Tiletamine Hydrochloride CAS 14176-50-2
Product Details:
|
Nom du produit |
Tiletamine Hydrochloride |
|
Alias |
Tiletamine Hydrochloride;Cyclohexanone, 2-(ethylamino)-2-(2-thienyl)-,chlorhydrate;TiletamineI Hydrochloride;CI-634;CL-399;CN-54521-2; Nsc167740; Tiletamin hydrochloride |
|
CAS |
14176-50-2 |
|
MF |
C12H17NOS.ClH |
|
MW |
259.799 |
|
EINECS |
1312995-182-4 |
|
Pureté |
99% |
|
Apparence |
White to off-white Powder |
|
Attestation |
ISO 9001, USP, BP |
|
Standard |
Norme d'entreprise |
|
Classe |
Pharma Grade |
|
Usage |
Tiletamine is a receptor antagonist, an anesthetic. |
|
Espace de rangement |
Store in cool and dry area and keep away from direct sunlight |
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, hypotension, 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.
Dosage
If used alone the dose for sedation is 0.5 à 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
|
Nom du produit |
Tiletamine hydrochloride |
|
n ° CAS. |
14176-50-2 |
Emballage extérieur |
1kg/bag |
|
Date de production |
20170525 |
Durée de conservation |
20190524 |
|
Norme adoptée |
EP7.0 |
|
Éléments d'analyse |
spécification |
Résultats |
| Personnage |
Off-white to White Crystalline powder |
Off-White Crystalline powder |
| Solubilité |
soluble in Ethanol (96%), Almost insoluble in Dichloromethane |
Conforme |
| Identification |
Specific Rotation -67-69.5° (on anhydrate basis) |
-67.4 |
| Identification |
(2)ET:Meets the requirement. |
Conforme |
| Identification |
(3)Optical purity Test |
Conforme |
| Identification |
(4) Chloride Reaction |
Conforme |
| Clarity |
Clear,not deeper than Y6. |
Conforme |
| PH |
2.8-3.4 |
2.9 |
| Substances apparentées |
Impurity A≤0.15% |
0.03% |
| Substances apparentées |
Impurity B≤0.15% |
Not detected |
| Substances apparentées |
Impurity C ≤0.15% |
0.04% |
| Substances apparentées |
Unknown single impurity ≤0.15% |
0.07% |
| Substances apparentées |
0.1% Total Impurity≤0.5% |
0.18% |
| Impurity D |
Impurity D≤0. 5% |
0.05% |
| L'eau |
4.5%-6.5% |
5.7% |
| Métaux lourds |
10 ppm |
se conforme |
| Sulfate Ash |
≤0.1% |
0.04% |
| Essai |
99.0%~101.0% |
99.4% |
|
Conclusion |
Qualifié |
Directeur commercial