QSC RESEARCH GRADE
≥99% HPLC PurityMS ConfirmedJanoshik COAIn-House SPPS1-Region Domestic Shipping
What is Dutasteride?
Dutasteride is a dual inhibitor of both 5α-reductase Type I and Type II isoforms — unlike finasteride which is Type II-selective. Achieves >90% reduction in serum and scalp DHT. The more complete DHT suppression profile makes dutasteride a superior research tool for full 5α-reductase inhibition studies, intracrinology research, and comparative models against finasteride. Research use only.
Research Applications
Dual 5α-Reductase Inhibition
Type I + II combined inhibition — complete DHT suppression vs finasteride partial
Intracrinology Research
Tissue-specific androgen metabolism, local DHT production in prostate/scalp/skin
BPH & Prostate Research
Maximal DHT reduction, prostate volume, stromal-epithelial androgen signalling
Comparative Finasteride Studies
Dutasteride vs finasteride — Type I vs dual inhibition tissue effect comparison
Androgenetic Alopecia
Superior scalp DHT reduction vs finasteride — hair follicle sensitivity research
Quick Specs
| Form | Tablet — 1mg per tablet, 100-tablet bottle |
| CAS Number | 164656-23-9 |
| Molecular Formula | C₂₇H₃₀F₆N₂O₂ |
| Molecular Weight | 528.5 g/mol |
| Compound Type | Dual 5α-Reductase Inhibitor (Type I + II) |
| Purity | ≥99% by HPLC — every batch |
| Identity | MS molecular weight confirmed — every batch |
| COA | Janoshik-independent, publicly verifiable |
| Manufacture | In-house synthesis — Qingdao, China |
| Storage | Room temperature sealed | cool, dry storage |
| Shelf Life | 24 months unopened |
