Dehydroisoandrosterone DHEA Muscle Gaining 99% Purity Strong Effect 53-43-0

Basic Information
Place of Origin: CHINA
Brand Name: TINGYI
Certification: GMP , ISO 9001:2008
Model Number: 53-43-0
Minimum Order Quantity: 10g
Price: Contact Me
Packaging Details: Disguised Package
Delivery Time: 2 Working Days
Payment Terms: Bank Transfer - Bitcoin - Western Union - MoneyGram
Supply Ability: 100 KG/Month
Product Name: DHEA CAS: 53-43-0
Appearance: White Powder Usage: Muscle Gaining
Shipping Method: EMS, HKEMS, FEDEX, DHL, UPS, Aramex, ETC Synonym: Dehydroisoandrosterone
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 Quick Detail


Product name Dehydroepiandrosterone
Other name DHEA
CAS No. 53-43-0
EINECS 200-175-5
MF C19H28O2
MW 288.4244
Molecular Structure Dehydroisoandrosterone DHEA Muscle Gaining 99% Purity Strong Effect 53-43-0 0
Appearance white or almost white crystalline powder, odorless
Testing method HPLC
Assay 99%
Certificate ISO9001
Shelf time 3 years

Dehydroisoandrosterone DHEA Muscle Gaining 99% Purity Strong Effect 53-43-0 1




Test Items Specification Test Results
Description White to almost white crystalline powder Conform
Melting point 166~170ºC 167-169°
Assay ≥98.0% 99.05%
Impurity ≤0.5% 0.13%
Loss on drying ≤0.5% 0.20%
Conclusion The above test result complied with standard




What is Dehydroepiandrosterone (DHEA)?


        Dehydroepiandrosterone (DHEA) is a precursor hormone, which means it has little biological effect on its own, but has powerful effects when converted into other hormones such as estradiol. Dehydroepiandrosterone is produced from cholesterol mainly by the outer layer of the adrenal glands, known as the adrenal cortex, although it is also made by the testes and ovaries in small amounts. It circulates in the blood, mainly attached to sulphur as dehydroepiandrosterone sulphate, which prevents the hormone being broken down. In women, dehydroepiandrosterone is an important source of oestrogens in the body – it provides about 75% of oestrogens before the menopause, and 100% of oestrogens in the body after menopause.





        Epiandrosterone can be used as an intermediate for steroids and contraceptives by 17β-hydroxy steroid dehydrogenase or through the 3β-hydroxy steroid dehydrogenase from male and maladione to natural steroids and androstenediol, Allowing the user to lift heavier and harder, it binds fat and burns directly, even suppressing aromatase, burning more body fat while reducing the risk of stopping from elevated estrogen. Moreover, Epiandrosterone inhibits SHBG, resulting in a slight increase in circulating estrogen and free testosterone levels. Corticosterone is used to accelerate fat loss, increased strength, lean body weight gain, increased muscle hardness, improved sexual desire.





        Dehydroepiandrosterone (DHEA) is a natural hormone produced by the adrenal gland, and many bodybuilders are using DHEA to gain a competitive advantage. Recent studies have now shown that supplements enhance lean muscle mass and minimize body fat and compare with natural steroids.

        DHEA is used to slow down or reverse aging, improve the thinking ability of the elderly, slow down the progress of Alzheimer's disease. Athletes and others use DHEA to increase muscle mass, strength and energy. But DHEA's use is prohibited by the National University Sports Association (NCAA). DHEA is also used by men for erectile dysfunction (ED), as well as healthy women and women who have low levels of certain hormones to improve health and sex behavior.






Prevent obesity:

        Androstenolone has a thyroid effect, and it could inhibit food and fat intake, reducing fat accumulation. Oral small doses of DHEA sulfate have a certain role of improving the amount and distribution of body fat and lipid-lowering. In addition, DS could act on mitochondrial respirators and inhibit food and fat intake. It is also related to DHEA against glucocorticoid, preventing obesity.



        DHEA has an effect of improving glucose tolerance and insulin levels, and it is anti-diabetic.


Anti-cortical disease:

         Androstenolone could enhance activity of endocrine system, and reduce cortisol levels. It is also resistant to a variety of pathological processes. The symptoms have greatly improved after taking Androstenolone of systemic lupus erythematosus (SLE) patients, indicating that Androstenolone works on SLE disease. DHEA helps body get cortical antibodies. Androstenolone concentration in plasma is greatly related to variety of cortical diseases: the lower the concentration, the greater the risk of illness.


Effect on sclerotin:

        Prasterone itself can not affect the growth and differentiation of human osteoblasts directly, but can affect the growth and differentiation of osteoblasts by affecting the changes of 1, 25-dihydroxyvitamin D3. The effect of DHEA on sclerotin depends on the form of existence of sex hormones in osteocytes and their endocrine effects on osteoblasts.


Protein metabolism:

        DHEA is a protein that assimilates hormones and has the effect of promoting protein synthesis. According to Marrero and other studies, feeding mice with prasterone (0.45%) could increase their liver weight, and increase liver mitochondria by induced liver protein, so restoring RNA and protein synthesis.



       Extensive clinical research of prasterone has been made on the treatment of menopausal syndrome, scleroderma, coronary heart disease, gout, psoriasis, AIDS and so on. The study also found that the pathogenesis of tuberculosis cytoplasm deformation is associated with concentration of adrenal cortex hormones and anti-adrenocorticotropic hormones; fetal plasma cortisol (Cortisol)/DHEA-S concentration has a great relationship with childbirth.



        Orally administered DHEA has a less than 10% bioavailability and is converted into inactive DHEAS, which can then act as a reservoir for the body to utilize. Daily dosing of DHEA 25 mg has been suggested in postmenopausal women because this dose minimizes the adverse androgenic effects; however, only studies in which at least 50 mg/day were used demonstrated positive outcomes.

        Dosages used in clinical studies of assisted reproduction were in the range of 50 to 75 mg/day (in divided doses). In adrenal insufficiency, DHEA 50 mg/day for 3 months is considered a replacement dose, while 200 mg/day achieves supraphysiological circulating levels and would thus be considered a pharmacological dose.

Dehydroisoandrosterone DHEA Muscle Gaining 99% Purity Strong Effect 53-43-0 2

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