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DHB Dihydroboldenone Cypionate - Xeno Laboratories

Xeno Laboratories

DHB Dihydroboldenone Cypionate - Xeno Laboratories

Injection · 200 mg/ml · 10 ml

Out of stock
CompoundDihydroboldenone Cypionate
ClassInjectable androgen
Half-lifeVendor says 6 days
DetectionNot confirmed
Liver toxicityLow
Water retentionNone
An oily solution of 1-testosterone with a cypionate ester, and the one injectable in this line that is famous for the wrong reason: a large share of users find the shots markedly painful. The compound does not aromatise, so the tissue built is dry and hard, and the strength and density arrive gradually across two to four weeks.
DHB Dihydroboldenone Cypionate - Xeno Laboratories
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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.

DHB is Xeno Laboratories' dihydroboldenone cypionate, an oily solution for deep intramuscular injection. The shorthand DHB, or 1-testosterone, is more common than the full name, and the compound sits in the DHT branch of the family where nothing can be converted to estrogen.

Its reputation rests on two things that pull in opposite directions. The tissue it builds is dry and dense, which is what attracts users, and the injections are notably uncomfortable for a large share of them, which is what limits the amount people are willing to run.

Product Overview

Dihydroboldenone is 1-testosterone, a molecule that is a DHT derivative with a double bond in the first ring. The practical effect of that structure is a strong androgen that cannot aromatise at all, so fluid retention and chest tissue are not expected results of using it. The cypionate ester attached to it is a longer chain, described in the project reference material as an ester requiring two or three injections a week, while some vendor pages quote a figure of roughly six days for the half-life; that number has no independent confirmation, and it is presented here as a vendor statement rather than an established value.

Animal work is the only detailed pharmacology available. In those studies the substance matched testosterone propionate for growth of the prostate and the levator ani muscle at equal molar amounts, and it also increased liver weight, which is a laboratory finding rather than a documented human injury pattern. It is not a 17-alpha-alkylated compound, so the hepatic mechanism that makes oral methylated steroids risky does not apply in the same way.

Where it fits is a dry cycle. Testosterone usually supplies the base, and where a harder finish is wanted the compound is run beside an oral such as Winstrol or Anavar for a short block. The nearest dry injectable neighbour in this line is Primobolan 100, which builds more slowly and hurts far less.

Dosage Protocol

Amounts are set by tolerability as much as by pharmacology, because a dose that cannot be injected consistently is a dose that will not be run.

Beginner 200-300 mg a week for 8-10 weeks, starting at the bottom because of injection discomfort
Intermediate 300-400 mg a week for 10-12 weeks, split across two or three injections
Advanced 400-600 mg a week for 12 weeks; part of the range is simply not tolerated by many users
Female No confirmed data; the virilisation risk of a DHT-derived androgen is not something the sources treat as manageable
Administration Intramuscular, two or three times a week, rotating sites wide because of the injection reaction

The practical advice in the source material is about technique rather than numbers. Alternating sites across a wide area, using a smaller volume per injection and splitting the weekly total more finely all reduce the reaction, and that is the reason a lower concentration is often preferred even when it means more oil.

Suggested Protocols

Three arrangements cover the way it is used. Each pill opens the matching page in the Xeno line.

Dry mass block
A ten to twelve week block, with lipids and blood pressure checked as it runs
Recomposition with an oral finish
Twelve weeks, with the tablets concentrated at the end where the look matters most
Cutting without an oral
Fourteen weeks in a calorie deficit, without adding a methylated oral on top

What to Expect

  • Density rather than size. The look that emerges is hard and dry, with no subcutaneous fluid sitting over it.
  • Strength arrives over weeks two to four. The change is gradual, and the load on the bar moves before the tape measure does.
  • No chest tissue expected. A molecule that cannot aromatise has no route to gynecomastia from the compound itself.
  • Injection pain is the common complaint. A significant share of users report it, and for some it decides the ceiling on the amount they run.
  • Suppression starts early. Natural production falls within the opening weeks, so recovery has to be part of the plan from the start.
  • Blood pressure can drift. Readings tend to rise across a block, which is one of the values worth measuring at home.

