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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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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






