31262-37-0

Basic information

• Product Name: DELTA9-TETRAHYDROCANNABIVARIN
• Synonyms: N-PROPYL-DELTA9-TETRAHYDROCANNABINOL;DELTA9-TETRAHYDROCANNABIVARIN;(6aR)-3-Propyl-6,6,9-trimethyl-6aβ,7,8,10aα-tetrahydro-6H-dibenzo[b,d]pyran-1-ol;[6aR,(-)]-6aβ,7,8,10aα-Tetrahydro-6,6,9-trimethyl-3-propyl-6H-dibenzo[b,d]pyran-1-ol;Δ1-Tetrahydrocannabidivarol;Δ9-Tetrahydrocannabivarin;Δ9-Tetrahydrocannabivarol;Δ9-trans-Tetrahydrocannabivarin
• CAS NO: 31262-37-0
• Molecular Formula: C₁₉H₂₆O₂
• Molecular Weight: 286.41
• Mol File: 31262-37-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 360.6°Cat760mmHg
• Flash Point: 137.6°C
• Appearance: /
• Density: 1.034g/cm³
• Vapor Pressure: 1.06E-05mmHg at 25°C
• Refractive Index: 1.535
• PKA: 9.79±0.60(Predicted)
• CAS DataBase Reference: DELTA9-TETRAHYDROCANNABIVARIN(CAS DataBase Reference)
• NIST Chemistry Reference: DELTA9-TETRAHYDROCANNABIVARIN(31262-37-0)
• EPA Substance Registry System: DELTA9-TETRAHYDROCANNABIVARIN(31262-37-0)

Safety Data

• Hazardous Substances Data: 31262-37-0(Hazardous Substances Data)

Usage

Description

Tetrahydrocannabivarin (CRM) (Item No. 18091) is a certified reference material categorized as a phytocannabinoid. This product is intended for research and forensic applications.

InChI:InChI=1/C19H26O2/c1-5-6-13-10-16(20)18-14-9-12(2)7-8-15(14)19(3,4)21-17(18)11-13/h9-11,14-15,20H,5-8H2,1-4H3/t14-,15-/m1/s1

Upstream product

• 64898-06-2 (6aR,10aR)-1-Hydroxy-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-2-carboxylic acid methyl ester 
• 861892-40-2 (4R)-1-methyl-4-(2-(1-propylene))-2-cyclohexene-2-ol 
• 24274-48-4 cannabidivarin 
• 55382-52-0 2,4-dihydroxy-6-n-propylbenzoic acid, methyl ester 
• 1179328-06-3 Δ9-tetrahydrocannabivarin tosylate 
• 500-49-2 5-propyl-1,3-benzenediol 
• 20053-40-1 cis-Δ²-p-menthene-1,8-diol 

Downstream Products

• 1179328-06-3 Δ9-tetrahydrocannabivarin tosylate 
• 33745-21-0 cannabivarin 
• 96912-65-1 Δ⁹-tetrahydrocannabivarin-11-oic acid 

Relevant articles and documents

CATALYTIC CANNABINOID PROCESSES AND PRECURSORS

The present disclosure relates to new cannabinoid sulfonate esters and processes for their use to prepare cannabinoids. The disclosure also relates to the use of catalysts and catalytic processes for the preparation of cannabinoids from the cannabinoid sulfonate esters.

METHOD FOR PURIFYING CANNABINOID COMPOUNDS

The present invention relates to methods for purifying one or two cannabinoid compounds using simulated moving bed chromatography, wherein the cannabinoid compound(s) is/are obtained in the extract and/or the raffinate with the total amount of isomeric impurities being below detection level. In particular, the present invention relates to methods for the purification of cannabidiol, trans-(-)-delta-9-tetrahydrocannabinol, cannabidivarin, trans-(-)-delta-9-tetrahydrocannabivarin and cannabigerol which have been obtained by enantiopure synthesis.

Cannabis. X. The isolation and structures of four new propyl cannabinoid acids, tetrahydrocannabivarinic acid, cannabidivarinic acid, cannabichromevarinic acid and cannabigerovarinic acid, from Thai cannabis, Meao Variant

Four new cannabinoids acids, tetrahydrocannabivarinic acid, cannabidivarinic acid, cannabichromevarinic acid and cannabigerovarinic acid were isolated from Thai Cannabis 'Meao variant' and these structures were elucidated on the basis of chemical and spectral data. This is the first example of the isolation of propyl cannabinoid acid from Cannabis.