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5957-75-5

5957-75-5 Structure

5957-75-5 Structure
IdentificationBack Directory
[Name]

DELTA-8-THC
[CAS]

5957-75-5
[Synonyms]

Δ8-THC
(-)-Δ8-THC
DELTA-8-THC
Δ8-THC (CRM)
(-)-DELTA8-THC
Methamnetamine
delta(sup6)-thc
delta(sup8)-thc
(-)-DELTA-8-THC
(-)-trans-D8-Form
6-Methoxymethylone
5-IT hemisuccinate
BMDB hydrochloride
(?)-Δ8-THC solution
N-Ethylpentylone-d5
α-PiHP hydrochloride
MBDB-d5 hydrochloride
25H-NBF hydrochloride
4-AcO-MET hemifumarate
4-Cl-IBF hydrochloride
25H-NBMD hydrochloride
4F-α-PHP hydrochloride
AM-2201-d5 (indole-d5)
4-OH-DET hydrochloride
Codeine-N-oxide hydrate
Normorphine hemihydrate
8-Tetrahydro Cannabinol
Δ6-Tetrahydrocannabinol
(±)-MDA hydrochloride-d5
AH-7921-d6 (dimethyl-d6)
Tetrahydrofuranylfentanyl
(-)-delta8-THC, 1.0 mg/mL
1-Δ8-Tetrahydrocannabinol
Δ1(6)-Tetrahydrocannabinol
Benzoylecgonine-d3 hydrate
Dibutylone-d3 hydrochloride
Codeine-{13C1} hydrochloride
Propoxyphene-d5 hydrochloride
Cocaethylene-d3 hydrochloride
DELTA(8)-TETRAHYDROCANNABINOL
Δ8-trans-Tetrahydrocannabinol
(±)-Cathinone-d5 hydrochloride
DL-Amphetamine-d5 hydrochloride
Cocaethylene-13C6 hydrochloride
6-Acetylmorphine-d3 (acetyl-d3)
(-)-DELTA8-TETRAHYDROCANNABINOL
DL-Amphetamine-d3 hydrochloride
Senecioylfentanyl hydrochloride
Benzoylecgonine-d3 hydrochloride
DL-Amphetamine-d11 hydrochloride
Morphine-3-β-D-glucuronide hydrate
2C-B-13C6 (ring 13C6) hydrochloride
2,5-Dimethoxy-4-methylmethcathinone
Lorazepam-13C6 (7-chlorobenzo-13C6)
2C-I-13C6 hydrochloride (ring 13C6)
4-Methoxyethcathinone hydrochloride
2C-H -13C6 hydrochloride (ring 13C6)
Sodium gammahydroxybutyrate-1,4-13C2
DL-Methamphetamine-d11 hydrochloride
(-)-Δ8-Tetrahydrocannabinol solution
4-Fluorobutyrylfentanyl hydrochloride
Morphine-3-β-D-glucuronide-d3 hydrate
Oxycodone-d6 hydrochloride monohydrate
4-Hydroxybutyrylfentanyl hydrochloride
Ethylone-d5 hydrochloride (N-ethyl-d5)
4-Fluorobutyrylfentanyl-d7 hydrochloride
DL-2-Methylmethamphetamine hydrochloride
4-Fluoroisobutyrylfentanyl hydrochloride
1-trans-delta(sup8)-tetrahydro-cannabino
1-trans-delta(sup8)-tetrahydrocannabinol
DL-3-Methylmethamphetamine hydrochloride
α-Pyrrolidinooctanophenone hydrochloride
DL-2-Fluoromethamphetamine hydrochloride
Cocaine-13C6 hydrochloride (benzoyl-13C6)
DL-2-Methoxymethamphetamine hydrochloride
Chlordiazepoxide-13C6 (7-chlorobenzo-13C6)
(-)-delta(sup8)-trans-tetrahydrocannabinol
(-)-trans-delta(sup8)-tetrahydrocannabinol
2,4,5-Trimethylmethcathinone hydrochloride
(-)-trans-Δ9-THC-13C4 (pentyl-2,3,4,5-13C4)
(±)-Methadone-13C6 hydrochloride (ring-13C6)
Tetramethylcyclopropanfentanyl hydrochloride
3-Acetylmorphine-d3 hydrochloride (acetyl-d3)
Benzoylecgonine-d5 hydrochloride (benzoyl-d5)
3',4'-Methylenedioxy-N-tert-butylcathinone HCl
(-)-delta(sup6)-3,4-trans-tetrahydrocannabinol
DELTA8-TETRAHYDROCANNABINOL METHANOL*SOL UTION
Codeine-6-b-D-glucuronide trifluoroacetate salt
Benzoylecgonine-13C6 tetrahydrate (benzoyl-13C6)
4-Bromo-α-pyrrolidinopropiophenone hydrochloride
delta8-tetrahydrocannabinol ethanol*solution--dea
4-Fluoro-α-pyrrolidinoheptiophenone hydrochloride
DL-Amphetamine-13C6 hemisulphate (2:1, ring-13C6)
4-Methoxy-α-pyrrolidinooctanophenone hydrochloride
4-Hydroxy-N-methyl-N-ethyltryptamine hydrochloride
4-Methoxy-α-pyrrolidinoheptiophenone hydrochloride
DL-2,5-Dimethoxy-4-fluoroamphetamine hydrochloride
Morphine-6-β-D-glucuronide-d3 (N-methyl-d3) hydrate
DELTA8-TETRAHYDROCANNABINOL ETHANOL*SOLUTION--DEA SC
Ecgonine methyl ester-d3 (N-methyl d3) hydrochloride
(-)-Heroin-d3 hydrochloride (N-methyl-d3) monohydrate
(-)-DELTA8-TETRAHYDROCANNABINOL >99% 10M G/ML ETNALOL
8-Tetrahydro Cannabinol (1 mg/mL solution in methanol)
Buprenorphine-d4 (cyclopropyl-2,2,3,3-d4) hydrochloride
Cocaine-13C6,d3 hydrochloride (benzoyl-13C6, N-methyl-d3)
DL-threo-Methylphenidate-d9 hydrochloride (piperidine-d9)
Dihydrocodeine-d6 hydrochloride (N-methyl-d3, methoxy-d3)
DL-erythro-Methylphenidate-d9 hydrochloride (piperidine-d9
Buprenorphine-d4 (cyclopropyl-2,2,3,3-d4) 3-β-D-glucuronide
4-Methylmethcathinone-13C6 hydrochloride (benzene ring-13C6)
(±)-MDMA-d5 hydrochloride (alpha-methyl-d3-ethylamine-1,2-d2)
3-amyl-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol
6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol
d)pyran-1-ol,6a,7,10,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-6h-dibenzo(
d)pyran-1-ol,6a,7,10,10a-tetrahydro-3-pentyl-6,6,9-trimethyl-6h-dibenzo(tr
(6aR)-6a,7,10,10aα-Tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol
6H-Dibenzo[b,d]pyran-1-ol, 6a,7,10,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-, (6aR,10aR)-
[EINECS(EC#)]

