Hexanoic acid,6-[[6-[[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]amino]-1-oxohexyl]amino]-


Chemical Name: Hexanoic acid,6-[[6-[[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]amino]-1-oxohexyl]amino]-
CAS Number: 89889-51-0
Product Number: AG00GWQL(AGN-PC-0VPR0W)
Synonyms:
MDL No:
Molecular Formula: C22H38N4O5S
Molecular Weight: 470.62592

Identification/Properties


Properties
MP:
185-195°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
470.629g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
17
Exact Mass:
470.256g/mol
Monoisotopic Mass:
470.256g/mol
Topological Polar Surface Area:
162A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
633
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



N-Biotinylcaproylaminocaproic acid, also known as Biotin-6-Aminohexanoic Acid N-Hydroxysuccinimide Ester, plays a crucial role in chemical synthesis as a versatile and highly efficient reagent. This compound is widely utilized in bioconjugation and protein chemistry as a key component for the modification and functionalization of biomolecules. Its ability to selectively attach biotin to specific sites on proteins or nucleic acids makes it an essential tool in various research and diagnostic applications. Furthermore, N-Biotinylcaproylaminocaproic acid exhibits remarkable stability and compatibility with a wide range of solvents, making it a preferred choice for conjugation reactions in aqueous and organic environments. Its precise and controlled reactivity allows for the seamless creation of biotinylated molecules with enhanced affinity for avidin/streptavidin-based detection systems in immunoassays, protein purification, and targeted drug delivery. Beyond its applications in biotechnology, N-Biotinylcaproylaminocaproic acid serves as a valuable building block in the synthesis of specialized materials, pharmaceuticals, and research tools, enabling advancements in diverse fields such as molecular biology, drug development, and nanotechnology.