Description

Morphine Phosphate is a critical pharmaceutical salt of the potent opioid analgesic, morphine, widely recognized under CAS NO 596-17-8. This compound is essential for the formulation of potent pain management medications, offering enhanced solubility and stability for precise therapeutic delivery. It is a fundamental active pharmaceutical ingredient (API) and intermediate for manufacturers in the pharmaceutical industry, particularly for producing injectable solutions, tablets, and controlled-release formulations for severe pain relief.

Application

• Pharmaceutical API: Primary use as the active ingredient in prescription analgesic medications for managing moderate to severe acute and chronic pain.
• Injectable Formulations: Key component in sterile injectable solutions for hospital and clinical use, including patient-controlled analgesia (PCA) pumps.
• Oral Solid Dosage Forms: Used in the production of immediate-release and extended-release tablets and capsules.
• Analytical Reference Standard: Serves as a high-purity standard in pharmaceutical quality control (QC) and research laboratories for HPLC, UV, and other analytical methods.
• Clinical Research: Utilized in preclinical and clinical studies investigating pain pathways, opioid efficacy, and new drug delivery systems.
• Veterinary Medicine: Employed in veterinary pharmaceuticals for pain management in animals.

Basic Information

Product Name	Morphine Phosphate
CAS No.	596-17-8
Molecular Formula	C17H21NO6 • H3PO4 • xH2O
Molecular Weight	Anhydrous: 433.37 g/mol (base + phosphate)
Synonyms	Morphine Phosphate Salt; Morphine Dihydrogen Phosphate; Morphinium Phosphate; Morphine Acid Phosphate; 7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol phosphate; Morfine Phosphate; Morphini Phosphas
EINECS	Contact for details

Quality Control

Our Morphine Phosphate is manufactured and tested under strict quality management systems. We offer grades suitable for pharmaceutical applications, with testing protocols aligned with industry pharmacopeial standards (e.g., USP, EP). Every batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles to ensure compliance with your specific requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water (KF)	≤ 6.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 2.0%
Microbial Limits	Meets Ph. Eur. 2.6.12 / USP <61> requirements

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