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Documenti fondamentali

V800269

Sigma-Aldrich

N,N-Dimethylaniline

LR, ≥99%

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About This Item

Formula condensata:
C6H5N(CH3)2
Numero CAS:
Peso molecolare:
121.18
Beilstein:
507140
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
Grado:
LR
Saggio:
≥99%
P. ebollizione:
193-194 °C (lit.)

Grado

LR

Nome Commerciale

Vetec

Saggio

≥99%

Stato

liquid

Indice di rifrazione

n20/D 1.557 (lit.)

pH

7.4 (20 °C, 1.2 g/L)

P. ebollizione

193-194 °C (lit.)

Punto di fusione

1.5-2.5 °C (lit.)

Densità

0.956 g/mL at 25 °C (lit.)

Stringa SMILE

CN(C)c1ccccc1

InChI

1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3
JLTDJTHDQAWBAV-UHFFFAOYSA-N

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Note legali

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

167.0 °F - closed cup

Punto d’infiammabilità (°C)

75 °C - closed cup


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Cai-Rong Zhang et al.
Journal of molecular graphics & modelling, 38, 419-429 (2012-11-03)
The photon to current conversion efficiency of dye-sensitized solar cells (DSCs) can be significantly affected by dye sensitizers. The design of novel dye sensitizers with good performance in DSCs depend on the dye's information about electronic structures and optical properties.
Haijun Li et al.
Organic letters, 11(18), 4176-4179 (2009-08-18)
Methylene-bridged bis-1,3-dicarbonyl derivatives were synthesized efficiently by iron-catalyzed oxidative reactions of 1,3-dicarbonyl compounds and N,N-dimethylaniline. Bipyrazoles and substituted 1,4-dihydropyridine were obtained by the reactions of bis-1,3-dicarbonyl compounds with hydrazines and ammonium acetate, respectively.
Zhiwei Lin et al.
Journal of the American Chemical Society, 131(50), 18060-18062 (2009-11-26)
Ultrafast UV-vibrational spectroscopy was used to investigate how vibrational excitation of the bridge changes photoinduced electron transfer between donor (dimethylaniline) and acceptor (anthracene) moieties bridged by a guanosine-cytidine base pair (GC). The charge-separated (CS) state yield is found to be
Atanu Kumar Das et al.
The journal of physical chemistry. B, 115(16), 4680-4688 (2011-04-07)
Ultrafast photoinduced electron transfer (PET) from N,N-dimethylaniline (DMA) to coumarin dyes in a room-temperature ionic liquid (RTIL, [pmim][BF(4)]) and in a mixed micelle containing the RTIL and a triblock copolymer, (PEO)(20)-(PPO)(70)-(PEO)(20), (Pluronic P123) is studied using femtosecond upconversion. A Marcus-like
Anjan Chakraborty et al.
The Journal of chemical physics, 128(20), 204510-204510 (2008-06-03)
Photoinduced electron transfer between coumarin dyes and N,N-dimethylaniline has been investigated by using steady state and picosecond time resolved fluorescence spectroscopy in sodium dodecyl sulphate (SDS) micelles and PVP-polyvinyl pyrrolidone (SDS) polymer-surfactant aggregates. A slower rate of electron transfer is

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