Oral Turinabol (chlorodehydromethyltestosterone) anabolic steroid profile and dosage

akn · May 30, 2014

<!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves/> <w:TrackFormatting/> <w

unctuationKerning/> <w:ValidateAgainstSchemas/> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w

oNotPromoteQF/> <w:LidThemeOther>EN-US</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables/> <w:SnapToGridInCell/> <w:WrapTextWithPunct/> <w:UseAsianBreakRules/> <w

ontGrowAutofit/> <w:SplitPgBreakAndParaMark/> <w

ontVertAlignCellWithSp/> <w

ontBreakConstrainedForcedTables/> <w

ontVertAlignInTxbx/> <w:Word11KerningPairs/> <w:CachedColBalance/> <w:UseFELayout/> </w:Compatibility> <w

oNotOptimizeForBrowser/> <m:mathPr> <m:mathFont m:val="Cambria Math"/> <m:brkBin m:val="before"/> <m:brkBinSub m:val="--"/> <m:smallFrac m:val="off"/> <m:dispDef/> <m:lMargin m:val="0"/> <m:rMargin m:val="0"/> <m:defJc m:val="centerGroup"/> <m:wrapIndent m:val="1440"/> <m:intLim m:val="subSup"/> <m:naryLim m:val="undOvr"/> </m:mathPr></w:WordDocument> </xml><![endif]--> Description:
Chlorodehydromethyltestosterone is a potent derivative of
Dianabol. This oral steroid is structurally a cross between
methandrostenolone and clostebol (4-chlorotestosterone),
having the same base structure as Dianabol with the added 4-
chloro alteration of clostebol. This alteration makes
chlorodehydromethyltestosterone a milder cousin of
Dianabol, the new steroid displaying no estrogenic and a
much less androgenic activity in comparison to its more
famous counterpart. The anabolic activity of
chlorodehydromethyltestosterone is somewhat lower than
that of Dianabol as well, but it does maintain a much more
favorable balance of anabolic to androgenic effect. This
means that at any given level of muscle-building activity,
chlorodehydromethyltestosterone will be less likely to
produce androgenic side effects.
History:
Chlorodehydromethyltestosterone was first described in
1962.564 Jenapharm (Jena, Germany) soon after released the
drug for sale in the East German prescription drug market,
under the brand name Oral Turinabol. The drug was favored
by clinicians for its highly anabolic and low anabolic nature,
lending itself to use in not only adult males, but women and
children as well. The product was manufactured in two
strengths, containing 1 mg and 5 mg of drug per tablet, so that
a lower-dosed version was available for the more sensitive
populations. Chlorodehydromethyltestosterone was applied
for a number of medical uses; mainly those focusing on the
building or preservation of lean muscle tissue and bone
mass.
Oral Turinabol became a steroid of infamy during the
1990’s, when it was revealed that
chlorodehydromethyltestosterone had been one of the closely
held secrets inside the “East German Doping Machine.” This
steroid products as well). Before or since, no other brand of
chlorodehydromethyltestosterone has existed as a
prescription drug product. Today, this agent is still available,
but is only produced by a small number of underground
manufacturers and export-only suppliers.
How Supplied:
Chlorodehydromethyltestosterone is not available as a
prescription drug product. When manufactured, it was found
in 1 mg and 5 mg tablets, sold in Germany/German
Democratic Republic.
Structural Characteristics:
Chlorodehydromethyltestosterone is a modified form of
testosterone. It differs by: 1) the addition of a methyl group at
carbon 17-alpha, which helps protect the hormone during
oral administration, 2) the introduction of a double bond
between carbons 1 and 2 (1-ene), which shifts the anabolic
to androgenic ratio in favor of the former, and 3) the
attachment of a chloro group at carbon 4, which inhibits
steroid aromatization and reduces relative androgenicity.
Side Effects (Estrogenic):
Chlorodehydromethyltestosterone is not aromatized by the
not necessary when using this steroid, as gynecomastia
should not be a concern even among sensitive individuals.
Since estrogen is the usual culprit with water retention, this
steroid instead produces a lean, quality look to the physique
with no fear of excess subcutaneous fluid retention. This
makes it a favorable steroid to use during cutting cycles,
when water and fat retention are major concerns.
Side Effects (Androgenic):
Although chlorodehydromethyltestosterone is classified as an
anabolic steroid, androgenic side effects are still possible
with this substance. These may include bouts of oily skin,
acne, and body/facial hair growth. Doses higher than
normally prescribed are more likely to cause such side
effects. Anabolic/androgenic steroids may also aggravate
male pattern hair loss. Women are additionally warned of the
potential virilizing effects of anabolic/androgenic steroids.
These may include a deepening of the voice, menstrual
irregularities, changes in skin texture, facial hair growth, and
clitoral enlargement. Chlorodehydromethyltestosterone is not
extensively metabolized by the 5-alpha reductase enzyme, so
its relative androgenicity is not greatly altered by the
concurrent use of finasteride or dutasteride
Side Effects (Hepatotoxicity):
Chlorodehydromethyltestosterone is a c17-alpha alkylated
compound. This alteration protects the drug from
deactivation by the liver, allowing a very high percentage of
the drug entry into the bloodstream following oral
administration. C17-alpha alkylated anabolic/androgenic
steroids can be hepatotoxic. Prolonged or high exposure may
result in liver damage. In rare instances life-threatening
dysfunction may develop. It is advisable to visit a physician
periodically during each cycle to monitor liver function and
overall health. Intake of c17-alpha alkylated steroids is
commonly limited to 6-8 weeks, in an effort to avoid
escalating liver strain. The use of a liver detoxification
supplement such as Liver Stabil, Liv-52, or Essentiale Forte
is advised while taking any hepatotoxic anabolic/androgenic
steroids.
Side Effects (Cardiovascular):
Anabolic/androgenic steroids can have deleterious effects on
serum cholesterol. This includes a tendency to reduce HDL
(good) cholesterol values and increase LDL (bad)
cholesterol values, which may shift the HDL to LDL balance
in a direction that favors greater risk of arteriosclerosis. The
relative impact of an anabolic/androgenic steroid on serum
lipids is dependant on the dose, route of administration (oral
vs. injectable), type of steroid (aromatizable or non
aromatizable), and level of resistance to hepatic metabolism.
Chlorodehydromethyltestosterone has a strong effect on the
hepatic management of cholesterol due to its nonaromatizable
nature, structural resistance to liver breakdown,
and route of administration. Anabolic/androgenic steroids
may also adversely affect blood pressure and triglycerides,
reduce endothelial relaxation, and support left ventricular
hypertrophy, all potentially increasing the risk of
cardiovascular disease and myocardial infarction.
To help reduce cardiovascular strain it is advised to
maintain an active cardiovascular exercise program and
minimize the intake of saturated fats, cholesterol, and simple
carbohydrates at all times during active AAS administration.
Supplementing with fish oils (4 grams per day) and a natural
cholesterol/antioxidant formula such as Lipid Stabil or a
product with comparable ingredients is also recommended.
Side Effects (Testosterone Suppression):
All anabolic/androgenic steroids when taken in doses
sufficient to promote muscle gain are expected to suppress
endogenous testosterone production. Without the intervention
of testosterone-stimulating substances, testosterone levels
should return to normal within 1-4 months of drug secession.
Note that prolonged hypogonadotrophic hypogonadism can
develop secondary to steroid abuse, necessitating medical
intervention.
Administration (General):
Studies have shown that taking an oral anabolic steroid with
food may decrease its bioavailability.565 This is caused by
the fat-soluble nature of steroid hormones, which can allow
some of the drug to dissolve with undigested dietary fat,
reducing its absorption from the gastrointestinal tract. For
maximum utilization, this steroid should be taken on an empty
stomach.
Administration (Men):
A common clinical dose of chlorodehydromethyltestosterone
is estimated to be 5 mg per day; actual prescribing guidelines
are unavailable. In the athletic arena, an effective oral daily
dosage falls in the range of 15-40 mg, taken in cycles lasting
no more than 6-8 weeks to minimize hepatotoxicity. This
level is sufficient for measurable increases in lean muscle
mass and strength. This agent is most often applied as a precontest
or cutting steroid for bodybuilding purposes, and is
not viewed as an ideal bulking agent due to its lack of
estrogenicity. Athletes in sports where speed tends to be a
primary focus also find strong favor in
chlorodehydromethyltestosterone, obtaining a strong anabolic
benefit without having to carry around any extra water or fat
weight.
Administration (Women):
A common clinical dose of chlorodehydromethyltestosterone
is estimated to be 1-2.5 mg per day; actual prescribing
guidelines are unavailable. In the athletic arena, women
would commonly take a single 5 mg tablet per day, taken in
cycles lasting no more than 4-6 weeks to minimize
hepatotoxicity. Virilizing effects are unlikely at this level of
use. Much higher doses were often used with female athletes
in the former GDR doping program, but often to detriment of
strong virilizing side effects.
Availability:
Chlorodehydromethyltestosterone has been unavailable as a
prescription drug product in Germany (the sole country of
manufacture for most of its history) since 1994. A very small
number of pharmaceutical companies have marketed the drug
since, mainly in less regulated markets of Eastern Europe and
Asia, where black market demand still influences production.
In reviewing some of the remaining pharmaceutical products
and recent changes on the global pharmaceutical market, we
have made the following observations.
Balkan Pharmaceuticals (Moldova) makes the product
Turanabol. It is prepared in 10 mg tablets, 20 tablets per foil
and plastic strip.
By William Llewellyn

