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Details

Stereochemistry ACHIRAL
Molecular Formula C5H14N2
Molecular Weight 102.1781
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-DIMETHYLAMINOPROPYLAMINE

SMILES

CN(C)CCCN

InChI

InChIKey=IUNMPGNGSSIWFP-UHFFFAOYSA-N
InChI=1S/C5H14N2/c1-7(2)5-3-4-6/h3-6H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C5H14N2
Molecular Weight 102.1781
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chromosome targeting at short polypurine sites by cationic triplex-forming oligonucleotides.
2001 Oct 19
NMR characterization of the DNA binding properties of a novel Hoechst 33258 analogue peptide building block.
2002 Sep-Oct
The role of 3-dimethylaminopropylamine and amidoamine in contact allergy to cocamidopropylbetaine.
2003 Apr
Migration of methyl groups between aliphatic amines in water.
2003 Jan 15
[Functionalization of oligonucleotides containing internucleotide phosphoamide bonds].
2003 Jan-Feb
Allergic contact dermatitis from cocamidopropyl betaine, cocamidoamine, 3-(dimethylamino)propylamine, and oleamidopropyl dimethylamine: co-reactions or cross-reactions?
2004 Sep
Synthesis and characterization of a trifunctional aminoamide cellulose derivative.
2006 Jan
An efficient vector for gene delivery: alpha,beta-poly (3-dimethylaminopropyl-D,L-aspartamide).
2007 Jun
Amended final report of the safety assessment of cocamidopropylamine oxide.
2008
A study of the sensitization rate to cocamidopropyl betaine in patients patch tested in a university hospital of Beijing.
2008 Jan
Dichlorido[3-dimethyl-amino-N-(2-pyridylmethyl-ene)propyl-amine-κN,N',N'']cadmium(II).
2008 Nov 8
Eyelid dermatitis: contact allergy to 3-(dimethylamino)propylamine.
2008 Nov-Dec
DNA interaction with PtCl2(LL) (LL = chelating diamine ligand: N,N-dimethyltrimethylendiamine) complex.
2009 Jul
A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells.
2010 Sep
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:14:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:14:20 GMT 2023
Record UNII
I98I2UEC03
Record Status Validated (UNII)
Record Version
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Name Type Language
3-DIMETHYLAMINOPROPYLAMINE
Systematic Name English
DIMETHYLAMINOPROPYLAMINE
Systematic Name English
3-(DIMETHYLAMINO)PROPYLAMINE
Systematic Name English
3-AMINOPROPYLDIMETHYLAMINE
Systematic Name English
1,3-PROPANEDIAMINE, N,N-DIMETHYL-
Systematic Name English
NSC-1067
Code English
.GAMMA.-(DIMETHYLAMINO)PROPYLAMINE
Systematic Name English
DIMETHYLAMINOPROPYLAMINE [INCI]
Common Name English
N,N-DIMETHYL-1,3-PROPANEDIAMINE [HSDB]
Common Name English
Code System Code Type Description
FDA UNII
I98I2UEC03
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
CAS
109-55-7
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
WIKIPEDIA
Dimethylaminopropylamine
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
DAILYMED
I98I2UEC03
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
HSDB
5391
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
PUBCHEM
7993
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
NSC
1067
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-680-9
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID5025102
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY
RXCUI
1661327
Created by admin on Fri Dec 15 19:14:20 GMT 2023 , Edited by admin on Fri Dec 15 19:14:20 GMT 2023
PRIMARY RxNorm