Monday, August 22, 2016

Human Growth Hormone

Human Growth Hormone

How to Use Human Growth 
Hormone (hGH) for Fat Loss
trenbolone-www.ok-biotech.comQ:“How can I use GH for fat loss? How about for mass gain, and what would be the differences if any in use?”
A: The first consideration really in GH use for fat loss is dosage. Individual tolerance of GH can vary widely, but broadly speaking, most can use up to 14 IU total per week without development of neuropathy (numbness, weakness, or pain from nerve compression due to growth of cartilage.) Some can tolerate much more, a few cannot tolerate even this amount. So far as I know everyone can tolerate at least 7 IU per week, and nearly everyone 10.5 IU/week, or an average of 1.5 IU/day.
As might be expected, the higher the weekly dose the greater the benefit on fat loss.
There’s a wide range of theories on timing of doses. I’m not persuaded by any of them and have seen good results from any of a wide range of methods. My inclination is that best results are from at least 1x/day per use, rather than for example taking 4 IU every two days. However, difference in fat loss results from individuals, or differences in the same individual at different times, are large enough and the difference between protocols seems small enough that I won’t insist that the at-least-daily use is better for fat loss. It does seem so to me, however.
I don’t think there’s importance in GH timing with regard to meals. Morning may be better than evening or later in the day due to possibly providing less suppression of natural GH production; at any rate results seem a little better this way. If wishing to time the injection after a workout, this also is a well-proven method.
If wishing to be in best condition by a particular date, it usually proves acceptable to increase dosage by 50% in the two weeks before that date. While that dosage may be above the acceptable long-term dosage, the time period is short enough that neuropathy usually doesn’t develop, and if it does it will prove reversible, again due to the short time period.

Thursday, August 18, 2016

Oral Turinabol CAS: 2446-23-3

Oral Turinabol

Oral Turinabol CAS: 2446-23-3


Oral-Turinabol (dehydrochloromethyltestosterone) is an oral anabolic steroid which is interesting principally for reasons other than its unexceptional performance. It can however meet some specific needs.

What Is Oral-Turinabol?

Oral Turinabol is, to some extent, enigmatic and prone to misunderstanding.

It is not simply a tablet version of injectable Turinabol, or an alkylated version of it. Nor, despite claims, is it an anabolic steroid developed specifically for doping. That claim results from confusion with mestanolone.

Structurally, it is Dianabol with an added chlorine at the -4 position, which has the predictable advantage of preventing aromatization.

Caution must be taken however when trying to arrive at conclusions about anabolic steroids from structure. Substituting an atom or chemical bond makes large changes to the entire shape rather than affecting only a single point. This can result in changes in properties beyond the predictable. An example would be if one tried to predict the properties of Dianabol from its structural relation to boldenone (they are the same except for the 19-methylation of Dianabol.) While the methylation does provide the predictable oral bioavailability, in actuality Dianabol’s other properties are such that one can’t reasonably call “oral boldenone.”

In the case of Oral Turinabol, due to the above structural relation to Dianabol it’s commonly called a dry version of it. Now if this were true though, one could tell no difference between using OT alone and using Dianabol plus aromatase inhibitor. There is considerable difference in practice however.

OT must be considered its own compound rather than simply as a dry Dianabol. That said, this popular description is not a bad first approximation. Simply be aware of its limitations.

History Of Oral Turinabol

Ordinarily in anabolic steroid profiles I don’t discuss history of the drugs, but here it’s worth making an exception.

OT received an East German patent in 1961 and was soon approved as a prescription drug. At the time, there was wide medical belief that anabolic steroids were useful for recovery from surgery, burns, or nearly any condition that caused substantial loss of bodyweight. Newly developed anabolic steroids were considered suitable even for women and children, as it was thought that synthetic modifications dissociated androgenic from anabolic effects.



In 1966, use of OT for athletic doping began. This drug became the principal cause of the obvious virilization of East German female athletes of the era, despite the theoretical belief in separation of effects. Women did not respond as the theories from rat testing had predicted.

Why did the East Germans choose this specific compound for athletic doping? The reason does not seem to be from superior performance to Western anabolic steroids, or from drug testing concerns. That did not become an issue until much later. And a particularly favorable side-effect profile seems unlikely as the reason, as no other anabolic steroid has such a thoroughly documented track record for adverse effect on health.

A key doping advantage of OT for the East Germans was that it was locally produced. This provided easy availability, economy, and secrecy. And it was effective enough, especially for female athletes (but then again, every anabolic steroid is.)

