Merucathine

CAS# 107673-74-5

Merucathine

Catalog No. BCN1782----Order now to get a substantial discount!

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Quality Control of Merucathine

Number of papers citing our products

Chemical structure

Merucathine

3D structure

Chemical Properties of Merucathine

Cas No. 107673-74-5 SDF Download SDF
PubChem ID 5459034 Appearance Needles
Formula C11H15NO M.Wt 177.25
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (E,3R,4S)-4-amino-1-phenylpent-1-en-3-ol
SMILES CC(C(C=CC1=CC=CC=C1)O)N
Standard InChIKey MSCXFOZFDVCLHC-PRXIFDQHSA-N
Standard InChI InChI=1S/C11H15NO/c1-9(12)11(13)8-7-10-5-3-2-4-6-10/h2-9,11,13H,12H2,1H3/b8-7+/t9-,11+/m0/s1
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 Merucathine

The herbs of Catha edulis

Biological Activity of Merucathine

In vitro

Chiral resolution of cationic drugs of forensic interest by capillary electrophoresis with mixtures of neutral and anionic cyclodextrins.[Pubmed: 7810901]

Anal Chem. 1994 Nov 15;66(22):4019-26.


METHODS AND RESULTS:
Chiral resolution of a number of cationic drugs of forensic interest (amphetamine, methamphetamine, cathinone, methcathinone, cathine, cocaine, propoxyphene, and various alpha-hydroxyphenethylamines) is achieved via capillary electrophoresis (CE) with added cyclodextrins (CDs), including novel mixtures of neutral and anionic CDs. In the latter studies, resolution and migration speed are readily adjusted by varying the ratio of the two added CDs, as the anionic CD acts as a counter-migrating complexing reagent. The neutral CD, heptakis(2,6-di-O-methyl)-beta-CD, was found suitable for the analysis of illicit cocaine and khat leaves (Catha edulis Forsk), which contain (-)-alpha-aminopropiophenone ((-)-cathinone), (+)-norpseudoephedrine (cathine), (-)-norephedrine, and trace levels of the phenylpentenylamines (+)-merucathinone, (+)-Merucathine, and possibly (-)-pseudoMerucathine.
CONCLUSIONS:
The use of mixtures of the neutral and the anionic CD (beta-CD sulfobutyl ether IV) was found suitable for the analysis of illicit amphetamine, methamphetamine, methcathinone, and propoxyphene. A model is presented for the impact of mixtures of neutral and anionic CDs on migration behavior and chiral resolution in CE.

Merucathine Dilution Calculator

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Merucathine Molarity Calculator

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Preparing Stock Solutions of Merucathine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.6417 mL 28.2087 mL 56.4175 mL 112.835 mL 141.0437 mL
5 mM 1.1283 mL 5.6417 mL 11.2835 mL 22.567 mL 28.2087 mL
10 mM 0.5642 mL 2.8209 mL 5.6417 mL 11.2835 mL 14.1044 mL
50 mM 0.1128 mL 0.5642 mL 1.1283 mL 2.2567 mL 2.8209 mL
100 mM 0.0564 mL 0.2821 mL 0.5642 mL 1.1283 mL 1.4104 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.

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References on Merucathine

Chiral resolution of cationic drugs of forensic interest by capillary electrophoresis with mixtures of neutral and anionic cyclodextrins.[Pubmed:7810901]

Anal Chem. 1994 Nov 15;66(22):4019-26.

Chiral resolution of a number of cationic drugs of forensic interest (amphetamine, methamphetamine, cathinone, methcathinone, cathine, cocaine, propoxyphene, and various alpha-hydroxyphenethylamines) is achieved via capillary electrophoresis (CE) with added cyclodextrins (CDs), including novel mixtures of neutral and anionic CDs. In the latter studies, resolution and migration speed are readily adjusted by varying the ratio of the two added CDs, as the anionic CD acts as a counter-migrating complexing reagent. The neutral CD, heptakis(2,6-di-O-methyl)-beta-CD, was found suitable for the analysis of illicit cocaine and khat leaves (Catha edulis Forsk), which contain (-)-alpha-aminopropiophenone ((-)-cathinone), (+)-norpseudoephedrine (cathine), (-)-norephedrine, and trace levels of the phenylpentenylamines (+)-merucathinone, (+)-Merucathine, and possibly (-)-pseudoMerucathine. The use of mixtures of the neutral and the anionic CD (beta-CD sulfobutyl ether IV) was found suitable for the analysis of illicit amphetamine, methamphetamine, methcathinone, and propoxyphene. A model is presented for the impact of mixtures of neutral and anionic CDs on migration behavior and chiral resolution in CE.

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