RAD-150 (TLB-150)
Also known as: RAD-150, TLB-150, TLB150, Testolone benzoate, RAD150
Sold as an esterified RAD-140 with a longer duration. The chemistry is plausible, the evidence is nonexistent, and even the identity of what is sold is unverified.
Substance family
Non-steroidal compounds binding the same androgen receptor as testosterone, but favouring muscle and bone over prostate and hair. The selectivity is real; the suppression of the body's own production is not avoided by it. None is approved anywhere.
Effects on
Which outcomes this substance acts on — descriptive, not a recommendation.
Strain profile
Where this substance is most likely to hit — a rough orientation, individually dependent on dose, duration and predisposition.
This substance causes
Dosing & protocols by goal
Rough orientation ranges as reported in harm-reduction literature — not an individual treatment plan. Doses are individual and open-ended; frequency depends on the ester or half-life.
Research data
MedicalDose
Does not exist
Frequency
—
Cycle length
—
Unlike the other compounds in this category, RAD-150 has no research record at all — not even preclinical. It appeared on the grey market rather than emerging from a development programme.
Grey market practice
Not a recommendationDose
10–20 mg / day reported
Frequency
1× daily
Cycle length
6–8 weeks reported
Figures copied from RAD-140 dosing. Whether they transfer to an esteresterA chemical chain attached to a steroid to slow its release from the injection site. with different release kinetics is unknown, and would depend on the ester actually being present.
Side effect & countermeasure
Typical problems and what you can do to reduce harm — at a glance. Does not replace medical monitoring.
Problem
The identity of what is sold is unverified
Countermeasure
RAD-150 is described as testolone benzoate — RAD-140 with a benzoate esteresterA chemical chain attached to a steroid to slow its release from the injection site. attached. That is chemically coherent, and it is also the entire basis for the product. There is no published synthesis, no characterisation, no pharmacokinetic data. Independent analyses of products sold as RAD-150 have found plain RAD-140. Someone buying this may simply be paying more for the compound they could have bought directly.
Problem
Esterification does not work the same way orally
Countermeasure
The esteresterA chemical chain attached to a steroid to slow its release from the injection site. concept comes from injectable steroids, where the ester slows release from an oil depot in muscle. That mechanism requires a depot. An oral ester is cleaved in the gut and liver, and whether it meaningfully extends duration depends entirely on the specific chemistry — which has not been measured here. The marketing borrows the logic of injectable esters without the mechanism that makes it work.
Problem
It carries RAD-140's risks by design
Countermeasure
If the product is what it claims, it delivers RAD-140. That means the same strong suppressionsuppressionThe body shutting down its own testosterone production because an external source is present., the same effect on lipids and the elevated liver values that RAD-140 users report — including several published case reports of drug-induced liver injury. Nothing about adding an esteresterA chemical chain attached to a steroid to slow its release from the injection site. reduces those.
Problem
Severe suppression
Countermeasure
RAD-140 is among the more suppressivesuppressiveThe body shutting down its own testosterone production because an external source is present. SARMsSARMsA non-steroidal compound that binds the androgen receptor with claimed tissue selectivity., and an esteresterA chemical chain attached to a steroid to slow its release from the injection site. intended to extend exposure does not soften that. PCTPCTThe protocol after a cycle intended to restart the body's own testosterone production. with enclomiphene or clomiphene, bloodwork before and after.
Overview
RAD-150 is the newest entry in this category and the one with the least behind it. It differs from every other compound on these pages in an important way: it did not come from a research programme at all.
Ostarine, LGD-4033, andarine, S-23, ACP-105 and the rest are real compounds with development histories, however incomplete. RAD-150 appeared on the grey market as a product.
What It Is Claimed To Be
The description is that RAD-150 — also sold as TLB-150 — is RAD-140 with a benzoate ester attached, producing a longer duration of action and more stable blood levels.
The chemistry of that idea is coherent. Esterification is a real and well-understood technique, and it is exactly how testosterone enanthate and trenbolone acetate work.
What is missing is everything else. There is no published synthesis, no characterisation data, no pharmacokinetic study, no measurement of half-life confirming the longer duration. There is a product description.
The Problem With Borrowing Ester Logic
The ester concept comes from injectables. An oil-based steroid sits in a muscle depot, enzymes cleave the ester off gradually, and the active compound releases slowly. The depot is essential to the mechanism.
An oral compound has no depot. It is absorbed through the gut and passes through the liver, where esters are cleaved rapidly. Whether an oral ester meaningfully extends duration depends on specific properties that would have to be measured — and here they have not been.
So the claim uses the vocabulary of injectable esters in a context where the underlying mechanism does not automatically apply.
The Practical Question
Independent analyses of products sold as RAD-150 have found ordinary RAD-140 inside.
That leaves two possibilities, neither good. Either the product is RAD-140 relabelled, in which case the buyer is paying a premium for nothing. Or it genuinely is the ester, in which case it delivers RAD-140 anyway once cleaved — with the same suppression, the same lipid damage, and the same liver risk that has produced published case reports of liver injury with RAD-140.
In both cases, what arrives is RAD-140. The ester adds cost and uncertainty rather than a benefit anyone has demonstrated.
Side Effects & Risks
- Everything associated with RAD-140: strong suppression, severe HDL suppression, elevated liver values
- Documented case reports of drug-induced liver injury with the parent compound
- Complete absence of characterisation data for the ester itself
- High likelihood that the product is not what the label says
- No manufacturing oversight
Blood Work & Monitoring
- Liver values (ALT, AST, GGT, bilirubin) — RAD-140 has case reports of liver injury; this is the priority
- Total and free testosterone, LH, FSH — before, during and after
- Lipid profile (LDL, HDL, ApoB)
- Estradiol (sensitive assay)
Legal status by region
Regulation differs considerably between jurisdictions and changes over time. This is a rough orientation, not legal advice — check the rules that apply where you are.
| Region | Regulatory status |
|---|---|
| United States | Not approved; FDA warning applies to the SARM category |
| EU / UK | No marketing authorisation |
| Most other jurisdictions | Unregulated grey area |
| Competitive sport | Prohibited at all timesAs a claimed RAD-140 derivative it falls under WADA S1.2, and it would metabolise to a detectable parent compound. |