• Title/Summary/Keyword: T3T-dimethyl

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Uptake of the Fresh and Aged Residues of Carbofuran by Rice Plants from Soil (침투성(浸透性) 살충제(殺蟲劑) Carbofuran 토양(土壤) 잔류물(殘留物)의 벼에 의(依)한 흡수(吸收))

  • Lee, Jae-Koo;Kyung, Kee-Sung;Wheeler, W.B.
    • Korean Journal of Environmental Agriculture
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    • v.8 no.2
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    • pp.103-118
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    • 1989
  • In order to investigate the uptake of the systemic insecticide, carbofuran, 2,3-dihydro-2,2-dimethyl-7-benzofuranyl-N-methyl(arbamate) residues, fresh and aged, by rice plants, they were grown for 42 days in soils containing freshly treated (T-1), 3-month-aged (T-2), and 6-month-aged residues (T-3). The amounts of $^{14}CO_2$ evolved from $^{14}C-carbofuran$ during the 3-and 6-month aging in soil (temp. $22{\pm}1^{\circ}C$ ; moisture, 50% of the maximum water-holding capacity) were 8.9 and 26.7% of the original radioactivity applied, respectively. Mineralization of $^{14}C-carbofuran$ in soil to $^{14}CO_2$ during 42 days of rice growing was 4.4% (T-1), 11.0% (T-2), and 15.7 (T-3). The methanol extract of the 3-and 6-month-aged soils revealed that 3-keto carbofuran phenol (2,3-dihydro-2,2-dimethyl-3-oxo-7-benzofuranol) was the major metabolite, where as 3-hydroxy carbofuran (2,3-dihydro-2,2-dimethyl-3-hydroxy-7-benzofuranyl-N-methylcarbamate) turned out to be the major metabolite in the shoots by the enzymatic cleavage of the possible conjugate present in the methanol extract. Volatilization of $^{14}C-carbofuran$ in soil during 3-and 6-month-aging, and 42 days of rice growing was 0.026, 0.05, and 0.012-0.018% of the applied radioactivity, respectively. The $^{14}C-radioactivity$ which was absorbed from the soils by rice plants during 42 days of the growing period and persisted in rice plant tissues was 26.8, 21.4, and 10.3% in T-1, T-2, and T-3, respectively. The non-extractable bound residues were 8.3, 37.9, and 54.6% of the originally applied carbofuran in T-1. T-2, and T-3, respectively. The small translocation of $^{14}C-radioactivity$ in T-3 upwards suggests that major metabolite 3-keto carbofuran phenol is conjugated in roots and the low recovery in T-1 indicates the loss of carbofuran from the shoots.

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Photoreaction of 1,4-Diphenyl-1,3-butadiyne and 1,4-Di-t-butyl-1,3-butadiyne with Some Olefins

  • Shim, Sang-Chul;Kim, Sung-Sik
    • Bulletin of the Korean Chemical Society
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    • v.6 no.3
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    • pp.153-157
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    • 1985
  • A diacetylene compound, 1,4-diphenyl-1,3-butadiyne, was photolyzed with 2,3-dimethyl-2-butene, 1,4-cyclohexadiene, dimethyl fumarate, and methyl crotonate, as a model reaction of the phototoxic conjugated polyynes with DNA or RNA and [2 + 2] photocycloadducts were obtained except for 1,4-cyclohexadiene. In the photoreaction of 1,4-diphenyl-1,3-butadiyne with 2,3-dimethyl-2-butene, a [2 + 2 + 2] photoadduct was additionally obtained. The photolysis of 1,4-di-t-buyl-1,3-butadiyne with 2,3-dimethyl-2-butene also yielded a [2 + 2] photoadduct. Fluorescence was observed from all the photoadducts while the reactants did not show any fluorescence.

