The type of uses and classifications may vary between different submissions to ECHA and for a full understanding it is recommended to consult the source data. J. volatile oil by supercritical carbon dioxide: influence of some process parameters, Flavour Fragr. Other identifiers . Methyl linoleate ≥98% (GC) Synonym: Linoleic acid methyl ester, Methyl cis,cis-9,12-octadecadienoate CAS Number 112-63-0. Structure of Conjugated Methyl Linoleate Hydroperoxide. ; Liang, Y.-Z. This site requires that Javascript be enabled. Food Chem., 54, 2006, 4780-4789. ass: Semi-standard non-polar; Column diameter: 0.25 mm; Column length: 30 m; Column type: Capillary; Heat rate: 4 K/min; Start T: 60 C; End T: 250 C; End time: 20 min; Start time: 2 min; CAS no: 112630; Active phase: HP-5MS; Carrier gas: He; Phase thickness: 0.25 um; Data type: Linear RI; Authors: Pino, J.A. Methyl linolelaidate. A fatty acid methyl ester of linoleic acid. Shop a large selection of Fatty Acyls products and learn more about Methyl Linoleate 95.0 %, TCI America. Res. View information & documentation regarding Methyl linoleate, including CAS, MSDS & more. 1 mL . ), Revista CENIC Ciencias Quimicas, 33(3), 2002, 115-119. ass: Standard non-polar; Column length: 25 m; Column type: Capillary; CAS no: 112630; Active phase: CP Sil 5 CB; Carrier gas: He; Data type: Normal alkane RI; Authors: Weyerstahl, P.; Marschall, H.; Weirauch, M.; Thefeld, K.; Surburg, H., Constituents of commercial Labdanum oil, Flavour Fragr. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 1959, 8 (10) , 1757-1763. 294.4756; All; Links to Resources; Names & Synonyms; Registry Numbers; Structure … The dehydro-dimer of methyl oleate was prepared and its structure determined as a model of a non-ring dimer for reference in studying the structure of other fatty dimer acids. Autoxidations were carried out on 5 g samples stirred at 80 C with oxygen in 5Q.ml Erlen meyer flasks. ; Molan, P.C., Extractives from New Zealand honeys. We will present our study on the effective computational modeling of bond dissociations in the FAMEs methyl linoleate and methyl oleate, which are the most common biodiesel products of soybeans and rapeseeds (also known as canola seeds). 112-63-0 . Methyl linoleate CAS # 112-63-0. J., 21, 2006, 906-911. ass: Semi-standard non-polar; Column diameter: 0.25 mm; Column length: 30 m; Column type: Capillary; Heat rate: 3 K/min; Start T: 60 C; End T: 240 C; CAS no: 112630; Active phase: DB-5; Carrier gas: He; Phase thickness: 0.25 um; Data type: Normal alkane RI; Authors: Tellez, M.R. METHYL LINOLEATE(112-63-0) 1 H NMR. SOME SPECIFIC FEATURES IN AUTOXIDATION OF METHYL LINOLEATE. m/z Click and drag to zoom, double click to reset zoom Hover over end of line for value. Your message has been sent. Methyl linoleate is a mixture with CNB89-S (*FEMA 3411*) is used as a flavouring ingredient Methyl linoleate belongs to the family of Lineolic Acids and Derivatives. Methyl octadeca-9,12-dienoate Res. Fatty acid methyl esters (FAME) are a type of fatty acid ester that are derived by transesterification of fats with methanol.The molecules in biodiesel are primarily FAME, usually obtained from vegetable oils by transesterification. Figures in parentheses after the mass number indicate the intensity of that peak relative to the strongest peak in the spectrum. Certified Reference Material. EC Number 203-993-0. 10.0 mg/mL in Heptane. Chromatogr., 12, 1989, 327-332. ass: Standard polar; Column diameter: 0.23 mm; Column length: 50 m; Column type: Capillary; Heat rate: 2 K/min; Start T: 80 C; End T: 200 C; CAS no: 112630; Active phase: Carbowax 20M; Data type: Kovats RI; Authors: Toda, H.; Mihara, S.; Umano, K.; Shibamoto, T., Photochemical studies on jasmin oil, J. Agric. ; Liang, Y.-Z. Methyl oleate produces small amounts of allylic keto-oleates (with CO on carbons 8-, 9-, 10- and 11), epoxy-stearate or epoxy-oleates (8,9-, 9,10- and 10,11-epoxy), dihydroxy-oleates (8,9-, 9,10-, and 10,11-diOH) and dihydroxystearates (between carbon-9 and carbon-11). The statement has been derived from substances/products of a similar structure or composition. ; Fraga, S.R.G., Chemical and aroma determination of the pulp and seeds of murici (Byrsonima crassifolia L.), J. Braz. Chromatogr., 220, 1981, 195-252. ass: Standard non-polar; Column diameter: 0.35 mm; Column length: 30 m; Column type: Capillary; Heat rate: 4 K/min; Start T: 60 C; End T: 270 C; Start time: 0.5 min; CAS no: 112630; Active phase: OV-101; Carrier gas: Hydrogen; Data type: Normal alkane RI; Authors: Ehrhardt, M.; Osterroht, C.; Petrick, G., Fatty-acid methyl esters dissolved in seawater and associated with suspended particulate material, Marine Chem., 10(1), 1980, 67-76. class: Semi-standard non-polar; Column diameter: 0.25 mm; Column length: 30 m; Column type: Capillary; Description: 50 0C (2 min) ^ 10 0C/min -> 150 0C ^ 15 0C/min -> 300 0C (10 min); CAS no: 112630; Active phase: 5 % Phenyl methyl siloxane; Carrier gas: Helium; Phase thickness: 0.25 um; Data type: Normal alkane RI; Authors: Huang, B.; Qin, L.; Chu, Q.; Zhang, Q.; Gao, L.; Zheng, H., Comparison of headspace SPME with hydrodistillation and SFE for analysis of the volatile components of the roots of Valeriana officinalis var. 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