1. #1
    MuscleChemistry Registered Member Board Certified Psy.D

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    Default How to make your own testosterone!!!

    Man I wish!!LOL But hey, I'm getting up there in age, maybe I can get on HRT soon. Testosterone is synthesized from androstenedione, a product of dehydroepiandrosterone (DHEA) and progesterone, both of which are products of pregnenolone and cholesterol. And that's all I know. Just wish I could whip it up in my kitchen.

    https://www.musclechemistry.com/uploa...ersions-forum/
    Last edited by Presser; 02-26-2014 at 09:44 AM.
     

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    well, its a start...

    Cant we find some smart dude and instead of beating him up to fund our gear habit, we can just have him make it for us??

    it would be a hell of a lot less painful for him... just say'n..
     

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    hey... mikey's here!!
     

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    Up there in age - your age says 29 - that is in your prime bro.!!! lol
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    Yeah, but getting closer to that 30 mark is just getting depressing. You know how when you're a kid and you think of when you will be thirty how you will be "grown up", different, it'll be the future, things will be better. Well, one day you wake up and your almost thirty and your like, "Fuck, I'm the same dude!!" No one really grows up, if you were rich you'd be doing the same shit you were doing when you were 18!! The only difference when you get older is you get tired from work.LOL I'm all for the MuscleChemistry Lab Slave Boy. Make my gear bitch!!!!LOL
    But honestly, one of the HRT clinics I know of will consider you at age 29/30. But even on HRT, you are looking at 100-200mg/wk tops. Better than nothing, but if it were my only source I'd like at least 500mg/wk.LOL
     

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    Quote Originally Posted by Cracker69
    Yeah, but getting closer to that 30 mark is just getting depressing.
    shit how do you think mcgaret feels? he is now approaching almost 400 years old, his hrt therapy makes him only look about 200 though...
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    I am the irishman your mother warned you about.....

    I dont have a girlfreind but i know a girl who would get really mad at me if she heard me say that...

    Disclaimer - My comments in no way promote the use of androgenic/anabolic steroids and/or any prescription drug without a physician's prescription. All my comments, questions and referrals are striclty for entertainment purposes only!

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    lmao at IP im still young and im gonna be young till i hit 50 then ill consider myself a bit old.
    All statements from Get_Swole are strictly fictional none of the statements should be taken seriously or literally.

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    Fuck 30 !!!! Its the end of the world for me! Thats why I only date girls between 18 and 22 it will make you feel so much younger too! And you cant find a body of an 18 year old on a girl in their late 20s or early 30s no matter what you hear. And that experienced thing is bullshit to, I have had more 18 year olds rock me like a porn star !!! FACT!
     

  9. #9
    saudades
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    Quote Originally Posted by Cracker69
    Man I wish!!LOL But hey, I'm getting up there in age, maybe I can get on HRT soon. Testosterone is synthesized from androstenedione, a product of dehydroepiandrosterone (DHEA) and progesterone, both of which are products of pregnenolone and cholesterol. And that's all I know. Just wish I could whip it up in my kitchen.
    I feel the same thing, bro. I wish I could do that, too, especially since I'm about 10 years older than you.
     

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    I would just think that if testosterone is synthesized from androstenedione then there would be some way of actually converting it so that the final product is testosterone, so that we may be able to make our own injectables simply from buying a prohormone. I don't know if it's possible, or if it would be too in depth for an average person to understand, or have the equipment necessary, but it would be interesting to know the process that the manufactureres use to produce our stuff.
     

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    Well, since andro is now banned you would have to start with something that isn't watched say DHEA. Let me see what I can find.
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    saudades
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    That guy Patrick Arnold probably knew how to do it.
     

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    Default Looks like it was synthesized from cholesterol orignally

    Testosterone

    Testosterone is a steroid hormone from the androgen group. In mammals, testosterone is primarily secreted in the testes of males and the ovaries of females, although small amounts are also secreted by the adrenal glands. It is the principal male sex hormone and an anabolic steroid.

    In both men and women, testosterone plays a key role in health and well-being as well as in sexual functioning. Examples include enhanced libido, increased energy, increased production of red blood cells and protection against osteoporosis. On average, an adult human male body produces about forty to sixty times more testosterone than an adult female body, but females are more sensitive to the hormone.[1] However the overall ranges for male and female are very wide, such that the ranges actually overlap at the low end and high end respectively.


    History

    A Testicular action was linked to circulating blood fractions—now understood to be a family of androgenic hormones—in the early work on castration and testicular transplantation in fowl by Arnold Adolph Berthold (1803–1861). Research on the action of testosterone received a brief boost in 1889, when the Harvard professor Charles-Édouard Brown-Séquard (1817–1894), then in Paris, self-injected subcutaneously a “rejuvenating elixir” consisting of an extract of dog and guinea pig testicle. He reported in The Lancet that his vigor and feeling of wellbeing were markedly restored but, predictably, the effects were transient (and likely based on placebo), and Brown-Séquard’s hopes for the compound were dashed. Suffering the ridicule of his colleagues, his work on the mechanisms and effects of androgens in human beings was abandoned by Brown-Séquard and succeeding generations of biochemists for nearly 40 years.

    The trail remained cold until the University of Chicago’s Professor of Physiologic Chemistry, Fred C. Koch, established easy access to a large source of bovine testicles—the Chicago stockyards—and to students willing to endure the ceaseless toil of extracting their isolates. In 1927, Koch and his student, Lemuel McGee, derived 20mg of a substance from a supply of 40 pounds of bovine testicles that, when administered to castrated roosters, pigs and rats, remasculinized them.[2] The group of Ernst Laqueur at the University of Amsterdam purified testosterone from bovine testicles in a similar manner in 1934, but isolation of the hormone from animal tissues in amounts permitting serious study in humans was clearly not feasible until three European pharmaceutical giants—Schering (Berlin, Germany), Organon (Oss, Netherlands) and Ciba (Basel, Switzerland)—began full-scale steroid research and development programs in the 1930’s.

