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41700

4,N,N-Trimethylaniline

purum, ≥98.0% (GC)

Synonym(s):

4-Dimethylaminotoluene, N,N-Dimethyl-p-toluidine

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About This Item

Linear Formula:
CH3C6H4N(CH3)2
CAS Number:
99-97-8
Molecular Weight:
135.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329756139
EC Number:
202-805-4
Beilstein/REAXYS Number:
774409
MDL number:
MFCD00008316
Assay:
≥98.0% (GC)
Form:
liquid

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vapor density

>1 (vs air)

Quality Level

100

grade

purum

assay

≥98.0% (GC)

form

liquid

expl. lim.

7 %

refractive index

n20/D 1.546 (lit.), n20/D 1.547

bp

211 °C (lit.), 90-92 °C/10 mmHg (lit.)

density

0.937 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CN(C)c1ccc(C)cc1

InChI

1S/C9H13N/c1-8-4-6-9(7-5-8)10(2)3/h4-7H,1-3H3

InChI key

GYVGXEWAOAAJEU-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
41690D189006592609
4,N,N-Trimethylaniline purum, ≥98.0% (GC)

Sigma-Aldrich

41700

4,N,N-Trimethylaniline

4,N,N-Trimethylaniline ≥98.5% (GC)

Sigma-Aldrich

41690

4,N,N-Trimethylaniline

4,N,N-Trimethylaniline 99%

Sigma-Aldrich

D189006

4,N,N-Trimethylaniline

4-Ethynyl-N,N-dimethylaniline 97%

Sigma-Aldrich

592609

4-Ethynyl-N,N-dimethylaniline

assay

≥98.0% (GC)

assay

≥98.5% (GC)

assay

99%

assay

97%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

-

refractive index

n20/D 1.546 (lit.), n20/D 1.547

refractive index

n20/D 1.546 (lit.), n20/D 1.547

refractive index

n20/D 1.546 (lit.)

refractive index

-

bp

90-92 °C/10 mmHg (lit.), 211 °C (lit.)

bp

211 °C (lit.), 90-92 °C/10 mmHg (lit.)

bp

211 °C (lit.), 90-92 °C/10 mmHg (lit.)

bp

-

form

liquid

form

liquid

form

liquid

form

solid

density

0.937 g/mL at 25 °C (lit.)

density

0.936 g/mL at 20 °C, 0.937 g/mL at 25 °C (lit.)

density

0.937 g/mL at 25 °C (lit.)

density

-

General description

4,N,N-Trimethylaniline is a N-methyl-N-alkylaniline. Its reaction with vinyl ether catalyzed by CuCl2 has been reported to afford tetrahydroquinolines.[1] Its radical cation undergoes reaction with the anthracene radical anion and generation of electrogenerated chemiluminescence (ECL) has been observed.[2]

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

ppe

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

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Carc. 1B - Repr. 2 - Skin Sens. 1 - STOT RE 2

target_organs

Respiratory Tract,Blood

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM0762
BCCN3301
BCCK5924
BCCK9749
BCCH2130

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Zoe M Wright et al.
Advanced healthcare materials, 10(2), e2001189-e2001189 (2020-12-17)
Graphene oxide and functionalized graphenic materials (FGMs) have promise as platforms for imparting programmable bioactivity to poly(methyl methacrylate) (PMMA)-based bone cement. To date, however, graphenic fillers have only been feasible in PMMA cements at extremely low loadings, limiting the bioactive
Xianghua Yang et al.
Molecules (Basel, Switzerland), 11(12), 978-987 (2007-11-17)
Tetrahydroquinoline skeletons can be formed by a CuCl2-catalyzed one-pot reaction of N-methyl-N-alkylanilines and vinyl ethers in the presence of t-butyl-hydroperoxide.
Jacob B Ketter et al.
Journal of the American Chemical Society, 126(32), 10183-10189 (2004-08-12)
Electrogenerated chemiluminescence (ECL) arising from the reaction of radical ions has previously be shown to arise from a variety of states including excited singlets, triplets, excimers, and exciplexes. In this work we describe two systems that form emissive states in
Y Nomura et al.
Journal of materials science. Materials in medicine, 17(1), 29-32 (2006-01-04)
The polymerization initiators for resins cured using visible light usually consist of a photosensitizer, primarily camphorquinone (CQ), and a reducing agent, which is often a tertiary amine (DMPT, DMAEMA), while the initiator used for self-curing resins consists of benzoyl peroxide
Yi-Ching Li et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 84(1), 58-63 (2007-04-25)
9-Fluorenone (9F), the aromatic photosensitizer, is widely used as an initiator in visible-light (VL) cured resin systems. There is growing concern that 9F may produce genetic damage by inducing mutation. In this study, 9F in the presence or absence of
View All Related Papers

Global Trade Item Number

SKUGTIN
41700-1L04061832090016
41700-250ML04061832090047

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