• 제목/요약/키워드: bromobenzene

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Toxicological Studies on the Essential Oil of Eugenia caryophyllata Buds

  • Park, Hee-Juhn
    • Natural Product Sciences
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    • 제12권2호
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    • pp.94-100
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    • 2006
  • The essential oil (EC-oil) obtained from the buds of Eugenia caryophyllata (Myrtaceae) was examined for its free radical-scavenging activity, cytotoxicity, and in vivo toxicity. To find the xenobiotic properties of EC-oil, serum thiobarbituric acid reactive substances (TBARS) level and hepatic drug-metabolizing enzyme activities were measured. It was found that EC-oil displayed xenobiotic properties like bromobenzene. The cytotoxicities of eugenol and of the EC-oil were greatly attenuated by the sulfhydryl-containing N-acetyl-L-cysteine (NAC), suggesting that eugenol was susceptible to nucleophilic sulfhydryl. In addition, eugenol also showed potent free radical-scavenging activity in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Moreover, methyleugenol considerably exhibited less cytotoxicity and less potent free radical-scavenging activity than eugenol, and the cell viability of the methyleugenol was more increased with NAC treatment than the eugenol. These results indicate that the phenolic OH in eugenol may play a crucial role in both cytotoxicity and free radical-scavenging activity. The fashion on oxidative stress and hepatic drug-metabolizing enzyme activities of eugenol resembled those of bromobenznene.

저근백피(樗根白皮) 성분(成分)의 생리생활(生理生活)에 관한 연구(硏究)(I) -메탄올 추출물과 클로로포름 분획이 Epoxide 분해계에 미치는 영향- (Studies on the Biologic Activities of the Constituents of Ailanthi Cortex Radicis(I) -Effects of Methanol Extract and its Chloroform Fraction on Epoxide Hydrolyzing System in Liver-)

  • 김종;최종원;김혜경;박수완;이정규
    • 생약학회지
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    • 제25권1호
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    • pp.47-50
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    • 1994
  • For the biological survey, effects of Ailanthi Cortex Radicis, the root bark of Ailanthus altissima(Simaroubaceae) on epoxide hydrolyzing enzymes were checked. The methanolic extract and its chloroform fraction were shown to activate the liver metabolizing enzyme system including epoxide hydrolase system which was monitored by activities of transaminase, lactate dehydrogenase, alkaline phosphatase and epoxide hydrolase system in bromobenzene treated rats. But they showed no effect on glutathione S-transferase activity.

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Carbonylation of 1-Bromo-2,6-bis(bromomethyl)benzene Catalyzed by Cobalt Carbonyl

  • Sang Chul Shim;Shin Ae Chae;Dong Yeob Lee;Young Zoo Youn;Jae Goo Shim;Chil Hoon Doh
    • Bulletin of the Korean Chemical Society
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    • 제14권4호
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    • pp.481-485
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    • 1993
  • Dialkyl 1-bromobenzene-2,6-diacetates were easily prepared by the carbonylation of the moiety of benzylic bromide in 1-bromo-2,6-bis(bromomethyl)benzene with alcohol in the presence of NaOAc< TEX>${\cdot}$3H$_2$O and a catalytic amount of Co$_2$(CO)$_8$under the atmospheric pressure of carbon monoxide at room temperature in excellent yield. Alkyl 2,6-bis(alkoxymethyl)benzoates were obtained by the carbonylation of the moiety of aryl bromide in 1-bromo-2,6-bis(alkoxymethyl)-benzene, which derived from 1-bromo-2,6-bis(bromomethyl)benzene, alcohol, NaOR, and CH$_3$I under the same conditions. Alkyl 2,6-bis(carboxymethyl)benzoate was also obtained in a trace amount for 24 hrs at room temperature.

The Photochemical Reactivities of Benzenes Tethered to Haloarene

  • 박용태;김영희;황철균;성대동
    • Bulletin of the Korean Chemical Society
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    • 제17권6호
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    • pp.506-510
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    • 1996
  • The syntheses and photoreactions of haloarenes, in which the aryl and haloaryl moieties are tethered by a simple alkyl group, were studied. For 2-benzyl-1-halobenzene, in which two aryl moieties were connected by methylene group, photoreduced product, diphenylmethane, was obtained along with the minor formation of the photocyclized product, fluorene, in acetonitrile solvent. For 1-halo-2-phenethylbenzene, in which two aryl moieties were connected by ethylene group, photocyclized products, 9,10-dihydrophenanthrene and phenanthrene, were obtained along with the minor formation of photoreduced product, bibenzyl, in acetonitrile solvent. The photoreaction selectivities in several solvent systems were studied: In cyclohexane, 2-benzyl-1-chlorobenzene was photoreduced more effective than 2-benzyl-1-bromobenzene; In the presence of NaOH, 1-halo-2-phenethylbenzenes gave 9,10-dihydrophenanthrene and, in the presence of toluene, they gave phenanthrene. A radical reaction mechanism is proposed for the explanation of the reactions. This study shows that the photoreaction of haloarene, in which haloaryl and aryl moieties are tethered by ethylene group, can be used for ring formation of 9,10-dihydrophenanthrene otherwise difficultly accessible.

