Skip to Content
Merck
CN

462314

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]

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
HN[CH2PO(OH)2]2
CAS Number:
Molecular Weight:
205.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1812882
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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)

SMILES string

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

InChI key

ISQSUCKLLKRTBZ-UHFFFAOYSA-N

assay

97%

mp

220 °C (dec.) (lit.)

solubility

water: soluble

functional group

amine

Quality Level

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service