U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula 2Na.HO3P.5H2O
Molecular Weight 216.0358
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM PHOSPHITE PENTAHYDRATE

SMILES

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

InChI

InChIKey=VCNBZJAEINSDQB-UHFFFAOYSA-L
InChI=1S/2Na.H3O3P.5H2O/c;;1-4(2)3;;;;;/h;;4H,(H2,1,2,3);5*1H2/q2*+1;;;;;;/p-2

HIDE SMILES / InChI
The phosphonic acid functional group, which is characterized by a phosphorus atom bonded to three oxygen atoms (two hydroxy groups and one P=O double bond) and one carbon atom, is employed for many applications due to its structural analogy with the phosphate moiety or to its coordination or supramolecular properties. Phosphonic acids were used for their bioactive properties (drug, pro-drug), for bone targeting, for the design of supramolecular or hybrid materials, for the functionalization of surfaces, for analytical purposes, for medical imaging or as phosphoantigen. Potassium salt of phosphonic acid can be a declared or undeclared component of (foliar) fertilizers or plant strengtheners that were authorized in organic farming.

Approval Year

PubMed

PubMed

TitleDatePubMed
Isolation and biochemical characterization of hypophosphite/2-oxoglutarate dioxygenase. A novel phosphorus-oxidizing enzyme from Psuedomonas stutzeri WM88.
2002-10-11
Purification and characterization of a novel phosphorus-oxidizing enzyme from Pseudomonas stutzeri WM88.
2001-05-18
Patents
Name Type Language
SODIUM PHOSPHITE PENTAHYDRATE
MI  
Systematic Name English
ETIDRONATE DISODIUM RELATED COMPOUND A
USP-RS  
Preferred Name English
DISODIUM PHOSPHITE PENTAHYDRATE
Systematic Name English
ETIDRONATE DISODIUM RELATED COMPOUND A [USP-RS]
Common Name English
SODIUM PHOSPHITE PENTAHYDRATE [MI]
Common Name English
ETIDRONATE DISODIUM RELATED COMPOUND A [USP IMPURITY]
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1268513
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY
CAS
13517-23-2
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY
FDA UNII
UM5UZ43YVE
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY
MERCK INDEX
m10063
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID001337296
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY
SMS_ID
300000029175
Created by admin on Mon Mar 31 20:44:47 GMT 2025 , Edited by admin on Mon Mar 31 20:44:47 GMT 2025
PRIMARY