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Isophthalic Acid (isophthalic + acid)
Selected AbstractsChemInform Abstract: Synthesis and Antimicrobial Properties of the Products of Monothiocyanatoarylation of Diallyl Esters of Phthalic and Isophthalic Acids.CHEMINFORM, Issue 32 2002P. M. Gorbovoi Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Hydrophobic derivatives of 5-(hydroxymethyl)isophthalic acid that selectively induce apoptosis in leukemia cells but not in fibroblasts,,DRUG DEVELOPMENT RESEARCH, Issue 4 2008Anna Galkin Abstract New apoptosis modulating agents are widely sought, because failure in regulation of apoptosis is associated with many diseases. In this study, we have evaluated apoptosis inducing the potential of ten new hydrophobic derivatives of 5-(hydroxymethyl)isophthalic acid. Cancerous leukemia cells (HL-60) and non-malignant fibroblasts (Swiss 3T3) were incubated with test compounds for 24,h and morphologically evaluated. The changes in mitochondrial membrane potential (,,m) and caspase-3 activity were used to confirm the results and to study early induction of apoptosis. Cytotoxicity was determined using the lactate dehydrogenase (LDH) assay and mutagenicity with miniaturized Ames-test. The most potent selective apoptosis inducers were compounds 1c and 1,h having IC50 values of 41 and 23,µM, respectively, in leukemia cells (HL-60) while effects in fibroblasts (Swiss 3T3) were insignificant. Reduction of ,,m and increase in caspase-3 activity were observed already during the first 2,hr in the HL-60 cells treated with compounds 1,c and 1,h. Neither of the compounds was cytotoxic or mutagenic. The results indicate that compounds 1,c and 1,h are selective apoptosis inducers and should be studied further for possible use in cancer therapy. Drug Dev. Res. 69: 185,195, 2008. © 2008 Wiley-Liss, Inc. [source] A C2 -Chiral Bis(amidinium) Catalyst for a Diels,Alder Reaction Constituting the Key Step of the Quinkert,Dane Estrone SynthesisEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 9 2003Svetlana B. Tsogoeva Abstract A novel C2 -chiral bis(amidinium) salt 12 has been synthesised from 5-(tert -butyl)isophthalic acid. The hydrogen-bond-mediated association of dienophiles 3a and 3b with the chiral host molecule 12 accelerates the Diels,Alder reactions with diene 2 by more than three orders of magnitude. In addition, enantioselective formation of the desired adducts is observed under catalysis with 12. Good ratios of 4a(b) + ent - 4a(b)/5a(b) + ent - 5a(b) from 1:10 to 1:22 were found in all reactions. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source] Poly(ethylene terephthalate) recycling and recovery of pure terephthalic acid by alkaline hydrolysisADVANCES IN POLYMER TECHNOLOGY, Issue 4 2002G. P. Karayannidis Abstract Poly(ethylene terephthalate) (PET) taken from postconsumer soft-drink bottles was subjected to alkaline hydrolysis after cutting it into small pieces (flakes). The reaction took place in an autoclave at 120,200°C with aqueous NaOH solutions and at 110,120°C with a nonaqueous solution of KOH in methyl Cellosolve. The disodium or dipotassium terephthalate received was treated with sulfuric acid and terephthalic acid (TPA) of high purity was separated. The 1H NMR spectrum of the TPA revealed an about 2% admixture of isophthalic acid together with the pure 98% TPA. The purity of the TPA obtained was tested by determining its acidity and by polymerizing it with ethylene glycol by using tetrabutyl titanate as catalyst. A simple theoretical model was developed to describe the hydrolysis rate. The activation energy calculated was 99 kJ/mol. This method is very useful in recycling of PET bottles and other containers because nowadays TPA is replacing dimethyl terephthalate (the traditional monomer) as the main monomer in the industrial production of PET. © 2002 Wiley Periodicals, Inc. Adv Polym Techn 21: 250,259, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.10029 [source] Dehydration of benzene through fluorine containing aromatic polyamide membrane by pervaporationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008P. K. Gutch Abstract A series of soluble polyamides were synthesized by direct polycondensation of the 5- tert -butyl isophthalic