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462314

Sigma-Aldrich

Iminodi(methylphosphonic acid)

97%

Synonym(s):

Aminobis(methylenephosphonic acid), Bis(phosphonomethyl)amine, Iminobis(methylene)bis(phosphonic acid), Iminobis[methylenephosphonic acid], Iminodimethylenediphosphonic acid, Iminodimethylenephosphonic acid, P,P′-[Iminobis(methylene)]bis[phosphonic acid]

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About This Item

Linear Formula:
HN[CH2PO(OH)2]2
CAS Number:
Molecular Weight:
205.04
Beilstein/REAXYS Number:
1812882
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

mp

220 °C (dec.) (lit.)

solubility

water: soluble

SMILES string

OP(O)(=O)CNCP(O)(O)=O

InChI

1S/C2H9NO6P2/c4-10(5,6)1-3-2-11(7,8)9/h3H,1-2H2,(H2,4,5,6)(H2,7,8,9)

InChI key

ISQSUCKLLKRTBZ-UHFFFAOYSA-N

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General description

Iminodi(methylphosphonic acid) is an iminopolyphosphonic acid derivative. It is widely used as complex forming reagent for alkylphosphonic groups. Thermal analysis has confirmed the anhydrous state of iminodi(methylphosphonic acid).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Iminodi (methylphosphonic) acid.
Afonin, E. G.
Russ. J. Gen. Chem., 73(10), 1503-1505 (2003)
Scott A Lujan et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(30), 12282-12287 (2007-07-17)
Conjugative transfer of plasmid DNA via close cell-cell junctions is the main route by which antibiotic resistance genes spread between bacterial strains. Relaxases are essential for conjugative transfer and act by cleaving DNA strands and forming covalent phosphotyrosine linkages. Based

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