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Home>Products>Legal Anabolic Steroids>White Halotestin Fluoxymesterone Powder Anti Breast Cancer CAS 76-43-7
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White Halotestin Fluoxymesterone Powder Anti Breast Cancer CAS 76-43-7
- LSW
76-43-7
- China
- GMP, ISO9001, USP, KOSHER
- 10g
- Negotiable
- Discreet disguised package or as required
- 3-7 working days
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- 5000kg/week
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Wuhan Liantian Technology Co.,Ltd2020-07-10 09:46:19
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Product Details
| CAS No.: | 76-43-7 | MF: | C20H29FO3 | MW: | 336.44 |
| Appearance: | Powder | Purity: | 99% | Usage: | Bodybuilding |
Product Description
Unfortunately for bodybuilders, its muscle-building attributes are not as effective. Halotestin doesn convert to estrogen in the body, but it is toxic to the liver, so small doses are recommended.
Structurally Halotestin is a derivative of testosterone, differing from our base androgen by three structural alterations (specifically l7alpha-methyl, 11 beta-hydroxy and 9-fluoro group additions). The result is a potent oral steroid that exhibits extremely strong androgenic properties. This has a lot to due with the fact that it is derived from testosterone, and as such shares important similarities to this hormone. Most importantly, like testosterone, Halotestin appears to be a good substrate for the 5-alpha reductase enzyme. This is evidenced by the fact that a large number of its metabolites are found to be 5-alpha reduced androgens, which coupled with its outward androgenic nature, suggests it is converting to a much more active steroid in androgen responsive target tissues such as the skin, scalp and prostate.
| Product name | Halotestin | |
| Appearance | White crystalline powder | |
| Identification | A. B. | Positive |
| Assay | 97.0~102.0% | 98.60% |
| Specific Rotation | +104°~+112° | +107.8° |
| Loss On Drying | 1.0%max | 0.35% |
| Chromatographic Purity | Single impurity: 1.0%max | <1.0% |
| Total impurities: 2.0%max | <2.0% | |
| Organic Volatile Impurities | Meets the requirement. | Conforms |
Dosage:
The dosage will vary depending upon the individual, the condition being treated, and its severity. The total daily oral dose may be administered singly or in divided (three or four) doses.
Male hypogonadism: For complete replacement in the hypogonadal male, a daily dose of 5 to 20 mg will suffice in the majority of patients. It is usually preferable to begin treatment with full therapeutic doses which are later adjusted to individual requirements. Priapism is indicative of excessive dosage and is indication for temporary withdrawal of the drug.
Delayed puberty: Dosage should be carefully titrated utilizing a low dose, appropriate skeletal monitoring, and by limiting the duration of therapy to four to six months.
Inoperable carcinoma of the breast in the female: The recommended total daily dose for palliative therapy in advanced inoperable carcinoma of the breast is 10 to 40 mg. Because of its short action, fluoxymesterone should be administered to patients in divided, rather than single, daily doses to ensure more stable blood levels. In general, it appears necessary to continue therapy for at least one month for a satisfactory subjective response, and for two to three months for an objective response.
Side Effects:
Endocrine and urogenital
Female: the most common side effects of androgen therapy are amenorrhea and other menstrual irregularities; inhibition of gonadotropin secretion; and virilization, including deepening of the voice and clitoral enlargement. The latter usually is not reversible after androgens are discontinued. When administered to a pregnant woman, androgens can cause virilization of external genitalia of the female fetus.
Male: Gynecomastia, and excessive frequency and duration of penile erections. Oligospermia may occur at high dosage.
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