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Home > products > API Active Pharmaceutical Ingredient > Dapoxe-tine CAS 119356-77-3

Dapoxe-tine CAS 119356-77-3

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 119356-77-3

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Bag,Drum

Delivery Time: 7-15 days

Payment Terms: L/C, D/A, T/T, Western Union

Supply Ability: TON

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Highlight:
CAS NO::
119356-77-3
Appearance::
White To Off-white Crystalline Powder
Molecular Formula::
C21H23NO
Molecular Weight::
305.41300
EINECS NO::
1308068-626-2
MDL NO::
MFCD00865355
CAS NO::
119356-77-3
Appearance::
White To Off-white Crystalline Powder
Molecular Formula::
C21H23NO
Molecular Weight::
305.41300
EINECS NO::
1308068-626-2
MDL NO::
MFCD00865355
Dapoxe-tine CAS 119356-77-3

Product Description:

Product Name: Dapoxe-tine CAS NO: 119356-77-3

 

 

Synonyms:

Priligy;

Dapoxetina;

(1S)-N,N-dimethyl-3-naphthalen-1-yloxy-1-phenylpropan-1-amine;

 

 

Chemical & Physical Properties:

Appearance: White to off-white crystalline powder

Assay :≥99.0%

Density: 1.081 g/cm3

Boiling Point: 454.4℃at 760mmHg

Flash Point: 132.6℃

Refractive Index: 1.607

Vapor Pressure: 1.91E-08mmHg at 25℃

 

 

Safety Information:

HS Code: 2922199090

 

 

Dapoxe-tine, marketed as Priligy and Westoxetin, among and other brands, is the first compound developed specially for the treatment of premature ejaculation (PE) in men 18–64 years old. Dapoxe-tine works by inhibiting the serotonin transporter, increasing serotonin's action at the post synaptic cleft, and as a consequence promoting ejaculatory delay. As a member of selective serotonin reuptake inhibitor (SSRI) family, dapoxe-tine was initially created as an antidepressant. However, unlike other SSRIs, dapoxe-tine is absorbed and eliminated rapidly in the body. Its fast acting property makes it suitable for the treatment of PE but not as an antidepressant.

Originally created by Eli Lilly pharmaceutical company, dapoxe-tine was sold to Johnson & Johnson in 2003 and submitted as a New Drug Application to the Food and Drug Administration (FDA) for the treatment of PE in 2004. Dapoxe-tine has been sold in several European and Asian countries, and lately in Mexico. In the US, dapoxe-tine has been stuck in phase III development since 2003. However, it is expected to be marketed soon. In 2012, Menarini acquired the rights to commercialise Priligy in Europe, most of Asia, Africa, Latin America and the Middle East.

 

 

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