Glycol Monophenyl Ether Research Articles

Assessment of ethylene glycol monobutyl and monophenyl ether reproductive toxicity using a continuous breeding protocol in Swiss CD-1 mice

A continuous breeding reproduction study design was utilized to examine the reproductive toxicity of ethylene glycol monobutyl ether (EGBE) and ethylene glycol monophenyl ether (EGPE). Swiss CD-1 mice were administered EGBE in drinking water (0, 0.5, 1.0, and 2.0%, i.e., 0.7, 1.3, and 2.1 g/kg body wt/day) and EGPE was administered via the feed (0, 0.25, 1.25, and 2.5%, i.e., 0, 0.4, 2.0, and 4 g/kg body wt/day). Both male and female mice were dosed for 7 days prior to and during a 98-day cohabitation period. EGBE was toxic at the high (2%) and mid dose (1%) to adult F 0 female mice: 13 out of 22 females at the high dose and 6 out of 20 at the mid dose died during the cohabitation period. Both the high- and mid-dose animals produced fewer litters/pair, fewer pups/litter, with decreased pup weight. These effects occurred in the presence of decreased body weight, decreased water consumption, and increased kidney weight. A crossover mating trial indicated that the reproductive effects could be attributed primarily to an effect on the female. This was substantiated at necropsy where testes and epididymis weights were normal as were sperm number and motility. Fertility of the offspring of the 0.5% group was normal in the presence of increased liver weights. With respect to EGPE, there was no change in the ability to produce five litters during the continuous breeding period. There was, however, a significant but small (10–15%) decrease in the number of pups/litter and in pup weight in the high-dose group. A crossover mating trial suggested a female component of the reproductive toxicity of EGPE. While fertility was only minimally compromised, severe neonatal toxicity was observed. By Day 21 there were only 8 out of 40 litters in the mid- and high-dose groups which had at least one male and female/litter. Second generation reproductive performance of the mid-dose group (1.25%) was unaffected except for a small decrease in live pup weight. In summary the reproductive toxicity of EGBE and EGPE was only evident in the female and occurred at doses which elicited general toxicity. EGBE was particularly toxic to adult female mice while EGPE was particularly toxic to immature mice of both sexes.

Assessment of Ethylene Glycol Monobutyl and Monophenyl Ether Reproductive Toxicity Using a Continuous Breeding Protocol in Swiss CD-1 Mice

Assessment of Ethylene Glycol Monobutyl and Monophenyl Ether Reproductive Toxicity Using a Continuous Breeding Protocol in Swiss CD-1 Mice. HEINDEL, J. J., GULATI, D. K., RUSSELL, V. S., REEL, J. R., LAWTON, A. D., AND LAMB, J. C., IV. (1990). Fundam. Appl Toxicol. 15,683–696. A continuous breeding reproduction study design was utilized to examine the reproductive toxicity of ethylene glycol monobutyl ether (EGBE) and ethylene glycol monophenyl ether (EGPE). Swiss CD-1 mice were administered EGBE in drinking water (0, 0.5, 1.0, and 2.0%, i.e., 0.7, 1.3, and 2.1 g/kg body wt/day) and EGPE was administered via the feed (0, 0.25, 1.25, and 2.5%, i.e., 0,0.4,2.0, and 4 g/kg body wt/day). Both male and female mice were dosed for 7 days prior to and during a 98-day cohabitation period. EGBE was toxic at the high (2%) and mid dose (1%) to adult F0 female mice: 13 out of 22 females at the high dose and 6 out of 20 at the mid dose died during the cohabitation period. Both the high- and mid-dose animals produced fewer litters/pair, fewer pups/litter, with decreased pup weight. These effects occurred in the presence of decreased body weight, decreased water consumption, and increased kidney weight. A crossover mating trial indicated that the reproductive effects could be attributed primarily to an effect on the female. This was substantiated at necropsy where testes and epididymis weights were normal as were sperm number and motility. Fertility of the offspring of the 0.5% group was normal in the presence of increased liver weights. With respect to EGPE, there was no change in the ability to produce five litters during the continuous breeding period. There was, however, a significant but small (10–15%) decrease in the number of pups/litter and in pup weight in the high-dose group. A crossover mating trial suggested a female component of the reproductive toxicity of EGPE. While fertility was only minimally compromised, severe neonatal toxicity was observed. By Day 21 there were only 8 out of 40 litters in the mid- and high-dose groups which had at least one male and female/litter. Second generation reproductive performance of the mid-dose group (1.25%) was unaffected except for a small decrease in live pup weight. In summary the reproductive toxicity of EGBE and EGPE was only evident in the female and occurred at doses which elicited general toxicity. EGBE was particularly toxic to adult female mice while EGPE was particularly toxic to immature mice of both sexes.

