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About This Item
Empirical Formula (Hill Notation):
C7H3F7N2O
CAS Number:
Molecular Weight:
264.10
UNSPSC Code:
12352005
NACRES:
NA.32
PubChem Substance ID:
EC Number:
251-063-8
Beilstein/REAXYS Number:
4488026
MDL number:
InChI key
MSYHGYDAVLDKCE-UHFFFAOYSA-N
InChI
1S/C7H3F7N2O/c8-5(9,6(10,11)7(12,13)14)4(17)16-2-1-15-3-16/h1-3H
SMILES string
FC(F)(F)C(F)(F)C(F)(F)C(=O)n1ccnc1
product line
BioReagent
bp
158-163 °C (lit.)
suitability
suitable for derivatization
storage temp.
−20°C
Quality Level
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General description
1-(Heptafluorobutyryl)imidazole, also known as HFBI, is an acylating derivatization reagent. It is a mild amine-group derivatizing agent. HFBI doesn’t produce acidic by-products in reaction, and the unutilized reagent doesn’t damage the chromatographic process. Post derivatization reaction, the HFB (Heptafluorobutyryl) derivatives are analyzed chromatographically.
Application
1-(Heptafluorobutyryl)imidazole is used as a derivatizing agent for analysing Sulphur mustard metabolites. It is suitable to study dispersive derivatization of degradation products.
Biochem/physiol Actions
Mild amine-group derivatizing reagent; non-acidic by-product prevents decomposition and reduces GC column degradation.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
170.6 °F - closed cup
flash_point_c
77 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Meehir Palit et al.
Journal of chromatography. A, 1218(32), 5393-5400 (2011-07-09)
A new derivatization and extraction technique termed as dispersive derivatization liquid-liquid extraction (DDLLE) speeds up the analysis process by removing the requirement for drying of the sample. The derivatization process takes place at the interface between the analyte containing aqueous
Minjia Huang et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 21(11), 1343-1347 (2005-12-02)
Headspace solid-phase microextraction (HS-SPME) coupled with gas chromatography/mass spectrometry (GC/MS) method was developed to determine 3-chloropropane-1,2-diol (3-MCPD) in hydrolyzed vegetable protein and Chinese soy sauce. The 3-MCPD was firstly derivativized with phenylboronic acid in aqueous solution at 90 degrees C
The use of tandem mass spectrometry for the identification and quantitation of tryptolines (tetrahydro-beta-carbolines) in tissue extracts.
J V Johnson et al.
Progress in clinical and biological research, 183, 161-177 (1985-01-01)
Zhiyong Nie et al.
Talanta, 85(2), 1154-1159 (2011-07-06)
The N-terminal valine adduct (HETE-Val) in globin is believed to behave as a long-lived biomarker after exposure to sulfur mustard (HD). Development of a highly sensitive method for monitoring HETE-Val, particularly at low HD exposure levels or for retrospective detection
Jussi J Joensuu et al.
Methods in molecular biology (Clifton, N.J.), 824, 527-534 (2011-12-14)
Two main hurdles hinder the widespread acceptance of plants as a preferred protein expression platform: low accumulation levels and expensive chromatographic purification methods. Fusion of proteins of interest to fungal hydrophobins has provided a tool to address both accumulation and
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