RAD 150
1049.99 $
Super concentrated formula
50
RAD150
**These statements have not been evaluated by the Food and Drug
administration (FDA). This product is not intended to diagnose, treat,
cure, or prevent any disease.
*All amounts per 1Ml serving
RAD 150 formulation
RAD 150, also known as TLB 150, is the esterified version of the popular SARM, RAD 140. RAD 140 has been studied most thoroughly on male gonadectomized rats suffering from neurodegenerative decline due to decreased androgen levels. Overall, the fascinating study conducted by Jayaramen et. Al came to the conclusion that in male rats, supplementation with RAD 140 had neuroprotective effects on the brain via MAPK signaling. Additionally, the study found that treatment with RAD 140 was actually just as effective in protecting against cell death as testosterone treatment Study.. In addition to providing neuroprotection, testing of RAD 140 in juvenile monkeys over a 28 day period was shown to have led to an average of 10% increase in body weight. Through the use of DEXA scans it was found that the weight gain was primarily lean muscle mass.
Esterification occurs when a substitution reaction takes place. The specific substitution reaction that occurs when a compound becomes an ester, is derived from a carboxylic acid. The hydroxyl group (-OH) of the carboxylic acid is replaced with an alkyl (-O-) group. Esterification occurs when the carboxylic acid is exposed to heat and a strong acid, normally sulphuric acid. In some cases, various other strong acids such as hydrochloric acid will be used in order to catalyze the substitution reaction Study..
RAD 150 is the esterified version of RAD 140. The main structural difference between the two compounds is the group of benzoate esters that were added during the substitution reaction of esterification. Adding the group of benzoate esters increases the alkalinity of the compound thus making it more stable than RAD 140 itself Study.. In order to synthesize RAD 150 from Testolone, it has to undergo the process of esterification. During the substitution reaction, a group of benzoate esters is added to Testolone in order to turn the compound into its esterified version, accounting for the main structural difference between the two compounds. By adding the benzoate ester group, the compound now has increased alkalinity, thus indicating that the esterified compound is more stable than Testolone Study. Additionally, in a similar fashion to other esterified SARMs, the bioavailability and the half-life of RAD 150 are increased. With increased bioavailability, the compound is absorbed much faster, and with increased half-life the compound is active for far longer than RAD 140, the nonesterified compound. This indicates that by esterifying RAD 140 there are additional potential benefits that are added. Furthermore, when comparing Testolone to RAD 150, RAD 150 is similar to other esterified SARMs with an increase in half-life and bioavailability. By increasing the half-life of RAD 150, the compound is considered active for a longer period of time than when supplementation with Testolone. Additionally, when bioavailability is increased, the compound is absorbed at a faster rate. It can be concluded that when Testolone undergoes esterification, there are several additional benefits that can be derived from the resulting compound, RAD 150.
possible side effects
Not for human consumption, Please read the research papers related to this chemical before administration, Misuse of this product can result in dangerous side effects.