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{{chembox |
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{{chembox |
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| Verifiedfields = changed |
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| Watchedfields = changed |
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| verifiedrevid = 400113025 |
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| verifiedrevid = 443865442 |
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| Name = Hygrine |
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| Name = Hygrine |
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| IUPACName = (R)-1- (1-methylpyrrolidin- 2-yl)- propan- 2-one |
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| PIN = 1-propan-2-one |
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| ImageFile = Hygrine hr.png |
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| ImageFile = Hygrine Structural Formula V.1.svg |
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| ImageName = Chemical structure of hygrine |
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| ImageName = Chemical structure of hygrine |
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| ImageFile1 = Hygrine ball-and-stick.png |
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| Section1 = {{Chembox Identifiers |
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| ImageName1 = Ball-and-stick model of hygrine molecule |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 389762 |
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| ChemSpiderID = 389762 |
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| PubChem = 440933 |
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| PubChem = 440933 |
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| KEGG_Ref = {{keggcite|changed|kegg}} |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = C06179 |
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| KEGG = C06179 |
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| InChI = 1/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1 |
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| InChI = 1/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = ADKXZIOQKHHDNQ-MRVPVSSYSA-N |
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| StdInChIKey = ADKXZIOQKHHDNQ-MRVPVSSYSA-N |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo = 496-49-1 |
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| CASNo = 496-49-1 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| ChEBI = 46750 |
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| UNII = 49H1LNM62X |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 46750 |
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| SMILES = CC(=O)C1CCCN1C |
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| SMILES = CC(=O)C1CCCN1C |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| Formula = C<sub>8</sub>H<sub>15</sub>NO |
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| Formula = C<sub>8</sub>H<sub>15</sub>NO |
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| MolarMass = 141.21 g/mol |
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| MolarMass = 141.21 g/mol |
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| MeltingPt = |
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| MeltingPt = |
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| BoilingPt = 193-195 °C |
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| BoilingPtC = 193 to 195 |
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| Density = }} |
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| BoilingPt_notes = |
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| Density = |
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'''Hygrine''' is a ] ], found mainly in ] leaves (0.2%). It was first isolated by ] in 1889 (along with a related compound ]) as an alkaloid accompanying ] in coca. Hygrine is extracted as a thick yellow oil, having a pungent taste and odor. |
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'''Hygrine''' is a ] ], found mainly in ] leaves (0.2%). It was first isolated by ] in 1889 (along with a related compound ]) as an alkaloid accompanying ] in coca. Hygrine is extracted as a thick yellow oil, having a pungent taste and odor. |
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==References== |
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== See also == |
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* ]s |
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== References == |
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{{reflist}} |
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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= }} |
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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= }} |
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* {{cite encyclopedia | ency=Webster's Revised Unabridged Dictionary | year=1913 | edition=? | article=Hygrine}} |
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* {{cite encyclopedia | encyclopedia=Webster's Revised Unabridged Dictionary | year=1913 | edition=? | article=Hygrine}} |
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* {{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}} |
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* {{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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