177342
3,5,N,N-四甲基苯胺
97%
别名:
5-(二甲氨基)间二甲苯, N,N-Dimethyl-sym.-xylidene
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关于此项目
线性分子式:
(CH3)2C6H3N(CH3)2
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-539-0
Beilstein/REAXYS Number:
1933736
MDL number:
产品名称
3,5,N,N-四甲基苯胺, 97%
InChI key
NBFRQCOZERNGEX-UHFFFAOYSA-N
InChI
1S/C10H15N/c1-8-5-9(2)7-10(6-8)11(3)4/h5-7H,1-4H3
SMILES string
CN(C)c1cc(C)cc(C)c1
assay
97%
form
liquid
refractive index
n20/D 1.544 (lit.)
bp
226-228 °C (lit.)
density
0.913 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
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Application
3,5,N,N-Tetramethylaniline was used in rapid quenching of 1,8-dihydroxyanthraquinone (DHAQ). It was also used as a catalyst in the polymeric synthesis of glycol methacrylate.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
195.8 °F - closed cup
flash_point_c
91 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Sorina M Ulmeanu et al.
Pharmaceutical research, 20(8), 1317-1322 (2003-09-02)
A new experimental set-up for studying partitioning of ionizable drugs at the interface between two immiscible electrolyte solutions (ITIES) by amperometry is presented. The method is quite general, as it can be applied to any charged drug molecule. The procedure
M Sekiguchi et al.
Brain research. Developmental brain research, 64(1-2), 189-195 (1991-12-17)
To analyze developmental abnormalities related to neural migration in the NZB/BINJ mouse, the pattern of cerebellar foliation and neural position were compared with that of a normal mouse (C57BL/6J). Three abnormalities of cerebellar foliation--(1) lobe isolated from other cerebellar lobes
Yang Pan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(1), 63-67 (2006-07-04)
The property of the lowest excited triplet states of 1,8-dihydroxyanthraquinone (DHAQ) was investigated by using time-resolved laser flash photolysis at 355nm in organic solvents, i.e. acetonitrile and cyclohexane. The transient absorption spectra of the excited triplet DHAQ were obtained in
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