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Journal articles on the topic 'Thiodipropionic'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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1

Adaikalasamy, John K., Selva A. Priya, and Sunaja K. R. Devi. "Kinetic Study on Oxidation of Thiodipropionic Acid by Iron (III)- bipyridine Complex." Mapana - Journal of Sciences 15, no. 2 (2016): 33–44. http://dx.doi.org/10.12723/mjs.37.3.

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Iron(III)-bipyridine complex was prepared andcharacterized by UV-Visible spectrophotometer. Kineticstudy was carried out by using this iron(III)-bipyridinewith thiodipropionic acid in aqueous acetonitrile solution.The reaction was optimized by studying the effect onsubstrate, solvent, oxidant, acidity and temperature. Firstorder, second order rate constants and activationparameters were calculated. The above reaction wasfound to be second order and proceeded through electrontransfer from thiodipropionic acid to iron(III)-bipyridinecomplex. The product was characterized and confirmedby IR and N
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2

Bland, J. A., and M. E. A. Cudby. "Polymorphism of thiodipropionic acid." Journal of Applied Chemistry 12, no. 7 (2007): 320–28. http://dx.doi.org/10.1002/jctb.5010120705.

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3

Wang, Xiao, You Han, Xing Xing Han, Xiangyang Hou, Ji-Jiang Wang, and Feng Fu. "Highly selective and sensitive detection of Hg2+, Cr2O72−, and nitrobenzene/2,4-dinitrophenol in water via two fluorescent Cd-CPs." New Journal of Chemistry 42, no. 24 (2018): 19844–52. http://dx.doi.org/10.1039/c8nj04683b.

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Taking advantage of fluorescent Cd-CPs with 3,3′-thiodipropionic acid and imidazole ligands, herein, we demonstrate the synthesis of functional CPs, and develop two Cd-CP fluorescence sensing materials with highly selective and sensitive detection of Hg<sup>2+</sup>, Cr<sub>2</sub>O<sub>7</sub><sup>2−</sup>, NB,/2,4-DNP in water.
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4

Loubalová, Ivana, and Pavel Kopel. "Coordination Compounds of Cu, Zn, and Ni with Dicarboxylic Acids and N Donor Ligands, and Their Biological Activity: A Review." Molecules 28, no. 3 (2023): 1445. http://dx.doi.org/10.3390/molecules28031445.

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Complexes of carboxylic acids are very often studied due to their interesting structural, spectral, and magnetic properties. This review is focused on complexes of four dicarboxylic acids, namely, 2,2′-thiodioacetic, 3,3′-thiodipropionic, 3,3′-dithiodipropionic, and fumaric acid. Many of the complexes were characterized by single crystal X-ray analyses. Without the analyses, it is very difficult to predict the coordination mode of carboxylate groups or nitrogen ligands on central atoms. Thus, structural properties are also discussed, as well as potential applications.
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5

Lotti, N., L. Finelli, T. Milizia, A. Munari, and P. Manaresi. "Preparation and thermal behavior of random copolyesters of thiodipropionic acid." European Polymer Journal 36, no. 5 (2000): 929–36. http://dx.doi.org/10.1016/s0014-3057(99)00141-x.

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6

Chandra, Sulekh, and Amit Kumar Sharma. "Antifungal and Spectral Studies of Cr(III) and Mn(II) Complexes Derived from 3,3′-Thiodipropionic Acid Derivative." Research Letters in Inorganic Chemistry 2009 (August 23, 2009): 1–4. http://dx.doi.org/10.1155/2009/945670.

