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MilliporeSigma

09341

Sigma-Aldrich

8-Aminopyrene-1,3,6-trisulfonic acid trisodium salt

suitable for fluorescence, BioReagent, ≥96.0% (HPCE)

Synonym(s):

1,3,6-Pyrenetrisulfonic acid, 8-amino trisodium salt, APTS, Trisodium 8-aminopyrene-1,3,6-trisulfonate

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About This Item

Empirical Formula (Hill Notation):
C16H8NNa3O9S3
CAS Number:
196504-57-1
Molecular Weight:
523.40
MDL number:
MFCD00674494
UNSPSC Code:
12352106
PubChem Substance ID:
329748761
NACRES:
NA.32

Key Documents

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product line

BioReagent

Quality Level

200

assay

≥96.0% (HPCE)

mp

≥250 °C (lit.)

solubility

DMF: soluble
DMSO: soluble
H2O: soluble

fluorescence

λex 420 nm; λem 500 nm in 0.1 M Tris pH 7.4 (quenching with Vitamin B1)
λex 488 nm; λem 520 nm(lit.)

suitability

suitable for fluorescence

SMILES string

[Na+].[Na+].[Na+].Nc1cc(c2ccc3c(cc(c4ccc1c2c34)S([O-])(=O)=O)S([O-])(=O)=O)S([O-])(=O)=O
[Na+].[Na+].[Na+].Nc1cc(c2ccc3c(cc(c4ccc1c2c34)S([O-])(=O)=O)S([O-])(=O)=O)S([O-])(=O)=O

InChI

1S/C16H11NO9S3.3Na/c17-11-5-12(27(18,19)20)8-3-4-10-14(29(24,25)26)6-13(28(21,22)23)9-2-1-7(11)15(8)16(9)10;;;/h1-6H,17H2,(H,18,19,20)(H,21,22,23)(H,24,25,26);;;/q;3*+1/p-3

InChI key

XSTNYACEWLNWPY-UHFFFAOYSA-K

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Application

APTS is a fluorescence reagent that has been demonstrated to have a high level of detection sensitivity for sugars The LOD for APTS-derivatized sugars has been shown to be 0.4 nM when using a 488 nm argon-ion laser. The multi-anionic nature of APTS makes it ideal for the studies of carbohydrate molecules and small hormone molecules by high resolution capillary electrophoresis.
Fluorescent label for glycoproteins and saccharides.
Fluorescent label for saccharides and glycoproteins.

Other Notes

Fluorescent probe for derivatising sugars

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ6915
BCBS0182V
BCBK9934V
BCBK5407V

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R.A. Evangelista et al.
Analytical Chemistry, 67, 2239-2239 (1995)
H Suzuki et al.
Analytical chemistry, 69(22), 4554-4559 (1998-01-07)
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), has been used for structure characterization of 1-aminopyrene-3,6,8-trisulfonate (APTS)-derivatized oligosaccharides previously separated by capillary electrophoresis (CE). The resolved components were first isolated by employing an automated high-resolution fraction collector. Using on-probe sample
Michael S Gilmore et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(23), 7273-7278 (2015-06-04)
Multidrug-resistant Enterococcus faecalis possess numerous mobile elements that encode virulence and antibiotic resistance traits as well as new metabolic pathways, often constituting over one-quarter of the genome. It was of interest to determine how this large accretion of mobile elements
Jie Chen et al.
PloS one, 10(6), e0127022-e0127022 (2015-06-16)
The aim of this study was to evaluate the diagnostic and differential diagnostic power of serum N-glycans for light chain multiple myeloma (LCMM). A total of 167 cases of subjects, including 42 LCMM, 42 IgG myeloma, 41 IgA myeloma, and
Shuoran Chen et al.
Advanced materials (Deerfield Beach, Fla.), 27(26), 3928-3933 (2015-05-27)
Nanoscale circuits are fabricated by assembling different conducting materials (e.g., metal nanoparticles, metal nano-wires, graphene, carbon nanotubes, and conducting polymers) on inkjet-printing patterned substrates. This non-litho-graphy strategy opens a new avenue for integrating conducting building blocks into nanoscale devices in
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