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Dapoxetine hydrochloride

CAS No.
129938-20-1
Chemical Name:
Dapoxetine hydrochloride
Synonyms
DAPOXETINE HCL;Dapoxetin HCl;Priligy;DL-Dapoxteine HCL;Dapoxetine HCL (Priligy);LY-21044;LY-210448;Dapoxetine HCI;Rimonabant 75000;Dapoxetine HCL-IHS
CBNumber:
CB7104314
Molecular Formula:
C21H24ClNO
Molecular Weight:
341.88
MDL Number:
MFCD08272809
MOL File:
129938-20-1.mol
MSDS File:
SDS
Last updated:2024-04-15 18:41:30

Dapoxetine hydrochloride Properties

Melting point 175-1790C
alpha D +135.78° (c = 2.18 in methanol)
storage temp. room temp
solubility DMSO: ≥20mg/mL
form powder
color white
optical activity [α]/D +125 to +135°, c = 1 in methanol
Merck 14,2821
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/t20-;/s3
InChIKey IHWDIQRWYNMKFM-OZYVVJTJNA-N
SMILES O(C1=CC=CC2C=CC=CC1=2)CC[C@@H](C1C=CC=CC=1)N(C)C.Cl |&1:13,r|
CAS DataBase Reference 129938-20-1(CAS DataBase Reference)
FDA UNII U4OHT63MRI

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H319-H413
Precautionary statements  P305+P351+P338
Hazard Codes  Xn,N
Risk Statements  22-36-50/53
Safety Statements  36-60-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
HS Code  29221990
NFPA 704
0
2 0

Dapoxetine hydrochloride price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D7071 Dapoxetine hydrochloride ≥98% (HPLC) 129938-20-1 10mg $118 2024-03-01 Buy
Sigma-Aldrich D7071 Dapoxetine hydrochloride ≥98% (HPLC) 129938-20-1 50mg $277.2 2024-03-01 Buy
TCI Chemical D4761 Dapoxetine Hydrochloride >98.0%(HPLC) 129938-20-1 1g $55 2024-03-01 Buy
TCI Chemical D4761 Dapoxetine Hydrochloride >98.0%(HPLC) 129938-20-1 5g $161 2024-03-01 Buy
Cayman Chemical 9002488 Dapoxetine (hydrochloride) ≥98% 129938-20-1 1mg $81 2024-03-01 Buy
Product number Packaging Price Buy
D7071 10mg $118 Buy
D7071 50mg $277.2 Buy
D4761 1g $55 Buy
D4761 5g $161 Buy
9002488 1mg $81 Buy

Dapoxetine hydrochloride Chemical Properties,Uses,Production

Description

Dapoxetine hydrochloride, belonging to the class of SSRIs, was the first drug originally approved for the on-demand treatment of men with PE by seven European countries in 2008.
Premature ejaculation (PE) is the most common male sexual dysfunction. Dapoxetine is a short-acting SSRI. It is differentiated from the existing SSRI treatments for PE by the fact that it can be administered on an as-needed basis. In healthy subjects, dapoxetine is rapidly absorbed after oral administration with a peak plasma concentration (Tmax) occurring between 1.4 and 2h.

Chemical Properties

Dapoxetine hydrochloride is a white to slightly yellow powder. It is freely soluble in methanol, propylene glycol, some organic solvents (eg. N,N-dimethylformamide) , slightly soluble in ethanol and almost insoluble in water. It is a BCSI class II compound, and poor solubility is a key factor affecting the difference in clinical efficacy. Dapoxetine hydrochloride exists in various crystal forms, the solubility of different crystal forms is quite different, and there is a phenomenon of phase and transformation between crystal forms.

Originator

Lilly (US)

Uses

Dapoxetine hydrochloride is a short-acting novel selective serotonin reuptake inhibitor marketed for the treatment of premature ejaculation in men. Premature ejaculation (PE) is the most common male sexual disorder, estimated to affect up to 30% of men.

brand name

Priligy

General Description

Dapoxetine ((+)-(S)-N,N-dimethyl-(α)-[2(1naphthal enyloxy)ethyl]-benzenemethanamine hydrochloride) possess a similar structure as that of fluoxetine.

Biochem/physiol Actions

Potent Selective serotonin reuptake inhibitor (SSRI); used in treatment of premature ejaculation

Synthesis

Dapoxetine can be synthesized in four chemical steps starting from R-1phenyl- 1,3-propanediol via selective tosylation of the primary hydroxy group with p-toluenesulfonyl chloride, triethylamine and 4-(dimethylamino) pyridine (DMAP), and subsequent condensation with 1naphthol by means of sodium- or lithium hydroxide to yield R-3-(1naphthyloxy)- 1-phenylpropanol as the key intermediate. Conversion of the alcohol group to the corresponding mesylate with methanesulfonyl chloride, triethylamine, and DMAP, followed by treatment with dimethylamine affords dapoxetine, which is then acidified to its hydrochloride salt.

storage

room temperature (desiccate)

Mode of action

The mechanism of action of dapoxetine in premature ejaculation is presumed to be linked to the inhibition of neuronal reuptake of serotonin and the subsequent potentiation of the neurotransmitter's action at pre- and post-synaptic receptors. Dapoxetine is a centrally-acting SSRI that modulates serotonin levels in relevant areas such as the lateral paragigantocellular nucleus through inhibition of the serotonin transporter (SERT). This compound also decreases peak amplitude and accelerates the decay rate of current inactivation in a variety of voltage-gated K+ channels.

