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Merck

773212

Sigma-Aldrich

N,N- 二乙基丙烯酰胺

contains <200 ppm MEHQ as inhibitor, 99%

别名:

N,N-二乙基-2-丙烯酰胺, DEAA, DEAAm, DEAM, 丙烯酸二乙酰胺

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About This Item

经验公式(希尔记法):
C7H13NO
CAS号:
分子量:
127.18
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

品質等級

化驗

99%

形狀

liquid

包含

<200 ppm MEHQ as inhibitor

折射率

n20/D 1.468

密度

0.924 at 25 °C

儲存溫度

2-8°C

SMILES 字串

CCN(CC)C(=O)C=C

InChI

1S/C7H13NO/c1-4-7(9)8(5-2)6-3/h4H,1,5-6H2,2-3H3

InChI 密鑰

OVHHHVAVHBHXAK-UHFFFAOYSA-N

應用

丙烯酰胺单体用于制备药物输送聚合物;热响应性聚合物;和具有经专门调整的LCST的溶液。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

192.0 °F

閃點(°C)

88.89 °C


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Nuran Işıklan et al.
Carbohydrate polymers, 218, 112-125 (2019-06-22)
Pectin based micro/nanocarriers display promising properties for biomedical applications. In this study, thermo/pH-responsive chitosan coated pectin-graft-poly(N,N-diethyl acrylamide) (Pec-g-PDEAAm/CS) microcarriers containing 5-Fluorouracil (5-FU) as a model drug were developed. The structure, thermal stability and surface morphology of 5-FU-loaded microcarriers were investigated
Wei Wei et al.
Colloids and surfaces. B, Biointerfaces, 136, 1182-1192 (2015-11-23)
Salecan is a water-soluble microbial polysaccharide produced by Agrobacterium sp. ZX09, a salt-tolerant strain isolated from a soil sample in our laboratory. Previous work inspired us salecan is a good candidate to fabricate hydrogels. Poly(N,N-diethylacrylamide) is one type of thermo
Xuemei Wu et al.
Sensors (Basel, Switzerland), 18(10) (2018-10-10)
In this work, binary hydrogel films based on carboxylated multi-walled carbon nanotubes/poly(N,N-diethylacrylamide) (c-MWCNTs/PDEA) were successfully polymerized and assembled on a glassy carbon (GC) electrode surface. The electroactive drug probes matrine and sophoridine in solution showed reversible thermal-, salt-, methanol- and
Z Ding et al.
Nature, 411(6833), 59-62 (2001-05-03)
Many medical and biotechnological processes rely on controlling and manipulating the molecular-recognition capabilities of proteins. This can be achieved using small molecules capable of competing for protein binding or by changing environmental parameters that affect protein structure and hence binding.
Okano, T.;
J. Controlled Release, 11, 255-265 (1990)

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