• Bulletin of the Korean Chemical Society
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• 제17권7호
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• pp.625-630
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• 1996

The cobalt-substituted polyoxotungstate [(CoPW11O39)5-] has been used as a catalyst in olefin epoxidation and alkane hydroxylation reactions. The epoxidation of olefins by iodosylbenzene in CH3CN yielded epoxides predominantly with trace amounts of allylic oxidation products. cis-Stilbene was streoselectively oxidized to cis-stilbene oxide with small amounts of trans-stilbene oxide and benzaldehyde formation. The epoxidation of carbamazepine (CBZ) by potassium monopersulfate in aqueous solution gave the corresponding CBZ 10,11-oxide product. Other transition metal-substituted polyoxotungstates (M=Mn2+, Fe2+, Ni2+, and Cu2+) were inactive in the CBZ epoxidation reaction. The cobalt-substituted polyoxotungstate also catalyzed the oxidation of alkanes with m-chloroperbenzoic acid to give the corresponding alcohols and ketones. The presence of CH2Br2 in the hydroxylation of cyclohexane afforded the formation of bromocyclohexane, suggesting the participation of cyclohexyl radical. In the 18O-labeled water experiment, there was no incorporation of 18O into the cyclohexanol product when the hydroxylation of cyclohexane by MCPBA was carried out in the presence of H218O. Some mechanistic aspects are discussed as well.

• 한국환경보건학회:학술대회논문집
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• 한국환경보건학회 2003년도 Challenges and Achievements in Environmental Health
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• pp.157-157
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• 2003

To evaluate an effect of pathological liver damage on the cyclohexane metabolism, rats were pretreated with 50% $CCl_4$ dissolved in olive oil (0.1$\mell$/100g body weight) 10 or 17 times intraperitoneally at intervals of every other day. On the basis of liver function and histological findings, the animals pretreated with $CCl_4$ 10 times were identified as acutely liver damaged ones and the animals pretreated with $CCl_4$ 17 times were identified as severly liver damaged ones, with fibrosis, biliary abnormality and mild injury both in the kidneys and the lungs. To these liver damaged animals, cyclohexane (a single dose of 1.56g/kg body weight, i.p.) was administrated at 48 hours after the last injection of $CCl_4$. The rats were sacrificed at 4 or 8 hours after injection of cyclohexane. The cyclohexane metabolites; cyclohexanol (CH-ol), cyclohexane-1, 2-diol (CH-1, 2-diol), cyclohexane-l, 4-diol (CH-1, 4-diol), and their glucuronyl conjugates and cyclohexanone (CH-one) were detected in the urine of cyclohexane treated rats. After cyclohexane treatment, the serum levels of CH-ol and CH-one were remarkably increased at 4 hours and then decreased at 8 hours in normal group. Whereas in liver damaged rats, these cyclohexane metabolites were higher at 8 hours than at 4 hours. The excretion rate of cyclohexane metabolites from serum into urine was more decreased in liver damaged animals than normal group, with the levels of excretion rate being lower in $CCl_4$ 17 times injected animals than 10 times injected ones. However, it was interesting that the urinary concentration of cyclohexane metabolites was generally more increased in liver damaged animals than normal ones, and the increasing rate was higher in $CCl_4$ 17 times injected rats than 10 times injected ones. And liver damaged rats, especially $CCl_4$ 17 times treated ones, had an enhanced ability of glucuronyl conjugation to cyclohexanol analogues compared with normal group. Futhermore, CH-1, 2 and 1, 4-diol were all conjugated with glucuronic acid in $CCl_4$ 17 times injected animals. In conclusion, the metabolic rate of cyclohexane was unexpectably accelerated and it may be caused by physiological adaptation of adjacent intact hepatocyte in damaged liver.

