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(+-)-Methadone Hydrochloride--Dea CAS NO 125-56-4


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CAS No.:125-56-4

Grade:Pharmacy Grade

Content:99.0%

Brand:Customizable

Packaging:Customizable

Description

(+-)-Methadone Hydrochloride--Dea CAS NO 125-56-4 is a synthetic opioid analgesic and a key pharmaceutical active ingredient. It is a critical compound for the production of controlled medication used in pain management and addiction treatment programs. This high-purity substance is essential for pharmaceutical manufacturers, analytical reference standard producers, and research institutions developing therapeutic protocols.

Application

  • Pharmaceutical Active Ingredient (API): Primary use in the formulation of methadone-based medications for severe pain management.
  • Opioid Dependence Treatment: A cornerstone component in Medication-Assisted Treatment (MAT) programs for opioid use disorder.
  • Analytical Reference Standard: Used in forensic, clinical, and pharmaceutical laboratories for qualitative and quantitative analysis (e.g., HPLC, GC-MS).
  • Clinical Research & Development: Serves as a key reagent in pharmacological studies and the development of new analgesic formulations.
  • Controlled Substance Manufacturing: Supplied to licensed facilities for the production of DEA-scheduled pharmaceutical products.

Basic Information

Product Name (+-)-Methadone Hydrochloride--Dea CAS NO 125-56-4
CAS No. 125-56-4
Molecular Formula C21H27NO • HCl
Molecular Weight 345.91 g/mol
Synonyms Methadone HCl; (±)-Methadone Hydrochloride; DL-Methadone Hydrochloride; 6-(Dimethylamino)-4,4-diphenyl-3-heptanone Hydrochloride; Amidon Hydrochloride; Phenadone Hydrochloride; Heptadon Hydrochloride; EINECS 204-754-5
EINECS 204-754-5

Quality Control

Our (+-)-Methadone Hydrochloride is manufactured under strict quality systems to ensure it meets the exacting standards required for pharmaceutical and analytical use. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant Good Manufacturing Practice (GMP) principles where applicable, and the product is suitable for use as a pharmaceutical reference standard.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment. Keep the container tightly sealed when not in use to prevent degradation.

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% (on anhydrous basis)
Water (KF) ≤ 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.

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