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| | 2,3,4,5-TETRACHLOROANILINE Basic information |
| Product Name: | 2,3,4,5-TETRACHLOROANILINE | | Synonyms: | GENTAMICIN SULFATE USP,EP;2,3,4,5-tetrachloroaniline solution;2,3,4,5-TETRACHLORANILLINE;Aniline, 2,3,4,5-tetrachloro-;2,3,4,5-TETRACHLOROANILINE;2,3,4,5-Tetrachloroaniline Solution, 100ppm;Benzenamine, 2,3,4,5-tetrachloro-;2,3,4,5-Tetrachloroaniline Solution in Acetonitrile, 100μg/mL | | CAS: | 634-83-3 | | MF: | C6H3Cl4N | | MW: | 230.91 | | EINECS: | 211-216-1 | | Product Categories: | Alphabetic;TA - TE | | Mol File: | 634-83-3.mol |  |
| | 2,3,4,5-TETRACHLOROANILINE Chemical Properties |
| Melting point | 118 °C | | Boiling point | 325.5±37.0 °C(Predicted) | | density | 1.655±0.06 g/cm3(Predicted) | | Fp | >100 °C | | storage temp. | 2-8°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | pka | -0.10±0.10(Predicted) | | color | Off-White to Pale Beige |
| | 2,3,4,5-TETRACHLOROANILINE Usage And Synthesis |
| Uses | 2,3,4,5-Tetrachloroaniline, is the metabolite of pentachloronitrobenzene (P237990), having fungicidal activities. It is also used as an intermediate for the synthesis of chlorinated compounds, such as polychlorinated biphenyls (PCBs). | | Purification Methods | Crystallise it from EtOH. The acetyl derivative has m 165-166o (from EtOH). [Beilstein 12 H 630, 12 I 313, 12 II 340, 12 IV 1286.] |
| | 2,3,4,5-TETRACHLOROANILINE Preparation Products And Raw materials |
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