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Raw Sex Drugs Powder Vardenafil Hormone

Raw Sex Drugs Powder Vardenafil Hormone

Vardenafil
CAS No: 224785-91-5
Alias: Fardenafil
MF: C23H33ClN6O4S
MW: 525.06

Products Specifications:

Quick Detail:
Vardenafil
CAS No: 224785-91-5
Alias: Fardenafil
MF: C23H33ClN6O4S
MW: 525.06
Appearance: White powder, odorless, taste bitter and astringent soluble in water and alcohol.
Use: It is pharmaceutical raw material, indicated for the treatment of erectile dysfunction


COA:

Test Items

Specification

Test Results

Description

White or almost white crystalline powder

White crystalline powder

Melting Point

191.0~193.0ºC

192ºC

Loss of drying

≤1.0%

0.5%

Heavy Metal

≤20ppm

15ppm

TLC

Only one spot

Only one spot

Assay

≥99.5%

99.61%

Conclusion

It complies with the USP 32.


The treatment of erectile dysfunction is a first-line treatment for erectile dysfunction. Developed by the German Bayer company, it was first launched in the US in 2002. Like sildenafil, it belongs to the second generation of type 5 phosphodiesterase inhibitors. It works very quickly and takes about 15~20 minutes. The effect is ten times stronger than that of sildenafil. Clinical data show that 50% to 60% of male diabetic patients over 50 years of age have erectile dysfunction, and erectile dysfunction caused by nerve and vascular injury caused by diabetes is particularly difficult to cure. Bayer, a powerful selective phosphodiesterase 5 (PDE5) inhibitor, is likely to bring the gospel to patients with erectile dysfunction caused by diabetes. As a one-time treatment drug, these drugs are taken orally about 1 hours before sexual life. By selectively inhibiting PDE5 and blocking the release of nitric oxide (NO) induced cGMP degradation after sexual stimulation, it improves the concentration, relaxes the arterial smooth muscle, strengthens the erectile function, and occasionally has a headache, blushing, stomach discomfort, and color. Adverse reactions such as disturbance of consciousness.

Three selective type 5 phosphodiesterase (PDE5) inhibitors: sildenafil (sildenus), favdenafil (eolda) and TDA are the first-line drugs for the treatment of ED; there is no significant difference between PDE5 inhibitors and apomorphine in the efficacy, safety, and tolerance of the drug; the injection of prostaglandins in the cavernous body E1 is a second-line treatment for ED, while prostaglandin E1 in the urethra is less effective than intravitreal injection of prostaglandin E1. It is concluded that PDE5 inhibitors are effective, well tolerated and safe in the treatment of ED, and the treatment of apomorphine, injection of prostaglandin E1 and urethral prostaglandin E1 in the urethra is also effective and is well tolerated.

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