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Details

Stereochemistry RACEMIC
Molecular Formula C3H7N
Molecular Weight 57.0944
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPYLENIMINE

SMILES

CC1CN1

InChI

InChIKey=OZDGMOYKSFPLSE-UHFFFAOYSA-N
InChI=1S/C3H7N/c1-3-2-4-3/h3-4H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C3H7N
Molecular Weight 57.0944
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Renal toxicity of propyleneimine: assessment by non-invasive techniques in the rat.
1986 Oct
Investigations into the biochemical effects of region-specific nephrotoxins.
1989 Feb
1H NMR spectroscopic and histopathological studies on propyleneimine-induced renal papillary necrosis in the rat and the multimammate desert mouse (Mastomys natalensis).
1997 Feb
Cu(0) nanoclusters derived from poly(propylene imine) dendrimer complexes of Cu(II).
2001 Oct 31
2-Methylaziridine (propylenimine).
2002
Mechanism of charging and supercharging molecules in electrospray ionization.
2003 Feb 26
Synthesis of thermoresponsive polyurethane from 2-methylaziridine and supercritical carbon dioxide.
2004 Jan 30
Substituent effects on the ring opening of 2-aziridinylmethyl radicals.
2005 Apr 29
Lipoplexes based on cholesterol derivatives of oligo (ethylene propylene imines) in gene transfer in vitro and in vivo.
2005 Mar-Apr
Double stimuli-responsive behavior of aliphatic poly(urethane-amine)s derived from supercritical carbon dioxide.
2005 May 7
The influence of densely organized maltose shells on the biological properties of poly(propylene imine) dendrimers: new effects dependent on hydrogen bonding.
2008
Progress in antiretroviral drug delivery using nanotechnology.
2010 Aug 9
Ring-opening reactions within porous metal-organic frameworks.
2010 Jul 19
Influence of surface functionality of poly(propylene imine) dendrimers on protease resistance and propagation of the scrapie prion protein.
2010 May 10
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:40:24 GMT 2023
Edited
by admin
on Sat Dec 16 05:40:24 GMT 2023
Record UNII
ULC972Q7TZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROPYLENIMINE
Common Name English
2-METHYLAZIRIDINE [IARC]
Common Name English
DL-2-METHYLAZIRIDINE
Common Name English
NSC-20655
Code English
AZIRIDINE, 2-METHYL-
Systematic Name English
PROPYLENEIMINE
HSDB  
Common Name English
PROPYLENEIMINE [HSDB]
Common Name English
2-METHYLAZIRIDINE
Systematic Name English
2-METHYLAZIRIDINE, (±)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C45176
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
Code System Code Type Description
MESH
C031132
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
NSC
20655
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID8024286
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
HSDB
739
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
FDA UNII
ULC972Q7TZ
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
NCI_THESAURUS
C44439
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
PUBCHEM
6377
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
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WIKIPEDIA
PROPYLENEIMINE
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-878-7
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY
CAS
75-55-8
Created by admin on Sat Dec 16 05:40:24 GMT 2023 , Edited by admin on Sat Dec 16 05:40:24 GMT 2023
PRIMARY