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Revision as of 08:09, 21 November 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'CASNo_Ref') per Chem/Drugbox validation (report errors or [[user talk:Che...← Previous edit Revision as of 20:32, 9 February 2012 edit undoOst316 (talk | contribs)Extended confirmed users, Pending changes reviewers86,492 editsm →References: clean up, replaced: ency= → encyclopedia= using AWBNext edit →
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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 | ency=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.<nowiki></nowiki> National Germplasm Resources Laboratory, Beltsville, Maryland. | url=http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE | accessdate=July 15, 2005}} * {{cite web | title=USDA, ARS, National Genetic Resources Program. Phytochemical and Ethnobotanical Databases.<nowiki></nowiki> National Germplasm Resources Laboratory, Beltsville, Maryland. | url=http://sun.ars-grin.gov:8080/npgspub/xsql/duke/chemdisp.xsql?chemical=HYGRINE | accessdate=July 15, 2005}}


Revision as of 20:32, 9 February 2012

Hygrine
Chemical structure of hygrine
Names
IUPAC name (R)-1- (1-methylpyrrolidin- 2-yl)- propan- 2-one
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.007.112 Edit this at Wikidata
KEGG
PubChem CID
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 193-195 °C
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.

References

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