Description

S-(-)-Aminoglutethimide D-Tartrate Salt is a high-purity, enantiomerically pure salt form of the pharmaceutical compound aminoglutethimide. This specific stereoisomer is critical for research and development activities where precise molecular configuration dictates biological activity and metabolic pathways. It is primarily utilized by pharmaceutical R&D laboratories, academic research institutions, and fine chemical manufacturers engaged in developing and producing specialized active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Research & Development: Serves as a key chiral intermediate or reference standard in the synthesis and study of novel therapeutic agents, particularly in oncology and endocrinology.
• Active Pharmaceutical Ingredient (API) Manufacturing: Used in the controlled production of enantiomerically pure drug substances where the S-(-)-enantiomer is the therapeutically active form.
• Biochemical Research: Employed as a selective inhibitor in enzymatic and receptor-binding studies to investigate steroidogenesis and related metabolic pathways.
• Analytical Reference Standard: Provides a certified material for quality control laboratories to validate analytical methods like HPLC and LC-MS for potency and purity assessments.
• Preclinical Studies: Utilized in pharmacological and toxicological evaluations to understand the efficacy and safety profile of the specific enantiomer.

Basic Information

Product Name	S-(-)-Aminoglutethimide D-Tartrate Salt
CAS No.	57288-04-7
Molecular Formula	C13H16N2O2 • C4H6O6
Molecular Weight	406.38 g/mol
Synonyms	(S)-(-)-Aminoglutethimide D-Tartrate; (3S)-3-(4-Aminophenyl)-3-ethylpiperidine-2,6-dione D-Tartrate; S-Aminoglutethimide Tartrate; (-)-Aminoglutethimide D-Tartrate Salt; AGT D-Tartrate; (S)-AG Tartrate; (S)-3-(4-Aminophenyl)-3-ethyl-2,6-piperidinedione D-Tartrate
EINECS	Contact for details

Quality Control

Our S-(-)-Aminoglutethimide D-Tartrate Salt is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity assay, identification, and impurity profiling, to ensure it meets stringent specifications for research and pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Chiral Purity (HPLC)	≥99.0% (S-Enantiomer)
Loss on Drying	≤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.