• 제목/요약/키워드: Phenol compounds

검색결과 513건 처리시간 0.03초

고추 Oleoresin의 가열조리중 휘발성 성분 및 Capsaicin의 변화 (Changes in Volatile Components and Capsaicin of Oleoresin Red Pepper during Cooking)

  • 최옥수;하봉석
    • 한국식품영양과학회지
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    • 제23권2호
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    • pp.232-237
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    • 1994
  • 건조 고추를 100mesh의 입자이하로 분쇄하여 먼저 감압증류시켜 정유성분을 추출하고, 다시 3배량의 ethyl alcohol을 가하여 $25^{\circ}C$에서 3시간 동안 진탕 추출후 여과, 농축시켜 정유성분을 합하였다. 여기에 같은양의 물과 유화제를 첨가하여 유화시킨 고추 oleoresin을 고온에서 가열조리 중 일어나는 휘발성성분 및 capsaicin의 변화를 검토하였다. 고추 및 고추 oleoresin-의 휘발성 성분은 119성분이 분리되어 그중 35성분이 동정되었다. 2-methoxy-phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-phenol, 1,4-dimethylbenzene, 1,2-benzenedicarboxylic acid, 2-methoxy-4-methylphenol, 4-ethyl-2-methoxy-pheonl 및 5-methyl-2-furancarboxaldehyde 등이 주요 향기 성분이었으며, 시료로부터 oleoresin으로의 이행율은 저분자에서의 휘발성성분의 경우는 매우 낮았다. 온도 100^{\circ}C$에서 3시간 가열조리 후 휘발성 성분은 93성분이 분리되었고 $150^{\circ}C$ 가열조리의 경우는 82성분만 분리되었다. 가열조리 중 휘발성 성분의 소실은 극심하였으며 가열온도가 높을수록 더욱 심하였다. 100^{\circ}C$에서 가열한 경우 상당량이 가열조리 중 소실되었으며 잔존율은 각각의 휘발성 성부넹 크게 달랐다. 특히 nonanoic acid, 2-(1,1-dimethylethyl)-phenol, pentadecane, 1,2-benzenedic-arboxylic acid 등은 70% 이상의 높은 잔존율을 보였고, 1-methyl-1H-pyrrole, 1-(2-furanyl)-ethanone, 2,4-dimethyl-pheonl, d-fenchyl alcohol 및 4-ethyl-2-methoxy-phenol 성분은 검출되지 않았다. 또한 $150^{\circ}C$에서 가열시킨 고추 oleoresin의 휘발성 성분은 $100^{\circ}C$ 보다도 상대적인 잔존율이 더욱 낮았다. Nonanoic acid와 1,2-benzenedicarboxylic acid만 70% 이상의 잔존율을 보였고, 30% 이하의 잔존율을 나타낸 성분으로서는 2-furancarboxaldehyde, 5-methyl-2-furancarboxdldehyde, 1,4-dimethylbenzene, 2,3-diethyl-2-cyclopenten-1-one, 1H-indole 및 9,12-octadecadienoic acid였다. 그리고 $100^{\circ}C$ 가열에서의 미검출성분과 흔적량을 보이던 2-methyl-2=cyclopenten 및 octanoic acid은 검출되지 않았다. 가열조리 중 capsaicin은 비교적 열에 안정하여 대기하의 $100^{\circ}C\;및\;150^{\circ}C$에서 5시간 가열조리 후 잔존율은 각각 84.7% 및 73.3%였고, 질소가스 통기하에서는 잔존율이 88.9% 및 81.8%로 더욱 안정하였다.

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Formamidine류의 합성 및 살균성 (Studies on the synthesis and bactericidal activity of formamidines)

  • 이계주;장반섭
    • 약학회지
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    • 제17권1호
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    • pp.17-20
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    • 1973
  • Six novel compounds of N,N-dimethyl-N'-(6-substituted-2-benzothiazolyl) formamidines nad six novel compounds of N, N-dimethyl-N'-(substituted-phenyl)formamidines were synthesized. They were evaluated fro their bactericidal activities aginst Salmonella typhoso, Escherichia coli, Vibrio cholera, Staphyloccus aureus, Sarcina lutea and for their fungicidal activities against Saccharomyces cereviseae, Candida albicans. It was found that these compounds were considerably more active than phenol, especially against Vibrio cholera, and N, N-dimethy-N'-(4-methyl-phenyl_formamkidine, N, N-dimethyl-N'-(2-methyl-4-bromo-phenyl)formanidine showed most potent bactericidal activities.

