41690
4,N,N-三甲基苯胺
≥98.5% (GC)
别名:
4-二甲氨基甲苯, N,N-二甲基-对甲苯胺
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关于此项目
线性分子式:
CH3C6H4N(CH3)2
化学文摘社编号:
分子量:
135.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-805-4
Beilstein/REAXYS Number:
774409
MDL number:
Assay:
≥98.5% (GC)
Form:
liquid
vapor density
>1 (vs air)
Quality Level
assay
≥98.5% (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
0.936 g/mL at 20 °C, 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
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. Its radical cation undergoes reaction with the anthracene radical anion and generation of electrogenerated chemiluminescence (ECL) has been observed.
Application
- Charge-transfer complexes for redox polymerization: 4,N,N-Trimethylaniline used for on-demand amine/peroxide redox polymerization. This research offers a new perspective on the use of 4,N,N-Trimethylaniline in creating controlled polymer structures, which is crucial for various industrial and pharmaceutical applications (Garra et al., 2018).
Disclaimer
储存中可能变成黄绿色
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Danger
存储类别
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
target_organs
Respiratory Tract,Blood
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
法规信息
新产品
此项目有
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
Sachiko Kaihara et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 68(1), 67-73 (2007-09-25)
While many synthetic, hydrolytically degradable hydrogels have been developed for biomedical applications, there are only a few examples whose polymer backbone does not form acidic products upon degradation. In order to address this concern, we proposed to develop a hydrogel
Chiemi Hirabayashi et al.
Dental materials journal, 21(4), 314-321 (2003-03-01)
Polymerization characteristics of poly (methyl methacrylate)(PMMA)/(methyl methacrylate) (MMA) resin initiated by tributylborane (TBB) were compared with those by benzoyl peroxide (BPO)/N,N-dimethyl-p-toluidine and camphorquinone (CQ)/N,N-dimethylaminoethyl methacrylate from the aspects of temporal changes of residual MMA and molecular weight up to 4
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 41690-500ML | 04061836826857 |
| 41690-100ML | 04061832089911 |