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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

Nome Commerciale

Vetec

Saggio

≥99%

Stato

liquid

dilution

(for analytical testing)

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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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
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
Jiyun Park et al.
Inorganic chemistry, 50(22), 11612-11622 (2011-10-21)
Oxidative dimerization of N,N-dimethylaniline (DMA) occurs with a nonheme iron(IV)-oxo complex, [Fe(IV)(O)(N4Py)](2+) (N4Py = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine), to yield the corresponding dimer, tetramethylbenzidine (TMB), in acetonitrile. The rate of the oxidative dimerization of DMA by [Fe(IV)(O)(N4Py)](2+) is markedly enhanced by the presence
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
Haider Raza et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 139(4), 289-293 (2005-02-03)
We previously reported the occurrence of multiple forms of drug metabolizing enzymes in camel tissues. In this study, we demonstrated for the first time, flavin-containing monooxygenase (FMO)-dependent metabolism of two model substrates methimazole (MEM) and N,N'-dimethylaniline (DMA) by camel liver

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