    The Organon group in the Netherlands were the first to isolate the hormone, identified in a May 1935 paper "On Crystalline Male Hormone from Testicles (Testosterone)" by Karoly Gyula David, E. Dingemanse, J. Freud and Ernst Laqueur. They named the hormone testosterone, from the stems of testicle and sterol, and the suffix of ketone. The structure was worked out by Schering’s Adolf Butenandt (1903–1995).

    The chemical synthesis of testosterone was achieved in August that year, when Butenandt and G. Hanisch published a paper describing "A Method for Preparing Testosterone from Cholesterol." Only a week later, the Ciba group in Zurich, Leopold Ruzicka (1887–1976) and A. Wettstein, announced a patent application in a paper "On the Artificial Preparation of the Testicular Hormone Testosterone (Androsten-3-one-17-ol)." These independent partial syntheses of testosterone from a cholesterol base earned both Butenandt and Ruzicka the joint 1939 Nobel Prize in Chemistry.[3] Testosterone was identified as 17β-hydroxandrost-4-en-3-one (C19H28O2), a solid polycyclic alcohol with a hydroxyl group at the 17th carbon atom. This also made it obvious that additional modifications on the synthesized testosterone could be made, i.e., esterification and alkylation.

    The partial synthesis in the 1930s of abundant, potent testosterone esters permitted the characterization of the hormone’s effects, so that Kochakian and Murlin (1936) were able to show that testosterone raised nitrogen retention (a mechanism central to anabolism) in the dog, after which Charles Kenyon’s group[4] was able to demonstrate both anabolic and androgenic effects of testosterone propionate in eunuchoidal men, boys, and women. The period of the early 1930s to the 1950s has been called "The Golden Age of Steroid Chemistry",[5] and work during this period progressed quickly. Research in this golden age proved that this newly synthesized compound—testosterone—or rather family of compounds (for many derivatives were developed from 1940 to 1960), was a potent multiplier of muscle, strength, and wellbeing.[6]



    Natural


    Human steroidogenesis, showing testosterone near bottom.

    Like other steroid hormones, testosterone is derived from cholesterol. The largest amounts of testosterone are produced by the testes in men. It is also synthesized in far smaller quantities in women by the thecal cells of the ovaries, by the placenta, as well as by the zona reticularis of the adrenal cortex in both sexes.

    In the testes, testosterone is produced by the Leydig cells. The male generative glands also contain Sertoli cells which require testosterone for spermatogenesis. Like most hormones, testosterone is supplied to target tissues in the blood where much of it is transported bound to a specific plasma protein, sex hormone binding globulin (SHBG).

    Artificial

    Testosterone is synthesizable in almost unlimited quantities. Furthermore, there are two possible modifications on it, giving it further abilities. First, it can be esterified, permitting a long-lasting effect when injected into the body. Second, it can be alkylated, permitting oral intake instead of injection.



    Esterification

    The second importance of the hydroxyl side chain at the C-17 position is that it can not only be esterified, but it can also be alkylated (by Alkylation permits oral steroids, substitution of an ethyl or methyl group for the hydroxyl group). the so-called “17-aa” or alkylated family of androgens such as methyl testosterone, which can be taken up by the digestive tract, and so be easily administered in pill form.


    In general, androgens promote protein synthesis and growth of those tissues with androgen receptors. Testosterone effects can be classified as virilizing and anabolic effects, although the distinction is somewhat artificial, as many of the effects can be considered both.
    • Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.
    • Virilizing effects include maturation of the sex organs, particularly the penis and the formation of the scrotum in unborn children, and after birth (usually at puberty) a deepening of the voice, growth of the beard and axillary hair. Many of these fall into the category of male secondary sex characteristics.

    Testosterone effects can also be classified by the age of usual occurrence. For postnatal effects in both males and females, these are mostly dependent on the levels and duration of circulating free testosterone.



    Adult testosterone effects

    Adult testosterone effects are more clearly demonstrable in males than in females, but are likely important to both sexes. Some of these effects may decline as testosterone levels decline in the later decades of adult life.
    • Maintenance of muscle mass and strength [8]
    • Maintenance of bone density and strength
    • Libido and clitoral engorgement/penile erection frequency.
    • Mental and physical energy
    • The most recent and reliable studies have shown that testosterone does not cause Prostate cancer, but that it can increase the rate of speed of any existing prostate cancer.[citation needed] Recent studies have also shown its importance in maintaining cardio vascular health.[citation needed]
    • Increase eumelanin and reduce pheomelanin[citation needed]

    Testosterone regulates the population of thromboxane A2 receptors on megakaryocytes and platelets and hence platelet aggregation in humans ( Ajayi and Halushka 2005, Ajayi et al 1995 ).



    Effects on the brain

    As testosterone affects the entire body (often by enlarging; men have bigger hearts, lungs, liver, etc.), the brain is also affected by this "sexual" advancement; the enzyme aromatase converts testosterone into estradiol that is responsible for masculinization of the brain in a male fetus.

    There are some differences in a male and female brain (the result of different testosterone levels); a clear difference is the size, the male human brain is on average larger, however in females (who generally do not have as high testosterone levels) the corpus callosum is proportionally larger. This means that the effect of testosterone is a greater overall brain volume, but a decreased connection between the hemispheres.[9]

    A study conducted in 1996 found no effects on mood or behavior from the administration of supraphysiologic doses of Testosterone for 10 weeks to healthy men.[10]

    The literature suggests that attention, memory, and spatial ability are key cognitive functions affected by testosterone in humans, though the literature is rather sparse. Preliminary evidence suggests that low testosterone levels may be a risk factor for cognitive decline and possibly for dementia of the Alzheimer’s type,[11] a key argument in Life Extension Medicine for the use of testosterone in anti-aging therapies. Much of the literature, however, suggests a curvilinear or even quadratic relationship between spatial performance and circulating testosterone,[12] where both hypo- and hypersecretion of circulating androgens have negative effects on cognition and cognitively-modulated aggressivity, as detailed above.