Side Effects and Management

The two entries at the top of this list are what separates DHB from the other dry injectables.

Painful injectionsRotate sites widely, dilute to a lower concentration, keep the volume per shot small. Frequent and reported by a large share of users.
Falling HDL and rising LDLLipid panel during and after the block, dietary fat quality and aerobic work. Dose related.
Rising blood pressureHome readings, hydration and monitoring of hematocrit. Reported through a block at working amounts.
Oily skin and thinning scalp hairSkin and scalp care, with the weekly amount kept restrained. A DHT-derived androgen raises the odds in users who are predisposed.
Suppressed production and testicular sizeHCG during the cycle where a clinician advises it, and a SERM afterwards. Expected and reversible.
Masculinising effects in womenDo not use; stop immediately if anything appears. The risk applies at any amount.

Post-Cycle Therapy

The cypionate ester keeps releasing after the last shot, so therapy waits rather than starting straight away.

Starting pointTen to fourteen days after the final injection, while the ester finishes clearing
First routeTamox at 40 mg daily for a fortnight, then 20 mg daily for another two to four weeks
Second routeClomiphene at 50 mg daily for four to six weeks
Short blocksSuppression develops at any effective amount, so even an eight week run closes with a recovery protocol
BloodworkTotal and free testosterone, LH, FSH and estradiol, plus a lipid panel and liver enzymes, drawn four to six weeks after the therapy block closes
Offered as educational and laboratory reference material. Xeno DHB is a research-grade compound supplied for experimental work, not a medicine and not a treatment for any medical condition. Several figures quoted here, including the half-life, rest on vendor statements without independent confirmation, and the amounts reflect community and reference data rather than a clinical recommendation. Nothing here is medical advice. Keep the product away from children and respect local regulations.
What is DHB?
DHB is the shorthand for dihydroboldenone, also called 1-testosterone. It is an injectable androgen built on a DHT backbone with a cypionate ester, and it cannot convert to estrogen, which is what gives it the dry, dense reputation it carries.
What amount is normally run each week?
Community and vendor figures cluster in the low hundreds of milligrams a week, with 200 to 300 mg as a starting range for eight to ten weeks, 300 to 400 mg for ten to twelve weeks, and the upper end of the range near 400 to 600 mg. Tolerability rather than pharmacology usually sets the ceiling, because the injections are painful for many users.
Does DHB aromatize?
No. There is no route from this molecule to estradiol, so fluid retention and gynecomastia are not expected effects of the compound. That does not make the cycle gentle, because blood pressure, lipids and the body's own testosterone production all move anyway.
Why does DHB hurt so much to inject?
The reaction is well documented in user reports and the project fact base records it as a known characteristic of the compound rather than a fault in one batch. The usual mitigations are a lower concentration, a smaller volume per injection and wide site rotation; none of them removes it entirely, and it is the most common reason people abandon a DHB block.
What is the half-life of DHB?
No independently confirmed figure exists. The project reference material treats it as a long ester needing two or three injections a week, while some vendor pages quote roughly six days; that number is repeated here as a vendor statement only. Schedules are therefore built around two or three weekly injections rather than around a precise number.
Is DHB hard on the liver?
It is not 17-alpha-alkylated and it is injected, so the mechanism behind the hepatic risk of methylated orals does not apply. Animal studies did record an increase in liver weight, which is a laboratory observation rather than a documented pattern of injury in humans; enzymes are still worth including in the routine bloodwork.
How long does DHB stay detectable?
Detection is by gas chromatography and mass spectrometry, looking for 1-testosterone and its metabolites, and the substance sits in the WADA class S1 group of anabolic agents. An exact clearance window is not confirmed in the sources used for this page, so no figure is offered rather than a guess.
Is post-cycle therapy needed afterwards?
Yes. The compound shuts down the body's own testosterone, so a recovery protocol follows the block. Because the cypionate ester is still releasing, the first dose waits ten to fourteen days after the closing injection, and the repeat panel, lipids and liver enzymes included, is drawn four to six weeks after that protocol finishes.

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