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PRILIGY

Dapoxetine hydrochloride

CAS: 129938-20-1

Molecular Formula: C21H23NO·HCl

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PRILIGY - Names and Identifiers

Name Dapoxetine hydrochloride
Synonyms PRILIGY
Priligy
LY-21044
DAPOXETINE HCL
Rimonabant 75000
DL-Dapoxteine HCL
(S)-N,N-dimethyl-3-
LY-210448 hydrochloride
LY-210448 HYDROCHLORIDE
Dapoxetine hydrochloride
Hydrochloric acid Dapoxetine
N,N-DiMethyl-1-phenyl-3-(1-naphthalenyloxy)propanaMinehydrochloride
(S)-N,N-dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride
(S)-N,N-Dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride
(1S)-N,N-Dimethyl-3-naphthalen-1-yloxy-1-phenyl-propan-1-amine hydrochloride
(S)-n,n-dimethyl-3-(naphthalene-1-yloxy)-1-phenylpropan-1-amine hydrochloride
((S)-(+)-N,N-Dimethyl-1-phenyl-3-(1-naphthalenyloxy)propanamine hydrochloride)
(S-(+)-N,N-Dimethyl-a-[2-(naphthalenyloxy)ethyl]benzenemethanamine hydrochloride
(S-(+)-N,N-dimethyl-a-[2-(naphthalenyloxy)ethyl] benzenemethanamine hydrochloride
CAS 129938-20-1
EINECS 640-411-8
InChI InChI=1/C21H23NO.ClH/c1-22(2)20(18-10-4-3-5-11-18)15-16-23-21-14-8-12-17-9-6-7-13-19(17)21;/h3-14,20H,15-16H2,1-2H3;1H

PRILIGY - Physico-chemical Properties

Molecular FormulaC21H23NO·HCl
Molar Mass341.88
Melting Point175-1790C
Boling Point480.5°C at 760 mmHg
Specific Rotation(α)D +135.78° (c = 2.18 in methanol)
Flash Point244.4°C
Solubility Soluble in DMSO (68 mg/ml at 25 °C), chloroform, methanol, water (68 mg/ml at 25 °C)
Vapor Presure1.27E-09mmHg at 25°C
AppearanceYellow powder
Colorwhite
Merck14,2821
Storage Conditionroom temp
MDLMFCD08272809
UseA selective serotonin reuptake inhibitor
In vitro studyDapoxetine not only reduced the Kv4.3 peak current but also accelerated the current inactivation decay rate in a concentration-dependent manner. Dapoxetine reduces the duration of the past polarization pulse of Kv4.3 current, IC 50 is 5.3 μm. Dapoxetine also caused an accelerated inactivation of a large number of off-states. Dapoxetine produced a significant use-dependent block with delayed recovery from inactivation of the Kv4.3 current. Dapoxetine reduced the peak amplitude of the current at Kv1.5 and accelerated the decay rate of current inactivation in a concentration-dependent manner, with IC 50 at 11.6 μm. Dapoxetine reduces the tail current amplitude and slows down the inactivation process of Kv1.5, which leads to the phenomenon of tail penetration. Dapoxetine produced a use-dependent Kv1.5 block at 1 and 2Hz frequencies and slowed the recovery of time-course inactivation. Dapoxetine also appears to be a useful adjunct to morphine, lowering the analgesic threshold, although Dapoxetine itself has negligible analgesic activity. Dapoxetine is the D-enantiomer LY243917, which is 3.5 times more potent as a serotonin reuptake inhibitor than the L-enantiomer.

PRILIGY - Risk and Safety

Risk CodesR22 - Harmful if swallowed
R36 - Irritating to the eyes
R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
Safety DescriptionS36 - Wear suitable protective clothing.
S60 - This material and its container must be disposed of as hazardous waste.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
UN IDsUN 3077 9 / PGIII
WGK Germany3
HS Code29221990

PRILIGY - Introduction

Dapoxetine HCl is a short-acting, novel selective serotonin reuptake inhibitor.
Last Update:2022-10-16 17:13:08
PRILIGY
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Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
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Multiple SpecificationsSpot supply
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Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
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Product Name: Dapoxetine hydrochloride Request for quotation
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Tel: 0086-551-65418684
Email: sales@tnjchem.com
     info@tnjchem.com
Mobile: 0086 189 4982 3763
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Wechat: 189 4982 3763
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Shanghai Yuanye Bio-Technology Co., Ltd.
Spot supply
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CAS: 129938-20-1
Tel: 18301782025
Email: 3008007409@qq.com
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