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10 Gram |
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99% Maduramycin Ammonium Maduramycin Ammonium Manufacturer Anticoccidial Drugs
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Maduramycin ammonium Basic information |
Product Name: | Maduramycin ammonium |
Synonyms: | Maduramincin ammonium;Maduramicin ammonium premix;MADURAMICIN AMMONIUM 90%;2H-Pyran-2-acetic acid, 6-(1R)-1-(2S,5R,7S,8R,9S)-2-(2S,2R,3S,5R,5R)-3-(2,6-dideoxy-3,4-di-O-methyl-.beta.-L-arabino-hexopyranosyl)oxyoctahydro-2-methyl-5-(2S,3S,5R,6S)-tetrahydro-6-hydroxy-3,5,6-trimethyl-2H-pyran-2-yl2,2-bifuran-5-yl-9-hydroxy-2,8-dimet;Maduraminic Ammonium;Cygro;Maduramicin;Prinicin ammonium |
CAS: | 84878-61-5 |
MF: | C47H83NO17 |
MW: | 934.16 |
EINECS: | 200-771-5 |
Product Categories: | Active Pharmaceutical Ingredients;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;API's |
Mol File: | 84878-61-5.mol |
Maduramycin ammonium Chemical Properties |
Melting point | 173-176 °C |
storage temp. | 0-6°C |
Safety Information |
Hazard Codes | T+ |
Risk Statements | 25-27-36 |
Safety Statements | 26-28-36/37-45 |
RIDADR | UN 2811 |
HazardClass | 6.1 |
PackingGroup | III |
Maduramycin ammonium Usage And Synthesis |
Chemical Properties | White Solid |
Uses | Maduramcin ammonium is prepared from maduramicin by taking advantage of the acidic carboxylic acid which ionises and readily forms the salt in ammonium hydroxide solutions. The ammonium salt is the preferred formulation in animals to prevent coccidiosis and to promote growth. Maduramicin is also active against Treponema and Cryptosporidium. Maduramicin is an ionophore, forming complexes with monovalent cations, with a higher affinity for K+ than Na+. |
Uses | Maduramicin ammonium is prepared from maduramicin by taking advantage of the acidic carboxylic acid which ionises and readily forms the salt in ammonium hydroxide solutions. The ammonium salt is the preferred formulation in animals to prevent coccidiosis and to promote growth. Maduramicin is also active against Treponema and Cryptosporidium. Maduramicin is an ionophore, forming complexes with monovalent cations, with a higher affinity for K+ than Na+. |
Uses | Polyether antibiotic chemically related to the lonomycins. Coccidiostat |
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