• Journal of the Korean Chemical Society
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• v.47 no.6
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• pp.559-568
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• 2003

A procedure based on liquid liquid extraction(LLE)-GC/MS has been developed for the simultaneous analysis of antioxidants and insecticides known as endocrine disrupters. The endocrine disrupters investigated in this study are butylated hydroxy anisole(BHA) and butylated hydroxy toluene(BHT), and the insecticides are allethrin and fenvalerate. The limit of detection(LOD) was 0.071~0.159 ng/ml with RSD of 1.41~5.34% for the standard sample. From water reservior of Han river, Geum river, Nakdong river and Sumjin river, these compounds were not detected. For the synthesized sample, the LOD is 0.051~0.132 ng/ml with RSD of 6.39~13.4%.

• Applied Biological Chemistry
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• v.38 no.5
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• pp.414-421
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• 1995

In order to establish informations important to the measurement of lipoxygenase (LOX) activity, providing conditions most favorable for its action and determining factors that inhibit activity, the influence of extraction buffer, substrate, pH, storage, temperature, NaCl, $CaCl_2$, other cations and antioxidants on LOX activity, and localization of LOX in cucumber tissues were carried out. The most favored substrate for LOX was linolenic acid followed by linoleic and arachidonic acids. LOX activity in both peel and mesocarp tissue extracts was maximum at pH 5.5 and relatively stable at $40^{\circ}C\;and\;50^{\circ}C$ temperature. The condition of 0.2 M NaCl with pH 5.0 was observed to provide optimum LOX stability. The enzyme activity was reduced by addition of cations, $Mn^{2+},\;Cu^{2+}\;or\; Al^{3+}$, except $Ca^{2+}$ which stimulated activity of LOX. Butylated hydroxy anisole (BHA) and propyl gallate decreased LOX activity with increasing concentration. Cucumber peel had higher activity than other tissues, locule or mesocarp, of cucumber.

• Journal of the Korean Chemical Society
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• v.24 no.1
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• pp.34-43
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• 1980

The reaction of thianthrene cation radical perchlorate with thioxanthene in acetonitrile gave thianthrene and dark reddish thioxanthylium ion instead of thioxanthene cation radical. Addition of aromatic nucleophiles such as anisole, aniline, N,N-diethylaniline, catechol, ethylbenzene, to the above mixture yielded the corresponding thioxanthenes with substituent at 9 position. Reactions with dibenzo-18-crown-6-ether, diphenylmercury, and triphenylphosphine gave similar products. However, reactions with aromatics with electron-withdrawing group were either too slow or inert to such a reaction.

• Textile Coloration and Finishing
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• v.13 no.6
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• pp.381-390
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• 2001

The optimum carrier concentrations were obtained by the maxmium exhaustion ratios of polyester fabrics at 8$0^{\circ}C$ . The optimum concentrations of methylsalicylate, acetophenone, anisole, propiophenone, 2-ethyl hexyl alcohol, ethylene glycol and propylene glycol were $3g/\ell,\;12g/\ell,\;7g/\ell,\;5g/\ell,\;3g/\ell,\;35g/\ell,\;and\;40g/\ell$, respectively Azo, anthraquinone, and quinoline disperse dyes were quite stable up to PH 10.3, but nitro disperse dye were severely hydrolyzed in alkaline dyeing. The tensile strength decreased with increasing dyebath pH because the polyester fabrics were easily decomposed by alkali. The reduction cleaning could be canceled in alkaline dyeing because the carriers were solved by alkali during dyeing.

• Textile Coloration and Finishing
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• v.13 no.6
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• pp.23-23
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• 2001

The optimum carrier concentrations were obtained by the maxmium exhaustion ratios of polyester fabrics at 80℃. The optimum concentrations of methylsalicylate, acetophenone, anisole, propiophenone, 2-ethyl hexyl alcohol, ethylene glycol and propylene glycol were 3g/ℓ, 12g/ℓ, 7g/ℓ, 5g/ℓ, 3g/ℓ, 35g/ℓ, and 40g/ℓ, respectively. Azo, anthraquinone, and quinoline disperse dyes were quite stable up to pH 10.3, but nitro disperse dye were severely hydrolyzed in alkaline dyeing. The tensile strength decreased with increasing dyebath pH because the polyester fabrics were easily decomposed by alkali. The reduction cleaning could be canceled in alkaline dyeing because the carriers were solved by alkali during dyeing.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1994.04a
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• pp.328-328
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• 1994

