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Trestolone 100 - Dragon Pharma Trestolone 100 - Dragon Pharma

Dragon Pharma

Trestolone 100 - Dragon Pharma

Injection · 100 mg/ml · 10 ml

In stock · ships within 24h Out of stock Ships from International · U.S Domestic
CompoundTrestolone Enanthate
Class19-nor injectable (research)
Half-lifeNot confirmed (ester)
DetectionNot confirmed (urine)
Liver toxicityNot confirmed (injectable)
Water retentionNot confirmed (estrogenic)
Almost every number a reader expects is missing here, and this note says why rather than filling the gap. Trestolone is 7alpha-methyl-19-nortestosterone, MENT, an experimental 19-nor androgen studied as a male contraceptive and never marketed; the published figure of about 40 minutes is the terminal half-life of the unesterified steroid after intravenous administration, and no half-life, detection window or hepatotoxicity profile for the enanthate appears in the sources used for this card. It is not 17-alpha-alkylated, it is not a substrate for 5alpha-reductase, it suppresses LH and FSH strongly, and it forms its own estrogenic metabolite, 7alpha-methylestradiol. The line also carries the acetate as Ment 50, a shorter-profile format.
Strength

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Trestolone 100 - Dragon Pharma
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Quality First

All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Buy Trestolone 100 by Dragon Pharma at Best Anabolic Steroids. One 10 ml multi-dose vial of trestolone enanthate at 100 mg per ml is the longer-ester half of a two-item line whose other half is the acetate sold as Ment 50. Trestolone was never marketed.

Trestolone is a controlled anabolic in most countries and a research chemical rather than a treatment for any condition.

Product Overview

The pack is a single vial: 10 ml of sterile injectable oil carrying 100 mg of trestolone enanthate per millilitre, or 1000 mg of ester in total, so the vial holds ten dose units. The closure is a multi-dose stopper, so the vial is entered repeatedly rather than opened once.

The active substance is 7alpha-methyl-19-nortestosterone, known almost everywhere as MENT. It is not a bodybuilding invention: it was built inside a male hormonal contraception programme, later examined as an androgen replacement candidate, and never brought to market. The skeleton is 19-nor, placing it beside nandrolone and trenbolone in the progestogenic part of the family, and it is one of the very few androgens with published human pharmacology, because that contraceptive work required real dosing studies in men.

The ester is a practical decision, not a marketing one. Published pharmacokinetic work measured a terminal half-life of roughly 40 minutes for the unesterified steroid after intravenous administration - far too short to hold a level - and an enanthate chain is the conventional answer to that. The sources behind this page do not give the resulting half-life of the enanthate, a detection window for its metabolites, or a hepatic profile.

Mechanism of Action

The enanthate chain does nothing on its own. Esterases in tissue and blood free the steroid over time, and the liberated molecule binds the androgen receptor and drives what any androgen drives: higher nitrogen retention, a faster rate of muscle protein synthesis and a stronger response to the same training load.

Trestolone is not a substrate for 5alpha-reductase. Testosterone's activity in scalp, skin and prostate is largely amplified by conversion to DHT, and that amplification does not happen to MENT, part of why it was researched as an androgen that would leave the prostate comparatively untouched. On the other side, its suppression of luteinising hormone and follicle-stimulating hormone is powerful even at low concentrations - the mechanism the contraceptive work exploited - and it stops spermatogenesis as a matter of course.

The estrogenic pathway is what readers most often get wrong. Trestolone aromatises into 7alpha-methylestradiol, an estrogenic metabolite in its own right, so a 19-nor label does not mean the compound is estrogen-free. A routine estradiol assay therefore does not simply read its estrogenic activity off the report, and any aromatase inhibitor decision has to rest on symptoms and on real laboratory numbers.

What to Expect While Trestolone Is Running

  • Timing follows the ester, and nobody has measured it. The acetate in Ment 50 appears and clears faster and the enanthate here is the slower profile, but no published timeline exists for either format.
  • A stronger anabolic drive is the expectation, not a documented result, because it follows from the compound's mechanism and its 19-nor relatives rather than from published human data.
  • Natural hormone production stops. LH, FSH and spermatogenesis fall hard, so the exit is planned before the first injection, not after the last one.
  • Estrogen symptoms can appear even though this is not testosterone, because the metabolite is 7alpha-methylestradiol; water retention and nipple sensitivity are possible rather than impossible.
  • The unknowns stay unknown. No human data set describes lipids, blood pressure, acne or hepatic markers on trestolone as an anabolic, so bloodwork is the only substitute for the missing profile.

