328634
NMP
anhydrous, 99.5%
Synonym(s):
1-Methyl-2-pyrrolidone, N-Methyl-2-pyrrolidone, NMP
About This Item
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product name
1-Methyl-2-pyrrolidinone, anhydrous, 99.5%
grade
anhydrous
Quality Level
vapor density
3.4 (vs air)
vapor pressure
0.29 mmHg ( 20 °C)
0.99 mmHg ( 40 °C)
Assay
99.5%
form
liquid
autoignition temp.
518 °F
expl. lim.
9.5 %
impurities
<0.005% water
refractive index
n20/D 1.47 (lit.)
pH
7.7-10.0 (20 °C, 100 g/L)
bp
202 °C (lit.)
81-82 °C/10 mmHg (lit.)
mp
−24 °C (lit.)
density
1.028 g/mL at 25 °C (lit.)
SMILES string
CN1CCCC1=O
InChI
1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3
InChI key
SECXISVLQFMRJM-UHFFFAOYSA-N
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Application
- Preparation of 2-aryl and 2-alkyl benzothiazoles.
- Ullmann coupling reaction of aryl halides and phenols to form Ullmann ethers in the presence of 2,2,6,6-tetramethylheptane-3,5-dione.
- Stille cross-coupling reaction of aryl iodides with organostannanes catalyzed by Pd/C in the presence of copper iodide as cocatalyst.
Packaging
Other Notes
Legal Information
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suggested gloves for splash protection
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 1
Personal Protective Equipment
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Amide bonds are ubiquitous in both nature and industrial applications. They are vital to the structure and function of biological macromolecules and polymers. The importance of this functionality has resulted in numerous approaches to its formation, ranging from stoichiometric activation of carboxylic acids to more recent advances in catalytic amide bond formation.
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