As a result, a series of new high-molecular-weight 1,2,3-triazole ring-containing aliphatic "click" PEs on the basis of nontoxic building blocks, fatty diols and dicarboxylic acids
, were obtained.
Shi, "Synthesis, characterization and fluorescence properties of novel pyridine dicarboxylic acid
derivatives and corresponding Tb(III) complexes," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol.
LC-MS GC-MS Retention Chemical names Retention Chemical names time/min time/min 4.5 2,6-Naphthalene 2.67 Ethylene glycol dicarboxylic acid
3.9 Phthalic acid 4.39 Diethylene glycol
5-hydroxymethyl-2furancarboxylic acid (HFCA), 5-formyl-2-furan carboxylic acid (FFCA), 2,5-Furan dicarboxylic acid
(FDCA) and 2,5-dihydroxymethylfurfural (DHMF).
Reinhard, "Electrochemical characterisation of the ability of dicarboxylic acid
salts to the corrosion inhibition of mild steel in aqueous solutions," Corrosion Science, vol.
Azelaic Acid (20%): It is a naturally occurring dicarboxylic acid
which acts by anti- tyrosinase activity.
In fact, for the most recent NHANES survey (2011-2012), scientists at the Centers for Disease Control and Prevention are beginning to release population-level data for the urinary metabolite of 1,2-cyclohexane dicarboxylic acid
diisononyl ester (DINCH), a nonphthalate plasticizer that is used as a replacement for some of the high-molecular-weight phthalates (Centers for Disease Control and Prevention 2013).
Elatur CH is a 1,2-cyclohexane dicarboxylic acid
In this account, 9,17-octadecadienal (Z)-, an unsaturated aldehyde (peak area: 21.77%) (Figure 4(e)), n-hexadecanoic acid, a palmitic acid (peak area: 21.75%) (Figure 4(f)), phthalic acid, di(2-propylpentyl) ester, a dicarboxylic acid
ester (peak area: 9.48%), and 9,12-octadecadienoic acid (Z,Z)-, a linolenic acid (peak area: 9.35%) were the major phytochemicals on the basis of quantity.
3,3-Diaminobenzidine and pyridine-2,5- dicarboxylic acid
were subjected for reaction in a flask and then polyphosphoric acid in the presence of nitrogen atmosphere was added and heated up to 220[degrees]C for 30 hours.
This study revealed that a tricarboxylic acid (citric acid) is a stronger extraction agent than oxalic acid (a dicarboxylic acid
He proposed that 2-propylmyristic acid is oxidized from [omega]-methyl terminal by [omega]-oxidation because the substitution at the 2([alpha])-carbon atom hinders the usual [beta]-oxidation: the resulting dicarboxylic acid
is [beta]-oxidized (unilateral oxidation) from the unsubstituted end 4 times leaving the substituted adipic acid.