DISODIUM CHROMOTROPATE DIHYDRATE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H6O8S2.2Na.2H2O
Molecular Weight	400.29
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of DISODIUM CHROMOTROPATE DIHYDRATE

Structure Search

SMILES

O.O.[Na+].[Na+].OC1=CC(=CC2=CC(=CC(O)=C12)S([O-])(=O)=O)S([O-])(=O)=O

InChI

InChIKey=QUEAKWJKJBFNEG-UHFFFAOYSA-L

InChI=1S/C10H8O8S2.2Na.2H2O/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8;;;;/h1-4,11-12H,(H,13,14,15)(H,16,17,18);;;2*1H2/q;2*+1;;/p-2

HIDE SMILES / InChI

Molecular Formula	C10H8O8S2
Molecular Weight	320.296
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	Na
Molecular Weight	22.9898
Charge	1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	HO
Molecular Weight	17.0073
Charge	-1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses.	1971 Jul	4365198
Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids.	1990 Aug	2261142
Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities.	1992 Dec 25	1282569
Continuous flow system for the determination of trace boron in iron and steel utilizing in-line preconcentration/separation by Sephadex column coupled with fluorimetric detection.	2001 Aug 30	18968383
Resonance Rayleigh-scattering method for the determination of proteins with some monoazo dyes of chromotropic acid.	2001 Feb	11990533
Anion exchanger as a reaction/separation medium-absorptiometric determination of trace amounts of boron in waters by on-line complexation with chromotropic acid presorbed on the anion-exchange column.	2002 Dec	12537369
Preconcentration of lead with Amberlite XAD-2 and Amberlite XAD-7 based chelating resins for its determination by flame atomic absorption spectrometry.	2002 Mar 11	18968550
Chromotropic acid, a fluorogenic chelating agent for aluminium(III).	2004 Jan	14663545
Development of a solid surface fluorescence-based sensing system for aluminium monitoring in drinking water.	2005 Mar 15	18969932
Chromotropic acid-functionalized polyurethane foam: A new sorbent for on-line preconcentration and determination of cobalt and nickel in lettuce samples.	2006 Jun	16833076
Stepwise complexometric determination of aluminium, titanium and iron concentrations in silica sand and allied materials.	2007 Oct 19	17949493
Spectrophotometric determination of sildenafil citrate in pure form and in pharmaceutical formulation using some chromotropic acid azo dyes.	2010 Apr	20129817
Novel naphthalene-based inhibitors of Trypanosoma brucei RNA editing ligase 1.	2010 Aug 24	20808768
Ultraviolet spectrophotometric method for determination of gelatin crosslinking in the presence of amino groups.	2010 Jan	21331199
Fruit and soil quality of organic and conventional strawberry agroecosystems.	2010 Sep 1	20824185

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 06:08:02 GMT 2023` Edited by `admin` on `Sat Dec 16 06:08:02 GMT 2023`
Record UNII	Z441AY339V
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

DISODIUM CHROMOTROPATE DIHYDRATE

Common Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 4,5-DIHYDROXY-, SODIUM SALT, HYDRATE (1:2:2)

Common Name

English

CHROMOTROPIC ACID DISODIUM SALT DIHYDRATE [MI]

Common Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 4,5-DIHYDROXY-, DISODIUM SALT, DIHYDRATE

Common Name

English

CHROMOTROPIC ACID DISODIUM SALT DIHYDRATE

Common Name

English

Code System Code Type Description

FDA UNII

Z441AY339V