Nortropacocaine

Nortropacocaine
Product Name Nortropacocaine
CAS No.: 18470-33-2
Catalog No.: CFN00171
Molecular Formula: C14H17NO2
Molecular Weight: 231.29 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Helicia lobata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Reference standards.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Chinese Pharmacological Bulletin2019, 35(8):1120-1125
  • Processes2021, 9(1), 153.
  • Mol Microbiol.2019, 112(1):317-332
  • Antimicrob Agents Chemother.2020, AAC.01921-20.
  • Int J Mol Sci.2019, 20(8):E1855
  • Phytofrontiers2024, 2690-5442.
  • Cell Biochem Funct.2018, 36(6):303-311
  • VNU Journal of Science2023, No. 20.
  • J Nat Sc Biol Med2019, 10(2):149-156
  • Int J Mol Sci.2018, 19(2)
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    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.
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