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  • phosphine
  • They are generated by the reaction of phosphine with formaldehyde in the presence of the mineral acid: PH3 + HX + 4 CH2O → [P(CH2OH)4+]X− A variety of phosphonium salts can be prepared by alkylation and arylation of organophosphines: PR3 + R'X → [PR3R'+]X− The methylation of triphenylphosphine is the first step in the preparation of the Wittig reagent. (wikipedia.org)
  • structure
  • Fraction sorbed to airborne particulates (phi): 0.999 (Junge,Mackay) Note: the sorbed fraction may be resistant to atmospheric oxidation Soil Adsorption Coefficient (PCKOCWIN v1.66): Koc : 26.53 Log Koc: 1.424 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1. Rate constants can NOT be estimated for this structure! (chemspider.com)
  • solution
  • 10. The method in accordance with claim 1 wherein said acid comprises a solution having a concentration ranging from about 0.001 molar to a saturated solution of said organic phosphorus-containing compound. (patentgenius.com)
  • treatment
  • Fosfomycin aka: (1R,2S)-Epoxypropylphosphonic acid It is used for the treatment of acute cystitis (urinary tract infections) and gastrointestinal infections. (wikibooks.org)