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I0631

Sigma-Aldrich

Imidodiphosphate sodium salt

≥97%

Synonym(s):

Tetrasodium imidodiphosphate

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About This Item

Linear Formula:
HNO6P2Na4
CAS Number:
26039-10-1
Molecular Weight:
264.92
EC Number:
247-423-9
MDL number:
MFCD26142276
UNSPSC Code:
12352100
PubChem Substance ID:
57654288
NACRES:
NA.22

Assay

≥97%

storage temp.

2-8°C

SMILES string

O=P([O-])([O-])NP([O-])([O-])=O.[Na+].[Na+].[Na+].[Na+]

InChI

1S/H5NO6P2.4Na/c2-8(3,4)1-9(5,6)7;;;;/h(H5,1,2,3,4,5,6,7);;;;/q;4*+1/p-4

InChI key

KDZOOFFPQVQSQG-UHFFFAOYSA-J

Related Categories

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

I0631-5G:
I0631-250MG:
I0631-BULK:
I0631-1G:
I0631-VAR:

Certificates of Analysis (COA)

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Anna M Rydzik et al.
Bioorganic & medicinal chemistry, 20(5), 1699-1710 (2012-02-10)
We describe synthesis and properties of eight dinucleotide mRNA 5' cap analogs containing imidodiphosphate moiety within 5',5'-tri- or tetraphosphate bridge (NH-analogs). The compounds were obtained by coupling an appropriate nucleoside 5'-imidodiphosphate with nucleotide P-imidazolide mediated by divalent metal chloride in
George D Markham et al.
Biochemistry, 43(12), 3415-3425 (2004-03-24)
S-Adenosylmethionine synthetase (ATP: L-methionine S-adenosyltransferase) catalyzes a two-step reaction in which tripolyphosphate (PPPi) is a tightly bound intermediate. Diimidotriphosphate (O(3)P-NH-PO(2)-NH-PO(3); PNPNP), a non-hydrolyzable analogue of PPPi, is the most potent known inhibitor of AdoMet synthetase with a K(i) of 2
A B Zyryanov et al.
Biochemistry. Biokhimiia, 70(8), 908-912 (2005-10-11)
Imidodiphosphate (the pyrophosphate analog containing a nitrogen atom in the bridge position instead of oxygen) is a potent inhibitor of family II pyrophosphatases from Streptococcus mutans and Streptococcus gordonii (inhibition constant Ki approximately 10 microM), which is slowly hydrolyzed by
Highly efficient green and blue-green phosphorescent OLEDs based on iridium complexes with the tetraphenylimidodiphosphinate ligand.
Yu-Cheng Zhu et al.
Advanced materials (Deerfield Beach, Fla.), 23(35), 4041-4046 (2011-07-30)
T Rozovskaya et al.
FEBS letters, 247(2), 289-292 (1989-04-24)
It is demonstrated here that rat liver DNA polymerase beta catalyzes the pyrophosphorolysis reaction with pyrophosphate (PPi) and its analogues. The substrate specificity of the PPi-binding site of several DNA polymerases was investigated. It was discovered that the ability of
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