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Methyl-n-amylnitrosamine: Difference between revisions

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{{DISPLAYTITLE:Methyl-''n''-amylnitrosamine}} {{DISPLAYTITLE:Methyl-''n''-amylnitrosamine}}
{{orphan|date=February 2010}}
{{chembox {{chembox
| Verifiedfields = changed
⚫ | verifiedrevid = 360752413
| Watchedfields = changed
⚫ |Name=Methyl-''n''-amylnitrosamine
⚫ | verifiedrevid = 425012515
⚫ |ImageFile=Methylamylnitrosamine.png
⚫ | Name = Methyl-''n''-amylnitrosamine
⚫ |ImageSize=180px
⚫ | ImageFile = Methylamylnitrosamine.png
|IUPACName=''N''-Methyl-''N''-pentylnitrous amide
| ImageFile_Ref = {{chemboximage|correct|??}}
|OtherNames=Methylamylnitrosamine
⚫ | ImageSize = 160
| ImageName = Skeletal formula of methyl-n-amylnitrosamine
| PIN = Methyl(pentyl)nitrous amide
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| Abbreviations=MNAN
| CASNo=13256-07-0 | CASNo = 13256-07-0
| UNII_Ref = {{fdacite|correct|FDA}}
⚫ | PubChem=25805
| UNII = U9D5PXJ785
⚫ | SMILES=CCCCCN(C)N=O
⚫ | PubChem = 25805
⚫ }}
| ChemSpiderID = 24041
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| MeSHName = N-amyl-N-methylnitrosamine
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 140674
| ChEMBL = 352469
| ChEMBL_Ref = {{ebicite|changed|EBI}}
⚫ | SMILES = CCCCCN(C)N=O
| StdInChI = 1S/C6H14N2O/c1-3-4-5-6-8(2)7-9/h3-6H2,1-2H3
| StdInChI_Ref = {{chemspidercite|correct|chemspider}}
| StdInChIKey = KSFCDINBDBFFSI-UHFFFAOYSA-N
| StdInChIKey_Ref = {{chemspidercite|correct|chemspider}}
⚫ }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| C=6 | N=2 | H=14 | O=1
| Formula=C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O
| Appearance = Yellow, transparent liquid
| MolarMass=130.19 g/mol
| LogP = 1.542
| Appearance=
⚫ }}
| Density=
⚫ |Section3={{Chembox Related
| MeltingPt=
| OtherFunction_label = amines
| BoilingPt=
| OtherFunction = {{unbulleted list|]|]|]}}
| Solubility=
| OtherCompounds = ]
⚫ }}
⚫ }}
⚫ |Section3={{Chembox Hazards
| MainHazards=
| FlashPt=
| Autoignition=
⚫ }}
}} }}


'''Methyl-''n''-amylnitrosamine''' (MNAN) is a potential ]<ref>{{cite journal |author=Bulay O, Mirvish SS |title=Carcinogenesis in rat esophagus by intraperitoneal injection of different doses of methyl-n-amylnitrosamine |journal=Cancer Res. |volume=39 |issue=9 |pages=3644–6 |year=1979 |month=September |pmid=476689 |doi= |url=http://cancerres.aacrjournals.org/cgi/pmidlookup?view=long&pmid=476689}}</ref> It is metabolized in the liver by the ] ]. '''Methyl-''n''-amylnitrosamine''' (MNAN) is a potential ]<ref>{{cite journal |vauthors=Bulay O, Mirvish SS |title=Carcinogenesis in rat esophagus by intraperitoneal injection of different doses of methyl-n-amylnitrosamine |journal=Cancer Res. |volume=39 |issue=9 |pages=3644–6 |date=September 1979 |pmid=476689 |url=http://cancerres.aacrjournals.org/cgi/pmidlookup?view=long&pmid=476689}}</ref> It is metabolized in the liver by the ] ].


==References== ==References==
{{reflist}}
<references/>


] ]
] ]




Latest revision as of 21:48, 16 February 2022

Methyl-n-amylnitrosamine
Skeletal formula of methyl-n-amylnitrosamine
Skeletal formula of methyl-n-amylnitrosamine
Names
Preferred IUPAC name Methyl(pentyl)nitrous amide
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
MeSH N-amyl-N-methylnitrosamine
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H14N2O/c1-3-4-5-6-8(2)7-9/h3-6H2,1-2H3Key: KSFCDINBDBFFSI-UHFFFAOYSA-N
SMILES
  • CCCCCN(C)N=O
Properties
Chemical formula C6H14N2O
Molar mass 130.191 g·mol
Appearance Yellow, transparent liquid
log P 1.542
Related compounds
Related amines
Related compounds Agmatine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Methyl-n-amylnitrosamine (MNAN) is a potential carcinogen It is metabolized in the liver by the enzyme CYP2A6.

References

  1. Bulay O, Mirvish SS (September 1979). "Carcinogenesis in rat esophagus by intraperitoneal injection of different doses of methyl-n-amylnitrosamine". Cancer Res. 39 (9): 3644–6. PMID 476689.


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