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Phenolic Compounds Content and Antioxidant Activity of Rumex crispus Fractions

  • Lee, Kyoung-Min;Jeong, Gwi-Taek;Park, Don-Hee
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2005년도 생물공학의 동향(XVI)
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    • pp.264-267
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    • 2005
  • The purpose of this study was to investigate the ultra sonic extraction method of phenolic compounds and antioxidant activity from Rumex crispus. Rumex crispus was fractionated with hexane, ethyl acetate, butanol and water. The amount of phenol compounds and antioxidant activity was presented higher content in ethyl acetate fraction then others.

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부재료 첨가에 따른 별미장의 향기특성 (Aroma Characteristics of Byeolmijang with Optional Ingredients)

  • 우관식;한서영;윤향식;이준수;정헌상;김행란
    • 한국식품영양과학회지
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    • 제35권6호
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    • pp.738-746
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    • 2006
  • 생황장에 양파를 첨가하였을 때와 무장과 비지장에 표고버섯을 첨가하였을 때, 그리고 찌금장에 다시마를 첨가하였을 때 휘발성 성분을 추출하여 분석 동정하였다. 생황장은 furfural, benzeneacetaldehyde, n-hexadecanoic acid 등이 많이 검출되었고 양파 첨가구에서 1-hexanol, 2,5-dimethylthiophene은 숙성 4일 후에 각각 0.07, 0.11 ppm이 검출되었다. 생황장은 발효 4일된 시료에서 향기성분의 함량이 비교적 높게 나타났으며, n-hexadecanoic acid의 경우 발효 4일된 시료는 발효초기 함량보다 10배 이상 높게 나타났다. 무장에서의 1H-indole과 phenol은 발효초기에는 대조구에서 각각 130.02, 85.38 ppm이었고, 6일째에는 각각 129.68, 95.99 ppm이었다. 표고버섯 첨가 시 1H-indole은 각각 121.90 ppm에서 114.44 ppm으로, phenol은 각각 87.48 ppm에서 75.64 ppm으로 감소하였다. 3-Allyl-6-methoxyphenol, ${\gamma}-dodecalactone$ 등은 대조구에서 검출이 되었으며, 1,2,4-trithiolane, 2-buthyl-2-octenal은 표고버섯 첨가구에서 검출되었다. 비지장에서는 2,4-decadienal이 대조구는 발효초기에는 2.76 ppm, 발효 1일에는 6.46 ppm, 2일에는 5.02 ppm이 검출되었고 표고버섯 첨가구는 발효초기에는 2.92 ppm, 발효 1일에는 3.84 ppm, 2일에는 3.60 ppm이 검출되어 표고버섯 첨가시 함량이 감소하는 것으로 나타났다. Furfural은 증가하는 경향을 보였고, 1,2,4-trithiolane과 lenthionine은 표고버섯 첨가한 시료에서만 검출되었다. 찌금장은 tetramethylpyrazine, hexadecanal, tetradecanoic acid methyl ester, n-hexadecanoic acid, linoleic acid dthyl ester 등이 검출되었고 발효가 진행되어도 이들 성분의 변화는 적었지만, linoleic acid ethyl ester는 감소하였다. 전체적으로 부재료를 첨가하였을 경우에 장 특유의 이취로 알려진 pyrazine류나 hexadecanoic acid 등의 지방산의 함량이 감소하는 것으로 나타났다.

