4-Nitroaniline (English Wikipedia)

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

refsWebsite

Global rank English rank

6doi.org

2^nd place

3orgsyn.org

2,971^st place

2,826^th place

2cdc.gov

218^th place

212^th place

2wiley.com

222^nd place

297^th place

1web.archive.org

1^st place

1centre.edu

low place

1archive.org

6^th place

1ed.gov

576^th place

352^nd place

1acs.org

1,248^th place

1,104^th place

1youtube.com

9^th place

13^th place

1sigmaaldrich.com

924^th place

2,352^nd place

acs.org

communities.acs.org

"Carbon Snake: demonstrating the dehydration power of concentrated sulfuric acid". communities.acs.org. 2013-06-06. Retrieved 2022-01-31.

archive.org

Williamson, Kenneth L. (2002). Macroscale and Microscale Organic Experiments, Fourth Edition. Houghton-Mifflin. ISBN 0-618-19702-8.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0449". National Institute for Occupational Safety and Health (NIOSH).
"p-Nitroaniline". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

centre.edu

web.centre.edu

Mohrig, J.R.; Morrill, T.C.; Hammond, C.N.; Neckers, D.C. (1997). "Synthesis 5: Synthesis of the Dye Para Red from Aniline". Experimental Organic Chemistry. New York, NY: Freeman. pp. 456–467. Archived from the original on 2020-09-15. Retrieved 2007-07-18.

doi.org

Booth, Gerald (2003-03-11). "Nitro Compounds, Aromatic". In Wiley-VCH (ed.). Ullmann's Encyclopedia of Industrial Chemistry (1 ed.). Wiley. doi:10.1002/14356007.a17_411. ISBN 978-3-527-30385-4.]
Starkey, E. B. (1939). "p-DINITROBENZENE". Organic Syntheses. 19: 40. doi:10.15227/orgsyn.019.0040.
Ruddy, A. Wayne; Starkey, Edgar B. (1946). "p-Nitrophenylarsonic Acid". Organic Syntheses. 26: 60. doi:10.15227/orgsyn.026.0060.
Shriner, R. L.; Horne, W. H.; Cox, R. F. B. (1934). "p-NITROPHENYL ISOCYANATE". Organic Syntheses. 14: 72. doi:10.15227/orgsyn.014.0072.
Sandin, R. B.; Drake, W. V.; Leger, Frank (1932). "2,6-Diiodo-p-Nitroaniline". Organic Syntheses. 12: 28. doi:10.15227/orgsyn.012.0028.
Poshkus, A. C.; Parker, J. A. (1970). "Studies on nitroaniline–sulfuric acid compositions: Aphrogenic pyrostats". Journal of Applied Polymer Science. 14 (8): 2049–2064. doi:10.1002/app.1970.070140813.

ed.gov

eric.ed.gov

Summerlin, Lee R.; Ealy, James L. (1988). "Experiment 100: Dehydration of p-Nitroaniline: Sanke and Puff". Chemical Demonstrations: A Sourcebook for Teachers Volume 1 (2nd ed.). American Chemical Society. p. 171. ISBN 978-0-841-21481-1.

orgsyn.org

Starkey, E. B. (1939). "p-DINITROBENZENE". Organic Syntheses. 19: 40. doi:10.15227/orgsyn.019.0040.
Ruddy, A. Wayne; Starkey, Edgar B. (1946). "p-Nitrophenylarsonic Acid". Organic Syntheses. 26: 60. doi:10.15227/orgsyn.026.0060.
Shriner, R. L.; Horne, W. H.; Cox, R. F. B. (1934). "p-NITROPHENYL ISOCYANATE". Organic Syntheses. 14: 72. doi:10.15227/orgsyn.014.0072.

sigmaaldrich.com

"4-Nitroaniline". St. Louis, Missouri: Sigma-Aldrich. December 18, 2020.

web.archive.org

Mohrig, J.R.; Morrill, T.C.; Hammond, C.N.; Neckers, D.C. (1997). "Synthesis 5: Synthesis of the Dye Para Red from Aniline". Experimental Organic Chemistry. New York, NY: Freeman. pp. 456–467. Archived from the original on 2020-09-15. Retrieved 2007-07-18.

wiley.com

onlinelibrary.wiley.com

Booth, Gerald (2003-03-11). "Nitro Compounds, Aromatic". In Wiley-VCH (ed.). Ullmann's Encyclopedia of Industrial Chemistry (1 ed.). Wiley. doi:10.1002/14356007.a17_411. ISBN 978-3-527-30385-4.]
Poshkus, A. C.; Parker, J. A. (1970). "Studies on nitroaniline–sulfuric acid compositions: Aphrogenic pyrostats". Journal of Applied Polymer Science. 14 (8): 2049–2064. doi:10.1002/app.1970.070140813.

youtube.com

Making a carbon snake with P-Nitroaniline, 7 April 2014, retrieved 2022-01-31