The fact that its bad side effect profile made it quite harmful to the athletes was irrelevant to the East German Communist regime. Many lives were destroyed, at least in the judgment of the unknowing female doping victims.

Why mention all this? First, this history has created a mystique, whether warranted or not. And second, it has provided us with a great deal of toxicological information. Last, one should be sure that if choosing the drug, the decision is not simply from the mystique. Being the old East German doping drug of choice should be irrelevant to whether an athlete or bodybuilder should choose it today. Instead it should be considered in terms of its positive and negative effects. Among available anabolic steroids, OT offers nothing outstanding here, though it’s certainly usable.

Dosing Of Oral Turinabol For Men

When Oral Turinabol is used in an anabolic steroid cycle, less than 20 mg per day will be an almost unnoticeable addition to a stack, or will be a very weak cycle if used alone. There is little point in exceeding 50 or 60 mg/day, as added anabolic effect will be small if any. And adverse side effects of excessive muscle pumps and/or blood pressure elevation are often at a tolerance limit at this point, while becoming excessive past it.

I don’t recommend combining OT with other oral anabolic steroids. Instead, when using OT and wishing to increase anabolism, one or more injectables should be added rather than another oral. A sufficient reason for this is that results are much better from combining an injectable rather than any other oral (with possible exception of oxandrolone.) Another reason is that at effective doses of OT, hepatotoxicity is already as high as can be considered reasonable. Another alkylated steroid should not be added.

Still another reason to not combine OT with other oral anabolic steroids in a stack with injectables is this: If Dianabol or Anadrol are included in the stack, then there’s no reason to also include OT. It will do nothing anabolically that they will not.

Oral Turinabol can be used alone with significant results for novice steroid users or for experienced users who have experienced losses and are regaining. However in general I don’t recommend oral only cycles, and this is no exception.

When using OT, dosing is preferably divided to twice per day, although once per day is acceptable.

Oral Turinabol For Women?

East German female athletes took OT at 5-15 mg per day for two to six weeks at a time. Aside from obvious virilization, many of these female athletes also suffered liver disease, heart disease, infertility, psychiatric issues, and even death. Oral Turinabol is proven not to be a safe anabolic steroid for women. I am not saying these consequences are inevitable, but rather that it’s a proven fact that the incidence rate of such consequences is very substantial.

Risk will exist for some women at doses less than 5 mg/day as well.

Nearly any anabolic steroid is better choice for women than OT.

Summary

Oral Turinabol is of interest mostly for its history, not its performance. When chosen, dosing range should be 20-60 mg/day, taken either once per day or preferably twice. It is usable by men, although there are better choices. OT is a very poor choice for women.


Wednesday, August 17, 2016

Cialis (Tadalifil)

Cialis (Tadalifil)

Cialis (Tadalafil) CAS: 171596-29-5


Cialis (Tadalifil citrate), a phosphodiesterase type 5 inhibitor, is used to treat erectile dysfunction (ED) and decreased libido in males.  Cialis works by aiding relaxation of blood vessels and increasing blood flow in the penis during sexual arousal, resulting in improved erectile function.  Cialis is much longer lasting than Viagra.  Effects can be felt anywhere between 36-48 hours.

Background

The FDA approved Cialis as a medicine for ED on November 21, 2003. It is available through prescription for those who are diagnosed with impotence.  In 1998, ICOS Corporation, and Eli Lilly and Company, began manufacturing Cialis, which is available orally in 5mg, 10mg and 20mg tablets.  It is also widely available by many research companies and underground labs.

Action

Tadalafil improves erectile function significantly, possibly increase testosterone through increased sexual activity, and is very safe.

There are limited side effects associated with its use.  The most common side effects are headache, upset stomach, back pain, and muscle aches, and usually subside with in a few hours.

Technical Data

In a six month study on men with erectile dysfunction ranging from mild to severe, 20 mgs of Cialis or placebo was administered to subjects as needed.  It was discovered that Tadalafil improved ED compared to placebo.  Ability to achieve erection and sucessful intercourse was 73% greater in those reciving Cialis verses the placebo group (1). Cialis was administered three times per week for an extended period of time, it was found to be extremely safe and very limited side effects were experienced, if any (1).

Cialis was also linked to increased testosterone levels in a one month study where testosterone levels were found to be significantly higher at the end of the month, due to increased sexual activity(2).

