Water Activity Date/Time Extracted: 12/29/16 17:20
Analysis Method/SOP: 102
Date/Time Analyzed: 12/29/16 17:20
Water Activity: 0.532 at 24°C
Moisture Date/Time Extracted: 12/30/16 00:00
Analysis Method/SOP: 103
Date/Time Analyzed: 12/30/16 00:00
Moisture: 6.25 %
Eric Wendt Chief Science Officer - 1/13/2017 All QC samples met acceptance criteria of the method; data available upon request. These results relate only to the sample included on this report. The report may not be reproduced except in full, without the written permission of Green Leaf Lab.
0.000 CBG
CBC
0
Official Cannalysis Report Green Leaf Lab proudly follows TNI 2009 Quality Standards
12025 NE Marx St. Portland, OR 97220 503-253-3511 / www.greenleaflab.org
About your terpene profile Terpenes are aromatic molecules found in plant resins. They are not only responsible for the many unique smells of Cannabis, but they accentuate the holistic effect of cannabanoids as well. Terpene profiles can be utilized to quantify strong flavor, identify different strains and achieve therapeutic benefits. Green Leaf Lab’s terpene analysis quantifies the 25 most common terpenes found in Cannabis sativa. Terpenes are generally divided into two chemical classifications: Monoterprens and sesquiterpenes. Monoterpenes: All of the monoterpenes are very similar in chemical structure, containing 10 carbons and 6 hydrogens. Although, they are similar, the varying arrangements produce distinct aromas. Changes such as oxidation and rerrangement produce monoterpenoids which will have a different chemical formula. Monoterpenes are more volatile than sesquiterpenes; the aromas tend to be stronger and they are more prone to being lost by heating and oxidation. Myrcene and Limonene are examples of an acyclic and cyclic monoterpene, respectively. They both share a basic structure containing a backbone of 10 carbon atoms, however arranged uniquely. Sesquiterpenes: The sesquiterpenes are a more complex class of terpenes. They are also generally aromatic, but are also heavier and less volatile. Thus, they often remain after some of the more volatile monoterpenes have broken down under heat or oxidation.
Eric Wendt Chief Science Officer - 1/13/2017 All QC samples met acceptance criteria of the method; data available upon request. These results relate only to the sample included on this report. The report may not be reproduced except in full, without the written permission of Green Leaf Lab.
Official Cannalysis Report Green Leaf Lab proudly follows TNI 2009 Quality Standards
12025 NE Marx St. Portland, OR 97220 503-253-3511 / www.greenleaflab.org
Eric Wendt Chief Science Officer - 1/13/2017 All QC samples met acceptance criteria of the method; data available upon request. These results relate only to the sample included on this report. The report may not be reproduced except in full, without the written permission of Green Leaf Lab.
0.7
0.8
Official Cannalysis Report Green Leaf Lab proudly follows TNI 2009 Quality Standards
12025 NE Marx St. Portland, OR 97220 503-253-3511 / www.greenleaflab.org
Date Sampled: 12/22/16 00:00
Dutch Treat
Date Accepted: 12/22/16
Summit Cannabis LLC
Results Valid Until: 12/22/17
Sample ID: G6L0281-01
Matrix: Useable Marijuana
Metrc ID: 1A4010300001134000000040
Pesticide Analysis in ppm Date/Time Extracted: 01/12/17 09:59
Date/Time GC Analyzed: 01/13/17 01:39
Analysis Method/SOP: 203
Date/Time LC Analyzed: 01/13/17 02:01
Analyte
Type
AL
Result
Analyte
Type
AL
Result
Abamectin
I
0.5
< LOQ
Acephate
Organophosphate Insecticide
0.4
< LOQ
Acequinocyl
I
2
< LOQ
Acetamiprid
Neonicotinoid instecticide
0.2
< LOQ
Aldicarb
Carbamate insecticide
0.4
< LOQ
Azoxystrobin
F
0.2
< LOQ
Bifenazate
Unclassified insecticide
0.2
< LOQ
Bifenthrin
PYR
0.2
< LOQ
Boscalid
Anilide fungicide
0.4
< LOQ
Carbaryl
Carbamate insecticide
0.2
< LOQ
Carbofuran
Carbamate insecticide
0.2
< LOQ
Chlorantraniliprole
Anthranilic diamide insecticide
0.2
< LOQ
Chlorfenapyr
Pyrazole insecticide
1
< LOQ
Chlorpyrifos
Organophosphate Insecticide
0.2
< LOQ
Clofentezine
I
0.2
< LOQ
Cyfluthrin
I
1
< LOQ
Cypermethrin
PYR
1
< LOQ
Daminozide
I
1
< LOQ
DDVP (Dichlorvos)
I
1
< LOQ
Diazinon
Organophosphate Insecticide
0.2
< LOQ
Dimethoate
I
0.2
< LOQ
Ethoprophos
I
0.2
< LOQ
Etofenprox
I
0.4
< LOQ
Etoxazole
Unclassified miticide
0.2
< LOQ
Fenoxycarb
I
0.2
< LOQ
Fenpyroximate
I
0.4
< LOQ
Fipronil
Pyrazole insecticide
0.4
< LOQ
Flonicamid
Pyridinecarboxamide insecticide
1
< LOQ
Fludioxonil
non-systemic fungicide
0.4
< LOQ
Hexythiazox
I
1
< LOQ
Imazalil
Azole fungicide
0.2
< LOQ
Imidacloprid
Neonicotinoid insectide
0.4
< LOQ
Kresoxim-methyl
I
0.4
< LOQ
Malathion
I
0.2
< LOQ
Metalaxyl
I
0.2
< LOQ
Methiocarb
Carbamate insecticide
0.2
< LOQ
Methomyl
Carbamate insecticide
0.4
< LOQ
Methyl parathion
I
0.2
< LOQ
MGK-264
I
0.2
< LOQ
Myclobutanil
Azole fungicide
0.2
< LOQ
Naled
I
0.5
< LOQ
Oxamyl
Carbamate insecticide
1
< LOQ
Paclobutrazol
Azole plant growth regulator
0.4
< LOQ
Permethrins
I
0.2
< LOQ
Phosmet
Organophosphate insecticide
0.2
< LOQ
Piperonyl butoxide
SYN
2
< LOQ
Prallethrin
I
0.2
< LOQ
Propiconazole
I
0.4
< LOQ
Propoxur
Carbamate insecticide
0.2
< LOQ
Pyrethrins
I
1
< LOQ
Pyridaben
Unclassified insecticide
0.2
< LOQ
Spinosad
Spinosyn insecticide
0.2
< LOQ
Spiromesifen
Keto-enol insecticide
0.2
< LOQ
Spirotetramat
Keto-enol insecticide
0.2
< LOQ
Spiroxamine
Unclassified fungicide
0.4
< LOQ
Tebuconazole
F
0.4
< LOQ
Thiacloprid
I
0.2
< LOQ
Thiamethoxam
Neonicotinoid insectide
0.2
< LOQ
Trifloxystrobin
Strobin fungicide
0.2
< LOQ
Eric Wendt Chief Science Officer - 1/13/2017 All QC samples met acceptance criteria of the method; data available upon request. These results relate only to the sample included on this report. The report may not be reproduced except in full, without the written permission of Green Leaf Lab.
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