    Contrary to what has been postulated in outdated studies and by certain sections of the media, aggressive behaviour is not typically seen in hypogonadal men who have their testosterone replaced adequately to the eugonadal/normal range. In fact aggressive behaviour has associated with hypogonadism and low testosterone levels and it would seem as though supraphysiological and low levels of testosterone and hypogonadism cause mood disorders and aggressive behaviour, with eugondal/normal testosterone levels being important for mental well-being. Testosterone depletion is a normal consequence of aging in men. One consequence of this is an increased risk for the development of Alzheimer’s Disease (Pike et al, 2006, Rosario 2004).



    Mechanism

    The effects of testosterone in humans and other vertebrates occur by way of two main mechanisms: by activation of the androgen receptor (directly or as DHT), and by conversion to estradiol and activation of certain estrogen receptors.

    Free testosterone (T) is transported into the cytoplasm of target tissue cells, where it can bind to the androgen receptor, or can be reduced to 5α-dihydrotestosterone (DHT) by the cytoplasmic enzyme 5-alpha reductase. DHT binds to the same androgen receptor even more strongly than T, so that its androgenic potency is about 2.5 times that of T.[citation needed] The T-receptor or DHT-receptor complex undergoes a structural change that allows it to move into the cell nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects. It is important to note that if there is a 5-alpha reductase deficiency, the body (of a human) will continue growing into a female with testicles.

    Androgen receptors occur in many different vertebrate body system tissues, and both males and females respond similarly to similar levels. Greatly differing amounts of testosterone prenatally, at puberty, and throughout life account for a share of biological differences between males and females.

    The bones and the brain are two important tissues in humans where the primary effect of testosterone is by way of aromatization to estradiol. In the bones, estradiol accelerates maturation of cartilage into bone, leading to closure of the epiphyses and conclusion of growth. In the central nervous system, testosterone is aromatized to estradiol. Estradiol rather than testosterone serves as the most important feedback signal to the hypothalamus (especially affecting LH secretion). In many mammals, prenatal or perinatal "masculinization" of the sexually dimorphic areas of the brain by estradiol derived from testosterone programs later male sexual behavior.

    The human hormone testosterone is produced in greater amounts by males, and less by females. The human hormone estrogen is produced in greater amounts by females, and less by males. Testosterone causes the appearance of masculine traits (i.e deepening voice, pubic and facial hairs, muscular build, etc.) Like men, women rely on testosterone to maintain libido, bone density and muscle mass throughout their lives. In men, inappropriately high levels of estrogens lower testosterone, decrease muscle mass, stunt growth in teenagers, introduce gynecomastia, increase feminine characteristics, and decrease susceptibility to prostate cancer, reduces libido and causes erectile dysfunction and can cause excessive sweating and hot flushes. However an appropriate amount of estrogens is required in the male in order to ensure well-being, bone density, libido, erectile function etc.



    Therapeutic use



    Routes of administration

    There are many routes of administration for testosterone. Forms of testosterone for human administration currently available in North America include injectable (such as testosterone cypionate or testosterone enanthate in oil), oral,[13] buccal,[14] transdermal skin patches, and transdermal creams or gels.[15] In the pipeline are "roll on" methods and nasal sprays.



    Indications

    The original and primary use of testosterone is for the treatment of males who have too little or no natural endogenous testosterone production—males with hypogonadism. Appropriate use for this purpose is legitimate hormone replacement therapy, which maintains serum testosterone levels in the normal range.

    However, over the years, as with every hormone, testosterone or other anabolic steroids has also been given for many other conditions and purposes besides replacement, with variable success but higher rates of side effects or problems. Examples include infertility, lack of libido or erectile dysfunction, osteoporosis, penile enlargement, height growth, bone marrow stimulation and reversal of anemia, and even appetite stimulation. By the late 1940s testosterone was being touted as an anti-aging wonder drug (e.g., see Paul de Kruif's The Male Hormone). Decline of testosterone production with age has led to a demand for Androgen Replacement Therapy.

    To take advantage of its virilizing effects, testosterone is often administered to transmen as part of the hormone replacement therapy, with a "target level" of the normal male testosterone level. Like-wise, transwomen are sometimes prescribed anti-androgens to decrease the level of testosterone in the body and allow for the effects of estrogen to develop.

    Women use testosterones to treat low libido, often a symptom or outcome of hormonal contraceptive use. Women may also use testosterone therapies to treat or prevent loss of bone density, muscle mass and to treat certain kinds of depression and low energy state. Women on testosterone therapies may experience an increase in weight without an increase in body fat due to changes in bone and muscle density. Most undesired effects of testosterone therapy in women may be controlled by hair-reduction strategies, acne prevention, etc.

    There is a myth that exogenous testosterone can more or less definitively be used for male birth control. However, the vast majority of physicians will agree that to prescribe exogenous testosterone for this purpose is inappropriate. But, perhaps more important, many men found this, in first-hand experience, to be untrue or at least, unreliable.

    Some drugs specifically target testosterone as a way of treating certain conditions. For example, finasteride inhibits the conversion of testosterone into dihydrotestosterone (DHT), a metabolite which is more potent than testosterone. By lowering the levels of dihydrotestosterone, finasteride may be used for various conditions associated with androgens, such as benign prostatic hyperplasia (BPH) and androgenetic alopecia (male-pattern baldness). That said there are many men who have complained of long lasting or permanent adverse effects resulting from the use of finasteride and Dr Eugene Shippen has spoken for many years of finasteride causing a difficult to treat form of hypogonadism in some men.).





    Athletic use

    Testosterone may be administered to an athlete in order to improve performance, and is considered to be a form of doping in most sports. There are several application methods for testosterone, including intramuscular injections, transdermal gels and patches, and implantable pellets.

    Anabolic steroids (of which testosterone is one) have also been taken to enhance muscle development, strength, or endurance. They do so directly by increasing the muscles' protein synthesis. As a result, muscle fibers become larger and repair faster than the average person's. After a series of scandals and publicity in the 1980s (such as Ben Johnson's improved performance at the 1988 Summer Olympics), prohibitions of anabolic steroid use were renewed or strengthened by many sports organizations. Testosterone and other anabolic steroids were designated a "controlled substance" by the United States Congress in 1990, with the Anabolic Steroid Control Act.[17] The levels of testosterone abused in sport greatly exceed the quantities of the steroid that are prescribed for medical use in hypogonadism. It is the supraphysiological doses and ultra high levels of testosterone that bring with it many undesirable effects and potential long term adverse health effects. Coupled with the nature of cheating in sport, this is seen as being a seriously problematic issue in modern sport, particularly given the lengths to which athletes and professional laboratories go to in trying to conceal such abuse from sports regulators. Steroid abuse once again came into the spotlight recently as a result of the Chris Benoit double murder-suicide in 2007, and the media frenzy surrounding it - however there has been no evidence indicating steroid use as a contributing factor.



    Changes during aging

    Testosterone levels decline gradually with age in human beings. The clinical significance of this decrease is debated (see andropause). There is disagreement about if and when to treat aging men with testosterone replacement therapy. The American Society of Andrology's position is that testosterone therapy "is indicated when both clinical symptoms and signs suggestive of androgen deficiency and decreased testosterone levels are present". The American Association of Clinical Endocrinologists says "Hypogonadism is defined as a free testosterone level that is below the lower limit of normal for young adult control subjects. Previously, age-related decreases in free testosterone were once accepted as normal. Currently, they are not considered normal....Patients with low-normal to subnormal range testosterone levels warrant a clinical trial of testosterone."[18]

    There isn't total agreement on the threshold of testosterone value below which a man would be considered hypogonadal. (Currently there are no standards as to when to treat women.) Testosterone can be measured as "free" (that is, bioavailable and unbound) or more commonly, "total" (including the percentage which is chemically bound and unavailable). In the United States, male total testosterone levels below 300 to 400 ng/dl from a morning sample are generally considered low.[citation needed] However these numbers are typically not age-adjusted, but based on an average of a test group which includes elderly males with low testosterone levels.[citation needed] Therefore a value of 300 ng/dl might be normal for a 65 year old male, but not normal for a 30 year old.[citation needed] Identification of inadequate testosterone in an aging male by symptoms alone can be difficult. The signs and symptoms are non-specific, and might be confused with normal aging characteristics, such as loss of muscle mass and bone density, decreased physical endurance, decreased memory ability[citation needed] and loss of libido.

    Replacement therapy can take the form of injectable depots, transdermal patches and gels, subcutaneous pellets and oral therapy. Adverse effects of testosterone supplementation include minor side effects such as acne and oily skin, and more significant complications such as increased hematocrit which can require venipuncture in order to treat, exacerbation of sleep apnea and acceleration of pre-existing prostate cancer growth. Exogenous testosterone also causes suppression of spermatogenesis and can lead to infertility.[19] It is recommended that physicians screen for prostate cancer with a digital rectal exam and PSA (prostate specific antigen) level prior to initiating therapy, and monitor hematocrit and PSA levels closely during therapy.

    Appropriate testosterone therapy can prevent or reduce the likelihood of osteoporosis, type 2 diabetes, cardio-vascular disease (CVD), obesity, depression and anxiety and the statistical risk of early mortality. Low testosterone also brings with it an increased risk for the development of Alzheimer’s Disease (Pike et al, 2006, Rosario 2004).

    Large scale trials to assess the efficiency and long-term safety of testosterone are still lacking. Many caution against embracing testosterone replacement, whilst others embrace the advantages that the steroid seems to offer.
    Last edited by Presser; 11-19-2015 at 09:51 AM.
     

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    Yeah it would just be the best thing in the world if we all could just brainstorm and figure this out. Probably a stupid idea on my part and I'm sure if it could be done, someone would have it figured out by now, but damn it would be nice. And who's Patrick Arnold?
     

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    The chemist busted in the Balco disaster.

    It looks like it shouldn't be too difficult. DHEA + 17Beta-Hydroxy dehydrogenase reaction > Androstandiol + 3Beta-Hydroxy dehydrogenase reaction > Testosterone.

    2 steps from DHEA to Test. Look at the chemical structure/shapes. They are very similar.
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    Im going to start a batch in my bathtub now - I wonder if I should clean it first??
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    Quote Originally Posted by mcgaret
    Im going to start a batch in my bathtub now - I wonder if I should clean it first??
    where would we make our potato booze then?
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    I am the irishman your mother warned you about.....

    I dont have a girlfreind but i know a girl who would get really mad at me if she heard me say that...

    Disclaimer - My comments in no way promote the use of androgenic/anabolic steroids and/or any prescription drug without a physician's prescription. All my comments, questions and referrals are striclty for entertainment purposes only!

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    In the trash can...You just need one with the metal lids. lol.
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    You guys can make the alcohol, I'll make the testosterone. Here's some more interesting info.

    It is important to note at this point that all forms of prescription testosterone-- whether they are "bioidentical" or "synthetic"-- are created in laboratories using chemical means. The vast majority of prescription testosterone (cream, gel, injectable, patch, subcutaneous, etc.) is derived from plant sources such as soybeans and yams. Soybeans and yams are natural substances that are put through a chemical synthesis in a laboratory setting to derive the end product of testosterone. Both bioidentical and non-bioidentical testosterone drugs are synthesized in this manner
     

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    I dont know man... I dont think i want to be the first test subject...lol.
     

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    Lab Forum Link Below since this thread keeps coming up on on first page of google and very first listing when searching on How to make your own testosterone so follow this link below for many recipe conversions and brews

    MuscleChemistry Lab Conversions Forum

    https://www.musclechemistry.com/uploa...pe-discussion/
    Last edited by Presser; 08-20-2016 at 05:36 PM.
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    How to make your own testosterone!!!

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    Steroid Homebrew Recipe forum link above is dead, here is the correct link to that steroid recipe forum with sticky threads making your own testosterone enanthate, propionate, cypionate, masteron recipe, nandrolone decanoate, equipoise home brew and every oral and injectable steroid recipe how to you can think of!

    https://www.musclechemistry.com/uploa...-recipe-forum/


    new link below
    https://www.musclechemistry.com/uploa...pe-discussion/
    Last edited by Presser; 08-20-2016 at 05:35 PM.
    How to make your own testosterone!!!

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    Thanks,bro. I am trying making oil myself.
     

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    Quote Originally Posted by bodybuilder2015 View Post
    Thanks,bro. I am trying making oil myself.
    Have you ever home brewed bro? Go to the home brew section and read the stickies. All you need to know is there.
     

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    Well, the organic synthesis is actually fairly interesting.....a few years back I came across an even more *interesting* pathway for the test base part of the synthesis - using cholesterol, turning it into cholesterol acetate, and then (bit fuzzy here) a week-long reaction in a solution of yeast with oxygen bubbling through it, if memory serves. I think there one one other reagent....I'd have to find the procedure again. The technique used the natural enzymes in the yeast to do all the messy synthetic work - then you extracted and recrystalized from methanol to get pure test. If you wanted to esterify it, it's a standard procedure in....piperidine? (again, haven't looked at the procedure in about 12 years...) Should dig it up again :P
     

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    well this thread got some fucking hit lol,
    How to make your own testosterone!!!

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    You can take DHEA and an anti estrogen to boost testosterone. Both can be purchased OTC. If you take DHEA 50mg twice a day do the same with an anti estrogen.
    This will block the estrogen receptors and deliver the testosterone converted to your system. Theres a research study in a Science Journal I read that was asking why DHEA wasn't banned along with Andro.
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    heres a couple steroid powder home brew recipe conversions to make your own testosterone and some testosterone enanthate, masteron enanthate, and Trenbolone enanthate combination blends into a 375 milligram per milliliter painless injectable steroid



    Blends

    Testosterone 600mg/mL Blend @ 20mL


    Testosterone Enathate powder - 12g (displaces approx. 10.2ml ~ 51% total volume)
    3%BA – 0.6mL
    10%BB – 2mL
    25%EO – 5mL
    11% Oil – 2.2mL



    Tren E 125mg / Mast E 125mg / Test E 125mg
    Blend of 375mg/m
    l

    10ml conversion

    TrenE 1.25g (1.06ml)
    MastE 1.25g (1.06ml)
    TestE 1.25g (1.06ml)
    3%BA (0.3ml)
    30%BB (3ml)
    Oil (3.6ml)

    Tren E 250mg / Mast E 250mg
    Blend of 500mg/ml


    10ml conversion

    TrenE 2.5g (2.125ml)
    MastE 2.5g (2.125ml)
    3%BA (0.3ml)
    30%BB (3ml)
    EO (1.5ml)
    Oil (1ml)
    How to make your own testosterone!!!

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    Quote Originally Posted by Cracker69 View Post
    Testosterone

    Testosterone is a steroid hormone from the androgen group. In mammals, testosterone is primarily secreted in the testes of males and the ovaries of females, although small amounts are also secreted by the adrenal glands. It is the principal male sex hormone and an anabolic steroid.

    In both men and women, testosterone plays a key role in health and well-being as well as in sexual functioning. Examples include enhanced libido, increased energy, increased production of red blood cells and protection against osteoporosis. On average, an adult human male body produces about forty to sixty times more testosterone than an adult female body, but females are more sensitive to the hormone.[1] However the overall ranges for male and female are very wide, such that the ranges actually overlap at the low end and high end respectively.


    History

    A Testicular action was linked to circulating blood fractions—now understood to be a family of androgenic hormones—in the early work on castration and testicular transplantation in fowl by Arnold Adolph Berthold (1803–1861). Research on the action of testosterone received a brief boost in 1889, when the Harvard professor Charles-Édouard Brown-Séquard (1817–1894), then in Paris, self-injected subcutaneously a “rejuvenating elixir” consisting of an extract of dog and guinea pig testicle. He reported in The Lancet that his vigor and feeling of wellbeing were markedly restored but, predictably, the effects were transient (and likely based on placebo), and Brown-Séquard’s hopes for the compound were dashed. Suffering the ridicule of his colleagues, his work on the mechanisms and effects of androgens in human beings was abandoned by Brown-Séquard and succeeding generations of biochemists for nearly 40 years.

    The trail remained cold until the University of Chicago’s Professor of Physiologic Chemistry, Fred C. Koch, established easy access to a large source of bovine testicles—the Chicago stockyards—and to students willing to endure the ceaseless toil of extracting their isolates. In 1927, Koch and his student, Lemuel McGee, derived 20mg of a substance from a supply of 40 pounds of bovine testicles that, when administered to castrated roosters, pigs and rats, remasculinized them.[2] The group of Ernst Laqueur at the University of Amsterdam purified testosterone from bovine testicles in a similar manner in 1934, but isolation of the hormone from animal tissues in amounts permitting serious study in humans was clearly not feasible until three European pharmaceutical giants—Schering (Berlin, Germany), Organon (Oss, Netherlands) and Ciba (Basel, Switzerland)—began full-scale steroid research and development programs in the 1930’s.

    The Organon group in the Netherlands were the first to isolate the hormone, identified in a May 1935 paper "On Crystalline Male Hormone from Testicles (Testosterone)" by Karoly Gyula David, E. Dingemanse, J. Freud and Ernst Laqueur. They named the hormone testosterone, from the stems of testicle and sterol, and the suffix of ketone. The structure was worked out by Schering’s Adolf Butenandt (1903–1995).

    The chemical synthesis of testosterone was achieved in August that year, when Butenandt and G. Hanisch published a paper describing "A Method for Preparing Testosterone from Cholesterol." Only a week later, the Ciba group in Zurich, Leopold Ruzicka (1887–1976) and A. Wettstein, announced a patent application in a paper "On the Artificial Preparation of the Testicular Hormone Testosterone (Androsten-3-one-17-ol)." These independent partial syntheses of testosterone from a cholesterol base earned both Butenandt and Ruzicka the joint 1939 Nobel Prize in Chemistry.[3] Testosterone was identified as 17β-hydroxandrost-4-en-3-one (C19H28O2), a solid polycyclic alcohol with a hydroxyl group at the 17th carbon atom. This also made it obvious that additional modifications on the synthesized testosterone could be made, i.e., esterification and alkylation.

