SUBJECT INDEX 



927 



Cholesteiyl acetate (co)itmned) 

 specific rotation, 330 

 structure, 334 



Cholestery 

 Cholestery 

 Cholosiory 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestero 

 Chole.stery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholesterj' 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholesterj' 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 

 Cholestery 



wax, 366 



Cholestery 



allophanat(\ 332 

 benzoate, 332 

 butyrate, constants, 330 

 caprate, constants, 330 

 caproate, constants, 330 

 caprylate, constants, 330 

 diadipate, constants, 331 

 dibromide, properties, 333 

 diglutarate, constants, 331 

 dioxalate, constants, 331, 332 

 disuberate, constants, 331 

 disuccinate, constants, 331 

 elaidate, constants, 331 

 erucate, constants, 331 

 formate, constants, 330 

 isobutyrate, constants, 330 

 isovalerate, constants, 330 

 laurate, constants, 330 

 lignocerate, constants, 330 

 linoleate, constants, 331 

 linolenate, constants, 331 

 mono-adipate, constants, 331 

 mono-oxalate, constants, 331 

 monosuberate, constants, 331 

 monosuccinate, 331 

 myristate, constants, 330, 332 

 oleate, constants, 329, 330 

 palmitate, constants, 329, 330 

 palmitoleate, in yellow bees- 



petroselinate, solubility, 331 



specific rotation, 331 

 Cholesteryl propionate, constants, 330 

 Cholestery 1 stearate, constants, 329, 330 

 Cholesteryl undecenoate, constants, 330 

 Cholesteryl valerate, constants, 330 

 Choline, 426-432 



acptylcholino formation. 428 



distribution, 427, 428 



from sphingomyelin, 460 



methods for determination. 429-432 



properties, 428, 429 



synthesis, 427 

 Choline acetylase, 428 

 C'holine esterase, 428 

 Choline reineckate, 429-431 

 Christmas berrj'' leaves, carotene in, 518 

 Chromans and vitamin E biopotency, 823 

 Chromatographic separation of fatty 

 acids. 183 



Chromatography, 652-661 



applications, 653, 654 



caiotenoids and, 660 



historical, 652, 653 



procedures, 655-659 



structure and adsorption, 659 



theory, 654, 655 

 Chromene derivatives and vitamin E 



biopotency, 823, 824 

 Chromolipoids, 512 

 Chrysanthemaxanthin, 568-570 



absorption spectra, 610 



properties, 604 

 Chrysene, from cholesterol, 336 



structure, 323 

 Chrysophyll, 511 

 Cinnamon oil, composition, 205 

 (v.s-Linkages, position of Xmax. and, 650, 



651 

 cis-Peak effect, 644-650 



development, 645, 647 



extinction, 648 

 cis-lranf; Isomerization (see also Stereo- 

 isomers) 



by acid catalysis, 636 



by iodine catalysis, 635 



by melting crystalline carotenoids, 632 



by photochemical action, 637 



by refluxing solutions, 633 



in polyenes, 625 

 a-Citraurin, 561 



possible stereoisomers, 627 

 /3-Citraurin, 580, 581 



possible stereoisomers, 627 

 Citric acid, as inhibitol synergist, 297 

 Clarit as adsorbent, 658 

 CUonasterol, 347 



Clothes moth, vitamin A and, 677 

 Cloudberry, rubixanthin in, 553 

 Clupanodonic acid, as component of 

 lecithin, 424, 425 



discovery, 19 



physical constants, 47 

 Cobra venom, lysocephalin and, 444, 445 



lysolecithin and, 414, 419 

 Cocaine tree, lycopene in, 544 

 Cocceric acid, in plant bark waxes, 379 

 Coccerin, saponification, 363 

 Cocceryl alcohol, 311 

 Cochineal wax, 15-keto-n-tetratriacon- 



tanol from, 311 

 Cockchafer beetle, cholesterol in, 327 



