2-Methyl-2-propyl-1,3-propanediol

2-Methyl-2-propyl-1,3-propanediol
Identifiers
	IUPAC name 2-methyl-2-propyl-1,3-propanediol;
CAS Number	78-26-2;
PubChem CID	66220;
ChemSpider	59605;
UNII	YLM5KRU0P4;
CompTox Dashboard (EPA)	DTXSID9058814 ;
ECHA InfoCard	100.001.000
Chemical and physical data
Formula	C7H16O2
Molar mass	132.203 g·mol−1
3D model (JSmol)	Interactive image;
Melting point	56–59 °C (133–138 °F)
	SMILES CCCC(C)(CO)CO;
	InChI InChI=1S/C7H16O2/c1-3-4-7(2,5-8)6-9/h8-9H,3-6H2,1-2H3; Key:JVZZUPJFERSVRN-UHFFFAOYSA-N;

2-Methyl-2-propyl-1,3-propanediol (MPP) is a simple alkyl diol which has sedative, anticonvulsant and muscle relaxant effects. It is both a synthetic precursor to, and an active metabolite of the tranquilizers meprobamate and carisoprodol, as well as other derivatives.^[1]^[2]^[3]^[4]

References

↑ Wang G, Lu Q (October 2013). "A nitrate ester of sedative alkyl alcohol improves muscle function and structure in a murine model of Duchenne muscular dystrophy". Molecular Pharmaceutics. 10 (10): 3862–70. doi:10.1021/mp400310r. PMID 23924275.
↑ Yale HL, Pribyl EJ, Braker W, Bergeim FH, Lott WA (August 1950). "Muscle-relaxing Compounds Similar to 3-(o-Toloxy)-1, 2-propanediol. 1 I. Aromatic Ethers of Polyhydroxy Alcohols and Related Compounds". Journal of the American Chemical Society. 72 (8): 3710–6. doi:10.1021/ja01164a108.
↑ JP 09031000, Kato K, Tsukamoto K, "2-(2-Alkenyl)-1,3-propanediols and preparation of 2,2-disubstituted-1,3-propanediols", issued 1997
↑ Kaithal A, Hölscher M, Leitner W (October 2018). "Catalytic Hydrogenation of Cyclic Carbonates using Manganese Complexes". Angewandte Chemie International Edition in English. 57 (41): 13449–13453. doi:10.1002/anie.201808676. PMC 6221167. PMID 30134081.

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