I0631
Imidodiphosphate sodium salt
≥97%
Synonym(s):
Tetrasodium imidodiphosphate
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About This Item
Linear Formula:
HNO6P2Na4
CAS Number:
Molecular Weight:
264.92
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
Certificates of Analysis (COA)
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Soong Yu Kuo et al.
Journal of plant physiology, 162(2), 129-138 (2005-03-23)
Endoplasmic reticulum (ER)-enriched vesicles from etiolated hypocotyls of mung bean seedlings (Vigna radiata) were successfully isolated using Ficoll gradient and two-phase (polyethylene glycol-dextran) partition. The ER-enriched vesicles contained inorganic pyrophosphate (PPi) hydrolysis and its associated proton translocating activities. Antiserum prepared
Peter Höök et al.
The Journal of biological chemistry, 280(38), 33045-33054 (2005-07-21)
The dynein motor domain consists of a ring of six AAA domains with a protruding microtubule-binding stalk and a C-terminal domain of unknown function. To understand how conformational information is communicated within this complex structure, we produced a series of
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
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
N F Zakirova et al.
Bioorganicheskaia khimiia, 31(1), 96-102 (2005-03-25)
The preparation conditions for dichlorophosphinylphosphorimidic trichloride were optimized. It was used in the synthesis of esters of imidodiphosphoric acid. The interaction of the trichloride with amines resulted in the corresponding amidodiphosphates rather than in the expected amides of imidodiphosphoric acid.
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