Acetates toxicity

There is no specific treatment for vinyl acetate toxicity. Supportive and symptomatic treatment is recommended. 

Effect. Monitoring of hematological parameters may be useful as a biomarker of effect of 2-butoxyethanol and 2-butoxyethanol acetate. Toxic effects occur in the red blood cells and are either from 2-butoxyethanol or its metabolites (Bartnik et al. 1987 Ghanayem et al. 1987a, 1987b). However, hematological effects are not specific to 2-butoxyethanol. The tests cannot be relied upon to find... 

Rice DC (1989) Brain and tissue levels of mercury after chronic methyl mercury exposure in the monkey. ] Toxicol Environ Health 27 189-198. Roberts MC, Seawright AA and Ng JC (1979) Chronic phenylmercuric acetate toxicity in a horse. Vet Hum Toxicol 21 321-32. 

Kostial K, Maljkovic T, Jugo S (1974) Lead acetate toxicity in rats in relation to age and sex. Arch Toxikol 31 265-269... 

Extracts of sweet maijoram have antioxidant/ free radical scavenging properties that are in part due to labiatic, ursolic and camosic acids, and camosol and phenolic compounds. The antioxidant activity is reflected in the ability of the volatile oil and different maijoram extracts to act as liver and kidney chemopreventive agents against lead acetate toxicity in mice. ... 

In Equation 6.1, P, r, and p refer to plasmid DNA/cell, intrinsic synthesis rate, and specific growth rate, respectively. Thus, when temperature is increased, de novo synthesis in terms of increases several fold while p-driven cytoplasmic dilution decreases somewhat. The combination results in a significantly increased rate of plasmid DNA accumulation per cell. Overall, reduced kinetics during the cell propagation phase is traded off against lessened acetate toxicity and metabolic burden. 

CH2CI2. A colourless liquid with a chloroform-like odour b.p. 4I°C. Prepared by heating chloroform with zinc, alcohol and hydrochloric acid manufactured by the direct chlorination of methane. Decomposed by water at 200°C to give methanoic and hydrochloric acids. Largely used as a solvent for polar and non-polar substances, particularly for paint removal (30%), dissolving cellulose acetate and degreasing (10%). It is more stable than carbon tetrachloride or chloroform especially towards moisture or alkali. It is somewhat toxic. U.S. production 1981 280000 tonnes. 

C10H10N4O2S. White powder, which darkens on exposure to light m.p. 255-256 C. Prepared by condensing p-acet-amidobenzenesulphonyl chloride with 2-aminopyrimidine and subsequent hydrolysis. Soluble sulphadiazine is the sodium salt. Sulphadiazine is the least toxic of the more potent sulphonamides. ... 

Acrolein is a highly toxic material with extreme lacrimatory properties. At room temperature acrolein is a Hquid with volatiUty and flammabiUty somewhat similar to acetone but unlike acetone, its solubiUty in water is limited. Commercially, acrolein is always stored with hydroquinone and acetic acid as inhibitors. Special care in handling is required because of the flammabiUty, reactivity, and toxicity of acrolein. 

CeUulose triacetate is insoluble in acetone, and other solvent systems are used for dry extmsion, such as chlorinated hydrocarbons (eg, methylene chloride), methyl acetate, acetic acid, dimethylformamide, and dimethyl sulfoxide. Methylene chloride containing 5—15% methanol or ethanol is most often employed. Concerns with the oral toxicity of methylene chloride have led to the recent termination of the only triacetate fiber preparation faciHty in the United States, although manufacture stiH exists elsewhere in the world (49). 

Emulsives are solutions of toxicant in water-immiscible organic solvents, commonly at 15 ndash 50%, with a few percent of surface-active agent to promote emulsification, wetting, and spreading. The choice of solvent is predicated upon solvency, safety to plants and animals, volatility, flammabiUty, compatibihty, odor, and cost. The most commonly used solvents are kerosene, xylenes and related petroleum fractions, methyl isobutyl ketone, and amyl acetate. Water emulsion sprays from such emulsive concentrates are widely used in plant protection and for household insect control. 

The LC q (lowest possible lethal concentration) has been reported to be 23 ppm for a 30 min exposure time (mouse), 53 ppm for an exposure time of 100 min (rat, rabbit, and guinea pig), and 200 ppm for an exposure time of 10 min (monkey). No toxic effects were reported upon exposure to 1 ppm for 7 h/d over 55 days. The oral LD q (rat) of ketene is 1300 mg/kg, the low level of toxicity probably being due to the almost immediate formation of acetic acid and other acetates in the digestive tract. 

Another level of regulatory significance is the toxic characteristic leach procedure (TCLP) limit of a characteristic waste. A material which is a waste because of the TCLP is ha2ardous if a Hquor resulting from an 18-h leach in an acetic acid buffer exceeds 5 ppm (mg/L) lead in the leach Hquor. 

Reactions. Heating an aqueous solution of malonic acid above 70°C results in its decomposition to acetic acid and carbon dioxide. Malonic acid is a useful tool for synthesizing a-unsaturated carboxyUc acids because of its abiUty to undergo decarboxylation and condensation with aldehydes or ketones at the methylene group. Cinnamic acids are formed from the reaction of malonic acid and benzaldehyde derivatives (1). If aUphatic aldehydes are used acryhc acids result (2). Similarly this facile decarboxylation combined with the condensation with an activated double bond yields a-substituted acetic acid derivatives. For example, 4-thiazohdine acetic acids (2) are readily prepared from 2,5-dihydro-l,3-thiazoles (3). A further feature of malonic acid is that it does not form an anhydride when heated with phosphorous pentoxide [1314-56-3] but rather carbon suboxide [504-64-3] [0=C=C=0], a toxic gas that reacts with water to reform malonic acid. 

Prior to the 1990s phenyhnercuric acetate was the primary bactericide and fungicide in latex and waterborne paints. Because of the increasing concerns of mercury toxicity and the potential for high consumer and occupational exposures to mercury when present in paints, the U.S. Environmental Protection Agency (EPA) induced U.S. manufacturers of PMA and other mercury compounds to withdraw their registrations for use of these substances as biocides in paints (see AIercury). Mercury compounds are used only for very limited, specific purposes, such as the use of phenyhnercuric mXx.2LX.e[55-68-5] as a bactericide in cosmetic eye preparations (see Cosmetics). 

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