Weight | 92.094 g/mol |
---|---|
Formula | C3H8O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Glycerol
Glycerin · Glycerine · 1,2,3-Trihydroxypropane
8013-25-0, 56-81-5, 25618-55-7, 8043-29-6
Score:
#49 in Physics
,
#103 in Biology
,
#105 in Chemistry
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- Dielectric Relaxation in Glycerol, Propylene Glycol, and nPropanol (Journal of Chemical Physics, 1951)
- Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals (Chemical Society Reviews, 2008)
- From Glycerol to Value-Added Products (Angewandte Chemie, 2007)
- Mechanism of protein stabilization by glycerol: preferential hydration in glycerol water mixtures. (Biochemistry, 1981)
- Improved utilisation of renewable resources: New important derivatives of glycerol (Green Chemistry, 2008)
- Structure and Mechanism of the Glycerol-3-Phosphate Transporter from Escherichia Coli (Science, 2003)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Glycerin
- Glycerine
- 1,2,3-Trihydroxypropane
-
SMILESC(C(CO)O)O
-
InChIKeyPEDCQBHIVMGVHV-UHFFFAOYSA-N
- Pubchem - Glycerol
- Wikipedia - glycerin
Glycerol (; also called glycerine or glycerin; see spelling differences) is a simple polyol compound. It is a colorless, odorless, viscous liquid that is sweet-tasting and non-toxic. The glycerol backbone is found in all lipids known as triglycerides.
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Estimated Properties
Boiling Point | 258.88 C | EPA T.E.S.T. |
---|---|---|
Density | 1.2 g/cm3 | EPA T.E.S.T. |
Flash Point | 133.45 C | EPA T.E.S.T. |
Water Solubility | 499599 mg/L | EPA T.E.S.T. |
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