Description

Dextromoramide Tartrate is a potent synthetic opioid analgesic compound. Its primary value lies in its application as a high-potency active pharmaceutical ingredient (API) for research and development within the pharmaceutical sector. This compound is essential for organizations involved in the development of analgesic medications, neuropharmacological research, and controlled substance studies. Dextromoramide Tartrate CAS NO 3528-84-5 is handled under strict regulatory frameworks due to its pharmacological profile.

Application

• Pharmaceutical Research & Development (R&D): Serves as a key reference standard and active ingredient in the development of novel analgesic formulations.
• Analgesic Pharmacology Studies: Used in preclinical and clinical research to study opioid receptor interactions, efficacy, and metabolic pathways.
• Chemical Reference Standard: Employed in analytical laboratories for method development, validation, and quality control testing of pharmaceutical products.
• Neuropharmacology: A tool compound for investigating pain management mechanisms within the central nervous system.
• Controlled Substance Analysis: Utilized by forensic and regulatory laboratories for calibration and identification purposes in substance analysis programs.

Basic Information

Product Name	Dextromoramide Tartrate
CAS No.	3528-84-5
Molecular Formula	C₂₅H₃₂N₂O₂ • C₄H₆O₆
Molecular Weight	542.6 g/mol
Synonyms	Dextromoramide Tartrate; (+)-1-(3-Methyl-4-morpholino-2,2-diphenylbutyryl)pyrrolidine tartrate; Palfium; Jetrium; Dimorlin; R-875; Pyrrolamidol; Dextromoramidum; NSC-114901; Moramide intermediate
EINECS	Contact for details

Quality Control

Our Dextromoramide Tartrate is manufactured and handled under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. Specifications are aligned with pharmacopeial standards where applicable. A detailed Certificate of Analysis (COA) documenting purity, related substances, residual solvents, and other critical parameters is provided with every shipment to ensure full traceability and compliance for your research needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Loss on Drying	≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines

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