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The Cr(III) and Mn(II) complexes with a ligand derived from 3,3′-thiodipropionic acid have been synthesized and characterized by elemental analysis, molar conductance measurements, magnetic susceptibility measurements, IR, UV, and EPR spectral studies. The complexes are found to have [Cr(L)X]X2 and [Mn(L)X]X, compositions, where L = quinquedentate ligand and X=NO3−, Cl− and OAc−. The complexes possess the six coordinated octahedral geometry with monomeric compositions. The evaluated bonding parameters, Aiso and β, account for the covalent type metal-ligand bonding. The fungicidal activity of t
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7

Mohan, Hari. "Intra- and inter-molecular electron transfer reactions in 3,3′-thiodipropionic acid." J. Chem. Soc., Perkin Trans. 2, no. 11 (1990): 1821–24. http://dx.doi.org/10.1039/p29900001821.

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8

Mastragostino, M., L. Meneghello, P. Manaresi, M. C. Bignozzi, F. Pilati, and A. Munari. "Polymer electrolytes based on polyesters of thiodipropionic acid: 2. Electrochemical characterization." Polymer 35, no. 4 (1994): 845–48. http://dx.doi.org/10.1016/0032-3861(94)90884-2.

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9

MOHAN, H. "ChemInform Abstract: Intra- and Intermolecular Electron Transfer Reactions in 3,3′- Thiodipropionic Acid." ChemInform 22, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199108112.

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10

KAJIMOTO, Goro, Hiromi YOSHIDA, and Akira SHIBAHARA. "Effect of Thiodipropionic Acid on the Decomposition of Tocopherol in Oils by Autoxidation." Journal of Japan Oil Chemists' Society 37, no. 4 (1988): 294–98. http://dx.doi.org/10.5650/jos1956.37.294.

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11

Rabaâ, Hassan, Aziz Ennaciri, Thomas R. Cundari, Mohammad A. Omary, and Changming Fang. "Molecular DFT structure and packing effect of thiodipropionic and dithiodiglycolic acids and salts." Journal of Molecular Structure: THEOCHEM 911, no. 1-3 (2009): 52–57. http://dx.doi.org/10.1016/j.theochem.2009.06.038.

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12

Sudhakar, Kosinapogu, and R. Nanthini. "Synthesis, Characterization and Biological Applications of Random Aliphatic Copolythioesters Using 3,3'-Thiodipropionic Acid." Asian Journal of Chemistry 30, no. 1 (2017): 191–94. http://dx.doi.org/10.14233/ajchem.2018.20978.

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13

BORGHINI, C., M. MASTRAGOSTINO, L. MENEGHELLO, P. MANARESI, and A. MUNARI. "Electrochemical characterization of plasticized-polymer electrolyte based on a polyester of thiodipropionic acid." Solid State Ionics 67, no. 3-4 (1994): 263–69. http://dx.doi.org/10.1016/0167-2738(94)90015-9.

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14

Sudhakar, K., and B. Kalpana. "3, 3’-thiodipropionic acid: A versatile monomer to synthesis aliphatic random copolyesters with biological applications." Research Journal of Chemistry and Environment 25, no. 12 (2021): 19–27. http://dx.doi.org/10.25303/2512rjce1927.

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A prime monomer 3,3’-thiodipropionic acid was mixed with other monomers such as 1,4 butanediol and 1,4 butanedioic acid to produce aliphatic random copolyester Poly(butylthiodipropionate-co-butylbu tanedioate) (PBTBB) by direct melt polycondensation method. The physical properties such as solubility by solubility test, inherent viscosity by Ubbelohde viscometer, Tg by differential scanning colorimetry (DSC) and the crystalline nature by X-ray diffraction (XRD) technique of synthesized polymer were investigated. The chemical structure of the obtained copolyester was studied by FTIR, 1H-NMR and
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15

Diamante, Catherine, Monice Zondlo Fiume, Wilma F. Bergfeld, et al. "Final Safety Assessment of Thiodipropionic Acid and Its Dialkyl Esters as Used in Cosmetics." International Journal of Toxicology 29, no. 4_suppl (2010): 137S—150S. http://dx.doi.org/10.1177/1091581810373150.

