Use of a modified Abderhalden apparatus for comparing laboratory and industrial methods of isolating eastern redcedar essential oil

Forest Products Journal

Volumn 49, Issue 7, 1999, Pages 90-92

  Payne, Kirk W ^a,b   Wittwer, Robert ^a,b   Anderson, Steven ^a,b   Eisenbraun, Edmund J ^a,b  

^a OKLAHOMA STATE UNIVERSITY   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DISTILLATION; DRYERS (EQUIPMENT); GAS CHROMATOGRAPHY; SAWDUST; WOOD CHEMICALS;

ABDERHALDEN DRYING APPARATUS (ADA);

ESSENTIAL OILS;

ADA; JUNIPERUS VIRGINIANA;

EID: 0032595858     PISSN: 00157473     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Abraham, W.R., L. Ernst, B. Stumpf, and H.A. Arfmann. 1989. Microbial hydroxylations of bicyclic and tricyclic sesquiterpenes. J. Essent. Oil Res. 1(1):19-27.
2. Anonis, D.P. 1976. Perfumes in deodorants/antiperspirants. Drug and Cosm. Ind. 119:46-49,126-127.
3. Avramidis, S., R.L. Zwick, and J.B. Neilson. 1996. Commercial-scale RF/V drying of softwood lumber. Part 1. Basic kiln design considerations. Forest Prod. J. 46(5):44-51.
4. _ and _. 1996. Commercial-scale RF/V drying of softwood lumber. Part 2. Drying characteristics and lumber quality. Forest Prod. J. 46(6):27-36.
5. Bang, L. and G. Ourisson. 1975. Hydroxylation of cedrol by rabbits. Tetrahedron Lett. (24):1881-1884.
6. Black, P.J. 1991. No one's sniffing at aroma research now. Business Week (Industrial/Technology Ed.). 3245:82-83.
7. Chemical Marketing Report. 1998. 253(12):28.
8. Choney, J.H., M.W. Adkins, and E.J. Eisenbraun. 1987. A continuous ether/water extractor. J. Chem. Educ. 64:970.
9. Eisenbraun, E.J., H. Hall, and M.W. Adkins 1972. A laboratory steam generator and steam distillation apparatus. J. Chem. Educ. 49:441.
10. Gloess, W. 1989. Fragrance guide: Fragrances on the international market. No. 5. H&R Ed. Verlagsgesellschaft R. Gloess and Co. Hamburg, Germany. 228 pp.
11. Hanson, J.R. and H. Nasir. 1993. Biotransformation of the sesquiterpenoid, cedrol, by Cephalosporium aphidicola. Phytochemistry 33(4):835-837.
12. Hemmery, T.E. 1970. Economic uses of eastern red cedar. Economic Botany 24:39-41.
13. Kupchan, S.M., J.C. Hemingway, and J.R. Knox. 1965. Tumor inhibitors VII. podophyllotoxin, the active principle of Juniperus virginiana. J. Pharm. Sciences. 54(1): 659-660.
14. Lamare, V., J.D. Fourneron, R. Furstoss, C. Ehret, and B. Corbier. 1987. Microbial transformations. 9. biohydroxylation of alpha-cedrene and cedrol. Synthesis of an odoriferous minor component of cedar wood essential oil. Tetrahedron Lett. 28(50): 6269-6272.
15. Liu, F., S. Avramidis, and R.L. Zwick. 1994. Drying thick western hemlock in a laboratory radio-frequency/vacuum dryer with constant and variable electrode voltage. Forest Prod. J. 44(6):71-75.
16. Lykins, R.W. 1995. Estimation of above-ground eastern redcedar biomass, MSc thesis. Oklahoma State Univ., Stillwater, Okla. 74078 pp. 6-8, 33-46.
17. Maatooq, G., S. El-Sharkawy, M.S. Afifi, and J.P.N. Rosazza. 1993. Microbial transformation of cedrol. J. Nat. Prod. 56(7):1039-1050.
18. Mater Engineering LTD. 1993. Opportunities for rural development using eastern red cedar in southwestern Iowa. Mater Engineering LTD. Corvallis, Oreg.
19. Miyazawa, M., N. Hirokazu, and H. Kameoka. 1995. Biotransformation of (+)cedrol by plant patogenic fungus, Glomerella cingulata. Phytochemistry 40(1):69-72.
20. Payne, K.W. 1997. The recovery and analysis of steam volatile oils obtained from Juniperus virginiana L. MSc thesis. Oklahoma State Univ. Stillwater, Okla.
21. _, R. Wittwer, S. Anderson, and E.J. Eisenbraun. 1997. Use of a modified Abderhalden apparatus to determine moisture and oil content of eastern redcedar. Forest Prod. J. 48(7/8):91-93.
22. Tenaglia, A., E. Terranova, and B. Waegell. 1992. Ruthenium-catalyzed C-H bond activation. Oxyfunctionalization of nonactivated C-H bonds in the cedran series with RuO4 generated in situ. J. Org. Chem. 57(20): 5523-5528.
23. Teng, C.M., C.H. Lin, Y.H. Kuo, Y.L. Lin, and T.F. Huang. 1994. Antiplatelet and vasorelaxing actions of the acetoxy derivative of cedranediol isolated from Juniperus squamata. Planta Med. 60:209-213.
24. Trifilieff, E., L. Bang, and G. Ourisson. 1975. Hydroxylation of cedrol by dog. Tetrahedron Lett. (48):4307-4310.
25. United States Department of Commerce. 1998. Cleaning preparations and cosmetics. U.S. Industry & Trade Outlook '98. International Trade Administration, pp. 12,20,24.