• 한국식품과학회지
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• 제21권4호
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• pp.562-568
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• 1989

9월 중에 채취한 성숙한 초피 (Zanthoxylum piperitum DC)의 과피와 잎성분의 변성을 고려한 방법인 gas co-distillation으로 추출하고, GC/MS와 함께 workstation BASIC program들을 사용하여 극성이 다른 두 column(FFAP, HP-1)에 대한 authentic standard들의 retention index(RI) 값들을 구하여 HP-1 및 FFAP, RI reference library를 만든 후 초피의 정유성분들의 두 column library 탐색을 병행하여 분석함으로써, 과피에서 myrcene외 14 hydrocarbon들, linalool외 8 alcohol들, citronellal외 3 aldethyde들, carvone외 2 ketone들, methyl salicylate외 7 ester들 그리고 1,8-cineol 외 3 oxide를 확인하였고, 잎에서 limonene외 7 hydrocarbon들, citronellol외 7 alcohol들, cumin aldehyde외 1 aldehyde, carvone, 그리고 estragole외 1 oxide를 확인하였다. 과피에서는 1,8-cineol(25.47%), limonene(11.9%), geranylacetate(9.01%), myrcene(6.15%), geraniol(2.88%), citronellal(2.25%)등이 주성분이었고, 잎에서는 citronellal(23.11%), 1,8-cineol(18.38%), citronellol(6.04%), methyl cinnamate(4.08%)등이 주성분이었다.

• 대한화학회지
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• 제30권6호
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• pp.548-552
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• 1986

(${\pm}$)시스- 및 트란스-3-(2,2-디클로로비닐)-2,2-디메틸-1-시클로프로판 카르복시산 3-페녹시벤질을 2-메틸-3-부텐-2올($\underline{2}$)을 출발물질로하여 입체선택적으로 합성하였다. 아세트산과 무수아세트산의 존재하에서 2-메틸-3-부텐-2-올을 알릴자리옮김 반응에 의해 아세트산3-메틸-2-부텐-일($\underline{3}$)을 얻은 다음 이 아세트산 알릴($\underline{3}$)의 [3,3] 시그마 자리옮김 반응에 의해 ${\gamma},\;{\delta}$-불포화산($\underline{4}$)을 얻었다. 3,3-디메틸-4-펜텐산($\underline{4}$)을 SOCl$_2$로 처리하고 3-페녹시벤질알코올로 에스테르화 시켜 알코올 부분이 구축된 3,3-디메틸-4-펜텐산 3-페녹시벤질($\underline{6}$)을 얻어서 사염화탄소의 첨가 후 그리화에 의해 (+)시스-및 트란스-3-(2,2-디클로로비닐)-2,2-디메틸-1-시클로프로 판카르복시산 3-페녹시벤질을 합성하였다

• Bulletin of the Korean Chemical Society
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• 제12권5호
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• pp.569-574
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• 1991

Methyl red diffusion in polymer solutions was studied by a transient holographic method, forced Rayleigh scattering. In semi-dilute solutions of a polystyrene, where no specific interaction with the probe exists, we found within experimental uncertainty that the retardation of diffusion rate of methyl red is independent of the solvents used. This indicates that the hydrodynamic interaction in polymer coils is not affected by the nature of solvents enough to exhibit a detectable change in the diffusion rate of the probe. On the other hand, a substantial reduction of diffusion rate was observed in poly(methyl methacrylate) solutions in toluene. Together with the similar observation reported with poly(vinyl acetate), it is confirmed that hydrogen bond between the probe and the polymer is responsible for the retarded diffusion. The decay-growth-decay profile found in this system reveals a finite difference in diffusion coefficients of cis and trans isomer of methyl red. We estimate the difference and suggest that the cis isomer interacts with the polymer more strongly than the trans isomer.

• 환경위생공학
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• 제16권1호
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• pp.72-90
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• 2001

This study was conducted to evaluate desorption efficiencies accuracy and precision by $CS_2$ and thermal desorption method for polar and non-polar organic solvents collected on activated carbon(AC), activated carbon fiber(ACF), carbosieve SIII, materials tested were Methyl alcohol, n-Hexane, Benzene, Trichloroethylene, Methyl isobutyl ketone and methyl cellosolve acetate and six different concentration levels of samples were made. The results were as follows ; 1. Accuracy on kind adsorbent and desorption method was low. In case of $CS_2$ desorption solvent, Overall B and Overall CV on AC and ACF were 43% and 6.63%, respectively. In case of thermal desorption method, accuracy of thermal desorption method appeared higher than solvent desorption method by AC 18.0%, 3.54%, ACF 2.6%, 2.57%, Carbosieve SIII 13.7% and 1.97%, respectively. 2. In the concentration level III, accuracy of thermal desorption method on adsorbent was in order as follow ; ACF > Carbosieve SIII > AC in the methyl alcohol and Carbosieve SIII > ACF > AC in the rest of them all subject material and Concentration levels showed good precision at EPA recommend standard (${\leq}{\;}30%$) 3. DEs by type of organic solvent adsorbent and desorption method are as follows ; In the case that desorption solvent is $CS_2$, DE of Methyl alcohol is AC 47.5%, DE of all materials is ACF about 50%. In the case of thermal desorption method, DE of Methyl alcohol is AC 82.0%, ACF 97.4%, Carbosieve SIII 86.3%. DE of the later case is prominently improved more than one of former. In particular, Except that DE of EGMEA is ACF 88.5%, DE of the rest of it is more than 95% which is recommend standard MDHS 72. With the result of this study, in order to measure various organic solvent occurring from the working environment, in the case of thermal desorption method, we can get the accurate exposure assessment, reduce the cost, and use ACF as thermal desorption sorbent which available with easy.

• 분석과학
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• 제31권6호
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• pp.225-231
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• 2018

안식향산, 메틸파라벤, 부틸파라벤은 식품, 의약품뿐 만 아니라 화장품 분야에서도 사용되는 보존료이다. 그러나 이들 보존료들의 여러 가지 독성이 보고되면서, 한국을 비롯하여 여러 나라들에서 식품 중의 이들 보존료의 사용을 규제하고 있다. 본 연구에서는 간장 중의 안식향산, 메틸파라벤, 부틸파라벤의 정확하고 정밀한 분석을 위하여 세가지 분석물질의 동위원소를 내부표준물질로 이용하는 동위원소 희석 액체크로마토그래피 질량분석법 (Isotope Dilution Liquid Chromatography Mass Spectrometry, ID-LC/MS)을 개발하였다. 메틸, 부틸 파라벤보다 pKa가 낮은 안식향산을 고려하여 acetic acid로 pH 4.0으로 조정한 5 mM ammonium acetate를 이동상 용매로 사용하여 C18 컬럼으로 분리하였다. 질량분석 조건으로는 전기분무이온화법으로 음이온을 생성하여 음이온 모드에서 분석하였으며, 방해물질로부터 선택성을 향상하기 위해 선택반응분석법 (Selected Reaction Monitoring)을 이용하여 분석하였다. 간장의 색깔과 간장 중의 여러 가지 방해물질들을 제거하기 위하여 C18 카트리지를 이용하여 정제하였다. 최적화된 조건과 방법을 이용하여 싱가포르 Health Science Authority(HSA)가 제공하는 간장 기준시료를 분석하였다. 본 연구원에서 측정한 결과값은 HSA가 제공하는 기준값과 불확도 내에서 일치하였다.

• 한국재료학회지
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• 제15권10호
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• pp.678-682
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• 2005

We studied the possibility of $Zn_4O(Ac)_2(OH)$ formation as a precursor for ZnO nano particles in sol-gel method. Four different additives such as tetra methyl ammonium hydroxide, mono ethanol amine (MEA), LiOH, and $H_2O$ were used for zinc acetate dissolved in 2-methoxy ethanol. ZnO particles of 5-6 nm in size were observed. Existence of $Zn_4O(Ac)_6$ was not verified. $Zn_4O(Ac)_2(OH)$ molecules were observed and they were believed to be the precursors of ZnO. A peak at 275nm in UV-Vis analysis was observed In the case of MEA and $H_2O$ but no ZnO particles were detected in transmission electron microscopy.

