Weight | 218.205 g/mol |
---|---|
Formula | C9H14O6 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
triacetin (102-76-1)
Enzactin · Triacetyl glycerol · Triacetylglycerol
Score:
#992 in Biology
,
#1099 in Chemistry
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- Sigma-Aldrich - triacetin40.00 - 800.00 USD
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- TCI - triacetin14.00 - 23.00 USD
- Transesterification of triacetin with methanol on solid acid and base catalysts (Applied Catalysis A-general, 2005)
- Transesterification of triacetin with methanol on Nafion acid resins (Journal of Catalysis, 2007)
- Fast responses from slowly relaxing liquids: A comparative study of the femtosecond dynamics of triacetin, ethylene glycol, and water (Journal of Chemical Physics, 1993)
- Lipase kinetics: Hydrolysis of triacetin by lipase from Candida cylindracea in a hollowfiber membrane reactor (Biotechnology and Bioengineering, 1991)
- Transesterification of triacetin using solid Brnsted bases (Journal of Catalysis, 2007)
- Effects of Triacetin on Biodiesel Quality (Energy & Fuels, 2010)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Enzactin
- Triacetyl glycerol
- Triacetylglycerol
- Triacetyl-glycerol
-
SMILESCC(=O)OCC(COC(=O)C)OC(=O)C
-
InChIKeyURAYPUMNDPQOKB-UHFFFAOYSA-N
- Pubchem - triacetin
- Wikipedia - triacetin
The triglyceride 1,2,3-triacetoxypropane is more generally known as triacetin and glycerin triacetate. It is the triester of glycerol and acetylating agents, such as acetic acid and acetic anhydride. It is a colorless, viscous and odorless liquid.
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