Hygrine

Hygrine
Names
	IUPAC name (R)-1-(1-Methylpyrrolidin-2-yl)-propan-2-one
Identifiers
CAS Number	496-49-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:46750 ;
ChemSpider	389762 ;
ECHA InfoCard	100.007.112
KEGG	C06179 ;
PubChem CID	440933;
UNII	49H1LNM62X ;
CompTox Dashboard (EPA)	DTXSID40894081 ;
	InChI InChI=1S/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1 Key: ADKXZIOQKHHDNQ-MRVPVSSYSA-N ; InChI=1/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1 Key: ADKXZIOQKHHDNQ-MRVPVSSYBT;
	SMILES CC(=O)C[C@H]1CCCN1C;
Properties
Chemical formula	C8H15NO
Molar mass	141.21 g/mol
Boiling point	193 to 195 °C (379 to 383 °F; 466 to 468 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Hygrine is a pyrrolidine alkaloid, found mainly in coca leaves (0.2%). It was first isolated by Carl Liebermann in 1889 (along with a related compound cuscohygrine) as an alkaloid accompanying cocaine in coca. Hygrine is extracted as a thick yellow oil, having a pungent taste and odor.

References

Dr. Ame Pictet (1904). The Vegetable Alkaloids. With particular reference to their chemical constitution. London: Chapman & Hall.
"Hygrine". Webster's Revised Unabridged Dictionary (? ed.). 1913.
"USDA, ARS, National Genetic Resources Program. Phytochemical and Ethnobotanical Databases. National Germplasm Resources Laboratory, Beltsville, Maryland". Archived from the original on December 11, 2012. Retrieved July 15, 2005.

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Hygrine

See also

References