| Revision as of 13:49, 2 May 2011 editLuckas-bot (talk | contribs)929,662 editsm r2.7.1) (robot Adding: ja:ノイリン← Previous edit |
Latest revision as of 23:58, 7 April 2022 edit undoCitation bot (talk | contribs)Bots5,460,414 edits Add: authors 1-1. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Headbomb | Linked from Misplaced Pages:WikiProject_Academic_Journals/Journals_cited_by_Wikipedia/Sandbox | #UCB_webform_linked 139/207 |
| (15 intermediate revisions by 14 users not shown) |
| Line 1: |
Line 1: |
|
{{chembox |
|
{{chembox |
|
|
| Verifiedfields = changed |
| ⚫ |
| verifiedrevid = 265832580 |
|
|
|
| Watchedfields = changed |
| ⚫ |
| ImageFile = Neurine.png |
|
|
⚫ |
| verifiedrevid = 427065934 |
|
⚫ |
| ImageFile = Neurine Structural Formula V1.svg |
|
| ImageSize = 150px |
|
| ImageSize = 150px |
|
| IUPACName = Trimethylvinylammonium hydroxide |
|
| IUPACName = Trimethylvinylammonium hydroxide |
|
| OtherNames = Vitaloid; ''N,N,N''-Trimethylethenaminium hydroxide |
|
| OtherNames = Vitaloid; ''N,N,N''-Trimethylethenaminium hydroxide |
|
| Section1 = {{Chembox Identifiers |
|
|Section1={{Chembox Identifiers |
|
|
| CASNo_Ref = {{cascite|correct|??}} |
|
| CASNo = 463-88-7 |
|
|
| PubChem = 10042 |
|
| CASNo = 463-88-7 |
|
|
| UNII_Ref = {{fdacite|correct|FDA}} |
| ⚫ |
| SMILES = C=C(C)(C)C. |
|
|
|
| UNII = G6RL36OO0J |
|
|
| PubChem = 10042 |
|
⚫ |
| SMILES = C=C(C)(C)C. |
|
|
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
|
|
| ChemSpiderID = 9647 |
|
|
| InChI = 1/C5H12N.H2O/c1-5-6(2,3)4;/h5H,1H2,2-4H3;1H2/q+1;/p-1 |
|
|
| InChIKey = NIPLIJLVGZCKMP-REWHXWOFAL |
|
|
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChI = 1S/C5H12N.H2O/c1-5-6(2,3)4;/h5H,1H2,2-4H3;1H2/q+1;/p-1 |
|
|
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
|
|
| StdInChIKey = NIPLIJLVGZCKMP-UHFFFAOYSA-M |
|
}} |
|
}} |
|
| Section2 = {{Chembox Properties |
|
|Section2={{Chembox Properties |
|
| Formula = C<sub>5</sub>H<sub>13</sub>NO |
|
| Formula = C<sub>5</sub>H<sub>13</sub>NO |
|
| MolarMass = 103.16 |
|
| MolarMass = 103.16 |
|
| Appearance = Syrupy liquid |
|
| Appearance = Syrupy liquid |
|
| Density = |
|
| Density = |
|
| MeltingPt = |
|
| MeltingPt = |
|
| BoilingPt = |
|
| BoilingPt = |
|
| Solubility = Soluble |
|
| Solubility = Soluble |
|
}} |
|
}} |
|
| Section3 = {{Chembox Hazards |
|
|Section3={{Chembox Hazards |
|
| MainHazards = |
|
| MainHazards = |
|
| FlashPt = |
|
| FlashPt = |
|
| Autoignition = |
|
| AutoignitionPt = |
|
}} |
|
}} |
|
}} |
|
}} |
| Line 28: |
Line 41: |
|
'''Neurine''' is an ] found in egg yolk, brain, bile and in cadavers. It is formed during putrefaction of biological tissues by the ] of ]. It is a poisonous, syrupy liquid with a fishy odor. |
|
'''Neurine''' is an ] found in egg yolk, brain, bile and in cadavers. It is formed during putrefaction of biological tissues by the ] of ]. It is a poisonous, syrupy liquid with a fishy odor. |
|
|
|
|
|
Neurine is a ] with three ] groups and one ] group attached to the nitrogen atom. Synthetically, neurine can be prepared by the reaction of ] with ]. Neurine is unstable and decomposes readily to form trimethylamine. |
|
Neurine is a ] with three ] groups and one ] attached to the nitrogen atom. Synthetically, neurine can be prepared by the reaction of ] with ].<ref>{{Cite journal|last1=Gardner|first1=C.|last2=Kerrigan|first2=V.|last3=Rose|first3=J. D.|last4=Weedon|first4=B. C. L.|date=1949-01-01|title=169. Acetylene reactions. Part IV. Formation of trimethylvinyl- and tetramethyl-ammonium hydroxide from acetylene and aqueous trimethylamine|url=https://pubs.rsc.org/en/content/articlelanding/1949/jr/jr9490000789|journal=Journal of the Chemical Society (Resumed)|language=en|pages=789–792|doi=10.1039/JR9490000789|issn=0368-1769}}</ref> Neurine is unstable and decomposes readily to form trimethylamine. |
|
|
|
|
|
==References== |
|
==References== |
|
|
{{Reflist}} |
|
*''Merck Index'', 11th Edition, '''6393'''. |
|
*''Merck Index'', 11th Edition, '''6393'''. |
|
|
|
|
|
] |
|
] |
|
] |
|
] |
|
|
] |
|
|
|
|
] |
|
|
] |
|