Description

Spasmo-Eunalgit is a high-purity pharmaceutical intermediate and active ingredient with the CAS registry number 138230-24-7. This compound is critical for the synthesis of specialized therapeutic agents, offering reliable performance and consistent quality for demanding manufacturing processes. It is primarily utilized by the pharmaceutical and life sciences industries for research and development, as well as commercial production of targeted medications.

Application

• Pharmaceutical Synthesis: Key intermediate in the production of antispasmodic and analgesic drug formulations.
• Active Pharmaceutical Ingredient (API): Serves as a core component in finished dosage forms for targeted therapeutic applications.
• Biochemical Research: Used in pharmacological studies and as a reference standard in analytical method development.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for scale-up and commercial production.
• Veterinary Medicine: Potential application in the development of veterinary pharmaceuticals.

Basic Information

Item	Details
Product Name	Spasmo-Eunalgit
CAS No.	138230-24-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	138230-24-7; Spasmo Eunalgit; Eunalgit; SpasmoEunalgit; (Chemical name based on CAS); (IUPAC name based on CAS); (Common pharmaceutical intermediate name)
EINECS	Contact for details

Quality Control

Our Spasmo-Eunalgit is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent purity and identity specifications, typical for pharmaceutical-grade intermediates. A Certificate of Analysis (COA) detailing purity, impurities, and other critical parameters is provided with every shipment to guarantee traceability and compliance.

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). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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