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139238

Sigma-Aldrich

Hexafluoroacetone trihydrate

98%

Synonym(s):

Hexafluoro-2-propanone trihydrate, Perfluoroacetone trihydrate

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About This Item

Linear Formula:
(CF3)2CO · 3H2O
CAS Number:
34202-69-2
Molecular Weight:
220.07
Beilstein:
607236
EC Number:
211-676-3
MDL number:
MFCD00149061
UNSPSC Code:
12352100
PubChem Substance ID:
24848398
NACRES:
NA.22

vapor pressure

87.5 psi ( 21 °C)

Assay

98%

form

liquid

refractive index

n20/D 1.319 (lit.)

mp

18-21 °C (lit.)

density

1.579 g/mL at 25 °C (lit.)

SMILES string

[H]O[H].[H]O[H].[H]O[H].FC(F)(F)C(=O)C(F)(F)F

InChI

1S/C3F6O.3H2O/c4-2(5,6)1(10)3(7,8)9;;;/h;3*1H2

InChI key

SNZAEUWCEHDROX-UHFFFAOYSA-N

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General description

Hexafluoroacetone trihydrate forms crystalline 1:1 complexes with imidazole 3-oxides.

Application

Hexafluoroacetone trihydrate was used to study the kinetics and thermodynamics of linkage isomerization of (acetone)pentaammineruthenium (III) and-ruthenium (II) complexes. It was used in a study to reconstitute the α-and β-polypeptides of both Rhodobacter sphaeroides and Rhodospirillum rubrum with bacteriochlorophyll a.

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Hexachloro-2-propanone 99%

Sigma-Aldrich

H5308

Hexachloro-2-propanone

C M Davis et al.
The Journal of biological chemistry, 270(11), 5793-5804 (1995-03-17)
Methodology has been developed to reconstitute carotenoids and bacteriochlorophyll alpha with isolated light-harvesting complex I (LHI) polypeptides of both Rhodobacter sphaeroides and Rhodospirillum rubrum. Reconstitution techniques first developed in this laboratory using the LHI polypeptides of R. rubrum, R. sphaeroides
First synthesis of the N (1)-bulky substituted imidazole 3-oxides and their complexation with hexafluoroacetone hydrate.
Mloston G and Jasinski M.
ARKIVOC (Gainesville, FL, United States), 6, 162-175 (2011)
Linkage isomerization reactions of (acetone) pentaammineruthenium (III) and-ruthenium (II) complexes.
Powell DW and Lay PA.
Inorganic Chemistry, 31(17), 3542-3550 (1992)
Diwakar M Pawar et al.
The Journal of organic chemistry, 72(6), 2003-2007 (2007-02-17)
Low-temperature 1H and 13C NMR spectra of formic acid (1) showed separate signals for the E and Z conformations in solvents containing a hydrogen bond acceptor, dimethyl ether. The population of E-1 (6.2% in 3:1:1 CHClF2/CHCl2F/(CH3)2O) was larger than that
T Rühl et al.
Amino acids, 27(3-4), 285-290 (2004-11-19)
Hexafluoroacetone was applied as a bidentate protecting and activating agent for the syntheses of RGD-peptide mimetics starting from iminodiacetic acid in solution and on solid phase.
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