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Product Name: | Tiletamine Hydrochloride | Cas: | 14176-50-2 |
---|---|---|---|
Purity: | 99% | Appearance: | White Powder |
Usage: | Anesthesia Sedative | Grade: | Pharmaceutical Grade |
High Light: | pro anabolic steroids,procaine hcl powder |
Cyclohexanone Tetracaine HCL Powder For Anesthesia Sedative CAS 14176 50 2
Product Name: Tiletamine Hydrochloride
Synonyms:Cyclohexanone, 2-(ethylamino)-2-(2-thienyl)-, hydrochloride;Tiletamine Hydrochloride;Tiletamin hydrochloride
CAS:14176-50-2
MF: C12H17NOS.ClH
MW:259.799
Chemical Properties:White to off-white solid
Usage:Tiletamine is a receptor antagonist, an anesthetic.
Description:
Tiletamine hydrochloride is a dissociative anesthetic and pharmacologically classified as an NMDA receptor antagonist. Tiletamine hydrochloride exists as odourless white crystals.
Recreational use of Telazol has been documented.Animal studies have also shown that tiletamine produces rewarding and reinforcing effects. Tiletamine products are classified as Schedule III controlled substances in the United States.
Dosage:
If used alone the dose for sedation is 0.5 to 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.
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.
Quality Test Report:
Product Name | Tiletamine Hydrochloride | ||
CAS NO. | 14176-50-2 | Outer Packing | 1KG/Foil Bag |
Production Date | 2019-07-12 | Shelf Life | 2 years |
Standard | EP 8.0 | ||
Items of analysis | Specification | Results | |
Appearance | White crystals | White crystals | |
Loss on drying | ≤0.5% | 0.25% | |
Residue on ignition | ≤0.3% | 0.06% | |
Assay | ≥98% | 99% | |
Conclusion | Qualified |
1, High quality with competitive price:
1) Standard: U.S Standard
2) All Purity≥99.8%
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