Seibel 포도즙 알코올 발효 및 저장 중 휘발성 향기성분의 변화 (Changes of Volatile Flavor Compounds of Seibel Grape Must during Alcohol Fermentation and Aging)

  • 고경희;장우영
    • 한국미생물·생명공학회지
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    • 제27권6호
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    • pp.491-499
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    • 1999
  • A great variety of the volatile metabolic by-products was formed in yeast cell during alcohol fermentation. The seibel grape (Vitis labrasca) which was grown in the Southern Korea used for wines. The objective of this research was to identify the volatile flavor compounds during alcohol fermentation and aging at 12$^{\circ}C$. saccharomyces cerevisiae and Schizosaccharomyces pombe were inoculated and fermented in seibel grape must. The volatile flavor compounds of logarithmic, stationary and death phases were extracted, concentrated and identified by gas chromatography/mass spectrometer (GC/MS). The volatile flavor compounds were determined by a Hewlett-Packard 5890 II Plus GC which was equipped with Supelcowax 10 fused silica capillary column (60m$\times$0.32mm$\times$0.25${\mu}{\textrm}{m}$ film thickness) wall coated with polyethyleneglycerol. The scan detection method allowed the comparison of the spectrum from the chromatogram of volatile flavor compounds to those in data Wileynbs base library. Among the volatile compounds collected by ether-hexane extraction method, the evolution of 20 main compounds, such as 9 esters (ethyl butyrate, isoamyl acetate, ethyl caproate, n-hexyl acetate, ethl caprylate, ethyl caprate, diethy succinate, ethyl hexadecanoate, 2-pheneethyl acetate), 4 alcohols (3-methyl-1-butanol, 1-hexanol, 1-heptanol, benzoethanol), 4 ketones and acids (2-octanone, caproic acid, caprylic acid, capric acid), 2 furan and phenol (2,6-bis(1,1-dimethyl ethyl)phenol, 2,3-dihydrobenzofuran) were observed during alcohol fermentation and aging. The production of the esters during alcohol fermentation with S. cerevisiae was higher than those of Sch. pombe. The sensory scores of the aged wine samples in aroma, taste and overall acceptability were not significantly different(p<0.05).

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Comparative phenolic compound profiles and antioxidative activity of the fruit, leaves, and roots of Korean ginseng (Panax ginseng Meyer) according to cultivation years

  • Chung, Ill-Min;Lim, Ju-Jin;Ahn, Mun-Seob;Jeong, Haet-Nim;An, Tae-Jin;Kim, Seung-Hyun
    • Journal of Ginseng Research
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    • 제40권1호
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    • pp.68-75
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    • 2016
  • Background: The study of phenolic compounds profiles and antioxidative activity in ginseng fruit, leaves, and roots with respect to cultivation years, and has been little reported to date. Hence, this study examined the phenolic compounds profiles and 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free-radical-scavenging activities in the fruit, leaves, and roots of Korean ginseng (Panax ginseng Meyer) as a function of cultivation year. Methods: Profiling of 23 phenolic compounds in ginseng fruit, leaves, and roots was investigated using ultra-high performance liquid chromatography with the external calibration method. Antioxidative activity of ginseng fruit, leaves, and roots were evaluated using the method of DPPH free-radical-scavenging activity. Results: The total phenol content in ginseng fruit and leaves was higher than in ginseng roots (p < 0.05), and the phenol content in the ginseng samples was significantly correlated to the DPPH free-radical-scavenging activity ($r=0.928^{****}$). In particular, p-coumaric acid ($r=0.847^{****}$) and ferulic acid ($r=0.742^{****}$) greatly affected the DPPH activity. Among the 23 phenolic compounds studied, phenolic acids were more abundant in ginseng fruit, leaves, and roots than the flavonoids and other compounds (p < 0.05). In particular, chlorogenic acid, gentisic acid, p- and m-coumaric acid, and rutin were the major phenolic compounds in 3e6-yr-old ginseng fruit, leaves, and roots. Conclusion: This study provides basic information about the antioxidative activity and phenolic compounds profiles in fruit, leaves, and roots of Korean ginseng with cultivation years. This information is potentially useful to ginseng growers and industries involved in the production of high-quality and nutritional ginseng products.

