• 한국응용과학기술학회지
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• 제30권1호
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• pp.152-159
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• 2013

폴리글리세롤에스터 유화제를 이용한 에멀젼의 입자상태 및 시간의 변화에 따른 안정성을 여러 가지 오일을 이용하여 실험을 실시하였다. 실험결과 오일의 종류에 따라 입자크기 및 안정성에 있어서 다소의 차이가 있는 것을 확인하였다. 폴리글리세롤 에스터로 유화된 가장 안정한 오일은 polar 오일인 실리콘계열과 지방산에스터 오일이고, 탄화수소계열의 nonpolar오일(Mineral oil, squalane, polydecene) 등이 유화에 있어서 가장 불안한 상태를 보였다. 식물성오일도 폴리글리세릴 에스터 유화제와는 안정한 형태의 입자형성을 보였다.

• Tribology and Lubricants
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• 제17권2호
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• pp.109-115
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• 2001

The lubricating performance of 23 kinds of polyol ester base oils 〔POEs〕 having different branch shapes was investigated by using a four ball tribometer under boundary lubrication condition. All the polyol ester base oils used in this study were made up of polyhydric alcohols of two-four valence and normal or branched fatty acids of different carbon number. The wear characteristics of polyol ester base oils are different from those of mineral oil, strongly affected by the branch shapes of fatty acids in their molecles. In particular, the polyol ester base oils having normal fatty acids such as n-octanoic acid, n-nonanoic acid etc. show much better wear performance than POEs having branched fatty acids such as 2-ethylhexanoic acid, 3,5,5-trimethyl hexanoic acid, etc. As the carbon chain length of normal fatty acids, in case of POEs of normal fatty acids, is increased, their wear rate is decreased and, in case of POEs of branched fatty acids, as the degree of branch of branched fatty acids is decreased, their wear rate is decreased. All the wear results of polyol ester base oils could be reasonably explained by comparing cohesive ability among fatty acid molecules in adsorption film by fatty acids obtained as POEs were decomposed.

• 약학회지
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• 제33권5호
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• pp.290-295
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• 1989

2,6-Dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid methyl ester (1) was formylated to 2,6-dimethy-4-(3'-nitrophenyl)-5-formyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (2) in 76% yield. At the elevated temperature, 2,6-dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-monomethyl ester (3) was also converted into compound 2 in 46% yield. The compound 2 was reduced to 2,6-dimethyl-4-(3'-nitrophenyl)-5-hydroxymethyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (4) in 91% yield. Compound 2 was reacted with triethyl phosphonoacetate to give 2,6-dimethyl-4-(3'-nitrophenyl)-5-(2-ethoxycarbonyl ethenyl)-1,4-dihydropyridine-3-carboxylic acid methyl ester (5) in 50% yield. Reaction between compound 2 and amines (methyl amine, ethylamine, methoxylamine, hydroxyl amine, phenyl hydrazine and 1-amino-4-methyl piperazine) gave six schiff bases 7a, 7b, 7c, 7e, 7f in 81%, 91%, 82%, 81%, 50% and 84% yield, respectively.

• 약학회지
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• 제33권5호
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• pp.280-284
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• 1989

When 2,6-Dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-mono methyl ester(3) was reacted with dimethyl methylene ammonium chloride (5a) and $K_2CO_3$ in DMF, 2,6-dimethyl-4-(3'-nitrophenyl)-5-(N,N-dimethylamino)methyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (6a) was obtained in 41% yield. As the same procedure with compound (3) and the other dialkylaminomethylating reagents (5b, c, d, e), 2,6-dimethyl-4-(3'-nitrophenyl)-5-(N,N-diethylamino)methyl-1,4-dihydropyridine-3-carboxylic acid methylester(6b), 2,6-dimethyl-4-(3'-nitrophenyl)-5-(1'-pyrrolidinyl)methyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (6c), 2,6-dimethyl-4-(3'-nitrophenyl)-5-(1'-piperidinyl)methyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (6d) and 2,6-dimethyl-4-(3'-nitrophenyl)-5-(1'-morpholinyl)methyl-1,4-dihydropyridine-3-carboxylic acid methyl ester (6e) were obtained in 28%, 49%, 48% and 18% yield respectively.

• Archives of Pharmacal Research
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• 제12권1호
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• pp.17-21
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• 1989

We have reported earlier on the reactivity of 7-dithiocarboxy-3-phenyl-5,6-dihydro imidazo[2,1-b]thiazolium-betaine with several para-substituted phenacyl bromides. In this work reactions of 7-dithiocarboxy-3-phenyl(or methyl)-5,6-dihydro imidazo[2,1-b]thiazolium-betaine with a series of aliphatic alkylating agents of ${\alpha}$ -halo ketone,${\gamma}$-halo koto ester and ${\alpha}$ -halo ester were examined for the similar purpose. In case of ${\alpha}$-halo ketone or ${\gamma}$-halo koto ester such as ${\alpha}$ -chloro acetone or ethyl 4-chloro acetoacetate new biheterocyclic compound was obtained via ring transformation reaction. However, reaction of the betaine with methyl(or ethyl) bromoacetate used as a ${\alpha}$-halo ester, gave, in-stead, S-alkylated quarternary ammonium salt.

