| Identification | Back Directory | [Name]
glucosylglycerol | [CAS]
22160-26-5 | [Synonyms]
GG
Glycoin
Skycore AGG
Extremys GG
glucosylglycerol
glycosylglycerol
GLYCERYL GLUCOSIDE
2-O-α-D-Glucosylglycerol
glucosylglycerol USP/EP/BP
2-O-alpha-D-Glucosylglycerol
2-O-(α-D-glucopyranosyl)-glycerol
2-O-α-D-Glucosylglycerol:Glucosylglycerol:Extremys GG:Glycoin:GLYCERYL GLUCOSIDE | [EINECS(EC#)]
-0 | [Molecular Formula]
C9H18O8 | [MDL Number]
MFCD19980985 | [MOL File]
22160-26-5.mol | [Molecular Weight]
254.24 |
| Chemical Properties | Back Directory | [Melting point ]
121 °C | [Boiling point ]
606.1±55.0 °C(Predicted) | [density ]
1.58±0.1 g/cm3(Predicted) | [vapor pressure ]
0.022Pa | [storage temp. ]
Hygroscopic, Refrigerator, under inert atmosphere | [solubility ]
Methanol (Slightly), Water (Slightly, Sonicated) | [form ]
Solid | [pka]
12.85±0.70(Predicted) | [color ]
White to Off-White | [Stability:]
Very Hygroscopic | [Cosmetics Ingredients Functions]
HUMECTANT
SKIN CONDITIONING | [InChI]
InChI=1/C9H18O8/c10-1-4(2-11)16-9-8(15)7(14)6(13)5(3-12)17-9/h4-15H,1-3H2/t5-,6-,7+,8-,9+/s3 | [InChIKey]
AQTKXCPRNZDOJU-QHXZDXPMNA-N | [SMILES]
O([C@@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)C(CO)CO |&1:1,2,3,5,7,r| | [LogP]
-3.46 |
| Questions And Answer | Back Directory | [Structure]
According to the stereo conformation of glycosidic linkages, naturally occurring Glucosylglycerols (GGs) are generally divided into α-GGs and β-GGs. Whereas α-GGs are mainly identified in microorganisms during their responses to environmental stresses, to date, β-GGs are found exclusively in higher plants. |
| Hazard Information | Back Directory | [Description]
Glucosylglycerols (GGs) are a group of small heterosides comprising one molecule of glucose and one molecule of glycerol via glycosidic bonds. In nature, glycosidic linkages within GGs are established between the C1-hydroxyl group of glucose and one of the three hydroxyl groups of sn-glycerol. They are mainly produced by many moderately salt-tolerant cyanobacteria as compatible solutes in a salt-dependent manner and synthesized in a few higher plants and fermentation processes. Because of their many interesting physicochemical properties and biological activities, such as low sweetness, low hygroscopicity, high water-holding capacity, excellent biocompatibility, favourable performance in protecting macromolecules, and antitumor activity, GGs exhibit large application potential in the fields of cosmetics, health care, food service, enzyme production, and pharmaceuticals[1].
| [Uses]
2-O-α-D-Glucosylglycerol is used to prepare glycoglycerolipid analogs active as antitumor-promoters the influence of the anomeric configuration. | [Definition]
ChEBI: 2-O-(alpha-D-glucopyranosyl)glycerol is a glucosylglycerol consisting of an alpha-D-glucosyl residue attached at position 2 of glycerol via a glycosidic bond. It has a role as an osmolyte and a bacterial metabolite. It is a glucosylglycerol and an alpha-D-glucoside. | [Synthesis]
Glucosylglycerol is extracted and purified from microalgae culture. Steps include: 1) Harvesting and washing of microalgal cells. 2) Homogenization and primary dehydration of cells. 3) Three-stage counter-current extraction to obtain an extract containing | [References]
[1] Quan Luo, Xuefeng Lu, Yangkai Duan . “Biological sources, metabolism, and production of glucosylglycerols, a group of natural glucosides of biotechnological interest.” Biotechnology advances 59 (2022): Article 107964. |
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Beri Pharma Co., Ltd. Gold
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T&W GROUP
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Puripharm Co., Ltd.
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