GC/MS BATCH NUMBER: L40103

Similar documents
GC/MS BATCH NUMBER: LM0100

GC/MS BATCH NUMBER: L50109

GC/MS BATCH NUMBER: CF0108

GC/MS BATCH NUMBER: O50106

GC/MS BATCH NUMBER: CF0106

GC/MS BATCH NUMBER: TL0101

GC/MS BATCH NUMBER: R40106

GC/MS BATCH NUMBER: S30103

GC/MS BATCH NUMBER: TL0103

GC/MS BATCH NUMBER: BH0102

GC/MS BATCH NUMBER: E10106

GC/MS BATCH NUMBER: B50105

GC/MS BATCH NUMBER: EG0101

GC/MS BATCH NUMBER: LU0100

GC/MS BATCH NUMBER: P40105

GC/MS BATCH NUMBER: CLO105

GC/MS BATCH NUMBER: H20103

GC/MS BATCH NUMBER: P40106

GC/MS BATCH NUMBER: S40102

GC/MS BATCH NUMBER: CD0103

GC/MS BATCH NUMBER: Y50101

GC/MS BATCH NUMBER: CL0106

GC/MS BATCH NUMBER: CC0104

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: CE0104

GC/MS BATCH NUMBER: H90101

GC/MS BATCH NUMBER: CA0101

GC/MS BATCH NUMBER: F80104

GC/MS BATCH NUMBER: H20105

CERTIFICATE OF ANALYSIS - GC PROFILING

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: R10104

Alexis St-Gelais, M. Sc., chimiste

GC/MS BATCH NUMBER: G40105

SAMPLE IDENTIFICATION ANALYSIS. Date : December 1, 2016

GC/MS BATCH NUMBER: PJ0100

GC/MS BATCH NUMBER: SB5100

CERTIFICATE OF ANALYSIS - GC PROFILING

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: W10104

Customer: Hemp Traders Type: Oil Instrument: UPLC-PDA-MS Submitted: 06/20/17

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: TK0105

Alexis St-Gelais, M. Sc., chimiste

CERTIFICATE OF ANALYSIS - GC PROFILING

CERTIFICATE OF ANALYSIS - GC PROFILING

CERTIFICATE OF ANALYSIS - GC PROFILING

No adulterants, diluents, or contaminants were detected via this method. Conforms to 10/12 Iso Norms

GC/MS BATCH NUMBER: PJ0103

GC/MS BATCH NUMBER: PJ0102

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: F30105

CERTIFICATE OF ANALYSIS GC PROFILING

No adulterants, diluents, or contaminants were detected via this method. Conforms to ranges found in the literature. Extra caution should be taken

Essential Validation Services

Essential Validation Services

Essential Validation Services

Essential Validation Services

Essential Validation Services

No adulterants, diluents, or contaminants were detected via this method.

No adulterants, diluents, or contaminants were detected via this method.

No adulterants, diluents, or contaminants were detected via this method. Total Italidione level 4-5%.

Essential Validation Services

Natural Aroma Chemicals

Natural Aroma Chemicals

Natural Aroma Chemicals

Character Impact Odorants of Citrus Hallabong ([C. unshiu Marcov C. sinensis Osbeck] C. reticulata Blanco) Cold-pressed Peel Oil

Juniperus communis var. kelleyi, a new variety from North America

The Natural Choice for Flavor and Fragrance Ingredients. The Natural Choice for Flavor and Fragrance Ingredients. natural PRODUCT LIST

Extraction of Essential Oil from Citrus junos Peel using Supercritical Carbon Dioxide

The Natural Choice for Flavor and Fragrance Ingredients. The Natural Choice for Flavor and Fragrance Ingredients. natural PRODUCT LIST

Comparison of Peel Components of Sweet lime (Citrus limetta Risso) Obtained using Cold-press and Hydrodistillation Method

Comparison of leaf components of sweet orange and sour orange (Citrus sp.)

THE BREWING VALUE OF HOPS HOP & BREW SCHOOL A UG 29 S EPT 1, 2017, Y AKIMA

Influence of Rootstock on Essential Oil Composition of Mandarins

Little Things That Make A Big Difference: Yeast Selection. Yeast selection tasting

Chemical and Aroma Profiles of Yuzu (Citrus junos) Peel Oils of Different Cultivars

Safety Assessment of Citrus Flower- and Leaf-Derived Ingredients as Used in Cosmetics

Composition of the essential oils of Pinus nigra Arnold from Turkey

CHEMOSYTEMATICS OF JUNIPERUS: EFFECTS OF LEAF DRYING ON ESSENTIAL OIL COMPOSITION III

Hops. Philippe Lefèvre Yakima Chief

The effects of rootstock on the flower components of Clementine Mandarin (Citrus clementina)

