spec sheet11 rows
RAD-150 (TLB-150 Benzoate) is a research chemical marketed as an ester form of the popular SARM RAD-140 (Testolone), promoted for building muscle and strength with a potentially longer-acting profile [1]. Like other selective androgen receptor modulators, it is intended to stimulate the androgen receptor in muscle and bone, but RAD-150 itself has no published pharmacological or clinical studies, so its profile is inferred from RAD-140 and the broader SARM class [1]. It is an unapproved, WADA-banned research chemical, and the RAD-140 family it is based on has been linked in case reports to serious cardiovascular harm [1][2][3].
- Built on RAD-140, a muscle builder in animals
- Ester design for steadier, longer-lasting levels
- High androgen receptor affinity and selectivity
- Orally active by design
- Strength and lean mass are the target
- As a SARM it is expected to suppress the body's natural testosterone production
Overview
RAD-150, also sold under the name TLB-150 Benzoate, is a research chemical marketed as a benzoate ester of RAD-140 (Testolone), one of the better-known selective androgen receptor modulators (SARMs) [1]. In vendor descriptions the addition of a benzoate ester group is presented as analogous to the esterification of testosterone, a modification intended to slow release and extend the compound's duration of action; it is important to note that this rationale comes from marketing and chemical analogy rather than from published pharmacokinetic studies of RAD-150 itself [1].
SARMs are a class of compounds that bind the androgen receptor, the same receptor activated by testosterone, and were designed to promote anabolic effects in muscle and bone while limiting androgenic effects elsewhere; despite substantial pharmaceutical research into indications such as muscle wasting and cachexia, no SARM has received full clinical approval [1]. RAD-150 is a newer entrant to this market and, unlike its parent RAD-140, has essentially no dedicated scientific literature: it has not been characterized in published human or animal studies, and any account of its effects is extrapolated from RAD-140 and the SARM class rather than from direct evidence [1].
RAD-150 is not approved by the United States Food and Drug Administration or any comparable regulator, and as a SARM-class agent it falls under the World Anti-Doping Agency Prohibited List, making it banned in competitive sport [1]. It is sold as a research chemical, typically as a liquid solution or capsules, in a market where analytical studies have repeatedly found SARM products to be mislabeled or to contain undisclosed ingredients [7]. Given that the closely related RAD-140 has been the subject of medical case reports describing serious adverse events, the absence of safety data specific to RAD-150 is a significant concern rather than a reassurance [2][3][4].
- RAD-150 has no published pharmacological or clinical studies of its own; everything claimed about it is inferred from the related compound RAD-140.
- The name TLB-150 Benzoate reflects its promotion as an ester, by analogy to testosterone esters that release their active molecule slowly, though this longer-acting behavior has never been confirmed in any study.
- Like its parent RAD-140, it is prohibited in sport by the World Anti-Doping Agency.
Mechanism
Because RAD-150 (TLB-150 Benzoate) has not been studied in published pharmacology, its presumed mechanism is understood through its parent compound RAD-140 and the selective modulator (SARM) class. SARMs act on the androgen receptor, the intracellular receptor through which testosterone and dihydrotestosterone stimulate muscle protein synthesis and growth [1]. They were engineered to activate this receptor preferentially in muscle and bone, aiming to produce anabolic, muscle-building effects with fewer of the androgenic effects that testosterone exerts on tissues such as the prostate [1]. RAD-140, the compound RAD-150 is derived from, is a potent nonsteroidal , and RAD-150 is presented as its benzoate ester, a form that by analogy to testosterone esters would be expected to release the active molecule more gradually; this expectation, however, has not been confirmed in any published study of RAD-150 [1].
The intended benefit of such a compound, increased muscle mass and strength, has not been demonstrated for RAD-150 and is only weakly supported even for the parent. In a long-term study in mice, RAD-140 given at 5 mg/kg failed to improve muscle strength and instead increased frailty and mortality risk, indicating that potent androgen-receptor stimulation of this kind does not necessarily translate into a clean anabolic gain [5]. No human clinical trials support safe, effective muscle building with RAD-140, and there are none at all for RAD-150 [1].
