Description

Hypnorm is a potent synthetic opioid analgesic agent used primarily in veterinary medicine. This compound is critical for providing effective and reliable sedation and pain management in animals, particularly during surgical procedures or diagnostic examinations. It is an essential pharmaceutical active ingredient for veterinary clinics, research institutions, and animal health product manufacturers requiring a controlled, high-purity substance for formulation.

Application

• Veterinary Anesthesia & Sedation: Primary use as a pre-anesthetic medication or for chemical restraint in a wide range of animal species.
• Analgesia in Veterinary Surgery: Provides potent pain relief as part of balanced anesthetic protocols for surgical interventions.
• Immobilization of Wildlife: Used in wildlife management and conservation for the safe capture and handling of large or exotic animals.
• Veterinary Pharmaceutical Manufacturing: Serves as the active pharmaceutical ingredient (API) in the production of injectable sedative and analgesic formulations.
• Veterinary Research & Development: Employed in preclinical studies and pharmacological research within animal health sciences.

Basic Information

Item	Detail
Product Name	Hypnorm
CAS No.	52869-98-4
Molecular Formula	C₂₃H₃₀FN₃O
Molecular Weight	383.50 g/mol
Synonyms	Fentanyl citrate; Fentanyl; Phentanyl; Sublimaze; Duragesic; Actiq; Fentanil; (±)-Fentanyl; N-(1-Phenethyl-4-piperidyl)propionanilide citrate; 1-Phenethyl-4-(N-phenylpropionamido)piperidine citrate
EINECS	Contact for details

Quality Control

Our Hypnorm is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and the absence of specified impurities. We adhere to cGMP principles where applicable to ensure consistent quality and traceability.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container securely sealed in a well-ventilated area away from incompatible materials. Due to its potency and controlled substance status, ensure storage complies with all local and international regulations for narcotic drugs.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.