Trestolone MENT Transdermal (Liquid) – Product Details

Trestolone Acetate, also known as MENT, is a synthetic androgen initially developed for its potential as a male contraceptive and potential androgen replacement in testosterone-deficient men. [R]

Trestolone is being researched as a potential inhibitor of releasing the luteinizing hormone (LH) and follicle-stimulating hormone (FSH). A process called spermatogenesis, the process where new sperm is produced, requires both testosterone and FSH. This may be impaired by the reduction in FSH potentially caused by trestolone, the reduction in LH, and the subsequent reduction in testosterone.

• This Transdermal Liquid is offered at 17mg per ml/60ml/1g.
• CAS Number is stated as 6157-87-5\
• Molar Mass is 330.468 g·mol−1
• It has a Chemical Formula of C21H30O3
• IUPAC Name: 7α-methyl-19-nortestosterone
• Also known by Synonyms as Trestolone acetate

What is Trestolone Acetate (MENT) Transdermal?

Trestolone acetate, also known as 7-methyl-19-nortestosterone (MENT) or trestolone acetate, is an experimental androgen medication being researched as a form of hormonal birth control for men. [R]

It comes in an injectable form with a chemical formula of C21H30O3.

Trestolone acetate, whose function resembles a synthetic steroid, limits sperm production in men suppressing a process called spermatogenesis, but it does not affect a man’s sexual functionality. [R]

For this very reason, the compound is considered an effective male contraceptive, similar to the S-23 SARM, although more research is required to confirm this.

MENT has a very high affinity for the AR receptor. According to research, it is far greater than testosterone. However, it has a high ability to aromatize.

Trestolone’s effects on testosterone are opposite to that of testosterone enanthate since the latter is used to increase testosterone levels.

MENT trestolone acetate is an experimental drug that is inadvisable for human consumption, although it could function as a potent anabolic steroid.

One should recognize trestolone acetate side effects which is an essential factor in using this potential inhibitor of testosterone production.

Possible Uses of Trestolone Acetate

MENT, also known as trestolone acetate, is a potentially highly potent androgen receptor agonist currently being researched.

According to reliable laboratory test results, a single research cycle can achieve beneficial outcomes such as muscle growth in weeks.

Here are the desirable expected outcomes of MENT trestolone acetate for its users according to laboratory tests:

Trestolone Acetate MENT May Help Lose Body Fat

It was discovered in recent research on hypogonadal rats that trestolone acetate MENT decreased endocortical bone growth and bone turnover rate more significantly than testosterone, as well as fat mass and serum leptin. [R]

Trestolone Acetate MENT May Help in Achieving Lean Body Physique

Those who try to improve their physique through persistent and systematic training will understand the various methods for achieving their workout objectives. Trestolone acetate is one such method for possibly achieving a slim, toned body while also increasing muscle mass.

The more strong androgen MENT was demonstrated to be beneficial in correcting adverse alterations in bone and muscle tissue in a preclinical animal model of male hypogonadism, even when delivered at a later stage. [R]

Trestolone Acetate MENT May Be Used in Male Birth Control Therapy

A large human study on male subjects compared the effects of MENT to testosterone, both with the progestin etonogestrel, on spermatogenesis and sex drive and safety biomarkers associated with androgen use. This was a rigorous study with 29 subjects tested for 48 weeks. [R]

Compared to testosterone, this study shows that MENT is possibly a safer and more effective form of male medical birth control. The study’s main finding is that MENT appears to be relatively safe on lipids and other biomarkers, but it does require post-cycle therapy to restore LH and FSH levels to normal. [R]

MENT reduced luteinizing hormone more strongly than testosterone, which may be of therapeutic interest in its possible use as a male contraceptive. [R]

How Does Trestolone Acetate Work

Trestolone works by inducing temporary infertility by reducing pituitary gonadotropin release.

The steroid also suppresses the production of gonadotropins, follicle-stimulating hormone, and luteinizing hormone, even in small quantities. The follicle-stimulating hormone (FSH) and luteinizing hormone (LH) are essential for spermatogenesis, the process by which the testes make spermatozoa.

MENT has a higher metabolic clearance rate than testosterone and, unlike testosterone, does not bind to the sex hormone-binding globulin (SHBG).

Spermatogenesis is prevented when the release of LH and FSH is suppressed. Suppressing LH further reduced sperm production and decreased testosterone production, resulting in infertility. MENT powder is an appropriate replacement medication for the majority of androgen-dependent tasks.

Safety and Side Effects

People who research trestolone acetate should be aware of the adverse effects it can have on test subjects.

Again, the lack of long-term studies and clinical research on MENT trestolone acetate makes it challenging to understand the side effects in a clinical setting.

Having said that, the side effects are very similar to those experienced when running low-dose testosterone and trenbolone steroid cycle.

Some of the possible side effects of trestolone acetate:

• Insomnia
• Upset Stomach
• Heart Burn
• Back Acne
• Night Sweats
• Diarrhea

If your test subjects note any of these, it is advisable to cease administration immediately. We still do not know how common these side effects are.

Frequently Asked Questions

What Does Testosterone Do?

Testosterone is a sex hormone that has numerous functions in the body.

It is believed to regulate libido, bone mass, fat distribution, muscle mass, strength, and the production of red blood cells and sperm in men.

What is a Follicle Stimulating Hormone?

The pituitary gland in the brain produces follicle-stimulating hormone (FSH).

The follicle-stimulating hormone is essential for the normal functioning of men’s and women’s reproductive systems.

In men, follicle-stimulating hormone stimulates sperm production by acting on the Sertoli cells of the testes (spermatogenesis).

Does the use of MENT require an aromatase inhibitor?

MENT oral and transdermal doses may be somewhat more effective than injectable dosing. To treat the study subjects’ prolactin and estrogen-related adverse effects, an aromatase inhibitor such as Arimidex and a prolactin inhibitor such as Cabergoline should be at hand.

Does MENT have the potential to treat prostate cancer?

The capacity of 7 alpha-methyl-19-nortestosterone acetate (MENT) to enhance the weights of castrated rats’ ventral prostate and seminal vesicles was four times that of testosterone. This is also why it is less likely to promote prostate enlargement, and it may even be advised for the treatment of particular prostate disorders such as prostate cancer.

However, this application is still not proven and requires more human clinical studies. muscle wasting

Why Buy Trestolone Acetate (MENT) from Behemoth Labz

Behemoth Labz is a safe place to buy trestolone acetate online. We provide accurate product details and high-quality research chemicals to ensure you get your money’s worth.

Summary

Synthetic androgen 7-methyl-19-nortestosterone (MENT) is a potential androgen replacement therapy for male hypogonadism. MENT is a more potent androgen than Testosterone, with a lower dose sufficient for the restoration of androgen-sensitive organs in rats.

Furthermore, because MENT suppresses gonadotrophins, it has the potential to be used in male contraception as well as male hypogonadism.

When administered immediately after castration at relatively low doses without overstimulation of the prostate, MENT does indeed prevent bone and muscle loss.

MENT, despite restoring sexual function, failed to maintain lumbar spine bone density in hypogonadal men in this small single-center trial.

These findings highlight the need for additional preclinical testing of this compound’s effects on non-reproductive tissues.

Variation	60ml / 17mg per ml / 1g