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2- ethyl heptanoate

Propionates and higher aliphatic esters generally become less toxic as the si2e of the alkyl carboxylate increases. As an example, the LD q (rat, oral) for ethyl nonanoate [123-29-5] is greater than 43 g/kg, and the LD q (rat, oral) for ethyl heptanoate [106-30-9] is 34.6 g/kg. [Pg.392]

Transesterification. The product obtained from cerate oxidation of the methoxyhydroperoxide from 1-octene in ethanol contained methyl heptanoate but no ethyl heptanoate, and the oxidation product of the ethoxyhydroperoxide in methanol contained ethyl heptanoate but no methyl heptanoate. [Pg.264]

A calibration standard was prepared by concentrating the solution containing 60 mg oil, 0.2 mg ethyl heptanoate and 160 ml pentane to the equivalent volume (ca. 0.2 ml). A Perkin - Elmer Sigma 2B gas chromatograph equipped with a flame ionization detector was used for analysis. The gas chromatographic conditions were as follows ... [Pg.90]

The encapsulated orange oil (0.1 g) was rehydrated in 7.5 ml distilled water via the use of a vortex mixer for 30 sec. Acetone (50 pi) containing 100 jug ethyl heptanoate (internal standard) was added and mixed for another 30 sec. This solution was forced through a preconditioned Sep-pak CIS reverse phase cartridge. [Pg.91]

The C8 aldehyde ester may be produced by cleavage of the 9-hydroperoxide of ethyl llnoleate followed by terminal hydroperoxidation. Further oxidation would produce the corresponding dicarboxylic acid which upon decarboxylation would give rise to ethyl heptanoate. The 8-alkoxy radical may also decompose to give the C7 alkyl radical, which would yield ethyl heptanoate or form a terminal hydroperoxide, and so on. Polymerization, both intra- and intermolecular, is also a major reaction in high temperature oxidation. Combination of alkyl, alkoxy, and peroxy radicals yields a variety of dimeric and polymeric compounds with C-O-C or C-O-O-C crosslinks. [Pg.97]

FID) response factors were not determined for each identified pineapple constituent. Qualitative and quantitative differences were noted between samples and it was observed (by GC/MS) that ethyl heptanoate eluted as a shoulder on the 6-methyl-5-hepten-2-one peak in some runs. Therefore, the use of 6-methyl-5-hepten-2-one was discontinued in later runs. The major compounds found were methyl hexanoate, methyl 2-methylbutanoate, methyl butanoate, methyl octanoate, methyl s-methylthiopropanaote and ethyl acetate. [Pg.228]

SYNS COGNAC OIL ENANTHYUC ETHER ETHYL ENANTHATE ETHYL HEPTANOATE ETHYL n-HEPTANOATE ETHYL HEPTOATE ETHYL HEPTYLATE ETHYL OENANTHATE ETHYL OENANTHYL.ATE FEMANo. 2437 OENANTHIC ETHER... [Pg.632]

Ethyl amyl ketone Ethyl butyrate Ethyl cinnamate Ethyl heptanoate Ethyl heptylate Ethyl lactate... [Pg.137]


See other pages where 2- ethyl heptanoate is mentioned: [Pg.440]    [Pg.74]    [Pg.218]    [Pg.52]    [Pg.142]    [Pg.1247]    [Pg.1334]    [Pg.259]    [Pg.106]    [Pg.21]    [Pg.272]    [Pg.89]    [Pg.244]    [Pg.1353]    [Pg.1353]    [Pg.554]    [Pg.555]    [Pg.639]    [Pg.706]    [Pg.706]    [Pg.112]    [Pg.632]    [Pg.632]    [Pg.1682]    [Pg.1682]    [Pg.52]    [Pg.155]    [Pg.358]    [Pg.487]    [Pg.573]    [Pg.622]    [Pg.737]    [Pg.701]    [Pg.151]    [Pg.153]    [Pg.452]   
See also in sourсe #XX -- [ Pg.440 ]

See also in sourсe #XX -- [ Pg.21 ]

See also in sourсe #XX -- [ Pg.554 ]

See also in sourсe #XX -- [ Pg.22 ]

See also in sourсe #XX -- [ Pg.133 ]

See also in sourсe #XX -- [ Pg.621 ]

See also in sourсe #XX -- [ Pg.235 ]




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Ethyl n-heptanoate

Heptanoic acid, 4-oxo-, ethyl ester

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