Dose, Strength and the Choice Between Trestolone 100 and Ment 50

There is no honest dosing table for trestolone. What the literature holds are contraceptive and replacement protocols that do not translate into a bodybuilding course.

Beginner Not confirmed; no published human dose for trestolone as an anabolic exists in the sources used here
Intermediate Not confirmed; the compound circulates outside medicine, but there are no peer-reviewed dose levels to cite
Advanced Not confirmed; a milligram figure here would be invention, not documentation
Female Not confirmed; no data exist, and a 19-nor with progestogenic activity plus heavy gonadotropin suppression is not treated as a female option
Administration Intramuscular injection of the ester with a fresh needle each time; the injection frequency for the enanthate is not fixed in the sources used here
Strength and format 100 mg per ml in 10 ml in this vial, against 50 mg per ml in 10 ml for the acetate, so the choice is about how quickly the level builds and clears, not about potency

The comparison worth keeping in view is the other 19-nors: Deca 300 and Trenbolone 100 are the family members whose behaviour is actually documented, and trestolone shares their suppression of the gonadal axis without being either of them.

Combining Trestolone 100 with Other Compounds

Any combination involving this compound is non-medical practice rather than a research finding, and the cards below are labelled that way. What they document is the logic readers apply.

One compound, two ester profiles
Trestolone 100 - enanthate, slower release + Ment 50 - acetate, quicker release
Non-medical practice; the acetate is chosen when a faster exit is wanted, not when a better result is expected
19-nor logic with a conventional base
Trestolone 100 - dose not established + Enantat 250 - androgen base + HCG 5000 iu - support during the run
Non-medical practice; borrowed from the 19-nor class, where the axis stops completely and a base plus a planned exit is the usual answer
Recovery built around the run
Trestolone 100 - duration unconfirmed + Nolvadex - post-cycle therapy + Clomid - alternative SERM route
Recovery planning rather than a course: LH and FSH suppression is profound here, so the exit is designed before the entry

Because the suppression is heavy, the products that matter most in a trestolone plan are the ones that control estrogen and restart the axis - Aromasin when a laboratory result or clear symptoms justify it, and a SERM afterwards.

Recovery Planning After Trestolone

The suppression this compound produces is strong enough that recovery is the defining phase of any run, and the timing is one more thing the sources do not pin down. The scheme below is the recovery pattern used across this catalogue, applied to a compound with no recovery study of its own.

OnsetNot fixed in the sources used for this card; LH, FSH and testosterone results decide the start rather than a calendar
Option ANolvadex 40 mg per day for 2 weeks, then 20 mg per day, following the standard reference scheme for this site
Option BClomid 50 mg per day, using the standard reference scheme
Length4-6 weeks is the scheme used across this catalogue; there is no trestolone-specific recovery study to refine it
Follow-upTotal testosterone, LH, FSH, estradiol and prolactin, with the prolactin line managed by a dopamine agonist under laboratory control

One detail is specific here: because the enanthate half-life is undocumented, the wait between the last injection and the start of therapy cannot be calculated from a table and has to be judged from the laboratory picture.

Trestolone Side Effects and Precautions

Half of the usual grid is blank here, not because the risks are small but because nobody published the data.

Suppression of LH, FSH and spermatogenesisPost-cycle therapy with a SERM plus laboratory checks of LH, FSH and testosterone. A class effect, pronounced even at low concentrations.
Prolactin line (19-nor, progestogenic)A dopamine agonist such as cabergoline, but only where a test confirms hyperprolactinemia; there are no MENT-specific data on this pathway.
Estrogenic effects from 7alpha-methylestradiolEstradiol monitoring and an aromatase inhibitor only by indication, for example Aromasin; the metabolite is described in the literature, clinical data are not.
Lipids, blood pressure and acneNot confirmed - no human data set exists for the anabolic use of MENT; bloodwork before and during the run is the only substitute.
Cardiovascular and hepatic questionsNot confirmed - not being 17-alpha-alkylated is not the same as being characterised. Baseline and follow-up labs.
Injection-site reactionsFresh needle and swab each time, rotate sites, and stop if a site becomes hot, swollen or painful rather than treating it as routine soreness.

