Effects of the storage conditions on the stability of natural and synthetic cannabis in biological matrices for forensic toxicology analysis: An update from the literature

Promoxolane
Clinical data
Routes of; administration	By mouth
ATC code	none;
Identifiers
	IUPAC name 2,2-diisopropyl-4-hydroxymethyl-1,3-dioxolane;
CAS Number	470-43-9 ;
PubChem CID	10105;
ChemSpider	9701;
UNII	JHI9RRY52E;
ChEBI	CHEBI:134836;
ChEMBL	ChEMBL2104577;
CompTox Dashboard (EPA)	DTXSID40861970 ;
Chemical and physical data
Formula	C10H20O3
Molar mass	188.267 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(C)C1(OCC(O1)CO)C(C)C;
	InChI InChI=1S/C10H20O3/c1-7(2)10(8(3)4)12-6-9(5-11)13-10/h7-9,11H,5-6H2,1-4H3; Key:HHFOOWPWAXNJNY-UHFFFAOYSA-N;
	(verify)

Promoxolane (Dimethylane) is a centrally acting muscle relaxant and anxiolytic drug.^[1]^[2]^[3]

References

^ Rickels K (February 1968). "Drug use in outpatient treatment". The American Journal of Psychiatry. 124 (8): Suppl:20–31. doi:10.1176/ajp.124.8S.20. PMID 4865730.
^ Weiss JM, Flynn TT, Counts RM (November 1957). "Dimethylane in the treatment of anxiety reactions". Diseases of the Nervous System. 18 (11): 434–9. PMID 13473685.
^ Meltzer RI, Lewis AD, Volpe J, Lustgarten DM (May 1960). "2, 2-Disubstituted 1, 3-Dioxolanes and 2, 2-Disubstituted 1, 3-Dioxanes". The Journal of Organic Chemistry. 25 (5): 712–5. doi:10.1021/jo01075a009.

Clinical data

Routes of administration	By mouth
ATC code	none
Identifiers
IUPAC name 2,2-diisopropyl-4-hydroxymethyl-1,3-dioxolane
CAS Number	470-43-9^Y
PubChem CID	10105
ChemSpider	9701
UNII	JHI9RRY52E
ChEBI	CHEBI:134836
ChEMBL	ChEMBL2104577
CompTox Dashboard (EPA)	DTXSID40861970
Chemical and physical data
Formula	C₁₀H₂₀O₃
Molar mass	188.267 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES CC(C)C1(OCC(O1)CO)C(C)C
InChI InChI=1S/C10H20O3/c1-7(2)10(8(3)4)12-6-9(5-11)13-10/h7-9,11H,5-6H2,1-4H3 Key:HHFOOWPWAXNJNY-UHFFFAOYSA-N
(verify)