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Details

Stereochemistry ACHIRAL
Molecular Formula C7H18N2
Molecular Weight 130.2312
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEPTAMETHYLENEDIAMINE

SMILES

NCCCCCCCN

InChI

InChIKey=PWSKHLMYTZNYKO-UHFFFAOYSA-N
InChI=1S/C7H18N2/c8-6-4-2-1-3-5-7-9/h1-9H2

HIDE SMILES / InChI

Molecular Formula C7H18N2
Molecular Weight 130.2312
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dimeric versus polymeric coordination in copper(II) cationic complexes with bis(chelating) oxime and amide ligands.
2010-07-21
Plasmodium falciparum spermidine synthase inhibition results in unique perturbation-specific effects observed on transcript, protein and metabolite levels.
2010-04-12
Simultaneous determination of different polyamines and their mono-acetylated derivatives in gastric tissue by HPLC with post-column derivatization.
2010-01-05
Protein and metabolite analysis reveals permanent induction of stress defense and cell regeneration processes in a tobacco cell suspension culture.
2009-07-06
Underivatized polyamine analysis in plant samples by ion pair LC coupled with electrospray tandem mass spectrometry.
2009-07
The role of polyamines in protein-dependent hypoxic tolerance of Drosophila.
2008-12-02
Synthesis and structure of a new heptaborate oxoanion isomer: B7O9(OH)5(2-).
2008-06-02
Analysis of amino acids and biogenic amines in biological tissues as their o-phthalaldehyde/ethanethiol/fluorenylmethyl chloroformate derivatives by high-performance liquid chromatography. A deproteinization study.
2007-05-11
Evaluation of two different extraction methods for chromatographic determination of bioactive amines in tomato products.
2006-05-15
Behavior and characteristics of biogenic amines, ornithine and lysine derivatized with the o-phthalaldehyde-ethanethiol-fluorenylmethyl chloroformate reagent.
2005-09-16
[Method of determination of biogenic amines in wines by high-performance liquid chromatography with fluorescence detector and ultraviolet detector].
2005-09
Synthesis and characterization of fluorescent poly(aromatic amide) dendrimers.
2005-01-07
Separation of low-molecular mass peptides by capillary electrophoresis with the use of alkylamines as dynamic coating agents at low pH.
2004-10-08
The efficacy of inhibitors involved in spermidine metabolism in Plasmodium falciparum, Anopheles stephensi and Trypanosoma evansi.
2004-09
Simultaneous analysis of amino acid and biogenic polyamines by high-performance liquid chromatography after pre-column derivatization with N-(9-fluorenylmethoxycarbonyloxy)succinimide.
2004-02-06
Coordination chemistry of chromium-Salen complexes studied by electrospray ionization mass spectrometry.
2004
Equations of substrate-inhibition kinetics applied to pig kidney diamine oxidase (DAO, E.C. 1.4.3.6).
2003-12
[The effect of eIF-5A on the G1-S in cell cycle regulation].
2003-08
Proteomic analysis of ubiquitin-proteasome effects: insight into the function of eukaryotic initiation factor 5A.
2003-07-31
Determination of biogenic amines as dansyl derivatives in alcoholic beverages by high-performance liquid chromatography with fluorimetric detection and characterization of the dansylated amines by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry.
2003-05-09
Identification and quantification of amines in the equine caecum.
2003-04
Effect of drugs inhibiting spermidine biosynthesis and metabolism on the in vitro development of Plasmodium falciparum.
2001-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:59:15 GMT 2025
Edited
by admin
on Mon Mar 31 19:59:15 GMT 2025
Record UNII
3011L9B20C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-45777
Preferred Name English
HEPTAMETHYLENEDIAMINE
Systematic Name English
1,7-DIAMINO-N-HEPTANE
Common Name English
1,7-HEPTANEDIAMINE
Systematic Name English
Code System Code Type Description
NSC
45777
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
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FDA UNII
3011L9B20C
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
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CAS
646-19-5
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
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EPA CompTox
DTXSID60214848
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
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PUBCHEM
69533
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
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ECHA (EC/EINECS)
211-468-2
Created by admin on Mon Mar 31 19:59:15 GMT 2025 , Edited by admin on Mon Mar 31 19:59:15 GMT 2025
PRIMARY