FATTY ACID COMPONENTS OF BLACK RIGHT WHALE OIL BY GAS CHROMATOGRAPHY HIDEO TSUYUKI* AND SHINGO ITOH* INTRODUCTION

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FATTY ACID COMPONENTS OF BLACK RIGHT WHALE OIL BY GAS CHROMATOGRAPHY HIDEO TSUYUKI* AND SHINGO ITOH* INTRODUCTION There have been a number of studies on whale oil. However, there are a few studies on black right whale oil. As to the study on black right whale oil, we can find the following reports; Studies on the oil of black right whale in the Northern Pacific Ocean (Tsuyuki and Naruse, 1963), Studies on the lipids in brain of black right whale in the Northern Pacific Ocean (Tsuyuki and Naruse, 1964), Studies on liver oil of black right whale (Tsuyuki, Naruse, Mochizuki and Itoh, 1964). So far as these works concerned with chemical properties of oils and fatty acid components by fractional distillation, minute examinations of fatty acid components have not been reported yet. So the purpose of the present work is a minute examination of the fatty acid components of black right whale oil by gas-liquid chromatography using a hydrogen ionization detector. It is pleasure that we express here our thanks to Dr. H. Omura and Dr. S. Ohsumi in the Whales Research Institute who were kind enough to present us black right whale oils. MATERIAL AND METHOD Sample used Material is the black right whale, Eubalaena glacial is, (male, body length: 17.1 m, presumed age: more than 1 years old) which was caught at the southern sea of Kodiak Island in the Northern Pacific Ocean in 196 (Tsuyuki and Naruse, 1963). The oils contained in 9 parts of s were obtained by boiling these s with water and those in 3 kinds of organs were extracted with acetone in an atmosphere of nitrogen gas. The oils used in the present report were stocks used in previous reports (Tsuyuki and Naruse, 1963, 1964). The bottles of sample oils have been filled up with nitrogen gas and preserved in refrigerator at low temperature. Used sample oils are the oils contained in 3 kinds of organs (stomach, liver and tongue), and 9 parts of s (middle back, thoracic, abdominal, brain, hind part of blow-hole, umbilicus, anterior abdominal, fore part of genital aperture and posterior back). The properties of 9 oils and 3 organ oils are shown in Table 1. * Department of Food Engineering, College of Agriculture & Veterinary Medicine, Nihon University. Xo., 197, 165-17.

166 TSUYUKI AND ITOH TABLE!. PROPERTIES OF THE OILS CONTAINED IN VARIOUS BLUBBERS AND ORGANS OF BLACK RIGHT WHALE Kinds of and organ Acid value Saponification Iodine value U nsaponifiable value Matter (%) Stomach.8 19.6 131.5 1. Liver.5 9.5 131.4 1.45 Tongue.1 195.4 115.l 1. Middle back 1. 196.6 16.6.77 Thoracic 1.1 191.8 13.8 1.5 Abdominal.7 7.6 13.5.94 Brain 1.1.4 134..8 Blubber of hind part of blow-hole 1.5 194.1 17.1 1.14 Umbilicus 1.6 19.4.6 1.5 Anterior abdominal 1.6 19.7 134.9.8 Blubber of fore part of genital aperture 1.9 193.7 13.6.91 Posterior back 1.8 19. 19.7.7 Preparation of methyl ester of fatty acid The methyl esters of the fatty acids of sample oils were prepared by a semimicro methanolysis adapted to the method of Gauglitz and Lehmann (1963) for use in gas-liquid chromatography analysis. Then, to remove colesterol, coloring materials, impurities and others, the methyl esters were refined by passing through in glass column packed with silicic acid. Gas-liquid chromatograpfry The methyl esters of the fatty acids of the black right whale oils were analyzed with a Shimadzu Gas Chromatograph Apparatus, Model GC-1 C. The instrument was equipped with a hydrogen ionization detector. The column used was composed of 3 mm in diameter by 5 cm U shaped stainless steel column containing % diethylene glycol succinate polyester (DEGS from Shimadzu Seisakusyo Co.) supported on 6-8 mesh Shimalite. Operating conditions were as follows; column temp. 1 C, injector temp. 6 C, detector temp. 4 C. A column inlet pressure of 1.8 kg/cm N was used, which measured 7-74 ml/min. at the flow rate. Each peak was identified by comparing retention time with those in a known mixture of standard fatty acid methyl esters (C 1 to C 4 as saturated fatty acids, and C 16 monoenoic acid and C mono-, di- and trienoic acids as unsaturated fatty acids), and semilogarithmic plots of carbon number vs relative retention time were used for identification by the method of Nelson and Freeman (196). Also, for the purpose of identification of odd carbon chain length fatty acids, the hydrogenation was operated as follows; the n-hexanate solution of methyl esters was added a pinch of palladium on activated carbon as a catalyst. The mixture was shaken in a small flask for 5-6 hours under hydrogen atmosphere (approximate 1.5 kg/cm ) at room temperature, and then filtered. The hydrogenated methyl esters were operated by gas chromatograph at the same condition. No., 197.

