(R,S)-Palonosetron Hydrochloride

Base Information Edit

Chemical Name:(R,S)-Palonosetron Hydrochloride
CAS No.:135755-51-0
Molecular Formula:C19H25ClN2O
Molecular Weight:332.8676
Hs Code.:2933790002
Mol file:135755-51-0.mol

Synonyms:Palonosetron hydrochloride;Aloxi;

Suppliers and Price of (R,S)-Palonosetron Hydrochloride

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(R,S)-PalonosetronHydrochloride(90%)
25mg
$ 2310.00

Crysdot
(R)-2-((1R,3S,4R)-Quinuclidin-3-yl)-2,3,3a,4,5,6-hexahydro-1H-benzo[de]isoquinolin-1-onehydrochloride 97%
1g
$ 1131.00

American Custom Chemicals Corporation
(R,S)-PALONOSETRON HYDROCHLORIDE 95.00%
5MG
$ 759.00

Total 30 raw suppliers

Chemical Property of (R,S)-Palonosetron Hydrochloride Edit

Chemical Property:

Melting Point:>197°C (dec.)
PSA：23.55000
LogP:3.33430
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly), Water (Sparingly)

Purity/Quality:

99% ^*data from raw suppliers

(R,S)-PalonosetronHydrochloride(90%) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses The (R,S)-enantiomer of Palonosetron (P165800), a potent and selective antagonist, with 5-HT3 receptor The (R,S)-enantiomer of Palonosetron (P165800), a potent and selective antagonist, with 5-HT3 receptor in vitro. An impurity of Palonosetron.

Technology Process of (R,S)-Palonosetron Hydrochloride

There total 38 articles about (R,S)-Palonosetron Hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.72%