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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 26 (1978), S. 1049-1050 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 27 (1979), S. 822-824 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 28 (1980), S. 578-579 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 28 (1980), S. 1169-1174 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 29 (1981), S. 1-4 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 21 (1973), S. 864-868 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 46 (1981), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Available lysine with its free ε-amino group can be chemically converted to homoarginine by means of a guanidination reaction using methylisourea (MIU). Various factors that can affect this reaction were investigated. For milk protein optimum conditions were found to be pH 10.8 for 96 hr at 20°C with a MIU concentration of 0.5M. Other protein sources had a different optimum pH for the guandination reaction. Addition of various carbohydrate sources and amounts did not interfere with the quantitation of available lysine.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food lipids 3 (1996), S. 0 
    ISSN: 1745-4522
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: ‘Alto’canola seed and sesame seed were toasted at 180, 200, 220, 240, and 260C, for 8 min or 10 min. As temperature increased, minor changes in fatty acid composition were observed. Darkness and blueness in canola oil increased with toasting temperatures up to 240C, and then decreased. The darkness, greenness and yellowness of sesame seed oil increased with increasing toasting temperature. The overall color of canola oil was significantly darker than that of sesame seed oil (α〈inlineGraphic alt="leqslant R: less-than-or-eq, slant" extraInfo="nonStandardEntity" href="urn:x-wiley:10657258:JFL1:les" location="les.gif"/〉 0.05). 2-Thiobarbituric acid (TBA) numbers for both oils increased as toasting temperature increased. TBA numbers of the canola oil increased with extended storage time up to 4 weeks and then decreased. For sesame seed oil, TBA numbers also were influenced by storage time, but less change was observed than for canola oil. 2-Thiobarbituric acid reactive substances (TBARS) content of canola oil was significantly higher than that for sesame seed oil when TBA numbers were compared to the same treatment.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food lipids 2 (1995), S. 0 
    ISSN: 1745-4522
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Headspace volatiles from ‘Alto’ canola oil toasted at 240C for 8 min were collected using TenaxR TA 60/80 (Supelco Inc., Bellefonte, PA). The TenaxR was washed three times with a total of 6 ml of solvent. The solvent extract was concentrated by drying in a hood at room temperature for 6 h. Two μl of concentrated extract were separated on a 30 m DB-1 capillary column (J & W Scientific, Folson, CA) with a Hewlett Packard (HP) 5890A gas chromatograph connected to a HP 5790 mass spectrometer. Volatiles were tentatively identified with a NBS 43 K.1 library by PBM (probability based on matching) search.Fifty seven peaks were detected by the mass spectrometer. Among those, 50 compounds were tentatively identified. 2-Furancarboxaldehyde, 5-methyl-2-furan carboxaldehyde, 5-(1-methyl ethyl)-1,3-cyclopentadiene, cyclododecane, undecanoic acid, tetradecanoic acid, 1-hexadecanol, hexadecanoic acid, 9-octadecenoic acid, octadecanoic acid, 2,5-dimethyl pyrazine, 3-ethyl-2,5-dimethyl pyrazine, [1,1′:3′,1″-terphenyl]-1′-ol and [1,1′:3′,1″-terphenyl]-4′-ol were the major volatile compounds.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food lipids 2 (1995), S. 0 
    ISSN: 1745-4522
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Sesame seed was toasted at 260C for 10 min. Oil was extracted with hexane at room temperature for 10 h. Post-treatment of the oil was not done. One half gram of TenaxR TA 60/80 (Supelco Inc., Bellefonte, PA) was used for trapping the volatile compounds from one hundred milliliters of toasted sesame seed oil. The procedure was continued for 24 h. The TenaxR TA was washed three times using polar and nonpolar solvents. The solvent extracts were combined and concentrated by drying in a hood at room temperature for 6 h. Two μl of concentrated extract were separated on a 30 m DB 1 bonded phase fused silica capillary column (J&W Scientific, Folsom, CA) with a Hewlett Packard (HP) 5890A gas chromatograph connected to a HP 5790 mass selective spectrometer. Volatiles were tentatively identified with a NBS 43K.1 library by PBM (probability based on matching) search.Seventy-nine peaks were detected by the mass selective detector. Among those, 66 peaks were tentatively identified. Dimethylsulfide, 4-methylthiazole, 2,4-dimethylthiazole, methylpyrazine, 2,5-dimethylpyrazine, dihydro-4,5-dimethyl-2(3H)-furanone, dodecane, tetradecane, 2,6-bis(1,1-dimethylethyl)-4-methyl phenol, N,N-bis (2-hydroxyethyl)-dodecamide, cyclododecane, 2,3-dihydro-1,1,3-trimethyl-3-phenyl-1H-indene, tetradecanoic acid, pentadecanoic acid, hexa-decenul, hexudecanoic acid, 9-octudecenoic mid, ocladecanoic acid, [1,1′:3′,1 ′I-tephenylJ-1′-ol and bis (2-ethyl hexy1)phthulate were the major volutiles identifled tentdively.
    Type of Medium: Electronic Resource
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