Hygrine

Names
Preferred IUPAC name

1-[(2R)-1-Methylpyrrolidin-2-yl]propan-2-one

Identifiers

CAS Number

* 496-49-1 Y

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:46750 Y

ChemSpider |

* 389762 Y

KEGG |

* C06179 Y

PubChem CID

* 440933

UNII |

* 49H1LNM62X Y

InChI

* InChI=1S/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1 Y

Key: ADKXZIOQKHHDNQ-MRVPVSSYSA-N Y

* 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).

Y verify (what is YN ?)
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.

## See also

* Coca alkaloids
* Pseudotropine
* Troparil

## 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.". http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE. Retrieved July 15, 2005.

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*[CID]: Compound ID