3,4,5,6-Tetrahydrophthalic acid anhydride
3,4,5,6-Tetrahydrophthalic acid anhydride structure
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Common Name | 3,4,5,6-Tetrahydrophthalic acid anhydride | ||
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| CAS Number | 2426-02-0 | Molecular Weight | 152.147 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 302.3±11.0 °C at 760 mmHg | |
| Molecular Formula | C8H8O3 | Melting Point | 69-73 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 146.1±16.5 °C | |
| Symbol |
GHS05, GHS08 |
Signal Word | Danger | |
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[Data providing a basis for the MPEL of tetrahydrophthalic anhydride, tetrahydrophthalamide and hydroxymethyltetrahydrophthalimide in the air of the work environment].
Gig. Tr. Prof. Zabol. (12) , 37-8, (1985)
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Internal structure of ovomacroglobulin studied by electron microscopy.
J. Biol. Chem. 265(14) , 8280-4, (1990) As a model for the molecular structure of proteins belonging to the alpha 2-macroglobulin family, ovomacroglobulin of reptilian origin was studied by electron microscopy in the original tetrameric form as well as in the dissociated forms into half- and quarte... |
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Selective proteolytic digestion as a method for the modification of human HDL3 structure.
J. Lipid Res. 24(3) , 245-52, (1983) Trypsin digestion of human high density lipoprotein (d 1.125-1.21 g/ml) on which the lysine residues have been masked with the reversible blocking group, 2,3,4,5-tetrahydrophthallic anhydride (THPA), was found to result in the fragmentation of the apoA-I comp... |
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Amidization of doxorubicin alleviates doxorubicin-induced contractile dysfunction and reduced survival in murine cardiomyocytes.
Toxicol. Lett. 178(3) , 197-201, (2008) Doxorubicin is an effective anthracycline used for cancer therapy. However, the clinical application of doxorubicin has been largely limited by its irreversible cardiotoxicity, which is mainly induced by the primary amine group. In this study, we structurally... |
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3,4,5,6-Tetrahydrophthalic anhydride modification of glutamate dehydrogenase: the construction and activity of heterohexamers.
Arch. Biochem. Biophys. 263(2) , 315-22, (1988) Modification of glutamate dehydrogenase with 3,4,5,6-tetrahydrophthalic anhydride at pH 8.0 results in the progressive loss of enzymatic activity and a concomitant increase in the negative charge of the protein. Although the rate of inactivation at room tempe... |