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324817

Sigma-Aldrich

Acide (Aminométhyl)phosphonique

99%

Synonyme(s) :

AMPA

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About This Item

Formule linéaire :
NH2CH2P(O)(OH)2
Numéro CAS:
Poids moléculaire :
111.04
Numéro Beilstein :
1701219
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pureté

99%

Forme

solid

Solubilité

water: soluble 50 mg/mL, clear, colorless

Chaîne SMILES 

NCP(O)(O)=O

InChI

1S/CH6NO3P/c2-1-6(3,4)5/h1-2H2,(H2,3,4,5)

Clé InChI

MGRVRXRGTBOSHW-UHFFFAOYSA-N

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Description générale

(Aminomethyl)phosphonic acid is a metabolite of amitrole and glyphosate herbicides and was analyzed by HPLC using an electrochemical detector.

Application

(Aminomethyl)phosphonic acid was used to develop a novel kind of immobilized metal affinity chromatography column based on organic-inorganic hybrid silica monolith.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Francisco Sánchez-Bayo et al.
Analytica chimica acta, 675(2), 125-131 (2010-08-31)
The herbicides amitrole and glyphosate, and its metabolite aminomethyl-phosphonic acid (AMPA), in water samples have been directly analysed by high-performance liquid chromatography using an electrochemical (EC) detector. Limits of detection of 0.3 microg mL(-1) for glyphosate, 0.05 microg mL(-1) for
Chunyan Hou et al.
Journal of proteome research, 9(8), 4093-4101 (2010-06-24)
A novel kind of immobilized metal affinity chromatography (IMAC) column based on organic-inorganic hybrid silica monolith has been developed. The monolithic support was prepared in a 250 microm i.d. capillary by the sol-gel method with tetraethoxysilane (TEOS) and 3-aminopropyltriethoxysilane (APTES)
M Tomita et al.
Journal of chromatography, 571(1-2), 324-330 (1991-11-15)
Capillary electrophoresis has been used to separate and quantitate glyphosate and its major metabolite, (aminomethyl)phosphonic acid (AMPA), in serum. The two compounds, after derivatization with p-toluenesulphonyl chloride, were clearly separated with 0.1 M boric acid-sodium hydroxide buffer (pH 9.6) containing
G M Williams et al.
Regulatory toxicology and pharmacology : RTP, 31(2 Pt 1), 117-165 (2000-06-15)
Reviews on the safety of glyphosate and Roundup herbicide that have been conducted by several regulatory agencies and scientific institutions worldwide have concluded that there is no indication of any human health concern. Nevertheless, questions regarding their safety are periodically
E Börjesson et al.
Journal of chromatography. A, 886(1-2), 207-216 (2000-08-19)
New methods were developed to determine glyphosate, N-(phosphonomethyl)glycine, and its major metabolite, (aminomethyl)phosphonic acid in groundwater and soil. The methods involve ligand-exchange, anion-exchange and derivatisation and final identification and quantification by GC-MS. The limits of quantification in this experiment were

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