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Paroxetine hydrochloride

CAS No.
78246-49-8
Chemical Name:
Paroxetine hydrochloride
Synonyms
PAROXETINE HCL;Paroxetine Hydrochloride RS;Paroxetine hydrochloride,trans-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine hydrochloride;FG-7051;Deroxat;Seroxat;brl29060a;BRL-29060;(3s,4r)-orid;BRL29060 HCl
CBNumber:
CB8178022
Molecular Formula:
C19H21ClFNO3
Molecular Weight:
365.83
MDL Number:
MFCD00797405
MOL File:
78246-49-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41
Product description Number Pack Size Price
Paroxetine hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard Y0000578 70 mg $167
Paroxetine hydrochloride United States Pharmacopeia (USP) Reference Standard 1500218 350mg $425
Paroxetine hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard Y0000578 y0000578 $153
Paroxetine (hydrochloride) ≥98% 14998 10mg $54
Paroxetine (hydrochloride) ≥98% 14998 25mg $127
More product size

Paroxetine hydrochloride Properties

Melting point 129-131°C
storage temp. 2-8°C
solubility insoluble in H2O; ≥17.8 mg/mL in EtOH; ≥18.29 mg/mL in DMSO
form Solid
color White to off-white
Major Application pharmaceutical (small molecule)
InChI InChI=1/C19H20FNO3.ClH/c20-15-3-1-13(2-4-15)17-7-8-21-10-14(17)11-22-16-5-6-18-19(9-16)24-12-23-18;/h1-6,9,14,17,21H,7-8,10-12H2;1H/t14-,17-;/s3
InChIKey GELRVIPPMNMYGS-ZXIWTAKENA-N
SMILES N1CC[C@@H](C2=CC=C(F)C=C2)[C@H](COC2=CC=C3OCOC3=C2)C1.[H]Cl |&1:3,11,r|
CAS DataBase Reference 78246-49-8(CAS DataBase Reference)
NCI Dictionary of Cancer Terms paroxetine hydrochloride
FDA UNII 3I3T11UD2S
NCI Drug Dictionary paroxetine hydrochloride
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
RIDADR  3249
HazardClass  6.1(b)
PackingGroup  III
HS Code  29339900
NFPA 704
0
3 0

Paroxetine hydrochloride price More Price(83)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000578 Paroxetine hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard 78246-49-8 70 mg $167 2026-04-30 Buy
Sigma-Aldrich 1500218 Paroxetine hydrochloride United States Pharmacopeia (USP) Reference Standard 78246-49-8 350mg $425 2025-07-31 Buy
Sigma-Aldrich Y0000578 Paroxetine hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard 78246-49-8 y0000578 $153 2024-03-01 Buy
Cayman Chemical 14998 Paroxetine (hydrochloride) ≥98% 78246-49-8 10mg $54 2026-04-30 Buy
Cayman Chemical 14998 Paroxetine (hydrochloride) ≥98% 78246-49-8 25mg $127 2026-04-30 Buy
Product number Packaging Price Buy
Y0000578 70 mg $167 Buy
1500218 350mg $425 Buy
Y0000578 y0000578 $153 Buy
14998 10mg $54 Buy
14998 25mg $127 Buy

Paroxetine hydrochloride Chemical Properties,Uses,Production

Chemical Properties

White Crystalline Powder

Originator

Paxil, SmithKline Beecham ,France

Uses

Paroxetine is an antidepressant drug of the SSRI type

Uses

A selective serotonin reuptake inhibitor. Used as an antidepressant

Definition

ChEBI: Paroxetine hydrochloride is the hydrochloride salt of paroxetine. It is an antidepressant drug. It has a role as an antidepressant, an anxiolytic drug, a hepatotoxic agent, a P450 inhibitor and a serotonin uptake inhibitor. It contains a paroxetinium(1+).

