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Merck
CN

78769

1-甲基-2-吡咯烷酮

analytical standard

别名:

N-甲基-2-吡咯烷酮, N-甲基吡咯烷酮, NMP

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关于此项目

经验公式（希尔记法）:
C5H9NO
化学文摘社编号:
872-50-4
分子量:
99.13
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329768179
EC Number:
212-828-1
Beilstein/REAXYS Number:
106420
MDL number:
MFCD00003193

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产品名称

1-甲基-2-吡咯烷酮, analytical standard

InChI key

SECXISVLQFMRJM-UHFFFAOYSA-N

InChI

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

SMILES string

CN1CCCC1=O

grade

analytical standard

vapor density

3.4 (vs air)

vapor pressure

0.29 mmHg ( 20 °C)
0.99 mmHg ( 40 °C)

assay

≥99.9% (GC)

autoignition temp.

518 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

9.5 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.47 (lit.)
n20/D 1.470

bp

202 °C (lit.)
81-82 °C/10 mmHg (lit.)

mp

−24 °C (lit.)

density

1.028 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

100

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相关类别

Application

1-甲基-2-吡咯烷酮可用作洗脱剂和提取溶剂，用于通过尺寸排阻色谱提取土壤样品中的可溶性物质。
有关合适仪器技术的更多信息，请参考产品′分析证书。如需进一步支持，请联系技术服务部门。

General description

1-甲基-2-吡咯烷酮胺是一种在有机化学和聚合物化学领域中广泛使用的极性溶剂。它被大规模地应用于乙炔、烯烃和二烯烃的回收和纯化，气体纯化和原料芳香化合物提取。
这种物质被列入EU第10/2011号法规中用于与食品接触的塑料的正面清单。10/2011号清单所列全部化合物的标准物质见此
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

存储类别

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

wgk

WGK 1

flash_point_f

195.8 °F - Pensky-Martens closed cup

flash_point_c

91 °C - Pensky-Martens closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCK9544
BCCG9445
BCBZ9275
BCBT7301

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Bioisosteric replacement of acylureido moiety in 6-acylureido-3-pyrrolylmethylidene-2-oxoindoline derivatives resulted in a series of malonamido derivatives with indolin-2-one scaffold (11-14). Further conformational restrictions of the malonamido moiety led to 2-oxo-1,2-dihydropyridine (21-25) or a 4-oxo-1,4-dihydropyridine derivatives (31-36). 4-Oxo-1,4-dihydropyridine derivatives were more potent
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我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

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