acid with different diamines. Solution (20%) of the polymers in suitable solvents was used to cast the membranes. The membranes showed selectivity toward the benzene (Bz) in a mixture of Bz/water (H2O). Water affinity of the membrane was found to be lower than that of Bz. The polyamide incorporating hexafluoro isopropylidene moiety was promising for the dehydaration of Bz and breaking of Bz/H2O azeotrope. The polymers exhibited inherent viscosities, ranging from 0.40 to 0.92 dL/g and 10% weight loss in synthetic air up to 474°C. Glass transition temperature measured by DSC and DMA reached up to 258°C. The membranes were pale yellow in appearance having tensile strength up to 85 MPa, modulus of elasticity up to 2.6 GPa, and elongation at break up to 9.5%, depending upon the exact repeating unit structure. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Safety of Polyethylene Terephthalate Food Containers Evaluated by HPLC, Migration Test, and Estimated Daily IntakeJOURNAL OF FOOD SCIENCE, Issue 6 2008H.-J. Park ABSTRACT:, A comparative high-pressure liquid chromatography (HPLC) analysis of monomers, terephthalic acid (TPA), isophthalic acid (IPA), and dimethyl terephthalate (DMT) from polyethylene terephthalate (PET) food containers was conducted. Monomer linearities and sensitivities were calibrated between established and novel HPLC analyses. Safety of PET containers was evaluated with newly established detection methods for TPA, IPA, and DMT. Migration of the 3 monomers into food simulants (water, 4% acetic acid, 20% alcohol, and n-heptane) from 56 PET containers collected from open markets was monitored. Migrated monomers were not detected over 0.1 ppm of detection limit. The corresponding estimated daily intake was measured to confirm the safety of these publicly available PET containers and to permit comparison to the specific migration limit of the European Union. The estimated daily intake of 3 monomers migrating from PET was 0.0384 mg/kg each. This represented only 0.6% of the European Union's specific migration limit, confirming the safety of the examined containers. [source] Development of amorphous copolyesters based on 1,4-cyclohexanedimethanolJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 23 2004S. Richard Turner Abstract The modification of poly(ethylene terephthalate) with 1,4-cyclohexanedimethanol and the modification of poly(1,4-cyclohexylenedimethylene terephthalate) with ethylene glycol or isophthalic acid retard the crystallization of the copolyester backbone, and over a wide range of comonomer concentrations, very slowly crystallizing, essentially amorphous copolyesters are formed. These amorphous copolyesters possess attractive physical properties such as toughness, low color, and chemical resistance, and since their first commercial introduction in 1977, these copolyesters have become the basis of a large and growing plastics business for Eastman Chemical Co. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5847,5852, 2004 [source] Modification of polycondensation of isophthalic and terephthalic acids and bisphenols with tosyl chloride/dimethylformamide/pyridine by the presence of additivesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 7 2003Fukuji Higashi Abstract In copolycondensation with 2,2-bis(4-hydroxyphenyl)propane (BPP) and bisphenols (BPs) containing various alkylidene linkages, the associative interactions between BP moieties in the resulting oligomers most likely affected the reaction. To modify the interactions to favorably control the reaction, several additives were examined in a two-stage polycondensation of an equimolar mixture of isophthalic acid and terephthalic acid, first with BPP (50 mol %) and next with additional BPP. Of additives used, diphenylmethane of an equivalent to BPP in the preformed oligomers was most effective. The results are discussed in terms of the distributions of resulting oligomers prepared at 70% extent of reaction. Better results were obtained when the distributions showed profiles similar to the theoretical one calculated on the basis that the reactivity of the oligomers is the same independent of their chain lengths. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 970,975, 2003 [source] | |||||||||||||