Comparison of volatile oils of Juniperus coahuilensis in fresh seed cones vs. cones in fresh gray fox scat

CHEMOSYTEMATICS OF JUNIPERUS: EFFECTS OF LEAF DRYING ON ESSENTIAL OIL COMPOSITION II ABSTRACT

FOOD QUALITY CONTROL USING PEPTIDE BASED GAS SENSOR ARRAYS

Understanding the impact hopping rate has on the aroma quality and intensity of beer dry hopped with Cascade

Re-examination of the volatile leaf oils of Juniperus flaccida, J. martinezii, and J. poblana

Brittany M. Xu, George L. Baker, Paul J. Sarnoski, and Renée M. Goodrich-Schneider

Effects of Crop Season and Maturity Stage on the Yield and Composition of Essential Oil of Coriander (Coriandrum sativum L.) Fruit

Life Science and Chemical Analysis Solutions. Key Words: GCxGC-TOFMS, SPME, Food and Flavors. LECO Corporation; Saint Joseph, Michigan USA

Volatile constituents of cultivated Origanum vulgare L. inflorescences and leaves

Leaf Volatile Compounds of Seven Citrus Somatic Tetraploid Hybrids Sharing Willow Leaf Mandarin (Citrus deliciosa Ten.) as Their Common Parent

THE BIODIVERSITY OF Lavandula angustifolia MILL. F 1 HYBRIDS

Global Cardamom Oil Market - Trends & Forecast,

by trained human panelist. Details for each signal are given in Table 2.

Fermentation-derived aroma compounds and grape-derived monoterpenes

Agilent J&W DB-624 Ultra Inert Capillary Column Screens Distilled Spirits by GC/MS Static Headspace

Research Article Chemical Composition of Essential Oil from the Peel of Chinese Torreya grandis Fort

Alphonso is the most popular and most exported mango [Mangifera indica L.

Characterization of Volatile Organic Compounds from Peel of Citrus medica L. by Headspace Trap (HS-Trap)Sampling TechniqueCoupled with GCMS.

Transcription:

GC/MS BATCH NUMBER: L40103 ESSENTIAL OIL: LAVENDER BOTANICAL NAME: LAVANDULA ANGUSTIFOLIA ORIGIN: BULGARIA KEY CONSTITUENTS PRESENT IN THIS BATCH OF LAVENDER OIL % LINALOOL 36.6 LINALYL ACETATE 28.3 Trans-β-FARNESENE 4.1 β-caryophyllene 3.5 LAVANDULYL ACETATE 3.0 Cis-β-OCIMENE 2.9 TERPINEN-4-OL 2.7 3-OCTANONE 2.6 Trans-β-OCIMENE 2.6 α-terpineol 1.2 LAVANDULOL 1.1 Comments from Robert Tisserand: A delightful Bulgarian lavender oil. The linalool is slightly high, and the linalyl acetate slightly low compared to the ISO standard for Bulgarian lavender oil, but it is a genuine oil with no sign of adulteration. 510 2nd St S. Twin Falls, ID 83301 * 800-917-6577 * planttherapy.com facebook.com/planttherapy * essentialoilblogging.com

Date : September 18, 2015 SAMPLE IDENTIFICATION Internal code : 15I11-PTH5-1-HM Customer identification : Lavender - Bulgaria - L4010357 Type : Essential Oil Source : Lavandula angustifolia Customer : 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. Analysis date : 2015-09-11 Page 1 of 5

