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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

b-D-Glucopyranoside, nonyl

CCCCCCCCCO[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O Request for Quotation
Chemical Name: b-D-Glucopyranoside, nonyl
CAS Number: 69984-73-2
Product Number: AG00IBZZ(AGN-PC-0TXGKY)
Synonyms:
MDL No:
Molecular Formula: C15H30O6
Molecular Weight: 306.3951

Identification/Properties

Computed Properties
Molecular Weight:
306.399g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
10
Exact Mass:
306.204g/mol
Monoisotopic Mass:
306.204g/mol
Topological Polar Surface Area:
99.4A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
263
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Nonyl β-D-glucopyranoside is a versatile chemical compound commonly used in chemical synthesis as a non-ionic detergent and mild surfactant. Its unique structure and properties make it valuable in various applications within the field of chemistry.In chemical synthesis, Nonyl β-D-glucopyranoside serves as a non-denaturing detergent, facilitating the solubilization and stabilization of proteins and membrane-bound receptors. This attribute is crucial in the structural and functional studies of biomolecules, as it helps maintain the native conformation and activity of the biomolecular target during purification and analysis processes.Additionally, Nonyl β-D-glucopyranoside is employed in the preparation of liposomal formulations for drug delivery systems. By acting as a surfactant, it aids in the encapsulation of hydrophobic drugs within liposomes, enhancing their stability and bioavailability. This application is particularly important in the pharmaceutical industry for developing effective and targeted drug delivery strategies.Furthermore, Nonyl β-D-glucopyranoside is utilized in the synthesis of glycosylated compounds and glycolipids, owing to its glycosidic nature. Its ability to serve as a glycosyl donor in chemical reactions enables the functionalization of various molecules with sugar moieties, leading to the production of diverse glycoconjugates with potential biological activities.Overall, the role of Nonyl β-D-glucopyranoside in chemical synthesis extends to protein research, drug delivery systems, and the synthesis of bioactive compounds, highlighting its significance in advancing scientific discoveries and innovative applications in the field of chemistry.