Hair Loss Treatment Finasteride Powder CAS 98319-26-7

Product Details:

Place of Origin: China
Brand Name: Changland
Certification: GMP&ISO
Model Number: 98319-26-7

Payment & Shipping Terms:

Minimum Order Quantity: 100g
Price: USD 385 Per 100g,USD 2000 Per 1Kg
Packaging Details: 1KG per foil bag, 25KG per drum.
Delivery Time: 5 working days
Payment Terms: MoneyGram, Western Union, T/T, D/P, D/A, L/C
Supply Ability: 200KG per month

Description

Hair Loss Treatment Finasteride Powder CAS 98319-26-7

Description

Cas: 98319-26-7 MF: C23H36N2O2
MW: 372.54 EINECS No.: 620-534-3
Boiling Point: 576.6±50.0 °C(Predicted) Melting Point: 253 °C
Density: 1.065±0.06 G/cm3(Predicted) Color: White
Storage: Room Temp Sample: Available
High Light:

98319-26-7 Finasteride Powder

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Hair Loss Treatment Finasteride Powder

 

Hair Loss Treatment CAS 98319-26-7 Finasteride High Quality Factory Supply Powder

 

Product introduction

 

Product name Finasteride
CAS No. 98319-26-7
MF C23H36N2O2
MW 372.54
EINECS No. 620-534-3
Density 1.065±0.06 g/cm3(Predicted)
Boiling Point 576.6±50.0 °C(Predicted)
Melting Point 253 °C

 

Description:

 

Finasteride is an approved medication for the treatment of hair loss in men.

 

Application Area:

 

Benign prostatic hyperplasia

Male pattern baldness

 

Use&function:

Finasteride is a 4-azasteroid that is a specific inhibitor of the intracellular enzyme type II 5a-reductase in the metabolism of testosterone to the more potent dihydrotestosterone. Benign prostatic hyperplasia or benign prostatic hyperplasia depends on the conversion of testosterone to dihydrotestosterone in the prostate. This medicine is very effective in reducing dihydrotestosterone in the blood and prostate. Finasteride has no affinity for androgen receptors.
In the Long-Term Efficacy and Safety Study (PLESS), 3016 patients with moderate-to-severe symptoms of benign prostatic hyperplasia were treated for 4 years for BPH-related urologic procedures (surgical interventions), such as transurethral Prostatectomy and other prostatectomy, or acute urinary retention requiring catheterization were evaluated. In this double-blind, randomized, placebo-controlled, multicenter study, treatment with the drug reduced the overall risk of urologic disposition by 51%, with significant and sustained reduction in prostate volume and sustained maximal urine output Increased flow and improved symptoms.