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Merck
CN

I7375

Iodonitrotetrazolium violet-formazan

crystalline

Synonym(s):

1-(4-Iodophenyl)-5-(4-nitrophenyl)-3-phenylformazan, INT-Formazan, Iodonitrotetrazolium formazan

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About This Item

Empirical Formula (Hill Notation):
C19H14IN5O2
CAS Number:
Molecular Weight:
471.25
UNSPSC Code:
12352204
NACRES:
NA.83
PubChem Substance ID:
EC Number:
231-950-6
Beilstein/REAXYS Number:
1829738
MDL number:
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Product Name

Iodonitrotetrazolium violet-formazan, crystalline

InChI key

FVFWUNAWQMROIF-CDNKMLFNSA-N

InChI

1S/C19H14IN5O2/c20-15-6-8-16(9-7-15)21-23-19(14-4-2-1-3-5-14)24-22-17-10-12-18(13-11-17)25(26)27/h1-13,22H/b23-21?,24-19-

SMILES string

[O-][N+](=O)c1ccc(NN=C(N=Nc2ccc(I)cc2)c3ccccc3)cc1

form

crystalline

color

brown

solubility

DMF: 50 mg/mL

storage temp.

2-8°C

Quality Level

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Application


  • Starvation-survival processes of a marine Vibrio.: This research explores the use of Iodonitrotetrazolium Violet-Formazan for studying the starvation-survival mechanisms in marine Vibrio, highlighting its application as a metabolic activity indicator under nutrient-deprived conditions, which is crucial for understanding bacterial survival strategies in natural aquatic environments (Amy et al., 1983).

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

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, Faceshields, Gloves


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Akashdeep Singh Oberoi et al.
Ecotoxicology and environmental safety, 135, 337-346 (2016-10-23)
In the present study, an attempt was made to understand the variation in the toxicity during the biodegradation of aromatic hydrocarbons in single and multi-substrate system. The bacterial bioassay based on the inhibition of dehydrogenase enzyme activity of two different
Marybeth A Pysz et al.
Experimental cell research, 315(8), 1415-1428 (2009-02-24)
Alterations in PKC isozyme expression and aberrant induction of cyclin D1 are early events in intestinal tumorigenesis. Previous studies have identified cyclin D1 as a major target in the antiproliferative effects of PKCalpha in non-transformed intestinal cells; however, a link

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