• 한국식품영양학회지
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• 제10권1호
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• pp.25-30
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• 1997

Purge와 trap headspace sampler를 사용하여 녹차의 휘발성 성분을 추출, 확인한 후 성분조성을 동시증류추출장치로 추출된 성분가 비교하였다. Headspace법으로는 88개 성분을 확인하였으며 methyl butanal(3.1%), 1-penten-3-ol(5.48%), 2-penten-1-ol(2.89%), hexanal(5.77%), heptanal(2.24%) 등의 비교적 비점이 낮은 성분들과 2,4-heptadienal(4.28%), linalool(2.27%), nonanal(2.06%), 2,6-dimethyl cyclohexanol(2.57%) 및 $\alpha$-pinene(1.52%), caryophyllene(1.70%) 등의 hydrocarbon 화합물, $\beta$-cyclocitral(2.0%), $\alpha$-ionone(2.62%), $\beta$-ionone(2.98%) 같은 carbonyl 화합물이 주요 휘발성 성분으로 확인되었다. SDE법으로는 64개의 성분을 확인하였으며 저비점 성분들보다는 benzyl alcohol(3.79%), linalool(9.52%), terpineol(2.16%), geraniol(2.75%), nerolidol(6.50%) 등의 alcohol 성분들과 $\alpha$-ionone(1.77%), $\beta$-ionone(4.80%), geranyl acetone(1.82%) 등의 ketone 화합물, hexanoic acid(1.45%), nonanoic acid(1.11%) 등의 acid 화합물이 주요 성분으로 확인되었다.

• 농업생명과학연구
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• 제45권6호
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• pp.141-150
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• 2011

저염 우렁쉥이 젓갈의 풍미발현물질을 구명하기 위해 SDE apparatus, GC 및 GC/MS를 이용하여 저염 우렁쉥이 젓갈 특유의 향기성분을 추출, 분리 및 동정하였다. $5^{\circ}C$에서 15일간 숙성시킨 저염 우렁쉥이 젓갈의 pH는 5.17, 염도는 8.0%, 휘발성염기질소의 함량은 23.0 mg/100 g이었다. 저염 우렁쉥이 젓갈의 향기성분으로 총 96 성분이 동정되었고, 총함량은 $1,221.42{\mu}g/100g$-cyclohexanol이었다. 이들 화합물의 종류와 함량을 group별로 분류하면 alcohol류 23종, acid류 16종, aldehyde류 15종, hydrocarbon류 29종, 방향족 화합물 6종, ester류 2종, 함질소 화합물 2종 및 기타 3종으로 구성되어 있었는데, 계수적인 측면에서 가장 많은 화합물은 hydrocarbon류였고, 양적인 측면에서 가장 많은 화합물은 1-octanol을 위주로 한 alcohol류였다. 저염 우렁쉥이 젓갈의 향기발현에는 alcohol류를 위주로 여기에 aldehyde류, acid류, 방향족 화합물, ester류 및 함질소 화합물 등이 관여하며, 이들 성분이 서로 조화를 이루어 저염 우렁쉥이 젓갈의 독특한 향기를 발현한다고 생각되었다.

• 공업화학
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• 제34권3호
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• pp.252-257
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• 2023

본 연구에서는 내분비계 교란 물질로 알려진 프탈레이트계 가소제를 대체하기 위하여 동·식물성 오일로부터 추출되는 지방산과 고리를 포함하는 알코올을 이용하여 가소제 후보물질을 합성하고, 가소화 효율을 포함한 가소제로서의 특성을 평가하였다. 지방산 3종(caprylic acid, capric acid, lauric acid)과 알코올 3종(solketal, benzyl alcohol, cyclohexanol)의 에스터화 반응으로 합성한 9종의 화합물의 구조는 ¹H-NMR을 이용하여 확인하였다. 합성한 9종의 가소제 후보물질은 PVC 수지에 첨가하여 가소 특성을 평가하였고, 상용 가소제인 di-2-ethylhexyl phthalate (DEHP), di(isononyl)cyclohexane-1,2-dicarboxylates (DINCH), epoxidized soybean oil (ESO)과 비교·분석하여 대체 가소제로서의 가능성을 평가하였다. 결과에 따르면 가소화 효율은 DEHP 대비 0.96~1.02 배, ESO 대비 0.94~0.98 배로 비슷한 결과를 얻었으며, DINCH의 경우보다는 1.05~1.10 배 우수한 결과를 보였다. 열적 안정성은 DEHP, DINCH보다 다소 떨어지나 ESO의 경우보다는 우수한 결과를 나타내었다. 용출성 시험 결과, 수성용매인 물과 유성용매인 노말 헥세인에서 DEHP, DINCH보다 다소 높은 결과를 보였으나 ESO 대비 유사하거나 우수한 특성을 나타내는 것을 확인하였다.

