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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O3S
Molecular Weight 208.234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-NAPHTHALENESULFONIC ACID

SMILES

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

InChI

InChIKey=PSZYNBSKGUBXEH-UHFFFAOYSA-N
InChI=1S/C10H8O3S/c11-14(12,13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,11,12,13)

HIDE SMILES / InChI
Molecular Formula C10H8O3S
Molecular Weight 208.234
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Determination of naphthalenesulfonic acid isomers by large-volume on-line derivatization and gas chromatography-mass spectrometry.
2001 Aug 17
Characterization of a partially folded intermediate of stem bromelain at low pH.
2002 Jan
Final report on the amended safety assessment of sodium polynaphthalenesulfonate and sodium naphthalenesulfonate.
2003
The unique aromatic catabolic genes in sphingomonads degrading polycyclic aromatic hydrocarbons (PAHs).
2003 Feb
Leads for development of new naphthalenesulfonate derivatives with enhanced antiangiogenic activity: crystal structure of acidic fibroblast growth factor in complex with 5-amino-2-naphthalene sulfonate.
2003 Jun 13
Trifluoroethanol-induced "molten globule" state in stem bromelain.
2003 May 15
Analysis of naphthalenesulfonate compounds by cyclodextrin-mediated capillary electrophoresis with sample stacking.
2003 May 9
Separation and migration behavior of positional and structural naphthalenesulfonate isomers by cyclodextrin-mediated capillary electrophoresis.
2004 Apr 9
Inactivation of NADP+-dependent isocitrate dehydrogenase by lipid peroxidation products.
2004 Mar
Ozonation of naphthalenesulphonic acid in the aqueous phase in the presence of basic activated carbons.
2004 Oct 12
Low versus high molecular weight poly(ethylene glycol)-induced states of stem bromelain at low pH: stabilization of molten globule and unfolded states.
2006 Apr 5
A chromatographic estimate of the degree of surface heterogeneity of reversed-phase liquid chromatography packing materials. II-Endcapped monomeric C18-bonded stationary phase.
2006 Jan 20
Identification and functional analysis of the genes for naphthalenesulfonate catabolism by Sphingomonas xenophaga BN6.
2006 Jul
Osmolyte trimethylamine N-oxide converts recombinant alpha-helical prion protein to its soluble beta-structured form at high temperature.
2006 Sep 29
Native-like tertiary structure in the Mucor miehei lipase molten globule state obtained at low pH.
2007 Mar
A review of current intravaginal drug delivery approaches employed for the prophylaxis of HIV/AIDS and prevention of sexually transmitted infections.
2008
Membrane bioreactors for municipal wastewater treatment - a viable option to reduce the amount of polar pollutants discharged into surface waters?
2008 Aug
Detection of conformational changes in immunoglobulin G using isothermal titration calorimetry with low-molecular-weight probes.
2008 Sep 15
Benzyl-tributyl-ammonium 6,7-dihydroxy-naphthalene-2-sulfonate.
2009 Jan 17
Benzyl-tributyl-ammonium 4,6-dihydroxy-naphthalene-2-sulfonate.
2009 Jan 17
Discovery and mechanistic study of a class of protein arginine methylation inhibitors.
2010 Aug 26
How informed is consent in vulnerable populations? Experience using a continuous consent process during the MDP301 vaginal microbicide trial in Mwanza, Tanzania.
2010 Jun 13
Interaction of imidacloprid with hemoglobin by fluorescence and circular dichroism.
2010 May
Targeting tumor angiogenesis with TSP-1-based compounds: rational design of antiangiogenic mimetics of endogenous inhibitors.
2010 Nov
Physiology and biochemistry of reduction of azo compounds by Shewanella strains relevant to electron transport chain.
2010 Oct
Effective and specific inhibition of the CD40-CD154 costimulatory interaction by a naphthalenesulphonic acid derivative.
2010 Oct
Biofoams and natural protein surfactants.
2010 Oct
Patents

Patents

03989661
7
03993663
2
04939064
2
05093229
2
JP1075589A
2
JP1079296A
2
JP2000302603A
2
JP2000327968A
2
JP2002088365A
2
JP2003082378A
2
JP2003192621A
8
JP2003226874A
2
JP2004148173A
2
JP2004318049A
9
JP2005336170A
2
JP2007142070A
2
JP2008024926A
2
JP2009173929A
2
JP2009517308A
2
JP2011195984A
2
JP3120091B2
9
JP4359817B2
2
JP4682207B2
2
JP4763128B2
3
JPH00680966A
2
JPH01113499A
2
JPH01113500A
2
JPH01138274A
3
JPH01252697A
2
JPH0195198A
2
JPH03157479A
2
JPH03209359A
2
JPH03209360A
2
JPH03210335A
2
JPH04189872A
2
JPH04211046A
2
JPH04314889A
2
JPH04314896A
2
JPH04370101A
2
JPH055002A
2
JPH06172764A
2
JPH08109389A
2
JPH08188459A
2
JPH0840835A
2
JPH09241640A
2
JPH101620A
2
JPH1036306A
2
JPH11335996A
2
JPH1172969A
2
JPS05599907A
2
JPS05686996A
2
JPS05867781A
2
JPS5470345A
2
JPS55142092A
2
JPS5599907A
2
JPS56147864A
2
JPS562361A
2
JPS562362A
2
JPS5686996A
2
JPS5784552A
2
JPS58194962A
2
JPS5861115A
2
JPS5867781A
2
JPS59215356A
2
JPS60130672A
5
JPS60255824A
2
JPS6071693A
2
JPS6155157A
2
JPS62129385A
2
JPS62156159A
2
JPS62169894A
2
JPS62253667A
2
JPS63135480A
2
JPS6466295A
2
JPS6475589A
2
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:54:56 GMT 2023
Edited
by admin
on Fri Dec 15 18:54:56 GMT 2023
Record UNII
0SJH61WM2J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-NAPHTHALENESULFONIC ACID
MI  
Systematic Name English
1-NAPHTHALENESULFONIC ACID [MI]
Common Name English
HT-907
Code English
.ALPHA.-NAPHTHALENESULFONIC ACID
Systematic Name English
1-SULFONAPHTHALENE
Systematic Name English
Code System Code Type Description
CAS
85-47-2
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
FDA UNII
0SJH61WM2J
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
WIKIPEDIA
Naphthalene-1-sulfonic acid
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
PUBCHEM
6812
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-610-1
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
MERCK INDEX
m7731
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID7048033
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
CHEBI
30895
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY
RXCUI
1442718
Created by admin on Fri Dec 15 18:54:56 GMT 2023 , Edited by admin on Fri Dec 15 18:54:56 GMT 2023
PRIMARY RxNorm
Related Record Type Details
Structure of POTASSIUM NAPHTHALENE-1-SULFONATE
SALT/SOLVATE -> PARENT
Structure of LITHIUM NAPHTHALENESULPHONATE
SALT/SOLVATE -> PARENT
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