Carbadox
 | |
| Names | |
|---|---|
| IUPAC names
methyl (2E)-2-[(1,4-dioxidoquinoxalin-2-yl) methylene]hydrazinecarboxylate | |
| Identifiers | |
6804-07-5  | |
| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL13779  |
| ChemSpider | 10606106 |
| ECHA InfoCard | 100.027.163 |
| EC Number | 229-879-0 |
| PubChem | 5353472 |
| RTECS number | FE2779000 |
| UNII | M2X04R2E2Y |
| |
| |
| Properties | |
| C11H10N4O4 | |
| Molar mass | 262.22 g/mol |
| Appearance | Yellow crystals |
| Density | 1.44 g/cm3 |
| Melting point | 239.5 °C |
| Insoluble | |
| Hazards | |
| EU classification (DSD) |
F, T |
| R/S statement | R: R45, R11, R22 S: S53, S45 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Carbadox is a veterinary drug that combats bacterial infection in swine, particularly swine dysentery. In early 2004, it was banned by the Canadian government as a livestock feed additive and for human consumption, since it is carcinogenic and induces birth defects, as was shown in animal experiments.[1] The European Union also forbids the use of carbadox at any level.[2] It is approved in the United States for use in swine for up to 42 days before slaughter,[3] but in 2016, the United States Food and Drug Administration moved to ban its use in pork, citing a potential cancer risk to humans.[4] Australia forbids the use of carbadox in food producing animals.[5]
References
- ↑ Maximum Residue Limits, Health Canada, retrieved 2010-07-27
- ↑ Ungemach, Fritz R. "WHO Food Additives Series: 51 CARBADOX (addendum)". WHO Food Additives Series. INCHEM. Retrieved 23 Mar 2015.
- ↑ "21CFR 558.115". Code of Federal Regulations. FDA. 1 Apr 2014. Retrieved 23 Mar 2015.
- ↑ Fox, Maggie. "FDA Moves to Ban Cancer-Causing Pork Antibiotic". NBC News. Retrieved 9 Apr 2016.
- ↑ Substances Not Permitted for use on Food-Producing Animals in Australia, Australian Pesticides and Veterinary Medicines Authority, retrieved 2010-08-31
This article is issued from Wikipedia - version of the 6/7/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.