ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

Similar documents
ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

ENREGISTREMENT DES BULLETINS ANALYTIQUES : CHROMATOGRAPHIE ESSENTIAL OIL CHROMATOGRAPHY SHEET RECORDS

GC/MS BATCH NUMBER: H20106

GC/MS BATCH NUMBER: N10101

Customer : Comments and Conclusions : Daniel Dantin - Laboratory director

GC/MS BATCH NUMBER: G30103

SAMPLE IDENTIFICATION ANALYSIS. Date : January 19, 2017

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: L70106

GC/MS BATCH NUMBER: G40106

GC/MS BATCH NUMBER: P50102

GC/MS BATCH NUMBER: C90110

GC/MS BATCH NUMBER: O10106

GC/MS BATCH NUMBER: F00100

GC/MS BATCH NUMBER: C80101

GC/MS BATCH NUMBER: C90106

GC/MS BATCH NUMBER: BG0100

CERTIFICATE OF ANALYSIS - GC PROFILING

GC/MS BATCH NUMBER: F90100

GC/MS BATCH NUMBER: G50106

Presence of Compounds in Ubos (Spondias mombin)

Certificate of Analysis / Certificat d analyse

Phytochemical and Biosynthetic Studies of Lignans, with a Focus on Indonesian Medicinal Plants Elfahmi, [No Value]

GC/MS BATCH NUMBER: J10105

GC/MS BATCH NUMBER: C50101

Customer: Stud Horse Mountain Extracts Type: Concentrate Instrument: HPLC-PDA Submitted: 09/22/17

AROMA CHEMICAL PRODUCT LIST

GC/MS BATCH NUMBER: F50101

ISSN: CHANGE IN ANTIOXIDANT ACTIVITY OF SPICES TURMERIC AND GINGER ON HEAT TREATMENT

Presence of Compounds in Boldo (Peumus boldus)

Analytical Results SC Laboratories Oregon LLC ORELAP# 4133/OLCC# D SW 74th Ave Suite 110, Tigard, OR

ICC Iranian Chemical Communication

Determining Terpene Profiles of Cannabis Strains Using GC and GCxGC with High Performance TOFMS

*Shaheed Rajguru College of Applied Sciences, Department of Food Technology, University of Delhi

GC/MS BATCH NUMBER: J10101

Simplified Cannabis Terpene Profiling by GCMS

GC/MS BATCH NUMBER: R30102

ABTRACT. Key words: solvent extraction, XAD-2 resin, free and glycosidically bound volatile compound, kaffir lime leaves

Antique lavender essential oil from 1945, its chemical composition and enantiomeric distribution

GC/MS BATCH NUMBER: J10102

12025 NE Marx St. Portland, OR Green Leaf Lab proudly follows / ISO/IEC 17025:2005(E) Quality Standards

GC/MS BATCH NUMBER: J10104

Scholars Research Library. Annals of Biological Research, 2012, 3 (2): (

Headspace Analysis of Volatile Compounds Coupled to Chemometrics in Leaves from the Magnoliaceae Family

LEMONGRASS ESSENTIAL OIL SPECIFICATION PRODUCT IDENTIFICATION: Product Name: LEMONGRASS OIL Botanical Name: Cymbopogon flexuosus Cymbopogon flexuosus

SUPPLEMENTARY MATERIAL Chemical composition, cytotoxicity, antimicrobial and antifungal activity of several essential oils

Analytical Results SC Laboratories Oregon LLC ORELAP# 4133/OLCC# D SW 74th Ave Suite 110, Tigard, OR

Aromas From Quebec. II. Composition of the Essential Oil of the Rhizomes and Roots of Asarum canadense L.

Chemical Composition of Curcuma Longa Leaves and Rhizome Oil from the Plains of Northern India

International Archive of Applied Sciences and Technology, Vol 1 [2] December 2010: 32-36

Presentation 7 Feb 2, 2019

Ali M et al. IRJP 2011, 2 (9), INTERNATIONAL RESEARCH JOURNAL OF PHARMACY ISSN Available online

Ingredient Specialities

The Effect of Geographical Location on Sour orange (Citrus aurantium L.) Flower Components

Composition and variability of the essential oils of the leaves and berries from Juniperus navicularis

Volatile Compounds from the Different Organs of Houttuynia cordata and Litsea cubeba (L. citriodora)

Flavor and Fragrance Materials of Natural Origin

Analytical Results SC Laboratories Oregon LLC ORELAP# 4133/OLCC# D SW 74th Ave Suite 110, Tigard, OR

Essential oil composition and variability of Thymus lotocephalus and Thymus mourae

Charles S. McEnally* and Lisa D. Pfefferle. Department of Chemical Engineering and Center for Combustion Studies, Yale University, New Haven

Robert P. Adams* Biology Department, Baylor University, Box 727, Gruver, TX, 79040, USA

Comparative Study on Volatile Compounds of Alpinia japonica and Elettaria cardamomum

Agilent GC-MS: Headspace-GC-MS systems for the analysis of Residual Solvents and Terpenes

SUPPLEMENTARY MATERIAL

Akungba- Akoko, Nigeria 2 Department of Chemistry, Nasarawa State University, Keffi. Nigeria

Essential oil of geranium (Pelargonium ssp.)

