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V800269

Sigma-Aldrich

N,N-Dimethylaniline

LR, ≥99%

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About This Item

Fórmula linear:
C6H5N(CH3)2
Número CAS:
121-69-7
Peso molecular:
121.18
Beilstein:
507140
Número CE:
204-493-5
Número MDL:
MFCD00008304
Código UNSPSC:
12352100
ID de substância PubChem:
329829267

grau

LR

linha de produto

Vetec™

Ensaio

≥99%

forma

liquid

índice de refração

n20/D 1.557 (lit.)

pH

7.4 (20 °C, 1.2 g/L)

pb

193-194 °C (lit.)

pf

1.5-2.5 °C (lit.)

densidade

0.956 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CN(C)c1ccccc1

InChI

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

chave InChI

JLTDJTHDQAWBAV-UHFFFAOYSA-N

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Informações legais

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

167.0 °F - closed cup

Ponto de fulgor (°C)

75 °C - closed cup

Certificados de análise (COA)

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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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