User Notes

How ironic. Some of the compounds which can be used to make men more physically attractive to women (Deca, Tren, etc…) can cause sexual dysfunction. Even more ironic is that many of the compounds which make them more attractive to us (Beer, Whiskey, etc…) can also do this.

Cialis is useful for these occasions…or during PCT when sexual dysfunction may occur.

Tadalifil citrate is the chemical name of active ingredient in Cialis. Cialis is a registered trademark of Lilly ICOS LLC in the United States and/or other countries.

References

1.A 6-month study of the efficacy and safety of tadalafil in the treatment of erectile dysfunction: a randomised, double-blind, parallel-group, placebo-controlled study in Australian men. Int J Clin Pract. 2005 Feb;59(2):143-9.
2.Type V phosphodiesterase inhibitor treatments for erectile dysfunction increase testosterone levels. Clin Endocrinol (Oxf). 2004 Sep;61(3):382-6.



Tuesday, August 16, 2016

Trenbolone will be soon used for hormone replacement therapy

Trenbolone will be soon used for 
hormone replacement therapy
Trenbolone is a steroid that is taken by bodybuilders for many years. Unfortunately, this drug has never been considered to be an effective drug for clinical purposes. It isn't approved for human usage by the U. S. Food and Drug Administration (FDA). Trenbolone has been demonized many times by media. A lot of articles have announced that this medication is quite dangerous. 
But recent studies have shown opposite facts. It is supposed that common attitude to this medicine can be soon changed. 
Joshua Yarrow and his colleagues from the University of Florida claim that this medicine can be taken as testosterone for hormone replacement therapy. The experts point out that it is an appropriate alternative preparation to testosterone for the purpose mentioned above. Results of studies conducted by these experts have been published in the American Journal of Physiology – Endocrinology and Metabolism. 
Moreover, the specialists assure that trenbolone enanthate has even some priorities over testosterone for certain persons. Bodybuilders know and support the statements linked with this product. It is known that testosterone aromatases. As for trenbolone, it is turned neither to estradiol, nor to dihydrotestosterone (DHT). That's why trenbolone doesn't lead to unwanted symptoms related to estrogen and DHT. 
Joshua Yarrow says about the studies led by him and his colleagues. Castrated rats have been given trenbolone enanthate. Even reduced dosages of this medication have enhanced their muscle size and kept bone mineral density. There have not seen such side reactions, as prostate enlargement or polycythemia in these lab rats. 
But too increased dosages of testosterone enanthate were required to cause the same anabolic effects in muscles as were caused by reduced dosages of trenbolone enanthate. But such negative consequences, as enlargement of prostate and increased hemoglobin accompanied the increased measures of testosterone enanthate. It is supposed by the researchers that trenbolone acts like selective androgen receptor modulators, causing anabolic effects in muscles and bones without androgenic adverse reactions. 
Professional competitive bodybuilders prefer taking trenbolone several weeks before competitions because it causes fat loss. Moreover, the studies have shown that the same measures of trenbolone have stronger lipolytic effects than those of testosterone. It has been determined that more trenbolone a person administers, the greater the fat loss is produced. 
Since trenbolone lacks aromatization, it is commonly taken together with such steroids, as testosterone, Dianabol or with another aromatizable steroid. The lack of aromatization leads trenbolone to disability to be used alone for testosterone replacement therapy. The non-aromatizable characteristic of this medicine is responsible for just partial protective effect of bones. 
Nevertheless, it is possible to make conclusion that additional studies are needed in order to apply trenbolone for hormone replacement therapy. 

Sunday, August 14, 2016

Do Halotestin, Oral-Turinabol and Methyltestosterone Have Any Advantages Over Dianabol, Anadrol, Anavar and Winstrol?

