Raw Steroid Powder Tibolone

Product Name: Tibolone
Alias: Livial,Liviella
CAS: 5630-53-5
EINECS: 227-069-1
MF: C26H34O4
MW: 312.45
Assay: 97.0%~103.0%
Grade: Pharmaceutical Grade
Appearance: White Crystalline Powder
Usage: Pharmaceutical Raw Materials

Usage

Tibolone can be used as pharmaceutical material, It is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women.

Tibolone Livial/Liviella is used mainly for treatment of endometriosis, as well as hormone replacement therapy in post-menopausal women. Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for ER alpha. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile. It has also been investigated as a possible treatment for female sexual dysfunction.

Tibolone is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women. It is a synthetic steroid that has the same activity as the female sex hormones estrogen and progesterone and the androgen testosterone. Tibolone helps restore hormonal balance in the body.

When estrogen levels are low tissues can slowly degenerate, as is experienced during menopause. In addition, low levels of estrogen can cause distressing symptoms such as hot flushes, night sweats, mood swings, reduced sex drive and vaginal dryness. Tibolone is broken down into three compounds which act in a similar way to the natural estrogen and progesterone found in the body. It restores plasma endorphin level in post-menopausal women and acts centrally to affect the thermo-regulatory system.

Raw Steroid Powder Stanolone

Product Name: Stanolone
Alias: Dihydrotestosterone; DHT
CAS: 521-18-6
EINECS: 208-307-3
MF: C19H30O2
MW: 290.4403
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Crystalline Powder
Density: 1.085g/cm3
Melting Point: 173-183°C
Boiling Point: 413.1°C at 760 mmHg
Flash Point: 176.4°C

Stanolone is a potent androgenic metabolite of testosterone. Stanolone is generated by a 5-alpha reduction of testosterone. Stanolone is thought to be approximately 30 times more potent than Testosterone because of increased affinity to the androgen receptor.

Stanolone is mainly formed in the testes, the hair follicles, the adrenal glands and the prostate gland. It is produced when testosterone interacts with an enzyme in the body. In the womb, Stanolone stimulates the development of male characteristics of the male embryo and fetus. During puberty, it is involved in developing other male characteristics such as body and facial hair and the deepening of the voice. Later in life, the level of Stanolone is usually much lower, and its presence can cause problems.

Stanolone For Bodybuilding

Stanolone used to be the athlete's favorite competition steroid since it helped to obtain a harder muscle through a lower fat content by increasing the androgen level without aromatizing. Numerous athletes used Stanolone during workouts for doping tested championships since the substance remains in the body for only a short time and the testosterone/epitestosterone value is not influenced. Another positive characteristic is that the injectable version is not liver toxic.

Today, however, Stanolone is rarely used by athletes. One reason for this is that almost all European and American compounds are no longer commercially available. The other reason is that most athletes use the still readily available Masteron which has similar effects. Neither the original nor a fake of Stanolone is available on the black market.

Stanolone Application

Unlike other androgens such as testosterone, Stanolone cannot be converted by the enzyme aromatase into an estrogen like estradiol. Therefore, it is frequently used in research settings to distinguish between the effects of testosterone caused by binding to the AR and those caused by testosterone's conversion to estradiol and subsequent binding to and activation of estrogen receptors.

Stanolone is used for chronic wasting disease, osteoporosis, severe infection and trauma, burn, etc caused by the negative nitrogen balance, promote the growth of premature infants and immature, etc. The fracture is not easy to heal. Hypercholesterolemia and postpartum depression can also be used.

Raw Steroid Powder Mibolerone

Product Name: Mibolerone
Alias: Cheque Drops
CAS: 3704-09-4
EINECS: 223-046-5
MF: C20H30O2
MW: 302.45
Grade: Pharmaceutical Grade
Appearance: White Crystalline Powder
Usage: Pharmaceutical Raw Materials
Melting Point: 168-171 dec.

Originally used to suppress ovulation of female dogs in heat, Mibolerone is one of the most harsh steroids in existence. It is approximately 5.9 times as anabolic, and 2.5 times as androgenic as Testosterone. Cheque drops provide a short adrenaline-like aggression rush in athletes when used immediately prior to a sporting event.  Due to its high androgenic properties, it is often the cause of progesterone related gynecomastia.

Steroid Action: Due to the short half-life of Mibolerone, it is most commonly used by athletes about 30-40 minutes before their sporting event. Cheque drops are placed under the athletes tongue, and effects including aggression, strength and adrenaline rush are felt rapidly.  The drug leaves the body with in approximately four hours.

As well as being one of the most androgenic compounds, mibolerone is also one of the most toxic.   The most common side effect is progesterone related gynecomastia because it is a 19 nor-androgen.    It can also severely affect liver function because it is a 17AA compound.  Use with other 17AA compounds can be extremely damaging to the liver.  If used in low doses (less than 2 weeks), there are very few, if any anabolic effects.  When used short term, natural testosterone will return to normal levels very quickly.  However, if use surpasses 2 weeks there is an extremely high risk for liver damage and natural testosterone suppression because it is an LH blocker. Also, this compound does not convert into estrogen; therefore, progesterone production is increased.

Known side effects of the compound are increased aggression, disturbed sleep patterns or insomnia, high blood pressure and severe liver damage.  It is highly dangerous if used by females.  Some female side effects include severe acne, cessation of the menstrual cycle, deepening of the voice, clitoral enlargement and vaginal secretion.  Effects of the drug will also be passed onto an unborn fetus.

