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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)-

D-Glucopyranoside, decyl

CCCCCCCCCCOC1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O Request for Quotation
Chemical Name: D-Glucopyranoside, decyl
CAS Number: 54549-25-6
Product Number: AG00DLKA(AGN-PC-0OC385)
Synonyms:
MDL No:
Molecular Formula: C16H32O6
Molecular Weight: 320.42168

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Chemical Structure


Decyl D-glucopyranoside is a versatile nonionic surfactant commonly used in chemical synthesis as a mild and environmentally friendly detergent. Its unique properties make it a valuable reagent in various chemical reactions, particularly in organic synthesis and separation processes. Due to its low toxicity and biodegradability, Decyl D-glucopyranoside is favored in green chemistry practices. Its ability to lower surface tension and enhance solubility makes it ideal for emulsification and dispersion of hydrophobic compounds in aqueous solutions. Additionally, Decyl D-glucopyranoside is known for its compatibility with a wide range of chemical compounds, making it a popular choice for facilitating reactions in both academic and industrial settings. By acting as a surfactant and solubilizing agent, Decyl D-glucopyranoside plays a crucial role in promoting efficient and sustainable chemical synthesis methods.