637-364-0
[Molecular Formula]

C21H30O2
[MDL Number]

MFCD00083206
[MOL File]

5957-75-5.mol
[Molecular Weight]

314.46
Chemical PropertiesBack Directory
[alpha ]

D18 -264° (c = 0.11 in ethanol)
[Boiling point ]

bp0.001 200°
[density ]

1.0536 (rough estimate)
[refractive index ]

1.5404 (estimate)
[Fp ]

11 °C
[storage temp. ]

−20°C
[solubility ]

DMF: 50 mg/ml
DMF: PBS (pH 7.2)(1:3): 250 µg/ml
DMSO: 60 mg/ml
Ethanol: 35 mg/ml
Methanol: 30 mg/ml
[form ]

ethanol solution
[pka]

9.83±0.60(Predicted)
Safety DataBack Directory
[Hazard Codes ]

F,T
[Risk Statements ]

11-39/23/24/25-23/24/25
[Safety Statements ]

7-16-36/37-45
[RIDADR ]

UN 1170 3/PG 2
[WGK Germany ]

1
[Toxicity]

LD50 i.v. in mice: 27.5 mg/kg (Yoshimura)
Hazard InformationBack Directory
[Uses]

It is one of the active constituent of cannabis. Agonist at CB1 and CB2 cannabinoid receptors. Antiemetic; appetite stimulant. Controlled substance (hallucinogen).
[Definition]

ChEBI: Delta8-THC is a 1-benzopyran.
[References]

[1] MATHANGI KRISHNAMURTHY  Bob M I M  Antonio M Ferreira. Synthesis and Testing of Novel Phenyl Substituted Side-Chain Analogues of Classical Cannabinoids.[J]. ChemInform, 2004, 35 4. DOI: 10.1002/chin.200404143
[2] DINESH THAPA. The Cannabinoids Δ8THC, CBD, and HU-308 Act via Distinct Receptors to Reduce Corneal Pain and Inflammation.[J]. Cannabis and Cannabinoid Research, 2018, 3 1: 11-20. DOI: 10.1089/can.2017.0041
[3] LIESL K. JANSSENS. Investigation of the intrinsic cannabinoid activity of hemp-derived and semisynthetic cannabinoids with β-arrestin2 recruitment assays—and how this matters for the harm potential of seized drugs[J]. Archives of Toxicology, 2024, 98 8: 2619-2630. DOI: 10.1007/s00204-024-03769-4
[4] JOHN MERRICK. Identification of Psychoactive Degradants of Cannabidiol in Simulated Gastric and Physiological Fluid.[J]. Cannabis and Cannabinoid Research, 2016, 1 1: 102-112. DOI: 10.1089/can.2015.0004
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