Mass transfer of acetylacetone, ethylene glycol mono- n-butyl ether and ethylene glycol monophenyl ether across water-carbon tetrachloride and water-chloroform interfaces

The interfacial mass transfer kinetics of acetylacetone (acac), ethylene glycol mono- n-butyl ether (EGBE) and ethylene glycol monophenyl ether (EGPE) across water-carbon tetrachloride (Ccl 4) and water-chloroform (CHCl 3) interfaces were studied by stirring the two phases at various speeds, maintaining a quiescent interface with a constant area. In the analysis of data, two rate-determining steps consisting of a diffusion toward the interface and a mass exchange between the interface and bulk phases are considered. It is shown that the transfer of EGBE and EGPE in both CHCl 3 and Ccl 4 systems is controlled by the diffusion step even at high stirring speeds, whereas the transfer of acac in Ccl 4 is controlled by the interfacial exchange step at high stirring speeds. An irreversible transfer has been also observed in the EGBE and EGPE systems at low stirring speeds.

Experimental Studies on Toxicity of Ethylene Glycol Alkyl Ethers in Japan

Past studies on the toxicological effects of ethylene glycol alkyl ethers as well as the recent data on these chemicals in Japan are reviewed. Only a few researchers have participated in the study of ethylene glycol alkyl ethers in Japan. The effects of ethylene glycol alkyl ethers on testis and embryotoxic effects of ethylene glycol monomethyl ether (EGM) have been studied, as has the teratogenicity of ethylene glycol dimethyl ether (EGdM). Studies on ethylene glycol alkyl ethers and related compounds administered to mice by oral gavage revealed the occurrence of testicular atrophy and decreased white blood cell count by EGM, EGdM, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether and ethylene glycol monoethyl ether acetate, and the toxicity was related to their chemical structure. On the other hand, ethylene glycol, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, ethylene glycol monophenyl ether, ethylene glycol monoacetate or ethylene glycol diacetate showed no such an effect. Studies on EGM using hamsters or guinea pigs revealed the occurrence of testicular atrophy similar to that observed in mice. In regard to the methyl ethers of other glycols, there is no convincing evidence that propylene glycol monomethyl ether, diethylene glycol monomethyl ether or diethylene glycol dimethyl ether causes testicular atrophy in mice. Teratological studies of EGM and EGdM revealed embryotoxic effects in mice.

Experimental studies on toxicity of ethylene glycol alkyl ethers in Japan.

Past studies on the toxicological effects of ethylene glycol alkyl ethers as well as the recent data on these chemicals in Japan are reviewed. Only a few researchers have participated in the study of ethylene glycol alkyl ethers in Japan. The effects of ethylene glycol alkyl ethers on testis and embryotoxic effects of ethylene glycol monomethyl ether (EGM) have been studied, as has the teratogenicity of ethylene glycol dimethyl ether (EGdM). Studies on ethylene glycol alkyl ethers and related compounds administered to mice by oral gavage revealed the occurrence of testicular atrophy and decreased white blood cell count by EGM, EGdM, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether and ethylene glycol monoethyl ether acetate, and the toxicity was related to their chemical structure. On the other hand, ethylene glycol, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, ethylene glycol monophenyl ether, ethylene glycol monoacetate or ethylene glycol diacetate showed no such an effect. Studies on EGM using hamsters or guinea pigs revealed the occurrence of testicular atrophy similar to that observed in mice. In regard to the methyl ethers of other glycols, there is no convincing evidence that propylene glycol monomethyl ether, diethylene glycol monomethyl ether or diethylene glycol dimethyl ether causes testicular atrophy in mice. Teratological studies of EGM and EGdM revealed embryotoxic effects in mice.

