ATMP

For other uses, see ATMP (disambiguation).

ATMP
Names

IUPAC name [Bis(phosphonomethyl)amino]methylphosphonic acid
Other names Tris(phosphonomethyl)amine; Nitrilotrimethylphosphonic acid; Aminotris(methylphosphonic acid); ATMP; NTMP
Identifiers
CAS Number	6419-19-8^Y
ChEMBL	ChEMBL260191^Y
ChemSpider	15833^Y
EC Number	229-146-5
Jmol interactive 3D	Image
PubChem	16698
UNII	1Y702GD0FG^N
InChI InChI=1S/C3H12NO9P3/c5-14(6,7)1-4(2-15(8,9)10)3-16(11,12)13/h1-3H2,(H2,5,6,7)(H2,8,9,10)(H2,11,12,13)^Y Key: YDONNITUKPKTIG-UHFFFAOYSA-N^Y InChI=1/C3H12NO9P3/c5-14(6,7)1-4(2-15(8,9)10)3-16(11,12)13/h1-3H2,(H2,5,6,7)(H2,8,9,10)(H2,11,12,13) Key: YDONNITUKPKTIG-UHFFFAOYAN
SMILES O=P(O)(O)CN(CP(=O)(O)O)CP(=O)(O)O
Properties
Chemical formula	C₃H₁₂NO₉P₃
Molar mass	299.05 g·mol⁻¹
Appearance	White solid
Density	1.33 g/cm³ (20 °C)
Melting point	200 °C (392 °F; 473 K) decomposes
Solubility in water	61 g/100 mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

ATMP or aminotris(methylenephosphonic acid) is a phosphonic acid with chemical formula N(CH₂PO₃H₂)₃. It has chelating properties. It can be synthesized from the Mannich-type reaction of ammonia, formaldehyde, and phosphorous acid.^[1]

Properties

ATMP has better antiscale performance than that of polyphosphate through its excellent chelating ability, low threshold inhibition and lattice distortion process. It can prevent scale formation in water systems. ATMP is the phosphonate analog of nitrilotriacetic acid.

Applications

References

↑ Moedritzer, Kurt; Irani, Riyad R. (1966). "The Direct Synthesis of α-Aminomethylphosphonic Acids. Mannich-Type Reactions with Orthophosphorous Acid". The Journal of Organic Chemistry 31 (5): 1603. doi:10.1021/jo01343a067.

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