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P2508

Sigma-Aldrich

Proflavine hemisulfate salt hydrate

powder

Synonym(s):

3,6-Diaminoacridine hemisulfate salt

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About This Item

Empirical Formula (Hill Notation):
C13H11N3 · 0.5 H2SO4 · xH2O
CAS Number:
1811-28-5
Molecular Weight:
258.29 (anhydrous basis)
Beilstein:
3921806
EC Number:
217-320-3
MDL number:
MFCD00149650
UNSPSC Code:
12171500
PubChem Substance ID:
24898329
NACRES:
NA.47

form

powder

solubility

H2O: 10 mg/mL

fluorescence

λex 444 nm; λem 508 nm (0.01M HCl)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[H]O[H].OS(O)(=O)=O.Nc1ccc2cc3ccc(N)cc3nc2c1.Nc4ccc5cc6ccc(N)cc6nc5c4

InChI

1S/2C13H11N3.H2O4S.H2O/c2*14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;1-5(2,3)4;/h2*1-7H,14-15H2;(H2,1,2,3,4);1H2

InChI key

DTRLDKDFCPUGCA-UHFFFAOYSA-N

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General description

Proflavine is a small, amphipathic, acridine-derived fluorescent dye.Proflavine hemisulfate is used as a rapid stain for cytological studies of biological specimens. It stains cytoplasmic structures and nuclei. Proflavine has the capability to intercalate double stranded DNA.

Application

Proflavine hemisulfate salt hydrate has been used to stain cells of the 1483 cell line. It has also been used as a calibrating dye in fluorescence resonance energy transfer (FRET) analysis.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A Orth et al.
Science advances, 5(4), eaav1555-eaav1555 (2019-04-30)
Optical fiber bundle microendoscopes are widely used for visualizing hard-to-reach areas of the human body. These ultrathin devices often forgo tunable focusing optics because of size constraints and are therefore limited to two-dimensional (2D) imaging modalities. Ideally, microendoscopes would record
Robust approaches to quantitative ratiometric FRET imaging of CFP/YFP fluorophores under confocal microscopy
M. R. Tadross
Journal of Microscopy (2009)
Improving spatial resolution of a fiber bundle optical biopsy system
Matthew Kyrish
Proceedings of SPIE (2010)
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology
Sandra P. Prieto
PLoS ONE, 10(5) (2015)
Emma V Ainsworth et al.
Chembiochem : a European journal of chemical biology, 17(24), 2324-2333 (2016-09-30)
The transfer of photoenergized electrons from extracellular photosensitizers across a bacterial cell envelope to drive intracellular chemical transformations represents an attractive way to harness nature's catalytic machinery for solar-assisted chemical synthesis. In Shewanella oneidensis MR-1 (MR-1), trans-outer-membrane electron transfer is

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