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| Product: | Tadalafil/ Cialis | CAS: | 171596-29-5 |
|---|---|---|---|
| Appearance: | White Crystalline Powder | Assay: | 99.82% |
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| Product Name | Tadalafil (Cialis) |
| Other Names | Tadalafil Citrate, Tadalafei |
| CAS | 171596-29-5 |
| MF | C22H19N3O4 |
| MW | 389.4 |
| EINECS | 200-835-2 |
| Categories | Active Pharmaceutical Ingredients;Cnbio;Erectile Dysfunction;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;API’s;Steroid and Hormone;Inhibitor;API;Tadalafil;NUCYNTA |
| Usage | 1, Used for the treatment of erectile dysfunction. A phosphodiesterase 5 inhibitor. 2, Analgesic, norepinephrine uptake blocker, mu-opiod receptor agonist |
| Assay | 99.82% |
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Tadalafil is a PDE5 inhibitor marketed in pill form for treating erectile dysfunction (ED) under the name Tadalafil, and under the name Adcirca for the treatment of pulmonary arterial hypertension. Tadalafil’s pharmacologic distinction is its longer half-life (17.50 hours) resulting in longer duration of action, and so partly responsible for “The Weekend Pill” sobriquet. Furthermore, the longer half-life is the basis for current investigation of tadalafil’s daily therapeutic use in relieving pulmonary arterial hypertension.
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There are limited side effects associated with its use. The most common side effects are headache, upset stomach, back pain, and muscle aches, and usually subside with in a few hours. Tadalafil was also found to be significantly higher at the end of the month, due to increased sexual activity. Buy Cialis (tadalafil) powder
Tadalafil (Cialis) Quality Test Report(COA):
| Product | Tadalafil | Batch Size | 95kgs |
| Batch No. | 20151108 | Report Date | 2015-11-15 |
| Manufacture Date | 2015-11-04 | Expiration Date | 2017-11-08 |
| Items | Enterprise | Result | |
| Description | Off-white or white crystalline powder | White crystalline powder | |
| Identification | IRHPLC | Conform to standard | |
| Loss on drying | ≤0.5% | 0.1% | |
| Residue on ignition | ≤0.1% | 0.03% | |
| Heavy metals | ≤0.002% | ＜0.002% | |
| Related substances(HPLC) | Individual impurity≤0.1% | 0.03% | |
| Total impurities≤0.3% | ≤0.3% | ||
| Assay(non-aqueous titration) | 97.5—102.5% | 99.82% | |
| Conclusion | Conform with Enterprise standard. | ||
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