Home >> Research Area >>Natural Products>>Alkaloids>> N-Methylcorydiniumiodide

N-Methylcorydiniumiodide

CAS# 4668-64-6

N-Methylcorydiniumiodide

Catalog No. BCN7873----Order now to get a substantial discount!

Product Name & Size Price Stock
N-Methylcorydiniumiodide: 5mg Please Inquire In Stock
N-Methylcorydiniumiodide: 10mg Please Inquire In Stock
N-Methylcorydiniumiodide: 20mg Please Inquire Please Inquire
N-Methylcorydiniumiodide: 50mg Please Inquire Please Inquire
N-Methylcorydiniumiodide: 100mg Please Inquire Please Inquire
N-Methylcorydiniumiodide: 200mg Please Inquire Please Inquire
N-Methylcorydiniumiodide: 500mg Please Inquire Please Inquire
N-Methylcorydiniumiodide: 1000mg Please Inquire Please Inquire

Quality Control of N-Methylcorydiniumiodide

Number of papers citing our products

Chemical structure

N-Methylcorydiniumiodide

Chemical Properties of N-Methylcorydiniumiodide

Cas No. 4668-64-6 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C21H26NO4 M.Wt 356.43
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of N-Methylcorydiniumiodide

The flower of Magnolia liliiflora

Biological Activity of N-Methylcorydiniumiodide

DescriptionN-Methylcorydinium iodide is a natural product from Glaucium oxylobum BOISS. et BUSHE.

Protocol of N-Methylcorydiniumiodide

Structure Identification
Collect. Czech. Chem. Commun. 1985, 50, 854-860.

Quaternary alkaloids from Glaucium oxylobum BOISS. et BUSHE.[Reference: WebLink]


METHODS AND RESULTS:
From the fraction of quaternary alkaloids of the aerial part of Glaucium oxylobum BOISS. et BUSHE (-)-trans-N-rnethylcanadinium iodide was isolated as the main alkaloid after conversion to iodides, and, in a smaller amount, (+)-N-Methylcorydinium iodide, detected for the first time in Papaveraceae, further (-)-trans-N-methylstylopinium iodide, magnoflorine iodide and a new quaternary alkaloid, N-methyldomesticinium iodide, isolated for the first time as a natural substance. In the roots, magnoflorine iodide accompanied by (+)-N-Methylcorydinium iodide represented the main component of the quaternary fraction. From both plant parts corytuberine was also isolated for the first time.
CONCLUSIONS:
In the tertiary fraction of alkaloids (+)-corydine, protopine and allocryptopine were the major components, accompanied by smaller amounts of sanguinarine, chelerythrine, chelirubine, domesticine, isoboldine and scoulerine. In the fraction of quaternary protoberberines coptisine, berberine and traces of corysamine were detected.

N-Methylcorydiniumiodide Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

N-Methylcorydiniumiodide Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of N-Methylcorydiniumiodide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.8056 mL 14.028 mL 28.056 mL 56.112 mL 70.14 mL
5 mM 0.5611 mL 2.8056 mL 5.6112 mL 11.2224 mL 14.028 mL
10 mM 0.2806 mL 1.4028 mL 2.8056 mL 5.6112 mL 7.014 mL
50 mM 0.0561 mL 0.2806 mL 0.5611 mL 1.1222 mL 1.4028 mL
100 mM 0.0281 mL 0.1403 mL 0.2806 mL 0.5611 mL 0.7014 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

University of Maryland School of Medicine

University of Illinois at Chicago

The Ohio State University

University of Zurich

Harvard University

Colorado State University

Auburn University

Yale University

Worcester Polytechnic Institute

Washington State University

Stanford University

University of Leipzig

Universidade da Beira Interior

The Institute of Cancer Research

Heidelberg University

University of Amsterdam

University of Auckland
TsingHua University
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on N-Methylcorydiniumiodide

Quaternary alkaloids from Glaucium oxylobum BOISS. et BUSHE.

Collect. Czech. Chem. Commun. 1985, 50, 854-860.

From the fraction of quaternary alkaloids of the aerial part of Glaucium oxylobum BOISS. et BUSHE (-)-trans-N-rnethylcanadinium iodide was isolated as the main alkaloid after conversion to iodides, and, in a smaller amount, (+)-N-Methylcorydinium iodide, detected for the first time in Papaveraceae, further (-)-trans-N-methylstylopinium iodide, magnoflorine iodide and a new quaternary alkaloid, N-methyldomesticinium iodide, isolated for the first time as a natural substance. In the roots, magnoflorine iodide accompanied by (+)-N-Methylcorydinium iodide represented the main component of the quaternary fraction. From both plant parts corytuberine was also isolated for the first time. In the tertiary fraction of alkaloids (+)-corydine, protopine and allocryptopine were the major components, accompanied by smaller amounts of sanguinarine, chelerythrine, chelirubine, domesticine, isoboldine and scoulerine. In the fraction of quaternary protoberberines coptisine, berberine and traces of corysamine were detected.

Keywords:

N-Methylcorydiniumiodide,4668-64-6,Natural Products, buy N-Methylcorydiniumiodide , N-Methylcorydiniumiodide supplier , purchase N-Methylcorydiniumiodide , N-Methylcorydiniumiodide cost , N-Methylcorydiniumiodide manufacturer , order N-Methylcorydiniumiodide , high purity N-Methylcorydiniumiodide

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: