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Details

Stereochemistry ACHIRAL
Molecular Formula C16H10O12S4
Molecular Weight 522.503
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3,6,8-PYRENETETRASULFONIC ACID

SMILES

OS(=O)(=O)C1=CC(=C2C=CC3=C(C=C(C4=C3C2=C1C=C4)S(O)(=O)=O)S(O)(=O)=O)S(O)(=O)=O

InChI

InChIKey=CZLSHVQVNDDHDQ-UHFFFAOYSA-N
InChI=1S/C16H10O12S4/c17-29(18,19)11-5-13(31(23,24)25)9-3-4-10-14(32(26,27)28)6-12(30(20,21)22)8-2-1-7(11)15(9)16(8)10/h1-6H,(H,17,18,19)(H,20,21,22)(H,23,24,25)(H,26,27,28)

HIDE SMILES / InChI

Molecular Formula C16H10O12S4
Molecular Weight 522.503
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Ultra-large single-layer graphene obtained from solution chemical reduction and its electrical properties.
2010-03-07
An improved strategy for the crystallization of Leishmania mexicana pyruvate kinase.
2010-03-01
Biophysical and functional characterization of an ion channel peptide confined in a sol-gel matrix.
2009-05-28
Structure analysis of hydrotalcite intercalated with pyrenetetrasulfonate; experiments and molecular modelling.
2008-12
Probing the conformation of polyelectrolytes in mesoporous silica spheres.
2008-04-15
Slow release of molecules in self-assembling peptide nanofiber scaffold.
2006-09-28
Solvent free microwave synthesis and evaluation of antimicrobial activity of pyrimido[4,5-b]- and pyrazolo[3,4-b]quinolines.
2006-06-01
Two-dimensional fluorescence correlation spectroscopy II: spectral analysis of derivatives of anthracene and pyrene in micellar solutions.
2004-07
Domain-specific effector interactions within the central cavity of human adult hemoglobin in solution and in porous sol-gel matrices: evidence for long-range communication pathways.
2004-04-27
Preparation of a water-in-oil-in-water (W/O/W) type microcapsules by a single-droplet-drying method and change in encapsulation efficiency of a hydrophilic substance during storage.
2003-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:11:16 GMT 2025
Edited
by admin
on Mon Mar 31 20:11:16 GMT 2025
Record UNII
CEZ11T634X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3,6,8-PYRENETETRASULFONIC ACID
Systematic Name English
1,3,6,8-PYRENE TETRASULFONATE
Preferred Name English
PYRENE-1,3,6,8-TETRASULPHONIC ACID
Systematic Name English
Code System Code Type Description
MESH
C041343
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
EPA CompTox
DTXSID5044310
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
CAS
6528-53-6
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
PUBCHEM
81017
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
FDA UNII
CEZ11T634X
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
ECHA (EC/EINECS)
229-423-0
Created by admin on Mon Mar 31 20:11:16 GMT 2025 , Edited by admin on Mon Mar 31 20:11:16 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT