Anabolic Steroids, Oxanabol Anavar
|FOB Price:||US $9 / grams|
|Min. Order:||1 grams|
|Min. Order||FOB Price|
|1 grams||US $9/ grams|
|Transport Package:||1kg/Foil Bag|
|Payment Terms:||T/T, Western Union, Paypal, Money Gram, Bitcoin|
- Model NO.: 98
- Customized: Non-Customized
- Suitable for: Adult
- Purity: >98%
- Molecular Formula: C19h30o3
- Appearance: White Crystalline Powder
- Packing: Foil Bag
- Specification: 99
- HS Code: 3001200090
- Powder: Yes
- Certification: GMP, ISO 9001, USP, BP
- State: Solid
- CAS No.: 53-39-4
- Molecular Weight: 306.44
- Assay: 98%
- Trademark: moli
- Origin: China
Trade names: Anvar-10,Oxanabol,Glonavar
Appearance: white crystalline powder
Molecular Weight: 306.4442
Einecs No: 200-172-9
Melting Point: 235 238 Celsius
Effective dose: (Men) 20-100mgs/day - (Women) 2.5-20mgs/day
Active Life: 8-12 hours
Detection Time: 3 weeks
Anabolic/Androgenic Ratio (Range): 322-630:24
Usage: A synthetic, anabolic steroid. Used to promote muscle growth and combat involuntary weight loss. It has also been used to treat cases of osteoporosis.
|Description||White or Almost White Crystalline Powder||white crystalloid powder|
|Specific Rotation||-18C ~ -24C||-22.0C|
|Loss On Drying||1.0%max||0.13%|
|Organic Volatile Impurities||meets the requirements||Conforms|
|Residual Solvents||meets the requirements||Conforms|
|Residue On Ignition||0.2%max||0.05%|
|Conclusion||The specification conform with USP30 standard|
Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity has much to due 4vith the fact that it is a derivative of . Although you might think at first glance this would make it a more androgenic steroid, it in fact creates a steroid that is less androgenic because it is already "5-alpha reduced". In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent "dihydro° form. It is a simply matter of where a steroid is capable of being potentiated in the body, and with, Oxanabol we do not have the same potential as testosterone, which is several times more active in androgen responsive tissues compared to muscle tissue due to its conversion to DHT. It essence has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances.
This steroid is known as a good agent for the promotion of strength and duality muscle mass gains, although the mild nature of this compound makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 15-25mg (6-10 tablets) per day, a level that should produce noticeable results. It can be further combined with anabolics like Primobolan® and Winstrol® to elicit a harder. more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin®, Proviron® or trenbolone. In this case the androgen really helps to harden up the muscles, while at the same time making conditions more favorable for fat reduction. Some athletes do choose to incorporate oxanabol into bulking stacks. but usually with standard bulking drugs like testosterone or Dianabol.
The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol®, Primobolan® or Durabolin®. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup.
Studies using low dosages of this compound note minimal interferences with natural testosterone production. Likewise when it is used alone in small amounts there is typically no need for ancillary drugs like Clomid®/Nolvadex® or NCG. This has a lot to do with the fact that it does not convert to estrogen, which we know has an extremely profound effect on endogenous hormone production. Without estrogen to trigger negative feedback, we seem to note a higher threshold before inhibition is noted. But at higher dosages of course, a suppression of natural testosterone levels will still occur with this drug as with any anabolic/androgenic steroid.
This makes clear that while estrogen is important in this regard, androgen action triggers feedback inhibition as well. In the context of the average bodybuilder using this steroid at a level to promote growth, we would probably expect that maintaining a normal level of endogenous testosterone release would likewise be very difficult.
Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that is noted for putting stress on the liver. It is importar7t to point out however that to spite this alteration is generally very well tolerated, While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not a statistical problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. 20mg of in fact produced 72% less BSP retention than an equal dosage of fluoxyrnesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during loner cycles than most of other orals with this distinction. Although this may very well be true, the chance of liver damage still cannot be excluded.
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