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N-Methyl-2-pyrrolidone (NMP) is an organic compound consisting of a 5-membered lactam. It is a colorless liquid, although impure samples can appear yellow. It is miscible with water and with most common organic solvents. It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide.
2-Pyrrolidone, also known as 2-pyrrolidinone or butyrolactam, is an organic compound consisting of a 5-membered lactam, making it the simplest γ-lactam. It is a colorless liquid that is miscible with water and most common organic solvents.
CH 3 N(C 2 H 4 OH) 2: methyl diethanolamine: 105-59-9 CH 3 NC: methyl isocyanide: 593-75-9 C 5 H 9 NO: N-Methyl-2-pyrrolidone: 872-50-4 CH 3 CH 2 CH 2 OH: 1-Propanol: 71-23-8 CH 2 (CH 2 OH) 2: 1,3-Propanediol: 504-63-2 HOCH 2 CH 2 CH 2 CH 2 CH 2 OH: 1,5-Pentanediol: 111-29-5 (CH 3) 2 CHOH: 2-Propanol: 67-63-0 CH 3 CH 2 COOH: propanoic acid: 79 ...
It is a colourless liquid that is miscible with water and most organic solvents. It has a characteristic odor that has been described as "ammoniacal, fishy, shellfish-like". [ 4 ] In addition to pyrrolidine itself, many substituted pyrrolidines are known.
Gamma-Butyrolactone is used as a chemical solvent and a cleaning agent, [15] for example in paint stripping or for cleaning graffiti. [16] Butyrolactone is a precursor to other chemicals. Reaction with methylamine gives NMP, and with ammonia gives pyrrolidone. It is also used as a solvent in lotions and some polymers. [5]
Aromatic polyamides (e.g. Kevlar and Nomex) are made by polycondensation in N-methyl-pyrrolidone and calcium chloride solution. This process is one of two used in the production of sodium polyacrylate, a superabsorbent polymer used in disposable diapers.
N-Vinylpyrrolidone (NVP) is an organic compound consisting of a 5-membered lactam ring linked to a (2 carbon) vinyl group. It is a colorless liquid although commercial samples can appear yellowish. It is produced industrially by vinylation of 2-pyrrolidone, i.e. the base-catalyzed reaction with acetylene. [2]
This page was last edited on 12 November 2012, at 01:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
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