2,6-NAPHTHALENEDISULFONIC ACID

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H8O6S2
Molecular Weight	288.297
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 2,6-NAPHTHALENEDISULFONIC ACID

Structure Search

SMILES

OS(=O)(=O)C1=CC=C2C=C(C=CC2=C1)S(O)(=O)=O

InChI

InChIKey=FITZJYAVATZPMJ-UHFFFAOYSA-N

InChI=1S/C10H8O6S2/c11-17(12,13)9-3-1-7-5-10(18(14,15)16)4-2-8(7)6-9/h1-6H,(H,11,12,13)(H,14,15,16)

HIDE SMILES / InChI

Molecular Formula	C10H8O6S2
Molecular Weight	288.297
Charge	0
Count

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

Approval Year

PubMed

Title	Date	PubMed
Sensitized enantioselective laser-induced phosphorescence detection in chiral capillary electrophoresis.	2010-11-15	20964317
pH-operated nanopistons on the surfaces of mesoporous silica nanoparticles.	2010-09-22	20799689
Dissociation of dicarboxylate and disulfonate dianions.	2010-03-07	20210392
Analytical conditions and separation performance of capillary chromatography based on the tube radial distribution of aqueous-organic mixture carrier solvents under laminar-flow conditions.	2010	20631432
Capillary chromatography based on tube radial distribution of aqueous-organic mixture carrier solvents: introduction of double tubes having different inner diameters to the system.	2010	20410577
Capillary chromatography based on the tube radial distribution of aqueous-organic mixture carrier solvents: effects of the inner-wall characteristics of the fused-silica tube on separation performance.	2009-11	19907097
Capillary chromatography based on tube radial distribution of aqueous-organic mixture carrier solvents.	2009-10-15	19635369
Micro-flow separation system using an open capillary tube that works under laminar flow conditions.	2009-02	19212043
Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges.	2008-10-21	18827940
Cooperativity and selectivity in chemomechanical polyethylenimine gels.	2007-10-09	17824717
Organic anion recognition of naphthalenesulfonates by steroid-modified beta-cyclodextrins: enhanced molecular binding ability and molecular selectivity.	2006-08-04	16872183
Mutational analysis of the metabolism of 2,6-naphthalenedisulfonate by Pigmentiphaga sp. NDS-2.	2003	16233443
Diaquabis(ethylenediamine)copper(II) bis[tris(ethylenediamine)nickel(II)] tris(naphthalene-2,6-disulfonate) tetrahydrate.	2001-10	11600774
Protonation effects on the inclusion complexation of 6-deoxy-6-diethylamino-beta-cyclodextrin with 2-anthracenesulfonate, 2-naphthalenesulfonate, 2,6-naphthalenedisulfonate, and 2,7-naphthalenedisulfonate in aqueous solutions.	2001-01	11209851

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:01:50 GMT 2025` Edited by `admin` on `Mon Mar 31 19:01:50 GMT 2025`
Record UNII	BOR133U3TN
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

2,6-NAPHTHALENEDISULFONIC ACID

Systematic Name

English

EBERT-MERZ .BETA.-ACID

Preferred Name

English

2,6-NAPHTHALENEDISULFONIC ACID [MI]

Common Name

English

NSC-37041

Code

English

NAPHTHALENE-2,6-DISULPHONIC ACID

Systematic Name

English

Code System Code Type Description

FDA UNII

BOR133U3TN