Structure

Triacetin

CAS
102-76-1
Catalog Number
ACM102761-1
Category
Inhibitors
Molecular Weight
218.2
Molecular Formula
C9H14O6

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Specification

Description
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.
Synonyms
1,3-Diacetyloxypropan-2-yl acetate
IUPAC Name
2,3-Diacetyloxypropyl acetate
Canonical SMILES
CC(=O)OCC(COC(=O)C)OC(=O)C
InChI
InChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3
InChI Key
URAYPUMNDPQOKB-UHFFFAOYSA-N
Boiling Point
258-260 °C(lit.)
Melting Point
3 °C(lit.)
Flash Point
300 °F
Density
1.16 g/mL at 25 °C(lit.)
Solubility
Moderately soluble in water, soluble in organic solvents
Appearance
Clear colorless liquid
Application
Triacetin serves a versatile role across multiple industries primarily due to its unique chemical properties. It is a triglyceride formed by the acetylation of glycerol's three hydroxy groups, resulting in a colorless, viscous liquid with a slightly fatty odor. Known chemically as glyceryl triacetate, triacetin is predominantly employed as a hydrophilic plasticizer in the coating of capsules, tablets, beads, and granules, enhancing the flexibility and durability of these materials. Moreover, it finds application in cosmetics, perfumery, and the food industry as an effective solvent and fixative for perfumes and flavors. Triacetin also exhibits fungistatic properties because it releases acetic acid upon hydrolysis by skin esterases, which makes it useful in treating minor dermatophyte infections. This release of acetic acid, while beneficial, is self-limiting due to the inhibition of these enzymes at lower pH levels. Through its multifaceted functionality, triacetin effectively contributes to various formulations, offering enhanced performance and stability.
Storage
Sealed in dry, room temperature
Active Content
95%
Autoignition Temperature
812 °F (433 °C);433 °C
Color/Form
Colorless liquid;Colorless somewhat oily liquid
Complexity
229
Covalently-Bonded Unit Count
1
Decomposition
When heated to decomposition it emits acrid smoke and irritating fumes.
EC Number
203-051-9;203-051-9
Exact Mass
218.07903816
Formal Charge
0
H-Bond Acceptor
6
H-Bond Donor
0
Heavy Atom Count
15
HS Code
2915390090
ICSC Number
1203
LogP
0.04430
MDL Number
MFCD00008716
Monoisotopic Mass
218.07903816
NSC Number
757364;4796
Odor
Slightly fatty odor
Other Experimental
Bulk density: 9.7 lb/gal;VP: 1 mm Hg at 100 °C;Henry's Law constant = 1.2X10-8 at 25 °C atm-cu m/mole at 25 °C (est);Hydroxyl radical reaction rate constant = 8.5X10-12 cu cm/mole-sec at 25 °C (est)
Physical State
Liquid
PSA
78.9
Refractive Index
n25/D 1.429-1.431(lit.)
Rotatable Bond Count
8
RTECS Number
AK3675000
Stability
Stable. Incompatible with strong oxidizing agents. Combustible.
Storage Conditions
Dry place,Room Temperature
Topological Polar Surface Area
78.9 Ų
UNII
XHX3C3X673
Vapor Density
7.52
Vapor Pressure
0.0141mmHg at 25°C
WGK Germany
1
XLogP3
0.2
What is the molecular weight of Triacetin?

The molecular weight of Triacetin is 218.2.

What is the IUPAC name of Triacetin?

The IUPAC name of Triacetin is 2,3-Diacetyloxypropyl acetate.

What is the boiling point of Triacetin?

The boiling point of Triacetin is 258-260 °C.

What is the melting point of Triacetin?

The melting point of Triacetin is 3°C.

What is the appearance of Triacetin?

Triacetin appears as a clear transparent oily liquid with a bitter taste.

What are some typical applications of Triacetin?

Some typical applications of Triacetin include use as a dispersing agent, emulsion stabilizer, plasticizer, and solvent.

What is the purity of Triacetin?

The purity of Triacetin is 95%+.

What is the density of Triacetin at 25°C?

The density of Triacetin is 1.16 g/mL at 25°C.

What is the CAS number of Triacetin?

The CAS number of Triacetin is 102-76-1.

What are some synonyms for Triacetin?

Some synonyms for Triacetin are Glyceryl triacetate and 1,2,3-triacetoxypropane.

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