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Key Documents

82658

Sigma-Aldrich

1,3,6,8-Pyrenetetrasulfonic acid tetrasodium salt hydrate

suitable for fluorescence, ≥98% (HPLC)

Synonym(s):

Tetrasodium 1,3,6,8-pyrenetetrasulfonate hydrate

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About This Item

Empirical Formula (Hill Notation):
C16H6Na4O12S4 · xH2O
Molecular Weight:
610.43 (anhydrous basis)
Beilstein/REAXYS Number:
3646090
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.32

Quality Level

assay

≥98% (HPLC)

form

crystals

impurities

≤15% water

suitability

suitable for fluorescence

SMILES string

O.[Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)c1cc(c2ccc3c(cc(c4ccc1c2c34)S([O-])(=O)=O)S([O-])(=O)=O)S([O-])(=O)=O

InChI

1S/C16H10O12S4.4Na.H2O/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);;;;;1H2/q;4*+1;/p-4

InChI key

LZDOYGMJVXUZGD-UHFFFAOYSA-J

Application

1,3,6,8-Pyrenetetrasulfonic acid tetrasodium salt hydrate has been used as a ligand or a crystallisation additive in facilitating protein−protein contacts through cation−π interactions.

Other Notes

Fluorescent probe

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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N. Kobayashi
Journal of the Chemical Society. Chemical Communications, 918-918 (1988)
Protein camouflage: supramolecular anion recognition by ubiquitin
MalloN M, et al.
Chembiochem, 17(8), 774-783 (2016)
Bruno Mattei et al.
Chemistry and physics of lipids, 202, 28-37 (2016-12-04)
Detergents are widely used to solubilize and separate biomembrane components. It is therefore relevant to study and understand the mechanistic details underlying detergent-lipid interactions using biomimetic systems. Here, we have investigated in detail the process of membrane permeabilization and the
E. Koller
Appl. Fluoresc. Technol., 1, 13-13 (1989)

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