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Drostanolone enanthate is an artificially synthesized steroid compound formed by the combination of drostanolone and enanthate. The Molecular formula is C27H44O3, CAS 13425-31-5, and its molecular weight is about 416.64g/mole. It is a white crystalline solid. The specific optical rotation is usually between+34 degrees and+39 degrees. Relatively stable at room temperature, but gradually decomposes under high temperature, humidity, and light conditions. It is relatively stable to acids and bases, but prolonged exposure to strong alkaline or acidic environments may lead to degradation. It can stimulate Erythropoiesis and has therapeutic effect on anemia patients caused by some diseases. Other uses outside the chemical field, including stimulants, non medical cosmetic and sports enhancement, are strictly prohibited.

|
Chemical Formula |
C27H44O3 |
|
Exact Mass |
416 |
|
Molecular Weight |
417 |
|
m/z |
416 (100.0%), 417 (29.2%), 418 (2.7%), 418 (1.4%) |
|
Elemental Analysis |
C, 77.84; H, 10.65; O, 11.52 |


A common method for synthesizing Drostanolone enanthate in the laboratory is as follows:
Step 1: Preparation of 2-Bromo-4,6-difluorobenzene
-Starting from 2,4-Difluorobenzoic acid, 2-bromo-4,6-difluorobenzoic acid was obtained through a series of chemical reactions.
Step 2: Prepare 3-hydroxy-2-aminopropionic acid ethyl ester
-The acetone Magnesium bromide is reacted with Ethyl acetoacetate to obtain 3-hydroxy-2- Pyruvic acid ethyl ester, and then 3-hydroxy-2-amino Ethyl propionate is prepared through reduction, acidification and other reactions.
Step 3: Preparation of Drostanolone
-Drostanolone was obtained by Condensation reaction of 2-bromo-4,6-difluorobenzoic acid and 3-hydroxy-2-aminoethyl Ethyl propionate in alkaline condition.
Step 4: Preparation of product
-The reaction of Drostanolone with Enantic anhydride in the presence of an acid catalyst yields product.
The Chemical equation is simplified as follows:
Step 1:
C7H4F2O2+PBr3 → C7H3BrF2O2
Step 2:
C4H10BrMgN+C6H10O3 → 3-Hydroxy-2-acetylpropionic acid ethyl ester
3-Hydroxy-2-acetylpropionic acid ethyl ester+LiAlH4 → C4H9NO3
Step 3:
C7H3BrF2O2+C4H9NO3 → C20H32O2
Step 4:
C20H32O2+C14H26O3 → C27H44O3

It is a synthetic androgen compound that belongs to the category of artificially synthesized steroid compounds. In addition to the methods mentioned above, there is another common method for synthesizing product in the laboratory.
The synthesis method in this laboratory is mainly divided into the following steps:
Step 1: Preparation of 3-chloro-17-hydroxy-5- β- Sterene
-Starting from sitosterol, 3-chloro-17-hydroxy-5 is obtained through multiple reactions- β- Sterene.
Step 2: Preparation of 3-bromo-17-hydroxy-5- β- Sterene
-Add 3-chloro-17-hydroxy-5- β- Sterene reacts with bromine gas to obtain 3-bromo-17-hydroxy-5- β- Sterene.
Step 3: Prepare Drostanolone
-Add 3-bromo-17-hydroxy-5- β- The sterone and acetone undergo Condensation reaction to produce Drostanolone.
Step 4: Prepare product
-The reaction of Drostanolone with Enantic anhydride in the presence of an acid catalyst yields product.
The Chemical equation is simplified as follows:
Step 1:
C29H50O → 3-Chloro-17-hydroxy-5- β- STERENE
Step 2:
3-Chloro-17-hydroxy-5- β- Sterene+Br2 → 3-Bromo-17-hydroxy-5- β- STERENE
Step 3:
3-Bromo-17-hydroxy-5- β- STERENE+C3H6O → C20H32O2
Step 4:
C20H32O2+C14H26O3 → C27H44O3
It should be noted that this is just another synthesis method for product, and the specific experimental conditions, reaction temperature, catalysts, and other details may vary depending on different laboratories or researchers. For practical operations, please follow the relevant chemical experimental procedures and conduct them in a safe environment. At the same time, steroid substances have potential abuse and harm, please comply with relevant laws and regulations as well as medical ethical requirements.

Drostanolone enanthate is a synthetic androgen substance commonly used in the fields of medicine and sports.
1. Medical applications:
-Breast cancer treatment: It is used in the treatment of breast cancer. It works by inhibiting the estrogen receptor in breast cells, thereby reducing the growth of breast cancer cells.
-Osteoporosis treatment: Due to the androgenic properties of Drostanolone, it can increase bone density and be used to treat osteoporosis.
-Increase Erythropoiesis: It can also stimulate Erythropoiesis, which has therapeutic effect on anemia patients caused by some diseases.
2. Exercise enhancement:
-Enhancing muscle growth: It is used as a drug to enhance muscle growth and strength. It can promote protein synthesis, improve nitrogen balance, and increase muscle mass and weight.
-Improve sports performance: Since Drostanolone enhate has the function of enhancing Erythropoiesis, it can provide more oxygen to the muscles, thus increasing endurance and sports performance.

3. Beauty applications:
-Reduce fat accumulation: It is used to reduce the accumulation of fat in the body. It can promote the breakdown and metabolism of fat, helping people shape a slimmer body shape.
-Increase skin firmness: Drostanolone enanthate can increase collagen synthesis, improve skin elasticity, and reduce wrinkles and sagging.
-Improve collagen synthesis: Collagen is the main structural protein of the skin, and steroids may stimulate collagen synthesis, thereby improving skin elasticity, reducing wrinkles and relaxation.
Precautions for steroid use:
-Consulting professionals: If you are interested in the use of steroids, it is recommended to consult a professional doctor, dermatologist, or beauty expert. They can provide suggestions based on your personal situation.
-Compliance with laws and regulations: Before using steroids, it is important to understand and follow local laws and regulations, and comply with medical ethics and professional ethics requirements.
-Potential risks: Steroids may cause a series of serious side effects and health problems, including but not limited to hormone imbalance, skin changes, blood circulation problems, etc. Therefore, any decision to use steroids should be based on sufficient understanding and careful consideration.
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