Description

Amphetamine Aspartate is a pharmaceutical-grade salt form of amphetamine, a potent central nervous system stimulant. This specific compound is critical for ensuring precise dosage, stability, and bioavailability in controlled therapeutic formulations. It is primarily required by manufacturers in the pharmaceutical industry for the development and production of prescription medications.

Application

• Active Pharmaceutical Ingredient (API) in prescription stimulant medications.
• Key intermediate in the synthesis of specialized neuropharmacological agents.
• Reference standard for quality control and analytical testing in pharmaceutical laboratories.
• Research and development of treatments for attention deficit hyperactivity disorder (ADHD).
• Component in clinical research studies investigating central nervous system disorders.
• Manufacturing of controlled-release dosage forms for regulated therapeutic use.

Basic Information

Product Name	Amphetamine Aspartate
CAS No.	25333-81-7
Molecular Formula	C9H13N • C4H7NO4
Molecular Weight	368.41 g/mol
Synonyms	Dextroamphetamine Aspartate; (S)-1-Phenylpropan-2-amine (2S)-2-aminobutanedioate; Amphetamine D-Aspartate; Dexamphetamine Aspartate; Aspartic Acid, Amphetamine Salt; (±)-Amphetamine Aspartate; ADDERALL component; Dextroamphetamine Hydrogen Aspartate
EINECS	Contact for details

Quality Control

Our Amphetamine Aspartate is manufactured under strict quality management systems. The product undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each batch to ensure regulatory compliance and traceability.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Optical Rotation	Specific range provided on COA

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