Tiletamine Hydrochloride CAS 14176-50-2
Product Details:
|
nombre del producto |
Tiletamine Hydrochloride |
|
As |
Tiletamine Hydrochloride;Cyclohexanone, 2-(ethylamino)-2-(2-thienyl)-,clorhidrato;TiletamineI Hydrochloride;CI-634;CL-399;CN-54521-2; Nsc167740; Tiletamin hydrochloride |
|
CASO |
14176-50-2 |
|
MF |
C12H17NOS.ClH |
|
MW |
259.799 |
|
EINECS |
1312995-182-4 |
|
Pureza |
99% |
|
Apariencia |
White to off-white Powder |
|
Certificación |
YO ASI 9001, USP, PA |
|
Estándar |
Estándar empresarial |
|
Calificación |
Pharma Grade |
|
Uso |
Tiletamine is a receptor antagonist, an anesthetic. |
|
Almacenamiento |
Almacenar en un lugar fresco y seco y mantener alejado de la luz solar directa. |
Notice:
Do not use Tiletamine hydrochloride in dogs and cats with pancreatic disease, renal pathology or impairment of renal function, or severe cardiac or pulmonary dysfunction. Do not use for Caesarean section. Do not use phenothiazine-derivative drugs concomitantly with Tiletamine hydrochloride as the combination produces respiratory and myocardial depression, g/kg en ratas, and hypothermia. Pulmonary edema has been reported in cats. Respiratory depression may occur following administration of high doses of Tiletamine hydrochloride. For more safety information, please refer to the full Prescribing Information.
Dosis
If used alone the dose for sedation is 0.5 a 2.0 mg/kg body weight depending on the species and desired level of effect.
Uses and dose rates in combination with other drugs are found in.
Recommended route of administration is deep intramuscular injection.
Tiletamine hydrochloride COA
|
Nombre del producto |
Tiletamine hydrochloride |
|
CAS No. |
14176-50-2 |
Embalaje exterior |
1kg/bag |
|
Fecha de producción |
20170525 |
Duración |
20190524 |
|
Norma adoptada |
EP7.0 |
|
Elementos de análisis |
Especificación |
Resultados |
| Personaje |
Off-white to White Crystalline powder |
Off-White Crystalline powder |
| Solubilidad |
soluble in Ethanol (96%), Almost insoluble in Dichloromethane |
Cumple |
| Identificación |
Specific Rotation -67-69.5° (on anhydrate basis) |
-67.4 |
| Identificación |
(2)Y:Meets the requirement. |
Cumple |
| Identificación |
(3)Optical purity Test |
Cumple |
| Identificación |
(4) Chloride Reaction |
Cumple |
| Clarity |
Claro,not deeper than Y6. |
Cumple |
| PH |
2.8-3.4 |
2.9 |
| Sustancias relacionadas |
Impurity A≤0.15% |
0.03% |
| Sustancias relacionadas |
Impurity B≤0.15% |
No detectado |
| Sustancias relacionadas |
Impurity C ≤0.15% |
0.04% |
| Sustancias relacionadas |
Unknown single impurity ≤0.15% |
0.07% |
| Sustancias relacionadas |
0.1% Total Impurity≤0.5% |
0.18% |
| Impurity D |
Impurity D≤0. 5% |
0.05% |
| Agua |
4.5%-6.5% |
5.7% |
| Metales pesados |
≤10 ppm |
complies |
| Sulfate Ash |
≤0.1% |
0.04% |
| Ensayo |
99.0%~101.0% |
99.4% |
|
Conclusión |
Calificado |
Gerente de ventas