72040-64-3

72040-64-3 structure

Name: N-Biotinyl-6-aminohexanoic acid
Chemical Name: N-Biotinylcaproic Acid
CAS Number: 72040-64-3
Molecular Formula: C₁₆H₂₇N₃O₄S
Molecular Weight: 357.46800
Catalog: Research Areas Others
Create Date: 2018-04-10 08:00:00
Modify Date: 2024-01-07 17:10:35
N-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation[1].

Name	N-Biotinylcaproic Acid
Synonyms	6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]hexanoic acid

Description	N-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
In Vitro	Synthesis of p-nitrophenyl N-acetyllactosaminide with β-D-galactosidase, chemical reduction of the p-nitrophenyl group, and sialylation with sialyltransferase. The p-aminophenyl glycosides are then successfully biotin-labeled through the coupling with N-(+)-biotinyl-6- aminohexanoic acid to afford biotinylated oligosaccharides with an aminohexanosyl group and phenyl group as the spacers between the biotin and glycan[1]. The SERS (surface-enhanced Raman scattering) of cyclohexyl isocyanide that silver nanoparticles modified with N-(+)-biotinyl-6-aminocaproic acid and cyclohexyl isocyanide can be anchored on a separate biotinylated substrate via the avidin-biotin interaction[2].
References	[1]. Zeng X, et al. Effective chemoenzymatic synthesis of p-aminophenyl glycosides of sialyl N-acetyllactosaminide and analysis of their interactions with lectins. Carbohydr Res. 2007 Jul 2;342(9):1244-8. [2]. Kim K, et al. microAg particle-based molecular sensing/recognition via surface-enhanced Raman spectroscopy. Biosens Bioelectron. 2007 Jan 15;22(6):1000-5.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	F: Flammable;
Safety Phrases	22-24/25
RIDADR	NONH for all modes of transport

58-85-5

60-32-2

~76%

72040-64-3

35013-72-0

60-32-2

~79%

72040-64-3

Literature: Shi, Haibin; Liu, Kai; Xu, Ashley; Yao, Shao Q. Chemical Communications, 2009 , # 33 p. 5030 - 5032

1306616-52-3

60-32-2

72040-64-3

Literature: US2012/232262 A1, ; Page/Page column 3 ;

58-85-5

72040-64-3

Literature: US2012/232262 A1, ;

120550-35-8

72040-64-3

Literature: Journal of Labelled Compounds and Radiopharmaceuticals, , vol. 43, # 4 p. 309 - 322

1926-80-3

72040-64-3

Literature: Journal of Labelled Compounds and Radiopharmaceuticals, , vol. 43, # 4 p. 309 - 322