    The partial synthesis in the 1930s of abundant, potent testosterone esters permitted the characterization of the hormone’s effects, so that Kochakian and Murlin (1936) were able to show that testosterone raised nitrogen retention (a mechanism central to anabolism) in the dog, after which Charles Kenyon’s group[4] was able to demonstrate both anabolic and androgenic effects of testosterone propionate in eunuchoidal men, boys, and women. The period of the early 1930s to the 1950s has been called "The Golden Age of Steroid Chemistry",[5] and work during this period progressed quickly. Research in this golden age proved that this newly synthesized compound—testosterone—or rather family of compounds (for many derivatives were developed from 1940 to 1960), was a potent multiplier of muscle, strength, and wellbeing.[6]



    Natural


    Human steroidogenesis, showing testosterone near bottom.

    Like other steroid hormones, testosterone is derived from cholesterol. The largest amounts of testosterone are produced by the testes in men. It is also synthesized in far smaller quantities in women by the thecal cells of the ovaries, by the placenta, as well as by the zona reticularis of the adrenal cortex in both sexes.

    In the testes, testosterone is produced by the Leydig cells. The male generative glands also contain Sertoli cells which require testosterone for spermatogenesis. Like most hormones, testosterone is supplied to target tissues in the blood where much of it is transported bound to a specific plasma protein, sex hormone binding globulin (SHBG).

    Artificial

    Testosterone is synthesizable in almost unlimited quantities. Furthermore, there are two possible modifications on it, giving it further abilities. First, it can be esterified, permitting a long-lasting effect when injected into the body. Second, it can be alkylated, permitting oral intake instead of injection.



    Esterification

    The second importance of the hydroxyl side chain at the C-17 position is that it can not only be esterified, but it can also be alkylated (by Alkylation permits oral steroids, substitution of an ethyl or methyl group for the hydroxyl group). the so-called “17-aa” or alkylated family of androgens such as methyl testosterone, which can be taken up by the digestive tract, and so be easily administered in pill form.


    In general, androgens promote protein synthesis and growth of those tissues with androgen receptors. Testosterone effects can be classified as virilizing and anabolic effects, although the distinction is somewhat artificial, as many of the effects can be considered both.
    • Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.
    • Virilizing effects include maturation of the sex organs, particularly the penis and the formation of the scrotum in unborn children, and after birth (usually at puberty) a deepening of the voice, growth of the beard and axillary hair. Many of these fall into the category of male secondary sex characteristics.

    Testosterone effects can also be classified by the age of usual occurrence. For postnatal effects in both males and females, these are mostly dependent on the levels and duration of circulating free testosterone.



    Adult testosterone effects

    Adult testosterone effects are more clearly demonstrable in males than in females, but are likely important to both sexes. Some of these effects may decline as testosterone levels decline in the later decades of adult life.
    • Maintenance of muscle mass and strength [8]
    • Maintenance of bone density and strength
    • Libido and clitoral engorgement/penile erection frequency.
    • Mental and physical energy
    • The most recent and reliable studies have shown that testosterone does not cause Prostate cancer, but that it can increase the rate of speed of any existing prostate cancer.[citation needed] Recent studies have also shown its importance in maintaining cardio vascular health.[citation needed]
    • Increase eumelanin and reduce pheomelanin[citation needed]

    Testosterone regulates the population of thromboxane A2 receptors on megakaryocytes and platelets and hence platelet aggregation in humans ( Ajayi and Halushka 2005, Ajayi et al 1995 ).



    Effects on the brain

    As testosterone affects the entire body (often by enlarging; men have bigger hearts, lungs, liver, etc.), the brain is also affected by this "sexual" advancement; the enzyme aromatase converts testosterone into estradiol that is responsible for masculinization of the brain in a male fetus.

    There are some differences in a male and female brain (the result of different testosterone levels); a clear difference is the size, the male human brain is on average larger, however in females (who generally do not have as high testosterone levels) the corpus callosum is proportionally larger. This means that the effect of testosterone is a greater overall brain volume, but a decreased connection between the hemispheres.[9]

    A study conducted in 1996 found no effects on mood or behavior from the administration of supraphysiologic doses of Testosterone for 10 weeks to healthy men.[10]

    The literature suggests that attention, memory, and spatial ability are key cognitive functions affected by testosterone in humans, though the literature is rather sparse. Preliminary evidence suggests that low testosterone levels may be a risk factor for cognitive decline and possibly for dementia of the Alzheimer’s type,[11] a key argument in Life Extension Medicine for the use of testosterone in anti-aging therapies. Much of the literature, however, suggests a curvilinear or even quadratic relationship between spatial performance and circulating testosterone,[12] where both hypo- and hypersecretion of circulating androgens have negative effects on cognition and cognitively-modulated aggressivity, as detailed above.

    Contrary to what has been postulated in outdated studies and by certain sections of the media, aggressive behaviour is not typically seen in hypogonadal men who have their testosterone replaced adequately to the eugonadal/normal range. In fact aggressive behaviour has associated with hypogonadism and low testosterone levels and it would seem as though supraphysiological and low levels of testosterone and hypogonadism cause mood disorders and aggressive behaviour, with eugondal/normal testosterone levels being important for mental well-being. Testosterone depletion is a normal consequence of aging in men. One consequence of this is an increased risk for the development of Alzheimer’s Disease (Pike et al, 2006, Rosario 2004).



    Mechanism

    The effects of testosterone in humans and other vertebrates occur by way of two main mechanisms: by activation of the androgen receptor (directly or as DHT), and by conversion to estradiol and activation of certain estrogen receptors.

