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N-Methyl-2-pyrrolidone

From Wikipedia, the free encyclopedia
N-Methyl-2-pyrrolidone
Names
Preferred IUPAC name
1-Methylpyrrolidin-2-one
Other names
1-Methyl-2-pyrrolidone
N-Methylpyrrolidone
N-Methylpyrrolidinone
Pharmasolve
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.011.662 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3 checkY
    Key: SECXISVLQFMRJM-UHFFFAOYSA-N checkY
  • InChI=1/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3
    Key: SECXISVLQFMRJM-UHFFFAOYAL
  • CN1CCCC1=O
Properties
C5H9NO
Molar mass 99.133 g·mol−1
Density 1.028 g/cm3
Melting point −24 °C (−11 °F; 249 K)
Boiling point 202 to 204 °C (396 to 399 °F; 475 to 477 K)
Miscible [1]
Solubility in Ethanol, acetone, diethylether, ethyl acetate, chloroform, benzene Soluble[1]
log P −0.40[2]
Hazards
NFPA 704 (fire diamond)
Flash point 91 °C (196 °F; 364 K)[1]
245 °C (473 °F; 518 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

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. It is used in the petrochemical, polymer and battery industries as a solvent, exploiting its nonvolatility and ability to dissolve diverse materials (including polyvinylidene difluoride, PVDF).[3] It has a strong dipole moment and hydrogen bonding due to its cis-amide conformation.[4] : Fig. 5(b) 

Preparation

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NMP is produced industrially by a typical ester-to-amide conversion, by treating gamma-butyrolactone with methylamine. Alternative routes include the partial hydrogenation of N-methylsuccinimide and the reaction of acrylonitrile with methylamine followed by hydrolysis. About 200,000 to 250,000 tons are produced annually.[3]

Applications

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NMP is used to recover certain hydrocarbons generated in the processing of petrochemicals, such as the recovery of 1,3-butadiene and acetylene. Its good solvency properties have also led to NMP's use to dissolve a wide range of polymers. Specifically, it is used as a solvent for surface treatment of textiles, resins, and metal coated plastics or as a paint stripper. It is also used as a solvent in the commercial preparation of polyphenylene sulfide. NMP is used in the production of aramid fibers Twaron and Kevlar. In the pharmaceutical industry, N-methyl-2-pyrrolidone is used in the formulation for drugs by both oral and transdermal delivery routes.[5] It is also used heavily in lithium ion battery fabrication, as a solvent for electrode preparation, because NMP has a unique ability to dissolve polyvinylidene fluoride binder.

Purisol process

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In the Purisol process, developed by Lurgi AG in the 1960s, a cold (ca. -15 °C) aqueous solution of NMP is used to remove hydrogen sulfide from sour gas and from hydrodesulfurization facilities.[6] It offers some advantages over the Selexol process in that it is more selective for hydrogen sulfide. Furthermore, it promotes the hydrolysis of some carbonyl sulfide, a common component of sour gas:

COS + H2O → CO2 + H2S

This hydrolysis step further enriches the hydrogen sulfide content of the off-gas when the NMP is stripped. The sulfur-rich gas is well suited for a Claus unit, which affords solid elemental sulfur.[7]

Safety

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N-Methyl-2-pyrrolidone (NMP) is classified as a reproductive toxicant (H360D: May damage the unborn child) and can cause skin and eye irritation and respiratory irritation (H315, H319, H335).[8] Studies show NMP exposure can increase the risk of developmental toxicity, including miscarriage and fetal death.[9] [10] : 24  Good ventilation and PPE are recommended for safe handling.[11]

See also

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References

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  1. ^ a b c d Sigma-Aldrich Co., 1-Methyl-2-pyrrolidinone. Retrieved on 22 March 2022.
  2. ^ "N-Methylpyrrolidone_msds".
  3. ^ a b Harreus, Albrecht Ludwig; Backes, R.; Eichler, J.-O.; Feuerhake, R.; Jäkel, C.; Mahn, U.; Pinkos, R.; Vogelsang"2-Pyrrolidone, R. (2011). Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_457.pub2. ISBN 978-3-527-30673-2.{{cite encyclopedia}}: CS1 maint: numeric names: authors list (link)
  4. ^ Chenault, H. Keith (2021), "Introduction to Pyrrolidone and Caprolactam Chemistry", Handbook of Pyrrolidone and Caprolactam Based Materials, John Wiley & Sons, Ltd, pp. 1–69, doi:10.1002/9781119468769.hpcbm001, ISBN 978-1-119-46876-9 , retrieved 2025年01月08日
  5. ^ "Pharmasolve® Drug Solubilizer" (PDF). PharmaGuide. International Specialty Products, a division of Ashland Inc.: Page 9. Retrieved 2012年06月06日.
  6. ^ Kohl, Arthur L.; Nielsen, Richard (1997年08月28日). Gas Purification. Elsevier. pp. 1210–1211. ISBN 978-0-08-050720-0.
  7. ^ Boll, Walter; Hochgesand, Gerhard; Higman, Christopher; Supp, Emil; Kalteier, Peter; Müller, Wolf-Dieter; Kriebel, Manfred; Schlichting, Holger; Tanz, Heiner (2011). "Gas Production, 3. Gas Treating". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.o12_o02. ISBN 978-3-527-30385-4.
  8. ^ "Sigma-Aldrich NMP Safety Data Sheet". Sigma-Aldrich. Retrieved October 15, 2024.
  9. ^ "Regulation of Certain Uses under Toxic Substances Control Act: Methylene Chloride and N-Methylpyrrolidone". Environmental Protection Agency. January 19, 2017. EPA-HQ-OPPT-2016-0231-0001. Retrieved October 15, 2024.
  10. ^ "Risk Evaluation for n-Methylpyrrolidone (2-Pyrrolidinone, 1-Methyl-) (NMP)" (PDF). Environmental Protection Agency . December 22, 2020. Archived from the original (PDF) on October 2, 2024. Retrieved January 11, 2025.
  11. ^ "JMNSpecialties NMP Safety Data Sheet". JMNSpecialties. Retrieved October 15, 2024.

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