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Harm-reduction information only — not medical advice. In crisis or experiencing adverse effects, contact a healthcare professional or your local emergency services immediately.

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Anabolic Steroids/Hormones Human clinical data

Testosterone Base (Sublingual)

Sublingual T · Testoplek

37 min
Half-life
12.5–50 mg
Typical dose
2–3×/day
Frequency

Sublingual testosterone with extremely rapid peak and clearance; dosed multiple times daily.

Key takeaways

  • Ester-free T absorbed under the tongue; peak ~15 minutes, back to baseline within ~2 hours.
  • Human data exists only at 0.5 mg research doses; multi-mg protocols are anecdotal extrapolations.
  • Plotter half-life (~37 minutes) and 30% bioavailability are model estimates from that research.
  • Wide daily swings; bloodwork meaning depends on draw timing relative to dose.
🚧 Expanded guide coming soon. This compound has PK data and a source — a full overview, mechanism, and dosing guide is pending editorial review.

Reported dosing protocols

Protocols reported in research literature and clinic/community use — informational context, not a dosing recommendation.

Use case Dose Route Frequency Duration
Research (published) 0.5 mg, cyclodextrin-complexed Sublingual Single dose
Androgen replacement (community) 12.5–50 mg Sublingual 2–3× daily Ongoing

Pharmacokinetic summary

Model tier
Advanced (t½ + Cmax + Tmax + F)
Half-life
37 min
Cmax
800 ng/dL
Tmax
0.0 days
Bioavailability
30%
Typical dose
12.5–50 mg

Harm reduction

Aromatizes
Yes
DHT derivative
No
Injection frequency
2–3×/day

Frequently asked questions

Does sublingual testosterone actually work?

At raising serum testosterone for an hour or two, yes; that's documented. As a full replacement strategy, no evidence exists. The published studies used 0.5 mg for acute effects in women, which says nothing about holding eugonadal levels all day.

Why not just swallow it?

Swallowed testosterone is destroyed by first-pass liver metabolism before it reaches circulation. The oral products that work (oral testosterone undecanoate) absorb through the lymphatics instead. Sublingual dosing dodges the liver via the oral mucosa, briefly.

Is the 30% bioavailability figure reliable?

It's an estimate from small acute-dose studies, not a validated parameter. Real absorption depends on formulation (cyclodextrin complex vs raw base), contact time under the tongue, and how much gets accidentally swallowed.

References

Related compounds

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