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Pharmaceutical Raw Materials Sex Enhancement Series Flibanserin for Muscle Gain 167933-07-5

CATEGORY AND TAGS:
Sex-enhancement items
Certification: ISO9001,Kosher, COA
Model Number: 167933-07-5
Minimum Order Quantity: 1kg
Delivery Time: 4-7 days
Payment Terms: T/T, Western Union, MoneyGram,Bitcoin
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  • Specifications

Pharmaceutical Raw Materials Sex Enhancement Series Flibanserin for Muscle Gain 167933-07-5

Abstract

CAS:167933-07-5
MF:C20H21F3N4O
MW:390.4
EINECS:1806241-263-5
storage temp. 2-8°C
solubility DMSO: soluble10mg/mL, clear
color white to beige
Hazard statements H301-H315-H319-H335
Precautionary statements P261-P301+P310-P305+P351+P338
Hazard Codes T
Risk Statements 25-36/37/38
Safety Statements 26-45

Description

Flibanserin is used for hypoactive sexual desire disorder among women. Those receiving flibanserin report a 0.5 increase compared to placebo in the number of times they had “satisfying sexual events”.In those on flibanserin it rose from 2.8 to 4.5 times a month while women receiving placebo reported also an increase of “satisfying sexual events” from 2.7 to 3.7 times a month.The onset of the flibanserin effect was seen from the first timepoint measured after 4 weeks of treatment and maintained throughout the treatment period.

The effectiveness of flibanserin was evaluated in three phase 3 clinical trials. Each of the three trials had two co-primary endpoints, one for satisfying sexual events (SSEs) and the other for sexual desire. Each of the 3 trials also had a secondary endpoint that measured distress related to sexual desire.

Application

Flibanserin is used for hypoactive sexual desire disorder among women. Those receiving flibanserin report a 0.5 increase compared to placebo in the number of times they had “satisfying sexual events”. In those on flibanserin it rose from 2.8 to 4.5 times a month while women receiving placebo reported also an increase of “satisfying sexual events” from 2.7 to 3.7 times a month.The onset of the flibanserin effect was seen from the first timepoint measured after 4 weeks of treatment and maintained throughout the treatment period.

COA

Testing Items Specifications Results
Characteristics An off-white to white powder Complied
Identification Meet the requirements Positive
Loss on Drying ≤0.50% 0.13%
Heavy Metals ≤20PPM <20PPM
Purity (by HPLC) ≥99.0% 99.2%
Conclusion: The commodity is complied with the standard of the factory

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