SARMs

Ibutamoren MK-677 20 mg Swiss Pharmaceuticals

Swiss Pharmaceuticals

70,00

In Stock (100 available)

Ibutamoren MK-677 20 mg Swiss Pharmaceuticals (20 mg) — Backed by Swiss Pharmaceuticals’s commitment to quality, an oral growth hormone secretagogue that stimulates the pituitary gland t…

100 in stock

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

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Description

Ibutamoren MK-677 20 mg Swiss Pharmaceuticals — ibutamoren (MK-677) from Swiss Pharmaceuticals at 20 mg. Oral GH secretagogue mimicking ghrelin — pulsatile GH release following physiological rhythm rather than bolus injection.

Key Benefits

  • Oral GH secretagogue — raises endogenous GH and IGF-1
  • Sleep quality, appetite, recovery improvements
  • Does not suppress HPTA
  • Long-run compound — 3–6 month commitment for full effect
  • Water retention common in first month
  • Each unit dosed at 20 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Research dosing: 10–25 mg/day, single oral dose pre-bed (sleep benefit) or split. Cycles 3–6 months for full recomposition effect.

How It Works

Ibutamoren, ghrelin-receptor agonist. Triggers endogenous GH pulse release from the pituitary, elevates IGF-1. Mechanism distinct from exogenous HGH — works on the physiological pulse pathway.

Pharmacokinetics

Plasma half-life approximately 24 hours. Single daily dose produces stable GH/IGF-1 elevation.

Potential Side Effects

Water retention first month (resolves). Insulin resistance risk on long runs — monitor fasting glucose. Appetite increase. Mild lethargy in a minority of users.

Cycle & Stacking Guide

3–6 month protocols. Stacks cleanly with SARMs or AAS cycles for recovery amplification. Store pills dry and cool.

Manufacturer Notes

Swiss Pharmaceuticals is a research-compound producer with published batch QC data. Vials ship with tamper-evident caps and date-coded labels.

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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Mk 677

Physical & Chemical Properties for Research Purposes
Chemical structure of Mk 677 (C27H36N4O5S) for laboratory analysis
2D structural representation · PubChem CID 9918102 ↗
Chemical Identity
# CAS Registry Number 159752-10-0
Σ IUPAC Name 2-amino-2-methyl-N-[(2R)-1-[methyl-[(2R)-1-(1-methanesulfonylspiro[2,3-dihydroindole-3,4'-piperidine]-1'-yl)-1-oxo-3-phenylmethoxypropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]propanamide
F Molecular Formula C27H36N4O5S
M Molecular Weight 528.66 g/mol
SMILES CC(C)(N)C(=O)N[C@H](C(=O)N(C)[C@@H](COCC1=CC=CC=C1)C(=O)N2CCC3(CC2)C(N(C4=CC=CC=C34)S(C)(=O)=O))CC5=CC=CC=C5
InChIKey XBWOXCUWQMFQQV-HNZIOWRTSA-N
Melting Point 153-155 °C
Solubility Soluble in DMSO, ethanol; poorly soluble in water
Biological Half-life 24 hours (oral)
PubChem CID 9918102 ↗
Pharmacological Profile
Aromatization None
Hepatotoxicity Low
Known trade names: Ibutamoren, MK-677, Nutrobal

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