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Key Documents

39255

Sigma-Aldrich

4-Dimethylamino-4′-nitrostilbene

≥99.8% (T)

Sinonimo/i:

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

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About This Item

Formula condensata:
(CH3)2NC6H4CH=CHC6H4NO2
Numero CAS:
Peso molecolare:
268.31
Beilstein:
1379389
Numero MDL:
Codice UNSPSC:
12352108
ID PubChem:
NACRES:
NA.32

Saggio

≥99.8% (T)

Forma fisica

solid

Punto di fusione

256-259 °C (lit.)
256-259 °C

Fluorescenza

λex 500 nm; λem ~700 nm in methylene chloride

Stringa SMILE

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+
NVLSIZITFJRWPY-ONEGZZNKSA-N

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Applicazioni

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.

Altre note

Standard for the correction of emission of fluorescence spectrometers

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


Certificati d'analisi (COA)

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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
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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
E. Lippert et al.
Z. Anal. Chem., 170, 1-1 (1959)
Antonios M Douvas et al.
Inorganic chemistry, 48(11), 4896-4907 (2009-05-02)
The capability of ammonium 18-molybdodiphosphate, (NH(4))(6)P(2)Mo(18)O(62) (Mo(18)(6-)), and ammonium 18-tungstodiphosphate, (NH(4))(6)P(2)W(18)O(62) (W(18)(6-)), to photochemically generate acid within films of a polymer with hydroxylic functional groups (namely, within poly(2-hydroxyethyl methacrylate) (PHEMA) films) is demonstrated. Upon UV irradiation, both 2:18 polyoxometalates (POMs)
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

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