• Journal of Microbiology and Biotechnology
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• 제31권2호
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• pp.317-326
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• 2021

Vanillyl alcohol (VA), which is abundant in Vanilla bean, has strong antioxidant activity. However, the use of VA in the food and cosmetics industries is limited, due to its low solubility in emulsion or organic solvents. Meanwhile, medium chain fatty acids and medium chain monoglycerides have antibacterial activity. We synthesized butyric acid vanillyl ester (BAVE) or caprylic acid vanillyl ester (CAVE) from VA with tributyrin or tricaprylin through transesterification reaction using immobilized lipases. BAVE and CAVE scavenged 2,2-diphenyl-1-picrylhydrazyl radicals in organic solvents. In addition, BAVE and CAVE decreased the production rate of conjugated diene and triene in the menhaden oil-in-water emulsion system. While BAVE showed no antibacterial activity, CAVE showed antibacterial activity against food spoilage bacteria, including Bacillus coagulans. In this study, the antibacterial activity of vanillyl ester with medium chain fatty acid was first revealed. Zeta potential measurements confirmed that BAVE and CAVE were inserted into B. coagulans membrane. In addition, the propidium iodide uptake assay and fluorescent microscopy showed that CAVE increased B. coagulans membrane permeability. Therefore, CAVE is expected to play an important role in the food and cosmetics industries as a bi-functional material with both antioxidant and antibacterial activities.

• 한국수산과학회지
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• 제35권6호
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• pp.654-659
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• 2002

다시마 알긴산으로 에스테르 화합물을 캡슐화할 때 에스테르화합물의 잔존량에 영향을 미치는 가공조건을 알아보기 위하여, 에스테르 화합물의 종류, 유화제 첨가비율 및 에스테르 화합물 (내부물질)에 대한 alginates (벽막물질)의 비율을 달리하여 캡슐을 제조하고 제조중에 사용하는 gelling solution ($1 M\;CaCl_2$)과 캡슐의 세척수에 이동되는 에스테르 화합물의 량과 캡슐에 잔존하는 에스테르 화합물의 량을 측정하였다. 에스테르 화합물의 분자량이 커질수록 캡슐에 잔존하는 량이 증가하였고 gelling solu-tion과 세척수에 이동되는 량이 감소하였다. Ethyl caprylate량에 대한 유화제의 첨가 비율이 증가하석도 gelling solution와 세척수에 이동되는 ethyl caprylate의 량은 1.7$\~$$1.8\%$와 2.3$\~$$6.5\%$이었고 캡슬에 잔존하는 량은 $90.4\~96.0\%$로 거의 변화가 없었다. 그러나 캡슐을 25$^{\circ}C$에 저장할 때 ethyl caprlate의 반감기는 유화제의 첨가비율이 증가할수록 급격히 증가하였다. Ethyl capr빈ate에 대한 alginates 비율이 증가하여도 gelling solution과 세척수에 이동되는 ethyl caprylate 량은 각각 $1.8\~2.0\%$ 및 $2.9\~3.5\%$이었고 캡슐에 잔존하는 량은 $94.3-95.0\%$로 큰 차이가 없었다. 그러나 캡슐을 25$^{\circ}C$에 저장할 때에 벽막물질의 비율이 증가함에 따라 내부물질의 반감기는 증가하였다.

• 공업화학
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• 제25권6호
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• pp.602-606
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• 2014

본 연구에서는 norbornene dialkyl ester 8종을 PVC에 적용하여 물리적 물성의 변화를 관찰하였다. PVC 시편은 PVC와 norbornene dialkyl ester, 안정제 등을 배합하여 제작하였고, 경도, 인장강도, 신율, 인열강도, 투과도, 투명도, 황변지수를 측정하여 DOP를 적용한 경우와 비교하였다. 경도는 dicyclohexyl-5-norbornene-2,3-dicarboxylate (DCHN)를 제외한 화합물 7종이 DOP와 동등 이상의 값을 나타내었다. DCHN을 적용한 경우 경도가 매우 높아 인장 특성 및 인열강도를 분석하지 못하였다. 인장 특성은 diisononyl-5-norbornene-2,3-dicarboxylate (DINN)을 제외한 6종의 화합물이 인장강도와 신율이 모두 개선되는 결과를 나타내었다. 인열강도와 투과도는 측정된 모든 화합물이 DOP를 적용한 경우와 동등 이상의 물성을 보였으며, 투명도는 DDN을 제외한 다른 norbornene 유도체들은 양호한 상태를 나타내었다. 황변지수에서는 DPN과 DON이 DOP와 유사한 결과를 나타내었다.

• 미생물학회지
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• 제33권3호
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• pp.181-186
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• 1997

유기용매계에서 lipase AK를 사용하여 당 ester화합물을 합성하였다. 유기용매로는 당의 용해도가 높고 반응성이 뛰어난 pyridine을, acyl donor로는 vinyl butyrate을 선택하였다. Transesterification반응에 의해 생성된 monobutyryl fructose와 dibutyryl fructose는 TLC 및 GC 분석으로 확인하였다. Transesterification에 미치는 반응조건은 fructose:vinyl butyrate의 비가 1:10(M/M), 반응온도 40^{\circ}C.$, 교반속도 150rpm, 효소량 10mg/ml의 경우가 적당하였으며 반응시간이 길어질수록 전환율이 높아져, 반응 10일 정도에서 전환율은 90% 이상에 도달하였다. 이때 반응 초기에는 monobutyryl fructose가 주로 합성되었으나 시간이 경과함에 따라 dibutyryl fructose의 함량비가 증가하였다. 반응계에 소량의 수분을 첨가하였을 경우에는 반응속도가 감소함과 동시에 반응산물중 dibutyryl fructose의 양은 줄어들고 monobutyryl fructose의 생성량이 증가하는 경향을 보여주었으며, 수분함량 1%에서는 monobutyryl fructose만이 생성되었다.

• 약학회지
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• 제18권2호
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• pp.103-113
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• 1974