• Journal of Pharmaceutical Investigation
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• 제37권2호
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• pp.101-106
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• 2007

Venlafaxine, 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl] cyclohexanol hydrochloride is a novel, nontricyclic antidepressant. venlafaxine is a unique antidepressant that differs structurally from other currently available. The aim ot the study was to formulate sustained-release venlafaxine granules and assess their formulation variables. It consists of two layers, venlafaxine drug layer and sustained release coating layer and manufactured by fluidized bed process. The sustained release of drug could be increased by double-control rising various components in venlafaxine drug layer and sustained-release layer. The drug-containing granules were coated with cellulose acetate, cetyl alcohol and Eudragit RS along with plastisizer such as dibuthyl sebacate as an nano-pore former The release oi venlafaxine depended on the type of Eudragit such as RS, and RL used in the formulation of controlled release layer. These results obtained clearly suggest that the sustained release oral delivery system for venlafaxine could be designed with satisfying drug release profile approved.

• 대한의생명과학회지
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• 제12권4호
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• pp.361-370
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• 2006

To evaluate an effect of pathological liver damage on the conjugation of cyclohexane metabolites, rats were pretreated with 50% $CCl_4$ dissolved in olive oil (0.1 ml/100 g body weight) 10 or 17 times intraperitoneally at intervals of every other day. On the basis of liver function, the animals pretreated with $CCl_4$ 10 times were identified as acutely liver damaged ones and the animals pretreated with $CCl_4$ 17 times were identified as severly liver damaged ones. To these liver damaged animals, cyclohexane (a single dose of 1.56 g/kg body weight, i.p.) was administered at 48 hr after the last injection of $CCl_4$. The rats were sacrificed at 4 or 8 hr after injection of cyclohexane. The cyclohexane metabolites, cyclohexanol (CH-ol), cyclohexane-1,2-diol (CH-1,2-diol), cyclohexane-1,4-diol (CH-1,4-diol), and their glucuronyl conjugates and cyclohexanone were detected in the urine of cyclohexane treated rats. The urinary concentration of cyclohexane metabolites was generally more increased in liver damaged animals than normal ones, and the increasing rate was higher in $CCl_4$ 17 times injected rats than 10 times injected ones. And liver damaged.ats, especially $CCl_4$ 17 times treated ones, had an enhanced ability of glucuronyl conjugation to CH-ol analogues compared with normal group. Futhermore, CH-1,2 and 1,4-diol were all conjugated with glucuronic acid in $CCl_4$ 17 times injected animals. On the other hand, the increasing rate of activities of hepatic cytochrome P450 dependent aniline hydroxylase, alcohol dehydrogenase and urine diphosphate glucuronyl transferase was higher in 17 times $CCl_4$-treated rats compared with normal and $CCl_4$ 10 times injected animals. Taken all together, it is assumed that an increased urinary excretion amount of cyclohexane metabolites in liver damaged rats might be caused by an increase in the activities of cyclohexane metabolizing enzymes. And enhanced conjugating ability of CH-ol in liver damaged animals and novel finding of conjugating form of CH-1,2 and 1,4-diol might be caused by increase in the activity of hepatic diphosphouridine glucuronyltransferase.

• 약학회지
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• 제11권1_2호
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• pp.7-16
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• 1967

