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D189006

Sigma-Aldrich

4,N,N-Trimethylaniline

99%

Sinonimo/i:

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

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About This Item

Formula condensata:
CH3C6H4N(CH3)2
Numero CAS:
99-97-8
Peso molecolare:
135.21
Beilstein:
774409
Numero CE:
202-805-4
Numero MDL:
MFCD00008316
Codice UNSPSC:
12352100
ID PubChem:
24893566
NACRES:
NA.22

Densità del vapore

>1 (vs air)

Livello qualitativo

200

Saggio

99%

Stato

liquid

Limite di esplosione

7 %

Indice di rifrazione

n20/D 1.546 (lit.)

P. ebollizione

211 °C (lit.)
90-92 °C/10 mmHg (lit.)

Densità

0.937 g/mL at 25 °C (lit.)

Stringa SMILE

CN(C)c1ccc(C)cc1

InChI

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

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Applicazioni

4,N,N-Trimethylaniline is a tertiary amine that can undergo iron-catalyzed oxidative C-C coupling with phenylacetylene and benzamide in the presence of tert-butylperoxide to form N,4-dimethyl-N-(3-phenylprop-2-ynyl)benzenamine and N-((methyl(p-tolyl)amino)methyl)benzamide, respectively.

Pittogrammi

Skull and crossbonesHealth hazard
GHS06,GHS08

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Reproductive organs

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

168.8 °F - closed cup

Punto d’infiammabilità (°C)

76 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
WXBD6295V
MKCQ2698
MKCQ1969
WXBD5675V
WXBD5358V

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Chemoselective C? H Bond Activation: Ligand and Solvent Free Iron-Catalyzed Oxidative C? C Cross-Coupling of Tertiary Amines with Terminal Alkynes. Reaction Scope and Mechanism.
Volla C M R, et al.
Organic Letters, 11(8), 1701-1704 (2009)
M Noda et al.
Journal of biomedical materials research. Part A, 83(1), 123-129 (2007-03-27)
Resin composites are widely used in dentistry, and are polymerized in situ using a blue-light activated, free-radical polymerization mechanism. Blue light (400-500nm) is used to activate camphoroquinone (CQ), which decomposes to form free radicals that are stabilized by dimethyl-p-toludine (DMPT).
Jennifer L Moreau et al.
Journal of biomedical materials research. Part A, 81(3), 594-602 (2006-12-21)
There is an increasing need to develop new biomaterials as tissue engineering scaffolds. Unfortunately, many of the materials that have been studied for these purposes are polyesters that hydrolytically degrade into acidic products, which may harm the surrounding tissue, and
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Mycoses, 45(8), 300-305 (2003-02-08)
The effects of four liquid components of denture acrylic resin on host cell activity and fungal adhesion were investigated in this study. The low concentration (1 micromol l(-1)) of the liquid components caused no change in the activities and morphologies
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
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Global Trade Item Number

SKUGTIN
D189006-100ML4061833561027
D189006-1L4061833561034
D189006-500ML4061836830694
D189006-5ML

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