KASHRUTH CERTIFICATION This is to certify that the following products, produced by:

Cannabis Reference Standards

State of knowledge on abiotic hapten formation (hydrolysis) using examples of fragrance ingredients and state of the art on the technical management

GC-FID and GC/MS analyses and Antimicrobial activity of Croton greveanus, C. borarium and C. geayi (Euphorbiaceae) essential oils from Madagascar

Effect of Harvesting Treatments and Distillation Methods on the Essential Oil of Lemon Balm and Apple Geranium Plants

Chemical variability of peel and leaf essential oils of 15 species of mandarins

SECTION 4 PITTOSPORACEAE ANALYSIS OF THE VOLATILE COMPONENTS IN P. DASYCAULON AND P. NAPAULENSE

J. Life Sci. Biomed. 4(4): , , Scienceline Publication ISSN

FirstReportingontheChemistryandBiologicalActivityofaNovelBoswelliachemotypeTheMethoxyAlkaneFrankincense

Supplement of Evaluation of NO + reagent ion chemistry for online measurements of atmospheric volatile organic compounds

We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists. International authors and editors

Cuminum cyminum L. and Carum carvi L. seeds from Iran

Essential Oil Composition from Juniperus communis Originated from Albania

AppNote 9/2000. Flavor Profi ling of Different Olive Oils with Rancidity-Monitoring by Thermal Extraction GC/MS KEY WORDS ABSTRACT

PRODUCT NAME PRODUCT CODE FEMA

Certi cate of Analysis

Optimization of the extraction of bioactive compounds from Helichrysum plicatum DC and formulation of phytopoduct with biological activity

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Composition of the essential oil and the hydrosol of the roots of Ligusticum porteri

Certi cate of Analysis

Certi cate of Analysis

Certi cate of Analysis

Transcription:

FORM-LAB005-B Page 1 sur 9 Date : 06/08/2012 Référence produit / Product reference : FLE043 Huile essentielle de / Essential oil of : Helichryse sauvage / Helichrysum Italian Numéro de lot / Lot Number : F120712F Densité à 20 C (g/cm 3 ) / Density to 20 C (g/cm 3 ) : [0.880 0.920] Indice de réfraction / Refractive index : [1.460 1.475] Pouvoir rotatoire à 20 C / Optical rotation to 20 C : [-20 ; +10 ] Mode de culture / Culture mode : Sauvage / Wild Pays / Country : France (Corse) Date de production / Production date : 2012 D.L.U. / Shelf life : 07/2017 Mode d extraction / Extraction mode : Distillation à la vapeur / Steam distillation % Bio / % Organic : 100% Bio / 100% Organic Nom Latin / Latin Name : Helichrysum italicum Parties utilisées / Used Parts : Sommités Fleuries / Flowering Top Hydocarbures monoterpéniques alcools monoterpéniques cétones monoterpéniques aldéhyde monoterpéniques hydrocarbures sesquiterpéniques

FORM-LAB005-B Page 2 sur 9 methyl tridecane 0.020 2-nonanone 0.290 angelate d'isoamyle 0.460 angelate d'alkyle 0.02 (E)-oxyde de linalol 0.020 dimethyl-styrene 0.040 caproate d'isoamyle 0.030 angelate d'alkyle 0.1 composé aliphatique 0.020 alcool terpenique 0.150 2-decanone 0.020 decanal 0.020 isoitalicene 0.600 2-nonanol 0.07 dione 0.310 linalol * 1.560 italicene 2.22 acetate de linalyle 0.04 sesquiterpene 0.020 alcool terpenique 0.090 cis-alpha-bergamotene 0.500

