|Related Categories||Alkaloid, Asymmetric Synthesis, Bioactive Small Molecules, Cell Biology, Chemical Synthesis,|
|optical activity||[α]20/D −41°, c = 7 in 1 M HCl|
|Gene Information||rat ... Adra1a(29412), Adra1b(24173), Adra1d(29413)|
10, 50 g in glass bottle
Certificate of Analysis
|Precautionary statements||P261-P305 + P351 + P338|
|Personal Protective Equipment||dust mask type N95 (US), Eyeshields, Gloves|
|Hazard Codes (Europe)||Xn|
|Risk Statements (Europe)||22-36/37/38|
|Safety Statements (Europe)||26|
|Flash Point(F)||235.4 °F|
|Flash Point(C)||113 °C|
Both enantiomers of ephedrine, pseudoephedrine, norephedrine, and their derivatives are used as practical chiral auxiliaries for asymmetric synthesis. Enolates of readily available (1R,2R)-(–)- and (...
Aldrich ChemFiles 2005, 5.4, 9.
Keywords: Alkylations, Asymmetric synthesis, Chiral auxiliaries
Simultaneous identification of the enantiomers and diastereomers of N,O-di-trifluoroacetylated ephedrine and norephedrine in blood plasma using chiral capillary gas chromatography-mass spectrometry with selected ion monitoring. Nagai T, Kurosu A, Matsushima K, et al. J. Anal. Toxicol. 36(2), 96-105, (2012)
Determination of the active principles of Catha Edulis: quali-quantitative analysis of cathinone, cathine, and phenylpropanolamine. Gambaro V, Arnoldi S, Colombo ML, et al. Forensic Sci. Int. 217(1-3), 87-92, (2012)
Development of a liquid chromatography tandem mass spectrometry method for simultaneous determination of eight adulterants in slimming functional foods. Shi Y, Sun C, Gao B, et al. J. Chromatogr. A 1218(42), 7655-62, (2011)
Determination of urinary concentrations of pseudoephedrine and cathine after therapeutic administration of pseudoephedrine-containing medications to healthy subjects: implications for doping control analysis of these stimulants banned in sport. Barroso O, Goudreault D, Carbó Banús ML, et al. Drug Test. Anal. 4(5), 320-9, (2012)
Comparison of contents of five ephedrine alkaloids in three official origins of Ephedra Herb in China by high-performance liquid chromatography. Hong H, Chen HB, Yang DH, et al. J. Nat. Med. 65(3-4), 623-8, (2011)
The relevance of the urinary concentration of ephedrines in anti-doping analysis: determination of pseudoephedrine, cathine, and ephedrine after administration of over-the-counter medicaments. Strano-Rossi S, Leone D, de la Torre X, et al. Ther. Drug Monit. 31(4), 520-6, (2009)
Stereoselective synthesis of norephedrine and norpseudoephedrine by using asymmetric transfer hydrogenation accompanied by dynamic kinetic resolution. Lee HK, Kang S, and Choi EB J. Org. Chem. 77(12), 5454-60, (2012)
Cathine, an amphetamine-related compound, acts on mammalian spermatozoa via beta1- and alpha2A-adrenergic receptors in a capacitation state-dependent manner. Adeoya-Osiguwa SA and Fraser LR Hum. Reprod. 22(3), 756-65, (2007)
Fieser 12,338 / Fieser 13,200 / Fieser 14,215
Corp MSDS 1 (2), 2624:B / FT-IR 2 (2), 2154:D / FT-NMR 1 (2), 577:A / RegBook 1 (1), 1469:K / Structure Index 1, 229:B:8
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Need larger quantities for your development, manufacturing or research applications?