In rats, Mibolerone has been shown to be both highly anabolic and androgenic. It was found to be 41 times more anabolic and 16 times more androgenic than methyltestosterone.  No estrogenic activity in mice was reported when when 1.0 mg per animal per day was administered.  It was also found to be anti-estrogenic in mice 10 mcg or less when subcutaneously tested against estradiol. A dose of 1,600,000mcg/kg was fatal in 50% of the rats.

User Notes: This is really nasty stuff. Basically, it's only good for increasing aggression just prior to an athletic event or before an intense training session. For most athletes, Methyltestosterone, Testosterone Suspension, or Halotestin is typically preferred for this purpose because Cheque Drops are rarely found on the black market.

Raw Steroid Powder Fluoxymesterone

Product Name: Fluoxymesterone
CAS: 76-43-7
EINECS: 200-961-8
MF: C20H29FO3
MW: 336.4409
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Crystalline Powder
Density: 1.22g/cm3
Melting Point: 240°C
Boiling Point: 474.2°C at 760 mmHg
Flash Point: 240.6°C

Powerful Anabolic-Androgenic Fluoxymesterone

Fluoxymesterone is a great hardener and cutter steroid for bodybuilders, although the side effects may make the benefits counter productive. One feature that is immediately noticed with Fluoxymesterone is the anabolic and androgenic rate which can only be described as extraordinary. 19x more anabolic and 8.5 more androgenic, that could be unbelievable!

In the bodybuilding world Fluoxymesterone is considered a very popular choice for power lifters and strength athletes, they comprise a majority of the users for this drugs compared to body builders. The reason behind is Fluoxymesterone's ability to give a strength boost a few weeks before weight lifting competitions.

Fluoxymesterone Benefits

One of the benefits of Fluoxymesterone is that it resists aromatization or conversion of testosterone and estrogen. For this reason, stacking with aromatase inhibitors or anti-estrogen drugs or with other forms of anabolic androgenic steroids is not typically necessary with Fluoxymesterone.

Fluoxymesterone Dosage

It is recommended that dosage of Fluoxymesterone be kept at 20mg a day for 4-6weeks, then from there you can try a higher dose. For purposes of added aggression keep the dosage at 10mg before workout.

Fluoxymesterone Side Effects

Fluoxymesterone is hepatoxic, it can cause potentially liver damage. Another side effect of Halotestin is the negative feedback it sends the Hypothalamic-pituitary testicular axis. This can lead to sexual dysfunction when endogenous testosterone becomes depressed.

To bring back testosterone to normal levels you can make use a combination of testosterone stimulants and estrogen receptor modulators.

Raw Steroid Powder Clostebol Acetate

Product Name: Clostebol Acetate
Alias: 4-Chlorotestosterone Acetate; Turinabol
CAS: 855-19-6
EINECS: 212-720-4
MF: C21H29ClO3
MW: 364.9062
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Crystalline Powder
Density: 1.19g/cm3
Boiling Point: 457.2°C at 760 mmHg
Flash Point: 155.7°C

Clostebol Acetate For Bodybuilding

Clostebol Acetate help growth of muscle mass and strength. For the most part, the gains in strength and muscle size that the user will experience while using Clostebol Acetate will be moderate. It is not an overly powerful drug and as such will not produce overly dramatic gains.

However with this comes the benefit that it is a relatively safe drug for use, including for women. When combined with other anabolic compounds many users will find that it will provide quality gains in lean mass while not causing estrogenic side effects such as excessive water retention or severe androgenic side effects. 

Clostebol Acetate Effects

Clostebol Acetate effects include maturation of the sex organs, particularly the penis and the formation of the scrotum in the fetus, 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

Clostebol Acetate can help cattle grow fat. Clostebol Acetate has high anabolic action and low androgenic activity, is devoid of estrogenic properties or progestative. Clostebol Acetate inhibits the secretion of pituitary gonadotropins.

Oral And Injectable Clostebol Acetate

Clostebol Acetate appears in several versions. Injectable, oral and even topical creams have all been produced. However, only the oral and injectable versions of the drug would be suitable for the purposes of strength athletes and bodybuilders.

The oral version of Clostebol Acetate is not 17 alpha alkylated like most other oral steroids. This means that the liver toxicity associated with the drug is far less then other steroids. However this also means that the amount of the drug that actually clears the system of the user and becomes active in the body is at a relatively low ratio to the amount that is administered. For this reason larger doses of the oral version of the drug must be ingested in comparison to the injectable.

The Clostebol Acetate injectable, as it name suggests, utilizes the acetate ester to help slow absorption of the drug into the blood stream. This ester has only two carbon atoms and is the quickest of the esters that is used commonly in the production of anabolic steroids. For this reason frequent injections are required when administering Clostebol Acetate.

Clostebol Acetate Dosage

In terms of the frequency needed for dosing, the oral version of the drug needs to be administered roughly twice per day to maintain some of the compound being active in the body of the user. For male users 25-70 milligrams per day should produce good results. For female users 10 milligrams per day would be a good starting point, with higher doses of course being negotiable once one knows how they tolerate the drug. 

As for the injectable version of Clostebol Acetate , injections every day or every other day are needed to maintain fairly consistent levels of the compound in the system of the user. 20-40 milligrams per day should be more then adequate for male users, remembering of course that the injectable version has to be administered at least every other day. 50 to 100 milligrams per week are seemingly the norm for most female users.