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rac-Paroxetine-d4 Hydrochloride

CAS No.
2714485-95-5
Chemical Name:
rac-Paroxetine-d4 Hydrochloride
Synonyms
rac-Paxil-d4;rac-Aropax-d4;rac-Deroxat-d4;rac-Seroxat-d4;D4-Paroxetine HCl;rel-Paroxetine (hydrochloride);rac-3-[(1,3-Benzod-d4-ioxol-5-yloxy)methyl]-4-(4-fluorophenyl-d4)piperidine Hydrochloride;(3S,4R)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(2,3,5,6-tetradeuterio-4-fluorophenyl)piperidine
CBNumber:
CB413162540
Molecular Formula:
C19H16D4FNO3.ClH
Molecular Weight:
369.85
MDL Number:
MOL File:
2714485-95-5.mol
MSDS File:
SDS
Last updated:2026-05-11 19:39:08

rac-Paroxetine-d4 Hydrochloride Properties

form Solid
color White to off-white

rac-Paroxetine-d4 Hydrochloride price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0378840 Paroxetine-d4 hydrochloride 99.16% 2714485-95-5 1mg $487 2026-06-04 Buy
aablocks AA029Y4M Paroxetine-d4 (hydrochloride) >98% 2714485-95-5 1mg $535 2026-06-02 Buy
Product number Packaging Price Buy
CS-0378840 1mg $487 Buy
AA029Y4M 1mg $535 Buy

rac-Paroxetine-d4 Hydrochloride Chemical Properties, Uses, Production

Uses

Paroxetine-d4 (hydrochloride) is deuterium labeled Paroxetine (hydrochloride). Paroxetine hydrochloride is a potent selective serotonin-reuptake inhibitor, commonly prescribed as an and has GRK2 inhibitory ability with IC50 of 14μM. Paroxetine hydrochloride can be used for the research of depressive disorder[1][2][3].

References

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Liu RP, et al. Paroxetine ameliorates lipopolysaccharide-induced microglia activation via differential regulation of MAPK signaling. J Neuroinflammation. 2014 Mar 12;11:47. DOI:10.1186/1742-2094-11-47
[3] Wang Q, et al. Paroxetine alleviates T lymphocyte activation and infiltration to joints of collagen-induced arthritis. Sci Rep. 2017 Mar 28;7:45364. DOI:10.1038/srep45364
[4] Lassen TR, et al. Effect of paroxetine on left ventricular remodeling in an in vivo rat model of myocardial infarction. Basic Res Cardiol. 2017 May;112(3):26. DOI:10.1007/s00395-017-0614-5
[5] Zarei M, et al. Paroxetine attenuates the development and existing pain in a rat model of neurophatic pain. Iran Biomed J. 2014;18(2):94-100. DOI:10.6091/ibj.1282.2013
[6] Waldschmidt HV, et al. Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine. J Med Chem. 2017 Apr 13;60(7):3052-3069. DOI:10.1021/acs.jmedchem.7b00112

rac-Paroxetine-d4 Hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

rac-Paroxetine-d4 Hydrochloride Suppliers

Global Suppliers ( 5)
Supplier Tel Email Country ProdList Advantage
Cato Research Chemicals Inc. 020-81960175-877 18933936954 tianwen.zhan@cato-chem.com China 7335 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29874 58
ShangHai ZskBio CO., LTD 021-58056897 15399714481 info@zsklab.com China 7539 58
TLC Pharmaceutical Standards Ltd. 18012923235 chinasales04@tlcstandards.com.cn China 8143 58
TargetMol Chemicals Inc. 13564774135 marketing@targetmol.com United States 19950 58

View Latest Price from rac-Paroxetine-d4 Hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Paroxetine-D4 hydrochloride pictures 2026-05-11 Paroxetine-D4 hydrochloride
2714485-95-5
10g TargetMol Chemicals Inc.
(3S,4R)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(2,3,5,6-tetradeuterio-4-fluorophenyl)piperidine rac-3-[(1,3-Benzod-d4-ioxol-5-yloxy)methyl]-4-(4-fluorophenyl-d4)piperidine Hydrochloride rac-Aropax-d4 rac-Deroxat-d4 rac-Paxil-d4 rac-Seroxat-d4 rel-Paroxetine (hydrochloride) D4-Paroxetine HCl 2714485-95-5