Manufacturing Process

251 g of methyl-4-(4-fluorophenyl)-N-methyl-nipecotinate, 8 g of sodium methoxide and 500 ml benzene were refluxed for 2 h. The benzene solution was washed with cold water and evaporated to give the pure α-ester which was dissolved in a mixture of 320 ml of water and 450 ml concentrated hydrochloric acid. The solution was slowly distilled to remove methanol and finally evaporated to dryness in vacuo.
400 ml thionyl chloride were added in small portions to the solid. The mixture was allowed to stand for 3 h at room temperature and was then evaporated to dryness in vacuo with tetrachloroethane giving methyl-4-(4-fluorophenyl)-Nmethylnipecotic acid chloride. The acid chloride was added in small portions to a solution of 160 g (-)-menthol in 800 ml pyridine at a temperature of 0°-5°C. The mixture was allowed to stand at room temperature to the next day. Ice water and 50% sodium hydroxide were added, and the mixture was extracted with ether. The ether was dried with anhydrous magnesium sulphate, filtered and evaporated. Distillation in vacuo gave the menthol ester in a yield of 7580%. Boiling point at 0.05 mm Hg was 165°-170°C.
Racemic 4-(4-fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine (50 g) was dissolved in a mixture of 21.6 ml of concentrated sulfuric acid and 50 ml of water. To the solution were added 25 ml of concentrated hydrochloric acid and 22.4 ml of 37% formaldehyde solution. The mixture was refluxed for 5 h, cooled, and 125 ml of concentrated ammonia were added. The mixture was extracted with 50 ml of toluene. Drying of the toluene solution and distillation gave 38 g of 4-(4-fluorophenyl)-3-hydroxymethyl-1-methyl-1,2,3,6tetrahydropyridine with boiling point 110°-120°C at 0.1 mm Hg.
13 g of the racemic compound and 22 g of (-)-dibenzoyltartaric acid were dissolved in 105 ml of hot methanol. On cooling, 9 g of salt of (-)-4-(4fluorophenyl)-3-hydroxymethyl-1-methyl-1,2,3,6-tetrahydropyridine crystallized. Melting point 167°-168°C.
38 g of (-)-4-(4-fluorophenyl)-3-hydroxymethyl-1-methyl-1,2,3,6tetrahydropyridine were dissolved in 350 ml of 99% ethanol, 5 g of 5% palladium on carbon were added, and the mixture was treated with hydrogen until 4500 ml were absorbed. The catalyst was filtered off, and the solution was evaporated to yield 37.5 g of (+)-b-4-(4-fluorophenyl)-3-hydroxymethyl1-methylpiperidine.
To a solution of sodium in methanol (125 ml) were added 3,4methylenedioxyphenol (29 g) and the (+)-b-4-(4-fluorophenyl)-3hydroxymethyl-1-methylpiperidine (37,5 g). The mixture was stirred and refluxed. After removal of the solvent in vacuo, the evaporation residue was poured into a mixture of ice (150 g), water (150 ml), and ether (200 ml). The ether layer was separated, and the aqueous layer was extracted with ether. The combined ether solutions were washed with water and dried with anhydrous magnesium sulphate, and the ether was evaporated. The residue was triturated with 200 ml of 99% ethanol and 11.5 ml of concentrated hydrochloric acid, yielding 30 g of (-)-b-4-(4-fluorophenyl-3-(1,3-benzdioxolyl(3)-oxymethyl)-1-methylpiperidine, hydrochloride were obtained. Melting point 202°C.

brand name

Paxil (GlaxoSmithKline).

Therapeutic Function

Antidepressant

Biological Activity

paroxetine hydrochloride is a antidepressant agents known as selective serotonin-reuptake inhibitors (ssris).paroxetine is a potent and highly selective inhibitor of neuronal serotonin reuptake. paroxetine likely inhibits the reuptake of serotonin at the

storage

Room temperature

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View Lastest Price from Paroxetine hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Paroxetine hydrochloride pictures 2026-08-08 Paroxetine hydrochloride
78246-49-8
0.99 RongNa Biotechnology Co.,Ltd
Paroxetine Hydrochloride pictures 2026-08-07 Paroxetine Hydrochloride
78246-49-8
2Kg/Bag EP 20 tons Sinoway Industrial co., ltd.
Paroxetine hydrochloride pictures 2026-07-27 Paroxetine hydrochloride
78246-49-8
$34.00-153.00 99.87% 10g TargetMol Chemicals Inc.