Storing Trestolone 100 Before and During Use

Keep the vial in its carton, upright, away from light and out of reach of children, at ordinary room temperature rather than in a refrigerator or freezer: cold storage is not required for an oil-based ester, and temperature swings are more likely to push the compound out of solution than to protect it. Wipe the stopper with an alcohol swab and let it dry before every needle goes in, never reuse a needle, and note the first-entry date on the label so the age of an opened multi-dose vial stays visible.

Buying Trestolone 100 Online

Because this is a compound where most of the internet is fiction, and this page is built the other way round. The vial is Dragon Pharma trestolone enanthate at 100 mg per ml in 10 ml. It ships with lab-tested packaging under the site's international and US delivery terms, and every unconfirmed value on this page stays visibly unconfirmed rather than borrowing a number from nandrolone. If you want a straight account of what trestolone is, what the research measured and how an exit is planned around its suppression, this is it.

The information on this page is reference material for research and educational purposes and is not medical advice, a prescription or a treatment recommendation. Trestolone is described here as an injectable research chemical and an experimental substance that was never approved for human use; it is not presented as a medicine for any condition. The text deliberately leaves unconfirmed values unstated instead of estimating them. Amounts, timings and laboratory figures quoted elsewhere in this catalogue do not transfer to this compound automatically. Handle as a laboratory item, keep it away from children, and follow the law where you live.
What is Trestolone (MENT)?
It is 7alpha-methyl-19-nortestosterone, an experimental injectable androgen and progestogen developed in a male contraception programme and never marketed. Dragon Pharma supplies it as Trestolone 100, an enanthate at 100 mg per ml, and as Ment 50, an acetate at 50 mg per ml.
Is trestolone a steroid or something else?
It is an anabolic steroid by structure and action - a 19-nor androgen - but it also carries progestogenic activity, which is part of why it was studied as a contraceptive. It sits on the WADA prohibited list within the anabolic agents class, and it is not a dietary supplement, a peptide or a research chem in the usual lab-reagent sense.
Does trestolone aromatize?
It has its own estrogenic route: the metabolite 7alpha-methylestradiol is described in the literature, so the compound produces estrogenic activity rather than being free of it. What is missing is clinical data on how much of that activity a user actually sees. That is the difference between a described metabolite and a documented side effect profile.
Trestolone dosage - are there published human doses?
Not for anabolic use. The research that exists examined it as a contraceptive and as a candidate for androgen replacement, under protocols that were not designed as bodybuilding cycles. The sources used for this page record no beginner, intermediate or advanced dose, and no cycle length, which is why the dosage table above says not confirmed on every line.
Why is MENT used as a male contraceptive?
Because it suppresses gonadotropin release powerfully even at low concentrations, which stops spermatogenesis. In contraceptive research that effect is the point. In any other context the same mechanism is the main liability, since it means LH and FSH shut down and recovery depends on a planned post-cycle therapy rather than on time alone.
What is the difference between Ment 50 and Trestolone 100?
The ester and the concentration. Ment 50 is the acetate at 50 mg per ml, chosen for a shorter profile, and Trestolone 100 is the enanthate at 100 mg per ml, the longer of the two. Because the unesterified steroid is cleared in roughly 40 minutes after intravenous administration in published data, the ester is what makes a practical injection interval possible - though the exact interval for the enanthate is not stated in the sources used here.
Do I need to taper or run a PCT with Trestolone?
Tapering is not part of the reference material - the ester clearance does that by itself. Post-cycle therapy is a different matter: with gonadotropins suppressed that deeply, recovery is planned in advance. The catalogue scheme is Nolvadex or Clomid for 4-6 weeks, with LH, FSH, testosterone, estradiol and prolactin checked afterwards; no trestolone-specific recovery study exists to narrow that down.
Is trestolone approved for human use?
No. It was developed in a contraceptive programme and studied as a replacement-therapy candidate, and it never reached the market. That is the origin of every gap in this page: without a marketed drug there is no label, no approved dose, no defined detection window and no human side effect profile to quote.

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