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About This Item
Linear Formula:
HN[CH2PO(OH)2]2
CAS Number:
Molecular Weight:
205.04
Beilstein:
1812882
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
220 °C (dec.) (lit.)
solubility
water: soluble
functional group
amine
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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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