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Borneol, bornyl acetate

Lane 3 With ascending hRf value borneol, bornyl acetate, guaiazulene... [Pg.283]

Cineole (40%-70 /o), thujone (about 5%), borneol, bornyl acetate, THC Diterpene carnosol... [Pg.158]

Benzylsalicylate DL-Borneol Bornyl acetate Bornyl formate Bornyl isovalerate Bornyl valerate Butan-3-one-2-yl butyrate Butter acids Butter esters n-Butyl acetate Butyl acetoacetate Butyl alcohol n-Butylamine Butyl anthranilate Butyl butyrate Butyl butyryl lactate a-Butylcinnamaldehyde Butyl cinnamate Butyl 2-decenoate Butyl ethyl malonate... [Pg.5288]

Benzyl acetate Benzyl propionate Bergamot (Citrus aurantium bergamia) oil y-Bisabolene Bitter almond (Prunus amygdalus amara) oil DL-Borneol Bornyl acetate L-Bornyl acetate Buchu leaves oil 3-Butylidenephthalide Butyl-(S)-lactate Butyl phenylacetate n-Butyl propionate 3-Cadinene 2-Carenyl methyl ketone... [Pg.5327]

Flowering aerial parts of E. purpurea contain less than 0.1% essential oil [14, 21, 67, 69, 74]. Bos et al. [96] showed that it contains borneol, bornyl acetate, pen-tadeca-8-en-2-one, germacrene D, caryophyllene, caryophyllene epoxide and palm-... [Pg.65]

Rosmarinus officinalis 1,8-Cineole, a-pinene, camphor, camphene, borneol, bornyl acetate... [Pg.625]

That the oil contains the following constituents, Z-a-pinene, d-a pinene, Z-limonene, Z-borneol, bornyl acetate and other esters of bomeol, Z-camphor, cineol, salicylic acid, aldehydes, formic, acetic, butyric ( ) and isovaleric acids, a non-volatile acid or lactone, and a blue constituent of high boiling-point. [Pg.295]

An oil distilled in Florida has been described, having an optical rotation of + 17 50, and containing much phellandrene. Miller s more recent work makes the authenticity of this sample doubtful. The oil contains traces of aldehydes and ketones, and, probably, of salicylic acid. The principal constituent of the oil is the dimethyl ether of thymo-hydroquinone. Phellandrene, borneol, bornyl acetate, linalol and sabinene ( ) are present in the oil. [Pg.298]

Bornyl Acetate.—The acetic acid ester is the most important of the series. It is a constituent of pine-needle and rosemary oils, and has a most fragrant and refreshing odour. It is prepared artificially by the action of acetic anhydride on borneol, in the presence of sodium acetate, or by the condensation of borneol with glacial acetic acid in the presence of a small amount of a mineral acid. It is absolutely necessary in the reproduction of any pine odour. It is a crystalline body, crystallising from peDroleum ether in rhombic hemihedric crystals melting at 29°. The optical activity depends on that of the borneol from which it has been prepared. It has the following characters —... [Pg.171]

Buchbauer G, Jager W, Jirovetz L, Meyer F, Dietrich H. (1992). [Effects of valerian root oil, borneol, isoborneol, bornyl acetate and isobornyl acetate on the motility of laboratory animals (mice) after inhalation]. Pharmazie. 1992 Aug. 47(8) 620-2. [Pg.494]

Kreis R Juchelka D, Motz C, Mosandl A, Chiral compounds in essential oils, DC Stereodifferentiation of borneol, iso-borneol and bornyl acetate, Dtsch Apoth Ztg, 131 198 1987, 1991. [Pg.183]

Bornyl acetate [5655-61-8] is a characteristic component of most conifer oils. It has a camphoraceous, pine-needle-like odor. Both (+)-bornyl acetate [20347-65-3] and (-)-bornyl acetate form colorless crystals the racemate [36386-52-4 ] is a colorless liquid. Bomyl acetate is prepared by esterification of borneol with acetic anhydride or via the process described under borneol (see p. 59). [Pg.72]

