Description

Teludipine is a high-purity pharmaceutical intermediate and research chemical, identified by CAS NO 108700-30-7. It serves as a critical building block in the synthesis of advanced active pharmaceutical ingredients (APIs), particularly in the cardiovascular therapeutic area. This compound is essential for pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in medicinal chemistry and drug discovery programs.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of dihydropyridine-class calcium channel blockers and related cardiovascular drugs.
• Medicinal Chemistry Research: Used as a scaffold or reference standard in structure-activity relationship (SAR) studies and novel drug candidate development.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex molecules with specific chiral or functional group properties.
• Analytical Reference Standard: Serves as a high-purity standard for quality control (QC) and analytical method development (e.g., HPLC, LC-MS) in pharmaceutical manufacturing.
• Biochemical Research: Utilized in pharmacological studies to investigate ion channel modulation and related cellular mechanisms.

Basic Information

Product Name	Teludipine
CAS No.	108700-30-7
Molecular Formula	C19H21N3O6
Molecular Weight	387.39 g/mol
Synonyms	Teludipine; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 3-methyl 5-(1-methylethyl) ester; Isopropyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate; 4-(3-Nitrophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-methyl 5-(1-methylethyl) ester; (±)-Teludipine
EINECS	Contact for details

Quality Control

Our Teludipine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and support our products with detailed Certificates of Analysis (COA). Specifications are designed to meet the stringent requirements of pharmaceutical R&D and cGMP intermediate applications.

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. For long-term storage, consider inert atmosphere conditions to maintain optimal stability.

Specification

Item	Specification
Appearance	Yellow to light brown crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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