IDENTIFIED COMPOUNDS Identification Colonne: BP5 Colonne: WAX R.T. R.I. % % R.I. R.T. Molecular Class Ethanol 0.28 477 tr tr 897 0.66 Aliphatic alcohol Acetone 0.30 484 0.02 0.02 717 0.41 Aliphatic ketone 2-Methyl-3-buten-2-ol 0.42 532 0.01 0.01 1010 1.22* Aliphatic alcohol Isovaleral 0.54 576 0.01 0.01 841 0.55* Aliphatic aldehyde 2-Methylbutyral 0.55 581 0.02 [0.01] 841 0.55* Aliphatic aldehyde Hexan-2-ol? 1.44 816 0.04 Aliphatic alcohol Methyl hexyl ether 1.50 821 0.18 0.18 913 0.73 Aliphatic ether Hexanol 2.18 881 0.13 0.14 1322 5.05 Aliphatic alcohol Tricyclene 2.62 914 0.02 0.02 963 0.96 Monoterpene α-thujene 2.72 920 0.08 0.08 995 1.11 Monoterpene α-pinene 2.80 926 0.13 0.13 984 1.06 Monoterpene Camphene 3.06* 942 0.12 0.12 1024 1.34 Monoterpene α-fenchene 3.06* 942 [0.12] [0.01] 1010 1.22* Monoterpene Sabinene 3.48 969 0.03 0.04 1082 1.86 Monoterpene β-pinene 3.52 971 0.03 0.03 1063 1.69 Monoterpene Myrcene 3.83 991 0.70 0.70 1135 2.45 Monoterpene Octan-3-one 3.88 994 2.61 2.29 1220 3.55 Aliphatic ketone Octen-3-ol 4.03 1004 0.14 0.13 1424 6.72* Aliphatic alcohol Δ3-Carene 4.06* 1005 0.10 0.07 1110 2.15 Monoterpene α-phellandrene 4.06* 1005 [0.10] 0.03 1125 2.34 Monoterpene Octan-3-ol 4.14 1010 0.42 0.46 1367 5.73 Aliphatic alcohol α-terpinene 4.25 1016 0.04 0.05 1139 2.51 Monoterpene Hexyl acetate 4.34 1021 0.89 0.87 1243 3.89 Aliphatic ester Limonene 4.46* 1028 0.46 0.36 1157 2.73 Monoterpene para-cymene 4.46* 1028 [0.46] 0.15 1228 3.68 Monoterpene β-phellandrene 4.49 1029 0.26 0.97 1163 2.80* Monoterpene 1,8-Cineole 4.51 1031 0.73 [0.97] 1163 2.80* Monoterp. ether cis-β-ocimene 4.68 1040 2.93 3.05 1207 3.38* Monoterpene trans-β-ocimene 4.85 1050 2.56 2.53 1222 3.59 Monoterpene γ-terpinene 5.00 1059 0.14 [3.05] 1207 3.38* Monoterpene cis-linalool oxide (fur.) 5.28 1075 0.10 0.15 1401 6.24 Monoterp. alcohol Terpinolene 5.45 1084 0.10 0.09 1240 3.85 Monoterpene trans-linalool oxide (fur.) 5.58 1092 0.08 [0.13] 1424 6.72* Monoterp. alcohol Linalool 6.07* 1116 36.96 36.64 1522 9.01 Monoterp. alcohol Octen-3-yl acetate 6.07* 1116 [36.96] 0.88 1353 5.51 Aliphatic ester Octan-3-yl acetate 6.22 1123 0.23 0.25 1311 4.88 Aliphatic ester Camphor 6.72 1146 0.26 0.23 1442 7.08 Monoterp. ketone Lavandulol 7.24 1170 1.09 1.19 1634 13.18 Monoterp. alcohol Borneol 7.42 1177 0.47 0.47 1637 13.32 Monoterp. alcohol Terpinen-4-ol 7.58 1185 2.69 2.66 1548 9.87 Monoterp. alcohol Cryptone 7.82 1196 0.18 0.22 1586 11.11 Monoterp. ketone Page 2 of 5

Hexyl butyrate 7.89 1199 0.57 0.44 1386 6.02 Aliphatic ester α-terpineol 8.10 1205 1.22 1.18 1642 13.56 Monoterp. alcohol γ-terpineol 8.38 1213 0.01 0.02 1649 13.87 Monoterp. alcohol Nerol 9.04 1231 0.17 0.21 1750 19.38 Monoterp. alcohol Neral 9.59 1245 0.07 0.04 1619 12.48 Monoterp. aldehyde Linalyl acetate 9.90 1254 28.25 28.32 1528 9.20 Monoterp. ester Geraniol 10.08 1259 0.48 0.52 1804 22.79 Monoterp. alcohol Geranial 10.70 1275 0.02 0.03 1669 14.84 Monoterp. aldehyde Lavandulyl acetate 11.24 1290 3.02 2.97 1572 10.64 Monoterp. ester Neryl acetate 15.13 1362 0.38 0.43 1680 15.36 Monoterp. ester β-elemene 15.91 1375 0.09 0.10 1538 9.52* Sesquiterpene Geranyl acetate 16.45 1385 0.60 0.59 1711 17.02 Monoterp. ester Hexyl hexanoate 16.80 1391 0.11 0.12 1597 11.46* Aliphatic ester β-caryophyllene 17.34 1400 3.48 3.42 1536 9.46 Sesquiterpene Aromadendrene 18.73 1419 0.09 [0.10] 1538 9.52* Sesquiterpene α-humulene 19.74 1432 0.07 [0.12] 1597 11.46* Sesquiterpene trans-β-farnesene 21.07 1449 4.14 4.57 1631 13.04* Sesquiterpene Germacrene D 21.79 1459 0.53 [4.57] 1631 13.04* Sesquiterpene Caryophyllene oxide 29.89 1559 0.17 0.16 1858 26.74 Sesquiterp. ether Total identified 98.43% 98.34% *: 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 : Clear liquid Refractive index : 1.4590 ± 0.0003 (20 C) CONCLUSION No adulterant, contaminant or diluent were detected using this method. 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 3 of 5

Page 4 of 5

Page 5 of 5