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[2-[3,4-dioctadecanoyloxy-2,5-bis(octadecanoyloxymethyl)oxolan-2-yl]oxy-3,5-dioctadecanoyloxy-6-(octadecanoyloxymethyl)oxan-4-yl] octadecanoate is a complex ester compound, characterized by its long-chain fatty acid structure derived from octadecanoic acid and related derivatives. This high molecular weight lipid is integral to the composition of biological membranes, where it contributes to the maintenance of membrane integrity and functionality. Its unique properties also make it a candidate for applications in pharmaceuticals and cosmetics, particularly due to its skin penetration capabilities and emollient effects.

34816-22-3

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34816-22-3 Usage

Uses

Used in Pharmaceutical Industry:
[2-[3,4-dioctadecanoyloxy-2,5-bis(octadecanoyloxymethyl)oxolan-2-yl]oxy-3,5-dioctadecanoyloxy-6-(octadecanoyloxymethyl)oxan-4-yl] octadecanoate is used as a pharmaceutical agent for its ability to penetrate the skin, which can enhance the delivery of drugs and improve their bioavailability. This property is particularly beneficial for transdermal drug administration, where the compound aids in the efficient transport of therapeutic agents across the skin barrier.
Used in Cosmetic Industry:
In the cosmetic industry, [2-[3,4-dioctadecanoyloxy-2,5-bis(octadecanoyloxymethyl)oxolan-2-yl]oxy-3,5-dioctadecanoyloxy-6-(octadecanoyloxymethyl)oxan-4-yl] octadecanoate is utilized as an emollient, providing a smooth and soft texture to the skin. Its capacity to moisturize and nourish the skin makes it a valuable ingredient in various cosmetic products, such as creams, lotions, and other skincare formulations, enhancing their efficacy in maintaining skin health and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 34816-22-3 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 34816-22:
(7*3)+(6*4)+(5*8)+(4*1)+(3*6)+(2*2)+(1*2)=113
113 % 10 = 3
So 34816-22-3 is a valid CAS Registry Number.

34816-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3R,4S,5R,6R)-6-[(2S,3S,4R,5R)-3,4-di(octadecanoyloxy)-2,5-bis(octadecanoyloxymethyl)oxolan-2-yl]oxy-3,4,5-tri(octadecanoyloxy)oxan-2-yl]methyl octadecanoate

1.2 Other means of identification

Product number -
Other names Thiourea,(1,4,5,6-tetrahydro-2-pyrimidinyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34816-22-3 SDS

34816-22-3Downstream Products

34816-22-3Relevant academic research and scientific papers

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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