Generation and Reactivities of Silaethene $Cl_2Si=CHCH_{2}^{t}Bu$-Unsaturated Compounds of 14 group Elements (Ⅸ) (실라에텐 $Cl_2Si=CHCH_{2}^{t}Bu$의 생성과 반응성)

  • Chung-Kyun Kim;Eunmi Park;Mi-Young Ku;Kyungglae Park;Byung-Yun Son
    • Journal of the Korean Chemical Society
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    • v.37 no.2
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    • pp.220-227
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    • 1993
  • Silaethene $Cl_2$Si=$CHCH_2^tBu$, generated as a metastable reaction intermediate by the thermal eliminatio of LiCl from lithiated compound $Cl_2$Si=$CHCH_2^tBu$, react with propene, 2-methylpropene, 1,3-butadiene, 2,3-dimethyl-1,3-butadiene, and anthracene to give ene-reaction product, 2+2-, and 2+4-cycloadducts. They are isolated by vacuum fractional distillation method and spectroscopically identified.

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RNase Resistant RNA in the Egg of Xenopus laevis: I. RNA Extraction and in Vitro Labeling

  • Chung, Hae-Moon
    • The Korean Journal of Zoology
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    • v.20 no.1
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    • pp.9-18
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    • 1977
  • RNA was extracted from the eggs of Xenopus laevis to do preliminary experiments before testing the possibility that if RNase resistant RNA molecules exist in the amphibian egg. Chromatography on Sephadex G-100 column indicated 3 peaks consistently. Only high molecular weight RNA species eluted in the first peak were labeled in vitro using $^{3}H$-dimethyl sulfate to eliminate the possible contribution of base paired oligonucleotides from tRNA. By this method, high specific activity could be obtained and the attached methyl groups were quite stable.

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Measurement of odor compounds from odorous emissions source of Industrial Complex (산업단지에서 배출되는 악취원인물질의 규명)

  • An Sang-Young;Choi Sung-Woo
    • Journal of Environmental Science International
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    • v.14 no.1
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    • pp.81-89
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    • 2005
  • As a typical example of simultaneous analysis of the odorous compounds, the volatile organic compounds from inventory sources in Seongseo industrial area were concentrated and analyzed with thermal desorber/GC/MSD, and major malodorous compounds were estimated. Odor intensity and odor concentration was analyzed simultaneously During a period from November in 2002 to December in 2003, this study was conducted to evaluate malodor emission characterization in major treatment facilities. The major components were Dimethyl sulfide, Dimethyl disulfide, Methyl mercaptane, Ammonia, Benzene, Toluene, m,p-xylene, o-xylene, Styrene, 1,2,4­T.M.B and 1,3,5-T.M.B. Among the six major inventory sources, the odor unit concentration of Night-soil disposal facilities was the highest, $669\~2344\;ou/m^{3}.$

Volatile Flavor Components of Cultivated Radish (Raphanus sativus L.) Sprout (재배한 무순의 향미성분)

  • 송미란
    • The Korean Journal of Food And Nutrition
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    • v.14 no.1
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    • pp.20-27
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    • 2001
  • The consumption of radish ( Rhaphanus sativus L.) sprout, which is Cruciferae family, is increasing because of its pungent flavor and taste. Its volatile components were analyzed by SDE (simultaneous steam distillation & extraction) method and P&T(purge & cryogenic trapping) method. As a solvent, diethyl ether and diethyl ether : pentane mixture(2:1, v/v) were used in SDE method, and diethyl ether in P&T method. Analyzing by GC and GC-MS, the major component was sulfur compounds (19 species, peak area 76.6%) with diethyl ether, sulfur compounds(15. 44.0%) and hydrocarbons(23, 23.8%) with diethyl ether-pentane mixture in SDE method. Also, hydrocarbons(25, 84.1% ) was major component in P& T method. The major volatile component of fresh radish sprout were n-heptane, methyl pentane and that of boiled radish sprout were 4-methylthio-3-butenyl isothiocyanate, methyl mercaptane, 2,3-dimethyl disulfide. Low molecular volatile components were detected more by P& T method, but types and relative quantities of volatile components were measured less comparing to SDE method.

