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Merck
CN

41525

N,N-Dimethyl-6-propionyl-2-naphthylamine

BioReagent, suitable for fluorescence, ≥98.0% (HPLC)

Synonym(s):

2-(Dimethylamino)-6-propionylnaphthalene, 6-Propionyl-2-(dimethylamino)naphthalene, Prodan

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About This Item

Empirical Formula (Hill Notation):
C15H17NO
CAS Number:
70504-01-7
Molecular Weight:
227.30
UNSPSC Code:
12352116
NACRES:
NA.32
PubChem Substance ID:
57650063
MDL number:
MFCD00056615
Beilstein/REAXYS Number:
2723587

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InChI

1S/C15H17NO/c1-4-15(17)13-6-5-12-10-14(16(2)3)8-7-11(12)9-13/h5-10H,4H2,1-3H3

SMILES string

CCC(=O)c1ccc2cc(ccc2c1)N(C)C

InChI key

MPPQGYCZBNURDG-UHFFFAOYSA-N

product line

BioReagent

assay

≥98.0% (HPLC)

form

solid

Quality Level

100

solubility

DMF: soluble, acetone: soluble, acetonitrile: soluble, methanol: soluble

fluorescence

λex 361 nm; λem 498 nm in methanol

suitability

suitable for fluorescence

Related Categories

Application

N,N-Dimethyl-6-propionyl-2-naphthylamine (Prodan), a membrane surface probe, may be used as a fluorescence probe in non-cell based in vitro assay for the determination of drug-phospholipid complex formation and to study membrane surface properties.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Fluorescence of spectrin-bound Prodan

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCP1667
BCCL7745
BCCH9139
BCCH9138
BCCF1912

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Liping Zhou et al.
Analytical chemistry, 83(18), 6980-6987 (2011-07-28)
This paper describes for the first time, a high-throughput fluorescence noncell based assay to screen for the drug-phospholipid interaction, which correlates to phospholipidosis. Anionic amphiphilic phospholipids can form complexes in aqueous solution, and its critical micelle concentration (CMC) can be
A Chakrabarti
Biochemical and biophysical research communications, 226(2), 495-497 (1996-09-13)
A large blue-shift (delta lambda max = 87 nm) in the fluorescence emission maximum and 2-fold enhancement in the emission intensity of PRODAN in the presence of 1.5 microM dimeric spectrin from the same aqueous buffer was observed. Binding of
Praveen Gadad et al.
Water research, 41(19), 4488-4496 (2007-07-17)
Noncovalent interactions between the fluorescent probe 6-propionyl-2-dimethylaminonaphthalene (PRODAN) and dissolved Norman Landfill leachate fulvic acid, Suwannee River fulvic acid, Suwannee River humic acid, and Leonardite humic acid were examined as a function of pH, fulvic and humic acid (FA and
Kazuki Tainaka et al.
Journal of the American Chemical Society, 129(15), 4776-4784 (2007-03-24)
A solvatochromic fluorophore, PRODAN, has been used as a microenvironment-sensitive reporter. Based on the chemistry of PRODAN, we designed and synthesized four novel fluorescent nucleosides, PDNX (X = U, C, A, and G), to which a PRODAN fluorophore was attached
Paul Abbyad et al.
The journal of physical chemistry. B, 111(28), 8269-8276 (2007-06-27)
Proteins respond to electrostatic perturbations through complex reorganizations of their charged and polar groups, as well as those of the surrounding media. These solvation responses occur both in the protein interior and on its surface, though the exact mechanisms of
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