Molecular Depot Biotinyl Hexylamine (Highly Pure) B2012873

Biotinyl Hexylamine (Highly Pure) is a high quality synthetic intermediate used in the synthesis of avidin nucleic acid nano assemblies. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Biotinyl Hexylamine (Highly Pure)
Catalog number:B2012873
Lot number:Batch Dependent
Expiration Date:Batch dependent
Amount:5 mg
Molecular Weight or Concentration:342.5 g/mol
Supplied as:Lyophilized Powder
Applications:molecular tool for various biochemical applications
Storage:-20°C
Keywords:(3aS,4S,6aR)-N-(6-aminohexyl)hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanamide
Grade:Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Food Safety Commission of Japan. Isobutylamine, Isopropylamine, sec-Butylamine, Propylamine, Hexylamine, Pentylamine and 2-Methylbutylamine (Flavoring Substances) Food Saf (Tokyo). 2019 Jun 28;7(2):54-55.
2: Jacob S, Delatouche B, Péré D, Ullah Khan Z, Ledoux MJ, Crispin X, Chmielowski R. High-performance flexible thermoelectric modules based on high crystal quality printed TiS(2)/hexylamine Sci Technol Adv Mater. 2021 Nov 24;22(1):907-916.
3: Kwon H, Etz BD, Montgomery MJ, Messerly R, Shabnam S, Vyas S, van Duin ACT, McEnally CS, Pfefferle LD, Kim S, Xuan Y. Reactive Molecular Dynamics Simulations and Quantum Chemistry Calculations To Investigate Soot-Relevant Reaction Pathways for Hexylamine Isomers J Phys Chem A. 2020 May 28;124(21):4290-4304.
4: Feldmann V, Engelmann J, Gottschalk S, Mayer HA. Synthesis, characterization and examination of Gd[DO3A-hexylamine]-functionalized silica nanoparticles as contrast agent for MRI-applications J Colloid Interface Sci. 2012 Jan 15;366(1):70-79.
5: Rocher NM, Frech R, Khan M. Hydrogen bonding and the inductive effect in crystalline and solution phases of hexylamine:LiCF3SO3 and Dipropylamine:LiCF3SO3: application to branched poly(ethylenimine) J Phys Chem B. 2005 Nov 10;109(44):20697-706.
6: Tsubaki K, Otsubo T, Morimoto T, Maruoka H, Furukawa M, Momose Y, Shang M, Fuji K. Modification of the upper rim of homooxacalix3arenes and complexation between a nitrohomooxacalix3arene derivative and n-hexylamine J Org Chem. 2002 Nov 15;67(23):8151-6.
7: Wei S, Peng J, Wang M, Fang X, Fan Y, Li X, Lu J. The (Zn(0.95)Mn(0.05)S)2·L (L = hexylamine and octylamine) inorganic/organic hybrid luminescence films by a spin-coating method Chem Commun (Camb). 2012 May 14;48(38):4615-7.
8: Donoso J, Muñoz F, García Del Vado A, Echevarría G, García Blanco F. Study of the hydrolysis and ionization constants of Schiff base from pyridoxal 5′-phosphate and n-hexylamine in partially aqueous solvents. An application to phosphorylase b Biochem J. 1986 Aug 15;238(1):137-44.
9: Rönquist-Nii Y, Eksborg S, Axelson M, Harmenberg J, Ekman S, Bergqvist M, Beck O. Determination of picropodophyllin and its isomer podophyllotoxin in human serum samples with electrospray ionization of hexylamine adducts by liquid chromatography-tandem mass spectrometry J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Feb 15;879(5-6):326-34.
10: Vázquez Segura MA, Donoso J, Muñoz F, García Blanco F, García del Vado MA, Echevarría G. Photophysical study of the Schiff bases of 5′-deoxypyridoxal and n-hexylamine in cationic micelles Photochem Photobiol. 1994 Nov;60(5):399-404.

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