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H1006

Sigma-Aldrich

Heptafluorobutyric anhydride

≥98%

Synonym(s):

HFAA, HFBA, Perfluorobutyric anhydride

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About This Item

Linear Formula:
(CF3CF2CF2CO)2O
CAS Number:
336-59-4
Molecular Weight:
410.06
Beilstein:
856036
EC Number:
206-410-8
MDL number:
MFCD00000432
UNSPSC Code:
12352100
PubChem Substance ID:
57654226
NACRES:
NA.22

Quality Level

100

Assay

≥98%

form

liquid

refractive index

n20/D 1.287 (lit.)

bp

108-110 °C (lit.)

mp

−43 °C (lit.)

density

1.674 g/mL at 20 °C (lit.)

storage temp.

room temp

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(=O)OC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8F14O3/c9-3(10,5(13,14)7(17,18)19)1(23)25-2(24)4(11,12)6(15,16)8(20,21)22

InChI key

UFFSXJKVKBQEHC-UHFFFAOYSA-N

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Application

Heptafluorobutyric anhydride can be used as a derivatizing agent for the determination of:
  • Alkylphenol ethoxylates and brominated flame retardants in sewage sludge samples.
  • Free amino acids in sugarcane by GC analysis.

Packaging

5ML and 25ML in glass bottle

10 AMP in ampule

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive 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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL0912
BCCM2961
BCCM2958
BCCL6123
BCCG8837

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An integrated method for the simultaneous determination of alkylphenol ethoxylates and brominated flame retardants in sewage sludge samples by ultrasonic-assisted extraction, solid phase clean-up, and GC-MS analysis
Chokwe T, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 123, 230-236 (2015)
C Fakt et al.
Journal of chromatography. B, Biomedical sciences and applications, 700(1-2), 93-100 (1997-12-09)
A convenient and sensitive method for the quantitative determination of poly(ethylene glycol) 400 in plasma and urine with capillary gas chromatography-mass spectrometry has been developed. The sample preparation involves solid-phase extraction with subsequent derivatization with heptafluorobutyric anhydride, which proved to
H J Helmlin et al.
Journal of analytical toxicology, 20(6), 432-440 (1996-10-01)
In Europe, the compound 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy, Adam), in addition to cannabis, is the most abused illicit drug at all-night "techno" parties. Methods for the determination of MDMA and its metabolites, 4-hydroxy-3-methoxymethamphetamine (HMMA), 3,4-dihydroxy-methamphetamine (HHMA), 3,4-methylenedioxyamphetamine (MDA), 4-hydroxy-3-methoxyamphetamine (HMA), and
A Fidder et al.
Chemical research in toxicology, 9(4), 788-792 (1996-06-01)
We report that exposure to the chemical warfare agent sulfur mustard can be monitored by means of a modified Edman degradation involving selective release of the N-terminal valine adduct of hemoglobin with the agent. The degree of alkylation of the
J K Mensah et al.
Journal of chromatography. A, 765(1), 85-90 (1997-03-21)
A method for the determination of residues of the insecticide diflubenzuron, 1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)urea, in apples using gas chromatography with electron-capture detection has been developed and validated. The three solvents ethyl acetate, acetone and dichloromethane were tested for extraction of diflubenzuron residues
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