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
  • [41] SYNTHESIS OF PROLYL ENDOPEPTIDASE INHIBITORS AND EVALUATION OF THEIR STRUCTURE-ACTIVITY-RELATIONSHIPS - IN-VITRO INHIBITION OF PROLYL ENDOPEPTIDASE FROM CANINE BRAIN
    ARAI, H
    NISHIOKA, H
    NIWA, S
    YAMANAKA, T
    TANAKA, Y
    YOSHINAGA, K
    KOBAYASHI, N
    MIURA, N
    IKEDA, Y
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1993, 41 (09) : 1583 - 1588
  • [42] Synthetic lipopeptide adjuvants and Toll-like receptor 2 -: structure-activity relationships
    Spohn, R
    Buwitt-Beckmann, U
    Brock, R
    Jung, G
    Ulmer, AJ
    Wiesmüller, KH
    VACCINE, 2004, 22 (19) : 2494 - 2499
  • [43] RENIN INHIBITORS .2. SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF N-TERMINUS MODIFIED INHIBITORS CONTAINING A HOMOSTATINE ANALOG
    ATSUUMI, S
    NAKANO, M
    KOIKE, Y
    TANAKA, S
    FUNABASHI, H
    MATSUYAMA, K
    NAKANO, M
    SAWASAKI, Y
    FUNABASHI, K
    MORISHIMA, H
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (12) : 3214 - 3221
  • [44] SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NEW (5R,8R,10R)-ERGOLINE DERIVATIVES WITH ANTIHYPERTENSIVE OR DOPAMINERGIC ACTIVITY
    OHNO, S
    ADACHI, Y
    KOUMORI, M
    MIZUKOSHI, K
    NAGASAKA, M
    ICHIHARA, K
    KATO, E
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1994, 42 (07) : 1463 - 1473
  • [45] STRUCTURE-ACTIVITY-RELATIONSHIPS OF EPOXIDES - INDUCTION OF SISTER-CHROMATID EXCHANGES IN CHINESE-HAMSTER V79 CELLS
    VONDERHUDE, W
    CARSTENSEN, S
    OBE, G
    MUTATION RESEARCH, 1991, 249 (01): : 55 - 70
  • [46] Investigation on the substitution effects of the flavonoids as potent anticancer agents: a structure-activity relationships study
    Wang, Xiao-Bing
    Liu, Wei
    Yang, Lei
    Guo, Qing-Long
    Kong, Ling-Yi
    MEDICINAL CHEMISTRY RESEARCH, 2012, 21 (08) : 1833 - 1849
  • [47] Synthesis and structure-activity relationships of asymmetric dimeric β-carboline derivatives as potential antitumor agents
    Guo, Liang
    Chen, Wei
    Cao, Rihui
    Fan, Wenxi
    Ma, Qin
    Zhang, Jie
    Dai, Bin
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 147 : 253 - 265
  • [48] Synthesis and structure-activity relationships of TAN-1511 analogues as potent hematopoietic agents
    Itoh, F
    Nishikimi, Y
    Hasuoka, A
    Yoshioka, Y
    Yukishige, K
    Tanida, S
    Aono, T
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1998, 46 (02) : 255 - 273
  • [49] SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NEW (5R,8S,10R)-ERGOLINE DERIVATIVES WITH ANTIHYPERTENSIVE OR DOPAMINERGIC ACTIVITY
    OHNO, S
    KOUMORI, M
    ADACHI, Y
    MIZUKOSHI, K
    NAGASAKA, M
    ICHIHARA, K
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1994, 42 (10) : 2042 - 2048
  • [50] Structure-activity relationships of naturally occurring and synthetic opioid tetrapeptides acting on locus coeruleus neurons
    Yang, YR
    Chiu, TH
    Chen, CL
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 372 (03) : 229 - 236