Description

Piperazine Succinate is a high-purity organic salt formed from piperazine and succinic acid, offering a stable and bioavailable form of the active moiety. This compound is valued for its consistent quality and reliable performance in critical synthesis and formulation processes. It serves as a key intermediate and active pharmaceutical ingredient (API) in the pharmaceutical industry, particularly for the development of anthelmintic and other therapeutic agents.

Application

• Pharmaceutical Intermediate: A crucial building block in the synthesis of various piperazine-derived active pharmaceutical ingredients (APIs).
• Anthelmintic Drug Production: Used in the manufacture of medications for treating parasitic worm infections.
• Chemical Synthesis: Serves as a reagent or starting material in organic chemistry for creating complex molecules.
• Biochemical Research: Employed in laboratory research as a standard or buffer component in specific biochemical studies.
• Veterinary Medicine: A component in formulations for animal health products targeting parasites.

Basic Information

Product Name	Piperazine Succinate
CAS No.	14396-13-5
Molecular Formula	C8H16N2O4
Molecular Weight	204.22 g/mol
Synonyms	Piperazine Succinate; Piperazine, Succinate (1:1); Piperazine Succinate Salt; Piperazine Monosuccinate; 1,4-Diazacyclohexane Succinate; Diethylenediamine Succinate; Succinic Acid Piperazine Salt; UNII-7J3K385C1W
EINECS	Contact for details

Quality Control

Our Piperazine Succinate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are provided with every shipment to guarantee traceability and compliance with your 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). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
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%

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