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* {{cite book | author=Dr. Ame Pictet | title=The Vegetable Alkaloids. With particular reference to their chemical constitution | publisher=Chapman & Hall | location=London | year=1904 | id= }} * {{cite book | author=Dr. Ame Pictet | title=The Vegetable Alkaloids. With particular reference to their chemical constitution | publisher=Chapman & Hall | location=London | year=1904 | id= }}
* {{cite encyclopedia | encyclopedia=Webster's Revised Unabridged Dictionary | year=1913 | edition=? | article=Hygrine}} * {{cite encyclopedia | encyclopedia=Webster's Revised Unabridged Dictionary | year=1913 | edition=? | article=Hygrine}}
* {{cite web|title=USDA, ARS, National Genetic Resources Program. Phytochemical and Ethnobotanical Databases. National Germplasm Resources Laboratory, Beltsville, Maryland. |url=http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE |archive-url=https://archive.is/20121211210941/http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE |url-status=dead |archive-date=December 11, 2012 |accessdate=July 15, 2005 }} * {{cite web|title=USDA, ARS, National Genetic Resources Program. Phytochemical and Ethnobotanical Databases. National Germplasm Resources Laboratory, Beltsville, Maryland. |url=http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE |archive-url=https://archive.today/20121211210941/http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE |url-status=dead |archive-date=December 11, 2012 |accessdate=July 15, 2005 }}


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Latest revision as of 02:18, 4 December 2021

Hygrine
Chemical structure of hygrine
Ball-and-stick model of hygrine molecule
Names
Preferred IUPAC name 1-propan-2-one
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.007.112 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1Key: ADKXZIOQKHHDNQ-MRVPVSSYSA-N
  • InChI=1/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1Key: ADKXZIOQKHHDNQ-MRVPVSSYBT
SMILES
  • CC(=O)C1CCCN1C
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 , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

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

References

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