129938-20-1 Dapoxetine Hydrochloride Factory Supply 99% Purity Powder

China 129938-20-1 Dapoxetine Hydrochloride Factory Supply 99% Purity Powder, Find details about China Dapoxetine Hydrochloride, Hydrochloride Powder 129938-20-1 from 129938-20-1 Dapoxetine Hydrochloride Factory Supply 99% Purity Powder

Model NO.
129938-20-1
Melting Point
175-1790c
Alpha
D +135.78° (C = 2.18 in Methan)
Storage Temp.
Room Temp
Solubility
DMSO: ≥20mg/Ml
Form
Powder
Color
White
Optical Activity
[α]/D +125 to +135°, C = 1 in Methan
Merck
14,2821
CAS Database Reference
129938-20-1(CAS Database Reference)
Trademark
hanhong
Transport Package
Customized
Specification
base on product form
Origin
Wuhan
HS Code
29221990
Model NO.
129938-20-1
Melting Point
175-1790c
Alpha
D +135.78° (C = 2.18 in Methan)
Storage Temp.
Room Temp
Solubility
DMSO: ≥20mg/Ml
Form
Powder
Color
White
Optical Activity
[α]/D +125 to +135°, C = 1 in Methan
Merck
14,2821
CAS Database Reference
129938-20-1(CAS Database Reference)
Trademark
hanhong
Transport Package
Customized
Specification
base on product form
Origin
Wuhan
HS Code
29221990
129938-20-1 Dapoxetine Hydrochloride Factory Supply 99% Purity Powder
Product Description

Description

Dapoxetine, 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. Dapoxetine 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, dapoxetine was initially created as an antidepressant. However, unlike other SSRIs, dapoxetine 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, dapoxetine 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. Dapoxetine has been sold in several European and Asian countries, and lately in Mexico. In the US, dapoxetine 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.

Basic Info

Chemical Name

Dapoxetine Hydrochloride

Synonyms

(1S)-N,N-dimethyl-3-naphthalen-1-yloxy-1-phenylpropan-1-amine,hydrochloride;(S)-N,N-Dimethyl-α-[2-(1-naphthyloxy)ethyl]benzylamine Hydrochloride;(S)-N,N-Dimethyl-3-(1-naphthyloxy)-1-phenylpropylamine Hydrochloride;Dapoxetine HCl;(S)-N,N-Dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride;

CAS No.

129938-20-1

Molecular Formula

C21H24ClNO

Molecular Weight

341.87400

PSA

12.47000

LogP

5.71360

Numbering system

MDL numberMFCD08272809

Properties

Appearance & Physical State

White to off-white crystalline solid

Boiling Point

454.4ºC at 760 mmHg

Melting Point

175-179ºC

Flash Point

132.6ºC

Vapor Pressure

1.27E-09mmHg at 25°C

Safety Info

HS Code

2922199090

Symbol

GHS07

Signal Word

Warning

Caution Statement

P305 + P351 + P338

Hazard Declaration

H302; H319; H413
 
Detailed Photos

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