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Syntheses of Alternating Head-to-Head Copolymers of Vinyl Ketones and Vinyl Ethers, and Their Properties. Ring-Opening Polymerization of 2,3,6-Trisubstituted-3,4-dihydro-2H-pyrans

  • Lee, Ju-Yeon;Cho, I-Whan
    • Bulletin of the Korean Chemical Society
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    • v.8 no.2
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    • pp.102-105
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    • 1987
  • 2-Methoxy-6-methyl-3,4-dihydro-2H-pyran ($1_a$), 2-ethoxy-3,6-dimethyl-3,4-dihydro-2H-pyran ($1_b$), and 2-ethoxy-3-methyl-6-ethyl-3,4-dihydro-2H-pyran ($1_c$) were prepared by (4 + 2) cycloaddition reaction from the corresponding vinyl ketones and alkyl vinyl ethers. Compounds $1_{a-c}$ were ring-open polymerized by cationic catalyst to obtain alternating head-to-head (H-H) copolymers. For comparison, copolymer of head-to-tail (H-T) was also prepared by free radical copolymerization of the mixture of the corresponding monomers. The H-H copolymer exhibited some differences in its $^1H$ NMR and IR spectra. However, significant differences were showed between the H-H and H-T copolymers in the $^{13}C$ NMR spectra. Also noteworthy was that$T_g$ value of H-H copolymer was higher than that of the corresponding H-T structure. Decomposition temperature of the H-H copolymer was lower than that of the H-T copolymer. All the H-H and H-T copolymers were soluble in common solvents.

Changes in Essential Oil Contents of Acanthopanax senticosus Harms Grafted on Acanthopanax senticosus var. subinermis Harms (가시오갈피와 좀가시오갈피 접목시 정유성분 변화)

  • Shin, Kuk-Hyun;Cho, Sun-Haeng;Lim, Soon-Sung;Lee, Sang-Hyun;Ryu, Na-Ma;Joo, Wha-Kyun
    • Korean Journal of Medicinal Crop Science
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    • v.6 no.2
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    • pp.114-120
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    • 1998
  • The present study was carried out to investigate the changes in essential oil contents as a part of searching the changes in active components in the graft cultivation of A. senticosus. To increase the yield of aerial parts and the contents of active components of Acanthopanax senticosus, scions of A. senticosus were grafted on different rootstocks. As a result, the contents of calarene, ${\alpha}-beramotene$ and spathulenol increased, but cis-caryophyllene and epizonarene contents decreased. ${\beta}-pinene$, ${\beta}-myrcene$, 2,5,5 -trimethyl-1, 3, 6-heptatriene and ${\beta}-elemene$ were not detected in the leaves of grafted A. senticosus. Essential oils from stems did not differ with the methods of cultivation. Oil contents of 3-year-old plants were higher than those of 1-year-old plants, whereas ${\alpha}-bergamotene$ content(27%) was highest in the stem of grafted A. senticosus(27%). Ethylbenzene, 2-furancarboxaldehyde, M134 $(t_R=2.11)$ and M205 $(t_R=3.16)$ disappeared in the roots of A. senticosus var. subinermis, but 6,6-dimethyl-3-methylenebicycloheptane, M166 $(t_R=1.82)$, and (+) -aromadendrene and ${\beta}-bisabolene$ were newly found.

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Conformations of 25,27-Diacyloxy-26,28-dialkyloxycalix[4]arenes

  • Kwanghyun No;Hee Jung Koo;Min Seong Lee
    • Bulletin of the Korean Chemical Society
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    • v.15 no.9
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    • pp.791-795
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    • 1994
  • 1,3-Dimethyl and dipropyl ethers of p-t-butylcalix[4]arene and calix[4]arenes have been converted to the corresponding diesters, acetate and propionate, and their conformations are inferred based on the $^1H$ and $^{13}C$ NMR spectra. The presence of t-butyl groups is effective in maintaining the cone conformation on derivatization.