4,4'-Methylenedianiline (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "4,4'-Methylenedianiline" in English language version.

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cdc.gov

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0415". National Institute for Occupational Safety and Health (NIOSH).
"4,4'-Methylenedianiline". NIOSH Pocket Guide on Chemical Hazards.

wwwn.cdc.gov

"ToxFAQs for 4,4'-Methylenedianiline". Agency for Toxic Substances and Disease Registry.

dguv.de

gestis.dguv.de

Record of 4,4'-Diaminodiphenylmethane in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 12 February 2021.

doi.org

Endo T, Higashihara T (2022). "Direct Synthesis of Thermally Stable Semiaromatic Polyamides by Bulk Polymerization Using Aromatic Diamines and Aliphatic Dicarboxylic Acids". ACS Omega. 7 (10): 8753–8758. doi:10.1021/acsomega.1c06983. PMC 8928493. PMID 35309482.
Schoustra S, De Heer Kloots M, Posthuma J, Van Doorn D, Dijksman J, Smulders M (2022). "Raman Spectroscopy Reveals Phase Separation in Imine-Based Covalent Adaptable Networks". Macromolecules. 55 (23): 10341–10355. Bibcode:2022MaMol..5510341S. doi:10.1021/acs.macromol.2c01595. PMC 9753755. PMID 36530523.
Roose P, Eller K, Henkes E, Rossbacher R, Höke H (2005). "Amines, Aliphatic". Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001. ISBN 3-527-30673-0.
Chisca D, Croitor L, Melnic E, Petuhov O, Kulikova O, Fonari MS (2020). "Six transition metal–organic materials with the ditopic 4,4′-diaminodiphenylmethane ligand: Synthesis, structure characterization and luminescent properties". Polyhedron. 192: 114844. doi:10.1016/j.poly.2020.114844.
Kopelman H, Robertson MH, Sanders PG, Ash I (February 1966). "The Epping jaundice". British Medical Journal. 1 (5486): 514–6. doi:10.1136/bmj.1.5486.514. PMC 1843808. PMID 5902696.

europa.eu

echa.europa.eu

"Data on manufacture, import, export, uses and release of 4-4' diaminodiphenylmethane" (PDF). Archived from the original (PDF) on 2011-10-01.
"Background document for 4,4'-Diaminodiphenylmethane (MDA)" (PDF). European Chemicals Agency. Archived from the original (PDF) on 2017-08-22. Retrieved 2015-02-24.

harvard.edu

ui.adsabs.harvard.edu

Schoustra S, De Heer Kloots M, Posthuma J, Van Doorn D, Dijksman J, Smulders M (2022). "Raman Spectroscopy Reveals Phase Separation in Imine-Based Covalent Adaptable Networks". Macromolecules. 55 (23): 10341–10355. Bibcode:2022MaMol..5510341S. doi:10.1021/acs.macromol.2c01595. PMC 9753755. PMID 36530523.

nih.gov

ncbi.nlm.nih.gov

Endo T, Higashihara T (2022). "Direct Synthesis of Thermally Stable Semiaromatic Polyamides by Bulk Polymerization Using Aromatic Diamines and Aliphatic Dicarboxylic Acids". ACS Omega. 7 (10): 8753–8758. doi:10.1021/acsomega.1c06983. PMC 8928493. PMID 35309482.
Schoustra S, De Heer Kloots M, Posthuma J, Van Doorn D, Dijksman J, Smulders M (2022). "Raman Spectroscopy Reveals Phase Separation in Imine-Based Covalent Adaptable Networks". Macromolecules. 55 (23): 10341–10355. Bibcode:2022MaMol..5510341S. doi:10.1021/acs.macromol.2c01595. PMC 9753755. PMID 36530523.
Kopelman H, Robertson MH, Sanders PG, Ash I (February 1966). "The Epping jaundice". British Medical Journal. 1 (5486): 514–6. doi:10.1136/bmj.1.5486.514. PMC 1843808. PMID 5902696.

pubmed.ncbi.nlm.nih.gov

Endo T, Higashihara T (2022). "Direct Synthesis of Thermally Stable Semiaromatic Polyamides by Bulk Polymerization Using Aromatic Diamines and Aliphatic Dicarboxylic Acids". ACS Omega. 7 (10): 8753–8758. doi:10.1021/acsomega.1c06983. PMC 8928493. PMID 35309482.
Schoustra S, De Heer Kloots M, Posthuma J, Van Doorn D, Dijksman J, Smulders M (2022). "Raman Spectroscopy Reveals Phase Separation in Imine-Based Covalent Adaptable Networks". Macromolecules. 55 (23): 10341–10355. Bibcode:2022MaMol..5510341S. doi:10.1021/acs.macromol.2c01595. PMC 9753755. PMID 36530523.
Kopelman H, Robertson MH, Sanders PG, Ash I (February 1966). "The Epping jaundice". British Medical Journal. 1 (5486): 514–6. doi:10.1136/bmj.1.5486.514. PMC 1843808. PMID 5902696.

web.archive.org

"Data on manufacture, import, export, uses and release of 4-4' diaminodiphenylmethane" (PDF). Archived from the original (PDF) on 2011-10-01.
"Background document for 4,4'-Diaminodiphenylmethane (MDA)" (PDF). European Chemicals Agency. Archived from the original (PDF) on 2017-08-22. Retrieved 2015-02-24.