SUBJECT INDEX 



949 



Melting point {continued) : 

 of ergosteryl esters, 359 

 of eschscholtziaxanthin osters, 586 

 Nof hydroxy acids, 48 

 of lutein esters, 559 

 of monoethenoid acids, 46 

 of neovitamin A, 730 

 of polyethenoid acids, 47 

 of provitamins D, 749 

 of saturated acids, 45 

 of sitosterols, 350 

 of sitosterol esters, 350 

 of sphingosine esters, 465 

 of unsaturated monatomic alcohols, 310 

 of vitamin A derivatives, 674, 698 

 of vitamin Ai, 730 

 of vitamin Aa, 730 

 of vitamin A3, 730 

 of vitamin A esters, 730 

 of vitamin D2, 779 

 of vitamin D3, 780 

 of vitamin Dt, 780 

 of zeaxanthin esters, 564 

 polymorphism and, 248-269 

 in diglycerides, 263-266 

 in monoglycerides, 266-269 

 in simple triglycerides, 252-254 

 in symmetrical mixed triglycerides, 



255-259 

 in unsymmetrical mixed triglycerides, 

 259-262 

 in triacid triglycerides, 259, 263 

 position and number of methyl groups 



and, 54-56 

 position of double bonds and, 52 

 refractive index and, 240 

 Menadione, antihemorrhagic action, 831, 

 844-847 

 biopotency, of 2-substituted, 847 



of 3-substituted, 844-846 

 structure, 838 

 Menhaden oil, constants, 236 



vitamins D in, 772 

 Mercury vapor lamp for irradiation, 759 

 Mesomorphic state, 329 

 Metabolized vitamin D milk, 775, 778 

 Methanolysis, 276 

 2-Methoxy-l,4-naphthoquinone, vitamin 



E biopotency, 826 

 Methyl adipate, constants, 121 

 o-[a-Methylallyl]-phenol, vitamin E bio- 

 potency, 825 

 A''-Methyl amides, melting points, 138 



Methylamyl ketone in rancid fats, 284 

 /S-Methj'lanthraquinone, vitamin E bio- 

 potency, 826 

 Methyl arachidonate, absorption spec- 

 trum, 81 

 boiling point. 111, 120 

 density, 120 

 melting point, 120 

 refractive index, 120 

 Methyl azelate, constants, 121 

 Methjd behenate, melting point, 120 

 2-Methyl-3-benzyl-l,4-naphthoquinone, 



vitamin K biopotency, 846 

 Methyl bixin, absorption spectra. 644 

 extinction curve, 618 

 possible stereoisomers, 627 

 Methyl caprate, constants, 111, 120 

 Methyl caproate, constants, 111, 120 

 Methyl caprylate, constants. 111, 120 

 2-Methyl-3-carbethoxy-l,4-naphthohy- 

 droquinone, vitamin K biopotency, 

 850, 851 

 Methyl cerotate, constants, 120 

 Methyl chaulmoograte, boiling point. 111 

 Methylcholanthrene, structure, 322 

 2-Methyl-3-cinnamyl-l,4-naphthoqui- 

 none, vitamin K biopotency, 846 

 2-MethyI-3-cinnamyl-l,4-naphthoquinone 



oxide, vitamin K biopotency, 852 

 Methyl clupanodonate, boiling point, 111 

 2-Methylcoumarin, vitamin E bio- 

 potency, 824 

 3-MethyIcoumarin, vitamin E bio- 

 potency, 824 

 Methyl crocetin, possible stereoisomers, 



627 

 7-Methylcyclopentenophenanthrene, 



from ergosterol, 751 

 2-Methyl-3-difarnesyl-l,4-naphthoqui- 



none (see Vitamin K2) 

 2-Methyl-5,8-dihydro-l,4-naphthohydro- 

 quinone, vitamin K biopotency, 856 

 2-Methyl-3-(/3,7-dihydrophytyl)-l,4- 

 naphthoquinone, vitamin K bio- 

 potency, 846, 851 

 2-Methyldocosanoic acid, 55 

 10-Methyldocosanoic acid, 55 

 2-Methyleicosanoic acid, 55 

 Methyl elaidate, boiling point, 111 

 Methyl erucate, boiling point, 111 

 2-Methyl-4-ethylchroman, vitamin E bio- 

 potency, 823 



