Metiprenaline

Base Information

Chemical Name:Metiprenaline
CAS No.:1212-03-9
Molecular Formula:C12H19 N O3
Molecular Weight:225.288
Hs Code.:2922509090
UNII:1WBF92D66N
DSSTox Substance ID:DTXSID20862602
Nikkaji Number:J7.457H
Wikidata:Q27252989
NCI Thesaurus Code:C87676
ChEMBL ID:CHEMBL2074647
Mol file:1212-03-9.mol

Synonyms:3-O-methoxyisoprenaline;3-O-methylisoprenaline sulfate;metiprenaline;metiprenaline hydrochloride;metiprenaline sulfate;O-methylisoprenaline

Suppliers and Price of Metiprenaline

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
Metiprenaline
10mg
$ 531.00

TRC
Metiprenaline
25mg
$ 485.00

American Custom Chemicals Corporation
METIPRENALINE 95.00%
5MG
$ 495.41

Total 6 raw suppliers

Chemical Property of Metiprenaline

Chemical Property:

Vapor Pressure:7.03E-07mmHg at 25°C
Boiling Point:392.9°Cat760mmHg
Flash Point:191.4°C
PSA：61.72000
Density:1.117g/cm³
LogP:1.82310
XLogP3:-0.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:225.13649347
Heavy Atom Count:16
Complexity:199

Purity/Quality:

99% ^*data from raw suppliers

Metiprenaline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NCC(C1=CC(=C(C=C1)O)OC)O
Uses Metiprenaline is a derivative of normetadrenaline, a metabolite most commonly found in urine. High levels of normetadrenaline in the urine indicate the possibility of having pheochromocytoma, a condition where catecholamineproducing tumours arise from chromaffin cells.

Technology Process of Metiprenaline

There total 2 articles about Metiprenaline 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:

: 91644-72-3
1-(4-hydroxy-3-methoxy-phenyl)-2-isopropylamino-ethanone; hydrochloride

: 1212-03-9
3-O-methylisoproterenol

Guidance literature:: With palladium on activated charcoal; ethanol; Hydrogenation;

Reference yield:

: 1212-03-9
3-O-methylisoproterenol

Guidance literature:: 4-Hydroxy-ω-isopropylamino-3-methoxy-acetophenon, Hydrierung an Raney-Nickel in A., 45grad 2at; Isolierung als Hydrochlorid;