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N3013

Nile Red

Powder

Synonym(s):

9-(diethylamino)-5H-benzo[a]phenoxazin-5-one, 9-(diethylamino)benzo[a]phenoxazin-5-one, Nile Blue A Oxazone

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100 MG

$140.00

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$765.00

$140.00


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About This Item

Empirical Formula (Hill Notation):
C20H18N2O2
CAS Number:
Molecular Weight:
318.37
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
230-966-0
MDL number:
Beilstein/REAXYS Number:
279110

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Product Name

Nile Red, Technical grade

InChI

1S/C20H18N2O2/c1-3-22(4-2)13-9-10-16-18(11-13)24-19-12-17(23)14-7-5-6-8-15(14)20(19)21-16/h5-12H,3-4H2,1-2H3

SMILES string

CCN(CC)c1ccc2N=C3C(Oc2c1)=CC(=O)c4ccccc34

InChI key

VOFUROIFQGPCGE-UHFFFAOYSA-N

grade

technical grade

form

powder

composition

Carbon: 70.0-77.3%

Nitrogen: 7.5-8.8%

technique(s)

titration: suitable

mp

203-205 °C (lit.)

solubility

methanol: 1 mg/mL

λmax

553 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

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1 of 4

This Item
N07661912372485
grade

technical grade

grade

certified by the Biological Stain Commission

grade

-

grade

for microscopy

technique(s)

titration: suitable

technique(s)

microbe id | staining: suitable

technique(s)

-

technique(s)

-

color

faint green to brown

color

dark green

color

-

color

-

solubility

methanol: 1 mg/mL

solubility

H2O: 1 mg/mL

solubility

-

solubility

-

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

-

application(s)

-

form

powder

form

powder

form

solid

form

crystals

Application

Nile red is widely employed in studies related to lipid metabolism, lipid droplet dynamics, lipid accumulation in cells or tissues, and lipid-based drug delivery systems. Its other applications include:
  • identification of microplastics in routine analysis of biological samples.[1]
  • detection of lysosomes and lysosome-related organelles, like gut granules in C. elegans intestinal cells.[2]
  • it exhibits strong fluorescence enhancement and is used for staining SDS (sodium dodecyl sulphate) gels.[3]

Biochem/physiol Actions

Nile Red is lipophilic in nature and exploits the hydrophobic properties of molecules such as lipids and plastics that fluoresce when excited with certain wavelengths, facilitating quantification and identification.[1]

General description

Nile Red is a lipophilic fluorescent benzophenoxazone dye that is metachromatic and solvatochromic.[1] It is an uncharged hydrophobic molecule with the ability to stain and visualize lipid droplets in cells and tissues.[4] It functions as a fluorescent probe for intracellular lipids and hydrophobic domains of proteins. This dye is fluorescent in all organic solvents. Its fluorescence colors range from golden yellow to deep red.[5]

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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D L Sackett et al.
Analytical biochemistry, 167(2), 228-234 (1987-12-01)
Nile red is an uncharged hydrophobic molecule whose fluorescence is strongly influenced by the polarity of its environment. It interacts with many, but not all, native proteins, including beta-lactoglobulin, kappa-casein, and albumin, with a wide range of spectral changes for
Autophagy gene disruption reveals a non-vacuolar cell death pathway in Dictyostelium.
Kosta A
The Journal of Biological Chemistry, 279, 48404-48404 (2004)
Protein gel staining methods: an introduction and overview
Thomas H Steinberg
Methods in Enzymology, 541-563 (2009)
Hanna Fares et al.
Methods in cell biology, 107, 239-263 (2012-01-10)
This chapter describes methods for studying membrane traffic and organelle biogenesis in Caenorhabditis elegans. These processes have traditionally been studied with yeast or mammalian cells, but C. elegans is emerging as an attractive alternative model system for cell biologists. C.
Luca Nalbone et al.
Marine pollution bulletin, 172, 112888-112888 (2021-08-29)
Nile Red is a lipophilic, metachromatic and solvatochromic dye used as an alternative or complementary method to aid identification of microplastics in routine analysis of biological samples. It was rarely used in biota since organic residues after the digestion step

Questions

  1. How should n3013 be dissolved and diluted for lipid staining?

    1 answer
    1. There has not been any conduct suitability testing for Nile Red. Please see the following for an article that may offer information; J. Histochem. Cytochem. 35:619-621 reference.
      To perform the staining, a stock solution of Nile red was prepared by dissolving 10 mg of Nile red in 10 ml of acetone, which was then stored in the refrigerator protected from light. The sections were fixed in 1% glutaraldehyde in PBS for 5 minutes and washed in PBS three times for 2 minutes each. The staining solution was then prepared by diluting 100 ul of the stock solution in 1 ml of PBS. The sections were covered with this solution for 20 minutes at room temperature, then briefly washed in PBS and mounted in 75% glycerol in PBS. Other sections were incubated with solutions containing 50, 10, and 1 ug and 100 ng of Nile red per ml. The sections were examined with a filter set for fluorescein fluorescence (450-500 nm band pass excitation filter, a 510 nm center wavelength chromatic beam splitter, and a 528 nm long-pass barrier filter) and were photographed.

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