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34816-23-4

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  • 1,3,4,6-Tetrakis-O-(1-oxo-9-octadecenyl)-beta-D-fructofuranosyl-alpha-D-glucopyranoside tetraoleate

    Cas No: 34816-23-4

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34816-23-4 Usage

Molecular structure

A complex chemical compound consisting of a fructose-derived molecule attached to four oleic acid molecules.

Category

Belongs to the category of saccharides and oleates.

Industry applications

Commonly used in the food and cosmetic industries.

Emollient properties

Known for its emollient and conditioning properties, making it a popular ingredient in moisturizing creams and lotions.

Emulsifier

Used as an emulsifier in food products, helping to stabilize and blend the different components of a mixture.

Versatility

A versatile compound with a variety of practical applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 34816-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,1 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34816-23:
(7*3)+(6*4)+(5*8)+(4*1)+(3*6)+(2*2)+(1*3)=114
114 % 10 = 4
So 34816-23-4 is a valid CAS Registry Number.

34816-23-4Downstream Products

34816-23-4Relevant articles and documents

Membrane perturbing properties of sucrose polyesters

McManus, Gerald G.,Buchanan, Gerald W.,Jarrell, Harold C.,Epand, Richard M.,Epand, Raquel F.,Cheetham, James J.

, p. 185 - 202 (2007/10/03)

Sucrose polyester (SPE), in the form of sucrose octaesters and sucrose hexaesters of palmitic (16:0), stearic (18:0), oleic (18:1cis), and linoleic (18:2cis) acids, have many uses. Applications include: A non-caloric fat substitute, detoxification agent, and oral contrast agent for human abdominal (MRI) magnetic resonance imaging. However, it has been shown that the ingestion of SPE was shown to generate a depletion of physiologically important lipidic vitamins and other lipophilic molecules. In order to better understand, at the molecular level, the type of interaction between SPE and lipid membrane, we have, first synthesized different type of labelled and non-labelled SPEs. Secondly, we have studied the effect of SPEs on multilamellar dispersions of dielaidoylphosphatidylethanolamine (DEPE) and dipalmitoylphosphocholine (DPPC) as a function of temperature, SPE composition and concentration. The effects of SPEs were studied by differential scanning calorimetry (DSC), X-ray diffraction, 2H and 31P NMR spectroscopy. At low concentration (a cubic phase in a composition dependent manner. At the same low concentration, SPEs in DPPC induce the formation of a non-bilayer phase as seen by 31P NMR. Order parameter measurements of DPPC-d62/SPE mixtures show that the SPE effect on the DPPC monolayer thickness is dependent on the SPE, concentration, chains length and saturation level. At higher concentration (≥10 mol%) SPE are very potent DEPE bilayer to HII phase transition promoters, although at that concentration the SPE have lost the ability to form cubic phases. SPEs have profound effects on the phase behaviour of model membrane systems, and may be important to consider when developing current and potential industrial and medical applications.

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