
Orals
Turinabol 10mg
Chlorodehydromethyltestosterone, a balanced oral anabolic studied for lean gains without water retention.
Turinabol (Chlorodehydromethyltestosterone) is an oral anabolic steroid derived from the Dianabol backbone, engineered to remove its oestrogenic activity while retaining useful anabolic properties. This 10mg tablet strength is supplied 100 per tub. Structurally classified as C17H21ClN2O2, Turinabol combines a chlorine substitution with modifications to the parent steroid, resulting in a compound favoured in research for balanced bulking and cutting applications alike, with an anabolic-to-androgenic dissociation notable enough that it earned the nickname "mild Dianabol" in the research literature. With a half-life of approximately 16 hours, Turinabol supports steady blood levels across a research protocol. Like other 17-alpha-alkylated orals, it is studied for a meaningful negative effect on lipid markers (raising LDL, lowering HDL) despite lacking oestrogenic activity — its "mild" reputation applies to androgenic side effects, not lipid or hepatic strain.
Independent laboratory documentation
Certificates of Analysis
View the laboratory reports currently published for this product.
Certificate of Analysis
Specifications
Research Benefits
- Balanced Anabolic Effects — Studied for delivering steady lean gains suited to both bulking and cutting research.
- No Aromatisation — The chlorine substitution prevents conversion to oestrogen, avoiding water retention.
- Lean Tissue Quality — Associated with dry, quality muscle gains rather than rapid water-driven mass.
- Favourable Anabolic:Androgenic Split — Regarded in the literature as delivering anabolic effects with comparatively low androgenic activity, earning it the nickname "mild Dianabol".
- Stable Blood Levels — A 16-hour half-life supports steady, once or twice-daily research dosing.
How It Works
Because it does not convert to oestrogen, research models report an absence of water retention. Its 17-alpha-alkylation — the same structural feature that gives it oral bioavailability — is studied for a negative effect on lipid markers similar to other 17-aa orals, so its "mild" profile refers specifically to androgenic side effects rather than lipid or hepatic strain. The 16-hour half-life allows for consistent circulating levels across a dosing protocol.
⚠ For Research Use Only
By purchasing, the buyer confirms this product is being acquired for legitimate research purposes and assumes full responsibility for its handling, storage, and use in compliance with all applicable local, national, and international laws.
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