;"' "" ""... "' S< "' Fatty acid chain length No. C atoms JO 1 13 14 14 14 15 16 16 16 17 19 Double bond No. per molecule I 3 3 4 5 I 5 6 Stomach 1.1.7.1 5.48 1.51 1..6 6.6 6.9.66 1. 1.8 17.74 1.64.4 I.I I.9 19.3.75.9 1.51.6 1.34 1.83 3.3 TABLE. FATTY ACID COMPONENTS OF OILS CONTAINED IN VARIOUS BLUBBERS AND ORGANS OF BLACK RIGHT WHALE Liver.63.16 6. 1.39.81.1 6.69 4.8.48.9 1.1.93 1.34.36 1.9 1.8 1.83.94.73 1.65 16.64.85 1.86 3.67 Tongue.34.1.3 6.4 1.5.31.16 6.9 5.53.1.8 1.7.97 1.33.31 1.9 1.7 1.41.65.9 1. 17.98 1.5.1 4.35 Middle back.78.19 6.6.49.17.1 8.85 4.5 1.16.93 I 7.79 1.96 3.1 I.OJ.56 1.44.8.73 1.46 16.65 1.14 1.68.84 Thoracic Abdominal Brain Blubber Anterior of hind Umbilicus abdomipart of nal blow-hole Weight per cent of total fatty acids.4.35. 5.37 1..64.4 6.51 8.4 1.63 1.31 1.9.6 1.99 1.8.87.6 19.39.1.19.1 16.6 1. 3.3.54.6 5.76.68.65.35 6.6 5.15 1.1.81 1.14 1.6 1.3 I.3.65 1.81 3.39 I.73 1.3.5 15.56 1.17 1.3 4.16.66.53.14 6.61.76.51.9 8.37 7.4 1.45 1.36 1.6 17.61 1.64.43 1.39 1.5.3 1..57 1.46 17.66 1.6 1.78 4.9.33.15 5.4.38.45.19 5.95 3.6 1.13 1.3 1.81 1.55 1.16 1.61 1.15.31 1.15 1..1.47.6 3.79.81.6.3 5.83.8.46.33 6.5 4.57 1.91 1.6 1.19 17.96.1.44.97 1.6.97 1. 1.1.67 1.5 3.15 4.6.78.1.1 6.93 1.3 1.8.17 6.49 5.81.53 1.7 1.15.51 1.75..93 1.6.91 1..54 1.76 16.94 1.41 1.89 3.6 Blubber of fore part of genital aperture.37.17 8.II.7.34.13 6.96 5.3 1.3 1.4 1.54 19.56 1.41 1.99 1.17 1.63.9 1.34 1.5.1 15.17 1.91 1.6 3.88 Posterior back.8.8.1 6.1.4 1.6.11 5. 6.75 1.79 1.5 1.63.5 1.7.37 1.5 1.53.36 1.66 1.94.3 16.76.98 I.I I.3 -t""" -) -.J

168 TSUYUKI AND ITOH The each peak was quantitated by the method of Magidmann et al (196). All fatty acids were calculated as weight percentages of the total known fatty acids present. RESULTS AND DISCUSSION In this investigation, we confirmed about 5 kinds of fatty acids in the black right whale oil, as the results of the analysis are reported in Table. There are as saturated fatty acids, C 1, C 1, C 13, C 14, Cm C 16, C 17, C, C 19 and C, and as unsatturated fatty acids, C 14 monoenoic, C 14 dienoic, C 16 monoenoic, C 16 dienoic, C monoenoic, C dienoic, C trienoic, C monoenoic, C dienoic, C trienoic, C tetraenoic, C pentaenoic, C monoenoic, C pentaenoic and C hexaenoic. There is no remarkable difference in the fatty acid components of oils contained in various parts of the black right whale body. As the main component fatty acids belong to unsaturated fatty acids, these are C monoenoic.3-3.46% (average.7%), C monoenoic 17.74-.6% (av. 19.5%) and C pentaenoic 15.17-.67% (av. 17.1%). The next prominent fatty acids are C 16 saturated 5.- TABLE 3. EACH FATTY ACID CONTENT OF OILS IN VARIOUS BLUBBERS AND ORGANS (in order of high percentages) Fatty acid Double bond Order chain length No. per No. C atoms molecule Weight par cent of total fatty acids Average percentages 1.3-3.46.7 17.74-.6 19.5 3 5 15.17-.67 17.1 4 16 5.- 8.85 6.75 5 14 5.4-6.93 6. 6 16 3.6-8.4 5.57 7 6.3-4.9 3.65 8 3.3-3.1. 9 16 1.1-.66 1.77 1 4 1.-.5 1.75 II 5 1.3-.1 1.68 1.9-.56 1.65 13 1.16-.1 1.6 14 1.8-.93 1.51 15 3.19-.9 1.6 16.85-.6 1.3 17 19.65-1.9 1.16 17.8-1.1 19.1-1.73 1.1 14.38-1.5 1.6 1 14.17-1.8 1.5 1.33-1.1.61 3 1.1-1.1.8 4 15.9-.35. 5 13 -..5 Na., 197.

