Structure-Activity-Relationships of Synthetic Organic Tanning Agents

被引:0
作者
Ammenn, Jochen [1 ]
Glocknitzer, Franz [1 ]
Tiarks, Franca
Wolf, Gerhard [1 ]
机构
[1] BASF SE, D-67056 Ludwigshafen, Germany
来源
XXX CONGRESS OF THE INTERNATIONAL UNION OF LEATHER TECHNOLOGISTS & CHEMISTS SOCIETIES, PROCEEDINGS | 2009年
关键词
Syntan; Structure-Activity Relationship; Formaldehyde Condensate; Sulfon;
D O I
暂无
中图分类号
TB3 [工程材料学]; TS1 [纺织工业、染整工业];
学科分类号
0805 ; 080502 ; 0821 ;
摘要
In this paper the structure of various syntans are studied and compared to natural tanning agents. Following structure-property relationships were found in reference to tanning efficiency: - Although many natural tannins contain methoxy groups, we could not positively proof a tanning effect of methoxy groups as such. - The spacer group between the phenol moieties does play a role in tanning. Comparing different spacers the benzyliden spacer proofed to be most beneficial for shrinkage temperature. However based on physicochemical properties (solubility, accessibility) the methylene and sulfon spacer appear more favorable. - Natural tannins frequently contain higher oxidized moieties based on catechol or pyrogallol. Trials showed that their influence on the shrinkage temperature was less pronounced than the effect on lightfastness of the obtained leathers, with the phenol based product giving best lightfastness. - The molecular weight of condensates influences the tanning capacity. We used products of three different molecular weights all containing the sodium salt of phenolsulfonic acid and achieved shrinkage temperatures that differed significantly and increased with molecular weight of the condensate.
引用
收藏
页码:190 / 193
页数:4
相关论文
共 50 条
  • [31] LONG-ACTING DIHYDROPYRIDINE CALCIUM-ANTAGONISTS .9. STRUCTURE-ACTIVITY-RELATIONSHIPS AROUND AMLODIPINE
    ALKER, D
    ARROWSMITH, JE
    CAMPBELL, SF
    CROSS, PE
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1991, 26 (09) : 907 - 913
  • [32] SYNTHESIS, GASTROINTESTINAL PROKINETIC ACTIVITY AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL N-[[2-(DIALKYLAMINO)ETHOXY]BENZYL]BENZAMIDE DERIVATIVES
    SAKAGUCHI, J
    NISHINO, H
    OGAWA, N
    IWANAGA, Y
    YASUDA, S
    KATO, H
    ITO, Y
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (01) : 202 - 211
  • [33] INHIBITORY EFFECT OF PERILLOSIDE-A AND PERILLOSIDE-C, AND RELATED MONOTERPENE GLUCOSIDES ON ALDOSE REDUCTASE AND THEIR STRUCTURE-ACTIVITY-RELATIONSHIPS
    FUJITA, T
    OHIRA, K
    MIYATAKE, K
    NAKANO, Y
    NAKAYAMA, M
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1995, 43 (06) : 920 - 926
  • [34] Structure-activity relationships and optimization of acyclic acylphloroglucinol analogues as novel antimicrobial agents
    Tan, Haibo
    Liu, Hongxin
    Zhao, Liyun
    Yuan, Yao
    Li, Bailin
    Jiang, Yueming
    Gong, Liang
    Qiu, Shengxiang
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 125 : 492 - 499
  • [35] Synthesis and structure-activity relationships of novel benzoxaboroles as a new class of antimalarial agents
    Zhang, Yong-Kang
    Plattner, Jacob J.
    Freund, Yvonne R.
    Easom, Eric E.
    Zhou, Yasheen
    Gut, Jiri
    Rosenthal, Philip J.
    Waterson, David
    Gamo, Francisco-Javier
    Angulo-Barturen, Inigo
    Ge, Min
    Li, Zhiya
    Li, Lingchao
    Jian, Yong
    Cui, Han
    Wang, Hailong
    Yang, Jian
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (02) : 644 - 651
  • [36] GLYCYRRHETINIC ACID-DERIVATIVES AS POTENT INHIBITORS OF NA+, K+-ATPASE - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS
    TERASAWA, T
    OKADA, T
    HARA, T
    ITOH, K
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1992, 27 (04) : 345 - 351
  • [37] Structure-activity relationships and evaluation of esterified diterpenoid alkaloid derivatives as antiproliferative agents
    Wada, Koji
    Goto, Masuo
    Shimizu, Takahiro
    Kusanagi, Nami
    Mizukami, Megumi
    Suzuki, Yuji
    Li, Kang-Po
    Lee, Kuo-Hsiung
    Yamashita, Hiroshi
    JOURNAL OF NATURAL MEDICINES, 2019, 73 (04) : 789 - 799
  • [38] Imidazo- and triazoloquinolones as antibacterial agents. Synthesis and structure-activity relationships
    Fujita, M
    Egawa, H
    Kataoka, M
    Miyamoto, T
    Nakano, J
    Matsumoto, J
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1995, 43 (12) : 2123 - 2132
  • [39] β-Lactams as promising anticancer agents: Molecular hybrids, structure activity relationships and potential targets
    Fu, Dong-Jun
    Zhang, Yun-Feng
    Chang, An-Qi
    Li, Jun
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 201
  • [40] EVOLUTIONARY COMPUTATION FOR REVEAL STRUCTURE-ACTIVITY-RELATIONSHIPS IN 3-PHENOXYCHROMONE AND 3-PHENOXY-4-HYDROXYCOUMARIN DERIVATIVES
    TETKO, IV
    TANCHUK, VY
    VASILEV, SA
    KHILYA, VP
    PODA, GI
    LUIK, AI
    BIOORGANICHESKAYA KHIMIYA, 1995, 21 (10): : 809 - 815