BT

Typical G.C. analysis

ferula cupularis leaf oil
Chemical composition and antibacterial activity of the essential oils from flower, leaf and stem of Ferula cupularis growing wild in Iran
#%LeftshiftComponents
1630.37  bicyclogermacrene
1536.55  bornyl angelate
1640.31delta- cadinene
1062.69  camphene
1002.90delta-2- carene
1600.17  caryophyllene oxide
1512.63  citronellyl butyrate
1082.37  decane
1305.02  dihydrolinalool acetate
1340.13trans-dimethoxycitral
1701.66beta- eudesmol
1571.87  eugenyl acetate
1610.11  geranyl butyrate
1680.21  guaiol
1155.78trans-isolimonene
1390.20para- menth-1-en-9-yl acetate
1134.05para- mentha-1,5,8-triene
9930.22beta- myrcene
1230.14  neral
1166.08allo- ocimene
1049.05beta- ocimene
1172.68neo-allo-ocimene
1361.65  octadecanal
1310.773- octen-1-yl acetate
2140.72  osthol
1092.36alpha- phellandrene
1104.18beta- phellandrene
10713.87beta- pinene
1220.62(Z)- sabinene hydrate acetate
1651.13  spathulenol
1203.45  terpinen-4-ol
1111.25alpha- terpinene
1463.70alpha- terpinyl isobutyrate
1190.363-thujenol
1411.39neo-iso- verbenyl acetate
Ziba Alipour, Poroshat Taheri, and Nasrin Samadi Department of Biology, Faculty of Science, Roudehen Islamic Azad University, Tehran, Iran, 2Department of Chemistry, School of Art & Science, Case Western Reserve University, Cleveland, OH, United State, and 3Department of Drug and Food Control, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran
ferula cupularis stem oil
Chemical composition and antibacterial activity of the essential oils from flower, leaf and stem of Ferula cupularis growing wild in Iran
#%LeftshiftComponents
1647.45  bornyl angelate
1501.421-endo- bourbonanol
1422.70beta- bourbonene
1203.03  camphor
1128.38delta-3- carene
1710.43  caryophyllene acetate
1582.57  citronellyl butyrate
1600.49  cuparene
1321.89(Z)-dihydro-alpha-terpinyl acetate
1690.62  dihydroeugenyl acetate
1781.75gamma- eudesmol acetate
1821.6614- hydroxy-alpha-humulene
1131.89  limonene oxide
1383.41  linalyl isobutyrate
1392.65para- menth-1-en-9-yl acetate
1182.39  myrcenone
1280.38(E)- ocimenone
2135.96  osthol
1161.57trans- pinene hydrate
1156.87(E)- sabinol
1332.19(E)- sabinyl acetate
1220.86alpha- terpineol
1371.23alpha- terpinyl acetate
1255.19  terpinyl acetate
1538.69alpha- terpinyl isobutyrate
1101.43cis-thujone
1300.523-thujul acetate
1140.30(Z)- verbenol
1475.20  verbenyl acetate
1462.18iso verbenyl acetate
1245.53para- cymen-9-ol
Ziba Alipour, Poroshat Taheri, and Nasrin Samadi Department of Biology, Faculty of Science, Roudehen Islamic Azad University, Tehran, Iran, 2Department of Chemistry, School of Art & Science, Case Western Reserve University, Cleveland, OH, United State, and 3Department of Drug and Food Control, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran
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