![]() Pyromellitic acid structure
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Common Name | Pyromellitic acid | ||
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CAS Number | 89-05-4 | Molecular Weight | 254.150 | |
Density | 1.8±0.1 g/cm3 | Boiling Point | 585.8±50.0 °C at 760 mmHg | |
Molecular Formula | C10H6O8 | Melting Point | 281-284.5 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 322.1±26.6 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Short-column anion-exchange chromatography for soil and peat humic substances profiling by step-wise gradient of high pH aqueous sodium ethylenediaminetetraacetate.
J. Chromatogr. A. 1408 , 72-7, (2015) Novel anion-exchange liquid chromatographic method with step gradient of aqueous EDTA(4-) based mobile phase elution has been developed to profile available Slovak soil humic substances and alkaline extracts of various soils. The method utilize short glass co... |
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Benzenepolycarboxylic acids with potential anti-hemorrhagic properties and structure–activity relationships
Bioorg. Med. Chem. 19 , 7000-2, (2011) Previously, we reported the structural requirements of the cinnamic acid relatives for inhibition of snake venom hemorrhagic action. In the present study, we examined the effect of benzenepolycarboxylic acids and substituted benzoic acids against Protobothrop... |
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Effects of natural organic matter model compounds on the transformation of carbon tetrachloride by chloride green rust.
Water Res. 44(7) , 2125-32, (2010) Interest has grown in the use of reactive minerals for natural and engineered transformation of ground water contaminants. This study investigated how the structural properties of 10 model compounds representing natural organic matter (NOM) influenced their a... |
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New support for the affinity chromatography of hemoglobin.
J. Chromatogr. B. Biomed. Sci. Appl. 694(1) , 39-48, (1997) A new support for affinity chromatography of hemoglobin was synthesised from EAH Sepharose-4B containing a hexamethylamine spacer. Benzenetetracarboxylic (BTC) or benzenehexacarboxylic (BHC) acids were covalently bound to the spacer arm. At pH close to the pI... |
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Pyrones to pyrans: enantioselective radical additions to acyloxy pyrones.
J. Am. Chem. Soc. 128(41) , 13346-7, (2006) This paper describes a highly site-, diastereo-, and enantioselective intermolecular radical addition/hydrogen atom transfer to hydroxypyrone pyromeconic and kojic acids. The methodology can be extended to the formation of chiral quaternary centers. The produ... |
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Modification and validation of the pyromellitic acid electrolyte for the capillary electrophoretic determination of anions.
J. Chromatogr. A. 995(1-2) , 217-26, (2003) For the determination of inorganic and organic anions, the pyromellitic acid (PMA) electrolyte is widely used. The pH adjustment of the self-prepared electrolyte was very challenging to satisfy the pH of specification of pH 7.8 +/- 0.1. A modification was pro... |
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Ion-exclusion chromatography of carboxylic acids on silica gel modified with aluminium.
J. Chromatogr. A. 850(1-2) , 177-85, (1999) The modification of silica gel with aluminium by a coating method was effective for the preparation of a silica-based stationary phase, which acted as a cation exchanger under strongly acidic conditions. In order to expand the utility of the laboratory-made a... |
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Purification and characterization of fumarase from Corynebacterium glutamicum.
Biosci. Biotechnol. Biochem. 70(5) , 1102-9, (2006) Fumarase (EC 4.2.1.2) from Corynebacterium glutamicum (Brevibacterium flavum) ATCC 14067 was purified to homogeneity. Its amino-terminal sequence (residues 1 to 30) corresponded to the sequence (residues 6 to 35) of the deduced product of the fumarase gene of... |
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Application of zirconium-modified silica gel as a stationary phase in the ion-exclusion chromatography of carboxylic acids. II. Separation of aliphatic carboxylic acids with pyromellitic acid as eluent and with suppressed conductimetric detection.
J. Chromatogr. A. 920(1-2) , 181-91, (2001) The application of zirconium-modified silica gels (Zr-Silica) as stationary phases for ion-exclusion chromatography with conductimetric detection (IEC-CD) for C1-C8 aliphatic carboxylic acids (formic, acetic, propionic, butyric, valeric, caproic, heptanoic an... |
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Relationship between chromatographic properties of aromatic carboxylic acids and their structure.
J. Chromatogr. A. 948(1-2) , 65-7, (2002) The retention of aromatic carboxylic acids and their esters in reversed-phase HPLC is proportional to the sum of their partition coefficients in octanol-water system and retention increments. This equation can be used for the identification of various side-pr... |