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tert-Butyl peroxyacetate

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tert-Butyl peroxyacetate Basic information

Product Name:
tert-Butyl peroxyacetate
Synonyms:
  • Ethaneperoxoicacid,1,1-dimethylethylester
  • T-BUTYL PERACETATE
  • TERT-BUTYL PERACETATE
  • TERT-BUTYL PEROXYACETATE
  • Butylperacetate
  • tert-Butyl peracetate solution
  • Trigonox?F
  • TERT-BUTYL PERACETATE 75 WT. % SOLUTIO&
CAS:
107-71-1
MF:
C6H12O3
MW:
132.16
EINECS:
203-514-5
Product Categories:
  • Organics
  • Free Radical Initiators
  • Organic Peroxides
  • Polymerization Initiators
Mol File:
107-71-1.mol
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tert-Butyl peroxyacetate Chemical Properties

Melting point:
-20 °C
Boiling point:
184.08°C (rough estimate)
Density 
0.828 g/mL at 25 °C
vapor pressure 
1.966Pa at 25℃
refractive index 
n20/D 1.412
Flash point:
99 °F
storage temp. 
Refrigerator (+4°C) + Flammables area
form 
Solution
color 
Clear
Water Solubility 
3.878g/L at 25℃
InChI
InChI=1S/C6H12O3/c1-5(7)8-9-6(2,3)4/h1-4H3
InChIKey
SWAXTRYEYUTSAP-UHFFFAOYSA-N
SMILES
C(OOC(C)(C)C)(=O)C
LogP
1.6 at 25℃
CAS DataBase Reference
107-71-1(CAS DataBase Reference)
EPA Substance Registry System
tert-Butyl peroxyacetate (107-71-1)
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Safety Information

Hazard Codes 
F,T,O,Xi
Risk Statements 
23/24/25-36/37/38-40-65-22-10-7-45-46
Safety Statements 
16-26-36/37/39-45-62-47-14-7-53-3/7-36/37-35
RIDADR 
UN 3103 5.2
WGK Germany 
2
RTECS 
SD8925000
HazardClass 
5.2
PackingGroup 
II
HS Code 
29159000

MSDS

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tert-Butyl peroxyacetate Usage And Synthesis

Chemical Properties

clear solution

Uses

It is used to initiate polymerization, and inorganic syntheses.

Uses

Allows the direct copper catalyzed acetoxylation of β-lactams at the 4-position.

Uses

Polymerization initiator for vinyl monomers, manufacture of polyethylene and polystyrene.

General Description

tert-Butyl peroxyacetate is sensitive to heat. Storage of tert-Butyl peroxyacetate must be done so with stringent temperature control measures. It's explosion hazard is also mitigated by mixing the peroxide with an inert solid.

Reactivity Profile

tert-Butyl peroxyacetate explodes with great violence when rapidly heated to a critical temperature; pure form is shock sensitive and detonable [Bretherick 1979 p. 602]. Upon contact with organic matter, t-butyl peroxyacetate can ignite or give rise to an explosion [Haz. Chem. Data 1973 p. 77].

Hazard

Flammable, dangerous fire risk. Oxidizer.

Health Hazard

Mild skin and eye irritant. Its toxicity is low,both via inhalation and ingestion routes.
LD50 value, oral (rats): 675 mg/kg.

Fire Hazard

The pure compound is highly reactive and oxidizing, and sensitive to heat and shock.
A 75% solution in benzene or mineral spirits is the maximum assay that is sold commercially. Its benzene solution at this concentration is reactive, oxidizing, and flammable. The flash point varies depending on the solvent; the autoignition temperature not reported; the self-accelerating decomposition temperature is 93°C (199.4°F).
t-Butyl peroxyacetate forms an explosive mixture with air, explosive range not reported. It can ignite or explode when in contact with combustible organic compounds. Fire-extinguishing agent: water from a sprinkler from an explosion-resistant location; keep the containers cool.

Flammability and Explosibility

Flammable

Safety Profile

Moderately toxic by ingestion. Mildly toxic by inhalation. Moderate skin and eye irritant. A shockand heat-sensitive explosive. Dangerous fire hazard when exposed to heat, flame, reducing agents. To fight fire, use dry chemical, alcohol foam, spray and mist. When heated to decomposition it emits acrid smoke and fumes. See also PEROXIDES, ORGANIC; and ESTERS

storage

Store in a cool and well-ventilated placeisolated from other chemicals; protect fromphysical damage. It is shipped in glass andearthenware containers not exceeding 7 lb,inside a wooden or fiberboard box.

Purification Methods

Wash the ester with NaHCO3 from a *benzene solution, then redistil to remove *benzene [Kochi J Am Chem Soc 84 774 1962]. Handle with adequate protection due to possible EXPLOSIVE nature. [Beilstein 2 IV 391.]

References

[1] J. Wenzel, Sunggyu Lee. “Tert-butyl peroxyacetate initiated semibatch polymerization of 1,1-difluoroethylene in supercritical carbon dioxide.” Polymer Engineering and Science 16 1 (2016): 435–440.
[2] V. A. Donchak, R. S. Yur'ev, S. A. Voronov. “New synthesis of tert-butyl peroxycarboxylates.” Russian Journal of Organic Chemistry 42 4 (2006): 487–490.

tert-Butyl peroxyacetate Preparation Products And Raw materials

Raw materials

Preparation Products

tert-Butyl peroxyacetateSupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
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021-61259108 18621169109
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Shandong Xiya Chemical Co., Ltd
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4009903999 13355009207
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Tianjin heowns Biochemical Technology Co., Ltd.
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400 638 7771
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Maya High Purity Chemicals
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+86 (573) 82222445 (0)18006601000 452520369
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Thermo Fisher Scientific
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800-810-5118
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cnchemical@thermofisher.com