BLACK RIGHT WHALE OIL 169 TABLE 4. A COMPARISON OF SATURATED AND UNSATURATED FATTY ACID OF BLACK RIGHT WHALE OIL Fatty acid Weight per cent of total fatty acids chain length No. C atoms Saturated Averages Unsaturated Averages 1.33-1.1.61 1.1-.7..8 13 -..5 14 5.4-6.93 6..38-1.5 1.5 15.9-.35. 16 5.-8.85 6.75 4.6-1.9 7.34 17.8-1.1 1.8-.93 1.51 1.-7.9 3.5 19.65-1.9 1.16.9-.56 1.65 34.83-48.16 41.89 4.5-1.1 6.53 Total 19.55 79.86 8.85% (av. 6.75%), C 14 saturated 5.4-6.93% (av. 6.%) and C 16 monoenmc 3.6-8.4% (av. 5.57%). The total of the above mentioned fatty acids holds really 64.-88.93% (av. 75.61 %) of all total fatty acids. (Table 3) In comparison with saturated and unsaturated fatty acids, the proportions of total saturated fatty acids are 19.55% (average), and those of total unsaturated fatty acids are 79.86% (average) as shown in Table 4. In view of these facts, the principal fatty acids of the black right whale oil are monoenoic and polyenoic unsaturated fatty acids. SUMMARY 1. Fatty acid components of oils contained in 9 parts of s and 3 kinds of organs of black right whale, Eubalaena glacialis, caught in the Northern Pacific Ocean were analyzed by gas-liquid chromatograph using a hydrogen ionization detector on a DEGS column.. Fatty acid components of the above mentioned sample oils were as follows; C monoenoic C monoenoic C pentaenoic cl6 saturated C 14 saturated C 16 monoenoic C hexaenoic C trienoic C 16 dienoic C tetraenoic C pentaenoic C saturated.3-3.46% (av..7%) 17.74-.6% (av. 19.5%) 15.17-.67% (av. 17.1%) 5.- 8.85% (av. 6.75%) 5.4-6.93% (av. 6.%) 3.6-8.4% (av. 5.57%).3-4.9% (av. 3.65%).3-3.1% (av..%) 1.1-.66% (av. 1.77%) 1.-.5% (av. 1.75%) 1.3-.1 % (av. 1.68%).9-.56% (av. 1.65%) No., 197.

17 TSUYUKI AND ITOH c dienoic C saturated C trienoic C monoenoic C 19 saturated C 17 saturated C dienoic C 14 monoenoic C 14 dienoic C 1 saturated C 1 saturated C 15 saturated C 13 saturated 1.16-.1 % (av. 1.8-.93% (av..19-.9% (av..85-.6% (av..65-1.9% (av..8- % (av..1-1.73% (av..38-1.5% (av..17-1.8% (av..33-1.1 % (av..1-.7% (av..9-.35% (av. -.% (av. 1.6%) 1.51 %) 1.6%) 1.3%) 1.16%) 1.1%) 1.6%) 1.5%).63%).61 %).8%).%).5%) 3. A substantial part of the saturated acids were hexadecanoic (5.-8.85%) and tetradecanoic (5.4-6.93%). On the other hand, that of the unsaturated acids were nonadecamonoenoic (.3-3. 46 % ), octadecamonoenoic (17. 74-.6 %) and nonadecapentaenoic (15.17-.67%). 4. The difference in the fatty acid components of various s and organs of the black right whale was not found clearly. REFERENCES GAUGLITZ, E. J. Jr. and L. W. LEHMAN, 1963. The preparation of alkyl esters from highly unsaturated triglycerides. J. Am. Oil Chemists' Soc., 4: 197-198. MA.arnMANN, P., S. E. HERB, F. E. LUDDY and R. W. RIEMENSHNEIDER, 196. Fatty acid cow milk, II. Composition by gas-liquid chromatograph aided by other methods of fractionation. J. Am. Oil Chemists ' Soc., 39: 14-146. NEISON, G.J. and N. K. FREEMAN, 196. Phospholipide and phospholipide-fatty acid component of human serum lipo-protein fraction. J. Biol. Chem., 35: 578-583. TsUYUKI, H. and U. NARUSE, 1963. Studies on the oil of black right whale in the Northern Pacific Ocean. 17: 171-19. TsUYUKI, H. and U. NARUSE, 1964. Studies on the lipids in brain of black right whale in the Northern Pacific Ocean. : 173-. TsUYUKr, H., U. NARUSE, A. MocmzuKr and S. ITmr, 1964. Studies on liver oil of black right whale. Bull. Coll. Agr. & Vet. Med., Nikon Univ., : 17-4. No., 197.