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199648

Sigma-Aldrich

Phenosafranin

Dye content 80 %

Sinonimo/i:

3,7-Diamino-5-phenylphenazinium chloride

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About This Item

Formula empirica (notazione di Hill):
C18H15ClN4
Numero CAS:
Peso molecolare:
322.79
Colour Index:
50200
Beilstein:
3642082
Numero CE:
Numero MDL:
Codice UNSPSC:
12171500
ID PubChem:
NACRES:
NA.47

Forma fisica

powder

Composizione

Dye content, 80%

tecniche

titration: suitable

Punto di fusione

>300 °C (lit.)

λmax

519 nm

applicazioni

diagnostic assay manufacturing
hematology
histology

Temperatura di conservazione

room temp

Stringa SMILE

[Cl-].Nc1ccc2nc3ccc(N)cc3[n+](-c4ccccc4)c2c1

InChI

1S/C18H14N4.ClH/c19-12-6-8-15-17(10-12)22(14-4-2-1-3-5-14)18-11-13(20)7-9-16(18)21-15;/h1-11H,(H3,19,20);1H
SOUHUMACVWVDME-UHFFFAOYSA-N

Applicazioni

Phenosafranin has been used for nuclear staining.

Azioni biochim/fisiol

Phenosafranin (PSF) is a red dye released from cells with intact plasma membrane. PSF at lower concentration is used to stain mitochondria supravitally.

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Vascular Streak Dieback of cacao in Southeast Asia and Melanesia: in planta detection of the pathogen and a new taxonomy
Samuels GJ
Fungal Biology, 116, 11-23 (2012)
Paramita Das et al.
The journal of physical chemistry. B, 111(38), 11169-11176 (2007-09-06)
A steady-state and time-resolved photophysical study of a cationic phenazinium dye, phenosafranin (PSF), has been investigated in well-characterized biomimetic micellar nanocavities formed by anionic surfactants of varying chain lengths, namely, sodium decyl sulfate (S(10)S), sodium dodecyl sulfate (S(12)S), and sodium
Paramita Das et al.
Journal of colloid and interface science, 320(1), 9-14 (2008-01-15)
We introduce a simple and efficient strategy to enhance the efficiency of a quenching-based fluorosensor for metal ions by several orders of magnitude by using commercially available anionic surfactants varying hydrophobic chain length. Anionic surfactants with a proper choice of
P E Hartman et al.
Photochemistry and photobiology, 51(1), 59-66 (1990-01-01)
Singlet molecular oxygen was generated by illumination of phenosafranin in phosphate buffer at pH 7.5. Relative efficiencies of various imidazole compounds to form endoperoxides were assayed by following at 25 degrees C the rate of light- and imidazole-dependent bleaching of
Farhana S Saleh et al.
Bioelectrochemistry (Amsterdam, Netherlands), 80(2), 121-127 (2010-07-30)
The electrochemical regeneration of NADH/NAD(+) redox couple has been studied using poly(phenosafranin) (PPS)-modified carbon electrodes to evaluate the formal potential and catalytic rate constant for the oxidation of NADH. The PPS-modified electrodes were prepared by electropolymerization of phenosafranin onto different

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