• 한국환경독성학회:학술대회논문집
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• 한국환경독성학회 2002년도 추계국제학술대회
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• pp.153-153
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• 2002

수돗물의 염소소독 과정에서 부식질의 초기 분해생성물인 MX(Mutagen X)는 수돗물의 전체 돌연변이유발성의 최고 60%까지 차지하는 것으로 알려져 있다. 그러나 존재하는 농도는 수 ng/L로 정량분석을 위해서는 resin을 사용하여 10 ~ 20L의 물을 농축하여야 한다. 이 연구에서 MX의 농축에 사용된 resin은 XAD-4와 XAD-7HP의 1:1 mixture이었으며, 사용 전에 Soxhlet extractor를 사용하여 ethyl acetate와 methanol로 각각 12시간씩 세척하였다. 15L의 물 시료는 37%의 염산으로 pH 2에 맞춘 후 직경 2cm의 유리관에 15cm의 높이로 채워진 resin을 40mL/min의 유속으로 통과시켰다. 유리관에 잔류하는 물은 질소가스로 대부분 불어 제거한 후 ethyl acetate 200mL를 가해 1mL/min의 유속으로 흘려주어 MX를 용출시킨 후 회전증발기로 5mL의 부피까지 농축시키고 10% H$_2$SO$_4$ in MeOH 0.1mL를 가하여 6$0^{\circ}C$에서 methyl ester화하였다. 과포화된 $Na_2$SO$_4$ 수용액 0.3ml를 가한 후 MTBE 0.3mL로 추출하고 GC/ECD로 분석하였다. MX의 회수율은 60% 이상이었으며 일부수돗물 시료에 대해 분석하였다.

• 대한화학회지
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• 제14권3호
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• pp.221-228
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• 1970

The tendency of forming a charge transfer complex between furfuryl derivatives (2-methyl furan, furfuryl acetate, and Ethyl 2-furoate) and halides(Iodine, Iodine monochloride, and Trichloro bromo methane) was studied by means of ultra violet spectrophotometry. In case of furfuryl acetate the formation of the complex could not be distinctly detected by this method. Iodine and trichloro bromo methane could show a distinct formation of charge transfer complex in the U.V. region, whereas iodine monochloride shows a possibility of forming an addition compound rather than the charge transfer complex itself. The results were discussed in conjunction with the stability of the furfuryl ring.

• 한국식품영양과학회지
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• 제29권2호
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• pp.316-321
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• 2000

This study carried out to eluciate the cancer chemoprevention of Korean native fermented food, baechu kimchi using Comet assay (in other words, single cell microgel electrophoresis). For this purpose, baechu kimchi was fractionated by water, n-hexane, chloroform and ethyl acetate. 5 strains of dominant fermented bacteria were isolated from baechu kimchi. The water fraction, n-hexane fraction, chloroform fraction, ethyl acetate fraction and water insoluble fractions showed no antigenotoxicitie in non-tumoral normal 3T3 cells. Among 5 bacteria isolates from baechu kimchi, two isolates bacteria 1 and 2 strongly inhibited genotoxicity of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) in non-tumoral normal 3T3 cells (p<0.05). Bacteria 3, 4 and 5 were also not antigenotoxic.

• Archives of Pharmacal Research
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• 제26권9호
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• pp.686-696
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• 2003

Ethyl (coumarin-4-oxy)acetate 1 was prepared through the reaction of 4-hydroxycoumarin with ethyl bromoacetate. Compound 1 was allowed to react with hydrazine hydrate to produce coumarin-4-oxyacetic hydrazide 2. The synthesis of N-(arylidene and alkylidene)-coumarin-4-oxyacetic hydrazones 3-20 was performed. The preparation of 2-substituted-3-[(coumarin-4-oxy) acetamido]thiazolidinones 21-26 and 2-[(coumarin-4-oxy )methyl]-4-acetyl-5-substituted-$\Delta^2$-1,3,4-oxadiazolines 27-33 was performed by the reaction of the hydrazones 3, 4, 7, 9, 12, 14 with mercaptoacetic acid and the hydrazones 3, 4, 5, 7, 12, 15, 16 with acetic anhydride, respectively. The antiviral activities, cytotoxicities and structure-activity relationship (SAR) towards different microorganisms of the prepared compounds were studied.