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Merck
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文件

M6762

Sigma-Aldrich

1-甲基-2-吡咯烷酮

同義詞:

N-甲基-2-吡咯烷酮, N-甲基吡咯烷酮, NMP

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About This Item

經驗公式（希爾表示法）:
C5H9NO
CAS號碼:
872-50-4
分子量：:
99.13
Beilstein:
106420
EC號碼:
212-828-1
MDL號碼:
MFCD00003193
分類程式碼代碼:
12352005
PubChem物質ID:
329818036

蒸汽密度

3.4 (vs air)

蒸汽壓力

0.29 mmHg ( 20 °C)
0.99 mmHg ( 40 °C)

自燃溫度

518 °F

expl. lim.

9.5 %

折射率

n20/D 1.47 (lit.)

bp

202 °C (lit.)
81-82 °C/10 mmHg (lit.)

mp

−24 °C (lit.)

溶解度

ethanol: miscible 0.1 mL/mL, clear, colorless (10%, v/v)
H2O: miscible
acetone: miscible
benzene: miscible
chloroform: miscible
diethyl ether: miscible
ethyl acetate: miscible

密度

1.028 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CN1CCCC1=O

InChI

1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3

InChI 密鑰

SECXISVLQFMRJM-UHFFFAOYSA-N

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其他說明

This product has been replaced by M79603-Sigma-Aldrich | 1-Methyl-2-pyrrolidinone, ReagentPlus®, 99% | C5H9NO

法律資訊

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

象形圖

Health hazardExclamation mark
GHS08,GHS07

訊號詞

Danger

危險分類

Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類（WGK）

WGK 1

閃點（°F）

195.8 °F - Pensky-Martens closed cup

閃點（°C）

91 °C - Pensky-Martens closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

分析證明 (COA)

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B A Jönsson et al.
Journal of chromatography. B, Biomedical sciences and applications, 694(2), 351-357 (1997-07-04)
A method for simultaneous determination of 5-hydroxy-N-methylpyrrolidone and 2-hydroxy-N-methylsuccinimide in urine is described. These compounds are metabolites of N-methyl-2-pyrrolidone, a powerful and widely used organic solvent. 5-Hydroxy-N-methylpyrrolidone and 2-hydroxy-N-methylsuccinimide were purified from urine by adsorption to a C8 solid-phase extraction
Chun-Wa Chung et al.
Journal of medicinal chemistry, 55(2), 576-586 (2011-12-06)
Bromodomain-containing proteins are key epigenetic regulators of gene transcription and readers of the histone code. However, the therapeutic benefits of modulating this target class are largely unexplored due to the lack of suitable chemical probes. This article describes the generation
David S Hewings et al.
Journal of medicinal chemistry, 54(19), 6761-6770 (2011-08-20)
Histone-lysine acetylation is a vital chromatin post-translational modification involved in the epigenetic regulation of gene transcription. Bromodomains bind acetylated lysines, acting as readers of the histone-acetylation code. Competitive inhibitors of this interaction have antiproliferative and anti-inflammatory properties. With 57 distinct
Ajit Dhananjay Jagtap et al.
European journal of medicinal chemistry, 85, 268-288 (2014-08-05)
A series of 6-acylureido derivatives containing a 3-(pyrrol-2-ylmethylidene)indolin-2-one scaffold were synthesized as potential dual Aurora B/FLT3 inhibitors by replacing the 6-arylureido moiety in 6-arylureidoindolin-2-one-based multi-kinase inhibitors. (Z)-N-(2-(pyrrolidin-1-yl)ethyl)-5-((6-(3-(2-fluoro-4-methoxybenzoyl)ureido)-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide (54) was identified as a dual Aurora B/FLT3 inhibitor (IC50 = 0.4 nM and 0.5 nM, respectively).
Lu Li et al.
ACS nano, 9(11), 11342-11350 (2015-09-29)
The next generation of deformable and shape-conformable electronics devices will need to be powered by batteries that are not only flexible but also foldable. Here we report a foldable lithium-sulfur (Li-S) rechargeable battery, with the highest areal capacity (∼3 mAh
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