The safety considerations that dominate the RAD-140 family apply directly to RAD-150 by association. Androgen receptors are present in cardiac and vascular tissue, and RAD-140 has been linked in medical case reports to serious cardiovascular events in young users, including acute myocarditis, myopericarditis, and fatal heart failure, as well as to severe events such as spontaneous splenic rupture when combined with other performance-enhancing agents [2][3][4][6]. Because RAD-150 is chemically close to RAD-140 but even less studied, and because SARM products are frequently mislabeled, its true potency, pharmacokinetics, and safety in humans remain entirely uncharacterized, and the documented harms of its parent compound should be regarded as the most relevant available guide [5][6][7].
receptor fingerprint
Selective high-affinity agonist (via RAD-140)
Skeletal muscleAnabolic stimulation
AR/ER positive breast cancer cellsAR agonism with ESR1 repression
Safetyrisks and cautions, not medical advice
RAD-150 (TLB-150) is an unapproved research SARM, a benzoate ester of RAD-140, with no data supporting human use and no status as a licensed medicine. Like other androgen receptor agonists it is expected to suppress the hypothalamic-pituitary-testicular axis and lower natural testosterone, reduce HDL cholesterol, and strain the liver, and drug-induced liver injury has been reported with RAD-140. Its long-term and cardiovascular safety in humans are unknown.
History
RAD-150, marketed as TLB-150 Benzoate, is a research chemical presented as a benzoate ester of the selective androgen receptor modulator RAD-140 (Testolone). RAD-140 itself was developed by the biopharmaceutical company Radius Health and first described in the scientific literature around 2011 as a nonsteroidal androgen receptor agonist for muscle wasting and other indications. RAD-150 emerged later within the supplement and research-chemical trade, promoted on the analogy of testosterone esters, which release their active molecule gradually, as a longer-acting version of RAD-140.
Crucially, this claim has never been tested: RAD-150 has no published pharmacological or clinical studies of its own, and everything inferred about it is extrapolated from its parent compound and the broader SARM class. It has never been an approved drug, was not created through any formal clinical development program, and is banned in sport by the World Anti-Doping Agency. As such it has essentially no documented scientific history beyond that of RAD-140.
Reputation
RAD-150 is marketed to bodybuilders as an improved, longer-acting cousin of the popular RAD-140, and it carries some of that reputation for driving muscle and strength gains by association. It is important to be candid that this reputation is almost entirely borrowed: because no published study has ever characterized RAD-150's potency, pharmacokinetics, or safety in humans or animals, its supposed advantages remain unverified marketing claims.
The evidence that does exist concerns its parent, RAD-140, and it is cautionary; RAD-140 has been linked in case reports to serious liver injury and cardiovascular harm in young users, and a rodent study found it worsened frailty and survival. Given that RAD-150 is chemically close to RAD-140 but even less studied, and that SARM products are frequently mislabeled, the honest assessment is that its benefits are speculative while the documented risks of its parent compound should be treated as the most relevant guide.
Subjective profileweighing the evidence above
Not recommended. There is no published pharmacology on the molecule itself, so it is sold entirely on the reputation of RAD-140, which has reported cases of drug-induced liver injury of its own. Expect suppressed natural testosterone and falling HDL, with no approved use and no way to verify what is in the bottle.
Where to buy
Suppliers
Vendors carrying RAD-150, with live product details and codes. Links are affiliate links that support the wiki at no cost to you.
Kimera Chems
RAD-150
Research
- 2018first citedDetection of SARMs in doping control analysis.
- 2026most recentSpontaneous Splenic Rupture in a Patient With Recent Use of Performance-Enhancing Compounds: A…
- 1.Detection of SARMs in doping control analysis.
- 2.Selective androgen receptor modulator abuse-induced heart failure: catastrophic effects of RAD-140 (Testolone).
- 3.Acute Myocarditis From the Use of Selective Androgen Receptor Modulator (SARM) RAD-140 (Testolone).
- 4.Myopericarditis Following Use of Selective Androgen Receptor Modifier "RAD-140".
- 5.RAD140 (Testolone) negatively impacts skeletal muscle adaptation, frailty status and mortality risk in female mice.
- 6.Spontaneous Splenic Rupture in a Patient With Recent Use of Performance-Enhancing Compounds: A Case Report and Literature Review.
- 7.Development and validation of liquid chromatography-tandem mass spectrometry method for screening six selective androgen receptor modulators in dietary supplements.
- 8.RAD-140 Drug-Induced Liver Injury
8 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
Is RAD-150 the same as RAD-140?
It is a benzoate ester of RAD-140. The ester is meant to extend the half-life, but it has no research of its own.
Is there human data?
Not for RAD-150. RAD-140 reached an early human trial in breast cancer, but the ester form is entirely unstudied.
Will it suppress testosterone?
Almost certainly, given the androgenic mechanism; a longer-acting ester could make suppression more prolonged.
Limitations of the evidence
- RAD-150 has no published human or animal safety data of its own
Adverse effects
- As a SARM it is expected to suppress the body's natural testosterone production
Notes and cautions
- Its closely related parent RAD-140 has been linked in case reports to serious heart problems in young users
- It is an unapproved research chemical, and SARM products are frequently mislabeled or contaminated
- It is banned in competitive sport and is not a legal dietary ingredient