Benzyl Isovalerate

Apple Allyl butyrate, cyclohexylvalerate, isovalerate, propionate Benzyl isovalerate Butyl isovaleratc. valerate Cinnamyl formate, isobuiyrate. isovaleraie Citronellyl isovaleraie Cyclohexyl acetate, butyrate, isovalerate Ethyl isovalerate, valerate Isopropyl acetate, valerate 2-Methylallyl butyrate Methyl butyrate Terpenyl isovaleraie... [Pg.648]

Benzyl Isovalerate 192.26/Ci2Hi602/ colorless liq/ s—ale, most fixed 1 mL in 3... [Pg.528]

Benzoylbenzene, 458 Benzoyl Peroxide, 43 Benzyl Acetate, 458, 570, 608 Benzyl Alcohol, 458, 570, 646 Benzyl Benzoate, 458, 647 Benzyl Butyrate, 458, 647 Benzyl n-Butyrate, 458 Benzyl Cinnamate, 458, 647 Benzyl Formate, 460, 608 Benzyl Isobutyrate, 460, 608 Benzyl Isovalerate, 460, 648, (Sl)60 Benzyl 3-Methyl Butyrate, 460 Benzyl 2-Methyl Propionate, 460 Benzyl Phenylacetate, 460, 608 Benzyl Propanoate, 460 Benzyl Propionate, 648 Benzyl Salicylate, 460, 682 Bergamot Oil, Coldpressed, 44, 575 beta Cyclodextrin, (Sl)15 Beta-1,3-Glucan, (S3)15 BHA, 44 BHT, 45... [Pg.119]

SYNS BENZYL ISOVALERATE (FCC) BENZYL-3-METHYLBUTANOATE BENZYL-3-METHYL BUTYRATE FEMA No. 2152 ISOPENTANOIC ACID, PHENYLMETHYL ESTER ISOPROPYL ACETIC ACID, BENZYL ESTER 3-METHYLBUTANOIC ACID, PHENYLETHYL ESTER... [Pg.807]

F.43) Butanoic acid, 3-methyl-, phenylmethyl ester, benzyl 3-methylbutanoate, benzyl isovalerate [103-38-8 FEMA 2152... [Pg.179]

A Benzyl isovalerate 25A Isobutyl butyrate 42A Pent-4-en-4-oUde... [Pg.1059]

Isopentane thiol. See 3-Methyl-1-butanethiol Isopentanoic acid. See Isovaleric acid Isopentanoic acid, phenylmethyl ester. See Benzyl isovalerate Isopentanol. See Isoamyl alcohol lsopent-2-enyl acetate. See Prenyl acetate Isopentyl acetate. See Isoamyl acetate Isopentyl alcohol. See Isoamyl alcohol s-lsopentyl alcohol. See 3-Methyl-2-butanol Isopentyl alcohol acetate. See Isoamyl acetate Isopentyl alcohol, cinnamate. See Isoamyl cinnamate... [Pg.2241]

Isopropylacetic acid. See Isovaleric acid Isopropyl acetic acid, benzyl ester. See Benzyl isovalerate... [Pg.2247]

Benzyl butyl ether Benzyl butyrate Benzyl cinnamate Benzyl 2,3-dimethylcrotonate Benzyl dipropyl ketone Benzyl disulfide Benzyl ether Benzyl ethyl ether Benzyl formate Benzylidene acetone Benzyl isobutyrate Benzyl isovalerate Benzyl mercaptan Benzyl methoxyethyl acetal Benzyl phenylacetate Benzyl propionate Benzylsalicylate Birch (Betula pendula) tar oil DL-Bomeol Bomyl acetate... [Pg.5282]

Benzyl isovalerate Benzyl mercaptan Benzyl methoxyethyl acetal Benzyl phenylacetate Benzyl propionate... [Pg.5288]

Amyl phenylacetate Amyl valerate Amyris (Amyris balsamifera) oil trans-Anethole Anisaldehyde diethyl acetal Anise (Pimpinella anisum) extract p-Anisonitrile Anisyl alcohol o-Anisyl alcohol p-Anisyl isobutyrate Bay (Pimenta acris) oil Benzaldehyde propylene glycol acetal Benzothiazole Benzylacetone 2-Benzylheptanol Benzyl isoamyl ether Benzyl isovalerate Benzyl methyl ether Benzyl octanoate ... [Pg.5320]

Methyl 3-phenylpropionate 203-093-8 Methyl cinnamate 203-095-9 Benzyl isobutyrate 203-096-4 Di benzyl 203-098-5 Eccobrite RB Eccobrite RB-6 Stilbene trans-Stilbene Tinopal UNPA-GX 203-104-6 Ethyl cinnamate 203-105-1 Benzyl butyrate 203-106-7 Benzyl isovalerate 203-109-3 Benzyl cinnamate 203-113-5... [Pg.6725]

Amyl benzoate Benzyl isovalerate Benzyl-2-methyl butyrate Benzyl valerate Butyl phenylacetate p-Cresyl isovalerate Cuminyl acetate Dimethyl benzyl carbinyl acetate Ethyl-4-phenylbutyrate Greeny I acetate Isoamyl benzoate Isobutyl phenylacetate Isoeugenyl ethyl ether a-Methylbenzyl butyrate Phenethyl butyrate Phenethyl isobutyrate... [Pg.7078]

Mixed Tischtchenko reactions were also studied by Nord. In these reactions he isolated benzyl isovalerate and isoamyl benzoate from benzaldehyde and isovaleralde-hyde as well as benzyl acetate, ethyl acetate, and benzyl benzoate from benzaldehyde and acetaldehyde. Orloff also reported the synthesis of benzyl isobutyrate and isobutyl benzoate from benzaldehyde and isobutyraldehyde. However, the mechanism of mixed Tischtchenko reactions is rather complex. For example, in the reaction of benzaldehyde and -butyraldehyde, either of the carbonyl groups may coordinate with the aluminium alkoxide. In fact the carbonium ion formed in butyraldehyde is more active than that in benzaldehyde and further reaction may proceed with the carbonium ion of the former type. The overall mechanism may be explained by the following equations (2.331)-(2.334) ... [Pg.143]

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