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|Purity:||99%||Appearance:||White Crystalline Powder|
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Relief of Bone Pain Caused by Osteoporosis Anavar Orla Anabolic Androgenic Steroids Oxandrolone for Mucle Gaining White Powder
Anavar History and Overview:
Anavar is the trade name for the oral anabolic steroid Oxandrolone, which is the generic chemical name. Anavar was developed and marketed during the height of anabolic steroid research between the 1950s and the 1980s. It is the apex of the never-ending quest to discover and develop an anabolic steroid that could be considered perfect. With this being said, Anavar is perhaps the closest that science has come to developing what would be considered the perfect anabolic steroid. It is renowned for its remarkable safety profile and side effect-to-benefit ratio - so much so that it is one of the few anabolic steroids deemed suitable as a medication for females and children (two patient types that are known for responding quite negatively to anabolic steroid therapies to begin with).
Anavar’s history begins in 1962 as Oxandrolone. Not long afterwards, it was released onto the prescription medication market under the trade name Anavar by G.D. Searle & Co. Laboratories, which is today known as Pfizer Inc. Other trade and brand names have been utilized for Oxandrolone by other pharmaceutical companies. These names include: Protivar, Anatrophil, Antitriol, Lipidex, and Lonavar. Anavar was one of the pharmaceutical industry’s biggest successes on the prescription market due to the plethora of medical reports indicating a vast amount of patients that tolerated the drug quite well.
This medication is used to help people regain weight they have lost due to certain medical conditions (such as surgery, chronic infection, trauma, long term use of corticosteroid medication such as hydrocortisone/prednisone). It is also used to relieve bone pain due to bone loss (osteoporosis). Oxandrolone belongs to a class of drugs known as anabolic steroids. These drugs are similar to male hormones made by the body.
Oxandrolone is an orally ingested anabolic steroid that is normally prescribed in the 5-10mg per day range with prescribed doses rarely surpassing 20mg per day. Use will normally last 2-4 weeks followed by a short break and repeating the cycle until the issue is resolved. Use of this nature may in some cases last indefinitely.
For the male anabolic steroid user, 20-30mg per day although a low dose will produce an anabolic bump. However, 40-50mg per day is far more common and effective. Some men will use as much as 80-100mg per day, but keep in mind this does increase the chance of side effects.
Female Oxandrolone users will normally dose the steroid at 5-10mg per day. It’s not common for a woman to need more than 10mg per day, but if more is needed it can be increased by 5mg. Doses that surpass 20mg per day will almost assure some level of virilization. 6-8 weeks of use is standard with both men and women.
Chemical Name: 5alpha-androstan-2-oxa-17alpha-methyl-17beta-ol-3-one
Assay: 99% min.
Molecular Formula: C19H30O3
Molecular weight: 306.4
Packing: foil bag or tin.
Delivery: Express courier.
Character: White crystalline powder.
Categories: Miscellaneous; Biochemistry; Steroids (Others)
Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.
Anavar , unlike most oral compounds is categorized as a Class I anabolic steroid, most efficiently stacked with Class II compounds such as Dianabol or Anadrol.
Anavar adds little if anything to high-dose use of Class I anabolic steroids such as or to high-dose , which is classified as having mixed activity. It can be an aid, albeit an expensive one, to moderate dose testosterone usage.
Today, some physicians do prescribe Anavar 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.
Anavar is both an anabolic steroid and has all the properties of an androgenic drug. The actions of the Anavar is similar to testosterone base. 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
Anavar has often been called a weak steroid. Part of the reason for this is that use of a Class I steroid alone never is maximally effective. The other cause is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids.
Anavar has given optimistic consequences in taking care of anemia and hereditary angioedema. Proven studies though have given links linking expanded use of the medicine and problems of liver toxicity like to those found with additional 17α-alkylated steroids. Yet in little dosages, numerous patients shown gastro-intestinal troubles such as bloating, nausea, and diarrhea.
Anavar's specificity targeting the androgen receptor predestined that, unlike lot other steroids, it had not been seen to give stunted development in teens people, as well at usual measure not often observed clear masculinising reactions external of stimulating strength growth.
Anavar does not aromatize at any measure, and is not without problems ingested into DHT or estrogen. As such, a typical dose of 20-30 mg offered eminent androgen levels for up to eight hours. To enlarge use, bodybuilders classical "stacked" the Anavar with others such as , advance enhancing corp power increase.
Anavar,also called Lonavar,Oxandrin,Vasorome, its chemical name is 17beta-Hydroxy-17-methyl-2-oxa-5alpha-androstan-3-one. It is a kind of oral testosterone drugs synthetised by actively metabolizing anabolic. It researched that 20mg daily dose has an effect on weight gaining and rehabilitation muscle for who encounters large area burnt.
Anavar,which comes out of androgenic character, can cause retention of nitrogen, potassium and phosphorus, and promote anabolism and inhibit excessive catabolism. It is widely used for boys who come across abnormal growth and late puberty, and also girls who encounter congenital ovarian hypoplasia.
Anavar absorbed rapidly according to intestines and stomach. Its metabolites and unchanged excreted by the kidneys, and small amount exclude from gastrointestine.
|Description||: White or Almost White Crystalline Powder||white crystalloid powder|
|Specific Rotation||: -18° ~ -24°||-22.0°|
|Loss On Drying||: 1.0%max||0.13%|
|Organic Volatile Impurities||: meets the requirements||Conforms|
|Ordinary Impurities||: 2.0%max||<2.0%|
|Residual Solvents||: meets the requirements||Conforms|
|Residue On Ignition||: 0.2%max||0.05%|
|Conclusion||The specification conform with USP30 standard|
Anavar recipe injection :
1)Highest concentration made -50ml @ 20mg/ml 1 gram of powder
9.8 ml's of PEG 300
39.2 ml's of 190 Proof Grain Alcohol
2)50ml @ 50mg/ml
2.5 grams Anavar (2.5ml) 2.5ml BA
2.5ml BB 5ml guaiacol 37.5ml Oil
Anavar / Oxandrolone Half Life
Anavar does not aromatize or convert to DHT, and has an 8 hour half-life. Thus, a moderate dose taken in the morning is largely out of the system by night, yet supplies reasonable levels of androgen during the day and early evening.
One study found oxandrolone to be superior to testosterone and to Deca (nandrolone) for reducing abdominal fat in men, or at least in obese older men at the specific low doses studied, which were not necessarily equipotent. From this, some have made broad generalizations to bodybuilding. However, this does not necessarily carry over to anabolic steroid cycles at doses commonly used in bodybuilding. In the case of the study in question, I expect the difference in outcomes was dose-related.
In practice, at total androgen doses typically used, one can cut just as effectively without oxandrolone as with, given any of various possible substitutions for the oxandrolone. This is not to say this drug is ineffective, but rather that other androgens including testosterone are also effective at high dose for abdominal fat loss.
In the case of low-dose use however, I do think it is a correct conclusion that for most, low dose Anavar use is more effective for cutting than equal dosages of most other anabolic steroids. This may be partly or entirely from additive effect with natural testosterone: such oxandrolone use may not suppress such its production, the user may enjoy both the full effect of his natural testosterone and the effect of the oxandrolone. In contrast, low-dose testosterone or nandrolone use results in substantial suppression of natural testosterone, and so there is less total effect.
Oxandrolone, as with other 17-alkylated steroids, is hepatotoxic. At one time it was thought that it is not, but both clinical and practical experience with Oxandrin has shown that liver toxicity can indeed be an issue with prolonged use. I believe the usual principle of limiting 17-alkylated use to 6 weeks at a time should be applied when oxandrolone is used, just as with any alkylated oral.
Trenbolone or Primobolan are suitable substitutes for Anavar, without the liver toxicity issues. As a substitute, Primobolan shares the property of being low-suppressive, while trenbolone does not.
An interesting application of the drug that takes advantage of its oral administration is use as a morning-only bridging agent between cycles, which in my opinion should be done - if done - only after fully recovering normal testosterone production from the last cycle. At least 20 mg is usually acceptable in this application. Ideally, testosterone levels will be measured to monitor such bridging. A factor limiting to such bridging is the liver toxicity issue.
With regard to use by women, while there is a common belief that Anavar is minimally virilizing to female, in fact virilization is not unusual at 20 mg/day and can occur at considerably lower doses than that. Even 5 mg/day is not side-effect-free for all.
During a cycle, oxandrolone is not particularly recommended because there are more cost-efficient choices that will fully accomplish the same goals and do not add to liver toxicity.
The two best uses for Anavar are in optional bridging periods between cycles, if such are employed, while keeping care to avoid excessive duration of continuous 17-alkylated use; and, if short-acting injectables are not available, to supplement cycles as levels fall between the time of last injection and the start of post-cycle therapy so that that time period can remain effective for gains.
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