Paroxetine hydrochloride Spectrum

PAROMOMYCINSULFATE (3s,4r)-orid (3s-trans)-id 3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-,hydrochloride,(3s-trans)-piperidin 3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-piperidinhydrochl PAROXETINE HC (3S,4R)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)-piperidine hydrochloride hemihydrate 5-[[(3S,4R)-4-(4-Fluorophenyl)-3-piperidyl]methoxy]-1,3-benzodioxole·hydrochloride 3-[(1,3-benzodioxol-5-yloxy)meth Paroetine Hydrochloride HeMihydrate (3S,4R)-3-((Benzo[d][1,3]dioxol-5-yloxy)Methyl)-4-(4-fluorophenyl)piperidine hydrochloride Paroxetine HCl heMihydrate API Proxetine Hydrochloride Paroxetine HCl Anhydrous (3S,4R)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)-piperidine, hydrochloride (1:1) Paroxetine HCL USP37 Paroxetine hydrochloride, 99%, a selective serotonin-reuptake inhibitor BRL29060 HYDROCHLORIDE;BRL29060A 3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-piperidinhydrochlor brl29060a brl29060hydrochloride BRL-29060 FG-7051 (3S-TRANS)-3-[(1,3-BENZODIOXOL-5-YLOXY)METHYL]-4-(4-FLUOROPHENYL)PIPERIDINE (3s-trans)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine hydrochloride PAROXETINE HYDROCHLORIDE PAROXETIN X HCL (-)TRANS-3-[(1,3-BENZODIOXOL-5-YLOXY) METHYL]-4-(4-FLUOROPHENYL) PAROXETINE HYDROCHLORIDE Paroxetine HCL EP4.5 Paroxeting chlorhydric acid ParoxetineHCl.1/2H2O (-)TRANS-3-[(1,3-BENZODIOXOL-5-YLOXY)METHYL]-4-(4-FLUOROPHENYL)PIPERIDINE HYDROCHLORIDE Deroxat Seroxat Piperidine, 3-(1,3-benzodioxol-5-yloxy)methyl-4-(4-fluorophenyl)-, hydrochloride, (3S,4R)- Paroxetine hydrochloride hemihydrate CRS Paroxetine hydrochloride USP/EP/BP Paroxetine HCl (BRL29060) Paroxetine hydrochlorideQ: What is Paroxetine hydrochloride Q: What is the CAS Number of Paroxetine hydrochloride Q: What is the storage condition of Paroxetine hydrochloride Q: What are the applications of Paroxetine hydrochloride Paroxetine D6 HydrochlorideQ: What is Paroxetine D6 Hydrochloride Q: What is the CAS Number of Paroxetine D6 Hydrochloride Q: What is the storage condition of Paroxetine D6 Hydrochloride Q: What are the applications of Paroxetine D6 Hydrochloride TIANFU-CHEM CAS:78246-49-8 Paroxetine hydrochloride Paroxetine Hydrochloride EP Standard (3S,4R)-3-[(2H-1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine hydrochloride Paxil hydrochloride BRL29060 HCl Paroxetine hydrochloride, 10 mM in DMSO Paroxetine hydrochloride (BRL29060 hydrochloride Paroxetine hydrochloride,trans-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine hydrochloride PAROXETINE HCL Paroxetine Hydrochloride RS 78246-49-8 C19H20NO3FHCl C19H20FNO3ClH C19H21ClFNO3 C19H20FNO3HClC19H21ClFNO3 C20H21FNO3 C19H20FNO3HCl Csub1subsub9subHsub2subsub0subFNOsub3subHCl