GC/MS BATCH NUMBER: CA0101

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GC/MS BATCH NUMBER: CA0101 ESSENTIAL OIL: CINNAMON CASSIA BOTANICAL NAME: CINNAMOMUM CASSIA ORIGIN: CHINA KEY CONSTITUENTS PRESENT IN THIS BATCH OF CINNAMON OIL % (E)-CINNAMALDEHYDE 79.1 (E)-O-METHOXYCINNAMALDEHYDE 8.8 (E)-CINNAMYL ACETATE 3.3 COUMARIN 2.0 BENZALDEHYDE 0.9 PHENYLETHYL ALCOHOL 0.5 (E)-O-METHOXYCINNAMYL ACETATE 0.5 (Z)-CINNAMALDEHYDE 0.4 SALICYLALDEHYDE 0.3 STYRENE 0.1 EUGENOL 0.04 LIMONENE 0.03 ACETOPHENONE 0.03 Comments from Robert Tisserand: This smells like a typical genuine Cassia oil, and it conforms to all 12 key constituents of the ISO standard. 510 2nd St S. Twin Falls, ID 83301 * 800-917-6577 * www.planttherapy.com Facebook.com/PlantTherapy * www.planttherapy.com/blog

Date : February 26, 2016 SAMPLE IDENTIFICATION Internal code : 16B22-PTH4-1-LC Customer identification : Cinnamon Cassia - China - CA010157R Type : Essential oil Source : Cinnamomum cassia Customer : Plant Therapy ANALYSIS Method : PC-PA-001-15E06, "Analysis of the composition of a liquid essential oil by GC-FID" (in French). Analyst : Alexis St-Gelais, M. Sc., chimiste Analysis date : 2016-02-26 Checked and approved by : Alexis St-Gelais, M. Sc., chimiste 2013-174 Note: This report may not be published, including online, without the written consent from Laboratoire PhytoChemia. This report is digitally signed, it is only considered valid if the digital signature is intact. Page 1 of 5

IDENTIFIED COMPOUNDS Identification Column: BP5 Column: WAX R.T. R.I. % % R.I. R.T. Molecular Class Hexanal 1.33 805 0.01 0.01 1028 1.30 Aliphatic aldehyde cis-hex-3-en-1-ol 1.97 861 tr 0.01 1342 5.08 Aliphatic alcohol Styrene 2.38 897 0.11 0.11 1197 3.03 Phenylpropanoid α-thujene 2.72 918 0.27 0.27 957 0.97 Monoterpene α-pinene 2.81 924 0.08 0.08 946 0.93 Monoterpene Camphene 3.07 940 0.04 0.04 1012 1.17 Monoterpene Sabinene 3.49 967 0.02 0.02 1067 1.62 Monoterpene β-pinene 3.53 970 0.02 0.02 1049 1.47 Monoterpene Benzaldehyde 3.61 974 0.89 0.91 1441 6.69 Simple phenolic Δ3-Carene 4.07* 1003 0.02 0.01 1100 1.88 Monoterpene α-phellandrene 4.07* 1003 [0.02] tr 1120 2.12 Monoterpene para-cymene 4.47* 1026 0.06 0.04 1213 3.25 Monoterpene Limonene 4.47* 1026 [0.06] 0.03 1144 2.41 Monoterpene 1,8-Cineole 4.52 1029 0.01 0.01 1151 2.49 Monoterp. ether Salicylaldehyde 5.03* 1058 0.27 0.29 1585 10.30 Simple phenolic γ-terpinene 5.03* 1058 [0.27] tr 1192 2.97 Monoterpene Benzyl alcohol 5.12 1063 0.04 0.05 1792 20.42 Simple phenolic Acetophenone 5.42 1080 0.03 0.11 1560 9.55* Simple phenolic Linalool 6.00 1109 0.01 0.02 1513 8.13 Monoterp. alcohol Phenylethyl alcohol 6.40 1127 0.54 0.58 1822 22.29 Simple phenolic 2-Methylbenzofuran 6.63 1138 0.03 Phenylpropanoid Camphor 6.73 1142 0.03 0.01 1423 6.37 Monoterp. ketone Hydrocinnamaldehyde 7.40 1173 0.54 Phenylpropanoid Borneol 7.52* 1178 0.19 0.08 1627 11.83 Monoterp. alcohol 3-Methylbenzofuran 7.52* 1178 [0.19] Phenylpropanoid α-terpineol 8.21 1204 0.02 0.05 1632 12.07 Monoterp. alcohol (Z)-Cinnamaldehyde 9.05 1227 0.41 0.34 1780 19.71 Phenylpropanoid Hydrocinnamyl alcohol 9.76 1246 0.02 0.03 1974 32.50 Phenylpropanoid o-anisaldehyde 9.82 1247 0.37 0.33 1840 23.59 Simple phenolic Phenylethyl acetate 10.23 1258 0.07 0.07 1727 16.62 Phenolic ester (E)-Cinnamaldehyde 12.20 1305 79.05 78.76 1930 29.71 Phenylpropanoid (E)-Cinnamyl alcohol 13.57 1329 0.16 0.27 2185 40.43 Phenylpropanoid α-terpinyl acetate 14.31 1342 0.02 0.01 1617 11.43 Monoterp. ester α-ylangene 14.53 1346 0.01 0.01 1418 6.26 Sesquiterpene α-copaene 14.93 1353 0.26 0.26 1430 6.51 Sesquiterpene Eugenol 15.32 1360 0.04 0.04 2072 36.99 Phenylpropanoid Unknown (m/z = 91, 121 (75), 108 (64), 164 (43)) 16.28* 1376 0.17 0.13 1994 33.65* Phenylpropanoid β-elemene 16.28* 1376 [0.17] 0.03 1527 8.55 Sesquiterpene β-caryophyllene 17.42 1396 0.10 0.08 1520 8.35 Sesquiterpene trans-α-bergamotene 18.86 1415 0.04 0.03 1529 8.62 Sesquiterpene Page 2 of 5

