|
You will need |
Capsaicin: C18H27NO3 (E)-N-[(4-hydroxy-3-methoxyphenyl)-methyl] -8-methyl-6-noneamide Trade Names: Axsain; Mioton; Zostrix Monoclinic, retangular plates MW 305.42, MP 65o C, BP0.01 210-220oC Pungent principle in various species of Capsicum, Solanaceae. Isolated from cayenne and paprika. Capsaicin is a powerful irritant; initial administration causes intense pain. Prolonged treatment causes insensitivity to painful stimuli and induces selective degeneration of some primary sensory neurons. Burning taste, one part in 100,000 can be detected by tasting. Practically insoluble in water. Freely soluble in alcohol. USE: As a tool in neurobiological research. Preliminary clinical evaluation in chronic postherpetic neuralgia. J.E. Bernstein et al., J American Academy of Dermatology, Volume 17, page 93, 1987 |
1850 - 1936
1627 - 1691 |
The CRC Handbook of Chemistry and Physics The Merck Index Excel Spreadsheet Tutor Excel Graphing Tutor Molecular Mass Calculator (Will calulate the mass and percent composition of a molecular species) Balancing Redox Equations (a tutorial in Power Point, once powerpoint launches press the F5 key. If you do not have powerpoint download the powerpoint viewer, download and save the file and launch it with the viewer.) The Periodic Table A Short History JT Baker Chemicals or Sigma-Aldrich (catalog search engines of chemicals. This is where I go to download Material Safety Data Sheets) University of Vermont SIRI (I also use this one for MSDS information) Mega Converter (This will convert anything) Texas A&M Section of the American Chemical Society |