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Details

Stereochemistry ACHIRAL
Molecular Formula C5H11N
Molecular Weight 85.1475
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-METHYLPYRROLIDINE

SMILES

CN1CCCC1

InChI

InChIKey=AVFZOVWCLRSYKC-UHFFFAOYSA-N
InChI=1S/C5H11N/c1-6-4-2-3-5-6/h2-5H2,1H3

HIDE SMILES / InChI

Molecular Formula C5H11N
Molecular Weight 85.1475
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
O-Phosphonatomethylcholine, its analogues, alkyl esters, and their biological activity.
2001 Dec 6
Studies on a soft glycopyrrolate analog, SG-1.
2002 Feb
N-methylpiperidinemethyl, N-methylpyrrolidyl and N-methylpyrrolidinemethyl esters as PET radiotracers for acetylcholinesterase activity.
2003 Apr
A new highly asymmetric chelation-controlled heck arylation.
2003 Mar 26
A simple and sensitive GC method for determination of N-methylpyrrolidine in cefepime and its preparation.
2003 Nov 24
N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices.
2003 Sep
Nicotine-related alkaloids and metabolites as inhibitors of human cytochrome P-450 2A6.
2004 Feb 15
Molecular dissection of tropisetron, an alpha7 nicotinic acetylcholine receptor-selective partial agonist.
2005 Apr 22
Synthesis of new, potent avermectin-like insecticidal agents.
2005 Jul 4
Direct synthesis of fused 1,2,3,4,5-pentathiepins.
2005 Oct 7
A nonradioactive high-throughput/high-content assay for measurement of the human serotonin reuptake transporter function in vitro.
2006 Dec
Glyoxalase I-type hemithioacetal isomerization reactivity of a mononuclear Ni(II) deprotonated amide complex.
2006 Dec 27
EPR studies of amine radical cations. Part 2. Thermal and photo-induced rearrangements of propargylamine and allylamine radical cations in low-temperature freon matrices.
2006 Dec 28
Influence of endotoxin induced fever on the pharmacokinetics of intramuscularly administered cefepime in rabbits.
2006 Jun
Electrokinetic chromatographic characterization of novel pseudo-phases based on N-alkyl-N-methylpyrrolidinium ionic liquid type surfactants.
2006 Nov
Synthetic inhibitors of cytochrome P-450 2A6: inhibitory activity, difference spectra, mechanism of inhibition, and protein cocrystallization.
2006 Nov 30
Nicotine: on the potential role of ionic liquids for its processing and purification.
2007 Jul 19
1-Methyl-1-propyl-pyrrolidinium chloride.
2008 Feb 29
1,1'-Dimethyl-1,1'-(butane-1,4-di-yl)dipyrrolidinium dibromide methanol disolvate.
2008 Jan 11
Fiber diffraction as a screen for amyloid inhibitors.
2008 Jun
Rapid homogeneous lauroylation of wheat straw hemicelluloses under mild conditions.
2008 Nov 24
An improved ion chromatographic method for fast and sensitive determination of N-methylpyrrolidine in cefepime hydrochloride.
2009 Aug
Embryotoxic potential of N-methyl-pyrrolidone (NMP) and three of its metabolites using the rat whole embryo culture system.
2009 Jun 1
A simple and rapid dispersive liquid-liquid microextraction method followed by GC-FID for determination of N-methylpyrrolidine in cefepime.
2010 Dec
Validation of capillary electrophoresis method for determination of N-methylpyrrolidine in cefepime for injection.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:47:24 GMT 2023
Edited
by admin
on Fri Dec 15 17:47:24 GMT 2023
Record UNII
06509TZU6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-METHYLPYRROLIDINE
Systematic Name English
CEFEPIME IMPURITY G [EP IMPURITY]
Common Name English
PYRROLIDINE, 1-METHYL-
Systematic Name English
N-METHYLTETRAHYDROPYRROLE
Systematic Name English
NSC-65579
Code English
N-METHYLPYRROLIDINE
Systematic Name English
METHYLPYRROLIDINE, 1-
Systematic Name English
NSC-65
Code English
CEFEPIME DIHYDROCHLORIDE MONOHYDRATE IMPURITY G [EP IMPURITY]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-438-5
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID8042210
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
PUBCHEM
8454
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
NSC
65
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
CAS
120-94-5
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
FDA UNII
06509TZU6C
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
NSC
65579
Created by admin on Fri Dec 15 17:47:24 GMT 2023 , Edited by admin on Fri Dec 15 17:47:24 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE INACTIVE
Converted rapidly to NMP-N-oxide
MINOR
URINE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP