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Drostanolone

CAS No.
58-19-5
Chemical Name:
Drostanolone
Synonyms
Metholone;Medrotestron;DROSTANOLONE;Dromostanolone;58-19-5 Dromostanolone;Drostanolone/Dromostanolone;Dihydro-2α-Methyltestosterone;2α-Methyl-5α-dihydrotestosterone;2α-Methyl-5α-androstan-17β-ol-3-one;5α-ANDROSTAN-2α-METHYL-17β-OL-3-ONE
CBNumber:
CB1911442
Molecular Formula:
C20H32O2
Molecular Weight:
304.47
MDL Number:
MFCD00198322
MOL File:
58-19-5.mol
MSDS File:
SDS
Last updated:2023-11-01 16:49:00

Drostanolone Properties

Melting point 145-147°C
alpha D +32° (ethanol)
Boiling point 420.3±45.0 °C(Predicted)
Density 1.058±0.06 g/cm3(Predicted)
storage temp. Refrigerator
solubility Acetonitrile: 1 mg/mL; Ethanol: 1 mg/mL; Methanol: 1 mg/mL
form A crystalline solid
pka 15.09±0.70(Predicted)
CAS DataBase Reference 58-19-5
FDA UNII 7DR7H00HDT
NIST Chemistry Reference Drostanolone(58-19-5)

Drostanolone price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21170 Drostanolone ≥98% 58-19-5 1mg $32 2024-03-01 Buy
Cayman Chemical 21170 Drostanolone ≥98% 58-19-5 5mg $93 2024-03-01 Buy
American Custom Chemicals Corporation SHG0000431 DROSTANOLONE 95.00% 58-19-5 100MG $779.63 2021-12-16 Buy
American Custom Chemicals Corporation SHG0000431 DROSTANOLONE 95.00% 58-19-5 1G $2194.5 2021-12-16 Buy
Product number Packaging Price Buy
21170 1mg $32 Buy
21170 5mg $93 Buy
SHG0000431 100MG $779.63 Buy
SHG0000431 1G $2194.5 Buy

Drostanolone Chemical Properties,Uses,Production

Description

Drostanolone, also known as Dromostanolone[58-19-5], is an anabolic hormone and a derivative of methyltestosterone. Its action is similar to that of Conviron. Its anabolic effect is 4 times that of methyltestosterone and its androgenic activity is 0.39 times that of the latter. It is clinically used in the treatment of chronic wasting disease, pediatric underdevelopment, old age and frailty, serious illness and postoperative weakness, osteoporosis, aplastic anemia, leukopenia, thrombocytopenia, and hyperlipidemia.

Chemical Properties

White or off-white crystalline powder, odorless. Insoluble in water, slightly soluble in ethanol, slightly soluble in ether, soluble in chloroform.

Originator

Drolban,Lilly,US,1961

Uses

Drostanolone is a synthetic estrogen antagonist and is classified as an anabolic androgenic steroid. It has been used in sports to improve athletic performance and can be detected in urine. In the United States, Drostanolone is classified as a Schedule III substance, indicating it is regulated and controlled. This product is intended for research and forensic applications.

Definition

ChEBI: Metholone is a 17beta-hydroxy steroid, an anabolic androgenic steroid and a 3-oxo-5alpha-steroid. It has a role as an anabolic agent and an antineoplastic agent.

Manufacturing Process

A mixture of 1 gram of 2-hydroxymethylene-dihydrotestosterone, 10 cc of pyridine and 2 cc of propionic anhydride was allowed to react at room temperature for 16 hours and then poured into water. The resulting suspension was heated for 1 hour on the steam bath to hydrolyze the excess of propionic anhydride, cooled and extracted with methylene dichloride. The extract was consecutively washed with dilute hydrochloric acid, sodium bicarbonate solution and water, dried over anhydrous sodium sulfate and evaporated to dryness under vacuum. There was thus obtained the dipropionate of 2-hydroxymethylenedihydrotestosterone which was treated with hydrogen, in methanol solution.
When the uptake of hydrogen ceased, the catalyst was filtered and the solution was evaporated to dryness under vacuum. The residue was dissolved in a mixture of benzene-hexane, transferred to a chromatographic column with neutral alumina and the product was eluted with mixtures of benzenehexane, gradually increasing the proportion of benzene in the mixture. Crystallization of the eluates from acetone-hexane yielded the propionate of 2α-methyldihydrotestosterone(Dromostanolone).

brand name

Drolban (Lilly).

