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经验公式(希尔记法):
C18H15ClN4
化学文摘社编号:
分子量:
322.79
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
Colour Index Number:
50200
EC Number:
201-387-0
MDL number:
Beilstein/REAXYS Number:
3642082
InChI key
SOUHUMACVWVDME-UHFFFAOYSA-N
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
SMILES string
[Cl-].Nc1ccc2nc3ccc(N)cc3[n+](-c4ccccc4)c2c1
form
powder
composition
Dye content, 80%
technique(s)
titration: suitable
mp
>300 °C (lit.)
λmax
519 nm
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
Application
酚藏花红已被用于核染色。
Biochem/physiol Actions
酚红素(PSF)是一种由具有完整质膜的细胞所释放的红色染料。较低浓度的PSF可用来对线粒体进行离体活体染色。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
G. A. Swan
Phenazines (2009)
Deboleena Sarkar et al.
The journal of physical chemistry. A, 112(40), 9684-9691 (2008-09-13)
Absorption, fluorescence, and fluorescence excitation spectral studies of two planar, cationic phenazinium dyes, namely, phenosafranin (PSF) and safranin-T (ST), have been performed in protic and aprotic polar solvents. The studies reveal the formation of both J- and H-aggregates in concentrated
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
Ishita Saha et al.
The journal of physical chemistry. B, 114(46), 15278-15287 (2010-10-29)
The sequence selectivity of the DNA binding of the phenazinium dyes phenosafranin and safranin O have been investigated with four sequence-specific deoxyribopolynucleotides from spectroscopic and calorimetric studies. The alternating guanine-cytosine sequence selectivity of the dyes has been revealed from binding
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