A yellowish microneedles, $C_{28}$ H$_{32}$ $O_{14}$ ${\cdot}$ I$_{1}$/$_2$, H$_{2}$O, m.p.262-$4^{\circ}$ , [${\alpha}$$_{D}^{20}$= -71,$43^{\circ}$(C = 0.42, pyridine), its acetate m.p.123-5.deg., were obtained in 0.3% yield from the leaves of Chrysanthemum sibiricum F$_{ISCHER}$. This substance is insoluble in water and the usual organic solvents except pyridine and ethylene glycol and, is not decomposed by dilute mineral acids but undergoes decomposition on being boiled in 60% H$_{2}$SO$_{4}$ or 35% HCl, giving one moel each of acacetin, glucose and rhamnose. It was not hydrolysed with a rhamnodiastase preparation obtained from the seeds of Rhamnus koraiensis. After permethylation of it, the uncrystallized product was hydrolysed and apigenin-5,4'-dimethyl ehter, m.p.$262^{\circ}$ was obtained, indicating that the disaccharide residue is at the 7 position of acacetin. Partial hydrolysis of this acacetin-7-rhamnoglucoside in cyclohexanol with formic acid gave acacetin-7-glucoside, m.p.246.deg. and rutinose, identifying them with authentic specimen on a paper chromatography. It was thus identified as linarin(acacetin-7-rutinoside) by means of mixed fusion, of paper partition chromatography and of its derivatives. Zemplen and Bognar suggested that the glucosidic linkage of linarin is .betha. by means of synthesis of this substance. But there is no evidence whether it is hydrolysed by emulsin or maltase or not. Linarin itself was not hydrolysed by an emulsin existing in the seed of Apricot or a maltase, but acacetin-7-glucoside(tilianin) which obtained from linarin gave acacetin and glucose on hydrolysis with the same emulsin and accordingly the glucosidic linkages of linarin and tilianin are thus regarded as ${\beta}$.

• Nuclear Engineering and Technology
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• 제47권6호
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• pp.738-745
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• 2015

The catalytic exchange of hydrogen isotopes between hydrogen and water has been known to be a very useful process for the separation of tritium from tritiated water. For the process, a highly active hydrophobic catalyst is needed. This study provides an effective fabrication method of size-controlled platinum/poly[styrene-divinylbenzene-tri(propylene glycol) diacrylate] [Pt/poly(SDB-TPGDA)] hydrophobic catalyst beads with a narrow size distribution. Platinum nanoparticles were prepared by ${\gamma}$-ray-induced reduction in the aqueous phase first, and then uniformly dispersed in SDB-TPGDA comonomer after the hydrophobization of platinum nanoparticles with alkylamine stabilizers. The porous Pt/poly(SDB-TPGDA) hydrophobic catalyst beads were synthesized by the UV-initiated polymerization of the mixture droplets prepared in a capillary-based microfluidic system. The size of as-prepared catalyst beads can be controlled in the range of $200-1,000{\mu}m$ by adjusting the flow rate of dispersed and continuous phases, as well as the viscosity of the continuous phase. Sorbitan monooleate and cyclohexanol were used as coporogens to control the porosities of the catalyst beads.

• 공업화학
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• 제10권1호
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• pp.124-128
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• 1999

개별적인 반응성이 알려진 니트로기와 벤질술포닐기가 벤젠 고리 위에서 서로 인접하여 위치할 때 광반응성에 미치는 상호 작용에 대해서 연구하고자 하였다. 니트로기를 포함하는 술포닐 에스테르(cyclohexyl 및 phenyl 2-nitro-${\alpha}$-toluenesulfonate)와 슬포닐아미드(시클로헥실, 페닐, 벤질, 및 피페리딜 2-nitro-${\alpha}$-toluenesulfonamide)의 용액 중 광반응 생성물로부터 벤질술포닐기와 그 ortho 위치에 존재하는 니트로기가 광반응시 서로 상승작용을 하지 않는다는 것을 알 수 있었다. 용액상의 광반응은 이어 필름 상에서의 광반응으로 확인 및 응용되었다. 즉, 두 가지의 2-nitro-${\alpha}$-toluensulfonamide를 포함한 poly(methacrylonitrile)(PMAN) 박막을 NaCl 판 위에 입히고 여기에 254 nm 자외선을 쪼이면서 관찰된 필름의 IR 스펙트럼의 변화로부터도 용액상의 광반응을 일부 확인하였으며 정량실험도 실시하였다. 또한, 본 용액실험의 결과인 광화학적 아민 발생은 poly(glycidyl methacrylate)를 이용한 상 발생 실험에 응용되어 성공적으로 광화학적 에폭시 가교를 수행할 수 있었다.