Dapoxetine hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Dapoxetine hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DapoxetineHydrochloride pictures 2024-04-25 DapoxetineHydrochloride
129938-20-1
US $1.00-80.00 / g 1g 99.99% 1000kg Wuhan Cell Pharmaceutical Co., Ltd
Dapoxetine HCL pictures 2024-04-25 Dapoxetine HCL
129938-20-1
US $80.00 / kg 1kg 99.99% 2 tons Wuhan Cell Pharmaceutical Co., Ltd
Dapoxetine HCI pictures 2024-04-25 Dapoxetine HCI
129938-20-1
US $1.00-72.00 / g 1g 99.99% 1000kg Wuhan Cell Pharmaceutical Co., Ltd
  • Dapoxetine HCL pictures
  • Dapoxetine HCL
    129938-20-1
  • US $80.00 / kg
  • 99.99%
  • Wuhan Cell Pharmaceutical Co., Ltd
  • Dapoxetine HCI pictures
  • Dapoxetine HCI
    129938-20-1
  • US $1.00-72.00 / g
  • 99.99%
  • Wuhan Cell Pharmaceutical Co., Ltd
Dapoxetine hydrochloride (1S)-N,N-Dimethyl-3-naphthalen-1-yloxy-1-phenyl-propan-1-amine hydrochloride S-(+)-N,N-dimethyl-a-[2-(naphthalenyloxy)ethyl] benzenemethanamine hydrochloride, LY-210448 hydrochloride Mixed spin Dapoxetine (1s)-n,n-dimethyl-3-naphthalen-1-yloxy-1-phenyl-propan-1-amine hydrochloride Rimonabant 75000 (aS)-N,N-Dimethyl-a-[2-(1-naphthalenyloxy)ethyl]benzenemethanamine LY-21044 ((S)-(+)-N,N-Dimethyl-1-phenyl-3-(1-naphthalenyloxy)propanamine hydrochloride) (S)-(+)--N,N-Dimethyl-1-phenyl-3-(1-naphthalenyloxy)propanamine Dapoxetine hydrochloride (aS)-N,N-Dimethyl-α-[2-(1-naphthalenyloxy)ethyl]benzenemethanamine LY-210448 Dapoxetine hcl for R&D naphthalen-1-yloxy-1-phenyl-propan-1-amine hydrochloride (S)-Dapoxetine hydrochloride (αS)-N,N-DiMethyl-α-[2-(1-naphthalenyloxy)ethyl]benzeneMethanaMine Dapoxetine hydrochloride|S1869 Dapoxetine hydrochloride(Priligy) N,N-DiMethyl-1-phenyl-3-(1-naphthalenyloxy)propanaMinehydrochloride (S)-N,N-Dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride D-(+)N,N-diMethyl-3-(naphthalen-1-yloxy) (αS)- N,N-dimethyl-α-[2-(1-naphthalenyloxy)ethyl]-benzenemethanamine, hydrochloride (1:1) (6R,7R)-7-Amino-8-oxo-3-(1-propenyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidDapoxetine hydrochloride Benzenemethanamine, N,N-dimethyl-α-[2-(1-naphthalenyloxy)ethyl]-, hydrochloride, (S)- (S)-N,N-DIMETHYL-Α-[2-(1-NAPHTHALENY-LOXY)ETHYL]BENZENEMETHANAMINE HYDROCHLORIDE Dapoxetine hydrochloride, 98%, a short-acting novel selective serotonin reuptake inhibitor DapoxetineHydrochloride> Dapoxetine hydrochloride,>98% Dapoxetine Hydrochlorid Salt (S)-N,N-Dimethyl-3-(1-naphthyloxy)-1-phenylpropylamine Hydrochloride (S)-N,N-Dimethyl-alpha-[2-(1-naphthyloxy)ethyl]benzylamine Hydrochloride Dapoxetine hydrochloride USP/EP/BP Hydrochloride Dapoxetine Right-handed poxetine Dapoxetine HCI Dapoxetine HCL-IHS Dapoxetine HCl (LY-210448 HCl) Dapoxetine HydrochlorideQ: What is Dapoxetine Hydrochloride Q: What is the CAS Number of Dapoxetine Hydrochloride Q: What is the storage condition of Dapoxetine Hydrochloride Q: What are the applications of Dapoxetine Hydrochloride Dapoxetine/Dapoxetine HCl/Dapoxetine hydrochloride LY-210448 hydrochloride PRILIGY;LY-210448 HYDROCHLORIDE (S)-N,N-dimethyl-3- D-Dapoxetine Hydrochloride DAPOXETINE HCL Dapoxetin HCl Dapoxetine HCL (Priligy) DAPOXETINE HYDROCHLORIDE CHEMISTRY PURE 98.5% HPLC DL-Dapoxteine HCL Priligy Dapoxetine / Priligy Dapoxetine HCl Powder Dapoxetine Hydrochloride, ≥ 98.0% 129938-20-1 1299-20-1 C21H23NOClH C21H23NOHCl Amines Aromatics