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39255

Sigma-Aldrich

4-Dimethylamino-4′-nitrostilbene

≥99.8% (T)

Sinónimos:

N,N-Dimethyl-4′-nitro-4-stilbenamine, DANS

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About This Item

Fórmula lineal:
(CH3)2NC6H4CH=CHC6H4NO2
Número de CAS:
2844-15-7
Peso molecular:
268.31
Beilstein/REAXYS Number:
1379389
MDL number:
MFCD00041877
UNSPSC Code:
12352108
PubChem Substance ID:
57649889
NACRES:
NA.32

assay

≥99.8% (T)

form

solid

mp

256-259 °C (lit.)
256-259 °C

fluorescence

λex 500 nm; λem ~700 nm in methylene chloride

SMILES string

CN(C)c1ccc(\C=C\c2ccc(cc2)[N+]([O-])=O)cc1

InChI

1S/C16H16N2O2/c1-17(2)15-9-5-13(6-10-15)3-4-14-7-11-16(12-8-14)18(19)20/h3-12H,1-2H3/b4-3+

InChI key

NVLSIZITFJRWPY-ONEGZZNKSA-N

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Application

4-Dimethylamino-4′-nitrostilbene (DANS, DMANS) may be used as a proton/acid indicator and physical chemistry probe to study state energy and photoexcitation dynamics of molecules.

Other Notes

Standard for the correction of emission of fluorescence spectrometers

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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I D Petsalakis et al.
The journal of physical chemistry. A, 114(17), 5580-5587 (2010-04-14)
A theoretical investigation on the electronic structure of 4-dimethylamino-4'-nitrostilbene (DANS), 4-(dicyanomethylene)-2-methyl-6-p-(dimethylamino) styryl-4H-pyran (DCM), and their protonated forms is presented in an effort to rationalize recent experimental results on the tuning of the emitted color of organic light-emitting diodes through photochemically
Charles A Schmuttenmaer
Science progress, 85(Pt 2), 175-197 (2002-09-10)
The direct measurement of intramolecular electron transfer through detection of the electromagnetic (EM) waveform that is emitted during this process is reviewed. The waveform is detected in the time-domain via free-space electro-optic sampling and then related to the dynamics of
Takakazu Nakabayashi et al.
Journal of the American Chemical Society, 127(19), 7041-7052 (2005-05-12)
External electric field effects on state energy and photoexcitation dynamics have been examined for para-substituted and unsubstituted all-trans-diphenylpolyenes doped in a film, based on the steady-state and picosecond time-resolved measurements of the field effects on absorption and fluorescence. The substitution
Antonio Barbon et al.
Physical chemistry chemical physics : PCCP, 8(43), 5069-5078 (2006-11-09)
Two dyes (4-nitrostilbene, NST and 4-N,N-dimethylamino-4'-nitrostilbene, DANS) included in zeolites with nanometric channels and different Si : Al ratios have been photoexcited and their triplet state studied by time resolved EPR (TR-EPR). This is the first time that a TR-EPR
E. Lippert et al.
Z. Anal. Chem., 170, 1-1 (1959)
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