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Toxic Acute

Toxicity. Acute toxicity data for neopentyl glycol (1) are reported in Table 2. [Pg.372]

Toxicity. Acute toxicity data are reported ia Table 2 (11). [Pg.374]

Eastman Chemical Co., BASF, Mitsubishi Gas, and Union Carbide are manufacturers of this glycol. The U.S. price in June 1993 was 2.97/kg. Toxicity. Acute toxicity data for (9) appear in Table 2. [Pg.375]

Sesamex [51-14-9] (Sesoxane) (30) is a synergist oflow toxicity, acute oral LD q (rat) = 2000 2270 mg/kg, for pyrethrins and allethrin. 6,7-Dihydroxy 4-methylcoumarin has been offered as an antioxidant for phenoHcs and polymers, and as an anthelmintic. 2,4,5-Trihydroxybutyrophenone has been available as an antioxidant and light stabilizer for polyolefins, waxes, and foods. Isoflavones, eg (31), have been patented as components of antioxidant compositions for foods and cosmetics (qv) (97). [Pg.381]

Japan. In Japan, registration of dmgs for aquatic species requires the same data as those required for dmgs on other animals. The Ministry of Agriculture, Eorests, and Eisheries and the Ministry of Welfare control the use of chemicals in aquaculture in Japan (17). The preclinical data requirements include product chemistry, toxicity (acute, subacute, special) using rats and mice, safety to target animals, and metaboHsm. The requirements for clinical data include avadabiHty and residues. As of July 1990, more chemicals were registered for aquacultural use in Japan than in any other country (Table 4). [Pg.323]

A toxic reaction may take place during or soon after exposure, or it may only appear after a latency period. Chronic toxicity requires exposure of several years for a toxic effect to occur in humans. With respect to experimental animals, the animals are usually exposed for most or all of their life time to ascertain the occurrence of chronic toxicity. Acute toxic reactions that occur immediately are easy to associate with the exposure and the exposure-effect relationship can readily be demonstrated. The longer the time interval between exposure and effect, the more difficult it is to delineate the relationship between exposure and effect. [Pg.276]

Ascher and Nemny 495) found that residues of triphenyltin acetate on glass, resulting from the evaporation of acetone solutions thereof, were, on contact to houseflies, less toxic with rising concentration. As triphenyltin acetate is likely to be a self-associated polymer in the solid state [similar to trimethyltin acetate (355)] and in concentrated solutions, it was suggested 495) that the monomer, which exists in dilute solutions, is toxic to insects, and the polymer, nontoxic. Interestingly, in this connection, a triphenyltin methacrylate copolymer has 470) a very low mammalian toxicity (acute, oral LDso for mice >2000 mg/kg). [Pg.45]

REDUCED Additional acute toxicity Acute daphnia toxicity Biodegradability Physico-chemical properties 100 kg/annum or 500 kg cumulative... [Pg.458]

Human toxicity Acute effects Carcinogenicity Genotoxicity/mutagenicity Developmental Teratogenicity/mutagenicity Neurotoxicity Endocrine disruption... [Pg.28]

Myelosuppression (dose-related) mucositis (worse with continuous infusion) moderate emetogenic potential alopecia vesicant severe extravasation injury cardiac toxicities acute—not related to cumulative dose arrhythmias, pericarditis chronic— cumulative injury to myocardium (total dose greater than 550 mg/m2 lower total cumulative doses cause damage to myocardium in children (e.g., 350 mg/m2)... [Pg.1408]

In vitro chromosome aberration test In vitro gene mutation assay Acute oral toxicity Acute inhalation or dermal toxicity... [Pg.13]

New compounds continue to appear in the literature and some are reported to show advantages over hydralazine in animal studies. For example, L-6150 (XVI) is said to be less toxic acutely (6). ISF-2123 (XVII) is more potent in rats and dogs (7.). [Pg.58]

Edmiston, C.E., Jr., Goheen, M., Malaney, G.W., and Mills, W.E. Evaluation of carbamate toxicity acute toxicity in a culture of Paramecium multlmlcronucleatum upon exposure to aldicarb, carbaryl, and mexacarbate as measured by a Warburg respirometry and acute plate assay. Environ. Res., 36(2) 338-350, 1985. [Pg.1653]

