Description

Tramadol CAS NO 73806-55-0 is a centrally acting synthetic opioid analgesic. It is a critical active pharmaceutical ingredient (API) valued for its effectiveness in managing moderate to moderately severe pain. This compound is essential for pharmaceutical manufacturers producing generic and branded analgesic medications. Our supply ensures high purity and reliable consistency for formulation development and commercial production.

Application

• Pharmaceutical API: Primary use as the active ingredient in immediate-release and extended-release oral tablets and capsules for pain management.
• Generic Drug Formulation: Sourcing for the production of bioequivalent generic versions of tramadol hydrochloride medications.
• Combination Analgesics: Used in fixed-dose combination products with other analgesics like acetaminophen for enhanced therapeutic effect.
• Clinical Research: Serves as a reference standard and raw material in pharmacokinetic and pharmacodynamic studies.
• Veterinary Medicine: Application in formulated products for the management of pain in animals under veterinary supervision.

Basic Information

Product Name	Tramadol
CAS No.	73806-55-0
Molecular Formula	C16H25NO2
Molecular Weight	263.38 g/mol
Synonyms	Tramadol Base; (±)-Tramadol; (1R*,2R*)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol; Trancodal; Ultram (as hydrochloride salt); CG 315; K 315; Zydol
EINECS	Contact for details

Quality Control

Our Tramadol is manufactured and tested to meet stringent pharmacopeial standards. Quality assurance protocols ensure compliance with relevant monographs such as USP, EP, and BP. Every batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We are committed to supplying material that supports our clients' regulatory filings and GMP manufacturing requirements.

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). This material is hygroscopic (moisture-sensitive) and must be kept under conditions that minimize exposure to atmospheric humidity.

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.5% - 101.0% (on anhydrous basis)
Water (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity: ≤ 0.15% Total impurities: ≤ 0.5%
Heavy Metals	≤ 20 ppm

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