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Nortropacocaine

CAS# 18470-33-2

Nortropacocaine

Catalog No. BCN1889----Order now to get a substantial discount!

Product Name & Size Price Stock
Nortropacocaine:5mg Please Inquire In Stock
Nortropacocaine:10mg Please Inquire In Stock
Nortropacocaine:20mg Please Inquire In Stock
Nortropacocaine:50mg Please Inquire In Stock

Quality Control of Nortropacocaine

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Chemical structure

Nortropacocaine

3D structure

Chemical Properties of Nortropacocaine

Cas No. 18470-33-2 SDF Download SDF
PubChem ID 192953 Appearance Cryst.
Formula C14H17NO2 M.Wt 231.29
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-(8-azabicyclo[3.2.1]octan-3-yl)benzoic acid
SMILES C1CC2CC(CC1N2)C3=CC=CC(=C3)C(=O)O
Standard InChIKey HRTCUJBTNCFSIO-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H17NO2/c16-14(17)10-3-1-2-9(6-10)11-7-12-4-5-13(8-11)15-12/h1-3,6,11-13,15H,4-5,7-8H2,(H,16,17)
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.

Protocol of Nortropacocaine

Structure Identification
J Pharm Sci. 1979 Jun;68(6):788-90.

Nortropacocaine hydrochloride conformation in aqueous and hydrophobic media.[Pubmed: 458585]

The Nortropacocaine hydrochloride PMR spectra in deuterium oxide and in deuterochloroform differed markedly.
METHODS AND RESULTS:
A detailed conformational analysis using vicinal 1H-1H coupling constants revealed the molecular conformation to be identical in both solvents. The preferred conformation was one in which the piperidine component existed as a deformed chair. The spectral differences were due to a decreased deshielding of the protonated nitrogen on the neighboring bicyclic ring protons, resulting in chemical shift changes.

Nortropacocaine Dilution Calculator

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Nortropacocaine Molarity Calculator

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Preparing Stock Solutions of Nortropacocaine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.3236 mL 21.6179 mL 43.2358 mL 86.4715 mL 108.0894 mL
5 mM 0.8647 mL 4.3236 mL 8.6472 mL 17.2943 mL 21.6179 mL
10 mM 0.4324 mL 2.1618 mL 4.3236 mL 8.6472 mL 10.8089 mL
50 mM 0.0865 mL 0.4324 mL 0.8647 mL 1.7294 mL 2.1618 mL
100 mM 0.0432 mL 0.2162 mL 0.4324 mL 0.8647 mL 1.0809 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 Nortropacocaine

Nortropacocaine hydrochloride conformation in aqueous and hydrophobic media.[Pubmed:458585]

J Pharm Sci. 1979 Jun;68(6):788-90.

The Nortropacocaine hydrochloride PMR spectra in deuterium oxide and in deuterochloroform differed markedly. A detailed conformational analysis using vicinal 1H-1H coupling constants revealed the molecular conformation to be identical in both solvents. The preferred conformation was one in which the piperidine component existed as a deformed chair. The spectral differences were due to a decreased deshielding of the protonated nitrogen on the neighboring bicyclic ring protons, resulting in chemical shift changes.

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