2-(Methylamino)ethylphosphonic acid

2-(Methylamino)ethylphosphonic acid
Product Name 2-(Methylamino)ethylphosphonic acid
CAS No.: 14596-55-5
Catalog No.: CFN00033
Molecular Formula: C3H10NO3P
Molecular Weight: 139.09 g/mol
Purity: >=98%
Type of Compound: Miscellaneous
Physical Desc.: Powder
Source: From Anthopleura xanthogrammica
Solvent: DMSO, Pyridine, Methanol, Ethanol, 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.
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    Isolation and Characterization of the N-Methyl Derivatives of 2-Aminoethylphosphonic Acid from the Sea Anemone, Anthopleura xanthogrammica.[Reference: WebLink]

    METHODS AND RESULTS:
    The phosphonic acid analogs of choline phosphate (trimethyl-2-phosphonoethylammonium hydroxide inner salt) and 2-(Methylamino)ethylphosphonic acid have been isolated in crystalline form from the ethanolic extracts of the sea anemone, Anthopleura xanthogrammica. The presence of a small amount of 2-dimethylaminoethylphosphonic acid was also detected. The three N-methyl derivatives of 2-aminoethyl-phosphonic acid have been synthesized and the structures of the isolated phosphonic acids have been established by comparison with the synthetic compounds.
    CONCLUSIONS:
    The biological occurrence of the phosphonic acid analogs of ethanolamine phosphate, serine phosphate, and choline phosphate, the three major constituents of phospholipids, has now been established.
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