer of aluminum oxide. The filtrate is concentrated to one-fourth of its original volume by distillation, the concentrate is diluted with 100 ml of hexane to precipitate the product which is filtered off, washed with hexane, dried, and recrystallized from propanol yield 7.2 g (35%) m.p. 145°. 

Phenyl mercury acetate Fungicide, unclassified herbicide... 

CAS 123-88-6 Agent Index A156 Phenyl Mercury Acetate CAS 62-38-4... 

The role of siroheme in the reduction of nitrite is supported by the observation that nitrite perturbs the spectrum of the oxidized or reduced enzyme. Carbon monoxide reaction with the reduced siroheme can be followed spec-trophotometrically. The complex can be dissociated with oxygen. The kinetics of CO-complex formation and dissociation correspond with those for CO inhibition of nitrite reductase. The inhibition of nitrite reductase by p-chloromercuribenzoate, phenyl mercury acetate, and sodium mersalyl demonstrate the involvement of SH groups presumably associated with cysteine residues found in nitrite reductase. Epr studies and spectral data indicate the oxidation/reduction of iron sulfur centers and the formation of a NO-heme complex however, other intermediates have not been confirmed (Aparicio et al., 1975 Vega and Kamin, 1977 Hucklesby et al., 1979). 

Phthalic acid phenols, removal Hydrogen peroxide phenyl mercury acetate mfg. 

Product COSAN JTA-20 is a highly functional, soluble, phenyl-mercury acetate which has been deposited on an inert, synthetic, hydrous calcium silicate to produce a free-flowing, relatively non-dusting powder which is simple to incorporate into dry formulations. COSAN JTA-20 contains 20% phenylmercury acetate as the active ingredient equivalent to 12% mercury expressed as metal. 

Phenyl Mercury Acetate Mercury metal content Appearance ... 

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