α-humulene 19.94 1429 0.01 0.02 1582 10.22 Sesquiterpene allo-aromadendrene 20.13 1432 0.04 [0.11] 1560 9.55* Sesquiterpene Coumarine 21.02 1443 2.04 2.13 2283 42.87 Coumarin (E)-Cinnamyl acetate 22.04* 1456 3.30 3.21 2051 36.20 Phenylpropanoid ester γ-muurolene 22.04* 1456 [3.30] 0.09 1611 11.17 Sesquiterpene Ethyl (E)-cinnamate 23.07 1470 0.04 0.09 2022 35.21* Phenylpropanoid ester α-muurolene 23.90 1481 0.04 0.04 1645 12.63 Sesquiterpene γ-cadinene 25.06 1495 0.06 0.04 1667 13.64 Sesquiterpene δ-cadinene 25.48 1500 0.12 0.09 1673 13.93 Sesquiterpene (E)-Cinnamic acid 25.91 1505 0.22 Phenylpropanoid trans-calamenene 26.31 1510 0.05 0.02 1734 16.99 Sesquiterpene trans-α-bisabolene 27.93 1529 0.02 0.03 1708 15.45 Sesquiterpene (E)-o- 29.49 1548 8.77 8.79 2315 43.62 Phenylpropanoid Methoxycinnamaldehyde Caryophyllene oxide 30.29 1558 0.08 0.06 1851 24.36 Sesquiterp. ether (E)-Nerolidol 30.88* 1565 0.19 [0.13] 1994 33.65* Sesquiterp. alcohol Spathulenol 30.88* 1565 [0.19] [0.09] 2022 35.21* Sesquiterp. alcohol (E)-o-Methoxycinnamyl 37.88 1688 0.45 0.41 2414 45.76 Phenylpropanoid ester acetate Benzyl benzoate 40.69 1767 0.05 0.05 2487 47.22 Phenolic ester Phenylethyl benzoate 43.28 1854 0.02 0.05 2572 48.87 Phenolic ester Total identified 99.28% 98.13% *: Two or more compounds are coeluting on this column [xx]: Duplicate percentage due to coelutions, not taken account in the identified total Note: no correction factor was applied OTHER DATA Physical aspect : Bright yellow liquid Refractive index : 1.6080 ± 0.0003 (20 C) CONCLUSION No adulterant, contaminant or diluent were detected using this method. Page 3 of 5

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