Tiletamine HCl CAS: 14176-50-2 Raw Powder

Tiletamine HCl CAS: 14176-50-2 Raw Powder China Steroid Raws/ Sarms/ Peptides sell on line. If you want to know more details, please contact Jason on: Email: jason168@yccreate.com WhatsApp:+8618042849221 Keywords: Tiletamine Hydrochloride; Tiletamine HCl; CAS: 14176-50-2 1. Product Introduction...

Product Details

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Tiletamine HCl CAS: 14176-50-2 Raw Powder

 

China Steroid Raws/ Sarms/ Peptides sell on line. If you want to know more details, please contact Jason on: Email: jason168@yccreate.com  WhatsApp:+8618042849221

 

Keywords: Tiletamine Hydrochloride; Tiletamine HCl; CAS: 14176-50-2

 

1. Product Introduction

Chemical name: Tiletamine Hydrochloride 
Synonyms: 2-(Ethylamino)-2-(2-thienyl)cyclohexanone Hydrochloride; CI 634; CL 399; CN 54521-2; NSC 167740; Tiletamin Hydrochloride;
CAS Number: 14176-50-2
Molecular form: C12H10ClNOS
Melting Point: 186-188°C (dec.)
Mol. Weight: 259.8
Mol File: 14176-50-2.mol
Appearance: White to Off-White Solid
Storage: Refrigerator, Under Inert Atmosphere
Solubility: DMSO, Methanol
Category; Amines, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds

Tiletamine HCl (2) 


2. Product 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.


3. Tiletamine HCl COA

Items of analysisSpecificationResults
CharacterOff-white to White Crystalline powderOff-White Crystalline powder
Solubilitysoluble in Ethanol (96%), Almost insoluble in DichloromethaneComplies
IdentificationSpecific Rotation -67-69.5° (on anhydrate basis)-67.4
Identification(2)IR:Meets the requirement.Complies
Identification(3)Optical purity TestComplies
Identification(4) Chloride ReactionComplies
ClarityClear,not deeper than Y6.Complies
PH2.8-3.42.9
Related SubstancesImpurity A≤0.15%0.03%
Related SubstancesImpurity B≤0.15%Not detected
Related SubstancesImpurity C ≤0.15%0.04%
Related SubstancesUnknown single impurity ≤0.15%0.07%
Related Substances0.1% Total Impurity≤0.5%0.18%
Impurity DImpurity D≤0. 5%0.05%
Water4.5%-6.5%5.7%
Heavy metals≤10ppmcomplies
Sulfate Ash≤0.1%0.04%
Assay99.0%~101.0%99.4%
ConclusionQualified


4. Tiletamine HCl Applications:

Tiletamine is a dissociative anesthetic and pharmacologically classified as an NMDA receptor antagonist.[1] It is related chemically to ketamine.[2] Tiletamine hydrochloride exists as odorless white crystals.
It is used in veterinary medicine in the combination product Telazol (tiletamine/zolazepam, 50 mg/ml of each in 5 ml vial) as an injectable anesthetic for use in cats and dogs.It is sometimes used in combination with xylazine (Rompun) to tranquilize large mammals such as polar bears and wood bison.
Telazol is the only commercially available tiletamine product in the United States. It is contraindicated in patients of an ASA score of III or greater and in animals with CNS signs, hyperthyroidism, cardiac disease, pancreatic or renal disease, pregnancy, glaucoma, or penetrating eye injuries.
Abuse 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.


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6. Order Process:

order


7. The quality control process:

1)Purchasing

Thorough market research, understand the price of raw materials and performance.To the procurement source to understand fully, and fully guarantee the quality of the procurement of raw materials.

2) Inspection

Four steps: sampling, sample pretreatment, measuring and data processing.

3) Producing

a)Each operator must do self-inspection of products and make the corresponding inspection records.

b)Full-time inspectors through check the operator self-inspection, and review and sign in the corresponding record. Full-time inspection is responsible for inspection of finished product, and make the finished product incoming inspection records.

4) Before selling 

Test result can be provided before selling.

Third-party detection institution is allowed if you are not satisfied with test results.


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