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Merck
CN

177342

3,5,N,N-Tetramethylaniline

97%

Synonym(s):

5-(Dimethylamino)-m-xylene, N,N-Dimethyl-sym.-xylidene

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About This Item

Linear Formula:
(CH3)2C6H3N(CH3)2
CAS Number:
4913-13-7
Molecular Weight:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24850628
EC Number:
225-539-0
Beilstein/REAXYS Number:
1933736
MDL number:
MFCD00008307
Assay:
97%
Form:
liquid

Key Documents

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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

Quality Level

200

bp

226-228 °C (lit.)

density

0.931 g/mL at 25 °C (lit.)

functional group

amine

Related Categories

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.

pictograms

Health hazardExclamation mark
GHS08,GHS07

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

Storage Class

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8303
BCCL3100
STBJ9483
STBH1575
STBF6497V

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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
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
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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