1083-56-3 Purity
96%
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Specification
Diethylene glycol distearate (DGD) was used as a removable embedding medium to generate embedding-free sections for transmission electron microscopy. DGD embedded materials offer several significant advantages, including (a) being greatly reduced in brittleness so that they do not crack and shatter when the block is cut, (b) the slices can float on a water-filled trough, and slice strips can be produced , and (c) the section will produce an interference color or allow the selection of sections of equal thickness. The embedding medium is then removed without causing significant damage to the biological material.
Cell preparation and embedding in DGD
· MDCK cells were grown on glass culture dishes and processed in situ by extraction, fixation, and embedding.
· Cells were immersed in 2:1 and 1:2 n-butanol (nBA)/ethanol mixtures followed by four changes of nBA for 15 min each.
· Since DGD is solid at room temperature, it was kept at 60°C to remain molten during the investment process.
· Cells were transferred from 100% nBA to DGD via a series of 2:1 and then 1:2 nBA/DGD mixtures at 60°C for 10 min each, followed by 3 changes of 100% DGD for 1 h each.
· Remove the cells mounted on the glass Petri dish from the oven and allow the DGD to harden.
Diethylene glycol distearate is a valuable tool for electron microscopy studies, as it can improve the quality of imaging and provide researchers with clear, detailed images of biological samples. In a work to study the structure and developmental dynamics of matrix-related regions of the Drosophila genome, nuclear matrix (NuMat) samples were prepared and embedded in diethylene glycol distearate (DGD) for electron microscopy analysis.
Electron microscopy of NuMat samples in DGD
· For embedment free electron microscopy (EM), after dehydrating the samples, they were suspended in a mixture of butanol and ethanol (1:2) at room temperature for 15 minutes. This process was repeated with different ratios of butanol to ethanol (2:1) until reaching 100% butanol.
· Subsequently, the samples were embedded in DGD by gradually transitioning them from butanol to DGD with increasing concentrations of DGD and 15-minute incubations at 60°C at each stage.
· Finally, the samples were incubated at 60°C with 100% DGD for 1 hour. The blocks were cooled, trimmed, and sectioned using an ultramicrotome with a glass knife set at a 10° angle.
· The sections were placed on poly-L-lysine coated copper grids and dried. The DGD was removed from the sections and then dried using CO2 critical point drying.
The molecular formula of diethylene glycol distearate is C40H78O5.
Some synonyms of diethylene glycol distearate are Witconol CAD and Oxydiethylene stearate.
The molecular weight of diethylene glycol distearate is 639.0 g/mol.
Diethylene glycol distearate was created on March 27, 2005.
Diethylene glycol distearate was last modified on October 21, 2023.
The IUPAC name of diethylene glycol distearate is 2-(2-octadecanoyloxyethoxy)ethyl octadecanoate.
The InChI of diethylene glycol distearate is InChI=1S/C40H78O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-39(41)44-37-35-43-36-38-45-40(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-38H2,1-2H3.
The InChIKey of diethylene glycol distearate is YKDMBTQVKVEMSA-UHFFFAOYSA-N.
The Canonical SMILES of diethylene glycol distearate is CCCCCCCCCCCCCCCCC(=O)OCCOCCOC(=O)CCCCCCCCCCCCCCCC.
The CAS number of diethylene glycol distearate is 109-30-8.