• Title/Summary/Keyword: carboxylic acid

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Sulfonation of Polyamide Containing Carboxylic Acid (Carboxylic acid를 함유한 sulfonated polynmide의 제조)

  • Jeon, Jong-Young;Lee, Gi-Jo
    • Journal of Sericultural and Entomological Science
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    • v.48 no.1
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    • pp.1-5
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    • 2006
  • Polyamide containing carboxylic acid was sulfonated with chlorosulfonic acid in dichloroethane under various conditions. The impact of the sulfonating agent concentration, the reaction temperature, and the reaction time on the ion exchange capacity was investigated. The mechanical and thermal properties, the contact angle, and the change of poly-dispersity were calculated for studying change of their properties. The reactions were effective, when the temperature was below $10^{\circ}C$ and the concentration of chlorosulfonic acid was below 0.05 mol. The value of ion exchange capacity was increased with reaction time. Thermal and mechanical properties were nearly unchanged according to the degree of sulfonation, but the contact angle was increased with increasing the value of ion exchange capacity.

Conformation of Retinoic Acid and Structure-Activity Relationships -Retinobenzoic Acid- (레티노익 산의 형태와 구조-활성 관계 -레티노벤조익 산-)

  • Rhee, Jong-Dal;Rhee, In-Ja
    • YAKHAK HOEJI
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    • v.38 no.3
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    • pp.230-237
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    • 1994
  • The structure-activity relationships of (E)-chalcone-4-carboxylic acids, flavone-4'-carboxylic acids, two types of aromatic amides, terephthalic monoanilides, and (arylcarboxamido)benzoic acids, which were made by Shudo group, are discussed by conformation analysis(AM1) of retinoic acid and those compounds. Conformer of each compound is superimposed on the conformationally restricted compound, 4-(6,7,8,9-tetrahydro-6,6,9,9-tetramethyl-4H-4-oxonaphto[ 2,3-b]pyran-2-yl) benzoic acid(Fv80), possessing the strongest differentiation-inducing activity on human promyelocytic leukemia cells HL-60. The results indicated that the lengths between the carboxylic carbon and the two 6, 9 carbons binding to dimethyl, 1.20 nm and 1.09 nm, as well as the planarity of molecule are very important factors for the activity, especially 1.20 nm. In the case of the recently synthesized azulenic retinoic acids by Sato, et al. in 1993, the distance probably is also important, resulted from superimposing them on a Ch55 conformer and Fv80. The distance 1.0 nm is also important in Ch55. Several conformers of all-trans retinoic acid (RA) are well superimposed on the almost non-flexible Fv80, RA, 9-cis RA, and, specifically s-10,12 cis RA. And a simple hexangular model of RA is suggested to draw RA conformers easily without computer drawing model or molecular model.

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Use of Polycarboxylic Acid to Inhibit Heat-and Moisture-Induced Yellowing of ECF/TCF Bleached Hardwood Kraft Pulp

  • Kawae, Ayano;Uchida, Yosuke
    • Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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    • 2006.06b
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    • pp.331-336
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    • 2006
  • The aim of this work was to inhibit the heat-and moisture-induced yellowing of ECF/TCF bleached hard wood kraft pulp (HBKP) retaining hexenuronic acid (HexA). We have already reported that one of the derivatives of HexA, 5-formyl-2-furancarboxylic acid (FFA), causes yellowing of HBKP in acidic paper, and that FFA might polymerize or react with pulp components to form new chromophoric groups (1). In this study, it was shown that the carboxylic base of FFA interacts with that of glucuronic acid or galacturonic acid, resulting in strong yellowing. Therefore, it seems that preventing the reaction of carboxylic bases could be effective in suppressing this yellowing. We have discovered that polycarboxylic acids (for example, citric acid, tartaric acid, etc.) are useful as a yellowing inhibitor.

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Constituents from the Root of Symplocarpus renifolius Schott (앉은부채(Symplocarpus renifolius Schott) 뿌리의 성분)

  • Youm, Jeong-Rok;Park, Dong-Woo
    • Korean Journal of Pharmacognosy
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    • v.28 no.3
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    • pp.143-148
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    • 1997
  • From the root of Symplocarpus renifolius, four compounds were isolated and their structure was elucidated by chemical and spectroscopic methods. They were identified as ${\beta}-sitosterol$ (compound 1), asparagine (compound 2), isocorydine (compound 3) and 3-hydroxymethyl-4-phenyl phenoxy carboxylic acid glucopyranosyl ester (compound 4). These compounds were firstly isolated from roots of Symplocarpus renifolius. Compound 4 was identified as a new compound, named as symplocarposide.

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Calix[6]arene Bearing Carboxylic Acid and Amide Groups in Polymeric CTA Membrane

  • Kim, Jong-Seung;Lee, Soo-Heon;Yu, Sang-Hyeok;Cho, Moon-Hwan;Kim, Dong-Won;Kwon, Seon-Gil;Lee, Eil-Hee
    • Bulletin of the Korean Chemical Society
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    • v.23 no.8
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    • pp.1085-1088
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    • 2002
  • Calix[6]arene having both carboxylic acid (1,3,5-) and carboxamide (2,4,6-) in an alternative way was synthesized. Transport rates of alkali and alkaline-earth metal ions were tested in bulk liquid membrane and polymer inclusion membrane. Ba2+ ion was found to give the highest transport rate among tested metal ions in both BLM and PIM systems. In PIM system, high durability (longer than 30 days) of the membrane was observed.

Synthesis and In Vitro Cytotoxicity of 1,3-Dioxoindan-2-Carboxylic Acid Arylamides

  • Jung, Jae-Kyung;Ryu, Jin-Hyeong;Yang, Sung-Il;Cho, Jung-Sook;Lee , Hee-Soon
    • Archives of Pharmacal Research
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    • v.27 no.10
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    • pp.997-1000
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    • 2004
  • A series of 1,3-dioxoindan-2-carboxylic acid arylamides were synthesized and evaluated for in vitro cytotoxicity against four human cancer cell lines (HOP62, SK-OV-3, MD-MB-468 and T- 47D). The most active was compound 3e (1.2 ${\mu}M$ against SK-OV-3 cell line) bearing a 4- methyl substituent.

Clean Reduction of $\alpha,\beta$-Unsaturated Carboxylic Acid Derviatives to the Saturated Derivatives by Potassium Triphenylborohydride in the Presence of Phenol

  • Park, Soo-Bong;Kim, Kwan-Eung;Yoon, Nung-Min
    • Bulletin of the Korean Chemical Society
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    • v.9 no.6
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    • pp.352-355
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    • 1988
  • ${\alpha},{\beta}$-unsaturated carboxylic acid derivatives such as esters, amides, and nitriles are readily reduced to the corresponding saturated derivatives by potassium triphenylborohydride, $KPh_3BH$, in the presence of phenol, a quenching agent, in excellent yields.