Hydroxy Ebastine

Base Information

Chemical Name:Hydroxy Ebastine
CAS No.:210686-41-2
Molecular Formula:C32H39 N O3
Molecular Weight:485.667
Hs Code.:
UNII:U07WX9MN7J
DSSTox Substance ID:DTXSID40475394
Nikkaji Number:J972.078B
Wikidata:Q82305902
Mol file:210686-41-2.mol

Synonyms:hydroxyebastine

Suppliers and Price of Hydroxy Ebastine

Supply Marketing:

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

Usbiological
Hydroxy Ebastine
1mg
$ 460.00

TRC
HydroxyEbastine
1mg
$ 185.00

Medical Isotopes, Inc.
HydroxyEbastine
1 mg
$ 890.00

Medical Isotopes, Inc.
HydroxyEbastine
5 mg
$ 2120.00

Cayman Chemical
Hydroxy Ebastine ≥87%
1mg
$ 161.00

Cayman Chemical
Hydroxy Ebastine ≥87%
500μg
$ 85.00

American Custom Chemicals Corporation
HYDROXY EBASTINE 95.00%
10MG
$ 1871.10

AK Scientific
HydroxyEbastine
1mg
$ 299.00

Total 7 raw suppliers

Chemical Property of Hydroxy Ebastine

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:53-55°C
Refractive Index:1.603
Boiling Point:632.848°C at 760 mmHg
Flash Point:336.535°C
PSA：49.77000
Density:1.141g/cm³
LogP:6.12790
Storage Temp.:-20°C Freezer
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:485.29299411
Heavy Atom Count:36
Complexity:618

Purity/Quality:

> 95% ^*data from raw suppliers

Hydroxy Ebastine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(CO)C1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)OC(C3=CC=CC=C3)C4=CC=CC=C4
Uses A metabolite of Ebastine A metabolite of Ebastine.

Technology Process of Hydroxy Ebastine

There total 1 articles about Hydroxy Ebastine 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: 63.0%

: 90729-43-4
ebastine

: 210686-41-2
Hydroxyebastine

Guidance literature:: With Streptomyces platensis NRRL 2364; In N,N-dimethyl-formamide; at 30 ℃; for 16h; pH=5; aq. buffer; Microbiological reaction;
DOI:10.1016/j.tet.2008.09.098