FORM-LAB005-B Page 3 sur 9 alcool terpenique 0.03 epsilon cadinene + fenchol 0.06 trans alpha bergamotene 0.3 2-undecanone 0.11 3,5-dimethyloctane-4,6-dione 1.160 terpinene-4-ol 0.470 epoxyde de limonene isomere 0.030 epoxyde de limonene isomere 0.030 epi-beta-santalene 0.020 acetate terpenique 0.030 acetate terpenique 0.040 sesquiterpene 0.030 E-beta- farnesene 0.210 zonarène 0.050 sesquiterpene 0.050 alpha-humulene 0.040 gamma-selinene 0.290 curcumene isomere 0.300 (Z)-beta farnesene 0.100 gamma-curcumene + gamma-muurolene 11.200 alpha-terpineol 0.070

FORM-LAB005-B Page 4 sur 9 angelate d'alkyle + borneol 0.130 formiate de geranyle 0.030 eremophilene 0.020 (Z-E)-alpha-farnesene 0.050 acetate de neryle 33.010 alpha-muurolene + beta-selinene 0.160 alpha-selinene 0.100 geranial * 0.040 beta-curcumene 0.360 trans-piperitol 0.040 acetate de geranyle 0.140 farnesene isomere 0.090 delta-cadinene 0.030 gamma-cadinene 0.050 beta-sesquiphellandrene 0.030 alpha-bisabolene 0.05 alpha-curcumene 2.570 propionate de neryle 5.050 cadina-1,4-diene 0.040 nerol 3.070 alpha-amorphene 0.020

FORM-LAB005-B Page 5 sur 9 acetate de 2-phenylethyle 0.020 2,4-decadienal 0.020 ester terpenique 0.25 geraniol * 0.05 para-cymene-8-ol 0.020 composé Mw=220 0.100 isobutyrate de neryle 0.290 trans-myrtanol 0.04 deshydrocurcumene + composé Mw= 220 0.140 methylpropionate de neryle 0.3 nonadecane 0.070 italidione I Mw=210 8.700 italidione II Mw=224 2.540 composé aromatique 0.040 dimethyl hexene 0.180 ester insature 0.020 ester insature isomere 0.050 bornylene 0.080 methyl-2-pentanone-3 0.120 alpha-pinene 2.310 alpha-fenchene 0.420

FORM-LAB005-B Page 6 sur 9 camphene 0.190 4-methyl-3-hexanone 0.290 hexanal 0.010 beta-pinene 0.700 beta-myrcene 0.110 alpha-phellandrene 0.050 2-methylbutyrate d'isobutyle 0.040 alpha-terpinene 0.190 isoamyle isobutyrate 0.030 limonene * 4.570 arbusculone isomere 0.020 beta-phellandrene + cineole 1,8 0.560 cis-beta-ocimene 0.030 trans-arbusculone 0.04 gamma-terpinene 0.710 trans beta ocimene 0.210 para-cymene 0.26 3-methylbutyrate de 2-methylbutyle 0.080 terpinolene 0.230 angelate d'isobutyle 0.160 acetate de cis-3-hexenyle 0.020

FORM-LAB005-B Page 7 sur 9 angelate d'alkyle 0.020 6-methyl-5-hepten-2-one 0.020 tiglate d'iso-butyle 0.020 ester angelique 0.020 italidione isomere 0.210 trans jasmone 0.080 italidone III Mw=238 2.010 valerate de neryle 0.350 ester phenylethylique 0.040 methylvalerate de neryle 0.050 oxygened compound Mw=236 0.070 ether aliphatique 0.020 nerolidol 0.040 dione aliphatique 0.240 tiglate de neryle 0.070 ester benzylique 0.030 guaiol 0.860 composé cetonique 0.020 ester phenylethylique 0.020 dione aliphatique 0.350 eudesmol isomere 0.230

FORM-LAB005-B Page 8 sur 9 eudesma-5en-11-alpha-ol 1.320 benzoate de cis-3-hexenyle 0.030 sesquiterpenol 0.140 compose methoxyaromatique 0.070 ester sesquiterpenique 0.020 eudesmol isomere 0.520 gamma-eudesmol 0.250 oxygened compound Mw=236 0.030 agarospirol 0.060 sesquiterpenol 0.050 guaiol isomere 0.030 sesquiterpenol 0.140 bulnesol 0.240 valerianol 0.030 alpha-eudesmol 0.300 beta-eudesmol 0.450 acetate de farnesyle 0.080 acide caprique 0.030 composé aromatique 0.030 caryophylla-3,7-dien-6-ol 0.030 compose polyoxygene 0.020

FORM-LAB005-B Page 9 sur 9 dione aliphatique 0.060 composé sesquiterpenique 0.020 ester aliphatique 0.060 dione aliphatique 0.030 acide laurique 0.020 composé diol 0.030 Total 99.420 * = Substance(s) allergène(s) / allergen(s) ** = Substance(s) classée(s) CMR / Substance(s) classified as CMR