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Dilauryl thiodipropionate (DLTDP), dicetyl thiodipropionate, dimyristyl thiodipropionate, distearyl thiodipropionate, and ditridecyl thiodipropionate are dialkyl esters of their respective alcohols and thiodipropionic acid (TDPA) used in cosmetics. Ingested DLTDP was excreted in the urine as TDPA. Single-dose acute oral and parenteral studies and subchronic and chronic repeated dose oral studies did not suggest significant toxicity. Neither DLTDP nor TDPA was irritating to animal skin or eyes and they were not sensitizers. TDPA was neither a teratogen nor a reproductive toxicant. Genotoxicity
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16

Heine, Viktoria, Christina Meinert-Berning, Janina Lück, et al. "The catabolism of 3,3’-thiodipropionic acid in Variovorax paradoxus strain TBEA6: A proteomic analysis." PLOS ONE 14, no. 2 (2019): e0211876. http://dx.doi.org/10.1371/journal.pone.0211876.

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17

Kamei, Yasutaka, Atsushi Nagai, Haruo Nishida, Hiroshi Kimura, and Takeshi Endo. "Biosynthesis and Biodegradability of Copolythioesters from 3,3′-Thiodipropionic Acid and Plant Oils byCupriviadus necator." Macromolecular Bioscience 7, no. 3 (2007): 364–72. http://dx.doi.org/10.1002/mabi.200600239.

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18

Bandiera, M., P. Manaresi, A. Munari, M. C. Borghini, and M. Mastragostino. "Effect of sodium sulfonate groups on the ionic conductivity of a copolyester of thiodipropionic acid." European Polymer Journal 33, no. 10-12 (1997): 1679–83. http://dx.doi.org/10.1016/s0014-3057(97)00036-0.

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19

Manaresi, P., M. C. Bignozzi, F. Pilati, et al. "Polymer electrolytes based on polyesters of thiodipropionic acid: 1. Synthesis, characterization and ionic conductivity measurements." Polymer 34, no. 11 (1993): 2422–26. http://dx.doi.org/10.1016/0032-3861(93)90831-t.

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20

Pournara, Anastasia, Dimitra Kovala-Demertzi, Nikolaos Kourkoumelis, Spyros Georgakopoulos, and Ioannis D. Kostas. "Platinum/3,3´-thiodipropionic acid nanoparticles as recyclable catalysts for the selective hydrogenation of trans-cinnamaldehyde." Catalysis Communications 43 (January 2014): 57–60. http://dx.doi.org/10.1016/j.catcom.2013.09.008.

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21

Ma, Chunlin, Qi Zhu, and Rufen Zhang. "Synthesis and Structural Characterization of Triorganotin(IV) Derivatives with 2,2′-Thiodiglycolic Acid and 3,3′-Thiodipropionic Acid." Journal of Inorganic and Organometallic Polymers and Materials 22, no. 5 (2012): 1206–12. http://dx.doi.org/10.1007/s10904-012-9700-1.

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22

Doberstein, Christina, Jessica Grote, Jan Hendrik Wübbeler, and Alexander Steinbüchel. "Polythioester synthesis in Ralstonia eutropha H16: Novel insights into 3,3′-thiodipropionic acid and 3,3′-dithiodipropionic acid catabolism." Journal of Biotechnology 184 (August 2014): 187–98. http://dx.doi.org/10.1016/j.jbiotec.2014.05.022.

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23

Buchtelova, Hana, Zuzana Skubalova, Vladislav Strmiska, et al. "Synthesis and structural characterization of antimicrobial binuclear copper(II) coordination compounds bridged by hydroxy- and/or thiodipropionic acid." Journal of Inorganic Biochemistry 191 (February 2019): 8–20. http://dx.doi.org/10.1016/j.jinorgbio.2018.10.011.

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24

Calabrese, Joseph P., and Gary K. Bissonnette. "Improved detection of acid mine water stressed coliform bacteria on media containing catalase and sodium pyruvate." Canadian Journal of Microbiology 36, no. 8 (1990): 544–50. http://dx.doi.org/10.1139/m90-095.

