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T-007

Supelco

(±)-11-nor-9-Carboxy-Δ9-THC-D9 solution

100 μg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Empirical Formula (Hill Notation):
C21H19D9O4
CAS Number:
136765-52-1
Molecular Weight:
353.50
EC Number:
200-659-6
MDL number:
MFCD00673310
UNSPSC Code:
41116107
PubChem Substance ID:
329826583
NACRES:
NA.24

grade

certified reference material

Quality Level

300

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

psicótropo (Spain); Decreto Lei 15/93: Tabela IIB (Portugal)

concentration

100 μg/mL in methanol

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

cannabis testing
forensics and toxicology

format

single component solution

storage temp.

-10 to -25°C

SMILES string

OC1=C2C3C(CCC(C(O)=O)=C3)C(C([2H])([2H])[2H])(C([2H])([2H])[2H])OC2=CC(CCCCC([2H])([2H])[2H])=C1

InChI

1S/C21H28O4/c1-4-5-6-7-13-10-17(22)19-15-12-14(20(23)24)8-9-16(15)21(2,3)25-18(19)11-13/h10-12,15-16,22H,4-9H2,1-3H3,(H,23,24)/i1D3,2D3,3D3

InChI key

YOVRGSHRZRJTLZ-GQALSZNTSA-N

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General description

11-nor-9-Carboxy-Δ9-THC, also known as THC acid, is the main secondary metabolite of Δ9-THC found in urine or blood of cannabis users. This internal standard is applicable for numerous applications in GC/MS or LC/MS testing from forensic analysis and clinical toxicology to urine drug testing and isotope dilution methods.

Application

  • Hydrodesulfurization research using pharmacosiderite Mo(4)P(3)O(16): This study utilized the microporous catalytic activity of synthesized Mo(4)P(3)O(16) under moderate temperatures for hydrodesulfurization, showing its potential in refining processes relevant to forensic toxicology for substance identification, including THC metabolites (Ishikawa et al., 2024).
  • Synthesis of acyl cyclopentaquinolinones: Research demonstrated the construction of acyl cyclopentaquinolinones with potential implications for the synthesis and analysis of synthetic cannabinoids, helping to understand cannabinoid biochemistry and metabolism (Xue et al., 2024).
  • Nutraceutical applications from biomass: The production and characterization of xylooligosaccharides from lignocellulosic biomass were reviewed, relevant for cannabinoid research by providing insights into plant-derived compound processing and applications, influencing synthetic THC derivative studies (Kumar et al., 2024).
  • Adverse event detection in pharmaceutical care: This study evaluated deep learning models for detecting adverse events from pharmaceutical care records, offering a methodological approach that could be adapted for monitoring effects related to synthetic cannabinoids in clinical settings (Nishioka et al., 2024).

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

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T-004

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(±)-11-nor-9-Carboxy-Δ9-THC solution, 100 μg/mL in methanol, ampule of 1 mL, Cerilliant®

T-008

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T-011

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T-018

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T-019

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T-038

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T-080

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Kaizheng Gong et al.
Journal of hypertension, 29(9), 1810-1819 (2011-08-13)
Pharmacological activation of peroxisome proliferator-activated receptor gamma (PPARγ) has been shown to attenuate pressure overload-induced cardiac fibrosis, suggesting that PPARγ has an antifibrotic effect. This study tested the hypothesis that there is a functional interaction between transforming growth factor-β (TGF-β)

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