|Place of Origin:||China|
|Model Number:||Amino Tadalafil|
|Minimum Order Quantity:||1KG|
|Packaging Details:||Aluminum foil bag|
|Payment Terms:||L/C, D/A, D/P, T/T, Western Union, MoneyGram，Alibaba Assurance Order|
|Einecs No.:||N/A||Appearance:||White Or Off-white Powder|
385769-84-6 Sexual Enhancement Powder Amino Tadalafil Powder
The Introductction of Amino Tadalafil
Amino Tadalafil is an analogue of Tadalafil.
Amino Tadalafil is a novel 5-hydroxytryptamine (5-HT) reuptake inhibitor, a water-soluble white or off-white powder, which has aphrodisiac and time-delaying effects for the treatment of sexual dysfunction.
By inhibiting the 5-HT transporter, Amino Tadalafil can effectively inhibit 5-HT reuptake, increase the concentration of 5-HT in the synaptic gap, activate the postsynaptic membrane 5-HT2C and 5-HT1A receptors, and exert delayed ejaculation effects, thus effectively controlling the symptoms of premature ejaculation in men.
Side effects of Amino Tadalafil include low blood pressure, headache, vomiting, dizziness, and temporary blurred vision. Improper use of tadalafil may pose serious health risks, especially for patients with heart problems.
Amino Tadalafil has the effect of dilating blood vessels, promoting normal contraction of penile smooth muscle, and increasing the amount of blood filling in the cavernous body of the penis.
Amino Tadalafil is commonly used in clinical practice to treat erectile weakness and erectile dysfunction caused by sexual dysfunction.
Amino Tadalafil can not only treat erectile dysfunction, but also has a certain effect on the treatment of lower urinary tract symptoms in elderly men. Tadalafil tablets can be preferred for the treatment of elderly men with lower urinary tract symptoms such as frequent urination and incomplete urination, combined with erectile dysfunction.
|PRODUCT NAME: Tadalafil|
|BATCH NO.:HNB2022011601||CAS No:171596-29-5|
|CHECKING DATE:2022-01-20||REPORT DATE : 2022-01-22|
|MANUFACTURE DATE: 2022-01-16||EXPIRY DATE : 2024-01-15|
|STANDARD:EP 9(EP 9 Specification)|
|ITEM OF ANALYSIS||STANDARD||RESULT|
|Appearance||White or almost white crystalline powder||White crystalline powder|
|Practically insoluble in water, freely soluble in dimethyl sulfoxide, slightly soluble in methylene chloride||
The infrared absorption spectrum is
concordant with the reference spectrum
|Identification||The principal peak in the chromatogram obtained with the test solution is similar in retention time and size to the principal peak in the chromatogram obtained with reference solution||Conforms|
|Rotation||+ 78.0°to + 84.0°||+80.6°|
|Impurities A, B and C||Impurity A, B and C≤0.1%||Non-detected|
|Loss on drying||≤0.5%||0.2%|
|Residue on ignition||≤0.1%||0.01%|
|Related Substances||individual impurity≤0.1%||0.08%|
|Related Substances||Total unknown impurity≤1.0%||0.10%|
|Residual Solvents||Methyl acetate≤0.5%||Non-detected|
|Conclusion||The test results conform with EP 9 Specification.|