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Pure culture suspensions of two strains of exponential and stationary phase Escherichia coli exhibited significant reductions in catalase activity following exposure to acid mine water (AMW). The exogenous addition of catalase (500–2000 U) or sodium pyruvate (0.05–5%) to a nonselective recovery medium resulted in enhanced detection (12- to 465-fold) of AMW-stressed E. coli as compared with recovery on the medium lacking these supplements, whereas addition of 3,3′-thiodipropionic acid failed to improve recovery. Additional in vitro experiments utilizing selective M-FC, mT7, and M-Endo media con
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25

Zhila, Natalia O., Kristina Yu Sapozhnikova, Arina V. Berezovskaya, et al. "Biosynthesis and Properties of Sulfur-Containing Polyhydroxyalkanoates (PHAs) Produced by Wild-Type Strain Cupriavidus necator B-10646." Polymers 15, no. 4 (2023): 1005. http://dx.doi.org/10.3390/polym15041005.

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The study addresses the growth of the wild-type strain Cupriavidus necator B-10646 and the synthesis of sulfur-containing polyhydroxyalkanoates (PHA) by this strain on media containing fructose and three different precursors (3-mercaptopropionic acid, 3′,3′-dithiodipropionic acid and 3′,3′-thiodipropionic acid). By varying the concentration and number of doses of the precursors added into the bacterial culture, it was possible to find conditions that ensure the formation of 3-mercaptopropionate (3MP) monomers from the precursors and their incorporation into the C-chain of poly(3-hydroxybutyrat
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26

KAJIMOTO, Goro, Hiromi YOSHIDA, and Akira SHIBAHARA. "Influence of gallic and thiodipropionic acids on thermal decomposition of tocopherol in various fatty acids and their methyl esters." Nippon Eiyo Shokuryo Gakkaishi 43, no. 2 (1990): 139–45. http://dx.doi.org/10.4327/jsnfs.43.139.

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27

Cheng, Hong-Jian, Ya-Li Shen, Shi-Yi Zhang, et al. "Three Coordination Polymers Constructed with Zinc(II), 3,3′-Thiodipropionic Acid, and Bipyridyl Ligands: Syntheses, Crystal Structures and Luminescent Properties." Zeitschrift für anorganische und allgemeine Chemie 641, no. 8-9 (2015): 1575–80. http://dx.doi.org/10.1002/zaac.201500167.

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28

KAJIMOTO, Goro, Hiromi YOSHIDA, and Akira SHIBAHARA. "Effects of lecithin, and of gallic and thiodipropionic acids on the thermal decomposition of tocopherols in heated hardened vegetable oils." Nippon Eiyo Shokuryo Gakkaishi 40, no. 4 (1987): 321–27. http://dx.doi.org/10.4327/jsnfs.40.321.

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29

Patil, Chandrashekhar K., Harishchandra D. Jirimali, Mahendra S. Mahajan, Jayasinh S. Paradeshi, Bhushan L. Chaudhari, and Vikas V. Gite. "Functional anti-corrosive and anti-bacterial surface coatings based on mercaptosuccinic and thiodipropionic acids and algae oil as renewable feedstock." Reactive and Functional Polymers 139 (June 2019): 142–52. http://dx.doi.org/10.1016/j.reactfunctpolym.2019.03.020.

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30

Pedireddi, V. R. "Design and Synthesis of Novel Aza-Aromatic Host−Guest Complexes: Crystal Structures of 1,7-Phenanthroline with Thiodipropionic and Thiodiglycolic Acids." Crystal Growth & Design 1, no. 5 (2001): 383–85. http://dx.doi.org/10.1021/cg015511r.

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31

Yang, Pei-Pei, Bing Li, Yu-Hu Wang, Wen Gu, and Xin Liu. "Synthesis, Structure, and Luminescence Properties of Zinc(II) and Cadmium(II) Complexes containing the Flexible Ligand of 3,3′-Thiodipropionic Acid." Zeitschrift für anorganische und allgemeine Chemie 634, no. 6-7 (2008): 1221–24. http://dx.doi.org/10.1002/zaac.200700597.