N.A. Alpha-thujone, fenchone, beta-thujone, sabinen, beyerene, bornyl acetate, camphor, borneol, sesquiterpenes, lignans, flavonoids.185-186 This herb is toxic. Against amoebas, parasites, bacteria, fungi, and viruses. [Pg.185]

Fig. 5-3. Examples of mono- and sesquiterpenes and their derivatives in softwood. 1, a-Pinene 2, /3-pinene 3, 3-carene 4, camphene 5, borneol (R = H), bornyl acetate (R = COCH3) 6, limonene 7, a-terpineol 8, dipentene 9, a-muurolene 10, 8-cadinene 11, a-cadinol 12, a-cedrene 13, longifolene 14, juniperol. Fig. 5-3. Examples of mono- and sesquiterpenes and their derivatives in softwood. 1, a-Pinene 2, /3-pinene 3, 3-carene 4, camphene 5, borneol (R = H), bornyl acetate (R = COCH3) 6, limonene 7, a-terpineol 8, dipentene 9, a-muurolene 10, 8-cadinene 11, a-cadinol 12, a-cedrene 13, longifolene 14, juniperol.
Borneol, (S3)66, 96 Bornyl Acetate, 460, 648 Z-Bornyl Acetate, 460 Bound Styrene, 782 Bovine Rennet, 133, (S3) 18 Brewer s Yeast, 440 Brilliant Blue FCF, 139, (S3)24 Bromelain, 132, 786, (S3)18 Bromide Identification Test, 753 Brominated Vegetable Oil, 48 Bromine, 0.1 N, 856 Bromine TS, 850 Bromine Water, 850 Bromocresol Blue, 860 Bromocresol Blue TS, 850... [Pg.119]

D-Bornyl acetate (= Borneol acetate) (monoterpene) Cardenolides (triterpene glycosides aglycones) see Table 4.1 for cardenolide Na+, K+-ATPase inhibitors Citral (= mixture of a-Citral (Geranial) (3-Citral (Neral) = trans-St av-3,7-Dimethyl-2,6-octadienal) (monoterpene) Citronellal (= 3,7-Dimethyloct-6-enal) (monoterpene) a-Farnesene (sesquiterpene)... [Pg.439]

Borneol acetate 10.4t, 10.5t Bornyl acetate 10.4t, 10.5t Boswellic acid 13.4Ht Bougainmlka RIP-I 9.1A Bouvardin 9.2a Bowringia lectin 12.2A Bradykinin 5.7B Bran 14.2o Brassica DEF PI 13.5J... [Pg.683]

Microbial oxidation of (-i-)-bornyl acetate (to 5-exo- and 5-endo-hydroxy-borneol) using Helminthosporium sativum is more efficient and regiospecific than that reported previously (Vol. 8, p. 51) with the enantiomer, in contrast to the conversion of (+)- and (-)-bornyl acetate, using Fusarium culmorum, into 5-exo-hydroxybornyl acetate. [Pg.66]

Pini silvestris aeth. Siberian spruce oil Abies sibirica LEDEB. 10% bornyl acetate, borneol 32%-44% bornyl acetate a-, p-pinene... [Pg.160]


See other pages where Borneol, bornyl acetate is mentioned: [Pg.295]    [Pg.163]    [Pg.401]    [Pg.92]    [Pg.208]    [Pg.231]    [Pg.188]    [Pg.852]    [Pg.853]    [Pg.201]    [Pg.201]    [Pg.552]    [Pg.285]    [Pg.295]    [Pg.163]    [Pg.401]    [Pg.92]    [Pg.208]    [Pg.231]    [Pg.188]    [Pg.852]    [Pg.853]    [Pg.201]    [Pg.201]    [Pg.552]    [Pg.285]    [Pg.145]    [Pg.215]    [Pg.134]    [Pg.1547]    [Pg.45]    [Pg.155]    [Pg.156]    [Pg.158]    [Pg.192]    [Pg.204]    [Pg.59]    [Pg.203]    [Pg.548]   
See also in sourсe #XX -- [ Pg.530 ]




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Borneol

Borneol acetate

Bornyl

Bornyl acetate

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