Therapeutic Function

Cancer chemotherapy

Synthesis

Drostanolone is prepared by this “one-pot-reaction”-step the conversion to the 1α-methyl-group is performed simultaneously with the cleavage of the protective group at the 17β-alcohol: 10.60 g Hydroxymethylene-precusor 2-Hydroxymethylene-androstan-17β-((tetrahydro-2H-pyran-2-yl)oxy)-3-one was nearly dissolved in 800 ml ethanol at 55°C. This solution was hydrogenated in a pressure vessel (Parr reactor) with 6.00 g palladium on charcoal (5%) at 4 bar and room temperature for 24 h. The mixture was filtered twice through paper and the corresponding ethanol solution was evaporated, to yield 9.50 g colorless oil, still contains traces of charcoal and ethanol. The crude product was purified by column chromatography on silica gel by using hexane-ethyl acetate (8:2) as an eluent, to afford 5.45 g purified Drostanolone as a colorless solid (69%) . MS (ESI+): m/z = 304.96 (calculated MW: 304.47 g/mol) Rf: 0.35, hexane/ethyl acetate 7:3, visualized by Seebach derivatization reagent. 1 H NMR(300 MHz, DMSO-d6) : δ 4.42 (d, 1 H, OH), 3.42 (m, 1H, HCHOH), 3.32 (s, 1H, CH), 2.37 (t, 1 H, CH), 1.99 (dd, 1 H, ), 1.84 (dd, 1H), 1.78 – 1.84 (m, 1H), 1.72 (m, 1H), 1.61 (m, 1H), 1.22-1.58 (m, 8H), 1.08 – 1.22 (m, 1H), 1.03 (s, 3H, CH3), 0.76-1.01 (m + d, 7H, 2α-CH3 +X), 0.65 – 0.72 (m, 1H), 0.64 (s, 3H, CH3).

Mode of action

It can promote protein synthesis and inhibit protein xenobiosis, reduce calcium and phosphorus excretion and alleviate bone marrow suppression, promote growth and development, promote tissue renewal and granulation, and reduce blood cholesterol, and have preventive and antagonistic effects on adrenocorticotropic hormone long-term use of adrenocorticotropic hypoplasia and protein anisotropy.

References

[1] SCH?NZER W, DONIKE M. Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites[J]. Analytica Chimica Acta, 1993, 275: 23-48. DOI:10.1016/0003-2670(93)80274-O.
[2] KINTZ P, GHEDDAR L. Evidence of use of drostanolone, an anabolic steroid, at the time the subject committed a murder: Place of hair analysis[J]. Toxicologie Analytique et Clinique, 2021. DOI:10.1016/J.TOXAC.2021.05.002.
[3] LIU Y, LU J, YANG S, et al. New drostanolone metabolites in human urine by liquid chromatography time-of-flight tandem mass spectrometry and their application for doping control[J]. Steroids, 2016, 108: 61-67. DOI:10.1016/j.steroids.2016.01.013.

Drostanolone Preparation Products And Raw materials

Drostanolone Suppliers

Global( 27)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23556 58
Hubei Harvest Chemical CO.,Ltd
+86-13129915771 +86-15623179893 wendy@hb-harvestchem.com China 931 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Hebei Jiangkai Trading Co., Ltd 0086-17197824289,17197824028 CHINA 260 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Shanghai Saikerui Biotechnology Co. , Ltd. 021-58000709 15900491054 info@scrbio.com China 9260 58

View Lastest Price from Drostanolone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dromostanolone pictures 2021-11-26 Dromostanolone
58-19-5
US $200.00-4000.00 / Kg/Drum 1Kg/Bag 99+ 1000kg Henan Tengzan Biotechnology Co. LTD
Drostanolone;dromostanolone  pictures 2018-09-26 Drostanolone;dromostanolone
58-19-5
US $8.00 / G 1G 99.8% skype:lila_1646 whatsapp:+8617197824208 500kg per week Hebei Jiangkai Trading Co., Ltd
  • Dromostanolone pictures
  • Dromostanolone
    58-19-5
  • US $200.00-4000.00 / Kg/Drum
  • 99+
  • Henan Tengzan Biotechnology Co. LTD
Drostanolone/Dromostanolone (5α)-2α-Methyl-4,5-dihydrotestosterone 17β-Hydroxy-2α-methyl-5α-androstan-3-one Medrotestron Metholone Dromostanolone (2a,5a,17b)-17-Hydroxy-2-methylandrostan-3-one (2R,5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-2,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one (2α,5α,17β)-17-Hydroxy-2-Methylandrostan-3-one 2α-Methyl-17β-hydroxy-5α-androstan-3-one 2α-Methyl-17β-hydroxyandrostan-3-one 2α-Methyl-5α-androstan-17β-ol-3-one 2α-Methyl-5α-dihydrotestosterone Dihydro-2α-Methyltestosterone Androstan-3-one,17-hydroxy-2-Methyl-, (2a,5a,17b)- Androstan-3-one, 17-hydroxy-2-methyl-, (2α,5α,17β)- 58-19-5 Dromostanolone DROSTANOLONE 5α-ANDROSTAN-2α-METHYL-17β-OL-3-ONE 58-19-5 Intermediates & Fine Chemicals Pharmaceuticals Steroids