Користувач:Rimas v/budmaidan
| Метилпіролідон | |
|---|---|
| |
| Систематична назва | 1-Метилпіролідин-2-он |
| Якщо не зазначено інше, дані наведено для речовин у стандартному стані (за 25 °C, 100 кПа) | |
| Інструкція з використання шаблону | |
| Примітки картки | |
N-Метил-2-піролідон — хімічна сполука with 5-membered lactam structure. It is a clear to slightly yellow liquid miscible with water and solvents like ethyl acetate, chloroform, benzene and lower alcohols or ketones. It also belongs to the class of dipolar aprotic solvents which includes also dimethylformamide, dimethylacetamide and dimethyl sulfoxide. Other names for this compound are: 1-methyl-2-pyrrolidone, N-methyl-2-pyrrolidinone, and m-pyrrole, and pharmasolve.
N-Methylpyrrolidone is used to recover pure hydrocarbons while processing petrochemicals and in the desulfurization of gases. Due to its good solvency properties N-methyl-2-pyrrolidone is used to dissolve a wide range of chemicals, especially in the polymers field. It also used as a solvent for surface treatment of textiles, resins and metal coated plastics or as a paint stripper.[1] In the pharmaceutical industry, N-methyl-2-pyrrolidone is used in the formulation for drugs by both oral and transdermal delivery routes.[2] Furthermore, small amounts of N-Methyl-2-pyrrolidone are contained in various medical devices like self-hardening bone graft substitutes, dental barrier membranes and subcutaneous drug delivery devices.
N-Methyl-2-pyrrolidone and its derivatives are used as intermediates for the synthesis of agrochemicals, pharmaceuticals, textile auxiliaries, plasticizers, stabilizers and specialty inks. It is also employed as a nylon precursor. The rubber industry uses it for SBR latex production and the electronics industry for printed circuit board manufacturing.[1] NMP is also used in lithium cell creation.
World production capacity for NMP was 226 million lb in 2006. NMP has desirable properties such as low volatility, low flammability, and relatively low toxicity. However, it has been identified as a reproductive toxicant, first by California in 2001 and then by the European Commission in 2003. In the face of increasing regulation, some manufacturers are considering alternative solvents for some applications, especially where worker exposure is difficult to control, such as in paint stripping and agriculture.[3]
See also ред.
References ред.
- ↑ а б Products: N-Methylpyrrolidone. BASF. Процитовано 11 листопада 2007.
- ↑ "Pharmasolve" (PDF). International Specialty Products. Процитовано 15 квітня 2008.
- ↑ Reisch, Mark (21 липня 2008). Solvent users look to replace NMP. Chemical & Engineering News: 32.