    Free testosterone (T) is transported into the cytoplasm of target tissue cells, where it can bind to the androgen receptor, or can be reduced to 5α-dihydrotestosterone (DHT) by the cytoplasmic enzyme 5-alpha reductase. DHT binds to the same androgen receptor even more strongly than T, so that its androgenic potency is about 2.5 times that of T.[citation needed] The T-receptor or DHT-receptor complex undergoes a structural change that allows it to move into the cell nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects. It is important to note that if there is a 5-alpha reductase deficiency, the body (of a human) will continue growing into a female with testicles.

    Androgen receptors occur in many different vertebrate body system tissues, and both males and females respond similarly to similar levels. Greatly differing amounts of testosterone prenatally, at puberty, and throughout life account for a share of biological differences between males and females.

    The bones and the brain are two important tissues in humans where the primary effect of testosterone is by way of aromatization to estradiol. In the bones, estradiol accelerates maturation of cartilage into bone, leading to closure of the epiphyses and conclusion of growth. In the central nervous system, testosterone is aromatized to estradiol. Estradiol rather than testosterone serves as the most important feedback signal to the hypothalamus (especially affecting LH secretion). In many mammals, prenatal or perinatal "masculinization" of the sexually dimorphic areas of the brain by estradiol derived from testosterone programs later male sexual behavior.

    The human hormone testosterone is produced in greater amounts by males, and less by females. The human hormone estrogen is produced in greater amounts by females, and less by males. Testosterone causes the appearance of masculine traits (i.e deepening voice, pubic and facial hairs, muscular build, etc.) Like men, women rely on testosterone to maintain libido, bone density and muscle mass throughout their lives. In men, inappropriately high levels of estrogens lower testosterone, decrease muscle mass, stunt growth in teenagers, introduce gynecomastia, increase feminine characteristics, and decrease susceptibility to prostate cancer, reduces libido and causes erectile dysfunction and can cause excessive sweating and hot flushes. However an appropriate amount of estrogens is required in the male in order to ensure well-being, bone density, libido, erectile function etc.



    Therapeutic use



    Routes of administration

    There are many routes of administration for testosterone. Forms of testosterone for human administration currently available in North America include injectable (such as testosterone cypionate or testosterone enanthate in oil), oral,[13] buccal,[14] transdermal skin patches, and transdermal creams or gels.[15] In the pipeline are "roll on" methods and nasal sprays.



    Indications

    The original and primary use of testosterone is for the treatment of males who have too little or no natural endogenous testosterone production—males with hypogonadism. Appropriate use for this purpose is legitimate hormone replacement therapy, which maintains serum testosterone levels in the normal range.

    However, over the years, as with every hormone, testosterone or other anabolic steroids has also been given for many other conditions and purposes besides replacement, with variable success but higher rates of side effects or problems. Examples include infertility, lack of libido or erectile dysfunction, osteoporosis, penile enlargement, height growth, bone marrow stimulation and reversal of anemia, and even appetite stimulation. By the late 1940s testosterone was being touted as an anti-aging wonder drug (e.g., see Paul de Kruif's The Male Hormone). Decline of testosterone production with age has led to a demand for Androgen Replacement Therapy.

    To take advantage of its virilizing effects, testosterone is often administered to transmen as part of the hormone replacement therapy, with a "target level" of the normal male testosterone level. Like-wise, transwomen are sometimes prescribed anti-androgens to decrease the level of testosterone in the body and allow for the effects of estrogen to develop.

    Women use testosterones to treat low libido, often a symptom or outcome of hormonal contraceptive use. Women may also use testosterone therapies to treat or prevent loss of bone density, muscle mass and to treat certain kinds of depression and low energy state. Women on testosterone therapies may experience an increase in weight without an increase in body fat due to changes in bone and muscle density. Most undesired effects of testosterone therapy in women may be controlled by hair-reduction strategies, acne prevention, etc.

    There is a myth that exogenous testosterone can more or less definitively be used for male birth control. However, the vast majority of physicians will agree that to prescribe exogenous testosterone for this purpose is inappropriate. But, perhaps more important, many men found this, in first-hand experience, to be untrue or at least, unreliable.

    Some drugs specifically target testosterone as a way of treating certain conditions. For example, finasteride inhibits the conversion of testosterone into dihydrotestosterone (DHT), a metabolite which is more potent than testosterone. By lowering the levels of dihydrotestosterone, finasteride may be used for various conditions associated with androgens, such as benign prostatic hyperplasia (BPH) and androgenetic alopecia (male-pattern baldness). That said there are many men who have complained of long lasting or permanent adverse effects resulting from the use of finasteride and Dr Eugene Shippen has spoken for many years of finasteride causing a difficult to treat form of hypogonadism in some men.).





    Athletic use

    Testosterone may be administered to an athlete in order to improve performance, and is considered to be a form of doping in most sports. There are several application methods for testosterone, including intramuscular injections, transdermal gels and patches, and implantable pellets.

    Anabolic steroids (of which testosterone is one) have also been taken to enhance muscle development, strength, or endurance. They do so directly by increasing the muscles' protein synthesis. As a result, muscle fibers become larger and repair faster than the average person's. After a series of scandals and publicity in the 1980s (such as Ben Johnson's improved performance at the 1988 Summer Olympics), prohibitions of anabolic steroid use were renewed or strengthened by many sports organizations. Testosterone and other anabolic steroids were designated a "controlled substance" by the United States Congress in 1990, with the Anabolic Steroid Control Act.[17] The levels of testosterone abused in sport greatly exceed the quantities of the steroid that are prescribed for medical use in hypogonadism. It is the supraphysiological doses and ultra high levels of testosterone that bring with it many undesirable effects and potential long term adverse health effects. Coupled with the nature of cheating in sport, this is seen as being a seriously problematic issue in modern sport, particularly given the lengths to which athletes and professional laboratories go to in trying to conceal such abuse from sports regulators. Steroid abuse once again came into the spotlight recently as a result of the Chris Benoit double murder-suicide in 2007, and the media frenzy surrounding it - however there has been no evidence indicating steroid use as a contributing factor.



