336408

Sigma-Aldrich

trans-4-[4-(Dimethylamino)styryl]-1-methylpyridinium iodide

Dye content 98 %

Sinónimos:
(E )-4-[4-(Dimethylamino)styryl]-1-methylpyridinium iodide, Pyridinium, 4-[2-[4-(dimethylamino)phenyl]ethenyl]-1-methyl-, iodide,
Empirical Formula (Hill Notation):
C16H19IN2
Número de CAS:
Peso molecular:
366.24
MDL number:
PubChem Substance ID:

composition

Dye content, 98%

Quality Level

mp

254-256 °C (lit.)

λmax

475 nm

SMILES string

[I-].[H]\C(=C(\[H])c1cc[n+](C)cc1)c2ccc(cc2)N(C)C

InChI

1S/C16H19N2.HI/c1-17(2)16-8-6-14(7-9-16)4-5-15-10-12-18(3)13-11-15;/h4-13H,1-3H3;1H/q+1;/p-1

InChI key

UJNFDSOJKNOBIA-UHFFFAOYSA-M

Categorías relacionadas

General description

trans-4-[4-(dimethylamino)-styryl]-1-methylpyridinium iodide (DASPI) is a hemicyanine dye.
trans-4-[4-(Dimethylamino)styryl]-1-methylpyridinium iodide (DASP) is a hemicyanine dye that can be used as a fluorescence probe. Its fluorescent property can be tuned by adjusting the pH of the solution. It can be photoexcited for internal twisting that forms intermolecular charge transfer state.

Application

DASP can be used to characterize the fluorescence of zeolite crystals which can further be used in the development of photofunctional materials.

Packaging

1 g in glass bottle

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Excited-State Photophysics and Dynamics of a Hemicyanine Dye in AOT Reverse Micelles
Kim J and Lee M
The Journal of Physical Chemistry A, 103 (18), 3378?3382-3378?3382 null
Large fluorescence enhancement of a hemicyanine by supramolecular interaction with cucurbit [6] uril and its application as resettable logic gates
Li Z, et al.
Dyes and Pigments, 93(1-3), 1401-1407 (2012)
Effects of external pressure and solvent polarity on inclusion complexations of phenothiazine dyes and trans-4-[4-(dimethylamino) styryl]-1-methylpyridinium with water-soluble p-sulfonatocalix [8] arene in alcohol-water mixtures
Sueishi Y and Asano K
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 63(1-2), 37-42 (2009)
Groove binding of a styrylcyanine dye to the DNA double helix: the salt effect
Kumar CV, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 74(2-3), 231-238 (1993)
Excited-state photophysics and dynamics of a hemicyanine dye in AOT reverse micelles
Kim J and Lee M
The Journal of Physical Chemistry A, 103(18), 3378-3382 (1999)

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