A toxicity test may measure either acute or chronic toxicity. Acute toxicity is indicative for acute effects possibly occurring in the immediate vicinity of the discharge. An acute toxicity test... [Pg.16]

Acute Oral Toxicity - Acute Toxic Class Method (Updated Guideline, adopted 20 December 2001)... [Pg.20]

Acute oral toxicity - Acute toxic class method 2001... [Pg.109]

Renal toxicity Acute renal failure has been observed in severely ill patients undergoing treatment with voriconazole. [Pg.1677]

Mercury was used to cure the felt used in hats, and workers developed the characteristic signs of mercury vapor toxicity. Acute exposure to high concentrations of mercury vapor causes respiratory distress, which can be fatal. The symptoms of chronic exposure to mercury vapor include personality changes such as excitability, depression, memory loss, fine motor tremor that can become progressively worse, gingivitis, and hallucination. There is some mercury inhalation exposure from dental amalgam, but for most people there are no health-related effects. Metallic mercury is very poorly absorbed from the intestine, thus it is much better to swallow the mercury from a thermometer than inhale it (see chapter on mercury). [Pg.129]

Lead is an acute and a chronic toxicant. Acute effects are ataxia, headache, vomiting, stupor, hallucination, tremors and convulsions. Chronic symptoms from occupational exposure include weight loss, anemia, kidney damage and memory loss. (Patnaik, P. 1999. A Comprehensive Guide to the Hazardous Properties of Chemical Substarwes, 2nbrain damage has been noted among children. Lead bioaccumulates in bones and teeth. The metal is classified as an environmental priority pollutant by the US EPA. [Pg.458]

Thallium chloride is highly toxic. Acute toxic effects are those of thallium poisoning. [Pg.925]

Comprehensive toxicity studies are carried out by animal testing in order to ascertain whether the product exhibits any short-term or long-term toxicity. Acute toxicity is usually assessed by administration of a single high dose of the test drug to rodents. Both rats and mice (male and female) are usually employed. The test material is administered by two means, one of which should represent the proposed therapeutic method of administration. The animals are then monitored for 7-14 days, with all fatalities undergoing extensive post-mortem analysis. [Pg.71]

Phenytoin, like lidocaine, is more effective in the treatment of ventricular than supraventricular arrhythmias. It is particularly effective in treating ventricular arrhythmias associated with digitalis toxicity, acute myocardial infarction, open-heart surgery, anesthesia, cardiac catheterization, cardioversion, and angiographic studies. [Pg.178]

Acute toxicity — acute dose that is lethal in 50% of animals usually two species, usually two routes of administration... [Pg.159]

Ethanol Multiple effects on neurotransmitter receptors, ion channels, and signaling pathways Antidote in methanol and ethylene glycol poisoning Zero-order metabolism duration depends on dose Toxicity Acutely, CNS depression and respiratory failure chronically, damage to many systems, including liver, pancreas, GI tract, and central and peripheral nervous systems Interactions Induces CYP2E1 Increased conversion of acetaminophen to toxic metabolite... [Pg.504]


See other pages where Toxic Acute is mentioned: [Pg.193]    [Pg.130]    [Pg.2273]    [Pg.516]    [Pg.545]    [Pg.607]    [Pg.284]    [Pg.213]    [Pg.123]    [Pg.39]    [Pg.442]    [Pg.109]    [Pg.52]    [Pg.67]    [Pg.44]    [Pg.335]    [Pg.255]    [Pg.340]   
See also in sourсe #XX -- [ Pg.365 ]




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Accidental exposures acute toxicity

