1-Methoxyallocryptopine

1-Methoxyallocryptopine
Product Name 1-Methoxyallocryptopine
CAS No.: 56743-52-3
Catalog No.: CFN89163
Molecular Formula: C22H25NO6
Molecular Weight: 399.44 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Turkish Papaver curviscapum.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
1-Methoxyallocryptopine is a natural product from Turkish Papaver curviscapum.
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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.
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  • Academic J of Second Military Medical University2018, 39(11)
  • Eur Rev Med Pharmacol Sci.2020, 24(9):5127-5139.
  • Int J Mol Sci.2019, 20(16):E4015
  • Korean Journal of Pharmacognosy2018, 49(3):270-277
  • Int J Mol Med.2016, 37(2):501-8
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  • Plant Physiol Biochem.2023, 202:107913.
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    Journal of Natural Products, 1983, 46(2):251-255.
    The Stereochemistry and 13 C Nmr Spectra of Protopinium Salts.[Reference: WebLink]

    METHODS AND RESULTS:
    The 13C nmr spectra for protopine (1), allocryptopine (4), 1-Methoxyallocryptopine (5), hunnemanine (6), and thalictricine (7), were recorded in TFA-d solution. There is a predominance of the cis protopinium salt over the trans isomer, except in the case of thalictricine where the trans salt is the major isomer.
    CONCLUSIONS:
    The chemical shifts of C-6, C-13 and the N-methyl group are particularly diagnostic of the stereochemistry of the protopinium salts.
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