China CAS 51004-33-2 Avilamycin for Veterinary, Find details about China Avilamycin, Avilamycin Powder from CAS 51004-33-2 Avilamycin for Veterinary
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Product Name | Avilamycin |
Appearance | white Powder |
Assay | 98% min levamisole |
Test | HPLC |
Certificate | ISO 9001 |
CAS | 11051-71-1 |
MF | C11H12N2S |
Storage Temperature | Cool Dry Place |
Avilamycin is a new type of growth, promote the product can be used as pig and poultry feed additive, daily gain average raise pigs and chickens and the feed rate of return. Because of its without any treatment and prevention, so completely avoided by application of therapeutic antibiotics resistance.
Avilamycin is mainly effective against Gram-positive bacteria and poorly against Gram-negative bacteria. Among them, Avilamycin A has the highest activity, especially for Clostridium, Streptococcus and Bacillus; and Avilamycin B has the highest activity against Staphylococcus. Dosage: For piglets within 4 months of age, 20-40g per ton of feed; 6-month-old pigs plus 10-20g per ton of feed.
1. to mainten livestock and poultry intestinal flora balance
Indirect play to maintain intestinal wall integrity, assist use nutrient, synthetic part the body required vitamins, competitive inhibition pathogenic microorganism, decomposition antinutritional factors, stimulate immunity, such as action.
2. efficient kill or personal resource questionnaire part ii clostridium
Avila amphotericin to personal resource questionnaire part ii clostridium role powerful, long-term add avila amphotericin can lead to prevent personal resource questionnaire part ii clostridium disease role; To have taken place personal resource questionnaire part ii clostridium disease in livestock and poultry application can have auxiliary therapeutic action.
3. Can significantly improve livestock and poultry to lysine and methionine, cystine utilization; Adjust feed nutrient unbalance caused a sticky; Various improve feed utilization rate of the whole, the growth promoting excellent effect.
4. And a variety of resistance to ball insect drug compatibility application can enhance ball insect resistance effect.
Items | Specifications | Results | |
Appearance | White to off-white powder, | White powder, | |
Identification | Infared Absorption | Complies | |
The retention time of the major peak in the chromatogram of the Assay prepration corresponds to that in the chromatogram of the standard preparation, as obtained in the assay | complies | ||
Specific rotation | Between -28.6°and -35.0°, measured at 20° | -32.8° | |
Water | not more than 0.5% | 0.12% | |
residue on ignition | not more than 0.2% | 0.11% | |
Heavy metals | not more than 0.001% | complies | |
related compounds by HPLC(Test1) | Fructose not more than 0.3% Compound A not more than 0.3% Other individual impurity not more than 0.1% Total impurities not more than 0.5% | Fructose: 0.03% Compound A: 0.04% Total impurities: 0.07% | |
Particle size | 90% less than 350 microns | complies | |
Limit of sulfamate and sulfate | Sulfamate ion not more than 0.10% Sulfate ion not more than 0.10% | complies | |
Residual Solvent | Methylene Chloride not more than 250μg/g | not detected | |
Acetone not mor than 2500μg/g | |||
Isopropanol not more than 5000μg/g | |||
Ethanenitrile not more than 400μg/g | |||
n-hexane not more than 290μg/g | |||
Ethyl Acetate not more than 2500μg/g | |||
Pyridine not more than 100μg/g | |||
Assay | Topiramate contains not less than 98.0% and not more than the equivalent of 102.0% of C12H21NO8S, calculated with reference to the Anhydrous Basis | 99.80% | |
Conclustion | The material complies with respect to USP32 |