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32

Reddy, M. Venkateswar, and Alexander Steinbüchel. "3,3′-Thiodipropionic acid (TDP), a possible precursor for the synthesis of polythioesters: identification of TDP transport proteins in Variovorax paradoxus TBEA6." Applied Microbiology and Biotechnology 105, no. 9 (2021): 3733–43. http://dx.doi.org/10.1007/s00253-021-11294-y.

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Abstract3,3′-Thiodipropionic acid (TDP) is an antioxidant, which can be used as precursor carbon source to synthesize polythioesters. The bacterium Variovorax paradoxus TBEA6 strain can use TDP as a single source of carbon and energy. In the present study, experiments were carried out to identify proteins involved in the transport of TDP into the cells of strain TBEA6. Hence, eight putative tctC genes, which encode for the TctC proteins, were amplified from genomic DNA of TBEA6 strain using polymerase chain reaction and expressed in E. coli BL21 cells. Cells were grown in auto-induction medium
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33

Wenning, Leonie, Nadine Stöveken, Jan Hendrik Wübbeler, and Alexander Steinbüchel. "Substrate and Cofactor Range Differences of Two Cysteine Dioxygenases from Ralstonia eutropha H16." Applied and Environmental Microbiology 82, no. 3 (2015): 910–21. http://dx.doi.org/10.1128/aem.02568-15.

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ABSTRACTCysteine dioxygenases (Cdos), which catalyze the sulfoxidation of cysteine to cysteine sulfinic acid (CSA), have been extensively studied in eukaryotes because of their roles in several diseases. In contrast, only a few prokaryotic enzymes of this type have been investigated. InRalstonia eutrophaH16, two Cdo homologues (CdoA and CdoB) have been identified previously.In vivostudies showed thatEscherichia colicells expressing CdoA could convert 3-mercaptopropionate (3MP) to 3-sulfinopropionate (3SP), whereas no 3SP could be detected in cells expressing CdoB. The objective of this study w
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34

Dutta, Riya. "Editorial." Mapana Journal of Sciences 15, no. 2 (2016): v. http://dx.doi.org/10.12723/mjs.37.0.

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Mapana J Sci, 15, 2 (2016)ISSN 0975-3303|http://dx.doi.org/10.12723/mjs.37.0EditorialThis issue of Mapana—Journal of Sciences is devoted to research articles from Chemical Sciences. Researchers from various universities have contributed to the present issue. The first article is on ‘Studies on Ruthenium and Rhodium Complexes Containing 1,2- bis(N-Methylbenzimidazolyl) Benzene and Catalytic Transfer Hydrogenation’ by Hunasekatte G Bheemanna et al. The second article by Rita Bhattacharjee et al. is on ‘Synthesis and Characterization of Palladium(II) Complexes with Substituted Dihydrobenzoimidazo
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35

Bharathi, S., V. Yegnaraman, and G. Prabhakara Rao. "Molecular Recognition of Alkali Metal Cations by a Nickel Hexacyanoferrate Monolayer Anchored to Self-Assembled Monolayers of 3,3'-Thiodipropionic Acid on Gold." Langmuir 11, no. 2 (1995): 666–68. http://dx.doi.org/10.1021/la00002a052.

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36

Bruland, Nadine, Jan Hendrik Wübbeler, and Alexander Steinbüchel. "3-Mercaptopropionate Dioxygenase, a Cysteine Dioxygenase Homologue, Catalyzes the Initial Step of 3-Mercaptopropionate Catabolism in the 3,3-Thiodipropionic Acid-degrading BacteriumVariovorax paradoxus." Journal of Biological Chemistry 284, no. 1 (2008): 660–72. http://dx.doi.org/10.1074/jbc.m806762200.