Acetylcholinesterase inhibitors acute toxicity

Acute Cd toxicity

Acute Dermal Toxicity

Acute Human Toxicity

Acute Mammalian Toxicity

Acute Toxic Concentration

Acute Toxicants

Acute Toxicants

Acute Toxicity Hazard Level

Acute Toxicity Testing in Drug Safety Evaluation

Acute Toxicity Tests with Aquatic Vertebrates and Macroinvertebrates

Acute Toxicity in Rodents

Acute Toxicity of Benzene

Acute Toxicity of Nitroaromatic Compounds

Acute and Subchronic Toxicity Tests

Acute aquatic toxicity

Acute exposure toxicity

Acute fish toxicity Additive

Acute fish toxicity Additivity

Acute lethality, comparative toxicity

Acute oral toxicity

Acute systemic toxicity

Acute toxic class method

Acute toxicities resistance

Acute toxicity

Acute toxicity

Acute toxicity C12LAS

Acute toxicity Summaries

Acute toxicity additives

Acute toxicity analysis

Acute toxicity animal studies

Acute toxicity anionic surfactants

Acute toxicity anticoagulant rodenticides

Acute toxicity classification

Acute toxicity cyclodienes

Acute toxicity data

Acute toxicity data costs

Acute toxicity data definition

Acute toxicity definition

Acute toxicity determination

Acute toxicity dose-response

Acute toxicity effects

Acute toxicity exposure factors

Acute toxicity focus

Acute toxicity guideline documents

Acute toxicity information sources

Acute toxicity lethal doses

Acute toxicity lethality

Acute toxicity limitations

Acute toxicity measures

Acute toxicity mercury

Acute toxicity of compound

Acute toxicity of cyanide

Acute toxicity of organophosphates

Acute toxicity of pesticides

Acute toxicity of pesticides to honey bees

Acute toxicity organochlorines

Acute toxicity organometallic compounds

Acute toxicity organophosphates

Acute toxicity organophosphorus compounds

Acute toxicity particularly hazardous substances

Acute toxicity pyrethroids

Acute toxicity rating system

Acute toxicity studies

Acute toxicity studies nonrodents

Acute toxicity studies rodents

Acute toxicity systemic effects

Acute toxicity testing purpose

Acute toxicity tests, discussion

Acute toxicity tests, higher animals

Acute toxicity tissues involved

Acute toxicity toxic signs

Acute toxicity tributyltin oxide

Acute toxicity types

Alcohol acute toxic confusion

Antioxidants acute toxicity

Aquatic organisms, acute toxicity

Arsenic compounds acute toxicity

Barbiturates acute toxicity

Behavioral toxicity acute effects

Benzenes acute toxicity

Cadmium acute toxicity

Caffeine acute toxic effects

Carbamazepine acute toxicity

Chlorine acute toxicity

Clinical acute arsenic toxicity

Cyanogen chloride, acute toxicity

Daphnia 48-H acute toxicity test

Earthworm acute toxicity test

Enzyme Activity, Physical Data and Acute Oral Toxicity of Commercial PDS Herbicides

Fish acute toxicity

Fish acute toxicity measures

General Remarks, Acute Toxicity of Benzene

Health hazard classes acute toxicity

Herbicides acute toxicity

Hydrogen cyanide acute lethal inhalation toxicity

Hydrogen cyanide acute toxicity

Hydrogen peroxide acute toxicity

Inhalation toxicity acute

Inhalation toxicity tests, acute

Isoniazid acute toxicity

L, acute toxicity

Lethality, acute toxicity tests

Minimal acute toxicity test

Nonylphenols acute toxicity

Objectives for Assessing the Acute Toxicity of a Substance

Oligonucleotides acute toxicity

Oral toxicity tests, acute

Organophosphates toxicity, acute exposure

Other factors affecting the acute toxicity of pesticides

Pesticides acute toxic symptoms

Pesticides acute toxicity

Poly acute toxicity test

Pyran acute toxicity

Radiation acute toxicity

Rating acute toxicity

Rodent acute toxicity

Safety acute toxicity studies

Sample Acute Toxicity Tests and Commonly Used Species

Selenium compounds, acute toxicity

Studying acute toxicity

Sulfur mustard acute toxic effects

Sulfur mustard acute toxicity

Target site interactions acute toxicity

Testing acute toxicity

The Acute Toxic Properties

Toxaphene acute toxicity

Toxic exposure acute

Toxicity acute lethal

Toxicity tests, acute

Toxicity, acute Reference Dose

Toxicity, acute subacute

Toxicology Acute Toxicity

Using Property Guidelines to Design for Reducing Acute Aquatic Toxicity

Variability, acute toxicity

Vesicants acute toxicity

World health organization acute toxicity

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