Reactions of Aryl Organometallic Reagents with Isomers of Phthalonitriles: Triaryl Diketimines and Diketones

  • Lee, Woo-Young;Kim, Young-Soo;Sim, Won-Bo;Park, Chang-Hee;Ahn, Yoon-Mo;Park, Oee-Sook
    • Bulletin of the Korean Chemical Society
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    • 제7권5호
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    • pp.362-366
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    • 1986
  • Synthesis and hydrolysis of aromatic diketimines of triaryl type were investigated by the action of aryl organometallics on the three isomers of phthalonitrile. The reactions of organometallic reagents, prepared from bromobenzene, o-bromotoluene and o-bromoanisol, with iso- and terephthalonitrile proceeded in normal way. Decomposition of the addition complex with dry ammonia, methanol or water gave six diketimines, which could be hydrolysed to the corresponding diketones. Reactions of phthalonitrile with the organometallic reagent were different from the other isomers, so that the decomposition and hydrolysis of the addition complex did not give diimines and the corresponding aromatic diketones.

업종별 산업폐수의 수질오염물질 배출 특성 (A Study on the Characteristic Trace of Water Quality Pollutants in the Industrial Wastewater)

  • 박선구;김성수;고오석
    • 분석과학
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    • 제12권2호
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    • pp.141-150
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    • 1999
  • 영산강 수계 광주천, 황룡강, 지석천, 영산강 상류 유역내에 분포된 9개 업종 76개 배출원의 원폐수 및 방류수로부터 20개 유기화학물질 tetrachloroethylene, toluene, ethylbenzene, p-xylene, m-xylene, isopropyl benzene, stylene, bromobenzene, 1,3,5-trimethylbenzene, 2-chlorotoluene 1,2,4-trimethylbenzene, p-isopropyltoluene, 4-chlorotoluene, n-butylbenzene, 1,2,4-trichlorobenzene, naphthalene, tert-butylbenzene, sec-butylbenzene, phenol, isopropyl benzene hydroperoxide를 액체-액체 추출법으로 분리하여 기체 크로마토그래피/질량 분석계(GC/MS)로 분석하였고, 포준품과 비교함으로써 밝혔다. 특히, 화학업종의 원폐수에는 검출되지 않았으나 방류수에는 폐놀과 이소프로필벤젠 하이드로퍼옥사이드가 검출되었다. 중금속 Cr, Mn, Cu, Zn, Cd, Pb, As, Al, Fe은 모든 업종의 원폐수에 대부분 함유되어 있었으며, 이중 Fe와 Al은 다른 중금속에 비행 원폐수에 다소 많이 검출되었다. Cr, Cd, Pb, As은 전기전자, 금속업종의 원폐수에서 다소 많은 양이 함유되었으며, 이러한 9개 중금속들은 폐수처리과정에서 거의 처리가 되어 방류수에는 환경 기준 이하로 검출되거나 불검출되었다.

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GIS 기법을 활용한 서울시 VOCs 오염도평가에 관한 연구 (Assessment of the VOCs Concentration Using GIS Method of Seoul)

  • 박기학;정용;조성준
    • 환경영향평가
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    • 제10권2호
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    • pp.135-145
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    • 2001
  • This study was conducted to investigate the practical using of Geographic Information System(GIS) technology which are computer-based systems that are used to store and manipulate geographic information on the air pollution control and management in the macro city. For this study 130 samples were corrected by passive sampler in Seoul (25 distincts) distributed by TM-coordinate during November in 1997 to January 1998, and analysed by GC/MSD for 16 VOCs e.g., toluene, benzene and display using Arc/view GIS(version 3.2, ESRI Inc, U.S.A) for windows. The most VOCs concentration distribution in November, 1997 was higher than that of January, 1998 except benzene and 1,1,2-trichroloethan, bromobenzene. And products of the distribution of VOCs concentration display using GIS technology was effective as well as other display methods(e.g., contouring method, pie or column chart, graduated symbols), especially in mapping and symbolization capabilities for spatial pollutant status evaluation were very effective than other display methods.

