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About This Item
Linear Formula:
C6H5N(CH3)2
CAS Number:
Molecular Weight:
121.18
Beilstein:
507140
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
SAJ first grade
Assay
≥99.0%
form
liquid
availability
available only in Japan
refractive index
n20/D 1.557 (lit.)
pH
7.4 (20 °C, 1.2 g/L)
bp
193-194 °C (lit.)
mp
1.5-2.5 °C (lit.)
density
0.956 g/mL at 25 °C (lit.)
SMILES string
CN(C)c1ccccc1
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point(F)
143.6 °F
Flash Point(C)
62 °C
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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
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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