| Identification | Back Directory | [Name]
Bornyl acetate | [CAS]
76-49-3 | [Synonyms]
bornyl
FEMA 2159
bornyl aceate
Borneylacetate
BORNYL ACETATE
Bornylethanoate
Borneol,acetate
1-BORNYLACETATE
Borneol, acetate
dl-Bornylacetate
Bornylaceticester
endo-Bornylacetate
Bornyl acetic ether
2-Camphanol acetate
BORNYL ACETATE 97+%
Acetic acid isobornyl
acetic acid 2-bornyl ester
endo-2-Camphanyl ethanoate
Acetic acid isobornyl ester
1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol acetate
1,7,7-Trimethylbicyclo[2.2.1]heptane-2-yl=acetate
(1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) acetate
Bornyl acetate
Acetic acid isobornyl ester
endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acetate
Acetic acid 1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl
(1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) ethanoate
1,7,7-trimethyl-,acetate,endo-bicyclo[2.2.1]heptan-2-o
1,7,7-trimethyl-,acetate,endo-Bicyclo[2.2.1]heptan-2-ol
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-,acetate,endo-
Acetic acid 1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl ester
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, endo-
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, (1R,2S,4R)-
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-,acetate,(1R,2S,4R)-rel-
Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-, 2-acetate, (1R,2S,4R)-rel- | [EINECS(EC#)]
200-964-4 | [Molecular Formula]
C12H20O2 | [MDL Number]
MFCD00135944 | [MOL File]
76-49-3.mol | [Molecular Weight]
196.29 |
| Hazard Information | Back Directory | [Uses]
Antineoplastic; radioactive agent. | [Chemical Properties]
Bornyl acetate has a fresh, strong, piney odor and a fresh, burning taste. | [Chemical Properties]
Bornyl acetate occurs in its optically active forms and
as a racemate in many essential oils.
(1S,2R,4S)-(?)-Bornyl acetate is a characteristic component of
most conifer oils. It has a camphoraceous, pine-needle-like odor. Both (1R,2S,4R)-
(+)-bornyl acetate and (?)-bornyl acetate form colorless crystals;
the racemate is a colorless liquid. Bornyl acetate is prepared by
esterification of borneol with acetic anhydride or via the process described under
borneol.
Due to its characteristic pine-needle odor, bornyl acetate is frequently used in
conifer needle compositions, soaps, bath products, room sprays, and pharmaceutical
products. | [Occurrence]
Reported found in the oils of Abies canadensis, A. concolor, Picea canadensis, P. rubens, P. orientalis, Pinus
densiflora, Larix americana, Callitris drum-mondi, Abies alba, Pinus punulio, Abies sibirica L., and in coriander, thyme and valerian
oil; it has been identified in the essence from flowers of Chrysanthemum sincuse Sabin, in the distillate of Teucrium chamaedris
L., and in the fresh rhizomes of Valeriana officinalis L.; d-bornyl acetate is found in the essential oils of Callitris glauca, C. robusta,
C. gracilis, C. verrucosa and C. calcarata; the presence of acetate has been excluded from the essence of lavender and lavandin. | [Aroma threshold values]
Detection: 75 ppb to 1.38 ppm | [Taste threshold values]
Taste characteristics at 10 ppm: camphoreous, woody, mentholic, berry and seedy with soapy, woody
nuances. | [Synthesis]
l-Bornyl acetate occurs naturally in many oils distilled from the leaves of plants of the family Pinaceae; d-bornyl acetate is
found in the oils distilled from plants of the family Cupressaceae; bornyl acetate, therefore may be isolated by distillation and crystallization
from these; however, it is commonly prepared by direct acetylation of borneol; the first synthesis dates to 1889. | [storage]
Store at -20°C |
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