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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 itself is used in inkjet cartridges. [5] A variety of pharmaceutical drugs are 2-pyrrolidone derivatives, including cotinine, doxapram, povidone, and ethosuximide, and the racetams. The chemical is an intermediate in the production of the polyvinylpyrrolidone precursor vinylpyrrolidone. [3]
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N1-Methyl-2-pyridone-5-carboxamide (also known as 1-methyl-6-oxopyridine-3-carboxamide or nudifloramide and abbreviated as 2PY, 2-Py or NMPC) is one of a number of metabolic products of nicotinamide adenine dinucleotide (NAD) degradation.
Pyrrolidine, also known as tetrahydropyrrole, is an organic compound with the molecular formula (CH 2) 4 NH. It is a cyclic secondary amine , also classified as a saturated heterocycle . It is a colourless liquid that is miscible with water and most organic solvents.
They show a lot if information about the chemical structures and what they might be used for etc, but very often nothing about where they come from and what they are made from. This chemical N-Methyl-2-pyrrolidone is a prime example where there is nothing give anywhere on the page how it is made or what from.
It has a low vapor pressure, and is nearly odorless. [2] It has a low solubility in water, but is soluble in a variety of organic solvents. CHP is used in the electronics industry as a photoresist stripper (usually in combination with other solvents like N-methyl-2-pyrrolidone), and as a chemical polisher of copper in circuit board fabrication. [3]
N-Methylmorpholine is the organic compound with the formula O(CH 2 CH 2) 2 NCH 3. It is a colorless liquid. It is a cyclic tertiary amine. It is used as a base catalyst for generation of polyurethanes and other reactions. It is produced by the reaction of methylamine and diethylene glycol as well as by the hydrogenolysis of N-formylmorpholine. [2]