Testicular atrophy of mice induced by ethylene glycol mono alkyl ethers (author's transl)

Toxicities of ethylene glycol (EG) and 6 ethylene glycol mono alkyl ethers administered orally were studied. Mice were given various doses (62.5, 125, 250, 500, 1,000, 2,000 and 4,000 mg/kg body weight) of the compounds daily for 5 days/week, for 5 weeks. High doses of ethylene glycol mono methyl ether (EGM), ethylene glycol mono methyl ether acetate (EGMA), ethylene glycol mono ethyl ether (EGE) and ethylene glycol mono ethyl acetate (EGEA) produced marked testicular atrophy and leucopenia. Dose-responce relation was found in these effects. EGM was more effective than EGE, while ethylene glycol mono butyl ether and ethylene glycol mono phenyl ether had but slight effect and EG had no detectable action on testis and leucocytes. Toxic doses being expressed as mg/kg body weight, esterification seemed to weaken the atrophic action of EGM and EGE, but when expressed as mol/kg, significant difference was found neither between EGM and EGMA nor between EGE and EGEA. The mechanism of testicular atrophy induced by low ethylene glycol mono alkyl ethers is likely to be an inhibitory action on cell division.

A one-solution triacid general stain which differentiates oxygenated from nonoxygenate red blood corpuscles.

Tissues from representative mammals, amphibia and invertebrates were fixed for 5-24 hr in either an aqueous solution of 8% p-toluene sulfonic acid (PTSA) or in 10% formalin to which 5 gm PTSA/100 ml had been added, and processed through embedding in polyethylene glycol 400 distearate in the usual manner. Sections cut at 4-6 μ were floated on 0.2% gelatin containing 1.25% formalin, and spread and dried on slides at a temperature not exceeding 25 C. Wax was removed with xylene, and the sections brought to water through ethanol as usual. The working staining solution was made from three stock solutions: A. Chlorantine fast blue 2RLL, 0.5%; B. Cibacron turquoise blue G-E, 0.5%; C. Procion red M-P, 0.5%—each of which was dissolved in 98.5 ml of distilled water to which 0.5 ml of glacial acetic acid and 0.5 ml of propylene glycol monophenyl ether (a fungicide) had been added. For use, the three solutions were mixed in the proportions: A, 3; B, 4; and C, 3 volumes. Staining time was uncritical, 10-30 min usually sufficing for 6 μ, sections. The chief feature of the staining is the differentiation of oxygenated and nonoxygenated red blood corpuscles, in reds and blues respectively. Connective tissue stained blue or blue-green and mucin, green. Nuclei and cytoplasm stain according to their condition at the time of fixation. The mixed stain keeps well, remaining active after 2 yr of storage.

Über Steroide. 109. Mitteilung. Papierchromatographie von schwach polaren Steroiden

AbstractA critical survey of the known methods of paper chromatography of steroids is given. A new solvent system is described which, in connection with several colour reactions, is particularly applicable to the separation, identification and purity analysis of weakly polar steroids or corresponding esters and ethers. The stationary phase is formed by ethyleneglycol monophenylether (phenylcellosolve) on Whatman paper No. 7, the mobile phase by heptane or a similar non‐polar solvent.

Use of repellents in clinical dermatology; general principles.

AMONG the advances in preventive medicine in the last world war were the detailed studies in the chemical control of insects. As yet, the practicing physician, as compared with the military physician, does not appear to be fully aware of the possibilities for the control of insects, especially the disease-bearing types. This chemical control, in general, falls into two phases: insecticidal and repellent activity. The development of insecticides is well known from the advances in the preparations of pyrethrins and DDT (2,2-bis [p-chlorophenyl]-1,1,1-trichloroethane) and its newer analogues, such as DDD (1,1-dichloro-2,2-bis-[p-chlorophenyl]-ethane) and methoxychlor (1,1,1trichloro-2,2-bis [p-methoxyphenyl]-ethane. Perhaps less is known about the developments of new insecticidal materials, which include such substances as gammexane® (hexachlorocyclohexane), velsicol 1068® (also called chlordan), hexaethyltetraphosphate, piperine compounds, parathion (0,0-diethyl-0-p-nitrophenyl thiophosphate), very toxic, phenyl cellosolve® (ethylene glycol monophenyl ether) and eura® (10 per cent crotonyl-N-ethyl-ortho-toluidide). 1 Dermatologists should be interested also in the