4-Chloro-3,5-dinitrobenzoic acid
4-Chloro-3,5-dinitrobenzoic acid structure
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Common Name | 4-Chloro-3,5-dinitrobenzoic acid | ||
|---|---|---|---|---|
| CAS Number | 118-97-8 | Molecular Weight | 246.561 | |
| Density | 1.8±0.1 g/cm3 | Boiling Point | 422.7±45.0 °C at 760 mmHg | |
| Molecular Formula | C7H3ClN2O6 | Melting Point | 159-162 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 209.4±28.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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The modulation of cytochrome c electron self-exchange by site-specific chemical modification and anion binding.
FEBS Lett. 206(1) , 15-9, (1986) The site-specific chemical modification of horse heart cytochrome c at Lys-13 and -72 using 4-chloro-3,5-dinitrobenzoic acid (CDNB) increases the electron self-exchange rate of the protein. In the presence of 0.24 M cacodylate (pH* 7.0) the electron self-exch... |
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Localization of lysine residues in the binding domain of the K99 fibrillar subunit of enterotoxigenic Escherichia coli.
Biochim. Biophys. Acta 872(1-2) , 92-7, (1986) Modification of lysine residues with 4-chloro-3,5-dinitrobenzoate results in the loss of the binding capacity of K99 fibrillae to horse erythrocytes (Jacobs, A.A.C., van Mechelen, J.R. and de Graaf, F.K. (1985) Biochim. Biophys. Acta 832, 148-155). In the pre... |
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Threshold levels in toxicology: significance of inactivation mechanisms.
Adv. Exp. Med. Biol. 136 Pt B , 1389-98, (1981) Metabolic inactivation of chemicals may prevent toxic effects of reactive intermediates when present at low levels whereas inactivation may be overcome at high levels changing dose-effect relation. This is demonstrated in various in vitro test systems: a) Mon... |
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Chemical modification of spinach plastocyanin using 4-chloro-3,5-dinitrobenzoic acid: characterization of four singly-modified forms.
Biochim. Biophys. Acta 1016(1) , 107-14, (1990) Chemical modification of plastocyanin was carried out using 4-chloro-3,5-dinitrobenzoic acid, which has the effect of replacing positive charges on amino groups with negatively charged carboxyl groups. Four singly-modified forms were obtained which were separ... |
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Chemical modification of amino groups in cardiotoxin III from Taiwan cobra Naja naja atra) venom.
Biochem. Mol. Biol. Int. 31(1) , 175-84, (1993) Cardiotoxin III (CTX III), a major cardiotoxin analogue isolated from the Taiwan cobra (Naja naja atra) venom was modified, either with trinitrobenzene sulfonate (TNBS) or 4-chloro-3,5-dinitrobenzoate (CDNB). Under the conditions of limited reagent availabili... |
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Enzymatic dehalogenation of chlorinated nitroaromatic compounds.
Appl. Environ. Microbiol. 54(5) , 1199-202, (1988) 4-Chlorobenzoate dehalogenase from Pseudomonas sp. strain CBS3 converted 4-chloro-3,5-dinitrobenzoate to 3,5-dinitro-4-hydroxybenzoate and 1-chloro-2,4-dinitrobenzene to 2,4-dinitrophenol. The activities were 0.13 mU/mg of protein for 4-chloro-3,5-dinitrobenz... |
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Chemical modification of Lys-6 in Taiwan cobra phospholipase A2 with 4-chloro-3,5-dinitrobenzoate.
Biochem. Mol. Biol. Int. 33(6) , 1207-13, (1994) Phospholipase A2 (PLA2) from Naja naja atra snake venom was modified with 4-chloro-3,5-dinitrobenzoate, and one major carboxydinitrophenylated (CDNP) PLA2 was separated by high performance liquid chromato-graphy. CDNP-PLA2 contained only one CDNP group on Lys... |
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Physicochemical and toxicological studies on 4-chloro-3,5-dinitrobenzoic acid in aqueous solutions.
Environ. Toxicol. Chem. 23(5) , 1129-35, (2004) Physicochemical characterization of hazardous compounds often is required for the development of structure-reactivity correlations. Physical, chemical, and toxicological properties of target pollutants require determination for an efficient application of was... |