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Merck
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文件

177342

Sigma-Aldrich

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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About This Item

线性分子式:
(CH3)2C6H3N(CH3)2
CAS号:
4913-13-7
分子量:
149.23
Beilstein:
1933736
EC號碼:
225-539-0
MDL號碼:
MFCD00008307
分類程式碼代碼:
12352100
PubChem物質ID:
24850628
NACRES:
NA.22

化驗

97%

形狀

liquid

折射率

n20/D 1.544 (lit.)

bp

226-228 °C (lit.)

密度

0.913 g/mL at 25 °C (lit.)

SMILES 字串

CN(C)c1cc(C)cc(C)c1

InChI

1S/C10H15N/c1-8-5-9(2)7-10(6-8)11(3)4/h5-7H,1-4H3

InChI 密鑰

NBFRQCOZERNGEX-UHFFFAOYSA-N

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相关类别

應用

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.

象形圖

Health hazardExclamation mark
GHS08,GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

195.8 °F - closed cup

閃點（°C）

91 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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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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