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37

Wübbeler, Jan Hendrik, Sebastian Hiessl, Christina Meinert, et al. "The genome of Variovorax paradoxus strain TBEA6 provides new understandings for the catabolism of 3,3′-thiodipropionic acid and hence the production of polythioesters." Journal of Biotechnology 209 (September 2015): 85–95. http://dx.doi.org/10.1016/j.jbiotec.2015.06.390.

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38

Fehling, E., E. Klein, K. Vosmann, K. Bergander та N. Weber. "Linear copolymeric poly(thia-alkanedioates) by lipase-catalyzed esterification and transesterification of 3,3′-thiodipropionic acid and its dimethyl ester with α,ω-alkanediols". Biotechnology and Bioengineering 99, № 5 (2008): 1074–84. http://dx.doi.org/10.1002/bit.21704.

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39

Wübbeler, Jan Hendrik, Nadine Bruland, Milena Wozniczka, and Alexander Steinbüchel. "Biodegradation of the xenobiotic organic disulphide 4,4′-dithiodibutyric acid by Rhodococcus erythropolis strain MI2 and comparison with the microbial utilization of 3,3′-dithiodipropionic acid and 3,3′-thiodipropionic acid." Microbiology 156, no. 4 (2010): 1221–33. http://dx.doi.org/10.1099/mic.0.036178-0.

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Application of the non-toxic 3,3′-thiodipropionic acid (TDP) and 3,3′-dithiodipropionic acid (DTDP) as precursors for the microbial production of polythioesters (PTEs), a class of biologically persistent biopolymers containing sulphur in the backbone, was successfully established previously. However, synthesis of PTEs containing 4-mercaptobutyrate (4MB) as building blocks could not be achieved. The very harmful 4MB is not used as a PTE precursor or as the carbon source for growth by any known strain. As a promising alternative, the harmless oxidized disulfide of two molecules of 4MB, 4,4′-dith
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40

Kudelski, Andrzej, Agnieszka Michota, and Jolanta Bukowska. "Monolayers of sulfur-containing molecules at metal surfaces as studied using SERS: 3, 3′-thiodipropionic acid and 3-mercaptopropionic acid adsorbed on silver and copper." Journal of Raman Spectroscopy 36, no. 6-7 (2005): 709–14. http://dx.doi.org/10.1002/jrs.1342.

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41

Łuczak, Teresa. "Epinephrine Oxidation in the Presence of Interfering Molecules on Gold and Gold Electrodes modified with Gold Nanoparticles and Thiodipropionic Acid in Aqueous Solution. A Comparative Study." Electroanalysis 21, no. 23 (2009): 2557–62. http://dx.doi.org/10.1002/elan.200900303.

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42

"Amperometric Trace Determination of Rh(III) and Os(VIII) with Thiodipropionic Acid." ECS Meeting Abstracts, 2013. http://dx.doi.org/10.1149/ma2013-01/40/1413.

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43

Tella, Adedibu C., Samson O. Owalude, Vincent O. Adimula, et al. "Synthesis, Structure, and Properties of a Dinuclear Cu(II) Coordination Polymer Based on Quinoxaline and 3,3-Thiodipropionic Acid Ligands." Journal of Inorganic and Organometallic Polymers and Materials, March 24, 2021. http://dx.doi.org/10.1007/s10904-021-01966-7.

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44

KUMAR, A., and B. D. TILAK. "ChemInform Abstract: Esters of Thiodiglycollic and Thiodipropionic Acids and 2,5-Dicarboxy-3,4-dihydroxythiophene as Potential Slow Acting Anticancer Agents." ChemInform 18, no. 6 (1987). http://dx.doi.org/10.1002/chin.198706123.

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45

"Scientific Opinion on the safety evaluation of the substance, thiodipropionic acid, ditetradecyl ester, CAS No. 16545-54-3, for use in food contact materials." EFSA Journal 9, no. 4 (2011): 2126. http://dx.doi.org/10.2903/j.efsa.2011.2126.

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