Oxandrolone (Anavar) Pills

Price range: $33.00 through $52.00

Comprehensive Chemical Information and Composition

Formulating a stable, high-purity batch of oxandrolone (anavar) pills requires absolute precision in organic synthesis, stereochemical control, excipient selection, and analytical verification. Whether supplied as raw crystalline powder or manufactured into precisely dosed research tablets, understanding its exact chemical identity is paramount for laboratory quality control.

Molecular and Chemical Specifications:

  • International Nonproprietary Name / Research Identifiers: Oxandrolone, Anavar, Lonavar, Vasculit
  • IUPAC Chemical Name: (5α,17β)-17-hydroxy-17-methyl-2-oxaandrostane-3-one
  • Base Chemical Formula: C19H30O3
  • Molecular Weight: 306.44 g/mol
  • Purity Standards: Exceeding 99% verified via High-Performance Liquid Chromatography (HPLC) and Mass Spectrometry (MS).
  • Physical State: Fine crystalline powder (API) compressed into uniform pharmaceutical-grade oral tablets (pills).

Core Structural Features

The chemical architecture of oxandrolone (anavar) is characterized by a modified dihydrotestosterone (DHT) core featuring three monumental structural alterations that completely govern its biological behavior:

  1. The A-Ring Heterocyclic Substitution (2-Oxa modification): Unlike standard steroid nuclei that feature a purely carbon-based A-ring, oxandrolone (anavar) is characterized by the substitution of carbon-2 with an oxygen atom. This 2-oxa modification alters the electronic conformation of the steroid core, drastically increasing its resistance to enzymatic reduction by skeletal muscle 3-alpha hydroxysteroid dehydrogenase enzymes and enhancing its relative anabolic potency.
  2. C17-alpha Alkylation: The addition of a methyl group at the 17th carbon position protects the hormone from immediate breakdown during first-pass hepatic metabolism. Without this C17-alpha alkylation, oral ingestion of DHT derivatives results in virtually 0% systemic bioavailability due to rapid destruction by liver enzymes. In oxandrolone (anavar), this methylation ensures that the active compound enters systemic circulation intact.
  3. 17-beta Hydroxyl Group: The retention of the 17-beta hydroxyl group allows the molecule to interact effectively with androgen receptors while maintaining stability across variable physiological pH levels.