GAC를 이용한 RSTA에서 Phenol과 4-Nitrophenol의 이성분계 경쟁흡착 (Competitive Adsorption for Binary Mixture of 4-Nitrophenol and Phenol on RSTA using GAC)

  • 이승목;김대현
    • 대한환경공학회지
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    • 제22권4호
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    • pp.723-731
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    • 2000
  • 유해유기화합물질 처리시 처리효율을 증대시키기 위하여, 본 연구에서는 GAC를 이용한 RSTA에서 phenol과 4-nitrophenol 의 경쟁흡착을 연구하였다. 이성분계 흡착등온시 phenol은 Freundlich 흡착동온식 적용이 불가능하였다. 그리고 활성탄 주입량이 적어짐에 따라 또 흡착질의 농도가 증가함에 따라 두 성분간의 경쟁흡착은 심화되었다. RSTA를 이용한 연속식 실힘에서는 유입유량이 감소할수록 두 성분간의 경쟁흡착성향은 증가하는 것으로 나타났다. 수축 각 변화에 따른 경쟁흡착실험에서는 수축각이 커질수록 파과시간이 증가하였으며, 활성탄 충전층 수를 변화시킨 실험에서는 충전층 수를 증가시킴에 따라 각 성분의 흡착효율 및 phenol에 대한 4-nitrophenol 경쟁흡착능은 증가하였다. RSTA에서의 이러한 성능 증대는 유체의 정제와 분리에 적용할 수 있을 것이다.

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남강의 수중보에서 발생하는 이취미 물질에 관한 연구 (A Study on Odor and Taste from Nam River)

  • 이춘식;박현건
    • 한국환경과학회지
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    • 제11권4호
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    • pp.399-403
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    • 2002
  • This study was designed to analyse the odor from Nam river. The characteristic odor in the water occurred from geosmin and phenol, p-cresol and indol were detected from sediment/water samples. The others were detected as alcohols and fat acid compounds. Algae causing odor and taste were identified as Oscillatoria sp. and Synedra acus. 15 species of phytoplankton, a zooplankton, an eelworm and chironomus were identified in water/sediment sample.

Efficient Ultrasound Enhance Novel Series of 2-((E)-2,3-Dihydro-2-(4-(phenylthio)phenyl)benzo[b][1,4]thiazepin-4-yl)phenol as an Antimicrobial Agent

  • Chate, Asha V.;Joshi, Ratnadeep S.;Badadhe, Pravin V.;Dabhade, Sanjay K.;Gill, Charansingh H.
    • Bulletin of the Korean Chemical Society
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    • 제32권11호
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    • pp.3887-3892
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    • 2011
  • An efficient synthesis of 1,5-Benzothiazepines via Michael addition of corresponding (E)-1-(2-hydroxyphenyl)-3-(4-(phenylthio)phenyl)prop-2-en-1-one is described under ultrasound irradiation. A series of novel 2-((E)-2,3-dihydro-2-(4-(phenylthio)phenyl)benzo[b][1,4]thiazepin-4-yl)phenol derivatives was confirmed on the basis of $^1H$ NMR, Mass, IR spectral data and Elemental analysis. The synthesized compounds were evaluated for their antimicrobial activities. Most of the compounds were found to be comparable potent than the reference standard drugs. Utilization of ultrasound irradiation, simple reaction conditions, isolation, and purification makes this manipulation very interesting from an economic and environmental perspective.

Redoxcitrinin, a Biogenetic Precursor of Citrinin from Marine Isolate of Fungus Penicillium sp.

  • Zhang, Dahai;Li, Xianguo;Kang, Jung-Sook;Choi, Hong-Dae;Jung, Jee-H.;Son, Byeng-Wha
    • Journal of Microbiology and Biotechnology
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    • 제17권5호
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    • pp.865-867
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    • 2007
  • A chemical analysis of the fermentation of the marine-derived fungus Penicillium sp. led to the isolation of a biogenetic precursor of citrinin, redoxcitrinin(1), together with polyketide mycotoxins, phenol A(2), citrinin H2(3), 4-hydroxymellein(4), citrinin(5), and phenol A acid(6). The structures of compounds 1-6 were determined on the basis of physicochemical data analyses. Among them, compounds 1-3 exhibited a potent radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl(DPPH) with $IC_{50}$ values of 27.7, 23.4, and $27.2{\mu}M$, respectively.