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Merck
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T22500

Sigma-Aldrich

N,N,N′,N′-Tetramethylethylenediamine

ReagentPlus®, 99%

Synonyme(s) :

1,2-Bis(dimethylamino)ethane, TEMED, TMEDA

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About This Item

Formule linéaire :
(CH3)2NCH2CH2N(CH3)2
Numéro CAS:
Poids moléculaire :
116.20
Numéro Beilstein :
1732991
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Niveau de qualité

Gamme de produits

ReagentPlus®

Pureté

99%

Limite d'explosivité

9.08 %

Indice de réfraction

n20/D 1.4179 (lit.)

Point d'ébullition

120-122 °C (lit.)

Pf

−55 °C (lit.)

Densité

0.775 g/mL at 20 °C (lit.)

Chaîne SMILES 

CN(C)CCN(C)C

InChI

1S/C6H16N2/c1-7(2)5-6-8(3)4/h5-6H2,1-4H3

Clé InChI

KWYHDKDOAIKMQN-UHFFFAOYSA-N

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Catégories apparentées

Application

N,N,N′,N′-Tetramethylethylenediamine may be used as an initiator along with ammonium persulfate for polymerization reactions.

Informations légales

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

FlameSkull and crossbonesCorrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

61.7 °F - closed cup

Point d'éclair (°C)

16.5 °C - closed cup

Équipement de protection individuelle

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


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Cationic nanogels of N-isopropylacrylamide (NIPAM), including NIPAM-based cationic fluorescent nanogel thermometers, were synthesized with a cationic radical initiator previously developed in our laboratory. These cationic nanogels were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential measurements
Structure and Dynamics of Poly (N-isopropylacrylamide)? Clay Nanocomposite Gels.
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The methodological advancements in CIEF in tubes and microchips during the period between 2002 and early 2008 are reviewed as a continuation of previous review by the same author (Electrophoresis 2002, 23, 3847-3857). After a brief introduction, the following topics
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Inorganic chemistry, 49(4), 2008-2015 (2010-01-26)
Reactions of (en*)Pd(NO(3))(2) (en* = N,N,N',N'-tetramethylethylenediamine)with a series of organic bridging ligands of pyrazine, 1,2-bis(4-pyridyl)ethylene, 1,2-bis(4-pyridyl)acetylene, and 1,4-bis(4-pyridyl)benzene are carried out to investigate factors controlling the supramolecular structures and the equilibrium between the molecular triangles and the squares in solutions.
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Journal of combinatorial chemistry, 11(3), 338-340 (2009-03-06)
A practical and promising protocol was developed for S-arylations of various thiols with different substituted aryl halides. The reactions were readily facilitated to afford desired thioethers under mild conditions in good to excellent yields. The versatility, air-stability, operational simplicity of

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