Do Halotestin, Oral-Turinabol and Methyltestosterone Have Any Advantages Over Dianabol, Anadrol, Anavar and Winstrol?
Q: “Why limit the oral choices in my cycles to Dianabol, Anadrol, oxandrolone, or Winstrol? I can get methyltestosterone, Halotestin, or Oral-Turinabol as well.”
A: I think it’s really not a question of limiting.
Combination simply for the sake of combination doesn’t improve results. In contrast, some specific combinations do help, where compounds work synergistically with each other.
These bases are already covered when having the oral anabolic steroids you first mention. Any additional oral anabolic steroid may be used, but when they are used, there’s not a point to adding them to the above. Instead, they might be replacements.
But they would be replacements for no particular reason. I don’t find a special advantage to any of these compounds. An exception certainly can be where experiencing a personal result. If for example an athlete has experienced enhanced endurance performance from Halotestin (most likely from effect on the CNS) then certainly it might be used again even though others may dislike it for water retention reasons. Likewise, if a lifter has found enhanced performance in the gym from methyltestosterone, high might continue to use it, although others might dislike it for its effect on liver values.
In the case of Halotestin, a likely reason for its particular adverse side effect profile is strong inhibition of an enzyme (11b-hydroxysteroid dehydrogenase 2) which acts to reduce the potency of cortisol. By increasing its effective activity, it could disturb electrolyte balance and cause water retention. Again, this doesn’t mean it can’t be used, but it’s a reason for it to not be in the first tier among oral anabolic steroids.
Oral-Turinabol might be used where a person wishes to use only a single oral steroid and get reasonable mass and strength gains. Generally I don’t see a reason to limiting to only oral use, let alone only one oral compound, but some do want to do it. I’d certainly recommend, for example, a Dianabol/oxandrolone stack instead, though if going oral-only, and even moreso I’d recommend a good injectable/oral stack.
In general, there seem more issues of water retention, adverse effect on blood lipid profiles, and worsened liver values with the latter steroids mentioned than the first group, but not to so great an extent as to rule them out. They simply are not my first choice, and nothing is lost by keeping choice within the first-mentioned orals.

Wednesday, August 10, 2016

99% High Purity Steroid Hormone Testosterone Enanthate Test E CAS 315-37-7

99% High Purity Steroid Hormone Testosterone Enanthate Test E CAS 315-37-7
99% High Purity Steroid Hormone Testosterone Enanthate Test E CAS 315-37-7
We are the best manufacturer of steroids plus other raw powders in China for many years(www.ok-biotech.com), good prices, high quanlity,best package methods, safety shippment, more important,we guarantee delivery so there will be not any loss after you order.
Product Description:

Testosterone enanthate is an ester of testosterone which is used for the treatment in males to treat primary hypogonadism (congenital or acquired) - testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, or orchidectomy.
Testosterone 250 USP injection provides testosterone enanthate, a derivative of the principal endogenous androgen testosterone, for intramuscular administration. The esterification of the 17 - beta -hydroxyl group increases the duration of the action of testosterone. Testosterone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus Testosterone 250 can be administered at intervals of 1 -2 weeks.
Testosterone 250 contains testosterone enanthate in a 10ml solution for injection (250mg testosterone enanthate / ml).Testosterone 250 is a clear, yellowish oily solution for intramuscular injection.

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Injectable Tamoxifen Citrate Nolvadex Anti Estrogen Steroids No Side Effects

Injectable Tamoxifen Citrate Nolvadex Anti Estrogen Steroids No Side Effects

email: smile@ok-biotech.com
skype: onsellsteroids
whatsapp: +8618924660950
www.ok-biotech.com

Nolvadex (tamoxifen citrate) is very comparable to Clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure.

Alias: Nolvadex;TAM
CAS No: 10540-29-1
Einecs No: 234-118-0
MF: C26H29NO
MW: 371.51 
Purity: 99%
Apperance: white to off-white powder
Usage: estrogen antagonist,antineoplastic


IMG_2218

Description:

Nolvadex (tamoxifen citrate) is very comparable to Clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure.

Applications:

Antitumor drugs raw material, suitable for breast cancer.It is not correct that Nolvadex reduces levels of estrogen: rather, it blocks estrogen from estrogen receptors and, in those tissues where it is an antagonist, causes the receptor to do nothing. Nolvadex isnotan anabolic steroid but is used to manage side effects from steroids.
Biological Activity: Estrogen receptor antagonist/partial agonist. Selective and potent inhibitor of mammalian sterol isomerase. Neuroprotective in female rats in vivo . Also high affinity agonist at the membrane estrogen receptor GPR30.


Specifications:

Test ItemsSpecificationTest Results
DescriptionWhite crystalline powderWhite crystalline powder
IdentificationIR , UV conformConform
Loss on drying≤0.5ml0.21ml
Residue on ignitionNot more than 0.2%0.06ml
IronNot more than 0.005%0.0018%
Heavy metalsNot more than 0.001%0.0006%
Related substances
Total: Not more than 1.0%
Individual: Not more than 0.5%
0.32%
0.14%
E-isomerNot more than 0.3%0.19%
Organic volatile impuritiesConformsConforms
Assay99.0~101.0%99.51%
ConclusionConform with USP30