Dihydrotestosterone can be produced directly by the testicles, or it can be converted from the surrounding tissues by androgens and estrogens as precursor substances. It can promote the normal development of external genitalia and prostate, has a positive effect on the emergence and maintenance of secondary sexual characteristics, and promotes the maturation of sperm in the epididymis Chemicalbook. Clinically, it is mainly used for differential diagnosis of benign prostate diseases caused by sexual differentiation abnormalities caused by 5α-reductase defects. It is also of great significance to observe the curative effect of prostate tumor, sexual dysfunction, infertility, female hirsutism and so on.
It is used for negative nitrogen balance caused by chronic wasting diseases, osteoporosis, serious infections and trauma burns, etc., to promote the growth of premature and immature infants. Fracture is not easy to heal, hypercholesterolemia, postpartum weakness can also be used
E tele a matou fale gaosi oloa maualuga ma le galulue faʻatasi, lea e mafai ona tuʻuina atu ia te oe oloa maualuga ma tau faʻatauvaʻa. Ma e mafai foi ona matou tuʻuina atu faʻaitiitiga mo faʻatauga tele.Ma matou te galulue faʻatasi ma le tele o kamupani faʻapolofesa felauaiga uta, e mafai ona tuʻuina atu oloa ma le saogalemu ma le sologa lelei i ou lima. Le taimi tu'uina atu e tusa ma le 3-20 aso talu ona fa'amaonia le totogiina.
Product Name: | Stanolone |
Synonyms: | (5S,8R,9S,10S,13S,14S,17S)-17-Hydroxy-10,13-dimethyltetradecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one;5α-androstan-17β-ol-3-one solution,100ppm;(8R,9S,10S,13S,14S)-17-hydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one;(5-alpha,17-beta)-17-hydroxyandrostan-3-one;(5alpha,17beta)-17-Hydroxy-androstan-3-one;17beta-Hydroxy-3-androstanone;17-beta-hydroxy-5-alpha-androstan-3-on;17-hydroxy-,(5-alpha,17-beta)-androstan-3-on |
CAS: | 521-18-6 |
MF: | C19H30O2 |
MW: | 290.45 |
EINECS: | 208-307-3 |
Product Categories: | API |
Mol File: | 521-18-6.mol |
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Stanolone Chemical Properties |
Liu liusuavai | 178-183 °C |
alpha | 27 º |
Fa'apuna | 372.52°C (rough estimate) |
mafiafia | 1.0320 (rough estimate) |
fa'asino fa'asino | 1.4709 (estimate) |
Fp | 9℃ |
vevela vevela. | 2-8°C |
solubility | Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml |
pka | 15.08±0.60(Predicted) |
Suavai Solubility | 344.3g/L(temperature not stated) |
Merck | 13,8872 |
BRN | 2056371 |
InChIKey | NVKAWKQGWWIWPM-ABEVXSGRSA-N |
CAS DataBase Reference | 521-18-6(CAS DataBase Reference) |
NIST Chemistry Reference | Stanolone(521-18-6) |
EPA Substance Registry System | Androstan-3-one, 17-hydroxy-, (5.alpha.,17.beta.)- (521-18-6) |
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