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Home > products > API Active Pharmaceutical Ingredient > Flibanserin CAS 167933-07-5 API Active Pharmaceutical Ingredient

Flibanserin CAS 167933-07-5 API Active Pharmaceutical Ingredient

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 167933-07-5

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Price: Negotiation

Packaging Details: Bag,Drum

Delivery Time: 7-15DAY

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CAS 167933-07-5 Flibanserin

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CAS 167933-07-5

CAS NO::
167933-07-5
Appearance::
White Powder
Molecular Formula::
C20H21F3N4O
Molecular Weight::
390.40200
EINECS NO::
643-002-2
MDL NO::
MFCD00918402
CAS NO::
167933-07-5
Appearance::
White Powder
Molecular Formula::
C20H21F3N4O
Molecular Weight::
390.40200
EINECS NO::
643-002-2
MDL NO::
MFCD00918402
Flibanserin CAS 167933-07-5 API Active Pharmaceutical Ingredient

Product Description:

Product Name: Flibanserin CAS NO: 167933-07-5          


Synonyms:

1,3-Dihydro-1-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)-2H-benzimidazol-2-one;

1-(2-(4-(3-Trifluoromethylphenyl)piperazin-1-yl)ethyl)benzimidazol(1H)-2-one;

3-[2-[4-[4-(trifluoromethyl)phenyl]piperazin-1-yl]ethyl]-1H-benzimidazol-2-one;


Chemical & Physical Properties:

Appearance: White powder

Assay :≥99.0%

Density: 1.292 g/cm3

Refractive Index: 1.566

Storage Temp.: 2-8℃

Solubility: DMSO: soluble10mg/mL, clear


Safety Information:

Symbol: GHS06

Hazard Declaration: H301; H315; H319; H335

Caution Statements: P261; P301 + P310; P305 + P351 + P338

Signal Word: Danger


Flibanserin, sold under the trade name Addyi, is a medication approved for the treatment of pre-menopausal women with hypoactive sexua/l desire disorder (HSDD). The medication increases the number of satisfying sexua/l events per month by about one half over placebo from a starting point of about two to three. The certainty of the estimate is low. The side effects of dizziness, sleepiness, and nausea occur about three to four times more often.

Development by Boehringer Ingelheim was halted in October 2010 following a negative evaluation by the U.S. Food and Drug Administration. The rights to the drug were then transferred to Sprout Pharmaceuticals, which achieved approval of the drug by the US FDA in August 2015.

HSDD was recognized as a distinct sexua/l function disorder for more than 30 years, but was removed from the Diagnostic and Statistical Manual of Mental Disorders in 2013, and replaced with a new diagnosis called female sexua/l interest/arousal disorder (FSIAD).


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