Description

Dextromoramide D-Tartrate CAS NO 23071-04-7 is a high-purity, synthetic opioid analgesic compound. It is a critical intermediate and reference standard in pharmaceutical research and development, particularly for the study of pain management pathways and receptor pharmacology. This material is essential for analytical laboratories, research institutions, and pharmaceutical companies engaged in method development, quality control, and advanced pharmacological studies.

Application

• Pharmaceutical Reference Standard: Used as a certified standard for the identification, purity assay, and quantification of dextromoramide in analytical methods such as HPLC, GC-MS, and NMR.
• Pharmacological Research: Serves as a key compound in preclinical studies investigating the mechanisms of opioid analgesia, receptor binding affinity, and structure-activity relationships (SAR).
• Analytical Method Development: Employed by QC/QA laboratories to develop, validate, and calibrate testing protocols for opioid-based active pharmaceutical ingredients (APIs) and finished dosage forms.
• Forensic Analysis: Utilized as a control substance in forensic toxicology for the accurate detection and confirmation of dextromoramide in biological samples.
• Chemical Synthesis Intermediate: Acts as a high-purity building block for the synthesis of novel chemical entities or labeled analogs for tracer studies.
• Regulatory Compliance & Documentation: Provides essential material for generating regulatory submission data, including stability studies and impurity profiling for drug master files (DMFs).

Basic Information

Product Name	Dextromoramide D-Tartrate
CAS No.	23071-04-7
Molecular Formula	C25H32N2O2 • C4H6O6
Molecular Weight	562.63 g/mol
Synonyms	Dextromoramide Tartrate; (+)-Moramide; Palfium; R-875; (R)-1-(3-Methyl-4-morpholino-2,2-diphenylbutyryl)pyrrolidine tartrate; 1-(3-Methyl-4-morpholino-2,2-diphenylbutyryl)pyrrolidine (2R,3R)-2,3-dihydroxysuccinate; Dextromoramide Bitartrate; NSC-114901
EINECS	Contact for details

Quality Control

Every batch of Dextromoramide D-Tartrate is manufactured under strict quality management systems and undergoes comprehensive analytical testing. We ensure compliance with stringent internal specifications suitable for research and development purposes. A detailed Certificate of Analysis (COA) providing data on identity, purity, and related substances is supplied with each shipment to guarantee traceability and product integrity.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white 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%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Specific Rotation	Contact for details

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