광독성 및 광알러지를 일으키는 제반 약물이나 화학물질의 안정성과생체 이용율을 높이고 현재까지 확실하게 규명되어있지 않은 약물 및 화학물질에의한 광독성 광알러지성의 기전을 이해하고 설명할수있는 학문적 기초를 확립 하고저 phenothiazines 중 몇가지 약물를 택하여 적혈구를 이용한 광용혈 여부와 이에 미치는 ascorbic acid, butyl hydroxy anisole, dibutyl hydroxy toluene의 영향을 조사하였다. 각 약물 농도를 50$\mu\textrm{g}$/m1로 하고 UVA(350nm.2.5 ㎽/cm)조사시간은 30분으로 하여 적혈구의 광용혈현상을 Kahn등의 방법에의해 spectrophotometer로 측정한결과 chlorpromazine, perphenazine, thioridazine매 의한 광용혈정도는 ascorbic acid에의해 유의성 있게 감소되었다. 또한 적혈구를 가하기 전 각 약물을 미리조사시켜 생성된 물질에의한 광용혈현상의 광독성생성물질은 chlor- promazine과 thioridazine에서 보여졌으며, chlorpromazine의 광독성생성물질에 의한 적혈구 용혈현상만 ascorbic acid에의해 감소되었다.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.316-316
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• 2006

The preparation of an organic/inorganic polymer hybrid from a novolac derivatives is described. The hybrid was prepared by the acid-catalyzed solgel reaction of phenyl-trimethoxysilane (PhTMOS) in the presence of anisole novolac. The resulting film was transparent and showed a high heat stability. The dispersion of two components might be due to the utilization of the p-p interaction between the phenyl ring of the silica matrix and that of novolac. This makes it possible to prepare a hybrid glass having a highly content of novolac derivatives.

• Natural Product Sciences
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• v.8 no.1
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• pp.26-29
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• 2002

The MeOH extract of Sorbus commixta (Rosaceae) exhibited strong DPPH radical scavenging activity, and through activity-guided fractionation two antioxidant compounds were isolated and identified as $catechin-7-O-{\beta}-D-xylopyranoside$ (1) and $catechin-7-O-\;{\beta}-D-apiofuranoside$ (2) by physicochemical and spectrometric methods. To evaluate the antioxidant effect of these compounds, some in vitro tests, such as the DPPH radical scavenging activity test, the superoxide radical scavenging activity test and the lipid peroxidation inhibitory activity test, were performed. Compounds 1 and 2 showed stronger activities than both a-tocopherol and butylated hydroxy anisole (BHA) in each assay.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1993.04a
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• pp.122-122
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• 1993

살균, 정균, 살진균, 정진균등의 효능이 있는 나프토퀴논꼴 화합물인 6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2,2-dimethylnaphtho [1,2] pyran(1)과 그의 유도체인 9-methoxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaphtho [1,2] pyran(2), 8,9-dimethoxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaph-the [1,2] pyran(3), 9-bromomethyl-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethyl-naphtho [1,2] pyran(4)와 8, 9-methylenedioxy-6-oxo-3, 4, 4a, 5-tetrahydro-3-hydroxy-2, 2-dimethylnaphtho [1,2] pyran(5)을 손쉽게 구할 수 있는 benzene, anisole, 1, 2-di-methoxybenzene, bromomethylbenzene, 1, 3-benzodioxole등을 원료로 하여 합성하는 것이 본 연구의 목적이다.

• YAKHAK HOEJI
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• v.50 no.6
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• pp.393-397
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• 2006

The synthesis of new 3-substituted 7-halocephalosporanates was described. 7-ACA was reacted with thiols at pH 6.5${\sim}$6.8 to afford the 3-substituted 7-ACA (1), which was treated with diphenyldiazomethane to give diphenylmethyl 7-aminocephalosporanate (2). The Halogenation of 7-aminocephalosporanate (2) with NaNO$_2$, KBr and H$_2$SO$_4$ gave 7-bro-mocephalosporanate (3) and with NaNO$_2$, HCI gave 7-chlorocephalosporanate (4). Diphenylmethyl cephalosporanate (2${\sim}$4) were deprotected by AIC1$_3$ in anisole and neutralized to give the sodium cephalosporanate (5${\sim}$7).