| Identification | Back Directory | [Name]
4-chloro-17a-methyl-androst-1,4-diene-3,17b-diol | [CAS]
1338221-84-3 | [Synonyms]
HALODROL
4-chloro-17a-methyl-androst-1,4-diene-3,17b-diol
(3beta,17beta)-4-chloro-17-methyl-Androsta-1,4-diene-3,17-diol | [EINECS(EC#)]
-0 | [Molecular Formula]
C20H29ClO2 | [MOL File]
1338221-84-3.mol | [Molecular Weight]
336.896 |
| Chemical Properties | Back Directory | [Boiling point ]
465.5±45.0 °C(Predicted) | [density ]
1.20±0.1 g/cm3(Predicted) | [pka]
12.46±0.70(Predicted) | [InChIKey]
ZHWBNJVZZYSUJZ-HXKLKIPJNA-N | [SMILES]
C1(O)C(Cl)=C2[C@](C)(C=C1)[C@]1([H])[C@]([H])([C@@]3([H])[C@@](CC1)(C)[C@@](C)(O)CC3)CC2 |&1:5,9,11,13,15,19,r| |
| Hazard Information | Back Directory | [History]
As a synthetic, orally active anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of 4-androstenediol, 4-chloro-17a-methyl-androst-1,4-diene-3,17b-diol was never marketed. It was first encountered in 2005 when it was introduced as a dietary supplement and putative prohormone under the name Halodrol-50 by industry veteran, Bruce Kneller while working with the dietary supplement company, Gaspari Nutrition. | [Uses]
Halodrol is a 17-alpha alkylated steroid that converts to the steroid Oral Turinabol (C365220) after interacting with 3-β-HSD enzyme. Studies suggested the lack of progestational effects of Halodrol m
ay be due to the the 4-chloro group, where it restricts the interaction with aromatase enzyme to produce inactive 4-chloro-DHT metabolites, thus producing significantly less androgenic side effects. | [Side effects]
When taken by mouth: Halodrol-50 (4-chloro-17a-methyl-androst-1,4-diene-3,17b-diol) is possibly unsafe for most people when taken by mouth. Side effects include liver damage, infertility, behavioral changes, hair loss, and others. |
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| Company Name: |
Marco Hi-Tech
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+1-866-594-0010 |
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www.chemicalbook.com/ShowSupplierProductsList13141/0_EN.htm |
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