Molecular structure of 1,7-Diaminoheptane, CAS Number: 646-19-5
1,7-Diaminoheptane (CAS 646-19-5)
CAS Number:
646-19-5
Purity:
98%
Molecular Weight:
130.23
Molecular Formula:
C7H18N2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
1,7-Diaminoheptane is a redox potential molecule shown to react with other compounds to form a diazonium salt. It has been used in the synthesis of amines, and as an intermediate in the preparation of NMR spectra. Also used in preparation of semi-aromatic copolymerized polyamide.
1,7-Diaminoheptane (CAS 646-19-5) References
- Urine polyamines determination using dansyl chloride derivatization in solid-phase extraction cartridges and HPLC. | Molins-Legua, C., et al. 1999. Analyst. 124: 477-82. PMID: 10605877
- Effect of drugs inhibiting spermidine biosynthesis and metabolism on the in vitro development of Plasmodium falciparum. | Kaiser, A., et al. 2001. Parasitol Res. 87: 963-72. PMID: 11728024
- 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. | Loukou, Z. and Zotou, A. 2003. J Chromatogr A. 996: 103-13. PMID: 12830912
- Haemolytic action of N-alkylpolymethylenediamines. | Miyamoto, E., et al. 1992. J Pharm Pharmacol. 44: 269-71. PMID: 1354739
- Separation of low-molecular mass peptides by capillary electrophoresis with the use of alkylamines as dynamic coating agents at low pH. | Eckhardt, A., et al. 2004. J Chromatogr A. 1051: 111-7. PMID: 15532562
- Behavior and characteristics of biogenic amines, ornithine and lysine derivatized with the o-phthalaldehyde-ethanethiol-fluorenylmethyl chloroformate reagent. | Hanczko, R., et al. 2005. J Chromatogr A. 1087: 210-22. PMID: 16130716
- 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. | Korös, A., et al. 2007. J Chromatogr A. 1149: 46-55. PMID: 17145062
- Synthesis and structure of a new heptaborate oxoanion isomer: B7O9(OH)5(2-). | Schubert, DM., et al. 2008. Inorg Chem. 47: 4740-5. PMID: 18416525
- Water-induced folding of 1,7-diammoniumheptane. | Demireva, M., et al. 2012. J Am Chem Soc. 134: 11216-24. PMID: 22708846
- A label-free impedimetric immunosensor for direct determination of the textile dye Disperse Orange 1. | Yang, J., et al. 2015. Talanta. 142: 183-9. PMID: 26003710
- Environmentally friendly solid-phase microextraction coupled with gas chromatography and mass spectrometry for the determination of biogenic amines in fish samples. | Huang, J., et al. 2016. J Sep Sci. 39: 4384-4390. PMID: 27753266
- Polyamines control human chorionic gonadotropin production in the JEG-3 choriocarcinoma cell. | Moore, JJ., et al. 1988. J Biol Chem. 263: 12765-9. PMID: 2842342
- Liquid Chromatographic Determination of Biogenic Amines in Fish Based on Pyrene Sulfonyl Chloride Pre-Column Derivatization. | Plakidi, ES., et al. 2020. Foods. 9: PMID: 32397518
- Differential effect of alpha-difluoromethylornithine on the in vivo uptake of 14C-labeled polyamines and methylglyoxal bis(guanylhydrazone) by a rat prostate-derived tumor. | Heston, WD., et al. 1984. Cancer Res. 44: 1034-40. PMID: 6420052
- Branched-chain and unsaturated 1,7-diaminoheptane derivatives as deoxyhypusine synthase inhibitors. | Lee, YB. and Folk, JE. 1998. Bioorg Med Chem. 6: 253-70. PMID: 9568280
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,7-Diaminoheptane, 5 g | sc-237793 | 5 g | $38.00 |