ProName: Oxandrolone
CasNo: 53-39-4
Molecular Formula: C19H30O3
Appearance: white crystalline powder
Application: medical intermediate
DeliveryTime: within a week
PackAge: A variety of packing ways for your choice
Port: China
ProductionCapacity: 200 Kilogram/Month
Purity: 98.5%
Storage: Kept in a well-closed, light-resistant,dry and cool place
Transportation: EMS, HKEMS, DHL, TNT, UPS, Fedex
LimitNum: 10 Gram
Moisture Content: 0%
Impurity: 0.05%
Water content: 0%
Anavar was the old U.S. brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer Searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children.
One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men.
Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis.
As the opinions surrounding steroids began to change in the 1980′s, prescriptions for oxandrolone began to drop. Lagging sales probably led Searle to discontinue manufacture in 1989, and it had vanished from U.S. pharmacies until recently. Oxandrolone tablets are again available inside the U.S. by BTG, bearing the new brand name Oxandrin. BTG purchased rights to the drug from Searle and it is now manufactured for the new purpose of treating HIV/AIDS related wasting syndrome.
Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (DHT).
Oxandrolone is widely used due to its exceptionally small level of androgenicity[citation needed] accompanied by moderate anabolic effect. Although oxandrolone is a 17-alpha alkylated steroid, its liver toxicity is very small as well
In the past decades, it was used to treat individuals with a variety of anemias, weight loss in HIV patients and was once tried out as treatment for osteoporosis. Today, some physicians do prescribe Oxandrolone to treat moribund patients gain weight after trauma, burns or serious infections. The drug is also used to offset protein catabolism due to prolonged usage of corticosteroids and for the relief of bone pain caused by osteoporosis.
Oxandrolone is both an anabolic steroid and has all the properties of an androgenic drug. The actions of the Oxandrolone is similar to testosterone. But Anavar is often called a weak testosterone. It has two advantages compared to other steroids. Firstly, it does not converted into estrogen and it does not significantly influence the hypothalamic pituitary tract at low doses. What this means is that because it is not broken down to estrogen, males will not develop breast enlargement Secondly, because it does not affect the hypothual pituitary axis. It dose not affect the suppression of testosterone. This means that the individual taking Anavar will not have such side effects like loss of libido, impotence or testicular atrophy- features that are commonly seen with other anabolic steroids
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 20-50mg 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.
Clinically, this drug is used to treat body wasting diseases and bone pains caused by osteoporosis, muscle gains. Anavar is referred to as a mild anabolic androgenic steroid since it exhibits great results with slight side effects.
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