Schizanthine G

Schizanthine G
Product Name Schizanthine G
CAS No.: 119736-74-2
Catalog No.: CFN00224
Molecular Formula: C19H27NO6
Molecular Weight: 365.42 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: The herbs of Schizanthus pinnatus Ruiz et Pav.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Schizanthine G is a natural product from Schizanthus pinnatus Ruiz et Pav.
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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.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2019, 1124:323-330
  • Neurochem Res.2021, s11064-021-03449-0
  • Vietnam Journal of Food Control.2022, 5(2): 115-128.
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  • Nutrients.2020, 12(11):3448.
  • Mol Divers.2022, s11030-022-10586-3.
  • Molecules.2021, 26(16):4722.
  • Phytomedicine Plus2022, 2(1):100207.
  • Evid Based Complement Alternat Med.2020, 2020:1970349.
  • Processes2021, 9(1), 153;
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    Heterocycles,1988 ,27(8) :1887-97.
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    METHODS AND RESULTS:
    From Schizanthus pinnatus Ruiz et Pav. we have isolated seven new tropan-3α,6β-diol diesters, schizanthine F (1), Schizanthine G (2), schizanthine H (3), schizanthine I (4), schizanthine K. (8), schizanthine L (9), and schizanthine M (10), together with tropine, (-) -6β-angeloyloxytropan-3α-ol (5), (-)-6β-tigloyloxytropan-3α-ol (6), and (-)-3α-senecioyloxytropan-6β-ol (7).
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    The structures of the new alkaloids were determined mainly by spectroscopia methods comprising 2-D and 1-D nmr long-range heteronuclear correlations.
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