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714720

Sigma-Aldrich

4-（二甲氨基）吡啶 溶液

0.5 M in ethyl acetate

别名:

DMAP 溶液

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About This Item

经验公式（希尔记法）:
C7H10N2
CAS号:
1122-58-3
分子量:
122.17
Beilstein:
3539759
MDL號碼:
MFCD00006418
分類程式碼代碼:
12352005
PubChem物質ID:
329763308
NACRES:
NA.22

形狀

liquid

濃度

0.5 M in ethyl acetate

折射率

n20/D 1.384

密度

0.906 g/mL at 25 °C

SMILES 字串

CN(C)c1ccncc1

InChI

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

InChI 密鑰

VHYFNPMBLIVWCW-UHFFFAOYSA-N

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訊號詞

Danger

危險分類

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

標靶器官

Central nervous system, Nervous system

安全危害

EUH066

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

26.6 °F - closed cup

閃點（°C）

-3.0 °C - closed cup

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCJ7962
MKCJ2959
MKCH8475
MKBX2657V

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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
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
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
Capture and visualization of hydrogen sulfide by a fluorescent probe.
Chunrong Liu et al.
Angewandte Chemie (International ed. in English), 50(44), 10327-10329 (2011-09-08)
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