Presser · Apr 24, 2016

has anyone seen turinabol as injectable? not that i would wan that, i would much rather prefer oral tbol, but thought i would ask if people actually make this into an injectable steroid as well.

it sounds perfect to add to my propionate, trenbolone acetate and igf-1 lr3 cycle

Masher59 · Apr 24, 2016

I haven't seen it as an inject.

Presser · Apr 25, 2016

nor have i, but considering their always calling it oral turinabol as if they need to make a distinction between that and injectable, so i thought i would ask

Presser · Apr 26, 2016

tbol at 5mg daily sounds just right for a female competitor if you ask me.

Any women have experience running turinabol before?

akn · May 12, 2016

jolt · May 12, 2016

That would be the shit or mixed with anavar turanvar mix 50

Presser · May 13, 2016

jolt said:
That would be the shit or mixed with anavar turanvar mix 50

nice! lol, or anavol , nah i like your better lol,or turinavar

OxandroChlorode , sorry obsessed with it now lol,

Oral Turinabol (chlorodehydromethyltestosterone) anabolic steroid profile and dosage

akn

Musclechemistry Member

Presser

Admin

Masher59

MuscleChemistry Registered Member

Presser

Admin

Presser

Admin

akn

Musclechemistry Member

jolt

Banana

Presser

Admin

Similar threads