Identification | Back Directory | [Name]
II-NOR-9-TETRAHYDROCANNABINOL-9-CARBOXYL IC ACID (THC-COOH) (5 | [CAS]
23978-85-0 | [Synonyms]
THCA-A Thc-9-cooh THCA-A (CRM) Dea no. 7370 9-Carboxy-thc Tetrahydrocannabinols 9-Carboxy-delta(9)-thc THCA-A (exempt preparation) delta(9)-tetrahydrocannabinolic acid delta-9-Tetrahydrocannabinolic acid A Δ9-Tetrahydrocannabinolic acid A
Delta9-Tetrahydrocannabinolic acid A solution Δ9-Tetrahydrocannabinolic Acid A (1.0 mg/ml in Acetonitrile) II-NOR-9-TETRAHYDROCANNABINOL-9-CARBOXYL IC ACID (THC-COOH) (5 (6aR,10aR)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromene-2-carboxylic acid 6H-Dibenzo(B,D)pyran-2-carboxylic acid, 6A,7,8,10A-tetrahydro-1-hydroxy-6,6,9-trimethyl-3-pentyl-, (6ar,10ar)- 6H-Dibenzo(B,D)pyran-2-carboxylic acid, 6abeta,7,8,10A-tetrahydro-1-hydroxy-6,6,9-trimethyl-3-pentyl-, (6ar-trans)- | [Molecular Formula]
C22H30O4 | [MDL Number]
MFCD20133805 | [MOL File]
23978-85-0.mol | [Molecular Weight]
358.47 |
Chemical Properties | Back Directory | [Melting point ]
70 °C (decomp) | [Boiling point ]
436.8±45.0 °C(Predicted) | [density ]
1.112±0.06 g/cm3(Predicted) | [Fp ]
2℃ | [storage temp. ]
-20°C | [solubility ]
DMF: 50 mg/ml; DMF:PBS (pH 7.2) (1:3): 0.25 mg/ml; DMSO: 60 mg/ml; Ethanol: 35 mg/ml; Methanol: 30 mg/ml | [form ]
neat | [pka]
3.32±0.60(Predicted) |
Hazard Information | Back Directory | [Uses]
Delta9-Tetrahydrocannabinolic acid A solution (THCA-A,23978-85-0) is a non-psychoactive acidic cannabinoid found in cannabis with anti-inflammatory, neuroprotective, and anticancer effects. It is also the precursor to the major psychoactive cannabinoid found in cannabis, known as Δ-9-tetrahydrocannabinol (Δ-9-THC). Δ9-Tetrahydrocannabinol (THC) is a quantitative analyte that can be used for oral fluid cannabinoid monitoring.THCA-A is available as a DEA-exempt preparation and is registered as a Canadian test kit. It is primarily used in chemical analysis studies and forensics.
| [Definition]
ChEBI: A diterpenoid that is 6a,7,8,10a-tetrahydro-6H-benzo[c]chromene substituted at position 1 by a hydroxy group, positions 6, 6 and 9 by methyl groups and at position 3 by a pentyl group. A biosynthetic precursor to Delt
9-tetrahydrocannabinol, the principal psychoactive constituent of the cannabis plant. |
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