3,4-Dichloroaniline structure
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Common Name | 3,4-Dichloroaniline | ||
|---|---|---|---|---|
| CAS Number | 95-76-1 | Molecular Weight | 162.017 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 271.8±20.0 °C at 760 mmHg | |
| Molecular Formula | C6H5Cl2N | Melting Point | 69-71 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 118.2±21.8 °C | |
| Symbol |
GHS05, GHS06, GHS09 |
Signal Word | Danger | |
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Microfunnel-supported liquid-phase microextraction: application to extraction and determination of Irgarol 1051 and diuron in the Persian Gulf seawater samples.
J. Chromatogr. A. 1356 , 32-7, (2014) In the present work, microfunnel-supported liquid-phase microextraction method (MF-LPME) based on applying low density organic solvent was developed for the determination of antifoulings (Irgarol 1051, diuron and 3,4-dichloroaniline) from seawater samples. In... |
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Effects of solvents and dosing procedure on chemical toxicity in cell-based in vitro assays.
Environ. Sci. Technol. 44(12) , 4775-81, (2010) Due to the implementation of new legislation, such as REACh, a dramatic increase of animal use for toxicity testing is expected and the search for alternatives is timely. Cell-based in vitro assays are promising alternatives. However, the behavior of chemical... |
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Population growth rate responses of Ceriodaphnia dubia to ternary mixtures of specific acting chemicals: pharmacological versus ecotoxicological modes of action.
Environ. Sci. Technol. 46(17) , 9663-72, (2012) When considering joint toxic apical effects at higher levels of biological organization, such as the growth of populations, the so-called pharmacological mode of action that relies on toxicological mechanistic effects on molecular target sites may not be rele... |
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Comparison of substrate specificity among human arylacetamide deacetylase and carboxylesterases.
Eur. J. Pharm. Sci. 78 , 47-53, (2015) Human arylacetamide deacetylase (AADAC) is an esterase responsible for the hydrolysis of some drugs, including flutamide, indiplon, phenacetin, and rifamycins. AADAC is highly expressed in the human liver, where carboxylesterase (CES) enzymes, namely, CES1 an... |
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Dissipation of triclosan, triclocarban, carbamazepine and naproxen in agricultural soil following surface or sub-surface application of dewatered municipal biosolids.
Sci. Total Environ. 512-513 , 480-8, (2015) In many jurisdictions land application of municipal biosolids is a valued source of nutrients for crop production. The practice must be managed to ensure that crops and adjacent water are not subject to contamination by pharmaceuticals or other organic contam... |
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[Determination of linuron and its metabolite 3,4-dichloroaniline residues in meat and meat products using liquid chromatography-tandem mass spectrometry].
Se Pu 29(10) , 967-73, (2011) A method of liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the determination of linuron and its metabolite 3, 4-dichloroaniline residues in pork, liver, kidney, casings, canned steam pork and sausage. The sample was extracted with... |
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HylA, an alternative hydrolase for initiation of catabolism of the phenylurea herbicide linuron in Variovorax sp. strains.
Appl. Environ. Microbiol. 79(17) , 5258-63, (2013) Variovorax sp. strain WDL1, which mineralizes the phenylurea herbicide linuron, expresses a novel linuron-hydrolyzing enzyme, HylA, that converts linuron to 3,4-dichloroaniline (DCA). The enzyme is distinct from the linuron hydrolase LibA enzyme recently iden... |
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The potential of individual based population models to extrapolate effects measured at standardized test conditions to relevant environmental conditions--an example for 3,4-dichloroaniline on Daphnia magna.
J. Environ. Monit. 12(11) , 2070-9, (2010) In current risk assessment ecotoxicological biotests (e.g.Daphnia reproduction test) are used to assess the potential impact of xenobiotics on ecosystems. The effects of chemicals and pesticides on populations of non-target organisms in the field depend not o... |
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Characterization of the propanil biodegradation pathway in Sphingomonas sp. Y57 and cloning of the propanil hydrolase gene prpH.
J. Hazard. Mater. 196 , 412-9, (2011) In our previous study, the isoproturon-degrading strain Sphingomonas sp. Y57 was isolated from the wastewater treatment system of an herbicide factory. Interestingly, this strain also showed the ability to degrade propanil (3,4-dichloropropionamilide). The pr... |
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Propionate addition enhances the biodegradation of the xenobiotic herbicide propanil and its metabolite.
Bioresour. Technol. 127 , 195-201, (2013) This study investigated ways of stimulating the biodegradation rates of the commonly applied herbicide, 3,4-dichloropropionanilide (propanil), and its metabolite, 3,4-dichloroaniline (DCA), as well as the growth rate of propanil- and DCA-degrading organisms i... |