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DL-Camphor

Kampher-dl, . camphor oil (Pharm.) camphorated oil. -phoron, n. camphorphorone. -saure, /. camphoric acid, -sauresalz, n. camphorate. -spiritus, m. spirit of camphor, -wein, m. camphorated wine. [Pg.236]

Figure 14. Contour plot of the 360 MHz H-NMR correlation spectrum of dl-camphor. A 64 x256 data set was accumulated with quadrature phase detection in both dimensions and the data set was zero filled once in the dimension and symmetrized. T was 5 sec and t was incremented by 1.63 msec. Total accumulation time was 24 minutes and data workup and plotting took 15 min. Figure 14. Contour plot of the 360 MHz H-NMR correlation spectrum of dl-camphor. A 64 x256 data set was accumulated with quadrature phase detection in both dimensions and the data set was zero filled once in the dimension and symmetrized. T was 5 sec and t was incremented by 1.63 msec. Total accumulation time was 24 minutes and data workup and plotting took 15 min.
Synonyms AI3-18783 Alphanon 2-Bornanone DL-Bornan-2-one BRN 1907611 BRN 3196099 2-Camphanone DL-Camphor Camphor-natural Camphor-synthetic Caswell No. 155 EINECS 200-945-0 EINECS 207-355-2 EINECS 244-350-4 EPA pesticide chemical code 015602 Formosa camphor Gum camphor Iphanon Japan camphor 2-Keto-l,7,7-trimethyl-norcamphane Laurel camphor Matricaria camphor Norcamphor 2-Oxobornane Root bark oil Sarna Spirit of camphor Synthetic camphor l,7,7-Trimethylbicyclo[2.2.1]heptan-2-one 1,7,7-Trimethylnorcamphor UN 2717. [Pg.243]

C-07100,see2,4,5-T C-07101, see 2,4,5-Trichlorophenol C-07328, see Isoamyl alcohol C-07557, see TCDD C-08374, see Dodecane C-08380, see 2-Heptanone C-11043, see Methoxychlor C-11088, see 2,6-Dinitrotoluene C-11142, see Phenanthrene C-11160, see Thiram C-11233, see Dimethylphthalate C-14098, see 2-Methylnaphthalene C-10998, see 4-Aminobiphenyl C-11249, see Cyclohexane C-2292-52A, see Carbofuran CAF, see a-Chloroacetophenone Calmathion, see Malathion 2-Camphanone, see Camphor Camphechlor, see Toxaphene Camphochlor, see Toxaphene Camphoclor, see Toxaphene DL-Camphor, see Camphor Camphor-natural, see Camphor Camphor-synthetic, see Camphor Camphor tar, see Naphthalene Candaseptic, see p-Chloro-m-cresol Canogard, see Dichlorvos CAP, see a-Chloroacetophenone Caprolin, see Carbaryl... [Pg.1467]

K. Nakajima and T. Yasuda, Simultaneous determination of 1-menthol, dl-camphor and methyl salicylate in pharmaceutical preparations for external application using headspace gas chromatography, Chiba-Ken Eisei Kenkyusho Kenkyu Haboku, 5 14-18 (1984). [Pg.328]

The authors provided some experimental support for their hypothesis by performing various diastereoselective reactions on racemic or optically active compounds. Indeed, they found some differences in stereoselectivity between the two cases. Reduction of DL-camphor or D-camphor with lithium aluminum hydride, for example, gave ratios of isobomeol to bomeol of 7.93 and 9.20, respectively. [Pg.263]

DL-Camphor has been resolved by vapor-phase chromatography of the dia-stereolsomerlc ketals prepared with this readily available (by fermentation) diol. ... [Pg.774]

Figure 1. Diagrammatic representation of olfactory receptor cell activity during odour stimulation. The spot size is roughly proportional to spike frequency (spike/min). Receptor cells taken at random from the epithelium of a frog are identified hy a serial number in the left column (60 in all). ACE - acetophenone, ANI - anisole, BUT - n-butanol, CAM - DL-camphor, CDN - cyclodecanone, CIN - cineole, CYM, p-cymene, DCT D-citronellol, HEP - n-heptanol, ISO - isoamylacetate, IVA - isovaleric acid, LIM -D-linonene, MAC - methyl-amylketone, MEN - L-menthol, PHE - phenol, PHO -thiophenol, PYR - pyridine, THY - thymol, XOL - cyclohexanol, XON - cyclohexanone. (From Sicard Holley [7]). Figure 1. Diagrammatic representation of olfactory receptor cell activity during odour stimulation. The spot size is roughly proportional to spike frequency (spike/min). Receptor cells taken at random from the epithelium of a frog are identified hy a serial number in the left column (60 in all). ACE - acetophenone, ANI - anisole, BUT - n-butanol, CAM - DL-camphor, CDN - cyclodecanone, CIN - cineole, CYM, p-cymene, DCT D-citronellol, HEP - n-heptanol, ISO - isoamylacetate, IVA - isovaleric acid, LIM -D-linonene, MAC - methyl-amylketone, MEN - L-menthol, PHE - phenol, PHO -thiophenol, PYR - pyridine, THY - thymol, XOL - cyclohexanol, XON - cyclohexanone. (From Sicard Holley [7]).
More recent research investigates possibility of obtaining blends of PVC with conductive polymers. Figure 3.33 shows that concentration of conductive polymer is essential for conductivity. Optimal conductivity is obtained at a certain range of PVC concentration. The blends of poly(ethylene oxide), PEO, poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate), PEDOT-PSS, and PVC were designed to maximize thermal stability and conductivity. The thermal stability of the blend is increased by PEO and conductivity is increased by increasing concentration of PEDOT-ESS." Conductivity of PVC-NBR blends can be increased by addition of polyaniline-DL-camphor sulfonic acid, PANI-CSA. The conductivity of the blend increases linearly with the amount of PANI-CSA." ... [Pg.67]

See other pages where DL-Camphor is mentioned: [Pg.68]    [Pg.423]    [Pg.1622]    [Pg.134]    [Pg.149]    [Pg.150]    [Pg.51]    [Pg.391]    [Pg.110]    [Pg.386]    [Pg.395]    [Pg.390]    [Pg.371]    [Pg.360]   
See also in sourсe #XX -- [ Pg.81 ]



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