Description

Iso Methadone CAS NO 6293-01-2 is a synthetic opioid compound of significant interest in pharmaceutical research and development. This compound serves as a key intermediate or reference standard in the synthesis and analytical profiling of active pharmaceutical ingredients (APIs) and their metabolites. It is primarily utilized by research institutions, pharmaceutical manufacturers, and analytical laboratories engaged in neuropharmacology, pain management research, and forensic toxicology. Our supply is characterized by high purity and batch-to-batch consistency to meet the stringent demands of scientific and industrial applications.

Application

• Pharmaceutical Reference Standard: Used as an analytical standard in HPLC, GC-MS, and NMR for method development, validation, and quality control of related pharmaceutical products.
• Chemical Intermediate: Serves as a critical building block in the organic synthesis of novel opioid analogs and related therapeutic compounds for research purposes.
• Metabolite Studies: Employed in pharmacokinetic and metabolic pathway research to study the biotransformation and disposition of opioid substances.
• Forensic Analysis: Utilized as a calibrant or control substance in forensic laboratories for the accurate identification and quantification of opioids in biological samples.
• Pharmacological Research: Applied in in-vitro and in-vivo studies to investigate receptor binding affinity, efficacy, and structure-activity relationships (SAR) within the opioid receptor family.

Basic Information

Item	Detail
Product Name	Iso Methadone
CAS No.	6293-01-2
Molecular Formula	C21H27NO
Molecular Weight	309.45 g/mol
Synonyms	iso-Methadone; (R*,S*)-6-(Dimethylamino)-4,4-diphenyl-3-heptanone; dl-iso-Methadone; (±)-iso-Methadone; NSC 179434; 3-Heptanone, 6-(dimethylamino)-4,4-diphenyl-, (±)-; Racemic iso-Methadone
EINECS	Contact for details

Quality Control

Our Iso Methadone is manufactured under controlled conditions and subjected to rigorous analytical testing to ensure identity, purity, and consistency. Each batch is supported by a comprehensive Certificate of Analysis (COA) detailing key parameters such as assay, impurity profile, and residual solvents. We adhere to cGMP principles where applicable, and our quality systems are designed to meet the exacting standards of the pharmaceutical and research industries. Certificates of Analysis are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture. Store away from incompatible materials.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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