(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(R)-6-methyl-2-heptyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-amine
≥95%
- Product Code: 237617
CAS:
2126-93-4
Molecular Weight: | 385.67 g./mol | Molecular Formula: | C₂₇H₄₇N |
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EC Number: | MDL Number: | MFCD11618119 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C, light-proof, inert gas |
Product Description:
Used primarily in the synthesis of steroid-based pharmaceuticals, this compound serves as a key intermediate in the production of hormones with applications in endocrinology and reproductive health. Its structure allows for selective modification to create biologically active steroids, including those used in hormone replacement therapy, treatment of hormonal disorders, and anti-inflammatory agents. Due to its chiral centers and specific stereochemistry, it enables precise control in synthesizing active ingredients for medications targeting metabolic, immune, and developmental pathways. It is also employed in research settings to develop novel steroid analogs with improved efficacy and reduced side effects.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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25mg | 10-20 days | ฿24,000.00 |
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50mg | 10-20 days | ฿35,560.00 |
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100mg | 10-20 days | ฿53,350.00 |
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(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(R)-6-methyl-2-heptyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-amine
Used primarily in the synthesis of steroid-based pharmaceuticals, this compound serves as a key intermediate in the production of hormones with applications in endocrinology and reproductive health. Its structure allows for selective modification to create biologically active steroids, including those used in hormone replacement therapy, treatment of hormonal disorders, and anti-inflammatory agents. Due to its chiral centers and specific stereochemistry, it enables precise control in synthesizing active ingredients for medications targeting metabolic, immune, and developmental pathways. It is also employed in research settings to develop novel steroid analogs with improved efficacy and reduced side effects.
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