661376
2,3-Diaminophenazine
90%
Synonym(s):
2,3-Phenazinediamine
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About This Item
Empirical Formula (Hill Notation):
C12H10N4
CAS Number:
Molecular Weight:
210.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-512-0
MDL number:
Assay:
90%
Form:
solid
InChI key
VZPGINJWPPHRLS-UHFFFAOYSA-N
InChI
1S/C12H10N4/c13-7-5-11-12(6-8(7)14)16-10-4-2-1-3-9(10)15-11/h1-6H,13-14H2
SMILES string
Nc1cc2nc3ccccc3nc2cc1N
assay
90%
form
solid
mp
>300 °C
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S Sylvestre et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 401-412 (2012-06-23)
Vibrational analysis of the planar electron-rich heterocyclic 2,3-diaminophenazine (DAP) molecule was carried out using FT-IR and FT-Raman spectroscopic techniques. The equilibrium geometry, harmonic vibrational wavenumbers, various bonding features have been computed using density functional method. The calculated molecular geometry parameters
T Soulis et al.
Diabetologia, 42(4), 472-479 (1999-05-07)
Previous studies in our laboratory have shown that the vascular changes in diabetes include hypertrophy of the mesenteric vasculature and that this process can be attenuated by the inhibition of advanced glycation with aminoguanidine. Since aminoguanidine can also act as
Georgiana Roman-Gusetu et al.
Journal of chromatography. A, 1216(47), 8270-8276 (2009-09-22)
Microencapsulation is used here as a new technique to immobilize enzymes in a microreactor coupled off-line to capillary electrophoresis (CE), allowing the determination of enzymatic reaction products. The redox enzyme laccase was encapsulated using the method of interfacial cross-linking of
A Cebulska-Wasilewska et al.
Mutation research, 446(1), 57-65 (1999-12-29)
This paper presents studies on the genotoxicity of two aminophenazines: 2,3-diaminophenazine (DAP) and 2-amino-3-hydroxyphenazine (AHP). The genotoxic activities of these compounds were evaluated with human lymphocytes using the alkaline single cell gel electrophoresis (SCGE) assay and two cytogenetic assays (chromosome
T Watanabe et al.
Mutation research, 245(1), 15-22 (1990-09-01)
The mutagenicity of o- and m-phenylenediamine (PD) was remarkedly enhanced by oxidation; their major mutagenic oxidation products were 2,3- and 2,7-diaminophenazine, respectively. In order to evaluate the modulation effect of p-PD on the oxidation of m- or o-PD, p-PD and
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