Description

Amustaline Dihydrochloride is a high-purity chemical compound of significant interest in advanced pharmaceutical research and development. This compound serves as a critical intermediate or active pharmaceutical ingredient (API) in the synthesis of novel therapeutic agents. It is primarily utilized by research institutions and pharmaceutical companies engaged in the development of new drug candidates, particularly within specialized therapeutic areas. Our supply ensures consistent quality and reliable availability for your critical projects.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel active pharmaceutical ingredients (APIs) for preclinical and clinical research.
• Biochemical Research: Used as a reference standard or reagent in studies investigating specific biological pathways and mechanisms of action.
• Drug Discovery & Development: Employed in high-throughput screening and medicinal chemistry programs to identify and optimize new drug candidates.
• Analytical Standard: Serves as a certified reference material for quality control and analytical method development in pharmaceutical laboratories.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP-compliant production of investigational drugs.

Basic Information

Product Name	Amustaline Dihydrochloride
CAS No.	210584-54-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Amustaline HCl; Amustaline Hydrochloride; 1,3-Dihydroxypropan-2-yl 4-[(2-amino-9H-purin-9-yl)methyl]benzoate dihydrochloride; 4-[(2-Amino-9H-purin-9-yl)methyl]benzoic acid 1,3-dihydroxy-2-propyl ester dihydrochloride; Amustaline (dihydrochloride); UNII-9H8P7D6S2K
EINECS	Contact for details

Quality Control

Our Amustaline Dihydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, to ensure it meets the stringent requirements for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with agreed specifications.

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). This product is hygroscopic (moisture-sensitive) and must be kept under dry conditions to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%

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