78617-12-6 Usage
Description
HEPTYL-BETA-D-GLUCOPYRANOSIDE is a non-ionic surfactant and a glycoside derivative, which is composed of a heptyl chain attached to a beta-D-glucopyranose moiety. It is known for its ability to form micelles in aqueous solutions and has unique properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
HEPTYL-BETA-D-GLUCOPYRANOSIDE is used as a solubilizing agent for enhancing the solubility of membrane-bound proteins and hydrophobic drugs. Its amphiphilic nature allows it to interact with both hydrophilic and hydrophobic regions of proteins and drug molecules, improving their solubility and bioavailability.
Used in Cosmetic Industry:
HEPTYL-BETA-D-GLUCOPYRANOSIDE is used as an emulsifier and surfactant in cosmetic formulations. It helps to stabilize emulsions and create a uniform texture in products such as creams, lotions, and gels. Its mild and non-irritating properties make it suitable for use in personal care products.
Used in Research and Diagnostics:
HEPTYL-BETA-D-GLUCOPYRANOSIDE is used for lipid vesicle preparation, which is essential for studying the structure and function of biological membranes. Lipid vesicles are also used as model systems to investigate membrane-associated processes, such as protein-lipid interactions and membrane transport.
Used in Nanotechnology:
HEPTYL-BETA-D-GLUCOPYRANOSIDE is used in the development of nanocarriers for drug delivery systems. Its ability to form micelles and interact with hydrophobic molecules makes it a promising candidate for encapsulating and delivering drugs to specific target sites in the body, improving therapeutic efficacy and reducing side effects.
Purification Methods
Purify the glucoside by repeated crystallisation from Me2CO which is a better solvent than EtOAc. The acetate has m 66-68.5o and [] 20D -20.5o (c 4, CHCl3) [Pigman & Richtmyer J Am Chem Soc 64 369 1942]. [Beilstein 17 IV 2936.]
Check Digit Verification of cas no
The CAS Registry Mumber 78617-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,1 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78617-12:
(7*7)+(6*8)+(5*6)+(4*1)+(3*7)+(2*1)+(1*2)=156
156 % 10 = 6
So 78617-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O6/c1-2-3-4-5-6-7-18-13-12(17)11(16)10(15)9(8-14)19-13/h9-17H,2-8H2,1H3/t9-,10-,11+,12-,13-/m1/s1
78617-12-6Relevant articles and documents
Highly β-Selective Glycosylation Reactions for the Synthesis of ω-Functionalized Alkyl β-Maltoside as a Co-crystallizing Detergent
Elias, M.,Hossain, M. A.,Jamil, M. A. R.,Rahman, M. M.,Siddiki, S. M. A. Hakim
, p. 1806 - 1814 (2020/12/01)
Abstract: Methods have been reported for the preparation of ω-functionalized alkyl maltoside and glycoside detergents via a simple and inexpensive synthetic route. The key step was stannic chloride-mediated glycosylation of long-chain alcohols or thiols with maltose octaacetate at 0 or –10°C, respectively, within a very short time (isolated yield 17–44%), which provided more than 98% β-selectivity.
Significantly improved equilibrium yield of long-chain alkyl glucosides via reverse hydrolysis in a water-poor system using cross-linked almond meal as a cheap and robust biocatalyst
Wang, Qinqqin,Yu, Huilei,Zhao, Na,Li, Chunxiu,Shang, Yazhuo,Liu, Honglai,Xu, Jianhe
, p. 275 - 280 (2012/06/29)
An array of ten β-D-glucopyranosides with varied alkyl chain lengths were enzymatically synthesized. It was found that for longer alkyl chains a lower initial rate and final yield of glucoside was obtained except for methyl glucoside because of the severe toxicity of methanol to the enzyme. From a thermodynamics point of view, the equilibrium constant and Gibbs free energy variation of the glucoside syntheses were systematically investigated. To improve the final yields of the glucosides containing long alkyl chains the equilibrium of the enzymatic glucoside synthesis was altered. The equilibrium yield of decyl β-D-glucoside increased from 1.9 to 6.1 when the water content was reduced from 10 to 5 (v/v) using tert-butanol as a cosolvent and 0.10 mol/L of glucose as a substrate. As for the other longer alkyl chain glucosides, heptyl β-D-glucoside was found to have significant surface activity as well.
POLYMER STABILIZER
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, (2010/08/03)
A polymer stabilizer comprising the following alkoxy compound: the alkoxy compound: a compound obtained by alkoxylating at least one hydroxyl group contained in a compound of the following formula (1) containing one formyl group or carbonyl group and (n?1) hydroxyl groups in the molecule with an alkyl group having 1 to 12 carbon atoms: [in-line-formulae]CnH2nOn??(1)[/in-line-formulae] (wherein, n represents an integer of 3 or more).