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Ambrinol

In addition to large-scale process work, there is also some effort expended in providing synthetic methods for producing small amounts (<100 kg/yr) of materials needed for replacement of naturals that are being discontinued or in short supply. Examples are ambrinol (59) and dihydro-y-ionone (60) for the replacement of ambergris. More recendy, tincture of tonquin musk has been replaced by using, among other materials, mixtures of macrocyclic ketones and alcohols which have been found in the natural substance. [Pg.85]

Ambrettolic acid, physical properties, 5 35t a-Ambrinol, 24 575-576 Ambrocenide, 24 544 Amcymidol, 13 46... [Pg.44]

Ambergris Physeter macrocephalus (-)-Ambrox (95), (-)-a-ambrinol (96), (S)-dihydro-7-ionone (97) 112,114,115... [Pg.611]

Ambrinol (P25.2) can be produced by a simple acid-catalysed cyclisation of dihydro-y-ionone (P25.1) as shown in Figure S25 and so the latter is quite likely to be a precursor for the former in natural ambergris. [Pg.386]

See other pages where Ambrinol is mentioned: [Pg.39]    [Pg.316]    [Pg.84]    [Pg.36]    [Pg.80]    [Pg.174]    [Pg.454]    [Pg.85]    [Pg.550]    [Pg.85]    [Pg.184]    [Pg.550]    [Pg.233]    [Pg.36]    [Pg.37]    [Pg.37]    [Pg.142]    [Pg.59]    [Pg.150]    [Pg.353]    [Pg.356]    [Pg.356]    [Pg.357]    [Pg.357]    [Pg.550]   
See also in sourсe #XX -- [ Pg.80 ]

See also in sourсe #XX -- [ Pg.85 ]

See also in sourсe #XX -- [ Pg.156 , Pg.356 ]



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A-Ambrinol

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