Product Details:
Payment & Shipping Terms:
|
| Product Name: | Andarine | Other Name: | S4 |
|---|---|---|---|
| CAS: | 401900-40-1 | Category: | SARMs |
| Appearance: | White Powder | Usage: | Weight Loss |
| High Light: | fat loss steroids,lose weight steroids |
||
Fat Loss Injections Steroids S4 Andarine SARMs Bodybuilding 401900-40-1
| Product Name | Andarine |
|
Synonym |
GTx-007, S4 |
| CAS | 401900-40-1 |
| Assay | 99% |
| Packing | 1kg net/foil bag, 5kg/drum. |
| Standard | Enterprise Standard |
| Storage | Shading , Confined Preservation |
| Usage | For treatment of conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy |
| Molecular Fomular | C19H18F3N3O6 |
| Molecular Weight | 441.36 |
| MolecularStructure |  |
Andarine S4 Application
S-4 is designed for treating conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy, using the non-steroidal androgen antagonist bicalutamide as a lead compound.
As an orally active partial agonist for androgen receptors, S-4 is effective in not only maintaining lean body mass but actually increasing it.
SARMS such as S4 can cause muscle growth in the same manner as steroids, however unlike testosterone
and other anabolic steroids, SARMS (as nonsteroidal agents) do not produce the growth effect on prostate and other secondary sexual organs.
The typical dose for cutting is 50 mg for a cycle of 6 to 8 weeks. The cycle should include using the product daily for 5 days and then taking 2 days off for the duration. Tasking the dose every day for the duration of the cycle can result in changes to vision.
Andarine S4 COA
| Test Item | Analysis Specification | Result |
| Description | Crystalline powder | Conforms |
| Melting range | 129°C~132°C | 130.8°C-131°C |
| Loss on drying | ≤0.5% | 0.20 % |
| Specific rotation | -58°~-62°(C=1,in CH3OH) | -61.05° |
| Sulphated ash | ≤0.1% | 0.08 % |
| Heavy metals | ≤10ppm | Conforms |
| Chlorides | ≤0.02% | Conforms |
| Sulfates | ≤0.02% | Conforms |
| Fluorine | 14.7%~17.9% | 15.2% |
Residual solvent |
Methanol ≤0.2% Isopropanol ≤0.2% Ethyl acetate≤0.2% Chloroform ≤0.2% |
0.0% 0.0% 0.0% 0.0% |
| Related substances (HPLC) |
Single impurity ≤0.2% Total impurities ≤0.5% |
0.05% 0.08% |
| Assay | ≥99.5% | 99.9% |
| Conclusion | Accordance with the reference | |
Andarine (S4) Introduction
Andarine, commonly known as S4, is a Selective Androgen Receptor Modulator (SARM) developed by GTx. Like all SARM's S4 was developed in the treatment of muscle wasting diseases with benign prostatic hypertrophy treatment also being high on the list of possible treatment benefits. Andarine is not as strong as some of the other SARM's in terms of an anabolic effect that leads to the promotion of lean muscle tissue increases, but it does appear to have other benefits that can prove to be highly valuable. Being an effective SARM, like most SARM's it is relatively side effect friendly with most users making it an increasingly common option for performance enhancing athletes.
Andarine (S4) Profile
Andarine (S4) was developed by GTX Inc. for the treatment of muscle wasting, osteoporosis and BPH (enlargement of the prostate). It belongs to the class of drugs called SARM's - selective androgen receptor modulators. Today, it is popularly used and sold as a research chemical, which is used by athletes who seek to get all of the strength benefits and lean muscle gains without the harmful side effects observed with anabolic steroids. Moreover, andarine is also used as part of steroid stacks to improve a cycle without adding more side effects, or aromatization.
S4 Andarine Review
Andarine (S4) is a solid SARM if the user understands its purpose. For gains in size it's not a good choice but for the cutting athlete or one looking to increase strength it is a viable and worthwhile consideration. However, due to the possible vision issues during use, this can make it one of the more unpleasant SARM's to use. How likely or how severe such issues may be is highly genetically dependent.
S4 really does give great progress. I have to say that I have lost a significant amount of weight while running Andarine as I'm burning more calories to build and repair muscle for those intense muscle gains.
How does it work?
Selective androgen receptor modulators (SARMS) bind to the androgen receptor and demonstrate osteo (bone) and myo (muscular) anabolic activity.
Binding and activation of the Androgen receptor alters the expression of genes and increases protein synthesis which ultimately builds muscle.
SARMS such as S4 can cause muscle growth in the same manner as steroids, however unlike testosterone and other anabolic steroids, SARMS (as nonsteroidal agents) do not produce the growth effect on prostate and other secondary sexual organs.
SARMS not only represent a new potential treatment option for a wide spectrum of conditions such as muscle wasting diseases (from age-related to AIDS or cancer-related), but they also have immense potential for muscle building for Bodybuilders, fitness and athletes.
S-4 in particular binds to the androgen receptor in muscle and bone to a third of the affinity of Testosterone.
Usage:
Andarine (GTx-007, S-4) is an investigational selective androgen receptor modulator (SARM) developed by GTX, Inc for treatment of conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy,[1] using the non-steroidal androgen antagonist bicalutamide as a lead compound.
Side effects:
S-4 is a little suppressive at high doses. Comparably, it is not as suppressive as LGD-4033, but it’s more than Ostarine. The recommendation is to follow its use with a post cycle therapy regimen immediately. Even though modified mini-pct is said to be excellent for recovery, using of supplements like HCGenerate is sufficient to address the little suppression caused.
It binds to the ocular receptors in the eye to create a faint yellow tint, which sometimes makes it difficult to adjust to darkness; though this is not prevalent among those experimenting with S-4, and it proves short-term as it goes away after discontinuing its use. It does not aromatize into estrogen; thus it requires no inhibitor on cycle.
