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Phenosafranin

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Phenosafranin Basic information

Product Name:
Phenosafranin
Synonyms:
  • 3,7-DIAMINO-5-PHENYLPHENAZINIUM CHLORIDE
  • CI 50200
  • CI NO 50200
  • 3,7-diamino-5-phenyl-phenaziniuchloride
  • nsc9855
  • Phenazinium,3,7-diamino-5-phenyl-,chloride
  • phenosafranine,chloride
  • 2,8-DiaMino-10-phenyl-phenaziniuM Chloride
CAS:
81-93-6
MF:
C18H15ClN4
MW:
322.8
EINECS:
201-387-0
Product Categories:
  • Amines
  • Aromatics
  • Mutagenesis Research Chemicals
Mol File:
81-93-6.mol
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Phenosafranin Chemical Properties

Melting point:
300 °C
Boiling point:
478.49°C (rough estimate)
Density 
1.1738 (rough estimate)
refractive index 
1.6110 (estimate)
storage temp. 
room temp
Colour Index 
50200
Merck 
13,7333
BRN 
3642082
CAS DataBase Reference
81-93-6
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
SG1630000

MSDS

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Phenosafranin Usage And Synthesis

Chemical Properties

green crystalline powder

Uses

Phenosafranin is a bacterial stain used in microscopy, biological stain, and nuclear staining.

Definition

ChEBI: Phenosafranine is an organic chloride salt having 3,7-diamino-5-phenylphenazin-5-ium as the counterion. It is commonly used for staining Gram negative bacteria red in smears to contrast with the blue Gram positive organisms. It has a role as a fluorochrome, a histological dye and a photosensitizing agent. It contains a 3,7-diamino-5-phenylphenazin-5-ium.

Biochem/physiol Actions

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

Staining Procedures

Phenosafranin is used to distinguish living from dead cells. A 0.1 % aqueous solution, it is taken up by dead or abnormal cells immediately, while living cells remain unstained for at least 30 min.

Purification Methods

Crystallise the chloride from dilute HCl. It has UV with at 530nm in H2O. The picrate decomposes on heating and has a solubility of 0.0048% in H2O at 18o. [Beilstein 23 H 395, Beilstein 25 H 394, 25 I 654, 25 II 338, 25 III/IV 3050.]

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