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Potent Antimutagenic and Their Anti-Lipid Peroxidative Effect of Kaikasaponin III and Tectorigenin from the Flower of Puer-aria thunbergiana

  • Park, Kun-Young;Jung, Geun-Ok;Choi, Jong-Won;Lee, Kyung-Tae;Park, Hee-Juhn
    • Archives of Pharmacal Research
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    • 제25권3호
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    • pp.320-324
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    • 2002
  • The MeOH extract of Pueraria thunbergiana (Leguminosae) flowers and its fractions were subjected to Ames test to test the antimutagenicity. EtOAc fraction (1 mg/plate) decreased the number of revertants of Salmonella typhymurium TA100 by 95% against aflatoxin $B_1{\;}(AFB_1)$. Phytochemical isolation of the EtOAc fraction afforded four isoflavonoids (tectorigenin, glycitein, tectoridin and glycitin) and one saponin (kaikasaponin III). Though the three isoflavonoids other than tectoridin showed significant antimutagenicity, the activity of kaikasaponin III was the most potent. Kaikasaponin III (1 mg/plate) decreased the number of revertants of S. typhymurium TA 100 by 99% against $AFB_1$ but by 75% against N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Tectorigenin (1 mg/plate) inhibited the $AFB_1$-induced mutagenicity by 90% and MNNG-induced one by 76%. Glycitein and glycitin were less active than tectorigenin and kaikasaponin III. This result suggested that kaikasponin III prevents the metabolic activation of $AFB_1$ and scavenge electrophilic intermediate capable of mutation. The two components with potent activities, tectorigenin and kaikasaonin III, significantly prevented the malondialdehyde formation caused by bromobenzene in the rat.

카페트에서 방출되는 VOCs의 방출특성 (Emission Characteristics of Volatile Organic Compounds (VOCs) from a Carpet)

  • 신동민;김창녕;김동술
    • 설비공학논문집
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    • 제15권1호
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    • pp.40-49
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    • 2003
  • This study has been conducted to identify and quantify the emissions of Volatile Organic Compounds (VOCs) from a new carpet. The carpet sample consists of polypropylene cushion and latex backing. The VOCs have been sampled on sorbent tubes and analyzed by thermal desorption unit and GC/MSD. For over 240 hours, concentration of VOCs has been measured in a small chamber made of stainless steel. With the measured data, emission factor and mass balance have been considered. The experiments have been conducted in accordance with ASTM D5116-97. The carpet has emitted a variety of VOCs, but in this study, 7 VOCs compounds have been considered: chlorobenzene, ethylbenzene, styrene, isopropylbenzene, bromobenzene, 2-chlorotoluene, and 1,2,3-trimethylbenzene. The results show that the concentrations of VOCs and the emission factors have exponentially decayed from relatively high level to low level with time. The gradients of the concentration of VOCs and emission factors are different for various components. It is found that styrene, 2-chlorotoluene are emitted more than others with higher concentrations.

BSO 유도 루타치온 저감 흰쥐에서 1, 2, 4-trichlorobenzene의 급성독성에 관한 연구 (The Acute Toxicity of 1, 2, 4-Trichlorobenzene in Sprague-Dawley Rats Depleted of Glutathione by Treatment with Buthionine Sulfoximine)

  • 안영수;권명희;이정섭;김정우;김대선;류홍일;강인구
    • Environmental Analysis Health and Toxicology
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    • 제11권1_2호
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    • pp.41-47
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    • 1996
  • 1, 2, 4-Trichlorobenzene (1, 2, 4-TCB) is used as a dye carrier, as an intermediate in the synthesis of herbicides, as a flame retardant, and for other purpose. After a single oral administration of 1, 2, 4-TCB (200 mg/kg, 400 mg/kg) in rats, toxic effects were studied by means of serum biochemical and heatological analysis, and liver calcium concentration. Administration of 1, 2, 4-TCB resulted in dose-dependent liver and kidney damage as estimated by increased serum alanine aminotransferase (ALT) activities, liver calcium concentration and blood urea nitrogen (BUN). Pretreatment with DL-buthionine sulfoximine (BSO, 2 mmol/kg, i.p. ) considerably decreased liver glutathione concentration, which was accompanied by markedly elevated serum ALT activites. It is well-known that toxicity of halogenated benzene such as bromobenzene, 1, 4-dichlorobenzene is increased by pretreatment of henobarbital (PB), and protected by pretreatment of cytochrome P450 inhibitor including metyrapone (MP). However, there was no obvious alterations in toxicity of 1, 2, 4-TCB by pretreatment of phenobarbital or metyrapone. In comparison with control group, treatment groups exhibited significant changes in some parameters of hematological analysis but all hematological values remined within normal ranges.

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