    Changes during aging

    Testosterone levels decline gradually with age in human beings. The clinical significance of this decrease is debated (see andropause). There is disagreement about if and when to treat aging men with testosterone replacement therapy. The American Society of Andrology's position is that testosterone therapy "is indicated when both clinical symptoms and signs suggestive of androgen deficiency and decreased testosterone levels are present". The American Association of Clinical Endocrinologists says "Hypogonadism is defined as a free testosterone level that is below the lower limit of normal for young adult control subjects. Previously, age-related decreases in free testosterone were once accepted as normal. Currently, they are not considered normal....Patients with low-normal to subnormal range testosterone levels warrant a clinical trial of testosterone."[18]

    There isn't total agreement on the threshold of testosterone value below which a man would be considered hypogonadal. (Currently there are no standards as to when to treat women.) Testosterone can be measured as "free" (that is, bioavailable and unbound) or more commonly, "total" (including the percentage which is chemically bound and unavailable). In the United States, male total testosterone levels below 300 to 400 ng/dl from a morning sample are generally considered low.[citation needed] However these numbers are typically not age-adjusted, but based on an average of a test group which includes elderly males with low testosterone levels.[citation needed] Therefore a value of 300 ng/dl might be normal for a 65 year old male, but not normal for a 30 year old.[citation needed] Identification of inadequate testosterone in an aging male by symptoms alone can be difficult. The signs and symptoms are non-specific, and might be confused with normal aging characteristics, such as loss of muscle mass and bone density, decreased physical endurance, decreased memory ability[citation needed] and loss of libido.

    Replacement therapy can take the form of injectable depots, transdermal patches and gels, subcutaneous pellets and oral therapy. Adverse effects of testosterone supplementation include minor side effects such as acne and oily skin, and more significant complications such as increased hematocrit which can require venipuncture in order to treat, exacerbation of sleep apnea and acceleration of pre-existing prostate cancer growth. Exogenous testosterone also causes suppression of spermatogenesis and can lead to infertility.[19] It is recommended that physicians screen for prostate cancer with a digital rectal exam and PSA (prostate specific antigen) level prior to initiating therapy, and monitor hematocrit and PSA levels closely during therapy.

    Appropriate testosterone therapy can prevent or reduce the likelihood of osteoporosis, type 2 diabetes, cardio-vascular disease (CVD), obesity, depression and anxiety and the statistical risk of early mortality. Low testosterone also brings with it an increased risk for the development of Alzheimer’s Disease (Pike et al, 2006, Rosario 2004).

    Large scale trials to assess the efficiency and long-term safety of testosterone are still lacking. Many caution against embracing testosterone replacement, whilst others embrace the advantages that the steroid seems to offer.
    solid article
    Thanks BEASTZ6 thanked for this post
    Likes jimbosmith316 liked this post
     
    How to make your own testosterone!!!

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    Good read Presser!
    Likes Presser liked this post
     

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    For some reason this reminds me of the Sherlock Holmes story where the guy was shooting up gorilla giz to "reverse his aging" and it made him like a literal "animal"

    "The Adventures of the Creeping Man"
    Thanks Presser thanked for this post
    Likes thudgens96, Presser liked this post
     

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    Quote Originally Posted by Dean Destructo View Post
    For some reason this reminds me of the Sherlock Holmes story where the guy was shooting up gorilla giz to "reverse his aging" and it made him like a literal "animal"

    "The Adventures of the Creeping Man"
    Never seen it, but if Gorilla Giz worked, I’d use it!
    How to make your own testosterone!!!

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    Quote Originally Posted by Powderguy View Post
    You can take DHEA and an anti estrogen to boost testosterone. Both can be purchased OTC. If you take DHEA 50mg twice a day do the same with an anti estrogen.
    This will block the estrogen receptors and deliver the testosterone converted to your system. Theres a research study in a Science Journal I read that was asking why DHEA wasn't banned along with Andro.
    Bro, I have low testosterone and my doctor want to do a myriad of tests become prescribing testosterone. Tests including prolactin,PSA,LH,FSH, MRI of my pituitary gland and Testicular ultra sound. What do you think of this? Is this overkill?
     

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    Quote Originally Posted by kin View Post
    Bro, I have low testosterone and my doctor want to do a myriad of tests become prescribing testosterone. Tests including prolactin,PSA,LH,FSH, MRI of my pituitary gland and Testicular ultra sound. What do you think of this? Is this overkill?
    just pm trtdoc here on our site if you legally need trt treatment. No hoops like this I assure you.
    How to make your own testosterone!!!

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    Try: 12.5g Testosterone Enanthate Powder 7.5ml of Benzyl Benzoate
     

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    Quote Originally Posted by Presser View Post
    just pm trtdoc here on our site if you legally need trt treatment. No hoops like this I assure you.
    Derek Wilson back in da house!
    How to make your own testosterone!!!

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    Quote Originally Posted by Presser View Post
    Derek Wilson back in da house!
    Geez that guy is so retarded
     

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    Quote Originally Posted by Dean Destructo View Post
    For some reason this reminds me of the Sherlock Holmes story where the guy was shooting up gorilla giz to "reverse his aging" and it made him like a literal "animal"

    "The Adventures of the Creeping Man"
    what the fuck, how have i never heard of this lol

    And why this thread is listed under "how to make testosterone from yams" is beyond me lmao
    How to make your own testosterone!!!

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    well leave it to me to bump up some old ass thread that went no where but crazy, but i got a good laugh again, never thought anyone would actually ask how to synthesize testosterone, i understand asking for compounding recipe to make injectable testosterone from powders, but never synthesizing the actual hormone from dhea and whatever else they listed.

    If your going to delv this deep into it, you might as well learn how to cook crystal meth from match sticks and cold meds lmao, theis far more money in that shit then testosterone lmao

    i am obviously kidding, please dont blow up your house with meth lab and blame presser from MC lmao
    How to make your own testosterone!!!

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    Quote Originally Posted by kin View Post
    Bro, I have low testosterone and my doctor want to do a myriad of tests become prescribing testosterone. Tests including prolactin,PSA,LH,FSH, MRI of my pituitary gland and Testicular ultra sound. What do you think of this? Is this overkill?
    testicular ultra sound? Lol
    How to make your own testosterone!!!

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