|Place of Origin:||China|
|Certification:||ISO 9001, USP,GMP|
|Minimum Order Quantity:||10g|
|Packaging Details:||Disguised package ; Foil bag|
|Delivery Time:||3-5 work days|
|Payment Terms:||Western Union, MoneyGram, T/T, bitcoin|
|Supply Ability:||Mass in stock|
|Package:||Disguised Package ; Foil Bag||MW:||302.45|
|Delivery Date:||3-5 Work Days|
raw testosterone powder,
testosterone based steroids
Appearance: white powder
Grade: Pharmaceutical grade
Package: Disguised package ; Foil bag
Delivery date: 3-5 work days
Model NO.: 65-04-3
Suitable for: Elderly, Adult
CAS No.: 65-04-3
Specification: GMP, SGS
HS Code: 2942000000
Certification: GMP, ISO 9001, USP, BP
17-methyl testosterone is one of the oldest available oral steroids. It is produced by many different manufacturers and is sold in many countries including the United States. It is quite androgens, with minimal metabolic effects. For motor use, methyltestosterone is usually used only to stimulate the power lifter and those who wish to improve their exercise.
Many 17-methyl testosterone tablets are sublingual (placed under the tongue) for faster absorption. These tabs can usually be identified by their significant citrus taste. Before you visit the gym, placing a few labels below the tongue may cause exercise. In addition, methyl testosterone provides little side effects other than androgen. It is quite toxic, raising liver enzymes and causing acne, men's breast development, attack and water retention is easy. If a person tolerates these side effects, methyltestosterone will provide some slight strength gain.
17-methyl testosterone is an artificial form of testosterone that is a naturally occurring sex hormone produced in human testes. A small amount of testosterone is also produced in women's ovaries and adrenal glands.
The combination of estrogen and 17-methyltestosterone for the treatment of menopausal symptoms, such as hot flushes, and vaginal dryness, burning and irritation. This drug can also be used for purposes not listed in this drug guide.
17α-methyl testosterone is a synthetic androgen that is affinity for androgen receptors. 17α-methyl testosterone is widely used as a component of hormone replacement therapy. Previous reports indicate that, contrary to testosterone, 17α-methyl testosterone is not aromatic. However, 17α-methyl testosterone can still affect local estrogen formation by modulating aromatase expression or by inhibiting aromatase action. Both of these possibilities have important clinical implications.
To evaluate the effect of 17α-methyltestosterone on the expression and activity of aromatase, we tested chorionic carcinoma Jar cell lines, cell lines expressing high levels of P450 aromatase and macrophage-like THP-1 cells expressing aromatase Experience differentiation. We found that 17α-methyltestosterone inhibited aroma activity in a dose-dependent manner in both cell lines. The inhibition curve was similar to that of letrozole and was completely inhibited at 10 (-4) M17α-methyltestosterone and was determined by tritium release assay.
17α-methyl testosterone has no detectable effect on the expression of aromatase RNA and Jar cells. The undifferentiated THP-1 cells had no aromatase activity and did not show the effect of 17α-methyltestosterone, but the differentiated THP-1 (macrophage-like) cells had the same effect on 17α-methyltestosterone as observed in Jar cells Of the similar aromatase activity. The Lineweaver-Burke graph shows that 17α-methyl testosterone is a competitive aromatase inhibitor. Our results for the first time show that 17α-methyl testosterone as an aromatase inhibitor. These findings are related to the understanding of the effect of 17α-methyltestosterone as a component of hormone replacement therapy.
17 alpha-methyl testosterone can be used as a functional androgen and endogenous estrogen production of oral active steroid inhibitors, but also for the prevention and treatment of hormone-sensitive cancer to provide special possibilities.
|Description||White or light yellowish crystalline powder||white powder|
|Loss On Drying||1.0%max||0.18%|
|Heavy Metals||10PPm max||<10PPm|
|Residue On Ignition||0.1%max||0.05%|
|Conclusion||The specification conform with enterprize standard|
Dose and management
When performing a methyl 1 test, it is best to start at least one week at a dose of 5-10 mg to understand your reaction. Many people have found that lower doses are equally effective with higher doses but with fewer side effects. Most people seem to find their ideal dose in the range of 10-30 mg. The length of the cycle should be kept short, in the range of 1-4 weeks.
Warning: M1T hormones can have side effects due to their extreme strength. We recommend using at least one good milk thistle supplement or cycle support (OCS) product with M1T Pro hormone to help protect your liver. We also recommend the use of good PCT immediately after any vigorous hormone therapy.
Those who are still seeking to use methylated reagents may be necessary to do so and will not accumulate with another synthetic metabolic / androgen steroid. For such use, it will be desirable to take 40-50 mg at a single daily dose for up to 8 weeks while waking up. Some people may wish to use this steroid, such as Dianabol, to start a cycle, and at the end of the longer injectable testosterone begins to get the results earlier, possibly with another basic compound, such as black ketone or norbornone. In that case again, taking the first 5-6 weeks of the cycle at about 30 mg in the single morning dose will provide the desired benefit.
Since this is only used for expansion stacks with fragile steroids, the severity of side effects will be severe. Need to verify that he first had no risk of hair loss or prostatic hypertrophy and had
adjuvant drugs such as Nolvadex, arimidex and finasteride to control side effects.
In terms of accessibility, if male breast development symptoms occur, you should start using 20mg of Nolvadex every day and start a cycle of 0.5mg anafenazole (arimidex). After 3-4 days, Nolva can be discontinued, but anastrozole should continue for some time. Some people ask me about using Proviron on this issue, but in my opinion, need to know how much DHT will use this compound to start, it may do more harm than good, add more it Proviron is 1- Methyl-DHT). Thus, anastrozole is quite expensive, but here is given priority. I usually disagree with the use of finasteride because DHT usually provides more benefits to the steroid user than the problem (except for those prone to hair loss), and its blocking may reduce the results obtained, in this case, especially in At the beginning of the longer injectable testosterone cycle, you can choose to study its use.
Testosterone is a hormone that is produced predominantly in male testes. It is responsible for almost all sexual men. This specific version is attached to testosterone with phenylpropionate.
17 alpha-methyl-1-testosterone has an active life of 4-5 days. Release time, it is directly in the middle of propionic acid (short) and Cypionate (long) version of testosterone. It is recommended to inject testosterone phenylpropionate testosterone twice a week, although many people like every three days.
How it works?
There are many possible side effects associated with the use of testosterone phenylpropionate. The product also has a high level of aromatization of estrogen and DHT (dihydrotestosterone) covering. Converted to estrogen, female sex hormones, resulting in male breast development (male breast tissue formation) and high risk of water retention.
Replenishing testosterone into your body will result in the closure of the body's natural production of hormones. The severity of side effects is largely determined by the dose and duration of circulating free testosterone and its transformation to the substrate. The metabolic / androgenic effects of testosterone depend on the dose, so the higher the dose, the higher the muscle establishment effect. Testosterone also promotes active and dominant behavior.
Testosterone may be the best known mass builder of human beings and is recommended as the basis for any large-scale construction cycle.
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