Description

Drinamyl is a pharmaceutical-grade active ingredient, identified by CAS No. 8065-31-4. This compound is valued for its specific therapeutic properties and is manufactured under strict quality control to ensure batch-to-batch consistency and regulatory compliance. It is primarily required by the pharmaceutical industry for the formulation of prescription medications.

Application

• Pharmaceutical Formulations: As a key active pharmaceutical ingredient (API) in solid and liquid dosage forms.
• Central Nervous System (CNS) Medications: Used in the development of treatments targeting specific neurological pathways.
• Generic Drug Manufacturing: Serves as a critical component for producing cost-effective generic versions of established therapies.
• Clinical Research & Development: Employed in preclinical and clinical studies for new therapeutic applications.
• Contract Manufacturing Organizations (CMOs): Supplied to CMOs for the production of finished drug products for various markets.

Basic Information

Product Name	Drinamyl
CAS No.	8065-31-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Dexamyl; Amobarbital and Dextroamphetamine; Amobarbital-Dextroamphetamine Combination; Barbiturate-Amphetamine Combination; Trankimazin (in some contexts); CNS Stimulant-Depressant Combination
EINECS	Contact for details

Quality Control

Our Drinamyl is produced in facilities adhering to cGMP (current Good Manufacturing Practice) guidelines. Every batch undergoes rigorous analytical testing to ensure identity, purity, strength, and composition. Certificates of Analysis (COA) documenting compliance with relevant pharmacopoeial standards (such as USP or in-house specifications) are available upon request to support your regulatory filings.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials and sources of ignition.

Specification

Item	Specification
Appearance	White to off-white powder or solid
Identification (IR)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 0.1%

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