Lyons, John H.; Little, Steven M.; Esposito, Vincent J. (1976-01-20) "Chemiluminescent signal device" U.S. Patent 3,933,118 Rempfer, Kyle (2019-02-21). "Air Force labs develop and field chemlight replacement". Air Force Times . Retrieved 2021-10-04. Nyoka was started to create a completely non-toxic, biodegradable light source based on bioluminescence that is not only safe for people and the planet, but helps to restore some of the damage. a b Kuntzleman, Thomas S.; Comfort, Anna E.; Baldwin, Bruce W. (2009). "Glowmatography". Journal of Chemical Education. 86 (1): 64. Bibcode: 2009JChEd..86...64K. doi: 10.1021/ed086p64.

Mohan, Arthur G. and Rauhut, Michael M. (1983-04-05) "Chemical lighting device" U.S. Patent 4,379,320 BASED IN THE USA| We're proud to be a US-based, family-owned company in business since 1981. Our passion is to always provide you with the best selection of unique gifts and novelties. Rauhut, Michael M. (1969). "Chemiluminescence from concerted peroxide decomposition reactions (science)". Accounts of Chemical Research. 2 (3): 80–87. doi: 10.1021/ar50015a003.The Wand itself is infinitely reusable, and the glow is created with non-toxic bioluminescent enzymes. Just add water and shake to glow! chloro-9,10-diphenylanthracene (1-chloro(DPA)) and 2-chloro-9,10-diphenylanthracene (2-chloro(DPA)) emit blue-green light more efficiently than nonsubstituted DPA Chandross, Edwin A. (1963). "A new chemiluminescent system". Tetrahedron Letters. 4 (12): 761–765. doi: 10.1016/S0040-4039(01)90712-9. Rood, S. A. "Chapter 4 Post-Legislation Cases" (PDF). Government Laboratory Technology Transfer: Process and Impact Assessment (Doctoral Dissertation). hdl: 10919/30585. Archived from the original on 2015-10-26 . Retrieved 2020-09-23.

a b c d Bindra, Perminder S.; Burris, Andrew D.; Carlson, Carl R.; Smith, Joann M.; Tyler, Orville Z. and Watson, David L. Jr. (2010-03-09) "Chemiluminescent compositions and methods of making and using thereof" U.S. Patent 20,080,308,776 Bis(2,4,5-trichlorophenyl-6-carbopentoxyphenyl)oxalate, trademarked "Cyalume", was invented in 1971 by Michael M. Rauhut, [1] of American Cyanamid, based on work by Edwin A. Chandross and David Iba Sr. of Bell Labs. [2] [3] Clark, Donald E. "Peroxides and Peroxide Forming Compounds" (PDF). bnl.gov. Texas A&M University . Retrieved 2019-12-15. di-tert-butylphenyl 1,4,5,8-tetracarboxynaphthalene diamide emits deep red light, together with DPA is used to produce white or hot-pink light, depending on their ratioDavies, D (1998). "Diver location devices". Journal of the South Pacific Underwater Medicine Society. 28 (3). Archived from the original on 2009-05-19.