Product Details:
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CAS: | 98319-26-7 | Apparence: | Almost White Crystalline Powder |
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Alias: | Finasteride, Proscar | Exact Mass: | 372.27800 |
PSA: | 58.20000 | Density: | 1.065 G/cm3 |
Oral Finasteride For Sex Enhancement Powder,CAS 98319-26-7.
Quick detail
Finasteride | |
CAS No.: | 98319-26-7 |
Synonyms: | Finastid; Propecia; Proscar; Finasteride; Finpecia; Prostide; Chibro-Proscar; Finasteridum; |
Formula: | C23H36N2O2 |
Exact Mass: | 372.27800 |
Molecular Weight: | 372.54400 |
PSA: | 58.20000 |
LogP: | 4.53420 |
Appearance : | white to off-white crystalline powder |
Density: | 1.065 g/cm3 |
Melting Point: | 253ºC |
Boiling Point: | 576.6ºC at 760 mmHg |
Flash Point: | 177.4ºC |
Refractive Index: | 1.524 |
Water Solubility: | insoluble |
Finasteride Description:
Finasteride, sold under the brand names Proscar and Propecia among others, is a medication used for the treatment of benign prostatic hyperplasia (BPH) and male pattern baldness (MPB). It is a type II and type III 5α-reductase inhibitor; 5α-reductase, an enzyme, converts testosterone to dihydrotestosterone (DHT).
Finasteride Usages
Usage 1 | It can reduce of DHT synthesis, |
Usage 2 | It can reduce the content of scalp hair and serum dihydrotestosterone |
Usage 3 | It can recovery has been suppressed follicular papilla, |
Usage 4 | It can promote hair growth and prevent hair loss |
Description:
1. as a new fast SSRI, a short half life, a selective 5 - HT reuptake inhibitor (SSRI), for
the treatment of premature ejaculation and erectile dysfunction. is a selective 5 - HT
reuptake inhibitor (SSRI), such drugs widely used to treat depression and related affective
disorders.
2. , marketed as (among and other brands) is the first compound developed
specially for the treatment of premature ejaculation in men 18-64 years old. works by
inhibiting the serotonin transporter, increasing serotonin's action at the post synaptic cleft, and as
a consequence promoting ejaculatory delay. As a member of selective serotonin reuptake
inhibitor (SSRI) family, was initially created as an antidepressant. However, unlike
other SSRIs, is absorbed and eliminated rapidly in the body. Its fast acting property
makes it suitable for the treatment of PE but not as an antidepressant.
3. Treat male premature ejaculation and erectile dysfunction. Because lack of specific approval
treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine,
sertraline, fluvoxamine, and citalopram have been used as off label drugs to treat PE.
Description:
1. as a new fast SSRI, a short half life, a selective 5 - HT reuptake inhibitor (SSRI), for
the treatment of premature ejaculation and erectile dysfunction. is a selective 5 - HT
reuptake inhibitor (SSRI), such drugs widely used to treat depression and related affective
disorders.
2. , marketed as (among and other brands) is the first compound developed
specially for the treatment of premature ejaculation in men 18-64 years old. works by
inhibiting the serotonin transporter, increasing serotonin's action at the post synaptic cleft, and as
a consequence promoting ejaculatory delay. As a member of selective serotonin reuptake
inhibitor (SSRI) family, was initially created as an antidepressant. However, unlike
other SSRIs, is absorbed and eliminated rapidly in the body. Its fast acting property
makes it suitable for the treatment of PE but not as an antidepressant.
3. Treat male premature ejaculation and erectile dysfunction. Because lack of specific approval
treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine,
sertraline, fluvoxamine, and citalopram have been used as off label drugs to treat PE.
Description:
1. as a new fast SSRI, a short half life, a selective 5 - HT reuptake inhibitor (SSRI), for
the treatment of premature ejaculation and erectile dysfunction. is a selective 5 - HT
reuptake inhibitor (SSRI), such drugs widely used to treat depression and related affective
disorders.
2. , marketed as (among and other brands) is the first compound developed
specially for the treatment of premature ejaculation in men 18-64 years old. works by
inhibiting the serotonin transporter, increasing serotonin's action at the post synaptic cleft, and as
a consequence promoting ejaculatory delay. As a member of selective serotonin reuptake
inhibitor (SSRI) family, was initially created as an antidepressant. However, unlike
other SSRIs, is absorbed and eliminated rapidly in the body. Its fast acting property
makes it suitable for the treatment of PE but not as an antidepressant.
3. Treat male premature ejaculation and erectile dysfunction. Because lack of specific approval
treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine,
sertraline, fluvoxamine, and citalopram have been used as off label drugs to treat PE.
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