SARMs

MK 2866 (Ostarine) 10 mg Elbrus Pharmaceuticals

Elbrus Pharmaceuticals

65,00

In Stock (100 available)

MK 2866 (Ostarine) 10 mg Elbrus Pharmaceuticals (10 mg) — This Elbrus Pharmaceuticals formulation delivers the most extensively researched and versatile SARM (Selective Androgen Receptor M…

100 in stock

This product is for laboratory research use only. Not for human consumption.

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Description

MK 2866 (Ostarine) 10 mg Elbrus Pharmaceuticals — ostarine (MK-2866) from Elbrus Pharmaceuticals at 10 mg. Selective androgen receptor modulator — tissue-targeted for muscle and bone. Milder HPTA suppression than anabolic steroids.

Key Benefits

  • Most-studied SARM — extensive clinical trial data
  • Low suppression at 10–15 mg/day — recovery often possible without PCT
  • Cutting recomp compound — lean mass in caloric deficit
  • Oral once-daily dosing
  • Starting compound for SARM-curious users
  • Each unit dosed at 10 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Research dosing: 10–25 mg/day for 8 weeks. Women 5–10 mg/day. Single daily dose adequate given long half-life. Cycles 8–12 weeks. Doses above 25 mg/day suppression becomes meaningful.

How It Works

MK-2866, selective androgen receptor modulator. Binds the AR with tissue selectivity: high activity in muscle and bone, low activity in prostate and skin. Downstream anabolic effects without the full androgenic profile of AAS.

Pharmacokinetics

Plasma half-life approximately 24 hours. Once-daily dosing sufficient. Steady-state in 5 days.

Cycle & Stacking Guide

Beginner SARM cycle: 10–15 mg/day × 8 weeks. Mild mini-PCT (Nolva 20 mg/day × 4 weeks) if bloodwork confirms suppression. Stacks with cardarine for recomp or with TRT for lean gains.

Manufacturer Notes

Elbrus Pharmaceuticals is an Eastern European producer with GMP certification. Their pharmacology catalogue is broad, covering AAS, peptides, and harm-reduction supports.

Storage & Handling

Store in the original blister or bottle at 15–25 °C, away from direct sunlight, heat, and humidity. Oral preparations lose potency faster if exposed to moisture; keep the desiccant (if included) with the tablets. Keep out of reach of children. For research and educational purposes only.

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Ostarine

Physical & Chemical Properties for Research Purposes
Chemical structure of Ostarine (C19H14F3N3O3) for laboratory analysis
2D structural representation · PubChem CID 11326715 ↗
Chemical Identity
# CAS Registry Number 841205-47-8
Σ IUPAC Name (2S)-3-(4-cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide
F Molecular Formula C19H14F3N3O3
M Molecular Weight 389.33 g/mol
SMILES C[C@@](O)(COC1=CC=C(C=C1)C#N)C(=O)NC2=CC(=C(C=C2)C#N)C(F)(F)F
InChIKey JKUYRFLXQDGHBQ-INIZCTEOSA-N
Melting Point 132-136 °C
Solubility Soluble in DMSO, ethanol; practically insoluble in water
Biological Half-life 24 hours (oral)
PubChem CID 11326715 ↗
Pharmacological Profile
Anabolic Rating N/A (non-steroidal)
Androgenic Rating N/A (tissue-selective)
Aromatization None
Hepatotoxicity Low
Detection Time 4 weeks
Known trade names: Ostarine, MK-2866, Enobosarm, GTx-024

Data sourced from published pharmacological literature and authoritative chemical databases (PubChem, DrugBank, ChEBI). Provided for identification and research reference only.