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714720

Sigma-Aldrich

4-(Dimethylamino)pyridine solution

0.5 M in ethyl acetate

Sinonimo/i:

DMAP solution

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About This Item

Formula empirica (notazione di Hill):
C7H10N2
Numero CAS:
1122-58-3
Peso molecolare:
122.17
Beilstein:
3539759
Numero MDL:
MFCD00006418
Codice UNSPSC:
12352005
ID PubChem:
329763308
NACRES:
NA.22

Forma fisica

liquid

Livello qualitativo

100

Concentrazione

0.5 M in ethyl acetate

Indice di rifrazione

n20/D 1.384

Densità

0.906 g/mL at 25 °C

Stringa SMILE

CN(C)c1ccncc1

InChI

1S/C7H10N2/c1-9(2)7-3-5-8-6-4-7/h3-6H,1-2H3
VHYFNPMBLIVWCW-UHFFFAOYSA-N

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Avvertenze

Danger

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 2 - STOT SE 3

Organi bersaglio

Central nervous system, Nervous system

Rischi supp

EUH066

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

26.6 °F - closed cup

Punto d’infiammabilità (°C)

-3.0 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
MKCJ7962
MKCJ2959
MKCH8475
MKBX2657V

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A M van Wijk et al.
Analytical and bioanalytical chemistry, 400(5), 1375-1385 (2011-03-30)
A generic LC-MS/MS method was developed for the analysis of potentially genotoxic alkyl halides. A broad selection of alkyl halides were derivatized using 4-dimethylaminopyridine in acetonitrile. The reaction conditions for derivatization, i.e., solvent, reaction time, temperature and concentration of alkyl
Chenghu Yan et al.
Biomacromolecules, 10(8), 2013-2018 (2009-09-03)
An effective method for grafting L-lactide (LA) from unmodified cellulose by ring-opening polymerization (ROP) in homogeneous mild conditions is presented. By using 4-dimethylaminopyridine (DMAP) as an organic catalyst, cellulose-graft-poly(L-lactide) (cellulose-g-PLLA) copolymers with a molar substitution (MS(PLLA)) of PLLA in a
Hangxiang Wang et al.
Journal of the American Chemical Society, 133(31), 12220-12228 (2011-07-19)
Catalysts hold promise as tools for chemical protein modification. However, the application of catalysts or catalyst-mediated reactions to proteins has only recently begun to be addressed, mainly in in vitro systems. By radically improving the affinity-guided DMAP (4-dimethylaminopyridine) (AGD) catalysts
Min Suk Shim et al.
Journal of controlled release : official journal of the Controlled Release Society, 133(3), 206-213 (2008-11-11)
To maximize therapeutic effects, targeted delivery of nucleic acids (e.g., DNA and RNA) in their appropriate intracellular targets is highly desirable. In this study, primary amines of a model polymeric nonviral carrier, polyethylenimine (PEI), at two molecular weights (0.8 and
Zheng Wang et al.
Analytical chemistry, 84(11), 4915-4920 (2012-04-28)
The development of highly sensitive and selective detection techniques for the discrimination of relevant toxic benzenethiols and biologically active aliphatic thiols is of considerable importance in the fields of chemical, biological, and environmental sciences. In this article, we describe a
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